US2875072A - Rust preventative compositions - Google Patents

Rust preventative compositions Download PDF

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US2875072A
US2875072A US2875072DA US2875072A US 2875072 A US2875072 A US 2875072A US 2875072D A US2875072D A US 2875072DA US 2875072 A US2875072 A US 2875072A
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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
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • 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
    • 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
    • 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
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/141Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings monocarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/142Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings 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
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/144Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings containing 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/146Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings having carboxyl groups bound to carbon atoms of six-membeered aromatic rings having a hydrocarbon substituent 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • 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

  • a higher aliphatic primary amine with an aromatic acid e. g., benzoic acid
  • Zinc naph when used in conjunction with Zinc naph thenate in mineral oil provides an unusually eifective corrosion and rust inhibiting composition.
  • the ingredients have sufficient solubility in light hydrocarbon oils for use in sufiicient concentration for practical applications.
  • the amine of choice is a branched chain C to C primary amine in which the hydrocarbon chain is derived from propylene tetramer or a light isobutylene polymer. Such amines are available commercially, for example, Primene J. M. R. amine of Rohm & Haas.
  • Benzoic acid is particularly valuable as the aromatic acid component in the invention, but other aromatic acids possess useful rust inhibiting properties, e. g. salicyclic, phthalic, toluic and cinnamic acids.
  • the amine-aromatic acid combination may be preformed as the amine salt of the acid and dissolved in the hydrocarbon oil base for the rust preventative composition, or the amine and aromatic acid components can be added separately to the base oil so that the product is formed in situ. In either case, we have found that the desired proportion of the amine-aromatic acid product is suitably in the range of about 8 to about 12% by weight.
  • the zinc naphthenates employed are Zinc soaps of naphthenic acid, i. e., the C to C cyclic acids averaging about 150 to 250 in molecular weight which are recovered from naphthenic type crudes by caustic washing.
  • the products commercially available are variable in zinc content and usually contain about 8 to 14% zinc.
  • About 14 to about 28% by weight of zinc naphthenate, based on a concentration of zinc of about 8% by weight, may be used in formulating the compositions of the invention.
  • the base oil may comprise a light lubricating oil distillate, e. g. a neutral oil, with advantage. Heavier lubricating oil fractions, however, may be used and kerosene or various light hydrocarbon solvents may be used to cut the finished compositions back to the desired viscosity for convenient application by dipping, spraying Patented F eb. 24, 1959 or brushing.
  • a particularly well balanced formulation may contain about 8 to 12% of the amine-'benzoate product, about 20 to 28% of zinc naphthenate (8% Zn), about 50 to of a lubricating oil of 60 to .100 SSU at F., and about 12 to 20% of a solvent naphtha such as Stoddards solvent.
  • the speciments were then placed in a dessicator which was prepared in the following manner One hundred ml. of 5% acetic acid solution was placed in a 100 ml. beaker which in turn was placed in a crystallization dish 2" high by 4" diameter The dish was filled with water and the assembly placed in the bottom of the dessicator.
  • the porcelain table was supported on its edges with corks in the dessicator to raise it above the beaker containing the acid.
  • the crucible and balls were set on this porcelain table and the cover to the dessicator put in place.
  • the test was run at room temperature, and the ball bearings were checked daily for presence of rust.
  • the amine used was Primene J. M. R. which is a mixture of tertiary alkyl primary amines predominating in C H NH but ranging up to C H NH Physical tests on the amine included: 5-70% over at 262 to 315 C., specific gravity at 25 C. of 0.845, refractive index at 25 C. of 1.460 and flash point of 260 F.
  • the amine: and benzoic acid were separately incorporated in the base oil, and the mixture was stirred at F. until no crystals remained in solution.
  • the amine-benzoate product was formed by combining one mole of the amine with two moles of acid. The materials were stirred and heated at 150 F. for a few minutes at which point the addition of benzoic acid to the amine was complete. The resultant product was a honey-like material in consistency and odor.
  • temperatures of about 200 F. or more are to be avoided since at that temperature, water is eliminated and the amide is formed.
  • phatic primary amine containing about 18 to 24 carbon References Cited in the file of mi a n atoms and an aromatic acid, and about 14 to about 28% s p m t f Zinc naphthenate.
  • UNITED STATES PATENTS 2.
  • the composition of claim 1 in which the amine is 2,333,206 Sloan Nov. 2, 1943 a C to C aliphatic branched chain primary amine. 2,401,993 Wasson et al June 11, 1946 3.
  • the composition of claim 1 in which the acid is 2,415,353 Johnston et al. Feb. 4, 1947 benzolc acid. 2,587,777 Smith Mar. 4, 1952 4.
  • a rust preventative composition of the slushing oil 2,615,815 Galvin et a1. Oct. 28, 1952 type characterized by capacity for protecting metal sur- 0 2,629,649

