JPH0667575B2 - Interior material manufacturing method - Google Patents
Interior material manufacturing methodInfo
- Publication number
- JPH0667575B2 JPH0667575B2 JP2085946A JP8594690A JPH0667575B2 JP H0667575 B2 JPH0667575 B2 JP H0667575B2 JP 2085946 A JP2085946 A JP 2085946A JP 8594690 A JP8594690 A JP 8594690A JP H0667575 B2 JPH0667575 B2 JP H0667575B2
- Authority
- JP
- Japan
- Prior art keywords
- porous body
- impregnated
- polyvalent isocyanate
- interior material
- block
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000463 material Substances 0.000 title claims description 13
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000012948 isocyanate Substances 0.000 claims description 31
- -1 isocyanate compound Chemical class 0.000 claims description 25
- 238000000465 moulding Methods 0.000 claims description 15
- 230000003014 reinforcing effect Effects 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 7
- 230000008929 regeneration Effects 0.000 claims description 5
- 238000011069 regeneration method Methods 0.000 claims description 5
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 150000002513 isocyanates Chemical class 0.000 description 8
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 7
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920003002 synthetic resin Polymers 0.000 description 6
- 239000000057 synthetic resin Substances 0.000 description 6
- 238000007598 dipping method Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 229920005830 Polyurethane Foam Polymers 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 239000002981 blocking agent Substances 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 4
- 239000004745 nonwoven fabric Substances 0.000 description 4
- 239000011496 polyurethane foam Substances 0.000 description 4
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- IYXGSMUGOJNHAZ-UHFFFAOYSA-N Ethyl malonate Chemical compound CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 description 3
- 239000004640 Melamine resin Substances 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 239000001119 stannous chloride Substances 0.000 description 3
- 235000011150 stannous chloride Nutrition 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- WDJHALXBUFZDSR-UHFFFAOYSA-N Acetoacetic acid Natural products CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 230000002787 reinforcement Effects 0.000 description 2
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- NQEZDDPEJMKMOS-UHFFFAOYSA-N 4-trimethylsilylbut-3-yn-2-one Chemical compound CC(=O)C#C[Si](C)(C)C NQEZDDPEJMKMOS-UHFFFAOYSA-N 0.000 description 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- TUEIURIZJQRMQE-UHFFFAOYSA-N [2-(tert-butylsulfamoyl)phenyl]boronic acid Chemical compound CC(C)(C)NS(=O)(=O)C1=CC=CC=C1B(O)O TUEIURIZJQRMQE-UHFFFAOYSA-N 0.000 description 1
- 229920006221 acetate fiber Polymers 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- YMLFYGFCXGNERH-UHFFFAOYSA-K butyltin trichloride Chemical compound CCCC[Sn](Cl)(Cl)Cl YMLFYGFCXGNERH-UHFFFAOYSA-K 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- PKKGKUDPKRTKLJ-UHFFFAOYSA-L dichloro(dimethyl)stannane Chemical compound C[Sn](C)(Cl)Cl PKKGKUDPKRTKLJ-UHFFFAOYSA-L 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- PWEVMPIIOJUPRI-UHFFFAOYSA-N dimethyltin Chemical compound C[Sn]C PWEVMPIIOJUPRI-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- JEGUKCSWCFPDGT-UHFFFAOYSA-N h2o hydrate Chemical compound O.O JEGUKCSWCFPDGT-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
- 229940080818 propionamide Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Vehicle Interior And Exterior Ornaments, Soundproofing, And Insulation (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は主として自動車の天井材、扉トリム、リアパー
セル等の内装材の製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial field of application] The present invention mainly relates to a method for manufacturing an interior material such as a ceiling material, a door trim and a rear parcel of an automobile.
従来、この種の内装材の製造方法としては、多価イソシ
アナート化合物を多孔質体に含浸させ、水蒸気あるいは
水を噴霧することによって多価イソシアナートを高分子
化かつ網状化せしめるとともに該多孔質体を所定形状に
成形する方法が提供されている(例えば特開昭58−5346
号)。Conventionally, as a method for producing an interior material of this type, a polyvalent isocyanate compound is impregnated in a porous body, and the polyvalent isocyanate is polymerized and reticulated by spraying steam or water to the porous body. A method for forming a body into a predetermined shape is provided (for example, Japanese Patent Laid-Open No. 58-5346).
issue).
