JPH05222677A - Coated cloth and its production - Google Patents
Coated cloth and its productionInfo
- Publication number
- JPH05222677A JPH05222677A JP3201310A JP20131091A JPH05222677A JP H05222677 A JPH05222677 A JP H05222677A JP 3201310 A JP3201310 A JP 3201310A JP 20131091 A JP20131091 A JP 20131091A JP H05222677 A JPH05222677 A JP H05222677A
- Authority
- JP
- Japan
- Prior art keywords
- coating
- moisture permeability
- resin
- cloth
- 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.)
- Granted
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 58
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 238000000576 coating method Methods 0.000 claims abstract description 41
- 239000011248 coating agent Substances 0.000 claims abstract description 38
- 239000000843 powder Substances 0.000 claims abstract description 23
- 229920005749 polyurethane resin Polymers 0.000 claims abstract description 20
- 239000002245 particle Substances 0.000 claims abstract description 17
- 229920001059 synthetic polymer Polymers 0.000 claims abstract description 16
- 229920005989 resin Polymers 0.000 claims description 36
- 239000011347 resin Substances 0.000 claims description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
- 230000035699 permeability Effects 0.000 claims description 28
- 239000000835 fiber Substances 0.000 claims description 12
- 239000011148 porous material Substances 0.000 claims description 11
- 238000005345 coagulation Methods 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 230000015271 coagulation Effects 0.000 claims description 2
- 238000004078 waterproofing Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 21
- 238000005299 abrasion Methods 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 4
- 150000002681 magnesium compounds Chemical class 0.000 abstract description 2
- 150000003377 silicon compounds Chemical class 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 23
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- 239000005871 repellent Substances 0.000 description 13
- 230000002940 repellent Effects 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- -1 polyethylene terephthalate Polymers 0.000 description 9
- 239000000243 solution Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 239000012948 isocyanate Substances 0.000 description 7
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 229920002994 synthetic fiber Polymers 0.000 description 5
- 239000012209 synthetic fiber Substances 0.000 description 5
- 229910002012 Aerosil® Inorganic materials 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 239000000395 magnesium oxide Substances 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 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 2
- 229920000742 Cotton Polymers 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 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 2
- 238000005406 washing Methods 0.000 description 2
- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- WLDHEUZGFKACJH-UHFFFAOYSA-K amaranth Chemical compound [Na+].[Na+].[Na+].C12=CC=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(O)=C1N=NC1=CC=C(S([O-])(=O)=O)C2=CC=CC=C12 WLDHEUZGFKACJH-UHFFFAOYSA-K 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は,雨衣,外衣等の各種衣
料用として用いられる透湿性能および防水性能の優れた
コーテング布帛およびその製造方法に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a coating cloth excellent in moisture permeability and waterproofing, which is used for various kinds of clothes such as rain clothes and outer clothes, and a method for producing the same.
【0002】[0002]
【従来の技術】従来から,湿式あるいは乾式コーテイン
グ加工法により得られるコーテイング布帛は,樹脂層が
有孔のものと無孔のものが知られている。一般的に樹脂
層が有孔のとき,優れた透湿性能は得やすいが,防水性
能は不十分となりやすく,逆に樹脂層が無孔のときに
は,優れた防水性能は得やすいが,透湿性能は不十分と
なりやすい。例えば,ポリウレタン樹脂の湿式コーテイ
ング加工法により得られるコーテイング布帛は,元来防
水性能は優れているが,透湿性能が不十分なので,透湿
性能を向上させるためにアニオン系界面活性剤,ノニオ
ン系界面活性剤,親水性高分子等を併用するのが常であ
る。しかし,得られるコーテイング布帛の透湿性能は十
分ではなく,かつ防水性能をかなり低下させ,結果とし
て両者ともに十分な性能を満足させることができていな
い。2. Description of the Related Art Conventionally, it has been known that a coating cloth obtained by a wet or dry coating processing method has a resin layer with a hole and a resin layer without a hole. Generally, when the resin layer is perforated, excellent moisture permeability is easily obtained, but waterproof performance tends to be insufficient. Conversely, when the resin layer is non-perforated, excellent waterproof performance is easily obtained, but moisture permeability is Performance tends to be insufficient. For example, the coating cloth obtained by the wet coating method of polyurethane resin has originally excellent waterproof performance, but since the moisture permeability is insufficient, in order to improve the moisture permeability, an anionic surfactant and a nonionic surfactant are used. It is usual to use a surfactant, hydrophilic polymer, etc. together. However, the moisture permeability of the obtained coated fabric is not sufficient, and the waterproof performance is considerably deteriorated, and as a result, both cannot satisfy the sufficient performance.
