JPH0247343B2 - PANERUSEIKEIBUTSUNOSEIZOHOHO - Google Patents
PANERUSEIKEIBUTSUNOSEIZOHOHOInfo
- Publication number
- JPH0247343B2 JPH0247343B2 JP57069199A JP6919982A JPH0247343B2 JP H0247343 B2 JPH0247343 B2 JP H0247343B2 JP 57069199 A JP57069199 A JP 57069199A JP 6919982 A JP6919982 A JP 6919982A JP H0247343 B2 JPH0247343 B2 JP H0247343B2
- Authority
- JP
- Japan
- Prior art keywords
- urethane prepolymer
- paper material
- reinforced structure
- adhesive
- curing catalyst
- 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 claims description 42
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 19
- 239000000853 adhesive Substances 0.000 claims description 12
- 230000001070 adhesive effect Effects 0.000 claims description 12
- 238000000465 moulding Methods 0.000 claims description 11
- 239000003054 catalyst Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims 2
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 239000000123 paper Substances 0.000 description 20
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 229920003002 synthetic resin Polymers 0.000 description 6
- 239000000057 synthetic resin Substances 0.000 description 6
- 229920001169 thermoplastic Polymers 0.000 description 5
- 239000004416 thermosoftening plastic Substances 0.000 description 5
- 239000005011 phenolic resin Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 239000002984 plastic foam Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 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 2
- 230000037303 wrinkles Effects 0.000 description 2
- KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000001153 anti-wrinkle effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- KIQKWYUGPPFMBV-UHFFFAOYSA-N diisocyanatomethane Chemical compound O=C=NCN=C=O KIQKWYUGPPFMBV-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Vehicle Interior And Exterior Ornaments, Soundproofing, And Insulation (AREA)
- Laminated Bodies (AREA)
- Paper (AREA)
Description
本発明は例えば自動車の内装基材として賞用さ
れるパネル成形物の製造方法に関するものであ
る。
自動車の内装基材としては従来からダンボール
等の強化構造紙材が用いられている。ダンボール
は安価でかつ軽量であるから自動車内装基材とし
て望ましいものではあるが、所定の形状に成形さ
れた場合に形状保持性に劣り、特に高温では形く
づれが大きい。このような欠点を改良するものと
して、従来、ダンボールにフエノール樹脂等の熱
硬化性合成樹脂やポリエチレン、ポリプロピレン
等の熱可塑性合成樹脂を含浸、あるいは塗布する
方法が提案されている。しかしフエノール樹脂は
硬化温度が180℃以上であり、成形時に高温プレ
スが必要であるから省エネルギー的観点から望ま
しいものではなく、かつ紙質も劣化するおそれが
ある。特にダンボールに耐熱性のない熱可塑性プ
ラスチツクスシートや発泡体、あるいはフエルト
等を重合してダンボールと共に一体成形すること
が不可能になる。また熱可塑性合成樹脂は耐熱性
に乏しくかつ強度に劣るからダンボールの成形安
定性や構造強度が低いものしか得られない。
本発明は上記従来の欠点を改良し、低温成形で
形保持性に優れた強化構造紙材成形物を得ること
を目的とし、強化構造紙材にウレタンプレポリマ
ーを塗布または含浸することを骨子とする。
本発明を以下に詳細に説明する。
本発明に用いられる強化構造紙材とは第1図に
示すように波形芯紙1の両面に表紙2,2を貼着
した構造、第2図に示すように波形芯紙1の片面
に表紙2を貼着した構造、第3図に示すように表
紙2,2の間にハニカム1′を形成した構造等の
あらゆる強化構造を有する紙材を云う。波形芯紙
1やハニカム1′にはフエノール樹脂、尿素樹脂、
