US2323670A - Lubricating oil, etc. - Google Patents
Lubricating oil, etc. Download PDFInfo
- Publication number
- US2323670A US2323670A US358930A US35893040A US2323670A US 2323670 A US2323670 A US 2323670A US 358930 A US358930 A US 358930A US 35893040 A US35893040 A US 35893040A US 2323670 A US2323670 A US 2323670A
- Authority
- US
- United States
- Prior art keywords
- methane
- tetra
- sulphate
- alkyl
- phenyl
- 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
Links
- 239000010687 lubricating oil Substances 0.000 title description 2
- -1 alkyl sulphuric Chemical compound 0.000 description 10
- 239000003921 oil Substances 0.000 description 7
- 239000002480 mineral oil Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical class CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- 239000004141 Sodium laurylsulphate Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 3
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- JNRLEMMIVRBKJE-UHFFFAOYSA-N 4,4'-Methylenebis(N,N-dimethylaniline) Chemical compound C1=CC(N(C)C)=CC=C1CC1=CC=C(N(C)C)C=C1 JNRLEMMIVRBKJE-UHFFFAOYSA-N 0.000 description 2
- WZKXBGJNNCGHIC-UHFFFAOYSA-N Leucomalachite green Chemical compound C1=CC(N(C)C)=CC=C1C(C=1C=CC(=CC=1)N(C)C)C1=CC=CC=C1 WZKXBGJNNCGHIC-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- ZWGWPHTUOWMLHG-UHFFFAOYSA-N phenyl-(2,3,4,5-tetraethylphenyl)methanediamine Chemical compound CCC1=C(CC)C(CC)=CC(C(N)(N)C=2C=CC=CC=2)=C1CC ZWGWPHTUOWMLHG-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- JJVGLYUEASMKDD-UHFFFAOYSA-N 4-benzylbenzene-1,2,3-triamine Chemical compound NC1=C(C(=C(C=C1)CC1=CC=CC=C1)N)N JJVGLYUEASMKDD-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-O Methylammonium ion Chemical compound [NH3+]C BAVYZALUXZFZLV-UHFFFAOYSA-O 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- GDWRXJCWAANTID-UHFFFAOYSA-N azanium;hexyl sulfate Chemical compound [NH4+].CCCCCCOS([O-])(=O)=O GDWRXJCWAANTID-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- QTPSOVJLZXSTEB-UHFFFAOYSA-L calcium;dodecyl sulfate Chemical compound [Ca+2].CCCCCCCCCCCCOS([O-])(=O)=O.CCCCCCCCCCCCOS([O-])(=O)=O QTPSOVJLZXSTEB-UHFFFAOYSA-L 0.000 description 1
- HNDVCIKSNWLJHQ-UHFFFAOYSA-L calcium;octane-1-sulfonate Chemical compound [Ca+2].CCCCCCCCS([O-])(=O)=O.CCCCCCCCS([O-])(=O)=O HNDVCIKSNWLJHQ-UHFFFAOYSA-L 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- MGHPNCMVUAKAIE-UHFFFAOYSA-N diphenylmethanamine Chemical compound C=1C=CC=CC=1C(N)C1=CC=CC=C1 MGHPNCMVUAKAIE-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- HBNDBUATLJAUQM-UHFFFAOYSA-L magnesium;dodecyl sulfate Chemical compound [Mg+2].CCCCCCCCCCCCOS([O-])(=O)=O.CCCCCCCCCCCCOS([O-])(=O)=O HBNDBUATLJAUQM-UHFFFAOYSA-L 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 230000000116 mitigating effect Effects 0.000 description 1
- UZZYXUGECOQHPU-UHFFFAOYSA-N octyl hydrogen sulfate Chemical compound CCCCCCCCOS(O)(=O)=O UZZYXUGECOQHPU-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- DYFXGORUJGZJCA-UHFFFAOYSA-N phenylmethanediamine Chemical class NC(N)C1=CC=CC=C1 DYFXGORUJGZJCA-UHFFFAOYSA-N 0.000 description 1
- MEGDIQXLXPPWGL-UHFFFAOYSA-N phenylmethanetriamine Chemical class NC(N)(N)C1=CC=CC=C1 MEGDIQXLXPPWGL-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/067—Polyaryl amine alkanes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/042—Sulfate esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/06—Groups 3 or 13
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/08—Groups 4 or 14
Definitions
- the oil may be of various character and source, and for instance may be of viscosity 45 to 200 sec. Saybolt Universal at 210 F., and of Mid- Continent or other source.
