JPH0735637B2 - Breathable waterproof fabric - Google Patents
Breathable waterproof fabricInfo
- Publication number
- JPH0735637B2 JPH0735637B2 JP60162842A JP16284285A JPH0735637B2 JP H0735637 B2 JPH0735637 B2 JP H0735637B2 JP 60162842 A JP60162842 A JP 60162842A JP 16284285 A JP16284285 A JP 16284285A JP H0735637 B2 JPH0735637 B2 JP H0735637B2
- Authority
- JP
- Japan
- Prior art keywords
- cloth
- solvent
- thin film
- less
- fabric
- 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
Links
- 239000004744 fabric Substances 0.000 title claims description 37
- 239000010409 thin film Substances 0.000 claims description 23
- 239000000178 monomer Substances 0.000 claims description 22
- 239000002904 solvent Substances 0.000 claims description 19
- 229920005989 resin Polymers 0.000 claims description 14
- 239000011347 resin Substances 0.000 claims description 14
- 230000005484 gravity Effects 0.000 claims description 11
- 230000009257 reactivity Effects 0.000 claims description 7
- 238000006068 polycondensation reaction Methods 0.000 claims description 5
- 238000012695 Interfacial polymerization Methods 0.000 claims description 2
- 239000010408 film Substances 0.000 description 22
- 239000000243 solution Substances 0.000 description 18
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- 230000035699 permeability Effects 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000002253 acid Substances 0.000 description 9
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000004677 Nylon Substances 0.000 description 5
- 239000004952 Polyamide Substances 0.000 description 5
- -1 aliphatic diamines Chemical class 0.000 description 5
- FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 description 5
- 229920001778 nylon Polymers 0.000 description 5
- 229920002647 polyamide Polymers 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000004984 aromatic diamines Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000000635 electron micrograph Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- IGBBASACHKUXPX-UHFFFAOYSA-N N=C=O.N=C=O.CCC(CO)(CO)CO Chemical compound N=C=O.N=C=O.CCC(CO)(CO)CO IGBBASACHKUXPX-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001334 alicyclic compounds Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- WYTGDNHDOZPMIW-RCBQFDQVSA-N alstonine Natural products C1=CC2=C3C=CC=CC3=NC2=C2N1C[C@H]1[C@H](C)OC=C(C(=O)OC)[C@H]1C2 WYTGDNHDOZPMIW-RCBQFDQVSA-N 0.000 description 1
- 150000001412 amines Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- YMHQVDAATAEZLO-UHFFFAOYSA-N cyclohexane-1,1-diamine Chemical compound NC1(N)CCCCC1 YMHQVDAATAEZLO-UHFFFAOYSA-N 0.000 description 1
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
- OYOFUEDXAMRQBB-UHFFFAOYSA-N cyclohexylmethanediamine Chemical compound NC(N)C1CCCCC1 OYOFUEDXAMRQBB-UHFFFAOYSA-N 0.000 description 1
- FNILDPCCWMWNTE-UHFFFAOYSA-N dicyclohexylmethanediol Chemical compound C1CCCCC1C(O)(O)C1CCCCC1 FNILDPCCWMWNTE-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- PVAONLSZTBKFKM-UHFFFAOYSA-N diphenylmethanediol Chemical compound C=1C=CC=CC=1C(O)(O)C1=CC=CC=C1 PVAONLSZTBKFKM-UHFFFAOYSA-N 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
【発明の詳細な説明】 〈産業上の利用分野〉 本発明は新規透湿性防水布帛に関し、特に連続樹脂薄膜
を有する新規な軽量で風合いの良好な透湿性防水布帛及
びその製造法に関するものである。DETAILED DESCRIPTION OF THE INVENTION <Field of Industrial Application> The present invention relates to a novel breathable waterproof fabric, and more particularly to a novel lightweight breathable waterproof fabric having a continuous resin thin film and having a good texture, and a method for producing the same. .
