US2198307A - Lubricant - Google Patents
Lubricant Download PDFInfo
- Publication number
- US2198307A US2198307A US177254A US17725437A US2198307A US 2198307 A US2198307 A US 2198307A US 177254 A US177254 A US 177254A US 17725437 A US17725437 A US 17725437A US 2198307 A US2198307 A US 2198307A
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- Prior art keywords
- oil
- cobalt
- ring
- lubricant
- ether
- Prior art date
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- 239000000314 lubricant Substances 0.000 title description 31
- 239000003921 oil Substances 0.000 description 48
- 239000000203 mixture Substances 0.000 description 30
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
- 239000004215 Carbon black (E152) Substances 0.000 description 22
- 229930195733 hydrocarbon Natural products 0.000 description 22
- 229910052751 metal Inorganic materials 0.000 description 21
- 239000002184 metal Substances 0.000 description 21
- 150000003839 salts Chemical class 0.000 description 20
- 239000002253 acid Substances 0.000 description 15
- 230000001050 lubricating effect Effects 0.000 description 14
- 229910017052 cobalt Inorganic materials 0.000 description 13
- 239000010941 cobalt Substances 0.000 description 13
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 13
- 150000002430 hydrocarbons Chemical class 0.000 description 13
- 150000001298 alcohols Chemical class 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 150000002170 ethers Chemical class 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 150000001868 cobalt Chemical class 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000013329 compounding Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000010688 mineral lubricating oil Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- -1 carboxyl hydrogen Chemical compound 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910021385 hard carbon Inorganic materials 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/124—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms containing hydroxy groups; Ethers thereof
-
- 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
- C10N2010/14—Group 7
-
- 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
- C10N2010/16—Groups 8, 9, or 10
Definitions
- This invention has to do in a general way with the art of compounding lubricants and is more particularly related to an improved lubricant which is especially useful in lubricating engines of the compression ignition type.
- Oilsolates hereinabove referred to are manufactured and sold for use in the paint industry as siccatives, and their preparation and properties as such are discussed at length in an article by Bruson and Stein in Industrial and Engineering Chemistry, volume 26, No. 12, pages 1268 to 1271.
- Oilsolates are metal salts or soaps of a particular class of organic acids, and the particular compounds which we have so far demonstrated as being effective to attain our objectives may be broadly classified as polyvalent metal salts of organic ether acids, such acids being of the general type, R-OCnH2n-COOH, in which R, is a hydrocarbon radical having more than 3 carbon atoms and n is a whole number from 1 to 3.
- the particular soaps or salts of this general group which We have employed in compounding Diesel lubricants and which We have used in the method contemplated by this invention, are the cobalt and aluminum salts of ether acids of the general type referred to above, in which R is a, hydrocarbon radical derived from a commercial alcohol having more than 5 carbon atoms, and in which n is 1.
- these other acids are those which may be obtained by the condensation of a commercial alcohol or amixture of commercial alcohols with monochlor 'acetic acid, according to the procedure outlined in Bruson Patent No. 2,044,968.
- the alcohol constituent in the synthesis of the acids used in demonstrating the effectiveness of these materials was a mixture of higher monohydric alcohols obtained as a by-product from the synthetic manufacture of methanol by the catalytic treatment of hydrogen and carbon monoxide. It is to be understood, however, that while the cobalt and aluminum salts of these particular ether acidsv have been used to demonstrate the effectiveness of these Oilsolate materials as additive Del gredients for lubricants of the type contemated herein, the salts of various other ether ids and of various metals other than cobalt 1d aluminum which are effective to produce n-ilar results are also contemplated as being .thin the scope of this invention.
- This engine inrporated in a dynamometer unit, was in all the tests run at a speed or 1000 R. P. M. and is maintained at a jacket temperature of 375
- the total time of operation was arbitrarily mean as 25 hours, and after operating for this :riod, the engine was taken down and the pisn inspected for ring condition. With many bricants it was necessary to stop the run bere the arbitrary period of 25 hours had exred because of premature failure of the test. ich failure, caused by ring sticking, was best ,dicated by a drop in the power output and also r the relative amount of blowby in .the ex zust.
