US20060019842A1 - Aluminum complex grease - Google Patents

Aluminum complex grease Download PDF

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Publication number
US20060019842A1
US20060019842A1 US11/214,649 US21464905A US2006019842A1 US 20060019842 A1 US20060019842 A1 US 20060019842A1 US 21464905 A US21464905 A US 21464905A US 2006019842 A1 US2006019842 A1 US 2006019842A1
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aluminum
compound
complex grease
aluminum complex
aluminium
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US11/214,649
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Peter Finmans
Christina Diblitz
Frank Allmuller
Detlef Hoell
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Sasol Solvents Germany GmbH
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Sasol Germany GmbH
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Priority to US11/214,649 priority Critical patent/US20060019842A1/en
Assigned to SASOL GERMANY GMBH reassignment SASOL GERMANY GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ALLMULLER, FRANK, DIBLITZ, CHRISTINA, FINMANS, PETER, HOELL, DETLEF
Publication of US20060019842A1 publication Critical patent/US20060019842A1/en
Assigned to SASOL SOLVENTS GERMANY GMBH reassignment SASOL SOLVENTS GERMANY GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SASOL GERMANY GMBH
Abandoned legal-status Critical Current

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    • 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
    • C10M123/00Lubricating compositions characterised by the thickener being a mixture of two or more compounds covered by more than one of the main groups C10M113/00 - C10M121/00, each of these compounds being essential
    • 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
    • C07C51/412Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/06Aluminium compounds
    • C07F5/069Aluminium compounds without C-aluminium linkages
    • 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
    • C10M115/00Lubricating compositions characterised by the thickener being a non-macromolecular organic compound other than a carboxylic acid or salt thereof
    • C10M115/04Lubricating compositions characterised by the thickener being a non-macromolecular organic compound other than a carboxylic acid or salt thereof containing 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
    • C10M117/00Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof
    • C10M117/02Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof having only one carboxyl group bound to an acyclic carbon atom, cycloaliphatic carbon atom or hydrogen
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    • 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
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    • 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
    • C10M2203/102Aliphatic fractions
    • 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
    • C10M2207/006Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions used as thickening agents
    • 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
    • C10M2207/0206Hydroxy compounds used as thickening agents
    • 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
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    • 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/0413Ethers; Acetals; Ortho-esters; Ortho-carbonates used as thickening agent
    • 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
    • C10M2207/09Metal enolates, i.e. keto-enol metal complexes
    • C10M2207/095Metal enolates, i.e. keto-enol metal complexes used as thickening agent
    • 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
    • C10M2207/122Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
    • C10M2207/1225Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic used as thickening agent
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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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
    • 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
    • C10M2207/1265Carboxylix 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 used as thickening agent
    • 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
    • C10M2207/16Naphthenic acids
    • C10M2207/166Naphthenic acids used as thickening agents
    • 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
    • C10M2207/18Tall oil acids
    • C10M2207/186Tall oil acids used as thickening agents
    • 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
    • C10M2207/20Rosin acids
    • C10M2207/206Rosin acids used as thickening agents
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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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
    • C10M2207/24Epoxidised acids; Ester derivatives thereof
    • C10M2207/246Epoxidised acids; Ester derivatives thereof used as thickening agents
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    • 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
    • C10N2010/06Groups 3 or 13

