JPS6248981B2 - - Google Patents
Info
- Publication number
- JPS6248981B2 JPS6248981B2 JP2046982A JP2046982A JPS6248981B2 JP S6248981 B2 JPS6248981 B2 JP S6248981B2 JP 2046982 A JP2046982 A JP 2046982A JP 2046982 A JP2046982 A JP 2046982A JP S6248981 B2 JPS6248981 B2 JP S6248981B2
- Authority
- JP
- Japan
- Prior art keywords
- urethane foam
- foam molded
- molded product
- carbon dioxide
- dioxide gas
- 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
Links
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 48
- 239000006260 foam Substances 0.000 claims description 37
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 36
- 239000001569 carbon dioxide Substances 0.000 claims description 24
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 24
- 239000000126 substance Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000000047 product Substances 0.000 description 57
- 239000011162 core material Substances 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 8
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 210000004027 cell Anatomy 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 229920006337 unsaturated polyester resin Polymers 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- 229920006305 unsaturated polyester Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 229920002430 Fibre-reinforced plastic Polymers 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000011151 fibre-reinforced plastic Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 210000000497 foam cell Anatomy 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000009787 hand lay-up Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 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
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000012783 reinforcing fiber Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Description
本発明はウレタン発泡成形品を使用する製品の
新規な製法に関する。
ウレタン発泡成形品は一般にポリオールとイソ
シアネートの2液を混合する際に水を混和し、発
生する炭酸ガスの膨脹圧により発泡化を行なうこ
とによつて製造されている。したがつて、えられ
るウレタン発泡成形品においては発生した炭酸ガ
スが発泡セル中に残留しており、その残留量は独
立セルが多いほど多い。
かかる炭酸ガスが残留しているウレタン発泡成
形品を使用する製品、たとえばウレタン発泡成形
品を芯材として用いる繊維強化プラスチツクス
(以下、単にFRPという)成形品のばあい、これ
が高温にさらされるとウレタン発泡成形品の芯材
のセル中から逸散してきた炭酸ガスが該芯材と
FRP層との境界に集中し、その結果芯材とFRP
層との間に空洞が形成されてFRP成形品の表面
のフクレとなり、製品の寸法に異常が生じるとい
う問題がある。
かかるフクレを防止する方法として、ウレタン
発泡成形品を50℃前後で長時間加温し、予め炭酸
ガスをセル中から逸散させておく方法や、ウレタ
ン発泡成形品とFRP層との密着性を向上させて
炭酸ガスの膨脹による両者の剥離を物理的に抑制
する方法などが試みられている。しかしこれらの
試みはコストの上昇を招いたり、フクレ防止効果
が不足したり、製品の使用条件が狭い範囲に制限
されるなどの問題がある。
前記においてはウレタン発泡成形品を使用する
製品のフクレの問題をFRP成形品について述べ
たが、その他の樹脂成形品、たとえばポリエチレ
ン、ポリプロピレン、ポリアミド、ABS樹脂な
どの成形品のばあいにも同様な不具合がみられ
る。また乾燥炉などの断熱材としてのウレタン発
泡成形品を鋼板で密閉する構造においても同様の
不具合が発生する。
しかるに本発明者らはウレタン発泡成形品を使
用する製品のフクレを防止する方法について鋭意
検討を重ねた結果、ウレタン発泡成形品にアルカ
リ性物質を存在させることにより熱によりセル中
から放出される炭酸ガスがすみやかに中和されて
液状物質または固体状物質に変化し、気体として
の炭酸ガスが消滅され、その結果フクレの発生が
防止されるという新たな事実を見出して本発明を
完成するに至つた。
すなわち本発明は、ウレタン発泡成形品を実質
的に炭酸ガス不透過性の材料で完全にまたは部分
的に包み込むことからなるウレタン発泡成形品を
使用する製品の製法において、該ウレタン発泡成
形品に炭酸ガスを中和しうるアルカリ性物質を存
在せしめることを特徴とするウレタン発泡成形品
を使用する製品の製法に関する。
しかして本発明においては、ウレタン発泡成形
品にアルカリ性物質を存在させるという簡単な構
成により該ウレタン発泡成形品を使用する製品に
おけるフクレが完全に防止されるので、前述のご
とき従来のフクレ防止法にくらべてコスト面、フ
クレ防止効果、製品の用途面できわめて有利であ
る。
本発明にいうウレタン発泡成形品は、ウレタン
結合を有する高分子化合物の発泡成形品であつ
て、その発泡を主に炭酸ガスに依存するものであ
り、炭酸ガスと他の発泡剤との併用によりえられ
るウレタン発泡成形品も含まれる。また軟質、硬
質いずれの成形品も含まれる。
本発明に用いるアルカリ性物質は炭酸ガスと反
応して液状または固体状物質に変換させうるもの
であればとくに制限されないが、たとえば水酸化
ナトリウム、水酸化カリウムなどのアルカリ金属
水酸化物、水酸化カルシウム、水酸化マグネシウ
ムなどのアルカリ土類金属水酸化物、酸化カルシ
ウム、酸化マグネシウムなどのアルカリ土類金属
酸化物、エチレンジアミン、ジエチレントリアミ
ン、トリエチレンテトラミン、トリメチレンジア
ミン、テトラメチレンジアミン、エタノールアミ
ンなどのアミン類などが用いられる。
前記アルカリ性物質をウレタン発泡成形品に存
在させる方法としては、たとえば該成形品の表面
に直接または該表面に設けた溝に塗布または付着
させる方法、該成形品の内部に直接または内部に
設けた穴に注入する方法などがあげられる。アル
カリ性物質を塗布、付着または注入するに際して
