US2213804A - Lubricating oil - Google Patents

Lubricating oil Download PDF

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US2213804A
US2213804A US191955A US19195538A US2213804A US 2213804 A US2213804 A US 2213804A US 191955 A US191955 A US 191955A US 19195538 A US19195538 A US 19195538A US 2213804 A US2213804 A US 2213804A
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lubricant
sulphur
compounds
oil
hydrocarbon
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US191955A
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Bert H Lincoln
Gordon D Byrkit
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ConocoPhillips Co
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Continental Oil Co
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    • 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
    • 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • 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
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • 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
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/102Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon only in the ring
    • 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
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • 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
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/106Thiadiazoles
    • 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
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • 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
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/06Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
    • 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
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/06Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
    • C10M2223/061Metal salts
    • 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
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/08Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-nitrogen bonds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • Our invention relates to lubricating oils and more particularly to a lubricating oil of high quality containing an addition agent improving its film strength and oiliness.
  • the product of our invention has a very important property oi reacting with the metal surfaces, penetrating or absorbing on the metal surfaces, and leaving a film of lubricant with high oiliness character, which remains on the metal surface irrespective of the length of time the machine has been idle.
  • This high oiliness film gives very even and smooth operation, which may be easily discerned by the experienced operator and lubricating engineer.
  • hydrocarbon lubricants When the hydrocarbon lubricants are diluted with unburned fuel or with other light hydrocarbons the small degree of oiliness of the original hydrocarbon lubricant is greatly decreased.
  • the addition of the products of our invention to hydrocarbon lubricants more than compensates for the loss in olliness and load-carrying ability from dilution.
  • oils and greases change color and/or deteriorate when exposed to light or the oxygen of the air during use or storage.
  • Deterioration during use of a hydrocarbon oil in an internal combustlon engine takes the course of sludge formation and the production of solubleacids and/or corrosive materials.
  • ordinary lubricants are low, in film strength.
  • oxidation inhibitors or antioxidant materials such as weakly basic nitrogen compounds including the aliphatic amines and the like, or metallic compounds including compounds of tin, chromium, zinc and the like, be employed.
  • One object of our invention is to provide a lubricant which has a reduced tendency to orddize and form sludge and soluble oxidation products.
  • Another object of our invention is to provide a lubricant of increasedfilm strength.
  • a further object of our invention is to provide a stabilized lubricant which produces in use less material corrosive to the parts being lubricated.
  • a still further object of our invention is to provide a lubricant which may be used from five to ten times as long as ordinary lubricants before it is necessary to discard the lubricant on account of its corrosive action on the parts being lubricated.
  • our invention comprises the addition of relatively small amounts oi stable, heterocyclic sulphur compounds to hydrocarbon lubricants.
  • the hydrocarbon portion of our compound may be comparatively viscous or nonviscous, refined or unrefined, natural or synthetic.
  • any hydrocarbon oil may be used within the scope of our invention.
  • the sulphur compounds designed to be used as addition agents contain sulphur in a 'very stable form; that is, firmly bound in a chemical combination.
  • none of the compounds included in our invention may be made by direct treatment of any material with sulphur, or sulphur chloride with or without the aid of heat.
  • heterocyclic compounds. of sulphur when added in small quantities to an otherwise finished lubricant, form mixtures having corrosion inhibiting properties, improved film strength and long life.
  • these. compounds inhibit the formation offinely divided oil-insoluble carbonaceous material commonly known as sludge. prevents lubricants to which our compounds have been added from darkening in use or storage.
  • Our invention consists in adding to an otherwise finished lubricant, a suitable amount of a heterocyclie organic compound containing at least one ring consisting of carbon-and other atoms but including in such ring at least two sul- .phur atoms.
  • a heterocyclie organic compound containing at least one ring consisting of carbon-and other atoms but including in such ring at least two sul- .phur atoms.
  • Other atoms beside carbon and sulphur such as oxygen, nitrogen, and other inorganic elements may be present in the ring with the two or more atoms of sulphur or in' other rings or parts .of the molecule.
  • Various substituting groups may be present without impairing the eflectiveness of the two sulphur atom sulphur in those cases in which the correspondrings.
