CN103501647A - Fiber for artificial hair, and hairpiece product - Google Patents
Fiber for artificial hair, and hairpiece product Download PDFInfo
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- CN103501647A CN103501647A CN201280021528.6A CN201280021528A CN103501647A CN 103501647 A CN103501647 A CN 103501647A CN 201280021528 A CN201280021528 A CN 201280021528A CN 103501647 A CN103501647 A CN 103501647A
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- fiber
- artificial hair
- elastic modulus
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- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41G—ARTIFICIAL FLOWERS; WIGS; MASKS; FEATHERS
- A41G3/00—Wigs
- A41G3/0083—Filaments for making wigs
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- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41G—ARTIFICIAL FLOWERS; WIGS; MASKS; FEATHERS
- A41G3/00—Wigs
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/62—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyesters
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Artificial Filaments (AREA)
- Materials For Medical Uses (AREA)
Abstract
Provided is artificial hair with excellent curling properties. Fiber for artificial hair is generally shaped in a temperature range of 90-150 DEG C. Artificial hair fiber for which the ratio of the storage elastic modulus E' in the shaping temperature region, that is, the ratio E'90/E'150 of the storage elastic modulus at 90 DEG C, E'90, to the storage elastic modulus at 150 DEG C, E'150, is a value of 3-20 maintains mechanical properties to the extent that melting does not occur while deforming adequately to form curls. Since shaping such as curling can be freely performed, hairpiece products that meet consumers' fashion needs are provided.
Description
Technical field
The hair product that the present invention relates to a kind of fiber for artificial hair and use this fiber.
Background technology
Use the artificial hair of synthetic fibers system on the hair product of wig or hair net etc. always.Artificial hair is straight hair mostly, and still, artificial hair is more and more extensive for the situation of fashion in recent years, therefore, and the fiber that requires a kind of artificial hair of doing the processing such as curling to use.
As the fiber for artificial hair with excellent crimp fixing, flame-retardant polyester artificial hair (with reference to patent documentation 1) is for example arranged.The heat resistance of this fiber for artificial hair is high, therefore, can use curler etc. to carry out high-temperature heating, has excellent crimpiness.
But the producer of hair product is for fear of fire damage, be mostly use than curler etc. more 90~150 ℃ of low temperature carry out stample fiber, and anti-flammability fiber for artificial hair as above has and can't fully carry out the problem of stample fiber.
Patent documentation 1: Japanese documentation JP 2009-235626 communique
Summary of the invention
Therefore, main purpose of the present invention is to provide a kind of high fiber for artificial hair of processability of curling grade.
The invention provides the goods of a kind of fiber for artificial hair and use fiber for artificial hair, in the storage elastic modulus E ' with respect to temperature, the storage elastic modulus E ' 90 in the time of 90 ℃ and the ratio E ' 90/E ' 150 of the storage elastic modulus E ' 150 in the time of 150 ℃ are 3~20.
The curve of the described E ' of the storage elastic modulus with respect to temperature has: above-mentioned storage elastic modulus E ' is held certain vitreousness zone; Take and temperature is maximum transition region higher than above-mentioned vitreousness zone and rate of change.Especially, the temperature coordinate of the crossing intersection point of the tangent line of the described storage elastic modulus E ' curve by described vitreousness zone and the tangent line of described storage elastic modulus E ' curve by described transition region is positioned at 180~240 ℃.
Particularly, above-mentioned fiber for artificial hair, it is by take the resin combination manufacturing that the thermoplastic resin of any one or both in mylar and polyamide is principal component.
More preferably, its for from the nozzle bore melting sprays described resin combination and manufactures undrawn yarn, the fiber for artificial hair that described undrawn yarn carried out to manufacturing after stretch processing, there is following characteristics, that is: be ejected into from melting that to manufacture the ratio D1/D2 of the multiplying power D1 be elongated and the multiplying power D2 that carries out being stretched during stretch processing during undrawn yarn be 1.5~14.0.
The present invention also provides a kind of hair product that uses above-mentioned fiber for artificial hair to manufacture.
The invention effect
According to the present invention, can provide the fiber for artificial hair that processability is high.
The accompanying drawing explanation
Fig. 1 means the curve map of relation between storage elastic modulus and temperature.
Fig. 2 means the viscoelastic curve map of the fiber for artificial hair of embodiment.
Fig. 3 means the viscoelastic curve map of the fiber for artificial hair of comparative example.
The specific embodiment
Below, for the present invention, be elaborated, but the present invention is not limited to each embodiment shown below.
