US20070167334A1 - Lubricating fluids - Google Patents
Lubricating fluids Download PDFInfo
- Publication number
- US20070167334A1 US20070167334A1 US11/333,689 US33368906A US2007167334A1 US 20070167334 A1 US20070167334 A1 US 20070167334A1 US 33368906 A US33368906 A US 33368906A US 2007167334 A1 US2007167334 A1 US 2007167334A1
- Authority
- US
- United States
- Prior art keywords
- grease
- lubricating fluid
- fully formulated
- formulated lubricating
- test
- 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.)
- Abandoned
Links
- 239000012530 fluid Substances 0.000 title claims abstract description 66
- 230000001050 lubricating effect Effects 0.000 title claims abstract description 54
- -1 phosphate amine salts Chemical class 0.000 claims abstract description 76
- 239000000654 additive Substances 0.000 claims abstract description 72
- 239000002253 acid Substances 0.000 claims abstract description 63
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 62
- 230000000996 additive effect Effects 0.000 claims abstract description 54
- 239000010452 phosphate Substances 0.000 claims abstract description 47
- 239000004519 grease Substances 0.000 claims abstract description 38
- 239000002199 base oil Substances 0.000 claims abstract description 25
- 230000006872 improvement Effects 0.000 claims abstract description 16
- 238000012360 testing method Methods 0.000 claims description 83
- 239000000314 lubricant Substances 0.000 claims description 48
- 239000003112 inhibitor Substances 0.000 claims description 35
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 33
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 33
- 239000003795 chemical substances by application Substances 0.000 claims description 31
- 239000002270 dispersing agent Substances 0.000 claims description 28
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 25
- 229910052717 sulfur Inorganic materials 0.000 claims description 25
- 230000007797 corrosion Effects 0.000 claims description 24
- 238000005260 corrosion Methods 0.000 claims description 24
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 23
- 239000011593 sulfur Substances 0.000 claims description 23
- 239000004615 ingredient Substances 0.000 claims description 21
- 239000007866 anti-wear additive Substances 0.000 claims description 19
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 11
- 229910052802 copper Inorganic materials 0.000 claims description 11
- 239000010949 copper Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 11
- 150000002148 esters Chemical class 0.000 claims description 10
- 239000003607 modifier Substances 0.000 claims description 10
- 229920001973 fluoroelastomer Polymers 0.000 claims description 9
- 229920000058 polyacrylate Polymers 0.000 claims description 9
- 239000003963 antioxidant agent Substances 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000002781 deodorant agent Substances 0.000 claims description 6
- 239000003599 detergent Substances 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 238000005555 metalworking Methods 0.000 claims description 4
- 230000009467 reduction Effects 0.000 claims description 4
- 238000012546 transfer Methods 0.000 claims description 3
- 150000002826 nitrites Chemical class 0.000 claims description 2
- 230000008569 process Effects 0.000 claims description 2
- 239000008186 active pharmaceutical agent Substances 0.000 claims 1
- 229920000768 polyamine Polymers 0.000 abstract description 10
- 239000003921 oil Substances 0.000 description 64
- 235000021317 phosphate Nutrition 0.000 description 53
- 239000000203 mixture Substances 0.000 description 52
- 150000001412 amines Chemical class 0.000 description 20
- 239000012208 gear oil Substances 0.000 description 19
- 229910052698 phosphorus Inorganic materials 0.000 description 15
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 13
- 239000011574 phosphorus Substances 0.000 description 13
- 230000001590 oxidative effect Effects 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 230000003647 oxidation Effects 0.000 description 11
- 238000007254 oxidation reaction Methods 0.000 description 11
- 239000012141 concentrate Substances 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 150000001336 alkenes Chemical class 0.000 description 7
- 239000002585 base Substances 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 230000002829 reductive effect Effects 0.000 description 7
- 239000010802 sludge Substances 0.000 description 7
- 239000002966 varnish Substances 0.000 description 7
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 6
- 229910052796 boron Inorganic materials 0.000 description 6
- 241000894007 species Species 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 230000005540 biological transmission Effects 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- 239000000806 elastomer Substances 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 230000009429 distress Effects 0.000 description 4
- 238000011065 in-situ storage Methods 0.000 description 4
- 239000010687 lubricating oil Substances 0.000 description 4
- 150000002825 nitriles Chemical class 0.000 description 4
- 229920013639 polyalphaolefin Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- 239000003981 vehicle Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000005069 Extreme pressure additive Substances 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 150000001638 boron Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000007795 chemical reaction product Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
- 235000011007 phosphoric acid Nutrition 0.000 description 3
- 150000003016 phosphoric acids Chemical class 0.000 description 3
- 150000003017 phosphorus Chemical class 0.000 description 3
- 239000005077 polysulfide Substances 0.000 description 3
- 229920001021 polysulfide Polymers 0.000 description 3
- 150000008117 polysulfides Polymers 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 238000004901 spalling Methods 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-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
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 230000003749 cleanliness Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 230000006735 deficit Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000010722 industrial gear oil Substances 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 150000005673 monoalkenes Chemical class 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- 125000005328 phosphinyl group Chemical class [PH2](=O)* 0.000 description 2
- 125000005499 phosphonyl group Chemical class 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 231100000241 scar Toxicity 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
- 150000003852 triazoles Chemical class 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- 150000004869 1,3,4-thiadiazoles Chemical class 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- NRENOZNSHMLGOF-UHFFFAOYSA-N 2-sulfanyltriazole Chemical compound SN1N=CC=N1 NRENOZNSHMLGOF-UHFFFAOYSA-N 0.000 description 1
- JATLSJIWVNJRMN-UHFFFAOYSA-N 4-dodecyl-2h-triazole Chemical compound CCCCCCCCCCCCC1=CNN=N1 JATLSJIWVNJRMN-UHFFFAOYSA-N 0.000 description 1
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 description 1
- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 description 1
- HPZLYWRSZQYGCA-UHFFFAOYSA-N 7-methyloctyl heptanoate Chemical compound CCCCCCC(=O)OCCCCCCC(C)C HPZLYWRSZQYGCA-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical class NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 229920002449 FKM Polymers 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000003973 alkyl amines Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 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
- 150000003939 benzylamines Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 229910052810 boron oxide Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 244000145845 chattering Species 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 125000001117 oleyl 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])=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])[H] 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- MOWNZPNSYMGTMD-UHFFFAOYSA-N oxidoboron Chemical class O=[B] MOWNZPNSYMGTMD-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000004313 potentiometry Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000010689 synthetic lubricating oil Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 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
- 150000003557 thiazoles Chemical class 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 150000003582 thiophosphoric acids Chemical class 0.000 description 1
Images
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
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/223—Five-membered rings containing nitrogen and carbon only
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/28—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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/043—Mannich bases
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/022—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of hydrocarbons, e.g. olefines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/024—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of esters, e.g. fats
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
- C10M2219/066—Thiocarbamic type compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/106—Thiadiazoles
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/047—Thioderivatives not containing metallic elements
-
- 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
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
-
- 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
- C10N2040/20—Metal working
-
- 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
- C10N2060/00—Chemical after-treatment of the constituents of the lubricating composition
- C10N2060/14—Chemical after-treatment of the constituents of the lubricating composition by boron or a compound containing boron
Definitions
- the invention relates to lubricating fluids having essentially no low molecular weight (C30 or less) primary, secondary, tertiary or cyclic aliphatic amine to serve as a rust inhibitor.
- Oxidative stability, seal compatibility, protection from wear, and overall durability are highly sought after features of gears oils for both automotive and industrial applications.
- Original equipment manufacturers (OEMs) as well as the consuming public are constantly demanding improvements such as extended drain intervals from suppliers of gear oils.
- Enhanced oxidative stability is highly desired in driveline fluids (e.g., automotive transmissions and differentials) as well as in gear boxes used for various industrial applications.
- driveline fluids e.g., automotive transmissions and differentials
- gear boxes used for various industrial applications.
- Lubricants are expected to be able to pass lengthy oxidation tests, e.g. the extended L-60-1 test (comprising a 200 hr test for axle oils and 300 hr test for transmission oils).
- the lubricant preferably should be able to provide adequate cleanliness as well as viscosity control to pass these tests.
- antioxidants to the lubricating oil, either phenolic or arylamine types.
- formulators can choose to use certain base stocks and/or additive combinations which are less prone to oxidation.
- Gear oils that are expected to survive for long drain intervals should be able to leave seals undamaged so that no leakage occurs during the lifetime of the gear box.
- Axle and transmission seal materials in the U.S. and Europe include fluoroelastomer, nitrile and polyacrylate. Static and dynamic seal testing in the U.S. and Europe are part of industry and OEM performance specifications for both industrial and automotive gear oil.
- gear oil One important feature of a gear oil is its ability to prevent surface distress, which if severe enough, can ultimately lead to catastrophic failure of the gears.
- Gear distress or wear can be in the form of pitting, spalling, ridging, rippling, etc. for automotive gears, especially those in the differential because of the loads.
- anti-wear additives To control wear, it is common to add anti-wear additives to reduce or prevent damage. These additives preferably should be able to function at temperatures from sub-zero to temperatures around 160° C., which could be reached if the vehicle is subjected to severe operating conditions.
- anti-wear additives should be able to function in the presence of other aggressive additives that perform key functions, e.g. extreme pressure additives, and they preferably should be able to continue to function for long operating periods.
- U.S. Pat. No. 6,046,144 describes synergistic antioxidant compositions comprising amine salts of alkyl phosphates, and ethylenediamine, ammonium or metal salts of alkylarylsulfonates.
- U.S. Pat. No. 5,942,470 teaches the use of combining at least one oil soluble sulfur-containing extreme pressure or antiwear agent with at least one oil soluble amine salt of a partial ester of an acid of phosphorus and with at least one oil soluble succinimide dispersant of a formula defined in the patent.
- a lengthy list of many suitable amine salts of the partially esterified phosphorus is included in the patent. Primary amines are preferred.
- U.S. Pat. No. 5,763,372 discusses “clean gear” boron-free gear additive systems, which employ an ashless boron-free dispersant, a sulfur source, and a phosphorus source, wherein at least one is chosen from a group of oil-soluble amine salts of acid phosphates.
- U.S. Pat. No. 5,756,429 describes a composition suitable for high speed gears having a peripheral speed of at least 10 m/sec containing a base oil having a % Ca of 5 or less and a S, P, N ratio of 100N/(S+P) between 4 and 10 by weight.
- Use of acid phosphates and their amine salts are preferred.
- the composition is said to be able to inhibit sludge and permit the prolongation of the life of an oil seal.
- U.S. Pat. No. 5,573,696 and U.S. Pat. No. 5,500,140 discuss the preparation of amine-neutralized acid phosphates, which are prepared by reacting P 2 O 5 with an alcohol prepared from the reaction of an epoxide with dihydrocarbyl phosphorothioic acid.
- U.S. Pat. No. 5,547,596 describes a lubricant composition for the limited slip differential (LSD) of a car which is obtained by adding a phosphate amine salt, such as an amine salt of an oleyl acid phosphate and a borated ashless dispersant, such that the ratio of N/P is 0.5-1.0; the ratio of N/B is 4-10; the phosphorus content is in the range of 0.15-0.4% by weight; and the boron content is in the range of 0.01 to 0.04% by weight.
- This lubricant composition inhibits the generation of chattering during the operation of a LSD device and has excellent oxidative stability.
- U.S. Pat. No. 5,354,484 describes how improved high temperature stability can be achieved with the presence of at least one soluble tertiary aliphatic primary amine salt, wherein the primary amine contains 4-30 carbon atoms, at least one of which is a substituted phosphoric acid, in combination with a borated succinimide dispersant.
- U.S. Pat. No. 5,328,619 describes an additive concentrate comprising at least one oil soluble organic acid, e.g. one or more hydrocarbyl phosphoric acids, one or more carboxylic acids or a combination of the two, and a hydrocarbyl amine which is added such that the pH of the finished concentrate is in the 6.0-7.0 range.
- a borated dispersant is introduced into the concentrate being formed when the concentrate is at least 6.0.
- the resulting compositions are said to inhibit haze in the resulting concentrates, and the pH control can provide gear compositions having enhanced extreme pressure performance in the L-42 test, and improved rust in the L-33 test.
- U.S. Pat. No. 4,575,431 discusses the combination of dihydrocarbyl hydrogen thiophosphates and hydrocarbyl dihydrogen phosphates and dihydrocarbyl hydrogen phosphates, with the phosphates being at least 50% neutralized with a hydrocarbyl amine that is C10-C30.
