JPS6119786A - Vaporizable rust inhibitor of zinc - Google Patents

Vaporizable rust inhibitor of zinc

Info

Publication number
JPS6119786A
JPS6119786A JP14045084A JP14045084A JPS6119786A JP S6119786 A JPS6119786 A JP S6119786A JP 14045084 A JP14045084 A JP 14045084A JP 14045084 A JP14045084 A JP 14045084A JP S6119786 A JPS6119786 A JP S6119786A
Authority
JP
Japan
Prior art keywords
rust
iron
zinc
copper
rust inhibitor
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
JP14045084A
Other languages
Japanese (ja)
Other versions
JPH0254432B2 (en
Inventor
Shigemi Kurihara
栗原 成美
Shuichi Okamoto
秀一 岡本
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.)
KIYOUEISHIYA YUSHI KAGAKU KOGYO KK
Honda Motor Co Ltd
Kyoeisha Chemical Co Ltd
Original Assignee
KIYOUEISHIYA YUSHI KAGAKU KOGYO KK
Honda Motor Co Ltd
Kyoeisha Chemical 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 KIYOUEISHIYA YUSHI KAGAKU KOGYO KK, Honda Motor Co Ltd, Kyoeisha Chemical Co Ltd filed Critical KIYOUEISHIYA YUSHI KAGAKU KOGYO KK
Priority to JP14045084A priority Critical patent/JPS6119786A/en
Publication of JPS6119786A publication Critical patent/JPS6119786A/en
Publication of JPH0254432B2 publication Critical patent/JPH0254432B2/ja
Granted legal-status Critical Current

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  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Abstract

PURPOSE:To provide a vaporizable rust inhibitor developing rust inhibiting effect even to a non-ferrous metal such as copper or zinc or an alloy thereof other than iron and an iron alloy, obtained by mixing cyclohexylammonium carbonate and benzotriazole or tolyltriazole in a predetermined ratio. CONSTITUTION:A vaporizable rust inhibitor is prepared by mixing 99-80pts.wt. of cyclohexylammonium carbonate (CHC) and 1-20pts.wt. of benzotriazole (BTA) or tolyltriazole (TTA). This rust inhibitor is different from such a case that each of CHC, BTA and TTA is used alone as a rust inhibitor and develops rust inhibiting effect not only to iron or an iron alloy but also to a non-ferrous metal such as copper, a copper alloy, zinc, zinc plating or Al. Therefore, an assembled product comprising different metals such as iron and copper can be inhibited from rust without disassembling the same.

Description

【発明の詳細な説明】 従来、鉄及び鉄合金用気化性防錆剤として、亜硝酸ジシ
クロヘキシルアンモニウム(D工0HAN)などの亜硝
酸アミン塩類又はシクロヘキシルアンモニウムカーボネ
ー)(CHC)などのカルボン酸アミン塩類が夫々使用
されているが、銅、亜鉛などの非鉄金属に対し防錆効果
が殆んどないばかりか、逆に腐食促進という悪影譬を与
える不都合がある。又、銅及び銅合金用気化性防錆剤と
して、ベンゾトリアゾール(BTA)、トリルトリアゾ
ール(TTA)などのトリアゾール類が使用されている
が、他の金属に殆んど防錆効果がない不都合がある。従
って、従来、鉄鋼部品と他の非鉄金属部品の組合せ品に
対して防錆する場合、鉄鋼部品と他の非鉄金属部品とを
分離して、その分離した鉄鋼部品と例えば銅部品とにつ
き夫々専用の前記防錆剤を使用し防錆することが行なわ
れ、その防錆処理が1面倒であり、亜鉛又は亜鉛合金部
品がある場合は、これに対し防錆効果がないばかりか鉄
又は鉄合金部品との組合せ品で分離不可能の場合は、そ
の腐蝕を回避することができない不都合がある。
Detailed Description of the Invention Conventionally, nitrite amine salts such as dicyclohexylammonium nitrite (DOHHAN) or carboxylic acid amines such as cyclohexylammonium carbonate (CHC) have been used as volatile rust inhibitors for iron and iron alloys. Although salts are used, they not only have almost no rust-preventing effect on non-ferrous metals such as copper and zinc, but they also have the disadvantage of accelerating corrosion. In addition, triazoles such as benzotriazole (BTA) and tolyltriazole (TTA) are used as volatile rust preventive agents for copper and copper alloys, but they have the disadvantage that they have almost no rust preventive effect on other metals. be. Therefore, conventionally, when rust-preventing a combination of steel parts and other non-ferrous metal parts, the steel parts and other non-ferrous metal parts are separated, and each of the separated steel parts and, for example, a copper part, has its own dedicated Rust prevention is carried out using the above-mentioned rust inhibitors, but the rust prevention treatment is troublesome, and if there are zinc or zinc alloy parts, it not only has no rust prevention effect, but also iron or iron alloy parts. If the product is a combination of parts that cannot be separated, there is an inconvenience that corrosion cannot be avoided.

