JPH0397970A - Waterproofing coating cloth having humidity-absorbing and releasing property - Google Patents
Waterproofing coating cloth having humidity-absorbing and releasing propertyInfo
- Publication number
- JPH0397970A JPH0397970A JP23052889A JP23052889A JPH0397970A JP H0397970 A JPH0397970 A JP H0397970A JP 23052889 A JP23052889 A JP 23052889A JP 23052889 A JP23052889 A JP 23052889A JP H0397970 A JPH0397970 A JP H0397970A
- Authority
- JP
- Japan
- Prior art keywords
- water
- property
- fabric
- absorbing
- moisture permeability
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 59
- 230000003578 releasing effect Effects 0.000 title claims abstract 5
- 239000011248 coating agent Substances 0.000 title abstract description 13
- 238000000576 coating method Methods 0.000 title abstract description 13
- 238000004078 waterproofing Methods 0.000 title abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 74
- 229920005749 polyurethane resin Polymers 0.000 claims abstract description 22
- 238000010521 absorption reaction Methods 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 14
- 230000035699 permeability Effects 0.000 claims abstract description 12
- 238000005406 washing Methods 0.000 claims abstract description 4
- 238000009833 condensation Methods 0.000 claims description 12
- 230000005494 condensation Effects 0.000 claims description 11
- 229920003002 synthetic resin Polymers 0.000 claims description 9
- 239000000057 synthetic resin Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 abstract description 17
- 239000011347 resin Substances 0.000 abstract description 17
- 239000000835 fiber Substances 0.000 abstract description 3
- 229920002635 polyurethane Polymers 0.000 abstract description 3
- 239000004814 polyurethane Substances 0.000 abstract description 3
- 239000011247 coating layer Substances 0.000 abstract description 2
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 230000000977 initiatory effect Effects 0.000 abstract 1
- 230000000704 physical effect Effects 0.000 abstract 1
- 239000005871 repellent Substances 0.000 description 21
- 230000002940 repellent Effects 0.000 description 21
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000011737 fluorine Substances 0.000 description 9
- 229910052731 fluorine Inorganic materials 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 239000010410 layer Substances 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000011342 resin composition Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- -1 polysiloxane Polymers 0.000 description 5
- 239000004677 Nylon Substances 0.000 description 4
- 239000012948 isocyanate 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
- 229920001778 nylon Polymers 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000005056 polyisocyanate Substances 0.000 description 3
- 229920001228 polyisocyanate Polymers 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000035900 sweating Effects 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- 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
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000034303 cell budding Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 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
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 150000005846 sugar alcohols Polymers 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
- 229940036248 turpentine Drugs 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
2.
1.
く産業上の利用分野〉
本発明は耐久性を有する結露防止性,帯電防止性.透湿
性,防水性および溌水性能を有する吸放湿性防水コーテ
ィング布帛に関する。[Detailed description of the invention] 2. 1. Industrial Application Fields> The present invention has durable anti-condensation and anti-static properties. This invention relates to a moisture absorbing and desorbing waterproof coated fabric that has moisture permeability, waterproofness, and water repellency.
く従来技術〉
従来より各種の防水性コーティング布帛が知られている
。例えば天然ゴム,合成ゴムあるいは合成樹脂などを被
覆した防水性コーティング生地がレインコート,ウイン
ドブレーカー等の防水衣料やテント,ターボリン,トラ
ック幌,積荷シート等に用いる防水シート類として製品
に実用化されている。Prior Art Various types of waterproof coated fabrics have been known. For example, waterproof coated fabrics coated with natural rubber, synthetic rubber, or synthetic resin have been put to practical use in products such as waterproof clothing such as raincoats and windbreakers, and waterproof sheets for use in tents, turbolins, truck hoods, cargo seats, etc. There is.
しかし防水衣料においては樹脂皮plA層の透湿性が低
く肴用時のムレによる不快感及び発汗で衣服内が高温多
湿になった場合、衣服内に水蒸気が凝結する現象(以下
結露と称す)が生じ、著しく着用感を悪くしていた。防
水衣料の内部多湿化による着用不快感の解決策としては
、例えば通気性を強調した高密度織物に溌水処理を施し
た布帛があるが、その耐水圧は使用した生地の組織,密
度および繊度により決定されるが、せいぜい200〜3
00履口20程度の不充分なものであり、かつ撥水耐久
性がないので一時的な防水性しかなく実用的な防水布帛
としては不適当であった。However, in waterproof clothing, the resin skin PLA layer has low moisture permeability, and when the inside of the clothing becomes hot and humid due to discomfort due to stuffiness during serving or sweating, water vapor condenses inside the clothing (hereinafter referred to as condensation). This caused the wearer to noticeably deteriorate the feeling of wearing. As a solution to the discomfort of wearing waterproof clothing due to high internal humidity, for example, there is a high-density fabric that emphasizes breathability and is treated with water repellent treatment, but its water resistance depends on the structure, density, and fineness of the fabric used. It is determined by, but at most 200 to 3
The fabric had an insufficient water repellency of about 20 mm and had no water repellent durability, so it had only temporary waterproof properties and was unsuitable as a practical waterproof fabric.
