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JPH086259B2 - Synthetic leather manufacturing method - Google Patents
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JPH086259B2 - Synthetic leather manufacturing method - Google Patents

Synthetic leather manufacturing method

Info

Publication number
JPH086259B2
JPH086259B2 JP62080804A JP8080487A JPH086259B2 JP H086259 B2 JPH086259 B2 JP H086259B2 JP 62080804 A JP62080804 A JP 62080804A JP 8080487 A JP8080487 A JP 8080487A JP H086259 B2 JPH086259 B2 JP H086259B2
Authority
JP
Japan
Prior art keywords
resin
synthetic leather
layer
foam layer
raised
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 - Lifetime
Application number
JP62080804A
Other languages
Japanese (ja)
Other versions
JPS63249785A (en
Inventor
弘幸 佐藤
淳次 時枝
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bando Chemical Industries Ltd
Original Assignee
Bando Chemical Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bando Chemical Industries Ltd filed Critical Bando Chemical Industries Ltd
Priority to JP62080804A priority Critical patent/JPH086259B2/en
Publication of JPS63249785A publication Critical patent/JPS63249785A/en
Publication of JPH086259B2 publication Critical patent/JPH086259B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, 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
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/12Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
    • D06N3/14Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyurethanes
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, 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
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/007Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by mechanical or physical treatments
    • D06N3/0079Suction, vacuum treatment

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Laminated Bodies (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明は合成皮革の製造方法に関し、詳しくは、機械
発泡層を含みながら、層間強度にすぐれ、且つ、軽量で
柔軟な合成皮革、及びかかる合成皮革の製造方法に関す
る。
Description: TECHNICAL FIELD The present invention relates to a method for producing synthetic leather, and more specifically, to a synthetic leather which has a mechanical foaming layer, has excellent interlayer strength, and is lightweight and flexible, and such synthetic leather. Manufacturing method.

従来の技術 従来、合成皮革の代表的な製造方法として、機械発泡
法が知られている。この機械発泡法とは、ポリウレタン
等の樹脂溶液を機械的に撹拌し、溶液内に微小な空気泡
を形成させ、このように機械発泡させた樹脂溶液をメリ
ヤス、織布等の起毛を有しない基布の上に塗布した後、
樹脂を硬化させ、次いで、この上に例えばウレタン樹脂
にて表皮層を接着させて、合成皮革を製造するものであ
る。
2. Description of the Related Art Conventionally, a mechanical foaming method has been known as a typical method for producing synthetic leather. In this mechanical foaming method, a resin solution such as polyurethane is mechanically stirred to form minute air bubbles in the solution, and the mechanically foamed resin solution does not have knitted fabric, woven fabric, or the like. After applying on the base cloth,
The resin is cured, and then a skin layer is adhered onto the resin with, for example, a urethane resin to produce synthetic leather.

かかる方法にて得られる合成皮革は、非常に軽量で柔
軟ではあるが、しかし、発泡層は、何らの補強手段を含
まないので、その凝集破壊強度は僅かに0.8〜1.0kg/cm
程度にすぎず、層間強度が著しく小さいために、合成皮
革がこの発泡層において容易に破断し、従つて、例え
ば、スポーツシユーズの胛被等に用いることが困難であ
る。更に、合成皮革を折り曲げたときに、発泡層に柔ら
かすぎるために、表皮層に大きい折りしわが生じやす
い。
The synthetic leather obtained by such a method is very lightweight and flexible, but since the foam layer does not include any reinforcing means, its cohesive failure strength is only 0.8 to 1.0 kg / cm.
However, since the interlayer strength is extremely small, the synthetic leather easily breaks in this foamed layer, and thus it is difficult to use it, for example, as a cover for sports shoes. Further, when the synthetic leather is bent, the foam layer is too soft, so that large creases are likely to occur in the skin layer.

