JPH0374907B2 - - Google Patents

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Publication number
JPH0374907B2
JPH0374907B2 JP60211870A JP21187085A JPH0374907B2 JP H0374907 B2 JPH0374907 B2 JP H0374907B2 JP 60211870 A JP60211870 A JP 60211870A JP 21187085 A JP21187085 A JP 21187085A JP H0374907 B2 JPH0374907 B2 JP H0374907B2
Authority
JP
Japan
Prior art keywords
nonwoven fabric
moisture
wall covering
covering material
humidity control
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
JP60211870A
Other languages
Japanese (ja)
Other versions
JPS6271641A (en
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 filed Critical
Priority to JP21187085A priority Critical patent/JPS6271641A/en
Publication of JPS6271641A publication Critical patent/JPS6271641A/en
Publication of JPH0374907B2 publication Critical patent/JPH0374907B2/ja
Granted legal-status Critical Current

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Description

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

(産業上の利用分野) 本発明は、室内の湿度の変動を緩和する機能を
有する調湿性壁装材料に関するものであり、その
利用は建築物の室内の他、船室、自動車内等の輸
送機械器具の産業界に幅広く利用することができ
る。 (従来の技術) 従来より、居住環境を快適にする方法として、
温度制御と湿度制御が行なわれてきた。これらの
制御の方法はエアコン等の電気エネルギー等を消
費する装置類によつて達成することが可能である
が、エネルギー消費を伴なうために経済的でない
ばかりか、居住者が不在または装置の故障等によ
り装置が運転されない場合には、制御が不能とな
りその為、結露を発生させたり、カビが繁殖し部
屋の居住環境を悪化させることがしばしばある。 また、従来より日本壁の荒土壁にみられるよう
な、材料に吸放湿の機能をもたせたパツシブ的手
法もあつた。しかし、これら吸放湿機能を持ち比
較的高い調湿力を示す材料は、非常に厚みをと
り、施工性が悪いばかりでなく、表面に内装仕上
材等で被覆されると、その調湿機能も消失するも
のであつた。 尚、ここで言う調湿力とは、温度1℃の変動に
おける単位面積当たりの吸放湿量を言い、絶対湿
度の変動量を温度の変動量で除したものに室内気
積を掛け、それを該材料の全内表面積で除したも
のである。 そして、調湿力を有するシートとして特開昭59
−9051号公報に開示されるシートがあつた。しか
し、調湿成分には重クロム酸カリウム、水酸化ナ
トリウム等を用いるものであり、潮解性、易水溶
性、毒性を有し居住環境への使用は不適であつ
た。 また、実開昭57−110214号公報に開示されるサ
イデイングの表面に粒状の吸水材料を付着させた
ものがあつたが、吸水材料の付着力、表面の凸
凹、必要個所への適用に難があつた。 (発明が解決しようとする問題点) 従来技術の問題点は、調湿機能を持つた壁の施
工性と、その壁表面を覆う壁装材料によつては調
湿力が制限される点にある。 (問題点を解決する為の手段) 本発明では、壁の表面に貼着して用いる壁装材
料に調湿力を持たせて調湿力が制限されないよう
にすると同時に薄いシート状で完成されたものと
なつていて、その施工を従来からある壁装材と同
様に容易にしている。 この為の構成として本発明では、調湿力を持つ
た材料にイソブチレンマレイン酸共重合ポリマー
を選択し、このポリマーの架橋反応を目付量80
g/m2以上の不織布上で行なわせるようにし、か
つ、貼着下地の湿気の影響を排除するためのアル
ミ箔と貼着し易くする為の防炎紙を積層するよう
にしている。 本発明の構成中、不織布は、その材質面から
は、レーヨン、ポリエステル、アクリル、テフロ
ン、ナイロン等の単独もしくは複数種類使用した
繊維等が挙げられる。また、その製造方法からは
乾式不織布(例えば、浸漬法接着剤型、フエルト
法機械結合型、短繊維法紡糸型)、湿式不織布
(例えば、フイブリカ法抄紙型、熱圧法抄紙型、
接着剤法抄紙型)などが挙げられる。 また、本発明に用いられる不織布の目付量は80
g/m2以上が望ましい。80g/m2以下では、不織布
が薄かつたり、目が荒くなり後述するポリマー溶
液の塗布の際に、不織布の表面及び裏面に均質に
浸透し、その結果本発明の調湿性壁装材料を施工
した際、室内側表面部に該ポリマーが露出し美観
上好ましくないばかりか、人が触れたりすると、
指触感が悪いばかりか、湿気以外の異物の吸着に
より調湿性能に問題が生じる。 本発明でいうイソブチレンマレイン酸共重合ポ
リマーとは、イソブチレンと無水マレイン酸の共
重合体でその組成比は、アルカリ物質と反応して
生成する組成物が水に可溶になるような範囲のも
のであればよい。 また、本発明で用いる架橋剤とは、上述のアル
カリ物質と反応して生成した水可溶性のイソブチ
レンマレイン酸共重合ポリマーを部分的に架橋し
うる化合物であればどのようなものでもよいが、
エポキシ基を分子中に2個以上有する化合物が好
ましい。それらの例としては、グリセリンジグリ
シジルエーテル、エチレングリコールジグリシジ
ルエーテル等の多価アルコール類やビスフエノー
ルAのジグリシジルエーテル、ダイマー酸グリシ
ジルエステル型エポキシ樹脂、含金属エポキシ樹
脂等が挙げられる。尚、架橋剤のイソブチレンマ
レイン酸共重合ポリマーに対する添加割合は、そ
の誘導体基に対して0.1〜5モル%の範囲が好ま
しい。この範囲以下(0.1モル%以下)では得ら
れた架橋体の吸水倍率が大き過ぎ、架橋体の膨張
の為、不織布が破れたり、貼着使用時の剥がれの
可能性が生ずる。逆に、この範囲以上(5モル%
以上)では、ゲル強度が増大しすぎ、吸水倍率が
減少してしまう。 不織布に混合溶解液を塗布するに当たつては、
まずイソブチレンマレイン酸共重合ポリマーを水
に溶解させ、増粘剤を使用し粘度を100ポイズ以
上にまで増粘させる。この増粘剤には、通常水性
塗料に使用されるものでよく、例として、ヒドロ
キシメチルセルロース、メチルセルロース、各種
アクリル酸塩、グアーガム、モンモリロナイト、
繊維状珪酸マグネシウム等が挙げられる。添加量
は添加増粘後の粘度が100ポイズ以上となるよう
に設定する。そして、架橋剤の添加、混合は塗布
直前に行なうようにする。これは、架橋反応によ
る可使時間の問題からである。粘度の設定につい
て、100ポイズ以下では前述した不織布に架橋剤
入りの混合溶解液を塗布する際に、この溶液が不
織布の塗布側に対する反対面(調湿性壁装材料と
しての使用時の室内側表面)にまで浸透してしま
う。その結果、前述の不織布の目付量の説明と同
様に美観上、指触感上および調湿性の持続という
点で問題がある。 他に上述の混合溶解液には、炭酸カルシウム、
