Nothing Special   »   [go: up one dir, main page]

US3857789A - Slushing oil or rust inhibiting compositions - Google Patents

Slushing oil or rust inhibiting compositions Download PDF

Info

Publication number
US3857789A
US3857789A US00084540A US8454070A US3857789A US 3857789 A US3857789 A US 3857789A US 00084540 A US00084540 A US 00084540A US 8454070 A US8454070 A US 8454070A US 3857789 A US3857789 A US 3857789A
Authority
US
United States
Prior art keywords
percent
composition
weight
acid
sulfonate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US00084540A
Inventor
A Nassry
F Krupin
J Beiswanger
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.)
Rhone Poulenc Surfactants and Specialties LP
Bayer CropScience Inc USA
Original Assignee
GAF Corp
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 GAF Corp filed Critical GAF Corp
Priority to US00084540A priority Critical patent/US3857789A/en
Application granted granted Critical
Publication of US3857789A publication Critical patent/US3857789A/en
Assigned to CHASE MANHATTAN BANK, THE NATIONAL ASSOCIATION reassignment CHASE MANHATTAN BANK, THE NATIONAL ASSOCIATION SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DORSET INC. A CORP OF DELAWARE
Assigned to GAF CHEMICALS CORPORATION reassignment GAF CHEMICALS CORPORATION CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). EFFECTIVE ON 04/11/1989 Assignors: DORSET INC.
Assigned to RHONE-POULENC SPECIALTY CHEMICALS, L.P. reassignment RHONE-POULENC SPECIALTY CHEMICALS, L.P. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: GAF CHEMICALS CORPORATION
Assigned to DORSET INC., A DE CORP. reassignment DORSET INC., A DE CORP. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). EFFECTIVE APRIL 10, 1989 Assignors: GAF CORPORATION, A DE CORP.
Assigned to DORSET INC., reassignment DORSET INC., RELEASED BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: CHASE MANHATTAN BANK, THE,
Assigned to RHONE - POULENC SPECIALITY CHEMICALS reassignment RHONE - POULENC SPECIALITY CHEMICALS A CORRECTIVE ASSIGNMENT TO CORRECT THE SINGLE SERIAL NUMBER 07194,259 IDENTIFIED IN PREVIOUSLY RECORDED ASSIGMENT ON REEL 5315/FRAME 589. THIS CORRECTIVE ASSIGMENT SHOWS THAT THERE SHOULD HAVE BEEN A SCHEDULE ATTACHED. Assignors: GAF CHEMICALS CORPORATION
Assigned to RHONE-POULENC SURFACTANTS AND SPECIALTIES, L.P. reassignment RHONE-POULENC SURFACTANTS AND SPECIALTIES, L.P. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: RHONE-POULENC SPECIALTY CHEMICALS, L.P.
Assigned to RHONE-POULENC SURFACTANTS AND SPECIALTIES INC. reassignment RHONE-POULENC SURFACTANTS AND SPECIALTIES INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). EFFECTIVE ON 05/03/1990 Assignors: RHONE-POULENC SPECIALTY CHEMICALS INC.
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • 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
    • C10M2203/02Well-defined aliphatic 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/022Well-defined aliphatic compounds saturated
    • 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
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/024Well-defined aliphatic compounds unsaturated
    • 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
    • C10M2203/04Well-defined cycloaliphatic 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
    • 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
    • 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/104Aromatic 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/106Naphthenic 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/108Residual fractions, e.g. bright stocks
    • 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
    • C10M2207/021Hydroxy 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
    • 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/044Cyclic ethers having four or more ring atoms, e.g. furans, dioxolanes
    • 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/046Hydroxy ethers
    • 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
    • C10M2207/128Carboxylix 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 containing hydroxy groups; Ethers 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
    • C10M2207/129Carboxylix 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
    • 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
    • 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
    • C10M2215/225Heterocyclic 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
    • C10M2215/30Heterocyclic 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
    • 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
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives

Definitions

  • the present invention is directed toward a novel rust inhibiting composition and, more particularly, to a combination of rust inhibitors in a suitable lubricating medium, wherein the slushing oil so provided has enhanced rust inhibiting characteristics due to the presence of a metal salt of a mahogany or naphthalene sulfonic acid and a higher fatty acid of 1560 carbon atoms.
  • rust inhibiting compositions which, when applied as a coating, will have the effect of preventing the formation of rust over extended periods of time.
  • the coating of a rust inhibiting paint has been applicable where the iron object is stationary and, accordingly, not subject to wear, etc., as would be the case if the iron object was part of a moving mechanism. Therefore, in such environment, wherein the object is stationary, a thick rust inhibiting coating of paint is generally capable of preventing rust over extended periods of time.
  • a rust inhibiting composition comprising in combination a metal salt of a phosphate ester or a mixture of phosphate esters, plus an aliphatic carboxylic acid of -60 carbon atoms, e.g., a dimer acid.
  • a further combination of a metal salt of a mahogany or naphthalene sulfonic acid and a higher aliphatic carboxylic acid, e.g., dimer acid, in a lubricating oil medium in the presence of a cosolvent provides further enhanced rust inhibition characteristics and such composition is eminently suitable for the inhibiting of rust of iron objects subject to wear and abrasion.
  • It is yet a further object of the present invention to provide such a slushing oil comprising a metal salt of a mahogany or naphthalene sulfonic acid, a higher aliphatic carboxylic acid, e.g., dimer acid, a cosolvent therefor, and a paraffinic or naphthenic lubricating oil.
  • Such a combination of components providing enhanced rust inhibiting characteristics is generally employed in combination with (c) a cosolvent for the sulfonate and aliphatic carboxylic acid, and (d) a lubricating oil, e.g., paraffinic or napthenic lubricating oil.
  • compositions of the present invention in the form of slushing oils or fluids are particularly adapted for the rust prevention of iron objects subjected to movement generally causing wear and abrasion. It is within this environment that the compositions of the present invention provide for objects and advantages not obtainable with conventional rust inhibiting paints.
  • a primary component of the slushing oil or fluid of the present invention comprises a metal salt of a mahogany sulfonic acid or naphthalene sulfonic acid.
  • metal salts of mahogany or naphthalene sulfonic acids are materials which are well any sulfonic acid or mahogany sulfonate is meant to embrace any and all of the aforedescribed oil-soluble derivatives well known in the art.
  • naphthalene sulfonic acids or naphthalene sulfonates are well known materials which are commercially available.
  • naphthalene sulfonates are alkyl substituted naphthalene sulfonic acid derivatives wherein the alkyl groups have from 8 to about 30 carbon atoms.
  • suitable naphthalene sulfonates in accordance with the present invention include such materials dioctyl naphthalene sulfonate dinonyl naphthalene sulfonate decyl naphthalene sulfonate dodecyl naphthalene sulfonate tridecyl naphthalene sulfonate tetradecyl naphthalene sulfonate hexadecyl naphthalene sulfonate octadecyl naphthalene sulfonate eicosyl naphthalene sulfonate, etc. 7
  • the mahogany or naphthalene sulfonates are employed in the novel rust inhibiting composition of the present invention as their metallic salts.
  • the suitable metals for producing the mahogany or naphthalene sulfonate salts are metals of Groups IIA, IIIA and IVA of the Periodic Table. Specifically preferred metals for the production of the metal salts include barium, calcium, strontium, lead and aluminum.
  • a suitable mahogany sulfonate comprises Bryton Ba-3ON or Bryton Ca-3ON, respectively being the barium salt and calcium salt of mahogany sulfonate marketed by Bryton Chemical Company, a division of Continental Oil Co.
  • Bryton Chemical Company a division of Continental Oil Co.
  • the above terms are trademarks of the Bryton Chemical Co.
  • a suitable naphthalene sulfonate in accordance with the present invention comprises a material known as NA-SUL-BSN, which is the barium salt of dinonyl naphthalene sulfonate NA-SUL- BSN is a registered trademark for the above identified product which is marketed by the R. T. Vanderbilt Co. Inc.
  • the second component of the novel synergistic rust inhibiting composition of the present invention is a higher fatty acid containing from -60 carbon atoms.
  • higher fatty acids include linoleic acid, linolenic acid, ricinoleic acid, palmitic acid, stearic acid, or mixtures thereof.
  • the preferred fatty acid component of the novel synergistic rust inhibiting composition of the present invention comprises the dimer acids which conventionally contain from -60 carbon atoms.
  • a particularly preferred component is dimer acid, adimer of linoleic acid having 36 carbon atoms.
  • Suitable commercial dimer acids are sold by Emery Industries under the names of Empol 1010 dimer acid containing 97 percent of the dimer of linoleic acid, 3 percent of the trimer of linoleic aicd, and substantially no mono-basic acids.
  • the commercial dimer acids for example, contain varying amounts of the trimer of linoleic acid and mono-basic acid.
  • a dimer acid sold as Empol 1022 contains 75 percent of the dimer, 22 percent trimer, and 3 percent mono-basic acids
  • Empol 1016 contains 87 percent dimer, 13 percent trimer, with only a trace of mono-basic acids. All such commercial formulations can be advantageously employed in accordance with the present invention,
  • dimer acid produced by the dimerization of linoleic acid is not precisely known, it is hypothesized that the dimer acid has a structural formula as follows:
  • Typical specifications of a commercial product containing approximately 85 percent of the dimer of linoleic acid, 12 percent of the trim'er of linoleic acid, and about 3 percent of the monomeric acid are as follows:
  • the enhanced rust inhibition associated with the combination of components in accordance with the present invention is achieved when the metal salts of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid are present in amounts from about 10 to about 90 percent and 90 to about 10 percent by weight, respectively.
  • the rust inhibiting composition of the present invention containing only the metal salts of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid contains about 20 to percent by weight of such sulfonate and 80 to 20 percent by weight of the higher aliphatic carboxylic acid, e.g., dimer acid.
  • COSOLVENT As indicatedabove, the combination of components,- i.e., metal salt of a mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid, is generally employed in the form' of a slushing fluid or oil wherein such components are dissolved in a mineral oil, e.g., paraffinic or naphthenic oil, in the presence of a cosolvent.
  • a mineral oil e.g., paraffinic or naphthenic oil
  • the cosolvent for the metal salt of mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid can comprise an aromatic or heterocyclic solvent, or a vari-
  • a class of well known glycol ethers is particularly adapted for use in accordance with the present invention.
