JPH08302315A - Aqueous two-part adhesive for vacuum molding of polyolefin foamed sheet - Google Patents
Aqueous two-part adhesive for vacuum molding of polyolefin foamed sheetInfo
- Publication number
- JPH08302315A JPH08302315A JP14797795A JP14797795A JPH08302315A JP H08302315 A JPH08302315 A JP H08302315A JP 14797795 A JP14797795 A JP 14797795A JP 14797795 A JP14797795 A JP 14797795A JP H08302315 A JPH08302315 A JP H08302315A
- Authority
- JP
- Japan
- Prior art keywords
- pts
- carboxyl
- parts
- chloroprene rubber
- curing agent
- 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
Links
- 239000000853 adhesive Substances 0.000 title claims abstract description 19
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 19
- 229920000098 polyolefin Polymers 0.000 title claims abstract description 8
- 238000000465 moulding Methods 0.000 title abstract 2
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 25
- 229920001084 poly(chloroprene) Polymers 0.000 claims abstract description 14
- 239000000839 emulsion Substances 0.000 claims abstract description 12
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical class ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920000126 latex Polymers 0.000 claims abstract description 11
- 239000004816 latex Substances 0.000 claims abstract description 10
- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 claims abstract description 9
- 239000007787 solid Substances 0.000 claims abstract description 9
- 239000006260 foam Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 238000007666 vacuum forming Methods 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 229920005989 resin Polymers 0.000 abstract description 11
- 239000011347 resin Substances 0.000 abstract description 11
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 abstract description 7
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 abstract description 7
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 abstract description 7
- 239000000178 monomer Substances 0.000 description 6
- -1 for example Chemical compound 0.000 description 5
- 229920001568 phenolic resin Polymers 0.000 description 4
- 239000005011 phenolic resin Substances 0.000 description 4
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical class CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- BQBSIHIZDSHADD-UHFFFAOYSA-N 2-ethenyl-4,5-dihydro-1,3-oxazole Chemical compound C=CC1=NCCO1 BQBSIHIZDSHADD-UHFFFAOYSA-N 0.000 description 1
- PBYIFPWEHGSUEY-UHFFFAOYSA-N 2-ethenyl-4-methyl-4,5-dihydro-1,3-oxazole Chemical compound CC1COC(C=C)=N1 PBYIFPWEHGSUEY-UHFFFAOYSA-N 0.000 description 1
- LPIQIQPLUVLISR-UHFFFAOYSA-N 2-prop-1-en-2-yl-4,5-dihydro-1,3-oxazole Chemical compound CC(=C)C1=NCCO1 LPIQIQPLUVLISR-UHFFFAOYSA-N 0.000 description 1
- MBLQIMSKMPEILU-UHFFFAOYSA-N 4-methyl-2-prop-1-en-2-yl-4,5-dihydro-1,3-oxazole Chemical compound CC1COC(C(C)=C)=N1 MBLQIMSKMPEILU-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、水性2液形接着剤、更
に詳しくはカルボキシル変性クロロプレンゴムラテック
ス、粘着付与剤の混合水性エマルジョン主剤と、オキサ
ゾリン基含有エマルジョン形硬化剤からなり、真空成形
接着可能なポリオレフィン系発泡シートへの密着性、お
よび硬化後の耐熱性に優れ、可使時間(ここで言う可使
時間とは、接着剤を塗付、乾燥後から貼合せを行うまで
の時間をさす)、ポットライフが長い、水性2液形接着
剤に関する。FIELD OF THE INVENTION The present invention relates to a water-based two-component adhesive, more specifically, a carboxyl-modified chloroprene rubber latex, a mixed water-based emulsion main agent of a tackifier, and an oxazoline group-containing emulsion type curing agent. It has excellent adhesiveness to a polyolefin foam sheet and heat resistance after curing, and has a usable time (the usable time here is the time from applying and drying the adhesive to laminating. As expected, the present invention relates to an aqueous two-component adhesive having a long pot life.