- a phenyl methane derivative and a salt of an oxy-sulphur acid i. e. alkyl sulphuric or sulphonic acid of the general formula R.SO1L.R', wherein R'is an alkyl or halogen-substituted alkyl radical, n is 3 or 4, and R is a base (e. g. lead, tin, aluminum, magnesium or alkaline earth metal, sodium or alkali metal, ammonia or an amine).
- the alkyl sulphuric acid salts are particularly advantageous. Mixtures of alkyl sulphates and sulphonates may be employed, and mixtures are particularly easily had in practice.
- the compounds derivable from cocoanut oil fatty acids by separation and reduction and sulphonation are especially desirable, and of these the lauryl compounds are outstanding.
- the amount of the phenyl methane derivative may be .01 per cent to 2.0 per cent and the alkyl salt 0.1 per cent to 1.0 per cent, depending upon the oil and the particular usage in view.
- phenyl methanes are diamino phenyl methanes, triamino phenyl methanes, as tetra methyl diamino diphenyl methane, tetra ethyl diamino diphenyl methane, tetra benzyl diamino diphenyl methane, tetra-methyl triamino diphenyl methane, tetra amino diphenyl methane, tetra methyl diamino triphenyl methane, tetra ethyl diamino is the maximum with difdrfiary oil.
- triphenyl methane, etc. and illustrative of the alkyl salts are aluminum octyl sulphate, sodium lauryl sulphate, ammonium hexyl sulphate, lead lauryl sulphate, magnesium lauryl sulphate, amyl ammonium cetyl sulphate, methyl ammonium ricinoleo sulphate, calcium lauryl sulphate, etc.
- the alkyl salts are aluminum octyl sulphate, sodium lauryl sulphate, ammonium hexyl sulphate, lead lauryl sulphate, magnesium lauryl sulphate, amyl ammonium cetyl sulphate, methyl ammonium ricinoleo sulphate, calcium lauryl sulphate, etc.
- the alkyl salts are aluminum octyl sulphate, sodium lauryl sulphate, ammonium he
- the combinations involve such a phenyl methane derivative and a salt of alkyl sulphuric or sulphonic acid, as for instance tetra ethyl diamino diphenyl methane and sodium lauryl sulphate, tetra benzyl diamino diphenyl methane and calcium octyl sulphonate, tetra methyl triamino diphenyl methane and'aluminum lauryl sulphate, tetra methyl diamino triphenyl methane and sodium lauryl sulphate, etc.
- alkyl sulphuric or sulphonic acid as for instance tetra ethyl diamino diphenyl methane and sodium lauryl sulphate, tetra benzyl diamino diphenyl methane and calcium octyl sulphonate, tetra methyl triamino diphen
- the piston rating is on a scale of 10, from 0 which represents the degree of cleanness or lack of accumulation characteristic ainew'piston, while 10 V W
- the demerit rating is the sum of the-"sludge, acid number, piston rating, and one-tenth of the viscosity increase.
- a mineral oil containing a small amount of a phenyl amino methane and an alkyl sulphate 4.
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)
- Lubricants (AREA)
Description
I Patented July 6,1943
to The Standard Oil Company, Cleveland, Ohio, a corporation of Ohio.
' No Drawing. Application September 28, 1940,
Serial-No. 358,930
6 Claims.
Mineral oils subjected to usage in contact with metal surfaces and more or less elevated temperature are prone to. undergo considerable changes in body and also form more or less deposit. Various agents have been proposed and are in use in efforts at mitigation of these tendencies, but quite commonly if some advantage is gained in one respect there is produced some offsetting factor which may bequite disadvantageous under some conditions. I have found that the combinations set forth more in detail here- 1 inafter, have an outstanding utility for oils under drastic usages, and surprisingly, the combinational results are out of all proportion to results with the agents applied individually.
To the accomplishment of the foregoing and related ends, the invention, then, comprises thefeatures hereinafter fully described, and particularly pointed out in the claims, the following description setting forth in detail certain illustrative embodiments of the invention, these being indicative however, of but a few of the various ways in which the principle of the invention may be employed.
