WO2019186733A1 - Wavelength conversion member, backlight unit, image display device and curable composition - Google Patents

Wavelength conversion member, backlight unit, image display device and curable composition Download PDF

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Publication number
WO2019186733A1
WO2019186733A1 PCT/JP2018/012588 JP2018012588W WO2019186733A1 WO 2019186733 A1 WO2019186733 A1 WO 2019186733A1 JP 2018012588 W JP2018012588 W JP 2018012588W WO 2019186733 A1 WO2019186733 A1 WO 2019186733A1
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WIPO (PCT)
Prior art keywords
curable composition
wavelength conversion
conversion member
cured product
quantum dot
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PCT/JP2018/012588
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French (fr)
Japanese (ja)
Inventor
達也 矢羽田
国廣 桐ケ谷
康平 向垣内
美香 柳田
Original Assignee
日立化成株式会社
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Application filed by 日立化成株式会社 filed Critical 日立化成株式会社
Priority to PCT/JP2018/012588 priority Critical patent/WO2019186733A1/en
Priority to PCT/JP2019/013419 priority patent/WO2019189498A1/en
Priority to JP2019551712A priority patent/JP6702515B2/en
Publication of WO2019186733A1 publication Critical patent/WO2019186733A1/en
Priority to JP2020080791A priority patent/JP2020170164A/en

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    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/20—Filters
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
    • H01L33/48—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor body packages
    • H01L33/50—Wavelength conversion elements

Definitions

  • the present invention relates to a wavelength conversion member, a backlight unit, an image display device, and a curable composition.
  • the wavelength conversion member including the quantum dot phosphor is disposed, for example, in the backlight unit of the image display device.
  • a wavelength conversion member including a quantum dot phosphor that emits red light and a quantum dot phosphor that emits green light when the wavelength conversion member is irradiated with blue light as excitation light, the quantum dot phosphor emits light.
  • White light can be obtained by the red light and green light that have been generated and the blue light that has passed through the wavelength conversion member.
  • the wavelength conversion member containing the quantum dot phosphor usually has a cured product obtained by curing a curable composition containing the quantum dot phosphor.
  • the curable composition includes a thermosetting type and a photocurable type, and a photocurable type curable composition is preferably used from the viewpoint of productivity.
  • the wavelength conversion member containing quantum dot fluorescent substance at least one part of the hardened
  • a barrier film having a barrier property against oxygen may be provided on one side or both sides of a cured product containing a quantum dot phosphor.
  • the quantum dot phosphor in the cured product is likely to deteriorate due to the influence of oxygen. Therefore, when the wavelength conversion member containing the quantum dot phosphor is left in a high-temperature and high-humidity environment, the quantum dot phosphor may deteriorate and the emission intensity may decrease.
  • a cured product of a photocurable curable composition containing a quantum dot phosphor has insufficient durability (moisture and heat resistance) in a high-temperature and high-humidity environment, and the quantum dot phosphor is deteriorated and has a light emission intensity. It tends to decrease.
  • the present disclosure has been made in view of the above circumstances, and an object of the present disclosure is to provide a wavelength conversion member that includes a quantum dot phosphor and is excellent in moisture and heat resistance, a backlight unit using the same, and an image display device. Furthermore, this indication aims at providing the curable composition which can form the hardened
  • a wavelength conversion member comprising a cured product including a quantum dot phosphor and having an alkyleneoxy structure.
  • the quantum dot phosphor includes a compound containing at least one of Cd and In.
  • ⁇ 5> The polar component calculated from the formula of Wu using the contact angle of diiodomethane and the contact angle of water in the cured product is 5 mJ / m 2 to 12 mJ / m 2 , from ⁇ 1> to ⁇ 4>
  • ⁇ 7> The wavelength conversion member according to any one of ⁇ 1> to ⁇ 6>, wherein a glass transition temperature of the cured product measured by dynamic viscoelasticity measurement is 47 ° C. or lower.
  • a backlight unit comprising the wavelength conversion member according to any one of ⁇ 1> to ⁇ 7> and a light source.
  • An image display device comprising the backlight unit according to ⁇ 8>.
  • a curable composition comprising a quantum dot phosphor, an alkyleneoxy group-containing compound having an alkyleneoxy group and a polymerizable reactive group, and a photopolymerization initiator.
  • the curable composition according to ⁇ 10> further comprising a polyfunctional thiol compound.
  • the ratio of the number of thiol groups in the polyfunctional thiol compound to the number of polymerizable reactive groups in the alkyleneoxy group-containing compound is 0.5 to
  • ⁇ 15> The curable composition according to any one of ⁇ 10> to ⁇ 14>, wherein the polymerizable reactive group includes a (meth) acryloyl group.
  • the polymerizable reactive group includes a (meth) acryloyl group.
  • ⁇ 16> The curable composition according to any one of ⁇ 10> to ⁇ 15>, further comprising a carboxylic acid having 1 to 17 carbon atoms.
  • ⁇ 17> The curable composition according to any one of ⁇ 10> to ⁇ 16>, further comprising a white pigment.
  • a wavelength conversion member that includes a quantum dot phosphor and is excellent in moisture and heat resistance
  • a backlight unit and an image display device using the wavelength conversion member Furthermore, according to the present disclosure, it is possible to provide a curable composition capable of forming a cured product that includes a quantum dot phosphor and is excellent in moisture and heat resistance.
  • each component may contain a plurality of corresponding substances.
  • the content or content of each component is the total content or content of the multiple types of substances present in the composition unless otherwise specified.
  • a plurality of particles corresponding to each component may be included.
  • the particle diameter of each component means a value for a mixture of the plurality of particles present in the composition unless otherwise specified.
  • the term “layer” or “film” includes only a part of the region in addition to the case where the layer or film is formed over the entire region. The case where it is formed is also included.
  • laminate indicates that layers are stacked, and two or more layers may be combined, or two or more layers may be detachable.
  • (meth) acryloyl means at least one of acryloyl and methacryloyl
  • (meth) acrylate means at least one of acrylate and methacrylate
  • “(meth) allyl” means allyl and methallyl. Means at least one.
  • a compound containing both a thiol group and an alkyleneoxy group is classified as a thiol compound.
  • a structure in which an oxygen atom of an ester bond and a carbon atom adjacent to the oxygen atom are bonded (—O—R in —C ( ⁇ O) —O—R, R represents a substituent)
  • a structure in which an oxygen atom of a hydroxyl group and a carbon atom adjacent to the oxygen atom are bonded is not classified as an alkyleneoxy group.
  • the wavelength conversion member of the present disclosure includes a cured product including a quantum dot phosphor and having an alkyleneoxy structure.
  • the wavelength conversion member of the present disclosure may include other components such as a coating material to be described later as necessary.
  • the cured product of the present disclosure may be a cured product of the curable composition of the present disclosure described later.
  • the wavelength conversion member of the present disclosure is suitably used for image display.
  • the wavelength conversion member of the present disclosure has improved relative emission intensity retention, which is an indicator of deterioration of the quantum dot phosphor, even when exposed to a high temperature and high humidity environment because the cured product has an alkyleneoxy structure. And excellent in heat and humidity resistance. This is because polarity is imparted to the cured product by the alkyleneoxy structure, and nonpolar oxygen is difficult to dissolve in components (eg, resin components) in the cured product, so that it is difficult for oxygen to contact the quantum dot phosphor. Thus, the reason is that the oxidative deterioration of the quantum dots is suppressed.
  • the alkyleneoxy structure may be derived, for example, from an alkyleneoxy group in an alkyleneoxy group-containing compound contained in the curable composition described later.
  • the component in the cured product has an alkyleneoxy structure
  • the compatibility between the component in the cured product and the quantum dot phosphor is reduced, and the cured product is likely to become cloudy, thus providing a light scattering effect to the cured product. Tend to be.
  • the oxidative deterioration of the quantum dot phosphor is suitably suppressed, even if the content of the quantum dot phosphor in the cured product is reduced as compared with the conventional case, a good emission intensity is obtained. It tends to be obtained.
  • the cured product preferably has a sulfide structure.
  • the sulfide structure is, for example, a compound containing a thiol group in a polyfunctional thiol compound that can be included in the curable composition described later and a polymerizable reactive group such as a carbon-carbon double bond (for example, an alkyleneoxy group containing described later) It may be formed by a polymerization reaction with a polymerizable reactive group in the compound).
  • the cured product may have an alicyclic structure.
  • the alicyclic structure contained in the cured product is not particularly limited. Specific examples of the alicyclic structure include a tricyclodecane skeleton, a cyclohexane skeleton, a 1,3-adamantane skeleton, a hydrogenated bisphenol A skeleton, a hydrogenated bisphenol F skeleton, a hydrogenated bisphenol S skeleton, and an isobornyl skeleton. Among these, a tricyclodecane skeleton or an isobornyl skeleton is preferable, and a tricyclodecane skeleton is more preferable.
  • the alicyclic structure contained in the cured product may be one type alone or at least two types.
  • examples of combinations of alicyclic structures include a combination of a tricyclodecane skeleton and an isobornyl skeleton, a combination of a hydrogenated bisphenol A skeleton and an isobornyl skeleton, and the like.
  • a combination of a tricyclodecane skeleton and an isobornyl skeleton is preferable.
  • the cured product may have an ester structure.
  • the ester structure may be derived from, for example, an ester structure in an alkyleneoxy group-containing compound contained in the curable composition described later.
  • the wavelength conversion member of the present disclosure uses the contact angle of diiodomethane and the contact angle of water in the cured product, and the polar component calculated from the Wu equation is preferably 5 mJ / m 2 to 12 mJ / m 2 .
  • the polar component calculated from the Wu equation is preferably 5 mJ / m 2 to 12 mJ / m 2 .
  • Polar components described above, from the viewpoint of further excellent wet heat resistance is preferably 5.5mJ / m 2 ⁇ 11mJ / m 2, more preferably from 6.0mJ / m 2 ⁇ 10.5mJ / m 2 6.0 mJ / m 2 to 10 mJ / m 2 is more preferable.
  • the wavelength conversion member of the present disclosure preferably has a moisture permeability of 20 g / m 2 ⁇ day or more under the conditions of a temperature of 40 ° C. and a relative humidity of 70%. Since the moisture permeability mentioned above is a certain value or more, the cured product has high polarity, and non-polar oxygen is not easily dissolved in the components in the cured product. There is a tendency that oxidative deterioration of the quantum dot phosphor in the cured product is suitably suppressed.
  • a cured product having a moisture permeability of a certain value or more is likely to adsorb moisture, and by adsorbing moisture, the polarity of the cured product becomes higher, and nonpolar oxygen is less likely to be dissolved by components in the cured product. Therefore, it is presumed that the oxidative deterioration of the quantum dot phosphor is suitably suppressed.
  • the moisture permeability of the cured product under the conditions of a temperature of 40 ° C. and a relative humidity of 70% can be measured according to the measurement method of JIS Z 0208: 1976 as described in the examples described later.
  • the above-mentioned moisture permeability is more preferably 30 g / m 2 ⁇ day or more, further preferably 40 g / m 2 ⁇ day or more, more preferably 50 g / m 2 ⁇ day or more, from the viewpoint that the decrease in emission intensity is more suitably suppressed.
  • m is 2 ⁇ day or more, and still more preferably 60 g / m 2 ⁇ day or more.
  • the moisture permeability is preferably 250 g / m 2 ⁇ day or less, more preferably 210 g / m 2 ⁇ day or less, from the viewpoint of suppressing an increase in oxygen permeability due to a decrease in cohesive strength of the cured product. More preferably, it is more preferably 180 g / m 2 ⁇ day or less, and particularly preferably 150 g / m 2 ⁇ day or less.
  • a ratio (V1 /) of a peak area (V1) attributed to C C stretching vibration and a peak area (V2) attributed to SH stretching vibration in a cured product.
  • V2) is preferably 0.00052 or less, more preferably 0.0001 or less, and further preferably 0.00009 or less.
  • the ratio (V1 / V2) may be 0.00001 or more, 0.00003 or more, or 0.00004 or more.
  • the glass transition temperature of the cured product tends to decrease, so the oxygen permeability tends to increase due to the reduced cohesive strength of the cured product. It tends to be excellent in workability.
  • the background measurement is performed with air, and FT-IR measurement is performed under the condition of 16 integrations.
  • the wavelength conversion member has a coating material
  • the cured product of the wavelength conversion member in a state where the coating material is peeled is subjected to FT-IR measurement.
  • the cured product may contain a white pigment.
  • the details of the white pigment contained in the cured product are as described in the section of the curable composition described later.
  • the details of the quantum dot phosphor contained in the cured product are also as described in the section of the curable composition described later.
  • the shape of the wavelength conversion member is not particularly limited, and examples thereof include a film shape and a lens shape.
  • the wavelength conversion member is preferably a film.
  • the average thickness of the cured product is, for example, preferably 50 ⁇ m to 200 ⁇ m, more preferably 50 ⁇ m to 150 ⁇ m, and even more preferably 80 ⁇ m to 120 ⁇ m.
  • the average thickness is 50 ⁇ m or more, the wavelength conversion efficiency tends to be further improved, and when the average thickness is 200 ⁇ m or less, the backlight unit tends to be thinner when applied to the backlight unit described later. is there.
  • the average thickness of the film-like cured product is, for example, as an arithmetic average value of thicknesses measured at arbitrary three locations using a micrometer or by observing a cross section of the cured product using an SEM (scanning electron microscope). Desired.
  • the average thickness (for example, average thickness of coating
  • the average thickness of the wavelength conversion member other than the cured product may be subtracted from the average thickness of the wavelength conversion member.
  • cured material uses a reflection spectral film thickness meter etc., or hardened
  • the wavelength conversion member may be one obtained by curing one type of curable composition, or may be one obtained by curing two or more types of curable compositions.
  • the wavelength conversion member when the wavelength conversion member is in the form of a film, the wavelength conversion member emits light from the first cured product obtained by curing the curable composition containing the first quantum dot phosphor and the first quantum dot phosphor.
  • a laminate of a second cured product obtained by curing a curable composition containing second quantum dot phosphors having different characteristics may be used.
  • the wavelength conversion member can be obtained by irradiating an active energy ray such as an ultraviolet ray after forming a coating film, a molded product or the like of the curable composition and performing a drying treatment as necessary.
  • the wavelength and irradiation amount of the active energy ray can be appropriately set according to the composition of the curable composition. In one aspect, it is irradiated with ultraviolet rays having a wavelength of 280 nm ⁇ 400 nm at an irradiation amount of 100mJ / cm 2 ⁇ 5000mJ / cm 2.
  • Examples of the ultraviolet light source include a low-pressure mercury lamp, a medium-pressure mercury lamp, a high-pressure mercury lamp, an ultrahigh-pressure mercury lamp, a carbon arc lamp, a metal halide lamp, a xenon lamp, a chemical lamp, a black light lamp, and a microwave-excited mercury lamp.
  • the cured product preferably has a glass transition temperature (Tg) of 47 ° C. or lower, more preferably 0 ° C. to 47 ° C., and more preferably 10 ° C. to 47 ° C. from the viewpoint of further improving adhesion and workability. More preferably, the temperature is 15 ° C. to 21 ° C.
  • the glass transition temperature (Tg) of the cured product can be measured using a dynamic viscoelasticity measuring device (for example, Rheometric Scientific, Solid Analyzer RSA-III) under the condition of a frequency of 10 Hz.
  • the cured product preferably has a storage elastic modulus of 1 ⁇ 10 3 Pa to 1 ⁇ 10 10 Pa measured under conditions of a frequency of 10 Hz and a temperature of 25 ° C. from the viewpoint of improving adhesion and heat resistance. More preferably, it is from x10 4 Pa to 1 x 10 9 Pa, and even more preferably from 1 x 10 5 Pa to 1 x 10 7 Pa.
  • the storage elastic modulus of the cured product can be measured using a dynamic viscoelasticity measuring device (for example, Rheometric Scientific, Solid Analyzer RSA-III).
  • the wavelength conversion member of the present disclosure may further include a covering material that covers at least a part of the cured product.
  • a covering material that covers at least a part of the cured product.
  • the cured product is in the form of a film
  • one side or both sides of the film-like cured product may be covered with a film-shaped coating material.
  • the coating material has a barrier property against oxygen from the viewpoint of suppressing a decrease in light emission efficiency of the quantum dot phosphor.
  • the wavelength conversion member of the present disclosure is considered that the cured product has high polarity and nonpolar oxygen is hardly dissolved in a component (for example, a resin component) in the cured product, an inorganic layer described later is provided.
  • coated material with a barrier property with respect to oxygen lower than the barrier film to have may be sufficient.
  • the material of the coating material is not particularly limited.
  • resin is mentioned.
  • the type of resin is not particularly limited, polyester such as polyethylene terephthalate (PET) and polyethylene naphthalate (PEN), polyolefin such as polyethylene (PE) and polypropylene (PP), polyamide such as nylon, and ethylene-vinyl alcohol copolymer (EVOH) and the like.
  • the covering material may be one (barrier film) provided with a barrier layer for enhancing the barrier function.
  • the barrier layer include inorganic layers containing inorganic substances such as alumina and silica.
  • the covering material may be a single layer structure or a multilayer structure. In the case of a multilayer structure, a combination of two or more layers having different materials may be used.
  • the average thickness of the coating material is, for example, preferably 80 ⁇ m to 150 ⁇ m, more preferably 100 ⁇ m to 140 ⁇ m, and even more preferably 100 ⁇ m to 135 ⁇ m.
  • the average thickness is 80 ⁇ m or more, functions such as barrier properties tend to be sufficient, and when the average thickness is 150 ⁇ m or less, a decrease in light transmittance tends to be suppressed.
  • the average thickness of the film-shaped coating material is obtained in the same manner as the average thickness of the film-shaped wavelength conversion member.
  • the coating material preferably contains EVOH.
  • the coating material containing EVOH tends to be inferior to the water barrier property than the barrier film composed of the resin base material and the inorganic layer, but suppresses deterioration of the quantum dot phosphor because the oxygen permeability is particularly low among the resins. It has a sufficient oxygen barrier property.
  • the proportion of ethylene-derived structural units (ethylene content) in EVOH is not particularly limited, and can be selected in consideration of the desired characteristics of the wavelength conversion member. From the viewpoint of oxygen barrier properties, the ethylene content is preferably small, and from the viewpoint of strength and water resistance, the ethylene content is preferably large.
  • the ethylene content in EVOH is preferably 20 mol% to 50 mol%, more preferably 25 mol% to 45 mol%, and even more preferably 30 mol% to 40 mol%.
  • the average thickness of the covering material containing EVOH is, for example, preferably 20 ⁇ m or more, and more preferably 50 ⁇ m or more. When the average thickness is 20 ⁇ m or more, functions such as barrier properties tend to be sufficient.
  • the average thickness of the covering material containing EVOH is, for example, preferably 150 ⁇ m or less, and more preferably 125 ⁇ m or less. When the average thickness is 150 ⁇ m or less, a decrease in light transmittance tends to be suppressed.
  • the oxygen permeability of the covering material is, for example, preferably 0.5 cm 3 / (m 2 ⁇ day ⁇ atm) or less, and more preferably 0.3 cm 3 / (m 2 ⁇ day ⁇ atm) or less. More preferably, it is 0.1 cm 3 / (m 2 ⁇ day ⁇ atm) or less.
  • the oxygen permeability of the coating material can be measured under the conditions of 20 ° C. and 65% relative humidity using an oxygen permeability measuring device (for example, MOCON, OX-TRAN).
  • an oxygen permeability measuring device for example, MOCON, OX-TRAN.
  • the upper limit value of the water vapor transmission rate of the coating material is not particularly limited, but may be, for example, 1 ⁇ 10 ⁇ 1 g / (m 2 ⁇ day) or less.
  • the water vapor transmission rate of the coating material can be measured in an environment of 40 ° C. and 90% relative humidity using a water vapor transmission rate measuring device (for example, MOCON, AQUATRAN).
  • a water vapor transmission rate measuring device for example, MOCON, AQUATRAN.
  • the wavelength conversion member of the present disclosure has a total light transmittance of preferably 55% or more, more preferably 60% or more, and more preferably 65% or more from the viewpoint of further improving the light utilization efficiency. Further preferred.
  • the total light transmittance of the wavelength conversion member can be measured in accordance with the measurement method of JIS K 7136: 2000.
  • the haze is preferably 95% or more, more preferably 97% or more, and further preferably 99% or more.
  • the haze of the wavelength conversion member can be measured in accordance with the measurement method of JIS K 7136: 2000.
  • the wavelength conversion member of the present disclosure is not limited to the configuration of FIG.
  • covering material is notional, and the relative relationship of a magnitude
  • symbol is attached
  • the 1 includes a cured product 11 that is a film-like cured product, and film-shaped coating materials 12A and 12B that are provided on both surfaces of the cured product 11.
  • the types and average thicknesses of the covering material 12A and the covering material 12B may be the same or different.
  • 1 can be manufactured by, for example, the following known manufacturing method.
  • a coating composition is formed by applying a curable composition described later to the surface of a film-like coating material (hereinafter also referred to as “first coating material”) that is continuously conveyed.
  • a method for applying the curable composition is not particularly limited, and examples thereof include a die coating method, a curtain coating method, an extrusion coating method, a rod coating method, and a roll coating method.
  • second coating material a film-like coating material that is continuously conveyed is bonded onto the coating film of the curable composition.
  • the coating film is cured to form a cured product.
  • the wavelength conversion member of the structure shown in FIG. 1 can be obtained by cutting out to a regular size.
  • the coating material is irradiated with active energy rays before the second coating material is bonded, and the cured product is removed. It may be formed.
  • the backlight unit of the present disclosure includes the above-described wavelength conversion member of the present disclosure and a light source.
  • the backlight unit is preferably a multi-wavelength light source from the viewpoint of improving color reproducibility.
  • blue light having an emission center wavelength in a wavelength range of 430 nm to 480 nm, an emission intensity peak having a half width of 100 nm or less, and an emission center wavelength in a wavelength range of 520 nm to 560 nm
  • the half-value width of the emission intensity peak means a peak width at half the peak height and a full width at half maximum (Full Width at Half Maximum, FWHM).
  • the emission center wavelength of the blue light emitted from the backlight unit is preferably in the range of 440 nm to 475 nm.
  • the emission center wavelength of the green light emitted from the backlight unit is preferably in the range of 520 nm to 545 nm.
  • the emission center wavelength of red light emitted from the backlight unit is preferably in the range of 610 nm to 640 nm.
  • the half-value widths of the emission intensity peaks of blue light, green light, and red light emitted by the backlight unit are all preferably 80 nm or less, and 50 nm or less. More preferably, it is more preferably 40 nm or less, particularly preferably 30 nm or less, and extremely preferably 25 nm or less.
  • the light source of the backlight unit for example, a light source that emits blue light having an emission center wavelength in a wavelength region of 430 nm to 480 nm can be used.
  • the light source include an LED (Light Emitting Diode) and a laser.
  • the wavelength conversion member preferably includes at least a quantum dot phosphor R that emits red light and a quantum dot phosphor G that emits green light. Thereby, white light can be obtained from the red light and green light emitted from the wavelength conversion member and the blue light transmitted through the wavelength conversion member.
  • the light source of the backlight unit for example, a light source that emits ultraviolet light having an emission center wavelength in a wavelength region of 300 nm to 430 nm can be used.
  • the light source include an LED and a laser.
  • the wavelength conversion member preferably includes a quantum dot phosphor B that emits blue light when excited by excitation light, together with the quantum dot phosphor R and the quantum dot phosphor G. Thereby, white light can be obtained from the red light, the green light, and the blue light emitted from the wavelength conversion member.
  • the backlight unit of the present disclosure may be an edge light type or a direct type.
  • FIG. 2 An example of a schematic configuration of an edge light type backlight unit is shown in FIG.
  • the backlight unit of the present disclosure is not limited to the configuration of FIG.
  • size of the member in FIG. 2 is notional, The relative relationship of the magnitude
  • the backlight unit 20 shown in FIG. 2 includes a light source 21 for emitting the blue light L B, a light guide plate 22 to be emitted guiding the blue light L B emitted from the light source 21, the light guide plate 22 and disposed to face A wavelength conversion member 10, a retroreflective member 23 disposed opposite to the light guide plate 22 via the wavelength conversion member 10, and a reflection plate 24 disposed opposite to the wavelength conversion member 10 via the light guide plate 22.
  • Wavelength conversion member 10 emits the red light L R and the green light L G part of the blue light L B as the excitation light, the red light L and R and the green light L G, the blue light was not the excitation light L B is emitted.
  • the red light L R, the green light L G, and the blue light L B, the white light L W is emitted from the retroreflective member 23.
  • An image display device includes the above-described backlight unit according to the present disclosure.
  • the image display device is not particularly limited, and examples thereof include a liquid crystal display device.
  • FIG. 3 An example of a schematic configuration of the liquid crystal display device is shown in FIG.
  • the liquid crystal display device of the present disclosure is not limited to the configuration of FIG.
  • size of the member in FIG. 3 is notional, The relative relationship of the magnitude
  • the liquid crystal display device 30 shown in FIG. 3 includes a backlight unit 20 and a liquid crystal cell unit 31 disposed to face the backlight unit 20.
  • the liquid crystal cell unit 31 is configured such that the liquid crystal cell 32 is disposed between the polarizing plate 33A and the polarizing plate 33B.
  • the driving method of the liquid crystal cell 32 is not particularly limited, and is a TN (Twisted Nematic) method, a STN (Super Twisted Nematic) method, a VA (Virtual Alignment) method, an IPS (In-Plane-Switching) method, and an OCB (Optically Filled). The method etc. are mentioned.
  • the curable composition of the present disclosure includes a quantum dot phosphor, an alkyleneoxy group-containing compound having an alkyleneoxy group and a polymerizable reactive group (also simply referred to as “alkyleneoxy group-containing compound” in this disclosure), and photopolymerization initiation. Contains agents.
  • the curable composition of this indication is excellent in the moist heat resistance of hardened
  • the curable composition includes a quantum dot phosphor.
  • the quantum dot phosphor is not particularly limited, and examples thereof include particles containing at least one selected from the group consisting of II-VI group compounds, III-V group compounds, IV-VI group compounds, and IV group compounds. From the viewpoint of luminous efficiency, the quantum dot phosphor preferably contains a compound containing at least one of Cd and In.
  • II-VI group compounds include CdSe, CdTe, CdS, ZnS, ZnSe, ZnTe, ZnO, HgS, HgSe, HgTe, CdSeS, CdSeTe, CdSTe, ZnSeS, ZnSeTe, ZnSTe, HgSeS, HgSeS, HgSeT, CdZnSe, CdZnTe, CdHgS, CdHgSe, CdHgTe, HgZnS, HgZnSe, HgZnTe, CdZnSeS, CdZnSeTe, CdZnSTe, CdHgSeS, CdHgSeTe, GdHgSe, ST Specific examples of the III-V group compounds include GaN, GaP, GaAs, GaSb, AlN, AlP, AlAs, AlSb, InN, In
  • IV-VI group compounds include SnS, SnSe, SnTe, PbS, PbSe, PbTe, SnSeS, SnSeTe, SnSTe, PbSeS, PbSeTe, PbSTe, SnPbS, SnPbSe, SnPbTe, Sn, etc. .
  • group IV compound include Si
  • Quantum dot phosphors preferably have a core-shell structure.
