US2807155A - Working fluids in refrigeration apparatus - Google Patents

Working fluids in refrigeration apparatus Download PDF

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US2807155A
US2807155A US563038A US56303856A US2807155A US 2807155 A US2807155 A US 2807155A US 563038 A US563038 A US 563038A US 56303856 A US56303856 A US 56303856A US 2807155 A US2807155 A US 2807155A
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refrigerant
lubricant
refrigeration apparatus
group
compressor
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Victor A Williamitis
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Motors Liquidation Co
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Motors Liquidation 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
    • C10M171/00Lubricating 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
    • C10M171/008Lubricant compositions compatible with refrigerants
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-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
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/04Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
    • C09K5/041Materials 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
    • C09K5/044Materials 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
    • 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
    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/38Esters of polyhydroxy compounds

Definitions

  • FIG. 1 is a diagrammatic representation of one type of refrigeration apparatus embodying this invention.
  • Figure 2 is a graph comparing Floc points or phase separation of various refrigeration lubricants and a'pentaerythritol ester at various concentrations in Freon 22.
  • a refrigeration apparatus embodying this invention is diagrammatically indicated in Figure l.
  • Amotor. compressor unit 10 discharges compressed refrigerant, carrying some lubricant, through a pipe 12, to a condenser 14. The condensed refrigerant and lubricant then passes to an expansion device such as a capillary tube 16 and then to an evaporator 18. The vaporized mixture of refrigerant and lubricant flow through suction line 20 to the compressor 22 of the motor compressor .unit 10 wherein the vapor is compressed and discharged into dome 24 of the motor compressor unit. The compressed United States Patent O ice vapor is then discharged through pipe 12 for recirculation through the refrigeration apparatus.
  • the compressor 22 is driven by an electric motor comprising a rotor 26 operatively connected to the compressor 22 by shaft 27 and a stator 28 secured to the containing 'member 30 of the motor compressor unit.
  • the compressor 22 is preferably partially submerged in a body of lubricant 32 held in containing member 30 for lubricating the moving parts of the compressor.
  • circulating refrigerant comes in direct contact with the lubricant in the motor compressor unit and carries small amounts of lubricant therewith throughout the refrigeration cycle.
  • the temperature in the refrigeration apparatus may vary from about 100 F. at the end of the capillary tube or expansion device to about 400 F. at the compressor outlet.
  • the refrigeration apparatus described is of the high side type, i. e., the refrigerant enters containing member 30 directly at the compressor so that the fluid in dome 24 is under considerable pressure, it will be obvious that the present invention is also applicable to low side or other types of refrigeration apparatus.
  • the refrigerant used in the present invention preferably comprises a fluoro halo derivative of an aliphatic hydrocarbon of the character disclosed in the patent to Midgeley et al., -Re. 19,265, reissued August 7, 1934, as, for example, trichlorofluoromethane (Freon 11), dichlorodifluoromethane (Freon 12) and particularly difluoromonochloromethane (Freon 22).
  • a fluoro halo derivative of an aliphatic hydrocarbon of the character disclosed in the patent to Midgeley et al., -Re. 19,265, reissued August 7, 1934 as, for example, trichlorofluoromethane (Freon 11), dichlorodifluoromethane (Freon 12) and particularly difluoromonochloromethane (Freon 22).
  • a satisfactory refrigeration lubricant which may be mixed with a refrigerant to constitute a working fluid in a refrigeration apparatus of the type described, is that the lubricant be completely soluble in the particular refrigerant used throughout the range of operating temperatures, and that the lubricant be substantially free of wax, so as to prevent the precipitation of wax or. like substances with consequent blocking or restricting of the capillary tube and/or expansion valves at the low temperatures attained therein.
  • a refrigerant lubricant have high chemical and thermal stability in the presence of the refrigerant used, the metals, motor insulation winding and other materialswith which the lubricant comes into contact and is sealed.
  • the lubricant of the present invention may include esterified monomolecular pentaerythritol described by the following structural formula:
  • R represents a saturated aliphatic straight or--branched-hydrocarbon chain such as "alkyl radicals, and alkyl radicals having substituted aromatic radicals, aromatic groups such as aryl radicals and aryl radicals I v y having substituted aliphatic radicals, the R groups having carbon atoms in the range of about 2 to 20 and preferably an average of from 6 to 10.
  • alkyl as hereinafter used includes both unsubstituted and aromatic radical substituted alkyl radicals and the trmaryl includes both unsubstituted and alkyl radical substituted aryl radicals.
  • the lubricant may also consist of or include the esterified polyethers diapentaerythritol and tripentaerythritol generally described by the following structural formulas:
  • the pentaerythritol compounds may be produced by reacting acetaldehyde with formaldehyde in an alkaline medium under rigorously controlled conditions as is well described in chemical literature.
