JPH02243785A - Protection - Google Patents

Protection

Info

Publication number
JPH02243785A
JPH02243785A JP2024997A JP2499790A JPH02243785A JP H02243785 A JPH02243785 A JP H02243785A JP 2024997 A JP2024997 A JP 2024997A JP 2499790 A JP2499790 A JP 2499790A JP H02243785 A JPH02243785 A JP H02243785A
Authority
JP
Japan
Prior art keywords
group
formula
metal surface
organic medium
metal
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
JP2024997A
Other languages
Japanese (ja)
Inventor
Robert Montgomery O'neil
ロバート モントゴメリ オー’ネイル
Peter C Hamblin
ピーター シー.ハムブリン
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.)
Novartis AG
Original Assignee
Ciba Geigy AG
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 Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of JPH02243785A publication Critical patent/JPH02243785A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • C23F11/14Nitrogen-containing compounds
    • C23F11/141Amines; Quaternary ammonium compounds
    • C23F11/142Hydroxy amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/04Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M133/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M133/08Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Lubricants (AREA)

Abstract

PURPOSE: To temporarily protect the surface of a metal in contact with the corrosive atmosphere from corrosion by dipping the metal surface in a nonpoisonous org. medium contg. a compd. shown by a specified formula and then removing the metal surface from the medium.
CONSTITUTION: The surface of a metal to be protected is dipped in a nonpoisonous org. medium contg. at least one kind of compd. shown by formula I, and then the metal surface is brought out from the medium. In formula I, R is a 12-20C straight-chain or branched alkyl or a group shown by formula II. In formula II, Ra is a 8-15C straight-chain or branched alkyl and arranged at position 3 or 4 of phenyl. The org. solvent to be used is the one with mineral oil, aromatic or aliphatic hydrocarbons, etc., as the base. The compd. of formula I is incorporated by 2-15wt.% into the solvent, and a rust inhibitor, dispersant and surfactant can be incorporated into the solvent. Consequently, the metal surface is temporarily protected easily and effectively.
COPYRIGHT: (C)1990,JPO

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は金属表面の一時的保護に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to temporary protection of metal surfaces.

〔従来の技術と発明が解決しようとする課題〕種々の基
質において、鉄金属のための持久的な酸化もしくは腐食
防止剤としての、エーテル系オレフィンオキシド類もし
くはグリシジルエーテル類とジェタノールアミン類の付
加物の使用は公知である。
[Prior Art and Problems to be Solved by the Invention] Addition of jetanolamines with etheric olefin oxides or glycidyl ethers as a durable oxidation or corrosion inhibitor for ferrous metals in various substrates. The use of objects is known.

例えば、米国特許明細書2856363号には、潤滑油
の酸化防止剤としての式: %式% (式中、R1は炭素原子数2ないし12のアルキル基、
R2は水素原子または炭素原子数2ないし12のアルキ
ル基、R8は炭素原子数2ないし5の炭化水素鎖そして
Y、は水素原子またはR,−OHを表す)を持つ化合物
の使用が記載されている。
For example, U.S. Pat. No. 2,856,363 describes the formula as an antioxidant for lubricating oils:
The use of compounds in which R2 is a hydrogen atom or an alkyl group having 2 to 12 carbon atoms, R8 is a hydrocarbon chain having 2 to 5 carbon atoms, and Y is a hydrogen atom or R, -OH is described. There is.

英国特許明細書1455476号には、鉱油し3ケの水
酸基により置換された炭素原子数2ないし5のアルキル
基を表す;但し、R7とRIlの少なくとも一つは水酸
基により置換されており、そしてXが一〇−を表すとき
はR6は分枝した炭素原子数4ないし20のアルキル基
を表す条件に従う)を持つ化合物の少なくとも一種を含
有する非水性の機能液が開示されている。
British Patent Specification No. 1455476 describes mineral oil as an alkyl group having 2 to 5 carbon atoms substituted with 3 hydroxyl groups; provided that at least one of R7 and RIl is substituted with a hydroxyl group, and Disclosed is a non-aqueous functional liquid containing at least one compound having the following condition: when 10-, R6 represents a branched alkyl group having 4 to 20 carbon atoms.

