JPS6384668A - Production of flocked article - Google Patents
Production of flocked articleInfo
- Publication number
- JPS6384668A JPS6384668A JP22607086A JP22607086A JPS6384668A JP S6384668 A JPS6384668 A JP S6384668A JP 22607086 A JP22607086 A JP 22607086A JP 22607086 A JP22607086 A JP 22607086A JP S6384668 A JPS6384668 A JP S6384668A
- Authority
- JP
- Japan
- Prior art keywords
- water
- flocking
- pile
- soluble polymer
- flocked
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000000835 fiber Substances 0.000 claims abstract description 41
- 239000002131 composite material Substances 0.000 claims abstract description 26
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 22
- 239000000463 material Substances 0.000 claims description 9
- 229920006158 high molecular weight polymer Polymers 0.000 claims description 5
- 238000004043 dyeing Methods 0.000 abstract description 12
- 239000000758 substrate Substances 0.000 abstract description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract description 2
- 238000000034 method Methods 0.000 description 22
- 239000000853 adhesive Substances 0.000 description 14
- 230000001070 adhesive effect Effects 0.000 description 14
- -1 polyethylene terephthalate Polymers 0.000 description 11
- 229920001410 Microfiber Polymers 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- 229920000728 polyester Polymers 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000004744 fabric Substances 0.000 description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 description 5
- 239000005020 polyethylene terephthalate Substances 0.000 description 5
- 240000002853 Nelumbo nucifera Species 0.000 description 4
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 244000144992 flock Species 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000012190 activator Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- YXTFRJVQOWZDPP-UHFFFAOYSA-M sodium;3,5-dicarboxybenzenesulfonate Chemical compound [Na+].OC(=O)C1=CC(C(O)=O)=CC(S([O-])(=O)=O)=C1 YXTFRJVQOWZDPP-UHFFFAOYSA-M 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- 238000002054 transplantation Methods 0.000 description 3
- 229920001634 Copolyester Polymers 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 229920002302 Nylon 6,6 Polymers 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 229920002614 Polyether block amide Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 244000309466 calf Species 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000009713 electroplating Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000009981 jet dyeing Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229940072033 potash Drugs 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 235000015320 potassium carbonate Nutrition 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000004673 amino silicone softener Substances 0.000 description 1
- ZRSKSQHEOZFGLJ-UHFFFAOYSA-N ammonium adipate Chemical compound [NH4+].[NH4+].[O-]C(=O)CCCCC([O-])=O ZRSKSQHEOZFGLJ-UHFFFAOYSA-N 0.000 description 1
- 235000019293 ammonium adipate Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920006146 polyetheresteramide block copolymer Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
従来、極細繊維を植毛する方法としては、2成分以上か
らなる複合繊維を用いてパイル原糸となし、これを植毛
した後、少なくとも1成分を溶解除去、又は膨潤分割す
る手段が知られている。[Detailed Description of the Invention] [Industrial Application Field] Conventionally, as a method for flocking ultrafine fibers, a composite fiber composed of two or more components is used to make a pile yarn, and after flocking, at least one component is Means for dissolving and removing or swelling and dividing are known.
しかしながら、これらの方法は1成分の除去、分割には
化学薬品を用いざるを得なかった。例えば特開昭59−
76975に開示されているように海成分としてポリス
チレンを用いる場合は、植毛後にトリクレンにて極細化
処理が必要であり、又、特開昭60−155745に開
示されているように海成分としてナイロン6を用いる場
合は植毛後にギ酸にて極細化処理が必要である。これら
の化学薬品の取扱いは危険性があり、溶解除去のための
特殊な設備が必要である。このため作業者の安全衛生面
および製造コスト面にネックがあった。又、極細化処理
時に化学薬品を使用するために、パイル植毛に使用する
接着剤が劣化したり、膨潤したりして、せっかく植毛し
たパイルが扱けてしまうという宿命的な欠点を有してい
た。したがって、安全かつ安定にフロック加工を行なう
には限界があった。However, these methods require the use of chemicals to remove or divide one component. For example, JP-A-59-
When polystyrene is used as the sea component as disclosed in Japanese Patent Laid-Open No. 155745, it is necessary to perform ultra-fine treatment with trichlene after hair transplantation. When using hair transplantation, ultra-fine treatment with formic acid is required after hair transplantation. Handling these chemicals is dangerous and requires special equipment to dissolve and remove them. This created bottlenecks in terms of worker safety and health and manufacturing costs. In addition, because chemicals are used during the ultra-fine treatment, the adhesive used for pile flocking deteriorates or swells, making it difficult to handle the flocked pile. Ta. Therefore, there is a limit to the ability to safely and stably perform flocking.
