JPH0197632A - Manufacture of dewing preventive foaming decorative material with embossed pattern - Google Patents
Manufacture of dewing preventive foaming decorative material with embossed patternInfo
- Publication number
- JPH0197632A JPH0197632A JP62255293A JP25529387A JPH0197632A JP H0197632 A JPH0197632 A JP H0197632A JP 62255293 A JP62255293 A JP 62255293A JP 25529387 A JP25529387 A JP 25529387A JP H0197632 A JPH0197632 A JP H0197632A
- Authority
- JP
- Japan
- Prior art keywords
- foaming
- synthetic resin
- water
- moisture
- layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000005187 foaming Methods 0.000 title claims abstract description 40
- 239000000463 material Substances 0.000 title claims abstract description 39
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 230000003449 preventive effect Effects 0.000 title abstract description 3
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 85
- 239000000057 synthetic resin Substances 0.000 claims abstract description 85
- 229920005989 resin Polymers 0.000 claims abstract description 49
- 239000011347 resin Substances 0.000 claims abstract description 49
- 229920000642 polymer Polymers 0.000 claims abstract description 25
- 239000004088 foaming agent Substances 0.000 claims abstract description 24
- 238000010438 heat treatment Methods 0.000 claims abstract description 19
- 239000006260 foam Substances 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 15
- 238000010030 laminating Methods 0.000 claims description 4
- 239000000123 paper Substances 0.000 abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 8
- 150000001413 amino acids Chemical class 0.000 abstract description 4
- 229920001577 copolymer Polymers 0.000 abstract description 4
- 239000004744 fabric Substances 0.000 abstract description 4
- 239000000843 powder Substances 0.000 abstract description 3
- 239000007788 liquid Substances 0.000 abstract description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 abstract 1
- 230000002708 enhancing effect Effects 0.000 abstract 1
- 150000002735 metacrylic acids Chemical class 0.000 abstract 1
- 239000004745 nonwoven fabric Substances 0.000 abstract 1
- 230000035515 penetration Effects 0.000 abstract 1
- 239000011800 void material Substances 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
- 238000009833 condensation Methods 0.000 description 27
- 230000005494 condensation Effects 0.000 description 26
- 230000000694 effects Effects 0.000 description 17
- 239000004604 Blowing Agent Substances 0.000 description 10
- 230000035699 permeability Effects 0.000 description 9
- 230000002265 prevention Effects 0.000 description 9
- 238000000354 decomposition reaction Methods 0.000 description 8
- 238000004049 embossing Methods 0.000 description 7
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 4
- 230000001771 impaired effect Effects 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- 229940121375 antifungal agent Drugs 0.000 description 2
- 239000003429 antifungal agent Substances 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 239000003139 biocide Substances 0.000 description 2
- 239000013043 chemical agent Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005034 decoration Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 230000017525 heat dissipation Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- KINULKKPVJYRON-PVNXHVEDSA-N n-[(e)-[10-[(e)-(4,5-dihydro-1h-imidazol-2-ylhydrazinylidene)methyl]anthracen-9-yl]methylideneamino]-4,5-dihydro-1h-imidazol-2-amine;hydron;dichloride Chemical compound Cl.Cl.N1CCN=C1N\N=C\C(C1=CC=CC=C11)=C(C=CC=C2)C2=C1\C=N\NC1=NCCN1 KINULKKPVJYRON-PVNXHVEDSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- 238000010022 rotary screen printing Methods 0.000 description 2
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
- MEJAPGGFIJZHEJ-UHFFFAOYSA-N 5-acetamido-1,3,4-thiadiazole-2-sulfonyl chloride Chemical class CC(=O)NC1=NN=C(S(Cl)(=O)=O)S1 MEJAPGGFIJZHEJ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229940048053 acrylate Drugs 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002832 nitroso derivatives Chemical class 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 239000002904 solvent 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
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、壁装材や天井材等に使用される凹凸模様を有
する結露防止発泡装飾材の製造方法に関するものである
。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a method for producing a dew-preventing foam decorative material having an uneven pattern used for wall covering materials, ceiling materials, etc.
〈従来技術〉
合成樹脂を使用した装飾材に結露防止効果(透湿性)を
もたせる公知の方法としては大別して、次の三つ方法が
ある。すなわち、一つは特開昭56−3302号公報に
開示されているように、合成樹脂層に吸水性高分子を混
入することであり、もう一つは特開昭53−31772
号公報に示されているように、無数の連通ずる微細気泡
を有する発泡層とすることであり、他の一つは特公昭5
3−38102号公報に記されているように、オレフィ
ン系微多孔シートにより透湿性をもたせることである。<Prior Art> There are three known methods for imparting a dew-preventing effect (moisture permeability) to decorative materials using synthetic resins: That is, one is to mix a water-absorbing polymer into the synthetic resin layer as disclosed in JP-A-56-3302, and the other is to mix a water-absorbing polymer into the synthetic resin layer as disclosed in JP-A-53-31772.
As shown in the Japanese Patent Publication No. 1, the foam layer has countless interconnected microscopic cells.
As described in Japanese Patent No. 3-38102, the purpose is to provide moisture permeability by using an olefin-based microporous sheet.
この他に機械的に針布ロールにより微細な穴をあけるい
わゆるパンチング加工をすることにより、通気性と透湿
性を確保することもおこなわれていた。In addition, air permeability and moisture permeability were also ensured by mechanically punching fine holes using a cloth roll.
(発明が解決しようとする問題点〉
これらの装飾材は主として内装用の壁装材として用いら
れる為に、通常は機械的エンボス加工により、凹凸模様
が付与されていたが、この凹凸模様形成時に結露防止効
果(透湿性)を著しく損ない、所定の機能を発揮するこ
とが出来なかった。(Problems to be Solved by the Invention) Since these decorative materials are mainly used as interior wall covering materials, they are usually given an uneven pattern by mechanical embossing. The dew condensation prevention effect (moisture permeability) was significantly impaired and the desired function could not be achieved.
合成樹脂層に吸水性高分子を混入する方法では表面に露
出した吸水性高分子にのみ吸水作用が働くわけであるが
、装飾材としての意匠性を得る為に機械的エンボス加工
を施すと、表面に露出していた吸水性高分子の露出面積
が狭くなったり、礪端な場合は押し潰されて本来の結露
防止効果を期待できなかった。In the method of mixing water-absorbing polymers into the synthetic resin layer, the water-absorbing effect only works on the water-absorbing polymers exposed on the surface, but when mechanical embossing is applied to obtain a decorative design, The exposed area of the water-absorbing polymer that was exposed on the surface became narrow, or in the case of crumpled edges, it was crushed and the original dew condensation prevention effect could not be expected.