The invention provides the there is excellent crimpiness fiber for artificial hair of (formative nature, shape stability).The not special restriction of fiber for artificial hair, such as can be by the resulting synthetic fibers of spinning resin combination or making inorganic agent etc. be attached to the fibrous matter formed on synthetic fibers.
Can form processing by the processor of the producer of fiber for artificial hair, hair product or any one of ultimate consumer of buying hair product.For example, fiber for artificial hair or the producer of hair product apply the shaping processing of curling grade before selling market to fiber for artificial hair.Before fiber for artificial hair is processed into to hair product, the processing of being processed into hair product midway or any one stage of being processed into after hair product can form processing.In addition, the processing that is shaped is not defined as curling (wave), comprises the situation that wave is processed into to straight (straight hair) yet.
Manufacturing process has no particular limits, and the method for heating apparatus contact (pressing) fiber for artificial hair that makes curler etc., the method be exposed to hot blast under the state that fiber for artificial hair is wrapped with to volume core (metal-made cylinder etc.) in is arranged or heat method etc. of its volume core itself.But, generally speaking, be to use the method that fiber for artificial hair is wrapped with to the volume core and places it in heating in heating furnace (baking oven).
The not special restriction of the heating-up temperature of shaping use (forming temperature), can carry out suitable change according to the raw material of fiber for artificial hair etc.But, generally speaking, the scope that this heating-up temperature is 90~150 ℃ (forming temperature zone).
Fig. 1 is the ideograph of the viscoelastic properties for fiber for artificial hair is described.Synthetic fibers can make storage elastic modulus E ' and loss elastic modulus E by heating " descend simultaneously, its rate of change is larger, and the distortion of curling grade is just easier.Therefore, when carrying out the forming temperature zone (the curling temperature province of the baking oven of Fig. 1) of curling grade, rate of change the greater is applicable to fiber for artificial hair.
The change curve of the elastic modelling quantity that the symbol c of Fig. 1 is commercially available heat-resisting artificial hair (E ', E ").Heat-resisting artificial hair is because having heat resistance, and therefore the variation of the elastic modelling quantity under forming temperature (E ', E ") is little, and the formability of curling grade is poor.As shown in symbol a, the b of Fig. 1, when the variation of the elastic modelling quantity under forming temperature (E ', E ") is larger, easily distortion under forming temperature, formability is better.
The variation of the elastic modelling quantity under forming temperature (E ', E ") can be adjusted by changing as the composition of the resin combination of fiber for artificial hair raw material.For example, if take the lower thermoplastic resin of glass transformation temperature is main material, can makes elastic modelling quantity under forming temperature (E ', E ") significantly change, but can make its heat resistance deteriorated.
After shaping processing (city after sale), the ultimate consumer carries out the processing (postforming) of hair product sometimes according to individual hobby.Mostly use commercially available heating apparatus (curler etc.) in postforming, its heating-up temperature is various, be 60~240 ℃.But, because the consumer likes powerful formative nature at short notice, therefore, have and use the pre-sales shaping than city to process the more tendency of high temperature (180~240 ℃, the postforming temperature province).
As shown in curve b, even the rate of change under the forming temperature zone is large, if but arrive postforming temperature province (the curling temperature province of the flatiron of Fig. 1) and start before to have the melting deformation of fiber, can cannot stand the high temperature process of curler, cause sometimes that fiber significantly shrinks, damage of fiber, fracture etc.
Therefore, desirable: as shown in curve a, can melting and larger with the rate of change under the postforming temperature province in the forming temperature zone before arriving the postforming temperature province.Yet the variation of elastic modelling quantity (E ', E ") is also larger when melting, a of Fig. 1, c melting under the postforming temperature province, and b melting before arriving the postforming temperature province.On general the use, can not heat fiber for artificial hair under the high temperature in rear heating-up temperature zone, therefore, if rate of change is larger under the postforming temperature province, as shown in a, c, also it doesn't matter to cause melting under this zone.
The zone that the forming temperature often used in the artificial hair field is 90~150 ℃, and the zone that the postforming temperature of consumer's hobby is 180~240 ℃.That is, elastic modelling quantity has larger variation person for good in these zones.
Though the variation of elastic modelling quantity is better to crimpiness more greatly, excessive variation means the contraction of fiber.For example, with respect to temperature (℃) storage elastic modulus E ' in, storage elastic modulus E ' in the time of 90 ℃ 90 and the ratio E ' 90/E ' 150 of storage elastic modulus E ' 150 in the time of 150 ℃ take 3~20 as good, more preferably 4~10.