一方特公昭60−47954号公報,特公昭60−47
955月公報および特開昭63−182475号公報等
には、ポリウレタン重合体を主体とした合或樹脂皮膜層
から構成される微多孔質皮膜がその表面に多数の微細な
小孔をもち皮膜内部にも連通した空洞部を持ち微細小孔
の直径が5μ以下であって透湿度が80009/m・2
4時間以下の様な′S湿性,防水性布帛が開示されてい
るが、かかる布帛では発汗時の水蒸気の凝結を防止する
には不充分であり、防水布帛でありながら衣服内は雨で
濡れた様な状態となる。On the other hand, Japanese Patent Publication No. 60-47954, Publication No. 60-47
955 and Japanese Patent Application Laid-Open No. 182475/1984, etc., a microporous film composed of a synthetic resin film layer mainly composed of polyurethane polymer has many fine pores on its surface and the interior of the film is It has a cavity that communicates with the air, the diameter of the micropores is 5μ or less, and the moisture permeability is 80009/m・2.
Although a fabric is disclosed that has a moisture resistance of 4 hours or less and is waterproof, such fabric is insufficient to prevent condensation of water vapor during sweating, and even though it is a waterproof fabric, the inside of the garment may get wet due to rain. It will be in a similar state.
更に防水性を高める為に撥水処理が施ざれているが、こ
れではコーティング布帛全体が疎水性となるので静電気
の発生が強く薯用時のまとわりつきゃ放電時の電気ショ
ックなどで着用時の不快感が増大する。Furthermore, water repellent treatment is applied to improve waterproofness, but since the entire coated fabric is hydrophobic, it generates strong static electricity, causing damage when worn due to clinging when used or electric shock during discharging. Pleasure increases.
一方衣服内の水蒸気の充満を防ぐ為に合成樹脂皮膜の小
孔の直径を更に大きく皮膜層内部との連通方式にした場
合は防水性の低下,合或樹脂皮膜層の強度低下を引きお
こし、摩耗による皮膜破れが生じ着用耐久性の悪いもの
となる。On the other hand, if the diameter of the small pores in the synthetic resin film is made larger and communicated with the inside of the film layer in order to prevent water vapor from filling inside the clothes, this will cause a decrease in waterproofness and/or a decrease in the strength of the resin film layer. The film will break due to abrasion, resulting in poor wearing durability.
一方防水シート類としては、綿等の天然繊維から或る織
物にバラフィン,金属石鹸等により防水処理を施したも
のが用いられていた。On the other hand, waterproof sheets have been made of natural fibers such as cotton, which have been waterproofed with paraffin, metal soap, and the like.
これらはその織目間隙が防水剤により完全にはふさがれ
ていない為、この織目間隙を空気や湿気が通過して内部
にムレや結露を生じることがないという利点を右してい
た。しかし天然繊雑の強度が比較的低く十分に強いシー
トを得るにはかなりの厚地としなければならず、この結
果重程が大どなるという欠点があった。この為に近年は
強度が高くしかも軒昂である合成!INシートが多用さ
れるようになって来た。しかし合成繊維シートの場合、
疎水性でかつ水膨潤性に欠けるので、従来の綿シート等
が吸水すると次第にi潤し結果的に漏水を防止し得ると
いう長所があったのに対し、合戒繊維にはこの長所が用
持し得す従って全く水を通さないシートを得る為には基
布表面に合成樹脂での皮g層を形成せしめざるを得ない
。しかし、この場合、合或IM防水シートを使ってテン
トあるいは幌等を構成すると結露現象が生じる。These have the advantage that because the interwoven gaps are not completely blocked by the waterproofing agent, air and moisture will not pass through the interwoven gaps and cause stuffiness or condensation inside. However, the strength of natural fibers is relatively low, and in order to obtain a sufficiently strong sheet, it must be made quite thick, which has the disadvantage of increasing the weight. For this reason, in recent years, synthetic materials with high strength and eaves! IN sheets have come into widespread use. However, in the case of synthetic fiber sheets,
Because it is hydrophobic and lacks water-swellability, conventional cotton sheets have the advantage that when they absorb water, they gradually become wet and can prevent water leakage. Therefore, in order to obtain a sheet that does not allow water to pass through at all, it is necessary to form a skin layer of synthetic resin on the surface of the base fabric. However, in this case, if a tent or a canopy is constructed using a composite IM tarpaulin sheet, dew condensation occurs.