  • groups such as alkyl, aryl, aryl-alkyl, hydroxyl, amino, nitro, carboxyl, cyano, aldehyde, ether carbinol, and others may be pres ent in any part of the molecule.
  • Selenium andtellurium are to be considered equivalents of ing compounds exist.
  • CQHJN O and its derivatives such as thionyl diphenyl pseudo thiocarbazone OtH
  • oil soluble stable sulphur compounds are to be selected.
  • Such compounds as are insoluble in the hydrocarbon oil may be used in colloidal suspension or emulsion in the hydrocarbon oil accompanied by' suitable stabilizing agents for rendering the emulsion or suspension permanent.
  • the selection of a particular compound or combination of compounds to be used as an addition agent to hydrocarbon oil is to be made considering the use to which the blend is put. Thus if water is likely to be present during use, a stable sulphur compound or combination of compounds is selected which are not affected by water. If a particular added stable sulphur compound proves too volatile for its application, a higher boiling stable sulphur compound should be used and the more volatile compound used for blending in a hydrocarbon oil intended for duty at lower temperature.
  • the sludging tendencies may be decreased by as little as 0.01 per cent of some sulphur compounds.
  • the oxidation characteristics of lubricants is very important in some services, and such is improved by sulphur compounds as a rule.
  • the ability to reduce friction is another feature contributed to lubricating oils by some sulphur compounds.
  • a corrosion testing apparatus which comprised an oil container, an electric motor, an electric heater, and a clamp shaft.
  • the oil container comprised an iron cup about four inches in diameter and eight inches deep, equipped with vanes at the sides and bottom thereof.
  • the electric motor was a 9 H. P., operating at 1700 R. P. M: The motor was mounted directly over the oil container.
  • the oil heater was mounted within the oil container and equipped with a temperature control apparatus.
  • the clamping shaft is directly connected to the motor. The other end of the clamping shaft is provided with a bearing in the bottom of the oil container. Adjustable clamps are provided for holding specimen bearings while rotating in the oil container.
  • Test bearings were prepared by sawinggautomobile half bearing inserts into two one-half width pieces.
  • the test bearings were prepared for test by polishing the bearing sur-v faces with number 100 emery paper and weighing. Eight hundred cubic centimeters of the oil to be tested were placed in the cup and agitated by rotating the shaft with half of the bearing clamp attached until the oil reached the testtemperature of 350 F., being raised to this temperature bythe heater. The shaft was then removed and the shaft with test bearings clamped in place and the motor started. Air at a measured rate of 200 cubic centimeters perminute was bubbled through the oil. The motor was stopped at intervals and the test bearings inspected. This process was continued until it was noted that corrosion had commenced.
  • test bearings were then washed with gasoline and then with a solution containing one part toluene, one part ethyl acetate and one part 96 per cent ethyl alcohol. They were then wiped with a soft cloth, dried in an oven and weighed. The weight loss of the test bearings was plotted against the time on cross section paper, showing the time elapsing before corrosion began.
  • a lubricant comprising in combination a hydrocarbon oil and from 0.05 to 2.0 per cent by weight of an organic compound containing at least two sulphur atoms in a heterocyclic ring.
  • a lubricant comprising a major proportion of hydrocarbon oil and from 0.05 to 2.0 per cent of thianthrene.
  • a lubricant comprising a major proportion of hydrocarbon oil and from 0.05 to 2.0 per cent of a substituted thianthrene.
  • a lubricant comprising in combination a hydrocarbon oil and a. small quantity of an organic compound containing at least two nonadj-acent sulfur atoms in a heterocyclic ring.
  • a lubricant comprising in combination a hydrocarbon oil and from 0.05 to 2.0 per cent by weight of an organic compound containing at least two non-adiacent sulfur atoms in a heterocyclic ring.
  • a lubricant comprising in combination a hydrocarbon oil and a small quantity of a cyclic mercaptal.
  • a lubricant comprising in combination a hydrocarbon oil and from 0.05 to 2.0 per cent by weight of a cyclic mercaptal.
  • A'lubricant comprising in combination a hydrocarbon oil and a small quantity of a cyclic mercaptol.
  • a lubricant comprising in combination a hydrocarbon oil and from 0.05 to 2.0 per cent byweight of a cyclic mercaptol.
