CA3054717A1 - Compositions containing fluorine substituted olefins - Google Patents
Compositions containing fluorine substituted olefins Download PDFInfo
- Publication number
- CA3054717A1 CA3054717A1 CA3054717A CA3054717A CA3054717A1 CA 3054717 A1 CA3054717 A1 CA 3054717A1 CA 3054717 A CA3054717 A CA 3054717A CA 3054717 A CA3054717 A CA 3054717A CA 3054717 A1 CA3054717 A1 CA 3054717A1
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- Prior art keywords
- present
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- Prior art date
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- Granted
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- 239000000203 mixture Substances 0.000 title claims abstract description 151
- 150000001336 alkenes Chemical class 0.000 title description 5
- 229910052731 fluorine Inorganic materials 0.000 title description 4
- 239000011737 fluorine Substances 0.000 title description 2
- 125000001153 fluoro group Chemical group F* 0.000 title 1
- 239000002904 solvent Substances 0.000 claims abstract description 29
- 239000000463 material Substances 0.000 claims abstract description 23
- 239000003380 propellant Substances 0.000 claims abstract description 9
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 53
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims description 6
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 claims description 6
- 239000000443 aerosol Substances 0.000 claims description 5
- 239000002537 cosmetic Substances 0.000 claims description 3
- 206010006326 Breath odour Diseases 0.000 claims description 2
- 208000032139 Halitosis Diseases 0.000 claims description 2
- 230000001088 anti-asthma Effects 0.000 claims description 2
- 239000000924 antiasthmatic agent Substances 0.000 claims description 2
- 239000002781 deodorant agent Substances 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- 239000008266 hair spray Substances 0.000 claims description 2
- 229940060367 inert ingredients Drugs 0.000 claims description 2
- 238000002483 medication Methods 0.000 claims description 2
- 239000002304 perfume Substances 0.000 claims description 2
- 238000005498 polishing Methods 0.000 claims description 2
- CDOOAUSHHFGWSA-OWOJBTEDSA-N (e)-1,3,3,3-tetrafluoroprop-1-ene Chemical compound F\C=C\C(F)(F)F CDOOAUSHHFGWSA-OWOJBTEDSA-N 0.000 claims 8
- YFMFNYKEUDLDTL-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)C(F)(F)F YFMFNYKEUDLDTL-UHFFFAOYSA-N 0.000 claims 4
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 claims 4
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 claims 4
- 239000003507 refrigerant Substances 0.000 abstract description 50
- 238000005057 refrigeration Methods 0.000 abstract description 26
- 239000004604 Blowing Agent Substances 0.000 abstract description 17
- 238000001816 cooling Methods 0.000 abstract description 7
- 238000010438 heat treatment Methods 0.000 abstract description 7
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 abstract description 2
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 description 61
- 239000012530 fluid Substances 0.000 description 28
- 239000006260 foam Substances 0.000 description 22
- 239000000314 lubricant Substances 0.000 description 17
- 239000003921 oil Substances 0.000 description 12
- 229920001515 polyalkylene glycol Polymers 0.000 description 12
- 239000007788 liquid Substances 0.000 description 11
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 10
- 238000012546 transfer Methods 0.000 description 10
- 238000007906 compression Methods 0.000 description 9
- 230000006835 compression Effects 0.000 description 9
- 238000004378 air conditioning Methods 0.000 description 8
- 238000004140 cleaning Methods 0.000 description 8
- 239000007791 liquid phase Substances 0.000 description 8
- 230000008569 process Effects 0.000 description 8
- 230000001954 sterilising effect Effects 0.000 description 8
- 229910052801 chlorine Inorganic materials 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- -1 compatibilzers Substances 0.000 description 7
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- 229920002635 polyurethane Polymers 0.000 description 6
- 239000004814 polyurethane Substances 0.000 description 6
- 238000004659 sterilization and disinfection Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- 238000005273 aeration Methods 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 229920000582 polyisocyanurate Polymers 0.000 description 5
- 239000011495 polyisocyanurate Substances 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 231100000419 toxicity Toxicity 0.000 description 5
- 230000001988 toxicity Effects 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000000356 contaminant Substances 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 239000003063 flame retardant Substances 0.000 description 4
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 4
- 230000001965 increasing effect Effects 0.000 description 4
- 239000010687 lubricating oil Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 239000012808 vapor phase Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 238000005238 degreasing Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 231100000053 low toxicity Toxicity 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 229920002120 photoresistant polymer Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 230000001629 suppression Effects 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229920004449 Halon® Polymers 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 210000003850 cellular structure Anatomy 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000010696 ester oil Substances 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 231100000824 inhalation exposure Toxicity 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920013639 polyalphaolefin Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 239000004155 Chlorine dioxide Substances 0.000 description 1
- XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical compound FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 102100038019 Corticotropin-releasing factor receptor 2 Human genes 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 101000878664 Homo sapiens Corticotropin-releasing factor receptor 2 Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical class CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- RREGISFBPQOLTM-UHFFFAOYSA-N alumane;trihydrate Chemical class O.O.O.[AlH3] RREGISFBPQOLTM-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000000926 atmospheric chemistry Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- YNKZSBSRKWVMEZ-UHFFFAOYSA-N bromo-chloro-fluoromethane Chemical class FC(Cl)Br YNKZSBSRKWVMEZ-UHFFFAOYSA-N 0.000 description 1
- RJCQBQGAPKAMLL-UHFFFAOYSA-N bromotrifluoromethane Chemical compound FC(F)(F)Br RJCQBQGAPKAMLL-UHFFFAOYSA-N 0.000 description 1
- 235000013844 butane Nutrition 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 235000019398 chlorine dioxide Nutrition 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000003682 fluorination reaction Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000005828 hydrofluoroalkanes Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- BWHLPLXXIDYSNW-UHFFFAOYSA-N ketorolac tromethamine Chemical compound OCC(N)(CO)CO.OC(=O)C1CCN2C1=CC=C2C(=O)C1=CC=CC=C1 BWHLPLXXIDYSNW-UHFFFAOYSA-N 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 235000012254 magnesium hydroxide Nutrition 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical class CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical class [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005903 polyol mixture Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Chemical class 0.000 description 1
- 229920000915 polyvinyl chloride Chemical class 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- HQUQLFOMPYWACS-UHFFFAOYSA-N tris(2-chloroethyl) phosphate Chemical compound ClCCOP(=O)(OCCCl)OCCCl HQUQLFOMPYWACS-UHFFFAOYSA-N 0.000 description 1
- GTRSAMFYSUBAGN-UHFFFAOYSA-N tris(2-chloropropyl) phosphate Chemical compound CC(Cl)COP(=O)(OCC(C)Cl)OCC(C)Cl GTRSAMFYSUBAGN-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
- C09K5/041—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
- C09K5/044—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N27/00—Biocides, pest repellants or attractants, or plant growth regulators containing hydrocarbons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/18—Liquid substances or solutions comprising solids or dissolved gases
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B08—CLEANING
- B08B—CLEANING IN GENERAL; PREVENTION OF FOULING IN GENERAL
- B08B3/00—Cleaning by methods involving the use or presence of liquid or steam
- B08B3/04—Cleaning involving contact with liquid
- B08B3/08—Cleaning involving contact with liquid the liquid having chemical or dissolving effect
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/143—Halogen containing compounds
- C08J9/144—Halogen containing compounds containing carbon, halogen and hydrogen only
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/06—Organic materials
- C09K21/08—Organic materials containing halogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/007—Organic compounds containing halogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
- C09K5/041—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
- C09K5/044—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
- C09K5/045—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
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- F25B39/00—Evaporators; Condensers
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-
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- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25B—REFRIGERATION MACHINES, PLANTS OR SYSTEMS; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS
- F25B39/00—Evaporators; Condensers
- F25B39/04—Condensers
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
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Abstract
The use of pentafluoropropene (HFO-1225) and tetrafluoropropene (HFO-1234) in refrigeration equipment is disclosed. These materials are generally useful as refrigerants for heating and cooling, as blowing agents, as aerosol propellants, as solvent composition, and as fire extinguishing and suppressing agents.
