US3267038A - Inhibiting the corrosion of coppercontaining metals - Google Patents
Inhibiting the corrosion of coppercontaining metals Download PDFInfo
- Publication number
- US3267038A US3267038A US209770A US20977062A US3267038A US 3267038 A US3267038 A US 3267038A US 209770 A US209770 A US 209770A US 20977062 A US20977062 A US 20977062A US 3267038 A US3267038 A US 3267038A
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- Prior art keywords
- sodium
- acids
- corrosion
- acid
- dimer
- 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 - Lifetime
Links
- 238000005260 corrosion Methods 0.000 title description 21
- 230000007797 corrosion Effects 0.000 title description 21
- 230000002401 inhibitory effect Effects 0.000 title description 11
- 229910052751 metal Inorganic materials 0.000 title description 7
- 239000002184 metal Substances 0.000 title description 7
- 150000002739 metals Chemical class 0.000 title description 5
- 239000002253 acid Substances 0.000 claims description 41
- 239000003599 detergent Substances 0.000 claims description 34
- 150000007513 acids Chemical class 0.000 claims description 31
- 239000000203 mixture Substances 0.000 claims description 22
- 229920000388 Polyphosphate Polymers 0.000 claims description 16
- 239000001205 polyphosphate Substances 0.000 claims description 16
- 235000011176 polyphosphates Nutrition 0.000 claims description 16
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 claims description 14
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 12
- 229910052708 sodium Inorganic materials 0.000 claims description 9
- 239000011734 sodium Substances 0.000 claims description 9
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 claims description 9
- 229940048086 sodium pyrophosphate Drugs 0.000 claims description 9
- 235000019818 tetrasodium diphosphate Nutrition 0.000 claims description 9
- 239000000178 monomer Substances 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- 150000001340 alkali metals Chemical class 0.000 claims description 5
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 claims description 5
- 235000019982 sodium hexametaphosphate Nutrition 0.000 claims description 5
- 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 claims description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 238000005649 metathesis reaction Methods 0.000 claims description 2
- 239000000539 dimer Substances 0.000 description 25
- 229910000881 Cu alloy Inorganic materials 0.000 description 17
- 238000000034 method Methods 0.000 description 14
- 239000000243 solution Substances 0.000 description 14
- -1 bicyclic aromatic dicarboxylic acids Chemical class 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 8
- 239000003112 inhibitor Substances 0.000 description 7
- 229910001369 Brass Inorganic materials 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
- 239000010951 brass Substances 0.000 description 6
- 229910052938 sodium sulfate Inorganic materials 0.000 description 6
- 235000011152 sodium sulphate Nutrition 0.000 description 6
- 229910000906 Bronze Inorganic materials 0.000 description 4
- 239000010974 bronze Substances 0.000 description 4
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 4
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 235000011180 diphosphates Nutrition 0.000 description 3
- 229940005740 hexametaphosphate Drugs 0.000 description 3
- 235000020778 linoleic acid Nutrition 0.000 description 3
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 3
- 150000002763 monocarboxylic acids Chemical class 0.000 description 3
- 125000002950 monocyclic group Chemical group 0.000 description 3
- 229940048084 pyrophosphate Drugs 0.000 description 3
- JHJUUEHSAZXEEO-UHFFFAOYSA-M sodium;4-dodecylbenzenesulfonate Chemical group [Na+].CCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 JHJUUEHSAZXEEO-UHFFFAOYSA-M 0.000 description 3
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 2
- 229910000554 Admiralty brass Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- AZSFNUJOCKMOGB-UHFFFAOYSA-K cyclotriphosphate(3-) Chemical class [O-]P1(=O)OP([O-])(=O)OP([O-])(=O)O1 AZSFNUJOCKMOGB-UHFFFAOYSA-K 0.000 description 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- TVZISJTYELEYPI-UHFFFAOYSA-N hypodiphosphoric acid Chemical compound OP(O)(=O)P(O)(O)=O TVZISJTYELEYPI-UHFFFAOYSA-N 0.000 description 2
