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US2084974A - Grease manufacture - Google Patents

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US2084974A
US2084974A US26716A US2671635A US2084974A US 2084974 A US2084974 A US 2084974A US 26716 A US26716 A US 26716A US 2671635 A US2671635 A US 2671635A US 2084974 A US2084974 A US 2084974A
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oil
grease
coil
blend
heated
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US26716A
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Kaufman Gus
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Texaco Inc
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Texaco Inc
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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
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • 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
    • C10N2010/02Groups 1 or 11
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/08Groups 4 or 14
    • 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
    • C10N2050/10Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
    • 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
    • C10N2070/00Specific manufacturing methods for lubricant compositions

Definitions

  • Lauer No. 1,912,001 discloses a continuous process of manufacturing grease, wherein a mixture of mineral oil and fatty oil is passed through a preheating section of a coil 10 heater, then alkaline or saponifying material is introduced intovthe preheated mixture and the d latter is flowed through a further section of the heating coil for saponlfication, followed by introducing the heated mass into a chamber where water vapors and other undesirable vapors may be removed to produce a desired final product.
  • the present invention constitutes an improvement on the method of the above mentioned Lauer patent, which is particularly adaptable to the manufacture of a substantially dehydrated high melting point soda base grease of the character of driving journal compound. It has been heretofore considered that a satisfactory grease of this type could' not be effectively produced by such la continuous process.
  • a mixture of mineral oil and fatty oil is flowed together with air in a connned stream, such as through a pipe still heating coil, wherein it is 40 heated to a high temperature above the melting point of the final product.
  • the heating in the presence of air isfthen continued; for' example, in an enlarged conversion chamber, until a predetermined increase in viscosity of the mineral oil-fatty oil blend occurs.
  • the blend is nowed together with saponifying material through a further heating coil and iinally flashed into an enlarged zone from where vapors are withdrawn to produce the final product.
  • a charge pump III withdraws a blend of mineral oil and fatty oil from a storage tank I I, and delivers the same through line I2 to a heating coil I3 within a pipe still heater I4. Air under pressure is introduced into line I2 by the branch line I5, so as to pass along with the oil-fat blend.
  • the petroleuin or hydrocarbon lubricating oil may be of the nature of a cylinder stock and may embrace either a distillate or a residual product derived from either a paratlin or naphthene base, or mixed paraffin and naphthene base crudes, or maybe of the nature of a pale oil or a fraction of lower boiling range than cylinder oil derived from any of the foregoing crude sources.
  • the fatty oil or fatty acid may be derived from either animal or vegetable origin, such as hard tallow, tallow oil, iieshing ⁇ grease, stearin, elaine oil, castor oil, cottonseed oil, residual pitchy material resulting from the destructive distillationof fatty oils and fatty acids, and may also embrace hydrogenated fats.
  • a blend of cylinder stock and hard tallow is preferred for this purpose.
  • the proportions of the mineral oil and fatty oil may vary within considerable limits, although it is generally preferred to provide a soap content in the finished grease of around 40 to 50%. However, the soap content may be considerably reduced, for ex.- ample, to as low as 20 to 25%, and by'a conversion process as described in my Patent No. 1,966,821, a satisfactory hard grease of the proper penetration still obtained.
  • the heating coil I3 is preferably raised to a temperature in excess of the melting point of the i'lnal product; for example, in excess of 400 F.
  • temperatures for example, in excess of 400 F.
  • temperatures of the order of 400400 F., although higher temperatures up to around 750 F. may be used.
  • the preheated mixture is discharged from the coil I3 by line I6 into an enlarged conversion chamber II provided with staggered banles I8, and equipped with a re box I9 so as to maintain the temperature of the heated mix during a reasonably prolonged storage therein.
  • the conversion chamber Cal may be provided with an additional air coil for blowing the heated mixture with air during its storage therein to attain a more rapid viscosity increase. It is generally desirable to produce a viscosity increase in excess of 20%, generally an increase of about 2060% being attained.
  • the time of heating in the coil I3 and conversion chamber Il will, of course, vary with the temperature employed, higher temperatures requiring less time for a predetermined viscosity increase and vice versa.