発明が解決しようとする問題点 そこで、本発明者らは、機械発泡層を含む従来の合成
皮革における上記した問題を解決するために鋭意研究し
た結果、基布として起毛布を用い、これに機械発泡させ
た樹脂溶液を強制的に含浸させ、硬化させて、起毛を含
む発泡層を形成し、このようにして、機械発泡層を起毛
にて補強することによつて、軽量で柔軟な性質を保持さ
せたまま、層間強度を高めた合成皮革を得ることができ
ることを見出して、本発明に至つたものである。
Problems to be Solved by the Invention Therefore, as a result of intensive studies to solve the above-mentioned problems in the conventional synthetic leather including a mechanical foam layer, the present inventors have used a raised fabric as a base fabric, and The foamed resin solution is forcibly impregnated and cured to form a foamed layer containing naps, and in this way, the mechanical foamed layer is reinforced with naps to provide a lightweight and flexible property. The inventors of the present invention have found that it is possible to obtain a synthetic leather having an increased interlaminar strength while it is held.

問題点を解決するための手段 本発明による合成皮革の製造方法は、基布の上に樹脂
発泡層及び表皮層が形成されている合成皮革の製造方法
において、起毛布上に機械発泡させた樹脂配合物を塗布
した後、上記起毛布の下から吸引し、上記樹脂配合物を
起毛布に強制的に含浸させた後、樹脂を硬化させて、樹
脂発泡層を形成することを特徴とする。
Means for Solving Problems A synthetic leather production method according to the present invention is a synthetic leather production method in which a resin foam layer and a skin layer are formed on a base cloth, and a resin mechanically foamed on a raised cloth is used. The composition is characterized in that after the composition is applied, suction is applied from under the raised fabric to forcefully impregnate the raised fabric with the resin composition, and then the resin is cured to form a resin foam layer.

本発明において基布として用いる起毛布は、好ましく
は長さ400〜1100μmの長さの起毛を有し、本発明によ
れば、起毛布の原撚糸層まで起毛を含んで、機械発泡層
を形成させる。一般に、起毛布上に機械発泡させた樹脂
溶液を塗布しても、樹脂溶液は、起毛層の上に層を形成
するのみであつて、起毛を含むように、起毛布に含浸さ
せることができない。しかし、本発明に従つて、起毛布
に機械発泡させた樹脂溶液を塗布した後、起毛されてい
ない面、即ち、裏面から吸引することによつて、樹脂溶
液を起毛布の原撚糸層まで含浸させることができる。こ
のようにして、機械発泡させた樹脂溶液を起毛を含む起
毛布に含浸させた後、樹脂を硬化させることによつて、
起毛布の原撚糸層まで起毛を含む機械発泡層を形成させ
ることができる。
The napped cloth used as the base cloth in the present invention preferably has naps with a length of 400 to 1100 μm, and according to the present invention, the nap is formed up to the original twisted yarn layer of the napped cloth to form a mechanical foam layer. Let In general, when a mechanically foamed resin solution is applied onto a napped cloth, the resin solution only forms a layer on the napped layer and cannot be impregnated into the napped cloth so as to include the nap. . However, according to the present invention, after the mechanically foamed resin solution is applied to the napped cloth, the resin solution is impregnated to the original twisted yarn layer of the napped cloth by sucking from the non-raised surface, that is, the back surface. Can be made. In this way, by impregnating the raised fabric containing the raised fabric with the mechanically foamed resin solution, and then curing the resin,
It is possible to form a mechanically foamed layer including raised fibers up to the original twisted yarn layer of the raised fabric.

この後、発泡層をバフイング等の適宜手段によつて表
面を平滑にし、この上に接着剤を介して、表皮層を接着
すれば、本発明による合成皮革を得ることができる。
After that, the surface of the foamed layer is smoothed by an appropriate means such as buffing, and the skin layer is adhered onto the foamed layer via an adhesive to obtain the synthetic leather of the present invention.

第1図は、このようにして得られる本発明による合成
皮革の断面図を示し、起毛1を有する起毛布2を基布と
して、その原撚糸層3まで起毛を含む機械発泡層4が形
成され、この発泡層が接着剤層5を介して、表皮層6に
接着されている。特に、限定されるものではないが、こ
のようにして形成される合成皮革においては、起毛布の
原撚糸層の厚さが400μm程度、機械発泡層の厚さが700
μm程度、接着剤層の厚さ及び表皮層の厚さがいずれも
20〜30μm程度であるのが好適である。
FIG. 1 shows a cross-sectional view of the synthetic leather according to the present invention obtained in this manner, in which a raised fabric 2 having raised fabric 1 is used as a base fabric to form a mechanical foam layer 4 including raised fabrics up to the original twisted yarn layer 3. This foam layer is bonded to the skin layer 6 via the adhesive layer 5. Although not particularly limited, in the synthetic leather thus formed, the thickness of the original twisted yarn layer of the raised fabric is about 400 μm and the thickness of the mechanical foam layer is 700 μm.
About μm, both the adhesive layer thickness and the skin layer thickness
It is preferably about 20 to 30 μm.