【0002】[0002]
【従来の技術と発明が解決しようとする課題】従来よ
り、一般に用いられている水性2液形接着剤はポリウレ
タンエマルジョンを主成分とし、粘着付与剤を混合した
水性エマルジョン主剤と水分散性イソシアネートを硬化
剤とする水性2液形接着剤であり、ポリオレフィン系発
泡シートへの初期密着が困難であり、又可使時間、ポッ
トライフが短いという欠点があった。さらに、カルボキ
シル変性クロロプレンゴムラテックスと粘着付与剤の混
合水性エマルジョン主剤と水分散性イソシアネートを硬
化剤とする水性2液形接着剤では所望の耐熱性を得るた
めに必要な量の硬化剤を配合すると初期密着性が低下し
てしまう問題があった。従って、ポリオレフィン系発泡
シートの真空成形接着には初期密着性、硬化後の耐熱
性、可使時間、ポットライフが求められ、全ての特徴を
満たす水性接着剤が望まれていた。2. Description of the Related Art Conventionally, water-based two-component type adhesives generally used have a polyurethane emulsion as a main component and a water-dispersible isocyanate and an aqueous emulsion main component mixed with a tackifier. It is an aqueous two-component adhesive as a curing agent, and has the drawbacks that initial adhesion to a polyolefin foam sheet is difficult and that the pot life and pot life are short. Furthermore, in an aqueous two-component adhesive containing a carboxyl-modified chloroprene rubber latex and a tackifier as a mixed aqueous emulsion main agent and a water-dispersible isocyanate as a curing agent, a curing agent in an amount necessary for obtaining desired heat resistance is added. There was a problem that the initial adhesion was lowered. Therefore, initial adhesion, heat resistance after curing, pot life, and pot life are required for vacuum forming adhesion of a polyolefin foam sheet, and a water-based adhesive satisfying all the characteristics has been desired.
【0003】[0003]
【課題を解決するための手段】そこで、本発明は上記カ
ルボキシル変性クロロプレンゴムラテックスの水性接着
剤の初期密着性及び硬化後の耐熱性を可使時間、ポット
ライフを損なわずにポリオレフィン系発泡体の真空成形
接着可能な溶剤形接着剤と同等もしくはそれ以上に接着
性が発現されるべく鋭意検討を進めたところ硬化剤とし
てオキサゾリン基含有エマルジョンを用いることにより
初期目的の水性2液形接着剤が得られることを見いだす
に至った。Accordingly, the present invention provides the above-mentioned carboxyl-modified chloroprene rubber latex with a water-based adhesive having an initial adhesiveness and a heat resistance after curing, which is a polyolefin-based foam without impairing pot life and pot life. As a result of intensive studies to develop adhesiveness equivalent to or more than solvent-type adhesives capable of vacuum forming adhesion, the use of an oxazoline group-containing emulsion as a curing agent yields an aqueous two-component adhesive for the initial purpose. I came to find out that it is possible to be.
【0004】この発明における、カルボキシル変性クロ
ロプレンゴムラテックスは、クロロプレンゴム分子中に
少なくとも1つ以上のカルボキシル基を有するクロロプ
レンゴムでありクロロプレン単量体をこれと共重合し得
る不飽和脂肪族有機カルボン酸、例えばアクリル酸、メ
タクリル酸、イタコン酸等とを乳化重合法で共重合する
ことにより得られる。The carboxyl-modified chloroprene rubber latex in the present invention is a chloroprene rubber having at least one carboxyl group in the chloroprene rubber molecule and is an unsaturated aliphatic organic carboxylic acid capable of copolymerizing a chloroprene monomer with the chloroprene rubber. , For example, acrylic acid, methacrylic acid, itaconic acid and the like by copolymerization by an emulsion polymerization method.
【0005】粘着付与剤としては、水添ロジン、重合ロ
ジン、マレイン酸変性ロジン、水添ロジンエステル等
の、ロジン系樹脂、アルキルフェノール樹脂、ロジン変
性フェノール樹脂、テルペン変性フェノール樹脂等のフ
ェノール系樹脂、天然及び合成テルペン樹脂、クマロン
−インデン樹脂、クマロン−インデン−スチレン樹脂、
脂肪族系及び芳香族石油樹脂等が用いることができ、特
に、ロジン系樹脂、フェノール系樹脂、テルペン樹脂が
好ましい。Examples of tackifiers include hydrogenated rosin, polymerized rosin, maleic acid-modified rosin, hydrogenated rosin ester, and other rosin-based resins, alkylphenol resins, rosin-modified phenolic resins, terpene-modified phenolic resins, and other phenolic resins. Natural and synthetic terpene resin, coumarone-indene resin, coumarone-indene-styrene resin,
Aliphatic and aromatic petroleum resins can be used, and rosin resins, phenolic resins, and terpene resins are particularly preferable.
