US2213532A - Lubricating composition - Google Patents
Lubricating composition Download PDFInfo
- Publication number
- US2213532A US2213532A US649734A US64973432A US2213532A US 2213532 A US2213532 A US 2213532A US 649734 A US649734 A US 649734A US 64973432 A US64973432 A US 64973432A US 2213532 A US2213532 A US 2213532A
- Authority
- US
- United States
- Prior art keywords
- halogenated
- compounds
- chlorinated
- oil
- lubricating composition
- 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
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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
- C10M2207/40—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
-
- 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/042—Alcohols; Ethers; Aldehydes; Ketones
-
- 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/044—Acids; Salts or esters thereof
-
- 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/06—Perfluorinated 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/024—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of esters, e.g. fats
Definitions
- This invention relates, as indicated, to lubricating compositions and more particularly, to compositions for use in connection with the lubrication of the working parts of internal combus- 5 tion engines, motor vehicles, etc. and it is among the objects of the invention to provide compositions obviating the disadvantages of the usual petroleum oils.
- the film of lubricant As above indicated, is broken down and if it is not entirely destroyed. the metallic bearing surfaces are still affected to some extent, at least by the presence of the lubricating composition. This condition is commonly referred to as thin-film lubrication.
- . cation may be approximately coordinated into a single curve but only 'on plotting coefficient of friction against the product of viscosity and speed divided by the square root of the pressure.
- both bearing surfaces are of steel, seizure or scoring will result almost immediately upon fail- 5 ure of thick-film lubrication when a pure mineral oil'is the sole lubricating composition employed'.
- this invention comprises incorporating certain forms of halogenated carbon compounds with certain types of oil bases. More specifically, the invention comprises incorporating a halogenated carbon compound with a sulphur-treated oil base and incorporating an oxygen-bearing halogenated carbon compound with any suitable oil base.
- sulphur treated oil as employed in this description, is meant any suitable oil base which has been treated with sulphur, for exam- 40 ple, the composition produced by heating sulphur with a fixed oil, such as lard, oil, or fish oil; or to which sulphur has been added, so that a certain amount of sulphur is present in active or loosely combined form. It has been found that a suit- 45 ab1e oil base containing from 0.50% to 2.50% of sulphur in active or loosely combined form is best suited for use in a composition according to the present invention. These percentages are not to be construed, however, as limitations but merely 60 an indication of the range of sulphur in the form defined for optimum results. g
- oxygen containing carbon ring compounds which have been chlorinated and added to a lubricating oil are capable of 66 sults, viz: halogenated or more specifically, chlorinated oxygen-containing substituted benzene compounds such as:
- chlorinated substitutednaphthalenes such as:
- Chlorinated naphthols as well as the aromatic ethers, phenols, acids, the esters and the aldehydes.
- oxygen-bearing organic ring compounds which are preferably employed (that is, phenols, cresols, diphenyl ether, methyl salicylate, p-phenyl-phenol, di-xenyl ether and naphthols) are compounds of the aryl type, that is compounds containing benzoid ring structures.
- halogenation of these specific oxygen-bearing ring compounds the viscosity of the oil base to generally produces compounds 01' the type in whichthe halogen is directly attached to an atom which is a part of such ring structure.
- halogenated aromatic ester is a halogenated alkyl ester of a hydroxy-aromatic acid (i. e. an ester of a hydroxy-aryl carboxylic acid); more specifically a halogenated ester of hydroxy-benzoic acid.
- halogenated hydroxyaromatic compounds are the chlorinated phenols and cresols, and chlorinated p-phenyl phenol.
- the last-named compound may also be described as a halogenated hydroxy diphenyl.
- halogenated oxygen-containing substituted diphenyls as well as he tuted benzenes where two or more phenyl groups are directly linked, may be inclusively.
- halogenated oxygen-containing substituted polyphenyla Since generally the addition of compoundsof the class including the above enumerated reduce which the same are added, if a large percentage of such compounds are added, there will be a tendency to destroy thick-film lubrication because of such reduction in viscosity. Ifan excessive quantity of such compounds are added, all of the lubrication will then be of the thin-film" type and therefore, produce a decided increase in the amount of friction developed.
- Our invention contemplates incorporating with a suitable oil base a total of less than 20% of at least one halogenated oxygen containing carbon ring compound of the enumerated class.
- halogenated com pound to be employed will depend largely upon the halogen content of the particular compound, its physical characteristics and. especially its effect on the viscosity of the oil to which it is added.
