JPS6036391B2 - Method of manufacturing foam decorative material - Google Patents

Method of manufacturing foam decorative material

Info

Publication number
JPS6036391B2
JPS6036391B2 JP56035426A JP3542681A JPS6036391B2 JP S6036391 B2 JPS6036391 B2 JP S6036391B2 JP 56035426 A JP56035426 A JP 56035426A JP 3542681 A JP3542681 A JP 3542681A JP S6036391 B2 JPS6036391 B2 JP S6036391B2
Authority
JP
Japan
Prior art keywords
foaming
layer
synthetic resin
blowing agent
agent
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
Application number
JP56035426A
Other languages
Japanese (ja)
Other versions
JPS57150545A (en
Inventor
昭徳 関
一雄 笠原
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.)
Kanto Leather Cloth Co Ltd
Original Assignee
Kanto Leather Cloth 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 Kanto Leather Cloth Co Ltd filed Critical Kanto Leather Cloth Co Ltd
Priority to JP56035426A priority Critical patent/JPS6036391B2/en
Publication of JPS57150545A publication Critical patent/JPS57150545A/en
Publication of JPS6036391B2 publication Critical patent/JPS6036391B2/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/02Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles
    • B29C44/04Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles consisting of at least two parts of chemically or physically different materials, e.g. having different densities
    • B29C44/0461Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles for articles of definite length, i.e. discrete articles consisting of at least two parts of chemically or physically different materials, e.g. having different densities by having different chemical compositions in different places, e.g. having different concentrations of foaming agent, feeding one composition after the other

Description

【発明の詳細な説明】 本発明は省材料という時代の要請にも答えられ、しかも
従来の発泡倍率の観念によってしては信じられない程の
極端に大きな凹凸差を具備せしめた発泡装飾材の製造方
法に関するものである。
[Detailed Description of the Invention] The present invention is a foamed decorative material that can meet the demands of the era of material saving and has an extremely large unevenness difference that would be unbelievable based on the conventional concept of foaming ratio. This relates to a manufacturing method.

従来、発泡製品である装飾材を得るには発泡表面が荒れ
る一歩手前の発泡倍率まで発泡させ、可及的にきわだつ
た立体感、ボリューム感を出すように行なわれていた。
従って、更に顕著な立体感を増大したい場合には発泡剤
含有の樹脂量を増すことによって解決するより‘まかな
いとされていた。
Conventionally, in order to obtain decorative materials that are foamed products, foaming was carried out to a foaming ratio that was just one step before the foamed surface became rough, in order to create the most outstanding three-dimensional and voluminous feel possible.
Therefore, if it was desired to further increase the remarkable three-dimensional effect, the only solution was to increase the amount of resin containing a blowing agent.

しかし、使用樹脂量を増すということは製品重量を増す
ことであり、もし壁装材として使用する場合には、建設
省が制定している法定防火壁装材料“壁紙”として認定
条件の一つとなっている重量制限を超過してしまうほか
、コストアップにもなるし、省資源、省材料、省エネル
ギーという観点からも決して好ましい解決策とはいえな
かった。ところで、顕著な凹凸段差が得られる発泡体構
造はどうあるべきかについて考察してみると、その表層
を形成する発泡層はたとえ上記した通常の発泡倍率であ
っても、その表層の発泡層は高さ方向に大きな空洞状芯
部分の介在によって上方に向けて盛り上げられている構
造こそ望ましい態様であるといえる。
However, increasing the amount of resin used means increasing the weight of the product, and if it is to be used as a wall covering material, it will meet the requirements for certification as "wallpaper", a legal fire-retardant wall covering material established by the Ministry of Construction. This would not only exceed the current weight limit, but also increase costs, and was not a desirable solution from the standpoint of saving resources, materials, and energy. By the way, when we consider what kind of foam structure should be in order to obtain a noticeable unevenness level difference, even if the foam layer forming the surface layer has the normal foaming ratio mentioned above, the foam layer on the surface layer is It can be said that a structure in which the core is raised upward by the interposition of a large hollow core portion in the height direction is a desirable embodiment.

そこで、本発明者は如何にして前記記した高さ方向に大
きな空洞状芯部分を介在させるかについて鋭意研究を重
ねて来たが、従来公3印の分解性発泡剤の属性を巧みに
使い分けすることによって解決できることがわかり、遂
に本発明の完成を見ることができた。
Therefore, the present inventor has conducted extensive research on how to interpose a large hollow core portion in the height direction as described above, and has successfully used the attributes of the conventional three public decomposable blowing agents. It was found that the problem could be solved by doing the following, and the present invention was finally completed.

