JPS6364549B2 - - Google Patents
Info
- Publication number
- JPS6364549B2 JPS6364549B2 JP60024199A JP2419985A JPS6364549B2 JP S6364549 B2 JPS6364549 B2 JP S6364549B2 JP 60024199 A JP60024199 A JP 60024199A JP 2419985 A JP2419985 A JP 2419985A JP S6364549 B2 JPS6364549 B2 JP S6364549B2
- Authority
- JP
- Japan
- Prior art keywords
- nonwoven fabric
- fibers
- fatty acid
- acid amide
- artificial leather
- 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.)
- Expired
Links
- 239000004745 nonwoven fabric Substances 0.000 claims description 53
- 239000000835 fiber Substances 0.000 claims description 36
- 239000000126 substance Substances 0.000 claims description 26
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 19
- 239000000194 fatty acid Substances 0.000 claims description 19
- 229930195729 fatty acid Natural products 0.000 claims description 19
- 150000004665 fatty acids Chemical class 0.000 claims description 19
- 239000002649 leather substitute Substances 0.000 claims description 14
- 229920000642 polymer Polymers 0.000 claims description 12
- 238000004513 sizing Methods 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 9
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 8
- 239000006185 dispersion Substances 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000003292 glue Substances 0.000 claims description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 3
- 229920002472 Starch Polymers 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 3
- 238000004132 cross linking Methods 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 claims description 2
- 229920001038 ethylene copolymer Polymers 0.000 claims description 2
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 2
- 239000011118 polyvinyl acetate Substances 0.000 claims description 2
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 description 17
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 229920002635 polyurethane Polymers 0.000 description 9
- 239000004814 polyurethane Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 7
- 230000015271 coagulation Effects 0.000 description 6
- 238000005345 coagulation Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000002998 adhesive polymer Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- -1 polyethylene terephthalate Polymers 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000002345 surface coating layer Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Nonwoven Fabrics (AREA)
Description
〔利用分野〕
本発明は人工皮革の基材用不織布の加工に関す
る。更に詳しくは、柔軟性に優れ、かつ腰のある
人工皮革の製造に適した不織布の加工に関するも
のである。
〔従来技術〕
人工皮革は絡合不織布に弾性高分子物質を含浸
した基体と、その基体表面に高分子物質の被覆層
を付与した銀付製品、あるいは基体をバフ掛けし
て繊維立毛層を形成したスエード調製品が作られ
ている。そして人工皮革の風合いを柔軟なものと
する手段として、不織布にあらかじめシリコーン
樹脂で処理した後、高分子物質を含浸することに
より繊維と含浸高分子物質との接着を防ぐ方法
(特公昭45―33797号公報)、含浸高分子物質とは
溶剤を異にする糊剤高分子物質を不織布に含浸
し、不織布繊維の一部を被覆あるいは繊維空間の
一部を充填し、弾性高分子物質を含浸・凝固した
後、糊剤高分子物質を除去して繊維と弾性高分子
物質との間に空隙を形成せしめる方法(例えば特
公昭45―18745号公報、特開昭49―109697号公報)
などが提案されている。
〔解決しようとする問題点〕
しかし、これら公知の方法では、不織布繊維の
化学構造によつて糊剤高分子物質との親和性が悪
く、十分な被覆効果が得られないとか、あるいは
処理液と繊維との濡れ特性の関係で不織布繊維の
表面に付着して繊維と含浸高分子物質との離型作
用を十分に発揮することは難かしい等の欠点を有
している。従つて、これら公知の方法で得られる
人工皮革の基体は風合いが硬くなり、折り曲げに
対してもボキボキした挫屈した折れしわ形態にな
る。本発明者等は、そうした欠点を解決し、腰が
あり柔軟な人工皮革を製造するため鋭意検討を重
ねた結果、本発明に至つた。
〔発明の目的〕
本発明は、柔軟性で腰があり、外観の良い、更
に、二次加工性や着用性に優れた人工皮革を製造
するに適した基材用加工不織布を提供するにあ
る。
〔発明の構成〕
本発明は、人工皮革用基布として適した不織布
であつて、糊剤高分子物質と、次式(1)で示した脂
肪酸アマイドとを不織布繊維に付着せしめたもの
である。
R1CONR3(R2NR3)oOCR1 ……(1)
(但し、R1=炭素数12〜28のアルキル基
R2=炭素数1〜8のアルキレン基
R3=Hあるいは分子間架橋結合
n=1〜8の数)
〔問題点の解決手段〕
本発明は、前述したように、糊剤高分子物質と
前記脂肪酸アマイドとを不織布繊維に付着せしめ
