EP0578435A1 - Friction modification of synthetic gear oils - Google Patents

Friction modification of synthetic gear oils Download PDF

Info

Publication number
EP0578435A1
EP0578435A1 EP19930305125 EP93305125A EP0578435A1 EP 0578435 A1 EP0578435 A1 EP 0578435A1 EP 19930305125 EP19930305125 EP 19930305125 EP 93305125 A EP93305125 A EP 93305125A EP 0578435 A1 EP0578435 A1 EP 0578435A1
Authority
EP
European Patent Office
Prior art keywords
oil
lubricant
gear
parts
additive
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.)
Granted
Application number
EP19930305125
Other languages
German (de)
French (fr)
Other versions
EP0578435B1 (en
Inventor
Ian Macpherson
Donald Gale Campbell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Afton Chemical Ltd
Original Assignee
Afton Chemical Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=25429898&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0578435(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Afton Chemical Ltd filed Critical Afton Chemical Ltd
Publication of EP0578435A1 publication Critical patent/EP0578435A1/en
Application granted granted Critical
Publication of EP0578435B1 publication Critical patent/EP0578435B1/en
Anticipated expiration legal-status Critical
Revoked legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • C10M169/044Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/36Esters of polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/38Esters of polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/42Complex esters, i.e. compounds containing at least three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compound: monohydroxy compounds, polyhydroxy compounds, monocarboxylic acids, polycarboxylic acids and hydroxy carboxylic acids
    • C10M105/44Complex esters, i.e. compounds containing at least three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compound: monohydroxy compounds, polyhydroxy compounds, monocarboxylic acids, polycarboxylic acids and hydroxy carboxylic acids derived from the combination of monocarboxylic acids, dicarboxylic acids and dihydroxy compounds only and having no free hydroxy or carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/02Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
    • C10M107/10Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation containing aliphatic monomer having more than 4 carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/04Hydroxy compounds
    • C10M129/10Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/26Carboxylic acids; Salts thereof
    • C10M129/28Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M129/38Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
    • C10M129/40Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms monocarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/26Carboxylic acids; Salts thereof
    • C10M129/28Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M129/38Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
    • C10M129/42Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms polycarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/04Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M133/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/38Heterocyclic nitrogen compounds
    • C10M133/44Five-membered ring containing nitrogen and carbon only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/52Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
    • C10M133/56Amides; Imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M135/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/02Sulfurised compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M135/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/08Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium containing a sulfur-to-oxygen bond
    • C10M135/10Sulfonic acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M135/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/20Thiols; Sulfides; Polysulfides
    • C10M135/22Thiols; Sulfides; Polysulfides containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M135/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/32Heterocyclic sulfur, selenium or tellurium compounds
    • C10M135/36Heterocyclic sulfur, selenium or tellurium compounds the ring containing sulfur and carbon with nitrogen or oxygen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • C10M137/08Ammonium or amine salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • C10M137/10Thio derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M143/00Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
    • C10M143/04Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing propene
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/10Macromolecular 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
    • C10M145/12Macromolecular 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 monocarboxylic
    • C10M145/14Acrylate; Methacrylate
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/18Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/24Polyethers
    • C10M145/26Polyoxyalkylenes
    • C10M145/34Polyoxyalkylenes of two or more specified different types
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/18Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/24Polyethers
    • C10M145/26Polyoxyalkylenes
    • C10M145/38Polyoxyalkylenes esterified
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M159/00Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12Reaction products
    • C10M159/123Reaction products obtained by phosphorus or phosphorus-containing compounds, e.g. P x S x with organic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M159/00Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12Reaction products
    • C10M159/16Reaction products obtained by Mannich reactions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M159/00Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12Reaction products
    • C10M159/20Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
    • C10M159/24Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing sulfonic radicals
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • C10M169/048Mixtures of base-materials and additives the additives being a mixture of compounds of unknown or incompletely defined constitution, non-macromolecular and macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/024Propene
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
    • C10M2205/0285Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/026Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027Neutral salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/126Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/127Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids polycarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/22Acids obtained from polymerised unsaturated acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
    • C10M2207/2825Esters of (cyclo)aliphatic oolycarboxylic acids used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • C10M2207/2835Esters of polyhydroxy compounds used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/285Esters of aromatic polycarboxylic acids
    • C10M2207/2855Esters of aromatic polycarboxylic acids used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/286Esters of polymerised unsaturated acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/30Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
    • C10M2207/302Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids derived from the combination of monocarboxylic acids, dicarboxylic acids and dihydroxy compounds only and having no free hydroxy or carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/30Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
    • C10M2207/302Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids derived from the combination of monocarboxylic acids, dicarboxylic acids and dihydroxy compounds only and having no free hydroxy or carboxyl groups
    • C10M2207/3025Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids derived from the combination of monocarboxylic acids, dicarboxylic acids and dihydroxy compounds only and having no free hydroxy or carboxyl groups used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular 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
    • C10M2209/084Acrylate; Methacrylate
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/107Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/109Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/08Amides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/08Amides
    • C10M2215/082Amides containing hydroxyl groups; Alkoxylated derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/086Imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/221Six-membered rings containing nitrogen and carbon only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/223Five-membered rings containing nitrogen and carbon only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C10M2215/226Morpholines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/28Amides; Imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/30Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/043Mannich bases
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/046Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/06Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/02Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/02Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
    • C10M2219/022Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of hydrocarbons, e.g. olefines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046Overbasedsulfonic acid salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/083Dibenzyl sulfide
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/102Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon only in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/106Thiadiazoles
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/108Phenothiazine
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/041Triaryl phosphates
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/042Metal salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/043Ammonium or amine salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/045Metal containing thio derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/047Thioderivatives not containing metallic elements
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/049Phosphite
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/10Phosphatides, e.g. lecithin, cephalin
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/12Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/12Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy
    • C10M2223/121Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy of alcohols or phenols
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/06Organic compounds derived from inorganic acids or metal salts
    • C10M2227/061Esters derived from boron
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2070/00Specific manufacturing methods for lubricant compositions
    • C10N2070/02Concentrating of additives