本発明においては、機械発泡層を形成する樹脂として
は、特に、ウレタン樹脂又はアクリル酸エステル共重合
体が好ましく用いられるが、かかる場合において、樹脂
溶液の機械発泡倍率は、1.7〜4.5倍、特に、2〜4倍の
範囲が好ましい。発泡倍率が1.5倍よりも小さいとき
は、発泡層の機械強度は大きいが、比重が大きく、軽量
性に欠けるのみならず、発泡層が硬すぎることとなり、
他方、5.0倍よりも大きいときは、非常に軽量ではある
が、基布として従来のメリヤス等を用いる場合に比べ
て、形成される発泡層の層間強度が殆ど向上しないから
である。
In the present invention, as the resin forming the mechanical foam layer, a urethane resin or an acrylate copolymer is particularly preferably used, but in such a case, the mechanical expansion ratio of the resin solution is 1.7 to 4.5 times, particularly, The range of 2 to 4 times is preferable. When the expansion ratio is less than 1.5 times, the mechanical strength of the foam layer is large, but the specific gravity is large, not only lacking in lightness, but also the foam layer is too hard,
On the other hand, when it is more than 5.0 times, it is very lightweight, but the interlayer strength of the foamed layer formed is hardly improved as compared with the case of using a conventional knitted fabric or the like as the base fabric.

発明の効果 以上のように、本発明による合成皮革によれば、起毛
布を基布とし、その起毛を含むように機械発泡層が形成
されているので、発泡層は起毛の補強硬化によつて、通
常、1.5kg/cm以上の層間強度を有し、しかも、機械発泡
層による軽量性及び柔軟性を保持している。
Effects of the Invention As described above, according to the synthetic leather of the present invention, the napped fabric is used as the base fabric, and the mechanical foam layer is formed so as to include the nap. Therefore, the foam layer is formed by reinforcing and hardening the nap. Generally, it has an interlayer strength of 1.5 kg / cm or more, and yet retains the lightness and flexibility of the mechanical foam layer.

実施例 以下に実施例を挙げて本発明を説明するが、本発明は
これら実施例により何ら限定されるものではない。
EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited to these examples.

実施例1 下記の組成(部数は重量部を示す。) ウレタン樹脂エマルジヨン(アニオン系、保土谷化学工
業(株)製S4040N 100部 水溶性メラミン樹脂(保土谷化学工業(株)製O)8部 水溶性メラミン樹脂(保土谷化学工業(株)製P)6部 整泡剤(保土谷化学工業(株)製DF18) 6部 増粘剤(保土谷化学工業(株)製LV30) 2部 からなる配合物をその発泡倍率が4倍になるまで電動泡
立機にて機械的に撹拌した。
Example 1 The following composition (parts indicate parts by weight): Urethane resin emulsion (anion type, S4040N manufactured by Hodogaya Chemical Co., Ltd. 100 parts) Water-soluble melamine resin (O manufactured by Hodogaya Chemical Co., Ltd.) 8 parts Water-soluble melamine resin (P from Hodogaya Chemical Co., Ltd.) 6 parts Foam stabilizer (DF18 from Hodogaya Chemical Co., Ltd.) 6 parts Thickener (LV30 from Hodogaya Chemical Co., Ltd.) 2 parts The resulting mixture was mechanically stirred with an electric whisk until the foaming ratio became 4 times.

この機械発泡させた樹脂配合物をナイフコーターにて
起毛布上に塗布し、裏面側から吸引して、配合物を起毛
布に強制的に含浸させた後、80℃の温度に2分間加熱乾
燥し、更に、135℃の温度に2分間加熱して、樹脂を架
橋硬化させて、樹脂発泡層を形成させた。この後、この
発泡層の表面をバフイングして平滑にした。
This mechanically foamed resin mixture is applied to a napped cloth with a knife coater, suctioned from the back side to forcibly impregnate the napped cloth with the mixture, and then dried by heating at a temperature of 80 ° C for 2 minutes. Then, the resin was further heated at a temperature of 135 ° C. for 2 minutes to crosslink and cure the resin to form a resin foam layer. Then, the surface of this foam layer was buffed to be smooth.