Definitions

  • This invention relates to a thickener component based on an aluminium carboxylate compound and to an aluminium complex grease made therefrom with addition of a base liquid.
  • Aluminium complex greases have been known. They essentially comprise a mineral-oil base liquid and a thickener system containing one or more aluminium carboxylate compounds.
  • the aluminium carboxylate compound is obtained by reacting a fatty acid and/or an aromatic carboxylic acid with an aluminium alcoholate derivative.
  • the industrially used aluminium alcoholates comprise aluminium isopropoxylate and tri-oxy-aluminium-triisopropoxide. In theory, the reaction proceeds as shown hereinbelow:
  • Aluminium complex greases are distinguished by a high dropping point, good conveyance and water resistance, and low separation of oil.
  • the term ‘more effective’ shall mean that the grease exhibits better lubricating properties than conventional aluminium complex greases.
  • the thickener component employed for making said aluminium complex greases be storable and marketable as such, thus enabling the grease manufacturer to produce the thickener-containing grease himself.
  • hydrolysable aluminium compounds refers to aluminium compounds that are capable of forming aluminium-oxygen bonds by the action of protondonating compounds, such as water or organic acids.
  • hydrolysable aluminium compounds are aluminium alcoholate- or aluminium-oxo-alcoholate compounds with the alcoholate group preferably being a C 2 - to C 4 -alcohol, particularly isopropanolate.
  • the carboxylic acids can be branched or unbranched aliphatic monocarboxylic acids of the type R 1 —COOH, wherein R 1 represents a C 10 - to C 40 -radical, preferably a C 14 - to C 24 -radical, or a C 16 - to C 24 -radical.
  • Carboxylic acid derivatives as used herein are defined as compounds which are capable of forming in combination with said aluminium compounds the aluminium-carboxylate bonds that would likewise be obtained when using the corresponding acids. Examples thereof include the anhydrides, acid chlorides, or amides of the aforesaid carboxylic acids.
  • Ester compounds as used herein particularly refer to compounds which may be formed by reaction of the alcohols/alcoholates present in the reaction mixture with the carboxylic acids/carboxylate residues.
  • the thickener component is prepared by reaction, preferably about equimolar reaction, i.e. about 1 mole of monocarboxylic acid per mole of aluminium atoms in the compound, of a hydrolysable aluminium compound with one or more of the abovementioned carboxylic acid(s) or carboxylic acid derivative(s) at a temperature not exceeding 145° C., most preferably 135° C., with a temperature profile most preferably increasing gradually by at least 20° C. during a period of at least 90 minutes being ensured. It is preferred that the hydrolysable aluminium compound be placed in the vessel first.
  • reaction be carried out in a base liquid and the volatile compound released during the reaction, e.g. alcohol, be withdrawn from the equilibrium.
  • volatile compound released during the reaction e.g. alcohol
  • thickener as used herein is defined as a compound or mixture of compounds prepared from the thickener component, which thickener can be produced by reacting the thickener component with aromatic or cyclic monocarboxylic acids of the type R 2 —COOH, wherein R 2 represents a C 6 - to C 16 -radical, or with the derivatives thereof.
  • aromatic or cyclic monocarboxylic acids of the type R 2 —COOH, wherein R 2 represents a C 6 - to C 16 -radical, or with the derivatives thereof.
  • Said (aromatic or cyclic) carboxylic acid derivatives are defined as described hereinabove.
  • aromatic monocarboxylic acid is defined as a carboxylic acid which has at least one benzene ring or condensed benzene ring and, in addition, may comprise aliphatic hydrocarbon radicals as well.
  • compounds such as C 6 H 5 —CH 2 —CH 2 —. COOH or CH 3 —CH 2 —C 6 H 4 —COOH are explicitly included herein.
  • the thickener as a constituent of the aluminium complex grease is produced by compounding the thickener component, optionally taken up in additional base liquid, with the aromatic or cyclic monocarboxylic acid.
  • the production process of the invention ‘yields a raw material (thickener component) with a low ester content for making the real thickener that keeps its low ester content even upon storage.
  • the aluminium complex greases of the invention also comprise a base liquid which is a hydrocarbon compound and/or a synthetic oil added to the overall composition in quantities of from 30 to 98 weight percent, preferably 60 to 95 weight percent.
  • the hydrocarbon compound can be a paraffin-base or naphthenic mineral oil, a polyalphaolefin, or a white oil.
  • Further synthetic oils which are suitable as base liquid include fatty acid esters based on mono- or multifunctional fatty acids having a chain length of from 8 to 24 carbon atoms and mono- or polyhydric alcohols. Additional constituents of the aluminium complex greases of the invention may be typical additives. Table 1 presents examples of suitable additives.
  • the thickener components of the invention are useful as raw materials for producing thickeners included in aluminium complex greases exhibiting improved lubricating properties. They are preferably employed in high-temperature applications for which high dropping points are especially desirable, in central lubricators, and/or for lubricating machinery used for example for producing or processing foodstuffs.
  • the thickener components as well contain 20 to 80 weight percent, most preferably 30 to 70 weight percent of the base liquid described hereinabove.
  • Example 4 presents a high ester concentration, whereas the ester concentration in Example 5 (comparative example) is too high.
  • the measurements were made on a thickener component having an aluminium content of 4.1 weight percent.
  • the solvent in the aluminium-containing thickener component is identical with the base oil.
  • the starting material is aluminium isopropanolate.
  • the aliphatic monocarboxylic acid employed herein is a technical-grade stearic acid mixture.

