JPH0524273B2 - - Google Patents

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Publication number
JPH0524273B2
JPH0524273B2 JP58189023A JP18902383A JPH0524273B2 JP H0524273 B2 JPH0524273 B2 JP H0524273B2 JP 58189023 A JP58189023 A JP 58189023A JP 18902383 A JP18902383 A JP 18902383A JP H0524273 B2 JPH0524273 B2 JP H0524273B2
Authority
JP
Japan
Prior art keywords
vinyl
wall material
vinyl chloride
water
chloride resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP58189023A
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Japanese (ja)
Other versions
JPS6081378A (en
Inventor
Jiro Horikawa
Masato Ogura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP58189023A priority Critical patent/JPS6081378A/en
Publication of JPS6081378A publication Critical patent/JPS6081378A/en
Publication of JPH0524273B2 publication Critical patent/JPH0524273B2/ja
Granted legal-status Critical Current

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Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00Road transport of goods or passengers
    • Y02T10/10Internal combustion engine [ICE] based vehicles
    • Y02T10/12Improving ICE efficiencies

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  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
  • Laminated Bodies (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、結露防止用ビニル壁材に関する。さ
らに詳細には、壁紙や天井表装材などにおいて、
結露による水滴の発生を防止し、防かび性の向上
をはかつたシート状のビニル壁材に関する。 壁紙、天井表装材などの内装材としては、紙、
布、不織布などの基体に樹脂加工したものや、プ
ラスチツクシートそのものを加工したものなどが
多く用いられている。例えば、紙、布または不織
布に塩化ビニル樹脂を加工してなる壁材は、引つ
張り、引き裂きなどの強度が強く、また耐水性に
も優れ、汚れを容易に拭き落とせるなどの利点を
有することから、現在では居間などのほか、押入
れ、台所、トイレなどにも使用されている。しか
しこの壁材は、吸湿性に乏しいことから、室内と
室外との大きな温度差、あるいは室温の急変や湿
度の変化によつて、壁材の表面に水分が結露し、
水滴となつて現われるという欠点を有している。
このように水分が表面に結露すると、シミとして
残つたりかびがはえたりするといつた問題が生ず
る。また特に、住居の押入れの壁で結露すると、
ふとんなどが湿つて不快であり、不衛生となる。 このような紙、布または不織布に塩化ビニル樹
脂を加工してなる壁材の欠点を改良する手段とし
てはすでに、高吸水性高分子、塩化ビニル樹脂、
可塑剤および発泡剤からなるペーストゾルを、紙
などの基体に塗布したあと加熱することにより発
泡させた、いわゆる発泡紙が、高い吸水性と保水
性を有することから、この発泡紙を結露防止用壁
材として使用することが提案されている(特開昭
56−33032号公報)。 この公報に記載される壁材は、結露を防止する
効果は大きいものの、発泡層に吸収された水分の
一部が、裏打ちの基体や、壁材を貼り付けるため
に使用した糊材に移行するため、その部分の基体
が伸びて、きれいに貼つた壁材面にたるみやしわ
ができるとか、あるいは糊材にかびが生えたり糊
材が腐つたりしてその部分が劣化するといつた、
さらに改良すべき点を有していた。 本発明者らはこのような実情に鑑み、結露によ
る水滴の発生を防止しうる塩化ビニル壁材につい
てさらに鋭意検討を行つた結果、高吸水性高分子
を含有する塩化ビニル樹脂主体の発泡体層と基体
層との間に水不透過層を設けることにより、基体
の伸びに基づくしわや糊材におけるかびの発生が
なく、長期間使用しても、たるみの発生や壁素材
からの剥離が回壁できることを見出し、本発明を
完成するに至つた。 すなわち本発明は、塩化ビニル樹脂を主体とす
る合成樹脂、高吸水性高分子、可塑剤および任意
のその他の補助剤からなる樹脂組成物発泡体層
と、それを被覆する基体層とよりなるシートであ
つて、さらに発泡体層と基体層との間に水不透過
層を設けてなる結露防止用ビニル壁材を提供する
ものである。 本発明のビニル壁材は、外気と接する部分が高
吸水性高分子を含む樹脂発泡体であるので、壁が
それに接する空気の露点以下の温度になり、空気
中の水蒸気が凝縮水となるとき、その凝縮水をす
みやかに樹脂内部に吸収し、高吸水性高分子内に
保持する。したがつて結露が未然に防止される。
また樹脂層が発泡体なので、凝縮水を樹脂内部に
吸収するのが非常に早く、結露防止効果に優れて
いる。さらにこの壁材では、発泡体層と基体層と
の間に水不透過層を設けてあるため、吸収された
水分が基体まで浸透せず、水分による基体の伸び
や糊材の劣化も実質上起こさない。したがつて本
発明のビニル壁材は、それを壁面に貼つて使用し
た場合、きれいに貼つた状態が長期間保たれると
いう利点を有する。 ビニル壁材の樹脂組成物発泡体層に使用される
高吸水性高分子は、水を吸収して数倍から千数百
倍の重量に膨張し、保水はするが水には溶解しな
いものであれば、いかなるものでもよい。ただ、
吸水量が自重の30倍未満になると、結露した水分
を吸収させるために添加する高吸水性高分子が多
量に必要となり、ビニル壁材の引つ張り、引き裂
きなどの機械強度を低下させるので、使用する高
吸水性高分子の吸水量は、自重の30倍以上である
のが好ましい。高吸水性高分子の形状や粒子径に
ついても特に制限はないが、ビニル壁材の加工性
や物性などの面からみると、粒子径はできるだけ
細かいほうが望ましく、平均粒径が100μ以下、
さらには50μ以下のものがよい。 高吸水性高分子としては、公知の各種のもの、
例えば、澱粉とアクリロニトリルとのグラフト共
重合体のケン化物、澱粉とアクリル酸またはその
塩とのグラフト共重合体、スチレンと無水マレイ
ン酸との共重合体の塩、イソブチレンと無水マレ
イン酸との共重合体の塩を架橋させたもの、アク
リル酸および/またはアクリル酸塩の架橋重合体
(自己架橋型重合体、架橋剤共存下の重合による
架橋重合体、重合体の後架橋物など)、ポリビニ
ルアルコールと無水マレイン酸との反応物の塩、
ポリビニルアルコールとアクリル酸またはその塩
とのグラフト共重合体、ビニルエステルとエチレ
ン系不飽和カルボン酸またはその誘導体との共重
合体のケン化物、ビニルエステルと不飽和多価カ
ルボン酸またはその誘導体との共重合体のケン化
物、ポリビニルアルコール架橋体、ポリエチレン
グリコール架橋体、カルボキシメチルセルロース
架橋体、ポリビニルピロリドン架橋体、ポリアク
リルアミド架橋体、ポリアクリロニトリルのケン
化物、およびこれらの混合物などが使用しうる。 なかでも、架橋構造を有するカルボン酸およ
び/またはその塩を含む高分子電解質よりなる高
吸水性高分子は、吸水倍率が高く、かつ吸水後の
強度にも優れるので、こうしたものを用いるのが
好ましい。とりわけ、ビニルエステル(X)とエチレ
ン系不飽和カルボン酸またはその誘導体(Y)を主成
分とし、X:Y=10:90〜90:10なる範囲のモル
比で構成される共重合体のケン化物は、ことに吸
水後の強度が高く、吸水状態での耐候性および耐
熱性に優れ、これを使用した結露防止用壁材の結
露防止効果が長期間にわたつて持続するので、好
ましい。 高吸水性高分子の望ましい添加量は、塩化ビニ
ル樹脂100重量部に対して1重量部から200重量部
の範囲である。高吸水性高分子の量が1重量部未
満の場合には、吸湿性が小さくなつて結露現象を
充分に防止することができず、またその量が200
重量部を越えると、壁材としての強度が不充分と
なる。そのため、前記の範囲で高吸水性高分子を
使用するのが好ましいが、さらに好ましくは、塩
化ビニル樹脂100重量部に対して5重量部から150
重量部の範囲で用いられる。 本発明のビニル壁材において、樹脂組成物発泡
体層に使用さる塩化ビニル樹脂は、塩化ビニル重
合体、塩化ビニル共重合体、あるいはそれらの混
合物であつて、懸濁重合や乳化重合などの重合法
で得られる一般に使用されているものでよく、そ
の種類に特別な制限はない。さらには種々の改質
剤、、例えばPMMA,MBS,ABS,EVAなどの
他の樹脂を添加してもよい。 塩化ビニル樹脂に添加される可塑剤としては、
通常のものが用いられる。また難燃化のために
は、有機燐酸系の可塑剤を併用するのが望まし
い。 一般的な可塑剤の例としては、フタル酸ジオク
チル等のフタル酸エステル類、アジピン酸2−エ
チルヘキシル、セバチン酸ジオクチル等の二塩基
酸エステル類、エポキシ化大豆油、エポキシ化ア
マニ油、エポキシヘキサヒドロフタル酸ジオクチ
ル等のエポキシド類、ポリ(プロピレンアジペー
ト)、ポリ(1,3−ブチレンセバケート)、エチ
レンフタリルグリコール等の2価アルコールエス
テル類、塩素化パラフインなどが挙げられる。ま
た有機燐酸系可塑剤の例としては、燐酸トリクレ
ジル、燐酸クレジルフエニル、燐酸モノオクチル
ジフエニル、燐酸トリオクチル、燐酸トリフエニ
ル、燐酸トリブトキシエチル、燐酸トリブチルな
どが挙げられる。 可塑剤の望ましい使用量は、塩化ビニル樹脂
100重量部に対して30重量部から150重量部の範囲
であり、この範囲内で、目的に応じて任意の割合
をとることができる。 さらに、本発明のビニル壁材を構成する塩化ビ
ニル樹脂には、一般に使用される補助剤が必要に
応じて添加されてもよい。補助剤の添加割合は、
所望する製品により適宜変えることができる。こ
のような補助剤として具体的には、安定剤、炭酸
カルシウムやクレーのような無機充填剤、顔料、
希釈剤、難燃剤、防かび剤などが挙げられる。 本発明のビニル壁材を構成する樹脂組成物発泡
体は、一般に塩化ビニル樹脂発泡体を製造するた
めの公知のあらゆる方法によつて得られ、その製
造法に特別な制限はない。例えば、上記の原料を
配合したペースト状物に、気体または蒸気を吹き
込むとか、撹拌するとかにより、機械的に気泡を
存在させながら、ペーストを加熱してゲル化させ
る方法、上記原料に、加熱により分解して気体を
発生する発泡剤をあらかじめ添加混合しておき、
加熱ゲル化と同時に発泡させる方法、あるいは、
加熱ゲル化後、さらに高温で加熱して発泡させる
