EP0295108A1 - Corrosion inhibiting composition - Google Patents
Corrosion inhibiting composition Download PDFInfo
- Publication number
- EP0295108A1 EP0295108A1 EP88305292A EP88305292A EP0295108A1 EP 0295108 A1 EP0295108 A1 EP 0295108A1 EP 88305292 A EP88305292 A EP 88305292A EP 88305292 A EP88305292 A EP 88305292A EP 0295108 A1 EP0295108 A1 EP 0295108A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition according
- metal
- carbon atoms
- composition
- corrosion inhibiting
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 76
- 238000005260 corrosion Methods 0.000 title claims abstract description 30
- 230000007797 corrosion Effects 0.000 title claims abstract description 26
- 230000002401 inhibitory effect Effects 0.000 title claims abstract description 21
- 229910052751 metal Chemical class 0.000 claims abstract description 41
- 239000002184 metal Chemical class 0.000 claims abstract description 41
- -1 basic metal sulfonate Chemical class 0.000 claims abstract description 31
- 150000003839 salts Chemical class 0.000 claims abstract description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 15
- 150000008064 anhydrides Chemical class 0.000 claims abstract description 10
- 229910052728 basic metal Inorganic materials 0.000 claims abstract description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 16
- 239000011575 calcium Substances 0.000 claims description 16
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 14
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical class OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 9
- 239000008199 coating composition Substances 0.000 claims description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
- 150000002739 metals Chemical class 0.000 claims description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 3
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 229940014800 succinic anhydride Drugs 0.000 claims description 3
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims description 2
- 239000012141 concentrate Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000001384 succinic acid Substances 0.000 claims description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
- 238000000576 coating method Methods 0.000 abstract description 14
- 125000002843 carboxylic acid group Chemical class 0.000 abstract description 2
- 230000007935 neutral effect Effects 0.000 description 12
- 229910052783 alkali metal Inorganic materials 0.000 description 9
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 239000002480 mineral oil Substances 0.000 description 8
- 235000010446 mineral oil Nutrition 0.000 description 8
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 5
- 150000001340 alkali metals Chemical class 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000003513 alkali Substances 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 2
- 238000003618 dip coating Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 235000011044 succinic acid Nutrition 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical class OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 150000003818 basic metals Chemical class 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 239000010720 hydraulic oil Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical group C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical group C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23F—NON-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
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/28—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M129/38—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
- C10M129/42—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms polycarboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
- C10M159/24—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing sulfonic radicals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
- C10M2207/127—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids polycarboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/22—Acids obtained from polymerised unsaturated acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/046—Overbasedsulfonic acid salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
Definitions
- This invention concerns corrosion inhibiting compositions which are useful as light duty or temporary corrosion preventatives and heavy duty or permanent corrosion preventatives.
- the invention relates to coatings which may be applied to metal for protection during storage between fabrication and use.
- coatings are generally applied from oil solution by spraying or dipping and must adhere to the metal sufficiently to give the desired anti-corrosion effect during the storage period which can be up to 6 months whilst at the same time being readily removable generally by washing with aqueous alkaline detergent to enable the metal to be painted. It is therefore important that the coatings have adequate light stability to ensure they are not converted to a laquer during storage which cannot then be easily removed.
- Corrosion inhibiting compositions based on alkali or alkaline earth metal salts are known.
- US Patent No. 3 453 124 relates to a product for inhibiting the corrosion of metal surfaces prepared by the reaction of (A) a non-Newtonian colloidal dispersed system comprising alkali or alkaline earth metal carbonates predispersed in dispersing medium and, as a third essential component, an alkali or alkaline earth metal salt of a carboxylic or sulphonic acid with (B) an acidic ester of a phosphoric acid.
- A a non-Newtonian colloidal dispersed system comprising alkali or alkaline earth metal carbonates predispersed in dispersing medium and, as a third essential component, an alkali or alkaline earth metal salt of a carboxylic or sulphonic acid with (B) an acidic ester of a phosphoric acid.
- US Patent No. 3 730 895 concerns greases thickened with conventional grease thickeners and containing a cloudy type overbased alkali metal or alkaline earth metal sulphonate or carboxylate dispersant and a water-soluble corrosion inhibiting salt, that is an alkali metal nitrite or an alkali metal chromate.
- US Patent No. 3 850 823 discloses a method for producing corrosion inhibiting compositions comprising lubricating oil, a cloudy type overbased alkali metal and/or alkaline earth metal dispersant and at least one water-soluble salt effective as a corrosion inhibitor, that is an alkali metal nitrite or an alkali metal chromate.