〈従来の技術〉 従来、連続樹脂薄膜を有し軽量で風合いの良好な透湿性
防水布帛としては、布帛上に微多孔薄膜フイルムをラミ
ネートしたものやグラビヤコーターで繰返しコーテイン
グしたものが知られている。しかしながら、前者は接着
剤層が必要なため、微多孔薄膜フイルムのもつ透湿性が
十分に発揮できないという欠点がある。また、後者は連
続樹脂薄膜とするためにコーテイングを数回繰返す必要
があり、生産性に問題がある。<Prior Art> Conventionally, as a moisture-permeable waterproof cloth having a continuous resin thin film and having a good texture, those in which a microporous thin film is laminated on the cloth and those which are repeatedly coated with a gravure coater are known. . However, since the former requires an adhesive layer, it has a drawback that the moisture permeability of the microporous thin film cannot be sufficiently exhibited. In the latter case, coating is required to be repeated several times to form a continuous resin thin film, which is problematic in productivity.
〈発明が解決しようとする問題点〉 本発明の目的は上記欠点のない透湿性防水布帛を提供す
ることにあり、特に、透湿性に優れ、また生産性にも優
れた連続樹脂薄膜を有し軽量で風合いの良好な透湿性防
水布帛を提供することにある。<Problems to be Solved by the Invention> An object of the present invention is to provide a moisture-permeable waterproof fabric that does not have the above-mentioned drawbacks, and particularly, to have a continuous resin thin film having excellent moisture permeability and also excellent productivity. It is to provide a lightweight, breathable waterproof fabric having a good texture.
〈問題点を解決するための手段〉 本発明の透湿性防水布帛は重縮合または重付加反応性を
有する一方のモノマーを溶媒Aに溶解してなる溶液を布
帛に含浸した後、前記溶媒Aとは相溶性を有せずかつ前
記溶媒Aの比重より小さい比重を有する溶媒Bに重縮合
または重付加反応性を有する他方のモノマーを溶解して
なる溶液に該布帛を接触させて布帛上で界面重合せしめ
ることにより形成される、25μ以下の間隔で高さ10μ以
下の蛇行性のひだ状表面構造を有する膜厚10μ以下の連
続樹脂薄膜を布帛に有することを特徴とする。<Means for Solving the Problems> The moisture-permeable waterproof cloth of the present invention is obtained by impregnating the cloth with a solution prepared by dissolving one monomer having polycondensation or polyaddition reactivity in the solvent A, and then by adding the solvent A to the solution. Is a non-compatible solvent B having a specific gravity smaller than the specific gravity of the solvent A, and the other monomer having polycondensation or polyaddition reactivity is dissolved in the solution B to bring the cloth into contact with the solution to form an interface on the cloth. The fabric is characterized by having a continuous resin thin film having a film thickness of 10 μm or less and having a serpentine fold-like surface structure having a height of 10 μm or less at intervals of 25 μm or less, which is formed by polymerization.
本発明でいう重縮合反応性を有するモノマーの組合わせ
としては、ポリアミドを生成する系、ポリエステルを生
成する系などがあげられる。ポリアミドおよびポリエス
テルを生成する系の酸成分モノマーとしては脂肪族また
は芳香族の二塩基酸ジハライド類などが用いられる。例
えば、アジピン酸、セバシン酸等の脂肪族二塩基酸のジ
ハライド類、テレフタル酸、イソフタル酸、4,4′−ジ
フエニルメタンカルボン酸等の芳香族二塩基酸のジハラ
イド類、シクロヘキサンジカルボン酸、ジシクロヘキシ
ルメタンジカルボン酸等の脂環式二塩基酸のジハライド
類、カルボン酸ハライド残基を少なくとも1つ以上もつ
ポリアミド、ポリエステルのプレポリマーなどである。
これらの酸成分モノマーと重縮合させる対応モノマーと
しては、脂肪族または芳香族のジアミン類、ジオール類
などが用いられる。例えば、ジアミン類としてはエチレ
ンジアミン、トリメチレンジアミン、ヘキサメチレンジ
アミン等の脂肪族ジアミン類、o−,m−,p−フエニレン
ジアミン等の芳香族ジアミン類、シクロヘキサンジアミ
ン、シクロヘキシルメチレンジアミン等の脂環式ジアミ
ン類、アミン残基を少なくとも1つ以上もつポリアミ
ド、ポリウレタンのプレポリマーなどがあげられ、ま
た、ジオール類としては、エチレングリコール、テトラ
エチレングリコール、ポリエチレングリコール等の脂肪
族ジオール類、ヒドロキノン、レゾルシン、ビスフエノ
ールA、ジフエニルメタンジオール等の芳香族ジオール
類、シクロヘキサンジオール、ジシクロヘキシルメタン
ジオール等の脂環式ジオール類、ヒドロキシル残基を少
なくとも1つ以上もつポリエステル、ポリウレタンのプ
レポリマーなどがあげられる。また、縮合反応によつて
生成する酸をNaOHなどのアルカリによつて捕捉すること
により、重合反応性が向上する。Examples of the combination of the monomers having polycondensation reactivity in the present invention include a system for producing a polyamide and a system for producing a polyester. Aliphatic or aromatic dibasic acid dihalides are used as the acid component monomer of the system for producing polyamide and polyester. For example, dihalides of aliphatic dibasic acids such as adipic acid and sebacic acid, terephthalic acid, isophthalic acid, dihalides of aromatic dibasic acids such as 4,4′-diphenylmethanecarboxylic acid, cyclohexanedicarboxylic acid, dicyclohexyl. Examples include dihalides of alicyclic dibasic acids such as methanedicarboxylic acid, polyamides having at least one carboxylic acid halide residue, polyester prepolymers, and the like.