  • the esters of the present invention may be formed by reacting the pentaerythritol compounds with organic acids having the desired hydrocarbon structures.
  • acids such as n-butyric, n-valeric and caprylic may be used to produce straight chained aliphatic R groups and acids such as isobutyric acid may be used to produce branched chain R groups.
  • aromatic asids such as benzoic acid and paratoluic acid may be used to produce aryl R groups and acids such as phenylacetic acid may be used to produce aromatic radical substituted alkyl R groups.
  • the acids used to produce the present esters are those having no reactive groups other than the carboxyl and preferably those having a single carboxyl group.
  • the R groups mentioned in each molecule of the above-mentioned formulas may each be a different radical selected from the classes of radicals above described and are preferably varied.
  • the lubricant preferably contains a mixture of different esters of the type described above selected so as to have a viscosity range from 50 to 2000 seconds Saybolt (SUS) measured as 100 F., the exact viscosity being dependent on the operating characteristics and the particular refrigerant of the refrigeration apparatus.
  • SUS Saybolt
  • the compounds are preferably fully esterified.
  • the superiority of the present lubricant for refrigeration systems of the type described may be demonstrated by comparing the lubricant with conventionally used refrigeration mineral oil lubricants.
  • the solubility of refrigeration lubricants is generally measured by mixing various percentages of the oil and a refrigerant in a glass pressure apparatus and externally cooling the same until phase separation or Floc point is noted.
  • the graph of Figure 2 shows the temperature of the phase separation plotted against various concentrations of the oil and Freon 22 for lubricants of various viscosities.
  • the refrigerant used in the comparison is Freon 22 since solution of the oil in this refrigerant is more diflicult than in other refrigerants.
  • the oil designated as A is a commercial refrigerant type naphthenic oil having the following specifications:
  • the oil designated as B is a commercial refrigerant type naphthenic oil having the following specifications:
  • the Floc point of both oils A and B having a viscosity of 500 SUS at F. is at 84 F. at a concentration of 20% in Freon 22.
  • the Floc point of oils A and B having a viscosity of SUS at 100 F. are at 46 F. and 34 F., respectively, at a concentration of 20% in Freon 22.
  • the ;-Floc point of a mono pentaerythritol ester having a viscosity of 274 SUS at 100 F. and an average of about 7 aliphatic carbon atoms in the acid portion of the ester groups is -63 F. at a concentration of 20% in Freon 22.
  • the pentaerythritol esters of the present invention exhibit a high degree of thermal and chemical stability.
  • the above A and B oils of comparable viscosity were compared by sealing the lubricant, Freon 22 and metal catalysts in pressurized glass tubes and exposing the combination to high temperatures the results of which are shown below..
  • a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow relationship, a difluoromonochloromethane refrigerant and a lubricant soluble in said refrigerant comprising an organic ester of pentaerythritol which is a reaction product of monopentaerythritol and an organic acid selected from the group wherein the carboxyl group is attached to a radical taken from a group consisting of alkyl and aryl radicals having an average of from 6 to 10 carbon atoms.
  • a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow relationship, a difluoromonochloromethane refrigerant and a lubricant soluble in said refrigerant comprising an organic acid ester which is a reaction product of a pentaerythritol selected from the group consisting of monopentaerythritol, dipentaerythritol and tripentaerythritol, and an organic acid selected from a group wherein the carboXyl group is attached to a radical taken from the group consisting of alkyl and aryl radicals having from 2 to 20 carbon atoms, said lubricant having a viscosity range of from 50 to 2,000 seconds Saybolt measured at 100 F.
  • a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow-relationship, a difiuoromonochloromethane refrigerant and alubricant soluble in said refrigerant comprising an organic acid ester of monopentaerythritol, and an organic acid selected from a group wherein the carboxyl group is attached to a radical taken from the group consisting of alkyl and aryl radicals having an average of from 6 to 10 carbon atoms, said lubricant having a viscosity range of from 50 to 2,000 seconds Saybolt measured at 4.
  • a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant fiow' ,relationship, a fluorochloro substituted aliphatic hydrogen refrigerant capable of being in the liquid and gaseous phases within the operating temperatures of said refrigeration apparatus, and a lubricant soluble in said refrigerant comprising an organic ester of pent-aerythri'tol which is a reaction product of monopentaerythritol and an organic acid selected from the group wherein the carboxyl group is attached to a radical taken from a group consisting of alkyl and aryl radicals having from about an average of 6 to 10 carbon atoms.