硅石粉、マイカ、硅藻土、カオリン、タルク等の
充填剤、ハロゲン系、リン系等の難燃剤、着色顔
料、PH調整剤、分散剤等を本発明の目的を損な
わない限りにおいて使用することができる。 次に、本発明の構成要素であるアルミ箔は不透
湿層を形成して貼着下地よりの水分移動を防止す
る目的で用い、調湿性壁装材料の吸水能力を最大
まで生かすものである。 実際に使用する不透湿性と折り曲げ加工性から
アルミ箔は1μ〜50μ程度の厚みでよい。 更に、本発明に用いる防炎紙は、通常壁装材料
として壁紙の裏打紙に用いられるような防炎(難
燃)加工処理を施した紙のことをいう。 (作 用) 本発明の調湿性壁装材料はイソブチレンマレイ
ン酸共重合ポリマーの架橋体の優れた吸湿力によ
り、優れた調湿力を持つ、またその構成上、下地
材料から湿気の影響を受けることもない。更に、
施工時の表面側に位置する不織布は染色、印刷に
より任意の意匠を与えることが可能である。 (実施例) 以下、本発明の調湿性壁装材料の製造方法を図
面とともに説明する。 まず、目付量80g/m2以上の不織布1を用意す
る。一方でイソブチレンマレイン酸共重合ポリマ
ーの溶解液を増粘剤で増粘させ、粘度100ポイズ
以上にし、規定モル比の架橋剤を添加混合したも
のを作成する。次に、ナイフコーター、フローコ
ーター、バーコーター、スプレーなどの塗装装置
を使用して、前述ポリマーを含む混合溶解液2a
を不織布上に塗布する。この時、塗液は不織布の
塗装面から不織布の厚みの2/3以下で浸透が止ま
つているのがよい。架橋反応は、塗装に引き続い
て行なつた方が能率よく行なえるので、乾燥兼加
熱処理(約110℃、5分間)を塗装に続けて施す。 そして、ポリマー架橋体2bが片面兼半浸透の
状態で形成された調湿用基布10のポリマー架橋
体側に接着剤5によりアルミ箔3、更に重ねて防
炎紙4を貼り合わせることにより調湿性壁装材料
20が製造される。 以下の説明では、調湿性壁装材料の実施例と比
較例を挙げてその性能を説明する。実施例1では
目付量100g/m2のポリエステル製不織布を用意
し、イソブチレンマレイン酸共重合物ポリマー
100gに対して水300gと増粘剤としてのヒドロキ
シエチルセルロース8gの割合で混合撹拌する。
粘度が100ポイズを越えたら架橋剤としてのエチ
レングリコールジグリシジルエーテルをポリマー
比1モル%添加混合し、直ちに不織布上に約150
g/m2になるようにバーコーターにより塗布した。
次にこの塗布後の不織布を熱風乾燥器で110℃、
5分乾燥兼架橋反応させる。 乾燥後の調湿性基布のポリマー塗布側にアクリ
ル酸エステル系の接着剤によりアルミ箔12μ厚を
貼り合せ、更に、防炎紙70g/m2をアクリル酸エ
ステル系の接着剤により貼り合せた。 実施例2では、実施例1の不織布に代えて目付
量120g/m2の防炎加工したナイロン製不織布、の
エチレングリコールジグリシジルエーテルに代え
てグリセリンジグリシジルエーテルを使用し、ポ
リマー比1.5モル%添加し塗布量約150g/m2で作
成した。他は実施例1と同様にして調湿性壁装材
料を作成した。 比較例では、下記の第1俵に示すように目付量
の60g/m2、100g/m2の防炎加工したナイロン製
不織布と、イソブチレンマレイン酸共重合ポリマ
ーの溶解液の増粘後の粘度を200ポイズ、80ポイ
ズに設定し、塗布量については第1表の値(g/
m2)とし、他は実施例2と同様にして壁装材料を
作成した。 これらの実施例、比較例の外観とその調湿力
(コンクリート板10cm厚に貼り付けた時)を測定
して結果を第2表に示す。比較例には比較例5と
して、市販の壁紙を加えこの調湿力を測定した。
(Field of Industrial Application) The present invention relates to a humidity-controlling wall covering material that has the function of alleviating fluctuations in indoor humidity.The present invention can be used not only in the interiors of buildings but also in transportation machines such as ship cabins and automobiles. It can be widely used in the instrument industry. (Conventional technology) Traditionally, as a method to make the living environment comfortable,
Temperature control and humidity control have been carried out. These control methods can be achieved using devices that consume electrical energy, such as air conditioners, but they are not only uneconomical because they involve energy consumption, but also when the occupants are absent or the devices are turned off. If the device is not operated due to a malfunction or the like, control becomes impossible, which often causes condensation or mold to grow, deteriorating the living environment of the room. Additionally, there have been passive methods in which materials have moisture absorption and release functions, as seen in the rough earth walls of Japanese walls. However, these materials that have moisture absorption and desorption functions and relatively high moisture control ability are not only very thick and have poor workability, but also have poor moisture control ability when coated with interior finishing materials, etc. It was also something that would disappear. The humidity control power referred to here refers to the amount of moisture absorbed and released per unit area when the temperature fluctuates by 1°C. divided by the total internal surface area of the material. And, as a sheet with moisture control power, it was published in Japanese Patent Publication No.
