US20170233624A1 - Fluorinated alkene refrigerant compositions - Google Patents

Fluorinated alkene refrigerant compositions Download PDF

Info

Publication number
US20170233624A1
US20170233624A1 US15/389,697 US201615389697A US2017233624A1 US 20170233624 A1 US20170233624 A1 US 20170233624A1 US 201615389697 A US201615389697 A US 201615389697A US 2017233624 A1 US2017233624 A1 US 2017233624A1
Authority
US
United States
Prior art keywords
fluoroalkene
composition
lubricant
refrigerant
polyalkylene glycol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US15/389,697
Inventor
Raymond H. Thomas
Rajiv R. Singh
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Honeywell International Inc
Original Assignee
Honeywell International Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34549972&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US20170233624(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Honeywell International Inc filed Critical Honeywell International Inc
Priority to US15/389,697 priority Critical patent/US20170233624A1/en
Assigned to HONEYWELL INTERNATIONAL INC. reassignment HONEYWELL INTERNATIONAL INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SINGH, RAJIV R., THOMAS, RAYMOND H.
Publication of US20170233624A1 publication Critical patent/US20170233624A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • 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
    • C09K5/045Materials 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 containing only fluorine as halogen
    • 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
    • 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
    • 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
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/20Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
    • C10M107/30Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M107/32Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
    • C10M107/34Polyoxyalkylenes
    • 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
    • C10M111/00Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
    • C10M111/02Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a non-macromolecular organic compound
    • 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
    • C10M111/00Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
    • C10M111/04Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
    • 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
    • C09K2205/00Aspects relating to compounds used in compression type refrigeration systems
    • C09K2205/10Components
    • C09K2205/12Hydrocarbons
    • C09K2205/126Unsaturated fluorinated hydrocarbons
    • 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
    • C09K2205/00Aspects relating to compounds used in compression type refrigeration systems
    • C09K2205/24Only one single fluoro component present
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • C10M2207/2835Esters of polyhydroxy compounds used as base material
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/287Partial esters
    • C10M2207/289Partial esters containing free hydroxy groups
    • C10M2207/2895Partial esters containing free hydroxy groups used as base material
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/1033Polyethers, i.e. containing di- or higher polyoxyalkylene groups used as base material
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/109Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
    • C10M2209/1095Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified used as base material
    • 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
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/02Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
    • C10M2211/022Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
    • C10M2211/0225Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic used as base material
    • 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
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated compounds
    • C10M2211/063Perfluorinated compounds used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/09Characteristics associated with water
    • C10N2020/097Refrigerants
    • C10N2020/101Containing Hydrofluorocarbons
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/30Refrigerators lubricants or compressors lubricants
    • C10N2220/302
    • C10N2240/30

Abstract

Liquid compositions for use in compression refrigeration, air-conditioning and heat pump systems in which a fluoroalkene containing from 3 to 4 carbon atoms and at least 1 but no more than 2 double bonds is combined with an effective amount to provide lubrication of an essentially miscible organic lubricant comprised of carbon, hydrogen and oxygen and having a ratio of oxygen to carbon effective to provide a degree of miscibility with said fluoroalkene so that when up to five weight percent of lubricant is added to said fluoroalkene the refrigerant has one liquid phase at least one temperature between −40 and +70° C. Methods for producing refrigeration and heating with the fluoroalkenes, alone or in combination with the disclosed lubricants, are also disclosed.

Description

    RELATED APPLICATIONS
  • The present application is a division of U.S. application Ser. No. 11/385,259, filed Mar. 20, 2006 which application is a continuation of U.S. application Ser. No. 10/695,212, filed Oct. 27, 2003, (abandoned) which is incorporated herein by reference.
  • The present application is also related to and claims the priority benefit of U.S. Provisional Application Nos. 60/421,263, and 60/421,435, each of which was filed on Oct. 25, 2002 and each of which is incorporated herein by reference. The present application is also related to and incorporates by reference each of the following filed U.S. patent applications: application Ser. No. 10/694,273 entitled “COMPOSITIONS CONTAINING FLUORINE SUBSTITUTED OLEFINS,” by Singh et al., (now U.S. Pat. No. 7,534,355, issued May 19, 2009), and application Ser. No. 10/694,272 entitled “PROCESS FOR PRODUCING FLUOROPROPENES,” by Tung et al., (now U.S. Pat. No. 7,230,146, issued Jun. 12, 2007).
  • FIELD OF THE INVENTION
  • The present invention relates to compositions used as refrigeration fluids in compression refrigeration, air-conditioning and heat pump systems.
  • BACKGROUND OF THE INVENTION
  • The use of chlorine-containing refrigerants, such as chlorofluorocarbons (CFC's), hydrochlorofluorocarbons (HCF's) and the like, as refrigerants in air-conditioning and refrigeration systems has become disfavored because of the ozone-depleting properties associated with such compounds. As a result, it has become desirable to retrofit chlorine-containing refrigeration systems by replacing chlorine-containing refrigerants with non-chlorine-containing refrigerant compounds that will not deplete the ozone layer, such as hydrofluorocarbons (HFC's).
  • In order for any of the replacement materials to be useful in connection with refrigeration compositions, the materials must be compatible with the lubricant utilized in the compressor. Unfortunately, many non-chlorine-containing refrigeration fluids, including HFC's, are relatively insoluble and/or immiscible in the types of lubricants used traditionally with CFC's and HFC's, including, for example, mineral oils, alkylbenzenes or poly(alpha-olefins). In order for a refrigeration fluid-lubricant combination to work efficiently within a compression refrigeration, air-conditioning or heat pump system, the lubricant must be sufficiently soluble in the refrigeration liquid over a wide range of operating temperatures. Such solubility lowers the viscosity of the lubricant and allows it to flow more easily throughout the system. In the absence of such solubility, lubricants tend to become lodged in the coils of the compression refrigeration, air-conditioning or heat pump system evaporator, as well as other parts of the system, and thus reduce the system efficiency.
  • Polyalkylene glycol, esterified polyalkylene glycol, and polyol ester lubricating oils have been developed as misicible lubricants for HFC refrigeration liquids. Polyalkylene glycol refrigeration lubricants are disclosed by U.S. Pat. Nos. 4,755,316; 4,971,712, and 4, 975, 212. Polyalkylene glycol esters are disclosed by U.S. Pat. No. 5,008,028. The polyalkylene glycol and polyalkylene glycol ester lubricating oils are disclosed as being misicible in fluoroalkanes containing one or two carbon atoms and no double bonds.
  • Consequently fluorocarbon-based fluids have found widespread use in industry for refrigeration system applications, including air-conditioning systems and heat pump applications as well, all of which involve compression refrigeration. Compression refrigeration generally involves changing the refrigerant from the liquid to the vapor phase through heat adsorption at a lower pressure and then from the vapor to the liquid phase through heat removal at an elevated pressure.
  • While the primary purpose of refrigeration is to remove energy at low temperature, the primary purpose of a heat pump is to add energy at higher temperature. Heat pumps are considered reverse cycle systems because for heating, the operation of the condenser is interchanged with that of the refrigeration evaporator.
  • The art is continually seeking new fluorocarbon and hydrofluorocarbon-based pure fluids that offer alternatives for refrigeration and heat pump applications. Applicants have come to appreciate that fluoro-olefin-based materials (fluoroalkenes) are of particular interest because they have characteristics that make them environmentally safer substitutes for the presently used fluoroalkanes (HFC's), that despite being safe for the ozone layer are suspected of causing global warming.
  • Applicant has also come to recognize that refrigeration composition substitutes for HFC's in many cases preferably possess certain performance properties to be considered acceptable substitutes, including acceptable refrigeration characteristics, chemical stability, low toxicity, non-flammability, lubricant compatibility and efficiency in use. The latter characteristic is important in many refrigeration systems, air-conditioning systems and heat pump applications, especially when a loss in refrigeration thermodynamic performance or energy efficiency may have secondary environmental impacts through increased fossil fuel usage arising from an increased demand for electrical energy. Furthermore, it would be advantageous for HFC refrigeration composition substitutes to not require major engineering changes to conventional vapor compression technology and lubricant systems currently used with HFC refrigeration liquids.
  • Flammability is another important property for many applications. That is, it is considered either important or essential in many applications, including particularly in heat transfer applications, to use compositions which are non-flammable. Thus, it is frequently beneficial to use in such compositions compounds which are nonflammable. As used herein, the term “nonflammable” refers to compounds or compositions which are determined to be nonflammable in accordance with ASTM standard E-681, dated 2002, which is incorporated herein by reference. Unfortunately, many HFC's which might otherwise be desirable for used in refrigerant compositions are not nonflammable. For example, the fluoroalkane difluoroethane (HFC-152a) and the fluoroalkene 1,1,1-trifluoropropene (HFO-1243zf) are each flammable and therefore not viable for use in many applications.
  • Higher fluoroalkenes, that is fluorine-substituted alkenes having at least five carbon atoms, have been suggested for use as refrigerants. Smutry, U.S. Pat. No. 4,788,352 is directed to production of fluorinated C5 to C8 compounds having at least some degree of unsaturation. The Smutny patent identifies such higher olefins as being known to have utility as refrigerants, pesticides, dielectric fluids, heat transfer fluids, solvents, and intermediates in various chemical reactions.
  • While the fluorinated olefins described in Smutny may have some level of effectiveness in heat transfer applications, it is believed that such compounds may also have certain disadvantages. For example, some of these compounds may tend to attack substrates, particularly general-purpose plastics such as acrylic resins and ABS resins. Furthermore, the higher olefinic compounds described in Smutny may also be undesirable in certain applications because of the potential level of toxicity of such compounds which may arise as a result of pesticide activity noted in Smutny. Also, such compounds may have a boiling point which is too high to make them useful as a refrigerant in certain applications.
  • Applicant have thus come to appreciate a need for compositions, and particularly fluid transfer compositions that are potentially useful in numerous applications, including vapor compression heating and cooling systems and methods, while avoiding one or more of the disadvantages noted above. Moreover, applicant has also recognized that in many applications there remains a need for fluorocarbon and hydrofluorocarbon-based refrigeration liquids that are environmentally safer than HFC's, possess similar or better characteristics with respect to at least certain refrigerant thermodynamic performance properties, and are compatible with existing lubricant systems.
  • SUMMARY
  • Applicants have found that the above-noted needs, and other needs, can be satisfied by compositions comprising one or more C3 or C4 fluoroalkenes, preferably compounds having Formula I as follows:

  • XCFZR3-Z  (I)
  • where X is a C2 or a C3 unsaturated, substituted or unsubstituted, alkyl radical, R is independently Cl, Br, I or H, and z is 1 to 3. The present compositions also preferably include one or more lubricants in combination with one or more of the compounds of the present invention.
  • The present invention provides also methods and systems which utilize the heat transfer compositions of the present invention.
  • DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
  • The Compositions
  • The present invention is directed to compositions comprising at least one fluoroalkene containing from 3 to 4 carbon atoms and at least one carbon-carbon double bond. The fluoroalkene compounds of the present invention are sometimes referred to herein for the purpose of convenience as hydrofluoro-olefins or “HFOs.” Although it is contemplated that the HFOs of the present invention may contain two carbon-carbon double bonds, such compounds at the present time are not considered to be preferred.
  • As mentioned above, the present compositions comprise one or compounds in accordance with Formula I. In preferred embodiments, the compositions include compounds of Formula II below:
  • Figure US20170233624A1-20170817-C00001
  • wherein each R is independently Cl, F, Br, I or H; R′ is (CR2)nY; Y is CRF2 and n is 0 or 1. In highly preferred embodiments, Y is CF3, n is 0 and at least one of the remaining R's is F.
  • Applicant believes that, in general, the compounds of the above identified Formulas I and II are generally effective and exhibit utility in heat transfer applications in general and in compression refrigerant compositions in particular. However, it has been surprisingly and unexpectedly found that certain of the compounds having a structure in accordance with the formulas described above exhibit a highly desirable low level of toxicity compared to other of such compounds. As can be readily appreciated, this discovery is of potentially enormous advantage and benefit for the formulation of not only refrigerant compositions, but also any and all compositions which would otherwise contain relatively toxic compounds satisfying the formulas described above. More particularly, it is believed that a relatively low toxicity level is associated with compounds of Formula II, preferably wherein Y is CF3, wherein at least one R on the unsaturated terminal carbon is H, and at least one of the remaining R's is F. It is believed also that all structural, geometric and stereoisomers of such compounds are effective and of beneficially low toxicity.
  • In highly preferred embodiments, especially embodiments which comprise the low toxicity compounds described above, n is zero. Thus, in certain preferred embodiments the compositions of the present invention comprise one or more compounds selected from the group consisting of trifluoropropene (HFC-1243), tetra-fluoropropenes (HFO-1234), pentafluoropropenes (HFO-1225) and combinations of these. The trans-1234 isomer has a boiling point of approximately −19° C. and the cis isomer has a boiling point of approximately +9° C. The trans isomer is particularly useful as a refrigerant and as an aersol propellent.
  • It is even more preferred that the compounds of the present invention are the tetrafluoropropene and pentafluoropropene compounds in which the unsaturated terminal carbon has not more than one F substituent, specifically: 1,3,3,3-tetrafluoropropene (HFO-1234ze); 2,3,3,3-tetrafluoropropene (HFO-1234yf); and 1,2,3,3,3-pentafluoropropene (HFO-1225ye), and any and all stereoisomers of each of these. It has been discovered that such compounds have a very acute low toxicity level, as measured by inhalation exposure to mice and rats. On the other hand, it has been found that a relatively high degree of toxicity may be associated with certain compounds adaptable for use with the present compositions, namely, those compounds which have more than one F on the terminal unsaturated carbon, or which do not have at least one H on the terminal unsaturated carbon. For example, it has been discovered that 1,1,3,3,3-pentafluoropropene (HFO-1225zc) exhibits an unacceptably high degree of toxicity, as measured by inhalation exposure to mice and rats.
  • The preferred compounds of the present invention, namely, HFO-1225 and HFO-1234 are known materials and are listed in Chemical Abstracts databases. HFO-1225 is commercially available, for example from Syntex Chemical Co. Furthermore, methods are described generally in the patent literature for producing fluoroalkenes. For example the production of fluoropropenes such as CF3CH═CH2 by catalytic vapor phase fluorination of various saturated and unsaturated halogen-containing C3 compounds is described in U.S. Pat. Nos. 2,889,379; 4,798,818 and 4,465,786, each of which is incorporated herein by reference. U.S. Pat. No. 5,532,419, which is also incorporated herein by reference, discloses a vapor phase catalytic process for the preparation of fluoroalkene using a chloro- or bromo-halofluorocarbon and H. EP 974,571, also incorporated herein by reference, discloses the preparation of 1,1,1,3-tetrafluoro-propene by contacting 1,1,1,3,3-pentafluoropropane (HFC-245fa) in the vapor phase with a chromium-based catalyst at elevated temperature, or in the liquid phase with an alcoholic solution of KOH, NaOH, Ca(OH)2 or Mg(OH)2. In addition, methods for producing compounds in accordance with the present invention are described generally in connection with concurrently filed United States Patent Application entitled “Process for Producing Fluorpropenes” bearing attorney docket number (H0003789 (26,267USA)), which is also incorporated herein by reference.
  • The present compositions are believed to possess properties that are advantageous for a number of important reasons. For example, applicants believe, based at least in part on mathematical modeling, that the fluoroolefins of the present invention will not have a substantial negative affect on atmospheric chemistry, being negligible contributors to ozone depletion in comparison to some other halogenated species. The preferred compositions of the present invention thus have the advantage of not contributing substantially to ozone depletion. The preferred compositions also do not contribute substantially to global warming compared to many of the hydrofluoroalkanes presently in use.
  • Although it is contemplated that the compositions of the present invention may include the compounds of the present invention in widely ranging amounts, it is generally preferred that refrigerant compositions of the present invention comprise compound(s) in accordance with Formula I, and even more preferably Formula II, in an amount that is at least about 50% by weight, and even more preferably at least about 70% by weight, of the composition. For preferred compositions for use as blowing agents in accordance with the present invention, compound(s) in accordance with Formula I, and even more preferably Formula II, are present in an amount that is at least about 5% by weight, and even more preferably at least about 15% by weight, of the composition.
  • The compositions of the present invention may include other components for the purpose of enhancing or providing certain functionality to the composition, or in some cases to reduce the cost of the composition. For example, refrigerant compositions according to the present invention, especially those used in vapor compression systems, include a lubricant, generally in amounts of from about 30 to about 50 percent by weight of the composition. Furthermore, the present compositions may also include a compatibilizer, such as propane, for the purpose of aiding compatibility and/or solubility of the lubricant. Such compatibilizers, including propane, butanes and pentanes, are preferably present in amounts of from about 0.5 to about 5 percent by weight of the composition. Combinations of surfactants and solubilizing agents may also be added to the present compositions to aid oil solubility, as disclosed by U.S. Pat. No. 6,516,837, the disclosure of which is incorporated by reference. Commonly used refrigeration lubricants such as Polyol Esters (POEs), Poly Alkylene Glycols (PAGs) and esterified Poly Alkylene Glycols that are used in refrigeration machinery with hydrofluorocarbon (HFC) refrigerants may be used with the refrigerant compositions of the present invention.
  • Methods and Systems
  • The compositions of the present invention are useful in connection with numerous methods and systems, including as heat transfer fluids in methods and systems for transferring heat, such as refrigerants used in refrigeration, air conditioning and heat pump systems.
  • The preferred heat transfer methods generally comprise providing a composition of the present invention and causing heat to be transferred to or from the composition by changing the phase of the composition. For example, the present methods provide cooling by absorbing heat from a fluid or article, preferably by condensing a refrigerant comprising the present compositions and thereafter evaporating the refrigerant in the vicinity of the body or fluid to be cooled. In many of such processes, the step of compressing the refrigerant vapor, usually with a rotary compressor or similar equipment, is also included as part of the refrigeration cycle. Such a step is then sometimes followed by an intermediate cooling step to remove at least a portion of the heat added to the refrigerant composition of the present invention by the compression step. This intermediate cooling step is then preferably followed by a nominally isoenthalpic reduction of the pressure of the cooled, high pressure refrigerant vapor to cause at least a portion of the vapor to condense to a relatively cold liquid phase. In such embodiments, it is this reduced temperature refrigerant liquid which is then vaporized by heat transferred from the body or fluid to be cooled.
  • In another process embodiment of the invention, the compositions of the invention may be used in a method for producing heating which comprises condensing a refrigerant comprising the compositions in the vicinity of a liquid or body to be heated and thereafter evaporating the refrigerant. Such methods, as mentioned hereinbefore, frequently are reverse cycles to the refrigeration cycle described above.
  • According to one aspect of the present invention, a method for producing refrigeration is provided by condensing a fluoroalkene containing from 2 to 5 carbon atoms and at least 1 but no more than 2 double bonds and thereafter evaporating the fluoroalkene in the vicinity of a body to be cooled. Fluoroalkenes containing 3 carbon atoms and 1 double bond are preferred.
  • Because heat pump systems are simply the reverse of refrigeration systems, according to another aspect of the present invention, a method is provided for producing heating by condensing a fluoroalkene containing from 2 to 5 carbon atoms and at least 1 but no more than 2 double bonds in the vicinity of a body to be heated and thereby evaporating the fluoroalkene. Again, fluoroalkenes containing 3 carbon atoms and 1 double bond are preferred.
  • It has also been discovered that the fluoroalkenes of the present invention are misicible with existing polyalkylene glycol, polyalkylene glycol ester and polyol ester lubricating oils. Therefore, according to another aspect of the present invention, a liquid composition is provided for use in compression refrigeration, air-conditioning and heat pump systems in which a fluoroalkene containing from 2 to 5 carbon atoms and at least 1 but no more than 2 double bonds is combined with a sufficient amount to provide lubrication of an essentially miscible organic lubricant selected from polyalkylene glycol, polyalkylene glycol ester and polyol ester lubricants for compression refrigeration, air-conditioning and heat pump systems. In certain preferred embodiments, the lubricants of this invention are organic compounds which are comprised of carbon, hydrogen and oxygen with a ratio of oxygen to carbon sufficient to provide a degree of miscibility with the fluoroalkene such the when about 1 to 5 weight percent of the lubricant is added to the refrigerant fluid the mixture has one liquid phase. Preferably, the mixture has one liquid phase when 1 to 20 weight percent of the lubricant is present in the mixture. Most preferably, the mixture is one liquid phase in all proportions of the components of mixture. This solubility or miscibility preferably exists at least one temperature from about −40° C. and 70° C., and more preferably over essentially the entire temperature range.
  • As used herein the term “refrigeration system” refers to any system or apparatus, or any part or portion of such a system or apparatus, which employs a refrigeration liquid or refrigerant to provide cooling. Such refrigeration systems include, for example, air-conditioners, electric refrigerators, chillers, transport refrigeration systems, commercial refrigeration systems, and the like.
  • The present invention substitutes HFO's for HFC's, which, despite being safe for the ozone layer, are suspected of contributing to global warming. At least certain of the preferred HFO's according to the present invention have physical characteristics that allow for their substitution for HFC's with only a minimum of equipment changes.
  • The polyalkylene glycol lubricants suitable for use with the present invention typically containing from about 5 to 50 oxyalkylene repeating units that contain from 1 to 5 carbon atoms. The polyalkylene glycol can be straight chain or branched and can be a homopolymer or co-polymer of 2, 3 or more oxyethylene, oxypropylene, oxybutylene or oxypentylene groups or combinations thereof in any proportions. Preferred polyalkylene glycols contain at least 50% oxypropylene groups. Compositions according to the present invention may contain one or more polyalkylene glycols as the lubricant, one or more polyalkylene glycol esters as the lubricant, one or more polyol esters as the lubricant, or a mixture of one of more polyalkylene glycols, one or more polyalkylene glycol esters and one or more polyol esters. Vinyl ethers are also useful in this invention.
  • Suitable polyalkylene glycols include the polyalkylene glycols of U.S. Pat. No. 4,971,712 and the polyalkylene glycol having hydroxy groups at each terminus disclosed by U.S. Pat. No. 4,755,316. The disclosures of both patents are incorporated herein by reference.
  • While suitable polyalkylene glycols include glycols terminating at each end with a hydroxyl group, other suitable HFO lubricants include polyalkylene glycols in which either or both terminal hydroxyl group is capped. The hydroxyl group may be capped with alkyl groups containing from 1 to 10 carbon atoms, 1 to 10 carbon atom alkyl groups containing heteroatoms such as nitrogen, the fluoroalkyl groups described by U.S. Pat. No. 4,975,212, the disclosure of which is incorporated herein by reference, and the like. When both polyalkylene glycol hydroxyl groups are end capped, the same type or a combination of two different types of terminal capping groups can be used.
  • Either or both hydroxyl groups can also be capped by forming the ester thereof with a carboxylic acid as disclosed by U.S. Pat. No. 5,008,028, the disclosure of which is also incorporated herein by reference. The lubricating oils of this patent are referred to as polyol esters and polyalkylene glycol esters. The carboxylic acid can also be fluorinated. When both ends of the polyalkylene glycol are capped, either or both ends may be capped with an ester, or one end may be capped with an ester and the other not capped or capped with one of the aforementioned alkyl, heteroalkyl or fluoroalkyl groups.
  • Commercially available polyalkylene glycol lubricants include Goodwrench Refrigeration Oil for HFC-134a systems from General Motors and MOPAR-56 from Daimler-Chrysler, which is a polyalkylene glycol that is bis-capped by acetyl groups. Commercially available polyalkylene glycol esters include Mobil EAL 22 cc available from Exxon-Mobil and Solest 120 available from CPI Engineering Services, Inc. A wide variety of polyalkylene glycol lubricants are also available from Dow Chemical.
  • In preferred embodiments, the lubricants of this invention have viscosities of from about 1 to 1000 centistokes at about 37° C., more preferably in the range of from about 10 to about 200 centistokes at about 37° C. and even more preferably of from about 30 to about 150 centistokes.
  • In addition to the HFO refrigerant and lubricant, compositions according to the present invention can include other additives or materials of the type used in refrigeration, air-conditioning and heat pump compositions to enhance their performance. For example, the compositions can also include extreme pressure and anti-wear additives, oxidation and thermal stability improvers, pour and floc point depressants, anti-foaming agents, other lubricants soluble in HFO's, and the like. Examples of such additives are disclosed in U.S. Pat. No. 5,254,280, the disclosure of which is incorporated herein by reference. Compositions of the present invention can thus further include a quantity of mineral oil lubricant that would not otherwise be misicible or soluble with the HFO but is at least partially misicible or partially soluble when added to the HFO in combination with a polyalkylene glycol, polyalkylene glycol ester or polyol ester. Typically, this is a quantity up to about 5-20 weight %. A surfactant may also be added to compatibilize the mineral oil with the polyalkylene glycol, polyalkylene glycol ester or polyol ester and the HFO, as disclosed in U.S. Pat. No. 6,516,837, the disclosure of which is incorporated herein by reference.
  • Any of a wide range of methods for introducing the refrigeration compositions of the present invention to a compression refrigeration, air-conditioning or heat pump system can be used from the present invention. For example, one method comprises attaching a refrigerant container to the low-pressure side of a refrigeration system and turning on the refrigeration system compressor to pull the refrigeration composition into the system. In such embodiments, the refrigerant container may be placed on a scale such that the amount of refrigeration composition entering the system can be monitored. When a desired amount of refrigeration composition has been introduced into the system, charging is stopped. Alternatively, a wide range of charging tools, known to those skilled in the art, are commercially available. Accordingly, in light of the above disclosure, those of skill in the art will be readily able to introduce the HFO refrigerant and refrigeration compositions of the present invention into compression refrigeration, air-conditioning and heat pump systems without undue experimentation.
  • EXAMPLES
  • The following examples are provided for the purpose of illustrating the present invention but without limiting the scope thereof.
  • Example 1
  • The coefficient of performance (COP) is a universally accepted measure of refrigerant performance, especially useful in representing the relative thermodynamic efficiency of a refrigerant in a specific heating or cooling cycle involving evaporation or condensation of the refrigerant. In refrigeration engineering, this term expresses the ratio of useful refrigeration to the energy applied by the compressor in compressing the vapor. The capacity of a refrigerant represents the volumetric efficiency of the refrigerant and provides some measure of the capability of a compressor to pump quantities of heat for a given volumetric flow rate of refrigerant. In other words, given a specific compressor, a refrigerant with a higher capacity will deliver more cooling or heating power. One means for estimating COP of a refrigerant at specific operating conditions is from the thermodynamic properties of the refrigerant using standard refrigeration cycle analysis techniques (see for example, R. C. Downing, FLUOROCARBON REFRIGERANTS HANDBOOK, Chapter 3, Prentice-Hall, 1988).
  • A refrigeration/air conditioning cycle system is provided where the condenser temperature is about 150° F. and the evaporator temperature is about −35° F. under nominally isoentropic compression with a compressor inlet temperature of about 50° F. COP is determined for several compositions of the present invention over a range of condenser and evaporator temperatures and reported in Table I below, based upon HFC-134a having a COP value of 1.00, a capacity value of 1.00 and a discharge temperature of 175° F.
  • TABLE I
    DISCHARGE
    REFRIGERANT Relative Relative TEMPERATURE
    COMPOSTION COP CAPACITY (° F.)
    HFO 1225ye 1.02 0.76 158
    HFO trans-1234ze 1.04 0.70 165
    HFO cis-1234ze 1.13 0.36 155
    HFO 1234yf 0.98 1.10 168
  • This example shows that certain of the preferred compounds for use with the present compositions each have a better energy efficiency than HFC-134a (1.02, 1.04 and 1.13 compared to 1.00) and the compressor using the present refrigerant compositions will produce discharge temperatures (158, 165 and 155 compared to 175), which is advantageous since such result will likely leading to reduced maintenance problems.
  • Example 2
  • The miscibility of HFO-1225ye and HFO-1234ze with various refrigeration lubricants is tested. The lubricants tested are mineral oil (C3), alkyl benzene (Zerol 150), ester oil (Mobil EAL 22 cc and Solest 120), polyalkylene glycol (PAG) oil (Goodwrench Refrigeration Oil for 134a systems), and a poly(alpha-olefin) oil (CP-6005-100). For each refrigerant/oil combination, three compositions are tested, namely 5, 20 and 50 weight percent of lubricant, with the balance of each being the compound of the present invention being tested
  • The lubricant compositions are placed in heavy-walled glass tubes. The tubes are evacuated, the refrigerant compound in accordance with the present invention is added, and the tubes are then sealed. The tubes are then put into an air bath environmental chamber, the temperature of which is varied from about −50° C. to 70° C. At roughly 10° C. intervals, visual observations of the tube contents are made for the existence of one or more liquid phases. In a case where more than one liquid phase is observed, the mixture is reported to be immiscible. In a case where there is only one liquid phase observed, the mixture is reported to be miscible. In those cases where two liquid phases were observed, but with one of the liquid phases occupying only a very small volume, the mixture is reported to be partially miscible.
  • The polyalkylene glycol and ester oil lubricants were judged to be miscible in all tested proportions over the entire temperature range, except that for the HFO-1225ye mixtures with polyalkylene glycol, the refrigerant mixture was found to be immiscible over the temperature range of −50° C. to −30° C. and to be partially miscible over from −20 to 50° C. At 50 weight percent concentration of the PAG in refrigerant and at 60°, the refrigerant/PAG mixture was miscible. At 70° C., it was miscible from 5 weight percent lubricant in refrigerant to 50 weight percent lubricant in refrigerant.
  • Example 3
  • The compatibility of the refrigerant compounds and compositions of the present invention with PAG lubricating oils while in contact with metals used in refrigeration and air conditioning systems is tested at 350° C., representing conditions much more severe than are found in many refrigeration and air conditioning applications.
  • Aluminum, copper and steel coupons are added to heavy walled glass tubes. Two grams of oil are added to the tubes. The tubes are then evacuated and one gram of refrigerant is added. The tubes are put into an oven at 350° F. for one week and visual observations are made. At the end of the exposure period, the tubes are removed.
  • This procedure was done for the following combinations of oil and the compound of the present invention:
  • a) HFC-1234ze and GM Goodwrench PAG oil
  • b) HFC1243zf and GM Goodwrench oil PAG oil
  • c) HFC-1234ze and MOPAR-56 PAG oil
  • d) HFC-1243zf and MOPAR-56 PAG oil
  • e) HFC-1225 ye and MOPAR-56 PAG oil.
  • In all cases, there is minimal change in the appearance of the contents of the tube. This indicates that the refrigerant compounds and compositions of the present invention are stable in contact with aluminum, steel and copper found in refrigeration and air conditioning systems, and the types of lubricating oils that are likely to be included in such compositions or used with such compositions in these types of systems.
  • Comparative Example
  • Aluminum, copper and steel coupons are added to a heavy walled glass tube with mineral oil and CFC-12 and heated for one week at 350° C., as in Example 3. At the end of the exposure period, the tube is removed and visual observations are made. The liquid contents are observed to turn black, indicating there is severe decomposition of the contents of the tube.
  • CFC-12 and mineral oil have heretofore been the combination of choice in many refrigerant systems and methods. Thus, the refrigerant compounds and compositions of the present invention possess significantly better stability with many commonly used lubricating oils than the widely-used prior art refrigerant-lubricating oil combination.