欧州特許252007号は、腐食防止剤として式: (式中、R1、RloおよびRIlは独立して、なかん
ずく水素原子または炭素原子数1ないし15のアルキル
基を表し;そしてR1□とRI3は独立して、水素原子
、2−ヒドロキシエチル基または2−ヒドロキシプロピ
ル基を表す;但し、a ) ’R、□とR13は同時に
水素原子を表さない; b)R+□とR11の各々が−CH,CH,OH基材、
過剰塩基性(overbased)のアルカリ土類金属
化合物の0.01−0.5重量パーセントおよび式: %式%)] (式中、R4は炭素原子数1ないし24の炭化水素基を
表しiRs、Y2およびZ、は水素原子または炭素原子
数1ないし10の炭化水素基を表しそしてxlはOまた
は1を表す)を持つ置換トリアルカノールアミンの少量
の錆防止量を含む錆防止潤滑油組成物が記述されている
European Patent No. 252007 discloses corrosion inhibitors of the formula: represents a hydrogen atom, a 2-hydroxyethyl group or a 2-hydroxypropyl group; however, a) 'R, □ and R13 do not represent a hydrogen atom at the same time; b) R+□ and R11 each represent -CH, CH,OH base material,
0.01-0.5 weight percent of an overbased alkaline earth metal compound and the formula: %formula%] (wherein R4 represents a hydrocarbon group having 1 to 24 carbon atoms; iRs; A rust-inhibiting lubricating oil composition comprising a small amount of a substituted trialkanolamine in which Y2 and Z represent a hydrogen atom or a C1-C10 hydrocarbon group and xl represents O or 1 It has been described.

英国特許公開公報2172284Aには、腐食防止剤と
して、式: %式% 〔式中、Xはなかんずく一〇−を表し;R6はなかんず
く炭素原子数2ないし6のアルキル基を表し;R7は単
置換の炭素原子数1ないし4のアルキル基または1ない
し3ケの水酸基により置換された炭素原子数2ないし5
のアルキル基を表し;そしてR8は水素原子、未置換の
炭素原子数1ないし4のアルキル基または1ないである
時、R7とR1゜は同時に水素原子を表さずそしてR1
゜はペンチル基を表さない;そしてC)ポリアルキレン
フェノールまたはポリカルボン酸エステルの共−添加剤
は存在しない。
British Patent Publication No. 2172284A describes corrosion inhibitors of the formula: %Formula % [wherein X is inter alia 10-; R6 is inter alia an alkyl group having 2 to 6 carbon atoms; R7 is a monosubstituted 2 to 5 carbon atoms substituted with 1 to 4 alkyl groups or 1 to 3 hydroxyl groups;
represents an alkyl group; and R8 is a hydrogen atom, an unsubstituted C1-C4 alkyl group, or 1 or less, R7 and R1° do not simultaneously represent a hydrogen atom, and R1
゜ does not represent a pentyl group; and C) there are no co-additives of polyalkylene phenols or polycarboxylic esters.

という条件に従う。subject to the conditions.

これら開示の各々は、金属表面と機能液体が接触状態に
ある間、該液体と接触している該表面の持久的腐食保護
を提供するための問題に関するものである。
Each of these disclosures is concerned with the problem of providing durable corrosion protection of metal surfaces in contact with a functional liquid while the surfaces are in contact with the liquid.

金属の腐食防止の分野において生じる他の問題は、更に
持久的処理を施す前または最終的施工環境:例えば腐食
防止剤を含有している機能液体と接触する環境に置く前
に、生産したでの金属表面を一時的に保護することの需
要があることである。
Another problem that arises in the field of corrosion protection of metals is that the production of as-produced metals before being subjected to further permanent treatment or in contact with the final construction environment, e.g. functional fluids containing corrosion inhibitors. There is a need for temporary protection of metal surfaces.

米国特許4315957号には、金属を一時的に被覆す
るようなものとして蝋組成物を使用し、そして金属の別
の腐食防止処理に先立って水蒸気により蝋塗膜を除くこ
とが提案されている。
U.S. Pat. No. 4,315,957 proposes using a wax composition as a temporary coating on metal and removing the wax coating with steam prior to further corrosion protection treatment of the metal.