方法などによつて得られる。 なかでも発泡剤を使用する方法は、発泡セルが
細かく、その分布も均一であり、強度が大きくか
つ仕上がり外観の良好な発泡体が得られるので、
本発明のビニル壁材を構成する樹脂組成物発泡体
を得る方法として好ましい。使用しうる発泡剤と
しては、アゾジカルボンアミド、アゾビスイソブ
チロニトリル、ジニトロソペンタメチレンテトラ
ミン、パラトルエンスルホニルヒドラジド、4,
4′−オキシビスベンゼンスルホニルヒドラジド等
の有機発泡剤、重炭酸ナトリウム、炭酸アンモニ
ウム、重炭酸アンモニウム、アジド化合物、ホウ
水素化ナトリウム等の無機発泡剤などが挙げられ
る。発泡剤の望ましい添加量は、塩化ビニル樹脂
100重量部に対して1重量部から30重量部の範囲
である。 本発明において、樹脂組成物発泡体を被覆する
基体としては、紙、布、不織布、木板などを使用
することができる。 また、樹脂組成物発泡体と基体との間に設ける
水不透過層は、非発泡の塩化ビニル樹脂、熱可塑
性ポリウレタン樹脂、アクリル樹脂、EVA(エチ
レン−酢酸ビニル共重合)樹脂、酢酸ビニル樹
脂、ポリアミド樹脂など、実質上水を透過せず、
塩化ビニル樹脂との接着性が良好なものであれば
よいがなかでも、塩化ビニル樹脂発泡体に対する
接着性が特によく、成形加工も容易である非発泡
の塩化ビニル樹脂による層を設けるのが、とりわ
け好ましい。 本発明のビニル壁材を構成する塩化ビニル樹脂
発泡体は、ペースト加工法、カレンダー加工法、
押出加工法のいずれの方法で得られたものでもよ
い。また、この発泡体と基体との間に水不透過層
を設けるにあたつても、基体上に水不透過層を被
覆し、その上に塩化ビニル樹脂発泡体層を形成せ
しめる方法、水不透過層を被覆した基体の水不透
過面に塩化ビニル樹脂発泡体を一体化させる方
法、水不透過層を有する塩化ビニル樹脂発泡体の
水不透過面を基体と一体化させる方法、塩化ビニ
ル樹脂発泡体と基体との一体化と同時に接着面に
水不透過層を形成せしめる方法など、任意の方法
を採用することができる。 本発明のビニル壁材を製造する実施態様の一例
として、ペースト加工法により、非発泡の塩化ビ
ニル樹脂層および塩化ビニル樹脂発泡層を設ける
場合について説明する。まず、発泡剤を含まない
非発泡性塩化ビニルプラスチゾルを、紙、織布、
編布、不織布などの基体上に、ドクターナイフ
法、ロールコーター法などにより、できるだけ薄
く、一定の厚みで塗布したのち、120℃〜170℃で
10秒ないし5分間加熱して、プラスチゾルをゲル
化させる。その後、この非発泡塩化ビニル樹脂層
で被覆した基体の塩化ビニル樹脂層側にさらに、
高吸水性高分子、可塑剤、発泡剤および必要によ
りその他補助剤を含有する塩化ビニルプラスチゾ
ルを上記と同様な方法で塗布し、180℃〜250℃で
30秒ないし5分間加熱し、発泡させる。これによ
り、基体と発泡層の間に非発泡の塩化ビニル樹脂
層を有するビニル壁材が得られる。 本発明のビニル壁材はシート状であり、室内壁
面、押入れの壁、天井などに貼つて結露を防止す
るものであることから、この壁材は適切な厚さに
すべきである。容易に理解されるとおり、壁材の
結露防止効果、すなわちその保水量は、厚さによ
つても異なるからである。壁材として必要な厚さ
は0.1〜3mmであり、とりわけ0.3〜1.5mmが適当で
ある。 本発明のビニル壁材は、構成においても製造法
においても多くの変更態様が可能である。例え
ば、表面に壁材製品として適切な表面処理や柄付
けをしたり、エンボス加工を施したりすることは
もちろん、裏面に粘着剤を塗布して剥離紙を当て
るなど、通常の壁材製品について行われることは
すべて取り入れることができる。特にエンボス加
工は、表面積を大きくして水分を吸収しやすい形
状とする効果があるので、施すのが好ましい。表
面処理や柄付けをする場合は、処理剤を全面に塗
布すると被膜ができて吸水性を悪くすることがあ
るので、メツシユロールなどを使用して処理する
のが好ましい。 本発明の結露防止用ビニル壁材を使用すること
により、雨季などの湿度の多い時でも、結露した
水分は壁材を構成する塩化ビニル樹脂発泡体層に
吸収され、表面に水滴が現われることがないの
で、表面への結露が防止される。またこのビニル
壁材は、塩化ビニル樹脂発泡体層に吸収された水
分が裏打ちの基体に移行しないので、水分による
基体の伸び、さらにはかびの発生や腐敗による糊
材の劣化が防止され、その結果、きれいに貼つた
状態が長期間にわたつて維持される。さらにこの
ビニル壁材は、高湿度下では急速に水分を吸収す
る一方、低湿度下では水分を放出するという、い
わゆる呼吸性を有するので、小さな部屋などでは
湿度調節の目的で使用することもできる。 以上詳述した本発明の結露防止用ビニル壁材
は、居間、台所、トイレ、風呂場、洗面所、押入
れなど、住居の壁や天井の内装材として使用でき
るばかりでなく、コンテナーなどにおける内壁の
結露防止用壁材としても利用することができる。 以下に実施例を挙げて、本発明の結露防止用ビ
ニル壁材をさらに具体的に説明するが、本発明は
これらに限定されるものではない。 実施例 1〜2 酢酸ビニル60gとアクリル酸メチル40gに、重
合開始剤としてラウロイルパーオキシド0.1gを
加え、部分ケン化ポリビニルアルコール3gと
NaCl 10gを含む水300ml中に撹拌分散せしめ、
65℃で6時間懸濁重合した。この共重合体86g
を、メタノール200g、水10gおよび5NのNaOH
水溶液40mlからなるケン化液中に懸濁し、25℃で
1時間、次いで65℃で5時間ケン化反応を行つ
た。メタノールで充分洗浄したあと減圧乾燥し
て、平均粒径200μのケン化物(吸水倍率700g/
gの吸水能力を有する)を得た。これをジエツト
ミル粉砕して、粒径60μ以下の微粉状高吸水性高
分子を得た。 この高吸水性高分子と塩化ビニル樹脂を用い、
第1表に示す配合物をデスパーにより混合撹拌し
て、均一なペースト状の発泡層用塩化ビニルプラ
スチゾル組成物を調製した。
The present invention relates to a vinyl wall material for preventing dew condensation. More specifically, in wallpaper, ceiling covering materials, etc.
This invention relates to a sheet-shaped vinyl wall material that prevents the formation of water droplets due to dew condensation and has improved mildew resistance. Paper,
Often used are cloth, nonwoven fabric, or other substrates treated with resin, or plastic sheets themselves. For example, wall materials made of paper, cloth, or non-woven fabric processed with vinyl chloride resin have advantages such as strong tensile and tear strength, excellent water resistance, and the ability to easily wipe away dirt. Since then, it is now used in living rooms, closets, kitchens, toilets, etc. However, this wall material has poor hygroscopicity, so moisture condenses on the surface of the wall material due to large temperature differences between indoors and outdoors, or sudden changes in room temperature or humidity.
It has the disadvantage that it appears as water droplets.
When moisture condenses on the surface, problems such as stains and mold growth occur. Also, especially if there is condensation on the walls of the closet in your residence,
Futons and other items become damp, uncomfortable, and unsanitary. As a means to improve the drawbacks of wall materials made by processing paper, cloth, or nonwoven fabric with vinyl chloride resin, superabsorbent polymers, vinyl chloride resin,
Foamed paper, which is made by applying a paste sol consisting of a plasticizer and foaming agent to a substrate such as paper and then heating it to foam, has high water absorption and water retention properties, so this foamed paper is used to prevent condensation. It has been proposed to be used as wall material (Japanese Patent Publication No.
56-33032). Although the wall material described in this bulletin is highly effective in preventing dew condensation, some of the moisture absorbed by the foam layer transfers to the backing base and the adhesive used to attach the wall material. As a result, the base material in that area may stretch, causing sagging or wrinkles on the surface of the wall material that was neatly pasted, or the adhesive may become moldy or rot, causing the area to deteriorate.
