JPH0718027B2 - Anti-corrosion paint - Google Patents
Anti-corrosion paintInfo
- Publication number
- JPH0718027B2 JPH0718027B2 JP26429692A JP26429692A JPH0718027B2 JP H0718027 B2 JPH0718027 B2 JP H0718027B2 JP 26429692 A JP26429692 A JP 26429692A JP 26429692 A JP26429692 A JP 26429692A JP H0718027 B2 JPH0718027 B2 JP H0718027B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- nitrite
- rust
- rust preventive
- paint
- 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 - Fee Related
Links
Landscapes
- Paints Or Removers (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
【0001】[0001]
【産業上の利用分野】この発明はコイル鉄心単板等の鉄
材の錆止めやジヤーマンシルバー(洋銀)の防錆用の錆
止め塗料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a rust preventive paint for rust prevention of iron materials such as coil iron core single plate and rust preventive of Jarman Silver (Western silver).
【0002】[0002]
【従来の技術】この種の防錆塗料としては本出願人が先
に提案した例えば特公昭61−47908号公報記載の
ものが有る。この従来の技術はエチルアルコール又はメ
チルアルコールの液体アルコール100〜1000部に
対して水0.5〜2部、亜硝酸ナトリウム又は亜硝酸カ
リウムの亜硝酸塩0.2〜0.6部、トリプロピルアミ
ン0.1〜3.0部をそれぞれ含有してなる防錆塗料
と、エチルアルコール又はメチルアルコールの液体アル
コール100〜1000部に対して水0.5〜3部、亜
硝酸ナトリウム又は亜硝酸カリウムの亜硝酸塩0.2〜
0.6部、トリプロピルアミン0.1〜2.0部、トリ
ブチルアミン0.1〜2.0部をそれぞれ含有してなる
防錆塗料である。2. Description of the Related Art As this kind of rust preventive paint, there is, for example, the one described in Japanese Patent Publication No. 61-47908 previously proposed by the present applicant. In this conventional technique, 0.5 to 2 parts of water, 0.2 to 0.6 parts of nitrite of sodium nitrite or potassium nitrite, and 0 to 3 parts of tripropylamine are used for 100 to 1000 parts of liquid alcohol such as ethyl alcohol or methyl alcohol. 0.5 to 3 parts of water, 100 to 1000 parts of liquid alcohol of ethyl alcohol or methyl alcohol, and nitrite salt of sodium nitrite or potassium nitrite. 0.2 ~
It is a rust preventive coating material containing 0.6 parts, 0.1 to 2.0 parts of tripropylamine and 0.1 to 2.0 parts of tributylamine, respectively.
【0003】[0003]
【発明が解決しようとする課題】前記した従来の技術は
製造後約1年間位は防錆効果良好であるが、製造後1年
3ケ月位経過すると、貯液ビン底部に三叉放射状の細か
い析出物が沈澱し堆積するようになり、防錆効果が著減
し、極細パイプ内の防錆塗工時にパイプ内が上記析出物
で詰まってしまうという問題点が有ることが判明した。The above-mentioned conventional technique has a good rust-preventing effect for about one year after the production, but after about one year and three months after the production, fine tri-radial precipitation is formed on the bottom of the storage bottle. It has been found that there is a problem that the substance is settled and accumulated, the anticorrosive effect is significantly reduced, and the pipe is clogged with the above-mentioned deposit during anticorrosion coating in the ultrafine pipe.
【0004】上記析出物の組成は定かではないが恐らく
は亜硝酸塩の粒子を核としてトリプロピルアミンやトリ
ブチルアミンなどの助けで亜硝酸塩が三叉放射状に成長
析出したものと思われる。Although the composition of the above-mentioned precipitate is not clear, it is considered that the nitrite grows and precipitates in a three-pronged radial pattern with the aid of tripropylamine, tributylamine, etc., using nitrite particles as nuclei.