メラミン樹脂等が含浸せられていてもよい。
本発明に用いられるウレタンプレポリマーとは
ポリエチレングリコール、ポリプロピレングリコ
ール、ポリエステル等の二個以上のOH基を有す
る長鎖化合物にメチレンジイソシアナート、トリ
レンジイソシアナート等の多価イソシアナート化
合物、または該多価イソシアナート化合物とエチ
レングリコール、グリセリン等の多価アルコー
ル、メチレンジアミン、フエニレンジアミン等の
多価アミン等とのアダクトを反応させてOH基を
NCO基に転換したものを云う。
上記ウレタンプレポリマーは通常は例えばトル
オール、キシロール、メチレンクロライド、トリ
クロルエチレン、酢酸エチル、酢酸ブチル等の活
性酸素を有しない有機溶剤の溶液として提供され
るから、該溶液を強化構造紙材の片面もしくは両
面にスプレー、ロールコーター、ナイフコータ
ー、カーテンフローコーター等で塗布するかもし
くは浸漬法等によつて含浸させ、所望なれば溶剤
の沸点以上の温度によつて乾燥させる。ウレタン
プレポリマーの塗布もしくは含浸量は20〜100
g/m2程度とする。所望なれば該強化構造紙材に
不織布、繊維織編布、フエルト、プラスチツクス
発泡体等のしわ取り材、不織布、繊維織編布、プ
ラスチツクスシート、プラスチツクスシートとプ
ラスチツクス発泡体との重合物等の表装材等の表
材を貼着してもよい。表材の貼着は強化構造紙材
に塗布または含浸したウレタンプレポリマーの硬
化前に行なえば特に接着剤は必要ではないが、ウ
レタンプレポリマーのみでは初期接着強度が小さ
いこと、表材を貼着すると強化構造紙材のウレタ
ンプレポリマー迄湿気もしくは硬化触媒が達し得
ないこと等を考慮して強化構造紙材と表材との接
着には硬化触媒作用を有する接着剤を用いること
が望ましい。硬化触媒作用を有する接着剤とはア
ミノ基、アミド基、カルボキシル基、水酸基等の
活性水素を有する官能基を含む合成樹脂からなる
ものであり、かゝる接着剤をウレタンプレポリマ
ー上に適用すれば該接着剤はウレタンプレポリマ
ーと共同して一体的に硬化する。勿論、活性水素
を有する官能基を含まない合成樹脂からなる接着
剤にアミン、酸アミド、有機酸、アルコール等の
活性水素を含む化合物を硬化触媒として混合して
もよい。素材が多孔質な場合は特に接着剤を用い
ずして表材を通して湿気もしくは硬化触媒をウレ
タンプレポリマーに供給することは可能である。
しかし表材が湿気や硬化触媒によつて変性した
り、また湿気や硬化触媒を含んだ素材を乾燥させ
る工程が余分に必要となる。かくしてウレタンプ
レポリマーを塗布または含浸した強化構造紙材は
単独あるいは表材とともに押圧成形によつて成形
される。ウレタンプレポリマーの硬化は成形直前
に湿気または硬化触媒を強化構造紙材に接触させ
たり、押圧型の型面に設けた孔から蒸気、あるい
は硬化触媒を含む蒸気、あるいは水、あるいは硬
化触媒液を噴出させつゝ成形したりすることによ
つて惹起される。所望なればウレタンプレポリマ
ーを塗布または含浸した強化構造紙材にしわ取り
材を重合し、更に表装材を重合して一体に成形を
行なつてもよい。なお該しわ取り材とは強化構造
紙材の深絞り成形部分の表面に発生するしわが製
品の表面に凹凸となつて発現することを防止する
ものである。
かくして得られたパネル成形物は形保持性が極
めてよく、構造強度もまた大きなものである。
実施例
強化構造紙材10としてフエノール樹脂含浸波
形芯紙1の表面に表面2,2を貼着したダンボー
ルを用いる。
ウレタンプレポリマーとしてポリエチレングリ
コール(重合度3000)にトリレンジイソシアナー
トを反応させたもの(40%メチレンクロライド溶
液)を用いる。
素材としてポリエチレンを接着剤として用いた
熱可塑性フエルトを用いる。
接着剤としてアミノ基を含むアクリル系合成樹
脂(15%プロピレンジクロライド溶液)を用い
る。
第4図においてはダンボール10の両面にロー
ルコーター11A,11Bによつてウレタンプレ
ポリマーを塗布し、次いで該ダンボール10の片
面にスプレーガン12によつて接着剤を塗布し、
その上にロール13から引出した熱可塑性フエル
ト14をロール15によつて圧着し、カツター1
6によつて所定の寸法に裁断しパネル10Aとす
る。
次いで第5図においては上型17A、下型17
Bからなる押圧型17上にパネル10Aを載置し
自動車天井形に押圧成形を行なう。この際、下型
17Bの型面の孔17′から4〜5Kg/m2程度、
約130℃の蒸気を噴出させ、また上型17Aの型
面も130℃程度に加熱する。プレス圧は3〜4
Kg/m2、プレス時間は約10秒とする。かくして強
化構造紙材10と表材14とからなるパネル10
Aが一体的に成形される。成形中強化構造紙材1
0のウレタンプレポリマーは下型17Bからの蒸
気および接着剤によつて硬化される。かくして得
られた自動車天井基材試料は700g/m2と極めて
軽量である。上記試料の熱サイクルテストの結果
を以下に示す。
試料20を下記の熱サイクル下に曝す。
(1) 50℃ 100%RH 8hrs
(2) 80℃ 常 湿 3hrs
(3) −30℃ 〃 3hrs
(1)→(2)→(3)のプロセスを1サイクルとする。
上記熱サイクル試験によつて試料20は第6図
点線のように変形する。該変形の度合hは第1表
に示される。
The present invention relates to a method for producing a panel molded product that is used, for example, as an interior base material for automobiles. Reinforced structural paper materials such as cardboard have traditionally been used as interior base materials for automobiles. Although cardboard is desirable as a base material for automobile interiors because it is inexpensive and lightweight, it has