Definitions

  • This invention relates to improving the frictional characteristics of gear oils in which the base oil is, or contains a significant quantity of, a synthetic oil such as a polyalpha-olefin oil (PAO) or a synthetic ester oil.
  • a synthetic oil such as a polyalpha-olefin oil (PAO) or a synthetic ester oil.
  • Modern commercial large vehicles equipped with manual transmissions of the synchronizer type are typically operated with conventional mineral oil-based transmission lubricants.
  • Such lubricants contain additives for wear protection, corrosion protection, and other beneficial property improvements.
  • the level and type of additive used depends on the performance requirements of the oil, including low temperature properties, or wear protection.
  • Performance designations which are used include API-GL4 and API-GL5. More recently PG1, PG2 and API-GL7 are being defined. Additionally a degree of demulsification may be preferred.
  • API-GL4 and lower performance specifications may be met using conventional crankcase mineral oil lubricants containing conventional levels of zinc dialkydithiophosphates, sulfonates, or ashless dispersants.
  • P/S essentially ashless formulations, although up to at least API-GL5 has been met by P/S formulations containing significant levels of alkali metal borates and metal sulfonates (e.g., OLOA 9750 additive).
  • P/S refers to gear oil additive packages in which a phosphorus and sulfur-containing antiwear and/or extreme pressure additive system is employed.
  • the additives used pursuant to this invention are alkali or alkaline earth metal salts of oil-soluble sulfonic acids, such as petroleum sulfonic acids, preferably alkylaryl sulfonic acids and, more preferably, alkylbenzene sulfonic acids.
  • the metals of such salts preferably are those which have low toxicity and which present little or no concern from the environmental standpoint, namely, lithium, sodium, potassium, magnesium, and calcium.
  • barium and strontium sulfonates can be used, if desired.
  • API-GL5 gear oil compositions used in actual practice that apparently contain a metal sulfonate component.
  • SPIRAX MB 90 trademark of the Shell Oil Companies
  • barium believed to be in the form of a barium sulfonate corrosion inhibitor.
  • the other type is based on use of gear oil additive packages containing high levels of potassium borate dispersion serving as an antiwear/extreme pressure agent. These packages are believed to contain low levels of calcium, presumably in the form of a sulfonate. These packages are apparently used primarily (if not exclusively) in conventional mineral oil stocks in forming finished gear oils. And in any event, the levels of the potassium borate used in the finished oils (e.g., 1-2 wt%) are sufficiently high as to seriously impair the results obtainable by the practice of this invention and thus are outside of the permissible concentrations of this invention.
  • a gear oil lubricant having a kinematic viscosity at 100° C in the range of 4 to 32 mm2.s ⁇ 1 (cSt), and preferably in the range of 8 to 20 mm2.s ⁇ 1 (cSt), and comprising:
  • finished gear lubricants of this invention manifests itself in a substantial increase in the number of cycles during which the test can be performed without poor synchronization of the gear changes.
  • a finished synthetic oil-based gear oil devoid of a metal sulfonate additive may encounter substantial failure within 10,000 or 15,000 cycles.
  • finished synthetic oil-based lubricants of this invention which contain a metal sulfonate component can achieve at least 50,000 and usually at least 100,000 cycles of trouble free operation in this test procedure.
  • the gear oil additive package used as component b) may in fact satisfy the requirements for other performance specifications such as API-GL5, and including specifications not yet in being (or even envisioned) such as PG1, PG2 and API-GL7 or specifications of other countries such as comparable JIS gear oil standards, or the like.
  • the specifications of API-GL4 are to be considered minimum performance levels for the package.
  • API-GL7 For example, if the requirements of the API-GL7 specification are more stringent for the most part than, say, API-GL4, the fact that an additive package satisfies the API-GL7 requirements inherently satisfies the minimum performance requirements for use in the practice of this invention, whether or not the package has actually been subjected to the API-GL4 performance tests.
  • a gear oil additive package which comprises (1) an oil-soluble phosphorus and sulfur-containing antiwear and/or extreme pressure additive complement and (2) at least one alkali or alkaline earth metal salt of an oil-soluble sulfonic acid; said gear oil additive package being further characterized in that when blended with a base oil having a kinematic viscosity in the range of 4 to 32 cSt at 100°C and composed of at least 25% by volume of (i) hydrogenated poly-alpha-olefin oligomer oil or (ii) synthetic ester oil, or (iii) a combination of (i) and (ii) to form a lubricant containing from 0.01 to 2 wt % of said metal salt, said gear oil additive package provides a lubricant composition that:
  • Still another aspect of this invention is the method of beneficially modifying the frictional characteristics of a low-friction synthetic lubricant composition containing a gear oil additive package such that the lubricant composition satisfies or exceeds the specifications for API-GL4 service, but does not exhibit satisfactory friction properties for use in manual transmissions, particularly those of the synchronizer type.
  • the method comprises including in such lubricant composition an amount in the range of 0.01 to 2 wt % based on the total weight of the lubricant of at least one metal salt of an oil-soluble sulfonic acid such that the friction properties of said lubricant are improved for use in manual transmissions, particularly those of the syn-chronizer type.
  • the metal of the sulfonate salt preferably is lithium, sodium, potassium, magnesium, or calcium, or a combination of two or more such metals.
  • barium and/or strontium sulfonates can be used if desired.
  • the metal sulfonate can be employed as a separate component (e.g., as a "top-treat" to the base oil with which the additive package has been or will be blended) or as a component of the additive package itself.
  • a separate component e.g., as a "top-treat" to the base oil with which the additive package has been or will be blended
  • a component of the additive package itself e.g., as a "top-treat" to the base oil with which the additive package has been or will be blended
  • additive packages it is possible to blend the metal sulfonate and the respective components of the additive package into the base oil individually or in various compatible sub-combinations.
  • the base oils are composed partially or entirely of a low-friction fluid such as PAO base oil and/or a synthetic ester lubricating oil.
  • the PAO fluids are usually formed by oligomerization or co-oligomerization of 1-alkene hydrocarbon having 6 to 20 and preferably 8 to 16 carbon atoms in the molecule and hydrogenation of the resultant oligomer. Hydrogenated oligomers formed from 1-decene are particularly preferred. Methods for the production of such liquid oligomeric 1-alkene hydrocarbons are known and reported in the literature. See for example U. S. Pat. Nos. 3,763,244; 3,780,128; 4,172,855; 4,218,330; and 4,950,822. Additionally, suitable hydrogenated 1-alkene oligomers of this type are available as articles of commerce, for example, from Ethyl Corporation and its affiliates under the trade mark ETHYLFLO.
  • Synthetic ester oils are also well known and widely available in the marketplace.
  • Typical synthetic ester oils include such materials as the esters of dicarboxylic acids (e.g., phthalic acid, succinic acid, maleic acid, azelaic acid, suberic acid, sebacic acid, fumaric acid, adipic acid, linoleic acid dimer) with a variety of alcohols (e.g., butyl alcohol, hexyl alcohol, dodecyl alcohol, 2-ethylhexyl alcohol, ethylene glycol).
  • dicarboxylic acids e.g., phthalic acid, succinic acid, maleic acid, azelaic acid, suberic acid, sebacic acid, fumaric acid, adipic acid, linoleic acid dimer
  • alcohols e.g., butyl alcohol, hexyl alcohol, dodecyl alcohol, 2-ethylhexyl alcohol, ethylene glycol
  • esters include dibutyl adipate, di(1-ethylpropyl) adipate, di(1,3-dimethylbutyl) adipate, di(2-ethylhexyl) adipate, didodecyl adipate, di(tridecyl) adipate, di(2-ethylhexyl) sebacate, dilauryl sebacate, di-n-hexylfumarate, dioctyl sebacate, di(1-methylpropyl) azelate, diisooctyl azelate, diisodecyl azelate, dioctyl phthalate, didecyl phthalate, mixed C9 and C11 dialkyl phthalate, dibutyl sebacate, di(1-ethylpropyl) sebacate, di(eicosyl) sebacate, the 2-ethylhexyl
  • synthetic esters which may be used as synthetic oils include those made from C3-C12 monocarboxylic acids and polyols and polyol ethers such as neopentyl glycol, trimethylolpropane, pentaerythritol and dipentaerythritol. Trimethylol propane tripelargonate and pentaerythritol tetracaproate serve as examples.
  • Suitable commercially available products include Emkarate 911P (ICI, plc.), and KETJENLUBE synthetic oil (Akzo Chemicals).
  • the base oils may contain up to 75%, preferably no more than 50%, and more preferably no more than 25% by weight of a mineral oil or other suitable oleaginous liquid of lubricating viscosity, provided the overall base lubricant is suitable for use in forming a finished gear lubricant that satisfies or exceeds the specifications for API-GL4 service, and provided further that the resultant finished oil remains amenable to friction improvement pursuant to this invention. It will be understood that most gear oil packages contain diluent oils or solvents for certain active ingredients or components.
  • the finished gear oil lubricant may contain up to 75% by weight of a mineral oil or the like, plus an additional amount of diluent oil or solvent emanating from the additives or additive package used in formulating the finished lubricant.
  • the metal sulfonates used in the invention are preferably overbased metal sulfonates, but the so-called neutral metal sulfonates can be used, if desired.
  • Petroleum sulfonates are usually prepared by the sulfonation of suitable petroleum fractions with subsequent removal of acid sludge and purification followed by neutralization with the appropriate basic metal compound (e.g., oxide or hydroxide). Petroleum oxidates such as described in EP Pub. No. 275,395 (published July 27, 1988) can be used in forming overbased sulfonates.
  • Alkylaryl sulfonates are usually prepared by sulfonation of alkylated benzene or benzene analogs (toluene, naphthalene, phenothiazine, diphenyl oxide, or diphenyl sulfide), followed by workup and neutralization.
  • alkylbenzenes suitable for producing the sulfonates can be formed by alkylating benzene with an oligomer or polymer such as tetrapropylene in the presence of an Friedel-Crafts catalyst.
  • oligomer or polymer such as tetrapropylene
  • Friedel-Crafts catalyst a number of highly suitable metal sulfonates are available as articles of commerce.
  • Quantities ranging from as little as 0.01 % wt % up to as much as 2 % by wt % or more of the metal sulfonate based on the total weight of the finished lubricant can be employed. Ordinarily the amount used will not be greatly in excess of that amount needed to yield the friction performance desired in the particular finished gear oil lubricant in question. Thus often the amount will not be above 1 wt %, and in some cases will not exceed 0.5 wt %.
  • the amount will be proportioned such that when the package is blended into the base oil at the recommended or desired concentration, the resultant finished oil will contain from 0.01 wt % up to 2 wt % or more, preferably up to about 1 wt %, and in some cases up to about 0.5 wt % of the metal sulfonate. It is to be noted that these proportions of the metal sulfonate are based on the active ingredient, and thus the weight of any solvent or diluent associated with the metal sulfonate as used should be subtracted from the additive weight when calculating the concentration of metal sulfonate in the finished oil or in the friction-improved additive package. However the total weight of the finished oil or of the completed additive package will include the weight of such solvent or diluent.
  • API-GL4 and API-GL5 service are published in ASTM Publication STP-512A entitled “Laboratory Performance Tests for Automotive Gear Lubricants” (March 1987).
  • a number of gear oil additive packages that provide API-GL4 or API-GL5 performance are available in the marketplace. They generally contain at least a sulfur-phosphorus antiwear or extreme pressure additive system, one or more antioxidants, one or more corrosion inhibitors, and an antifoam additive, and may, and preferably do, contain a dispersant additive.
  • a gear oil additive package which comprises:
  • a finished lubricant composition containing at least the foregoing components a), b), c) and d) constitutes still another embodiment of this invention.
  • Such finished lubricant satisfies or exceeds the specifications for API-GL4 service, and preferably satisfies or exceeds the specifications for API-GL5 service.
  • Component a) of the foregoing additive package and finished lubricant composition most preferably is a Mannich base which includes or, alternatively, consists of boronated Mannich base ashless dispersant.
  • Yet another embodiment of this invention involves using as component a) a Mannich base dispersant and proportioning components a) and b) above in the additive package or in the finished lubricant composition such that the mass ratio (wt/wt) of nitrogen in the Mannich base dispersant to sulphur in the sulphur-containing antiwear and/or extreme pressure agent is in the range of 0.0005:1 to 0.5:1, and preferably in the range of 0.003:1 to 0.2:1.
  • a Mannich base dispersant is employed as component a) and components a) and c) above are proportioned in the additive package or in the finished lubricant such that the mass ratio (wt/wt) of nitrogen in the Mannich base dispersant to phosphorus in the metal-free phosphorus-containing antiwear and/or extreme pressure agent is in the range of 0.005:1 to 5:1, and preferably in the range of 0.01:1 to 2:1.
  • any of the above additive concentrates and finished lubricant compositions further comprise at least one oil-soluble demulsifying agent.
  • any of the above additive concentrates and finished lubricant compositions further comprise at least one oil-soluble amine salt of a sulphur-free hydrocarbyl phosphoric acid.
  • the lubricant compositions of this invention have a halogen content, if any, of no more than 100 ppm, and more preferably no more than 30 ppm on a weight basis.
  • the ZF.Synchronizer test has been designed for the evaluation of oil performance in commercially available synchromesh units under endurance conditions with the bulk lubricant temperature controlled at a relatively high level. While it is important to simulate fairly closely the actual conditions met in service, the need to produce a test result in an acceptable period has to be taken into account. Briefly, two halves of a transmission synchromesh unit are repeatedly brought together under conditions of known force and speed differential until failure occurs. Failure may be defined in terms of synchromesh performance or overall wear.
  • the test rig used in the procedure was designed with consideration of work done by Socin and Walters, SAE Paper Number 680008 entitled “Manual Transmission Synchronizers”; Fano, CEC TLPG4 Chairman's Final Report, 1985, entitled “Synchromesh Test Method With Proposed Synchro Test Rig”; and Brugen, Thies and Naurian of Zahnradfabrik Friedrichshafen A.G. in a paper entitled “Einhne Des Schmierstoffes auf die Kunststoffmaschine Vonffygetrieben”.
  • the two synchromesh units are assembled in a gear box which forms the oil reservoir and facilitates splash lubrication of components. Drive may be transmitted along the main shaft or via the layshaft gears to give an increased ratio.
  • the input speed is kept constant by means of a DC drive control system and a large flywheel simulating vehicle inertia.
  • the output shaft accelerates and decelerates the small flywheel which simulates clutch inertia.
  • a pivot linkage connected to a pneumatic cylinder provides the actuating force which is measured by means of a load ring strain gauge.
  • a small heater is used to control oil temperature.
  • Torque transmitted through the output shaft can be measured to give an indication of the coefficient of friction between the synchronizing cones.
  • the synchromesh units used are standard commercially available steel units with a molybdenum-based plasma spray coating on the inner surface of the outer synchro-ring.
  • the syn-chromesh units are renewed before each test.
  • the coefficient of friction for satisfactory synchronizer performance in the test is at least 0.065.
  • Another performance criterion which may be used when performing the test for qualification purposes is excessive vibration of the gear box casing in the axial plane, a condition symptomatic of poor gear changes.
  • the control and monitoring of the rig is coordinated by a process controller.
  • a process controller During a test, which consists of 105 cycles, the number of poor changes is recorded. The test is terminated prematurely if this number becomes unacceptable.
  • Test components may be evaluated by inspecting the friction surface of the inner synchronizer cone using a Perthometer stylus device both before and after test. Polishing of the metal surface or the build up of a glaze of decomposed lubricant or additive yields an unacceptably smooth surface finish. This in turn causes low frictional values during the gear change and can lead to clash of the sleeve and gear clutch teeth. Wear measurements are also made on the test components.
  • reaction vessel To a reaction vessel are charged 38.0 parts of sulphurized isobutylene, 14.0 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl, 4.76 parts of dibutyl hydrogen phosphite, and 1.75 parts of 2-ethylhexyl acid phosphate. Throughout this addition, the components of the reaction vessel are agitated and maintained at 30°C for 10 minutes.
  • Primene® 81-R amine a tert-alkyl primary amine mixture in the C12-C14 range; Rohm & Haas
  • the mixture is stirred for 20 minutes without application of heat.
  • another 4.9 parts of this tertiary alkyl monoamine product is added and the contents of the reaction vessel are maintained at 50°C for 1 hour with continuous stirring.
  • 4.31 parts of oleic acid and 0.58 part of M530 defoamer an antifoam concentrate of Monsanto Company
  • reaction vessel To a reaction vessel are charged 38.3 parts of sulphurized isobutylene,14.3 parts of di-tert-nonyl polysulfide, 5.7 parts of dibutyl hydrogen phosphite, 0.1 part of tolyltriazole, and 2.9 parts of amyl acid phosphate. Throughout this addition, the components of the reaction vessel are agitated and maintained at 30°C for 10 minutes. To this mixture are added 3.7 parts of Primene 81-R amine, 3.7 parts of C16 and C18 primary amines, 1.0 part of octyl amine, and 3.2 parts of process oil, and the mixture is stirred for 20 minutes while maintaining the contents of the reaction vessel at 50°C for 1 hour with continuous stirring.