別に、適当に着色したウレタン樹脂(大日本インキ化
学工業(株)製レザミン2825LP)を10μm厚みに離型紙
上にリバースコーターにて塗布し、100℃の温度で2分
間加熱乾燥させた後、その上にウレタン樹脂接着剤(大
日本インキ化学工業(株)製クリスボン4090)を20μm
厚みに塗布し、120℃で1分間加熱した。
Separately, an appropriately colored urethane resin (Resamine 2825LP manufactured by Dainippon Ink and Chemicals, Inc.) was applied on a release paper to a thickness of 10 μm by a reverse coater and dried by heating at 100 ° C. for 2 minutes. 20 μm of urethane resin adhesive (Crisbon 4090 manufactured by Dainippon Ink and Chemicals, Inc.) on top
It was applied to a thickness and heated at 120 ° C for 1 minute.

この離型紙の接着剤塗布面を上記バフイングした発泡
層に重ねて加圧し、冷却した後、離型紙を剥離して、合
成皮革を得た。
The adhesive-coated surface of this release paper was superposed on the buffed foamed layer, pressed and cooled, and then the release paper was peeled off to obtain a synthetic leather.

このようにして得た合成皮革は、セル径10〜30μm、
セル数密度100000〜150000個/cm2、比重0.30〜0.32g/cm
3、剛軟度(カンチレバー)7.0cm、JIS A硬度55度であ
つて、軽量柔軟であり、しかも、樹脂発泡層の層間強度
は1.5〜1.7kg/cmであつて、従来の合成皮革における機
械発泡層の層間強度に比べて、著しく改善されている。
The synthetic leather thus obtained has a cell diameter of 10 to 30 μm,
Cell number density 100000 to 150,000 cells / cm 2 , specific gravity 0.30 to 0.32 g / cm
3. Bending flexibility (cantilever) 7.0 cm, JIS A hardness 55 degrees, light weight and flexibility, and resin foam layer interlayer strength of 1.5 to 1.7 kg / cm. Compared with the interlayer strength of the foam layer, it is significantly improved.

実施例2 下記の組成(部数は重量部を示す。) アクリル酸エステル共重合体(大日本インキ化学工業
(株)製ボンコートAF615) 100部 メラミン樹脂(保土谷化学工業(株)製) 5部 架橋剤(大日本インキ化学工業(株)製パーマスタツト
CR5) 2部 28%アンモニア水 1部 からなる配合物をその発泡倍率が4倍になるまで電動泡
立機にて機械的に撹拌した。
Example 2 The following composition (parts indicate parts by weight): Acrylic ester copolymer (Bonn Coat AF615 manufactured by Dainippon Ink and Chemicals, Inc.) 100 parts Melamine resin (manufactured by Hodogaya Chemical Co., Ltd.) 5 parts Cross-linking agent (Permastat manufactured by Dainippon Ink and Chemicals, Inc.)
CR5) A mixture consisting of 2 parts and 1 part of 28% ammonia water was mechanically stirred by an electric whisk until the expansion ratio became 4 times.

この機械発泡させた発泡樹脂配合物をナイフコーター
にて起毛布上に塗布し、裏面側から吸引して、配合物を
起毛布に強制的に含浸させた後、100℃の温度で5分間
加熱乾燥し、更に、140℃の温度に5分間加熱して、樹
脂を架橋硬化させて、樹脂発泡層を形成させた。この
後、この発泡層の表面をバフイングして平滑にした。
The foamed resin composition mechanically foamed is applied onto a napped cloth with a knife coater, sucked from the back side to forcefully impregnate the napped cloth with the composition, and then heated at a temperature of 100 ° C. for 5 minutes. The resin was dried and further heated at a temperature of 140 ° C. for 5 minutes to crosslink and cure the resin to form a resin foam layer. Then, the surface of this foam layer was buffed to be smooth.