た不織布であるが、本発明で適用される不織布
は、天然繊維、再生繊維または合成繊維からなる
ものであるが、好ましくはポリエステル繊維、ポ
ルアミド繊維、ポリオレフイン繊維、アクリル系
繊維などの合成繊維を主体にした繊維をカードに
掛けてウエブにした乾式法、あるいは水に分散さ
せて抄紙法でウエブにした湿式法によつて作つた
ウエブをニードルパンチ法あるいは流体噴射法な
どの手段で絡合した繊維絡合不織布である。これ
ら繊維絡合不織布は人工皮革用基体としての適性
の点で好ましい。
不織布に付着せしめる糊剤高分子物質は、後の
工程で含浸する弾性高分子物質の溶剤または分散
剤たとえばポリウレタンや天然または合成ゴムの
溶剤または分散剤とは異なる溶剤に溶解する高分
子物質が好ましく、例えばポリビニルアルコー
ル、部分ケン化ポリビニルアルコール、カルボキ
シメチルセルロース(Na塩)、ポリ酢酸ビニル、
酢酸ビニル―エチレン共重合体、殿粉、ポリエス
テル、変性デンプン、変性セルロース等水、アル
コール類またはアセトンなどに可溶な糊剤高分子
物質が好ましい。特に水溶性の糊剤高分子、すな
わちポリビニルアルコール系ポリマー、カルボキ
シメチルセルロース、殿粉等が好ましい。
また不織布に付着せしめる糊剤高分子物質の繊
維に対する付着量は2〜40重量%である。付着量
が少ないと後工程で含浸する弾性高分子物質が繊
維の交叉部に多く付着し、繊維間を固定してしま
い、風合いの硬いものにしてしまうとか、あるい
は後工程の加工に適した面の平滑な不織布が得ら
れないとか、更には後工程での加工において不織
布の形態が変化するなどの問題を生ずる。一方、
付着量が多いと、糊剤高分子物質の凝固時に生ず
るマイグレーシヨンで不均一付着状態を生じ、人
工皮革の性能上にも好ましくない影響をもたら
す。
次に、併用する脂肪酸アマイドは、例えば次の
ような化学構造のものがある。
C15H31CONH(CH2NH)6OC15H31 (1)
C17H35CONH(C4H8NH)3OC23H47 (2)
C13H27CONH(C6H12NH)4OC13H27 (3)
これら脂肪酸アマイドは水あるいはアルコール
類に溶解または分散状態にして使用するか、ある
いは水中分散物を加温して溶解し、水中油滴状に
して使用するのが好ましい。
また、不織布に付着せしめる脂肪酸アマイドの
繊維に対する付着量は0.5〜13重量%である。付
着量が少ないと、後工程で含浸する弾性高分子物
質と繊維との接着防止効果が小さい。更に、不織
布を熱プレス等で表面を平滑化したり、厚みの均
一化したりする場合にも、作業性が悪く、面のき
れいなものが得られない。一方、付着量が多い場
合には糊剤高分子物質の凝固時に脱落してしまい
損失量になるだけである。
そして、糊剤高分子物質と脂肪酸アミドを不織
布に付着せしめる方法は、それぞれを別々の処理
で付着させてもよいが、糊剤高分子物質の溶液ま
たは分散液に脂肪酸アミドの溶液または分散液を
混合した場合、いずれかの物質の凝集が生じなけ
れば混合系で同時処理を行うことが好ましい。処
理した不織布には付着物を繊維に固着させるため
の凝固処理を施こす。凝固法は、特別の方法を要
しない通常の方法で行えばよいが、脂肪酸アミド
を繊維表面に比較的均一に付着させるためには、
最終不織布加工工程までの間に100〜150℃程度の
加温処理が加わることが好ましい。
糊剤高分子物質および脂肪酸アミドを付着せし
めた不織布に対して、必要に応じて平滑面を有す
るロール、ベルト面に密着せしめて熱処理あるい
は加圧熱処理を行うと、平滑面を有し、厚みむら
の少ない加工不織布とすることができる。
次に本発明の実施態様を具体的に説明するが、
本発明はこれらの実施例に限定されるものではな
い。なお、本文中の部および%はことわりのない
限り重量に関するものである。
実施例 1〜6
繊度1.3デニールのポリエチレンテレフタレー
ト(以下PEHとする)繊維のランダムウエブを
作り、4枚積層してニードルパンチを行つて平均
目付285g/m2の絡合不織布を作つた。
一方、絡合不織布の繊維に糊付け加工を行う糊
剤組成物として、ケン化度98%のポリビニルアル
コール4部、次式で示した脂肪酸アマイドを用
い、
脂肪酸アマイド10%乳化分散液を表1に示した割
合で配合し、水に溶解分散させた組成液を調整し
た。
[Field of Application] The present invention relates to the processing of nonwoven fabrics for base materials of artificial leather. More specifically, the present invention relates to the processing of nonwoven fabrics that have excellent flexibility and are suitable for producing stiff artificial leather. [Prior art] Artificial leather consists of a base made of entangled nonwoven fabric impregnated with an elastic polymeric substance, and a silver-plated product with a coating layer of a polymeric substance applied to the surface of the base, or a fiber napped layer is formed by buffing the base. Made from soft suede. As a means to make the texture of artificial leather soft, a method is proposed in which nonwoven fabric is treated with silicone resin in advance and then impregnated with a polymeric substance to prevent adhesion between the fibers and the impregnated polymeric substance (Japanese Patent Publication No. 45-33797). (No. Publication), a nonwoven fabric is impregnated with a sizing polymeric substance that uses a different solvent from the impregnated polymeric substance, and a part of the nonwoven fabric fibers is covered or a part of the fiber space is filled, and an elastic polymeric substance is impregnated. After coagulation, the adhesive polymeric substance is removed to form voids between the fibers and the elastic polymeric substance (for example, Japanese Patent Publication No. 18745-1970, Japanese Patent Application Laid-Open No. 109697-1987).