  • a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow relationship, a fluorochloro substituted aliphatic hydrogen refrigerant capable of being in the liquid and gaseous phases within the operating temperatures of said refrigeration apparatus, and a lubricant soluble in said refrigerant comprising an organic acid ester which is a reaction product of a pen-taerythritol selected from the group consisting of monopentaerythritol, dipentaerythritol and tripentaerythritol, and an organic acid selected from a group wherein the carboxyl group is attached to a radical taken from the group consisting of alkyl and aryl radicals having from 2 to 20 carbon atoms, said lubricant having a viscosity range of from to 2,000 seconds Saybolt measured at F.
  • a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow relationship, a fluorochloro substituted aliphatic hydrogen refrigerant capable of being in the liquid and gaseous phases within the operating temperatures of said refrigeration apparatus, and a lubricant soluble in said refrigerant comprising an organic acid ester which is a reaction product of monopentaerythritol and an organic acid selected from a group wherein the carboXyl group is attached to a radical taken from the group consisting of alkyl and aryl radicals having an average of from 6 to 10 carbon atoms, said lubricant having a viscosity range of from 50 to 2,000 seconds Saybolt measured at 100 F.

Description

Sept- 24, 1957 v. A. WlLLIAMlTlS 2,807,155
WORKING FLUIDS IN REFRIGERATION APPARATUS Filed Feb. 2, 1956 p 20- 53 'u 0 r; m w -20 t;
4o 0 PENT/IERYTHRICOL ESTER 0. 63 276,$05100F 80 I I' I I I0 20 30 40 .50 W7? CONCENTIZ/I T/ON, 0F LUBRICANT IN FREON 22 INVENTOR- VICTOR A. l/V/LLMM/ r15 ATTORNEY WORKING FLUIDS 1N REFRIGERATION APPARATUS 'Victor A. Williamitis, Dayton, Ohio, assignor to General Motors Corporation, Detroit, Mich., a corporation of Delaware Application February 2, 1956, Serial No. 563,038 6 Claims. (Cl. 62117.7)
' within the operating temperature range of the refrigeration apparatus and a wax-free lubricant which is completely soluble in the refrigerant and is highly thermally stable within the refrigeration apparatus in the range of the operating temperatures thereof. i
It is another object of this invention to provide a working fluid for a refrigeration apparatus which includes a lubricant comprising an organic acid ester of pentaerythritol and a refrigerant wherein the refrigerant is completely miscible with the ester and is capable of existing in liquid and gaseous phases within the operating temperature range of the refrigeration apparatus.
It is a further object of this invention to provide a working fluid for a refrigeration apparatus which includes a fluoro halo substituted aliphatic hydrocarbon refrigerant capable of being in liquid and gaseous phases within the operating temperature range of the refrigeration apparatus and a lubricant comprisingan organic acid ester of pentaerythritol.
It is yet another object of this invention to provide a refrigeration apparatus which includes a motor compressor, a condenser, an expansion device and evaporator in fluid flow relationship and a working fluid which includes a fluoro halo substituted aliphatichydrocarbon refrigerant and a lubricant comprising an organic acid ester of pentaerythritol.
Further objects and advantages of the present invention will be apparent from the following description, reference being had to the accompanying drawings wherein preferred embodiments of the present invention are clearly shown.
In the drawings:
Figure 1 is a diagrammatic representation of one type of refrigeration apparatus embodying this invention.
Figure 2 is a graph comparing Floc points or phase separation of various refrigeration lubricants and a'pentaerythritol ester at various concentrations in Freon 22.
A refrigeration apparatus embodying this invention is diagrammatically indicated in Figure l. Amotor. compressor unit 10 discharges compressed refrigerant, carrying some lubricant, through a pipe 12, to a condenser 14. The condensed refrigerant and lubricant then passes to an expansion device such as a capillary tube 16 and then to an evaporator 18. The vaporized mixture of refrigerant and lubricant flow through suction line 20 to the compressor 22 of the motor compressor .unit 10 wherein the vapor is compressed and discharged into dome 24 of the motor compressor unit. The compressed United States Patent O ice vapor is then discharged through pipe 12 for recirculation through the refrigeration apparatus. The compressor 22 is driven by an electric motor comprising a rotor 26 operatively connected to the compressor 22 by shaft 27 and a stator 28 secured to the containing 'member 30 of the motor compressor unit. The compressor 22 is preferably partially submerged in a body of lubricant 32 held in containing member 30 for lubricating the moving parts of the compressor. As above indicated, circulating refrigerant comes in direct contact with the lubricant in the motor compressor unit and carries small amounts of lubricant therewith throughout the refrigeration cycle. In operation, the temperature in the refrigeration apparatus may vary from about 100 F. at the end of the capillary tube or expansion device to about 400 F. at the compressor outlet.
