JPH0320116Y2 - - Google Patents
Info
- Publication number
- JPH0320116Y2 JPH0320116Y2 JP12685485U JP12685485U JPH0320116Y2 JP H0320116 Y2 JPH0320116 Y2 JP H0320116Y2 JP 12685485 U JP12685485 U JP 12685485U JP 12685485 U JP12685485 U JP 12685485U JP H0320116 Y2 JPH0320116 Y2 JP H0320116Y2
- Authority
- JP
- Japan
- Prior art keywords
- cloth
- vinyl chloride
- foam layer
- chloride resin
- layer
- 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
- 239000006260 foam Substances 0.000 claims description 32
- 239000004744 fabric Substances 0.000 claims description 31
- 239000000835 fiber Substances 0.000 claims description 17
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 12
- 229920005989 resin Polymers 0.000 claims description 12
- 239000011347 resin Substances 0.000 claims description 12
- 229920001971 elastomer Polymers 0.000 claims description 11
- 239000000806 elastomer Substances 0.000 claims description 9
- 238000005187 foaming Methods 0.000 claims description 7
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 6
- 239000004800 polyvinyl chloride Substances 0.000 claims description 6
- 239000004014 plasticizer Substances 0.000 claims description 5
- 229920001084 poly(chloroprene) Polymers 0.000 claims description 4
- 229920000459 Nitrile rubber Polymers 0.000 claims 3
- 239000004709 Chlorinated polyethylene Substances 0.000 claims 2
- 229920001577 copolymer Polymers 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 239000000853 adhesive Substances 0.000 description 18
- 230000001070 adhesive effect Effects 0.000 description 18
- 230000035699 permeability Effects 0.000 description 8
- 229920003002 synthetic resin Polymers 0.000 description 7
- 239000000057 synthetic resin Substances 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000010985 leather Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000004156 Azodicarbonamide Substances 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 2
- 235000019399 azodicarbonamide Nutrition 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- -1 drying quickly Substances 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Description
【考案の詳細な説明】
イ 考案の目的
(産業上の利用分野)
この考案は合成樹脂製レザーに係るものであり
自動車用座席シート、自動車用内層材、衣料用布
地、家具用レザーなど、特に壁装材、その他室内
装飾用に広く利用されるものである。[Detailed explanation of the invention] A. Purpose of the invention (industrial application field) This invention relates to synthetic resin leather, and is particularly applicable to automobile seats, inner layer materials for automobiles, fabrics for clothing, leather for furniture, etc. It is widely used for wall coverings and other interior decoration purposes.
(従来の技術)
従来上記の用途に用いられる合成樹脂レザーの
多くは、レーヨン、綿、麻等の天然繊維、ポリエ
ステル等の合成樹脂繊維等からなる織物、編物1
と塩化ビニル樹脂発泡体2とを積層したものがし
られているが、この種の繊維は塩化ビニルとの相
溶性に欠けるため、熱融着しただけでは強固に積
層することができない、従つて積層する前に予め
接着剤を塗布した布地を使用したり、又は発泡体
層(未発泡体層を含む)表面に接着剤3を塗布
し、未乾燥の状態で布地を貼りあわせることによ
りこの接着剤をバインダーとして両者を接着した
ものが殆どである(第3図参照)。(Prior art) Most of the synthetic resin leathers conventionally used for the above-mentioned purposes are woven or knitted fabrics made of natural fibers such as rayon, cotton, and hemp, and synthetic resin fibers such as polyester.
It is known that fibers of this type are laminated with polyvinyl chloride resin foam 2, but since this type of fiber lacks compatibility with vinyl chloride, it cannot be strongly laminated just by heat-sealing. This adhesion can be achieved by using fabrics coated with adhesive in advance before lamination, or by applying adhesive 3 to the surface of the foam layer (including the unfoamed layer) and laminating the fabrics in a wet state. In most cases, the two are bonded together using a binder (see Figure 3).