本発明を詳述すると、次の通りである。The present invention will be described in detail as follows.

発泡剤を使用する発泡法では、発泡剤として分解性発泡
剤が広く使われており、その分解性発泡剤としてはアゾ
化合物、スルホヒドラジド化合物、ニトロソ化合物、ア
ジド化合物といった有機発泡剤のほか無機発泡剤があっ
て、それぞれ分解温度やガス発生量を異にしていること
はよく知られている。
In foaming methods that use blowing agents, decomposable blowing agents are widely used as blowing agents, including organic blowing agents such as azo compounds, sulfohydrazide compounds, nitroso compounds, and azide compounds, as well as inorganic blowing agents. It is well known that there are different decomposition temperatures and amounts of gas generated.

一般に分解温度は、樹脂あるいは可塑剤、溶剤、安定剤
、酸、塩基などと混合した場合や、特に発泡剤が配合剤
に溶解した場合に大きく変わるものであるが、例えばア
ゾジカルボンアミド(ADCA)系では約20000で
あるのに対して、オキシビスベンゼンスルホニルヒドラ
ジド(0斑H)系では約130℃であるといったように
、比較的大きな分解温度差を示す二種類の分解性発泡剤
を選択することは容易である。
In general, the decomposition temperature changes greatly when mixed with resins, plasticizers, solvents, stabilizers, acids, bases, etc., and especially when blowing agents are dissolved in the compounding agent. For example, azodicarbonamide (ADCA) Select two types of decomposable blowing agents that exhibit a relatively large difference in decomposition temperature, such as approximately 20,000°C for the oxybisbenzenesulfonyl hydrazide (0% H) system, and approximately 130°C for the oxybisbenzenesulfonyl hydrazide (0% H) system. That's easy.

そこで本発明では第1−A図に示す様な、あらかじめ凹
凸模様を付与形成した基村1面の凹部に、例えばドクタ
ーナイフやコンマドクター等を用いて、第一の発泡剤含
有の合成樹脂層2を第1−B図のごとく塗布充填し、こ
れを前記発泡剤の分解温度よりも高い分解温度をもった
第二の発泡剤含有の第二の合成樹脂層3で被覆した第1
一C図の状態のものを加熱発泡処理するとした。
Therefore, in the present invention, the first foaming agent-containing synthetic resin layer is formed by using, for example, a doctor knife or a comma doctor, in the concave portions of the first surface of Motomura, which have been formed with a concavo-convex pattern in advance, as shown in Figure 1-A. 2 is coated and filled as shown in Figure 1-B, and this is covered with a second synthetic resin layer 3 containing a second blowing agent having a decomposition temperature higher than the decomposition temperature of the blowing agent.
The product in the state shown in Figure 1C was subjected to heating and foaming treatment.

然るときの第一と第二の合成樹脂層の発泡は、その初期
段階を示す第1−○図、中間の段階を示す第1−E図、
および終期段階を示す第1−F図の状態を経て完結に至
り、結局、第二の合成樹脂層の発泡層である表層を、第
二の合成樹脂層の未だ密閉性を保持した状態下で第一の
合成樹脂層が発泡した痕跡である空洞状芯部分けこより
膨出させるのであるが、各ステップを具体的に説明する
と以下のとおりである。第1−D図の発泡初期段階では
、第一の層2内の発泡剤は既に分解を開始して分解ガス
を発生し始めておるのに、これを覆う第二の層3内の発
泡剤は未だ分解する迄にはなっておらず、密閉膜の状態
がそのまま維持されておるから、第一の層2からの分解
ガスは外部に逃げることができず、第二の層3を上方に
押し上げてふくらんで行かざるを得ないoこの過程では
第一の層2内には微小なセルが散在しているが、発泡が
進むに従って微小セルは大きく生長し、更には隣のセル
同志がつながって第1−E図に見るような複数の粗大セ
ルの集合と変って行く。
The foaming of the first and second synthetic resin layers at that time is shown in Figure 1-○ showing the initial stage, Figure 1-E showing the intermediate stage,
The process is completed through the state shown in Figure 1-F, which shows the final stage, and eventually the surface layer, which is the foamed layer, of the second synthetic resin layer is removed under the condition that the second synthetic resin layer still maintains its airtightness. The hollow core portion, which is the trace of the foaming of the first synthetic resin layer, is made to bulge out. Each step is specifically explained as follows. At the initial stage of foaming shown in Figure 1-D, the foaming agent in the first layer 2 has already begun to decompose and generate decomposed gas, but the foaming agent in the second layer 3 covering it has already begun to decompose and generate decomposed gas. Since it has not yet reached the point of decomposition and the state of the sealed membrane is maintained as it is, the decomposed gas from the first layer 2 cannot escape to the outside and pushes the second layer 3 upward. In this process, the first layer 2 is scattered with tiny cells, but as the foaming progresses, the tiny cells grow larger, and furthermore, adjacent cells connect with each other. This changes into a collection of multiple coarse cells as shown in Figure 1-E.