- US Patent No. 3 897 350 relates to anti-rust lubricating and hydraulic oil compositions containing a naphthtol, a metal sulphonate selected from neutral alkali metal sulphonate, neutral alkaline earth metal sulphonate, neutral zinc sulphonate, overbased alkali metal sulphonate, overbased alkaline earth metal sulphonate, and overbased zinc sulphonate, and a detergent selected from alkenyl succinimides, alkenyl succinic esters, alkyl lactone amides, alkyl lactam amides, and Mannich bases.
- PCT Application WO 86/03513 concerns corrosion inhibiting compositions comprising a mixture of (A) an oil-soluble neutral or basic alkali metal or alkaline earth metal salt or complex of an organic acid, and (B) a nitrogen- and boron- containing composition which is the reaction product of an amino alcohol, a boric acid or boron trioxide, and an organic carboxylic acid.
- US Patent No 3 714 042 discloses a composition prepared by a process comprising mixing (A) a basic metal complex selected from sulphonate, sulphonate-carboxylate and carboxylate complexes with up to an amount equivalent to the total basicity thereof of (B) a high molecular weight aliphatic carboxylic acid or anhydride wherein there are at least about 25 aliphatic carbon atoms per carboxy group in (B), such mixing is generally effected at temperatures that will cause the products to react.
- A a basic metal complex selected from sulphonate, sulphonate-carboxylate and carboxylate complexes with up to an amount equivalent to the total basicity thereof of (B) a high molecular weight aliphatic carboxylic acid or anhydride wherein there are at least about 25 aliphatic carbon atoms per carboxy group in (B), such mixing is generally effected at temperatures that will cause the products to react.
- Oxidation can be prevented or at least in large measure inhibited, by relatively impermeable coatings which have the effect of excluding moisture and/or oxygen from contact with the metal surface.
- coatings are often exposed to high humidity, corrosive atmosphere, etc, and to the extent that these coatings are penetrated or otherwise harmed by such influences they become ineffective for the desired purpose.
- a satisfactory corrosion-proof coating must have the ability to resist weathering, high humidity and corrosive atmospheres, such as air contaminated with industrial waste, so that a uniform protective film is maintained on all or most of the metal surface.
- a corrosion inhibiting composition comprises a mixture of (A) at least one basic metal sulphonate and (B) at least one aliphatic dicarboxylic acid or anhydride containing no more than 38 carbon atoms excluding the carbon atoms in the carboxylic acid or anhydride groups or a metal salt thereof.
- the metal salts of component (A) may be a group I or group II metal such as lithium, sodium, potassium, magnesium, calcium, strontium or barium.
- An alkaline earth metal and especially calcium is preferred, sodium salts are less preferred since their light resistance is inferior.
- Component (A) may be the salt of a natural or synthetic sulphonate and is preferably a metal salt of an alkyl substituted aromatic sulphonic acid.
- the product should have a residual basicity and we prefer it have a TBN of at least 40 preferably greater than 60. Blends of neutral and basic sulphonates may also be used.
- the sulphonic acid is a benzene sulphonic acid having 1-3 alkyl substituents in the meta and para positions of the benzene ring or a naphthalene sulphonic acid. Said alkyl substituents may be branched or linear or cyclic alkyl residues.
- At least one of said alkyl substituents of the benzene sulphonic acid is a "long-chain residue" containing from 12-50 carbon atoms.
- the additional alkyl substituents may also be long-chain residues or they may be short-chain residues containing less than 12 carbon atoms, for example, methyl or ethyl groups.
- Many processes have been described for the production of basic metal salts of such sulphonic acids and the choice of process is not important although the thixotiopic forms of the sulphonates, particularly calcium sulphonate, are not preferred since they can be difficult to remove from the metal.
- component (A) consists of a mixture of different alkyl benzene sulphonates which mainly differ in the size of their long-chain alkyl substituents. It is especially preferred that an even distribution of alkyl substituents continuously increasing in size is present in component (A). The substituents may increase in size over a range of 20 carbon atoms, especially from C10 to C30. Compositions according to this invention containing such mixtures of alkyl benzene sulphonates yield films on metal surfaces which are especially resistant to weathering and humidity.
- Component (B) is preferably an alkyl or alkenyl succinic acid or anhydride or a salt therefore preferred salts are the alkyl or alkenyl succinic acids or anhydrides containing from 6-32 aliphatic carbon atoms particularly those 10 to 24 especially 10 to 14 carbon atoms excluding those in the carboxylic acid groups or their salts.
- component (B) be present as the free acid or anhydride rather than the salt prior to application to the metal protected since it is believed that the presence of the free acid or anhydride can give improved adhesion to the metal.
