GB2294696A - Marine lubricant composition - Google Patents
Marine lubricant composition Download PDFInfo
- Publication number
- GB2294696A GB2294696A GB9521715A GB9521715A GB2294696A GB 2294696 A GB2294696 A GB 2294696A GB 9521715 A GB9521715 A GB 9521715A GB 9521715 A GB9521715 A GB 9521715A GB 2294696 A GB2294696 A GB 2294696A
- Authority
- GB
- United Kingdom
- Prior art keywords
- composition
- lubricant
- marine
- base oil
- aromatic amine
- 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.)
- Withdrawn
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- 239000000314 lubricant Substances 0.000 title claims abstract description 43
- 239000000203 mixture Substances 0.000 title claims abstract description 26
- 150000002148 esters Chemical class 0.000 claims abstract description 19
- 239000002199 base oil Substances 0.000 claims abstract description 16
- 230000007797 corrosion Effects 0.000 claims abstract description 12
- 238000005260 corrosion Methods 0.000 claims abstract description 12
- 150000004982 aromatic amines Chemical class 0.000 claims abstract description 10
- 239000003112 inhibitor Substances 0.000 claims abstract description 9
- 230000003301 hydrolyzing effect Effects 0.000 claims abstract description 8
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000003921 oil Substances 0.000 claims description 8
- 230000007062 hydrolysis Effects 0.000 claims description 4
- 238000006460 hydrolysis reaction Methods 0.000 claims description 4
- 230000001050 lubricating effect Effects 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 231100000111 LD50 Toxicity 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical class C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 claims description 2
- 230000000087 stabilizing effect Effects 0.000 claims description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims 2
- 239000010720 hydraulic oil Substances 0.000 claims 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
- 229940035422 diphenylamine Drugs 0.000 claims 1
- 125000004185 ester group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 abstract description 5
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 abstract description 4
- 235000010354 butylated hydroxytoluene Nutrition 0.000 abstract description 4
- 239000004322 Butylated hydroxytoluene Substances 0.000 abstract description 3
- LZJUZSYHFSVIGJ-UHFFFAOYSA-N ditridecyl hexanedioate Chemical compound CCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCC LZJUZSYHFSVIGJ-UHFFFAOYSA-N 0.000 abstract description 3
- 229940095259 butylated hydroxytoluene Drugs 0.000 abstract description 2
- 239000003381 stabilizer Substances 0.000 abstract description 2
- 239000006260 foam Substances 0.000 abstract 1
- -1 C12 monocarboxylic acids Chemical class 0.000 description 9
- 231100000584 environmental toxicity Toxicity 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 231100000636 lethal dose Toxicity 0.000 description 7
- 235000019198 oils Nutrition 0.000 description 7
- 238000009472 formulation Methods 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 5
- 235000006708 antioxidants Nutrition 0.000 description 5
- 150000002989 phenols Chemical class 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 241000143060 Americamysis bahia Species 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000002763 monocarboxylic acids Chemical class 0.000 description 3
- QAPVYZRWKDXNDK-UHFFFAOYSA-N P,P-Dioctyldiphenylamine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=C(CCCCCCCC)C=C1 QAPVYZRWKDXNDK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 229920013639 polyalphaolefin Polymers 0.000 description 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- MDWVSAYEQPLWMX-UHFFFAOYSA-N 4,4'-Methylenebis(2,6-di-tert-butylphenol) Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MDWVSAYEQPLWMX-UHFFFAOYSA-N 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- JRBRVDCKNXZZGH-UHFFFAOYSA-N alumane;copper Chemical compound [AlH3].[Cu] JRBRVDCKNXZZGH-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- HTMDHERCQUESGS-UHFFFAOYSA-N didecyl decanedioate Chemical compound CCCCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCCCC HTMDHERCQUESGS-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 231100000518 lethal Toxicity 0.000 description 1
- 230000001665 lethal effect Effects 0.000 description 1
- 239000003879 lubricant additive Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- FSWDLYNGJBGFJH-UHFFFAOYSA-N n,n'-di-2-butyl-1,4-phenylenediamine Chemical compound CCC(C)NC1=CC=C(NC(C)CC)C=C1 FSWDLYNGJBGFJH-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229940117969 neopentyl glycol Drugs 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 235000011044 succinic acid Nutrition 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000820 toxicity test Toxicity 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
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- 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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
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- 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
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/34—Esters of monocarboxylic acids
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- 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
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/36—Esters of polycarboxylic acids
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- 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
