JPS5876252A - Hair implanted product - Google Patents
Hair implanted productInfo
- Publication number
- JPS5876252A JPS5876252A JP17482481A JP17482481A JPS5876252A JP S5876252 A JPS5876252 A JP S5876252A JP 17482481 A JP17482481 A JP 17482481A JP 17482481 A JP17482481 A JP 17482481A JP S5876252 A JPS5876252 A JP S5876252A
- Authority
- JP
- Japan
- Prior art keywords
- flocked
- microspheres
- product
- adhesive layer
- foaming
- 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.)
- Granted
Links
- 210000004209 hair Anatomy 0.000 title claims description 9
- 238000005187 foaming Methods 0.000 claims description 29
- 239000000853 adhesive Substances 0.000 claims description 26
- 230000001070 adhesive effect Effects 0.000 claims description 26
- 239000004005 microsphere Substances 0.000 claims description 24
- 239000000463 material Substances 0.000 claims description 23
- 239000012790 adhesive layer Substances 0.000 claims description 21
- 239000006260 foam Substances 0.000 claims description 21
- 229920000103 Expandable microsphere Polymers 0.000 claims description 15
- 239000000835 fiber Substances 0.000 claims description 15
- 229920001577 copolymer Polymers 0.000 claims description 8
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 229920001169 thermoplastic Polymers 0.000 claims description 7
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 6
- CRSOQBOWXPBRES-UHFFFAOYSA-N neopentane Chemical compound CC(C)(C)C CRSOQBOWXPBRES-UHFFFAOYSA-N 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 5
- 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 claims description 4
- 229920001328 Polyvinylidene chloride Polymers 0.000 claims description 4
- 239000005033 polyvinylidene chloride Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 239000004744 fabric Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 238000000034 method Methods 0.000 description 16
- 239000000839 emulsion Substances 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 230000035699 permeability Effects 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000010985 leather Substances 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 238000002054 transplantation Methods 0.000 description 4
- 229920000459 Nitrile rubber Polymers 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- -1 acrylic ester Chemical class 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-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
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Landscapes
- Laminated Bodies (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、通気性があり、かつボリュームに富み回復弾
性に優れた植毛製品に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a flocked hair product that is breathable, voluminous, and has excellent recovery elasticity.
従来の植毛製品においては、短繊維を基材に接着する接
着層は連続的な薄い塗膜層で形成されているため、通気
性がないのみならず、ボリューム感に乏しく、たとえ、
伸縮性の基材を使用したとしてもその伸縮性を充分発揮
し得ないものであった。そのため、これらの欠点を解消
すべく、例えば発泡塩化ビニルレザー(裏面メリヤス)
を基材として使用したり、あるいは基拐自身ボリューム
感のあるネル、又はダブルニット等を基材として使用し
て来た。In conventional flocked products, the adhesive layer that adheres short fibers to the base material is formed of a continuous thin coating layer, which not only lacks breathability but also lacks volume.
Even if a stretchable base material was used, its stretchability could not be fully demonstrated. Therefore, in order to eliminate these drawbacks, for example, foamed vinyl chloride leather (knitted back side)
has been used as a base material, or flannel, which has a voluminous feel, or double knit, etc., have been used as a base material.
しかし、これらの方法によるものに於いてバー長−短が
あった。例えば、塩ビレザーの場合、ドライクリーニン
グの際に多くの問題点を抱えている。即ち、塩ビに接着
するよい接着剤がないためパイルが取れたり、又、塩ビ
レザーに使用されている可塑剤が抽出され風合が硬くな
ったシする等である。However, in these methods, there were differences in bar length and shortness. For example, PVC leather has many problems during dry cleaning. That is, the pile may come off because there is no good adhesive to adhere to PVC leather, or the plasticizer used in PVC leather may be extracted and the texture may become hard.
又、ボリューム感のあるネル又はダブルニット等を使用
するとしても、風合的に思うような柔軟な植毛品を得る
ことは困難である。殊にボリューム感のあるネル又はダ
ブルニット等は非常に高価なため、最終的には高価な植
毛品となり適切でないO
また、通気性を有する植毛製品の製造方法として、実公
昭50−221号公報、特公昭53−1770号公報等
に記載されているように接着層を発泡状態に保つ方法が
とられつつある。ところがこの方法に於いて、使用され
る接着剤の条件として実公昭50−221号公報によれ
ば、使用される接着剤(エマルジョン)は55〜60%
以上の固形分を有し、そしてその発泡倍率社2倍以下が
好ましいとされている。たしかに、一般的に市販サレテ
イるエマルジョンを発泡し、その状態で接着剤として、
又、コーティング剤として使用した場合、発泡倍率に於
いて、2倍以上に発泡させた場合、強度が著しく低下す
る。又、高濃度で、しかも発泡倍率が高いため発泡させ
たエマルジョンの表面の乾燥性が早くなっているので植
毛性が著しく低下する。さらに、この方法では発泡倍率
が2倍以下のためボリューム感がやや劣り、又、反撥弾
性が不足する等の致命的欠点を有している。Furthermore, even if flannel or double knit with a voluminous feel is used, it is difficult to obtain a flocked product with the desired soft texture. In particular, flannel or double knits with a voluminous feel are very expensive, so the final result is an expensive flocked product that is not suitable. , Japanese Patent Publication No. 53-1770, etc., methods of maintaining the adhesive layer in a foamed state are being adopted. However, in this method, according to Utility Model Publication No. 50-221, the adhesive (emulsion) used is 55 to 60%
It is said that it is preferable to have a solid content of 2 times or less and an expansion ratio of 2 times or less. It is true that commercially available emulsion is foamed and used as an adhesive in that state.