この解決策として特開昭56−37370号公報に示さ
れている如クlI雑性訪水布に親水性物質を被覆するこ
とが挙げられるが、当該品は合或樹脂又はゴム等で被覆
されている防水布であるため透湿度がゼロ又はゼロに近
い値であり、布帛内部に充満した水蒸気を放出すること
が難しい。また親水性物質が水分を吸収したあと水分の
樹脂皮vA層への拡散は行われるが湿度の低い外部への
結露水の蒸発はゴム又は合威樹脂皮膜層にさえぎられて
出来ない。従ってこれを解決するためには親水性物質が
結露水を吸収する能力すなわち吸水倍率の高い樹脂を利
用する必要がある。As a solution to this problem, coating a hydrophilic substance on a miscellaneous water-receiving fabric as shown in JP-A No. 56-37370 can be mentioned, but this product is coated with a synthetic resin or rubber, etc. Because it is a waterproof fabric, its moisture permeability is zero or close to zero, making it difficult to release the water vapor that fills the fabric. Further, after the hydrophilic substance absorbs water, the water diffuses into the resin coating vA layer, but the evaporation of condensed water to the outside where humidity is low is blocked by the rubber or synthetic resin coating layer. Therefore, in order to solve this problem, it is necessary to use a hydrophilic substance that has the ability to absorb condensed water, that is, a resin that has a high water absorption capacity.
しかし吸水倍率の大きい樹脂の場合(1)体積膨張する
力の方が基布又は合成樹脂と接着している力より強くな
り剥離を起す、(2吸水した水分を放出する時間すなわ
ち可逆時間が長くなり繰り返し使用に支障をきたす等の
欠点が生ずる。However, in the case of resins with high water absorption capacity, (1) the force of volumetric expansion is stronger than the force of adhesion to the base fabric or synthetic resin, causing peeling; (2) the time to release absorbed water, that is, the reversible time is long; This results in drawbacks such as difficulty in repeated use.
〈発明の目的〉
本発明は上述の諸欠点を解消した優れた結露防止性能,
透湿性,帯電防止性および防水性を有するコーティング
布帛を提供するものである。<Object of the invention> The present invention eliminates the above-mentioned drawbacks and provides excellent dew condensation prevention performance.
The present invention provides a coated fabric that has moisture permeability, antistatic properties, and waterproof properties.
〈発明の構或〉
上記目的を達成するための本発明の構成は以下の通りで
ある。<Structure of the Invention> The structure of the present invention for achieving the above object is as follows.
1. 繊維性基布の少なくとも片面にポリウレタン系樹
脂を主体とする合成樹脂皮膜を有するコーティング布帛
であって、コーティング面の結露開始時間が50分以上
、摩擦帯電圧が500V以下、透湿性が2000〜80
00g/cm2・24時間、耐水圧が500〜3000
s口20であって,J I 3 1−1042−83
G法に準する洗濯回数45回後も前記性能の80%
以上を保持することを特徴とする吸放湿性防水コーティ
ング布帛。1. A coated fabric having a synthetic resin film mainly composed of polyurethane resin on at least one side of a fibrous base fabric, with a dew condensation onset time on the coated surface of 50 minutes or more, a frictional charging voltage of 500 V or less, and a moisture permeability of 2000 to 80.
00g/cm2・24 hours, water pressure resistance 500-3000
s port 20, J I 3 1-1042-83
80% of the above performance even after 45 washes according to G method
A moisture-absorbing and desorbing waterproof coated fabric characterized by retaining the following properties.
2. ポリウレタン系樹脂の吸水性能が自重の0.5〜
50倍、最大吸水時の体積膨張が50倍以下、放湿性能
が30分以下である請求項(1)に記載の吸放湿性防水
コーティング布帛。2. The water absorption performance of polyurethane resin is 0.5 to its own weight.
The moisture absorbing and desorbing waterproof coated fabric according to claim 1, which has a volumetric expansion of 50 times or less at maximum water absorption, and a moisture release performance of 30 minutes or less.
ここに繊維性基材とは、特に限定はなく合成繊維,天然
yam等のいかなるものであっても良く、また織物,編
物.不織布などすべての組織のものが使用される。又こ
れらのmN布帛に予め撥水剤処理を施したものを用いる
。この場合、布帛の旧水性能はJIS L−1096
スプレー法にて撥水度80以上であることが望ましい。The fibrous base material herein is not particularly limited and may be any material such as synthetic fibers, natural yam, etc., and may also include woven fabrics, knitted fabrics, etc. All types of fabrics, including non-woven fabrics, can be used. Moreover, these mN fabrics are used which have been previously treated with a water repellent. In this case, the old water performance of the fabric is JIS L-1096.
It is desirable that the water repellency is 80 or higher when measured by spraying.