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

Description

Edgar A. Dieman,
UnitedStates Patent I O 2,875,072 Rnsr PREVENTATIYE COMPOSITIONS Crown Point, and James W. Gaynor, Valparaiso, Ind., assignors to Standard Oil Company, Chicago, 111., a corporation of Indiana No Drawing. Application June 29, 1955 Serial No. 518,978
4 Claims. (Cl. 106-14) Our invention relates .to rust preventative compositions, of the slashing oil type, which have particular value for protecting metal surfaces in acid atmospheres.
Various organic acids have been proposed for use in oil compositions for preventing rusting of metal surfaces in acid atmospheres. Although aromatic acids have considerable effectiveness, their practical effectiveness is substantially reduced by their relative insolubility in hydrocarbon oils. Efforts have been made to solubilize such materials to an extent permitting practical utilization wit out interfering with or reducing their rust inhibiting capacities. This, however, has proved difiicult to accomplish and, accordingly, it is an object of our invention to provide a rust preventative composition of improved properties for use in acid atmospheres.
We have found that the combination of a higher aliphatic primary amine with an aromatic acid, e. g., benzoic acid, when used in conjunction with Zinc naph thenate in mineral oil provides an unusually eifective corrosion and rust inhibiting composition. The ingredients have sufficient solubility in light hydrocarbon oils for use in sufiicient concentration for practical applications. The amine of choice is a branched chain C to C primary amine in which the hydrocarbon chain is derived from propylene tetramer or a light isobutylene polymer. Such amines are available commercially, for example, Primene J. M. R. amine of Rohm & Haas.
Other high aliphatic primary amines, however, may be used as long as the resultant product is soluble in oil. Thus, primary amines containing long, usually branched, chains of C to C in length have value.
Benzoic acid is particularly valuable as the aromatic acid component in the invention, but other aromatic acids possess useful rust inhibiting properties, e. g. salicyclic, phthalic, toluic and cinnamic acids. The amine-aromatic acid combination may be preformed as the amine salt of the acid and dissolved in the hydrocarbon oil base for the rust preventative composition, or the amine and aromatic acid components can be added separately to the base oil so that the product is formed in situ. In either case, we have found that the desired proportion of the amine-aromatic acid product is suitably in the range of about 8 to about 12% by weight.
The zinc naphthenates employed are Zinc soaps of naphthenic acid, i. e., the C to C cyclic acids averaging about 150 to 250 in molecular weight which are recovered from naphthenic type crudes by caustic washing. The products commercially available are variable in zinc content and usually contain about 8 to 14% zinc. About 14 to about 28% by weight of zinc naphthenate, based on a concentration of zinc of about 8% by weight, may be used in formulating the compositions of the invention.
The base oil may comprise a light lubricating oil distillate, e. g. a neutral oil, with advantage. Heavier lubricating oil fractions, however, may be used and kerosene or various light hydrocarbon solvents may be used to cut the finished compositions back to the desired viscosity for convenient application by dipping, spraying Patented F eb. 24, 1959 or brushing. A particularly well balanced formulation may contain about 8 to 12% of the amine-'benzoate product, about 20 to 28% of zinc naphthenate (8% Zn), about 50 to of a lubricating oil of 60 to .100 SSU at F., and about 12 to 20% of a solvent naphtha such as Stoddards solvent.
In evaluating the compositions of the invention, rep resentative samples were formulated and tested by means of a specially devised corrosion test .for rating performance of rust inhibitors in strongly acid atmospheres. The procedure was conducted as follows: Three steel :ball bearings were placed in .a gooch crucible 1" high by 1% diameter at the bottom. The crucible and ball bearings were slushed for one minute in hot naphtha to remove foreign material. The crucible and ball bearings were set on an absorbent paper for about /2 hour to allow cooling to room temperature and evaporation of the solvent. These were then slushed for one minute in the rust preventive compound and allowed to drain .for two hours on a fresh piece of absorbent paper. The speciments were then placed in a dessicator which was prepared in the following manner One hundred ml. of 5% acetic acid solution was placed in a 100 ml. beaker which in turn was placed in a crystallization dish 2" high by 4" diameter The dish was filled with water and the assembly placed in the bottom of the dessicator. The porcelain table was supported on its edges with corks in the dessicator to raise it above the beaker containing the acid. The crucible and balls were set on this porcelain table and the cover to the dessicator put in place. The test was run at room temperature, and the ball bearings were checked daily for presence of rust.