【0003】近年,両者の欠点を補う目的で,繊維布帛
上にまず有孔の高透湿樹脂層を形成し,次に該樹脂層上
に無孔の樹脂層を形成させ,優れた透湿性能と防水性能
を得る方法が試みられているが,この方法でも無孔の樹
脂層を薄く塗布したとしても透湿性能が極端に低下し,
その結果,優れた透湿性能と防水性能を両立させること
は難しいのが現状である。また,この場合には,コーテ
イングを2回行うので,加工コストの点でも不利であ
る。In recent years, for the purpose of compensating for both defects, a highly moisture-permeable resin layer having pores is first formed on a fiber cloth, and then a resin layer having no pores is formed on the resin layer to obtain excellent moisture permeability. Although a method of obtaining performance and waterproof performance has been attempted, even with this method, even when a thin non-porous resin layer is applied, the moisture permeability is extremely lowered,
As a result, it is currently difficult to achieve both excellent moisture permeability and waterproof performance. Further, in this case, coating is performed twice, which is also disadvantageous in terms of processing cost.
【0004】一方,特開昭58−4873号公報および
特公昭62−53632号公報には,二酸化ケイ素を主
成分とする多孔性粒子を含むポリウレタン樹脂皮膜を形
成せしめ,次にパーフルオロアルキル基を有する撥水剤
を付与して透湿性防水布帛を得る加工方法が提案されて
いるが,いずれの方法においても十分な透湿性能は得ら
れていない。On the other hand, in JP-A-58-4873 and JP-B-62-53632, a polyurethane resin film containing porous particles containing silicon dioxide as a main component is formed, and then a perfluoroalkyl group is added. A processing method has been proposed in which a water-repellent agent is added to obtain a moisture-permeable waterproof cloth, but none of them has sufficient moisture permeability.
【0005】さらに,特開平2−251672号公報に
は,150Åより小さい微細孔を有し,かつ表面積20
0m2/g以上の二酸化ケイ素,酸化チタン等の無機多
孔性粒子を高濃度に層状分散した樹脂層を介在させたポ
リエステルコーテイング布帛の加工方法が提案されてい
るが,この発明の目的は,分散染料の移行性を防止する
ものにすぎず,十分な透湿性能は得られていない。Further, Japanese Patent Application Laid-Open No. 2-251672 discloses that it has fine pores smaller than 150Å and has a surface area of 20.
A method of processing a polyester coating fabric with a resin layer in which inorganic porous particles of 0 m 2 / g or more, such as silicon dioxide and titanium oxide, are layered and dispersed in a high concentration has been proposed. It only prevents migration of the dye, and does not have sufficient moisture permeability.
【0006】[0006]
【発明が解決しようとする課題】本発明は,このような
現状に鑑みて行われたもので,優れた透湿性能と防水性
能を兼ね備えたコーテイング布帛を得ることを目的とす
るものである。The present invention has been made in view of the above circumstances, and an object thereof is to obtain a coating cloth having both excellent moisture permeability and waterproof performance.
【0007】[0007]
【課題を解決するための手段】本発明は,上記目的を達
成するもので,次の構成よりなるものである。すなわち
本発明は,「繊維布帛上にポリウレタン樹脂主体の合成
重合体からなる有孔の樹脂層を有し,該樹脂層中に実質
的に無孔で平均粒径が0.1μm以下の無機微粉末を1%
以上含有し,6000g/m2 ・24hrs 以上の透湿度
と0.6kg/cm2 以上の耐水圧を有することを特徴とする
透湿性能および防水性能の優れたコーテイング布帛」並
びに「繊維布帛に,実質的に無孔で平均粒径0.1μm以
下の無機微粉末を樹脂固形分に対して1%以上含むポリ
ウレタン樹脂主体の合成重合体溶液を塗布し,しかる後
に水中に浸漬して樹脂分の湿式凝固を行うことを特徴と
する透湿性能および防水性能の優れたコーテイング布帛
の製造方法」を要旨とするものである。SUMMARY OF THE INVENTION The present invention achieves the above object and has the following configuration. That is, the present invention provides that “a porous resin layer made of a synthetic polymer mainly composed of a polyurethane resin is provided on a fiber cloth, and the resin layer is substantially non-porous and has an average particle size of 0.1 μm or less. 1% powder
"Coating fabric with excellent moisture permeability and waterproof performance, characterized by having a moisture permeability of 6000 g / m 2 · 24 hrs or more and a water pressure resistance of 0.6 kg / cm 2 or more" and "fiber fabric, A polyurethane polymer-based synthetic polymer solution containing substantially no pores and an inorganic fine powder having an average particle size of 0.1 μm or less in an amount of 1% or more based on the resin solid content is applied, and then immersed in water to dilute the resin content. A method for producing a coated fabric having excellent moisture permeability and waterproof performance, which is characterized by performing wet coagulation ".
【0008】以下,本発明について詳細に説明を行う。
本発明におけるコーテング布帛の特徴は,ポリウレタン
樹脂主体の合成重合体の極性有機溶剤溶液中に無機微粉
末を均一分散させて塗布し,次いで,水中に浸漬して樹
脂皮膜を形成する,いわゆる湿式コーテイング法によっ
て製造し,基布となる繊維布帛上に,ポリウレタン樹脂
主体の合成重合体が本来もっている防水性能を低下させ
ることなく,微細で有孔数の多い高透湿性の樹脂層を得
るところにある。The present invention will be described in detail below.