【0006】粘着付与樹脂の使用量(固形分換算)は通
常、上記カルボキシル変性クロロプレンゴムラテックス
100部重量部に対して5〜100部の範囲で設定すれ
ばよい。5部未満及び100部を越えると、所望の初期
密着性が得られず、また硬化後の耐熱性が低下する傾向
となる。The amount of the tackifying resin used (in terms of solid content) may usually be set in the range of 5 to 100 parts by weight per 100 parts by weight of the carboxyl-modified chloroprene rubber latex. If it is less than 5 parts or more than 100 parts, the desired initial adhesion cannot be obtained, and the heat resistance after curing tends to decrease.
【0007】本発明に用いられるオキサゾリン基を含有
する架橋剤には以下のオキサゾリン基を持つ単量体を用
いることができる。例えば、2−ビニル−2−オキサゾ
リン、2−ビニル−4−メチル−オキサゾリン、2−イ
ソプロペニル−2−オキサゾリン、2−イソプロペニル
−4−メチル−2−オキサゾリン、2−イソプロペニル
−5−エチル−2−オキサゾリン等で、これらの中から
1種類または、2種類以上を選択し使用することができ
る。また、これらのオキサゾリン基を持つ単量体は次に
示すようなビニル単量体成分を共重合成分として用いる
ことができる。ビニル単量体成分はオキサゾリンと共重
合し、オキサゾリンと相互作用を起こさないものであれ
ば特に制限はなく、例えば、アクリル酸メチル、アクリ
ル酸ブチル、アクリル酸2−エチルヘキシル等のアクリ
ル酸エステル類、アクリル酸ニトリル等の不飽和ニトリ
ル類、酢酸ビニル、プロピオン酸ビニル等のビニルエス
テル類、メチルビニルエーテル、エチルビニルエーテル
等のビニルエーテル類、エチレン、プロピレン等のα−
オレフィン類、塩化ビニル、塩化ビニリデン、フッ化ビ
ニル等のα,β−不飽和芳香族モノマー等があげられ、
これらの1種類または2種類以上を使用することが出来
る。The following monomers having an oxazoline group can be used for the crosslinking agent containing an oxazoline group used in the present invention. For example, 2-vinyl-2-oxazoline, 2-vinyl-4-methyl-oxazoline, 2-isopropenyl-2-oxazoline, 2-isopropenyl-4-methyl-2-oxazoline, 2-isopropenyl-5-ethyl. 2-oxazoline and the like can be used alone or in combination of two or more. Further, as the monomers having these oxazoline groups, the following vinyl monomer components can be used as a copolymerization component. The vinyl monomer component is not particularly limited as long as it is copolymerized with oxazoline and does not interact with oxazoline, for example, methyl acrylate, butyl acrylate, acrylic acid esters such as 2-ethylhexyl acrylate, Unsaturated nitriles such as acrylic acid nitrile, vinyl acetates such as vinyl acetate and vinyl propionate, vinyl ethers such as methyl vinyl ether and ethyl vinyl ether, α-such as ethylene and propylene.
Examples include α, β-unsaturated aromatic monomers such as olefins, vinyl chloride, vinylidene chloride and vinyl fluoride,
These 1 type or 2 types or more can be used.
【0008】本発明に係る水性2液形接着剤は、上記所
定割合のカルボキシル変性クロロプレンゴムラテックス
および粘着付与樹脂からなる主剤と、オキサゾリン基含
有エマルジョン形硬化剤との2液形で構成され、接着使
用の直前に主剤と硬化剤を計量混合する。必要に応じ
て、主剤に通常の増粘剤を加えて、主剤粘度を通常10
00〜10000cps/20℃に調整してもよい。硬
化剤の使用量は通常、主剤量100重量部(固形分換
算)に対して3〜30重量部の範囲で設定すればよい。
3重量部未満および30重量部を越えると、十分な硬化
後の耐熱性が得られず、接着性が低下する傾向となる。The aqueous two-pack type adhesive agent according to the present invention comprises a two-pack type of a main agent consisting of the carboxyl-modified chloroprene rubber latex and the tackifying resin in the above-mentioned predetermined proportions, and an oxazoline group-containing emulsion type hardening agent. Just before use, measure and mix the base compound and the curing agent. If necessary, an ordinary thickener is added to the main agent so that the viscosity of the main agent is usually 10
You may adjust to 00-10,000 cps / 20 degreeC. The amount of the curing agent used is usually set in the range of 3 to 30 parts by weight with respect to 100 parts by weight of the main agent (solid content conversion).