本発明者らは、上記欠点のない、フロック加工品の製造
方法について鋭意検討した結果、本発明に到達した。特
に、植毛後の極細化あるいはレンコン用多孔化を、染色
加工と同時に行なうことのできるフロック加工品の製造
方法を提供することを目的とする。The present inventors have arrived at the present invention as a result of intensive studies on a method for manufacturing flocked products that does not have the above-mentioned drawbacks. In particular, it is an object of the present invention to provide a method for producing a flocked product in which the process of making the flock fine after flocking or making it porous for lotus roots can be carried out simultaneously with the dyeing process.
(問題点を解決するための手段〕 本発明は、次の構成を有する。(Means for solving problems) The present invention has the following configuration.
(1)パイル原糸を用いてフロック加工品を製造するに
際して、少なくとも2成分からなり、かつその中の少な
くとも1成分が水溶性の高分子重合体で構成される複合
繊維を該パイル原糸として用い、パイル原糸を基体に植
毛俊、水溶性の高分子重合体を水系にて除去することを
特徴とするフロック加工品の製造方法。(1) When producing flocked products using pile yarn, the pile yarn is a composite fiber consisting of at least two components, of which at least one component is a water-soluble polymer. 1. A method for producing a flocked product, which is characterized by using a pile yarn as a base material, flocking it, and removing a water-soluble high molecular weight polymer in an aqueous system.
以下本発明をさらに詳しく説明する。The present invention will be explained in more detail below.
本発明で言う水溶性高分子重合体とは、溶融紡糸可能な
高分子重合体であり、しかも水または熱水で容易に溶解
できる高分子重合体であれば何でもよく、例えばポリビ
ニルアルコール系ポリマ、水溶性ポリアミド(例えばポ
リエーテルアミド系ポリマ、ポリエーテルエステルアミ
ド系ポリマ)、水溶性ポリエステル(例えば5−スルホ
イソフタル酸ナトリウムの共重合ポリエステル系ポリマ
)などがあるが、製糸性あるいはフロック加工性の点か
らポリエーテルアミド系ポリマおよび5−スルホイソフ
タル酸ナトリウムの共重合ポリエステルが好ましく用い
られる。特に、冷水難溶、熱水可溶型の5−スルホイソ
フタル酸ナトリウムの共重合ポリエステルがフロック加
工用パイル原糸として好適である。The water-soluble polymer referred to in the present invention is a polymer that can be melt-spun and may be any polymer that can be easily dissolved in water or hot water, such as polyvinyl alcohol-based polymer, There are water-soluble polyamides (e.g. polyether amide polymers, polyether ester amide polymers), water-soluble polyesters (e.g. copolyester polymers of sodium 5-sulfoisophthalate), etc., but they have poor spinability or flocking properties. A copolymerized polyester of a polyetheramide-based polymer and sodium 5-sulfoisophthalate is preferably used. In particular, copolyester polyester of sodium 5-sulfoisophthalate, which is sparingly soluble in cold water and soluble in hot water, is suitable as the pile yarn for flocking.
本発明ではパイル原糸としてこれらの水溶性の高分子重
合体を少なくとも1成分に用い、少なくとも2成分以上
の高分子重合体からなる複合繊維として用いる。この複
合繊維の構造は後述のフロック加工後の除去工程におい
て、他方の残存する成分が極細化および/またはシンコ
ン様に多孔化するタイプの複合繊維であれば何でもよく
、例えば海鳥型複合繊維、中空環状型複合繊維、多芯型
複合繊維、繊維断面が木目状、モザイク状、放射状、サ
イドバイサイド状複合繊維など用いられる。In the present invention, these water-soluble high molecular weight polymers are used as at least one component of the pile yarn, and are used as composite fibers consisting of at least two or more high molecular weight polymer components. The structure of this composite fiber may be any type of composite fiber as long as the other remaining component becomes ultra-fine and/or porous like a shincon in the removal process after flocking described later, such as seabird type composite fiber, hollow Ring-shaped composite fibers, multifilament composite fibers, and composite fibers with fiber cross sections that are wood grain-like, mosaic-like, radial, or side-by-side are used.