Although the refrigeration apparatus described is of the high side type, i. e., the refrigerant enters containing member 30 directly at the compressor so that the fluid in dome 24 is under considerable pressure, it will be obvious that the present invention is also applicable to low side or other types of refrigeration apparatus.
The refrigerant used in the present invention preferably comprises a fluoro halo derivative of an aliphatic hydrocarbon of the character disclosed in the patent to Midgeley et al., -Re. 19,265, reissued August 7, 1934, as, for example, trichlorofluoromethane (Freon 11), dichlorodifluoromethane (Freon 12) and particularly difluoromonochloromethane (Freon 22).
The lubricant which is associated with the refrigerant throughout the refrigeration cycle has presented serious problems to satisfactory refrigeration operation in connection with certain otherwise useful refrigerants.
Among the requirements of a satisfactory refrigeration lubricant which may be mixed with a refrigerant to constitute a working fluid in a refrigeration apparatus of the type described, is that the lubricant be completely soluble in the particular refrigerant used throughout the range of operating temperatures, and that the lubricant be substantially free of wax, so as to prevent the precipitation of wax or. like substances with consequent blocking or restricting of the capillary tube and/or expansion valves at the low temperatures attained therein.
Various conventionally used mineral oils have been refined and dewaxed which have been eifective in minimizing Wax precipitation when used with certain refrigerants, such as Freon 12. However such oils are unsatisfactory to various degrees in this respect when used at very low temperatures with Freon 12 or with Freon 22 at any temperature in which such oils are only partially soluble. I
Other important requirements of a refrigerant lubricant are that the lubricant have high chemical and thermal stability in the presence of the refrigerant used, the metals, motor insulation winding and other materialswith which the lubricant comes into contact and is sealed.
It has been found that a combination of properties which to a high degree meet the requirements of a refrigeration system of the type described'exist in a class of compounds which may be broadly described as organic acid esters of pentaerythritol. More specifically the lubricant of the present invention may include esterified monomolecular pentaerythritol described by the following structural formula:
01120003 aoooiom-d-omdoo'n n'toojoa wherein the R represents a saturated aliphatic straight or--branched-hydrocarbon chain such as "alkyl radicals, and alkyl radicals having substituted aromatic radicals, aromatic groups such as aryl radicals and aryl radicals I v y having substituted aliphatic radicals, the R groups having carbon atoms in the range of about 2 to 20 and preferably an average of from 6 to 10. The term alkyl as hereinafter used includes both unsubstituted and aromatic radical substituted alkyl radicals and the trmaryl includes both unsubstituted and alkyl radical substituted aryl radicals.
The lubricant may also consist of or include the esterified polyethers diapentaerythritol and tripentaerythritol generally described by the following structural formulas:
| CHzOCOR CHZOCOR CHQOCOR wherein the R represents hydrocarbon groups as described above.
The pentaerythritol compounds may be produced by reacting acetaldehyde with formaldehyde in an alkaline medium under rigorously controlled conditions as is well described in chemical literature. The esters of the present invention may be formed by reacting the pentaerythritol compounds with organic acids having the desired hydrocarbon structures. Thus acids such as n-butyric, n-valeric and caprylic may be used to produce straight chained aliphatic R groups and acids such as isobutyric acid may be used to produce branched chain R groups. Similarly aromatic asids such as benzoic acid and paratoluic acid may be used to produce aryl R groups and acids such as phenylacetic acid may be used to produce aromatic radical substituted alkyl R groups. The acids used to produce the present esters are those having no reactive groups other than the carboxyl and preferably those having a single carboxyl group. The R groups mentioned in each molecule of the above-mentioned formulas may each be a different radical selected from the classes of radicals above described and are preferably varied. Further the lubricant preferably contains a mixture of different esters of the type described above selected so as to have a viscosity range from 50 to 2000 seconds Saybolt (SUS) measured as 100 F., the exact viscosity being dependent on the operating characteristics and the particular refrigerant of the refrigeration apparatus. Although it is not a strict requirement that all of the hydroxyl groups of the pentaerythritol compounds be esterified as shown in the above formulas, the compounds are preferably fully esterified.
The superiority of the present lubricant for refrigeration systems of the type described may be demonstrated by comparing the lubricant with conventionally used refrigeration mineral oil lubricants. The solubility of refrigeration lubricants is generally measured by mixing various percentages of the oil and a refrigerant in a glass pressure apparatus and externally cooling the same until phase separation or Floc point is noted. The graph of Figure 2 shows the temperature of the phase separation plotted against various concentrations of the oil and Freon 22 for lubricants of various viscosities. The refrigerant used in the comparison is Freon 22 since solution of the oil in this refrigerant is more diflicult than in other refrigerants.