は、アルカリ性物質が固体であれ、液体であれ、
そのまま用いることができ、さらに水または有機
溶剤に分散または溶解して用いることができる。
ウレタン発泡成形品に存在させるアルカリ性物
質の量は用いるウレタン発泡成形品中に存在する
炭酸ガスをほぼ中和しうる量もしくはそれ以上で
あればよい。ウレタン発泡成形品中に存在する炭
酸ガス量は該成形品の発泡倍率などにより変化す
るが、該成形品から一定の大きさの試験片を切り
出してそれについてガスクロマトグラフイーなど
により炭酸ガス量を求め、その値にもとづいてア
ルカリ性物質の使用量を決めることができる。な
おウレタン発泡成形品においては使用する個々の
製品ごとに表皮層や内部層によつて炭酸ガス量が
多少異なるから、最終的には使用するウレタン発
泡成形品ごとにトライアル的に決めるのが望まし
い。
本発明にいうウレタン発泡成形品を使用する製
品は該成形品を実質的に炭酸ガス不透過性の材料
で完全にまたは部分的に包み込んだ構成の製品で
あるが、具体的には自動車のパネルや部品、乾燥
炉の断熱材としてのパネルなどである。前記炭酸
ガス不透過性の材料としてはポリエチレン、ポリ
プロピレン、ポリアミド、ABS樹脂、不飽和ポ
リエステル樹脂などがあげられ、これら樹脂は強
化繊維と併用してもよい。これら樹脂を用いる最
終製品の成形方法としてはハンドレイアツプ法、
スプレーアツプ法、レジンインジエクシヨン法、
射出成形法などが採用される。また炭酸ガス不透
過性材料としては前記樹脂材料以外に鋼、鉄など
の金属板があげられる。
つぎに実施例および比較例をあげて本発明の方
法を説明する。
実施例1〜4および比較例1
硬質ウレタン発泡成形品を芯材に用いてFRP
のレジンインジエクシヨン法により第1〜3図に
示す自動車のバツクドアを作製した。第1図はバ
ツクドアの平面図、第2図は第1図のA―A線拡
大断面図、第3図は第1図のB―B線拡大断面図
である。第1〜3図において、1はウレタン発泡
成形品の芯材、2はFRP層である。
用いた芯材は平均厚さ20mm、全容積10000cm3で
あり、含まれる炭酸ガス量は18gであつた。
レジンインジエクシヨン用FRP製型の下型に
不飽和ポリエステル樹脂(エチレングリコール、
無水マレイン酸およびイソフタル酸からえられた
不飽和ポリエステル100部(重量部、以下同様)、
スチレン30部、メチルエチルケトンパーオキサイ
ド1部、ナフテン酸コバルト0.5部からなるも
の)をスプレー塗布して厚さ0.3mmのゲルコート
層を形成した(えられる最終製品においてこのゲ
ルコート層が外面になる)。ついでこのゲルコー
ト層のうえにガラス繊維のプリフオームおよび第
1表に示されるごとくアルカリ性物質を付与した
芯材(ただし比較例1では付与せず)をセツトし
たのち下型と上型を閉じ、注入孔より不飽和ポリ
エステル樹脂(エチレングリコール、無水マレイ
ン酸および無水フタル酸からえられた不飽和ポリ
エステル100部、スチレン30部、メチルエチルケ
トンパーオキサイド1部からなるもの)を6Kg/
cm2の注入圧で注入し、30分経過後離型し、硬質ウ
レタン発泡成形品を芯材とするFRP製バツクド
アをえた。FRP層の厚さは平均2.5mmとした。
また前記において、芯材に付与するアルカリ性
物質の量は芯材に含まれる炭酸ガス全量(18g)
の中和当量とした。
The present invention relates to a new method for manufacturing products using urethane foam molded products. Urethane foam molded products are generally manufactured by mixing two liquids, polyol and isocyanate, with water, and foaming the mixture under the expansion pressure of the generated carbon dioxide gas. Therefore, in the resulting urethane foam molded product, the generated carbon dioxide gas remains in the foam cells, and the more closed cells there are, the greater the amount remains. In the case of products that use urethane foam molded products in which such carbon dioxide gas remains, such as fiber reinforced plastic (hereinafter simply referred to as FRP) molded products that use urethane foam molded products as a core material, if they are exposed to high temperatures, The carbon dioxide gas escaping from the cells of the core material of the urethane foam molded product interacts with the core material.
concentrated at the boundary between the FRP layer and the resulting core material and FRP
There is a problem in that cavities are formed between the layers, causing blisters on the surface of the FRP molded product, and causing abnormalities in the dimensions of the product. Methods to prevent such blistering include heating the urethane foam molded product for a long time at around 50°C to dissipate carbon dioxide gas from the cells in advance, and improving the adhesion between the urethane foam molded product and the FRP layer. Attempts have been made to improve this and physically suppress the separation of the two due to expansion of carbon dioxide gas. However, these attempts have problems such as increased cost, lack of blistering prevention effect, and limited use conditions of the product. In the above, the problem of blistering in products using urethane foam molded products was discussed with respect to FRP molded products, but the same problem also applies to molded products of other resins, such as polyethylene, polypropylene, polyamide, ABS resin, etc. There is a problem. A similar problem also occurs in a structure in which a urethane foam molded product used as a heat insulating material in a drying oven