用いる溌水剤はバラフィン系撥水剤.ボリシロキサン系
撥水剤あるいはフッ素系撥水剤等公知のものでよくその
処理は一般に行われている公知の方法で行ったものでよ
い。ただし本発明の特徴の一つである諸性能の高耐久性
に匹敵する撥水性の耐久性を得るにはフッ素系撥水剤と
メラミン樹脂併用およびフッ素系魔水剤の二段処理を行
うのが望ましい。例えば下記の配合された溌水剤浴にバ
デイング後120℃で1分間乾燥し150℃で1分間の
熱処理を行う。The water repellent used is a paraffin water repellent. A known water repellent such as a polysiloxane water repellent or a fluorine water repellent may be used, and the treatment may be carried out by a commonly known method. However, in order to obtain the durability of water repellency comparable to the high durability of various performances, which is one of the features of the present invention, it is necessary to perform two-step treatment using a combination of a fluorine-based water repellent and melamine resin and a fluorine-based water magic agent. is desirable. For example, after budding in a water repellent bath containing the following formulation, drying is performed at 120°C for 1 minute, and heat treatment is performed at 150°C for 1 minute.
アサヒガードL S −317 (旭硝子■〉 7%
スミテックスレジンM〜3(住友化学工業■)0.5%
スミテックスアクセレーターACX (同上)0.3%
またフッ素系撥水剤の二段処理方法の例としてはエマル
ジ3ン系のフッ素系撥水剤アサヒガードA G −71
0 (旭硝子QM製)5%溶液にて公知の方法にて処理
したあと溶剤系フッ素系撥水剤アサヒガードA G −
610 (旭硝子viJ製)5〜7%溶液にて公知の方
法にて処理を行えばよい。この場合溶剤系順水剤の処理
はポリウレタン樹脂のコーティング処理後に行う場合も
ある。Asahi Guard LS-317 (Asahi Glass ■) 7%
Sumitex Resin M~3 (Sumitomo Chemical ■) 0.5% Sumitex Accelerator ACX (same as above) 0.3% Also, examples of the two-step treatment method for fluorine-based water repellents include Emulsion 3-based fluorine-based Water repellent Asahi Guard A G-71
0 (manufactured by Asahi Glass QM) After treatment with a 5% solution using a known method, the solvent-based fluorine-based water repellent Asahi Guard A G -
610 (manufactured by Asahi Glass viJ) 5 to 7% solution may be used in a known manner. In this case, the treatment with the solvent-based water conditioner may be carried out after the coating treatment with the polyurethane resin.
本発明で用いるポリウレタン系樹脂の持つべき基本的特
性は(1)吸水性能が自重の0.5〜50イ8、(2)
放湿性能が30分以下4(3)吸水時の体積膨張が50
倍以下を兼ね備えることが必要である。The basic characteristics that the polyurethane resin used in the present invention should have are (1) water absorption performance of 0.5 to 50 of its own weight (2)
Moisture release performance is 30 minutes or less 4 (3) Volume expansion when absorbing water is 50
It is necessary to have at least double the amount.
すなわち結露した水分を吸収するための皮膜特性として
、吸水性能が0.5倍以下であれば結露した水分を充分
吸収出来ない。一方50倍以上と吸水能力が大きい場合
は、皮膜の吸水能力一杯まで吸水を続け放湿が始まらな
い為に体積膨張が大きくなりコーティングした樹脂皮膜
が布帛より剥離し実用に供し得ない。That is, as for the film characteristics for absorbing condensed moisture, if the water absorption performance is 0.5 times or less, the condensed moisture cannot be sufficiently absorbed. On the other hand, if the water absorption capacity is 50 times or more, water absorption continues until the water absorption capacity of the coating is reached and moisture release does not begin, resulting in increased volumetric expansion and the coated resin coating peels off from the fabric, making it impossible to put it to practical use.
一方放湿性能とは吸収した水分が水蒸気として蒸発し吸
水する前の状態にまで戻る性能を言うがこの現象には二
つの要因がある。On the other hand, moisture release performance refers to the ability of absorbed moisture to evaporate as water vapor and return to the state before water absorption, and there are two factors behind this phenomenon.
すなわち吸水した水分の樹脂皮膜内部への拡敗及び皮膜
界面からの水分の蒸発である。この放渇速度が30分以
内であることが必要である。That is, the absorbed water spreads into the resin film and the water evaporates from the film interface. It is necessary that this depletion rate be within 30 minutes.
上記速度が遅く、結露水が多量の場合は吸水能力を超え
てしまい結露防止効果が認められない。If the above speed is slow and there is a large amount of condensed water, the water absorption capacity will be exceeded and no dew condensation prevention effect will be observed.
また包含した水分のために樹脂皮膜の体積が膨張するが
、膨張率が50倍を超えると皮膜/基材の接着力よりも
膨張する力の方が大きい為、樹脂皮膜が基材より剥離す
る現象を引き起すか基拐面への力一リング現象が生ずる
。又前述の如き性能を有している樹脂皮膜層である為に
常時水分の吸収/放湿を繰り返しており、樹脂皮膜が水
分を保持した状態になる為に樹脂皮膜をコーティングさ
れた布帛はD電気防止性能を兼ね尚える。更に当該樹脂
皮膜は無孔質皮膜である為に皮膜の厚さにもよるが50
0〜5000am口20の防水性能を持っている。In addition, the volume of the resin film expands due to the contained moisture, but if the expansion rate exceeds 50 times, the expansion force is greater than the adhesive force between the film and the base material, causing the resin film to separate from the base material. This causes a force-ring phenomenon on the base surface. In addition, since the resin film layer has the above-mentioned performance, it constantly absorbs and releases moisture, and because the resin film retains moisture, the fabric coated with the resin film is D. It also has electric prevention performance. Furthermore, since the resin film is a non-porous film, it depends on the thickness of the film.
