JPS63128089A - Alpha-cyanoacrylate adhesive composition - Google Patents
Alpha-cyanoacrylate adhesive compositionInfo
- Publication number
- JPS63128089A JPS63128089A JP27355386A JP27355386A JPS63128089A JP S63128089 A JPS63128089 A JP S63128089A JP 27355386 A JP27355386 A JP 27355386A JP 27355386 A JP27355386 A JP 27355386A JP S63128089 A JPS63128089 A JP S63128089A
- Authority
- JP
- Japan
- Prior art keywords
- cyanoacrylate
- weight
- adhesive composition
- parts
- added
- 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
- IJVRPNIWWODHHA-UHFFFAOYSA-N 2-cyanoprop-2-enoic acid Chemical compound OC(=O)C(=C)C#N IJVRPNIWWODHHA-UHFFFAOYSA-N 0.000 title claims abstract description 17
- 239000000203 mixture Substances 0.000 title claims abstract description 16
- 239000004830 Super Glue Substances 0.000 title claims description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 abstract description 20
- 239000000853 adhesive Substances 0.000 abstract description 19
- 229920001223 polyethylene glycol Polymers 0.000 abstract description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 4
- -1 acrylate compound Chemical class 0.000 abstract description 4
- 239000002202 Polyethylene glycol Substances 0.000 abstract description 3
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 abstract description 2
- 238000013329 compounding Methods 0.000 abstract 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- 229920001651 Cyanoacrylate Polymers 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- FGBJXOREULPLGL-UHFFFAOYSA-N ethyl cyanoacrylate Chemical compound CCOC(=O)C(=C)C#N FGBJXOREULPLGL-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 229920001342 Bakelite® Polymers 0.000 description 1
- 235000018185 Betula X alpestris Nutrition 0.000 description 1
- 235000018212 Betula X uliginosa Nutrition 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000008053 sultones Chemical class 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【発明の詳細な説明】
（産業上の利用分野）
本発明はα−シアノアクリレート系接着組成物に関する
もので、その目的は、初期接着強度の向上にある。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to an α-cyanoacrylate adhesive composition, and its purpose is to improve initial adhesive strength.
（従来の技術）
従来から接着組成物として使用されているα−Ｎ
■
シアノアクリレートは、一般式ＣＨ，＝ Ｃ−Ｃ００Ｒ
′ （式中、Ｒ′は炭素数１６以下のアルキル、アルケ
ニル、アラルキル、ハロアルキル、シクロヘキシル、フ
ェニル等を示す、）で示されるものであって、アニオン
重合を起し易く、固体表面に付着した水分や大気中の湿
度やその他アルカリ物質等の種々なアニオン活性物質に
よって触媒を用いることなく、常温において数秒〜数分
間の極く短時間で重合硬化する性質を有する。そのため
従来から瞬間接着剤として、工業用・医療用・一般家庭
用などに広く利用されている。(Prior art) α-N cyanoacrylate, which has been conventionally used as an adhesive composition, has the general formula CH,=C-C00R.
' (In the formula, R' represents alkyl, alkenyl, aralkyl, haloalkyl, cyclohexyl, phenyl, etc. having 16 or less carbon atoms), which easily undergoes anionic polymerization and is free from moisture adhering to the solid surface. It has the property of being polymerized and cured in a very short time of several seconds to several minutes at room temperature without using a catalyst by various anion active substances such as atmospheric humidity and other alkaline substances. Therefore, it has been widely used as an instant adhesive for industrial, medical, and general household purposes.
（発明が解決しようとする問題点）
しかし、このα−シアノアクリレート系接着剤において
は、被着体表面が酸性であったり、水分が少ないと、セ
ットタイムが著るしく遅くなるという欠点を有し、例え
ば木質材料、亜鉛クロメートメッキ鋼板、ポリエステル
、ベークライト、ＥＰＤＭなどを被着体とした場合には
、セットタイムが著るしく遅くなり、接着強度も低くな
るという問題があった。(Problems to be Solved by the Invention) However, this α-cyanoacrylate adhesive has the disadvantage that the set time is significantly slow if the surface of the adherend is acidic or has low moisture content. However, when the adherend is, for example, a wood material, a zinc chromate plated steel plate, polyester, Bakelite, EPDM, etc., there are problems in that the setting time is significantly slow and the adhesive strength is also low.