- U.S. Pat. No. 4,431,552 discusses a lubricating composition having dispersed therein a hydrated alkali metal borate extreme pressure agent and an effective amount of a mixture of a phosphate, a monothiophosphate, and a dithiophosphate. All of the phosphates are preferably used as their hydrocarbyl amine salts.
- U.S. Pat. No. 4,118,328 discusses the preparation and use of phosphate salts comprised of heating a triaryl phosphate and a primary or secondary aliphatic amine in a 1-20 molar ratio, respectively, with a trace amount of boric acid for catalyst.
- U.S. Pat. No. 3,728,260 describes the preparation of a neutral hydrocarbyl phosphate in combination with an alkyl amine hydrocarbyl phosphate salt for improved load carrying.
- EP 531 585 describes the use of an additive composition which includes a borated Mannich dispersant, a sulfur containing anti-wear or EP agent, a metal free phosphorus-containing antiwear-EP agent, and an oil-soluble amine salt of a carboxylic acid. Free amine may or may not be present, and may or may not be complexed to the phosphorus antiwear agent.
- EP 519 760 B1 teaches that an oil soluble amine is used to adjust the pH of an additive concentrate to 6-7 then dispersant is added after this adjustment is made.
- EP 391 653 B1 and EP 450 208 B1 both discuss having high concentrations of amines along with suitable quantities of weak acids, e.g. carboxylic acids, in the presence of sulfurized isobutylene and P-containing antiwear additives to provide gear oils with improved gear performance based on the results of a Planetary Spur Gear Test.
- weak acids e.g. carboxylic acids
- WO 03/1004620 A2 discusses a lubricating composition with improved efficiency for an emissions control system, wherein the compositions contain a metal-containing detergent, a metal salt of one or more phosphorus acids or the corresponding esters, and an acylated nitrogen-containing compound having at least 10 carbon atoms.
- the resulting TBN composition has a phosphorus concentration of up to about 0.12%.
- U.S. Pat. No. 4,900,460 covers sulfurized olefins reacted with phosphates and phosphites.
- the reaction product is useful as an extreme pressure and wear additive for lube compositions.
- U.S. Pat. No. 3,513,093 describes a composition containing a major part of a lubricating oil and minor portion of a substituted polyamine, which is prepared by reacting a polyamine with a succinic acid producing hydrocarbon having at least 50 carbons with at least 0.001 moles of a phosphorus acid producing compound selected from the class of phosphoric acids, phosphorus acids, phosphonyl acids, phosphinyl acids, etc. These species were found to give improved oxidation performance in a variety of bench and engine tests.
- U.S. Pat. No. 2,224,695 teaches the preparation of a corrosion inhibitor for metals which comprises an ester of an acid of phosphorus having at least one of the hydrogen atoms of the acid replaced by an ester group and at least one of the hydrogen atoms replaced by an inorganic radical, upon exposing it to a metal surface. Under favorable conditions, it reacts chemically with metal surfaces to form a protective coating and inhibit corrosive wear.
- EP 531 000 B1 discusses an additive composition containing a.) a reaction product of a phosphorus or thiophosphorus acid with an ashless dispersant and a boron compound and b.) a sulfur containing antiwear-EP agent.
- the gear oil prepared with these components is said to have these performance improvements: 1.) inhibition of scoring/scuffing, 2.) improved wear in the form of ridging, rippling, pitting and spalling, 3.) improved oxidation in the form of reduced sludge and varnish deposits, especially at higher temperatures.
- a lubricant or grease composition which does not include primary, secondary, tertiary, cyclic aliphatic low molecular weight ( ⁇ C30) monoamines or polyamines and/or the corresponding acid phosphate amine salts which, in preferred embodiments, exhibits improved performance in at least one of oxidative stability, seal compatibility, and anti-wear protection, while causing no significant deficits in other important areas of performance.
- the invention is directed to a lubricating fluid or grease, the improvement comprising the absence of primary, secondary, tertiary, and cyclic hydrocarbyl amines with a carbon number of less than C30 and the absence of the corresponding acid phosphate amine salts.
- the additive system used in the lubricating fluid is characterized by possessing a total base number (TBN) of less than 22.
- the invention is further characterized as comprising an effective amount of an acid phosphate antiwear additive.
- the phosphate antiwear additive will be at least one mono- and/or dialkyl acid phosphate effective for antiwear protection.
- Preferred mono- and/or dialkyl acid phosphates are represented by the formula (R 1 O)(R 2 O)P(O)OH, where R 1 is hydrocarbyl and R 2 is hydrocarbyl or hydrogen. R 1 and R 2 may have the same or different hydrocarbyl groups.
- the present invention is also directed to the use of such lubricating fluids and greases in gears, drives, axles, transmissions, and the like, in hydraulic and circulating systems, and in metal working.
- the invention is further directed to the use of apparatus comprising seals and lubricating fluids and/or greases in contact with said seals, the improvement comprising fluids and/or grease including the additive package in accordance with embodiments of the invention.
- FIG. 1 is a comparison of TBN for additive systems according to embodiments of the invention versus a commercial additive package.
- FIG. 2 is a comparison of the carbon varnish rating of formulations according to embodiments of the present invention versus comparative formulations.
- a lubricating fluid or grease is provided without the use of primary, secondary, tertiary, or cyclic hydrocarbyl amine rust inhibitors with a carbon number of C30 or less, or the corresponding acid phosphate amine salts which, in certain embodiments, provides improvements in at least one of the areas of oxidation stability, seal compatibility and anti-wear performance, while causing no appreciable deficits in other areas of performance. More particularly, the invention relates to lubricating compositions useful in automotive gear boxes and differentials as well as industrial gear boxes.
- fully formulated lubricating oils/greases and functional fluid compositions comprise an acid phosphate antiwear additive, preferably one or more hydrocarbyl or dihydrocarbyl acid phosphates, and there are essentially no acid phosphate hydrocarbyl amine salts, where the hydrocarbyl mono or polyamine is C30 or less, present in said fully formulated compositions.
- an acid phosphate antiwear additive preferably one or more hydrocarbyl or dihydrocarbyl acid phosphates, and there are essentially no acid phosphate hydrocarbyl amine salts, where the hydrocarbyl mono or polyamine is C30 or less, present in said fully formulated compositions.
- the term “phosphate” does not include any of the sulfur-containing compounds, e.g., thiophosphate compounds.
- the acid phosphate may be present as the mono and/or dihydrocarbyl esters of the acid phosphate.
- the resulting gear lubricant is essentially free of hydrocarbyl primary, secondary, tertiary, and cyclic amine rust inhibitors with 30 carbons or less as an ingredient (when the invention is expressed as a “recipe” of ingredients) and therefore the final fully formulated lubricant is essentially free of the corresponding acid phosphate amine salts.
- “essentially free of” allows for minor amounts, such as inevitable impurities which might lead to the presence of one or more of primary, secondary, tertiary, or cyclic aliphatic low molecular weight amines with 30 carbons (C30) or less and/or the presence of the corresponding acid phosphate amine salts but these ingredients and the constituents that form them are not present in an amount that might effect the novel and basic characteristics of the lubricating fluid.
- the additive system will have a significantly reduced total base number (TBN) for the package.
- TBN total base number
- the additive concentrates covered by this invention have a TBN ⁇ 22, some cases less than 20, or less than 15, or less than 10, or even less than 5.
- FIG. 1 is a plot of TBN and TAN (Total Acid Number) of a commercial additive package versus additive packages according to embodiments of the present invention.
- the commercial additive package was chosen because it has the lowest TBN in the population of commercial additive packages examined by the inventors. All other commercial packages tested by the inventors had higher TBN numbers. It is highly surprising that the additive packages according to embodiments of the present invention can provide the benefits set forth herein with low TBN in view of the TBN of prior art commercial products.
- the first of these performance benefits is enhanced antiwear performance.
- testing according to the industry-recognized L-37 rig test (ASTM D6121) has shown significant improvements particularly in the low temperature version (conventionally known as the “Canadian version”) of this test.
- the oxidative stability of gear oils without the hydrocarbyl amine rust inhibitor described earlier is superior to those with such an amine present. It has been shown that when the low molecular ( ⁇ C30) hydrocarbyl amines are eliminated from a gear lubricant, the oxidation performance is dramatically improved. This can be demonstrated using the industry oxidation test called the L-60-1 (ASTM D5704).
- the finished gear lubricant according to embodiments of the present invention also include at least one of the ingredients from the group consisting of: a sulfur-containing extreme pressure (EP) agent, a nitrogen-containing dispersant, and a corrosion inhibitor.
- Other preferred additives may include at least one ingredient selected from the group consisting of: borated dispersants, non-aminic rust inhibitors, defoamants, pour point depressants, antioxidants, demulsifiers, friction modifiers, seal swell agents, chromophores, deodorants, limited slip additives, detergents, and tackifiers.
- the invention is directed to a lubricant comprising a major amount of an oil of lubricating viscosity and a minor amount of at least one substituted phosphoric acid composition characterized by the formula (R 1 O)(R 2 O)P(O)OH, where R 1 is a hydrocarbyl group and R 2 is either hydrogen or a hydrocarbyl group.
- major amount means present in an amount greater than any other ingredient, based on wt. %.
- the “oil of lubricating viscosity” will also be described as a “base oil” herein, and may be a combination of one or more base oils, with the term “major amount” meaning the sum of the base oils are present in an amount greater than any other ingredient.
- the lubricant composition preferably will also contain a sulfur-containing extreme pressure agent.
- the lubricant composition preferably also will contain nitrogen-containing dispersants and corrosion inhibitors, with the proviso that said species not include low molecular weight primary, secondary, tertiary, or cyclic aliphatic mono and/or polyamines with 30 carbons or less.
- the products according to embodiments of the invention may be used for a wide variety of automotive and industrial gear applications. Examples of such applications include use in hypoid axles and in mechanical steering drives in passenger cars and in cross-country vehicles.
- the products based on embodiments of the present invention may be used in planetary hub reduction axles, mechanical steering and transfer gear boxes in utility vehicles such as trucks. It also can be used in different types of gear boxes, e.g. synchromesh gear boxes, as well as power take-off gears, limited slip axles, and Planetary hub reduction gear boxes.
- the lubricating oil and functional fluid compositions according to embodiments of the present invention are based on diverse oils of lubricating viscosity, including natural and synthetic lubricating oils and mixtures thereof. These lubricating compositions are particularly effective as gear lubricants for both industrial and automotive gear applications, but could also be considered for other lubricant applications, e.g. hydraulic, metal working, turbine, circulating, and small engine.
- compositions according to embodiments of the invention may further comprise one or more base oils. It will be recognized that in certain instances it may be convenient to have a lubricant composition which is not completely formulated, i.e., with a minor amount of additives left to be added by the final end consumer, for the purposes of the present disclosure a “fully formulated” lubricant composition means that any additional components to be added do not affect the novel and basic characteristics of the lubricant according to the present invention.
- Fluids that can meet the criteria of base oil for lubricant and functional fluids are varied. They may fall in any of the well-known American Petroleum Institute (API) categories of Group I through Group V.
- the API defines Group I stocks as solvent-refined mineral oils. Group I stocks contain the most unsaturates and sulfur and have the lowest viscosity indices. Group I defines the bottom tier of performance. Group II and III stocks are high viscosity index and very high viscosity index base stocks, respectively.
- the Group III oils contain the lowest level of unsaturates and sulfur relative to Group I and II oils. With regard to certain characteristics, both Group II and Group III oils perform better than Group I, particularly in the area of oxidative stability and low temperature performance.
- Group IV stocks consist of polyalphaolefins, which can be produced via the catalytic oligomerization of linear alphaolefins (LAOs), with particularly preferable LAOs selected from C 5 -C 14 linear alphaolefins, more preferably from 1-hexene to 1-tetradecene, more preferably from 1-octene to 1-dodecene, and mixtures thereof, although oligomers of lower olefins such as ethylene and propylene, oligomers of ethylene/butene-1 and isobutylene/butene-1, oligomers of ethylene with other higher olefins, such as described in U.S. Pat. No. 4,956,122, and the patents referred to therein, and the like, may also be used.
- PAOs typically offer superior volatility, thermal stability, and pour point characteristics to those base oils in Group I, II, and III.
- Group V includes all the other base stocks not included in Groups I through IV.
- Group V base stocks include, e.g., esters, alkylated aromatics, polyinternal olefins (PIOs), polyisobutylenes, polyalkylene glycols (PAGs), etc.
- One of the benefits of embodiments of the present invention is that it may be applicable to base oils fitting into any of the above five categories, API Groups I to V, as well as other materials.