別に、適当に着色したウレタン樹脂(大日本インキ化
学工業(株)製レザミン2825LP)を10μm厚みに離型紙
上にリバースコーターにて塗布し、100℃の温度で2分
間加熱乾燥させた後、その上にウレタン樹脂接着剤(大
日本インキ化学工業(株)製クリスボン4090)を20μm
厚みに塗布し、120℃で1分間加熱した。
Separately, an appropriately colored urethane resin (Resamine 2825LP manufactured by Dainippon Ink and Chemicals, Inc.) was applied on a release paper with a thickness of 10 μm by a reverse coater, and dried by heating at 100 ° C. for 2 minutes, 20 μm of urethane resin adhesive (Crisbon 4090 manufactured by Dainippon Ink and Chemicals, Inc.) on top
It was applied to a thickness and heated at 120 ° C for 1 minute.

この離型紙の接着剤塗布面を上記バフイングした発泡
層に重ねて加圧し、冷却した後、離型紙を剥離して、合
成皮革を得た。
The adhesive-coated surface of this release paper was superposed on the buffed foamed layer, pressed and cooled, and then the release paper was peeled off to obtain a synthetic leather.

このようにして得た合成皮革は、セル径5〜10μm、
セル数密度100000〜150000個/cm2、比重0.32〜0.35g/cm
3、剛軟度7.0cm、JIS A硬度50度であつて、軽量柔軟で
あり、しかも、樹脂発泡層の層間強度は1.5〜2.0kg/cm
であつて、従来の合成皮革における機械発泡層の層間強
度に比べて、著しく改善されている。
The synthetic leather thus obtained has a cell diameter of 5 to 10 μm,
Cell number density 100000 to 150,000 cells / cm 2 , specific gravity 0.32 to 0.35 g / cm
3 , lightness and flexibility of 7.0 cm, JIS A hardness of 50 degrees, light and flexible, and the interlayer strength of the resin foam layer is 1.5 to 2.0 kg / cm
However, it is remarkably improved as compared with the interlayer strength of the mechanical foam layer in the conventional synthetic leather.

比較例 実施例1におけると同じ配合物をその発泡倍率が4倍
になるまで電動泡立機にて機械的に撹拌した。
Comparative Example The same formulation as in Example 1 was mechanically agitated with an electric whisk until the expansion ratio was 4 times.

この気化発泡させた樹脂配合物をナイフコーターにて
メリヤス基布の上に塗布し、80℃の温度で2分間加熱乾
燥し、更に、135℃の温度に2分間加熱して、樹脂を架
橋硬化させて、樹脂発泡層を形成させた。この後、この
発泡層の表面をバフイングして平滑にした。
This vaporized and foamed resin composition is applied on a knitted fabric with a knife coater, heated and dried at a temperature of 80 ° C for 2 minutes, and further heated at a temperature of 135 ° C for 2 minutes to crosslink and cure the resin. Then, the resin foam layer was formed. Then, the surface of this foam layer was buffed to be smooth.

別に、適当に着色したウレタン樹脂(大日本インキ化
学工業(株)製レザミン2825LP)を10μm厚みに離型紙
上にリバースコーターにて塗布し、100℃の温度で2分
間加熱乾燥させた後、その上にウレタン樹脂接着剤(大
日本インキ化学工業(株)製クリスボン4090)を20μm
厚みに塗布し、120℃で1分間加熱した。
Separately, a properly colored urethane resin (Resamine 2825LP manufactured by Dainippon Ink and Chemicals, Inc.) was applied on a release paper with a thickness of 10 μm by a reverse coater, and dried by heating at 100 ° C. for 2 minutes. 20 μm of urethane resin adhesive (Crisbon 4090 manufactured by Dainippon Ink and Chemicals, Inc.) on top
It was applied to a thickness and heated at 120 ° C for 1 minute.

この離型紙を接着剤塗布面を上記バフイングした発泡
層に重ねて加圧し、冷却した後、離型紙を剥離して、合
成皮革を得た。
The release paper was superposed on the buffing foamed layer with the adhesive-coated surface, pressed and cooled, and then the release paper was peeled off to obtain a synthetic leather.

