JPH0254432B2 - - Google Patents
Info
- Publication number
- JPH0254432B2 JPH0254432B2 JP14045084A JP14045084A JPH0254432B2 JP H0254432 B2 JPH0254432 B2 JP H0254432B2 JP 14045084 A JP14045084 A JP 14045084A JP 14045084 A JP14045084 A JP 14045084A JP H0254432 B2 JPH0254432 B2 JP H0254432B2
- Authority
- JP
- Japan
- Prior art keywords
- rust
- rust preventive
- iron
- copper
- alloys
- 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.)
- Expired
Links
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 48
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 20
- GTLQZNKUEFUUIS-UHFFFAOYSA-N carbonic acid;cyclohexanamine Chemical compound OC(O)=O.NC1CCCCC1 GTLQZNKUEFUUIS-UHFFFAOYSA-N 0.000 claims description 18
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 claims description 17
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 16
- 239000012964 benzotriazole Substances 0.000 claims description 16
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 12
- 239000011701 zinc Substances 0.000 claims description 12
- 229910052725 zinc Inorganic materials 0.000 claims description 12
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 11
- 239000010949 copper Substances 0.000 claims description 10
- 229910052802 copper Inorganic materials 0.000 claims description 10
- 229910000640 Fe alloy Inorganic materials 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 8
- 229910000881 Cu alloy Inorganic materials 0.000 claims description 7
- 239000003112 inhibitor Substances 0.000 claims description 6
- 238000005246 galvanizing Methods 0.000 claims description 2
- 230000003449 preventive effect Effects 0.000 description 28
- 239000003795 chemical substances by application Substances 0.000 description 16
- -1 galvanizing Chemical compound 0.000 description 13
- 230000002265 prevention Effects 0.000 description 10
- 229910052742 iron Inorganic materials 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- ZFAKTZXUUNBLEB-UHFFFAOYSA-N dicyclohexylazanium;nitrite Chemical compound [O-]N=O.C1CCCCC1[NH2+]C1CCCCC1 ZFAKTZXUUNBLEB-UHFFFAOYSA-N 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- PDDANVVLWYOEPS-UHFFFAOYSA-N nitrous acid;n-propan-2-ylpropan-2-amine Chemical compound [O-]N=O.CC(C)[NH2+]C(C)C PDDANVVLWYOEPS-UHFFFAOYSA-N 0.000 description 5
- 239000002904 solvent Substances 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000008016 vaporization Effects 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- 150000003852 triazoles Chemical class 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BFVIGZKFVVQUAG-UHFFFAOYSA-N 1h-benzimidazole-2,4-diamine Chemical compound C1=CC(N)=C2NC(N)=NC2=C1 BFVIGZKFVVQUAG-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910001297 Zn alloy Chemical group 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Landscapes
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
本発明は、鉄及び鉄合金、銅及び銅合金、亜
鉛、亜鉛メツキ、アルミニウムの気化性防錆剤に
関する。
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(DICHAN)
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ト(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的が殆んどないば
かりか、逆に腐食促進という悪影響を与える不都
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、他の金属に殆ど防錆効果がない不都
合がある。従つて、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。
本発明は、鉄及び鉄合金の他、銅及び銅合金、
亜鉛その他の非鉄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)とベンゾトリアゾール(BTA)又はト
リルトリアゾール(TTA)を重量比で99〜80対
1〜20の範囲の割合で混合して成る。
シクロヘキシルアンモニウムカーボネートとベ
ンゾトリアゾール又はトリルトリアゾールの混合
割合を重量比で99〜80対1〜20の範囲としたの
は、重量比でシクロヘキシルアンモニウムカーボ
ネート99に対してベンゾトリアゾール又はトリル
トリアゾールが1に満たない場合は鉄及び鉄合金
に対しての防錆効果はあるが、銅及び銅合金、亜
鉛、亜鉛メツキ、アルミニウムの非鉄金属品に変
色又は発錆が生じ、また重量比でシクロヘキシル
アンモニウムカーボネート80に対してベンゾトリ
アゾール又はトリルトリアゾールが20を超えた場
合は銅及び銅合金、亜鉛、亜鉛メツキに対しての
防錆効果はあるが、鉄及び鉄合金、アルミニウム