- R. is a mixtureof hydrocarbon radicals erived from commercial alcohol and is preominantly comprised of hydrocarbon groups aving more than 5 carbon atoms.
- These salts may be considered as typical of salts from the ass represented by the general formula,
- Oil used conventionally refined Mid-Continent oil A. P. I. gravity 26.6 at 60 F.; A. S. T. M. color of 4.5; and Saybolt viscosity of 66 seconds at 210 F.
- the ether acid salts contemplated herein may be used in petroleum lubricant stocks from different sources,-and variously refined, to materially reduce that property of the oil which tends to bring about ring sticking.
- the amount of additive ingredient to be used for this purpose may vary with the type of oil used, but for most purposes we consider that a minor proportion, ranging from .1 to 5.0%, will give satisfactory results. Amounts in the neighborhood of 0.5%- 2% are preferred.
- cobalt salts of ether acids as being preferable to accomplish the objects of our invention, it is not our intention to specifically limit the invention to cobalt salts of particular ether acids, but to include salts of equivalent metals and equivalent acids, of the general type known to the trade as Oilsolates," which are effective to inhibit the ring sticking action of petroleum lubricants under conditions of use similar to those encountered in engines of the Diesel type.
- the temperature used is preferably in excess of 200 F., and the heating is continued until a solution or colloidal suspension is obtained. The heating is then stopped and oil is added until the concentration of cobalt Oilsolate in the oil is reduced to about 20%. This liquid may then be filtered to remove any solid impurities, and in making the final blend from this concentrate the oil to which the concentrate is added is preferably heated to about F. and the concentrate added to the oil at this temperature with stirring.
- lubricant compositions formed by compounding Oilsolates with mineral lubricating oil are much more effective in reducing the wear and abrasive ac tion between relatively moving metal surfaces than the lubricant without the Oilsolate added.
- comparative tests on a Diesel engine under severe operating conditions showed much less wear and abrasive action on the pistons and liners when the engine was lubricated with an oil containing cobalt Oilsolate, than occurred when the engine was operated with the same lubricant stock alone.
- the invention in its broader aspect, is an improved lubricant composition and includes within its scope such changes and modifications as fairly come within the spirit of the appended claims.
- a lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith a small amount of a salt of a .polyvalent metal having the general formula,
- R- is a hydrocarbon radical having more than three carbon atoms, 11. is a whole number from 1 to 3, M is a polyvalent metal, and a: is the valence of the metal.
- a lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith a small amount of a salt of a polyvalent metal having the general formula,
- R is a hydrocarbon radical having more than three carbon atoms, n is a whole number from 1 to 3, M is a metal selected from the group consisting of aluminum and cobalt, and :cis the valence of said metal.
- a lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith a small amount of a cobalt salt of an ether acid having the general formula,
- R is a hydrocarbon radical having more than five carbon atoms.
- a lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith from .1 to 5% of a metal salt of an ether acid having the general formula,
- n is a whole number from 1 to 3 and R is a hydrocarbon radical derived from a highe: monohydric alcohol having more than 5 carboz atoms, the metal of said salt replacing the hydro gen of the carboxyl group.
- a lubricating composition comprising hydrocarbon lubricant oil and in admixtur' therewith from .1 to 5% of a cobalt salt of a1 ether acid having the general formula,
- n is a whole number from 1 to 3 and I is a hydrocarbon radical derived from a highe: monohydric alcohol having more than 5 carbol atoms.
- a lubricating composition comprising e hydrocarbon lubricant oil and in admixture therewith a small. amount of a metal salt of a1 ether acid having the general formula,
- n is a whole number from 1 to 3 and ii which R. is a hydrocarbon radical derived fron a higher monohydric alcohol having more thar five carbon atoms, the metal of said salt replacing the hydrogen of the carboxyl group.
- a lubricating composition comprising 2 hydrocarbon lubricant oil and in admixture therewith a small amount of a metal salt of 2 mixture of ether acids, said acids having the general formula,
- n is a whole number from 1 to 3 ant in which R is derived from a mixture of monohydric alcohols, said mixture of alcohols being predominantly comprised of alcohols having more than five carbon atoms, the metal of saie salt replacing the hydrogen of the carboxyl group.