しかしながら、上記従来の方法においては多価イソシア
ナート化合物を含浸した多孔質体に水蒸気あるいは水を
噴霧した時点から該多価イソシアナート化合物の硬化反
応が開始されるので、該多価イソシアナート化合物に水
分が接触してから成形するまでの時間によって該多価イ
ソシアナート化合物の硬化に大きなばらつきが生じ、品
質が一定しないと云う問題点があった。However, in the above-mentioned conventional method, the curing reaction of the polyvalent isocyanate compound is started from the point of time when water vapor or water is sprayed on the porous body impregnated with the polyvalent isocyanate compound. There has been a problem that the quality of the polyvalent isocyanate compound varies greatly depending on the time from the contact with water until the molding, and the quality is not constant.
本発明は上記従来の課題を解決するための手段として、
160℃以下の温度で再生するブロック多価イソシアナー
ト化合物を多孔質体に含浸させ、該ブロック多価イソシ
アナート化合物の再生温度以上の温度で該多孔質体を所
定形状に成形する内装材の製造方法を提供するものであ
る。The present invention, as a means for solving the above conventional problems,
Production of an interior material in which a block polyvalent isocyanate compound that regenerates at a temperature of 160 ° C. or less is impregnated into a porous body, and the porous body is molded into a predetermined shape at a temperature equal to or higher than the regeneration temperature of the block polyvalent isocyanate compound It provides a method.
本発明に用いられる多孔質体としては軟質ポリウレタン
発泡体シート、軟質ポリ塩化ビニル発泡体シートのよう
な軟質なプラスチックの連続気泡を有する発泡体シー
ト、不織布、フェルトのような繊維絡合体シート等が例
示される。Examples of the porous material used in the present invention include a soft polyurethane foam sheet, a foam sheet having open cells of a soft plastic such as a soft polyvinyl chloride foam sheet, a non-woven fabric, and a fiber entangled sheet such as felt. It is illustrated.
本発明に用いられる多価イソシアナート化合物としては
2,4または2,6−トルエンジイソシアナート、ヘキサメチ
レンジイソシアナート、4,4′−ジフェニルメタンジイ
ソシアナート等の多価イソシアナート単量体、あるいは
該単量体のエチレングリコール、グリセリン等の多価ア
ルコールとのアダクト、あるいは該単量体とポリエチレ
ングリコール、ポリプロピレングリコール等のポリアル
キレングリコールと反応させ末端に遊離イソシアナート
基を二個以上有するプレポリマー等が例示される。上記
多価イソシアナート化合物をブロックする。ブロック剤
としてはマロン酸ジエチルエステル、アセト酢酸エステ
ル、アセチルアセトン、青酸、酸性亜硫酸ナトリウム等
があり、このようなブロック剤でブロックした多価イソ
シアナート化合物は160℃以下の温度の加熱によって再
生する。多価イソシアナート化合物の再生温度はブロッ
ク剤がマロン酸ジエチルエステルの場合は130〜140℃、
アセト酢酸エステルの場合は140℃、アセチルアセトン
の場合は150℃、青酸の場合は120℃、酸性亜硫酸ナトリ
ウムの場合は40〜50℃である。As the polyvalent isocyanate compound used in the present invention,
2,4 or 2,6-toluene diisocyanate, hexamethylene diisocyanate, polyvalent isocyanate monomer such as 4,4′-diphenylmethane diisocyanate, or ethylene glycol or glycerin of the monomer Examples thereof include adducts with polyhydric alcohols, or prepolymers having two or more free isocyanate groups at the ends obtained by reacting the monomers with polyalkylene glycols such as polyethylene glycol and polypropylene glycol. Block the polyisocyanate compound. Examples of the blocking agent include malonic acid diethyl ester, acetoacetic acid ester, acetylacetone, hydrocyanic acid, and sodium acid sulfite. The polyvalent isocyanate compound blocked with such a blocking agent is regenerated by heating at a temperature of 160 ° C. or lower. The regeneration temperature of the polyvalent isocyanate compound is 130 to 140 ° C when the blocking agent is malonic acid diethyl ester,
In the case of acetoacetic acid ester, the temperature is 140 ° C, in the case of acetylacetone, 150 ° C, in the case of hydrocyanic acid, 120 ° C, and in the case of sodium acid sulfite, the temperature is 40 to 50 ° C.