- composition according to the present invention may further comprise a minor amount of a monocarboxylic metal salt, for example a formic acid salt.
- a monocarboxylic metal salt for example a formic acid salt.
- the mixture contains from 95% to 75% by weight of the basic metal sulphonate and from 5% to 25% by weight of the component B although the relative amounts will depend upon the use to which the composition is put. It is especially preferred that component (B) makes up 10-50 wt% of the total amount of components (A) and (B). It is preferred that the composition have residual basicity.
- the corrosion inhibiting compositions are employed as coating compositions which are solutions in a liquid vehicle.
- liquid vehicles are hydrocarbon oils and the various petroleum distillates which generally contain up to 15 wt% of the corrosion inhibiting composition, particularly up to 10 wt% generally between 0.5 and 5 wt% active ingredient content of the composition of the invention.
- the composition contains a non-polar vehicle there may additionally be present some metal in solid (colloidal) form associated with components (A) and (B) action as dispersants.
- the vehicle may also be a water-based system, for example a mixture of polyisobutylene, wax and water.
- the coating composition including the vehicle is usually grease-like material having a consistency from fluid to semi-solid.
- the corrosion inhibiting films of this invention may be applied to metal surfaces by any of the ordinary methods such as brushing, spraying, dip-coating, flow-coating, roller coating and the like.
- the viscosity of the corrosion inhibiting coating composition may be adjusted for the particular method of application selected by adding a suitable amount of diluent.
- the corrosion inhibiting compositions according to the present invention may be prepared in different ways, for example, by preparing the metal salts independently and mixing them subsequently. Alternatively a solution of an overbased metal sulphonate complex can be prepared to which an aliphatic dicarboxylic acid or its anhydride is added.
- the products are mixed in a manner that they do not react, i.e. the temperature is maintained below about 50°C although reaction products of components (A) and (B) are within the scope of the invention.
- the amount of the aliphatic dicarboxylic acid or its anhydride added to the overbased metal sulphonate complex should be such that the resulting mixture is overbased. Such overbased mixtures are also useful as corrosion inhibiting compositions.
- composition may be supplied as a concentrate preferably a solution of the mixture of (A) and (B) in oil in which case it is preferred that the solution contains from 20% to 60% active ingredient.
- the components may be supplied separately for incorporation into the final coating medium.
- the corrosion coatings of the present invention have improved weather resistance particularly resistance to light and can be readily removed from the metal to enable painting etc.
- the coatings may be used on metal sheets to be used for automobile manufacture, constructional steelwork in building and bridge building etc.
- compositions may also contain other additives such as antioxidants, antifoams, etc.
- additives such as antioxidants, antifoams, etc.
- the invention is further illustrated by the following examples.
- compositions according to the present invention and comparative compositions were prepared and their corrosion inhibiting effects were determined according to the methods of DIN 51 386 and DIN 50 017.
- Each cycle consisted of an eight hour period at a temperature of 40 ⁇ 3°C and a relative humidity of 100% followed by a 16 hour period at a temperature in the range of from 18-28°C and a relative humidity of less than 75%.
- compositions tested were based on mineral oil. They consisted of 94 wt.% mineral oil and 6 wt.% active ingredient (that is anything different from mineral oil). All compositions tested had a total base number in the range of from 6-10 milligram KOH/gram.
- a composition was prepared containing 94 wt.% of mineral oil (130 neutral base stock) and 6 wt.% of a mixture of calcium sulphonates.
- the calcium sulphonates employed were the neutral salt of 4-(C12-alkyl)-3,5-dimethyl benzene sulphonic acid and the basic salt of 4-(C24-alkyl) benzene sulphonic acid having a TOTAL BASE NUMBER (TBN) of 250 to give a blend of TBN 60 .
- TBN TOTAL BASE NUMBER
- a composition was prepared containing 94 wt.% of mineral oil (130 neutral base stock), 5.5 wt.% of a mixture of calcium sulphonates and 0.5 wt.% of solid calcium carbonate in colloidal form.
- the calcium sulphonates employed were salts of 4-(C12 -alkyl)-3,5-dimethyl benzene sulphonic acid, 4-(C18-alkyl) benzene sulphonic acid and 4-(C24-alkyl) benzene sulphonic acid of TBN 250 to provide the colloidal calcium carbonate.
- C12, C18 and C24 indicate the average number of carbon atoms in the long chain residue of the respective benzene sulphonic acid.
- a composition was prepared containing 94 wt.% of mineral oil (130 neutral base stock), 3.1 wt.% of a mixture of sodium sulphonates, 1.0 wt.% of a mixture of calcium sulphonates, and 1.9 wt.% of a calcium carboxylate.
