US2119718A - Lubricating oil - Google Patents
Lubricating oil Download PDFInfo
- Publication number
- US2119718A US2119718A US721971A US72197134A US2119718A US 2119718 A US2119718 A US 2119718A US 721971 A US721971 A US 721971A US 72197134 A US72197134 A US 72197134A US 2119718 A US2119718 A US 2119718A
- Authority
- US
- United States
- Prior art keywords
- lubricating oil
- pour point
- oil
- ester
- glycerol
- 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 23
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 33
- 239000003921 oil Substances 0.000 description 19
- 235000011187 glycerol Nutrition 0.000 description 16
- 150000002148 esters Chemical class 0.000 description 12
- -1 glycerol tri-esters Chemical class 0.000 description 12
- 230000000994 depressogenic effect Effects 0.000 description 10
- 239000001993 wax Substances 0.000 description 9
- 235000021355 Stearic acid Nutrition 0.000 description 8
- 235000021588 free fatty acids Nutrition 0.000 description 8
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 8
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 8
- 239000008117 stearic acid Substances 0.000 description 8
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 8
- 239000010688 mineral lubricating oil Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 150000002314 glycerols Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000010705 motor oil Substances 0.000 description 4
- 150000004671 saturated fatty acids Chemical class 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 239000010685 fatty oil Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 239000013014 purified material Substances 0.000 description 2
- PVNIQBQSYATKKL-UHFFFAOYSA-N tripalmitin Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCC PVNIQBQSYATKKL-UHFFFAOYSA-N 0.000 description 2
- 241000489477 Chlorogalum Species 0.000 description 1
- 235000007836 Chlorogalum pomeridianum Nutrition 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 241000382509 Vania Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic 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
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic 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
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- 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
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated 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
- C10M2207/40—Fatty vegetable or animal oils
-
- 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
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
Definitions
- This invention relates to the manufacture of lubricating oil characterized by a low pour test, and to novel pour point depressants and to methods of producing the same.
- the invention contemplates the preparation of mineral lubricating oil having a reduced pour test and other desired qualities from lubricating oil stock, such as those derived from mixed base and parafiin base crudes and the like, by the addition -.0 to the lubricating oil of a pour point depressant material or wax crystal inhibitor.
- the invention particularly contemplates the addition to a lubrieating oil of glycerol tri-esters of higher saturated fatty acids, such as glycerol tri-stearate.
- the presence of a certain amount of wax in a lubricating oil may be benew ficial from the standpoint of providing a. com paratively fiat temperature-viscosity curve. That is, there is a relatively small change in the viscosity of the oil between temperatures of say 100 F. and 210 F. Consequently, it is of ad- 35 vantage to add to the oil a material which will have the efiect of reducing the pour test or cold test to the'desired extent without the necessity of entirely removing the remaining wax.
- a glycerol tri-ester of a higher saturated fatty acid such-as glycerol tristearate or glycerol tri-palmitate, constitutes a highly effective pour depressant material for purposes of the present invention.
- the ester may be prepared from chemically pure stearic acid and glycerine; or commercial stearic acid, or other relatively impure stearic acid such as that recovered from soap plants, grease plants and the like, may be used.
- the esterification may be carried out in conventional manner, such as that 50 suggested by Bellucci (J. Chem. Soc. 1911, A. i. 416).
- the theoretical amounts of glycerine and fatty acid to form the tri-ester are mixed, and the esterification carried out under high vacuum while gradually heating the reactants to a temperature of about 260 C. and maintaining them at this temperature for about 30 minutes.
- any free fatty acid may be removed by dissolving the reaction product in ether, washing out with dilute caustic soda solution followed by distilled water,
- a purified material consisting essentially of a glycol tri-ester having the properties of the above described synthetic esters may be separated from natural fats or fatty oils, such as oleo-stearin, by a separation and purification treatment, as by repeated pressing at high temperatures, or hydrogenation to reduce the olein content, followed by removal of free fatty acid in the manner outlined above.
- the proportion in which the glycerol ester is added to a lubricating oil is critical in obtaining the desired lowering of pour point with a commercially'practical quantity of the ester.
- increase in the proportion of glycerol ester up to a certain amount for the particular ester, and for a particular wax bearing oil gives increased lowering of pour point; but increase beyond this amount gives no further beneficial eifect, and in fact, may result in raising of the pour point from the low value obtained. with the optimum proportions.
- a proportion of the order of less than 1 g. of the glycerol ester per 100cc. of oil is employed; and as little as g. or less per 100 cc. of oil effects pronounced lowering of the pour point.