に変色又は発錆が生じる等の理由からである。
本願発明の防錆方法は、(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。
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、亜鉛メツキ、アルミニウムの夫々につき、
同じ形状、大きさの板状テストピースa5枚を、
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No.1〜21につきその各0.5gを不織布に
包んだもの3を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℃±0.5℃、湿
度100%に保持して25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。
その結果を表1に示す。表中、〇は異常なし、
△は発錆あり、×は発錆度大、××は発錆度非常に
大を示す。
防錆剤は、CHC、TTA、BTAの各単独とし
たサンプルNo.15、16、17、CHCとTTA又は
BTAを夫々配合割合(重量比)を変えて配合し
たサンプルNo.1〜14、CHCとメルカプトベンゾ
チアゾールを配合したサンプルNo.18、CHCとジ
アミノベンゾイミダゾールの配合サンプルNo.19、
亜硝酸ジイソプロピルアンモニウム(DIPAN)
の単独サンプルNo.20、DIPANとTTAの配合サン
プルNo.21を使用した。ブランクNo.22は防錆剤を使
用しない場合を示す。また、表1における防錆剤
の配合比は重量比である。
The present invention relates to a volatile rust preventive agent for iron and iron alloys, copper and copper alloys, zinc, galvanizing, and aluminum. Conventionally, dicyclohexylammonium nitrite (DICHAN) has been used as a volatile rust inhibitor for iron and iron alloys.
Nitrite amine salts such as nitrite amine salts and carboxylic acid amine salts such as cyclohexylammonium carbonate (CHC) are used, but they not only have almost no rust preventive effect on non-ferrous metals such as copper and zinc, but also have the opposite effect. This has the disadvantage of accelerating corrosion. Further, 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. 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 the separated steel parts and, for example, copper parts are treated separately. Rust prevention is carried out using the above-mentioned dedicated rust preventive agent, 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. In addition to iron and iron alloys, the present invention also includes copper and copper alloys,
This product provides a volatile rust preventive agent that has a rust preventive effect on zinc and other non-ferrous metals or their alloys, and contains cyclohexylammonium carbonate (CHC) and benzotriazole (BTA) or tolyltriazole (TTA) in a weight ratio. They are mixed at a ratio of 99 to 80 to 1 to 20. The reason why the mixing ratio of cyclohexylammonium carbonate and benzotriazole or tolyltriazole is in the range of 99 to 80 to 1 to 20 by weight is that the ratio of benzotriazole or tolyltriazole to 99 of cyclohexylammonium carbonate is less than 1. Although it has a rust prevention effect on iron and iron alloys, discoloration or rusting occurs on nonferrous metal products such as copper and copper alloys, zinc, galvanized, and aluminum. If benzotriazole or tolyltriazole exceeds 20, it has a rust preventive effect on copper and copper alloys, zinc, and galvanized plating, but it may cause discoloration or rust on iron, iron alloys, and aluminum. It is. The rust prevention method of the present invention includes (1) a method of directly spraying the above-mentioned mixed powder in the predetermined ratio onto the material to be rust-prevented, and (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. A method of storing powders in separate bags or in the same bag, vaporizing both, and bringing the mixture into contact with the rust-preventing material; A common method is to dissolve the seed powder in a solvent and apply or spray the solution onto the material to be rust-prevented. Fig. 1 shows an example of an apparatus for comparatively testing the effects of the rust preventive agent of the present invention.
For each of zinc, galvanized, and aluminum,
5 plate test pieces A of the same shape and size,
The container 1 is hung as shown in the figure, and in the center thereof, 0.5 g of each of rust preventives No. 1 to 21 shown in Table 1 are wrapped in non-woven fabric 3 is hung as shown in the figure.