- the sodium sulphonates employed were salts of 4-(C12 alkyl) -3,5-dimethyl benzene sulphonic acid and 4-(C24 alkyl) benzene sulphonic acid.
- the calcium sulphonates were the same as in Example 2.
- the calcium carboxylate was a salt prepared from an alkenyl succinic anhydride with an average number of 12 carbon atoms in the alkenyl residue.
- a composition was prepared containing 94 wt.% of mineral oil (130 neutral base stock), 4.0 wt.% of a mixture of calcium sulphonates used as in Example 3, and 2.0 wt.% of calcium carboxylate used in Example 4.
- Example 5 demonstrates the improved resistance to weathering and humidity of a composition according to the present invention.
- a comparison of Example 5 with Examples 2 and 3 shows the synergism between calcium sulphonates and calcium carboxylate.
- the products of the invention were compared with a similar composition containing the calcium salt of an C68 Alkenyl succinic acid, the products tested were prepared by adding the following formulations to oil (130 neutral base stock) to give the total active ingredient levels set out in Table 1.
- the formulations were tested as metal anti-corrosion coatings in the humidity cabinet (ASTM D 1748) and salt spray cabinet (ASTM B117) tests with the following results
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- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
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Abstract
- (A) at least one basic metal sulfonate and
- (B) at least one aliphatic dicarboxylic acid or anhydride containing no more than 38 carbon atoms excluding the carbon atoms in the carboxylic acid groups or a metal salt thereof
Description
- This invention concerns corrosion inhibiting compositions which are useful as light duty or temporary corrosion preventatives and heavy duty or permanent corrosion preventatives.
- In particular the invention relates to coatings which may be applied to metal for protection during storage between fabrication and use. Such coatings are generally applied from oil solution by spraying or dipping and must adhere to the metal sufficiently to give the desired anti-corrosion effect during the storage period which can be up to 6 months whilst at the same time being readily removable generally by washing with aqueous alkaline detergent to enable the metal to be painted. It is therefore important that the coatings have adequate light stability to ensure they are not converted to a laquer during storage which cannot then be easily removed.
- Corrosion inhibiting compositions based on alkali or alkaline earth metal salts are known.
- US Patent No. 3 453 124 relates to a product for inhibiting the corrosion of metal surfaces prepared by the reaction of (A) a non-Newtonian colloidal dispersed system comprising alkali or alkaline earth metal carbonates predispersed in dispersing medium and, as a third essential component, an alkali or alkaline earth metal salt of a carboxylic or sulphonic acid with (B) an acidic ester of a phosphoric acid.
- US Patent No. 3 730 895 concerns greases thickened with conventional grease thickeners and containing a cloudy type overbased alkali metal or alkaline earth metal sulphonate or carboxylate dispersant and a water-soluble corrosion inhibiting salt, that is an alkali metal nitrite or an alkali metal chromate.
- US Patent No. 3 850 823 discloses a method for producing corrosion inhibiting compositions comprising lubricating oil, a cloudy type overbased alkali metal and/or alkaline earth metal dispersant and at least one water-soluble salt effective as a corrosion inhibitor, that is an alkali metal nitrite or an alkali metal chromate.
- US Patent No. 3 897 350 relates to anti-rust lubricating and hydraulic oil compositions containing a naphthtol, a metal sulphonate selected from neutral alkali metal sulphonate, neutral alkaline earth metal sulphonate, neutral zinc sulphonate, overbased alkali metal sulphonate, overbased alkaline earth metal sulphonate, and overbased zinc sulphonate, and a detergent selected from alkenyl succinimides, alkenyl succinic esters, alkyl lactone amides, alkyl lactam amides, and Mannich bases.
- PCT Application WO 86/03513 concerns corrosion inhibiting compositions comprising a mixture of (A) an oil-soluble neutral or basic alkali metal or alkaline earth metal salt or complex of an organic acid, and (B) a nitrogen- and boron- containing composition which is the reaction product of an amino alcohol, a boric acid or boron trioxide, and an organic carboxylic acid.
- Mixture of basic sulphonates and naturally occurring unsaturated carboxylic acids such as linoleic acids are also used as temporary anti-corrosion coatings, these have poor light stability.
- It is known to treat overbased complexes with high molecular weight aliphatic carboxylic acids or acid derivatives.
- US Patent No 3 714 042 discloses a composition prepared by a process comprising mixing (A) a basic metal complex selected from sulphonate, sulphonate-carboxylate and carboxylate complexes with up to an amount equivalent to the total basicity thereof of (B) a high molecular weight aliphatic carboxylic acid or anhydride wherein there are at least about 25 aliphatic carbon atoms per carboxy group in (B), such mixing is generally effected at temperatures that will cause the products to react.
