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JPS63126981A - Production of automotive interior material - Google Patents

Production of automotive interior material

Info

Publication number
JPS63126981A
JPS63126981A JP61268170A JP26817086A JPS63126981A JP S63126981 A JPS63126981 A JP S63126981A JP 61268170 A JP61268170 A JP 61268170A JP 26817086 A JP26817086 A JP 26817086A JP S63126981 A JPS63126981 A JP S63126981A
Authority
JP
Japan
Prior art keywords
adhesive
epoxy resin
resin
emulsion
base material
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP61268170A
Other languages
Japanese (ja)
Inventor
Seinosuke Horiki
堀木 清之助
Kuninori Ito
邦矩 伊藤
Nobuhiko Kinooka
宣彦 紀岡
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nagoya Oil Chemical Co Ltd
Original Assignee
Nagoya Oil Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nagoya Oil Chemical Co Ltd filed Critical Nagoya Oil Chemical Co Ltd
Priority to JP61268170A priority Critical patent/JPS63126981A/en
Publication of JPS63126981A publication Critical patent/JPS63126981A/en
Pending legal-status Critical Current

Links

Landscapes

  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
  • Laminated Bodies (AREA)
  • Lining Or Joining Of Plastics Or The Like (AREA)

Abstract

PURPOSE:To obtain the titled interior material having excellent heat resistance, by sticking base material of the interior material and a surfacing material together with an adhesive mainly containing a mixture of emulsion type adhesive and epoxy resin. CONSTITUTION:A base material such as resin board, high density foam urethane, etc., and a surfacing material (e.g. polyvinylchloride leather, laminate obtained by lining a nonwoven to a leather, etc.) are stuck together with an adhesive prepared by adding a curing agent such as an aliphatic polyamine, isocyanate (for said emulsion resin), etc., to a mixture of an emulsion type adhesive, e.g. natural rubber, synthetic rubber latex or (meth)arylic acid ester based elusion and epoxy resin to provide the aimed automotive interior material having extremely excellent heat resistance. The epoxy resin includes a condensate obtained by reaction of epichlorohydrin with bisphenols, etc.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は天井材、ドアトリム、リヤボード、リヤトレー
、トランクルームの壁材、座席シートあるいは床材等に
用いられる自動車内装材の製造方法に関するものである
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a method for manufacturing automobile interior materials used for ceiling materials, door trims, rear boards, rear trays, trunk wall materials, seat sheets, floor materials, etc. .

〔発明の背景〕[Background of the invention]

この種の内装材はレジンボード、高密度発泡ウレタン、
ダンボール、ポリスチレン発泡体パネル。
This type of interior material is resin board, high-density foamed urethane,
Cardboard, polystyrene foam panels.

ハードボード、プラスチックパネル等からなる基材にポ
リ塩化ビニルレザー、ポリ塩化ビニルレザーとポリウレ
タン発泡体シートとの積層材、不織布、繊維編織物等の
表装材を貼合わせることによシ製造される。
It is manufactured by laminating a covering material such as polyvinyl chloride leather, a laminate of polyvinyl chloride leather and polyurethane foam sheet, nonwoven fabric, or textile knitted fabric to a base material such as hardboard or plastic panel.

〔従来の技術〕[Conventional technology]

従来は上記内装材の製造において基材と表装材との貼合
わせには主として感熱性接着剤や二液硬化溶剤型接着剤
が用いられていた。
Conventionally, heat-sensitive adhesives and two-component curing solvent-based adhesives have been mainly used to bond base materials and facing materials together in the production of interior materials.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかし感熱性接着剤を用いた場合には耐熱性に問題があ
り、二液硬化溶剤型接着剤を用いた場合には硬化剤を接
着剤に混合した状態ではボートライフが短かく、また有
機溶剤を用いるために毒性引火性等の心配もある。
However, when heat-sensitive adhesives are used, there are problems with heat resistance, when two-component curing solvent-based adhesives are used, the boat life is short when a curing agent is mixed with the adhesive, and when organic solvents are used, the boat life is short. There are also concerns about toxicity and flammability due to the use of

〔問題点を解決するだめの手段〕[Failure to solve the problem]

本発明は上記従来の問題点を解決する手段として、エマ
ルジョン型接着剤と、エポキシ樹脂との混合物を主体と
した接着剤を用いて基材と表装材とを貼合わせるもので
ある。
The present invention solves the above-mentioned conventional problems by bonding a base material and a facing material using an adhesive mainly composed of a mixture of an emulsion type adhesive and an epoxy resin.