【0005】いずれにしても前記従来の防錆塗料は製造
後約1年以上経過すると徐々に防錆効果が悪化するし、
安価なメチルアルコールを用いるとその蒸気による環境
汚染が生じ特に人体に対し害毒を与えるため、高価で無
毒のエチルアルコールの使用を余儀なくされていたとい
う問題点が有る。In any case, the above-mentioned conventional rust preventive coating composition gradually deteriorates in rust preventive effect after a lapse of about one year from the production,
The use of inexpensive methyl alcohol causes environmental pollution due to the vapor, which is particularly harmful to the human body. Therefore, there is a problem in that expensive and nontoxic ethyl alcohol must be used.
【0006】この発明は前記した各問題点を除去するた
めに、製造後長期に亘り防錆効果を持続できる防錆塗料
を安価に多量提供することを目的とする。In order to eliminate the above-mentioned problems, it is an object of the present invention to inexpensively provide a large amount of rust preventive paint capable of maintaining a rust preventive effect for a long period of time after production.
【0007】[0007]
【課題を解決するための手段】上記したこの発明の目的
は、水20〜100部に対し亜硝酸ナトリウムなどの亜
硝酸塩1.0〜4.0部を溶解してニトリロトリエタノ
ールアミン1〜5部加えて溶解するとともに、イソプロ
ピールアルコール1000部と混合し、さらにトリーn
ーブチルアミン1〜5部を加えて混合することで達成で
きる。The above-mentioned object of the present invention is to dissolve 1 to 5 parts of nitrilotriethanolamine by dissolving 1.0 to 4.0 parts of nitrite such as sodium nitrite in 20 to 100 parts of water. In addition to being dissolved, mixed with 1000 parts of isopropyl alcohol
It can be achieved by adding 1 to 5 parts of -butylamine and mixing.
【0008】[0008]
【作 用】各成分の限定理由を作用面から述べれば、イ
ソプロピールアルコールは稀釈剤として使用するが、そ
の速乾性と浸透拡散性とが本塗料の特性をなし、水は亜
硝酸塩を溶かすものであるが、イソプロピールアルコー
ル1000部に対し20部以下では亜硝酸塩の溶解が困
難になり、また100部以上では、時間の経過によりP
Hが低下してエマルジョン状に白濁する。[Working] Explaining the reason for limiting each component from the aspect of action, isopropyl alcohol is used as a diluent, but its quick-drying property and permeation-diffusion property form the characteristics of this paint, and water dissolves nitrite. However, with respect to 1000 parts of isopropyl alcohol, it is difficult to dissolve the nitrite when the amount is 20 parts or less, and when 100 parts or more, P
H decreases and becomes cloudy as an emulsion.
【0009】亜硝酸塩は防錆に使用するもので、1.0
部以下になると防錆効果が減少し、また4.0部以上で
は、乾燥すると塗布部が白色に結晶し、かつ高湿時に潮
解してよくない。Nitrite is used for rust prevention, and is 1.0
If the amount is less than 10 parts, the rust preventive effect is reduced, and if it is more than 4.0 parts, the applied part crystallizes white when dried and is not deliquescent at high humidity.
【0010】そしてトリーnーブチルアミンは防錆と共
にインヒビターつまり抑制剤として使用するが、1〜5
部の範囲内にあるを要する。And, tri-n-butylamine is used as an inhibitor or inhibitor together with rust prevention.
It is necessary to be within the range of the part.
【0011】ニトリロトリエタノールアミンは亜硝酸塩
が前記のように三叉放射状に生長析出する現象を防止す
ることができる。Nitrilotriethanolamine can prevent the phenomenon that nitrite grows out in a radial trifurcation as described above.
【0012】[0012]
【実施例】次にその実施例を説明する。 実施例 1 堯 NaNo2 (亜硝酸ナトリウム)2gをH2 O
(水)20ccに常温で混合し攪拌溶解させる。……試
料1 槇 上記試料1に常温雰囲気中でニトリロトリエタノー
ルアミン4gを加え混合する。……試料2 遙 試料2にイソプロピールアルコール1000ccを
混合し、さらにトリーnーブチルアミン4.5ccを常
温雰囲気中で加えて混合して本発明の防錆塗料を得た。EXAMPLES Next, examples will be described. Example 1 2 g of Toho NaNo 2 (sodium nitrite) was added to H 2 O.
