US2278762A - Lubricant - Google Patents
Lubricant Download PDFInfo
- Publication number
- US2278762A US2278762A US374133A US37413341A US2278762A US 2278762 A US2278762 A US 2278762A US 374133 A US374133 A US 374133A US 37413341 A US37413341 A US 37413341A US 2278762 A US2278762 A US 2278762A
- Authority
- US
- United States
- Prior art keywords
- oil
- aceto
- lubricant
- oils
- oxidation
- 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
- 239000000314 lubricant Substances 0.000 title description 12
- 239000003921 oil Substances 0.000 description 23
- -1 sulfur heterocyclic compounds Chemical class 0.000 description 12
- 230000003647 oxidation Effects 0.000 description 9
- 238000007254 oxidation reaction Methods 0.000 description 9
- 239000010802 sludge Substances 0.000 description 9
- 150000001412 amines Chemical class 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000010687 lubricating oil Substances 0.000 description 6
- 230000007704 transition Effects 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical group 0.000 description 5
- 125000001145 hydrido group Chemical group *[H] 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000010688 mineral lubricating oil Substances 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000010933 acylation Effects 0.000 description 3
- 238000005917 acylation reaction Methods 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 238000005728 strengthening Methods 0.000 description 2
- GLQWRXYOTXRDNH-UHFFFAOYSA-N thiophen-2-amine Chemical compound NC1=CC=CS1 GLQWRXYOTXRDNH-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- CYKIHIBNSFRKQP-UHFFFAOYSA-N benzo[f][1]benzothiole Chemical compound C1=CC=C2C=C(SC=C3)C3=CC2=C1 CYKIHIBNSFRKQP-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- JCCNYMKQOSZNPW-UHFFFAOYSA-N loratadine Chemical compound C1CN(C(=O)OCC)CCC1=C1C2=NC=CC=C2CCC2=CC(Cl)=CC=C21 JCCNYMKQOSZNPW-UHFFFAOYSA-N 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- GVIJJXMXTUZIOD-UHFFFAOYSA-N thianthrene Chemical compound C1=CC=C2SC3=CC=CC=C3SC2=C1 GVIJJXMXTUZIOD-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- OKYDCMQQLGECPI-UHFFFAOYSA-N thiopyrylium Chemical compound C1=CC=[S+]C=C1 OKYDCMQQLGECPI-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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
-
- 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
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/102—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon only in the ring
-
- 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
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
-
- 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
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/106—Thiadiazoles
-
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
Definitions
- heterocyclic sulfur compounds when added to petroleum oils have little or no benefiial effect upon the oils.
- free .amines of heterocyclic sulfur compounds will decrease the susceptibility of oils to oxidation.
- such amines are usually so unstable toward oxidation and polymerization in themselves as to make their manufacture and use impractical.
- amino thiophene is oxidized and polymerized to an insoluble solid in a few minutes time by light and oxygen.
- the resulting compounds are then relatively stable, and are effective in improving the oiliness or film strength, resistance to oxidation and sludge formation properties of oils.
- An object of this invention is to provide a lubricant having improved properties such as improved oiliness or film strength, a decreased tendency toward corrosiveness, oxidation, and sludge formation.
- An object of this invention is to provide a method for increasing the film strength or oiliness as well as reducing the tendency towards corrosiveness, oxidation and sludge formation of lubricating oils.
- acid amide derivatives of sulfur containing heterocyclic compounds when added to petroleum oils in amounts generally less than 2%, will decrease the susceptibility of such oils to oxidation and sludge formation, as well as increase their film strength or oiliness.
- Such amides, or more specifically acid amides may be prepared by acylation with an organic acid, acid anhydride or acid chloride according to known methods.
- the resulting acid amides are a relatively stable group of compounds and I have found them to be effective in improving the quality of lubricating oils as herein described.
- Aceto thiophenide which is the acetyl derivative of the relatively unstable amino thiophene and acetic acid, is quite stable. This material when added to a lubricating oil materially improves the properties thereof. This improvement in quality of a so treated oil is evidenced by the following example which tabulates results of Stephens consistorneter tests, as follows:
- Example I Saybolt Uni- Transition versal vis Percent aceto tliiophcnide additive point temcosity at perature transition temperature F. Szcondr Oil, no additive 300 39.8 Oil+0.025% additive 311 38. 7 0il+0.05% additive 320 32. 9
- the Stephens consistometer previously manufactured by Stephens Consistome'ter Corporation, 332 South Michigan Avenue, Chicago, Illinois, is a device for use in the testing of lubricants.
- the device consists of two circular metal plates, one of which is rotated at a constant speed, and to the other plate is attached a recording indicator. These two circular plates are immersed in a bath of the lubricant under test, one plate rotated at constant speed and the drag on the second plate indicated by the recorder.