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- ZUUFLXSNVWQOJW-MBIXAETLSA-N (2e,4e,6e)-octadeca-2,4,6-trienoic acid Chemical compound CCCCCCCCCCC\C=C\C=C\C=C\C(O)=O ZUUFLXSNVWQOJW-MBIXAETLSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- KYXHKHDZJSDWEF-LHLOQNFPSA-N CCCCCCC1=C(CCCCCC)C(\C=C\CCCCCCCC(O)=O)C(CCCCCCCC(O)=O)CC1 Chemical compound CCCCCCC1=C(CCCCCC)C(\C=C\CCCCCCCC(O)=O)C(CCCCCCCC(O)=O)CC1 KYXHKHDZJSDWEF-LHLOQNFPSA-N 0.000 description 1
- 241001517013 Calidris pugnax Species 0.000 description 1
- 229910000776 Common brass Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000570 Cupronickel Inorganic materials 0.000 description 1
- 229910000562 Gilding metal Inorganic materials 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229910000936 Naval brass Inorganic materials 0.000 description 1
- 241001275902 Parabramis pekinensis Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 1
- VJZWIFWPGRIJSN-XRHABHTOSA-N dilinoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O VJZWIFWPGRIJSN-XRHABHTOSA-N 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- UWZUWNMEIDBHOF-DPMBMXLASA-M lithium;(z,12r)-12-hydroxyoctadec-9-enoate Chemical compound [Li+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O UWZUWNMEIDBHOF-DPMBMXLASA-M 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- C23F11/12—Oxygen-containing compounds
- C23F11/124—Carboxylic acids
- C23F11/126—Aliphatic acids
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
Definitions
- This invention relates to a method for inhibiting corrosive attack upon copper alloys contacted by aerated, aqueous detergent solutions, and to a novel detergent composition.
- Copper alloys such as brasses and bronzes usually display high resistance to corrosive attack by water or aerated, aqueous, salt solutions. Copper alloys which are highly resistant to corrosive attack, such as admiralty brass, nevertheless have been found to be rapidly corroded when contacted by aerated, aqueous solutions of commercial detergents.
- the art recognizes numerous organic compounds which can be used to inhibit the corrosion of metals subject to corrosive attack by aerated, aqueous solutions. Such inhibitors have been found to be generally ineffective, or only slightly effective, for inhibiting the corrosion of copper alloys contacted by aerated, aqueous solutions of commercial detergents.
- the dimer acids useful in this invention have been produced by heat polymerization of esters of monocarboxylic acids to esters of the dimer acids, followed by hydrolysis. Numerous examples of the dimer acids useful in the method of this invention, and the methods of preparation of such dimer acids, are described in detail in US. Patents Nos. 2,482,761 and 2,763,612.
- the dimer acids useful in the method of this invention are monocyclic or bicyclic aromatic dicarboxylic acids, depending upon the degree of unsaturation of the monocarboxylic acids from which the dimer acids are obtained.
- octadecadienoic acids polymerize to monocyclic dicarboxylic acids
- octadecatrienoic acids polymerize to bicyclic dicarboxylic acids.
- the cyclic dimerized acids are derivable from polyolefinic, monocarboxylic fatty acid monomers having at least carbon atoms per molecule.
- dimer acids when used in the amount of about 0.005 to 0.1 percent by weight, in aerated aqueous solutions of commercial detergents containing polyphosphate builders, are effective for inhibiting the corrosion of copper alloys contacted by such solutions.
- R is CH (CH R is (CH COOH, n is one more than the number of CH groups between the terminal CH group and the near carbon atom of the near double bond, and m is the number of CH groups between the carboxylic group of the monocarboxylic acid and the near carbon of the near double bond.
- Typical of the diethenoid acids capable of dimerization in accordance with this invention is the diethenoid linoleic acid, or A -octadecadienoic acid. This acid dimerizes in the absence of other polyethenoid acids to form the monocyclic dimeric dicarboxylic acid in which R is CH (CH and R is (CH COOH.
- the dimeric acids obtained are bicyclic dicarboxylic acids having a formula such as:
- bicyclic dicarboxylic dimer acid-forming monomers when only a single acid undergoes polymerization.
