WO2016088815A1 - テトラメチルビフェノール型エポキシ樹脂、エポキシ樹脂組成物、硬化物及び半導体封止材 - Google Patents
テトラメチルビフェノール型エポキシ樹脂、エポキシ樹脂組成物、硬化物及び半導体封止材 Download PDFInfo
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- WO2016088815A1 WO2016088815A1 PCT/JP2015/083939 JP2015083939W WO2016088815A1 WO 2016088815 A1 WO2016088815 A1 WO 2016088815A1 JP 2015083939 W JP2015083939 W JP 2015083939W WO 2016088815 A1 WO2016088815 A1 WO 2016088815A1
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- epoxy resin
- resin composition
- type epoxy
- tetramethylbiphenol
- curing
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Oc1ccccc1 Chemical compound Oc1ccccc1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 7
- NUYLFYAGVDFBLW-UHFFFAOYSA-N CCC(C)(CC)Cc1ccc(CC)cc1 Chemical compound CCC(C)(CC)Cc1ccc(CC)cc1 NUYLFYAGVDFBLW-UHFFFAOYSA-N 0.000 description 1
- XWAZGKYQEXGEGI-UHFFFAOYSA-N CCC1C=CC(CC(C)(C)CC)=CC1 Chemical compound CCC1C=CC(CC(C)(C)CC)=CC1 XWAZGKYQEXGEGI-UHFFFAOYSA-N 0.000 description 1
- FMHWAAZOTFVMKR-UHFFFAOYSA-N CCc1ccc(CC(C)C)cc1 Chemical compound CCc1ccc(CC(C)C)cc1 FMHWAAZOTFVMKR-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N c1ccccc1 Chemical compound c1ccccc1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
- H01L23/29—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
- H01L23/293—Organic, e.g. plastic
- H01L23/295—Organic, e.g. plastic containing a filler
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/24—Di-epoxy compounds carbocyclic
- C08G59/245—Di-epoxy compounds carbocyclic aromatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/62—Alcohols or phenols
- C08G59/621—Phenols
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/68—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
- C08G59/688—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used containing phosphorus
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
- H01L23/29—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
- H01L23/293—Organic, e.g. plastic
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
- H01L23/31—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the arrangement or shape
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
Definitions
- the present invention relates to a tetramethylbiphenol type epoxy resin containing a predetermined amount of sodium ions.
- the present invention also relates to an epoxy resin composition containing a predetermined amount of sodium ions and a cured product obtained by curing the epoxy resin composition. Furthermore, this invention relates to the semiconductor sealing material containing this epoxy resin composition.
- Epoxy resins are used in a wide range of applications because of their excellent cured properties and ease of handling.
- various types of epoxy resins and their cured properties vary greatly, so that they are properly used according to the purpose of each application.
- epoxy resins are used for semiconductor encapsulation, but with the remarkable development of the electronic industry in recent years, demands for heat resistance and insulation reliability required for electronic devices have become increasingly severe.
- tetramethylbiphenol type epoxy resin is suitable for transfer molding because of its excellent crystallinity, high glass transition temperature (Tg), and low viscosity, and is widely used especially for semiconductor encapsulant applications.
- Tg glass transition temperature
- Viscosity Low Viscosity
- Japanese Unexamined Patent Publication No. 11-29694 Japanese Unexamined Patent Publication No. 2007-246671 Japanese Unexamined Patent Publication No. 2012-224774 Japanese Unexamined Patent Publication No. 58-39677
- an object of the present invention is to provide a tetramethylbiphenol type epoxy resin and an epoxy resin composition excellent in heat resistance.
- the present inventor has obtained a new finding that the tetramethylbiphenol type epoxy resin is not easily affected by sodium ions contained as ionic impurities, and if the amount is small, the influence on reliability is small. This is presumably because the tetramethylbiphenol type epoxy resin has four methyl structures and is excellent in moisture absorption resistance due to the inhibition of water absorption at the ether site.
- a surprising effect that heat resistance is improved by containing sodium ions measured by a specific measurement method in a specific ratio was obtained.
- the gist of the present invention resides in the following [1] to [12].
- Measurement is carried out by atomic absorption spectrometry using a solution obtained by dissolving a sample in N-methylpyrrolidone.
- the tetramethylbiphenol type epoxy resin contains diglycidyl ether of 4,4′-bishydroxy-3,3 ′, 5,5′-tetramethylbiphenyl in any one of [1] to [3] The tetramethylbiphenol type epoxy resin described.
- the phosphorus / curing accelerator content is P / Na molar ratio of 50 or more and less than 900 in terms of phosphorus atom with respect to sodium ions obtained by the following measuring method in the epoxy resin composition.
- a semiconductor encapsulant comprising the epoxy resin composition according to any one of [5] to [11].
- the tetramethylbiphenol type epoxy resin of the present invention has excellent crystallinity, a high glass transition temperature (Tg), low viscosity, and excellent heat resistance and reliability. Moreover, since the epoxy resin composition of this invention has the said effect, it can be applied especially effectively to the field
- the epoxy resin of the present invention is a tetramethylbiphenol type epoxy resin (hereinafter sometimes referred to as “the epoxy resin of the present invention”).
- the tetramethylbiphenol type epoxy resin of the present invention is usually represented by the general formula (I).
- n an integer of 0 to 10.
- n is usually 0 to 10, preferably 0 to 5.
- the epoxy resin of the present invention may be a mixture of a plurality of compounds having different values of n in the general formula (I). Moreover, when it is such a mixture, it does not exclude that the epoxy resin in which the value of n in general formula (I) exceeds 10 contains.
- Tetramethylbiphenol type epoxy resin is superior in crystallinity to other epoxy resins, has a high glass transition temperature (Tg), has low viscosity, low water absorption and low water absorption, Excellent heat resistance and reliability, especially suitable for sealing materials.
- the structure of the epoxy resin of the present invention is not limited, but the biphenol structure is preferably a 4,4′-bishydroxy structure, and the position of the methyl group substituting the phenylene group is ortho-position to the ether bond position. It is preferable that
- tetramethylbiphenol type epoxy resins those containing 4,4'-bishydroxy-3,3 ', 5,5'-tetramethylbiphenyl diglycidyl ether are preferable. Especially, what contains 50 weight% or more of this compound is more preferable, and what contains 80 weight% or more is further more preferable.
- the hydrophobicity as an epoxy resin is improved, and the biphenol structure is a 4,4′-bishydroxy structure. This is because the structure of the epoxy resin becomes rigid, so that it is possible to have the characteristics of high glass transition temperature (Tg) and low viscosity.
- the tetramethylbiphenol type epoxy resin of the present invention contains sodium ions at a ratio of 1 ppm to 12 ppm. By containing 1 to 12 ppm of sodium ions, there is an effect of giving a cured product particularly excellent in heat resistance.
- the tetramethylbiphenol type epoxy resin of the present invention preferably contains sodium ions in a proportion of 1.5 ppm or more, more preferably in a proportion of 2.0 ppm or more, and on the other hand, a proportion of 8.0 ppm or less. It is preferable that it is contained at a ratio of 6.0 ppm or less, more preferably 4.0 ppm or less. If the amount of sodium ion contained in the epoxy resin is too small, the effect of the present invention is difficult to obtain, and if the amount of sodium ion is too large, the electrical reliability tends to be impaired.
- the content of sodium ions contained in the epoxy resin refers to an atomic absorption method [for example, atomic absorption photometer (for example, atomic absorption photometer) after dissolving a sample in N-methylpyrrolidone and atomizing sodium ions contained in the sample. It is the value of the mass standard obtained by measuring by using Hitachi High-Tech Science Co., Ltd. Z-2710). Sodium that is not detected by the measurement method (hereinafter sometimes referred to as “the present measurement method”) is not included in the content of sodium ions in the present invention.
- the means for setting the content of sodium ions contained in the epoxy resin of the present invention to the above range is not limited.
- tetramethylbiphenol type epoxy resin contains sodium ions so as to have a predetermined content. It may be adjusted by adding a compound, and as will be described later, when a compound containing sodium ions is used in the process of producing a tetramethylbiphenol type epoxy resin, the epoxy resin obtained by the reaction is washed. And the degree of post-treatment such as purification may be adjusted.
- the present invention is characterized in that the content is controlled to a specific content within a very narrow range by using the means exemplified above rather than reducing the amount of sodium ions as much as possible.
- the sodium contained in the epoxy resin is (1) whether it is an ion, or (2) whether it is dissolved in a specific solvent. It is also characterized by being defined by the value measured by a specific method.
- Epoxy equivalent of epoxy resin The epoxy resin of the present invention has an epoxy equivalent of not less than 174 g / equivalent and preferably not more than 300 g / equivalent from the viewpoint of handleability as an epoxy resin for a sealing material. From the viewpoint of better handling properties, the epoxy equivalent is 174 g / equivalent or more, and more preferably 200 g / equivalent or less. Among these, 180 g / equivalent or more and 190 g / equivalent or less are more preferable.
- “epoxy equivalent” is defined as “the mass of an epoxy resin containing one equivalent of an epoxy group” and can be measured according to JIS K7236 (2001).
