EP1195426B1 - Lubricating oil composition for gas-fuelled engines - Google Patents
Lubricating oil composition for gas-fuelled engines Download PDFInfo
- Publication number
- EP1195426B1 EP1195426B1 EP01203645A EP01203645A EP1195426B1 EP 1195426 B1 EP1195426 B1 EP 1195426B1 EP 01203645 A EP01203645 A EP 01203645A EP 01203645 A EP01203645 A EP 01203645A EP 1195426 B1 EP1195426 B1 EP 1195426B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- tbn
- gas
- lubricating oil
- salicylate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 45
- 239000010687 lubricating oil Substances 0.000 title claims description 30
- 239000000654 additive Substances 0.000 claims description 31
- 239000003599 detergent Substances 0.000 claims description 25
- 229910052751 metal Inorganic materials 0.000 claims description 19
- 239000002184 metal Substances 0.000 claims description 19
- 230000000996 additive effect Effects 0.000 claims description 18
- 229960001860 salicylate Drugs 0.000 claims description 17
- 239000002270 dispersing agent Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 239000011575 calcium Substances 0.000 claims description 14
- 239000003921 oil Substances 0.000 claims description 13
- 229910052791 calcium Inorganic materials 0.000 claims description 12
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 claims description 11
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 10
- 230000001050 lubricating effect Effects 0.000 claims description 9
- 230000003647 oxidation Effects 0.000 claims description 8
- 238000007254 oxidation reaction Methods 0.000 claims description 8
- 150000003873 salicylate salts Chemical class 0.000 claims description 8
- 239000004094 surface-active agent Substances 0.000 claims description 8
- 239000007866 anti-wear additive Substances 0.000 claims description 7
- 239000003963 antioxidant agent Substances 0.000 claims description 7
- 235000006708 antioxidants Nutrition 0.000 claims description 7
- AVVIDTZRJBSXML-UHFFFAOYSA-L calcium;2-carboxyphenolate;dihydrate Chemical compound O.O.[Ca+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O AVVIDTZRJBSXML-UHFFFAOYSA-L 0.000 claims description 5
- ZMRQTIAUOLVKOX-UHFFFAOYSA-L calcium;diphenoxide Chemical compound [Ca+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 ZMRQTIAUOLVKOX-UHFFFAOYSA-L 0.000 claims description 5
- 238000006396 nitration reaction Methods 0.000 claims description 5
- 238000002485 combustion reaction Methods 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 3
- 230000003078 antioxidant effect Effects 0.000 claims description 3
- 239000012141 concentrate Substances 0.000 claims description 2
- 230000002708 enhancing effect Effects 0.000 claims description 2
- 239000002530 phenolic antioxidant Substances 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 description 14
- 125000000217 alkyl group Chemical group 0.000 description 12
- -1 alkaline earth metal salt Chemical class 0.000 description 10
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 8
- 239000000314 lubricant Substances 0.000 description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
- 239000002199 base oil Substances 0.000 description 7
- 239000002585 base Substances 0.000 description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 description 6
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 5
- 239000011701 zinc Substances 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000003345 natural gas Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 3
- 238000005461 lubrication Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- 229960004889 salicylic acid Drugs 0.000 description 3
- 150000003870 salicylic acids Chemical class 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 150000003752 zinc compounds Chemical class 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000010705 motor oil Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 229960002317 succinimide Drugs 0.000 description 2
- 239000010689 synthetic lubricating oil Substances 0.000 description 2
- 150000003751 zinc Chemical class 0.000 description 2
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- KDUGNDDZXPJVCS-UHFFFAOYSA-N 6-oxo-6-tridecoxyhexanoic acid Chemical compound CCCCCCCCCCCCCOC(=O)CCCCC(O)=O KDUGNDDZXPJVCS-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- NEHDRDVHPTWWFG-UHFFFAOYSA-N Dioctyl hexanedioate Chemical compound CCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCC NEHDRDVHPTWWFG-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 238000007065 Kolbe-Schmitt synthesis reaction Methods 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000021523 carboxylation Effects 0.000 description 1
- 238000006473 carboxylation reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000002704 decyl group Chemical group [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])* 0.000 description 1
- 125000005266 diarylamine group Chemical group 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- MIMDHDXOBDPUQW-UHFFFAOYSA-N dioctyl decanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCC MIMDHDXOBDPUQW-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000013020 final formulation Substances 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 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
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 150000003336 secondary aromatic amines Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000004611 spectroscopical analysis 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
- 239000000126 substance Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000002966 varnish Substances 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
- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
-
- 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
- C10M129/14—Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring containing at least 2 hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/48—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring
- C10M129/54—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring containing hydroxy groups
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/52—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
- C10M133/56—Amides; Imides
-
- 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
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
- C10M137/04—Phosphate esters
- C10M137/10—Thio derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
- C10M159/22—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing phenol radicals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
- C10M159/24—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing sulfonic radicals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/251—Alcohol-fuelled engines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
- C10N2040/26—Two-strokes or two-cycle engines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
- C10N2040/28—Rotary engines
Definitions
- This invention relates to gas-fuelled engine lubrication.
- Gas-fuelled engines sometimes referred to as gas-fired engines or merely gas engines, are known and may be used in the oil and gas industry, for example, to drive pumping stations of natural gas pipelines, blowers and generators in purification plants and on gas tankers, to compress natural gas at well heads and along pipe lines and to produce electric power in fit-for-purpose plants.