上記各例示は本発明を限定するものではない。The above examples do not limit the present invention.
上記ブロック多価イソシアナート化合物を多孔質体に含
浸させるためには、上記ブロック多価イソシアナート化
合物が液状のものであればそのまゝ、あるいはトルエ
ン、キシレン、酢酸エチル、酢酸n−ブチル、アセト
ン、メチルエチルケトン、メチレンジクロライド、トリ
クロロエチレン等の有機溶剤に溶解して溶液にするか、
あるいは上記ブロック多価イソシアナート化合物を界面
活性剤を用いて水に乳化させてエマルジョンにする。In order to impregnate the porous material with the block polyvalent isocyanate compound, the block polyvalent isocyanate compound may be in the form of a liquid, or toluene, xylene, ethyl acetate, n-butyl acetate, or acetone. , Dissolved in an organic solvent such as methyl ethyl ketone, methylene dichloride, trichlorethylene, etc.
Alternatively, the block polyvalent isocyanate compound is emulsified in water using a surfactant to form an emulsion.
上記ブロック多価イソシアナート化合物の溶液またはエ
マルジョンには所望なれば水および/また水酸基、カル
ボキシ基、アミノ基等の活性水素を有しイソシアナート
と反応可能な官能基を有する化合物および/または合成
樹脂が混合されてもよい。上記化合物としてはメタノー
ル、エタノール、イソプロパノール、n−ブタノール、
エチレングリコール、プロピレングリコール、グリセリ
ン等のアルコール類、蟻酸、酢酸、酪酸、蓚酸、クエン
酸、マロン酸等の有機酸、トリエチルアミン、トリエタ
ノールアミン、ジイソプロピルアミン、アセトアミド、
プロピオン酸アミド等の有機アミン類または酸アミド等
があり、上記合成樹脂としては上記官能基を有するアク
リル樹脂、スチレン樹脂、酢酸ビニル樹脂、尿素樹脂、
メラミン樹脂、フェノール樹脂、エポキシ樹脂等があ
る。If desired, the solution or emulsion of the block polyvalent isocyanate compound may be water and / or a compound and / or a synthetic resin having a functional group having an active hydrogen such as a hydroxyl group, a carboxy group or an amino group and capable of reacting with an isocyanate. May be mixed. Examples of the above compound include methanol, ethanol, isopropanol, n-butanol,
Alcohols such as ethylene glycol, propylene glycol, glycerin, organic acids such as formic acid, acetic acid, butyric acid, oxalic acid, citric acid, malonic acid, triethylamine, triethanolamine, diisopropylamine, acetamide,
There are organic amines such as propionamide and acid amides, and the synthetic resin is an acrylic resin having the above functional group, a styrene resin, a vinyl acetate resin, a urea resin,
There are melamine resin, phenol resin, epoxy resin and the like.
更に上記多価イソシアナート化合物にはナフテン酸コバ
ルト、ベンジルトリメチルアンモニウムハイドロオキサ
イド、塩化第一スズ、トリ−n−ブチルチンアセテー
ト、n−ブチルチントリクロライド、トリメチルチンハ
イドロオキサイド、ジメチルチンジクロライド、ジメチ
ルチンジラウレート等の触媒が添加されてもよい。Further, the polyvalent isocyanate compound includes cobalt naphthenate, benzyltrimethylammonium hydroxide, stannous chloride, tri-n-butyltin acetate, n-butyltin trichloride, trimethyltin hydroxide, dimethyltin dichloride, dimethyltin. A catalyst such as dilaurate may be added.