etc. have been proposed. [Problems to be solved] However, with these known methods, the chemical structure of the nonwoven fabric fibers has poor affinity with the adhesive polymer, and a sufficient coating effect cannot be obtained, or the processing liquid Due to its wetting properties with the fibers, it has the disadvantage that it is difficult to adhere to the surface of the nonwoven fibers and to sufficiently exhibit the mold release effect between the fibers and the impregnated polymeric material. Therefore, the artificial leather substrates obtained by these known methods have a hard feel, and even when bent, they have a buckled and wrinkled shape. The inventors of the present invention have conducted intensive studies to overcome these drawbacks and produce artificial leather that is firm and flexible, and as a result, they have arrived at the present invention. [Object of the invention] The present invention provides a processed nonwoven fabric for a base material that is flexible, has good elasticity, has a good appearance, and is suitable for producing artificial leather that has excellent secondary processability and wearability. . [Structure of the Invention] The present invention is a nonwoven fabric suitable as a base fabric for artificial leather, in which a sizing polymer substance and a fatty acid amide represented by the following formula (1) are attached to nonwoven fabric fibers. . R 1 CONR 3 (R 2 NR 3 ) o OCR 1 ...(1) (However, R 1 = Alkyl group with 12 to 28 carbon atoms R 2 = Alkylene group with 1 to 8 carbon atoms R 3 = H or intermolecular Cross-linking (number of n=1 to 8) [Means for solving the problem] As described above, the present invention is a nonwoven fabric in which a sizing agent polymer substance and the fatty acid amide are attached to nonwoven fabric fibers. The nonwoven fabrics used in this process are made of natural fibers, recycled fibers, or synthetic fibers, but preferably synthetic fibers such as polyester fibers, polyamide fibers, polyolefin fibers, acrylic fibers, etc. are used as the main fibers. It is a fiber-entangled nonwoven fabric made by making a web by a dry method, or by a wet method by dispersing it in water and making a web by a paper-making method, and then entangling it by means such as a needle punch method or a fluid jet method. These fiber-entangled nonwoven fabrics are preferred in terms of their suitability as substrates for artificial leather. The adhesive polymeric substance to be attached to the nonwoven fabric is preferably a polymeric substance that dissolves in a solvent different from the solvent or dispersant for the elastic polymeric substance to be impregnated in a later step, such as the solvent or dispersant for polyurethane or natural or synthetic rubber. , such as polyvinyl alcohol, partially saponified polyvinyl alcohol, carboxymethyl cellulose (Na salt), polyvinyl acetate,
Preferred are polymeric sizing agents that are soluble in water, alcohols, or acetone, such as vinyl acetate-ethylene copolymer, starch, polyester, modified starch, and modified cellulose. Particularly preferred are water-soluble sizing polymers, such as polyvinyl alcohol polymers, carboxymethyl cellulose, starch, and the like. Further, the amount of the adhesive polymeric material attached to the nonwoven fabric on the fibers is 2 to 40% by weight. If the amount of adhesion is small, the elastic polymer substance impregnated in the later process will adhere to the intersections of the fibers, fixing the fibers, resulting in a hard texture, or a surface that is not suitable for processing in the later process. Problems arise, such as not being able to obtain a smooth nonwoven fabric, and furthermore, the shape of the nonwoven fabric changing during processing in subsequent steps. on the other hand,