- Their design may be two- or four-stroke, spark-ignited or compression-ignited, though four-stroke compression-ignited designs constitute a large percentage.
- Natural gas constitutes a typical fuel.
- US-A-5 726 133 describes a way of meeting the above problems by using, in a natural gas engine oil, an additive mixture comprising a mixture of detergents comprising at least one first alkali or alkaline earth metal salt or mixture thereof of TBN of 250 and less, and at least one second alkali or alkaline earth metal salt or mixture thereof which is more neutral than the first salt.
- EP-A-0 860 495 describes a lubricating oil composition stated to be excellent for NOx oxidation resistance and thermal oxidation resistance and suitable as a long-life engine oil for gas engine heat pumps.
- the composition includes a metal salicylate having a TBN of from 100 to 195, and optionally includes a metal phenate having a TBN of from 100 to 300.
- the present invention meets this desire, as evidenced by and in the examples hereof, by using, as a first detergent, a salicylate having a TBN of 95 or less and a second detergent having a TBN of greater than 250.
- US 5,906,969 discloses lubricating oils for improving the fuel economy of internal combustion engines.
- a first aspect of the present invention is a gas-fuelled engine lubricating oil composition having a TBN in the range of 2 to 20 comprising:
- a second aspect of the present invention is a method of lubricating a gas-fuelled internal combustion engine, the method comprising operating the engine and lubricating it with the composition defined above according to the first aspect of the invention.
- a third aspect of the present invention is a method for enhancing the resistance of a gas-fuelled lubricating oil composition to oxidation and nitration, the method comprising the step of adding additives (B) to (E) as defined in the first aspect of the invention to the gas-fuelled lubricating oil composition.
- Major amount means in excess of 50 mass % of the composition.
- Minor amount means less than 50 mass % of the composition, both in respect of the stated additive and in respect of the total mass % of all the additives present in composition, reckoned as active ingredient of the additive or additives.
- TBN Total Base Number
- the TBN of the lubricant composition is in the range of from 2 to 20, such as from 2.5 to 20, preferably from 6.5 to 20, more preferably from 6.5 to 15.
- the oil of lubricating viscosity may be any oil suitable for the lubrication of a gas-fuelled engine.
- the lubricating oil may suitably be an animal, a vegetable or a mineral oil.
- the lubricating oil is a petroleum-derived lubricating oil, such as a naphthenic base, paraffinic base or mixed base oil.
- the lubricating oil may be a synthetic lubricating oil.
- Suitable synthetic lubricating oils include synthetic ester lubricating oils, which oils include diesters such as di-octyl adipate, di-octyl sebacate and tridecyl adipate, or polymeric hydrocarbon lubricating oils, for example liquid polyisobutene and poly-alpha olefins. Commonly, a mineral oil is employed.
- the lubricating oil may generally comprise greater than 60, typically greater than 70, mass % of the composition, and typically have a kinematic viscosity at 100°C of from 2 to 40, for example for 3 to 15, mm 2 s -1 and a viscosity index of from 80 to 100, for example from 90 to 95.
- hydrocracked oils Another class of lubricating oils is hydrocracked oils, where the refining process further breaks down the middle and heavy distillate fractions in the presence of hydrogen at high temperatures and moderate pressures.
- Hydrocracked oils typically have a kinematic viscosity at 100°C of from 2 to 40, for example from 3 to 15, mm 2 s -1 and a viscosity index typically in the range of from 100 to 110, for example from 105 to 108.
- the oil may include 'brightstock' which refers to base oils which are solvent-extracted, de-asphalted products from vacuum residuum generally having a kinematic viscosity at 100°C of from 28 to 36 mm 2 s -1 and are typically used in a proportion of less than 30, preferably less than 20, more preferably less than 15, most preferably less than 10, such as less than 5, mass %, based on the mass of the composition.
- 'brightstock' refers to base oils which are solvent-extracted, de-asphalted products from vacuum residuum generally having a kinematic viscosity at 100°C of from 28 to 36 mm 2 s -1 and are typically used in a proportion of less than 30, preferably less than 20, more preferably less than 15, most preferably less than 10, such as less than 5, mass %, based on the mass of the composition.
- a detergent is an additive that reduces formation of piston deposits, for example high-temperature varnish and lacquer deposits, in engines; it has acid-neutralising properties and is capable of keeping finely divided solids in suspension. It is based on metal "soaps", that is metal salts of acidic organic compounds, sometimes referred to as surfactants, which, in respect of (B), is salicylic acid.
- the detergent comprises a polar head with a long hydrophobic tail, the polar head comprises a metal salt of the salicylic acid.
- Large amounts of a metal base are included by reacting an excess of a metal compound, such as an oxide or hydroxide, with an acidic gas such as carbon dioxide to give an overbased detergent which comprises neutralised detergent as the outer layer of a metal base (e.g. carbonate) micelle.
- the metal may be an alkali or alkaline earth metal, e.g., sodium, potassium, lithium, calcium, and magnesium. Calcium is preferred.
- Surfactants for the surfactant system of the overbased metal detergents contain at least one hydrocarbyl group, for example, as a substituent on an aromatic ring.
