US2521395A - Aluminum soap greases - Google Patents
Aluminum soap greases Download PDFInfo
- Publication number
- US2521395A US2521395A US19633A US1963348A US2521395A US 2521395 A US2521395 A US 2521395A US 19633 A US19633 A US 19633A US 1963348 A US1963348 A US 1963348A US 2521395 A US2521395 A US 2521395A
- Authority
- US
- United States
- Prior art keywords
- grease
- aluminum
- soap
- acid
- greases
- 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
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
- C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix 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
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
Definitions
- As a modifier 0.56% iso octyl phenol was added, the soap and modifier being mixed into about 92% of a low cold test mineral oil having a viscosity of 900 to 1000 S. S. U. at 100 F. with addition of a small amount, about 0.25% of a tackiness agent, such as an oil solution of polybutene.
- the following table shows the various characteristics of greases containing different amounts of aluminum soap (aluminum ste'aratm the 'isooctyl phenol structure modifier siderably less in theexamples where the fatty acid was employed.
- the optimum composition covered by this table appears to be that consisting of 3% aluminum steara'te, 0.56% iso-o'ctyl phenol and 1.2% fatty acid.
- Stearic acid may be used as the saturated iat ty acid or various hydrogenated vegetable or fish oil acids which are commercially available maybe employed. lhe optimum quantity of the free or excess fatty acid to be used appears to be in the range of about 10 to 20%, based on the quantity of aluminum soap employed.
- the aluminum soap is preferably aluminum stearate although other substantially saturated aluminum soaps having between 12 and 22 carbon atoms may be used if desired.
- the added or excess acid appears to have a synergisticeifect on the grease modifier (iso-octyl phenol, as in the example given above). For this reason a considerably lesser-quantity of the modifier can be employed than in thecase where no free acid is used.
- the aluminum stearate grease obtained from commercial source C listed in the table above had particularly good structure stability when prepared on a laboratory scale by rapid cooling. It appears to have excellent structure stability even under conditions of high shear and to give Structure stability of aluminum stearate pressure lubricant Aluminum Soap Source A B 7 0 Manufacturing Process Cooler Pan Cooler Pan Cooler Pan Formulation Y Aluminum Stearate percent '7. 00 8. 9. 8. 00 6. 50 Iso-octyl Phenol d0 1. 40 1. 70 l. 60 Tackmess A ent (10---. 0. 25 O. 25 0. 25 O. 25 0. 25 0. 25 Mineral Oil do 91. 35 93. 75 89. 90. 75 90. 15 93. 25
- the fatty acid may be from 1 to 3 times the quantity of the alkyl phenol. Generally speaking, the quantities employed will be between 0.25 and 2.0% for the fatty acid and 0.25 and 1.25% for the alkylated phenol modifier. For greases containing soaps of good commercial quality the range may often be even narrower. Based on the amount of soap used in the grease, the added fatty acid may be from about 10 to 20% by weight. A good over-all formula for the finished lubricant appears to be 5 to 9% by weight of aluminum soap of saturated or substantially saturated fatty acid, for example aluminum stearate, 89 to 94% of mineral lubricating oil of appropriate grade, i. e. of 35 to 1000 S. S. U. viscosity at 210 F.
- the added acid is preferably stearic acid, although the other saturated fatty acids having between 12 and 22 carbon atoms, and mixtures thereof, may be employed.
- the phenol type modifier is preferably an alkylated phenol, particularly iso-octyl phenol, but other phenols such as resorcinol may be used, as described in application Serial No. 638,431 by Beerbower and Zimmer, now Patent No. 2,449,580.
- a tackiness agent also is usually desirable, though not indispensable. It is commonly used in quantities of 0.1 to 0.5% and other conventional additives such as corrosion inhibitors, oxidation inhibitors, extreme pressure agents, and the like, may be employed, as will be understood by those skilled in the art.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19633A US2521395A (en) | 1948-04-07 | 1948-04-07 | Aluminum soap greases |
| FR979281D FR979281A (fr) | 1948-04-07 | 1949-01-19 | Graisse au savon d'aluminium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19633A US2521395A (en) | 1948-04-07 | 1948-04-07 | Aluminum soap greases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2521395A true US2521395A (en) | 1950-09-05 |
Family
ID=21794227
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US19633A Expired - Lifetime US2521395A (en) | 1948-04-07 | 1948-04-07 | Aluminum soap greases |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2521395A (fr) |
| FR (1) | FR979281A (fr) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2675354A (en) * | 1950-05-18 | 1954-04-13 | Stanolind Oil & Gas Co | Method of producing gels |
| US3060120A (en) * | 1956-02-23 | 1962-10-23 | Exxon Research Engineering Co | Lubricating oil compositions |
| US3269947A (en) * | 1962-04-25 | 1966-08-30 | Standard Oil Co | Lubricant grease |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2065857A (en) * | 1933-10-27 | 1936-12-29 | Standard Oil Co | Antileak agent for greases |
| US2264353A (en) * | 1939-02-09 | 1941-12-02 | Standard Oil Dev Co | Lubricant |
| US2365037A (en) * | 1941-10-24 | 1944-12-12 | Standard Oil Dev Co | Process for preparing aluminum soap greases |
| US2380893A (en) * | 1937-11-15 | 1945-07-31 | Standard Oil Dev Co | Lubricating grease composition |
| US2394567A (en) * | 1941-12-17 | 1946-02-12 | Standard Oil Dev Co | Lubricating grease composition |
| US2431453A (en) * | 1944-12-30 | 1947-11-25 | Standard Oil Dev Co | Lubricant manufacture |
| US2449580A (en) * | 1945-12-29 | 1948-09-21 | Standard Oil Dev Co | Lubricating grease composition |
-
1948
- 1948-04-07 US US19633A patent/US2521395A/en not_active Expired - Lifetime
-
1949
- 1949-01-19 FR FR979281D patent/FR979281A/fr not_active Expired
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2065857A (en) * | 1933-10-27 | 1936-12-29 | Standard Oil Co | Antileak agent for greases |
| US2380893A (en) * | 1937-11-15 | 1945-07-31 | Standard Oil Dev Co | Lubricating grease composition |
| US2264353A (en) * | 1939-02-09 | 1941-12-02 | Standard Oil Dev Co | Lubricant |
| US2365037A (en) * | 1941-10-24 | 1944-12-12 | Standard Oil Dev Co | Process for preparing aluminum soap greases |
| US2394567A (en) * | 1941-12-17 | 1946-02-12 | Standard Oil Dev Co | Lubricating grease composition |
| US2431453A (en) * | 1944-12-30 | 1947-11-25 | Standard Oil Dev Co | Lubricant manufacture |
| US2449580A (en) * | 1945-12-29 | 1948-09-21 | Standard Oil Dev Co | Lubricating grease composition |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2675354A (en) * | 1950-05-18 | 1954-04-13 | Stanolind Oil & Gas Co | Method of producing gels |
| US3060120A (en) * | 1956-02-23 | 1962-10-23 | Exxon Research Engineering Co | Lubricating oil compositions |
| US3269947A (en) * | 1962-04-25 | 1966-08-30 | Standard Oil Co | Lubricant grease |
Also Published As
| Publication number | Publication date |
|---|---|
| FR979281A (fr) | 1951-04-24 |
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