- It is generally assumed that the presence of both water and oxygen is essential for the oxidation of ferrous metal articles. Oxidation can be prevented or at least in large measure inhibited, by relatively impermeable coatings which have the effect of excluding moisture and/or oxygen from contact with the metal surface. Such coatings are often exposed to high humidity, corrosive atmosphere, etc, and to the extent that these coatings are penetrated or otherwise harmed by such influences they become ineffective for the desired purpose. A satisfactory corrosion-proof coating must have the ability to resist weathering, high humidity and corrosive atmospheres, such as air contaminated with industrial waste, so that a uniform protective film is maintained on all or most of the metal surface.
- It is an object of the present invention to provide corrosion inhibiting compositions for metals, especially ferrous metals, and a process for their preparation.
- It is also an object of the invention to provide corrosion inhibiting coating compositions for metals, which compositions are resistant to weathering including light stability and may be easily and inexpensively applied to metal surfaces and can also be readily removed to permit painting of the metal. It is a further object to provide metal coated with such corrosion inhibiting compositions.
- According to the present invention a corrosion inhibiting composition comprises a mixture of (A) at least one basic metal sulphonate and (B) at least one aliphatic dicarboxylic acid or anhydride containing no more than 38 carbon atoms excluding the carbon atoms in the carboxylic acid or anhydride groups or a metal salt thereof.
- Surprisingly the combination of basic metal sulphonate and aliphatic dicarboxylic acid and anhydride has a much stronger anti-corrosive effect than the basic metal sulphonate alone. Some sort of synergism between components (A) and (B) enhances the resistance to weathering and humidity of the protective film on the metal surface.
- The metal salts of component (A) may be a group I or group II metal such as lithium, sodium, potassium, magnesium, calcium, strontium or barium. An alkaline earth metal and especially calcium is preferred, sodium salts are less preferred since their light resistance is inferior.
- Component (A) may be the salt of a natural or synthetic sulphonate and is preferably a metal salt of an alkyl substituted aromatic sulphonic acid. The product should have a residual basicity and we prefer it have a TBN of at least 40 preferably greater than 60. Blends of neutral and basic sulphonates may also be used. Preferably the sulphonic acid is a benzene sulphonic acid having 1-3 alkyl substituents in the meta and para positions of the benzene ring or a naphthalene sulphonic acid. Said alkyl substituents may be branched or linear or cyclic alkyl residues. Preferably at least one of said alkyl substituents of the benzene sulphonic acid is a "long-chain residue" containing from 12-50 carbon atoms. The additional alkyl substituents may also be long-chain residues or they may be short-chain residues containing less than 12 carbon atoms, for example, methyl or ethyl groups. Many processes have been described for the production of basic metal salts of such sulphonic acids and the choice of process is not important although the thixotiopic forms of the sulphonates, particularly calcium sulphonate, are not preferred since they can be difficult to remove from the metal.
- Preferably component (A) consists of a mixture of different alkyl benzene sulphonates which mainly differ in the size of their long-chain alkyl substituents. It is especially preferred that an even distribution of alkyl substituents continuously increasing in size is present in component (A). The substituents may increase in size over a range of 20 carbon atoms, especially from C₁₀ to C₃₀. Compositions according to this invention containing such mixtures of alkyl benzene sulphonates yield films on metal surfaces which are especially resistant to weathering and humidity.
- Component (B) is preferably an alkyl or alkenyl succinic acid or anhydride or a salt therefore preferred salts are the alkyl or alkenyl succinic acids or anhydrides containing from 6-32 aliphatic carbon atoms particularly those 10 to 24 especially 10 to 14 carbon atoms excluding those in the carboxylic acid groups or their salts.
- It is preferred that the component (B) be present as the free acid or anhydride rather than the salt prior to application to the metal protected since it is believed that the presence of the free acid or anhydride can give improved adhesion to the metal.
- The composition according to the present invention may further comprise a minor amount of a monocarboxylic metal salt, for example a formic acid salt.
- It is preferred that the mixture contains from 95% to 75% by weight of the basic metal sulphonate and from 5% to 25% by weight of the component B although the relative amounts will depend upon the use to which the composition is put. It is especially preferred that component (B) makes up 10-50 wt% of the total amount of components (A) and (B). It is preferred that the composition have residual basicity.