There were points that needed further improvement. In view of these circumstances, the inventors of the present invention conducted further intensive studies on vinyl chloride wall materials that can prevent the generation of water droplets due to dew condensation, and as a result, a foam layer mainly composed of vinyl chloride resin containing super absorbent polymers was developed. By providing a water-impermeable layer between the base layer and the base layer, there will be no wrinkles due to the stretch of the base and no mold will develop in the glue material, and there will be no sagging or peeling from the wall material even after long-term use. They discovered that it could be used as a wall and completed the present invention. That is, the present invention provides a sheet consisting of a resin composition foam layer consisting of a synthetic resin mainly composed of vinyl chloride resin, a superabsorbent polymer, a plasticizer, and any other auxiliary agents, and a base layer covering the foam layer. The present invention provides a vinyl wall material for preventing dew condensation, further comprising a water-impermeable layer between the foam layer and the base layer. Since the vinyl wall material of the present invention is a resin foam containing a super absorbent polymer in the part that comes into contact with the outside air, when the temperature of the wall becomes below the dew point of the air in contact with it and water vapor in the air becomes condensed water. The condensed water is quickly absorbed into the resin and retained within the super absorbent polymer. Therefore, condensation is prevented.
Furthermore, since the resin layer is a foam, condensed water is absorbed into the resin very quickly, and it has excellent dew condensation prevention effects. Furthermore, since this wall material has a water-impermeable layer between the foam layer and the base layer, absorbed moisture does not penetrate to the base, and there is virtually no stretching of the base or deterioration of the adhesive due to moisture. I won't wake you up. Therefore, the vinyl wall material of the present invention has the advantage that when used by pasting it on a wall surface, it remains neatly pasted for a long period of time. The superabsorbent polymer used in the resin composition foam layer of vinyl wall materials absorbs water and expands from several times to several thousand times its weight, and although it retains water, it does not dissolve in water. If there is, it can be anything. just,
If the amount of water absorbed is less than 30 times its own weight, a large amount of super absorbent polymer will be needed to absorb the condensed water, which will reduce the mechanical strength of the vinyl wall material such as tensile strength and tearing. The amount of water absorbed by the superabsorbent polymer used is preferably 30 times or more its own weight. There are no particular restrictions on the shape or particle size of the superabsorbent polymer, but from the viewpoint of processability and physical properties of vinyl wall materials, it is desirable that the particle size be as small as possible, with an average particle size of 100μ or less,
Furthermore, it is better to use a material of 50μ or less. As super absorbent polymers, various known ones,
For example, saponified graft copolymers of starch and acrylonitrile, graft copolymers of starch and acrylic acid or its salts, salts of copolymers of styrene and maleic anhydride, and copolymers of isobutylene and maleic anhydride. Crosslinked polymer salts, crosslinked polymers of acrylic acid and/or acrylates (self-crosslinked polymers, crosslinked polymers obtained by polymerization in the coexistence of a crosslinking agent, post-crosslinked polymers, etc.), polyvinyl Salt of reaction product of alcohol and maleic anhydride,
Graft copolymers of polyvinyl alcohol and acrylic acid or its salts, saponified copolymers of vinyl esters and ethylenically unsaturated carboxylic acids or derivatives thereof, copolymers of vinyl esters and unsaturated polyhydric carboxylic acids or derivatives thereof Saponified copolymers, polyvinyl alcohol crosslinked products, polyethylene glycol crosslinked products, carboxymethylcellulose crosslinked products, polyvinylpyrrolidone crosslinked products, polyacrylamide crosslinked products, saponified polyacrylonitrile products, and mixtures thereof can be used. Among these, it is preferable to use a superabsorbent polymer made of a polymer electrolyte containing a carboxylic acid and/or its salt having a crosslinked structure because it has a high water absorption capacity and excellent strength after water absorption. . In particular, a copolymer consisting mainly of vinyl ester (X) and ethylenically unsaturated carboxylic acid or its derivative (Y), with a molar ratio of X:Y = 10:90 to 90:10. Compounds are particularly preferred because they have high strength after water absorption, excellent weather resistance and heat resistance in a water-absorbed state, and the dew condensation prevention effect of a wall material for preventing condensation using this compound lasts for a long period of time. The desirable amount of the super absorbent polymer added is in the range of 1 part by weight to 200 parts by weight per 100 parts by weight of the vinyl chloride resin. If the amount of super absorbent polymer is less than 1 part by weight, the hygroscopicity will be so small that dew condensation cannot be sufficiently prevented;