しかしながらこの公知の物においては、接着剤
塗布工程を必要とし、使用される接着剤が溶剤タ
イプの場合には、その揮発ガスにより作業環境が
悪化する。また引火の恐れもあり危険であり、接
着剤として水溶性のものを用いるときは特別の乾
燥工程を必要とし、製造コストが著しく押し上げ
られる。殊にかかる接着剤を使用した場合、接着
剤が布地中に浸透し織目を固定することによつて
製品の風合を損ねるばかりでなく、また接着剤が
繊維間の空隙を埋めることによつて、透湿性を失
う。この結果壁層材にあつては結露を生じ、また
加工時に使用する糊の乾燥を遅らせるなどの欠点
を生じる。更に製品がカールすることもあり後の
裁断や縫製加工が困難となる欠点を有した。 However, this known product requires an adhesive application step, and if the adhesive used is a solvent type, the working environment will be degraded by its volatile gas. Furthermore, it is dangerous due to the risk of ignition, and when a water-soluble adhesive is used, a special drying process is required, which significantly increases manufacturing costs. Particularly when such adhesives are used, they not only impair the feel of the product by penetrating into the fabric and fixing the weave, but also impair the feel of the product by filling the voids between the fibers. It loses its moisture permeability. As a result, dew condensation occurs in the wall layer material, and the drying of the glue used during processing is delayed. Furthermore, the product sometimes curls, making subsequent cutting and sewing difficult.
また透湿性を有する塩化ビニル製の壁装材とし
ては実公昭57−13360号実用新案公報が知られて
いるが、この先行技術のものは粗布の片面に紙1
4を添え、他の面より合成樹脂を縞状に設けて、
紙と合成樹脂を融着させ、合成樹脂のない部分を
通じて透湿性を附与しているもので、全面合成樹
脂でなく、強度に劣り意匠的にも著しく制限を受
ける(第4図参照)
(考案が解決しようとする課題)
この考案のものは、前記先行技術の欠点を発泡
層の構造及び組成を変えることによつて解決し、
下引接着剤を用いず、風合に富み、外観の色彩、
凹凸模様等の意匠的表現が自由にでき、水分に対
して強く、布地表面のひつかき強度にも優れ、透
湿性のあるシート状物積層体を得ることを目的と
する。 In addition, Utility Model Publication No. 57-13360 is known as a wall covering material made of vinyl chloride that has moisture permeability, but this prior art has one layer of paper on one side of the sackcloth.
4, and put synthetic resin in stripes from the other side,
Paper and synthetic resin are fused together to provide moisture permeability through the parts without synthetic resin, and because they are not entirely made of synthetic resin, they are inferior in strength and have significant design limitations (see Figure 4). Problems to be Solved by the Invention) This invention solves the drawbacks of the prior art by changing the structure and composition of the foam layer,
No undercoat adhesive is used, giving a rich texture and exterior color.
The purpose of the present invention is to obtain a sheet-like material laminate that can freely express a design such as an uneven pattern, is strong against moisture, has excellent resistance to rubbing on the fabric surface, and has moisture permeability.
ロ 考案の構成
(課題を解決するための手段)
この考案は前記の課題を達成するために塩化ビ
ニル樹脂及び可塑剤と、これらと相溶性を有する
エラストマを配合した前記三成分を含む塩化ビニ
ル組成物からなるシート状物を発泡直後の融軟状
態の発泡層に粗目の布状物を圧接して、前記布状
物の一部の繊維糸が前記発泡層中にめり込んで発
泡層の表裏に露出した部分が平均的に分布してい
ることを特徴とする塩化ビニル樹脂発泡シート状
積層体とする。B. Structure of the invention (means for solving the problem) In order to achieve the above-mentioned problem, this invention is a vinyl chloride composition containing the above three components, which is a vinyl chloride resin, a plasticizer, and an elastomer that is compatible with these. A coarse cloth-like material is pressed against a foam layer in a melted and softened state immediately after foaming, and some of the fiber threads of the cloth-like material sink into the foam layer and form on the front and back sides of the foam layer. A polyvinyl chloride resin foam sheet-like laminate is characterized in that the exposed portions are evenly distributed.
(実施例)
今この考案を実用新案登録請求の範囲第1項乃
至第5項の記載の考案を含む実施例について説明
する。(Embodiment) Now, an embodiment of this invention including the invention described in the claims 1 to 5 of the utility model registration claims will be described.
