JPS60203683A - Adhesive - Google Patents

Adhesive

Info

Publication number
JPS60203683A
JPS60203683A JP3112984A JP3112984A JPS60203683A JP S60203683 A JPS60203683 A JP S60203683A JP 3112984 A JP3112984 A JP 3112984A JP 3112984 A JP3112984 A JP 3112984A JP S60203683 A JPS60203683 A JP S60203683A
Authority
JP
Japan
Prior art keywords
emulsion
ethylene
adhesive
vinyl
vinyl ester
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.)
Granted
Application number
JP3112984A
Other languages
Japanese (ja)
Other versions
JPH0613684B2 (en
Inventor
Shizuo Narisawa
成沢 静夫
Hiroyuki Shiono
塩野 裕幸
Choji Tomizawa
長二 富沢
Yasuo Kanejima
金島 保夫
Masahiro Domoto
道本 雅宏
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP59031129A priority Critical patent/JPH0613684B2/en
Publication of JPS60203683A publication Critical patent/JPS60203683A/en
Publication of JPH0613684B2 publication Critical patent/JPH0613684B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:A one-pack adhesive suitable for bonding polyolefin, etc., having improved water-resistant and heat-resistant bond strength, comprising an ethylene- vinyl ester multi-copolymer emulsion and a polyurethane emulsion. CONSTITUTION:(A) An ethylene-vinyl ester multi-copolymer emulsion obtained by subjecting (i) 5-35wt% ethylene, (ii) 2-50wt% vinyl acetate, and (iii) 35-90wt% total amount of a higher carboxylic acid vinyl ester (preferably vinyl pivalate, etc.) and an acrylic ester (e.g., butyl acrylate, etc.) (with the proviso that a weight ratio of the former to the latter of 100:0-60:40) to emulsion polymerization preferably by the use of PVA as an emulsion dispersant is blended with (B) a polyurethane emulsion (preferably anionic emulsion), to give the desired adhesive. A ratio of solid content of the component A:B is usually 95:5-60:40.

Description

【発明の詳細な説明】 本発明は水性コンタクト接着剤に関するものであり、さ
らに詳しくは、特定の共重合組成を有スルエチレンービ
ニルエステル系多元共重合体エマルジョンとポリウレタ
ンエマルジョンとを含有することを特徴とする耐水およ
び耐熱接着力に優れ、しかもポリオレフィン系被着材に
対しても優れた接着力を示す1液型の水性コンタクト接
着剤に関するものである。被着体に接着剤を塗布し乾燥
せしめた状態で貼合せ、圧着して接着せしめるタイプの
コンタクト接着剤がゴム、金属、プラスチックなどの同
種または異種祠料間の接着に使用されている。かかるコ
ンタクト接着剤としては従来より有機溶剤型のクロロプ
レン系のものが使用されていたが、安全衛生、大気汚染
および火災危険などの理由からより安全な水性型のコン
タクト接着剤が要求されている。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an aqueous contact adhesive, and more particularly, an aqueous contact adhesive containing a sulfethylene-vinyl ester multi-component copolymer emulsion having a specific copolymer composition and a polyurethane emulsion. The present invention relates to a one-component water-based contact adhesive that has characteristics of excellent water resistance and heat resistant adhesive strength, and also exhibits excellent adhesive strength to polyolefin adherends. Contact adhesives are used to bond similar or different types of abrasive materials, such as rubber, metal, and plastic, by applying an adhesive to an adherend, letting it dry, then bonding and pressing. Conventionally, organic solvent-based chloroprene-based contact adhesives have been used, but safer water-based contact adhesives are required for reasons such as health and safety, air pollution, and fire hazards.

