JPS6081378A - Vinyl wall material for preventing condensation - Google Patents
Vinyl wall material for preventing condensationInfo
- Publication number
- JPS6081378A JPS6081378A JP58189023A JP18902383A JPS6081378A JP S6081378 A JPS6081378 A JP S6081378A JP 58189023 A JP58189023 A JP 58189023A JP 18902383 A JP18902383 A JP 18902383A JP S6081378 A JPS6081378 A JP S6081378A
- Authority
- JP
- Japan
- Prior art keywords
- water
- vinyl
- wall material
- vinyl chloride
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 title claims description 79
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 title claims description 33
- 238000009833 condensation Methods 0.000 title claims description 32
- 230000005494 condensation Effects 0.000 title claims description 32
- 229920002554 vinyl polymer Polymers 0.000 title claims description 31
- 229920005989 resin Polymers 0.000 claims abstract description 41
- 239000011347 resin Substances 0.000 claims abstract description 41
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 38
- 229920001577 copolymer Polymers 0.000 claims abstract description 10
- 239000004014 plasticizer Substances 0.000 claims abstract description 9
- 239000011342 resin composition Substances 0.000 claims abstract description 6
- 229920001567 vinyl ester resin Polymers 0.000 claims abstract description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 4
- 239000006260 foam Substances 0.000 claims description 28
- 229920000247 superabsorbent polymer Polymers 0.000 claims description 19
- 150000003839 salts Chemical class 0.000 claims description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 239000005518 polymer electrolyte Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 28
- 239000000758 substrate Substances 0.000 abstract description 16
- 229920000642 polymer Polymers 0.000 abstract description 7
- 239000004744 fabric Substances 0.000 abstract description 6
- 239000002245 particle Substances 0.000 abstract description 6
- 230000037303 wrinkles Effects 0.000 abstract description 4
- 150000001734 carboxylic acid salts Chemical class 0.000 abstract description 2
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 229920000867 polyelectrolyte Polymers 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 239000000123 paper Substances 0.000 description 11
- -1 carboxylate salt Chemical class 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 238000005187 foaming Methods 0.000 description 5
- 239000004604 Blowing Agent Substances 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 229920001944 Plastisol Polymers 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000004088 foaming agent Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000003292 glue Substances 0.000 description 4
- 239000004745 nonwoven fabric Substances 0.000 description 4
- 239000004999 plastisol Substances 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 238000003672 processing method Methods 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 239000012752 auxiliary agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229920006037 cross link polymer Polymers 0.000 description 3
- 238000004049 embossing Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000001099 ammonium carbonate Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 238000000059 patterning Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000007665 sagging Methods 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- VCGRFBXVSFAGGA-UHFFFAOYSA-N (1,1-dioxo-1,4-thiazinan-4-yl)-[6-[[3-(4-fluorophenyl)-5-methyl-1,2-oxazol-4-yl]methoxy]pyridin-3-yl]methanone Chemical compound CC=1ON=C(C=2C=CC(F)=CC=2)C=1COC(N=C1)=CC=C1C(=O)N1CCS(=O)(=O)CC1 VCGRFBXVSFAGGA-UHFFFAOYSA-N 0.000 description 1
- YEVQZPWSVWZAOB-UHFFFAOYSA-N 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(I)C(CBr)=C1 YEVQZPWSVWZAOB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 108091006629 SLC13A2 Proteins 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 210000003323 beak Anatomy 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004583 superabsorbent polymers (SAPs) Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- WTLBZVNBAKMVDP-UHFFFAOYSA-N tris(2-butoxyethyl) phosphate Chemical compound CCCCOCCOP(=O)(OCCOCCCC)OCCOCCCC WTLBZVNBAKMVDP-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/10—Internal combustion engine [ICE] based vehicles
- Y02T10/12—Improving ICE efficiencies
Landscapes
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】 本発明は、結露防止用ビニル壁材に関する。[Detailed description of the invention] The present invention relates to a vinyl wall material for preventing dew condensation.