- Usually the corrosion inhibiting compositions are employed as coating compositions which are solutions in a liquid vehicle. Examples of liquid vehicles are hydrocarbon oils and the various petroleum distillates which generally contain up to 15 wt% of the corrosion inhibiting composition, particularly up to 10 wt% generally between 0.5 and 5 wt% active ingredient content of the composition of the invention. If the composition contains a non-polar vehicle there may additionally be present some metal in solid (colloidal) form associated with components (A) and (B) action as dispersants.
- The vehicle may also be a water-based system, for example a mixture of polyisobutylene, wax and water.
- The coating composition including the vehicle is usually grease-like material having a consistency from fluid to semi-solid. The corrosion inhibiting films of this invention may be applied to metal surfaces by any of the ordinary methods such as brushing, spraying, dip-coating, flow-coating, roller coating and the like. The viscosity of the corrosion inhibiting coating composition may be adjusted for the particular method of application selected by adding a suitable amount of diluent.
- The corrosion inhibiting compositions according to the present invention may be prepared in different ways, for example, by preparing the metal salts independently and mixing them subsequently. Alternatively a solution of an overbased metal sulphonate complex can be prepared to which an aliphatic dicarboxylic acid or its anhydride is added.
- It is preferred that the products are mixed in a manner that they do not react, i.e. the temperature is maintained below about 50°C although reaction products of components (A) and (B) are within the scope of the invention. The amount of the aliphatic dicarboxylic acid or its anhydride added to the overbased metal sulphonate complex should be such that the resulting mixture is overbased. Such overbased mixtures are also useful as corrosion inhibiting compositions.
- The composition may be supplied as a concentrate preferably a solution of the mixture of (A) and (B) in oil in which case it is preferred that the solution contains from 20% to 60% active ingredient. Alternatively the components may be supplied separately for incorporation into the final coating medium.
- We have found that the corrosion coatings of the present invention have improved weather resistance particularly resistance to light and can be readily removed from the metal to enable painting etc. The coatings may be used on metal sheets to be used for automobile manufacture, constructional steelwork in building and bridge building etc.
- The compositions may also contain other additives such as antioxidants, antifoams, etc. The invention is further illustrated by the following examples.
- Compositions according to the present invention and comparative compositions were prepared and their corrosion inhibiting effects were determined according to the methods of DIN 51 386 and DIN 50 017.
- Steel panels of identical size were washed, rinsed, and dried. The dry panels were coated with the respective composition by dip coating. The coated panels were then stored in a climatic chamber.
- The climate in the chamber was varied in cycles. Each cycle consisted of an eight hour period at a temperature of 40 ± 3°C and a relative humidity of 100% followed by a 16 hour period at a temperature in the range of from 18-28°C and a relative humidity of less than 75%.
- It was determined how many cycles could be run before the first rust spot appeared on the panel. A larger number of cycles indicates a better anti-corrosion performance of the product tested.
- Each composition was tested on two steel panels. The numbers given for each composition in Examples 1 to 5 are the average of two tests.
- All compositions tested were based on mineral oil. They consisted of 94 wt.% mineral oil and 6 wt.% active ingredient (that is anything different from mineral oil). All compositions tested had a total base number in the range of from 6-10 milligram KOH/gram.
- The corrosion inhibiting performance of a mineral oil (130 neutral base stock) without active ingredient was tested. The number of cycles before appearance of the first rust spot was 0.
- A composition was prepared containing 94 wt.% of mineral oil (130 neutral base stock) and 6 wt.% of a mixture of calcium sulphonates. The calcium sulphonates employed were the neutral salt of 4-(C₁₂-alkyl)-3,5-dimethyl benzene sulphonic acid and the basic salt of 4-(C₂₄-alkyl) benzene sulphonic acid having a TOTAL BASE NUMBER (TBN) of 250 to give a blend of TBN 60 . C₁₂ and C₂₄ indicate the average number of carbon atoms in the long-chain residue of the respective benzene sulphonic acid.
- Steel panels coated with this composition were tested in the climatic chamber. The number of cycles before appearance of the first rust spot was 13.
- A composition was prepared containing 94 wt.% of mineral oil (130 neutral base stock), 5.5 wt.% of a mixture of calcium sulphonates and 0.5 wt.% of solid calcium carbonate in colloidal form. The calcium sulphonates employed were salts of 4-(C₁₂ -alkyl)-3,5-dimethyl benzene sulphonic acid, 4-(C₁₈-alkyl) benzene sulphonic acid and 4-(C₂₄-alkyl) benzene sulphonic acid of TBN 250 to provide the colloidal calcium carbonate. C₁₂, C₁₈ and C₂₄ indicate the average number of carbon atoms in the long chain residue of the respective benzene sulphonic acid.