かかる要求に対してアクリル酸エステル系エマルジョン
が水性コンタクト接着剤として一部上市されてはいるが
耐水接着力の点で満足できるものでな(、さらに近年使
用分野が拡大している輩ゴム、ポリエチレンフオームな
ど、一般に接着性に劣ると言われているポリオレフィン
系被着材に対してはコンタクト性そのものが不充分であ
った。一方、ポリオレフィン系被着材に対する単なる感
圧接着剤として、エチレン−酢酸ビニル−高級カルボン
酸ビニルエステル系共重合体エマルジョンおよびエチレ
ン−酢酸ビニル−高級カルボン酸ビニルエステル−アク
リル酸エステル系共重合体エマルジョンが提案されてい
る(特公昭51−12653 号公報、特開昭52−4
7833号公報、特開昭53−73235号公報)が、
コンタクト接着剤として使用する場合は耐熱および耐水
接着力が充分満足されるものではなかった。また耐熱お
よび耐水接着力の改善を目的とした水性コンタクト接着
剤としてエチレン−ビニルエステル系共重合体エマルジ
ョンにイソシアネート化合物を添加した組成物も提案さ
れてはいるが、接着剤が2液の形態を取るため使用直前
に混合する必要があるなど作業性の面で好ましいもので
はなかった。
In response to these demands, some acrylic acid ester emulsions have been put on the market as water-based contact adhesives, but they are not satisfactory in terms of water-resistant adhesion (in addition, rubber and polyethylene emulsions, whose use has expanded in recent years) The contact property itself was insufficient for polyolefin-based adherends, such as foam, which are generally said to have poor adhesive properties.On the other hand, ethylene-acetic acid was used as a simple pressure-sensitive adhesive for polyolefin-based adherends. Vinyl-higher carboxylic acid vinyl ester copolymer emulsions and ethylene-vinyl acetate-higher carboxylic acid vinyl ester-acrylic acid ester copolymer emulsions have been proposed (Japanese Patent Publication No. 12653/1983, JP-A-52 -4
No. 7833, Japanese Unexamined Patent Publication No. 73235/1983),
When used as a contact adhesive, heat resistance and water resistance adhesive strength were not fully satisfied. In addition, a composition in which an isocyanate compound is added to an ethylene-vinyl ester copolymer emulsion has been proposed as a water-based contact adhesive for the purpose of improving heat-resistant and water-resistant adhesive strength, but the adhesive is in a two-component form. This was not desirable in terms of workability, as it required mixing immediately before use.

本発明者らは、かかるコンタクト接着剤の問題点を解決
すべく、鋭意検討を行った結果、特定のエチレン−ビニ
ルエステル系多元共重合体エマルシコンとポリウレタン
エマルジッンとを含有することを特徴とする水性接着剤
が、ポリオレフィン系以外の被着材はもとよりポリオレ
フィン系被着材についてもコンタクト性のみならず耐水
および耐熱接着力に優れ、しかも作業性に優れた1液型
の形態を取り得ることを見出し本発明を完成した。
In order to solve the problems of such contact adhesives, the present inventors conducted intensive studies and found that the contact adhesive is characterized by containing a specific ethylene-vinyl ester multi-component copolymer emulsicon and a polyurethane emulsion. The water-based adhesive has excellent contact properties as well as water and heat resistant adhesion for non-polyolefin adherends as well as polyolefin adherends, and can take the form of a one-component type with excellent workability. They found this and completed the present invention.

すなわち、本発明はエチレン5〜35wt%、酢酸ビニ
ル2〜5賞、高級カルボン酸ビニルエステルとアクリル
酸エステルの合計量3も〜9字〜を含有し、高級カルボ
ン酸ビニルエステルとアクリル酸エステルの重量比が1
00 : 0〜60:40である共重合体組成のエチレ
ン−ビニルエステル系多元共重合体エマルジョンとポリ
ウレタンエマルジ目ンとを含有することを特徴とする水
性コンタクト接着剤を提供するものである。
That is, the present invention contains 5 to 35 wt% of ethylene, 2 to 5 percent of vinyl acetate, the total amount of higher carboxylic acid vinyl ester and acrylic ester is 3 to 9 characters, and the total amount of higher carboxylic acid vinyl ester and acrylic ester is Weight ratio is 1
The present invention provides an aqueous contact adhesive characterized by containing an ethylene-vinyl ester multicomponent copolymer emulsion having a copolymer composition of 0:0 to 60:40 and a polyurethane emulsion.

