JPS6143193B2 - - Google Patents
Info
- Publication number
- JPS6143193B2 JPS6143193B2 JP20001481A JP20001481A JPS6143193B2 JP S6143193 B2 JPS6143193 B2 JP S6143193B2 JP 20001481 A JP20001481 A JP 20001481A JP 20001481 A JP20001481 A JP 20001481A JP S6143193 B2 JPS6143193 B2 JP S6143193B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- absorbing
- layer
- hygroscopic
- sheet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000463 material Substances 0.000 claims description 57
- 239000010410 layer Substances 0.000 claims description 38
- 239000011358 absorbing material Substances 0.000 claims description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 239000002250 absorbent Substances 0.000 claims description 23
- 239000002344 surface layer Substances 0.000 claims description 19
- 230000002745 absorbent Effects 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000004745 nonwoven fabric Substances 0.000 description 21
- 238000010521 absorption reaction Methods 0.000 description 15
- 239000003973 paint Substances 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 13
- 238000000034 method Methods 0.000 description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000004793 Polystyrene Substances 0.000 description 8
- 238000009833 condensation Methods 0.000 description 8
- 239000000123 paper Substances 0.000 description 8
- 229920002223 polystyrene Polymers 0.000 description 8
- 230000005494 condensation Effects 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000011810 insulating material Substances 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 239000012298 atmosphere Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 229920001400 block copolymer Polymers 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- 239000012790 adhesive layer Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920001084 poly(chloroprene) Polymers 0.000 description 3
- 229920002857 polybutadiene Polymers 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 229920000800 acrylic rubber Polymers 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000005034 decoration Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 238000009423 ventilation Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- CWMYWRMDANXCSB-UHFFFAOYSA-N 1-oxoethanesulfonic acid Chemical compound CC(=O)S(O)(=O)=O CWMYWRMDANXCSB-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical class [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000007791 dehumidification Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- OAMZXMDZZWGPMH-UHFFFAOYSA-N ethyl acetate;toluene Chemical compound CCOC(C)=O.CC1=CC=CC=C1 OAMZXMDZZWGPMH-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229920001600 hydrophobic polymer Polymers 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Building Environments (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Laminated Bodies (AREA)