- the lubricating compositions of the invention comprise an additive system which includes ingredients selected from the group consisting of: one or more sulfur-containing extreme pressure agents, one or more acid phosphates (pentavalent phosphorus), one or more ashless dispersants, one or more corrosion inhibitors, and optionally anti-foamants, pour point depressants, friction modifiers, demulsifiers, tackifiers, VI improvers, deodorants, seal swell agents, and non-amine rust inhibitors, and mixtures thereof, with the proviso that it is essentially free of: (a) low molecular weight (C30 or less) primary, secondary, tertiary, and cyclic hydrocarbyl amines; and (b) the corresponding acid phosphate amine salts.
- an additive system which includes ingredients selected from the group consisting of: one or more sulfur-containing extreme pressure agents, one or more acid phosphates (pentavalent phosphorus), one or more ashless dispersants, one or more corrosion inhibitors
- Extreme pressure (EP) agents used in the composition according to embodiments of the invention include sulfur-containing and boron-containing EP agents. Sulfur-containing EP agents are preferred.
- Sulfurized olefins may be useful in providing protection against high pressure, metal-to-metal contacts in industrial and automotive gear oils.
- sulfur-containing extreme pressure additive that can be used in the additive package.
- Sulfur-containing components useful in this regard included sulfurized olefins, dialkyl polysulfides, diarylpolysulfides, sulfurized fats and oils, sulfurized fatty acid esters, trithiones, sulfurized oligomers of C2-C8 monoolefins, thiophosphoric acid compounds, sulfurized terpenes, thiocarbamate compounds, thiocarbonate compounds, sulfoxides, and thiol sulfinates.
- Mixtures of sulfur-containing EP components may be used.
- the preferred sulfur-containing EP components are selected from sulfurized oligomers of C2-C8 monoolefins, olefins sulfides, and dialkyl and diaryl polysulfides.
- the more preferred extreme pressure agents are oligomeric olefin sulfides and dialkyl polysulfides.
- the sulfurized olefin is prepared via a high pressure sulfurization procedure.
- boron-containing EP additives may be adequate, provided that significant amounts of water are not present to cause hydrolysis.
- Use of boron-containing EP agents alone or with sulfur-containing EP agents are both contemplated.
- the composition does not use an extreme pressure ingredient containing boron.
- Dispersants serve inter alia to keep sludge and varnish particles from coating on the gear surfaces. There are no particular restrictions on the type used, though it is preferable that at least one contains nitrogen. Nitrogen-containing dispersants include alkyl succinimides, alkenyl succinimides, benzylamine compounds (Mannich bases), polybutenylamines, and the like. Borated versions of any of these are optional.
- nitrogen-containing dispersants are selected from alkyl succinimides and alkenyl succinimides.
- the especially preferred ashless dispersant for use in this invention are the products of reaction of a polyethylene polyamine, e.g. tetraethylene pentamine, with a hydrocarbon-substituted anhydride made by the reaction of a polyolefin, preferably having a molecular weight of about 700-5000 and especially 800-3000 (it is not particularly important whether this is number average molecular weight or weight average molecular weight) with an unsaturated polycarboxylic acid or anhydride, e.g. maleic anhydride.
- Corrosion inhibitors or metal passivators are typically additives that are heterocyclic in nature and are nitrogen-, and optionally, sulfur-containing.
- Triazole and its derivatives have been found to prevent corrosion in gear oils. Some specific examples include benzotriazole, tolyltriazole, 2-mercaptotriazole, dodecyltriazole. Alkyl and aryl derivatives are preferred.
- a specific class of passivators is known as “copper passivators.” These comprise a class of compounds which includes thiadiazoles, triazoles, and thiazoles. The preferred compounds are the 1,3,4-thiadiazoles.
- an effective amount of at least one mono- and/or dialkyl acid phosphate for antiwear protection Preferred mono- and/or dialkyl acid phosphates antiwear additives include at least one species represented by the formula (R 1 O)(R 2 O)P(O)OH, where R 1 is hydrocarbyl and R 2 is hydrocarbyl or hydrogen. R 1 and R 2 may have the same or different hydrocarbyl groups. Suitable hydrocarbyl groups have 1-40 carbon atoms, preferably 2-20 and more preferably 3-20.
- the preferred acid phosphates are selected from mono- and di-2-ethylhexyl acid phosphates and mixtures thereof.
- Acid phosphates would be preformed salts comprising the acid phosphate and a low molecular weight hydrocarbyl amine or the acid phosphate salt would be formed in situ in the additive package or the finished lubricant or grease (or at some other point between prior to or even during actual use).
- Such salts are described in, e.g., U.S. Pat. Nos. 2,063,629, 2,224,695, 2,447,288, 2,616,905, 3,728,260, 3,984,448, and 4,431,552.
- the hydrocarbyl amine is often termed a “rust inhibitor” and is usually a low molecular weight (, less than or equal to C30, i.e., ⁇ C30) primary or secondary, mono or polyamine, but could also be tertiary or cyclic mono/polyamines.
- the preferred amines are generally aliphatic in nature and possess from 4-30 carbon atoms. Some specific examples include the following: octylamine, decenylamine, dodecenylamine, oleylamine, and the like.
- the most preferred amines are described as a complex with acid phosphates, where the aliphatic group of the amine is a tertiary alkyl group and the amine is a primary amine.
- Primene 81-R and Primene JMT amines are typically describes as most preferred.
- Optional additives that may be included in the additive concentrate or the lubricating composition include: defoamants, non-aminic rust inhibitors, seal swell agents, friction modifiers, antioxidants, deodorants, chromophores, pour point depressants, tackifiers, demulsifiers, detergents, VI modifiers, and mixtures thereof.
- defoamants non-aminic rust inhibitors, seal swell agents, friction modifiers, antioxidants, deodorants, chromophores, pour point depressants, tackifiers, demulsifiers, detergents, VI modifiers, and mixtures thereof.
- ingredients may combine with the other ingredients to form salts, adducts, coordinated species, and the like.
- the combination of such species may be formed prior to addition to the final lubricant fluid (e.g., in an additive package), they may be formed in situ with a small amount of diluent (typically the final basestock) or they may be formed in situ after the ingredients are added to the basestock.
- diluent typically the final basestock
- Various combinations are possible. With this in mind, the present disclosure thus should be read in the nature of a recipe as regards the various additive described herein.
- additive package should be taken to mean any one additive package used or the entire sum of ingredients added to the one or more base oils used to create the final fully formulated composition.
- the oils were tested in the rig tests that are incorporated into API and SAE standards GL-5 and J2360, respectively.
- the L-37 test was used to assess antiwear performance; the L-60-1 was used for oxidative and thermal stability; and the static seal test ASTM D5662 was run for polyacrylate and fluoroelastomer seal compatibility.
- the L-42 for protection against scoring and the L-33 and ASTM D130 for corrosion protection were also run to demonstrate no deficiencies as a result of amine elimination.
- ASTM D2783 Four Ball EP test and ASTM D665 for rust were run.
- the test apparatus is a new, complete hypoid truck axle assembly, Dana Model 60 with 5.86 to 1 ratio.
- the assembly is mounted on a test stand with the pinion and axle shafts' center lines horizontal.
- the gears are first run through a conditioning phase and then through a test phase.
- the test phase is 24 h+0.2 h and is run at 275° F. with a load of 1740 ft-lb on each wheel and 80 rpms/min.
- the differential is disassembled and the ring gear and pinion are inspected and rated for each type of distress (e.g. spalling, pitting, ridging, wear, rippling, etc.). The rating value is reported.
- the oxidative and thermal stability were evaluated in ASTM D5704 or the L-60/L-60-1 test, which is the most common test procedure for evaluating these features of automotive gear oils.
- the test covers the oil-thickening and insolubles/deposit formation characteristics of the lubricant when subjected to high temperature oxidizing conditions.
- the candidate lubricant is heated to 325° F./163° C. for 50 hr in a small gear box with two lightly loaded spur gears. Air is bubbled through the oil at a rate of 1 L/hr.
- the viscosity of the oxidized oil is measured at the end of the test and compared to the initial value.
- the pentane and toluene insolubles are also measured.
- the L-60-1 test is run in the same manner; however, the carbon-varnish and sludge are measured along with the insolubles and the viscosity increase.
- ASTM D5662 was run. This is a laboratory test method which evaluates gear oils for compatibility with various elastomers: nitrile, polyacrylate, and fluoroelastomer. This method addresses failures that may be caused by excessive elastomer hardening, elongation loss, and volume swell and attempts to determine the likelihood that an oil might cause premature sealing system failures in the field. Specimens are cut from the elastomer being evaluated and are immersed in oil for 240 hr. Reference oils are run periodically. The test temperature is dependent on the type of seal material used: 100° C. for nitrile and 150° C. for fluoroelastomer and polyacrylate. At the end of 240 hr, the aged elastomer specimens are tested for changes in hardness, elongation, tensile strength and volume.
- Lubricating compositions, Oils A 1 and A 2 were prepared in accordance with embodiments of the invention whereas Oils X 1 and X 2 were formulated for comparison.
- the contents of these fluids are shown in Table 1 below.
- the additive systems of all examples use identical components, differing only in percentages.
- the additive percentages of X 1 and X 2 were manipulated to provide the closest approach to the percent of S, P, and N additives in A 1 and A 2 , respectively, which is believed to provide the most valid comparison.
- the key difference between A 1 and X 1 , and between A 2 and X 2 is the omission of the hydrocarbyl primary amine rust inhibitor in examples A 1 and A 2 .
- Oils A 1 and A 2 had much improved carbon-varnish ratings compared with Oil X 1 and Oil X 2 .
- the results are shown in Table 2. Based on this test alone, the ratings results for Oils X 1 and X 2 are considered as “failing”.
- FIG. 2 shows graphically the superior C-V performance of the candidate oils. Since the cleanliness is related to the C-V rating, it can be stated that the oils are cleaner. Pentane and toluene insolubles were non-existent for Oils A 1 and A 2 but around 0.3-0.4 mass percent for the oils X 1 and X 2 . The sludge rating for all four oils was not significantly different.
- oils were evaluated in the ASTM D130 Copper Corrosion Test as well as in the L-33 Rust Test.
- the copper strip was rated 1b for all four oils. It is somewhat surprising that formulations without the aminic rust inhibitor achieves the same result as the commercially acceptable formulations with the rust inhibitor. In the L-33 test, all formulations were well above the pass/fail line of 9.0 as referenced in SAE J2360 (see Table 2 for data).
- a steel ball is rotated atop of three clamped balls at a rate of 1800 rpms for 60 minutes under a force of 20 kg at 75° C. The average wear scar of the three clamped balls is then determined.
- ASTM D665 is used to measure protection from steel corrosion.
- a mixture of test oil is mixed with either distilled water (Part A) or synthetic sea water (Part B) at a temperature of 60° C. with a cylindrical steel rod completely immersed. After four hours, the test rod is examined for signs of rusting. Copper corrosion performance was roughly equivalent for the two oils as determined by ASTM D130.
- the results for Oil B and comparison Oil Y are shown in Table 4.
- Preferred embodiments include a fully formulated lubricating fluid or grease including an effective amount of an acid phosphate-containing antiwear additive, characterized as comprising an additive package and a major amount of at least one base oil, the improvement comprising the absence of low molecular weight primary, secondary, tertiary, and cyclic aliphatic amines of 30 carbons or less and the absence of the corresponding acid phosphate amine salts, with still more preferred embodiments, which may be combined as would be recognized by one of ordinary skill in the art in possession of the present disclosure, selected from: (i) wherein said additive package has a TBN ⁇ 22 (or TBN ⁇ 20, or TBN ⁇ 15, or TBN ⁇ 10, or TBN ⁇ 5; (ii) wherein said acid phosphate is selected from at least one mono and/or dihydrocarbyl ester of an acid phosphate characterized by the formula (1): (R 1 O)(R 2 O)P(O)OH, where R 1 is a hydrocarbyl group and R 2 is
- Another preferred embodiment is an apparatus comprising at least one seal and a lubricating fluid or grease in contact with said seal, wherein said lubricating fluid or grease is that characterized in the previous paragraph, particularly an apparatus wherein the seal comprises at least one material selected from fluoroelastomers, nitrites, and polyacrylates, and also particularly wherein the apparatus, which may have the seal as just described, comprises at least one of the following: a hypoid axle, a mechanical steering drive or gear box, a planetary hub reduction axle or gear box, a transfer gear box, a synchromesh gear box, a power take-off gear, a limited slip axle, an engine or turbine, a hydraulic system.
- Still other particularly preferred embodiments are: a process for metal working or in a circulating fluid system, either comprising the use of a lubricant or grease, the improvement comprising the use of the lubricating fluid or grease as described in the paragraph just above the immediately preceding paragraph.
