JPS58179279A - Corrosion protecting adhesive - Google Patents

Corrosion protecting adhesive

Info

Publication number
JPS58179279A
JPS58179279A JP6308082A JP6308082A JPS58179279A JP S58179279 A JPS58179279 A JP S58179279A JP 6308082 A JP6308082 A JP 6308082A JP 6308082 A JP6308082 A JP 6308082A JP S58179279 A JPS58179279 A JP S58179279A
Authority
JP
Japan
Prior art keywords
adhesive
powder
metallic
rust
gold
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
JP6308082A
Other languages
Japanese (ja)
Inventor
Shinichi Satsumoto
札本 進一
Takeshi Murakami
武 村上
Hidenori Idate
井立 秀則
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.)
Panasonic Electric Works Co Ltd
Original Assignee
Matsushita Electric Works 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 Matsushita Electric Works Ltd filed Critical Matsushita Electric Works Ltd
Priority to JP6308082A priority Critical patent/JPS58179279A/en
Publication of JPS58179279A publication Critical patent/JPS58179279A/en
Pending legal-status Critical Current

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  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE:To provide a corrosion protecting adhesive exhibiting sufficiently high corrosion protecting effect without lowering the adhesive strength, by compounding a corrosion protecting agent comprising metallic power having larger ionization tendency than the metallic component of the metallic material to be bonded. CONSTITUTION:The objective corrosion protection adhesive is prepared by compounding an adhesive (e.g. bisphenol-type epoxy resin, resol-type phenolic resin, novolac-type phenolic resin, butyral resin, etc.) with a corrosion protecting agent comprising metallic powder (e.g. Al, Zn, Mn, Cr, Mo, Ti, etc. preferably having a particle diameter of 2-6mu) having larger ionization tendency than the metallic component of the metallic material to be bonded. The amount of the metallic powder is 5-20 times the weight of the base adhesive. The metallic powder is preferably flaky Zn powder having a thickness of 1.5-2mu and a diameter of 6-12mu.

Description

【発明の詳細な説明】 この発明は防錆接層剤に関するものである。[Detailed description of the invention] This invention relates to a rust-preventing adhesive.

一般に、銅板等の金−材料を接層剤によって接層する場
合には、接層すべき部分をサンドペーパー等を用いて粗
面化し、そこへ接着剤を塗布して接層することが付われ
ている。この場合、粗面化された金−材料の部分は錆び
やすいため、接着剤を逼って空気や水が租rkiK達し
ないように、接着剤の七に防錆塗料を塗布すること等が
行われる。
Generally, when bonding gold materials such as copper plates with a bonding agent, it is necessary to roughen the surface of the area to be bonded using sandpaper, etc., and then apply the bonding agent there. It is being said. In this case, since the roughened gold material part is prone to rust, it is necessary to apply anti-rust paint to the surface of the adhesive to prevent air and water from reaching the surface of the adhesive. be exposed.

しかしながら、接着された金属材料の接着剤部分に防錆
塗料を完全番こ塗布することは、接着剤の存在する部分
が金属材料と金属材料との間であって空隙が小さいため
殆ど不可能である。したがって、接着剤部分から発錆す
るという現象が生じていた。
However, it is almost impossible to completely coat the adhesive part of the bonded metal materials with anti-rust paint because the part where the adhesive exists is between the metal materials and the gap is small. be. Therefore, a phenomenon occurred in which rust developed from the adhesive portion.

そこで、発明者らは、接着剤自身に防錆力を保持させる
ことができないかと研究を1ねたのであるが、IjI:
着剤に防錆剤を配合すると、今度は接着剤の接着力が著
しく低下するという問題に当面した。この問題を解決す
べくさらに研究を1ねた結果、接層剤に、接合すべき金
属材料中の金属成分よりもイオン化傾向の大な金属の粉
末を含有させると、接着剤の接着力をあまり低下させる
ことなく充分な防錆効果が得られるようになることを見
いだし、この発明に到達した。
Therefore, the inventors conducted research to see if it was possible to make the adhesive itself retain its anti-rust properties, and found that IjI:
We encountered the problem that when a rust preventive agent was added to an adhesive, the adhesive strength of the adhesive was significantly reduced. As a result of further research to solve this problem, we found that if the adhesive contains a metal powder that has a higher ionization tendency than the metal components in the metal materials to be bonded, the adhesive force of the adhesive will be significantly reduced. It was discovered that a sufficient rust prevention effect can be obtained without deterioration, and the present invention was achieved.