Claims (42)

What is claimed is:
1. A liquid composition for use in compression refrigeration, air-conditioning and heat pump systems comprising:
(A) a fluoroalkene containing from 3 to 4 carbon atoms and at least 1 but no more than 2 double bonds; and
(B) an effective amount to provide lubrication of an essentially miscible organic lubricant comprised of carbon, hydrogen and oxygen and having a ratio of oxygen to carbon effective to provide a degree of miscibility with said fluoroalkene so that when up to five weight percent of lubricant is added to said fluoroalkene the mixture has one liquid phase at least one temperature between −40 and +70° C.
2. The composition of claim 1, wherein the mixture has one liquid phase when up to five weight percent of lubricant is added to said fluoroalkene.
3. The composition of claim 2, wherein the mixture has one liquid phase when up to 20 weight percent of lubricant is added to said fluoroalkene.
4. The composition of claim 3, wherein the mixture has one liquid phase in all proportions of fluoroalkene and lubricant.
5. The composition of claim 1, wherein the mixture has one liquid phase over essentially the entire temperature range.
6. The composition of claim 1, wherein said lubricant is selected from the group consisting of polyalkylene glycol, polyalkylene glycol ester and polyol ester lubricants for compressor refrigeration, air-conditioning and heat pump systems.
7. The composition of claim 1, wherein said fluoroalkene has the structure:

XCFZR3-Z
wherein X is a C2 or a C3 unsaturated, substituted or unsubstituted alkyl radical, R is independently selected from the group consisting of Cl, Br, I or H, and z is 1 to 3.
8. The composition of claim 7, wherein said fluoroalkene has the structure:
Figure US20170233624A1-20170817-C00002
wherein each R is independently Cl, F, Br, I or H; R′ is (CR2)nY; Y is CRF2; and n is 0 or 1.
9. The composition of claim 8, wherein said fluoroalkene is 1,3,3,3-tetrafluoro-propene or 3,3,3-trifluoropropene.
10. The composition of claim 1, wherein said organic lubricant is a polyalkylene glycol.
11. The composition of claim 10, wherein said polyalkylene glycol has at least one terminal hydroxyl group.
12. The composition of claim 11, wherein both terminal groups of said polyalkylene glycol are hydroxyl groups.
13. The composition of claim 10, wherein said polyalkylene glycol has at least one alkyl terminal group.
14. The composition of claim 13, wherein at least one terminal alkyl group of said polyalkylene glycol contains at least one heteroatom.
15. The composition of claim 14, wherein said polyalkylene glycol has at least one fluoroalkyl terminal group.
16. The composition of claim 1, wherein said organic lubricant is a polyalkylene glycol ester.
17. The composition of claim 1, further comprising an amount of hydrocarbon lubricant essentially miscible with said fluoroalkene and said organic lubricant.
18. The composition of claim 17, further comprising a surfactant for solubilizing said hydrocarbon lubricant with said organic lubricant, in an amount effective to form an essentially miscible blend.
19. A method for producing refrigeration which comprises condensing a refrigerant composition comprising a fluoroalkene containing from 3 to 4 carbon atoms and at least 1 but no more than 2 double bonds, and thereafter evaporating said refrigerant composition in the vicinity of a body to be cooled.
20. The method of claim 19, wherein said fluoroalkene has the structure:

XCFZR3-Z
wherein X is a C2 or a C3 unsaturated, substituted or unsubstituted alkyl radical, R is independently selected from the group consisting of Cl, Br, I or H, and z is 1 to 3.
21. The method of claim 20, wherein said fluoroalkene has the structure:
Figure US20170233624A1-20170817-C00003
wherein each R is independently Cl, F, Br, I or H; R′ is (CR2)nY; Y is CRF2; and n is 0 or 1.
22. The method of claim 21, wherein said fluoroalkene is 1,3,3,3-tetrafluoropropene or 3,3,3-trifluoropropene.
23. The method of claim 19, wherein said refrigeration method is performed in a compression refrigeration system.
24. The method of claim 19, wherein said refrigeration method is performed in an air-conditioning system.
25. The method of claim 19, wherein an organic lubricant is added to said refrigerant in an amount effective to provide lubrication comprised of carbon, hydrogen and oxygen and having a ratio of oxygen to carbon effective to provide a degree of miscibility with said fluoroalkene so that when up to five weight percent of lubricant is added to said fluoroalkene the refrigerant has one liquid phase at least one temperature between −40 and +70° C.
26. The method of claim 25, wherein the refrigerant has one liquid phase when up to 20 weight percent of lubricant is added to said fluoroalkene.
27. The method of claim 26, wherein the refrigerant has one liquid phase in all proportions of fluoroalkene and lubricant.
28. The method of claim 25, wherein the refrigerant has one liquid phase over essentially the entire temperature range.
29. The method of claim 25, wherein said lubricant is selected from the group consisting of polyalkylene glycol, polyalkylene glycol ester and polyol ester lubricants for compressor refrigeration and air-conditioning systems.
30. The method of claim 25, wherein there is further added to said refrigerant an amount of a hydrocarbon lubricant essentially miscible with said fluoroalkene and said organic lubricant.
31. The method of claim 30, wherein there is further added to said refrigerant a surfactant for solubilizing said hydrocarbon lubricant with said fluoroalkene and said organic lubricant in an amount effective to form an essentially miscible blend.
32. A method for producing heating which comprises condensing a fluoroalkene composition containing from 3 to 4 carbon atoms and at least 1 but no more than 2 double bonds in the vicinity of a body to be heated and thereafter evaporating said fluoroalkene composition.
33. The method of claim 32, wherein said fluoroalkene has the structure:

XCFZR3-Z
wherein X is a C2 or a C3 unsaturated, substituted or unsubstituted alkyl radical, R is independently selected from the group consisting of Cl, Br, I or H, and z is 1 to 3.
34. The method of claim 33, wherein said fluoroalkene has the structure:
Figure US20170233624A1-20170817-C00004
wherein each R is independently Cl, F, Br, I or H; R′ is (CR2)nY; Y is CRF2; and n is 0 or 1.
35. The method of claim 34, wherein said fluoroalkene is 1,3,3,3-tetrafluoropropene or 3,3,3-trifluoropropene.
36. The method of claim 32, wherein an organic lubricant is added to said fluoroalkene composition in an amount effective to provide lubrication comprised of carbon, hydrogen and oxygen and having a ratio of oxygen to carbon effective to provide a degree of miscibility with said fluoroalkene composition so that when up to five weight percent of lubricant is added to said fluoroalkene composition, said composition has one liquid phase at least one temperature between −40 and +70° C.
37. The method of claim 36, wherein the fluoroalkene composition has one liquid phase when up to 20 weight percent of lubricant is added thereto.
38. The method of claim 37, wherein the fluoroalkene composition has one liquid phase in all proportions of fluoroalkene composition and lubricant.
39. The method of claim 36, wherein the fluoroalkene composition has one liquid phase over essentially the entire temperature range.
40. The method of claim 36, wherein said lubricant is selected from the group consisting of polyalkylene glycol, polyalkylene glycol ester and polyol ester lubricants for compressor refrigeration and air-conditioning systems.
41. The method of claim 36, wherein there is further added to said fluoroalkene composition an amount of a hydrocarbon lubricant essentially miscible with said fluoroalkene and said organic lubricant.
42. The method of claim 41, wherein there is further added to said fluoroalkene composition a surfactant for solubilizing said hydrocarbon lubricant with said fluoroalkene and said organic lubricant in an amount effective to form an essentially miscible blend.
US15/389,697 2002-10-25 2016-12-23 Fluorinated alkene refrigerant compositions Abandoned US20170233624A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US15/389,697 US20170233624A1 (en) 2002-10-25 2016-12-23 Fluorinated alkene refrigerant compositions

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US42126302P 2002-10-25 2002-10-25
US42143502P 2002-10-25 2002-10-25
US10/695,212 US20040089839A1 (en) 2002-10-25 2003-10-27 Fluorinated alkene refrigerant compositions
US11/385,259 US9631129B2 (en) 2002-10-25 2006-03-20 Fluorinated alkene refrigerant compositions
US15/389,697 US20170233624A1 (en) 2002-10-25 2016-12-23 Fluorinated alkene refrigerant compositions

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US11/385,259 Division US9631129B2 (en) 2002-10-25 2006-03-20 Fluorinated alkene refrigerant compositions

Publications (1)

Publication Number Publication Date
US20170233624A1 true US20170233624A1 (en) 2017-08-17

Family

ID=34549972

Family Applications (5)

Application Number Title Priority Date Filing Date
US10/695,212 Abandoned US20040089839A1 (en) 2002-10-25 2003-10-27 Fluorinated alkene refrigerant compositions
US11/385,259 Expired - Lifetime US9631129B2 (en) 2002-10-25 2006-03-20 Fluorinated alkene refrigerant compositions
US15/389,697 Abandoned US20170233624A1 (en) 2002-10-25 2016-12-23 Fluorinated alkene refrigerant compositions
US15/490,413 Abandoned US20180094179A1 (en) 2002-10-25 2017-04-18 Fluorinated alkene refrigerant compositions
US16/589,770 Abandoned US20200208034A1 (en) 2002-10-25 2019-10-01 Fluorinated alkene refrigerant compositions

Family Applications Before (2)

Application Number Title Priority Date Filing Date
US10/695,212 Abandoned US20040089839A1 (en) 2002-10-25 2003-10-27 Fluorinated alkene refrigerant compositions
US11/385,259 Expired - Lifetime US9631129B2 (en) 2002-10-25 2006-03-20 Fluorinated alkene refrigerant compositions

Family Applications After (2)

Application Number Title Priority Date Filing Date
US15/490,413 Abandoned US20180094179A1 (en) 2002-10-25 2017-04-18 Fluorinated alkene refrigerant compositions
US16/589,770 Abandoned US20200208034A1 (en) 2002-10-25 2019-10-01 Fluorinated alkene refrigerant compositions

Country Status (14)

Country Link
US (5) US20040089839A1 (en)
EP (6) EP2009075B1 (en)
JP (6) JP2007510039A (en)
KR (2) KR101335358B1 (en)
CN (5) CN103923723B (en)
DE (1) DE08011766T1 (en)
DK (3) DK1725628T3 (en)
ES (5) ES2628746T3 (en)
HU (2) HUE032542T2 (en)
PL (5) PL2275509T3 (en)
PT (4) PT2275509T (en)
SI (3) SI2277976T1 (en)
TR (1) TR201708747T4 (en)
WO (1) WO2005042663A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9919939B2 (en) 2011-12-06 2018-03-20 Delta Faucet Company Ozone distribution in a faucet
US11458214B2 (en) 2015-12-21 2022-10-04 Delta Faucet Company Fluid delivery system including a disinfectant device