If the amount of adhesion is large, migration that occurs during coagulation of the sizing agent polymer substance will result in non-uniform adhesion, which will also have an unfavorable effect on the performance of the artificial leather. Next, the fatty acid amide used in combination has, for example, one having the following chemical structure. C 15 H 31 CONH (CH 2 NH) 6 OC 15 H 31 (1) C 17 H 35 CONH (C 4 H 8 NH) 3 OC 23 H 47 (2) C 13 H 27 CONH (C 6 H 12 NH) 4 O C 13 H 27 (3) It is preferable to use these fatty acid amides in a dissolved or dispersed state in water or alcohol, or to dissolve the dispersion in water by heating and use the fatty acid amide in the form of oil-in-water droplets. Further, the amount of fatty acid amide attached to the fibers to be attached to the nonwoven fabric is 0.5 to 13% by weight. If the amount of adhesion is small, the effect of preventing adhesion between the fiber and the elastic polymer substance impregnated in the subsequent process will be small. Furthermore, even when the surface of the nonwoven fabric is smoothed or the thickness is made uniform by hot pressing or the like, the workability is poor and a clean surface cannot be obtained. On the other hand, if the amount of adhesion is large, the adhesive will fall off when the adhesive polymer solidifies, resulting in a loss. As for the method of attaching the sizing polymer substance and the fatty acid amide to the nonwoven fabric, each may be applied in separate treatments, but a solution or dispersion of the fatty acid amide is added to the solution or dispersion of the sizing polymer substance. When mixed, it is preferable to carry out simultaneous processing in a mixed system unless aggregation of any substance occurs. The treated nonwoven fabric is subjected to a coagulation process to fix deposits to the fibers. The coagulation method can be carried out by a normal method that does not require any special method, but in order to adhere the fatty acid amide relatively uniformly to the fiber surface, it is necessary to
It is preferable to add a heating treatment at about 100 to 150° C. before the final nonwoven fabric processing step. If a nonwoven fabric to which a sizing agent polymer substance and a fatty acid amide are attached is heat-treated or pressurized while being brought into close contact with a roll or belt surface having a smooth surface as necessary, the non-woven fabric will have a smooth surface and will have an uneven thickness. It is possible to create a processed nonwoven fabric with less. Next, embodiments of the present invention will be specifically explained.
The present invention is not limited to these examples. Note that parts and percentages in the text refer to weight unless otherwise specified. Examples 1 to 6 A random web of polyethylene terephthalate (hereinafter referred to as PEH) fiber with a fineness of 1.3 denier was made, and four sheets were laminated and needle punched to make an entangled nonwoven fabric with an average basis weight of 285 g/m 2 . On the other hand, as a sizing agent composition for gluing the fibers of the entangled nonwoven fabric, 4 parts of polyvinyl alcohol with a degree of saponification of 98% and a fatty acid amide represented by the following formula were used. A 10% fatty acid amide emulsion dispersion was blended in the proportions shown in Table 1 and dissolved and dispersed in water to prepare a composition.