すなわち、この発明は、接合すべき金属材料中の金属成
分よりもイオン化傾向の大な金−の粉末が防錆剤として
配合されている防錆接着剤をその賛旨とするものである
That is, the gist of the present invention is a rust-preventing adhesive containing gold powder, which has a greater tendency to ionize than the metal components in the metal materials to be joined, as a rust preventive agent.

つき゛に、この発明について評しく説明する、接合すべ
き金員材料としては、鉄、ステンレス。
In this regard, the metal materials to be joined will be iron and stainless steel.

鋼、鉛吟からなるものがあけられ、材料の形状は何ら限
定するものではない。板状であってもよく、パイプ状で
あってもよい。
It can be made of steel or lead metal, and the shape of the material is not limited in any way. It may be plate-shaped or pipe-shaped.

接台すべき金−材料の金−成分Jりもイオン化傾向の大
な金−の粉末は、接合すべき金−材料の金−成分に応じ
て上記に列記する金員の粉末の−なかから遺はれる、A
I 、 Zn 、 Mn 、 Cr 、 Mo 、 ”
l’i等の粉末。このような金−粉末は、微粉末状がよ
く、その粒径が2〜6μのものが好ましい。最も好まし
いのは3〜4μのものである。粒径が2μよりも小さい
ものは、後記の接層剤(主剤)に分散させるときに単粒
子状に分散せず粒子同志の皺果のためによい接層剤塗膜
が得られないし、防錆効果もあまり発揮されなくなる。
The gold powder to be bonded has a high ionization tendency, depending on the gold component of the material to be bonded, from among the metal powders listed above according to the gold component of the material to be bonded. Legacy, A
I, Zn, Mn, Cr, Mo,”
The powder of l'i et al. Such gold powder is preferably in the form of a fine powder, and preferably has a particle size of 2 to 6 microns. The most preferable one is 3 to 4μ. If the particle size is smaller than 2μ, it will not be dispersed into single particles when dispersed in the adhesive agent (main agent) described later, and a good adhesive coating will not be obtained due to wrinkles between the particles. The rust effect will also be less effective.

また、粒径が6μよりも大きくなると粒子が接層剤から
分離しやすくなり、接着強度が低くなる傾向がみられる
からである。1 このような金員粉末の配合緻は、金員粉末がl蓋基準で
接着剤(主剤)の5〜20倍になるように設定すること
が好ましい。最も好ましいのは10〜15倍である。配
合菫が5倍未満では導電性が発生せずガルバニックな防
錆効果が期待できず、また20倍を超えると接層剤の接
着力が大きく低重する傾向がみられるからである。
Further, if the particle size is larger than 6 μm, the particles tend to separate from the adhesive, and the adhesive strength tends to decrease. 1. It is preferable to set the compounding ratio of the metal powder such that the metal powder is 5 to 20 times the amount of the adhesive (main ingredient) based on one lid. The most preferred is 10 to 15 times. If the violet content is less than 5 times, conductivity will not occur and no galvanic rust prevention effect can be expected, and if it exceeds 20 times, the adhesive strength of the adhesive will tend to be large and the weight will be low.

的記金属粉末のなかでも、特にZn粉末は、接合すべき
金−材料の種類を問わず用いることができ、その防錆効
果も顕著である。Zn粉末は、粒状であっても充分な防
錆効果を発揮するが、最も好ましいのは鱗片状のもので
ある。鱗片状のものは、厚みが1.5〜2μで、直性が
6〜12μのものが特に効果の点で好ましい。
Among the metal powders, Zn powder in particular can be used regardless of the type of gold material to be joined, and its rust-preventing effect is also remarkable. Zn powder exhibits a sufficient rust-preventing effect even when it is in the form of particles, but the most preferable one is in the form of scales. The scale-like material preferably has a thickness of 1.5 to 2 .mu.m and a straightness of 6 to 12 .mu.m, particularly from the viewpoint of effectiveness.