poor shape retention when molded into a predetermined shape, and its shape is significantly distorted, especially at high temperatures. In order to improve these drawbacks, a method has been proposed in the past in which corrugated cardboard is impregnated with or coated with a thermosetting synthetic resin such as a phenol resin, or a thermoplastic synthetic resin such as polyethylene or polypropylene. However, phenolic resin has a curing temperature of 180° C. or higher and requires high-temperature pressing during molding, so it is not desirable from an energy-saving perspective, and there is a risk that the paper quality may deteriorate. In particular, it becomes impossible to polymerize thermoplastic sheets, foams, felt, etc. that do not have heat resistance to the cardboard and integrally mold them together with the cardboard. Furthermore, since thermoplastic synthetic resins have poor heat resistance and strength, only cardboard with low molding stability and low structural strength can be obtained. The present invention aims to improve the above-mentioned conventional drawbacks and obtain a reinforced structural paper material molded product with excellent shape retention through low-temperature molding. do. The invention will be explained in detail below. The reinforced structure paper material used in the present invention has a structure in which covers 2, 2 are pasted on both sides of a corrugated core paper 1 as shown in FIG. 1, and a cover on one side of the corrugated core paper 1 as shown in FIG. 2, or a structure in which a honeycomb 1' is formed between the covers 2 and 2 as shown in FIG. 3. Phenol resin, urea resin,
It may be impregnated with melamine resin or the like. The urethane prepolymer used in the present invention is a long-chain compound having two or more OH groups such as polyethylene glycol, polypropylene glycol, or polyester, and a polyvalent isocyanate compound such as methylene diisocyanate or tolylene diisocyanate. OH groups are produced by reacting adducts of polyvalent isocyanate compounds with polyvalent alcohols such as ethylene glycol and glycerin, and polyvalent amines such as methylene diamine and phenylene diamine.
Refers to those converted to NCO base. The urethane prepolymer is usually provided as a solution in an organic solvent free of active oxygen, such as toluene, xylol, methylene chloride, trichloroethylene, ethyl acetate, butyl acetate, etc. Both sides are coated with a spray, roll coater, knife coater, curtain flow coater, etc., or impregnated by a dipping method, etc., and if desired, dried at a temperature higher than the boiling point of the solvent. The amount of urethane prepolymer applied or impregnated is 20 to 100.