- the epoxy resin of the present invention has a melt viscosity at 150 ° C. of 0.001 Pa ⁇ s or more and preferably 10 Pa ⁇ s or less from the viewpoint of handleability as an epoxy resin for a sealing material, and more handleability. From the viewpoint of improving the melt viscosity, the melt viscosity is 0.001 Pa ⁇ s or more and more preferably 3 Pa ⁇ s or less.
- the “melt viscosity” is a viscosity measured at a rotational speed of 750 rpm by melting an epoxy resin on a hot plate of a cone plate viscometer (manufactured by Tokai Yagami Co., Ltd.) adjusted to 150 ° C. .
- the amount of tetramethylbiphenol used as the raw material for the epoxy resin of the present invention is usually 0.8 to 20 equivalents, preferably 0.9 to 15 equivalents, more preferably 1.0 to 10 equivalents per equivalent of the hydroxyl group.
- an epihalohydrin to make a uniform solution. It is preferable for the amount of epihalohydrin to be equal to or greater than the lower limit because the high molecular weight reaction can be easily controlled and an appropriate melt viscosity can be obtained.
- the amount of epihalohydrin is not more than the above upper limit, production efficiency tends to be improved, which is preferable.
- epichlorohydrin or epibromohydrin is usually used as epihalohydrin in this reaction.
- the amount of alkali metal hydroxide corresponding to 6 equivalents is added as a solid or an aqueous solution and reacted. It is preferable that the amount of the alkali metal hydroxide is equal to or more than the lower limit because the unreacted hydroxyl group and the generated epoxy resin are difficult to react and the high molecular weight reaction is easily controlled. Moreover, it is preferable that the amount of the alkali metal hydroxide is not more than the upper limit value because impurities due to side reactions are not easily generated.
- the alkali metal hydroxide used here sodium hydroxide or potassium hydroxide is usually used, but the epoxy resin containing a predetermined amount of sodium ions is preferably sodium hydroxide as the alkali metal hydroxide.
- the reaction can be carried out under normal pressure or reduced pressure, and the reaction temperature is preferably 40 to 150 ° C., more preferably 40 to 100 ° C., still more preferably 40 to 80 ° C. It is preferable for the reaction temperature to be equal to or higher than the lower limit because the reaction can easily proceed and the reaction can be easily controlled. Further, it is preferable that the reaction temperature is not more than the above upper limit because the side reaction is unlikely to proceed, and in particular, chlorine impurities are easily reduced.
- the reaction liquid is azeotroped while maintaining a predetermined temperature as required, the condensed liquid obtained by cooling the vaporized vapor is separated into oil / water, and the oil component excluding moisture is returned to the reaction system. Is performed while dehydrating.
- the alkali metal hydroxide is preferably intermittently little by little over 0.1 to 8 hours, more preferably 0.1 to 7 hours, and even more preferably 0.5 to 6 hours. Or add continuously.
- the addition time of the alkali metal hydroxide is not less than the lower limit, it is possible to prevent the reaction from proceeding rapidly and to easily control the reaction temperature. It is preferable for the addition time to be less than or equal to the above upper limit because chlorine impurities are less likely to be generated, and it is also preferable from the viewpoint of economy.
- the total reaction time is usually 1 to 15 hours.
- an insoluble by-product salt is filtered off or removed by washing, and then the unreacted epihalohydrin is distilled off under reduced pressure to obtain a tetramethylbiphenol type epoxy resin.
- sodium hydroxide is used as the alkali metal hydroxide, the sodium ion content of the epoxy resin can be adjusted by adjusting the washing conditions.
- a quaternary ammonium salt such as tetramethylammonium chloride or tetraethylammonium bromide; a tertiary amine such as benzyldimethylamine or 2,4,6-tris (dimethylaminomethyl) phenol; 2-ethyl Catalysts such as imidazoles such as -4-methylimidazole or 2-phenylimidazole; phosphonium salts such as ethyltriphenylphosphonium iodide; phosphines such as triphenylphosphine may be used.
- a quaternary ammonium salt such as tetramethylammonium chloride or tetraethylammonium bromide
- a tertiary amine such as benzyldimethylamine or 2,4,6-tris (dimethylaminomethyl) phenol
- 2-ethyl Catalysts such as imid
- alcohols such as ethanol or isopropyl alcohol; ketones such as acetone or methyl ethyl ketone; ethers such as dioxane or ethylene glycol dimethyl ether; glycol ethers such as methoxypropanol; non-dimethyls such as dimethyl sulfoxide or dimethylformamide
- an inert organic solvent such as a protic polar solvent may be used.
- the crude epoxy resin is redissolved in an inert organic solvent such as isopropyl alcohol, methyl ethyl ketone, methyl isobutyl ketone, toluene, xylene, dioxane, methoxypropanol or dimethyl sulfoxide, and the alkali metal hydroxide is solidified.
- an inert organic solvent such as isopropyl alcohol, methyl ethyl ketone, methyl isobutyl ketone, toluene, xylene, dioxane, methoxypropanol or dimethyl sulfoxide
- the alkali metal hydroxide is solidified.
- the dechlorination reaction is performed by adding in an aqueous solution.
- the temperature for the dechlorination reaction is preferably 30 to 120 ° C., more preferably 40 to 110 ° C., still more preferably 50 to 100 ° C., and the reaction time is preferably 0.1 to 15 hours, more preferably 0. 3 to 12 hours, more preferably 0.5 to 10 hours. It is preferable that the reaction temperature of the dechlorination reaction is equal to or higher than the lower limit and the reaction time is equal to or higher than the lower limit because the dechlorination reaction easily proceeds. Moreover, since reaction temperature is below the said upper limit and reaction time is below the said upper limit, since reaction is easy to control, it is preferable.
- the epoxy resin composition of the present invention is an epoxy resin composition containing a tetramethylbiphenol type epoxy resin and a curing agent, and the sodium ion content determined by the following measurement method is 0.6 to 12 ppm. (Measurement method) Measurement is carried out by atomic absorption spectrometry using a solution obtained by dissolving a sample in N-methylpyrrolidone.
- the epoxy resin composition of the present invention is excellent in heat resistance and gives a cured product that sufficiently satisfies various physical properties required for various uses.
- the epoxy resin composition of the present invention contains sodium ions at a ratio of 0.6 ppm to 12 ppm.
- 0.6 to 12 ppm of sodium ions By containing 0.6 to 12 ppm of sodium ions, an effect of giving a cured product having particularly excellent heat resistance is obtained.
- the content of sodium ions contained in the epoxy resin composition in the present invention refers to an atomic absorption method [for example, atomic absorption photometry after dissolving a sample in N-methylpyrrolidone and atomizing sodium ions contained in the sample. It is a mass standard value obtained by measurement using a meter (using Hitachi High-Tech Science Co., Ltd., Z-2710). Sodium that is not detected by the measurement method is not included in the content of sodium ions in the present invention.
- the epoxy resin composition of the present invention may be measured as it is as a sample.
- Each component (for example, tetramethylbiphenol type epoxy resin, curing agent or curing accelerator) contained in the epoxy resin composition of the present invention is measured in advance as a sample, and each component obtained here is measured.
- the content of sodium ions in the composition may be determined from the sodium ion content of the composition and the blending ratio of each component in the composition.
- the means for setting the content of sodium ions contained in the epoxy resin composition of the present invention to the above range is not limited.
- a compound containing sodium ions so as to have a predetermined content in the composition. May be adjusted by adding a tetramethylbiphenol-type epoxy resin, a curing agent or a curing accelerator containing a suitable amount of sodium ions in the composition. .
- the epoxy resin composition of the present invention may further contain an epoxy resin other than the tetramethylbiphenol type epoxy resin (hereinafter sometimes referred to as “other epoxy resin”).
- other epoxy resin an epoxy resin other than the tetramethylbiphenol type epoxy resin
- Examples of the other epoxy resins include bisphenol AD type epoxy resin, hydroquinone type epoxy resin, methyl hydroquinone type epoxy resin, dibutyl hydroquinone type epoxy resin, resorcin type epoxy resin, methyl resorcin type epoxy resin, and tetramethylbisphenol F type epoxy.
- dihydroxydiphenyl ether type epoxy resins epoxy resins derived from thiodiphenols, dihydroxynaphthalene type epoxy resins, dihydroxyanthracene type epoxy resins, dihydroxydihydroanthracene type epoxy resins, dicyclopentadiene type epoxy resins, dihydroxystilbenes Epoxy resin, phenol novolac type epoxy resin, cresol novolac type epoxy resin, screw Enol A novolak type epoxy resin, naphthol novolak type epoxy resin, phenol aralkyl type epoxy resin, naphthol aralkyl type epoxy resin, biphenyl aralkyl type epoxy resin, terpene phenol type epoxy resin, dicyclopentadiene phenol type epoxy resin, phenol hydroxybenzaldehyde Epoxy resins derived from condensates, epoxy resins derived from phenol / crotonaldehyde condensates, epoxy resins derived from phenol / glyo
- the content thereof may be referred to as an epoxy resin (hereinafter referred to as “total epoxy resin component”) as a solid content contained in the epoxy resin composition. .) It is preferably 0.01 to 60 parts by weight with respect to 100 parts by weight, more preferably 40 parts by weight or less, still more preferably 30 parts by weight or less, particularly preferably 20 parts by weight or less, while more preferably 1 It is more than part by weight. That is, it is preferable that at least 40 parts by weight of the tetramethylbiphenol type epoxy resin of the present invention is contained in 100 parts by weight of all epoxy resin components.