上記金員粉末が配合きれる接着剤(主剤)は、接合すべ
き金−材料に対する接着能を有していれはよく、その種
類を限定するものではない。しかしながら、金−粉末を
配合しても接着力の低下が少ない等の見地から、つぎの
ような樹脂が接着剤として用いられる。ビスフェノール
タイプのエポキシ樹脂、レゾールタイプの7エノール樹
脂、ノボラックタイプの7エノール樹脂、ブチラール樹
脂、アクリル樹脂2反応性塩化ビニル樹脂(例えは、塩
化ビニルと酢酸ビニルとの共1合体であって比較的低電
今度のものにカルボキシル基を導入したもの)、ウレタ
ン系樹脂。なお、鋼板を塩化ビニル樹脂、特に無gJ塑
の硬質塩化ビニル樹脂で被櫃して雨樋等の製品をつくる
場合には、接着剤樹脂として、変性アクリル樹脂(分子
内に酸基。
The adhesive (main agent) to which the above-mentioned metal powder can be mixed may be any adhesive having adhesive ability to the gold-materials to be bonded, and the type thereof is not limited. However, the following resins are used as adhesives from the viewpoint that the adhesion strength does not decrease much even when gold powder is mixed therein. Bisphenol-type epoxy resin, resol-type 7-enol resin, novolac-type 7-enol resin, butyral resin, acrylic resin, di-reactive vinyl chloride resin (for example, a comonomer of vinyl chloride and vinyl acetate, and relatively Low-voltage products with carboxyl groups introduced), urethane resins. In addition, when manufacturing products such as rain gutters by covering steel sheets with vinyl chloride resin, especially non-gJ plastic hard vinyl chloride resin, modified acrylic resin (with acid groups in the molecule) is used as the adhesive resin.

水酸基、アミド基、アミド・メチロール基、エポキシ基
、ヒドロキシル基等の反応性官能基を含むメチルメタア
クリレート七ツマ−をメチルメタアクリレート1モルに
対して1150〜l/100モルの割合で配合し共厘合
させたもの)を用いることが好ましい。この樹脂は、鋼
板と塩化ビニル樹脂の双方に対する接着力に富んでいる
のである。
Methyl methacrylate 7mer containing reactive functional groups such as hydroxyl group, amide group, amide/methylol group, epoxy group, hydroxyl group, etc. is blended at a ratio of 1150 to 1/100 mol to 1 mol of methyl methacrylate. It is preferable to use a combination of the two. This resin has excellent adhesion to both steel plates and vinyl chloride resin.

この発明の防錆接着剤は、上記の樹脂に前記の金−粉末
を配合し、さらに必要に応じて、硬化促進制9分散・沈
降防止剤等を配合することにより製造される。なお、A
il記金楓粉末率体でなく、その金−粉末と同権金員の
酸化物、塩化動勢の化会物を助剤として使用することも
、この発明の範囲に含まれる。
The anticorrosion adhesive of the present invention is produced by blending the gold powder with the resin described above, and further blending a hardening accelerating dispersion/settling agent, etc., as necessary. In addition, A
It is also within the scope of the present invention to use, as an auxiliary agent, an oxide or chloride-based compound of the gold maple powder, rather than the gold maple powder.

以上のように、この発明の防錆接着剤は、接合すべき金
員材料中の金員成分よりもイオン化傾向の大な#t@の
粉末が防錆剤として配合されているため、接着剤の接着
力をあまり低下させることなく充分な防錆効果を発揮し
うるのである。
As described above, the rust-preventive adhesive of the present invention contains #t@ powder, which has a greater ionization tendency than the metal component in the metal materials to be bonded, as a rust preventive agent. It is possible to exhibit a sufficient rust prevention effect without significantly reducing the adhesive strength of the adhesive.

つjに、実施列について比較列と併せて説明する。First, the implementation column will be explained together with the comparison column.

