US2852470A - Refrigeration composition - Google Patents

Refrigeration composition Download PDF

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US2852470A
US2852470A US462586A US46258654A US2852470A US 2852470 A US2852470 A US 2852470A US 462586 A US462586 A US 462586A US 46258654 A US46258654 A US 46258654A US 2852470 A US2852470 A US 2852470A
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hindered
ester
acid
refrigerant
lubricant
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US462586A
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Albert L Henne
Victor A Williamitis
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Motors Liquidation Co
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Motors Liquidation Co
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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
    • C10M171/008—Lubricant compositions compatible with refrigerants
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/02—Materials undergoing a change of physical state when used
    • C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
    • C09K5/041—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
    • C09K5/044—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds

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  • An object of this invention is to provide a working fluid consisting of a refrigerantand a lubricant miscible in the refrigerant, the lubricant being an ester (the-word ester is used in the specification and claimsto include a single ester or a polyester) which is hindered and which does not react with water and, otherattacking ,agents generally present in refrigerating apparatus to produce acids or other compounds harmful to the operation of the apparatus.
  • Another object of this invention is to provide a refrigerating apparatus in which the motor statoris insulated with an ester which is hindered and does not react with water or other attacking agents generally present in refrigerating apparatus to produce acids or other .compounds harmful to the operation of the apparatus,- and which hindered ester is insoluble in the refrigerant and/ or lubricant being used in the refrigerating apparatus.
  • Another object of this invention isto providefirlthe same refrigerating apparatus a lubricanthand.
  • a'stator insulating material each of a hindered ester ofthecharacter described in the foregoing objects, wherein preferably the ester as a lubricant is hindered to increase its chemical strength.
  • the hindered'esters-used as lubricants are miscible in the refrigerant whereas the hindered esters used as insulatory materials are not soluble in the refrigerant and/ or the lubricant.
  • Figure 1 is a diagrammatic representation of a'refrigerating apparatus embodying this invention.
  • FIGS 2 through 13 are chemical formulae used in the explanation of the chemical principles involved'in-the manufacture and use of the hindered esters embodying this invention.
  • a refrigerating apparatus embodying this invention is diagrammatically indicated in Figure l.
  • a motor compressor unit it discharges compressed refrigerant, carrying some lubricant, through a pipe 11, to a condenser 12, from whence condensed refrigerant and lubricant pass to an expanding device such as a capillary tube 13, and from thence to an evaporator 14 from whence theevaporated refrigerant with the lubricant flows through the pipe 15 to the compressor 16.
  • the compressor 16 discharges the compressed refrigerant mixture into the dome 17 from whence the compressed mixture flows again through irthe refrigerating apparatus.
  • the compressor 16 is driven .byamotor rotor 19 energized by a stator 20.
  • a body of lubricating-liquid 21 is maintained in the motor compressor 20 for lubrication of the moving parts and in -which-lubricant of the character described in this application is concentrated by the heat of the compressor and motor.
  • the stator 20 has electric windings, which are .protected by an insulator, applied as wire coatings to litheiwindings individually or applied as stator slot insu latorsand coil separators .to the stator as a whole; such insulation is diagrammatically indicated at 22.
  • the lubricant is soluble in the refrigerant, whereas the insulator 22 is insoluble in the refrigerant and remains in the solid, or nearly solid, phase at all operating temperatures of the apparatus.
  • the refrigerant exists in the liquid and gaseous phase at the operating temperatures of the apparatus, and preferably-comprises a fluoro halo derivative of an aliphatic hydrocarbon of the character disclosed in the patent to M-idgley et al., Re. 19,265, reissued August 7, 1934.
  • This patent discloses the various compounds which can be derived from CH or CH CH F by chlorine and/or fluorine and/or bromine substitution.
  • the preferred compounds include fluorochloro derivatives of methane .and .ethane such as CF C1 CHFCl C F Cl and C F Cl .Estershave been used heretofore as lubricants in various rnachines. However, such esters have been unhindered as to water, and other attacking agents, and
  • any of a group of hindered esters may be used as a lubricant and/or as a stator -insulator, which esters. have a one-way, or unreversible, equation with respect to water, and. similar attacking agents, so that such esterscannot be changed to acids or similarly harmful compounds.
  • the forming acid is also hindered .by thesame radicals but can be caused. to react withan alcohol in the presence of concentrated sulphuric acid, for example (outside the refrigerating apparatus), to produce the hindered ester, which, once formed, cannot return to the acid state in the refrigerating apparatus in the presence of water or the like.