- C10M129/04—Hydroxy compounds
- C10M129/10—Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring
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- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/12—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to a carbon atom of a six-membered aromatic ring
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- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon only
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- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon only
- C10M133/46—Imidazoles
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- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/32—Heterocyclic sulfur, selenium or tellurium compounds
- C10M135/36—Heterocyclic sulfur, selenium or tellurium compounds the ring containing sulfur and carbon with nitrogen or oxygen
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- 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
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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- 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
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/024—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- 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
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/027—Neutral salts thereof
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- 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
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- 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
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- 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
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
- C10M2207/2815—Esters of (cyclo)aliphatic monocarboxylic acids used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
- C10M2207/2825—Esters of (cyclo)aliphatic oolycarboxylic acids used as base material
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Abstract
The composition contains a synthetic ester base oil and an aromatic amine and/or a hindered phonol as a hydrolytic stabilising agent. The lubricant is especially used in equipment operating in a marine environment e.g. sliding machine parts or hydraulic systems. A typical composition contains ditridecyl adipate (base oil), dioctyldiphenyl amine and butylated hydroxytoluene plus corrosion, rust and foam inhibitors.
Description
IMPROVED MARINE LUBRICANT WITH ENVIRONMENTAL AND
PERFORMANCE ADVANTAGES FTELD OF THE INVENTION
This invention relates to a more environmentally responsible marine lubricant useful for equipment operating in marine environments.
DESCRIPTION OF THE RELATED ART
Because of concerns over environmental issues, lubricants used in marine applications have come under increased scrutiny. Various non-mineral based vegetable and synthetic oils have been proposed as alternatives to conventional mineral base oils. Two environmental issues of concern to lubricants which may be released to the environment are ecotoxicity and biodegrability. S. J. Randles and M. Wright discuss these issues in a paper entitled "Environmentally Considerate Ester Lubricants for the Automotive and
Engineering Industries", Technische Akademie Esslinger 8th International "Tribology 2000" Colloquium, Proceedings VI (1992).
Rapeseed and other vegetable oils are generally more biodegradable than mineral oils. On the other hand, they suffer thermal and oxidative stability problems. Synthetic oils such as polyalphaolefins are stable but are not as biodegradable. Polyols and diesters are more biodegradable but tend to be susceptible to hydrolysis, particularly in hot aqueous environments.
It would be desirable to have a more environmentally responsible lubricant which is also hydrolytically stable for use in aqueous environments, especially lubricants which are exposed to aqueous environments at elevated temperatures.
SUMMARY OF THE INVENTION
The invention relates to a marine lubricant composition with improved stability in aqueous environments which comprises: (a) a synthetic ester base oil; (b) a hydrolytic stability agent, said agent containing from about 0.1 to about
3.0 wtO/o, based on lubricant composition, of at least one of an aromatic
amine and a hindered phenol.
In another embodiment, there is provided a method of lubricating machine parts in an aqueous marine environment which comprises lubricating the machine parts with the marine lubricant according to the invention. Yet another embodiment relates to a method for stabilizing a marine lubricant containing a synthetic ester base oil against hydrolysis which comprises incorporating into the base oil at least one of an aromatic amine and a hindered phenol.
DETAILED DESCRIPTION OF THE INVENTION
The term "marine lubricant" refers to lubricants used in a marine environment excluding lubricants for marine internal combustion engines, e.g., marine diesel engines and two-cycle engines. Lubricants for engines have different requirements from the present marine lubricants which are intended as lubricants for sliding machine parts and hydraulic systems which operate in an aqueous environment. Preferred marine lubricants are marine hydraulic fluids.
Synthetic ester base oils include esters of monocarboxylic and dicarboxylic acids, and esters prepared from C5 to C12 monocarboxylic acids and polyols. Suitable polyols include neopentylglycol, trimethylolpropane and pentaerythritol.