Description
COMPOSITIONS CONTAINING FLUORINE SUBSTITUTED OLEFINS
=
= FIELD OF THE INVENTION
This invention relates to compositions having utility in numerous applications, including particularly refrigeration systems, and to methods and systems which =
utilize such compositions. In preferred aspects, the present invention is directed to refrigerant compositions which comprise at least one multi-fluorinated olefin of the present invention. 0=
BACKGROUND OF THE INVENTION
Fluorocarbon based fluids have found widespread use in many commerr,ial ' 25 and industrial applications. For example, fluorocarbon based fluids are frequently used as a working fluid in systems such as air conditioning, heat pump and refrigeration applications. The vapor compression cycle is one of the most = commonly used typetnethods to accomplish cooling or heating in a refrigeration system. The vapor compression cycle usually involves the phase change of the refrigerant from the liquid to the vapor phase through heat absorption at a relatively low pressure and then from the vapor to the liquid phase through heat removal at a =
relatively low pressure and temperature, compressing the vapor to a relatively =
=
elevated pressure, condensing the vapor to the liquid phase through heat removal at this relatively elevated pressure and temperature, and then reducing the pressure to start the cycle over again.
While the primary purpose of refrigeration is to remove heat from an object or other fluid at a relatively low temperature, the primary purpose of a heat pump is to =
add heat at a higher temperature relative to the environment Certain fluorocarbons have been a preferred component in many heat exchange fluids, such as refrigerants, for many years in many applications.
For, example, fluoroalkanes, such as chlorofluoromethane and chlorofluordethane derivatives, have gained widespread use as refrigerants in applications including air conditioning and heat pump applications owing to their unique combination of chemical and physical properties. Many of the refrigerants commonly utilized in vapor Compression systems are either single components fluids or azeotropic mixtures.
. 15 Concern has increased in recent years about potential damage to the earth's atmosphere and climate, and certain chlorine-based compounds have been Identified as particularly problematic in this regard. The use of chlorine-containing compositions (such as chlorofluorocarbons (CFCs), hydrochlorofluorocarbons (HCFs) and the like) as refrigerants in air-conditioning and refrigeration systems has become disfavored because of the ozone-depleting properties associated with many of such compounds. There has thus been an increasing need for new fluorocarbon and hydrofluorocarbon compounds and compositions that offer alternatives for refrigeration and heat pump applications. For example, 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 (HFCs).
It is generally considered Important, however, that any potential substitute = refrigerant must also possess those properties present in many of the most widely used fluids, such as excellent heat transfer properties, chemical stability, low- or no-30. toxicity, non-flammability and lubricant compatibility, among others.
Applicants have come to appreciate that lubricant compatibility is of particular Importance in many of applications. More particularly, it Is highly desirably for
=
= FIELD OF THE INVENTION
This invention relates to compositions having utility in numerous applications, including particularly refrigeration systems, and to methods and systems which =
utilize such compositions. In preferred aspects, the present invention is directed to refrigerant compositions which comprise at least one multi-fluorinated olefin of the present invention. 0=
BACKGROUND OF THE INVENTION
Fluorocarbon based fluids have found widespread use in many commerr,ial ' 25 and industrial applications. For example, fluorocarbon based fluids are frequently used as a working fluid in systems such as air conditioning, heat pump and refrigeration applications. The vapor compression cycle is one of the most = commonly used typetnethods to accomplish cooling or heating in a refrigeration system. The vapor compression cycle usually involves the phase change of the refrigerant from the liquid to the vapor phase through heat absorption at a relatively low pressure and then from the vapor to the liquid phase through heat removal at a =
relatively low pressure and temperature, compressing the vapor to a relatively =
=
elevated pressure, condensing the vapor to the liquid phase through heat removal at this relatively elevated pressure and temperature, and then reducing the pressure to start the cycle over again.
While the primary purpose of refrigeration is to remove heat from an object or other fluid at a relatively low temperature, the primary purpose of a heat pump is to =
add heat at a higher temperature relative to the environment Certain fluorocarbons have been a preferred component in many heat exchange fluids, such as refrigerants, for many years in many applications.
For, example, fluoroalkanes, such as chlorofluoromethane and chlorofluordethane derivatives, have gained widespread use as refrigerants in applications including air conditioning and heat pump applications owing to their unique combination of chemical and physical properties. Many of the refrigerants commonly utilized in vapor Compression systems are either single components fluids or azeotropic mixtures.
. 15 Concern has increased in recent years about potential damage to the earth's atmosphere and climate, and certain chlorine-based compounds have been Identified as particularly problematic in this regard. The use of chlorine-containing compositions (such as chlorofluorocarbons (CFCs), hydrochlorofluorocarbons (HCFs) and the like) as refrigerants in air-conditioning and refrigeration systems has become disfavored because of the ozone-depleting properties associated with many of such compounds. There has thus been an increasing need for new fluorocarbon and hydrofluorocarbon compounds and compositions that offer alternatives for refrigeration and heat pump applications. For example, 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 (HFCs).