  • the conversion chamber may be omitted when the coil heater gives the desired conversion. Ordinarily, a total heating time of the order of about 4-8 hours in the presence of air is satisfactory.
  • the conversion chamber may be provided with a vapor offtake 2
  • the receiver is provided with a vent line 24 leading to a steam jet 25 to provide suction to withdraw the vapors through the condensing apparatus.
  • These condensed products may be returned to the system, or may be employed in the manufacture of other greases.
  • the conversion chamber Il is preferably of such size, and is so coordinated with the charge rate, that the desired conversion time for the mineral oil-fatty oil blend is attained as the latter fiows through the tortuous or baffled passage within this chamber to the discharge line 26.
  • a booster pump 2l is preferably positioned within this line 2S, and delivers the heated material to an additional heating coil 28 within the furnace I4, although it is obvious that a separate furnace can be employed.
  • Saponifying material such as caustic soda solution
  • a tank 30 is supplied from a tank 30 through line 3I to calibrated feeder tanks 32, from where it is withdrawn by a proportioning pump 33 and delivered by line 34 to one or more pipe lines 35 discharging into ⁇ coil 28 at different positions along the length of this coil.
  • the caustic soda solution so supplied is proportioned in accordance with the charge rate so as to just supply sufficient caustic soda for saponification of the saponifiable content of the fatty oil, and preferably to provide a slight excess of free alkali,
  • the coil 28 is heated to a temperature in excess of 400 F. and below 800 F., preferably a range of around BOO-'750 F. being employed. While caustic soda is generally preferred, other saponifying materials, such as lime, litharge, magnesia, etc., may be employed.
  • the heated mixture is then discharged by line 3l into an expansion drum 38 equipped with an agitator 39 where vapors including water, glycerine and any volatile decomposition products flash off. These vapors are withdrawn through vapor outlet 40 equipped with reflux coil 4I, the non-condensed vapors passing by vapor line 42 to water cooled condenser 43, from Where the condensate is discharged into receiver 44.
  • the final product from expansion chamber 38 is discharged by line 46 to a water or steam cooled screw pump 4l, which discharges the cooled grease through a mold 4B, which forms it into cakes of predetermined size. These cakes may be discharged into individual containers 49 carried by a traveling belt conveyor 50 to a point of discharge.
  • the system may be operated at atmospheric or superatmosphcric pressures, or under vacuum.
  • a blend of by weight of cylinder stock and 45% by weight of tallow was passed through the heating coil I3 together with an excess of air at substantially atmospheric pressure, with a heater outlet temperature of M50-520 F. and a conversion chamber temperature of around 400- -440 F.
  • the tests on the charge or blend before and after treatment were as follows:
  • the penetration or hardness of the resulting grease is expressed in terms of tenths of a mm. penetration of an average sample as determined by ⁇ the standard A. S. T. M. penetrometer and method for greases (see test D-217-27-T), except that the same apparatus is modified to the extent of having an extra weight of 475 g. placed within the penetrometer cone. Such reading is termed penetration, modified A. S. T. M. This modified penetration test has been used on samples of relatively hard products to penetrate more deeply and give a higher and more accurate reading than that obtained with the same apparatus without the added weight.
  • the present method of continuous manufacture possesses certain advantages over the customary batch manufacture. For example, loss of fat due to volatilization during heating is avoided in the closed system, so that a smaller quantity of fat for the same soap content may be employed. Furthermore, a shorter treating time with greater output is generally attained in the continuous manufacture. In addition, greater uniformity due to better control of manufacture is obtained; also, less space is required for such a continuous grease manufacturing unit.y
  • a continuous process for manufactm'ing grease which comprises lowing a mixture of minerai oil and fatty oil" through a heating coil wherein the mixture is heated to a high temperature above the melting point of the final product.

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

Description

11.111622, 1937. G, KAUFMAN GREASE MANUFACTURE Filed June 15, 19:55y
Patented June 22, 1937" y-UNlTED STATES GREASE MANUFACTUBE Gus Kaufman, Beacon, N. Y., asslgnor to The Texas Company, New York, N. Y., a corporation of Delaware Application June 15, 1935, Serial No. 26,716
1 Claim.
'I'his invention relates to the continuous manufacture of grease, and particularlyAa grease of the substantially dehydrated soda base type adapted for the lubrication of locomotive driving 5 Journals.
