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JPS6251309B2 - - Google Patents
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JPS6251309B2 - - Google Patents

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Publication number
JPS6251309B2
JPS6251309B2 JP15878879A JP15878879A JPS6251309B2 JP S6251309 B2 JPS6251309 B2 JP S6251309B2 JP 15878879 A JP15878879 A JP 15878879A JP 15878879 A JP15878879 A JP 15878879A JP S6251309 B2 JPS6251309 B2 JP S6251309B2
Authority
JP
Japan
Prior art keywords
vinyl acetate
weight
adhesive
methanol
paste
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
Application number
JP15878879A
Other languages
Japanese (ja)
Other versions
JPS5681381A (en
Inventor
Tsutomu Mori
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.)
Mitsubishi Chemical Corp
Original Assignee
Nippon Synthetic Chemical Industry 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 Nippon Synthetic Chemical Industry Co Ltd filed Critical Nippon Synthetic Chemical Industry Co Ltd
Priority to JP15878879A priority Critical patent/JPS5681381A/en
Publication of JPS5681381A publication Critical patent/JPS5681381A/en
Publication of JPS6251309B2 publication Critical patent/JPS6251309B2/ja
Granted legal-status Critical Current

Links

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  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は酢酸ビニル系共重合体をビヒクルとす
る建材用溶剤型接着剤に関するものである。 ポリ酢酸ビニルをビヒクルとするメタノールペ
ーストは、安価でかつ比較的広範な被着体に良好
な接着性を有するため、建築内装用などの用途に
用いる溶剤型接着剤として広く知られているが、
初期接着性が必ずしも充分でないため、天井材の
接着においては釘の併用が、木レンガなどの接着
においては粘着テープなどによる仮止めが、床材
の接着においては目地部分の浮き上り防止のため
の砂袋の使用がそれぞれ必要となり、作業が煩雑
となる不利がある。そこでこのような欠点を改良
すべく、従来よりロジン或いはフエノール樹脂系
タツキフアイアーの添加、可塑剤の添加など添加
剤による改良が試みられているが、未だ充分とは
言えない。 本発明は酢酸ビニル系重合体中に特定の成分を
共重合することにより、上記の如き従来の溶剤型
接着剤のもつ欠点を改良したものである。 本発明の溶剤型接着剤は、酢酸ビニル(A)80〜
99.9重量%、ジアリルフタレート、ジエチレング
リコールジメタクリレート、トリメチロールプロ
パントリアクリレートという特定の化合物から選
ばれる分子中に2個以上の重合体不飽和基を有す
るモノマー(B)0.1〜10重量%及び上記以外のビニ
ルモノマー(C)0〜19.9重量%よりなる組成を有す
る酢酸ビニル系共重合体(X)のメタノール溶液
をビヒクルとしてなるものであり、建材用の被着
体に対する初期接着力が顕著に向上するという効
果を奏する。 本発明において用いる酢酸ビニル系共重合体
(X)は上記のように 酢酸ビニル(A) 80〜99.9重量% 分子中に2個以上の重合性不飽和基を有するモ
ノマー(B) 0.1〜10重量% 上記以外のビニルモノマー(C) 0〜19.9重量% の各成分よりなる。 酢酸ビニル(A)成分は共重合体の主成分であり、
その共重合割合が80重量%未満では接着力自体が
不足し、一方99.9重量%を越すことは、相対的に
(B)成分が少なくなりすぎることになるので、初期
接着力向上効果が期待できない。 分子中に2個以上の重合性不飽和基を有するモ
ノマー(B)成分は改質成分であり、その共重合割合
が0.1重量%未満では初期接着力向上効果が充分
に奏されず、一方その割合が10重量%を越える場
合は得られるペーストがゲル化傾向を示し、実用
に供しがたくなる。特に好ましい範囲は0.1〜5
重量%である。かかる(B)成分としては、ジアリル
フタレート、エチレングリコールジメタクリレー
ト、トリメチロールプロパントリアクリレート、
などがあげられる。これらは2種以上を併用する
こともできる。 本発明の酢酸ビニル系共重合体は上記(A)及び(B)
の2成分からなるが、この2成分以外に最大19.9
重量%までの範囲で残余として上記以外のビニル
モノマー(C)を含んでいてもよい。(C)成分が19.9重
量%を越えることは、酢酸ビニル系共重合体のも
つ接着性、低価格性、メタノール可溶性などの特
質が損われるので避けるべきである。かかる(C)成
分としては、アクリル酸、メタクリル酸、クロト
ン酸等の不飽和モノカルボン酸又はそのアルキル
エステルや塩、マレイン酸、フマール酸、イタコ
ン酸などの不飽和ジカルボン酸又はそのモノアル
キルエステルやジアルキルエステルや無水物や
塩、アクリロニトリルやメタクリロニトリル、ア
クリルアミドやメタクリルアミド、プロピオン酸
ビニル、ステアリン酸ビニル、バーサチツク酸ビ
ニル等酢酸ビニル以外のビニルエステル、塩化ビ
ニル、炭素数2〜20或いはそれ以上のオレフイン
などがあげられる。 本発明の接着剤はビヒクルとして上記酢酸ビニ
ル系共重合体(X)を用いるほか、充填剤(Y)
及び有機溶剤としてメタノールを用いる。 充填剤(Y)としては、石綿、炭酸カルシウ
ム、クレー、タルク、酸化チタン、フライアツシ
ユをはじめとする各種の充填剤が用いられる。充
填剤(Y)の配合量は特に限定はないが、酢酸ビ
ニル系共重合体(X)に対し重量で20〜500重量
%の範囲から選ぶことが多い。 本発明の接着剤には上記(X),(Y)及びメタ
ノールの各成分のほか、さらに必要に応じてロジ
ン、ロジン誘導体、上記(B)成分を含まないポリ酢
酸ビニル又は酢酸ビニル共重合体、可塑剤、着色
剤などを適当量配合してもよい。又有機溶剤に対
し2割程度以下の量の水が存在していても差支え
ない。 本発明の建材用接着剤は床面、壁面、天井面等
の接着施工、たとえば塩ビタイルの接着、長尺タ
イルの接着、胴ぶちの接着、木レンガの接着、プ
ラスチツクスシートの接着、吸音ボードの接着な
どに利用される。 次に例をあげて本発明の溶剤型接着剤をさらに
説明する。以下「部」、「%」とあるのは重量基準
で表わしたものである。又ペーストの粘度は25℃
における測定値である。 例 1 酢酸ビニル99.7部及びジアリフタレート0.3部
をメタノール100部中で常法により溶液重合して
酢酸ビニル系共重合体濃度50%、粘度10000cps
のメタノールペーストを得た。 このペースト200部に石綿140部、炭酸カルシウ
ム60部及びメタノール80部を添加混合して接着剤
を調製した。 この接着剤をクシゴテを用いてスレート板上に
塗布し、硬質塩化ビニル樹脂板を指圧接着した後
直ちに引張接着強度を測定した。 又この接着剤をクシゴテを用いてコンクリート
床面上に約300g/m2となるように塗布した後高
反ばつ性床タイルを貼りつけ、その後は特に荷重
を加えることなく放置、乾燥したが、目地部の浮
き上がりは全く認められなかつた。 以上の結果を第1表に示す。 対照例 1 重合体濃度49.8%、粘度10300cpsの酢酸ビニル
ホモポリマーのメタノールペーストを用いたほか
は例1と同様にして接着剤の調製を行い、引張接
着強度の測定と高反ばつ性床タイルの接着施工を
行つた。 結果を第1表に合せて示す。
The present invention relates to a solvent-based adhesive for building materials that uses a vinyl acetate copolymer as a vehicle. Methanol paste using polyvinyl acetate as a vehicle is widely known as a solvent-based adhesive used for applications such as building interiors because it is inexpensive and has good adhesion to a relatively wide range of adherends.
Because the initial adhesion is not always sufficient, nails are used in conjunction with ceiling materials, temporary fixing with adhesive tape is used to adhere wooden bricks, etc., and adhesive tape is used to prevent joints from lifting when adhering flooring materials. Each method requires the use of sandbags, which has the disadvantage of complicating the work. In order to overcome these drawbacks, attempts have been made to use additives such as the addition of rosin or phenolic resin tackifiers and plasticizers, but these improvements have not yet been sufficient. The present invention improves the above-mentioned drawbacks of conventional solvent-based adhesives by copolymerizing specific components into a vinyl acetate polymer. The solvent-based adhesive of the present invention contains vinyl acetate (A) 80~
