JPH01299881A - Adhesive composition - Google Patents

Adhesive composition

Info

Publication number
JPH01299881A
JPH01299881A JP13055888A JP13055888A JPH01299881A JP H01299881 A JPH01299881 A JP H01299881A JP 13055888 A JP13055888 A JP 13055888A JP 13055888 A JP13055888 A JP 13055888A JP H01299881 A JPH01299881 A JP H01299881A
Authority
JP
Japan
Prior art keywords
vinyl acetate
fiber
pts
fibrillated
desirably
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
JP13055888A
Other languages
Japanese (ja)
Other versions
JP2724719B2 (en
Inventor
Kosaku Akasaka
赤阪 公作
Takuo Ando
安藤 卓雄
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.)
Nippon Synthetic Chemical Industry Co Ltd
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 JP63130558A priority Critical patent/JP2724719B2/en
Publication of JPH01299881A publication Critical patent/JPH01299881A/en
Application granted granted Critical
Publication of JP2724719B2 publication Critical patent/JP2724719B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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

Abstract

PURPOSE:To obtain the title composition which is a nonasbestine type, has excellent adhesiveness and coatability and is useful for, e.g., bonding vinyl chloride tiles, by mixing a solution of a vinyl acetate polymer in an organic solvent with a fibrillated polyolefin fiber. CONSTITUTION:A solution if 100 pts.wt. vinyl acetate polymer such as a homopolymer of vinyl acetate or a copolymer of vinyl acetate with an olefin, an unsaturated carboxylic acid or the like in an organic solvent (e.g., methanol) is mixed with, preferably, 2-20 pts.wt. fibrillated fiber of a polyolefin which is a homopolymer of an alpha-olefin or its copolymer with a monomer (e.g., styrene), desirably, fibrillated polyolefin fiber made hydrophilic by spraying with, for example, PVA or modified by copolymerization, desirably, such fibrillated fiber having a freeness of 0.03-8sec/g and a weight-average fiber length of 0.01-2.0mm and, preferably, 100-400 pts.wt. (5-200 pts.wt. per pt.wt. fiber) inorganic filler (e.g., CaCO3) as an optional component and other additives as optional components so that the solid content of the resulting composition may be desirably 60-75wt.%.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は接着力や塗工性の改善されたノンアスベスト型
の酢酸ビニル系樹脂接着剤に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a non-asbestos vinyl acetate resin adhesive with improved adhesive strength and coatability.

[従来の技術] 酢酸ビニル系重合体有機溶剤溶液は、これに無機フィラ
ーを配合することにより比較的安価な接着剤として、例
えば塩ビタイルの接骨施工を始め、ストレート、石膏ボ
ード、木毛セメント板、ベニヤ合板、発泡スチロール板
などの貼合せ、鋳型の接着、自動車用エアフィルターエ
レメントの接着など広範な用途に使用されている。
[Prior Art] Vinyl acetate polymer organic solvent solutions can be used as relatively inexpensive adhesives by blending inorganic fillers with them, for example, for bone-bonding construction of PVC tiles, straight boards, gypsum boards, and wood-wool cement boards. It is used in a wide range of applications, including laminating veneer plywood, polystyrene foam, etc., bonding molds, and bonding air filter elements for automobiles.

し発明が解決しようとする問題点コ しかしてこの場合、無機フィラーとしてアスベストか用
いられているが、アスベストは特定化学物質に指定され
、安全衛生上の問題があるので、最近ではアスベストを
用いない処方が業界から強く要望されている。
However, in this case, asbestos is used as an inorganic filler, but asbestos is designated as a specified chemical substance and has safety and health problems, so asbestos is not used these days. Prescriptions are strongly requested by the industry.

そこでアスベストに代わる無機フィラーとして炭酸カル
シウム、クレーを始め種々のものが検討されているが、
アスベストに匹敵する、あるいはそれ以上の接着効果、
塗工性は得られていない。
Therefore, various inorganic fillers such as calcium carbonate and clay are being considered as substitutes for asbestos.
Adhesive effect comparable to or better than asbestos,
Coatability was not obtained.

[問題点を解決するための手段] 本発明者等は脱血検討の結果、酢酸ビニル系重合体(A
)の有機溶剤溶液に、ポリオレフィン系フィブリル繊維
(B)特に親木性を付与されたポリオレフィン系フィブ
リル繊維を配合した接着剤組成物が、ノンアスベスト型
の接着剤として接着力並びにクシゴテ等による塗工性に
顕著な効果を発揮し得ることを見出し本発明を完成した
[Means for Solving the Problems] As a result of blood removal studies, the present inventors discovered that vinyl acetate polymer (A
), an adhesive composition containing polyolefin fibril fibers (B), especially polyolefin fibril fibers imparted with wood-philicity, is used as a non-asbestos adhesive with adhesive strength and coating with a combing iron, etc. The present invention was completed based on the discovery that this method can have a remarkable effect on sex.

本発明の接着剤は、塩ビタイル等へ良好な接着力を示す
と共に、チクソ性も改善されクシゴテ等による塗工時に
おいて塗工操作が円滑に実施出来、塗膜面のタレ等の障
害も全く心配がない。
The adhesive of the present invention not only exhibits good adhesion to PVC tiles, etc., but also has improved thixotropy, allowing smooth coating operations when applied with a trowel, etc., and preventing problems such as sagging on the coating surface. No worries.

本発明における酢酸ビニル系重合体(A)としては、酢
酸ビニルのホモポリマーの他、酢酸ビニルとエチレン、
プロピレン、α−オクテン、α−オクタデセンなどのオ
レフィン、アクリル酸、メタクリル酸、クロトン酸、マ
レイン酸、フマール酸、イタコン酸などの不飽和カルボ
ン酸或は、その部分又は完全エステル・無水物・ニトリ
ル・アミド、ピロピオン酸ビニル、バーサチック酸ビニ
ルなどのビニルエステル、塩化ビニル、ビニルエーテル
などとの共重合体が使用されろ。異なる品種の酢酸ビニ
ル系重合体を併用することらできる。
In the present invention, the vinyl acetate polymer (A) includes a homopolymer of vinyl acetate, vinyl acetate and ethylene,
Olefins such as propylene, α-octene, α-octadecene, unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, fumaric acid, itaconic acid, or their partial or complete esters, anhydrides, nitriles, Copolymers with vinyl amide, vinyl ester such as vinyl propionate, vinyl versatate, vinyl chloride, vinyl ether, etc. may be used. Different types of vinyl acetate polymers can be used together.

有機溶剤は酢酸ビニル系重合体(A)を溶解するしので
あれば特に限定はないが、工業的に安価に入手できるメ
タノールが最も一般的に使用され、その他酢酸エチル、
エタノール、トルエン、アセトンをはじめ汎用の有機溶
剤も通常はエタノールとの併用の形で使用される。
The organic solvent is not particularly limited as long as it dissolves the vinyl acetate polymer (A), but methanol, which is industrially available at low cost, is most commonly used, and other solvents such as ethyl acetate,
Common organic solvents such as ethanol, toluene, and acetone are also commonly used in combination with ethanol.

本発明の(B)成分はポリオレフィン系フィブリル繊維
である。ポリオレフィンとしてはエチレン、プロピレン
、!−ブテン、4−メチル−1−ペンテン等のα−オレ
フィンの単独重合体の他、前記のα−オレフィンと共重
合可能なモノマー例えばスチレン、アクリロニトリル、
塩化ビニル、酢酸ビニル、アクリル酸エステル、メタク
リル酸エステルなどとの共重合体、或はこれらのブロッ
ク共重合体、グラフト共重合体等が挙げられる。
Component (B) of the present invention is polyolefin fibril fiber. Ethylene, propylene, etc. as polyolefins! In addition to homopolymers of α-olefins such as -butene and 4-methyl-1-pentene, monomers copolymerizable with the above α-olefins such as styrene, acrylonitrile,
Examples include copolymers with vinyl chloride, vinyl acetate, acrylic esters, methacrylic esters, block copolymers and graft copolymers thereof.

有利には該ポリオレフィン系フィブリル繊維は親水性が
付与される。例えばポリビニルアルコールやその誘導体
、或はデンプン、セルロース類等を繊維に噴霧したり、
又、繊維骨格中にカルボキシル基や水酸基等の親水性基
が含有される様に共重合変性しておく方法等が採用され
る。
Advantageously, the polyolefin fibril fibers are rendered hydrophilic. For example, spraying polyvinyl alcohol or its derivatives, starch, cellulose, etc. onto the fibers,
Further, a method of copolymerization modification so that hydrophilic groups such as carboxyl groups and hydroxyl groups are contained in the fiber skeleton is adopted.

該繊維としてか水係数が0.03〜8秒/g好ましくは
2〜6秒/9、重層平均繊維長が0.01〜2 、0.
m+n好ましくは0.01〜1.Ommの範囲のものが
使用される。
The fibers have a water coefficient of 0.03 to 8 seconds/g, preferably 2 to 6 seconds/9, and an average fiber length of 0.01 to 2,0.
m+n preferably 0.01 to 1. A range of 0 mm is used.

(A)と(B)との混合割合は酢酸ビニル系樹脂100
重量部に対してフィブリル繊維を2〜20重量部、特に
8〜15重量部で用いるのが好ましい。
The mixing ratio of (A) and (B) is vinyl acetate resin 100%
It is preferred to use 2 to 20 parts by weight, especially 8 to 15 parts by weight, of fibril fibers.

(B)が2重量部以下では本発明の効果が得難く、一方
20重量部以上では系がゲル化状態となり実用性が低下
する。
If (B) is less than 2 parts by weight, it is difficult to obtain the effects of the present invention, while if it is more than 20 parts by weight, the system becomes gelled and practicality is reduced.

本発明の接着剤にはその他必要に応じ他の無機フィラー
、ロジン、ロジン誘導体などの他の接着性樹脂、繊維類
、着色剤、可塑剤、界面活性剤、可使時間延長剤などを
配合してもよい。又有機溶剤に対し2割程度又はそれ以
下の水を添加してもよい。
The adhesive of the present invention may contain other inorganic fillers, other adhesive resins such as rosin and rosin derivatives, fibers, colorants, plasticizers, surfactants, pot life extenders, etc., as necessary. You can. Also, water may be added to the organic solvent in an amount of about 20% or less.

特に無機フィラーとして炭酸カルシウムやクレー、タル
ク、酸化チタン等の併用は有利となる。
In particular, it is advantageous to use calcium carbonate, clay, talc, titanium oxide, etc. as an inorganic filler.

該フィラーは酢酸ビニル系樹脂の100重量部に対して
100〜400重量部程度、ポ置部レフィン系フィブリ
ル繊維の重量に対して5〜200倍の割合で用いられろ
The filler is used in an amount of about 100 to 400 parts by weight per 100 parts by weight of the vinyl acetate resin, and 5 to 200 times the weight of the refin-based fibril fibers.

接着剤組成物の固形分含量は塗工性等の作業性の点で6
0〜75重量%程度である。
The solid content of the adhesive composition is 6.
It is about 0 to 75% by weight.

[作  用コ 本発明の接着剤組成物はノンアスベスト型としてその需
要が増々拡大すると共に、接着力や塗工性に優れるため
広い面積の接着施工、例えば尺角の塩ビタイル接着や長
尺タイルの接着施工等に好適に使用される。
[Function] The demand for the adhesive composition of the present invention is increasing as it is a non-asbestos type, and because of its excellent adhesive strength and coating properties, it is suitable for adhesive construction of large areas, such as adhesion of rectangular PVC tiles and long tiles. Suitable for use in adhesive construction, etc.

[実施例J 次に例を挙げて本発明の接着剤を更に説明する。以下「
部」、「%」とあるのは重量基準で表したものである。
[Example J] Next, the adhesive of the present invention will be further explained with reference to an example. below"
"parts" and "%" are expressed on a weight basis.

実施例1 重合度+000のポリ酢酸ビニル100部とメタノール
100部とよりなるペースト200部に、が水係数3秒
/9、重量平均繊維長0 、8 mmのポリエチレンフ
ィブリル繊維(ポリビニルアルコールで親水性付与され
たもの)10部、炭酸カルシウム200部及びメタノー
ル50部を添加して接着剤を調製した。
Example 1 200 parts of a paste consisting of 100 parts of polyvinyl acetate with a polymerization degree of +000 and 100 parts of methanol were mixed with polyethylene fibril fibers (hydrophilic with polyvinyl alcohol) having a water coefficient of 3 seconds/9, a weight average fiber length of 0, and 8 mm. 200 parts of calcium carbonate and 50 parts of methanol were added to prepare an adhesive.

この接着剤を用いて常態接着力、チクソ係数、塗工性を
測定した。結果を第1表に示す。
Using this adhesive, normal adhesive strength, thixoscopic coefficient, and coatability were measured. The results are shown in Table 1.

尚、測定方法は次のとうりである。The measurement method is as follows.

常態接着カニカバ材にクシゴテで塗工し、カバ材を指圧
圧着し、接着部が25X25mmのテストピースを作り
、20℃×1日養 生後、オートグラフにより引張速度 20mm/minで接着力を測定する (測定雰囲気は20℃×65%RH) チクソ係数二BH型粘度計を用い2 Orpm時の粘度
に対する2 rpm時の粘度比 塗 工 性:JIS  A3536に準じ標準クシゴテ
で接着剤をスレート板上に塗工し、 塗り易さと、クシ目出の状態を観察す る。
Apply the product to normally adhesive crab birch wood using a comb trowel, press the birch wood with finger pressure, make a test piece with a bonded area of 25 x 25 mm, and after curing at 20°C for 1 day, measure the adhesive force using an autograph at a tensile speed of 20 mm/min. (Measurement atmosphere: 20°C x 65% RH) Thixo coefficient 2 BH type viscometer was used to determine the viscosity ratio at 2 rpm to the viscosity at 2 orpm.Coating property: Apply the adhesive onto the slate board using a standard combing iron according to JIS A3536. and observe the ease of application and the appearance of combs.

対照例1〜2 ポリエチレンフィブリル繊維の使用を省略した(対照例
1)以外及びポリエチレンブイプリル繊維に代えてアス
ベスト(ノザワ社製のアスベストテーリング)を用いた
以外(対照例2)は実施例1と同一の方法を行った。
Control Examples 1 to 2 Example 1 except that the use of polyethylene fibril fibers was omitted (Control Example 1) and asbestos (Asbestos Tailing manufactured by Nozawa Co., Ltd.) was used in place of the polyethylene fibril fibers (Control Example 2). The same method was followed.

第1表に結果を示す。Table 1 shows the results.

実施例2〜6 第1表に示す接着剤を実施例1に準じて調製しその性質
を調べた。結果を第1表に併せて示す。
Examples 2 to 6 Adhesives shown in Table 1 were prepared according to Example 1 and their properties were investigated. The results are also shown in Table 1.

[効  果] 本発明の接着剤は優れた接着力、塗工性を示すノンアス
ベスト型接着剤である。
[Effects] The adhesive of the present invention is a non-asbestos adhesive that exhibits excellent adhesive strength and coatability.

Claims (1)

【特許請求の範囲】 1、酢酸ビニル系重合体(A)の有機溶剤溶液にポリオ
レフィン系フィブリル繊維(B)を配合してなる接着剤
組成物。 2、親水性が付与されたポリオレフィン系フィブリル繊
維を用いることを特徴とする特許請求の範囲第1項記載
の接着剤組成物。
[Claims] 1. An adhesive composition prepared by blending polyolefin fibril fibers (B) into an organic solvent solution of a vinyl acetate polymer (A). 2. The adhesive composition according to claim 1, which uses polyolefin fibril fibers imparted with hydrophilic properties.
JP63130558A 1988-05-27 1988-05-27 Adhesive composition Expired - Fee Related JP2724719B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63130558A JP2724719B2 (en) 1988-05-27 1988-05-27 Adhesive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63130558A JP2724719B2 (en) 1988-05-27 1988-05-27 Adhesive composition

Publications (2)

Publication Number Publication Date
JPH01299881A true JPH01299881A (en) 1989-12-04
JP2724719B2 JP2724719B2 (en) 1998-03-09

Family

ID=15037136

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63130558A Expired - Fee Related JP2724719B2 (en) 1988-05-27 1988-05-27 Adhesive composition

Country Status (1)

Country Link
JP (1) JP2724719B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04127241U (en) * 1991-05-14 1992-11-19 矢崎総業株式会社 adhesive composition
WO2013126377A1 (en) * 2012-02-23 2013-08-29 3M Innovative Properties Company Structural acrylic adhesive

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60250079A (en) * 1984-05-28 1985-12-10 Daicel Chem Ind Ltd Adhesive composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60250079A (en) * 1984-05-28 1985-12-10 Daicel Chem Ind Ltd Adhesive composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04127241U (en) * 1991-05-14 1992-11-19 矢崎総業株式会社 adhesive composition
WO2013126377A1 (en) * 2012-02-23 2013-08-29 3M Innovative Properties Company Structural acrylic adhesive
CN104220542A (en) * 2012-02-23 2014-12-17 3M创新有限公司 Structural acrylic adhesive
US9416299B2 (en) 2012-02-23 2016-08-16 3M Innovative Properties Company Structural acrylic adhesive

Also Published As

Publication number Publication date
JP2724719B2 (en) 1998-03-09

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