- a composition according to our invention comprises a large proportion of a suitable oil base such as mineral oil and concentrations of from one-half to two per cent. of halogenated compounds of the above class containing from 50% to 25%,of chlorine. If the valve structure of the engine is to be lubricated separately from the remainder of the mechanism or by means acting in an auxiliary fashion, the composition for such purposes will preferably contain a larger amount of such halogenated compounds, i. e., from 2 to 10%.
- the limit'of the amount of the halogenated compounds which may be added to an oily base and which will produce improved results depends, as above indicated, upon the reduction in viscosity of the composition caused by the addition of such compounds, Certain of the more viscous compounds, for example, chlorinated di-pfienyl chlorine, may be without causing too great a reduction of viscosity.
- sulphur-treated oil in combination with halogenated compounds, it should be noted that for sufliciently desirable results, the major proportion of the ultimate composition need not consist entirely of sulphurtreated oil, but a suitable oil base such as mineral oil may have added thereto minor quantities or ,proportions of a, sulphur-treated oil and a halogenated compound.
- a lubricating composition including a major proportion of a hydrocarbon oil and a minor proportion of chlorinated phenol.
- a lubricating composition including a major proportion of a hydrocarbon oil and a minor p.0po'rtion of chlorinated cresol.
- composition of matter which includes a lubricating composition having as a primary lubricating constituent the combination of a major proportion of a suitable oil and a minor proportion of "a halogenated phenol.
- a lubricating composition comprising in combination, a major proportion of a suitable oil base and a minofproportion of a halogenated naphthol.
- a lubricating composition comprising the combination of a major proportion of a suitable oil base and a minor proportion of a halogen bearing aromatic hydroxy compound selected from the class consisting of the halogenated phenols;
Description
Patented Sept. 3, 1940 UNITED STATES PATENT OFFICE 2,213,532 LUBRICATING COMPOSITION Delaware No Drawing. Application December 31, 1932, Serial No. 649,734
6 Claims.
This invention relates, as indicated, to lubricating compositions and more particularly, to compositions for use in connection with the lubrication of the working parts of internal combus- 5 tion engines, motor vehicles, etc. and it is among the objects of the invention to provide compositions obviating the disadvantages of the usual petroleum oils.
It has been explained by specialists in this par- 1 ticular field of the art'that a lubricant employed for the purpose of reducing friction between relatively movable metallic parts functions in two ways commonly referred to as thick-film lubrication and thin-film lubrication.
In thick-film lubrication the bearing surfaces are completely. separated by a relatively thick continuous film of the lubricating composition employed. When friction between the moving parts is measured in this case, the results obtained are independent of all factors except pressure, speed and the viscosity of the lubricating composition. A single curve representing all data may be found by plotting the coefficient of friction against a particular function consisting of the product of the viscosity of the lubricating composition and the speed of relative movement of the parts divided by the pressure per unit area of the bearing surface, as long as the value of such function is greater than a definite amount.
0' At this minimum point, reduction of viscosity or.
speed or an increase in the pressure results in a breaking down of the film of lubricant. Although the value of the coefficient of friction is lowest at the point at which the film is about to break down,
the increase in the coefficient for higher viscosity and speed or lower pressure is relatively slight.
The conditions resulting in thick-film" lubrication are, therefore, those which result in low friction.
For pressures sufliciently great or for correspondingly low values of viscosity or speed, the film of lubricant, as above indicated, is broken down and if it is not entirely destroyed. the metallic bearing surfaces are still affected to some extent, at least by the presence of the lubricating composition. This condition is commonly referred to as thin-film lubrication.
When one of the bearing surfaces is a metal such as bronze or babbitt, seizure does not take place at once but the coeflicient of friction increases rapidly to abnormally high values with each slight further increase in pressure or decrease in viscosity or speed. For a given set of bearings-the data obtained for thin-film lubri-.
. cation may be approximately coordinated into a single curve but only 'on plotting coefficient of friction against the product of viscosity and speed divided by the square root of the pressure.
- If both bearing surfaces are of steel, seizure or scoring will result almost immediately upon fail- 5 ure of thick-film lubrication when a pure mineral oil'is the sole lubricating composition employed'.