If it exceeds the weight part, the strength as a wall material will be insufficient. Therefore, it is preferable to use the superabsorbent polymer within the above range, and more preferably from 5 parts by weight to 150 parts by weight per 100 parts by weight of vinyl chloride resin.
Used in parts by weight. In the vinyl wall material of the present invention, the vinyl chloride resin used in the resin composition foam layer is a vinyl chloride polymer, a vinyl chloride copolymer, or a mixture thereof, and is polymerized by suspension polymerization, emulsion polymerization, etc. It may be legally obtained and commonly used, and there are no special restrictions on its type. Furthermore, various modifiers such as other resins such as PMMA, MBS, ABS, EVA, etc. may be added. Plasticizers added to vinyl chloride resin include:
The usual one is used. Furthermore, for flame retardancy, it is desirable to use an organic phosphoric acid plasticizer together. Examples of common plasticizers include phthalate esters such as dioctyl phthalate, dibasic acid esters such as 2-ethylhexyl adipate and dioctyl sebacate, epoxidized soybean oil, epoxidized linseed oil, and epoxy hexahydrocarbonate. Examples include epoxides such as dioctyl phthalate, poly(propylene adipate), poly(1,3-butylene sebacate), dihydric alcohol esters such as ethylene phthalyl glycol, and chlorinated paraffins. Examples of organic phosphoric acid plasticizers include tricresyl phosphate, cresyl phenyl phosphate, monooctyl diphenyl phosphate, trioctyl phosphate, triphenyl phosphate, tributoxyethyl phosphate, and tributyl phosphate. The desired amount of plasticizer used is vinyl chloride resin.
The amount ranges from 30 parts by weight to 150 parts by weight per 100 parts by weight, and within this range, any ratio can be taken depending on the purpose. Furthermore, commonly used adjuvants may be added to the vinyl chloride resin constituting the vinyl wall material of the present invention, if necessary. The addition ratio of adjuvant is
It can be changed as appropriate depending on the desired product. Examples of such adjuvants include stabilizers, inorganic fillers such as calcium carbonate and clay, pigments,
Examples include diluents, flame retardants, and fungicides. The resin composition foam constituting the vinyl wall material of the present invention can generally be obtained by any known method for producing vinyl chloride resin foam, and there are no particular restrictions on the production method. For example, a method of heating a paste containing the above-mentioned raw materials to gel it while mechanically creating air bubbles by blowing gas or steam into it or stirring it; A blowing agent that decomposes to generate gas is added and mixed in advance.
A method of heating and gelling and foaming at the same time, or
It can be obtained by heating to gel and then foaming by further heating at a high temperature. Among these methods, the method of using a foaming agent has fine foam cells, uniform distribution, high strength, and a foam with a good finished appearance.
This method is preferable as a method for obtaining a resin composition foam constituting the vinyl wall material of the present invention. Foaming agents that can be used include azodicarbonamide, azobisisobutyronitrile, dinitrosopentamethylenetetramine, paratoluenesulfonylhydrazide, 4,
Examples include organic blowing agents such as 4'-oxybisbenzenesulfonyl hydrazide, and inorganic blowing agents such as sodium bicarbonate, ammonium carbonate, ammonium bicarbonate, azide compounds, and sodium borohydride. The desired amount of blowing agent added is vinyl chloride resin.
The amount ranges from 1 part by weight to 30 parts by weight per 100 parts by weight. In the present invention, paper, cloth, nonwoven fabric, wooden board, etc. can be used as the substrate for covering the resin composition foam. In addition, the water-impermeable layer provided between the resin composition foam and the substrate may include non-foamed vinyl chloride resin, thermoplastic polyurethane resin, acrylic resin, EVA (ethylene-vinyl acetate copolymer) resin, vinyl acetate resin, Materials such as polyamide resin, which are virtually impermeable to water,
Any material that has good adhesion to vinyl chloride resin may be used, but it is preferable to provide a layer made of non-foamed vinyl chloride resin, which has particularly good adhesion to vinyl chloride resin foam and is easy to mold. Particularly preferred. The vinyl chloride resin foam constituting the vinyl wall material of the present invention can be processed by paste processing, calendar processing,