  • such a preferred class of cosolvents includes the monoand dialkyl ethers of ethylene, diethylene and triethylene glycols and similar propylene glycols wherein the alkyl group contains from I to 6 carbon atoms.
  • Such preferred cosolvents employed in accordance with the present invention are exemplified by ethylene glycol monobutyl ether.
  • any material which acts as a solvent for both the metal salt of the mahogany or naphthalene sulfonic acid and dimer acid can be advantageously utilized in accordance with the present invention and the selection of a proper solvent is governed primarily by such solubility considerations. Accordingly, while the above list is exemplary, it is not in any way meant to embrace all of the conventional solvent materials which can be advantageously utilized in accordance with the rust inhibiting composition of the present invention.
  • the novel rust inhibiting composition of the present invention is generally employed in the form of a slushing oil or fluid wherein a mineral oil comprises the vehicle therefor.
  • the mineral oil vehicle may be a paraffinic or naphthenic oil ranging in viscosity from 50 to 300 SUS at 100F.
  • Naphthenic oils are preferred in accordance with the present invention since the metal salt of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid are more readily soluble in naphthenic type oils.
  • the vehicle in accordance with the present invention can comprise other well known petroleum based oils and lubricants.
  • the vehicle for the slushing oil or fluid having enhanced rust inhibiting characteristics can comprise a conventional ester type lubricant, silicon oil, etc.
  • the vehicle for the slushing oil fluid be a paraffinic or naphthenic oil, preferably a naphthenic oil, ranging in viscosity from 50 to 300 SUS at 100F.
  • the amount of the various components are generally as follows:
  • the final composition is generally prepared merely by adding and mixing the metal salt of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid to the mineral oil vehicle with subsequent addition of the cosolvent, preferably the glycol ether. After a homogeneous solution is prepared by mixing, a final amount of mineral oil is added to the system to bring the same up to the final concentration and to provide the homogeneous mixture having enhanced rust inhibiting characteristics.
  • the composition ofthe present invention provides for enhanced or synergistic rust inhibition.
  • the use of the combination of the metal salt of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid, i.e., dimer acid provides for a rust inhibition which is greater than would be expected from the rust inhibiting characteristics of the individual components alone.
  • the composition of the present invention acts both as a rust inhibitor and a lubricant, the same is superior to conventional paint rust inhibitors and can be utilized in those environments wherein an iron object is not stationary and wherein due to movement, the same is normally subjected to wear and abrasion. Accordingly, this constitutes a distinct advantage of the novel compositions of the present invention over conventional rust inhibiting compositions.
  • EXAMPLE 1 Some 19.98 g. of a 30 percent solution of the barium salt of mahogany sulfonate (Bryton Ba-3ON) in a mineral oil SUS solvent refined naphthenic pale oil) were placed in a 16 oz. widemouth, screw-cap bottle.
  • barium salt of mahogany sulfonate Bryton Ba-3ON
  • SUS solvent refined naphthenic pale oil SUS solvent refined naphthenic pale oil
  • dimer acid (Empol 1022) were added. The mixture was blended until homogeneous. Then 9.0 g. of ethylene glycol monobutyl ether were added and the mixture was blended until homogeneous.
  • Table 1 (Rust protection shown by individual components in 100 SUS solvent refined naphthenic pale oil) Additive and Days Protection A homogeneous mixture consisting of 2 percent calcium salt of mahogany sulfonate, Bryton Ca-3ON p 2 percent dimer acid, Empol 1022 3 percent ethylene glycol monobutyl ether 93 percent mineral oil was prepared and tested for rust inhibition in the same manner as described for Example 1. Coated panels remained without rust for 4 days in the Q.C.T. cabinet and for 52 days in the humidity cabinet. Comparing this performance with that of the individual components in Table 1 again shows the superior performance of the combination of ingredients with regard to rust inhibition. 1
  • EXAMPLE 3 Some 12 g. of a 50 percent solution of the barium salt of dinonyl naphthalene sulfonate in a mineral oil were placed in a 16 02., wide-mouth, screw-cap bottle.
  • dimer acid (Empol 1022)
  • the mixture was blended until homogeneous.
  • 9 g. of ethylene glycol monobutyl ether were added.
  • the foregong examples clearly illustrate that the combination of a metal salt of mahogany or naphthalene sulfonic acid and a higher aliphatic carboxylic acid, e.g., dimer acid, provides for enhanced or synergistic results with regard to rust inhibition.
  • a metal salt of mahogany or naphthalene sulfonic acid and a higher aliphatic carboxylic acid, e.g., dimer acid provides for enhanced or synergistic results with regard to rust inhibition.
  • the foregoing examples clearly illustrate that since a mineral oil vehicle is employed, the rust inhibiting composition in the form a slushing oil or fluid possesses both rust inhibiting and lubricating properties. Accordingly, this makes the compositions of the present invention eminently suited for use in those environments wherein the iron object normally subject to rusting is also subjected to wear and abrasion.
  • a rust-inhibiting slushing oil composition compris- A. 0.5 10 percent by weight of a metal salt of amahogany sulfonate or C alkyl substituted naphthalene sulfonate, said metal being selected from groups IlA, "IA and IVA of the Periodic Table;
  • composition of claim 1 wherein said metal is selected from Ba, Ca, Sr, Pb and Al.
  • component (A) is a metal salt of a mahogany sulfonate.
  • component (A) is a metal salt of a C alkyl naphthalene sulfonate.
  • composition ofclaim 4 wherein said C alkyl naphthalene sulfonate is dinonyl naphthalene sulfonate.
  • composition of claim 1 wherein said higher aliphatic carboxylic acid is a dimer acid.
  • composition of claim 6 wherein said dimer acid is a dimer of linoleic acid.
  • composition of claim 1 wherein said cosolvent is a monoor dialkyl ether of ethylene glycol wherein the alkyl group contains from l-6 carbon atoms.
  • composition of claim 8 wherein said cosolvent is ethylene glycol monobutyl ether.
  • composition of claim 1 wherein said mineral oil is selected from paraffinic and naphthenic oils having a viscosity of 50 to 300 SUS at 100F.
  • composition of claim 1 wherein said components (A), (.B), (C) and (D) are present in the follow ing amounts:
  • a rust-inhibiting additive composition comprising:
  • composition of claim 12 wherein said metal is selected from Ba, Ca, Sr, Pb and Al.
  • component (A) is a metal salt of a mahogany sulfonate.
  • component (A) is a metal salt of a C840 alkyl naphthalene sulfonate.
  • composition of claim 12 wherein said higher aliphatic carboxylic acid is a dimer acid.
  • composition of claim 17 wherein said dimer acid is a dimer of linoleic acid.
  • a rust inhibiting slushing oil composition comprising 2 percent by weight of the barium salt of mahogany sulfonate, 2 percent by weight of a dimer of linoleic acid, 3 percent of ethylene glycol monobutyl ether, and 93 percent by weight of a mineral oil.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Abstract