特にフロック加工用パイル原糸として海島型複合繊維が
好適である。In particular, sea-island composite fibers are suitable as pile yarns for flocking.
本発明で用いる複合繊維の伯の成分は、溶融紡糸を行な
い複合繊維としフロック加工後の水溶性高分子重合体の
除去工程で極細繊維および/またはレンコン様多孔化繊
維となりうる高分子重合体、言いかえれば霜維形成能を
有する高分子重合体がよい。例えばナイロン6、ナイロ
ン66、ナイロン12、共重合ナイロン、ポリフェニル
スルホンアミドなどのポリアミド、ポリエチレンテレフ
タレート、共重合ポリエチレンフタレート、ポリブチレ
ンフタレート、共重合ポリブチレンテレフタレートなど
のポリエステル、ポリエチレン、ポリプロピレンなどの
ポリオレフィンなどが用いられる。特にフロック加工用
パイル原糸としてはナイロン6、ナイロン66、ポリエ
チレンテレフタレート、共重合ポリエチレンテレフタレ
ートが好適である。The main component of the composite fiber used in the present invention is a polymer that can be melt-spun into composite fibers and turned into ultrafine fibers and/or lotus root-like porous fibers in the step of removing the water-soluble polymer after flocking. In other words, a high molecular weight polymer having the ability to form frost fibers is preferable. For example, nylon 6, nylon 66, nylon 12, copolymerized nylon, polyamides such as polyphenylsulfonamide, polyesters such as polyethylene terephthalate, copolymerized polyethylene phthalate, polybutylene phthalate, copolymerized polybutylene terephthalate, polyolefins such as polyethylene, polypropylene, etc. is used. In particular, nylon 6, nylon 66, polyethylene terephthalate, and copolymerized polyethylene terephthalate are suitable as the pile yarn for flocking.
複合繊維の繊度は1デニ一ル以上100デニール以下が
好ましい。特に好ましくは3デニ一ル以上20デニール
以下がよい。1デニ一ル未満では繊維か細すぎて電気植
毛性に劣り、100デニールを越えると太すぎて電気植
毛での飛翔性に問題が生ずる。複合繊維から水溶性高分
子重合体を除去した後の繊維の形態として大きく分ける
と極細繊維とレンコン様多孔繊維の2形態に分れる。前
者の場合は柔軟性となめらかなタッチをしたフロック加
工品を創造する。後者の場合は、ミクロクレータ−をフ
ロック加工品の表面に持つため極細繊維と異なった吸い
つくようなタッチと吸水、吸湿性を持つフロック加工品
を創造する。これらはいずれも複合繊維を介して初めて
可能となるものであり、複合繊維の価値を如実に物語る
ものである。水溶性高分子重合体の除去後の極細繊維の
太さは0.5デニール以下が好ましい。0.5デニール
を越えると、極細繊維の持つしなやかさが失われる。The fineness of the composite fiber is preferably 1 denier or more and 100 denier or less. Particularly preferably, it is 3 deniers or more and 20 deniers or less. If the fiber is less than 1 denier, the fibers will be too thin and the electro-flocking property will be poor, and if it exceeds 100 denier, the fiber will be too thick and there will be a problem with the flightability in electro-flocking. After the water-soluble polymer is removed from the composite fibers, the fibers can be roughly divided into two types: ultrafine fibers and lotus root-like porous fibers. In the former case, create flocked products that are flexible and smooth to the touch. In the latter case, the surface of the flocked product has micro-craters, creating a flocked product that has a sticky touch, water absorption, and hygroscopicity that are different from those of ultrafine fibers. All of these things are only possible through composite fibers, and clearly demonstrate the value of composite fibers. The thickness of the ultrafine fiber after removal of the water-soluble polymer is preferably 0.5 denier or less. If it exceeds 0.5 denier, the suppleness of ultrafine fibers will be lost.