- hydrocarbyl as used herein means that the group concerned is primarily composed of hydrogen and carbon atoms and is bonded to the remainder of the molecule via a carbon atom, but does not exclude the presence of other atoms or groups in a proportion insufficient to detract from the substantially hydrocarbon characteristics of the group.
- hydrocarbyl groups in surfactants for use in accordance with the invention are aliphatic groups, preferably alkyl or alkylene groups, especially alkyl groups, which may be linear or branched. The total number of carbon atoms in the surfactants should be at least sufficient to impact the desired oil-solubility.
- the salicylates may be non-sulfurized or sulfurized, and may be chemically modified and/or contain additional substitutents.
- Processes for sulfurizing a hydrocarbyl-substituted salicylic acid are well known to those skilled in the art.
- Salicylic acids are typically prepared by the carboxylation, by the Kolbe-Schmitt process, of phenoxides, and in that case, will generally be obtained, normally in a diluent, in admixture with uncarboxylated phenol.
- Preferred substituents in oil-soluble salicylic acids from which the salicylates may be derived are alkyl substituents.
- the alkyl groups advantageously contain 5 to 100, preferably 9 to 30, especially 14 to 20, carbon atoms. Where there are more than one alkyl groups, the average number of carbon atoms in all of the alkyl groups is preferably at least 9 to ensure adequate oil-solubility.
- the gas-fuelled engine lubricating oil composition preferably includes only one metal hydrocarbyl-substituted salicylate detergent having a TBN of 95 or less, component (B).
- the salicylate may be used in a proportion in the range of 0.5 to 30, preferably 2 to 15 or to 20, mass % based on the mass of the lubricating oil composition.
- Component (C) is one or more calcium salicylate, phenate or complex detergents having a TBN of greater than 250.
- Complex detergents comprise an overbased mixture of at least two calcium surfactants, such as a calcium alkyl phenate and a calcium alkyl salicylate.
- a complex detergent is a hybrid material in which the surfactant groups, e.g. phenate and salicylate, are incorporated during the overbasing process. Examples of complex detergents are described in the art.
- Another example of a detergent that may be used comprises a sulfurized and then overbased mixture of a calcium alkyl phenate and a calcium alkyl salicylate such as described in EP-A-750,659 , for example as:
- the calcium detergents (C) have a TBN in the range of 250 to 500, more preferably 260 to 400.
- a dispersant is an additive for a lubricating composition whose primary function is to hold solid and liquid contaminants in suspension, thereby passivating them and reducing engine deposits at the same time as reducing sludge depositions.
- a dispersant maintains in suspension oil-insoluble substances that result from oxidation during use of the lubricating oil, thus preventing sludge flocculation and precipitation or deposition on metal parts of the engine.
- Ashless dispersants comprise a long chain hydrocarbon with a polar head, the polarity being derived from inclusion of, e.g. an O, P or N atom.
- the hydrocarbon is an oleophilic group that confers oil-solubility, having for example 40 to 500 carbon atoms.
- ashless dispersants may comprise an oil-soluble polymeric hydrocarbon backbone having functional groups that are capable of associating with particles to be dispersed.
- ashless dispersants are succinimides, e.g. polyisobutene succinic anhydride; and polyamine condensation products that may be borated or unborated.
- the antiwear additives may be metallic or non-metallic, preferably the former.
- Dihydrocarbly dithiophosphate metal salts are examples of the anti-wear additives used in the present invention.
- the metal in the dihydrocarbyl dithiophosphate metal may be an alkali or alkaline earth metal, or aluminium, lead, tin, molybdenum, manganese, nickel or copper.
- Zinc salts are preferred, preferably in the range of 0.1 to 1.5, preferably 0.5 to 1.3, mass %, based upon the total mass of the lubricating oil composition.
- DDPA dihydrocarbyl dithiophosphoric acid
- a dithiophosphoric acid may be made by reacting mixtures of primary and secondary alcohols.
- multiple dithiophosphoric acids can be prepared comprising both hydrocarbyl groups that are entirely secondary and hydrocarbyl groups that are entirely primary.
- any basic or neutral zinc compound may be used but the oxides, hydroxides and carbonates are most generally employed. Commercial additives frequently contain an excess of zinc due to use of an excess of the basic zinc compound in the neutralisation reaction.
- the preferred zinc dihydrocarbyl dithiophosphates are oil-soluble salts of dihydrocarbyl dithiophosphoric acids and may be represented by the following formula: [(RO) (R'O) P(S)S] 2 Zn where R and R' may be the same or different hydrocarbyl radicals containing from 1 to 18, preferably 2 to 12, carbon atoms and including radicals such as alkyl, alkenyl, aryl, arylalkyl, alkaryl and cycloaliphatic radicals. Particularly preferred as R and R' groups are alkyl groups of 2 to 8 carbon atoms.
- the radicals may, for example, be ethyl, n-propyl, I-propyl, n-butyl, I-butyl, sec-butyl, amyl, n-hexyl, I-hexyl, n-octyl, decyl, dodecyl, octadecyl, 2-ethylehexyl, phenyl, butylphenyl, cyclohexyl, methylcyclopentyl, propenyl, butenyl.
- the total number of carbon atoms (i.e. in R and R 1 ) in the dithiophoshoric acid will generally be 5 or greater.