(Water) 20 cc is mixed at room temperature and dissolved by stirring. …… Sample 1 Maki 4 g of nitrilotriethanolamine is added to and mixed with the above sample 1 in a normal temperature atmosphere. .. Sample 2 Haruka Sample 2 was mixed with 1000 cc of isopropyl alcohol, and 4.5 cc of tri-n-butylamine was added and mixed in a room temperature atmosphere to obtain an anticorrosive coating material of the present invention.
【0013】この例で冷延鋼板をピカピカになる迄磨い
て上記防錆塗料を塗布し乾燥した後フェリシアン化カリ
ウム(赤血塩)0.1gを水2ccに溶かした指示薬を
1滴(0.05cc)滴下したが無反応なので、刃物で
上記鋼板面を引掻いたが無反応であった。In this example, a cold-rolled steel plate was polished until it became shiny, and the above-mentioned anticorrosive paint was applied. After drying, 0.1 g of potassium ferricyanide (red blood salt) was dissolved in 2 cc of water to obtain 1 drop of indicator (0.05 cc). ) Although it was dropped, it was non-reactive, so the steel plate surface was scratched with a blade, but it was non-reactive.
【0014】無処理鋼板では同様なテストで50秒後明
瞭な斑点が発生しイオン反応があった(16℃、61
%) この実施例1による防錆塗料をスプレー法や浸漬法で鉄
心単板、純鉄薄板、丸棒表面、ジヤーマンシルバー薄板
表面、銅の薄片に防錆被膜を0.1〜0.5μm形成
し、上記材料を温度49℃±1℃相対湿度95%の恒温
恒湿槽内における高温高湿雰囲気中に4ケ月間放置後取
出してその尖鋭部を調査した結果、肉眼観察、顕微鏡観
察共防錆被膜の亀裂を初めとして錆の発生は全く認めら
れず、防錆塗料被膜は素材を刃物でかき削らなければ剥
離しなかった。In the same test, untreated steel sheet had an ionic reaction (50 ° C. at 61 ° C.) with clear spots after 50 seconds.
%) The anticorrosive coating according to this Example 1 was sprayed or dipped to obtain a core plate, pure iron sheet, round bar surface, Jarman silver sheet surface, copper sheet with an anticorrosive coating of 0.1 to 0.5 μm. After forming the above material, leaving it for 4 months in a high temperature and high humidity atmosphere in a constant temperature and humidity chamber at a temperature of 49 ° C ± 1 ° C and a relative humidity of 95%, and then taking it out and examining the sharpened portion, both macroscopic observation and microscopic observation were performed. No rust was found, including cracks in the rust preventive film, and the rust preventive paint film was not peeled off unless the material was scratched with a blade.
【0015】なおこの場合もフェリシアン化カリウム
(赤血塩)0.1gと水2ccとの混合溶液で発錆指示
テストを行なったが何んら指示反応は見受けられず完璧
なる防錆効果を確認できた。In this case as well, a rust indicating test was conducted with a mixed solution of 0.1 g of potassium ferricyanide (red blood salt) and 2 cc of water, but no indicating reaction was observed and a perfect rust preventive effect was confirmed. It was
【0016】そして、上記防錆塗料はその製造直後およ
び2年経過後共に、全体として無色透明でエマルジョ
ン、沈澱物、遊離物等は全く生じなく、化学的、物理的
な経時変化は全くなく安定であった。 実施例 2 堯 NaNo2 (亜硝酸ナトリウム)1gをH2 O
(水)70ccに常温で混合し攪拌溶解させる。……試
料1 槇 上記試料1に常温雰囲気中でニトリロトリエタノー
ルアミン1gを加え混合する。……試料2 遙 試料2にイソプロピールアルコール1000ccを
混合し、さらにトリーnーブチルアミン1.5ccを常
温雰囲気中で加え混合して本発明実施例2による防錆塗
料を得た。The above rust-preventive coating is colorless and transparent as a whole immediately after its production and after 2 years, and is free from emulsions, precipitates, loose substances, etc., and is stable with no chemical or physical change with time. Met. Example 2 1 g of Toho NaNo 2 (sodium nitrite) was added to H 2 O.