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  • 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)
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Abstract

This invention relates to a thickener component based on an aluminium carboxylate compound and to an aluminium complex grease made therefrom with addition of a base liquid.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application is a divisional of U.S. patent application Ser. No. 10/221,336 filed on Feb. 03, 2003, for Thickener Component and Aluminum Complex Grease, the disclosure of which is incorporated herein by reference.
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • This invention relates to a thickener component based on an aluminium carboxylate compound and to an aluminium complex grease made therefrom with addition of a base liquid.
  • 2. Description of the Prior Art
  • Aluminium complex greases have been known. They essentially comprise a mineral-oil base liquid and a thickener system containing one or more aluminium carboxylate compounds. The aluminium carboxylate compound is obtained by reacting a fatty acid and/or an aromatic carboxylic acid with an aluminium alcoholate derivative. The industrially used aluminium alcoholates comprise aluminium isopropoxylate and tri-oxy-aluminium-triisopropoxide. In theory, the reaction proceeds as shown hereinbelow:
    Figure US20060019842A1-20060126-C00001
  • When using aluminium isopropoxylate, partial hydrolysis is performed with water before, during, or after reaction of the acids with aluminium alcoholate to produce the usually required free -OH group on the aluminium. Aluminium complex greases are distinguished by a high dropping point, good conveyance and water resistance, and low separation of oil.
  • SUMMARY OF THE INVENTION
  • It is an object of this invention to provide more effective aluminium complex greases, in particular more suitable thickener components for manufacturing thickeners for aluminium complex greases. The term ‘more effective’ shall mean that the grease exhibits better lubricating properties than conventional aluminium complex greases. Furthermore, it is desired that the thickener component employed for making said aluminium complex greases be storable and marketable as such, thus enabling the grease manufacturer to produce the thickener-containing grease himself.
  • According to this invention, the problem has been resolved by providing a thickener component comprising
      • (A) from 99.99 to 94 weight percent, preferably 99.9 to 97 weight percent of an aluminium compound which can be prepared by reacting a hydrolysable aluminium compound with one or more aliphatic monocarboxylic acid(s) or aliphatic derivatives thereof, optionally in the presence of water and/or a C1- to C40-alcohol, thereby forming one or more aluminium compound(s) having at least one aluminium carboxylate bond per aluminium atom and, in addition, one or more aluminium-, hydroxy-, aluminium alcoholate-, and/or aluminium-oxygen-aluminium bond(s) and
      • (B) from 0.01 to 6 weight percent, preferably 0.1 to 3 weight percent of an ester compound having from 6 to 60 carbon atoms,
        each referring to the total of components (A) and (B).
    DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • The term ‘hydrolysable aluminium compounds’ as used herein refers to aluminium compounds that are capable of forming aluminium-oxygen bonds by the action of protondonating compounds, such as water or organic acids. Preferably, such hydrolysable aluminium compounds are aluminium alcoholate- or aluminium-oxo-alcoholate compounds with the alcoholate group preferably being a C2- to C4-alcohol, particularly isopropanolate. The carboxylic acids can be branched or unbranched aliphatic monocarboxylic acids of the type R1—COOH, wherein R1 represents a C10- to C40-radical, preferably a C14- to C24-radical, or a C16- to C24-radical.
  • Carboxylic acid derivatives as used herein are defined as compounds which are capable of forming in combination with said aluminium compounds the aluminium-carboxylate bonds that would likewise be obtained when using the corresponding acids. Examples thereof include the anhydrides, acid chlorides, or amides of the aforesaid carboxylic acids.
  • Ester compounds as used herein particularly refer to compounds which may be formed by reaction of the alcohols/alcoholates present in the reaction mixture with the carboxylic acids/carboxylate residues.
