JPS5984961A - Adhesive - Google Patents

Adhesive

Info

Publication number
JPS5984961A
JPS5984961A JP19337582A JP19337582A JPS5984961A JP S5984961 A JPS5984961 A JP S5984961A JP 19337582 A JP19337582 A JP 19337582A JP 19337582 A JP19337582 A JP 19337582A JP S5984961 A JPS5984961 A JP S5984961A
Authority
JP
Japan
Prior art keywords
adhesive
resin
hollow particles
strength
micro hollow
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
Application number
JP19337582A
Other languages
Japanese (ja)
Inventor
Takashi Fujii
貴 藤井
Masaru Fukushima
優 福島
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.)
AGC Inc
Original Assignee
Asahi Glass 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 Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP19337582A priority Critical patent/JPS5984961A/en
Publication of JPS5984961A publication Critical patent/JPS5984961A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide an adhesive having high adhesive strength and applicable even to a vertical wall without sagging, by adding tiny hollow particles to an adhesive. CONSTITUTION:The objective adhesive is prepared by adding preferably 5-70% of tiny hollow particles (preferably silica balloon having average particle diameter of 5-200mu) to an adhesive based on e.g. epoxy resin, urea resin, melamine resin, phenolic resin, vinyl acetate resin, acrylic emulsion, hot-melt, natural rubber, chloroprene, SBR, etc.

Description

【発明の詳細な説明】 本発明は接着剤、特に接着強度の高い接層剤に係るもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to adhesives, particularly adhesives with high adhesive strength.

近年高分子化学の著しい発達に伴ない、同種のみならず
互に異種の利料奮容易且強力に接着し得る各種の接着剤
が開発されている。
In recent years, with the remarkable development of polymer chemistry, various adhesives have been developed that can easily and strongly bond not only the same type of adhesive but also different types of adhesives to each other.

これら接着剤の大部分は、有機系高分子材料から成り、
接着剤層の厚みは最大強度を発揮させる為には厚くとも
100μ程度であり、接着強度の発現は接着剤層と被接
着材料との界面で行なわれていた。
Most of these adhesives are made of organic polymer materials,
The thickness of the adhesive layer is approximately 100 microns at most in order to exhibit maximum strength, and the adhesive strength is developed at the interface between the adhesive layer and the material to be adhered.

これは、接着剤の材料である有機系高分子材料そのもの
が一般的にそれ程強度の高いものでなく、例えばニトリ
ルゴムの様なゴム系の接着剤に見られるように、接着剤
Niをあまり厚くすると接着剤そのものが有するゴム様
弾性が生じ、強い力に対し7、接着剤層自体の引き裂き
現象が生ずることに代表される。
This is because the organic polymer material itself that is the material of the adhesive is generally not very strong, and for example, as seen in rubber adhesives such as nitrile rubber, the Ni adhesive is not thick enough. Then, the adhesive itself exhibits rubber-like elasticity, which is typified by the tearing phenomenon of the adhesive layer itself in response to strong force.

一方、これら有機系高分子材料から成る接’X4剤中に
炭カル等の添加剤を加えたものも知られている。しかし
ながら接着剤は、大部分が増量剤や接着剤が硬化した際
見られる所謂ヤセ現象と言われる体積収縮全防止する役
割は有しているものの、接着剤としての接着強度の向上
には実質的に関与しでいないのみならず、接着剤の見掛
は比重が上り、垂直面に適用した際にタレ現象音生じた
り、又粘度が著しく増大して塗布が困難になる等の欠点
を有している。
On the other hand, it is also known that additives such as charcoal are added to the adhesive X4 made of these organic polymeric materials. However, although most adhesives have the role of completely preventing volume shrinkage, the so-called fading phenomenon that occurs when fillers and adhesives harden, they do not substantially improve the adhesive strength of adhesives. Not only does it not play a role in this, but it also has disadvantages such as the apparent specific gravity of the adhesive, which causes sagging noise when applied to a vertical surface, and a marked increase in viscosity, making it difficult to apply. ing.

本発明者は、これら従来の接着剤が有していた諸欠点會
解消することを目的として種々研究。
The present inventor has conducted various studies with the aim of solving the various drawbacks that these conventional adhesives had.

検討した処、接着剤1−自体全強化出来るならば、特に
新らたに接着剤そのものの組成音度えなくても、従来そ
の接着剤が有していた接着強度をほぼ倍増或はそれ以上
にせしめることが出来ること?見出した。かくして本発
明は、接着剤中に微小中空粒体な混入せしめて成る接着
剤全提供するにある。
After some consideration, we found that if adhesive 1 itself could be fully strengthened, it would be possible to almost double or even exceed the adhesive strength that conventional adhesives had, without having to change the composition of the adhesive itself. Is it possible to make it false? I found it. Thus, the present invention provides an entire adhesive comprising fine hollow particles mixed into the adhesive.