is sealed with a steel plate. However, as a result of extensive research into ways to prevent blistering in products using urethane foam molded products, the present inventors found that by adding an alkaline substance to the urethane foam molded product, carbon dioxide gas released from the cells due to heat can be prevented. The present invention was completed by discovering a new fact that carbon dioxide gas is quickly neutralized and changed into a liquid or solid substance, and gaseous carbon dioxide is eliminated, thereby preventing the occurrence of blisters. . That is, the present invention provides a method for producing a product using a urethane foam molded product, which comprises completely or partially wrapping the urethane foam molded product with a material that is substantially impermeable to carbon dioxide. The present invention relates to a method for producing a product using a urethane foam molded product, which is characterized by the presence of an alkaline substance capable of neutralizing gas. However, in the present invention, blistering in products using the urethane foam molded product can be completely prevented by a simple configuration in which an alkaline substance is present in the urethane foam molded product. It is extremely advantageous in terms of cost, anti-blister effect, and product usage. The urethane foam molded product referred to in the present invention is a foam molded product of a polymer compound having urethane bonds, and its foaming is mainly dependent on carbon dioxide gas, and by using carbon dioxide gas and other blowing agents in combination. It also includes urethane foam molded products. It also includes both soft and hard molded products. The alkaline substance used in the present invention is not particularly limited as long as it can react with carbon dioxide gas and convert into a liquid or solid substance, but examples include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide, and calcium hydroxide. , alkaline earth metal hydroxides such as magnesium hydroxide, alkaline earth metal oxides such as calcium oxide and magnesium oxide, amines such as ethylenediamine, diethylenetriamine, triethylenetetramine, trimethylenediamine, tetramethylenediamine, and ethanolamine. etc. are used. The alkaline substance may be present in the urethane foam molded product, for example, by applying or adhering it directly to the surface of the molded product or in a groove provided on the surface, or by applying it directly to the inside of the molded product or through a hole provided therein. Examples include methods of injecting into When applying, attaching or injecting alkaline substances, whether the alkaline substance is solid or liquid,
It can be used as it is, or it can be dispersed or dissolved in water or an organic solvent. The amount of the alkaline substance present in the urethane foam molded product may be an amount that can substantially neutralize carbon dioxide gas present in the urethane foam molded product or more. The amount of carbon dioxide gas present in a urethane foam molded product varies depending on the foaming ratio of the molded product, etc., but a test piece of a certain size is cut out from the molded product and the amount of carbon dioxide gas is determined by gas chromatography etc. , the amount of alkaline substances to be used can be determined based on that value. Note that in urethane foam molded products, the amount of carbon dioxide gas varies somewhat depending on the skin layer and inner layer of each product used, so it is desirable to ultimately decide on a trial basis