【表】
この調整した組成液を、上記絡合不織布に対し
て約200%の絞り率になるように絞液し、120℃の
熱風乾燥機で大部分を乾燥し、次いで鏡面を有す
る熱ドラム乾燥機に表面を接触させて乾燥を完結
させ表面の平滑な糊付け不織布を得た。
次にポリエステル系ソフトセグメントのポリウ
レタン18%のジメチルホルムアミド(DMFとす
る)溶液に凝固調節剤および着色剤を添加した含
浸液を糊付け不織布中に含浸飽充し、更に不織布
の平滑化した面に、厚さ0.8mmの割当てを当てて
表面被覆層を付与した後、DMF水溶液中に浸漬
して凝固させ、続いて88〜90℃の熱水中でポリビ
ニルアルコールを溶解除去し、そして乾燥した。
ポリウレタンを含浸・塗布して得たシート状物の
裏面側をスライスして、厚さ1.7mmのシート状物
とした。このシート状物を握つたときの風合い、
表面被覆層を内側にして折り曲げた折れしわ、シ
ートを10%両方向に引張して生ずる表面のモヤモ
ヤした凹凸感など、商品として重要な感覚的性能
および、繊維とポリウレタンとの接着性を観察
し、その結果を表2に示した。[Table] Squeeze this adjusted composition liquid to the above entangled nonwoven fabric to a squeezing rate of approximately 200%, dry most of it in a hot air dryer at 120°C, and then dry it in a heated drum with a mirror surface. The surface was brought into contact with a dryer to complete drying and a glued nonwoven fabric with a smooth surface was obtained. Next, the glued nonwoven fabric was fully impregnated with an impregnating solution containing 18% polyurethane of the polyester soft segment in dimethylformamide (DMF) to which a coagulation regulator and a coloring agent were added. After applying a surface coating layer with a thickness of 0.8 mm, it was immersed in a DMF aqueous solution to solidify, followed by dissolving and removing the polyvinyl alcohol in hot water at 88-90°C, and drying.
The back side of the sheet obtained by impregnating and applying polyurethane was sliced to obtain a sheet having a thickness of 1.7 mm. The texture of this sheet-like object when you hold it,
We observed the sensorial performance that is important for a product, such as the creases caused by folding the sheet with the surface coating layer on the inside, and the fuzzy, uneven feel of the surface caused by pulling the sheet 10% in both directions, as well as the adhesion between the fiber and polyurethane. The results are shown in Table 2.
【表】
すなわち、本発明品は繊維とその後に付与する
ポリウレタンとがよく離れるため、特に感覚的性
能に優れたものになり、このシート状物に表面着
色、型押し等の仕上げを行つた製品を、靴に加工
すると、履き心地の良い靴となつた。
実施例 7
繊度0.7デニール、36mmのPET非収縮繊維50部
と繊度1.5デニール、51mmのPET収縮性繊維50部
を混綿して作つたクロスラツプウエブをニードル
パンチして、平均目付170g/m2の絡合不織布を
作り、95℃の熱水中に浸漬して、収縮処理を行
い、面積収縮率46%の収縮絡合不織布を作つた。
一方、ポリビニルアルコール7部、次式で示し
た脂肪酸アマイドを用い、
脂肪酸アマイド15%乳化分散液を7部および水86
部の割合で配合した組成液を調整した。
この調整した糊剤組成液を上記収縮不織布に含
浸し、絞液して付着率145%の糊剤組成液を含む
収縮不織布を作り、次いで平滑面をした熱ドラム
乾燥機に表面を接触させて乾燥し、表面の平滑な
糊付け不織布を得た。
次に、ポリテトラメチレンエーテル/ポリカプ
ロラクトンソフトセグメント混合系ポリウレタン
18%DMF溶液に凝固調節剤及び着色剤を添加し
た含浸液を上記糊付け不織布に含浸し、DMF40
%水溶液中で凝固させ、続いて88〜90℃の熱水中
でポリビニルアルコールを溶解除去し、そして乾
燥した。
このようにして得られたシート状物は握つた風
合いが、天然皮革の牛革(キツプ)様に腰があつ
て柔軟な感じを与えるものであり、繊維と含浸ポ
リウレタンとはよく離れており、繊維の交叉部、
接合部もポリウレタンで固められてはいなかつ
た。更に、脂肪酸アマイドは全てが除去されるこ
となく残存し、それも風合いに良い結果をもたら
している。
このシート状物の両面にバフイング仕上げを行
つたところベロア調の製品が得られた。一方、平
滑面側にポリウレタンスポンジ層をのせ、着色、
型押しして仕上げたところ、キヤツプ調の銀付き
製品が得られた。
実施例 8
繊度1.5デニールのナイロン―6繊維70部、繊
度1.5デニールのPET収縮性繊維30部を混綿して
作つた目付約210g/m2のニードルパンチ絡合不
織布を、95℃の熱水中に浸漬して収縮処理を行
い、面積収縮率35%の収縮絡合不織布を作つた。
この収縮不織布に実施例7で調整した糊剤組成
液を含浸し、絞液して付着率140%の糊剤組成液
を含む収縮不織布を作り、乾燥して糊付け不織布
を得た。この糊付け不織布に実施例7と同じウレ
タン加工を行なつて得たシート状物は天然皮革の
牛革(グローブ革)様の柔軟な感じを与えるもの