It has a waterproof performance of 0 to 5000 am.
前述の如き特性をもったポリウレタン系樹脂はポリイソ
シアネートとボリオールとを反応せしめて得られる重合
物であり、ポリイソシアネートとしては、公知の脂肪族
並びに芳香族ポリイソシアネートが使用でき、例えば,
ヘキサメチレンジイソシアネー]・,トルエンジイソシ
アネート.キシレンジイソシアネートおよびこれらの過
剰又は多価アルコールの過剰との反応生或物があげられ
る。A polyurethane resin having the above-mentioned properties is a polymer obtained by reacting a polyisocyanate with a polyol. As the polyisocyanate, known aliphatic and aromatic polyisocyanates can be used, for example,
Hexamethylene diisocyanate], toluene diisocyanate. Mention may be made of xylene diisocyanates and their reaction products with excesses or with excesses of polyhydric alcohols.
ボリオールとしては、ポリエーテルあるいはポリエステ
ル等、通常のポリウレタン樹脂製造に使用される公知の
ものが使用可能である。ボリエスブルとしては、例えば
、エチレングリコール.ジエチレングリコールまたは1
,4−ブタンジオール等の多価アルコールとアジビン酸
,フタル酸またはセパチン酸等の多塩基性カルボン酸と
の反応物があげられる。ポリエーテルとしては、例えば
、エチレングリコールにエチレンオキシド,ブロビレン
オキシド,ブヂレンオキシド等のアルキレンオキシドの
1種また2種以上を付加させたものがあげられる。更に
、樹脂皮膜と布帛との耐剥離性を向上させる目的で、樹
脂溶液にlI+H基布との親和性の高い化合物を併用す
る。本発明では、その化合物としてイソシアネート化合
物を併用する。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,イソフオロンジインシアネート,ヘキサ
メチレンジ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され
る。As the polyol, known polyols such as polyether or polyester, which are used in the production of ordinary polyurethane resins, can be used. For example, ethylene glycol. diethylene glycol or 1
, 4-butanediol, and a polybasic carboxylic acid such as adivic acid, phthalic acid, or sepatic acid. Examples of the polyether include those obtained by adding one or more alkylene oxides such as ethylene oxide, brobylene oxide, and butylene oxide to ethylene glycol. Furthermore, for the purpose of improving the peeling resistance between the resin film and the fabric, a compound having high affinity with the lI+H base fabric is used in combination with the resin solution. In the present invention, an isocyanate compound is also used as the compound. As an isocyanate compound, 2.4
- Tolylene diisocyanate. Triisocyanates obtained by an addition reaction between 3 moles of diphenylmethane diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, or these diisocyanates and 1 mole of a compound containing active hydrogen (for example, trimethylolpropane, glycerin, etc.) used.
上述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、あるいはフェノール.メチルエ
チルケトオキシム等を付加することにより安定させ、そ
の後の熱処理によりブロッ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。イソシアネート化合物の使用量と
しては、ポリウレタン系樹脂の総重量に対して0.1〜
10%、好ましくは0.5〜5%の割合で使用すること
が望ましい。使用はが0.1%未満であれば、布帛に対
する樹脂の接着力が乏しく、逆に10%を超えると、風
合が硬化するので好ましくない。The above-mentioned isocyanates may be those in which the isocyanate group is free or phenol. Even if it is stabilized by adding methyl ethyl ketoxime or the like and the blocks are dissociated by subsequent heat treatment, any type can be used, and it may be used appropriately depending on workability, purpose, etc. The amount of isocyanate compound used is 0.1 to 0.1 to the total weight of the polyurethane resin.
It is desirable to use it in a proportion of 10%, preferably 0.5-5%. If the amount is less than 0.1%, the adhesion of the resin to the fabric will be poor, and if it exceeds 10%, the texture will be hardened, which is not preferable.
上述のポリウレタン系樹脂の!l維性基材へのコーティ
ング方法は公知の方法にて実施すればよい。Of the polyurethane resin mentioned above! The method for coating the fibrous base material may be carried out by a known method.
く実浦例〉
次に実施例にまり本介明をさらに具体的に説明するが本
実施例におけるコーティング布帛の性能の測定,評価は
次の方法によって行った。Kumiura Example> Next, the present invention will be explained in more detail with reference to an example. The performance of the coated fabric in this example was measured and evaluated by the following method.