Depending upon the particular duty in view, the oil may be of various character and source, and for instance may be of viscosity 45 to 200 sec. Saybolt Universal at 210 F., and of Mid- Continent or other source. With it is incorporated a phenyl methane derivative and a salt of an oxy-sulphur acid, i. e. alkyl sulphuric or sulphonic acid of the general formula R.SO1L.R', wherein R'is an alkyl or halogen-substituted alkyl radical, n is 3 or 4, and R is a base (e. g. lead, tin, aluminum, magnesium or alkaline earth metal, sodium or alkali metal, ammonia or an amine). The alkyl sulphuric acid salts are particularly advantageous. Mixtures of alkyl sulphates and sulphonates may be employed, and mixtures are particularly easily had in practice. The compounds derivable from cocoanut oil fatty acids by separation and reduction and sulphonation are especially desirable, and of these the lauryl compounds are outstanding. The amount of the phenyl methane derivative may be .01 per cent to 2.0 per cent and the alkyl salt 0.1 per cent to 1.0 per cent, depending upon the oil and the particular usage in view. Illustrative of the phenyl methanes are diamino phenyl methanes, triamino phenyl methanes, as tetra methyl diamino diphenyl methane, tetra ethyl diamino diphenyl methane, tetra benzyl diamino diphenyl methane, tetra-methyl triamino diphenyl methane, tetra amino diphenyl methane, tetra methyl diamino triphenyl methane, tetra ethyl diamino is the maximum with difdrfiary oil.
'phate.
triphenyl methane, etc., and illustrative of the alkyl salts are aluminum octyl sulphate, sodium lauryl sulphate, ammonium hexyl sulphate, lead lauryl sulphate, magnesium lauryl sulphate, amyl ammonium cetyl sulphate, methyl ammonium ricinoleo sulphate, calcium lauryl sulphate, etc. Correspondingly also the sulphonates. And, the combinations involve such a phenyl methane derivative and a salt of alkyl sulphuric or sulphonic acid, as for instance tetra ethyl diamino diphenyl methane and sodium lauryl sulphate, tetra benzyl diamino diphenyl methane and calcium octyl sulphonate, tetra methyl triamino diphenyl methane and'aluminum lauryl sulphate, tetra methyl diamino triphenyl methane and sodium lauryl sulphate, etc.
As an example: With a lubricating oil of S. A. E. 20 Mid-Continent stock there is incorporated 0.25 per cent of tetra methyl diamino diphenyl methane and 0.5 per cent of sodium lauryl sul- This lubricant in an Ethyl Gasoline Corporation test engine running under full load for a twenty hour continuous period, with sump temperature 300 F. and jacket temperature 212"- F., showed a viscosity increase of 133, sludge formation 0.5, lacquer formation 0.00, piston rating 0, and total demerit rating 4.6. (The piston rating is on a scale of 10, from 0 which represents the degree of cleanness or lack of accumulation characteristic ainew'piston, while 10 V W The demerit rating is the sum of the-"sludge, acid number, piston rating, and one-tenth of the viscosity increase.) In contrast, the S. A. E. 20 oil without the additions, run under the same standard conditions, showed a viscosity increase of 413, sludge formation 4.0 per cent, lacquer formation 80.0
Other modes of applying the principle oftheinvention may be employed, change being made as regards the details described, provided the fea- 3. A mineral oil containing a small amount of l triamino diphenyl methane and an octyl sulphate.
4. A mineral oil containing a small amount of a phenyl amino methane and a lauryl sulphate.
5. A mineral oil containing a small amount of a phenyl amino methane and an alkyl sulphate.
6. A mineral oil containing a small amount of a phenyl amino methane and a salt of an ozw-sulphur acid, of the formula R.SOflR', wherein R is an alkyl or halogen-substituted alkyl radical, n is 3 or 4, and R is a metal, ammonia or amine.
JOHN M. MUSSELMAN.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US358930A US2323670A (en) | 1940-09-28 | 1940-09-28 | Lubricating oil, etc. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US358930A US2323670A (en) | 1940-09-28 | 1940-09-28 | Lubricating oil, etc. |
Publications (1)
Publication Number | Publication Date |
---|---|
US2323670A true US2323670A (en) | 1943-07-06 |
Family
ID=23411627
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US358930A Expired - Lifetime US2323670A (en) | 1940-09-28 | 1940-09-28 | Lubricating oil, etc. |
Country Status (1)
Country | Link |
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US (1) | US2323670A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2443026A (en) * | 1946-01-23 | 1948-06-08 | Texas Co | Stabilized grease compositions |
US2452319A (en) * | 1943-12-08 | 1948-10-26 | Texas Co | Rust and oxidation inhibited lubricating compositions |
US2539422A (en) * | 1947-07-23 | 1951-01-30 | Ward Baking Co | Lubricating oil |
-
1940
- 1940-09-28 US US358930A patent/US2323670A/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2452319A (en) * | 1943-12-08 | 1948-10-26 | Texas Co | Rust and oxidation inhibited lubricating compositions |
US2443026A (en) * | 1946-01-23 | 1948-06-08 | Texas Co | Stabilized grease compositions |
US2539422A (en) * | 1947-07-23 | 1951-01-30 | Ward Baking Co | Lubricating oil |
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