  • reaction vessel To a reaction vessel are charged 35.8 parts of sulphurized isobutylene, 3.6 parts of dibutyl hydrogen phosphite, 18.9 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl, and 1.7 parts of 2-ethylhexyl acid phosphate. Throughout this addition, the components of the reaction vessel are agitated and maintained at 30°C for 10 minutes.
  • reaction vessel To a reaction vessel are charged 35.1 parts of sulphurized isobutylene,3.8 parts of dibutyl hydrogen phosphite, 16.6 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl, and 1.0 part of 2-ethylhexyl acid phosphate. Throughout this addition, the components of the reaction vessel are agitated and maintained at 30°C for 10 minutes.
  • a gear lubricant is formulated using respective Examples A-D above as follows: Additive package 6.5% wt AMOCO 421 Magnesium Sulfonate 0.35% wt Diisodecyladipate 25% wt ETHYLFLO 174 PAO 58.15% wt ETHYLFLO 168 PAO 10.0% wt
  • a synthetic oil-based lubricating oil composition of this invention is formed by blending together the following components in the amounts specified: 6.5% of the additive package of Example A, B, C or D; 0.3% of HiTEC® 611 Calcium Sulfonate; 39.9% of ETHYLFLO 168 poly- ⁇ -olefin oligomer oil (an 8 cSt base oil) (ETHYLFLO is a trademark of Ethyl Corporation); 43.3% of a low chlorine version of ETHYLFLO 174 poly- ⁇ -olefin oligomer oil (a 40 cSt base oil); and 10.0% of KETJENLUBE synthetic oil (KETJENLUBE is a trademark of Akzo Chemicals).
  • a gear oil additive concentrate of this invention is formed by heating at 50°C for one hour a mixture of sulfurized isobutylene, trihydrocarbyl ester of dithiophosphoric acid, octyl amine, bis-2-ethylhexylphosphate, oleylamine, alkyl acid phosphite, a friction modifier and a succinimide type dispersant.
  • oleic acid, antifoam agent, and process oil are added to the hot mixture produced in the first stage.
  • the resultant concentrate is then allowed to cool to about 35°C, when metal deactivator and calcium sulfonate is added.
  • the resultant concentrate contains (apart from amine tied up with phosphorus acids) approximately 21 mole % of sulphur per mole of amino nitrogen and approximately 0.56 chemical equivalent of weak acid (oleic acid) per equivalent of amino nitrogen.
  • a gear oil is formed by blending this additive concentrate to a level of 6.5% w/w in an SAE 80W-90 synthetic fluid as in Example 10 above (equivalent to a concentration of 2.27 weight % of sulfurized isobutylene).
  • a mixture is formed from sulphurized isobutylene, oleylamine, octanoic acid, trihydrocarbyl dithiophosphate, a succinimide dispersant and a friction modifier in weight proportions of approximately 11.7:2.8:0.7:5.5:1:1 respectively.
  • This mixture is heated at 60°C for one hour.
  • octylamine, bis-2-ethylhexyl phosphate, an amine salt of a dihydrocarbyl thiophosphate and antifoam agent in weight proportions of approximately 0.2:0.4:3.3:0.2, respectively.
  • the resultant concentrate contains approximately 35% of the initial sulfurized isobutylene and approximately 18.3% of the mineral oil diluent.
  • the additive concentrate contains approximately 18 mole % of sulfur per mole of amino nitrogen and approximately 0.6 equivalent of weak acid per equivalent of amino nitrogen.
  • 3.25% of this additive package together with 0.3% of HiTEC® 611 calcium sulfonate is dissolved in a semi-synthetic fluid comprising 15% di(tridecyl)adipate, 25% ETHYLFLO 168 PAO, and 56.45% of mineral oil (Shell HVI 650b).
  • Example 12 for producing the additive concentrate is repeated with the following modifications: the bis-2- ethylhexyl phosphate, the octylamine and the antifoam agent are included in the first stage, the oleyl amine, the dispersant and the friction modifier are introduced into the second stage reaction mixture, and the second stage reaction mixture is held at 50°C for 30 minutes. 6.5% of this additive package together with 0.5% of Amoco 421 magnesium sulfonate is dissolved in a fluid comprising a mixture of ETHYLFLO 168 PAO and mineral oil (Shell HVI 650b) to give a gear lubricant of SAE 80W-90 viscosity grade.
  • a fluid comprising a mixture of ETHYLFLO 168 PAO and mineral oil (Shell HVI 650b) to give a gear lubricant of SAE 80W-90 viscosity grade.
  • Example 13 The procedure of Example 13 is repeated except that the first stage reaction mixture is heated to 50°C for 20 minutes and the second stage reaction mixture is held at 50°C for one hour. 6.5% of this additive package together with 0.25% of HiTEC®631 barium sulfonate is dissolved in a mixture of di(tridecyl)adipate (30%) and 63.25% mineral oil to give an SAE 80W-90 semi-synthetic gear lubricant.
  • Example 12 for producing the additive concentrate The procedure of Example 12 for producing the additive concentrate is repeated except that the octylamine is added in the first stage reaction, the octanoic acid is added in the second stage reaction mixture, the first stage reaction mixture is maintained at 50°C for one hour, and the amine salt of a dihydrocarbyl thiophosphate is added in a final stage along with the mineral oil and metal deactivator. 3.0% of HiTEC® 611 high base sulfonate is stirred into the additive package which is then used to formulate synthetic and semi-synthetic lubricants suitable for use in manual automotive transmissions where a synchronization system is utilized.
  • Example 12 for producing the additive concentrate is repeated with the following modifications: the octylamine and the trihydrocarbyl dithiophosphate are introduced into the first stage reaction mixture, and the octanoic acid is introduced into the second stage reaction mixture.
  • This additive package is dissolved at 5.0% together with 0.2% of Lubrizol 6477 high base sulfonate in a synthetic fluid comprising a mixture of 25% of a poly- ⁇ -olefin made from dodecene, 44.8% of a poly- ⁇ -olefin made from decene (ETHYLFLO 168 PAO) and 25% of di(tridecyl)adipate.
  • a lubricating fluid of SAE 90 grade viscosity characteristics is blended with a commercially available additive package (HiTEC® 2375 additive: Ethyl Petroleum Additives, Ltd.; Ethyl Petroleum Additives, Inc.; Ethyl S.A.; Ethyl Canada Limited) in quantities such that the oil contains sulfurized isobutylene (2.27% w/w) and an alkylamine/alkylphosphate/alkylphosphite/alkylthiophosphate mixture (0.56%w/w). The oil also contains octanoic acid in a proportion such that there are approximately 136 moles of sulfur per mole of said acid.
  • the sulfurized isobutylene itself is HiTEC® 309 additive.
  • the alkylamine is entirely neutralized by the phosphorus acids present. 3.75% of this additive package is used in combination with 0.2% HiTEC® 631 barium sulfonate to formulate a semi-synthetic lubricant comprising 15% di(isodecyl)adipate, 30% ETHYLFLO 168 PAO and 56.05% Shell mineral oil (HVI 650b).
  • Stage 1 To a reaction vessel are charged 43.4 parts of sulfurized isobutylene, 4.44 parts of dibutyl hydrogen phosphite, 4.99 parts of C12-C14 tertiary alkyl primary amine (Primene 81R; Rohm & Haas Chemical Company), 1.16 parts of 2-ethylhexyl acid phosphate, and 2.56 parts of process oil.
  • sulfurized isobutylene, phosphite and amines are added in the order named, the components of the reaction vessel are agitated.
  • An exothermic reaction occurs on bringing the sulfurized isobutylene, phosphite and amines into contact with each other, and the rate of addition is controlled so that the temperature does not exceed 60°C. Concurrently a slight negative pressure is maintained on the reaction vessel in order to remove any volatiles produced during the exothermic reaction. The temperature of the reaction vessel is maintained at 55-60°C for 60 minutes while continuing the agitation. The mixture is then cooled to 40°C.
  • Stage 2 In a separate reactor, 0.69 part of M-544 defoamant (Monsanto Chemical Company), 0.73 part of caprylic acid, 0.50 part of a mixture of C12 and C14 tert-alkyl primary monoamines (Primene 81R), and 2.87 parts of process oil are agitated together for 15 minutes.
  • the solution so formed is added to the Stage 1 product.
  • Concurrently, added is 19.63 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl. Agitation is continued for 15 minutes, and the temperature is kept at 30-40°C. The pH of the resultant solution is approximately 6.9.
  • Stage 3 To the agitated solution of Stage 2 are added 3.0 parts of 2-tert-dodecyldithio-1,3,4-thiadiazole and 16.03 parts of process oil. Agitation is continued for 15 minutes while keeping the temperature at 30-40°C.
  • the finished product is a bright clear amber liquid typically having a sulfur content of about 23.7% (wt) and a phosphorus content of about 2.35% (wt).
  • Stage 1 The procedure of Stage 1 of Example 18 is repeated using 34.97 parts of sulfurized isobutylene, 3.00 parts of dibutyl hydrogen phosphite, 5.60 parts of C16 ⁇ 18 alkyl monoamine, 0.01 part of n-octyl amine, 0.98 part of 2-ethylhexyl acid phosphate, and 2.65 parts of process oil.
  • Stage 2 The product of Stage 1 is cooled to 40°C with continued agitation. Added to this product after the temperature reaches 40°C, is 16.61 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl.
  • Stage 3 In a separate reactor, 0.58 part of M-544 defoamant (Monsanto Chemical Company), 0.62 part of caprylic acid, 0.62 part of a C36 dicarboxylic acid (formed by dimerization of oleic acid), and 2.65 parts of process oil are agitated together for 15 minutes. The resulting solution is added to the product from Stage 2. Agitation is continued for 15 minutes.
  • M-544 defoamant Monsanto Chemical Company
  • caprylic acid 0.62 part of a C36 dicarboxylic acid (formed by dimerization of oleic acid)
  • 2.65 parts of process oil are agitated together for 15 minutes.
  • the resulting solution is added to the product from Stage 2. Agitation is continued for 15 minutes.
  • Stage 4 To the agitated mixture of Stage 3 are added 2.6 parts of 2-tert-dodecyldithio-1,3,4-thiadiazole and 2.65 parts of process oil. After these two components are added, 0.75 parts of dibutyl hydrogen phosphite is added to the mixture. Agitation is continued for 15 minutes.
  • Stage 5 To the agitated mixture of Stage 4 are added 23.07 parts of a mixture composed of 55% (wt) of a boronated succinimide (HiTEC® 648 additive; Ethyl Petroleum Additives, Inc.; Ethyl Petroleum Additives, Ltd.; Ethyl S.A.; Ethyl Canada Ltd.) and 45% (wt) of process oil, and 2.65 parts of additional process oil. Agitation is continued for 15 minutes to ensure complete blending of the components. The finished product is pumped through a filter. The product is a bright clear amber liquid typically containing, on a weight basis, about 19.3% sulfur, about 2.0% phosphorus, about 0.62% nitrogen, and about 0.16% boron.
  • HiTEC® 648 additive Ethyl Petroleum Additives, Inc.
  • Ethyl Petroleum Additives, Ltd. Ethyl S.A.
  • Ethyl Canada Ltd. Ethyl Canada Ltd.
  • Agitation Agitation is continued for 15 minutes to
  • the synthetic fluid comprises 25% of a synthetic dibasic ester di(tridecyl)adipate and a 10 cSt (10 mm2.s ⁇ 1) poly- ⁇ -olefin, ETHYLFLO 170 PAO.
  • Stage 1 The procedure of Stage 1 of Example 18 is repeated using 31.26 parts of sulfurized isobutylene, 2.44 parts of dibutyl hydrogen phosphite, 3.18 parts of C16 ⁇ 18 alkyl monoamine, 0.63 part of n-octyl amine, 0.80 part of 2-ethylhexyl acid phosphate, and 5.19 parts of process oil.
  • the pH of the resulting mixture is approximately 7.0.
  • Stage 2 In a separate reactor, 0.47 part of M-544 defoamant (Monsanto Chemical Company), 0.51 part of caprylic acid, 0.51 part of C36 dicarboxylic acid (formed by dimerization of oleic acid), and 5.19 parts of process oil are agitated together for 15 minutes. The solution so formed is added to the Stage 1 product. Concurrently, added is 10.66 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl. Agitation is continued for 60 minutes, and the temperature is kept at 40°C.
  • M-544 defoamant Monsanto Chemical Company
  • caprylic acid 0.51 part of C36 dicarboxylic acid (formed by dimerization of oleic acid)
  • 5.19 parts of process oil are agitated together for 15
  • Stage 3 To the agitated solution of Stage 2 is added 2.14 parts of 2,5-dimethylthio-1,3,4-thiadiazole and 5.19 parts of process oil. Then 0.61 part of dibutyl hydrogen phosphite is added to the mixture. Agitation is continued for 15 minutes.
  • Stage 4 To the agitated solution from Stage 3 are added 10.32 parts of a mixture composed of 55% (wt) of a boronated succinimide (HiTEC® 648 additive; Ethyl Petroleum Additives, Inc.; Ethyl Petroleum Additives, Ltd.; Ethyl S.A.; Ethyl Canada Ltd.) and 45.% (wt) of process oil, 6.24 parts of alkenylsuccinimide (formed from ammonia and alkenyl succinic anhydride produced from a mixture of olefins made by isomerizing a 1-olefin mixture containing 49% C20, 42% C22, and 8% C24 1-olefins, and 14.66 parts of additional process oil.
  • a boronated succinimide HiTEC® 648 additive; Ethyl Petroleum Additives, Inc.; Ethyl Petroleum Additives, Ltd.; Ethyl S.A.; Ethyl Canada Ltd.
  • the finished product is pumped through a filter.
  • the product is a bright clear amber liquid typically containing, on a weight basis, about 17.5% sulfur, and about 1.6% phosphorus.
  • This product is dissolved in a fluid comprising 0.5% calcium sulfonate (HiTEC® 611 additive), 27% Lubrizol 3174 shear stable viscosity index improver, 40% of a synthetic ester di(isodecyl)adipate and 32.5% of ETHYLFLO 168 PAO.
  • An additive concentrate is prepared as follows:
  • a tertiary alkyl primary amine (PRIMENE 81R) is added and allowed to react. After approximately 30 minutes a polyisobutylene substituted succinimide dispersant at 2.42 parts by weight and a further 4.9 parts of PRIMENE 81R is added and the resultant mixture stirred at about 55°C for one hour.
  • Example E Into the additive concentrate prepared as in Example E above are blended 1.0 part of sodium alkyl benzene sulfonate, 2.0 parts of HiTEC® 611 calcium sulfonate and 12.0 parts of mineral oil.
  • a chemical composition is prepared as follows:
  • composition formed as described in Example F above is mixed 50:50 by weight with calcium sulfonate (HiTEC 611 additive and used in formulating transmission oils as described in Example 27 below.
  • Example 26 Composition of Example 26 0.2 1.0 0.3 0.2 0.9 1.0 Composition of Example F 3.75 7.5 -- -- -- -- -- Anglamol 99 (Low Chlorine) -- -- -- 3.9 -- -- -- -- Anglamol 9000 -- -- -- -- -- 7.0 -- Mobilab G521T -- -- -- -- -- -- 5.0 Diisodecyladipate 10.0 20.0 20.0 20.0 25.0 20.0 ETHYLFLO 168 PAO -- 11.5 -- 10.0 17.1 -- ETHYLFLO 170 PAO 80.0 -- 70.0 -- -- 74.0 ETHYLFLO 174 PAO 6.05 -- 5.8 -- -- -- Mineral oil (Shell HV1650b) -- 60 -- 64.8 50 --
  • a semi-synthetic gear fluid of this invention is formed from Anglamol 99 gear additive package at 3.9% and barium sulfonate (HiTEC 631 additive) at 0.2% in a mixture of 10% diisodecyl adipate, 25% hydrotreated mineral oil (Shell XHVI 5.2) and 60.9% mineral oil (Shell HVI 650b).
  • Blended together are Anglamol 6004A gear additive package at 6.5%, HiTEC 614® calcium sulfonate at 0.5%, diisodecyladipate at 10%, ETHYLFLO 174 PAO at 6.0% and ETHYLFLO 170 PAO at 77% to give an SAE 80W fluid of this invention.
  • a semi-synthetic gear lubricant of the invention is formed when 8.0% of Anglamol 6043U gear additive is blended with 0.2% HiTEC 631 barium sulfonate, 35% of di(tridecyl) adipate and 56.8% of mineral oil (Shell HVI 650b).
  • Blended together are 6.5% of a low chlorine version of Anglamol 99 gear additive, 0.5% HiTEC 631 barium sulfonate, 1.5% HiTEC 623 pour point depressant, 65% mineral oil (Shell HVI 650b) and 26.5% of ETHYLFLO 168 PAO to give a semisynthetic gear lubricant of the invention.
  • a semi-synthetic gear lubricant of the invention is formed when 8.0% of Anglamol 6043U gear additive is blended with 0.1% potassium alkylbenzene sulfonate, 0.1% HiTEC 611 calcium sulfonate, 35% di(tridecyl)adipate and 56.8% of mineral oil.
  • Blended together are 6.5% of a low chlorine version of Anglamol 99 gear additive, 0.2% sodium alkylbenzene sulfonate, 0.2% Amoco 421 magnesium sulfonate, 0.2% HiTEC 614 calcium sulfonate, 1.5% HiTEC 623 pour point depressant, 65% mineral oil (Shell HVI 650b) and 26.5% of diisodecyladipate to give a lubricant of the invention suitable for use in manual transmissions and final drives of certain motor vehicles.
  • the above Shell HVI 115 mineral oil was a solvent neutral oil having a kinematic viscosity of 9 mm2.s ⁇ 1 (cSt) at 100°C containing 1.0 HiTEC® 623 pour point depressant.
  • the first seven tests in Table I i.e., Run Nos. 1-7) used SAE 80W viscosity grade formulations. Run Nos. 1-7 are comparative tests as none of these formulations contained a sulfonate additive. However, Run No. 8 used a formulation containing 0.5 wt% of HiTEC® 611 additive, an overbased calcium alkylbenzene sulfonate having a nominal TBN of 300 available commercially from Ethyl Petroleum Additives, Inc.
  • the HiTEC 611 additive contains approximately 44% diluent oil.
  • the formulation of Run No. 8 is an SAE 90 grade formulation useful as a total driveline fluid suitable for use in final drives such as hypoid differentials, as well as gear boxes. TABLE I Run No. % HiTEC 380 % PAO (I) % ESTER % MIN.
  • OIL %PAO (II) ZF RESULTS 1 3.2 -- -- 96.8 -- PASS 2 3.2 96.8 -- -- -- FAIL 3 3.2 86.8 10 -- -- FAIL 4 6.5 86.8 10 -- -- FAIL 5 3.2 71.8 25 -- -- FAIL 6 3.2 71.8 25 -- -- FAIL 7 3.2 36.8 -- 60 -- FAIL 8 6.5 32.2 10 -- 50.8 PASS
  • Run No. 8 shows that inclusion in the synthetic oil based fluid of a small amount of a metal sulfonate pursuant to this invention improved the frictional properties of the blend to such an extent that it passed the test.
  • Table II summarizes the results of additional ZF.Synchronizer tests which demonstrate the practice and advantages of this invention.
  • Run Nos. 11-14 represent the practice of this invention as these gear oils contained, respectively, 2.0, 1.0, 0.2 and 0.1% of a metal sulfonate (HiTEC® 611 additive).
  • the gear oil contained, for comparative purposes, 1.0% of an alkenyl succinimide friction modifier of the type described in EP 20,037.
  • the oil of Run No. 16 contained 3.5% of a polyisobutenyl succinimide ashless dispersant (HiTEC® 646 additive; Ethyl Petroleum Additives, Inc.; Ethyl Petroleum Additives, Ltd. and their affiliated companies). The foregoing percentages are on an "as received basis" and thus include solvent oils.
  • oil-soluble is used in the sense that the component in question has sufficient solubility in the selected base oil in order to dissolve therein at ordinary temperatures to a concentration at least equivalent to the minimum concentration specified herein for use of such component.
  • solubility of such component in the selected base oil will be in excess of such minimum concentration, although there is no requirement that the component be soluble in the base oil in all proportions.
  • certain useful additives do not completely dissolve in base oils but rather are used in the form of stable suspensions or dispersions. Additives of this type can be employed in the compositions of this invention, provided they do not significantly interfere with the performance or usefulness of the composition in which they are employed.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Lubricants (AREA)