本発明に用いられるエマルジョン型接着剤としては、例
えば天然ゴム、スチレンーブタジエンゴム、スチレン−
ブタジェンブロー り共w合体、スチレンーイソプレン
ブローク共重合体、アクリロニトリル−ブタジェンゴム
、インプレンゴム、クロロプレンゴム、ブチルブム、ケ
リイソブチレンゴム、ポリブテンゴム、クラフトゴム等
の天然コムもしくは合成ゴムのラテサクス、アクリル酸
エステル系樹脂、メタクリル酸エステル系樹脂、酢酸ビ
ニル系樹脂、プロピオン酸ビニル系樹脂、酢酸ビニル−
エチレン共重合体系樹脂、酢酸ビニル−マレイン酸共重
合体系樹脂、スチレン系樹脂。
Examples of emulsion adhesives used in the present invention include natural rubber, styrene-butadiene rubber, and styrene-butadiene rubber.
Latex of natural or synthetic rubber such as butadiene blow copolymer, styrene-isoprene blow copolymer, acrylonitrile-butadiene rubber, imprene rubber, chloroprene rubber, butyl rubber, kerriisobutylene rubber, polybutene rubber, kraft rubber, acrylic acid ester resins, methacrylate ester resins, vinyl acetate resins, vinyl propionate resins, vinyl acetate resins
Ethylene copolymer resin, vinyl acetate-maleic acid copolymer resin, styrene resin.

塩化ビニル系樹脂、塩化ビニル−エチレン共重合体系樹
脂、塩化ビニル−酢酸ビニル共重合体系樹脂、塩化ビニ
リデン系樹脂、ポリビニルエーテル系樹脂等の合成樹脂
エマルジョンである。そして上記合成ゴムラテ・クスお
よび合成樹脂エマルジョンはカルボキシル基、水酸基、
メチロール基。
These are synthetic resin emulsions such as vinyl chloride resins, vinyl chloride-ethylene copolymer resins, vinyl chloride-vinyl acetate copolymer resins, vinylidene chloride resins, and polyvinyl ether resins. The synthetic rubber latex and synthetic resin emulsion have carboxyl groups, hydroxyl groups,
Methylol group.

アミノ基、酸アミド基等のエポキシ基と反応可能な官能
基を有することが望ましい。上記合成ゴムラテークスお
よび合成樹脂エマルジョンは二種以上混合されてもよい
It is desirable to have a functional group capable of reacting with an epoxy group such as an amino group or an acid amide group. Two or more kinds of the above synthetic rubber latex and synthetic resin emulsion may be mixed.

更に本発明の接着剤にはロジン、石油樹脂、クマロン樹
脂、ロジン誘導体、テルペン系樹脂、フェノール系樹脂
、アルキルフェノール糸樹脂等の粘着付与剤、) /レ
オール、キジロール、酢酸エチw、酢en−ブチル、メ
チルエチルケトン、メチルインブチルケトン、セロソル
ブアセテート、n−ブチルセロソルブ、エチレングリコ
ール、ジエチレングリコール、プロピレングリコール、
クリセリン、ポリエチレングリコール、ポリプロピレン
グリコール等の有機溶剤もしくは湿潤剤、クレー、タル
ク、ベントナイト、炭酸カルシウム等の充填剤等が添加
されてもよい。
Furthermore, the adhesive of the present invention includes tackifiers such as rosin, petroleum resin, coumaron resin, rosin derivative, terpene resin, phenol resin, alkylphenol thread resin, etc. , methyl ethyl ketone, methyl imbutyl ketone, cellosolve acetate, n-butyl cellosolve, ethylene glycol, diethylene glycol, propylene glycol,
Organic solvents or wetting agents such as chrycerin, polyethylene glycol, polypropylene glycol, fillers such as clay, talc, bentonite, calcium carbonate, etc. may be added.