Once E ' 90/E ' 150 is less than 3, the variation of the elastic modelling quantity when forming temperature zone (90~150 ℃) will be less, and therefore, curling shaping is difficulty comparatively, causes crimpiness bad.On the other hand, E ' 90/E ' is once 150 surpass 20, and fiber can shrink, thereby causes crimpiness bad.In addition, it would be desirable, E ' 90/E ' 150 is 4~10 o'clock, and fiber can not shrink, and can realize excellent crimpiness.
In addition, consider postforming, though heat resistance the higher person is good, once heat resistance is too high, can't carry out postforming (pressing curling).Therefore, it is desirable to, the deformation temperature of the vitreousness disintegration of crystallization is enclosed should be in the scope of 180~240 ℃.As for deformation temperature, for example, in the tangent line of storage elastic modulus curve, the tangent line that is certain zone (vitreousness zone) by storage elastic modulus, with by temperature higher than the rate of change of this zone and storage elastic modulus the temperature for the position of intersecting point of the tangent line of the highest transition region (or the rate of change of storage elastic modulus is maximum transition point), be considered to this deformation temperature.
By suitably adjusting creating conditions and the composition of raw material of fiber for example, can produce and meet said temperature, viscoelastic fiber for artificial hair.
<resin combination >
Resin combination is to using thermoplastic resin as principal component (more than content 50 quality %), optionally can comprise the additive of fire retardant, filler, colouring agent, antioxidant etc.Viscoplasticity (E ', E " etc.) can be adjusted according to the blending ratio of the thermoplastic resin such as two or more or the mixed proportion of thermoplastic resin and additive (fire retardant, filler etc.).Especially, can, by sneaking into the two or more thermoplastic resins with different glass transition temperature, can obtain being with the postforming temperature province fiber for artificial hair that Flexible change is large in the forming temperature zone.
Except said method, also can create conditions to adjust viscoplasticity by what adjust fiber.For example, can adjust viscoplasticity by suitably changing tractive multiplying power and stretching ratio.In addition, so-called tractive multiplying power, be that resin out is to the multiplying power be stretched till cooling from nozzle bore, and so-called stretching ratio is the multiplying power (multiplying power during stretching) that undrawn yarn is stretched.
Below for tractive multiplying power and stretching ratio, be elaborated.In the manufacturing process of fiber for artificial hair, the composition that will contain thermoplastic resin carries out heating and melting and from the nozzle bore ejection, optionally make it by cartridge heater after the cooling undrawn yarn that obtains.After the nozzle bore ejection, become undrawn yarn until cooling, the multiplying power be stretched is the tractive multiplying power.In addition, the multiplying power be stretched can be by the draw rate of undrawn yarn and recently calculating from the spouting velocity of nozzle.
Then carry out the stretch processing of undrawn yarn, to improve the hot strength of fiber.Stretch processing is by still cooling undrawn yarn, with heating and melting temperature low temperature when spinning heat the operation of on one side carrying out stretching on one side.Undrawn yarn (before adding hot-stretch) is until the multiplying power that stretch processing is stretched is stretching ratio.The multiplying power that is stretched now can be calculated by the ratio of the speed of rolling of silk after the development rate of undrawn yarn and stretch processing.
<thermoplastic resin >
Thermoplastic resin has no particular limits, and can use vinyl chloride resin, acrylic resin, acrylic resin, polylactic resin, mylar, polyamide etc.But, once only use the low resins of heat resistance such as vinyl chloride resin,, under the postforming of high temperature (more than 180 ℃), fiber can produce fire damage, therefore, it is desirable to use or use simultaneously separately the heat-resistant resin of polyamide, mylar etc.
In these resins, the polyester fiber that the present invention should use at aspects such as processability and intensity is especially excellent, the polyamide-based fiber that the polyamide of take is main component and the mylar of take are main component.
Preferably, polyamide-based fiber, polyester fiber are the formed fibers of composition obtained by the phosphorus system of the polyamide Trees fat (or mylar of 100 weight portions) of 100 weight portions and 5~30 weight portions or bromide fire retardant melting mixing.Now, by resin and the phosphorus system of regulation ratio or the combination of bromide fire retardant, can significantly improve anti-flammability.
The kind of the polyamide used in polyamide-based fiber has no particular limits, and preferably, for example is selected from nylon 6, nylon 66, and nylon 46, nylon 12, at least one resin in NYLON610 and nylon 612, more preferably select nylon 66.While using nylon 66, sense of touch is good especially.The weight average molecular weight of polyamide (Mw) is the arbitrary value in 10,000~200,000 scopes for example, more particularly, can be 10,000,20,000,40,000,60,000,80,000,100,000,150,000,200,000.