In the following examples, the amine used was Primene J. M. R. which is a mixture of tertiary alkyl primary amines predominating in C H NH but ranging up to C H NH Physical tests on the amine included: 5-70% over at 262 to 315 C., specific gravity at 25 C. of 0.845, refractive index at 25 C. of 1.460 and flash point of 260 F.
In one method of preparation, the amine: and benzoic acid were separately incorporated in the base oil, and the mixture was stirred at F. until no crystals remained in solution. In a second method of preparation, the amine-benzoate product was formed by combining one mole of the amine with two moles of acid. The materials were stirred and heated at 150 F. for a few minutes at which point the addition of benzoic acid to the amine was complete. The resultant product was a honey-like material in consistency and odor. In preparing the additive product, temperatures of about 200 F. or more are to be avoided since at that temperature, water is eliminated and the amide is formed.
The data of Table I below indicate by comparison the superiority of compositions of the invention containing the amine-benzoate additive when used in conjunction with greater than about 12-16% by weight of zinc naphthenate. It will be noted that zinc naphthenate alone is ineffective in inhibiting rusting of steel in acid atmospheres. Although the formulation made without use of an amine showed activity, the sample had to be applied carefully as a suspension. The additives in the test did not remain in solution, and such formulations lack prac' tical utility. Use of the amine-benzoic acid combina tion, however, Whether preformed or produced in situ in the base oil, eliminates the problem of solubility en countered with the use of the acid alone while providing a significantly superior rust preventative composition. When low percentages of the amine-acid combination are used, the inhibiting effectiveness of the composition is markedly reduced. See, for example, sample 6. At least about 8% of the additive product should be used for satisfactory results.
Table 1 Zn Naphthenate (14.5% Zn) 26.3 o 0 o 24 0 0 o 0 Zn Naphthenate (Nuodex 8% Zn) 0 4 12 16 24 0 24 24 24 24 Pale on. so ssU at 100 o 70 e2 54 50 50 55 55. a 50 50 White 011 50 0 o 0 0 o 0 0 e r 0 0 Solvent Naphtha. 15. 15 1c 16 16 15 1c 16 16 16 Sodium Sulionato 2. 5 0 0 0 0 o 0 0 0 o Prlmenc J. M. R. o 5.25 5.25 5. 25 5.25 5. 25 2.62 0 0 0 Benzoic Acid 4.7 4.75 4. 75 4.75 4. 75 4.75 2.38 4.7 0 0 Primene-Benzoic Acid Product 0 0 0 0 0 0 0 0 0 Appearance Prectipticlear clear clear clear clear clear Preciigti a clear clear a e 1 Days to rust in Acid Atmospheres. 14 7 14 i 21 18 3 14 3 1 All proportions are percent by weight of the total composition. 7 We claim: faces in acid atmospheres consisting essentially of a lubri- 1. A rust preventative composition of the slashing oil eating oil distillate as base and containing dissolved type characterized by capacity for protecting metal surtherein about 8 to about 12% in combination of a C faces in acid atmospheres consisting essentially of a hyto C aliphatic branched chain primary amine and bendrocarbon oil as base and containing dissolved therein zoic acid, about 14 to about 28% of zinc naphthenate about 8 to about 12% in combination of a higher aliand about 12 to about 20% of a solvent naphtha. phatic primary amine containing about 18 to 24 carbon References Cited in the file of mi a n atoms and an aromatic acid, and about 14 to about 28% s p m t f Zinc naphthenate. UNITED STATES PATENTS 2. The composition of claim 1 in which the amine is 2,333,206 Sloan Nov. 2, 1943 a C to C aliphatic branched chain primary amine. 2,401,993 Wasson et al June 11, 1946 3. The composition of claim 1 in which the acid is 2,415,353 Johnston et al. Feb. 4, 1947 benzolc acid. 2,587,777 Smith Mar. 4, 1952 4. A rust preventative composition of the slushing oil 2,615,815 Galvin et a1. Oct. 28, 1952 type characterized by capacity for protecting metal sur- 0 2,629,649
Wachter et al. Feb. 24, 1953