更に詳細には、結露による水滴発生の防止と、防カヒ性
を有するビニル壁材を提供することにある。壁紙、天井
表装制などの内装材の多くは、紙、布、不織布なとの基
体に樹脂加工したものや、プラスチックシートそのもの
を加工したものなどが用いられている。例えば、紙又は
布あるいは不織布に塩化ビニル樹脂を加工してなる壁材
は、引張り、引裂などの強度が強くまた、耐水性なども
あり、汚れを容易に払き落せるなどの利点を有すること
から、現在では居間などめほかに、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濡W差−あ
るいは室温の急変や、湿度の変化によって、壁材の表面
に水分が結露し、水滴となってあられれるという欠点を
有している。このように水分が表面に結露すると、シミ
として残ったり、かびが生えるという問題が生ずる。ま
たとくに住居の押入れの壁で結露するとふとんなどがし
めって不快であり、不衛生である。More specifically, it is an object of the present invention to provide a vinyl wall material that prevents the generation of water droplets due to dew condensation and has anti-scratch properties. Many interior materials, such as wallpaper and ceiling coverings, are made of paper, cloth, or non-woven fabrics processed with resin, or processed plastic sheets themselves. For example, wall materials made by processing paper, cloth, or non-woven fabric with vinyl chloride resin have strong tensile and tear strength, are water resistant, and have the advantage of being easy to wipe off dirt. Since then, it is now used not only in living rooms, but also in closets, kitchens, and toilets. However, because this wall material has poor hygroscopicity, water can condense on the surface of the wall material and form water droplets due to a large wettability difference between indoors and outdoors, or sudden changes in room temperature or humidity. It has the disadvantage of being When moisture condenses on the surface, problems such as stains and mold growth occur. In addition, condensation on the walls of a closet in a residence can cause futons to become damp, making it uncomfortable and unsanitary.
このような紙又は布あるい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方法としてすでに高
吸水性高分子と、塩化ビニル樹脂、可塑剤、発泡剤から
なるペーストツルを紙に塗布しtこ後、加熱することに
より発泡させた発泡紙が、高い吸水性と保水性とを有す
ることを見い出し、この発泡紙を結露防止用壁材として
使用することを提案した(特開昭56−88082号公
報)。As a way to improve the drawbacks of wall materials made by processing paper, cloth, or non-woven fabric with vinyl chloride resin, we have already applied paste vines made of super absorbent polymer, vinyl chloride resin, plasticizer, and foaming agent to paper. It was discovered that foamed paper, which was foamed by heating after coating, had high water absorption and water retention properties, and proposed the use of this foamed paper as a wall material to prevent condensation. 56-88082).
しかし、上記の壁材は、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、裏打の基体や
壁材を貼付けるために使用した糊材に移行し、その部分
の基体が伸びて−きれいに貼った壁材面にたるみやしわ
が出来たり、糊材にかびが生えたり、腐ったりして劣化
するという不都合を有している。However, although the above wall materials are 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 materials, and This has the disadvantage that the base material stretches, causing sagging or wrinkles on the surface of the wall material that has been neatly pasted, and that the glue material grows mold or rots and deteriorates.
本発明者は上述の実情に鑑み、結露による水滴の発生を
防止する塩化ビニル壁材について鋭意検討した結果、高
吸水性高分子を含有する塩化ビニル樹脂を主体とする発
泡層と基体との間に、水不透過層を設け1こ本発明の壁
材は基体の伸びによるしわや、糊材のかびの発生がなく
、長期間使用してもたるみゃ壁素材からの剥離を生じな
いことを見い出し本発明を完成するに至つTこ。In view of the above-mentioned circumstances, the inventors of the present invention have conducted extensive studies on vinyl chloride wall materials that prevent the generation of water droplets due to dew condensation, and have found that the gap between the foam layer, which is mainly made of vinyl chloride resin containing a superabsorbent polymer, and the substrate. A water-impermeable layer is provided on the wall material of the present invention.1 The wall material of the present invention does not wrinkle due to the stretching of the base material, does not develop mold on the adhesive material, and does not peel off from the wall material even if used for a long period of time. Heading: The present invention was completed.
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、可塑剤およびその他の補助剤か
らなる樹脂組成物発泡体と、それを被覆した基体よりな
る結露防止用ビニル壁材において、発泡層と基体との間
に水不透過層を設けたことを特徴とする結露防止用ビニ
ル壁材を提供するにある。That is, the present invention relates to a resin composition foam made of a synthetic resin mainly composed of vinyl chloride resin, a superabsorbent polymer, a plasticizer, and other auxiliary agents, and a vinyl wall for preventing condensation made of a base coated with the foam. It is an object of the present invention to provide a vinyl wall material for preventing dew condensation, which is characterized in that a water-impermeable layer is provided between a foam layer and a substrate.
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、それ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。従って結露は未然に防止される。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 that comes into contact with it and the water vapor in the air becomes condensed water, It is quickly absorbed into the resin and retained within the super absorbent polymer. Therefore, dew condensation is prevented.
樹脂層が舅塙#キ呪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、結露防止効果が優れている。Since the resin layer is made of foam, condensed water is absorbed into the resin very quickly, and the condensation prevention effect is excellent.
更+1発明のビニル壁材は、発泡層と基体の間に水不透
過層を設けであるため吸水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越さな
い。Furthermore, since the vinyl wall material of the invention has a water-impermeable layer between the foam layer and the base material, absorbed water does not penetrate into the base material, and the elongation of the base material and the deterioration of the glue material due to moisture are virtually eliminated. do not have.
従って本発明の壁材は、それを壁面に貼って使用した場
合きれいに貼つ1こ状態が畏期間保tこれるという利点
がある。Therefore, the wall material of the present invention has the advantage that when used by pasting it on a wall surface, it can remain in a neatly pasted state for a long period of time.