実施例 1
第1図において10は寒冷紗、廉布などの粗目
の布であり、この表面に塩化ビニルよりなる組成
物発泡層11が接着剤などを用いることなく接着
してあり、前記発泡層11が加熱融軟状態のうち
に、前記粗目の布10を発泡層にめり込ませて、
後冷却して製品が形成されており、前記粗目の布
10の糸乃至繊維の一部はこの積層体の表裏双方
に露出して、この露出部分12は積層体の表裏前
面にそれぞれの面において平均分布している13
は凹凸模様である。Example 1 In FIG. 1, reference numeral 10 is a coarse cloth such as cheesecloth or cloth, and a foamed composition layer 11 made of vinyl chloride is adhered to the surface of this cloth without using an adhesive or the like. While it is heated and melted, the coarse cloth 10 is sunk into the foam layer,
After cooling, a product is formed, and a part of the threads or fibers of the coarse cloth 10 are exposed on both the front and back sides of the laminate, and the exposed portions 12 are formed on each of the front and back surfaces of the laminate. Average distribution 13
has an uneven pattern.
今この考案の前記塩化ビニル組成物の組成並び
に製造方法を次に説明する。 The composition and manufacturing method of the vinyl chloride composition of this invention will now be explained.
例1.
配合成分 重量部
イ 塩化ビニル樹脂
(平均重合度900)
50部
ロ エラストマ 60部
内訳 塩化ビニル−酢酸ビニル
共重合体……50部
NBR……10部
ハ 可塑剤 DOP 50部
ニ その他の添加物
炭酸カルシユウム 30部
発泡剤:アゾジカルボンアミド 3部
安定剤:Ba−Zn系 3部
上記配合物をミキサーで充分に混合し、組成物
として、厚さ0.22mmのフイルムを成形した。次に
当該フイルムを裏打紙(米秤80g/m2)14にラ
ミネートした後、フイルム面にグラビア印刷法に
よつて、所定の模様を印刷した。次にラミネート
機を用いて、前記フイルム面に粗目の布10の一
種たる寒冷紗(縦糸ポリエステル30デニール、打
込本数20本/2.54cm、緯糸麻単糸10番手、打込本
数20本/2.54cm)を重ねた状態で投入しフイルム
表面150〜160℃にて両者を圧接してラミネートし
た。次に発泡炉中で200〜210℃の温度で60秒〜90
秒間加熱して、発泡させ、発泡炉を出た直後に、
発泡層がまだ融軟状態の間に、所定の凹凸模様を
刻設したエンボスローラ及びゴムローラ間で圧着
して、寒冷紗を重合した発泡層11の表面に凹凸
模様13を形成し、同時に発泡層11と寒冷紗1
0及び裏打紙14を圧接一体化する。この凹凸ロ
ーラによる圧力は線圧1tonで行つた。このように
して製造したこの考案のものは、凹凸模様の凸部
15の厚みが0.60〜0.80mm、凹部16では0.25〜
0.35mmとなり、この凹部においては粗目の布10
の一部の糸乃至繊維の一部が凹凸模様側に露出す
る。Example 1. Compounding components Parts by weight Vinyl chloride resin (average degree of polymerization 900) 50 parts Elastomer 60 parts Breakdown Vinyl chloride-vinyl acetate copolymer...50 parts NBR...10 parts C Plasticizer DOP 50 parts D Other Additives Calcium carbonate 30 parts Foaming agent: Azodicarbonamide 3 parts Stabilizer: Ba-Zn type 3 parts The above formulation was thoroughly mixed with a mixer, and the composition was molded into a film with a thickness of 0.22 mm. Next, the film was laminated onto backing paper (80 g/m 2 on a rice scale) 14, and a predetermined pattern was printed on the film surface by gravure printing. Next, using a laminating machine, cheesecloth (warp 30 denier, number of threads 20/2.54cm, weft yarn hemp single yarn count 10, number of threads 20/2.54cm) is placed on the film surface, which is a type of coarse cloth 10. ) were placed in a stacked state and the two were pressed together at a temperature of 150 to 160° C. to laminate the film surface. Then in a foaming oven at a temperature of 200-210℃ for 60 seconds-90
Heat for seconds to foam, and immediately after exiting the foaming furnace,
While the foam layer is still in a molten and soft state, it is pressed between an embossing roller and a rubber roller on which a predetermined uneven pattern has been engraved to form an uneven pattern 13 on the surface of the foam layer 11 made of polymerized cheesecloth, and at the same time, the foam layer 11 and cheesecloth 1
0 and the backing paper 14 are integrated by pressure bonding. The pressure by this uneven roller was applied at a linear pressure of 1 ton. In this device manufactured in this manner, the thickness of the convex portions 15 of the uneven pattern is 0.60 to 0.80 mm, and the thickness of the concave portions 16 is 0.25 to 0.25 mm.