  • the quantum efficiency of the quantum dot phosphor can be further improved.
  • core / shell examples include CdSe / ZnS, InP / ZnS, PbSe / PbS, CdSe / CdS, CdTe / CdS, CdTe / ZnS, and the like.
  • the quantum dot phosphor may have a so-called core multishell structure in which the shell has a multilayer structure.
  • the quantum efficiency of the quantum dot phosphor can be further improved. Is possible.
  • the curable composition may contain one kind of quantum dot phosphor alone, or may contain two or more kinds of quantum dot phosphors in combination.
  • an aspect including a combination of two or more types of quantum dot phosphors for example, an aspect including two or more types of quantum dot phosphors having the same average particle diameter, although the components are different, and a quantum having the same components having different average particle diameters
  • the aspect containing 2 or more types of dot fluorescent substance and the aspect containing 2 or more types of quantum dot fluorescent substance from which a component and an average particle diameter differ are mentioned.
  • the curable composition comprises a quantum dot phosphor G having an emission center wavelength in the green wavelength region of 520 nm to 560 nm and a quantum dot phosphor R having an emission center wavelength in the red wavelength region of 600 nm to 680 nm. May be included.
  • the quantum dot phosphor G and the quantum dot phosphor R Respectively emit green light and red light.
  • white light can be obtained by the green light and red light emitted from the quantum dot phosphor G and the quantum dot phosphor R and the blue light transmitted through the cured product.
  • the quantum dot phosphor may be used in the state of a quantum dot phosphor dispersion liquid dispersed in a dispersion medium.
  • the dispersion medium for dispersing the quantum dot phosphor include water, various organic solvents, and a monofunctional (meth) acrylate compound.
  • the organic solvent that can be used as the dispersion medium include acetone, ethyl acetate, toluene, n-hexane, and the like.
  • the monofunctional (meth) acrylate compound that can be used as the dispersion medium is not particularly limited as long as it is liquid at room temperature (25 ° C.), and examples thereof include isobornyl (meth) acrylate and dicyclopentanyl (meth) acrylate. Can be mentioned.
  • the dispersion medium is preferably a monofunctional (meth) acrylate compound and has an alicyclic structure from the viewpoint that the step of volatilizing the dispersion medium when curing the curable composition is unnecessary.
  • a monofunctional (meth) acrylate compound is more preferable, isobornyl (meth) acrylate and dicyclopentanyl (meth) acrylate are more preferable, and isobornyl (meth) acrylate is particularly preferable.
  • the mass-based content ratio of the monofunctional (meth) acrylate compound and the alkyleneoxy group-containing compound is 0.01 to 0.30 is preferable, 0.02 to 0.20 is more preferable, and 0.05 to 0.20 is still more preferable.
  • the proportion of the quantum dot phosphor based on the mass of the quantum dot phosphor dispersion is preferably 1% by mass to 10% by mass, more preferably 1% by mass to 5% by mass, and more preferably 2% by mass to More preferably, it is 4.9% by mass.
  • the content of the quantum dot phosphor dispersion in the curable composition is such that the proportion of the quantum dot phosphor based on the mass of the quantum dot phosphor dispersion is 1% by mass to 10% by mass. For example, it is preferably 0.5% by mass to 8% by mass, more preferably 0.8% by mass to 5% by mass, and 1.0% by mass to 4.9% by mass with respect to the total amount of More preferably. Further, the content of the quantum dot phosphor in the curable composition is preferably, for example, 0.05% by mass to 0.8% by mass with respect to the total amount of the curable composition, and 0.08% by mass % To 0.5% by mass is more preferable, and 0.1% to 0.49% by mass is even more preferable.
  • the content of the quantum dot phosphor is 0.05% by mass or more, a sufficient emission intensity tends to be obtained when the cured product is irradiated with excitation light, and the content of the quantum dot phosphor is 0.8.
  • the content is less than or equal to mass%, aggregation of the quantum dot phosphor tends to be suppressed.
  • the curable composition of the present disclosure includes an alkyleneoxy group-containing compound having an alkyleneoxy group and a polymerizable reactive group.
  • the alkyleneoxy group-containing compound preferably has two or more polymerizable reactive groups, and more preferably has two polymerizable reactive groups.
  • the polymerizable reactive group include a functional group having an ethylenic double bond, and more specifically, a (meth) acryloyl group.
  • alkyleneoxy group for example, an alkyleneoxy group having 2 to 4 carbon atoms is preferable, an alkyleneoxy group having 2 or 3 carbon atoms is more preferable, and an alkyleneoxy group having 2 carbon atoms is more preferable.
  • the alkyleneoxy group-containing compound may have one type of alkyleneoxy group or may have two or more types of alkyleneoxy groups.
  • the alkyleneoxy group-containing compound may be a polyalkyleneoxy group-containing compound having a polyalkyleneoxy group containing a plurality of alkyleneoxy groups.
  • the alkyleneoxy group-containing compound preferably has 2 to 30 alkyleneoxy groups, more preferably 2 to 20 alkyleneoxy groups, and more preferably 3 to 10 alkyleneoxy groups. Is more preferable, and it is particularly preferable to have 3 to 5 alkyleneoxy groups.
  • the alkyleneoxy group-containing compound preferably has a bisphenol structure. Thereby, it exists in the tendency which is more excellent in heat-and-moisture resistance.
  • the bisphenol structure include a bisphenol A structure and a bisphenol F structure, and among them, the bisphenol A structure is preferable.
  • alkyleneoxy group-containing compound examples include alkoxyalkyl (meth) acrylates such as butoxyethyl (meth) acrylate; diethylene glycol monoethyl ether (meth) acrylate, triethylene glycol monobutyl ether (meth) acrylate, tetraethylene glycol monomethyl ether (Meth) acrylate, hexaethylene glycol monomethyl ether (meth) acrylate, octaethylene glycol monomethyl ether (meth) acrylate, nonaethylene glycol monomethyl ether (meth) acrylate, dipropylene glycol monomethyl ether (meth) acrylate, heptapropylene glycol monomethyl ether (Meth) acrylate, tetraethylene glycol monoethyl acetate
  • Poly (alkylene glycol) monoalkyl ether (meth) acrylates such as ru (meth) acrylate; Polyalkylene glycol monoaryl ether (me
  • alkyleneoxy group-containing compounds ethoxylated bisphenol A di (meth) acrylate, propoxylated bisphenol A di (meth) acrylate and propoxylated ethoxylated bisphenol A di (meth) acrylate are preferred, and ethoxylated bisphenol A di ( More preferred is (meth) acrylate.
  • the alkyleneoxy group-containing compound one type may be used alone, or two or more types may be used in combination.
  • the content of the alkyleneoxy group-containing compound in the curable composition is preferably, for example, 30% by mass to 70% by mass, and preferably 35% by mass to 65% by mass with respect to the total amount of the curable composition. It is preferably 40% by mass to 60% by mass.
  • the content of the alkyleneoxy group-containing compound is 30% by mass or more, moisture permeability tends to be suppressed from being excessively high.
  • the content of the alkyleneoxy group-containing compound is 70% by mass or less, curability is obtained. There exists a tendency which can suppress the fall of the water vapor transmission rate of a composition.
  • the curable composition of the present disclosure preferably includes a polyfunctional thiol compound.
  • the curable composition contains a polyfunctional thiol compound
  • the enethiol reaction proceeds between the alkyleneoxy group-containing compound and the polyfunctional thiol compound when the curable composition is cured, and the heat resistance of the cured product is increased. It tends to improve.
  • polyfunctional thiol compound examples include ethylene glycol bis (3-mercaptopropionate), diethylene glycol bis (3-mercaptopropionate), tetraethylene glycol bis (3-mercaptopropionate), 1,2- Propylene glycol bis (3-mercaptopropionate), diethylene glycol bis (3-mercaptobutyrate), 1,4-butanediol bis (3-mercaptopropionate), 1,4-butanediol bis (3-mercaptobutyrate) Rate), 1,8-octanediol bis (3-mercaptopropionate), 1,8-octanediol bis (3-mercaptobutyrate), hexanediol bisthioglycolate, trimethylolpropane tris (3-mercaptopropiate) Onee ), Trimethylolpropane tris (3-mercaptobutyrate), trimethylolpropane tris (3-mercaptoisobutyrate), trimethylol
  • the curable composition of the present disclosure may contain a monofunctional thiol compound having one thiol group in one molecule.
  • monofunctional thiol compounds include hexanethiol, 1-heptanethiol, 1-octanethiol, 1-nonanethiol, 1-decanethiol, 3-mercaptopropionic acid, methyl mercaptopropionate, methoxybutyl mercaptopropionate, Examples include octyl mercaptopropionate, tridecyl mercaptopropionate, 2-ethylhexyl-3-mercaptopropionate, n-octyl-3-mercaptopropionate, and the like.
  • the content of the thiol compound in the curable composition is:
  • the content is preferably 15% by mass to 70% by mass, more preferably 20% by mass to 65% by mass, and more preferably 25% by mass to 60% by mass with respect to the total amount of the curable composition. More preferably, the content is 30% by mass to 50% by mass. It exists in the tendency which can suppress the fall of the water vapor transmission rate of a curable composition because the content rate of a thiol compound is 15 mass% or more.
  • the content of the thiol compound is 70% by mass or less, the moisture permeability tends to be suppressed from becoming too high.
  • the proportion of the polyfunctional thiol compound based on the mass of the polyfunctional thiol compound and the monofunctional thiol compound used as necessary is preferably 60% by mass to 100% by mass, and more preferably 70% by mass to 100% by mass. More preferably, it is more preferably 80% by mass to 100% by mass.
  • Ratio of the number of thiol groups in the thiol compound (the sum of the polyfunctional thiol compound and the monofunctional thiol compound used as necessary, preferably the polyfunctional thiol compound) to the number of polymerizable reactive groups in the alkyleneoxy group-containing compound (Number of thiol groups / number of polymerizable reactive groups) is preferably 0.5 to 5.0, more preferably 0.8 to 4.0, and 1.0 to 3.5. More preferably, it is particularly preferably 1.2 to 3.0.
  • the curable composition of the present disclosure includes a photopolymerization initiator.
  • the photopolymerization initiator is not particularly limited, and specific examples include compounds that generate radicals upon irradiation with active energy rays such as ultraviolet rays.
  • the photopolymerization initiator include benzophenone, N, N′-tetraalkyl-4,4′-diaminobenzophenone, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1, 2-methyl-1- [4- (methylthio) phenyl] -2-morpholino-propanone-1,4,4′-bis (dimethylamino) benzophenone (also referred to as “Michler ketone”), 4,4′-bis (Diethylamino) benzophenone, 4-methoxy-4′-dimethylaminobenzophenone, 1-hydroxycyclohexyl phenyl ketone, 1- (4-isopropylphenyl) -2-hydroxy-2-methylpropan-1-one, 1- (4- (2-hydroxyethoxy) -phenyl) -2-hydroxy-2-methyl-1-propane-1 Aromatic ketone compounds such as ON and 2-hydroxy-2-methyl
  • the photopolymerization initiator is preferably at least one selected from the group consisting of an acylphosphine oxide compound, an aromatic ketone compound, and an oxime ester compound from the viewpoint of curability, and includes an acylphosphine oxide compound and an aromatic ketone compound. More preferably, at least one selected from the group consisting of acylphosphine oxide compounds is more preferable.
  • the content of the photopolymerization initiator in the curable composition is preferably, for example, 0.1% by mass to 5% by mass, and preferably 0.1% by mass to 3% by mass with respect to the total amount of the curable composition. %, More preferably 0.3% by mass to 1.5% by mass.
  • the content of the photopolymerization initiator is 0.1% by mass or more, the sensitivity of the curable composition tends to be sufficient, and when the content of the photopolymerization initiator is 5% by mass or less, There exists a tendency for the influence on the hue of a curable composition and the fall of storage stability to be suppressed.
  • the curable composition of the present disclosure may include a liquid medium.
  • a liquid medium means a medium in a liquid state at room temperature (25 ° C.).
  • liquid medium examples include acetone, methyl ethyl ketone, methyl-n-propyl ketone, methyl isopropyl ketone, methyl-n-butyl ketone, methyl isobutyl ketone, methyl-n-pentyl ketone, methyl-n-hexyl ketone, diethyl ketone, Ketone solvents such as dipropyl ketone, diisobutyl ketone, trimethylnonanone, cyclohexanone, cyclopentanone, methylcyclohexanone, 2,4-pentanedione, acetonylacetone; diethyl ether, methyl ethyl ether, methyl-n-propyl ether, diisopropyl Ether, tetrahydrofuran, methyltetrahydrofuran, dioxane, dimethyldioxane, ethylene glycol dimethyl ether
  • Glycol monoether solvents such as Terpene solvents such as terpinene, terpineol, myrcene, alloocimene, limonene, dipentene, pinene, carvone, oximene, and ferrandylene; straight silicone oils such as dimethyl silicone oil, methylphenyl silicone oil, and methylhydrogen silicone oil Amino-modified silicone oil, epoxy-modified silicone oil, cal Xyoxy-modified silicone oil, carbinol-modified silicone oil, mercapto-modified silicone oil, heterogeneous functional group-modified silicone oil, polyether-modified silicone oil, methylstyryl-modified silicone oil, hydrophilic specially-modified silicone oil, higher alkoxy-modified silicone oil, higher fatty acid Modified silicone oil such as modified silicone oil and fluorine-modified silicone oil; butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, oct
  • the content of the liquid medium in the curable composition is preferably, for example, 1% by mass to 10% by mass with respect to the total amount of the curable composition.
  • the content is more preferably 10% by mass to 10% by mass, and further preferably 4% by mass to 7% by mass.
  • the curable composition of the present disclosure may contain a carboxylic acid having 1 to 17 carbon atoms (hereinafter also referred to as “specific carboxylic acid”).
  • the specific carboxylic acid is a carboxylic acid having 2 to 12 carbon atoms from the viewpoint of being hard to be stained on the surface of the cured product, excellent in reliability of the cured product, and having less steric hindrance and being easily coordinated to the quantum dot phosphor.
  • the carboxylic acid having 2 to 10 carbon atoms is more preferable, the carboxylic acid having 3 to 8 carbon atoms is more preferable, the carboxylic acid having 3 to 6 carbon atoms is particularly preferable, and the carboxylic acid having 3 to 5 carbon atoms is more preferable. Acid is even more preferred.
  • carbon of a carboxy group shall be included in the carbon number in specific carboxylic acid.
  • the specific carboxylic acid may be an unsaturated carboxylic acid or a saturated carboxylic acid.
  • the carbon-carbon double bond in the unsaturated carboxylic acid reacts with the thiol group in the polyfunctional thiol compound, so that the specific carboxylic acid is less likely to be stained on the surface of the cured product, and from the viewpoint of excellent reliability of the cured product.
  • Unsaturated carboxylic acid is preferable, and methacrylic acid, acrylic acid and the like are more preferable.
  • the specific carboxylic acid may be a carboxylic acid having one or more carboxy groups, or a carboxylic acid having two or more carboxy groups.
  • the specific carboxylic acid may have a substituent.
  • substituents include a thiol group, amino group, hydroxy group, alkoxy group, acyl group, sulfonic acid group, aryl group, halogen atom, methacryl group and acrylic group.
  • the number of carbon atoms in the specific carboxylic acid does not include carbon in the substituent.
  • carboxylic acid examples include formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, caproic acid, 2-ethylbutyric acid, enanthic acid, caprylic acid, pelargonic acid, capric acid, Lauric acid, mytilic acid, palmitic acid, margaric acid, methacrylic acid, acrylic acid, fumaric acid, maleic acid, mercaptoacetic acid, mercaptopropionic acid, mercaptobutyric acid, mercaptovaleric acid, lactic acid, malic acid, citric acid, benzoic acid, phenyl Examples include acetic acid, phenylpropionic acid, phthalic acid, isophthalic acid, terephthalic acid, salicylic acid, and ⁇ -aminocaproic acid.
  • the specific carboxylic acid preferably includes at least one selected from the group consisting of acetic acid, mercaptopropionic acid, and methacrylic acid.
  • the specific carboxylic acid one type may be used alone, or two or more types may be used in combination.
  • the content ratio (specific carboxylic acid / quantum dot phosphor) of the specific carboxylic acid with respect to the quantum dot phosphor on the mass basis determines the reliability of the cured product and the quantum dot fluorescence. From the viewpoint of coordination to the body, it is preferably 0.06 to 6.2, more preferably 0.08 to 5.5, and still more preferably 0.09 to 5.3. .
  • the curable composition of the present disclosure may or may not contain a carboxylic acid having 18 or more carbon atoms such as oleic acid.
  • the curable composition of the present disclosure may contain a white pigment.
  • the white pigment include titanium oxide, barium sulfate, zinc oxide, calcium carbonate and the like. Among these, titanium oxide is preferable from the viewpoint of light scattering efficiency.
  • the curable composition contains titanium oxide as a white pigment, the titanium oxide may be rutile titanium oxide or anatase titanium oxide, and is preferably rutile titanium oxide.
  • the average particle diameter of the white pigment is preferably 0.1 ⁇ m to 1 ⁇ m, more preferably 0.2 ⁇ m to 0.8 ⁇ m, and further preferably 0.2 ⁇ m to 0.5 ⁇ m.
  • the average particle size of the white pigment can be measured as follows.
  • the white pigment extracted from the curable composition is dispersed in purified water containing a surfactant to obtain a dispersion.
  • a laser diffraction particle size distribution measuring apparatus for example, Shimadzu Corporation, SALD-3000J
  • the median diameter (D50) is defined as the average particle diameter of the white pigment.
  • the curable composition can be obtained by diluting the curable composition with a liquid medium, precipitating the white pigment by a centrifugal treatment or the like, and collecting the white pigment.
  • the average particle diameter of the white pigment contained in the cured product is calculated by calculating the equivalent circle diameter (the geometric average of the major axis and the minor axis) for 50 particles by observing the particles using a scanning electron microscope. It can be obtained as an arithmetic average value.
  • the white particles preferably have an organic layer containing an organic substance on at least a part of the surface from the viewpoint of suppressing aggregation of the white pigment in the curable composition.
  • Organic substances contained in the organic layer include organic silane, organosiloxane, fluorosilane, organic phosphonate, organic phosphoric acid compound, organic phosphinate, organic sulfonic acid compound, carboxylic acid, carboxylic acid ester, carboxylic acid derivative, amide, hydrocarbon Examples thereof include waxes, polyolefins, polyolefin copolymers, polyols, polyol derivatives, alkanolamines, alkanolamine derivatives, and organic dispersants.
  • the organic material contained in the organic material layer preferably contains a polyol, an organic silane, or the like, and more preferably contains at least one of a polyol or an organic silane.
  • the organic silane include octyltriethoxysilane, nonyltriethoxysilane, decyltriethoxysilane, dodecyltriethoxysilane, tridecyltriethoxysilane, tetradecyltriethoxysilane, pentadecyltriethoxysilane, hexadecyltriethoxy Silane, heptadecyltriethoxysilane, octadecyltriethoxysilane, etc.
  • organosiloxanes include polydimethylsiloxane terminated with a trimethylsilyl functional group (PDMS), polymethylhydrosiloxane (PMHS), polysiloxane derived by functionalization of PMHS with an olefin (by hydrosilylation), and the like. It is done.
  • organic phosphonate include, for example, n-octyl phosphonic acid and its ester, n-decyl phosphonic acid and its ester, 2-ethylhexyl phosphonic acid and its ester, and camphyl phosphonic acid and its ester.
  • organic phosphate compound examples include organic acidic phosphates, organic pyrophosphates, organic polyphosphates, organic metaphosphates, salts thereof, and the like.
  • organic phosphinate examples include n-hexylphosphinic acid and its ester, n-octylphosphinic acid and its ester, di-n-hexylphosphinic acid and its ester, and di-n-octylphosphinic acid and its ester. Can be mentioned.
  • organic sulfonic acid compound examples include hexyl sulfonic acid, octyl sulfonic acid, alkyl sulfonic acid such as 2-ethylhexyl sulfonic acid, these alkyl sulfonic acids and metal ions such as sodium, calcium, magnesium, aluminum and titanium, ammonium And salts with organic ammonium ions such as ions and triethanolamine.
  • carboxylic acid include maleic acid, malonic acid, fumaric acid, benzoic acid, phthalic acid, stearic acid, oleic acid, linoleic acid and the like.
  • carboxylic acid ester examples include the above carboxylic acid and ethylene glycol, propylene glycol, trimethylolpropane, diethanolamine, triethanolamine, glycerol, hexanetriol, erythritol, mannitol, sorbitol, pentaerythritol, bisphenol A, hydroquinone, furoquinone, Examples thereof include esters and partial esters formed by reaction with hydroxy compounds such as loglucinol.
  • Specific examples of the amide include stearic acid amide, oleic acid amide, erucic acid amide and the like.
  • polyolefin and its copolymer examples include a copolymer of polyethylene, polypropylene, ethylene and one or more compounds selected from propylene, butylene, vinyl acetate, acrylate, acrylamide, and the like.
  • polyol examples include glycerol, trimethylol ethane, trimethylol propane and the like.
  • alkanolamine examples include diethanolamine and triethanolamine.
  • organic dispersants include citric acid, polyacrylic acid, polymethacrylic acid, high molecular organic dispersants having functional groups such as anionic, cationic, zwitterionic, and nonionic.
  • the white pigment may have a metal oxide layer containing a metal oxide on at least a part of the surface.
  • the metal oxide contained in the metal oxide layer include silicon dioxide, aluminum oxide, zirconia, phosphoria, and boria.
  • the metal oxide layer may be a single layer or two or more layers.
  • the white pigment preferably includes a first metal oxide layer containing silicon dioxide and a second metal oxide layer containing aluminum oxide.
  • the white pigment has a metal oxide layer, the dispersibility of the white pigment in a cured product containing an alicyclic structure and a sulfide structure tends to be improved.
  • the white pigment may have an organic layer and a metal oxide layer.
  • the metal oxide layer and the organic material layer are provided in the order of the metal oxide layer and the organic material layer on the surface of the white pigment.
  • the surface of the white pigment has a first metal oxide layer containing silicon dioxide, a second metal oxide layer containing aluminum oxide, and an organic material. It is preferable that a layer is provided in order of a 1st metal oxide layer, a 2nd metal oxide layer, and an organic substance layer.
  • the content of the white pigment in the curable composition is, for example, 0.05% by mass to 1.0% by mass with respect to the total amount of the curable composition. It is preferably 0.1% by mass to 1.0% by mass, and more preferably 0.2% by mass to 0.5% by mass.
  • the curable composition may further contain other components such as a polymerization inhibitor, a silane coupling agent, a surfactant, an adhesion imparting agent, and an antioxidant.
  • the curable composition may contain one kind of each of other components, or may contain two or more kinds in combination.
  • the curable composition may contain the (meth) allyl compound as needed.
  • the curable composition may be prepared by, for example, a quantum dot phosphor, an alkyleneoxy group-containing compound having an alkyleneoxy group and a polymerizable reactive group, a polyfunctional thiol compound, a photopolymerization initiator, and, if necessary, the above-described components according to a conventional method. It can be prepared by mixing.
  • the quantum dot phosphor is preferably mixed while being dispersed in a dispersion medium.
  • the curable composition can be suitably used for film formation. Moreover, a curable composition can be used conveniently for formation of a wavelength conversion member.
  • Examples 1 to 4 and Comparative Examples 1 and 2 (Preparation of curable composition)
  • the curable compositions of Examples 1 to 5 and Comparative Examples 1 and 2 were prepared by mixing the components shown in Table 1 in the blending amounts (unit: parts by mass) shown in the same table. "-" In Table 1 means not blended.
  • Tricyclodecane dimethanol diacrylate (Shin Nakamura Chemical Co., Ltd., A-DCP) was used as the polyfunctional (meth) acrylate compound (comparative compound) having an alicyclic structure, and as an alkyleneoxy group-containing compound. Used ethoxylated bisphenol A diacrylate (Shin Nakamura Chemical Co., Ltd., ABE-300).
  • pentaerythritol tetrakis (3-mercaptopropionate) (SC Organic Chemical Co., PEMP) was used as the polyfunctional thiol compound.
  • PEMP pentaerythritol tetrakis (3-mercaptopropionate)
  • BASF 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide
  • a CdSe / ZnS (core / shell) dispersion Nanosys, Gen 3.5 QD Concentrate
  • Isobornyl acrylate was used as a dispersion medium for this CdSe / ZnS (core / shell) dispersion. 90% by mass or more of isobornyl acrylate is contained in the CdSe / ZnS (core / shell) dispersion. Acetic acid was used as the carboxylic acid.
  • titanium oxide (Chemours, Taipure R-706, particle size 0.36 ⁇ m) was used as a white pigment. On the surface of titanium oxide, a first metal oxide layer containing silicon oxide, a second metal oxide layer containing aluminum oxide, and an organic material layer containing a polyol compound are formed into a first metal oxide layer and a second metal oxide layer. And an organic material layer.
  • Each wavelength conversion member obtained above was cut into a 17 mm diameter to prepare a sample for evaluation.
  • the initial emission intensity of the sample for evaluation was measured with a fiber multichannel spectrometer (Ocean Photonics Co., Ltd., Ocean View).
  • the sample for evaluation was put into a constant temperature and humidity chamber under an environment of 85 ° C. and 95% RH (relative humidity) and allowed to stand for 1000 hours, and then the emission intensity was measured.
  • the relative light emission intensity retention rate of the wavelength conversion member was calculated according to the following formula. Relative emission intensity retention rate: (RLb / RLa) ⁇ 100 RLa:
  • Initial relative light emission intensity RLb Relative light emission intensity after 1000 hours in an environment of 85 ° C. and 95% RH Note that the higher the value of the relative light emission intensity retention rate, the better the wavelength conversion member is in heat and moisture resistance.
  • the storage elastic modulus (E ′) and loss elastic modulus (E ′′) of the cured product for evaluation were measured under the condition of “temperature rate: 10 ° C./min”, and the loss tangent (tan ⁇ ) was obtained from the ratio, and the loss tangent
  • the glass transition temperature (Tg) was determined from the temperature at the peak top portion of (tan ⁇ ).
  • V2 Peak area of a peak attributed to SH stretching vibration (peak wavelength: 2570 cm ⁇ 1 )

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Abstract

A wavelength conversion member which is provided with a cured product that contains a quantum dot phosphor, while having an alkyleneoxy structure.

Description

波長変換部材、バックライトユニット、画像表示装置及び硬化性組成物Wavelength conversion member, backlight unit, image display device, and curable composition
　本発明は、波長変換部材、バックライトユニット、画像表示装置及び硬化性組成物に関する。 The present invention relates to a wavelength conversion member, a backlight unit, an image display device, and a curable composition.
　近年、液晶表示装置等の画像表示装置の分野においては、ディスプレイの色再現性を向上させることが求められている。色再現性を向上させる手段として、特表２０１３－５４４０１８号公報及び国際公開第２０１６／０５２６２５号に記載のように、量子ドット蛍光体を含む波長変換部材が注目を集めている。 In recent years, in the field of image display devices such as liquid crystal display devices, it has been required to improve the color reproducibility of displays. As means for improving color reproducibility, wavelength conversion members including quantum dot phosphors are attracting attention as described in JP 2013-544018 A and International Publication No. 2016/052625.
