JPS59172569A - Aerosol type spraying adhesive - Google Patents
Aerosol type spraying adhesiveInfo
- Publication number
- JPS59172569A JPS59172569A JP4843083A JP4843083A JPS59172569A JP S59172569 A JPS59172569 A JP S59172569A JP 4843083 A JP4843083 A JP 4843083A JP 4843083 A JP4843083 A JP 4843083A JP S59172569 A JPS59172569 A JP S59172569A
- Authority
- JP
- Japan
- Prior art keywords
- ethylene
- vinyl acetate
- adhesive
- acetate copolymer
- tackifier
- 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
Links
Landscapes
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【発明の詳細な説明】 本発明は、エアゾル型スプレー接着剤に関する。[Detailed description of the invention] The present invention relates to an aerosol spray adhesive.
従来周知の通り、エチレン−酢酸ビニル共重合体は、エ
チレン共重合量が通常70重量%以上のものは、主にホ
ットメルト型接着剤の原料として使用され、製本や木工
業界等に広く利用されている。又、エチレン共重合量が
通常20重量パーセント以下の共重合体は、主にエマル
ジョン型接着剤の原料として使用され、軟質塩化ビニル
シートのラミネートや、樹脂加工紙等の貼り合せに広く
利用されている。As is well known, ethylene-vinyl acetate copolymers with an ethylene copolymerization amount of 70% by weight or more are mainly used as raw materials for hot-melt adhesives and are widely used in the bookbinding and woodworking industries. ing. In addition, copolymers with an ethylene copolymerization amount of 20% by weight or less are mainly used as raw materials for emulsion-type adhesives, and are widely used for laminating soft vinyl chloride sheets and bonding resin-treated paper, etc. There is.
本発明者は、これらエチレン−酢酸ビニル共重合体の接
着剤としての特性をエアゾル型接着剤に応用するため、
鋭意研究の結果、特定の共重合割合のエチレン−酢酸ビ
ニル共重合体に、粘着付与剤、有機溶媒、及び噴射剤を
配合することにより、優れたエアゾル型スプレー接着剤
が得られることを見い出し本発明を完成するに至った。In order to apply the adhesive properties of these ethylene-vinyl acetate copolymers to an aerosol type adhesive, the present inventors
As a result of intensive research, it was discovered that an excellent aerosol type spray adhesive can be obtained by blending a tackifier, an organic solvent, and a propellant with a specific copolymerization ratio of ethylene-vinyl acetate copolymer. The invention was completed.
すなわち、本発明は、20〜70重量%のエチレンと8
0〜80重量%の酢酸ビニルとのエチレン−酢酸ビニル
共重合体、粘着付与剤、有機溶媒及び噴射剤を主成分と
するエアゾル型スプレー接着剤に係るものである。That is, in the present invention, 20 to 70% by weight of ethylene and 8
This invention relates to an aerosol type spray adhesive whose main components are an ethylene-vinyl acetate copolymer with 0 to 80% by weight of vinyl acetate, a tackifier, an organic solvent, and a propellant.
本発明に於いて使用するエチレン−酢酸ビニル共重合体
は、エチレンが20〜70重量%含まれているものであ
るが、このようなエチレン含有量の上記共重合体は、従
来殆んど使用されておらず、たとえばインクの改質剤や
ホットメルト型接着剤の改質剤等としてわずかに使用さ
れているにすぎない。The ethylene-vinyl acetate copolymer used in the present invention contains 20 to 70% by weight of ethylene, but the above copolymers with such an ethylene content have rarely been used in the past. For example, it is only used to a small extent as a modifier for ink or a modifier for hot-melt adhesives.
るものを使用する必要があり、この際エチレンの量が2
0重量%に達しない場合は、接着剤としてスプレー塗付
した場合に、得られる接着剤塗付被膜のコンタクト性が
乏しく、また有機溶媒及び噴射剤との混合が不安定で満
足するものが出来ない。In this case, the amount of ethylene must be 2
If it does not reach 0% by weight, the contact properties of the resulting adhesive film will be poor when spray applied as an adhesive, and the mixture with the organic solvent and propellant will be unstable and unsatisfactory. do not have.