- the zinc dihydrocarbyl dithiophosphate can therefore comprise zinc dialkyl dithiophosphates.
- composition of the present invention may, optionally, have further added there-to in a minor amount (F) one or more antioxidants as discussed in further detail below.
- amines or phenolic may be amines or phenolic.
- secondary aromatic amines such as diarylamines, for example diphenylamines wherein each phenyl group is alkyl-substituted with an alkyl group having 4 to 9 carbon atoms.
- anti-oxidants there may be mentioned hindered phenols, including mono-phenols and bis-phenols.
- the anti-oxidant if present, is provided in the composition in an amount of up to 3 mass %.
- additives such as pour point depressants, anti-foamants, and/or demulsifiers may be provided, if necessary.
- additives (B) to (E), and (F) if provided can be added simultaneously to the base oil to form the lubricating oil composition. Dissolution of the additive package(s) into the lubricating oil may be facilitated by solvents and by mixing accompanied with mild heating, but this is not essential.
- the additive package(s) will typically be formulated to contain the additive(s) in proper amounts to provide the desired concentration, and/or to carry out the intended function in the final formulation when the additive package(s) is/are combined with a predetermined amount of base lubricant.
- additives (B) to (E), and (F) if provided, in accordance with the present invention may be admixed with small amounts of base oil or other compatible solvents together with other desirable additives to form additive packages containing active ingredients in an amount, based on the additive package, of, for example, from 2.5 to 90, preferably from 5 to 75, most preferably from 8 to 60, mass % of additives in the appropriate proportions, the remainder being base oil.
- the final formulations may typically contain about 5 to 40 mass % of the additive packages(s), the remainder being base oil.
- 'active ingredient' refers to the additive material that is not diluent.
- 'oil-soluble' or 'oil-dispersable' do not necessarily indicate that the compounds or additives are soluble, dissolvable, miscible or capable of being suspended in the oil in all proportions. These do mean, however, that they are, for instance, soluble or stably dispersible in oil to an extent sufficient to exert their intended effect in the environment in which the oil is employed. Moreover, the additional incorporation of other additives may also permit incorporation of higher levels of a particular additive, if desired.
- the lubricant compositions of this invention comprise defined individual (i.e. separate) components that may or may not remain the same chemically before and after mixing.
- Gas-fuelled engine lubricating oil compositions of the invention were prepared by blending methods known in the art. Their compositions were as follows: COMPONENTS Example 1 Example 2 (B) Ca salicylate, TBN 65 3.46 3.85 (C) Ca salicylate, TBN 281 0.35 0.39 (D) Borated succinimide dispersant 3.41 3.80 Unborated succinimide dispersant 2.58 2.88 (E) ZDDP anti-wear additive 0.26 0.29 (F) Diphenylamine anti-oxidant 0.35 0.39 (A) Base Oil Balance Balance TBN 7.1 8 Ash (sulfated) (%) 0.45 0.50 (Antifoams were also present)
- Example A As comparison gas-fuelled engine lubricating oil compositions (Examples A and B), there were used commercially available lubricating oils, the detergency of each of which was phenate-based and was salicylate-free.
- Example A had a TBN of 5.2 and 0.45% sulfated ash and Example B had a TBN of 8.8 and 0.80% sulfated ash.
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Description
- This invention relates to gas-fuelled engine lubrication.
- Gas-fuelled engines, sometimes referred to as gas-fired engines or merely gas engines, are known and may be used in the oil and gas industry, for example, to drive pumping stations of natural gas pipelines, blowers and generators in purification plants and on gas tankers, to compress natural gas at well heads and along pipe lines and to produce electric power in fit-for-purpose plants. Their design may be two- or four-stroke, spark-ignited or compression-ignited, though four-stroke compression-ignited designs constitute a large percentage. Natural gas constitutes a typical fuel.
- Problems in their lubrication are firstly, that the lubricant is subjected to sustained high temperatures leading to its oxidation, and secondly, that the engines emit relatively high quantities of oxides of nitrogen, leading to nitration of the lubricant. These problems reduce the working life of the lubricant.
-
US-A-5 726 133 describes a way of meeting the above problems by using, in a natural gas engine oil, an additive mixture comprising a mixture of detergents comprising at least one first alkali or alkaline earth metal salt or mixture thereof of TBN of 250 and less, and at least one second alkali or alkaline earth metal salt or mixture thereof which is more neutral than the first salt. -
EP-A-0 860 495 describes a lubricating oil composition stated to be excellent for NOx oxidation resistance and thermal oxidation resistance and suitable as a long-life engine oil for gas engine heat pumps. The composition includes a metal salicylate having a TBN of from 100 to 195, and optionally includes a metal phenate having a TBN of from 100 to 300. - There is, however, a desire to further improve the lubricant performance in the above respects, for example to enable the interval between lubricant changes to be extended.
- The present invention meets this desire, as evidenced by and in the examples hereof, by using, as a first detergent, a salicylate having a TBN of 95 or less and a second detergent having a TBN of greater than 250.