The kind of the mylar used in polyester fiber has no particular limits, PETG, polyphenylene oxide, PETG, polybutylene terephthalate (PBT) etc. are arranged, wherein, at aspects such as heat resistances, PETG is most suitable.
The kind of above-mentioned phosphorus flame retardant also has no particular limits, so long as phosphorus flame retardant commonly used all can be used.As concrete example, can enumerate phosphate based compound, phosphonic acids based compound, phosphinic acids based compound, phosphine oxide based compound, phosphite ester based compound, phosphonate ester based compound, phosphine based compound etc.These compounds can be used alone wherein a kind of, also can two or morely use together.
In addition, above-mentioned bromide fire retardant is not particularly limited, so long as bromide fire retardant commonly used all can be used.As concrete example, can enumerate pentabromotoluene, HBB, decabromodiphenyl, deca-BDE, two (tribromophenoxy) ethane, tetrabromophthalic anhydride, ethylenebis (tetrabromo phthalimide), ethylenebis (penta-bromophenyl), eight trimethylammonium bromide phenyl indans, the brominated phosphate flame retardants such as three (tribromo neopentyl) phosphate, the brominated Polystyrene flame retardant, bromination polypropylene acid benzyl ester flame retardant, the brominated epoxy flame retardant, bromination phenoxy group flame retardant, the brominated polycarbonate flame retardant, tetrabromobisphenol A, tetrabromobisphenol A-bis-(2, 3-dibromopropyl ether), tetrabromobisphenol A-bis-(allyl ether), tetrabromobisphenol A-bis-(hydroxyethyl ether), the tetrabromobisphenol A derivative, the brominated triazine based compounds such as three (tribromophenoxy) triazine, three (2, the 3-dibromo phenyl) brominated tribromo isocyanic acid based compound such as isocyanuric acid ester etc.These can use a kind of, also can two or more mix use.
The ratio that the content of above-mentioned phosphorus system or bromide fire retardant is the polyamide (or mylar of 100 weight portions) with respect to 100 weight portions is 5~30 weight portions, preferably 5~20 weight portions.As long as in this scope, just can guarantee sufficient anti-flammability and avoid the deteriorated of various physical property.
Further, also can contain the particulate that the ratio of the polyamide (or mylar of 100 weight portions) with respect to 100 weight portions is 0.1~5 weight portion.Once the particulate that contains this ratio, concavo-convex gloss and the light of regulating fiber surface that can form by fiber surface, and strengthen the surface area of fiber surface, can the be improved hygroscopic peculiar effect of fiber of result.With respect to the polyamide (or mylar of 100 weight portions) of 100 weight portions, atomic ratio is preferably 0.2~3 weight portion, and what be more preferably is 0.2~2 weight portion.Under this ratio, above-mentioned effect is obvious especially.
Above-mentioned atomic average grain diameter is preferably 0.1~15 μ m, and that be more preferably is 0.2~10 μ m, further 0.5~8 μ m preferably.As long as in this scope, the regulating effect of gloss and light is very large, and, due to atomic interpolation, is difficult for occurring the reduction of fibre strength.
Above-mentioned particulate can be organic particle or inorganic fine particles, can be also to comprise organic particle and inorganic fine particles.So long as get final product with respect to polyamide or the immiscible organic particle of mylar at least a portion, for example, the particle formed by crosslinked acrylic resin or crosslinked polyester resin.
Above-mentioned crosslinked acrylic resin by making acrylic monomer and crosslinking agent carry out dispersion in water, crosslinking curing obtains.Monomer as the acrylic acid series that used here, can enumerate acrylic acid, acrylic acid derivative, for example, methyl acrylate, butyl acrylate, Hexyl 2-propenoate, cyclohexyl acrylate, hydroxy-ethyl acrylate, acrylonitrile, acrylamide, N hydroxymethyl acrylamide, or methacrylic acid, the derivative of methacrylic acid, methyl methacrylate for example, butyl methacrylate, hexyl methacrylate, GMA, Jia base Bing Xi Suan Benzyl ester, the methacrylic acid cyclohexyl ester, the methacrylic acid NVP, methacrylonitrile, Methacrylamide, N hydroxymethyl acrylamide, hydroxyethyl 2-methacrylic acid etc. has the vinyl monomer of a vinyl in a molecule.These can use a kind of, also can two or more mix use.