The oil designated as A is a commercial refrigerant type naphthenic oil having the following specifications:
4 The oil designated as B is a commercial refrigerant type naphthenic oil having the following specifications:
Pour point, F., not above Color NPA, not darker than. 2.. Specific gravity at 00 F .9l2.0l9 Floc test (haze) F. l2+
10% oil by vol.) not above F.. 35
As shown in Figure 2 the Floc point of both oils A and B having a viscosity of 500 SUS at F. is at 84 F. at a concentration of 20% in Freon 22. The Floc point of oils A and B having a viscosity of SUS at 100 F. are at 46 F. and 34 F., respectively, at a concentration of 20% in Freon 22. In contrast the ;-Floc point of a mono pentaerythritol ester having a viscosity of 274 SUS at 100 F. and an average of about 7 aliphatic carbon atoms in the acid portion of the ester groups, is -63 F. at a concentration of 20% in Freon 22. I
The above described Floc tests are generally accepted as indicating low temperature performance of lubricants. Thus it is apparent that the use of the present pentaerythritol esters involve a substantial improvement in the opera tion of a refrigeration system at low temperatures, particularly with a refrigerant such as Freon 22.
The pentaerythritol esters of the present invention exhibit a high degree of thermal and chemical stability. The above A and B oils of comparable viscosity were compared by sealing the lubricant, Freon 22 and metal catalysts in pressurized glass tubes and exposing the combination to high temperatures the results of which are shown below..
Refrigerant decomposed Oil Thermal exposure in milligrams of released chlorine A 2weeks at 400 F 100 to 385 in various tests.
Pcntaerythritol ester d0 7.5.
In a similar test involving di 2, ethyl hexyl sebacate, a di ester, 520 milligrams of chlorine were measured in the thermal exposure of 1 week at 400 F. The pentaerythritol ester used in the above tests involves esters formed by reacting aliphatic organic acids having an average carbon chain of about 7.
Laboratory tests also indicate that the ASTM viscosity index of the above pentaerythritol esters is 119.5 as compared to viscosity indexes of under 20 for the above A and B oils indicating that the subject lubricant Varies considerably less with temperatures than conventionally used lubricants with obvious advantage.
While the embodiments of the present invention as herein disclosed constitute preferred forms, it is to be understood that other forms might be adopted.
What is claimed is as follows:
1. In combination, a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow relationship, a difluoromonochloromethane refrigerant and a lubricant soluble in said refrigerant comprising an organic ester of pentaerythritol which is a reaction product of monopentaerythritol and an organic acid selected from the group wherein the carboxyl group is attached to a radical taken from a group consisting of alkyl and aryl radicals having an average of from 6 to 10 carbon atoms.
2. In combination, a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow relationship, a difluoromonochloromethane refrigerant and a lubricant soluble in said refrigerant comprising an organic acid ester which is a reaction product of a pentaerythritol selected from the group consisting of monopentaerythritol, dipentaerythritol and tripentaerythritol, and an organic acid selected from a group wherein the carboXyl group is attached to a radical taken from the group consisting of alkyl and aryl radicals having from 2 to 20 carbon atoms, said lubricant having a viscosity range of from 50 to 2,000 seconds Saybolt measured at 100 F.
3. In combination, a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow-relationship, a difiuoromonochloromethane refrigerant and alubricant soluble in said refrigerant comprising an organic acid ester of monopentaerythritol, and an organic acid selected from a group wherein the carboxyl group is attached to a radical taken from the group consisting of alkyl and aryl radicals having an average of from 6 to 10 carbon atoms, said lubricant having a viscosity range of from 50 to 2,000 seconds Saybolt measured at 4. In '-cornbination, a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant fiow' ,relationship, a fluorochloro substituted aliphatic hydrogen refrigerant capable of being in the liquid and gaseous phases within the operating temperatures of said refrigeration apparatus, and a lubricant soluble in said refrigerant comprising an organic ester of pent-aerythri'tol which is a reaction product of monopentaerythritol and an organic acid selected from the group wherein the carboxyl group is attached to a radical taken from a group consisting of alkyl and aryl radicals having from about an average of 6 to 10 carbon atoms.
5. In combination, a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow relationship, a fluorochloro substituted aliphatic hydrogen refrigerant capable of being in the liquid and gaseous phases within the operating temperatures of said refrigeration apparatus, and a lubricant soluble in said refrigerant comprising an organic acid ester which is a reaction product of a pen-taerythritol selected from the group consisting of monopentaerythritol, dipentaerythritol and tripentaerythritol, and an organic acid selected from a group wherein the carboxyl group is attached to a radical taken from the group consisting of alkyl and aryl radicals having from 2 to 20 carbon atoms, said lubricant having a viscosity range of from to 2,000 seconds Saybolt measured at F.