本発明に使用される該エチレン−ビニルエステル系多元
共重合体エマルジョンの共重合体中のエチレン含量は5
〜35 we %であり、5wt%以下ではポリオレフ
ィン被着体のコンタク性に劣り、35Wt’S以上では
耐熱性に劣る。また共重合体中の酢酸ビニル含量は2〜
sowtsであり、2wt%以下では共重合体エマルジ
ョンの安定性に劣り、50wt%以上ではコンタクト性
に劣る。
The ethylene content in the copolymer of the ethylene-vinyl ester multi-component copolymer emulsion used in the present invention is 5
-35 Wt'S, and if it is less than 5 wt%, the contact properties of the polyolefin adherend will be poor, and if it is more than 35 Wt'S, it will be poor in heat resistance. In addition, the vinyl acetate content in the copolymer is 2-
If the amount is less than 2 wt%, the stability of the copolymer emulsion is poor, and if it is more than 50 wt%, the contact property is poor.

本発明に使用される共重合体エマルジョン中の共重合体
は、高級カルボン酸ビニルニスデルとアクリル酸エステ
ルの合計含量が35〜QQwtチであり、その重量比が
100 : 0〜60:40である。合計含量がasw
ts以下ではコンタクト性に劣り、9Qwt%以上では
、ポリウレタンを混合した場合のエマルジョンの安定性
が劣る。
The copolymer in the copolymer emulsion used in the present invention has a total content of vinyl higher carboxylic acid Nisder and acrylic ester of 35 to QQwt, and a weight ratio of 100:0 to 60:40. The total content is asw
If it is less than ts, the contact properties will be poor, and if it is more than 9 Qwt%, the stability of the emulsion when mixed with polyurethane will be poor.

また、高級カルボン酸ビニルエステルとアクリル酸エス
テルの比率が上記範囲をはずれるとコンタクト性が劣る
傾向があり好ましくない。
Furthermore, if the ratio of higher carboxylic acid vinyl ester and acrylic ester is out of the above range, contact properties tend to be poor, which is not preferable.

本発明で用いられる高級カルボン酸ビニルエステルとし
てはピバリン酸ビニル、ラウリン酸ビニル、パーサティ
ック酸ビニル(Veo*a−10ニジ工ル化学社製)な
どの炭素数5〜12の高級カルボン酸が好ましく使用さ
れる。また本発明に用いられるアクリル酸エステルとし
ては、アクリル酸ブチル、アクリル酸ペンチル、アクリ
ル酸オクチル、アクリル酸2エチルヘキシルなどの炭素
数4以上のアルコールから誘導されるアクリル酸エステ
ルがあげられる。
The higher carboxylic acid vinyl ester used in the present invention is preferably a higher carboxylic acid having 5 to 12 carbon atoms, such as vinyl pivalate, vinyl laurate, or vinyl persate (Veo*a-10 manufactured by Niji Engineering Chemical Co., Ltd.). used. Examples of the acrylic ester used in the present invention include acrylic esters derived from alcohols having 4 or more carbon atoms, such as butyl acrylate, pentyl acrylate, octyl acrylate, and 2-ethylhexyl acrylate.

本発明の多元系共重合体は上記単量体を上記量の範囲で
含有するものであれば上記単量体の他に、プロピオン酸
ビニル、酪酸ビニル等のビニルエステル、マレイン酸ジ
エステル、フマール酸ジエステルなどを共重合したもの
でも良く、さらに水酸基、アミド基、カルボキシル基、
スルフォン酸基、エポキシ基、アルコキシ基、メチロー
ル基などの官能基含有モノマーをlQwtチ以下含有し
たものであっても良い。
The multicomponent copolymer of the present invention contains the above-mentioned monomers in the above-mentioned amounts, in addition to the above-mentioned monomers, vinyl esters such as vinyl propionate and vinyl butyrate, diester maleate, and fumaric acid. Copolymerization of diester etc. may also be used, and furthermore, hydroxyl group, amide group, carboxyl group, etc.
It may contain a monomer containing a functional group such as a sulfonic acid group, an epoxy group, an alkoxy group, or a methylol group in an amount of 1Qwt or less.