0.35mm, and in this recess, coarse cloth 10
Some of the threads or fibers are exposed on the uneven pattern side.
前記発泡層11と布10との結合は単に物理的
な結合だけでなく、前記塩化ビニル組成物の接着
力と相まつて、強固に結合されている。しかし、
融軟状態でも前記組成物は接着剤(エマルジヨ
ン、溶剤タイプ)より粘度が高く、濡れ適正も小
さいことから布生地の繊維の空隙を埋めるには到
らず繊維の透湿性は保持される。 The bond between the foam layer 11 and the cloth 10 is not only a physical bond, but also a strong bond due to the adhesive force of the vinyl chloride composition. but,
Even in the melted and softened state, the composition has a higher viscosity than adhesives (emulsion, solvent type) and has a lower wettability, so it does not fill the voids in the fibers of the fabric, and the moisture permeability of the fibers is maintained.
特に前記組成物中には塩化ビニル樹脂及び可塑
剤と相溶性を有するエラストマが配合されている
ため、これらエラストマは加熱時に接着したもの
が冷却後接着強度を高めるため、更に布生地とは
強固に接着している。 In particular, since the composition contains an elastomer that is compatible with vinyl chloride resin and a plasticizer, these elastomers are bonded during heating to increase the adhesive strength after cooling, and are even more strongly bonded to fabrics. It's glued.
実施例 2
第2図においては、前記第1図の実施例と異な
り、粗目の布10の面より凹凸が施されており布
10と反対面には通気、透湿性のある裏打紙14
が貼付されている。その他は第1図のものと同一
である。Embodiment 2 In FIG. 2, unlike the embodiment shown in FIG. 1, the surface of the coarse-grained cloth 10 is roughened, and the surface opposite to the cloth 10 has a lining paper 14 that is breathable and moisture permeable.
is attached. Other parts are the same as those in FIG.
塩化ビニル組成物及びその製造方法の一例を示
せば次の通りである。 An example of a vinyl chloride composition and a method for producing the same is as follows.
例2.
配合成分 重量部
イ 塩化ビニル樹脂
(平均重合度1100)
50部
ロ エラストマ 60部
内訳 塩化ビニル−酢酸ビニル
共重合体……50部
クロロプレインゴム……10部
ハ 可塑剤 DOP 50部
ニ その他の添加物
炭酸カルシユウム 30部
発泡剤:アゾジカルボンアミド 3部
安定剤:Ba−Zn系 3部
上記配合物をミキサーで充分に混合して組成物
とし、カレンダーにて0.50mm厚さのフイルムを成
形し、次にこのフイルムを不布(縦糸、緯糸それ
ぞれ68本/2.54cm)を重ねた状態で、フイルム温
度150〜160℃の温度でラミネートし次に発泡炉中
で200〜220℃の温度で80〜120秒間加熱して発泡
させ、而して発泡炉から出した発泡層11がまた
融軟状態のうちに、凹凸ローラを裏面の布地の側
に当て、表面側にゴムローラを当て、布10と発
泡層11を圧接し、布10を発泡層11に減り込
ませ、布10の糸乃至繊維の一部を発泡層の表裏
双方に露出させる。Example 2. Compounding components Parts by weight Vinyl chloride resin (average degree of polymerization 1100) 50 parts Elastomer 60 parts Breakdown Vinyl chloride-vinyl acetate copolymer...50 parts Chloroprene rubber...10 parts C Plasticizer DOP 50 parts D Other additives Calcium carbonate 30 parts Foaming agent: Azodicarbonamide 3 parts Stabilizer: Ba-Zn type 3 parts The above formulation was thoroughly mixed with a mixer to form a composition, and a film with a thickness of 0.50 mm was made using a calendar. This film is then laminated with non-fabric (68 warp and weft yarns/2.54cm each) at a film temperature of 150-160℃, and then heated in a foaming oven at a temperature of 200-220℃. Then, while the foam layer 11 taken out from the foaming furnace is still in a melted and soft state, a textured roller is applied to the back side of the fabric, a rubber roller is applied to the front side, and the fabric is heated for 80 to 120 seconds to foam. 10 and the foam layer 11 are pressed together, the cloth 10 is reduced into the foam layer 11, and a part of the threads or fibers of the cloth 10 are exposed on both the front and back of the foam layer.