　量子ドット蛍光体を含む波長変換部材は、例えば、画像表示装置のバックライトユニットに配置される。赤色光を発光する量子ドット蛍光体及び緑色光を発光する量子ドット蛍光体を含む波長変換部材を用いる場合、波長変換部材に対して励起光としての青色光を照射すると、量子ドット蛍光体から発光された赤色光及び緑色光と、波長変換部材を透過した青色光とにより、白色光を得ることができる。量子ドット蛍光体を含む波長変換部材の開発により、ディスプレイの色再現性は、従来のＮＴＳＣ（Ｎａｔｉｏｎａｌ　Ｔｅｌｅｖｉｓｉｏｎ　Ｓｙｓｔｅｍ　Ｃｏｍｍｉｔｔｅｅ）比７２％からＮＴＳＣ比１００％へと拡大している。 The wavelength conversion member including the quantum dot phosphor is disposed, for example, in the backlight unit of the image display device. When a wavelength conversion member including a quantum dot phosphor that emits red light and a quantum dot phosphor that emits green light is used, when the wavelength conversion member is irradiated with blue light as excitation light, the quantum dot phosphor emits light. White light can be obtained by the red light and green light that have been generated and the blue light that has passed through the wavelength conversion member. With the development of wavelength conversion members including quantum dot phosphors, the color reproducibility of displays has been expanded from 72% of the conventional NTSC (National Television System Committee) ratio to 100% of the NTSC ratio.
　量子ドット蛍光体を含む波長変換部材は、通常、量子ドット蛍光体を含む硬化性組成物を硬化させた硬化物を有する。硬化性組成物としては熱硬化型及び光硬化型があり、生産性の観点からは光硬化型の硬化性組成物が好ましく用いられる。 The wavelength conversion member containing the quantum dot phosphor usually has a cured product obtained by curing a curable composition containing the quantum dot phosphor. The curable composition includes a thermosetting type and a photocurable type, and a photocurable type curable composition is preferably used from the viewpoint of productivity.
　ところで、量子ドット蛍光体を含む波長変換部材では、量子ドット蛍光体を含む硬化物の少なくとも一部が被覆材によって被覆される場合がある。例えば、フィルム状の波長変換材の場合、量子ドット蛍光体を含む硬化物の片面又は両面に、酸素に対するバリア性を有するバリアフィルムが設けられることがある。 By the way, in the wavelength conversion member containing quantum dot fluorescent substance, at least one part of the hardened | cured material containing quantum dot fluorescent substance may be coat | covered with a coating material. For example, in the case of a film-like wavelength conversion material, a barrier film having a barrier property against oxygen may be provided on one side or both sides of a cured product containing a quantum dot phosphor.
　このように酸素に対するバリア性を有するバリアフィルムを設けた場合であっても、硬化物中の量子ドット蛍光体は酸素の影響により劣化するという問題が生じやすい。そのため、量子ドット蛍光体を含む波長変換部材を高温高湿環境下で放置した場合に、量子ドット蛍光体が劣化し発光強度が低下するおそれがある。 Even when a barrier film having a barrier property against oxygen is provided in this way, the quantum dot phosphor in the cured product is likely to deteriorate due to the influence of oxygen. Therefore, when the wavelength conversion member containing the quantum dot phosphor is left in a high-temperature and high-humidity environment, the quantum dot phosphor may deteriorate and the emission intensity may decrease.
　特に、量子ドット蛍光体を含む光硬化型の硬化性組成物の硬化物は、高温高湿環境下での耐久性（耐湿熱性）が不十分であり、量子ドット蛍光体が劣化し発光強度が低下しやすい傾向にある。 In particular, a cured product of a photocurable curable composition containing a quantum dot phosphor has insufficient durability (moisture and heat resistance) in a high-temperature and high-humidity environment, and the quantum dot phosphor is deteriorated and has a light emission intensity. It tends to decrease.
　本開示は、上記事情に鑑みてなされたものであり、量子ドット蛍光体を含み、耐湿熱性に優れる波長変換部材並びにこれを用いたバックライトユニット及び画像表示装置を提供することを目的とする。さらに、本開示は、量子ドット蛍光体を含み、耐湿熱性に優れる硬化物を形成可能な硬化性組成物を提供することを目的とする。 The present disclosure has been made in view of the above circumstances, and an object of the present disclosure is to provide a wavelength conversion member that includes a quantum dot phosphor and is excellent in moisture and heat resistance, a backlight unit using the same, and an image display device. Furthermore, this indication aims at providing the curable composition which can form the hardened | cured material which is excellent in wet heat resistance including quantum dot fluorescent substance.
　前記課題を達成するための具体的手段は以下の通りである。
＜１＞　量子ドット蛍光体を含み、アルキレンオキシ構造を有する硬化物を備える、波長変換部材。
＜２＞　前記硬化物は、スルフィド構造を有する、＜１＞に記載の波長変換部材。
＜３＞　前記量子ドット蛍光体がＣｄ及びＩｎの少なくとも一方を含む化合物を含む、＜１＞又は＜２＞に記載の波長変換部材。
＜４＞　前記硬化物の少なくとも一部を被覆する被覆材をさらに有する、＜１＞～＜３＞のいずれか１つに記載の波長変換部材。
＜５＞　前記硬化物におけるジヨードメタンの接触角及び水の接触角を用い、Ｗｕの式より算出される極性成分は、５ｍＪ／ｍ２～１２ｍＪ／ｍ２である、＜１＞～＜４＞のいずれか１つに記載の波長変換部材。
＜６＞　フーリエ変換赤外分光光度計で測定した前記硬化物における、Ｃ＝Ｃ伸縮振動に帰属されるピーク面積（Ｖ１）と、Ｓ－Ｈ伸縮振動に帰属されるピーク面積（Ｖ２）との比率（Ｖ１／Ｖ２）が、０．０００５２以下である、＜１＞～＜５＞のいずれか１つに記載の波長変換部材。
＜７＞　動的粘弾性測定により測定された前記硬化物のガラス転移温度が、４７℃以下である＜１＞～＜６＞のいずれか１つに記載の波長変換部材。 Specific means for achieving the above object are as follows.
<1> A wavelength conversion member comprising a cured product including a quantum dot phosphor and having an alkyleneoxy structure.
<2> The wavelength conversion member according to <1>, wherein the cured product has a sulfide structure.
<3> The wavelength conversion member according to <1> or <2>, wherein the quantum dot phosphor includes a compound containing at least one of Cd and In.
<4> The wavelength conversion member according to any one of <1> to <3>, further including a covering material that covers at least a part of the cured product.
<5> The polar component calculated from the formula of Wu using the contact angle of diiodomethane and the contact angle of water in the cured product is 5 mJ / m 2 to 12 mJ / m 2 , from <1> to <4> The wavelength conversion member as described in any one.
<6> A peak area (V1) attributed to C = C stretching vibration and a peak area (V2) attributed to SH stretching vibration in the cured product measured with a Fourier transform infrared spectrophotometer. The wavelength conversion member according to any one of <1> to <5>, wherein the ratio (V1 / V2) is 0.00052 or less.
<7> The wavelength conversion member according to any one of <1> to <6>, wherein a glass transition temperature of the cured product measured by dynamic viscoelasticity measurement is 47 ° C. or lower.
＜８＞　＜１＞～＜７＞のいずれか１つに記載の波長変換部材と、光源とを備えるバックライトユニット。 <8> A backlight unit comprising the wavelength conversion member according to any one of <1> to <7> and a light source.
＜９＞　＜８＞に記載のバックライトユニットを備える画像表示装置。 <9> An image display device comprising the backlight unit according to <8>.
＜１０＞　量子ドット蛍光体、アルキレンオキシ基及び重合性反応基を有するアルキレンオキシ基含有化合物並びに光重合開始剤を含む、硬化性組成物。
＜１１＞　多官能チオール化合物をさらに含む、＜１０＞に記載の硬化性組成物。
＜１２＞　前記多官能チオール化合物の含有率は、前記硬化性組成物の全量に対して１５質量％～７０質量％である、＜１１＞に記載の硬化性組成物。
＜１３＞　前記アルキレンオキシ基含有化合物中の重合性反応基の数に対する前記多官能チオール化合物中のチオール基の数の比率（チオール基の数／重合性反応基の数）は、０．５～５．０である、＜１１＞又は＜１２＞に記載の硬化性組成物。
＜１４＞　前記アルキレンオキシ基含有化合物の含有率は、前記硬化性組成物の全量に対して３０質量％～７０質量％である、＜１０＞～＜１３＞のいずれか１つに記載の硬化性組成物。
＜１５＞　前記重合性反応基は、（メタ）アクリロイル基を含む、＜１０＞～＜１４＞のいずれか１つに記載の硬化性組成物。
＜１６＞　炭素数１～１７であるカルボン酸をさらに含む、＜１０＞～＜１５＞のいずれか１つに記載の硬化性組成物。
＜１７＞　白色顔料をさらに含む、＜１０＞～＜１６＞のいずれか１つに記載の硬化性組成物。 <10> A curable composition comprising a quantum dot phosphor, an alkyleneoxy group-containing compound having an alkyleneoxy group and a polymerizable reactive group, and a photopolymerization initiator.
<11> The curable composition according to <10>, further comprising a polyfunctional thiol compound.
<12> The curable composition according to <11>, wherein the content of the polyfunctional thiol compound is 15% by mass to 70% by mass with respect to the total amount of the curable composition.
<13> The ratio of the number of thiol groups in the polyfunctional thiol compound to the number of polymerizable reactive groups in the alkyleneoxy group-containing compound (the number of thiol groups / the number of polymerizable reactive groups) is 0.5 to The curable composition according to <11> or <12>, which is 5.0.
<14> The curing rate according to any one of <10> to <13>, wherein the content of the alkyleneoxy group-containing compound is 30% by mass to 70% by mass with respect to the total amount of the curable composition. Sex composition.
<15> The curable composition according to any one of <10> to <14>, wherein the polymerizable reactive group includes a (meth) acryloyl group.
<16> The curable composition according to any one of <10> to <15>, further comprising a carboxylic acid having 1 to 17 carbon atoms.
<17> The curable composition according to any one of <10> to <16>, further comprising a white pigment.
　本開示によれば、量子ドット蛍光体を含み、耐湿熱性に優れる波長変換部材並びにこれを用いたバックライトユニット及び画像表示装置を提供することができる。
　さらに、本開示によれば、量子ドット蛍光体を含み、耐湿熱性に優れる硬化物を形成可能な硬化性組成物を提供することができる。 According to the present disclosure, it is possible to provide a wavelength conversion member that includes a quantum dot phosphor and is excellent in moisture and heat resistance, and a backlight unit and an image display device using the wavelength conversion member.
Furthermore, according to the present disclosure, it is possible to provide a curable composition capable of forming a cured product that includes a quantum dot phosphor and is excellent in moisture and heat resistance.
波長変換部材の概略構成の一例を示す模式断面図である。It is a schematic cross section which shows an example of schematic structure of a wavelength conversion member. バックライトユニットの概略構成の一例を示す図である。It is a figure which shows an example of schematic structure of a backlight unit. 液晶表示装置の概略構成の一例を示す図である。It is a figure which shows an example of schematic structure of a liquid crystal display device.
　以下、本発明を実施するための形態について詳細に説明する。但し、本発明は以下の実施形態に限定されるものではない。以下の実施形態において、その構成要素（要素ステップ等も含む）は、特に明示した場合を除き、必須ではない。数値及びその範囲についても同様であり、本発明を制限するものではない。
　本開示において「～」を用いて示された数値範囲には、「～」の前後に記載される数値がそれぞれ最小値及び最大値として含まれる。
　本開示中に段階的に記載されている数値範囲において、一つの数値範囲で記載された上限値又は下限値は、他の段階的な記載の数値範囲の上限値又は下限値に置き換えてもよい。また、本開示中に記載されている数値範囲において、その数値範囲の上限値又は下限値は、実施例に示されている値に置き換えてもよい。
　本開示において各成分は該当する物質を複数種含んでいてもよい。組成物中に各成分に該当する物質が複数種存在する場合、各成分の含有率又は含有量は、特に断らない限り、組成物中に存在する当該複数種の物質の合計の含有率又は含有量を意味する。
　本開示において各成分に該当する粒子は複数種含んでいてもよい。組成物中に各成分に該当する粒子が複数種存在する場合、各成分の粒子径は、特に断らない限り、組成物中に存在する当該複数種の粒子の混合物についての値を意味する。
　本開示において「層」又は「膜」との語には、当該層又は膜が存在する領域を観察したときに、当該領域の全体に形成されている場合に加え、当該領域の一部にのみ形成されている場合も含まれる。
　本開示において「積層」との語は、層を積み重ねることを示し、二以上の層が結合されていてもよく、二以上の層が着脱可能であってもよい。
　本開示において「（メタ）アクリロイル」とは、アクリロイル及びメタクリロイルの少なくとも一方を意味し、「（メタ）アクリレート」はアクリレート及びメタクリレートの少なくとも一方を意味し、「（メタ）アリル」はアリル及びメタリルの少なくとも一方を意味する。
　また、本開示において、チオール基及びアルキレンオキシ基の両方を含む化合物は、チオール化合物に分類するものとする。
　また、本開示において、エステル結合の酸素原子と当該酸素原子と隣り合う炭素原子とが結合した構造（－Ｃ（＝Ｏ）－Ｏ－Ｒにおける－Ｏ－Ｒ、Ｒは置換基を表す）、及び水酸基の酸素原子と当該酸素原子と隣り合う炭素原子とが結合した構造（ＨＯ－ＲにおけるＯ－Ｒ、Ｒは置換基を表す）は、アルキレンオキシ基に分類しないものとする。 Hereinafter, embodiments for carrying out the present invention will be described in detail. However, the present invention is not limited to the following embodiments. In the following embodiments, the components (including element steps and the like) are not essential unless otherwise specified. The same applies to numerical values and ranges thereof, and the present invention is not limited thereto.
In the present disclosure, numerical ranges indicated using “to” include numerical values described before and after “to” as the minimum value and the maximum value, respectively.
In the numerical ranges described stepwise in the present disclosure, the upper limit value or the lower limit value described in one numerical range may be replaced with the upper limit value or the lower limit value of another numerical description. . Further, in the numerical ranges described in the present disclosure, the upper limit value or the lower limit value of the numerical range may be replaced with the values shown in the examples.
In the present disclosure, each component may contain a plurality of corresponding substances. When multiple types of substances corresponding to each component are present in the composition, the content or content of each component is the total content or content of the multiple types of substances present in the composition unless otherwise specified. Means quantity.
In the present disclosure, a plurality of particles corresponding to each component may be included. When a plurality of particles corresponding to each component are present in the composition, the particle diameter of each component means a value for a mixture of the plurality of particles present in the composition unless otherwise specified.
In the present disclosure, the term “layer” or “film” includes only a part of the region in addition to the case where the layer or film is formed over the entire region. The case where it is formed is also included.
In the present disclosure, the term “lamination” indicates that layers are stacked, and two or more layers may be combined, or two or more layers may be detachable.
In the present disclosure, “(meth) acryloyl” means at least one of acryloyl and methacryloyl, “(meth) acrylate” means at least one of acrylate and methacrylate, and “(meth) allyl” means allyl and methallyl. Means at least one.
In the present disclosure, a compound containing both a thiol group and an alkyleneoxy group is classified as a thiol compound.
In the present disclosure, a structure in which an oxygen atom of an ester bond and a carbon atom adjacent to the oxygen atom are bonded (—O—R in —C (═O) —O—R, R represents a substituent), In addition, a structure in which an oxygen atom of a hydroxyl group and a carbon atom adjacent to the oxygen atom are bonded (O—R in HO—R, R represents a substituent) is not classified as an alkyleneoxy group.
＜波長変換部材＞
　本開示の波長変換部材は、量子ドット蛍光体を含み、アルキレンオキシ構造を有する硬化物を備える。本開示の波長変換部材は、必要に応じて、後述する被覆材等のその他の構成要素を含んでいてもよい。
　本開示の硬化物は、後述する本開示の硬化性組成物の硬化物であってもよい。
　本開示の波長変換部材は、画像表示用として好適に用いられる。 <Wavelength conversion member>
The wavelength conversion member of the present disclosure includes a cured product including a quantum dot phosphor and having an alkyleneoxy structure. The wavelength conversion member of the present disclosure may include other components such as a coating material to be described later as necessary.
The cured product of the present disclosure may be a cured product of the curable composition of the present disclosure described later.
The wavelength conversion member of the present disclosure is suitably used for image display.
　本開示の波長変換部材は、硬化物がアルキレンオキシ構造を有することにより、高温高湿環境下に晒された場合であっても量子ドット蛍光体の劣化の指標となる相対発光強度保持率が改善し、耐湿熱性に優れる。これは、アルキレンオキシ構造により硬化物に極性が付与され、非極性の酸素が硬化物中の成分（例えば、樹脂成分）に溶解しにくくなっているため、量子ドット蛍光体に酸素が接触しにくくなり、量子ドットの酸化劣化が抑制されていることが理由であると推察される。なお、アルキレンオキシ構造は、例えば、後述する硬化性組成物に含まれるアルキレンオキシ基含有化合物におけるアルキレンオキシ基由来であってもよい。 The wavelength conversion member of the present disclosure has improved relative emission intensity retention, which is an indicator of deterioration of the quantum dot phosphor, even when exposed to a high temperature and high humidity environment because the cured product has an alkyleneoxy structure. And excellent in heat and humidity resistance. This is because polarity is imparted to the cured product by the alkyleneoxy structure, and nonpolar oxygen is difficult to dissolve in components (eg, resin components) in the cured product, so that it is difficult for oxygen to contact the quantum dot phosphor. Thus, the reason is that the oxidative deterioration of the quantum dots is suppressed. The alkyleneoxy structure may be derived, for example, from an alkyleneoxy group in an alkyleneoxy group-containing compound contained in the curable composition described later.
　また、硬化物中の成分がアルキレンオキシ構造を有することにより、硬化物中の成分と量子ドット蛍光体との相溶性が低下して硬化物が白濁しやすいため、硬化物に光散乱効果が付与される傾向にある。 In addition, since the component in the cured product has an alkyleneoxy structure, the compatibility between the component in the cured product and the quantum dot phosphor is reduced, and the cured product is likely to become cloudy, thus providing a light scattering effect to the cured product. Tend to be.
　また、本開示の波長変換部材では、量子ドット蛍光体の酸化劣化が好適に抑制されているため、硬化物中の量子ドット蛍光体の含有量を従来よりも少なくしても良好な発光強度が得られる傾向にある。 Further, in the wavelength conversion member of the present disclosure, since the oxidative deterioration of the quantum dot phosphor is suitably suppressed, even if the content of the quantum dot phosphor in the cured product is reduced as compared with the conventional case, a good emission intensity is obtained. It tends to be obtained.
　また、硬化物は、スルフィド構造を有することが好ましい。硬化物がスルフィド構造を有することにより、硬化物の極性向上に寄与し、非極性の酸素が硬化物中の成分に好適に溶解しにくくなる傾向にある。なお、スルフィド構造は、例えば、後述する硬化性組成物に含まれ得る多官能チオール化合物におけるチオール基と、炭素炭素二重結合等の重合性反応基を含む化合物（例えば、後述するアルキレンオキシ基含有化合物）における重合性反応基との重合反応により、形成されたものであってもよい。 The cured product preferably has a sulfide structure. When the cured product has a sulfide structure, it contributes to improving the polarity of the cured product, and non-polar oxygen tends to be difficult to dissolve suitably in the components in the cured product. The sulfide structure is, for example, a compound containing a thiol group in a polyfunctional thiol compound that can be included in the curable composition described later and a polymerizable reactive group such as a carbon-carbon double bond (for example, an alkyleneoxy group containing described later) It may be formed by a polymerization reaction with a polymerizable reactive group in the compound).
　また、硬化物は、脂環式構造を有していてもよい。
　硬化物に含まれる脂環式構造は特に限定されるものではない。脂環式構造の具体例としては、トリシクロデカン骨格、シクロヘキサン骨格、１，３－アダマンタン骨格、水添ビスフェノールＡ骨格、水添ビスフェノールＦ骨格、水添ビスフェノールＳ骨格、イソボルニル骨格等が挙げられる。これらの中でも、トリシクロデカン骨格又はイソボルニル骨格であることが好ましく、トリシクロデカン骨格であることがより好ましい。 Moreover, the cured product may have an alicyclic structure.
The alicyclic structure contained in the cured product is not particularly limited. Specific examples of the alicyclic structure include a tricyclodecane skeleton, a cyclohexane skeleton, a 1,3-adamantane skeleton, a hydrogenated bisphenol A skeleton, a hydrogenated bisphenol F skeleton, a hydrogenated bisphenol S skeleton, and an isobornyl skeleton. Among these, a tricyclodecane skeleton or an isobornyl skeleton is preferable, and a tricyclodecane skeleton is more preferable.
　硬化物に含まれる脂環式構造は、１種類単独であっても、少なくとも２種類であってもよい。
　少なくとも２種類の脂環式構造が硬化物に含まれる場合、脂環式構造の組み合わせとしては、トリシクロデカン骨格及びイソボルニル骨格の組み合わせ、水添ビスフェノールＡ骨格及びイソボルニル骨格の組み合わせ等が挙げられる。これらの中でも、トリシクロデカン骨格及びイソボルニル骨格の組み合わせが好ましい。 The alicyclic structure contained in the cured product may be one type alone or at least two types.
When at least two types of alicyclic structures are contained in the cured product, examples of combinations of alicyclic structures include a combination of a tricyclodecane skeleton and an isobornyl skeleton, a combination of a hydrogenated bisphenol A skeleton and an isobornyl skeleton, and the like. Among these, a combination of a tricyclodecane skeleton and an isobornyl skeleton is preferable.
　また、硬化物は、エステル構造を有していてもよい。なお、エステル構造は、例えば、後述する硬化性組成物に含まれるアルキレンオキシ基含有化合物中のエステル構造由来であってもよい。 The cured product may have an ester structure. The ester structure may be derived from, for example, an ester structure in an alkyleneoxy group-containing compound contained in the curable composition described later.
　本開示の波長変換部材は、硬化物におけるジヨードメタンの接触角及び水の接触角を用い、Ｗｕの式より算出される極性成分は、５ｍＪ／ｍ２～１２ｍＪ／ｍ２であることが好ましい。前述の極性成分が５ｍＪ／ｍ２以上であることにより、硬化物は極性が高く、非極性の酸素が硬化物中の成分に好適に溶解しにくくなっているため、高温高湿環境下にて硬化物中の量子ドット蛍光体の酸化劣化が好適に抑制される傾向にある。前述の極性成分が１２ｍＪ／ｍ２以下であることにより、硬化物のガラス転移温度が低下することに起因した硬化物の凝集力の低下を抑制でき、硬化物における酸素の透過性の上昇を好適に抑制できる傾向にある。なお、極性成分は、後述する実施例に記載されている方法にて測定すればよい。 The wavelength conversion member of the present disclosure uses the contact angle of diiodomethane and the contact angle of water in the cured product, and the polar component calculated from the Wu equation is preferably 5 mJ / m 2 to 12 mJ / m 2 . When the above-mentioned polar component is 5 mJ / m 2 or more, the cured product has a high polarity, and non-polar oxygen is not easily dissolved in the components in the cured product. There is a tendency that oxidative deterioration of the quantum dot phosphor in the cured product is suitably suppressed. When the aforementioned polar component is 12 mJ / m 2 or less, a decrease in the cohesive force of the cured product due to a decrease in the glass transition temperature of the cured product can be suppressed, and an increase in oxygen permeability in the cured product is preferable. It tends to be suppressed. In addition, what is necessary is just to measure a polar component by the method described in the Example mentioned later.
　前述の極性成分は、耐湿熱性にさらに優れる点から、５．５ｍＪ／ｍ２～１１ｍＪ／ｍ２であることが好ましく、６．０ｍＪ／ｍ２～１０．５ｍＪ／ｍ２であることがより好ましく、６．０ｍＪ／ｍ２～１０ｍＪ／ｍ２であることがさらに好ましい。 Polar components described above, from the viewpoint of further excellent wet heat resistance is preferably 5.5mJ / m 2 ~ 11mJ / m 2, more preferably from 6.0mJ / m 2 ~ 10.5mJ / m 2 6.0 mJ / m 2 to 10 mJ / m 2 is more preferable.
　本開示の波長変換部材は、温度４０℃かつ相対湿度７０％の条件下での硬化物の透湿度が２０ｇ／ｍ２・ｄａｙ以上であることが好ましい。前述の透湿度がある一定の値以上であることにより、硬化物は極性が高く、非極性の酸素が硬化物中の成分に好適に溶解しにくくなっているため、高温高湿環境下にて硬化物中の量子ドット蛍光体の酸化劣化が好適に抑制される傾向にある。さらに、透湿度がある一定の値以上の硬化物は水分を吸着しやすく、水分を吸着することで硬化物の極性がより高くなり、非極性の酸素が硬化物中の成分により溶解しにくくなるため、量子ドット蛍光体の酸化劣化が好適に抑制されていることも推測される。 The wavelength conversion member of the present disclosure preferably has a moisture permeability of 20 g / m 2 · day or more under the conditions of a temperature of 40 ° C. and a relative humidity of 70%. Since the moisture permeability mentioned above is a certain value or more, the cured product has high polarity, and non-polar oxygen is not easily dissolved in the components in the cured product. There is a tendency that oxidative deterioration of the quantum dot phosphor in the cured product is suitably suppressed. Furthermore, a cured product having a moisture permeability of a certain value or more is likely to adsorb moisture, and by adsorbing moisture, the polarity of the cured product becomes higher, and nonpolar oxygen is less likely to be dissolved by components in the cured product. Therefore, it is presumed that the oxidative deterioration of the quantum dot phosphor is suitably suppressed.
　温度４０℃かつ相対湿度７０％の条件下での硬化物の透湿度は、後述する実施例に記載されているように、ＪＩＳ　Ｚ　０２０８：１９７６の測定法に準拠して測定することができる。 The moisture permeability of the cured product under the conditions of a temperature of 40 ° C. and a relative humidity of 70% can be measured according to the measurement method of JIS Z 0208: 1976 as described in the examples described later.
　前述の透湿度は、発光強度の低下がより好適に抑制される点から、３０ｇ／ｍ２・ｄａｙ以上であることがより好ましく、４０ｇ／ｍ２・ｄａｙ以上であることがさらに好ましく、５０ｇ／ｍ２・ｄａｙ以上であることが特に好ましく、６０ｇ／ｍ２・ｄａｙ以上であることがより一層好ましい。 The above-mentioned moisture permeability is more preferably 30 g / m 2 · day or more, further preferably 40 g / m 2 · day or more, more preferably 50 g / m 2 · day or more, from the viewpoint that the decrease in emission intensity is more suitably suppressed. particularly preferably m is 2 · day or more, and still more preferably 60 g / m 2 · day or more.
　また、前述の透湿度は、硬化物の凝集力低下による酸素の透過性上昇を抑制する点から、２５０ｇ／ｍ２・ｄａｙ以下であることが好ましく、２１０ｇ／ｍ２・ｄａｙ以下であることがより好ましく、１８０ｇ／ｍ２・ｄａｙ以下であることがさらに好ましく、１５０ｇ／ｍ２・ｄａｙ以下であることが特に好ましい。 The moisture permeability is preferably 250 g / m 2 · day or less, more preferably 210 g / m 2 · day or less, from the viewpoint of suppressing an increase in oxygen permeability due to a decrease in cohesive strength of the cured product. More preferably, it is more preferably 180 g / m 2 · day or less, and particularly preferably 150 g / m 2 · day or less.