本発明で使用されるエチレン−ビニルエステル系多元共
重合体エマルジョンは通常の乳化重合法によって製造さ
れるが、この際に使用される乳化分散剤は、接着剤とし
た場合の塗布適性からポリビニルアルコールが好ましい
。ポリビニルアルコールとしては一般に乳化分散剤とし
て用いられる平均ケン化度70〜99.5モルチ、平均
重合度200〜2700のもの、または、該ポリビニル
アルコールをカルボン酸、スルフォン酸あるいはグリオ
キザールなどで変性したものが使用でき、さらにヒドロ
キシエチルセルロース系の保護コロイド、ノニオンおよ
びアニオン乳化剤を併用しても良い。
The ethylene-vinyl ester multi-component copolymer emulsion used in the present invention is produced by a normal emulsion polymerization method, and the emulsifying dispersant used at this time is polyvinyl alcohol because of its suitability for application when used as an adhesive. is preferred. As polyvinyl alcohol, those having an average saponification degree of 70 to 99.5 mol and an average polymerization degree of 200 to 2,700, which are generally used as emulsifying dispersants, or those modified with carboxylic acid, sulfonic acid, glyoxal, etc. are used as polyvinyl alcohol. In addition, hydroxyethylcellulose-based protective colloids, nonionic and anionic emulsifiers may be used in combination.

本発明は、かかるエチレン−ビニルエステル系多元共重
合体エマルジョンとポリウレタンエマルジョンとを含有
することを′特徴とする接着剤であるが、その固形分含
有割合は通常95:5〜60:40の範囲である。ポリ
ウレタンエマルジョンとしてはウレタン樹脂の主鎖また
は側鎖に新水基を導入して乳化せしめたものであり、ス
ルフォン酸塩またはカルボン酸塩などを導入したアニオ
ン性ポリウレタンエマルジョンカエチレンービニルエス
テル系多元共重合体エマルジョンとの安定性から好まし
く使用される。
The present invention is an adhesive characterized by containing such an ethylene-vinyl ester multi-component copolymer emulsion and a polyurethane emulsion, the solid content ratio of which is usually in the range of 95:5 to 60:40. It is. Polyurethane emulsions are emulsified by introducing new water groups into the main chain or side chains of urethane resins, and are anionic polyurethane emulsions containing sulfonates or carboxylates, ethylene-vinyl ester-based polyesters, etc. It is preferably used because of its stability with polymer emulsions.

本発明はかかるエマルジョンに必要に応じ一般の水性接
着剤に使用されている添加剤、たとえば、増粘剤、溶剤
、粘着付与剤、顔料などを配合することもできる。
In the present invention, additives used in general water-based adhesives, such as thickeners, solvents, tackifiers, pigments, etc., may be added to the emulsion as necessary.

かくして得られた本発明の接着剤はコンタクト性のみな
らず、耐水および耐熱、接着力に優れ、しかも作業性に
優れた1液型の接着剤であるため中ゴム、ポリエチレン
フオームなどのポリオレフィンをはじめ布、紙、木材、
モルタル金属などの同種または異種材料間の接着に使用
できる。
The thus obtained adhesive of the present invention has excellent not only contact properties but also water resistance, heat resistance, and adhesive strength, and is a one-component adhesive with excellent workability, so it can be used with polyolefins such as medium rubber and polyethylene foam. cloth, paper, wood,
Can be used for bonding between similar or dissimilar materials such as mortar metals.

以下に本発明を実施例により具体的に説明する。The present invention will be specifically explained below using examples.

実施例1 平均ケン化度88モルチで、平均重合度500および平
均重合度1,700の部分ケン化ポリビニルアルコール
をそれぞれ2.5重量部、1。5重量部およびノニオン
系乳化剤(ポリオキシエチレンノニルフェニルエーテル
)1.5部をエチレン以外のモノマーの合量、100重
量部に対し用いて、エチレン加圧下で乳化重合を行い、
共重合体組成エチレン15wt%、酢酸ビニル8wt%
、Veoba−10 69wt ’16、アクリル酸2
−エチルヘキシ8wt%、樹脂固形分50.5 WE%
の多元共重合体のエマルジョンを得た。このエマルジョ
ンの樹脂固形分100重量部に対しハイトランHW−3
11(大日本インキ化学(株)製、樹脂固形分45wt
%。
Example 1 2.5 parts by weight and 1.5 parts by weight of partially saponified polyvinyl alcohol with an average degree of saponification of 88 mol, an average degree of polymerization of 500 and an average degree of polymerization of 1,700, respectively, and a nonionic emulsifier (polyoxyethylene nonyl Emulsion polymerization was carried out under ethylene pressure using 1.5 parts of phenyl ether) per 100 parts by weight of the total amount of monomers other than ethylene,
Copolymer composition: ethylene 15wt%, vinyl acetate 8wt%
, Veoba-10 69wt '16, acrylic acid 2
-Ethylhexy 8 wt%, resin solid content 50.5 WE%
An emulsion of a multi-component copolymer was obtained. Hytran HW-3 per 100 parts by weight of resin solid content of this emulsion.
11 (manufactured by Dainippon Ink Chemical Co., Ltd., resin solid content 45wt)
%.

アニオン性ポリウレタンエマルジョン)を樹脂固形分換
算で15重量部添加して接着剤を調製した。この接着剤
を下記の条件で評価し、その結果を第2表に示した。
An adhesive was prepared by adding 15 parts by weight of anionic polyurethane emulsion (in terms of resin solid content). This adhesive was evaluated under the following conditions, and the results are shown in Table 2.

(1)接着条件 εP a)フレキシブルボードと手ゴム系防水シートとの接着 フレキシブルボードに接着剤を250 9/lh2塗布しオープンタイムを30分とp リキゴム系防水シートをハンドローラーで1回圧締し、
1日養生する。
(1) Adhesion conditions εP a) Adhesion of flexible board and hand rubber waterproof sheet Apply adhesive 250 9/lh2 to the flexible board and set the open time to 30 minutes. Press the liquid rubber waterproof sheet once with a hand roller. death,
Cure for one day.

b) フレキシブルボードとポリエチレンフオームとの
接着 日P 無ゴム系防水シートの代わりにポリエ チレンフオームを使用する以外はa)と同様に行う。
b) Adhesion date P of flexible board and polyethylene foam Perform in the same manner as a) except that polyethylene foam is used instead of the non-rubber waterproof sheet.

C)軟鋼板とキャンパスとの接着 脱脂した軟鋼板とキャンパス(6号) のそれぞれに接着剤を1209/−2塗布し、オープン
タイムを30分とり、接着剤の塗布面を貼合わせハンド
ローラーで1回圧締し、1日養生する。
C) Adhesion between mild steel plate and canvas Apply adhesive 1209/-2 to each of the degreased mild steel plate and canvas (No. 6), allow 30 minutes of open time, and bond the adhesive-applied surfaces together using a hand roller. Press once and cure for one day.

(2)接着力試験 り 常態剥離強度 角度180°、速度2 0 Q rrrn1分、温度2
3℃で測定した。
(2) Adhesion test Normal peel strength angle 180°, speed 20 Qrrrn 1 minute, temperature 2
Measured at 3°C.

まの状態で常態剥離強度の場合と同様に測定した。The peel strength was measured in the same manner as normal peel strength.

リ 耐熱剥離強度 温度50℃下、角度180°、速度200va/分で測
定した。
Heat resistance peel strength Measured at a temperature of 50° C., an angle of 180°, and a speed of 200 va/min.

実施例2〜5 実施例1と同様な方法で乳化重合を行い、第1表に示し
た種々のエチレンービニルエヌチル系多元共重合体エマ
ルジョンを得た。これに第1表に示すポリウレタンエマ
ルジョンをそれとれ実施例1と同様な方法で添加して接
着剤を調製し、実施例1と同様な方法で評価した。この
結果を第2表に示した。
Examples 2 to 5 Emulsion polymerization was carried out in the same manner as in Example 1 to obtain various ethylene-vinylethyl copolymer emulsions shown in Table 1. The polyurethane emulsion shown in Table 1 was added to this in the same manner as in Example 1 to prepare an adhesive, and evaluated in the same manner as in Example 1. The results are shown in Table 2.

比較例1 実施例1で得られた多元共重合体エマルシコンをそのま
ま使用し、実施例1と同様な方法で評価して第2表の結
果を得た。
Comparative Example 1 The multi-component copolymer emulsicon obtained in Example 1 was used as it was and evaluated in the same manner as in Example 1 to obtain the results shown in Table 2.

比較例2〜3 実施例1と同様な方法で乳化重合を行い第1表に示した
共重合体組成のエマルジョンを得た。これに第1表に示
すポリウレタンエマルジョンを実施例1と同様な方法で
添加して接着剤を調整し、実施例1と同様な方法で評価
した。この結果を第2表に示した。
Comparative Examples 2 to 3 Emulsion polymerization was carried out in the same manner as in Example 1 to obtain emulsions having copolymer compositions shown in Table 1. The polyurethane emulsion shown in Table 1 was added to this in the same manner as in Example 1 to prepare an adhesive, and the adhesive was evaluated in the same manner as in Example 1. The results are shown in Table 2.

Claims (1)

【特許請求の範囲】 エチレン5〜35 wt%、酢酸ビニル2〜50W【%
、高級カルボン酸ビニルエステルとアクリル酸エステル
の合計量35〜9 Q wt%を含有し、高級カルボン
酸ビニルエステルとアクリル酸エステルの重量比が10
0 : O〜60:40である共重合体組成のエチレン
−ビニルエステル系多元賜共重合体エマルジョンとポリ
ウレタンエマルジョンとを含有することを特徴とする接
着剤
[Claims] Ethylene 5-35 wt%, vinyl acetate 2-50 W[%]
, the total amount of higher carboxylic acid vinyl ester and acrylic ester is 35 to 9 Q wt%, and the weight ratio of higher carboxylic acid vinyl ester and acrylic ester is 10
An adhesive characterized by containing an ethylene-vinyl ester multi-element copolymer emulsion having a copolymer composition of 0:0 to 60:40 and a polyurethane emulsion.
JP59031129A 1984-02-20 1984-02-20 adhesive Expired - Lifetime JPH0613684B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59031129A JPH0613684B2 (en) 1984-02-20 1984-02-20 adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59031129A JPH0613684B2 (en) 1984-02-20 1984-02-20 adhesive

Publications (2)

Publication Number Publication Date
JPS60203683A true JPS60203683A (en) 1985-10-15
JPH0613684B2 JPH0613684B2 (en) 1994-02-23

Family

ID=12322812

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59031129A Expired - Lifetime JPH0613684B2 (en) 1984-02-20 1984-02-20 adhesive

Country Status (1)