第1一E図の状態ともなる第二の層3の発泡が徐々に始
まっているが、第一の層2からの分解ガスが自由に逃げ
られる迄にはなっていないので、前記した押し上げは益
々高さを増していく。
Although foaming of the second layer 3, which corresponds to the state shown in FIG. It keeps increasing in height.

そして複数の粗大セルがついには一つの大きな気泡とな
り、空洞状芯部分4を形成する第1−F図の発泡終期段
階では、第二の層3は適度の発泡倍率をもって発泡し、
表面は荒れることなく良好な表面状態をもった発泡体と
なるのである。基材1面の凹部の深さ、形状が一定の場
合における膨出効果を飛躍的に増大さすことになる空洞
状芯部分4の大きさは、第一の層2に含有させた発泡剤
からの分解ガス量に左右されるから、その発泡剤の量に
ついては所望する空洞状芯部分4の大きさとの関連にお
いて適宜定めればよい。
In the final stage of foaming shown in Fig. 1-F, when the plurality of coarse cells finally become one large bubble and form the hollow core portion 4, the second layer 3 is foamed with an appropriate foaming ratio.
The result is a foam with a good surface condition without any roughening. The size of the hollow core portion 4, which dramatically increases the swelling effect when the depth and shape of the recess on the base material 1 side are constant, is determined by the foaming agent contained in the first layer 2. Since the amount of blowing agent depends on the amount of decomposed gas, the amount of the blowing agent may be appropriately determined in relation to the desired size of the hollow core portion 4.

更に、基材1の凹部の深さ、形状によっても空洞状芯部
分4の大きさは左右されるが、これは最終製品としての
デザイン、意匠面を考慮して適宜選択すればよい。また
、第一と第二の発泡剤の分解温度の差が少ないと、両合
成樹脂の発泡状態のズレが余りなく、内側の第一の発泡
剤分解ガス内部に保持できずにた易く外部へ逃げてしま
って空洞状芯部分4による膨出効果に多くを期待できな
くなってしまうから、両分解温度は適宜の差を与えるべ
きで、その差は少なくとも30qo以上であることが好
ましい。
Further, the size of the hollow core portion 4 is also influenced by the depth and shape of the recessed portion of the base material 1, and this may be selected appropriately taking into consideration the design and aesthetic aspect of the final product. In addition, if the difference in decomposition temperature between the first and second blowing agents is small, there will be little deviation in the foaming state of the two synthetic resins, and the first blowing agent will not be retained in the decomposed gas inside, but will easily leak out. If the decomposition temperature escapes, we cannot expect much from the swelling effect of the hollow core portion 4, so an appropriate difference should be provided between the two decomposition temperatures, and the difference is preferably at least 30 qo or more.

尚、基材に凹凸模様を付与形成する方法は公知の方法、
例えばェンボス機、ペーパーェンボス機等によることが
できる。
In addition, the method of imparting and forming the uneven pattern on the base material is a known method,
For example, an embossing machine, a paper embossing machine, etc. can be used.

基材1の凹部に第一の合成樹脂2を塗布充填する方法は
ドクターナイフ法やコンマドクター法など公知の方法で
よく、また第二の合成樹脂はロールコーター法、ナイフ
コーター法等の塗装機で塗布できるほか、第二の発泡剤
含有合成樹脂をシート状となし、これを第一の発泡剤含
有合成樹脂を凹部に充填した基材1上に貼合わせるよう
にしてもよい。
The first synthetic resin 2 may be coated and filled into the concave portions of the base material 1 by a known method such as a doctor knife method or a comma doctor method, and the second synthetic resin may be coated with a coating machine such as a roll coater method or a knife coater method. Alternatively, the second blowing agent-containing synthetic resin may be formed into a sheet, and this may be laminated onto the base material 1 whose recesses are filled with the first blowing agent-containing synthetic resin.