本発明に用いられるエポキシ樹脂とけエポキシ基を有す
る合成樹脂全搬を言い、このようなエポキシ樹脂として
はエピクロルヒドリンとビスフェノール類および/また
は多価アルコールとの反応により得られる縮合体、グリ
シジルメタクリレート、グリシジルアクリレート、グリ
シジルアリルエーテル等のエポキシ基含有ビニル単量体
を共重合しだ共重合体等が例示される。該エポキシ樹脂
バドルオール、キジロール、酢酸エチル、酢酸n−ブチ
μ、メチルエチルケトン、メチルインブチルケトン、セ
ロソルブアセテート、エチルセロソルブ、n−ブチルセ
ロソルブ等の有機溶剤mH1あるいはエマルジョンの形
状で提供される。
The epoxy resin used in the present invention refers to all synthetic resins having epoxy groups, and such epoxy resins include condensates obtained by reacting epichlorohydrin with bisphenols and/or polyhydric alcohols, glycidyl methacrylate, and glycidyl acrylate. Examples include copolymers obtained by copolymerizing epoxy group-containing vinyl monomers such as , glycidyl allyl ether, and the like. The epoxy resin is provided in the form of an organic solvent mH1 or an emulsion such as badrol, quidylol, ethyl acetate, n-butyl acetate, methyl ethyl ketone, methyl imbutyl ketone, cellosolve acetate, ethyl cellosolve, n-butyl cellosolve.

エマルジョン型接着剤とエポキシ樹脂との混合比率は任
意でよいが、一般には該接着剤とエポキシ樹脂との重量
比率は固形分として98:2〜65:35程度が望まし
い。何となればエポキシ樹脂の比率が上記範囲を下回れ
ば耐熱性接着力が低下し、上記範囲を」二回ればボート
ライフが短かくなる。
Although the mixing ratio of the emulsion type adhesive and the epoxy resin may be arbitrary, it is generally desirable that the weight ratio of the adhesive and the epoxy resin is about 98:2 to 65:35 in terms of solid content. If the ratio of epoxy resin is below the above range, the heat-resistant adhesive strength will decrease, and if it exceeds the above range twice, the life of the boat will be shortened.

上記成分以外、本発明の接着剤には脂肪族ポリアミン、
ヘキザメチレンジアミンカーバメート。
In addition to the above components, the adhesive of the present invention includes aliphatic polyamine,
Hexamethylene diamine carbamate.

安息香酸アンモニウム、酸無水物等のエポキシ樹脂硬化
剤、ジイソシアナート、メラミン樹脂等のエマルジョン
型接着剤の硬化剤、ポリビニルアルコール、メチルセル
ロース、カルボキシメチルセルロース、ヒドロキシメチ
ルセルロース、is>。
Epoxy resin hardeners such as ammonium benzoate and acid anhydrides, hardeners for emulsion adhesives such as diisocyanates and melamine resins, polyvinyl alcohol, methyl cellulose, carboxymethyl cellulose, hydroxymethyl cellulose, IS>.

変性澱粉、顔料、染料、老化防止剤、酸化防止剤等が添
加されてもよい。エポキシ樹脂硬化剤の量は通常エポキ
シ樹脂の固形分に対して10〜40重量%とする。
Modified starch, pigments, dyes, antiaging agents, antioxidants, etc. may be added. The amount of the epoxy resin curing agent is usually 10 to 40% by weight based on the solid content of the epoxy resin.

本発明の基材としてはレジンボード、高密度発泡ウレタ
ン、ダンボール、ポリスチレン発泡体パネル、ハードボ
ード、ポリプロピレン、ポリ塩化ビニル、アクリロニト
リル−ブタジェン−スチレン共重合体等のプラスチ〜り
のパネル等が用いられ、本発明の表装材としてはポリ塩
化ビニル、ポリアミド、ポリウレタン等からなるレザー
、あるいけ該レザーに不織布、繊維編織物、ポリエチレ
ン発泡体、ポリ4化ビニル発泡体、ポリウレタン発泡体
等のり9ジヨン材を裏打ちした積層材、不織布、繊維編
織物等が用いられる。
As the base material of the present invention, resin boards, high-density urethane foam, cardboard, polystyrene foam panels, hardboards, polypropylene, polyvinyl chloride, plastic panels such as acrylonitrile-butadiene-styrene copolymers, etc. are used. The facing material of the present invention is a leather made of polyvinyl chloride, polyamide, polyurethane, etc., or the leather is coated with a glue material such as a nonwoven fabric, a fiber knitted fabric, a polyethylene foam, a polyvinyl tetrachloride foam, a polyurethane foam, etc. Laminated materials, non-woven fabrics, fiber knitted fabrics, etc., are used.

