CA2032940C - Metal free lubricants - Google Patents
Metal free lubricants Download PDFInfo
- Publication number
- CA2032940C CA2032940C CA002032940A CA2032940A CA2032940C CA 2032940 C CA2032940 C CA 2032940C CA 002032940 A CA002032940 A CA 002032940A CA 2032940 A CA2032940 A CA 2032940A CA 2032940 C CA2032940 C CA 2032940C
- Authority
- CA
- Canada
- Prior art keywords
- carbon atoms
- lubricant composition
- composition according
- hydrogen
- wear
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000314 lubricant Substances 0.000 title claims abstract description 47
- 229910052751 metal Inorganic materials 0.000 title claims description 6
- 239000002184 metal Substances 0.000 title claims description 6
- 239000000203 mixture Substances 0.000 claims abstract description 82
- -1 amino succinate ester Chemical class 0.000 claims abstract description 55
- 239000000654 additive Substances 0.000 claims abstract description 43
- 230000000996 additive effect Effects 0.000 claims abstract description 33
- 238000005260 corrosion Methods 0.000 claims abstract description 25
- 230000007797 corrosion Effects 0.000 claims abstract description 22
- 239000003112 inhibitor Substances 0.000 claims abstract description 17
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000005864 Sulphur Substances 0.000 claims abstract description 11
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 7
- 239000011574 phosphorus Substances 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 39
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 25
- 239000001257 hydrogen Substances 0.000 claims description 25
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
- 239000012141 concentrate Substances 0.000 claims description 12
- 229910019142 PO4 Inorganic materials 0.000 claims description 9
- 235000003704 aspartic acid Nutrition 0.000 claims description 9
- CKLJMWTZIZZHCS-REOHCLBHSA-N aspartic acid group Chemical group N[C@@H](CC(=O)O)C(=O)O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims description 9
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 claims description 9
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 claims description 8
- 239000003921 oil Substances 0.000 claims description 8
- 235000019198 oils Nutrition 0.000 claims description 8
- 239000010452 phosphate Substances 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 7
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 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 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
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
- 239000011707 mineral Substances 0.000 claims description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 4
- 239000008158 vegetable oil Substances 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 3
- 150000002431 hydrogen Chemical group 0.000 claims description 3
- YDOLGQNXROBHNZ-UHFFFAOYSA-N hydroxy-diphenoxy-sulfanylidene-$l^{5}-phosphane Chemical group C=1C=CC=CC=1OP(=S)(O)OC1=CC=CC=C1 YDOLGQNXROBHNZ-UHFFFAOYSA-N 0.000 claims description 3
- 229920001021 polysulfide Polymers 0.000 claims description 3
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims description 3
- BAOKQSCVBRNVKX-UHFFFAOYSA-N [2,3-di(nonyl)phenoxy]-dihydroxy-sulfanylidene-lambda5-phosphane Chemical compound CCCCCCCCCC1=CC=CC(OP(O)(O)=S)=C1CCCCCCCCC BAOKQSCVBRNVKX-UHFFFAOYSA-N 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- CCLBBCBPHBBKKD-UHFFFAOYSA-N dibutoxy-hydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCOP(O)(=S)OCCCC CCLBBCBPHBBKKD-UHFFFAOYSA-N 0.000 claims description 2
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims description 2
- JOVBTVIBOUJCPQ-UHFFFAOYSA-N hydroxy-bis(2-methylpropoxy)-sulfanylidene-$l^{5}-phosphane Chemical compound CC(C)COP(O)(=S)OCC(C)C JOVBTVIBOUJCPQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000010687 lubricating oil Substances 0.000 claims description 2
- 239000003208 petroleum Substances 0.000 claims description 2
- 229920013639 polyalphaolefin Polymers 0.000 claims description 2
- 239000005077 polysulfide Substances 0.000 claims 2
- 150000008117 polysulfides Polymers 0.000 claims 2
- 239000012530 fluid Substances 0.000 abstract description 24
- 229910001385 heavy metal Inorganic materials 0.000 abstract description 4
- 230000007613 environmental effect Effects 0.000 abstract description 2
- 238000012360 testing method Methods 0.000 description 17
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 6
- 239000002199 base oil Substances 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 229920000768 polyamine Polymers 0.000 description 4
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- 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 2
- QDCPNGVVOWVKJG-VAWYXSNFSA-N 2-[(e)-dodec-1-enyl]butanedioic acid Chemical compound CCCCCCCCCC\C=C\C(C(O)=O)CC(O)=O QDCPNGVVOWVKJG-VAWYXSNFSA-N 0.000 description 2
- AAIUWVOMXTVLRG-UHFFFAOYSA-N 8,8-dimethylnonan-1-amine Chemical compound CC(C)(C)CCCCCCCN AAIUWVOMXTVLRG-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000007866 anti-wear additive Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 150000002194 fatty esters Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229940119170 jojoba wax Drugs 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- LQNPIBHEOATAEO-UHFFFAOYSA-N octanoate;octylazanium Chemical compound CCCCCCCCN.CCCCCCCC(O)=O LQNPIBHEOATAEO-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 229960002317 succinimide Drugs 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- 229960001124 trientine Drugs 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 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 1
- DMLQDPIAVJTTKJ-UHFFFAOYSA-N 2-nonyl-n-(2-nonylphenyl)aniline Chemical compound CCCCCCCCCC1=CC=CC=C1NC1=CC=CC=C1CCCCCCCCC DMLQDPIAVJTTKJ-UHFFFAOYSA-N 0.000 description 1
- WVRNUXJQQFPNMN-VAWYXSNFSA-N 3-[(e)-dodec-1-enyl]oxolane-2,5-dione Chemical compound CCCCCCCCCC\C=C\C1CC(=O)OC1=O WVRNUXJQQFPNMN-VAWYXSNFSA-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
- 235000019737 Animal fat Nutrition 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Natural products CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- ZDWGXBPVPXVXMQ-UHFFFAOYSA-N bis(2-ethylhexyl) nonanedioate Chemical compound CCCCC(CC)COC(=O)CCCCCCCC(=O)OCC(CC)CCCC ZDWGXBPVPXVXMQ-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- BVEGNPSFKQMTQZ-UHFFFAOYSA-N calcium;1,2-di(nonyl)naphthalene Chemical compound [Ca].C1=CC=CC2=C(CCCCCCCCC)C(CCCCCCCCC)=CC=C21 BVEGNPSFKQMTQZ-UHFFFAOYSA-N 0.000 description 1
- MKFUUBCXQNCPIP-UHFFFAOYSA-L calcium;2,3-di(nonyl)naphthalene-1-sulfonate Chemical compound [Ca+2].C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1.C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1 MKFUUBCXQNCPIP-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- WIYAGHSNPUBKDT-UHFFFAOYSA-N dinonyl hexanedioate Chemical compound CCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCC WIYAGHSNPUBKDT-UHFFFAOYSA-N 0.000 description 1
- XWVQUJDBOICHGH-UHFFFAOYSA-N dioctyl nonanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCC(=O)OCCCCCCCC XWVQUJDBOICHGH-UHFFFAOYSA-N 0.000 description 1
- LAWOZCWGWDVVSG-UHFFFAOYSA-N dioctylamine Chemical compound CCCCCCCCNCCCCCCCC LAWOZCWGWDVVSG-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- ICTVPOAERFKXSS-UHFFFAOYSA-N ethyl 2-[3,5-bis(trifluoromethyl)phenyl]acetate Chemical class CCOC(=O)CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 ICTVPOAERFKXSS-UHFFFAOYSA-N 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- CVVVRVRQWUMYNX-UHFFFAOYSA-N n,n-bis(prop-2-enyl)formamide Chemical compound C=CCN(C=O)CC=C CVVVRVRQWUMYNX-UHFFFAOYSA-N 0.000 description 1
- XTAZYLNFDRKIHJ-UHFFFAOYSA-N n,n-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000008301 phosphite esters Chemical class 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229920001603 poly (alkyl acrylates) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229960005137 succinic acid Drugs 0.000 description 1
- 235000011044 succinic acid Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
-
- 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
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/10—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
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- C—CHEMISTRY; METALLURGY
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Lubricant compositions especially useful as hydraulic fluids contain a metal-free anti-wear or load-carrying additive containing sulphur and/or phosphorus and an amino succinate ester as corrosion inhibitor. Such compositions are free from heavy metal and have improved environmental acceptability where heavy metals are to be avoided, e.g. in agriculture. The lubricant base stock may be a biodegradable natural oil.