また、無数の連通する微細気泡を有する発泡層としたも
のも、意匠性を確保するために機械的エンボス加工を施
すと、エンボス時の加熱で発泡合成樹脂層が溶融して連
通ずる微細気泡が消失したりしたうえ、エンボス時の機
械的圧力により、凹部分の連通ずる微細気泡が押し潰さ
れてしまい、やはり所望する結露防止効果が得られなか
った。In addition, when a foamed layer with countless interconnected microscopic cells is mechanically embossed to ensure the design, the foamed synthetic resin layer melts due to the heating during embossing, creating interconnected microscopic cells. Not only that, but also the mechanical pressure during embossing crushed the communicating microbubbles in the concave portions, so that the desired dew condensation prevention effect could not be obtained.
オレフィン系微多孔シートにより透湿性をもたせたもの
でも、意匠性を得るために、機械的エンボス加工を施す
と、エンボス時の加熱により、シートの微多孔が溶融し
て塞がったり、凹部では微多孔が押し潰されてしまい、
やはり所望の透湿を著しく損なってしまっていた。Even if a microporous olefin sheet is used to provide moisture permeability, if mechanical embossing is applied to create a design, the heating during embossing may melt and close the micropores in the sheet, or the micropores may close in the recesses. was crushed,
After all, the desired moisture permeability was significantly impaired.
パンチング加工による場合にも、エンボス時に穴が塞が
ったり、一般に化学的な微細気泡よりも大きな穴しかあ
けられない為に、意匠性を損ねたり、針布によりもうけ
られた穴に汚れが付着するなどの欠、?!:を有してい
た。Even when punching is used, the holes may become clogged during embossing, the design may be impaired because holes that are generally larger than chemical microbubbles can be made, and dirt may adhere to the holes made by the clothing. Lack of? ! : had.
〈問題点を解決するた、めの手段〉
そこで本発明は、吸水性高分子、連通ずる微細気泡を有
する発泡層、透湿性樹脂という三者三様の長所をもつベ
ースの上に、模様状に形成した音道の発泡合成樹脂とを
組合せることによりきわめて優れた凹凸模様を有する発
泡装飾材の製造方法を提供することをその目的としてな
されたものである。<Means for Solving the Problems> Therefore, the present invention provides a patterned structure on a base that has the three advantages of a water-absorbing polymer, a foam layer having communicating micro-cells, and a moisture-permeable resin. The object of this invention is to provide a method for manufacturing a foamed decorative material having an extremely excellent uneven pattern by combining the foamed synthetic resin with a foamed synthetic resin formed in the same way.
また、従来技術では凹部分と凸部分を比較すると、凹部
分の結露防止効果が劣ることが欠点であったが、本発明
の方法では凹部分の結露防止効果を確保しておき、凸部
分は結露防止機能が無くても、表面温度の差により実質
上、結露しないことに着目して、意匠性を高めながら結
露防止効果を維持する発泡装飾材の製造方法を提供する
ものである。Furthermore, when comparing the concave and convex portions of the conventional technology, the disadvantage was that the concave portions were less effective at preventing condensation, but the method of the present invention ensures the dew condensation prevention effect of the concave portions, and the convex portions are To provide a method for manufacturing a foamed decorative material that maintains a dew condensation prevention effect while improving design, focusing on the fact that even without a dew condensation prevention function, dew condensation does not occur due to the difference in surface temperature.
一般に、壁面に貼られた装飾材の表面に結露が生じるの
は、室内温度と壁面の裏からの伝導熱により壁面に直接
貼られた装飾材の表面温度に大きな差がでた場合である
。Generally, dew condensation occurs on the surface of a decorative material attached to a wall when there is a large difference in the surface temperature of the decorative material directly attached to the wall due to indoor temperature and conductive heat from the back of the wall.
本発明は、紙・布等の基材上に微粉状の吸水性高分子及
び加熱発泡後無数の連通ずる微細気泡を造出する発泡剤
を含有させた第1の発泡性合成樹脂を積層し、必要に応
じて所望の印刷を該第1の発泡性合成樹脂層にしたあと
、その上に透湿性樹脂皮膜を形成し、更にその上に発泡
剤を含有した第2の発泡性合成樹脂を任意の模様状に形
成したのち、前記第1及び第2の発泡性合成樹脂を加熱
発泡させて凹凸模様を現出させる構成としたものである
。以下、さらに詳細に説明すると、基材としては、紙、
布、不織布水酸化アルミニュウム紙などの任意のものが
用いられる。尚、製品の裏面からの透湿性が必要な場合
には、これらの基材も透湿性(代用特性としては通気性
)を有するものを選択すればよく、基材裏面からの透湿
性を必要としない場合には、合成紙あるいはポリエチレ
ン層を中間に設けたポリサンド紙を選択してもよい。The present invention involves laminating a first foamable synthetic resin containing a finely powdered water-absorbing polymer and a foaming agent that creates countless interconnected microscopic cells after heating and foaming on a base material such as paper or cloth. After applying desired printing to the first foamable synthetic resin layer as necessary, a moisture-permeable resin film is formed thereon, and a second foamable synthetic resin containing a foaming agent is further applied thereon. After forming an arbitrary pattern, the first and second foamable synthetic resins are heated and foamed to reveal an uneven pattern. To explain in more detail below, the base materials include paper,
Any material such as cloth, nonwoven aluminum hydroxide paper, etc. can be used. In addition, if moisture permeability from the back side of the product is required, these base materials should also be selected to have moisture permeability (breathability as a substitute characteristic); If not, synthetic paper or polysand paper with a polyethylene layer in between may be selected.
これらの基材の上に、コーティング法、トッピング法、
ラミネーター法、あるいはロータリー法等公知の積層方
法で、微粉状の吸水性高分子及び加熱発泡後無数の連通
ずる微細気泡を造出する発泡剤を含有させた第1の発泡
性合成樹脂層を形成する。On top of these base materials, coating methods, topping methods,
Using a known lamination method such as a laminator method or a rotary method, a first foamable synthetic resin layer containing a finely powdered water-absorbing polymer and a foaming agent that creates countless interconnected microbubbles after heating and foaming is formed. do.