本発明のビニル壁材の樹脂組成物発泡体に使用される高
吸水性高分子は水を吸収して数倍から千数百倍に膨潤し
て、保水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。しかし、吸水量が自重の80倍以下にな
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
高分子の量が多量になり、ビニル壁材の引張り、引裂等
の機械強度の低下が起こるので、使用する高吸水性高分
子の吸水量は30倍以上のものである方が好ましい。形
状、粒子径についても特に限定はないが、ビニル壁材の
加工性および物性等の面からみると粒子径は出来るだけ
細かいほうが望ましく、平均粒径が100μ以下、好ま
しくは50μ以下のものが良い。The superabsorbent polymer used in the resin composition foam of the vinyl wall material of the present invention absorbs water and swells from several times to several thousand times, retaining water but not dissolving in water. It can be anything. However, when the amount of water absorbed is less than 80 times its own weight, the amount of superabsorbent polymer added to absorb the condensed water becomes large, causing a decrease in mechanical strength such as tension and tearing of the vinyl wall material. It is preferable that the water absorption amount of the superabsorbent polymer used is 30 times or more. There are no particular limitations on the shape or particle size, but from the viewpoint of processability and physical properties of vinyl wall materials, it is desirable that the particle size be as fine as possible, and the average particle size should be 100μ or less, preferably 50μ or less. .
本発明の高吸水性高分子としては、γことえば澱粉とア
クリロニトリルのグラフト共重合体のケン化物、澱粉と
アクリル酸(塩)ダラト共重合体、スチレンと無水マレ
イン酸の共重合体の塩、イソブチレンと無水マレイン酸
共重体の塩の架橋体、アクリル酸および/またはアクリ
ル酸塩の架橋重合体(例えば、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、あるいは重合体の後
架橋物など)、ポリビニルアルコールと無水マレイン酸
の反応物の塩、ポリビニルアルコールとアクリル酸(塩
〕のグラフト共重合体、ビニルエステルとエチレン系不
飽和カルボン酸塩たはその誘導体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ホン酸ま1こはその
誘導体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2架橋体、カルボキシメ
ヂ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、ポリアクリルニl−リルの
ケン化物およびそれらの混合物なと公知の高吸水性高分
子が挙げられる。なかでも架橋構造を有するカルボン酸
塩を含む高分子′電解室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ているので、こ
れを用いることが望ましい。特にビニルエステル<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ろ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
性が良く、該高教性高分子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1こって持続するので、好
ましい。この高吸水性高分子の添加量は塩化ビニル樹脂
100部に対して1部から200部の範囲である。高吸
水性高分子の添加量が1部未満の場合吸湿性が少いため
に結露現象を充分に防止することが出来す、才だ添加量
が200部以上では、壁材としての強度に欠けろ。その
ため前記範囲で使用されるが、好ましくは5部から15
0部の範囲で用いられる。Examples of the superabsorbent polymer of the present invention include γ, a saponified product of a graft copolymer of starch and acrylonitrile, a dalat copolymer of starch and acrylic acid (salt), a salt of a copolymer of styrene and maleic anhydride, A crosslinked product of a salt of isobutylene and maleic anhydride copolymer, a crosslinked polymer of acrylic acid and/or an acrylate (e.g., a self-crosslinked polymer, a crosslinked polymer obtained by polymerization in the coexistence of a crosslinking agent, or a post-polymer polymer) cross-linked products), salts of reaction products of polyvinyl alcohol and maleic anhydride, graft copolymers of polyvinyl alcohol and acrylic acid (salts), copolymers of vinyl esters and ethylenically unsaturated carboxylic acid salts or their derivatives. Saponified products, saponified products of copolymers of vinyl esters and unsaturated polycarphonic acids or their derivatives, polyvinyl alcohol crosslinked products, polyethylene glycol 2 crosslinked products, carboxymethylcellulose crosslinked products, polyvinylpyrrolidone crosslinked products,
Known super absorbent polymers include crosslinked polyacrylamide, saponified polyacrylonyl-lyl, and mixtures thereof. Among them, it is desirable to use a superabsorbent polymer made of a polymer electrolytic chamber containing a carboxylate salt having a crosslinked structure because it has a high water absorption capacity and excellent strength after water absorption. Especially vinyl ester <X)
and ethylenically unsaturated carboxylic acid or its derivative (Y)
The saponified copolymer, which is mainly composed of This is preferable because the dew condensation prevention effect of the dew condensation prevention wall material using the highly conductive polymer is maintained for a long period of time. The amount of the super absorbent polymer added is in the range of 1 part to 200 parts per 100 parts of the vinyl chloride resin. If the amount of superabsorbent polymer added is less than 1 part, the moisture absorption is low and dew condensation can be sufficiently prevented. If the amount added is more than 200 parts, the strength as a wall material will be lacking. . Therefore, it is used within the above range, preferably from 5 parts to 15 parts.