- the oil being tested is warmed slowly and a the temperature increases the drag on the second plate decreases due to the thinning of the oil until a temperature is reached at which the oil film breaks and seizure occurs. This temperature is recorded as the transition point temperature.
- Aceto thiophenide and its hydro-, nitro-, halogen and hydroxy derivatives function equally well for improving the film strength and reducing the oxidation and sludge forming tendencies of lubricating oils.
- Sulfur heterocyclics whose amines are suitable for the preparation of the amide addition agents herein disclosed, include those such as thiophene, benzo thiophene, thiophanthrene, thianthrene, thiopyrylium, thiazole, thioxane, and the like, together with their alkyl, aryl, aryl-alkyl homologues and their hydro-, nitro-, halogen and hydroxy derivatives.
- Acids suitable for acylation include aliphatic acids as acetic, butyric, and the like, aromatic acids as benzoic, toluic, phthalic and the like.
- the acylation may be accomplished by use of the acids directly, their anhydrides or acid halides.
- An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of an acylated derivative of an amino heterocyclic sulfur compound containing the sulfur in the ring and the amino group as a side chain having the general formula XNH- OCR in'which X is aheterocyclic radical containing sulfur in the ring, and R is selected from a group consisting of alkyl, aryl and aryl-alkyl radicals, together with their hydro-, nitro-, halogen and hydroxy derivatives, to improve the properties of the so treated oil.
- An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of aceto thiophenide, to improve the properties of the so treated oil.
- An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of an addition agent selected from a group consisting of the,hydro-, nitro-, halogen and hydroxy derivatives of aceto thiophenide, to improve the properties of the so treated oil.
- An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of aceto thiophenide to increase the film strength of the so treated oil.
- An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of an addition agent selected from a group consisting of the hydro-, nitro-, halogen, and hydroxy derivatives of aceto thiophenide, to increase the film strength of the so treated 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)
- Lubricants (AREA)
Description
Patented Apr. 7, 1942 LUBRICANT Daniel E. Bergen, Phillips, Tex., assignor to Phillips Petroleum Company, a corporation of Delaware No Drawing. Application January 11, 1941,
, Serial No. 374,133
Claims.
amines of sulfur heterocyclic compounds to lubricants to increase the wear resisting properties and to increase the stability of the so treated lubricants towards oxidation and sludge formation.
It is known that certain oiliness or film strengthening agents added to the lubricating oil decrease wear during the starting and operating of cold motors, lower bearing temperature, tend to prevent ring sticking and scoring, and to reduce internal friction in some cases. Many of these film strengthening agents, while having the mentioned beneficial efifects, have deleterious effects such as affecting adversely the corrosiveness, oxygemstability and resistance to sludge formation of the oil.
It is known that heterocyclic sulfur compounds when added to petroleum oils have little or no benefiial effect upon the oils. On the contrary, free .amines of heterocyclic sulfur compounds will decrease the susceptibility of oils to oxidation. However, such amines are usually so unstable toward oxidation and polymerization in themselves as to make their manufacture and use impractical. For example, amino thiophene is oxidized and polymerized to an insoluble solid in a few minutes time by light and oxygen. By converting such amines to amides of organic acids, for example, by acylation, the resulting compounds are then relatively stable, and are effective in improving the oiliness or film strength, resistance to oxidation and sludge formation properties of oils.
An object of this invention is to provide a lubricant having improved properties such as improved oiliness or film strength, a decreased tendency toward corrosiveness, oxidation, and sludge formation.
An object of this invention is to provide a method for increasing the film strength or oiliness as well as reducing the tendency towards corrosiveness, oxidation and sludge formation of lubricating oils.
Other objects and advantages will be apparent to those skilled in the art from a study of the following disclosure.
I have found that the acid amide derivatives of sulfur containing heterocyclic compounds when added to petroleum oils in amounts generally less than 2%, will decrease the susceptibility of such oils to oxidation and sludge formation, as well as increase their film strength or oiliness. Such amides, or more specifically acid amides, may be prepared by acylation with an organic acid, acid anhydride or acid chloride according to known methods. The resulting acid amides are a relatively stable group of compounds and I have found them to be effective in improving the quality of lubricating oils as herein described.
Aceto thiophenide, which is the acetyl derivative of the relatively unstable amino thiophene and acetic acid, is quite stable. This material when added to a lubricating oil materially improves the properties thereof. This improvement in quality of a so treated oil is evidenced by the following example which tabulates results of Stephens consistorneter tests, as follows:
Example I Saybolt Uni- Transition versal vis Percent aceto tliiophcnide additive point temcosity at perature transition temperature F. Szcondr Oil, no additive 300 39.8 Oil+0.025% additive 311 38. 7 0il+0.05% additive 320 32. 9
The shift of 11 F. and 20 F. in the transition point temperature, and the decrease in viscosity at the transition point indicates a considerable increase in film strength, oiliness or lubricating properties.