- the “total epoxy resin component” corresponds to the amount of the epoxy resin contained in the epoxy resin composition of the present invention, and when the epoxy resin composition of the present invention contains only a tetramethylbiphenol type epoxy resin, The amount of the methyl biphenol type epoxy resin corresponds, and when the tetramethyl biphenol type epoxy resin and other epoxy resins are included, it corresponds to the total of these amounts.
- curing agent shows the substance which contributes to the crosslinking reaction and / or chain length extension reaction between the epoxy groups of an epoxy resin.
- a curing agent even if what is usually called a “curing accelerator” is a substance that contributes to a crosslinking reaction and / or chain extension reaction between epoxy groups of an epoxy resin, it is regarded as a curing agent. To do.
- the curing agent is preferably allowed to act in the range of 0.01 to 1000 parts by weight with respect to 100 parts by weight of all epoxy resin components in the epoxy resin composition of the present invention. More preferable amounts are as described below depending on the type of curing agent.
- curing agent there are no particular limitations on the curing agent, and any of those generally known as epoxy resin curing agents can be used.
- epoxy resin curing agents for example, phenolic curing agents, aliphatic amines, polyether amines, alicyclic amines, aromatic amines, tertiary amines and other amine curing agents, acid anhydride curing agents, amide curing agents, imidazoles, etc. Is mentioned.
- the epoxy resin composition of this invention can give the hardened
- the curing agent preferably contains a phenolic curing agent. From the viewpoint of heat resistance and the like, it is preferable to include an acid anhydride curing agent and an amide curing agent. It is also preferable to use imidazoles from the viewpoint of sufficiently proceeding the curing reaction and improving heat resistance.
- curing agent may be used only by 1 type, or may use 2 or more types by arbitrary combinations and a mixture ratio.
- each component of the curing agent may be used after mixing them in advance to prepare a mixed curing agent, and when mixing each component of the epoxy resin composition, each component of the curing agent may be used. They may be added separately and mixed at the same time.
- phenolic curing agents include bisphenol A, bisphenol F, bisphenol S, bisphenol AD, hydroquinone, resorcin, methylresorcin, biphenol, tetramethylbiphenol, dihydroxynaphthalene, dihydroxydiphenyl ether, thiodiphenols, phenol novolac resin, cresol Novolac resin, phenol aralkyl resin, biphenyl aralkyl resin, naphthol aralkyl resin, terpene phenol resin, dicyclopentadiene phenol resin, bisphenol A novolac resin, trisphenol methane type resin, naphthol novolac resin, brominated bisphenol A and brominated phenol novolac resin
- polyphenols such as various phenols and benzal Polyhydric phenol resins obtained by condensation reaction with various aldehydes such as hydride, hydroxybenzaldehyde, crotonaldehyde and
- a phenol novolak resin for example, a compound represented by the following formula (1)]
- a phenol aralkyl resin for example, the following formula: Compound represented by (2)]
- biphenyl aralkyl resin for example, compound represented by the following formula (3)
- naphthol novolak resin for example, compound represented by the following formula (4)
- naphthol aralkyl resin for example, a compound represented by the following formula (5)], a trisphenol methane type resin [for example, a compound represented by the following formula (6)], a phenol / benzaldehyde / xylylene dimethoxide polycondensate [for example, the following formula Compound represented by (7)], phenol / benzaldehyde / xylylene dihalide polycondensate [for example, represented by the following formula (7) Compound], phenol / benzaldehyde / xylylene dihalide polycondensate [for example,
- k 1 to k 6 each represents a number of 0 or more.
- k 7 , k 8 , l 1 and l 2 each represent a number of 1 or more.
- the blending amount of the phenolic curing agent is preferably 0.1 to 100 parts by weight, more preferably 80 parts by weight or less, and still more preferably 60 parts by weight with respect to 100 parts by weight of all epoxy resin components in the epoxy resin composition. Or less.
- amine curing agent examples include aliphatic amines, polyether amines, alicyclic amines, aromatic amines, and tertiary amines.
- Examples of the aliphatic amines include ethylenediamine, 1,3-diaminopropane, 1,4-diaminopropane, hexamethylenediamine, 2,5-dimethylhexamethylenediamine, trimethylhexamethylenediamine, diethylenetriamine, iminobispropylamine, Examples thereof include bis (hexamethylene) triamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, N-hydroxyethylethylenediamine, and tetra (hydroxyethyl) ethylenediamine.
- polyether amines examples include triethylene glycol diamine, tetraethylene glycol diamine, diethylene glycol bis (propylamine), polyoxypropylene diamine, and polyoxypropylene triamines.
- alicyclic amines examples include isophorone diamine, metacene diamine, N-aminoethylpiperazine, bis (4-amino-3-methyldicyclohexyl) methane, bis (aminomethyl) cyclohexane, 3,9-bis (3 -Aminopropyl) -2,4,8,10-tetraoxaspiro (5,5) undecane and norbornenediamine.
- aromatic amines include tetrachloro-p-xylenediamine, m-xylenediamine, p-xylenediamine, m-phenylenediamine, o-phenylenediamine, p-phenylenediamine, 2,4-diaminoanisole, 2 , 4-toluenediamine, 2,4-diaminodiphenylmethane, 4,4'-diaminodiphenylmethane, 4,4'-diamino-1,2-diphenylethane, 2,4-diaminodiphenylsulfone, 4,4'-diaminodiphenyl Sulfone, m-aminophenol, m-aminobenzylamine, benzyldimethylamine, 2- (dimethylaminomethyl) phenol, triethanolamine, methylbenzylamine, ⁇ - (m-aminophenyl) ethylamine,
- tertiary amine examples include 1,8-diazabicyclo (5,4,0) undecene-7, triethylenediamine, benzyldimethylamine, triethanolamine, dimethylaminoethanol and tris (dimethylaminomethyl) phenol. It is done.
- the amine-based curing agents mentioned above may be used alone or in any combination and blending ratio.
- the amine curing agent is used so that the equivalent ratio of functional groups in the curing agent to epoxy groups in all epoxy resin components contained in the epoxy resin composition is in the range of 0.8 to 1.5. Is preferred. Within this range, unreacted epoxy groups and functional groups of the curing agent are unlikely to remain, which is preferable.
- acid anhydride curing agent examples include acid anhydrides and modified acid anhydrides.
- acid anhydrides include phthalic acid anhydride, trimellitic acid anhydride, pyromellitic acid anhydride, benzophenone tetracarboxylic acid anhydride, dodecenyl succinic acid anhydride, polyadipic acid anhydride, polyazelinic acid anhydride, polysebacic acid Anhydride, poly (ethyloctadecanedioic acid) anhydride, poly (phenylhexadecanedioic acid) anhydride, tetrahydrophthalic anhydride, methyltetrahydrophthalic anhydride, methylhexahydrophthalic anhydride, hexahydrophthalic anhydride , Methylhymic acid anhydride, trialkyltetrahydrophthalic acid anhydride, methylcyclohexene dicarboxylic acid anhydride, methylcyclohexene tetracarboxylic acid anhydride, ethylene
- modified acid anhydrides include those obtained by modifying the above acid anhydride with glycol.
- glycols that can be used for modification include alkylene glycols such as ethylene glycol, propylene glycol, and neopentyl glycol; polyether glycols such as polyethylene glycol, polypropylene glycol, and pothitetramethylene ether glycol. It is done.
- a copolymer polyether glycol of two or more kinds of these and / or polyether glycol can also be used.
- the modified acid anhydride is preferably modified with 0.4 mol or less of glycol per 1 mol of acid anhydride.
- the modification amount is not more than the above upper limit, the viscosity of the epoxy resin composition does not become too high, the workability tends to be good, and the speed of the curing reaction with the epoxy resin tends to be good. .
- the acid anhydride curing agents mentioned above may be used alone or in any combination and blending ratio.
- use so that the equivalent ratio of the functional group in the curing agent to the epoxy group in all epoxy resin components in the epoxy resin composition is in the range of 0.8 to 1.5. Is preferred. Within this range, unreacted epoxy groups and functional groups of the curing agent are unlikely to remain, which is preferable.
- amide type curing agents include dicyandiamide and its derivatives, and polyamide compounds.
- curing agent may be used only by 1 type, or may be used 2 or more types by arbitrary combinations and compounding ratios.
- the amide-based curing agent is in the range of 0.8 to 1.5 in terms of an equivalent ratio of functional groups in the curing agent to epoxy groups in all epoxy compound epoxy resin components contained in the epoxy compound epoxy resin composition. It is preferable to use as described above. Within this range, unreacted epoxy groups and functional groups of the curing agent are unlikely to remain, which is preferable.
- imidazoles examples include 2-phenylimidazole, 2-ethyl-4 (5) -methylimidazole, 2-phenyl-4-methylimidazole, 1-benzyl-2-methylimidazole, 1-benzyl-2-phenylimidazole.
- the imidazoles listed above may be used alone, or two or more may be used in any combination and mixing ratio.
