US3595792A - Lubricating oil additives - Google Patents
Lubricating oil additives Download PDFInfo
- Publication number
- US3595792A US3595792A US718930A US3595792DA US3595792A US 3595792 A US3595792 A US 3595792A US 718930 A US718930 A US 718930A US 3595792D A US3595792D A US 3595792DA US 3595792 A US3595792 A US 3595792A
- Authority
- US
- United States
- Prior art keywords
- bismuth
- zinc
- dihydrocarbyl
- additive
- cadmium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000000654 additive Substances 0.000 title abstract description 47
- 239000010687 lubricating oil Substances 0.000 title abstract description 21
- 239000000203 mixture Substances 0.000 abstract description 43
- 239000011701 zinc Substances 0.000 abstract description 31
- 230000000996 additive effect Effects 0.000 abstract description 30
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract description 27
- 229910052725 zinc Inorganic materials 0.000 abstract description 26
- 150000003839 salts Chemical class 0.000 abstract description 18
- 239000003921 oil Substances 0.000 abstract description 17
- 229910052793 cadmium Inorganic materials 0.000 abstract description 15
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract description 15
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 abstract description 10
- 230000001050 lubricating effect Effects 0.000 abstract description 8
- 230000000737 periodic effect Effects 0.000 abstract description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 32
- 229910052797 bismuth Inorganic materials 0.000 description 31
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 25
- 229910000416 bismuth oxide Inorganic materials 0.000 description 14
- 235000014692 zinc oxide Nutrition 0.000 description 14
- 239000002253 acid Substances 0.000 description 13
- TYIXMATWDRGMPF-UHFFFAOYSA-N dibismuth;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Bi+3].[Bi+3] TYIXMATWDRGMPF-UHFFFAOYSA-N 0.000 description 13
- 238000002360 preparation method Methods 0.000 description 12
- 239000011787 zinc oxide Substances 0.000 description 12
- 150000007513 acids Chemical class 0.000 description 11
- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 8
- CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical class [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 description 8
- 230000007935 neutral effect Effects 0.000 description 8
- 150000001621 bismuth Chemical class 0.000 description 7
- 229940049676 bismuth hydroxide Drugs 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000002480 mineral oil Substances 0.000 description 7
- 235000010446 mineral oil Nutrition 0.000 description 7
- TZSXPYWRDWEXHG-UHFFFAOYSA-K bismuth;trihydroxide Chemical compound [OH-].[OH-].[OH-].[Bi+3] TZSXPYWRDWEXHG-UHFFFAOYSA-K 0.000 description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 150000003751 zinc Chemical class 0.000 description 5
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 5
- 229940007718 zinc hydroxide Drugs 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 4
- KSQXYSITBYUVGV-UHFFFAOYSA-K bismuth;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical class [Bi+3].[O-]P([O-])([S-])=S KSQXYSITBYUVGV-UHFFFAOYSA-K 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 231100000241 scar Toxicity 0.000 description 4
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical class [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- -1 alkaline earth metal sulphonate Chemical class 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- PLLZRTNVEXYBNA-UHFFFAOYSA-L cadmium hydroxide Chemical compound [OH-].[OH-].[Cd+2] PLLZRTNVEXYBNA-UHFFFAOYSA-L 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- VBELMRDAQMYTOU-UHFFFAOYSA-N chembl1093419 Chemical compound OC1=CC(O)=CC=C1C(C(=C1)O)=CC2=C1OC1=CC(=O)C(C=3C(=CC(O)=CC=3)O)=CC1=N2 VBELMRDAQMYTOU-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 230000003472 neutralizing effect Effects 0.000 description 3
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- DQNJHGSFNUDORY-UHFFFAOYSA-N bis(2-ethylhexoxy)-sulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCC(CC)COP(S)(=S)OCC(CC)CCCC DQNJHGSFNUDORY-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 2
- FIWYWGLEPWBBQU-UHFFFAOYSA-N 2-heptylphenol Chemical compound CCCCCCCC1=CC=CC=C1O FIWYWGLEPWBBQU-UHFFFAOYSA-N 0.000 description 1
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 240000005020 Acaciella glauca Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
- CHBZNJUDLCHOMC-UHFFFAOYSA-H P(=S)([S-])([O-])[O-].[Cd+2].P(=S)([S-])([O-])[O-].[Cd+2].[Cd+2] Chemical class P(=S)([S-])([O-])[O-].[Cd+2].P(=S)([S-])([O-])[O-].[Cd+2].[Cd+2] CHBZNJUDLCHOMC-UHFFFAOYSA-H 0.000 description 1
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical compound [Cu].[Pb] WIKSRXFQIZQFEH-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 229940036359 bismuth oxide Drugs 0.000 description 1
- 239000011436 cob Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens 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
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 235000003499 redwood Nutrition 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229960001296 zinc oxide Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus 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
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
- C10M137/04—Phosphate esters
- C10M137/10—Thio derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
-
- 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
- C10M2215/086—Imides [having hydrocarbon substituents containing less than thirty carbon atoms]
-
- 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
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- 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
- C10M2223/045—Metal containing thio derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2225/00—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2225/04—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of macromolecualr compounds not containing phosphorus in the monomers
- C10M2225/041—Hydrocarbon polymers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/10—Groups 5 or 15
-
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
- C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
Definitions
- the invention provides a lubricating oil additive consisting essentially of a mixture of at least one bismuth dihydrocarbyl dithiophosphate and at least one salt of a dihydrocarbyl dithiophosphoric acid and a metal of Group III) of the Periodic Table selected from the group consisting of zinc dihydrocarbyl dithiophosphates and cadmium dihydrocarbyl dithiophosphates, which additive may be admixed with an oil of lubricating viscosity, for example in an amount of from 0.01% to 10% by weight based on the total weight of the oil and additive.