Preferred synthetic ester base oils are esters of monocarboxylic acids and dicarboxylic acids, especially esters of dicarboxylic acids Esters of monocarboxylic acids have the formula R1COOR where R is C1 to C10 alkyl and R1 is C8 to C20 alkyl or alkenyl. Esters of dicauboxylic acids have the formula
where R3 and R4 are each independently C6 to C20 alkyl, R5 is C1 to C4 alkyl or hydrogen and n is an integer from 1 to 10. Examples of preferred esters include ditridecyladipate, di-n-decylsebacate, di-2-ethylhexyladipate, di-2ethylhexyl-2,4-dimethyladipate, di-2-octylazelate and di-3,5,5-trimethylhexylsebacate.
Hydrolytic stability agents are at least one of an aromatic amine and a hindered phenol preferably hindered phenols. Preferred aromatic amines are those conventionally known in the art as antioxidants and include alkyl substituted diphenyl amines and phenyl naphthyl amines such as 4,4'-dioctyldiphenylamine, 4,4'-dodecyldiphenylamine, phenyl-alpha-naphthylamine, N,N' di-sec-butyl-p-phenylenediamine and the like.Preferred hindered phenols are those conventionally known in the alt as antioxidants and include sterically hindered monohydric and dihydric phenols such as 2,6-di-tert-butylphenol, 2,6di-tert-butyl-4-methylphenol, 4,4'-methylene bis(2,6-di -tert-butylphenol), and n octadecyl-3 ,5-di-tert-butyl-4-hydroxyhydrocinnamate. The preferred amounts of aromatic amine and/or hindered phenol is from 0.5 to 2.0 wtO/o, based on lubricant composition. The hydrolytic stability agents provide hydrolytic stability to the ester base oil especially under conditions favorable to hydrolysis such as high temperature and acidic!basic conditions.
The marine lubricant formulation preferably includes conventional corrosion inhibitors and iust inhibitors. Examples of corrosion inhibitors include thiazoles, triazoles, thiadiazoles, imidazolines, fatty acid amines, acid phosphates and their amine salts, amines and their salts, ethoxylated amines, phenols, and alcohols, dimer and trimer carboxylic acids, and the like. Examples of rust inhibitors include alkenyl succinic acids and anhydrides and their amino derivatives, sulfurized alkyl phenols, polyoxyalkylene polyols and the like. Corrosion and rust inhibitors are typically present in amounts of from 0.1 to 0.5 wtO/o, based on marine lubricant formulation.
If desired, the subject marine lubricant folmulation may contain other conventional additives such as antifoam agents, antiwear agents, antioxidants, extreme pressure agents, friction modifiers, other hydrolytic stabilizers and the like. The additives are disclosed, e.g., in "Lubricants and Related
Products", by Dieter Klamann, Verlag Chemie, Deerfield Beach, Florida, 1984.
Two factors which should be considered when there is likelihood of lubricant entering the marine environment are biodegradability and ecotoxicity. It is known that synthetic esters according to the invention are more biodegradable than other types of synthetic oils such as polyalphaolefins and more biodegradable than mineral oils. However, additive packages can affect both biodegrability and ecotoxicity. The present marine lubricants do not contain metals or dispersants which can adversely affect biodegrability and ecotoxicity. Also, ecotoxicity data is now required by some countries for materials which may be released to the aquatic environment. An accepted standard for ecotoxicity is the acute mysid toxicity test in which the LC50 lethal concentration required to kill 50% of the mysid shrimp population after 96 hours is measured.A LC50 value of 100 ppm is generally accepted as a standard for ecotoxicity. The greater the LC50 value, the less toxic the material. It is preferred that the marine lubricant formulations of this invention have LC50 values of 100 or greater.
While it is known that certain classes of chemicals commonly used as lubricant additives are undesirable based on their impact on biodegradability and/or ecotoxicity, such effects are typically concentration dependent. Thus it is difficult to predict the effect of any given additive package on ecotoxicity, and it is desirable to test such additive packages against an accepted standard such as the LC50 test.
The marine lubricant compositions of this invention can be used in equipment which are in service in aquatic environments, e.g., steam catapults on aircraft carriers, loading cranes, or hydraulic application where lubricant may be discharged to the environment.
This invention will be further understood by reference to the following examples which include a preferred embodiment of the invention.
Example 1
A marine lubricant formulation was prepared blending the components shown in Table 1.