Aliphatic or aromatic diamines and diols are used as the corresponding monomers to be polycondensed with these acid component monomers. For example, as diamines, aliphatic diamines such as ethylenediamine, trimethylenediamine, and hexamethylenediamine, aromatic diamines such as o-, m-, p-phenylenediamine, and alicyclic compounds such as cyclohexanediamine and cyclohexylmethylenediamine. Formula diamines, polyamides having at least one or more amine residues, prepolymers of polyurethane, and the like, and examples of diols include aliphatic diols such as ethylene glycol, tetraethylene glycol, and polyethylene glycol, hydroquinone, and resorcin. , Bisphenol A, aromatic diols such as diphenylmethanediol, alicyclic diols such as cyclohexanediol and dicyclohexylmethanediol, polyester having at least one or more hydroxyl residues Examples include a prepolymer of letane. Further, by trapping the acid generated by the condensation reaction with alkali such as NaOH, the polymerization reactivity is improved.
本発明でいう重付加反応性を有するモノマーの組合わせ
としては、ポリウレタンを生成する系などがあげられ
る。ポリウレタンを生成する系のうち、一方の成分モノ
マーとしては上述のジアミン類およびジオール類がその
まま使用できる。もう一方の成分モノマーとしては、脂
肪族または芳香族のジイソシアネートが好ましく用いら
れる。例えば、ヘキサメチレンジイソシアネート、トリ
メチロールプロパンジイソシアネート等の脂肪族ジイソ
シアネート類、トルエンジイソシアネート、ジフエニル
メタンジイソシアネート等の芳香族ジイソシアネート
類、ジシクロヘキシルメタンジイソシアネート、イソフ
オロンジイソシアネート等の脂環式ジイソシアネート
類、イソシアネート残基を少なくとも1つ以上もつポリ
ウレタンプレポリマーなどである。Examples of the combination of the monomers having polyaddition reactivity in the present invention include a system for producing polyurethane. The above diamines and diols can be used as they are as one of the component monomers in the system for producing polyurethane. An aliphatic or aromatic diisocyanate is preferably used as the other component monomer. For example, hexamethylene diisocyanate, aliphatic diisocyanates such as trimethylolpropane diisocyanate, toluene diisocyanate, aromatic diisocyanates such as diphenylmethane diisocyanate, dicyclohexylmethane diisocyanate, alicyclic diisocyanates such as isofluorone diisocyanate, isocyanate residue Examples include polyurethane prepolymers having at least one or more.
二種以上の混合モノマーを使用する場合は、混合比に対
応する共重合比のポリマー被膜を得ることができる。ま
た、モノマーの選択が自由であるため、通常の加熱成膜
ではフイルム化できない樹脂の被膜も得ることができ
る。特にテレフタル酸ジハライド又はイソフタル酸ジハ
ライドなどの芳香族二塩基酸のジハライドとフエニレン
ジアミンなどの芳香族ジアミンの系では、耐熱性が良好
な芳香族ポリアミドの被覆が得られる。When two or more kinds of mixed monomers are used, a polymer film having a copolymerization ratio corresponding to the mixing ratio can be obtained. Further, since the monomers can be freely selected, it is possible to obtain a resin film which cannot be formed into a film by ordinary heating film formation. Particularly, in the system of a dihalide of an aromatic dibasic acid such as terephthalic acid dihalide or isophthalic acid dihalide and an aromatic diamine such as phenylenediamine, an aromatic polyamide coating having good heat resistance can be obtained.