The patent to Lauer No. 1,912,001 discloses a continuous process of manufacturing grease, wherein a mixture of mineral oil and fatty oil is passed through a preheating section of a coil 10 heater, then alkaline or saponifying material is introduced intovthe preheated mixture and the d latter is flowed through a further section of the heating coil for saponlfication, followed by introducing the heated mass into a chamber where water vapors and other undesirable vapors may be removed to produce a desired final product.
The present invention constitutes an improvement on the method of the above mentioned Lauer patent, which is particularly adaptable to the manufacture of a substantially dehydrated high melting point soda base grease of the character of driving journal compound. It has been heretofore considered that a satisfactory grease of this type could' not be effectively produced by such la continuous process.
I have discovered that when a blend of the' mineral oil-fatty oil is heated in the presence of air, or with the addition of air to the closed system or heating coil, and the oil-fat blend is preheated for an' appreciable time to produce certain chemical and physical changes in the material,
as evidenced by a predetermined increase in viscosity, before the addition of the saponifying material, a satisfactory product can be produced in a continuous process of this character.
In accordance with the present invention, a mixture of mineral oil and fatty oil is flowed together with air in a connned stream, such as through a pipe still heating coil, wherein it is 40 heated to a high temperature above the melting point of the final product. The heating in the presence of air isfthen continued; for' example, in an enlarged conversion chamber, until a predetermined increase in viscosity of the mineral oil-fatty oil blend occurs. Then the blend is nowed together with saponifying material through a further heating coil and iinally flashed into an enlarged zone from where vapors are withdrawn to produce the final product.
The invention may be clearly understood from the following detailed description, taken with reference to the accompanying drawing which illustrates dlagrammatlcally a preferred embodiment of apparatus for practicing the method of 55 this invention:
A charge pump III withdraws a blend of mineral oil and fatty oil from a storage tank I I, and delivers the same through line I2 to a heating coil I3 within a pipe still heater I4. Air under pressure is introduced into line I2 by the branch line I5, so as to pass along with the oil-fat blend. Where a grease of the character of driving jour-` nal compound is being manufactured, the petroleuin or hydrocarbon lubricating oil may be of the nature of a cylinder stock and may embrace either a distillate or a residual product derived from either a paratlin or naphthene base, or mixed paraffin and naphthene base crudes, or maybe of the nature of a pale oil or a fraction of lower boiling range than cylinder oil derived from any of the foregoing crude sources. The fatty oil or fatty acid may be derived from either animal or vegetable origin, such as hard tallow, tallow oil, iieshing` grease, stearin, elaine oil, castor oil, cottonseed oil, residual pitchy material resulting from the destructive distillationof fatty oils and fatty acids, and may also embrace hydrogenated fats. A blend of cylinder stock and hard tallow is preferred for this purpose. The proportions of the mineral oil and fatty oil may vary within considerable limits, although it is generally preferred to provide a soap content in the finished grease of around 40 to 50%. However, the soap content may be considerably reduced, for ex.- ample, to as low as 20 to 25%, and by'a conversion process as described in my Patent No. 1,966,821, a satisfactory hard grease of the proper penetration still obtained.