Claims (1)

1. A RUST PREVENTATIVE COMPOSITION OF THE SLUSHING OIL TYPE CHARACTERIZED BY CAPACITY FOR PROJECTING METAL SURFACES IN ACID ATMOSPHERES CONSISTING ESSENTIALLY OF A HYDROCARBON OIL AS BASE AND CONTAINING DISSOLVED THEREIN ABOUT 8 TO ABOUT 12% IN COMBINATION OF A HIGHER ALIPHATIC PRIMARY AMINE CONTAINING ABOUT 18 TO 24 CARBON ATOMS AND AN AROMATIC ACID, AND ABOUT 14 TO ABOUT 28% OF ZINC NAPHTHENATE.
US2875072D Rust preventative compositions Expired - Lifetime US2875072A (en)

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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2333206A (en) * 1939-05-13 1943-11-02 Du Pont Protection of ferrous metals against corrosion
US2401993A (en) * 1942-12-31 1946-06-11 Standard Oil Dev Co Corrosion resistant composition
US2415353A (en) * 1944-03-15 1947-02-04 Standard Oil Dev Co Rust preventing turbine oil
US2587777A (en) * 1947-04-30 1952-03-04 Detrex Corp Cleaning and rustproofing composition
US2615815A (en) * 1948-03-12 1952-10-28 Shell Dev Corrosion inhibiting composition
US2629649A (en) * 1949-10-31 1953-02-24 Shell Dev Vapor-phase corrosion inhibitor

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2333206A (en) * 1939-05-13 1943-11-02 Du Pont Protection of ferrous metals against corrosion
US2401993A (en) * 1942-12-31 1946-06-11 Standard Oil Dev Co Corrosion resistant composition
US2415353A (en) * 1944-03-15 1947-02-04 Standard Oil Dev Co Rust preventing turbine oil
US2587777A (en) * 1947-04-30 1952-03-04 Detrex Corp Cleaning and rustproofing composition
US2615815A (en) * 1948-03-12 1952-10-28 Shell Dev Corrosion inhibiting composition
US2629649A (en) * 1949-10-31 1953-02-24 Shell Dev Vapor-phase corrosion inhibitor

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