US2967829A - Stabilized liquid petroleum lubricant - Google Patents

Stabilized liquid petroleum lubricant Download PDF

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US2967829A
US2967829A US744925A US74492558A US2967829A US 2967829 A US2967829 A US 2967829A US 744925 A US744925 A US 744925A US 74492558 A US74492558 A US 74492558A US 2967829 A US2967829 A US 2967829A
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liquid petroleum
nitro
petroleum
nitroester
stabilized liquid
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Edward O Bennett
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Commercial Solvents Corp
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • 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
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/14Synthetic waxes, e.g. polythene waxes
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16Paraffin waxes; Petrolatum, e.g. slack wax
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/17Fisher Tropsch reaction products
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix 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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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    • C10M2207/00Organic 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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/18Tall oil acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/22Acids obtained from polymerised unsaturated acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
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    • C10M2207/40Fatty vegetable or animal oils
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/404Fatty vegetable or animal oils obtained from genetically modified species
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/10Amides of carbonic or haloformic acids
    • C10M2215/102Ureas; Semicarbazides; Allophanates
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/20Containing nitrogen-to-oxygen bonds
    • C10M2215/202Containing nitrogen-to-oxygen bonds containing nitro groups
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    • 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
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/22Metal working with essential removal of material, e.g. cutting, grinding or drilling
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/30Refrigerators lubricants or compressors lubricants
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/32Wires, ropes or cables lubricants
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    • C10N2040/34Lubricating-sealants
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/36Release agents or mold release agents
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    • C10N2040/38Conveyors or chain belts
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    • C10N2040/40Generators or electric motors in oil or gas winning field
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    • C10N2040/42Flashing oils or marking oils
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    • C10N2040/50Medical uses

Definitions

  • My invention relates to a stabilized petroleum lubricant and more particularly to a process for the production of stabilized petroleum lubricants containing as the active stabilizing agent nitroesters having the structural formula:
  • B A-R R is selected from the group consisting of hydrogen, halo, methyl, ethyl and propyl; R is selected from the group consisting of methyl, ethyl, propyl and acyloxyalkyl with the proviso that at least one acyloxyalkyl radical is present; wherein the acyloxy and alkyl radicals contain 1-3 carbon atoms each.
  • my active ingredients are effective bacteriostatic agents in petroleum containing lubricants such as cutting oils, penetrating oils, grinding lubricants, iron tinning lubricants, core oils, hydraulic fluids, etc.
  • Example I My active ingredients were tested in a 25:1 water-cutting oil emulsion.
  • the cutting oil concentrate used was a proprietary cutting oil containing no bacterial inhibitors States Patent hce sold by the Texas Company under the trade name Soluble Oil TL-3337.
  • Six 3000 ml. portions of the water-cutting oil emulsion were placed in large mouthed one gallon glass containers. Desired amounts of my nitroesters were added to the cutting oil emulsion. No inhibitor was added to one 3000 ml. portion of the cutting oil emulsion which was used as a control. At the beginning of the experiment each unit was inoculated with 5 mls.
  • Example [I The following is a water emulsifiable cutting oil which is adequately protected by 1000 parts per million'of my nitroester inhibitors.
  • Example 111 The following is a stabilized steam cylinder oil which is adequately protected by 100 parts per million-of 2-nitro- 2-bromo-1-propylacetate.
  • Example IV Percent S.A.E. lubricating oil Oleic acid 10
  • Example IV The following is a core oil which is adequately protected by 1000 parts per million of 2-nitro-2-methyl-l-propylacetate.
  • Example V The following is a cutting oil which is adequately protected by 1000 parts per million of 2-nitro-2ethyl-1,3- propanediol dipropionate.
  • a liquid petroleum lubricant composition consisting essentially of a liquid petroleum hydrocarbon and a suflicient amount of a nitroester to stabilize said hydrocarbon wherein R is selected from the group consisting of hydrogen, halo, methyl, ethyl, and propyl; R is selected from the group consisting of methyl, ethyl, propyl, and acyloxyalkyl with the proviso that at least one acyloxyalkyl radical is present; wherein the acyloxyl and alkyl radicals contain 1 to 3 carbon atoms each.
  • composition of claim 1 wherein the compound is 2-nitro-2-bromo-1-propylacetatc.
  • composition of claim 1 wherein the compound is 2-nitro-2-ethyl-1,3-propanediol dipropionate.
  • composition of claim 1 wherein the compound is 2-nitro-2-chloro-1,3-propanediol diacetate.
  • composition of claim 1 wherein the compound is 2-nitro-2-methyl-l-propylacetate.
  • a liquid petroleum lubricant composition consisting essentially of a liquid petroleum hydrocarbon and more than 100 ppm. of a nitroester to stabilize said hydro- 4 carbon against metabolizing bacteria, said nitroester having the following structural formula:
  • R is selected from the group consisting of hydrogen, halo, methyl, ethyl, and propyl; R is selected from the group consisting of methyl, ethyl, propyl, and acyloxyalkyl with the proviso that at least one acyloxy radical is present; wherein the acyloxy and alkyl radicals contain 1 to 3 carbon atoms each.