本発明に用いるエチレン−酢酸ビニル共重合体は、有機
溶媒に可溶性であり、適度のゴム弾性を示し、有機溶媒
溶液を噴射剤と共にエアゾル容器に充填し、スプレーし
た時に、スプレーパターン面積の広い、換言すれば、充
分に霧化したエアゾルスプレー状態が得られ、塗付され
た接着剤被膜は、エラストマー型接着剤のコンタクト性
に四速する優れたコンタクト性を示し、且つまた優れた
接着性を有している。The ethylene-vinyl acetate copolymer used in the present invention is soluble in organic solvents, exhibits appropriate rubber elasticity, and when an aerosol container is filled with an organic solvent solution together with a propellant and sprayed, a wide spray pattern area can be obtained. In other words, a well-atomized aerosol spray state is obtained, and the applied adhesive film exhibits excellent contact properties that are four times faster than those of elastomeric adhesives, and also has excellent adhesive properties. have.
本発明に使用する粘着付与剤は、接着剤塗付被膜の粘着
保持性と良好な接着性能を得るために使用されるもので
あり、たとえばロジン誘導体、チルヘン系樹脂、オレフ
ィンまたはジオレフィン重合体、シクロペンタジェン樹
脂、フェノール樹脂、スチレン系樹脂、クマロン−イン
デン樹脂、ポリアミド等が例示出来、その他脂環族飽和
炭化水素樹脂、芳香族炭化水素樹脂、脂環族不飽和炭化
水素樹脂等も使用され、これ等は1種又は2種以上が使
用される。これ等粘着付与剤は上記エチレン−酢酸ビニ
ル共重合体10o重量部に対し5〜200重量部程度使
用される。The tackifier used in the present invention is used to obtain adhesive retention and good adhesive performance of the adhesive coating, and includes, for example, rosin derivatives, chirhenic resins, olefin or diolefin polymers, Examples include cyclopentadiene resin, phenolic resin, styrene resin, coumaron-indene resin, polyamide, etc. Other examples include alicyclic saturated hydrocarbon resin, aromatic hydrocarbon resin, alicyclic unsaturated hydrocarbon resin, etc. , these may be used alone or in combination of two or more. These tackifiers are used in an amount of about 5 to 200 parts by weight per 10 parts by weight of the ethylene-vinyl acetate copolymer.
本発明に於いて用いる有−溶媒としては、エチレン−酢
酸ビニル共重合体及び粘着付与剤の両者を溶解し得るも
のであれば良く、たとえばトルエン、キシレン等の芳香
族炭化水素類、n−ヘキサン、シクロへ牛サン等の脂肪
族炭化水素類、塩化メチレン、1−1−1−トリクロル
エタン、トリクロルエチレン等の塩素化炭化水素類、ア
セトン。The solvent used in the present invention may be any solvent as long as it can dissolve both the ethylene-vinyl acetate copolymer and the tackifier, such as aromatic hydrocarbons such as toluene and xylene, and n-hexane. , aliphatic hydrocarbons such as cyclohexane, chlorinated hydrocarbons such as methylene chloride, 1-1-1-trichloroethane, trichlorethylene, and acetone.
メチルエチルケトン等のケトン類、酢酸エチル等のエス
テル類等をあげることができ、本発明に詔いては、これ
らの有機溶媒を使用材料あるいは目的に応じ、適宜、単
独又は2種以上を混合して用いる。Examples include ketones such as methyl ethyl ketone, esters such as ethyl acetate, etc. In the present invention, these organic solvents may be used alone or in a mixture of two or more depending on the materials used or the purpose. .
本発明に用いる噴射剤としては、液体プロパンガス、ジ
メチルエーテル、F−12(ジクロロジブロロメタン)
、F−22(モノクロロジフロロメタン)、F−14(
ジクロロテトラフロロエタン)、F−21(ジクロロモ
ノ70ロメタン)等があげられ、これらの単独、又は2
種以上を混合して用いる。Propellants used in the present invention include liquid propane gas, dimethyl ether, F-12 (dichlorodibroromethane)
, F-22 (monochlorodifluoromethane), F-14 (
(dichlorotetrafluoroethane), F-21 (dichloromono70lomethane), etc., and these alone or two
Use a mixture of more than one species.