-There was a sheet disclosed in Publication No. 9051. However, the humidity control ingredients used include potassium dichromate, sodium hydroxide, etc., which were deliquescent, readily water-soluble, and toxic, making them unsuitable for use in residential environments. In addition, there was a siding disclosed in Japanese Utility Model Application Publication No. 57-110214 in which granular water-absorbing material was attached to the surface of the siding. It was hot. (Problems to be Solved by the Invention) The problems of the prior art are the ease of constructing a wall with a humidity control function and the fact that the humidity control ability is limited depending on the wall covering material that covers the wall surface. be. (Means for Solving the Problems) In the present invention, the wall covering material used by pasting it on the surface of the wall has moisture control ability so that the moisture control ability is not limited, and at the same time, it can be completed in the form of a thin sheet. It has become a standard material, making its installation as easy as traditional wall coverings. As a structure for this purpose, in the present invention, an isobutylene maleic acid copolymer is selected as a material with moisture conditioning ability, and the crosslinking reaction of this polymer is
It is made to be carried out on a non-woven fabric of g/m 2 or more, and is laminated with aluminum foil to eliminate the influence of moisture on the adhesive base and flame retardant paper to make it easier to adhere. In the structure of the present invention, the nonwoven fabric may be made of fibers such as rayon, polyester, acrylic, Teflon, nylon, or the like, used alone or in combination. In addition, the manufacturing methods include dry nonwoven fabrics (e.g., dipping method adhesive type, felt method mechanical bonding type, staple fiber method spinning type), wet nonwoven fabrics (e.g., fibrica method papermaking type, thermopressure method papermaking type,
Adhesive method (paper making method), etc. In addition, the basis weight of the nonwoven fabric used in the present invention is 80
g/m 2 or more is desirable. If it is less than 80 g/m 2 , the nonwoven fabric becomes thin or rough, and when the polymer solution described below is applied, it penetrates uniformly into the front and back surfaces of the nonwoven fabric, and as a result, the moisture control wall covering material of the present invention cannot be applied. When this happens, the polymer is exposed on the indoor surface, which is not only aesthetically undesirable, but also when touched by people.
Not only does it feel bad to the touch, but adsorption of foreign substances other than moisture causes problems in humidity control performance. The isobutylene maleic acid copolymer referred to in the present invention is a copolymer of isobutylene and maleic anhydride, and the composition ratio thereof is within a range such that the composition produced by reacting with an alkaline substance is soluble in water. That's fine. Further, the crosslinking agent used in the present invention may be any compound as long as it can partially crosslink the water-soluble isobutylene maleic acid copolymer produced by reacting with the above-mentioned alkaline substance.