本発明において微小中空球全混入せしめられた接着剤は
、−見多数の泡を有するように見え、これが強度?増大
することは意外であるが、容量当りの接着剤樹脂の量を
減じて低収縮性にすることが出来、内部応力が減じられ
ることにより強度の増大が計れるものと思われる。
In the present invention, the adhesive completely mixed with microscopic hollow spheres appears to have a large number of bubbles, which indicates its strength. Although this increase is surprising, it is believed that the amount of adhesive resin per volume can be reduced to provide lower shrinkage, and the internal stress can be reduced, thereby increasing the strength.

本発明に用いられる接着剤としては、例えばエポキシ樹
脂系、エリア樹脂系、メラミン樹脂系、フェノール樹脂
系、酢酸ビニル樹脂系、アクリルエマルジョン系、ホッ
トメルトl 天然コム系、クロロプレン系、SBR系等
全適宜採用することが出来る。
Adhesives used in the present invention include, for example, epoxy resin, area resin, melamine resin, phenol resin, vinyl acetate resin, acrylic emulsion, hot melt, natural comb, chloroprene, SBR, etc. It can be adopted as appropriate.

又、微小中空粒体としては、適宜な材質を用い得るが、
接着剤と相互に反応し、接着効果や接着剤自身の有効な
性質全阻害するものであっテハ々らず、この為一般に無
機質が好ましい。
In addition, as the micro hollow particles, an appropriate material can be used, but
Inorganic materials are generally preferred because they do not interact with the adhesive and interfere with the adhesive effect or the effective properties of the adhesive itself.

更に、この様な無機質であっても、それが一旦溶融する
等して所謂ガラス質になったものよりも、これら無機質
材料が加熱乾燥されたガラス化していない穀?有する微
小中空体である方が本発明に用いるのに適している。
Furthermore, even if such inorganic materials are used, grains that have not been vitrified by heating and drying are better than those that have become so-called glass by being melted. Microhollow bodies having the same structure are more suitable for use in the present invention.

かかる理由は必ずしも明確ではないが、接着剤自身が中
空体の穀に一部浸透して同化することにより、接着剤と
中空体とが十分に一体化され、(−かも中空体の穀自身
も強度が増加し、全体的に接着剤層の強度が効果的に増
強される為と思われる。
The reason for this is not necessarily clear, but the adhesive itself partially penetrates and assimilates into the grain of the hollow body, so that the adhesive and the hollow body are sufficiently integrated (-and the grain of the hollow body itself also). This seems to be because the strength is increased and the overall strength of the adhesive layer is effectively enhanced.

かかる中空体を構成する無機質としては、例えばシリカ
、珪酸ンーダ、硼珪酸ガラス、アルミナ、シリカ−アル
ミナ等を適宜採用し得るが、これらのうちシリカ質の中
空体は特に高い補強効果が得られるので好ましい。
As the inorganic material constituting such a hollow body, for example, silica, silicate powder, borosilicate glass, alumina, silica-alumina, etc. can be appropriately adopted, but among these, a siliceous hollow body has a particularly high reinforcing effect. preferable.

又微小中空体の平均粒径は、一般に5〜200μ程度7
c採用するのが好ましく、上記範囲を逸脱する場合−は
、効果的な補強効果が得られなくなる虞れがあるので好
ましくない。
In addition, the average particle size of the micro hollow bodies is generally about 5 to 200μ7.
It is preferable to adopt C. If it deviates from the above range, it is not preferable because there is a risk that an effective reinforcing effect cannot be obtained.

接着剤とこれら微小中空体との混合割合は、一般に後者
が5〜70容−i%であるのが適尚である。
It is generally appropriate that the mixing ratio of the adhesive and these micro hollow bodies is 5 to 70 volume-i% of the latter.

混合割合が上記範囲を逸脱する場合には、効果的な補強
効果が得られなかったり、接着効果全阻害したりする虞
れがあるので何れも好ましくない。
If the mixing ratio deviates from the above range, there is a risk that an effective reinforcing effect may not be obtained or that the adhesive effect may be completely inhibited, which is not preferable.

尚、本発明に用いられる微小中空体の製造法に特に制限
はなく、例えばシリカ系の微小中空体を例に採ると、ナ
トリウムシリケートと発泡剤と全混合した水溶液を用い
、これ奮スフ“レードライヤーにかけて微小中空体とし
、更に必要に応じ加熱する等の手段により得ることが出
来る0 次に本発明全実施例により説明する。
Note that there are no particular limitations on the method for producing the micro hollow bodies used in the present invention. For example, taking silica-based micro hollow bodies as an example, an aqueous solution containing sodium silicate and a blowing agent is used, This can be obtained by applying a dryer to form micro hollow bodies and further heating if necessary.Next, all embodiments of the present invention will be explained.