TABLE 1
Amount, %
Component Function By Weight
1. ditridecyl adipate(a) base oil 97.75
2. dioctyldiphenyl amine(b) anti-oxidant 1.00
3. butylated hydroxytoluene(c) anti-oxidant 1.00
4. alkylated benzotriazole(d) corrosion inhibitor 0. 10
5. succinic anhydride amine(e) anti-rust 0.10
6. silicone polymer(f) anti-foam 0.05 (a) Vistone A30 available from Exxon Chemical Company.
(b) Vanlube 81 available from R. T. Vanderbilt Company.
(c) Navgard BHT available from Uniroyal Chemical Company.
(d) Reomet 39 available from Ciba-Geigy Company.
(e) Mobilad C-603 available from Mobil Chemical Company.
(f) PC-I 244 available from Monsanto Company.
This lubricant formulation is clear, leaves no sheen on water and has a low pour point of less than -50 C. Pour points of-24"C or lower are desirable for operations in cold environments.
LC50 values were evaluated using mysid shrimp, mysidopsis bahia. Nominal loading concentrations of lubricant for the test were 500 mg/l, 250 mg/l, 125 mg/l, 62.5 ml/l, 31.2 mdl with a natural sea water control. These samples were mixed in a mixing vessel for 24 hours followed by a one hour settling period.
The Water Accommodated Fraction (WAF) was drawn through the outlet at the bottom of the mixing vessel and distributed into two replicate chambers with a separate aliquot prepared for water quality measurements.
Water quality measurements (dissolved oxygen, pH, salinity and temperature) were performed on each treatment on Day 0 and at termination. Mysids were exposed for a 96-hour period.
The Lethal Concentration (LC50) value is the calculated nominal loading concentration that is lethal to 50% of a population of test organisms during a specified period. The 96-hour LCS0 value was 182.5 mg/l with 95% confidence intervals of 150.4 to 230.3 mg/l.
This value of 182.5 mg/l (182.5 ppm) compared to an accepted standard of 100 ppm demonstrates that the marine lubricant formulation has a low level of toxicity.
Example 2
This example demonstrates the capability of the oil of Example 1 to provide metal protection in a hot aqueous environment relative to the base oil alone or a commercial navy catapult oil using a bench test described as follows.
The bench test involves aluminum and copper composition beakers filled with 90% lubricant and 10% water stored at 1800F for 60 days. Following completion of the bench test, the metal coupons were died and evaluated visually for evidence of corrosion. The results are summarized in Table 2.
TABLE 2
SAMPLE COPPER ALUMINUM l(a) slight tarnish, light orange shiny metal appearance
color similar to freshly similar to fresh aluminum
polished sample sample
2(b) dark tarnish, transparent moderate tarnish, metal
blank streaked with dark lines 3(c) graphite black tarnish, metal discolored (a) Lubricant of Example 1.
(b) Commercial oil used for Navy catapult systems.
(c) Base oil of Example 1.
These results demonstrate that in a hot aqueous environment, the lubricant oil according to the invention is stable and offers good metal protection relative to Samples 2 or 3, which showed substantial corrosion. A comparison of
Samples 1 and 3 shows that base oil alone without additives according to the invention undergoes significant corrosion under test conditions. Tests on other synthetic esters with and without the presence of water (no additives) indicates that ester hydroysis is a significant factor in metal corrosion. The metal sample with water present showed substantial corrosion whereas the sample without water showed no corrosion (no tamish) under test condition noted above.
Claims (12)
1. A marine lubricant composition with improved stability in aqueous environments which comprises: (a) a synthetic ester base oil; (b) a hydrolytic stability agent, said agent containing from about 0.1 to about
3.0 Wt0/o, based on lubricant composition, of at least one of an aromatic
amine and a hindered phenol.
2. The composition of claim I wherein the marine lubricant is a marine hydraulic oil.
3. The composition of claim 1 wherein the hydrolytic stability agent is a combination of aromatic amine and hindered phenol.