Abstract

Gear oils and gear oil additive packages that exhibit improved frictional properties for use in transmissions equipped with synchronizers are described. The lubricant compositions have a kinematic viscosity at 100°C in the range of 4 to 32 mm².s⁻¹ (cSt), and comprise a) a base oil having at least 25%, preferably at least 50%, more preferably least 75%, and most preferably 100% by weight of (i) hydrogenated poly-alpha-olefin oligomer oil or (ii) synthetic ester oil, or (iii) a combination of (i) and (ii); b) an amount of a gear oil additive package such that the gear oil lubricant satisfies or exceeds the specifications for API-GL4 service; and c) an amount in the range of 0.01 to 2 wt % based on the total weight of the lubricant of at least one alkali or alkaline earth metal salt of an oil-soluble sulfonic acid, the amount of said metal salt used being sufficient to improve the friction properties of the lubricant for use in manual transmissions, particularly those of the synchronizer type; said lubricant containing at most 100 ppm of metal as one or more additive components other than said metal salt, and having on a weight basis a boron content, if any, of not more than 1,000 ppm.

Description

  • This invention relates to improving the frictional characteristics of gear oils in which the base oil is, or contains a significant quantity of, a synthetic oil such as a polyalpha-olefin oil (PAO) or a synthetic ester oil.
  • Modern commercial large vehicles equipped with manual transmissions of the synchronizer type are typically operated with conventional mineral oil-based transmission lubricants. Such lubricants contain additives for wear protection, corrosion protection, and other beneficial property improvements. The level and type of additive used depends on the performance requirements of the oil, including low temperature properties, or wear protection. Performance designations which are used include API-GL4 and API-GL5. More recently PG1, PG2 and API-GL7 are being defined. Additionally a degree of demulsification may be preferred. API-GL4 and lower performance specifications may be met using conventional crankcase mineral oil lubricants containing conventional levels of zinc dialkydithiophosphates, sulfonates, or ashless dispersants. Mineral oil lubricants to meet all the above levels are based on P/S essentially ashless formulations, although up to at least API-GL5 has been met by P/S formulations containing significant levels of alkali metal borates and metal sulfonates (e.g., OLOA 9750 additive). As those skilled in the art are aware, "P/S" refers to gear oil additive packages in which a phosphorus and sulfur-containing antiwear and/or extreme pressure additive system is employed.
  • However, at the more extreme temperatures and other extreme conditions which many modern vehicles meet, great advantage may be obtained by utilizing fluids other than the more traditional mineral oils to formulate the transmission fluids. These synthetic fluids, as they are often termed, may be used with mineral oil or on their own. The synthetic oils/fluids of principal interest in this context comprise poly-α-olefin oils (PAO) and synthetic ester oils because of their thermal stability and desirable viscometric properties.
  • Unfortunately, unlike the traditional mineral oil-based transmission fluids, many of the synthetic fluids, which are based on the P/S essentially ashless additive systems, afford unsuitably low frictional properties in the synchronizer-based transmissions and thus cause poor synchronization of the gear changes. This negative aspect of such synthetic based gear oils may be conveniently observed as low friction and noisy gear change in the Zahnradfabrik Friedrichshafen A.G. synchronizer test (described and referred to hereinafter as the "ZF.Synchronizer test"). To rectify this problem it is usually necessary to cause an appropriate increase in the frictional properties of the finished synthetic oil-based lubricant. But in doing so, it is important not to materially interfere with the other performance qualities of the finished gear oil.
  • It has now been found possible to beneficially increase the friction exhibited by finished gear lubricants based on synthetic oils such as PAO and synthetic ester oil and blends thereof by means of small amounts of an additive which will not materially affect the other performance capabilities of the finished lubricant. For example, as little as 0.1 wt % of a preferred additive in the oil, has enabled the finished lubricant to pass the ZF.Synchronizer test conducted in the manner described hereinafter.
  • The additives used pursuant to this invention are alkali or alkaline earth metal salts of oil-soluble sulfonic acids, such as petroleum sulfonic acids, preferably alkylaryl sulfonic acids and, more preferably, alkylbenzene sulfonic acids. The metals of such salts preferably are those which have low toxicity and which present little or no concern from the environmental standpoint, namely, lithium, sodium, potassium, magnesium, and calcium. However, barium and strontium sulfonates can be used, if desired.
  • So far as is known, there have been only two types of API-GL5 gear oil compositions used in actual practice that apparently contain a metal sulfonate component. One is SPIRAX MB 90 (trademark of the Shell Oil Companies), a conventional mineral oil-based gear oil, which in Germany contained small amounts of barium, believed to be in the form of a barium sulfonate corrosion inhibitor.
  • The other type is based on use of gear oil additive packages containing high levels of potassium borate dispersion serving as an antiwear/extreme pressure agent. These packages are believed to contain low levels of calcium, presumably in the form of a sulfonate. These packages are apparently used primarily (if not exclusively) in conventional mineral oil stocks in forming finished gear oils. And in any event, the levels of the potassium borate used in the finished oils (e.g., 1-2 wt%) are sufficiently high as to seriously impair the results obtainable by the practice of this invention and thus are outside of the permissible concentrations of this invention.
  • Further information concerning such dispersed potassium borate additive systems may be found in C.G. Salentine, SAE Technical Paper 880609 (1988) entitled "New Gear Lubricant Technology Using a Solid Lubricant Dispersion", and G.E. Callis and G.Y. Suh, SAE Technical Paper 831731 (1983) entitled "Durability Testing of Low Viscosity Borate Gear Lubricants". See also U.S. Pat. Nos. 3,313,727; 3,565,802; 3,819,521; 3,846,313; 3,853,772; 3,912,639; 3,912,644; 3,929,650; 3,997,454; 4,089,790; and 4,163,729.
  • Thus in accordance with one embodiment of this invention, there is provided a gear oil lubricant having a kinematic viscosity at 100° C in the range of 4 to 32 mm².s⁻¹ (cSt), and preferably in the range of 8 to 20 mm².s⁻¹ (cSt), and comprising:
    • a) a base oil having at least 25%, preferably at least 50%, more preferably least 75%, and most preferably 100% by weight of (i) hydrogenated poly-alpha-olefin oligomer oil or (ii) synthetic ester oil, or (iii) a combination of (i) and (ii);
    • b) an amount of a gear oil additive package such that the gear oil lubricant satisfies or exceeds the specifications for GL4 service; and
    • c) an amount in the range of 0.01 to 2 wt % based on the total weight of the lubricant of at least one alkali or alkaline earth metal salt of an oil-soluble sulfonic acid, the amount of said metal salt used being sufficient to improve the friction properties of the lubricant for use in manual transmissions, particularly those of the synchronizer type; said lubricant being essentially free of any metal additive component (i.e., the lubricant contains at most 100 ppm and preferably no more than 50 ppm of metal as one or more additive components other than said metal salt), and having on a weight basis a boron content, if any, of not more than 1,000 ppm, preferably not more than 300 ppm, and most preferably not more than 25 ppm.
  • It is to be noted that in the ZF.Synchronizer test the beneficial increase in friction exhibited by finished gear lubricants of this invention manifests itself in a substantial increase in the number of cycles during which the test can be performed without poor synchronization of the gear changes. For example, a finished synthetic oil-based gear oil devoid of a metal sulfonate additive may encounter substantial failure within 10,000 or 15,000 cycles. On the other hand, finished synthetic oil-based lubricants of this invention which contain a metal sulfonate component can achieve at least 50,000 and usually at least 100,000 cycles of trouble free operation in this test procedure.
  • It will be appreciated that in satisfying or exceeding the specifications for API-GL4 service, the gear oil additive package used as component b) may in fact satisfy the requirements for other performance specifications such as API-GL5, and including specifications not yet in being (or even envisioned) such as PG1, PG2 and API-GL7 or specifications of other countries such as comparable JIS gear oil standards, or the like. In short, the specifications of API-GL4 are to be considered minimum performance levels for the package. For example, if the requirements of the API-GL7 specification are more stringent for the most part than, say, API-GL4, the fact that an additive package satisfies the API-GL7 requirements inherently satisfies the minimum performance requirements for use in the practice of this invention, whether or not the package has actually been subjected to the API-GL4 performance tests.
  • Pursuant to another embodiment of this invention, there is provided a gear oil additive package which comprises (1) an oil-soluble phosphorus and sulfur-containing antiwear and/or extreme pressure additive complement and (2) at least one alkali or alkaline earth metal salt of an oil-soluble sulfonic acid; said gear oil additive package being further characterized in that when blended with a base oil having a kinematic viscosity in the range of 4 to 32 cSt at 100°C and composed of at least 25% by volume of (i) hydrogenated poly-alpha-olefin oligomer oil or (ii) synthetic ester oil, or (iii) a combination of (i) and (ii) to form a lubricant containing from 0.01 to 2 wt % of said metal salt, said gear oil additive package provides a lubricant composition that:
    • A) satisfies or exceeds the specifications for API-GL4 service;
    • B) contains, if any, at most 100 ppm and preferably no more than 50 ppm of metal apart from the metal of said metal salt; and
    • C) has a boron content, if any, of not more than 1,000 ppm, preferably not more than 300 ppm, and most preferably not more than 25 ppm.
  • Still another aspect of this invention is the method of beneficially modifying the frictional characteristics of a low-friction synthetic lubricant composition containing a gear oil additive package such that the lubricant composition satisfies or exceeds the specifications for API-GL4 service, but does not exhibit satisfactory friction properties for use in manual transmissions, particularly those of the synchronizer type. The method comprises including in such lubricant composition an amount in the range of 0.01 to 2 wt % based on the total weight of the lubricant of at least one metal salt of an oil-soluble sulfonic acid such that the friction properties of said lubricant are improved for use in manual transmissions, particularly those of the syn-chronizer type.
  • In each of the above embodiments the metal of the sulfonate salt preferably is lithium, sodium, potassium, magnesium, or calcium, or a combination of two or more such metals. However, barium and/or strontium sulfonates can be used if desired.
  • In each of the embodiments of this invention, the metal sulfonate can be employed as a separate component (e.g., as a "top-treat" to the base oil with which the additive package has been or will be blended) or as a component of the additive package itself. Similarly, while use of additive packages is preferred, it is possible to blend the metal sulfonate and the respective components of the additive package into the base oil individually or in various compatible sub-combinations.
  • As noted above, the base oils are composed partially or entirely of a low-friction fluid such as PAO base oil and/or a synthetic ester lubricating oil. The PAO fluids are usually formed by oligomerization or co-oligomerization of 1-alkene hydrocarbon having 6 to 20 and preferably 8 to 16 carbon atoms in the molecule and hydrogenation of the resultant oligomer. Hydrogenated oligomers formed from 1-decene are particularly preferred. Methods for the production of such liquid oligomeric 1-alkene hydrocarbons are known and reported in the literature. See for example U. S. Pat. Nos. 3,763,244; 3,780,128; 4,172,855; 4,218,330; and 4,950,822. Additionally, suitable hydrogenated 1-alkene oligomers of this type are available as articles of commerce, for example, from Ethyl Corporation and its affiliates under the trade mark ETHYLFLO.
  • Synthetic ester oils are also well known and widely available in the marketplace. Typical synthetic ester oils include such materials as the esters of dicarboxylic acids (e.g., phthalic acid, succinic acid, maleic acid, azelaic acid, suberic acid, sebacic acid, fumaric acid, adipic acid, linoleic acid dimer) with a variety of alcohols (e.g., butyl alcohol, hexyl alcohol, dodecyl alcohol, 2-ethylhexyl alcohol, ethylene glycol). Specific examples of these esters include dibutyl adipate, di(1-ethylpropyl) adipate, di(1,3-dimethylbutyl) adipate, di(2-ethylhexyl) adipate, didodecyl adipate, di(tridecyl) adipate, di(2-ethylhexyl) sebacate, dilauryl sebacate, di-n-hexylfumarate, dioctyl sebacate, di(1-methylpropyl) azelate, diisooctyl azelate, diisodecyl azelate, dioctyl phthalate, didecyl phthalate, mixed C₉ and C₁₁ dialkyl phthalate, dibutyl sebacate, di(1-ethylpropyl) sebacate, di(eicosyl) sebacate, the 2-ethylhexyl diester of linoleic acid dimer, and the complex ester formed by reacting one mole of sebacic acid with two moles of tetraethylene glycol and two moles of 2-ethylhexanoic acid. Other synthetic esters which may be used as synthetic oils include those made from C₃-C₁₂ monocarboxylic acids and polyols and polyol ethers such as neopentyl glycol, trimethylolpropane, pentaerythritol and dipentaerythritol. Trimethylol propane tripelargonate and pentaerythritol tetracaproate serve as examples.
  • Suitable commercially available products include Emkarate 911P (ICI, plc.), and KETJENLUBE synthetic oil (Akzo Chemicals).
  • The base oils may contain up to 75%, preferably no more than 50%, and more preferably no more than 25% by weight of a mineral oil or other suitable oleaginous liquid of lubricating viscosity, provided the overall base lubricant is suitable for use in forming a finished gear lubricant that satisfies or exceeds the specifications for API-GL4 service, and provided further that the resultant finished oil remains amenable to friction improvement pursuant to this invention. It will be understood that most gear oil packages contain diluent oils or solvents for certain active ingredients or components. However, since such diluent oils or solvents are added to the base oil along with the additive package or with one or more additive components blended separately or individually into the base oil, such diluent oils or solvents are to be omitted from consideration when assessing the makeup of the base oil of the compositions of this invention. Thus the finished gear oil lubricant may contain up to 75% by weight of a mineral oil or the like, plus an additional amount of diluent oil or solvent emanating from the additives or additive package used in formulating the finished lubricant.
  • The metal sulfonates used in the invention are preferably overbased metal sulfonates, but the so-called neutral metal sulfonates can be used, if desired. The use of calcium salts of oil-soluble alkylbenzene sulfonates, especially overbased calcium alkylbenzene sulfonates, is particularly preferred. Methods for forming metal sulfonates are described for example in U.S. Pat. Nos. 2,865,956; 2,956,018; 2,671,430; 3,779,920; 3,907,691; 4,137,184; 4,261,840; 4,326,972; 4,328,111; 5,089,155; and 5,112,506. Petroleum sulfonates are usually prepared by the sulfonation of suitable petroleum fractions with subsequent removal of acid sludge and purification followed by neutralization with the appropriate basic metal compound (e.g., oxide or hydroxide). Petroleum oxidates such as described in EP Pub. No. 275,395 (published July 27, 1988) can be used in forming overbased sulfonates. Alkylaryl sulfonates are usually prepared by sulfonation of alkylated benzene or benzene analogs (toluene, naphthalene, phenothiazine, diphenyl oxide, or diphenyl sulfide), followed by workup and neutralization. For example alkylbenzenes suitable for producing the sulfonates can be formed by alkylating benzene with an oligomer or polymer such as tetrapropylene in the presence of an Friedel-Crafts catalyst. A number of highly suitable metal sulfonates are available as articles of commerce.
  • Quantities ranging from as little as 0.01 % wt % up to as much as 2 % by wt % or more of the metal sulfonate based on the total weight of the finished lubricant can be employed. Ordinarily the amount used will not be greatly in excess of that amount needed to yield the friction performance desired in the particular finished gear oil lubricant in question. Thus often the amount will not be above 1 wt %, and in some cases will not exceed 0.5 wt %. In the case of the friction-improved additive packages of this invention, the amount will be proportioned such that when the package is blended into the base oil at the recommended or desired concentration, the resultant finished oil will contain from 0.01 wt % up to 2 wt % or more, preferably up to about 1 wt %, and in some cases up to about 0.5 wt % of the metal sulfonate. It is to be noted that these proportions of the metal sulfonate are based on the active ingredient, and thus the weight of any solvent or diluent associated with the metal sulfonate as used should be subtracted from the additive weight when calculating the concentration of metal sulfonate in the finished oil or in the friction-improved additive package. However the total weight of the finished oil or of the completed additive package will include the weight of such solvent or diluent.
  • The specifications for API-GL4 and API-GL5 service are published in ASTM Publication STP-512A entitled "Laboratory Performance Tests for Automotive Gear Lubricants" (March 1987).
  • A number of gear oil additive packages (concentrates) that provide API-GL4 or API-GL5 performance are available in the marketplace. They generally contain at least a sulfur-phosphorus antiwear or extreme pressure additive system, one or more antioxidants, one or more corrosion inhibitors, and an antifoam additive, and may, and preferably do, contain a dispersant additive.
  • Pursuant to another embodiment of this invention, there is provided a gear oil additive package (concentrate) which comprises:
    • a) at least one oil-soluble ashless dispersant, preferably a succinimide ashless dispersant and/or a succinic ester-amide ashless dispersant, and more preferably a Mannich base ashless dispersant;
    • b) at least one oil-soluble metal-free sulphur-containing antiwear and/or extreme pressure agent;
    • c) at least one oil-soluble metal-free phosphorus-containing antiwear and/or extreme pressure agent; and
    • d) at least one alkali or alkaline metal salt of an oil-soluble sulfonic acid in an amount such that a lubricant composition formed by blending the additive package in a base oil having a kinematic viscosity in the range of 4 to 32 cSt at 100°C and composed of at least 25% by weight, preferably at least 50% by weight, and most preferably at least 75% by weight of (i) hydrogenated polyalpha-olefin oligomer oil or (ii) synthetic ester oil, or (iii) a combination of (i) and (ii) to form a lubricant containing from 0.01 to 2 wt % of said metal salt:
    • A) satisfies or exceeds the specifications for API-GL4 service;
    • B) contains, if any, no more than at most 100 ppm and preferably no more than 50 ppm of metal apart from the metal of said metal salt; and
    • C) has a boron content, if any, of not more than 1,000 ppm, preferably not more than 300 ppm, and most preferably not more than 25 ppm.