本発明でいう布帛とは、ポリアミド、ポリエステル、ポ
リアクリルなどの合成繊維およびこれらの改質繊維、羊
毛、絹、木綿、麻などの天然繊維、アセテート、レーヨ
ンなどの半合成繊維など、あるいはこれらの混用繊維か
らなるシート状物であつて、たとえば織編物、不織布な
どをいう。The cloth referred to in the present invention means synthetic fibers such as polyamide, polyester and polyacrylic and modified fibers thereof, natural fibers such as wool, silk, cotton and hemp, semi-synthetic fibers such as acetate and rayon, or the like. A sheet-like material made of mixed fibers, for example, a woven or knitted fabric, a non-woven fabric, or the like.
布帛は通気度が20cc/cm2・秒以下であるものが好まし
い。20cc/cm2・秒よりも大きい通気性を有する布帛で
は、一般に生成する樹脂被膜による被覆が不完全とな
り、十分な耐水性が得られない。The fabric preferably has an air permeability of 20 cc / cm 2 · sec or less. In the case of a fabric having an air permeability of more than 20 cc / cm 2 · sec, the resin film that is generally formed is not completely covered, and sufficient water resistance cannot be obtained.
モノマーを布帛上で重合させる方法は、一方のモノマー
溶液を布帛に含浸した後、その溶媒とは相溶性を有しな
い溶媒に他方のモノマーを溶解した溶液に該布帛を接触
させる界面重合法で行う。The method of polymerizing the monomers on the cloth is performed by an interfacial polymerization method in which the cloth is impregnated with one of the monomer solutions and then the cloth is brought into contact with a solution in which the other monomer is dissolved in a solvent that is incompatible with the solvent. .
モノマーを含有する互いに相溶性を有しない溶液の溶媒
の組み合わせとしては、布帛に含浸する溶液の溶媒の比
重より、一方のモノマー溶液を含浸した布帛に接触させ
る溶液の溶媒の比重が小さいことが重要である。具体的
には、水またはメタノール、エタノール等の低級アルコ
ール類とこれに溶解しない有機溶媒との組み合わせが好
ましく、比重の大きい方の溶媒を用いたモノマー溶液を
布帛に含浸し、比重の小さい方の溶媒を用いたモノマー
溶液に接触させる。特に、モノマーの両溶媒への溶解度
が大きく異なる点から水と炭化水素類またはハロゲン化
炭化水素類との組み合わせが好ましい。いずれの溶媒溶
液を先に布帛に含浸するかについては、布帛の親水性の
程度により決定される。すなわち、布帛の親水性が高い
場合には、水または低級アルコール類の溶媒溶液の方が
好ましく、逆に親油性が高い場合には、有機溶媒溶液の
方が好ましい。It is important that the solvent of the solution containing the monomers that is not compatible with each other has a smaller specific gravity of the solvent of the solution contacting the cloth impregnated with one of the monomer solutions than the specific gravity of the solvent of the solution impregnating the cloth. Is. Specifically, a combination of water or a lower alcohol such as methanol or ethanol and an organic solvent that does not dissolve in it is preferable, and the cloth is impregnated with a monomer solution using a solvent having a higher specific gravity to obtain a solution having a lower specific gravity. Contact the monomer solution with the solvent. In particular, a combination of water and hydrocarbons or halogenated hydrocarbons is preferable because the solubilities of the monomers in both solvents greatly differ. Which solvent solution is impregnated into the fabric first is determined by the degree of hydrophilicity of the fabric. That is, when the cloth has a high hydrophilicity, a solvent solution of water or lower alcohols is preferable, and conversely, when the cloth has a high lipophilicity, an organic solvent solution is preferable.