- This invention relates to lubricating oil additives and lubricating compositions containing them.
- the metal salts of the diesters of phosphorothiolthionic acids are useful as additives for lubricants.
- the diesters may be prepared by the reaction of alcohols or phenols with phosphorus pentasulphide and then converted into metal salts by direct reaction with a metal oxide or hydroxide.
- salts of a wide variety of metals have been suggested as additives for lubricants and are effective to a greater or less degree, the zinc salts are almost universally preferred on account of their greater oil-solubility and ease of preparation.
- organic zinc dithiophosphates when used as additives for lubricants, are effective inhibitors of oxidation and corrosion of composite metal, e.g. copper-lead, bearings and enhance the load-carrying capacity of the oil. These compounds have the valuable property of reducing wear of valve tappets which sometimes takes place under heavy load.
- a lubricating oil additive comprising a mixture of one or more bismuth dihydrocarbyl dithiophosphates and one or more zinc or cadmium dihydrocarbyl dithiophosphates.
- the invention also provides a lubricating oil additive comprising a mixture of a bismuth dihydrocarbyl dithiophosphate and a zinc dihydrocarbyl dithiophosphate.
- the hydrocarbyl group may be alkyl, alkaryl, aralkyl or aryl which group may be substituted by hydroxyl, halogen or ether groups.
- the hydrocarbyl groups of any acid component of the mixture may be the same or different, and mixtures of acids may be used in the preparation of the additives according to the invention.
- the invention further provides a lubricating composition
- a lubricating composition comprising a major proportion of an oil of lubricating viscosity having admixed therewith a minor proportion of an additive comprising one or more bismuth dihydrocarbyl dithiophosphates and one or more zinc or cadmium dihydrocarbyl dithiophosphates.
- the amount of the bismuth in relation to the total weight of bismuth and zinc and/0r cadmium present in the dihydrocarbyl dithiophosphates will generally be from 5%, preferably 10% to and more preferably from 10 to 60%. In one aspect of the invention the bismuth is present in an amount of 10% to 30% by weight on the total weight of bismuth and zinc and/or cadmium present in the dihydrocarbyl dithiophosphates.
- the additive is a substantially neutral mixed salt of one or more dihydrocarbyl dithiophosphoric acids containing both bismuth and either zinc or cadmium, which may be prepared, for example, by partially neutralising the dithiophosphoric acid or mixture of acids with bismuth oxide or with a mixture of bismuth and zinc or cadmium oxides, the final neutralisation step being achieved by further reacting with zinc or cadmium oxide.
- substantially neutral products can be obtained whereas it is not in general possible to obtain bismuth dithiophosphates free front acidic impurities when using bismuth oxide.
- the invention includes a method of pre paring a lubricating oil additive which method comprises partially neutralising a dihydrocarbyl dithiophosphoric acid or a mixture of dihydrocarbyl dithiophosphoric acids with bismuth oxide or hydroxide or a mixture of bismuth oxide or hydroxide and zinc oxide or hydroxide or cadmium oxide or hydroxide and further reacting the product with zinc oxide or hydroxide or cadmium oxide or hydroxide to provide a substantially neutral, as hereinafter defined, mixture of one or more bismuth dihydrocarbyl dithiophosphates and one or more zinc or cadmium dihydrocarbyl dithiophosphates.