本発明の基材は所望なれば予め所定形状に成形され、そ
れから該基材表面および/または該表装材裏面に本発明
の接着剤を塗布し、所望なれば予備乾燥した後基材と表
装材とが貼合せられる。基材と表装材との貼合せにはホ
、ドブレス、コールドプレス、真空成形等が適用される
。所望なれば基材と表装材とを貼合せるのと同時に成形
が行われてもよいし、基材と表装材とを貼合せた後に成
形が行われてもよい。
The base material of the present invention is formed into a predetermined shape in advance, if desired, and then the adhesive of the present invention is applied to the surface of the base material and/or the back surface of the facing material, and if desired, after pre-drying, the base material and the facing material are are pasted together. For bonding the base material and the facing material, methods such as holstering, doweling, cold pressing, vacuum forming, etc. are applied. If desired, molding may be performed at the same time as bonding the base material and the facing material, or may be performed after bonding the base material and the facing material.

〔作 用〕[For production]

エマルジョン型接着剤にエポキシ樹脂あるいはその硬化
剤を混合した場合、混合物中においてはエマルジョン型
接着剤を構成する合成樹脂またはゴム、あるいはエポキ
シ樹脂や硬化剤は界面活性剤のミセル中に包含されてい
るから相互に分子的な接触は生じない。したがって混合
物のボートライフ、即ち可使時間は長くなる。接着後は
水分の蒸発によシ接着剤はフィルム化し、該フィルム中
において1は核合成樹脂またはゴム、エポキシ樹脂ある
いけ硬化剤は分子的に接触し硬化する。
When an epoxy resin or its curing agent is mixed with an emulsion-type adhesive, the synthetic resin or rubber constituting the emulsion-type adhesive, or the epoxy resin and curing agent are contained in micelles of surfactant. No mutual molecular contact occurs between the two. The boat life, or pot life, of the mixture is therefore increased. After adhesion, moisture evaporates and the adhesive forms a film. In the film, 1 is a nuclear synthetic resin or rubber, and the epoxy resin or curing agent is brought into molecular contact and cured.

〔発明の効果〕〔Effect of the invention〕

したがって本発明においては接着剤はエマlレジコン型
であるから毒性や引火性の心配がなく、また可使時間が
長いから作業工程が合理化され、更に硬化後は耐熱性の
極めて良好な接着が得られ、自動車内装材に用いられる
天井材、ドア)IJム。
Therefore, in the present invention, since the adhesive is of the emul resin type, there is no need to worry about toxicity or flammability, and the work process is streamlined because the pot life is long, and furthermore, after curing, an adhesive with extremely good heat resistance can be obtained. Ceiling materials used in automobile interior materials, door) IJ.

リヤボード、リヤトレー、座席シート、トランクルーム
トリムや壁材あるいは床材等を製造する接着剤として非
常に有用である。
It is very useful as an adhesive for manufacturing rear boards, rear trays, seats, trunk trim, wall materials, floor materials, etc.