99.9% by weight, 0.1 to 10% by weight of a monomer (B) having two or more polymeric unsaturated groups in the molecule selected from specific compounds diallyl phthalate, diethylene glycol dimethacrylate, trimethylolpropane triacrylate, and other than the above. It is made using a methanol solution of vinyl acetate copolymer (X) having a composition consisting of 0 to 19.9% by weight of vinyl monomer (C) as a vehicle, and the initial adhesive strength to adherends for building materials is significantly improved. This effect is achieved. The vinyl acetate copolymer (X) used in the present invention is as described above: Vinyl acetate (A) 80 to 99.9% by weight Monomer (B) having two or more polymerizable unsaturated groups in the molecule 0.1 to 10% by weight % Vinyl monomer (C) other than the above 0 to 19.9% by weight of each component. Vinyl acetate (A) component is the main component of the copolymer,
If the copolymerization ratio is less than 80% by weight, the adhesive strength itself will be insufficient, while if it exceeds 99.9% by weight, it will be relatively
Since the amount of component (B) will be too small, no effect on improving initial adhesive strength can be expected. The monomer (B) component having two or more polymerizable unsaturated groups in the molecule is a modifying component, and if its copolymerization ratio is less than 0.1% by weight, the initial adhesion strength improvement effect will not be sufficiently exhibited; When the proportion exceeds 10% by weight, the resulting paste tends to gel, making it difficult to put it to practical use. Particularly preferred range is 0.1 to 5
Weight%. Such component (B) includes diallyl phthalate, ethylene glycol dimethacrylate, trimethylolpropane triacrylate,
etc. Two or more of these can also be used in combination. The vinyl acetate copolymer of the present invention has the above (A) and (B)
It consists of two components, but in addition to these two components, there is a maximum of 19.9
Vinyl monomers (C) other than those mentioned above may be included as a remainder within a range of up to % by weight. A content of component (C) in excess of 19.9% by weight should be avoided since the properties of the vinyl acetate copolymer, such as adhesiveness, low cost, and methanol solubility, will be impaired. Component (C) includes unsaturated monocarboxylic acids such as acrylic acid, methacrylic acid, and crotonic acid, or alkyl esters and salts thereof; unsaturated dicarboxylic acids such as maleic acid, fumaric acid, and itaconic acid, and monoalkyl esters thereof; Dialkyl esters, anhydrides and salts, acrylonitrile and methacrylonitrile, acrylamide and methacrylamide, vinyl esters other than vinyl acetate such as vinyl propionate, vinyl stearate, vinyl versatate, vinyl chloride, carbon atoms of 2 to 20 or more Examples include olefin. The adhesive of the present invention uses the above-mentioned vinyl acetate copolymer (X) as a vehicle, as well as a filler (Y).
and methanol is used as an organic solvent. As the filler (Y), various fillers including asbestos, calcium carbonate, clay, talc, titanium oxide, and fly ash are used. The amount of the filler (Y) to be blended is not particularly limited, but it is often selected from a range of 20 to 500% by weight based on the vinyl acetate copolymer (X). In addition to the above components (X), (Y), and methanol, the adhesive of the present invention may further include rosin, a rosin derivative, and polyvinyl acetate or vinyl acetate copolymer that does not contain the above component (B). , a plasticizer, a coloring agent, etc. may be added in appropriate amounts. Further, there is no problem even if water is present in an amount of about 20% or less relative to the organic solvent. The adhesive for building materials of the present invention can be used for adhesion of floors, walls, ceilings, etc., such as adhesion of PVC tiles, adhesion of long tiles, adhesion of body edges, adhesion of wooden bricks, adhesion of plastic sheets, and sound absorption boards. Used for adhesion, etc. Next, the solvent-based adhesive of the present invention will be further explained with reference to examples. Hereinafter, "parts" and "%" are expressed on a weight basis. Also, the viscosity of the paste is 25℃
This is the measured value at . Example 1 99.7 parts of vinyl acetate and 0.3 parts of dialiphthalate were solution polymerized in 100 parts of methanol by a conventional method to obtain a vinyl acetate copolymer concentration of 50% and a viscosity of 10,000 cps.
A methanol paste was obtained. An adhesive was prepared by adding and mixing 140 parts of asbestos, 60 parts of calcium carbonate, and 80 parts of methanol to 200 parts of this paste. This adhesive was applied onto a slate board using a trowel, and the hard vinyl chloride resin board was bonded with finger pressure, and the tensile adhesive strength was immediately measured. In addition, this adhesive was applied to the concrete floor surface using a trowel at a concentration of approximately 300 g/m 2 , and then high-resilience floor tiles were attached, and then left to dry without applying any particular load. No lifting of the joint was observed at all. The above results are shown in Table 1. Control Example 1 An adhesive was prepared in the same manner as in Example 1 except that a methanol paste of vinyl acetate homopolymer with a polymer concentration of 49.8% and a viscosity of 10,300 cps was used. Adhesive construction was performed. The results are also shown in Table 1.

