JPS5976906A - Artificial hair material - Google Patents
Artificial hair materialInfo
- Publication number
- JPS5976906A JPS5976906A JP18444782A JP18444782A JPS5976906A JP S5976906 A JPS5976906 A JP S5976906A JP 18444782 A JP18444782 A JP 18444782A JP 18444782 A JP18444782 A JP 18444782A JP S5976906 A JPS5976906 A JP S5976906A
- Authority
- JP
- Japan
- Prior art keywords
- artificial hair
- substrate
- acrylonitrile
- fibers
- coating
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims description 31
- 239000000835 fiber Substances 0.000 claims description 32
- 239000011248 coating agent Substances 0.000 claims description 18
- 238000000576 coating method Methods 0.000 claims description 18
- 239000000758 substrate Substances 0.000 claims description 16
- 229920001577 copolymer Polymers 0.000 claims description 13
- 229920001568 phenolic resin Polymers 0.000 claims description 13
- 229920002647 polyamide Polymers 0.000 claims description 13
- 239000005011 phenolic resin Substances 0.000 claims description 12
- 239000004952 Polyamide Substances 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 9
- 239000002932 luster Substances 0.000 claims description 9
- 229920002292 Nylon 6 Polymers 0.000 claims description 6
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 claims description 4
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 claims description 3
- 229920000299 Nylon 12 Polymers 0.000 claims description 3
- 229920002302 Nylon 6,6 Polymers 0.000 claims description 3
- 229920006026 co-polymeric resin Polymers 0.000 claims description 3
- 239000011342 resin composition Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 7
- 229920002994 synthetic fiber Polymers 0.000 description 7
- 239000012209 synthetic fiber Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000975 dye Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 230000003712 anti-aging effect Effects 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 230000003779 hair growth Effects 0.000 description 2
- 238000009998 heat setting Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 101000650772 Boana raniceps Raniseptin-8 Proteins 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 229920002821 Modacrylic Polymers 0.000 description 1
- 235000008708 Morus alba Nutrition 0.000 description 1
- 240000000249 Morus alba Species 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000013040 bath agent Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000001054 cortical effect Effects 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- 239000002314 hair substitute Substances 0.000 description 1
- 230000003699 hair surface Effects 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001343 mnemonic effect Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- -1 polyhexamethylene phthalate Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000002166 wet spinning Methods 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は、人工毛髪材料の改良技術に係シ、特に機械的
性質と光沢とを改善□することにより、金属光沢を抑え
て、天然毛髪に近い光沢を具えた人工毛髪に係るもので
ある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a technology for improving artificial hair materials, and in particular, by improving mechanical properties and gloss, it is possible to suppress metallic luster and create artificial hair with a luster close to that of natural hair. It is related to hair.
従来から、ライラグ(かつら)、植毛用毛髪などに合成
樹脂からなる繊維か使用されてきたが、これシ、の合成
繊維はポリ塩化ビニール、塩化ビニール−アクリロニト
リル共1合体などであり、その表面れ平滑で金属光沢を
呈し、着用時の違和感が否めなかった。またこの合成繊
維は耐熱性が低く熱セットが容易であるものの形態保持
性が不充分であり、しかも耐溶剤性や機械的強度は満足
できないものである。Traditionally, fibers made of synthetic resin have been used for wigs, hair transplants, etc., but these synthetic fibers are made of polyvinyl chloride, a combination of vinyl chloride and acrylonitrile, etc. It was smooth and had a metallic luster, and I couldn't help but feel uncomfortable when wearing it. Furthermore, although this synthetic fiber has low heat resistance and is easily heat-set, its shape retention is insufficient, and furthermore, its solvent resistance and mechanical strength are unsatisfactory.
本発明は、新しい形状構造と新しい素材とからなる人工
毛髪であって、従来技術の問題点を根本的に改良するも
のである。The present invention is an artificial hair made of a new shape and structure and a new material, which fundamentally improves the problems of the prior art.