複合繊維中における水溶性高分子重合体の比は5重間%
以上、80重量%以下である。5重M%未満では低すぎ
て残存成分の島合流等が発生しやすくなる。一方、80
重尾%を越えると除去成分が多くなり、水溶性高分子重
合体を除去した後のフロック加工品の表面品位が粗とな
り、かつ、コスト的にも不利である。海鳥型複合繊維の
島数は好ましくは4以上である。4未満では極細繊維の
特徴を発揮できず、複合繊維としての価値が低い。The ratio of water-soluble polymer in the composite fiber is 5%
The content is 80% by weight or less. If it is less than 5% by weight, it is too low and the remaining components tend to merge into islands. On the other hand, 80
Exceeding the weight ratio increases the amount of components to be removed, and the surface quality of the flocked product after removing the water-soluble polymer becomes rough, which is also disadvantageous in terms of cost. The number of islands in the seabird type composite fiber is preferably 4 or more. If it is less than 4, the characteristics of an ultrafine fiber cannot be exhibited, and its value as a composite fiber is low.
又、複合繊維に捲縮を付与してもかまわないが、捲縮を
付与せずに使用する方が、フロック加工性の点から好ま
しい。Further, although the composite fiber may be crimped, it is preferable to use it without crimping from the viewpoint of flocking property.
本発明において。フロック加工用パイル原糸をカットす
る前に接着剤おるいは外側のポリマーの融点以上での熱
処理により接着して複合繊維を束状に極太化して使用す
ることもできる。更には、水溶性ポリマを除去すること
により、極細化される複合繊維とレンコン様多孔化複合
繊維を混合して使用することもできる。In the present invention. Before cutting the pile yarn for flocking, it is also possible to bond it with an adhesive or heat treatment at a temperature higher than the melting point of the outer polymer to make the conjugate fibers extremely thick in the form of a bundle. Furthermore, by removing the water-soluble polymer, it is also possible to use a mixture of a conjugate fiber that is made ultra-fine and a lotus root-like porous conjugate fiber.
次に、フロック加工品の製造方法についてで述べる。Next, a method for manufacturing flocked products will be described.
先ず、前記複合繊維のフロック加工用パイル原糸は、従
来公知の方法で適当な長さに切断される。First, the flocking pile yarn of the composite fiber is cut into an appropriate length by a conventionally known method.
カットパイルの長さは、複合繊維の太さ、水溶性高分子
重合体除去後の極細繊維の太さ、そして、カットパイル
の植毛条件等によって決まるが、好ましくは、0.5s
以上、30rnm以下、より好ましくは10mm以下で
ある。0.5mm未満ではパイル長が短すぎてほとんど
接む剤層にめり込んでしまい、極細繊維の効果が発現さ
れにくく、30mmを越えるとパイルが倒れてしまい、
かつ植毛しても扱けやすくなりフロック加工品としての
品位が低下する。該パイルを植毛前に非イオン系活性剤
○有水溶液で精練した後、ケイ酸ソーダ、コロイダルシ
リカ、イソプロピルホスフェートカリよりなる処理液で
処理し、脱水、乾燥などを行なうことも本発明に含まれ
る。次に本発明のパイルを植毛する基体としては織布、
不織布、繊維集合体と樹脂とからなるシート状物質、高
分子物質よりなるシート状物質、人工の皮革様シート状
物質、金属箔、木材板、無機質からなるシート状物質な
ど多くのものが用いられる。The length of the cut pile is determined by the thickness of the composite fiber, the thickness of the ultrafine fiber after removing the water-soluble polymer, the flocking conditions of the cut pile, etc., but is preferably 0.5 seconds.
Above, it is 30 nm or less, more preferably 10 mm or less. If the pile length is less than 0.5 mm, the pile length is too short and almost sinks into the contacting agent layer, making it difficult to express the effect of the ultrafine fibers, and if it exceeds 30 mm, the pile will collapse.
Moreover, even if flocked, it becomes easy to handle and the quality as a flocked product deteriorates. The present invention also includes scouring the pile with an aqueous solution of a nonionic activator before flocking, and then treating it with a treatment solution consisting of sodium silicate, colloidal silica, and isopropyl phosphate potash, and performing dehydration, drying, etc. . Next, as a substrate on which the pile of the present invention is flocked, woven fabric,
Many materials are used, including nonwoven fabrics, sheet materials made of fiber aggregates and resins, sheet materials made of polymeric materials, artificial leather-like sheet materials, metal foils, wood boards, and sheet materials made of inorganic materials. .