- Yet still another particularly preferred embodiment is a fully formulated lubricating fluid or grease suitable for use in driveline fluids and/or gear boxes for industrial applications comprising an additive package and a major amount of at least one base oil and essentially free of low molecular weight primary, secondary, tertiary, and cyclic aliphatic amines of 30 carbons or less and their corresponding acid phosphate salts, which may be modified in numerous ways described herein, particularly in any of the ways described in paragraph [00112], but in the important embodiment which may be characterized as containing an acid phosphate selected from at least one mono and/or dihydrocarbyl ester of an acid phosphate characterized by the formula (1): (R 1 O)(R 2 O)P(O)OH, where R 1 is a hydrocarbyl group and R 2 is selected from hydrogen or a hydrocarbyl group, especially wherein at least one of R 1 and R 2 is 2-ethylhexyl.
- a particularly preferred embodiment also is a method for lubricating an apparatus, the method comprising applying a lubricant to the apparatus wherein said lubricant comprises a base oil, an effective amount of an acid phosphate-containing antiwear additive, said lubricant further characterized as essentially free of primary, secondary, tertiary and cyclic hydrocarbyl amines with a carbon number of C30 or less and the corresponding salts of said acid phosphate, which may of course be modified by any one or more of the limitations set forth in paragraph [00112].
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Description
- The invention relates to lubricating fluids having essentially no low molecular weight (C30 or less) primary, secondary, tertiary or cyclic aliphatic amine to serve as a rust inhibitor.
- Oxidative stability, seal compatibility, protection from wear, and overall durability are highly sought after features of gears oils for both automotive and industrial applications. Original equipment manufacturers (OEMs) as well as the consuming public are constantly demanding improvements such as extended drain intervals from suppliers of gear oils.
- Enhanced oxidative stability is highly desired in driveline fluids (e.g., automotive transmissions and differentials) as well as in gear boxes used for various industrial applications. When oxidation is problematic, sludge and carbon/varnish deposits appear on the gear surfaces, which may adversely impact the functioning of the gears. Lubricants are expected to be able to pass lengthy oxidation tests, e.g. the extended L-60-1 test (comprising a 200 hr test for axle oils and 300 hr test for transmission oils). The lubricant preferably should be able to provide adequate cleanliness as well as viscosity control to pass these tests.
- In order to prepare lubricants which are oxidatively stable, it has become common practice to add antioxidants to the lubricating oil, either phenolic or arylamine types. Alternatively, formulators can choose to use certain base stocks and/or additive combinations which are less prone to oxidation.
- Gear oils that are expected to survive for long drain intervals should be able to leave seals undamaged so that no leakage occurs during the lifetime of the gear box. Axle and transmission seal materials in the U.S. and Europe include fluoroelastomer, nitrile and polyacrylate. Static and dynamic seal testing in the U.S. and Europe are part of industry and OEM performance specifications for both industrial and automotive gear oil.
- One important feature of a gear oil is its ability to prevent surface distress, which if severe enough, can ultimately lead to catastrophic failure of the gears. Gear distress or wear can be in the form of pitting, spalling, ridging, rippling, etc. for automotive gears, especially those in the differential because of the loads. To control wear, it is common to add anti-wear additives to reduce or prevent damage. These additives preferably should be able to function at temperatures from sub-zero to temperatures around 160° C., which could be reached if the vehicle is subjected to severe operating conditions. In addition, to perform most effectively, anti-wear additives should be able to function in the presence of other aggressive additives that perform key functions, e.g. extreme pressure additives, and they preferably should be able to continue to function for long operating periods.
- There are industry tests for examining the effectiveness of antiwear additive systems. In the automotive industry, the L-37 is most widely recognized. This rig test simulates low speed, high torque operation. A low temperature modification of this test is also part of the API GL-5 and SAE J2360 specification for 75W graded gear lubricants. The low temperature version of this test is known as the Canadian version. There also exists a high temperature version of the L-37 test, which is included in several OEM specifications. In the L-37 test, and its variants, the gears are disassembled at the end of the test and the gear distress is rated.
- Commonly used anti-wear additives are phosphorous containing compounds. They usually include amine-neutralized salts of phosphorus acids, phosphinyl acids, phosphonyl acids, thiophosphorus acids, thiophosphinyl acids, thiophosphonyl acids, and the partial esters of these. The amines useful in preparing the amine salts are primary or secondary hydrocarbyl monoamines or polyamines containing about 4-30 carbon atoms. They may also be tertiary or cyclic amines. The most common amines are primary, fatty amines containing 10-20 carbon atoms, like octadecyl amine or tertiary alkyl amines like C12-C14 tertiary alkyl primary amine, commercially available as “Primene 81-R.” It is commonly believed that the amine neutralization is a necessary feature of the different phosphorus-containing compounds, because of its ability to impart critically required steel corrosion protection and thermal stability.
- In order to reach the extended drain intervals that OEMs are now seeking for their gear boxes and differentials, durability is important for gear oils, both automotive and industrial. The durability of a fluid will depend on the base oils that are being used, e.g. synthetic base oils will be far more durable than API Group I and II fluids because of the superior oxidative and thermal stability. However, base oil selection is only part of the picture for formulating gear oils with improved durability. The additive system must also be carefully chosen so as to provide oxidation stability, seal compatibility and antiwear performance, all of which contribute to an oil's durability.
- Industrial and automotive gear lubes perform in much the same way, though loads on the industrial gears tend to be spread out over larger surface areas and therefore are not as great as those seen in the rear axle of an automotive vehicle. Nevertheless, similar features would be considered desirable in both types of gear oils. Durability, for example, is important as this would equate to longer drain intervals and reduced down time and reduced maintenance costs. Durability in the form of improved oxidative stability, reduced wear and better seal compatibility are highly desired for all types of gear oils.
- Because there are numerous additives added to such compositions for many diverse reasons and with each additive interacting with all the other additives in some manner, it is extremely difficult to find new formulations showing an improvement in at least one property while having little or no detrimental effects on other properties.
- U.S. Pat. No. 6,844,300 and EP 1 233 051 A1 teach that a gear oil comprising a base oil, a thermally stable P-containing antiwear additive and a metal free sulfur EP agent, wherein the S is present at least at a level of 10,000 ppms, and the P is present from 100-350 ppms will meet GL-5 requirements. The thermally stable antiwear additive is defined as oil soluble amine salts of phosphoric acid esters as well as reaction products of dicyclopentadiene and thiophosphoric acid. The salts may be formed beforehand or in situ.
- U.S. Pat. No. 6,046,144 describes synergistic antioxidant compositions comprising amine salts of alkyl phosphates, and ethylenediamine, ammonium or metal salts of alkylarylsulfonates.
- U.S. Pat. No. 5,942,470 teaches the use of combining at least one oil soluble sulfur-containing extreme pressure or antiwear agent with at least one oil soluble amine salt of a partial ester of an acid of phosphorus and with at least one oil soluble succinimide dispersant of a formula defined in the patent. A lengthy list of many suitable amine salts of the partially esterified phosphorus is included in the patent. Primary amines are preferred.
- U.S. Pat. No. 5,763,372 discusses “clean gear” boron-free gear additive systems, which employ an ashless boron-free dispersant, a sulfur source, and a phosphorus source, wherein at least one is chosen from a group of oil-soluble amine salts of acid phosphates.
- U.S. Pat. No. 5,756,429 describes a composition suitable for high speed gears having a peripheral speed of at least 10 m/sec containing a base oil having a % Ca of 5 or less and a S, P, N ratio of 100N/(S+P) between 4 and 10 by weight. Use of acid phosphates and their amine salts are preferred. The composition is said to be able to inhibit sludge and permit the prolongation of the life of an oil seal.
- U.S. Pat. No. 5,691,283 describes a transmission and axle or differential gearing which comprises a base oil and a Mannich dispersant, a sulfur-containing EP agent, a P- and N-containing antiwear additive, and an overbased alkali or alkaline earth carboxylate, sulphonate, or sulfurized phenate having a TBN (Total Base Number) of at least 145.
- U.S. Pat. No. 5,573,696 and U.S. Pat. No. 5,500,140 discuss the preparation of amine-neutralized acid phosphates, which are prepared by reacting P2O5 with an alcohol prepared from the reaction of an epoxide with dihydrocarbyl phosphorothioic acid.
- U.S. Pat. No. 5,547,596 describes a lubricant composition for the limited slip differential (LSD) of a car which is obtained by adding a phosphate amine salt, such as an amine salt of an oleyl acid phosphate and a borated ashless dispersant, such that the ratio of N/P is 0.5-1.0; the ratio of N/B is 4-10; the phosphorus content is in the range of 0.15-0.4% by weight; and the boron content is in the range of 0.01 to 0.04% by weight. This lubricant composition inhibits the generation of chattering during the operation of a LSD device and has excellent oxidative stability.
- U.S. Pat. No. 5,358,650, U.S. Pat. No. 5,571,445, and WO 94/22990 describe a synthetic fluid which includes a variety of synthetic base oils plus specified amounts of the following: a sulfur-containing extreme pressure-antiwear agent, a P-containing antiwear agent, a corrosion inhibitor, an amine and/or carboxylic acid rust inhibitor, a foam inhibitor, and an ashless dispersant.
- U.S. Pat. No. 5,354,484 describes how improved high temperature stability can be achieved with the presence of at least one soluble tertiary aliphatic primary amine salt, wherein the primary amine contains 4-30 carbon atoms, at least one of which is a substituted phosphoric acid, in combination with a borated succinimide dispersant.
- U.S. Pat. No. 5,328,619 describes an additive concentrate comprising at least one oil soluble organic acid, e.g. one or more hydrocarbyl phosphoric acids, one or more carboxylic acids or a combination of the two, and a hydrocarbyl amine which is added such that the pH of the finished concentrate is in the 6.0-7.0 range. A borated dispersant is introduced into the concentrate being formed when the concentrate is at least 6.0. The resulting compositions are said to inhibit haze in the resulting concentrates, and the pH control can provide gear compositions having enhanced extreme pressure performance in the L-42 test, and improved rust in the L-33 test.
- U.S. Pat. No. 4,575,431 discusses the combination of dihydrocarbyl hydrogen thiophosphates and hydrocarbyl dihydrogen phosphates and dihydrocarbyl hydrogen phosphates, with the phosphates being at least 50% neutralized with a hydrocarbyl amine that is C10-C30.
- U.S. Pat. No. 4,431,552 discusses a lubricating composition having dispersed therein a hydrated alkali metal borate extreme pressure agent and an effective amount of a mixture of a phosphate, a monothiophosphate, and a dithiophosphate. All of the phosphates are preferably used as their hydrocarbyl amine salts.
- U.S. Pat. No. 4,118,328 discusses the preparation and use of phosphate salts comprised of heating a triaryl phosphate and a primary or secondary aliphatic amine in a 1-20 molar ratio, respectively, with a trace amount of boric acid for catalyst.
- U.S. Pat. No. 3,728,260 describes the preparation of a neutral hydrocarbyl phosphate in combination with an alkyl amine hydrocarbyl phosphate salt for improved load carrying.
- EP 531 585 describes the use of an additive composition which includes a borated Mannich dispersant, a sulfur containing anti-wear or EP agent, a metal free phosphorus-containing antiwear-EP agent, and an oil-soluble amine salt of a carboxylic acid. Free amine may or may not be present, and may or may not be complexed to the phosphorus antiwear agent.
- EP 519 760 B1 teaches that an oil soluble amine is used to adjust the pH of an additive concentrate to 6-7 then dispersant is added after this adjustment is made.
- EP 391 653 B1 and EP 450 208 B1 both discuss having high concentrations of amines along with suitable quantities of weak acids, e.g. carboxylic acids, in the presence of sulfurized isobutylene and P-containing antiwear additives to provide gear oils with improved gear performance based on the results of a Planetary Spur Gear Test.
- UK 2,108,147 examines the use of oil soluble overbased sodium salts of phosphate esters in lubricant compositions.
- WO 03/1004620 A2 discusses a lubricating composition with improved efficiency for an emissions control system, wherein the compositions contain a metal-containing detergent, a metal salt of one or more phosphorus acids or the corresponding esters, and an acylated nitrogen-containing compound having at least 10 carbon atoms. The resulting TBN composition has a phosphorus concentration of up to about 0.12%.
- U.S. Pat. No. 4,900,460 covers sulfurized olefins reacted with phosphates and phosphites. The reaction product is useful as an extreme pressure and wear additive for lube compositions.
