Process for refrigeration using 1,1,1,2-tetrafluoro-2-(difluoromethoxy) ethane or 1,1,2,2-tetrafluoro-2-(difluoromethoxy)ethane

Information

  • Patent Grant
  • 5474696
  • Patent Number
    5,474,696
  • Date Filed
    Thursday, November 10, 1994
    29 years ago
  • Date Issued
    Tuesday, December 12, 1995
    28 years ago
Abstract
Producing refrigeration by evaporating the fluorocarbon refrigerants 1,1,1,2- and 1,1,2,2-tetrafluoro-2-(difluoromethoxy)ethane in the vicinity of a body to be cooled.
Description

BACKGROUND OF THE INVENTION
The present invention relates to a process for refrigeration using a chlorine-free fluorocarbon refrigerant.
A refrigeration system is designed to produce a cooling effect and is used for air conditioning buildings and in the treatment transportation and preservation of foods. During a refrigeration cycle the refrigerant undergoes a physical change resulting in a cooling effect, for example, a change from the liquid state to the vapor state. A simple refrigeration system is generally closed and consists of four major components, namely an evaporator, a compressor, a condenser and an expansion device. During the refrigeration cycle the refrigerant in liquid form leaves the condenser and passes through the expansion device where the pressure is lowered. The refrigerant passes into the evaporator where heat is absorbed and the refrigerant evaporates. The refrigerant leaves the evaporator as vapor and enters the compressor where it is compressed to a superheated vapor before passing into the condenser to complete the cycle, which is repeated continuously.
The most widely used refrigerants are known as chlorofluorocarbons (CFCs). These compounds are fully halogenated, very stable, have low toxicity and excellent thermodynamic performance in use. Unfortunately, CFCs, because of their stability, have long atmospheric lifetimes. It has been postulated that when these materials decompose in the stratosphere, under the influence of ultraviolet radiation, they release chlorine atoms which, it is theorized, react with the ozone thus depleting this protective layer which shields the earth from harmful ultraviolet radiation.
There is a need for fluorocarbon refrigerants that are substantially chlorine-free and environmentally safe, non-flammable, have low toxicity and excellent thermodynamic properties, especially its refrigeration capacity at a given evaporator temperature, and a high coefficient of performance.
SUMMARY OF THE INVENTION
The present invention is directed to a process for producing refrigeration which comprises condensing a chlorine-free fluorocarbon refrigerant selected from the group consisting of 1,1,1,2-tetrafluoro-2-(difluoromethoxy)ethane (CHF.sub.2 OCHFCF.sub.3), and 1,1,2,2-tetrafluoro-2-(difluoromethoxy)ethane (CHF.sub.2 OCF.sub.2 CHF.sub.2), and thereafter evaporating the fluorocarbon refrigerant in the vicinity of a body to be cooled. The chlorine-free fluorocarbons are environmentally safe while, at the same time, they show excellent thermodynamic properties when measured against commercially successful refrigerants.





