JPS616376A - Production of suede like artificial leather - Google Patents
Production of suede like artificial leatherInfo
- Publication number
- JPS616376A JPS616376A JP60072487A JP7248785A JPS616376A JP S616376 A JPS616376 A JP S616376A JP 60072487 A JP60072487 A JP 60072487A JP 7248785 A JP7248785 A JP 7248785A JP S616376 A JPS616376 A JP S616376A
- Authority
- JP
- Japan
- Prior art keywords
- item
- fiber
- base fabric
- water
- fibers
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000002649 leather substitute Substances 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000000835 fiber Substances 0.000 claims description 38
- 239000004744 fabric Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 27
- 239000004745 nonwoven fabric Substances 0.000 claims description 25
- 230000000694 effects Effects 0.000 claims description 24
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 15
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 15
- 229920003169 water-soluble polymer Polymers 0.000 claims description 15
- 239000003292 glue Substances 0.000 claims description 10
- 238000004513 sizing Methods 0.000 claims description 10
- 229920001410 Microfiber Polymers 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000006185 dispersion Substances 0.000 claims description 5
- 229920002472 Starch Polymers 0.000 claims description 4
- 239000000853 adhesive Substances 0.000 claims description 4
- 230000001070 adhesive effect Effects 0.000 claims description 4
- 229920003225 polyurethane elastomer Polymers 0.000 claims description 4
- 239000008107 starch Substances 0.000 claims description 4
- 235000019698 starch Nutrition 0.000 claims description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- 229920002125 Sokalan® Polymers 0.000 claims 1
- 239000001768 carboxy methyl cellulose Substances 0.000 claims 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 239000004584 polyacrylic acid Substances 0.000 claims 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims 1
- 229920002635 polyurethane Polymers 0.000 description 17
- 239000004814 polyurethane Substances 0.000 description 17
- 239000007864 aqueous solution Substances 0.000 description 9
- 239000010985 leather Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- 239000013013 elastic material Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 238000004080 punching Methods 0.000 description 5
- 238000007598 dipping method Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000004026 adhesive bonding Methods 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 206010035039 Piloerection Diseases 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 238000009998 heat setting Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 230000005371 pilomotor reflex Effects 0.000 description 2
- -1 polyethylene terephthalate Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 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
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 206010016654 Fibrosis Diseases 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229920006184 cellulose methylcellulose Polymers 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 238000009990 desizing Methods 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000004761 fibrosis Effects 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/04—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (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】
発明の分野
本発明は表面効果に優れたスェード調人工皮革の製造方
法に関する。さらに詳しくは、本発明は、指でこすった
場合、その表面に、これに応じた色調の変化を生ずる。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a method for producing suede-like artificial leather with excellent surface effects. More specifically, the present invention produces a corresponding change in tone on the surface when rubbed with a finger.
いわゆるライティング効果を備えたスェード調の人工皮
革の製造方法に関する。This invention relates to a method of manufacturing suede-like artificial leather with a so-called lighting effect.
発明の背景
スェード皮(5uede )は、特有の優れた表面効果
を有する。ここで表面効果とは、スェード独特の表面特
性のうちライティング効果(writingeffec
t ) を意味し、スェードを指でこすった場合、こ
すった方向へ表面の毛羽か向き、周囲とは異なる色が表
われ、色調に差異が生することを言う。このようなライ
ティング効果が生するためには、特定の繊度、0.5デ
ニール以下の極細繊維でなければならないことは勿論表
面毛羽の密度が高密度であり、同時に一定の長さの毛羽
長を持たなけれはならず、基布に充填されている高分子
弾性体と繊維との間に適当な間隔、空隙が形成されなけ
れはならない。BACKGROUND OF THE INVENTION Suede leather (5uede) has unique and excellent surface effects. Here, the surface effect refers to the writing effect, which is one of the surface characteristics unique to suede.
t) means that when you rub suede with your fingers, the fuzz on the surface turns in the direction of the rubbing, resulting in a different color from the surrounding area, resulting in a difference in tone. In order to produce such a lighting effect, the fibers must have a specific fineness and be 0.5 denier or less, and the density of the surface fluff must be high, and at the same time, the fluff must have a certain length. Appropriate spacing and voids must be formed between the fibers and the polymeric elastic material filled in the base fabric.
従来のスェード調人工皮革は、不織布に高分子弾性体を
含浸付与した後、適当な前処理なしにバフィングするた
め、毛羽の長さが一定しなかったり、立毛密度が低く天
然スェードのような優雅な製品を得にくいのが実情であ
った。Conventional suede-like artificial leather is made by impregnating a nonwoven fabric with a polymeric elastic material and then buffing it without proper pretreatment, so the length of the fluff is inconsistent, the density of the raised pile is low, and it is not as elegant as natural suede. The reality is that it is difficult to obtain a product that is suitable for the market.