【表】 例2〜4、対照例2〜4 下記重合体のメタノールペーストを用いたほか
は例1と同様にして接着剤を調製し、引張接着強
度の測定と高反ばつ性床タイルの接着施工を行つ
た。 例 2 酢酸ビニル95%及びエチレングリコールジメタ
クリレート5%よりなる組成の共重合体の濃度
48.5%、粘度3000cpsのメタノールペースト。 対照例 2 酢酸ビニルホモポリマーの濃度50%、粘度
30000cpsのメタノールペースト。 例 3 酢酸ビニル87.5%、ジアリルフタレート0.5%
及びエチレン12%よりなる組成の共重合体の濃度
45%、粘度6000cpsのメタノールペースト。 対照例 3 酢酸ビニル87%及びエチレン13%よりなる組成
の共重合体の濃度47%、粘度8000cpsのメタノー
ルペースト。 例 4 酢酸ビニル79%、トリメチロールプロパントリ
アクリレート1%及びアクリル酸エチル20%より
なる組成の共重合体の濃度48%、粘度9800cpsの
メタノールペーストに対照例1の酢酸ビニルホモ
ポリマーの濃度49.8%、粘度10300cpsのメタノー
ルペーストを重量比70:30の割合で混合した混合
ペースト。 対照例 4 酢酸ビニル80%及びアクリル酸エチル20%より
なる組成の共重合体の濃度50%、粘度6000cpsの
メタノールペーストに対照例1の酢酸ビニルホモ
ポリマーの濃度49.8%、粘度10300cpsのメタノー
ルペーストを重量比70:30の割合で混合した混合
ペースト。 以上例2〜4、対照例2〜4の結果を第2表に
示す。
[Table] Examples 2 to 4, Control Examples 2 to 4 Adhesives were prepared in the same manner as in Example 1 except that methanol paste of the following polymer was used, and the tensile adhesive strength was measured and the adhesion of high resilience floor tiles was performed. carried out the construction. Example 2 Concentration of a copolymer with a composition of 95% vinyl acetate and 5% ethylene glycol dimethacrylate
Methanol paste with 48.5% and viscosity of 3000cps. Control example 2 Vinyl acetate homopolymer concentration 50%, viscosity
30000cps methanol paste. Example 3 Vinyl acetate 87.5%, diallyl phthalate 0.5%
and the concentration of a copolymer with a composition consisting of 12% ethylene.
45% methanol paste with a viscosity of 6000 cps. Control Example 3 Methanol paste with a concentration of 47% and a viscosity of 8000 cps of a copolymer consisting of 87% vinyl acetate and 13% ethylene. Example 4 A copolymer of 79% vinyl acetate, 1% trimethylolpropane triacrylate and 20% ethyl acrylate has a concentration of 48% and a methanol paste with a viscosity of 9800 cps has a concentration of 49.8% of the vinyl acetate homopolymer of Control Example 1. , a mixed paste made by mixing methanol paste with a viscosity of 10,300 cps at a weight ratio of 70:30. Control Example 4 Methanol paste of the vinyl acetate homopolymer of Control Example 1 with a concentration of 49.8% and a viscosity of 10,300 cps was added to a methanol paste of a copolymer with a composition of 80% vinyl acetate and 20% ethyl acrylate with a concentration of 50% and a viscosity of 6000 cps. Mixed paste mixed at a weight ratio of 70:30. The results of Examples 2 to 4 and Control Examples 2 to 4 are shown in Table 2.