以上の説明から明らかなように、本発明の方法は、表層
の発泡層を形成するための第二の発泡剤含有の合成樹脂
層3でもつて被覆された第一の発泡剤含有の合成樹脂層
2は、発泡剤分解温度の違いから第二の層3の未だ密閉
性を保持した状態下で発泡し、微細セルから粗大セル、
粗大セルから単一の空洞状芯部分4となるまで積極的に
膨脹させ、第二の層3が表層の発泡層を形成するときに
はその空洞状芯部分4の介在によって膨出させられ、樹
脂量を増さずに通常の発泡体の2〜3倍にも当る極端に
大きな凹凸段差をもった発泡装飾材が確実に得られる点
で甚だ優れている。
As is clear from the above description, the method of the present invention includes a first foaming agent-containing synthetic resin layer coated with a second foaming agent-containing synthetic resin layer 3 for forming a surface foam layer. 2, due to the difference in blowing agent decomposition temperature, foaming occurs while the second layer 3 still maintains its airtightness, and changes from fine cells to coarse cells,
The coarse cells are actively expanded until they become a single hollow core portion 4, and when the second layer 3 forms a surface foam layer, it is expanded by the intervention of the hollow core portion 4, and the amount of resin is increased. It is extremely superior in that it is possible to reliably obtain a foamed decorative material with an extremely large level difference in unevenness, which is two to three times as large as that of ordinary foam, without increasing the surface area.

凹凸のボリュームが従来程度でよいならば、本発明の方
法によるときには材料的には約半分ぐらいで済むことに
なる利点を考えると極めて経済性に富む方法といえる。
If the volume of the unevenness is the same as that of the conventional method, the method of the present invention can be said to be an extremely economical method considering the advantage that the amount of material required is about half.

また、得られた製品も軽量、ソフトで断熱性、吸音性に
優れ、復元性、緩衝作用を具備させる点で甚だ優秀であ
る。以下に実施例を示す。
In addition, the obtained product is lightweight, soft, has excellent heat insulation and sound absorption properties, and is extremely excellent in terms of resilience and cushioning properties. Examples are shown below.

本実施例のフローシートを第2図に示す。The flow sheet of this example is shown in FIG.

細かい壷状の凹凸模様をあらかじめ付与形成された厚み
0.15柳程度の壁紙鱗燃裏打紙1の凹部に、配合表A
に示す第1の発泡剤含有ポリ塩化ビニル塗料2′(発泡
剤の分解温度130qo)をナイフコーター機4にて塗
布充填した。
Mixture table A was applied to the recesses of wallpaper scale-burning backing paper 1 with a thickness of about 0.15 willow, which had been given a fine pot-like uneven pattern in advance.
A first blowing agent-containing polyvinyl chloride paint 2' (decomposition temperature of the blowing agent: 130 qo) shown in FIG.

2は基材1の凹部に充填された第一の発泡剤含有ポリ塩
化ビニル塗料の塗布層を示している。
2 shows a coating layer of the first foaming agent-containing polyvinyl chloride paint filled in the concave portion of the base material 1.

充填された塗布層2の厚みは約0.04脚であって、め
当りの該充填塗布量は極〈徴量であった。凹部分に塗布
層2を充填した髪打紙1は、つぎに120ooの乾燥炉
5内に60秒間通して乾燥ゲル化をさせてから、コータ
ー6にて配合表Bに示す第二の発泡剤含有ポリ塩化ピニ
ル塗料3′(発泡剤の分解温度20000)を全面に平
らに塗布した。
The thickness of the filled coating layer 2 was about 0.04 mm, and the estimated amount of filling was extremely small. The hair dressing paper 1 with the coating layer 2 filled in the concave portion is then passed through a 120 oo drying oven 5 for 60 seconds to dry and gel, and then a second foaming agent shown in the formulation table B is applied in the coater 6. A polychloride-containing pinyl paint 3' (decomposition temperature of blowing agent: 20,000) was applied evenly over the entire surface.

3はその第二の発泡剤含有ポリ塩化ビニル塗料の塗布層
を示している。
3 shows the coating layer of the second blowing agent-containing polyvinyl chloride paint.

該塗布層3の厚みは約0.15鰍といった通常の塗布層
厚さとした。このようにして充填塗布層2の上に塗布層
3を形成した裏打紙1は、120℃の乾燥炉7内に90
秒間通して乾燥ゲル化を行なったのち、常法に従いグラ
ビア印刷機8にてッャ消し表面処理を施してから、発泡
炉9にて220o06の砂間通して第一および第二の発
泡剤含有ポリ塩化ビニル塗料を前述のプロセスの様に発
泡ごせ冷却装置10を通して巻き取った。
The thickness of the coating layer 3 was a normal coating layer thickness of about 0.15 mm. The backing paper 1 with the coating layer 3 formed on the filling coating layer 2 in this way is placed in a drying oven 7 at 120°C for 90 minutes.
After drying and gelling for a few seconds, a gravure printing machine 8 is used to perform an anti-glare surface treatment according to a conventional method, and then the first and second foaming agent-containing polyesters are passed through a 220 o 06 sand in a foaming furnace 9. The vinyl chloride paint was spooled through the foam chiller 10 as in the process described above.