- a lubricating composition comprising 2 hydrocarbon lubricant oil and in admixture therewith a small amount of a cobalt salt of 2 mixture of ether acids, said acids having the general formula,
- n is a whole number from 1 to 3 am in which E is derived from a mixture of monohydric alcohols, said mixture of alcohols being predominantly comprised of alcohols having more than five carbon atoms.
- A. lubricating composition comprising 2 hydrocarbon lubricant oil and in admixture therewith a small amount of aluminum salt 01 a mixture of ether acids, said adds having the general formula,
- R is derived from a mixture of monohydric alcohols, said mixture of alcohols being predominantly comprised of alcohols havin more than five carbon atoms.
- a lubricating composition comprising 2 hydrocarbon lubricant oil and in admixture therewith a small amount of a metal salt of all: organic ether acid in which the carboxyl hydrogen of said acid is replaced with its equivalent weight of metal.
- a lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith a small amount of a cobalt salt of ar organic ether acid.
Description
Patented Ar. 23, l fi iii Gerard A. Hope, Brooklyn, William L. Linton, Eayside, and Malcolm'F. Pratt, New York, N. Y assignors to Socony-Vacuum Oil Company, Incorporated, New York, N. Y., a corporation of New York No Drawing. Application November 30, 1937, Serial No. 177,254
11 Claims.
This invention has to do in a general way with the art of compounding lubricants and is more particularly related to an improved lubricant which is especially useful in lubricating engines of the compression ignition type.
As is well known to those familiar with the art, the usual type of lubricating oil, under certain conditions of use, such as in internal com.- bustion engines of the Diesel type and those spark ignition engines where piston temperatures are abnormally high, tends to form sticky carbonaceous deposits, which over varying periods of use accumulate in the piston ring grooves,
causing the rings to stick and become ineffec- 15 tive. This problem of the piston ring sticking has assumed considerable importance since the advent of high and medium speed Diesel engines. Although little is known as to the actual cause of ring sticking, it is probably both chemical and physical in nature. It is probably chemical in that the oxidation of the oil may produce sticky materials which build up around the ring areas and eventually limit or completely restrict free motion of the rings. The physical action is indicated by the factthat volatility of the oil, as
measured by consumption rates, appears to have a definite influence on ring sticking;
Irrespective of any theory as to the cause of this ring sticking action, it has been discovered that such action may be materially reduced by the addition to the oil of certain selective materials. We are aware of the fact, for example, that certain naphthenic materials have been compounded With mineral lubricating oil and have been used with varying degrees of success either to inhibit the formation of, or to maintain in solution or suspension, those materials which lead to the phenomenon of ring sticking. We have discovered that these naphthenic compounds, however, while effective to a degree at least on certain types of oil, such as conventionally refined coastal oils, have little or no efiect on other oils, such as solvent refined mid-continent oils.
It therefore becomes the primary object of this invention to provide a lubricant composition which contains an additive ingredient that will prevent the ring sticking action which ordinarily attends the use of the base stock, irrespective of the source of the basestock or the manner in which the same has been refined. It is a further object of this invention to provide a method of inhibiting or preventing the formation of sticky and carbonaceous deposits on metal surfaces, such as piston rings and the like, which are in contact with hydrocarbon lubricant oils under pressure and temperature conditions at which such deposits would normally form. With these objects in' mind, we have discovered that so certain metal salts of organic ether acids, which are commercially available to the trade under the trade name of Oilsolates, may be added to mineral lubricants of the type ordinarily used in Diesel engines to provide a lubricant blend which is substantially devoid of those properties that lead to ring sticking.