本発明に用いる噴射剤は、本発明に用いるエチレン−酢
酸ビニル共重合体、粘着付与剤及び有機溶媒の混合溶液
25〜85重量パーセントに対して、噴射剤を75〜1
5重量パーセントの割合で用いるのが好ましい。The propellant used in the present invention is 75 to 1% by weight of the mixed solution of the ethylene-vinyl acetate copolymer, tackifier, and organic solvent used in the present invention.
Preferably, it is used in a proportion of 5% by weight.
本発明のエアゾル型スプレー接着剤は、用いるエチレン
−酢酸ビニル共重合体と粘着付与剤とを有機溶媒に所望
の割合で溶解し、この混合溶液を噴射剤と共に、通常の
方法によりエアゾル容器に充填して製造する。かくして
得られたエアゾル型スプレー接着剤は、その塗付に際し
ては、エアゾルスプレーパターン面積の広い、充分に霧
化されたエアゾルスプレー状態が得られ、接着剤被膜は
、エラストマー型接着剤のコンタクト性19四速する優
れたコンタクト性を示し、良好な接着性を有する。The aerosol type spray adhesive of the present invention is prepared by dissolving the ethylene-vinyl acetate copolymer and tackifier in an organic solvent in a desired ratio, and filling this mixed solution together with a propellant into an aerosol container by a conventional method. and manufacture it. When the aerosol spray adhesive thus obtained is applied, a sufficiently atomized aerosol spray state with a wide aerosol spray pattern area is obtained, and the adhesive film has a contact property 19 of the elastomer adhesive. It exhibits excellent contact properties with four speeds and has good adhesion.
本発明で得られるエアゾル型スプレー接着剤は、たとえ
ば紙、布、プラスチックフィルム、ガラスマット、カラ
スウール、写真、ボス、ター、金属箔、ウレタンフオー
ム、木材のごとき種々な材料の接着に用いることができ
る。又更にエアゾル型スプレー接着剤は塗付に際し、手
指に接着剤が付着することなしに、短時間に広い面積に
接着剤を均一に塗付することができ、容易にポスターや
前記被管材等を貼り合すことができる利点を有する。The aerosol spray adhesive obtained in the present invention can be used to bond various materials such as paper, cloth, plastic film, glass mat, glass wool, photographs, bosses, tars, metal foil, urethane foam, and wood. can. Furthermore, when applying an aerosol type spray adhesive, the adhesive can be applied uniformly over a wide area in a short time without getting the adhesive on your fingers, and it is easy to apply the adhesive to posters, the above-mentioned tube-covering materials, etc. It has the advantage of being able to be bonded.
以下実施例並びに比較例を示して本発明を具体的に説明
する。但し、これ等によって本発明を限定するものでは
ない。以下実施例中の部とあるのは、特に説明のない限
り重量部を示す。EXAMPLES The present invention will be specifically explained below with reference to Examples and Comparative Examples. However, the present invention is not limited to these. In the following examples, parts refer to parts by weight unless otherwise specified.
エアゾル型スプレー接着剤を表1に示す配合割合で、下
記の方法で調製した。An aerosol type spray adhesive was prepared in the following manner at the compounding ratio shown in Table 1.
トルエンにエチレン−酢酸ビニル共重合体と「エステル
ガムH」とを表1に示す割合でトルエンに溶解する。次
にエアゾル容器に通常の方法で上記混合溶液と噴射剤で
ある液体プロパンガスを表1の割合で充填した。Ethylene-vinyl acetate copolymer and "Ester Gum H" are dissolved in toluene in the proportions shown in Table 1. Next, the aerosol container was filled with the above mixed solution and liquid propane gas as a propellant in the proportions shown in Table 1 in a conventional manner.