It is generally considered Important, however, that any potential substitute = refrigerant must also possess those properties present in many of the most widely used fluids, such as excellent heat transfer properties, chemical stability, low- or no-30. toxicity, non-flammability and lubricant compatibility, among others.
Applicants have come to appreciate that lubricant compatibility is of particular Importance in many of applications. More particularly, it Is highly desirably for
2 =
refrigesation fluids to be compatible with the lubricant utilized in the compressor unit, used in most refrigeration systems. Unfortunately, many nowdfrodne-containing refrigeration fluids, including HFC's, are relatively insoluble ancVor ImMiscible in the types of lubricants used traditionally with CFC's and HFC's, including, for example.
mineral oils, allryiberizenes or poly(alpha-olefins). In order for a refrigeration told-lubricant combination to walk at a desirable level of efficiently within a compression refrigeration, air-conditioning andfor heat punip system, the lubricant should be sufficiently soluble in the refrigeration liquid over a wide range of operating temperatures. Such solubility lowers the viscosity of the lubdcant and allows it to flow more easily throughout the system. In the absence of such solubill%
lubricants tend to become lodged in the coils of the evaporator of the refrigerafron, conditioning or heat pump system, as well as other parts of the system, and thus reduce the system efficiency.
With regard to efficiency in use, Ills Important to note that a loss in refrigerant thermodynamic performance or energy efficiency may have secondary environmental knpects through Increased fossil fuel usage arising from an increased demand for electrical energy.
Furthermore. it is generally considered desirably for CFC refrigerant =
substitutes to be effective without major engineering changes to conventional vapor compression technology currently used with CFC refrigeraMs.
Flammability is another imperilled property for many applications. 'That is.
It is considered either important or essential in many applications, including particularly in hest transfer applications, to use compositions which are nco-remmable. Thus, it is frequently benencial 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 as determined in accordance with ASTM standard E-681. dated Unfortunately, many HFC's which might otherwise be desirable for used In refrigerant compositions are not nonflammable. For maniple, the fluoroalkane dinuoreethane (HFC-152a) and the fluctuation* 1.1.1¨frilluorpropene (HF0-12434 are each flammable and therefore not viable for use in many aPerceiktne-1-figher fluorosikenes, that is fluorine-subsetuted arenas having at least five
refrigesation fluids to be compatible with the lubricant utilized in the compressor unit, used in most refrigeration systems. Unfortunately, many nowdfrodne-containing refrigeration fluids, including HFC's, are relatively insoluble ancVor ImMiscible in the types of lubricants used traditionally with CFC's and HFC's, including, for example.
mineral oils, allryiberizenes or poly(alpha-olefins). In order for a refrigeration told-lubricant combination to walk at a desirable level of efficiently within a compression refrigeration, air-conditioning andfor heat punip system, the lubricant should be sufficiently soluble in the refrigeration liquid over a wide range of operating temperatures. Such solubility lowers the viscosity of the lubdcant and allows it to flow more easily throughout the system. In the absence of such solubill%
lubricants tend to become lodged in the coils of the evaporator of the refrigerafron, conditioning or heat pump system, as well as other parts of the system, and thus reduce the system efficiency.
With regard to efficiency in use, Ills Important to note that a loss in refrigerant thermodynamic performance or energy efficiency may have secondary environmental knpects through Increased fossil fuel usage arising from an increased demand for electrical energy.
Furthermore. it is generally considered desirably for CFC refrigerant =
substitutes to be effective without major engineering changes to conventional vapor compression technology currently used with CFC refrigeraMs.
Flammability is another imperilled property for many applications. 'That is.
It is considered either important or essential in many applications, including particularly in hest transfer applications, to use compositions which are nco-remmable. Thus, it is frequently benencial 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 as determined in accordance with ASTM standard E-681. dated Unfortunately, many HFC's which might otherwise be desirable for used In refrigerant compositions are not nonflammable. For maniple, the fluoroalkane dinuoreethane (HFC-152a) and the fluctuation* 1.1.1¨frilluorpropene (HF0-12434 are each flammable and therefore not viable for use in many aPerceiktne-1-figher fluorosikenes, that is fluorine-subsetuted arenas having at least five
3 carbon atoms, have been suggested for use as refrigerants. U.S. Patent No.
4,788,352 ¨ Smutny is directed to production of fluorinated Cs to Cs 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.
(See column 1, lines 11 ¨ 22).
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.
Bromofiuoromethane and bromochlorofluoromethane derivatives, particularly bromotrifiuoromethane (Halon 1301) and bromochlorodffluoromethane (Heron 1211) have gained widespread use as fire extinguishing agents in enclosed areas such as airplane cabins and computer moms. However, the use of various halons is being phased out due to their high ozone depletion. Moreover, as halons are frequently used in areas where humans are present, suitable replacements must also be safe to humans at concentrations necessary to suppress or extinguish fire.
= Applicants have thus come to appreciate a need for compositions, and particularly heat transfer compositions, fire extinguishing/suppression compositions.
blowing agents, solvent compositions, and cornpatabilizing agents, 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.
=
SUMMARY
Applicants have found that the above-noted need, and other needs, can be satisfied by compositions comprising one or more C3 or C4 fluoroalkenes, preferably compounds having Formula I as follows:
XCF:113. 0) where X is a C2 or a C3 unsaturated, substituted or unsubstituted, alkyl radical, each R Is independently Cl, F, Br, I or H, and z Is 1 to 3.
The present invention provides also methods and systems which utilize the compositions of the present invention, including methods and systems for heat transfer, foam blowing, solvating, and aerosol generation.
=
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 fluoroalitene compounds of the present invention are sometimes referred to herein for the purpose of convenience as hydrofluoro-olefins or "HFOs" if they contain at least one hydrogen Although it is contemplated that the HFOs of the president mentioned 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:
=
R>=11--"
(II) where each R is independently Cl, F, Br, I or H
11` is (CR2)Y,
(See column 1, lines 11 ¨ 22).
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.
Bromofiuoromethane and bromochlorofluoromethane derivatives, particularly bromotrifiuoromethane (Halon 1301) and bromochlorodffluoromethane (Heron 1211) have gained widespread use as fire extinguishing agents in enclosed areas such as airplane cabins and computer moms. However, the use of various halons is being phased out due to their high ozone depletion. Moreover, as halons are frequently used in areas where humans are present, suitable replacements must also be safe to humans at concentrations necessary to suppress or extinguish fire.