for each urethane foam molded product to be used. The product using the urethane foam molded product according to the present invention is a product in which the molded product is completely or partially wrapped in a material that is substantially impermeable to carbon dioxide, and specifically, it is used for automobile panels. and parts, and panels used as insulation for drying ovens. Examples of the carbon dioxide impermeable material include polyethylene, polypropylene, polyamide, ABS resin, and unsaturated polyester resin, and these resins may be used in combination with reinforcing fibers. The molding methods for final products using these resins include hand lay-up method,
Spray up method, resin injection method,
Injection molding methods are used. In addition to the above-mentioned resin materials, examples of carbon dioxide impermeable materials include metal plates such as steel and iron. Next, the method of the present invention will be explained with reference to Examples and Comparative Examples. Examples 1 to 4 and Comparative Example 1 FRP using hard urethane foam molded product as core material
The back door of an automobile shown in FIGS. 1 to 3 was manufactured by the resin injection method described above. 1 is a plan view of the back door, FIG. 2 is an enlarged sectional view taken along the line AA in FIG. 1, and FIG. 3 is an enlarged sectional view taken along the line BB in FIG. 1. In Figures 1 to 3, 1 is the core material of the urethane foam molded product, and 2 is the FRP layer. The core material used had an average thickness of 20 mm, a total volume of 10,000 cm 3 , and contained 18 g of carbon dioxide gas. The lower mold of the FRP mold for resin injection molding is made of unsaturated polyester resin (ethylene glycol,
100 parts (parts by weight, same hereinafter) of unsaturated polyester obtained from maleic anhydride and isophthalic acid,
30 parts of styrene, 1 part of methyl ethyl ketone peroxide, and 0.5 parts of cobalt naphthenate) was spray applied to form a 0.3 mm thick gel coat layer (this gel coat layer will be the outer surface of the resulting final product). Next, on top of this gel coat layer, a glass fiber preform and a core material to which an alkaline substance was added as shown in Table 1 (but not in Comparative Example 1) were set, and the lower mold and upper mold were closed, and the injection hole was closed. 6 kg of a more unsaturated polyester resin (consisting of 100 parts of an unsaturated polyester obtained from ethylene glycol, maleic anhydride and phthalic anhydride, 30 parts of styrene, and 1 part of methyl ethyl ketone peroxide)
It was injected at an injection pressure of cm 2 and released from the mold after 30 minutes to obtain an FRP back door with a hard urethane foam molded product as the core material. The average thickness of the FRP layer was 2.5 mm. In addition, in the above, the amount of alkaline substance added to the core material is the total amount of carbon dioxide contained in the core material (18g)
The neutralization equivalent of
【表】
えられた各バツクドアを80℃で8時間加熱した
ところ、アルカリ性物質を付与した実施例1〜4
では芯材とFRP層との界面にフクレが認められ
なかつたが、アルカリ性物質を付与しない比較例
1では第4図(第2図に対応)および第5図(第
3図に対応)に示すごとくフクレが発生した。そ
のフクレの程度〔第4〜5図に示される分離した
芯材とFRP層との最大距離H〕は約10mmであつ
た。
実施例5〜8および比較例2
実施例1〜4で用いたと同じ硬質ウレタン発泡
成形品(厚さ40mm)を厚さ0.5mmの鋼板で包み込
んで乾燥炉用のパネルを作製した。実施例5〜8
におけるアルカリ性物質の種類、使用状態、付与
方法はそれぞれ実施例1〜4と同様とした(ただ
し比較例2ではアルカリ性物質を付与しなかつ
た)。
えられた各パネルを100℃で10時間加熱したと
ころ、実施例5〜8ではフクレがまつたく認めら
れなかつたが、比較例2ではフクレが発生し、そ
のフクレの程度は約5mmであつた。[Table] Examples 1 to 4 in which the obtained backdoors were heated at 80°C for 8 hours and an alkaline substance was added.