Description
Patents JFS :lan r METAL FREE LUBRICANTS
This invention relates to lubricant compositions, and more especially to lubricant compositions which can be used as hydraulic fluids.
Lubricant compositions normally contain a variety of additives incorporated to improve the performance of the lubricant in the environment in which it is to be used.
Such additives often contain transition metals. As is well known, there is now a general need, for environmental reasons, to reduce the use of transition metals which are frequently toxic. For example, lubricants used as hydraulic fluids often contain, as an anti-wear additive, a zinc dialkyl dithiophosphate (a so-called "ZDDP"). It is desirable to be able to provide hydraulic fluids which are zinc free: This is especially true where the hydraulic fluid is to be used in agriculture or arbariculture where spillage of the fluid onto cultivated land may occur and cause pollution of the land and of any drainage or river system connected with it.
It is also desirable on practical grounds to be able to provide an additive system which is suitable for use in all types of hydraulic fluid irrespective of the particular equipment in which it will be used. A universal anti-wear (UAW) additive system for,. use in such hydraulic fluids must be capable of providing fluids capable of meeting the specifications of the leading hydraulic pump manufacturers, e.g. the Haglunds-benison HFO specification and the Vickers Vane pump specification. It is a further requirement for such fluids that they must meet higher than load stage 10 performance in the FZG test described in more detail below.
Hydraulic fluids incorporating ZDDPs do not always give the required performance in the FZG test.
There is therefore a need for a metal-free universal anti-wear additive system suitable for use in lubricant compositions to be used in, for example, piston and screw compressors, industrial gear systems, and, more particularly, in hydraulic fluids.
According to the present invention, a lubricant composition comprises (a) a metal~free anti°wear or load carrying additive containingsulphur and/or phosphorus, and (b) a corrosion inhibitor in the form of an amino succinate ester of formula ... ,.,.. R3R4C_COORl .
R6R~~-,CRS-CCt~R2 _ in which Rl and R2 are each alkyl of 1 to 30, preferably 1 to 12, carbon atoms, R3, R4 and R5 are each hydrogen or alkyl of 1 to 4 carbon atoms, and R6 and R~ are each.
hydrogen" alkyl or l to 30 carbon, atoms, or an aryl group derived from a saturated or u~sa~urated carboxylic acid of up to 30 carbon atoms, at least one of R6 and R~ being a said acyl group. Preferably Rl.and R2 are each alkyl of 3 to 6 carbon atoms,..e,g, isobutyl, R3, R4 and RS are each hydrogen,, and Rg and:R~ axe each alkyl of 15 to 20 carbon atoms or an acyl radical derived from a saturated or ' -3-unsaturated dicarboxylic acid containing 4 to 10 carbon atoms, e.g, octadecyl, octadecenyl, or 3-carboxy-1-oxo-2-propenyl. An especially preferred component (b) is aspartic acid, N-(3-carboxy-1-axa-2-propenyl)-N-octadecyl-bis (2-methylgropyl)ester.
The metal free, and preferably ashless, anti-wear or load carrying additive may be any one of a wide range of sulphur- and/or phosphorus-containing additives, for example a mono- and/or di-hydrocarbyl phosphate or phosphite wherein the hydrocarbyl radical is alkyl of up to l2 carbon atoms, e.g. n-butyl, iso-butyl, n-amyl, n-octyl, 2-ethylhexyl or n-dodecyl, or a mixture thereof, and amine salts of such phosphates and phosphites, for example with primary amines of 4 to 18 carbon atoms, e.g» n-butylamine, n-octylamine, tert-octyZ primary amine, n-dodecylamine, the commercially available mixture of tertiary alkyl primary amines such as Primene 81R in which the tertiary alkyl radicals contain. l2 to 14 carbon atoms each, n-octadecylamine, aleylamine, and also secondary and tertiary amines such as di-n-octylamine, and tri-n-octylamine.
Other metal-free anti-wear or load carrying additives which can be used in the compositions of the present invention are sulphurized hydrocarbyl phosphites such as mono-- and di-hydrocarbyl thiophosphates wherein the hydrocarbyl radical may be aryl, e.g, phenyl, alkylaryl, e.g. alkylphenyl in which the alkyl contains up to 12 carbon atoms, arylalkyl, or aliphatic, e.g, alkyl of up to 12 s carbon atoms. Examples of such sulphurized hydrocarbyl phosphites includes diphenylthiophosphate, dinonylphenyl thiophosphates, di-n-butyl thiophosphate, di-isobutyl thiophosphate and di-2-ethylhexyl thiophosphate. Amine salts of such thiophosphates may also be used.
The anti-wear or load-carrying additive may also be a tri-hydrocarbyl di-thiophosphate in which each hydrocarbyl group may be, for example, an aromatic, alkylaromatic, cycloaliphatic, or aliphatic radical as aforesaid, e.g.
isopropyl, n-butyl, isobutyl, n-pentyl, n=hexyl, 2-ethylhexyl or n-dodecyl. The hydrocarbyl group may also be an alkenyl or cycloalkyl radical.
Other metal free antiwear or load carrying additives which can be used in the invention are sulphurized alkenes, e.g. sulphuri,zed isobutene, containing, for example 42 to 48~.by weight of sulphur or a sulphurized carboxylic acid or ester thereof in which the acid is,,for,example a fatty acid such as oleic or linoleic acid, e.g, a sulphurized vegetable oil or animal fat such as rape seed oil or lard oil.
Suitable cammercially available sulphurised fatty ester materials of, this type. include Sulperm lOS (Keil Chemical) and EP Oil GE10 ~Hornett). These typically contain about 9.5o and about 8.5-9.5% sulphur, respectively.
Dialkylpolysulphides such as t-nonyl trisulphide or t-dodecyl pentasulphide can also be used as the anti-wear or load-carrying additive.
The sulphur or phosphorus containing anti-wear or load carrying additive is advantageously prepared in the way described in our British Patent Application No. 8829597.7.
These anti-wear or load-carrying additives are amine salts of phosphorothioic acids of formula:
_5_ (RO) 2PS0-.H~I~R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and Rl, R2 and R3 are each hydrogen or substituted or unsubstituted hydrocarbyl radicals of up to 22 carbon atoms, not more than 2 of R1, R2 and R3 being hydrogen. When produced by the pracess of the aforesaid application, such salts have a purity of at least 95~ and have little reactivity towards copper, and less than 3$ of a phosphate of formula (RO)2POH in which R is as hereinbefore defined or amine salt thereof. Preferred such amine salts are those in which R is alkyl of 3 to 8 carbon atoms or phenyl and each of R1, R2 and R3 is hydrogen or an alkyl, cycloalkyl or alkenyl radical of 4 to 22 carbon atoms, not more than 2 of Rl, R2 and R3 being hydrogen. Preferably R
is phenyl, R1 and ~2 are hydrogen, and R3 is mixed C12-C14 tertiary alkyl.
Such amine salts are made by forming a mixture of sulphur and the amine in the liquid state, adding to the mixture a phosphate ester of formula (RO)2POH in an amount at least equivalent to the amount of sulphur under conditions such that the sulphur reacts with the ester but the reaction temperature does not rise above 130oC, and then continuing the reaction untal the solid sulphur has substantially disappeared from the reaction mixture. The quantity of amine is adjusted if necessary so that the total quantity of amine is at least equivalent to the quantity of the phosphite ester.