特1乙スェード製品は立毛により製品の評価か大きく左
右され、その用途がしばしば制限されるため、多(の皮
革研究者はその解決のため繊維高分子弾性体表面加工方
法など種々の側面から研究を推進してきた。Special 1: The evaluation of suede products is greatly influenced by the nap, and its uses are often limited. To solve this problem, many leather researchers are conducting research from various aspects, such as surface processing methods for fiber polymer elastic materials. has been promoted.
例えば米国特許第4.206.267号などではポリビ
ニルアルコールのような水溶性高分子物質を不織布に含
浸付与して高分子−511i性体を充填した後、再びポ
リビニルアルコールを除去することによって繊維と高分
子弾性体の間に空隙を形成する。For example, in U.S. Pat. No. 4,206,267, a nonwoven fabric is impregnated with a water-soluble polymer substance such as polyvinyl alcohol to fill it with a polymer-511i substance, and then the polyvinyl alcohol is removed again to form fibers. A void is formed between the polymer elastic bodies.
しかし結局空隙が充分ではなかったり、あるいは基布の
表面部であいかわらず繊維と高分子弾性体が工程中に結
合する可能性か存在する。また、特公昭48−7700
1号公報では皮革のソート物の表面を塩化亜鉛水溶液な
どて処理して高分子弾性体及び繊維を適当に脆化させて
バフィング性を向上させる方法を開示しているが、かか
る方法では処理液か布の中央部まで浸透して布の物性を
大きく低下させる可能性を排除することはできないO
また、特公昭55−32828号公報ではバフィングの
前にシリコン化合物で処理しているが、これでは触感は
良好であるものの立毛が均一でないなどの問題がある。However, there is a possibility that the voids may not be sufficient, or that the fibers and the polymeric elastomer may continue to bond on the surface of the base fabric during the process. In addition, special public service No. 48-7700
Publication No. 1 discloses a method in which the surface of a sorted leather product is treated with an aqueous zinc chloride solution to appropriately embrittle the polymer elastic body and fibers to improve buffing properties. It cannot be ruled out that there is a possibility that the water permeates into the center of the fabric and significantly deteriorates the physical properties of the fabric.Also, in Japanese Patent Publication No. 55-32828, treatment is performed with a silicon compound before buffing; Although the texture is good, there are problems such as uneven napping.
発明の概説
発明者らは人工皮革に適用される高分子弾性体の物性、
及び皮革のシート物に充填された高分子弾性体の分布状
態などを検討した結果、表面ライティング(writi
ng )効果に優れたスェード調人工皮革の製造方法を
完成するに至った。Overview of the invention The inventors have discovered the physical properties of elastic polymers applied to artificial leather,
As a result of examining the distribution of polymeric elastic material filled in leather sheets, we found that surface writing
ng) We have completed a method for producing suede-like artificial leather with excellent effects.
したがって、本発明は、前記のごとき、従来の諸欠点を
除去するために一定条件の不織布を糊付処理した後、再
度、水溶性高分子水溶液、又は分散液を該基布の表面部
に集中的に付与−して、さらにポリウレタン弾性体を充
填した後にバフィングするこCζこよって表面効−果に
優れたスェード調人工皮革の製造方法を提供することを
目的とする。Therefore, in order to eliminate the various drawbacks of the conventional fabric as described above, the present invention applies a pasting treatment to a nonwoven fabric under certain conditions, and then again concentrates a water-soluble polymer aqueous solution or dispersion on the surface of the base fabric. The object of the present invention is to provide a method for manufacturing suede-like artificial leather which has excellent surface effects by adding a polyurethane elastomer and buffing it after being filled with a polyurethane elastomer.
ずなわち、本発明は、極細繊維化か可能な繊度5デニー
ル以下の繊維からなる不織布を水溶性高分子を糊剤とし
て第1段の糊付処理を行ない基布とした後、再度水溶性
高分子水溶液、又は分散液を該基布の表面部に集中的)
こイ:1与して第2段の糊付処理を行ない、さらにポリ
ウレタン弾性体を充t口した後、前記水溶性高分子を除
去しバフィングすることを特徴とする表面効果に優れた
スェード調人工皮革の製造方法である。That is, in the present invention, a nonwoven fabric made of fibers with a fineness of 5 denier or less that can be made into ultra-fine fibers is subjected to a first sizing treatment using a water-soluble polymer as a sizing agent to form a base fabric, and then the nonwoven fabric is made into a water-soluble Concentrate the polymer aqueous solution or dispersion on the surface of the base fabric)
A suede-like material with excellent surface effect, characterized in that the second step of gluing treatment is carried out by applying 100% polyurethane, and then the water-soluble polymer is removed and buffing is carried out. This is a method for manufacturing artificial leather.