Compounds having two or more epoxy groups in the molecule are preferred. Examples thereof include polyhydric alcohols such as glycerin diglycidyl ether and ethylene glycol diglycidyl ether, diglycidyl ether of bisphenol A, dimer acid glycidyl ester type epoxy resins, metal-containing epoxy resins, and the like. The addition ratio of the crosslinking agent to the isobutylene maleic acid copolymer is preferably in the range of 0.1 to 5 mol % based on the derivative group thereof. Below this range (0.1 mol % or less), the water absorption capacity of the obtained crosslinked product is too high, and due to expansion of the crosslinked product, there is a possibility that the nonwoven fabric will be torn or peeled off during adhesive use. On the contrary, above this range (5 mol%
(above), the gel strength increases too much and the water absorption capacity decreases. When applying the mixed solution to the nonwoven fabric,
First, isobutylene maleic acid copolymer is dissolved in water, and a thickener is used to increase the viscosity to over 100 poise. The thickeners may be those commonly used in water-based paints, such as hydroxymethylcellulose, methylcellulose, various acrylates, guar gum, montmorillonite,
Examples include fibrous magnesium silicate. The amount added is set so that the viscosity after thickening is 100 poise or more. The addition and mixing of the crosslinking agent should be carried out immediately before coating. This is due to the pot life problem caused by the crosslinking reaction. Regarding the viscosity setting, if the viscosity is 100 poise or less, when applying the above-mentioned mixed solution containing a crosslinking agent to the nonwoven fabric, this solution will be applied to the opposite side of the nonwoven fabric to the application side (indoor surface when used as a humidity control wall covering material). ). As a result, similar to the above-mentioned explanation of the basis weight of the nonwoven fabric, there are problems in terms of aesthetic appearance, finger feel, and sustainability of humidity control. In addition, the above-mentioned mixed solution includes calcium carbonate,
Fillers such as silica powder, mica, diatomaceous earth, kaolin, and talc, flame retardants such as halogen-based and phosphorus-based flame retardants, coloring pigments, PH adjusters, dispersants, etc. may be used as long as they do not impair the purpose of the present invention. I can do it. Next, the aluminum foil, which is a component of the present invention, is used to form a moisture-impermeable layer to prevent moisture movement from the base to which it is attached, thereby maximizing the water absorption ability of the moisture-controlling wall covering material. . In view of moisture impermeability and bendability, the aluminum foil may have a thickness of about 1 μm to 50 μm in actual use. Furthermore, the flame-retardant paper used in the present invention refers to paper that has been subjected to a flame-retardant treatment, such as that which is normally used as a backing paper for wallpaper as a wall covering material. (Function) The moisture control wall covering material of the present invention has excellent moisture control ability due to the excellent moisture absorption ability of the crosslinked isobutylene maleic acid copolymer, and due to its structure, it is not affected by moisture from the base material. Not at all. Furthermore,