Description
本発明は吸水性または吸湿性シート材料の製造
方法に関し、特に住宅その他湿気の発生し易い場
所の結露防止材として有用な吸水性または吸湿性
シート材料の提供を目的とする。
最近の住宅は、集合化、高層化の傾向があると
ともに、それらの建材として、コンクリート、鉄
骨、ガラス等の無吸湿性の材料が多く使用され、
またサツシ、ドアー等が使用されて住居が密閉化
され、更に各種の暖房が普及した結果、室内の壁
面、床面面、天井面における結露現象が多発し、
壁材の剥離、カビの発生、畳の損傷、家具の汚染
等の被害が多発するようになつた。
上記の如き結露防止の方法としては、断熱材を
使用する断熱方式、換気・除湿方式、呼吸性結露
防止塗膜方式等が知られているが、断熱方式では
非常に厚い断熱層が必要であり、費用、スペー
ス、工法の面で十分な効果を得ることができず、
換気方式は最も良い方法であるが、暖房効果と相
反するので現実には不可能であり、除湿機は一般
家庭向きではない。また、結露防止塗料を用いる
方式では、形成した塗膜の吸湿量が低く、且つ吸
湿した状態ではその表面が膨潤した状態になり、
その上に各種の内装を施すことが困難であり、内
装を施した場合は、その内装材が剥離する場合が
多い。
本発明者は、上記の如き従来技術の欠点を解決
すべく鋭意研究の結果、高湿度の雰囲気では1m2
あたり約100〜3000gという多量の水分を吸湿で
き、しかもその表面は吸湿した状態でも乾燥状態
であり、且つ雰囲気が乾燥時にはその吸湿した水
分を徐々に放湿するという、いわゆる呼吸性のあ
る吸水性・吸湿性シートを開発し、上述の従来技
術の欠点を解決することができた。
すなわち、本発明は、通気性を有するシート状
基材の片面に吸水性材料を含む液状組成物を塗布
して、その基材の表面層を残してその基材中に吸
水性材料を含浸させ、次いでその塗布面に吸水性
材料が実質的に存在しない裏面層を形成せしめる
ことからなる吸水性・吸湿性シート材料の製造方
法である。
本発明を、本発明の実施例を説明する添附図面
を参照して詳細に説明する。
第1図は本発明の吸水性・吸湿性シート材料の
典型的で好ましい例を示すものであり、1は本発
明の吸水性・吸湿性シート材料を、2は必要に応
じて設けてもよい接着剤層、3は必要に応じて設
けてもよい断熱材や離型紙であり、4は吸水性材
料が実質的に存在しない裏面層であり、5は吸水
性材料からなる吸水性・吸湿性層であり、6は吸
水性材料が実質的に存在しない通気性表面層であ
る。この実施態様では、1で示したシート材料の
基材は約0.1〜5mmの厚さの合成繊維からなる不
織布であり、この不織布1の一方の面に、吸水性
材料の微粉末を、単独であるいは任意のバインダ
ーとともに水や有機媒体中に分散あるいは溶解さ
せた液状材料(塗料)を塗布し、不織布の他の面
の一部6を残すように含浸せしめて、吸水性・吸
湿性の層5を形成せしめ、次いで上記塗料の塗布
面に通気性のないプラスチツクシート、不織等の
通気性シートを貼着したり、あるいは合成樹脂塗
料や通気性層を形成し得るポリウレタン塗料等を
塗布して吸水性材料が実質的に存在しない裏面層
4を形成する。この裏面層4は接着剤層2を兼ね
たものでもよい。更に必要に応じて断熱材や離型
紙3を設けてもよい。この実施態様では吸水性材
料からなる塗料を不織布1の全体に含浸させず
に、その表面に通気性の層6を残すことが重要で
ある。このような構成は、吸水性材料からなる塗
料を、使用する不織布の性質に応じて、その粘
度、吸水性材料の濃度等を調整し、吸水性材料の
含浸速度をコントロールすることにより容易に実
現することができる。また、通気性表面6を形成
すべき部分に予め溶剤可溶性の物質を充填してお
き、吸水性材料からなる塗料を不織布に十分に含
浸させ、乾燥した後に、その充填物質を溶出除去
することにより形成させても通気性表面層6を形
成することができる。通気性表面層6にまで吸水
性材料が存在すると、シート材料1の表面を常に
乾燥状態に保持することが困難で、従つてシート
材料1の表面に各種の加工を施すことが困難にな
る。また、裏面層に実質的な量の吸水性材料が存
在すると、表面層と同様に各種の装飾加工が困難
であつたり、まだ壁面等との接着等が困難とな
る。
第2図は本発明の吸水性・吸湿性シート材料の
別の実施態様を示すものである。このシート材料
1は、吸水性・吸湿性層5を別に用意し、次いで
その両面を加工するものである。すなわち、不織
布等の基材5に吸水性材料からなる塗料を全体的
に含浸させ、次いで、その両面に湿式のポリウレ
タンやアクリル系樹脂塗料により通気性の層を形
成し、その一方を表面層6とし他方を裏面層4と
する。また、吸水・吸湿性層5の一方の面にプラ
スチツクシートやフイルムまたは合成樹脂塗料等
を適用して裏面層4を形成し、次いで他の面に不
織布等の通気性材料を積層したり、あるいは上記
と同様な通気性層6を形成することによつて本発
明の吸水性・吸湿性シート1を形成する。また、
両面とも不織布等の通気性材料を積層して表面層
6および裏面層4を形成してもよく、この場合に
重要なことは表面層6と吸水性・吸湿性層5との
接着界面を通気性に保持することであり、接着剤
による点接着や糸による縫合等、従来公知の手段
により容易に実現することができる。
以上、本発明の典型的な実施態様を例示した
が、本発明はこのような例示に限定されず、各種
の変形や修正した実施態様が可能であり、且つそ
のような態様も包含するものである。
本発明で使用する基材としては、不織布の他、
紙、織布、合成樹脂発泡体、フエルト、綿、ウエ
ブ、スポンジ、グラス布、その他の通気性材料が
いずれも使用でき、それらの好ましい厚さは約
0.1〜15mm程度である。
本発明で使用する吸水性材料としては、(1)特開
昭54−47796、83091、83989、87791号公報その他
に開示される如き、本発明者による、親水性基を
有するポリマーあるいはコポリマーに疎水性のポ
リマー鎖あるいはコポリマー鎖がブロツクコポリ
マーまたはグラフトコポリマーの形で結合した吸
水性樹脂、(2)澱粉−ポリアクリル酸ソーダグラフ
ト化物、澱粉−ポリアクリロニトリルグラフト化
物のケン化物、セルロース−ポリアクリル酸ソー
ダグラフト化物、ビニルアルコール−アクリル酸