該溶液もしくはエマルジョンを上記多孔質体にスプレー
したり、該溶液中に上記多孔質体を浸積したりする。上
記ブロック多価イソシアナート化合物を上記多孔質体に
含浸した後所望なればロール絞り等で含浸量を調節した
後常温または加熱乾燥を行なう。上記ブロック多価イソ
シアナート化合物を通常上記多孔質体に50〜150重量%
程度含浸される。The solution or emulsion is sprayed on the porous body, or the porous body is immersed in the solution. After impregnating the above-mentioned block polyvalent isocyanate compound into the above-mentioned porous body, if desired, the impregnation amount is adjusted with a roll squeeze or the like, and then it is carried out at room temperature or heated and dried. The above block polyvalent isocyanate compound is usually added to the above porous body in an amount of 50 to 150% by weight.
Impregnated to a degree.
上記ブロック多価イソシアナート化合物を含浸した上記
多孔質体はそれからプレス成形等によって所定の形状に
加熱成形する。該プレス成形は上記ブロック多価イソシ
アナート化合物の再生温度以上の温度、通常130〜160℃
程度の温度で行なわれる。The porous body impregnated with the block polyvalent isocyanate compound is then heat-molded into a predetermined shape by press molding or the like. The press molding is performed at a temperature above the regeneration temperature of the block polyvalent isocyanate compound, usually 130 to 160 ° C.
It is carried out at a moderate temperature.
上記成形に先立って上記ブロック多価イソシアナート化
合物を含浸した多孔質体に水および/またはイソシアナ
ートと反応可能な官能基を有する化合物および/または
合成樹脂、あるいは上記水、官能基含有化合物、合成樹
脂に上記触媒を添加した溶液またはエマルジョンが噴霧
あるいは浸漬等の手段で付加されてもよい。A compound and / or a synthetic resin having a functional group capable of reacting with water and / or an isocyanate in a porous material impregnated with the block polyvalent isocyanate compound prior to the molding, or the water, a compound containing a functional group, and synthesis. A solution or emulsion in which the above catalyst is added to the resin may be added by means such as spraying or dipping.
上記のようにして本発明の方法によって内装材が成形さ
れるが、本発明においては上記多孔質体に所定の着色を
施してもよい。また成形前、成形時、あるいは成形後に
上記多孔質体の両面または片面に合成樹脂含浸紙や多孔
補強層を重合してもよい。該合成樹脂含浸紙とはアクリ
ル樹脂、スチレン樹脂、酢酸ビニル樹脂、塩化ビニル樹
脂、エポキシ樹脂、ウレタン樹脂、尿素樹脂、メラミン
樹脂、フェノール樹脂等を含浸せしめた紙のことであ
り、該多孔補強層とは目付60〜200g/m2程度の粗目の不
織布または編織物、金属、ガラス繊維紐、有機繊維紐、
紙紐等で編成したネット、紙、不織布、金属導板等にパ
ンチングを施した多孔層等である。上記各例示は本発明
を限定するものではない。該合成樹脂含浸紙あるいは該
多孔補強層を上記多孔質体に重合した上に更にポリステ
ル繊維、アクリル繊維、アセテート繊維等の合成繊維の
編層に合成樹脂含浸紙に使用されている合成樹脂と同様
な合成樹脂を含浸させた合成樹脂含浸編層を重合しても
よい。Although the interior material is molded by the method of the present invention as described above, in the present invention, the porous body may be colored in a predetermined manner. Further, before or during molding, or after molding, synthetic resin-impregnated paper or a porous reinforcing layer may be polymerized on both surfaces or one surface of the porous body. The synthetic resin-impregnated paper is paper impregnated with acrylic resin, styrene resin, vinyl acetate resin, vinyl chloride resin, epoxy resin, urethane resin, urea resin, melamine resin, phenol resin, etc., and the porous reinforcing layer Is a coarse non-woven or knitted fabric with a basis weight of about 60 to 200 g / m 2 , metal, glass fiber string, organic fiber string,
Examples include a net knitted with a paper string or the like, paper, a non-woven fabric, a porous layer obtained by punching a metal conducting plate, or the like. The above examples do not limit the present invention. The synthetic resin-impregnated paper or the porous reinforcing layer is polymerized into the above-mentioned porous body, and further, a knitting layer of synthetic fibers such as polyester fiber, acrylic fiber, acetate fiber, etc. is the same as the synthetic resin used for the synthetic resin-impregnated paper. A synthetic resin-impregnated knit layer impregnated with another synthetic resin may be polymerized.