The Oilsolates hereinabove referred to are manufactured and sold for use in the paint industry as siccatives, and their preparation and properties as such are discussed at length in an article by Bruson and Stein in Industrial and Engineering Chemistry, volume 26, No. 12, pages 1268 to 1271. It will be understood, therefore, that these compositions per se and their method of preparation form no part of the present invention, which is directed to a lubricating composition comprised of a major portion of a hy drocarbon lubricant and a minor proportion of an Oilsolate compound and to a method of inhibiting the formation of ring sticking deposits about the piston rings of an internal combustion engine which comprises providing the surface of the piston and said rings with a film of hydrocarbon lubricant oil containing a small amount of an Oilsolate compound.
As is stated above, the Oilsolates, or the compounds contemplated as additive ingredients herein, are metal salts or soaps of a particular class of organic acids, and the particular compounds which we have so far demonstrated as being effective to attain our objectives may be broadly classified as polyvalent metal salts of organic ether acids, such acids being of the general type, R-OCnH2n-COOH, in which R, is a hydrocarbon radical having more than 3 carbon atoms and n is a whole number from 1 to 3. The particular soaps or salts of this general group, which We have employed in compounding Diesel lubricants and which We have used in the method contemplated by this invention, are the cobalt and aluminum salts of ether acids of the general type referred to above, in which R is a, hydrocarbon radical derived from a commercial alcohol having more than 5 carbon atoms, and in which n is 1. In other words, these other acids are those which may be obtained by the condensation of a commercial alcohol or amixture of commercial alcohols with monochlor 'acetic acid, according to the procedure outlined in Bruson Patent No. 2,044,968. The alcohol constituent in the synthesis of the acids used in demonstrating the effectiveness of these materials was a mixture of higher monohydric alcohols obtained as a by-product from the synthetic manufacture of methanol by the catalytic treatment of hydrogen and carbon monoxide. It is to be understood, however, that while the cobalt and aluminum salts of these particular ether acidsv have been used to demonstrate the effectiveness of these Oilsolate materials as additive Del gredients for lubricants of the type contemated herein, the salts of various other ether ids and of various metals other than cobalt 1d aluminum which are effective to produce n-ilar results are also contemplated as being .thin the scope of this invention. In this re- .rd, reference is made to the Bruson Patent vove referred to and to Bruson Patent No. 320,160 for equivalent ether acids and ether id salts and their methods of preparation. To demonstrate the efiectiveness of the comundscontemplated herein as additive ingredits for Diesel lubricants to inhibit the ring Lcking action referred to, we have employed series of actual operation tests using a single linder Diesel type engine under accelerated ierating conditions, with various lubricating ls and lubricating oil blends to determine the :tent to which ring sticking actually occurs .th these various lubricants. This engine, inrporated in a dynamometer unit, was in all the tests run at a speed or 1000 R. P. M. and is maintained at a jacket temperature of 375 The total time of operation was arbitrarily mean as 25 hours, and after operating for this :riod, the engine was taken down and the pisn inspected for ring condition. With many bricants it was necessary to stop the run bere the arbitrary period of 25 hours had exred because of premature failure of the test. ich failure, caused by ring sticking, was best ,dicated by a drop in the power output and also r the relative amount of blowby in .the ex zust.
As stated above, the particular additive ingre- .ents employed in these tests were the cobalt ad aluminum salts of ether acids or mixed ether :ids having the general formula,
R-O-CHz-COOH,
1 which R. is a mixtureof hydrocarbon radicals erived from commercial alcohol and is preominantly comprised of hydrocarbon groups aving more than 5 carbon atoms. These salts may be considered as typical of salts from the ass represented by the general formula,
alution in the oil. Most of these tests, thereare, were conducted with the cobalt salts.
The following results are indicative of the imrovem'ent that is effected in a Diesel lubricant y the use therein of these ether acid salts, which 1 the table below are referred to by their trade .ame, "ilsolates.
Exnnmn I Oil used -Conventionally refined coastal oil; A. P. I. ravity of 22.3 at 60 F.; A. S. T. M. color of 2; vnd Saybolt viscosity of 60 seconds at 210 F.