Used in the range of 0 parts.
本発明のビニル壁材の樹脂組成物発泡体として使用され
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懸濁1合や乳化重合な
どの重合方法で得られた一般に使用されているもので良
く、特に制限はない。さらに種々の垂嘴改質剤例えばP
MMA、MB8.、ABS、EVAなどの他の樹脂を添
加してもよい。The vinyl chloride resin used as the resin composition foam for the vinyl wall material of the present invention is a vinyl chloride polymer, a vinyl chloride copolymer, or a mixture thereof, and is obtained by a polymerization method such as suspension polymerization or emulsion polymerization. Any commonly used material may be used, and there are no particular limitations. Furthermore, various beak modifiers such as P
MMA, MB8. , ABS, EVA, etc. may also be added.
塩化ビニル樹脂に添加される可塑剤は、通常のものが用
いられるが、難燃化のためには有機燐酸系の可塑剤を併
用することが望才しい。これらの可塑剤としては、フタ
ル酸ジオクチル等、フタル酸エステル類、アジピン酸2
−エチルヘキシル、セパチン酸ジオクチル等脂肪酸二塩
基エステル類、エポキシ化大豆油、エポキシ化アマニ油
、エポキシへキサヒドロフクル酸ジオクチル等エポキシ
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)、コ
エチレンフタリルグリ11・−ル等2価アルコールエス
テル類、塩素化パラフィン等である。また有機燐酸系可
塑剤の例としては燐酸トリクレジル、燐酸クレジルフェ
ニン久燐酸モノオクチルジフェニル、燐酸トリオクチル
、燐酸トリフェニル、燐酸トリブトキシエチル、燐酸ト
リフチルなどが挙げられる。可塑剤の使用量は、塩化ビ
ニル樹脂100部に対して、30部から150部の範囲
であり、この範囲内において目的に応じ、任意の割合を
とることが出来る。さらに、本発明のビニル壁利を構成
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
に応じて添加される。その添加割合は所望する製品によ
り変えられる。このような補助剤は、具体的には安定剤
、炭カル、クレーなどの無機充填剤、顔料、希釈剤、難
燃剤、防カビ剤などである。Although ordinary plasticizers are used to add vinyl chloride resin, it is preferable to use an organic phosphoric acid plasticizer in combination for flame retardancy. These plasticizers include dioctyl phthalate, phthalate esters, adipic acid 2
- Fatty acid dibasic esters such as ethylhexyl and dioctyl sepatate, epoxidized soybean oil, epoxidized linseed oil, epoxides such as dioctyl epoxy hexahydrofucrate, poly(propylene adipate), poly(1,3-butylene sebacate), coethylene These include dihydric alcohol esters such as phthalylglyl-11-ol, chlorinated paraffin, and the like. Examples of organic phosphoric acid plasticizers include tricresyl phosphate, cresyl phenyl phosphate, monooctyldiphenyl phosphate, trioctyl phosphate, triphenyl phosphate, tributoxyethyl phosphate, and triphthyl phosphate. The amount of plasticizer used is in the range of 30 to 150 parts per 100 parts of vinyl chloride resin, and any proportion within this range can be used depending on the purpose. Furthermore, commonly used adjuvants may be added to the vinyl chloride resin constituting the vinyl wall resin of the present invention, if necessary. The addition ratio can be varied depending on the desired product. Examples of such auxiliary agents include stabilizers, inorganic fillers such as charcoal and clay, pigments, diluents, flame retardants, and fungicides.
本発明のビニル壁材の樹脂組成物告発泡体は上記の原料
を配合したペースト状物に、気体あるいは蒸気を吹込む
とか、攪拌すること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や、あらかじ
め上記原料に加熱によって分解し、気体を発生する発泡
剤を添加混合して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、更に高温で加熱発泡させる方法
など、一般に塩化ビニル樹脂発泡体を製造する方法であ
れば、どのような力分布も均一であり、強度の強い、仕
上り外観の良い発泡体が得られるので、本発明のビニル
壁材の樹脂組成物発泡体を得る方法として好ましい。使
用される発泡剤としてはアプリカルボンアミド、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ッド、4.4
’−オキシビスベンセンスルホニルヒドラジノド等の有
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
等無機発泡剤などがあげられる。この発泡剤の添加量は
、塩ヒ樹脂100部に対して1部から30部の範囲であ
る。。The resin composition foam of the vinyl wall material of the present invention is produced by heating the paste while mechanically creating air bubbles by blowing gas or steam into the paste containing the above-mentioned raw materials or by stirring. A method of adding and mixing a foaming agent that decomposes by heating and generating gas to the above raw materials and foaming at the same time as heating and gelling, or a method of further heating and foaming at a high temperature after heating and gelling. In general, any method for producing vinyl chloride resin foam can produce a foam with uniform force distribution, strong strength, and good finished appearance. This is preferred as a method for obtaining a foam. The blowing agents used are apricarbonamide, azobisisobutyronitrile, dinitrosopentamethylenetetramine, paratoluenesulfonyl hydrazide, 4.4
Examples include organic blowing agents such as '-oxybisbenzenesulfonylhydrazinode, and inorganic blowing agents such as sodium bicarbonate, ammonium carbonate, ammonium bicarbonate, azide compounds, and sodium borohydride. The amount of the blowing agent added is in the range of 1 part to 30 parts per 100 parts of the arsenic resin. .