6. In combination, a refrigeration apparatus including a compressor, condenser, and evaporator in refrigerant flow relationship, a fluorochloro substituted aliphatic hydrogen refrigerant capable of being in the liquid and gaseous phases within the operating temperatures of said refrigeration apparatus, and a lubricant soluble in said refrigerant comprising an organic acid ester which is a reaction product of monopentaerythritol and an organic acid selected from a group wherein the carboXyl group is attached to a radical taken from the group consisting of alkyl and aryl radicals having an average of from 6 to 10 carbon atoms, said lubricant having a viscosity range of from 50 to 2,000 seconds Saybolt measured at 100 F.
References Cited in the file of this patent UNITED STATES PATENTS 2,524,590 Boe Oct. 3, 1950 2,564,423 Barnum Aug. 14, 1951 2,580,654 Browning Jan. 1, 1952 2,652,361 Woods et a1 Sept. 15, 1953 2,663,999 Alsing Dec. 29, 1953 OTHER REFERENCES Kinetic Chemicals, Technical Bulletin B-2 on Freon Compounds (1950), pages 6 and 8.

Claims (1)

1. IN COMBINATION, A REFRIGERATION APPARATUS INCLUDING A COMPRESSOR, CONDENSER, AND EVAPORATOR IN REFRIGERANT FLOW RELATIONSHIP, A DIFLUOROMONOCHLOROMETHANE REFRIGERANT AND A LUBRICANT SOLUBLE IN SAID REFRIGERANT COMPRISING AN ORGANIC ESTER OF PENTAERYTHRITOL WHICH IS A REACTION PRODUCT OF MONOPENTAERYTHRITOL AND AN ORGANIC ACID SELECTED FROM THE GROUP WHEREIN THE CARBOXYL GROUP IS ATTACHED TO A RADICAL TAKEN FROM A GROUP CONSISTING ALKYL AND ARYL RADICALS HAVING AN AVERAGE OF FROM 6 TO 10 CARBON ATOMS.
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Cited By (30)

* Cited by examiner, † Cited by third party
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US3496992A (en) * 1961-05-25 1970-02-24 Carrier Corp Method and apparatus for heating and cooling
JPS49109771A (en) * 1973-01-22 1974-10-18
FR2388227A1 (en) * 1977-04-22 1978-11-17 Westinghouse Electric Corp CENTRIFUGAL REFRIGERATING COMPRESSOR SYSTEMS
US4172178A (en) * 1978-05-05 1979-10-23 Westinghouse Electric Corp. Impregnated castings chemically resistant to contact with halocarbon refrigerant
EP0435253A1 (en) * 1989-12-28 1991-07-03 Nippon Oil Company, Limited Refrigerator oils for use with hydrogen-containing halogenocarbon refrigerants
EP0445611A1 (en) * 1990-03-05 1991-09-11 Hoechst Aktiengesellschaft Use of ester oils as lubricant for refrigerant compressor
EP0448402A2 (en) * 1990-03-23 1991-09-25 Asahi Denka Kogyo Kabushiki Kaisha Refrigerator oil composition
EP0458584A1 (en) * 1990-05-22 1991-11-27 Unichema Chemie B.V. Lubricants
JPH03505602A (en) * 1989-04-25 1991-12-05 ザ ルブリゾル コーポレイション Liquid composition containing carboxylic acid ester
WO1992001030A1 (en) * 1990-07-12 1992-01-23 Henkel Corporation Lubricant for refrigerant heat transfer fluids
EP0468729A1 (en) * 1990-07-23 1992-01-29 Castrol Limited Lubrication of vapour compression heat transfer systems
EP0470788A1 (en) * 1990-08-07 1992-02-12 Nippon Oil Co., Ltd. Synthetic lubricating oil
EP0475751A1 (en) * 1990-09-12 1992-03-18 Kao Corporation Working fluid composition for refrigerating machine
EP0499994A1 (en) * 1991-02-19 1992-08-26 DEA Mineraloel Aktiengesellschaft Lubricant for refrigerators
JPH0617073A (en) * 1992-07-04 1994-01-25 Kao Corp Working fluid composition for refrigerator
EP0645443A2 (en) * 1991-01-30 1995-03-29 Hitachi, Ltd. Refrigeration compressor and its operating
EP0688854A1 (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
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US5820777A (en) * 1993-03-10 1998-10-13 Henkel Corporation Blended polyol ester lubricants for refrigerant heat transfer fluids
US5830833A (en) * 1992-08-18 1998-11-03 Rwe-Dea Aktiengesellschaft Fur Mineraloel Und Chemie And Texaco Deutschland Gmbh Synthetic ester lubricants for refrigerator systems