- Optimum results with glycerol tri-stearate are secured by the use of approximately to 1% by weight of the depressant.
- natural fats or fatty oils do not possess the pour reducing qualities of the synthetic or purified esters mentioned above, and are commercially ineffective or undesirable for this purpose, particularly in connection with motor oils adapted for crank case lubrication of internal combustion engines.
- the depressants of the present invention are particularly valuable because they are colorless materials which have substantially no effect on the color of the oil, and therefore permit their use in connection with pale oils without lowering of color.
- the depressants are also free from metallic bases or soaps, which are objectionable in lubricating oils adapted for certain purposes such as motor oils.
- the small amount of the glycerol ester required to effect a lowering of pour point of as much as 25 to 35 F. has little effect upon other desirable properties of the lubricating oil, as is evident from the following results obtained by tests on a paraffln base lubricating oil before and after addition of 0.5 g. of glycerol ester, prepared from the commercial grade of stearic acid as outlined above, to 100 cc. of the oil.
- paraflin base lubricating oil refers to an oil of the mixed base or Mid-Continent type as well as an oil of the parafiin base, or Pennsyle vania type, unless the contrary appears from the text. 1 Obviously many modifications and variations of the invention, as hereinbefore set forth, may be made without departing from the spirit and scope thereof, and therefore only such limitations should be imposed as are indicated in the appended claims.
- a lubricating oil having a pour point of approximately 5 F. or below comprising a mixture of a partially dewaxed paraffin base lubricating oil normally having a pour point above 15 F.
- pour point depressant consisting essentially of a glycerol tri-ester of a higher saturated fatty acid in the proportion of from 0.25 g. to 1.50 g. per 100 cc. of oil, the depressant being substantially devoid of free fatty acid.
- a lubricating oil having a pour point of approximately 5 F. or below comprising a mixture of a partially dewaxed paraflin base lubricating oil normally having a pour point above 15 F., with a. pour point depressant consisting essentially of glycerol tri-stearate in the proportion of from 0.25 g. to 1.00 g. per 100 cc. of oil, the depressant being substantially devoid of free fatty acid.
- a lubricating oil having a lowered pour point comprising a mixture of a partially dewaxed paramn base lubricating oil normally having a higher pour point with small proportion 01' the order of to 1 of the glycerol ester prepared by reacting glycerin with commercial stearic acid, the ester being substantially devoid of free fatty acid.
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 June 7, i938 2,119,118 LnaarcA'rING on.
Ernest F. Pevere, Beacon, N. Y., assigncr to The Texas Company, New York, N. Y., a corporation of Delaware No Drawing. Application April 23, 1934, Serial No. 721,971
Claims.
This invention relates to the manufacture of lubricating oil characterized by a low pour test, and to novel pour point depressants and to methods of producing the same.
5 The invention contemplates the preparation of mineral lubricating oil having a reduced pour test and other desired qualities from lubricating oil stock, such as those derived from mixed base and parafiin base crudes and the like, by the addition -.0 to the lubricating oil of a pour point depressant material or wax crystal inhibitor. The invention particularly contemplates the addition to a lubrieating oil of glycerol tri-esters of higher saturated fatty acids, such as glycerol tri-stearate.
l5 Lubricating oil stocks derived from parafin and mixed base crudes. contain appreciable amounts of wax and, therefore, have a relatively high pour test unless a substantial amount of this wax is removed. The removal of this wax is usually an accomplished by cold settling, filtration or centrifuging. However, lubricating oil stoclg, after dewaxing by these processes, may still retain some wax, and may have a pour test above F. and up to about 40 F. The removal of further quan- 25 titles of wax from these stocks in order to further reduce the pour test necessitates exr'" sire further processing.
0n the other hand, the presence of a certain amount of wax in a lubricating oil may be benew ficial from the standpoint of providing a. com paratively fiat temperature-viscosity curve. That is, there is a relatively small change in the viscosity of the oil between temperatures of say 100 F. and 210 F. Consequently, it is of ad- 35 vantage to add to the oil a material which will have the efiect of reducing the pour test or cold test to the'desired extent without the necessity of entirely removing the remaining wax.