Compatible mixtures of such anti-wear or load-carrying additives can, of course, :also be used.
The proportions of components (a) and (b) in the lubricant compositions of the invention are preferably from 0.05$ to 3$, preferably 0.1$ to 1.5$, of the antiwear or load carrying additive and from 0.002$ to 0.5~, preferably 0.05 to 0.25, by weight of the corrosion inhibitor, such percentages being by weight based on the total weight of the lubricant composition.
The lubricant composition may include as the base fluid any mineral or non-mineral oil suitable for use as a lubricant, or more especially as a hydraulic fluid. Such base stocks include paraffinic lubricating oil base stocks of mineral origin, synthetic oils such as polyalphaolefins, e.g. hydrogenated polydecene, synthetic lubricant. esters, such as dialkyl adipates and azelates (in which the alkyl groups typically have l to 20 carbon atoms each, e.g.
dioctyl azelate, dinonyl adipate, or di-2-ethylhexylazelate) and oils of biological origin including more particularly lubricant vegetable oils such as rape seed oil, jojoba oil, cotton seed oil, peanut oilyor palm oil.
It is a particular advantage of the invention that the combination of components (a) and (b) as set out above is compatible with a variety of oils of natural, especially vegetable, origin suitable for use as hydraulic fluids.
Such natural oils are biodegradable, and in conseguence,the . _7-present invention makes it possible to provide an effective hydraulic fluid based on a biodegradable base stock such as rape seed oil or jojoba oil and incorporating additives which are free from heavy metals.
When it is to be used in an acidic environment, it can be desirable to incorporate in a lubricant composition of the present invention a third component, vie. (c) an alkaline earth metal alkylbenzene sulphanate, alkyl-naphthalene sulphonate, petroleum sulphonate, alkylphenate, alkyl sulphurized phenate, or alkylsalicylate. This material is usually overbased and may also be sulphuri2ed.
A sulphurized overbased calcium alkylphenate in which the . alkyl group is paranonyl, or a calcium dinonylnaphthalene-sulphonate is preferably used. The proportion of such additional additive is usually in the range 0.005 to 0.50$
based on the total weight of the composition. Such compositions are not ashless, but they do not contain heavy metals and thus achieve one of the major objectives of the present invention.
The lubricant compositions of the present invention may incorporate other additives conventionally used in lubricants, for example:
(i) Additional corrosion inhibitors, e.g. amine salts of carboxylic acids such as octylamine octanoate, condensation products of dodecenyl succinic acid or anhydride and a fatty acid such as oleic acid with a polyamine, e.g. a polyalkylene polyamine such as -g_ triethylenetetramine, and half esters of alkenyl succinic acids in which the alkenyl radical contains 8 to 24 carbon atoms with alcohols such as polyglycols.
(ii) Ashless dispersants, especially those made by reaction of a polyolefin malefic anhydride reaction product with a polyalkylene polyamine such as triethylene tetramine or tetraethylene pentamine. In such dispersants, the polyolefin is typically polyisobutene having a number average molecular weight of 900 to 1200.
In some circumstances, it may be advantageous to boronate such ashless dispersants. While boron is non-metal, it is ash-forming and its use in the compositions of the invention is not preferred.
(iii) Antioxidants including, for example, phenolic antioxidants such as 2,6-di-tert-butylphenol, 2,6-di-tert-butyl-4-methylphenol, and 4,4°-methylenebis(2,6-di-tertbutyl-phenol), sulphurized phenolic antioxichnts such as 4,4'-thiobis(6-tent-butyl-o-cresol) and aromatic amines such as di(nonylphenyl)amine and octylated phenyl-alpha--naphthylamine., Mixtures of phenolic antioxidants and aromatic amine. antioxidants (e.g., ETHYL~ Antioxidant 728 and/or 733.wi~h Nauga;lube 438L) are preferred.
(iv) Copper deactivators, e.g. benzotriazole and its derivatives, thiadiazoles and their derivatives, ar tricr~esyl phosphate. , (v) Demulsifying agents, more particularly, surfactants which are preferably ashless, e.g. non-ionic surfactants such as polyglycols.
(vi) Viscosity index improvers, e.g.
' -9-poly(alkylmethacrylates) and olefin copolymers such as ethylene/propylene and styrene/isoprene copolymers, and dispersant viscosity index improvers such as copolymers, of an alkylmethacrylate with N-vinylpyrrolidone and olefin copolymers grafted with nitrogen-containing monomers such as diallylformamide.
(vii) Pour point depressants such as poly(alkyl-methacrylates).
(viii) Anti-foam agents,.e.g. products based on silicones and poly(alkylacrylates).
All such additional ingredients must of course be compatible with components (a) and (b) but, subject to this, they are used in the usual proportions.
The compositions of the invention are conveniently supplied to the formulator of the finished lubricant composition in the form of an additive concentrate comprising the components (A) and (B) as aforesaid, alone or preferably with a relatively small amount of suitable base oil to facilitate handling, and optionally with one or more of the additional ingredients mentioned above. In such concentrates the amounts of components (A) and (B) are proportioned such that when the concentrate is blended into a base fluid to provide a finished lubricant composition in which the concentration of component (A) is from 0.05 to 3% by weight and preferably from 0.1 to 1.5o by weight based on the total weight of the lubricant composition, the cancentration of component (B) is from 0.002 to 0.5o by weight and preferably from 0.05 to 0.25 % by weight based on the total weight of the lubricant composition. Thus the ratio of (A) to (B) in such concentrates is preferably 30:1 to 0.4:1. The proportion of component (B) in the concentrate is preferably from 0.1 to 50o by weight, especially 0.1 to 10%, and most commonly 1 to 5% by weight of the concentrate.
The following Examples illustrate the invention.
~iydraulic fluid blends were prepared using as the base stock an ISO 46 mineral base oil having a kinematic viscosity range at 40°C of from 41.4 to 50.6 cSt. The additives incorporated were as stated below. Each blend was evaluated for clarity and by the IP 1358 corrosion test.
The latter test involves stirring a mixture of 300 ml of the hydraulic fluid with 30 ml of artificial sea water at a temperature of 60°C with a steel cylinder immersed in the mixture. The test was run in duplicate for 24 hours with each blend and the immersed steel specimens were then examined for signs of rusting. For a pass, no rust must be visible on the specimen.
The blends were also examined by the FZG test (IP334/79). In this test two steel spur gears are rotated together with oil dip lubrication for a series of.l5 minute stages. The relative torque between the gears is increased by a,fixed amount after each stage and' the gears are run together. for a.given period after which they are examined for wear or damage: The result of the test is quoted in -l0A-terms of the final pass stage and the first fail stage. To be satisfactory, the pass stage must be higher than 10.
The following Tables I and II set out the compositions of the hydraulic fluids tested and the results obtained with each. Blend 4, 5, 6, 7 and 10 are in accordance with the present invention. The other blends are for comparison.
HYDRAULIC FLUID BASE OIL
Blend 1 2 3 4 5 6 Component AZ 0.07 0.07 0.07 0.07 0.07 0.1 Component A2 0.19 0.19 0.19 0.19 0.19 0.12 Component B - - - 0.02 0.02 0.015 Corrosion Inhib. D 0.065 - 0.04 0.03 0.025 0.025 Corrosion Inhib. E - 0.02 - - - -Corrosion Inhib. F - - 0.075 - - -FZG Load 12 Pass 9 Pass/Not 12 Pass 12 Pass12 Pass Stage Fail 10 FailTested IP 135 B Fail Fail Not Pass Pass Pass Test Result ModerateSevere Tested No rust No rustNo rust Rust Rust ' Clarity of Blended fluid Clear Clear Cloudy Clear Clear Clear Component AZ was the Primene 81R salt of diphenylthiophosphate.
Component A2 was a blend of 36$ di-t-nonyl polysulphide and 64$
sulphurised fatby ester Component B was aspartic acid, N-(3 carboxy-2-oxo-2-propenyl)-N-octadecyl-bis(2-methylpropyl)ester.