- Typical of the bicyclic dicarboxylic dimer acid-forming monomers is the triethenoid linolenic acid, or A octadecatrienoic acid. When this is the sole polyethenoid acid present it polymerizes to form the dimer carboxylic acid of the foregoing formula.
- the method of this invention is useful in protecting numerous copper alloys from corrosive attack by aerated aqueous solutions of commercial detergents containing effective amounts of polyphosphate builders.
- Copper alloys, having normally high corrosion resistance, which are readily attacked by aqueous, aerated, polyphosphate solutions include copper-zinc alloys containing 6090% by weight of copper, such as gilding metal, commercial bronze, red brass, spring brass, common brass, Muntz metals, and admiralty brass.
- Copper alloys containing minor amounts of metal such as zinc, lead, tin, aluminum, and nickel, such as forging brass, architectural bronze, aluminum brass, naval brass, nickel-aluminum bronze, aluminum bronze, and cupro-nickel, are also subject to corrosive attack and can be inhibited in accordance with this invention.
- the alloys protected can also contain minor amounts of manganese, beryllium or phosphorus.
- alkali-metal polyphosphate salts responsible for accelerated corrosive attack upon normally corrosion-resistant copper alloys are the pyrophosphate, tripolyphosphate, hypophosphate, hexametaphosphate, and trimetaphosphate salts.
- the pyrophosphate, tripolyphosphate, and hexametaphosphate salts of sodium are especially likely to be found in commercial detergents, and result in serious corrosion problems when such detergents are employed in apparatus fabricated of copper alloys.
- dimer acids were not as effective in inhibiting corrosive attack upon copper alloys induced by the synthetic detergent compositions of Table II. This is believed to be because of the abnormally high concentration of polyphosphates in the compositions of Table II. In these experiments, the same procedures as described with reference to Table I were employed.
- This invention also contemplates and includes detergent compositions per se which employ polyphosphate builders and which include a small but effective amount of dimer acids to inhibit corrosion of copper alloys which would otherwise occur when the detergent is placed in aqueous solution and contacts structures fabricated of copper alloys.
- the detergent compositions of this invention will include any of a wide variety of cationic, nonionic, or anionic detergents which include a minor but effective amount of polyphosphate builders, and a small amount of dimer acid inhibitor.
- compositions are detergents based upon alkaryl sodium sulfonates, and including minor amounts, usually in the range of about 5-20%, of polyphosphate builders such as the alkali-metal pyrophosphate, tripolyphosphate, hexametaphosphate, trimetaphosphate, and hypophosphate salts. More preferably, the builders will be the solium salts such as sodium pyrophosphate, sodium tripolyphosphate, and sodium hexametaphosphate.
- a preferred detergent base is dodecylbenzene sodium sulfonate.
- the detergent composition will contain about 120% by weight, and preferably about 5% by weight, based upon the total weight of the detergent composition, of the aforedefined dimer acid.
- a specific example of a detergent composition in accordance with this invention is as follows:
- a composition consisting essentially of an alkaryl sodium sulfonate detergent, alkali-metal polyphosphate salts selected from the group consisting of sodium pyrophosphate, sodium tripolyphosphate, and sodium hexametaphosphate in an amount sufficient to inhibit metathesis aud about 120% by weight of the total composition of cyclic, dimerized acids having at least two olefinic linkages per molecule and being derivable from polyolefinic, monocarboxylic fatty acid monomers having at least carbon atoms per molecule.
- composition in accordance with claim 1 in which said detergent includes a major proportion of alkaryl sodium sulfonates.
- composition in accordance with claim 2 in which said sulfonate is dodecylbenzene sodium sulfonate.
- composition in accordance with claim 3 in which said dimeric acid is a dimer of A -octadecadienoic acid.
- alkali-metal polyphosphate salts selected from the group consisting of sodium pyrophosphate, sodium tripolyphosphate, and sodium hexametaphosphate in amounts suflicient to promote corrosion of said copper- 6 containing metals
- the improvement consisting essentially of adding to the solutions about 0.005 to 0.1%, by Weight of said solution, of cyclic dimerized acids having at least two olefinic linkages per molecule and being derivable from polyolefinic monocarboxylic fatty acid monomers having at least 10 carbon atoms per molecule.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Detergent Compositions (AREA)
Description
United States This invention relates to a method for inhibiting corrosive attack upon copper alloys contacted by aerated, aqueous detergent solutions, and to a novel detergent composition.