    Preferably, the metal of such salt is lithium, sodium, potassium, magnesium, or calcium, or a combination of two or more such metals.
  • A finished lubricant composition containing at least the foregoing components a), b), c) and d) constitutes still another embodiment of this invention. Such finished lubricant satisfies or exceeds the specifications for API-GL4 service, and preferably satisfies or exceeds the specifications for API-GL5 service. Component a) of the foregoing additive package and finished lubricant composition most preferably is a Mannich base which includes or, alternatively, consists of boronated Mannich base ashless dispersant.
  • Yet another embodiment of this invention involves using as component a) a Mannich base dispersant and proportioning components a) and b) above in the additive package or in the finished lubricant composition such that the mass ratio (wt/wt) of nitrogen in the Mannich base dispersant to sulphur in the sulphur-containing antiwear and/or extreme pressure agent is in the range of 0.0005:1 to 0.5:1, and preferably in the range of 0.003:1 to 0.2:1.
  • In still further embodiments a Mannich base dispersant is employed as component a) and components a) and c) above are proportioned in the additive package or in the finished lubricant such that the mass ratio (wt/wt) of nitrogen in the Mannich base dispersant to phosphorus in the metal-free phosphorus-containing antiwear and/or extreme pressure agent is in the range of 0.005:1 to 5:1, and preferably in the range of 0.01:1 to 2:1.
  • In additional embodiments, any of the above additive concentrates and finished lubricant compositions further comprise at least one oil-soluble demulsifying agent.
  • In still other embodiments, any of the above additive concentrates and finished lubricant compositions further comprise at least one oil-soluble amine salt of a sulphur-free hydrocarbyl phosphoric acid.
  • Preferably the lubricant compositions of this invention have a halogen content, if any, of no more than 100 ppm, and more preferably no more than 30 ppm on a weight basis.
  • Other embodiments of this invention will appear hereinafter.
  • As is well known in the art, the ZF.Synchronizer test has been designed for the evaluation of oil performance in commercially available synchromesh units under endurance conditions with the bulk lubricant temperature controlled at a relatively high level. While it is important to simulate fairly closely the actual conditions met in service, the need to produce a test result in an acceptable period has to be taken into account. Briefly, two halves of a transmission synchromesh unit are repeatedly brought together under conditions of known force and speed differential until failure occurs. Failure may be defined in terms of synchromesh performance or overall wear. The test rig used in the procedure was designed with consideration of work done by Socin and Walters, SAE Paper Number 680008 entitled "Manual Transmission Synchronizers"; Fano, CEC TLPG4 Chairman's Final Report, 1985, entitled "Synchromesh Test Method With Proposed Synchro Test Rig"; and Brugen, Thies and Naurian of Zahnradfabrik Friedrichshafen A.G. in a paper entitled "Einfluss Des Schmierstoffes auf die Schaltelemente Von Fahrzeuggetrieben". The two synchromesh units are assembled in a gear box which forms the oil reservoir and facilitates splash lubrication of components. Drive may be transmitted along the main shaft or via the layshaft gears to give an increased ratio. The input speed is kept constant by means of a DC drive control system and a large flywheel simulating vehicle inertia. On changing gear, the output shaft accelerates and decelerates the small flywheel which simulates clutch inertia. A pivot linkage connected to a pneumatic cylinder provides the actuating force which is measured by means of a load ring strain gauge. A small heater is used to control oil temperature.
  • Torque transmitted through the output shaft can be measured to give an indication of the coefficient of friction between the synchronizing cones. The synchromesh units used are standard commercially available steel units with a molybdenum-based plasma spray coating on the inner surface of the outer synchro-ring. The syn-chromesh units are renewed before each test. Typically, when measured at a point of relatively high torque during a gear change, the coefficient of friction for satisfactory synchronizer performance in the test is at least 0.065.
  • Another performance criterion which may be used when performing the test for qualification purposes is excessive vibration of the gear box casing in the axial plane, a condition symptomatic of poor gear changes. For this purpose the control and monitoring of the rig is coordinated by a process controller. During a test, which consists of 10⁵ cycles, the number of poor changes is recorded. The test is terminated prematurely if this number becomes unacceptable.
  • Test components may be evaluated by inspecting the friction surface of the inner synchronizer cone using a Perthometer stylus device both before and after test. Polishing of the metal surface or the build up of a glaze of decomposed lubricant or additive yields an unacceptably smooth surface finish. This in turn causes low frictional values during the gear change and can lead to clash of the sleeve and gear clutch teeth. Wear measurements are also made on the test components.
  • As those skilled in the art already know, arrangements can be made with Zahnradfabrik Friedrichshafen A.G. whereby that company will perform the ZF.Synchronizer test on formulations submitted by a party for test. It is understood that a summary report of the results of the test is provided to the submitter of the test formulation.
  • The following examples numbered 1 through 35 illustrate, inter alia, preferred additive concentrates and oleaginous compositions of this invention. These examples are not intended to limit, and should not be construed as limiting, this invention. In all of the examples, all percentages are by weight.
  • EXAMPLE A
  • To a reaction vessel are charged 38.0 parts of sulphurized isobutylene, 14.0 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl, 4.76 parts of dibutyl hydrogen phosphite, and 1.75 parts of 2-ethylhexyl acid phosphate. Throughout this addition, the components of the reaction vessel are agitated and maintained at 30°C for 10 minutes. To this mixture is added 6.0 parts of Primene® 81-R amine (a tert-alkyl primary amine mixture in the C₁₂-C₁₄ range; Rohm & Haas), and the mixture is stirred for 20 minutes without application of heat. Then another 4.9 parts of this tertiary alkyl monoamine product is added and the contents of the reaction vessel are maintained at 50°C for 1 hour with continuous stirring. While cooling the vessel contents to 40°C, 4.31 parts of oleic acid and 0.58 part of M530 defoamer (an antifoam concentrate of Monsanto Company) are added. Then, in a final stage and without application of heat, 1.8 parts of 2-tert-dodecyldithio-5-mercapto-1,3,4-thiadiazole, 12.3 parts of Amoco 9250 additive (a proprietary product of Amoco Corporation, which is believed to be a 48% oil concentrate of boronated Mannich base ashless dispersant and which contains about 1.1% nitrogen and about 0.2% boron), 0.77 parts of Pluronic L-121 demulsifier (an ethylene oxide-propylene oxide block copolymer of BASF Corporation) and 10.83 parts of process oil are added to the contents of the reaction vessel. The resulting additive concentrate is stirred for 60 minutes.
  • EXAMPLE B
  • To a reaction vessel are charged 38.3 parts of sulphurized isobutylene,14.3 parts of di-tert-nonyl polysulfide, 5.7 parts of dibutyl hydrogen phosphite, 0.1 part of tolyltriazole, and 2.9 parts of amyl acid phosphate. Throughout this addition, the components of the reaction vessel are agitated and maintained at 30°C for 10 minutes. To this mixture are added 3.7 parts of Primene 81-R amine, 3.7 parts of C₁₆ and C₁₈ primary amines, 1.0 part of octyl amine, and 3.2 parts of process oil, and the mixture is stirred for 20 minutes while maintaining the contents of the reaction vessel at 50°C for 1 hour with continuous stirring. Then, while cooling the contents to 40°C, 0.6 part of C₃₆ dimer acid, 0.6 part of caprylic acid, 1.0 part of M530 defoamer, and 3.2 parts of process oil are added. Thereafter, without application of heat, 2.7 parts of 2-tert-dodecyldithio-5-mercapto-1,3,4-thiadiazole, 12.2 parts of Amoco 9250 additive, 0.5 part of Pluronic L-101 demulsifier (an ethylene oxide-propylene oxide block copolymer concentrate of BASF Corporation), 2.9 parts of phenolic antioxidant (ETHYL® antioxidant 733) and 3.4 parts of process oil are added to the contents of the reaction vessel. The resulting additive concentrate is stirred for 60 minutes.
  • EXAMPLE C
  • To a reaction vessel are charged 35.8 parts of sulphurized isobutylene, 3.6 parts of dibutyl hydrogen phosphite, 18.9 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl, and 1.7 parts of 2-ethylhexyl acid phosphate. Throughout this addition, the components of the reaction vessel are agitated and maintained at 30°C for 10 minutes. To this mixture are added 3.9 parts of C₁₆ and C₁₈ primary amines, 0.7 part of octyl amine, and 9.1 parts of process oil, and the mixture is stirred for 20 minutes while maintaining the contents of the reaction vessel at 50°C for 1 hour with continuous stirring. Then, while cooling the contents to 40°C, 0.7 part of caprylic acid, 0.7 part of M544 defoamer (an acrylate copolymer concentrate of Monsanto Company), and 5.8 parts of process oil are added. Thereafter, without application of heat, 12.0 parts of Amoco 9250 additive,1.5 parts of 2-tert-dodecyldithio-5-mercapto-1,3,4-thiadiazole, 0.8 part of Chemax HCO-5 (a hydrogenated castor oil ethoxylate concentrate of Chemax, Inc.), and 4.8 parts of process oil are added to the contents of the reaction vessel. The resulting additive concentrate is stirred for 60 minutes.
  • EXAMPLE D
  • To a reaction vessel are charged 35.1 parts of sulphurized isobutylene,3.8 parts of dibutyl hydrogen phosphite, 16.6 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl, and 1.0 part of 2-ethylhexyl acid phosphate. Throughout this addition, the components of the reaction vessel are agitated and maintained at 30°C for 10 minutes. To this mixture are added 3.3 parts of C₁₆ and C₁₈ primary amines, and 8.3 parts of process oil, and the mixture is stirred for 20 minutes while maintaining the contents of the reaction vessel at 50°C for 1 hour with continuous stirring. Then, while cooling the contents to 40°C, 0.6 part of caprylic acid, 0.6 part of M544 defoamer, and 8.3 parts of process oil are added. Thereafter, without application of heat, 12.8 parts of Amoco 9250 additive, 1.3 parts of 2-tert-dodecyldithio-5-mercapto-1,3,4-thiadiazole, and 8.3 parts of process oil are added to the contents of the reaction vessel. The resulting additive concentrate is stirred for 60 minutes.
  • EXAMPLES 1-4
  • A gear lubricant is formulated using respective Examples A-D above as follows:
    Additive package 6.5% wt
    AMOCO 421 Magnesium Sulfonate 0.35% wt
    Diisodecyladipate 25% wt
    ETHYLFLO 174 PAO 58.15% wt
    ETHYLFLO 168 PAO 10.0% wt
  • EXAMPLES 5-8
  • Alternative lubricants of this invention are formulated using the respective additive packages of Examples A-D above as follows:
    Additive package 3.2% wt
    HiTEC® 614 Calcium Sulfonate 0.1% wt
    ETHYLFLO 170 PAO 80.7% wt
    ETHYLFLO 174 PAO 6.0% wt
    Diisodecyladipate 10.0% wt
  • EXAMPLE 9
  • A synthetic oil-based lubricating oil composition of this invention is formed by blending together the following components in the amounts specified:
       6.5% of the additive package of Example A, B, C or D;
       0.3% of HiTEC® 611 Calcium Sulfonate;
       39.9% of ETHYLFLO 168 poly-α-olefin oligomer oil (an 8 cSt base oil) (ETHYLFLO is a trademark of Ethyl Corporation);
       43.3% of a low chlorine version of ETHYLFLO 174 poly-α-olefin oligomer oil (a 40 cSt base oil); and
       10.0% of KETJENLUBE synthetic oil (KETJENLUBE is a trademark of Akzo Chemicals).
  • EXAMPLE 10
  • The ingredients listed below are pre-mixed in the relative proportions specified, heated to 60°C for 1.5 hours, and the resultant mixture is incorporated in an SAE 80W-90 synthetic fluid comprising 10.0% Ketjenlube 115 (Akzo Chemicals), 43.3% ETHYLFLO 174 PAO and 41.0% ETHYLFLO 168 PAO together with 0.2% w/w HiTEC® 611 Calcium Sulfonate at a concentration of 5.5% w/w.
    Sulfurized Isobutylene 3.9
    Octyl Amine 0.6
    Oleyl Amine 0.163
    Octanoic Acid 0.5
    2-Ethylhexyl-Acid Phosphate 0.196
    Copper Deactivator 0.07
    Antifoam 0.06
  • EXAMPLE 11
  • A gear oil additive concentrate of this invention is formed by heating at 50°C for one hour a mixture of sulfurized isobutylene, trihydrocarbyl ester of dithiophosphoric acid, octyl amine, bis-2-ethylhexylphosphate, oleylamine, alkyl acid phosphite, a friction modifier and a succinimide type dispersant. In the second stage of the procedure, oleic acid, antifoam agent, and process oil are added to the hot mixture produced in the first stage. The resultant concentrate is then allowed to cool to about 35°C, when metal deactivator and calcium sulfonate is added. The resultant concentrate contains (apart from amine tied up with phosphorus acids) approximately 21 mole % of sulphur per mole of amino nitrogen and approximately 0.56 chemical equivalent of weak acid (oleic acid) per equivalent of amino nitrogen. A gear oil is formed by blending this additive concentrate to a level of 6.5% w/w in an SAE 80W-90 synthetic fluid as in Example 10 above (equivalent to a concentration of 2.27 weight % of sulfurized isobutylene).
  • EXAMPLE 12
  • A mixture is formed from sulphurized isobutylene, oleylamine, octanoic acid, trihydrocarbyl dithiophosphate, a succinimide dispersant and a friction modifier in weight proportions of approximately 11.7:2.8:0.7:5.5:1:1 respectively. This mixture is heated at 60°C for one hour. To this hot mixture in a second stage are added octylamine, bis-2-ethylhexyl phosphate, an amine salt of a dihydrocarbyl thiophosphate and antifoam agent in weight proportions of approximately 0.2:0.4:3.3:0.2, respectively. Thereafter a mineral oil and a metal deactivator are added so that the resultant concentrate contains approximately 35% of the initial sulfurized isobutylene and approximately 18.3% of the mineral oil diluent. Excluding amine that is tied up with phosphorus acids, the additive concentrate contains approximately 18 mole % of sulfur per mole of amino nitrogen and approximately 0.6 equivalent of weak acid per equivalent of amino nitrogen. 3.25% of this additive package together with 0.3% of HiTEC® 611 calcium sulfonate is dissolved in a semi-synthetic fluid comprising 15% di(tridecyl)adipate, 25% ETHYLFLO 168 PAO, and 56.45% of mineral oil (Shell HVI 650b).
  • EXAMPLE 13
  • The procedure of Example 12 for producing the additive concentrate is repeated with the following modifications: the bis-2- ethylhexyl phosphate, the octylamine and the antifoam agent are included in the first stage, the oleyl amine, the dispersant and the friction modifier are introduced into the second stage reaction mixture, and the second stage reaction mixture is held at 50°C for 30 minutes. 6.5% of this additive package together with 0.5% of Amoco 421 magnesium sulfonate is dissolved in a fluid comprising a mixture of ETHYLFLO 168 PAO and mineral oil (Shell HVI 650b) to give a gear lubricant of SAE 80W-90 viscosity grade.
  • EXAMPLE 14
  • The procedure of Example 13 is repeated except that the first stage reaction mixture is heated to 50°C for 20 minutes and the second stage reaction mixture is held at 50°C for one hour. 6.5% of this additive package together with 0.25% of HiTEC®631 barium sulfonate is dissolved in a mixture of di(tridecyl)adipate (30%) and 63.25% mineral oil to give an SAE 80W-90 semi-synthetic gear lubricant.
  • EXAMPLE 15
  • The procedure of Example 12 for producing the additive concentrate is repeated except that the octylamine is added in the first stage reaction, the octanoic acid is added in the second stage reaction mixture, the first stage reaction mixture is maintained at 50°C for one hour, and the amine salt of a dihydrocarbyl thiophosphate is added in a final stage along with the mineral oil and metal deactivator. 3.0% of HiTEC® 611 high base sulfonate is stirred into the additive package which is then used to formulate synthetic and semi-synthetic lubricants suitable for use in manual automotive transmissions where a synchronization system is utilized.
  • EXAMPLE 16
  • The procedure of Example 12 for producing the additive concentrate is repeated with the following modifications: the octylamine and the trihydrocarbyl dithiophosphate are introduced into the first stage reaction mixture, and the octanoic acid is introduced into the second stage reaction mixture. This additive package is dissolved at 5.0% together with 0.2% of Lubrizol 6477 high base sulfonate in a synthetic fluid comprising a mixture of 25% of a poly-α-olefin made from dodecene, 44.8% of a poly-α-olefin made from decene (ETHYLFLO 168 PAO) and 25% of di(tridecyl)adipate.
  • EXAMPLE 17
  • A lubricating fluid of SAE 90 grade viscosity characteristics is blended with a commercially available additive package (HiTEC® 2375 additive: Ethyl Petroleum Additives, Ltd.; Ethyl Petroleum Additives, Inc.; Ethyl S.A.; Ethyl Canada Limited) in quantities such that the oil contains sulfurized isobutylene (2.27% w/w) and an alkylamine/alkylphosphate/alkylphosphite/alkylthiophosphate mixture (0.56%w/w). The oil also contains octanoic acid in a proportion such that there are approximately 136 moles of sulfur per mole of said acid. The sulfurized isobutylene itself is HiTEC® 309 additive. The alkylamine is entirely neutralized by the phosphorus acids present. 3.75% of this additive package is used in combination with 0.2% HiTEC® 631 barium sulfonate to formulate a semi-synthetic lubricant comprising 15% di(isodecyl)adipate, 30% ETHYLFLO 168 PAO and 56.05% Shell mineral oil (HVI 650b).