  • the obstacle producers generally indicated by the character A in this application, and which produce the hindered compounds referred to in this application, may
  • alkyl radicals such as CH CnH or may be suitable aryl radicals, or a halogen radical such as Cl.
  • the A obstacle in open attached on the carbon adjacent to the C 11 of the hindered acid from which the hindered ester is derived.
  • the obstacles are on the adjacent C, but in Figure 5 which refers to benzene derivatives, there must be two carbons removed from the acid group.
  • two such obstacles should be attached to block any access to the molecule by water or other attacking agent.
  • FIG. 5 A special case, for illustration only, of such properly hindered benzene type acid capable of forming the hindered ester is indicated in Figure 5, wherein the obstacle producers A are either CH CnH or Cl, or similar radicals above referred to and in which the figure illustrates a representative hindered acid of the benzene group, which acid is used in forming a representative hindered ester for use according to this invention.
  • the obstacle producers A are either CH CnH or Cl, or similar radicals above referred to and in which the figure illustrates a representative hindered acid of the benzene group, which acid is used in forming a representative hindered ester for use according to this invention.
  • a hindered ester of the benzene type may be made from a hindered acid and an alcohol in the presence of concentrated sulphuric acid, for example, as indicated in Figure 6.
  • any hindered acid, benzene type or otherwise, as illustratively indicated in Figure 5 is brought into contact with any alcohol, illustratively indicated as HOR, in the presence of concentrated sulphuric acid, outside the refrigerating apparatus, produces a hindered ester and water.
  • Figure 6 indicates any of the hindered esters which may be used as lubricants or as stator insulators in the refrigerating apparatus indicated in Figure 1.
  • Such hindered esters, in the presence of water or similar attacking agent cannot react in the refrigerating apparatus to return to the acid condition or to form any similarly undesirable compound.
  • the hindered ester is at present preferred to be a large molecule ester, i. e., a hindered ester of a large acid, formed with a large alcohol, or else a hindered polyester of a hindered polyaeid formed with polyalcohol (for instance ethylene glycol).
  • a large molecule hindered ester i. e., a hindered ester of a large acid, formed with a large alcohol
  • a hindered polyester of a hindered polyaeid formed with polyalcohol for instance ethylene glycol.
  • polyalcohol for instance ethylene glycol
  • Hindered polyesters of the general type disclosed in Figure 7 may be used either as lubricants or as stator insulators, depending on the melting temperature.
  • those polyesters in which n (n indicates the number of benzene or alkyl groups or radicals) is small have relatively low melting temperatures, and are suitable as lubricants, whereas those in which "12 is relatively large have relatively high melting temperatures, and are suitableas stator insulators.
  • the character of the A obstacle producers also has an influence on the melting temperature.
  • a hindered polyester is preferred in sufiicient molecular size to be a solid under all operating tempera- Y tures of the apparatus.
  • the hindering groups A preferably are CH or CnH rather than C1 or halogen for the purpose of eliminating solubility in the refrigerants being used.
  • Figures 8, 9 indicate specific examples of a large group of hindered esters which may be used as lubricants in refrigerating apparatus .or the like.
  • Figure 8 indicates the formula for di-Z-ethylhexyla-A-tetrachloro-adipate. Methyl or ethyl groups (or similar) could be used instead of the chlorine.
  • Figure 9 indicates the (formula for di-Z-ethylhexyl- 3-6-dichloro-orthophthalate.
  • Figure 10 indicates the formula for di-Z-ethylhexyl- 2,3,5,6-tetrachloro-terephthalate.
  • Figures 11, 12 and 13 indicate specific examples of a large group of hindered esters which may be used as insulators for stators in refrigerating apparatus or the like.
  • Figure 11 indicates the formula for polyester of tetrachloro-terephthalic acid and ethylene glycol.
  • Figure 12 indicates the formula for polyester of tetrachloro-terephthalic acid and tetra-methylene glycol.
  • Figure 13 indicates the formula for polyester of tetrachloro-terephthalic acid and decamethylene glycol.
  • a hindered ester of the type soluble in the refrigerant may be used as a lubricant in the same apparatus in which another hindered ester, insoluble in the refrigerant and the lubricant, is used as a motor stator insulator.
  • the soluble hindered ester circulates with the refrigerant throughout the system for lubricating purposes, whereas the insoluble hindered ester remains on the motor stator and protects the windings, because it remains solid under all normal operating temperatures of the apparatus, and is insoluble in the refrigerant, and in the lubricant.