実施例1 エポキシ樹脂系接着剤(方メダイン社製商品名エポキシ
$1500)10 F、硬化剤10Fに対し、平均−粒
径65μのシリカッくル−フCPQ、社製商品名Q−セ
ル)4f金十分混合し7て比、Qf、 0.58の接着
剤組成物を得た。かかる接着前+1 ’に接着面積6.
2 +) C,J 2.(有する鉄製被接着体に厚さ4
00μに塗布し1、同様な被接着体との接着k R’1
つだ。
Example 1 Epoxy resin adhesive (manufactured by Homedain Co., Ltd., trade name: Epoxy $1500) 10 F, curing agent: 10 F, average particle size of 65 μm, silica roof CPQ, trade name (Q-Cell, made by Co., Ltd.) 4 f The gold was thoroughly mixed to obtain an adhesive composition having a Qf of 0.58. Adhesion area 6. +1' before such adhesion.
2 +) C, J 2. (The thickness of the iron adherend is 4
00μ 1, adhesion to similar adherend k R'1
Tsuda.

このとき室温10時間の条件下に接着剤を乾燥固化せし
めた。
At this time, the adhesive was dried and solidified at room temperature for 10 hours.

かくして得られた接着体の接着強度は、J工S−1c6
850及びJより −K 5854による接オを強度の
測定法によって引張り剪断力、剥離、引き離し強度を測
定した処、引張り剪断力ij: 120Ay/l:dl
 s  引き離し力は1t、z5kg/cJ、剥離ゆ5
L5にグとなった。
The adhesive strength of the thus obtained adhesive was J Engineering S-1c6.
From 850 and J-K 5854, the tensile shear force, peeling, and peeling strength were measured using the strength measurement method, and the tensile shear force ij: 120Ay/l:dl
s Peeling force is 1t, z5kg/cJ, peeling force 5
It turned into L5.

尚、比較の為、シリカバルーン全添加しない外は上記実
施例と同様に接着せしめた接着体の引張り剪断力、引き
離し、剥離強度は夫々60#/cfl+  7.5 h
lct4. 35 kであり、本発明の接着剤の強度よ
りかなり低いことが理解される。
For comparison, the tensile shear force, peel strength, and peel strength of the bonded body bonded in the same manner as in the above example except that no silica balloon was added were 60 #/cfl+7.5 h.
lct4. 35 k, which is understood to be significantly lower than the strength of the adhesive of the present invention.

実施例2 エポキシ樹脂系接着剤(セメダイン社製、商品名工ホキ
シナ1500 ) 10 f、  硬化剤102に対し
、平均粒径75μのシリカバルー729全土分混合して
比重0.76の接着剤組成物を得た。これを実施例1の
ごとく塗布し、接着強度を測定した処、引張り剪断力は
90 h/lri 、引き離し力は9h/d、剥離は7
0却であった。
Example 2 An adhesive composition with a specific gravity of 0.76 was obtained by mixing 10 f of an epoxy resin adhesive (manufactured by Cemedine Co., Ltd., trade name Ko Hoxina 1500) and 102 of a curing agent with the entirety of Silica Balu 729 with an average particle size of 75 μm. Ta. This was applied as in Example 1 and the adhesive strength was measured. The tensile shearing force was 90 h/lri, the peeling force was 9 h/d, and the peeling was 7.
It was a zero rejection.

尚、シリカバルー/を添加しない場合の強度は、引張り
剪断力6o hAvl 、  引き離し力は7、5 h
/d、剥離は35にりであり、 本発明の接着強度の向
上が理解できる。
In addition, the strength when silica ball is not added is tensile shearing force of 6 ohAvl and peeling force of 7.5 h.
/d, and the peeling was 35 glue, which shows the improvement in adhesive strength of the present invention.

実施例3 エポキシアクリレート系接着剤(昭和高分子社製、商品
名デボキシ802)100部、硬化剤(日本油脂製、商
品名パーメック)1部、促進剤(ナフテノ酸コパル) 
) 0.5部に対し、平均粒径65μのシリカバルーン
(PQ、社製、商品名Q、−セル920部を十分混合し
て接着剤組成物を得た。実施例1のごとく塗布し、40
℃。
Example 3 100 parts of epoxy acrylate adhesive (manufactured by Showa Kobunshi Co., Ltd., trade name: DEBOXY 802), 1 part of curing agent (manufactured by NOF Corporation, trade name: Permec), accelerator (copal naphthenoate)
) and 920 parts of silica balloons with an average particle size of 65 μm (PQ, manufactured by Co., Ltd., trade name Q, -cell) were sufficiently mixed to obtain an adhesive composition. Coated as in Example 1, 40
℃.