= Applicants have thus come to appreciate a need for compositions, and particularly heat transfer compositions, fire extinguishing/suppression compositions.
blowing agents, solvent compositions, and cornpatabilizing agents, 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.
=
SUMMARY
Applicants have found that the above-noted need, and other needs, can be satisfied by compositions comprising one or more C3 or C4 fluoroalkenes, preferably compounds having Formula I as follows:
XCF:113. 0) where X is a C2 or a C3 unsaturated, substituted or unsubstituted, alkyl radical, each R Is independently Cl, F, Br, I or H, and z Is 1 to 3.
The present invention provides also methods and systems which utilize the compositions of the present invention, including methods and systems for heat transfer, foam blowing, solvating, and aerosol generation.
=
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 fluoroalitene compounds of the present invention are sometimes referred to herein for the purpose of convenience as hydrofluoro-olefins or "HFOs" if they contain at least one hydrogen Although it is contemplated that the HFOs of the president mentioned 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:
=
R>=11--"
(II) where each R is independently Cl, F, Br, I or H
11` is (CR2)Y,
5 Y is CRF2 and n is 0 or 1.
In highly preferred embodiments. '(Is CFs. n is 0 and at least one of the remaining Rs is F.
Applicants believe that, in general, the compounds of the above identified Formulas I and II are generally effective and exhibit utility in refrigerant compositions, blowing agent compositions, compatibilzers, and solvent compositions of the present invention. However, applicants have surprisingly and unexpectedly found that certain ails compounds having a structure in accordance with the formulas described above exhibit ahighly 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, applicants believe that a relatively low toxicity level is associated with compounds of Formula II, preferably wherein Y is CF,. wherein at least one R
on the unsaturated terminal carbon is H. and at least one of the remaining Rs is F.
Applicants believe 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 tetrafluoropropenes (HFO-1234), pentalluoropropenes (HFO-1225) and combinations of these.
It is even more preferred that the compounds of the present invention are the tetrafluoroprpoene and pentafluoropropene compounds in which the unsaturated terminal carbon has not more than one F substituent, specifically: 1, 3, 3, 3-tetrailuoropropene (HF0-1234Ze); 2, 3, 3. 3-tetrafluoropropene (HF0-1234yf);
and 1,2.3,3,3-pentefluoropropene (HF0-1225ye). and any and all stereoisomers of each of these. Applicant has discovered that such compounds have a very low acute toxicity level, as measured by inhalation exposure to mice and rats. On the other hand, applicants have found that a relatively high degree of toxicity may be
In highly preferred embodiments. '(Is CFs. n is 0 and at least one of the remaining Rs is F.
Applicants believe that, in general, the compounds of the above identified Formulas I and II are generally effective and exhibit utility in refrigerant compositions, blowing agent compositions, compatibilzers, and solvent compositions of the present invention. However, applicants have surprisingly and unexpectedly found that certain ails compounds having a structure in accordance with the formulas described above exhibit ahighly 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, applicants believe that a relatively low toxicity level is associated with compounds of Formula II, preferably wherein Y is CF,. wherein at least one R
on the unsaturated terminal carbon is H. and at least one of the remaining Rs is F.
Applicants believe 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 tetrafluoropropenes (HFO-1234), pentalluoropropenes (HFO-1225) and combinations of these.
It is even more preferred that the compounds of the present invention are the tetrafluoroprpoene and pentafluoropropene compounds in which the unsaturated terminal carbon has not more than one F substituent, specifically: 1, 3, 3, 3-tetrailuoropropene (HF0-1234Ze); 2, 3, 3. 3-tetrafluoropropene (HF0-1234yf);
and 1,2.3,3,3-pentefluoropropene (HF0-1225ye). and any and all stereoisomers of each of these. Applicant has discovered that such compounds have a very low acute toxicity level, as measured by inhalation exposure to mice and rats. On the other hand, applicants have found that a relatively high degree of toxicity may be
6 =
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, applicants have discovered that 1,1,3,3.3-pentafluoropropene (HFO-1225ze) exhibits an unacceptably high degree of toxicity, as measured by inhalation exposure to mice and rats.
The preferred compounds of the present invention, namely, HF0-1225 and HFO-1234 are known materials and are listed in Chemical Abstracts databases.
=
HF0-1225 is commercially available, from example from Syntex Chemical Co.
Futhermore, methods are described generally in the patent literature for producing fluoroalkenes. For example, the production of fluoropmpenes such as CF3CH=CH2 by catalytic vapor phase fluorination of various saturated and unsaturated halogen-containing C3 compounds is described in U.S. Patent Nos. 2,889,379; 4,798,818 and 4.465,786. U.S. Patent No.
5,532,419. discloses a vapor phase catalytic process for the preparation of fluoroalkene using a chloro- or bromo-halofluorocarbon and HF. EP 974.571, "
discloses the preparation of 1 ,1,1 .3-tetrafluoroproperie by contacting 1 .1 pentafluoropropane (HFC-2451a) 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 Number 7,230,146 entitled -Process for Producing Fluoqxopenee .
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 fluorooiefins 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
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, applicants have discovered that 1,1,3,3.3-pentafluoropropene (HFO-1225ze) exhibits an unacceptably high degree of toxicity, as measured by inhalation exposure to mice and rats.
The preferred compounds of the present invention, namely, HF0-1225 and HFO-1234 are known materials and are listed in Chemical Abstracts databases.
=
HF0-1225 is commercially available, from example from Syntex Chemical Co.
Futhermore, methods are described generally in the patent literature for producing fluoroalkenes. For example, the production of fluoropmpenes such as CF3CH=CH2 by catalytic vapor phase fluorination of various saturated and unsaturated halogen-containing C3 compounds is described in U.S. Patent Nos. 2,889,379; 4,798,818 and 4.465,786. U.S. Patent No.
5,532,419. discloses a vapor phase catalytic process for the preparation of fluoroalkene using a chloro- or bromo-halofluorocarbon and HF. EP 974.571, "
discloses the preparation of 1 ,1,1 .3-tetrafluoroproperie by contacting 1 .1 pentafluoropropane (HFC-2451a) 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 Number 7,230,146 entitled -Process for Producing Fluoqxopenee .
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 fluorooiefins 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
7 compositions also do not contribute substantially to global warning compared to many of the hydrofluoroalkanes presently in use.
Preferably, the compositions of the present Invention have a Global Warming Potential (GWP) of not greater than 150, more preferably not greater than 100 and even more preferably not greater than 75. As used herein, "GWP- Is measured relative to that of carbon dioxide and over a 100 year time horizon, as defined in "The Scientific Assessment of Ozone Depletion, 2002, a report of the World Meteorological Association's Global Ozone Research and Monitoring Project".