米国特許4752336号には、金属表面に非常に薄い
容易に除くことのできる一時的保護の塗膜を施工する方
法が記載されており、この工程は揮発性のフッ化炭化水
素系溶媒中の特性を持たせた脂肪酸エステルの使用を包
含し、この溶媒は金属表面上に該エステルのフィルムを
残して留去することができる。該エステルは、予め決め
られた時間内に該表面から自己蒸発(自己除去: 5e
lf−re+noved)するのに充分な程度に揮発性
である。
U.S. Pat. No. 4,752,336 describes a method for applying a very thin, easily removable, temporary protective coating to metal surfaces, a process that is characterized by its properties in volatile fluorocarbon solvents. The solvent can be distilled off leaving a film of the ester on the metal surface. The ester self-evaporates (self-removes: 5e) from the surface within a predetermined time.
lf-re+noved).

[課題を解決するための手段] 我々は、金属表面に一時的保護を施す簡単かつ効果的な
方法を見出した。
SUMMARY OF THE INVENTION We have discovered a simple and effective method of providing temporary protection to metal surfaces.

該方法は、潜在的に危険なフルオロカーボン系溶媒の揮
発を避けながら、処理する金属表面を腐食防止剤の環境
的に受容できる有機溶液に簡単に浸漬することを包含す
る。
The method involves simply immersing the metal surface to be treated in an environmentally acceptable organic solution of a corrosion inhibitor while avoiding volatilization of potentially hazardous fluorocarbon-based solvents.

従って本発明は: 少なくとも式I R−0−Clh−Ctl(Off)CH2N(CHzC
H20H)z  (1)ル基およびtert−オクタデ
シル基、またはこれらの混合物を表す。Rの好ましい基
は炭素原子数12ないし14のアルキル基を表す。
The invention therefore provides: at least the formula I R-0-Clh-Ctl(Off)CH2N(CHzC
H20H)z (1) Represents a ru group and a tert-octadecyl group, or a mixture thereof. A preferred group for R is an alkyl group having 12 to 14 carbon atoms.

炭素原子数8ないし15のアルキル基R″は例えばn−
オクチル基、n−ノニル基、n−デシル基、n−ドデシ
ル基、n−)リゾシル基、n−テトラデシル基、n−ペ
ンタデシル基、1sO−オクチル基、tert−オクチ
ル基、1so−ノニル基、tert−ノニル基、1so
−デシル基、tert−ドデシル基およびjert−ペ
ンタデシル基またはこれらの混合物である。R″の好ま
しい基は炭素原子数9ないし15のア、ルキル基を表す
C8 -C15 alkyl R'' is, for example, n-
Octyl group, n-nonyl group, n-decyl group, n-dodecyl group, n-)lysosyl group, n-tetradecyl group, n-pentadecyl group, 1sO-octyl group, tert-octyl group, 1so-nonyl group, tert -nonyl group, 1so
-decyl group, tert-dodecyl group and jert-pentadecyl group or a mixture thereof. A preferred group for R'' is an alkyl group having 9 to 15 carbon atoms.

式■の好ましい化合物は、式中Rが4−ノニルフェニル
基、4−ドデシルフェニル基、3ペンタデシルフエニル
基、ドデシル基またはテトラデシル基またはこれらの混
合物である。
Preferred compounds of formula (1) are those in which R is a 4-nonylphenyl group, 4-dodecylphenyl group, 3-pentadecylphenyl group, dodecyl group or tetradecyl group, or a mixture thereof.

式■の化合物の溶液を形成するのに使用してもよい有機
溶媒は例えば、鉱油、芳香族もしくは脂肪族炭化水素ま
たは他のペトロリウムスピ〔式中、Rは炭素原子数12
ないし20の直鎖のもしくは分枝したアルキル基、また
は式■:(式中、R”は炭素原子数8ないし15の直鎖
のもしくは分枝したアルキル基を表し、そしててフェニ
ル基の3または4位に配置されている)を持つ基を表す
〕を持つ化合物の少なくとも一種を含有する環境的に受
容できる有機媒体中に、保護されるべき金属表面を浸漬
し、次いで該金属表面を該媒体から取り去ることを包含
する、腐食性大気に接触している該金属表面、特に鉄金
属表面に一時的な腐食防止保護を施す方法である。
Organic solvents which may be used to form a solution of the compound of formula (1) are, for example, mineral oil, aromatic or aliphatic hydrocarbons or other petroleum solvents (wherein R has 12 carbon atoms).
a straight-chain or branched alkyl group having 8 to 20 carbon atoms, or a straight-chain or branched alkyl group having 8 to 15 carbon atoms, or a phenyl group of 3 or The metal surface to be protected is immersed in an environmentally acceptable organic medium containing at least one compound with a A method of providing temporary anti-corrosion protection to metal surfaces, especially ferrous metal surfaces, in contact with corrosive atmospheres, including removal from corrosive atmospheres.