　フーリエ変換赤外分光光度計で測定した硬化物における、Ｃ＝Ｃ伸縮振動に帰属されるピーク面積（Ｖ１）と、Ｓ－Ｈ伸縮振動に帰属されるピーク面積（Ｖ２）との比率（Ｖ１／Ｖ２）は、０．０００５２以下であることが好ましく、０．０００１以下であることがより好ましく、０．００００９以下であることがさらに好ましい。
　なお、比率（Ｖ１／Ｖ２）は、０．００００１以上であってもよく、０．００００３以上であってもよく、０．００００４以上であってもよい。
　硬化物が、チオール基を含む化合物（例えば、多官能チオール化合物）におけるチオール基と炭素炭素二重結合を含む化合物（例えば、後述するアルキレンオキシ基含有化合物）における炭素炭素二重結合との重合反応により形成されたものである場合、比率（Ｖ１／Ｖ２）が小さいことは即ち、重合反応に寄与していないチオール基が多いことを示唆する。重合反応に寄与していないチオール基がある程度存在すると、未反応のチオール基が量子ドット蛍光体に配位して量子ドット蛍光体の劣化が抑制される傾向にある。
　一方、重合反応に寄与していないチオール基が多いと、硬化物のガラス転移温度が小さくなる傾向にあるため、硬化物の凝集力低下により酸素の透過性が上昇する傾向があるが、硬化物の加工性に優れる傾向にある。
　硬化物における、Ｃ＝Ｃ伸縮振動に帰属されるピーク面積（Ｖ１）及びＳ－Ｈ伸縮振動に帰属されるピーク面積（Ｖ２）は、フーリエ変換赤外分光光度計を用いて下記方法により測定された値をいう。
　ＦＴ－ＩＲ　Ｓｐｅｃｔｒｏｍｅｔｅｒ（Ｐｅｒｋｉｎ　Ｅｌｍｅｒ社）を用いて、測定対象の波長変換部材の表面をＡＴＲ（Ａｔｔｅｎｕａｔｅｄ　Ｔｏｔａｌ　Ｒｅｆｌｅｃｔｉｏｎ（全反射測定法））分析する。バックグラウンド測定は、空気で測定し、積算回数１６回の条件でＦＴ－ＩＲ測定を実施する。波長変換部材が被覆材を有する場合、被覆材を剥離した状態の波長変換部材の硬化物をＦＴ－ＩＲ測定に供する。 In a cured product measured with a Fourier transform infrared spectrophotometer, a ratio (V1 /) of a peak area (V1) attributed to C = C stretching vibration and a peak area (V2) attributed to SH stretching vibration in a cured product. V2) is preferably 0.00052 or less, more preferably 0.0001 or less, and further preferably 0.00009 or less.
The ratio (V1 / V2) may be 0.00001 or more, 0.00003 or more, or 0.00004 or more.
Polymerization reaction between a thiol group in a compound containing a thiol group (for example, a polyfunctional thiol compound) and a carbon-carbon double bond in a compound containing a carbon-carbon double bond (for example, an alkyleneoxy group-containing compound described later). In other words, the small ratio (V1 / V2) indicates that there are many thiol groups not contributing to the polymerization reaction. When a thiol group that does not contribute to the polymerization reaction is present to some extent, the unreacted thiol group is coordinated to the quantum dot phosphor and the deterioration of the quantum dot phosphor tends to be suppressed.
On the other hand, if there are many thiol groups that do not contribute to the polymerization reaction, the glass transition temperature of the cured product tends to decrease, so the oxygen permeability tends to increase due to the reduced cohesive strength of the cured product. It tends to be excellent in workability.
In the cured product, the peak area (V1) attributed to C = C stretching vibration and the peak area (V2) attributed to SH stretching vibration were measured by the following method using a Fourier transform infrared spectrophotometer. Value.
Using an FT-IR Spectrometer (Perkin Elmer), the surface of the wavelength conversion member to be measured is subjected to ATR (Attenuated Total Reflection) analysis. The background measurement is performed with air, and FT-IR measurement is performed under the condition of 16 integrations. When the wavelength conversion member has a coating material, the cured product of the wavelength conversion member in a state where the coating material is peeled is subjected to FT-IR measurement.
　硬化物は、白色顔料を含んでいてもよい。硬化物に含まれる白色顔料についての詳細は、後述の硬化性組成物の項に記載のとおりである。
　また、硬化物に含まれる量子ドット蛍光体についての詳細も、後述の硬化性組成物の項に記載のとおりである。 The cured product may contain a white pigment. The details of the white pigment contained in the cured product are as described in the section of the curable composition described later.
The details of the quantum dot phosphor contained in the cured product are also as described in the section of the curable composition described later.
　波長変換部材の形状は特に制限されず、フィルム状、レンズ状等が挙げられる。波長変換部材を後述するバックライトユニットに適用する場合には、波長変換部材はフィルム状であることが好ましい。 The shape of the wavelength conversion member is not particularly limited, and examples thereof include a film shape and a lens shape. When the wavelength conversion member is applied to a backlight unit described later, the wavelength conversion member is preferably a film.
　硬化物がフィルム状である場合、硬化物の平均厚みは、例えば、５０μｍ～２００μｍであることが好ましく、５０μｍ～１５０μｍであることがより好ましく、８０μｍ～１２０μｍであることがさらに好ましい。平均厚みが５０μｍ以上であると、波長変換効率がより向上する傾向にあり、平均厚みが２００μｍ以下であると、後述するバックライトユニットに適用した場合に、バックライトユニットをより薄型化できる傾向にある。
　フィルム状の硬化物の平均厚みは、例えば、マイクロメータを用いる、あるいは、ＳＥＭ（走査型電子顕微鏡）を用いて硬化物の断面を観察し、測定した任意の３箇所の厚みの算術平均値として求められる。
　また、フィルム状かつ複数層の波長変換部材から硬化物の平均厚みを求める場合、波長変換部材の平均厚み及び波長変換部材における硬化物以外の平均厚み（例えば、被覆材の平均厚み）をマイクロメータを用いて前述のようにして求め、波長変換部材の平均厚みから波長変換部材における硬化物以外の平均厚みを差し引いてもよい。
　また、フィルム状かつ複数層の波長変換部材から硬化物の平均厚みを求める場合、硬化物の平均厚みは、反射分光膜厚計等を用いる、あるいはＳＥＭ（走査型電子顕微鏡）を用いて硬化物の断面を観察し、測定した任意の３箇所の厚みの算術平均値として求められる。 When the cured product is a film, the average thickness of the cured product is, for example, preferably 50 μm to 200 μm, more preferably 50 μm to 150 μm, and even more preferably 80 μm to 120 μm. When the average thickness is 50 μm or more, the wavelength conversion efficiency tends to be further improved, and when the average thickness is 200 μm or less, the backlight unit tends to be thinner when applied to the backlight unit described later. is there.
The average thickness of the film-like cured product is, for example, as an arithmetic average value of thicknesses measured at arbitrary three locations using a micrometer or by observing a cross section of the cured product using an SEM (scanning electron microscope). Desired.
Moreover, when calculating | requiring the average thickness of hardened | cured material from a film-form and several layers wavelength conversion member, the average thickness (for example, average thickness of coating | covering material) other than hardened | cured material in the wavelength conversion member and the wavelength conversion member is micrometer The average thickness of the wavelength conversion member other than the cured product may be subtracted from the average thickness of the wavelength conversion member.
Moreover, when calculating | requiring the average thickness of hardened | cured material from a film-form and multiple layers wavelength conversion member, the average thickness of hardened | cured material uses a reflection spectral film thickness meter etc., or hardened | cured material using SEM (scanning electron microscope). It is calculated | required as an arithmetic average value of the thickness of arbitrary three places which observed the cross section of and measured.
　波長変換部材は、１種類の硬化性組成物を硬化したものであってもよく、２種類以上の硬化性組成物を硬化したものであってもよい。例えば、波長変換部材がフィルム状である場合、波長変換部材は、第１の量子ドット蛍光体を含む硬化性組成物を硬化した第１の硬化物と、第１の量子ドット蛍光体とは発光特性が異なる第２の量子ドット蛍光体を含む硬化性組成物を硬化した第２の硬化物とが積層されたものであってもよい。 The wavelength conversion member may be one obtained by curing one type of curable composition, or may be one obtained by curing two or more types of curable compositions. For example, when the wavelength conversion member is in the form of a film, the wavelength conversion member emits light from the first cured product obtained by curing the curable composition containing the first quantum dot phosphor and the first quantum dot phosphor. A laminate of a second cured product obtained by curing a curable composition containing second quantum dot phosphors having different characteristics may be used.
　波長変換部材は、硬化性組成物の塗膜、成形体等を形成し、必要に応じて乾燥処理を行った後、紫外線等の活性エネルギー線を照射することにより得ることができる。活性エネルギー線の波長及び照射量は、硬化性組成物の組成に応じて適宜設定することができる。一態様では、２８０ｎｍ～４００ｎｍの波長の紫外線を１００ｍＪ／ｃｍ２～５０００ｍＪ／ｃｍ２の照射量で照射する。紫外線源としては、低圧水銀灯、中圧水銀灯、高圧水銀灯、超高圧水銀灯、カーボンアーク灯、メタルハライドランプ、キセノンランプ、ケミカルランプ、ブラックライトランプ、マイクロウェーブ励起水銀灯等が挙げられる。 The wavelength conversion member can be obtained by irradiating an active energy ray such as an ultraviolet ray after forming a coating film, a molded product or the like of the curable composition and performing a drying treatment as necessary. The wavelength and irradiation amount of the active energy ray can be appropriately set according to the composition of the curable composition. In one aspect, it is irradiated with ultraviolet rays having a wavelength of 280 nm ~ 400 nm at an irradiation amount of 100mJ / cm 2 ~ 5000mJ / cm 2. Examples of the ultraviolet light source include a low-pressure mercury lamp, a medium-pressure mercury lamp, a high-pressure mercury lamp, an ultrahigh-pressure mercury lamp, a carbon arc lamp, a metal halide lamp, a xenon lamp, a chemical lamp, a black light lamp, and a microwave-excited mercury lamp.
　また、硬化物は、密着性及び加工性をより向上させる観点から、ガラス転移温度（Ｔｇ）が４７℃以下であることが好ましく、０℃～４７℃であることがより好ましく、１０℃～４７℃であることがさらに好ましく、１５℃～２１℃であることが特に好ましい。硬化物のガラス転移温度（Ｔｇ）は、動的粘弾性測定装置（例えば、Ｒｈｅｏｍｅｔｒｉｃ　Ｓｃｉｅｎｔｉｆｉｃ社、Ｓｏｌｉｄ　Ａｎａｌｙｚｅｒ　ＲＳＡ－ＩＩＩ）を用いて、周波数１０Ｈｚの条件で測定することができる。 In addition, the cured product preferably has a glass transition temperature (Tg) of 47 ° C. or lower, more preferably 0 ° C. to 47 ° C., and more preferably 10 ° C. to 47 ° C. from the viewpoint of further improving adhesion and workability. More preferably, the temperature is 15 ° C. to 21 ° C. The glass transition temperature (Tg) of the cured product can be measured using a dynamic viscoelasticity measuring device (for example, Rheometric Scientific, Solid Analyzer RSA-III) under the condition of a frequency of 10 Hz.
　また、硬化物は、密着性及び耐熱性を向上させる観点から、周波数１０Ｈｚかつ温度２５℃の条件で測定した貯蔵弾性率が１×１０３Ｐａ～１×１０１０Ｐａであることが好ましく、１×１０４Ｐａ～１×１０９Ｐａであることがより好ましく、１×１０５Ｐａ～１×１０７Ｐａであることがさらに好ましい。硬化物の貯蔵弾性率は、動的粘弾性測定装置（例えば、Ｒｈｅｏｍｅｔｒｉｃ　Ｓｃｉｅｎｔｉｆｉｃ社、Ｓｏｌｉｄ　Ａｎａｌｙｚｅｒ　ＲＳＡ－ＩＩＩ）を用いて測定することができる。 The cured product preferably has a storage elastic modulus of 1 × 10 3 Pa to 1 × 10 10 Pa measured under conditions of a frequency of 10 Hz and a temperature of 25 ° C. from the viewpoint of improving adhesion and heat resistance. More preferably, it is from x10 4 Pa to 1 x 10 9 Pa, and even more preferably from 1 x 10 5 Pa to 1 x 10 7 Pa. The storage elastic modulus of the cured product can be measured using a dynamic viscoelasticity measuring device (for example, Rheometric Scientific, Solid Analyzer RSA-III).
　本開示の波長変換部材は、硬化物の少なくとも一部を被覆する被覆材をさらに有していてもよい。例えば、硬化物がフィルム状である場合、フィルム状の硬化物の片面又は両面がフィルム状の被覆材によって被覆されていてもよい。 The wavelength conversion member of the present disclosure may further include a covering material that covers at least a part of the cured product. For example, when the cured product is in the form of a film, one side or both sides of the film-like cured product may be covered with a film-shaped coating material.
　被覆材は、量子ドット蛍光体の発光効率の低下を抑える観点から、酸素に対するバリア性を有することが好ましい。 It is preferable that the coating material has a barrier property against oxygen from the viewpoint of suppressing a decrease in light emission efficiency of the quantum dot phosphor.
　また、本開示の波長変換部材は、硬化物は極性が高く、非極性の酸素が硬化物中の成分（例えば、樹脂成分）に溶解しにくくなっていると考えられるため、後述の無機層を有するバリアフィルムよりも酸素に対するバリア性の低い被覆材を有する構成であってもよい。 In addition, since the wavelength conversion member of the present disclosure is considered that the cured product has high polarity and nonpolar oxygen is hardly dissolved in a component (for example, a resin component) in the cured product, an inorganic layer described later is provided. The structure which has a coating | coated material with a barrier property with respect to oxygen lower than the barrier film to have may be sufficient.
　波長変換部材が被覆材を有する場合、被覆材の材質は、特に制限されない。例えば、樹脂が挙げられる。樹脂の種類は特に制限されず、ポリエチレンテレフタレート（ＰＥＴ）、ポリエチレンナフタレート（ＰＥＮ）等のポリエステル、ポリエチレン（ＰＥ）、ポリプロピレン（ＰＰ）等のポリオレフィン、ナイロン等のポリアミド、エチレン－ビニルアルコール共重合体（ＥＶＯＨ）などが挙げられる。また、被覆材は、バリア機能を高めるためのバリア層を備えたもの（バリアフィルム）であってもよい。バリア層としては、アルミナ、シリカ等の無機物を含む無機層が挙げられる。 When the wavelength conversion member has a coating material, the material of the coating material is not particularly limited. For example, resin is mentioned. The type of resin is not particularly limited, polyester such as polyethylene terephthalate (PET) and polyethylene naphthalate (PEN), polyolefin such as polyethylene (PE) and polypropylene (PP), polyamide such as nylon, and ethylene-vinyl alcohol copolymer (EVOH) and the like. Further, the covering material may be one (barrier film) provided with a barrier layer for enhancing the barrier function. Examples of the barrier layer include inorganic layers containing inorganic substances such as alumina and silica.
　被覆材は単層構造でも複層構造であってもよい。複層構造である場合は、材質の異なる２以上の層の組み合わせであってもよい。 The covering material may be a single layer structure or a multilayer structure. In the case of a multilayer structure, a combination of two or more layers having different materials may be used.
　被覆材がフィルム状である場合、被覆材の平均厚みは、例えば、８０μｍ～１５０μｍであることが好ましく、１００μｍ～１４０μｍであることがより好ましく、１００μｍ～１３５μｍであることがさらに好ましい。平均厚みが８０μｍ以上であると、バリア性等の機能が充分なものとなる傾向にあり、平均厚みが１５０μｍ以下であると、光透過率の低下が抑えられる傾向にある。
　フィルム状の被覆材の平均厚みは、フィルム状の波長変換部材の平均厚みと同様にして求められる。 When the coating material is in the form of a film, the average thickness of the coating material is, for example, preferably 80 μm to 150 μm, more preferably 100 μm to 140 μm, and even more preferably 100 μm to 135 μm. When the average thickness is 80 μm or more, functions such as barrier properties tend to be sufficient, and when the average thickness is 150 μm or less, a decrease in light transmittance tends to be suppressed.
The average thickness of the film-shaped coating material is obtained in the same manner as the average thickness of the film-shaped wavelength conversion member.
　波長変換部材の信頼性を維持しつつ低コスト化を図る観点からは、被覆材はＥＶＯＨを含むことが好ましい。ＥＶＯＨを含む被覆材は、樹脂基材と無機層とからなるバリアフィルムよりも水バリア性に劣る傾向にあるが、樹脂の中でも酸素透過率が特に低いため、量子ドット蛍光体の劣化を抑制するのに充分な酸素バリア性を有する。 From the viewpoint of cost reduction while maintaining the reliability of the wavelength conversion member, the coating material preferably contains EVOH. The coating material containing EVOH tends to be inferior to the water barrier property than the barrier film composed of the resin base material and the inorganic layer, but suppresses deterioration of the quantum dot phosphor because the oxygen permeability is particularly low among the resins. It has a sufficient oxygen barrier property.
　ＥＶＯＨにおけるエチレンに由来する構造単位の割合（エチレン含有率）は特に制限されず、波長変換部材の所望の特性等を考慮して選択できる。酸素バリア性の観点からは、エチレン含有率が小さいことが好ましく、強度及び耐水性の観点からは、エチレン含有率が大きいことが好ましい。例えば、ＥＶＯＨにおけるエチレン含有率は２０モル％～５０モル％であることが好ましく、２５モル％～４５モル％であることがより好ましく、３０モル％～４０モル％であることがさらに好ましい。 The proportion of ethylene-derived structural units (ethylene content) in EVOH is not particularly limited, and can be selected in consideration of the desired characteristics of the wavelength conversion member. From the viewpoint of oxygen barrier properties, the ethylene content is preferably small, and from the viewpoint of strength and water resistance, the ethylene content is preferably large. For example, the ethylene content in EVOH is preferably 20 mol% to 50 mol%, more preferably 25 mol% to 45 mol%, and even more preferably 30 mol% to 40 mol%.
　ＥＶＯＨを含む被覆材の平均厚みは、例えば、２０μｍ以上であることが好ましく、５０μｍ以上であることがより好ましい。平均厚みが２０μｍ以上であると、バリア性等の機能が充分なものとなる傾向にある。
　ＥＶＯＨを含む被覆材の平均厚みは、例えば、１５０μｍ以下であることが好ましく、１２５μｍ以下であることがより好ましい。平均厚みが１５０μｍ以下であると、光透過率の低下が抑えられる傾向にある。 The average thickness of the covering material containing EVOH is, for example, preferably 20 μm or more, and more preferably 50 μm or more. When the average thickness is 20 μm or more, functions such as barrier properties tend to be sufficient.
The average thickness of the covering material containing EVOH is, for example, preferably 150 μm or less, and more preferably 125 μm or less. When the average thickness is 150 μm or less, a decrease in light transmittance tends to be suppressed.
　被覆材の酸素透過率は、例えば、０．５ｃｍ３／（ｍ２・ｄａｙ・ａｔｍ）以下であることが好ましく、０．３ｃｍ３／（ｍ２・ｄａｙ・ａｔｍ）以下であることがより好ましく、０．１ｃｍ３／（ｍ２・ｄａｙ・ａｔｍ）以下であることがさらに好ましい。 The oxygen permeability of the covering material is, for example, preferably 0.5 cm 3 / (m 2 · day · atm) or less, and more preferably 0.3 cm 3 / (m 2 · day · atm) or less. More preferably, it is 0.1 cm 3 / (m 2 · day · atm) or less.
　被覆材の酸素透過率は、酸素透過率測定装置（例えば、ＭＯＣＯＮ社、ＯＸ－ＴＲＡＮ）を用いて、２０℃、相対湿度６５％の条件で測定することができる。 The oxygen permeability of the coating material can be measured under the conditions of 20 ° C. and 65% relative humidity using an oxygen permeability measuring device (for example, MOCON, OX-TRAN).
　被覆材の水蒸気透過率の上限値は特に制限されないが、例えば、１×１０－１ｇ／（ｍ２・ｄａｙ）以下であってもよい。 The upper limit value of the water vapor transmission rate of the coating material is not particularly limited, but may be, for example, 1 × 10 −1 g / (m 2 · day) or less.
　被覆材の水蒸気透過率は、水蒸気透過率測定装置（例えば、ＭＯＣＯＮ社、ＡＱＵＡＴＲＡＮ）を用いて４０℃、相対湿度９０％の環境下で測定することができる。 The water vapor transmission rate of the coating material can be measured in an environment of 40 ° C. and 90% relative humidity using a water vapor transmission rate measuring device (for example, MOCON, AQUATRAN).
　本開示の波長変換部材は、光の利用効率をより向上させる観点から、全光線透過率が５５％以上であることが好ましく、６０％以上であることがより好ましく、６５％以上であることがさらに好ましい。波長変換部材の全光線透過率は、ＪＩＳ　Ｋ　７１３６：２０００の測定法に準拠して測定することができる。 The wavelength conversion member of the present disclosure has a total light transmittance of preferably 55% or more, more preferably 60% or more, and more preferably 65% or more from the viewpoint of further improving the light utilization efficiency. Further preferred. The total light transmittance of the wavelength conversion member can be measured in accordance with the measurement method of JIS K 7136: 2000.
　また、本開示の波長変換部材は、光の利用効率をより向上させる観点から、ヘーズが９５％以上であることが好ましく、９７％以上であることがより好ましく、９９％以上であることがさらに好ましい。波長変換部材のヘーズは、ＪＩＳ　Ｋ　７１３６：２０００の測定法に準拠して測定することができる。 Further, in the wavelength conversion member of the present disclosure, from the viewpoint of further improving the light utilization efficiency, the haze is preferably 95% or more, more preferably 97% or more, and further preferably 99% or more. preferable. The haze of the wavelength conversion member can be measured in accordance with the measurement method of JIS K 7136: 2000.
　波長変換部材の概略構成の一例を図１に示す。但し、本開示の波長変換部材は図１の構成に限定されるものではない。また、図１における硬化物及び被覆材の大きさは概念的なものであり、大きさの相対的な関係はこれに限定されない。なお、各図面において、同一の部材には同一の符号を付し、重複した説明は省略することがある。 An example of a schematic configuration of the wavelength conversion member is shown in FIG. However, the wavelength conversion member of the present disclosure is not limited to the configuration of FIG. Moreover, the magnitude | size of the hardened | cured material in FIG. 1 and a coating | covering material is notional, and the relative relationship of a magnitude | size is not limited to this. In addition, in each drawing, the same code | symbol is attached | subjected to the same member and the overlapping description may be abbreviate | omitted.
　図１に示す波長変換部材１０は、フィルム状の硬化物である硬化物１１と、硬化物１１の両面に設けられたフィルム状の被覆材１２Ａ及び１２Ｂとを有する。被覆材１２Ａ及び被覆材１２Ｂの種類及び平均厚みは、それぞれ同一であっても異なっていてもよい。 1 includes a cured product 11 that is a film-like cured product, and film-shaped coating materials 12A and 12B that are provided on both surfaces of the cured product 11. The types and average thicknesses of the covering material 12A and the covering material 12B may be the same or different.
　図１に示す構成の波長変換部材は、例えば、以下のような公知の製造方法により製造することができる。 1 can be manufactured by, for example, the following known manufacturing method.
　まず、連続搬送されるフィルム状の被覆材（以下、「第１の被覆材」ともいう。）の表面に後述の硬化性組成物を付与し、塗膜を形成する。硬化性組成物の付与方法は特に制限されず、ダイコーティング法、カーテンコーティング法、エクストルージョンコーティング法、ロッドコーティング法、ロールコーティング法等が挙げられる。 First, a coating composition is formed by applying a curable composition described later to the surface of a film-like coating material (hereinafter also referred to as “first coating material”) that is continuously conveyed. A method for applying the curable composition is not particularly limited, and examples thereof include a die coating method, a curtain coating method, an extrusion coating method, a rod coating method, and a roll coating method.
　次いで、硬化性組成物の塗膜の上に、連続搬送されるフィルム状の被覆材（以下、「第２の被覆材」ともいう。）を貼り合わせる。 Next, a film-like coating material (hereinafter also referred to as “second coating material”) that is continuously conveyed is bonded onto the coating film of the curable composition.
　次いで、第１の被覆材及び第２の被覆材のうち活性エネルギー線を透過可能な被覆材側から活性エネルギー線を照射することにより、塗膜を硬化し、硬化物を形成する。その後、規定のサイズに切り出すことにより、図１に示す構成の波長変換部材を得ることができる。 Next, by irradiating active energy rays from the side of the first covering material and the second covering material that can transmit active energy rays, the coating film is cured to form a cured product. Then, the wavelength conversion member of the structure shown in FIG. 1 can be obtained by cutting out to a regular size.
　なお、第１の被覆材及び第２の被覆材のいずれも活性エネルギー線を透過可能でない場合には、第２の被覆材を貼り合わせる前に塗膜に活性エネルギー線を照射し、硬化物を形成してもよい。 If neither the first coating material nor the second coating material can transmit active energy rays, the coating material is irradiated with active energy rays before the second coating material is bonded, and the cured product is removed. It may be formed.
＜バックライトユニット＞
　本開示のバックライトユニットは、上述した本開示の波長変換部材と、光源とを備える。 <Backlight unit>
The backlight unit of the present disclosure includes the above-described wavelength conversion member of the present disclosure and a light source.
　バックライトユニットとしては、色再現性を向上させる観点から、多波長光源化されたものが好ましい。好ましい一態様としては、４３０ｎｍ～４８０ｎｍの波長域に発光中心波長を有し、半値幅が１００ｎｍ以下である発光強度ピークを有する青色光と、５２０ｎｍ～５６０ｎｍの波長域に発光中心波長を有し、半値幅が１００ｎｍ以下である発光強度ピークを有する緑色光と、６００ｎｍ～６８０ｎｍの波長域に発光中心波長を有し、半値幅が１００ｎｍ以下である発光強度ピークを有する赤色光と、を発光するバックライトユニットを挙げることができる。なお、発光強度ピークの半値幅とは、ピーク高さの１／２の高さにおけるピーク幅であって半値全幅（Ｆｕｌｌ　Ｗｉｄｔｈ　ａｔ　Ｈａｌｆ　Ｍａｘｉｍｕｍ、ＦＷＨＭ）を意味する。 The backlight unit is preferably a multi-wavelength light source from the viewpoint of improving color reproducibility. As a preferred embodiment, blue light having an emission center wavelength in a wavelength range of 430 nm to 480 nm, an emission intensity peak having a half width of 100 nm or less, and an emission center wavelength in a wavelength range of 520 nm to 560 nm, Back light that emits green light having an emission intensity peak with a half-value width of 100 nm or less and red light having an emission center wavelength in a wavelength region of 600 to 680 nm and an emission intensity peak with a half-value width of 100 nm or less A light unit can be mentioned. The half-value width of the emission intensity peak means a peak width at half the peak height and a full width at half maximum (Full Width at Half Maximum, FWHM).