〔実施例1〜4.比較例1〕 接着剤および金員粉末等として次表に示すようプjもの
をIn2表に示す菫だけ配合し、防錆接着剤をつくった
。つぎに、得られた防錆接着剤を、トリクレンで脱脂さ
れた鉄板に5〜10μの厚みで塗布し、同じくトリクレ
ンで脱脂された鉄板と重ね合わせ、その状態で接着剤を
充分反応硬化させ、その接着強度(剥離強度)を測定し
た。また、固接層剤を脱脂鋼板のうえに5〜10μ塗布
し、充分に反応を通性させた。その試料に対1てJIS
K−5400に規定する塩水噴霧試験を実施した、その
結末は上記の第1表のとおりであり、実施−jのものの
防蛸力が漬れていることがわかる、◆日本アエロ/ル工
業製R−972(沈降防止剤)〔実JlilI例5〜1
01 金鵬粉末としてZn粉末を用いその配合量を下記の表の
ように変えた。それ以外は実施iQ1〜4と同様にして
防錆接着剤をつくり、その接着強度と塩水噴霧試験を実
施例1〜4と同様に実施した。
[Examples 1 to 4. Comparative Example 1] A rust-preventing adhesive was prepared by blending only the violet shown in the In2 table with the adhesive and metal powder shown in the following table. Next, the obtained rust-preventing adhesive is applied to a thickness of 5 to 10 μm on an iron plate that has been degreased with trichlene, and is overlapped with an iron plate that has also been degreased with trichlene, and the adhesive is fully reacted and cured in that state. The adhesive strength (peel strength) was measured. Further, 5 to 10 μm of the adhesive layer agent was applied onto the degreased steel plate to allow sufficient reaction permeability. JIS for that sample
A salt spray test specified in K-5400 was carried out, and the results are shown in Table 1 above, which shows that the anti-octopus ability of the one tested in test-j is poor. R-972 (anti-sedimentation agent) [Actual Jliil Examples 5-1
01 Zn powder was used as Kinho powder, and the blending amount was changed as shown in the table below. Other than that, anti-rust adhesives were prepared in the same manner as in Examples iQ1-4, and the adhesive strength and salt spray tests were conducted in the same manner as in Examples 1-4.

その結果は下記の第2表のとおりである。The results are shown in Table 2 below.

(以   下   余   白   )第2表より、金
@(Zn)粉末の配合量は、主剤の5−、−20倍に設
定することが好ましいことがわかる。
(See the margin below.) From Table 2, it can be seen that the amount of gold @ (Zn) powder to be blended is preferably set to 5-20 times the amount of the main ingredient.

〔実施例11〜16] 金鵬粉木として一片状Znおよび粒径が4μ、1〜1.
5μ、8μのZn粉末を用い、実施例1〜4とと同様に
して防錆接着剤をつくり、その接着強度と塩水噴霧試験
を実施例1〜4と同様に実施した。
[Examples 11 to 16] A piece of Zn was used as Kinpeng powder and the particle size was 4μ, 1 to 1.
Antirust adhesives were prepared in the same manner as in Examples 1 to 4 using Zn powders of 5μ and 8μ, and the adhesive strength and salt spray tests were conducted in the same manner as in Examples 1 to 4.

その結果は次の第3訝のとおりである。The result is the following third hypothesis.

(以   下   余   白   )◆l はしつき
が非冨に大きい→接着剤が不安定◆2 膜厚のにらっき
が太きすぎて信頼性乏しい小さすぎると接7m剤が安定
せず練入粒子が塗ahに残るため、強度もばらつくし、
防錆力も試料による差が多くなりすぎる。Znを粒状か
ら鱗片状にするとZnの皺が少電でも防鏑効果が充分期
待できるようになる。
(Left below) ◆l The adhesion is too large → the adhesive is unstable ◆2 The film thickness is too thick and unreliable. If it is too small, the adhesive will not be stable Since the injected particles remain in the coating, the strength also varies,
There are too many differences in rust prevention ability depending on the sample. When Zn is changed from granular to scaly, Zn wrinkles can be expected to have a sufficient anti-chilling effect even with a small amount of electric current.

〔実施例17〜19〕 主剤として変性アクリル樹脂を用い51i!、施−jl
〜4と同様にして防錆接着剤をつくり、その接着強度お
よび塩水噴霧試験を実jiII例1〜4と同様に実施し
た。その結果は下記の第4表のとおりであり、主剤を変
えても良好な結果が得られることがわがる0 (以   十   余   白   )第  4  表 秦l 接*性を高めるように改質した三菱レイヨン製#
l液1合特殊MMA樹脂(N、V25) 〔実施例20〜23〕 主剤としてアクリル樹脂、もしくはアクリル樹脂+反応
性塩化ビニル樹脂を用い実施例1〜4と同様にして防鯖
接盾創をつくり、その(硬質塩化ビニル樹脂)/(lj
クレン脱脂鉄板)に対する接着強度を6411 mする
とともに、防錆力を測定した。
[Examples 17 to 19] Using modified acrylic resin as the main ingredient, 51i! , Shi-jl
A rust-preventing adhesive was prepared in the same manner as in Examples 1 to 4, and its adhesive strength and salt spray tests were conducted in the same manner as in Examples 1 to 4. The results are shown in Table 4 below, and it can be seen that good results can be obtained even if the base agent is changed. Made by Mitsubishi Rayon #
1 liquid 1 mixture special MMA resin (N, V25) [Examples 20 to 23] Preparation of mackerel shield wounds in the same manner as in Examples 1 to 4 using acrylic resin or acrylic resin + reactive vinyl chloride resin as the main ingredient Construction, its (hard vinyl chloride resin)/(lj
The adhesive strength to a Clen degreased iron plate was determined to be 6411 m, and the rust prevention ability was also measured.