-
US 5,906,969 discloses lubricating oils for improving the fuel economy of internal combustion engines. - Accordingly, a first aspect of the present invention is a gas-fuelled engine lubricating oil composition having a TBN in the range of 2 to 20 comprising:
- (A) an oil of lubricating viscosity, in a major amount; and added thereto, in respective minor amounts:
- (B) one or more metal hydrocarbyl-substituted salicylate detergents having a TBN of 95 or less, preferably 85 or less, more preferably 75 or less;
- (C) one or more calcium salicylate, phenate or complex detergents having a TBN of greater than 250, preferably greater than 265, more preferably greater than 275;
- (D) one or more dispersants, such as an ashless dispersant; and
- (E) preferably one or more anti-wear additives.
- A second aspect of the present invention is a method of lubricating a gas-fuelled internal combustion engine, the method comprising operating the engine and lubricating it with the composition defined above according to the first aspect of the invention.
- A third aspect of the present invention is a method for enhancing the resistance of a gas-fuelled lubricating oil composition to oxidation and nitration, the method comprising the step of adding additives (B) to (E) as defined in the first aspect of the invention to the gas-fuelled lubricating oil composition.
- "Major amount" means in excess of 50 mass % of the composition.
- "Minor amount" means less than 50 mass % of the composition, both in respect of the stated additive and in respect of the total mass % of all the additives present in composition, reckoned as active ingredient of the additive or additives.
- "Comprises or comprising" or cognate words is taken to specify the presence of stated features, steps, integers or components, but does not preclude the presence or addition of one or more other features, steps, integer components or groups thereof.
- "TBN" (Total Base Number) is as measured by ASTM D2896.
- Unless otherwise started, all proportions are expressed as mass % active ingredient, i.e. as if solvent or diluent or other inert material were absent.
- The features of the invention will now be discussed in more detail below.
- Preferably, the TBN of the lubricant composition is in the range of from 2 to 20, such as from 2.5 to 20, preferably from 6.5 to 20, more preferably from 6.5 to 15.
- The oil of lubricating viscosity (sometimes referred to as lubricating oil) may be any oil suitable for the lubrication of a gas-fuelled engine. The lubricating oil may suitably be an animal, a vegetable or a mineral oil. Suitably the lubricating oil is a petroleum-derived lubricating oil, such as a naphthenic base, paraffinic base or mixed base oil. Alternatively, the lubricating oil may be a synthetic lubricating oil. Suitable synthetic lubricating oils include synthetic ester lubricating oils, which oils include diesters such as di-octyl adipate, di-octyl sebacate and tridecyl adipate, or polymeric hydrocarbon lubricating oils, for example liquid polyisobutene and poly-alpha olefins. Commonly, a mineral oil is employed. The lubricating oil may generally comprise greater than 60, typically greater than 70, mass % of the composition, and typically have a kinematic viscosity at 100°C of from 2 to 40, for example for 3 to 15, mm2s-1 and a viscosity index of from 80 to 100, for example from 90 to 95.
- Another class of lubricating oils is hydrocracked oils, where the refining process further breaks down the middle and heavy distillate fractions in the presence of hydrogen at high temperatures and moderate pressures. Hydrocracked oils typically have a kinematic viscosity at 100°C of from 2 to 40, for example from 3 to 15, mm2s-1 and a viscosity index typically in the range of from 100 to 110, for example from 105 to 108.
- The oil may include 'brightstock' which refers to base oils which are solvent-extracted, de-asphalted products from vacuum residuum generally having a kinematic viscosity at 100°C of from 28 to 36 mm2s-1 and are typically used in a proportion of less than 30, preferably less than 20, more preferably less than 15, most preferably less than 10, such as less than 5, mass %, based on the mass of the composition.
- A detergent is an additive that reduces formation of piston deposits, for example high-temperature varnish and lacquer deposits, in engines; it has acid-neutralising properties and is capable of keeping finely divided solids in suspension. It is based on metal "soaps", that is metal salts of acidic organic compounds, sometimes referred to as surfactants, which, in respect of (B), is salicylic acid.
- The detergent comprises a polar head with a long hydrophobic tail, the polar head comprises a metal salt of the salicylic acid. Large amounts of a metal base are included by reacting an excess of a metal compound, such as an oxide or hydroxide, with an acidic gas such as carbon dioxide to give an overbased detergent which comprises neutralised detergent as the outer layer of a metal base (e.g. carbonate) micelle.
- The metal may be an alkali or alkaline earth metal, e.g., sodium, potassium, lithium, calcium, and magnesium. Calcium is preferred.
- Surfactants for the surfactant system of the overbased metal detergents contain at least one hydrocarbyl group, for example, as a substituent on an aromatic ring. The term "hydrocarbyl" as used herein means that the group concerned is primarily composed of hydrogen and carbon atoms and is bonded to the remainder of the molecule via a carbon atom, but does not exclude the presence of other atoms or groups in a proportion insufficient to detract from the substantially hydrocarbon characteristics of the group. Advantageously, hydrocarbyl groups in surfactants for use in accordance with the invention are aliphatic groups, preferably alkyl or alkylene groups, especially alkyl groups, which may be linear or branched. The total number of carbon atoms in the surfactants should be at least sufficient to impact the desired oil-solubility.
- The salicylates may be non-sulfurized or sulfurized, and may be chemically modified and/or contain additional substitutents. Processes for sulfurizing a hydrocarbyl-substituted salicylic acid are well known to those skilled in the art. Salicylic acids are typically prepared by the carboxylation, by the Kolbe-Schmitt process, of phenoxides, and in that case, will generally be obtained, normally in a diluent, in admixture with uncarboxylated phenol.