Operation The engine with this oil alone operated 13% LOUIS. The removal of the piston was difiicult. .he first three rings were completely stuck, the i1 ring was half stuck and the fourth ring sticky.
with the same oil containing 1.0% cobalt Oilsolate the engine was operating satisfactorily at the end of 26% hours, when the run was stopped. The piston removed easily. The
first ring was only partially stuck and the remaining rings were free. The oil ring was free and clear. f
Exaurnr: H
Oil used conventionally refined Mid-Continent oil, A. P. I. gravity 26.6 at 60 F.; A. S. T. M. color of 4.5; and Saybolt viscosity of 66 seconds at 210 F.
Operation The engine with the oil alone operated 16% hours. The piston removed with difiiculty. All compression rings were stuck. The oil ring was half stuck and the slots were filled with hard carbon.
'With the same oil containing 1% cobalt "Oilsolate the engine operated the full 25-hour period. All of the rings were free and clean with only a trace of deposit in the oil grooves.
Another satisfactory run was made with this same oil containing 0.5% cobalt Oilsolate.
A blend of this oil was also made with 1% aluminum Oilsolate which gave satisfactory operation over the full 25-hour period. All of the rings were free, but, due perhaps to the lesser stability of the aluminum Oilsolate, more sludge was formed in the oil ring slots than with the cobalt Oilsolate.
A. P. I. gravity of 29.3 at 60 F.; A. S. T. M. color.
of 5; and Saybolt viscosity of 6'7 seconds at Operation Using this oil alone the engine operated 6% hours. Two rings were completely stuck, and a third ring was half stuck. Part of the slots in the oil ring were closed.
With the same oil plus 1% cobalt Oilsolate the engine was operated the full period of 25 hours and all of the rings were free and clean.
It will be apparent from the foregoing results thatthe ether acid salts contemplated herein may be used in petroleum lubricant stocks from different sources,-and variously refined, to materially reduce that property of the oil which tends to bring about ring sticking. The amount of additive ingredient to be used for this purpose may vary with the type of oil used, but for most purposes we consider that a minor proportion, ranging from .1 to 5.0%, will give satisfactory results. Amounts in the neighborhood of 0.5%- 2% are preferred. It is to be understood that while we have indicated cobalt salts of ether acids as being preferable to accomplish the objects of our invention, it is not our intention to specifically limit the invention to cobalt salts of particular ether acids, but to include salts of equivalent metals and equivalent acids, of the general type known to the trade as Oilsolates," which are effective to inhibit the ring sticking action of petroleum lubricants under conditions of use similar to those encountered in engines of the Diesel type.
In compounding a lubricating oil with cobalt gether equal parts of the Oilsolate and the oil.
The temperature used is preferably in excess of 200 F., and the heating is continued until a solution or colloidal suspension is obtained. The heating is then stopped and oil is added until the concentration of cobalt Oilsolate in the oil is reduced to about 20%. This liquid may then be filtered to remove any solid impurities, and in making the final blend from this concentrate the oil to which the concentrate is added is preferably heated to about F. and the concentrate added to the oil at this temperature with stirring.
Ii will be understood, of course, that while the foregoing is a preferred procedure which may be followed in blending the Oilsolate compound with the oil, our invention is not necessarily limited to this particular procedure.
In addition to the item of preventing ring sticking noted above as a primary feature of this invention, we have discovered that lubricant compositions formed by compounding Oilsolates with mineral lubricating oil, are much more effective in reducing the wear and abrasive ac tion between relatively moving metal surfaces than the lubricant without the Oilsolate added. For example, comparative tests on a Diesel engine under severe operating conditions showed much less wear and abrasive action on the pistons and liners when the engine was lubricated with an oil containing cobalt Oilsolate, than occurred when the engine was operated with the same lubricant stock alone.
It is to be understood, therefore, that while the prevention of ring sticking is stressed herein as.
a primary feature of our invention, the invention, in its broader aspect, is an improved lubricant composition and includes within its scope such changes and modifications as fairly come within the spirit of the appended claims.
We claim:
1. A lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith a small amount of a salt of a .polyvalent metal having the general formula,
wherein R- is a hydrocarbon radical having more than three carbon atoms, 11. is a whole number from 1 to 3, M is a polyvalent metal, and a: is the valence of the metal.