In Comparative Example 1, no blistering was observed at the interface between the core material and the FRP layer, but as shown in Figure 4 (corresponding to Figure 2) and Figure 5 (corresponding to Figure 3), Comparative Example 1 did not contain any alkaline substances. A lot of blisters occurred. The degree of blistering [the maximum distance H between the separated core material and the FRP layer shown in FIGS. 4 and 5] was about 10 mm. Examples 5 to 8 and Comparative Example 2 The same rigid urethane foam molded product (40 mm thick) used in Examples 1 to 4 was wrapped in a 0.5 mm thick steel plate to produce a panel for a drying oven. Examples 5-8
The type of alkaline substance, usage conditions, and application method were the same as in Examples 1 to 4 (however, in Comparative Example 2, no alkaline substance was applied). When each of the resulting panels was heated at 100°C for 10 hours, no blisters were observed in Examples 5 to 8, but blisters occurred in Comparative Example 2, and the extent of the blisters was approximately 5 mm. .
第1図はウレタン発泡成形品を芯材とする
FRP製バツクドアの平面図、第2図は第1図の
A―A線拡大断面図、第3図は第1図のB―B線
拡大断面図、第4図および第5図は該バツクドア
の加熱後のフクレの状態を示す断面図であり、そ
れぞれ第2図および第3図に対応する。
図面の主要符号、1:ウレタン発泡成形品の芯
材、2:FRP層。
Figure 1 uses a urethane foam molded product as the core material.
A plan view of the FRP back door, Fig. 2 is an enlarged sectional view taken along the line AA in Fig. 1, Fig. 3 is an enlarged sectional view taken along the line B-B in Fig. 1, and Figs. 4 and 5 show the back door. FIG. 3 is a cross-sectional view showing the state of blisters after heating, and corresponds to FIG. 2 and FIG. 3, respectively. Main symbols in the drawing: 1: Core material of urethane foam molded product, 2: FRP layer.
Claims (1)
過性の材料で完全にまたは部分的に包み込むこと
からなるウレタン発泡成形品を使用する製品の製
法において、該ウレタン発泡成形品に炭酸ガスを
中和しうるアルカリ性物質を存在せしめることを
特徴とするウレタン発泡成形品を使用する製品の
製法。1. In a method for manufacturing a product using a urethane foam molded product, which consists of completely or partially wrapping the urethane foam molded product with a material that is substantially impermeable to carbon dioxide gas, the urethane foam molded product is neutralized with carbon dioxide gas. A method for producing a product using a urethane foam molded product, which is characterized by the presence of a potentially alkaline substance.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2046982A JPS58138738A (en) | 1982-02-10 | 1982-02-10 | Production of article using urethane foamed moldings |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2046982A JPS58138738A (en) | 1982-02-10 | 1982-02-10 | Production of article using urethane foamed moldings |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58138738A JPS58138738A (en) | 1983-08-17 |
| JPS6248981B2 true JPS6248981B2 (en) | 1987-10-16 |
Family
ID=12027950
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2046982A Granted JPS58138738A (en) | 1982-02-10 | 1982-02-10 | Production of article using urethane foamed moldings |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58138738A (en) |
-
1982
- 1982-02-10 JP JP2046982A patent/JPS58138738A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58138738A (en) | 1983-08-17 |
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