Above-mentioned cross-linked polyester by making unsaturated polyester (UP) and vinyl monomer carry out dispersion in water, crosslinking curing obtains.Unsaturated polyester (UP) as using here, have no particular limits, and can enumerate and for example make α, beta-unsaturated carboxylic acid or itself and the mixture of saturated acid and the polymer of dihydroxylic alcohols or trihydroxylic alcohol polymerization etc.As unsaturated acids, can enumerate such as fumaric acid, maleic acid, itaconic acid etc., as saturated acid, can enumerate such as phthalic acid, terephthalic acid (TPA), butanedioic acid, glutaric acid, tetrahydrophthalic acid, adipic acid and decanedioic acid etc.In addition, as dihydroxylic alcohols and trihydroxylic alcohol, can enumerate for example ethylene glycol, diethylene glycol (DEG), propane diols, neopentyl glycol, 1,3-PD, 1,6-hexylene glycol, trimethylolpropane etc.On the other hand, as vinyl monomer, have no particular limits, can enumerate such as styrene, chlorostyrene, vinyltoluene, divinylbenzene, acrylic acid, methyl acrylate, acrylonitrile, ethyl acrylate and diallyl phthalate etc.
In addition, as above-mentioned crosslinking agent, so long as there is the monomer of two or more vinyl in a molecule, get final product, comparatively preferably in a molecule, there are two vinyl.As the better monomer of crosslinking agent, for example have divinylbenzene, methacrylic acid and ethylene glycol or with acrylic acid product, such as ethylene glycol dimethacrylate, neopentylglycol dimethacrylate etc., but be not limited to these.The addition of crosslinking agent is preferably 0.02~5 weight portion with respect to the described acrylic monomer of 100 weight portions.As polymerization initiator, preferably peroxidating system radical polymerization initiator, can enumerate such as benzoyl peroxide, benzylhydroperoxide-2-Octyl Nitrite, di-t-butyl peroxide, hydrogen phosphide cumene, methyl ethyl ketone peroxide etc.Radical polymerization initiator is preferably 0.05~10 weight portion with respect to the described acrylic monomer of 100 weight portions.
In addition, as above-mentioned inorganic fine particles, consider the transparency and the impact on developing the color on fiber, preferably its refractive index is the material with the refractive index that approaches polyamide and/or phosphonium flame retardant, can enumerate such as calcium carbonate, oxidation silicon, titanium oxide, aluminium oxide, zinc oxide, talcum, kaolin, montmorillonite, bentonite, mica etc.
In addition, except above-mentioned particulate and fire retardant, also can contain fire retardant, antiheat agent, light stabilizer, fluorescer, antioxidant, antistatic additive, plasticizer, lubricating oil, thermoplastic resin resin in addition etc.Colouring agent by containing pigment etc., can obtain painted in advance fiber (being coloured fibre).
<manufacturing process >
One example of the manufacturing process of synthetic fibers below is described, but the present invention is not limited thereto.
In the thermoplastic resin of polyamide, mylar etc., by the additive of above-mentioned fire retardant and particle etc. in desirable ratio after the universe in advance is mixed, use mixing roll to carry out melting mixing.As the device for melting mixing, can use various general mixing roll.As melting mixing, such as single screw extrusion machine, double screw extruder, roller, Banbury, kneader etc.Wherein, by the adjustment of mixing degree, the simplicity of operation, preferably double screw extruder.Can carry out melt spinning by melt spinning method by the mixing thing that melting mixing is obtained manufactures.
Melt spinning is that the Temperature Setting such as the melt spinning device by extruder, gear pump, spinning head etc. is 270~310 ℃ and carries out melt spinning, make to spin strand by being cooled to below glass transition point after cartridge heater, the speed of dividing by 50~5000m/ is extracted and is obtained spinning silk.In addition, also can put into cooling water and carry out coolingly spinning strand, carry out the control of fiber number.The temperature of the temperature of the temperature of cartridge heater and length, cooling tower and spray amount, bosh, cool time, extraction rate can carry out suitable adjustment by the hole count of spray volume and spinning head.
During melt spinning, use the spinning-nozzle that nozzle bore is special shape, the cross sectional shape of fiber for artificial hair can be set as to the abnormity such as cocoon type, Y type, H type, X-type.
The undrawn yarn obtained is carried out to the hot-stretch processing, to improve the hot strength of fiber.Hot-stretch process can first undrawn yarn temporarily be rolled into after bobbin to stretched this two-step method or non-involvement to bobbin in the operation different from the melt spinning operation and from the melt spinning operation continuously elongated direct spinning stretching method.In addition, hot-stretch is processed and can be adopted a step extension method that once reaches required stretching ratio or the multistep extension method that reaches required stretching ratio by twice above stretching to carry out.Heater as in hot-stretch is processed, can use warm-up mill, hot plate, steam injection equipment, warm water tank etc., also can suitably use these heaters simultaneously.