Furthermore, when used as a coating agent, the strength is significantly reduced when the foaming ratio is expanded to 2 times or more. Moreover, since the concentration is high and the foaming ratio is high, the surface of the foamed emulsion dries quickly, resulting in a marked decrease in flocking properties. Furthermore, this method has fatal drawbacks such as the foaming ratio being less than 2 times, which results in a slightly inferior sense of volume, and a lack of rebound resilience.
そこで、本発明者等は、これらの欠点を解消するため、
比較的低温で発泡する発泡性微小球を使用することを見
出し、更には、接着剤の樹脂濃度が55%以下でしかも
発泡倍率を2倍以上にしても、作業性及び植毛堅牢性の
優れた発泡植毛用接着剤を使用する方法を開発した。し
かし、これら微小球使用発泡あるいは接着剤使用・によ
る機械的発泡の2つの方法に於いては、なおそれぞれ次
のような短所があることを見出した。即ち、微小球を使
用する場合は、
(1)通気性のある植毛品を得ることができない。Therefore, in order to eliminate these drawbacks, the inventors of the present invention,
We have discovered the use of foamable microspheres that foam at relatively low temperatures, and have also achieved excellent workability and flocking fastness even when the resin concentration of the adhesive is 55% or less and the foaming ratio is more than double. We have developed a method using foam adhesive for flocking. However, it has been found that these two methods, foaming using microspheres and mechanical foaming using adhesive, each have the following disadvantages. That is, when using microspheres, (1) it is not possible to obtain air-permeable flocked products;
(2)非常にボリューム感のある、又、クッション性を
高度に要求される場合、微小球の使用量をかなり多くし
なければならない。微小球は非常に高価であるためコス
トが高くなり過ぎる傾向がある。(2) When a very voluminous feel or a high level of cushioning properties are required, the amount of microspheres used must be considerably increased. Microspheres are very expensive and therefore tend to cost too much.
ことであり、一方、機械的発泡による場合は、(1)
発泡倍率を非常に高くするため、コーティング塗布量
を一般の場合より多く塗布するようにドクターのゲージ
−厚を大きくする必要がある。On the other hand, in the case of mechanical foaming, (1)
In order to achieve a very high foaming ratio, it is necessary to increase the gauge and thickness of the doctor so that a larger amount of coating can be applied than would normally be the case.
ソノ他コーティングが困難である。Difficult to coat other materials.
(2) 発泡倍率を低くすればコーティングは容易に
なるが、ボリューム感及び反撥弾性が乏しくなる。(2) If the foaming ratio is lowered, coating will be easier, but the volume and rebound will be poor.
ことである。That's true.
かくて、本発明者等は更に引続き検討を重ね、より好適
な植毛製品の形成について鋭意研究を重ねた結果、微小
球を使用し、更に機械的発泡を併用使用することによっ
て上記欠点を解消することが出来ることを見出すに至っ
た。Therefore, the inventors of the present invention have continued to conduct further studies, and as a result of intensive research into the formation of a more suitable hair transplant product, the above-mentioned drawbacks have been resolved by using microspheres and further using mechanical foaming in combination. I came to discover that it is possible.
即ち、使用する接着剤に、比較的低温で発泡する発泡性
微小球を混合分散せしめ、更に機械的に例えばオークス
ミキサ−型あるいはホイパー型にて空気を混入せしめ、
接着剤を泡状態にし、その発泡状態の接着剤を基材にド
クターコート、あるいはロールコート等によって塗布し
、パイルヲ一般によく使用される静電植毛方法にて植毛
し、70〜IOQ℃で予備乾燥をし、次いで120〜1
50℃で熱処理を施し、接着剤層の中の微小球を膨張せ
しめ、接着層が膨張した微小球と空気による連続的発泡
空隙が混在しているボリューム感のある、かつ通気性2
反撥弾性の優れた植毛製品を得たのである−0
かくして、本発明はボリューム感及び反撥弾性のみなら
ず、史に優れた通気性をも有する改善された植毛製品を
提供することを目的とするものである。That is, foamable microspheres that foam at a relatively low temperature are mixed and dispersed in the adhesive used, and air is further mechanically mixed with an oak mixer type or whipper type, and
The adhesive is made into a foam, and the foamed adhesive is applied to the base material by doctor coating or roll coating, flocked using the commonly used electrostatic flocking method, and pre-dried at 70 to IOQ℃. and then 120-1
Heat-treated at 50℃ to expand the microspheres in the adhesive layer, creating a voluminous and breathable product with a mixture of expanded microspheres in the adhesive layer and continuous foam voids made of air.