実施例1゜ 酢酸ビニlしニアクリル酸エチル:アクリロニトリルが
60:80:10重量比である共重合体からなる50重
量%(以下単に%とする)エマルジョン90重量部(以
下単に部とする)と、エピクロルヒドリンとビスフェノ
−A/Aとの縮合体からなる50%エポキシエマルジョ
ン10部トヲ混合し、更に硬化剤としてポリアミンを1
.5部混合して接着剤Aを調整する。該接着剤Aをドア
トリムの基材として使用するレジンボードに80g/W
l(Dry)の塗布量で塗布し、80’CX5分乾燥さ
せた後、ポリ塩化ビニルレザーに不織布を裏打ちした積
層表装材ヲ重ネ0.8 kg/cyt2.80”CX 
l 分0真空成形によシ貼合せた。また硬化剤添加後の
経過時間による接着剤Aの粘度変化と接着力の変化も合
せて行った結果を第1表に示す。
Example 1 90 parts by weight (hereinafter simply referred to as parts) of a 50% by weight (hereinafter simply referred to as %) emulsion consisting of a copolymer of vinyl acetate and ethyl diacrylate: acrylonitrile in a weight ratio of 60:80:10. , 10 parts of a 50% epoxy emulsion consisting of a condensate of epichlorohydrin and bispheno-A/A were mixed, and 1 part of a polyamine was added as a curing agent.
.. Prepare Adhesive A by mixing 5 parts. Adhesive A was applied to the resin board used as the base material for the door trim at 80g/W.
1 (Dry), and after drying for 5 minutes at 80'CX, apply a laminated covering material made of polyvinyl chloride leather lined with non-woven fabric.
It was laminated by vacuum forming for 0 minutes. Table 1 also shows the results of changes in the viscosity and adhesive strength of Adhesive A depending on the elapsed time after addition of the curing agent.

第1表 △はポリ塩化ビニルレザーの破断 木、常態:貼合せ後室温で24時間放置後の強度床2I
T1熱:貼合せ後室温で24時間放置後、80’CX8
時間放置後の強度 木8耐水:貼合せ後室温で24時間放置後20’Cの水
中に24時間浸漬後の強度 実施例2゜ 酢酸ビニル−エチレン共重合体からなる50%エマルジ
ョン80部に45%テルペン樹脂エマルジョン20部と
実施例1による50%エポキシエマルジョン20部とを
混合し、更に硬化剤としてポリアミド4部を混合して接
着剤Bを調整する。
Table 1 △ shows broken wood of polyvinyl chloride leather, normal condition: strength floor 2I after being left at room temperature for 24 hours after lamination
T1 heat: After lamination and left at room temperature for 24 hours, 80'CX8
Strength after standing for hours Wood 8 Water resistance: After lamination, left at room temperature for 24 hours, strength after immersion in water at 20'C for 24 hours Example 2: 45% in 80 parts of a 50% emulsion consisting of vinyl acetate-ethylene copolymer Adhesive B is prepared by mixing 20 parts of the 50% terpene resin emulsion and 20 parts of the 50% epoxy emulsion according to Example 1, and further mixing 4 parts of polyamide as a curing agent.

該接着剤Bをリヤーボードの基材として使用するハート
ボードおよび表装材としてのニードルパンチカーベート
の両面K 80 g/mの塗布量で塗布した後、80℃
×5分乾燥さセ1.0 kg/ax2.90℃X 0.
5分のホットプレスによシ貼合せた。このものの接着力
を実施例1と同様にして測定した結果を第2表に示す。
The adhesive B was applied to both sides of the heart board used as the base material of the rear board and the needle punch carbate used as the facing material at a coating amount of K 80 g/m, and then heated at 80°C.
Dry for 5 minutes at 1.0 kg/ax at 2.90°C x 0.
It was laminated by hot pressing for 5 minutes. The adhesive strength of this product was measured in the same manner as in Example 1, and the results are shown in Table 2.