次に本発明のパイルと基体を接着する接着剤としては、
フロック加工後の水溶性高分子重合体の除去処理におい
であるいは染色仕上加工処理において耐えうるちのであ
れば何でもよいが、加工性の点からエーテル型おるいは
エステル型ポリウレタンが好ましく用いられる。Next, as the adhesive for bonding the pile and the base of the present invention,
Any polyurethane may be used as long as it can withstand the water-soluble polymer removal treatment after flocking or the dyeing finishing treatment, but ether type or ester type polyurethane is preferably used from the viewpoint of processability.
接着剤を塗布した基体に本発明のパイルを植毛する方法
としては、従来公知の方法が用いられる。Conventionally known methods can be used to flock the pile of the present invention onto a substrate coated with an adhesive.
特にアップ方式による電気植毛が好ましく用いられる。In particular, electric flocking using the up method is preferably used.
次に、本発明のポイントである水溶性高分子重合体の除
去方法について述べる。該水溶性高分子重合体の除去は
水系で行なうことができる。しかし、除去効率向上のた
めに弱アルカリ性水溶液にて処理してもかまわない。更
に、最も好ましい方法としては染色と同時に水溶性高分
子重合体を除去することである。このように、除去成分
として水溶性高分子重合体を用いることにより、通常の
熱水により除去成分を容易に除去することができる。し
かも特別に設備を設ける必要もなく染色工程中に染色と
同時に除去することができるため、安全衛生上の問題も
なくコスト的にも有利であり、しかも有機溶剤や強アル
カリを使用しないため接着剤が劣化したり、膨潤したり
しないので植毛したバイルガ復けてしまうといった問題
も大幅に軽減できるのである。従来、本工程は除去成分
としてポリエチレンを用いた場合はトルエンにて、ポリ
スチレンを用いた場合はトリクレンにて、ポリエステル
を用いた場合は高濃度のアルカリを用いて行なわれてい
たために、染色工程とは別に処理工程が必要であり、か
つ、処理に当っては安全衛生環境上の設備が必要であっ
た。安全上においても、コスト的にも問題が多いのであ
る。更には、有機溶剤あるいは強アルカリで処理するた
めに基体にパイルを接着している接着剤が膨潤したり、
接着剤そのものが劣化したりして植毛したパイルが央け
てしまうという問題も解消できる。Next, a method for removing water-soluble polymers, which is the key point of the present invention, will be described. The water-soluble polymer can be removed in an aqueous system. However, treatment with a weakly alkaline aqueous solution may be used to improve removal efficiency. Furthermore, the most preferred method is to remove the water-soluble polymer at the same time as dyeing. As described above, by using a water-soluble polymer as the removal component, the removal component can be easily removed using ordinary hot water. Moreover, there is no need to install special equipment and it can be removed at the same time as dyeing during the dyeing process, so there are no health and safety issues and it is advantageous in terms of cost.Furthermore, since no organic solvents or strong alkalis are used, adhesives can be removed at the same time as dyeing. Since the hair does not deteriorate or swell, the problem of hair transplanted hair moths coming back undone can be greatly reduced. Conventionally, this process was carried out using toluene when polyethylene was used as the component to be removed, trichlene when polystyrene was used, and highly concentrated alkali when polyester was used. A separate treatment process was required, and treatment required equipment for safety, health, and the environment. There are many problems in terms of safety and cost. Furthermore, the adhesive that adheres the pile to the substrate may swell due to treatment with organic solvents or strong alkalis.
It also solves the problem of the flocked pile becoming curly due to deterioration of the adhesive itself.
以下に実施例により本発明をさらに詳細に説明するが、
本発明をより明確にするものであって、本発明はこれに
限定されるものではない。実施例において、部および%
とあるのは特に記載のないかぎり重量に関するものであ
る。The present invention will be explained in more detail with reference to Examples below.
This makes the present invention more clear, and the present invention is not limited thereto. In the examples, parts and %
References herein refer to weight unless otherwise specified.