- Preferred substituents in oil-soluble salicylic acids from which the salicylates may be derived are alkyl substituents. In alkyl-substituted salicylic acids, the alkyl groups advantageously contain 5 to 100, preferably 9 to 30, especially 14 to 20, carbon atoms. Where there are more than one alkyl groups, the average number of carbon atoms in all of the alkyl groups is preferably at least 9 to ensure adequate oil-solubility.
- The gas-fuelled engine lubricating oil composition preferably includes only one metal hydrocarbyl-substituted salicylate detergent having a TBN of 95 or less, component (B).
- The salicylate may be used in a proportion in the range of 0.5 to 30, preferably 2 to 15 or to 20, mass % based on the mass of the lubricating oil composition.
- Component (C) is one or more calcium salicylate, phenate or complex detergents having a TBN of greater than 250.
- Complex detergents comprise an overbased mixture of at least two calcium surfactants, such as a calcium alkyl phenate and a calcium alkyl salicylate. Such a complex detergent is a hybrid material in which the surfactant groups, e.g. phenate and salicylate, are incorporated during the overbasing process.
Examples of complex detergents are described in the art. - Another example of a detergent that may be used comprises a sulfurized and then overbased mixture of a calcium alkyl phenate and a calcium alkyl salicylate such as described in
EP-A-750,659 - a detergent-dispersant additive for lubricating oil of the sulfurised and superalkalinised, alkaline earth alkylsalicylate-alkylphenate type, characterised in that:
- (a) the alkyl substituents of the said alkylsalicylate-alkylphenate are in a proportion of at least 35 wt.% and at most 85 wt.% of linear alkyl in which the number of carbon atoms is between 12 and 40, preferably between 18 and 30 carbon atoms, with a maximum of 65 wt.% of branched alkyl in which the number of carbon atoms is between 9 and 24 and preferably 12 carbon atoms;
- (b) the proportion of alkylsalicylate in the alkylsalicylate-alkylphenate mixture is at least 22 mole % and preferably at least 25 mole %, and
- (c) the molar proportion of alkaline in the alkylsalicylate-alkylphenate as a whole is between 1.0 and 3.5.
- Preferably, the calcium detergents (C) have a TBN in the range of 250 to 500, more preferably 260 to 400.
- A dispersant is an additive for a lubricating composition whose primary function is to hold solid and liquid contaminants in suspension, thereby passivating them and reducing engine deposits at the same time as reducing sludge depositions. Thus, for example, a dispersant maintains in suspension oil-insoluble substances that result from oxidation during use of the lubricating oil, thus preventing sludge flocculation and precipitation or deposition on metal parts of the engine.
- A noteworthy class of dispersants are "ashless", meaning a non-metallic organic material that forms substantially no ash on combustion, in contrast to metal-containing, hence ash-forming, materials. Ashless dispersants comprise a long chain hydrocarbon with a polar head, the polarity being derived from inclusion of, e.g. an O, P or N atom. The hydrocarbon is an oleophilic group that confers oil-solubility, having for example 40 to 500 carbon atoms. Thus, ashless dispersants may comprise an oil-soluble polymeric hydrocarbon backbone having functional groups that are capable of associating with particles to be dispersed.
- Examples of ashless dispersants are succinimides, e.g. polyisobutene succinic anhydride; and polyamine condensation products that may be borated or unborated.
- The antiwear additives may be metallic or non-metallic, preferably the former.
- Dihydrocarbly dithiophosphate metal salts are examples of the anti-wear additives used in the present invention. The metal in the dihydrocarbyl dithiophosphate metal may be an alkali or alkaline earth metal, or aluminium, lead, tin, molybdenum, manganese, nickel or copper. Zinc salts are preferred, preferably in the range of 0.1 to 1.5, preferably 0.5 to 1.3, mass %, based upon the total mass of the lubricating oil composition. They may be prepared in accordance with known techniques by firstly forming a dihydrocarbyl dithiophosphoric acid (DDPA), usually by reaction of one or more alcohols or a phenol with P2S5 and then neutralizing the formed DDPA with a zinc compound. For example, a dithiophosphoric acid may be made by reacting mixtures of primary and secondary alcohols. Alternatively, multiple dithiophosphoric acids can be prepared comprising both hydrocarbyl groups that are entirely secondary and hydrocarbyl groups that are entirely primary. To make the zinc salt, any basic or neutral zinc compound may be used but the oxides, hydroxides and carbonates are most generally employed. Commercial additives frequently contain an excess of zinc due to use of an excess of the basic zinc compound in the neutralisation reaction.