Copper alloys such as brasses and bronzes usually display high resistance to corrosive attack by water or aerated, aqueous, salt solutions. Copper alloys which are highly resistant to corrosive attack, such as admiralty brass, nevertheless have been found to be rapidly corroded when contacted by aerated, aqueous solutions of commercial detergents. The art recognizes numerous organic compounds which can be used to inhibit the corrosion of metals subject to corrosive attack by aerated, aqueous solutions. Such inhibitors have been found to be generally ineffective, or only slightly effective, for inhibiting the corrosion of copper alloys contacted by aerated, aqueous solutions of commercial detergents.
It has been determined that this condition is due to the presence of builders in detergent formulations, these builders being alkali-metal polyphosphate salts, commonly sodium tripolyphosphate, sodium pyrophosphate, or sodium hexametaphosphate, or mixtures thereof. Normally, in the use of detergent compositions in machinery such as found in laundries or factories, coatings of corrosion products and other insolubles form a protective layer on metal surfaces. The presence of builders in detergents, however, prevents or removes this layer and promotes corrosion of the metallic surfaces. It has been found that such corrosion can be effectively inhibited by incorporating in the aqueous medium small amounts of certain dimer acids.
It is therefore an object of this invention to provide a novel method for inhibiting the corrosion of copper alloys contacted by aerated, aqueous, detergent solutions. Another object of this invention is to provide a novel detergent composition for use in apparatus fabricated at least in part of copper alloys. Other objects of this invention will become apparent from the following description.
In general, the dimer acids useful in this invention have been produced by heat polymerization of esters of monocarboxylic acids to esters of the dimer acids, followed by hydrolysis. Numerous examples of the dimer acids useful in the method of this invention, and the methods of preparation of such dimer acids, are described in detail in US. Patents Nos. 2,482,761 and 2,763,612. The dimer acids useful in the method of this invention are monocyclic or bicyclic aromatic dicarboxylic acids, depending upon the degree of unsaturation of the monocarboxylic acids from which the dimer acids are obtained. Thus, octadecadienoic acids polymerize to monocyclic dicarboxylic acids, while octadecatrienoic acids polymerize to bicyclic dicarboxylic acids. The cyclic dimerized acids are derivable from polyolefinic, monocarboxylic fatty acid monomers having at least carbon atoms per molecule. Such dimer acids, when used in the amount of about 0.005 to 0.1 percent by weight, in aerated aqueous solutions of commercial detergents containing polyphosphate builders, are effective for inhibiting the corrosion of copper alloys contacted by such solutions.
atent 3,267,038 Patented August 16, 1966 where R is CH (CH R is (CH COOH, n is one more than the number of CH groups between the terminal CH group and the near carbon atom of the near double bond, and m is the number of CH groups between the carboxylic group of the monocarboxylic acid and the near carbon of the near double bond.
Typical of the diethenoid acids capable of dimerization in accordance with this invention is the diethenoid linoleic acid, or A -octadecadienoic acid. This acid dimerizes in the absence of other polyethenoid acids to form the monocyclic dimeric dicarboxylic acid in which R is CH (CH and R is (CH COOH.
When triand greater ethenoid acids such as n-linolenic acids are dimerized, the dimeric acids obtained are bicyclic dicarboxylic acids having a formula such as:
when only a single acid undergoes polymerization. Typical of the bicyclic dicarboxylic dimer acid-forming monomers is the triethenoid linolenic acid, or A octadecatrienoic acid. When this is the sole polyethenoid acid present it polymerizes to form the dimer carboxylic acid of the foregoing formula.