本発明は、鉄及び鉄合金の他銅及び銅合金、亜鉛その他
の非金属又はその合金に対しても防錆効果をもたらす気
化性防錆剤を提供するもので、シクロヘキシルアンモニ
ウムカーボネート(CHC)99〜80対ベンゾトリア
ゾール(B T A)又はトリルトリアゾール(TTA
)1〜20の範囲の割合で混合して成る。
The present invention provides a volatile rust preventive agent that has a rust preventive effect on iron and iron alloys as well as copper and copper alloys, zinc and other nonmetals, and their alloys. ~80 pairs benzotriazole (BTA) or tolyltriazole (TTA
) are mixed at a ratio in the range of 1 to 20.

本発明の防錆方法は、(1)上記所定割合の混合粉末と
して直接被防錆材に散布する方法、(2)被防錆材を密
封した容器内に、上記の配合すべき2種の粉末の夫々を
各別の袋などに入れたもの又は同じ袋などに混入したも
のを収容し、両者を気化させその混合気を被防錆材に接
触させる方法、(3)その所定割合の2種の粉末を溶“
剤に溶かして、その溶液を被防錆材に塗布又は噴霧する
方法などが一般である。
The rust prevention method of the present invention includes (1) a method of directly spraying the above-mentioned mixed powder as a predetermined ratio onto the material to be rust-prevented; (2) a method in which the above-mentioned two types of material to be mixed are mixed in a sealed container with the material to be rust-prevented; (3) A method of storing powders in separate bags or the same bag, vaporizing both, and bringing the mixture into contact with the rust-preventing material; Dissolve the seed powder
A common method is to dissolve it in an agent and apply or spray the solution onto the rust preventive material.

第1図は、本発明の防錆剤の効果を比較試験するための
装置の1例を示し、角型ポリエチレン容器(1)に蓋(
2)を密栓し、その蓋(2)の下面に鉄、銅、亜鉛、亜
鉛メッキ材の夫々につき、同じ形状、大きさの板状テス
トピース&5枚を7、図示のように吊り下げ、その中央
に表1に夫々示す防錆剤A1〜21につきその各o、 
s g f:不織布に包んだもの(3)全図示のように
吊り下げ、該容器(1)底部に入れた水(4)を加熱し
温度50℃±α5゛C1湿度100%に保持して20日
間放置した後、各テストピースを取り出し、その夫々に
つき錆の発生の有無、錆の状態を観、察した。
FIG. 1 shows an example of an apparatus for comparatively testing the effects of the rust preventive agent of the present invention.
2), and hang 5 plate test pieces of the same shape and size for each of iron, copper, zinc, and galvanized materials on the underside of the lid (2) as shown in the figure. In the center, each of the rust inhibitors A1 to 21 shown in Table 1,
s g f: Wrapped in non-woven fabric (3) Suspended as shown in the figure, heated the water (4) placed in the bottom of the container (1) and maintained at a temperature of 50°C ± α5゛C1 humidity 100%. After being left for 20 days, each test piece was taken out and the presence or absence of rust and the state of the rust were observed and observed.

その結果を表IVC示す。表中、○は異常なし、△は発
錆あり、×は発錆度大、××は発錆度非常に大を示す。
The results are shown in Table IVC. In the table, ○ indicates no abnormality, △ indicates rust, × indicates a high degree of rust, and XX indicates a very high degree of rust.

防錆剤は、0)10.TTASBTAの各単独、サンプ
ル應15.16.170HoとTTA又はBTAを夫々
配合割合(重量比)′t−変えて配合したサンプル&1
〜14、OHOとメルカプトベンゾチアゾールを配合し
たサンプル轟18、OHOとジアミノベンゾイミダゾー
ルの配合サンプルA19、亜硝酸ジイソプロピルアンモ
ニ1)A (DIPAN)単独’Fjンブ#A20゜D
IPANと’fTAの配合サンプル&21f使用シた。
The rust preventive agent is 0)10. TTASBTA alone, sample 15, 16, 170Ho and TTA or BTA at different blending ratios (weight ratio)'t - Sample &1
~14, Sample Todoroki with a combination of OHO and mercaptobenzothiazole 18, Sample A19 with a combination of OHO and diaminobenzimidazole, Diisopropylammoninitrite 1) A (DIPAN) alone 'Fj combination #A20゜D
IPAN and 'fTA combination sample & 21f usage sample.