発明の詳細 な説明を詳細に説明すると次のようである。Details of the invention The detailed explanation is as follows.
本発明は最終製品にて繊度が05デニール以下に分割し
うる海・島型繊維を使用して高密度不織布全成形し、つ
いて公知のポリビニルアルコールなどの水溶性高分子物
を含浸付与した後、ここに再びポリビニルアルコールを
主体とする塗布可能な粘度を有する溶液、又は分散液を
塗布して、基布の表面部に高分子弾性体が充填される可
能性を種棒的に排除することにより、その後のパフイン
ク性を著しく向−Lさせ、表面ライティング効果に優れ
たスェード調人工皮革を製借する方法である。In the present invention, a high-density nonwoven fabric is entirely formed using sea/island type fibers that can be divided into fineness of 0.5 denier or less in the final product, and then impregnated with a known water-soluble polymer such as polyvinyl alcohol. By again applying a solution or dispersion mainly composed of polyvinyl alcohol with a coatable viscosity to eliminate the possibility that the surface of the base fabric is filled with the polymeric elastic material. This is a method of producing suede-like artificial leather that has significantly improved subsequent puff ink properties and has an excellent surface writing effect.
ここでバフィング性というのはバフィング工程による立
毛発現効果を意味するものでライティング効果と直結す
る概念を持っている。Buffing property here refers to the piloerection effect caused by the buffing process, and has a concept that is directly connected to the lighting effect.
5デニール以下の繊維でできたニードルパンチング(n
eedle punching )不織布にポリビニル
アルコールのような水溶性高分子を含浸させると、−次
的に繊維−繊維間の交絡点に付着し、バインダー(bi
nder )効果か現われるため形態安定性か寿られ、
且つ繊維とポリウレタンの間に空隙を形成して基布を柔
軟にし、表面のバフィング性を高めるのみならす、糊n
後、細lJ&維化vIJ下をする時にフィブリル(fi
b口1)の集束性を高めるなど多くの効果か期待される
。Needle punching (n
When a water-soluble polymer such as polyvinyl alcohol is impregnated into a nonwoven fabric (eedle punching), it then adheres to the fiber-to-fiber intertwining points and forms a binder (eedle punching).
nder) form stability or longevity in order for the effect to appear,
In addition, it forms voids between the fibers and polyurethane, softens the base fabric, and improves the buffing properties of the surface.
After that, when lowering the thin IJ & fibrosis vIJ, fibrils
Many effects are expected, such as improving the convergence of the b-port 1).
本発明においては発明目的上バフィング性向上の観点の
みから観察して見る。In the present invention, observations will be made only from the viewpoint of improving buffing properties for the purpose of the invention.
551図に示すごとく、不織布に水溶性高分子を糊付処
理した基布の断面は、繊維と繊維の交絡点+a)及び繊
維の表面(1))に一定の、ヒ?さて糊剤か塗布されて
いる。この糊剤フィルム層の厚さは粘付剤の付5−量、
濃度などによって異なるか、約01〜0.5μの範囲内
で塗布されるのか糊付の目的及び以後の脱糊工程上最も
適当で、ポリビニルアルコールで処理する場合は5〜2
offlki%の水溶液に浸透剤、界面活性剤、柔軟剤
など目的に合った適当な界面活性剤を添加し、これを処
理液として含浸パディングして繊維の重篭に対して固型
分基準t”i15〜20重i%のポリビニルアルコール
ヲ(−1与するのか最もりfましい。As shown in Figure 551, the cross section of the base fabric, which is a nonwoven fabric pasted with a water-soluble polymer, has a certain amount of heat at the fiber-to-fiber intertwining point +a) and at the surface of the fibers (1)). Well, glue has been applied. The thickness of this adhesive film layer is 5 - amount of adhesive applied,
Does it vary depending on the concentration, etc., or is it applied within the range of about 0.01 to 0.5μ?It is most suitable for the purpose of gluing and the subsequent desizing process, and when treated with polyvinyl alcohol, it is applied within the range of about 0.01 to 0.5μ.
A suitable surfactant suitable for the purpose, such as a penetrant, a surfactant, and a softener, is added to an aqueous solution of offflki%, and this is used as a treatment liquid for impregnation and padding, and the solids content is t'' for a heavy basket of fibers. It is most unfortunate that polyvinyl alcohol of 15 to 20% by weight gives (-1).