(1)結露開始時間:外気温O℃,水温25℃の境界に
コーティグ面を高温側にし
て試料を設置しコーティング
面に水滴が凝結し始める時間。(1) Condensation start time: The time when water droplets begin to condense on the coated surface when a sample is placed with the coated surface on the high temperature side at the boundary between the outside temperature of 0°C and the water temperature of 25°C.
(2)!!擦帯電圧(V):JIS L−1094−
80B法 20℃.40%R }−1
(till定条件〉
0)透湿性:JIS Z−0208
i4) 耐水圧:JTS L−1079(9 溌水
性:JIS L−1092(6)洗濯耐久性:JIS
L−1042−83 G法実施例1
ポリエステルタフタ(経, l#75deのポリエステ
ルフィラメント糸,たて密度×よこ密度が各々110本
/インチ,90本/インチ)を公知の方法にて精練,ブ
リセット,染色を施した。次いで下記の処方のフッ素系
溌水剤での溌水処理を行い旧水度100の布帛を得た。(2)! ! Friction voltage (V): JIS L-1094-
80B method 20℃. 40%R}-1 (till constant conditions) 0) Moisture permeability: JIS Z-0208 i4) Water pressure resistance: JTS L-1079 (9) Water repellency: JIS L-1092 (6) Washing durability: JIS
L-1042-83 G method Example 1 Polyester taffeta (warp, l#75de polyester filament yarn, warp density x width density of 110 threads/inch and 90 threads/inch, respectively) was scoured and blistered by a known method. Set and dyed. Next, water repellent treatment was performed using a fluorine-based water repellent having the following formulation to obtain a fabric with a water content of 100.
〈撥水処理処方〉
アサヒガードL S −317 (旭硝子■〉7.0%
スミテツクスレジンM−3(住友化学工業■)0.5%
スミテックスアクセレータ−ACX (同上)063%
下記に示したポリウレタン系樹脂溶液を当該布帛にナイ
フコーターを用いてコーティングを行い120℃で2分
乾燥、150℃で1分間の熱処理を行った。塗工された
ポリウレタン系樹脂は10g/ 771であった。<Water repellent treatment prescription> Asahi Guard LS-317 (Asahi Glass ■) 7.0%
Sumitex Resin M-3 (Sumitomo Chemical ■) 0.5% Sumitex Accelerator-ACX (same as above) 063% Coat the fabric with the polyurethane resin solution shown below using a knife coater and heat at 120°C. It was dried for 2 minutes and heat treated at 150°C for 1 minute. The amount of coated polyurethane resin was 10g/771.
〈コーティング処方〉
ラックスキンU Z −264 (セイコー化成■)1
00部
メチルエチルケトン(MEK) 15部得られ
た布帛は表■に示した通りの特性をもっていた。<Coating prescription> Luxkin U Z -264 (Seiko Kasei ■) 1
00 parts Methyl ethyl ketone (MEK) 15 parts The obtained fabric had the properties shown in Table 3.
実施例2
ナイロンタフタ(経,緯70deナイロンフィラメント
糸、たて密度×よこ密度120本/インチ×86本/イ
ンチ)を公知の方法にて精練.染色を施した。次いで実
施例1と同様の条件にて溌水処理を施し、撥水度100
の布帛を得た。更に下記に示したポリウレタン系樹脂溶
液にて湿潤での塗工全18g/Tdになる様ナイフコー
ターにてコーティングを行った。次いで実施例1と同様
の熱処理を行った。更に撥水性の耐洗濯性向上の為に下
記の処方にてフッ素系溌水剤によるバディングを行い1
20℃,2分の乾燥、150℃.1分の熱処理を実施し
表■に示した特性をもった]一ティング布帛を得た。Example 2 Nylon taffeta (warp and weft 70 de nylon filament yarn, warp density x width density 120 threads/inch x 86 threads/inch) was refined by a known method. Stained. Next, water repellency treatment was performed under the same conditions as in Example 1, resulting in a water repellency of 100.
fabric was obtained. Furthermore, coating was performed using a knife coater using the polyurethane resin solution shown below so that the total wet coating amount was 18 g/Td. Then, the same heat treatment as in Example 1 was performed. Furthermore, in order to improve water repellency and wash resistance, we applied padding with a fluorine-based water repellent using the following formulation.
Drying at 20°C for 2 minutes, 150°C. A heat treatment was carried out for 1 minute to obtain a fabric having the properties shown in Table (3).
