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US2431008A - Cooling fluid - Google Patents

Cooling fluid Download PDF

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Publication number
US2431008A
US2431008A US502462A US50246243A US2431008A US 2431008 A US2431008 A US 2431008A US 502462 A US502462 A US 502462A US 50246243 A US50246243 A US 50246243A US 2431008 A US2431008 A US 2431008A
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molecular weight
viscosity
vinyl
polymer
grinding
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US502462A
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Donald L Wright
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Standard Oil Development Co
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Standard Oil Development Co
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M3/00Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/062Oxides; Hydroxides; Carbonates or bicarbonates
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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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    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/06Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
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    • 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
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    • 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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    • C10N2040/20Metal working
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Definitions

  • This invention relates to a novel cooling fluid, and more particularly to the use thereof in the machining of metals, especially for high speed grinding of threads and the like.
  • One object of the present invention is to provide a cooling fluid which will be more eflicient in the cooling operation. Another object of this invention is to accomplish this superior cooling without any attendant sacrifice of lubricating 30,000, 60,000, 80,000, 100,000, etc.
  • the invention comprises using as a cooling fluid a composition comprising a major proportion of a volatile organic liquid of relatively low viscosity and containing dissolved therein a minor proportion of a viscosity-increasing high molecular weight linear essentially aliphatic polymer which, upon subjection to elevated temperature, is capable of depolymerizing and vaporizing without substantial carbonization or tar formation.
  • a minor proportion of one or more oiliness or anti-sieze agents are examples of one or more oiliness or anti-sieze agents.
  • the volatile organic liquid to be used should be one boiling below about 750 F. and may suit ably be a light petroleum distillate boiling below the lubricating oil boiling range as, for instance, mineral seal oil or kerosene.
  • mineral seal oil or kerosene may be a mineral seal oil having a boiling range from about filo-670 F., or 500-700 F., or a kerosene boiling from about 350-500 F., or 355-5l0 F., etc.
  • plain hydrocarbon liquid one may use various oxygenated compounds, halogenated compounds, etc., or derivatives thereof.
  • the primary object in using the above described types of volatile liquid as the cooling fluid of this invention is to make use of the latent heat of evaporation rapidly to absorb the heat of abrasion.
  • the substance to be used in this capacity should be substantially non-toxic and non-corrosive both in the liquid state and vapor state, for of course during the grinding operations a substantial amount of this volatile liquid is vaporized at the point of grinding.
  • polyisobutylene having an average molecular weight above 800 and preferably about 2000, such as 5,000 or 10,000, although if desired isobutylene polymers having even considerably higher molecular weights may be used, such as In general,
  • polymers having an average molecular weight between-about 2,000 and 15,000 or 20,000 are available at lower cost than the higher molecular weight ones and serve at least as well for the purposes of this invention, or perhaps even better than polymers having molecular weights of 30,000 or above.
  • Other polymerized iso-oleflns having similar characteristics may be used, for instance, polymerized isoamylene, e. g., polymerized methyl 2 butene 1, etc.
  • Qther hydrocarbon polymers which may be used as thickeners include high molecular weight plastic or solid polyethylene, or similar plastic or solid copolymers such as a copolymer of isobutylene and ethylene, made for instance at 100-400" C.
  • isobutylene-diolefin copolymers ranging, for instance, from 5,000 to 50,000 or more, such as made by copolymerizing a mixture of 90% of isobutylene and 10% butadiene at 103 C. using liquid ethylene as refrigerant and using a solution of aluminum chloride in ethyl chloride as catalyst.
  • Such additives include polymers of vinyl ethers having the general formula:
  • R1 is an unsubstituted or substituted aliphatic, aromatic, or hydroaromatic radical
  • R2 is a hydrogen atom or a substituted or unsubstituted aliphatic radical, e, g., vinyl oleyl ether, vinyl isobutenyl ether, vinyl meta-cresyl ether, vinyl cyclohexyl ether, vinyl octadecyl ether, vinyl chloroethyl ether, vinyl amino propyl ether, a-ethylvinyl isohexyl ether, a-chloromethyl vinyl lauryl ether, etc.; polymers of vinyl esters having the general formula in which R1 and R2 are as above and n is an integer having a value of 1 or more, e.
  • vinyl stearate vinyl ester of acids obtained by oxidation of paraifin wax, vinyl chloropropionate, vinyl aminopalmitate, vinyl adipate, vinyl citrate, etc.