モノマーの濃度としては0.1M〜2M程度が良い。0.1M以下
では生成樹脂による被覆が不十分となり耐水性が低くな
り、また、2M以上では生成樹脂の付着量が大きくなりす
ぎ、軽量化にならず、また風合いもかたくなる。特に好
ましくは0.3〜1Mである。また、両溶液の濃度は等しい
方がよい。The monomer concentration is preferably about 0.1M to 2M. If it is less than 0.1M, the coating with the generated resin will be insufficient and the water resistance will be low, and if it is more than 2M, the amount of the generated resin attached will be too large and the weight will not be reduced and the texture will be hard. It is particularly preferably 0.3 to 1M. Further, it is preferable that the concentrations of both solutions are equal.
連続樹脂薄膜の膜厚は10μ以下であることが必要であ
る。膜厚が10μより大きい場合は、十分な透湿性が得ら
れず、又、風合いが硬くなり軽量化も達成されない。特
に、透湿性、風合い、軽量化を高いレベルで満足させる
ためには、膜厚が3μ以下であることが好ましい。The thickness of the continuous resin thin film needs to be 10 μm or less. When the film thickness is larger than 10 μ, sufficient moisture permeability cannot be obtained, and the texture becomes hard and weight reduction cannot be achieved. In particular, the film thickness is preferably 3 μm or less in order to satisfy high levels of moisture permeability, texture and weight reduction.
連続樹脂薄膜の膜構造は、表面に25μ以下の間隔で高さ
10μ以下の蛇行性のひだ状構造を有することが透湿性の
点で重要である。本発明において膜厚とは、均一膜厚の
薄膜部分の膜厚とひだ状構造の高さの和を言い、この和
も10μ以下である必要がある。当然のことながら、ひだ
状構造の高さは10μ以下であることが必要である。ま
た、ひだ状構造の間隔は25μ以下であることが必要であ
る。この間隔が25μより大きい場合は、膜強力の向上に
ほとんど効果がなく、耐久性の向上効果が見られない。
本構造においては、ひだ状構造により耐久性を向上させ
ることができるために、薄膜部分をさらに薄くすること
が可能となり、また、表面積が増大するため透湿性を向
上させることができるのである。さらに、ひだ状構造が
蛇行性であるため膜の補強効果がより効果的に発揮され
るのである。The film structure of continuous resin thin film has a height of 25μ or less on the surface.
It is important in terms of moisture permeability to have a meandering pleated structure of 10 μm or less. In the present invention, the film thickness means the sum of the film thickness of the thin film portion having a uniform film thickness and the height of the pleated structure, and this sum also needs to be 10 μm or less. As a matter of course, the height of the pleated structure needs to be 10 μ or less. In addition, it is necessary that the interval of the pleated structure is 25 μ or less. If this interval is larger than 25 μ, there is almost no effect on the improvement of the film strength, and no effect of improving the durability is observed.
In this structure, since the durability can be improved by the pleated structure, the thin film portion can be further thinned, and since the surface area is increased, the moisture permeability can be improved. Furthermore, since the pleated structure is meandering, the reinforcing effect of the membrane is exerted more effectively.
〈作用〉 本発明の連続樹脂薄膜を有する布帛は高い透湿性と防水
布帛性を兼備していると共に、接着層を有さず、耐久性
にも優れており、また製造法としても、一段階で重合と
コーテイングを行うため低コストである。<Function> The cloth having the continuous resin thin film of the present invention has both high moisture permeability and waterproof cloth property, has no adhesive layer and is excellent in durability, and is a one-step manufacturing method. Since the polymerization and coating are performed at low cost.
〈実施例〉 以下の実施例によつて本発明をさらに詳細に説明する。<Example> The present invention will be described in more detail with reference to the following examples.
実施例中の通気量はJIS L1096−1979A法により、フラジ
ール型試験機を用いて測定したものであり、透湿度はJI
S Z−0208法により透湿カツプを用いて測定したもので
ある。また、耐水性はJIS L1092−1977A法(低圧法)に
より測定したものである。膜厚については電子顕微鏡写
真より求めた。The air permeability in the examples is measured by JIS L1096-1979A method using a Frazier type tester, and the water vapor permeability is JI.
It is measured by the SZ-0208 method using a moisture permeable cup. The water resistance is measured by JIS L1092-1977A method (low pressure method). The film thickness was obtained from an electron micrograph.