この第1の発泡性合成樹脂層に用いられる樹脂としては
加熱発泡性の塩化ビニル樹脂をはじめとして任意のもの
が使用出来る。As the resin used for this first foamable synthetic resin layer, any resin including heat-foamable vinyl chloride resin can be used.
吸水性高分子は、それ自体は公知の、水を吸収して膨張
することのできる親水性樹脂であり自重の50倍以上の
純水を吸収しつる性能であることが望ましい、主な吸水
性高分子としてはでんぷん/−アクリル酸ソーダグラフ
ト共重合体ビニルエステル/エチレン系不飽和カルボン
酸またはその誘導体の鹸化物、ポリアクリル酸ソーダ架
橋体、ポリビニルアルコール/アクリル酸塩グラフト共
重合体等を、挙げることができる。市販品では例えばス
ミカゲル−8P(住友化学製品)、サンウェットIM−
300(三洋化成製品)、アクアキープ4S(製鉄化学
工業製品)等がある。これらの吸水性高分子は、通常粒
子径350μ〜0.1μ程度の微粉末であるが、分散性
を考慮すると平均粒径100μ以下が好ましい、添加部
数としては、通常2〜40部であるが好ましくは5〜1
5部前後である。The water-absorbing polymer itself is a well-known hydrophilic resin that can absorb water and expand, and it is desirable that it has the ability to absorb 50 times or more of its own weight of pure water. Examples of polymers include starch/sodium acrylate graft copolymer vinyl ester/saponified product of ethylenically unsaturated carboxylic acid or its derivatives, polysodium acrylate crosslinked product, polyvinyl alcohol/acrylate graft copolymer, etc. can be mentioned. Commercial products such as Sumikagel-8P (Sumitomo Chemical) and Sunwet IM-
300 (Sanyo Chemical Products), Aqua Keep 4S (Steel Chemical Industry Products), etc. These water-absorbing polymers are usually fine powders with a particle size of about 350μ to 0.1μ, but in consideration of dispersibility, an average particle size of 100μ or less is preferable.The number of parts added is usually 2 to 40 parts. Preferably 5-1
There are around 5 copies.
上記した第1の発泡性合成樹脂に含有させる発泡剤は、
発泡後の状態で連続気泡率70%以上にするのが結露防
止効果上好ましい。その比率の調整は独立気泡形成の発
泡剤と連続気泡(連通気泡)形成の発泡剤との混合比率
あるいは安定剤の選定による発泡スピードの調整、ある
いは発泡加熱温度と発泡加熱時間の調整等により達成で
きる。前掲の特開昭53−31772号公報には発泡材
(ユニホームAZ−F 入場薬品)と安定剤(スタビ
ライザーF 共同薬品)の組合せ、発泡剤(オニファイ
ンMO入場薬品)と任意の安定剤との組合せの例示があ
るが、本発明の場合にも、これら公知の組合せのものが
利用出来る。塩化ビニル樹脂の場合には通常のアゾシカ
−ボンアマイドが用いられることが多い。The foaming agent contained in the first foamable synthetic resin described above is
It is preferable to have an open cell ratio of 70% or more in the foamed state from the viewpoint of preventing dew condensation. The ratio can be adjusted by adjusting the mixing ratio of the foaming agent for forming closed cells and the foaming agent for forming open cells, adjusting the foaming speed by selecting a stabilizer, or adjusting the foaming heating temperature and foaming heating time. can. The above-mentioned Japanese Patent Application Laid-Open No. 53-31772 describes a combination of a foaming material (Uniform AZ-F, a chemical agent) and a stabilizer (Stabilizer F, Kyodo Yakuhin), and a combination of a foaming agent (Onifine MO, a chemical agent) and an arbitrary stabilizer. Although there are examples of combinations, these known combinations can also be used in the present invention. In the case of vinyl chloride resin, common azosica-bonamide is often used.
透湿性樹脂としては、例えばウレタン系W10型エマル
ジョン樹脂、アミノ酸/メタクリル酸/ウレタン共重合
体のほかに、前記オレフィン系樹脂の微多孔シート等が
掲げられるが、発泡のための高温加熱の際、透湿性樹脂
の性能を失わず、かつまた、壁装剤として用いた場合に
汚れた時に拭きとる際の洗浄汚水の滲み込みをなくすた
め、水蒸気の形態の場合のみ通過させるが、液体の形で
は通過させないアミノ酸/メタクリル酸/ウレタン共重
合体が好ましいが、これと同等の機能をもつほかの透湿
性樹脂でも差し支えない。基材に積層された第1の発泡
性合成樹脂の上に透湿樹脂皮膜を形成するには、透湿性
樹脂塗料をコーティング法により塗布するか、グラビア
印刷機により表面処理して塗布するか、もしくはあらか
じめ形成していた透湿性樹脂フィルムをラミネートして
も良い。Examples of moisture-permeable resins include urethane-based W10 emulsion resins, amino acid/methacrylic acid/urethane copolymers, and microporous sheets of the above-mentioned olefin resins. In order not to lose the performance of the moisture-permeable resin, and also to eliminate the seepage of cleaning waste water when wiping it off when it becomes dirty when used as a wall covering material, it is allowed to pass through only in the form of water vapor, but not in the form of liquid. An amino acid/methacrylic acid/urethane copolymer that does not allow it to pass through is preferred, but other moisture-permeable resins with equivalent functionality may also be used. In order to form a moisture-permeable resin film on the first foamable synthetic resin laminated on the base material, a moisture-permeable resin paint is applied by a coating method, or by surface treatment using a gravure printing machine. Alternatively, a pre-formed moisture-permeable resin film may be laminated.
尚、意匠性をよくする為透湿樹脂皮膜を形成する前に、
必要に応じて、第1の発泡性合成樹脂層上に任意の模様
を印刷することも出来るし透湿性樹脂皮膜の機能を損ね
ないような小さな印刷柄であれば、透湿性樹脂皮膜を形
成したあとに、印刷模様を付与してもよいが、好ましく
は透湿樹脂皮膜形成前のほうがよい。In addition, in order to improve the design, before forming the moisture permeable resin film,
If necessary, any pattern can be printed on the first foamable synthetic resin layer, and if the printed pattern is small enough not to impair the function of the moisture-permeable resin film, the moisture-permeable resin film can be formed. Although a printed pattern may be applied later, it is preferable to do so before forming the moisture-permeable resin film.