  • polymers of acrylic acid esters having the general formula, ROOCC(X) CH2, in which R is an unsubstituted or substituted aliphatic, aromatic, or hydroaromatic group, preferably containing at least 10 carbon atoms, and X is a H or a halogen atom, or 2. CH3 group or a C2H5 group, e.
  • lauryl acrylate g., lauryl acrylate, cetyl acrylate, octadecyl acrylate, amylphenyl methacrylate, isoheptyl cyclohexyl chloroacrylate, chlorodecyl methacrylate, etc., especially such polyacrylic esters having a molecular weight of 5,000 to 10,000.
  • R is a H atom or an unsubstituted or substituted aliphatic, aromatic, or hydroaromatic group
  • :n and 3 may equal or any integer provided that :c+y equals at least 5, and where n is 0 or an integer and m is a whole number and Z is a functional group which has one replaceable hydrogen atom, Z being capable of esterifying a carboxyl group.
  • oiliness agent or anti-freeze agent one may use various materials known to the art such as oleic acid, tricresyl phosphate, isopropyl esters of wax oxidation acids and soda.
  • the viscosity-increasing polymer in carrying out the invention it is desirable to use a sufficient amount of the viscosity-increasing polymer to raise the viscosity of the volatile liquid from a value in the range from about 30 to 50 seconds Saybolt at F. up to a viscosity in the range of about -500 seconds Saybolt at 100 F., preferably about 200-4500 seconds at 100 F.
  • the amount of polymer or thickener required for this purpose will not only depend upon the exact viscosity desired in the finished blend, but will also depend upon the molecular weight of the polymer, as well as the individual thickening ability of the particular polymer used which varies slightly according to the chemical structure of the polymer.
  • a lauryl alpha methacrylate polymer having an average molecular weight of about 10,000 will be required in a concentration of about 11% to raise the viscosity of the mineral seal oil to 150 seconds Saybolt at 100 F., but only about 7% will be required of a 16,000 average molecular weight lauryl alpha methacrylate polymer.
  • the amount of polymer to be used will ordinaril range from about 1-20%, generally about 2-15% by weight.
  • oiliness agent to be used will depend primarily upon the type of such agent used, but will ordinarily range from about .02 to 10%, preferably about 1-5%. about 3-8% or so of oleic acid may be used,
  • a blend was prepared having the following composition:
  • This blend was used as a cooling fluid on a high speed tap grinding machine operating at a spindle speed of 2400 R. P. M. using a Norton abrading wheel 7" x 12" x A", the tap of which had a diameter of 1.25 cm. (less than 0.500 diameter) and was made of special steel having a Rockwell hardness of 064-66, and was provided with a Whitworth full English thread.
  • the oil blend had a viscosity of 202 seconds at 100 F.
  • the room temperature was 72 F. and the temperature of the oil in the machine was 80 F.
  • a thread grinding operation was accomplished in two passes, one a rough pass of 0.030", and one a finished pass of 0.003".
  • liquid a substantial proportion of which is vaporizable by the heat of abrasion, and a minor portion up to about 20% by weight of an aliphatic polymeric thickener adapted to decompose at elevated temperatures without leaving any substantial residue, said thickener being a high molecular weight viscosity-increasing polymer having an average molecular weight of not less than 800.
  • the method of carrying out high speed grinding operations in which an abrading wheel rotates at high speed against metal stock and generates a large amount of heat which comprises applying to the metal stock at the point of abrasion a viscous lubricant comprising a major portion of a petroleum distillate boiling between about 350 and 750 F. a substantial proportion of which is vaporized by the heat of abrasion and a minor portion of about 1 to 20% by weight of a substantially saturated aliphatic polymer having a molecular weight of at least 1000 dissolved in said distillate to make a solution having a viscosity between about 150 and 500 seconds Saybolt at F.
  • the method of carrying out high speed thread grinding operations by grinding a thread in a piece of steel stock by an abrading wheel rotating at high speed which comprises applying to the steel at the point of abrasion a cooling fiuid consisting essentially of about 92-93% of mineral seal oil, about 2.5% of polyisobutylene having an average molecular weight of about 60,000, and about 5% of oleic acid.

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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

Patented Nov. 18, 1947 COOLING FLUID Donald L. Wright, Weatfleld, N. 1.. ulignor to Standard Oil Development Company, a corporation of Delaware No Drawing. Application September 15, 1943 Serial No. 502,462
4 Claims. 1
This invention relates to a novel cooling fluid, and more particularly to the use thereof in the machining of metals, especially for high speed grinding of threads and the like.