Thus, it is an object of the present invention to provide an improved flocked product having not only voluminous feel and rebound properties but also excellent air permeability. It is something.
しかして、かかる目的に適合する本発明植毛製品の特徴
は、基材表面に発泡接着層を介して短繊維を植毛してな
る製品であって、14fl記発泡接着層が発泡性物質を
熱可塑性高分子物で包み込んだ発泡性微小球を加熱発泡
させた膨張球と、空気にて泡立てられた機械的発泡によ
る泡を含む一層によ2て形成され、かつ植毛短繊維の基
端が基材面に達することなく発泡接着層上面に固定され
ている点にある。Therefore, the characteristics of the flocked product of the present invention, which is suitable for such purposes, is that it is a product in which short fibers are flocked on the surface of the base material through a foamed adhesive layer, and the foamed adhesive layer 14 fl. It is formed of an expanded sphere made by heating and foaming expandable microspheres wrapped in a polymer, and a second layer containing mechanical foam foamed with air, and the base end of the flocked short fiber is the base material. The point is that it is fixed to the top surface of the foam adhesive layer without reaching the surface.
以下、6更にその具体的な内容について詳述する。The specific contents of Section 6 will be further detailed below.
先ず、前記本発明にいう発泡性微小球とは、内部に発泡
性物質を包み込んだ熱可塑性高分子物からなる比較的低
温で発泡する微小球であり、その典型的な製造方法は、
例えば特公昭42−265.24号公報に詳細に記載さ
れているが、一般にリミテッド、コアレセンス、ポリマ
ライゼイション(Lim1ted 0oalescen
ce Polymerization )として知られ
ている方法により容易に製造することができる・。First, the expandable microspheres referred to in the present invention are microspheres that are made of a thermoplastic polymer encapsulating a foamable substance and foam at a relatively low temperature, and a typical manufacturing method thereof is as follows:
For example, it is described in detail in Japanese Patent Publication No. 42-265.24, but generally limited, coalescence, and polymerization
ce Polymerization).
ここで、発泡微小球を構成する熱可塑性高分子物として
は、ポリスチレン、ポリメタクリル酸エステル、ポリ塩
化ビニリデン、塩化ビニリデントアクリロニトリルとの
共重合体、アクリロニトリルとアクリル酸メチルとの共
重合体等が通常使用され、また、一方、発泡性物質とし
ては、エチレン、プロパン、ブテン、ネオペンタン、ヘ
キサン。Here, as the thermoplastic polymer constituting the foamed microspheres, polystyrene, polymethacrylic acid ester, polyvinylidene chloride, a copolymer of vinylidene chloride with acrylonitrile, a copolymer of acrylonitrile and methyl acrylate, etc. Commonly used effervescent substances, on the other hand, include ethylene, propane, butene, neopentane, and hexane.
ヘプタン等の前記熱可塑性高分子物の軟化点以下の沸点
を有する脂肪族炭化水素が使用される。そして、これら
熱可塑性高分子物及び発泡性物質は、使用する接着剤及
び得られる植毛製品の種類等に応じて適宜、選択できる
が、発泡性物質としてはネオペンタン、殻を構成する熱
可塑性高分子物としてはポリ塩化ビニリデン、塩化ビニ
リデンとアクリロニトリルとの共重合体、アクリロニト
リルとアクリル酸メチルとの共重合体が最も好適であ・
ν
る。しかし、これに限られるのでないことは云うまでも
ない。An aliphatic hydrocarbon having a boiling point below the softening point of the thermoplastic polymer, such as heptane, is used. These thermoplastic polymers and foamable substances can be selected as appropriate depending on the adhesive used and the type of flocked product to be obtained. The most suitable materials are polyvinylidene chloride, a copolymer of vinylidene chloride and acrylonitrile, and a copolymer of acrylonitrile and methyl acrylate.
ν. However, it goes without saying that it is not limited to this.
この発泡性微小球の大きさとしては、通常、発泡前の直
径で1〜50ミクロンであるが、効果の面からは2〜1
0ミクロンのものが1好ましい。The size of these expandable microspheres is usually 1 to 50 microns in diameter before foaming, but from the viewpoint of effectiveness, it is
0 micron is preferred.
この発泡性微小球は、後述する接着剤に混入され、加熱
発泡されることによって接着層の発泡を促し、発泡層を
つくると共に、該発泡接着層において膨張した球として
存在し、接着層にボリューム感と、回復弾性を与えてい
る。These expandable microspheres are mixed into the adhesive described later and heated and foamed to promote foaming of the adhesive layer, creating a foamed layer, and exist as expanded spheres in the foamed adhesive layer, giving the adhesive layer volume. It gives a feeling and recovery elasticity.