まず、本発明の人工毛髪材料は基質と被覆質とからなる
二重構造であって之そ−の断面において芯と鞘とを有す
る構成とすると、とにより、基質部分に機械的強度、耐
熱性を負担させ、被覆質部分において光沢、耐摩耗性、
耐溶剤性を分担させることができる。First, the artificial hair material of the present invention has a double structure consisting of a matrix and a covering material, and has a core and a sheath in cross section. The coating material has gloss, abrasion resistance,
Solvent resistance can be shared.
また、二重構造をもつ人工毛髪材料は表面に微細な凹凸
を形成させることができ、天然毛髪の備えているスケー
ルと類似した効果を呈し、単に光沢のみならず櫛などに
よる引(荊えや、高い摩擦係数に伴う抱合性をもたらす
知見も、ある。In addition, artificial hair materials with a double structure can form fine irregularities on the surface, and exhibit an effect similar to the scale of natural hair. , there are also findings that lead to conjugation with high friction coefficients.
更に、天然毛髪と比較して、人工毛髪は表面を硬質とす
ることが可能であシ、熱セットや薬品によるセットも天
然毛髪よりも優れたものとなし得る。Furthermore, compared to natural hair, artificial hair can have a harder surface and can be set better with heat or chemicals than natural hair.
本発明は、このような改良を目的として鋭意研究した結
果、得られた二重構造をもつ人工毛髪材料である。The present invention is an artificial hair material with a double structure obtained as a result of intensive research aimed at such improvements.
本発明は、芯と鞘とからなる二重構造の人工毛髪材料で
あり、芯はナイロン6、ナイロン66又はナイロン12
等よシなるlO〜50デニールのポリアミド系繊維から
なる基質であシ、鞘はアクリロニトリル−ブタジェン共
重合体と核共重合体に相溶性のフェノール系樹脂とから
なる熱硬化性の組成物であり(該共重合体と該フェノー
ル系樹脂との成分比は重量比において0.4 : 1〜
4:1の範囲であることが望ましい)、該基質の周囲に
被覆されでいてその厚さが0.5〜15μmであること
を%徴とする人工毛髪材料である。The present invention is a double-structured artificial hair material consisting of a core and a sheath, and the core is made of nylon 6, nylon 66 or nylon 12.
The substrate is made of polyamide fibers of 10 to 50 deniers, and the sheath is a thermosetting composition made of an acrylonitrile-butadiene copolymer and a phenolic resin compatible with the core copolymer. (The component ratio of the copolymer and the phenolic resin is 0.4:1 to 1 by weight)
(preferably in the range of 4:1), the artificial hair material is coated around the substrate and has a thickness of 0.5 to 15 μm.
本発明を説明する。The present invention will be explained.
芯と鞘とからなる二重構造の複合繊維hz z種の重合
体又ト重合体溶液を二重紡糸ノズルから紡出させながら
製造する方法と、あらかじめ単一繊維を通常の紡糸(延
伸)技術で得た後にこの単一繊維の周囲に他の重合体を
付着せしめる方法とがある。本発明の人工毛髪材料は前
者でも可能であるが、後者の表面処理法が適している。A method for producing double-structured composite fibers consisting of a core and a sheath by spinning a hzz type of polymer or t-polymer solution from a double spinning nozzle, and a method for producing a single fiber in advance using a conventional spinning (drawing) technique. There is a method in which other polymers are attached around this single fiber after it has been obtained. Although the artificial hair material of the present invention can be treated with the former method, the latter surface treatment method is suitable.
芯鞘構造繊維を溶融成形した場合に認められるような平
滑表面を避け、毛髪表面の有するスケールに近似した表
面凹凸の形成を狙うため、本発明では繊維表面に所゛定
厚−さの樹脂濃厚溶液を塗設するものである。In order to avoid the smooth surface that is observed when core-sheath structure fibers are melt-molded, and aim to form surface irregularities similar to the scales on the hair surface, in the present invention, the fiber surface is coated with a resin-rich resin of a certain thickness. A solution is applied.