It may be obtained by any extrusion method. In addition, when providing a water-impermeable layer between this foam and a substrate, there are methods of coating a water-impermeable layer on the substrate and forming a vinyl chloride resin foam layer thereon. A method for integrating a vinyl chloride resin foam into a water-impermeable surface of a substrate coated with a permeable layer, a method for integrating a water-impermeable surface of a vinyl chloride resin foam having a water-impermeable layer with a substrate, a vinyl chloride resin Any method can be used, such as a method of forming a water-impermeable layer on the adhesive surface simultaneously with the integration of the foam and the base. As an example of an embodiment for manufacturing the vinyl wall material of the present invention, a case will be described in which a non-foamed vinyl chloride resin layer and a vinyl chloride resin foam layer are provided by a paste processing method. First, non-foaming vinyl chloride plastisol, which does not contain a blowing agent, is applied to paper, woven fabric,
After applying it to a substrate such as knitted fabric or non-woven fabric using the doctor knife method or roll coater method to a constant thickness as thin as possible, it is heated at 120℃ to 170℃.
Heat for 10 seconds to 5 minutes to gel the plastisol. Then, on the vinyl chloride resin layer side of the base coated with this non-foamed vinyl chloride resin layer,
Apply vinyl chloride plastisol containing a super absorbent polymer, a plasticizer, a blowing agent, and other auxiliary agents as necessary in the same manner as above, and heat it at 180°C to 250°C.
Heat for 30 seconds to 5 minutes to foam. As a result, a vinyl wall material having a non-foamed vinyl chloride resin layer between the base and the foam layer is obtained. Since the vinyl wall material of the present invention is in the form of a sheet and is applied to indoor walls, closet walls, ceilings, etc. to prevent condensation, this wall material should have an appropriate thickness. This is because, as is easily understood, the dew condensation prevention effect of a wall material, that is, its water retention capacity, differs depending on its thickness. The required thickness for the wall material is 0.1 to 3 mm, with 0.3 to 1.5 mm being particularly suitable. The vinyl wall material of the present invention is capable of many modifications, both in construction and manufacturing method. For example, in addition to applying appropriate surface treatments, patterns, and embossing to the surface of wall materials, we also apply adhesive to the back and apply release paper, which are similar to regular wall materials. You can take in everything that comes your way. In particular, embossing is preferable because it has the effect of increasing the surface area and creating a shape that easily absorbs moisture. If surface treatment or patterning is to be applied, it is preferable to use a mesh roll or the like, as applying a treatment agent to the entire surface may form a film that may impair water absorption. By using the dew condensation prevention vinyl wall material of the present invention, even in times of high humidity such as during the rainy season, condensed water is absorbed by the vinyl chloride resin foam layer that makes up the wall material, preventing water droplets from appearing on the surface. This prevents condensation on the surface. In addition, with this vinyl wall material, moisture absorbed by the PVC resin foam layer does not transfer to the backing base, which prevents the base from stretching due to moisture and deterioration of the glue material due to mold and rot. As a result, the adhesive remains neatly applied for a long period of time. Furthermore, this vinyl wall material has a so-called breathable property, meaning that it rapidly absorbs moisture under high humidity conditions, but releases moisture under low humidity conditions, so it can be used to control humidity in small rooms. . The condensation-preventing vinyl wall material of the present invention described in detail above can be used not only as an interior material for walls and ceilings in living rooms, kitchens, toilets, bathrooms, washrooms, closets, etc., but also for interior walls in containers, etc. It can also be used as a wall material to prevent condensation. The vinyl wall material for preventing dew condensation of the present invention will be explained in more detail with reference to Examples below, but the present invention is not limited thereto. Examples 1-2 0.1 g of lauroyl peroxide was added as a polymerization initiator to 60 g of vinyl acetate and 40 g of methyl acrylate, and 3 g of partially saponified polyvinyl alcohol was added.
Stir and disperse in 300 ml of water containing 10 g of NaCl,
Suspension polymerization was carried out at 65°C for 6 hours. 86g of this copolymer
, 200g methanol, 10g water and 5N NaOH
The suspension was suspended in a saponification solution consisting of 40 ml of an aqueous solution, and the saponification reaction was carried out at 25°C for 1 hour and then at 65°C for 5 hours. After thoroughly washing with methanol and drying under reduced pressure, a saponified product with an average particle size of 200μ (water absorption capacity of 700g/
) was obtained. This was pulverized with a jet mill to obtain a finely powdered superabsorbent polymer having a particle size of 60 μm or less. Using this super absorbent polymer and vinyl chloride resin,
The formulations shown in Table 1 were mixed and stirred using a despar to prepare a uniform pasty vinyl chloride plastisol composition for a foam layer.