一方、この膨張球に対し、本発明発泡接着層には、更に
空気にて泡立てられた泡が共存し、植毛製品に通気性を
付与している。この泡は、例えば接着剤のエマルジョン
を機械的手段、例えば泡立装置で泡立てて得られるもの
であり、一般的には連続気泡をなしている。この泡の泡
立て時の発泡倍率は、最初の体積の1.2〜5倍、好ま
しくは、1.5〜3倍である。On the other hand, in contrast to the expanded spheres, the foamed adhesive layer of the present invention further contains bubbles foamed with air, thereby imparting air permeability to the flocked product. This foam is obtained, for example, by foaming an adhesive emulsion by mechanical means, such as a foaming device, and generally has open cells. The expansion ratio of this foam during foaming is 1.2 to 5 times, preferably 1.5 to 3 times, the initial volume.
しかし、発泡倍率は添加する発泡性微小球の量と関係が
あり、発泡性微小球の添加量が2〜3%の場合、発泡倍
率は1.5〜2.5倍が最適である。However, the expansion ratio is related to the amount of expandable microspheres added, and when the amount of expandable microspheres added is 2 to 3%, the expansion ratio is optimally 1.5 to 2.5 times.
そして、この泡立ては通常、前記発泡性微小球を混入配
合した後に行なわれる。This foaming is usually performed after mixing and blending the expandable microspheres.
なお、植毛用に使用される接着剤としては、例れば天然
ゴムラテックス、ニトリルゴム、スチレンゴム、クロロ
プレンゴム、スチレン−ブタジェンゴム、ニトリル−ブ
タジェンゴム等の合成ゴムラテックス、ポリ塩化ビニル
、ポリ塩化ビニリデン、ポリ酢酸ビニール、酢ビ−アク
リロニトリル共重合体、ポリアクリル酸エステル等の合
成樹脂エマルジョンが利用されるが、最も一般的に多く
使用される植毛用接着剤はアクリル酸エステル系である
。時々、合成ラテックス、例えばSBR,NBR等が併
用される。勿論、本発明においては樹脂皮膜がある程度
弾性を有するものであればどの接着剤でも使用可能であ
るが、最も最適な接着剤はアクリル酸エステル系である
。その内でも本発明者等が先に開発した機械的発泡に適
したアクリル系エマルジョンは最も適している。Examples of adhesives used for flocking include synthetic rubber latex such as natural rubber latex, nitrile rubber, styrene rubber, chloroprene rubber, styrene-butadiene rubber, and nitrile-butadiene rubber, polyvinyl chloride, polyvinylidene chloride, Synthetic resin emulsions such as polyvinyl acetate, acetic acid-acrylonitrile copolymer, and polyacrylic ester are used, but the most commonly used adhesive for flocking is acrylic ester. Sometimes synthetic latexes such as SBR, NBR, etc. are used in combination. Of course, in the present invention, any adhesive can be used as long as the resin film has some degree of elasticity, but the most suitable adhesive is an acrylic ester adhesive. Among these, the acrylic emulsion, which was developed by the present inventors and is suitable for mechanical foaming, is the most suitable.
しかして、本発明による植毛製品を得るための植毛方法
は、先ず使用する接着剤、例えばアクリル系エマルジョ
ンに前記発泡性微小球を0.5〜5%、好ましくは1〜
3%加え、攪拌し、均一に分散させる。次に、配合物の
粘度を適度に調整する必要カアルが、一般に植毛用に使
用゛されるアクリル系エマルジョンは、アンモニア水に
より自由に粘度を調整することができる。本発明の場合
、10.000〜l 5,000 cpsの範囲が適し
ている。Therefore, in the hair transplantation method for obtaining the hair transplantation product according to the present invention, firstly, 0.5 to 5%, preferably 1 to 5%, of the expandable microspheres are added to the adhesive used, such as an acrylic emulsion.
Add 3% and stir to evenly disperse. Next, it is necessary to appropriately adjust the viscosity of the formulation, but the viscosity of acrylic emulsions generally used for hair transplantation can be adjusted freely with aqueous ammonia. For the present invention, a range of 10,000 to 15,000 cps is suitable.
粘度調整にあたりその他のミツフナ−を併用することも
可能である。又、強度を一段と向上させる目的で従来よ
りよく使用されているメラミン樹脂(例えば、商品名ス
ミテラpVH3)、尿素樹脂あるいはエポキシ系樹脂、
ウレタン系樹脂等を併用することも可能であり、さらに
時として顔料を添加することも可能である。It is also possible to use other mitsufuners in combination to adjust the viscosity. In addition, melamine resin (for example, product name Sumitera pVH3), urea resin or epoxy resin, which has been commonly used for the purpose of further improving strength,
It is also possible to use a urethane resin or the like in combination, and it is also possible to occasionally add a pigment.