（問題点を解決するための手段）
本発明者等は、上記従来のα−シアノアクリレート系接
着剤のセットタイム等の改良のため鋭意研究を行なった
結果、α−シアノアクリレートにα−シアノアクリレー
トを共重合しうるアクリロキシ基又はメタアクリロキシ
基を有するポリエチレングリコール化合物を添加するこ
とにより、α−シアノアクリレートの特性を失なうこと
なく。(Means for Solving the Problems) As a result of intensive research to improve the setting time, etc. of the conventional α-cyanoacrylate adhesives, the present inventors found that α-cyanoacrylate By adding a polyethylene glycol compound having an acryloxy group or a methacryloxy group that can be copolymerized with α-cyanoacrylate, the properties of α-cyanoacrylate are not lost.
上記セットタイムの改良、接着強度の向上、保存安定性
の良好なものが得られることを見出し本発明を完成する
に至ったものである。The inventors have completed the present invention by discovering that the above-mentioned set time can be improved, adhesive strength can be improved, and storage stability can be improved.
すなわち、本発明のシアノアクリレートに添加する上記
反応性化合物は、次の一般式（１）で示（式中又は水素
原子又はメチル基であり、ｎは整数で４〜１００である
。）
なお、上記一般式（１）で示す反応性化合物としては１
例えば、テトラエチレングリコールジ（メタ）アクリレ
ート及びポリエチレングリコールジ（メタ）アクリレー
ト等があげられる。That is, the above-mentioned reactive compound added to the cyanoacrylate of the present invention is represented by the following general formula (1) (in the formula, it is a hydrogen atom or a methyl group, and n is an integer from 4 to 100.) The reactive compound represented by the above general formula (1) is 1
Examples include tetraethylene glycol di(meth)acrylate and polyethylene glycol di(meth)acrylate.
そして、これらの化合物の添加量は、α−シアノアクリ
レート１００重量部に対して０．０１〜１重量部の範囲
が特によく、この範囲を超えて多く添加すると反ってセ
ットタイムが遅くなり、粘度も高くなるので好ましくな
く、一方、ｏ、ｏｉ重量部未満では、その硬化促進が不
十分で、セットタイムの改良、および接着強度の改良等
に結がらないものとなる。又、上記一般式（１）中、整
数ｎが４未満のものはセットタイムの促進効果が乏しく
、一方、１００を超えるものは、α−シア、ノアクリレ
ートモノマーに対する溶解性が悪くなる欠点がある。The amount of these compounds to be added is particularly preferably in the range of 0.01 to 1 part by weight per 100 parts by weight of α-cyanoacrylate.If added in excess of this range, the setting time will be slow due to warping, and the viscosity will increase. On the other hand, if the amount is less than o or oi parts by weight, the curing acceleration will be insufficient and the setting time and adhesive strength will not be improved. In addition, in the above general formula (1), when the integer n is less than 4, the effect of accelerating the set time is poor, while when it exceeds 100, there is a drawback that the solubility in α-sia and noacrylate monomers becomes poor. .
次に上記本発明に係るα−シアノアクリレート接着剤組
成物に使用できる安定化剤としては、Ｓ０３、ＳＯ，、
パラトルエンスルホン酸、メタンスルホン酸、スルトン
、三フッ化ホウ素エーテル等が使用可能である０重合禁
止剤としてはハイドロキノン、ベンゾキノン、カテコー
ル、アルキルフェノール等がある。又、増粘剤としてポ
リマーやオリゴマー、例えばポリメチルメタクリレート
。Next, the stabilizers that can be used in the α-cyanoacrylate adhesive composition according to the present invention include S03, SO,
Para-toluenesulfonic acid, methanesulfonic acid, sultone, boron trifluoride ether, etc. can be used. Polymerization inhibitors that can be used include hydroquinone, benzoquinone, catechol, alkylphenol, and the like. Also, polymers and oligomers as thickeners, such as polymethyl methacrylate.