Families Citing this family (122)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050096246A1 (en) * 2003-11-04 2005-05-05 Johnson Robert C. Solvent compositions containing chlorofluoroolefins
US20040089839A1 (en) 2002-10-25 2004-05-13 Honeywell International, Inc. Fluorinated alkene refrigerant compositions
US7279451B2 (en) 2002-10-25 2007-10-09 Honeywell International Inc. Compositions containing fluorine substituted olefins
US7833433B2 (en) * 2002-10-25 2010-11-16 Honeywell International Inc. Heat transfer methods using heat transfer compositions containing trifluoromonochloropropene
US9994750B2 (en) * 2002-10-25 2018-06-12 Honeywell International Inc. Compositions containing fluorine substituted olefins and methods and systems using same
EP2277942A3 (en) 2002-10-25 2014-07-09 Honeywell International, Incorporated. Compositions containing fluorine substituted olefins
US8033120B2 (en) 2002-10-25 2011-10-11 Honeywell International Inc. Compositions and methods containing fluorine substituted olefins
US7655610B2 (en) 2004-04-29 2010-02-02 Honeywell International Inc. Blowing agent compositions comprising fluorinated olefins and carbon dioxide
US7524805B2 (en) 2004-04-29 2009-04-28 Honeywell International Inc. Azeotrope-like compositions of tetrafluoropropene and hydrofluorocarbons
US9499729B2 (en) 2006-06-26 2016-11-22 Honeywell International Inc. Compositions and methods containing fluorine substituted olefins
US8008244B2 (en) 2004-04-29 2011-08-30 Honeywell International Inc. Compositions of tetrafluoropropene and hydrocarbons
US20220389297A1 (en) 2005-03-04 2022-12-08 The Chemours Company Fc, Llc Compositions comprising a fluoroolefin
US7569170B2 (en) 2005-03-04 2009-08-04 E.I. Du Pont De Nemours And Company Compositions comprising a fluoroolefin
US20060243944A1 (en) * 2005-03-04 2006-11-02 Minor Barbara H Compositions comprising a fluoroolefin
EP3351609B1 (en) * 2005-03-04 2020-08-26 The Chemours Company FC, LLC Method for replacing a high gwp refrigerant by compositions comprising hfc-1234yf
US8574451B2 (en) * 2005-06-24 2013-11-05 Honeywell International Inc. Trans-chloro-3,3,3-trifluoropropene for use in chiller applications
TWI558685B (en) * 2005-06-24 2016-11-21 哈尼威爾國際公司 Compositions containing fluorine substituted olefins
US7708903B2 (en) 2005-11-01 2010-05-04 E.I. Du Pont De Nemours And Company Compositions comprising fluoroolefins and uses thereof
WO2007053697A2 (en) * 2005-11-01 2007-05-10 E. I. Du Pont De Nemours And Company Compositions comprising fluoroolefins and uses thereof
ES2829325T3 (en) * 2005-11-01 2021-05-31 Chemours Co Fc Llc Compositions comprising 1,1,1,4,4,4-hexafluoro-2-butene and uses thereof
US20070210276A1 (en) * 2006-03-10 2007-09-13 Honeywell International Inc. Method for generating pollution credits
CA2646990C (en) * 2006-03-21 2018-02-20 Honeywell International Inc. Foaming agents containing fluorine substituted unsaturated olefins
GB0611742D0 (en) 2006-06-14 2006-07-26 Ineos Fluor Holdings Ltd Desiccants for fluids
ES2539939T3 (en) * 2006-06-27 2015-07-07 E.I. Du Pont De Nemours And Company Production procedures of 1,2,3,3,3-pentafluoropropene
KR20090027771A (en) * 2006-07-12 2009-03-17 솔베이 플루오르 게엠베하 Method for heating and cooling using fluoroether compounds, compositions suitable therefore and their use
CN101827912A (en) * 2006-09-01 2010-09-08 纳幕尔杜邦公司 Method for circulating selected heat transfer fluids through a closed loop cycle
CN101522849B (en) * 2006-09-01 2014-05-07 纳幕尔杜邦公司 Phosphorus-containing stabilizers for fluoroolefins
JP5139665B2 (en) 2006-11-02 2013-02-06 出光興産株式会社 Lubricating oil composition for refrigerator
JP5914912B2 (en) * 2007-02-27 2016-05-11 Jxエネルギー株式会社 Refrigerator oil and working fluid composition for refrigerator
JP2009074018A (en) * 2007-02-27 2009-04-09 Nippon Oil Corp Refrigerator oil and working fluid composition for refrigerator
RU2454453C2 (en) * 2007-02-27 2012-06-27 Ниппон Ойл Корпорейшн Refrigerator oil and refrigerator hydraulic fluid composition
JP5572284B2 (en) 2007-02-27 2014-08-13 Jx日鉱日石エネルギー株式会社 Refrigerator oil and working fluid composition for refrigerator
WO2008108365A1 (en) * 2007-03-08 2008-09-12 Idemitsu Kosan Co., Ltd. Lubricant for compression type refrigerating machine and refrigeration system using the same
JP5193485B2 (en) * 2007-03-27 2013-05-08 Jx日鉱日石エネルギー株式会社 Refrigerator oil and working fluid composition for refrigerator
CA2681602C (en) 2007-03-29 2014-10-28 Arkema Inc. Hydrofluoropropene blowing agents for thermoplastics
CN106281575A (en) * 2007-04-18 2017-01-04 出光兴产株式会社 Lubricating oil composition for refrigerator and compressor using the same
JP5226242B2 (en) * 2007-04-18 2013-07-03 出光興産株式会社 Lubricating oil composition for refrigerator
JP2008267251A (en) * 2007-04-19 2008-11-06 Sanden Corp Compressor
JP2010526982A (en) * 2007-05-11 2010-08-05 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Heat exchange method in a vapor compression heat transfer system and a vapor compression heat exchange system including an intermediate heat exchanger using a double row evaporator or double row condenser
US8460571B2 (en) * 2007-06-12 2013-06-11 Idemitsu Kosan Co., Ltd. Lubricant composition for refrigerator and compressor using the same
JP5599706B2 (en) * 2007-06-27 2014-10-01 アーケマ・インコーポレイテッド Stabilized hydrochlorofluoroolefins and hydrofluoroolefins
US9523026B2 (en) 2007-06-27 2016-12-20 Arkema Inc. Stabilized hydrochlorofluoroolefins and hydrofluoroolefins
CN101765648A (en) * 2007-07-27 2010-06-30 纳幕尔杜邦公司 compositions comprising fluoroolefins and uses thereof
US8512591B2 (en) 2007-10-12 2013-08-20 Mexichem Amanco Holding S.A. De C.V. Heat transfer compositions
US8628681B2 (en) 2007-10-12 2014-01-14 Mexichem Amanco Holding S.A. De C.V. Heat transfer compositions
US8333901B2 (en) 2007-10-12 2012-12-18 Mexichem Amanco Holding S.A. De C.V. Heat transfer compositions
GB201002625D0 (en) * 2010-02-16 2010-03-31 Ineos Fluor Holdings Ltd Heat transfer compositions
US20100282999A1 (en) * 2007-10-29 2010-11-11 Nippon Oil Corporation Refrigerator oil and working fluid composition for refrigerating machine
JP5241261B2 (en) 2008-02-15 2013-07-17 出光興産株式会社 Lubricating oil composition for refrigerator
JP5241263B2 (en) * 2008-02-15 2013-07-17 出光興産株式会社 Lubricating oil composition for refrigerator
JP5241262B2 (en) * 2008-02-15 2013-07-17 出光興産株式会社 Lubricating oil composition for refrigerator
JP4665976B2 (en) * 2008-02-22 2011-04-06 株式会社デンソー Refrigeration cycle equipment for vehicles
US20110001080A1 (en) 2008-03-07 2011-01-06 Arkema Inc. Stable formulated systems with chloro-3,3,3-trifluoropropene
JP5612250B2 (en) * 2008-03-07 2014-10-22 出光興産株式会社 Lubricating oil composition for refrigerator
JP2009222032A (en) 2008-03-18 2009-10-01 Daikin Ind Ltd Refrigerating apparatus
JP2009222360A (en) * 2008-03-18 2009-10-01 Daikin Ind Ltd Heat exchanger
JP5285765B2 (en) * 2008-04-01 2013-09-11 ハネウェル・インターナショナル・インコーポレーテッド How to select a lubricant for a heat pump
US9994751B2 (en) * 2008-04-30 2018-06-12 Honeywell International Inc. Absorption refrigeration cycles using a LGWP refrigerant
US20110232306A1 (en) * 2008-04-30 2011-09-29 Honeywell International Inc. Absorption refrigeration cycles using a lgwp refrigerant
JP2011163565A (en) * 2008-06-09 2011-08-25 Mitsubishi Electric Corp Air conditioning device
JP5339788B2 (en) * 2008-06-13 2013-11-13 三菱電機株式会社 Compressor and refrigeration cycle equipment
EP2312163A4 (en) * 2008-06-16 2015-06-17 Mitsubishi Electric Corp Scroll compressor
EP3081879B1 (en) * 2008-06-16 2021-05-12 Mitsubishi Electric Corporation Refrigeration cycle apparatus
JP5294719B2 (en) * 2008-06-17 2013-09-18 三菱電機株式会社 Rotary compressor
WO2009157325A1 (en) * 2008-06-24 2009-12-30 三菱電機株式会社 Refrigerating cycle apparatus, and air-conditioning apparatus
US8820079B2 (en) * 2008-12-05 2014-09-02 Honeywell International Inc. Chloro- and bromo-fluoro olefin compounds useful as organic rankine cycle working fluids
FR2936806B1 (en) 2008-10-08 2012-08-31 Arkema France REFRIGERANT FLUID
FR2937906B1 (en) * 2008-11-03 2010-11-19 Arkema France METHOD FOR HEATING AND / OR AIR CONDITIONING A VEHICLE
US20100122545A1 (en) 2008-11-19 2010-05-20 E. I. Du Pont De Nemours And Company Tetrafluoropropene compositions and uses thereof
US8871112B2 (en) * 2008-11-19 2014-10-28 E I Du Pont De Nemours And Company Compositions comprising 2,3,3,3-tetrafluoropropene and hydrocarbons and uses thereof
JP2012513527A (en) * 2008-12-23 2012-06-14 シュリーブ ケミカル プロダクツ インコーポレーテッド Refrigerant lubricant composition
EP2396293A1 (en) * 2009-02-11 2011-12-21 Arkema France Azeotrope and azeotrope-like compositions of chlorotrifluoropropene and pentane
JP2011001897A (en) 2009-06-19 2011-01-06 Panasonic Corp Compressor
JP2011047329A (en) * 2009-08-27 2011-03-10 Panasonic Corp Rotary compressor
SI3812360T1 (en) 2009-09-09 2024-02-29 Honeywell International Inc. Monochlorotrifluoropropene compounds and compositions and methods using same
FR2950065B1 (en) 2009-09-11 2012-02-03 Arkema France BINARY REFRIGERANT FLUID
FR2950066B1 (en) 2009-09-11 2011-10-28 Arkema France LOW AND MEDIUM TEMPERATURE REFRIGERATION
WO2011034904A1 (en) 2009-09-16 2011-03-24 E. I. Du Pont De Nemours And Company Chiller apparatus containing trans-1,1,1,4,4,4-hexafluoro-2-butene and methods of producing cooling therein
JP6141019B2 (en) 2009-12-29 2017-06-07 アーケマ・インコーポレイテッド Method for selecting refrigerant-lubricant combination
GB201002622D0 (en) 2010-02-16 2010-03-31 Ineos Fluor Holdings Ltd Heat transfer compositions
FR2957083B1 (en) 2010-03-02 2015-12-11 Arkema France HEAT TRANSFER FLUID FOR CENTRIFUGAL COMPRESSOR
JP5546918B2 (en) * 2010-03-19 2014-07-09 Jx日鉱日石エネルギー株式会社 Refrigerator oil and working fluid composition for refrigerator
ES2698388T3 (en) * 2010-04-16 2019-02-04 Chemours Co Fc Llc Coolers containing a composition comprising 2,3,3,3-tetrafluoropropene and 1,1,1,2-tetrafluoroethane
FR2959997B1 (en) 2010-05-11 2012-06-08 Arkema France HEAT TRANSFER FLUIDS AND THEIR USE IN COUNTER-CURRENT HEAT EXCHANGERS
FR2959999B1 (en) 2010-05-11 2012-07-20 Arkema France HEAT TRANSFER FLUIDS AND THEIR USE IN COUNTER-CURRENT HEAT EXCHANGERS
KR20130082096A (en) 2010-05-20 2013-07-18 멕시켐 아만코 홀딩 에스.에이. 데 씨.브이. Heat transfer compositions
PL2571952T3 (en) 2010-05-20 2016-01-29 Mexichem Fluor Sa De Cv Heat transfer compositions
GB2481443B (en) 2010-06-25 2012-10-17 Mexichem Amanco Holding Sa Heat transfer compositions
BR112013000242A2 (en) * 2010-07-06 2016-05-17 Arkema Inc tetrafluoropropene compositions and polyol ester lubricants
FR2964977B1 (en) 2010-09-20 2013-11-01 Arkema France COMPOSITION BASED ON 3,3,3-TETRAFLUOROPROPENE
FR2964976B1 (en) 2010-09-20 2012-08-24 Arkema France COMPOSITION BASED ON 1,3,3,3-TETRAFLUOROPROPENE
MY161767A (en) * 2010-12-14 2017-05-15 Du Pont Combinations of e-1,3,3,3-tetrafluoropropene and at least one tetrafluoroethane and their use for heating
IT1406472B1 (en) 2010-12-22 2014-02-28 Nuovo Pignone Spa TEST FOR SIMILITUDE OF COMPRESSOR PERFORMANCE
FR2971512B1 (en) 2011-02-10 2013-01-18 Arkema France BINARY COMPOSITIONS OF 2,3,3,3-TETRAFLUOROPROPENE AND AMMONIA
FR2974812B1 (en) * 2011-05-04 2014-08-08 Arkema France HEAT TRANSFER COMPOSITIONS HAVING IMPROVED MISCIBILITY WITH LUBRICATING OIL
US9187682B2 (en) 2011-06-24 2015-11-17 Emerson Climate Technologies, Inc. Refrigeration compressor lubricant
FR2977707B1 (en) 2011-07-05 2014-05-23 Schneider Electric Ind Sas USE OF HYDROFLUOROOLEFIN AS A MEDIUM VOLTAGE ARC INSULATION AND / OR EXTINGUISHMENT MEDIUM AND GAS INSULATED MEDIUM VOLTAGE ELECTRICAL APPARATUS COMPRISING SAME
CN105505325A (en) 2011-10-26 2016-04-20 吉坤日矿日石能源株式会社 Refrigerating machine working fluid composition and applications thereof
FR2986007B1 (en) * 2012-01-25 2015-01-23 Arkema France HEAT TRANSFER COMPOSITIONS HAVING IMPROVED MISCIBILITY WITH LUBRICATING OIL
FR2986236B1 (en) * 2012-01-26 2014-01-10 Arkema France HEAT TRANSFER COMPOSITIONS HAVING IMPROVED MISCIBILITY WITH LUBRICATING OIL
KR101874780B1 (en) 2012-03-27 2018-08-02 제이엑스티지 에네루기 가부시키가이샤 Working fluid composition for refrigerator
CN108707498A (en) * 2012-03-29 2018-10-26 Jxtg能源株式会社 Working fluid composition for refrigerating machine
TW201410856A (en) 2012-08-23 2014-03-16 Du Pont Refrigerant mixtures comprising tetrafluoropropenes and difluoromethane and uses thereof
FR3008419B1 (en) 2013-07-11 2015-07-17 Arkema France 2,3,3,3-TETRAFLUOROPROPENE-BASED COMPOSITIONS HAVING IMPROVED MISCIBILITY
JP6224965B2 (en) 2013-09-12 2017-11-01 出光興産株式会社 Mixing composition for refrigerator
WO2015042300A1 (en) 2013-09-19 2015-03-26 Dow Global Technologies Llc Vacuum assisted process to make closed cell rigid polyurethane foams using mixed blowing agents
WO2015050137A1 (en) 2013-10-02 2015-04-09 Jx日鉱日石エネルギー株式会社 Refrigerator oil, and working fluid composition for refrigerators
CN105916958A (en) 2014-01-16 2016-08-31 瑞孚化工产品有限公司 Desicating synthetic refrigeration lubricant composition
GB201410174D0 (en) 2014-06-09 2014-07-23 Mexichem Amanco Holding Sa Process
US10330364B2 (en) 2014-06-26 2019-06-25 Hudson Technologies, Inc. System and method for retrofitting a refrigeration system from HCFC to HFC refrigerant
JP5681829B1 (en) * 2014-07-25 2015-03-11 Jx日鉱日石エネルギー株式会社 Refrigerator oil, working fluid composition for refrigerator
JP6685277B2 (en) * 2015-03-02 2020-04-22 Jxtgエネルギー株式会社 Refrigerating machine oil and working fluid composition for refrigerator
CN105089001B (en) * 2015-04-14 2017-02-22 宁波职业技术学院 Treatment method of PM2.5 in suburban areas of Beijing
US10717694B2 (en) * 2016-05-09 2020-07-21 3M Innovative Properties Company Hydrofluoroolefins and methods of using same
JP6381614B2 (en) * 2016-11-29 2018-08-29 マクセルホールディングス株式会社 Support material composition
EP3743481B1 (en) * 2018-01-23 2022-10-05 The Chemours Company FC, LLC System and methods for introducing pag lubricant and refrigerant into an air-conditioning
US10883063B2 (en) * 2018-01-23 2021-01-05 The Chemours Company Fc, Llc Compositions, system and methods for introducing PAG lubricant or refrigerant into an air-conditioning or system using lower or low GWP refrigerant or refrigerant blends
FR3077822B1 (en) 2018-02-15 2020-07-24 Arkema France REPLACEMENT HEAT TRANSFER COMPOSITIONS FOR R-134A
WO2019173172A1 (en) 2018-03-06 2019-09-12 Shrieve Chemical Products, Inc. Lubricant and refrigerant compositions comprising polyalkylene glycols and uses thereof
US11209196B2 (en) 2018-10-26 2021-12-28 The Chemours Company Fc, Llc HFO-1234ZE, HFO-1225ZC and HFO-1234YF compositions and processes for producing and using the compositions
WO2020128504A2 (en) 2018-12-21 2020-06-25 Mexichem Fluor S.A. De C.V. Compounds
FR3139342A1 (en) * 2022-09-02 2024-03-08 Pascal RETOU Heat transfer fluid for on-board refrigeration systems.