　色再現性をより向上させる観点から、バックライトユニットが発光する青色光の発光中心波長は、４４０ｎｍ～４７５ｎｍの範囲であることが好ましい。同様の観点から、バックライトユニットが発光する緑色光の発光中心波長は、５２０ｎｍ～５４５ｎｍの範囲であることが好ましい。また、同様の観点から、バックライトユニットが発光する赤色光の発光中心波長は、６１０ｎｍ～６４０ｎｍの範囲であることが好ましい。 From the viewpoint of further improving the color reproducibility, the emission center wavelength of the blue light emitted from the backlight unit is preferably in the range of 440 nm to 475 nm. From the same point of view, the emission center wavelength of the green light emitted from the backlight unit is preferably in the range of 520 nm to 545 nm. From the same viewpoint, the emission center wavelength of red light emitted from the backlight unit is preferably in the range of 610 nm to 640 nm.
　また、色再現性をより向上させる観点から、バックライトユニットが発光する青色光、緑色光、及び赤色光の各発光強度ピークの半値幅は、いずれも８０ｎｍ以下であることが好ましく、５０ｎｍ以下であることがより好ましく、４０ｎｍ以下であることがさらに好ましく、３０ｎｍ以下であることが特に好ましく、２５ｎｍ以下であることが極めて好ましい。 Further, from the viewpoint of further improving color reproducibility, the half-value widths of the emission intensity peaks of blue light, green light, and red light emitted by the backlight unit are all preferably 80 nm or less, and 50 nm or less. More preferably, it is more preferably 40 nm or less, particularly preferably 30 nm or less, and extremely preferably 25 nm or less.
　バックライトユニットの光源としては、例えば、４３０ｎｍ～４８０ｎｍの波長域に発光中心波長を有する青色光を発光する光源を用いることができる。光源としては、例えば、ＬＥＤ（Ｌｉｇｈｔ　Ｅｍｉｔｔｉｎｇ　Ｄｉｏｄｅ）及びレーザーが挙げられる。青色光を発光する光源を用いる場合、波長変換部材は、少なくとも、赤色光を発光する量子ドット蛍光体Ｒ及び緑色光を発光する量子ドット蛍光体Ｇを含むことが好ましい。これにより、波長変換部材から発光される赤色光及び緑色光と、波長変換部材を透過した青色光とにより、白色光を得ることができる。 As the light source of the backlight unit, for example, a light source that emits blue light having an emission center wavelength in a wavelength region of 430 nm to 480 nm can be used. Examples of the light source include an LED (Light Emitting Diode) and a laser. When using a light source that emits blue light, the wavelength conversion member preferably includes at least a quantum dot phosphor R that emits red light and a quantum dot phosphor G that emits green light. Thereby, white light can be obtained from the red light and green light emitted from the wavelength conversion member and the blue light transmitted through the wavelength conversion member.
　また、バックライトユニットの光源としては、例えば、３００ｎｍ～４３０ｎｍの波長域に発光中心波長を有する紫外光を発光する光源を用いることもできる。光源としては、例えば、ＬＥＤ及びレーザーが挙げられる。紫外光を発光する光源を用いる場合、波長変換部材は、量子ドット蛍光体Ｒ及び量子ドット蛍光体Ｇとともに、励起光により励起され青色光を発光する量子ドット蛍光体Ｂを含むことが好ましい。これにより、波長変換部材から発光される赤色光、緑色光、及び青色光により、白色光を得ることができる。 Further, as the light source of the backlight unit, for example, a light source that emits ultraviolet light having an emission center wavelength in a wavelength region of 300 nm to 430 nm can be used. Examples of the light source include an LED and a laser. When using a light source that emits ultraviolet light, the wavelength conversion member preferably includes a quantum dot phosphor B that emits blue light when excited by excitation light, together with the quantum dot phosphor R and the quantum dot phosphor G. Thereby, white light can be obtained from the red light, the green light, and the blue light emitted from the wavelength conversion member.
　本開示のバックライトユニットは、エッジライト方式であっても直下型方式であってもよい。 The backlight unit of the present disclosure may be an edge light type or a direct type.
　エッジライト方式のバックライトユニットの概略構成の一例を図２に示す。但し、本開示のバックライトユニットは、図２の構成に限定されるものではない。また、図２における部材の大きさは概念的なものであり、部材間の大きさの相対的な関係はこれに限定されない。 An example of a schematic configuration of an edge light type backlight unit is shown in FIG. However, the backlight unit of the present disclosure is not limited to the configuration of FIG. Moreover, the magnitude | size of the member in FIG. 2 is notional, The relative relationship of the magnitude | size between members is not limited to this.
　図２に示すバックライトユニット２０は、青色光ＬＢを出射する光源２１と、光源２１から出射された青色光ＬＢを導光して出射させる導光板２２と、導光板２２と対向配置される波長変換部材１０と、波長変換部材１０を介して導光板２２と対向配置される再帰反射性部材２３と、導光板２２を介して波長変換部材１０と対向配置される反射板２４とを備える。波長変換部材１０は、青色光ＬＢの一部を励起光として赤色光ＬＲ及び緑色光ＬＧを発光し、赤色光ＬＲ及び緑色光ＬＧと、励起光とならなかった青色光ＬＢとを出射する。この赤色光ＬＲ、緑色光ＬＧ、及び青色光ＬＢにより、再帰反射性部材２３から白色光ＬＷが出射される。 The backlight unit 20 shown in FIG. 2 includes a light source 21 for emitting the blue light L B, a light guide plate 22 to be emitted guiding the blue light L B emitted from the light source 21, the light guide plate 22 and disposed to face A wavelength conversion member 10, a retroreflective member 23 disposed opposite to the light guide plate 22 via the wavelength conversion member 10, and a reflection plate 24 disposed opposite to the wavelength conversion member 10 via the light guide plate 22. . Wavelength conversion member 10 emits the red light L R and the green light L G part of the blue light L B as the excitation light, the red light L and R and the green light L G, the blue light was not the excitation light L B is emitted. The red light L R, the green light L G, and the blue light L B, the white light L W is emitted from the retroreflective member 23.
＜画像表示装置＞
　本開示の画像表示装置は、上述した本開示のバックライトユニットを備える。画像表示装置としては特に制限されず、例えば、液晶表示装置が挙げられる。 <Image display device>
An image display device according to the present disclosure includes the above-described backlight unit according to the present disclosure. The image display device is not particularly limited, and examples thereof include a liquid crystal display device.
　液晶表示装置の概略構成の一例を図３に示す。但し、本開示の液晶表示装置は、図３の構成に限定されるものではない。また、図３における部材の大きさは概念的なものであり、部材間の大きさの相対的な関係はこれに限定されない。 An example of a schematic configuration of the liquid crystal display device is shown in FIG. However, the liquid crystal display device of the present disclosure is not limited to the configuration of FIG. Moreover, the magnitude | size of the member in FIG. 3 is notional, The relative relationship of the magnitude | size between members is not limited to this.
　図３に示す液晶表示装置３０は、バックライトユニット２０と、バックライトユニット２０と対向配置される液晶セルユニット３１とを備える。液晶セルユニット３１は、液晶セル３２が偏光板３３Ａと偏光板３３Ｂとの間に配置された構成とされる。 The liquid crystal display device 30 shown in FIG. 3 includes a backlight unit 20 and a liquid crystal cell unit 31 disposed to face the backlight unit 20. The liquid crystal cell unit 31 is configured such that the liquid crystal cell 32 is disposed between the polarizing plate 33A and the polarizing plate 33B.
　液晶セル３２の駆動方式は特に制限されず、ＴＮ（Ｔｗｉｓｔｅｄ　Ｎｅｍａｔｉｃ）方式、ＳＴＮ（Ｓｕｐｅｒ　Ｔｗｉｓｔｅｄ　Ｎｅｍａｔｉｃ）方式、ＶＡ（Ｖｉｒｔｉｃａｌ　Ａｌｉｇｎｍｅｎｔ）方式、ＩＰＳ（Ｉｎ－Ｐｌａｎｅ－Ｓｗｉｔｃｈｉｎｇ）方式、ＯＣＢ（Ｏｐｔｉｃａｌｌｙ　Ｃｏｍｐｅｎｓａｔｅｄ　Ｂｉｒｅｆｒｉｎｇｅｎｃｅ）方式等が挙げられる。 The driving method of the liquid crystal cell 32 is not particularly limited, and is a TN (Twisted Nematic) method, a STN (Super Twisted Nematic) method, a VA (Virtual Alignment) method, an IPS (In-Plane-Switching) method, and an OCB (Optically Filled). The method etc. are mentioned.
＜硬化性組成物＞
　本開示の硬化性組成物は、量子ドット蛍光体、アルキレンオキシ基及び重合性反応基を有するアルキレンオキシ基含有化合物（本開示では、単に「アルキレンオキシ基含有化合物」とも称する）、並びに光重合開始剤を含む。本開示の硬化性組成物は、上記構成を有することにより、硬化物の耐湿熱性に優れる。 <Curable composition>
The curable composition of the present disclosure includes a quantum dot phosphor, an alkyleneoxy group-containing compound having an alkyleneoxy group and a polymerizable reactive group (also simply referred to as “alkyleneoxy group-containing compound” in this disclosure), and photopolymerization initiation. Contains agents. The curable composition of this indication is excellent in the moist heat resistance of hardened | cured material by having the said structure.
　以下、本開示の硬化性組成物に含まれ得る成分について詳細に説明する。 Hereinafter, components that can be included in the curable composition of the present disclosure will be described in detail.
（量子ドット蛍光体）
　硬化性組成物は、量子ドット蛍光体を含む。量子ドット蛍光体としては特に制限されず、ＩＩ－ＶＩ族化合物、ＩＩＩ－Ｖ族化合物、ＩＶ－ＶＩ族化合物、及びＩＶ族化合物からなる群より選択される少なくとも１種を含む粒子が挙げられる。発光効率の観点からは、量子ドット蛍光体は、Ｃｄ及びＩｎの少なくとも一方を含む化合物を含むことが好ましい。 (Quantum dot phosphor)
The curable composition includes a quantum dot phosphor. The quantum dot phosphor is not particularly limited, and examples thereof include particles containing at least one selected from the group consisting of II-VI group compounds, III-V group compounds, IV-VI group compounds, and IV group compounds. From the viewpoint of luminous efficiency, the quantum dot phosphor preferably contains a compound containing at least one of Cd and In.
　ＩＩ－ＶＩ族化合物の具体例としては、ＣｄＳｅ、ＣｄＴｅ、ＣｄＳ、ＺｎＳ、ＺｎＳｅ、ＺｎＴｅ、ＺｎＯ、ＨｇＳ、ＨｇＳｅ、ＨｇＴｅ、ＣｄＳｅＳ、ＣｄＳｅＴｅ、ＣｄＳＴｅ、ＺｎＳｅＳ、ＺｎＳｅＴｅ、ＺｎＳＴｅ、ＨｇＳｅＳ、ＨｇＳｅＴｅ、ＨｇＳＴｅ、ＣｄＺｎＳ、ＣｄＺｎＳｅ、ＣｄＺｎＴｅ、ＣｄＨｇＳ、ＣｄＨｇＳｅ、ＣｄＨｇＴｅ、ＨｇＺｎＳ、ＨｇＺｎＳｅ、ＨｇＺｎＴｅ、ＣｄＺｎＳｅＳ、ＣｄＺｎＳｅＴｅ、ＣｄＺｎＳＴｅ、ＣｄＨｇＳｅＳ、ＣｄＨｇＳｅＴｅ、ＣｄＨｇＳＴｅ、ＨｇＺｎＳｅＳ、ＨｇＺｎＳｅＴｅ、ＨｇＺｎＳＴｅ等が挙げられる。
　ＩＩＩ－Ｖ族化合物の具体例としては、ＧａＮ、ＧａＰ、ＧａＡｓ、ＧａＳｂ、ＡｌＮ、ＡｌＰ、ＡｌＡｓ、ＡｌＳｂ、ＩｎＮ、ＩｎＰ、ＩｎＡｓ、ＩｎＳｂ、ＧａＮＰ、ＧａＮＡｓ、ＧａＮＳｂ、ＧａＰＡｓ、ＧａＰＳｂ、ＡｌＮＰ、ＡｌＮＡｓ、ＡｌＮＳｂ、ＡｌＰＡｓ、ＡｌＰＳｂ、ＩｎＮＰ、ＩｎＮＡｓ、ＩｎＮＳｂ、ＩｎＰＡｓ、ＩｎＰＳｂ、ＧａＡｌＮＰ、ＧａＡｌＮＡｓ、ＧａＡｌＮＳｂ、ＧａＡｌＰＡｓ、ＧａＡｌＰＳｂ、ＧａＩｎＮＰ、ＧａＩｎＮＡｓ、ＧａＩｎＮＳｂ、ＧａＩｎＰＡｓ、ＧａＩｎＰＳｂ、ＩｎＡｌＮＰ、ＩｎＡｌＮＡｓ、ＩｎＡｌＮＳｂ、ＩｎＡｌＰＡｓ、ＩｎＡｌＰＳｂ等が挙げられる。
　ＩＶ－ＶＩ族化合物の具体例としては、ＳｎＳ、ＳｎＳｅ、ＳｎＴｅ、ＰｂＳ、ＰｂＳｅ、ＰｂＴｅ、ＳｎＳｅＳ、ＳｎＳｅＴｅ、ＳｎＳＴｅ、ＰｂＳｅＳ、ＰｂＳｅＴｅ、ＰｂＳＴｅ、ＳｎＰｂＳ、ＳｎＰｂＳｅ、ＳｎＰｂＴｅ、ＳｎＰｂＳＳｅ、ＳｎＰｂＳｅＴｅ、ＳｎＰｂＳＴｅ等が挙げられる。
　ＩＶ族化合物の具体例としては、Ｓｉ、Ｇｅ、ＳｉＣ、ＳｉＧｅ等が挙げられる。 Specific examples of the II-VI group compounds include CdSe, CdTe, CdS, ZnS, ZnSe, ZnTe, ZnO, HgS, HgSe, HgTe, CdSeS, CdSeTe, CdSTe, ZnSeS, ZnSeTe, ZnSTe, HgSeS, HgSeS, HgSeT, CdZnSe, CdZnTe, CdHgS, CdHgSe, CdHgTe, HgZnS, HgZnSe, HgZnTe, CdZnSeS, CdZnSeTe, CdZnSTe, CdHgSeS, CdHgSeTe, GdHgSe, ST
Specific examples of the III-V group compounds include GaN, GaP, GaAs, GaSb, AlN, AlP, AlAs, AlSb, InN, InP, InAs, InSb, GNP, GANAS, GaNSb, GaPAs, GaPSb, AlNP, AlNAs, AlNSb. , AlPAs, AlPSb, InNP, InNAs, InNSb, InPAs, InPSb, GaAlNP, GaAlNAs, GaAlNSb, GaAlPAs, GaAlPSb, GaInNP, GaInNAs, GaInNSb, GaInPAs, GaInPSb, InAlNP, InAlNS, InAlNb, InAlNs, InAlNb, InAlNs, InAlNb, InAlNs, InAlNb, InAlNS
Specific examples of the IV-VI group compounds include SnS, SnSe, SnTe, PbS, PbSe, PbTe, SnSeS, SnSeTe, SnSTe, PbSeS, PbSeTe, PbSTe, SnPbS, SnPbSe, SnPbSe, SnPbTe, Sn, etc. .
Specific examples of the group IV compound include Si, Ge, SiC, SiGe and the like.
　量子ドット蛍光体としては、コアシェル構造を有するものが好ましい。コアを構成する化合物のバンドギャップよりもシェルを構成する化合物のバンドギャップを広くすることで、量子ドット蛍光体の量子効率をより向上させることが可能となる。コア及びシェルの組み合わせ（コア／シェル）としては、ＣｄＳｅ／ＺｎＳ、ＩｎＰ／ＺｎＳ、ＰｂＳｅ／ＰｂＳ、ＣｄＳｅ／ＣｄＳ、ＣｄＴｅ／ＣｄＳ、ＣｄＴｅ／ＺｎＳ等が挙げられる。 Quantum dot phosphors preferably have a core-shell structure. By making the band gap of the compound constituting the shell wider than the band gap of the compound constituting the core, the quantum efficiency of the quantum dot phosphor can be further improved. Examples of the combination of core and shell (core / shell) include CdSe / ZnS, InP / ZnS, PbSe / PbS, CdSe / CdS, CdTe / CdS, CdTe / ZnS, and the like.
　また、量子ドット蛍光体としては、シェルが多層構造である、いわゆるコアマルチシェル構造を有するものであってもよい。バンドギャップの広いコアにバンドギャップの狭いシェルを１層又は２層以上積層し、さらにこのシェルの上にバンドギャップの広いシェルを積層することで、量子ドット蛍光体の量子効率をさらに向上させることが可能となる。 Also, the quantum dot phosphor may have a so-called core multishell structure in which the shell has a multilayer structure. By stacking one or more shells with a narrow band gap on a core with a wide band gap, and further stacking a shell with a wide band gap on this shell, the quantum efficiency of the quantum dot phosphor can be further improved. Is possible.
　硬化性組成物は、１種類の量子ドット蛍光体を単独で含んでいてもよく、２種類以上の量子ドット蛍光体を組み合わせて含んでいてもよい。２種類以上の量子ドット蛍光体を組み合わせて含む態様としては、例えば、成分は異なるものの平均粒子径を同じくする量子ドット蛍光体を２種類以上含む態様、平均粒子径は異なるものの成分を同じくする量子ドット蛍光体を２種類以上含む態様、並びに成分及び平均粒子径の異なる量子ドット蛍光体を２種類以上含む態様が挙げられる。量子ドット蛍光体の成分及び平均粒子径の少なくとも一方を変更することで、量子ドット蛍光体の発光中心波長を変更することができる。 The curable composition may contain one kind of quantum dot phosphor alone, or may contain two or more kinds of quantum dot phosphors in combination. As an aspect including a combination of two or more types of quantum dot phosphors, for example, an aspect including two or more types of quantum dot phosphors having the same average particle diameter, although the components are different, and a quantum having the same components having different average particle diameters The aspect containing 2 or more types of dot fluorescent substance and the aspect containing 2 or more types of quantum dot fluorescent substance from which a component and an average particle diameter differ are mentioned. By changing at least one of the components of the quantum dot phosphor and the average particle diameter, the emission center wavelength of the quantum dot phosphor can be changed.
　例えば、硬化性組成物は、５２０ｎｍ～５６０ｎｍの緑色の波長域に発光中心波長を有する量子ドット蛍光体Ｇと、６００ｎｍ～６８０ｎｍの赤色の波長域に発光中心波長を有する量子ドット蛍光体Ｒとを含んでいてもよい。量子ドット蛍光体Ｇと量子ドット蛍光体Ｒとを含む硬化性組成物の硬化物に対して４３０ｎｍ～４８０ｎｍの青色の波長域の励起光を照射すると、量子ドット蛍光体Ｇ及び量子ドット蛍光体Ｒからそれぞれ緑色光及び赤色光が発光される。その結果、量子ドット蛍光体Ｇ及び量子ドット蛍光体Ｒから発光される緑色光及び赤色光と、硬化物を透過する青色光とにより、白色光を得ることができる。 For example, the curable composition comprises a quantum dot phosphor G having an emission center wavelength in the green wavelength region of 520 nm to 560 nm and a quantum dot phosphor R having an emission center wavelength in the red wavelength region of 600 nm to 680 nm. May be included. When the cured product of the curable composition including the quantum dot phosphor G and the quantum dot phosphor R is irradiated with excitation light in a blue wavelength region of 430 nm to 480 nm, the quantum dot phosphor G and the quantum dot phosphor R Respectively emit green light and red light. As a result, white light can be obtained by the green light and red light emitted from the quantum dot phosphor G and the quantum dot phosphor R and the blue light transmitted through the cured product.
　量子ドット蛍光体は、分散媒体に分散された量子ドット蛍光体分散液の状態で用いてもよい。量子ドット蛍光体を分散する分散媒体としては、水、各種有機溶剤及び単官能（メタ）アクリレート化合物が挙げられる。
　分散媒体として使用可能な有機溶剤としては、アセトン、酢酸エチル、トルエン、ｎ－ヘキサン等が挙げられる。
　分散媒体として使用可能な単官能（メタ）アクリレート化合物としては、室温（２５℃）において液体であれば特に限定されるものではなく、イソボルニル（メタ）アクリレート、ジシクロペンタニル（メタ）アクリレート等が挙げられる。
　これらの中でも、分散媒体としては、硬化性組成物を硬化する際に分散媒体を揮発させる工程が不要になる観点から、単官能（メタ）アクリレート化合物であることが好ましく、脂環式構造を有する単官能（メタ）アクリレート化合物であることがより好ましく、イソボルニル（メタ）アクリレート及びジシクロペンタニル（メタ）アクリレートであることがさらに好ましく、イソボルニル（メタ）アクリレートであることが特に好ましい。 The quantum dot phosphor may be used in the state of a quantum dot phosphor dispersion liquid dispersed in a dispersion medium. Examples of the dispersion medium for dispersing the quantum dot phosphor include water, various organic solvents, and a monofunctional (meth) acrylate compound.
Examples of the organic solvent that can be used as the dispersion medium include acetone, ethyl acetate, toluene, n-hexane, and the like.
The monofunctional (meth) acrylate compound that can be used as the dispersion medium is not particularly limited as long as it is liquid at room temperature (25 ° C.), and examples thereof include isobornyl (meth) acrylate and dicyclopentanyl (meth) acrylate. Can be mentioned.
Among these, the dispersion medium is preferably a monofunctional (meth) acrylate compound and has an alicyclic structure from the viewpoint that the step of volatilizing the dispersion medium when curing the curable composition is unnecessary. A monofunctional (meth) acrylate compound is more preferable, isobornyl (meth) acrylate and dicyclopentanyl (meth) acrylate are more preferable, and isobornyl (meth) acrylate is particularly preferable.
　分散媒体として単官能（メタ）アクリレート化合物を用いる場合、単官能（メタ）アクリレート化合物とアルキレンオキシ基含有化合物との質量基準の含有比率（単官能（メタ）アクリレート化合物／アルキレンオキシ基含有化合物）は、０．０１～０．３０であることが好ましく、０．０２～０．２０であることがより好ましく、０．０５～０．２０であることがさらに好ましい。 When a monofunctional (meth) acrylate compound is used as the dispersion medium, the mass-based content ratio of the monofunctional (meth) acrylate compound and the alkyleneoxy group-containing compound (monofunctional (meth) acrylate compound / alkyleneoxy group-containing compound) is 0.01 to 0.30 is preferable, 0.02 to 0.20 is more preferable, and 0.05 to 0.20 is still more preferable.
　量子ドット蛍光体分散液に占める量子ドット蛍光体の質量基準の割合は、１質量％～１０質量％であることが好ましく、１質量％～５質量％であることがより好ましく、２質量％～４．９質量％であることがさらに好ましい。 The proportion of the quantum dot phosphor based on the mass of the quantum dot phosphor dispersion is preferably 1% by mass to 10% by mass, more preferably 1% by mass to 5% by mass, and more preferably 2% by mass to More preferably, it is 4.9% by mass.
　硬化性組成物中の量子ドット蛍光体分散液の含有率は、量子ドット蛍光体分散液に占める量子ドット蛍光体の質量基準の割合が１質量％～１０質量％である場合、硬化性組成物の全量に対して、例えば、０．５質量％～８質量％であることが好ましく、０．８質量％～５質量％であることがより好ましく、１.０質量％～４．９質量％であることがさらに好ましい。また、硬化性組成物中の量子ドット蛍光体の含有率は、硬化性組成物の全量に対して、例えば、０．０５質量％～０.８質量％であることが好ましく、０．０８質量％～０．５質量％であることがより好ましく、０．１質量％～０．４９質量％であることがさらに好ましい。量子ドット蛍光体の含有率が０．０５質量％以上であると、硬化物に励起光を照射する際に充分な発光強度が得られる傾向にあり、量子ドット蛍光体の含有率が０．８質量％以下であると、量子ドット蛍光体の凝集が抑えられる傾向にある。 The content of the quantum dot phosphor dispersion in the curable composition is such that the proportion of the quantum dot phosphor based on the mass of the quantum dot phosphor dispersion is 1% by mass to 10% by mass. For example, it is preferably 0.5% by mass to 8% by mass, more preferably 0.8% by mass to 5% by mass, and 1.0% by mass to 4.9% by mass with respect to the total amount of More preferably. Further, the content of the quantum dot phosphor in the curable composition is preferably, for example, 0.05% by mass to 0.8% by mass with respect to the total amount of the curable composition, and 0.08% by mass % To 0.5% by mass is more preferable, and 0.1% to 0.49% by mass is even more preferable. When the content of the quantum dot phosphor is 0.05% by mass or more, a sufficient emission intensity tends to be obtained when the cured product is irradiated with excitation light, and the content of the quantum dot phosphor is 0.8. When the content is less than or equal to mass%, aggregation of the quantum dot phosphor tends to be suppressed.
（アルキレンオキシ基含有化合物）
　本開示の硬化性組成物は、アルキレンオキシ基及び重合性反応基を有するアルキレンオキシ基含有化合物を含む。 (Alkyleneoxy group-containing compound)
The curable composition of the present disclosure includes an alkyleneoxy group-containing compound having an alkyleneoxy group and a polymerizable reactive group.
　アルキレンオキシ基含有化合物は、重合性反応基を２個以上有することが好ましく、重合性反応基を２個有することがより好ましい。重合性反応基を２個以上有することにより、被覆材に対する硬化物の密着性及び耐湿熱性をより向上させることができる傾向にある。
　重合性反応基としては、エチレン性二重結合を有する官能基が挙げられ、より具体的には、（メタ）アクリロイル基等が挙げられる。 The alkyleneoxy group-containing compound preferably has two or more polymerizable reactive groups, and more preferably has two polymerizable reactive groups. By having two or more polymerizable reactive groups, it tends to be possible to further improve the adhesion of the cured product to the coating material and the heat and moisture resistance.
Examples of the polymerizable reactive group include a functional group having an ethylenic double bond, and more specifically, a (meth) acryloyl group.
　アルキレンオキシ基としては、例えば、炭素数が２～４のアルキレンオキシ基が好ましく、炭素数が２又は３のアルキレンオキシ基がより好ましく、炭素数が２のアルキレンオキシ基がさらに好ましい。
　アルキレンオキシ基含有化合物は、１種のアルキレンオキシ基を有していてもよく、２種以上のアルキレンオキシ基を有していてもよい。 As the alkyleneoxy group, for example, an alkyleneoxy group having 2 to 4 carbon atoms is preferable, an alkyleneoxy group having 2 or 3 carbon atoms is more preferable, and an alkyleneoxy group having 2 carbon atoms is more preferable.
The alkyleneoxy group-containing compound may have one type of alkyleneoxy group or may have two or more types of alkyleneoxy groups.
　アルキレンオキシ基含有化合物は、複数個のアルキレンオキシ基を含むポリアルキレンオキシ基を有するポリアルキレンオキシ基含有化合物であってもよい。 The alkyleneoxy group-containing compound may be a polyalkyleneoxy group-containing compound having a polyalkyleneoxy group containing a plurality of alkyleneoxy groups.
