GB718714A - Lubricating oil compositions - Google Patents

Lubricating oil compositions

Info

Publication number
GB718714A
GB718714A GB19393/51A GB1939351A GB718714A GB 718714 A GB718714 A GB 718714A GB 19393/51 A GB19393/51 A GB 19393/51A GB 1939351 A GB1939351 A GB 1939351A GB 718714 A GB718714 A GB 718714A
Authority
GB
United Kingdom
Prior art keywords
calcium
sulphonate
benzene
oil
lubricating oil
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB19393/51A
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.)
California Research LLC
Original Assignee
California Research LLC
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
Application filed by California Research LLC filed Critical California Research LLC
Publication of GB718714A publication Critical patent/GB718714A/en
Expired legal-status Critical Current

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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
    • 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
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    • 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
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/062Oxides; Hydroxides; Carbonates or bicarbonates
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/063Peroxides
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    • 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
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    • 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
    • C10M2205/026Butene
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
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    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027Neutral salts thereof
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    • 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
    • C10M2207/028Overbased salts thereof
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    • 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
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    • 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
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    • C10M2207/16Naphthenic acids
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    • 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
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    • 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
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    • 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
    • C10M2209/086Macromolecular 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 polycarboxylic, e.g. maleic acid
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    • 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
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    • 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
    • C10M2209/105Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
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    • 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
    • C10M2209/108Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
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    • 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
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2215/065Phenyl-Naphthyl amines
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    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2215/068Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings having amino groups bound to polycyclic aromatic ring systems, i.e. systems with three or more condensed rings
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
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    • C10M2223/04Phosphate esters
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    • 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
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    • C10M2223/041Triaryl phosphates
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    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
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    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
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    • C10M2223/047Thioderivatives not containing metallic elements
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/06Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
    • C10M2223/065Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds containing sulfur
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    • 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
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    • C10M2225/00Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions
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    • C10N2010/00Metal present as such or in compounds
    • C10N2010/02Groups 1 or 11
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Abstract

Calcium mahogany sulphonate is prepared from crude sodium mahogany sulphonate by blending the crude sodium sulphonate with mineral oil and petroleum thinners, washing the blend with dilute aqueous sodium chloride to remove sodium sulphate and then emulsifying with aqueous calcium chloride. Inorganic salts are removed from the oil phase by water washes and the thinners and the water are removed by heating at reduced pressure. The product is a mineral oil solution of calcium mahogany sulphonate. Calcium dialkyl benzene sulphonate is prepared from a dialkyl benzene obtained by alkylating benzene with polypropylene of molecular weight of about 170, using hydrofluoric acid as alkylating catalyst. The dialkyl benzene is sulphonated with fuming sulphuric acid and the sulphonated material neutralized with aqueous caustic soda. The crude sodium dialkyl benzene sulphonate is converted to a mineral oil solution of the corresponding calcium sulphonate using the procedure employed above for calcium mahogany sulphonate.ALSO:A stable dispersion of lead, magnesium or alkaline earth metal oxides or hydroxides in lubricating oil is prepared by forming a mixture of the lubricating oil, a dihydric alcohol having less than 6 carbon atoms in the molecule, the oxide or hydroxide and a polyvalent metal sulphonate, phosphonate or naphthenate. The dispersion may be employed as the lubricant in an internal combustion engine and any acid formed by oxidation of the lubricating oil during operation of the engine is neutralized by the oxide or hydroxide. Lubricating oils mentioned are mineral oils, other hydrocarbon oils such as those derived from coal and alkylene polymers and other synthetic oils. Synthetic lubricating oils referred to include alkylene oxide polymers and their esters and ethers, esters of dicarboxylic acids, esters of phosphoric acid and esters of phosphonic acids. Suitable dihydric alcohols containing less than 6 carbon atoms in the molecule are ethylene glycol, propylene glycol, butane diol-2, 3, pentane diol-2, 4, 2-methyl butane diol-1, 2, 2-methyl butane diol-2, 4 and 2-methyl butane diol-3, 4. Subsequent to the formation of the dispersion, however, the dihydric alcohol may be removed by distilling. Specified polyvalent metal suphonates are calcium and magnesium white oil benzene sulphonates (prepared from sulphonic acids obtained by alkylating benzene with chlorinated white oil and then sulphonating), calcium and magnesium dipolypropene benzene sulphonates (prepared from sulphonic acids obtained by dialkylating benzene with polypropene so that the alkyl radicles introduced in the benzene molecule have an average of 14 carbon atoms and then sulphonating), calcium and magnesium mahogany sulphonate, calcium and magnesium triacontyl sulphonate, and calcium and magnesium lauryl sulphonate. Specified polyvalent metal naphthenates are the Ca, Ba, Zn, Pb, Sr. Mg, Mn and Cu salts of petroleum naphthenic acids. A dispersion of the oxide or hydroxide in the alcohol may first be prepared and this dipersion then added to a blend of the lubricating oil and the sulphonate, phosphonate or naphthenate. The lubricating oil compositions may contain additional ingredients such as oxidation inhibitors, pour point depressants, corrosion inhibitors, oiliness agents, extreme pressure agents, blooming agents, viscosity index improvers, grease-forming agents and other dispersants. Oxidation inhibitors mentioned are organic esters of phosphous (e.g. calcium or zinc cetyphenyl dithiophosphate), metal salts of thiocarbamic acids (e.g. zinc dibutyl dithiocarbamate), sulphides (e.g. sulphurized diparaffin sulphide, sulphurized olefins and P2S5-pinene reaction products), and amines (e.g. phenyl alpha naphthylamine, 1, 4-diamino 2-dodecyl anthraquinone and p, p1-dioctyl diphenyl amine). In the examples lubricating compositions are described consisting of mineral lubricating oil, calcium oxide, ethylene glycol and calcium naphthenate or calcium mahogany sulphonate, the ethylene glycol is some cases being removed by distilling subsequently to the formation of the dispersion. In a further example, a lubricating composition comprises mineral lubricating oil, sulphurized diparaffin sulphide (the paraffin radicle being derived from a petroleum wax, sulphurized calcium phenate, zinc cetyl phenyl dithiophosphate, calcium mahogany sulphonate and calcium oxide (which has been dispersed in the oil, according to the procedure set out above, with the aid of the calcium mahogany sulphonate). Tests are described in which this lubricating composition of the example is compared with a similar composition from which the calcium oxide has been omitted. Specification 648,328, [Group IV (b)], is referred to.
GB19393/51A 1950-12-30 1951-08-16 Lubricating oil compositions Expired GB718714A (en)

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US203783A US2676925A (en) 1950-12-30 1950-12-30 Method of dispersing metal oxides and hydroxides in lubricating oils

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GB718714A true GB718714A (en) 1954-11-17

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DE (1) DE1002491B (en)
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DE1002491B (en) 1957-02-14
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