  • a lubricant comprising in combination a hydrocarbon oil and a small quantity of thianthrene.
  • a lubricant comprising in combination a' 2.0 per

Description

@sterited Sept. 3, w ld Ubliifi TATES Lnanrcsrnyo on.
Bert E. Lincoln and Gordon D. lByrlrit, lonca City, Okla, assignors to Continental Oil Company, lionca'City, Okla, a corporation of Delaware No Drawing. Application February 23, 1938, Serial No. 191,955
16 illaims. (ill. 252-45) Our invention relates to lubricating oils and more particularly to a lubricating oil of high quality containing an addition agent improving its film strength and oiliness.
This application is a continuation in part of our co-pending application, Serial No. 65,090, filed February 21, 1936.
Present-day mechanical devices require lubricating oils of high film strength and of high oiliness characteristics. It has been found that the present-day hydrocarbon lubricants of the very highest quality are deficient in these two very important characteristics. These two properties are of vital importance under conditions of thin film lubrication where the lubricant has been squeezed from between the friction surfaces due to high pressure, slow speeds, and other causes. It is readily seen that the viscosity or the body of the lubricant plays no part in this type of lubrication and that the remaining ruin of 0211 must have a very high film strength and be of high oiliness value to prevent rupture of the him of the lubricant, which would cause seizure, and tend to keep the coeiilcient of friction as low as possible.
Mechanical devices are being designed for higher pressure operation and the film strength of the best quality straight hydrocarbon lubricant has been found to be too low. It will be obvious that an invention which provides the means of improving the film strength of these lubricants is of great importance to the art of lubricant manufacture and to the designer and fabricator of mechanical devices.
Substantially all machines operate in part or at times totally under conditions of boundary or thin film lubrication, under which conditions the oiliness or unctuosity of the lubricant is the first and primary requisite of emcient operation. Those skilled in the art of lubricant manufacture or machine manufacture will readily appreciate the value of an invention that will improve the olliness of these otherwise high quality lubricents.
In starting idle mechanical equipment which is lubricated from a sump by pumping or circulating the lubricant, there is always a short period of time in which the rubbing surfaces must operate under conditions of dry friction if ordinary hydrocarbon lubricants are used. With dry friction, the wear on friction surfaces is extreme; and during cold weather when the lubricant is sluggish or during periods when the lubricating system is not functioning properly for one reason oranother, rubbing surfaces may not only sufier considerable wear but'may be. dam
aged to the point wherethey must be replaced.
The product of our invention has a very important property oi reacting with the metal surfaces, penetrating or absorbing on the metal surfaces, and leaving a film of lubricant with high oiliness character, which remains on the metal surface irrespective of the length of time the machine has been idle.
This high oiliness film gives very even and smooth operation, which may be easily discerned by the experienced operator and lubricating engineer.
When the hydrocarbon lubricants are diluted with unburned fuel or with other light hydrocarbons the small degree of oiliness of the original hydrocarbon lubricant is greatly decreased. We have found that the addition of the products of our invention to hydrocarbon lubricants more than compensates for the loss in olliness and load-carrying ability from dilution.
Most oils and greases change color and/or deteriorate when exposed to light or the oxygen of the air during use or storage. Deterioration during use of a hydrocarbon oil in an internal combustlon engine takes the course of sludge formation and the production of solubleacids and/or corrosive materials. Furthermore, ordinary lubricants are low, in film strength.
In the prior art, it has been suggested that oxidation inhibitors or antioxidant materials such as weakly basic nitrogen compounds including the aliphatic amines and the like, or metallic compounds including compounds of tin, chromium, zinc and the like, be employed.
One object of our invention is to provide a lubricant which has a reduced tendency to orddize and form sludge and soluble oxidation products.
Another object of our invention is to provide a lubricant of increasedfilm strength.
A further object of our invention is to provide a stabilized lubricant which produces in use less material corrosive to the parts being lubricated.
A still further object of our invention is to provide a lubricant which may be used from five to ten times as long as ordinary lubricants before it is necessary to discard the lubricant on account of its corrosive action on the parts being lubricated.
Other and further objects of our invention will appear from the following description.