'Ihe mixture flowing through the heating coil I3 is preferably raised to a temperature in excess of the melting point of the i'lnal product; for example, in excess of 400 F. Thus, very satisfactory results may be secured by employing temperatures of the order of 400400 F., although higher temperatures up to around 750 F. may be used. It is found desirable to produce a predetermined increase in viscosity of the mineral oil-fatty oil blend prior to saponiilcation. While the desired conversion as indicated by a predetermined increase in viscosity can be secured by passing through the heating coil, the length ofthe coil can be materially reduced by means of an auxiliary heated conversion chamber. In accordance with the presentprocess, the preheated mixtureis discharged from the coil I3 by line I6 into an enlarged conversion chamber II provided with staggered banles I8, and equipped with a re box I9 so as to maintain the temperature of the heated mix during a reasonably prolonged storage therein. The conversion chamber Cal may be provided with an additional air coil for blowing the heated mixture with air during its storage therein to attain a more rapid viscosity increase. It is generally desirable to produce a viscosity increase in excess of 20%, generally an increase of about 2060% being attained. The time of heating in the coil I3 and conversion chamber Il will, of course, vary with the temperature employed, higher temperatures requiring less time for a predetermined viscosity increase and vice versa. Also, the conversion chamber may be omitted when the coil heater gives the desired conversion. Ordinarily, a total heating time of the order of about 4-8 hours in the presence of air is satisfactory. The conversion chamber may be provided with a vapor offtake 2| equipped With a cooling coil 22 for refiuxing back to the chamber, uncondensed vapors passing through vapor line 23 to a water cooled condenser 24 and thence to a receiver 25. The receiver is provided with a vent line 24 leading to a steam jet 25 to provide suction to withdraw the vapors through the condensing apparatus. These condensed products may be returned to the system, or may be employed in the manufacture of other greases.
The conversion chamber Il is preferably of such size, and is so coordinated with the charge rate, that the desired conversion time for the mineral oil-fatty oil blend is attained as the latter fiows through the tortuous or baffled passage within this chamber to the discharge line 26. A booster pump 2l is preferably positioned within this line 2S, and delivers the heated material to an additional heating coil 28 within the furnace I4, although it is obvious that a separate furnace can be employed.
Saponifying material, such as caustic soda solution, is supplied from a tank 30 through line 3I to calibrated feeder tanks 32, from where it is withdrawn by a proportioning pump 33 and delivered by line 34 to one or more pipe lines 35 discharging into `coil 28 at different positions along the length of this coil. The caustic soda solution so supplied is proportioned in accordance with the charge rate so as to just supply sufficient caustic soda for saponification of the saponifiable content of the fatty oil, and preferably to provide a slight excess of free alkali, The coil 28 is heated to a temperature in excess of 400 F. and below 800 F., preferably a range of around BOO-'750 F. being employed. While caustic soda is generally preferred, other saponifying materials, such as lime, litharge, magnesia, etc., may be employed.
The heated mixture is then discharged by line 3l into an expansion drum 38 equipped with an agitator 39 where vapors including water, glycerine and any volatile decomposition products flash off. These vapors are withdrawn through vapor outlet 40 equipped with reflux coil 4I, the non-condensed vapors passing by vapor line 42 to water cooled condenser 43, from Where the condensate is discharged into receiver 44.
The final product from expansion chamber 38 is discharged by line 46 to a water or steam cooled screw pump 4l, which discharges the cooled grease through a mold 4B, which forms it into cakes of predetermined size. These cakes may be discharged into individual containers 49 carried by a traveling belt conveyor 50 to a point of discharge.
While air is preferably introduced by the line I5 into coil I3, it is to be understood that under some conditions the introduction of air may be delayed until the preheated mineral oil-fatty oil blend has been discharged into the conversion chamber I'l. It is also possible to by-pass the coil I3 and carry out the conversion and heating of the fatty oil-mineral oil blend entirely in the conversion chamber I`I. The system may be operated at atmospheric or superatmosphcric pressures, or under vacuum.
As a specific example of the present invention, a blend of by weight of cylinder stock and 45% by weight of tallow was passed through the heating coil I3 together with an excess of air at substantially atmospheric pressure, with a heater outlet temperature of M50-520 F. and a conversion chamber temperature of around 400- -440 F. The tests on the charge or blend before and after treatment were as follows:
Charge before Charge after Acid number 'I'he conversion product was then passed through coil 28 together with caustic soda solution employing a heater outlet temperature of 680 F., with a bottom temperature in expansion drum 3B of 525 F. and a vapor outlet temperature of 490 F. A hard uniform dehydrated grease was secured having the following tests:
Penetration-Modified A. S. T. M 77 Melting point-Dropping point method- 419 F. Soda soap 43.5%
In the above specific example, the penetration or hardness of the resulting grease is expressed in terms of tenths of a mm. penetration of an average sample as determined by`the standard A. S. T. M. penetrometer and method for greases (see test D-217-27-T), except that the same apparatus is modified to the extent of having an extra weight of 475 g. placed within the penetrometer cone. Such reading is termed penetration, modified A. S. T. M. This modified penetration test has been used on samples of relatively hard products to penetrate more deeply and give a higher and more accurate reading than that obtained with the same apparatus without the added weight.