- the imidazole-based curing agent is in the range of 0.8 to 1.5 in terms of an equivalent ratio of functional groups in the curing agent to epoxy groups in all epoxy compound epoxy resin components contained in the epoxy compound epoxy resin composition. It is preferable to use it. Within this range, unreacted epoxy groups and functional groups of the curing agent are unlikely to remain, which is preferable.
- ⁇ Other curing agents> In the epoxy resin composition of the present invention, other curing agents can be used in addition to the curing agent.
- Other curing agents that can be used in the epoxy resin composition of the present invention are not particularly limited, and any of those generally known as curing agents for epoxy resins can be used. These other curing agents may be used alone or in combination of two or more.
- the epoxy resin composition of the present invention may have a curing accelerator.
- the curing accelerator contained in the epoxy resin composition of the present invention include phosphorus-based curing accelerators, tetraphenyl boron salts, organic acid dihydrazides, and boron halide amine complexes. These curing accelerators may be used alone or in combination of two or more in any combination and blending ratio. Among these, an epoxy resin composition using a phosphorus curing accelerator is particularly preferable because of excellent heat resistance.
- phosphorus-based curing accelerator as the curing accelerator of the epoxy resin composition of the present invention is particularly excellent in heat resistance are not clear, among the phosphorus-based curing accelerators, oxidation that does not contribute to curing is performed.
- the phosphorus-based curing accelerator traps sodium ions in the epoxy resin composition to form a stable complex, and this complex contributes to improving the heat resistance, thereby improving the heat resistance of the resulting cured product. It is thought to do.
- Examples of phosphorus curing accelerators include triphenylphosphine, diphenyl (p-tolyl) phosphine, tris (alkylphenyl) phosphine, tris (alkoxyphenyl) phosphine, tris (alkyl / alkoxyphenyl) phosphine, and tris (dialkylphenyl).
- Phosphine tris (trialkylphenyl) phosphine, tris (tetraalkylphenyl) phosphine, tris (dialkoxyphenyl) phosphine, tris (trialkoxyphenyl) phosphine, tris (tetraalkoxyphenyl) phosphine, trialkylphosphine, dialkylarylphosphine and Organic phosphines such as alkyldiarylphosphine, complexes of these organic phosphines and organic borons, and organic phosphines Maleic anhydride, 1,4-benzoquinone, 2,5-toluquinone, 1,4-naphthoquinone, 2,3-dimethylbenzoquinone, 2,6-dimethylbenzoquinone, 2,3-dimethoxy-5-methyl-1, Examples thereof include quinone compounds such as 4-benzoquinone, 2,3-dimethoxy-1,
- the phosphorus-based curing accelerator is 0.1 weight with respect to 100 parts by weight of an epoxy resin (hereinafter, may be referred to as “total epoxy resin component”) as a solid content contained in the epoxy resin composition of the present invention. It is preferable to use in the range of 20 parts by weight or more and 20 parts by weight or less. More preferably, it is 0.5 parts by weight or more, further preferably 1 part by weight or more, more preferably 15 parts by weight or less, and still more preferably 10 parts by weight or less.
- the content of the phosphorus-based curing accelerator is equal to or more than the lower limit value, it is preferable to obtain a heat resistance improvement effect and a curing acceleration effect by including the phosphorus-based curing accelerator in the epoxy resin composition containing sodium ions. On the other hand, it is preferable that it is not more than the above upper limit value because desired cured properties are easily obtained.
- the phosphorus-based curing accelerator is included in the composition in order to effectively improve the heat resistance by including the phosphorus-based curing accelerator in the epoxy resin composition containing sodium ions. It is preferable to blend such that the P / Na molar ratio is preferably 50 or more and less than 900, particularly preferably 70 or more and less than 200, in terms of phosphorus atom, with respect to sodium ions determined by the method.
- the epoxy resin composition of the present invention can be cured using a phosphorus-based curing accelerator and a curing agent that function as a curing accelerator.
- curing agent and a phosphorus hardening accelerator do not contain a sodium ion normally, it is preferable to use the hardening
- the curing time can be shortened and the curing temperature can be lowered, and a desired cured product can be easily obtained.
- the epoxy resin composition of the present invention may further contain a curing accelerator other than the aforementioned phosphorus-based curing accelerator.
- a curing accelerator other than the phosphorus-based curing accelerator include tetraphenyl boron salts, organic acid dihydrazides, and boron halide amine complexes. These curing accelerators may be used alone or in combination of two or more in any combination and blending ratio.
- the curing accelerator other than the phosphorus-based curing accelerator is preferably based on the total of the phosphorus-based curing accelerator and the curing accelerator other than the phosphorus-based curing accelerator. It is preferable to use 80% by weight or less, particularly preferably 50% by weight or less.
- an inorganic filler in the epoxy resin composition of the present invention, an inorganic filler, a release agent, a coupling agent and the like can be appropriately blended as necessary.
- An inorganic filler can be blended in the epoxy resin composition of the present invention.
- the inorganic filler include fused silica, crystalline silica, glass powder, alumina, calcium carbonate, calcium sulfate, talc, and boron nitride.
- a crushing type and / or spherical, fused and / or crystalline silica powder filler is preferable.
- the thermal expansion coefficient of the semiconductor encapsulant can be made closer to the internal silicon chip or lead frame, and the semiconductor encapsulant can be used. Since the moisture absorption amount of the entire stopper can be reduced, the solder crack resistance can be improved.
- the average particle diameter of the inorganic filler is usually 1 to 50 ⁇ m, preferably 1.5 to 40 ⁇ m, more preferably 2 to 30 ⁇ m.
- the melt viscosity does not become excessively high and fluidity is not easily lowered, and when the average particle size is not more than the upper limit, a narrow gap in the mold is formed during molding. It is preferable because the filler is not easily clogged and the filling property of the material is easily improved.
- the inorganic filler is preferably blended in the range of 60 to 95% by weight of the entire epoxy resin composition.
- the inorganic filler may contain sodium ions as impurities. Therefore, when an inorganic filler is used in the epoxy resin composition of the present invention, it is necessary to consider such an amount of sodium ions.
- a release agent can be blended in the epoxy resin composition of the present invention.
- the release agent include natural waxes such as carnauba wax; synthetic waxes such as polyethylene wax; higher fatty acids such as stearic acid and zinc stearate and metal salts thereof; and hydrocarbon release agents such as paraffin. It can. These may be used alone or in combination of two or more in any combination and blending ratio.
- the amount of the release agent is preferably 0.1 to 5.0 with respect to 100 parts by weight of the total epoxy resin component in the epoxy resin composition. Part by weight, more preferably 0.5 to 3.0 parts by weight. It is preferable for the amount of the release agent to be within the above range because good release properties can be exhibited while maintaining the curing characteristics of the epoxy resin composition.
- a coupling agent is preferably blended in the epoxy resin composition of the present invention.
- the coupling agent is preferably used in combination with an inorganic filler, and the adhesiveness between the matrix epoxy resin and the inorganic filler can be improved by blending the coupling agent.
- Examples of the coupling agent include silane coupling agents and titanate coupling agents.
- silane coupling agent examples include epoxy silanes such as ⁇ -glycidoxypropyltrimethoxysilane, ⁇ -glycidoxypropyltriethoxysilane and ⁇ - (3,4-epoxycyclohexyl) ethyltrimethoxysilane, ⁇ - Aminopropyltriethoxysilane, N- ⁇ (aminoethyl) ⁇ -aminopropyltrimethoxysilane, N- ⁇ (aminoethyl) ⁇ -aminopropylmethyldimethoxysilane, ⁇ -aminopropyltrimethoxysilane and ⁇ -ureidopropyltriethoxy Aminosilanes such as silane, mercaptosilanes such as 3-mercaptopropyltrimethoxysilane, p-styryltrimethoxysilane, vinyltrichlorosilane, vinyltris ( ⁇ -meth
- titanate coupling agents include isopropyl triisostearoyl titanate, isopropyl tri (N-aminoethyl / aminoethyl) titanate, diisopropyl bis (dioctyl phosphate) titanate, tetraisopropyl bis (dioctyl phosphite) titanate, tetraoctyl bis ( Ditridecyl phosphite) titanate, tetra (2,2-diallyloxymethyl-1-butyl) bis (ditridecyl) phosphite titanate, bis (dioctylpyrophosphate) oxyacetate titanate and bis (dioctylpyrophosphate) ethylene titanate It is done.
- These coupling agents may be used alone or in a combination of two or more in any combination and ratio.
- the blending amount thereof is preferably 0.1 to 3.0 parts by weight with respect to 100 parts by weight of all epoxy resin components. If the blending amount of the coupling agent is greater than or equal to the lower limit, the effect of improving the adhesion between the epoxy resin that is the matrix and the inorganic filler due to the blending of the coupling agent tends to be improved. When the blending amount of the agent is not more than the above upper limit value, the coupling agent is less likely to bleed out from the resulting cured product.
- epoxy resin composition of the present invention components other than those described above (may be referred to as “other components” in the present invention) can be blended.
- other components include flame retardants, plasticizers, reactive diluents, pigments, and the like, which can be appropriately blended as necessary.
- the epoxy resin composition of the present invention does not prevent any compounding other than the components listed above.