- U.S. Pat. No. 3,513,093 describes a composition containing a major part of a lubricating oil and minor portion of a substituted polyamine, which is prepared by reacting a polyamine with a succinic acid producing hydrocarbon having at least 50 carbons with at least 0.001 moles of a phosphorus acid producing compound selected from the class of phosphoric acids, phosphorus acids, phosphonyl acids, phosphinyl acids, etc. These species were found to give improved oxidation performance in a variety of bench and engine tests.
- U.S. Pat. No. 2,224,695 teaches the preparation of a corrosion inhibitor for metals which comprises an ester of an acid of phosphorus having at least one of the hydrogen atoms of the acid replaced by an ester group and at least one of the hydrogen atoms replaced by an inorganic radical, upon exposing it to a metal surface. Under favorable conditions, it reacts chemically with metal surfaces to form a protective coating and inhibit corrosive wear.
- EP 531 000 B1 discusses an additive composition containing a.) a reaction product of a phosphorus or thiophosphorus acid with an ashless dispersant and a boron compound and b.) a sulfur containing antiwear-EP agent. The gear oil prepared with these components is said to have these performance improvements: 1.) inhibition of scoring/scuffing, 2.) improved wear in the form of ridging, rippling, pitting and spalling, 3.) improved oxidation in the form of reduced sludge and varnish deposits, especially at higher temperatures.
- The present inventors have surprisingly discovered a lubricant or grease composition which does not include primary, secondary, tertiary, cyclic aliphatic low molecular weight (<C30) monoamines or polyamines and/or the corresponding acid phosphate amine salts which, in preferred embodiments, exhibits improved performance in at least one of oxidative stability, seal compatibility, and anti-wear protection, while causing no significant deficits in other important areas of performance.
- The invention is directed to a lubricating fluid or grease, the improvement comprising the absence of primary, secondary, tertiary, and cyclic hydrocarbyl amines with a carbon number of less than C30 and the absence of the corresponding acid phosphate amine salts.
- In embodiments, the additive system used in the lubricating fluid is characterized by possessing a total base number (TBN) of less than 22.
- In an embodiment, the invention is further characterized as comprising an effective amount of an acid phosphate antiwear additive. In preferred embodiments, the phosphate antiwear additive will be at least one mono- and/or dialkyl acid phosphate effective for antiwear protection.
- Preferred mono- and/or dialkyl acid phosphates are represented by the formula (R1O)(R2O)P(O)OH, where R1 is hydrocarbyl and R2 is hydrocarbyl or hydrogen. R1 and R2 may have the same or different hydrocarbyl groups.
- The present invention is also directed to the use of such lubricating fluids and greases in gears, drives, axles, transmissions, and the like, in hydraulic and circulating systems, and in metal working. The invention is further directed to the use of apparatus comprising seals and lubricating fluids and/or greases in contact with said seals, the improvement comprising fluids and/or grease including the additive package in accordance with embodiments of the invention.
- It is an object of the invention to provide, in preferred embodiments, fully formulated lubricating fluids and greases having improvements in at least one of the properties of antiwear characteristics, oxidative stability, and seal performance.
- These and other objects, features, and advantages will become apparent as reference is made to the following detailed description, preferred embodiments, examples, and appended claims.
- In the accompanying drawings, like reference numerals are used to denote like parts throughout the several views.
-
FIG. 1 is a comparison of TBN for additive systems according to embodiments of the invention versus a commercial additive package. -
FIG. 2 is a comparison of the carbon varnish rating of formulations according to embodiments of the present invention versus comparative formulations. - According to the invention, a lubricating fluid or grease is provided without the use of primary, secondary, tertiary, or cyclic hydrocarbyl amine rust inhibitors with a carbon number of C30 or less, or the corresponding acid phosphate amine salts which, in certain embodiments, provides improvements in at least one of the areas of oxidation stability, seal compatibility and anti-wear performance, while causing no appreciable deficits in other areas of performance. More particularly, the invention relates to lubricating compositions useful in automotive gear boxes and differentials as well as industrial gear boxes.
- In preferred embodiments, fully formulated lubricating oils/greases and functional fluid compositions comprise an acid phosphate antiwear additive, preferably one or more hydrocarbyl or dihydrocarbyl acid phosphates, and there are essentially no acid phosphate hydrocarbyl amine salts, where the hydrocarbyl mono or polyamine is C30 or less, present in said fully formulated compositions. Until now, it has been believed that the stability of a phosphate-containing antiwear additive was dependent on the presence of this hydrocarbyl amine such that the phosphorus species is present, wholly or at least in part, as a salt of the amine with the acid phosphate. It is the surprising discovery of the present inventors that such is not the case. Moreover, improvements in certain important properties are evident in certain compositions according to embodiments of the present invention.
- It should be understood that in the expression “effective amount of an acid phosphate-containing antiwear additive”, both the “effective amount” and the identity of the acid phosphate-containing compound effective as an antiwear additive can readily be determined by one of ordinary skill in the art in possession of the present disclosure without more than routine experimentation.
- According to the invention, the term “phosphate” does not include any of the sulfur-containing compounds, e.g., thiophosphate compounds. In an embodiment, the acid phosphate may be present as the mono and/or dihydrocarbyl esters of the acid phosphate. The resulting gear lubricant is essentially free of hydrocarbyl primary, secondary, tertiary, and cyclic amine rust inhibitors with 30 carbons or less as an ingredient (when the invention is expressed as a “recipe” of ingredients) and therefore the final fully formulated lubricant is essentially free of the corresponding acid phosphate amine salts.
- In order to avoid misunderstanding, “essentially free of” allows for minor amounts, such as inevitable impurities which might lead to the presence of one or more of primary, secondary, tertiary, or cyclic aliphatic low molecular weight amines with 30 carbons (C30) or less and/or the presence of the corresponding acid phosphate amine salts but these ingredients and the constituents that form them are not present in an amount that might effect the novel and basic characteristics of the lubricating fluid.
- By omitting these amines from the additive concentrate and ultimately the lubricant, the additive system will have a significantly reduced total base number (TBN) for the package. The additive concentrates covered by this invention have a TBN<22, some cases less than 20, or less than 15, or less than 10, or even less than 5.
-
FIG. 1 is a plot of TBN and TAN (Total Acid Number) of a commercial additive package versus additive packages according to embodiments of the present invention. The commercial additive package was chosen because it has the lowest TBN in the population of commercial additive packages examined by the inventors. All other commercial packages tested by the inventors had higher TBN numbers. It is highly surprising that the additive packages according to embodiments of the present invention can provide the benefits set forth herein with low TBN in view of the TBN of prior art commercial products. - In addition, by omitting essentially all of the low molecular weight (≦C30) hydrocarbyl amine rust inhibitors from the gear lubricant, and therefore eliminating the resulting phosphate amine salts, a number of very important performance benefits may be achieved in embodiments, which in preferred embodiments contribute enhanced durability.
- The first of these performance benefits is enhanced antiwear performance. As discussed in the experimental section below, testing according to the industry-recognized L-37 rig test (ASTM D6121) has shown significant improvements particularly in the low temperature version (conventionally known as the “Canadian version”) of this test.
- Also, in embodiments, the oxidative stability of gear oils without the hydrocarbyl amine rust inhibitor described earlier is superior to those with such an amine present. It has been shown that when the low molecular (≦C30) hydrocarbyl amines are eliminated from a gear lubricant, the oxidation performance is dramatically improved. This can be demonstrated using the industry oxidation test called the L-60-1 (ASTM D5704).
- Improved seal performance was also noted from a gear lubricant formulated in accordance with the invention. The ASTM D5562 static seal test was run using both fluoroelastomer (Viton) and polyacrylate seal materials. In both tests, the elongation percent loss was significantly reduced.
- It has been expected that fluids formulated without low molecular weight hydrocarbyl amine rust inhibitors would be deficient in the area of rust inhibition. In embodiments of the invention, the rust performance of gear lubricants prepared within the scope of the invention was evaluated using the automotive gear industry's L-33 test (ASTM D7038). The results surprisingly demonstrate that fluids formulated in this manner had no steel corrosion deficiencies.
- It is preferred that the finished gear lubricant according to embodiments of the present invention also include at least one of the ingredients from the group consisting of: a sulfur-containing extreme pressure (EP) agent, a nitrogen-containing dispersant, and a corrosion inhibitor. Other preferred additives may include at least one ingredient selected from the group consisting of: borated dispersants, non-aminic rust inhibitors, defoamants, pour point depressants, antioxidants, demulsifiers, friction modifiers, seal swell agents, chromophores, deodorants, limited slip additives, detergents, and tackifiers.
- In an embodiment, the invention is directed to a lubricant comprising a major amount of an oil of lubricating viscosity and a minor amount of at least one substituted phosphoric acid composition characterized by the formula (R1O)(R2O)P(O)OH, where R1 is a hydrocarbyl group and R2 is either hydrogen or a hydrocarbyl group.
- The term “major amount” means present in an amount greater than any other ingredient, based on wt. %. The “oil of lubricating viscosity” will also be described as a “base oil” herein, and may be a combination of one or more base oils, with the term “major amount” meaning the sum of the base oils are present in an amount greater than any other ingredient.
- The lubricant composition preferably will also contain a sulfur-containing extreme pressure agent.
- The lubricant composition preferably also will contain nitrogen-containing dispersants and corrosion inhibitors, with the proviso that said species not include low molecular weight primary, secondary, tertiary, or cyclic aliphatic mono and/or polyamines with 30 carbons or less.
- The products according to embodiments of the invention may be used for a wide variety of automotive and industrial gear applications. Examples of such applications include use in hypoid axles and in mechanical steering drives in passenger cars and in cross-country vehicles. In addition, the products based on embodiments of the present invention may be used in planetary hub reduction axles, mechanical steering and transfer gear boxes in utility vehicles such as trucks. It also can be used in different types of gear boxes, e.g. synchromesh gear boxes, as well as power take-off gears, limited slip axles, and Planetary hub reduction gear boxes.
- The lubricating oil and functional fluid compositions according to embodiments of the present invention are based on diverse oils of lubricating viscosity, including natural and synthetic lubricating oils and mixtures thereof. These lubricating compositions are particularly effective as gear lubricants for both industrial and automotive gear applications, but could also be considered for other lubricant applications, e.g. hydraulic, metal working, turbine, circulating, and small engine.
- Compositions according to embodiments of the invention may further comprise one or more base oils. It will be recognized that in certain instances it may be convenient to have a lubricant composition which is not completely formulated, i.e., with a minor amount of additives left to be added by the final end consumer, for the purposes of the present disclosure a “fully formulated” lubricant composition means that any additional components to be added do not affect the novel and basic characteristics of the lubricant according to the present invention.
- Fluids that can meet the criteria of base oil for lubricant and functional fluids are varied. They may fall in any of the well-known American Petroleum Institute (API) categories of Group I through Group V. The API defines Group I stocks as solvent-refined mineral oils. Group I stocks contain the most unsaturates and sulfur and have the lowest viscosity indices. Group I defines the bottom tier of performance. Group II and III stocks are high viscosity index and very high viscosity index base stocks, respectively. The Group III oils contain the lowest level of unsaturates and sulfur relative to Group I and II oils. With regard to certain characteristics, both Group II and Group III oils perform better than Group I, particularly in the area of oxidative stability and low temperature performance.
- Group IV stocks consist of polyalphaolefins, which can be produced via the catalytic oligomerization of linear alphaolefins (LAOs), with particularly preferable LAOs selected from C5-C14 linear alphaolefins, more preferably from 1-hexene to 1-tetradecene, more preferably from 1-octene to 1-dodecene, and mixtures thereof, although oligomers of lower olefins such as ethylene and propylene, oligomers of ethylene/butene-1 and isobutylene/butene-1, oligomers of ethylene with other higher olefins, such as described in U.S. Pat. No. 4,956,122, and the patents referred to therein, and the like, may also be used. PAOs typically offer superior volatility, thermal stability, and pour point characteristics to those base oils in Group I, II, and III.
- Group V includes all the other base stocks not included in Groups I through IV. Group V base stocks include, e.g., esters, alkylated aromatics, polyinternal olefins (PIOs), polyisobutylenes, polyalkylene glycols (PAGs), etc.
- One of the benefits of embodiments of the present invention is that it may be applicable to base oils fitting into any of the above five categories, API Groups I to V, as well as other materials.
- In preferred embodiments, the lubricating compositions of the invention comprise an additive system which includes ingredients selected from the group consisting of: one or more sulfur-containing extreme pressure agents, one or more acid phosphates (pentavalent phosphorus), one or more ashless dispersants, one or more corrosion inhibitors, and optionally anti-foamants, pour point depressants, friction modifiers, demulsifiers, tackifiers, VI improvers, deodorants, seal swell agents, and non-amine rust inhibitors, and mixtures thereof, with the proviso that it is essentially free of: (a) low molecular weight (C30 or less) primary, secondary, tertiary, and cyclic hydrocarbyl amines; and (b) the corresponding acid phosphate amine salts.