ソーダ共重合物、ビニルアルコール−メタクリル
酸ソーダ共重合物、ポリアクリル酸ソーダ、カル
ボキシメチルセルローズのソーダ塩、ポリエチレ
ンオキサイド等の如く、水溶性樹脂を物理的ある
いは化学的に架橋させて吸水性としたもの等の如
き吸水性高分子、吸水性樹脂、水膨潤性高分子、
水膨潤性樹脂等がいずれも使用することができ、
またそれ以外の各種の固体の乾燥剤も使用するこ
とができるが、好ましいものは、多量の水分(例
えば自重の数十倍から数百倍)を吸収してもその
水分によつて溶解しない吸水性高分子材料〔前記
(1)および(2)〕が好ましいものである。このような
吸水性材料は本発明においては、各種の有機溶
剤、例えばトルエン、キシレン、シクロヘキサ
ン、メチルエチルケトン、酢酸エチル、ジオキサ
ン、テトラヒドロフラン、ジメチルホルムアミ
ド、メタノール、エタノール、ブタノールあるい
はそれらの混合物中に約1〜50重量%の割合で微
分散せしめ、好ましくは更にクロロプレンゴム、
アクリルゴム、ウレタンゴム、ブチラール樹脂、
エチレン−酢酸ビニル共重合体、スチレンブタジ
エン共重合体、ブタジエン合成ゴム、ニトリルゴ
ム、イソブレンゴム、ポリスチレン−ポリブタジ
エン−ポリスチレンブロツクコポリマー、ポリス
チレン−ポリイソプレン−ポリスチレンブロツク
コポリマー等のバインダー成分を吸水性材料100
重量部あたり約5〜60重量部の割合で存在せしめ
て、粘度が約10〜10000センチポイズの液状の組
成物として使用するのが好ましい。更に必要に応
じて、可塑剤、防かび剤、難燃剤、香料、紫外線
吸収剤、着色剤、脱臭剤等を添加してもよい。こ
のような液状組成物は、刷毛、ヘラ、バーコータ
ー、ハンドローラー、スプレー、ロールコータ
ー、フローコーター、デイツプコーター等の従来
公知の手段によつて不織布等の基材に塗布あるい
は含浸せしめることができる。塗布あるいは含浸
せしめる量は使用する基材の種類、厚さ、用途、
吸水性材料の種類、吸水率その他の条件によつて
変化し一概には決められないが、用途が結露防止
用シートである場合は、得られる吸水性シート材
料の吸水量が約100〜1500g水分/m2となる量で
ある。特開昭54−47796号公報に記載の吸水性材
料を使用するときは、不織布1m2あたり約10〜
100gの吸水性材料を吸水性・吸湿性層中に包含
させるのが好ましい。また、吸水性材料が実質的
に存在しない表面層の厚さが約1〜100ミクロン
程度になる様に含浸させるのが好ましい。
本発明における吸水性材料が実質的に存在しな
い裏面層の形成に使用する材料は、その形成方法
により異なるが、塗料型組成物を塗布して形成す
る場合は、前記のバインダー成分の外に、塩ビ酢
ビ共重合体、アクリル系共重合体、湿式ウレタン
用ウレタン樹脂、ポリエステル樹脂、酢酸ビニル
樹脂等の高分子材料を前記の如き任意の有機溶剤
に溶解し、これを任意の塗布手段によつて塗布
し、乾燥し、約1ミクロン程度以上の通気性ある
いは通気性のない被膜を形成することにより形成
することができる。た、無溶剤型のホツトメルト
型接着剤や感熱型の接着剤を塗布して裏面層を形
成し、更に離型紙や比較的薄い断熱材と積層する
こともできる。
以上の如くして得られた本発明の吸水性・吸湿
性シート材料は、通気性表面層、吸水性・吸湿性
層および裏面層からなる構成で、その通気性の表
面層と裏面層は実質的に吸水性材料を含有しな
い。
従つて、このようなシート材料は高湿度雰囲気
(例えば、冬期の暖房した室内の押入れの北側壁
面やタタミの裏側等)において、本来結露すべき
多量の水分を吸収保持することができ、且つ吸湿
した状態でもその表面層と裏面積は乾燥した状態
に保持されているから、その表面に設けられてい
る壁紙その他の内装材を剥離したり汚染すること
がない。また本発明の吸水性・吸湿性シートの裏
面層も常に乾燥状態にあるから、吸湿された水分
が壁面とシートの接着を害することもない。
以上の通り、本発明の吸水性シートは住宅の結
露防止材として非常に有用であるとともに、その
他ペツトの下敷、靴の中敷、地表、地中の水分除
去、植物用鉢の保水および放湿による湿度調整等
吸湿性や吸水性が要求される用途に有用である。
次に実施例をあげて本発明を具体的に説明す
る。なお、文中、部または%とあるのは重量基準
である。
実施例 1
(ポリスチレン)−(ポリブタジエン〓ポリスチ
レン)(ポリスチレン含有量30%)で表わされる
テレキーリツク型ブロツクコポリマーのポリブタ
ジエンに当量のチオグリコール酸を付加させ、次
いでナトリウム塩にした吸水性ポリマー(吸水度
60)16部を62部のメチルエチルケトンに分解させ
た分散液と、20部の20%クロロプレンゴムトルエ
ン溶液とを混合して塗料を得る。この塗料を、坪
量100g/m2、厚さ0.4mmのポリエステル不織布の
一方の面に200g/m2の割合でバーコーターにより
塗布した。塗料は不織布の厚さの約0.3mmまで滲
透したが、裏面までは達しなかつた。次いで80℃
で20分間乾燥した。次いで、20%クロロプレンゴ
ムトルエン溶液を上記の含浸不織布の同一面に
125g/m2の割合でバーコーターにより塗布し、80
℃で20分間乾燥させて裏面層を形成し、本発明の
吸水性・吸湿性シート材料を得た。このシート材
料の表面層は厚さ約0.12mmであり、吸水性・吸湿
性層の厚さは約0.25mmであり、裏面層の厚さは約
30ミクロンであつた。この吸水性・吸湿性シート
材料を相対湿度100%、温度差約60℃の雰囲気に
4時間放置したところ約700g/m2の吸湿量を示
し、その後相対湿度50%(20℃)の室内に放置し
たところ、約6時間でその全量を放湿した。この
操作を10回繰返してもその吸湿量に変化は認めら
れず。またシートの表面状態にも変化は認められ
なかつた。また、冬期に結露により寝具が濡れる
という状態の高層住宅の押入れの床面に敷いてお
いたところ、それらの寝具の濡れは全く発生しな
くなつた。
実施例 2
実施例1の吸水性・吸湿性シート材料の裏面層
に厚さ4mmの独立発泡型ポリエチレン断熱シート
を接着剤により貼着し、本発明の別の吸水性・吸
湿性シートを得た。このシートの実施例1と同一
条件での吸湿量は500g/m2(4時間後)であり、
6時間後に700g/m2を示し、発泡体の断熱効果を
示した。このシートについて、吸湿および放湿を
10回繰返しても、シートと断熱材の接着力の低下
は認められなかつた。
実施例 3