If it is less than 3 parts by weight or more than 30 parts by weight, sufficient heat resistance after curing cannot be obtained, and the adhesiveness tends to decrease.
【0009】[0009]
【発明の効果】以上の構成からなる本発明接着剤は、良
好な初期接着特性および硬化後の耐熱性を発揮し、可使
時間、ポットライフが長くかつ、ポリオレフィン系発泡
シートの真空成形接着が可能である。EFFECT OF THE INVENTION The adhesive of the present invention having the above constitution exhibits good initial adhesive properties and heat resistance after curing, has a long pot life and a long pot life, and is capable of vacuum forming and adhering a polyolefin foam sheet. It is possible.
【0010】[0010]
【実施例】次に、実施例によって本発明をさらに詳細に
説明するが、本発明はこれらの例によって限定されるも
のではない。 実施例1および比較例1〜3 (1)主剤 下記表1に示す部数のカルボキシル変性クロロプレンゴ
ムラテックス、またはウレタンエマルジョン、および粘
着付与剤、増粘剤を配合して、主剤を得た。 (2)架橋剤 上記(1)の主剤100部に対し、硬化剤としてオキサ
ゾリン基含有エマルジョン(日本触媒製、CX−WS−
120)5部、またはポリメリックMDI(日本ポリウ
レタン社製、コロネート3053)5部混合して接着剤
とした。EXAMPLES Next, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples. Examples 1 and Comparative Examples 1 to 3 (1) Main Agent A carboxyl-modified chloroprene rubber latex or urethane emulsion in the number of parts shown in Table 1 below, and a tackifier and a thickener were blended to obtain a main agent. (2) Crosslinking agent An oxazoline group-containing emulsion (manufactured by Nippon Shokubai Co., Ltd., CX-WS-
120) 5 parts or Polymeric MDI (manufactured by Nippon Polyurethane Company, Coronate 3053) 5 parts were mixed to prepare an adhesive.
【0011】(3)接着試験 上記(2)の接着剤をよく攪拌混合してから2時間常温
に放置した後、木質ボードに150g/m2の量で塗付
し、80℃で5分間乾燥した後、オープンタイム30分
とり、これに予め140℃に加熱した発泡ポリプロピレ
ンシートを0.5kg/cm2の圧力で15秒間圧着し
て、試験片を作成した。ついで、下記試験項目に供し、
結果を表1に併記する。(3) Adhesion test After the adhesive of the above (2) was thoroughly stirred and mixed and left at room temperature for 2 hours, it was applied on a wooden board at an amount of 150 g / m 2 and dried at 80 ° C. for 5 minutes. After that, the open time was taken for 30 minutes, and a foamed polypropylene sheet preheated to 140 ° C. was pressure-bonded thereto at a pressure of 0.5 kg / cm 2 for 15 seconds to prepare a test piece. Then, provide the following test items,
The results are also shown in Table 1.
【0012】初期剥離強度 貼合せ直後、引張速度200mm/分、25mm巾、1
80度剥離強度(kg/25mm)を測定した。初期耐熱クリープ 貼合せ直後、80℃雰囲気中、100g/25mmの荷
重を90度で加え、1時間後の剥離長さ(mm)を測定
した。常態耐熱クリープ 貼合せ後20℃、65%RHで24時間養生した後、8
0℃雰囲気中、100g/25mmの荷重を90度で加
え、24時間後の剥離長さ(mm)を測定した。 Initial peel strength Immediately after laminating, tensile speed is 200 mm / min, 25 mm width, 1
The 80 degree peel strength (kg / 25 mm) was measured. Immediately after the initial heat-resistant creep bonding, a load of 100 g / 25 mm was applied at 90 degrees in an atmosphere of 80 ° C., and the peel length (mm) after 1 hour was measured. 8 hours after curing at 20 ℃ and 65% RH for 24 hours after laminating normal heat resistant creep
In a 0 ° C. atmosphere, a load of 100 g / 25 mm was applied at 90 degrees, and the peeling length (mm) after 24 hours was measured.