The present compositions also preferably have an Ozone Depletion Potential (ODP) of not greater than 0.05, more preferably not greater than 0.02 and even more preferably about zero. As used herein, "ODP" is as defined in "The Scientific Assessment of Ozone Depletion, 2002. A report of the World Meteorological Association's Global Ozone Research and Monitoring Project".
HEAT TRANSFER COMPOSITIONS
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.
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
Preferably, the compositions of the present Invention have a Global Warming Potential (GWP) of not greater than 150, more preferably not greater than 100 and even more preferably not greater than 75. As used herein, "GWP- Is measured relative to that of carbon dioxide and over a 100 year time horizon, as defined in "The Scientific Assessment of Ozone Depletion, 2002, a report of the World Meteorological Association's Global Ozone Research and Monitoring Project".
The present compositions also preferably have an Ozone Depletion Potential (ODP) of not greater than 0.05, more preferably not greater than 0.02 and even more preferably about zero. As used herein, "ODP" is as defined in "The Scientific Assessment of Ozone Depletion, 2002. A report of the World Meteorological Association's Global Ozone Research and Monitoring Project".
HEAT TRANSFER COMPOSITIONS
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.
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
8 =
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. Patent No. 6,516,837.
Commonly used refrigeration lubricants such as Polyol Esters (POEs) and Poly AlIcylene Glycols (PAGs) that are used in refrigeration machinery with hydrofluorocarbon (HFC) refrigerants may be used with the refrigerant compositions of the present invention.
BLOWING AGENTS, FOAMS AND FOAMABLE COMPOSITIONS
Blowing agents may also comprise or constitute one or more of the present compositions. As mentioned above, the compositions of the present invention may Include the compounds of the present invention in widely ranging amounts.. It is generally preferred, however, that for preferred composhions for use as blowing agents in accordance with the present invention, compound(s) in accordance with Formula I. and even more preferably Formula IL 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.
In other .embodiments, the invention provides foamable compositions, and preferably polyurethane.polyisocyanurate and extruded thermoplastic foam compositions, prepared using the compositions of the present invention. In such foam embodiments, one or more of the present compositions are included as or part of a blowing agent In a foamable composition, which composition preferably Includes one or more additional components capable of reacting and/or foaming under the proper conditions to form a foam or cellular structure, as Is well known in the art.
The invention also relates to foam. and preferably closed cell foam, prepared from a polymer foam formulation containing a blowing agent comprising the compositions of the invention. In yet another embodiments. the invention provides a foamable composition comprising thermoplastic foams, such as polystyrene and polyethylene (PE), preferably low density PE.
in certain preferred =embodiments, dispersing agents, cell stabilizers, surfactants and other additives may also be incorporated into the blowing agent compositions of the present invention. Surfactants are optionally but preferably =
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. Patent No. 6,516,837.
Commonly used refrigeration lubricants such as Polyol Esters (POEs) and Poly AlIcylene Glycols (PAGs) that are used in refrigeration machinery with hydrofluorocarbon (HFC) refrigerants may be used with the refrigerant compositions of the present invention.
BLOWING AGENTS, FOAMS AND FOAMABLE COMPOSITIONS
Blowing agents may also comprise or constitute one or more of the present compositions. As mentioned above, the compositions of the present invention may Include the compounds of the present invention in widely ranging amounts.. It is generally preferred, however, that for preferred composhions for use as blowing agents in accordance with the present invention, compound(s) in accordance with Formula I. and even more preferably Formula IL 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.
In other .embodiments, the invention provides foamable compositions, and preferably polyurethane.polyisocyanurate and extruded thermoplastic foam compositions, prepared using the compositions of the present invention. In such foam embodiments, one or more of the present compositions are included as or part of a blowing agent In a foamable composition, which composition preferably Includes one or more additional components capable of reacting and/or foaming under the proper conditions to form a foam or cellular structure, as Is well known in the art.
The invention also relates to foam. and preferably closed cell foam, prepared from a polymer foam formulation containing a blowing agent comprising the compositions of the invention. In yet another embodiments. the invention provides a foamable composition comprising thermoplastic foams, such as polystyrene and polyethylene (PE), preferably low density PE.
in certain preferred =embodiments, dispersing agents, cell stabilizers, surfactants and other additives may also be incorporated into the blowing agent compositions of the present invention. Surfactants are optionally but preferably =
9 added to serve as cell stabilizers. Some representative materials are sold under the names of DC-193. B-8404, and 1-5340 which are, generally, polysiloxane polyoxyalkylene block co-polymers such as those disclosed In U.S. Patent Nos.
2,834,748, 2.917,480, and 2,846,458.
Other optional additives for the blowing agent mixture may include flame retardants such as tri(2-chloroethyl)phosphate, tri(2-chloropropyl)phosphate, tri(2,3-dbromopropyl)-phosphate, tri(1 .3-dichloropmpyl) phosphate, diammonkm phosphate, various halogenated aromatic compounds, antimony oxide, aluminum trihydrate, polyvinyl chloride, and the like.
PROPELLANT COMPOSMONS
In another aspect, the present Invention provided propellant compositions comprising or consisting essentially of a composition of the present Invention, such propellant composition preferably being a sprayable composition. The propellant compositions of the presenfinvention preferably comprise a material to be sprayed and a propellant comprising, consisting essentially of, or consisting of a composition In accordance with the present Invention. Inert Ingredients, solvents, and other materials may also be present in the sprayable mixture. Preferably, the sprayable composition is an aerosol. Suitable materials to be sprayed include, without limitation, cosmetic materials such as deodorants, perfumes, hair sprays, cleansers, and polishing agents as well as medicinal materials such as anti-asthma and anti-halitosis medications.
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 present compositions are also advantageous for in use in systems and methods of generating aerosols.
preferably comprising or consisting of the aerosol propellant in such systems and methods.
=
Methods of forming foams and methods of extinguishing and suppressing fire are also included in certain aspects of the present Invention. The present invention also
2,834,748, 2.917,480, and 2,846,458.
Other optional additives for the blowing agent mixture may include flame retardants such as tri(2-chloroethyl)phosphate, tri(2-chloropropyl)phosphate, tri(2,3-dbromopropyl)-phosphate, tri(1 .3-dichloropmpyl) phosphate, diammonkm phosphate, various halogenated aromatic compounds, antimony oxide, aluminum trihydrate, polyvinyl chloride, and the like.