そして、かかる配合、及び粘度調整された接着剤を発泡
状態にするには、公知の方法、例えばオークスミキサ−
型あるいはホイバー型による機械的手段などにて泡立た
せることができる。接着剤の発泡状態を長期間例えば4
8時間以上、少なくとも20時間安定に保たせる目的で
泡安定剤を併用してもよい。かかる泡安定剤としてはオ
レイン酸、ステアリン酸、ラウリル酸等の高級脂肪酸の
アンモニウム塩、ラクリル硫酸ナトリウム、ジアンモニ
ウム−N−アルキルスル7オサクシネート等が挙げられ
る。In order to make the adhesive with such a blend and viscosity adjusted into a foamed state, a known method such as an oak mixer can be used.
It can be foamed by mechanical means such as a mold or a whisker mold. Keep the adhesive in a foamed state for a long period of time, e.g.
A foam stabilizer may be used in combination for the purpose of maintaining stability for 8 hours or more, at least 20 hours. Examples of such foam stabilizers include ammonium salts of higher fatty acids such as oleic acid, stearic acid, and lauric acid, sodium lacryl sulfate, and diammonium-N-alkyl sulfate 7-osuccinate.
本発明による前記接着剤の発泡倍率は最初の体積の1.
2〜5倍であるが、好ましくは1.5〜3倍である。発
泡倍率は前述の通り混合される発泡性微小球の量との関
係があるが、その最適組合せは微小球の量が2〜3%に
対して発泡倍率は1.5〜2.5倍である。この範囲外
の場合、微小球の量が少なく、発泡倍率が低い場合はボ
リューム感1反撥弾性は良好であるが堅牢性に問題があ
る。The expansion ratio of the adhesive according to the present invention is 1.
It is 2 to 5 times, preferably 1.5 to 3 times. As mentioned above, the expansion ratio is related to the amount of foamable microspheres mixed, but the optimal combination is when the amount of microspheres is 2 to 3% and the expansion ratio is 1.5 to 2.5 times. be. Outside this range, if the amount of microspheres is small and the foaming ratio is low, the volume feeling 1 impact resilience is good, but there is a problem in robustness.
次に、発泡状態に保たれた接着剤は公知の塗布方法、例
えばローラーコーティングあるいはドクターコーティン
グ法によって基材表面に塗布される。その時の塗布量は
樹脂固形分として50〜2短繊維が植毛される基材とし
ては、綿、レーヨン等の天然繊維、あるいは再生繊維素
繊維若しくはポリエステル、ポリアミド等の合成繊維の
編織物又は不織布であり、通気性を有するものが使用さ
れる。Next, the foamed adhesive is applied to the surface of the substrate by a known application method, such as roller coating or doctor coating. The amount of coating at this time is 50 to 2 as solid resin content.The base material on which short fibers are flocked is a knitted or nonwoven fabric made of natural fibers such as cotton or rayon, or recycled cellulose fibers or synthetic fibers such as polyester or polyamide. A breathable material is used.
又、植毛される前記短繊維としては、綿、羊毛などの天
然繊維、ポリエステル、ポリアミド、ボ。The short fibers to be flocked include natural fibers such as cotton and wool, polyester, polyamide, and wool.
リアクリロニトリル等の合成繊維を始め、任意の短繊維
であり、その繊度、長さは得られる植毛製品の用途、目
的に応じて適宜、選沢される。It can be any short fiber, including synthetic fibers such as lyacrylonitrile, and its fineness and length are appropriately selected depending on the use and purpose of the flocked product to be obtained.
゛ かくして上記により植毛された基材を乾燥し、接着
剤を発泡状態に保ちつつ硬化させるのτあるが、従来の
植毛加工に於ける乾燥は、先ず第1段階として80℃〜
100℃で3〜8分子備乾燥し、次に第2段階として1
20〜160℃、一般的には140〜150℃で3〜5
分熱処理する。しかし、本発明によれば、予備乾燥の時
、微小球を膨張させない方が好ましいので、予備乾燥は
できるだけ低温で短時間が良い。゛Thus, the flocked base material is dried as described above, and the adhesive is cured while keeping it in a foamed state.However, in the conventional flocking process, drying is performed at 80°C to 80°C as the first step.
Dry at 100℃ for 3 to 8 molecules, then as a second step 1
3-5 at 20-160℃, generally 140-150℃
Heat treatment for minutes. However, according to the present invention, it is preferable not to expand the microspheres during pre-drying, so pre-drying is preferably carried out at as low a temperature as possible for a short time.
熱処理条件においても、120℃の場合は5分まで熱処
理可能であるが、5、分級上熱処理をすると、却ってボ
リュームが低下する。150℃の場合、3分以内の熱処
理が最も好ましい。Regarding the heat treatment conditions, heat treatment can be performed for up to 5 minutes at 120° C., but if heat treatment is performed for classification reasons, the volume will decrease on the contrary. In the case of 150° C., heat treatment within 3 minutes is most preferable.
このようにして得られた植毛製品は接着層の発泡と共に
短繊維パイルが浮き上がり、短繊維は基材面より浮いて
発泡接着層で固定され、従来の植毛製品では得られなか
ったボリューム感のある、反撥弾性のある、更に通気性
に優れた植毛製品である。In the flocked product obtained in this way, the short fiber pile rises as the adhesive layer foams, and the short fibers float above the base material surface and are fixed by the foamed adhesive layer, creating a voluminous feel that cannot be obtained with conventional flocked products. It is a flocked product with rebound resilience and excellent breathability.