The coating fabric of the present invention is characterized in that a fine inorganic powder is uniformly dispersed and applied in a polar organic solvent solution of a synthetic polymer mainly composed of polyurethane resin and then immersed in water to form a resin film, that is, a so-called wet coating. A method for producing a fine, highly moisture-permeable resin layer with a large number of pores on a fibrous fabric as a base fabric, which is manufactured by the method, without deteriorating the waterproof performance originally possessed by a polyurethane resin-based synthetic polymer. is there.
【0009】本発明で用いられる実質的に無孔の無機微
粉末としては,二酸化ケイ素,炭化ケイ素,窒化ケイ素
等のケイ素化合物,酸化マグネシウム,水酸化マグネシ
ウム,硫酸マグネシウム等のマグネシウム化合物または
これらの粒子表面変性物のうちの少なくとも1種が用い
られるが,中でも乾式法で製造される二酸化ケイ素が実
質的に無孔の微粉末として最も有効である。The substantially non-porous inorganic fine powder used in the present invention includes silicon compounds such as silicon dioxide, silicon carbide and silicon nitride, magnesium compounds such as magnesium oxide, magnesium hydroxide and magnesium sulfate, or particles thereof. At least one of the surface modified products is used, and among them, silicon dioxide produced by a dry method is most effective as a fine powder having substantially no pores.
【0010】使用する無機微粉末の大きさは,平均粒径
が0.1μm以下であることが必要であり,0.05μm以
下にすると,効果の点でより一層好ましい。粒径が0.1
μmより大きいと,得られるコーテイング布帛の透湿膜
の孔径が大きくなりすぎ,防水性能を低下させるので好
ましくない。The size of the inorganic fine powder used is required to have an average particle size of 0.1 μm or less, and a particle size of 0.05 μm or less is more preferable in terms of effects. Particle size is 0.1
If it is larger than μm, the pore size of the moisture permeable membrane of the obtained coating fabric becomes too large, and the waterproof performance is deteriorated, which is not preferable.
【0011】また,無機微粉末は,ポリウレタン樹脂主
体の合成重合体からなる樹脂層に対し,均一に1%以上
含有していることが必要であり,さらに好ましくは3%
以上がよい。1%未満では,得られるコーテイング布帛
の透湿膜の有孔数が少なくなり,高透湿性能が得られな
い。It is necessary that the inorganic fine powder is uniformly contained in the resin layer composed of a synthetic polymer mainly composed of polyurethane resin in an amount of 1% or more, more preferably 3%.
The above is good. When it is less than 1%, the number of pores of the moisture permeable membrane of the obtained coated fabric is small, and high moisture permeability cannot be obtained.
【0012】本発明で用いられる繊維布帛としては,ナ
イロン6やナイロン66で代表されるポリアミド系合成
繊維,ポリエチレンテレフタレートで代表されるポリエ
ステル系合成繊維,ポリアクリロニトリル系合成繊維,
ポリビニルアルコール系合成繊維,トリアセテート等の
半合成繊維あるいはナイロン6/木綿,ポリエチレンテ
レフタレート/木綿等の混合繊維からなる織物,編物,
不織布等を挙げることができる。The fiber cloth used in the present invention includes polyamide synthetic fibers represented by nylon 6 and nylon 66, polyester synthetic fibers represented by polyethylene terephthalate, polyacrylonitrile synthetic fibers,
Woven and knitted fabrics made of polyvinyl alcohol synthetic fibers, semi-synthetic fibers such as triacetate, or mixed fibers such as nylon 6 / cotton, polyethylene terephthalate / cotton, etc.
Nonwoven fabrics and the like can be mentioned.
【0013】本発明では,上記の繊維布帛に撥水剤処理
を施したものを用いてもよい。これは樹脂溶液の布帛内
部への浸透を防ぐための一手段である。この場合の撥水
剤としては,パラフイン系撥水剤やポリシロキサン系撥
水剤,フツ素系撥水剤等の公知のものでよく,その処理
も一般に行われているパデイング法,スプレー法等の公
知の方法で行えばよい。特に良好な撥水性を必要とする
場合には,フツ素系撥水剤を使用し,例えば,アサヒガ
ード730(フツ素系撥水剤エマルジヨン,旭硝子株式
会社製)を5%の水分散液でパデイング(絞り率35
%)後,160℃で1分間の熱処理を行う方法等によっ
て行えばよい。In the present invention, the above fiber cloth may be treated with a water repellent agent. This is one means for preventing the penetration of the resin solution into the fabric. In this case, the water repellent may be a known one such as a paraffin water repellent, a polysiloxane water repellent, and a fluorine water repellent, and the treatment thereof is generally performed such as padding method and spray method. The known method may be used. When particularly good water repellency is required, a fluorine-based water repellent is used, for example, Asahi Guard 730 (fluorine-based water repellent Emulsion, manufactured by Asahi Glass Co., Ltd.) in a 5% aqueous dispersion. Padding (drawing ratio 35
%) And then heat treatment at 160 ° C. for 1 minute.