(−の結果は下B己の第5表のとおりである。(The results for - are shown in Table 5 below.

第5表 [− 接着強度: 防錆接着剤をトリクレン脱脂鉄板に5〜l
Oμ塗布して焼付けし、高温に 維持したまま、その上に硬質塩化ビニ ル樹脂シートを重ねて加圧接着した1、これを試料とし
、その接着強度を測定 した。
Table 5 [- Adhesive strength: 5 to 10 liters of anti-rust adhesive applied to a Triclean degreased iron plate.
After coating with Oμ and baking, a hard vinyl chloride resin sheet was layered and bonded under pressure while maintaining the temperature at high temperature. This was used as a sample and its adhesive strength was measured.

塩水噴訃謙:  JIS  K−5400に準拠して打
った。
Salt water fountain shot: Hit in accordance with JIS K-5400.

Claims (1)

【特許請求の範囲】 (11接合すべき金−材料中の金−成分よりもイオン化
傾向の大な金−の粉末が防錆剤として配合されているこ
とを特徴とする防錆接着剤、(2)金−粉末か、粒&2
〜6μのものである特許請求の範囲第1項記載の防錆接
着剤。 (3ン  金属粉末の配合菫が、X量基準でf&着剤(
主剤)の5〜20倍に設定されている特許請求の範囲第
1項または第2項記載の防錆接着剤。
[Scope of Claims] (11) A rust-preventing adhesive characterized in that a gold powder having a higher ionization tendency than the gold component in the gold-material to be bonded is blended as a rust preventive agent. 2) Gold - powder or grain &2
The anticorrosive adhesive according to claim 1, which has a particle diameter of 6 μm. (3) The blended violet of metal powder is based on the amount of f & adhesive (
The rust-preventing adhesive according to claim 1 or 2, wherein the rust-preventing adhesive is 5 to 20 times that of the main agent).
JP6308082A 1982-04-15 1982-04-15 Corrosion protecting adhesive Pending JPS58179279A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6308082A JPS58179279A (en) 1982-04-15 1982-04-15 Corrosion protecting adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6308082A JPS58179279A (en) 1982-04-15 1982-04-15 Corrosion protecting adhesive

Publications (1)

Publication Number Publication Date
JPS58179279A true JPS58179279A (en) 1983-10-20

Family

ID=13218996

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6308082A Pending JPS58179279A (en) 1982-04-15 1982-04-15 Corrosion protecting adhesive

Country Status (1)

Country Link
JP (1) JPS58179279A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05155065A (en) * 1991-12-05 1993-06-22 Fujitsu Ltd Printing head
KR20170038629A (en) * 2015-09-30 2017-04-07 엘에스전선 주식회사 Submarine cable having bimetallic armours
KR20170038628A (en) * 2015-09-30 2017-04-07 엘에스전선 주식회사 Submarine cable having bimetallic armours
US10475553B2 (en) 2015-09-30 2019-11-12 Ls Cable & System Ltd. Submarine cable having heterogeneous armor

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05155065A (en) * 1991-12-05 1993-06-22 Fujitsu Ltd Printing head
KR20170038629A (en) * 2015-09-30 2017-04-07 엘에스전선 주식회사 Submarine cable having bimetallic armours
KR20170038628A (en) * 2015-09-30 2017-04-07 엘에스전선 주식회사 Submarine cable having bimetallic armours
US10475553B2 (en) 2015-09-30 2019-11-12 Ls Cable & System Ltd. Submarine cable having heterogeneous armor

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