A relatively recent development in the machining of metals is the use of high speed grinding by a rotary grinding wheel instead of the more conventional cutting of threads, taps. etc. in the metal by special alloy cutting tools. High speed grinding of threads on a bolt, for instance, is considerably faster than the cutting operations required to produce the same threads. This high speed grinding has the additional advantage of eliminating the use of cutting tools made of special steel or other alloys which are either extremely expensive or diflicult to secure, which are required to withstand the high temperatures to which the point of the cutting tool is exposed, particularly when cutting operations are speeded up in order to increase production.
However, it is apparent that even more heat is evolved during high speed grinding operations than during corresponding cutting operations and therefore the heat of abrasion must be removed very rapidly in order to prevent burning of the metal parts being machined. Attempts have been made thus far to solve this problem by feeding conventional cutting oil at the grinding point for the combined purpose of removing the heat of abrasion and to remove finely divided particles of metal taken out by the abrading wheel, together of course with any particles of abrading material which may incidentally be loosened from the abrading wheel during the operation. The lubricant or grinding oil must possess the ability adequately to cool the parts. to lubricate and not to build up on or to load the grinding wheel. These requirements are quite severe and most of the conventional cutting oils (mineral oil, fatty oil and sulfur) are not satisfactory as grinding oils because of failure to perform one or more of the necessary functions, chiefly because of inability sufficiently to cool the metal at the immediate point and instant of abrading.
One object of the present invention is to provide a cooling fluid which will be more eflicient in the cooling operation. Another object of this invention is to accomplish this superior cooling without any attendant sacrifice of lubricating 30,000, 60,000, 80,000, 100,000, etc.
properties or cleansing characteristics, i. e., washing away of metal or abraded particles. By the attainment of these objects, several advantages accrue. by avoiding burns or overheating it is possible to impart a finer finish and truer precision to the metal parts being machined, and by reason of the faster cooling the operation may be considerably accelerated with a resultant increase in production.
Broadly the invention comprises using as a cooling fluid a composition comprising a major proportion of a volatile organic liquid of relatively low viscosity and containing dissolved therein a minor proportion of a viscosity-increasing high molecular weight linear essentially aliphatic polymer which, upon subjection to elevated temperature, is capable of depolymerizing and vaporizing without substantial carbonization or tar formation. Although not essential, it is desirable also to add a minor amount of one or more oiliness or anti-sieze agents.
The volatile organic liquid to be used should be one boiling below about 750 F. and may suit ably be a light petroleum distillate boiling below the lubricating oil boiling range as, for instance, mineral seal oil or kerosene. For instance, it may be a mineral seal oil having a boiling range from about filo-670 F., or 500-700 F., or a kerosene boiling from about 350-500 F., or 355-5l0 F., etc. Instead of using plain hydrocarbon liquid, one may use various oxygenated compounds, halogenated compounds, etc., or derivatives thereof.
The primary object in using the above described types of volatile liquid as the cooling fluid of this invention is to make use of the latent heat of evaporation rapidly to absorb the heat of abrasion. The substance to be used in this capacity should be substantially non-toxic and non-corrosive both in the liquid state and vapor state, for of course during the grinding operations a substantial amount of this volatile liquid is vaporized at the point of grinding.
As the viscosity-increasing polymer it is preferred to use polyisobutylene having an average molecular weight above 800 and preferably about 2000, such as 5,000 or 10,000, although if desired isobutylene polymers having even considerably higher molecular weights may be used, such as In general,
however, polymers having an average molecular weight between-about 2,000 and 15,000 or 20,000 are available at lower cost than the higher molecular weight ones and serve at least as well for the purposes of this invention, or perhaps even better than polymers having molecular weights of 30,000 or above. Other polymerized iso-oleflns having similar characteristics may be used, for instance, polymerized isoamylene, e. g., polymerized methyl 2 butene 1, etc. Qther hydrocarbon polymers which may be used as thickeners include high molecular weight plastic or solid polyethylene, or similar plastic or solid copolymers such as a copolymer of isobutylene and ethylene, made for instance at 100-400" C. under high pressure of 500-2,000 atmospheres with the addition of a small amount of oxygen, or isobutylene-diolefin copolymers ranging, for instance, from 5,000 to 50,000 or more, such as made by copolymerizing a mixture of 90% of isobutylene and 10% butadiene at 103 C. using liquid ethylene as refrigerant and using a solution of aluminum chloride in ethyl chloride as catalyst.