It is among the objects of our invention to providea lubricating composition which may be em- 10 ployed to reduce the friction between relatively. movable metallic surfaces under pressures and other factors which result in what has been above explained as thick-film lubrication and a com= position which maybe employed for such thin- 15 film lubrication and Without a material increase in the coefficient of friction between the parts over that found during thick-film" lubrication.
Other objects of our invention will appear as the description proceeds.
To the accomplishment of the foregoing and related ends, said invention, then consists of the means hereinafter fully described and particularly pointed out in the claims.
The following description sets forth in detail 25 one approved combination of ingredients embodying our invention, such disclosed means constituting, however, but one of various forms in which the principle of the invention may be used.
Broadly stated, this invention comprises incorporating certain forms of halogenated carbon compounds with certain types of oil bases. More specifically, the invention comprises incorporating a halogenated carbon compound with a sulphur-treated oil base and incorporating an oxygen-bearing halogenated carbon compound with any suitable oil base.
By the term sulphur treated oil' as employed in this description, is meant any suitable oil base which has been treated with sulphur, for exam- 40 ple, the composition produced by heating sulphur with a fixed oil, such as lard, oil, or fish oil; or to which sulphur has been added, so that a certain amount of sulphur is present in active or loosely combined form. It has been found that a suit- 45 ab1e oil base containing from 0.50% to 2.50% of sulphur in active or loosely combined form is best suited for use in a composition according to the present invention. These percentages are not to be construed, however, as limitations but merely 60 an indication of the range of sulphur in the form defined for optimum results. g
We have found that certain oxygen containing carbon ring compounds which have been chlorinated and added to a lubricating oil are capable of 66 sults, viz: halogenated or more specifically, chlorinated oxygen-containing substituted benzene compounds such as:
Chlorinated phenols Chlorinated cresols Chlorinated diphenylether Chlorinated methyl salicylate; halogenated substituted di-phenyl such as:
Chlorinated p-phenyl phenol Chlorinated di-xenyl ether;
chlorinated substitutednaphthalenes such as:
Chlorinated naphthols; as well as the aromatic ethers, phenols, acids, the esters and the aldehydes.
It will be noted that the above enumerated specific examples of oxygen-bearing organic ring compounds which are preferably employed (that is, phenols, cresols, diphenyl ether, methyl salicylate, p-phenyl-phenol, di-xenyl ether and naphthols) are compounds of the aryl type, that is compounds containing benzoid ring structures.
It will be further noted that halogenation of these specific oxygen-bearing ring compounds the viscosity of the oil base to generally produces compounds 01' the type in whichthe halogen is directly attached to an atom which is a part of such ring structure.
It will be noted that the example of a halogenated aromatic ester given above (chlorinated methyl salicylate) is a halogenated alkyl ester of a hydroxy-aromatic acid (i. e. an ester of a hydroxy-aryl carboxylic acid); more specifically a halogenated ester of hydroxy-benzoic acid.
Other examples listed ,above which may be inclusively' described as halogenated hydroxyaromatic compounds are the chlorinated phenols and cresols, and chlorinated p-phenyl phenol. The last-named compound may also be described as a halogenated hydroxy diphenyl.
As a matter of convenience the halogenated oxygen-containing substituted diphenyls, as well as he tuted benzenes where two or more phenyl groups are directly linked, may be inclusively. referred to as halogenated oxygen-containing substituted polyphenyla' Since generally the addition of compoundsof the class including the above enumerated reduce which the same are added, if a large percentage of such compounds are added, there will be a tendency to destroy thick-film lubrication because of such reduction in viscosity. Ifan excessive quantity of such compounds are added, all of the lubrication will then be of the thin-film" type and therefore, produce a decided increase in the amount of friction developed.
Optimum results are obtained by using minimum quantities of these-halogenated compounds so that their beneficial-eflfect in the region 01' thin-film lubrication will not be overshadowed The particular .added in amounts exceeding 10% event, the resultant composition halogenated oxy en-containing substiby their detrimental eflect inthe region of thick-film lubrication.
Our invention contemplates incorporating with a suitable oil base a total of less than 20% of at least one halogenated oxygen containing carbon ring compound of the enumerated class.
The optimum amount of the halogenated com pound to be employed will depend largely upon the halogen content of the particular compound, its physical characteristics and. especially its effect on the viscosity of the oil to which it is added.
use for which the lubricant is intended is also a governing factor in determining the amount of the compound to be added.