実施例1で使用した吸水性ポリマーの分散液50
部と67部の15%アクリルゴムトルエン−酢酸エチ
ル溶液とを混合して塗料を得、坪量120g/m2、厚
さ0.5mmのナイロン製不織布の片面から上記の塗
料を200g/m2の割合で含浸させる。この場合の含
浸は不織布の厚さの50%であつた。乾燥後、上記
の含浸面に15%アクリルゴムトルエン−酢酸エチ
ル溶液を134g/m2の割合で塗布し、実施例1と同
様に乾燥して本発明の吸水性・吸湿性シート材料
を得た。このシートの表面層の厚さは約0.23mmで
あり、吸水性・吸湿性層の厚さは約0.25mmであ
り、且つ裏面層の厚さは約20ミクロンであつた。
この吸水性・吸湿性シートを相対湿度100%、温
度差60℃の雰囲気におくと約4時間で約200g/m2
の吸湿量を示し、相対湿度50%(20℃)の室内に
放置したところ約2時間で全量を放湿した。この
シート材料の表面層に化粧紙を貼着した後、相対
湿度100%、温度差60℃の雰囲気に2時間放置し
てもその化粧紙の剥離は生じなかつた。
実施例 5
実施例1で得られた吸水性・吸湿性シート材料
2枚を裏面同志で熱圧着したものは、最大吸水量
が1500g/m2に達し、その乾燥時の放湿も速やか
であつた。このシートを裁断してゴム長靴の中敷
を作成し使用してみたところ、非常にすぐれた吸
湿性を示し、足のムレが殆んど感じられず、使用
後、放置することにより繰返し使用が可能であつ
た。
実施例 6
実施例1において、不織布に吸水性ポリマーお
よび裏面層を付与する前に、不織布の片面にポリ
酢酸ビニルのメタノール溶液(約1000ポイズ)を
約4g/m2(固形分)の割合で塗布し乾燥後、そ
の反対面において実施例1の操作を繰返し、最後
にメタノール中に一日浸漬し、ポリ酢酸ビニルを
溶解除去して通気性の表面層を再生し、本発明の
吸水性・吸湿性シート状材料を得た。このシート
材料の性質は実施例1のものと同様であつた。
実施例 7〜10
(ポリスチレン〓ポリブタジエン〓ポリスチレ
ン)(ポリスチレン含有量40%)のテレキーリツ
ク型ブロツクコポリマーにアセチルスルホン酸を
反応させ、ナトリウム塩にした吸水性ポリマー
(吸水度80)(実施例7)、ポリアクリル酸ナトリ
ウム系吸水性ポリマー(吸水度100)(実施例
8)、架橋アクリル酸メチル−酢酸ビニルコポリ
マーをケン化して得られる吸水性ポリマー(吸水
度120)(実施例9)およびデンプンにアクリル酸
ナトリウムをグラフトした吸水性ポリマー(吸水
度150)(実施例10)を使用し、他は実施例1と同
様にして得た本発明の吸水性・吸湿性シート材料
の性能は下記第1表の通りであつた。
なお、以上の実施例における「吸水度」とは、
吸水性ポリマー1gが吸水保持し得る水の量
(g)を表わしている。
The present invention relates to a method for producing a water-absorbing or hygroscopic sheet material, and particularly aims to provide a water-absorbing or hygroscopic sheet material useful as a dew condensation prevention material for houses and other places where moisture is likely to occur. In recent years, housing has tended to become clustered and high-rise, and many non-hygroscopic materials such as concrete, steel frames, and glass are used as building materials.
In addition, as a result of the use of sashes, doors, etc., which made homes hermetically sealed, and the spread of various types of heating, condensation frequently occurred on indoor walls, floors, and ceilings.
Damages such as peeling of wall materials, growth of mold, damage to tatami mats, and contamination of furniture have become frequent. As methods for preventing dew condensation as described above, there are known methods such as heat insulation methods using heat insulating materials, ventilation/dehumidification methods, and breathable dew condensation prevention coating methods, but the heat insulation methods require a very thick insulation layer. , it was not possible to obtain sufficient effects in terms of cost, space, and construction methods.
Ventilation is the best method, but it is actually impossible because it conflicts with the heating effect, and dehumidifiers are not suitable for general households. In addition, in the method using anti-condensation paint, the amount of moisture absorbed by the formed coating film is low, and when it absorbs moisture, its surface becomes swollen.