上記合成樹脂含浸紙や上記多孔補強層は接着剤や感熱性
接着シートによって上記多孔質体に接着せられるが、こ
のような接着剤を用いることなく、上記多孔質体に含浸
せられているブロック多価イソシアナートを接着剤とし
て用いることも可能である。また上記合成樹脂含浸編層
も接着剤を用いるかまたは該編層に含浸せられている合
成樹脂を接着剤として上記合成樹脂含浸紙や上記多孔補
強層に接着することが出来、特に上記多孔補強層の場合
には該編層は該多孔補強層の多孔を介して直接上記多孔
質体に接着することが出来る。The synthetic resin-impregnated paper and the porous reinforcing layer are adhered to the porous body by an adhesive or a heat-sensitive adhesive sheet, but the block impregnated in the porous body without using such an adhesive. It is also possible to use polyvalent isocyanate as an adhesive. Further, the synthetic resin-impregnated knitted layer can also be bonded to the synthetic resin-impregnated paper or the porous reinforcing layer using an adhesive agent or the synthetic resin impregnated in the knitted layer can be used as an adhesive agent, and in particular, the porous reinforcing layer can be used. In the case of a layer, the knitted layer can be directly bonded to the porous body through the porosity of the porous reinforcing layer.
ブロック多価イソシアナート含浸多孔質体を再生温度以
上の温度で加熱成形すると、前記したようにイソシアナ
ート基とブロック剤との結合が加熱によって解離して遊
離のイソシアナート基が再生、多価イソシアナート化合
物は該イソシアナート基を介して高分子化かつ網状化す
ることにより該多価イソシアナートが硬化し該多孔質体
を所定の成形形状に保持する。When the block polyvalent isocyanate impregnated porous body is heat-molded at a temperature equal to or higher than the regeneration temperature, the bond between the isocyanate group and the blocking agent is dissociated by heating to regenerate the free isocyanate group as described above, and the polyvalent isocyanate is regenerated. When the nato compound is polymerized and networked through the isocyanate group, the polyvalent isocyanate is cured and the porous body is maintained in a predetermined molded shape.
したがって本発明において成形にブロック多価イソシア
ナート化合物のイソシアナート基が再生し硬化するか
ら、該多価イソシアナート化合物の硬化状態のばらつき
は解消され、均一な品質の製品を得ることが出来る。Therefore, in the present invention, since the isocyanate group of the block polyvalent isocyanate compound is regenerated and cured during molding, variations in the curing state of the polyvalent isocyanate compound are eliminated, and a product of uniform quality can be obtained.
また本発明において、多孔質体に着色を施しておけばそ
れ自体が表装性を有することになり、表装材を貼着する
ことが必要なくなる。Further, in the present invention, if the porous body is colored, the porous body itself has a covering property, and it is not necessary to attach a covering material.
更に本発明において合成樹脂含浸紙を多孔質体に重合す
れば、該多孔質体が補強され成形形状安定性や耐熱性が
向上する。Further, when the synthetic resin-impregnated paper is polymerized into a porous body in the present invention, the porous body is reinforced and the molding shape stability and heat resistance are improved.
また更に本発明において多孔補強層を多孔質体に重合し
た場合も同様に多孔質体が補強されるが、多孔補強層の
場合は伸縮性が良好で成形形状に追随性が大であり、深
絞り成形等によっても亀裂等を生じない。Further, in the present invention, when the porous reinforcement layer is polymerized into a porous body, the porous body is similarly reinforced, but in the case of the porous reinforcement layer, the stretchability is good and the conformability to the molded shape is large, No cracks or the like are generated even by drawing.