- substantially neutral is meant that either the acidity of the salt, when determined in a solution consisting of 60 volume percent benzene and 40 volume percent neutralised industrial methylated spirit containing 1 ml. of lacmoid indicator per mls. of solvent, is not more than about 1 mg. KOH/g., the solution preferably being neutral or alkaline to the indicator; or that the pH of the salts is greater than 4 and preferably greater than 5, when determined on the pH meter by dissolving 1.5 g. of sample in a mixture of 60 ml. aqueous alcohol (67% alcohol 33% water by volume) and 40 ml. ether.
- the additives of the present invention have improved load carrying properties as compared with the corresponding conventional zinc dialkyl dithiophosphates. They also impart improved oxidation resistance to the oil. In comparison with the corresponding simple bismuth dithiophosphates the substantially neutral mixed salts prepared as hereinbefore described have improved thermal stability in lubricating compositions and show less tendency to promote wear under low loads.
- the dihydrocarbyl dithiophosphoric acid or mixtures thereof may be made by reacting one or more alcohols or phenols or a mixture thereof with phosphorus pentasulphide.
- the mixture of salts may be prepared by making separately one or more bismuth dihydrocarbyl dithiophosphates and one or more dihydrocarbyl dithiophosphates of zinc or cadmium and thereafter mixing the salts together.
- the alcohols which may be used alone or in admixture in preparing the dihydrocarbyl dithiophosphoric acids may be selected from the following:
- the additive so obtained was alkaline to lacmoid indicator and had a pH of 6.5. It had the following analysis:
- the weight ratio of the bismuth and zinc in this mixed salt was therefore approximately 1:1.
- each hydrocarbyl group in the dihydrocarbyl dithiophosphate contains from 3 to 8 carbon atoms.
- the invention also includes mixtures of the additives described above with lubricating oils, either in the form of concentrates or otherwise.
- the invention further includes a lubricating oil composition wherein the amount of additive in the composition is from 0.01 to 10%, preferably from 0.1 to 2.0%, by weight on the weight of the composition.
- the lubricating oil composition according to the invention may also include conventional additives, such as viscosity index improvers, corrosion inhibitors, detergents, dispersants etc.
- the compositions will preferably contain alkaline earth metal sulphonate detergents or barium salts of phosphorsulphurised hydrocarbons such as polyisobutylene, ashless dispersants such as polyisobutenyl succinimides and viscosity index improvers such as long chain alkyl polymethacrylates or polyisobutylene.
- this dithiophosphoric acid (DTPA-Z) (169 g. 0.5 moles) was added to a mineral oil slurry of bismuth and zinc oxides, the reaction being completed by the addition of further zinc oxide as described in Example 1.
- the weights of bismuth and zinc oxide employed were 13.97 g. (0.03 mole) and 14.52 g. (0.178 mole) respectively.
- the product had an acidity of 0.7 mg. KOH/g. and a pH of 5.3. It analysed as follows:
- the product had an acidity of 0.93 mg. KOH/g. and a pH of 4.7. It analysed as follows:
- the product had an acidity of 0.56 mg. KOG/g. and a pH of 4.4. It analysed as follows:
- EXAMPLE 8 Preparation of bismuth salt of DTPA1 This was prepared as described in Example 1 except that all the bismuth oxide (42.7 g. 0.0917 mole) was added at the beginning to the DTPA-l (133 g. 0.5 mole). Twice the normal amount of mineral oil (48 g.) was required to maintain a clear solution.
- the additive had the following analysis:
- the additive was obtained by mixing 20% by weight of the above prepared bismuth salt with 80% by weight of a similarly prepared zinc salt of the same acid.
- the additives of the present invention often show a smaller increase in wear than would be anticipated from the amount of bismuth present.
- Table III which compares the results of tests carried out on blends of several dithiophosphates in mineral oil A, all these blends containing 0.056% phosphorus.
- the 4-ball machine was operated for periods of l-hour under a 15 kg. load, the oil temperature being 50 C. It can be seen from Table III that additives of the present invention gave, under these conditions, wear scar diameters not greatly in excess of the corresponding zinc dithiophosphates, whereas the simple bismuth salts gave substantially increased wear.
- a lubricating oil additive consisting essentially of a mixture of at least one bismuth dihydrocarbyl dithiophosphate and at least one salt selected from the group consisting of zinc dihydrocarbyl dithiophosphates and cadmium dihydrocarbyl dithiophosphates, wherein each hydrocarbyl group contains from 3 to 15 carbon atoms and wherein the amount of bismuth present is from 5% to by weight of the total bismuth and zinc or cadmium present in the dihydrocarbyl dithiophosphates.
- each hydrocarbyl group is an alkyl group containing from 3 to 8 carbon atoms.