【0014】本発明のコーテイング布帛においては,上
記の繊維布帛上に無機微粉末を含むポリウレタン樹脂主
体の合成重合体溶液を湿式コーテイング法により塗布す
る。ここでいうポリウレタン樹脂主体の合成重合体と
は,ポリウレタン成分を50〜100%含むものをい
い,その他の合成重合体としては,例えば,ポリアクリ
ル酸,ポリ塩化ビニル,ポリスチレン,ポリブタジエ
ン,ポリアミノ酸等やそれらの共重合体等を50%未満
の範囲で含んでいてもよい。In the coating cloth of the present invention, a synthetic polymer solution mainly composed of a polyurethane resin containing inorganic fine powder is applied onto the above-mentioned fiber cloth by a wet coating method. The synthetic polymer mainly composed of polyurethane resin as used herein means one containing 50 to 100% of a polyurethane component, and other synthetic polymers include, for example, polyacrylic acid, polyvinyl chloride, polystyrene, polybutadiene, polyamino acid, etc. Or their copolymers may be contained in the range of less than 50%.
【0015】ポリウレタン樹脂は,ポリイソシアネート
とポリオールを反応せしめて得られる共重合体であり,
イソシアネート成分として,芳香族ジイソシアネート,
脂肪族ジイソシアネートおよび脂環族ジイソシアネート
の単独またはこれらの混合物を用い,例えば,トリレン
2,4−ジイソシアネート,4,4'−ジフエニルメタンジ
イソシアネート,1,6−ヘキサンジイソシアネート,1,
4−シクロヘキサンジイソシアネート等を用い,また,
ポリオール成分としては,ポリエーテルポリオール,ポ
リエステルポリオールを用い,ポリエーテルポリオール
は,ポリエチレングリコール,ポリプロピレングリコー
ル,ポリテトラメチレングリコール等を用い,ポリエス
テルポリオールは,エチレングリコール,プロピレング
リコール等のジオールとアジピン酸,セバチン酸等の2
塩基酸との反応生成物やカプロラクトン等の開環重合物
を用いる。Polyurethane resin is a copolymer obtained by reacting polyisocyanate and polyol,
As the isocyanate component, aromatic diisocyanate,
Using aliphatic diisocyanates and alicyclic diisocyanates alone or in a mixture thereof, for example, trilene
2,4-diisocyanate, 4,4'-diphenylmethane diisocyanate, 1,6-hexane diisocyanate, 1,
4-cyclohexane diisocyanate, etc.,
Polyether polyol and polyester polyol are used as the polyol component, polyethylene glycol, polypropylene glycol, polytetramethylene glycol and the like are used as the polyether polyol, and diols such as ethylene glycol and propylene glycol and adipic acid and sebacine are used as the polyester polyol. 2 such as acid
A reaction product with a basic acid or a ring-opening polymer such as caprolactone is used.
【0016】また,無機微粉末を含む上記のポリウレタ
ン樹脂主体の合成重合体溶液は,通常のコーテイング方
法,例えば,ナイフコータ,コンマコータ,リバースコ
ータ等を用いて適宜コーテイングを行えばよいが,目的
とする0.6kg/cm2 以上の耐水圧を得るためには,繊維
布帛のコーテイング面の平滑性や通気度(JIS L−
1096法)により異なるが,一般的には樹脂皮膜重量
が5g/m2 以上,好ましくは10g/m2 以上になる
ように塗布量を調節してコーテイングを行うとよい。The above-mentioned polyurethane polymer-based synthetic polymer solution containing the inorganic fine powder may be appropriately coated using a conventional coating method, for example, a knife coater, a comma coater, a reverse coater or the like. In order to obtain a water pressure resistance of 0.6 kg / cm 2 or more, the smoothness and air permeability (JIS L-
1096 method) by different, generally resin film weight 5 g / m 2 or more, may preferably carry out the coating by adjusting the coating amount to be 10 g / m 2 or more.