  • EXAMPLE 18
  • Stage 1. To a reaction vessel are charged 43.4 parts of sulfurized isobutylene, 4.44 parts of dibutyl hydrogen phosphite, 4.99 parts of C₁₂-C₁₄ tertiary alkyl primary amine (Primene 81R; Rohm & Haas Chemical Company), 1.16 parts of 2-ethylhexyl acid phosphate, and 2.56 parts of process oil. Throughout this addition, wherein the sulfurized isobutylene, phosphite and amines are added in the order named, the components of the reaction vessel are agitated. An exothermic reaction occurs on bringing the sulfurized isobutylene, phosphite and amines into contact with each other, and the rate of addition is controlled so that the temperature does not exceed 60°C. Concurrently a slight negative pressure is maintained on the reaction vessel in order to remove any volatiles produced during the exothermic reaction. The temperature of the reaction vessel is maintained at 55-60°C for 60 minutes while continuing the agitation. The mixture is then cooled to 40°C.
  • Stage 2. In a separate reactor, 0.69 part of M-544 defoamant (Monsanto Chemical Company), 0.73 part of caprylic acid, 0.50 part of a mixture of C₁₂ and C₁₄ tert-alkyl primary monoamines (Primene 81R), and 2.87 parts of process oil are agitated together for 15 minutes. The solution so formed is added to the Stage 1 product. Concurrently, added is 19.63 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl. Agitation is continued for 15 minutes, and the temperature is kept at 30-40°C. The pH of the resultant solution is approximately 6.9.
  • Stage 3. To the agitated solution of Stage 2 are added 3.0 parts of 2-tert-dodecyldithio-1,3,4-thiadiazole and 16.03 parts of process oil. Agitation is continued for 15 minutes while keeping the temperature at 30-40°C. The finished product is a bright clear amber liquid typically having a sulfur content of about 23.7% (wt) and a phosphorus content of about 2.35% (wt).
  • EXAMPLE 19
  • Stage 1. The procedure of Stage 1 of Example 18 is repeated using 34.97 parts of sulfurized isobutylene, 3.00 parts of dibutyl hydrogen phosphite, 5.60 parts of C₁₆₋₁₈ alkyl monoamine, 0.01 part of n-octyl amine, 0.98 part of 2-ethylhexyl acid phosphate, and 2.65 parts of process oil.
  • Stage 2. The product of Stage 1 is cooled to 40°C with continued agitation. Added to this product after the temperature reaches 40°C, is 16.61 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl.
  • Stage 3. In a separate reactor, 0.58 part of M-544 defoamant (Monsanto Chemical Company), 0.62 part of caprylic acid, 0.62 part of a C₃₆ dicarboxylic acid (formed by dimerization of oleic acid), and 2.65 parts of process oil are agitated together for 15 minutes. The resulting solution is added to the product from Stage 2. Agitation is continued for 15 minutes.
  • Stage 4. To the agitated mixture of Stage 3 are added 2.6 parts of 2-tert-dodecyldithio-1,3,4-thiadiazole and 2.65 parts of process oil. After these two components are added, 0.75 parts of dibutyl hydrogen phosphite is added to the mixture. Agitation is continued for 15 minutes.
  • Stage 5. To the agitated mixture of Stage 4 are added 23.07 parts of a mixture composed of 55% (wt) of a boronated succinimide (HiTEC® 648 additive; Ethyl Petroleum Additives, Inc.; Ethyl Petroleum Additives, Ltd.; Ethyl S.A.; Ethyl Canada Ltd.) and 45% (wt) of process oil, and 2.65 parts of additional process oil. Agitation is continued for 15 minutes to ensure complete blending of the components. The finished product is pumped through a filter. The product is a bright clear amber liquid typically containing, on a weight basis, about 19.3% sulfur, about 2.0% phosphorus, about 0.62% nitrogen, and about 0.16% boron. This concentrate is dissolved in a synthetic fluid at 3.5% together with 0.1% Amoco 421 magnesium sulfonate. In this case the synthetic fluid comprises 25% of a synthetic dibasic ester di(tridecyl)adipate and a 10 cSt (10 mm².s⁻¹) poly-α-olefin, ETHYLFLO 170 PAO.
  • EXAMPLE 20
  • Stage 1. The procedure of Stage 1 of Example 18 is repeated using 31.26 parts of sulfurized isobutylene, 2.44 parts of dibutyl hydrogen phosphite, 3.18 parts of C₁₆₋₁₈ alkyl monoamine, 0.63 part of n-octyl amine, 0.80 part of 2-ethylhexyl acid phosphate, and 5.19 parts of process oil. The pH of the resulting mixture is approximately 7.0.
  • Stage 2. In a separate reactor, 0.47 part of M-544 defoamant (Monsanto Chemical Company), 0.51 part of caprylic acid, 0.51 part of C₃₆ dicarboxylic acid (formed by dimerization of oleic acid), and 5.19 parts of process oil are agitated together for 15 minutes. The solution so formed is added to the Stage 1 product. Concurrently, added is 10.66 parts of a product formed by reaction of dicyclopentadiene with dithiophosphoric acid-0,0-dialkyl ester in which on a molar basis 40% of the alkyl groups are isopropyl, 40% are isobutyl and 20% are 2-ethylhexyl. Agitation is continued for 60 minutes, and the temperature is kept at 40°C.
  • Stage 3. To the agitated solution of Stage 2 is added 2.14 parts of 2,5-dimethylthio-1,3,4-thiadiazole and 5.19 parts of process oil. Then 0.61 part of dibutyl hydrogen phosphite is added to the mixture. Agitation is continued for 15 minutes.
  • Stage 4. To the agitated solution from Stage 3 are added 10.32 parts of a mixture composed of 55% (wt) of a boronated succinimide (HiTEC® 648 additive; Ethyl Petroleum Additives, Inc.; Ethyl Petroleum Additives, Ltd.; Ethyl S.A.; Ethyl Canada Ltd.) and 45.% (wt) of process oil, 6.24 parts of alkenylsuccinimide (formed from ammonia and alkenyl succinic anhydride produced from a mixture of olefins made by isomerizing a 1-olefin mixture containing 49% C₂₀, 42% C₂₂, and 8% C₂₄ 1-olefins, and 14.66 parts of additional process oil. Agitation is continued for 15 minutes to ensure complete blending of the components. The finished product is pumped through a filter. The product is a bright clear amber liquid typically containing, on a weight basis, about 17.5% sulfur, and about 1.6% phosphorus. This product is dissolved in a fluid comprising 0.5% calcium sulfonate (HiTEC® 611 additive), 27% Lubrizol 3174 shear stable viscosity index improver, 40% of a synthetic ester di(isodecyl)adipate and 32.5% of ETHYLFLO 168 PAO.
  • EXAMPLE E
  • An additive concentrate is prepared as follows:
  • 14 parts by weight of trihydrocarbyl dithiophosphate [where two of the substituents are a mixture of isopropyl, n-butyl and 2-ethylhexyl (in a 40:40:20 ratio) and the third substituent is derived from dicyclopentadiene] is stirred at approximately 30°C with 38 parts of sulfurized isobutylene, 1.75 parts 2-ethylhexyl acid phosphate, and 4.76 parts of dibutyl hydrogen phosphite.
  • 6 parts of a tertiary alkyl primary amine (PRIMENE 81R) is added and allowed to react. After approximately 30 minutes a polyisobutylene substituted succinimide dispersant at 2.42 parts by weight and a further 4.9 parts of PRIMENE 81R is added and the resultant mixture stirred at about 55°C for one hour.
  • 0.57 parts of polyalkylacrylate antifoamant, 4.31 parts of oleic acid and 5.63 parts of mineral oil are stirred into the mixture which is subsequently allowed to cool to below 40°C.
  • 1.8 parts of a thiadiazole (HiTEC® 314 additive) is then added to the mixture which is allowed to cool to room temperature.
  • EXAMPLE 21
  • Into the additive concentrate prepared as in Example E above are stirred 3.15 parts of HiTEC® 611 calcium sulfonate and 11.85 parts of mineral oil to give an additive package suitable for formulating gear oils.
  • EXAMPLE 22
  • Into the additive concentrate prepared as in Example E above is stirred 15 parts of HiTEC® 614 calcium sulfonate to give an additive concentrate.
  • EXAMPLE 23
  • Into the additive concentrate prepared as in Example E above are stirred 3.0 parts of Amoco 421 magnesium sulfonate and 12.0 parts of mineral oil.
  • EXAMPLE 24
  • Into the additive concentrate prepared as in Example E above are blended 1.0 part of sodium alkyl benzene sulfonate, 2.0 parts of HiTEC® 611 calcium sulfonate and 12.0 parts of mineral oil.
  • EXAMPLE 25
  • The following Table gives examples of gear oil formulations containing the respective additive packages described in Examples 21-24 above.
    (I) (II) (III) (IV) (V)
    Additive Package (Ex. 21, 22, 23 or 24 3.2 6.5 7.5 7.5 3.2
    Diisodecyladipate 10 10 10.5 10.5 --
    ETHYLFLO 170 PAO 80.8 32.2 - - -
    ETHYLFLO 168 PAO - - 32.5 32.0 66.8
    ETHYLFLO 174 PAO 6 51.3 49.5 - -
    KETJENLUBE 115 - - - - 10.0
    Shell HVI650b mineral oil - - - 50.0 20.0
  • EXAMPLE F
  • A chemical composition is prepared as follows:
  • 6.26 parts of a trihydrocarbyl dithiophosphate [where two of the substituents are a mixture of isopropyl, n-butyl and 2-ethylhexyl (in a 40:40:20 ratio) and the third substituent is derived from dicyclopentadiene] is stirred with 44 parts of sulfurized isobutylene, 5.33 parts dibutylhydrogen phosphite and 1.94 parts of 2-ethylhexylacid phosphate for 10 minutes at about 30°C. To this mixture is added 0.6 parts of octylamine followed by a mixture of 6.0 parts PRIMENE 81R amine and 1.2 parts oleylamine. The resulting mixture is then heated to about 55°C for about 1 hour after which time heating is terminated and the following acidic mixture is added:
  • ACIDIC MIXTURE
  •    5 parts mineral oil
       2.2 parts oleic acid
       0.5 part polyalkylacrylate antifoamant
       0.3 part caprylic acid
       0.116 part TOLAD 9308 (Petrolite)
       0.106 part polyethylene/propylene block copolymer
       0.777 part TOLAD 370 (Petrolite)
    After cooling and stirring to below 40°C, 9.33 parts of Amoco 9250, 1.2 parts of a thiadiazole (HiTEC 314 additive) and 15.781 parts mineral oil are added.
  • EXAMPLE 26
  • The composition formed as described in Example F above is mixed 50:50 by weight with calcium sulfonate (HiTEC 611 additive and used in formulating transmission oils as described in Example 27 below.
  • EXAMPLE 27
  • (I) (II) (III) (IV) (V) (VI)
    Composition of Example 26 0.2 1.0 0.3 0.2 0.9 1.0
    Composition of Example F 3.75 7.5 -- -- -- --
    Anglamol 99 (Low Chlorine) -- -- 3.9 -- -- --
    Anglamol 9000 -- -- -- -- 7.0 --
    Mobilab G521T -- -- -- -- -- 5.0
    Diisodecyladipate 10.0 20.0 20.0 20.0 25.0 20.0
    ETHYLFLO 168 PAO -- 11.5 -- 10.0 17.1 --
    ETHYLFLO 170 PAO 80.0 -- 70.0 -- -- 74.0
    ETHYLFLO 174 PAO 6.05 -- 5.8 -- -- --
    Mineral oil (Shell HV1650b) -- 60 -- 64.8 50 --
  • EXAMPLE 28
  • A semi-synthetic gear fluid of this invention is formed from Anglamol 99 gear additive package at 3.9% and barium sulfonate (HiTEC 631 additive) at 0.2% in a mixture of 10% diisodecyl adipate, 25% hydrotreated mineral oil (Shell XHVI 5.2) and 60.9% mineral oil (Shell HVI 650b).
  • EXAMPLE 29
  • Blended together are Anglamol 6004A gear additive package at 6.5%, HiTEC 614® calcium sulfonate at 0.5%, diisodecyladipate at 10%, ETHYLFLO 174 PAO at 6.0% and ETHYLFLO 170 PAO at 77% to give an SAE 80W fluid of this invention.
  • EXAMPLE 30
  • With a mixture of 33.2% of diisodecyladipate and 60% of ETHYLFLO 174 PAO are blended 6.6% Mobilad G521T gear additive package and 0.2% Amoco 421 magnesium sulfonate to give a gear lubricant of the invention.
  • EXAMPLE 31
  • A semi-synthetic gear lubricant of the invention is formed when 8.0% of Anglamol 6043U gear additive is blended with 0.2% HiTEC 631 barium sulfonate, 35% of di(tridecyl) adipate and 56.8% of mineral oil (Shell HVI 650b).
  • EXAMPLE 32
  • Blended together are 6.5% of a low chlorine version of Anglamol 99 gear additive, 0.5% HiTEC 631 barium sulfonate, 1.5% HiTEC 623 pour point depressant, 65% mineral oil (Shell HVI 650b) and 26.5% of ETHYLFLO 168 PAO to give a semisynthetic gear lubricant of the invention.
  • EXAMPLE 33
  • With a mixture of 7.0% Anglamol 9000 gear additive, 0.1% HiTEC 611 calcium sulfonate and 1.0% HiTEC 623 pour point depressant are blended 33% diisodecyladipate and 58.9% Shell HVI 650b mineral oil to give a semi-synthetic gear fluid of the invention.
  • EXAMPLE 34
  • A semi-synthetic gear lubricant of the invention is formed when 8.0% of Anglamol 6043U gear additive is blended with 0.1% potassium alkylbenzene sulfonate, 0.1% HiTEC 611 calcium sulfonate, 35% di(tridecyl)adipate and 56.8% of mineral oil.
  • EXAMPLE 35
  • Blended together are 6.5% of a low chlorine version of Anglamol 99 gear additive, 0.2% sodium alkylbenzene sulfonate, 0.2% Amoco 421 magnesium sulfonate, 0.2% HiTEC 614 calcium sulfonate, 1.5% HiTEC 623 pour point depressant, 65% mineral oil (Shell HVI 650b) and 26.5% of diisodecyladipate to give a lubricant of the invention suitable for use in manual transmissions and final drives of certain motor vehicles.
  • It will of course be appreciated by those skilled in the art that the various above three Anglamol products (The Lubrizol Corporation) and the above Mobilad product (Mobil Chemical Company) are all gear oil additive packages based on use of phosphorus- and sulfur-containing antiwear and/or extreme pressure additive componentry.
  • The performance improvements achievable by the practice of this invention are illustrated, but by no means limited, by the results of various ZF.Synchronizer tests conducted as described hereinabove. Table I summarizes the results of tests in which a gear additive package (HiTEC® 380 additive; Ethyl Petroleum Additives, Ltd., Bracknell, England) was blended into various base oils at API-GL4 dosage levels. In Table I all percentages are by weight, and:
  • PAO (I)
    is ETHYLFLO 170 PAO (Ethyl Corporation), a hydrogenerated poly-α-olefin having a kinematic viscosity at 100°C of approximately 9.6 mm².s⁻¹ (cSt);
    ESTER
    is diisodecyl adipate;
    MIN. OIL
    is Shell HVI 115; and
    PAO (II)
    is ETHYLFLO 174 PAO (Ethyl Corporation), a hydrogenated poly-α-olefin having a kinematic viscosity at 100°C of approximately 40 mm².s⁻¹ (cSt).
  • The above Shell HVI 115 mineral oil was a solvent neutral oil having a kinematic viscosity of 9 mm².s⁻¹ (cSt) at 100°C containing 1.0 HiTEC® 623 pour point depressant. The first seven tests in Table I (i.e., Run Nos. 1-7) used SAE 80W viscosity grade formulations. Run Nos. 1-7 are comparative tests as none of these formulations contained a sulfonate additive. However, Run No. 8 used a formulation containing 0.5 wt% of HiTEC® 611 additive, an overbased calcium alkylbenzene sulfonate having a nominal TBN of 300 available commercially from Ethyl Petroleum Additives, Inc. and Ethyl Petroleum Additives, Ltd. The HiTEC 611 additive contains approximately 44% diluent oil. The formulation of Run No. 8 is an SAE 90 grade formulation useful as a total driveline fluid suitable for use in final drives such as hypoid differentials, as well as gear boxes. TABLE I
    Run No. % HiTEC 380 % PAO (I) % ESTER % MIN. OIL %PAO (II) ZF RESULTS
    1 3.2 -- -- 96.8 -- PASS
    2 3.2 96.8 -- -- -- FAIL
    3 3.2 86.8 10 -- -- FAIL
    4 6.5 86.8 10 -- -- FAIL
    5 3.2 71.8 25 -- -- FAIL
    6 3.2 71.8 25 -- -- FAIL
    7 3.2 36.8 -- 60 -- FAIL
    8 6.5 32.2 10 -- 50.8 PASS
  • It will be seen by comparing the results of Run Nos. 2-7 with Run No. 1 that the fluids containing the synthetic oils failed the tests whereas the mineral oil based fluid passed. Run No. 8 shows that inclusion in the synthetic oil based fluid of a small amount of a metal sulfonate pursuant to this invention improved the frictional properties of the blend to such an extent that it passed the test.
  • Table II summarizes the results of additional ZF.Synchronizer tests which demonstrate the practice and advantages of this invention.
  • Run Nos. 11-14 represent the practice of this invention as these gear oils contained, respectively, 2.0, 1.0, 0.2 and 0.1% of a metal sulfonate (HiTEC® 611 additive). In Run No. 15 the gear oil contained, for comparative purposes, 1.0% of an alkenyl succinimide friction modifier of the type described in EP 20,037. The oil of Run No. 16 contained 3.5% of a polyisobutenyl succinimide ashless dispersant (HiTEC® 646 additive; Ethyl Petroleum Additives, Inc.; Ethyl Petroleum Additives, Ltd. and their affiliated companies). The foregoing percentages are on an "as received basis" and thus include solvent oils. The succinimide friction modifier of Run No. 15 contained no diluent. As in the case of Table I, all percentages are by weight, also "PAO (I)", "PAO (II)", and "ESTER" have the same meanings as in Table I. TABLE II
    Run No. % HiTEC 380 % PAO (I) % PAO (II) % ESTER ZF RESULT
    9 3.2 46.8 25.0 25 FAIL
    10 6.5 80.0 3.5 10 FAIL
    11 3.2 78.8 6.0 10 PASS
    12 3.2 79.8 6.0 10 PASS
    13 3.2 80.6 6.0 10 PASS
    14 3.2 80.7 6.0 10 PASS
    15 3.2 79.8 6.0 10 FAIL
    16 3.2 77.3 6.0 10 FAIL
  • As used in the foregoing description, the term "oil-soluble" is used in the sense that the component in question has sufficient solubility in the selected base oil in order to dissolve therein at ordinary temperatures to a concentration at least equivalent to the minimum concentration specified herein for use of such component. Preferably, however, the solubility of such component in the selected base oil will be in excess of such minimum concentration, although there is no requirement that the component be soluble in the base oil in all proportions. As is well known to those skilled in the art, certain useful additives do not completely dissolve in base oils but rather are used in the form of stable suspensions or dispersions. Additives of this type can be employed in the compositions of this invention, provided they do not significantly interfere with the performance or usefulness of the composition in which they are employed.