It is difficult to apply various types of interior decoration on it, and when interior decoration is applied, the interior material often peels off. As a result of intensive research to solve the above-mentioned drawbacks of the conventional technology, the inventor of the present invention found that
It can absorb a large amount of moisture (approximately 100 to 3000 g per unit), and its surface remains dry even when it absorbs moisture, and when the atmosphere is dry, it gradually releases the absorbed moisture, so-called breathable water absorption.・We developed a hygroscopic sheet and were able to solve the above-mentioned drawbacks of the conventional technology. That is, the present invention involves applying a liquid composition containing a water-absorbing material to one side of a sheet-like base material having air permeability, and impregnating the water-absorbing material into the base material while leaving a surface layer of the base material. This is a method for producing a water-absorbent/hygroscopic sheet material, which comprises forming a back layer substantially free of water-absorbing material on the coated surface. The invention will now be described in detail with reference to the accompanying drawings, which illustrate embodiments of the invention. FIG. 1 shows a typical and preferred example of the water-absorbent/hygroscopic sheet material of the present invention, where 1 indicates the water-absorbent/hygroscopic sheet material of the present invention, and 2 may be provided as necessary. Adhesive layer 3 is a heat insulating material or release paper that may be provided as necessary, 4 is a back layer substantially free of water-absorbing material, and 5 is a water-absorbing/hygroscopic layer made of a water-absorbing material. 6 is a breathable surface layer substantially free of water-absorbing material. In this embodiment, the base material of the sheet material indicated by 1 is a nonwoven fabric made of synthetic fibers with a thickness of about 0.1 to 5 mm, and one surface of this nonwoven fabric 1 is coated with fine powder of a water-absorbing material. Alternatively, a liquid material (paint) dispersed or dissolved in water or an organic medium is applied together with an arbitrary binder, and impregnated so as to leave part 6 of the other surface of the nonwoven fabric, thereby forming a water-absorbing/hygroscopic layer 5. Then, a non-porous plastic sheet, a non-woven or other breathable sheet is attached to the surface coated with the above paint, or a synthetic resin paint or a polyurethane paint that can form a breathable layer is applied. A back layer 4 substantially free of water-absorbing material is formed. This back layer 4 may also serve as the adhesive layer 2. Furthermore, a heat insulating material or release paper 3 may be provided as necessary. In this embodiment, it is important to leave the breathable layer 6 on the surface of the nonwoven fabric 1 without impregnating the entire surface of the nonwoven fabric 1 with a paint made of a water-absorbing material. Such a structure can be easily achieved by adjusting the viscosity of the paint made of water-absorbing material, the concentration of the water-absorbing material, etc. according to the properties of the nonwoven fabric used, and controlling the impregnation rate of the water-absorbing material. can do. Alternatively, the portion where the breathable surface 6 is to be formed is filled with a solvent-soluble substance in advance, the nonwoven fabric is sufficiently impregnated with a paint made of a water-absorbing material, and after drying, the filling substance is eluted and removed. Even if it is formed, the air permeable surface layer 6 can be formed. If the water-absorbing material is present even in the air-permeable surface layer 6, it will be difficult to keep the surface of the sheet material 1 dry at all times, and therefore it will be difficult to perform various treatments on the surface of the sheet material 1. Furthermore, if a substantial amount of water-absorbing material is present in the back layer, it will be difficult to perform various decorative treatments as with the front layer, and it will also be difficult to adhere to walls and the like. FIG. 2 shows another embodiment of the water-absorbent/hygroscopic sheet material of the present invention. This sheet material
In No. 1 , a water-absorbent/hygroscopic layer 5 is prepared separately, and then both surfaces thereof are processed. That is, a base material 5 such as a nonwoven fabric is entirely impregnated with a paint made of a water-absorbing material, and then a breathable layer is formed on both sides using wet polyurethane or acrylic resin paint, and one side is covered with a surface layer 6. The other layer is used as the back layer 4. Alternatively, the back layer 4 may be formed by applying a plastic sheet, film, synthetic resin paint, etc. to one side of the water/hygroscopic layer 5, and then a breathable material such as non-woven fabric may be laminated to the other side, or The water absorbent/hygroscopic sheet 1 of the present invention is formed by forming the same breathable layer 6 as described above. Also,
The surface layer 6 and the back layer 4 may be formed by laminating breathable materials such as non-woven fabrics on both sides. In this case, it is important that the adhesive interface between the surface layer 6 and the water-absorbent/hygroscopic layer 5 be ventilated. This can be easily achieved by conventionally known means such as spot bonding with adhesive or suturing with thread. Although typical embodiments of the present invention have been illustrated above, the present invention is not limited to these examples, and various modifications and modified embodiments are possible, and such embodiments are also included. be. In addition to nonwoven fabrics, base materials used in the present invention include
Paper, woven fabric, synthetic resin foam, felt, cotton, web, sponge, glass cloth, and other breathable materials can all be used, with a preferred thickness of approx.