In general, our invention comprises the addition of relatively small amounts oi stable, heterocyclic sulphur compounds to hydrocarbon lubricants. The hydrocarbon portion of our compound may be comparatively viscous or nonviscous, refined or unrefined, natural or synthetic. In other words, any hydrocarbon oil may be used within the scope of our invention.
In practicing our invention, we use only stable organic sulphur compounds which may contain other inorganic elements, as for example, oxygen, hydrogen, phosphorus, etc. We are aware of the use of sulphur-treated and sulphur-chloride-treated oils in the improvement of lubricating oils. An example of -such sulphur chlorinated oils is shown in U. S. Patent No. 461,513 issued to Sommer, dated bctober 20, 1891. Sulphuretted lard oil and other oils have been used, but all these oils treated with sulphur or, sulphur chloride and the like contain sulphur in a relatively loose, unstable or chemically corrosive condition. In our invention, on the con-' trary, the sulphur compounds designed to be used as addition agents contain sulphur in a 'very stable form; that is, firmly bound in a chemical combination. Furthermore, none of the compounds included in our invention may be made by direct treatment of any material with sulphur, or sulphur chloride with or without the aid of heat.
We have discovered that certain heterocyclic compounds. of sulphur, when added in small quantities to an otherwise finished lubricant, form mixtures having corrosion inhibiting properties, improved film strength and long life. In addition, it has been found that these. compounds inhibit the formation offinely divided oil-insoluble carbonaceous material commonly known as sludge. prevents lubricants to which our compounds have been added from darkening in use or storage.
Furthermore, the addition of our compounds to a lubricant increases its load carrying capacity, thus affording an increased lubricating safety factor in reducing friction and preventing metal to metal contact in bearing and other rubbing surfaces.
Our invention consists in adding to an otherwise finished lubricant, a suitable amount of a heterocyclie organic compound containing at least one ring consisting of carbon-and other atoms but including in such ring at least two sul- .phur atoms. Other atoms beside carbon and sulphur such as oxygen, nitrogen, and other inorganic elements may be present in the ring with the two or more atoms of sulphur or in' other rings or parts .of the molecule. Various substituting groups may be present without impairing the eflectiveness of the two sulphur atom sulphur in those cases in which the correspondrings. Thus, groups such as alkyl, aryl, aryl-alkyl, hydroxyl, amino, nitro, carboxyl, cyano, aldehyde, ether carbinol, and others may be pres ent in any part of the molecule. Selenium andtellurium are to be considered equivalents of ing compounds exist.
Specific examples of compounds which may be used in our invention are:
'Irithioaeetone,
s-c=(on5)l 8C=(OHa)| 1,8,5-trithiane,
trithiobenzals-on-otm This sludge inhibiting property and their derivatives such as thianthrene,
dioctadecyl thianthrene',
S Cn II CuH s and 2,5-diphenyl-L4-dithiine,
CeHr-C=CH BH=CC4H| Examples'of other compounds which may be used are:
l. Dimethylene disulflde,
c fls \B Hz.
and its derivatives, such as:
p s-cm CIHICIHQCOCH=C 8-- Hi- 4. Dithiazolidine,
'om \mm and its derivatives such as phenyl thiuret:
CQHJN=O and its derivatives such as thionyl diphenyl pseudo thiocarbazone OtH|N=N-O='N -s O-rN-CIHI.
a. Dithiodiazole,
and its derivatives such as 2,2-dimethyl-L3- dithiane:
CH:CH:
8. Compounds containing larger than six membered rings with at least two sulphur atoms in the ring such as dithio disalicylide co-s " co-s tetraethenyl hexasulphide:
S S S S cn o -s o om Any of these compounds or other members of the classes represented or their derivatives are CHaCH CHaCH used within the scope of our invention. Preferably we use from .5 to 2 per cent of one or more of these addition agents to lubricating oil; but
in some cases we may use as low as .01 of 1 per cent or as high as 15 per cent or more.
In practicing our invention, oil soluble stable sulphur compounds are to be selected. Such compounds as are insoluble in the hydrocarbon oil may be used in colloidal suspension or emulsion in the hydrocarbon oil accompanied by' suitable stabilizing agents for rendering the emulsion or suspension permanent. The selection of a particular compound or combination of compounds to be used as an addition agent to hydrocarbon oil is to be made considering the use to which the blend is put. Thus if water is likely to be present during use, a stable sulphur compound or combination of compounds is selected which are not affected by water. If a particular added stable sulphur compound proves too volatile for its application, a higher boiling stable sulphur compound should be used and the more volatile compound used for blending in a hydrocarbon oil intended for duty at lower temperature. In general, we prefer to use compounds having boiling points over 150 F. Some of these stable sulphur compounds may be too odoriferous for certainpurposes. In such cases the odor is covered by a suitable perfuming agent. Such details of practice will be apparent to anyone skilled in the art.
It is sometimes advantageous to combine more than one of these compounds in a blend to obtain particular properties. -We accomplish this by mixing two or more of these compounds together and blending the mixture with the hydrocarbon oil or by blending one in the hydrocarbon oil, blending the second into this mixture and so on until the composition is complete.
provement other than film strength to the hydrocarbon 011. For example the sludging tendencies may be decreased by as little as 0.01 per cent of some sulphur compounds. The oxidation characteristics of lubricants is very important in some services, and such is improved by sulphur compounds as a rule. The ability to reduce friction is another feature contributed to lubricating oils by some sulphur compounds.
To test the efiectiveness of these heterocyclic sulphur compounds as corrosion inhibiting agents, we employed a corrosion testing apparatus which comprised an oil container, an electric motor, an electric heater, and a clamp shaft. The oil container comprised an iron cup about four inches in diameter and eight inches deep, equipped with vanes at the sides and bottom thereof. The electric motor was a 9 H. P., operating at 1700 R. P. M: The motor was mounted directly over the oil container. The oil heater was mounted within the oil container and equipped with a temperature control apparatus. The clamping shaft is directly connected to the motor. The other end of the clamping shaft is provided with a bearing in the bottom of the oil container. Adjustable clamps are provided for holding specimen bearings while rotating in the oil container. Test bearings were prepared by sawinggautomobile half bearing inserts into two one-half width pieces. The test bearings were prepared for test by polishing the bearing sur-v faces with number 100 emery paper and weighing. Eight hundred cubic centimeters of the oil to be tested were placed in the cup and agitated by rotating the shaft with half of the bearing clamp attached until the oil reached the testtemperature of 350 F., being raised to this temperature bythe heater. The shaft was then removed and the shaft with test bearings clamped in place and the motor started. Air at a measured rate of 200 cubic centimeters perminute was bubbled through the oil. The motor was stopped at intervals and the test bearings inspected. This process was continued until it was noted that corrosion had commenced. The corroded test bearings were then washed with gasoline and then with a solution containing one part toluene, one part ethyl acetate and one part 96 per cent ethyl alcohol. They were then wiped with a soft cloth, dried in an oven and weighed. The weight loss of the test bearings was plotted against the time on cross section paper, showing the time elapsing before corrosion began.
A number of bearings were tested by this method, with various lubricating oils by themselves and various lubricating oils with various amounts of thianthrene or other heterocyclic sulphur compounds added. The amount of the addition agent added varied between .05 of one per cent and two percent. As a result of these tests, it was found that, if a mineral oil without the addition agent could be run for about four hours before corrosion began, a small amount such as of one per cent of thianthrene could be run for about ten hours before corrosion commenced and that, in general, lubricants to which thianthrene had been added were twice as resistant to corrosion and deterioration as the same lubricants to which no addition agent had been added.
This corrosion resisting and inhibiting effect obtained, too, in hydrocarbon oils which were thickened with various soaps to form greases.
. It will be understood that certain features and The various sulphur compounds may give im-" is within the scope of our claims.
sub-combinations areof utility and may beeinployed without reference to other'features and subcombinations. This is contemplated by and obvious that various changes may be made in details within the scope of our claims without departing'from the spirit of our invention. It is, therefore, to be understood that our invention is not to be limited to the specific details shownand described. I
Having thus described our invention, what we claim is: 1
1. A lubricant vcomprising in combination a hydrocarbon oil and a small quantity of an organic compound containing at least two sulphur atoms in a heterocyclic ring.
2. A lubricant comprising in combination a hydrocarbon oil and from 0.05 to 2.0 per cent by weight of an organic compound containing at least two sulphur atoms in a heterocyclic ring.
3. A lubricant comprising a major proportion of hydrocarbon oil and from 0.05 to 2.0 per cent of thianthrene.
4. A lubricant comprising a major proportion of hydrocarbon oil and from 0.05 to 2.0 per cent of a substituted thianthrene.
5. A lubricant comprising in combination a hydrocarbon oil and a. small quantity of an organic compound containing at least two nonadj-acent sulfur atoms in a heterocyclic ring.
6. A lubricant comprising in combination a hydrocarbon oil and from 0.05 to 2.0 per cent by weight of an organic compound containing at least two non-adiacent sulfur atoms in a heterocyclic ring.
It is further 7. A lubricant comprising in combination a hydrocarbon oil and a small quantity of a cyclic mercaptal.
8. A lubricant comprising in combination a hydrocarbon oil and from 0.05 to 2.0 per cent by weight of a cyclic mercaptal.
9. A'lubricant comprising in combination a hydrocarbon oil and a small quantity of a cyclic mercaptol.
10. A lubricant comprising in combination a hydrocarbon oil and from 0.05 to 2.0 per cent byweight of a cyclic mercaptol.
11. A lubricant comprising in combination a hydrocarbon oil anda small quantity of thianthrene.
12. A lubricant comprising in combination a' 2.0 per
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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2796403A (en) * 1953-11-16 1957-06-18 Texas Co Extreme pressure lubricant compositions
US2796404A (en) * 1953-11-16 1957-06-18 Texas Co Extreme pressure lubricant compositions
US2796402A (en) * 1953-11-16 1957-06-18 Texas Co Extreme pressure lubricant compositions
US3873454A (en) * 1974-03-22 1975-03-25 Mobil Oil Lubricant composition
US3928217A (en) * 1972-10-19 1975-12-23 Erap Lubricating compositions
USB560717I5 (en) * 1971-07-28 1976-02-10
US3966988A (en) * 1971-07-28 1976-06-29 International Flavors & Fragrances Inc. Flavoring compositions and processes utilizing dithiazine compounds
US4031034A (en) * 1974-11-29 1977-06-21 International Flavors & Fragrances Inc. Altering perfume green notes using trithioacetone
WO1992012225A1 (en) * 1991-01-11 1992-07-23 The Lubrizol Corporation Trithianes and phosphorus acid and/or thiophosphorus acid derivatives
US6313075B1 (en) * 1991-08-29 2001-11-06 Leslie R. Rudnick Alkylated thianthrene lubricants

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2796403A (en) * 1953-11-16 1957-06-18 Texas Co Extreme pressure lubricant compositions
US2796404A (en) * 1953-11-16 1957-06-18 Texas Co Extreme pressure lubricant compositions
US2796402A (en) * 1953-11-16 1957-06-18 Texas Co Extreme pressure lubricant compositions
USB560717I5 (en) * 1971-07-28 1976-02-10
US3966988A (en) * 1971-07-28 1976-06-29 International Flavors & Fragrances Inc. Flavoring compositions and processes utilizing dithiazine compounds
US3982034A (en) * 1971-07-28 1976-09-21 International Flavors & Fragrances Inc. Flavoring with 2,4,6-trimethyl-s-trithiane
US3928217A (en) * 1972-10-19 1975-12-23 Erap Lubricating compositions
US3873454A (en) * 1974-03-22 1975-03-25 Mobil Oil Lubricant composition
US4031034A (en) * 1974-11-29 1977-06-21 International Flavors & Fragrances Inc. Altering perfume green notes using trithioacetone
WO1992012225A1 (en) * 1991-01-11 1992-07-23 The Lubrizol Corporation Trithianes and phosphorus acid and/or thiophosphorus acid derivatives
US5824626A (en) * 1991-01-11 1998-10-20 The Lubrizol Corporation Process for preparing trithianes and phosphorus acid and/or thiophosphorus acid derivatives
US6313075B1 (en) * 1991-08-29 2001-11-06 Leslie R. Rudnick Alkylated thianthrene lubricants

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