Slushing oil: A. METAL SULFONATE; B. ALIPHATIC CARBOXYLIC ACID AND POLYMERS THEREOF; C. COSOLVENT SELECTED FROM AROMATIC HYDROCARBONS, METHYL PYRROLIDONE, TETRAHYDROFURAN, AND MONO AND DIALKYL ETHERS OF ALKYLENE GLYCOLS AND MIXTURES THEREOF; D. MINERAL LUBRICATING OIL.

Description

United States Patent [1 1 Krupin et al.
[4 1 Dec. 31, 1974 1 SLUSI-IING OIL OR RUST INHIBITING COMPOSITIONS [75] Inventors: Fred Krupin, New York, N.Y.; John P. G. Beiswanger, Audubon; Assadullah Nassry, Bethlehem, both of Pa.
[73] Assignee: GAF Corporation, New York, NY.
[22] Filed: Oct. 27, 1970 [21] Appl. No.: 84,540
[52] US. Cl 252/33.4, 252/51.5 A, 252/52 A, 252/52 R, 252/56 R [51] Int. Cl. Cl0m 1/40, ClOm 1/32 [58] Field of Search..... 252/33, 51.5 'A, 56 R, 52 R, 252/33.4, 52 A, 389
[56] References Cited UNITED STATES PATENTS 2,481,372 9/1949 Fuchs et a1. 242/33.4 2,624,708 1/1953 Langer et al 252/33.4 2,631,979 3/1953 McDermott 252/33.4
2,632,694 3/1953 Watkins 252/33.4
2,632,695 3/1953 Landis et a1. 252/334 2,671,758 3/1954 Vinograd et a1. 252/33.4
Benbury et a1. 252/33.4 Waugh 252/33.4 Beiswanger et a1 252/33.4
McMillen 252/33.4
FOREIGN PATENTS OR APPLICATIONS Canada.-. 252/33.4
Primary Examiner-Daniel E. Wyman Assistant Examiner-I. Vaughn Attorney, Agent, or FirmWalter C. Kehm; Samson B.
Leavitt Slushing oil: I
a. metal sulfonate;
ABSTRACT mixtures thereof;
(1. mineral lubricating oil.
19 Claims, No Drawings SLUSHING OIL OR RUST INHIBITINO COMPOSITIONS The present invention is directed toward a novel rust inhibiting composition and, more particularly, to a combination of rust inhibitors in a suitable lubricating medium, wherein the slushing oil so provided has enhanced rust inhibiting characteristics due to the presence of a metal salt of a mahogany or naphthalene sulfonic acid and a higher fatty acid of 1560 carbon atoms.
Because of the tendency of iron objects to rust when exposed to weather, many attempts have been made to provide rust inhibiting compositions which, when applied as a coating, will have the effect of preventing the formation of rust over extended periods of time. Generally, the coating of a rust inhibiting paint has been applicable where the iron object is stationary and, accordingly, not subject to wear, etc., as would be the case if the iron object was part of a moving mechanism. Therefore, in such environment, wherein the object is stationary, a thick rust inhibiting coating of paint is generally capable of preventing rust over extended periods of time.
It should be obvious, however, that such thick coatings of paint are not applicable wherein movement of the iron object causes wear and abrasion. In such cases, it is necessary to employ some sort of coating which will not lose its rust inhibiting effectiveness upon frictional contact. Therefore, a coating of some sort which acts both as a lubricant and as a rust inhibitor is highly desirable. While this is true, only a very limited number of compositions having the aforedescribed characteristics has been developed prior to the present invention.
One such composition which is extremely effective as a rust inhibitor and which can be effectively utilized in those environments wherein the iron object to be protected is subjected to wear and abrasion is disclosed in copending application, Ser. No. 20,844 filed Mar. 18, 1970, in the names'of John P. G. Beiswanger and Assadullah Nassry and now abandoned. Such application discloses a rust inhibiting composition comprising in combination a metal salt of a phosphate ester or a mixture of phosphate esters, plus an aliphatic carboxylic acid of -60 carbon atoms, e.g., a dimer acid. In accordance with the present invention, however, it has been found that a further combination of a metal salt of a mahogany or naphthalene sulfonic acid and a higher aliphatic carboxylic acid, e.g., dimer acid, in a lubricating oil medium in the presence of a cosolvent provides further enhanced rust inhibition characteristics and such composition is eminently suitable for the inhibiting of rust of iron objects subject to wear and abrasion.
Accordingly, it is a principal object of the present invention to provide a rust inhibiting composition which is unexpectedly superior to previous compositions and which can be advantageously utilized in those environments wherein movement of an iron object tends to cause wear and abrasion.
It is a further object of the present invention to pro vide such a rust inhibiting composition in the form of a slushing fluid or oil wherein the same contains a metal salt of a mahogany or naphthalene sulfonic acid and a higher aliphatic carboxylic acid of 15-60 carbon atoms.
It is yet a further object of the present invention to provide such a slushing oil comprising a metal salt of a mahogany or naphthalene sulfonic acid, a higher aliphatic carboxylic acid, e.g., dimer acid, a cosolvent therefor, and a paraffinic or naphthenic lubricating oil.
Still further objects and advantages of the novel rust inhibiting compositions of the present invention will become more apparent from the following more detailed description thereof.
The foregoing objects and advantages of the present invention are achieved by the utilization ofa combination of components comprising (a) metal salts of mahogany or naphthalene sulfonic acids, and (b) a higher aliphatic carboxylic acid of l5-60 carbon atoms, e.g., dimer acids.
Such a combination of components providing enhanced rust inhibiting characteristics is generally employed in combination with (c) a cosolvent for the sulfonate and aliphatic carboxylic acid, and (d) a lubricating oil, e.g., paraffinic or napthenic lubricating oil.
As indicated above, such a combination of components is effective for preventing the corrosion due to rusting of materials containing iron. In addition, due to the fact that the composition possesses both lubricating and rust inhibiting characteristics, the compositions of the present invention in the form of slushing oils or fluids are particularly adapted for the rust prevention of iron objects subjected to movement generally causing wear and abrasion. It is within this environment that the compositions of the present invention provide for objects and advantages not obtainable with conventional rust inhibiting paints.
METAL SALT OF MAHOGANY OR NAPHTHALENE SULFONIC ACID As indicated above, a primary component of the slushing oil or fluid of the present invention comprises a metal salt of a mahogany sulfonic acid or naphthalene sulfonic acid. Such metal salts of mahogany or naphthalene sulfonic acids are materials which are well any sulfonic acid or mahogany sulfonate is meant to embrace any and all of the aforedescribed oil-soluble derivatives well known in the art.
Similarly, the metal salts of naphthalene sulfonic acids or naphthalene sulfonates are well known materials which are commercially available. Conventionally, such naphthalene sulfonates are alkyl substituted naphthalene sulfonic acid derivatives wherein the alkyl groups have from 8 to about 30 carbon atoms. Thus, for example, suitable naphthalene sulfonates in accordance with the present invention include such materials dioctyl naphthalene sulfonate dinonyl naphthalene sulfonate decyl naphthalene sulfonate dodecyl naphthalene sulfonate tridecyl naphthalene sulfonate tetradecyl naphthalene sulfonate hexadecyl naphthalene sulfonate octadecyl naphthalene sulfonate eicosyl naphthalene sulfonate, etc. 7
As noted previously, the mahogany or naphthalene sulfonates are employed in the novel rust inhibiting composition of the present invention as their metallic salts. In accordance with the present invention, the suitable metals for producing the mahogany or naphthalene sulfonate salts are metals of Groups IIA, IIIA and IVA of the Periodic Table. Specifically preferred metals for the production of the metal salts include barium, calcium, strontium, lead and aluminum.
As indicated above, such metal salts of mahogany and naphthalene sulfonic acids employed in accordance with the present invention are well known and are commercially available. Thus, for example, a suitable mahogany sulfonate comprises Bryton Ba-3ON or Bryton Ca-3ON, respectively being the barium salt and calcium salt of mahogany sulfonate marketed by Bryton Chemical Company, a division of Continental Oil Co. The above terms are trademarks of the Bryton Chemical Co. In addition, a suitable naphthalene sulfonate in accordance with the present invention comprises a material known as NA-SUL-BSN, which is the barium salt of dinonyl naphthalene sulfonate NA-SUL- BSN is a registered trademark for the above identified product which is marketed by the R. T. Vanderbilt Co. Inc.
HIGH FATTY ACID The second component of the novel synergistic rust inhibiting composition of the present invention is a higher fatty acid containing from -60 carbon atoms. Thus, for example, such higher fatty acids include linoleic acid, linolenic acid, ricinoleic acid, palmitic acid, stearic acid, or mixtures thereof. The preferred fatty acid component of the novel synergistic rust inhibiting composition of the present invention comprises the dimer acids which conventionally contain from -60 carbon atoms. A particularly preferred component is dimer acid, adimer of linoleic acid having 36 carbon atoms.