炭素原子数12ないし20のアルキル基Rの例は、例え
ばn−ドデシル基、n−1−リゾシル基、n−テトラデ
シル基、n−ヘキサデシル基、n−オクタデシル基、n
−アイコシル基、tert−ドデシル基、tert−ヘ
キサデシリフト(petroleum 5pirit)
を基材とする溶媒である。
Examples of the alkyl group R having 12 to 20 carbon atoms include n-dodecyl group, n-1-lysosyl group, n-tetradecyl group, n-hexadecyl group, n-octadecyl group, n-
-icosyl group, tert-dodecyl group, tert-hexadecyl group (petroleum 5pirit)
It is a solvent based on

該鉱油は例えば、粘度が40°Cで46mm2/sであ
るパラフィン油のようなパラフィン油;”150ソルヘ
ント ヌートラル(SolventNeu tra l
) ”、粘度が40°Cで32mm2/sである精製溶
媒ヌートラル鉱油(solvent−refinedn
eutral m1neral oil)、および鉱油
精製過程から得られる高沸点性の残留分であり、粘度が
40°Cで46mm”/sである″ソルベント ブライ
トスドックス(Solvent Brightstoc
ks) ”であり得る。
The mineral oil is, for example, a paraffin oil such as paraffin oil with a viscosity of 46 mm2/s at 40°C;
)”, a refined solvent neutral mineral oil with a viscosity of 32 mm2/s at 40°C.
"Solvent Brightstox", which is a high-boiling residue obtained from the mineral oil refining process and has a viscosity of 46 mm"/s at 40°C.
ks)”.

芳香族炭化水素の媒体は例えば、トルエンまたは0−l
m−もしくはp−キシレン、トリメチルベンゼンまたは
ドデシルヘンゼンであり得る。
The aromatic hydrocarbon medium is, for example, toluene or 0-l
It can be m- or p-xylene, trimethylbenzene or dodecylhenzene.

脂肪族炭化水素の媒体は例えばn−デカンまたはn−ド
デカンである。
Aliphatic hydrocarbon media are, for example, n-decane or n-dodecane.

式Iの化合物は、有機媒体の全重量を基準にして有機媒
体中に好ましくは】、Oないし20重量%、更に好まし
くは2ないし15重量%の範囲の量で溶解されている。
The compound of formula I is preferably dissolved in the organic medium in an amount ranging from 0 to 20% by weight, more preferably from 2 to 15% by weight, based on the total weight of the organic medium.

式Iの化合物は既知の化合物であり、例えば英国特許2
172284Aに記載されている方法により製造され得
る。
The compounds of formula I are known compounds, e.g.
172284A.

この方法は、式V: (式中、Rは上述の意味を有する。)の化合物を製造す
るために式■: R−OH(I[[) (式中、Rは上述の意味を有する。)の化合物またはそ
の塩例えば、ナトリウム塩もしくはカリウム塩を、触媒
の不存在下または存在下、弐■: の化合物と反応させ; 次いで式Iの化合物を製造するために、式V類およびオ
キサゾリン類; C)燐含有化合物、例えば燐酸部分エステルのアミン塩
; d)硫黄含有化合物、例えばジノニルナフタレンスルボ
ン酸バリウムおよび石油スルポン酸カルシウム。
This process is used to prepare compounds of formula V: in which R has the meaning given above. ) or a salt thereof, such as a sodium salt or a potassium salt, in the absence or presence of a catalyst, with a compound of C) phosphorus-containing compounds, such as amine salts of phosphoric acid partial esters; d) sulfur-containing compounds, such as barium dinonylnaphthalene sulfonate and calcium petroleum sulfonate.

分散助剤/界面活性剤の例は: ポリブテニルコハク酸イミド、ポリブテニルホスホン酸
誘導体、およびスルホン酸の塩基性マグネシウム、カル
シウムおよびバリウム塩およびフェノールのマグネシウ
ム、カルシウムおよびバリウム塩。
Examples of dispersing aids/surfactants are: polybutenylsuccinimide, polybutenylphosphonic acid derivatives, and basic magnesium, calcium and barium salts of sulfonic acids and magnesium, calcium and barium salts of phenols.

〔実施例〕〔Example〕

下記の実施例は本発明を更に説明するものである。 The following examples further illustrate the invention.