添付図面第1図はこのようにして得られた植毛製品の構
成概要を示す図であり、図中、(1)は基材、(2)ハ
該基材(1)表面に層着され、かつ、それ自身の材質に
よって基材(1)に一体に接着された発泡接着層、(3
)は発泡接着層(2)の上面にその基端が固定され、基
材(1)面より離れ、実質的に発泡接着層(2)の、厚
みによって支持された短繊維で、前記発泡接着層(2)
には前述した発泡性物質を熱1可塑性高分子物で包み込
んだ比較的低温で発泡する発泡性微小球の膨張球(4)
と、空気にて泡立てられた機械的発泡による泡(4)が
含まれている。FIG. 1 of the accompanying drawings is a diagram showing an outline of the structure of the flocked product thus obtained, in which (1) is a base material, (2) is a layer deposited on the surface of the base material (1), and a foamed adhesive layer (3) integrally adhered to the base material (1) by its own material.
) is a short fiber whose base end is fixed to the upper surface of the foam adhesive layer (2), is separated from the surface of the base material (1), and is substantially supported by the thickness of the foam adhesive layer (2); Layer (2)
The above-mentioned expandable microspheres (4) are foamable microspheres that foam at a relatively low temperature and are made by wrapping the foamable material in a thermoplastic polymer.
and mechanically foamed foam (4) that is foamed with air.
この上記構造をもつ本発明植毛製品は、その発泡接着層
の存在により前記優れた特性を有し、資材用はもちろん
のこと、衣料用としてもその特色を見出すことができる
ものである。The flocked product of the present invention having the above-mentioned structure has the above-mentioned excellent properties due to the presence of the foam adhesive layer, and can be used not only for materials but also for clothing.
以下、かかる本発明植毛製品の利・点を列挙すれば次の
通りである。The advantages and advantages of the hair transplantation product of the present invention are listed below.
(1)通気性のある、ボリューム感のある、反撥弾性に
富んだ植毛製品が得られる。(1) A flocked product that is breathable, has a voluminous feel, and is rich in rebound elasticity can be obtained.
(2)使用する微小球の量は0.5〜5%、好ましくは
1〜3%と極めて少量でよく、シかも機械的発泡倍率は
1.2〜5倍、好ましくは1.5〜2.5倍と容易に得
られる発泡倍率である。(2) The amount of microspheres used may be as small as 0.5 to 5%, preferably 1 to 3%, and the mechanical expansion ratio may be 1.2 to 5 times, preferably 1.5 to 2. The foaming ratio is easily obtainable at .5 times.
(3)使用する接着剤は濃度が55%以下の一般に市販
されている40〜50%の濃度のエマルジョンが使用で
きる。(3) The adhesive used can be a commercially available emulsion with a concentration of 40 to 50%, which has a concentration of 55% or less.
(4) 接着剤の樹脂皮膜の二次転移点が一10℃以下
、例えば−40℃の柔軟な皮膜を形成する接着剤を使用
してもボリューム感と反撥弾性の保持性が良い。(4) Even if an adhesive that forms a flexible film whose secondary transition point of the adhesive resin film is 110°C or less, for example -40°C, is used, the voluminous feel and rebound resilience are maintained well.
次いで、本発明を更に実施例により具体的に説明する。Next, the present invention will be explained in more detail with reference to Examples.
実 施 例 先ず、次の手法によって発泡微小球の製造を行なった。Example First, foamed microspheres were manufactured by the following method.
攪拌機を備えた耐圧重合反応器に蒸溜水100重量部と
30重量%のコロイド状シリカ分散水(商品名 0at
aliod 触媒化学工業社製)15重量部を仕込んだ
。この混合物にジェタノールアミンとアジピン酸の等モ
ル比から縮合反応にて得られた共重合体の10重量%水
溶液2.5重量部を加えて1粘度約100°′p′/2
5℃の生成物を得た。次に重クロム酸カリウヘ2.5重
量%を含む溶液を1重量部添加し、この水溶液のPHを
塩酸を用いて4に調整した。In a pressure-resistant polymerization reactor equipped with a stirrer, 100 parts by weight of distilled water and 30% by weight colloidal silica dispersion water (trade name 0at) were added.
15 parts by weight of aliod (manufactured by Catalysts Kagaku Kogyo Co., Ltd.) were charged. To this mixture, 2.5 parts by weight of a 10% by weight aqueous solution of a copolymer obtained by a condensation reaction from an equimolar ratio of jetanolamine and adipic acid was added to obtain a viscosity of approximately 100°'p'/2.
A product was obtained at 5°C. Next, 1 part by weight of a solution containing 2.5% by weight of potassium dichromate was added, and the pH of this aqueous solution was adjusted to 4 using hydrochloric acid.