- a lubricating oil additive as claimed in claim 1 when prepared by partially neutralising a member of the group consisting of dihydrocarbyl dithiophosphoric acids and mixtures thereof with a member of the group consisting of bismuth oxide, bismuth hydroxide, a mixture of bismuth oxide and zinc oxide, a mixture of bismuth oxide and zinc hydroxide, a mixture of bismuth hydroxide and zinc oxide, a mixture of bismuth hydroxide and zinc hydroxide, a mixture of bismuth oxide and cadmium hydroxide, a mixture of bismuth oxide and cadmium oxide, a mixture of bismuth hydroxide and cadmuim oxide, and a mixture of bismuth hydroxide and cadmium hydroxide and further reacting the partially neutralised product with a member of the group consisting of zinc oxide, zinc hydroxide, cadmium oxide and cadmium hydroxide to provide a substantially neutral mixture of at least one bismuth dihydrocarbyl dithiophosphat
- a lubricating oil additive as claimed in claim 1 consisting essentially of a bismuth dihydrocarbyl dithio phosphate and a zinc dihydrocarbyl dithiophosphate.
- a lubricating oil additive as claimed in claim 5 in admixture with an oil of lubricating viscosity, the additive being admixed with the oil in an amount of from 0.01% to 10% by weight based on the total weight of the oil and additive.
- a lubricating oil additive as claimed in claim 1 in admixture with an oil of lubricating viscosity, the additive being admixed with the oil in an amount of 0.01% to 10% by Weight based on the total weight of the oil and additive.
- a lubricating oil additive as claimed in claim 7 admixed with the oil in an amount of from 01% to 2% by weight.
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Abstract
THE INVENTION PROVIDES A LUBRICATING OIL ADDITIVE CONSISTING ESSENTIALLY OF A MIXTURE OF AT LEAST ONE BISMUTH DIHYDROCARBYL DITHIOPHOSPHATE AND AT LEAST ONE SALT OF A DIHYDROCARBYL DITHIOPHOSPHORIC ACID AND A METAL OF GROUP IIB OF THE PERIODIC TABLE SELECTED FROM THE GROUP CONSISTING OF ZINC DIHYDROCARBYL DITHIOPHOSPHATES AND CADMIUM DIHYDROCARBYL DITHIOPHOSPHATES, WHICH ADDITIVE MAY BE ADMIXED WITH AN OIL OF LUBRICATING VISCOSITY, FOR EXAMPLE IN AN AMOUNT OF FROM 0.01% TO 10% BY WEIGHT BASED ON THE TOTAL WEIGHT OF THE OIL AND ADDITIVE.
Description
United States Patent Ofice 3,595,792 Patented July 27, 1971 3,595,792 LUBRICATING OIL ADDITIVES John Scotchford Elliott and Gerald John Joseph Jayne, London, and Anthony David Brazier, Wokingham, Berkshire, England, assignors to Castrol Limited, London, England No Drawing. Filed Apr. 4, 1968, Ser. N0. 718,930 Claims priority, application Great Britain, Apr. 5, 1967, 15,726/67 Int. Cl. ClOm 1/48 US. Cl. 25232.7 9 Claims ABSTRACT OF THE DISCLOSURE The invention provides a lubricating oil additive consisting essentially of a mixture of at least one bismuth dihydrocarbyl dithiophosphate and at least one salt of a dihydrocarbyl dithiophosphoric acid and a metal of Group III) of the Periodic Table selected from the group consisting of zinc dihydrocarbyl dithiophosphates and cadmium dihydrocarbyl dithiophosphates, which additive may be admixed with an oil of lubricating viscosity, for example in an amount of from 0.01% to 10% by weight based on the total weight of the oil and additive.
This invention relates to lubricating oil additives and lubricating compositions containing them.
It is Well known that the metal salts of the diesters of phosphorothiolthionic acids, generally known as dithiophosphoric acids, are useful as additives for lubricants. The diesters may be prepared by the reaction of alcohols or phenols with phosphorus pentasulphide and then converted into metal salts by direct reaction with a metal oxide or hydroxide.
Though salts of a wide variety of metals have been suggested as additives for lubricants and are effective to a greater or less degree, the zinc salts are almost universally preferred on account of their greater oil-solubility and ease of preparation.
It has been well known for some time that organic zinc dithiophosphates when used as additives for lubricants, are effective inhibitors of oxidation and corrosion of composite metal, e.g. copper-lead, bearings and enhance the load-carrying capacity of the oil. These compounds have the valuable property of reducing wear of valve tappets which sometimes takes place under heavy load.
According to the present invention there is provided a lubricating oil additive comprising a mixture of one or more bismuth dihydrocarbyl dithiophosphates and one or more zinc or cadmium dihydrocarbyl dithiophosphates.