  • The thickener component is prepared by reaction, preferably about equimolar reaction, i.e. about 1 mole of monocarboxylic acid per mole of aluminium atoms in the compound, of a hydrolysable aluminium compound with one or more of the abovementioned carboxylic acid(s) or carboxylic acid derivative(s) at a temperature not exceeding 145° C., most preferably 135° C., with a temperature profile most preferably increasing gradually by at least 20° C. during a period of at least 90 minutes being ensured. It is preferred that the hydrolysable aluminium compound be placed in the vessel first.
  • Moreover, it is preferred that the reaction be carried out in a base liquid and the volatile compound released during the reaction, e.g. alcohol, be withdrawn from the equilibrium.
  • The term ‘thickener’ as used herein is defined as a compound or mixture of compounds prepared from the thickener component, which thickener can be produced by reacting the thickener component with aromatic or cyclic monocarboxylic acids of the type R2—COOH, wherein R2 represents a C6- to C16-radical, or with the derivatives thereof. Said (aromatic or cyclic) carboxylic acid derivatives are defined as described hereinabove.
  • The resultant aluminium compound preferably has more than 40 mole % of aliphatic monocarboxylic acid radicals, referring to the amount of carboxylate groups (100 mole %=all the carboxylate groups). The remainder is comprised of aromatic or cyclic monocarboxylic acid radicals. As used herein, the term ‘aromatic monocarboxylic acid’ is defined as a carboxylic acid which has at least one benzene ring or condensed benzene ring and, in addition, may comprise aliphatic hydrocarbon radicals as well. Hence, compounds such as C6H5—CH2—CH2—. COOH or CH3—CH2—C6H4—COOH are explicitly included herein.
  • The thickener as a constituent of the aluminium complex grease is produced by compounding the thickener component, optionally taken up in additional base liquid, with the aromatic or cyclic monocarboxylic acid.
  • The production process of the invention ‘yields a raw material (thickener component) with a low ester content for making the real thickener that keeps its low ester content even upon storage.
  • Besides the thickeners of the invention the aluminium complex greases of the invention also comprise a base liquid which is a hydrocarbon compound and/or a synthetic oil added to the overall composition in quantities of from 30 to 98 weight percent, preferably 60 to 95 weight percent.
  • The hydrocarbon compound can be a paraffin-base or naphthenic mineral oil, a polyalphaolefin, or a white oil. Further synthetic oils which are suitable as base liquid include fatty acid esters based on mono- or multifunctional fatty acids having a chain length of from 8 to 24 carbon atoms and mono- or polyhydric alcohols. Additional constituents of the aluminium complex greases of the invention may be typical additives. Table 1 presents examples of suitable additives.
  • The thickener components of the invention are useful as raw materials for producing thickeners included in aluminium complex greases exhibiting improved lubricating properties. They are preferably employed in high-temperature applications for which high dropping points are especially desirable, in central lubricators, and/or for lubricating machinery used for example for producing or processing foodstuffs.
  • The prior art thickeners based on aluminium carboxylate compounds or the aluminium complex greases made therefrom have significantly higher ester concentrations. Surprisingly, compositions with lower ester concentrations, preferably less than 6 % in the thickener component, and improved lubricating properties have now become accessible by the process.
  • It is preferred that the thickener components as well contain 20 to 80 weight percent, most preferably 30 to 70 weight percent of the base liquid described hereinabove.
  • Examples of Tests
  • Table 2 shows the rheometric values (Physica UDS 200, oscillating measurement, deformation=0.2%, frequency=0.1 Hz, temperature 20° C., plate/plate distance=1 mm) of aluminium complex greases of the invention. Example 4 presents a high ester concentration, whereas the ester concentration in Example 5 (comparative example) is too high. The measurements were made on a thickener component having an aluminium content of 4.1 weight percent. The solvent in the aluminium-containing thickener component is identical with the base oil. The starting material is aluminium isopropanolate. The aliphatic monocarboxylic acid employed herein is a technical-grade stearic acid mixture.