本発明の人工毛髪の芯部分は天然毛髪の基質に相当し、
また鞘部分の被S質は天然毛髪の表面のスケールを含む
皮質層に相当するものである。The core portion of the artificial hair of the present invention corresponds to the matrix of natural hair,
The S-substance of the sheath portion corresponds to the cortical layer containing scales on the surface of natural hair.
従って、本発明の基質となる材料は天然毛髪成潅維を検
討したところポリへキサメチレンチンフタレートやポリ
ブチン/テレフタレートのyIJきポリエステルや、ナ
イロン6、ナイロン12、ナイロン66等のポリアミド
が、天然毛髪と同程度の繊維径(直径30〜60μm)
のとき同程度の柔軟性(曲げ硬さ)、ヤング率、剛性率
等を呈することを見い出し、また被覆材(鞘ンとの接着
性、染色性、加熱加工性(熱セット性)等を検討したと
ころ、ナイロン6を含むポリアミド系合成繊維が基質と
して好ましいことを知見した。Therefore, the substrate material of the present invention was examined for natural hair growth fibers, and it was found that polyesters such as polyhexamethylene phthalate, polybutyne/terephthalate, and polyamides such as nylon 6, nylon 12, and nylon 66 were used for natural hair growth fibers. Fiber diameter similar to (30 to 60 μm in diameter)
It was discovered that the same degree of flexibility (bending hardness), Young's modulus, rigidity modulus, etc. was exhibited when As a result, it was found that polyamide synthetic fiber containing nylon 6 is preferable as a substrate.
本発明では、ポリアミド系合成繊維として単一ポリマー
のみでなく、他の重合体、可塑剤。In the present invention, polyamide-based synthetic fibers include not only a single polymer but also other polymers and plasticizers.
添加剤等を含有するポリマーブレンドや1合体組成物が
適用できる。勿論染料や顔料を含有する所餌原着繊維が
好ましく、ポリアミド系合成繊維は溶融紡糸法で得たも
のでよい(湿式法で紡糸することもできる)。繊維径は
曲は硬さを考慮して10〜50デニ一ル8度の範囲にお
いて選択するとよい。Polymer blends and monomer compositions containing additives and the like can be applied. Of course, spun-dyed fibers containing dyes or pigments are preferred, and the polyamide synthetic fibers may be those obtained by melt spinning (wet spinning can also be used). The fiber diameter is preferably selected within the range of 10 to 50 deniers and 8 degrees, taking into account the hardness of the bend.
本発明の人工毛髪材料の被覆γ↓の拐料は、アクリロニ
トリル−ブタジェン共重合体とこの共重合体と相溶性の
あるフェノール系樹脂との組成物である。被檄質となる
組成物材料は、重量比において、共重合体対フェノール
系槌脂が0.4対1乃至4:1の範囲である。The coating material γ↓ of the artificial hair material of the present invention is a composition of an acrylonitrile-butadiene copolymer and a phenolic resin that is compatible with this copolymer. The weight ratio of the composition material used as the material to be machined is in the range of 0.4:1 to 4:1 between copolymer and phenolic hammer fat.
ここに、アクリルニトリル−ブタジェン共重合体として
はアクリロニトリル含量が約28〜421M%のものが
好ましい。アクリロニトリル含量が28亘量チ未満であ
ると組成物として洗rT4I(汚れ除去)、熱セット、
溶剤処理などに対する耐久性が乏しい欠点を゛もつ・。Here, the acrylonitrile-butadiene copolymer preferably has an acrylonitrile content of about 28 to 421 M%. When the acrylonitrile content is less than 28%, the composition can be used for washing rT4I (stain removal), heat setting,
It has the disadvantage of poor durability against solvent treatments, etc.
壕だアクリロニトリル含量が42%を超える。とき、ポ
リアミド系繊維基質に被覆する際の作業性が低くなる。The acrylonitrile content in the trench exceeds 42%. In this case, the workability when coating a polyamide fiber substrate becomes low.
この理由は過大の゛アクリロニトリルを含有する場合は
溶剤可溶性が低くなるからである。The reason for this is that when an excessive amount of acrylonitrile is contained, the solvent solubility becomes low.