【表】 (注) 表中の数値は重量部である。
一方、上記配合物よりあらかじめアゾジカーボ
ンアミドと高吸水性高分子を除いた配合物を同様
にペースト化し、非発泡性塩化ビニルプラスチゾ
ルを調製した。 次に紙材上に、上記非発泡性塩化ビニルプラス
チゾルを0.1mm厚でナイフコーテイングし、続い
て150℃で30秒加熱してゲル化せしめた。さらに
その上に、上記発泡層用塩化ビニルプラスチゾル
を0.2mm厚で同様にコーテイングし、220℃で1分
間加熱して発泡させ、エンボスロールによりエン
ボス加工を施して、シート状のビニル壁材を得
た。 比較例1:水不透過層なしの場合 紙上に、あらかじめ非発泡性塩化ビニル層をコ
ーテイングせず、実施例2の配合による発泡層を
実施例と同様の方法で被覆せしめた従来技術によ
るビニル壁材を得た。 比較例2:高吸水性高分子なしの場合 実施例2の配合よりあらかじめ高吸水性高分子
を除いた配合物を用意し、実施例と同様にペース
ト化して紙上にコーテイングし、加熱発泡せしめ
てビニル壁材を得た。 比較例3:発泡なしの場合 実施例2の配合よりあらかじめアゾジカーボン
アミドを除いた配合物を用意し、実施例と同様に
ペースト化して紙の上にコーテイングし、加熱ゲ
ル化せしめてビニル壁材を得た。 実用試験 1 上記実施例1および2ならびに比較例1,2お
よび3のビニル壁材それぞれについて、室内温度
35℃、相対湿度90%、壁材裏面温度10℃の条件で
結露性試験を行つた。その結果を第2表に示す。 実施例1および2の壁材は結露がなく、24時間
後もまつたく変化がみられなかつた。これに対
し、比較例1の壁材は、表面の感触は実施例1お
よび2と同様であつたが、一部に壁材のたるみを
生じていた。比較例2および3の壁材は結露を生
じ、壁面を水が滴下していた。
[Table] (Note) Values in the table are parts by weight.
On the other hand, a non-foamable vinyl chloride plastisol was prepared by preparing a paste by removing azodicarbonamide and a superabsorbent polymer from the above-mentioned mixture. Next, the above non-expandable vinyl chloride plastisol was coated with a knife to a thickness of 0.1 mm on the paper material, and then heated at 150° C. for 30 seconds to gel it. Furthermore, the above-mentioned vinyl chloride plastisol for the foam layer was similarly coated with a thickness of 0.2 mm, heated at 220°C for 1 minute to foam, and embossed with an embossing roll to obtain a sheet-like vinyl wall material. Ta. Comparative Example 1: Case without water-impermeable layer Vinyl wall according to the prior art in which paper was not coated with a non-foamable vinyl chloride layer in advance, but a foam layer with the formulation of Example 2 was coated in the same manner as in Example. I got the material. Comparative Example 2: Without superabsorbent polymer A blend was prepared by removing the superabsorbent polymer from the blend of Example 2, and the paste was made into a paste and coated on paper in the same manner as in the example, followed by heating and foaming. Obtained vinyl wall material. Comparative Example 3: No foaming A mixture of Example 2 with the azodicarbonamide removed in advance was prepared, made into a paste in the same manner as in Example, coated on paper, heated to gel, and made into a vinyl wall. I got the material. Practical Test 1 For each of the vinyl wall materials of Examples 1 and 2 and Comparative Examples 1, 2, and 3, the indoor temperature was
A dew condensation test was conducted under the conditions of 35°C, relative humidity of 90%, and temperature on the back of the wall material of 10°C. The results are shown in Table 2. The wall materials of Examples 1 and 2 had no dew condensation, and no noticeable change was observed even after 24 hours. On the other hand, the wall material of Comparative Example 1 had the same surface feel as Examples 1 and 2, but had some sagging in the wall material. The wall materials of Comparative Examples 2 and 3 had condensation, and water was dripping down the wall surface.