- Steel panels coated with this composition were tested in the climatic chamber. The number of cycles before appearance of the first rust spot was 15.
- A composition was prepared containing 94 wt.% of mineral oil (130 neutral base stock), 3.1 wt.% of a mixture of sodium sulphonates, 1.0 wt.% of a mixture of calcium sulphonates, and 1.9 wt.% of a calcium carboxylate. The sodium sulphonates employed were salts of 4-(C₁₂ alkyl) -3,5-dimethyl benzene sulphonic acid and 4-(C₂₄ alkyl) benzene sulphonic acid. The calcium sulphonates were the same as in Example 2. The calcium carboxylate was a salt prepared from an alkenyl succinic anhydride with an average number of 12 carbon atoms in the alkenyl residue.
- Steel panels coated with this composition were tested in the climatic chamber. The number of cycles before appearance of the first rust spot was 25.
- A composition was prepared containing 94 wt.% of mineral oil (130 neutral base stock), 4.0 wt.% of a mixture of calcium sulphonates used as in Example 3, and 2.0 wt.% of calcium carboxylate used in Example 4.
- Steel panels coated with this composition were tested in the climatic chamber. The number of cycles before appearance of the first rust spot was 30.
- This Example demonstrates the improved resistance to weathering and humidity of a composition according to the present invention. A comparison of Example 5 with Examples 2 and 3 shows the synergism between calcium sulphonates and calcium carboxylate.
- The products of the invention were compared with a similar composition containing the calcium salt of an C68 Alkenyl succinic acid, the products tested were prepared by adding the following formulations to oil (130 neutral base stock) to give the total active ingredient levels set out in Table 1. The formulations were tested as metal anti-corrosion coatings in the humidity cabinet (ASTM D 1748) and salt spray cabinet (ASTM B117) tests with the following results
Claims (14)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT88305292T ATE65554T1 (en) | 1987-06-10 | 1988-06-09 | CORROSION INHIBITOR COMPOSITION. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB878713549A GB8713549D0 (en) | 1987-06-10 | 1987-06-10 | Corrosion inhibiting composition |
GB8713549 | 1987-06-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0295108A1 true EP0295108A1 (en) | 1988-12-14 |
EP0295108B1 EP0295108B1 (en) | 1991-07-24 |
Family
ID=10618674
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88305292A Expired - Lifetime EP0295108B1 (en) | 1987-06-10 | 1988-06-09 | Corrosion inhibiting composition |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0295108B1 (en) |
JP (1) | JP2728708B2 (en) |
AT (1) | ATE65554T1 (en) |
DE (1) | DE3863848D1 (en) |
ES (1) | ES2024024B3 (en) |
GB (1) | GB8713549D0 (en) |
WO (1) | WO1988009831A1 (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0393732A2 (en) * | 1989-04-21 | 1990-10-24 | King Industries, Inc. | Thermooxidatively stable compositions |
EP0413859A1 (en) * | 1988-08-18 | 1991-02-27 | Exxon Chemical Patents Inc. | Metal protecting compositions |
EP0414967A1 (en) * | 1989-08-21 | 1991-03-06 | Exxon Chemical Patents Inc. | Coating compositions |
EP0421250A2 (en) * | 1989-10-02 | 1991-04-10 | Ppg Industries, Inc. | Protective coating composition |
US5133900A (en) * | 1987-03-16 | 1992-07-28 | King Industries, Inc. | Thermooxidatively stable compositions |
US5169564A (en) * | 1987-03-16 | 1992-12-08 | King Industries, Inc. | Thermooxidatively stable compositions |
US5244957A (en) * | 1989-08-17 | 1993-09-14 | Exxon Chemical Patents Inc. | Metal protecting compositions |
WO1998016668A1 (en) * | 1996-10-15 | 1998-04-23 | N.V. Bekaert S.A. | Elongated steel object treated with a corrosion inhibiting composition |
EP0848054A1 (en) * | 1996-12-11 | 1998-06-17 | Idemitsu Kosan Company Limited | Metal working oil composition |
US6699822B2 (en) | 2002-06-07 | 2004-03-02 | Georgia-Pacific Resin, Inc. | Sulfated dicarboxylic acids for lubrication, emulsification, and corrosion inhibition |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4229848A1 (en) * | 1992-09-07 | 1994-03-10 | Henkel Kgaa | Amine-free cooling lubricants |