A well-known source of these dimeric acids is the product sold by Emery Industries, Incorporated, and said to be a dilinoleic acid. The properties of these materials are as follows:
Neutral equivalent 290-310 Iodine value 95 Color Gardner 12 Dimer content, percent About Trimer and higher content, percent About 12 Monomer content, percent About 3 It will be noted that the dimeric acids as commercially produced contain about 85% dimeric acids and 12% trimeric and higher polymeric acids. Since the dimeric acids are not available in pure form, the experiments reported in this specification were conducted employing commercially available dimeric acids of about 85% purity. While the use of commercial products of 85% purity has proved to be highly satisfactory, it is expected that still better inhibition can be obtained with pure dimer acids. Especially preferred are the monocy-clic dimer acids produced from A -Octadecadienoic acid (linoleic acid).
The method of this invention is useful in protecting numerous copper alloys from corrosive attack by aerated aqueous solutions of commercial detergents containing effective amounts of polyphosphate builders. Copper alloys, having normally high corrosion resistance, which are readily attacked by aqueous, aerated, polyphosphate solutions include copper-zinc alloys containing 6090% by weight of copper, such as gilding metal, commercial bronze, red brass, spring brass, common brass, Muntz metals, and admiralty brass. Copper alloys containing minor amounts of metal such as zinc, lead, tin, aluminum, and nickel, such as forging brass, architectural bronze, aluminum brass, naval brass, nickel-aluminum bronze, aluminum bronze, and cupro-nickel, are also subject to corrosive attack and can be inhibited in accordance with this invention. The alloys protected can also contain minor amounts of manganese, beryllium or phosphorus.
It has been found that the alkali-metal polyphosphate salts responsible for accelerated corrosive attack upon normally corrosion-resistant copper alloys are the pyrophosphate, tripolyphosphate, hypophosphate, hexametaphosphate, and trimetaphosphate salts. Of these, the pyrophosphate, tripolyphosphate, and hexametaphosphate salts of sodium are especially likely to be found in commercial detergents, and result in serious corrosion problems when such detergents are employed in apparatus fabricated of copper alloys.
The effectiveness of the method of this invention for inhibiting corrosion, as well as the ineffectiveness of a wide variety of chemically similar corrosion inhibitors of the prior art, for inhibiting the corrosion of copper alloys contacted by aerated, aqueous solutions of commercial detergents has been demonstrated experimentally. First, a water solution of a commercial detergent composition containing mixed aryl alkyl sulfonates, sodium tripolyphosphate, sodium sulfate, and other com- .ponents (0.5 gram detergent per 100 millimeters of water) was prepared and divided into a plurality of Suflicient amounts of various inhibitors were added to each flask to produce an inhibitor concentration of 0.1 gram per 100 milliliters of solution. Finally, two brass strips /z inch by 3 inches) were immersed in the solutions in each flask, and air was bubbled through the solutions at a rate of 20-30 milliliters per minute for a period of 72 hours while the temperature was maintained at about 70 centigrade. Percent weight loss from the brass strips for each test are given in the following table.
TABLE I Inhibitor: Percent weight loss Blank 1.70 Dimer acid 0.25 Phthalic anhydride 0.90 Tall oil fatty acid 0.68 Linoleic acid 0.73 Triethylene tetramine 1.59 Linseed oil fatty acid 0.73 Rosin acid 1.32 Pine oil 1.78 Lithium ricinoleate 0.95
*Commercial dimer acids, about 85% dimerized linoleic acid, 15% acid monomers and trimers.
A further series of experiments was performed to establish that the effective agents causing the corrosion of normally corrosion-resistant copper alloys were polyphosphate builders usually employed in commercial detergents. These further experiments also establish that the dimer acids when employed in the method of this invention are effective for inhibiting corrosion induced by the presence of polyphosphates in aerated aqueous solutions. The results of the experiments are set forth in Table II.
TABLE II Comp., Deter., Inhib., Percent; Detergent Components Wt. Wt. Inhibitor Wt. Wt.