2. A lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith a small amount of a salt of a polyvalent metal having the general formula,
wherein R is a hydrocarbon radical having more than three carbon atoms, n is a whole number from 1 to 3, M is a metal selected from the group consisting of aluminum and cobalt, and :cis the valence of said metal.
3. A lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith a small amount of a cobalt salt of an ether acid having the general formula,
in which R is a hydrocarbon radical having more than five carbon atoms.
4. A lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith from .1 to 5% of a metal salt of an ether acid having the general formula,
R-OCnH2n-CQOH,
in which n is a whole number from 1 to 3 and R is a hydrocarbon radical derived from a highe: monohydric alcohol having more than 5 carboz atoms, the metal of said salt replacing the hydro gen of the carboxyl group.
5. A lubricating composition comprising hydrocarbon lubricant oil and in admixtur' therewith from .1 to 5% of a cobalt salt of a1 ether acid having the general formula,
in which n is a whole number from 1 to 3 and I is a hydrocarbon radical derived from a highe: monohydric alcohol having more than 5 carbol atoms.
6. A lubricating composition comprising e hydrocarbon lubricant oil and in admixture therewith a small. amount of a metal salt of a1 ether acid having the general formula,
in which n is a whole number from 1 to 3 and ii which R. is a hydrocarbon radical derived fron a higher monohydric alcohol having more thar five carbon atoms, the metal of said salt replacing the hydrogen of the carboxyl group.
7. A lubricating composition comprising 2 hydrocarbon lubricant oil and in admixture therewith a small amount of a metal salt of 2 mixture of ether acids, said acids having the general formula,
in which n is a whole number from 1 to 3 ant in which R is derived from a mixture of monohydric alcohols, said mixture of alcohols being predominantly comprised of alcohols having more than five carbon atoms, the metal of saie salt replacing the hydrogen of the carboxyl group.
8. A lubricating composition comprising 2 hydrocarbon lubricant oil and in admixture therewith a small amount of a cobalt salt of 2 mixture of ether acids, said acids having the general formula,
in which n is a whole number from 1 to 3 am in which E is derived from a mixture of monohydric alcohols, said mixture of alcohols being predominantly comprised of alcohols having more than five carbon atoms.
9. A. lubricating composition comprising 2 hydrocarbon lubricant oil and in admixture therewith a small amount of aluminum salt 01 a mixture of ether acids, said adds having the general formula,
in which R is derived from a mixture of monohydric alcohols, said mixture of alcohols being predominantly comprised of alcohols havin more than five carbon atoms.
10. A lubricating composition comprising 2 hydrocarbon lubricant oil and in admixture therewith a small amount of a metal salt of all: organic ether acid in which the carboxyl hydrogen of said acid is replaced with its equivalent weight of metal.
11. A lubricating composition comprising a hydrocarbon lubricant oil and in admixture therewith a small amount of a cobalt salt of ar organic ether acid.
GERARD A. HOPE.
M L. IMTTON. MALCOLM: F. PRATT.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US177254A US2198307A (en) | 1937-11-30 | 1937-11-30 | Lubricant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US177254A US2198307A (en) | 1937-11-30 | 1937-11-30 | Lubricant |
Publications (1)
Publication Number | Publication Date |
---|---|
US2198307A true US2198307A (en) | 1940-04-23 |
Family
ID=22647853
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US177254A Expired - Lifetime US2198307A (en) | 1937-11-30 | 1937-11-30 | Lubricant |
Country Status (1)
Country | Link |
---|---|
US (1) | US2198307A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2991248A (en) * | 1957-03-20 | 1961-07-04 | Ici Ltd | Foam inhibited hydrocarbon composition |
US3012966A (en) * | 1958-06-24 | 1961-12-12 | Gen Aniline & Film Corp | Petroleum hydrocarbon compositions |
-
1937
- 1937-11-30 US US177254A patent/US2198307A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2991248A (en) * | 1957-03-20 | 1961-07-04 | Ici Ltd | Foam inhibited hydrocarbon composition |
US3012966A (en) * | 1958-06-24 | 1961-12-12 | Gen Aniline & Film Corp | Petroleum hydrocarbon compositions |
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