であつた。[Table] In other words, the product of the present invention has particularly excellent sensory performance because the fibers are well separated from the polyurethane applied afterwards, and the product is a sheet-like product that has been finished with surface coloring, embossing, etc. When processed into shoes, they became comfortable shoes. Example 7 A cross-lap web made by blending 50 parts of PET non-shrinkable fiber with a fineness of 0.7 denier and 36 mm and 50 parts of PET shrinkable fiber with a fineness of 1.5 denier and 51 mm was needle-punched to give an average basis weight of 170 g/m 2 An entangled nonwoven fabric was prepared, and then immersed in hot water at 95°C for shrinkage treatment to produce a shrink entangled nonwoven fabric with an area shrinkage rate of 46%. On the other hand, using 7 parts of polyvinyl alcohol and a fatty acid amide shown by the following formula, 7 parts of fatty acid amide 15% emulsified dispersion and 86 parts of water
A composition solution was prepared by blending the ingredients in the following proportions: This adjusted size composition liquid was impregnated into the above-mentioned shrinkable nonwoven fabric, and the liquid was squeezed out to produce a shrinkable nonwoven fabric containing the size composition liquid with an adhesion rate of 145%, and then the surface was brought into contact with a hot drum dryer with a smooth surface. After drying, a glued nonwoven fabric with a smooth surface was obtained. Next, polytetramethylene ether/polycaprolactone soft segment mixed polyurethane
The above glued nonwoven fabric was impregnated with an impregnating solution containing a 18% DMF solution with a coagulation regulator and a colorant added, and the DMF40
% aqueous solution, followed by dissolving and removing the polyvinyl alcohol in hot water at 88-90°C, and drying. The sheet-like material obtained in this way has a firm and flexible feel similar to that of natural cowhide leather, and the fibers and the impregnated polyurethane are well separated and the the intersection of
The joints were also not sealed with polyurethane. Furthermore, the fatty acid amide remains without being completely removed, which also has a good effect on the texture. When a buffing finish was applied to both sides of this sheet-like product, a velor-like product was obtained. On the other hand, a polyurethane sponge layer is placed on the smooth side and colored.
When finished by stamping, a cap-like silver-plated product was obtained. Example 8 A needle-punched entangled nonwoven fabric with a basis weight of approximately 210 g/m 2 made by blending 70 parts of nylon-6 fiber with a fineness of 1.5 denier and 30 parts of PET shrinkable fiber with a fineness of 1.5 denier was soaked in hot water at 95°C. A shrinkage-entangled nonwoven fabric with an area shrinkage rate of 35% was produced by immersing it in water and performing a shrinkage treatment. This shrinkable nonwoven fabric was impregnated with the glue composition liquid prepared in Example 7, squeezed to produce a shrinkable nonwoven fabric containing the glue composition liquid with an adhesion rate of 140%, and dried to obtain a glued nonwoven fabric. A sheet-like product obtained by subjecting this pasted nonwoven fabric to the same urethane treatment as in Example 7 had a soft feel similar to that of natural cowhide (glove leather).