而して、冷却ドラムと接触させて、順次常温ま
で冷却して製品を得た。 Then, the product was brought into contact with a cooling drum and cooled down to room temperature one after another to obtain a product.
発泡積層体は凸部15のところで1.0mmであつ
た。 The foam laminate had a thickness of 1.0 mm at the protrusion 15.
ハ 効果
以上のように構成しているこの考案のものは布
10と発泡層11とは全面で接着積層し、殊に発
泡層11に布10を嵌め込んで物理的に結合し、
かつエラストマの接着力と相まつて、従来の接着
剤使用のレザーと損色ない耐剥離強度を有し、ま
た丈夫である。C. Effect In this device constructed as described above, the cloth 10 and the foam layer 11 are adhesively laminated on the entire surface, and in particular, the cloth 10 is fitted into the foam layer 11 to physically connect them.
Combined with the adhesive strength of the elastomer, it has peel resistance that does not cause discoloration compared to conventional adhesive-based leather, and is also durable.
また布には接着剤を用いないから風合に富み、
殊に粗目の布の繊維乃至糸は表裏双方に露出した
部分があるため、湿気はこの積層体中の前記繊維
乃至糸を介して或はこれら繊維の糸の周りに形成
された隙間を通り抜け、若しくはこれら繊維に吸
室され、壁装材として使用し、壁に接着材で接着
する場合にも、水分の蒸着はこの繊維を介して行
われ、乾操が早く、また前記布10入の発泡層1
1による断熱効果により、結露の発生も殆どな
い。 In addition, since no adhesive is used for the cloth, it has a rich texture.
In particular, since the fibers or threads of coarse cloth have exposed portions on both the front and back sides, moisture passes through the fibers or threads in this laminate or through gaps formed around the fibers. Alternatively, when these fibers are used as wall covering materials and bonded to the wall with an adhesive, moisture is vaporized through these fibers, drying quickly, and layer 1
Due to the heat insulating effect of No. 1, there is almost no condensation.
またこの優れた透湿性は椅子や、衣服に用いて
も、肌むれの度合いが公知の糊付積層体より遥か
に少ない。 Furthermore, due to this excellent moisture permeability, even when used for chairs or clothes, the degree of skin irritation is far less than that of known glued laminates.
また丈夫であるから自動車用座席の椅子のよう
に重量荷重が繰り返し加えられるところに適す
る。 Also, because it is durable, it is suitable for places where heavy loads are repeatedly applied, such as car seats.
(実施例固有の効果)
この実施例1のものを実際の壁装材として使用
したところ、施工時の糊の乾燥は接着材を使用し
たレザーよりも速く、また結路も発生しなかつ
た。(Effects Unique to the Example) When the material of Example 1 was used as an actual wall covering material, the glue dried faster during construction than the leather using adhesive, and no knots occurred.
また透湿性試験をJISZ−0208によつて行つた
ところ次の結果を得た。 In addition, a moisture permeability test was conducted according to JISZ-0208, and the following results were obtained.
従来品1(布地なし) 120g/m2/24時間
従来品2 布地に接着剤を塗布後、
発泡層を形成したもの
350g/m2/24時間
本件考案品 1992g/m2/24時間
透湿性は例1.とほゞ同一であり、剥離強度を行
つたところ次の結果を得た。 Conventional product 1 (without fabric) 120g/m 2 /24 hours Conventional product 2 Foam layer formed after applying adhesive to fabric 350g/m 2 /24 hours Invented product 1992g/m 2 /24 hours Moisture permeability was almost the same as Example 1, and when the peel strength was tested, the following results were obtained.
平均剥離強度(Kg/3cm) 従来品(接着剤使用) タテ 2.5 ヨコ 2.2 本件考案のもの タテ 2.7 ヨコ 2.5 Average peel strength (Kg/3cm) Conventional product (using adhesive) Vertical 2.5 Horizontal 2.2 Invented in this case Vertical 2.7 Horizontal 2.5
図面はこの考案に係るものであり、第1図はこ
の考案の実施例1を示す拡大図、第2図は実施例
2の拡大断面図、第3図は公知例の拡大断面図、
第4図も公知の他の例の拡大断面図である。
図中の主な符号、10……布、11……発泡
層、12……露出部分、13……凹凸模様。
The drawings relate to this invention, and FIG. 1 is an enlarged view showing Embodiment 1 of this invention, FIG. 2 is an enlarged sectional view of Embodiment 2, and FIG. 3 is an enlarged sectional view of a known example.