- Examples of the flame retardant used in the epoxy resin composition of the present invention include halogen flame retardants such as brominated epoxy resins and brominated phenol resins, antimony compounds such as antimony trioxide, red phosphorus, phosphate esters, and phosphines. And the like, phosphorus flame retardants such as nitrogen flame retardants such as melamine derivatives, and inorganic flame retardants such as aluminum hydroxide and magnesium hydroxide.
- halogen flame retardants such as brominated epoxy resins and brominated phenol resins
- antimony compounds such as antimony trioxide, red phosphorus, phosphate esters, and phosphines.
- phosphorus flame retardants such as nitrogen flame retardants such as melamine derivatives
- inorganic flame retardants such as aluminum hydroxide and magnesium hydroxide.
- the cured product of the present invention can be obtained by curing the epoxy resin composition of the present invention.
- the cured product of the present invention has particularly excellent characteristics in heat resistance.
- the method for curing the epoxy resin composition of the present invention is not particularly limited, but usually a cured product can be obtained by a thermosetting reaction by heating. During the thermosetting reaction, it is preferable to select a curing temperature as appropriate depending on the type of curing agent used.
- the curing temperature is usually 130 to 200 ° C.
- the curing temperature can be lowered by adding an accelerator to these curing agents.
- the reaction time is preferably 1 to 20 hours, more preferably 2 to 18 hours, still more preferably 3 to 15 hours. It is preferable for the reaction time to be not less than the lower limit value because the curing reaction tends to proceed sufficiently. On the other hand, it is preferable for the reaction time to be less than or equal to the upper limit value because it is easy to reduce deterioration due to heating and energy loss during heating.
- the epoxy resin and the epoxy resin composition of the present invention provide a cured product having excellent heat resistance, the epoxy resin and the epoxy resin composition can be effectively used for any application as long as these physical properties are required.
- paint fields such as electrodeposition paint for automobiles, heavy duty anti-corrosion paint for ships and bridges, paint for inner surface of beverage cans, laminates, semiconductor encapsulant, resist material, insulating powder paint, coil impregnation, etc.
- bridge seismic reinforcement, concrete reinforcement, building flooring, lining of water supply facilities, drainage / water-permeable pavement, or civil / construction / adhesive fields such as adhesives for vehicles and aircraft It can be used suitably.
- the epoxy resin composition of the present invention may be used after curing for the above application, or may be cured in the production process for the above application.
- the present invention will be described more specifically based on examples, but the present invention is not limited to the following examples.
- the value of various manufacturing conditions and evaluation results in the following examples has a meaning as a preferable value of the upper limit or the lower limit in the embodiment of the present invention, and the preferable range is the above-described upper limit or lower limit value.
- a range defined by a combination of values of the following examples or values of the examples may be used.
- the reaction is completed by maintaining at 65 ° C. for 30 minutes, and the reaction solution is transferred to a 3 L separatory funnel and allowed to stand at 65 ° C. for 1 hour, and then the aqueous layer is extracted from the separated oil layer and aqueous layer. Raw salt and excess sodium hydroxide were removed. Subsequently, excess epichlorohydrin and isopropyl alcohol were distilled off from the product under reduced pressure to obtain a crude epoxy resin.
- This crude epoxy resin was dissolved in 300 g of methyl isobutyl ketone, 4 g of 48.5 wt% sodium hydroxide aqueous solution was added, and reacted again at a temperature of 65 ° C. for 1 hour. Thereafter, 167 g of methyl isobutyl ketone was added, 130 g of water was added, transferred to a 3 L separatory funnel, allowed to stand at 65 ° C. for 1 hour, and then the aqueous layer was extracted from the separated oil layer and aqueous layer. A solution was obtained.
- Table 1 shows the results of measuring the sodium ion content, epoxy equivalent, and melt viscosity at 150 ° C. of the obtained epoxy resins 1, 2, 3, and 4 by the following methods.
- epoxy resins 1, 2, 3 and 4 are all epoxy resins containing 4,4′-bishydroxy-3,3 ′, 5,5′-tetramethylbiphenyl diglycidyl ether.
- n was 0.05.
- Atomic absorption photometer Z-2710, Hitachi High-Tech Science Co., Ltd.
- 0.2 g of sample was dissolved in 10 ml of N-methyl-2-pyrrolidone and measured with an atomic absorption photometer.
- the curing agents and phosphorus curing accelerators used are as follows.
- Curing agent phenol novolak resin (trade name Resitop PSM6200 manufactured by Gunei Chemical Industry Co., Ltd. (hydroxyl equivalent: 103 g / equivalent, softening point: 85 ° C.)
- Phosphorus curing accelerator Triphenylphosphine (trade name, triphenylphosphine, manufactured by Tokyo Chemical Industry Co., Ltd.)