After heating the water 4 placed in the bottom and keeping it at a temperature of 50°C ± 0.5°C and humidity of 100% for 25 days, each test piece was taken out and the presence or absence of rust and the state of rust were observed. . The results are shown in Table 1. In the table, 〇 indicates no abnormality.
△ indicates rusting, × indicates a large degree of rusting, and XX indicates a very large degree of rusting. The rust inhibitors were sample Nos. 15, 16, 17 with CHC, TTA, and BTA alone, and CHC and TTA or
Samples No. 1 to 14 containing BTA at different proportions (weight ratio), Sample No. 18 containing CHC and mercaptobenzothiazole, Sample No. 19 containing CHC and diaminobenzimidazole,
Diisopropylammonium nitrite (DIPAN)
Single sample No. 20 and combination sample No. 21 of DIPAN and TTA were used. Blank No. 22 shows the case where no rust preventive agent is used. Moreover, the compounding ratio of the rust preventive agent in Table 1 is a weight ratio.
【表】【table】
【表】【table】
【表】
上記表1から明らかなように、本発明の配合防
錆剤No.1〜No.10、即ちCHCとTTA又はBTAを
重量比で99〜80対1〜20の割合で配合したものの
みが、鉄、銅、亜鉛、亜鉛メツキ、アルミニウム
のいずれにも防錆効果を有することが認められ
た。又その他の鉄鋼、銅合金、亜鉛、亜鉛メツ
キ、アルミニウムについて同様の試験を行つたと
ころ表1と同様の結果を得た。
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つた。
即ち、STB鋼管eの両端開口部をポリエチレン
キヤツプ5,5で密閉し、そのキヤツプ5,5対
向面間の距離lを2mとし、その1端に試験すべ
き防錆剤3 0.5gを固定し、この状態で30日間
屋外放置した後、該鋼管eの内面の防錆効果を調
べた。防錆剤サンプルとしては、本発明防錆剤No.
3を亜硝酸ジシクロヘキシルアンモニウム
(DICHAN)と比較試験した。
その結果は、下記表2の通りであつた。[Table] As is clear from Table 1 above, the compounded rust preventives No. 1 to No. 10 of the present invention, that is, those containing CHC and TTA or BTA in a weight ratio of 99 to 80:1 to 20 It was found that only 100% had a rust-preventing effect on iron, copper, zinc, galvanized plating, and aluminum. Similar tests were conducted on other steels, copper alloys, zinc, galvanized, and aluminum, and results similar to those shown in Table 1 were obtained. Next, a vapor phase reach test was conducted on the rust preventive agent of the present invention using the testing apparatus shown in FIG. 2.
That is, the openings at both ends of the STB steel pipe e were sealed with polyethylene caps 5, 5, the distance l between the opposing surfaces of the caps 5 and 5 was set to 2 m, and 0.5 g of the rust preventive agent 3 to be tested was fixed to one end. After being left outdoors in this state for 30 days, the rust prevention effect on the inner surface of the steel pipe e was examined. As a rust preventive sample, this invention rust preventive agent No.
No. 3 was tested in comparison with dicyclohexylammonium nitrite (DICHAN). The results were as shown in Table 2 below.
【表】
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、本発明の防錆剤サンプルNo.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DICHANとDIPAN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。
又、本発明の防錆剤の溶剤に対する溶解度を比
較例DICHAN、DICHAN+DIPANと共に調べ
た結果下記表3に示す結果を得た。数字は各溶剤
(温度25℃)100g中の溶解量(%)で示す。[Table] As is clear from Table 2 above, it is recognized that the rust preventive agent of the present invention has a wide range of vaporization rust preventive performance. Also, regarding rust preventive sample No. 3 of the present invention,
The amount of volatilization was measured over time while the product was left open indoors at room temperature. The results are as shown in the vaporization characteristic curve A in Figure 3, which shows that it evaporates earlier than the comparatively tested rust inhibitor containing DICHAN and DIPAN (its characteristic curve B), and has superior initial rust prevention ability. It is also recognized that the volatile performance is excellent overall. Further, the solubility of the rust preventive of the present invention in a solvent was investigated together with comparative examples DICHAN and DICHAN+DIPAN, and the results shown in Table 3 below were obtained. The numbers are expressed as the amount dissolved (%) in 100g of each solvent (temperature 25°C).