実施例1
水溶性高分子重合体としてテレフタル酸61゜2モル%
、イソフタル酸26.3モル%、5−ナトリウムスルホ
イソフタル112.5モル%からなる共重合ポリエステ
ルを海成分とし、ポリエチレンテレフタレートを島成分
として従来公知の海島型口金を用いて溶融紡糸を行ない
、海成分比10%、島成分比90%、席数36島、繊度
10.5dの未延伸糸を得た。次いで65°Cの液浴に
て3゜5倍に延伸し繊度3dのフロック加工用パイル原
糸を得た。紡糸、延伸とも加工上の問題もなく順調に加
工することができた。得られた原糸を1m1Tlにカッ
トし、このカットパイルを非イオン系活性剤含有水溶液
で精練した後、゛ケイ酸ンーダ、コロイダルシリカ、イ
ンプロピルホスフェートカリよりなる処理液に浸漬処理
し、脱水、乾燥した後、電気植毛用パイルとした。この
パイルの表面電気漏洩抵抗は2X108Ω・Cmで必っ
た。 植毛する基布としてポリエステル65%、レーヨ
ン35%の混紡平織物(目付120g/T112)を用
い、その表面に接着剤としてポリエーテル型ポリウレタ
ンDMF溶液(固形分26.5%、10万CpS 72
5°C)を300g/m2となるようにナイフコータで
塗布し、アップ法電植M/Cで植毛した(電圧3万■、
電極間距離10Cm)。該パイルの飛翔性には何の問題
もなく、良好に植毛処理を完了した。パイルの植毛密度
は140C1/m2であった。Example 1 Terephthalic acid 61.2 mol% as a water-soluble polymer
A copolymerized polyester consisting of 26.3 mol% of isophthalic acid and 112.5 mol% of 5-sodium sulfoisophthalate was used as a sea component, and polyethylene terephthalate was used as an island component, and melt spinning was performed using a conventionally known sea-island type spinneret. An undrawn yarn having a component ratio of 10%, an island component ratio of 90%, a seat count of 36 islands, and a fineness of 10.5 d was obtained. Next, the yarn was stretched 3.times.5 times in a liquid bath at 65.degree. C. to obtain pile yarn for flocking with a fineness of 3 d. Both spinning and stretching were successfully processed without any processing problems. The obtained yarn was cut into 1 m 1 Tl, and after scouring the cut pile with an aqueous solution containing a nonionic activator, it was immersed in a treatment solution consisting of sodium silicate, colloidal silica, and inpropyl phosphate potash, dehydrated, After drying, it was made into a pile for electric flocking. The surface electrical leakage resistance of this pile was 2×10 8 Ω·Cm. A blended plain fabric of 65% polyester and 35% rayon (fabric weight 120g/T112) is used as the base fabric for flocking, and a polyether type polyurethane DMF solution (solid content 26.5%, 100,000 CpS 72) is used as an adhesive on the surface.
5°C) to 300g/m2 using a knife coater, and flocked with an up-method electroplating M/C (voltage 30,000cm,
distance between electrodes 10 cm). There were no problems with the flying properties of the pile, and the flocking process was successfully completed. The flocking density of the pile was 140C1/m2.
植毛後120℃で乾燥し、ついでサーキュラ型液流染色
機で海成分の除去と染色を処理温度120′Cにて同時
に行ない、還元洗浄後、アミノシリコン系柔軟剤を付与
(トーレシリコン(株)SM−8702)して仕上げた
。得られたフロック加工品は0.075dの極細の短い
パイルが緻密にしっかりと植毛されたカーフスェード調
のものであった。植毛密度は120g/m2でおり、接
着剤の膨潤もなく染色工程でのパイルの脱落はほとんど
見られなかった。After flocking, it is dried at 120°C, then the sea component is removed and dyed at the same time using a circular jet dyeing machine at a processing temperature of 120'C, and after reduction cleaning, an amino silicone softener is applied (Toray Silicon Co., Ltd.) SM-8702) and finished. The obtained flocked product had a calf suede appearance, with extremely fine short piles of 0.075 d being densely and tightly flocked. The flocking density was 120 g/m2, and there was no swelling of the adhesive and almost no pile was observed to fall off during the dyeing process.