It should be about g/ m2 . If desired, the reinforcing structure paper material may be coated with a wrinkle-removal material such as a non-woven fabric, a fiber-woven knitted fabric, felt, or a plastic foam, a non-woven fabric, a fiber-woven knitted fabric, a plastic sheet, or a polymerization of a plastic sheet and a plastic foam. A surface material such as a surface material for objects etc. may be attached. Adhesion of the surface material does not require any particular adhesive as long as it is done before the urethane prepolymer coated or impregnated on the reinforced structure paper material hardens. However, if the urethane prepolymer alone has low initial adhesive strength, Considering that moisture or the curing catalyst cannot reach the urethane prepolymer of the reinforced structural paper material, it is desirable to use an adhesive having a curing catalytic effect to bond the reinforced structural paper material and the cover material. Adhesives with curing catalytic action are made of synthetic resins containing functional groups with active hydrogen, such as amino groups, amide groups, carboxyl groups, and hydroxyl groups. If so, the adhesive cures integrally with the urethane prepolymer. Of course, a compound containing active hydrogen, such as an amine, an acid amide, an organic acid, or an alcohol, may be mixed as a curing catalyst into an adhesive made of a synthetic resin that does not contain a functional group containing active hydrogen. It is possible to supply moisture or curing catalyst to the urethane prepolymer through the surface material without using an adhesive, especially if the material is porous.
However, the surface material may be denatured by moisture or the curing catalyst, and an extra step is required to dry the material containing moisture or the curing catalyst. The reinforced structure paper material coated or impregnated with the urethane prepolymer is thus molded by pressure molding alone or together with the surface material. The urethane prepolymer is cured by bringing moisture or a curing catalyst into contact with the reinforced structural paper material immediately before molding, or by introducing steam, steam containing a curing catalyst, water, or curing catalyst liquid through holes provided in the mold surface of a pressing mold. It is caused by ejecting and molding. If desired, the reinforced structure paper material coated or impregnated with a urethane prepolymer may be polymerized with the anti-wrinkle material, and then the facing material may be polymerized and integrally formed. The wrinkle removing material is used to prevent wrinkles generated on the surface of the deep-drawn portion of the reinforced structure paper material from appearing as unevenness on the surface of the product. The thus obtained panel molded product has extremely good shape retention and also has high structural strength. Embodiment As the reinforced structure paper material 10, a corrugated cardboard with surfaces 2, 2 attached to the surface of a corrugated core paper 1 impregnated with a phenol resin is used. As the urethane prepolymer, polyethylene glycol (degree of polymerization 3000) reacted with tolylene diisocyanate (40% methylene chloride solution) is used. The material used is thermoplastic felt using polyethylene as an adhesive. Acrylic synthetic resin containing amino groups (15% propylene dichloride solution) is used as the adhesive. In FIG. 4, urethane prepolymer is applied to both sides of a cardboard box 10 using roll coaters 11A and 11B, and then adhesive is applied to one side of the cardboard box 10 using a spray gun 12.
Thermoplastic felt 14 pulled out from roll 13 is crimped onto it by roll 15, and cutter 1
6 to a predetermined size to obtain a panel 10A. Next, in FIG. 5, the upper mold 17A and the lower mold 17
The panel 10A is placed on a pressing die 17 made of B, and press-molded into the shape of an automobile ceiling. At this time, about 4 to 5 kg/m 2 from the hole 17' on the mold surface of the lower mold 17B,
Steam at about 130°C is jetted out, and the mold surface of the upper mold 17A is also heated to about 130°C. Press pressure is 3-4
Kg/m 2 and press time is about 10 seconds. Thus, the panel 10 consisting of the reinforced structural paper material 10 and the facing material 14 is constructed.