The Stephens consistometer, previously manufactured by Stephens Consistome'ter Corporation, 332 South Michigan Avenue, Chicago, Illinois, is a device for use in the testing of lubricants. The device consists of two circular metal plates, one of which is rotated at a constant speed, and to the other plate is attached a recording indicator. These two circular plates are immersed in a bath of the lubricant under test, one plate rotated at constant speed and the drag on the second plate indicated by the recorder. The oil being tested is warmed slowly and a the temperature increases the drag on the second plate decreases due to the thinning of the oil until a temperature is reached at which the oil film breaks and seizure occurs. This temperature is recorded as the transition point temperature. It will be observed from the above data that the oil treated with the very small quantities of aceto thiophenide became tenacious and adhered strongly to the metallic surface and withstood appreciably higher temperatures before failure, and it will be understood by those skilled in the art that transition point temperature increases such as these recorded above are very desirable.
In this same example, it will be noted that the Saybolt Universal viscosity of the treated oil decreased from 39.8 seconds at 300 F. to 32.9 seconds at 320 F. Modern automotive engines require thinner or less viscous oils than heretofore,
When aceto thiophenide is added to an unstable light neutral oil which had formed 38 milligrams of sludge per 10 grams of oil in 18 hours in an Indiana oxidation test, only 22 milligrams of sludge formed in this same period of time.
Aceto thiophenide and its hydro-, nitro-, halogen and hydroxy derivatives function equally well for improving the film strength and reducing the oxidation and sludge forming tendencies of lubricating oils. Sulfur heterocyclics whose amines are suitable for the preparation of the amide addition agents herein disclosed, include those such as thiophene, benzo thiophene, thiophanthrene, thianthrene, thiopyrylium, thiazole, thioxane, and the like, together with their alkyl, aryl, aryl-alkyl homologues and their hydro-, nitro-, halogen and hydroxy derivatives. Acids suitable for acylation include aliphatic acids as acetic, butyric, and the like, aromatic acids as benzoic, toluic, phthalic and the like. The acylationmay be accomplished by use of the acids directly, their anhydrides or acid halides.
I do not wish to be restricted by any theories as to the reasons for the beneficial results obtained by using the acylated amines of sulfur heterocyclic compounds in lubricating oil, but only by the limitation of the following claims.
I claim:
1. An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of an acylated derivative of an amino heterocyclic sulfur compound containing the sulfur in the ring and the amino group as a side chain having the general formula XNH- OCR in'which X is aheterocyclic radical containing sulfur in the ring, and R is selected from a group consisting of alkyl, aryl and aryl-alkyl radicals, together with their hydro-, nitro-, halogen and hydroxy derivatives, to improve the properties of the so treated oil.
2. An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of aceto thiophenide, to improve the properties of the so treated oil.
3. An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of an addition agent selected from a group consisting of the,hydro-, nitro-, halogen and hydroxy derivatives of aceto thiophenide, to improve the properties of the so treated oil.
4. An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of aceto thiophenide to increase the film strength of the so treated oil.
5. An improved lubricant comprising a mineral lubricating oil having incorporated therein less than 2 per cent of an addition agent selected from a group consisting of the hydro-, nitro-, halogen, and hydroxy derivatives of aceto thiophenide, to increase the film strength of the so treated oil.
DANIEL E. BERGEN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US374133A US2278762A (en) | 1941-01-11 | 1941-01-11 | Lubricant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US374133A US2278762A (en) | 1941-01-11 | 1941-01-11 | Lubricant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2278762A true US2278762A (en) | 1942-04-07 |
Family
ID=23475446
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US374133A Expired - Lifetime US2278762A (en) | 1941-01-11 | 1941-01-11 | Lubricant |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2278762A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2643971A (en) * | 1950-06-14 | 1953-06-30 | Standard Oil Co | Combination hf treating catalytic cracking process |
| US3200107A (en) * | 1961-06-12 | 1965-08-10 | Lubrizol Corp | Process for preparing acylated amine-cs2 compositions and products |
| US3256185A (en) * | 1961-06-12 | 1966-06-14 | Lubrizol Corp | Lubricant containing acylated aminecarbon disulfide product |
| US9786442B2 (en) | 2007-10-05 | 2017-10-10 | Carver Scientific, Inc. | Energy storage device |
-
1941
- 1941-01-11 US US374133A patent/US2278762A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2643971A (en) * | 1950-06-14 | 1953-06-30 | Standard Oil Co | Combination hf treating catalytic cracking process |
| US3200107A (en) * | 1961-06-12 | 1965-08-10 | Lubrizol Corp | Process for preparing acylated amine-cs2 compositions and products |
| US3256185A (en) * | 1961-06-12 | 1966-06-14 | Lubrizol Corp | Lubricant containing acylated aminecarbon disulfide product |
| US9786442B2 (en) | 2007-10-05 | 2017-10-10 | Carver Scientific, Inc. | Energy storage device |
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