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
US20030199401A1 (en) * 1999-07-06 2003-10-23 Idemitsu Kosan Co., Ltd. Refrigerating machine oil composition for carbon dioxide refrigerant
US6998065B1 (en) * 1989-12-28 2006-02-14 Nippon Mitsubishi Oil Corporation Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants
US7018558B2 (en) 1999-06-09 2006-03-28 Cognis Corporation Method of improving performance of refrigerant systems
US7052626B1 (en) * 1989-12-28 2006-05-30 Nippon Mitsubishi Oil Corporation Fluid compositions containing refrigeration oils and chlorine-free fluorocarbon refrigerants

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2524590A (en) * 1946-04-22 1950-10-03 Carsten F Boe Emulsion containing a liquefied propellant gas under pressure and method of spraying same
US2564423A (en) * 1948-05-29 1951-08-14 Shell Dev Corrosion preventive composition
US2580654A (en) * 1949-10-26 1952-01-01 Standard Oil Co Grease dispersion
US2652361A (en) * 1951-12-29 1953-09-15 Shell Dev Grease compositions
US2663999A (en) * 1952-02-18 1953-12-29 Seeger Refrigerator Co Household refrigerator

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2524590A (en) * 1946-04-22 1950-10-03 Carsten F Boe Emulsion containing a liquefied propellant gas under pressure and method of spraying same
US2564423A (en) * 1948-05-29 1951-08-14 Shell Dev Corrosion preventive composition
US2580654A (en) * 1949-10-26 1952-01-01 Standard Oil Co Grease dispersion
US2652361A (en) * 1951-12-29 1953-09-15 Shell Dev Grease compositions
US2663999A (en) * 1952-02-18 1953-12-29 Seeger Refrigerator Co Household refrigerator

Cited By (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3496992A (en) * 1961-05-25 1970-02-24 Carrier Corp Method and apparatus for heating and cooling
JPS49109771A (en) * 1973-01-22 1974-10-18
JPS5928239B2 (en) * 1973-01-22 1984-07-11 ヘンケル・コマンデイトゲゼルシヤフト・アウフ・アクテイーン Lubricants and hydraulic fluids using new ester oils
FR2388227A1 (en) * 1977-04-22 1978-11-17 Westinghouse Electric Corp CENTRIFUGAL REFRIGERATING COMPRESSOR SYSTEMS
JPS53143609A (en) * 1977-04-22 1978-12-14 Westinghouse Electric Corp Centrifugal compressor apparatus for refrigeration
US4159255A (en) * 1977-04-22 1979-06-26 Westinghouse Electric Corp. Modified castor oil lubricant for refrigerator systems employing halocarbon refrigerants
JPS5835557B2 (en) * 1977-04-22 1983-08-03 マツクエイ−パ−フエツクス インコ−ポレイテツド Lubricant composition for centrifugal refrigeration compressor equipment
US4172178A (en) * 1978-05-05 1979-10-23 Westinghouse Electric Corp. Impregnated castings chemically resistant to contact with halocarbon refrigerant
JPH03505602A (en) * 1989-04-25 1991-12-05 ザ ルブリゾル コーポレイション Liquid composition containing carboxylic acid ester
JPH09111229A (en) * 1989-04-25 1997-04-28 Lubrizol Corp:The Liquid composition containing carboxylic ester
JP2624893B2 (en) 1989-04-25 1997-06-25 ザ ルブリゾル コーポレイション Liquid composition containing carboxylic acid ester
US7052626B1 (en) * 1989-12-28 2006-05-30 Nippon Mitsubishi Oil Corporation Fluid compositions containing refrigeration oils and chlorine-free fluorocarbon refrigerants
EP0435253A1 (en) * 1989-12-28 1991-07-03 Nippon Oil Company, Limited Refrigerator oils for use with hydrogen-containing halogenocarbon refrigerants
US6998065B1 (en) * 1989-12-28 2006-02-14 Nippon Mitsubishi Oil Corporation Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants
EP0445611A1 (en) * 1990-03-05 1991-09-11 Hoechst Aktiengesellschaft Use of ester oils as lubricant for refrigerant compressor
EP0448402A2 (en) * 1990-03-23 1991-09-25 Asahi Denka Kogyo Kabushiki Kaisha Refrigerator oil composition
EP0448402A3 (en) * 1990-03-23 1991-10-23 Asahi Denka Kogyo Kabushiki Kaisha Refrigerator oil composition
US5211884A (en) * 1990-05-22 1993-05-18 Unilever Patent Holdings Bv Lubricants