The nonwoven fabric located on the surface side during construction can be given any design by dyeing or printing. (Example) Hereinafter, a method for producing a moisture-controlling wall covering material of the present invention will be explained with reference to the drawings. First, a nonwoven fabric 1 having a basis weight of 80 g/m 2 or more is prepared. On the other hand, a solution of isobutylene maleic acid copolymer is thickened with a thickener to have a viscosity of 100 poise or more, and a crosslinking agent in a specified molar ratio is added and mixed to prepare a solution. Next, using a coating device such as a knife coater, flow coater, bar coater, or spray, the mixed solution 2a containing the aforementioned polymer is coated.
is applied onto the nonwoven fabric. At this time, it is preferable that the coating liquid stops permeating from the painted surface of the nonwoven fabric to 2/3 or less of the thickness of the nonwoven fabric. Since the crosslinking reaction can be carried out more efficiently after painting, a drying and heating treatment (approximately 110°C, 5 minutes) is performed immediately after painting. Then, aluminum foil 3 is laminated with adhesive 5 on the polymer crosslinked body side of the humidity control base fabric 10, in which the polymer crosslinked body 2b is formed on one side and in a semi-permeable state. Wall covering material 20 is manufactured. In the following description, examples and comparative examples of humidity control wall covering materials will be given to explain their performance. In Example 1, a polyester nonwoven fabric with a basis weight of 100 g/m 2 was prepared, and an isobutylene maleic acid copolymer polymer was prepared.
Mix and stir 100g of water at a ratio of 300g of water and 8g of hydroxyethyl cellulose as a thickener.
When the viscosity exceeds 100 poise, add and mix 1 mol% of ethylene glycol diglycidyl ether as a crosslinking agent to the polymer ratio, and immediately apply approximately 150 poise onto the nonwoven fabric.
It was coated using a bar coater so that the coating weight was 2 g/m 2 .
Next, the coated nonwoven fabric is heated at 110℃ in a hot air dryer.
Dry and crosslink for 5 minutes. After drying, a 12 μm thick aluminum foil was attached to the polymer-coated side of the moisture control base fabric using an acrylic ester adhesive, and then 70 g/m 2 of flameproof paper was attached using an acrylic ester adhesive. In Example 2, the nonwoven fabric of Example 1 was replaced with a flame-retardant nylon nonwoven fabric with a basis weight of 120 g/ m2 , and glycerin diglycidyl ether was used instead of ethylene glycol diglycidyl ether, and the polymer ratio was 1.5 mol%. The coating amount was approximately 150 g/m 2 . A humidity control wall covering material was produced in the same manner as in Example 1 except for the above. In the comparative example, as shown in the first bale below, flame-retardant nylon nonwoven fabric with a basis weight of 60 g/m 2 and 100 g/m 2 and the viscosity after thickening of the solution of isobutylene maleic acid copolymer were used. were set to 200 poise and 80 poise, and the coating amount was set to the values in Table 1 (g/
m 2 ), and a wall covering material was produced in the same manner as in Example 2 except for the following. The appearance and moisture control ability (when attached to a 10 cm thick concrete board) of these Examples and Comparative Examples were measured and the results are shown in Table 2. As Comparative Example 5, a commercially available wallpaper was added to the comparative example, and its humidity control ability was measured.