比較例1
海成分にポリスチレンを用いた以外は実施例1と同様の
加工を電気植毛まで行ない、次いで、トリクレンにより
海成分の除去を行なった後は実施例1と同様に染色仕上
加工を行なった。このものの植毛密度は105g/Tn
2であり、実施例1と比較して表面品位が劣り商品価値
の低いものであった。また、海成分除去にトリクレンを
使用するため接着剤の膨潤が起こり、パイルの脱落が見
られ脱海装置の掃除に過大の時間を浪費した。更には、
脱海の溶剤としてトリクレンを使用するために、特殊な
設備が必要となり、かつ、安全衛生面においても多大な
経費が余儀なくされた。Comparative Example 1 The same processing as in Example 1 was performed up to electric flocking, except that polystyrene was used for the sea component, and then, after the sea component was removed with Trichlorine, the dyeing and finishing process was performed in the same manner as in Example 1. . The flocking density of this item is 105g/Tn
2, the surface quality was inferior to that of Example 1, and the commercial value was low. In addition, the use of trichlene to remove sea components caused the adhesive to swell, resulting in piles falling off and excessive time being wasted cleaning the sea removal equipment. Furthermore,
The use of trichlene as a solvent for sea removal required special equipment, and also required a large amount of expense in terms of safety and health.
実施例2
N−6: 20%1、N−66: 20%、ポリエチレ
ングリコールジアンモニュームアジベート:60%から
なる共重合ポリアミドを海成分とし、ポリエチレンテレ
フタレートを島成分として従来公知の海島型口金を用い
て溶融紡糸を行ない、海成分比15%、島成分比85%
、席数70島、繊度13,5dの未延伸糸を得た。次い
で120℃の熱板にて2.7倍に延伸し繊度5dのフロ
ック加工用パイル原糸を得た。得られた原糸を1,51
T1mにカットし、非イオン系活性剤含有水溶液で精練
した後、脱水、乾燥し、フロック加工用パイル原糸とし
た。このパイルの表面電気漏洩抵抗は1゜5X108Ω
・cmでめった。Example 2 A conventionally known sea-island type cap with a copolyamide consisting of N-6: 20% 1, N-66: 20%, and polyethylene glycol diammonium adipate: 60% as a sea component and polyethylene terephthalate as an island component. The sea component ratio is 15% and the island component ratio is 85%.
An undrawn yarn having a number of seats of 70 and a fineness of 13.5 d was obtained. Then, it was stretched 2.7 times on a hot plate at 120° C. to obtain a pile fiber for flocking with a fineness of 5 d. The obtained raw yarn is 1,51
The fibers were cut to a length of T1m, scoured with an aqueous solution containing a nonionic activator, dehydrated, and dried to obtain pile fibers for flock processing. The surface electrical leakage resistance of this pile is 1゜5X108Ω
・I missed it in cm.
植毛する基布としてポリエステル65%、レーヨン35
%の混紡平織物(目付120Q/m2)を用い、その表
面に接着剤としてポリエステル型ポリウレタンDMF溶
液(固形分25%、9万cps/25°C)を300g
/Tr12となるようにナイフコータで塗布し、アップ
法電植M/Cで植毛した(電圧3万■、電極間距離10
Cm)。該パイルの飛翔性には何の問題もなく、良好に
植毛処理を完了した。パイルの植毛密度は200 CI
/ Tr12であった。植毛後120℃で乾燥し、つ
いでサーキュラ型液流染色機で海成分除去と染色を処理
温度100℃にて同時に行ない、還元洗浄後、アミンシ
リコン系柔軟剤を付与して仕上げた。得られた植毛布(
フロック加工品)は0.061dの極細の短いパイルが
緻密にしっかりと植毛されたカーフスェード調のもので
めった。植毛密度は165Q/Tr12であり、接着剤
の膨潤もなく染色工程でのパイルの脱落はほとんど見ら
れなかった。65% polyester, 35% rayon as the base fabric for flocking
% blended plain weave fabric (basis weight 120Q/m2) was used, and 300g of polyester-type polyurethane DMF solution (solid content 25%, 90,000 cps/25°C) was applied to the surface as an adhesive.
/Tr12 using a knife coater and flocking with an up-method electroplating M/C (voltage 30,000 mm, distance between electrodes 10
Cm). There were no problems with the flying properties of the pile, and the flocking process was successfully completed. The flocking density of the pile is 200 CI
/Tr12. After flocking, it was dried at 120°C, and then sea component removal and dyeing were simultaneously carried out using a circular jet dyeing machine at a processing temperature of 100°C. After reduction washing, an amine silicone softener was applied to finish. The obtained flocked cloth (
The flocked product) is a calf suede-like material with 0.061 d of ultra-fine short pile that is densely and tightly flocked. The flocking density was 165Q/Tr12, and there was no swelling of the adhesive and almost no pile was observed to fall off during the dyeing process.
(発明の効果)
本発明はパイル原糸に少なくとも1成分が水溶性高分子
重合体からなる複合繊維を用いるので下記効果が得られ
る。(Effects of the Invention) Since the present invention uses composite fibers in which at least one component is a water-soluble polymer as the pile yarn, the following effects can be obtained.
(1)水系除去が可能となり、従来の安全衛生、作業環
境などの問題が一挙に解消する。(1) Water-based removal becomes possible, and conventional problems such as safety, health, and working environment are solved at once.
(2)水溶性高分子重合体の除去を染色と同時に行なう
ことが可能となり、工程省略によるトータルコストの著
しい低下が図れる。(2) It becomes possible to remove the water-soluble polymer at the same time as dyeing, and the total cost can be significantly reduced by omitting the process.
(3) 接着剤が膨潤、溶解することがないので、植
毛後のパイルの生えぎわがしつかりし、植毛パイルの脱
落がほとんどない。(3) Since the adhesive does not swell or dissolve, the edges of the pile after flocking are firm and there is almost no chance of the flock falling off.
(4) このため接着剤の使用量の軽減や、利用範囲
の拡大が図れる。(4) Therefore, the amount of adhesive used can be reduced and the scope of use can be expanded.
(5) 得られる加工品は、植毛パイルの緻密性、柔
軟性、均一性、表面品位、耐久性が向上する。(5) The resulting processed product has improved flocked pile density, flexibility, uniformity, surface quality, and durability.
Claims (1)
際して、少なくとも2成分からなり、かつその中の少な
くとも1成分が水溶性の高分子重合体で構成される複合
繊維を該パイル原糸として用い、パイル原糸を基体に植
毛後、水溶性の高分子重合体を水系にて除去することを
特徴とするフロック加工品の製造方法。(1) When producing flocked products using pile yarn, the pile yarn is a composite fiber consisting of at least two components, of which at least one component is a water-soluble polymer. 1. A method for producing a flocked product, which comprises using a pile yarn as a base material and then removing a water-soluble high molecular weight polymer in an aqueous system.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22607086A JPS6384668A (en) | 1986-09-26 | 1986-09-26 | Production of flocked article |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22607086A JPS6384668A (en) | 1986-09-26 | 1986-09-26 | Production of flocked article |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6384668A true JPS6384668A (en) | 1988-04-15 |
| JPH0262313B2 JPH0262313B2 (en) | 1990-12-25 |
Family
ID=16839338
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22607086A Granted JPS6384668A (en) | 1986-09-26 | 1986-09-26 | Production of flocked article |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6384668A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8733075B2 (en) * | 2005-10-17 | 2014-05-27 | Welspun India Limited | Hygro materials for use in making yarns and fabrics |
| US9152122B2 (en) | 2011-05-30 | 2015-10-06 | Canon Finetech Inc. | Static-electricity-blocking mounting unit and electronic apparatus |
| US9828704B2 (en) | 2015-09-10 | 2017-11-28 | Welspun India Limited | Terry article with synthetic filament yarns and method of making same |
-
1986
- 1986-09-26 JP JP22607086A patent/JPS6384668A/en active Granted
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8733075B2 (en) * | 2005-10-17 | 2014-05-27 | Welspun India Limited | Hygro materials for use in making yarns and fabrics |
| US10287714B2 (en) | 2005-10-17 | 2019-05-14 | Welspun India Limited | Hygro materials for use in making yarns and fabrics |
| US9152122B2 (en) | 2011-05-30 | 2015-10-06 | Canon Finetech Inc. | Static-electricity-blocking mounting unit and electronic apparatus |
| US9828704B2 (en) | 2015-09-10 | 2017-11-28 | Welspun India Limited | Terry article with synthetic filament yarns and method of making same |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0262313B2 (en) | 1990-12-25 |
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