FIG. 4 is also an enlarged sectional view of another known example. Main symbols in the figure: 10... cloth, 11... foam layer, 12... exposed portion, 13... uneven pattern.
Claims (1)
性を有するエラストマを配合した前記三成分を
含む塩化ビニル組成物からなるシート状物を発
泡直後の融軟状態の発泡層に粗目の布状物を圧
接して、前記布状物の一部の繊維糸が前記発泡
層中にめり込んで、発泡層の表裏に露出した部
分が平均的に分布していることを特徴とする塩
化ビニル樹脂発泡シート状物積層体。 2 前記エラストマとしてはNBR(アクリロニト
リルブタジエンゴム)、CR(クロロプレンゴ
ム)、塩素化ポリエチレンのうちの少なくとも
一種よりなるものであることを特徴とする実用
新案登録請求の範囲第1項記載の塩化ビニル樹
脂発泡シート状物積層体。 3 前記エラストマとして、前記NBR、CR、塩
素化ポリエチレンのうちの少なくとも一種と、
更に塩化ビニルと他のモノマーとの共重合体が
添加してなることを特徴とする実用新案登録請
求の範囲第1項記載の塩化ビニル樹脂発泡シー
ト状物積層体。 4 前記発泡体層はその表面に凹凸模様が施され
たものであることを特徴とする実用新案登録請
求の範囲第1項記載の塩化ビニル樹脂発泡シー
ト状物積層体。 5 前記発泡体層は片面の前記布と共に凹凸模様
が施されているものであることを特徴とする実
用新案登録請求の範囲第1項記載の塩化ビニル
樹脂発泡シート状物積層体。[Claims for Utility Model Registration] 1. Foaming in a melted and softened state immediately after foaming a sheet-like material made of a vinyl chloride composition containing the above three components, which is a mixture of a vinyl chloride resin, a plasticizer, and an elastomer that is compatible with these. A coarse cloth-like material is pressed against the layer, and some of the fiber threads of the cloth-like material sink into the foam layer, so that the exposed parts on the front and back of the foam layer are distributed evenly. PVC resin foam sheet-like laminate. 2. The vinyl chloride resin according to claim 1, wherein the elastomer is made of at least one of NBR (acrylonitrile butadiene rubber), CR (chloroprene rubber), and chlorinated polyethylene. Foam sheet laminate. 3 As the elastomer, at least one of the NBR, CR, and chlorinated polyethylene;
The polyvinyl chloride resin foam sheet laminate according to claim 1, further comprising a copolymer of vinyl chloride and other monomers. 4. The polyvinyl chloride resin foam sheet laminate according to claim 1, wherein the foam layer has an uneven pattern on its surface. 5. The polyvinyl chloride resin foam sheet-like laminate according to claim 1, wherein the foam layer is provided with an uneven pattern together with the cloth on one side.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12685485U JPH0320116Y2 (en) | 1985-08-20 | 1985-08-20 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12685485U JPH0320116Y2 (en) | 1985-08-20 | 1985-08-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6235821U JPS6235821U (en) | 1987-03-03 |
| JPH0320116Y2 true JPH0320116Y2 (en) | 1991-04-30 |
Family
ID=31021053
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12685485U Expired JPH0320116Y2 (en) | 1985-08-20 | 1985-08-20 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0320116Y2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002210851A (en) * | 2001-01-17 | 2002-07-31 | Idemitsu Unitech Co Ltd | Foam laminated sheet and method for producing the same |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7775090B2 (en) * | 2022-01-27 | 2025-11-25 | 株式会社トクヤマ | Foamed vinyl chloride resin sheet and method for producing same |
-
1985
- 1985-08-20 JP JP12685485U patent/JPH0320116Y2/ja not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002210851A (en) * | 2001-01-17 | 2002-07-31 | Idemitsu Unitech Co Ltd | Foam laminated sheet and method for producing the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6235821U (en) | 1987-03-03 |
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