PROPELLANT COMPOSMONS
In another aspect, the present Invention provided propellant compositions comprising or consisting essentially of a composition of the present Invention, such propellant composition preferably being a sprayable composition. The propellant compositions of the presenfinvention preferably comprise a material to be sprayed and a propellant comprising, consisting essentially of, or consisting of a composition In accordance with the present Invention. Inert Ingredients, solvents, and other materials may also be present in the sprayable mixture. Preferably, the sprayable composition is an aerosol. Suitable materials to be sprayed include, without limitation, cosmetic materials such as deodorants, perfumes, hair sprays, cleansers, and polishing agents as well as medicinal materials such as anti-asthma and anti-halitosis medications.
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 present compositions are also advantageous for in use in systems and methods of generating aerosols.
preferably comprising or consisting of the aerosol propellant in such systems and methods.
=
Methods of forming foams and methods of extinguishing and suppressing fire are also included in certain aspects of the present Invention. The present invention also
10 =
provides in certain aspects methods of removing residue from articles in which the present compositions are used as solvent compositions in such methods and systems.
HEAT TRANSFER METHODS
= 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 changing the phase of the composition. For example, the present methods provide cooling by absorbing heat from a fluid or article, preferably by evaporating the present refrigerant composition in the vicinity of the body or fluid to be cooled to produce vapor comprising the present composition. Preferably the methods include the further step of compressing the refrigerant vapor, usually with a compressor or similar equipment to produce vapor of the present composition at a relatively elevated pressure. Generally, the step of compressing the vapor results in the addition of heat to the vapor, thus causing an increase in the temperature of the relatively high pressure vapor. Preferrably, the present methods include removing from this relatively high temperature, high pressure vapor at least a portion of the heat added by the evaporation and compression steps. The heat removal step preferably includes condensing the high temperature, high pressure vapor while the vapor is in a relatively high pressure Condition to produce a relatively high pressure liquid comprising a composition of the present invention. This relatively high pressure liquid preferably then undergoes a nominally isoenthalpic reduction in pressure to produce a relatively low temperature, low pressure liquid. 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.. Such methods, as mentioned hereinbefore, frequently are reverse cycles to the refrigeration cycle described above.
= FOAM BLOWING METHODS
provides in certain aspects methods of removing residue from articles in which the present compositions are used as solvent compositions in such methods and systems.
HEAT TRANSFER METHODS
= 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 changing the phase of the composition. For example, the present methods provide cooling by absorbing heat from a fluid or article, preferably by evaporating the present refrigerant composition in the vicinity of the body or fluid to be cooled to produce vapor comprising the present composition. Preferably the methods include the further step of compressing the refrigerant vapor, usually with a compressor or similar equipment to produce vapor of the present composition at a relatively elevated pressure. Generally, the step of compressing the vapor results in the addition of heat to the vapor, thus causing an increase in the temperature of the relatively high pressure vapor. Preferrably, the present methods include removing from this relatively high temperature, high pressure vapor at least a portion of the heat added by the evaporation and compression steps. The heat removal step preferably includes condensing the high temperature, high pressure vapor while the vapor is in a relatively high pressure Condition to produce a relatively high pressure liquid comprising a composition of the present invention. This relatively high pressure liquid preferably then undergoes a nominally isoenthalpic reduction in pressure to produce a relatively low temperature, low pressure liquid. 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.. Such methods, as mentioned hereinbefore, frequently are reverse cycles to the refrigeration cycle described above.
= FOAM BLOWING METHODS
11 One embodiment of the present invention relates to methods of forming foams, and preferably polyurethane and polyisocyanurate foams. The methods generally comprise providing a blowing agent composition of the present inventions, adding (directly or indirectly) the blowing agent composition to a foamable composition, and reacting the foamable composition under the conditions effective to form a foam or cellular structure. as Is well known in the art. Any of the methods well known in the art, such as those described in "Polyurethanes Chemistry and Technology," Volumes I and IL Saunders and Frisch. 1962, John Wiley and Sons, New York, NY. may be used or adapted .. for use in accordance with the foam embodiments of the present invention.
In general, such preferred methods comprise preparing polyurethane or PolYisocyanurate foams by combining an isocyanate, a polyol or mixture of polyols. a blowing agent or mixture of blowing agents comprising one or more of the present compositions, and other materials such as catalysts, surfactants, and optionally.
flame retardants, colorants, or other additives.
It is convenient in many applications to provide the components for polyurethane or polyisocyanurate foams in pre-blended formulations. Most typically, the foam formulation is pre-blended into two components. The isocyanate and optionally certain surfactants and blowing agents comprise the first component, commonly referred to as. the "A" component. The polyol or polyol mixture, surfactant, catalysts, blowing agents, flame retardant, and other isocyanate reactive components comprise the second component, commonly referred to as the "B"
component. Accordingly, polyurethane or polyisocyanurate foams are readily prepared by bringing together the A and B side components either by hand mix for small preparations and, preferably, machine mix techniques to form blocks, slabs, laminates, pour-in-place panels and other items, spray applied foams, froths, and the like. Optionally, other ingredients such as fire retardants, colorants, acedliary blowing agents, and even other polyola can be added as a third stream to the mix head or reaction site. Most preferably, however, they are all incorporated into one B-component as described above.
It is also possible to produce thermoplastic foams using the compositions of the invention. For example, conventional polystyrene and polyethylene formulations
In general, such preferred methods comprise preparing polyurethane or PolYisocyanurate foams by combining an isocyanate, a polyol or mixture of polyols. a blowing agent or mixture of blowing agents comprising one or more of the present compositions, and other materials such as catalysts, surfactants, and optionally.
flame retardants, colorants, or other additives.
It is convenient in many applications to provide the components for polyurethane or polyisocyanurate foams in pre-blended formulations. Most typically, the foam formulation is pre-blended into two components. The isocyanate and optionally certain surfactants and blowing agents comprise the first component, commonly referred to as. the "A" component. The polyol or polyol mixture, surfactant, catalysts, blowing agents, flame retardant, and other isocyanate reactive components comprise the second component, commonly referred to as the "B"
component. Accordingly, polyurethane or polyisocyanurate foams are readily prepared by bringing together the A and B side components either by hand mix for small preparations and, preferably, machine mix techniques to form blocks, slabs, laminates, pour-in-place panels and other items, spray applied foams, froths, and the like. Optionally, other ingredients such as fire retardants, colorants, acedliary blowing agents, and even other polyola can be added as a third stream to the mix head or reaction site. Most preferably, however, they are all incorporated into one B-component as described above.