  • Exemplary Synthesis
  • Into a 5-litre agitated vessel equipped with a nitrogen supply line, a 30-cm column (metalized, packed with Raschig rings), and a reflux condenser there are placed 1.466 moles (299.5 g) of DOROX® D 10 (aluminium triisopropylate, liquid) and 500.0 g of Sera® 100 mineral oil (approx. 50 wt. % paraffin-base oil). The educts are heated to 97° C. (bottom temperature) while stirring. The stearic acid is heated to 75-80° C. to keep the product liquid upon feeding. 1.466 moles (393.5 g) of the liquid stearic acid (acid number=209 mg of KOH/g) and the mixture of water (1.372 moles=24.7 g) and 2-propanol (123.6 g) are charged steadily and simultaneously through separate submerged pipes during a period of 2.5 hours. The released 2-propanol is removed overhead (head temperature max. 85° C.). The bottom temperature is gradually increased to 127° C. during this period. Once the bottom temperature reaches 127° C., the pressure is reduced to 200 hPa during 20 minutes and the remainder of the low-boiling 2-propanol is drawn off. During the reaction a distillate comprised of 3.623 moles (217.7 g) of 2-propanol is removed from the reaction and the mixture (123.6 g). The product, oxo-aluminium-stearate, is obtained after purification and filtration. The total residence time of the product at 127° C. is 30 minutes (until end of vacuum phase). Filtration is performed at approx. 120° C. using a 60-μm sieve.
  • The material parameters of the thickener component have been compiled in Table 3.
    TABLE 1
    Concentration
    Range, wt. %
    Extreme-pressure   2-10 dibenzyldisulfide with
    additives chlorinated paraffins;
    sulphurized fatty oils
    or terpenes
    Additives for enhancing 0.1-5 diisopropyl- or dilauryl
    film resistance hydrogen phosphite
    Rust-inhibiting additives 0.5-5 sodium petroleum sulfo-
    nates or barium dinonyl
    naphthalene sulfonate
    Copper deactivators 0.05-1  2-mercaptobenzthiazol
    Viscosity index improvers 0.1-1 polymethacrylates
    Desludgers 0.001 silicone oils
    Additives for producing 0.5-2 polymers
    ropiness
    Antiwear additives 0.1-2 tricresylic phosphate,
    zinc dialkyl dithio-
    phosphate
    Additives for producing 0.1-2 oil- or other vegetable
    water resistance fatty acids
    Deodorants  0.05-0.5 perfumes
    Anticorrosion additives 0.5-3 nonylphenoxy vinegar,
    ethylenediamine
    sulfonate, lead
    dinonylnaphthyl sul-
    fonate, barium sulfo-
    nates, lead- and zinc
    naphthenates
    Oxidation inhibitors diphenylamine, phenyl-
    α-naphthylamine, di-
    octyldiphenylamine,
    phenothiazine, poly-
    meric trimethyldi-
    hydroquinoline, 2,6-
    di-tert-butyl-4-
    methylphenol, lead
    diamyldithiocarbamate,
    dilaurylthiodipro-
    pionate-1/citric acid,
    ascorbic acid
  • TABLE 2
    Base Liquid Ester Concen- Base Liquid Thickener
    Base Liquid Concentra- tration in Concentration Component Benzoic Acid
    Viscosity tion in Thickener in Thickener Concentration Concentration Modulus of Modulus of
    at 40° C. Grease Component Component in Grease in Grease Elasticity Viscosity
    No. Base Liquid mm2/s wt. % wt. % wt. % wt. % wt. % Pa Pa
    1 Paraffin- 100 91.3 1.4 60 7.3 1.4 860 330
    based
    mineral oil
    2 Paraffin- 100 87.1 1.4 60 10.9 2.0 5,720 1,030
    based
    mineral oil
    3 Paraffin- 100 82.8 1.4 60 14.5 2.7 35,100 5,400
    based
    mineral oil
    4 Paraffin- 100 87.1 3.9 60 10.9 2.0 1,100 270
    based
    mineral oil
    5 Paraffin- 100 87.1 8.7 60 10.9 2.0 800 170
    based
    mineral oil
    6 Naphthene- 100 87.1 1.2 50 10.9 2.0 5,820 1,000
    based
    mineral oil
    7 Naphthene- 40 87.1 1.2 50 10.9 2.0 2,680 450
    based
    mineral oil
    8 Polyalpha- 30 91.3 2.4 60 7.3 1.4 290 60
    olefin
    9 Polyalpha- 30 87.1 2.4 60 10.9 2.0 2,100 290
    olefin
    10 Polyalpha- 30 82.8 2.4 60 14.5 2.7 13,300 1,100
    olefin
  • TABLE 3
    Method
    Al content 4.1% M 635
    Turbidity 20 FNU DIN 38404 T2
    Viscosity(25° C.) 1,500 mPa · s DIN 53015
    Viscosity (100° C.) 100 mPa · s Rotation (200s−1)
    Pour point 16° C. DIN ISO 3016
    2-Propanol concentration 3.5%
    Density (20° C.) 0.94 g/cm3 DIN 51757
    Density (40° C.) 0.93 g/cm3 DIN 51757
    Density (50° C.) 0.93 g/cm3 DIN 51757
    Flash point 190° C. DIN 51758
    Colour number 10 DIN 6162