【0017】本発明では,樹脂層と繊維布帛間の耐剥離
性を向上させる目的で,樹脂あるいは繊維布帛との親和
性の高い化合物を併用してもよく,その化合物としてイ
ソシアネート化合物を併用するとよい。イソシアネート
化合物としては,2,4−トリレ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,イソフオロンジイソ
シアネート,ヘキサメチレンイソシアネートまたはこれ
らのジイソシアネート類3モルと活性水素を含有する化
合物(例えば,トリメチロールプロパン,グリセリン
等)1モルとの付加反応によって得られるトリイソシア
ネート類が使用できる。上記のイソシアネート類は,イ
ソシアネート基が遊離した形のものであっても,あるい
はフエノール,メチルエチルケトオキシム等を付加させ
ることにより安定させ,その後の熱処理によりブロツク
を解離させる形のものであっても,いずれでも使用で
き,作業性や用途等により適宜使い分ければよい。In the present invention, for the purpose of improving the peeling resistance between the resin layer and the fiber cloth, a compound having a high affinity for the resin or the fiber cloth may be used in combination, and an isocyanate compound may be used in combination as the compound. .. As the isocyanate compound, 2,4-tolylene diisocyanate, diphenylmethane diisocyanate, isophorone diisocyanate, hexamethylene isocyanate or a compound containing 3 mol of these diisocyanates and active hydrogen (eg, trimethylolpropane, glycerin, etc.) 1 Triisocyanates obtained by addition reaction with moles can be used. The above-mentioned isocyanates may be in a form in which an isocyanate group is released, or in a form in which a block is dissociated by a subsequent heat treatment after being stabilized by adding phenol, methylethylketoxime or the like. However, it can be used, and it may be appropriately used depending on workability and purpose.
【0018】イソシアネート化合物を使用する際の使用
量としては,ポリウレタン樹脂主体の合成重合体に対し
て0.1〜10重量%の割合で使用することが望ましい。
使用量が0.1%未満であれば,布帛に対する樹脂層の接
着力が低く,また,10%を超えると,風合が硬化する
傾向が認められるようになるので好ましくない。The amount of the isocyanate compound used is preferably 0.1 to 10% by weight based on the synthetic polymer mainly composed of the polyurethane resin.
If the amount used is less than 0.1%, the adhesive force of the resin layer to the fabric is low, and if it exceeds 10%, the texture tends to harden, which is not preferable.
【0019】上述のポリウレタン主体の合成重合体から
なる樹脂液を繊維布帛に塗布した後,本発明では,0〜
30℃の水中に0.5〜10分間浸漬して樹脂分の湿式凝
固を行う。以下,40〜60℃の温水中で5〜15分間
の洗浄後,通常の方法で乾燥する。After the resin liquid consisting of the above-mentioned polyurethane-based synthetic polymer is applied to the fiber cloth, in the present invention,
The resin component is wet-solidified by immersing it in water at 30 ° C. for 0.5 to 10 minutes. Thereafter, after washing in warm water of 40 to 60 ° C. for 5 to 15 minutes, it is dried by a usual method.
【0020】本発明において,防水性をさらに向上させ
る目的で,湿式コーテイング後にコーテイング布帛に撥
水処理を行ってもよい。撥水処理に際しては,前述のよ
うな一般に実施されている公知の撥水処理方法を採用す
ればよい。In the present invention, for the purpose of further improving waterproofness, the coating fabric may be subjected to a water repellent treatment after the wet coating. For the water repellent treatment, a publicly known well-known water repellent treatment method as described above may be adopted.
【0021】[0021]
【作 用】本発明のコーテイング布帛は,ポリウレタン
樹脂主体の合成重合体の樹脂層中に実質的に無孔で平均
粒径が0.1μm以下の無機微粉末を含有せしめることに
より,優れた透湿性能と防水性能を付与せしめたもので
ある。何故に平均粒径0.1μm以下の無機微粉末を含有
せしめることにより優れた透湿性能と防水性能をともに
得ることができるのか明らかではないが,本発明者らは
一応次のように推測している。[Working] The coating fabric of the present invention has an excellent permeability by containing inorganic fine powder having substantially no pores and an average particle size of 0.1 μm or less in the resin layer of a synthetic polymer mainly composed of polyurethane resin. It is a product that has been given wet performance and waterproof performance. It is not clear why it is possible to obtain both excellent moisture permeability and waterproof performance by including an inorganic fine powder having an average particle size of 0.1 μm or less, but the present inventors presume as follows. ing.
【0022】すなわち,実質的に無孔で平均粒径が0.1
μm以下の無機微粉末を均一分散させたポリウレタン樹
脂主体の合成重合体溶液を布帛にコーテイングして湿式
凝固を行うと,ポリウレタン樹脂はその特有のポーラス
構造を形成すると同時に,溶液中には無機微粉末を均一
にミクロ分散させているため,無機微粉末と凝固しよう
とする樹脂との界面で微妙な凝固速度のずれが生じ,そ
の結果,防水性能を低下させずに透湿性能を大幅に向上
させる0.1μm以下の微細な有孔を多数付与することが
できるようになるものと推測される。That is, it is substantially non-porous and has an average particle size of 0.1.
When wet-coagulation is performed by coating a cloth with a synthetic polymer solution consisting mainly of a polyurethane resin in which inorganic fine powder of μm or less is uniformly dispersed, the polyurethane resin forms its unique porous structure, and at the same time, the inorganic fine particles are contained in the solution. Since the powder is uniformly micro-dispersed, a slight deviation in the solidification rate occurs at the interface between the inorganic fine powder and the resin that is about to solidify, and as a result, the moisture permeability is greatly improved without reducing the waterproof performance. It is presumed that it becomes possible to provide a large number of fine pores having a size of 0.1 μm or less.