- both the curing agent and the phosphorus-based curing accelerator do not contain sodium ions (the detection limit is less than 1 ppm).
- Table 2 shows the results of testing the obtained cured product for a 0.5% thermogravimetric reduction temperature by the following method as an evaluation of heat resistance.
- ⁇ Heat resistance 0.5% thermal weight loss temperature (° C)> 100 mg of the cured product was scraped, and 10 mg was weighed and sampled to prepare a sample. This sample was subjected to thermal analysis using a thermal analyzer (TG / DTA: EXSTAR 7200 manufactured by Seiko Instruments Inc.) (temperature increase rate: 5 ° C./min, measurement temperature range: 30 ° C. to 350 ° C., air : Flow rate 200 mL / min). The temperature at the time when the weight of the cured product was reduced by 0.5% was measured and set as the 0.5% weight reduction temperature. The higher the 0.5% weight loss temperature, the better the heat resistance.
- TG / DTA EXSTAR 7200 manufactured by Seiko Instruments Inc.
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Abstract
Description
[1]以下の測定方法で求めたナトリウムイオンの含有量が1~12ppmであるテトラメチルビフェノール型エポキシ樹脂。
(測定方法)試料をN-メチルピロリドンに溶解した溶液を用い原子吸光法によって測定する。
[2]エポキシ当量が174~300g/当量の範囲にある[1]に記載のテトラメチルビフェノール型エポキシ樹脂。
[3]150℃の溶融粘度が0.001~10Pa・sの範囲にある[1]又は[2]に記載のテトラメチルビフェノール型エポキシ樹脂。
[4]テトラメチルビフェノール型エポキシ樹脂が、4,4’-ビスヒドロキシ-3,3’,5,5’-テトラメチルビフェニルのジグリシジルエーテルを含む[1]から[3]のいずれか1に記載のテトラメチルビフェノール型エポキシ樹脂。
[5]テトラメチルビフェノール型エポキシ樹脂および硬化剤を含有するエポキシ樹脂組成物であって、以下の測定方法で求めたナトリウムイオンの含有量が0.6~12ppmであるエポキシ樹脂組成物。
(測定方法)試料をN-メチルピロリドンに溶解した溶液を用い原子吸光法によって測定する。
[6]テトラメチルビフェノール型エポキシ樹脂のエポキシ当量が174~300g/当量の範囲にある[5]に記載のエポキシ樹脂組成物。
[7]テトラメチルビフェノール型エポキシ樹脂の150℃の溶融粘度が0.001~10Pa・sの範囲にある[5]又は[6]に記載のエポキシ樹脂組成物。
[8]テトラメチルビフェノール型エポキシ樹脂が、4,4’-ビスヒドロキシ-3,3’,5,5’-テトラメチルビフェニルのジグリシジルエーテルを含む[5]から[7]のいずれか1に記載のエポキシ樹脂組成物。
[9]さらに硬化促進剤を含む[5]から[8]のいずれか1に記載のエポキシ樹脂組成物。
[10]硬化促進剤がリン系硬化促進剤である[9]に記載のエポキシ樹脂組成物。
[11]リン系硬化促進剤の含有量が、エポキシ樹脂組成物中の以下の測定方法で求めたナトリウムイオンに対して、リン原子換算量としてP/Naモル比が50以上、900未満である[10]に記載のエポキシ樹脂組成物。
(測定方法)試料をN-メチルピロリドンに溶解した溶液を用い原子吸光法によって測定する。
[12][5]から[11]のいずれか1に記載のエポキシ樹脂組成物を硬化させた硬化物。
[13][5]から[11]のいずれか1に記載のエポキシ樹脂組成物を含む半導体封止材。
本発明のエポキシ樹脂は、テトラメチルビフェノール型エポキシ樹脂(以下「本発明のエポキシ樹脂」と称することがある)である。本発明のテトラメチルビフェノール型エポキシ樹脂は、通常、一般式(I)で表される。
なお、本発明のエポキシ樹脂は、一般式(I)においてnの値が異なる複数の化合物の混合物であってもよい。また、このような混合物である場合は、一般式(I)におけるnの値が10を超えるエポキシ樹脂が含有することを排除するものではない。
本発明のエポキシ樹脂は、封止材用エポキシ樹脂としての取り扱い性の観点から、エポキシ当量が174g/当量以上であり、300g/当量以下であることが好ましい。より取り扱い性を良好なものとする観点から、エポキシ当量は174g/当量以上であり、200g/当量以下であることがより好ましい。この中でも特に180g/当量以上、190g/当量以下であることが更に好ましい。
なお、本発明において「エポキシ当量」とは、「1当量のエポキシ基を含むエポキシ樹脂の質量」と定義され、JIS K7236(2001年)に準じて測定することができる。
本発明のエポキシ樹脂は、封止材用エポキシ樹脂としての取り扱い性の観点から、150℃の溶融粘度が0.001Pa・s以上であり、10Pa・s以下であることが好ましく、より取り扱い性を良好なものとする観点から、この溶融粘度は、0.001Pa・s以上であり、3Pa・s以下であることがより好ましい。
本発明のテトラメチルビフェノール型エポキシ樹脂の製造方法については特に制限はないが、例えば、以下に説明する一段法による製造方法等が挙げられる。
本発明のエポキシ樹脂組成物は、テトラメチルビフェノール型エポキシ樹脂及び硬化剤を含有するエポキシ樹脂組成物であって、以下の測定方法で求めたナトリウムイオンの含有量が0.6~12ppmである。
(測定方法)試料をN-メチルピロリドンに溶解した溶液を用い原子吸光法によって測定する。
本発明において硬化剤とは、エポキシ樹脂のエポキシ基間の架橋反応及び/又は鎖長延長反応に寄与する物質を示す。なお、本発明においては通常、「硬化促進剤」と呼ばれるものであってもエポキシ樹脂のエポキシ基間の架橋反応及び/又は鎖長延長反応に寄与する物質であれば、硬化剤とみなすこととする。
硬化剤は1種のみで用いても、2種以上を任意の組み合わせ及び配合比率で用いてもよい。硬化剤の2種以上を併用する場合、これらをあらかじめ混合して混合硬化剤を調製してから使用してもよいし、エポキシ樹脂組成物の各成分を混合する際に硬化剤の各成分をそれぞれ別々に添加して同時に混合してもよい。
フェノール系硬化剤としては、例えば、ビスフェノールA、ビスフェノールF、ビスフェノールS、ビスフェノールAD、ハイドロキノン、レゾルシン、メチルレゾルシン、ビフェノール、テトラメチルビフェノール、ジヒドロキシナフタレン、ジヒドロキシジフェニルエーテル、チオジフェノール類、フェノールノボラック樹脂、クレゾールノボラック樹脂、フェノールアラルキル樹脂、ビフェニルアラルキル樹脂、ナフトールアラルキル樹脂、テルペンフェノール樹脂、ジシクロペンタジエンフェノール樹脂、ビスフェノールAノボラック樹脂、トリスフェノールメタン型樹脂、ナフトールノボラック樹脂、臭素化ビスフェノールA及び臭素化フェノールノボラック樹脂等の種々の多価フェノール類や、種々のフェノール類とベンズアルデヒド、ヒドロキシベンズアルデヒド、クロトンアルデヒド及びグリオキザール等の種々のアルデヒド類との縮合反応で得られる多価フェノール樹脂類、キシレン樹脂とフェノール類との縮合反応で得られる多価フェノール樹脂類、重質油又はピッチ類とフェノール類とホルムアルデヒド類との共縮合樹脂並びにフェノール・ベンズアルデヒド・キシリレンジメトキサイド重縮合物、フェノール・ベンズアルデヒド・キシリレンジハライド重縮合物、フェノール・ベンズアルデヒド・4,4’-ジメトキサイドビフェニル重縮合物およびフェノール・ベンズアルデヒド・4,4’-ジハライドビフェニル重縮合物等の各種のフェノール樹脂類等が挙げられる。これらのフェノール系硬化剤は1種のみで用いても、2種以上を任意の組み合わせ及び配合比率で用いてもよい。
アミン系硬化剤としては、例えば、脂肪族アミン類、ポリエーテルアミン類、脂環式アミン類、芳香族アミン類および第3級アミン等が挙げられる。
酸無水物系硬化剤としては、例えば、酸無水物、および酸無水物の変性物等が挙げられる。
アミド系硬化剤としては、例えば、ジシアンジアミド及びその誘導体、並びにポリアミド化合物等が挙げられる。アミド系硬化剤は1種のみで用いても、2種以上を任意の組み合わせ及び配合比率で用いてもよい。前記のアミド系硬化剤は、エポキシ化合物エポキシ樹脂組成物中に含まれる全エポキシ化合物エポキシ樹脂成分中のエポキシ基に対する硬化剤中の官能基の当量比で0.8~1.5の範囲となるように用いることが好ましい。この範囲内であると未反応のエポキシ基や硬化剤の官能基が残留しにくくなるために好ましい。
イミダゾール類としては、例えば、2-フェニルイミダゾール、2-エチル-4(5)-メチルイミダゾール、2-フェニル-4-メチルイミダゾール、1-ベンジル-2-メチルイミダゾール、1-ベンジル-2-フェニルイミダゾール、1-シアノエチル-2-ウンデシルイミダゾール、1-シアノ-2-フェニルイミダゾール、1-シアノエチル-2-ウンデシルイミダゾールトリメリテイト、1-シアノエチル-2-フェニルイミダゾリウムトリメリテイト、2,4-ジアミノ-6-[2’-メチルイミダゾリル-(1’)]-エチル-s-トリアジン、2,4-ジアミノ-6-[2’-エチル-4’-メチルイミダゾリル-(1’)]-エチル-s-トリアジン、2,4-ジアミノ-6-[2’-メチルイミダゾリル-(1’)]-エチル-s-トリアジンイソシアヌル酸付加体、2-フェニルイミダゾールイソシアヌル酸付加体、2-フェニル-4,5-ジヒドロキシメチルイミダゾール、2-フェニル-4-メチル-5-ヒドロキシメチルイミダゾール、及びエポキシ樹脂と前記イミダゾール類との付加体等が挙げられる。なお、イミダゾール類は触媒能を有するため、一般的には硬化促進剤にも分類されうるが、本発明においては硬化剤として分類するものとする。
本発明のエポキシ樹脂組成物においては前記硬化剤以外にその他の硬化剤を用いることができる。本発明のエポキシ樹脂組成物に使用することのできるその他の硬化剤は特に制限はなく、一般的にエポキシ樹脂の硬化剤として知られているものはすべて使用できる。これらの他の硬化剤は1種のみで用いても、2種以上を組み合わせて用いてもよい。
本発明のエポキシ樹脂組成物は硬化促進剤を有していてもよい。本発明のエポキシ樹脂組成物に含有される硬化促進剤としては、リン系硬化促進剤、テトラフェニルボロン塩、有機酸ジヒドラジド及びハロゲン化ホウ素アミン錯体等が挙げられる。これらの硬化促進剤は、1種のみで用いても2種以上を任意の組み合わせ及び配合比率で組み合わせて用いてもよい。これらの中でも、リン系硬化促進剤を用いたエポキシ樹脂組成物が特に耐熱性に優れるため好ましい。
本発明のエポキシ樹脂組成物の硬化促進剤としてリン系硬化促進剤を用いたものが特に耐熱性に優れる理由の詳細は定かではないが、リン系硬化促進剤のうち、硬化に寄与しない酸化したリン系硬化促進剤が、エポキシ樹脂組成物中のナトリウムイオンをトラップして安定な複合体を形成し、この複合体が耐熱性の向上に寄与することにより、得られる硬化物の耐熱性が向上するためと考えられる。