- While each of the aforementioned ingredients are per se known in the art, preferred embodiments are discussed in more detail below.
- Extreme Pressure Agents
- Extreme pressure (EP) agents used in the composition according to embodiments of the invention include sulfur-containing and boron-containing EP agents. Sulfur-containing EP agents are preferred.
- Sulfurized olefins may be useful in providing protection against high pressure, metal-to-metal contacts in industrial and automotive gear oils. There is no particular restriction on the sulfur-containing extreme pressure additive that can be used in the additive package. Sulfur-containing components useful in this regard included sulfurized olefins, dialkyl polysulfides, diarylpolysulfides, sulfurized fats and oils, sulfurized fatty acid esters, trithiones, sulfurized oligomers of C2-C8 monoolefins, thiophosphoric acid compounds, sulfurized terpenes, thiocarbamate compounds, thiocarbonate compounds, sulfoxides, and thiol sulfinates. Mixtures of sulfur-containing EP components may be used.
- The preferred sulfur-containing EP components are selected from sulfurized oligomers of C2-C8 monoolefins, olefins sulfides, and dialkyl and diaryl polysulfides. The more preferred extreme pressure agents are oligomeric olefin sulfides and dialkyl polysulfides. In the most preferred embodiment, the sulfurized olefin is prepared via a high pressure sulfurization procedure.
- For some gear oil applications, it is possible that boron-containing EP additives may be adequate, provided that significant amounts of water are not present to cause hydrolysis. Use of boron-containing EP agents alone or with sulfur-containing EP agents are both contemplated. However, in preferred embodiments, the composition does not use an extreme pressure ingredient containing boron.
- Dispersants
- Dispersants serve inter alia to keep sludge and varnish particles from coating on the gear surfaces. There are no particular restrictions on the type used, though it is preferable that at least one contains nitrogen. Nitrogen-containing dispersants include alkyl succinimides, alkenyl succinimides, benzylamine compounds (Mannich bases), polybutenylamines, and the like. Borated versions of any of these are optional.
- In some preferred embodiments, nitrogen-containing dispersants are selected from alkyl succinimides and alkenyl succinimides. The especially preferred ashless dispersant for use in this invention are the products of reaction of a polyethylene polyamine, e.g. tetraethylene pentamine, with a hydrocarbon-substituted anhydride made by the reaction of a polyolefin, preferably having a molecular weight of about 700-5000 and especially 800-3000 (it is not particularly important whether this is number average molecular weight or weight average molecular weight) with an unsaturated polycarboxylic acid or anhydride, e.g. maleic anhydride.
- Borated dispersants are optional and may be formed by borating ashless dispersants using suitable boron-containing compounds: boron acids, boron oxides, boron esters, and amine or ammonium salts of boron acids.
- Corrosion Inhibitors/Metal Passivators
- Corrosion inhibitors or metal passivators are typically additives that are heterocyclic in nature and are nitrogen-, and optionally, sulfur-containing. Triazole and its derivatives have been found to prevent corrosion in gear oils. Some specific examples include benzotriazole, tolyltriazole, 2-mercaptotriazole, dodecyltriazole. Alkyl and aryl derivatives are preferred.
- A specific class of passivators is known as “copper passivators.” These comprise a class of compounds which includes thiadiazoles, triazoles, and thiazoles. The preferred compounds are the 1,3,4-thiadiazoles.
- Phosphate Anti-Wear Agents
- In preferred embodiments, an effective amount of at least one mono- and/or dialkyl acid phosphate for antiwear protection. Preferred mono- and/or dialkyl acid phosphates antiwear additives include at least one species represented by the formula (R1O)(R2O)P(O)OH, where R1 is hydrocarbyl and R2 is hydrocarbyl or hydrogen. R1 and R2 may have the same or different hydrocarbyl groups. Suitable hydrocarbyl groups have 1-40 carbon atoms, preferably 2-20 and more preferably 3-20. The preferred acid phosphates are selected from mono- and di-2-ethylhexyl acid phosphates and mixtures thereof.
- Acid phosphates would be preformed salts comprising the acid phosphate and a low molecular weight hydrocarbyl amine or the acid phosphate salt would be formed in situ in the additive package or the finished lubricant or grease (or at some other point between prior to or even during actual use). Such salts are described in, e.g., U.S. Pat. Nos. 2,063,629, 2,224,695, 2,447,288, 2,616,905, 3,728,260, 3,984,448, and 4,431,552. The hydrocarbyl amine is often termed a “rust inhibitor” and is usually a low molecular weight (, less than or equal to C30, i.e., ≦C30) primary or secondary, mono or polyamine, but could also be tertiary or cyclic mono/polyamines. The preferred amines are generally aliphatic in nature and possess from 4-30 carbon atoms. Some specific examples include the following: octylamine, decenylamine, dodecenylamine, oleylamine, and the like. Typically, the most preferred amines are described as a complex with acid phosphates, where the aliphatic group of the amine is a tertiary alkyl group and the amine is a primary amine. Primene 81-R and Primene JMT amines are typically describes as most preferred.
- The present inventors have surprisingly found that by eliminating essentially all of the low molecular weight hydrocarbyl amine “rust inhibitors”, and (without wishing to be bound by theory) the corresponding acid phosphate salt complex, the additive system will still possess adequate rust performance, even without the addition of other rust inhibitors and will also have, in at least some embodiments, at least one improved property selected from oxidation stability, seal compatibility and antiwear protection.
- Optional additives that may be included in the additive concentrate or the lubricating composition include: defoamants, non-aminic rust inhibitors, seal swell agents, friction modifiers, antioxidants, deodorants, chromophores, pour point depressants, tackifiers, demulsifiers, detergents, VI modifiers, and mixtures thereof. One of ordinary skill in the art, in possession of the present disclosure, can determine the nature and quantity of additives to provide in the fully formulated lubricant or grease without undue experimentation.
- It should be noted that various ingredients may combine with the other ingredients to form salts, adducts, coordinated species, and the like. The combination of such species may be formed prior to addition to the final lubricant fluid (e.g., in an additive package), they may be formed in situ with a small amount of diluent (typically the final basestock) or they may be formed in situ after the ingredients are added to the basestock. Various combinations are possible. With this in mind, the present disclosure thus should be read in the nature of a recipe as regards the various additive described herein.
- Furthermore, although all ingredients added to the final fully formulated lubricating fluid or greases described herein may be provided in a single additive package, the term “additive package” should be taken to mean any one additive package used or the entire sum of ingredients added to the one or more base oils used to create the final fully formulated composition.
- The following examples are meant to illustrate the present invention and provide a comparison with lubricant formulation which, although heretofore considered adequate for commercial purposes, are not prepared in accordance with the present invention. While the examples of the invention are described with particularity, they should not be taken to limit the invention. Rather, numerous variations or modifications will become apparent to (and can be readily made by) those of ordinary skill in the art in light of these examples, particularly when viewed together with the entire disclosure.
- For automotive applications, the oils were tested in the rig tests that are incorporated into API and SAE standards GL-5 and J2360, respectively. The L-37 test was used to assess antiwear performance; the L-60-1 was used for oxidative and thermal stability; and the static seal test ASTM D5662 was run for polyacrylate and fluoroelastomer seal compatibility. The L-42 for protection against scoring and the L-33 and ASTM D130 for corrosion protection were also run to demonstrate no deficiencies as a result of amine elimination. For industrial gear oils, the ASTM D2783 Four Ball EP test and ASTM D665 for rust were run.
- To evaluate a gear lubricant according to the present invention, the axle test ASTM D6121 was employed. This particular test is more commonly known as the L-37 test and is used in the industry to evaluate the antiwear performance of an automotive gear lubricant. This test method measures a lubricant's ability to protect final drive axles from abrasive wear, adhesive wear, plastic deformation, and surface fatigue, when subjected to low-speed high-torque conditions. Lack of protection can lead to premature gear or bearing failure or both.
- The test apparatus is a new, complete hypoid truck axle assembly,
Dana Model 60 with 5.86 to 1 ratio. The assembly is mounted on a test stand with the pinion and axle shafts' center lines horizontal. The gears are first run through a conditioning phase and then through a test phase. The test phase is 24 h+0.2 h and is run at 275° F. with a load of 1740 ft-lb on each wheel and 80 rpms/min. At the end of the test, the differential is disassembled and the ring gear and pinion are inspected and rated for each type of distress (e.g. spalling, pitting, ridging, wear, rippling, etc.). The rating value is reported. - This same test method is also used for the Canadian version of the test, known as the Low Temperature (LT) L-37. The LT L-37 axle test is required for 75W gear oils. This procedure is identical to the regular temperature L-37, except that the temperature of the test is run approximately 55° F. lower during both the conditioning and gear test phase.
- The oxidative and thermal stability were evaluated in ASTM D5704 or the L-60/L-60-1 test, which is the most common test procedure for evaluating these features of automotive gear oils. The test covers the oil-thickening and insolubles/deposit formation characteristics of the lubricant when subjected to high temperature oxidizing conditions. For the L-60 test, the candidate lubricant is heated to 325° F./163° C. for 50 hr in a small gear box with two lightly loaded spur gears. Air is bubbled through the oil at a rate of 1 L/hr. The viscosity of the oxidized oil is measured at the end of the test and compared to the initial value. The pentane and toluene insolubles are also measured. The L-60-1 test is run in the same manner; however, the carbon-varnish and sludge are measured along with the insolubles and the viscosity increase.
- For seal compatibility, ASTM D5662 was run. This is a laboratory test method which evaluates gear oils for compatibility with various elastomers: nitrile, polyacrylate, and fluoroelastomer. This method addresses failures that may be caused by excessive elastomer hardening, elongation loss, and volume swell and attempts to determine the likelihood that an oil might cause premature sealing system failures in the field. Specimens are cut from the elastomer being evaluated and are immersed in oil for 240 hr. Reference oils are run periodically. The test temperature is dependent on the type of seal material used: 100° C. for nitrile and 150° C. for fluoroelastomer and polyacrylate. At the end of 240 hr, the aged elastomer specimens are tested for changes in hardness, elongation, tensile strength and volume.
- Lubricating compositions, Oils A1 and A2 were prepared in accordance with embodiments of the invention whereas Oils X1 and X2 were formulated for comparison. The contents of these fluids are shown in Table 1 below. The additive systems of all examples use identical components, differing only in percentages. The additive percentages of X1 and X2 were manipulated to provide the closest approach to the percent of S, P, and N additives in A1 and A2, respectively, which is believed to provide the most valid comparison. The key difference between A1 and X1, and between A2 and X2, is the omission of the hydrocarbyl primary amine rust inhibitor in examples A1 and A2. The TBNs for the additive concentrates were calculated using a potentiometric method ASTM D 2896. Oils A1 and A2 have a TBN=14.8 and Oils X1 and X2 have TBN=27.9.
TABLE 1 Embodiment of Comparison Embodiment of Comparison the Invention Example the Invention Example Oil Code Test A1 X1 A2 X2 Additives in Finished Fluid, wt % EP Agent, Mobilad C-175 3.65 4.24 3.65 4.24 Antiwear - Mobilad C-421 - Acid Phosphate 1.13 1.37 1.13 1.37 Amine Rust Inhibitor - Primary Amine (<C30) 0 0.59 0 0.59 Dispersant, Borated and non-borated 3.51 2.00 3.51 2.00 Copper Passivator - thiadiazole 0.54 0.25 0.54 0.25 Other additives (inhibitors, antioxidants, defoamants) 1.19 1.19 1.19 1.19 TBN of Additive System ASTM D2896 14.8 27.9 14.8 27.9 S in Finished Oil 2.07 2.19 1.95 2.190 P in Finished Oil 0.128 0.157 0.125 0.158 N in Finished Oil 0.14 0.14 0.14 0.11 Basestocks, wt % PAO 2, 6 cSt 20.0 20.4 26.0 26.4 PAO 150 55.0 55.0 44.0 44.0 Isononyl Heptanoate 15.0 15.0 20.0 20.0 Viscometrics of Finished Fluid KV 100° C., cSt ASTM D445 19.65 18.04 11.8 11.3 VI ASTM D2270 216 219 226 229 Brookfield at −40° C., cP ASTM D2983 21,495 17,300 7,318 6,470 - In the actual L-60-1 test, Oils A1 and A2 had much improved carbon-varnish ratings compared with Oil X1 and Oil X2. The results are shown in Table 2. Based on this test alone, the ratings results for Oils X1 and X2 are considered as “failing”.