Claims (12)

1-8. (canceled)
9. An aluminum complex grease comprising
a compound or compound mixture obtainable by reacting an ester thickener component with at least one aromatic and/or cyclic monocarboxylic acid, of the type R1—COOH, wherein R1 is a C6 to C16 organic moiety, and/or their derivatives and
a base liquid selected from the group consisting of hydrocarbon compounds, synthetic oils and mixtures thereof, said base liquid being present in the grease in an amount of from 30 to 98 weight percent
wherein the thickener component comprises
(A) from 99.99 to 94 weight percent of an aluminum compound obtainable by an approximately equimolar reaction of a hydrolysable aluminum compound with at least one aliphatic monocarboxylic acid or derivatives thereof, in the presence of water and a C1- to C40-alcohol to form one or more aluminum compound(s) having on average one aluminum carboxylate bond per aluminum atom and, in addition, one or more aluminum-hydroxy, aluminum-alcoholate, or aluminum-oxygen-aluminum bond(s) and
(B) from 0.01 to 6 weight percent of an ester compound having from 6 to 60 carbon atoms,
the weight percentage referring to the total of components (A) and (B).
10. An aluminum complex grease of claim 9, characterized in that the hydrolysable aluminum compound is an aluminum-alcoholate or aluminum-oxo-alcoholate compound.
11. An aluminum complex grease according to claim 9, characterized in that the base liquid has a viscosity of from 20 to 200 mm2/s at 40° C. measured in accordance with DIN 51562.
12. An aluminum complex grease according to claim 9, characterized in that the base liquid is a mineral oil with a boiling point of greater than 250° C.
13. An aluminum complex grease according to claim 9, wherein the base liquid is present in an amount of from 60 to 95 weight percent.
14. An aluminum complex grease according to claim 9, characterized in that said aliphatic monocarboxylic acid is selected from the group consisting of branched or unbranched aliphatic monocarboxylic acids of the type R2—COOH, wherein R2 is a C10- to C40-radical, or a derivative thereof.
15. An aluminum complex grease according to claim 14, wherein said R2 is a C14- to C24-radical.
16. An aluminum complex grease according to claim 9, characterized in that a temperature of 145° C. is not exceeded during the preparation of the aluminum thickener compound by reacting said hydrolysable aluminum compound with said carboxylic acid or said carboxylic acid derivative.
17. An aluminum complex grease of claim 16, wherein the temperature does not exceeded 135° C.
18. An aluminum complex grease according to any one of claims 16 and 17, characterized in that an increasing temperature profile presenting a temperature difference of at least 20° C. is maintained at a time interval of at least 90 min during the reaction.
19. An aluminum complex grease according to claim 9, wherein the aluminium compound/compound mixture of the aluminum complex grease obtained has more than 40 mol % of aliphatic monocarboxylic acid radicals, referring to the amount of carboxylate groups, the reminder being aromatic and/or cyclic monocarboxylic acid radicals.
US11/214,649 2000-03-10 2005-08-30 Aluminum complex grease Abandoned US20060019842A1 (en)