  • a refrigerant which is a fiuorochloro derivative of a class of aliphatic compounds selected from the group consisting of methane and ethane capable of being in the liquid and gaseous phases within the operating temperatures of said refrigerating apparatus, and a lubricant comprising a fully esterfied reaction product of di-Z-ethylhexyl alcohol and a polybasic acid selected from the group con sisting of a-A-tetrachloro-adipic acid, 3-6-dichloroorthophthalic acid and 2,3,5,6-tetrachloro-terephthalic acid.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Physics & Mathematics (AREA)
  • Combustion & Propulsion (AREA)
  • Thermal Sciences (AREA)
  • Materials Engineering (AREA)
  • Lubricants (AREA)
  • Organic Insulating Materials (AREA)

Description

2,852,470 REFRIGERATION coMrosrnoN Application October 15, 1954, Serial 'No. 462,586 1 Claim. ((1252- 68) States Pat enc -O f Patented Sept. 16, 1958 ice "::the pipe 11 .to the condenser 12 for recirculation through This invention relates to refrigerating apparatus and particularly to refrigerating apparatus of the compression type wherein the non-metallic parts thereof, such as the lubricant and the motor stator insulation normally coming in direct contact with the refrigerant, are selected from the chemical group generally .called .hindered esters or esters which, under the conditions encountered in a refrigerating system, do not react in a reversible manner to produce the acids and the alcohols from which they were formed.
An object of this invention is to provide a working fluid consisting of a refrigerantand a lubricant miscible in the refrigerant, the lubricant being an ester (the-word ester is used in the specification and claimsto include a single ester or a polyester) which is hindered and which does not react with water and, otherattacking ,agents generally present in refrigerating apparatus to produce acids or other compounds harmful to the operation of the apparatus.
Another object of this invention is to provide a refrigerating apparatus in which the motor statoris insulated with an ester which is hindered and does not react with water or other attacking agents generally present in refrigerating apparatus to produce acids or other .compounds harmful to the operation of the apparatus,- and which hindered ester is insoluble in the refrigerant and/ or lubricant being used in the refrigerating apparatus.
Another object of this invention isto providefirlthe same refrigerating apparatus a lubricanthand. a'stator insulating material, each of a hindered ester ofthecharacter described in the foregoing objects, wherein preferably the ester as a lubricant is hindered to increase its chemical strength. The hindered'esters-used as lubricants are miscible in the refrigerant whereas the hindered esters used as insulatory materials are not soluble in the refrigerant and/ or the lubricant.
Further objects and advantages of" the present invention will be apparent from the following" description, reference being had to the accompanying drawings wherein a preferred form of the invention is clearly shown.
In the drawings:
Figure 1 is a diagrammatic representation of a'refrigerating apparatus embodying this invention.
Figures 2 through 13 are chemical formulae used in the explanation of the chemical principles involved'in-the manufacture and use of the hindered esters embodying this invention.
A refrigerating apparatus embodying this invention is diagrammatically indicated in Figure l. A motor compressor unit it discharges compressed refrigerant, carrying some lubricant, through a pipe 11, to a condenser 12, from whence condensed refrigerant and lubricant pass to an expanding device such as a capillary tube 13, and from thence to an evaporator 14 from whence theevaporated refrigerant with the lubricant flows through the pipe 15 to the compressor 16. The compressor 16 discharges the compressed refrigerant mixture into the dome 17 from whence the compressed mixture flows again through irthe refrigerating apparatus. The compressor 16 is driven .byamotor rotor 19 energized by a stator 20. A body of lubricating-liquid 21 is maintained in the motor compressor 20 for lubrication of the moving parts and in -which-lubricant of the character described in this application is concentrated by the heat of the compressor and motor. The stator 20 has electric windings, which are .protected by an insulator, applied as wire coatings to litheiwindings individually or applied as stator slot insu latorsand coil separators .to the stator as a whole; such insulation is diagrammatically indicated at 22. The lubricant is soluble in the refrigerant, whereas the insulator 22 is insoluble in the refrigerant and remains in the solid, or nearly solid, phase at all operating temperatures of the apparatus.