本発明のエポキシ樹脂組成物は、前述のリン系硬化促進剤以外の硬化促進剤を更に含有していてもよい。リン系硬化促進剤以外の硬化促進剤としては、例えば、テトラフェニルボロン塩、有機酸ジヒドラジドおよびハロゲン化ホウ素アミン錯体等が挙げられる。これらの硬化促進剤は、1種のみで用いても2種以上を任意の組み合わせ及び配合比率で組み合わせて用いてもよい。
本発明のエポキシ樹脂組成物には無機充填材を配合することができる。無機充填材としては、例えば、溶融シリカ、結晶性シリカ、ガラス粉、アルミナ、炭酸カルシウム、硫酸カルシウム、タルクおよびチッ化ホウ素等が挙げられる。これらの中でも半導体封止の用途に用いる場合には、破砕型及び/又は球状の、溶融及び/又は結晶性シリカ粉末充填材が好ましい。
本発明のエポキシ樹脂組成物には離型剤を配合することができる。離型剤としては例えば、カルナバワックス等の天然ワックス;ポリエチレンワックス等の合成ワックス;ステアリン酸やステアリン酸亜鉛等の高級脂肪酸類及びその金属塩類;パラフィン等の炭化水素系離型剤を用いることができる。これらは、1種のみで用いても2種以上を任意の組み合わせ及び配合比率で組み合わせて用いてもよい。
本発明のエポキシ樹脂組成物には、カップリング剤を配合することが好ましい。カップリング剤は無機充填材と併用することが好ましく、カップリング剤を配合することにより、マトリックスであるエポキシ樹脂と無機充填材との接着性を向上させることができる。カップリング剤としては、例えば、シランカップリング剤およびチタネートカップリング剤等が挙げられる。
本発明のエポキシ樹脂組成物には、前記した以外の成分(本発明において、「その他の成分」と称することがある。)を配合することができる。その他の成分としては、例えば、難燃剤、可塑剤、反応性希釈剤および顔料等が挙げられ、必要に応じて適宜に配合することができる。ただし、本発明のエポキシ樹脂組成物は上記で挙げた成分以外のものを配合することを何ら妨げるものではない。
本発明のエポキシ樹脂組成物を硬化させることにより、本発明の硬化物を得ることができる。本発明の硬化物は、特に耐熱性において優れた特性を有するものである。
本発明のエポキシ樹脂及びエポキシ樹脂組成物は、耐熱性に優れた硬化物を与えるものであるため、これらの物性が求められる用途であれば、いかなる用途にも有効に用いることができる。
温度計、撹拌装置、冷却管を備えた内容量2Lの四口フラスコにテトラメチルビフェノール[三菱化学(株)製]137g、エピクロルヒドリン627g、イソプロピルアルコール244g、水87gを仕込み、65℃に昇温して均一に溶解させた後、48.5重量%の水酸化ナトリウム水溶液108gを90分かけて滴下した。
装置:原子吸光光度計(株式会社 日立ハイテクサイエンス社製 Z-2710)
試料0.2gをN-メチル-2-ピロリドン10mlに溶解し、原子吸光光度計にて測定。
JIS K7236(2001年)に準じて測定。
装置:コーンプレート粘度計[東海八神(株)製]
150℃に調整した装置の熱板の上にエポキシ樹脂を溶融させ、回転速度750rpmで粘度を測定。
[実施例1~5及び比較例1]
表2に示す割合でエポキシ樹脂と硬化剤を配合し、アルミ皿にて120℃で5分間溶融混練した。その後、リン系硬化促進剤を表2に示す量入れて均一に分散させ、エポキシ樹脂組成物を得た。これを120℃で2時間、次いで175℃で6時間加熱して硬化させ、硬化物を得た。なお、表2中、「部」は「重量部」を表す。
硬化剤:フェノ-ルノボラック樹脂(群栄化学工業社製 商品名 レヂトップ PSM6200(水酸基当量:103g/当量、軟化点:85℃))
リン系硬化促進剤:トリフェニルホスフィン(東京化成工業株式会社製 商品名 トリフェニルホスフィン)
硬化物を100mg削り取り、そこから10mgを計量し、分取してサンプルとした。このサンプルについて、熱分析装置(TG/DTA:セイコーインスツルメント社製 EXSTAR7200)を用いて、熱分析を行った(昇温速度:5℃/分、測定温度範囲:30℃から350℃、空気:流量200mL/分)。硬化物の重量が0.5%減少した時点の温度を測定し0.5%重量減少温度とした。0.5%重量減少温度が高いほど耐熱性に優れるものと評価される。
表1,2に示すように、ナトリウムイオンを所定の割合で含むエポキシ樹脂組成物を用いた実施例1~5の硬化物は、比較例1の硬化物に対し、耐熱性に優れたものであることがわかった。
表3に記載のナトリウム化合物を予め表3記載の添加量になるように前記エポキシ樹脂4に混合した他は、前記比較例1と同様にして、エポキシ樹脂組成物を得た。実施例1~5と同様の方法によって、これらのエポキシ樹脂組成物を硬化し、得られた硬化物の0.5%熱重量減少温度を試験した結果を表3に示す。なお、表3に記載のナトリウム化合物はいずれもN-メチルピロリドンに溶解しなかった。
表3に示すように、ナトリウムを含有させた場合であっても、本測定方法で測定した場合のナトリウムイオン含有量が所定範囲内に入らない場合は、本発明の効果が得られないことがわかった。
Claims (13)
- 以下の測定方法で求めたナトリウムイオンの含有量が1~12ppmであるテトラメチルビフェノール型エポキシ樹脂。
(測定方法)試料をN-メチルピロリドンに溶解した溶液を用い原子吸光法によって測定する。 - エポキシ当量が174~300g/当量の範囲にある請求項1に記載のテトラメチルビフェノール型エポキシ樹脂。
- 150℃の溶融粘度が0.001~10Pa・sの範囲にある請求項1又は2に記載のテトラメチルビフェノール型エポキシ樹脂。
- テトラメチルビフェノール型エポキシ樹脂が、4,4’-ビスヒドロキシ-3,3’,5,5’-テトラメチルビフェニルのジグリシジルエーテルを含む請求項1から3のいずれか1項に記載のテトラメチルビフェノール型エポキシ樹脂。
- テトラメチルビフェノール型エポキシ樹脂および硬化剤を含有するエポキシ樹脂組成物であって、以下の測定方法で求めたナトリウムイオンの含有量が0.6~12ppmであるエポキシ樹脂組成物。
(測定方法)試料をN-メチルピロリドンに溶解した溶液を用い原子吸光法によって測定する。 - テトラメチルビフェノール型エポキシ樹脂のエポキシ当量が174~300g/当量の範囲にある請求項5に記載のエポキシ樹脂組成物。
- テトラメチルビフェノール型エポキシ樹脂の150℃の溶融粘度が0.001~10Pa・sの範囲にある請求項5又は6に記載のエポキシ樹脂組成物。
- テトラメチルビフェノール型エポキシ樹脂が、4,4’-ビスヒドロキシ-3,3’,5,5’-テトラメチルビフェニルのジグリシジルエーテルを含む請求項5から7のいずれか1項に記載のエポキシ樹脂組成物。
- さらに硬化促進剤を含む請求項5から8のいずれか1項に記載のエポキシ樹脂組成物。
- 硬化促進剤がリン系硬化促進剤である請求項9に記載のエポキシ樹脂組成物。
- リン系硬化促進剤の含有量が、エポキシ樹脂組成物中の以下の測定方法で求めたナトリウムイオンに対して、リン原子換算量としてP/Naモル比が50以上、900未満である請求項10に記載のエポキシ樹脂組成物。
(測定方法)試料をN-メチルピロリドンに溶解した溶液を用い原子吸光法によって測定する。 - 請求項5から11のいずれか1項に記載のエポキシ樹脂組成物を硬化させた硬化物。
- 請求項5から11のいずれか1項に記載のエポキシ樹脂組成物を含む半導体封止材。
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108693709A (zh) * | 2017-03-29 | 2018-10-23 | 株式会社田村制作所 | 感光性树脂组合物 |
CN110719926A (zh) * | 2017-06-07 | 2020-01-21 | Dic株式会社 | 环氧树脂、制造方法、环氧树脂组合物及其固化物 |
Families Citing this family (5)
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KR102244206B1 (ko) * | 2017-12-06 | 2021-04-26 | 스미또모 베이크라이트 가부시키가이샤 | 에폭시 수지 조성물 및 전자 장치 |
WO2021187235A1 (ja) * | 2020-03-16 | 2021-09-23 | 三菱ケミカル株式会社 | エポキシ樹脂組成物、硬化物及び電気・電子部品 |
KR20220093980A (ko) | 2020-12-28 | 2022-07-05 | 코오롱인더스트리 주식회사 | 불포화기 함유 수지, 이의 제조방법 및 이를 포함한 조성물 |
KR102473850B1 (ko) * | 2022-06-14 | 2022-12-05 | 주식회사 신아티앤씨 | 테트라메틸비페놀형 에폭시 수지 및 이의 제조방법 |
TW202402865A (zh) * | 2022-06-14 | 2024-01-16 | 南韓商新亚T&C公司 | 四甲基雙酚型環氧樹脂以及其製備方法,四甲基雙酚型環氧樹脂組成物,固化物 |
Citations (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6067475A (ja) * | 1983-09-22 | 1985-04-17 | Mitsubishi Petrochem Co Ltd | ビスヒドロキシビフエニル誘導体系ジエポキシ化合物の精製法 |
JPH03124758A (ja) * | 1989-10-11 | 1991-05-28 | Yuka Shell Epoxy Kk | 半導体封止用エポキシ樹脂組成物 |
JPH03239718A (ja) * | 1990-02-16 | 1991-10-25 | Yuka Shell Epoxy Kk | 半導体封止用エポキシ樹脂組成物 |
JPH0455422A (ja) * | 1990-06-25 | 1992-02-24 | Yuka Shell Epoxy Kk | 半導体封止用エポキシ樹脂組成物 |
JPH04175331A (ja) * | 1990-11-08 | 1992-06-23 | Yuka Shell Epoxy Kk | エポキシ樹脂粉体組成物 |
JPH05136297A (ja) * | 1991-11-14 | 1993-06-01 | Nippon Kayaku Co Ltd | 電子部品封止用樹脂組成物及びその硬化物 |
JPH07247409A (ja) * | 1994-03-10 | 1995-09-26 | Dainippon Ink & Chem Inc | エポキシ樹脂組成物、エポキシ樹脂混合物の製造方法及び半導体封止材料 |
JP2002128861A (ja) * | 2000-10-23 | 2002-05-09 | Japan Epoxy Resin Kk | エポキシ樹脂組成物及びその製法 |
JP2002212268A (ja) * | 2001-01-19 | 2002-07-31 | Japan Epoxy Resin Kk | 半導体封止用エポキシ樹脂組成物 |
JP2003277467A (ja) * | 2003-04-21 | 2003-10-02 | Dainippon Ink & Chem Inc | エポキシ樹脂の製造方法 |
JP2003327554A (ja) * | 2002-05-09 | 2003-11-19 | Mitsubishi Chemicals Corp | 3,3’,5,5’−テトラメチル−4,4’−ビフェノール及びその製造方法 |
JP2004002830A (ja) * | 2002-04-23 | 2004-01-08 | Mitsubishi Chemicals Corp | 3,3’,5,5’−テトラメチル−4,4’−ビフェノール及びその製造方法ならびにエポキシ樹脂組成物の製造方法 |
JP2004315831A (ja) * | 2004-08-13 | 2004-11-11 | Japan Epoxy Resin Kk | エポキシ樹脂組成物の製造方法 |
JP2004315832A (ja) * | 2004-08-13 | 2004-11-11 | Japan Epoxy Resin Kk | エポキシ樹脂結晶化物の製造方法 |
