US2807155A - Working fluids in refrigeration apparatus - Google Patents
Working fluids in refrigeration apparatus Download PDFInfo
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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
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- compressor
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- 238000005057 refrigeration Methods 0.000 title claims description 38
- 239000012530 fluid Substances 0.000 title description 9
- 239000003507 refrigerant Substances 0.000 claims description 48
- 239000000314 lubricant Substances 0.000 claims description 41
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 22
- -1 CARBOXYL GROUP Chemical group 0.000 claims description 21
- 229940059574 pentaerithrityl Drugs 0.000 claims description 19
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims description 15
- 150000005840 aryl radicals Chemical class 0.000 claims description 9
- 150000003254 radicals Chemical class 0.000 claims description 9
- 150000007524 organic acids Chemical class 0.000 claims description 8
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- 150000002895 organic esters Chemical class 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 239000003921 oil Substances 0.000 description 15
- 125000000217 alkyl group Chemical group 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 239000007792 gaseous phase Substances 0.000 description 5
- 239000007791 liquid phase Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 4
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 4
- PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000005191 phase separation Methods 0.000 description 3
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- LPNBBFKOUUSUDB-UHFFFAOYSA-N p-toluic acid Chemical compound CC1=CC=C(C(O)=O)C=C1 LPNBBFKOUUSUDB-UHFFFAOYSA-N 0.000 description 2
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 2
- PIMNDJYXVOQVSP-UHFFFAOYSA-N 1-o-ethyl 10-o-hexyl decanedioate Chemical compound CCCCCCOC(=O)CCCCCCCCC(=O)OCC PIMNDJYXVOQVSP-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- 239000000026 Pentaerythritol tetranitrate Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 229960003424 phenylacetic acid Drugs 0.000 description 1
- 239000003279 phenylacetic acid Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Images
Classifications
-
- 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
-
- 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
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/38—Esters 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;
' 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.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US563038A US2807155A (en) | 1956-02-02 | 1956-02-02 | Working fluids in refrigeration apparatus |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US563038A US2807155A (en) | 1956-02-02 | 1956-02-02 | Working fluids in refrigeration apparatus |
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US2807155A true US2807155A (en) | 1957-09-24 |
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US563038A Expired - Lifetime US2807155A (en) | 1956-02-02 | 1956-02-02 | Working fluids in refrigeration apparatus |
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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 |
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JPS49109771A (en) * | 1973-01-22 | 1974-10-18 | ||
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US4172178A (en) * | 1978-05-05 | 1979-10-23 | Westinghouse Electric Corp. | Impregnated castings chemically resistant to contact with halocarbon refrigerant |
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US6998065B1 (en) * | 1989-12-28 | 2006-02-14 | Nippon Mitsubishi Oil Corporation | Fluid compositions containing refrigerator oils and chlorine-free fluorocarbon refrigerants |
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US5229025A (en) * | 1990-07-23 | 1993-07-20 | Castrol Limited | Lubrication and a method of retrofilling a working fluid/lubricant composition |
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