〈ポリウレタン系樹脂組戊〉
ラックスキンLJ Z −264 (セイコー化成■製
)100部
ダイラックホワイトl −1500(大日本インキ化学
■製) 10部メチルエ
チルケトン(MFK) 20部〈フッ素系撥水
剤組成〉
アサヒガードA G −610 (旭硝子■製〉ミネラ
ルターペン
7部
100部
実施例3
ナイロンタック(経70de,緯85deのナイロンフ
ィラメント糸、たて×よこの密度は各々 165本/イ
ンヂ×97本/インチ)を公知の方法にて染色した。次
いで実施例1と同様の溌水処理を施し坦水度100の布
帛を得た。次に下記に示すポリウレタン系樹脂溶液にて
塗工1209/mになる様にナイフコーターでコーティ
ングを行った。次いで120’CX2分の乾燥を行い実
施例2と同様の溌水処理を行い表王に示した特性をもっ
たコーティング布帛を4.1だ。<Polyurethane resin composition> Luxkin LJ Z -264 (manufactured by Seiko Kasei ■) 100 parts Dylac White L -1500 (manufactured by Dainippon Ink Chemical ■) 10 parts Methyl ethyl ketone (MFK) 20 parts <Fluorine water repellent composition > Asahi Guard A G-610 (manufactured by Asahi Glass ■) Mineral turpentine 7 parts 100 parts Example 3 Nylon tack (nylon filament thread of warp 70 de, weft 85 de, density of warp x width each 165 pieces / inch x 97 pieces / inch) was dyed by a known method.Then, the same water repellency treatment as in Example 1 was carried out to obtain a fabric with a water repellency of 100.Next, it was coated with a polyurethane resin solution shown below at a rate of 1209/m. The fabric was coated with a knife coater so that the fabric was coated with a knife coater.Next, it was dried for 120'C x 2 minutes and subjected to the same water repellent treatment as in Example 2 to obtain a coated fabric with the properties shown in Table 4.1.
〈ポリウレタン系樹脂組成〉
フックスキンIJ Z −265 (セイコー化成■製
〉100部
グイラックホワイトl −1500(大日本インキ化
学@J製) 10部
ダイラックブラック5179 (同上) 3部M
E K 20部
比較例1
実施例1と同様な布帛及び撥水処理を行った布帛を用い
下記に示したポリウレタン系樹脂溶液にてナイフコータ
ーを用いてコーティングを行い120℃で2分の乾燥、
150’Cで1分間の熱処理を行った。得られたコーテ
ィング布帛は表工に示した通りであった。<Polyurethane resin composition> Hookskin IJ Z -265 (manufactured by Seiko Kasei ■) 100 parts Guirac White L -1500 (manufactured by Dainippon Ink Chemical @ J) 10 parts Dylac Black 5179 (same as above) 3 parts M
EK 20 parts Comparative Example 1 Using the same fabric as in Example 1 and a fabric treated with water repellent treatment, coat with the polyurethane resin solution shown below using a knife coater, dry at 120°C for 2 minutes,
Heat treatment was performed at 150'C for 1 minute. The obtained coated fabric was as shown in the front surface.
〈ポリウレタン系樹脂溶液組成〉
クリスボン2116−E L (大日本イキン化学■製
100部ク
リスボン NX(大日本インキ化学■製〉3部
トルエン 20部比較
例2
実!lIA2においてポリウレタン系m脂溶液を下記に
示した樹脂組成とし湿潤時の塗工量を30g/dにした
以外は同様の方法にてコーティング布帛を得た。得られ
た布帛の特性は表Iに示した通りであり、透湿性,防水
性および撥水性能は有しているが結露性能及びυ1電性
能は有していなかった。<Polyurethane resin solution composition> Crysbon 2116-EL (manufactured by Dainippon Ink Chemical ■) 100 parts Crisbon NX (manufactured by Dainippon Ink Chemical ■) 3 parts toluene 20 parts Comparative Example 2 A polyurethane resin solution was prepared as follows in IA2. A coated fabric was obtained in the same manner except that the resin composition was changed to 30 g/d when wet.The properties of the obtained fabric were as shown in Table I, including moisture permeability, Although it had waterproofness and water repellency, it did not have dew condensation performance or υ1 electric performance.
くポリウレタン系樹脂組成〉
XOLTEX PX IOOF(大日本化学工業■製
)100部
ダイラツクホワイトL−5513 ( I1)
10部XOLTEX CL−10 (〃)
3fllM E K
20部トルエン
10部水
4011
比較例3
実施例3においてポリウレタン系溶液を下記に示した樹
脂組成とし湿潤状態での塗工出を30g/dとした以外
は同様の方法にてコーティング布帛を{qだ。得られた
布帛の特性は表工に示した通りであり、比較例2と同様
、結露性および訓電性能を有していなかった。Polyurethane resin composition>
10 parts XOLTEX CL-10 (〃)
3fllM E K
20 parts toluene
10 parts water 4011 Comparative Example 3 A coated fabric was prepared in the same manner as in Example 3 except that the polyurethane solution had the resin composition shown below and the coating output in a wet state was 30 g/d. The properties of the obtained fabric were as shown in the surface finish, and like Comparative Example 2, it did not have dew condensation or electrical training performance.
