US2213532A - Lubricating composition - Google Patents

Lubricating composition Download PDF

Info

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
Application number
US649734A
Inventor
Carl F Prutton
Albert K Smith
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lubrizol Development Corp
Original Assignee
Lubrizol Development Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Lubrizol Development Corp filed Critical Lubrizol Development Corp
Priority to US649734A priority Critical patent/US2213532A/en
Application granted granted Critical
Publication of US2213532A publication Critical patent/US2213532A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/404Fatty vegetable or animal oils obtained from genetically modified species
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/04Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
    • C10M2211/042Alcohols; Ethers; Aldehydes; Ketones
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/04Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
    • C10M2211/044Acids; Salts or esters thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/02Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
    • C10M2219/024Sulfur-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.
US649734A 1932-12-31 1932-12-31 Lubricating composition Expired - Lifetime US2213532A (en)

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
US2213532A true US2213532A (en) 1940-09-03

Family

ID=24606007

Family Applications (1)

Application Number Title Priority Date Filing Date
US649734A Expired - Lifetime US2213532A (en) 1932-12-31 1932-12-31 Lubricating composition

Country Status (1)

Country Link
US (1) US2213532A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226325A (en) * 1963-04-30 1965-12-28 Monsanto Res Corp Lubricant composition containing a halophenol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226325A (en) * 1963-04-30 1965-12-28 Monsanto Res Corp Lubricant composition containing a halophenol

Similar Documents

Publication Publication Date Title
US2285853A (en) Lubrication
US2129281A (en) Lubricating oils
US2158096A (en) Lubricant
US2370299A (en) Compounded lubricant
US2370300A (en) Lubricant
US2261888A (en) Steam turbine lubrication
US2213532A (en) Lubricating composition
US2372411A (en) Compounded lubricating oil
US2432095A (en) Lubricating composition
US2204620A (en) Lubricating composition
US2262773A (en) Lubrication
CA2090647A1 (en) Lubricating oil compositions for internal combustion engines having silver bearing parts
US1986645A (en) Method of lubricating and reducing friction
US2137784A (en) Lubricant and method of lubricating
US2291442A (en) Upper cylinder lubricant
US2387999A (en) Lubrication
US2347217A (en) Lubricating composition
US2250384A (en) Lubricant
US2330238A (en) Lubricating composition
US2243420A (en) Lubricating composition
US2289509A (en) Lubricant
US2068635A (en) Engine fuel
US2322209A (en) Lubricating composition
US2051744A (en) Lubricating composition and method of lubricating and improving the lubricating properties of oils
US2180008A (en) Lubricating oil