つぎに、このような糊fI後、水溶性高分子物を処理す
る方法、及びその効果を示す。既存の方法により糊付し
た基布にポリウレタンなどの1高分子弾性体を直接浸す
と、ポリウレタンが基布の厚さ方向に充填される。これ
により基布の表面に繊維とポリウレタンか共存すること
になって、以後のハフインク工程で繊維は一定の良好な
長さで立毛せず、ポリウレタンは自体の強度によって容
易には除去されない。Next, a method of treating a water-soluble polymer after such glue fI and its effects will be described. When a monopolymer elastomer such as polyurethane is directly immersed into a base fabric pasted using an existing method, the polyurethane is filled in the thickness direction of the base fabric. As a result, the fibers and polyurethane coexist on the surface of the base fabric, and the fibers do not stand up to a certain good length in the subsequent huff ink process, and the polyurethane is not easily removed due to its own strength.
従って本発明者らは、糊付布(第2図のc)(こ再Q・
水溶性高分子物を塗布することによって第2図の(d)
のように糊イ:j剤を基布厚の1/2、好ましくは1/
4以内の表面のみに充填するようにしてポリウレタンが
充填される余地を排除し、バフィング性を改良する方法
を考案した。この時の糊付機は第3図に示すように第1
段および第2段糊付最の合刷1が(e)から(f)の間
であるのが皮革の物性面からも最も好ましい。このよう
にすればポリウレタンを脆化させるなどの湧作をせす、
繊維の強度か第4図の(g)〜(h)間の範囲のバフィ
ング性を備え表面ライティング効果に優れたスェード調
人工皮革を製造することができる。Therefore, the present inventors used a starched cloth (FIG. 2 c)
(d) in Figure 2 by applying a water-soluble polymer.
Glue: Add the agent to 1/2 of the thickness of the base fabric, preferably 1/2 of the thickness of the base fabric.
We devised a method to improve buffing properties by filling only the surface within 4 to eliminate the room for polyurethane to be filled. The gluing machine at this time was the first one as shown in Figure 3.
From the viewpoint of the physical properties of the leather, it is most preferable that the number of glued layers 1 of the first step and second step is between (e) and (f). Doing this will cause the polyurethane to embrittle, etc.
It is possible to produce suede-like artificial leather that has fiber strength and buffing properties in the range between (g) and (h) in FIG. 4 and has an excellent surface writing effect.
ここで第1段、第2段糊f=1処理液には、水溶性高置
1かいずれも使用ijJ能であるか、工程りの問題の起
こらないものでなけれはならない。それ故。Here, the first and second stage glues f=1 treatment liquids must be water-soluble and high-temperature 1 or both must be usable or must not cause problems in the process. Therefore.
主ニポリビニルアルコール(IIVA)、カルボキンメ
チルセルロース(c:Mc)、でんぷン、てんふん類加
工品、ポリアクリル酸文びその混合物などが適当な添加
剤とともに調製、使用されてよい。Primarily polyvinyl alcohol (IIVA), carboxyl methyl cellulose (c:Mc), starch, processed starch products, mixtures thereof, etc. may be prepared and used with appropriate additives.
本発明によればパディング(padding ) 時、
樹脂を均一に処理しなけれは、乾燥後、甚しい凹凸の起
こる可能性があるので、特に留意する必要がある。ある
程度的がっても以後のポリウレタン浸漬工程上、別に問
題点はなく熱固定(+1cat−press)などによ
ってこれを解決することもできる。熱固定などをすれば
、不織布表面部の繊維密度が向上1、 Ql 後のパフ
インク性が向−トするという附随的な効果も期待できる
。According to the present invention, when padding,
Unless the resin is treated uniformly, severe unevenness may occur after drying, so special care must be taken. Even if a certain degree of damage occurs, there is no particular problem in the subsequent polyurethane dipping process, and this problem can be solved by heat setting (+1 cat-press) or the like. Heat setting can also be expected to have the additional effects of improving the fiber density on the surface of the nonwoven fabric1 and improving the puff ink properties after Ql.
才な、2段糊付された不織布をついてポリウレタンにて
含aする時には、2段糊付された表面層かステイールV
1−ル(5teel roll )に接触するように、
また凝固槽の下部を通過させた方がよい。When a non-woven fabric with a two-step adhesive is coated with polyurethane, the two-step adhesive surface layer or stay V
1-teel roll (5teel roll)
It is also better to let it pass through the lower part of the coagulation tank.