In place of such hydrocarbon polymers, one may use high molecular weight oxygen-containing viscosity-increasing linear aliphatic polymers, preferably having a molecular weight of at least 1,000. One such oxygen-containing thickener is a high molecular weight polymer of an oxygencontaining compound having the group C=CH2 in its molecular structure. Such additives include polymers of vinyl ethers having the general formula:
in which R1 is an unsubstituted or substituted aliphatic, aromatic, or hydroaromatic radical, and R2 is a hydrogen atom or a substituted or unsubstituted aliphatic radical, e, g., vinyl oleyl ether, vinyl isobutenyl ether, vinyl meta-cresyl ether, vinyl cyclohexyl ether, vinyl octadecyl ether, vinyl chloroethyl ether, vinyl amino propyl ether, a-ethylvinyl isohexyl ether, a-chloromethyl vinyl lauryl ether, etc.; polymers of vinyl esters having the general formula in which R1 and R2 are as above and n is an integer having a value of 1 or more, e. g., vinyl stearate, vinyl ester of acids obtained by oxidation of paraifin wax, vinyl chloropropionate, vinyl aminopalmitate, vinyl adipate, vinyl citrate, etc.; polymers of acrylic acid esters having the general formula, ROOCC(X) =CH2, in which R is an unsubstituted or substituted aliphatic, aromatic, or hydroaromatic group, preferably containing at least 10 carbon atoms, and X is a H or a halogen atom, or 2. CH3 group or a C2H5 group, e. g., lauryl acrylate, cetyl acrylate, octadecyl acrylate, amylphenyl methacrylate, isoheptyl cyclohexyl chloroacrylate, chlorodecyl methacrylate, etc., especially such polyacrylic esters having a molecular weight of 5,000 to 10,000.
Another case of high molecular weight, oxygen-containing substances which can be used for the purposes of this invention is the class of condensation products or polyesters of substituted fatty acids having the general formula,
in which R is a H atom or an unsubstituted or substituted aliphatic, aromatic, or hydroaromatic group, :n and 3 may equal or any integer provided that :c+y equals at least 5, and where n is 0 or an integer and m is a whole number and Z is a functional group which has one replaceable hydrogen atom, Z being capable of esterifying a carboxyl group. Some of these polyesters are described in U. S. Patent 2,147,647, and are typified by the polyester having a molecular weight of about 14,000 obtained by polyesterificatlon oi 12-hydroxy stearic acid in the presence of a small amount of adipic acid.
As an oiliness agent or anti-freeze agent, one may use various materials known to the art such as oleic acid, tricresyl phosphate, isopropyl esters of wax oxidation acids and soda.
In carrying out the invention it is desirable to use a sufficient amount of the viscosity-increasing polymer to raise the viscosity of the volatile liquid from a value in the range from about 30 to 50 seconds Saybolt at F. up to a viscosity in the range of about -500 seconds Saybolt at 100 F., preferably about 200-4500 seconds at 100 F. The amount of polymer or thickener required for this purpose will not only depend upon the exact viscosity desired in the finished blend, but will also depend upon the molecular weight of the polymer, as well as the individual thickening ability of the particular polymer used which varies slightly according to the chemical structure of the polymer. As a general guide,' however, the following table is given to show the amount of high molecular weight polyisobutylene required to raise the viscosity of a mineral seal oil up to various values ranging from 150-500 seconds Saybolt at 100 F.; figures are given for two different molecular weights of polymer.
Per Cent Polyisobutylene Viscosity, Sea/100 F.
18,000 60,000 M. W. M. W.
This table shows that about 2.5% of 60,000 molecular weight polyisobutylene will raise the viscosity of mineral seal oil up to 150 seconds Saybolt at 100 F., and that 4.5% of such polymer will raise the viscosity up to about 500 seconds Saybolt, whereas, on the other hand, 6.0 and 10.0% of a lower molecular weight polyisobutylene (having an average molecular weight of about 18,000) will be required similarl to produce a blend having a final viscosity of about 150 seconds and 500 seconds Saybolt at 100 F.
As an example of the thickening ability of the oxygen-containing polymer it may be noted that a lauryl alpha methacrylate polymer having an average molecular weight of about 10,000 will be required in a concentration of about 11% to raise the viscosity of the mineral seal oil to 150 seconds Saybolt at 100 F., but only about 7% will be required of a 16,000 average molecular weight lauryl alpha methacrylate polymer.
It is thus obvious that the amount of polymer to be used will ordinaril range from about 1-20%, generally about 2-15% by weight.