第2表 水、耐老化:貼合せ後、室温で24時間放置後80’C
X20日熱老化後の強度 実施例3゜ 50%ポリクロロプレンエマルジョン80部にエピクロ
ルヒドリンとビスフェノ−/l/Al/エトレングリコ
ールとの共縮合物の50%エポキシエマルジョン15部
および0.5%カルボキシメチA/セルローズ8部、青
色染料0001部を加え、更に硬化剤としてポリアミド
を3.5部加え、混合して接着剤Cを調整する、該接着
剤Cを天井利の基材に使用するポリスチレン発泡体に1
20 g/d(Dry)の塗布量で塗布し、70°CX
5分乾燥させた後、不織布と発泡ポリエチレンとの積層
表装材を重ね、0.6 kg /1yn2の圧力でコー
ルドプレスさせ貼合せた後、成形したものは常態はもち
ろん90’CX500hrの熱老化および50°cX9
8%RHX500hrの耐湿試験でもはがれやフクレ、
埼たその他の異状はみられなかった。
Second surface water, aging resistance: 80'C after lamination and left at room temperature for 24 hours
Strength after heat aging for 20 days Example 3 80 parts of a 50% polychloroprene emulsion, 15 parts of a 50% epoxy emulsion of a cocondensate of epichlorohydrin and bisphenol/l/Al/ethrene glycol and 0.5% carboxymethyA / Add 8 parts of cellulose, 0001 parts of blue dye, and further add 3.5 parts of polyamide as a hardening agent and mix to prepare adhesive C. Polystyrene foam using adhesive C as a base material for ceiling adhesive. to 1
Apply with a coating amount of 20 g/d (Dry) and heat at 70°C
After drying for 5 minutes, the laminated surface material of non-woven fabric and foamed polyethylene was layered and bonded together by cold pressing at a pressure of 0.6 kg/1yn2. 50°cX9
Even in the 8%RHX500hr humidity test, there was no peeling or blistering.
No other abnormalities were observed.

実施例4゜ 60%スチレンーブタジエンゴムラテ呼クスり0部に5
0%フェノール樹脂エマルジョン10部およびグリシジ
ルメタクリレートの20%を含有するアクリ/l/共重
合体からなる50%エマルジョン30部を混合し、更に
無水マレイン酸0.9部を混合して接着剤りを調整する
。該接着剤りを基材として座席シートに使用する成型さ
れた高密度発泡ウレタンホームに120g/y&の塗布
量で塗布後縁物を重ね80°CX5分乾燥、貼合せた。
Example 4 60% styrene-butadiene rubber latte 0 parts to 5 parts
10 parts of a 0% phenolic resin emulsion and 30 parts of a 50% emulsion of acrylic/l/copolymer containing 20% of glycidyl methacrylate were mixed, and 0.9 part of maleic anhydride was further mixed to form an adhesive. adjust. Using the adhesive as a base material, a molded high-density foamed urethane foam to be used for a seat sheet was coated with a coating amount of 120 g/y, and then the edges were layered, dried at 80° C. for 5 minutes, and bonded.

このものの接着力試験結果を第3表に示す。Table 3 shows the adhesive strength test results of this product.

第8表 実施例5゜ 実施例2に用いた酢酸ビニル−エチレン共重合の50%
エマルジョンに対し、50%エポキシエマルジョンとの
混合比率を第4表に示すように種々変えたものを接着剤
として用い、基材としてのレジンボード側に100 g
/m (Dry)で塗布した後、80°CXl0分間乾
燥させ、発泡ポリ塩化ビニルシートを重ね0.7 tc
q/al’ 、 s o°CXI分ホ咋ドブレスによっ
て貼合せたものの接着力、および硬化剤添加後の粘度変
化を第5表に示す。
Table 8 Example 5゜50% of vinyl acetate-ethylene copolymerization used in Example 2
The emulsion was mixed with 50% epoxy emulsion at various mixing ratios as shown in Table 4, and 100 g was applied to the resin board as the base material.
/m (Dry), dried at 80°C for 0 minutes, and covered with a foamed polyvinyl chloride sheet for 0.7 tc.
Table 5 shows the adhesion strength of the samples laminated by q/al', so°CXI, and the viscosity change after addition of the curing agent.

尚、硬化剤としてはポリアミドをエポキシ樹脂に対し1
5%添加した。
In addition, as a curing agent, polyamide is used in a ratio of 1 part to epoxy resin.
Added 5%.

