GB806915A - Complex metal salts of oxidised petroleum oils - Google Patents

Complex metal salts of oxidised petroleum oils

Info

Publication number
GB806915A
GB806915A GB17114/55A GB1711455A GB806915A GB 806915 A GB806915 A GB 806915A GB 17114/55 A GB17114/55 A GB 17114/55A GB 1711455 A GB1711455 A GB 1711455A GB 806915 A GB806915 A GB 806915A
Authority
GB
United Kingdom
Prior art keywords
oil
per cent
mixture
hydroxide
metal
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
GB17114/55A
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.)
ExxonMobil Oil Corp
Original Assignee
Socony Mobil Oil Co Inc
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 Socony Mobil Oil Co Inc filed Critical Socony Mobil Oil Co Inc
Publication of GB806915A publication Critical patent/GB806915A/en
Expired 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • C07C51/418Preparation of metal complexes containing carboxylic acid moieties
    • 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • 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
    • C10M2225/00Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2225/04Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of macromolecualr compounds not containing phosphorus in the monomers
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • 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
    • C10N2040/25Internal-combustion engines
    • 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
    • C10N2060/00Chemical after-treatment of the constituents of the lubricating composition
    • C10N2060/04Oxidation, e.g. ozonisation
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Lubricants (AREA)

Abstract

Mineral lubricating oils comprise as detergent additives minor amounts of oil solutions of complex metal salts obtained by (1) forming a mixture of a petroleum oil having an average molecular weight of about 300-1000 and about 2-25 per cent, based on the weight of oil, of an hydroxide of a Group II metal; (2) oxidizing the oil in the mixture with a free-oxygen-containing gas at about 250-600 DEG F., the reaction time being sufficient to effect reaction of about 5-85 per cent by weight of the metal hydroxide with the oxidized oil; (3) providing a mixture comprising unchanged petroleum oil solution of oxidized oil-metal hydroxide reaction product formed in step 2, a Group II metal hydroxide to the extent of at least about 2 per cent up to about 40 per cent by weight of the oil used to prepare in step 2 the oil solution used in this step, and water at a temperature below the boiling-point of water; (4) substantially completely dehydrating the resulting mixture; and (5) filtering the dehydrated mixture to separate the oil solution of complex metal salt (see Group IV (b)). The detergent solutions described in the examples are prepared from refined Mid-Continent bright stocks (average M.W. 720 or 880) or an East Texas heavy waxy distillate stock (M.W. 470); in most cases calcium hydroxide is used in both steps 1 and 3, being sometimes the unchanged hydroxide present at the end of the oxidation, but in one case calcium hydroxide is used in step 1 and barium hydroxide in step 3. These solutions, which as exemplified, contain from 1.7 to 7.2 per cent by weight of Group II metal, may be used in amounts of from about 1-10 per cent by weight of the lubricating oil, if desired in conjunction with other additives such as anti-oxidants, pour-point depressants, V.I. improvers, defoamants and rust preventatives. Comparisons are made between the lubricating properties of an SAE20 base oil containing a pinene-P2S5 reaction product as an antioxidant and either one of the detergent oil solutions mentioned above or the corresponding intermediate oil solution obtained at the end of the oxidation step and filtered.ALSO:Oil solutions of complex metal salts of oxidized petroleum oil are prepared by (1) forming a mixture comprising a petroleum oil having an average M.W. of from about 300 to about 1000 and about 2 to about 25 per cent, based on the weight of oil, of an hydroxide of a metal of Group II; (2) contacting the mixture with a free-oxygen containing gas at a temperature of from about 250 DEG to about 600 DEG F., to effect oxidation of the oil, the reaction time being sufficient to effect reaction of from about 5 to about 85 per cent by weight of the metal oxide with the oxidized oil; (3) providing a mixture comprising oxidized oil-metal hydroxide reaction product in unchanged petroleum oil produced in step 2, a hydroxide of a Group II metal to the extent of at least 2 per cent up to about 40 per cent, based on the weight of oil used to prepare the amount of oil solution of reaction product which is used in this step, and water at a temperature below the boiling-point of water; (4) substantially completely dehydrating the mixture formed in step 3; and (5) subjecting the dehydrated mixture to filtration to separate the resulting oil solution of the complex metal salt product, a diluent solvent being used, if desired, to facilitate the filtration. The oxidation may be effected with air or oxygen, preferably at about 350-450 DEG F., and a catalyst may be present. In forming the mixture in step (3), the required metal hydroxide may comprise unchanged metal hydroxide present at the end of the oxidation or may be added after filtration of oxidation product. The water generally amounts to about 2 to 50 per cent by weight of the oxidation product, 2 to 10 per cent being preferred. The dehydration may be effected by heating whilst passing nitrogen through the mixture or by azeotropic distillation, e.g. with benzene. The products are utilizable as detergents in mineral lubricating oils (see Group III) and also as components in coating compositions, paint driers, detergent soaps, dispersants and rust-preventive compositions. In typical examples: (1) a refined Mid-Continent bright stock (M.W. 720) admixed with 7.2 per cent calcium hydroxide is airoxidized at 375 DEG F. and the product is cooled and filtered when about half the metal hydroxide has reacted; 400 gms. of the filtrate are mixed with 135 mols. of 10 per cent aqueous Ca(OH)2 and the mixture is dehydrated at 420 DEG F. and filtered, the filtrate then containing 2.24 per cent Ca; (3) a similar bright stock (M.W. 880) admixed with 11 per cent Ca(OH)2 is air-oxidized in like manner with about 30 per cent of the hydroxide being consumed; the unfiltered reacted mixture is then cooled, water is added and subsequently is stripped off at 400 DEG F., yielding after filtration an oil solution containing 2.43 per cent Ca; a comparative experiment is given showing the lower Ca content obtained when the air-oxidation is effected in the absence of the metal hydroxide, the oxidation product then being diluted with toluene, mixed with water and about 20 per cent Ca(OH)2 and thereafter dehydrated and filtered; (5) the bright stock of (3) in admixture with about 22 per cent Ca(OH)2 is similarly oxidized and the product is filtered, diluted with toluene, admixed with water and barium hydroxide and then dried and filtered yielding an oil solution containing 0.73 per cent Ca and 6.5 per cent Ba. Magnesium, strontium and zinc hydroxides are other specified metal hydroxides. An additional example uses an East Texas heavy, waxy distillate stock of M.W. 470.
GB17114/55A 1954-07-06 1955-06-14 Complex metal salts of oxidised petroleum oils Expired GB806915A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US806915XA 1954-07-06 1954-07-06

Publications (1)

Publication Number Publication Date
GB806915A true GB806915A (en) 1959-01-07

Family

ID=22158999

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17114/55A Expired GB806915A (en) 1954-07-06 1955-06-14 Complex metal salts of oxidised petroleum oils

Country Status (1)

Country Link
GB (1) GB806915A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1286247B (en) * 1959-12-23 1969-01-02 British Petroleum Co Process for the production of surface-active substances

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1286247B (en) * 1959-12-23 1969-01-02 British Petroleum Co Process for the production of surface-active substances

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