The amount of oiliness agent to be used will depend primarily upon the type of such agent used, but will ordinarily range from about .02 to 10%, preferably about 1-5%. about 3-8% or so of oleic acid may be used,
whereas smaller amounts such as 0.5 to 2% of tricresyl phosphate may be used.
To show the practical application of the invention the following example is submitted:
A blend was prepared having the following composition:
This blend was used as a cooling fluid on a high speed tap grinding machine operating at a spindle speed of 2400 R. P. M. using a Norton abrading wheel 7" x 12" x A", the tap of which had a diameter of 1.25 cm. (less than 0.500 diameter) and was made of special steel having a Rockwell hardness of 064-66, and was provided with a Whitworth full English thread. The oil blend had a viscosity of 202 seconds at 100 F. The room temperature was 72 F. and the temperature of the oil in the machine was 80 F. A thread grinding operation was accomplished in two passes, one a rough pass of 0.030", and one a finished pass of 0.003". After 40 hours of running on such operation, the oil was still light in color, the machine was clean, indicating good cleansing action and scarf deposition in the sump and. not on the machine. Although during similar operations using a conventional cutting oil a steady stream of sparks were obtained, no sparking was obtained with the cooling fluid of this invention. A substantial amount of smoke was formed due to vaporization of the cooling fluid, but this is readily removed by a ventilation hood placed over the machine. The tap turned out by this high speed grinding machine during this test was considerably cleaner than obtained during use of a conventional cutting oil which permitted burns on both sides of the tap.
It is not intended that the invention be limited to any of the materials which have been mentioned merely as specific examples nor by the specific proportions given merely for the sakeof illustration, but it is intended to claim all novelty inherent in the invention, as well as all modifications coming within the scope and spirit of the invention. To the extent that it discloses and claims common subject matter, this application is a continuation-in-part of copendingapplication Serial No. 366,714, filed November 22, 1940, now Patent No. 2,356,367, dated August 22, 1944.
I claim:
1. The method of carrying out high speed grinding operations in which an abrading wheel rotates at high speed against metalstock which comprises applying to the metal at the point of abrasion a viscous lubricant comprising a major portion of a non-toxic, non-corrosive volatile,
liquid, a substantial proportion of which is vaporizable by the heat of abrasion, and a minor portion up to about 20% by weight of an aliphatic polymeric thickener adapted to decompose at elevated temperatures without leaving any substantial residue, said thickener being a high molecular weight viscosity-increasing polymer having an average molecular weight of not less than 800.
2. The method of carrying out high speed grinding operations in which an abrading wheel rotates at high speed against metal stock and generates a large amount of heat which comprises applying to the metal stock at the point of abrasion a viscous lubricant comprising a major portion of a petroleum distillate boiling between about 350 and 750 F. a substantial proportion of which is vaporized by the heat of abrasion and a minor portion of about 1 to 20% by weight of a substantially saturated aliphatic polymer having a molecular weight of at least 1000 dissolved in said distillate to make a solution having a viscosity between about 150 and 500 seconds Saybolt at F.
3. A method according to claim 2 in which the polymer is a polyisobutylene having an average molecular weight within the range of about 5000 to 80,000.
4. The method of carrying out high speed thread grinding operations by grinding a thread in a piece of steel stock by an abrading wheel rotating at high speed, which comprises applying to the steel at the point of abrasion a cooling fiuid consisting essentially of about 92-93% of mineral seal oil, about 2.5% of polyisobutylene having an average molecular weight of about 60,000, and about 5% of oleic acid.