JP2004331988A (ja) * | 2004-08-13 | 2004-11-25 | Japan Epoxy Resin Kk | 半導体封止用硬化性エポキシ樹脂組成物 |
JP2005002351A (ja) * | 2004-08-13 | 2005-01-06 | Japan Epoxy Resin Kk | 半導体封止用硬化性エポキシ樹脂組成物 |
JP2007056089A (ja) * | 2005-08-23 | 2007-03-08 | Japan Epoxy Resin Kk | 精製エポキシ樹脂の製造方法 |
JP2011207932A (ja) * | 2010-03-29 | 2011-10-20 | Mitsubishi Chemicals Corp | エポキシ樹脂及びエポキシ樹脂組成物 |
WO2014073600A1 (ja) * | 2012-11-08 | 2014-05-15 | 日本化薬株式会社 | エポキシ樹脂混合物、エポキシ樹脂組成物およびその硬化物 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5839677A (ja) | 1981-09-02 | 1983-03-08 | Mitsubishi Petrochem Co Ltd | 新規ポリエポキシ化合物 |
US5104604A (en) | 1989-10-05 | 1992-04-14 | Dexter Electronic Materials Div. Of Dexter Corp. | Flame retardant epoxy molding compound, method and encapsulated device method of encapsulating a semiconductor device with a flame retardant epoxy molding compound |
ES2086474T3 (es) | 1990-05-23 | 1996-07-01 | Shell Int Research | Aductos de compuestos fenolicos y terpenos ciclicos y derivados de dichos aductos. |
JPH0586171A (ja) * | 1991-09-27 | 1993-04-06 | Yuka Shell Epoxy Kk | 半導体封止用のエポキシ樹脂組成物 |
JPH0586170A (ja) * | 1991-09-27 | 1993-04-06 | Yuka Shell Epoxy Kk | 半導体封止用エポキシ樹脂組成物 |
JPH1129694A (ja) | 1997-07-09 | 1999-02-02 | Nippon Steel Chem Co Ltd | エポキシ樹脂組成物及びその硬化物 |
JP2002104857A (ja) * | 2000-09-26 | 2002-04-10 | Matsushita Electric Works Ltd | 人造大理石の製造方法 |
JP3712610B2 (ja) | 2000-12-28 | 2005-11-02 | ジャパンエポキシレジン株式会社 | エポキシ樹脂結晶化物、硬化性組成物及び硬化物 |
JP3986445B2 (ja) * | 2003-02-17 | 2007-10-03 | 東都化成株式会社 | 高純度エポキシ樹脂の製造方法およびエポキシ樹脂組成物 |
JP4826301B2 (ja) | 2006-03-15 | 2011-11-30 | 住友ベークライト株式会社 | 潜伏性触媒の製造方法およびエポキシ樹脂組成物 |
JP2008045075A (ja) | 2006-08-21 | 2008-02-28 | Sumitomo Bakelite Co Ltd | 封止用エポキシ樹脂組成物及び電子部品装置 |
CN101724137B (zh) * | 2009-07-13 | 2011-08-31 | 北京石油化工学院 | 含联苯结构环氧树脂的制备方法 |
US8779034B2 (en) | 2009-09-30 | 2014-07-15 | Dow Global Technologies Llc | Epoxy resin compositions |
JP5552089B2 (ja) | 2011-04-21 | 2014-07-16 | 京セラケミカル株式会社 | 封止用樹脂組成物及び半導体装置 |
JP5933954B2 (ja) * | 2011-10-17 | 2016-06-15 | 新日鉄住金化学株式会社 | エポキシ樹脂組成物及び硬化物 |
-
2015
- 2015-12-02 CN CN201580065745.9A patent/CN107001580A/zh active Pending
- 2015-12-02 SG SG11201704514XA patent/SG11201704514XA/en unknown
- 2015-12-02 WO PCT/JP2015/083939 patent/WO2016088815A1/ja active Application Filing
- 2015-12-02 CN CN201910795156.6A patent/CN110483741B/zh active Active
- 2015-12-02 MY MYPI2017702006A patent/MY181374A/en unknown
- 2015-12-02 JP JP2015235746A patent/JP6607009B2/ja active Active
- 2015-12-02 KR KR1020177015251A patent/KR102466597B1/ko active IP Right Grant
- 2015-12-04 TW TW104140767A patent/TWI739731B/zh active
-
2017
- 2017-06-02 US US15/612,609 patent/US10381282B2/en active Active
Patent Citations (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6067475A (ja) * | 1983-09-22 | 1985-04-17 | Mitsubishi Petrochem Co Ltd | ビスヒドロキシビフエニル誘導体系ジエポキシ化合物の精製法 |
JPH03124758A (ja) * | 1989-10-11 | 1991-05-28 | Yuka Shell Epoxy Kk | 半導体封止用エポキシ樹脂組成物 |
JPH03239718A (ja) * | 1990-02-16 | 1991-10-25 | Yuka Shell Epoxy Kk | 半導体封止用エポキシ樹脂組成物 |
JPH0455422A (ja) * | 1990-06-25 | 1992-02-24 | Yuka Shell Epoxy Kk | 半導体封止用エポキシ樹脂組成物 |
JPH04175331A (ja) * | 1990-11-08 | 1992-06-23 | Yuka Shell Epoxy Kk | エポキシ樹脂粉体組成物 |
JPH05136297A (ja) * | 1991-11-14 | 1993-06-01 | Nippon Kayaku Co Ltd | 電子部品封止用樹脂組成物及びその硬化物 |
JPH07247409A (ja) * | 1994-03-10 | 1995-09-26 | Dainippon Ink & Chem Inc | エポキシ樹脂組成物、エポキシ樹脂混合物の製造方法及び半導体封止材料 |
JP2002128861A (ja) * | 2000-10-23 | 2002-05-09 | Japan Epoxy Resin Kk | エポキシ樹脂組成物及びその製法 |
JP2002212268A (ja) * | 2001-01-19 | 2002-07-31 | Japan Epoxy Resin Kk | 半導体封止用エポキシ樹脂組成物 |
JP2004002830A (ja) * | 2002-04-23 | 2004-01-08 | Mitsubishi Chemicals Corp | 3,3’,5,5’−テトラメチル−4,4’−ビフェノール及びその製造方法ならびにエポキシ樹脂組成物の製造方法 |
JP2003327554A (ja) * | 2002-05-09 | 2003-11-19 | Mitsubishi Chemicals Corp | 3,3’,5,5’−テトラメチル−4,4’−ビフェノール及びその製造方法 |
JP2003277467A (ja) * | 2003-04-21 | 2003-10-02 | Dainippon Ink & Chem Inc | エポキシ樹脂の製造方法 |
JP2004315831A (ja) * | 2004-08-13 | 2004-11-11 | Japan Epoxy Resin Kk | エポキシ樹脂組成物の製造方法 |
JP2004315832A (ja) * | 2004-08-13 | 2004-11-11 | Japan Epoxy Resin Kk | エポキシ樹脂結晶化物の製造方法 |
JP2004331988A (ja) * | 2004-08-13 | 2004-11-25 | Japan Epoxy Resin Kk | 半導体封止用硬化性エポキシ樹脂組成物 |
JP2005002351A (ja) * | 2004-08-13 | 2005-01-06 | Japan Epoxy Resin Kk | 半導体封止用硬化性エポキシ樹脂組成物 |
JP2007056089A (ja) * | 2005-08-23 | 2007-03-08 | Japan Epoxy Resin Kk | 精製エポキシ樹脂の製造方法 |
JP2011207932A (ja) * | 2010-03-29 | 2011-10-20 | Mitsubishi Chemicals Corp | エポキシ樹脂及びエポキシ樹脂組成物 |
WO2014073600A1 (ja) * | 2012-11-08 | 2014-05-15 | 日本化薬株式会社 | エポキシ樹脂混合物、エポキシ樹脂組成物およびその硬化物 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108693709A (zh) * | 2017-03-29 | 2018-10-23 | 株式会社田村制作所 | 感光性树脂组合物 |
CN110719926A (zh) * | 2017-06-07 | 2020-01-21 | Dic株式会社 | 环氧树脂、制造方法、环氧树脂组合物及其固化物 |
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KR20170091622A (ko) | 2017-08-09 |
TWI739731B (zh) | 2021-09-21 |
US10381282B2 (en) | 2019-08-13 |
TW201627393A (zh) | 2016-08-01 |
US20170271226A1 (en) | 2017-09-21 |
CN110483741A (zh) | 2019-11-22 |
JP2016108562A (ja) | 2016-06-20 |
MY181374A (en) | 2020-12-21 |
SG11201704514XA (en) | 2017-07-28 |
JP6607009B2 (ja) | 2019-11-20 |
CN107001580A (zh) | 2017-08-01 |
KR102466597B1 (ko) | 2022-11-11 |
CN110483741B (zh) | 2022-07-12 |
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