板などを使用することが出来る。ま1こ初詣組成物発泡
体と基体との間に設けられる水不透過層としては非発泡
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、1“:VA4工l(脂、酢酸ビニル樹脂、ポリ
アミド樹脂など、笑質上水を透過せず塩化ビニル樹脂と
接%’j性の良いものであれば、いかなるものでもJ走
いが、塩化ビニル樹脂発泡体との接着性が特に良く、成
型加工性も容易である非発泡の塩化ビニル樹脂にまる層
を設けるのが好ましい。You can use boards etc. The water-impermeable layer provided between the foamed New Year's visit composition and the substrate includes non-foamed vinyl chloride resin, thermoplastic polyurethane resin, acrylic resin, 1":VA4kl (fat, vinyl acetate resin, Any material such as polyamide resin that does not permeate clean water and has good adhesion to vinyl chloride resin can be used, but it has particularly good adhesion to vinyl chloride resin foam, making it suitable for molding. It is preferable to provide a layer made of non-foamed vinyl chloride resin, which is easy to process.
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、カレンター加工法、押出加工法のい
ずれの方法で得られたものでもよい。また該発泡体と基
体との間に水不透過層を設ける方法も、水不透過層を被
覆した基体上に塩化ビニル樹脂発泡体を形成せしめる方
法、水不透過層を被膜した基体の水不過加面と塩化ビニ
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7体化と同時
に接着m1に水不透過層を生成せしめる方法など、適当
な方法で行われる。本発明のビニル壁材を製造する方法
の実施態様の一例としてペースト加工法による場合につ
いて述へれば、発泡剤を含まない非発泡性塩化ビニルプ
ラスチゾルを紺、織布、編布、不繊布などの基体上にド
クターナイフ法、ロールコータニ法などにより出来るた
ケ薄く、一定の厚味で塗布した後、120℃〜170
℃で1部秒から5分間加熱してフラスチソルをゲル化さ
せる。その後その非発泡の塩化ビニル樹脂層を被覆した
基体上に更に高吸水性高力子、発泡剤及びその他補助剤
を含有する塩化ビニルブラスチゾルを上記と同様な方法
で塗布し180℃〜250℃で30秒から5分間加熱発
泡することにより、非発泡の塩化ビニル樹脂層を基体と
発泡層の間に有する本発明の結露防止用ビニル壁材が得
られる。The vinyl chloride resin foam constituting the vinyl wall material of the present invention may be obtained by any of the paste processing method, calendar processing method, and extrusion processing method. There are also methods for providing a water-impermeable layer between the foam and the substrate, such as forming a vinyl chloride resin foam on a substrate coated with a water-impermeable layer, and forming a water-impermeable layer on a substrate coated with a water-impermeable layer. A method for integrating a surface and a vinyl chloride resin foam, a method for integrating a water-impermeable surface of a vinyl chloride resin foam having a water-impermeable layer with a substrate, and a method for integrating a vinyl chloride resin foam and a substrate into a seven-piece structure. At the same time, a suitable method such as a method of forming a water-impermeable layer on the adhesive m1 is carried out. As an example of the embodiment of the method for producing vinyl wall materials of the present invention, when a paste processing method is used, non-foaming vinyl chloride plastisol containing no foaming agent is used to fabricate navy blue, woven fabric, knitted fabric, non-woven fabric, etc. After applying a thin film of a certain thickness to the substrate using the doctor knife method, roll coating method, etc.,
Heat for 1 part second to 5 minutes at 0.degree. C. to gel the frustisol. Thereafter, on the substrate coated with the non-foamed vinyl chloride resin layer, vinyl chloride blastisol containing a highly water-absorbent high strength element, a foaming agent, and other auxiliary agents was further applied in the same manner as above, and heated at 180°C to 250°C. By heating and foaming for 30 seconds to 5 minutes, the vinyl wall material for preventing dew condensation of the present invention having a non-foamed vinyl chloride resin layer between the base and the foam layer can be obtained.