DESCRIPTION OF PREFERRED EMBODIMENTS
The chlorine-free fluorocarbon refrigerants used in the process of the invention are 1,1,1,2-tetrafluoro-2-(difluoromethoxy)ethane and 1,1,2,2-tetrafluoro-2-(difluoromethoxy)ethane. The procedure for preparing the fluorocarbon refrigerants of the present invention are known in the art. 1,1,1,2-Tetrafluoro-2-(difluoromethoxy)ethane can be prepared by reacting isoflurane (CHF.sub.2 OCHClF.sub.3) with hydrogen fluoride in the presence of an antimony pentachloride catalyst wherein the molar ratio of isoflurane to hydrogen fluoride is about 1:2, as disclosed in European Patent Application 388,114. 1,1,2,2-Tetrafluoro-2-(difluoromethoxy)ethane can be prepared by chlorinating CH.sub.3 OCF.sub.2 CHF.sub.2 to CHCl.sub.2 OCF.sub.2 CHF.sub.2 followed by the exchange of chlorine for fluorine, as described in Terrell et al., J. Med. Chem., Vol. 15, pp. 604-606 (1972). 1,1,2,2-Tetrafluoro-2-(difluoromethoxy)ethane can also be prepared by electrochemical fluorination of CHCl.sub.2 OCF.sub.2 CHClF as described by Okazaki et al., J. Fluorine Chem. Vol. 4, pp. 387-397 (1974).
The process of the present invention involves transferring heat in a refrigeration cycle by repeatedly evaporating, compressing and condensing in a closed system the chlorine-free fluorocarbons 1,1,1,2- and 1,1,2,2-tetrafluoro-2-(difluoromethoxy)ethane.
The fluorocarbon refrigerant 1,1,1,2-tetrafluoro-2-(difluoromethoxy)ethane is reported to have a boiling point at 23.5.degree. C. The fluorocarbon refrigerant 1,1,2,2-tetrafluoro-2-(difluoromethoxy)ethane has a boiling point at atmospheric pressure of 28.5.degree. C.
Additional chlorine-free fluorocarbon refrigerants can be added to the fluorocarbon refrigerants in varying amounts, for example, to improve thermodynamic properties of the mixture or to incorporate the fluorocarbons composition of the present invention with flammable mixtures to lower their flammability. Such refrigerants include hydrofluoroalkanes, hydrofluoroethers, cyclic hydrofluoroalkanes, cyclic hydrofluoroethers. The addition of such other ingredients does not detract from the benefits of the chlorine-free fluorocarbons used in the present invention.
The advantages of the invention can be seen when 1,1,1,2-tetrafluoro-2-(difluoromethoxy)ethane (CHF.sub.2 OCHFCF.sub.3) and 1,1,2,2-tetrafluoro-2-(difluoromethoxy)ethane (CHF.sub.2 OCF.sub.2 CHF.sub.2) are compared with the performance of the commercially successful refrigerant trichlorofluoromethane (CFC-11) in regard to coefficient of performance and capacity as illustrated in Table I below.
TABLE I______________________________________CFC-11 (CHF.sub.2 OCHFCF.sub.3) (CHF.sub.2 OCF.sub.2 CHF.sub.2)______________________________________Evaporator 40 40 40Temp., .degree.F.Evaporator 7.11 6.79 5.44Pressure,psiaCondenser 100 100 100Temp., .degree.F.Condenser 23.53 24.85 20.54Pressure,psiaReturn Gas 60 60 60Temp., .degree.F.Compres- 131.2 105.2 109.6sorDischargeTemp., .degree.F.Coefficient 7.27 6.79 6.93ofPerform-anceCapacity - 42.37 39.7 33.5BTU/min.Vapor 15.4 15.7 12.9Pressureat 25.degree. C.,psiaImpeller 132.8 151.0 151.8TipSpeed, m/s______________________________________
The coefficient of performance is the ratio of the capacity to the compressor work. It measures refrigerant energy efficiency.
Capacity means the change in enthalpy of the refrigerant in the evaporator per pound of refrigerant circulated, i.e., the heat removed by the refrigerant in the evaporator per time.
Impeller tip speed means the speed needed to compress a refrigerant from saturated vapor at 40.degree. F. to a pressure corresponding to a condensing temperature of 100.degree. F.
The coefficient of performance and capacity for the chlorine-free fluorocarbons of this invention are compared to CFC-11 in Table I above. It can be seen that the capacity and coefficient of performance values for the environmentally safe chlorine-free fluorocarbon refrigerants are comparable to those for the commercially successful refrigerant CFC-11.
Claims
  • 1. A process for producing refrigeration which comprises condensing a chlorine-free fluorocarbon refrigerant selected from the group consisting of 1,1,1,2-tetrafluoro-2-(difluoromethoxy)ethane and 1,1,2,2-tetrafluoro-2-(difluoromethoxy)ethane, and thereafter evaporating the fluorocarbon refrigerant in the vicinity of a body to be cooled.
  • 2. A process of claim 1 wherein the fluorocarbon refrigerant is 1,1,1,2-tetrafluoro-2-(difluoromethoxy)ethane.
  • 3. A process of claim 1 wherein the fluorocarbon refrigerant is 1,1,2,2-tetrafluoro-2-(difluoromethoxy)ethane.
Parent Case Info

This is a continuation of application Ser. No. 08/008,263 filed on Jan. 25, 1993, now abandoned, which is a continuation of patent application Ser. No. 07/758,269 on Aug. 27, 1991, abandoned.

US Referenced Citations (9)
Number Name Date Kind
3362180 Eiseman, Jr. Jan 1968
3394878 Eiseman Jul 1968
3409555 Eiseman Nov 1968
4541943 Powell Sep 1985
4559154 Powell Dec 1985
4762856 Terrell Aug 1988
4961321 O'Neill et al. Oct 1990
4985169 Rolland et al. Jan 1991
5023009 Merchant Jun 1991
Foreign Referenced Citations (2)
Number Date Country
0127365 Dec 1984 EPX
0388114 Sep 1990 EPX
Non-Patent Literature Citations (3)
Entry
McLinden et al, "Quest for Alternatives", ASHRAE Journal, Dec. 1987.
Journal of Medicinal Chemistry, 1972, vol. 15, No. 6, by Terrell et al., pp. 604-606, "General Anesthetics. 3. Fluorinated Methyl Ethyl Ethers as Anesthetic Agents".
International Search Report regarding international application No. PCT/US92/06973 with an international filing date of Aug. 25, 1992.
Continuations (2)
Number Date Country
Parent 8263 Jan 1993
Parent 758269 Aug 1991