本発明において不織布を形成する繊維としては5デニー
ル以下の繊度を持つものがいずれも使用”J能であるか
、最終製品においては05デニール以下にならなけれは
良好なライティング効果、触j・3、ウェットタッチ(
wet−touch ) 感などを発揮することかでき
ない。In the present invention, any fiber with a fineness of 5 denier or less is used as the fiber forming the nonwoven fabric.If the fiber has a fineness of 5 denier or less, it must have a fineness of 0.05 denier or less in the final product to have a good lighting effect, tactility J.3, wet touch (
Wet-touch (wet-touch)
このような極細繊維は一定のデニールを持つ連続品分チ
フィラメント集束体の中に繊維高分子物を特殊な形態で
同時に紡糸して、化学的、物理的な後tJa工工程で集
束体を除去すれば繊維品分−ト繊度か05デニールリ、
下の極細繊維となる。These ultra-fine fibers are produced by simultaneously spinning fiber polymers in a special form into a continuous filament bundle with a certain denier, and then removing the bundle through a chemical and physical post-processing process. Then, the fiber item fineness is 05 denier,
This becomes the ultra-fine fibers at the bottom.
使用可能な繊維の種類としてはポリエステル、ポリアミ
ド、ポリアクリロニトリルなど繊維形成能を有する高分
子がいずれも採用しえ、高収縮性、及び潜在巻縮性など
を持つ繊維を使用すれば不織布の密度を高めるのに非常
に効果的である。The types of fibers that can be used include polyester, polyamide, polyacrylonitrile, and other polymers that have fiber-forming ability.If fibers with high shrinkage and latent crimp properties are used, the density of the nonwoven fabric can be reduced. It is very effective in increasing
一方、不織布に充頃する品分子弾性体としてはポリエス
テル系ポリウレタン、ポリエーテル系ポリウレタン、ま
たポリエステル−ポリエーテル共重合ポリウレタンなど
の各種ポリウレタン及びNl5R,110(などの各種
合成ゴム、またこれらを2種以−L混合したものなどが
可能である。本発明においてはポリエステル−ポリエー
テル共重合ポリウレタンが最適であり、繊維かポリエス
テルであればより好ましい。On the other hand, the molecular elastic materials that can be used in nonwoven fabrics include polyester polyurethane, polyether polyurethane, various polyurethanes such as polyester-polyether copolyurethane, various synthetic rubbers such as Nl5R, 110, and two types of these. A mixture of these and other materials is possible.In the present invention, polyester-polyether copolyurethane is most suitable, and fiber or polyester is more preferable.
本発明で使用される不織布を製造するには、上記繊維を
クロス−ラッパー(cross−Iapper ) 、
ランダム−ラッパー(random−1apper )
f;どてウェッブ(web)に製造し、このウェッブ
をニードルパンチングして3次元結合させる方法、抄紙
法などを用いうるが、ニードルパンチングして厚さの方
向に繊維を走向させる方か良好な立毛性を発揮するとい
うへでよい。To produce the nonwoven fabric used in the present invention, the fibers described above are processed into a cross-lapper,
random-1apper
f; It is possible to use a method such as manufacturing a web into a web and needle punching this web to three-dimensionally bond the web, or a paper making method, but it is better to use needle punching to run the fibers in the direction of the thickness. It is said to exhibit piloerection.
ニードルパンチングしたベルトのitは用途により異な
るが150〜3009 /n?であるのか作業性の而て
准もttfましく、外見の密度は0.18097C−以
上、少なくとも0.1509/r−以−Lであるのがよ
い。The IT value of a needle-punched belt varies depending on the application, but it is 150 to 3009/n? In terms of workability, it is also desirable that the external density be 0.18097 C- or higher, or at least 0.1509/r-L or higher.
本発明において水溶性高分子の付与量は処理液の種類、
用途及び不織布の状態などにより異なるが、均一な立毛
状態、柔軟性を得るためには不織布全体の糊付量と表面
糊付量の合羽か10〜40重1%であるのがもつとも好
ましい。(第3図参6q )水溶性高分子の付与量が、
この範囲より少ない場合は効果的なバインダー(bin
der ) 効果が生じず、一方多い場合は、加圧−
Lの問題点が伴う。In the present invention, the amount of water-soluble polymer applied depends on the type of treatment liquid,
Although it varies depending on the use and the condition of the nonwoven fabric, in order to obtain a uniform raised state and flexibility, it is preferable that the amount of glue on the entire nonwoven fabric and the amount on the surface of the nonwoven fabric is 10 to 40% by weight. (See Figure 3 6q) The amount of water-soluble polymer applied is
If less than this range, an effective binder (bin
der) If no effect occurs and there is a large amount, pressurize -
This comes with the problem of L.
また、2段目の水溶性品分子の浸透の深さは前記したよ
うに糊(1された布の状態によって異flるか、基布の
厚さに対して1/12〜l / 21J、下、特に1/
12〜1/4以下とするのが最も好ましい。In addition, the penetration depth of the water-soluble product molecules in the second stage may vary depending on the state of the glue (1/1/21J to 1/21J, based on the thickness of the base fabric) as described above. Below, especially 1/
Most preferably, it is 12 to 1/4 or less.