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  • 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)
  • Lubricants (AREA)

Description

2,967,829 STABILIZED LIQUID PETROLEUM LUBRICANT Edward 0. Bennett, Houston, Tex., assignor to Commercial Solvents Corporation, Terre Haute, Ind., a corporation of Maryland No Drawing. Filed June 27, 1958, Ser. No. 744,925
6 Claims. (Cl. 252-515) My invention relates to a stabilized petroleum lubricant and more particularly to a process for the production of stabilized petroleum lubricants containing as the active stabilizing agent nitroesters having the structural formula:
NO, B A-R R is selected from the group consisting of hydrogen, halo, methyl, ethyl and propyl; R is selected from the group consisting of methyl, ethyl, propyl and acyloxyalkyl with the proviso that at least one acyloxyalkyl radical is present; wherein the acyloxy and alkyl radicals contain 1-3 carbon atoms each.
It is well known that organisms from the groups consisting of Corynebacteriurn, Achromobacter, Pseudomona, Nocardia and Mycobacterium metabolize petroleum hydrocarbons and fatty acids and thereby produce undesirable oxidation products.
The petroleum industry has long been interested in the stabilization of various petroleum products such as cutting oils, hydraulic fluids, etc., against breakdown by bacteria which metabolize the hydrocarbons with the concurrent formation of deleterious metabolites.
Many compounds have been used as stabilization agents in lubricants, but very few have been found to be commercially successful due to the fact that the compounds are unstable, or are not active against a wide variety of microorganisms.
Among the compounds included within the scope of my invention are Z-nitro-l-propyl-l-butylformate, 2-nitro- 2-bromo-1-propylacetate, 2-nitro-2-ethyl-1,3-propanediol dipropionate, 2-nitro-2-chloro-1,3-propanediol diacetate, 2-nitro-2-methyl-l-propylacetate, etc. I have found that in some instances I can obtain total inhibition of bacterial growth in petroleum lubricants at concentrations as low as 100 parts per million. I prefer to include at least 1000 parts per million in most petroleum formulations. How- 'ever, I can employ amounts up to 2% by weight of the active nitroesters when the latter is soluble to this extent in the particular petroleum hydrocarbon composition.
I have found that my active ingredients are effective bacteriostatic agents in petroleum containing lubricants such as cutting oils, penetrating oils, grinding lubricants, iron tinning lubricants, core oils, hydraulic fluids, etc.
The following examples set out lubricating compositions in which my active ingredients act as effective bacteriostatic agents. It is not intended that my invention be limited to the compositions, portions, or lubricants set out below, but rather I intend for all equivalents and varia tions obvious to those skilled in the art to be included within the scope of this specification and the attached claims.
Example I My active ingredients were tested in a 25:1 water-cutting oil emulsion. The cutting oil concentrate used was a proprietary cutting oil containing no bacterial inhibitors States Patent hce sold by the Texas Company under the trade name Soluble Oil TL-3337. Six 3000 ml. portions of the water-cutting oil emulsion were placed in large mouthed one gallon glass containers. Desired amounts of my nitroesters were added to the cutting oil emulsion. No inhibitor was added to one 3000 ml. portion of the cutting oil emulsion which was used as a control. At the beginning of the experiment each unit was inoculated with 5 mls. of a heterogeneous bacterial culture which had grown for several years in a water-cutting oil emulsion. Aeration and mixing were obtained by bubbling compressed air through the emulsion. Water was added to each portion of the emulsion at periodic intervals in order to keep the volume of the units constant and to prevent concentration of the inhibitor by evaporation.
The following table sets out the results from the above tests and the number of days of total bacterial inhibition when the described concentration of the desired nitroester was incorporated into the cutting oil emulsion.
Example [I The following is a water emulsifiable cutting oil which is adequately protected by 1000 parts per million'of my nitroester inhibitors.
Light mineral oil Percent by weight" Oleic acid percent 10 Example 111 The following is a stabilized steam cylinder oil which is adequately protected by 100 parts per million-of 2-nitro- 2-bromo-1-propylacetate.
Percent S.A.E. lubricating oil Oleic acid 10 Example IV The following is a core oil which is adequately protected by 1000 parts per million of 2-nitro-2-methyl-l-propylacetate.
Percent Crude tall oil 25 Fuel oil 35 Tall oil ester (glycol or glycerol) 40 Example V The following is a cutting oil which is adequately protected by 1000 parts per million of 2-nitro-2ethyl-1,3- propanediol dipropionate.
Percent Tallow 65 Parafiin wax 29 Bees wax 1.3 Oxalic acid 1.3 Potassium citrate 1.3 Urea 0.4
Now having described my invention what I claim is:
1. A liquid petroleum lubricant composition consisting essentially of a liquid petroleum hydrocarbon and a suflicient amount of a nitroester to stabilize said hydrocarbon wherein R is selected from the group consisting of hydrogen, halo, methyl, ethyl, and propyl; R is selected from the group consisting of methyl, ethyl, propyl, and acyloxyalkyl with the proviso that at least one acyloxyalkyl radical is present; wherein the acyloxyl and alkyl radicals contain 1 to 3 carbon atoms each.
2. The composition of claim 1 wherein the compound is 2-nitro-2-bromo-1-propylacetatc.
3. The composition of claim 1 wherein the compound is 2-nitro-2-ethyl-1,3-propanediol dipropionate.
4. The composition of claim 1 wherein the compound is 2-nitro-2-chloro-1,3-propanediol diacetate.
5. The composition of claim 1 wherein the compound is 2-nitro-2-methyl-l-propylacetate.
6. A liquid petroleum lubricant composition consisting essentially of a liquid petroleum hydrocarbon and more than 100 ppm. of a nitroester to stabilize said hydro- 4 carbon against metabolizing bacteria, said nitroester having the following structural formula:
wherein R is selected from the group consisting of hydrogen, halo, methyl, ethyl, and propyl; R is selected from the group consisting of methyl, ethyl, propyl, and acyloxyalkyl with the proviso that at least one acyloxy radical is present; wherein the acyloxy and alkyl radicals contain 1 to 3 carbon atoms each.
References Cited in the file of this patent UNITED STATES PATENTS 1,502,174 Chapman July 22, 1924 2,427,821 Tindall Sept. 23, 1947 2,581,120 Matuszak Jan. 1, 1952 2,763,962 Hardy Sept. 25, 1956 OTHER REFERENCES Lubrication Eng, March 1957, pages 151-153.