Corrosion Inhibitar D was a condensation product of dodecenyl succinic acid and oleic acid with a polyethylene polyamine Corrosion Inhibitor E was octylamine octanoate.
Corrosion Inhibitor F was a modified imidazoline (Monamulse CI) Blends 1-6 contained the same levels of conventional antioxidant, copper deactivator and demulse aid.
Blends 2 and 5 additionally contained a boronated polyisobutenyl succinimide ashless dispersant in conventional amount. In blend 6, component Al was prepared in the way described in British Patent Application 8829597,7 ~, l TABLE II
CONCENTRATIONS IN WT PERCENTAGE IN IS046 flYDRAULIC
FLUID BASE OIL
Blend 7 8 9 10 Component A1 0.07 0.07 0.07 0.07 Component A2 0.19 0,19 0.19 0.19 Component B 0.04 - -- 0,02 Detergent C 0.04 (C1) 0.04 (C1) 0.04 (C1) 0.0075 (C2) Corrosion Inhib.F - 0.04 - -Corrosion Inhib.G - - 0.03 -Corrosion Inhib.D 0.05 0.05 0.05 0.025 Clarity of Blended Fluid Clear Cloudy flazy Clear IP135B...Test Result Pass Pass Pass Pass FZG Load Stage Fail 11 Pass/ 11 Pass/ ll Pass/ 11 Pass/
-- 12 Fail 12 Fail 12 Fail 12 Fail Components A1, A2, B, D and F were as in Table I.
Detergent CZ was an overbased calcium sulphurised nonyl-phenate.
Detergent C2 was calcium dinonyl naphthalene sulphonate Corrosion Inhibitor G was butanedioic acid, sulpho-1,4-tridecyl ester, sodium salt.
Blends 7, 8 and 9 contained the same levels of conventional antioxidant, copper deactivator, VI improver and demulse aid.
Blend 10 similar to blends 7 to 9 but contained a boronated polybutenyl succinimide ashless dispersant in conventional amount and no VI improver.
In a furthe=r experiment, a blend 11 was made having the same composition as blend 6 except that the base oil was rape seed oil. The results in the FZG test, the IP135B
test, and the clarity of the blend were the same as those obtained with b7Lend 6.
In another experiment, a blend 12 was made having the same composition as blend 6 except that component A1 was used at a concentration of 0.11 weight percent, and component A2 was composed entirely of the sulphurised fatty ester (Sulperm lOS). Blend 12 produced the same FZG, IP135B, and clarity results as blend 6. In performance testing, blend .L2 met the requirements of the Haglunds-benison HFO specification, the Cincinnati Milacron P68, P69 and P70 specifications, and the Vickers vane pump specification.
In yet another experiment, blend 13 was formed by blending the additive components of blend 12 in the same concentrations as blend 12 with rape seed oil. Blend 13 gave the same F:~G, IP135B, and clarity results as blend 11.
In further test=ing blend 13 was found to satisfy the pump test requirements of the Haglunds-benison HFO
specification, as well as the Cincinnati Milacron thermal stability test produced "A". In this latter test procedure, a copper rod and an iron rod are kept in contact with each other under the surface of 200 milliliters of test oil in a beaker for 7 days at a constant temperature of 135°C. On completion of the test it was found that passing ratings were achieved relative to sludge formation, iron rod performance and weight change of the copper rod.
This invention relates to lubricant compositions, and more especially to lubricant compositions which can be used as hydraulic fluids.
Lubricant compositions normally contain a variety of additives incorporated to improve the performance of the lubricant in the environment in which it is to be used.
Such additives often contain transition metals. As is well known, there is now a general need, for environmental reasons, to reduce the use of transition metals which are frequently toxic. For example, lubricants used as hydraulic fluids often contain, as an anti-wear additive, a zinc dialkyl dithiophosphate (a so-called "ZDDP"). It is desirable to be able to provide hydraulic fluids which are zinc free: This is especially true where the hydraulic fluid is to be used in agriculture or arbariculture where spillage of the fluid onto cultivated land may occur and cause pollution of the land and of any drainage or river system connected with it.
It is also desirable on practical grounds to be able to provide an additive system which is suitable for use in all types of hydraulic fluid irrespective of the particular equipment in which it will be used. A universal anti-wear (UAW) additive system for,. use in such hydraulic fluids must be capable of providing fluids capable of meeting the specifications of the leading hydraulic pump manufacturers, e.g. the Haglunds-benison HFO specification and the Vickers Vane pump specification. It is a further requirement for such fluids that they must meet higher than load stage 10 performance in the FZG test described in more detail below.
Hydraulic fluids incorporating ZDDPs do not always give the required performance in the FZG test.
There is therefore a need for a metal-free universal anti-wear additive system suitable for use in lubricant compositions to be used in, for example, piston and screw compressors, industrial gear systems, and, more particularly, in hydraulic fluids.
According to the present invention, a lubricant composition comprises (a) a metal~free anti°wear or load carrying additive containingsulphur and/or phosphorus, and (b) a corrosion inhibitor in the form of an amino succinate ester of formula ... ,.,.. R3R4C_COORl .
R6R~~-,CRS-CCt~R2 _ in which Rl and R2 are each alkyl of 1 to 30, preferably 1 to 12, carbon atoms, R3, R4 and R5 are each hydrogen or alkyl of 1 to 4 carbon atoms, and R6 and R~ are each.
hydrogen" alkyl or l to 30 carbon, atoms, or an aryl group derived from a saturated or u~sa~urated carboxylic acid of up to 30 carbon atoms, at least one of R6 and R~ being a said acyl group. Preferably Rl.and R2 are each alkyl of 3 to 6 carbon atoms,..e,g, isobutyl, R3, R4 and RS are each hydrogen,, and Rg and:R~ axe each alkyl of 15 to 20 carbon atoms or an acyl radical derived from a saturated or ' -3-unsaturated dicarboxylic acid containing 4 to 10 carbon atoms, e.g, octadecyl, octadecenyl, or 3-carboxy-1-oxo-2-propenyl. An especially preferred component (b) is aspartic acid, N-(3-carboxy-1-axa-2-propenyl)-N-octadecyl-bis (2-methylgropyl)ester.
The metal free, and preferably ashless, anti-wear or load carrying additive may be any one of a wide range of sulphur- and/or phosphorus-containing additives, for example a mono- and/or di-hydrocarbyl phosphate or phosphite wherein the hydrocarbyl radical is alkyl of up to l2 carbon atoms, e.g. n-butyl, iso-butyl, n-amyl, n-octyl, 2-ethylhexyl or n-dodecyl, or a mixture thereof, and amine salts of such phosphates and phosphites, for example with primary amines of 4 to 18 carbon atoms, e.g» n-butylamine, n-octylamine, tert-octyZ primary amine, n-dodecylamine, the commercially available mixture of tertiary alkyl primary amines such as Primene 81R in which the tertiary alkyl radicals contain. l2 to 14 carbon atoms each, n-octadecylamine, aleylamine, and also secondary and tertiary amines such as di-n-octylamine, and tri-n-octylamine.
Other metal-free anti-wear or load carrying additives which can be used in the compositions of the present invention are sulphurized hydrocarbyl phosphites such as mono-- and di-hydrocarbyl thiophosphates wherein the hydrocarbyl radical may be aryl, e.g, phenyl, alkylaryl, e.g. alkylphenyl in which the alkyl contains up to 12 carbon atoms, arylalkyl, or aliphatic, e.g, alkyl of up to 12 s carbon atoms. Examples of such sulphurized hydrocarbyl phosphites includes diphenylthiophosphate, dinonylphenyl thiophosphates, di-n-butyl thiophosphate, di-isobutyl thiophosphate and di-2-ethylhexyl thiophosphate. Amine salts of such thiophosphates may also be used.