The invention also provides a lubricating oil additive comprising a mixture of a bismuth dihydrocarbyl dithiophosphate and a zinc dihydrocarbyl dithiophosphate. The hydrocarbyl group may be alkyl, alkaryl, aralkyl or aryl which group may be substituted by hydroxyl, halogen or ether groups. The hydrocarbyl groups of any acid component of the mixture may be the same or different, and mixtures of acids may be used in the preparation of the additives according to the invention.
The invention further provides a lubricating composition comprising a major proportion of an oil of lubricating viscosity having admixed therewith a minor proportion of an additive comprising one or more bismuth dihydrocarbyl dithiophosphates and one or more zinc or cadmium dihydrocarbyl dithiophosphates.
The amount of the bismuth in relation to the total weight of bismuth and zinc and/0r cadmium present in the dihydrocarbyl dithiophosphates will generally be from 5%, preferably 10% to and more preferably from 10 to 60%. In one aspect of the invention the bismuth is present in an amount of 10% to 30% by weight on the total weight of bismuth and zinc and/or cadmium present in the dihydrocarbyl dithiophosphates.
In a preferred form of the invention the additive is a substantially neutral mixed salt of one or more dihydrocarbyl dithiophosphoric acids containing both bismuth and either zinc or cadmium, which may be prepared, for example, by partially neutralising the dithiophosphoric acid or mixture of acids with bismuth oxide or with a mixture of bismuth and zinc or cadmium oxides, the final neutralisation step being achieved by further reacting with zinc or cadmium oxide. In this manner substantially neutral products can be obtained whereas it is not in general possible to obtain bismuth dithiophosphates free front acidic impurities when using bismuth oxide.
Accordingly the invention includes a method of pre paring a lubricating oil additive which method comprises partially neutralising a dihydrocarbyl dithiophosphoric acid or a mixture of dihydrocarbyl dithiophosphoric acids with bismuth oxide or hydroxide or a mixture of bismuth oxide or hydroxide and zinc oxide or hydroxide or cadmium oxide or hydroxide and further reacting the product with zinc oxide or hydroxide or cadmium oxide or hydroxide to provide a substantially neutral, as hereinafter defined, mixture of one or more bismuth dihydrocarbyl dithiophosphates and one or more zinc or cadmium dihydrocarbyl dithiophosphates.
By substantially neutral" is meant that either the acidity of the salt, when determined in a solution consisting of 60 volume percent benzene and 40 volume percent neutralised industrial methylated spirit containing 1 ml. of lacmoid indicator per mls. of solvent, is not more than about 1 mg. KOH/g., the solution preferably being neutral or alkaline to the indicator; or that the pH of the salts is greater than 4 and preferably greater than 5, when determined on the pH meter by dissolving 1.5 g. of sample in a mixture of 60 ml. aqueous alcohol (67% alcohol 33% water by volume) and 40 ml. ether.
The additives of the present invention have improved load carrying properties as compared with the corresponding conventional zinc dialkyl dithiophosphates. They also impart improved oxidation resistance to the oil. In comparison with the corresponding simple bismuth dithiophosphates the substantially neutral mixed salts prepared as hereinbefore described have improved thermal stability in lubricating compositions and show less tendency to promote wear under low loads.
The dihydrocarbyl dithiophosphoric acid or mixtures thereof may be made by reacting one or more alcohols or phenols or a mixture thereof with phosphorus pentasulphide.
In a further aspect of the invention the mixture of salts may be prepared by making separately one or more bismuth dihydrocarbyl dithiophosphates and one or more dihydrocarbyl dithiophosphates of zinc or cadmium and thereafter mixing the salts together. The alcohols which may be used alone or in admixture in preparing the dihydrocarbyl dithiophosphoric acids may be selected from the following:
4 hour. The product was then vacuum stripped at 80 C. at about 10 mm. pressure to remove excess alcohols.
The additive so obtained was alkaline to lacmoid indicator and had a pH of 6.5. It had the following analysis:
131.68% (calc. 6.56%) Zn, 6.01% (calc. 6.35%) P, 8.94% (calc. 8.96%)
The weight ratio of the bismuth and zinc in this mixed salt was therefore approximately 1:1.
Further examples of the preparation of compounds according to the present invention are given in Table l, the same dithiophosphoric acid being used as in Example 1 and the method of preparation being substantially the same in each case. The only difference was in the ratio of bismuth oxide to zinc oxide employed. All these products were alkaline to lacmoid indicator and had pl-Is in the range 6.16.6.