4. The composition of claim 1 wherein the aromatic amine is alkyl substituted diphenyl amine or phenyl naphthyl amine.
5. The composition of claim 1 wherein the hindered phenol is a sterically hindered monohydric or dihydric phenol.
6. The composition of claim 1 additionally comprising a corrosion inhibitor.
7. The composition of claim 1 additionally comprising a rust inhibitor.
8. The composition of claim 1 wherein the synthetic ester is an ester of a dicarboxylic acid.
9. The composition of claim 2 wherein the marine hydraulic oil is a catapult oil.
10. The composition of claim 1 wherein the LC50 value is at least 100 ppm.
11. A method for lubricating sliding machine parts in an aqueous environment which comprises lubricating the machine parts with the lubricant
composition of claim 1.
12. A method for stabilizing a maine lubricant containing a
synthetic ester base oil against hydrolysis which comprises adding to the base oil
from about 0.1 to about 3.0 wt%, based on lubricant, of at least one of an
aromatic amine and a hindered phenol.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US33470394A | 1994-11-04 | 1994-11-04 |
Publications (2)
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GB9521715D0 GB9521715D0 (en) | 1996-01-03 |
GB2294696A true GB2294696A (en) | 1996-05-08 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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GB9521715A Withdrawn GB2294696A (en) | 1994-11-04 | 1995-10-24 | Marine lubricant composition |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2019110355A1 (en) * | 2017-12-04 | 2019-06-13 | Basf Se | Branched adipic acid based esters as novel base stocks and lubricants |
Citations (9)
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GB1215433A (en) * | 1968-03-25 | 1970-12-09 | Stauffer Chemical Co | High temperature antioxidants and lubricants containing same |
GB1236740A (en) * | 1969-04-11 | 1971-06-23 | Geigy Uk Ltd | Tertiary alkylated diphenylamines and their uses as antioxidants |
GB1296087A (en) * | 1969-09-22 | 1972-11-15 | ||
GB1393366A (en) * | 1971-10-06 | 1975-05-07 | Exxon Research Engineering Co | Antioxidants |
EP0232154A2 (en) * | 1986-02-04 | 1987-08-12 | Nippon Oil Co. Ltd. | Lubricating oil compositions |
EP0387979A1 (en) * | 1989-01-13 | 1990-09-19 | Nippon Oil Company, Limited | Use of a p,p'-Dinonyldiphenylamine in a composition having a reduced tendency to form sludge in oil |
EP0417036A2 (en) * | 1989-08-30 | 1991-03-13 | Ciba-Geigy Ag | Butenyl aromatic amine stabilizers |
WO1991013133A2 (en) * | 1990-02-23 | 1991-09-05 | The Lubrizol Corporation | High temperature functional fluids |
EP0538195A2 (en) * | 1991-10-18 | 1993-04-21 | Ciba-Geigy Ag | N-Allyl/benzyl substituted phenylenediamine stabilizers |
-
1995
- 1995-10-24 GB GB9521715A patent/GB2294696A/en not_active Withdrawn
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1215433A (en) * | 1968-03-25 | 1970-12-09 | Stauffer Chemical Co | High temperature antioxidants and lubricants containing same |
GB1236740A (en) * | 1969-04-11 | 1971-06-23 | Geigy Uk Ltd | Tertiary alkylated diphenylamines and their uses as antioxidants |
GB1296087A (en) * | 1969-09-22 | 1972-11-15 | ||
GB1393366A (en) * | 1971-10-06 | 1975-05-07 | Exxon Research Engineering Co | Antioxidants |
EP0232154A2 (en) * | 1986-02-04 | 1987-08-12 | Nippon Oil Co. Ltd. | Lubricating oil compositions |
EP0387979A1 (en) * | 1989-01-13 | 1990-09-19 | Nippon Oil Company, Limited | Use of a p,p'-Dinonyldiphenylamine in a composition having a reduced tendency to form sludge in oil |
EP0417036A2 (en) * | 1989-08-30 | 1991-03-13 | Ciba-Geigy Ag | Butenyl aromatic amine stabilizers |
WO1991013133A2 (en) * | 1990-02-23 | 1991-09-05 | The Lubrizol Corporation | High temperature functional fluids |
EP0538195A2 (en) * | 1991-10-18 | 1993-04-21 | Ciba-Geigy Ag | N-Allyl/benzyl substituted phenylenediamine stabilizers |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019110355A1 (en) * | 2017-12-04 | 2019-06-13 | Basf Se | Branched adipic acid based esters as novel base stocks and lubricants |
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