It is also possible to produce thermoplastic foams using the compositions of the invention. For example, conventional polystyrene and polyethylene formulations
12 =
may be combined with the corm:monism in a conventional manner to produce rigid foams.
CLEANING METHODS
The present invention also provides methods of removing containments from a product, part, component, substrate, or any other article or portion thereof by applying to the article a composition of the present invention. For the purposes of convenience, the term "article" is used herein to refer to all such products, parts, components, substrates, and the like and is further intended to refer to any surface or portion thereof. Furthermore, the term "contaminant" is Intended to refer to any unwanted material or substance present on the article, even if such substance is placed on the article intentionally. For example, in the manufacture of semiconductor devices it Is common to deposit a photoresist material onto a substrate to form a mask for the etching operation and to subsequently remove the .. photoresist material from the substrate. The term "contaminant" as used herein is intended to cover and encompass such a photo resist material. .
Preferred methods of the present invention comprise applying the present composition to the article, with vapor degreasing and solvent cleaning methods being particularly preferred for certain applications, especially those intricate parts and difficult to remove soils. Preferred vapor degreasing and solvent cleaning methods consist of exposing an article, preferably at room-temperature, to the vapors of a boiling solvent Vapors condensing on the object have the advantage of providing a relatively clean, distilled solvent to wash away grease or other contamination. Such processes thus have an additional advantage in that final evaporation of the present solvent composition from the object leaves behind relatively little residue as compared to the case where the object is simply washed in liquid solvent For applications in which the article includes contaminants that are difficult to remove, it is preferred that the present methods involve raising the temperature of .. the solvent composition of the present Invention above ambient or to any other temperature that is effective in such application to substantially improve the cleaning action of the solvent Such processes are also generally preferred for large volume =
may be combined with the corm:monism in a conventional manner to produce rigid foams.
CLEANING METHODS
The present invention also provides methods of removing containments from a product, part, component, substrate, or any other article or portion thereof by applying to the article a composition of the present invention. For the purposes of convenience, the term "article" is used herein to refer to all such products, parts, components, substrates, and the like and is further intended to refer to any surface or portion thereof. Furthermore, the term "contaminant" is Intended to refer to any unwanted material or substance present on the article, even if such substance is placed on the article intentionally. For example, in the manufacture of semiconductor devices it Is common to deposit a photoresist material onto a substrate to form a mask for the etching operation and to subsequently remove the .. photoresist material from the substrate. The term "contaminant" as used herein is intended to cover and encompass such a photo resist material. .
Preferred methods of the present invention comprise applying the present composition to the article, with vapor degreasing and solvent cleaning methods being particularly preferred for certain applications, especially those intricate parts and difficult to remove soils. Preferred vapor degreasing and solvent cleaning methods consist of exposing an article, preferably at room-temperature, to the vapors of a boiling solvent Vapors condensing on the object have the advantage of providing a relatively clean, distilled solvent to wash away grease or other contamination. Such processes thus have an additional advantage in that final evaporation of the present solvent composition from the object leaves behind relatively little residue as compared to the case where the object is simply washed in liquid solvent For applications in which the article includes contaminants that are difficult to remove, it is preferred that the present methods involve raising the temperature of .. the solvent composition of the present Invention above ambient or to any other temperature that is effective in such application to substantially improve the cleaning action of the solvent Such processes are also generally preferred for large volume =
13 =
assembly One operations where the cleaning of the article, particularly metal parts and assemblies, must be done efficiently and quickly.
In preferred embodiments, the cleaning methods of the present invention comprise immersing the article to be cleaned in liquid solvent al an elevated temperature, and even more preferably at about the boiling point of the solvent In such operations, this step preferably removes a substantial amount, and evert more preferably a major portion, of the target contaminant from the article. This step Is then preferably followed by immersing the article in solvent, preferably freshly distilled solvent, which is at a temperature below the temperature of the liquid solVent in the preceding immersion step, preferably at about ambient or room temperature.
The preferred methods also include the step of then contacting the article with relatively hot vapor of the present solvent composition, preferably by exposing the article to solvent vapors rising from the hot/boiling solvent associated with the first mentioned immersion step. This preferably results in condensation of the solvent .. vapor on the article. In certain preferred embodiments, the article may be sprayed with distilled solvent before final rinsing.
It is contemplated that numerous varieties and types of vapor degreasing = equipment are adaptable for use in connection with the present methods.
One example of such equipment and its operation is disclosed by Sherliker et al.
in U.S.
Pat No. 3,085,918. The equipment = =
disclosed in Sherliker et al Includes a boiling sump for containing a solvent composition, a dean sump for containing disblied solvent, a water separator, and other ancillary equipment The present cleaning methods may also comprise cold cleaning in which the contaminated article is either immersed in the fluid composition of the present Invention under ambient or room temperature conditions or wiped under such conditions with rags or similar objects soaked In solvents.
=
FLAMMABIIJTY REDUCTION METHODS
According to certain other preferred embodiments, the present invention provides methods for reducing the flammability of fluids, said methods comprising .
assembly One operations where the cleaning of the article, particularly metal parts and assemblies, must be done efficiently and quickly.
In preferred embodiments, the cleaning methods of the present invention comprise immersing the article to be cleaned in liquid solvent al an elevated temperature, and even more preferably at about the boiling point of the solvent In such operations, this step preferably removes a substantial amount, and evert more preferably a major portion, of the target contaminant from the article. This step Is then preferably followed by immersing the article in solvent, preferably freshly distilled solvent, which is at a temperature below the temperature of the liquid solVent in the preceding immersion step, preferably at about ambient or room temperature.
The preferred methods also include the step of then contacting the article with relatively hot vapor of the present solvent composition, preferably by exposing the article to solvent vapors rising from the hot/boiling solvent associated with the first mentioned immersion step. This preferably results in condensation of the solvent .. vapor on the article. In certain preferred embodiments, the article may be sprayed with distilled solvent before final rinsing.
It is contemplated that numerous varieties and types of vapor degreasing = equipment are adaptable for use in connection with the present methods.
One example of such equipment and its operation is disclosed by Sherliker et al.
in U.S.
Pat No. 3,085,918. The equipment = =
disclosed in Sherliker et al Includes a boiling sump for containing a solvent composition, a dean sump for containing disblied solvent, a water separator, and other ancillary equipment The present cleaning methods may also comprise cold cleaning in which the contaminated article is either immersed in the fluid composition of the present Invention under ambient or room temperature conditions or wiped under such conditions with rags or similar objects soaked In solvents.