DONALD L WRIGHT.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Great Britain Mar. 11, 1937
US502462A 1943-09-15 1943-09-15 Cooling fluid Expired - Lifetime US2431008A (en)

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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2453710A (en) * 1946-09-17 1948-11-16 Standard Oil Co Grinding oil composition
US2486493A (en) * 1947-01-09 1949-11-01 Tidewater Associated Oil Compa Oil compositions
US2581132A (en) * 1949-07-13 1952-01-01 Texas Co Lubricating oil
US2695877A (en) * 1950-03-01 1954-11-30 Socony Vacuum Oil Co Inc Water-in-oil soluble oil
US2751039A (en) * 1952-12-23 1956-06-19 California Research Corp Filters coated with thickened oils
US2842499A (en) * 1958-07-08 New synthetic lubricants
US2972578A (en) * 1956-01-26 1961-02-21 Sinclair Refining Co Foam inhibited soluble oil composition
US3475442A (en) * 1965-12-08 1969-10-28 North American Rockwell Brazing alloy binder
US4828727A (en) * 1987-10-29 1989-05-09 Birko Corporation Compositions for and methods of lubricating carcass conveyor
EP0690121A3 (en) * 1994-06-27 1996-07-31 Carrier Corp Metal forming lubricant
US6207286B1 (en) 1997-04-18 2001-03-27 Alcoa Inc. Lubricated sheet product and lubricant composition

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US1319129A (en) * 1919-10-21 Henry matthew wells
GB399527A (en) * 1928-05-10 1933-10-04 Ig Farbenindustrie Ag A process for improving oils, especially lubricating oils
US2020703A (en) * 1932-10-11 1935-11-12 Ig Farbenindustrie Ag Improved hydrocarbon products, especially lubricating oils
US2020714A (en) * 1932-10-12 1935-11-12 Ig Farbenindustrie Ag Lubricating hydrocarbon product
GB462556A (en) * 1934-10-02 1937-03-11 Celluloid Corp Improvements in lubricating compositions
GB467932A (en) * 1935-03-29 1937-06-25 Standard Oil Dev Co Improvements relating to polymers of isobutylene
US2097468A (en) * 1932-01-30 1937-11-02 Ig Farbenindustrie Ag Production of hydrocarbons of high molecular weight
US2177316A (en) * 1936-04-11 1939-10-24 American Sheet & Tin Plate Grinding
US2228429A (en) * 1938-09-20 1941-01-14 Standard Oil Dev Co Pneumatic tool lubricant
US2233436A (en) * 1940-01-22 1941-03-04 Lubri Zol Dev Corp Lubricant
US2334996A (en) * 1939-08-18 1943-11-23 Jasco Inc Thickened oil composition
US2356367A (en) * 1940-11-22 1944-08-22 Jasco Inc High temperature lubricant

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1319129A (en) * 1919-10-21 Henry matthew wells
GB399527A (en) * 1928-05-10 1933-10-04 Ig Farbenindustrie Ag A process for improving oils, especially lubricating oils
US2097468A (en) * 1932-01-30 1937-11-02 Ig Farbenindustrie Ag Production of hydrocarbons of high molecular weight
US2020703A (en) * 1932-10-11 1935-11-12 Ig Farbenindustrie Ag Improved hydrocarbon products, especially lubricating oils
US2020714A (en) * 1932-10-12 1935-11-12 Ig Farbenindustrie Ag Lubricating hydrocarbon product
GB462556A (en) * 1934-10-02 1937-03-11 Celluloid Corp Improvements in lubricating compositions
GB467932A (en) * 1935-03-29 1937-06-25 Standard Oil Dev Co Improvements relating to polymers of isobutylene
US2177316A (en) * 1936-04-11 1939-10-24 American Sheet & Tin Plate Grinding
US2228429A (en) * 1938-09-20 1941-01-14 Standard Oil Dev Co Pneumatic tool lubricant
US2334996A (en) * 1939-08-18 1943-11-23 Jasco Inc Thickened oil composition
US2233436A (en) * 1940-01-22 1941-03-04 Lubri Zol Dev Corp Lubricant
US2356367A (en) * 1940-11-22 1944-08-22 Jasco Inc High temperature lubricant

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2842499A (en) * 1958-07-08 New synthetic lubricants
US2453710A (en) * 1946-09-17 1948-11-16 Standard Oil Co Grinding oil composition
US2486493A (en) * 1947-01-09 1949-11-01 Tidewater Associated Oil Compa Oil compositions
US2581132A (en) * 1949-07-13 1952-01-01 Texas Co Lubricating oil
US2695877A (en) * 1950-03-01 1954-11-30 Socony Vacuum Oil Co Inc Water-in-oil soluble oil
US2751039A (en) * 1952-12-23 1956-06-19 California Research Corp Filters coated with thickened oils
US2972578A (en) * 1956-01-26 1961-02-21 Sinclair Refining Co Foam inhibited soluble oil composition
US3475442A (en) * 1965-12-08 1969-10-28 North American Rockwell Brazing alloy binder
US4828727A (en) * 1987-10-29 1989-05-09 Birko Corporation Compositions for and methods of lubricating carcass conveyor
EP0690121A3 (en) * 1994-06-27 1996-07-31 Carrier Corp Metal forming lubricant
US6207286B1 (en) 1997-04-18 2001-03-27 Alcoa Inc. Lubricated sheet product and lubricant composition

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