(使用材料)
※i 商品名;rエバフレックス250 J(三井ポ
リケミカル■製)
※2 商品名;rエバフレックス15o」(三井ポリ
ケミカル■製)
X8 商品名;「エバフレックス40J(三井ポリケミ
カル■製〕
※4 商品名:[ソアレックス BHJ(日本合成化学
工業■製)
※5 商品名;[ソアレックス DHJ(日本合成化学
工業■製)
※6 商品名;[ソアレックス FHJ(日本合成化学
工業■製)
※7 水添ロジングリセリンエステル
(荒用化学■製)
かくして調製した各々の接着剤について、次の特性を測
定した。(Materials used) *i Product name; r Evaflex 250 J (Mitsui Polychemical ■) *2 Product name; r Evaflex 15o" (Mitsui Polychemical ■) X8 Product name; "Evaflex 40J (Mitsui Polychemical) *4 Product name: [Solex BHJ (manufactured by Nippon Gosei Chemical Co., Ltd.) *5 Product name; [Solex DHJ (manufactured by Nippon Gosei Chemical Co., Ltd.) *6 Product name; [Solex FHJ (manufactured by Nippon Gosei Chemical Co., Ltd.) (manufactured by Kogyo ■) *7 Hydrogenated rosin glycerin ester (manufactured by Arayo Kagaku ■) The following characteristics were measured for each of the adhesives thus prepared.
く溶媒への溶解性〉
エチレン−酢酸ビニル共重合体樹脂を粘着付与剤と共に
有機溶媒に溶解した時の状態を観察し、次の判定を行な
った。Solubility in Solvent> The state when the ethylene-vinyl acetate copolymer resin was dissolved in an organic solvent together with a tackifier was observed, and the following judgments were made.
判定基準
O;完全溶解
×一部分溶解又は不溶解
く噴霧性〉
各エアゾル型スプレー接着剤を、約20 cm離し、被
着材(Kライナー紙)に塗付する時のスプレー状態を観
察し、次の通り判定した。Judgment Criteria O; Completely dissolved x Partially dissolved or undissolved Sprayability> Observe the spray condition when each aerosol type spray adhesive is applied to the adherend (K liner paper) at a distance of approximately 20 cm, and then It was judged as follows.
判定基準
○;良好な霧化スプレー状態
×;霧化不可能
ぐ接着カン
各エアゾル型スプレー接着剤を、約20 cm離して、
1平方メートルあたり、被着材にライナー紙の場合は約
10of、被着材綿帆布の場合は約150yになるよう
にスプレー塗付する。塗付後10分間室温(20°C)
に放置し、指圧で貼り合わす。被着材の接着面積は、2
.5cm巾X6.Ocm、引張速度20 cm/分(島
津製作所■製オートグラフで測定する)で、接着7日目
に測定する。Judgment criteria ○; Good atomized spray condition ×; Non-atomizable Adhesive Can Place each aerosol type spray adhesive about 20 cm apart.
Spray the adhesive to the adherend in an amount of about 10 of if liner paper or about 150 y of cotton canvas to adhere to per square meter. Room temperature (20°C) for 10 minutes after application
Leave it on and stick it together using acupressure. The adhesive area of the adherend is 2
.. 5cm width x 6. Measurements are made on the 7th day of adhesion at a tensile speed of 20 cm/min (measured with an autograph manufactured by Shimadzu Corporation).
(単位; kf72.5 am巾) これらの判定結果を、表2に示す。(Unit: kf72.5 am width) The results of these determinations are shown in Table 2.
表 2
註 ※l: 溶解性不良のため、噴霧塗付性が悪く、接
着力試験ができなかった。Table 2 Notes *l: Due to poor solubility, spray applicability was poor and adhesion tests could not be conducted.
※2: 噴霧状態が悪く、かつコンタクト性が発現しな
かった。*2: The spray condition was poor and contact properties were not developed.
表2で明らかの如く、本発明の実施例1〜4のものは、
各試験でいづれも良好な結果を示した。As is clear from Table 2, Examples 1 to 4 of the present invention were
All tests showed good results.
しかるに、エチレン共重合量の70重量%より多い、比
較例1のものは、溶媒溶解性が悪く、噴霧状態も不良で
あった。However, in Comparative Example 1, in which the amount of ethylene copolymerized was more than 70% by weight, the solvent solubility was poor and the spray condition was also poor.
又、エチレン共重合量の20重量パーセントより少ない
比較例2は、噴霧状態が悪く、塗付被膜はコンタクト性
を示さず、接着力が無かった。In addition, in Comparative Example 2, in which the amount of ethylene copolymerized was less than 20% by weight, the spray condition was poor, and the applied film did not show contact properties and had no adhesive strength.