The refrigerant exists in the liquid and gaseous phase at the operating temperatures of the apparatus, and preferably-comprises a fluoro halo derivative of an aliphatic hydrocarbon of the character disclosed in the patent to M-idgley et al., Re. 19,265, reissued August 7, 1934. This patent discloses the various compounds which can be derived from CH or CH CH F by chlorine and/or fluorine and/or bromine substitution. The preferred compounds include fluorochloro derivatives of methane .and .ethane such as CF C1 CHFCl C F Cl and C F Cl .Estershave been used heretofore as lubricants in various rnachines. However, such esters have been unhindered as to water, and other attacking agents, and
. react with water or such agents to produce the original acids and alcohols and other compounds which are harmful to theroperation of-the mechanism being lubricated. Hence such-esters are particularly unsatisfactory 'inrefrigerating apparatus. The two-way, or reversible, character .of the equation between an unhindered ester and water (as an example ofan attacking agent) which could harmfullytake place in a refrigerating apparatus, is indicated in Figure 2.
According to this invention, any of a group of hindered esters may be used as a lubricant and/or as a stator -insulator, which esters. have a one-way, or unreversible, equation with respect to water, and. similar attacking agents, so that such esterscannot be changed to acids or similarly harmful compounds.
The oneway, unreversible character of .an equation of a hinderedester, according to this invention, with water (asillustra-tive of an attacking agent) is indicated in Figure 3. .This indicates that a hindered ester in there- .frigera'ting apparatus cannot react with water to form an acid, even if the ester can be produced outside therefrigera'ting apparatus from a hindered acid withthe formation of vwater.
A general equation to form such a hindered ester,.and j'of itsunreversible equation with an alcohol on one side of the equation and with water on the other side is indicated in Figure 4. The hindrance is here pictured by obsta'cles, denoted as A in this and other figires in this application to indicate radicalswhich render. the
0 .hindered esternon-reactant to water or the like in the refrigerating apparatus. The forming acid is also hindered .by thesame radicals but can be caused. to react withan alcohol in the presence of concentrated sulphuric acid, for example (outside the refrigerating apparatus), to produce the hindered ester, which, once formed, cannot return to the acid state in the refrigerating apparatus in the presence of water or the like.
The obstacle producers, generally indicated by the character A in this application, and which produce the hindered compounds referred to in this application, may
be alkyl radicals, such as CH CnH or may be suitable aryl radicals, or a halogen radical such as Cl.
. 3 The A obstacle, in open attached on the carbon adjacent to the C 11 of the hindered acid from which the hindered ester is derived. In Figure 4, which refers to open chain compounds, the obstacles are on the adjacent C, but in Figure 5 which refers to benzene derivatives, there must be two carbons removed from the acid group. Preferably, two such obstacles should be attached to block any access to the molecule by water or other attacking agent. A special case, for illustration only, of such properly hindered benzene type acid capable of forming the hindered ester is indicated in Figure 5, wherein the obstacle producers A are either CH CnH or Cl, or similar radicals above referred to and in which the figure illustrates a representative hindered acid of the benzene group, which acid is used in forming a representative hindered ester for use according to this invention.
A hindered ester of the benzene type may be made from a hindered acid and an alcohol in the presence of concentrated sulphuric acid, for example, as indicated in Figure 6. In Figure 6, any hindered acid, benzene type or otherwise, as illustratively indicated in Figure 5, is brought into contact with any alcohol, illustratively indicated as HOR, in the presence of concentrated sulphuric acid, outside the refrigerating apparatus, produces a hindered ester and water. Thus Figure 6 indicates any of the hindered esters which may be used as lubricants or as stator insulators in the refrigerating apparatus indicated in Figure 1. Such hindered esters, in the presence of water or similar attacking agent, cannot react in the refrigerating apparatus to return to the acid condition or to form any similarly undesirable compound.
For practical purposes, the hindered ester is at present preferred to be a large molecule ester, i. e., a hindered ester of a large acid, formed with a large alcohol, or else a hindered polyester of a hindered polyaeid formed with polyalcohol (for instance ethylene glycol). Such large molecule hindered ester, and its formation, is indicated, by way of example, in Figure 7, in which the acid is a hindered polyaeid of the benzene type, and in which any alcohol or any polyalcohol, such as ethylene glycol, may be used in the presence of concentrated sulphuric acid to produce a hindered polyester and water.
Hindered polyesters of the general type disclosed in Figure 7 may be used either as lubricants or as stator insulators, depending on the melting temperature. In general, those polyesters in which n (n indicates the number of benzene or alkyl groups or radicals) is small have relatively low melting temperatures, and are suitable as lubricants, whereas those in which "12 is relatively large have relatively high melting temperatures, and are suitableas stator insulators. The character of the A obstacle producers also has an influence on the melting temperature.