I have discovered that a glycerol tri-ester of a higher saturated fatty acid, such-as glycerol tristearate or glycerol tri-palmitate, constitutes a highly effective pour depressant material for purposes of the present invention. The ester may be prepared from chemically pure stearic acid and glycerine; or commercial stearic acid, or other relatively impure stearic acid such as that recovered from soap plants, grease plants and the like, may be used. The esterification may be carried out in conventional manner, such as that 50 suggested by Bellucci (J. Chem. Soc. 1911, A. i. 416). For example, the theoretical amounts of glycerine and fatty acid to form the tri-ester are mixed, and the esterification carried out under high vacuum while gradually heating the reactants to a temperature of about 260 C. and maintaining them at this temperature for about 30 minutes. Following the esterification, any free fatty acid may be removed by dissolving the reaction product in ether, washing out with dilute caustic soda solution followed by distilled water,
(on. sir-9) and then evaporating the ether to obtain the purified synthetic ester. A purified material consisting essentially of a glycol tri-ester having the properties of the above described synthetic esters may be separated from natural fats or fatty oils, such as oleo-stearin, by a separation and purification treatment, as by repeated pressing at high temperatures, or hydrogenation to reduce the olein content, followed by removal of free fatty acid in the manner outlined above.
The proportion in which the glycerol ester is added to a lubricating oil is critical in obtaining the desired lowering of pour point with a commercially'practical quantity of the ester. Thus, it is found that increase in the proportion of glycerol ester up to a certain amount for the particular ester, and for a particular wax bearing oil, gives increased lowering of pour point; but increase beyond this amount gives no further beneficial eifect, and in fact, may result in raising of the pour point from the low value obtained. with the optimum proportions. Ordinarily, a proportion of the order of less than 1 g. of the glycerol ester per 100cc. of oil is employed; and as little as g. or less per 100 cc. of oil effects pronounced lowering of the pour point. Optimum results with glycerol tri-stearate are secured by the use of approximately to 1% by weight of the depressant.
By way of example, the following results were obtained by the addition of the specified amounts of the listed depressants to a partially dewaxed paraffln base lubricating oil having a Saybolt viscosity at 100 F; of 300, and a Saybolt viscosity at 210 F. of 50, with a normal pour point of F.
Pour point in F. of
sample containing designatcd insight ii: Ma'ximum grams 0 epressan Pour point depressant per 100 w f oil 33:3 point, F
it A 3 4 1 Glycerol ester made from '(commerciul) stcaric acid M. P.52.2 G 5 --l0 l5 10 35 Glycerol ester made from grease plant stearic acid M.P.53.30 +5 0 -5 Qlyceroltri-stcarate (LP... -6 25 I am aware that mineral lubricating oils have been blended with natural fats or fatty oils, usually in higher proportions, to produce compounded oils for various uses. My invention, on the other hand, is connected with a function not previously recognized or attained by the above practice. This is the reduction in pour point, and is distinguished by the use of a particular character of partially dewaxed paraflln base lu bricating oil normally having a pour point in excess of 15 F., and by the addition thereto of a very small proportion of a particular synthetic glycerol tri-e'ster of a higher saturated fatty acid, or a purified material consisting essentially of such an ester and having the properties of such a synthetic ester. I have found that natural fats or fatty oils do not possess the pour reducing qualities of the synthetic or purified esters mentioned above, and are commercially ineffective or undesirable for this purpose, particularly in connection with motor oils adapted for crank case lubrication of internal combustion engines.
I am also aware that it has been proposed to add in small proportion to mineral lubricating oils, such as motor oils, an ester selected from a large variety of synthetic organic esters, for the purpose of adding oiliness and increasing the bearing load capacity of the lubricants by reducing friction. My invention is distinguished from this suggestion by relating to the different function of reduction in pour point, which was not recognized or'attained in the former suggestion, due to the use of different mineral lubricating oils of the naphthene base type or fully dewaxed type having initially low pour points, due to the use of a proportion range which lies mainly outside of the effective range of the present invention, and due to the use of a large variety of esters mainly of different classification, and of which substantially all are commercially ineffective for purposes of the present invention.
The depressants of the present invention are particularly valuable because they are colorless materials which have substantially no effect on the color of the oil, and therefore permit their use in connection with pale oils without lowering of color. The depressants are also free from metallic bases or soaps, which are objectionable in lubricating oils adapted for certain purposes such as motor oils. The small amount of the glycerol ester required to effect a lowering of pour point of as much as 25 to 35 F. has little effect upon other desirable properties of the lubricating oil, as is evident from the following results obtained by tests on a paraffln base lubricating oil before and after addition of 0.5 g. of glycerol ester, prepared from the commercial grade of stearic acid as outlined above, to 100 cc. of the oil.
Paraifin base lubricating oil 25.1 A. P. I. 400-405" F. 460-460 F.