モノマーとして塩化ビニリデン100重量部と発泡性物
質としてネオペンタン20重量部と、触媒として過酸化
ベンゾイルとを用いて油相混合物を調整し、これを10
,000 rpmの速度で回転する攪拌翼で激しく攪拌
しながら、油相混合物を水相に添加した。次いで反応器
を密封して反応混合物を約55℃で24時間維持した。An oil phase mixture was prepared using 100 parts by weight of vinylidene chloride as a monomer, 20 parts by weight of neopentane as a foaming substance, and benzoyl peroxide as a catalyst.
The oil phase mixture was added to the water phase while stirring vigorously with a stirrer blade rotating at a speed of ,000 rpm. The reactor was then sealed and the reaction mixture was maintained at approximately 55° C. for 24 hours.
この反応期間中、絶えず緩やかに攪拌し、反応期間終了
後、反応混合物の温度を室温近くまで低下した。反応混
合物は牛乳に似た白色の外観を呈した。反応混合物を濾
過し微小球を取り出して約30℃の乾燥機で乾燥した。During the reaction period, gentle stirring was continued, and after the reaction period was over, the temperature of the reaction mixture was lowered to near room temperature. The reaction mixture had a white appearance similar to milk. The reaction mixture was filtered and the microspheres were taken out and dried in a dryer at about 30°C.
得られた発泡性微小球は5〜8ミクロンであった。The expandable microspheres obtained were 5-8 microns.
かくして得られた発泡性微小球を用い、引続き次の方法
により植毛製品を製造した。即ち、ブチルアクリレ−ト
ル82.4重量部、アクリロニトリル10重量部、アク
リル酸36重晴部、N−メチロール化アクリルアマイド
4重量部を用い、重合時にポリビニルアルコール(重合
度5009部分歯令化)1重量部を添加して重合踵アク
1ノル系自己増粘型、自己架橋型エマルジョンを作成し
た。Using the thus obtained expandable microspheres, a flocked product was subsequently manufactured by the following method. That is, 82.4 parts by weight of butyl acrylate, 10 parts by weight of acrylonitrile, 36 parts by weight of acrylic acid, 4 parts by weight of N-methylolated acrylamide were used, and 1 part by weight of polyvinyl alcohol (degree of polymerization: 5009 parts) was added during polymerization. was added to prepare a polymerized heel-ac 1-nor type self-thickening and self-crosslinking emulsion.
このエマルジョン(固形分濃度45%)100重量部に
アンモニア水1重量部及び上記方法で製造した発泡性微
小球を夫々1.5,2.3重量部を添加して分散液を調
製した。そして、これらの分散液を泡立装置を用いて1
.5〜3倍に発泡させ、これらの発泡状態の分散液とモ
ス9Aの基布に塗布量250(−で塗布し、0.7デニ
ールX0.7mのレーヨン短繊維を植毛し、100℃で
3分間予備乾燥、更に150℃で3分間熱処理を行い、
本発明植毛製品を作成した。To 100 parts by weight of this emulsion (solid content concentration 45%) were added 1 part by weight of aqueous ammonia and 1.5 and 2.3 parts by weight of the expandable microspheres produced by the above method, respectively, to prepare a dispersion. Then, these dispersions were mixed into 1 ml using a foaming device.
.. The foamed dispersion was applied to a base fabric of Moss 9A at a coating amount of 250 (-), and rayon short fibers of 0.7 denier x 0.7 m were flocked, and the mixture was heated at 100°C for 3 to 3 times. Pre-dried for 3 minutes, then heat treated at 150℃ for 3 minutes,
A flocked product of the present invention was created.
一方、比較のために発泡性微小球を添加しないで同様に
して製造した植毛製品及び泡立装置で発泡させないで同
様にして製造した植毛製品を作成した。On the other hand, for comparison, a flocked product was produced in the same manner without adding foamable microspheres, and a flocked product was produced in the same manner without foaming using a foaming device.
このようにして得たこれら本発明植毛製品及び比較植毛
製品について、次いでボリューム感、剛軟度1反撥弾性
及び通気性を夫々測定したところ゛ 第1表に示す如き
結果を得た。The thus obtained flocked products of the present invention and comparative flocked products were then measured for volume, bending/bending repulsion, and air permeability, respectively, and the results shown in Table 1 were obtained.
なお、上表において「ボリューム感」は厚味測定機で厚
味を測定した値で、測定値の大きい程、ボリューム感が
あると判定した。In addition, in the above table, "volume feeling" is the value measured by a thickness measuring device, and it was determined that the larger the measured value, the more voluminous the feeling.
又、「剛軟度」はJIS L−1079(カンチレバー
法)に準じて測定した値、「反撥弾性」は植毛製品より
巾2cm、長さ15〜20crnの大きさのサンプルを
採取し、このサンプルを第2図の如く折り屈げ、折り屈
げた部分が復元しなくなったときの長さくL)を測定し
た値で、測定値が大きい程、回復性が良いと判定した。In addition, "bending resistance" is a value measured according to JIS L-1079 (cantilever method), and "repulsion elasticity" is a value measured by taking a sample with a width of 2 cm and a length of 15 to 20 crn from a flocked product. was bent as shown in Figure 2, and the length (L) at which the bent part no longer recovered was measured, and it was determined that the larger the measured value, the better the recovery.