The anti-wear or load-carrying additive may also be a tri-hydrocarbyl di-thiophosphate in which each hydrocarbyl group may be, for example, an aromatic, alkylaromatic, cycloaliphatic, or aliphatic radical as aforesaid, e.g.
isopropyl, n-butyl, isobutyl, n-pentyl, n=hexyl, 2-ethylhexyl or n-dodecyl. The hydrocarbyl group may also be an alkenyl or cycloalkyl radical.
Other metal free antiwear or load carrying additives which can be used in the invention are sulphurized alkenes, e.g. sulphuri,zed isobutene, containing, for example 42 to 48~.by weight of sulphur or a sulphurized carboxylic acid or ester thereof in which the acid is,,for,example a fatty acid such as oleic or linoleic acid, e.g, a sulphurized vegetable oil or animal fat such as rape seed oil or lard oil.
Suitable cammercially available sulphurised fatty ester materials of, this type. include Sulperm lOS (Keil Chemical) and EP Oil GE10 ~Hornett). These typically contain about 9.5o and about 8.5-9.5% sulphur, respectively.
Dialkylpolysulphides such as t-nonyl trisulphide or t-dodecyl pentasulphide can also be used as the anti-wear or load-carrying additive.
The sulphur or phosphorus containing anti-wear or load carrying additive is advantageously prepared in the way described in our British Patent Application No. 8829597.7.
These anti-wear or load-carrying additives are amine salts of phosphorothioic acids of formula:
_5_ (RO) 2PS0-.H~I~R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and Rl, R2 and R3 are each hydrogen or substituted or unsubstituted hydrocarbyl radicals of up to 22 carbon atoms, not more than 2 of R1, R2 and R3 being hydrogen. When produced by the pracess of the aforesaid application, such salts have a purity of at least 95~ and have little reactivity towards copper, and less than 3$ of a phosphate of formula (RO)2POH in which R is as hereinbefore defined or amine salt thereof. Preferred such amine salts are those in which R is alkyl of 3 to 8 carbon atoms or phenyl and each of R1, R2 and R3 is hydrogen or an alkyl, cycloalkyl or alkenyl radical of 4 to 22 carbon atoms, not more than 2 of Rl, R2 and R3 being hydrogen. Preferably R
is phenyl, R1 and ~2 are hydrogen, and R3 is mixed C12-C14 tertiary alkyl.
Such amine salts are made by forming a mixture of sulphur and the amine in the liquid state, adding to the mixture a phosphate ester of formula (RO)2POH in an amount at least equivalent to the amount of sulphur under conditions such that the sulphur reacts with the ester but the reaction temperature does not rise above 130oC, and then continuing the reaction untal the solid sulphur has substantially disappeared from the reaction mixture. The quantity of amine is adjusted if necessary so that the total quantity of amine is at least equivalent to the quantity of the phosphite ester.
Compatible mixtures of such anti-wear or load-carrying additives can, of course, :also be used.
The proportions of components (a) and (b) in the lubricant compositions of the invention are preferably from 0.05$ to 3$, preferably 0.1$ to 1.5$, of the antiwear or load carrying additive and from 0.002$ to 0.5~, preferably 0.05 to 0.25, by weight of the corrosion inhibitor, such percentages being by weight based on the total weight of the lubricant composition.
The lubricant composition may include as the base fluid any mineral or non-mineral oil suitable for use as a lubricant, or more especially as a hydraulic fluid. Such base stocks include paraffinic lubricating oil base stocks of mineral origin, synthetic oils such as polyalphaolefins, e.g. hydrogenated polydecene, synthetic lubricant. esters, such as dialkyl adipates and azelates (in which the alkyl groups typically have l to 20 carbon atoms each, e.g.
dioctyl azelate, dinonyl adipate, or di-2-ethylhexylazelate) and oils of biological origin including more particularly lubricant vegetable oils such as rape seed oil, jojoba oil, cotton seed oil, peanut oilyor palm oil.
It is a particular advantage of the invention that the combination of components (a) and (b) as set out above is compatible with a variety of oils of natural, especially vegetable, origin suitable for use as hydraulic fluids.
Such natural oils are biodegradable, and in conseguence,the . _7-present invention makes it possible to provide an effective hydraulic fluid based on a biodegradable base stock such as rape seed oil or jojoba oil and incorporating additives which are free from heavy metals.
When it is to be used in an acidic environment, it can be desirable to incorporate in a lubricant composition of the present invention a third component, vie. (c) an alkaline earth metal alkylbenzene sulphanate, alkyl-naphthalene sulphonate, petroleum sulphonate, alkylphenate, alkyl sulphurized phenate, or alkylsalicylate. This material is usually overbased and may also be sulphuri2ed.
A sulphurized overbased calcium alkylphenate in which the . alkyl group is paranonyl, or a calcium dinonylnaphthalene-sulphonate is preferably used. The proportion of such additional additive is usually in the range 0.005 to 0.50$
based on the total weight of the composition. Such compositions are not ashless, but they do not contain heavy metals and thus achieve one of the major objectives of the present invention.
The lubricant compositions of the present invention may incorporate other additives conventionally used in lubricants, for example:
(i) Additional corrosion inhibitors, e.g. amine salts of carboxylic acids such as octylamine octanoate, condensation products of dodecenyl succinic acid or anhydride and a fatty acid such as oleic acid with a polyamine, e.g. a polyalkylene polyamine such as -g_ triethylenetetramine, and half esters of alkenyl succinic acids in which the alkenyl radical contains 8 to 24 carbon atoms with alcohols such as polyglycols.
(ii) Ashless dispersants, especially those made by reaction of a polyolefin malefic anhydride reaction product with a polyalkylene polyamine such as triethylene tetramine or tetraethylene pentamine. In such dispersants, the polyolefin is typically polyisobutene having a number average molecular weight of 900 to 1200.
In some circumstances, it may be advantageous to boronate such ashless dispersants. While boron is non-metal, it is ash-forming and its use in the compositions of the invention is not preferred.
(iii) Antioxidants including, for example, phenolic antioxidants such as 2,6-di-tert-butylphenol, 2,6-di-tert-butyl-4-methylphenol, and 4,4°-methylenebis(2,6-di-tertbutyl-phenol), sulphurized phenolic antioxichnts such as 4,4'-thiobis(6-tent-butyl-o-cresol) and aromatic amines such as di(nonylphenyl)amine and octylated phenyl-alpha--naphthylamine., Mixtures of phenolic antioxidants and aromatic amine. antioxidants (e.g., ETHYL~ Antioxidant 728 and/or 733.wi~h Nauga;lube 438L) are preferred.
(iv) Copper deactivators, e.g. benzotriazole and its derivatives, thiadiazoles and their derivatives, ar tricr~esyl phosphate. , (v) Demulsifying agents, more particularly, surfactants which are preferably ashless, e.g. non-ionic surfactants such as polyglycols.
(vi) Viscosity index improvers, e.g.
' -9-poly(alkylmethacrylates) and olefin copolymers such as ethylene/propylene and styrene/isoprene copolymers, and dispersant viscosity index improvers such as copolymers, of an alkylmethacrylate with N-vinylpyrrolidone and olefin copolymers grafted with nitrogen-containing monomers such as diallylformamide.
(vii) Pour point depressants such as poly(alkyl-methacrylates).
(viii) Anti-foam agents,.e.g. products based on silicones and poly(alkylacrylates).
All such additional ingredients must of course be compatible with components (a) and (b) but, subject to this, they are used in the usual proportions.