ブランクA22は防錆剤を使用しない場合を示す。Blank A22 shows the case where no rust preventive agent is used.

上記表から明らかなように、本発明の配合防錆剤A1〜
A10、即ち、重量比で01099〜80とTTA又は
BTA 1〜20の割合で配合したもののみが1鉄、鋼
、亜鉛メッキ、アルミニウムのいづれにも防錆効果を有
することが認められた。その他の鉄鋼、銅合金、亜鉛、
亜鉛メッキ、アルミニウムについて同様の試験を行ない
表1と同様の結果を得た。
As is clear from the above table, the compounded rust preventive agent A1 of the present invention
It was found that only A10, that is, a mixture of 01099 to 80 and TTA or BTA in a weight ratio of 1 to 20, had a rust-preventing effect on any of iron, steel, galvanized, and aluminum. Other steels, copper alloys, zinc,
Similar tests were conducted on zinc plating and aluminum, and results similar to those shown in Table 1 were obtained.

次に、上記本発明の防錆剤につき気相到達距離試験を第
2図に示す試験装置を使用し行なった。即ち、STB鋼
管eの両端開口部をポリエチレンキャラ7’ t5J 
[5)で密閉し、そのキャップ(51f51対向面間の
距離1 ft2 mとし、その1端に試験すべき防錆剤
(3)α5gを固定し、この状態で、30日問屋外放置
した後、該鋼管eの内面の防錆効果を測べた。防錆剤サ
ンプルとしては、本発明防錆剤&3を亜硝酸ジシクロヘ
キシルアンモニウム(D工aHhH)と比較試験した。
Next, a vapor phase reach test was conducted on the rust preventive agent of the present invention using the test apparatus shown in FIG. 2. That is, the openings at both ends of the STB steel pipe e are covered with polyethylene characters 7't5J.
[5), the cap (distance between the opposing surfaces of 51f51 is 1 ft2 m), and the rust preventive agent (3) α5g to be tested is fixed to one end of the cap, and in this state, it is left outdoors for 30 days. The rust preventive effect on the inner surface of the steel pipe e was measured. As a sample of the rust preventive agent, the rust preventive agent &3 of the present invention was tested in comparison with dicyclohexyl ammonium nitrite (D-AHhH).

その結果は、下記表2の通りであった。The results were as shown in Table 2 below.

表  2 上記表2から明らかなように、本発明防錆剤は広範囲な
気化防錆性能を有していることが認められる。又、本発
明の防錆剤例えばサンプル黒3につき、常温で屋内開放
放置状態で揮発量を経時的に測定した。その結果は第3
図の気化特性曲線Aに示す通りで、比較試験したDIj
OHAMとD工PANを配合した防錆剤(その特性曲線
B)に比し早期に揮発し、初期防錆力に優れていると共
に全体としても揮発性能が優れていることが認められる
。
Table 2 As is clear from Table 2 above, it is recognized that the rust preventive of the present invention has a wide range of vaporization rust preventive properties. Further, the amount of volatilization of the rust preventive agent of the present invention, such as Sample Black 3, was measured over time while it was left open indoors at room temperature. The result is the third
As shown in the vaporization characteristic curve A in the figure, the comparatively tested DIj
Compared to the rust inhibitor containing OHAM and D-PAN (its characteristic curve B), it volatilizes earlier, exhibits excellent initial rust prevention ability, and is recognized to have excellent overall volatilization performance.

又、本発明の防錆剤の溶剤に対する溶解度を、検べた結
果下記表3に示す結果を得た。数字は、各溶剤(25℃
)100g中の溶解量(%)で示す。
Further, the solubility of the rust preventive agent of the present invention in a solvent was examined, and the results shown in Table 3 below were obtained. The numbers are for each solvent (25℃
) Dissolved amount (%) in 100g.

表  3 表3から明らかなように、本発明防錆剤は、比較的濃厚
な液状防錆剤を提供することができ有利である。
Table 3 As is clear from Table 3, the rust preventive agent of the present invention is advantageous in that it can provide a relatively concentrated liquid rust preventive agent.

このように本発明によるときは、カルボン酸アミン塩類
のうち特にシクロヘキシルアンモニウムカーボネー)(
01(0)とトリアゾール環類のうち特にベンゾトリア
ゾール(BTA)又はトリルトリアゾール(TTA)と
を選択し、010対BTA又はOHO対TTAとを99
〜80対1〜20の割合で配合した防腐剤として使用す
るので、そのOHO,BTASTTAの各単独を防腐剤
として使用する場合と異なり、鉄又はその合金ばかりで
なく銅又はその合金、亜鉛、亜鉛メッキ、アルミニウム
などの非鉄金属についても防錆効果を発揮する効果をも
たらし、鉄と銅などの異種金属の組立て品を分解するこ
となく防錆でき、又その防錆範囲、初期防錆力、溶剤に
対する溶解度の向上した防錆剤を提供する等の効果を有
する。
Thus, according to the present invention, among the carboxylic acid amine salts, especially cyclohexylammonium carbonate) (
01 (0) and triazole rings, benzotriazole (BTA) or tolyltriazole (TTA) is selected, and 010 vs. BTA or OHO vs. TTA is 99
Since it is used as a preservative in a ratio of ~80 to 1 to 20, unlike the case where OHO and BTASTTA are used alone as a preservative, not only iron or its alloys but also copper or its alloys, zinc, and zinc are used as preservatives. It has a rust-preventing effect on non-ferrous metals such as plating and aluminum, and can prevent rust from assembling dissimilar metals such as iron and copper without disassembling it. This has the effect of providing a rust preventive agent with improved solubility in

【図面の簡単な説明】[Brief explanation of the drawing]

2fTJ1図は防錆効果試験装置の1例の裁断側面図、
第2図は気相到達試験装置の1部を截除した裁断側面図
、第5図は粉末防錆剤の揮発特性面at示すグラフであ
る。 (1)・・・容  器 (2)・・・蓋 (3)・・・防錆剤 (4)・・・水 (5)・・・キャップ a・・・テストピース ト・・空間距離
Figure 2fTJ1 is a cut side view of an example of the rust prevention effect testing device.
FIG. 2 is a cut-away side view of a part of the vapor phase attainment test apparatus, and FIG. 5 is a graph showing the volatile characteristic surface at of the powder rust preventive agent. (1) Container (2) Lid (3) Rust preventive agent (4) Water (5) Cap a Test piece Space distance

Claims (1)

【特許請求の範囲】 シクロヘキシルアンモニウムカーボネート (CHC)99〜80対ベンゾトリアゾール(BTA)
又はトリルトリアゾール(TTA)1〜20の範囲の割
合で混合して成る亜鉛等の気化性防錆剤。
[Claims] Cyclohexylammonium carbonate (CHC) 99-80 vs. benzotriazole (BTA)
Or a volatile rust preventive agent such as zinc mixed with tolyltriazole (TTA) in a ratio ranging from 1 to 20 parts.
JP14045084A 1984-07-09 1984-07-09 Vaporizable rust inhibitor of zinc Granted JPS6119786A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14045084A JPS6119786A (en) 1984-07-09 1984-07-09 Vaporizable rust inhibitor of zinc

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14045084A JPS6119786A (en) 1984-07-09 1984-07-09 Vaporizable rust inhibitor of zinc

Publications (2)

Publication Number Publication Date
JPS6119786A true JPS6119786A (en) 1986-01-28
JPH0254432B2 JPH0254432B2 (en) 1990-11-21

Family

ID=15268900

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14045084A Granted JPS6119786A (en) 1984-07-09 1984-07-09 Vaporizable rust inhibitor of zinc

Country Status (1)

Country Link
JP (1) JPS6119786A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010111934A (en) * 2008-11-10 2010-05-20 Kyoeisha Chem Co Ltd Rust-preventive agent
US11286680B2 (en) 2018-11-01 2022-03-29 Itc Consulting Inc. Reinforcement device for existing structure and incidental facility attaching device

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010111934A (en) * 2008-11-10 2010-05-20 Kyoeisha Chem Co Ltd Rust-preventive agent
US11286680B2 (en) 2018-11-01 2022-03-29 Itc Consulting Inc. Reinforcement device for existing structure and incidental facility attaching device

Also Published As

Publication number Publication date
JPH0254432B2 (en) 1990-11-21

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