It is about 0.1 to 15 mm. The water-absorbing material used in the present invention includes (1) a hydrophobic polymer or copolymer having a hydrophilic group, as disclosed in JP-A-54-47796, 83091, 83989, 87791 and others; (2) starch-sodium polyacrylate grafted product, saponified starch-polyacrylonitrile grafted product, cellulose-sodium polyacrylate Water-soluble resins such as grafted products, vinyl alcohol-sodium acrylate copolymers, vinyl alcohol-sodium methacrylate copolymers, sodium polyacrylate, carboxymethyl cellulose soda salt, polyethylene oxide, etc. water-absorbing polymers, water-absorbing resins, water-swellable polymers, such as those made water-absorbent by crosslinking with
Any water-swellable resin etc. can be used.
Various other solid desiccants can also be used, but preferred ones are water-absorbing agents that do not dissolve even if they absorb a large amount of moisture (for example, tens to hundreds of times their own weight). polymeric material [mentioned above]
(1) and (2)] are preferred. Such water-absorbing materials can be used in the present invention in various organic solvents such as toluene, xylene, cyclohexane, methyl ethyl ketone, ethyl acetate, dioxane, tetrahydrofuran, dimethylformamide, methanol, ethanol, butanol, or mixtures thereof. Finely dispersed in a proportion of 50% by weight, preferably further containing chloroprene rubber,
Acrylic rubber, urethane rubber, butyral resin,
Water-absorbing materials such as ethylene-vinyl acetate copolymer, styrene-butadiene copolymer, butadiene synthetic rubber, nitrile rubber, isobrene rubber, polystyrene-polybutadiene-polystyrene block copolymer, polystyrene-polyisoprene-polystyrene block copolymer, etc.
Preferably, it is present in a proportion of about 5 to 60 parts by weight and used as a liquid composition having a viscosity of about 10 to 10,000 centipoise. Furthermore, if necessary, plasticizers, fungicides, flame retardants, fragrances, ultraviolet absorbers, colorants, deodorizers, etc. may be added. Such a liquid composition can be applied or impregnated onto a substrate such as a nonwoven fabric by conventionally known means such as a brush, spatula, bar coater, hand roller, spray, roll coater, flow coater, dip coater, or the like. The amount to be applied or impregnated depends on the type and thickness of the substrate used, its purpose,
Although it cannot be definitively determined as it varies depending on the type of water-absorbent material, water absorption rate, and other conditions, if the application is a sheet for preventing condensation, the water absorption amount of the resulting water-absorbent sheet material is approximately 100 to 1,500 g of water. / m2 . When using the water-absorbing material described in JP-A-54-47796, approximately 10 ~
Preferably, 100 g of water-absorbing material is included in the water-absorbent layer. Further, it is preferable to impregnate the surface layer so that the thickness of the surface layer, which is substantially free of the water-absorbing material, is about 1 to 100 microns. The materials used to form the back layer substantially free of water-absorbing material in the present invention vary depending on the method of formation, but when forming by applying a paint-type composition, in addition to the binder component described above, A polymeric material such as a vinyl chloride-vinyl acetate copolymer, an acrylic copolymer, a urethane resin for wet urethane, a polyester resin, or a vinyl acetate resin is dissolved in any organic solvent as mentioned above, and this is applied by any coating method. It can be formed by applying the film and drying it to form an air permeable or non-air permeable film of about 1 micron or more. Alternatively, a back layer can be formed by applying a solvent-free hot melt adhesive or a heat-sensitive adhesive, and then laminated with release paper or a relatively thin heat insulating material. The water-absorbing/hygroscopic sheet material of the present invention obtained as described above has a structure consisting of an air-permeable surface layer, a water-absorbing/hygroscopic layer, and a back layer, and the air-permeable surface layer and back layer are substantially Contains no water-absorbing materials. Therefore, such sheet materials can absorb and retain a large amount of moisture that should normally condense in a high humidity atmosphere (for example, on the north wall of a closet in a heated room in winter or on the back side of a tatami mat). Since the surface layer and back surface are kept dry even when the surface is exposed, wallpaper and other interior materials provided on the surface will not peel off or become contaminated. Furthermore, since the back layer of the water-absorbent/hygroscopic sheet of the present invention is always in a dry state, absorbed moisture will not impair the adhesion between the sheet and the wall surface. As described above, the water-absorbing sheet of the present invention is very useful as a dew condensation prevention material for houses, as well as for use as an underlay for pets, insoles for shoes, for removing moisture from the ground surface and underground, and for water retention and moisture release in plant pots. It is useful for applications that require hygroscopicity or water absorption, such as humidity control. Next, the present invention will be specifically explained with reference to Examples. Note that parts and percentages in the text are based on weight. Example 1 An equivalent amount of thioglycolic acid was added to polybutadiene of a telechelic type block copolymer represented by (polystyrene)-(polybutadiene=polystyrene) (polystyrene content 30%), and then a water-absorbing polymer (water absorption
60) A paint is obtained by mixing a dispersion obtained by decomposing 16 parts into 62 parts of methyl ethyl ketone and 20 parts of a 20% chloroprene rubber toluene solution. This paint was applied at a rate of 200 g/m 2 to one side of a polyester nonwoven fabric having a basis weight of 100 g/m 2 and a thickness of 0.4 mm using a bar coater. The paint permeated through the nonwoven fabric to a thickness of approximately 0.3 mm, but did not reach the back side. Then 80℃
and dried for 20 minutes. Then, apply 20% chloroprene rubber toluene solution to the same side of the above impregnated nonwoven fabric.