The compositions of the invention are conveniently supplied to the formulator of the finished lubricant composition in the form of an additive concentrate comprising the components (A) and (B) as aforesaid, alone or preferably with a relatively small amount of suitable base oil to facilitate handling, and optionally with one or more of the additional ingredients mentioned above. In such concentrates the amounts of components (A) and (B) are proportioned such that when the concentrate is blended into a base fluid to provide a finished lubricant composition in which the concentration of component (A) is from 0.05 to 3% by weight and preferably from 0.1 to 1.5o by weight based on the total weight of the lubricant composition, the cancentration of component (B) is from 0.002 to 0.5o by weight and preferably from 0.05 to 0.25 % by weight based on the total weight of the lubricant composition. Thus the ratio of (A) to (B) in such concentrates is preferably 30:1 to 0.4:1. The proportion of component (B) in the concentrate is preferably from 0.1 to 50o by weight, especially 0.1 to 10%, and most commonly 1 to 5% by weight of the concentrate.
The following Examples illustrate the invention.
~iydraulic fluid blends were prepared using as the base stock an ISO 46 mineral base oil having a kinematic viscosity range at 40°C of from 41.4 to 50.6 cSt. The additives incorporated were as stated below. Each blend was evaluated for clarity and by the IP 1358 corrosion test.
The latter test involves stirring a mixture of 300 ml of the hydraulic fluid with 30 ml of artificial sea water at a temperature of 60°C with a steel cylinder immersed in the mixture. The test was run in duplicate for 24 hours with each blend and the immersed steel specimens were then examined for signs of rusting. For a pass, no rust must be visible on the specimen.
The blends were also examined by the FZG test (IP334/79). In this test two steel spur gears are rotated together with oil dip lubrication for a series of.l5 minute stages. The relative torque between the gears is increased by a,fixed amount after each stage and' the gears are run together. for a.given period after which they are examined for wear or damage: The result of the test is quoted in -l0A-terms of the final pass stage and the first fail stage. To be satisfactory, the pass stage must be higher than 10.
The following Tables I and II set out the compositions of the hydraulic fluids tested and the results obtained with each. Blend 4, 5, 6, 7 and 10 are in accordance with the present invention. The other blends are for comparison.
HYDRAULIC FLUID BASE OIL
Blend 1 2 3 4 5 6 Component AZ 0.07 0.07 0.07 0.07 0.07 0.1 Component A2 0.19 0.19 0.19 0.19 0.19 0.12 Component B - - - 0.02 0.02 0.015 Corrosion Inhib. D 0.065 - 0.04 0.03 0.025 0.025 Corrosion Inhib. E - 0.02 - - - -Corrosion Inhib. F - - 0.075 - - -FZG Load 12 Pass 9 Pass/Not 12 Pass 12 Pass12 Pass Stage Fail 10 FailTested IP 135 B Fail Fail Not Pass Pass Pass Test Result ModerateSevere Tested No rust No rustNo rust Rust Rust ' Clarity of Blended fluid Clear Clear Cloudy Clear Clear Clear Component AZ was the Primene 81R salt of diphenylthiophosphate.
Component A2 was a blend of 36$ di-t-nonyl polysulphide and 64$
sulphurised fatby ester Component B was aspartic acid, N-(3 carboxy-2-oxo-2-propenyl)-N-octadecyl-bis(2-methylpropyl)ester.
Corrosion Inhibitar D was a condensation product of dodecenyl succinic acid and oleic acid with a polyethylene polyamine Corrosion Inhibitor E was octylamine octanoate.
Corrosion Inhibitor F was a modified imidazoline (Monamulse CI) Blends 1-6 contained the same levels of conventional antioxidant, copper deactivator and demulse aid.
Blends 2 and 5 additionally contained a boronated polyisobutenyl succinimide ashless dispersant in conventional amount. In blend 6, component Al was prepared in the way described in British Patent Application 8829597,7 ~, l TABLE II
CONCENTRATIONS IN WT PERCENTAGE IN IS046 flYDRAULIC
FLUID BASE OIL
Blend 7 8 9 10 Component A1 0.07 0.07 0.07 0.07 Component A2 0.19 0,19 0.19 0.19 Component B 0.04 - -- 0,02 Detergent C 0.04 (C1) 0.04 (C1) 0.04 (C1) 0.0075 (C2) Corrosion Inhib.F - 0.04 - -Corrosion Inhib.G - - 0.03 -Corrosion Inhib.D 0.05 0.05 0.05 0.025 Clarity of Blended Fluid Clear Cloudy flazy Clear IP135B...Test Result Pass Pass Pass Pass FZG Load Stage Fail 11 Pass/ 11 Pass/ ll Pass/ 11 Pass/
-- 12 Fail 12 Fail 12 Fail 12 Fail Components A1, A2, B, D and F were as in Table I.
Detergent CZ was an overbased calcium sulphurised nonyl-phenate.
Detergent C2 was calcium dinonyl naphthalene sulphonate Corrosion Inhibitor G was butanedioic acid, sulpho-1,4-tridecyl ester, sodium salt.
Blends 7, 8 and 9 contained the same levels of conventional antioxidant, copper deactivator, VI improver and demulse aid.
Blend 10 similar to blends 7 to 9 but contained a boronated polybutenyl succinimide ashless dispersant in conventional amount and no VI improver.
In a furthe=r experiment, a blend 11 was made having the same composition as blend 6 except that the base oil was rape seed oil. The results in the FZG test, the IP135B
test, and the clarity of the blend were the same as those obtained with b7Lend 6.
In another experiment, a blend 12 was made having the same composition as blend 6 except that component A1 was used at a concentration of 0.11 weight percent, and component A2 was composed entirely of the sulphurised fatty ester (Sulperm lOS). Blend 12 produced the same FZG, IP135B, and clarity results as blend 6. In performance testing, blend .L2 met the requirements of the Haglunds-benison HFO specification, the Cincinnati Milacron P68, P69 and P70 specifications, and the Vickers vane pump specification.
In yet another experiment, blend 13 was formed by blending the additive components of blend 12 in the same concentrations as blend 12 with rape seed oil. Blend 13 gave the same F:~G, IP135B, and clarity results as blend 11.
In further test=ing blend 13 was found to satisfy the pump test requirements of the Haglunds-benison HFO
specification, as well as the Cincinnati Milacron thermal stability test produced "A". In this latter test procedure, a copper rod and an iron rod are kept in contact with each other under the surface of 200 milliliters of test oil in a beaker for 7 days at a constant temperature of 135°C. On completion of the test it was found that passing ratings were achieved relative to sludge formation, iron rod performance and weight change of the copper rod.
Claims (27)
1. A lubricant composition comprising (a) a metal-free anti-wear or load-carrying additive containing sulphur and/or phosphorus and (b) a corrosion inhibitor in the form of an amino succinate ester of formula in which each of R1 and R2 is alkyl of 1 to 30 carbon atoms; each of R3, R4 and R5 is selected from hydrogen and alkyl of 1 to 4 carbon atoms; and each of R6 and R7 is selected from hydrogen, alkyl of 1 to 30 carbon atoms, and an aryl group derived from a saturated or unsaturated carboxylic acid of up to 30 carbon atoms, at least one of R6 and R7 being a said acyl group.
2. A lubricant composition according to claim 1 in which, in the said amino succinate ester, R1 and R2 are each alkyl of 3 to 6 carbon atoms; R3, R4 and R5 are each hydrogen; and each of R6 and R7 is selected from alkyl of 15 to 20 carbon atoms and an acyl radical derived from a saturated or unsaturated dicarboxylic acid containing 4 to 10 carbon atoms.
3. A lubricant composition according to claim 1 wherein the corrosion inhibitor is aspartic acid, N-(3-carboxy-1-oxo-2-propenyl)-N-octadecyl-bis(2-methylpropyl) ester.
4. A lubricant composition according to claim 1 wherein the metal-free anti-wear or load-carrying additive is a mono- and/or di-hydrocarbyl phosphate or phosphate wherein the hydrocarbyl radical is alkyl of up to 12 carbon atoms or an amine salt of such a phosphate or phosphate or a mixture thereof.
5. A lubricant composition according to claim 1 wherein the metal-free anti-wear or load-carrying additive is a mono- or di-hydrocarbyl thiophosphate wherein the hydrocarbyl radical is aryl, alkylaryl, aryalkyl, or alkyl, or an amine salt thereof.