上記第1表の結果から明らかな如く、発泡性微小球を添
加せず、泡立装置で泡立てを行なわない比較植毛製品は
、ボリューム感1反撥弾性に劣り、又、通気性も不良で
あり、また発泡性微小球を添加して、泡立装置で泡立て
を行なわない植毛製品はボリューム感及び反撥弾性は優
れているが、通気性は不良である。これらに対して本発
明植毛製品はボリューム感及び反撥弾性に優れ、しかも
通気性の良好な植毛製品であった。As is clear from the results in Table 1 above, the comparative flocked product without the addition of expandable microspheres and without foaming using a foaming device had poor volume, poor rebound, and poor air permeability. In addition, flocked products in which expandable microspheres are added and foaming is not performed using a foaming device have excellent volume and rebound, but have poor air permeability. In contrast, the flocked product of the present invention had excellent volume and rebound properties, and also had good air permeability.
第1図は本発明植毛製品の縦断面図、第2図は植毛製品
の1反撥弾性」1の、測定法の説明図である。
(1)・・−・−・・・・・・基 材。
(2)・・・・−・・・・・・発泡接着層。
(3)・・・・・・・・・短繊維。
(4)・・・・・・・・・・・発泡性微小球が加熱発泡
した膨張球。
(5)・・・・・・・・・・・空気にて泡立てられた泡
。FIG. 1 is a longitudinal cross-sectional view of a flocked product of the present invention, and FIG. 2 is an explanatory diagram of a method for measuring the rebound resilience of the flocked product. (1)・・・・・・・・・・Base material. (2)...--Foamed adhesive layer. (3)・・・・・・・・・Short fiber. (4)......Expanded spheres made of foamable microspheres that are heated and foamed. (5)・・・・・・・・・ Foam created by air.
Claims (1)
なる植毛製品であって、前記発泡接着層は、発泡性物質
を熱可塑性高分子物で包み込んだ発泡性微小球を加熱発
泡させた膨張球と、空気にて泡立てられた泡とを含み、
植毛短繊維の基端は基布面に達することなく、前記発泡
接着層面で固定されていることを特徴とする植毛製品。 2、 発泡性微小球の発泡性物質がネオペンタンである
特許請求の範囲第1項記載の植毛製品。 8、 発泡性微小球の熱可塑性高分子物がポリ塩化ビニ
リデン、塩化ビニリデンとアクリロニトリルとの共重合
体、またはアクリロニトリルとアクリル酸メチルとの共
重合体から選ばれた重合体である特許請求の範囲第1項
又は第2項記載の植毛製4、発泡性微小球の緻が接着剤
の固形分に対して1〜3%である特許請求の範囲第1項
ないし第8項のいずれにか記載の植毛製品。[Scope of Claims] 1. A flocked product in which short fibers are flocked on the surface of a base material via a foam adhesive layer, the foam adhesive layer being a foamed product in which a foamable material is wrapped in a thermoplastic polymer. It contains expanded spheres made by heating and foaming sex microspheres and bubbles whipped with air.
A flocked product characterized in that the base ends of the flocked short fibers do not reach the surface of the base fabric and are fixed on the surface of the foam adhesive layer. 2. The hair flocking product according to claim 1, wherein the foamable substance of the foamable microspheres is neopentane. 8. Claims in which the thermoplastic polymer of the expandable microspheres is a polymer selected from polyvinylidene chloride, a copolymer of vinylidene chloride and acrylonitrile, or a copolymer of acrylonitrile and methyl acrylate. The flocked microspheres according to claim 1 or 2 have a density of 1 to 3% based on the solid content of the adhesive, according to any one of claims 1 to 8. hair transplant products.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17482481A JPS5876252A (en) | 1981-10-31 | 1981-10-31 | Hair implanted product |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17482481A JPS5876252A (en) | 1981-10-31 | 1981-10-31 | Hair implanted product |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5876252A true JPS5876252A (en) | 1983-05-09 |
| JPH0129697B2 JPH0129697B2 (en) | 1989-06-13 |
Family
ID=15985299
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17482481A Granted JPS5876252A (en) | 1981-10-31 | 1981-10-31 | Hair implanted product |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5876252A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6042630U (en) * | 1983-08-31 | 1985-03-26 | 川口 勝巳 | Surface material |
| JP2002264234A (en) * | 2001-03-08 | 2002-09-18 | Toyoda Gosei Co Ltd | Method for manufacturing flocked product |
-
1981
- 1981-10-31 JP JP17482481A patent/JPS5876252A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6042630U (en) * | 1983-08-31 | 1985-03-26 | 川口 勝巳 | Surface material |
| JP2002264234A (en) * | 2001-03-08 | 2002-09-18 | Toyoda Gosei Co Ltd | Method for manufacturing flocked product |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0129697B2 (en) | 1989-06-13 |
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