Claims (1)
の表面に存在している糊剤および次式(1)で示され
る脂肪酸アマイドからなる人工皮革用不織布。 R1CONR3(R2NR3)oOCR1 ……(1) (但し、R1=炭素数12〜28のアルキル基 R2=炭素数1〜8のアルキレン基 R3=Hあるいは分子間架橋結合 n=1〜8の数) 2 糊剤高分子物質が、ポリビニルアルコール、
部分ケン化ポリビニルアルコール、カルボキシメ
チルセルロース(Na塩)、ポリ酢酸ビニル、酢酸
ビニル―エチレン共重合体、殿粉から選ばれた少
なくとも1種類である特許請求の範囲第1項記載
の人工皮革用不織布。 3 糊剤高分子物質および脂肪酸アマイドの不織
布繊維に対する付着量が、糊剤高分子物質は2〜
40重量%、脂肪酸アマイドは0.5〜13重量%の範
囲である特許請求の範囲第1項記載の人工皮革用
不繊布。 4 糊剤高分子物質溶液または分散液に、次式(1)
で示される脂肪酸アマイドの溶液または分散液を
添加した組成液を不織布に含浸し、凝固して、上
記組成物を不織布繊維に付着せしめることを特徴
とする人工皮革用不織布の製造法。 R1CONR3(R2NR3)oOCR1 ……(1) (但し、R1=炭素数12〜28のアルキル基 R2=炭素数1〜8のアルキレン基 R3=Hあるいは分子間架橋結合 n=1〜8の数)[Scope of Claims] 1. A nonwoven fabric for artificial leather comprising a nonwoven fabric, a sizing agent present on the surface of fibers constituting the nonwoven fabric, and a fatty acid amide represented by the following formula (1). R 1 CONR 3 (R 2 NR 3 ) o OCR 1 ...(1) (However, R 1 = Alkyl group with 12 to 28 carbon atoms R 2 = Alkylene group with 1 to 8 carbon atoms R 3 = H or intermolecular Cross-linking (n = number of 1 to 8) 2 The glue polymer substance is polyvinyl alcohol,
The nonwoven fabric for artificial leather according to claim 1, which is at least one selected from partially saponified polyvinyl alcohol, carboxymethyl cellulose (Na salt), polyvinyl acetate, vinyl acetate-ethylene copolymer, and starch. 3. The adhesion amount of the sizing polymer substance and fatty acid amide to the nonwoven fabric fibers is 2 to 2.
40% by weight, and the fatty acid amide content is in the range of 0.5 to 13% by weight. The nonwoven fabric for artificial leather according to claim 1. 4 Add the following formula (1) to the glue polymer substance solution or dispersion.
1. A method for producing a nonwoven fabric for artificial leather, which comprises impregnating a nonwoven fabric with a solution or dispersion of a fatty acid amide represented by the following formula and solidifying the composition to adhere the composition to the nonwoven fabric fibers. R 1 CONR 3 (R 2 NR 3 ) o OCR 1 ...(1) (However, R 1 = Alkyl group with 12 to 28 carbon atoms R 2 = Alkylene group with 1 to 8 carbon atoms R 3 = H or intermolecular cross-linking n=number of 1 to 8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60024199A JPS61186570A (en) | 1985-02-11 | 1985-02-11 | Nonwoven fabric for artificial leather and its production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60024199A JPS61186570A (en) | 1985-02-11 | 1985-02-11 | Nonwoven fabric for artificial leather and its production |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61186570A JPS61186570A (en) | 1986-08-20 |
JPS6364549B2 true JPS6364549B2 (en) | 1988-12-12 |
Family
ID=12131648
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60024199A Granted JPS61186570A (en) | 1985-02-11 | 1985-02-11 | Nonwoven fabric for artificial leather and its production |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61186570A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4367874B2 (en) * | 2000-01-24 | 2009-11-18 | 竹本油脂株式会社 | Synthetic fiber treatment agent for carbon fiber production and method for treating synthetic fiber for carbon fiber production |
JP2011174193A (en) * | 2010-02-24 | 2011-09-08 | Unitika Ltd | Polylactic acid-based filament nonwovwn fabric |
JP5657916B2 (en) * | 2010-05-19 | 2015-01-21 | ユニチカ株式会社 | Non-woven |
CN113227489B (en) | 2018-12-27 | 2023-06-06 | 株式会社可乐丽 | Vertical wool artificial leather and manufacturing method thereof |
-
1985
- 1985-02-11 JP JP60024199A patent/JPS61186570A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS61186570A (en) | 1986-08-20 |
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