The fiber number of synthetic fibers is 30~80dtex, 35~75dtex preferably, and this is than being more suitable for artificial hair.In synthetic fibers, the fiber that polyamide-based fiber is non-crimping raw silk shape, its fiber number is generally 10~100dtex, preferably 30~80dtex, more preferably 35~75dtex.
<post processing >
The synthetic fibers that produce can directly be used as fiber for artificial hair, also can be coated with the inorganic agent that contains the oil solvents such as silica gel with the improvement sense of touch etc.The coating of inorganic agent can be before being processed into hair product by synthetic fibers, processing is carried out midway or in any stage after processing, and the operation of being processed into hair product midway be coated on workability, evenly the aspects such as coating are more suitable for.
Fiber for artificial hair can be separately for hair product (head decoration product), also can be mixed together with human hair or other artificial hair.Hair product is hair net (wig), sends out the hair of sheet, pigtail, sending and receiving, doll etc., and the purposes of fiber for artificial hair has no particular limits.In addition, except hair product, also can be for artificial beard, false eyelashes, artificial brow etc.
Embodiment
Below, will utilize embodiment to further describe the present invention, but the present invention is not limited to these embodiment.
<manufacturing process >
Below, the manufacture method of the fiber for hair use bundle of embodiment is described.Polyamide-based fiber (or polyester fiber) is manufactured in the following ways.At first, drying is as polyamide (or mylar), phosphorus system or bromide fire retardant and the particulate of raw material, so that its amount of moisture contained is below 100ppm respectively.
Use following raw material.
Nylon 6: Ube Industries, Ltd, 1013B
Nylon 6,6: Dongli Ltd., CM3001 ?N
Phosphorus flame retardant: Daihachi Chemical Industry Co., Ltd., PX-200
Bromide fire retardant: Albemarle Amada Co., Ltd., HP-7010
Particulate: crosslink propylene acid particles, average grain diameter 1.8 μ m, Soken Chemical & Engineering Co., Ltd.
Polyester (PET): Mitsubishi chemical Co., Ltd, BK ?2180
Batching (mass ratio) is as shown in table 1 below.
[table 1]
Then, the painted of ormal weight added in dry raw material with particle, carry out the universe by each mixed species as shown in table 1, mixed proportion and mix.Carry out melting mixing with the temperature of 280 ℃ after the universe is mixed.Then, mixing thing is configured as to the shaping particles body.Use double screw extruder to carry out melting mixing and shaping particles.
Above-mentioned shaping particles body is dried to and contains moisture lower than after below 100ppm, use melt spinning machine that dried particles is configured as to undrawn yarn.More specifically, the cross section of the nozzle bore of the spinning nozzle in melt spinning machine is rounded, and nozzle bore is 0.5mm.By this melt spinning machine, under the state that is 280 ℃ at Temperature Setting, from the molten polymer of said nozzle hole ejection shaping particles body.Then, the molten polymer of ejection is used that to be positioned under spinning head the water-bath layer of 50 ℃ of 30mm cooling and roll, and obtains undrawn yarn.Adjust the tractive multiplying power by the speed of rolling that changes undrawn yarn.
Then, resulting undrawn yarn being drawn into to 4 times heat-treats afterwards.Then, the speed of dividing with 30m/ is rolled, the fiber that to obtain take polyamide (or polyester) be main body.In the wire drawing and heat treatment of above-mentioned undrawn yarn, use respectively the hot-rolling with 85 ℃ and 200 ℃ heating.Whereby, obtain the fiber of embodiment 1~4 and comparative example 1~2.In addition, adjust stretching ratio by the development rate that changes undrawn yarn.
Fiber for embodiment 1~4, comparative example 1~2 has carried out following evaluation test.
<baking oven crimpiness >
About the baking oven crimpiness, be that fibre bundle 2 grams that the fiber of long 50cm is done up are wrapped with the aluminum cylinder of diameter 20mm fixing two ends, the air circulating type baking oven that drops into 100 ℃ heats 30 minutes.Then, at the thermostatic chamber of 23 ℃ of temperature, relative humidity 50%, aluminum barrel (being wrapped with under the state of fiber) is placed 24 hours.After this, from stainless steel cylinder, take off fibre bundle, fix an end and hang.Now, with the length till from the fibre bundle root to front end, divided by the value of the total length curling (50cm), estimated.Be worth less expression more curling.Be evaluated as following benchmark, take good and good is acceptance value.
Good: value is less than 0.75
Good: value is more than 0.75 and is less than 0.85
Bad: value is more than 0.85
<processability >
About processability, be the frequency of investigation fiber fracture of wire in manufacturing process's (spinning, stretching), by following benchmark, estimated.Take good and good is acceptance value.