さて、基材に第1の発泡性合成樹脂を積層しその上に透
湿性樹脂皮膜を形成したあと、更にその上に、発泡剤を
含有した第2の発泡性合成樹脂を任意の模様状に形成す
るわけであるが、この第2の発泡性合成樹脂には吸水性
高分子及び連通ずる微細気泡を造出する発泡剤を含有さ
せていないので、この第2の発泡性合成樹脂には結露防
止効果は期待出来ないことになる。そこで、この模様状
に形成する第2の発泡性合成樹脂の総合計面積は、第1
の発泡性合成樹脂層の面積の80%以下が好ましく、出
来れば70%位までにとどめることが望ましい、この比
率は模様状に形成する際の意匠により左右されるが、ど
の部分でも平均して、第1の発泡性合成樹脂層が直接露
出しているように配慮した方がよいといえる。この様に
した、基材に第1の発泡性合成樹脂を積層し、その上に
透湿性樹脂皮膜を形成し、更にその上に模様状に第2の
発泡性合成樹脂を形成した状態のものを、発泡加熱炉に
導き発泡加熱処理して、第1および第2の発泡性合成樹
脂を発泡膨出させると、第2の発泡性合成樹脂が模様状
に形成されている部分が曲部分となり、そうでないとこ
ろが開部分となる発泡凹凸模様が現出することになる。Now, after laminating the first foamable synthetic resin on the base material and forming a moisture permeable resin film on it, a second foamable synthetic resin containing a foaming agent is further layered on top of it in an arbitrary pattern. However, since this second foamable synthetic resin does not contain a water-absorbing polymer and a foaming agent that creates communicating microbubbles, there is no condensation in this second foamable synthetic resin. The preventive effect cannot be expected. Therefore, the total area of the second foamable synthetic resin formed in this pattern is
The area of the foamable synthetic resin layer is preferably 80% or less, preferably up to 70%.This ratio depends on the design when forming the pattern, but on average in any part. It can be said that it is better to take care so that the first foamable synthetic resin layer is directly exposed. In this way, the first foamable synthetic resin is laminated on the base material, a moisture-permeable resin film is formed on top of the first foamable synthetic resin, and the second foamable synthetic resin is further formed in a pattern on top of that. When the first and second foamable synthetic resins are foamed and swollen by being guided into a foaming heating furnace and subjected to foaming heat treatment, the patterned portions of the second foamable synthetic resins become curved portions. , a foamed uneven pattern with open areas will appear where this is not the case.
この発泡凹凸模様は、開部分は第1の発泡性合成樹脂が
発泡した部分であるので、連通ずる微細気泡が造出され
ており、しかも吸水性高分子を含有したものとなり、そ
の上には透湿性樹脂皮膜が形成された状態の凹部分とな
る。In this foamed uneven pattern, since the open part is the part where the first foamable synthetic resin is foamed, communicating fine bubbles are created, and moreover, it contains a water-absorbing polymer. This becomes a concave portion with a moisture-permeable resin film formed thereon.
凸部分は凹部分の第1の発泡性合成、m脂層が発泡した
上に、模様状に形成されている第2の発泡性合成樹脂が
発泡したものである。The convex portions are the first foamable synthetic resin of the concave portions, and the second foamable synthetic resin formed in a pattern is foamed in addition to the foamed resin layer.
この様にして製造された凹凸模様を有する発泡装飾材の
結露防止効果をテストしたところ、凸部発泡層の厚みよ
りも、凹部の上の第2の発泡性合成樹脂が発泡した層の
厚みが厚い場合には、凸部分の上部に位置する発泡性合
成樹脂層表面にも結露しにくいことが確認された。When we tested the dew condensation prevention effect of the foamed decorative material with an uneven pattern manufactured in this way, we found that the thickness of the layer formed by the second foamed synthetic resin above the recesses was greater than the thickness of the foam layer of the convexities. It was confirmed that when it is thick, dew condensation is less likely to occur on the surface of the foamable synthetic resin layer located above the convex portion.
これは、壁面に本発明により製造された凹凸模様を有す
る発泡装飾材を貼った場合、壁面裏側からの放熱により
、発泡装飾材の表面温度が左右される際に、凸部発泡層
よりも、凸部発泡層の方が壁面裏側からの放熱が阻害さ
れ、より室温に近い温度となり、結露しにくい状態にあ
るからである。This is because when a foamed decorative material having an uneven pattern manufactured according to the present invention is attached to a wall surface, when the surface temperature of the foamed decorative material is influenced by heat radiation from the back side of the wall surface, the temperature is higher than that of the convex foam layer. This is because the convex foam layer inhibits heat dissipation from the back side of the wall surface, resulting in a temperature closer to room temperature, making it difficult for dew condensation to occur.
さらに詳細に考察すれば、室内の壁面に発泡装飾材を貼
った場合に、壁面が建物の北側に位置したりしていると
外気温が室温より低い場合に、壁面裏側の温度が放熱(
熱伝導)によりどんどん低下していき、それが室内の壁
面に貼られている発泡装飾材の表面温度を室温よりはる
かに低下させる現象をおこして、その時の室内の湿度と
の関係により、壁面に貼られた発泡装飾材の表面に結露
が発生しようとすることになる。Taking a more detailed look, when foam decoration is pasted on an indoor wall, if the wall is located on the north side of the building and the outside temperature is lower than room temperature, the temperature on the back side of the wall will increase due to heat dissipation (
This causes a phenomenon in which the surface temperature of the foam decorative material attached to the indoor wall becomes much lower than room temperature, and due to the relationship with the indoor humidity at that time, Condensation will tend to form on the surface of the applied foam decoration material.
これを透湿性樹脂被膜や吸水性高分子及び無数の連通ず
る微細気泡の作用により、結露現象を防止するわけであ
るが、本発明の方法により製造されたものは凸部分の表
面にはこれらの機能が付与されていないが、基材から白
部分表面までの厚みが、凹部発泡層の厚みよりも厚いこ
とにより、断熱性に冨み、凹部発泡層の表面温度よりも
常に高い表面温度を示すことに本発明者は気がつき、さ
らに凸部の上部発泡層は連通ずる気泡ではなく、独立気
泡による発泡層となっているため、単に凹部の厚みの2
倍の厚みであっても、断熱性能は2倍以上になることを
見つけて、こ、れを積換的に利用することとしたもので
ある。The condensation phenomenon is prevented by the action of a moisture-permeable resin coating, a water-absorbing polymer, and countless communicating microbubbles, but the products manufactured by the method of the present invention do not have these on the surface of the convex parts. Although it has no function, the thickness from the base material to the surface of the white part is thicker than the thickness of the recessed foam layer, so it has rich insulation properties and always shows a higher surface temperature than the surface temperature of the recessed foam layer. The inventor of the present invention noticed that, and furthermore, since the upper foam layer of the convex part is a foam layer made of closed cells rather than continuous cells, it is simply 2 times the thickness of the concave part.