ポリ酢酸ビニル、ポリスチレン、ポリα−シアノアクリ
レート等の添加や微粉末シリカ等の無機増粘剤の添加も
可能である。さらに場合によっては。It is also possible to add polyvinyl acetate, polystyrene, polyα-cyanoacrylate, etc., and to add an inorganic thickener such as finely powdered silica. Even more in some cases.
α−シアノアクリレート組成物の物性を低下せしめるこ
とがなく、貯蔵安定性を損わない溶剤、可塑性、促進剤
、着色剤等の添加を行なうことも可能である。It is also possible to add solvents, plasticizers, accelerators, colorants, etc. that do not reduce the physical properties of the α-cyanoacrylate composition and do not impair storage stability.
（実施例） 実施例−１ α−シアノアクリレート１００重量部に対して。(Example) Example-1 Based on 100 parts by weight of α-cyanoacrylate.
安定化剤二三フッ化ホウ素ジエチルエーテル０゜００２
重量部、重合禁止剤：ハイドロキノン０゜０５重量部、
増粘剤：ポリメチルメタクリレート５重量部を添加して
接着剤組成物を作成し、この接着剤組成物に一般式（１
）の化合物（但しＸ＝ＣＨ，）をｎ÷４〜９０として各
々０．５重量部添加し、これを試料として反応性化合物
不在及びｎ＝１〜３の比較試料とともに、下記ＪＩＳに
基づいて試験を行なった。この結果を表１に示す。Stabilizer boron ditrifluoride diethyl ether 0°002
Parts by weight, polymerization inhibitor: 0.05 parts by weight of hydroquinone,
Thickener: 5 parts by weight of polymethyl methacrylate was added to prepare an adhesive composition, and the general formula (1) was added to this adhesive composition.
) compounds (where X=CH,) were added in an amount of 0.5 parts by weight each as n÷4 to 90, and these were used as samples along with comparative samples in which no reactive compound was present and n=1 to 3, based on the following JIS. I conducted a test. The results are shown in Table 1.
（以下余白）
〔備 考〕
１．セットタイム： ＪＩＳ Ｋ ６８６１ ｒα−シ
アノアクリレート系接着剤の試験方法」に準じた。(Margin below) [Notes] 1. Set time: According to JIS K 6861 "Test method for rα-cyanoacrylate adhesives".
２、引張剪断強度： ＪＩＳ Ｋ ６８６１ ｒα−シ
アノアクリレート系接着剤の試験方法」に準じた。2. Tensile shear strength: According to JIS K 6861 "Test method for rα-cyanoacrylate adhesives".
３、圧縮剪断強度： ＪＩＳ Ｋ ６８５２ ｒ接着剤
の圧縮剪断接着強さ試験方法」に準じた。3. Compressive shear strength: According to JIS K 6852 ``Test method for compressive shear adhesive strength of adhesives''.
４、貯蔵安定性 ： ＪＩＳ Ｋ ６８６１ ｒα−シ
アノアクリレート系接着剤の試験方法」に準じた。4. Storage stability: According to JIS K 6861 "Test method for rα-cyanoacrylate adhesives".
表１の結果からもわかるように、実施例−１の組成物、
すなわちα−エチルシアノアクリレートに上記一般式（
１）の化合物（Ｘ＝ＣＨ，、Ｙ＝ＣＭ３）を各々０．５
重量部添加した接着剤組成物は、被着体として鋼板、亜
鉛クロメートメッキ鋼板、カバ材を用いた場合、一般式
（１）の化合物を添加していないもの、もしくは添加し
ても、ｎ ＜ ４の比較例として示した試料に比し、そ
の硬化速度は著しく促進され、さらに引張剪断強度、圧
縮剪断強度とも明白に改善されており、特にこの特性は
、対象とする被着体によって差異がみられるものの上記
一般式（１）におけるｎ÷４〜９０の範囲内において全
体的な傾向として顕著に表われいる。As can be seen from the results in Table 1, the composition of Example-1,
That is, the above general formula (
1) Compounds (X=CH, Y=CM3) each at 0.5
When using a steel plate, a zinc chromate plated steel plate, or a birch material as an adherend, the adhesive composition to which the compound of general formula (1) is added is either not added, or even if it is added, n < Compared to the sample shown as a comparative example in No. 4, its curing speed was significantly accelerated, and its tensile shear strength and compressive shear strength were also clearly improved. However, the overall tendency is remarkable within the range of n÷4 to 90 in the above general formula (1).