本発明の壁材を使用して室FF3壁面、押入れの壁など
の結露を防止する場合、壁材を適切な厚さにすべきであ
る。容易に理j!l’f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埋さによっても異なるから
である。壁材として必要な厚さは0.1〜B態であり中
でも03訴〜1.5黙が適当である。When using the wall material of the present invention to prevent condensation on the wall of room FF3, the wall of the closet, etc., the wall material should have an appropriate thickness. Easy to understand! This is because, as described above, the dew condensation prevention effect of wall materials, that is, their water retention capacity, differs depending on how buried they are. The required thickness for the wall material is 0.1 to B, and 03 to 1.5 is suitable.
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。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1こりすることはもちろA7、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
ことはすべてとり入れることが出来る。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した方が艮い。The vinyl wall material of the present invention is capable of many modifications, both in construction and manufacturing method. For normal wall material products, such as applying appropriate surface treatment, patterning, and embossing on the surface of A7, and applying adhesive to the back and applying release paper. Everything that is done can be taken in. Embossing is especially effective because it increases the surface area and creates a shape that absorbs moisture easily.
また、表面処理や柄付けをする場合、処理剤を全面に塗
布すると被膜が出来で吸水性の悪くなる場合があるので
、メツシュロール等を使用して処理を行う方が好ましい
。In addition, when performing surface treatment or patterning, it is preferable to use a mesh roll or the like to perform the treatment, since applying a treatment agent to the entire surface may form a film and reduce water absorption.
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t、 y: 水分は
、壁材を構成してい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く完全に水分の結露
が防止される。さらに本発明の結露防止用ビニル壁材は
この塩化ビニル樹脂発泡層に吸水され1こ水分が裏打の
基体に移行しないので、水分による基体の伸びや、カビ
の発生や、腐敗による糊材の劣化が防止され、その結果
長期間にわ1こってきれいに貼っfコ状態が維持される
。ま1こ本発明のビニル壁材は高湿度下では急速に水分
を吸収し、また低湿度下では水分を放出する、いわゆる
呼+1i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出来る。By using the vinyl wall material for preventing condensation of the present invention,
Even during humid times such as the rainy season, condensation t, y: Moisture is absorbed by the vinyl chloride resin foam layer that makes up the wall material, and no water droplets appear on the surface, completely preventing condensation. Ru. Furthermore, in the vinyl wall material for preventing dew condensation of the present invention, water is absorbed by the polyvinyl chloride resin foam layer and the moisture does not transfer to the backing substrate, which prevents stretching of the substrate due to moisture, growth of mold, and deterioration of the glue material due to rot. As a result, the adhesive remains neatly stuck for a long period of time. First, the vinyl wall material of the present invention rapidly absorbs moisture under high humidity and releases moisture under low humidity, which is the so-called +1i property, so it can be used for the purpose of humidity control in small rooms etc. You can also do it.
以上詳述したように、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、天井の壁装材として使用されるばかりでなく、コ
ンテナー等の内壁の結露防止用壁材としても利用出来る
。以下に実施例を挙げて本発明の結露防止用壁材を更に
説明するが、本発明はこれらに限定されろものではない
。As detailed above, the vinyl wall material for preventing condensation of the present invention is not only used as a wall covering material for walls and ceilings of living rooms, kitchens, toilets, bathrooms, washrooms, closets, etc., but also for containers, etc. It can also be used as a wall material to prevent condensation on the inner walls of buildings. The wall material for preventing dew condensation of the present invention will be further explained below with reference to Examples, but the present invention is not limited thereto.
実施例1〜2
酢酸ビニル60fとアクリル酸メチル40デに重合開始
剤として、ラウロイルパーオキシドo、tyを加え、部
分ケン化ポリヒニルアルコ−JvB9−とNaC1!1
0 Fを含む水300・l中に攪拌分散せしめ65℃で
6時間懸濁重合した。この共重合体86y−を2001
のメタノールと水lozおよび5NのNaOH水溶液4
0−からなるケン化液中に懸濁し、25℃で1時局、次
いで65℃で5時間ケン化反応を行った。メタノールで
十分洗浄した後、減圧乾燥して平均粒径200μのケン
化物(吸水倍率700 Vfl−の吸水能力を有する)
を得た。これをジェッ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9゜゛ この高吸水性高分
子と塩化ビニル樹脂を用いて第1表に示す配合物をテス
パーにより混合攪拌し、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整しtこ。Examples 1 to 2 Lauroyl peroxide o, ty was added as a polymerization initiator to vinyl acetate 60f and methyl acrylate 40, and partially saponified polyhinyl alcohol-JvB9- and NaC1!1 were prepared.
The mixture was stirred and dispersed in 300 liters of water containing 0 F, and suspension polymerized at 65°C for 6 hours. This copolymer 86y-2001
methanol and water loz and 5N NaOH aqueous solution 4
The suspension was suspended in a saponification solution consisting of 0- and saponification reaction was carried out at 25°C for 1 hour and then at 65°C for 5 hours. After thorough washing with methanol, dry under reduced pressure to obtain a saponified product with an average particle size of 200μ (water absorption capacity of 700 Vfl-)
I got it. This was pulverized by a jet mill to obtain a finely powdered superabsorbent polymer with a particle size of 60μ or less.9゛ Using this superabsorbent polymer and vinyl chloride resin, the formulations shown in Table 1 were mixed and stirred using a Tesper. A uniform paste-like vinyl chloride plastisol composition for the foam layer was prepared.