Family Cites Families (150)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE536296A (en) 1954-03-22
BE538608A (en) 1954-06-10
US2970988A (en) 1955-10-14 1961-02-07 Minnesota Mining & Mfg New fluorine-containing polymers and preparation thereof
US2846458A (en) 1956-05-23 1958-08-05 Dow Corning Organosiloxane ethers
US2889379A (en) * 1957-02-06 1959-06-02 Dow Chemical Co Preparation of 3, 3, 3-trifluoropropene
US2931840A (en) 1958-11-25 1960-04-05 Du Pont Process for preparing 2, 3, 3, 3-tetrafluoropropene
NL251879A (en) 1959-05-22 1900-01-01
US2996555A (en) 1959-06-25 1961-08-15 Dow Chemical Co Preparation of 2, 3, 3, 3-tetrafluoropropene
DE1122697B (en) 1960-05-06 1962-01-25 Bayer Ag Process for the production of foams based on isocyanate
US3085065A (en) 1960-07-11 1963-04-09 Du Pont Process of transferring heat
FR1422125A (en) 1964-09-23 1965-12-24 Labo Cent Telecommunicat Improvements to phase-shifting circuits
US3472826A (en) 1968-05-23 1969-10-14 Union Carbide Corp Saturated hydrocarbon prepolymer and reaction products thereof
US3659023A (en) 1970-05-11 1972-04-25 Baxter Laboratories Inc Method of inducing anesthesia with 2-bromo-1 1 2 3 3-pentafluoropropane
US3884828A (en) * 1970-10-15 1975-05-20 Dow Corning Propellants and refrigerants based on trifluoropropene
US3726318A (en) * 1971-10-28 1973-04-10 Pryde Inc Faucet
US3723318A (en) * 1971-11-26 1973-03-27 Dow Corning Propellants and refrigerants based on trifluoropropene
US4465786A (en) * 1982-09-27 1984-08-14 General Electric Company Catalyst composition for the preparation of 3,3,3-trifluoropropene
US4650914A (en) 1983-07-06 1987-03-17 Monsanto Company Process for producing 1,1,2,3-tetrachloropropene
US4788352A (en) * 1986-07-21 1988-11-29 Shell Oil Company Trifluoroalkenes and a method for their preparation
JPH0688920B2 (en) 1987-02-27 1994-11-09 ダイキン工業株式会社 Method for producing 2,3,3,3-tetrafluoropropene
JPH0749391B2 (en) 1987-06-04 1995-05-31 ダイキン工業株式会社 Fluorine-containing compound and method for producing the same
US4755316A (en) * 1987-10-23 1988-07-05 Allied-Signal Inc. Refrigeration lubricants
US4798818A (en) * 1987-11-27 1989-01-17 Dow Corning Corporation Catalyst composition and process for its preparation
JPH01207250A (en) 1988-02-12 1989-08-21 Daikin Ind Ltd Production of fluorine-containing olefin
US5008428A (en) 1989-10-26 1991-04-16 W. R. Grace & Co.-Conn. Integrated process for the production of aminoacetonitriles
US5008028A (en) * 1988-12-14 1991-04-16 The Lubrizol Corporation Liquid compositions containing carboxylic esters
US4975212A (en) * 1988-12-27 1990-12-04 Allied-Signal Inc. Fluorinated lubricating compositions
US5254280A (en) * 1988-12-27 1993-10-19 Allied-Signal Inc. Refrigeration compositions having polyoxyalkylene glycols with alkylene groups having at least 4 carbon atoms therein
CA2026568C (en) 1989-02-02 1999-12-14 Shinsuke Morikawa Process for producing a hydrogen-containing 2,2-difluoropropane
US4945119A (en) 1989-05-10 1990-07-31 The Dow Chemical Company Foaming system for rigid urethane and isocyanurate foams
US4944890A (en) 1989-05-23 1990-07-31 E. I. Du Pont De Nemours And Company Compositions and process of using in refrigeration
US4971712A (en) * 1989-06-02 1990-11-20 E. I. Du Pont De Nemours And Company Compositions for compression refrigeration and methods of using them
US4971212A (en) * 1989-10-06 1990-11-20 Owens-Illinois Closure Inc. Tamper indicating packages
US4994890A (en) * 1989-11-27 1991-02-19 Snap-On Tools Corporation Rectifier structure with individual links
US5053155A (en) * 1989-12-19 1991-10-01 E. I. Du Pont De Nemours And Company Compositions and process for use in refrigeration
US5094768A (en) * 1990-03-30 1992-03-10 Lubrizol Genetics, Inc. Liquid compositions for refrigeration systems containing boron compositions
EP0602022B1 (en) 1990-07-26 1997-05-21 E.I. Du Pont De Nemours And Company Near-azeotropic blends for use as refrigerants
JPH04110388A (en) * 1990-08-31 1992-04-10 Daikin Ind Ltd Fluid for heat transfer
US5100569A (en) * 1990-11-30 1992-03-31 Allied-Signal Inc. Polyoxyalkylene glycol refrigeration lubricants having pendant, non-terminal perfluoroalkyl groups
JPH04288452A (en) 1991-03-15 1992-10-13 Daikin Ind Ltd Method of operating freezer
CA2105565C (en) 1991-03-18 2003-11-04 Robert Gerard Richard Non-azeotropic refrigerant compositions comprising difluoromethane; 1,1,1-trifluoroethane; or propane
US5182040A (en) 1991-03-28 1993-01-26 E. I. Du Pont De Nemours And Company Azeotropic and azeotrope-like compositions of 1,1,2,2-tetrafluoroethane
US5648017A (en) 1991-03-28 1997-07-15 E. I. Du Pont De Nemours And Company Azeotropic and azeotrope-like compositions of 1,1,2,2-tetrafluoroethane and (iso) butane
US5155082A (en) 1991-04-12 1992-10-13 Allied-Signal Inc. Catalyst for the manufacture of chlorofluorocarbons, hydrochlorofluorocarbons and hydrofluorocarbons
BE1005096A3 (en) 1991-07-10 1993-04-20 Solvay PROCESS FOR THE PREPARATION OF 1-chloro-1,1,3,3,3-PENTAFLUOROPROPANE AND 1,1,1,3,3,3-hexafluoropropane.
JPH0585970A (en) 1991-09-25 1993-04-06 Daikin Ind Ltd Refrigerant
US7105152B1 (en) 1991-12-18 2006-09-12 3M Innovative Properties Company Suspension aerosol formulations
US5250208A (en) 1992-04-02 1993-10-05 E. I. Du Pont De Nemours And Company Ternary azeotropic compositions
WO1993024588A1 (en) * 1992-06-03 1993-12-09 Henkel Corporation Polyol ester lubricants for high efficiency refrigerators
US5518643A (en) 1992-06-04 1996-05-21 Idemitsu Kosan Co., Ltd. Lubricating oil containing a polyvinyl ether compound for compression-type refrigerators
WO1993025510A1 (en) 1992-06-05 1993-12-23 Daikin Industries, Ltd. Processes for producing 1,1,1,2,3-pentafluoropropene and producing 1,1,1,2,3-pentafluoropropane
EP0582451B1 (en) * 1992-08-05 1997-12-10 Nippon Oil Co., Ltd. Refrigerator oil composition for fluoroalkane refrigerant
DE4233531A1 (en) * 1992-10-06 1994-04-07 Hoechst Ag Perfluorisohexene as a cooling and insulating medium
DE4241969A1 (en) * 1992-12-12 1994-06-16 Hoechst Ag High purity perfluoro (4-methyl-2-pentene), its preparation and use
GB2276392B (en) 1993-02-22 1997-03-26 D G P Improved production of natural flavours and fragrances
US5611210A (en) 1993-03-05 1997-03-18 Ikon Corporation Fluoroiodocarbon blends as CFC and halon replacements
US5538659A (en) 1993-03-29 1996-07-23 E. I. Du Pont De Nemours And Company Refrigerant compositions including hexafluoropropane and a hydrofluorocarbon
US5370812A (en) * 1993-06-28 1994-12-06 Union Carbide Chemicals & Plastics Technology Corporation Lubricant compositions for refrigerators comprising polyalkylene glycol and a hydrocarbon solvent
US5395997A (en) 1993-07-29 1995-03-07 Alliedsignal Inc. Process for the preparation of hydrofluorocarbons having 3 to 7 carbon atoms
DE69414403T2 (en) 1993-07-29 1999-05-06 Allied Signal Inc METHOD FOR PRODUCING 1,1,1,3,3 PENTAFLUORPROPANE
US6809226B1 (en) 1993-08-04 2004-10-26 Solvay (Societe Anonyme) Process for the preparation of 1-chloro-1-fluoroethane and/or 1,1-difluoroethane
US5736062A (en) 1993-08-13 1998-04-07 Ausimont S.P.A. Azeotrope-like mixtures utilizable as refrigerating fluids
US5510173A (en) 1993-08-20 1996-04-23 Southwall Technologies Inc. Multiple layer thin films with improved corrosion resistance
US5578137A (en) 1993-08-31 1996-11-26 E. I. Du Pont De Nemours And Company Azeotropic or azeotrope-like compositions including 1,1,1,2,3,4,4,5,5,5-decafluoropentane
DE69507533T2 (en) 1994-05-10 1999-06-02 Calsonic Corp Air conditioning with heat pump
US5446217A (en) * 1994-05-16 1995-08-29 Alliedsignal Inc. Processes for the preparation of fluorinated olefins and hydrofluorocarbons using fluorinated olefin
ES2104521T3 (en) 1994-07-11 1999-05-01 Allied Signal Inc PROCESS FOR THE MANUFACTURE OF 1,1,1,3,3-PENTAFLUOROPROPANE.
DE69506550D1 (en) 1994-07-14 1999-01-21 Du Pont COOLING COMPOSITIONS
US5866030A (en) * 1994-09-07 1999-02-02 Witco Corporation Enhanced hydrocarbon lubricants for use with immiscible refrigerants
US5792383A (en) * 1994-09-07 1998-08-11 Witco Corporation Reduction of enterfacial tension between hydrocarbon lubricant and immiscible liquid refrigerant
US5673144A (en) * 1994-09-14 1997-09-30 International Business Machines, Corporation Oblique viewing microscope system
JPH08157847A (en) * 1994-12-08 1996-06-18 Japan Energy Corp Lubricating oil composition for hfc fluorocarbon compressor, improvement of lubricating property of hfc fluorocarbon compressor and actuation fluid composition containing the same lubricating oil composition
RU2073058C1 (en) 1994-12-26 1997-02-10 Олег Николаевич Подчерняев Ozone-noninjurious working fluid
US5714083A (en) * 1995-01-30 1998-02-03 Turner; Donald E. A non-flammable refrigerant fluid containing hexa fluoropropane and hydrocarbons
AU704899B2 (en) 1995-07-10 1999-05-06 Idemitsu Kosan Co. Ltd A refrigerator oil and process for lubrication using the refrigerator oil
JPH09100483A (en) * 1995-10-02 1997-04-15 Japan Energy Corp Refrigerator oil and working fluid for refrigerator using the oil
IT1277085B1 (en) 1995-12-14 1997-11-04 Ausimont Spa ALMOST AZEOTROPIC TERNARY COMPOSITIONS CONSISTING OF HYDROGENATED FLUOROCARBONS AND HYDROCARBONS SUITABLE AS REFRIGERANT FLUIDS