EP0458584A1 (en) * 1990-05-22 1991-11-27 Unichema Chemie B.V. Lubricants
WO1992001030A1 (en) * 1990-07-12 1992-01-23 Henkel Corporation Lubricant for refrigerant heat transfer fluids
JPH04248099A (en) * 1990-07-23 1992-09-03 Castrol Ltd Lubricating method
US5229025A (en) * 1990-07-23 1993-07-20 Castrol Limited Lubrication and a method of retrofilling a working fluid/lubricant composition
EP0468729A1 (en) * 1990-07-23 1992-01-29 Castrol Limited Lubrication of vapour compression heat transfer systems
EP0470788A1 (en) * 1990-08-07 1992-02-12 Nippon Oil Co., Ltd. Synthetic lubricating oil
EP0475751A1 (en) * 1990-09-12 1992-03-18 Kao Corporation Working fluid composition for refrigerating machine
US5202044A (en) * 1990-09-12 1993-04-13 Kao Corporation Working fluid composition for refrigerating machine
EP0688855A1 (en) * 1990-11-16 1995-12-27 Hitachi, Ltd. Refrigerating apparatus and refrigerant compressor
US5711165A (en) * 1990-11-16 1998-01-27 Hitachi, Ltd. Refrigerating apparatus and refrigerant compressor
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US5964581A (en) * 1990-11-16 1999-10-12 Hitachi, Ltd. Refrigerant compressor
US6029459A (en) * 1990-11-16 2000-02-29 Hitachi, Ltd. Refrigeration cycle
US6258293B1 (en) 1990-11-16 2001-07-10 Hitachi, Ltd. Refrigeration cycle
EP0779354A1 (en) * 1990-12-27 1997-06-18 Matsushita Refrigeration Company Refrigerating system for refrigerator
US5486302A (en) * 1991-01-17 1996-01-23 Cpi Engineering Services, Inc. Lubricant composition for fluorinated refrigerants used in compression refrigeration systems
US5612299A (en) * 1991-01-17 1997-03-18 Cpi Engineering Services, Inc. Lubricant composition for fluorinated refrigerants used in compression refrigeration systems
US5553465A (en) * 1991-01-30 1996-09-10 Hitachi, Ltd. Refrigeration apparatus containing lubricant composition
EP0645443A2 (en) * 1991-01-30 1995-03-29 Hitachi, Ltd. Refrigeration compressor and its operating
EP0645443A3 (en) * 1991-01-30 1995-04-19 Hitachi Ltd
US5445753A (en) * 1991-01-30 1995-08-29 Hitachi, Ltd. Lubricant for refrigeration compressors
EP0499994A1 (en) * 1991-02-19 1992-08-26 DEA Mineraloel Aktiengesellschaft Lubricant for refrigerators
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
US6296782B1 (en) 1992-06-03 2001-10-02 Henkel Corporation Polyol ester lubricants for refrigerator compressors operating at high temperatures
US6551524B2 (en) 1992-06-03 2003-04-22 Cognis Corporation Polyol ester lubricants, especially those compatible with mineral oils, for refrigerating compressors operating at high temperatures
US5906769A (en) * 1992-06-03 1999-05-25 Henkel Corporation Polyol ester lubricants for refrigerating compressors operating at high temperatures
US6666985B2 (en) 1992-06-03 2003-12-23 Cognis Corporation Polyol ester lubricants for hermetically sealed refrigerating compressors
JPH0617073A (en) * 1992-07-04 1994-01-25 Kao Corp Working fluid composition for refrigerator
US5830833A (en) * 1992-08-18 1998-11-03 Rwe-Dea Aktiengesellschaft Fur Mineraloel Und Chemie And Texaco Deutschland Gmbh Synthetic ester lubricants for refrigerator 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
US6551523B1 (en) 1995-06-07 2003-04-22 Cognis Corporation Blended polyol ester lubricants for refrigerant heat transfer fluids
US7018558B2 (en) 1999-06-09 2006-03-28 Cognis Corporation Method of improving performance of refrigerant systems
US20030199401A1 (en) * 1999-07-06 2003-10-23 Idemitsu Kosan Co., Ltd. Refrigerating machine oil composition for carbon dioxide refrigerant
US7018961B2 (en) * 1999-07-06 2006-03-28 Idemitsu Kosan Co., Ltd. Refrigerating machine oil composition for carbon dioxide refrigerant
US20060128576A1 (en) * 1999-07-06 2006-06-15 Idemitsu Kosan Co., Ltd. Refrigerating machine oil composition for carbon dioxide refrigerant
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