　アルキレンオキシ基含有化合物は、２個～３０個のアルキレンオキシ基を有することが好ましく、２個～２０個のアルキレンオキシ基を有することがより好ましく、３個～１０個のアルキレンオキシ基を有することがさらに好ましく、３個～５個のアルキレンオキシ基を有することが特に好ましい。 The alkyleneoxy group-containing compound preferably has 2 to 30 alkyleneoxy groups, more preferably 2 to 20 alkyleneoxy groups, and more preferably 3 to 10 alkyleneoxy groups. Is more preferable, and it is particularly preferable to have 3 to 5 alkyleneoxy groups.
　アルキレンオキシ基含有化合物は、ビスフェノール構造を有することが好ましい。これにより、耐湿熱性により優れる傾向にある。ビスフェノール構造としては、例えば、ビスフェノールＡ構造及びビスフェノールＦ構造が挙げられ、中でも、ビスフェノールＡ構造が好ましい。 The alkyleneoxy group-containing compound preferably has a bisphenol structure. Thereby, it exists in the tendency which is more excellent in heat-and-moisture resistance. Examples of the bisphenol structure include a bisphenol A structure and a bisphenol F structure, and among them, the bisphenol A structure is preferable.
　アルキレンオキシ基含有化合物の具体例としては、ブトキシエチル（メタ）アクリレート等のアルコキシアルキル（メタ）アクリレート；ジエチレングリコールモノエチルエーテル（メタ）アクリレート、トリエチレングリコールモノブチルエーテル（メタ）アクリレート、テトラエチレングリコールモノメチルエーテル（メタ）アクリレート、ヘキサエチレングリコールモノメチルエーテル（メタ）アクリレート、オクタエチレングリコールモノメチルエーテル（メタ）アクリレート、ノナエチレングリコールモノメチルエーテル（メタ）アクリレート、ジプロピレングリコールモノメチルエーテル（メタ）アクリレート、ヘプタプロピレングリコールモノメチルエーテル（メタ）アクリレート、テトラエチレングリコールモノエチルエーテル（メタ）アクリレート等のポリアルキレングリコールモノアルキルエーテル（メタ）アクリレート；ヘキサエチレングリコールモノフェニルエーテル（メタ）アクリレート等のポリアルキレングリコールモノアリールエーテル（メタ）アクリレート；テトラヒドロフルフリル（メタ）アクリレート等の複素環を有する（メタ）アクリレート化合物；トリエチレングリコールモノ（メタ）アクリレート、テトラエチレングリコールモノ（メタ）アクリレート、ヘキサエチレングリコールモノ（メタ）アクリレート、オクタプロピレングリコールモノ（メタ）アクリレート等の水酸基を有する（メタ）アクリレート化合物；グリシジル（メタ）アクリレート等のグリシジル基を有する（メタ）アクリレート化合物；ポリエチレングリコールジ（メタ）アクリレート、ポリプロピレングリコールジ（メタ）アクリレート等のポリアルキレングリコールジ（メタ）アクリレート；エチレンオキシド付加トリメチロールプロパントリ（メタ）アクリレート等のトリ（メタ）アクリレート化合物；エチレンオキシド付加ペンタエリスリトールテトラ（メタ）アクリレート等のテトラ（メタ）アクリレート化合物；エトキシ化ビスフェノールＡジ（メタ）アクリレート、プロポキシ化ビスフェノールＡジ（メタ）アクリレート、プロポキシ化エトキシ化ビスフェノールＡジ（メタ）アクリレート等のビスフェノールジ（メタ）アクリレート化合物；などが挙げられる。
　アルキレンオキシ基含有化合物としては、中でも、エトキシ化ビスフェノールＡジ（メタ）アクリレート、プロポキシ化ビスフェノールＡジ（メタ）アクリレート及びプロポキシ化エトキシ化ビスフェノールＡジ（メタ）アクリレートが好ましく、エトキシ化ビスフェノールＡジ（メタ）アクリレートがより好ましい。
　アルキレンオキシ基含有化合物としては、１種類を単独で用いてもよく、２種類以上を併用してもよい。 Specific examples of the alkyleneoxy group-containing compound include alkoxyalkyl (meth) acrylates such as butoxyethyl (meth) acrylate; diethylene glycol monoethyl ether (meth) acrylate, triethylene glycol monobutyl ether (meth) acrylate, tetraethylene glycol monomethyl ether (Meth) acrylate, hexaethylene glycol monomethyl ether (meth) acrylate, octaethylene glycol monomethyl ether (meth) acrylate, nonaethylene glycol monomethyl ether (meth) acrylate, dipropylene glycol monomethyl ether (meth) acrylate, heptapropylene glycol monomethyl ether (Meth) acrylate, tetraethylene glycol monoethyl acetate Poly (alkylene glycol) monoalkyl ether (meth) acrylates such as ru (meth) acrylate; Polyalkylene glycol monoaryl ether (meth) acrylates such as hexaethylene glycol monophenyl ether (meth) acrylate; Tetrahydrofurfuryl (meth) acrylate etc. (Meth) acrylate compounds having a heterocyclic ring; having hydroxyl groups such as triethylene glycol mono (meth) acrylate, tetraethylene glycol mono (meth) acrylate, hexaethylene glycol mono (meth) acrylate, and octapropylene glycol mono (meth) acrylate (Meth) acrylate compounds; (meth) acrylate compounds having a glycidyl group such as glycidyl (meth) acrylate; polyethylene glycol di Poly (alkylene glycol) di (meth) acrylates such as (meth) acrylate and polypropylene glycol di (meth) acrylate; Tri (meth) acrylate compounds such as ethylene oxide-added trimethylolpropane tri (meth) acrylate; Ethylene oxide-added pentaerythritol tetra (meth) acrylate Tetra (meth) acrylate compounds such as; bisphenol di (meth) acrylate compounds such as ethoxylated bisphenol A di (meth) acrylate, propoxylated bisphenol A di (meth) acrylate, propoxylated ethoxylated bisphenol A di (meth) acrylate; Etc.
Among the alkyleneoxy group-containing compounds, ethoxylated bisphenol A di (meth) acrylate, propoxylated bisphenol A di (meth) acrylate and propoxylated ethoxylated bisphenol A di (meth) acrylate are preferred, and ethoxylated bisphenol A di ( More preferred is (meth) acrylate.
As the alkyleneoxy group-containing compound, one type may be used alone, or two or more types may be used in combination.
　硬化性組成物中のアルキレンオキシ基含有化合物の含有率は、硬化性組成物の全量に対して、例えば、３０質量％～７０質量％であることが好ましく、３５質量％～６５質量％であることが好ましく、４０質量％～６０質量％であることがさらに好ましい。アルキレンオキシ基含有化合物の含有率が３０質量％以上であると、透湿度が高くなりすぎることを抑制できる傾向にあり、アルキレンオキシ基含有化合物の含有率が７０質量％以下であると、硬化性組成物の透湿度の低下を抑制できる傾向にある。 The content of the alkyleneoxy group-containing compound in the curable composition is preferably, for example, 30% by mass to 70% by mass, and preferably 35% by mass to 65% by mass with respect to the total amount of the curable composition. It is preferably 40% by mass to 60% by mass. When the content of the alkyleneoxy group-containing compound is 30% by mass or more, moisture permeability tends to be suppressed from being excessively high. When the content of the alkyleneoxy group-containing compound is 70% by mass or less, curability is obtained. There exists a tendency which can suppress the fall of the water vapor transmission rate of a composition.
（多官能チオール化合物）
　本開示の硬化性組成物は、多官能チオール化合物を含むことが好ましい。硬化性組成物が多官能チオール化合物を含むことで、硬化性組成物が硬化する際にアルキレンオキシ基含有化合物等と多官能チオール化合物との間でエンチオール反応が進行し、硬化物の耐熱性が向上する傾向にある。また、硬化性組成物が多官能チオール化合物を含むことで、硬化物の光学特性がより向上する傾向にある。 (Polyfunctional thiol compound)
The curable composition of the present disclosure preferably includes a polyfunctional thiol compound. When the curable composition contains a polyfunctional thiol compound, the enethiol reaction proceeds between the alkyleneoxy group-containing compound and the polyfunctional thiol compound when the curable composition is cured, and the heat resistance of the cured product is increased. It tends to improve. Moreover, it exists in the tendency for the optical characteristic of hardened | cured material to improve more because a curable composition contains a polyfunctional thiol compound.
　多官能チオール化合物の具体例としては、エチレングリコールビス（３－メルカプトプロピオネート）、ジエチレングリコールビス（３－メルカプトプロピオネート）、テトラエチレングリコールビス（３－メルカプトプロピオネート）、１，２－プロピレングリコールビス（３－メルカプトプロピオネート）、ジエチレングリコールビス（３－メルカプトブチレート）、１，４－ブタンジオールビス（３－メルカプトプロピオネート）、１，４－ブタンジオールビス（３－メルカプトブチレート）、１，８－オクタンジオールビス（３－メルカプトプロピオネート）、１，８－オクタンジオールビス（３－メルカプトブチレート）、ヘキサンジオールビスチオグリコレート、トリメチロールプロパントリス（３－メルカプトプロピオネート）、トリメチロールプロパントリス（３－メルカプトブチレート）、トリメチロールプロパントリス（３－メルカプトイソブチレート）、トリメチロールプロパントリス（２－メルカプトイソブチレート）、トリメチロールプロパントリスチオグリコレート、トリス－［（３－メルカプトプロピオニルオキシ）－エチル］－イソシアヌレート、トリメチロールエタントリス（３－メルカプトブチレート）、ペンタエリスリトールテトラキス（３－メルカプトプロピオネート）、ペンタエリスリトールテトラキス（３－メルカプトブチレート）、ペンタエリスリトールテトラキス（３－メルカプトイソブチレート）、ペンタエリスリトールテトラキス（２－メルカプトイソブチレート）、ジペンタエリスリトールヘキサキス（３－メルカプトプロピオネート）、ジペンタエリスリトールヘキサキス（２－メルカプトプロピオネート）、ジペンタエリスリトールヘキサキス（３－メルカプトブチレート）、ジペンタエリスリトールヘキサキス（３－メルカプトイソブチレート）、ジペンタエリスリトールヘキサキス（２－メルカプトイソブチレート）、ペンタエリスリトールテトラキスチオグリコレート、ジペンタエリスリトールヘキサキスチオグリコレート等が挙げられる。 Specific examples of the polyfunctional thiol compound include ethylene glycol bis (3-mercaptopropionate), diethylene glycol bis (3-mercaptopropionate), tetraethylene glycol bis (3-mercaptopropionate), 1,2- Propylene glycol bis (3-mercaptopropionate), diethylene glycol bis (3-mercaptobutyrate), 1,4-butanediol bis (3-mercaptopropionate), 1,4-butanediol bis (3-mercaptobutyrate) Rate), 1,8-octanediol bis (3-mercaptopropionate), 1,8-octanediol bis (3-mercaptobutyrate), hexanediol bisthioglycolate, trimethylolpropane tris (3-mercaptopropiate) Onee ), Trimethylolpropane tris (3-mercaptobutyrate), trimethylolpropane tris (3-mercaptoisobutyrate), trimethylolpropane tris (2-mercaptoisobutyrate), trimethylolpropane tristhioglycolate, tris- [(3-mercaptopropionyloxy) -ethyl] -isocyanurate, trimethylolethane tris (3-mercaptobutyrate), pentaerythritol tetrakis (3-mercaptopropionate), pentaerythritol tetrakis (3-mercaptobutyrate), Pentaerythritol tetrakis (3-mercaptoisobutyrate), pentaerythritol tetrakis (2-mercaptoisobutyrate), dipentaerythritol hexakis (3-mercapto) Lopionate), dipentaerythritol hexakis (2-mercaptopropionate), dipentaerythritol hexakis (3-mercaptobutyrate), dipentaerythritol hexakis (3-mercaptoisobutyrate), dipentaerythritol hexakis ( 2-mercaptoisobutyrate), pentaerythritol tetrakisthioglycolate, dipentaerythritol hexakisthioglycolate and the like.
　本開示の硬化性組成物は、１分子中に１個のチオール基を有する単官能チオール化合物を含んでいてもよい。 The curable composition of the present disclosure may contain a monofunctional thiol compound having one thiol group in one molecule.
　単官能チオール化合物の具体例としては、ヘキサンチオール、１－ヘプタンチオール、１－オクタンチオール、１－ノナンチオール、１－デカンチオール、３－メルカプトプロピオン酸、メルカプトプロピオン酸メチル、メルカプトプロピオン酸メトキシブチル、メルカプトプロピオン酸オクチル、メルカプトプロピオン酸トリデシル、２－エチルヘキシル－３－メルカプトプロピオネート、ｎ－オクチル－３－メルカプトプロピオネート等が挙げられる。 Specific examples of monofunctional thiol compounds include hexanethiol, 1-heptanethiol, 1-octanethiol, 1-nonanethiol, 1-decanethiol, 3-mercaptopropionic acid, methyl mercaptopropionate, methoxybutyl mercaptopropionate, Examples include octyl mercaptopropionate, tridecyl mercaptopropionate, 2-ethylhexyl-3-mercaptopropionate, n-octyl-3-mercaptopropionate, and the like.
　硬化性組成物がチオール化合物を含む場合、硬化性組成物中のチオール化合物（多官能チオール化合物及び必要に応じて用いられる単官能チオール化合物の合計、好ましくは多官能チオール化合物）の含有率は、硬化性組成物の全量に対して、例えば、１５質量％～７０質量％であることが好ましく、２０質量％～６５質量％であることがより好ましく、２５質量％～６０質量％であることがさらに好ましく、３０質量％～５０質量％であることが特に好ましい。チオール化合物の含有率が１５質量％以上であることにより、硬化性組成物の透湿度の低下を抑制できる傾向にある。チオール化合物の含有率が７０質量％以下であることにより、透湿度が高くなりすぎることを抑制できる傾向にある。 When the curable composition contains a thiol compound, the content of the thiol compound in the curable composition (the sum of the polyfunctional thiol compound and the monofunctional thiol compound used as necessary, preferably the polyfunctional thiol compound) is: For example, the content is preferably 15% by mass to 70% by mass, more preferably 20% by mass to 65% by mass, and more preferably 25% by mass to 60% by mass with respect to the total amount of the curable composition. More preferably, the content is 30% by mass to 50% by mass. It exists in the tendency which can suppress the fall of the water vapor transmission rate of a curable composition because the content rate of a thiol compound is 15 mass% or more. When the content of the thiol compound is 70% by mass or less, the moisture permeability tends to be suppressed from becoming too high.
　多官能チオール化合物及び必要に応じて用いられる単官能チオール化合物の合計に占める多官能チオール化合物の質量基準の割合は、６０質量％～１００質量％であることが好ましく、７０質量％～１００質量％であることがより好ましく、８０質量％～１００質量％であることがさらに好ましい。 The proportion of the polyfunctional thiol compound based on the mass of the polyfunctional thiol compound and the monofunctional thiol compound used as necessary is preferably 60% by mass to 100% by mass, and more preferably 70% by mass to 100% by mass. More preferably, it is more preferably 80% by mass to 100% by mass.
　アルキレンオキシ基含有化合物中の重合性反応基の数に対するチオール化合物（多官能チオール化合物及び必要に応じて用いられる単官能チオール化合物の合計、好ましくは多官能チオール化合物）中のチオール基の数の比率（チオール基の数／重合性反応基の数）は、０．５～５．０であることが好ましく、０．８～４．０であることがより好ましく、１．０～３．５であることがさらに好ましく、１．２～３．０であることが特に好ましい。 Ratio of the number of thiol groups in the thiol compound (the sum of the polyfunctional thiol compound and the monofunctional thiol compound used as necessary, preferably the polyfunctional thiol compound) to the number of polymerizable reactive groups in the alkyleneoxy group-containing compound (Number of thiol groups / number of polymerizable reactive groups) is preferably 0.5 to 5.0, more preferably 0.8 to 4.0, and 1.0 to 3.5. More preferably, it is particularly preferably 1.2 to 3.0.
（光重合開始剤）
　本開示の硬化性組成物は、光重合開始剤を含む。光重合開始剤としては特に制限されず、具体例として、紫外線等の活性エネルギー線の照射によりラジカルを発生する化合物が挙げられる。 (Photopolymerization initiator)
The curable composition of the present disclosure includes a photopolymerization initiator. The photopolymerization initiator is not particularly limited, and specific examples include compounds that generate radicals upon irradiation with active energy rays such as ultraviolet rays.
　光重合開始剤の具体例としては、ベンゾフェノン、Ｎ，Ｎ’－テトラアルキル－４，４’－ジアミノベンゾフェノン、２－ベンジル－２－ジメチルアミノ－１－（４－モルホリノフェニル）－ブタノン－１、２－メチル－１－［４－（メチルチオ）フェニル］－２－モルホリノ－プロパノン－１、４，４’－ビス（ジメチルアミノ）ベンゾフェノン（「ミヒラーケトン」とも称される）、４，４’－ビス（ジエチルアミノ）ベンゾフェノン、４－メトキシ－４’－ジメチルアミノベンゾフェノン、１－ヒドロキシシクロヘキシルフェニルケトン、１－（４－イソプロピルフェニル）－２－ヒドロキシ－２－メチルプロパン－１－オン、１－（４－（２－ヒドロキシエトキシ）－フェニル）－２－ヒドロキシ－２－メチル－１－プロパン－１－オン、２－ヒドロキシ－２－メチル－１－フェニルプロパン－１－オン等の芳香族ケトン化合物；アルキルアントラキノン、フェナントレンキノン等のキノン化合物；ベンゾイン、アルキルベンゾイン等のベンゾイン化合物；ベンゾインアルキルエーテル、ベンゾインフェニルエーテル等のベンゾインエーテル化合物；ベンジルジメチルケタール等のベンジル誘導体；２－（ｏ－クロロフェニル）－４，５－ジフェニルイミダゾール二量体、２－（ｏ－クロロフェニル）－４，５－ジ（ｍ－メトキシフェニル）イミダゾール二量体、２－（ｏ－フルオロフェニル）－４，５－ジフェニルイミダゾール二量体、２－（ｏ－メトキシフェニル）－４，５－ジフェニルイミダゾール二量体、２，４－ジ（ｐ－メトキシフェニル）－５－フェニルイミダゾール二量体、２－（２，４－ジメトキシフェニル）－４，５－ジフェニルイミダゾール二量体等の２，４，５－トリアリールイミダゾール二量体；９－フェニルアクリジン、１，７－（９，９’－アクリジニル）ヘプタン等のアクリジン誘導体；１，２－オクタンジオン１－［４－（フェニルチオ）－２－（Ｏ－ベンゾイルオキシム）］、エタノン１－［９－エチル－６－（２－メチルベンゾイル）－９Ｈ－カルバゾール－３－イル］－１－（Ｏ－アセチルオキシム）等のオキシムエステル化合物；７－ジエチルアミノ－４－メチルクマリン等のクマリン化合物；２，４－ジエチルチオキサントン等のチオキサントン化合物；２，４，６－トリメチルベンゾイル－ジフェニル－ホスフィンオキサイド、２，４，６－トリメチルベンゾイル－フェニル－エトキシ－ホスフィンオキサイド等のアシルホスフィンオキサイド化合物；などが挙げられる。硬化性組成物は、１種類の光重合開始剤を単独で含んでいてもよく、２種類以上の光重合開始剤を組み合わせて含んでいてもよい。 Specific examples of the photopolymerization initiator include benzophenone, N, N′-tetraalkyl-4,4′-diaminobenzophenone, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1, 2-methyl-1- [4- (methylthio) phenyl] -2-morpholino-propanone-1,4,4′-bis (dimethylamino) benzophenone (also referred to as “Michler ketone”), 4,4′-bis (Diethylamino) benzophenone, 4-methoxy-4′-dimethylaminobenzophenone, 1-hydroxycyclohexyl phenyl ketone, 1- (4-isopropylphenyl) -2-hydroxy-2-methylpropan-1-one, 1- (4- (2-hydroxyethoxy) -phenyl) -2-hydroxy-2-methyl-1-propane-1 Aromatic ketone compounds such as ON and 2-hydroxy-2-methyl-1-phenylpropan-1-one; quinone compounds such as alkylanthraquinone and phenanthrenequinone; benzoin compounds such as benzoin and alkylbenzoin; benzoin alkyl ether and benzoin phenyl Benzoin ether compounds such as ether; benzyl derivatives such as benzyldimethyl ketal; 2- (o-chlorophenyl) -4,5-diphenylimidazole dimer, 2- (o-chlorophenyl) -4,5-di (m-methoxy) Phenyl) imidazole dimer, 2- (o-fluorophenyl) -4,5-diphenylimidazole dimer, 2- (o-methoxyphenyl) -4,5-diphenylimidazole dimer, 2,4-di (P-methoxyphenyl) -5-phenyl 2,4,5-triarylimidazole dimers such as dazole dimer, 2- (2,4-dimethoxyphenyl) -4,5-diphenylimidazole dimer; 9-phenylacridine, 1,7- ( Acridine derivatives such as 9,9′-acridinyl) heptane; 1,2-octanedione 1- [4- (phenylthio) -2- (O-benzoyloxime)], ethanone 1- [9-ethyl-6- (2 Oxime ester compounds such as -methylbenzoyl) -9H-carbazol-3-yl] -1- (O-acetyloxime); coumarin compounds such as 7-diethylamino-4-methylcoumarin; thioxanthones such as 2,4-diethylthioxanthone Compound; 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, 2,4,6-trimethylbenzoyl -Acylphosphine oxide compounds such as phenyl-ethoxy-phosphine oxide; The curable composition may contain one kind of photopolymerization initiator alone, or may contain two or more kinds of photopolymerization initiators in combination.
　光重合開始剤としては、硬化性の観点から、アシルホスフィンオキサイド化合物、芳香族ケトン化合物、及びオキシムエステル化合物からなる群より選択される少なくとも１種が好ましく、アシルホスフィンオキサイド化合物及び芳香族ケトン化合物からなる群より選択される少なくとも１種がより好ましく、アシルホスフィンオキサイド化合物がさらに好ましい。 The photopolymerization initiator is preferably at least one selected from the group consisting of an acylphosphine oxide compound, an aromatic ketone compound, and an oxime ester compound from the viewpoint of curability, and includes an acylphosphine oxide compound and an aromatic ketone compound. More preferably, at least one selected from the group consisting of acylphosphine oxide compounds is more preferable.
　硬化性組成物中の光重合開始剤の含有率は、硬化性組成物の全量に対して、例えば、０．１質量％～５質量％であることが好ましく、０．１質量％～３質量％であることがより好ましく、０．３質量％～１．５質量％であることがさらに好ましい。光重合開始剤の含有率が０．１質量％以上であると、硬化性組成物の感度が充分なものとなる傾向にあり、光重合開始剤の含有率が５質量％以下であると、硬化性組成物の色相への影響及び保存安定性の低下が抑えられる傾向にある。 The content of the photopolymerization initiator in the curable composition is preferably, for example, 0.1% by mass to 5% by mass, and preferably 0.1% by mass to 3% by mass with respect to the total amount of the curable composition. %, More preferably 0.3% by mass to 1.5% by mass. When the content of the photopolymerization initiator is 0.1% by mass or more, the sensitivity of the curable composition tends to be sufficient, and when the content of the photopolymerization initiator is 5% by mass or less, There exists a tendency for the influence on the hue of a curable composition and the fall of storage stability to be suppressed.
（液状媒体）
　本開示の硬化性組成物は、液状媒体を含んでいてもよい。液状媒体とは、室温（２５℃）において液体の状態の媒体をいう。 (Liquid medium)
The curable composition of the present disclosure may include a liquid medium. A liquid medium means a medium in a liquid state at room temperature (25 ° C.).