Mix 70 cc of (water) at room temperature and stir to dissolve. …… Sample 1 Maki 1 g of nitrilotriethanolamine is added to and mixed with the above sample 1 in a normal temperature atmosphere. .. Sample 2 Harm Sample 2 was mixed with 1000 cc of isopropyl alcohol, and 1.5 cc of tri-n-butylamine was added and mixed in a room temperature atmosphere to obtain an anticorrosive paint according to Example 2 of the present invention.
【0017】この例でも冷延鋼板をピカピカになる迄磨
いて上記防錆塗料を塗布し乾燥した後前記指示薬を1滴
(0.05cc)滴下したが無反応なので、刃物で上記
鋼板面を引掻いたが無反応であった。In this example as well, the cold rolled steel sheet was polished until it became shiny, and the rust preventive paint was applied and dried, and then one drop (0.05 cc) of the above indicator was dropped, but since it was non-reactive, the steel sheet surface was drawn with a blade. It was scratched but unresponsive.
【0018】無処理鋼板では同様なテストで50秒後明
瞭な斑点が発生しイオン反応があった(16℃、61
%) この実施例2による防錆塗料をスプレー法や浸漬法で鉄
心単板、純鉄薄板、丸棒表面に防錆被膜を0.1〜0.
5μm形成し、上記材料を温度49℃±1℃相対湿度9
5%の恒温恒湿槽内における高温高湿雰囲気中に4ケ月
間放置後取出して尖端部を調査した処、肉眼観察、顕微
鏡観察共防錆被膜の亀裂や錆の発生は全く認められず、
防錆塗料被膜は素材を炭素鋼刃物でかき削らなければ剥
離しなかった。In the same test, untreated steel sheet had an ionic reaction (50 ° C. at 61 ° C.) with clear spots after 50 seconds.
%) The rust-preventive coating according to this Example 2 was coated with a rust-preventive coating of 0.1 to 0.
5μm formed, the above material temperature 49 ℃ ± 1 ℃ relative humidity 9
After leaving it in a high temperature and high humidity atmosphere in a 5% constant temperature and humidity chamber for 4 months, it was taken out and the tip was inspected, and no cracks or rusts were observed in the rust preventive coating both with the naked eye and under the microscope.
The anticorrosive paint film did not peel unless the material was scratched with a carbon steel knife.
【0019】なおこの例でもフェリシアン化カリウムと
水との混合溶液の前記指示薬による発錆指示テストにお
いても全く発錆指示反応はなかった。Also in this example, there was no rusting indicating reaction in the rusting indicating test of the mixed solution of potassium ferricyanide and water with the above indicator.
【0020】そして、上記防錆塗料もその製造直後およ
び2年経過後共に、全体として無色透明でエマルジョ
ン、沈澱物、遊離物等は全く生じなく、化学的、物理的
な経時変化は全くなく安定であった。Immediately after the production of the rust-preventive paint and after 2 years, the rust-preventive paint was colorless and transparent as a whole, and no emulsions, precipitates, loose substances, etc. were formed, and there was no chemical or physical change with time and it was stable. Met.
【0021】なお亜硝酸ナトリウムの代りに亜硝酸カリ
ウムなどの他の亜硝酸塩を用いてもよい。Note that other nitrites such as potassium nitrite may be used instead of sodium nitrite.
【0022】[0022]
【発明の効果】この発明は以上説明したように構成した
ので、以下に記載の効果を奏する。ニトリロトリエタノ
ールアミン1〜5部を約1000部の防錆塗料中に混合
したので、前記従来技術における三叉放射状の結晶析出
物質の析出を長期に亘り確実に防止でき、かつ所期の防
錆効果も長期間保証できたという大きな効果が得られ
た。Since the present invention is constructed as described above, it has the following effects. Since 1 to 5 parts of nitrilotriethanolamine was mixed in about 1000 parts of the anticorrosion paint, it is possible to reliably prevent the formation of the tridentate radial crystal deposit material in the above-mentioned conventional technique for a long period of time, and also to obtain the desired anticorrosion effect. The great effect of being able to guarantee for a long time was obtained.
【0023】また特にこの発明では防錆効果の経年変化
もなく温度変化・紫外線などの化学的物理的変化に対し
安定かつ無色透明な防錆剤を極めて安価に多量提供する
ことが可能であるというような多くの利点があり、その
工業的効果は大である。In particular, according to the present invention, it is possible to provide a large amount of a colorless and transparent rust preventive which is stable and stable against changes in temperature and chemical / physical changes such as ultraviolet rays without aging change of rust preventive effect. There are many advantages, and its industrial effect is great.