Claims (1)

1. A LIQUID PETROLEUM LUBRICANT COMPOSITION CONSISTING ESSENTIALLY OF A LIQUID PETROLEUM HYDROCARBON AND A SUFFICIENT AMOUNT OF A NITROESTER TO STABILIZE AID HYDROCARBON AGAINST METABOLIZING BACTERIA, SAID NITROESTER HAVING THE FOLLOWING STRUCTURAL FORMULA:
US744925A 1958-06-27 1958-06-27 Stabilized liquid petroleum lubricant Expired - Lifetime US2967829A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3513243A (en) * 1963-11-26 1970-05-19 Aerojet General Co New antibiotic and fungicidal agents
US4469703A (en) * 1979-07-26 1984-09-04 Egyt Gyogyszervegyeszeti Gyar Nitroalkanol derivatives and plant protecting agents containing the same

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1502174A (en) * 1923-12-15 1924-07-22 Chapman Royal Norton Fumigant
US2427821A (en) * 1944-01-22 1947-09-23 Commercial Solvents Corp Higher esters of chloro nitro alcohols
US2581120A (en) * 1948-05-05 1952-01-01 Standard Oil Dev Co Rust inhibiting composition
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US1502174A (en) * 1923-12-15 1924-07-22 Chapman Royal Norton Fumigant
US2427821A (en) * 1944-01-22 1947-09-23 Commercial Solvents Corp Higher esters of chloro nitro alcohols
US2581120A (en) * 1948-05-05 1952-01-01 Standard Oil Dev Co Rust inhibiting composition
US2763962A (en) * 1952-12-24 1956-09-25 Dow Chemical Co Fungicidal fumigant composition comprising bromonitromethane and method of applying to soil

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3513243A (en) * 1963-11-26 1970-05-19 Aerojet General Co New antibiotic and fungicidal agents
US4469703A (en) * 1979-07-26 1984-09-04 Egyt Gyogyszervegyeszeti Gyar Nitroalkanol derivatives and plant protecting agents containing the same

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