　液状媒体の具体例としては、アセトン、メチルエチルケトン、メチル－ｎ－プロピルケトン、メチルイソプロピルケトン、メチル－ｎ－ブチルケトン、メチルイソブチルケトン、メチル－ｎ－ペンチルケトン、メチル－ｎ－ヘキシルケトン、ジエチルケトン、ジプロピルケトン、ジイソブチルケトン、トリメチルノナノン、シクロヘキサノン、シクロペンタノン、メチルシクロヘキサノン、２，４－ペンタンジオン、アセトニルアセトン等のケトン溶剤；ジエチルエーテル、メチルエチルエーテル、メチル－ｎ－プロピルエーテル、ジイソプロピルエーテル、テトラヒドロフラン、メチルテトラヒドロフラン、ジオキサン、ジメチルジオキサン、エチレングリコールジメチルエーテル、エチレングリコールジエチルエーテル、エチレングリコールジ－ｎ－プロピルエーテル、エチレングリコールジ－ｎ－ブチルエーテル、ジエチレングリコールジメチルエーテル、ジエチレングリコールジエチルエーテル、ジエチレングリコールメチルエチルエーテル、ジエチレングリコールメチル－ｎ－プロピルエーテル、ジエチレングリコールメチル－ｎ－ブチルエーテル、ジエチレングリコールジ－ｎ－プロピルエーテル、ジエチレングリコールジ－ｎ－ブチルエーテル、ジエチレングリコールメチル－ｎ－ヘキシルエーテル、トリエチレングリコールジメチルエーテル、トリエチレングリコールジエチルエーテル、トリエチレングリコールメチルエチルエーテル、トリエチレングリコールメチル－ｎ－ブチルエーテル、トリエチレングリコールジ－ｎ－ブチルエーテル、トリエチレングリコールメチル－ｎ－ヘキシルエーテル、テトラエチレングリコールジメチルエーテル、テトラエチレングリコールジエチルエーテル、テトラエチレングリコールメチルエチルエーテル、テトラエチレングリコールメチル－ｎ－ブチルエーテル、テトラエチレングリコールジ－ｎ－ブチルエーテル、テトラエチレングリコールメチル－ｎ－ヘキシルエーテル、プロピレングリコールジメチルエーテル、プロピレングリコールジエチルエーテル、プロピレングリコールジ－ｎ－プロピルエーテル、プロピレングリコールジ－ｎ－ブチルエーテル、ジプロピレングリコールジメチルエーテル、ジプロピレングリコールジエチルエーテル、ジプロピレングリコールメチルエチルエーテル、ジプロピレングリコールメチル－ｎ－ブチルエーテル、ジプロピレングリコールジ－ｎ－プロピルエーテル、ジプロピレングリコールジ－ｎ－ブチルエーテル、ジプロピレングリコールメチル－ｎ－ヘキシルエーテル、トリプロピレングリコールジメチルエーテル、トリプロピレングリコールジエチルエーテル、トリプロピレングリコールメチルエチルエーテル、トリプロピレングリコールメチル－ｎ－ブチルエーテル、トリプロピレングリコールジ－ｎ－ブチルエーテル、トリプロピレングリコールメチル－ｎ－ヘキシルエーテル、テトラプロピレングリコールジメチルエーテル、テトラプロピレングリコールジエチルエーテル、テトラプロピレングリコールメチルエチルエーテル、テトラプロピレングリコールメチル－ｎ－ブチルエーテル、テトラプロピレングリコールジ－ｎ－ブチルエーテル、テトラプロピレングリコールメチル－ｎ－ヘキシルエーテル等のエーテル溶剤；プロピレンカーボネート、エチレンカーボネート、ジエチルカーボネート等のカーボネート溶剤；酢酸メチル、酢酸エチル、酢酸ｎ－プロピル、酢酸イソプロピル、酢酸ｎ－ブチル、酢酸イソブチル、酢酸ｓｅｃ－ブチル、酢酸ｎ－ペンチル、酢酸ｓｅｃ－ペンチル、酢酸３－メトキシブチル、酢酸メチルペンチル、酢酸２－エチルブチル、酢酸２－エチルヘキシル、酢酸２－（２－ブトキシエトキシ）エチル、酢酸ベンジル、酢酸シクロヘキシル、酢酸メチルシクロヘキシル、酢酸ノニル、アセト酢酸メチル、アセト酢酸エチル、酢酸ジエチレングリコールメチルエーテル、酢酸ジエチレングリコールモノエチルエーテル、酢酸ジプロピレングリコールメチルエーテル、酢酸ジプロピレングリコールエチルエーテル、ジ酢酸グリコール、酢酸メトキシトリエチレングリコール、プロピオン酸エチル、プロピオン酸ｎ－ブチル、プロピオン酸イソアミル、シュウ酸ジエチル、シュウ酸ジ－ｎ－ブチル、乳酸メチル、乳酸エチル、乳酸ｎ－ブチル、乳酸ｎ－アミル、エチレングリコールメチルエーテルプロピオネート、エチレングリコールエチルエーテルプロピオネート、エチレングリコールメチルエーテルアセテート、エチレングリコールエチルエーテルアセテート、プロピレングリコールメチルエーテルアセテート、プロピレングリコールエチルエーテルアセテート、プロピレングリコールプロピルエーテルアセテート、γ－ブチロラクトン、γ－バレロラクトン等のエステル溶剤；アセトニトリル、Ｎ－メチルピロリジノン、Ｎ－エチルピロリジノン、Ｎ－プロピルピロリジノン、Ｎ－ブチルピロリジノン、Ｎ－ヘキシルピロリジノン、Ｎ－シクロヘキシルピロリジノン、Ｎ，Ｎ－ジメチルホルムアミド、Ｎ，Ｎ－ジメチルアセトアミド、ジメチルスルホキシド等の非プロトン性極性溶剤；メタノール、エタノール、ｎ－プロパノール、イソプロパノール、ｎ－ブタノール、イソブタノール、ｓｅｃ－ブタノール、ｔ－ブタノール、ｎ－ペンタノール、イソペンタノール、２－メチルブタノール、ｓｅｃ－ペンタノール、ｔ－ペンタノール、３－メトキシブタノール、ｎ－ヘキサノール、２－メチルペンタノール、ｓｅｃ－ヘキサノール、２－エチルブタノール、ｓｅｃ－ヘプタノール、ｎ－オクタノール、２－エチルヘキサノール、ｓｅｃ－オクタノール、ｎ－ノニルアルコール、ｎ－デカノール、ｓｅｃ－ウンデシルアルコール、トリメチルノニルアルコール、ｓｅｃ－テトラデシルアルコール、ｓｅｃ－ヘプタデシルアルコール、シクロヘキサノール、メチルシクロヘキサノール、ベンジルアルコール、エチレングリコール、１，２－プロピレングリコール、１，３－ブチレングリコール、ジエチレングリコール、ジプロピレングリコール、トリエチレングリコール、トリプロピレングリコール等のアルコール溶剤；エチレングリコールモノメチルエーテル、エチレングリコールモノエチルエーテル、エチレングリコールモノフェニルエーテル、ジエチレングリコールモノメチルエーテル、ジエチレングリコールモノエチルエーテル、ジエチレングリコールモノ－ｎ－ブチルエーテル、ジエチレングリコールモノ－ｎ－ヘキシルエーテル、トリエチレングリコールモノエチルエーテル、テトラエチレングリコールモノ－ｎ－ブチルエーテル、プロピレングリコールモノメチルエーテル、ジプロピレングリコールモノメチルエーテル、ジプロピレングリコールモノエチルエーテル、トリプロピレングリコールモノメチルエーテル等のグリコールモノエーテル溶剤；テルピネン、テルピネオール、ミルセン、アロオシメン、リモネン、ジペンテン、ピネン、カルボン、オシメン、フェランドレン等のテルペン溶剤；ジメチルシリコーンオイル、メチルフェニルシリコーンオイル、メチルハイドロジェンシリコーンオイル等のストレートシリコーンオイル；アミノ変性シリコーンオイル、エポキシ変性シリコーンオイル、カルボキシ変性シリコーンオイル、カルビノール変性シリコーンオイル、メルカプト変性シリコーンオイル、異種官能基変性シリコーンオイル、ポリエーテル変性シリコーンオイル、メチルスチリル変性シリコーンオイル、親水性特殊変性シリコーンオイル、高級アルコキシ変性シリコーンオイル、高級脂肪酸変性シリコーンオイル、フッ素変性シリコーンオイル等の変性シリコーンオイル；ブタン酸、ペンタン酸、ヘキサン酸、ヘプタン酸、オクタン酸、ノナン酸、デカン酸、ウンデカン酸、ドデカン酸、トリデカン酸、テトラデカン酸、ペンタデカン酸、ヘキサデカン酸、ヘプタデカン酸、オクタデカン酸、ノナデカン酸、イコサン酸、エイコセン酸等の炭素数４以上の飽和脂肪族モノカルボン酸；オレイン酸、エライジン酸、リノール酸、パルミトレイン酸等の炭素数８以上の不飽和脂肪族モノカルボン酸；などが挙げられる。硬化性組成物が液状媒体を含む場合、１種類の液状媒体を単独で含んでいてもよく、２種類以上の液状媒体を組み合わせて含んでいてもよい。 Specific examples of the liquid medium include acetone, methyl ethyl ketone, methyl-n-propyl ketone, methyl isopropyl ketone, methyl-n-butyl ketone, methyl isobutyl ketone, methyl-n-pentyl ketone, methyl-n-hexyl ketone, diethyl ketone, Ketone solvents such as dipropyl ketone, diisobutyl ketone, trimethylnonanone, cyclohexanone, cyclopentanone, methylcyclohexanone, 2,4-pentanedione, acetonylacetone; diethyl ether, methyl ethyl ether, methyl-n-propyl ether, diisopropyl Ether, tetrahydrofuran, methyltetrahydrofuran, dioxane, dimethyldioxane, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol Di-n-propyl ether, ethylene glycol di-n-butyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol methyl ethyl ether, diethylene glycol methyl n-propyl ether, diethylene glycol methyl n-butyl ether, diethylene glycol di-n-propyl ether, Diethylene glycol di-n-butyl ether, diethylene glycol methyl-n-hexyl ether, triethylene glycol dimethyl ether, triethylene glycol diethyl ether, triethylene glycol methyl ethyl ether, triethylene glycol methyl n-butyl ether, triethylene glycol di-n-butyl ether , Triethylene glycol Methyl-n-hexyl ether, tetraethylene glycol dimethyl ether, tetraethylene glycol diethyl ether, tetraethylene glycol methyl ethyl ether, tetraethylene glycol methyl n-butyl ether, tetraethylene glycol di-n-butyl ether, tetraethylene glycol methyl n- Hexyl ether, propylene glycol dimethyl ether, propylene glycol diethyl ether, propylene glycol di-n-propyl ether, propylene glycol di-n-butyl ether, dipropylene glycol dimethyl ether, dipropylene glycol diethyl ether, dipropylene glycol methyl ethyl ether, dipropylene glycol Methyl-n-butyl ether, dipropy Lenglycol di-n-propyl ether, dipropylene glycol di-n-butyl ether, dipropylene glycol methyl-n-hexyl ether, tripropylene glycol dimethyl ether, tripropylene glycol diethyl ether, tripropylene glycol methyl ethyl ether, tripropylene glycol methyl -N-butyl ether, tripropylene glycol di-n-butyl ether, tripropylene glycol methyl-n-hexyl ether, tetrapropylene glycol dimethyl ether, tetrapropylene glycol diethyl ether, tetrapropylene glycol methyl ethyl ether, tetrapropylene glycol methyl-n-butyl ether Tetrapropylene glycol di-n-butyl ether, Tet Ether solvents such as propylene glycol methyl-n-hexyl ether; carbonate solvents such as propylene carbonate, ethylene carbonate, diethyl carbonate; methyl acetate, ethyl acetate, n-propyl acetate, isopropyl acetate, n-butyl acetate, isobutyl acetate, sec -Butyl, n-pentyl acetate, sec-pentyl acetate, 3-methoxybutyl acetate, methyl pentyl acetate, 2-ethylbutyl acetate, 2-ethylhexyl acetate, 2- (2-butoxyethoxy) ethyl acetate, benzyl acetate, cyclohexyl acetate, Methyl cyclohexyl acetate, nonyl acetate, methyl acetoacetate, ethyl acetoacetate, diethylene glycol methyl ether acetate, diethylene glycol monoethyl ether acetate, dipropylene glycol methyl acetate Dipropylene glycol ethyl ether, diacetic acid ethyl acetate, diacetic acid glycol, methoxytriethylene glycol acetate, ethyl propionate, n-butyl propionate, isoamyl propionate, diethyl oxalate, di-n-butyl oxalate, methyl lactate, ethyl lactate , N-butyl lactate, n-amyl lactate, ethylene glycol methyl ether propionate, ethylene glycol ethyl ether propionate, ethylene glycol methyl ether acetate, ethylene glycol ethyl ether acetate, propylene glycol methyl ether acetate, propylene glycol ethyl ether acetate , Ester solvents such as propylene glycol propyl ether acetate, γ-butyrolactone, γ-valerolactone; acetonitrile, N- Aprotic polarities such as tilpyrrolidinone, N-ethylpyrrolidinone, N-propylpyrrolidinone, N-butylpyrrolidinone, N-hexylpyrrolidinone, N-cyclohexylpyrrolidinone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethylsulfoxide Solvent: methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol, t-butanol, n-pentanol, isopentanol, 2-methylbutanol, sec-pentanol, t-pentanol , 3-methoxybutanol, n-hexanol, 2-methylpentanol, sec-hexanol, 2-ethylbutanol, sec-heptanol, n-octanol, 2-ethylhexanol, sec-o Octanol, n-nonyl alcohol, n-decanol, sec-undecyl alcohol, trimethylnonyl alcohol, sec-tetradecyl alcohol, sec-heptadecyl alcohol, cyclohexanol, methylcyclohexanol, benzyl alcohol, ethylene glycol, 1,2- Alcohol solvents such as propylene glycol, 1,3-butylene glycol, diethylene glycol, dipropylene glycol, triethylene glycol, tripropylene glycol; ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monophenyl ether, diethylene glycol monomethyl ether, diethylene glycol Monoethyl ether, diethylene glycol mono-n-butyl ether Diethylene glycol mono-n-hexyl ether, triethylene glycol monoethyl ether, tetraethylene glycol mono-n-butyl ether, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether, tripropylene glycol monomethyl ether, etc. Glycol monoether solvents; Terpene solvents such as terpinene, terpineol, myrcene, alloocimene, limonene, dipentene, pinene, carvone, oximene, and ferrandylene; straight silicone oils such as dimethyl silicone oil, methylphenyl silicone oil, and methylhydrogen silicone oil Amino-modified silicone oil, epoxy-modified silicone oil, cal Xyoxy-modified silicone oil, carbinol-modified silicone oil, mercapto-modified silicone oil, heterogeneous functional group-modified silicone oil, polyether-modified silicone oil, methylstyryl-modified silicone oil, hydrophilic specially-modified silicone oil, higher alkoxy-modified silicone oil, higher fatty acid Modified silicone oil such as modified silicone oil and fluorine-modified silicone oil; butanoic acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid, tridecanoic acid, tetradecanoic acid, pentadecanoic acid, Saturated aliphatic monocarboxylic acids having 4 or more carbon atoms such as hexadecanoic acid, heptadecanoic acid, octadecanoic acid, nonadecanoic acid, icosanoic acid, eicosenoic acid; oleic acid, elaidic acid, linoleic acid, And unsaturated aliphatic monocarboxylic acids having 8 or more carbon atoms such as lumitoleic acid. When the curable composition contains a liquid medium, one kind of liquid medium may be contained alone, or two or more kinds of liquid media may be contained in combination.
　硬化性組成物が液状媒体を含む場合、硬化性組成物中の液状媒体の含有率は、硬化性組成物の全量に対して、例えば、１質量％～１０質量％であることが好ましく、４質量％～１０質量％であることがより好ましく、４質量％～７質量％であることがさらに好ましい。 When the curable composition contains a liquid medium, the content of the liquid medium in the curable composition is preferably, for example, 1% by mass to 10% by mass with respect to the total amount of the curable composition. The content is more preferably 10% by mass to 10% by mass, and further preferably 4% by mass to 7% by mass.
（炭素数１～１７であるカルボン酸）
　本開示の硬化性組成物は、炭素数１～１７であるカルボン酸（以下、「特定カルボン酸」とも称する）を含んでいてもよい。特定カルボン酸は、硬化物表面にしみでにくく、硬化物の信頼性に優れる観点、及び立体障害が少なく、量子ドット蛍光体に配位しやすくなる観点から、炭素数２～１２であるカルボン酸が好ましく、炭素数２～１０であるカルボン酸がより好ましく、炭素数３～８であるカルボン酸がさらに好ましく、炭素数３～６であるカルボン酸が特に好ましく、炭素数３～５であるカルボン酸がより一層好ましい。
　なお、カルボキシ基の炭素は、特定カルボン酸中の炭素数に含めるものとする。 (Carboxylic acid having 1 to 17 carbon atoms)
The curable composition of the present disclosure may contain a carboxylic acid having 1 to 17 carbon atoms (hereinafter also referred to as “specific carboxylic acid”). The specific carboxylic acid is a carboxylic acid having 2 to 12 carbon atoms from the viewpoint of being hard to be stained on the surface of the cured product, excellent in reliability of the cured product, and having less steric hindrance and being easily coordinated to the quantum dot phosphor. The carboxylic acid having 2 to 10 carbon atoms is more preferable, the carboxylic acid having 3 to 8 carbon atoms is more preferable, the carboxylic acid having 3 to 6 carbon atoms is particularly preferable, and the carboxylic acid having 3 to 5 carbon atoms is more preferable. Acid is even more preferred.
In addition, carbon of a carboxy group shall be included in the carbon number in specific carboxylic acid.
　特定カルボン酸としては、不飽和カルボン酸であってもよく、飽和カルボン酸であってもよい。例えば、不飽和カルボン酸中の炭素炭素二重結合が多官能チオール化合物中のチオール基と反応することにより、硬化物表面に特定カルボン酸がしみでにくくなり、硬化物の信頼性に優れる観点から、不飽和カルボン酸が好ましく、メタクリル酸、アクリル酸等がより好ましい。 The specific carboxylic acid may be an unsaturated carboxylic acid or a saturated carboxylic acid. For example, the carbon-carbon double bond in the unsaturated carboxylic acid reacts with the thiol group in the polyfunctional thiol compound, so that the specific carboxylic acid is less likely to be stained on the surface of the cured product, and from the viewpoint of excellent reliability of the cured product. Unsaturated carboxylic acid is preferable, and methacrylic acid, acrylic acid and the like are more preferable.
　特定カルボン酸としては、カルボキシ基を１つ以上有するカルボン酸であってもよく、カルボキシ基を２つ以上有するカルボン酸であってもよい。 The specific carboxylic acid may be a carboxylic acid having one or more carboxy groups, or a carboxylic acid having two or more carboxy groups.
　特定カルボン酸は、置換基を有していてもよい。置換基として、具体的には、チオール基、アミノ基、ヒドロキシ基、アルコキシ基、アシル基、スルホン酸基、アリール基、ハロゲン原子、メタクリル基、アクリル基等が挙げられる。特定カルボン酸における炭素数には、置換基中の炭素が含まれないものとする。 The specific carboxylic acid may have a substituent. Specific examples of the substituent include a thiol group, amino group, hydroxy group, alkoxy group, acyl group, sulfonic acid group, aryl group, halogen atom, methacryl group and acrylic group. The number of carbon atoms in the specific carboxylic acid does not include carbon in the substituent.
　特定カルボン酸としては、具体的には、蟻酸、酢酸、プロピオン酸、酪酸、イソ酪酸、吉草酸、イソ吉草酸、カプロン酸、２－エチル酪酸、エナント酸、カプリル酸、ペラルゴン酸、カプリン酸、ラウリン酸、ミスチリン酸、パルミチン酸、マルガリン酸、メタクリル酸、アクリル酸、フマル酸、マレイン酸、メルカプト酢酸、メルカプトプロピオン酸、メルカプト酪酸、メルカプト吉草酸、乳酸、リンゴ酸、クエン酸、安息香酸、フェニル酢酸、フェニルプロピオン酸、フタル酸、イソフタル酸、テレフタル酸、サリチル酸、ε－アミノカプロン酸等が挙げられる。中でも、特定カルボン酸としては、酢酸、メルカプトプロピオン酸及びメタクリル酸からなる群から選ばれる少なくとも１つを含むことが好ましい。
　特定カルボン酸としては、１種類を単独で用いてもよく、２種類以上を併用してもよい。 Specific examples of the carboxylic acid include formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, caproic acid, 2-ethylbutyric acid, enanthic acid, caprylic acid, pelargonic acid, capric acid, Lauric acid, mytilic acid, palmitic acid, margaric acid, methacrylic acid, acrylic acid, fumaric acid, maleic acid, mercaptoacetic acid, mercaptopropionic acid, mercaptobutyric acid, mercaptovaleric acid, lactic acid, malic acid, citric acid, benzoic acid, phenyl Examples include acetic acid, phenylpropionic acid, phthalic acid, isophthalic acid, terephthalic acid, salicylic acid, and ε-aminocaproic acid. Among these, the specific carboxylic acid preferably includes at least one selected from the group consisting of acetic acid, mercaptopropionic acid, and methacrylic acid.
As the specific carboxylic acid, one type may be used alone, or two or more types may be used in combination.
　また、硬化性組成物が特定カルボン酸を含む場合、量子ドット蛍光体に対する特定カルボン酸の質量基準での含有比率（特定カルボン酸／量子ドット蛍光体）は、硬化物の信頼性及び量子ドット蛍光体への配位性の観点から、０．０６～６．２であることが好ましく、０．０８～５．５であることがより好ましく、０．０９～５．３であることがさらに好ましい。 In addition, when the curable composition contains a specific carboxylic acid, the content ratio (specific carboxylic acid / quantum dot phosphor) of the specific carboxylic acid with respect to the quantum dot phosphor on the mass basis determines the reliability of the cured product and the quantum dot fluorescence. From the viewpoint of coordination to the body, it is preferably 0.06 to 6.2, more preferably 0.08 to 5.5, and still more preferably 0.09 to 5.3. .
　また、本開示の硬化性組成物は、オレイン酸等の炭素数１８以上のカルボン酸を含んでいてもよく、含んでいなくてもよい。 The curable composition of the present disclosure may or may not contain a carboxylic acid having 18 or more carbon atoms such as oleic acid.
（白色顔料）
　本開示の硬化性組成物は、白色顔料を含んでいてもよい。
　白色顔料の具体例としては、酸化チタン、硫酸バリウム、酸化亜鉛、炭酸カルシウム等が挙げられる。これらの中でも、光散乱効率の観点から酸化チタンであることが好ましい。
　硬化性組成物が白色顔料として酸化チタンを含む場合、酸化チタンとしては、ルチル型酸化チタンであってもアナターゼ型酸化チタンであってもよく、ルチル型酸化チタンであることが好ましい。 (White pigment)
The curable composition of the present disclosure may contain a white pigment.
Specific examples of the white pigment include titanium oxide, barium sulfate, zinc oxide, calcium carbonate and the like. Among these, titanium oxide is preferable from the viewpoint of light scattering efficiency.
When the curable composition contains titanium oxide as a white pigment, the titanium oxide may be rutile titanium oxide or anatase titanium oxide, and is preferably rutile titanium oxide.
　白色顔料の平均粒子径は、０．１μｍ～１μｍであることが好ましく、０．２μｍ～０．８μｍであることがより好ましく、０．２μｍ～０．５μｍであることがさらに好ましい。
　本開示において白色顔料の平均粒子径は、以下のようにして測定することができる。
　硬化性組成物から抽出した白色顔料を、界面活性剤を含んだ精製水に分散させ、分散液を得る。この分散液を用いてレーザー回折式粒度分布測定装置（例えば、株式会社島津製作所、ＳＡＬＤ－３０００Ｊ）で測定される体積基準の粒度分布において、小径側からの積算が５０％となるときの値（メジアン径（Ｄ５０））を白色顔料の平均粒子径とする。硬化性組成物から白色顔料を抽出する方法としては、例えば、硬化性組成物を液状媒体で希釈し、遠心分離処理等により白色顔料を沈澱させて分収することで得ることができる。
　なお、硬化物中に含まれる白色顔料の平均粒子径は、走査型電子顕微鏡を用いた粒子の観察により、５０個の粒子について円相当径（長径と短径の幾何平均）を算出し、その算術平均値として求めることができる。 The average particle diameter of the white pigment is preferably 0.1 μm to 1 μm, more preferably 0.2 μm to 0.8 μm, and further preferably 0.2 μm to 0.5 μm.
In the present disclosure, the average particle size of the white pigment can be measured as follows.
The white pigment extracted from the curable composition is dispersed in purified water containing a surfactant to obtain a dispersion. In the volume-based particle size distribution measured with a laser diffraction particle size distribution measuring apparatus (for example, Shimadzu Corporation, SALD-3000J) using this dispersion, the value when the integration from the small diameter side is 50% ( The median diameter (D50)) is defined as the average particle diameter of the white pigment. As a method for extracting the white pigment from the curable composition, for example, the curable composition can be obtained by diluting the curable composition with a liquid medium, precipitating the white pigment by a centrifugal treatment or the like, and collecting the white pigment.
In addition, the average particle diameter of the white pigment contained in the cured product is calculated by calculating the equivalent circle diameter (the geometric average of the major axis and the minor axis) for 50 particles by observing the particles using a scanning electron microscope. It can be obtained as an arithmetic average value.
　硬化性組成物が白色顔料を含む場合、硬化性組成物中で白色顔料が凝集することを抑制する観点から、白色粒子は、表面の少なくとも一部に有機物を含む有機物層を有することが好ましい。有機物層に含まれる有機物としては、有機シラン、オルガノシロキサン、フルオロシラン、有機ホスホネート、有機リン酸化合物、有機ホスフィネート、有機スルホン酸化合物、カルボン酸、カルボン酸エステル、カルボン酸の誘導体、アミド、炭化水素ワックス、ポリオレフィン、ポリオレフィンのコポリマー、ポリオール、ポリオールの誘導体、アルカノールアミン、アルカノールアミンの誘導体、有機分散剤等が挙げられる。
　有機物層に含まれる有機物は、ポリオール、有機シラン等を含むことが好ましく、ポリオール又は有機シランの少なくとも一方を含むことがより好ましい。
　有機シランの具体例としては、オクチルトリエトキシシラン、ノニルトリエトキシシラン、デシルトリエトキシシラン、ドデシルトリエトキシシラン、トリデシルトリエトキシシラン、テトラデシルトリエトキシシラン、ペンタデシルトリエトキシシラン、ヘキサデシルトリエトキシシラン、ヘプタデシルトリエトキシシラン、オクタデシルトリエトキシシラン等が挙げられる。
　オルガノシロキサンの具体例としては、トリメチルシリル官能基で終端されたポリジメチルシロキサン（ＰＤＭＳ）、ポリメチルヒドロシロキサン（ＰＭＨＳ）、ＰＭＨＳのオレフィンによる官能化（ヒドロシリル化による）により誘導されるポリシロキサン等が挙げられる。
　有機ホスホネートの具体例としては、例えば、ｎ－オクチルホスホン酸及びそのエステル、ｎ－デシルホスホン酸及びそのエステル、２－エチルヘキシルホスホン酸及びそのエステル並びにカンフィル（ｃａｍｐｈｙｌ）ホスホン酸及びそのエステルが挙げられる。
　有機リン酸化合物の具体例としては、有機酸性ホスフェート、有機ピロホスフェート、有機ポリホスフェート、有機メタホスフェート、これらの塩等が挙げられる。
　有機ホスフィネートの具体例としては、例えば、ｎ－ヘキシルホスフィン酸及びそのエステル、ｎ－オクチルホスフィン酸及びそのエステル、ジ－ｎ－ヘキシルホスフィン酸及びそのエステル並びにジ－ｎ－オクチルホスフィン酸及びそのエステルが挙げられる。
　有機スルホン酸化合物の具体例としては、ヘキシルスルホン酸、オクチルスルホン酸、２－エチルヘキシルスルホン酸等のアルキルスルホン酸、これらアルキルスルホン酸と、ナトリウム、カルシウム、マグネシウム、アルミニウム、チタン等の金属イオン、アンモニウムイオン、トリエタノールアミン等の有機アンモニウムイオンなどとの塩が挙げられる。
　カルボン酸の具体例としては、マレイン酸、マロン酸、フマル酸、安息香酸、フタル酸、ステアリン酸、オレイン酸、リノール酸等が挙げられる。
　カルボン酸エステルの具体例としては、上記カルボン酸と、エチレングリコール、プロピレングリコール、トリメチロールプロパン、ジエタノールアミン、トリエタノールアミン、グリセロール、ヘキサントリオール、エリトリトール、マンニトール、ソルビトール、ペンタエリトリトール、ビスフェノールＡ、ヒドロキノン、フロログルシノール等のヒドロキシ化合物との反応により生成するエステル及び部分エステルが挙げられる。
　アミドの具体例としては、ステアリン酸アミド、オレイン酸アミド、エルカ酸アミド等が挙げられる。
　ポリオレフィン及びそのコポリマーの具体例としては、ポリエチレン、ポリプロピレン、エチレンと、プロピレン、ブチレン、酢酸ビニル、アクリレート、アクリルアミド等から選択される１種又は２種以上の化合物との共重合体などが挙げられる。
　ポリオールの具体例としては、グリセロール、トリメチロールエタン、トリメチロールプロパン等が挙げられる。
　アルカノールアミンの具体例としては、ジエタノールアミン、トリエタノールアミン等が挙げられる。
　有機分散剤の具体例としては、クエン酸、ポリアクリル酸、ポリメタクリル酸、陰イオン性、陽イオン性、双性、非イオン性等の官能基をもつ高分子有機分散剤などが挙げられる。
　硬化性組成物中における白色顔料の凝集が抑制されると、硬化物中における白色顔料の分散性が向上する傾向にある。 When the curable composition contains a white pigment, the white particles preferably have an organic layer containing an organic substance on at least a part of the surface from the viewpoint of suppressing aggregation of the white pigment in the curable composition. Organic substances contained in the organic layer include organic silane, organosiloxane, fluorosilane, organic phosphonate, organic phosphoric acid compound, organic phosphinate, organic sulfonic acid compound, carboxylic acid, carboxylic acid ester, carboxylic acid derivative, amide, hydrocarbon Examples thereof include waxes, polyolefins, polyolefin copolymers, polyols, polyol derivatives, alkanolamines, alkanolamine derivatives, and organic dispersants.
The organic material contained in the organic material layer preferably contains a polyol, an organic silane, or the like, and more preferably contains at least one of a polyol or an organic silane.
Specific examples of the organic silane include octyltriethoxysilane, nonyltriethoxysilane, decyltriethoxysilane, dodecyltriethoxysilane, tridecyltriethoxysilane, tetradecyltriethoxysilane, pentadecyltriethoxysilane, hexadecyltriethoxy Silane, heptadecyltriethoxysilane, octadecyltriethoxysilane, etc. are mentioned.