Coated with a bar coater at a rate of 125g/ m2 ,
It was dried at ℃ for 20 minutes to form a back layer, thereby obtaining a water-absorbing and hygroscopic sheet material of the present invention. The surface layer of this sheet material is approximately 0.12 mm thick, the water-absorbent layer is approximately 0.25 mm thick, and the back layer is approximately 0.12 mm thick.
It was 30 microns thick. When this water-absorbing/hygroscopic sheet material was left in an atmosphere with a relative humidity of 100% and a temperature difference of about 60°C for 4 hours, it absorbed about 700 g/m 2 of moisture, and was then placed indoors at a relative humidity of 50% (20°C). When it was left to stand, the entire amount was released in about 6 hours. Even after repeating this operation 10 times, no change was observed in the amount of moisture absorbed. Further, no change was observed in the surface condition of the sheet. Furthermore, when the bedding was placed on the floor of a closet in a high-rise house where bedding gets wet due to condensation during the winter, the bedding no longer gets wet at all. Example 2 A 4 mm thick closed-cell polyethylene insulation sheet was adhered to the back layer of the water-absorbing/hygroscopic sheet material of Example 1 with an adhesive to obtain another water-absorbing/hygroscopic sheet of the present invention. . The moisture absorption amount of this sheet under the same conditions as Example 1 was 500 g/m 2 (after 4 hours),
It showed 700 g/m 2 after 6 hours, demonstrating the heat insulating effect of the foam. Regarding this sheet, moisture absorption and moisture release are
Even after repeating the test 10 times, no decrease in the adhesive strength between the sheet and the heat insulating material was observed. Example 3 Dispersion of water-absorbing polymer used in Example 1 50
200 g/m 2 of the above paint was mixed on one side of a nylon nonwoven fabric with a basis weight of 120 g/m 2 and a thickness of 0.5 mm. Impregnate in proportion. The impregnation in this case was 50% of the thickness of the nonwoven. After drying, a 15% acrylic rubber toluene-ethyl acetate solution was applied to the impregnated surface at a rate of 134 g/m 2 and dried in the same manner as in Example 1 to obtain a water-absorbent/hygroscopic sheet material of the present invention. . The thickness of the surface layer of this sheet was about 0.23 mm, the thickness of the water-absorbing/hygroscopic layer was about 0.25 mm, and the thickness of the back layer was about 20 microns.
When this water-absorbing/hygroscopic sheet is placed in an atmosphere with a relative humidity of 100% and a temperature difference of 60°C, it will absorb approximately 200 g/m 2 in approximately 4 hours.
When it was left in a room with a relative humidity of 50% (20°C), the entire amount of moisture was released in about 2 hours. After a decorative paper was attached to the surface layer of this sheet material, the decorative paper did not peel off even when it was left in an atmosphere with a relative humidity of 100% and a temperature difference of 60° C. for 2 hours. Example 5 The two sheets of the water-absorbing/hygroscopic sheet material obtained in Example 1 were bonded together on their backs by thermocompression, and the maximum water absorption amount reached 1500 g/ m2 , and the moisture released when drying was also rapid. Ta. When I cut this sheet to make insoles for rubber boots and used it, it showed very good moisture absorption, and my feet hardly felt stuffy. It was possible. Example 6 In Example 1, before applying the water-absorbing polymer and the back layer to the nonwoven fabric, a methanol solution of polyvinyl acetate (about 1000 poise) was applied to one side of the nonwoven fabric at a rate of about 4 g/m 2 (solid content). After coating and drying, the operation of Example 1 was repeated on the other side, and finally it was immersed in methanol for one day to dissolve and remove the polyvinyl acetate and regenerate the breathable surface layer. A hygroscopic sheet material was obtained. The properties of this sheet material were similar to those of Example 1. Examples 7 to 10 A water-absorbing polymer (water absorbency 80) made by reacting a telechelic type block copolymer of (polystyrene, polybutadiene, polystyrene) (polystyrene content: 40%) with acetylsulfonic acid to form a sodium salt (water absorption: 80), A water-absorbing polymer based on sodium polyacrylate (water absorption 100) (Example 8), a water-absorbing polymer obtained by saponifying a crosslinked methyl acrylate-vinyl acetate copolymer (water absorption 120) (Example 9), and starch with acrylic The performance of the water-absorbing/hygroscopic sheet material of the present invention obtained using a water-absorbing polymer grafted with sodium chloride (water absorbency 150) (Example 10) and in the same manner as in Example 1 is shown in Table 1 below. It was hot on the street. In addition, "water absorption" in the above examples is
It represents the amount of water (g) that 1 g of water-absorbing polymer can absorb and retain.