- The preferred zinc dihydrocarbyl dithiophosphates are oil-soluble salts of dihydrocarbyl dithiophosphoric acids and may be represented by the following formula:
[(RO) (R'O) P(S)S]2 Zn
where R and R' may be the same or different hydrocarbyl radicals containing from 1 to 18, preferably 2 to 12, carbon atoms and including radicals such as alkyl, alkenyl, aryl, arylalkyl, alkaryl and cycloaliphatic radicals. Particularly preferred as R and R' groups are alkyl groups of 2 to 8 carbon atoms. Thus, the radicals may, for example, be ethyl, n-propyl, I-propyl, n-butyl, I-butyl, sec-butyl, amyl, n-hexyl, I-hexyl, n-octyl, decyl, dodecyl, octadecyl, 2-ethylehexyl, phenyl, butylphenyl, cyclohexyl, methylcyclopentyl, propenyl, butenyl. In order to obtain oil-solubility, the total number of carbon atoms (i.e. in R and R1) in the dithiophoshoric acid will generally be 5 or greater. The zinc dihydrocarbyl dithiophosphate can therefore comprise zinc dialkyl dithiophosphates. - The composition of the present invention may, optionally, have further added there-to in a minor amount (F) one or more antioxidants as discussed in further detail below.
- As stated these may be amines or phenolic. As examples of amines there may be mentioned secondary aromatic amines such as diarylamines, for example diphenylamines wherein each phenyl group is alkyl-substituted with an alkyl group having 4 to 9 carbon atoms. As examples of anti-oxidants there may be mentioned hindered phenols, including mono-phenols and bis-phenols.
- Preferably, the anti-oxidant, if present, is provided in the composition in an amount of up to 3 mass %.
- Other additives such as pour point depressants, anti-foamants, and/or demulsifiers may be provided, if necessary.
- It may be desirable, although not essential, to prepare one or more additive packages or concentrates comprising the additives, whereby additives (B) to (E), and (F) if provided, can be added simultaneously to the base oil to form the lubricating oil composition. Dissolution of the additive package(s) into the lubricating oil may be facilitated by solvents and by mixing accompanied with mild heating, but this is not essential. The additive package(s) will typically be formulated to contain the additive(s) in proper amounts to provide the desired concentration, and/or to carry out the intended function in the final formulation when the additive package(s) is/are combined with a predetermined amount of base lubricant. Thus, additives (B) to (E), and (F) if provided, in accordance with the present invention, may be admixed with small amounts of base oil or other compatible solvents together with other desirable additives to form additive packages containing active ingredients in an amount, based on the additive package, of, for example, from 2.5 to 90, preferably from 5 to 75, most preferably from 8 to 60, mass % of additives in the appropriate proportions, the remainder being base oil.
- The final formulations may typically contain about 5 to 40 mass % of the additive packages(s), the remainder being base oil.
- The term 'active ingredient' (a.i.) as used herein refers to the additive material that is not diluent.
- The terms 'oil-soluble' or 'oil-dispersable' as used herein do not necessarily indicate that the compounds or additives are soluble, dissolvable, miscible or capable of being suspended in the oil in all proportions. These do mean, however, that they are, for instance, soluble or stably dispersible in oil to an extent sufficient to exert their intended effect in the environment in which the oil is employed.
Moreover, the additional incorporation of other additives may also permit incorporation of higher levels of a particular additive, if desired. - The lubricant compositions of this invention comprise defined individual (i.e. separate) components that may or may not remain the same chemically before and after mixing.
- The present invention is illustrated by, but in no way limited to, the following examples.
- Gas-fuelled engine lubricating oil compositions of the invention were prepared by blending methods known in the art. Their compositions were as follows:
COMPONENTS Example 1 Example 2 (B) Ca salicylate, TBN 65 3.46 3.85 (C) Ca salicylate, TBN 281 0.35 0.39 (D) Borated succinimide dispersant 3.41 3.80 Unborated succinimide dispersant 2.58 2.88 (E) ZDDP anti-wear additive 0.26 0.29 (F) Diphenylamine anti-oxidant 0.35 0.39 (A) Base Oil Balance Balance TBN 7.1 8 Ash (sulfated) (%) 0.45 0.50 (Antifoams were also present) - The above figures, where appropriate, represent mass % of an additive components that, with the exception of (F), includes diluent or solvent. The figure for (F) represents active ingredient.
- As comparison gas-fuelled engine lubricating oil compositions (Examples A and B), there were used commercially available lubricating oils, the detergency of each of which was phenate-based and was salicylate-free. Example A had a TBN of 5.2 and 0.45% sulfated ash and Example B had a TBN of 8.8 and 0.80% sulfated ash.
- Samples of Examples 1, 2, A and B were each tested according to the GFC T-021-A-90 procedure, an industry standard, at 170°C for a period of 216 hours, with an intermediate sampling after 144 hours.
- The samples were analysed for:
- kinematic viscosity at 100°C (ASTM D445)
- TAN (ASTM D664)
- TBN (ASTM D2896)
- Infra-Red Oxidation and Nitration (spectroscopic method known in the art)
- The identity of the method is indicated in parentheses
- The results of the tests are summarised in the table below.
SAMPLE TEST TEST TIME (hours) (EXAMPLE REF) 0 144 216 1 VISCOSITY 14.08 15.43 17.43 2 (mm2s-1) 14.38 15.37 17.59 A 13.66 23.27 - B 14.05 18.25 26.89 1 TAN 0.59 2.02 4.14 2 (mg KOHg-1) 0.65 0.71 3.65 A 0.44 5.64 8.22 B 0.38 4.45 7.17 1 TBN 7.12 2.47 1.44 2 (mg KOHg-1) 7.96 3.08 1.75 A 5.22 0.5 0.5 B . 8.81 0.5 0.5 1 IR Oxidation 0 28.91 54.69 2 (cm-1) 0 25.00 50.78 A 0 54.41 - B 0 47.06 70.59 1 IR Nitration 0 3.13 7.81 2 (cm-1) 0 3.13 6.25 A 0 20.59 - B 0 12.50 22.79 - A dash indicates that the sample was too thick to measure. In all tests (apart from TBN), lower values indicate superior performance. Thus, the results show the superiority of Examples 1 and 2 over each of Examples A and B that lacked salicylate.