また本発明の被憶部となるアクリルニトリル−ブタジェ
ン共重合体には、スチレン、アクリル酸及びメタクリル
酸の如き曲のコモノマーから誘導される単位を含んでも
よい。The acrylonitrile-butadiene copolymer serving as the storage part of the present invention may also contain units derived from common comonomers such as styrene, acrylic acid, and methacrylic acid.
組成物の他の成分となるフェノール系樹脂は、1櫓のフ
ェノールと少なくとも1イ重のアルデヒドから得られる
樹脂及びこれらの変性物であって、前述のアクリルニト
リル−ブタジェン共重合体と相溶性を有するものである
。The phenolic resin, which is another component of the composition, is a resin obtained from one part of phenol and at least one part of aldehyde, or a modified product thereof, and is compatible with the above-mentioned acrylonitrile-butadiene copolymer. It is something that you have.
アクリロニトリル含−礒が比較的高い共重合体の場合は
、通常のフェノール−フォルムアルデヒド初期縮合物も
使用され得るが、一般には油溶性のフェノール系樹脂が
好ましく、その例としてはロジンの如き天然樹脂又Lカ
シューナツトシェルオイルの如き天然油脂で変性された
フェノール系樹脂及び第3級ブチル、第3級アミル、フ
ェニル又はシクロヘキシルの如’ak換基ヲ有スる置換
フェノールとフォルムアルデヒドとの初期縮合物がある
。市販のrDurey 12687J及びrDurey
11098J (Durey PlaMtics 8
Chem−1aal Inc、)、 rc、g、 R
55ln 12316j 及びrG、E。In the case of a copolymer with a relatively high acrylonitrile content, ordinary phenol-formaldehyde initial condensates may also be used, but oil-soluble phenolic resins are generally preferred; examples include natural resins such as rosin. Also, initial condensation of formaldehyde with phenolic resins modified with natural fats and oils such as L-cashew nut shell oil and substituted phenols with ak substituents such as tertiary butyl, tertiary amyl, phenyl or cyclohexyl. There are things. Commercially available rDurey 12687J and rDurey
11098J (Durey PlaMtics 8
Chem-1aal Inc, ), rc, g, R
55ln 12316j and rG,E.
Re5in 12393J (General El
ectric Co、)。Re5in 12393J (General El
etric Co.).
rsynco 721J (Snycl@r Chem
ical Co、)、l−8P−12J及びrsp−8
014J (Shenectacly Re5ins
8 Varni−sh Co、)、rCKRA 197
7J及びrBKR262oJ (Hake−目te C
o、)は本発明の目的のために好適に使用されうる油溶
性フェノール樹脂である。rsynco 721J (Snycl@r Chem
ical Co.), l-8P-12J and rsp-8
014J (Shenectically Re5ins
8 Varni-sh Co, ), rCKRA 197
7J and rBKR262oJ (Hake-eye te C
o,) are oil-soluble phenolic resins that can be suitably used for the purposes of the present invention.
被覆部は、ポリアミド繊維の表面に塗設するものである
から、ポリアミド系繊維基質はその狭面が平滑で強い光
沢を有するものであってもよい。被核材組成物は、被覆
強度、柔軟性、可撓性、被覆材自体の強度等から選択さ
れるとともに、耐桑品性、耐候性(耐光性)からも選択
されたものである。Since the coating portion is applied to the surface of the polyamide fiber, the polyamide fiber substrate may have a smooth narrow surface and a strong luster. The nucleated material composition is selected based on coating strength, softness, flexibility, strength of the coating material itself, etc., and is also selected based on mulberry resistance and weather resistance (light resistance).
本発明の人工毛髪材料の被覆部となる樹脂組成物は、既
述した通り、アク゛リローニトリルーブタジエン共1合
体:フェノール系樹脂(重量比)が0.4 : 1〜4
:1の範囲、好ましくは0.6:1〜3:1である。As mentioned above, the resin composition that becomes the covering part of the artificial hair material of the present invention has a mixture of acrylonitrile-butadiene and phenolic resin (weight ratio) of 0.4:1 to 4.