Claims (10)

  1. A gear oil lubricant having a kinematic viscosity at 100°C in the range of 4 to 32 mm².s⁻¹ (cSt), and comprising:
    a) a base oil having at least 25% by weight of (i) hydrogenated poly-alpha-olefin oligomer oil or (ii) synthetic ester oil, or (iii) a combination of (i) and (ii);
    b) an amount of a gear oil additive package such that the gear oil lubricant satisfies or exceeds the specifications for GL4 service; and
    c) an amount in the range of 0.01 to 2 wt % based on the total weight of the lubricant of at least one alkali or alkaline earth metal salt of an oil-soluble sulfonic acid, the amount of said metal salt used being sufficient to improve the friction properties of the lubricant for use in manual transmissions, particularly those of the synchronizer type;
    said lubricant containing at most, if any, 100 ppm of metal as one or more metal-containing additive components other than said metal salt, and having on a weight basis a boron content, if any, of not more than 1,000 ppm.
  2. A lubricant composition according to Claim 1 wherein said component c) is a calcium salt of an oil-soluble alkylbenzene sulfonic acid.
  3. A lubricant composition according to Claim 1 wherein said component c) is an overbased salt of the sulfonic acid.
  4. A lubricant composition according to Claim 1 wherein said component a) is at least 50% by weight of hydrogenated poly-alpha-olefin oligomer oil.
  5. A gear oil additive package (concentrate) which comprises:
    a) at least one oil-soluble ashless dispersant, selected from succinimide ashless dispersants and/or succinic ester-amide ashless dispersants, and Mannich base ashless dispersants;
    b) at least one oil-soluble metal-free sulfur-containing antiwear and/or extreme pressure agent;
    c) at least one oil-soluble metal-free phosphorus-containing antiwear and/or extreme pressure agent; and
    d) at least one alkali or alkaline metal salt of an oil-soluble sulfonic acid in an amount such that a lubricant composition formed by blending the additive package in a base oil having a kinematic viscosity in the range of 4 to 32 cSt at 100°C and composed of at least 25% by weight of (i) hydrogenated polyalpha-olefin oligomer oil or (ii) synthetic ester oil, or (iii) a combination of (i) and (ii) to form a lubricant containing from 0.01 to 2 wt % of said metal salt, provides a lubricant composition that:
    A) satisfies or exceeds the specifications for API GL4 service;
    B) contains at most 100 ppm, if any, of metal apart from the metal of said metal salt; and
    C) has a boron content, if any, of not more than 1,000 ppm.
  6. A gear oil additive package according to Claim 5 wherein said metal salt is a calcium salt of an oil-soluble alkylbenzene sulfonic acid.
  7. A gear oil additive package according to Claim 5 wherein said metal salt is an overbased salt of the sulfonic acid.
  8. A gear oil additive package according to Claim 5 further characterized by having a total halogen content, if any, of not more than 1000 ppm on a weight basis.
  9. A gear oil additive package according to Claim 8 wherein said total halogen content, if any, does not exceed 250 ppm on a weight basis.
  10. A method of beneficially modifying the frictional characteristics of a low-friction synthetic lubricant composition containing at least 25% by weight of (i) hydrogenated poly-alpha-olefin oligomer oil or (ii) synthetic ester oil or (iii) a combination of (i) and (ii) and a gear oil additive package such that the lubricant composition satisfies or exceeds the specifications for API-GL4 service, but does not exhibit satisfactory friction pro-perties for use in manual transmissions, particularly those of the synchronizer type, said method comprising including in such lubricant composition an amount in the range of 0.01 to 2 wt % based on the total weight of the lubricant of at least one alkali or alkaline earth metal salt of an oil-soluble sulfonic acid such that the friction properties of said lubricant are improved for use in manual transmissions of the synchronizer type.
EP93305125A 1992-07-09 1993-06-30 Friction modification of synthetic gear oils Revoked EP0578435B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US91120392A 1992-07-09 1992-07-09
US911203 1992-07-09

Publications (2)

Publication Number Publication Date
EP0578435A1 true EP0578435A1 (en) 1994-01-12
EP0578435B1 EP0578435B1 (en) 1997-10-15

Family

ID=25429898

Family Applications (1)

Application Number Title Priority Date Filing Date
EP93305125A Revoked EP0578435B1 (en) 1992-07-09 1993-06-30 Friction modification of synthetic gear oils

Country Status (4)

Country Link
EP (1) EP0578435B1 (en)
JP (1) JPH06179887A (en)
CA (1) CA2099314A1 (en)
DE (1) DE69314554T2 (en)