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PCT/DE2001/000829 WO2001066675A2 (en) 2000-03-10 2001-03-06 Thickener component and lubricating grease containing an aluminium complex
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US7288506B2 (en) * 2002-11-27 2007-10-30 Baker Hughes Incorporated Aluminum carboxylate drag reducers for hydrocarbon emulsions
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Citations (8)

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US2768138A (en) * 1952-10-18 1956-10-23 California Research Corp Complex basic aluminum soap greases
US3345291A (en) * 1963-12-17 1967-10-03 Chevron Res Production of complex basic aluminum soap greases
US3591505A (en) * 1968-06-18 1971-07-06 Sun Oil Co Aluminum complex soap greases
US3620975A (en) * 1968-07-03 1971-11-16 Sun Oil Co Mixed complex aluminum soap-clay grease composition
US3791972A (en) * 1972-01-13 1974-02-12 Southwest Petro Chem Inc Lubricating grease
US5075473A (en) * 1989-05-03 1991-12-24 Komaromi Koolajipari V. Process for the preparation of aluminum oxide carboxylate polymers containing at most two percent by weight of ester
US5358664A (en) * 1992-10-15 1994-10-25 Caschem, Inc. Gelled oil compositions
US5387351A (en) * 1993-05-18 1995-02-07 Kumar; Anoop Lubricating grease composition and process for preparing same

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EP0029589B1 (en) * 1979-11-23 1984-07-04 Chattem, Inc. Process for making grease compositions
GB2269169A (en) * 1992-07-24 1994-02-02 Rhone Poulenc Chemicals Aluminium complexes useful for cross-linking coating compositions

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Publication number Priority date Publication date Assignee Title
US2768138A (en) * 1952-10-18 1956-10-23 California Research Corp Complex basic aluminum soap greases
US3345291A (en) * 1963-12-17 1967-10-03 Chevron Res Production of complex basic aluminum soap greases
US3591505A (en) * 1968-06-18 1971-07-06 Sun Oil Co Aluminum complex soap greases
US3620975A (en) * 1968-07-03 1971-11-16 Sun Oil Co Mixed complex aluminum soap-clay grease composition
US3791972A (en) * 1972-01-13 1974-02-12 Southwest Petro Chem Inc Lubricating grease
US5075473A (en) * 1989-05-03 1991-12-24 Komaromi Koolajipari V. Process for the preparation of aluminum oxide carboxylate polymers containing at most two percent by weight of ester
US5358664A (en) * 1992-10-15 1994-10-25 Caschem, Inc. Gelled oil compositions
US5387351A (en) * 1993-05-18 1995-02-07 Kumar; Anoop Lubricating grease composition and process for preparing same

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WO2001066675A3 (en) 2002-06-27
US20040097381A1 (en) 2004-05-20

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