TABLE I.BIS.\1UTII 'ZINC DITIIIOPHOSPIIATES FROM DTPAJ ZnO B1903 Percent Bl Percent Zn Weight ratio, Example No. Wt. tg.) Moles Wt. (g) Moles Found Calcd Found Calc'd BizZn The phenols may be alkylated phenols, particularly P- EXAMPLE 5 octyl phenol, p-nonyl phenol and heptyl phenol. The mixture of salts according to this invention may be formed from any of the acids or mixtures of acids described in British patent specification No. 822,655. In one aspect of the invention each hydrocarbyl group in the dihydrocarbyl dithiophosphate contains from 3 to 8 carbon atoms.
The invention also includes mixtures of the additives described above with lubricating oils, either in the form of concentrates or otherwise.
The invention further includes a lubricating oil composition wherein the amount of additive in the composition is from 0.01 to 10%, preferably from 0.1 to 2.0%, by weight on the weight of the composition.
The lubricating oil composition according to the invention may also include conventional additives, such as viscosity index improvers, corrosion inhibitors, detergents, dispersants etc. The compositions will preferably contain alkaline earth metal sulphonate detergents or barium salts of phosphorsulphurised hydrocarbons such as polyisobutylene, ashless dispersants such as polyisobutenyl succinimides and viscosity index improvers such as long chain alkyl polymethacrylates or polyisobutylene.
The preparation of additives according to the present invention will now be illustrated with reference to the following examples.
EXAMPLE 1 Preparation of bismuth/zinc (1:1) salt of DTPA-1 The dithiophosphoric acid (133 g. 0.5 mole) was run in a slowly from the tap funnel at such a rate as to maintain the temperature at about C. (about 30 minutes). The remainder of the zinc oxide was then added, the total amount of zinc oxide added being 14.52 g. (0.178 mole) and the mixture was then stirred at 60 C. for a further Preparation of bismuth/zinc (1:1) salt of DTPA-2 A mixture of dialkyl dithiophosphoric acids was prepared from isopropanol (199 g., 3.32 moles), capryl alcohol (600 g., 4.62 moles) and phosphorous pentasulphide (378 g. 17 moles) in the manner described in Example 1, but at a temperature of C.
Employing essentially the same method as described in Example 1 this dithiophosphoric acid (DTPA-Z) (169 g. 0.5 moles) was added to a mineral oil slurry of bismuth and zinc oxides, the reaction being completed by the addition of further zinc oxide as described in Example 1. The weights of bismuth and zinc oxide employed were 13.97 g. (0.03 mole) and 14.52 g. (0.178 mole) respectively. The product had an acidity of 0.7 mg. KOH/g. and a pH of 5.3. It analysed as follows:
Bi, 6.4% (calc. 6.2%) Zn. 4.9% (calc. 6.4%) P, 7.44% (calc. 7.8%)
EXAMPLE 6 Preparation of bismuth/zinc (1 :1) salt of di-(2- ethyl hexyl) dithiophosphoric acid Employing essentially the same method as described in Example 1, di-Z-ethylhexyl dithiophosphoric acid (111 g. 0.2 mole), prepared from Z-ethyl hexanol (1040 g. 8.0 moles) and phosphorus pentasulphide (444 g. 2.0 moles) at 8090 C. was added to a mineral oil slurry of bismuth oxide and zinc oxide, the weights of bismuth and Zinc oxides employed being 8.4 g. (0.018 mole) and 8.75 g. (0.107 mole) respectively.
The product had an acidity of 0.93 mg. KOH/g. and a pH of 4.7. It analysed as follows:
Bi, 4.3% (calc. 5.15%) Zn, 4.8% (calc. 4.95%) P, 6.75% (calc. 6.45%)
EXAMPLE 7 Preparation of bismuth/cadmium (1:1) salt of di(2- ethyl hexyl) dithiophosphoric acid I Employing essentially the same method as described m Example 1, di-Z-ethylhexyl dithiophosphoric acid (114.3 g.0.3 mole), from a subsequent preparation similar to that in Example 6, was added to a mineral oil slurry of bismuth oxide and cadmium oxide, the weights of the bismuth and cadmium oxides being 11.6 g. (0.025 mole) and 11.3 g. (0.09 mole) respectively.
The product had an acidity of 0.56 mg. KOG/g. and a pH of 4.4. It analysed as follows:
Bi, 5.6% (calc. 6.6%) Cd, 7.3% (calc. 6.6%) P, 6.46% (calc. 6.1%)
EXAMPLE 8 Preparation of bismuth salt of DTPA1 This was prepared as described in Example 1 except that all the bismuth oxide (42.7 g. 0.0917 mole) was added at the beginning to the DTPA-l (133 g. 0.5 mole). Twice the normal amount of mineral oil (48 g.) was required to maintain a clear solution. The additive had the following analysis:
Bi, 15.0% (calc. 14.7%) P, 6.59% (calc. 6.64%)
The additive was obtained by mixing 20% by weight of the above prepared bismuth salt with 80% by weight of a similarly prepared zinc salt of the same acid.
In order to demonstrate the antioxidant properties of the additives of the present invention in a typical lubricating oil, blends were prepared in mineral oil A, which was a solvent refined mineral oil of viscosity approximately 160 seconds Redwood 1 at 140 F. These blends were all made up to contain 0.072% phosphorus and comparison was made with certain conventional zinc dialkyl dithiophosphates and with bismuth dialkyl dithiophosphates which did not contain zinc or cadmium. These oils were subjected to the well-known Rotary Bomb test, a description of which is given in British patent specification No. 1,023,380 on page 12 lines -22. The results of these tests and the conditions employed are given on Table II. The advantage of the additives of the present invention over the corresponding zinc or cadmium dithiophosphates is clearly seen from this table and in some cases the additives of the present invention also show an advantage over the simple bismuth salts.
When the load carrying properties of the additives of the present invention are compared with those of the corresponding zinc dithiophosphates on the 4-ball machine at room temperature by the standard procedure employ ing a series of l-minute runs at different loads, a distinct improvement in load carrying capacity is consistently obtained as judged by a comparison of the wear scar diameters at loads above the point of incipient seizure. In general it has been found that the higher the amount of bismuth dithiophosphate in the oil the smaller the wear scar diameter. When, however, wear tests are carried out on the 4-ball machine at low loads the amount of wear given by the bismuth dithiophosphates is significantly greater than that given by the corresponding zinc dithiophosphates. The additives of the present invention, particularly the substantially neutral products obtained by the preferred method of preparation, often show a smaller increase in wear than would be anticipated from the amount of bismuth present. This is illustrated in Table III, which compares the results of tests carried out on blends of several dithiophosphates in mineral oil A, all these blends containing 0.056% phosphorus. The 4-ball machine was operated for periods of l-hour under a 15 kg. load, the oil temperature being 50 C. It can be seen from Table III that additives of the present invention gave, under these conditions, wear scar diameters not greatly in excess of the corresponding zinc dithiophosphates, whereas the simple bismuth salts gave substantially increased wear.
TABLE II.-ROTARY BOMB TEST Temperature 150 C. 3 metres of copper wire Initial pressure .10 p.s.i.
Induction period Additive Percent (minutes) None 20 Zinc salt of D'IPA-i.. 0.75 233 Bismuth salt at DIPA-l 1.08 275 Product of Example:
Zinc salt of UTPA 0. 98 100 Bismuth salt of DTPA 0. 975 240 Product of Example 5- 0. U? 237 Cadmium di (Z-ethyl huxyl) dithiophosphate. 1.22 280 Bismuth di (Bethyl liexyl) ditliiophosphato 1. i7 271 Product of Example 7 1.11 300 TABLE III.4BALL WEAR TESTS (i5 kg.1 hr. -50 C.)
Precent inc.
Mean wear in wear over scar diam. zinc com- Additive Percent tmm.) pound Zinc salt of DTPA-i 0. 58 0. 206
Bismuth salt of DIPA-l 0. S4 0. 433 46 Product of Example:
0. 286 Nil phosphate 0. 915 0. 400 35 Product of Example 6 0. 83 0. 312 6 We claim:
1. A lubricating oil additive consisting essentially of a mixture of at least one bismuth dihydrocarbyl dithiophosphate and at least one salt selected from the group consisting of zinc dihydrocarbyl dithiophosphates and cadmium dihydrocarbyl dithiophosphates, wherein each hydrocarbyl group contains from 3 to 15 carbon atoms and wherein the amount of bismuth present is from 5% to by weight of the total bismuth and zinc or cadmium present in the dihydrocarbyl dithiophosphates.
2. A lubricating oil additive as claimed in claim 1 wherein each hydrocarbyl group is an alkyl group containing from 3 to 8 carbon atoms.
3. A lubricating oil additive as claimed in claim 1 wherein the amount of bismuth present is from 10% to 60%.
4. A lubricating oil additive as claimed in claim 1 when prepared by partially neutralising a member of the group consisting of dihydrocarbyl dithiophosphoric acids and mixtures thereof with a member of the group consisting of bismuth oxide, bismuth hydroxide, a mixture of bismuth oxide and zinc oxide, a mixture of bismuth oxide and zinc hydroxide, a mixture of bismuth hydroxide and zinc oxide, a mixture of bismuth hydroxide and zinc hydroxide, a mixture of bismuth oxide and cadmium hydroxide, a mixture of bismuth oxide and cadmium oxide, a mixture of bismuth hydroxide and cadmuim oxide, and a mixture of bismuth hydroxide and cadmium hydroxide and further reacting the partially neutralised product with a member of the group consisting of zinc oxide, zinc hydroxide, cadmium oxide and cadmium hydroxide to provide a substantially neutral mixture of at least one bismuth dihydrocarbyl dithiophosphate and at least one member of the group consisting of zinc dihydrocarbyl dithiophosphates and cadmium dihydrocarbyl dithiophosphates.