このようにして得た合成皮革は、セル径10〜30μm、
セル数密度100000〜150000個/cm2、比重0.25〜0.27g/cm
3、剛軟度7.0cm、JIS A硬度45度であつて、軽量柔軟で
あつたが、樹脂発泡層の層間強度は僅かに0.8〜1.0kg/c
mであつた。
The synthetic leather thus obtained has a cell diameter of 10 to 30 μm,
Cell number density 100000 to 150,000 cells / cm 2 , specific gravity 0.25 to 0.27 g / cm
3 , lightness and flexibility of 7.0 cm and JIS A hardness of 45 degrees, but the interlayer strength of the resin foam layer was only 0.8 to 1.0 kg / c.
It was m.

実施例3 実施例1におけると同じ樹脂配合物を用い、発泡倍率
を変えた以外は、実施例1と同様にして、合成皮革を製
造した。これらの性質を第1表に示す。
Example 3 A synthetic leather was produced in the same manner as in Example 1 except that the same resin composition as in Example 1 was used and the expansion ratio was changed. These properties are shown in Table 1.

発泡倍率を1.5倍としたときは、得られる合成皮革の
比重が大きすぎて、軽量性に欠けると共に、発泡層が硬
すぎる。他方、発泡倍率を5.0倍としたときは、非常に
軽量ではあるが、発泡層の層間強度が小さすぎる。
When the expansion ratio is set to 1.5 times, the resulting synthetic leather has too large a specific gravity, is not lightweight, and the foam layer is too hard. On the other hand, when the expansion ratio is 5.0, it is very lightweight, but the interlayer strength of the foam layer is too small.

【図面の簡単な説明】[Brief description of drawings]

第1図は、本発明による合成皮革の断面図を示す。 1……起毛、2……起毛布、3……原撚糸層、4……機
械発泡層、5……接着剤層、6……表皮層。
FIG. 1 shows a sectional view of a synthetic leather according to the present invention. 1 ... Brushed, 2 ... Raised cloth, 3 ... Original twisted yarn layer, 4 ... Mechanical foam layer, 5 ... Adhesive layer, 6 ... Skin layer.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】基布の上に樹脂発泡層及び表皮層が形成さ
れている合成皮革の製造方法において、起毛布上に機械
発泡させた樹脂配合物を塗布した後、上記起毛布の下か
ら吸引し、上記樹脂配合物を起毛布に強制的に含浸させ
た後、樹脂を硬化させて、樹脂発泡層を形成することを
特徴とする合成皮革の製造方法。
1. A method for producing synthetic leather in which a resin foam layer and a skin layer are formed on a base cloth, after applying a mechanically foamed resin composition onto a raised cloth, and then from below the raised cloth. A method for producing synthetic leather, which comprises sucking and forcibly impregnating a raised fabric with the above-mentioned resin composition, and then curing the resin to form a resin foam layer.
JP62080804A 1987-03-31 1987-03-31 Synthetic leather manufacturing method Expired - Lifetime JPH086259B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62080804A JPH086259B2 (en) 1987-03-31 1987-03-31 Synthetic leather manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62080804A JPH086259B2 (en) 1987-03-31 1987-03-31 Synthetic leather manufacturing method

Publications (2)

Publication Number Publication Date
JPS63249785A JPS63249785A (en) 1988-10-17
JPH086259B2 true JPH086259B2 (en) 1996-01-24

Family

ID=13728651

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62080804A Expired - Lifetime JPH086259B2 (en) 1987-03-31 1987-03-31 Synthetic leather manufacturing method

Country Status (1)

Country Link
JP (1) JPH086259B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003003379A (en) * 2001-06-21 2003-01-08 Koatsu Cloth Kk Sheet structural body and method for producing the same
WO2013056401A1 (en) * 2011-10-21 2013-04-25 Bayer Materialscience Ag Process for the production of coated textiles
WO2014097999A1 (en) * 2012-12-18 2014-06-26 共和レザー株式会社 Laminated sheet and method of manufacturing same
JP2018150649A (en) * 2017-03-14 2018-09-27 株式会社クラレ Silver-like artificial leather and method for producing the same
JPWO2025109904A1 (en) * 2023-11-20 2025-05-30

Also Published As

Publication number Publication date
JPS63249785A (en) 1988-10-17

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