【表】 例 5 酢酸ビニル89.5%、ジアリルフタレート0.5%
及びメタクリル酸メチル10%よりなる共重合体の
濃度50%、粘度35000cpsのメタノールペースト
200部に石綿150部及びメタノール50部を添加混合
して接着剤を調製し、コンクリート面に木レンガ
を接着した。 対照例 5 酢酸ビニル90%及びメタクリル酸メチル10%よ
りなる共重合体の濃度50%、粘度40000cpsのメ
タノールペーストを用いたほかは例5と同様にし
て接着剤を調製し、コンクリート面と木レンガと
の接着を行つた。 例 6 酢酸ビニル82%、エチレングリコールジメタク
リレート8部及びバーサチツク酸ビニル10%より
なる共重合体の濃度50%、粘度15000cpsのメタ
ノールペーストを用いたほかは例5と同様にして
接着剤を調製し、コンクリート面と木レンガとの
接着を行つた。 対照例 6 酢酸ビニル90%及びバーサチツク酸ビニル10%
よりなる共重合体の濃度50%、粘度17000cpsの
メタノールペーストを用いたほかは例5と同様に
して接着剤を調製し、コンクリート面と木レンガ
との接着を行つた。 以上例5〜6、対照例5〜6の引張接着強度は
次の如くであつた。 例5 3.21Kg/25mm×25mm 対照例5 1.93Kg/25mm/25mm 例6 3.15Kg/25mm×25mm 対照例6 1.90Kg/25mm×25mm
[Table] Example 5 Vinyl acetate 89.5%, diallyl phthalate 0.5%
Methanol paste with a copolymer concentration of 50% and a viscosity of 35,000 cps consisting of 10% and methyl methacrylate.
An adhesive was prepared by adding and mixing 200 parts of asbestos, 150 parts of asbestos, and 50 parts of methanol, and wooden bricks were adhered to the concrete surface. Control Example 5 An adhesive was prepared in the same manner as in Example 5 except that methanol paste with a concentration of 50% copolymer consisting of 90% vinyl acetate and 10% methyl methacrylate and a viscosity of 40,000 cps was used, and was applied to a concrete surface and a wooden brick. Gluing was performed with Example 6 An adhesive was prepared in the same manner as in Example 5, except that methanol paste with a 50% concentration of a copolymer consisting of 82% vinyl acetate, 8 parts ethylene glycol dimethacrylate, and 10% vinyl versatate and a viscosity of 15,000 cps was used. , the concrete surface and the wooden brick were bonded together. Control example 6 90% vinyl acetate and 10% vinyl versatile acid
An adhesive was prepared in the same manner as in Example 5, except that a methanol paste with a copolymer concentration of 50% and a viscosity of 17,000 cps was used to bond the concrete surface and the wooden bricks. The tensile adhesive strengths of Examples 5 and 6 and Control Examples 5 and 6 were as follows. Example 5 3.21Kg/25mm×25mm Control example 5 1.93Kg/25mm×25mm Example 6 3.15Kg/25mm×25mm Control example 6 1.90Kg/25mm×25mm

Claims (1)

【特許請求の範囲】 1 酢酸ビニル(A)80〜99.9重量%、ジアリルフタ
レート、ジエチレングリコールジメタクリレー
ト、トリメチロールプロパントリアクリレートか
ら選ばれる分子中に2個以上の重合性不飽和基を
有するモノマー(B)0.1〜10重量%及び上記以外の
ビニルモノマー(C)0〜19.9重量%よりなる組成を
有する酢酸ビニル系共重合体(X)のメタノール
溶液をビヒクルとしてなる建材用溶剤型接着剤。 2 酢酸ビニル系共重合体(X)をビヒクルと
し、充填剤(Y)及び有機溶剤(Z)を含む特許
請求の範囲第1項記載の接着剤。 3 充填剤(Y)がアスベスト又は炭酸カルシウ
ムである特許請求の範囲第2項記載の接着剤。
[Scope of Claims] 1. A monomer (B) having two or more polymerizable unsaturated groups in the molecule selected from 80 to 99.9% by weight of vinyl acetate (A), diallyl phthalate, diethylene glycol dimethacrylate, and trimethylolpropane triacrylate. ) A solvent-based adhesive for building materials, which is made of a methanol solution of a vinyl acetate copolymer (X) having a composition of 0.1 to 10% by weight and 0 to 19.9% by weight of a vinyl monomer (C) other than the above. 2. The adhesive according to claim 1, which contains a vinyl acetate copolymer (X) as a vehicle, a filler (Y), and an organic solvent (Z). 3. The adhesive according to claim 2, wherein the filler (Y) is asbestos or calcium carbonate.
JP15878879A 1979-12-06 1979-12-06 Solvent type adhesive Granted JPS5681381A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15878879A JPS5681381A (en) 1979-12-06 1979-12-06 Solvent type adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15878879A JPS5681381A (en) 1979-12-06 1979-12-06 Solvent type adhesive

Publications (2)

Publication Number Publication Date
JPS5681381A JPS5681381A (en) 1981-07-03
JPS6251309B2 true JPS6251309B2 (en) 1987-10-29

Family

ID=15679346

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15878879A Granted JPS5681381A (en) 1979-12-06 1979-12-06 Solvent type adhesive

Country Status (1)

Country Link
JP (1) JPS5681381A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2733633B2 (en) * 1991-03-27 1998-03-30 東リ株式会社 Solvent adhesive

Also Published As

Publication number Publication date
JPS5681381A (en) 1981-07-03

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