Suitable commercial dimer acids are sold by Emery Industries under the names of Empol 1010 dimer acid containing 97 percent of the dimer of linoleic acid, 3 percent of the trimer of linoleic aicd, and substantially no mono-basic acids. The commercial dimer acids, for example, contain varying amounts of the trimer of linoleic acid and mono-basic acid. Thus, for example, a dimer acid sold as Empol 1022 contains 75 percent of the dimer, 22 percent trimer, and 3 percent mono-basic acids, while Empol 1016 contains 87 percent dimer, 13 percent trimer, with only a trace of mono-basic acids. All such commercial formulations can be advantageously employed in accordance with the present invention,
While the exact structure of the dimer acid produced by the dimerization of linoleic acid is not precisely known, it is hypothesized that the dimer acid has a structural formula as follows:
Typical specifications of a commercial product containing approximately 85 percent of the dimer of linoleic acid, 12 percent of the trim'er of linoleic acid, and about 3 percent of the monomeric acid are as follows:
Viscosity at 100C., centistokes The preparation of such-dimer acid is well known, its preparation being described in the Journal of American Society Oil Chemists, 24, 65 (March, 1947). Again, all such commercial preparations of the dimer acid, as well as the individual components thereof, including all higher fatty acids containing from about 15 to about 60 carbon atoms, can be advantageously employed as a component of the novel synergistic rust inhibiting composition of the present invention.
.In accordance with the present invention, the enhanced rust inhibition associated with the combination of components in accordance with the present invention is achieved when the metal salts of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid are present in amounts from about 10 to about 90 percent and 90 to about 10 percent by weight, respectively. Preferably the rust inhibiting composition of the present invention containing only the metal salts of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid contains about 20 to percent by weight of such sulfonate and 80 to 20 percent by weight of the higher aliphatic carboxylic acid, e.g., dimer acid. Of course, the above ranges are only exemplary and slightly higher or lower amounts of the 1 individual components can be employed in accordance with the present invention, it only being necessary that both the metal salts of the mahogany or naphthalene sulfonic acid and higher fatty acid be present in order to achieve the enhanced rust inhibiting action of the compositon of the present invention.
COSOLVENT As indicatedabove, the combination of components,- i.e., metal salt of a mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid, is generally employed in the form' of a slushing fluid or oil wherein such components are dissolved in a mineral oil, e.g., paraffinic or naphthenic oil, in the presence of a cosolvent. In accordance with the-present invention, the cosolvent for the metal salt of mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid can comprise an aromatic or heterocyclic solvent, or a vari- In addition to the above aromatic and heterocyclic solvents which can be advantageously utilized in accordance with the present invention, a class of well known glycol ethers is particularly adapted for use in accordance with the present invention. Thus, such a preferred class of cosolvents includes the monoand dialkyl ethers of ethylene, diethylene and triethylene glycols and similar propylene glycols wherein the alkyl group contains from I to 6 carbon atoms. Such preferred cosolvents employed in accordance with the present invention are exemplified by ethylene glycol monobutyl ether.
While the above solvents are all suitable in accordance with the present invention, it is pointed out that the above enumerated materials are only exemplary of the cosolvents which can be advantageously utilized. In this regard, any material which acts as a solvent for both the metal salt of the mahogany or naphthalene sulfonic acid and dimer acid can be advantageously utilized in accordance with the present invention and the selection of a proper solvent is governed primarily by such solubility considerations. Accordingly, while the above list is exemplary, it is not in any way meant to embrace all of the conventional solvent materials which can be advantageously utilized in accordance with the rust inhibiting composition of the present invention.
MINERAL OIL As indicated previously, the novel rust inhibiting composition of the present invention is generally employed in the form of a slushing oil or fluid wherein a mineral oil comprises the vehicle therefor. In accordance with the present invention, the mineral oil vehicle may be a paraffinic or naphthenic oil ranging in viscosity from 50 to 300 SUS at 100F. Naphthenic oils are preferred in accordance with the present invention since the metal salt of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid are more readily soluble in naphthenic type oils.
In addition to the mineral oils of a paraffinic or naphthenic nature, the vehicle in accordance with the present invention can comprise other well known petroleum based oils and lubricants. Thus, for example, the vehicle for the slushing oil or fluid having enhanced rust inhibiting characteristics can comprise a conventional ester type lubricant, silicon oil, etc. Again, however, it is preferred in accordance with the present invention that the vehicle for the slushing oil fluid be a paraffinic or naphthenic oil, preferably a naphthenic oil, ranging in viscosity from 50 to 300 SUS at 100F.
In accordance with the present invention, when the combination of components is employed in a slushing fluid or oil with a cosolvent and a mineral oil vehicle, the amount of the various components are generally as follows:
Component Amount by Weight Metal salt of mahogany sulfonate or In accordance with the present invention, the above In preparing the slushing oil or fluid in accordance with the present invention, no special precautions or proceduresneed be taken in producing the final composition. In this regard, the final composition is generally prepared merely by adding and mixing the metal salt of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid to the mineral oil vehicle with subsequent addition of the cosolvent, preferably the glycol ether. After a homogeneous solution is prepared by mixing, a final amount of mineral oil is added to the system to bring the same up to the final concentration and to provide the homogeneous mixture having enhanced rust inhibiting characteristics.
As indicated previously, the composition ofthe present invention provides for enhanced or synergistic rust inhibition. Thus, as will be shown hereinafter, the use of the combination of the metal salt of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid, i.e., dimer acid, provides for a rust inhibition which is greater than would be expected from the rust inhibiting characteristics of the individual components alone. Moreover, since the composition of the present invention acts both as a rust inhibitor and a lubricant, the same is superior to conventional paint rust inhibitors and can be utilized in those environments wherein an iron object is not stationary and wherein due to movement, the same is normally subjected to wear and abrasion. Accordingly, this constitutes a distinct advantage of the novel compositions of the present invention over conventional rust inhibiting compositions.
The novel compositions of the present invention will now be illustrated by reference to the following specific examples. In such examples which are presented for purposes of illustration only, all parts are by weight unless otherwise specified.
EXAMPLE 1 Some 19.98 g. of a 30 percent solution of the barium salt of mahogany sulfonate (Bryton Ba-3ON) in a mineral oil SUS solvent refined naphthenic pale oil) were placed in a 16 oz. widemouth, screw-cap bottle.
Then 6.0 g. of dimer acid (Empol 1022) were added. The mixture was blended until homogeneous. Then 9.0 g. of ethylene glycol monobutyl ether were added and the mixture was blended until homogeneous.
Thereafter 265.0 g. of mineral oil (100 SUS solvent refined naphthenic pale oil) were added. The final mixture was stirred at room temperature giving a homogeneous mixture containing:
2 parts of barium salt of mahogany sulfonate 2 parts of dimer acid 3 parts of ethylene glycol monobutyl. ether 93 parts of mineral oil Rust inhibition was evaluated as follows:
Mild steel panels which conformed to specifications in ASTM D-l748 and which had been cleaned according to the referenced test method, were dipped in the oil solution. They were allowed to drain for 16-24 hours and were then placed in the Q.C.T. cabinet and humidity cabinet to determine the extent of rust protection obtained. Panels remained without rust for 4-5 days in the Q.C.T. cabinet and for more than 100 days in the humidity cabinet without rust.