このようにするためには処理液の濃度、特に粘度を厳し
く調節する必要があるが、大体常温、円筒型粘度計で1
00 P以上のものを使う方がよい。In order to achieve this, it is necessary to strictly control the concentration, especially the viscosity, of the processing liquid, but it is generally
It is better to use one with 00 P or more.
粘度が低すぎると処理液が基布内部に不必要に浸透し、
−万あまり高いと表面に完全なフィルム状として塗布さ
れるなど問題点が生じる。このようにして糊付された不
織布に公知のポリウレタン含と)加工を行ない、ついで
水中にて凝固及び水洗し、昇温しで前記のように処理さ
れた水溶性高分子物を完全に除去する。ポリビニルアル
コールのような水溶性高分子は大体80℃以上の熱湯で
30分以上処理すると完全に脱糊されるが、もし糊剤か
完全に除去されなければ、皮革上シート物が硬くなる恐
れがあるのセ留意しなければならない。If the viscosity is too low, the treatment liquid will unnecessarily penetrate into the fabric.
-If it is too high, problems will arise such as it being coated on the surface as a complete film. The nonwoven fabric pasted in this manner is subjected to a known process (including polyurethane), then coagulated in water, washed, and heated to completely remove the water-soluble polymer treated as described above. . Water-soluble polymers such as polyvinyl alcohol can be completely desized by treatment with boiling water of 80℃ or higher for 30 minutes or more, but if the sizing agent is not completely removed, the leather sheet may become hard. There are some things you must keep in mind.
また、前記繊維の極細化は上述のポリウレタン含浸工程
前、または後に繊維東束体に対する溶媒中でθ漬及びパ
ディング(padding )することにより容易に達
成することができ、こうして製造した皮革上シート物を
サンドペーパーが付いたサンダーでバフィングして表面
加工を行なう。In addition, the ultra-fine fibers can be easily achieved by subjecting the fiber bundle to θ-dipping and padding in a solvent before or after the polyurethane impregnation process, and the leather top sheet produced in this way can be Surface treatment is done by buffing with a sander equipped with sandpaper.
かかる表面加工は大体150メツンユのサンドペーパー
で1次バフィングして染色した後、再ひバフィングして
表面毛羽を整頓すれば、ライティング効果に優れたスェ
ード調人工皮革が得られる。This surface treatment is performed by first buffing with approximately 150 mt sandpaper, dyeing, and then re-buffing to smooth out the surface fuzz, thereby obtaining suede-like artificial leather with excellent lighting effects.
発明の効果
こうして得られた本発明の人工皮革は第5図及び第6図
に示すごとく、表面の毛羽長が−・定して、表両立毛密
度か大きくなり、繊維とポリウレタンの間に適当な空隙
が形成されて、結果的にライティング効果が増し、触感
が非常に柔らかくなり。Effects of the Invention As shown in FIGS. 5 and 6, the artificial leather of the present invention thus obtained has a constant fluff length on the surface, a high surface fluff density, and a suitable bond between the fiber and polyurethane. The resulting voids create an enhanced lighting effect and a very soft texture.
衣類用をはじめ内装斉j、履物用、鞄用なとその応用範
囲が非常に多様なスェード調人工皮革になった。Suede-like artificial leather has a wide range of applications, including clothing, interior decoration, footwear, and bags.
実施例
以下、本発明の方法によるスェード調人工皮革の製造方
法を実施例によりさらに詳細に説明する。EXAMPLES Hereinafter, the method for producing suede-like artificial leather according to the method of the present invention will be explained in more detail with reference to Examples.
本実施例において%はすべてit%を表わす。In this example, all percentages represent it%.
実施例1
ポリエチレンテレフタレート極細繊維をポリスチレンに
より集束体とした3 d x 51 IINのステーブ
ルファイバーをカーディングクロス−ラッピング及ヒニ
ードルパンチングして200g/〃〆 の不織布を得た
後、これにポリビニルアルコールヲ生成分とする水溶液
を繊維に対して固型分換算で15外付与して、ついで再
度PVA水溶液、または分散液を基布の厚さの方向に1
74以内の表面層に付与する。この時、溶液の粘度は1
10Pてあり、ナイフコーター(Knife coa
tcr )、グラビアコーター(gravure co
atcr ) などを使用する。次にテンター(tc
nter ) で乾燥し公知の侵漬法によってポリウ
レタン弾性体を充填した。これに前後してトルエンで繊
維を極細化してサンドペーパーでバフィングした。この
後、染[Qして再びパフインクして表向の毛羽を整Kf
iしたう
比較例1
比較のため水溶性品分Pを2段に付与せす、すなわち表
面部にポリビニルアルコールを付与しなかったほかは実
施例1と同じ方法で処理し人工皮革を得た。この物性を
表11ζ示す。Example 1 Stable fibers of 3 d x 51 IIN in which polyethylene terephthalate ultrafine fibers were bundled with polystyrene were carded cloth wrapped and needle punched to obtain a nonwoven fabric weighing 200 g/〃〆. Apply 15% of the aqueous solution containing the product component to the fibers in terms of solid content, and then apply 1% of the PVA aqueous solution or dispersion again in the direction of the thickness of the base fabric.