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0692012A1 (en) * 1993-04-01 1996-01-17 Ethyl Corporation Gear oil compositions
EP0747465A2 (en) * 1995-06-07 1996-12-11 Ethyl Petroleum Additives Limited Use of transmission and gear oil lubricants having enhanced friction properties
EP0747464A1 (en) * 1995-06-09 1996-12-11 The Lubrizol Corporation A composition for providing anti-shudder friction durability performance for automatic transmissions
EP0767236A1 (en) * 1995-10-04 1997-04-09 Ethyl Petroleum Additives Limited Friction modification of synthetic gear oils
US5883057A (en) * 1996-01-16 1999-03-16 The Lubrizol Corporation Lubricating compositions
WO1999016849A1 (en) * 1997-10-01 1999-04-08 Unichema Chemie B.V. Complex esters, formulations comprising these esters and use thereof
WO1999018175A1 (en) * 1997-10-03 1999-04-15 Infineum Usa Lp Lubricating compositions
EP1186647A1 (en) * 2000-09-01 2002-03-13 Minebea Co., Ltd. Moulded plastic products with anticorrosive lubricating coating
US6489271B1 (en) 1994-08-03 2002-12-03 The Lubrizol Corporation Combination of a sulfur compound and specific phosphorus compounds and their use in lubricating compositions, concentrates and greases
SG94669A1 (en) * 1995-08-11 2003-03-18 Lubrizol Corp Combination of a sulfur compound and specific phosphorus compounds and their use in lubricating compositions, concentrates and greases
EP1344814A1 (en) * 2002-03-15 2003-09-17 Infineum International Limited Power transmission fluids of improved anti-shudder properties
EP1382660A1 (en) * 2002-07-18 2004-01-21 Primrose Oil Company Synthetic lubricant oil compositions for internal combustion engines
WO2004106763A2 (en) * 2003-05-30 2004-12-09 Volkswagen Aktiengesellschaft Double-clutch drive
US6962895B2 (en) 1996-01-16 2005-11-08 The Lubrizol Corporation Lubricating compositions
EP1785476A1 (en) * 2005-11-09 2007-05-16 Afton Chemical Corporation Lubricant composition
EP1785470A3 (en) * 2005-11-09 2007-08-22 Afton Chemical Corporation Composition comprising a sulfur-containing, phosphorus-containing compound, and/or its salt, and uses thereof
EP1832646A1 (en) * 2006-03-09 2007-09-12 Afton Chemical Corporation Lubricant composition
WO2008081287A2 (en) * 2006-12-27 2008-07-10 Shell Internationale Research Maatschappij B.V. Lubricating oil composition
US7928260B2 (en) 2005-11-09 2011-04-19 Afton Chemical Corporation Salt of a sulfur-containing, phosphorus-containing compound, and methods thereof
RU2456335C1 (en) * 2011-06-09 2012-07-20 Открытое акционерное общество "Всероссийский научно-исследовательский институт по переработке нефти" (ОАО "ВНИИ НП") Engine oil
WO2013148146A1 (en) 2012-03-26 2013-10-03 The Lubrizol Corporation Manual transmission lubricants with improved synchromesh performance
WO2013148171A1 (en) 2012-03-26 2013-10-03 The Lubrizol Corporation Manual transmission lubricants with improved synchromesh performance
WO2014088782A1 (en) * 2012-12-03 2014-06-12 The Lubrizol Corporation Industrial gear oils imparting reduced gearbox operating temperatures
RU2708887C1 (en) * 2019-02-28 2019-12-12 Публичное акционерное общество "Нефтяная компания "Роснефть" (ПАО "НК "Роснефть") Composition and method of obtaining a package of additives for hydraulic oils and multigrade hydraulic oil containing
CN111356754A (en) * 2017-08-29 2020-06-30 巴斯夫欧洲公司 Transmission lubricant composition

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002285184A (en) * 2001-02-20 2002-10-03 Ethyl Corp Low phosphorus containing clean gear oil formulation
JP4808027B2 (en) * 2003-02-07 2011-11-02 Jx日鉱日石エネルギー株式会社 Lubricating oil composition for transmission
JP4328120B2 (en) * 2003-03-31 2009-09-09 住友重機械工業株式会社 Swing intermeshing planetary gear device and method for improving durability thereof
US8034754B2 (en) 2005-03-31 2011-10-11 The Lubrizol Corporation Fluids for enhanced gear protection
US20070142237A1 (en) * 2005-11-09 2007-06-21 Degonia David J Lubricant composition
US20090093384A1 (en) * 2007-10-03 2009-04-09 The Lubrizol Corporation Lubricants That Decrease Micropitting for Industrial Gears
WO2012066575A1 (en) 2010-11-19 2012-05-24 Indian Oil Corporation Ltd. A high performance gearbox lubricant with enhanced drain interval for heavy duty commercial vehicles and a process for producing the same
MX2013005269A (en) * 2010-11-19 2013-06-03 Chevron Usa Inc Lubricant for percussion equipment.

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2442265A1 (en) * 1978-11-22 1980-06-20 Exxon Research Engineering Co LUBRICATING OIL COMPOSITION FOR AUTOMATIC TRANSMISSION
EP0237804A2 (en) * 1986-02-19 1987-09-23 Nippon Oil Co. Ltd. Oil composition for manual transmission
WO1988005810A1 (en) * 1987-01-30 1988-08-11 The Lubrizol Corporation Gear lubricant composition
EP0407124A1 (en) * 1989-07-07 1991-01-09 Tonen Corporation Lubricating oil composition
EP0399764B1 (en) * 1989-05-22 1992-03-25 Ethyl Petroleum Additives Limited Lubricant compositions
EP0480644A1 (en) * 1990-10-10 1992-04-15 Ethyl Petroleum Additives, Inc. Ashless or low-ash synthetic base compositions and additives therefor
EP0531585A1 (en) * 1991-09-09 1993-03-17 Ethyl Petroleum Additives Limited Oil additive concentrates and lubricants of enhanced performance capabilities

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IN169147B (en) * 1986-04-04 1991-09-07 Lubrizol Corp
SG52521A1 (en) * 1990-01-05 1998-09-28 Lubrizol Corp Universal driveline fluid

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2442265A1 (en) * 1978-11-22 1980-06-20 Exxon Research Engineering Co LUBRICATING OIL COMPOSITION FOR AUTOMATIC TRANSMISSION
EP0237804A2 (en) * 1986-02-19 1987-09-23 Nippon Oil Co. Ltd. Oil composition for manual transmission
WO1988005810A1 (en) * 1987-01-30 1988-08-11 The Lubrizol Corporation Gear lubricant composition
EP0399764B1 (en) * 1989-05-22 1992-03-25 Ethyl Petroleum Additives Limited Lubricant compositions
EP0407124A1 (en) * 1989-07-07 1991-01-09 Tonen Corporation Lubricating oil composition
EP0480644A1 (en) * 1990-10-10 1992-04-15 Ethyl Petroleum Additives, Inc. Ashless or low-ash synthetic base compositions and additives therefor
EP0531585A1 (en) * 1991-09-09 1993-03-17 Ethyl Petroleum Additives Limited Oil additive concentrates and lubricants of enhanced performance capabilities

Cited By (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0692012A4 (en) * 1993-04-01 1996-01-24
EP0692012A1 (en) * 1993-04-01 1996-01-17 Ethyl Corporation Gear oil compositions
US5691283A (en) * 1994-03-01 1997-11-25 Ethyl Petroleum Additives Limited Use of transmission and gear oil lubricants having enhanced friction properties
US6489271B1 (en) 1994-08-03 2002-12-03 The Lubrizol Corporation Combination of a sulfur compound and specific phosphorus compounds and their use in lubricating compositions, concentrates and greases
EP0747465A2 (en) * 1995-06-07 1996-12-11 Ethyl Petroleum Additives Limited Use of transmission and gear oil lubricants having enhanced friction properties
EP0747465A3 (en) * 1995-06-07 1997-01-15 Ethyl Petroleum Additives Limited Use of transmission and gear oil lubricants having enhanced friction properties
AU711001B2 (en) * 1995-06-09 1999-10-07 Lubrizol Corporation, The A composition for providing anti-shudder friction durability performance for automatic transmissions
EP0747464A1 (en) * 1995-06-09 1996-12-11 The Lubrizol Corporation A composition for providing anti-shudder friction durability performance for automatic transmissions
US5858929A (en) * 1995-06-09 1999-01-12 The Lubrizol Corporation Composition for providing anti-shudder friction durability performance for automatic transmissions
AU711001C (en) * 1995-06-09 2002-10-17 Lubrizol Corporation, The A composition for providing anti-shudder friction durability performance for automatic transmissions
SG94669A1 (en) * 1995-08-11 2003-03-18 Lubrizol Corp Combination of a sulfur compound and specific phosphorus compounds and their use in lubricating compositions, concentrates and greases
EP0767236A1 (en) * 1995-10-04 1997-04-09 Ethyl Petroleum Additives Limited Friction modification of synthetic gear oils
US5883057A (en) * 1996-01-16 1999-03-16 The Lubrizol Corporation Lubricating compositions
US6962895B2 (en) 1996-01-16 2005-11-08 The Lubrizol Corporation Lubricating compositions
US6462001B1 (en) 1997-10-01 2002-10-08 Unichema Chemie Bv Complex esters, formulations comprising these esters and use thereof
WO1999016849A1 (en) * 1997-10-01 1999-04-08 Unichema Chemie B.V. Complex esters, formulations comprising these esters and use thereof
MY119806A (en) * 1997-10-01 2005-07-29 Unichema Chemie Bv Esters, formulations comprising these esters and use thereof
WO1999018175A1 (en) * 1997-10-03 1999-04-15 Infineum Usa Lp Lubricating compositions
US6844301B2 (en) 1997-10-03 2005-01-18 Infineum Usa Lp Lubricating compositions
EP1186647A1 (en) * 2000-09-01 2002-03-13 Minebea Co., Ltd. Moulded plastic products with anticorrosive lubricating coating
US6703354B2 (en) 2000-09-01 2004-03-09 Minebea Co., Ltd. Anticorrosive lubricant composition for molded plastic products and molded plastic products with same applied thereto
EP1344814A1 (en) * 2002-03-15 2003-09-17 Infineum International Limited Power transmission fluids of improved anti-shudder properties
EP1382660A1 (en) * 2002-07-18 2004-01-21 Primrose Oil Company Synthetic lubricant oil compositions for internal combustion engines
WO2004106763A2 (en) * 2003-05-30 2004-12-09 Volkswagen Aktiengesellschaft Double-clutch drive
WO2004106763A3 (en) * 2003-05-30 2005-05-19 Volkswagen Ag Double-clutch drive
EP2019225A1 (en) 2003-05-30 2009-01-28 Volkswagen Aktiengesellschaft Double clutch gearbox
US7928260B2 (en) 2005-11-09 2011-04-19 Afton Chemical Corporation Salt of a sulfur-containing, phosphorus-containing compound, and methods thereof
EP1785476A1 (en) * 2005-11-09 2007-05-16 Afton Chemical Corporation Lubricant composition
EP1785470A3 (en) * 2005-11-09 2007-08-22 Afton Chemical Corporation Composition comprising a sulfur-containing, phosphorus-containing compound, and/or its salt, and uses thereof
US8299003B2 (en) 2005-11-09 2012-10-30 Afton Chemical Corporation Composition comprising a sulfur-containing, phosphorus-containing compound, and/or its salt, and uses thereof
EP1832646A1 (en) * 2006-03-09 2007-09-12 Afton Chemical Corporation Lubricant composition
US8168573B2 (en) 2006-12-27 2012-05-01 Shell Oil Company Lubricating oil composition
WO2008081287A3 (en) * 2006-12-27 2008-08-28 Shell Int Research Lubricating oil composition
WO2008081287A2 (en) * 2006-12-27 2008-07-10 Shell Internationale Research Maatschappij B.V. Lubricating oil composition
RU2456335C1 (en) * 2011-06-09 2012-07-20 Открытое акционерное общество "Всероссийский научно-исследовательский институт по переработке нефти" (ОАО "ВНИИ НП") Engine oil
WO2013148146A1 (en) 2012-03-26 2013-10-03 The Lubrizol Corporation Manual transmission lubricants with improved synchromesh performance
WO2013148171A1 (en) 2012-03-26 2013-10-03 The Lubrizol Corporation Manual transmission lubricants with improved synchromesh performance
WO2014088782A1 (en) * 2012-12-03 2014-06-12 The Lubrizol Corporation Industrial gear oils imparting reduced gearbox operating temperatures
CN111356754A (en) * 2017-08-29 2020-06-30 巴斯夫欧洲公司 Transmission lubricant composition
EP3676358A4 (en) * 2017-08-29 2021-05-12 Basf Se Transmission lubricant composition
RU2708887C1 (en) * 2019-02-28 2019-12-12 Публичное акционерное общество "Нефтяная компания "Роснефть" (ПАО "НК "Роснефть") Composition and method of obtaining a package of additives for hydraulic oils and multigrade hydraulic oil containing

Also Published As

Publication number Publication date
CA2099314A1 (en) 1994-01-10
DE69314554T2 (en) 1998-02-19
EP0578435B1 (en) 1997-10-15
JPH06179887A (en) 1994-06-28
DE69314554D1 (en) 1997-11-20

Similar Documents

Publication Publication Date Title
EP0578435B1 (en) Friction modification of synthetic gear oils
EP0747465B1 (en) Use of transmission and gear oil lubricants having enhanced friction properties
JP4101310B2 (en) Gear oil lubricant with enhanced friction performance
AU702057B2 (en) Lubricant compositions to reduce noise in a push belt continuous variable transmission
JP4856305B2 (en) Engine oil composition
CA2159120A1 (en) Gear oil compositions
JPH09194870A (en) Lubricating composition
JP2020502350A (en) Fluorinated polyacrylate antifoam components for lubricating compositions
JPH09132790A (en) Gear oil composition
EP0767236B1 (en) Friction modification of synthetic gear oils
JP4409055B2 (en) Gear oil composition
EP0244043B1 (en) Lubricating grease
JP2972386B2 (en) Antioxidant composition
JP4307575B2 (en) Lubricating oil composition
EP3464525B1 (en) Seal swell agents for lubricating compositions
EP3380592B1 (en) Seal swell agents for lubricating compositions
EP0889112A1 (en) Lubricating oil composition for automatic transmissions
CN109862921B (en) Novel amino diphosphonate antiwear additive
CN114945652A (en) Friction modifier compounds and related compositions and methods

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE ES FR GB IT

RIN1 Information on inventor provided before grant (corrected)

Inventor name: CAMPBELL, DONALD GALE

Inventor name: MACPHERSON, IAN

17P Request for examination filed

Effective date: 19940314

17Q First examination report despatched

Effective date: 19951025

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE DE ES FR GB IT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 19971015

REF Corresponds to:

Ref document number: 69314554

Country of ref document: DE

Date of ref document: 19971120

ET Fr: translation filed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19980116

PLBQ Unpublished change to opponent data

Free format text: ORIGINAL CODE: EPIDOS OPPO

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

26 Opposition filed

Opponent name: THE LUBRIZOL CORPORATION

Effective date: 19980715

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19990601

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19990602

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19990603

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 19990624

Year of fee payment: 7

RDAH Patent revoked

Free format text: ORIGINAL CODE: EPIDOS REVO

RDAG Patent revoked

Free format text: ORIGINAL CODE: 0009271

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: PATENT REVOKED

27W Patent revoked

Effective date: 19991103

GBPR Gb: patent revoked under art. 102 of the ep convention designating the uk as contracting state

Free format text: 991103