US2383906A - Improved manufacture - Google Patents

Improved manufacture Download PDF

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US2383906A
US2383906A US463578A US46357842A US2383906A US 2383906 A US2383906 A US 2383906A US 463578 A US463578 A US 463578A US 46357842 A US46357842 A US 46357842A US 2383906 A US2383906 A US 2383906A
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oil
liquid medium
soap
temperature
grease
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US463578A
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John C Zimmer
Arnold J Morway
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Standard Oil Development Co
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Standard Oil Development 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
    • C10M5/00Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D13/00Making of soap or soap solutions in general; Apparatus therefor
    • C11D13/02Boiling soap; Refining
    • C11D13/04Continuous methods therefor
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    • 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
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    • 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
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    • C10M2205/20Natural rubber; Natural resins
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
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    • 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
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    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2207/404Fatty vegetable or animal oils obtained from genetically modified species
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/084Acrylate; Methacrylate
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    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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    • 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
    • C10M2211/024Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aromatic
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    • 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
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    • C10M2211/06Perfluorinated compounds
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
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    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/4981Utilizing transitory attached element or associated separate material
    • Y10T29/49812Temporary protective coating, impregnation, or cast layer

Definitions

  • This4 invention relates to the novel method of manufacturing soap-thickened compositions. More particularly it relates to a continuous process for reacting a saponiable material with a spanonifying agent in the presence of a vliquid medium.
  • the invention comprises continuously mixingtogether proportioned amounts of a liquid medium containing a saponifying agent dispersed therein and effecting this mixing in a high speed mixer in which said two liquids are contacted with each other in a highly turbulent zone,
  • the saponifiable material such as a fatty acid or fat
  • hydrated lime or other suitable saponifying agent is suspended in another portion of mineral lubricating oil and then these two liquids, preferably each preheated to the desired saponica tion temperature, are fed through suitable proportioning equipment, such as metering pumps,
  • a high speed mixer such as a Lancaster disperser 4where the saponiable reaction is completed almost immediately due to the extreme speed and efficiency of the mixing.
  • the liquid medium in which the saponiiiable material and the saponifying agent are separately dissolved or dispersed should be a hydrocarbon liquid having various physical properties, depending upon the intended use of the grease,lsuch as:
  • Viscosity -about 35 to 250 seconds Saybolt Universal at 210 F.
  • V. I. about 5 to 120.
  • Such mineral oil may be derived from various types of crudes, such as paratnic, naphthenic, asphaltlc, etc., and may be subjected to any desiredl type 0f refining. such as distillation, clay treating, acid treating, solvent extraction, etc.
  • the saponiiiable material to be used may be any of the natural or synthetic fats, fatty acids, fatty oils, etc., suitable for use in making lubrieating grease.
  • specific examples of such materials include beef stearin, mutton tallow, hog fat, oleic acid, degras, stearic acid, tallow fatty acids, degras fatty acids, lard oil, rosin, soya bean oil, cottonseed oil, corn oil, neats-foot oil, and similar .animal and vegetable oils or various hydrogenated fatty oils. such as hydrogenated iish oils, or fatty acids.
  • oils derived from such fats and oils as cottonseed oil acid, hydrogenated sh oil acids, etc., or synthetic acids, such as those produced by the oxidation of paraflln'wax.
  • Other grease forming carboxylic acids may be used such as the naphthenic acids derived from petroleum oils, especially those boiling in the range of kerosene, gas oil, or higher fractions.
  • the saponifyng agent may be lime, either in the form of calcium hydroxide, which is preferred, ⁇
  • alkaline earth metal bases such as barium hydroxide or strontium hydroxide or magnesium hydroxide yor -oxide, aluminum hydroxide, lead oxide as well as alkalies, such as lithium, sodium, potassium, rubidium, and cesium, and other known saponifying agents.
  • the saponifying material and the saponifying agent should normally be used in neutralizing proportions although for some purposes. it is desirable'to have a slight excess of acid and for others a slight excess of the saponifying agent.
  • the proportions of oiil and soap in the finished grease'will depend upon the intended use as wellas the types of soap and the viscosity and other characteristics of the lubricating oil, but in general the soap should constitute about Hydres, Snowdotte.
  • the lubricant for the latter use must have a pour point at least as low as 25 F. and must have a ⁇ low temperature co-efiicient, i. e. a low ⁇ viscosity change with temperature, or, in other Words, should have a high viscosity ⁇ index and should be semi-fluidat all times; furthermore, the oil used must not swell rubber, because the grease comes-in contact with rubber bushings and gaskets, 'and the soap should not separate from the oil.
  • the particuar lubricant is preferably composed of about 20% or so of a lime soap of hydrogenated' fish oil acids, and about 60% to 80% of a low pour point aromatic? free coastal lubricating oil, preferably together with a small amount such as 0.5% to 20% ofa soluble organic thickener such as a linear olefinic polymer, e. g. polyisobutylene having a molecu-l lar weight of about 5,000 to 25,000, preferably about 10,000 to 15,000.
  • the hydrogenated fish oil fatty acids are superior to stearic acid for this particular purpose because they contain a substantial proportion of 20 or 22 carbon atoms per molecule as compared to commercial stearic acid which only contains 18 and 16 carbon atom acids.
  • Various grades of hydrogenated ilsh oil acids are available on the market under various trade names, such as Hydrofol, Wyandotte, Weckostear,
  • drogenated sh oil acid having the following pertinent specifications: titre 52 C., free fatty acidl (as oleic) 99%, iodine value 6, saponiiication No. 194 (Hydrofol 51) Itis, of course, understood that the'lubricating greases made may contain a small amount of water or glycerine, either of which may be present as a result of the saponiiication reaction or may be added, if desired.
  • the invention also has many other important applications, such as the production of soapthickened pastes, solid fuel compositions. These may be made, for instance, by thickening an inflammable hydrocarbon oil, such as gasolineand/or kerosene, or even heavier fractions, such as gas oil and lubricating oil, with a suitable object whichmay be sodium stearate, sodium abietate, sodium or calcium soap of hydrogenated fish oils, lithium soaps of stearic acid or hydrogenated fatty oils or acids or the hydrogenated soaps of abietic acid.'
  • various optional addition agents may be used, such as the oil-soluble thickeners of the substantially linear polymer type, e. g., polyisobutylene, polymethacrylate esters, polyvinyl butyl ether, etc., which should have a relatively high molecular weight, e. g., 1,000 to 100,000, or more.
  • organic swelling agents may be used, such as rubber orv synthetic substitutes therefor, although, of course, such materials which are highly unsaturated could only be used where this highl unsaturation, which tends to make the products susceptible to oxidation and gummingwould not be objectionable.
  • Other optional addition agents include amine, ⁇ phenolic or amino phenolic oxidation inhibitors, degras, degras alcohol, saturated or unsaturated alcohols of more than 3 carloonA atoms, glycols, polyglycol, glycol ethers, etc., dyes, pigments,v ⁇ extremel pressure lubricating agents, .airline vor Schiffs base metal deactivators, etc.
  • a liquid medium which is not simply a hydrocarbon liquid but contains other chemical elements, such as, oxygen, halogen, etc., as, for instance, di-butyl phthalate, chlorinated di-phenyl (available on the market under the trade-name arochlor), chlorinated benzene, chlorinated alcohol, chlorinated kerosene, chlorinated parailln wax, ethers, ketones, glycerines, etc.
  • the governing factor 'in determining how much of the oil or other liquid medium should be used in each case, is the desirability of having each of the two liquids of suitable fluidity or consistency for rapid and continuous, i. e. uninterrupted, ow from the supply source through the pipe lines, proportioning equipment, and final mixer.
  • temperatures to be used will, of course, depend primarily upon th'e particular materials used as well as to some extent upon other factors such as the pressure, etc.
  • a temperature of about to 150 F. is desirable for dissolving the 'fatty acid or fatin the lubrieating' oily base stock and the temperature used during the vsaponification will depend primarily upon the type of saponifying agent used as, for
  • the temperature should be from about 120 to 150 F.
  • the temperature i should be about 300 to 500 F.
  • the solution of saponiable material in oil should be either heated or cooled as necessary to bring it tov approximately sap'onication temperature.
  • one of ⁇ these two'liquids maybe preheated to a. temperature sufficiently above the saponification temperature to compensate for the use of the other liquid at a correspondingly lower temperature.
  • soap-thickened compositions are prepared from more volatile hydrocarbon liquids, such as gasoline, or other organic liquids, it may be desirable to carry out the saponiflcation under pressure to avoid undue volatilization.
  • the saponiflcation will generally be carried out under atmospheric or under slightly super-atmospheric pressure, as for instance, up to lbs/sq. in., or so, especially in the case of manufacturing lime soap grease wh'ere it is desirable to retain in the grease some of the water formed by the saponiflcation reaction in order to obtain the desired grease structure.
  • a super-atmospheric pressure of about lbs. to 50 lbs/sq. in., or higher or so should be used with' a corresponding temperature of about 120 to 160 F. when using lime as the sapeiying agent.
  • Sub-atmospheric pressure may be used if it is desired to withdraw water or other lay-products formed during the reaction.
  • the saponiflcation reaction takes place within the high speed mixer 5 and the resultant soapthickened composition issues continuously through line I Il and may, if desired, be passed through a cooler I I, which' is preferably a scraped chiller of the Carbondale type, and preferably the y product is also passed through a filter I2 from whence it is discharged continuously into suitable containers (not shown) for shipment or storage.
  • the supply tank 6 is preferably provided with' a suitable agitator I3 (driven by a suitable source of power not shown) in order to prevent settling of dispersed saponifying agent and in 'order to maintain the dispersion uniform.4
  • a recycling pump I4 in line I and a line I5 for leading the recycled material back into the supply tank 6. If the whole system is operated under superatmospheric pressure, lthen a constant pressure'valve I6 should be provided either in th'e line I0 or at the outlet of the filter I2.
  • the mixer 5 may be any one of a number of high speed mixers in which the materials to be mixed are brought into contact in a highly turbulent zone, whereby eillcient dispersion is obtained by means of the shearing action of rapidly moving parts alone or combined with' the directioning eiect of one or more small vanes or bellies.
  • the preferred type of mixer is a centrifugal pump or a mixer known in the industry as the Lancaster disperser. This latter machine consists essentially of a horizontal operating tube with duplex dispersing mechanism each consisting of two impellers attached to the shaft with a set of stator varies held by tubed wall between impellers.
  • the impellers of one mechanism are of opposite hand to those of the other set, so that the thrust of the two sets of impellers is therefore counterbalanced, practically eliminating end thrust load on th'e bearings.
  • the radial length of the impeller blades is relatively small so that all the material processed is confined to' a thin annular ring where it is vsubjected to a high average peripheral velocity.
  • the machine When operating, the machine is entirely filled with material.
  • the dispersing mechanisms force the material outwardly to the ends of the operating tube and up the end passages to the disperser top.
  • the streams enter the central portion of the top tangentially causing them to -be intimately mixed as they return down the vertical passage to the middle of the operating tube and again enter the dispersing zones to complete recirculation.
  • New feed is added at both sides of the operating tube on to the faces of the irst impellers of each set. Finished product, equal in amount to the new feed, is automatically disch'arged from the center of the disperser top, this material being an intimate mixture of the product from each dispersing mechanism.
  • the effective dispersion obtained in the machine is largely due to the manner in which each ingredient 'iis fed and initially dispersed into a separate stream of mother liquor formed by the space between adjacent blades of the impeller.
  • the streams of fortified product on one side and diluted product on the other are intimately mixed and thoroughly dispersed as they progress through the highly turbulent zones of the dispersingmechanisms.
  • An important feature of this duplex design is that the shaft passes through the body of the machine on the discharge side of the operating mechanism only, thus eliminating any possibility of air infiltration.
  • the disperser is a high speed machine, the shaft running usually at a speed of 3600 revs. per min.
  • a number of dispersers or gear pump equipment similar to colloid mills are available on the market, for example Lancaster dispersers of Model A, series 40 and series 50 or Cornell homogenizers.
  • any mixer or high speed homogenizer may fbe used. These are the ones which :bring the various constituents of the lubricants to be prepared into intimate contact for a short interval. With such high speed mixing. a time of 30 seconds is generally more than sufiicient for eilcient mixing and substantially completes saponiflcation.
  • the solution of saponilable material in the liquid medium, stored in supply tank I is preferably manufactured continuously by continuouslydissolving a suitable fat or fatty acid in controlled proportions in the de sired liquid medium with the application of heat y as required; this heating and dissolving may be eilected continuously by metering the molten fat or fatty acid from a heated storage tank into the liquid medium.
  • the dispersion of saponifying agent in liquid medium as stored in supply tank 6 may be manufactured continuously by continuously feeding the desired saponifying agent, as by means of a screw conveyor in controlled proportions into the ⁇ liquid medium with continuous agitation yand with heat if and to the extent necessary.
  • optional addition agents which are oil-soluble, such as polyisobutylene thickener, as well as variousdyes or anti-oxidants, etc., they are preferably dissolved in the oil which is used for dissolving the saponiable material, although if preferred, such materials could be dissolved in the liquid medium used for dispersing the saponifying agent.
  • the molten sh oil acids and 75% of the mineral oil are blended together at 120 F.
  • the zinc naphthenate and polybutene solution about 8% of polybutene having about 80,000 average molecular weight dissolved in light lubricating oil.
  • the lime is blended in the form of a slurry into the balance of the mineral oil in which the phenyl alpha naphthylamine has been previously dissolved.
  • the separate blends are metered into the disperser or mixing pump and then passed into a screw conveyor when the material is chilled to room temperature and packaged.
  • the rosin oil, rosin, and the Hydrofol acid were dissolved in 3A of the gasoline.
  • the sodium hydroxide in a very fine powder was dispersed in the gasoline, These two mixtures were then metered into the mixing pump or disperser and then packaged, the finished material reaching its final set in the shipping container.
  • Continuous process for making soap-thickened compositions which comprises continuously mixing together at a temperature at least as high as saponiiication temperature proportioned amounts of a non-aqueous liquid medium containing a. saponiable material dissolved therein and a non-aqueous liquid medium non-reactive with a saponifying agent containing a dry saponifying agent dispersed therein, said mixing being eiected in a high speed mixer in which said two liquids are contacted with each other in a highly turbulent zone whereby eiicient dispersion thereof is obtained by means of the shearing action of rapidly moving parts.
  • Continuous process for making lubricating grease which comprises continuously mixing together at about saponiication temperature'proportioned amounts of a mineral lubricating oil containing dissolved therein a saponiiiable fatty material, and a mineral lubricating oil containing a substantially dry saponifying agent dispersed therein, said mixing being effected in a high speed mixer in which said two liquids are contacted with each other in a highly turbulent zone whereby eilicient dispersion thereof isobtained by means ⁇ of the shearing action of rapidly moving parts.
  • Continuous process for making lubricating grease which comprises continuously mixing t0- gether at about F. to 160 F. in a Lancaster disperser proportioned amounts of an aromaticfree coastal lubricating oil containing hydrogenated iish oil acids dissolved therein, and another portion of aromatic-free coastal lubricating oil containing substantially dry hydrated lime dispersed therein.
  • Continuous process for" making a soapthickened composition which comprises continuously dissolving a saponiflable material in controlled proportions in a non-aqueous liquid medium, continuously dispersing a. saponifying agent in controlled proportions in another portion of a non-aqueous liquid medium non reactive with said saponifying agent, and continuously mixing the resultant solution and dispersion in controlled proportions at a temperature at least as high as saponiication temperature, said mixing being effected in a high speed mixer in which said two liquids are contacted with each other in a highly turbulent zone whereby efllcient dispersion thereof is obtained by means of the shearing action of rapidly moving parts.
  • Continuous process for making a soapthickened solid fuel composition which comprises continuously mixing together at a temperature at least as high as saponiiication temperature one portion of an inilammable hydrocarbon liquid containing a soap forming fatty acid dissolved therein, and another portion of an inammable hydrocarbon liquid containing a dry alkali metal hydroxide dispersed therein, said mixing being e'ected in a high speed mixer in which said two liquids are contacted with-each other in a highly turbulent zone whereby eillcient dispersion thereof is obtained by means of lthe shearing action 5 of rapidly moving parts.

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  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
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  • Lubricants (AREA)

Description

Aug- 28, 1945- J. C. ZIMMER ETAL IMPROVED MANUFACTURE Filed oct. 2s, 1942 bawk 3k Patented. Aug. 28, 1945 mrnovnn MANUFACTUBE John C. Zimmer, Union, and Arnold J. Morway, Clark Township, Union County, N. J., assignors to Standard Oil Develo poration of Delaware pment Company, a cor- Appllcation October 28, 1942, Serial No. 463,578
11 Claims.
This4 invention relates to the novel method of manufacturing soap-thickened compositions. More particularly it relates to a continuous process for reacting a saponiable material with a spanonifying agent in the presence of a vliquid medium.
There have been many difficulties involved in the preparation of various soap-thickened organic liquid compositions because the thickening eiect of the soap tends to increase the viscosity rapidly in the immediate vicinity of the reacting particles and tends to produce results which are not uniform. This is partly due to the gel structure of the soap in the presence of the rganic liquid medium and partly due to the fact that the soap constituents are not entirely soluble in the organic liquids.
It has now been found that if the saponiilable material and the saponifying agent, in the presence of the organic liquid medium, are mixed together with sufficient speed and efficiency that the process can be carried out continuously with the production of a uniform product of high quality. Thus it is one objectof the invention to manufacture soap-thickened compositions continuously with great speed and eiciency. Another object of the invention is to carry out thisl continuous manufacture with a minimum lay-out of plant equipment and with a relatively simple, fool-proof design so that the plant can be operated for maximum production with a relatively 'small amount of labor, and with a relatively low requirement of skilled labor and highly technical personnel.
Broadly. the invention comprises continuously mixingtogether proportioned amounts of a liquid medium containing a saponifying agent dispersed therein and effecting this mixing in a high speed mixer in which said two liquids are contacted with each other in a highly turbulent zone,
whereby efficient dispersion thereof is obtained by means of the shearing action of rapidly moving parts.
For example, in applying the invention to the manufacture of a lubricating grease, the saponifiable material, such as a fatty acid or fat, is dissolved in a portion of mineral lubricating oil, and hydrated lime or other suitable saponifying agent is suspended in another portion of mineral lubricating oil and then these two liquids, preferably each preheated to the desired saponica tion temperature, are fed through suitable proportioning equipment, such as metering pumps,
- into a high speed mixer, such as a Lancaster disperser, 4where the saponiable reaction is completed almost immediately due to the extreme speed and efficiency of the mixing.
For the preparation of lubricating greases, the liquid medium in which the saponiiiable material and the saponifying agent are separately dissolved or dispersed, should be a hydrocarbon liquid having various physical properties, depending upon the intended use of the grease,lsuch as:
Flashpoint of 200,to 600 F.
Viscosity,-about 35 to 250 seconds Saybolt Universal at 210 F.
V. I., about 5 to 120.
Such mineral oil may be derived from various types of crudes, such as paratnic, naphthenic, asphaltlc, etc., and may be subjected to any desiredl type 0f refining. such as distillation, clay treating, acid treating, solvent extraction, etc.
The saponiiiable material to be used may be any of the natural or synthetic fats, fatty acids, fatty oils, etc., suitable for use in making lubrieating grease. Specific examples of such materials include beef stearin, mutton tallow, hog fat, oleic acid, degras, stearic acid, tallow fatty acids, degras fatty acids, lard oil, rosin, soya bean oil, cottonseed oil, corn oil, neats-foot oil, and similar .animal and vegetable oils or various hydrogenated fatty oils. such as hydrogenated iish oils, or fatty acids. derived from such fats and oils as cottonseed oil acid, hydrogenated sh oil acids, etc., or synthetic acids, such as those produced by the oxidation of paraflln'wax. Other grease forming carboxylic acids may be used such as the naphthenic acids derived from petroleum oils, especially those boiling in the range of kerosene, gas oil, or higher fractions.
The saponifyng agent may be lime, either in the form of calcium hydroxide, which is preferred,`
or calcium oxide, or other alkaline earth metal bases, such as barium hydroxide or strontium hydroxide or magnesium hydroxide yor -oxide, aluminum hydroxide, lead oxide as well as alkalies, such as lithium, sodium, potassium, rubidium, and cesium, and other known saponifying agents.
The saponifying material and the saponifying agent should normally be used in neutralizing proportions although for some purposes. it is desirable'to have a slight excess of acid and for others a slight excess of the saponifying agent. The proportions of oiil and soap in the finished grease'will, of course, depend upon the intended use as wellas the types of soap and the viscosity and other characteristics of the lubricating oil, but in general the soap should constitute about Hydres, Snowdotte.
5% to 50%, and preferably about 10% to 30%, by' weight of the finished grease. y
One particular type of lubricating grease com- Y bearings, automotive or tractor chassis, air-brake equipment, etc. The lubricant for the latter use must have a pour point at least as low as 25 F. and must have a` low temperature co-efiicient, i. e. a low `viscosity change with temperature, or, in other Words, should have a high viscosity` index and should be semi-fluidat all times; furthermore, the oil used must not swell rubber, because the grease comes-in contact with rubber bushings and gaskets, 'and the soap should not separate from the oil. The particuar lubricant is preferably composed of about 20% or so of a lime soap of hydrogenated' fish oil acids, and about 60% to 80% of a low pour point aromatic? free coastal lubricating oil, preferably together with a small amount such as 0.5% to 20% ofa soluble organic thickener such as a linear olefinic polymer, e. g. polyisobutylene having a molecu-l lar weight of about 5,000 to 25,000, preferably about 10,000 to 15,000. The hydrogenated fish oil fatty acids are superior to stearic acid for this particular purpose because they contain a substantial proportion of 20 or 22 carbon atoms per molecule as compared to commercial stearic acid which only contains 18 and 16 carbon atom acids. Various grades of hydrogenated ilsh oil acids are available on the market under various trade names, such as Hydrofol, Wyandotte, Weckostear,
drogenated sh oil acid having the following pertinent specifications: titre 52 C., free fatty acidl (as oleic) 99%, iodine value 6, saponiiication No. 194 (Hydrofol 51) Itis, of course, understood that the'lubricating greases made may contain a small amount of water or glycerine, either of which may be present as a result of the saponiiication reaction or may be added, if desired.
The present application is a continuation-inpartof said earlier application, Serial No. 415,870,A
filed October 21, 1941, now Patent #2,332,825.
The invention also has many other important applications, such as the production of soapthickened pastes, solid fuel compositions. These may be made, for instance, by thickening an inflammable hydrocarbon oil, such as gasolineand/or kerosene, or even heavier fractions, such as gas oil and lubricating oil, with a suitable object whichmay be sodium stearate, sodium abietate, sodium or calcium soap of hydrogenated fish oils, lithium soaps of stearic acid or hydrogenated fatty oils or acids or the hydrogenated soaps of abietic acid.'
In the various soap-thickened compositions which can be prepared according to this invention, various optional addition agents may be used, such as the oil-soluble thickeners of the substantially linear polymer type, e. g., polyisobutylene, polymethacrylate esters, polyvinyl butyl ether, etc., which should have a relatively high molecular weight, e. g., 1,000 to 100,000, or more. Also organic swelling agents may be used, such as rubber orv synthetic substitutes therefor, although, of course, such materials which are highly unsaturated could only be used where this highl unsaturation, which tends to make the products susceptible to oxidation and gummingwould not be objectionable. Other optional addition agents include amine,` phenolic or amino phenolic oxidation inhibitors, degras, degras alcohol, saturated or unsaturated alcohols of more than 3 carloonA atoms, glycols, polyglycol, glycol ethers, etc., dyes, pigments,v` extremel pressure lubricating agents, .airline vor Schiffs base metal deactivators, etc.
For some purposes, it is satisfactory to use a liquid medium which is not simply a hydrocarbon liquid but contains other chemical elements, such as, oxygen, halogen, etc., as, for instance, di-butyl phthalate, chlorinated di-phenyl (available on the market under the trade-name arochlor), chlorinated benzene, chlorinated alcohol, chlorinated kerosene, chlorinated parailln wax, ethers, ketones, glycerines, etc.
The procedure .to be used in carrying out the present invention may be varied, to some extent,-
part. of which is present then and the rest is continuously blended in later; for satisfactory Vblending in such latter case, it is preferable that at least 20%, and preferably at least 30% or more, of the liquid medium be present during the saponification.
' Of the total amount of lubricating oil or other liquid medium present during the saponification,
. generally about 50 to 90%, preferably 70 to 80% thereof, should be used as the solvent or dis-y persing-agent for the saponifiable material, and
' the remainder as the dispersing medium for the The preferred type is a hysaponifying agent. The governing factor 'in determining how much of the oil or other liquid medium should be used in each case, is the desirability of having each of the two liquids of suitable fluidity or consistency for rapid and continuous, i. e. uninterrupted, ow from the supply source through the pipe lines, proportioning equipment, and final mixer. There should be enough oil with the saponiiiable material to completely dissolve it and make a resulting solution vwhich will flow satisfactorily at the desired saponiiication temperature; generallyY for every one vpart by weight of -saponiable material, about 5 to 9 parts by weight of lubricating oil, gasoline or other suitable liquid medium should be used and similarly for every part by weight of sa-A ponifylng agent, about 3 to 5 parts by Weight of lubricating oil, gasoline or other suitable liquid medium should be used.
The temperatures to be used will, of course, depend primarily upon th'e particular materials used as well as to some extent upon other factors such as the pressure, etc. For instance, in the preparation of lubricating greases generally a temperature of about to 150 F. is desirable for dissolving the 'fatty acid or fatin the lubrieating' oily base stock and the temperature used during the vsaponification will depend primarily upon the type of saponifying agent used as, for
example, for making a. lime soap grease the temperature should be from about 120 to 150 F.,
whereas for a'soda soap grease, the temperature i should be about 300 to 500 F. For best carrysaponifying agent in lubricating'oil should also ybe heated to the saponiiication temperature and the solution of saponiable material in oil should be either heated or cooled as necessary to bring it tov approximately sap'onication temperature. If desired, one of `these two'liquids maybe preheated to a. temperature sufficiently above the saponification temperature to compensate for the use of the other liquid at a correspondingly lower temperature.
Obviously when soap-thickened compositions are prepared from more volatile hydrocarbon liquids, such as gasoline, or other organic liquids, it may be desirable to carry out the saponiflcation under pressure to avoid undue volatilization.
The saponiflcation will generally be carried out under atmospheric or under slightly super-atmospheric pressure, as for instance, up to lbs/sq. in., or so, especially in the case of manufacturing lime soap grease wh'ere it is desirable to retain in the grease some of the water formed by the saponiflcation reaction in order to obtain the desired grease structure. For preparing soap-thickened compositions using gasoline as the liquid medium or as the chief constituent thereof, a super-atmospheric pressure of about lbs. to 50 lbs/sq. in., or higher or so should be used with' a corresponding temperature of about 120 to 160 F. when using lime as the sapeiying agent. Sub-atmospheric pressure may be used if it is desired to withdraw water or other lay-products formed during the reaction.
In order to illustrate the operation of the invention, reference is made to the accompanying drawing which is a schematic lay-out of suitable equipment for carrying out the invention.
Referring to the drawing, a solution of saponiable material in a suitable liquid medium is continuously withdrawn from supply tank .I
through linea and metering pump a via une 4 into the high speed mixer 5 where it is rapidly and intimately mixed with a, dispersion of saponifying agent in a suitable liquid medium, which mixture is continuously withdrawn from supply tank 6 through' line l, metering pump 8, and line 9. The saponiflcation reaction takes place within the high speed mixer 5 and the resultant soapthickened composition issues continuously through line I Il and may, if desired, be passed through a cooler I I, which' is preferably a scraped chiller of the Carbondale type, and preferably the y product is also passed through a filter I2 from whence it is discharged continuously into suitable containers (not shown) for shipment or storage. The supply tank 6 is preferably provided with' a suitable agitator I3 (driven by a suitable source of power not shown) in order to prevent settling of dispersed saponifying agent and in 'order to maintain the dispersion uniform.4
Also, if it is desired to still further insure uniformity in the dispersion of saponifying agent in the liquid medium in supply tank 6, one may provide a recycling pump I4 in line I and a line I5 for leading the recycled material back into the supply tank 6. If the whole system is operated under superatmospheric pressure, lthen a constant pressure'valve I6 should be provided either in th'e line I0 or at the outlet of the filter I2.
The mixer 5 may be any one of a number of high speed mixers in which the materials to be mixed are brought into contact in a highly turbulent zone, whereby eillcient dispersion is obtained by means of the shearing action of rapidly moving parts alone or combined with' the directioning eiect of one or more small vanes or bellies. The preferred type of mixer is a centrifugal pump or a mixer known in the industry as the Lancaster disperser. This latter machine consists essentially of a horizontal operating tube with duplex dispersing mechanism each consisting of two impellers attached to the shaft with a set of stator varies held by tubed wall between impellers. The impellers of one mechanism are of opposite hand to those of the other set, so that the thrust of the two sets of impellers is therefore counterbalanced, practically eliminating end thrust load on th'e bearings. The radial length of the impeller blades is relatively small so that all the material processed is confined to' a thin annular ring where it is vsubjected to a high average peripheral velocity.
When operating, the machine is entirely filled with material. The dispersing mechanisms force the material outwardly to the ends of the operating tube and up the end passages to the disperser top. The streams enter the central portion of the top tangentially causing them to -be intimately mixed as they return down the vertical passage to the middle of the operating tube and again enter the dispersing zones to complete recirculation. New feed is added at both sides of the operating tube on to the faces of the irst impellers of each set. Finished product, equal in amount to the new feed, is automatically disch'arged from the center of the disperser top, this material being an intimate mixture of the product from each dispersing mechanism.
The effective dispersion obtained in the machine is largely due to the manner in which each ingredient 'iis fed and initially dispersed into a separate stream of mother liquor formed by the space between adjacent blades of the impeller. The streams of fortified product on one side and diluted product on the other are intimately mixed and thoroughly dispersed as they progress through the highly turbulent zones of the dispersingmechanisms. An important feature of this duplex design is that the shaft passes through the body of the machine on the discharge side of the operating mechanism only, thus eliminating any possibility of air infiltration. The disperser is a high speed machine, the shaft running usually at a speed of 3600 revs. per min.
A number of dispersers or gear pump equipment similar to colloid mills are available on the market, for example Lancaster dispersers of Model A, series 40 and series 50 or Cornell homogenizers. However, any mixer or high speed homogenizer may fbe used. These are the ones which :bring the various constituents of the lubricants to be prepared into intimate contact for a short interval. With such high speed mixing. a time of 30 seconds is generally more than sufiicient for eilcient mixing and substantially completes saponiflcation.
According to the preferred method of carrying out the invention, the solution of saponilable material in the liquid medium, stored in supply tank I, is preferably manufactured continuously by continuouslydissolving a suitable fat or fatty acid in controlled proportions in the de sired liquid medium with the application of heat y as required; this heating and dissolving may be eilected continuously by metering the molten fat or fatty acid from a heated storage tank into the liquid medium. Likewise the dispersion of saponifying agent in liquid medium as stored in supply tank 6 may be manufactured continuously by continuously feeding the desired saponifying agent, as by means of a screw conveyor in controlled proportions into the` liquid medium with continuous agitation yand with heat if and to the extent necessary.
If optional addition agents are used which are oil-soluble, such as polyisobutylene thickener, as well as variousdyes or anti-oxidants, etc., they are preferably dissolved in the oil which is used for dissolving the saponiable material, although if preferred, such materials could be dissolved in the liquid medium used for dispersing the saponifying agent.
If as previously suggested, it is desirable iirst lto make a soap-thickened concentrate and then Example 1 Formula:
Per cent Hydrogenated fish oil acids 18.0 Hydrated lime 2.64 Low pour Coastal lubricating oil '70.50 Paratac (polybutene solution) '7.85 Zinc naphthenates 0.50
Phenyl alpha naphthylamine 0.50
The molten sh oil acids and 75% of the mineral oil are blended together at 120 F. To this blend is added the zinc naphthenate and polybutene solution (about 8% of polybutene having about 80,000 average molecular weight dissolved in light lubricating oil). The lime is blended in the form of a slurry into the balance of the mineral oil in which the phenyl alpha naphthylamine has been previously dissolved. The separate blends are metered into the disperser or mixing pump and then passed into a screw conveyor when the material is chilled to room temperature and packaged.
Example 2 Formula:
, Per cent Hydrogenated fish oil acids (Hydrofol) 3.50 Rosin oil 6.00
Sodium hydroxide in a dispersion in gasoline 8.75 Rosin 5.00 Gasoline 76.75
The rosin oil, rosin, and the Hydrofol acid were dissolved in 3A of the gasoline. In another tank the sodium hydroxide in a very fine powder was dispersed in the gasoline, These two mixtures were then metered into the mixing pump or disperser and then packaged, the finished material reaching its final set in the shipping container.
It is not intended that this invention be limited to any of the particular examples which are given merely for the sake of illustration but only by the appended claims in which it is intended to claim all novelty inherent in the invention as well as various modifications coming within the scope and spirit of the invention.
We claim:
1. Continuous process for making soap-thickened compositions which comprises continuously mixing together at a temperature at least as high as saponiiication temperature proportioned amounts of a non-aqueous liquid medium containing a. saponiable material dissolved therein and a non-aqueous liquid medium non-reactive with a saponifying agent containing a dry saponifying agent dispersed therein, said mixing being eiected in a high speed mixer in which said two liquids are contacted with each other in a highly turbulent zone whereby eiicient dispersion thereof is obtained by means of the shearing action of rapidly moving parts.
2. Process according to claim 1 in which the mixture of liquids in the vhigh speed mixer has a. temperature at least as high as the saponication temperature and in which the time of actual mixing is not substantially more than about 30 seconds.
3. Process according to claim 1 in which each of the two liquids is preheated to saponification temperature.
4. Process according to claim 1 in which a hydrocarbon liquid is used as the liquid medium both for dissolving the saponiflable material and for dispersing the saponifying agent.
5. Process according to claim 1 in which the high speed mixer used is one of the Lancaster disperser type.
6. Continuous process for making lubricating grease which comprises continuously mixing together at about saponiication temperature'proportioned amounts of a mineral lubricating oil containing dissolved therein a saponiiiable fatty material, and a mineral lubricating oil containing a substantially dry saponifying agent dispersed therein, said mixing being effected in a high speed mixer in which said two liquids are contacted with each other in a highly turbulent zone whereby eilicient dispersion thereof isobtained by means `of the shearing action of rapidly moving parts. v
'7. Process according to claim 6 in which th lubricating oil fed into the high speed mixer with the saponiable material and the saponifying agent constitutes substantially all of the oil present in thel finished lubricating grease.
8. Process according to claim 6 in which only a part of the lubricating oil to be present in the finished grease is used in preparing the solution of saponiiiable material and the dispersion of saponifying agent which are mixed in the high speed mixer, and the remainder of lubricating oil is blended into the mixture after saponiflcation has been completed. f'
9. Continuous process for making lubricating grease which comprises continuously mixing t0- gether at about F. to 160 F. in a Lancaster disperser proportioned amounts of an aromaticfree coastal lubricating oil containing hydrogenated iish oil acids dissolved therein, and another portion of aromatic-free coastal lubricating oil containing substantially dry hydrated lime dispersed therein.
l0. Continuous process for" making a soapthickened composition which comprises continuously dissolving a saponiflable material in controlled proportions in a non-aqueous liquid medium, continuously dispersing a. saponifying agent in controlled proportions in another portion of a non-aqueous liquid medium non reactive with said saponifying agent, and continuously mixing the resultant solution and dispersion in controlled proportions at a temperature at least as high as saponiication temperature, said mixing being effected in a high speed mixer in which said two liquids are contacted with each other in a highly turbulent zone whereby efllcient dispersion thereof is obtained by means of the shearing action of rapidly moving parts.
11. Continuous process for making a soapthickened solid fuel composition which comprises continuously mixing together at a temperature at least as high as saponiiication temperature one portion of an inilammable hydrocarbon liquid containing a soap forming fatty acid dissolved therein, and another portion of an inammable hydrocarbon liquid containing a dry alkali metal hydroxide dispersed therein, said mixing being e'ected in a high speed mixer in which said two liquids are contacted with-each other in a highly turbulent zone whereby eillcient dispersion thereof is obtained by means of lthe shearing action 5 of rapidly moving parts. l
JOHN C. ZIMMER. ARNOLD J. MORWAY.
US463578A 1942-10-28 1942-10-28 Improved manufacture Expired - Lifetime US2383906A (en)

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Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2434539A (en) * 1945-12-22 1948-01-13 Standard Oil Dev Co Lubricants
US2444720A (en) * 1944-10-17 1948-07-06 Shell Dev Manufacture of lithium base greases
US2461276A (en) * 1946-11-12 1949-02-08 California Research Corp Manufacture of soap-thickened compositions and apparatus therefor
US2537039A (en) * 1947-06-12 1951-01-09 Hercules Powder Co Ltd Gelatinous explosive composition
US2610947A (en) * 1950-06-24 1952-09-16 Standard Oil Dev Co Lubricating grease and process of manufacture
US2615396A (en) * 1944-05-22 1952-10-28 Louis F Fieser Munition
US2618536A (en) * 1950-09-20 1952-11-18 Sherwin Williams Co Gel-type fuel and method of making same
US2667457A (en) * 1950-06-30 1954-01-26 Stanolind Oil & Gas Co Method for producing gels
US2675354A (en) * 1950-05-18 1954-04-13 Stanolind Oil & Gas Co Method of producing gels
US2686488A (en) * 1948-01-14 1954-08-17 Harley A Montgomery Method of treating and cold deep drawing sheet metal
US2745810A (en) * 1952-05-02 1956-05-15 Exxon Research Engineering Co Process for preparing lubricating compositions
US2758973A (en) * 1952-05-29 1956-08-14 Exxon Research Engineering Co Process for preparing lubricating grease compositions
US2789040A (en) * 1952-06-20 1957-04-16 Texas Co Process for preparing stable gelled hydrocarbons
US2825694A (en) * 1952-03-25 1958-03-04 Exxon Research Engineering Co Process for the preparation of high temperature anti-friction bearing lubricants
US2850458A (en) * 1956-06-21 1958-09-02 Exxon Research Engineering Co Process for preparing mixed-salt grease compositions
US2892778A (en) * 1954-10-25 1959-06-30 California Research Corp Low temperature method for preparing high temperature greases
US2925387A (en) * 1958-07-21 1960-02-16 Standard Oil Co Method of preparing ureido grease-thickener concentrate and lubricating greases containing same
US2938262A (en) * 1958-07-25 1960-05-31 Quaker Chemical Products Corp Process for the cold reduction of strip metal
US2946751A (en) * 1956-03-26 1960-07-26 Exxon Research Engineering Co Continuous grease manufacture using coated free-flowing alkali metal saponifying agent
US3044959A (en) * 1959-01-15 1962-07-17 Dow Chemical Co Well fracturing
US3475335A (en) * 1963-12-24 1969-10-28 Texaco Inc Method and apparatus for continuous grease manufacture
US3475337A (en) * 1967-05-29 1969-10-28 Texaco Inc Method of grease manufacture
FR2021665A1 (en) * 1968-10-26 1970-07-24 British Petroleum Co
US4392967A (en) * 1981-08-11 1983-07-12 Exxon Research And Engineering Co. Process for continuously manufacturing lubricating grease

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2615396A (en) * 1944-05-22 1952-10-28 Louis F Fieser Munition
US2444720A (en) * 1944-10-17 1948-07-06 Shell Dev Manufacture of lithium base greases
US2434539A (en) * 1945-12-22 1948-01-13 Standard Oil Dev Co Lubricants
US2461276A (en) * 1946-11-12 1949-02-08 California Research Corp Manufacture of soap-thickened compositions and apparatus therefor
US2537039A (en) * 1947-06-12 1951-01-09 Hercules Powder Co Ltd Gelatinous explosive composition
US2686488A (en) * 1948-01-14 1954-08-17 Harley A Montgomery Method of treating and cold deep drawing sheet metal
US2675354A (en) * 1950-05-18 1954-04-13 Stanolind Oil & Gas Co Method of producing gels
US2610947A (en) * 1950-06-24 1952-09-16 Standard Oil Dev Co Lubricating grease and process of manufacture
US2667457A (en) * 1950-06-30 1954-01-26 Stanolind Oil & Gas Co Method for producing gels
US2618536A (en) * 1950-09-20 1952-11-18 Sherwin Williams Co Gel-type fuel and method of making same
US2825694A (en) * 1952-03-25 1958-03-04 Exxon Research Engineering Co Process for the preparation of high temperature anti-friction bearing lubricants
US2745810A (en) * 1952-05-02 1956-05-15 Exxon Research Engineering Co Process for preparing lubricating compositions
US2758973A (en) * 1952-05-29 1956-08-14 Exxon Research Engineering Co Process for preparing lubricating grease compositions
US2789040A (en) * 1952-06-20 1957-04-16 Texas Co Process for preparing stable gelled hydrocarbons
US2892778A (en) * 1954-10-25 1959-06-30 California Research Corp Low temperature method for preparing high temperature greases
US2946751A (en) * 1956-03-26 1960-07-26 Exxon Research Engineering Co Continuous grease manufacture using coated free-flowing alkali metal saponifying agent
US2850458A (en) * 1956-06-21 1958-09-02 Exxon Research Engineering Co Process for preparing mixed-salt grease compositions
US2925387A (en) * 1958-07-21 1960-02-16 Standard Oil Co Method of preparing ureido grease-thickener concentrate and lubricating greases containing same
US2938262A (en) * 1958-07-25 1960-05-31 Quaker Chemical Products Corp Process for the cold reduction of strip metal
US3044959A (en) * 1959-01-15 1962-07-17 Dow Chemical Co Well fracturing
US3475335A (en) * 1963-12-24 1969-10-28 Texaco Inc Method and apparatus for continuous grease manufacture
DE1594633B1 (en) * 1963-12-24 1971-11-04 Texaco Development Corp Process for the continuous production of lubricating greases
US3475337A (en) * 1967-05-29 1969-10-28 Texaco Inc Method of grease manufacture
FR2021665A1 (en) * 1968-10-26 1970-07-24 British Petroleum Co
US4392967A (en) * 1981-08-11 1983-07-12 Exxon Research And Engineering Co. Process for continuously manufacturing lubricating grease

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