Apply to the surface layer within 74. At this time, the viscosity of the solution is 1
There are 10 pages and a knife coater.
tcr), gravure coater (gravure co
atcr) etc. Next, tenter (tc
ter) and filled with a polyurethane elastomer by a known dipping method. Before and after this, the fibers were made ultrafine with toluene and buffed with sandpaper. After this, dye [Q] and use puff ink again to smooth out the fluff on the surface.
Comparative Example 1 For comparison, artificial leather was obtained by processing in the same manner as in Example 1, except that water-soluble component P was applied in two stages, that is, polyvinyl alcohol was not applied to the surface area. The physical properties are shown in Table 11ζ.
実施例2
ポリエチレンテレフタレート極細繊維をナイロンにより
極細繊維集束体とした4 d X 64 mmのステー
プルファイバーをランダムーラツパーインク、二一ドル
ーパンチイングして25097m”の不織布を得て、こ
れにIIV八及びCMC水溶液で糊付し、再度塗布可能
な粘度を11“るPVA及びCMC水溶液を用い基布の
17さ方向に1/4 PJ、内の表面層に付写した。第
1段、第2段全体の糊付量は繊維に対して30%とした
。ついてポリウレタンを充填し、集束体の溶媒中に浸漬
、及びパディングを繰り返してナイロンを99%以上除
去した。この時、溶媒としてはギ酸、塩酸又はメタノー
ル/塩化カルシウムなどを用いることが可能であるがも
つとも溶解性が良好な水溶液にして使用した。以後、脱
糊してサンドペーパーでバフィングした。次に、分散染
料でサーキュラ−(circular )染色器を使っ
て染色し、再ひバフィングして表面ライティング効果の
非常に優れたスェード組人工皮革を得た。Example 2 A 4 d x 64 mm staple fiber in which polyethylene terephthalate ultrafine fibers were made into an ultrafine fiber bundle using nylon was punched with random wrapper ink to obtain a 25,097 m long nonwoven fabric. Then, using a PVA and CMC aqueous solution having a viscosity of 11" so that it can be reapplied, it was applied to the surface layer within 1/4 PJ in the 17th direction of the base fabric. The amount of glue applied in the first and second stages was 30% based on the fiber. The bundle was then filled with polyurethane, and 99% or more of the nylon was removed by repeatedly dipping the bundle in a solvent and padding. At this time, as a solvent, formic acid, hydrochloric acid, methanol/calcium chloride, etc. can be used, but an aqueous solution with good solubility is used. After that, I removed the glue and buffed it with sandpaper. Next, it was dyed with a disperse dye using a circular dyer, and then buffed again to obtain suede-laced artificial leather with an excellent surface lighting effect.
実施例3
実施例1で用いた不織布に20%ポリビニルアルコール
水溶液を糊付し、ついで再ひ適当な粘度のポリビニルア
ルコール水溶液を噴射法によって不織布の主に表面部に
塗布して乾燥した後、表面温度150℃の熱固定器で圧
着して表面を平滑にした。得られた不織布を実施例1と
同様の方法で加工した。Example 3 A 20% polyvinyl alcohol aqueous solution was applied to the nonwoven fabric used in Example 1, and then a polyvinyl alcohol aqueous solution of an appropriate viscosity was applied to mainly the surface of the nonwoven fabric by a spraying method, dried, and then the surface was glued. The surface was smoothed by pressure bonding using a heat fixer at a temperature of 150°C. The obtained nonwoven fabric was processed in the same manner as in Example 1.
ネ 剛軟度はカンテイレバー法によるものである。The bending resistance is determined by the cantilever method.
** ライティング効果は皮革技術者5人による官能試
験の結果で、数値が大きければ大きいほど優れている。** The lighting effect is the result of a sensory test conducted by five leather engineers, and the higher the value, the better.
上述のごとく、本発明方法によって製造さhたスェード
調人工皮革の物性値は、第1表より曳」らかなどと(剛
軟度やライティング効果など表面効果に非常に優れてい
る。As mentioned above, the physical properties of the suede-like artificial leather produced by the method of the present invention are as shown in Table 1.