【表】【table】

【表】 実用試験 2 上記実施例1および2ならびに比較例1および
2のビニル壁材をそれぞれ、夜間結露する壁面に
通常の澱粉糊を使用して貼り付け、その結露防止
効果、長期間使用後の変形などを調べた。その結
果を第3表に示した。 昼間の温度が高いときは、4種のサンプルのい
ずれも乾燥状態にあつた。しかし夜になると差が
認められ、実施例1および2ならびに比較例1の
壁材はサラツとした感触を保つていたが、比較例
2の壁材は結露を生じて表面が湿つていた。再び
温度が高く湿度の低い条件になると、各サンプル
とも乾燥状態となつた。60日間の継続観察の終わ
りには、実施例1および2の壁材は貼り付けたま
まの状態で変化がなかつたが、比較例1の壁材は
壁面との剥離が生じ、剥離部分にはかびが発生し
ていた。比較例2の壁材にはたるみが生じ、表面
はかびやシミなどにより汚れていた。 一方、比較例1の壁材を、疎水性と耐水性を有
する接着剤を使用して壁面に貼り付けた場合につ
いても、同様の試験を行つた。結果は第3表に示
したとおりであり、壁材と壁面との剥離は生じな
かつたが、壁材のたるみによるしわが生じてい
た。
[Table] Practical Test 2 The vinyl wall materials of Examples 1 and 2 and Comparative Examples 1 and 2 above were respectively pasted on walls where dew condenses at night using normal starch glue, and their dew condensation prevention effects were evaluated after long-term use. We investigated the deformation of The results are shown in Table 3. When the daytime temperature was high, all four samples were in a dry state. However, at night, a difference was observed: the wall materials of Examples 1 and 2 and Comparative Example 1 maintained a smooth feel, while the wall materials of Comparative Example 2 had condensation and had a damp surface. When the temperature was high and the humidity was low again, each sample became dry. At the end of 60 days of continuous observation, the wall materials of Examples 1 and 2 remained attached with no change, but the wall materials of Comparative Example 1 had peeled from the wall surface, and the peeled portions had no change. There was mold. The wall material of Comparative Example 2 was sagging, and the surface was dirty with mold and stains. On the other hand, a similar test was also conducted on a case where the wall material of Comparative Example 1 was attached to a wall surface using an adhesive having hydrophobicity and water resistance. The results are shown in Table 3, and although no peeling occurred between the wall material and the wall surface, wrinkles did occur due to sagging of the wall material.