Melting points referred to herein are comparable to those taken by the method described on pages 105-107 of the article entitled Lubrication and Lubricants by G. R. Roland, Journal of the American Society of Naval Engineers, vol. 3l, 1919. This method or slight modifications thereof has been widely used with success for many years by grease chemists, and is frequently referred to as the dropping point method.
It is pointed out that the present method of continuous manufacture possesses certain advantages over the customary batch manufacture. For example, loss of fat due to volatilization during heating is avoided in the closed system, so that a smaller quantity of fat for the same soap content may be employed. Furthermore, a shorter treating time with greater output is generally attained in the continuous manufacture. In addition, greater uniformity due to better control of manufacture is obtained; also, less space is required for such a continuous grease manufacturing unit.y
Obviously many modifications and variations of the invention, as hereinbefore set forth, may be made without departing Y from the spirit and scope thereof. and therefore only such limitations should be imposed as are indicated in the ap pended claim.
I claim: A
A continuous process for manufactm'ing grease which comprises lowing a mixture of minerai oil and fatty oil" through a heating coil wherein the mixture is heated to a high temperature above the melting point of the final product. introducingairintotheheatingcoilsoastopass through uw con um; with the minerai ou-fatty oil blend, discharging the'Amixture into an en-I larged reaction sone where it is further blown with air while -the high temperature thereof ismaintained until a predetermined increase in viscosity of the mineral oil-fatty oil blend occurs,
- then further flowing the mineral oil-fatty oil blend together with saponifying material through a heating coil wherein it is heated to a hightemperature, nnallyflashing the heated material into an enlarged none, withdrawing from the zone vapors evolved therein, and removing from the none the desired nnalproduct;
GUS
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2417495A (en) * 1943-12-10 1947-03-18 Girdler Corp Manufacture of grease
US2433636A (en) * 1942-02-20 1947-12-30 Benjamin Clayton Manufacture of greases
US2483282A (en) * 1945-09-15 1949-09-27 Girdler Corp Art of grease manufacture
US2484328A (en) * 1947-07-01 1949-10-11 Spencer Kellogg And Sons Inc Method of modifying castor oil
US2495651A (en) * 1947-03-20 1950-01-24 Socony Vacuum Oil Co Inc High-temperature ball-bearing grease
US2578366A (en) * 1945-02-23 1951-12-11 Procter & Gamble Continuous process for neutralizing fatty acids
US2626898A (en) * 1950-10-26 1953-01-27 Texas Co Process for preparing alkali metal greases
US2842495A (en) * 1954-11-22 1958-07-08 Exxon Research Engineering Co Process for forming high salt content complex greases
US2916453A (en) * 1955-12-22 1959-12-08 Texaco Inc Manufacture of sodium base grease

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2433636A (en) * 1942-02-20 1947-12-30 Benjamin Clayton Manufacture of greases
US2417495A (en) * 1943-12-10 1947-03-18 Girdler Corp Manufacture of grease
US2578366A (en) * 1945-02-23 1951-12-11 Procter & Gamble Continuous process for neutralizing fatty acids
US2483282A (en) * 1945-09-15 1949-09-27 Girdler Corp Art of grease manufacture
US2495651A (en) * 1947-03-20 1950-01-24 Socony Vacuum Oil Co Inc High-temperature ball-bearing grease
US2484328A (en) * 1947-07-01 1949-10-11 Spencer Kellogg And Sons Inc Method of modifying castor oil
US2626898A (en) * 1950-10-26 1953-01-27 Texas Co Process for preparing alkali metal greases
US2842495A (en) * 1954-11-22 1958-07-08 Exxon Research Engineering Co Process for forming high salt content complex greases
US2916453A (en) * 1955-12-22 1959-12-08 Texaco Inc Manufacture of sodium base grease

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