Claims (8)
- A gas-fuelled engine lubricating oil composition having a TBN in the range of 2 to 20 comprising:(A) an oil of lubricating viscosity, in a major amount; and added thereto, in respective minor amounts:(B) one or more metal hydrocarbyl-substituted salicylate detergents having a TBN of 95 or less;(C) one or more calcium salicylate, phenate or complex detergents having a TBN of greater than 250;(D) one or more dispersants, such as an ashless dispersant; and(E) preferably one or more anti-wear additives.
- The composition as claimed in claim 1, further added thereto, in a minor amount, being (F) one or more antioxidants, such as amine or phenolic anti-oxidants.
- The composition as claimed in claim 1 or claim 2, wherein the metal of the hydrocarbyl-substituted salicylate (B) is calcium.
- The composition as claimed in any of claims 1 to 3, wherein the calcium detergent (C) is a calcium hydrocarbyl-substituted salicylate or a calcium complex detergent that contains a salicylate surfactant, having a TBN in the range of 250 to 500, preferably 260 to 400.
- The composition as claimed in any of claims 2 to 4, wherein the anti-oxidant (F) is present in the composition in an amount of up to 3 mass %.
- A method of lubricating a gas-fuelled internal combustion engine comprising operating the engine and lubricating it with a composition as claimed in any of claims 1 to 5.
- A method for enhancing the resistance of a gas-fuelled lubricating oil composition to oxidation and nitration, the method comprising the step of adding the composition with additives (B) to (F) as defined in any of claims 1 to 5 to the gas-fuelled engine lubricating oil composition.
- An additive package or concentrate for a gas-fuelled engine lubricating oil composition, comprising:(B) one or more metal hydrocarbyl-substituted salicylate detergents having a TBN of 95 or less;(C) one or more calcium salicylate, phenate or complex detergents having a TBN of greater than 250;(D) one or more dispersants, such as an ashless dispersant; and(E) preferably one or more anti-wear additives.
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EP01203645A EP1195426B1 (en) | 2000-10-05 | 2001-09-24 | Lubricating oil composition for gas-fuelled engines |
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EP00121752A EP1195425A1 (en) | 2000-10-05 | 2000-10-05 | Lubricating oil composition for gas-fuelled engines |
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EP01203645A EP1195426B1 (en) | 2000-10-05 | 2001-09-24 | Lubricating oil composition for gas-fuelled engines |
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US20030191032A1 (en) * | 2002-01-31 | 2003-10-09 | Deckman Douglas E. | Mixed TBN detergents and lubricating oil compositions containing such detergents |
EP1509586B1 (en) * | 2002-05-24 | 2018-09-19 | The Lubrizol Corporation | Low ash stationary gas engine lubricant |
US20050070447A1 (en) * | 2003-09-25 | 2005-03-31 | The Lubrizol Corporation | Ashless stationary gas engine lubricant |
US20070142660A1 (en) | 2005-11-09 | 2007-06-21 | Degonia David J | Salt of a sulfur-containing, phosphorus-containing compound, and methods thereof |
US20070105729A1 (en) * | 2005-11-09 | 2007-05-10 | Chip Hewette | Gear additive composition |
US8299003B2 (en) | 2005-11-09 | 2012-10-30 | Afton Chemical Corporation | Composition comprising a sulfur-containing, phosphorus-containing compound, and/or its salt, and uses thereof |
US8680030B2 (en) | 2005-11-18 | 2014-03-25 | Exxonmobil Research And Engineering Company | Enhanced deposit control for lubricating oils used under sustained high load conditions employing glycerine derivative with a grafted hindered phenolic and/or a hindered phenolic containing a thioether group |
WO2010086365A1 (en) * | 2009-01-28 | 2010-08-05 | Shell Internationale Research Maatschappij B.V. | Lubricating composition |
US20130157910A1 (en) * | 2011-12-16 | 2013-06-20 | Chevron Oronite Company Llc | Diesel engine oils |
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JP3613530B2 (en) * | 1993-05-27 | 2005-01-26 | 東燃ゼネラル石油株式会社 | Lubricating oil composition |
GB9400417D0 (en) * | 1994-01-11 | 1994-03-09 | Bp Chemicals Additives | Lubricating oil composition |
US5726133A (en) * | 1996-02-27 | 1998-03-10 | Exxon Research And Engineering Company | Low ash natural gas engine oil and additive system |
GB9611428D0 (en) * | 1996-05-31 | 1996-08-07 | Exxon Chemical Patents Inc | Overbased metal-containing detergents |
EP0963429B1 (en) * | 1997-11-28 | 2012-03-07 | Infineum USA L.P. | Lubricating oil compositions |
US5906969A (en) * | 1998-05-01 | 1999-05-25 | Exxon Research And Engineering Company | High fuel economy passenger car engine oil |
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