In the application of a hindered ester to electrical insulation, a hindered polyester is preferred in sufiicient molecular size to be a solid under all operating tempera- Y tures of the apparatus. The hindering groups A preferably are CH or CnH rather than C1 or halogen for the purpose of eliminating solubility in the refrigerants being used.
Figures 8, 9 and indicate specific examples of a large group of hindered esters which may be used as lubricants in refrigerating apparatus .or the like.
chain compounds, should be Figure 8 indicates the formula for di-Z-ethylhexyla-A-tetrachloro-adipate. Methyl or ethyl groups (or similar) could be used instead of the chlorine.
Figure 9 indicates the (formula for di-Z-ethylhexyl- 3-6-dichloro-orthophthalate.
Figure 10 indicates the formula for di-Z-ethylhexyl- 2,3,5,6-tetrachloro-terephthalate.
Figures 11, 12 and 13 indicate specific examples of a large group of hindered esters which may be used as insulators for stators in refrigerating apparatus or the like.
Figure 11 indicates the formula for polyester of tetrachloro-terephthalic acid and ethylene glycol.
Figure 12 indicates the formula for polyester of tetrachloro-terephthalic acid and tetra-methylene glycol.
Figure 13 indicates the formula for polyester of tetrachloro-terephthalic acid and decamethylene glycol.
In Figures ll, 12 and 13 n is to be high enough to give molecular weights of 15,000 or higher.
A hindered ester of the type soluble in the refrigerant may be used as a lubricant in the same apparatus in which another hindered ester, insoluble in the refrigerant and the lubricant, is used as a motor stator insulator. In this case, the soluble hindered ester circulates with the refrigerant throughout the system for lubricating purposes, whereas the insoluble hindered ester remains on the motor stator and protects the windings, because it remains solid under all normal operating temperatures of the apparatus, and is insoluble in the refrigerant, and in the lubricant. While the form of embodiment of the invention as herein disclosed constitutes a preferred form, it is to be understood that other forms might be adopted as may come within the scope of the claim which follows.
What is claimed is as follows:
As a working fiuid for a refrigeration apparatus of the seal compressor of the compression type, a refrigerant which is a fiuorochloro derivative of a class of aliphatic compounds selected from the group consisting of methane and ethane capable of being in the liquid and gaseous phases within the operating temperatures of said refrigerating apparatus, and a lubricant comprising a fully esterfied reaction product of di-Z-ethylhexyl alcohol and a polybasic acid selected from the group con sisting of a-A-tetrachloro-adipic acid, 3-6-dichloroorthophthalic acid and 2,3,5,6-tetrachloro-terephthalic acid.
References Cited in the file of this patent UNITED STATES PATENTS 1,719,807 Kucher July 2, 1929 1,886,034 Macallum Nov. 1, 1932 1,950,468 Zwilgmeyer Mar. 13, 1934 1,955,345 Sarnmark Apr. 17, 1934 2,006,411 Rosenstein July 2, 1935 2,040,902 Zellhoefer May 19, 1936 2,169,097 Hall et al. Aug. 8, 1939 2,187,388 Williams Ian. 16, 1940 2,199,415 Philipp May 7, 1940 2,307,588 Jackson et a1 Jan. 5, 1943 2,324,739 Stoops July 20, 1943 2,455,873 Norlander et a1 Dec. 7, 1948 2,542,785 Walker Feb. 20, 1951 2,548,493 Robey Apr. 10, 1951
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Cited By (22)

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US3112356A (en) * 1961-04-28 1963-11-26 Du Pont Benzoic acid ester dielectric compositions and electrical apparatus in combination therewith
US3135885A (en) * 1959-03-26 1964-06-02 Smith Corp A O Dynamoelectric machines
US3209992A (en) * 1963-02-21 1965-10-05 Danfoss Ved Ing M Clausen Hermetically enclosed small refrigerating machine and procedure for the operation ofsaid machine
US3210404A (en) * 1962-07-16 1965-10-05 Continental Oil Co Di-neoalkyl beta, beta, beta1, beta1-tetraloweralkyl-substituted alkylene dicarboxylates