出来た製品は露玉状模様が立体的に浮き出していて、そ
の高さは約4風であった。
The resulting product had a three-dimensional dewdrop pattern that stood out, and its height was about 4 degrees.

切断端面から空洞状芯部分が形成されていて、これによ
り盛り上がっていることが明らかに確認できた。
It was clearly confirmed that a hollow core portion was formed from the cut end surface and was raised by this.

配 合 表 A (部は重量部) PVC IO悦部D〇
P 7の部安定剤
(舷−Zn系) 3部発泡剤(OB
SH系) 2$部発泡助剤
1部配 合 表 B (部は重量
部)PVC IO礎部
DOP 28部難
燃性可塑剤 2の部ェポキシ
系可塑剤 2部安定剤(軸−Zn
系) 3部発泡剤(ADCA系)
5部発泡勤剤
1.5部充填剤
5碇部顔料(Ti02)
2碇部
Blend Table A (Parts are parts by weight) PVC IO Yuebu D〇P 7 parts Stabilizer (Board - Zn system) 3 parts Foaming agent (OB
SH type) 2 parts foaming aid
1 part combination Table B (parts by weight) PVC IO base DOP 28 parts flame retardant plasticizer 2 parts epoxy plasticizer 2 parts stabilizer (axis - Zn
system) 3-part blowing agent (ADCA system)
5 parts foaming agent
1.5 parts filler
5 Ankaribe pigment (Ti02)
2nd anchor

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

第1一A図から第1一F図までは、本発明の方法の発泡
前から発泡後までの説明図である。 第2図は製造のプロセスを示すフローシートである。1
:基材、2,3:発泡剤含有合成樹脂層、4:空洞状芯
部分。 繋丁‐A図 紫’‐B図 第1‐C図 第1‐D図 発ー‐E図 第1‐F図 第2図
FIG. 11A to FIG. 11F are explanatory diagrams from before foaming to after foaming in the method of the present invention. FIG. 2 is a flow sheet showing the manufacturing process. 1
: base material, 2, 3: foaming agent-containing synthetic resin layer, 4: hollow core portion. Connection - Figure A Purple' - Figure B Figure 1 - Figure C Figure 1 - Figure D - Figure E Figure 1 - Figure 2

Claims (1)

【特許請求の範囲】[Claims] 1 凹凸模様を有する基材面の凹部に第一の発泡剤含有
の合成樹脂を充填し、これを前記発泡剤の分解温度より
も高い分解温度をもつた第二の発泡剤含有の合成樹脂で
被覆し、ついでこれを加熱発泡し、該第二の発泡剤含有
の合成樹脂層の発泡層である表層を第二の合成樹脂層の
未だ密閉性と保持した状態下で、第一の合成樹脂層が発
泡した痕跡である空洞状芯部分により膨出させることを
特徴とする発泡装飾材の製造方法。
1 A first synthetic resin containing a blowing agent is filled into the concave portions of the base material surface having an uneven pattern, and this is filled with a synthetic resin containing a second blowing agent having a decomposition temperature higher than the decomposition temperature of the blowing agent. The foamed surface layer of the second synthetic resin layer containing a foaming agent is covered with the first synthetic resin while maintaining the airtightness of the second synthetic resin layer. A method for producing a foamed decorative material, characterized in that the layer is expanded by a hollow core portion that is a trace of foaming.
JP56035426A 1981-03-13 1981-03-13 Method of manufacturing foam decorative material Expired JPS6036391B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56035426A JPS6036391B2 (en) 1981-03-13 1981-03-13 Method of manufacturing foam decorative material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56035426A JPS6036391B2 (en) 1981-03-13 1981-03-13 Method of manufacturing foam decorative material

Publications (2)

Publication Number Publication Date
JPS57150545A JPS57150545A (en) 1982-09-17
JPS6036391B2 true JPS6036391B2 (en) 1985-08-20

Family

ID=12441534

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56035426A Expired JPS6036391B2 (en) 1981-03-13 1981-03-13 Method of manufacturing foam decorative material

Country Status (1)

Country Link
JP (1) JPS6036391B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59145122A (en) * 1983-02-08 1984-08-20 Dynic Corp Preparation of expanded internal trimming material
KR100892115B1 (en) * 2007-08-03 2009-04-08 쓰리디전사지개발주식회사 Tertiary solid effervescent transcription paper with enhanced durability and its manufacturing method

Also Published As

Publication number Publication date
JPS57150545A (en) 1982-09-17

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