Country Link
JP (1) JPH0613684B2 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997020628A1 (en) * 1995-12-07 1997-06-12 Minnesota Mining And Manufacturing Company Permeable, shaped structures of active particulate bonded with psa polymer microparticulate
SG126038A1 (en) * 2005-03-16 2006-10-30 Sumitomo Chemical Co Aqueous emulsion and method of producing the same
JP2009269956A (en) * 2008-05-01 2009-11-19 Chuo Rika Kogyo Corp Aqueous emulsion-type pressure-sensitive adhesive
WO2012169482A1 (en) * 2011-06-10 2012-12-13 住友化学株式会社 Aqueous adhesive and laminate structure
WO2012169480A1 (en) * 2011-06-10 2012-12-13 住友化学株式会社 Aqueous adhesive and laminate structure
WO2012169479A1 (en) * 2011-06-10 2012-12-13 住友化学株式会社 Aqueous adhesive and laminate structure
WO2012169481A1 (en) * 2011-06-10 2012-12-13 住友化学株式会社 Aqueous adhesive and laminate structure
JP2013151633A (en) * 2011-06-10 2013-08-08 Sumitomo Chemical Co Ltd Aqueous adhesive
CN108164650A (en) * 2017-12-26 2018-06-15 太原理工大学 Hold alkenyl non-ion aqueous polyurethane modified acrylate emulsion and preparation method thereof

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JPS5112653A (en) * 1974-06-14 1976-01-31 Siemens Ag TEIATSUHYUUZU
JPS5247833A (en) * 1975-10-15 1977-04-16 Showa Highpolymer Co Ltd Preparation of pressure sensitive adhesive composition
JPS5373235A (en) * 1976-12-10 1978-06-29 Sumitomo Chem Co Ltd Novel pressure-sensitive adhesives
JPS53134833A (en) * 1977-04-28 1978-11-24 Ito Katsuaki Waterrbase adhesives
JPS60163981A (en) * 1984-02-03 1985-08-26 Sumitomo Chem Co Ltd Adhesive composition

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JPS5112653A (en) * 1974-06-14 1976-01-31 Siemens Ag TEIATSUHYUUZU
JPS5247833A (en) * 1975-10-15 1977-04-16 Showa Highpolymer Co Ltd Preparation of pressure sensitive adhesive composition
JPS5373235A (en) * 1976-12-10 1978-06-29 Sumitomo Chem Co Ltd Novel pressure-sensitive adhesives
JPS53134833A (en) * 1977-04-28 1978-11-24 Ito Katsuaki Waterrbase adhesives
JPS60163981A (en) * 1984-02-03 1985-08-26 Sumitomo Chem Co Ltd Adhesive composition

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997020628A1 (en) * 1995-12-07 1997-06-12 Minnesota Mining And Manufacturing Company Permeable, shaped structures of active particulate bonded with psa polymer microparticulate
JP2000502281A (en) * 1995-12-07 2000-02-29 ミネソタ マイニング アンド マニュファクチャリング カンパニー A permeable, shaped structure consisting of active particles bound by pressure sensitive adhesive polymer microparticles
US6391429B1 (en) 1995-12-07 2002-05-21 3M Innovative Properties Company Permeable shaped structures of active particulate bonded with PSA polymer microparticulate
SG126038A1 (en) * 2005-03-16 2006-10-30 Sumitomo Chemical Co Aqueous emulsion and method of producing the same
JP2009269956A (en) * 2008-05-01 2009-11-19 Chuo Rika Kogyo Corp Aqueous emulsion-type pressure-sensitive adhesive
WO2012169482A1 (en) * 2011-06-10 2012-12-13 住友化学株式会社 Aqueous adhesive and laminate structure
WO2012169480A1 (en) * 2011-06-10 2012-12-13 住友化学株式会社 Aqueous adhesive and laminate structure
WO2012169479A1 (en) * 2011-06-10 2012-12-13 住友化学株式会社 Aqueous adhesive and laminate structure
WO2012169481A1 (en) * 2011-06-10 2012-12-13 住友化学株式会社 Aqueous adhesive and laminate structure
JP2013151633A (en) * 2011-06-10 2013-08-08 Sumitomo Chemical Co Ltd Aqueous adhesive
CN108164650A (en) * 2017-12-26 2018-06-15 太原理工大学 Hold alkenyl non-ion aqueous polyurethane modified acrylate emulsion and preparation method thereof
CN108164650B (en) * 2017-12-26 2020-02-21 太原理工大学 Alkenyl-terminated nonionic waterborne polyurethane modified acrylate emulsion and preparation method thereof

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