Good: as there is no fracture of wire
Good: the fracture of wire of left and right once in 30 minutes, but no problem on the quality of goods
Bad: fracture of wire too much causes manufactures difficulty
<physical property >
According to JIS-L1069 is random, select 10 fibers to carry out tension test, and obtain mean value.With 23 ℃ of test temperatures, relative humidity 50%, draw speed 200mm/min, space length (chuck distance) 200mm, carry out.Hot strength (cN/dtex) is good below 2.0 more than 1.0; Hot strength (cN/dtex) is good below 3.0 more than 0.5; Hot strength (cN/dtex) is less than 0.5 or surpass 3.0 for bad.
<dynamic viscoelastic >
Condition determination with frequency 1.0Hz, 30 ℃ of temperature of beginning, 260 ℃ of end temps, 2 ℃/minutes of programming rates is measured dynamic viscoelastic (tensile modulus of elasticity).Measure the DMS6100 that machine uses SII Nanoentech Co., Ltd. system.In addition, the chuck of fiber distance is set as to 3mm, clamps by arranging 40 filamentous fibre bundles and measured.
Creating conditions of the measurement result of above-mentioned each test and resin kind, tractive multiplying power, stretching ratio etc. is documented in following table 2.
[table 2]
By the embodiment 1~4 that the ratio (tractive multiplying power/stretching ratio) of tractive multiplying power D1 and stretching ratio D2 is set as 1.5~14.0, the ratio of storage elastic modulus (E ' 90/E ' 150) is 3~20, be not baking oven crimpiness, processability, also comparatively excellent on intensity.Wherein, the embodiment 1,4 that the ratio of storage elastic modulus (E ' 90/E ' 150) is 4~10, give especially good results in the baking oven crimpiness.
The ratio (D1/D2) of drawing-off multiplying power D1 and stretching ratio D2 is once be less than 1.5, and the undrawn yarn that too stretches when stretching can cause easily fracture of silk, causes processability deteriorated.On the other hand, the ratio (D1/D2) of tractive multiplying power D1 and stretching ratio D2, once surpass 14.0, can't fully carry out stretch processing (stretching of undrawn yarn), causes hot strength to diminish.
In embodiment 5, the ratio of storage elastic modulus (E ' 90/E ' 150) is 3.6, although baking oven crimpiness and processability are not good but good, even in this scope, but has the characteristic of the sufficient scope of application.In addition, the tractive multiplying power D1 of embodiment 5 is 1.5 with the ratio (D1/D2) of stretching ratio D2, though the ratio of this tractive multiplying power D1 and stretching ratio D2 at 1.5 o'clock, processability also belongs to good scope, but has the characteristic of the scope of application.
In embodiment 6, the ratio of storage elastic modulus (E ' 90/E ' 150) is 18.5, although baking oven crimpiness transitivity (hot strength) is not good but good, even in this scope, but has the characteristic of the sufficient scope of application.In addition, the drawing-off multiplying power D1 of embodiment 6 is 12 with the ratio (D1/D2) of stretching ratio D2, though the ratio of this tractive multiplying power D1 and stretching ratio D2 at 12 o'clock, hot strength (physical property) also belongs to good scope, but has the characteristic of the scope of application.
With respect to this, in the ratio of storage elastic modulus (E ' 90/E ' 150) is less than 3 comparative example 1, its baking oven crimpiness is poor, and surpasses 20 comparative example 2 at the ratio of storage elastic modulus (E ' 90/E ' 150), just the baking oven crimpiness is not inadequate, and intensity is also bad.
The measurement result of the dynamic viscoelastic of embodiment 1 is shown in Fig. 2, and the measurement result of the dynamic viscoelastic of comparative example 1 is shown in Fig. 3.By Fig. 3, can be learnt, even the fiber for artificial hair of comparative example 1 can melting under the high temperature of 240 ℃ yet, keeping storage elastic modulus E ', heat resistance is very high.But, therefore because heat resistance is too high, not only in forming temperature zone (90~150 ℃), also can melting in postforming temperature province (180~240 ℃), make storage elastic modulus E ', loss elastic modulus E " variation less.With respect to this, no matter the rate of change of the fiber for artificial hair of embodiment 1 in forming temperature zone or postforming temperature province is all larger, formability is very high.