5. A lubricating oil additive as claimed in claim 1 consisting essentially of a bismuth dihydrocarbyl dithio phosphate and a zinc dihydrocarbyl dithiophosphate.
6. A lubricating oil additive as claimed in claim 5 wherein the amount of bismuth present is from 10% to 90% by weight of the total weight of bismuth and zinc present in the dihydrocarbyl dithiophosphate.
7. A lubricating oil additive as claimed in claim 5 in admixture with an oil of lubricating viscosity, the additive being admixed with the oil in an amount of from 0.01% to 10% by weight based on the total weight of the oil and additive.
8. A lubricating oil additive as claimed in claim 1 in admixture with an oil of lubricating viscosity, the additive being admixed with the oil in an amount of 0.01% to 10% by Weight based on the total weight of the oil and additive.
9. A lubricating oil additive as claimed in claim 7 admixed with the oil in an amount of from 01% to 2% by weight.
References Cited DANIEL E. WYMAN, Primary Examiner 10 I. VAUGHN, Assistant Examiner US. Cl. X.R. 252400
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB05726/67A GB1163025A (en) | 1967-04-05 | 1967-04-05 | Lubricating Oil Additives and Lubricating Compositions containing them |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3595792A true US3595792A (en) | 1971-07-27 |
Family
ID=10064399
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US718930A Expired - Lifetime US3595792A (en) | 1967-04-05 | 1968-04-04 | Lubricating oil additives |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3595792A (en) |
| JP (1) | JPS4819681B1 (en) |
| DE (1) | DE1769115B1 (en) |
| FR (1) | FR1575670A (en) |
| GB (1) | GB1163025A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4116871A (en) * | 1977-06-29 | 1978-09-26 | Chevron Research Company | Preparation of phosphorus-containing acids and salts |
| US5015402A (en) * | 1986-11-07 | 1991-05-14 | The Lubrizol Corporation | Basic metal dihydrocarbylphosphorodithioates |
| US5576273A (en) * | 1995-11-20 | 1996-11-19 | R.T. Vanderbilt Company, Inc. | Lubricating compositions containing bismuth compounds |
| US5739089A (en) * | 1987-11-24 | 1998-04-14 | Exxon Chemical Patents Inc. | Dihydrocarbyl dithiophosphates |
| CN114686289A (en) * | 2022-03-03 | 2022-07-01 | 新乡市瑞丰新材料股份有限公司 | Hydraulic oil additive with excellent performance and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5178782A (en) * | 1985-03-12 | 1993-01-12 | The Lubrizol Corporation | Metal salts of mixed aromatic/aliphatic phosphorodithioic acids |
-
1967
- 1967-04-05 GB GB05726/67A patent/GB1163025A/en not_active Expired
-
1968
- 1968-04-04 US US718930A patent/US3595792A/en not_active Expired - Lifetime
- 1968-04-04 FR FR1575670D patent/FR1575670A/fr not_active Expired
- 1968-04-05 JP JP43022364A patent/JPS4819681B1/ja active Pending
- 1968-04-05 DE DE19681769115 patent/DE1769115B1/en active Pending
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4116871A (en) * | 1977-06-29 | 1978-09-26 | Chevron Research Company | Preparation of phosphorus-containing acids and salts |
| US5015402A (en) * | 1986-11-07 | 1991-05-14 | The Lubrizol Corporation | Basic metal dihydrocarbylphosphorodithioates |
| US5739089A (en) * | 1987-11-24 | 1998-04-14 | Exxon Chemical Patents Inc. | Dihydrocarbyl dithiophosphates |
| US5576273A (en) * | 1995-11-20 | 1996-11-19 | R.T. Vanderbilt Company, Inc. | Lubricating compositions containing bismuth compounds |
| CN114686289A (en) * | 2022-03-03 | 2022-07-01 | 新乡市瑞丰新材料股份有限公司 | Hydraulic oil additive with excellent performance and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS4819681B1 (en) | 1973-06-15 |
| DE1769115B1 (en) | 1971-05-06 |
| FR1575670A (en) | 1969-07-25 |
| GB1163025A (en) | 1969-09-04 |
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