Percent Percent Percent Loss 100 0. 5 0. 25 $3 0. 5 -0. 11 40 Sodium sulfate 20 0. 5 0. 07 Trisodium ph0sphate 40 DB SS 40 Sodium sulfate 20 0. 5 1. 04 Sodium pyrophosphate 40 DBSS 40 Sodium sulfate 20 0. 5 Dimer 0.2 0.35 Sodium pyrophosphate 40 acid. DB SS 40 Sodium sulfate 20 0. 5 1. 33 Sodium tripolyphosphate" 40 DBSS 40 Sodium sulfate 20 0. 5 Dimer 0. 2 0. 28 Sodium tripolyphosphatc 40 acid Sodium pyrophosphate 100 O. 5 1. 75 Sodium pyrophosphate 100 0.5 Dungr 0.2 0 48 am Sodium tripolyphosphate 100 0. 5 1. 64 Sodium tripolyphosphate 100 0. 5 Din'ftt 0. 2 0. 20
1 Dodecylbenzene sodium sulfonate. 2 Commercial dimer acids, about dimerized linoleic acid and 15% monomers and trirners.
It will be noted that the dimer acids were not as effective in inhibiting corrosive attack upon copper alloys induced by the synthetic detergent compositions of Table II. This is believed to be because of the abnormally high concentration of polyphosphates in the compositions of Table II. In these experiments, the same procedures as described with reference to Table I were employed.
While the invention has been described with reference to commercial detergent solutions based upon alkaryl sodium sulfonates including polyphosphate builders, the method of this invention is useful in inhibiting corrosion produced by any detergent composition which includes polyphosphate builders.
This invention also contemplates and includes detergent compositions per se which employ polyphosphate builders and which include a small but effective amount of dimer acids to inhibit corrosion of copper alloys which would otherwise occur when the detergent is placed in aqueous solution and contacts structures fabricated of copper alloys. Thus, the detergent compositions of this invention will include any of a wide variety of cationic, nonionic, or anionic detergents which include a minor but effective amount of polyphosphate builders, and a small amount of dimer acid inhibitor. Especially preferred compositions are detergents based upon alkaryl sodium sulfonates, and including minor amounts, usually in the range of about 5-20%, of polyphosphate builders such as the alkali-metal pyrophosphate, tripolyphosphate, hexametaphosphate, trimetaphosphate, and hypophosphate salts. More preferably, the builders will be the solium salts such as sodium pyrophosphate, sodium tripolyphosphate, and sodium hexametaphosphate. A preferred detergent base is dodecylbenzene sodium sulfonate. The detergent composition will contain about 120% by weight, and preferably about 5% by weight, based upon the total weight of the detergent composition, of the aforedefined dimer acid.
A specific example of a detergent composition in accordance with this invention is as follows:
Dimer acids The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A composition consisting essentially of an alkaryl sodium sulfonate detergent, alkali-metal polyphosphate salts selected from the group consisting of sodium pyrophosphate, sodium tripolyphosphate, and sodium hexametaphosphate in an amount sufficient to inhibit metathesis aud about 120% by weight of the total composition of cyclic, dimerized acids having at least two olefinic linkages per molecule and being derivable from polyolefinic, monocarboxylic fatty acid monomers having at least carbon atoms per molecule.
2. A composition in accordance with claim 1 in which said detergent includes a major proportion of alkaryl sodium sulfonates.
3. A composition in accordance with claim 2 in which said sulfonate is dodecylbenzene sodium sulfonate.
4. The composition in accordance with claim 3 in which said dimeric acid is a dimer of A -octadecadienoic acid.
5. In the method of inhibiting the corrosion of coopercontaining metals in contact with aqueous, aerated solutions containing alkali-metal polyphosphate salts selected from the group consisting of sodium pyrophosphate, sodium tripolyphosphate, and sodium hexametaphosphate in amounts suflicient to promote corrosion of said copper- 6 containing metals the improvement consisting essentially of adding to the solutions about 0.005 to 0.1%, by Weight of said solution, of cyclic dimerized acids having at least two olefinic linkages per molecule and being derivable from polyolefinic monocarboxylic fatty acid monomers having at least 10 carbon atoms per molecule.
6. The method in accordance with claim 5 in which said solution is a detergent solution containing alkaryl sodium sulfonates.