【表】
比較例 1
実施例1の方法において吸水性ポリマーを不織
布全体中に均一に含浸させた事を除いて他は実施
例1と同様に操作して得られた吸水性・吸湿性シ
ート材料の吸水量は約500g/m2であつたが、その
表面層に存在する吸水性ポリマーが吸水膨潤し凸
凹状の表面となり、摩擦により表面の吸水性ポリ
マーが脱落した。また、吸湿前にその表面に化粧
紙を貼着しておいたものは、その化粧紙が剥離し
た。
比較例 2
実施例1において、裏面層を形成しなかつたこ
とを除いて他は実施例1と同様に操作して得られ
た吸水性・吸湿性シート材料は約500g/m2の吸水
量を示すが、壁面に貼着した後に吸湿させるとそ
のシート材料は壁面から容易に剥離した。
実施例 11
比較例1において得られた吸水性・吸湿性シー
トの表面部分に厚さ0.1mmのポリエステル不織布
を縫合して本発明の吸水性・吸湿性シート材料を
得た。このシート材料の性能は実施例1のものと
同様であつた。
実施例 12
実施例1と同一の吸水性材料液を実施例1と同
様に不織布に塗布した後に、湿式用ウレタン樹脂
溶液(レザミンCV−520)(溶媒ジメチルホルム
アミド)を吸水性材料の塗布面にバーコーターで
塗布し、その後水中に浸漬して成膜し、イソプロ
ピルアルコールにて脱水し、乾燥し、本発明の吸
水性・吸湿性シート材料を得た。このものは防露
シート、調湿シートとして有用であつた。[Table] Comparative Example 1 A water-absorbent/hygroscopic sheet material obtained by the same procedure as in Example 1, except that the entire nonwoven fabric was uniformly impregnated with a water-absorbing polymer using the method of Example 1. The amount of water absorbed was about 500 g/m 2 , but the water-absorbing polymer present in the surface layer swelled with water and became an uneven surface, and the water-absorbing polymer on the surface fell off due to friction. In addition, when a decorative paper was attached to the surface before moisture absorption, the decorative paper peeled off. Comparative Example 2 A water-absorbing/hygroscopic sheet material obtained by performing the same procedure as in Example 1 except that the back layer was not formed had a water absorption amount of about 500 g/m 2 . As shown, the sheet material was easily peeled off from the wall surface when it was allowed to absorb moisture after being attached to the wall surface. Example 11 A polyester nonwoven fabric having a thickness of 0.1 mm was sewn onto the surface of the water absorbent/hygroscopic sheet obtained in Comparative Example 1 to obtain a water absorbent/hygroscopic sheet material of the present invention. The performance of this sheet material was similar to that of Example 1. Example 12 After applying the same water-absorbing material liquid as in Example 1 to a nonwoven fabric in the same manner as in Example 1, a wet urethane resin solution (Rezamin CV-520) (solvent dimethylformamide) was applied to the coated surface of the water-absorbing material. It was coated with a bar coater, then immersed in water to form a film, dehydrated with isopropyl alcohol, and dried to obtain a water-absorbent/hygroscopic sheet material of the present invention. This product was useful as a dew-proof sheet and a humidity control sheet.
第1〜2図は本発明の実施例を示すものであ
る。
1……吸水性・吸湿性シート材料、2……接着
剤層、3……断熱材、4……裏面層、5……吸水
性・吸湿性層、6……表面層。
1 and 2 show embodiments of the present invention. DESCRIPTION OF SYMBOLS 1... Water-absorbent/hygroscopic sheet material, 2... Adhesive layer, 3... Heat insulating material, 4... Back layer, 5... Water-absorbent/hygroscopic layer, 6... Surface layer.
Claims (1)
材料を含む液状組成物を塗布して、その基材の表
面層を残してその基材中に吸水性材料を含浸さ
せ、次いでその塗布面に吸水性材料が実質的に存
在しない裏面層を形成せしめることからなる吸水
性・吸湿性シート材料の製造方法。1. Apply a liquid composition containing a water absorbent material to one side of a breathable sheet-like base material, leave a surface layer of the base material and impregnate the water absorbent material into the base material, and then apply the water absorbent material to one side of the base material. 1. A method for producing a water-absorbing/hygroscopic sheet material, which comprises forming a back layer substantially free of water-absorbing material.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20001481A JPS58112727A (en) | 1981-12-14 | 1981-12-14 | Water-absorging and hygroscopic sheet material and its manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20001481A JPS58112727A (en) | 1981-12-14 | 1981-12-14 | Water-absorging and hygroscopic sheet material and its manufacture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58112727A JPS58112727A (en) | 1983-07-05 |
| JPS6143193B2 true JPS6143193B2 (en) | 1986-09-26 |
Family
ID=16417358
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20001481A Granted JPS58112727A (en) | 1981-12-14 | 1981-12-14 | Water-absorging and hygroscopic sheet material and its manufacture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58112727A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60110440A (en) * | 1983-11-21 | 1985-06-15 | 平岡織染株式会社 | Non-air-permeable hygroscopic and moisture-dissipating waterproof sheet |
| JPS6169305U (en) * | 1984-10-12 | 1986-05-12 |
-
1981
- 1981-12-14 JP JP20001481A patent/JPS58112727A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58112727A (en) | 1983-07-05 |
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