6. A lubricant composition according to claim 5 wherein the said thiophosphate is diphenylthiophosphate, dinonylphenyl thiophosphate, di-n-butyl thiophosphate, diisobutyl thiophosphate, di-2-ethylhexyl thiophosphate or a mixture thereof.
7. A lubricant composition according to claim 1 wherein the metal-free anti-wear or load-carrying additive is a tri-hydrocarbyl dithiophosphate in which each hydrocarbyl group is an aromatic, alkylaromatic, cycloaliphatic, or aliphatic radical.
8. A lubricant composition according to claim 1 wherein the anti-wear or load-carrying additive is an amine salt of a phosphorothioic acid of formula:
(RO)2PSO-HN+R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and R1, R2, and R3 are each hydrogen or a substituted or unsubstituted hydrocarbyl radical of up to 22 carbon atoms, not more than 2 of R1, R2, and R3 being hydrogen.
(RO)2PSO-HN+R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and R1, R2, and R3 are each hydrogen or a substituted or unsubstituted hydrocarbyl radical of up to 22 carbon atoms, not more than 2 of R1, R2, and R3 being hydrogen.
9. A lubricant composition according to claim 8 wherein R
is alkyl of 3 to 8 carbon atoms or phenyl and each of R1, R2, and R3 is hydrogen or an alkyl, cycloalkyl or alkenyl radical of 4 to 22 carbon atoms each, not more than two of R1, R2, and R3 being hydrogen.
is alkyl of 3 to 8 carbon atoms or phenyl and each of R1, R2, and R3 is hydrogen or an alkyl, cycloalkyl or alkenyl radical of 4 to 22 carbon atoms each, not more than two of R1, R2, and R3 being hydrogen.
10. A lubricant composition according to claim 1 wherein the anti-wear or load-carrying additive is comprised of a combination of (i) at least one metal-free anti-wear or load-carrying additive containing phosphorus and (ii) at least one metal-free anti-wear or load-carrying additive containing sulphur.
11. A lubricant composition according to claim 1 wherein the anti-wear or load-carrying additive is comprised of a combination of (i) an amine salt of a phosphorothioic acid of formula:
(RO)2PSO- HN+R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and R1, R2, and R3 are each hydrogen or a substituted or unsubstituted hydrocarbyl radical of up to 22 carbon atoms, not more than 2 of R1, R2, and R3 being hydrogen; and (ii) a sulphurized fatty acid ester.
(RO)2PSO- HN+R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and R1, R2, and R3 are each hydrogen or a substituted or unsubstituted hydrocarbyl radical of up to 22 carbon atoms, not more than 2 of R1, R2, and R3 being hydrogen; and (ii) a sulphurized fatty acid ester.
12. A lubricant composition according to claim 1 wherein the anti-wear or load-carrying additive is comprised of a combination of (i) an amine salt of a phosphorothioic acid of formula:
(RO)2PSO- HN+R1R2R3 in which the radicals R are phenyl, R1 and R2 are hydrogen and R3 is mixed C12-C14 tertiary alkyl; (ii) sulphurized fatty acid ester and (iii) dialkyl polysulfide.
(RO)2PSO- HN+R1R2R3 in which the radicals R are phenyl, R1 and R2 are hydrogen and R3 is mixed C12-C14 tertiary alkyl; (ii) sulphurized fatty acid ester and (iii) dialkyl polysulfide.
13. A lubricant composition according to claim 8 wherein the corrosion inhibitor is aspartic acid, N-(3-carboxy-1-oxo-2-propenyl)-N-octadecyl-bis(2-methylpropyl) ester.
14. A lubricant composition according to claim 10 wherein the corrosion inhibitor is aspartic acid, N-(3-carboxy-1-oxo-2-propenyl)-N-octadecyl-bis(2-methylpropyl) ester.
15. A lubricant composition according to claim 11 wherein the corrosion inhibitor is aspartic acid, N-(3-carboxy-1-oxo-2-propenyl)-N-octadecyl-bis(2-methylpropyl) ester.
16. A lubricant composition according to claim 12 wherein the corrosion inhibitor is aspartic acid, N-(3-carboxy-1-oxo-2-propenyl)-N-octadecyl-bis(2-methylpropyl) ester.
17. A lubricant composition according to claim 1 wherein the lubricant base stock is a paraffinic lubricating oil base stock of mineral origin, a synthetic polyalphaolefin, a synthetic lubricant ester or an oil of biological origin.
18. A lubricant composition according to claim 17 in which the base stock is a biodegradable vegetable oil.
19. A lubricant composition according to claim 18 in which the vegetable oil is a rape seed oil.
20. A lubricant composition according to claim 1 which contains also an alkalines earth metal alkybenzene sulphonate, alkaline earth metal alkylnaphthalene sulphonate, alkaline earth metal petroleum sulphonate, alkaline earth metal alkylphenate, alkaline earth metal alkyl sulphurized phenate or alkaline earth metal alkylsalicylate.
21. A lubricant composition according to claim 1 containing 0.1 to 1.5% by weight of the anti-wear or load-carrying additive and from 0.05 to 0.25% by weight of the corrosion inhibitor.
22. An additive concentrate comprising (a) at least one metal-free anti-wear or load-carrying additive containing sulphur and/or phosphorus and (b) a corrosion inhibitor in the form of an amino succinate ester of formula in which each of R1 and R2 is alkyl of 1 to 30 carbon atoms; each of R3, R4 and R5 is selected from hydrogen and alkyl of 1 to 4 carbon atoms; and each of R6 and R7 is selected from hydrogen, alkyl of 1 to 30 carbon atoms, and an acyl group derived from a saturated or unsaturated carboxylic acid of up to 30 carbon atoms, at least one of R6 and R7 being a said acyl group.
23. An additive concentrate according to claim 22 wherein the anti-wear or load-carrying additive comprises an amine salt of a phosphorothioic acid of formula:
(RO)2PSO- HN+R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and R1, R2, and R3 are each hydrogen or a substituted or unsubstituted hydrocarbyl radical of up to 22 carbon atoms, not more than 2 of R1, R2, and R3 being hydrogen.
(RO)2PSO- HN+R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and R1, R2, and R3 are each hydrogen or a substituted or unsubstituted hydrocarbyl radical of up to 22 carbon atoms, not more than 2 of R1, R2, and R3 being hydrogen.
24. An additive concentrate according to claim 22 wherein the anti-wear or load-carrying additive is comprised of a combination of (i) an amine salt of a phosphorothioic acid of formula:
(RO)2PSO- HN+R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and R1, R2, and R3 are each hydrogen or a substituted or unsubstituted hydrocarbyl radical of up to 22 carbon atoms, not more than 2 of R1, R2, and R3 being hydrogen;
and (ii) a sulphurized fatty acid ester.
(RO)2PSO- HN+R1R2R3 in which the radicals R are the same or different and each is a substituted or unsubstituted hydrocarbyl radical of up to 20 carbon atoms and R1, R2, and R3 are each hydrogen or a substituted or unsubstituted hydrocarbyl radical of up to 22 carbon atoms, not more than 2 of R1, R2, and R3 being hydrogen;
and (ii) a sulphurized fatty acid ester.
25. An additive concentrate according to claim 22 wherein the anti-wear or load-carrying additive is comprised of a combination of (1) an amine salt of a phosphorothioic acid of formula:
(RO) 2PSO- HN+R1R2R3 in which the radicals R are phenyl, R1 and R2 are hydrogen and R3 is mixed C12-C14 tertiary alkyl; (ii) sulphurized fatty acid ester and (iii) dialkyl polysulfide.
(RO) 2PSO- HN+R1R2R3 in which the radicals R are phenyl, R1 and R2 are hydrogen and R3 is mixed C12-C14 tertiary alkyl; (ii) sulphurized fatty acid ester and (iii) dialkyl polysulfide.