【0023】本発明では,形成された微細な有孔により
透湿性能が向上しているので,高透湿性防水布帛に特有
の,着用時に圧力が加わったとき問題が発生しやすい,
漏水性に対しても非常に有効である。さらに,本発明の
無機微粉末は,樹脂層の表層から下層まで全体に均一に
存在しているので,樹脂層表面はポリウレタン樹脂特有
のぬめり感を消し,ドライタツチにするとともに,樹脂
層全体の耐摩耗性と接着強度が向上する。In the present invention, since the moisture permeation performance is improved by the formed fine perforations, a problem peculiar to the highly moisture-permeable waterproof fabric is likely to occur when pressure is applied during wearing,
It is also very effective against water leakage. Furthermore, since the inorganic fine powder of the present invention is evenly present from the surface layer to the lower layer of the resin layer, the surface of the resin layer eliminates the slimy feeling peculiar to the polyurethane resin and makes dry touch, and at the same time, the resistance of the entire resin layer is improved. Abrasion resistance and adhesive strength are improved.
【0024】[0024]
【実施例】以下,実施例により本発明をさらに具体的に
説明するが,実施例におけるコーテイング布帛の性能の
測定は,次の方法で行った。 (1)耐水圧 JIS L−1092(高水圧法) (2)透湿度 JIS L−1099(A−1法) (3)漏水性 ブンデスマン法(L−1092参考試
験法)に準じて行い,60分後の漏水量を測定。 (4)摩耗強力 JIS L−1084(A−1法) (5)剥離強度 コーテイング面に,ホツトメルトテー
プを経方向に接着して,JIS L−1089法に準じ
て測定。EXAMPLES The present invention will be described in more detail with reference to the following examples. The performance of the coated fabric in the examples was measured by the following method. (1) Water pressure resistance JIS L-1092 (high water pressure method) (2) Water vapor permeability JIS L-1099 (A-1 method) (3) Water leakage Performed according to the Bundesmann method (L-1092 reference test method), Measure the amount of water leakage after 60 minutes. (4) Abrasion strength JIS L-1084 (method A-1) (5) Peel strength A hot melt tape was adhered to the coating surface in the longitudinal direction, and measured according to JIS L-1089 method.
【0025】実施例1 経糸,緯糸の双方にナイロンハイマルチフイラメント7
0デニール68フイラメントを用いた経糸密度120本
/インチ,緯糸密度90本/インチの平織物を製織し,
通常の方法で精練および染色(三菱化成株式会社製,酸
性染料のDiacidFast Red 3BL 2%owf)を行った後,
フツ素系撥水剤エマルジヨンのアサヒガード710(旭
硝子株式会社製)5%水溶液でパデイング(絞り率35
%)して乾燥後,160℃で1分間の熱処理を行った。
次に,鏡面ロールをもつカレンダー加工機を用いて,温
度170℃,圧力30kg/cm2 ,速度20m/分の条件
でカレンダー加工を行い,コーテイング用の基布を得
た。Example 1 Nylon high multifilament 7 for both warp and weft
Weaving a plain woven fabric with a warp density of 120 yarns / inch and a weft yarn density of 90 yarns / inch using a 0 denier 68 filament,
After performing scouring and dyeing (manufactured by Mitsubishi Kasei Co., Ltd., acid dye Diacid Fast Red 3BL 2% owf) in the usual way,
Asahi guard 710 (made by Asahi Glass Co., Ltd.) of fluorine-based water repellent Emulsion is padded with a 5% aqueous solution (squeeze ratio 35
%) And dried, and then heat-treated at 160 ° C. for 1 minute.
Next, using a calendering machine having a mirror-finished roll, calendering was carried out under conditions of a temperature of 170 ° C., a pressure of 30 kg / cm 2 and a speed of 20 m / min to obtain a base fabric for coating.
【0026】ここで,下記処方1に示す組成で固形分濃
度25%のポリウレタン樹脂溶液を,ナイフオーバーロ
ールコータを用いて上記基布のカレンダー面に塗布量8
0g/m2 にて塗布した後,直ちに15℃の水中に1分
間浸漬して樹脂分を凝固させ,続いて,50℃の温水中
で10分間の洗浄を行い,乾燥し,無機微粉末を11%
含有する樹脂層を形成した。Here, a polyurethane resin solution having a composition shown in the following formulation 1 and a solid content concentration of 25% was applied to the calender surface of the base cloth with a knife over roll coater in an amount of 8
Immediately after application at 0 g / m 2 , it is immersed in water at 15 ° C for 1 minute to solidify the resin component, followed by washing in warm water at 50 ° C for 10 minutes and drying to obtain an inorganic fine powder. 11%
The containing resin layer was formed.