Claims (1)
ムなどの亜硝酸塩1.0〜4.0部を溶解してニトリロ
トリエタノールアミン1〜5部加えて溶解するととも
に、イソプロピールアルコール1000部と混合し、さ
らにトリーnーブチルアミン1〜5部を加えて混合して
なる防錆塗料。1. 1.0 to 4.0 parts of nitrite such as sodium nitrite is dissolved in 20 to 100 parts of water, and 1 to 5 parts of nitrilotriethanolamine is added and dissolved therein, and 1000 parts of isopropyl alcohol is added. A rust preventive paint obtained by mixing and further adding 1 to 5 parts of tri-n-butylamine and mixing.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26429692A JPH0718027B2 (en) | 1992-09-07 | 1992-09-07 | Anti-corrosion paint |
MYPI93001100A MY109830A (en) | 1992-09-07 | 1993-06-08 | Rust preventive coating. |
CN 93108009 CN1033923C (en) | 1992-09-07 | 1993-07-07 | Rust preventive coating |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26429692A JPH0718027B2 (en) | 1992-09-07 | 1992-09-07 | Anti-corrosion paint |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0688259A JPH0688259A (en) | 1994-03-29 |
JPH0718027B2 true JPH0718027B2 (en) | 1995-03-01 |
Family
ID=17401205
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP26429692A Expired - Fee Related JPH0718027B2 (en) | 1992-09-07 | 1992-09-07 | Anti-corrosion paint |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPH0718027B2 (en) |
CN (1) | CN1033923C (en) |
MY (1) | MY109830A (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6353130A (en) * | 1986-08-23 | 1988-03-07 | Fuji Heavy Ind Ltd | Control device for continuously variable transmission |
JP5712341B2 (en) * | 2008-11-19 | 2015-05-07 | 中部キレスト株式会社 | Rust preventive composition |
CN102690544A (en) * | 2012-06-12 | 2012-09-26 | 天长市巨龙车船涂料有限公司 | Antirust coating, antirust method and application of antirust coating |
CN104073805A (en) * | 2014-07-08 | 2014-10-01 | 森鹤乐器股份有限公司 | Method for preparing anti-rusting liquid for piano tuning peg |
CN104342030A (en) * | 2014-11-14 | 2015-02-11 | 无锡伊佩克科技有限公司 | Antirust coating for steel plate and preparation method for antirust coating |
CN105969194A (en) * | 2016-07-19 | 2016-09-28 | 任新根 | Waterproof, anti-corrosion and anti-rust coating for metal |
CN107011765A (en) * | 2017-02-15 | 2017-08-04 | 滁州金桥德克新材料有限公司 | Railway steel bridge application water proof anti-corrosive paint and preparation method thereof |
CN107815161A (en) * | 2017-09-22 | 2018-03-20 | 镇江市太浪新材料科技有限公司 | A kind of antirusting agent for coating |
CN107903735A (en) * | 2017-11-28 | 2018-04-13 | 苏州卓诚钛设备有限公司 | A kind of preparation process of surface of metal product coating |
CN108080675A (en) * | 2017-12-27 | 2018-05-29 | 苏州塔比诺机电有限公司 | A kind of portable power tool |
CN108061380A (en) * | 2017-12-27 | 2018-05-22 | 苏州塔比诺机电有限公司 | A kind of Intelligent warm air blower with antirust body |
-
1992
- 1992-09-07 JP JP26429692A patent/JPH0718027B2/en not_active Expired - Fee Related
-
1993
- 1993-06-08 MY MYPI93001100A patent/MY109830A/en unknown
- 1993-07-07 CN CN 93108009 patent/CN1033923C/en not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
---|
実開昭56−78873(JP,U)) |
Also Published As
Publication number | Publication date |
---|---|
CN1083834A (en) | 1994-03-16 |
JPH0688259A (en) | 1994-03-29 |
MY109830A (en) | 1997-08-30 |
CN1033923C (en) | 1997-01-29 |
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