〈実施例1〉 ナイロン6タフタ(経糸70デニール、12フイラメント、
緯糸70デニール、24フイラメント、織密度タテ120本/i
n、ヨコ90本/in、通気量14.32cc/cm2・秒、透湿度9600g
/m2・24hr、耐水圧0mmH2O)を、イソフタル酸ジクロリ
ドの1Mクロロホルム溶液(クロロホルムの比重:1.489g/
cm3)に浸漬した後、ヘキサメチレンジアミン1M、水酸
化ナトリウム2Mの水溶液(水の比重:1.0g/cm3)の液面
に2分間浮かせた後、水洗、乾燥し、膜厚1μのナイロ
ン6Iの被覆薄膜を形成させた。この布帛の性能は表1に
示した通りであつた。<Example 1> Nylon 6 taffeta (70 denier warp, 12 filament,
Weft 70 denier, 24 filament, weave density vertical 120 pieces / i
n, width 90 pieces / in, ventilation rate 14.32cc / cm 2 · second, moisture permeability 9600g
/ m 2 · 24hr, water pressure resistance 0mmH 2 O), isophthalic acid dichloride 1M chloroform solution (specific gravity of chloroform: 1.489g /
cm 3 ), and then float on the surface of an aqueous solution of hexamethylenediamine 1 M and sodium hydroxide 2 M (specific gravity of water: 1.0 g / cm 3 ) for 2 minutes, then wash with water and dry, nylon with a thickness of 1μ A 6I coating film was formed. The performance of this fabric was as shown in Table 1.
〈比較例1〉 イソフタル酸ジクロリドの濃度を2Mとした以外は実施例
1と同様の処理を行い、膜厚11μのナイロン6Iの被覆薄
膜を形成させた。<Comparative Example 1> The same treatment as in Example 1 was performed except that the concentration of isophthalic acid dichloride was changed to 2 M, to form a nylon 6I coating thin film having a thickness of 11 µm.
〈実施例2〉 イソフタル酸ジクロリドの溶媒を四塩化炭素(比重:1.5
95g/cm3)に変えた以外は実施例1と同様の処理を行
い、膜厚1μの薄膜と高さ9μ、間隔15μのひだ状構造
を有する被覆膜を形成させた。Example 2 A solvent for isophthalic acid dichloride was carbon tetrachloride (specific gravity: 1.5).
The same treatment as in Example 1 was carried out except that the coating film was changed to 95 g / cm 3 ) to form a thin film having a film thickness of 1 μ and a coating film having a pleated structure having a height of 9 μ and an interval of 15 μ.
〈実施例3〉 イソフタル酸ジクロリドの濃度を0.5Mとした以外は実施
例1と同様の処理を行い、膜厚2μの薄膜と高さ5μ、
間隔5μのひだ状構造を有する被覆膜を形成させた。<Example 3> The same treatment as in Example 1 was performed except that the concentration of isophthalic acid dichloride was changed to 0.5M, and a thin film having a film thickness of 2μ and a height of 5μ,
A coating film having a pleated structure with an interval of 5 μ was formed.
〈比較例2〉 イソフタル酸ジクロリド、ヘキサメチレンジアミン、水
酸化ナトリウムの濃度を、0.5M、0.5M、1Mとした以外は
実施例1と同様の処理を行い、膜厚1μの薄膜と高さ5
μ、間隔30μのひだ状構造を有する被覆膜を形成させ
た。Comparative Example 2 The same treatment as in Example 1 was performed except that the concentrations of isophthalic acid dichloride, hexamethylenediamine, and sodium hydroxide were changed to 0.5M, 0.5M, and 1M, and a thin film with a thickness of 1 μm and a height of 5 were used.
A coating film having a pleated structure with a gap of 30 μ was formed.
〈発明の効果〉 a.軽量で風合いがソフトである。<Effect of the invention> a. Light weight and soft texture.
b.防風性、防水性が高い。b. Highly windproof and waterproof.
c.透湿性が高い。c. High moisture permeability.
d.重合と被覆を同時に行うので低コストである。d. Low cost because polymerization and coating are performed simultaneously.
e.布帛外観をそのまま残した被覆膜である。e. A coating film that retains the appearance of the fabric.
f.被覆樹脂の種類が多様である。f. There are various types of coating resins.