7. The method in accordance with claim 6 in which said sulfonate is dodecylbenzene sodium sulfonate.
8. The method in accordance with claim 7 in which said dimerized acid is a dimer of A -octadecadienoic acid.
References Cited by the Examiner UNITED STATES PATENTS 2,618,604 11/1952 Schaefier et al. 252389 XR 2,763,612 9/1956 Raifsnider et al. 252-389 XR 2,773,032 12/1956 Cantrell et al. 252389 XR 2,861,954 11/1958 Ruff 252138 XR 2,954,347 9/1960 John et al. 252-138 XR LEON D. ROSDOL, Primary Examiner.
JULIUS GREENWALD, Examiner.
J. T. FEDIGAN, Assistant Examiner.
Claims (1)
1. A COMPOSITION CONSISTING ESSENTIALLY OF AN ALKARYL SODIUM SULFONATE DETERGENT, ALKALI-METAL POLYPHOSPHATE SALTS SELECTED FROM THE GROUP CONSISTING OF SODIUM PYROPHOSPHATE, SODIUM TRIPOLYPHOSPHATE, AND SODIUM HEXAMETAPHOSPHATE IN AN AMOUNT SUFFICIENT TO INHIBIT METATHESIS AND ABOUT 1-20% BY WEIGHT OF THE TOTAL COMPOSITION OF CYCLIC, DIMERIZED ACIDS HAVING AT LEAST TWO OLEFINIC LINKAGES PER MOLECULE AND BEING DERIVABLE FROM POLYOLEFINIC, MONOCARBOXYLIC FATTY ACID MONOMERS HAVING AT LEAST 10 CARBON ATOMS PER MOLECULE.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US209770A US3267038A (en) | 1962-07-13 | 1962-07-13 | Inhibiting the corrosion of coppercontaining metals |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US209770A US3267038A (en) | 1962-07-13 | 1962-07-13 | Inhibiting the corrosion of coppercontaining metals |
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| US3267038A true US3267038A (en) | 1966-08-16 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3538009A (en) * | 1967-02-01 | 1970-11-03 | Cincinnati Milling Machine Co | Method for reducing skin irritation in detergent compositions |
| DE3002175A1 (en) * | 1979-01-23 | 1980-07-31 | Toyo Aluminium Kk | METAL FLAKE PIGMENT PREPARATION AND METHOD FOR THE PRODUCTION THEREOF |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2618604A (en) * | 1949-11-25 | 1952-11-18 | Procter & Gamble | Polyphosphate-containing detergent compositions having decreased corrosivity toward aluminum |
| US2763612A (en) * | 1953-05-18 | 1956-09-18 | Shell Dev | Natural hydrocarbon production method |
| US2773032A (en) * | 1954-05-13 | 1956-12-04 | Gulf Oil Corp | Rust inhibiting lubricating oil compositions |
| US2861954A (en) * | 1956-01-09 | 1958-11-25 | Lever Brothers Ltd | Polyphosphate compositions containing soap and 2-mercaptothiazoline |
| US2954347A (en) * | 1955-10-27 | 1960-09-27 | Procter & Gamble | Detergent composition |
-
1962
- 1962-07-13 US US209770A patent/US3267038A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2618604A (en) * | 1949-11-25 | 1952-11-18 | Procter & Gamble | Polyphosphate-containing detergent compositions having decreased corrosivity toward aluminum |
| US2763612A (en) * | 1953-05-18 | 1956-09-18 | Shell Dev | Natural hydrocarbon production method |
| US2773032A (en) * | 1954-05-13 | 1956-12-04 | Gulf Oil Corp | Rust inhibiting lubricating oil compositions |
| US2954347A (en) * | 1955-10-27 | 1960-09-27 | Procter & Gamble | Detergent composition |
| US2861954A (en) * | 1956-01-09 | 1958-11-25 | Lever Brothers Ltd | Polyphosphate compositions containing soap and 2-mercaptothiazoline |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3538009A (en) * | 1967-02-01 | 1970-11-03 | Cincinnati Milling Machine Co | Method for reducing skin irritation in detergent compositions |
| DE3002175A1 (en) * | 1979-01-23 | 1980-07-31 | Toyo Aluminium Kk | METAL FLAKE PIGMENT PREPARATION AND METHOD FOR THE PRODUCTION THEREOF |
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