The individual components, when tested in a like manner, gave significantly less protection as shown in Table 1. It should be noted that in these tests of the individual components, the metal salts were used at even higher concentration than used in the subject composition. It is, accordingly, apparent that the combination of ingredients gives much better performance than the single components.
Table 1 (Rust protection shown by individual components in 100 SUS solvent refined naphthenic pale oil) Additive and Days Protection A homogeneous mixture consisting of 2 percent calcium salt of mahogany sulfonate, Bryton Ca-3ON p 2 percent dimer acid, Empol 1022 3 percent ethylene glycol monobutyl ether 93 percent mineral oil was prepared and tested for rust inhibition in the same manner as described for Example 1. Coated panels remained without rust for 4 days in the Q.C.T. cabinet and for 52 days in the humidity cabinet. Comparing this performance with that of the individual components in Table 1 again shows the superior performance of the combination of ingredients with regard to rust inhibition. 1
EXAMPLE 3 Some 12 g. ofa 50 percent solution of the barium salt of dinonyl naphthalene sulfonate in a mineral oil were placed in a 16 02., wide-mouth, screw-cap bottle.
Then 6 g. of dimer acid (Empol 1022) were added. The mixture was blended until homogeneous. Then 9 g. of ethylene glycol monobutyl ether were added.
Thereafter, 283 g. of 100 SUS solvent refined naphthenic pale oil were added to the mixture. This final mixture was stirred at room temperature giving a homogeneous mixture which contained 2 percent barium salt of dinonyl naphthalene sulfonate 2 percent dimer acid 3 percent ethylene glycol monobutyl ether 92 percent mineral oil Coated panels remained without rust for 3-4 days in the Q.C.T. cabinet and for 108-1 18 days in the humidity cabinet. Comparing this performance with that of the individual components in Table 1 again demonstrates the superior performance of the combination of ingredients.
EXAMPLE 4 Example 1 is repeated except in lieu of the barium salt of mahogany sulfonate as employed in such example, the following metal salts of mahogany or naphthalene sulfonic acids were utilized in substantially the same amounts by weight:
Sr salt of mahogany sulfonate Pb salt of mahogany sulfonate Al salt of mahogany sulfonate Ca salt of dioctyl naphthalene sulfonate Ba salt of dodecyl naphthalene sulfonate Ba salt of tetradecyl naphthalene sulfonate Ca salt of octadecyl naphthalene sulfonate Sr salt of dionyl napt halene' sulfonate Al salt of dinonyl naphthalene sulfonate When slushing oil compositions containing the foregoing metal salts of mahogany or naphthalene sulfonic acids were tested as in Example 1, substantially the same rust inhibiting characteristics were observed.
EXAMPLE 5 EXAMPLE 6 Example 1 is again repeated except that in lieu of the dimer acid, the following higher aliphatic carboxylic.
acids were employed in amounts substantially equivalent by weight:
linoleic acid ricinoleic acid stearic acid dimer of linoleic acid trimer of linoleic acid Again when such slushing oils are tested as in Example l, substantially equivalent'rust inhibition is observed.
EXAMPLE 7 Example 2 was repeated except that the following homogeneous mixtures were prepared:
4 percent calcium salt of mahogany sulfonate, Bryton Ca-3ON 3 percent dimer acid, Empol 1022 2 percent ethylene glycol monobutyl ether 89 percent SUS solvent refined naphthenic pale oil 6 percent calcium salt of mahogany sulfonate, Bryton Ca-3ON 5 percent dimer acid, Empol 1022 9 20 ethylene glycol monobutyl ether 69 percent 100 SUS solvent refined naphthenic pale oil 3 percent calcium salt of mahogany sulfonate, Bryton Ca-3ON 5 percent dimer acid, Empol 1022 5 percent ethylene glycol monobutyl ether 87 percent 100 SUS solvent refined naphthenic pale oil 8 percent calcium salt of mahogany sulfonate, Bryton Ca-3ON 8 percent dimer acid, Empol 1022 2 percent ethylene glycol monobutyl ether 82 percent 100 SUS solvent refined naphthenic pale oil 1 percent calcium salt of mahogany sulfonate, Bryton Ca-3ON 1 percent dimer acid, Empol 1022 5 percent ethylene glycol monobutyl ether 93 percent 100 SUS solvent refined naphthenic pale oil 10 percent salt of mahogany sulfonate, Bryton Ca- 10 percent dimer acid, Empol 1022 30 percent ethylene glycol monobutyl ether 50 percent 100 SUS solvent refined naphthenic pale oil 0.7 percent calcium salt of mahogany sulfonate, Bryton Ca-3ON 1.0 percent dimer acid, Empol 1022 1.0 percent ethylene glycol monobutyl ether 97.3 percent 100 SUS solvent refined naphthenic pale oil The above compositions were tested for rust inhibition as described in Example 1. In all cases, the results were comparable to those set forth in Example 2.
The foregong examples clearly illustrate that the combination of a metal salt of mahogany or naphthalene sulfonic acid and a higher aliphatic carboxylic acid, e.g., dimer acid, provides for enhanced or synergistic results with regard to rust inhibition. In addition, the foregoing examples clearly illustrate that since a mineral oil vehicle is employed, the rust inhibiting composition in the form a slushing oil or fluid possesses both rust inhibiting and lubricating properties. Accordingly, this makes the compositions of the present invention eminently suited for use in those environments wherein the iron object normally subject to rusting is also subjected to wear and abrasion.
While certain preferred embodiments of the present invention have been illustrated by way of specific examples. it should be understood that the present invention is in no way to' be deemed limited thereto, but should be construed as broadly as all and any of the equivalents thereof.
We claim:
1. A rust-inhibiting slushing oil composition compris- A. 0.5 10 percent by weight ofa metal salt of amahogany sulfonate or C alkyl substituted naphthalene sulfonate, said metal being selected from groups IlA, "IA and IVA of the Periodic Table;
B. 0.5 10 percent by weight of a higher aliphatic fatty carboxylic acid of about to 60 carbon atoms and polymers thereof,
C. 0.5 30 percent by weight of a cosolvent for (A) and (B) said solvent being selected from the group consisting of aromatic hydrocarbons, methyl pyrrolidone, tetrahydrofuran, and mono and dialkyl ethers of alkylene glycols and mixtures thereof; and
D. 50 98.5 percent by weight of a mineral oil.
2. The composition of claim 1 wherein said metal is selected from Ba, Ca, Sr, Pb and Al.
3. The composition of claim 2 wherein component (A) is a metal salt of a mahogany sulfonate.
4. The composition of claim 2 wherein component (A) is a metal salt of a C alkyl naphthalene sulfonate.
5. The composition ofclaim 4 wherein said C alkyl naphthalene sulfonate is dinonyl naphthalene sulfonate.
6. The composition of claim 1 wherein said higher aliphatic carboxylic acid is a dimer acid.
7. The composition of claim 6 wherein said dimer acid is a dimer of linoleic acid.
8. The composition of claim 1 wherein said cosolvent is a monoor dialkyl ether of ethylene glycol wherein the alkyl group contains from l-6 carbon atoms.
9. The composition of claim 8 wherein said cosolvent is ethylene glycol monobutyl ether.
10. The composition of claim 1 wherein said mineral oil is selected from paraffinic and naphthenic oils having a viscosity of 50 to 300 SUS at 100F.
11. The composition of claim 1 wherein said components (A), (.B), (C) and (D) are present in the follow ing amounts:
A. 2 6 percent by weight B. 2 6 percent by weight C. 3 18 percent by weight D. 93 percent by weight.
12. A rust-inhibiting additive composition comprising:
A. a metal salt of a mahogany sulfonate or C alkyl substituted naphthalene sulfonate, said metal being selected from groups IIA, "IA and IVA of the periodic table; and B. a higher aliphatic fatty carboxylic acid of about 15 to about 60 carbon atoms and polymers thereof said components (A) and (B) being present in amounts of from about 10 to about percent by weight and about 90 to about 10 percent by weight respectively.
13. The composition of claim 12 wherein said metal is selected from Ba, Ca, Sr, Pb and Al.
14. The composition of claim 13 wherein component (A) is a metal salt of a mahogany sulfonate.
15. The composition of claim 13 wherein component (A) is a metal salt of a C840 alkyl naphthalene sulfonate.
16. The composition of claim 15 wherein said C alkyl naphthalene sulfonate is dinonyl naphthalene sulfonate.
17. The composition of claim 12 wherein said higher aliphatic carboxylic acid is a dimer acid.
18. The composition of claim 17 wherein said dimer acid is a dimer of linoleic acid.
19. A rust inhibiting slushing oil composition comprising 2 percent by weight of the barium salt of mahogany sulfonate, 2 percent by weight of a dimer of linoleic acid, 3 percent of ethylene glycol monobutyl ether, and 93 percent by weight of a mineral oil.