:1, preferably 0.6:1 to 3:1.
被覆中におけるフェノール糸樹脂成分の倉が過少である
場合は、被憶の強度、耐薬品性及び基質への接着性が充
分でなく、一方過大である場合には、被穣の柔軟性及び
可撓性に劣り人工毛髪は繰返し伸長、屈曲又は摩擦によ
り、基質の繊維と解離し易くなる。If the content of the phenolic thread resin component in the coating is too small, the strength, chemical resistance, and adhesion to the substrate will be insufficient, while if it is too large, the flexibility and flexibility of the coating will be insufficient. Due to its poor flexibility, artificial hair tends to dissociate from the matrix fibers due to repeated stretching, bending, or friction.
上記のアクリロニトリル−ブタジェン共重合体とフェノ
ール系樹脂との硬化した樹脂は更に、ヘキザメチレンチ
トラミンの如きフェノール系4f411)r用硬化剤及
び増粘剤、老化防止剤及びその他の恋加物を含有するこ
とができる。The cured resin of the acrylonitrile-butadiene copolymer and phenolic resin may further contain phenolic 4F411) hardeners and thickeners, anti-aging agents and other additives such as hexamethylene lentithramine. It can contain.
被櫨質の繊維基質の上に設ける塗膜厚さは、毛髪代用品
としての機能を発現する必要から制約される。被覆質の
厚さは下限が0,5μmであり、これは被覆質材料が所
定の外観、金属光沢の抑制、耐疲労性(折曲け、着用等
による被覆質の損傷、クラックの発生)、耐洗濯性(洗
浄等)。The thickness of the coating applied to the fibrous oak substrate is limited by the need to function as a hair substitute. The lower limit of the thickness of the coating material is 0.5 μm, which means that the coating material has a predetermined appearance, suppression of metallic luster, fatigue resistance (damage to the coating material due to bending, wearing, etc., occurrence of cracks), Washing resistance (washing, etc.).
耐摩耗性等から決まる。また塗膜の厚さの上限は基質の
太さにも依存するが、15μmを超えると実用性が殆ど
ない。Determined by wear resistance etc. Further, the upper limit of the thickness of the coating film depends on the thickness of the substrate, but if it exceeds 15 μm, it is hardly practical.
アクリロニトリル−ブタジェン共重合体とフェノール系
樹脂との組成物は、揮発性溶剤に溶解されて、ペースト
を作る。耕成物に好ましい浴剤としてはメチルエチルケ
トン、メチルイソブチルケトン尋のケトン;二塩化エタ
ンの如き基床化炭化水素;酢酸エチルの如きエステル二
塩化エタンの如きニトロ炭化水床;及びこれらの混合物
、並びにこれらとトルエンの如き稀釈剤との混合物であ
る。The composition of acrylonitrile-butadiene copolymer and phenolic resin is dissolved in a volatile solvent to form a paste. Preferred bath agents for cultivated crops include methyl ethyl ketone, methyl isobutyl ketone and other ketones; base hydrocarbons such as ethane dichloride; esters such as ethyl acetate; nitrohydrocarbon beds such as ethane dichloride; and mixtures thereof. and a diluent such as toluene.
そのペースト中には増粘剤、老化防止剤及びその他の添
加剤並びにフェノール糸樹脂用の硬化剤を適宜配合する
ことができる。A thickener, anti-aging agent, other additives, and a curing agent for the phenolic thread resin can be appropriately blended into the paste.
ペーストは浸漬、吹きつけ及び其他の手段で基質繊維に
応用さ些る。必要ならば被覆材が塗布された繊維をスリ
ットに通過させることKよりペーストのピックアップを
調節て16゜次いで繊維を例えは80℃’−1−20℃
の温度で予備乾燥してから、例えは12.0〜210℃
の温度で加熱処理すると、前記のアクリロニトリル−ブ
タジェン共重合体とフェノール系樹脂とは相互に反応し
架橋構造を有する硬化した樹脂となり、繊維基質表面は
安定した被覆質樹脂層により覆われ本発明の人工毛髪を
得ることができる。The paste can be applied to the substrate fibers by dipping, spraying or other means. If necessary, pass the coated fiber through the slit.Adjust the pick-up of the paste from K to 16° and then pass the fiber through the slit, for example 80°C'-1-20°C.
For example, after pre-drying at a temperature of 12.0 to 210℃
When heat-treated at a temperature of You can get artificial hair.
仁の毛髪制料は染料にて目的とする色111AJ K染
色することができるし、又顔料をあらかじめ被租してお
りは後で染色をする必要鉱ない。勿論既述した通り繊維
基質にあらかじめ潅色しておくこともでき、基質と被憶
質とが僅かに色調を異にすることによって、深みのある
色や光沢を創シ出すことが可能となる。Ren's hair dye can be dyed with dye to the desired color, and since it is pre-applied with pigment, there is no need to dye it afterwards. Of course, as mentioned above, the fiber matrix can be colored in advance, and by creating a slight difference in tone between the matrix and the mnemonic material, it is possible to create deep colors and luster. .
以上述べた通り、本発明の人工毛髪材料L1まずポリア
ミド系繊維を製造し5、次いでこの繊維を基質として表
面に樹脂組成物を塗設することによって得ることができ
る。As described above, the artificial hair material L1 of the present invention can be obtained by first producing polyamide fibers 5 and then applying a resin composition to the surface using the fibers as a substrate.
本発明の人工毛髪材料は、基質がポリアミド系合成繊維
であることから、従来のモダクリル繊維やポリ塩化ビニ
ル繊維と比較して耐熱性が高く、シかも熱セット性が良
好である。Since the substrate of the artificial hair material of the present invention is a polyamide-based synthetic fiber, it has higher heat resistance and better heat setting properties than conventional modacrylic fibers or polyvinyl chloride fibers.
更に、強度、破断伸度、耐摩耗性が優れ9合成繊維とし
て柔軟性、風合が好ましく、染色が容易である。また毛
髪程度の繊度をもつモノフィラメントを製造し易い。Furthermore, it has excellent strength, elongation at break, and abrasion resistance, and as a synthetic fiber, it has favorable flexibility and texture, and is easy to dye. Furthermore, it is easy to produce monofilaments with a fineness comparable to that of hair.
このような基p繊維の利点を損うことなく、ポリアミド
系繊維のもつ光沢がギラギラする性質を抑制し、ワキシ
イ感を回避する被a質を備えている。繊維の表面に塗布
した被覆層社平滑ではなく微細な凹凸を形成するため天
然毛髪と類似したスケールの効果も発現している。また
被覆質は硬度を与えることができ、耐薬品性を改善でき
ている。Without impairing the advantages of such basic p-fibers, it has an a-quality coating that suppresses the glittering properties of polyamide fibers and avoids a waxy feel. The coating layer applied to the surface of the fibers is not smooth but has fine irregularities, so it also produces an effect on a scale similar to that of natural hair. Additionally, the coating material can provide hardness and improve chemical resistance.
このように本発明の人工毛髪材料は優れたものであって
、実用性を備えたものである。As described above, the artificial hair material of the present invention is excellent and has practicality.
実施例
カーボンブラック3.5重ill及び酸化チタン0.5
重電−チ含有する固有粘度1.02のナイロン6ペレッ
トを常法で溶融紡糸’l、、Jtちに3.8倍冷m 伸
し、38デニールモノフイ、ラメントを得た。この伶維
は光沢のある黒色を呈していた。Example carbon black 3.5 ill and titanium oxide 0.5
Nylon 6 pellets with an intrinsic viscosity of 1.02 and containing a heavy electric chain were melt-spun by a conventional method and then stretched 3.8 times cold to obtain a 38-denier monofilament. This fiber had a glossy black color.
破瞳樹脂としてアクリロニトリル含有量が35 :1i
−4l1%のアクリルニトリル−ブタジェン共重合体を
使用し、また油溶性のフェノール樹脂として市販のrG
、E、 Re@in t2393J を使用した。Acrylonitrile content is 35:1i as pupil-break resin
-4l1% acrylonitrile-butadiene copolymer was used, and rG, which is commercially available as an oil-soluble phenolic resin, was used.
, E, Re@in t2393J was used.
両名の混合比をl:1とし、メチルエチルケトンに溶解
してペーストを作った。A paste was prepared by dissolving the two in methyl ethyl ketone at a mixing ratio of 1:1.
次にこのペーストに前記ナイロン6繊維を浸漬し、櫛状
のスリットに導びいて被覆樹脂の厚さを約8μnrに調
節し、真空乾燥機(65℃、5〜6 mnHg )によ
り予備乾悼(3時間)シ、更に180℃において40分
間加熱処理した。Next, the nylon 6 fibers were immersed in this paste, guided through a comb-shaped slit to adjust the thickness of the coating resin to about 8 μnr, and pre-dried in a vacuum dryer (65°C, 5-6 mnHg). 3 hours) and further heat-treated at 180° C. for 40 minutes.
得られた繊維は落着いた光沢があり、金属様の光沢が消
え、天然の毛髪と酷似していた。The obtained fibers had a subdued luster, the metallic luster had disappeared, and they closely resembled natural hair.
Claims (3)
=質とからなる人工毛髪材料であって、該基質はポリア
ミド系繊維からなシ、該被覆質はアクリロニトリル−ブ
タジェン共重合体と該共重合体に相溶性の7エノール系
at脂とからなる硬化性の組成物でありかつ該被覆質の
厚サバ0.5〜15ミクロン(μm)であることを特徴
とする人工毛髪材料。(1) A fibrous substrate and a coating that covers the surface of the substrate.
An artificial hair material consisting of an acrylonitrile-butadiene copolymer and a 7-enol AT fat compatible with the copolymer, wherein the substrate is not a polyamide fiber; An artificial hair material characterized in that it is a synthetic hair composition and the thickness of the coating is 0.5 to 15 microns (μm).
ェノール系樹脂との成分比が重1比において0.4 :
1〜4:1の範囲である被覆質からなる特許請求の範
囲第1項記載の人工毛髪材料。(2) The component ratio of acrylonitrile-butadiene copolymer and phenolic resin is 0.4 in weight ratio:
2. An artificial hair material according to claim 1, comprising a covering material having a ratio of 1 to 4:1.
からなる10〜50デニールのポリアミド繊維の表面が
0.5〜15μmの厚さに硬化性樹脂組成つで被覆され
て、基質と被&質とを備えた落ちついた光沢と耐久性を
有する特許請求の範囲第1項又は第2項記載の人工毛髪
材料。(3) Nylon 6, nylon 66 or nylon 12
A patent claim in which the surface of a polyamide fiber of 10 to 50 denier is coated with a curable resin composition to a thickness of 0.5 to 15 μm, and has a subdued luster and durability with a substrate and texture. The artificial hair material according to item 1 or 2.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18444782A JPS5976906A (en) | 1982-10-22 | 1982-10-22 | Artificial hair material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18444782A JPS5976906A (en) | 1982-10-22 | 1982-10-22 | Artificial hair material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5976906A true JPS5976906A (en) | 1984-05-02 |
Family
ID=16153302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18444782A Pending JPS5976906A (en) | 1982-10-22 | 1982-10-22 | Artificial hair material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5976906A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1696072A1 (en) * | 2005-02-24 | 2006-08-30 | Easy Hair Group Holding Limited | Artificial hair or doll's hair |
JP2015096659A (en) * | 2013-11-15 | 2015-05-21 | 株式会社アートネイチャー | Wig base and wig |
-
1982
- 1982-10-22 JP JP18444782A patent/JPS5976906A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1696072A1 (en) * | 2005-02-24 | 2006-08-30 | Easy Hair Group Holding Limited | Artificial hair or doll's hair |
JP2015096659A (en) * | 2013-11-15 | 2015-05-21 | 株式会社アートネイチャー | Wig base and wig |
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