【表】【table】

【表】 続けて、調湿力の持続性をみる為に、屋外にて
3週間放置後に再度調湿力を測定した。その結果
を第3表に示した。
[Table] Subsequently, in order to see the sustainability of the humidity control power, the humidity control power was measured again after being left outdoors for 3 weeks. The results are shown in Table 3.

【表】 (発明の効果) 本発明による調湿性壁装材料は、従来の壁紙に
比べて高い調湿力を持つことが解る。また、その
調湿力も持続して発揮することが解る。 この調湿力と施工の簡便さを利用することによ
り室内温度が急激に変化することもなくなり、結
露、カビの発生をなくし、居住環境の快適化を簡
単に得られる効果がある。
[Table] (Effects of the Invention) It can be seen that the humidity control wall covering material according to the present invention has higher humidity control power than conventional wallpaper. In addition, it can be seen that its moisture regulating power is maintained continuously. By taking advantage of this humidity control ability and ease of construction, the indoor temperature will not change rapidly, eliminating dew condensation and mold growth, and making the living environment more comfortable.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の構成を示す拡大断面図であ
り、第2図は本発明の調湿性壁装材料の製法例を
示す模式図である。 1…不織布、2a…イソブチレンマレイン酸共
重合ポリマーを含む混合溶解液、2b…ポリマー
架橋体、3…アルミ箔、4…防炎紙、5…接着
剤、10…調湿用基布、20…調湿性壁装材料。
FIG. 1 is an enlarged cross-sectional view showing the structure of the present invention, and FIG. 2 is a schematic diagram showing an example of the manufacturing method of the moisture-controlling wall covering material of the present invention. 1... Nonwoven fabric, 2a... Mixed solution containing isobutylene maleic acid copolymer, 2b... Polymer crosslinked product, 3... Aluminum foil, 4... Flame retardant paper, 5... Adhesive, 10... Moisture control base fabric, 20... Humidity control wall covering material.

Claims (1)

【特許請求の範囲】[Claims] 1 目付量80g/m2以上の不織布に、粘度100ポイ
ズ以上に調整されたイソブチレンマレイン酸共重
合ポリマーと架橋剤の混合溶解液を塗布し、不織
布層途中まで浸透させ、その後加熱処理により前
記ポリマーの架橋体を不織布上で生成されたもの
に、更に前述混合溶解液塗布面にアルミ箔、防炎
紙を積層、接着したことを特徴とする調湿性壁装
材料。
1. A mixed solution of an isobutylene maleic acid copolymer and a crosslinking agent adjusted to a viscosity of 100 poise or more is applied to a nonwoven fabric having a basis weight of 80 g/m 2 or more, and the solution is allowed to penetrate halfway through the nonwoven fabric layer, and then heated to remove the polymer. A moisture-controlling wall covering material, characterized in that a crosslinked product of the above is produced on a non-woven fabric, and aluminum foil and flameproof paper are further laminated and adhered to the surface coated with the above-mentioned mixed solution.
JP21187085A 1985-09-25 1985-09-25 Humidity-conditioning wall decorative material Granted JPS6271641A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21187085A JPS6271641A (en) 1985-09-25 1985-09-25 Humidity-conditioning wall decorative material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21187085A JPS6271641A (en) 1985-09-25 1985-09-25 Humidity-conditioning wall decorative material

Publications (2)

Publication Number Publication Date
JPS6271641A JPS6271641A (en) 1987-04-02
JPH0374907B2 true JPH0374907B2 (en) 1991-11-28

Family

ID=16612978

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21187085A Granted JPS6271641A (en) 1985-09-25 1985-09-25 Humidity-conditioning wall decorative material

Country Status (1)

Country Link
JP (1) JPS6271641A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10370561B2 (en) 2016-06-28 2019-08-06 Prc-Desoto International, Inc. Urethane/urea-containing bis(alkenyl) ethers, prepolymers prepared using urethane/urea-containing bis(alkenyl) ethers, and uses thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS599051A (en) * 1982-07-07 1984-01-18 凸版印刷株式会社 Humidifying sheet

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6329762Y2 (en) * 1980-12-26 1988-08-10

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS599051A (en) * 1982-07-07 1984-01-18 凸版印刷株式会社 Humidifying sheet

Also Published As

Publication number Publication date
JPS6271641A (en) 1987-04-02

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