【表】 △ 部分的にあり
× 全体にあり
[Table] △ Partially present
× Available throughout

Claims (1)

【特許請求の範囲】 1 塩化ビニル樹脂、高吸水性高分子および可塑
剤からなる樹脂組成物発泡体層と、それを被覆す
る基体層とよりなるシートであつて、さらに前記
発泡体層と前記基体層との間に、非発泡の塩化ビ
ニル樹脂で構成される水不透過層を設けたことを
特徴とする結露防止用ビニル壁材。 2 高吸水性高分子が、カルボン酸および/また
はその塩を含む架橋構造を有する高分子電解質で
ある特許請求の範囲第1項記載の結露防止用ビニ
ル壁材。 3 高吸水性高分子が、ビニルエステル(X)とエチ
レン系不飽和カルボン酸またはその誘導体(Y)を主
成分として、X:Y=10:90〜90:10なる範囲の
モル比で構成される共重合体のケン化物である特
許請求の範囲第1項記載の結露防止用ビニル壁
材。
[Scope of Claims] 1. A sheet comprising a resin composition foam layer comprising a vinyl chloride resin, a superabsorbent polymer, and a plasticizer, and a base layer covering the same, further comprising the foam layer and the A vinyl wall material for preventing dew condensation, characterized in that a water-impermeable layer made of non-foamed vinyl chloride resin is provided between the base layer and the base layer. 2. The vinyl wall material for preventing dew condensation according to claim 1, wherein the super absorbent polymer is a polymer electrolyte having a crosslinked structure containing a carboxylic acid and/or a salt thereof. 3. The super absorbent polymer is composed of vinyl ester (X) and ethylenically unsaturated carboxylic acid or its derivative (Y) in a molar ratio of X:Y = 10:90 to 90:10. The vinyl wall material for preventing dew condensation according to claim 1, which is a saponified product of a copolymer.
JP58189023A 1983-10-07 1983-10-07 Condensation-proofing vinyl wall covering Granted JPS6081378A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58189023A JPS6081378A (en) 1983-10-07 1983-10-07 Condensation-proofing vinyl wall covering

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58189023A JPS6081378A (en) 1983-10-07 1983-10-07 Condensation-proofing vinyl wall covering

Publications (2)

Publication Number Publication Date
JPS6081378A JPS6081378A (en) 1985-05-09
JPH0524273B2 true JPH0524273B2 (en) 1993-04-07

Family

ID=16234005

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58189023A Granted JPS6081378A (en) 1983-10-07 1983-10-07 Condensation-proofing vinyl wall covering

Country Status (1)

Country Link
JP (1) JPS6081378A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62231740A (en) * 1986-04-01 1987-10-12 日本ビニル工業株式会社 Hygroscopic and damp-discharging vinyl wall material and manufacture thereof
JPS62187730U (en) * 1986-05-20 1987-11-30
JPH02279324A (en) * 1989-04-20 1990-11-15 Toyo Tire & Rubber Co Ltd Humidity conditioning foamed sheet and preparation thereof
JPH0494438U (en) * 1990-12-26 1992-08-17

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5438614A (en) * 1977-09-01 1979-03-23 Taiho Kogyo Co Ltd Method of adjusting interior humidity of building and preventing dewing on wall
JPS5633032A (en) * 1979-08-27 1981-04-03 Sumitomo Chem Co Ltd Material having water absorbing and water-holding capacity
JPS5791262A (en) * 1980-11-29 1982-06-07 Seibu Polymer Kasei Kk Wall sheath material
JPS57208236A (en) * 1981-06-19 1982-12-21 Nippon Synthetic Chem Ind High-water absorbing laminate

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5438614A (en) * 1977-09-01 1979-03-23 Taiho Kogyo Co Ltd Method of adjusting interior humidity of building and preventing dewing on wall
JPS5633032A (en) * 1979-08-27 1981-04-03 Sumitomo Chem Co Ltd Material having water absorbing and water-holding capacity
JPS5791262A (en) * 1980-11-29 1982-06-07 Seibu Polymer Kasei Kk Wall sheath material
JPS57208236A (en) * 1981-06-19 1982-12-21 Nippon Synthetic Chem Ind High-water absorbing laminate

Also Published As

Publication number Publication date
JPS6081378A (en) 1985-05-09

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