第 1 表
一方、上記配合物よりあらかじめアゾシカ−ボンアミド
と高吸水性樹脂を除いtこ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整した。次に紙
材上に上記、非発泡性塩化ビニルブラスチゾルをo、
t m厚でナイフコーティングして、続いて150℃、
30秒加熱してゲル化せしめ1こ。更にその上に上記発
泡層用塩化ビニルプラスチゾルを0.2語厚で同様にコ
ーティングし、220℃、1分で加熱発泡させ、エンホ
スロールによって゛エンボス加工を施し、ビニル壁材を
得1こっ比較例1
紙上にあらかじめ非発泡性塩化ビニル層をコーティング
せずに、実施例2の配合による発泡層を実施例と同様の
方法で複機せしめ1こ従来技術によるビニル壁材を得た
。Table 1 On the other hand, the azocicabonamide and the superabsorbent resin were removed from the above formulation and the mixture was made into a paste in the same manner to prepare a non-foamable vinyl chloride plastisol. Next, apply the above non-foaming vinyl chloride blastisol on the paper material.
Knife coating at t m thickness followed by 150°C;
Heat 1 cup for 30 seconds to gel. Furthermore, the above-mentioned vinyl chloride plastisol for the foam layer was coated in the same manner at a thickness of 0.2 layers, heated and foamed at 220°C for 1 minute, and embossed with an embossing roll to obtain a vinyl wall material. Example 1 A foamed layer having the formulation of Example 2 was compounded in the same manner as in Example without coating the paper with a non-foamed vinyl chloride layer in advance to obtain a vinyl wall material according to the prior art.
比較例2
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
配合物を実施例と同様にペースト化し、紙上にコーティ
ングし、加熱発泡せしめてビニル壁材を得た。Comparative Example 2 The composition of Example 2 except that the superabsorbent polymer was removed in advance was made into a paste in the same manner as in the example, coated on paper, and heated and foamed to obtain a vinyl wall material.
比較例3
実施例2の配合よりあらかじめアゾシカ−ボンアミドを
除いた配合物を実施例と同様にペースト化し、紙の上に
コーティングして加熱ケル化せしめてビニル壁材を得た
。Comparative Example 3 The formulation of Example 2 except that azosicabonamide was removed in advance was made into a paste in the same manner as in the example, and the paste was coated on paper and heated to melt to obtain a vinyl wall material.
実用試験l
上記実施例1.2、比較例1.2.3のビニル壁材を室
内温度35℃、相対湿1190%、壁材裏面温度IO℃
の条件で結露性試験を行った結果を表2に示す。Practical test l The vinyl wall materials of Example 1.2 and Comparative Example 1.2.3 were tested at an indoor temperature of 35°C, a relative humidity of 1190%, and a temperature on the back surface of the wall material of IO°C.
Table 2 shows the results of a dew condensation test conducted under these conditions.
実施例1.2の壁材は結露がなく、24時間後も完〈変
化がなかったが、比較例1の壁側は表面の感触は実施例
1.2と同様であっtこが一部に壁利のtこるみが生じ
ていた。比較例2.3の壁材は結露を生じ、壁面を水が
滴下していた。The wall material of Example 1.2 had no condensation and remained completely unchanged even after 24 hours, but the wall material of Comparative Example 1 had the same surface feel as Example 1.2. There was a stiffness in the wall. The wall materials of Comparative Examples 2 and 3 had condensation, and water was dripping down the wall surface.
実用試験2
上記実施例1.2、比較例1.2のビニル壁材を夜間結
露する壁面に通常の澱粉糊を使用して貼りつけ、その効
果および長期間の変形などを調べ表3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
にあったが夜になると差が認められ、実施例112、比
較例1の壁材はサラッとした感触を保っていたが、比較
例2の壁材は結露を生じて表面が湿っていtコ。再び温
度が高(湿度の低い条件になると各サンプルとも乾燥状
態となった。60日間の継続観察の終りには、実施例1
,2の壁材は貼付けたままの状態で変化がなかったが、
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の従来技術による壁材にはた
るみが生じ、表面はかびやしみなどにより汚れていた。Practical Test 2 The vinyl wall materials of Example 1.2 and Comparative Example 1.2 above were pasted on a wall surface where dew condenses at night using normal starch glue, and the effects and long-term deformation were investigated and shown in Table 3. Ta. When the daytime temperature was high, all four samples were in a dry state, but at night there was a difference, and the wall materials of Example 112 and Comparative Example 1 maintained a smooth feel, but The wall material of Comparative Example 2 had a damp surface due to condensation. When the temperature became high (low humidity) again, each sample became dry. At the end of 60 days of continuous observation, Example 1
,2 The wall material remained attached and remained unchanged.