US6235951B1 (en) 1996-01-17 2001-05-22 Central Glass Company, Limited Method for producing 1,1,1,3,3-pentafluoropropane
US6316681B1 (en) 1996-03-05 2001-11-13 Central Glass Company, Limited Method for producing 1,1,1,3,3-pentafluoropropane
US6111150A (en) 1996-06-20 2000-08-29 Central Glass Company, Limited Method for producing 1,1,1,3,3,-pentafluoropropane
JP3465865B2 (en) 1996-06-20 2003-11-10 セントラル硝子株式会社 Method for producing 1,3,3,3-tetrafluoropropene
AU4085997A (en) * 1996-08-08 1998-02-25 Donald E. Turner Alternative refrigerant including hexafluoropropylene
US5710352A (en) 1996-09-19 1998-01-20 Alliedsignal Inc. Vapor phase process for making 1,1,1,3,3-pentafluoropropane and 1-chloro-3,3,3-trifluoropropene
US6300378B1 (en) 1996-09-27 2001-10-09 University Of New Mexico Tropodegradable bromine-containing halocarbon additives to decrease flammability of refrigerants foam blowing agents solvents aerosol propellants and sterilants
US6023004A (en) 1996-11-12 2000-02-08 Alliedsignal, Inc. Liquid phase catalytic fluorination of hydrochlorocarbon and hydrochlorofluorocarbon
JP4031052B2 (en) 1997-01-31 2008-01-09 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Contact production of pentafluoropropene
US5986151A (en) 1997-02-05 1999-11-16 Alliedsignal Inc. Fluorinated propenes from pentafluoropropane
US5788886A (en) 1997-05-05 1998-08-04 E. I. Du Pont De Nemours And Company Pentafluoropropane compositions
US5988517A (en) 1997-06-09 1999-11-23 Ford Global Technologies, Inc. Method and system for controlling an automotive HVAC system based on the principle of HVAC work
FR2764883B1 (en) 1997-06-18 1999-07-16 Atochem Elf Sa PROCESS FOR THE MANUFACTURE OF HYDROFLUOROALCANES
US5969198A (en) 1997-06-27 1999-10-19 Alliedsignal Inc. Process for the preparation of 1,1,1,3,3-pentafluoropropane
US6031141A (en) 1997-08-25 2000-02-29 E. I. Du Pont De Nemours And Company Fluoroolefin manufacturing process
US6089032A (en) 1998-10-28 2000-07-18 Interdynamics Inc. Method of retrofitting air conditioner and system therefor
JP3886229B2 (en) 1997-11-11 2007-02-28 セントラル硝子株式会社 Method for producing 1,3,3,3-tetrafluoropropene
US5811603A (en) 1997-12-01 1998-09-22 Elf Atochem North America, Inc. Gas phase fluorination of 1230za
US6092589A (en) 1997-12-16 2000-07-25 York International Corporation Counterflow evaporator for refrigerants
US5856595A (en) 1998-03-03 1999-01-05 Alliedsignal Inc. Purified 1,1,1,3,3,3-hexafluoropropane and method for making same
DE19830628C1 (en) 1998-07-09 2000-04-20 Lauffer Maschf Method for crimping multilayer printed circuit boards (multilayer)
US6124510A (en) 1998-07-21 2000-09-26 Elf Atochem North America, Inc. 1234ze preparation
US6045444A (en) 1998-08-28 2000-04-04 General Motors Corporation Compact automotive air conditioning module
US6059027A (en) 1998-11-12 2000-05-09 Daimlerchrysler Corporation Anti-fog controller for reversible air conditioning and heat pump HVAC system for electric vehicles
JP2000169404A (en) 1998-12-11 2000-06-20 Tosoh Corp Bromination of fluorine-containing olefins
US6327866B1 (en) 1998-12-30 2001-12-11 Praxair Technology, Inc. Food freezing method using a multicomponent refrigerant
US6176102B1 (en) 1998-12-30 2001-01-23 Praxair Technology, Inc. Method for providing refrigeration
US6076372A (en) * 1998-12-30 2000-06-20 Praxair Technology, Inc. Variable load refrigeration system particularly for cryogenic temperatures
US6041621A (en) 1998-12-30 2000-03-28 Praxair Technology, Inc. Single circuit cryogenic liquefaction of industrial gas
US5969188A (en) * 1999-01-05 1999-10-19 Nipa Hardwicke, Inc. Process for producing trifluoromethylacetophenones
US6374629B1 (en) 1999-01-25 2002-04-23 The Lubrizol Corporation Lubricant refrigerant composition for hydrofluorocarbon (HFC) refrigerants
US6783691B1 (en) 1999-03-22 2004-08-31 E.I. Du Pont De Nemours And Company Compositions of difluoromethane, pentafluoroethane, 1,1,1,2-tetrafluoroethane and hydrocarbons
US6304803B1 (en) 1999-09-22 2001-10-16 Honda Giken Kogyo Kabushiki Kaisha HVAC control system for an automobile
EP1092573B2 (en) 1999-10-15 2007-10-31 Calsonic Kansei Corporation Heating, ventilation, and air conditioning unit for automotive vehicles
US6589355B1 (en) 1999-10-29 2003-07-08 Alliedsignal Inc. Cleaning processes using hydrofluorocarbon and/or hydrochlorofluorocarbon compounds
GB0001981D0 (en) 2000-01-31 2000-03-22 Ici Materials Refrigerant lubricant compositions
JP2004513189A (en) 2000-07-17 2004-04-30 ハネウェル・インターナショナル・インコーポレーテッド Supported catalyst system
KR20020019682A (en) 2000-09-06 2002-03-13 권오석 The composition of refrigerant mixtures for high back pressure condition
US6516837B2 (en) * 2000-09-27 2003-02-11 Honeywell International Inc. Method of introducing refrigerants into refrigeration systems
US6991744B2 (en) 2000-12-08 2006-01-31 E. I. Du Pont De Nemours And Company Refrigerant compositions containing a compatibilizer
US6548719B1 (en) 2001-09-25 2003-04-15 Honeywell International Process for producing fluoroolefins
ES2357225T3 (en) 2001-11-01 2011-04-20 Uab Research Foundation COMBINATIONS OF ANTI-DR5 ANTIBODIES AND ANTI-DR4 ANTIBODIES AND OTHER THERAPEUTIC AGENTS.
DE10203779A1 (en) 2002-01-30 2003-07-31 Solvay Fluor & Derivate Mixtures with 1,1,1,3,3-pental fluorobutane and 1,1,1,2,3,3,3-heptafluoropropane
EP2277942A3 (en) 2002-10-25 2014-07-09 Honeywell International, Incorporated. Compositions containing fluorine substituted olefins
US20040089839A1 (en) 2002-10-25 2004-05-13 Honeywell International, Inc. Fluorinated alkene refrigerant compositions
US7833433B2 (en) * 2002-10-25 2010-11-16 Honeywell International Inc. Heat transfer methods using heat transfer compositions containing trifluoromonochloropropene
US9994750B2 (en) * 2002-10-25 2018-06-12 Honeywell International Inc. Compositions containing fluorine substituted olefins and methods and systems using same
US7279451B2 (en) 2002-10-25 2007-10-09 Honeywell International Inc. Compositions containing fluorine substituted olefins
US7230146B2 (en) 2003-10-27 2007-06-12 Honeywell International Inc. Process for producing fluoropropenes
JP4110388B2 (en) * 2003-01-10 2008-07-02 荒川化学工業株式会社 Cleaning agent and rinsing agent for gold-plated parts, cleaning method and rinsing method
US7592494B2 (en) 2003-07-25 2009-09-22 Honeywell International Inc. Process for the manufacture of 1,3,3,3-tetrafluoropropene
US7524805B2 (en) * 2004-04-29 2009-04-28 Honeywell International Inc. Azeotrope-like compositions of tetrafluoropropene and hydrofluorocarbons
US6991532B2 (en) 2003-12-09 2006-01-31 Valeo Climate Control Corp. Method and apparatus for decontamination for automotive HVAC systems
FR2865731B1 (en) 2004-01-30 2007-09-07 Solvay PROCESS FOR PRODUCING A HYDROFLUOROALCAN
US7098176B2 (en) * 2004-04-16 2006-08-29 Honeywell International Inc. Azeotrope-like compositions of tetrafluoropropene and pentafluoropropene
US7341984B2 (en) * 2004-04-16 2008-03-11 Honeywell International Inc. Azeotrope-like compositions of tetrafluoropropene and trifluoroiodomethane
US6969701B2 (en) * 2004-04-16 2005-11-29 Honeywell International Inc. Azeotrope-like compositions of tetrafluoropropene and trifluoroiodomethane
US7622435B2 (en) * 2004-04-16 2009-11-24 Honeywell International Inc. Methods of replacing refrigerant
ES2392333T3 (en) 2004-04-16 2012-12-07 Honeywell International Inc. Azeotrope-like tetrafluoropropene and trifluoroiodomethane compositions
US7605117B2 (en) * 2004-04-16 2009-10-20 Honeywell International Inc. Methods of replacing refrigerant
US7074751B2 (en) * 2004-04-16 2006-07-11 Honeywell International Inc. Azeotrope-like compositions of tetrafluoropropene and trifluoroiodomethane
KR101150177B1 (en) 2004-04-16 2012-05-29 허니웰 인터내셔널 인코포레이티드 Azeotrope-like composition of tetrafluoropropene and trifluoroiodomethane
US8008244B2 (en) * 2004-04-29 2011-08-30 Honeywell International Inc. Compositions of tetrafluoropropene and hydrocarbons
CN1972887B (en) 2004-04-29 2010-10-13 霍尼韦尔国际公司 Processes for synthesis of 1,3,3,3-tetrafluoropropene
US6958424B1 (en) 2004-12-10 2005-10-25 Honeywell International Inc. Process for fluoroalkenes
US20060243944A1 (en) 2005-03-04 2006-11-02 Minor Barbara H Compositions comprising a fluoroolefin
TWI558685B (en) 2005-06-24 2016-11-21 哈尼威爾國際公司 Compositions containing fluorine substituted olefins
US20070098646A1 (en) 2005-11-01 2007-05-03 Nappa Mario J Aerosol propellants comprising unsaturated fluorocarbons
US7708903B2 (en) 2005-11-01 2010-05-04 E.I. Du Pont De Nemours And Company Compositions comprising fluoroolefins and uses thereof
US20070100010A1 (en) 2005-11-01 2007-05-03 Creazzo Joseph A Blowing agents for forming foam comprising unsaturated fluorocarbons
US7759532B2 (en) 2006-01-13 2010-07-20 E.I. Du Pont De Nemours And Company Refrigerant additive compositions containing perfluoropolyethers
US7563384B2 (en) * 2006-07-28 2009-07-21 Honeywell International Inc. Essentially non-flammable low global warming compositions
JP5285765B2 (en) * 2008-04-01 2013-09-11 ハネウェル・インターナショナル・インコーポレーテッド How to select a lubricant for a heat pump