8時間の条件下に接着剤全乾燥固化せしめた。The adhesive was completely dried and solidified for 8 hours.

実施例1のごとく強度を測定した処、引張り剪断力は8
0Av/d、引き離し強さ16: 5 h/ caとな
った。
When the strength was measured as in Example 1, the tensile shear force was 8
0 Av/d, and the peeling strength was 16:5 h/ca.

比較の為、シリカバルーンを添加しない外は同条件で接
着せしめた接着体の引張り剪断力は35 h/crll
 1引き離し強さは9 ky/ cJであり、本発明の
効果が理解される。
For comparison, the tensile shearing force of an adhesive bonded under the same conditions except without the addition of silica balloons was 35 h/crll.
The 1-pull-off strength was 9 ky/cJ, and the effect of the present invention can be understood.

Claims (1)

【特許請求の範囲】 1、 微小中空粒体を混入してなる接着剤。 2、 微小中空粒体は、平均粒径5〜200μである請
求の範囲(1)の接着剤。 3、 微小中空粒体は、無機質である請求の範囲(1)
又は(2)の接着剤。 4、 微小中空粒体は、シリカバルーンである請求の範
囲(1)又は(2)の接着剤。 5、 微小中空粒体の混入量は、5〜70容量裂である
請求の範囲(1)の接着剤。 6、 接:着剤はその組成がエポキシ樹脂系、ユリア樹
脂系、メラミン樹脂系、フェノール樹脂系、酢酸ビニル
樹脂系、アクリルエマルジョノ、ホットメルト、天然ゴ
ム系、クロロプレ/系、  SBR系である請求の範囲
(1)の接着剤。
[Claims] 1. An adhesive containing microscopic hollow particles. 2. The adhesive according to claim (1), wherein the micro hollow particles have an average particle size of 5 to 200μ. 3. Claim (1) that the micro hollow particles are inorganic.
Or (2) adhesive. 4. The adhesive according to claim (1) or (2), wherein the micro hollow particles are silica balloons. 5. The adhesive according to claim 1, wherein the amount of the micro hollow particles mixed is 5 to 70 volumes. 6. Adhesive: The composition of the adhesive is epoxy resin, urea resin, melamine resin, phenol resin, vinyl acetate resin, acrylic emulsion, hot melt, natural rubber, chloropre/SBR, or SBR. Adhesive according to claim (1).
JP19337582A 1982-11-05 1982-11-05 Adhesive Pending JPS5984961A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19337582A JPS5984961A (en) 1982-11-05 1982-11-05 Adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19337582A JPS5984961A (en) 1982-11-05 1982-11-05 Adhesive

Publications (1)

Publication Number Publication Date
JPS5984961A true JPS5984961A (en) 1984-05-16

Family

ID=16306869

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19337582A Pending JPS5984961A (en) 1982-11-05 1982-11-05 Adhesive

Country Status (1)

Country Link
JP (1) JPS5984961A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6389582A (en) * 1986-10-02 1988-04-20 Sekisui Chem Co Ltd Foam-containing tacky-adhesive or adhesive
JPS63146973A (en) * 1986-12-11 1988-06-18 Canon Inc Adhesive
JPH02158676A (en) * 1988-12-10 1990-06-19 Daiabondo Kogyo Kk Adhesive for assembling speaker
JPH02286769A (en) * 1989-04-28 1990-11-26 Canon Inc Adhesive
EP0792926A2 (en) * 1996-02-28 1997-09-03 Henkel Kommanditgesellschaft auf Aktien Aqueous dispersion adhesive

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5589373A (en) * 1978-12-27 1980-07-05 Nippon Gakki Seizo Kk Composition for low-pressure bonding

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5589373A (en) * 1978-12-27 1980-07-05 Nippon Gakki Seizo Kk Composition for low-pressure bonding

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6389582A (en) * 1986-10-02 1988-04-20 Sekisui Chem Co Ltd Foam-containing tacky-adhesive or adhesive
JPS63146973A (en) * 1986-12-11 1988-06-18 Canon Inc Adhesive
JPH02158676A (en) * 1988-12-10 1990-06-19 Daiabondo Kogyo Kk Adhesive for assembling speaker
JPH02286769A (en) * 1989-04-28 1990-11-26 Canon Inc Adhesive
EP0792926A2 (en) * 1996-02-28 1997-09-03 Henkel Kommanditgesellschaft auf Aktien Aqueous dispersion adhesive
EP0792926A3 (en) * 1996-02-28 1999-12-22 Henkel Kommanditgesellschaft auf Aktien Aqueous dispersion adhesive

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