FIG. 2 shows graphically the superior C-V performance of the candidate oils. Since the cleanliness is related to the C-V rating, it can be stated that the oils are cleaner. Pentane and toluene insolubles were non-existent for Oils A1 and A2 but around 0.3-0.4 mass percent for the oils X1 and X2. The sludge rating for all four oils was not significantly different. - An improvement in the seal compatibility was also observed for Oils A1 and A2 relative to Oil X2 in the seal test ASTM D5662 (testing of X1 was considered superfluous on the basis of the results for X2). The change in percent elongation was reduced for both the fluoroelastomer and polyacrylate with Oils A1 and A2 (see Table 2 for data), which implies that the candidate oils are having less affect on the elastomer than the comparative Oil X2.
- The oils were evaluated in the ASTM D130 Copper Corrosion Test as well as in the L-33 Rust Test. The copper strip was rated 1b for all four oils. It is somewhat surprising that formulations without the aminic rust inhibitor achieves the same result as the commercially acceptable formulations with the rust inhibitor. In the L-33 test, all formulations were well above the pass/fail line of 9.0 as referenced in SAE J2360 (see Table 2 for data).
- The L-42 test is used for determining the anti-scoring properties of gear lubricants under high speed and shock conditions. It is described as having the same effect on gears as the start of a drag race. The test unit consists of Dana rear axle 44-1 with a gear ratio of 45:11. In a similar fashion as the L-37 test, the gears are mounted on a test stand with the pinion and axle shafts' center lines horizontal. The gears are put through a series of accelerations and decelerations against dynamometers under specified conditions of speed and torque for four cycles. The gear teeth are inspected at the end of the test for the amount of scoring on the tooth surface. The amount of scoring must be less than or equal to the pass reference oil. Both oils were tested and the data are presented in Table 2. Oils A1 and A2 had acceptable performance, proving the absence of low molecular weight hydrocarbyl amine does not hurt scoring performance.
- These data reveal that the automotive gear oils formulated in accordance with embodiments of this invention had excellent performance, despite missing the rust inhibitor. Performance was better in areas of oxidation, anti-wear and seal performance and in areas that one might expect to be problematic, e.g. rust and copper corrosion, was not affected significantly.
TABLE 2 Embodiment of Comparison Embodiment of Comparison the Invention Example the Invention Example Oil Code Test A1 X1 A2 X2 Copper Corrosion ASTM D130 1b 1b 1b 1b L-37 Test, Uncoated Gears ASTM D6121 Pinion Ring Pinion Ring Pinion Ring Pinion Ring Burnish 5 5 5 5 5 5 5 5 Discoloration 6 6 6 6 6 7 6 7 Corrosion 10 10 10 10 10 10 10 10 Deposits 10 9 10 10 10 10 9 9 Wear 6 8 6 7 7 7 6 7 Scoring 10 10 10 10 10 10 10 10 Rippling 8 9 8 9 9 9 8 9 Ridging 8 9 8 9 9 10 8 9 Spitting 9.9 9.9 9.9 9.9 9.9 9.9 9.9 9.9 Overall Merit 8.94 8.92 9.41 8.92 Evaluation Pass Pass Pass Pass L-37 Test, Uncoated Gears, Low Temp. ASTM D6121 Pinion Ring Pinion Ring Pinion Ring Pinion Ring Burnish 5 5 5 5 5 5 3 5 Discoloration 6 6 6 6 6 7 6 6 Corrosion 10 10 10 10 10 10 10 10 Deposits 10 9 10 7 10 9 10 8 Wear 6 8 5 6 6 8 5 6 Scoring 10 10 10 10 10 10 10 10 Rippling 9 10 7 9 9 9 6 9 Ridging 9 10 6 6 9 10 6 6 Spitting 9.9 9.9 8.0 9.9 9.9 9.9 9.0 9.9 Overall Merit 9.56 7.66 9.41 7.66 Evaluation Pass Fail Pass Fail L-60-1 Test (n = 1) ASTM D5704 % Viscosity Increase 35 22 27 18 Pentane Insolubles 0 0.40 0 0.35 Toluene Insolubles 0 0.41 0 0.37 Carbon/Varnish 9.7 5.8 9.8 5.0 Sludge 9.5 9.62 9.7 9.49 Evaluation Pass Fail Pass Fail L-42 % Scoring Ring, Coast 4 3 4 5 % Scoring Pinion, Coast 6 5 9 8 % of Pass/Fail Reference 26 24 33 32 Evaluation Pass Pass Pass Pass Seal Compatibility ASTM D5662 Fluoroelastomer, % elongation change −14.7 nd −12.7 −34.9 Polyacrylate, % elongation change 11.0 nd 28.0 70.5 Nitrile, % elongation change −55.8 nd −53.4 −56.6 L-33-1 Test ASTM D7038 Merit Rating 9.31 9.91 9.56 9.83 Evaluation Pass Pass Pass Pass - Industrial Gear Fluids
- Industrial gear fluids were also formulated in accordance with embodiments of the present invention and one was tested in an effort to demonstrate acceptable performance despite the omitted low molecular weight (less than or equal to C30) hydrocarbyl amine and the corresponding phosphate amine salt. Oil B was one such candidate, i.e. no low molecular weight (≦C30) hydrocarbyl amine was part of the additive system. Here again, the additive package's TBN was unusually low, measured at 4.5. Table 3 below shows the composition of the additive system and the mineral base oils that were employed.
TABLE 3 Embodiment of Comparison the Invention Example Oil Code Test B Y Additives in Finished Lubricant, wt % EP Agent, Mobilad C-170 0.56 0.56 Antiwear - Mobilad C-421 - Acid Phosphate 0.37 0.37 Amine Rust Inhibitor - Primary Amine (<C30) 0 0.12 Dispersant, Borated and non-borated 0.09 0.09 Copper passivator - thiadiazole 0.20 0.09 Other additives (inhibitors, defoamants, demulsifiers) 0.046 0.046 TBN of Additive System ASTM D2896 4.5 27.8 S in Finished Oil (additive contribution only) 0.275 0.275 P in Finished Oil 0.0440 0.044 N in Finished Oil 0.017 0.015 Basestocks, wt % 150″ Solvent Paraffinic Neutral 12.5 12.5 150 Bright Stock 86.0 86.0 Viscometrics KV, 100° C. ASTM D445 23.6 23.7 KV, 40° C. ASTM D445 306.3 309.3 VI ASTM D2270 97 97 - To evaluate the performance of an industrial gear lubricant prepared in accordance with embodiments of the invention, laboratory bench tests that are part of AIST 224 (formerly USS 224), AGMA 9005-E02, and other common industry specifications, were employed. Again, antiwear performance and rust protection were evaluated. ASTM D2783, a Four Ball EP Load Wear Test, measures the antiwear capability of the gear lubricant. One steel ball under load is rotated against three stationary balls immersed in oil. The load is increased until the weld point in kilograms is determined. The load wear index, an index of the ability of the lubricant to minimize wear at applied loads, is also measure. ASTM D4172 uses the Four Ball Test Machine to assess the wear preventive characteristics of lubricating fluids. A steel ball is rotated atop of three clamped balls at a rate of 1800 rpms for 60 minutes under a force of 20 kg at 75° C. The average wear scar of the three clamped balls is then determined. ASTM D665 is used to measure protection from steel corrosion. A mixture of test oil is mixed with either distilled water (Part A) or synthetic sea water (Part B) at a temperature of 60° C. with a cylindrical steel rod completely immersed. After four hours, the test rod is examined for signs of rusting. Copper corrosion performance was roughly equivalent for the two oils as determined by ASTM D130. The results for Oil B and comparison Oil Y are shown in Table 4.
TABLE 4 Embodiment of Comparison the Invention Example Oil Code Test B Y Copper Corrosion ASTM D130 1a 1b Four Ball Wear ASTM D4172 Wear Scar, mm 0.31 0.35 Four Ball Weld ASTM D2783 Load Wear Index, kg 53 63 Weld Point, kg 250 250 Rust Test ASTM D665 Part A Pass Pass Part B Pass Pass - From these results, one can see there is no significant detrimental effect for this industrial gear oil when the hydrocarbyl amine rust inhibitors are omitted from the package. The rust test ASTM D665 is readily passed with both distilled and salt water. Copper corrosion protection is also satisfactory for the candidate fluid based on ASTM D130 results. The antiwear performance is roughly equivalent as evidenced by the Four Ball Wear and EP test results.
- The invention has been described above with reference to numerous embodiments and specific examples. Many variations will suggest themselves to those skilled in this art in light of the above detailed description. All such obvious variations are within the full intended scope of the appended claims. Nevertheless, several particularly preferred embodiments may be pointed out.
- Preferred embodiments include a fully formulated lubricating fluid or grease including an effective amount of an acid phosphate-containing antiwear additive, characterized as comprising an additive package and a major amount of at least one base oil, the improvement comprising the absence of low molecular weight primary, secondary, tertiary, and cyclic aliphatic amines of 30 carbons or less and the absence of the corresponding acid phosphate amine salts, with still more preferred embodiments, which may be combined as would be recognized by one of ordinary skill in the art in possession of the present disclosure, selected from: (i) wherein said additive package has a TBN<22 (or TBN<20, or TBN<15, or TBN<10, or TBN<5; (ii) wherein said acid phosphate is selected from at least one mono and/or dihydrocarbyl ester of an acid phosphate characterized by the formula (1): (R1O)(R2O)P(O)OH, where R1 is a hydrocarbyl group and R2 is selected from hydrogen or a hydrocarbyl group, particularly wherein the hydrocarbyl groups of R1 and R2 are independently selected from straight-chained or branched alkyl groups having from 1 to 20 carbon atoms, or from 2 to 20 carbon atoms, or from 3 to 20 carbon atoms, any of which may be modified by the further limitation that at least one of R1 and R2 is 2-ethylhexyl; (iii) further characterized as comprising at least one of the following ingredients: (a) at least one sulfur-containing extreme pressure agent; (b) at least one nitrogen-containing dispersant; (c) at least one corrosion inhibitor; (iv) further comprising at least one ingredient selected from the group consisting of borated dispersants, non-aminic rust inhibitors, defoamants, pour point depressants, antioxidants, demulsifiers, friction modifiers, seal swell agents, chromophores, deodorants, limited slip additives, detergents, VI modifiers, and tackifiers; (v) further characterized by a major amount of at least one base oil selected from API Groups I to V; (vi) further characterized by at least one of the following criterion: (a) rated 1a or 1b according to the Copper Corrosion test according to ASTM D130; (b) passing the Four Ball Weld test according to ASTM D2783 with a Weld Point of 250 kg minimum and a Load Wear Index of 45 kg minimum; (c) passing the Rust Test, Part A and Part B, according to ASTM D665; (d) having a value of at least 9.0 or greater in the L33 test, run according to ASTM D7038.
- Another preferred embodiment is an apparatus comprising at least one seal and a lubricating fluid or grease in contact with said seal, wherein said lubricating fluid or grease is that characterized in the previous paragraph, particularly an apparatus wherein the seal comprises at least one material selected from fluoroelastomers, nitrites, and polyacrylates, and also particularly wherein the apparatus, which may have the seal as just described, comprises at least one of the following: a hypoid axle, a mechanical steering drive or gear box, a planetary hub reduction axle or gear box, a transfer gear box, a synchromesh gear box, a power take-off gear, a limited slip axle, an engine or turbine, a hydraulic system.
- Still other particularly preferred embodiments are: a process for metal working or in a circulating fluid system, either comprising the use of a lubricant or grease, the improvement comprising the use of the lubricating fluid or grease as described in the paragraph just above the immediately preceding paragraph.
- Yet still another particularly preferred embodiment is a fully formulated lubricating fluid or grease suitable for use in driveline fluids and/or gear boxes for industrial applications comprising an additive package and a major amount of at least one base oil and essentially free of low molecular weight primary, secondary, tertiary, and cyclic aliphatic amines of 30 carbons or less and their corresponding acid phosphate salts, which may be modified in numerous ways described herein, particularly in any of the ways described in paragraph [00112], but in the important embodiment which may be characterized as containing an acid phosphate selected from at least one mono and/or dihydrocarbyl ester of an acid phosphate characterized by the formula (1): (R1O)(R2O)P(O)OH, where R1 is a hydrocarbyl group and R2 is selected from hydrogen or a hydrocarbyl group, especially wherein at least one of R1 and R2 is 2-ethylhexyl.