The wall material of Comparative Example 1 had peeled from the wall surface, and mold had grown in the peeled part. The conventional wall material of Comparative Example 2 sagged, and the surface was stained with mold and stains.
比較例1の壁材を疎水性、耐水性を有する接着剤を使用
して貼付けた場合は、壁材と壁面との剥離は生じていな
かったが、壁材のたるみによる、しわが生じてい1こ。When the wall material of Comparative Example 1 was attached using a hydrophobic and water-resistant adhesive, there was no peeling between the wall material and the wall surface, but wrinkles did occur due to sagging of the wall material. child.
表 3 11 0 はとんどなし Δ 部分的にあり × 全体にありTable 3 11 0 is almost impossible Δ Partially present × Available throughout
Claims (4)
塑剤からなる樹脂組成物発泡体と、それを被覆した基体
よりなる結露防止用ビニル壁材において、発泡層と基体
との間に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。(1) Chloride 5゛°ruti! In a vinyl wall material for preventing dew condensation consisting of a resin composition foam made of H5 super absorbent polymer 3 and a plasticizer and a base coated with it, a water-impermeable layer is provided between the foam layer and the base. Vinyl wall material for preventing condensation.
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。(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.
レン系不飽和カルボン酸またはその誘導体(Y ) y
t主成分トL、T、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iF齢の鋏註防ル用賠材−(3) The super absorbent polymer is vinyl ester (X) and ethylenically unsaturated carboxylic acid or its derivative (Y) y
Claim 1: A saponified copolymer consisting of main components L, T, and X:Y in a molar ratio of 10:90 to 90:10. Materials for use
樹脂である特許請求の範囲第1項、第2項又は第3項記
載の結露防止用ビニル壁材。(4) The vinyl wall material for preventing dew condensation according to claim 1, 2, or 3, wherein the water-impermeable layer is made of non-foamed vinyl chloride resin or amide resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58189023A JPS6081378A (en) | 1983-10-07 | 1983-10-07 | Vinyl wall material for preventing condensation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58189023A JPS6081378A (en) | 1983-10-07 | 1983-10-07 | Vinyl wall material for preventing condensation |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6081378A true JPS6081378A (en) | 1985-05-09 |
JPH0524273B2 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 | Vinyl wall material for preventing condensation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6081378A (en) |
Cited By (4)
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)
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 |
-
1983
- 1983-10-07 JP JP58189023A patent/JPS6081378A/en active Granted
Patent Citations (4)
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 |
Cited By (5)
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 |
JPH0542952B2 (en) * | 1989-04-20 | 1993-06-30 | Toyo Tire & Rubber Co | |
JPH0494438U (en) * | 1990-12-26 | 1992-08-17 |
Also Published As
Publication number | Publication date |
---|---|
JPH0524273B2 (en) | 1993-04-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3714078A (en) | Foamable acrylic latex composition and method of preparation | |
JP3625069B2 (en) | Decorative sheet and manufacturing method thereof | |
JP2001504539A (en) | Foam coating method | |
JP4139155B2 (en) | Breathable wallpaper and method for producing the same | |
JP2002096433A (en) | Wall paper | |
JPS6081378A (en) | Vinyl wall material for preventing condensation | |
US3034944A (en) | Water-activated prepasted plastic sheeting | |
JPH0255742A (en) | Preparation of foamed polyvinyl alcohol film | |
KR102436617B1 (en) | Eco-friendly foaming wallpaper and method for preparing the same | |
JP2002155478A (en) | Highly foamed wall paper | |
KR100341277B1 (en) | Functional fabrics containing cork and a method preparing the same | |
KR102436619B1 (en) | Eco-friendly foaming wallpaper and method for preparing the same | |
JP3401916B2 (en) | How to make wallpaper | |
JP3667269B2 (en) | Aqueous emulsion resin composition and foamed wallpaper using the same | |
JP2890203B2 (en) | Manufacturing method of foam decorative material | |
JPS62231740A (en) | Hygroscopic and damp-discharging vinyl wall material and manufacture thereof | |
GB2135903A (en) | Adhesive foams | |
JPH04337345A (en) | Gloss-controlling resin composition | |
JP4059561B2 (en) | Laminated body | |
JP2004042520A (en) | Plasticizer-resistant multilayered foamed decorative material | |
JPS6018315B2 (en) | Decorative materials and manufacturing methods thereof | |
JPH01260098A (en) | Wall paper and production thereof | |
JPH09157427A (en) | Paste-like composition and laminate having synthetic resin layer prepared by using the same | |
JPH02274528A (en) | Manufacture of sheet form article | |
JP4476383B2 (en) | Cosmetic material having moisture absorption / release performance and method for producing the same |