Actual service tests of motor oils prepared in accordance with the present invention, in which the oils are used in the crank case of vehicle engines for the usual running period of 1,000 miles or more, indicate that oils ,containing the esters of the present invention in the small proportions disclosed herein, are free from objectionablebearing metal corrosion, sludge formation, or hydrolysis with resultant formation of free fatty acids.
Where the expression paraflin base lubricating oil" is used in the accompanying description and claims, it is to be understood that this refers to an oil of the mixed base or Mid-Continent type as well as an oil of the parafiin base, or Pennsyle vania type, unless the contrary appears from the text. 1 Obviously many modifications and variations of the invention, as hereinbefore set forth, may be made without departing from the spirit and scope thereof, and therefore only such limitations should be imposed as are indicated in the appended claims.
I claim:
1. A lubricating oil having a pour point of approximately 5 F. or below, comprising a mixture of a partially dewaxed paraffin base lubricating oil normally having a pour point above 15 F.,
with a pour point depressant consisting essentially of a glycerol tri-ester of a higher saturated fatty acid in the proportion of from 0.25 g. to 1.50 g. per 100 cc. of oil, the depressant being substantially devoid of free fatty acid.
2. A lubricating oil having a pour point of approximately 5 F. or below, comprising a mixture of a partially dewaxed paraflin base lubricating oil normally having a pour point above 15 F., with a. pour point depressant consisting essentially of glycerol tri-stearate in the proportion of from 0.25 g. to 1.00 g. per 100 cc. of oil, the depressant being substantially devoid of free fatty acid.
3. The method of preparing a lubricating oil of low pour point of approximately F. or below, which comprises reacting glycerine and commercial stearic acid to form essentially glycerol esters of the higher fatty acids present therein, removing free fatty acid from the glycerol esters, and adding the purified glycerol esters in a proportion of from 0.25 g. to 1.50 g. to 100 cc. of a partially dewaxed parafiln base mineral lubricating oil normally having a pour point of above 15 F. I
4.-A lubricating oil having a pour point of approximately 0 F. or below, comprising a mixture of a partially dewaxed parafiin base lubricating oil normally having a pour point above 15' F., with a pour point depressant consisting essentially of glycerol esters prepared from commercial stearic acid in the proportion of from 0.25 g. to 1.00 g. per 100 cc. of oil, the depressant being substantially devoid of free fatty acid.
5. A lubricating oil having a lowered pour point comprising a mixture of a partially dewaxed paramn base lubricating oil normally having a higher pour point with small proportion 01' the order of to 1 of the glycerol ester prepared by reacting glycerin with commercial stearic acid, the ester being substantially devoid of free fatty acid.
ERNEST F. PEVERE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US721971A US2119718A (en) | 1934-04-23 | 1934-04-23 | Lubricating oil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US721971A US2119718A (en) | 1934-04-23 | 1934-04-23 | Lubricating oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2119718A true US2119718A (en) | 1938-06-07 |
Family
ID=24900009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US721971A Expired - Lifetime US2119718A (en) | 1934-04-23 | 1934-04-23 | Lubricating oil |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2119718A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2891089A (en) * | 1955-12-30 | 1959-06-16 | Sun Oil Co | Mixed esters of polyhydric alcohols with naphthenic and lower fatty acids |
| US2984379A (en) * | 1956-07-27 | 1961-05-16 | Csepel Vas Es Femmuvek | Transport of industrial gases on rolling stock |
| US3132008A (en) * | 1960-08-22 | 1964-05-05 | British Petroleum Co | Fuel oil composition having reduced pour point |
| US5641740A (en) * | 1994-06-24 | 1997-06-24 | Witco Corporation | Lubricating oil having lubrication condition responsive activity |
| US6878678B2 (en) * | 2001-09-13 | 2005-04-12 | Tonen General Sekiyu K.K. | Oil composition for automatic transmission |
-
1934
- 1934-04-23 US US721971A patent/US2119718A/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2891089A (en) * | 1955-12-30 | 1959-06-16 | Sun Oil Co | Mixed esters of polyhydric alcohols with naphthenic and lower fatty acids |
| US2984379A (en) * | 1956-07-27 | 1961-05-16 | Csepel Vas Es Femmuvek | Transport of industrial gases on rolling stock |
| US3132008A (en) * | 1960-08-22 | 1964-05-05 | British Petroleum Co | Fuel oil composition having reduced pour point |
| US5641740A (en) * | 1994-06-24 | 1997-06-24 | Witco Corporation | Lubricating oil having lubrication condition responsive activity |
| US6878678B2 (en) * | 2001-09-13 | 2005-04-12 | Tonen General Sekiyu K.K. | Oil composition for automatic transmission |
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