【0027】処方1 レザミンCU−4550 100部 (大日精化工業株式会社製,エステル型ポリウレタン樹
脂) レザミンX 1部 (大日精化工業株式会社製,イソシアネート化合物) N・N−ジメチルホルムアミド 25部 アエロジル#130 3部 (日本アエロジル株式会社製,平均粒径16nmのSi
O2粉末)Prescription 1 Resamine CU-4550 100 parts (Dainichi Seika Kogyo Co., Ltd., ester type polyurethane resin) Resamine X 1 part (Dainichi Seika Kogyo Co., Ltd., isocyanate compound) N / N-dimethylformamide 25 parts Aerosil # 130 3 parts (Nihon Aerosil Co., Ltd., Si with an average particle size of 16 nm
O 2 powder)
【0028】次にグラビアコータにてコーテイング面を
撥水処理すべく,アサヒガード 710の5%水溶液でグラ
ビアコーテイングし,続いて,マングルで絞り(絞り率
40%),乾燥後,160℃で1分間の熱処理を行い,
本発明のコーテイング布帛を得た。Next, in order to make the coated surface water-repellent with a gravure coater, gravure coating was performed with a 5% aqueous solution of Asahi Guard 710, followed by squeezing with a mangle (squeeze ratio of 40%) and drying, followed by 1 ° C at 160 ° C. Heat treatment for a minute,
A coating fabric of the present invention was obtained.
【0029】本発明との比較のため,本実施例において
処方1からアエロジル#130を除くほかは,本実施例
と全く同一の方法により比較用のコーテイング布帛(比
較例1とする)を得た。さらに,本発明との比較のた
め,本実施例の処方1においてアエロジル#130に代
えてNipsil VN3(日本シリカ工業株式会社
製,平均粒径16nmの湿式法微多孔性SiO2粉末)を
同量使用するほかは,本実施例と全く同一の方法により
比較用のコーテイング布帛(比較例2とする)を得た。For comparison with the present invention, a comparative coating fabric (referred to as Comparative Example 1) was obtained in the same manner as in this Example except that Aerosil # 130 was omitted from Formulation 1 in this Example. .. Further, for comparison with the present invention, in the formulation 1 of this example, the same amount of Nipsil VN3 (manufactured by Nippon Silica Industry Co., Ltd., wet method microporous SiO 2 powder having an average particle size of 16 nm) was used instead of Aerosil # 130. A coating fabric for comparison (referred to as Comparative Example 2) was obtained by the same method as in this example except that it was used.
【0030】本発明および比較例1,2のコーテイング
布帛の性能を測定,評価し,その結果を合わせて表1に
示した。The performances of the coating fabrics of the present invention and Comparative Examples 1 and 2 were measured and evaluated, and the results are shown in Table 1.
【0031】[0031]
【表1】 [Table 1]
【0032】表1に示す結果から明らかなように,本発
明のコーテイング布帛は,優れた耐水圧と透湿度を有す
るとともに,従来高透湿性防水布帛がもっていた漏水性
の欠点に対しても有効であり,かつ耐摩耗性,耐剥離性
も良好であることがわかる。As is clear from the results shown in Table 1, the coating fabric of the present invention has excellent water pressure resistance and moisture permeability, and is also effective against the drawback of water leakage which the conventional highly moisture permeable waterproof fabric has. It is also understood that the wear resistance and peeling resistance are also good.
【0033】実施例2 上述の実施例1において,コーテイング液の処方1に代
えて下記処方2を用いるほかは,実施例1と全く同一の
方法により本発明のコーテイング布帛を得た。コーテイ
ング樹脂層の無機微粉末含有量は17%であった。Example 2 A coating fabric of the present invention was obtained in the same manner as in Example 1 except that the following formulation 2 was used in place of the formulation 1 of the coating liquid in the above example 1. The inorganic fine powder content of the coating resin layer was 17%.
【0034】処方2 レザミンCU−4550 75部 (大日精化工業株式会社製,エステル型ポリウレタン樹
脂) PAU−3 25部 (三菱化成株式会社製,ポリアミノ酸ウレタン樹脂) レザミンX 1部 (大日精化工業株式会社製,イソシアネート化合物) N・N−ジメチルホルムアミド 25部 マグネシア100B 5部 (宇部化学工業株式会社製,平均粒径10〜20nmの
MgO微粉末)Formulation 2 Resamine CU-4550 75 parts (Dainichi Seika Kogyo Co., Ltd., ester type polyurethane resin) PAU-3 25 parts (Mitsubishi Kasei Co., Ltd., polyamino acid urethane resin) Resamine X 1 part (Dainichi Seika) Industrial Co., Ltd., isocyanate compound) N · N-dimethylformamide 25 parts Magnesia 100B 5 parts (Ube Chemical Co., Ltd., average particle size 10-20 nm MgO fine powder)
【0035】本発明との比較のため,本実施例において
処方2からマグネシア100Bを除くほかは,本実施例
と全く同一の方法により比較用のコーテイング布帛(比
較例3とする)を得た。For comparison with the present invention, a comparative coating fabric (referred to as Comparative Example 3) was obtained in the same manner as in this Example except that Magnesia 100B was omitted from Formulation 2 in this Example.