実施例−２
α−エチレシアノアクリレート１００重量部に対して、
安定化剤：三フッ化ホウ素ジエチルエーテル０．００２
重量部、重合禁止剤：ハイドロキノン、０．０５重量部
、増粘剤：ポリメチルメタクリレート５重量部を添加し
て接着剤組成物を作成し、この接着剤組成物に一般式（
１）の化合物（但しＸ＝ＣＨ，、ｎ二２３）を添加しこ
れを試料として試験を行なった。Example-2 Based on 100 parts by weight of α-ethylecyanoacrylate,
Stabilizer: boron trifluoride diethyl ether 0.002
Parts by weight, polymerization inhibitor: hydroquinone, 0.05 parts by weight, thickener: 5 parts by weight of polymethyl methacrylate were added to prepare an adhesive composition.
The compound 1) (wherein X=CH, n223) was added and used as a sample for testing.
すなわち、この例では反応性化合物の添加量が諸特性に
及ぼす影響をテストしたもので、α−エチルシアノアク
リレート１００重量部に対して上記一般式（１）の化合
物（Ｘ＝ＣＨ３，ｎ÷２３）を０．０１〜１重量部添加
した試料を作成するとともに、この範囲外１例えばｏ、
ｏｏｓ重量部。That is, in this example, the effect of the amount of the reactive compound added on various properties was tested. ) is added to a sample containing 0.01 to 1 part by weight, and 1 part outside this range, such as o,
oos parts by weight.
５重量部を各々添加して作成した試料と、無添加の試料
とを比較例として作成し、これらの特性を調べたもので
ある。A sample prepared by adding 5 parts by weight of each and a sample without the additive were prepared as comparative examples, and their properties were investigated.
（以下余白）
表２の結果からも明らかなように、本発明の上記一般式
（１）で表わされる化合物をα−エチルシアノアクリレ
ートに添加したもの（実施例）は、その限定範囲におけ
る添加量に対応して比較例のものに比しセットタイムや
接着強度特性が優れていることがわかる。(Left below) As is clear from the results in Table 2, the compound represented by the above general formula (1) of the present invention is added to α-ethyl cyanoacrylate (Example) in an amount within the limited range. It can be seen that the set time and adhesive strength characteristics are superior to those of the comparative example.
一方、本発明の限定範囲を超える場合１例えば上記化合
物をα−エチルシアノアクリレート１００重量部に対し
５重量部添加したものは、その添加量に応じた特性の向
上はみられず１反って特性の低下とともに、該組成物自
体の粘度の上昇に伴って貯蔵安定性が悪くなる。On the other hand, when exceeding the limited range of the present invention 1 For example, when 5 parts by weight of the above compound is added to 100 parts by weight of α-ethyl cyanoacrylate, no improvement in properties is observed in accordance with the amount added, and 1 the properties are warped. As the viscosity of the composition itself decreases, the viscosity of the composition itself increases, resulting in poor storage stability.
又、上記一般式（１）の化合物を０．０１重量部未満、
すなわち、０．００５重量部或は無添加のものは１表示
したように硬化が遅延され、従ってセットタイムが著し
く長くなり、その接着強度も被着体によって若干差異は
あるものの全体的に低いものとなっている。In addition, less than 0.01 parts by weight of the compound of the above general formula (1),
In other words, with 0.005 parts by weight or with no additives, curing is delayed as shown in 1, so the set time is significantly longer, and the adhesive strength is generally lower, although it varies slightly depending on the adherend. It becomes.