Fig. 2,3 symbol M 1 are in the curve of the storage elastic modulus E ' with respect to temperature, mean that storage elastic modulus E ' is for tangent line certain, the zone (vitreousness zone) that is vitreousness by crystalline state, with the symbol M 2 of figure, be illustrated in temperature higher than the high temperature side in vitreousness zone, the tangent line that is the highest transition region by rate of change.As for the curve of this storage elastic modulus E ', at the tangent line M1 by the vitreousness zone and the tangent line M2 by transition region, on crossing intersection point P, the crystalline state disintegration, start melting.From above-mentioned Fig. 2, the temperature coordinate of the intersection point P of the fiber for artificial hair of embodiment 1, in the scope of 180~240 ℃, can be used commercially available curler (heating-up temperature is below 240 ℃) to be processed.With respect to this, the temperature coordinate of the intersection point P of comparative example 1, surpassing on the position of 240 ℃, is difficult to use commercially available curler to be processed.Utilizability on industry
The not special restriction of the purposes of fiber for artificial hair of the present invention, the hair of can be used for hair net, sending out sheet, pigtail, sending and receiving etc. is decorated or the various hair products such as the hair of doll (doll hair).
Claims (5)
1. a fiber for artificial hair, is characterized in that, in the storage elastic modulus E ' with respect to temperature, the storage elastic modulus E ' 90 in the time of 90 ℃ and the ratio E ' 90/E ' 150 of the storage elastic modulus E ' 150 in the time of 150 ℃ are 3~20.
2. fiber for artificial hair according to claim 1, is characterized in that, the curve of the described E ' of the storage elastic modulus with respect to temperature has:
Above-mentioned storage elastic modulus E ' is held certain vitreousness zone; And
Its temperature is maximum transition region higher than above-mentioned vitreousness zone and rate of change,
The temperature coordinate of the intersection point that the tangent line of the described storage elastic modulus E ' curve by described vitreousness zone and the tangent line of described storage elastic modulus E ' curve by described transition region are crossing is positioned at 180~240 ℃.
3. fiber for artificial hair according to claim 1 and 2, is characterized in that, it is by take the resin combination manufacturing that the thermoplastic resin of any one or both in mylar and polyamide is principal component.
4. fiber for artificial hair according to claim 3, its for from the nozzle bore melting sprays described resin combination and manufactures undrawn yarn, the fiber for artificial hair that described undrawn yarn carried out to manufacturing after stretch processing, there is following characteristics,
Be ejected into from melting that to manufacture the ratio D1/D2 of the multiplying power D1 be elongated and the multiplying power D2 that carries out being stretched during stretch processing during undrawn yarn be 1.5~14.0.
5. a hair product, is characterized in that, its right to use requires the described fiber for artificial hair of any one in 1 to 4.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP2011-107896 | 2011-05-13 | ||
JP2011107896 | 2011-05-13 | ||
PCT/JP2012/062133 WO2012157561A1 (en) | 2011-05-13 | 2012-05-11 | Fiber for artificial hair, and hairpiece product |
Publications (1)
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CN103501647A true CN103501647A (en) | 2014-01-08 |
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Family Applications (1)
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CN201280021528.6A Pending CN103501647A (en) | 2011-05-13 | 2012-05-11 | Fiber for artificial hair, and hairpiece product |
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US (1) | US20140109924A1 (en) |
JP (1) | JP5914469B2 (en) |
KR (1) | KR101907049B1 (en) |
CN (1) | CN103501647A (en) |
AP (1) | AP2013007287A0 (en) |
SG (1) | SG194688A1 (en) |
WO (1) | WO2012157561A1 (en) |
ZA (1) | ZA201308463B (en) |
Cited By (1)
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CN107148227A (en) * | 2014-12-09 | 2017-09-08 | 电化株式会社 | Resistance to dripping excellent polyamide-based fiber for artificial hair during burning |
Families Citing this family (3)
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CN107404959B (en) | 2015-03-30 | 2019-06-04 | 株式会社钟化 | Artificial hair acrylic fibers, its manufacturing method and the head decoration product containing it |
CN107708461B (en) | 2015-06-26 | 2019-05-28 | 株式会社钟化 | Artificial hair acrylic fibers, its manufacturing method and the head decoration product comprising it |
JP6682686B1 (en) * | 2019-08-02 | 2020-04-15 | 株式会社アデランス | Method for producing artificial hair for wig and wig |
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Also Published As
Publication number | Publication date |
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KR20140022410A (en) | 2014-02-24 |
JPWO2012157561A1 (en) | 2014-07-31 |
US20140109924A1 (en) | 2014-04-24 |
WO2012157561A1 (en) | 2012-11-22 |
KR101907049B1 (en) | 2018-10-11 |
ZA201308463B (en) | 2015-01-28 |
JP5914469B2 (en) | 2016-05-11 |
AP2013007287A0 (en) | 2013-12-31 |
SG194688A1 (en) | 2013-12-30 |
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