くボリウタレン系樹脂組成〉
クリスボンN¥T−20(大日本インキ化学工業■)
100部イソフタル
酸(IPA) 7部トルエン
7部比較例4
比較例1と同様の方法にてコーティング及び乾燥したコ
ーティング布帛に更に実施@1と同様の方法でポリウレ
タン系樹脂をコーティング.乾燥及び熱処理を実施しコ
ーティング布帛を{qた。得られた布帛の特性は表Iの
通りであった。Kubouriuthalene resin composition> Crisbon N¥T-20 (Dainippon Ink & Chemicals ■)
100 parts isophthalic acid (IPA) 7 parts toluene
7 parts Comparative Example 4 The coated fabric coated and dried in the same manner as in Comparative Example 1 was further coated with polyurethane resin in the same manner as in Example 1. Drying and heat treatment were performed to obtain the coated fabric. The properties of the obtained fabric were as shown in Table I.
Claims (1)
を主体とする合成樹脂皮膜を有するコーティング布帛で
あって、コーティング面の結露開始時間が50分以上、
摩擦帯電圧が500V以下、透湿性が2000〜800
0g/cm^2・24時間、耐水圧が500〜3000
mmH_2Oであつて、JISL−1042−83G法
に準する洗濯回数45回後も前記性能の80%以上を保
持することを特徴とする吸放湿性防水コーティング布帛
。 2、ポリウレタン系樹脂の吸水性能が自重の0.5〜5
0倍、最大吸水時の体積膨張が50倍以下、放湿性能が
30分以下である請求項(1)に記載の吸放湿性防水コ
ーティング布帛。[Scope of Claims] 1. A coated fabric having a synthetic resin film mainly composed of polyurethane resin on at least one side of a fibrous base fabric, wherein the onset time of dew condensation on the coated surface is 50 minutes or more;
Frictional charging voltage is 500V or less, moisture permeability is 2000-800
0g/cm^2・24 hours, water pressure resistance 500-3000
mmH_2O, and retains 80% or more of the above-mentioned performance even after washing 45 times according to the JISL-1042-83G method. 2. The water absorption performance of polyurethane resin is 0.5 to 5 of its own weight.
The moisture absorbing and releasing waterproof coated fabric according to claim 1, which has a volumetric expansion of 0 times and maximum water absorption of 50 times or less, and a moisture release performance of 30 minutes or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23052889A JPH0397970A (en) | 1989-09-07 | 1989-09-07 | Waterproofing coating cloth having humidity-absorbing and releasing property |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23052889A JPH0397970A (en) | 1989-09-07 | 1989-09-07 | Waterproofing coating cloth having humidity-absorbing and releasing property |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0397970A true JPH0397970A (en) | 1991-04-23 |
Family
ID=16909162
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23052889A Pending JPH0397970A (en) | 1989-09-07 | 1989-09-07 | Waterproofing coating cloth having humidity-absorbing and releasing property |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0397970A (en) |
Cited By (5)
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WO1998058107A3 (en) * | 1997-06-13 | 1999-03-18 | Texel Inc | Method for constructing wind resistant canvas covers |
US6046119A (en) * | 1998-01-28 | 2000-04-04 | Toyo Boseki Kabushiki Kaisha | Heat-retaining, moisture-permeable, waterproof fabrics |
EP1260355A1 (en) * | 2000-09-29 | 2002-11-27 | Toray Industries, Inc. | Warmth retaining fiber structure |
JP2018043244A (en) * | 2017-12-22 | 2018-03-22 | 日東電工株式会社 | Moisture permeable filter medium |
CN112791602A (en) * | 2021-01-27 | 2021-05-14 | 泉州师范学院(石狮)生态智能织物工程技术研究院 | Bamboo raw powder/polyurethane composite membrane and preparation method and application thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS619423A (en) * | 1984-06-22 | 1986-01-17 | Toyo Tire & Rubber Co Ltd | Polyurethane polymer |
JPS6356212B2 (en) * | 1982-03-01 | 1988-11-07 | Kuraray Co |
-
1989
- 1989-09-07 JP JP23052889A patent/JPH0397970A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6356212B2 (en) * | 1982-03-01 | 1988-11-07 | Kuraray Co | |
JPS619423A (en) * | 1984-06-22 | 1986-01-17 | Toyo Tire & Rubber Co Ltd | Polyurethane polymer |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998058107A3 (en) * | 1997-06-13 | 1999-03-18 | Texel Inc | Method for constructing wind resistant canvas covers |
US6046119A (en) * | 1998-01-28 | 2000-04-04 | Toyo Boseki Kabushiki Kaisha | Heat-retaining, moisture-permeable, waterproof fabrics |
EP1260355A1 (en) * | 2000-09-29 | 2002-11-27 | Toray Industries, Inc. | Warmth retaining fiber structure |
EP1260355A4 (en) * | 2000-09-29 | 2007-07-11 | Toray Industries | Warmth retaining fiber structure |
JP2018043244A (en) * | 2017-12-22 | 2018-03-22 | 日東電工株式会社 | Moisture permeable filter medium |
CN112791602A (en) * | 2021-01-27 | 2021-05-14 | 泉州师范学院(石狮)生态智能织物工程技术研究院 | Bamboo raw powder/polyurethane composite membrane and preparation method and application thereof |
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