- Moreover, a particularly preferred embodiment also is a method for lubricating an apparatus, the method comprising applying a lubricant to the apparatus wherein said lubricant comprises a base oil, an effective amount of an acid phosphate-containing antiwear additive, said lubricant further characterized as essentially free of primary, secondary, tertiary and cyclic hydrocarbyl amines with a carbon number of C30 or less and the corresponding salts of said acid phosphate, which may of course be modified by any one or more of the limitations set forth in paragraph [00112].
- Unless stated otherwise herein, the meanings of terms used herein shall take their ordinary meaning in the art; reference shall be taken, in particular, to Synthetic Lubricants and High-Performance Functional Fluids, Second Edition, Edited by Leslie R. Rudnick and Ronald L. Shubkin, Marcel Dekker (1999). This reference, as well as all patents and patent applications, test procedures (such as ASTM methods and the like), and other documents cited herein are fully incorporated by reference to the extent such disclosure is not inconsistent with this invention and for all jurisdictions in which such incorporation is permitted. Note that Trade Names used herein are indicated by a ™ symbol or ® symbol, indicating that the names may be protected by certain trademark rights, e.g., they may be registered trademarks in various jurisdictions. Note also that when numerical lower limits and numerical upper limits are listed herein, ranges from any lower limit to any upper limit are contemplated.
Claims (28)
(R1O)(R2O)P(O)OH (1)
(R1O)(R2O)P(O)OH (1)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/333,689 US20070167334A1 (en) | 2006-01-17 | 2006-01-17 | Lubricating fluids |
PCT/US2006/043906 WO2007084208A1 (en) | 2006-01-17 | 2006-11-13 | Lubricating fluids |
US12/961,624 US20110111992A1 (en) | 2006-01-17 | 2010-12-07 | Lubricating fluids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/333,689 US20070167334A1 (en) | 2006-01-17 | 2006-01-17 | Lubricating fluids |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/961,624 Continuation-In-Part US20110111992A1 (en) | 2006-01-17 | 2010-12-07 | Lubricating fluids |
Publications (1)
Publication Number | Publication Date |
---|---|
US20070167334A1 true US20070167334A1 (en) | 2007-07-19 |
Family
ID=36764559
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/333,689 Abandoned US20070167334A1 (en) | 2006-01-17 | 2006-01-17 | Lubricating fluids |
Country Status (2)
Country | Link |
---|---|
US (1) | US20070167334A1 (en) |
WO (1) | WO2007084208A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106479622A (en) * | 2016-08-26 | 2017-03-08 | 广州吉盛润滑科技有限公司 | A kind of mixing ester type combination of oil for pair of gear worm and its preparation method and application |
Citations (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2224695A (en) * | 1938-11-25 | 1940-12-10 | Carl F Prutton | Inhibitor |
US2692859A (en) * | 1951-07-18 | 1954-10-26 | Shell Dev | Metal-working lubricant |
US3513093A (en) * | 1963-06-17 | 1970-05-19 | Lubrizol Corp | Lubricant containing nitrogen-containing and phosphorus-containing succinic derivatives |
US3728260A (en) * | 1969-10-24 | 1973-04-17 | Exxon Research Engineering Co | Additive for lubricating composition |
US4118328A (en) * | 1977-12-08 | 1978-10-03 | Chevron Research Company | Amine phosphate salts |
US4431552A (en) * | 1982-11-26 | 1984-02-14 | Chevron Research Company | Lubricant composition containing an alkali-metal borate and a mixture of phosphates, monothiophosphates and dithiophosphates in a critical ratio |
US4575431A (en) * | 1984-05-30 | 1986-03-11 | Chevron Research Company | Lubricant composition containing a mixture of neutralized phosphates |
US4900460A (en) * | 1988-08-02 | 1990-02-13 | Mobil Oil Corp. | Sulfurized olefin adducts of dihydrocarbyl phosphates and phosphites and lubricant compositions containing same |
US5064546A (en) * | 1987-04-11 | 1991-11-12 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
US5328619A (en) * | 1991-06-21 | 1994-07-12 | Ethyl Petroleum Additives, Inc. | Oil additive concentrates and lubricants of enhanced performance capabilities |
US5354484A (en) * | 1986-06-13 | 1994-10-11 | The Lubrizol Corporation | Phosphorus-containing lubricant and functional fluid compositions |
US5358650A (en) * | 1993-04-01 | 1994-10-25 | Ethyl Corporation | Gear oil compositions |
US5500140A (en) * | 1995-03-31 | 1996-03-19 | Ethyl Corporation | Oil-soluble phosphorus- and nitrogen-containing additives |
US5547596A (en) * | 1993-05-25 | 1996-08-20 | Idemitsu Kosan Co., Ltd. | Lubricant composition for limited slip differential of car |
US5573696A (en) * | 1995-03-31 | 1996-11-12 | Ethyl Corporation | Oil-soluble phosphorus- and nitrogen-containing additives |
US5691283A (en) * | 1994-03-01 | 1997-11-25 | Ethyl Petroleum Additives Limited | Use of transmission and gear oil lubricants having enhanced friction properties |
US5756429A (en) * | 1993-10-06 | 1998-05-26 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition for high-speed gear |
US5763372A (en) * | 1996-12-13 | 1998-06-09 | Ethyl Corporation | Clean gear boron-free gear additive and method for producing same |
US5792733A (en) * | 1997-08-14 | 1998-08-11 | The Lubrizol Corporation | Antiwear compositions containing phosphorus compounds and olefins |
US5942470A (en) * | 1990-05-17 | 1999-08-24 | Ethyl Petroleum Additives, Inc. | Lubricant compositions |
US6043200A (en) * | 1995-07-31 | 2000-03-28 | Exxon Chemical Patents, Inc. | Oleaginous compositions |
US6046144A (en) * | 1997-06-02 | 2000-04-04 | R.T. Vanderbilt Co., Inc. | Combination of phosphate based additives and sulfonate salts for hydraulic fluids and lubricating compositions |
US20030144157A1 (en) * | 2001-10-23 | 2003-07-31 | Idemitsu Kosan Co., Ltd. | Oil composition for heat treatment of a gear and gear treated by using the oil composition |
US6844300B2 (en) * | 2001-02-20 | 2005-01-18 | Ethyl Corporation | Low phosphorus clean gear formulations |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3184113B2 (en) * | 1997-03-24 | 2001-07-09 | 東燃ゼネラル石油株式会社 | Lubricating oil composition for automatic transmission |
EP1090096A1 (en) * | 1998-06-01 | 2001-04-11 | Castrol Limited | A functional fluid |
-
2006
- 2006-01-17 US US11/333,689 patent/US20070167334A1/en not_active Abandoned
- 2006-11-13 WO PCT/US2006/043906 patent/WO2007084208A1/en active Application Filing
Patent Citations (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2224695A (en) * | 1938-11-25 | 1940-12-10 | Carl F Prutton | Inhibitor |
US2692859A (en) * | 1951-07-18 | 1954-10-26 | Shell Dev | Metal-working lubricant |
US3513093A (en) * | 1963-06-17 | 1970-05-19 | Lubrizol Corp | Lubricant containing nitrogen-containing and phosphorus-containing succinic derivatives |
US3728260A (en) * | 1969-10-24 | 1973-04-17 | Exxon Research Engineering Co | Additive for lubricating composition |
US4118328A (en) * | 1977-12-08 | 1978-10-03 | Chevron Research Company | Amine phosphate salts |
US4431552A (en) * | 1982-11-26 | 1984-02-14 | Chevron Research Company | Lubricant composition containing an alkali-metal borate and a mixture of phosphates, monothiophosphates and dithiophosphates in a critical ratio |
US4575431A (en) * | 1984-05-30 | 1986-03-11 | Chevron Research Company | Lubricant composition containing a mixture of neutralized phosphates |
US5354484A (en) * | 1986-06-13 | 1994-10-11 | The Lubrizol Corporation | Phosphorus-containing lubricant and functional fluid compositions |
US5064546A (en) * | 1987-04-11 | 1991-11-12 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
US4900460A (en) * | 1988-08-02 | 1990-02-13 | Mobil Oil Corp. | Sulfurized olefin adducts of dihydrocarbyl phosphates and phosphites and lubricant compositions containing same |
US5942470A (en) * | 1990-05-17 | 1999-08-24 | Ethyl Petroleum Additives, Inc. | Lubricant compositions |
US5328619A (en) * | 1991-06-21 | 1994-07-12 | Ethyl Petroleum Additives, Inc. | Oil additive concentrates and lubricants of enhanced performance capabilities |
US5358650A (en) * | 1993-04-01 | 1994-10-25 | Ethyl Corporation | Gear oil compositions |
US5571445A (en) * | 1993-04-01 | 1996-11-05 | Ethyl Corporation | Gear oil compositions |
US5547596A (en) * | 1993-05-25 | 1996-08-20 | Idemitsu Kosan Co., Ltd. | Lubricant composition for limited slip differential of car |
US5756429A (en) * | 1993-10-06 | 1998-05-26 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition for high-speed gear |
US5691283A (en) * | 1994-03-01 | 1997-11-25 | Ethyl Petroleum Additives Limited | Use of transmission and gear oil lubricants having enhanced friction properties |
US5500140A (en) * | 1995-03-31 | 1996-03-19 | Ethyl Corporation | Oil-soluble phosphorus- and nitrogen-containing additives |
US5573696A (en) * | 1995-03-31 | 1996-11-12 | Ethyl Corporation | Oil-soluble phosphorus- and nitrogen-containing additives |
US6043200A (en) * | 1995-07-31 | 2000-03-28 | Exxon Chemical Patents, Inc. | Oleaginous compositions |
US5763372A (en) * | 1996-12-13 | 1998-06-09 | Ethyl Corporation | Clean gear boron-free gear additive and method for producing same |
US6046144A (en) * | 1997-06-02 | 2000-04-04 | R.T. Vanderbilt Co., Inc. | Combination of phosphate based additives and sulfonate salts for hydraulic fluids and lubricating compositions |
US5792733A (en) * | 1997-08-14 | 1998-08-11 | The Lubrizol Corporation | Antiwear compositions containing phosphorus compounds and olefins |
US6844300B2 (en) * | 2001-02-20 | 2005-01-18 | Ethyl Corporation | Low phosphorus clean gear formulations |
US20030144157A1 (en) * | 2001-10-23 | 2003-07-31 | Idemitsu Kosan Co., Ltd. | Oil composition for heat treatment of a gear and gear treated by using the oil composition |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106479622A (en) * | 2016-08-26 | 2017-03-08 | 广州吉盛润滑科技有限公司 | A kind of mixing ester type combination of oil for pair of gear worm and its preparation method and application |
Also Published As
Publication number | Publication date |
---|---|
WO2007084208A1 (en) | 2007-07-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1974000B1 (en) | Lubricant composition for a final drive axle | |
JP4873586B2 (en) | High boron formulations for continuously variable transmission fluids | |
AU2006234853B2 (en) | Additive system for lubricants | |
US20060240998A1 (en) | Corrosion protection for lubricants | |
WO2006107435A1 (en) | Fluids for enhanced gear protection | |
KR101571578B1 (en) | Antiwear composition and method of lubricating driveline device | |
JP7369764B2 (en) | Compositions and methods for lubrication of automotive gears, axles, and bearings | |
EP1308496A2 (en) | Tramsmission fluids exhibiting reduced pitting | |
JP2007238944A (en) | Lubricating composition | |
AU2012362446A1 (en) | Limited slip friction modifiers for differentials | |
WO2006107441A1 (en) | Additive system for lubricant | |
US20110111992A1 (en) | Lubricating fluids | |
US20110143982A1 (en) | Additive System for Lubricating Fluids | |
US20070270317A1 (en) | Power Transmission Fluids | |
US20070167334A1 (en) | Lubricating fluids | |
KR20220124257A (en) | Friction modifier compounds and related compositions and methods | |
CA2013698A1 (en) | Lubricant compositions and additives therefor |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: EXXONMOBIL CHEMICAL PATENTS INC., TEXAS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SULLIVAN, WILLIAM;MAHAMAT, HALOU OUMAR;WU, SHI-MING;AND OTHERS;REEL/FRAME:017372/0526 Effective date: 20060322 |
|
AS | Assignment |
Owner name: THE LUBRIZOL CORPORATION,OHIO Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:EXXONMOBIL CHEMICAL PATENTS, INC.;REEL/FRAME:023928/0746 Effective date: 20091201 Owner name: THE LUBRIZOL CORPORATION, OHIO Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:EXXONMOBIL CHEMICAL PATENTS, INC.;REEL/FRAME:023928/0746 Effective date: 20091201 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |