US2260625A - Gel and lubricant made therefrom - Google Patents

Gel and lubricant made therefrom Download PDF

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Publication number
US2260625A
US2260625A US184843A US18484338A US2260625A US 2260625 A US2260625 A US 2260625A US 184843 A US184843 A US 184843A US 18484338 A US18484338 A US 18484338A US 2260625 A US2260625 A US 2260625A
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Prior art keywords
gel
oil
aerogel
liquid
oils
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US184843A
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Samuel S Kistler
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Monsanto Chemicals Ltd
Monsanto Chemical Co
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Monsanto Chemicals Ltd
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Priority claimed from US151969A external-priority patent/US2188007A/en
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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
    • C10M5/00Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/0091Preparation of aerogels, e.g. xerogels
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/06Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/08Silica
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00Silicon; Compounds thereof
    • C01B33/113Silicon oxides; Hydrates thereof
    • C01B33/12Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C01B33/14Colloidal silica, e.g. dispersions, gels, sols
    • C01B33/157After-treatment of gels
    • C01B33/158Purification; Drying; Dehydrating
    • C01B33/1585Dehydration into aerogels
    • 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
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
    • 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
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
    • C10M2201/042Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
    • 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
    • C10M2201/04Elements
    • C10M2201/043Sulfur; Selenenium; Tellurium
    • 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
    • C10M2201/06Metal compounds
    • C10M2201/062Oxides; Hydroxides; Carbonates or bicarbonates
    • 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
    • C10M2201/06Metal compounds
    • C10M2201/063Peroxides
    • 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
    • C10M2201/10Compounds containing silicon
    • C10M2201/102Silicates
    • 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
    • C10M2201/10Compounds containing silicon
    • C10M2201/105Silica
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/026Butene
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/12Polysaccharides, e.g. cellulose, biopolymers
    • 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
    • C10M2211/02Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/20Containing nitrogen-to-oxygen 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
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/044Polyamides
    • 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
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/045Polyureas; Polyurethanes
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • 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

  • This invention pertains to the art of thickening liquids and more particularly it relates to a lubricating oil of increased viscosity and the method of preparing the same.
  • Oils have heretofore been thickened or rendered more viscous by admixture withother materials, but it-has been necessary that the matter introduced be added in relatively large amounts to achieve the desired result.
  • a further object of this invention is the provision of a thickened oil which shows an abnormally small change in viscosity with variations in temperature.
  • This invention also contemplates the provision of an addition agent for oils and similar liquids which under conditions of use is inert to the liquid and the bearings or other parts with which the liquid comes in contact during normal usage.
  • the invention contemplates a thickening agent which is unaffected by operating temperatures, and lubricating oils and greases embodying such thickening agents which possess markedly improved properties when compared to present day lubricating oils and greases.
  • My invention further contemplates the provision of a lubricating grease having novel and useful properties as to viscosity; appearance, viscosity index, and stability.
  • This invention includes the discovery that if liquids are thickened with particles of a gel in which the original gel structure is retained substantially intact, the product possesses improved characteristics of great value.
  • compositions of the type to which this invention is directed may be prepared by the addition to the liquid to be thickened of the aerogels described and claimed in U. S. Patent Number 2,093,454 to S. S. Kistler, Similar results are obtainable by replacing the swelling liquid of the gel with a portion of the liquid to be thickened.
  • phase is an organic liquid, as an oil of mineral, animal, or vegetable origin.
  • Inorganic fillers for lubricating oils have been heretofore used for the purpose of thickening the same, and as representativeof this type of addition agent, reference is had to graphite, mica, sulfur, talc, asbestos, and diatomaceous earth. These compounds are reduced to a fine state of subdivision only with some difliculty and the porosity thereof is small. The characteristics of the present compounded oils are attributed in large measure to the high percentage of voids in the thickening agent. It is believed that a comparison of the compositions with those prepared from .diatomaceous earth will point out "most clearly, the advantages of this invention. For the purpose of this comparison tests were made of oils containing silica aerogels.
  • the gels used in these tests were manufactured from hydro-gels of silica made by precipitating silica by addition of sulfuric acid to sodium silicate solution in the well-known manner and washing the gel relatively free of salts with water.
  • This composition is now used in industry as an intermediate in the making of silica gel.
  • the prior practice has been to dry out the gel in any. convenient manner thereby materially reducing the volume of the gel. Such shrinkage is probably due to the force exerted on the solid phase of the gel by the surface tension of the liquid as it recedes in the pores of thematerial. These materials will be referred to as xerogels.
  • the aerogels are composed of the original solid phase of the gel in substantially the same condition as it exists while filled with the swelling liquid. Aerogels are conveniently made by raising the gel to the critical temperature of the liquid con tained therein, while maintaining the pressure on the system sufliciently high to insure that the liquid phase will remain liquid until the critical temperature is reached. At this point, the liquid will'be converted into the gaseous state without the formation of menisci at a gas-liquid interface.
  • the degree of porosity may be controlled to a. large degree by controlling the concentration 56 of silica in the gel as precipitated.
  • the liquid is removed by heating in an autoclave. It is the practice to remove the product by a suction line.
  • the gel is drawn through the centrifugal fan employed to create the suction and during its passage through the fan is reduced to small particles. About 70% of the mass will pass a 100 mesh screen; remains on a 60 mesh screen. It will be understood that when unground aerogel is hereafter referred to, the product referred to is that collected after passage through the fan without further subdivision.
  • a thickened oil is prepared by mixing the thin 01] with a small proportion of aerogel with vigorous mechanical agitation. In order to inhibit settling of the thickening agent, it has been found advisable to grind the mixture in a ball mill for a period depending upon the properties desired, the properties of the oil, and the fineness of the aerogel.
  • the following data is illustrative of results obtained by thickening oils with silica aerogel:
  • the ground gels were ground for the periods indicated in a stone ball mill and the percentages are based on weight.
  • the desired result may also be achieved by forming a greasein the manner of any of the processes described below and adding more oil to the composition by grinding in a ball mill.
  • oils prepared in accordance with the present invention are their relative stability to temperature change.
  • the following table demonstrates this fact by comparison of aerogel containlng oils and untreated oils of comparable viscosity.
  • oil A is a pure SAE No. 20v
  • Oil B is SAE No. 10 oil containing 3% by weight of silica aerogel ground in a ball mill for 24 hours. 40 oil, while oil D is a No. 10 oil containing7% by weight of silica aerogel ground for-24 hours.
  • Oil C is a pure SAE No.
  • a grease of good properties was formedby adding 39 grams of unground aerogel to 350 grams of No. 10 motor oil with vigorous mechanical stirring and subsequently running the resultant slurry through a roller mill several times.
  • the millv used was of the type commonly used togrind paints- It consists of three steel rolls revolving at different speeds. The first and third rolls revolve in the same direction and opposite tov the direction of rotation of the second roll;- the rolls revolve progressively faster in the directionof, the fiowof the material.
  • the shearing action of the rollers serves to grind the oil into the pores of the aerogel, whichv becomes visibly stiffer after the first passage-.throughthe mill and at the end of the sixth pass is found to be a still, transparent, even bodied grease.
  • Such grease is stiff and dry and does not exude oil upon standing for. prolonged periods.
  • Thislatter composition is composed of the original gel structure, with the continuous phase being a petroleum fraction. It is to be understood that gels containing lubricating fluids other than those derived from mineral oil may also be formed, and the following discussion of petrogels is merely illustrative of this feature of the invention.
  • the liquid continuous phase in a gel may be replaced by another liquid, provided the two liquids are mutually miscible.
  • a gel may be prepared in which the continuous phase is a lubricating liquid such as a mineral, vegetable, or animal oil.
  • a lubricating liquid such as a mineral, vegetable, or animal oil.
  • Exemplary of such gels is the result of replacing the water in a silica gel with acetone, replacing the acetone with textile spirits, and then substituting a petroleum lubricating oil for the textile spirits. Such replacements are accomplished by extraction of the gel with the replacing liquid.
  • the petroleum oil is a No. lubricant, a grease having desired properties can then be obtained by the incorporation of additional oil on the roller mill.
  • a lubricant containing the structure of an organic gel such as a swelled resin
  • an organic gel such as a swelled resin
  • a sheet of cellulose (Cellophane) was swelled in sodium hydroxide solution, after which the sodium hydroxide was removed by washing with water and the water in turn was displaced by alcohol.
  • the alcohol was then displaced by ether in orderto obtain a liquid phase that is miscible with an oil of mineral or vegetable origin.
  • the ether gel was thereupon washed with a light petroleum lubricating oil whereby the ether was displaced and there resulted a material in sheet form that is suitable for some types of bearings, and packing for bearings, shafts, etc. since it is essentially a relatively firm sheet of soft material consisting predominately of lubricant.
  • a petro-gel may be formed by immersing in a desired oil, a textile spirits gel,
  • silica gel in which the continuous phase is textile spirits
  • distilling off the textile spirits by any suitable method is the preferred method contemplated by this invention.
  • the preferred method contemplated by this invention is the preparation of a slurry or suspension of textile spirits gel in lubricating oil from which the lighter oil is removed by heating the mixture above the boiling point thereof with agitation. It is to be understood that the invention is not restricted to the use of textile spirits, but rather that any liquid boiling at a temperature substantially below the boiling point of the lubricant may be suitable if miscible with the liquid of the previous step and also with the lubricant.
  • a petro-gel may be made in various ways other than by an intimate mixing or grinding of an aerogel in a ball mill or,a colloid mill with the petroleum oil, or fraction.
  • One method which has been already indicated consists in displacing the water in a hydro-gel such as a silica hydrogel with alcohol and thereafter displacing the alcohol with a liquid which is miscible with the petroleum fraction as, for example, ether, acetone and the like.
  • the general procedure used is described in my co-pending application, Serial No. 151,969, filed July 3, 1937, and my Patent No.
  • the resulting acetone gel or ether gel is mixed with a petroleum cut to give the petrogel.
  • the low-boiling liquid may thereafter, if desired, be removedas by distillation as described.
  • the lubricants and greases of the present invention may include the present day compounding agents used in this art such as the water-soluble soaps, graphite, fats, and material for improving the oiliness characteristics such as chlorinated hydrocarbons of high boiling point; materials which improve the viscosity index characteristics such as polymerized oleflns of high molecular weight, such as Paratone; corrosion inhibitors: chemical stabilizing agents; pigments and the like may be added to the lubricant within the contemplation of the present invention.
  • the present day compounding agents used in this art such as the water-soluble soaps, graphite, fats, and material for improving the oiliness characteristics such as chlorinated hydrocarbons of high boiling point; materials which improve the viscosity index characteristics such as polymerized oleflns of high molecular weight, such as Paratone; corrosion inhibitors: chemical stabilizing agents; pigments and the like may be added to the lubricant within the contemplation of the present invention.
  • lubricants of petroleum origin one may substitute wholly or in part vegetable or animal oils as well as synthetic oils such as those obtained by alkylating aromatic hydrocarbons as is well understood by those skilled in the art.
  • This invention provides a means of thickening oils and forming greases by incorporation therein of a previously formed gel in substantially the form of the gel as originally prepared. By this means it is possible to use relatively small proportions of thickening agent.
  • a further important advantage lies in the provision of a means to incorporate into the liquid 9. thickening agent of high melting point, in order that the effect of the thickening agent will be retained over a much wider range of temperatures than is possible with thickening agents now used in the preparation of of greases.
  • a lubricant comprising an oily liquid substance and a solid substance consisting principally of an inorganic gel formed apart from the liquid substance but'retaining in the thickened liquid the gel structure substantially as formed,
  • said gel being substantially free from liquids other than said oily liquid substance.
  • a lubricating composition comprising an oily liquid substance and a proportion less than 50% by weight of a substantially water free gel originally formed apart from the said composition in an aqueous medium and characterized by the fact that the structure of the water free gel is substantially that of the gel as originally formed.
  • a water immiscible organic oil selected from the group consisting of petroleum hydrocarbons, animal and vegetable oils.
  • a thickened lubricant comprising an oily liquid substance and a solid substance consisting principally of a substantially water free gel originally formed apart i'rom the liquid substance in an aqueous medium, said gel retaining in the thickened liquid substance the gel structure substantially as originally formed.
  • a thickened lubricant comprising an oily liquid substance and a solid substance consisting principally of a substantially water tree .organic gel originally formed apart from the liquid substance in an aqueous medium, said gel retaining in the thickened liquid substance the gel structure substantially as originally formed.
  • a lubricant containing an oily liquid substance and an organic aerogel in an intimate mixture therewith in an amount sumcient to thicken or increase the viscosity of said oily liquid substance, said lubricant being substantially tree of water.
  • a lubricant containing an oily liquid substance and from 10 to 49% by weight or an aerogel based on the weight 01' the mixture, said aerogel being present in an amount sumcient to thicken or increase the viscosity of said liquid substance and form a grease therefrom, and said lubricant being substantially tree of water.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Analytical Chemistry (AREA)
  • Lubricants (AREA)

Description

gels in which the continuous Patented Oct. 28, 1941 GEL AND LUBRICANT MADE THERE-FROM Samuel S. Kistler, West Boylston, Mara, assignor to Monsanto Chemical Company, St. Louis. Mo., a corporation of Delaware No Drawing. Application January 13, 1938,
Serial No. 184,843
Claims.
This invention pertains to the art of thickening liquids and more particularly it relates to a lubricating oil of increased viscosity and the method of preparing the same.
Oils have heretofore been thickened or rendered more viscous by admixture withother materials, but it-has been necessary that the matter introduced be added in relatively large amounts to achieve the desired result. a
It is an object of this invention to provide a thickening agent for oils and other liquids which will materially increase the viscosity of the liquid when the amount of added material is small.
A further object of this invention is the provision of a thickened oil which shows an abnormally small change in viscosity with variations in temperature.
This invention also contemplates the provision of an addition agent for oils and similar liquids which under conditions of use is inert to the liquid and the bearings or other parts with which the liquid comes in contact during normal usage.
As an additional object the invention contemplates a thickening agent which is unaffected by operating temperatures, and lubricating oils and greases embodying such thickening agents which possess markedly improved properties when compared to present day lubricating oils and greases.
My invention further contemplates the provision of a lubricating grease having novel and useful properties as to viscosity; appearance, viscosity index, and stability.
This invention includes the discovery that if liquids are thickened with particles of a gel in which the original gel structure is retained substantially intact, the product possesses improved characteristics of great value.
Compositions of the type to which this invention is directed may be prepared by the addition to the liquid to be thickened of the aerogels described and claimed in U. S. Patent Number 2,093,454 to S. S. Kistler, Similar results are obtainable by replacing the swelling liquid of the gel with a portion of the liquid to be thickened.
In my copending application Serial Number 151,969, there is disclosed a process of preparing phase is an organic liquid, as an oil of mineral, animal, or vegetable origin.
As illustrative of the processes and products forming part of this invention, the preparation of a lubricating oil having incorporated therein a gel will be discussed. In oils intended primarily for lubrication, it is preferred to use gels of substances having a relatively high melting point,
and in that group better results are obtained by use of gels of an inorganic nature. It is to be understood, however, that the principal advantages of my invention can be obtained with aerogels of any material not incompatible with the fluid to be thickened, and the invention contemplates the use of aerogels of silica, magnesia, alumina, gel-forming metal oxides and hydroxides in general, gelatine, albumin, cellulose, and gels of like nature.
Inorganic fillers for lubricating oils have been heretofore used for the purpose of thickening the same, and as representativeof this type of addition agent, reference is had to graphite, mica, sulfur, talc, asbestos, and diatomaceous earth. These compounds are reduced to a fine state of subdivision only with some difliculty and the porosity thereof is small. The characteristics of the present compounded oils are attributed in large measure to the high percentage of voids in the thickening agent. It is believed that a comparison of the compositions with those prepared from .diatomaceous earth will point out "most clearly, the advantages of this invention. For the purpose of this comparison tests were made of oils containing silica aerogels.
The gels used in these tests were manufactured from hydro-gels of silica made by precipitating silica by addition of sulfuric acid to sodium silicate solution in the well-known manner and washing the gel relatively free of salts with water. This composition is now used in industry as an intermediate in the making of silica gel. The prior practice has been to dry out the gel in any. convenient manner thereby materially reducing the volume of the gel. Such shrinkage is probably due to the force exerted on the solid phase of the gel by the surface tension of the liquid as it recedes in the pores of thematerial. These materials will be referred to as xerogels.
As distinguished from the xerogels. the aerogels are composed of the original solid phase of the gel in substantially the same condition as it exists while filled with the swelling liquid. Aerogels are conveniently made by raising the gel to the critical temperature of the liquid con tained therein, while maintaining the pressure on the system sufliciently high to insure that the liquid phase will remain liquid until the critical temperature is reached. At this point, the liquid will'be converted into the gaseous state without the formation of menisci at a gas-liquid interface. The degree of porosity may be controlled to a. large degree by controlling the concentration 56 of silica in the gel as precipitated.
In the method of preparing the aerogel now in use, the liquid is removed by heating in an autoclave. It is the practice to remove the product by a suction line. The gel is drawn through the centrifugal fan employed to create the suction and during its passage through the fan is reduced to small particles. About 70% of the mass will pass a 100 mesh screen; remains on a 60 mesh screen. It will be understood that when unground aerogel is hereafter referred to, the product referred to is that collected after passage through the fan without further subdivision.
A thickened oil is prepared by mixing the thin 01] with a small proportion of aerogel with vigorous mechanical agitation. In order to inhibit settling of the thickening agent, it has been found advisable to grind the mixture in a ball mill for a period depending upon the properties desired, the properties of the oil, and the fineness of the aerogel. The following data is illustrative of results obtained by thickening oils with silica aerogel:
Viseosit Material tested at SAE No. 10 motor oil ll BAE No. 20 motor oil 24 SAE No. 40 motor oil 54 SAE No. 10 oil plus 2'7 unground aerogel... 123 SAE No. 10 oil plus 2% serogel ground 1 hr... 54 BAE No. 10 oil plus 4 a aerogel ground 18 hrs 53 The viscosity measurements were taken on a MacMichael viscosimeter with a No. 26 wire.
The ground gels were ground for the periods indicated in a stone ball mill and the percentages are based on weight. The desired result may also be achieved by forming a greasein the manner of any of the processes described below and adding more oil to the composition by grinding in a ball mill.
Study of the above table will definitely show that an oil having markedly increased viscosity can be prepared from light oils. A further advantage of oils prepared in accordance with the present invention is their relative stability to temperature change. The following tabledemonstrates this fact by comparison of aerogel containlng oils and untreated oils of comparable viscosity. In this table oil A is a pure SAE No. 20v
lubricating oil. Oil B is SAE No. 10 oil containing 3% by weight of silica aerogel ground in a ball mill for 24 hours. 40 oil, while oil D is a No. 10 oil containing7% by weight of silica aerogel ground for-24 hours.
Oil C is a pure SAE No.
sults in a-grease of-excellent qualities. case with; "thickened normally used at high temperature are especially benefited by lubrication with the present compounded oils.
It has been found desirable to use finely ground aerogel in preparing thickened lubricating oils, since a smoother. more uniform suspension is obtained. Itf'sho'uld be noted in this" connection thata 'larger' amount "or the ground gel is required to give the same results than are gained by a small proportion of the unground aerogel. Incorporation ofta larger amount of aerogel than isrequired to merely thicken the oil re- As is the oils, it is found that the amount of" aerogel required to make a grease of desired qualities varies with the fineness of the w' -aerogel. It has been determined that a good These results indicate quitecleafly aerogel oils demonstrate a stability: toward tem subjected to a range of temperatures or those perature change which is' verydesirable'in lubricants, especially thoseintended for use on'bearings which are idle for periods-.long .-enoughgfor, them to become coldga Moving parts-:whichmre grease may be prepared from motor oil with a viscosity of ten seconds, Saybolt, by incorporation therein of 10% of unground aerogel on the weight of themixture. Iftheaerogel has-been ground one to two hours, about 20% by weight will be required to form a grease of satisfactory consistency, while 30% or more of aerogel ground 20 to 24 hours maybe used;-
A grease of good properties was formedby adding 39 grams of unground aerogel to 350 grams of No. 10 motor oil with vigorous mechanical stirring and subsequently running the resultant slurry through a roller mill several times. The millv used was of the type commonly used togrind paints- It consists of three steel rolls revolving at different speeds. The first and third rolls revolve in the same direction and opposite tov the direction of rotation of the second roll;- the rolls revolve progressively faster in the directionof, the fiowof the material. The shearing action of the rollersserves to grind the oil into the pores of the aerogel, whichv becomes visibly stiffer after the first passage-.throughthe mill and at the end of the sixth pass is found to be a still, transparent, even bodied grease. Such grease is stiff and dry and does not exude oil upon standing for. prolonged periods. c I
For the purposes of comparison, it was attempted to make a grease by adding 30.7%. of fullers earth to a No. 10 oil. The slurry. was as thick as could be agitated practically with the mixing device used viforthe aerogel thickenedoils and greases, but could not be formed into a grease on the roller mill. After'several passes'through' the mill, themixture remained sloppy. and a film of oil separated on top when it wasallowed to stand. I
A test was made to determine'the relative stability of aerogel greases anda good grade'of commercial cup grease to heat. Thecommercial cup grease used for this purpose'was of the type" in whichbody is impartediby the addition- 0f a1 water insoluble soap, while the aerog elgrease" was composed of No.10 motoroiland' 10%- of unground silica] aeroge'h At room temi ieratur ei possesses a'cleaner, moreja'te" grease tractive appearance. "The color "is ,opales'cefriL l o -pa afaegi ch difference bet'ween the two could be detectedin" viscosity. texture, or lubricating qualities.
Samples of the. greases the aerog'el ateri cial grease en" t I and, was
'cosi'ty was" decreased substantially, and the layer. isf'translucentQ No I i v ,were then. placed on watchglasses and heatedtolllilflc. in an oven. 7
detected inithe grease became much shorter than it had been in the cold state.
which may be denominated as petro-gel. Thislatter composition is composed of the original gel structure, with the continuous phase being a petroleum fraction. It is to be understood that gels containing lubricating fluids other than those derived from mineral oil may also be formed, and the following discussion of petrogels is merely illustrative of this feature of the invention.
The liquid continuous phase in a gel may be replaced by another liquid, provided the two liquids are mutually miscible. By employment of that principle, a gel may be prepared in which the continuous phase is a lubricating liquid such as a mineral, vegetable, or animal oil. Exemplary of such gels is the result of replacing the water in a silica gel with acetone, replacing the acetone with textile spirits, and then substituting a petroleum lubricating oil for the textile spirits. Such replacements are accomplished by extraction of the gel with the replacing liquid. If the petroleum oil is a No. lubricant, a grease having desired properties can then be obtained by the incorporation of additional oil on the roller mill.
By similar manipulative steps, a lubricant containing the structure of an organic gel, such as a swelled resin, can be prepared. A sheet of cellulose (Cellophane) was swelled in sodium hydroxide solution, after which the sodium hydroxide was removed by washing with water and the water in turn was displaced by alcohol. The alcohol was then displaced by ether in orderto obtain a liquid phase that is miscible with an oil of mineral or vegetable origin. The ether gel was thereupon washed with a light petroleum lubricating oil whereby the ether was displaced and there resulted a material in sheet form that is suitable for some types of bearings, and packing for bearings, shafts, etc. since it is essentially a relatively firm sheet of soft material consisting predominately of lubricant.
Alternatively, a petro-gel may be formed by immersing in a desired oil, a textile spirits gel,
such as silica gel in which the continuous phase is textile spirits, and distilling off the textile spirits by any suitable method. The preferred method contemplated by this invention is the preparation of a slurry or suspension of textile spirits gel in lubricating oil from which the lighter oil is removed by heating the mixture above the boiling point thereof with agitation. It is to be understood that the invention is not restricted to the use of textile spirits, but rather that any liquid boiling at a temperature substantially below the boiling point of the lubricant may be suitable if miscible with the liquid of the previous step and also with the lubricant.
A petro-gel may be made in various ways other than by an intimate mixing or grinding of an aerogel in a ball mill or,a colloid mill with the petroleum oil, or fraction. One method which has been already indicated consists in displacing the water in a hydro-gel such as a silica hydrogel with alcohol and thereafter displacing the alcohol with a liquid which is miscible with the petroleum fraction as, for example, ether, acetone and the like. The general procedure used is described in my co-pending application, Serial No. 151,969, filed July 3, 1937, and my Patent No.
2,093,454. The resulting acetone gel or ether gel is mixed with a petroleum cut to give the petrogel. The low-boiling liquid may thereafter, if desired, be removedas by distillation as described.
It is to be understood'that this invention is not limited to any specific gel or petro-gel and that aerogels of alumina, tin oxide and the like may be substituted for silica as has previously been indicated. It is likewise to be understood that the lubricants and greases of the present invention may include the present day compounding agents used in this art such as the water-soluble soaps, graphite, fats, and material for improving the oiliness characteristics such as chlorinated hydrocarbons of high boiling point; materials which improve the viscosity index characteristics such as polymerized oleflns of high molecular weight, such as Paratone; corrosion inhibitors: chemical stabilizing agents; pigments and the like may be added to the lubricant within the contemplation of the present invention. I
In lieu of the lubricants of petroleum origin one may substitute wholly or in part vegetable or animal oils as well as synthetic oils such as those obtained by alkylating aromatic hydrocarbons as is well understood by those skilled in the art.
It has been found preferable for some purposes to prepare a thicknened oil from a previously formed grease of the gel to be used in thickening the oil. Vigorous mechanical agitation of the grease with untreated oil results in the formation of an oil having a viscosity intermediate between the viscosities of the grease and the untreated oil.
This invention provides a means of thickening oils and forming greases by incorporation therein of a previously formed gel in substantially the form of the gel as originally prepared. By this means it is possible to use relatively small proportions of thickening agent. A further important advantage lies in the provision of a means to incorporate into the liquid 9. thickening agent of high melting point, in order that the effect of the thickening agent will be retained over a much wider range of temperatures than is possible with thickening agents now used in the preparation of of greases.
This application is a continuation in part of my application, Serial Number 151,969, filed July 3, 1937, now Patent 2,188,007 of January 23, 1940.
I claim:
1. A lubricant comprising an oily liquid substance and a solid substance consisting principally of an inorganic gel formed apart from the liquid substance but'retaining in the thickened liquid the gel structure substantially as formed,
said gel being substantially free from liquids other than said oily liquid substance.
2. A lubricating composition comprising an oily liquid substance and a proportion less than 50% by weight of a substantially water free gel originally formed apart from the said composition in an aqueous medium and characterized by the fact that the structure of the water free gel is substantially that of the gel as originally formed.
consisting of a water immiscible organic oil selected from the group consisting of petroleum hydrocarbons, animal and vegetable oils.
5. A lubricant containing-an oily liquid substance and, in an intimate mixture therewith in anamount suincient to thicken or increase the viscosity of said oily liquid substance, an inorganic aerogel, said lubricant being substantially free 01" water.
6. A thickened lubricant comprising an oily liquid substance and a solid substance consisting principally of a substantially water free gel originally formed apart i'rom the liquid substance in an aqueous medium, said gel retaining in the thickened liquid substance the gel structure substantially as originally formed.
7. A lubricant containing an oily liqui substance and an aerogel in an intimate m ture therewith in an amount suflicient to thicken or increase the viscosity of said oily liquid substance, said lubricant being substantially tree or water.
8. A thickened lubricant comprising an oily liquid substance and a solid substance consisting principally of a substantially water tree .organic gel originally formed apart from the liquid substance in an aqueous medium, said gel retaining in the thickened liquid substance the gel structure substantially as originally formed.
9. A lubricant containing an oily liquid substance and an organic aerogel in an intimate mixture therewith in an amount sumcient to thicken or increase the viscosity of said oily liquid substance, said lubricant being substantially tree of water.
10. A lubricant containing an oily liquid substance and from 10 to 49% by weight or an aerogel based on the weight 01' the mixture, said aerogel being present in an amount sumcient to thicken or increase the viscosity of said liquid substance and form a grease therefrom, and said lubricant being substantially tree of water.
SAMUEL 8. mSTLER.
US184843A 1937-07-03 1938-01-13 Gel and lubricant made therefrom Expired - Lifetime US2260625A (en)

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Cited By (43)

* Cited by examiner, † Cited by third party
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US2455188A (en) * 1946-02-25 1948-11-30 Sun Oil Co Drilling fluid
US2514331A (en) * 1948-06-24 1950-07-04 Standard Oil Dev Co Stabilized lubricating grease
US2554222A (en) * 1947-10-28 1951-05-22 Shell Dev Lubricants
US2563606A (en) * 1951-08-07 Grease containing silica gel treated
US2573650A (en) * 1949-03-22 1951-10-30 Sheil Dev Company Water-resistant greases
US2583603A (en) * 1948-12-18 1952-01-29 Honorary Advisory Council Sci Substituted thickener lubricating grease
US2583606A (en) * 1948-12-18 1952-01-29 Honorary Advisory Council Sci Silica base lubricating greases
US2583604A (en) * 1948-12-18 1952-01-29 Honorary Advisory Council Sci Lubricating grease
US2583607A (en) * 1949-07-01 1952-01-29 Honorary Advisory Council Sci Complex soap greases
US2584085A (en) * 1948-07-20 1952-01-29 Shell Dev Lubricant
US2583605A (en) * 1948-12-18 1952-01-29 Honorary Advisory Council Sci Silica base lubricating grease
US2594822A (en) * 1949-04-16 1952-04-29 Shell Dev Preparation of greases
US2599683A (en) * 1949-05-03 1952-06-10 Shell Dev Grease composition
US2616850A (en) * 1949-11-22 1952-11-04 Standard Oil Co Grease preparation
US2623852A (en) * 1949-12-19 1952-12-30 Shell Dev Oil composition
US2625508A (en) * 1951-02-13 1953-01-13 Shell Dev Water resistant grease
US2626241A (en) * 1949-12-24 1953-01-20 Standard Oil Dev Co Bentonite greases
US2629691A (en) * 1949-12-19 1953-02-24 Shell Dev Grease manufacture
US2635078A (en) * 1950-11-27 1953-04-14 Shell Dev Grease compositions
US2647872A (en) * 1950-01-27 1953-08-04 Shell Dev Grease composition
US2662056A (en) * 1949-06-30 1953-12-08 Gulf Research Development Co Lubricating compositions
US2662057A (en) * 1949-06-30 1953-12-08 Gulf Research Development Co Lubricating compositions
US2668145A (en) * 1951-08-04 1954-02-02 Shell Dev Lubricating compositions
US2676148A (en) * 1950-10-23 1954-04-20 Du Pont Lubricating composition containing surface-esterified siliceous solid
US2677661A (en) * 1950-02-21 1954-05-04 Standard Oil Dev Co Bentonite greases
US2682506A (en) * 1951-10-17 1954-06-29 Ca Nat Research Council Cellulose base lubricating grease
US2710837A (en) * 1949-08-15 1955-06-14 Gulf Research Development Co Lubricating compositions
US2751349A (en) * 1954-05-21 1956-06-19 Pure Oil Co Water resistant lubricants thickened with inorganic gelling agents
US2782165A (en) * 1948-06-01 1957-02-19 Shell Dev Grease compositions
US2810455A (en) * 1955-10-17 1957-10-22 Grace W R & Co Method of dehydrating gases
US2813035A (en) * 1954-03-12 1957-11-12 Deere & Co Waterless green molding sand
US2818346A (en) * 1954-10-04 1957-12-31 Harry G Gossman Compositions for use with electrical connectors
US2850451A (en) * 1954-11-23 1958-09-02 Ca Nat Research Council Lubricating grease containing water repellent aerogel
US2890174A (en) * 1955-02-08 1959-06-09 Gen Dynamics Corp Xerographic developer composition
US2920042A (en) * 1955-03-28 1960-01-05 Texaco Inc Method for preparing water resistant grease and hydrophobic finely-divided solids
US2922703A (en) * 1947-08-01 1960-01-26 Eldon E Bauer Incendiary fuels
US2945809A (en) * 1954-08-05 1960-07-19 Standard Oil Co Thickened lubricant and process for preparing the same
US2948679A (en) * 1953-12-24 1960-08-09 Texaco Development Corp Method of preparing solid-thickened greases
US3047507A (en) * 1960-04-04 1962-07-31 Wefco Inc Field responsive force transmitting compositions
US3117085A (en) * 1953-12-24 1964-01-07 Texaco Development Corp Grease manufacture