第4表 本、常1嘘:貼合せ後室温で24時間放置後の接着力 *6耐熱:貼合せ後室温で24時間放置後80°Cで3
時間放置後の接着力 *7耐熱老化:貼合せ後室温で24時間放置後80°C
で20日間放置後の接着力 東、耐水性:貼合せ後室温で24時間放置後20°Cの
水中に24時間浸漬後の接着力 実施例1〜5に示す通り、本発明の製造方法に用いられ
る接着剤はエマルジョンであり火災等の危険性が々く、
可使時間も長く作業性がよく、自動車の内装材としての
接着性、特に耐熱、耐水性に優れていることが判る。尚
、実施例5よりエポキシ樹脂を添加しない試料(は、耐
熱性9耐水性が劣り、又エポキシ樹脂が2%以下の場合
は接着性が悪く々す、35%以上の場合は可使時間が短
かくなることがわかる。
Table 4: True 1 Lie: Adhesive strength after being left at room temperature for 24 hours after lamination *6 Heat resistance: 3 at 80°C after being left at room temperature for 24 hours after lamination
Adhesive strength after being left for a while *7 Heat aging resistance: 80°C after being left at room temperature for 24 hours after lamination
Adhesive strength after being left for 20 days at room temperature, water resistance: Adhesive strength after being left at room temperature for 24 hours after lamination, and then immersed in water at 20°C for 24 hours As shown in Examples 1 to 5, the manufacturing method of the present invention The adhesive used is an emulsion and has a high risk of fire.
It has a long pot life, good workability, and is found to have excellent adhesive properties as an interior material for automobiles, especially in heat resistance and water resistance. In addition, from Example 5, samples without epoxy resin (heat resistance 9) are inferior in water resistance, and when the epoxy resin content is less than 2%, the adhesion is poor, and when the epoxy resin content is 35% or more, the pot life is shortened. You can see that it will be shorter.

Claims (1)

【特許請求の範囲】[Claims] エマルジョン型接着剤と、エポキシ樹脂との混合物を主
体とした接着剤を用いて基材と表装材とを貼合わせるこ
とを特徴とする自動車内装材の製造方法
A method for producing an automobile interior material, which comprises laminating a base material and a facing material using an adhesive mainly consisting of a mixture of an emulsion type adhesive and an epoxy resin.
JP61268170A 1986-11-11 1986-11-11 Production of automotive interior material Pending JPS63126981A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61268170A JPS63126981A (en) 1986-11-11 1986-11-11 Production of automotive interior material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61268170A JPS63126981A (en) 1986-11-11 1986-11-11 Production of automotive interior material

Publications (1)

Publication Number Publication Date
JPS63126981A true JPS63126981A (en) 1988-05-30

Family

ID=17454883

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61268170A Pending JPS63126981A (en) 1986-11-11 1986-11-11 Production of automotive interior material

Country Status (1)

Country Link
JP (1) JPS63126981A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20180005235A (en) * 2015-05-12 2018-01-15 한화 아즈델 인코포레이티드 Lower shielding composition and article providing improved peel strength and methods of use thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5113227A (en) * 1974-07-24 1976-02-02 Canon Kk MUKOROORUFUIRUMUSHONO DENDOSHIKI FUIRUMUOKURIKAMERANO SADOSOCHI
JPS60181181A (en) * 1984-02-29 1985-09-14 Aica Kogyo Co Ltd Aqueous dispersed two-pack type adhesive
JPS6153378A (en) * 1984-08-21 1986-03-17 Sunstar Giken Kk Two-pack type adhesive

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5113227A (en) * 1974-07-24 1976-02-02 Canon Kk MUKOROORUFUIRUMUSHONO DENDOSHIKI FUIRUMUOKURIKAMERANO SADOSOCHI
JPS60181181A (en) * 1984-02-29 1985-09-14 Aica Kogyo Co Ltd Aqueous dispersed two-pack type adhesive
JPS6153378A (en) * 1984-08-21 1986-03-17 Sunstar Giken Kk Two-pack type adhesive

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20180005235A (en) * 2015-05-12 2018-01-15 한화 아즈델 인코포레이티드 Lower shielding composition and article providing improved peel strength and methods of use thereof
JP2018522755A (en) * 2015-05-12 2018-08-16 ハンファ アズデル インコーポレイテッド Underbody shield composition, articles with improved peel strength, and methods of use thereof
US10981606B2 (en) 2015-05-12 2021-04-20 Hanwha Azdel, Inc. Underbody shield compositions and articles that provide enhanced peel strength
JP2022116035A (en) * 2015-05-12 2022-08-09 ハンファ アズデル インコーポレイテッド UNDERBODY SHIELD COMPOSITIONS AND ARTICLES WITH IMPROVED PEEL STRENGTH AND METHODS OF USE THEREOF

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