26. An additive concentrate according to claim 23 wherein the corrosion inhibitor is aspartic acid, N-(3-carboxy-1-oxo-2-propenyl)-N-octadecyl-bis(2-methylpropyl) ester.
27. An additive concentrate according to claim 25 wherein the corrosion inhibitor is aspartic acid, N-(3-carboxy-1-oxo-2-propenyl)-N-octadecyl-bis(2-methylpropyl) ester.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB898929096A GB8929096D0 (en) | 1989-12-22 | 1989-12-22 | Metal free lubricants |
GB89-29096.9 | 1989-12-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2032940A1 CA2032940A1 (en) | 1991-06-23 |
CA2032940C true CA2032940C (en) | 2000-07-18 |
Family
ID=10668441
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002032940A Expired - Fee Related CA2032940C (en) | 1989-12-22 | 1990-12-21 | Metal free lubricants |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0434464B1 (en) |
JP (1) | JP2965710B2 (en) |
CA (1) | CA2032940C (en) |
DE (1) | DE69016976T2 (en) |
ES (1) | ES2067701T3 (en) |
GB (2) | GB8929096D0 (en) |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5328619A (en) * | 1991-06-21 | 1994-07-12 | Ethyl Petroleum Additives, Inc. | Oil additive concentrates and lubricants of enhanced performance capabilities |
DE4217961A1 (en) * | 1992-05-30 | 1993-12-02 | Fuchs Petrolub Ag Oel & Chemie | Environmentally compatible and quickly biodegradable supplies for the circulation lubrication of engines and other units in vehicles and work machines |
US5275749A (en) * | 1992-11-06 | 1994-01-04 | King Industries, Inc. | N-acyl-N-hydrocarbonoxyalkyl aspartic acid esters as corrosion inhibitors |
US5658864A (en) * | 1995-03-24 | 1997-08-19 | Ethyl Corporation | Biodegradable pour point depressants for industrial fluids derived from biodegradable base oils |
GB2301113A (en) * | 1995-05-22 | 1996-11-27 | Ethyl Petroleum Additives Ltd | Extreme pressure gear lubricant |
US5750478A (en) * | 1995-12-22 | 1998-05-12 | Exxon Research And Engineering Company | High load-carrying turbo oils containing amine phosphate and sulfurized fatty acid |
US5679627A (en) | 1995-12-22 | 1997-10-21 | Exxon Research & Engineering Company | High-load carrying turbo oils containing amine phosphate and a sulfur containing carboxylic acid (law348) |
US5587355A (en) * | 1995-12-22 | 1996-12-24 | Exxon Research And Engineering Company | High load-carrying turbo oils containing amine phosphate and thiophene carboxylic acid derivatives |
US5582760A (en) * | 1995-12-22 | 1996-12-10 | Exxon Research And Engineering Company | High load-carrying turbo oils containing amine phosphate and alkylthiosuccinic acid |
US5801130A (en) * | 1995-12-22 | 1998-09-01 | Exxon Research And Engineering Company | High load-carrying turbo oils containing amine phosphate and dimercaptothiadiazole derivatives |
US5585029A (en) * | 1995-12-22 | 1996-12-17 | Exxon Research And Engineering Company | High load-carrying turbo oils containing amine phosphate and 2-alkylthio-1,3,4-thiadiazole-5-alkanoic acid |
US5714441A (en) * | 1996-07-12 | 1998-02-03 | Exxon Research And Engineering Company | Additive combination to reduce deposit forming tendencies and improve antioxidancy of aviation turbine oils |
US5856280A (en) * | 1996-07-12 | 1999-01-05 | Exxon Research And Engineering Company | Sulfur-containing carboxylic acid derivatives to reduce deposit forming tendencies and improve antioxidancy of aviation turbine oils |
CA2225352C (en) * | 1998-01-30 | 2003-10-21 | Nam Fong Han | Vegetable derived petroleum jelly replacement |
GB9810869D0 (en) * | 1998-05-20 | 1998-07-22 | Ass Octel | Biodegradable corrosion inhibitors |
KR100697579B1 (en) * | 1999-04-14 | 2007-03-22 | 쉘 인터내셔날 리서치 마챠피즈 비.브이. | Hydraulic fluid |
FR2806094A1 (en) * | 2000-03-09 | 2001-09-14 | Ceca Sa | Multipurpose lubricant compounds containing phosphorous and sulfur compounds, useful in industrial lubricating formulations for lubrication of machinery and as metal working lubricants |
JP4608129B2 (en) * | 2001-05-11 | 2011-01-05 | 昭和シェル石油株式会社 | Lubricating oil composition |
BR0314307A (en) * | 2002-09-19 | 2005-07-05 | Ciba Sc Holding Ag | Succinic Acid Semi-Amides As Anticorrosive Agents |
JP2004217797A (en) * | 2003-01-15 | 2004-08-05 | Ethyl Japan Kk | Gear oil composition having long life and excellent thermal stability |
JP5426829B2 (en) * | 2007-02-07 | 2014-02-26 | 昭和シェル石油株式会社 | Lubricating oil composition for chattering, vibration and squealing of hydraulic cylinders |
JP5475981B2 (en) * | 2007-12-12 | 2014-04-16 | 昭和シェル石油株式会社 | Lubricating oil composition |
JP5475984B2 (en) * | 2007-12-12 | 2014-04-16 | 昭和シェル石油株式会社 | Lubricating oil composition |
WO2009074664A1 (en) * | 2007-12-12 | 2009-06-18 | Shell Internationale Research Maatschappij B.V. | Lubricating oil composition |
JP5184068B2 (en) * | 2007-12-13 | 2013-04-17 | Jx日鉱日石エネルギー株式会社 | Flame retardant hydraulic fluid composition |
JPWO2009139433A1 (en) * | 2008-05-14 | 2011-09-22 | 協和発酵ケミカル株式会社 | Oil additive and lubricating oil containing the same |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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GB1542113A (en) * | 1976-06-11 | 1979-03-14 | Lubrizol Corp | Sulphurized unsaturated compounds and their use as lubricant additives |
US4116877A (en) * | 1977-07-08 | 1978-09-26 | Exxon Research & Engineering Co. | Elastomer compatible seal swell additive for automatic transmission fluids, power transmission fluids and hydraulic steering applications |
GB2115000B (en) * | 1982-02-17 | 1985-02-06 | Shell Int Research | Lubricating oils and hydraulic fluids |
DE3789382T2 (en) * | 1986-06-13 | 1994-10-20 | Lubrizol Corp | LUBRICANT CONTAINING PHOSPHORUS AND FUNCTIONAL FLUID PREPARATIONS. |
-
1989
- 1989-12-22 GB GB898929096A patent/GB8929096D0/en active Pending
-
1990
- 1990-12-21 JP JP2412602A patent/JP2965710B2/en not_active Expired - Fee Related
- 1990-12-21 GB GB9027874A patent/GB2239257B/en not_active Expired - Lifetime
- 1990-12-21 ES ES90314188T patent/ES2067701T3/en not_active Expired - Lifetime
- 1990-12-21 EP EP90314188A patent/EP0434464B1/en not_active Expired - Lifetime
- 1990-12-21 CA CA002032940A patent/CA2032940C/en not_active Expired - Fee Related
- 1990-12-21 DE DE69016976T patent/DE69016976T2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
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CA2032940A1 (en) | 1991-06-23 |
JPH04114097A (en) | 1992-04-15 |
DE69016976T2 (en) | 1995-06-22 |
GB9027874D0 (en) | 1991-02-13 |
GB8929096D0 (en) | 1990-02-28 |
GB2239257B (en) | 1994-01-19 |
EP0434464B1 (en) | 1995-02-15 |
EP0434464A1 (en) | 1991-06-26 |
GB2239257A (en) | 1991-06-26 |
DE69016976D1 (en) | 1995-03-23 |
JP2965710B2 (en) | 1999-10-18 |
ES2067701T3 (en) | 1995-04-01 |
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