【0013】[0013]
【表1】 注1)電気化学社製、LC−501、固形分47% 注2)バイエル社製、Dispercoll KA−8
464、固形分40% 注3)吉村油化学製、ユカレジンKE−904、固形分
55% 注4)ヘキスト製,Borchigel L−75 注5)Aは発泡ポリプロピレンシート界面剥離、Bは材
料破壊[Table 1] Note 1) Electrochemical Co., LC-501, solid content 47% Note 2) Bayer Co., Dispercoll KA-8
464, solid content 40% Note 3) Yoshimura Yushi Kagaku, Yucarezin KE-904, solid content 55% Note 4) Hoechst, Borchigel L-75 Note 5) A is a polypropylene polypropylene sheet interface peeling, B is material destruction
Claims (2)
クスと粘着付与剤を必須成分として含む主剤と、オキサ
ゾリン基含有エマルジョン形硬化剤からなり、ポリオレ
フィン系発泡シートの真空成形接着が可能であることを
特徴とする水性2液形接着剤。1. A water-based composition comprising a base compound containing a carboxyl-modified chloroprene rubber latex and a tackifier as essential components, and an oxazoline group-containing emulsion type curing agent, which enables vacuum forming adhesion of a polyolefin foam sheet. Two-component adhesive.
算)が、カルボキシル変成クロロプレンゴムラテックス
の固形分100重量部に対し5〜100重量部でかつ硬
化剤の使用量が主剤100重量部に対し3〜30重量部
である請求項1記載の水性2液形接着剤。2. The amount of the tackifying emulsion (in terms of solid content) is 5 to 100 parts by weight based on 100 parts by weight of the solid content of the carboxyl-modified chloroprene rubber latex, and the amount of the curing agent used is based on 100 parts by weight of the main agent. The aqueous two-component adhesive according to claim 1, which is 3 to 30 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14797795A JPH08302315A (en) | 1995-05-12 | 1995-05-12 | Aqueous two-part adhesive for vacuum molding of polyolefin foamed sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14797795A JPH08302315A (en) | 1995-05-12 | 1995-05-12 | Aqueous two-part adhesive for vacuum molding of polyolefin foamed sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH08302315A true JPH08302315A (en) | 1996-11-19 |
Family
ID=15442386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14797795A Pending JPH08302315A (en) | 1995-05-12 | 1995-05-12 | Aqueous two-part adhesive for vacuum molding of polyolefin foamed sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH08302315A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6180244B1 (en) | 1998-02-17 | 2001-01-30 | 3M Innovative Properties Company | Waterbased thermoforming adhesives |
JP2001262041A (en) * | 2000-03-16 | 2001-09-26 | Hitachi Kasei Polymer Co Ltd | Aqueous primer composition |
US6306942B1 (en) | 2000-04-05 | 2001-10-23 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesives |
US6310125B1 (en) | 2000-04-05 | 2001-10-30 | 3M Innovative Properties Company | Water-dispersed adhesive compositions |
US6541550B1 (en) | 2000-04-05 | 2003-04-01 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesive compositions |
-
1995
- 1995-05-12 JP JP14797795A patent/JPH08302315A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6180244B1 (en) | 1998-02-17 | 2001-01-30 | 3M Innovative Properties Company | Waterbased thermoforming adhesives |
JP2001262041A (en) * | 2000-03-16 | 2001-09-26 | Hitachi Kasei Polymer Co Ltd | Aqueous primer composition |
JP4596599B2 (en) * | 2000-03-16 | 2010-12-08 | 日立化成ポリマー株式会社 | Water-based primer composition |
US6306942B1 (en) | 2000-04-05 | 2001-10-23 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesives |
US6310125B1 (en) | 2000-04-05 | 2001-10-30 | 3M Innovative Properties Company | Water-dispersed adhesive compositions |
US6541550B1 (en) | 2000-04-05 | 2003-04-01 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesive compositions |
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