Specific examples of organosiloxanes include polydimethylsiloxane terminated with a trimethylsilyl functional group (PDMS), polymethylhydrosiloxane (PMHS), polysiloxane derived by functionalization of PMHS with an olefin (by hydrosilylation), and the like. It is done.
Specific examples of the organic phosphonate include, for example, n-octyl phosphonic acid and its ester, n-decyl phosphonic acid and its ester, 2-ethylhexyl phosphonic acid and its ester, and camphyl phosphonic acid and its ester.
Specific examples of the organic phosphate compound include organic acidic phosphates, organic pyrophosphates, organic polyphosphates, organic metaphosphates, salts thereof, and the like.
Specific examples of the organic phosphinate include n-hexylphosphinic acid and its ester, n-octylphosphinic acid and its ester, di-n-hexylphosphinic acid and its ester, and di-n-octylphosphinic acid and its ester. Can be mentioned.
Specific examples of the organic sulfonic acid compound include hexyl sulfonic acid, octyl sulfonic acid, alkyl sulfonic acid such as 2-ethylhexyl sulfonic acid, these alkyl sulfonic acids and metal ions such as sodium, calcium, magnesium, aluminum and titanium, ammonium And salts with organic ammonium ions such as ions and triethanolamine.
Specific examples of the carboxylic acid include maleic acid, malonic acid, fumaric acid, benzoic acid, phthalic acid, stearic acid, oleic acid, linoleic acid and the like.
Specific examples of the carboxylic acid ester include the above carboxylic acid and ethylene glycol, propylene glycol, trimethylolpropane, diethanolamine, triethanolamine, glycerol, hexanetriol, erythritol, mannitol, sorbitol, pentaerythritol, bisphenol A, hydroquinone, furoquinone, Examples thereof include esters and partial esters formed by reaction with hydroxy compounds such as loglucinol.
Specific examples of the amide include stearic acid amide, oleic acid amide, erucic acid amide and the like.
Specific examples of the polyolefin and its copolymer include a copolymer of polyethylene, polypropylene, ethylene and one or more compounds selected from propylene, butylene, vinyl acetate, acrylate, acrylamide, and the like.
Specific examples of the polyol include glycerol, trimethylol ethane, trimethylol propane and the like.
Specific examples of the alkanolamine include diethanolamine and triethanolamine.
Specific examples of organic dispersants include citric acid, polyacrylic acid, polymethacrylic acid, high molecular organic dispersants having functional groups such as anionic, cationic, zwitterionic, and nonionic.
When aggregation of the white pigment in the curable composition is suppressed, the dispersibility of the white pigment in the cured product tends to be improved.
　白色顔料は、表面の少なくとも一部に金属酸化物を含む金属酸化物層を有していてもよい。金属酸化物層に含まれる金属酸化物としては、二酸化ケイ素、酸化アルミニウム、ジルコニア、ホスホリア（ｐｈｏｓｐｈｏｒｉａ）、ボリア（ｂｏｒｉａ）等が挙げられる。金属酸化物層は一層であっても二層以上であってもよい。白色顔料が二層の金属酸化物層を有する場合、二酸化ケイ素を含む第一金属酸化物層及び酸化アルミニウムを含む第二金属酸化物層を含むものであることが好ましい。
　白色顔料が金属酸化物層を有することで、脂環式構造とスルフィド構造とを含む硬化物中における白色顔料の分散性が向上する傾向にある。 The white pigment may have a metal oxide layer containing a metal oxide on at least a part of the surface. Examples of the metal oxide contained in the metal oxide layer include silicon dioxide, aluminum oxide, zirconia, phosphoria, and boria. The metal oxide layer may be a single layer or two or more layers. When the white pigment has two metal oxide layers, the white pigment preferably includes a first metal oxide layer containing silicon dioxide and a second metal oxide layer containing aluminum oxide.
When the white pigment has a metal oxide layer, the dispersibility of the white pigment in a cured product containing an alicyclic structure and a sulfide structure tends to be improved.
　白色顔料は、有機物層と金属酸化物層とを有するものであってもよい。この場合、白色顔料の表面に、金属酸化物層及び有機物層が、金属酸化物層及び有機物層の順に設けられることが好ましい。白色顔料が有機物層と二層の金属酸化物層とを有するものである場合、白色顔料の表面に、二酸化ケイ素を含む第一金属酸化物層、酸化アルミニウムを含む第二金属酸化物層及び有機物層が、第一金属酸化物層、第二金属酸化物層及び有機物層の順に設けられることが好ましい。 The white pigment may have an organic layer and a metal oxide layer. In this case, it is preferable that the metal oxide layer and the organic material layer are provided in the order of the metal oxide layer and the organic material layer on the surface of the white pigment. When the white pigment has an organic material layer and two metal oxide layers, the surface of the white pigment has a first metal oxide layer containing silicon dioxide, a second metal oxide layer containing aluminum oxide, and an organic material. It is preferable that a layer is provided in order of a 1st metal oxide layer, a 2nd metal oxide layer, and an organic substance layer.
　硬化性組成物が白色顔料を含む場合、硬化性組成物中の白色顔料の含有率は、硬化性組成物の全量に対して、例えば、０．０５質量％～１．０質量％であることが好ましく、０．１質量％～１．０質量％であることがより好ましく、０．２質量％～０．５質量％であることがさらに好ましい。 When the curable composition contains a white pigment, the content of the white pigment in the curable composition is, for example, 0.05% by mass to 1.0% by mass with respect to the total amount of the curable composition. It is preferably 0.1% by mass to 1.0% by mass, and more preferably 0.2% by mass to 0.5% by mass.
（その他の成分）
　硬化性組成物は、重合禁止剤、シランカップリング剤、界面活性剤、密着付与剤、酸化防止剤等のその他の成分をさらに含んでいてもよい。硬化性組成物は、その他の成分のそれぞれについて、１種類を単独で含んでいてもよく、２種類以上を組み合わせて含んでいてもよい。
　また、硬化性組成物は、必要に応じて（メタ）アリル化合物を含んでいてもよい。 (Other ingredients)
The curable composition may further contain other components such as a polymerization inhibitor, a silane coupling agent, a surfactant, an adhesion imparting agent, and an antioxidant. The curable composition may contain one kind of each of other components, or may contain two or more kinds in combination.
Moreover, the curable composition may contain the (meth) allyl compound as needed.
（硬化性組成物の調製方法）
　硬化性組成物は、例えば、量子ドット蛍光体、アルキレンオキシ基及び重合性反応基を有するアルキレンオキシ基含有化合物、多官能チオール化合物並びに光重合開始剤並びに必要に応じて前述した成分を常法により混合することで調製することができる。量子ドット蛍光体は、分散媒体に分散させた状態で混合することが好ましい。 (Method for preparing curable composition)
The curable composition may be prepared by, for example, a quantum dot phosphor, an alkyleneoxy group-containing compound having an alkyleneoxy group and a polymerizable reactive group, a polyfunctional thiol compound, a photopolymerization initiator, and, if necessary, the above-described components according to a conventional method. It can be prepared by mixing. The quantum dot phosphor is preferably mixed while being dispersed in a dispersion medium.
（硬化性組成物の用途）
　硬化性組成物は、フィルム形成に好適に使用可能である。また、硬化性組成物は、波長変換部材の形成に好適に使用可能である。 (Use of curable composition)
The curable composition can be suitably used for film formation. Moreover, a curable composition can be used conveniently for formation of a wavelength conversion member.
　以下、本発明を実施例により具体的に説明するが、本発明はこれらの実施例に限定されるものではない。 Hereinafter, the present invention will be specifically described by way of examples. However, the present invention is not limited to these examples.
＜実施例１～４並びに比較例１及び２＞
（硬化性組成物の調製）
　表１に示す各成分を同表に示す配合量（単位：質量部）で混合することにより、実施例１～５並びに比較例１及び２の硬化性組成物をそれぞれ調製した。表１中の「－」は未配合を意味する。
　なお、脂環式構造を有する多官能（メタ）アクリレート化合物（比較用化合物）として、トリシクロデカンジメタノールジアクリレート（新中村化学工業株式会社、Ａ－ＤＣＰ）を用い、アルキレンオキシ基含有化合物としては、エトキシ化ビスフェノールＡジアクリレート（新中村化学工業株式会社、ＡＢＥ－３００）を用いた。
　また、多官能チオール化合物として、ペンタエリスリトールテトラキス（３－メルカプトプロピオネート）（ＳＣ有機化学株式会社、ＰＥＭＰ）を用いた。
　また、光重合開始剤としては、２，４，６－トリメチルベンゾイル－ジフェニル－フォスフィンオキサイド（ＢＡＳＦ社、ＩＲＧＡＣＵＲＥ　ＴＰＯ）を用いた。
　また、量子ドット蛍光体ＩＢＯＡ（イソボルニルアクリレート）分散液として、ＣｄＳｅ／ＺｎＳ（コア／シェル）分散液（Ｎａｎｏｓｙｓ社、Ｇｅｎ３．５　ＱＤ　Ｃｏｎｃｅｎｔｒａｔｅ）を用いた。このＣｄＳｅ／ＺｎＳ（コア／シェル）分散液の分散媒体としては、イソボルニルアクリレートを使用した。ＣｄＳｅ／ＺｎＳ（コア／シェル）分散液中に、イソボルニルアクリレートが９０質量％以上含有されている。
　また、カルボン酸として、酢酸を用いた。
　また、白色顔料として、酸化チタン（Ｃｈｅｍｏｕｒｓ社、タイピュア　Ｒ－７０６、粒子径０．３６μｍ）を用いた。酸化チタンの表面には、酸化ケイ素を含む第一金属酸化物層、酸化アルミニウムを含む第二金属酸化物層及びポリオール化合物を含む有機物層が、第一金属酸化物層、第二金属酸化物層及び有機物層の順に設けられている。 <Examples 1 to 4 and Comparative Examples 1 and 2>
(Preparation of curable composition)
The curable compositions of Examples 1 to 5 and Comparative Examples 1 and 2 were prepared by mixing the components shown in Table 1 in the blending amounts (unit: parts by mass) shown in the same table. "-" In Table 1 means not blended.
Tricyclodecane dimethanol diacrylate (Shin Nakamura Chemical Co., Ltd., A-DCP) was used as the polyfunctional (meth) acrylate compound (comparative compound) having an alicyclic structure, and as an alkyleneoxy group-containing compound. Used ethoxylated bisphenol A diacrylate (Shin Nakamura Chemical Co., Ltd., ABE-300).
In addition, pentaerythritol tetrakis (3-mercaptopropionate) (SC Organic Chemical Co., PEMP) was used as the polyfunctional thiol compound.
As a photopolymerization initiator, 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide (BASF, IRGACURE TPO) was used.
Further, a CdSe / ZnS (core / shell) dispersion (Nanosys, Gen 3.5 QD Concentrate) was used as the quantum dot phosphor IBOA (isobornyl acrylate) dispersion. Isobornyl acrylate was used as a dispersion medium for this CdSe / ZnS (core / shell) dispersion. 90% by mass or more of isobornyl acrylate is contained in the CdSe / ZnS (core / shell) dispersion.
Acetic acid was used as the carboxylic acid.
In addition, titanium oxide (Chemours, Taipure R-706, particle size 0.36 μm) was used as a white pigment. On the surface of titanium oxide, a first metal oxide layer containing silicon oxide, a second metal oxide layer containing aluminum oxide, and an organic material layer containing a polyol compound are formed into a first metal oxide layer and a second metal oxide layer. And an organic material layer.
Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001
（波長変換部材の製造）
　上記で得られた各硬化性組成物を平均厚み１００μｍのＰＥＴフィルム（東洋紡株式会社）（被覆材）上に塗布して塗膜を形成した。この塗膜上に厚み１００μｍのＰＥＴフィルム（東洋紡株式会社）（被覆材）を貼り合わせ、紫外線照射装置（アイグラフィックス株式会社）を用いて紫外線を照射（照射量：１０００ｍＪ／ｃｍ２）することにより、硬化物の両面に被覆材が配置された波長変換部材をそれぞれ得た。 (Manufacture of wavelength conversion member)
Each curable composition obtained above was applied onto a PET film (Toyobo Co., Ltd.) (covering material) having an average thickness of 100 μm to form a coating film. A 100 μm-thick PET film (Toyobo Co., Ltd.) (coating material) is bonded onto this coating film and irradiated with ultraviolet rays (irradiation amount: 1000 mJ / cm 2 ) using an ultraviolet irradiation device (I Graphics Co., Ltd.). Thereby, the wavelength conversion member by which the coating material was arrange | positioned on both surfaces of hardened | cured material was obtained, respectively.
＜評価＞
　実施例１～４並びに比較例１及び２で得られた波長変換部材を用いて、以下の各評価項目を測定及び評価した。結果を表２に示す。 <Evaluation>
Using the wavelength conversion members obtained in Examples 1 to 4 and Comparative Examples 1 and 2, the following evaluation items were measured and evaluated. The results are shown in Table 2.
（耐湿熱性）
　上記で得られた各波長変換部材を、直径１７ｍｍの寸法に裁断し、評価用サンプルを準備した。評価用サンプルについてファイバマルチチャンネル分光器（オーシャンフォトニクス株式会社、オーシャンビュー）にて初期の発光強度の測定を行った。次に、評価用サンプルを８５℃、９５％ＲＨ（相対湿度）環境下の恒温恒湿槽に投入して１０００時間静置した後、発光強度の測定を行った。下記式に従って波長変換部材の相対発光強度保持率を算出した。
　　相対発光強度保持率：（ＲＬｂ／ＲＬａ）×１００
　　　ＲＬａ：初期相対発光強度
　　　ＲＬｂ：８５℃、９５％ＲＨ環境下での１０００時間後の相対発光強度
　なお、相対発光強度保持率の数値が高いほど波長変換部材は耐湿熱性に優れている。 (Moisture and heat resistance)
Each wavelength conversion member obtained above was cut into a 17 mm diameter to prepare a sample for evaluation. The initial emission intensity of the sample for evaluation was measured with a fiber multichannel spectrometer (Ocean Photonics Co., Ltd., Ocean View). Next, the sample for evaluation was put into a constant temperature and humidity chamber under an environment of 85 ° C. and 95% RH (relative humidity) and allowed to stand for 1000 hours, and then the emission intensity was measured. The relative light emission intensity retention rate of the wavelength conversion member was calculated according to the following formula.
Relative emission intensity retention rate: (RLb / RLa) × 100
RLa: Initial relative light emission intensity RLb: Relative light emission intensity after 1000 hours in an environment of 85 ° C. and 95% RH Note that the higher the value of the relative light emission intensity retention rate, the better the wavelength conversion member is in heat and moisture resistance.
（極性成分の測定）
　上記で得られた各波長変換部材の両面のＰＥＴフィルムを剥離し、接触角計（共和界面科学株式会社、ＤＭ－７０１）を用いてジヨードメタンと水の２液に対する硬化物の接触角を測定した。液適量はそれぞれ０．５μＬとして接触角は２θ法により算出した。測定したジヨードメタン接触角及び水の接触角に基づき、解析ソフトウェア（共和界面科学株式会社、ＦＡＭＡＳ)を用いてＷｕの式より極性成分（ｍＪ／ｍ２）を算出した。 (Measurement of polar components)
The PET films on both sides of each wavelength conversion member obtained above were peeled off, and the contact angle of the cured product with respect to two liquids of diiodomethane and water was measured using a contact angle meter (Kyowa Interface Science Co., Ltd., DM-701). . The appropriate amount of liquid was 0.5 μL, and the contact angle was calculated by the 2θ method. Based on the measured diiodomethane contact angle and water contact angle, the polar component (mJ / m 2 ) was calculated from the Wu equation using analysis software (Kyowa Interface Science Co., Ltd., FAMAS).
（透湿度）
　上記で得られた各波長変換部材のＰＥＴフィルムを剥離して得られた硬化物について、ＪＩＳ　Ｚ　０２０８：１９７６の測定法に準拠して透湿度の測定を行った。具体的には、透湿カップに塩化カルシウム１０ｇを測りとり、暴露している部分が直径６ｃｍとなるように透湿カップに各硬化物を固定し、４０℃、相対湿度７０％の条件下で２４時間静置させた際の硬化物の質量変化より透湿度を算出した。 (Moisture permeability)
About the hardened | cured material obtained by peeling the PET film of each wavelength conversion member obtained above, the moisture permeability was measured based on the measuring method of JIS Z 0208: 1976. Specifically, 10 g of calcium chloride is measured in a moisture permeable cup, each cured product is fixed to the moisture permeable cup so that the exposed portion has a diameter of 6 cm, and the conditions are 40 ° C. and 70% relative humidity. The moisture permeability was calculated from the mass change of the cured product when allowed to stand for 24 hours.
（ガラス転移温度）
　上記で得られた各波長変換部材のＰＥＴフィルムを剥離し、幅５ｍｍ、長さ４０ｍｍの寸法に裁断して評価用硬化物を得た。そして、広域動的粘弾性測定装置（Ｒｈｅｏｍｅｔｒｉｃ　Ｓｃｉｅｎｔｉｆｉｃ社、Ｓｏｌｉｄ　Ａｎａｌｙｚｅｒ　ＲＳＡ－ＩＩＩ）を用いて、「引張モード、チャック間距離：２５ｍｍ、周波数：１０Ｈｚ、測定温度範囲：－２０℃～１８０℃、昇温速度：１０℃／分」の条件で、評価用硬化物の貯蔵弾性率（Ｅ’）及び損失弾性率（Ｅ’’）を測定し、その比から損失正接（ｔａｎδ）を求め、損失正接（ｔａｎδ）のピークトップ部分の温度からガラス転移温度（Ｔｇ）を求めた。 (Glass-transition temperature)
The PET film of each wavelength conversion member obtained above was peeled off and cut into dimensions of 5 mm in width and 40 mm in length to obtain a cured product for evaluation. Then, using a wide-range dynamic viscoelasticity measuring apparatus (Rheometric Scientific, Solid Analyzer RSA-III), “tensile mode, distance between chucks: 25 mm, frequency: 10 Hz, measurement temperature range: −20 ° C. to 180 ° C., ascending The storage elastic modulus (E ′) and loss elastic modulus (E ″) of the cured product for evaluation were measured under the condition of “temperature rate: 10 ° C./min”, and the loss tangent (tan δ) was obtained from the ratio, and the loss tangent The glass transition temperature (Tg) was determined from the temperature at the peak top portion of (tan δ).
（ＦＴ－ＩＲピーク面積比率（Ｖ１／Ｖ２））
　上記で得られた各波長変換部材のＰＥＴフィルムを剥離しＦＴ－ＩＲ　Ｓｐｅｃｔｒｏｍｅｔｅｒ（Ｐｅｒｋｉｎ　Ｅｌｍｅｒ社）を用いて、硬化物の表面をＡＴＲ分析した。バックグラウンド測定は、空気で測定し、積算回数１６回の条件でＦＴ－ＩＲ測定を実施し、下記式に従ってＦＴ－ＩＲピーク面積比率を算出した。なお、比較例２では、多官能チオール化合物を使用していないため、ＡＴＲ分析を行っていない。
ＦＴ－ＩＲピーク面積比率：Ｖ１／Ｖ２
Ｖ１：Ｃ＝Ｃ伸縮振動に帰属されるピーク（ピーク波長：１６３７ｃｍ－１）のピーク面積
Ｖ２：Ｓ－Ｈ伸縮振動に帰属されるピーク（ピーク波長：２５７０ｃｍ－１）のピーク面積 (FT-IR peak area ratio (V1 / V2))
The PET film of each wavelength conversion member obtained above was peeled off, and the surface of the cured product was subjected to ATR analysis using FT-IR Spectrometer (Perkin Elmer). For background measurement, measurement was performed with air, FT-IR measurement was performed under the condition of 16 integrations, and the FT-IR peak area ratio was calculated according to the following formula. In Comparative Example 2, since no polyfunctional thiol compound is used, ATR analysis is not performed.
FT-IR peak area ratio: V1 / V2
V1: Peak area of a peak attributed to C = C stretching vibration (peak wavelength: 1637 cm −1 ) V2: Peak area of a peak attributed to SH stretching vibration (peak wavelength: 2570 cm −1 )
Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000002
　表２から分かるように、実施例１～４にて硬化物がアルキレンオキシ構造を有することにより、耐湿熱性の指標である相対発光強度保持率が改善することがわかった。これは、極性の高い硬化物中の樹脂に非極性の酸素が溶解しにくくなったため、高温高湿環境下にて量子ドット蛍光体の酸化劣化が抑制されたことに起因すると推測される。
　一方、実施例２～４では、極性成分が増加すると、相対発光強度保持率が低下する傾向が見られた。この理由は、硬化物のＴｇが低下することにより、硬化物の凝集力が低下したため、硬化物における酸素の透過性が上昇してしまったことが原因であると推測される。 As can be seen from Table 2, it was found that, in Examples 1 to 4, the cured product had an alkyleneoxy structure, thereby improving the relative light emission intensity retention rate, which is an index of moisture and heat resistance. This is presumed to be due to the fact that non-polar oxygen is less likely to dissolve in the resin in the highly polar cured product, so that the oxidative deterioration of the quantum dot phosphor is suppressed in a high temperature and high humidity environment.
On the other hand, in Examples 2 to 4, when the polar component increased, the relative light emission intensity retention rate tended to decrease. The reason for this is presumed to be that oxygen permeability in the cured product has increased since the cohesive force of the cured product has decreased due to a decrease in the Tg of the cured product.
　本明細書に記載された全ての文献、特許出願、及び技術規格は、個々の文献、特許出願、及び技術規格が参照により取り込まれることが具体的かつ個々に記された場合と同程度に、本明細書中に参照により取り込まれる。 All documents, patent applications, and technical standards mentioned in this specification are to the same extent as if each individual document, patent application, and technical standard were specifically and individually stated to be incorporated by reference, Incorporated herein by reference.

Claims (17)

  1. 　量子ドット蛍光体を含み、アルキレンオキシ構造を有する硬化物を備える、波長変換部材。 A wavelength conversion member comprising a cured product including a quantum dot phosphor and having an alkyleneoxy structure.
  2. 　前記硬化物は、スルフィド構造を有する、請求項１に記載の波長変換部材。 The wavelength conversion member according to claim 1, wherein the cured product has a sulfide structure.
  3. 　前記量子ドット蛍光体がＣｄ及びＩｎの少なくとも一方を含む化合物を含む、請求項１又は請求項２に記載の波長変換部材。 The wavelength conversion member according to claim 1 or 2, wherein the quantum dot phosphor includes a compound containing at least one of Cd and In.
  4. 　前記硬化物の少なくとも一部を被覆する被覆材をさらに有する、請求項１～請求項３のいずれか１項に記載の波長変換部材。 The wavelength conversion member according to any one of claims 1 to 3, further comprising a covering material that covers at least a part of the cured product.
  5. 　前記硬化物におけるジヨードメタンの接触角及び水の接触角を用い、Ｗｕの式より算出される極性成分は、５ｍＪ／ｍ２～１２ｍＪ／ｍ２である、請求項１～請求項４のいずれか１項に記載の波長変換部材。 The polar component calculated from the formula of Wu using the contact angle of diiodomethane and the contact angle of water in the cured product is 5 mJ / m 2 to 12 mJ / m 2. The wavelength conversion member according to item.
  6. 　フーリエ変換赤外分光光度計で測定した前記硬化物における、Ｃ＝Ｃ伸縮振動に帰属されるピーク面積（Ｖ１）と、Ｓ－Ｈ伸縮振動に帰属されるピーク面積（Ｖ２）との比率（Ｖ１／Ｖ２）が、０．０００５２以下である、請求項１～請求項５のいずれか１項に記載の波長変換部材。 The ratio (V1) of the peak area (V1) attributed to C = C stretching vibration and the peak area (V2) attributed to SH stretching vibration in the cured product measured with a Fourier transform infrared spectrophotometer The wavelength conversion member according to any one of claims 1 to 5, wherein / V2) is 0.00052 or less.
  7. 　動的粘弾性測定により測定された前記硬化物のガラス転移温度が、４７℃以下である請求項１～請求項６のいずれか１項に記載の波長変換部材。 The wavelength conversion member according to any one of claims 1 to 6, wherein a glass transition temperature of the cured product measured by dynamic viscoelasticity measurement is 47 ° C or lower.
  8. 　請求項１～請求項７のいずれか１項に記載の波長変換部材と、光源とを備えるバックライトユニット。 A backlight unit comprising the wavelength conversion member according to any one of claims 1 to 7 and a light source.
  9. 　請求項８に記載のバックライトユニットを備える画像表示装置。 An image display device comprising the backlight unit according to claim 8.
  10. 　量子ドット蛍光体、アルキレンオキシ基及び重合性反応基を有するアルキレンオキシ基含有化合物並びに光重合開始剤を含む、硬化性組成物。 A curable composition comprising a quantum dot phosphor, an alkyleneoxy group-containing compound having an alkyleneoxy group and a polymerizable reactive group, and a photopolymerization initiator.
  11. 　多官能チオール化合物をさらに含む、請求項１０に記載の硬化性組成物。 The curable composition according to claim 10, further comprising a polyfunctional thiol compound.
  12. 　前記多官能チオール化合物の含有率は、前記硬化性組成物の全量に対して１５質量％～７０質量％である、請求項１１に記載の硬化性組成物。 The curable composition according to claim 11, wherein the content of the polyfunctional thiol compound is 15% by mass to 70% by mass with respect to the total amount of the curable composition.
  13. 　前記アルキレンオキシ基含有化合物中の重合性反応基の数に対する前記多官能チオール化合物中のチオール基の数の比率（チオール基の数／重合性反応基の数）は、０．５～５．０である、請求項１１又は請求項１２に記載の硬化性組成物。 The ratio of the number of thiol groups in the polyfunctional thiol compound to the number of polymerizable reactive groups in the alkyleneoxy group-containing compound (the number of thiol groups / the number of polymerizable reactive groups) is 0.5 to 5.0. The curable composition according to claim 11 or 12, which is
  14. 　前記アルキレンオキシ基含有化合物の含有率は、前記硬化性組成物の全量に対して３０質量％～７０質量％である、請求項１０～請求項１３のいずれか１項に記載の硬化性組成物。 The curable composition according to any one of claims 10 to 13, wherein the content of the alkyleneoxy group-containing compound is 30% by mass to 70% by mass with respect to the total amount of the curable composition. .
  15. 　前記重合性反応基は、（メタ）アクリロイル基を含む、請求項１０～請求項１４のいずれか１項に記載の硬化性組成物。 The curable composition according to any one of claims 10 to 14, wherein the polymerizable reactive group includes a (meth) acryloyl group.
  16. 　炭素数１～１７であるカルボン酸をさらに含む、請求項１０～請求項１５のいずれか１項に記載の硬化性組成物。 The curable composition according to any one of claims 10 to 15, further comprising a carboxylic acid having 1 to 17 carbon atoms.
  17. 　白色顔料をさらに含む、請求項１０～請求項１６のいずれか１項に記載の硬化性組成物。 The curable composition according to any one of claims 10 to 16, further comprising a white pigment.
PCT/JP2018/012588 2018-03-27 2018-03-27 Wavelength conversion member, backlight unit, image display device and curable composition WO2019186733A1 (en)

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