実施例1 第1図および第2図には本発明に用いられる装置の一実
施例が示される。(1)はポリエーテル型軟質ポリウレ
タン発泡体シート(密度0.017g/cm3、厚み5mm)であ
り、該シート(1)はガイドロール(2)に案内されて
浸積槽(3)に導入され、浸積槽(3)にはマロン酸ジ
エチルエステルによってブロックされた4,4′−ジフェ
ニルメタンジイソシアナート(MDI)の40重量%トリク
ロルエチレン溶液(9)が充填され、該浸積槽(3)に
おいて該シート(1)は該溶液中で圧縮ロール(4),
(5)により2回圧縮されつゝ該ブロックMDI溶液
(9)が含浸せられ、その後浸積槽(3)から出て絞り
ロール(6)により該ブロックされているMDI含浸量を
約100g/m2に調節される。該ブロックMDI含浸シート
(1)Aはその後70℃の通風乾燥機(7)に送られ5分
間乾燥された後カッター(8)によって適当な寸法に裁
断される。Embodiment 1 FIGS. 1 and 2 show an embodiment of the apparatus used in the present invention. (1) is a polyether type soft polyurethane foam sheet (density 0.017 g / cm 3 , thickness 5 mm), and the sheet (1) is guided by a guide roll (2) and introduced into a dipping tank (3). The dipping tank (3) was filled with a 40% by weight trichloroethylene solution (9) of 4,4′-diphenylmethane diisocyanate (MDI) blocked with malonic acid diethyl ester, and the dipping tank (3) The sheet (1) in the solution is compressed rolls (4),
The block MDI solution (9) is impregnated twice with (5) and then the block MDI solution (9) is discharged from the dipping tank (3) and the blocked MDI impregnation amount is about 100 g / Adjusted to m 2 . The block MDI-impregnated sheet (1) A is then sent to a ventilation dryer (7) at 70 ° C., dried for 5 minutes, and then cut into an appropriate size by a cutter (8).
裁断された該ブロックMDI含浸シート(1)Aはその後
第2図に示すように上型(10)Aと下型(10)Bとから
なる加熱押圧成形型(10)において目付70g/m2の粗目
ポリエステル不織布に塩化第一スズを1重量%含むエチ
レン−酢酸ビニル共重合体50重量%エマルジョンを50g
/m2の割合で含浸させた未乾燥の補強槽(1)Bを重合
し、150℃,3kg/cm2の成形条件で所定形状に成形され
る。Shredded the block MDI impregnated sheet (1) A basis weight 70 g / m 2 in the upper mold, as subsequently shown in FIG. 2 (10) A and the lower mold (10) heated press mold composed of a B (10) 50g ethylene-vinyl acetate copolymer 50wt% emulsion containing 1wt% stannous chloride in coarse polyester nonwoven fabric
The undried reinforcing tank (1) B impregnated at a ratio of / m 2 is polymerized and molded into a predetermined shape under molding conditions of 150 ° C. and 3 kg / cm 2 .
上記成形においてシート(1)Aに含浸されている該ブ
ロックMDIは加熱によりイソシアナート基を再生し、上
記エチレン−酢酸ビニル共重合体エマルジョンに含まれ
ている水および塩化第一スズによって急激に硬化する。In the above-mentioned molding, the block MDI impregnated in the sheet (1) A regenerates an isocyanate group by heating, and is rapidly cured by water and stannous chloride contained in the ethylene-vinyl acetate copolymer emulsion. To do.
このようにして成形形状安定性の良好な、そして軽量で
防音性に富む内装材が得られる。In this way, it is possible to obtain an interior material having good molding shape stability, light weight, and excellent soundproofing.