図面はいずれも本発明の透湿性防水布帛の繊維の形状と
薄膜との関係を示す電子顕微鏡写真である。 第1図、第2図はそれぞれナイロンタフタ上に膜厚1μ
の薄膜を形成させたもの(実施例1)の表面および断面
を電子顕微鏡で拡大した写真であり、第1図は150倍の
薄膜の表面部分であり、第2図は1000倍のナイロンタフ
タの断面を含む薄膜の断面である。 第3図、第4図はそれぞれ蛇行性のひだ状構造を表面に
有するもの(実施例2)の表面および断面の拡大写真で
あり、第3図は150倍の薄膜の表面部分であり、第4図
は1000倍のナイロンタフタの断面を含む薄膜の断面であ
る。All the drawings are electron micrographs showing the relationship between the shape of the fibers and the thin film of the moisture-permeable waterproof fabric of the present invention. Figures 1 and 2 show a film thickness of 1μ on nylon taffeta, respectively.
2 is an electron microscopic enlarged photograph of the surface and cross section of the thin film of Example 1 (Example 1), and FIG. 1 shows the surface portion of the thin film of 150 times, and FIG. 2 shows the nylon taffeta of 1000 times. It is a cross section of a thin film including a cross section. FIG. 3 and FIG. 4 are enlarged photographs of the surface and cross section of the one having a meandering pleated structure on the surface (Example 2), and FIG. 3 is a surface portion of a thin film of 150 times. Figure 4 shows the cross section of a thin film including the cross section of 1000 times nylon taffeta.
Claims (1)
モノマーを溶媒Aに溶解してなる溶液を布帛に含浸した
後、前記溶媒Aとは相溶性を有せずかつ前記溶媒Aの比
重より小さい比重を有する溶媒Bに重縮合または重付加
反応性を有する他方のモノマーを溶解してなる溶液に該
布帛を接触させて布帛上で界面重合せしめることにより
形成される、25μ以下の間隔で高さ10μ以下の蛇行性の
ひだ状表面構造を有する膜厚10μ以下の連続樹脂薄膜を
布帛上に有することを特徴とする透湿性防水布帛。1. After impregnating a cloth with a solution prepared by dissolving one monomer having polycondensation or polyaddition reactivity in a solvent A, the cloth has no compatibility with the solvent A and a specific gravity of the solvent A. Formed by bringing the cloth into contact with a solution obtained by dissolving the other monomer having polycondensation or polyaddition reactivity in the solvent B having a smaller specific gravity to cause interfacial polymerization on the cloth, at intervals of 25 μm or less. A moisture-permeable waterproof fabric, comprising a continuous resin thin film having a thickness of 10 μm or less and having a meandering pleated surface structure having a height of 10 μm or less on the fabric.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60162842A JPH0735637B2 (en) | 1985-07-25 | 1985-07-25 | Breathable waterproof fabric |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60162842A JPH0735637B2 (en) | 1985-07-25 | 1985-07-25 | Breathable waterproof fabric |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6228475A JPS6228475A (en) | 1987-02-06 |
| JPH0735637B2 true JPH0735637B2 (en) | 1995-04-19 |
Family
ID=15762276
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60162842A Expired - Lifetime JPH0735637B2 (en) | 1985-07-25 | 1985-07-25 | Breathable waterproof fabric |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0735637B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5509142A (en) * | 1993-06-30 | 1996-04-23 | Kimberly-Clark Corporation | Raised arm coveralls |
| GB2285411B (en) * | 1993-12-22 | 1997-07-16 | Kimberly Clark Co | Process of manufacturing a water-based adhesive bonded, solvent resistant protective laminate |
| US5487189A (en) * | 1994-03-16 | 1996-01-30 | Kimberly-Clark Corporation | Coveralls having reduced seams and seamless shoulder construction and method of manufacture |
| US5770529A (en) * | 1995-04-28 | 1998-06-23 | Kimberly-Clark Corporation | Liquid-distribution garment |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55107578A (en) * | 1979-01-29 | 1980-08-18 | Nitto Boseki Co Ltd | Gloss imparting method of knitted and woven fabric |
| JPS61201075A (en) * | 1985-03-05 | 1986-09-05 | 東レ株式会社 | Treatment of cloth |
-
1985
- 1985-07-25 JP JP60162842A patent/JPH0735637B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6228475A (en) | 1987-02-06 |
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