Claims (19)

1. A RUST-INHIBITING SLUSHING OIL CMPOSITION COMPRISING: A. 0.5 - 10 PERCENT BY WEIGHT OF A METAL SALT OF A MAHOGANY SULFONATE ORR C8-30 ALKYL SUBSTITUTED NAPHTHALENE SULFONATE SAID METAL BEING SELECTED FROM GROUPS IIA, IIIA, AND IVA OF THE PERIODIC TABLE: B. 0.5 - 10 PERCENT BY WEIGHT OF A HIGHER APLIPHATIC FATTY CARBOXYLIC ACID OF ABOUT 15 TO 60 CARBON ATOMS AND POLYMERS THEREOF; C. 0.5 - 30 PERCENT BY WEIGHT OF A COSOLVENT FOR (A) AND (B) SAID SOLVENT BEING SELECTED FROM THE GROUP CONSISTING OF AROMATIC HYDROCARBONS, METHYL PYRROLIDONE, TETRAHYDROFURAN, AND MONO AND DIALKYL ETHER OF ALKYLENE GLYCOLS AND MIXTURES THEREOF; AND D. 50 - 98.5 PERCENT BY WEIGHT OF A MINERAL OIL.
2. The composition of claim 1 wherein said metal is selected from Ba, Ca, Sr, Pb and Al.
3. The composition of claim 2 wherein component (A) is a metal salt of a mahogany sulfonate.
4. The composition of claim 2 wherein component (A) is a metal salt of a C8-30 alkyl naphthalene sulfonate.
5. The composition of claim 4 wherein said C8-30 alkyl naphthalene sulfonate is dinonyl naphthalene sulfonate.
6. The composition of claim 1 wherein said higher aliphatic carboxylic acid is a dimer acid.
7. The composition of claim 6 wherein said dimer acid is a dimer of linoleic acid.
8. The composition of claim 1 wherein said cosolvent is a mono-or dialkyl ether of ethylene glycol wherein the alkyl group contains from 1-6 carbon atoms.
9. The composition of claim 8 wherein said cosolvent is ethylene glycol monobutyl ether.
10. The composition of claim 1 wherein said mineral oil is selected from paraffinic and naphthenic oils having a viscosity of 50 to 300 SUS at 100*F.
11. The composition of claim 1 wherein said components (A), (B), (C) and (D) are present in the following amounts: A. 2 - 6 percent by weight B. 2 - 6 percent by weight C. 3 - 18 percent by weight D. 70 - 93 percent by weight.
12. A rust-inhibiting additive composition comprising: A. a metal salt of a mahogany sulfonate or C8-30 alkyl substituted naphthalene sulfonate, said metal being selected from groups IIA, IIIA and IVA of the periodic table; and B. a higher aliphatic fatty carboxylic acid of about 15 to about 60 carbon atoms and polymers thereof said components (A) and (B) being present in amounts of from about 10 to about 90 percent by weight and about 90 to about 10 percent by weight respectively.
13. The composition of claim 12 wherein said metal is selected from Ba, Ca, Sr, Pb and Al.
14. The composition of claim 13 wherein component (A) is a metal salt of a mahogany sulfonate.
15. The composition of claim 13 wherein component (A) is a metal salt of a C8-30 alkyl naphthalene sulfonate.
16. The compOsition of claim 15 wherein said C8-30 alkyl naphthalene sulfonate is dinonyl naphthalene sulfonate.
17. The composition of claim 12 wherein said higher aliphatic carboxylic acid is a dimer acid.
18. The composition of claim 17 wherein said dimer acid is a dimer of linoleic acid.
19. A rust inhibiting slushing oil composition comprising 2 percent by weight of the barium salt of mahogany sulfonate, 2 percent by weight of a dimer of linoleic acid, 3 percent of ethylene glycol monobutyl ether, and 93 percent by weight of a mineral oil.
US00084540A 1970-10-27 1970-10-27 Slushing oil or rust inhibiting compositions Expired - Lifetime US3857789A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US00084540A US3857789A (en) 1970-10-27 1970-10-27 Slushing oil or rust inhibiting compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US00084540A US3857789A (en) 1970-10-27 1970-10-27 Slushing oil or rust inhibiting compositions

Publications (1)

Publication Number Publication Date
US3857789A true US3857789A (en) 1974-12-31

Family

ID=22185607

Family Applications (1)

Application Number Title Priority Date Filing Date
US00084540A Expired - Lifetime US3857789A (en) 1970-10-27 1970-10-27 Slushing oil or rust inhibiting compositions

Country Status (1)

Country Link
US (1) US3857789A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4224173A (en) * 1978-06-12 1980-09-23 Michael Ebert Lubricant oil containing polytetrafluoroethylene and fluorochemical surfactant
US4264653A (en) * 1979-09-24 1981-04-28 Pennwalt Corporation Coating of steel
US4396515A (en) * 1980-03-28 1983-08-02 Cincinnati Vulcan Company Coating oil compositions
US4834894A (en) * 1980-12-29 1989-05-30 Tribophysics Corporation PTFE oil additive
US5001013A (en) * 1989-08-15 1991-03-19 Cincinnati-Vulcan Company Coating oil having improved electrocoat compatibility
US5741763A (en) * 1995-12-22 1998-04-21 Exxon Research And Engineering Company Lubricant oil composition
US20140303055A1 (en) * 2006-03-29 2014-10-09 Kyodo Yushi Co., Ltd. Lubricant Composition

Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2481372A (en) * 1946-09-27 1949-09-06 Shell Dev Rust protective lubricants
US2624708A (en) * 1950-06-23 1953-01-06 Union Carbide & Carbon Corp Inhibited polyoxyalkylene glycol fluids
US2631979A (en) * 1950-08-30 1953-03-17 Standard Oil Dev Co Rust inhibiting composition
US2632695A (en) * 1951-09-20 1953-03-24 Socony Vacuum Oil Co Inc Rust inhibitor for light petroleum products
US2632694A (en) * 1950-11-14 1953-03-24 Sinclair Refining Co Petroleum distillates containing ammonium mahogany sulfonates and oil soluble carboxylic acids to prevent corrosion
US2671758A (en) * 1949-09-27 1954-03-09 Shell Dev Colloidal compositions and derivatives thereof
US2739126A (en) * 1954-01-25 1956-03-20 Bray Chemical Company Corrosion preventive oils
US2773036A (en) * 1951-12-27 1956-12-04 Tidewater Oil Company Extreme pressure soluble oil compositions
US2883277A (en) * 1956-10-12 1959-04-21 Gen Aniline & Film Corp Synergistic corrosion inhibiting composition for gasoline
US2904415A (en) * 1956-05-23 1959-09-15 Nat Aluminate Corp Non-corrosive petroleum distillates
CA615549A (en) * 1961-02-28 B. Sheldahl David Water dispersible slushing composition
US3004917A (en) * 1959-05-14 1961-10-17 Exxon Research Engineering Co Oil compositions containing rust inhibitors
US3242078A (en) * 1960-12-16 1966-03-22 Exxon Research Engineering Co Suspending colloidal calcium carbonate in hydrocarbon oils
US3242079A (en) * 1962-04-06 1966-03-22 Lubrizol Corp Basic metal-containing thickened oil compositions