US3126259A (en) * 1964-03-24 Incendiary material
US3196109A (en) * 1962-03-01 1965-07-20 Exxon Research Engineering Co Lubricating grease containing boron nitride
US4366075A (en) * 1972-12-29 1982-12-28 Phillips Cables Limited Composition for filling cables

Cited By (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3126259A (en) * 1964-03-24 Incendiary material
US2563606A (en) * 1951-08-07 Grease containing silica gel treated
US2455188A (en) * 1946-02-25 1948-11-30 Sun Oil Co Drilling fluid
US2922703A (en) * 1947-08-01 1960-01-26 Eldon E Bauer Incendiary fuels
US2554222A (en) * 1947-10-28 1951-05-22 Shell Dev Lubricants
US2782165A (en) * 1948-06-01 1957-02-19 Shell Dev Grease compositions
US2514331A (en) * 1948-06-24 1950-07-04 Standard Oil Dev Co Stabilized lubricating grease
US2584085A (en) * 1948-07-20 1952-01-29 Shell Dev Lubricant
US2583604A (en) * 1948-12-18 1952-01-29 Honorary Advisory Council Sci Lubricating grease
US2583606A (en) * 1948-12-18 1952-01-29 Honorary Advisory Council Sci Silica base lubricating greases
US2583605A (en) * 1948-12-18 1952-01-29 Honorary Advisory Council Sci Silica base lubricating grease
US2583603A (en) * 1948-12-18 1952-01-29 Honorary Advisory Council Sci Substituted thickener lubricating grease
US2573650A (en) * 1949-03-22 1951-10-30 Sheil Dev Company Water-resistant greases
US2594822A (en) * 1949-04-16 1952-04-29 Shell Dev Preparation of greases
US2599683A (en) * 1949-05-03 1952-06-10 Shell Dev Grease composition
US2662056A (en) * 1949-06-30 1953-12-08 Gulf Research Development Co Lubricating compositions
US2662057A (en) * 1949-06-30 1953-12-08 Gulf Research Development Co Lubricating compositions
US2583607A (en) * 1949-07-01 1952-01-29 Honorary Advisory Council Sci Complex soap greases
US2710837A (en) * 1949-08-15 1955-06-14 Gulf Research Development Co Lubricating compositions
US2616850A (en) * 1949-11-22 1952-11-04 Standard Oil Co Grease preparation
US2623852A (en) * 1949-12-19 1952-12-30 Shell Dev Oil composition
US2629691A (en) * 1949-12-19 1953-02-24 Shell Dev Grease manufacture
US2626241A (en) * 1949-12-24 1953-01-20 Standard Oil Dev Co Bentonite greases
US2647872A (en) * 1950-01-27 1953-08-04 Shell Dev Grease composition
US2677661A (en) * 1950-02-21 1954-05-04 Standard Oil Dev Co Bentonite greases
US2676148A (en) * 1950-10-23 1954-04-20 Du Pont Lubricating composition containing surface-esterified siliceous solid
US2635078A (en) * 1950-11-27 1953-04-14 Shell Dev Grease compositions
US2625508A (en) * 1951-02-13 1953-01-13 Shell Dev Water resistant grease
US2668145A (en) * 1951-08-04 1954-02-02 Shell Dev Lubricating compositions
US2682506A (en) * 1951-10-17 1954-06-29 Ca Nat Research Council Cellulose base lubricating grease
US3117085A (en) * 1953-12-24 1964-01-07 Texaco Development Corp Grease manufacture
US2948679A (en) * 1953-12-24 1960-08-09 Texaco Development Corp Method of preparing solid-thickened greases
US2813035A (en) * 1954-03-12 1957-11-12 Deere & Co Waterless green molding sand
US2751349A (en) * 1954-05-21 1956-06-19 Pure Oil Co Water resistant lubricants thickened with inorganic gelling agents
US2945809A (en) * 1954-08-05 1960-07-19 Standard Oil Co Thickened lubricant and process for preparing the same
US2818346A (en) * 1954-10-04 1957-12-31 Harry G Gossman Compositions for use with electrical connectors
US2850451A (en) * 1954-11-23 1958-09-02 Ca Nat Research Council Lubricating grease containing water repellent aerogel
US2890174A (en) * 1955-02-08 1959-06-09 Gen Dynamics Corp Xerographic developer composition
US2920042A (en) * 1955-03-28 1960-01-05 Texaco Inc Method for preparing water resistant grease and hydrophobic finely-divided solids
US2810455A (en) * 1955-10-17 1957-10-22 Grace W R & Co Method of dehydrating gases
US3047507A (en) * 1960-04-04 1962-07-31 Wefco Inc Field responsive force transmitting compositions
US3196109A (en) * 1962-03-01 1965-07-20 Exxon Research Engineering Co Lubricating grease containing boron nitride
US4366075A (en) * 1972-12-29 1982-12-28 Phillips Cables Limited Composition for filling cables

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