【表】
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。
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
カーボネート(CHC)とトリアゾール類のうち
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、CHC対BTA
又はCHC対TTAとを重量比で99〜80対1〜20の
割合で配合した防錆剤として使用するので、その
CHC、BTA、TTAの各単独を防錆剤として使
用する場合と異なり、鉄又はその合金ばかりでは
なく銅又はその合金、亜鉛、亜鉛メツキ、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、銅、亜鉛などの異種金
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
向上した気化性防錆剤を提供する等の効果を有す
る。[Table] 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. As described above, according to the present invention, cyclohexylammonium carbonate (CHC) among carboxylic acid amine salts and particularly benzotriazole (BTA) or tolyltriazole (TTA) among triazoles are selected, and CHC versus BTA is selected.
Or, it is used as a rust preventive agent containing CHC and TTA in a weight ratio of 99 to 80 to 1 to 20.
Unlike when CHC, BTA, and TTA are used alone as rust preventive agents, the rust preventive effect is achieved not only on iron or its alloys, but also on nonferrous metals such as copper or its alloys, zinc, galvanized, and aluminum. To provide a volatile rust preventive agent that can prevent rust from assembling dissimilar metals such as iron, copper, and zinc without disassembling it, and has improved rust prevention range, initial rust prevention ability, and solubility in solvents. It has the effect of
第1図は防錆効果試験装置の1例の截断側面
図、第2図は気相到達試験装置の1部を截除した
截断側面図、第3図は粉末防錆剤の揮発特性曲線
を示すグラフである。
1…容器、2…蓋、3…防錆剤、4…水、5…
キヤツプ、a…テストピース、l…空間距離、A
…本発明防錆剤の揮発特性曲線。
Figure 1 is a cross-sectional side view of an example of the rust prevention effect testing device, Figure 2 is a cross-sectional side view with a part of the gas phase attainment test device removed, and Figure 3 is the volatile characteristic curve of the powder rust inhibitor. This is a graph showing. 1... Container, 2... Lid, 3... Rust preventive, 4... Water, 5...
Cap, a...test piece, l...spatial distance, A
...Volatilization characteristic curve of the rust inhibitor of the present invention.
Claims (1)
(CHC)とベンゾトリアゾール(BTA)又はト
リルトリアゾール(TTA)を重量比で99〜80対
1〜20の範囲の割合で混合して成る鉄及び鉄合
金、銅及び銅合金、亜鉛、亜鉛メツキ、アルミニ
ウムの気化性防錆剤。1 Iron and iron alloys, copper and copper alloys, zinc made by mixing cyclohexylammonium carbonate (CHC) and benzotriazole (BTA) or tolyltriazole (TTA) in a weight ratio of 99 to 80 to 1 to 20. , Volatile rust inhibitor for galvanizing and aluminum.
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 JPS6119786A (en) | 1986-01-28 |
| JPH0254432B2 true 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) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5631542B2 (en) * | 2008-11-10 | 2014-11-26 | 共栄社化学株式会社 | Rust preventive |
| JP6591026B1 (en) | 2018-11-01 | 2019-10-16 | 株式会社アイ・ティ・シ・コンサルティング | Reinforcing device for existing structure and attachment equipment for incidental facilities |
-
1984
- 1984-07-09 JP JP14045084A patent/JPS6119786A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6119786A (en) | 1986-01-28 |
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