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9919939B2 (en) 2011-12-06 2018-03-20 Delta Faucet Company Ozone distribution in a faucet
US10947138B2 (en) 2011-12-06 2021-03-16 Delta Faucet Company Ozone distribution in a faucet
US11458214B2 (en) 2015-12-21 2022-10-04 Delta Faucet Company Fluid delivery system including a disinfectant device

Also Published As

Publication number Publication date
SI2275509T1 (en) 2019-11-29
JP2017197753A (en) 2017-11-02
JP2019048996A (en) 2019-03-28
EP2277970A2 (en) 2011-01-26
CN103923611B (en) 2017-11-17
TR201708747T4 (en) 2018-11-21
EP2275509A2 (en) 2011-01-19
PT1725628E (en) 2012-07-12
PL2275509T3 (en) 2020-01-31
CN103923611A (en) 2014-07-16
JP2014159604A (en) 2014-09-04
EP2277976B1 (en) 2020-02-19
EP2277976A2 (en) 2011-01-26
KR101335360B1 (en) 2013-12-03
US20180094179A1 (en) 2018-04-05
US9631129B2 (en) 2017-04-25
PT2277970T (en) 2017-06-26
EP2009075B1 (en) 2015-05-27
EP1725628B1 (en) 2012-05-30
ES2385650T3 (en) 2012-07-27
KR20060103324A (en) 2006-09-28
EP2275509A3 (en) 2013-04-17
PL2277976T3 (en) 2020-07-27
ES2784188T3 (en) 2020-09-23
CN1898353A (en) 2007-01-17
EP2277970A3 (en) 2013-05-22
WO2005042663A1 (en) 2005-05-12
SI1725628T1 (en) 2012-09-28
US20200208034A1 (en) 2020-07-02
PT2277976T (en) 2020-04-09
US20070069175A1 (en) 2007-03-29
CN1898353B (en) 2014-05-07
EP2009075A3 (en) 2009-03-11
CN103923723A (en) 2014-07-16
ES2628746T3 (en) 2017-08-03
HUE046570T2 (en) 2020-03-30
CN103215013A (en) 2013-07-24
CN103923723B (en) 2016-09-14
DK2275509T3 (en) 2019-10-21
EP2275509B1 (en) 2019-07-17
EP2277976A3 (en) 2014-08-27
PL2277970T3 (en) 2017-09-29
JP2013166962A (en) 2013-08-29
HUE032542T2 (en) 2017-09-28
KR20120051102A (en) 2012-05-21
ES2748910T3 (en) 2020-03-18
DE08011766T1 (en) 2009-06-04
PL2009075T3 (en) 2015-10-30
JP2007510039A (en) 2007-04-19
EP2277970B1 (en) 2017-03-15
US20040089839A1 (en) 2004-05-13
CN103923610A (en) 2014-07-16
CN103923610B (en) 2018-04-10
CN103642461A (en) 2014-03-19
PT2275509T (en) 2019-10-24
DK1725628T3 (en) 2012-07-23
SI2277976T1 (en) 2020-06-30
EP2009075A2 (en) 2008-12-31
EP1725628A1 (en) 2006-11-29
JP2016104886A (en) 2016-06-09
KR101335358B1 (en) 2013-12-03
DK2277976T3 (en) 2020-04-14
CN103642461B (en) 2017-01-18
PL1725628T3 (en) 2012-09-28
ES2546024T3 (en) 2015-09-17
EP3680308A1 (en) 2020-07-15

Similar Documents

Publication Publication Date Title
US9631129B2 (en) Fluorinated alkene refrigerant compositions
EP2314654B1 (en) Compositions containing fluorine substituted olefins
EP2277977B1 (en) Compositions containing fluorine substituted olefins
JP2007510039A5 (en)
US20080111100A1 (en) Use of low gwp refrigerants comprising cf3i with stable lubricants
AU2011202712B9 (en) Compositions containing flourine substituted olefins

Legal Events

Date Code Title Description
AS Assignment

Owner name: HONEYWELL INTERNATIONAL INC., NEW JERSEY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:THOMAS, RAYMOND H.;SINGH, RAJIV R.;SIGNING DATES FROM 20170105 TO 20170107;REEL/FRAME:041679/0579

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: ADVISORY ACTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION