JPH01148806A - Acrylic synthetic fiber for wig - Google Patents
Acrylic synthetic fiber for wigInfo
- Publication number
- JPH01148806A JPH01148806A JP30526187A JP30526187A JPH01148806A JP H01148806 A JPH01148806 A JP H01148806A JP 30526187 A JP30526187 A JP 30526187A JP 30526187 A JP30526187 A JP 30526187A JP H01148806 A JPH01148806 A JP H01148806A
- Authority
- JP
- Japan
- Prior art keywords
- acrylonitrile
- fibers
- hair
- fiber
- halogen
- 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
- 229920002994 synthetic fiber Polymers 0.000 title claims abstract description 19
- 239000012209 synthetic fiber Substances 0.000 title claims abstract description 19
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title claims abstract description 16
- 239000000835 fiber Substances 0.000 claims abstract description 45
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000000178 monomer Substances 0.000 claims abstract description 15
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 11
- 150000002367 halogens Chemical class 0.000 claims abstract description 11
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- 230000003796 beauty Effects 0.000 abstract description 11
- 229920001577 copolymer Polymers 0.000 abstract description 3
- 230000000977 initiatory effect Effects 0.000 abstract 1
- 230000014759 maintenance of location Effects 0.000 description 15
- 238000000034 method Methods 0.000 description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 239000002537 cosmetic Substances 0.000 description 9
- 230000003766 combability Effects 0.000 description 8
- 238000009987 spinning Methods 0.000 description 8
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 229920000058 polyacrylate Polymers 0.000 description 6
- 239000011550 stock solution Substances 0.000 description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000008602 contraction Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000009998 heat setting Methods 0.000 description 3
- 239000002932 luster Substances 0.000 description 3
- 238000007788 roughening Methods 0.000 description 3
- SZHIIIPPJJXYRY-UHFFFAOYSA-M sodium;2-methylprop-2-ene-1-sulfonate Chemical compound [Na+].CC(=C)CS([O-])(=O)=O SZHIIIPPJJXYRY-UHFFFAOYSA-M 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 238000002166 wet spinning Methods 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 229920002821 Modacrylic Polymers 0.000 description 2
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 2
- 230000001680 brushing effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 235000000396 iron Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 150000003606 tin compounds Chemical class 0.000 description 2
- 229920006312 vinyl chloride fiber Polymers 0.000 description 2
- SXZSFWHOSHAKMN-UHFFFAOYSA-N 2,3,4,4',5-Pentachlorobiphenyl Chemical compound C1=CC(Cl)=CC=C1C1=CC(Cl)=C(Cl)C(Cl)=C1Cl SXZSFWHOSHAKMN-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- XEEYSDHEOQHCDA-UHFFFAOYSA-N 2-methylprop-2-ene-1-sulfonic acid Chemical compound CC(=C)CS(O)(=O)=O XEEYSDHEOQHCDA-UHFFFAOYSA-N 0.000 description 1
- FKOZPUORKCHONH-UHFFFAOYSA-N 2-methylpropane-1-sulfonic acid Chemical compound CC(C)CS(O)(=O)=O FKOZPUORKCHONH-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical class [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 150000001463 antimony compounds Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- -1 etc. Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- FWFUWXVFYKCSQA-UHFFFAOYSA-M sodium;2-methyl-2-(prop-2-enoylamino)propane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(C)(C)NC(=O)C=C FWFUWXVFYKCSQA-UHFFFAOYSA-M 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野)
本発明は、かつら、ヘアピース、ドールヘア(人形の頭
髪)、人形以外の玩具や装飾品などの毛髪のごとき部分
などに使用される耐熱性に優れた毛髪用アクリル系合成
繊維に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to heat-resistant materials used in hair-like parts of wigs, hairpieces, doll hair, toys and accessories other than dolls, etc. Concerning excellent acrylic synthetic fibers for hair.
C従来の技術・発明が解決しようとする問題点]一般に
毛髪用に使用されている合成繊維として、モダクリル系
繊維、塩化ビニル系繊維、塩化ビニリデン系繊維がある
。C. Prior Art/Problems to be Solved by the Invention] Synthetic fibers commonly used for hair include modacrylic fibers, vinyl chloride fibers, and vinylidene chloride fibers.
これらの繊維は耐熱性が低いためカールなどの熱セット
は低温で容易に行なうことができるものの、使用してい
るうちにカールの形態が損われやすく、再カールを付与
するための熱セットを繰返すにしたがって繊維が痛み、
後セットが困難となる。また、シャワーや風呂あるいは
サウナなどにおける湿熱下や乾熱下での使用、あるいは
湯浴での洗髪やドライヤーなどによる乾燥、ブラッシン
グなどでも簡単にカールの形態がくずれ、毛髪本来の性
能を維持することが困難であるという問題がある。さら
に、カールなどの形態付与においては、耐熱性が低いた
め形態を保持させる温度は高くてもせいぜい100〜1
10℃が限度であり、これ以上の温度では繊維自体が収
縮し、カール付与には細心の注意と特殊な器具が必要で
、一般の美容院で用いられているヘアードライヤーやヘ
アーアイロンの使用が困難である。These fibers have low heat resistance, so although heat setting such as curling can be easily done at low temperatures, the curl form tends to be damaged while being used, so heat setting must be repeated to recurl. Accordingly, the fibers become sore,
It becomes difficult to set up afterwards. In addition, the shape of the curls can easily be lost and the original performance of the hair can be maintained by using it under moist heat or dry heat in a shower, bath, sauna, etc., washing the hair in a hot water bath, drying it with a hair dryer, or brushing it. The problem is that it is difficult. Furthermore, when imparting shapes such as curls, the heat resistance is low, so the temperature at which the shape is maintained is at most 100 to 1
The temperature limit is 10℃; at temperatures higher than this, the fibers themselves will shrink, and creating curls requires special care and special equipment, making it impossible to use hair dryers or curling irons that are commonly used in beauty salons. Have difficulty.
一方、これらの問題を解決すべくナイロン繊維やポリエ
ステル繊維の表面を化学的、機械的に粗面化し、これら
繊維の有する金属光沢を改良して毛髪用合成繊維を製造
する方法が、特開昭81−245301号公報、特開昭
82−156308号公報、特開昭62−156309
号公報などに開示されている。On the other hand, in order to solve these problems, a method for manufacturing synthetic fibers for hair by chemically and mechanically roughening the surfaces of nylon fibers and polyester fibers and improving the metallic luster of these fibers was proposed in Japanese Patent Application Laid-Open No. 81-245301, JP 82-156308, JP 62-156309
It is disclosed in the publication number etc.
しかし、これらの合成繊維は素材自体の結晶性が高いた
めに耐熱性は高くなるものの、剛直で毛髪用繊維として
大切な美容特性に劣ったものであり(たとえばカールの
形態がタイトであり、スタイラビリティ(再カールなど
の付与性)に劣る)、表面の粗面化処理による金属光沢
の改良では天然毛髪の自然光沢には及ばず、また粗面化
のコントロールも難しく櫛通りがわるくなるといった欠
点を有しており、毛髪用繊維として充分な特性を有して
いるとはいえない。However, although these synthetic fibers have high heat resistance due to the high crystallinity of the material themselves, they are rigid and have inferior beauty properties that are important for hair fibers (for example, the curl form is tight, making it difficult to style). The improvement of metallic luster through surface roughening treatment is not as good as the natural luster of natural hair, and it is also difficult to control the roughening, making it difficult to comb. It cannot be said that it has sufficient properties as a hair fiber.
[問題点を解決するための手段]
本発明は前記従来から検討されている毛髪用合成繊維の
問題点を解決し、カール付与に特殊な器具が不要で、通
常の美容熱器具で容品にカールを付与することができ、
乾熱下または湿熱下においてもカールの形態保持性が良
好な毛髪用アクリル系合成繊維を提供するためになされ
たものであり、アクリロニトリル成分50〜70%(重
量%、以下同様)およびアクリロニトリルと共重合可能
なハロゲン含有単量体成分25〜50%を含有し、アク
リロニトリル成分とハロゲン含有単量体成分の合計量が
重合体の90%以上である重合体よりなり、繊維の収縮
開始温度(T0)が140〜200℃である毛髪用アク
リル系合成繊維に関する。[Means for Solving the Problems] The present invention solves the problems of the synthetic fibers for hair that have been considered in the past, and does not require any special equipment for curling, and can be applied to hair using ordinary beauty heating equipment. Can give curls,
This was developed to provide an acrylic synthetic fiber for hair that has good curl shape retention even under dry heat or wet heat, and contains an acrylonitrile component of 50 to 70% (wt%, same hereinafter) and acrylonitrile. It is made of a polymer containing 25 to 50% of a polymerizable halogen-containing monomer component, in which the total amount of the acrylonitrile component and the halogen-containing monomer component is 90% or more of the polymer, and the fiber shrinkage onset temperature (T0 ) is 140 to 200°C.
[実施例]
本発明の毛髪用アクリル系合成繊維とは、かつら、ヘア
ピース、ドールヘア、人形以外の玩具や装飾品などの毛
髪のごとき部分などに使用されるアクリル系合成繊維で
ある。[Example] The acrylic synthetic fiber for hair of the present invention is an acrylic synthetic fiber used for hair-like parts of wigs, hairpieces, doll hair, toys and accessories other than dolls, and the like.
本発明のアクリル系合成繊維はアクリロニトリル成分を
50〜70%、アクリロニトリルと共重合可能なハロゲ
ン含有単量体成分を25〜5026含有している共重合
体からなっている。The acrylic synthetic fiber of the present invention is made of a copolymer containing 50 to 70% acrylonitrile component and 25 to 5026 halogen-containing monomer components copolymerizable with acrylonitrile.
前記アクリロニトリル成分の含有率が50%未満になる
と、耐熱性が不充分となり、形態保持性に問題が生じる
。また美容熱器具によるリスタイル作業が困難などの毛
髪用繊維として必要な特性を充分保持することができな
くなる。−方、70%をこえるとカールの形態保持性は
良好になるが毛髪用繊維として必要な美容特性、とくに
スタイルのアレンジ性や櫛通り性などに問題が生じやす
くなる。なお、アクリロニトリル成分の含有量は50〜
65%のものがさらに好ましく、とくに該含有量が50
〜60%のものが好ましい。When the content of the acrylonitrile component is less than 50%, heat resistance becomes insufficient and problems arise in shape retention. Further, it becomes difficult to perform a restyling operation using a cosmetic heating device, and it becomes impossible to sufficiently maintain the properties necessary for hair fibers. - On the other hand, if it exceeds 70%, the shape retention of curls is good, but problems tend to occur in the cosmetic properties necessary for hair fibers, particularly in the ease of styling and combability. In addition, the content of acrylonitrile component is 50~
It is more preferable that the content is 65%, especially when the content is 50%.
~60% is preferred.
また、前記ハロゲン含有単量体成分が25〜50%のば
あいには、アクリロニトリルとハロゲン含有単量体とを
主成分とする重合体からの毛髪用繊維のたとえばカール
の形態保持性やスタイルのアレンジ性、櫛通り性などの
美容特性や難燃性などが優れたものとなるが、該割合が
25%未満では難燃性が不足しがちになる。なお、難燃
性は、毛髪用繊維が身につけたり装飾品などとして身近
におくものであるから望まれる性能である。一方、該割
合が50%をこえると難燃性は向上するが、カールの付
与および形態保持に必要な耐熱性が充分でなくなる。In addition, when the halogen-containing monomer component is 25 to 50%, hair fibers made from a polymer mainly composed of acrylonitrile and a halogen-containing monomer, for example, can improve curl shape retention and style. It has excellent beauty properties such as arrangeability and combability, and flame retardancy, but if the proportion is less than 25%, the flame retardance tends to be insufficient. Incidentally, flame retardancy is a desired performance since hair fibers are worn on the body or kept close at hand as ornaments. On the other hand, if the ratio exceeds 50%, the flame retardance will improve, but the heat resistance required for curling and shape retention will not be sufficient.
前記ハロゲン含有単量体の具体例としては、塩化ビニル
、塩化ビニリデン、臭化ビニル、臭化ビニリデンなどの
単量体があげられるが、これらに限定されるものではな
い。これらは単独で用いてもよく、2種以上併用しても
よい。Specific examples of the halogen-containing monomer include, but are not limited to, vinyl chloride, vinylidene chloride, vinyl bromide, and vinylidene bromide. These may be used alone or in combination of two or more.
前記アクリロニトリルとハロゲン含有単量体とを主成分
とする重合体は10%以下の範囲でその他の共重合可能
な単量体成分を含有してもよい。このような他の単量体
の具体例としては、たとえばアクリル酸、メタクリル酸
、それらのエステル、アクリルアミド、メタクリルアミ
ド、酢酸ビニル、アリルスルホン酸、メタリルスルホン
酸、スチレンスルホン酸、2−アクリルアミド−2−メ
チルプロパンスルホン酸、これらの塩類などがあげられ
る。The polymer containing acrylonitrile and a halogen-containing monomer as main components may contain other copolymerizable monomer components within a range of 10% or less. Specific examples of such other monomers include acrylic acid, methacrylic acid, esters thereof, acrylamide, methacrylamide, vinyl acetate, allylsulfonic acid, methallylsulfonic acid, styrenesulfonic acid, 2-acrylamide- Examples include 2-methylpropanesulfonic acid and salts thereof.
前記のごとき材質を有する本発明の繊維の耐熱性は、繊
維の収縮開始温度(T0)が140〜200℃、好まし
くは140〜190℃の範囲のものである。なお、参考
としてのこれらの繊維の10%収縮温度(Tl0)は1
55〜210℃の範囲の値である。The heat resistance of the fiber of the present invention having the above-mentioned materials is such that the shrinkage start temperature (T0) of the fiber is in the range of 140 to 200°C, preferably 140 to 190°C. For reference, the 10% contraction temperature (Tl0) of these fibers is 1
The value is in the range of 55-210°C.
本発明のアクリル系合成繊維の収縮開始温度(T0)を
140〜200℃と規定したのは、これらの温度未満の
繊維ではカール付与などのための熱セットは低温で容易
に行なうことができるものの、カールの形態が経時的に
あるいはシャンプーなどで損われやすく、再カールを付
与するための後セットでの温度管理が難しく、かつ繰返
しセットするにしたがって繊維が痛み、短期で後セット
が不可能となるため、このようにならないようにするた
めである。また、シャワーや風呂あるいはサウナなどに
おける湿熱下や乾熱下での使用、あるいは湯浴での洗髪
やドライヤーなどによる乾燥、ブラッシングなどで簡単
にカールの形態がくずれ、毛髪のスタイルを維持するこ
とが困難であるからである。さらに、これらの温度をこ
える繊維では、耐熱性は向上するが剛直性が増し、毛髪
として用いたばあいのスタイルのアレンジ性や櫛通り性
などが劣るからである。The reason why the shrinkage start temperature (T0) of the acrylic synthetic fiber of the present invention is defined as 140 to 200°C is because fibers at temperatures below these temperatures can be easily heat-set for curling at low temperatures. , the shape of the curl is easily damaged over time or by shampooing, etc., it is difficult to control the temperature during post-setting to re-curl, and the fibers become damaged with repeated setting, making post-setting impossible in a short period of time. This is to prevent this from happening. In addition, the shape of the curls can easily be lost and the style of the hair can be maintained by using it under moist or dry heat in a shower, bath, sauna, etc., washing it in a hot water bath, drying it with a hair dryer, or brushing it. This is because it is difficult. Furthermore, fibers that exceed these temperatures have improved heat resistance but increased stiffness, and when used as hair, have poor styling ability and combability.
前記収縮開始温度(T0)および10%収縮温度(Tl
0)とは、繊維に0.81g/デニール(d)の荷重を
かけ、3℃/分の速度で昇温したときに繊維の収縮する
長さを連続的に測定し、繊維が収縮を開始する温度(接
線法)をT。S10%の収縮率を示したときの温度をT
10と定めたものである。The contraction start temperature (T0) and the 10% contraction temperature (Tl
0) means that a load of 0.81 g/denier (d) is applied to the fiber and the length of the shrinkage of the fiber is continuously measured when the temperature is raised at a rate of 3°C/min, and the fiber starts to shrink. The temperature (tangential method) to be T. The temperature when S shows a shrinkage rate of 10% is T
10.
本発明の繊維の断面形状にはとくに限定はなく、円型、
楕円型、馬蹄型や異型断面あるいはこれらを混合したも
のが目的に応じて用いることができる。また20〜70
d1好ましくは40〜55dの繊維が本発明に好適に用
いることができる。There are no particular limitations on the cross-sectional shape of the fibers of the present invention, such as circular,
An elliptical shape, a horseshoe shape, an irregular cross section, or a mixture of these can be used depending on the purpose. Also 20-70
Fibers with d1, preferably 40 to 55 d, can be suitably used in the present invention.
つぎに本発明の繊維を構成するアクリロニトリル系重合
体を製造する方法、該重合体から繊維を製造する方法に
ついて説明する。Next, a method for producing an acrylonitrile polymer constituting the fiber of the present invention and a method for producing fiber from the polymer will be explained.
本発明の繊維を構成する重合体は、前述の単量体を所定
の割合で水性媒体中もしくは有機溶剤中で乳化重合法ま
たは懸濁重合法あるいは溶液重合法のごとき通常の方法
によって重合させることにより製造される。The polymer constituting the fiber of the present invention can be obtained by polymerizing the aforementioned monomers in a predetermined ratio in an aqueous medium or an organic solvent by a conventional method such as an emulsion polymerization method, a suspension polymerization method, or a solution polymerization method. Manufactured by.
このようにしてえられたアクリル系重合体から前記良好
な耐熱性を有し、結果として良好なカールの形態保持性
を有し、スタイルのアレンジ性、櫛通り性などで代表さ
れる美容特性に優れた繊維を製造する方法として、通常
の湿式紡糸法、乾式紡糸法、半乾半湿式紡糸法などがあ
げられ、いずれの方法でも紡糸しうるが、とくに湿式紡
糸法が好ましい。The acrylic polymer obtained in this way has the above-mentioned good heat resistance, and as a result, has good curl shape retention, and has excellent beauty properties such as style arrangement and combability. Examples of methods for producing excellent fibers include conventional wet spinning, dry spinning, semi-dry and semi-wet spinning, and any of these methods may be used, but wet spinning is particularly preferred.
紡糸原液を調製する溶剤としては、通常のアクリロニト
リル系重合体の溶剤であるアセトニトリル、アセトン、
ジメチルホルムアミド、ジメチルアセトアミド、ジメチ
ルスルホキシドなどが用いられる。The solvent for preparing the spinning dope is acetonitrile, acetone, which is a usual solvent for acrylonitrile polymers,
Dimethylformamide, dimethylacetamide, dimethylsulfoxide, etc. are used.
紡糸原液中の重合体濃度は15〜40%であるのが好ま
しい。The polymer concentration in the spinning dope is preferably 15 to 40%.
なお、紡糸原液または溶液重合法の重合系には、必要に
応じて安定剤であるエポキシ化合物、有機錫化合物、有
機還元剤、無機酸、有機酸などや、風合・光沢を改良す
るためのチタン化合物、アルミニウム化合物などの添加
剤、さらには難燃性をさらに高めるためのアンチモン化
合物、スズ化合物、塩素化合物、臭素化合物、リン化合
物などの難燃剤などを含有せしめても何らさしつかえな
い。In addition, the spinning stock solution or the polymerization system of the solution polymerization method may contain stabilizers such as epoxy compounds, organic tin compounds, organic reducing agents, inorganic acids, organic acids, etc., as well as agents to improve texture and gloss. There is no problem in including additives such as titanium compounds and aluminum compounds, and also flame retardants such as antimony compounds, tin compounds, chlorine compounds, bromine compounds, and phosphorus compounds to further improve flame retardancy.
紡糸方法としては紡糸原液をノズルを通じて10〜80
%の溶剤を含有する水溶液中あるいは熱風中に押し出し
て糸条を形成させ、ついで水洗・延伸・乾燥し、そのの
ち必要に応じてさらに延伸を施したのち、熱処理を行な
うという通常の紡糸方法をとればよい。As for the spinning method, the spinning stock solution is passed through a nozzle to
The conventional spinning method is to extrude into an aqueous solution or hot air containing 50% solvent to form a thread, then wash with water, stretch and dry, then further stretch as necessary, and then heat treat. Just take it.
このようにしてえられる本発明の繊維は、耐熱性が優れ
ているにもかかわらずスタイルのアレンジ性にも優れ、
さらに櫛通り性などがよ(美容特性に優れたかつらにす
ることができる。The fiber of the present invention obtained in this way has excellent heat resistance, but also has excellent styling flexibility.
It also has good combability (it can be used to make wigs with excellent beauty properties).
以下、本発明の繊維を実施例に基づきさらに具体的に説
明するが、本発明はこれら実施例に限定されるものでは
ない。EXAMPLES Hereinafter, the fibers of the present invention will be explained in more detail based on Examples, but the present invention is not limited to these Examples.
実施例中のカール保持性の測定は、繊維を直径18關の
パイプに巻付け、オーブン中120℃で40分間熱セツ
トしたサンプルを用いてかつらを作製し、これを150
℃の熱風中と50℃の温水中に30分間放置したときの
カールの伸びを観察して行なった。The curl retention properties in the examples were measured by winding the fibers around a pipe with a diameter of 18 mm and heat setting the sample in an oven at 120°C for 40 minutes to make a wig.
The curl growth was observed after being left in hot air at 50°C and hot water at 50°C for 30 minutes.
実施例1
アクリロニトリル54%、塩化ビニリデン35%、臭化
ビニル9%、メタリルスルホン酸ソーダ2%からなるア
クリル系重合体をジメチルホルムアミドに溶解して30
%の紡糸原液を調製し、60%のジメチルホルムアミド
水溶液中に湿式紡糸し、ついで水洗・延伸・乾燥を行な
い、さらに140℃の熱風中で2.5倍に延伸してから
120℃の水蒸気中で20%の弛緩熱処理を行なった。Example 1 An acrylic polymer consisting of 54% acrylonitrile, 35% vinylidene chloride, 9% vinyl bromide, and 2% sodium methallylsulfonate was dissolved in dimethylformamide to give 30%
% spinning stock solution was prepared, wet-spun in a 60% dimethylformamide aqueous solution, then washed with water, stretched, and dried, further stretched 2.5 times in hot air at 140°C, and then in steam at 120°C. A 20% relaxation heat treatment was performed.
このようにしてえられた50dのアクリル系合成繊維は
収縮開始温度(T0)が175℃、10%収縮温度(T
l0)が186℃であった。The 50 d acrylic synthetic fiber obtained in this way has a shrinkage start temperature (T0) of 175°C and a 10% shrinkage temperature (T
l0) was 186°C.
この繊維のカール保持性を測定したところ、カールの伸
びはほとんどなかった。また、かつらのスタイルのアレ
ンジ性もよく、櫛通り性などの美容特性も良好であった
。When the curl retention of this fiber was measured, there was almost no curl elongation. In addition, the wigs were easy to style and had good beauty properties such as combability.
えられたかつらについてサウナで着用テストを行なった
ところ、カールは伸びることなく形態を保持しており、
40℃の温水で洗髪後、ヘアドライヤーで乾燥しても何
ら支障なく、当初の形態を保持していた。When we tested the resulting wig in a sauna, the curls held their shape without stretching.
After washing the hair with warm water at 40°C, it remained in its original shape without any problems even when dried with a hair dryer.
結果を第1表に示す。The results are shown in Table 1.
実施例2
アクリロニトリル52%、塩化ビニリデン47%、スチ
レンスルホン酸ソーダ1%からなるアクリル系重合体に
、少量の有機錫系化合物を安定剤として加えてアセトン
に溶解させ、28%の紡糸原液を調製した。この原液を
25%のアセトン水溶液中に湿式紡糸し、ついで水洗・
延伸・乾燥を行ない、さらに120℃の熱風中で3.0
倍に延伸してから160℃で弛緩熱処理を行なった。Example 2 A small amount of an organotin compound was added as a stabilizer to an acrylic polymer consisting of 52% acrylonitrile, 47% vinylidene chloride, and 1% sodium styrene sulfonate, and the mixture was dissolved in acetone to prepare a 28% spinning stock solution. did. This stock solution was wet-spun in a 25% acetone aqueous solution, then washed with water.
After stretching and drying, the film was further stretched to 3.0 in hot air at 120°C.
After stretching the film to double its original size, a relaxation heat treatment was performed at 160°C.
このようにしてえられた45dのアクリル系合成繊維は
T が163℃、T10が178℃であった。The 45d acrylic synthetic fiber thus obtained had a T of 163°C and a T10 of 178°C.
この繊維のカール保持性を測定したところ、カールの伸
びはほとんどなかった。またかつらの美容特性も良好で
あった。この繊維を用いてかつらを作製し、カールの形
態を検討したが、140〜150℃の高温でもカールの
付与が可能であり、またカールのリセットも良好であり
、市販のドライヤーでセット、リセットが充分可能であ
った。When the curl retention of this fiber was measured, there was almost no curl elongation. The cosmetic properties of the wig were also good. We made a wig using this fiber and examined the curl form, and found that it was possible to create curls even at high temperatures of 140 to 150 degrees Celsius, and that the curls were reset well, and could be set and reset using a commercially available hair dryer. It was quite possible.
比較例1
アクリロニトリル46%、塩化ビニリデン53%、メタ
リルスルホン酸ソーダ1%からなる共重合体゛を実施例
2と同様にして紡糸・延伸・弛緩熱処理してアクリル系
合成繊維を製造した。Comparative Example 1 A copolymer consisting of 46% acrylonitrile, 53% vinylidene chloride, and 1% sodium methallylsulfonate was spun, drawn, and heat-treated for relaxation in the same manner as in Example 2 to produce an acrylic synthetic fiber.
この繊維のT は137℃、T10は149℃と低く、
実施例1と同様にして評価した美容特性は良好であった
が、カール保持性はわるかった。This fiber has a low T of 137℃ and T10 of 149℃.
The cosmetic properties evaluated in the same manner as in Example 1 were good, but the curl retention was poor.
結果を第1表に示す。The results are shown in Table 1.
比較例2
アクリロニトリル73%、塩化ビニル23%、アクリル
酸メチル3%、メタリルスルホン酸ソーダ196からな
るアクリル系重合体を実施例1と同様に紡糸・延伸・弛
緩水蒸気処理してアクリル系合成繊維をえた。Comparative Example 2 An acrylic polymer consisting of 73% acrylonitrile, 23% vinyl chloride, 3% methyl acrylate, and 196 sodium methallylsulfonate was spun, stretched, and relaxed with steam in the same manner as in Example 1 to produce an acrylic synthetic fiber. I got it.
この繊維のToは186℃、T10は202℃と耐熱性
に優れ、実施例1と同様にして評価したカール保持性も
良好であったが、櫛通り性かわるく、スタイルのアレン
ジ性も不良で、美容特性はよくなかった。結果を第1表
に示す。This fiber had excellent heat resistance with a To of 186°C and a T10 of 202°C, and the curl retention evaluated in the same manner as in Example 1 was also good, but the combability was poor and the style arrangement was poor. , the cosmetic properties were not good. The results are shown in Table 1.
実施例3
アクリロニトリル63%、塩化ビニリデン25%、塩化
ビニル10%、スチレンスルホン酸ソーダ1%、ポリエ
チレングリコールモノメタクリレート1%からなるアク
リル系重合体を実施例1と同様にして紡糸・延伸・弛緩
水蒸気処理してアクリル系合成繊維を製造した。Example 3 An acrylic polymer consisting of 63% acrylonitrile, 25% vinylidene chloride, 10% vinyl chloride, 1% sodium styrene sulfonate, and 1% polyethylene glycol monomethacrylate was spun, stretched, and relaxed with steam in the same manner as in Example 1. The process was carried out to produce acrylic synthetic fibers.
この繊維のT は188℃、”10は199℃と耐熱性
に優れ、カール保持性や美容特性も良好であった。結果
を第1表に示す。The fiber had excellent heat resistance, T of 188°C, and T of 10 of 199°C, as well as good curl retention and cosmetic properties.The results are shown in Table 1.
なお、製造したかつらについて真夏の海で1力月間着用
テストを行なったが、カール保持性は良好であり、シャ
ワー後ドライヤーで乾燥しても、かつらの形態に何ら変
化は認められなかった。The manufactured wig was worn for one month at the sea in midsummer, and the curl retention was good, and no change was observed in the shape of the wig even when it was dried with a hair dryer after a shower.
比較例3〜4
市販のモダクリル繊維および塩化ビニル繊維(それぞれ
比較例3および4)を用いてT。、T10’カール保持
性、美容特性を実施例1と同様にして測定したが、第1
表に示したように、美容特性以外の特性の劣ったもので
あった。Comparative Examples 3-4 T using commercially available modacrylic fibers and vinyl chloride fibers (Comparative Examples 3 and 4, respectively). , T10' curl retention, and beauty properties were measured in the same manner as in Example 1.
As shown in the table, the properties other than cosmetic properties were inferior.
実施例4
アクリロニトリル6996、塩化ビニリデン27%、ア
クリル酸メチル2%、2−アクリルアミド−2−メチル
プロパンスルホン酸ソーダ2%からなるアクリル系重合
体を実施例1と同様にして紡糸・延伸・弛緩水蒸気処理
してアクリル系合成繊維を製造した。Example 4 An acrylic polymer consisting of acrylonitrile 6996, 27% vinylidene chloride, 2% methyl acrylate, and 2% sodium 2-acrylamido-2-methylpropanesulfonate was spun, stretched, and relaxed with steam in the same manner as in Example 1. The process was carried out to produce acrylic synthetic fibers.
この繊維のT。は191”c、Tloは204℃と耐熱
性に優れ、カール保持性も良好であったが、櫛通り性や
スタイルのアレンジ性はやや劣ったものであった。T of this fiber. had excellent heat resistance of 191"c and 204°C for Tlo, and had good curl retention, but the combability and style arrangement were somewhat poor.
〔以下余白]
[発明の効果]
本発明の繊維を用いて、かつら、ヘアピース、ドールヘ
ア、人形以外の玩具や装飾品などの毛髪のごとき部分な
どを製造すると、一般の美容院で用いられている通常の
器具であるヘアードライヤーやヘアーアイロンによって
カールの形態付与が容易で、高温の乾熱または湿熱下に
おいてもカールの形態保持性が良好なものかえられる。[Margins below] [Effects of the Invention] When the fibers of the present invention are used to manufacture hair-like parts of wigs, hairpieces, doll hair, toys other than dolls, ornaments, etc., the fibers of the present invention can be used in general beauty salons. Curls can be easily formed using common tools such as hair dryers and curling irons, and the curls retain their shape well even under high-temperature dry heat or moist heat.
耐熱性が大きすぎると通常の美容熱器具では再カールな
どの後セットが困難となるが、本発明の繊維では通常の
美容熱器具で後セットが可能であるという利点がある。If the heat resistance is too high, it will be difficult to perform post-setting such as re-curling using a normal beauty heating device, but the fiber of the present invention has the advantage that it can be post-setting using a normal cosmetic heating device.
また、かつらの美容特性も良好となる。Moreover, the cosmetic properties of the wig are also improved.
特許出願人 鐘淵化学工業株式会社Patent applicant Kanebuchi Chemical Industry Co., Ltd.
Claims (1)
リロニトリルと共重合可能なハロゲン含有単量体成分2
5〜50重量%を含有し、アクリロニトリル成分とハロ
ゲン含有単量体成分の合計量が重合体の90重量%以上
である重合体よりなり、繊維の収縮開始温度(T_0)
が140〜200℃である毛髪用アクリル系合成繊維。1 Acrylonitrile component 50 to 70% by weight and halogen-containing monomer component copolymerizable with acrylonitrile 2
5 to 50% by weight, and the total amount of the acrylonitrile component and the halogen-containing monomer component is 90% by weight or more of the polymer, and the fiber shrinkage start temperature (T_0)
An acrylic synthetic fiber for hair having a temperature of 140 to 200°C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30526187A JPH01148806A (en) | 1987-12-02 | 1987-12-02 | Acrylic synthetic fiber for wig |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30526187A JPH01148806A (en) | 1987-12-02 | 1987-12-02 | Acrylic synthetic fiber for wig |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01148806A true JPH01148806A (en) | 1989-06-12 |
Family
ID=17942971
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30526187A Pending JPH01148806A (en) | 1987-12-02 | 1987-12-02 | Acrylic synthetic fiber for wig |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01148806A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991015525A1 (en) * | 1990-04-09 | 1991-10-17 | Mitsubishi Rayon Co., Ltd. | Acrylonitrile copolymer and fiber or core-sheath type composite fiber produced therefrom |
US5234766A (en) * | 1990-04-09 | 1993-08-10 | Mitsubishi Rayon Co., Ltd. | Acrylonitrile copolymer, and fiber or core-sheath conjugate fiber prepared therefrom |
WO2002061187A1 (en) * | 2001-01-29 | 2002-08-08 | Kaneka Corporation | Artificial hair and method for production thereof |
JP2002227018A (en) * | 2001-01-29 | 2002-08-14 | Kanegafuchi Chem Ind Co Ltd | Artificial hair |
WO2004013389A1 (en) * | 2002-08-01 | 2004-02-12 | Kaneka Corporation | Acrylic synthetic fiber improved in styleability |
JP2008007891A (en) * | 2006-06-29 | 2008-01-17 | Asahi Kasei Chemicals Corp | Vinylidene chloride-based artificial hair |
WO2016208630A1 (en) * | 2015-06-26 | 2016-12-29 | 株式会社カネカ | Acrylic copolymer, acrylic fiber for artificial hair and method for manufacturing same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS584809A (en) * | 1981-06-29 | 1983-01-12 | Kanegafuchi Chem Ind Co Ltd | Synthetic fiber |
JPS601401A (en) * | 1983-06-17 | 1985-01-07 | Hitachi Koki Co Ltd | Stuffer |
-
1987
- 1987-12-02 JP JP30526187A patent/JPH01148806A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS584809A (en) * | 1981-06-29 | 1983-01-12 | Kanegafuchi Chem Ind Co Ltd | Synthetic fiber |
JPS601401A (en) * | 1983-06-17 | 1985-01-07 | Hitachi Koki Co Ltd | Stuffer |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991015525A1 (en) * | 1990-04-09 | 1991-10-17 | Mitsubishi Rayon Co., Ltd. | Acrylonitrile copolymer and fiber or core-sheath type composite fiber produced therefrom |
US5234766A (en) * | 1990-04-09 | 1993-08-10 | Mitsubishi Rayon Co., Ltd. | Acrylonitrile copolymer, and fiber or core-sheath conjugate fiber prepared therefrom |
US5264531A (en) * | 1990-04-09 | 1993-11-23 | Mitsubishi Rayon Co., Ltd. | Acrylonitrile copolymer, and fiber or core-sheath conjugate fiber prepared therefrom |
WO2002061187A1 (en) * | 2001-01-29 | 2002-08-08 | Kaneka Corporation | Artificial hair and method for production thereof |
JP2002227018A (en) * | 2001-01-29 | 2002-08-14 | Kanegafuchi Chem Ind Co Ltd | Artificial hair |
US6770364B2 (en) | 2001-01-29 | 2004-08-03 | Kaneka Corporation | Artificial hair and method for production thereof |
CN100352978C (en) * | 2001-01-29 | 2007-12-05 | 钟渊化学工业株式会社 | Artificial hair and method for production thereof |
WO2004013389A1 (en) * | 2002-08-01 | 2004-02-12 | Kaneka Corporation | Acrylic synthetic fiber improved in styleability |
US7135225B2 (en) | 2002-08-01 | 2006-11-14 | Kaneka Corporation | Acrylic synthetic fiber improved in styleability |
JP2008007891A (en) * | 2006-06-29 | 2008-01-17 | Asahi Kasei Chemicals Corp | Vinylidene chloride-based artificial hair |
WO2016208630A1 (en) * | 2015-06-26 | 2016-12-29 | 株式会社カネカ | Acrylic copolymer, acrylic fiber for artificial hair and method for manufacturing same |
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