1差1■」昌ニレ土 冷間圧延鉄鋼パネル(寸法:10102X152、厚み
二0.8価)を各々の試験溶液に数分間浸漬し、次いで
取り去り、そしてこのように処理されたパネルを排液す
るために約15時開放の化合物をジエクノールアミンと
反応させることを包含する。
1 Difference 1 ■'' Cold rolled steel panels (dimensions: 10102 x 152, thickness 20.8) were immersed in each test solution for several minutes, then removed, and the panels thus treated were drained. The process involves reacting the compound with diechnolamine at about 15 o'clock to obtain the reaction.

有機媒体は、弐Iの化合物に加えて、金属表面に一時的
保護を付与するのに有用であると知られている他の添加
剤、特に他の錆防止剤および分散助剤および/または界
面活性剤を含有してもよい。
The organic medium may contain, in addition to the compounds of Part 2, other additives known to be useful in imparting temporary protection to metal surfaces, in particular other rust inhibitors and dispersing aids and/or interfacial agents. It may also contain an activator.

錆防止剤の例は: a)有機酸、それらのエステル、金属塩および酸無水物
、例えばN−オレオイル ザルコシン、ソルビタン モ
ノ−オレエート、ナフテン酸鉛、無水ドデセニルコハク
酸、アルケニルコハク酸半エステル(haHester
)、4−ノニルフェノキシ酢酸; b)窒素含有化合物、例えば i)第1、第2もしくは第3脂肪族または環状脂肪族ア
ミンおよび有機酸と無機酸の該アミン塩、例えば油溶性
のアルキルアンモニウムカルボン酸塩類;および 11)複素環化合物、例えば置換イミダヅリン置する。
Examples of rust inhibitors are: a) organic acids, their esters, metal salts and acid anhydrides, such as N-oleoyl sarcosine, sorbitan mono-oleate, lead naphthenate, dodecenyl succinic anhydride, alkenyl succinic half esters (haHester
), 4-nonylphenoxyacetic acid; b) nitrogen-containing compounds, such as i) primary, secondary or tertiary aliphatic or cycloaliphatic amines and their amine salts of organic and inorganic acids, such as oil-soluble alkyl ammonium carbonates; and 11) heterocyclic compounds, such as substituted imidazurines.

次いで、各々の試験片をASTMB117に記述されて
いる方法に従って、24時間にわたって35°Cで5%
食塩水を連続的に散布するのに暴露させる。
Each specimen was then exposed to 5% at 35°C for 24 hours according to the method described in ASTM B117
Exposure to continuous saline spraying.

各々の試験溶液は、有a溶媒媒体として、下記の物理的
特性値を持つ石油塩基油を使用して製造された。
Each test solution was prepared using a petroleum base oil with the following physical properties as the solvent medium.

10.0    0.5    22.0      
3.7%CAは芳香族炭素含を量を意味する。
10.0 0.5 22.0
3.7% CA means aromatic carbon content.

2.4.6.8および24時間にわたり、食塩散布に暴
露した後、各々のパネルの錆の度合いを視覚的に検査し
、下記の尺度に従って評価された。
After exposure to the salt spray for 2.4.6.8 and 24 hours, each panel was visually inspected for degree of rust and rated according to the scale below.

錆を認められない。No rust detected.

パネルの20%が錆により被覆される。20% of the panel is covered with rust.

パネルの40%が錆により被覆される。40% of the panel is covered with rust.

パネルの60%が錆により被覆される。60% of the panel is covered with rust.

パネルの80%が錆により被覆される。80% of the panel is covered with rust.

パネルの100%が錆により被覆される。100% of the panel is covered with rust.

Claims (1)

【特許請求の範囲】 (1)式 I : R−O−CH_2−CH(OH)CH_2N(CH_2
CH_2OH)_2( I )〔式中、Rは炭素原子数1
2ないし20の直鎖のもしくは分枝したアルキル基、ま
たは式II:▲数式、化学式、表等があります▼(II) (式中、R^aは炭素原子数8ないし15の直鎖のもし
くは分枝したアルキル基を表し、そしててフェニル基の
3または4位に配置されている)を持つ基を表す〕を持
つ化合物の少なくとも一種を含有する無毒性の有機媒体
中に、保護されるべき金属表面を浸漬し、次いで該金属
表面を該媒体から取り去ることを包含する、腐食性大気
に接触している該金属表面に一時的な腐食防止保護を施
す方法。 (2)金属表面が鉄金属の表面である請求項(1)記載
の方法。 (3)Rがドデシル基、テトラデシル基、4−ノニルフ
ェニル基、4−ドデシルフェニル基または3−ペンタデ
シルフェニル基を表す請求項(1)記載の方法。 (4)有機媒体が鉱油、芳香族もしくは脂肪族炭化水素
または他のペトロリウムスピリット (petroleumspirit)を基材とする溶媒
である請求項(1)記載の方法。(5)有機媒体の重量
を基準にして1ないし20重量%の範囲の量で式 I の
化合物が該有機媒体中に存在する請求項(1)記載の方
法。 (6)有機媒体の重量を基準にして2ないし15重量%
の範囲の量で式 I の化合物が該有機媒体中に存在する
請求項(5)記載の方法。 (7)有機媒体が更に錆防止剤および/または分散助剤
および/または界面活性剤も含有する請求項(1)記載
の方法。 (8)請求項(1)記載の方法により一時的に保護され
ている時の金属表面。
[Claims] (1) Formula I: R-O-CH_2-CH(OH)CH_2N(CH_2
CH_2OH)_2(I) [wherein, R has 1 carbon atom]
2 to 20 straight chain or branched alkyl groups, or formula II: ▲ Numerical formula, chemical formula, table, etc. ▼ (II) (wherein R^a is a straight chain or branched alkyl group having 8 to 15 carbon atoms; represents a branched alkyl group and is located in the 3 or 4 position of the phenyl group. A method of providing temporary anti-corrosion protection to a metal surface in contact with a corrosive atmosphere, comprising immersing the metal surface and then removing the metal surface from the medium. (2) The method according to claim (1), wherein the metal surface is a surface of ferrous metal. (3) The method according to claim 1, wherein R represents a dodecyl group, a tetradecyl group, a 4-nonylphenyl group, a 4-dodecylphenyl group, or a 3-pentadecylphenyl group. (4) A method according to claim 1, wherein the organic medium is a mineral oil, aromatic or aliphatic hydrocarbon or other petroleum spirit based solvent. 5. A method according to claim 1, wherein the compound of formula I is present in the organic medium in an amount ranging from 1 to 20% by weight, based on the weight of the organic medium. (6) 2 to 15% by weight based on the weight of the organic medium;
A method according to claim 5, wherein the compound of formula I is present in the organic medium in an amount in the range of . (7) The method according to claim 1, wherein the organic medium further contains a rust inhibitor and/or a dispersion aid and/or a surfactant. (8) A metal surface when temporarily protected by the method according to claim (1).
JP2024997A 1989-02-03 1990-02-03 Protection Pending JPH02243785A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8902387A GB2227757B (en) 1989-02-03 1989-02-03 Protection method
GB8902387.3 1989-02-03

Publications (1)

Publication Number Publication Date
JPH02243785A true JPH02243785A (en) 1990-09-27

Family

ID=10651059

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2024997A Pending JPH02243785A (en) 1989-02-03 1990-02-03 Protection

Country Status (3)

Country Link
JP (1) JPH02243785A (en)
DE (1) DE4002826A1 (en)
GB (1) GB2227757B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102875394A (en) * 2012-10-16 2013-01-16 中国林业科学研究院林产化学工业研究所 Cashew nut phenol-amine polyalcohol and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102716693B (en) * 2012-06-26 2014-04-16 郑州大学 Cashew base nonionic surfactant and preparation method of cashew base nonionic surfactant

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2856363A (en) * 1955-12-01 1958-10-14 Pure Oil Co Stable anti-rust lubricating oil
GB2172284B (en) * 1985-03-12 1988-07-27 Ciba Geigy Ag Nitrogen-containing additives for non-aqueous functional fluids
EP0252007A3 (en) * 1986-06-28 1989-07-05 Ciba-Geigy Ag 2-propanol derivatives as corrosion inhibitors

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102875394A (en) * 2012-10-16 2013-01-16 中国林业科学研究院林产化学工业研究所 Cashew nut phenol-amine polyalcohol and preparation method thereof

Also Published As

Publication number Publication date
DE4002826A1 (en) 1990-08-09
GB2227757B (en) 1992-10-07
GB2227757A (en) 1990-08-08
GB8902387D0 (en) 1989-03-22

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