CN115335495B (en) * | 2020-03-12 | 2024-05-31 | 路博润公司 | Oil-based corrosion inhibitors |
CN113249162A (en) * | 2021-05-24 | 2021-08-13 | 新乡市瑞丰新材料股份有限公司 | Preparation method of composite calcium sulfonate antirust agent |
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US3453124A (en) * | 1963-08-07 | 1969-07-01 | Lubrizol Corp | Corrosion inhibiting composition |
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GB2131444A (en) * | 1982-06-22 | 1984-06-20 | Dai Ichi Kogyo Seiyaku Co Ltd | Aqueous emulsion type rust inhibitor |
-
1987
- 1987-06-10 GB GB878713549A patent/GB8713549D0/en active Pending
-
1988
- 1988-06-09 ES ES88305292T patent/ES2024024B3/en not_active Expired - Lifetime
- 1988-06-09 DE DE8888305292T patent/DE3863848D1/en not_active Expired - Lifetime
- 1988-06-09 AT AT88305292T patent/ATE65554T1/en not_active IP Right Cessation
- 1988-06-09 EP EP88305292A patent/EP0295108B1/en not_active Expired - Lifetime
- 1988-06-10 WO PCT/GB1988/000450 patent/WO1988009831A1/en unknown
- 1988-06-10 JP JP63504723A patent/JP2728708B2/en not_active Expired - Fee Related
Patent Citations (7)
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US3004917A (en) * | 1959-05-14 | 1961-10-17 | Exxon Research Engineering Co | Oil compositions containing rust inhibitors |
US3453124A (en) * | 1963-08-07 | 1969-07-01 | Lubrizol Corp | Corrosion inhibiting composition |
US3422013A (en) * | 1967-07-07 | 1969-01-14 | Lubrizol Corp | Process for the preparation of non-newtonian colloidal disperse systems |
GB1265969A (en) * | 1967-12-23 | 1972-03-08 | ||
US3714042A (en) * | 1969-03-27 | 1973-01-30 | Lubrizol Corp | Treated overbased complexes |
US3897350A (en) * | 1974-05-30 | 1975-07-29 | Mobil Oil Corp | Anti-rust compositions |
GB2131444A (en) * | 1982-06-22 | 1984-06-20 | Dai Ichi Kogyo Seiyaku Co Ltd | Aqueous emulsion type rust inhibitor |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5133900A (en) * | 1987-03-16 | 1992-07-28 | King Industries, Inc. | Thermooxidatively stable compositions |
US5169564A (en) * | 1987-03-16 | 1992-12-08 | King Industries, Inc. | Thermooxidatively stable compositions |
EP0413859A1 (en) * | 1988-08-18 | 1991-02-27 | Exxon Chemical Patents Inc. | Metal protecting compositions |
EP0393732A3 (en) * | 1989-04-21 | 1991-01-09 | King Industries, Inc. | Thermooxidatively stable compositions |
EP0393732A2 (en) * | 1989-04-21 | 1990-10-24 | King Industries, Inc. | Thermooxidatively stable compositions |
US5244957A (en) * | 1989-08-17 | 1993-09-14 | Exxon Chemical Patents Inc. | Metal protecting compositions |
EP0414967A1 (en) * | 1989-08-21 | 1991-03-06 | Exxon Chemical Patents Inc. | Coating compositions |
EP0421250A3 (en) * | 1989-10-02 | 1992-05-13 | Ppg Industries, Inc. | Protective coating composition |
EP0421250A2 (en) * | 1989-10-02 | 1991-04-10 | Ppg Industries, Inc. | Protective coating composition |
WO1998016668A1 (en) * | 1996-10-15 | 1998-04-23 | N.V. Bekaert S.A. | Elongated steel object treated with a corrosion inhibiting composition |
US6329073B1 (en) | 1996-10-15 | 2001-12-11 | N.V. Bekaert S.A. | Elongated steel object treated with a corrosion inhibiting composition |
EP0848054A1 (en) * | 1996-12-11 | 1998-06-17 | Idemitsu Kosan Company Limited | Metal working oil composition |
US5908816A (en) * | 1996-12-11 | 1999-06-01 | Idemitsu Kosan Co., Ltd. | Metal working oil composition |
US6699822B2 (en) | 2002-06-07 | 2004-03-02 | Georgia-Pacific Resin, Inc. | Sulfated dicarboxylic acids for lubrication, emulsification, and corrosion inhibition |
Also Published As
Publication number | Publication date |
---|---|
ES2024024B3 (en) | 1992-02-16 |
JPH02501315A (en) | 1990-05-10 |
JP2728708B2 (en) | 1998-03-18 |
WO1988009831A1 (en) | 1988-12-15 |
EP0295108B1 (en) | 1991-07-24 |
ATE65554T1 (en) | 1991-08-15 |
GB8713549D0 (en) | 1987-07-15 |
DE3863848D1 (en) | 1991-08-29 |
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