US3214461A (en) * 1962-02-26 1965-10-26 Eastman Kodak Co Preparation of 2, 2, 4, 4-tetraalkyl-3-oxobutyric acid esters from 2, 2, 4, 4-tetraalkylcyclo-butane-1, 3-dione
US3261862A (en) * 1962-09-24 1966-07-19 Exxon Research Engineering Co Esterification of sterically hindered alkanoic acids in the presence of stoichiometric amounts of a boron fluoride compound
US3271315A (en) * 1963-11-01 1966-09-06 Continental Oil Co Use of hindered esters of carboxylic acids as radiation resistant lubricants
US3766416A (en) * 1971-05-15 1973-10-16 Papst Motoren Kg Internally insulated, metal enclosed electric motor
US3878112A (en) * 1974-05-23 1975-04-15 Westinghouse Electric Corp Lubricant-refrigerant system for centrifugal refrigeration compressors
US5021179A (en) * 1990-07-12 1991-06-04 Henkel Corporation Lubrication for refrigerant heat transfer fluids
EP0461435A1 (en) * 1990-06-09 1991-12-18 Hoechst Aktiengesellschaft Application of aromatic carboxylic esters as lubricant in refrigerant compressors
EP0496937A1 (en) * 1991-01-30 1992-08-05 Hitachi, Ltd. Lubricant for refrigeration compressors
EP0688855A1 (en) * 1990-11-16 1995-12-27 Hitachi, Ltd. Refrigerating apparatus and refrigerant compressor
US5486302A (en) * 1991-01-17 1996-01-23 Cpi Engineering Services, Inc. Lubricant composition for fluorinated refrigerants used in compression refrigeration systems
US5820777A (en) * 1993-03-10 1998-10-13 Henkel Corporation Blended polyol ester lubricants for refrigerant heat transfer fluids
US5851968A (en) * 1994-05-23 1998-12-22 Henkel Corporation Increasing the electrical resistivity of ester lubricants, especially for use with hydrofluorocarbon refrigerants
US5906769A (en) * 1992-06-03 1999-05-25 Henkel Corporation Polyol ester lubricants for refrigerating compressors operating at high temperatures
US5976399A (en) * 1992-06-03 1999-11-02 Henkel Corporation Blended polyol ester lubricants for refrigerant heat transfer fluids
US6183662B1 (en) 1992-06-03 2001-02-06 Henkel Corporation Polyol ester lubricants, especially those compatible with mineral oils, for refrigerating compressors operating at high temperatures
US6221272B1 (en) 1992-06-03 2001-04-24 Henkel Corporation Polyol ester lubricants for hermetically sealed refrigerating compressors
CN1083538C (en) * 1991-04-30 2002-04-24 株式会社日立制作所 Lubricant for refrigeration compressors
US7018558B2 (en) 1999-06-09 2006-03-28 Cognis Corporation Method of improving performance of refrigerant systems

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US1886034A (en) * 1931-09-04 1932-11-01 Roessler & Hasslacher Chemical Odorant for refrigeration
US1950468A (en) * 1930-04-18 1934-03-13 Nat Aniline & Chem Co Inc Alkyd resinous composition
US1955345A (en) * 1930-05-13 1934-04-17 Sarnmark Axel Uno Absorption refrigerating machine
US2006411A (en) * 1933-07-31 1935-07-02 Shell Dev Process for heat transmission
US2040902A (en) * 1935-04-18 1936-05-19 Glenn F Zellhoefer Absorption refrigeration
US2169097A (en) * 1938-09-01 1939-08-08 Gen Electric Dynamo-electric machine
US2187388A (en) * 1935-09-06 1940-01-16 Gen Motors Corp Working fluid for refrigerating apparatus
US2199415A (en) * 1936-10-17 1940-05-07 Nash Kelvinator Corp Refrigerating apparatus
US2307588A (en) * 1938-07-08 1943-01-05 Gen Electric Insulated electrical conductor
US2324739A (en) * 1939-09-22 1943-07-20 Carbide & Carbon Chem Corp Enamel coating
US2455873A (en) * 1945-07-04 1948-12-07 Gen Electric Modified wax-compatible ethylene glycol-tetrachlorophthalate resins
US2542785A (en) * 1947-12-29 1951-02-20 Du Pont Hydraulic fluids
US2548493A (en) * 1948-08-03 1951-04-10 Standard Oil Dev Co Esters of trimethyladipic acid

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US1719807A (en) * 1923-06-04 1929-07-02 Westinghouse Electric & Mfg Co Refrigerator
US1950468A (en) * 1930-04-18 1934-03-13 Nat Aniline & Chem Co Inc Alkyd resinous composition
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