実施例5〜7
実施例1〜4と同様にして、有機溶媒、粘着付与剤、噴
霧剤の異なるものについて、表8に示す通りのエアゾル
型スプレー接着剤を調製し、各々実施例5〜7とした。Examples 5 to 7 In the same manner as Examples 1 to 4, aerosol type spray adhesives as shown in Table 8 were prepared using different organic solvents, tackifiers, and spray agents, and Examples 5 to 7 were prepared, respectively. And so.
表 8
(使用材料)
※8 ;商品名;ンアレツクスBH(日本合成化学工業
■製)
(酢酸ビニル共重合量55重
量パーセント)
※9 ;重合ロジン(パーキュレス■製)得られた実施
例5〜7のエアゾル型スプレー接着剤は、いづれも溶媒
溶解性、噴霧性、接着力が良好なものであった。Table 8 (Materials used) *8; Trade name; Narex BH (manufactured by Nippon Gosei Kagaku Kogyo ■) (vinyl acetate copolymerization amount: 55% by weight) *9; Polymerized rosin (manufactured by Percules ■) Examples 5 to 7 obtained All of the aerosol type spray adhesives had good solvent solubility, sprayability, and adhesive strength.
(以上)(that's all)
Claims (1)
酢酸ビニルとのエチレン−酢酸ビニル共重合体、粘着付
与剤、有機溶媒及び噴射剤を主成分とするエアゾル型ス
プレー接着剤。(2) An aerosol type spray adhesive whose main components are an ethylene-vinyl acetate copolymer of 20 to 70% by weight of ethylene and 80 to 80% by weight of vinyl acetate, a tackifier, an organic solvent, and a propellant.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4843083A JPS59172569A (en) | 1983-03-22 | 1983-03-22 | Aerosol type spraying adhesive |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4843083A JPS59172569A (en) | 1983-03-22 | 1983-03-22 | Aerosol type spraying adhesive |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59172569A true JPS59172569A (en) | 1984-09-29 |
JPH0332592B2 JPH0332592B2 (en) | 1991-05-13 |
Family
ID=12803128
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4843083A Granted JPS59172569A (en) | 1983-03-22 | 1983-03-22 | Aerosol type spraying adhesive |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59172569A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994006879A1 (en) * | 1992-09-14 | 1994-03-31 | Henkel Kommanditgesellschaft Auf Aktien | Anti-slip agent |
US5547712A (en) * | 1992-09-14 | 1996-08-20 | Henkel Kommanditgesellschaft Auf Aktien | Antislip preparation |
US5672199A (en) * | 1993-11-20 | 1997-09-30 | Henkel Kommanditgesellschaft Auf Aktien | Water-containing antislip composition |
JP2004083910A (en) * | 2002-08-22 | 2004-03-18 | Illinois Tool Works Inc <Itw> | Aerosol composition |
CN107286906A (en) * | 2017-08-10 | 2017-10-24 | 吴重慧 | A kind of formwork cloth spraying glue and preparation method |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56116766A (en) * | 1980-02-21 | 1981-09-12 | Sunstar Giken Kk | Foam adhesive and coating method thereof |
-
1983
- 1983-03-22 JP JP4843083A patent/JPS59172569A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56116766A (en) * | 1980-02-21 | 1981-09-12 | Sunstar Giken Kk | Foam adhesive and coating method thereof |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994006879A1 (en) * | 1992-09-14 | 1994-03-31 | Henkel Kommanditgesellschaft Auf Aktien | Anti-slip agent |
US5547712A (en) * | 1992-09-14 | 1996-08-20 | Henkel Kommanditgesellschaft Auf Aktien | Antislip preparation |
US5672199A (en) * | 1993-11-20 | 1997-09-30 | Henkel Kommanditgesellschaft Auf Aktien | Water-containing antislip composition |
JP2004083910A (en) * | 2002-08-22 | 2004-03-18 | Illinois Tool Works Inc <Itw> | Aerosol composition |
CN107286906A (en) * | 2017-08-10 | 2017-10-24 | 吴重慧 | A kind of formwork cloth spraying glue and preparation method |
Also Published As
Publication number | Publication date |
---|---|
JPH0332592B2 (en) | 1991-05-13 |
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