We found that even if the thickness was twice as high, the insulation performance would be more than double, and we decided to utilize this for transshipment purposes.
種々の試験により、凸部発泡厚みと凹部発泡厚みの差が
下記の条件を満たす時に凸部にも通常の室内状態では結
露しないことがわかった。Through various tests, it was found that when the difference between the foamed thickness of the convex portion and the foamed thickness of the concave portion satisfies the following conditions, no condensation occurs on the convex portion under normal indoor conditions.
凸部発泡厚み 〉 四部発泡厚み ×1.5但し、上記
式の凸部発泡厚みは基材面からの厚みであり、第1及び
第2の発泡性合成樹脂層の両方の合計の厚みである。Foaming thickness of the convex portion 〉 Four-part foaming thickness × 1.5 However, the foaming thickness of the convex portion in the above formula is the thickness from the base material surface, and is the total thickness of both the first and second foamable synthetic resin layers. .
この様な条件を満たすには、色々な組合わせが可能であ
る。Various combinations are possible to satisfy these conditions.
まず、発泡剤の発泡倍率が同じである場合には第1の発
泡性合成樹脂の積層厚みよりも、その上に模様状に形成
される第2の発泡性合成樹脂層の塗布厚みを厚くするこ
とにより、発泡加熱処理した後の凸部と凹部の厚みが前
述した式%式%
別な組み合わせとしては、第1の発泡性合成樹脂の積層
厚みと第2の発泡性合成樹脂の塗布(塗着)厚みを同じ
か、あるいは若干、第2の発泡性合成樹脂の塗布厚みを
薄くする場合には発泡剤の選定をすることにより、発泡
可熱処理した後の凸部と凹部の厚みが面述した式にあ、
てはまることになる。First, when the foaming ratio of the foaming agent is the same, the coating thickness of the second foamable synthetic resin layer formed in a pattern thereon is thicker than the laminated thickness of the first foamable synthetic resin. As a result, the thickness of the convex portions and concave portions after the foaming heat treatment can be determined according to the formula % formula % described above. (3) If the thickness of the second foamable synthetic resin is to be the same or slightly thinner, the thickness of the convex and concave parts after the foaming heat treatment can be adjusted by selecting the foaming agent. In the ceremony,
It will fit.
すなわち、第1の発泡性合成樹脂層に含有させる加熱発
泡後無数の連通ずる微細気泡を造出する発泡剤よりも分
解温度が低い発泡剤を第2の発泡性合成樹脂に含有させ
ることにより、第1と第2の発泡性合成樹脂を発泡可熱
処理したときに、同一の発泡加熱時間・発泡加熱時間で
あれば、第2の発泡性合成樹脂層のほうの発泡倍率を高
くさせられることを利用したものである。That is, by making the second foamable synthetic resin contain a foaming agent whose decomposition temperature is lower than that of the foaming agent that is contained in the first foamable synthetic resin layer and which creates countless interconnected microscopic cells after heating and foaming. When the first and second foamable synthetic resins are subjected to foaming heat treatment, if the foaming heating time and foaming heating time are the same, the foaming ratio of the second foamable synthetic resin layer can be increased. It was used.
一般に、発泡剤を使用する合成樹脂発泡法では、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、アジゾ化合物といった有機発泡剤のほか
に無機発泡剤があって、それぞれ分解温度や分解ガス発
生用を異にしていることはよく知られている。In general, in synthetic resin foaming methods that use blowing agents, decomposable blowing agents are widely used as blowing agents, and such decomposable blowing agents include organic blowing agents such as azo compounds, sulfohydrazide compounds, nitroso compounds, and azizo compounds. It is well known that there are other inorganic blowing agents in addition to the above, and each has different decomposition temperatures and decomposition gas generation capabilities.
音道、分解温度は、合成樹脂あるいはその原科、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、例えばアゾシカ−ボンアマイド(ADCA)系
では、その分解温度が約200℃前後であるのに対して
、オキシビスベンゼンスルホニルヒドラジド(OBSH
)系では約130℃前後であるといったように比較的大
きな分解温度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。The sound path and decomposition temperature change greatly when mixed with synthetic resins or their raw materials, plasticizers, solvents, stabilizers, acids, bases, etc., and especially when blowing agents are dissolved in the compounding agent. However, for example, in the case of azosica-bonamide (ADCA), its decomposition temperature is around 200°C, whereas in the case of oxybisbenzenesulfonyl hydrazide (OBSH), its decomposition temperature is around 200°C.
) system, it is easy to select two types of decomposable blowing agents that exhibit relatively high decomposition temperatures, such as around 130°C.
本発明においても、第1の発泡性合成樹脂に含有させる
発泡剤をADCA系にし、第2の発泡性合成樹脂には0
BSH系の発泡剤を含有させれば、曲部分の発泡層の厚
みのは、うが凹部発泡層の厚みの2倍以上とすることが
出来る。Also in the present invention, the foaming agent contained in the first foamable synthetic resin is ADCA type, and the foaming agent contained in the second foamable synthetic resin is 0.
If a BSH-based foaming agent is included, the thickness of the foam layer in the curved portion can be made more than twice the thickness of the foam layer in the gargle recess.
しかも、第1の発泡性合成樹脂の発泡した層は、無数に
連通ずる微細気泡とすることが出来る。又 ただ単純に
、発泡剤の含有量をかえることによる組合わせでも可能
である。Moreover, the foamed layer of the first foamable synthetic resin can be formed into a countless number of communicating fine cells. It is also possible to create combinations simply by changing the content of the blowing agent.
これらの第2の発泡性合成樹脂を任意の模様状に透湿性
樹脂被膜を設けた第1の発泡性合成樹脂の上に塗布(塗
着)するには、ロータリースクリーン印刷機やグラビア
捺染印刷機等の公知のものを使用することが出来る。In order to coat (paint) these second foamable synthetic resins on the first foamable synthetic resin provided with a moisture-permeable resin coating in an arbitrary pattern, a rotary screen printing machine or a gravure textile printing machine is used. It is possible to use known ones such as.
的述した様に、凸部発泡厚み〉凹部発泡厚み×1.5の
場合には5通常の室内の生活条件下では、凸部表面にも
ほとんど結露現象が発生しないが、凸部発泡厚み〉凹部
発泡厚み×2の条件を満たす時にはかなりの過酷な条件
下でも、凸部に結露現象が発生しないことが試験の結果
判明しているが、通常の発泡装飾材として使用する場合
には、凸部発泡厚みを凸部発泡厚みの1.5倍以上、好
ましくは、1.7倍程度に設定することが望ましい。As mentioned above, if the foaming thickness of the convex portion > the foaming thickness of the concave portion x 1.5, 5. Under normal indoor living conditions, condensation hardly occurs on the surface of the convex portion, but the foaming thickness of the convex portion > Tests have shown that when the condition of 2 times the foam thickness in the concave part is satisfied, no condensation occurs on the convex part even under extremely harsh conditions.However, when used as a normal foam decorative material, It is desirable to set the foaming thickness of the part to 1.5 times or more, preferably about 1.7 times, the foaming thickness of the convex part.
〈発明の効果〉
本発明の方法によれば、第1の発泡性合成樹脂層が発泡
してなる凹部分は、連通ずる微細気泡を有する発泡性合
成樹脂層であり、しかもその発泡層には微粉末状の吸水
性高分子がほぼ均一に混入散在しており、しかもその発
泡合成樹脂層の表面は透湿性樹脂皮膜層が形成されてい
る。<Effects of the Invention> According to the method of the present invention, the concave portion formed by foaming the first foamable synthetic resin layer is a foamable synthetic resin layer having communicating fine cells, and furthermore, the foamed layer contains The water-absorbing polymer in the form of fine powder is almost uniformly mixed and scattered, and a moisture-permeable resin film layer is formed on the surface of the foamed synthetic resin layer.
従って、凹部表面に結露が生じようしても、その湿気は
透湿性樹脂皮膜層を通過して発泡合成樹脂層の連続微細
気泡及び吸水性高分子により積掻的に吸収されるため、
開部分表面に結露の発生を生じさせることがない。Therefore, even if dew condensation occurs on the surface of the recess, the moisture will pass through the moisture-permeable resin film layer and be absorbed by the continuous fine cells of the foamed synthetic resin layer and the water-absorbing polymer.
There is no possibility of condensation forming on the surface of the open part.
また、第2の発泡性合成樹脂が発泡した凹部の下層には
第1の発泡性合成樹脂が発泡した状態で存在しており、
凸部面からの吸湿はないが凹部分が直接表面になってい
る部分からの吸湿された水分が横方向に拡散して凸部の
下層に位置する第1の発泡性合成樹脂が発泡した発泡層
も、実質上は結露防止効果を補強することになる。Further, the first foamable synthetic resin is present in a foamed state in the lower layer of the recess where the second foamable synthetic resin is foamed,
There is no moisture absorption from the surface of the convex part, but the moisture absorbed from the part where the concave part is the direct surface is diffused laterally, and the first foamable synthetic resin located below the convex part foams. The layer will also substantially reinforce the anti-condensation effect.
また第1の発泡性合成樹脂が発泡した層は機械的エンボ
ス加工を全く施されないので、連通ずる無数の微細気泡
や吸水性高分子の吸効果が損なわれることがない。Furthermore, since the layer in which the first foamable synthetic resin is foamed is not mechanically embossed at all, the countless interconnected microscopic cells and the absorption effect of the water-absorbing polymer are not impaired.
また第2の発泡性合成樹脂が模様状に第1の発泡性合成
樹脂層の上に形成されるわけであるが、透湿樹脂皮膜を
施された第1の発泡性合成樹脂層が直接露出する凹部発
泡層の面積が20〜30%程度でも発泡装飾材全体の吸
湿効果は低下しないという優れた効果をもつものである
。In addition, the second foamable synthetic resin is formed in a pattern on the first foamable synthetic resin layer, but the first foamable synthetic resin layer coated with a moisture-permeable resin film is directly exposed. Even if the area of the concave foamed layer is about 20 to 30%, the moisture absorption effect of the entire foamed decorative material does not decrease, which is an excellent effect.
また、第2の発泡性合成樹脂が発泡して凸部発泡層を形
成すること1こなるのであるが第2の発泡性合成樹脂が
発泡した部分は独立気泡による発泡層であり、凹部に比
較して断熱効果が格段に優れている。この為、前述した
発泡厚みの式を満たすように設定しておけば、凹部発泡
層の表面温度よりも、凸部発泡層の表面温度のほうが、
常に室温に近く、同一の室内湿度条件下では、凸部発泡
層表面には結露が生じることはなく、凹部発泡層が積掻
的に吸湿していくことになる。しかも直接表面に露出し
ている凹部発゛泡層の面積比率が凸部発泡層の面積より
も小さくても、前記したように、凸部の下層に存在する
第1の発泡性合成樹脂が発泡した合成樹脂部分も吸湿(
吸水)体と−して機能するので、従来のものに比べて、
結露防止効果が優れているものである。In addition, the second foamable synthetic resin foams to form a convex foam layer, but the foamed part of the second foamable synthetic resin is a foam layer made of closed cells, and compared to the concave portion. It has an extremely good insulation effect. Therefore, if the foam thickness is set to satisfy the formula for the foam thickness mentioned above, the surface temperature of the convex foam layer will be higher than that of the concave foam layer.
Under the same indoor humidity conditions that are always close to room temperature, no dew condensation occurs on the surface of the convex foam layer, and the concave foam layer absorbs moisture cumulatively. Moreover, even if the area ratio of the foam layer in the concave portions directly exposed to the surface is smaller than the area of the foam layer in the convex portions, as described above, the first foamable synthetic resin present in the layer below the convex portions is foamed. The synthetic resin part also absorbs moisture (
Since it functions as a water absorbing body, compared to conventional ones,
It has an excellent dew condensation prevention effect.
また、従来技術による結露防止装飾材に比較すると、凹
部も凸部も発泡層で形成されているので、見た目の意匠
性も暖かく柔らかい感じがする点でも甚だ優れたもので
ある。Furthermore, compared to conventional dew condensation prevention decorative materials, since both the concave and convex portions are formed of a foam layer, the decorative material is extremely superior in terms of appearance and warm and soft feel.
く 実施例 〉
壁紙用の難燃紙lに下記配合よりなる第1の発泡性塩化
ビニル樹脂ペーストをドクターナイフコート法により、
0.1511++m厚に塗布積層し、これを発泡剤の分
解温度よりも低い温度で乾燥半ゲル化させて、第1の発
泡性合成樹脂層2を作成した(第1−A図)。Example 〉 A first foamable vinyl chloride resin paste consisting of the following formulation was applied to flame-retardant paper for wallpaper using a doctor knife coating method.
The first foamable synthetic resin layer 2 was prepared by coating and laminating to a thickness of 0.1511++ m and drying and semi-gelling at a temperature lower than the decomposition temperature of the foaming agent (Figure 1-A).
樹 脂・−一ボリ塩化ビニル樹脂 !00 部可塑
剤−−DOP 50 glS安定
剤−−−B a −Z n系 3 都発泡剤
−−−−A D CA系 5 部吸水性高
分子−−スミ力ゲル
5P−52010部
充填剤・−一炭酸カルシウム 50 部顔 科
−・・−チタン白 15 部防カビ剤・
・・・・・ビオサイド 2.5部次に上記第
1の発泡性合成樹脂層2の上に、クラビア印刷機を使用
し、アミノ酸/メタクリル酸/ウレタン共重合体からな
る透湿性樹脂塗料を塗布乾燥することで、透湿性樹脂皮
膜層3を形成した(第1−B図)。Resin: Monopolyvinyl chloride resin! 00 parts Plasticizer --- DOP 50 glS Stabilizer --- B a -Z n system 3 Miyako foaming agent --- AD CA system 5 parts Water-absorbing polymer -- Sumiriki Gel 5P-520 10 parts Filler. - Calcium monocarbonate 50 parts Face - Titanium white 15 parts Antifungal agent
...Biocide 2.5 parts Next, on top of the first foamable synthetic resin layer 2, a moisture permeable resin paint consisting of an amino acid/methacrylic acid/urethane copolymer is applied using a Clavia printing machine. By drying, a moisture permeable resin film layer 3 was formed (Figure 1-B).
つづいて、透湿性樹脂皮膜層3の上に、ロータリースク
リーン印刷機を使用して下記配合の第2の発泡性塩化ビ
ニル樹脂ペーストを亀甲模様に0.19mm厚に塗布し
て、発泡剤の分解温度よりも低い温度で乾燥半ゲル化さ
せて、第2の発泡性合成樹脂4を形成した(第1−C図
)。この亀甲模様状に形成された第2の発泡性合成樹脂
層4の面積比率は総合計でほぼ60%程度であり、約4
0%は透湿性樹脂皮膜層3を施された第1の発泡性合成
樹脂層2が直接表面から見えるものであった。Next, on the moisture-permeable resin film layer 3, a second foamable vinyl chloride resin paste having the following composition was applied to a thickness of 0.19 mm in a hexagonal pattern using a rotary screen printing machine to decompose the foaming agent. The second foamable synthetic resin 4 was formed by drying and semi-gelling at a temperature lower than that temperature (Fig. 1-C). The area ratio of the second foamable synthetic resin layer 4 formed in a tortoiseshell pattern is about 60% in total, which is about 4%.
At 0%, the first foamable synthetic resin layer 2 coated with the moisture-permeable resin film layer 3 was directly visible from the surface.
樹 脂・・・・−ポリ塩化ビニル樹脂 100 部
可塑剤−−DOP 50 部安定
剤−o=Ba−Z、n系 3 部発泡剤−−
−−OB S H系 lO部充填剤−−炭
酸カルシウム 20 部顔 料・−一チタン
白 lO部着色剤・−・−青色着色剤
5 部防カビ剤−−ビオサイド
1.5部さらにこれを約230℃に設定された発泡
加熱炉に導き、1分間加熱して、第1及び第2の発泡性
塩化ビニル樹脂層を発泡させたところ、第1の塩化ビニ
ル樹脂層は発泡して約1.2mmの厚みの発泡性合成樹
脂層5を形成し、第2の塩化ビニル樹脂層は発泡して約
1.5mm厚みの亀甲模様状の発泡層6を形成した(第
1−D図)。Resin...-Polyvinyl chloride resin 100 parts Plasticizer--DOP 50 parts Stabilizer-o=Ba-Z, n-based 3 parts Foaming agent--
--OB S H-based 1O part filler--Calcium carbonate 20 parts Pigment--Titanium white 1O part Colorant--Blue coloring agent
Part 5 Antifungal agent -- Biocide
1.5 parts This was further introduced into a foaming heating furnace set at about 230°C and heated for 1 minute to foam the first and second foamable vinyl chloride resin layers. The layers were foamed to form a foamable synthetic resin layer 5 with a thickness of about 1.2 mm, and the second vinyl chloride resin layer was foamed to form a foamed layer 6 in a tortoiseshell pattern with a thickness of about 1.5 mm ( Figure 1-D).
この第1−D図かられかるように、凹部は第1の塩化ビ
ニル樹脂2が発泡した層5の上に透湿性樹脂皮膜が施さ
れているもので、その凹部の厚みは発泡層5だけで約1
.2mmであり、凸部を形成する部分は第1の塩化ビニ
ル樹脂が発泡した発泡層5の上の透湿性樹脂皮膜3の上
にさらに第2の塩化ビニル樹脂4が発泡した発泡層6が
約1.5mmの厚みに形成されているものであり、画部
分の発泡層厚みは合計して約2.7mmにもなり、凸部
発泡厚みは凹部発泡厚みのほぼ2倍以上になり、前述し
た式を満たすものであった。As can be seen from this Figure 1-D, the recessed portion is formed by applying a moisture permeable resin film on the layer 5 made of the first polyvinyl chloride resin 2 foamed, and the thickness of the recessed portion is only the foamed layer 5. about 1
.. 2 mm, and the portion forming the convex portion is a foamed layer 6 made of a second polyvinyl chloride resin 4 foamed on top of the moisture-permeable resin film 3 on the foamed layer 5 made of the first polyvinyl chloride resin foamed. It is formed to a thickness of 1.5 mm, and the total thickness of the foam layer in the image area is about 2.7 mm, and the foam thickness in the convex part is more than twice the foam thickness in the concave part, and as mentioned above. The formula was satisfied.
この凹凸模様を有する結露防止発泡装飾材は凹部・凸部
ともに発泡しており、しかもその断面から、第1の発泡
性合成樹脂2が発泡した発泡層5部分には、無数の連通
ずる微細気泡が造出されていて、吸水性高分子が均一に
混入されているものであり、結露防止効果を充分に発揮
するものであり、意匠的にも大きな凹凸段差が現出され
ており、壁紙として優れたものであった。This condensation-preventing foam decorative material having an uneven pattern is foamed in both the concave and convex portions, and furthermore, from its cross section, the foam layer 5 portion where the first foamable synthetic resin 2 is foamed has countless interconnected fine cells. It has been created with a water-absorbing polymer evenly mixed in, and has a sufficient effect of preventing condensation.It also has a design with large uneven steps, making it suitable for use as wallpaper. It was excellent.
この実施例のものと類似の凹凸模様を有する従来技術に
よる壁紙とを比較検討した試験結果を第1表に示す。Table 1 shows the test results of a comparison between this example and a conventional wallpaper having a similar uneven pattern.
第1表 類似した模様の機械的エンボス加工を施したもの。Table 1 Mechanically embossed with a similar pattern.
比較例B・・・無数の連通ずる微細気泡を有する発泡合
成樹脂層に本実施例の亀甲模様に類似した模様の機械的
エンボス加工を施したもの。Comparative Example B: A foamed synthetic resin layer having countless interconnected microscopic cells was mechanically embossed with a pattern similar to the tortoiseshell pattern of this example.
比較例C−・・非発泡合成樹脂層にオレフィン系微多孔
シートを貼合せて、本実施例の亀甲模様に類似した機械
的エンボス加工を施したもの。Comparative Example C--An olefin microporous sheet was laminated to a non-foamed synthetic resin layer and mechanically embossed similar to the tortoiseshell pattern of this example.
第1表かられかるように、本発明の方法による実施例の
ものは、凸部分のほぼ上半分は普通の発泡層であり、連
通気泡もなく、吸水性高分子も含有していないものであ
るが、断熱性がよいことから、壁紙を貼合わせた面(壁
紙裏面)の温度の影響が緩和され、室温の影響で凸部分
よりも、3℃高いことが確認され、試験条件下では結露
は発生しなかった。As can be seen from Table 1, in the examples obtained by the method of the present invention, almost the upper half of the convex portion was a normal foam layer, and there were no open cells and no water-absorbing polymer was contained. However, due to its good insulation properties, the effect of the temperature on the surface where the wallpaper is pasted (the back side of the wallpaper) is alleviated, and it was confirmed that the temperature was 3℃ higher than the convex part due to the influence of room temperature, and under the test conditions, there was no condensation. did not occur.
第1−A図〜第1−D図は本発明の製造方法による実施
例のそれぞれ異なる段階の態様を説明する為の断面図で
ある。
l・−一・難燃紙(基材)、2−−−−−吸水性高分子
及び連通ずる微細気泡を造出する発泡剤を含有する第1
の発泡性合成樹脂層、3−−−−−透湿性樹脂皮膜、4
−−−−−発泡剤を含有する第2の発泡性合成樹脂層、
5−−−−−第1の発泡性合成樹脂層2の発泡済み合成
樹脂層、6−−−−−−第2の発泡性合成樹脂層4の発
泡済み合成樹脂層。1-A to 1-D are cross-sectional views for explaining aspects of different stages of the embodiment according to the manufacturing method of the present invention. 1.--1. Flame-retardant paper (base material), 2.-- A first containing a water-absorbing polymer and a blowing agent that creates communicating micro-cells.
foamable synthetic resin layer, 3 - moisture permeable resin film, 4
----Second foamable synthetic resin layer containing a foaming agent,
5-----The foamed synthetic resin layer of the first foamable synthetic resin layer 2, 6-----The foamed synthetic resin layer of the second foamable synthetic resin layer 4.
Claims (1)
の連通する微細気泡を造出する発泡剤を含有させた第1
の発泡性合成樹脂を積層し、該第1の発泡性合成樹脂上
に透湿性樹脂被膜を形成した後、更にその上に発泡剤を
含有した第2の発泡性合成樹脂を任意の模様上に形成し
、次に前記した第1及び第2の発泡性合成樹脂を発泡加
熱することを特徴とする凸凹模様を有する結露防止発泡
装飾材の製造方法。1. A first material containing a finely powdered water-absorbing polymer and a foaming agent that creates countless interconnected micro-cells after heating and foaming on the base material.
After laminating the foamable synthetic resins and forming a moisture-permeable resin film on the first foamable synthetic resin, a second foamable synthetic resin containing a foaming agent is further applied on top of it in an arbitrary pattern. 1. A method for producing a condensation-preventing foam decorative material having a concave-convex pattern, the method comprising: forming a condensation-preventing foam decorative material, and then foaming and heating the above-described first and second foamable synthetic resins.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62255293A JPH0197632A (en) | 1987-10-09 | 1987-10-09 | Manufacture of dewing preventive foaming decorative material with embossed pattern |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62255293A JPH0197632A (en) | 1987-10-09 | 1987-10-09 | Manufacture of dewing preventive foaming decorative material with embossed pattern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0197632A true JPH0197632A (en) | 1989-04-17 |
Family
ID=17276751
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62255293A Pending JPH0197632A (en) | 1987-10-09 | 1987-10-09 | Manufacture of dewing preventive foaming decorative material with embossed pattern |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0197632A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10280688A (en) * | 1997-04-10 | 1998-10-20 | Toppan Printing Co Ltd | Curing sheet for hydrated cured body |
| JP2017518796A (en) * | 2014-05-13 | 2017-07-13 | コーニンクレッカ フィリップス エヌ ヴェKoninklijke Philips N.V. | Steaming device parts and steaming devices |
| JP2024532683A (en) * | 2022-07-12 | 2024-09-10 | エルジー・ケム・リミテッド | Composite insulation material containing a layer of superabsorbent polymer |
-
1987
- 1987-10-09 JP JP62255293A patent/JPH0197632A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10280688A (en) * | 1997-04-10 | 1998-10-20 | Toppan Printing Co Ltd | Curing sheet for hydrated cured body |
| JP2017518796A (en) * | 2014-05-13 | 2017-07-13 | コーニンクレッカ フィリップス エヌ ヴェKoninklijke Philips N.V. | Steaming device parts and steaming devices |
| JP2024532683A (en) * | 2022-07-12 | 2024-09-10 | エルジー・ケム・リミテッド | Composite insulation material containing a layer of superabsorbent polymer |
| US12605918B2 (en) | 2022-07-12 | 2026-04-21 | Lg Chem, Ltd. | Composite insulating material comprising super absorbent polymer layer |
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