A is integrally molded. Reinforced structural paper material during forming 1
The urethane prepolymer No. 0 is cured by steam and adhesive from the lower mold 17B. The thus obtained automobile ceiling base material sample is extremely lightweight at 700 g/m 2 . The results of the thermal cycle test of the above sample are shown below. Sample 20 is subjected to the following thermal cycles. (1) 50℃ 100%RH 8hrs (2) 80℃ Normal humidity 3hrs (3) −30℃ 〃 3hrs The process of (1)→(2)→(3) is one cycle. The sample 20 is deformed as shown by the dotted line in FIG. 6 by the above thermal cycle test. The degree of deformation h is shown in Table 1.
【表】【table】
【表】
第1表によれば本実施例の試料は無処理のダン
ボールを用いた対照1は云うに及ばず、フエノー
ル樹脂強化ダンボールを用いた対照2よりも更に
形安定性に優れる。[Table] According to Table 1, the sample of this example has even better shape stability than Control 1, which uses untreated cardboard, as well as Control 2, which uses phenol resin-reinforced cardboard.
第1図〜第3図は種々な構造の強化構造紙材の
側断面図であり、第4図は押圧成形前の工程図、
第5図は押圧成形時の工程図、第6図は熱サイク
ル試験の変形量を示す側断面図である。
図中10……強化構造紙材、14……表材。
Figures 1 to 3 are side sectional views of reinforced structural paper materials with various structures, and Figure 4 is a process diagram before press molding;
FIG. 5 is a process diagram during press molding, and FIG. 6 is a side sectional view showing the amount of deformation in a thermal cycle test. In the figure, 10... Reinforced structure paper material, 14... Covering material.
Claims (1)
または含浸し、湿気もしくは硬化触媒を該ウレタ
ンポリマーに適用しつゝ押圧成形によつて所望の
形状に成形することを特徴とするパネル成形物の
製造方法。 2 強化構造紙材の両面もしくは片面にウレタン
プレポリマーを塗布または含浸し、両面もしくは
片面には表材を当接した後湿気もしくは硬化触媒
を該ウレタンポリマーに適用しつゝ押圧成形によ
つて所望の形状に成形することを特徴とするパネ
ル成形物の製造方法。 3 特許請求の範囲2において、該強化構造紙材
と該表材とはウレタンプレポリマーの硬化触媒作
用を有する接着剤によつて接着される。[Claims] 1. A reinforced structure paper material is coated with or impregnated with a urethane prepolymer, and moisture or a curing catalyst is applied to the urethane polymer, and the paper material is press-molded into a desired shape. Method for manufacturing panel moldings. 2 Coating or impregnating urethane prepolymer on both sides or one side of the reinforced structure paper material, contacting both sides or one side with a surface material, applying moisture or a curing catalyst to the urethane polymer, and forming the desired shape by press molding. A method for manufacturing a panel molded product, characterized by molding it into a shape. 3. In claim 2, the reinforced structure paper material and the surface material are bonded together with an adhesive having a curing catalytic action of a urethane prepolymer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57069199A JPH0247343B2 (en) | 1982-04-24 | 1982-04-24 | PANERUSEIKEIBUTSUNOSEIZOHOHO |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57069199A JPH0247343B2 (en) | 1982-04-24 | 1982-04-24 | PANERUSEIKEIBUTSUNOSEIZOHOHO |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58185253A JPS58185253A (en) | 1983-10-28 |
| JPH0247343B2 true JPH0247343B2 (en) | 1990-10-19 |
Family
ID=13395813
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57069199A Expired - Lifetime JPH0247343B2 (en) | 1982-04-24 | 1982-04-24 | PANERUSEIKEIBUTSUNOSEIZOHOHO |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0247343B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6036151A (en) * | 1983-08-10 | 1985-02-25 | 三井東圧化学株式会社 | Corrugated cardboard and reinforced corrugated box using said cardboard |
| JPS60224537A (en) * | 1984-04-23 | 1985-11-08 | 三井東圧化学株式会社 | Reinforced corrugated board and reinforced corrugated board vessel using said board |
| JP2001271291A (en) * | 2000-01-20 | 2001-10-02 | Toppan Printing Co Ltd | Impregnated fiber structure and molded article thereof |
-
1982
- 1982-04-24 JP JP57069199A patent/JPH0247343B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58185253A (en) | 1983-10-28 |
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