Patent Citations (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA615549A (en) * 1961-02-28 B. Sheldahl David Water dispersible slushing composition
US2481372A (en) * 1946-09-27 1949-09-06 Shell Dev Rust protective lubricants
US2671758A (en) * 1949-09-27 1954-03-09 Shell Dev Colloidal compositions and derivatives thereof
US2624708A (en) * 1950-06-23 1953-01-06 Union Carbide & Carbon Corp Inhibited polyoxyalkylene glycol fluids
US2631979A (en) * 1950-08-30 1953-03-17 Standard Oil Dev Co Rust inhibiting composition
US2632694A (en) * 1950-11-14 1953-03-24 Sinclair Refining Co Petroleum distillates containing ammonium mahogany sulfonates and oil soluble carboxylic acids to prevent corrosion
US2632695A (en) * 1951-09-20 1953-03-24 Socony Vacuum Oil Co Inc Rust inhibitor for light petroleum products
US2773036A (en) * 1951-12-27 1956-12-04 Tidewater Oil Company Extreme pressure soluble oil compositions
US2739126A (en) * 1954-01-25 1956-03-20 Bray Chemical Company Corrosion preventive oils
US2904415A (en) * 1956-05-23 1959-09-15 Nat Aluminate Corp Non-corrosive petroleum distillates
US2883277A (en) * 1956-10-12 1959-04-21 Gen Aniline & Film Corp Synergistic corrosion inhibiting composition for gasoline
US3004917A (en) * 1959-05-14 1961-10-17 Exxon Research Engineering Co Oil compositions containing rust inhibitors
US3242078A (en) * 1960-12-16 1966-03-22 Exxon Research Engineering Co Suspending colloidal calcium carbonate in hydrocarbon oils
US3242079A (en) * 1962-04-06 1966-03-22 Lubrizol Corp Basic metal-containing thickened oil compositions

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4224173A (en) * 1978-06-12 1980-09-23 Michael Ebert Lubricant oil containing polytetrafluoroethylene and fluorochemical surfactant
US4264653A (en) * 1979-09-24 1981-04-28 Pennwalt Corporation Coating of steel
US4396515A (en) * 1980-03-28 1983-08-02 Cincinnati Vulcan Company Coating oil compositions
US4834894A (en) * 1980-12-29 1989-05-30 Tribophysics Corporation PTFE oil additive
US5001013A (en) * 1989-08-15 1991-03-19 Cincinnati-Vulcan Company Coating oil having improved electrocoat compatibility
US5741763A (en) * 1995-12-22 1998-04-21 Exxon Research And Engineering Company Lubricant oil composition
US20140303055A1 (en) * 2006-03-29 2014-10-09 Kyodo Yushi Co., Ltd. Lubricant Composition
US9376644B2 (en) * 2006-03-29 2016-06-28 Kyodo Yushi Co., Ltd. Lubricant composition

Similar Documents

Publication Publication Date Title
US4053426A (en) Lubricant compositions
CA1283399C (en) Grease composition
US2956020A (en) Anti-corrosion compositions
US4193882A (en) Corrosion inhibited lubricant composition
US2631979A (en) Rust inhibiting composition
US2481372A (en) Rust protective lubricants
JPS58171488A (en) Lubricating oil composition
US2775560A (en) Corrosion inhibitting lubricating compositions
US2412634A (en) Lubricant
US2564422A (en) Corrosion preventive composition
US3857789A (en) Slushing oil or rust inhibiting compositions
US3004916A (en) Lubricating oil
FI85159C (en) Useful reaction product of triaxol and amine phosphate in lubricant
US2382699A (en) Slushing oil compositions
US3169116A (en) Corrosion inhibiting compsoitions
EP0295108B1 (en) Corrosion inhibiting composition
US2602049A (en) Antioxidants for mineral oil lubricants and compositions containing the same
US3121057A (en) Succinamic metal salts in turbine oil
US2908648A (en) Corrosion-inhibited compositions containing n-(alkylarylsulfonyl) amino acids and salts thereof
US4052322A (en) Corrosion-inhibited grease compositions
US2533300A (en) Morpholine mahogany sulfonate as a rust inhibitor for petroleum oils
US3214377A (en) Phenylamides of organoamine polyacetic acids as anti-oxidants in greases
US2359738A (en) Rust-preventive compositions
US3203896A (en) Lubricating composition
US3359202A (en) Lubricating compositions

Legal Events

Date Code Title Description
AS Assignment

Owner name: CHASE MANHATTAN BANK, THE NATIONAL ASSOCIATION

Free format text: SECURITY INTEREST;ASSIGNOR:DORSET INC. A CORP OF DELAWARE;REEL/FRAME:005122/0370

Effective date: 19890329

AS Assignment

Owner name: GAF CHEMICALS CORPORATION

Free format text: CHANGE OF NAME;ASSIGNOR:DORSET INC.;REEL/FRAME:005251/0071

Effective date: 19890411

AS Assignment

Owner name: RHONE-POULENC SPECIALTY CHEMICALS, L.P., NEW JERSE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:GAF CHEMICALS CORPORATION;REEL/FRAME:005315/0588

Effective date: 19900404

AS Assignment

Owner name: DORSET INC., A DE CORP.

Free format text: CHANGE OF NAME;ASSIGNOR:GAF CORPORATION, A DE CORP.;REEL/FRAME:005250/0940

Effective date: 19890410

AS Assignment

Owner name: DORSET INC.,

Free format text: RELEASED BY SECURED PARTY;ASSIGNOR:CHASE MANHATTAN BANK, THE,;REEL/FRAME:005597/0269

Effective date: 19890329

AS Assignment

Owner name: RHONE - POULENC SPECIALITY CHEMICALS

Free format text: A CORRECTIVE ASSIGNMENT TO CORRECT THE SINGLE SERIAL NUMBER 07194,259 IDENTIFIED IN PREVIOUSLY RECORDED ASSIGMENT ON REEL 5315/FRAME 589.;ASSIGNOR:GAF CHEMICALS CORPORATION;REEL/FRAME:005722/0439

Effective date: 19910513

AS Assignment

Owner name: RHONE-POULENC SURFACTANTS AND SPECIALTIES INC., NE

Free format text: CHANGE OF NAME;ASSIGNOR:RHONE-POULENC SPECIALTY CHEMICALS INC.;REEL/FRAME:005748/0167

Effective date: 19910123

Owner name: RHONE-POULENC SURFACTANTS AND SPECIALTIES, L.P.

Free format text: CHANGE OF NAME;ASSIGNOR:RHONE-POULENC SPECIALTY CHEMICALS, L.P.;REEL/FRAME:005753/0422

Effective date: 19900430