第1図は第1段の糊付をねなった不織布の模式図、第2
図は第2段の糊付を行なった不織布の模式図、第3図は
糊付量に対するバフィング(buffing)性及び皮
革引張強度の関係を示すグラフ、第4図は繊維強度とバ
フィング性との関係を示すグラフ、第5図は本発明によ
って製造された製品表面の電子顕微鏡による図面代用写
真、第6図は本発明によって製造された製品側面の電子
顕微鏡による図面代用写真。Figure 1 is a schematic diagram of the nonwoven fabric with glue applied in the first stage, and the second stage
The figure is a schematic diagram of a nonwoven fabric that has undergone the second stage of sizing, Figure 3 is a graph showing the relationship between the amount of sizing applied, buffing properties and leather tensile strength, and Figure 4 is a graph showing the relationship between fiber strength and buffing properties. Graph showing the relationship; FIG. 5 is an electron microscope photograph of the surface of a product manufactured according to the present invention, and FIG. 6 is an electron microscope photograph of the side surface of a product manufactured according to the present invention.
Claims (1)
なる不織布を水溶性高分子を糊剤として第1段の糊付処
理を行ない基布とした後、再度水溶性高分子水溶液、又
は分散液を該基布の表面部に集中的に付与して第2段の
糊付処理を行ない、さらにポリウレタン弾性体を充填し
た後、前記水溶性高分子を除去しバフィングすることを
特徴とする表面効果に優れたスエード調人工皮革の製造
方法。 2、繊維がポリエステル、又はポリアミドからなる前記
第1項の方法。 3、極細化された繊維の繊度が0.001〜0.5デニ
ールである前記第1項又は第2項の方法。 4、糊剤がポリビニルアルコール、カルボキシメチルセ
ルロース、でんぷん、でんぷん類加工品、又はポリアク
リル酸、又はこれらの混合物である前記第1項の方法。 5、糊剤をパディング、コーティング、又は噴射法によ
り糊付する前記第1項、又は第4項の方法。 6、第2段の糊付量が基布の厚さ方向において基布の厚
さの1/12〜1/4の範囲である前記第1項の方法。 7、第1段および第2段の糊付量が各々繊維に対して固
型分換算で5〜20重量%である前記第1項の方法。[Claims] 1. A nonwoven fabric made of fibers with a fineness of 5 denier or less that can be made into ultra-fine fibers is subjected to a first sizing treatment using a water-soluble polymer as a sizing agent to form a base fabric, and then made into a water-soluble fabric again. A second sizing treatment is performed by intensively applying an aqueous polymer solution or dispersion to the surface of the base fabric, and after filling with a polyurethane elastomer, the water-soluble polymer is removed and buffing is performed. A method for producing suede-like artificial leather with excellent surface effects. 2. The method of item 1 above, wherein the fiber is made of polyester or polyamide. 3. The method according to item 1 or 2 above, wherein the fineness of the ultrafine fiber is 0.001 to 0.5 denier. 4. The method according to item 1 above, wherein the sizing agent is polyvinyl alcohol, carboxymethylcellulose, starch, a processed starch product, polyacrylic acid, or a mixture thereof. 5. The method of item 1 or 4 above, in which the adhesive is applied by padding, coating, or spraying. 6. The method according to item 1 above, wherein the amount of glue applied in the second stage is in the range of 1/12 to 1/4 of the thickness of the base fabric in the thickness direction of the base fabric. 7. The method according to item 1 above, wherein the amount of sizing in the first stage and the second stage is 5 to 20% by weight in terms of solid content based on the fiber.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1019840002817A KR850008196A (en) | 1984-05-23 | 1984-05-23 | Manufacturing method of suede artificial leather with excellent surface effect |
| KR84-2817 | 1984-05-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS616376A true JPS616376A (en) | 1986-01-13 |
Family
ID=19233940
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60072487A Pending JPS616376A (en) | 1984-05-23 | 1985-04-04 | Production of suede like artificial leather |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JPS616376A (en) |
| KR (1) | KR850008196A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002030577A (en) * | 2000-05-10 | 2002-01-31 | Toray Ind Inc | Method for producing leathery sheet-like product |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4832302A (en) * | 1971-08-31 | 1973-04-28 | ||
| JPS4980203A (en) * | 1972-12-04 | 1974-08-02 |
-
1984
- 1984-05-23 KR KR1019840002817A patent/KR850008196A/en not_active Ceased
-
1985
- 1985-04-04 JP JP60072487A patent/JPS616376A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4832302A (en) * | 1971-08-31 | 1973-04-28 | ||
| JPS4980203A (en) * | 1972-12-04 | 1974-08-02 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002030577A (en) * | 2000-05-10 | 2002-01-31 | Toray Ind Inc | Method for producing leathery sheet-like product |
Also Published As
| Publication number | Publication date |
|---|---|
| KR850008196A (en) | 1985-12-13 |
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