（発明の効果）
以上のように本発明の接着剤組成物は、α−シアノアク
リレート１００重量部に対し上述した一般式（１）で示
される反応性化合物を０．０１〜１重量部添加してなる
ものであるので、従来のα−シアノアクリレート系接着
剤に比して、被着体に対するセットタイム、接着強度、
保存安定性等の特性を大幅に向上させるものとなる。(Effects of the Invention) As described above, the adhesive composition of the present invention can be obtained by adding 0.01 to 1 part by weight of the reactive compound represented by the above-mentioned general formula (1) to 100 parts by weight of α-cyanoacrylate. Compared to conventional α-cyanoacrylate adhesives, the set time for adherends, adhesive strength,
This greatly improves properties such as storage stability.
しかも上記反応性化合物の添加量を、その限定範囲内で
適宜変更することにより、被着体の性状等に対応させた
接着特性を発揮させ得ることができるので、その実使用
上の効果は顕著なものとなるのである。Moreover, by appropriately changing the amount of the above-mentioned reactive compound added within its limited range, it is possible to exhibit adhesive properties that correspond to the properties of the adherend, so the effect in practical use is remarkable. It becomes something.
一以上一one or more one
Claims (1)
で示される反応性化合物を０．０１〜１重量部添加して
なるα−シアノアクリレート接着剤組成物。 一般式（１） ▲数式、化学式、表等があります▼ 〔式中Ｘは水素原子又はメチル基であり、ｎは整数で４
〜１００である。〕[Claims] To 100 parts by weight of α-cyanoacrylate, the general formula (1) is added.
An α-cyanoacrylate adhesive composition containing 0.01 to 1 part by weight of a reactive compound represented by: General formula (1) ▲There are mathematical formulas, chemical formulas, tables, etc.▼ [In the formula, X is a hydrogen atom or a methyl group, and n is an integer of 4
~100. ]
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27355386A JPS63128089A (en) | 1986-11-17 | 1986-11-17 | Alpha-cyanoacrylate adhesive composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27355386A JPS63128089A (en) | 1986-11-17 | 1986-11-17 | Alpha-cyanoacrylate adhesive composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS63128089A true JPS63128089A (en) | 1988-05-31 |
Family
ID=17529414
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP27355386A Pending JPS63128089A (en) | 1986-11-17 | 1986-11-17 | Alpha-cyanoacrylate adhesive composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63128089A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04159382A (en) * | 1990-10-22 | 1992-06-02 | Sekisui Aikoo Kk | Alpha-cyanoacrylate-based adhesive composition |
| WO1994011454A1 (en) * | 1992-11-09 | 1994-05-26 | Toagosei Chemical Industry Co., Ltd. | Cyanoacrylate adhesive composition |
| WO2002009784A1 (en) * | 2000-08-02 | 2002-02-07 | Universidad De Alicante | Acrylic-based adhesive composition |
| EP2508543A1 (en) * | 2011-04-04 | 2012-10-10 | Bioadhesives Medtech Solutions, S.L. | Novel adhesive compositions and uses thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5695966A (en) * | 1979-12-28 | 1981-08-03 | Matsumoto Seiyaku Kogyo Kk | Two-pack composition and adhesive bonding therewith |
-
1986
- 1986-11-17 JP JP27355386A patent/JPS63128089A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5695966A (en) * | 1979-12-28 | 1981-08-03 | Matsumoto Seiyaku Kogyo Kk | Two-pack composition and adhesive bonding therewith |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04159382A (en) * | 1990-10-22 | 1992-06-02 | Sekisui Aikoo Kk | Alpha-cyanoacrylate-based adhesive composition |
| WO1994011454A1 (en) * | 1992-11-09 | 1994-05-26 | Toagosei Chemical Industry Co., Ltd. | Cyanoacrylate adhesive composition |
| US5536799A (en) * | 1992-11-09 | 1996-07-16 | Toagosei Co., Ltd. | Cyanocrylate adhesive composition |
| WO2002009784A1 (en) * | 2000-08-02 | 2002-02-07 | Universidad De Alicante | Acrylic-based adhesive composition |
| EP2508543A1 (en) * | 2011-04-04 | 2012-10-10 | Bioadhesives Medtech Solutions, S.L. | Novel adhesive compositions and uses thereof |
| WO2012136639A1 (en) * | 2011-04-04 | 2012-10-11 | Bioadhesives Medtech Solutions, S.L. | Novel adhesive compositions and uses thereof |
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