For the purpose of lubricating and reducing the friction between the relatively movable parts 01' an internal combustion engine such as crank case bearings, piston and cylinder surfaces, as
well as piston rings and valves, a composition according to our invention comprises a large proportion of a suitable oil base such as mineral oil and concentrations of from one-half to two per cent. of halogenated compounds of the above class containing from 50% to 25%,of chlorine. If the valve structure of the engine is to be lubricated separately from the remainder of the mechanism or by means acting in an auxiliary fashion, the composition for such purposes will preferably contain a larger amount of such halogenated compounds, i. e., from 2 to 10%.
The limit'of the amount of the halogenated compounds which may be added to an oily base and which will produce improved results depends, as above indicated, upon the reduction in viscosity of the composition caused by the addition of such compounds, Certain of the more viscous compounds, for example, chlorinated di-pfienyl chlorine, may be without causing too great a reduction of viscosity. In any will have inoxide' containing about 50% ferior lubricating properties if the loss of viscosity-is too great as will result from the use of more than 20% of halogenated compounds of ny type- It has been found that for optimum results a tween the amount of chlorine and the amount (if-sulphur, when the halogenated compounds of th above class are added to a sulphur treated oil. It has been found that to anoil base having a low content of sulphur in active or loosely combined form, halogenated compounds should be added in correspondingly low concentrations for best results.
When the halogenated compounds of the above class added to the oil base, are of the closed ring type in contradistinction to the open chain type,
certain advantages are obtained which may be briefly explained as follows:
In case of oil in actual use in machinery of any kind and particularly in the crank case of internal combustion engines, moisture is always present to some extent and due to condensation may even accumulate to form a separate layer. There is always suflicient'water present, therefore, for hydrolysis to take place, particularly when the addition of a chlorinated compound is made to the extent of only a few per cent. 7
Experiments have shown that when compounds which readily hydrolize, such as chlorinatedopen chain compounds, are added to the oily base, hydrolysis will take place to such an extent that the metal parts of any machine being lubricated will be seriously attacked and corroded by the I certain relationship should be maintained be acid generated. On the other hand, the addition of chlorinated carbon ring compounds of the above enumerated class does not cause corrosion.
The composition comprising our invention has certain advantages when used as a lubricant of which the following may be mentioned:
First: By the use of this composition it is possible to extend the pressure range between the bearing surfaces because of the reduced tendency for bearing surfaces so lubricated to Become scored or to seize at higher pressures than are allowable with ordinary lubricants.
Second: The friction between the bearing surfaces is reduced, especially in the higher pressure range below that obtained with ordinary lubricants.
With regard to the use of sulphur-treated oil in combination with halogenated compounds, it should be noted that for sufliciently desirable results, the major proportion of the ultimate composition need not consist entirely of sulphurtreated oil, but a suitable oil base such as mineral oil may have added thereto minor quantities or ,proportions of a, sulphur-treated oil and a halogenated compound.
Certain subject matter disclosed but not- 2. A lubricating composition including a major proportion of a hydrocarbon oil and a minor proportion of chlorinated phenol.
3. A lubricating composition including a major proportion of a hydrocarbon oil and a minor p.0po'rtion of chlorinated cresol.
4. A composition of matter which includes a lubricating composition having as a primary lubricating constituent the combination of a major proportion of a suitable oil and a minor proportion of "a halogenated phenol.
5. A lubricating composition comprising in combination, a major proportion of a suitable oil base and a minofproportion of a halogenated naphthol.
6. A lubricating composition comprising the combination of a major proportion of a suitable oil base and a minor proportion of a halogen bearing aromatic hydroxy compound selected from the class consisting of the halogenated phenols;
CARL F. PRUTTON. ALBERT K..SMITH.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US649734A US2213532A (en) | 1932-12-31 | 1932-12-31 | Lubricating composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US649734A US2213532A (en) | 1932-12-31 | 1932-12-31 | Lubricating composition |
Publications (1)
Publication Number | Publication Date |
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US2213532A true US2213532A (en) | 1940-09-03 |
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ID=24606007
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US649734A Expired - Lifetime US2213532A (en) | 1932-12-31 | 1932-12-31 | Lubricating composition |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3226325A (en) * | 1963-04-30 | 1965-12-28 | Monsanto Res Corp | Lubricant composition containing a halophenol |
-
1932
- 1932-12-31 US US649734A patent/US2213532A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3226325A (en) * | 1963-04-30 | 1965-12-28 | Monsanto Res Corp | Lubricant composition containing a halophenol |
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