【0036】本発明および比較例3のコーテイング布帛
の性能を測定,評価し,その結果を合わせて表2に示し
た。The performances of the coating fabrics of the present invention and Comparative Example 3 were measured and evaluated, and the results are shown in Table 2 together.
【0037】[0037]
【表2】 [Table 2]
【0038】表2に示す結果から明らかなように,本発
明のコーテイング布帛は,優れた耐水圧と透湿度を有す
るとともに,高透湿性防水布帛の欠点である漏水性に対
しても有効であり,かつ耐摩耗性,耐剥離性も良好であ
ることがわかる。As is clear from the results shown in Table 2, the coating fabric of the present invention has excellent water pressure resistance and moisture permeability and is also effective against water leakage, which is a drawback of the highly moisture permeable waterproof fabric. It is also found that the wear resistance and peeling resistance are also good.
【0039】[0039]
【発明の効果】本発明方法によれば,優れた透湿性能お
よび防水性能を有するコーテイング布帛を得ることがで
きる。さらに,本発明のコーテイング布帛は,コーテイ
ング樹脂層の耐摩耗性,耐剥離性にも優れている。本発
明によれば,湿式コーテイングのみで透湿性,防水性の
いずれにおいても高性能が得られるので,コストも安く
製造することができ,産業上非常に有利である。本発明
のコーテイング布帛は,その優れた性能から,特に雨
衣,外衣等の衣料に適した素材である。According to the method of the present invention, it is possible to obtain a coated cloth having excellent moisture permeability and waterproof performance. Further, the coating fabric of the present invention is excellent in abrasion resistance and peeling resistance of the coating resin layer. According to the present invention, since high performance can be obtained in terms of both moisture permeability and waterproofness only by wet coating, it can be manufactured at low cost, which is very advantageous in industry. The coating fabric of the present invention is a material suitable for apparel such as rain clothes and outer garments because of its excellent performance.
Claims (2)
成重合体からなる有孔の樹脂層を有し,該樹脂層中に実
質的に無孔で平均粒径が0.1μm以下の無機微粉末を1
%以上含有し,6000g/m2・24hrs以上の透湿度
と0.6kg/cm2 以上の耐水圧を有することを特徴とする
透湿性能および防水性能の優れたコーテイング布帛。1. An inorganic fine powder having a porous resin layer made of a synthetic polymer mainly composed of polyurethane resin on a fiber cloth, the resin layer being substantially non-porous and having an average particle size of 0.1 μm or less. 1
%, More than 6000 g / m 2 · 24 hrs moisture permeability and 0.6 kg / cm 2 or more water pressure resistant coating fabric with excellent moisture permeability and waterproof performance.
1μm以下の無機微粉末を樹脂固形分に対して1%以上
含むポリウレタン樹脂主体の合成重合体溶液を塗布し,
しかる後に水中に浸漬して樹脂分の湿式凝固を行うこと
を特徴とする透湿性能および防水性能の優れたコーテイ
ング布帛の製造方法。2. A fiber cloth having substantially no pores and an average particle size of 0.
Apply a synthetic polymer solution mainly composed of polyurethane resin containing 1% or more of inorganic fine powder of 1 μm or less with respect to resin solid content,
A method for producing a coating fabric having excellent moisture permeability and waterproofing properties, which comprises immersing the resin component in water for wet coagulation.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20131091A JP2951442B2 (en) | 1991-07-15 | 1991-07-15 | Coating fabric and method for producing the same |
| US07/909,157 US5204403A (en) | 1991-07-15 | 1992-07-06 | Moisture permeable and waterproof coated fabric and method for manufacturing same |
| EP19920202146 EP0523806B1 (en) | 1991-07-15 | 1992-07-14 | Moisture permeable and waterproof coated fabric and method for manufacturing same |
| DE69210698T DE69210698T2 (en) | 1991-07-15 | 1992-07-14 | Moisture-permeable, water-impermeable, coated textile fabric and method for its production |
| HK98101353A HK1002320A1 (en) | 1991-07-15 | 1998-02-23 | Moisture permeable and waterproof coated fabric and method for manufacturing same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20131091A JP2951442B2 (en) | 1991-07-15 | 1991-07-15 | Coating fabric and method for producing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05222677A true JPH05222677A (en) | 1993-08-31 |
| JP2951442B2 JP2951442B2 (en) | 1999-09-20 |
Family
ID=16438888
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20131091A Expired - Fee Related JP2951442B2 (en) | 1991-07-15 | 1991-07-15 | Coating fabric and method for producing the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2951442B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008307813A (en) * | 2007-06-15 | 2008-12-25 | Komatsu Seiren Co Ltd | Moisture permeable waterproof fabric and manufacturing method thereof |
-
1991
- 1991-07-15 JP JP20131091A patent/JP2951442B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008307813A (en) * | 2007-06-15 | 2008-12-25 | Komatsu Seiren Co Ltd | Moisture permeable waterproof fabric and manufacturing method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2951442B2 (en) | 1999-09-20 |
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