実施例2 実施例1のブロックMDIに代えてアセチルアセトンによ
ってブロックされたトルエンジイソシアナート(TDI)3
0重量%、メチルメタクリレート:ジメチルアミノエチ
ルメタクリレートの3:1共重合体10重量%を含むトリク
ロルエチレン溶液を実施例1で使用した軟質ポリウレタ
ン発泡体シートに実施例1と同様にして含浸させてブロ
ックTDI含浸シートを作成し、該ブロックTDI含浸シート
の両面にメラミン樹脂水溶液(50重量%)を60g/m2の
割合で含浸させたガラス繊維不織布(目付80g/m2)を
重合して160℃、3kg/cm2の成形条件で所定形状に成形
した。Example 2 Toluene diisocyanate (TDI) 3 blocked with acetylacetone instead of the block MDI of Example 1
The soft polyurethane foam sheet used in Example 1 was impregnated with a trichlorethylene solution containing 0% by weight and a 3: 1 copolymer of methylmethacrylate: dimethylaminoethylmethacrylate 10% by weight in the same manner as in Example 1 to block. create a TDI impregnated sheet, the block TDI impregnated melamine resin solution on both sides of the sheet (50 wt%) and 60 g / m polymerized 160 ° C. the glass fiber nonwoven fabric impregnated (basis weight 80 g / m 2) at a ratio of 2 Was molded into a predetermined shape under molding conditions of 3 kg / cm 2 .
上記成形において、シートに含浸されている該ブロック
TDIは加熱によりイソシアナート基を再生し、該共重合
体のアミノ基と反応して急激に硬化する。In the above molding, the block impregnated into the sheet
TDI regenerates the isocyanate group by heating and reacts with the amino group of the copolymer to rapidly cure.
このようにして実施例1同様な内装材が得られる。In this way, an interior material similar to that of Example 1 is obtained.
第1図および第2図は本発明の一実施例を示すものであ
り、第1図はMDI含浸およびエチレングリコール噴霧工
程図、第2図は成形工程図である。 図中、(1)……ポリエーテル型軟質ポリウレタン発泡
シート (9)……ブロックされているMDI溶液 (10)……加熱押圧成形型1 and 2 show one embodiment of the present invention. FIG. 1 is a process drawing of MDI impregnation and ethylene glycol spraying, and FIG. 2 is a molding process drawing. In the figure, (1) …… Polyether type soft polyurethane foam sheet (9) …… Blocked MDI solution (10) …… Heating and pressing mold
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 B29L 31:58 4F ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location B29L 31:58 4F
Claims (4)
イソシアナート化合物を多孔質体に含浸させ、該ブロッ
ク多価イソシアナート化合物の再生温度以上の温度で該
多孔質体を所定形状に加熱成形することを特徴とする内
装材の製造方法。1. A porous body is impregnated with a block polyvalent isocyanate compound that is regenerated at a temperature of 160 ° C. or lower, and the porous body is heated to a predetermined shape at a temperature not lower than the regeneration temperature of the block polyvalent isocyanate compound. A method for manufacturing an interior material, which comprises molding.
定形状に成形することを特徴とする特許請求の範囲1に
記載の内装材の製造方法。2. The method for producing an interior material according to claim 1, wherein a synthetic resin-impregnated paper is polymerized on the porous body to form a predetermined shape.
状に成形することを特徴とする特許請求の範囲1に記載
の内装材の製造方法。3. The method for producing an interior material according to claim 1, wherein a porous reinforcing layer is polymerized on the porous body to be molded into a predetermined shape.
請求の範囲1または2または3に記載の内装材の製造方
法。4. The method for producing an interior material according to claim 1, 2 or 3, wherein the porous body is colored in a predetermined manner.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2085946A JPH0667575B2 (en) | 1990-03-30 | 1990-03-30 | Interior material manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2085946A JPH0667575B2 (en) | 1990-03-30 | 1990-03-30 | Interior material manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03281316A JPH03281316A (en) | 1991-12-12 |
| JPH0667575B2 true JPH0667575B2 (en) | 1994-08-31 |
Family
ID=13872932
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2085946A Expired - Lifetime JPH0667575B2 (en) | 1990-03-30 | 1990-03-30 | Interior material manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0667575B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4415586C1 (en) | 1994-05-03 | 1996-02-08 | Stankiewicz Gmbh | Process for producing a composite foam from foam flakes, composite foam and uses of this composite foam |
-
1990
- 1990-03-30 JP JP2085946A patent/JPH0667575B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03281316A (en) | 1991-12-12 |
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