=
FLAMMABIIJTY REDUCTION METHODS
According to certain other preferred embodiments, the present invention provides methods for reducing the flammability of fluids, said methods comprising .
14 adding a compound or composition of the present invention to said fluid. The flammability associated with any of a wide range of otherwise flammable fluids may be reduced according to the present invention. For example, the flammability associated with fluids such as ethylene oxide, flammable hydrofluorocarbons and hydrocarbons. including: HFC-152a, 1.1.1-trifluoroethane (HFC-143a), dfluoromethane (HFC-32), propane, hexane, octane, and the like can be reduced according to the present invention. For the purposes of the present invention, a flammable fluid.may be any fluid exhibiting flammability ranges in air as measured via any standard conventional test method, such as ASTIVI E-681.. and the like.
Any suitable amounts of the present compounds or compositions may be added to reduce flammability of a fluid according to the present invention. As will be recognized by those of skill in the art, the amount added will depend, at least in part, on the degree to which the subject fluid is flammable and the degree to which it is desired to reduce the flammability thereof. In certain preferred embodiment's, the amount of compound or composition added to the flammable fluid is effective to render the resulting fluid substantially non-flammable.
FLAME SUPPRESSION METHODS
The present invention further provides methods of suppressing a flame, said methods comprising contacting a flame with a fluid comprising a compound or composition of the present invention. Any suitable methods for contacting the flame with the present composition may be used. For example, a composition of the present invention may be sprayed, poured, and the like onto the flame, or at least a portion of the flame may be immersed in the composition. In light of the teachings herein, those of akal in the art will be readily able to adapt a variety of conventional = apparatus and methods of flame suppression for use in the present invention.
STERILIZA'710N METHODS
Many articles, devices and materials, particularly for use in the medical field, must be sterilized prior to use for the health and safety reasons, such as the health and safety of patients and hospital staff. The present invention provides methods of sterilizing comprising contacting the articles, devices or material to be sterilized with a compound or composition of the present invention. Such methods may be either high or low-temperature sterilization methods. In certain embodiments, high-temperature sterilization comprises exposing the articles, device or material to be sterilized to a hot fluid comprising a compound or composition of the present invention at a temperature of from about 250 F to about 270 F, preferably in a substantially sealed chamber. The process can be completed usually in less than.
about 2 hours. However, some articles, such as plastic articles and electrical .. components, cannot withstand such high temperatures and require low-temperature sterilization.
Low-temperature sterilization of the present invention involves the use of a compound or composition of the present invention at a temperature of from about 100 to about 200 F. The compounds of the present invention may be combined with .. other common chemical steritants, including, for example, ethylene oxide (EO).
formaldehyde, hydrogen peroxide, chlorine dioxide, and ozone to form a sterilant composition of the present invention.
The low-temperature sterilization of the present invention is preferably at least a two-step process performed in a substantially sealed, preferably air tight.
chamber.
.. In the first step (the sterilization step), the articles having been cleaned and wrapped in gas permeable bags are placed in the chamber. Air is then evacuated from the -chamber by pulling a vacuum and perhaps by displacing the air with steam. In certain embodiments, it is preferable to inject steam into the chamber to achieve a relative humidity that ranges preferably from about 30% to about 70%. Such humidities may maximize the sterilizing effectiveness of the sterilant which is introduced into the chamber after the desired relative humidity is achieved..
After a period of time sufficient for the sterilant to permeate the wrapping and reach the interstices of the article, the sterilant and steam are evacuated from the chamber.
In the preferred second step of the process (the aeration step), the articles are . 30 aerated to.remove sterilant residues. Removing such residues is particularly important in the case of toxic sterilants, although it is optional in those cases in which =
the substantially non-toxic compounds of the present invention are used.
Typical aeration processes Include air washes, continuous aeration, and a combination of the two. An air wash is a batch process and usually comprises evacuating the chamber for a relatively short period, for example, 12 minutes, and then Introducing air at atmospheric pressure or higher into the chamber. This cycle is repeated any number of times until the desired removal of sterilant is achieved. Continuous aeration typically Involves introducing air through an inlet at one side of the chamber and then drawirt it out through an outlet on the other side of the chamber by =
applying a slight vacuum to the outlet Frequently, the two approaches are combined. For example, a common approach involves performing air washes and then an aeration cycle.
EXAMPLES
The following examples are provided for the purpose of illustrating the present invention but without limiting the scope thereof.
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 amount of cooling or heating it provides and provides some measure of the capability of a compressor to pump quantities of heat for a given volumetric Bow rate of refrigerant.
In other lords, 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 lair conditioning cycle system Is provided where the condenser temperature is about 150*F and the evaporator temperature Is about -35*F under nominally isentropic 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
=
REFRIGERANT Relative COP Relative DISCHARGE
COMPOSTION CAPACITY TEMPERATURE
(F) _HFO 1225ve 1.02 Ql FOtre_m_12.U.L. e jQ4 0,70 165 HFO 1234vf 0 98iiQ 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.
The miscibility of HF0-1225ye and HF0-1234ze 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 * Trade-mark , =
, .
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 UFO-1225ye mixtures with polyalkylene glycol, the refrigerant mixture was found to be immiscible over the temperature range of-50C 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 The e 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 tasted 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 al 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) HFC1243 zf and GM Goodwrench oil PAG oil HFC-1234ze and MOPAR-56 PAG oil =
=
d) HFC-1243 zf 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.
Any suitable amounts of the present compounds or compositions may be added to reduce flammability of a fluid according to the present invention. As will be recognized by those of skill in the art, the amount added will depend, at least in part, on the degree to which the subject fluid is flammable and the degree to which it is desired to reduce the flammability thereof. In certain preferred embodiment's, the amount of compound or composition added to the flammable fluid is effective to render the resulting fluid substantially non-flammable.
FLAME SUPPRESSION METHODS
The present invention further provides methods of suppressing a flame, said methods comprising contacting a flame with a fluid comprising a compound or composition of the present invention. Any suitable methods for contacting the flame with the present composition may be used. For example, a composition of the present invention may be sprayed, poured, and the like onto the flame, or at least a portion of the flame may be immersed in the composition. In light of the teachings herein, those of akal in the art will be readily able to adapt a variety of conventional = apparatus and methods of flame suppression for use in the present invention.
STERILIZA'710N METHODS
Many articles, devices and materials, particularly for use in the medical field, must be sterilized prior to use for the health and safety reasons, such as the health and safety of patients and hospital staff. The present invention provides methods of sterilizing comprising contacting the articles, devices or material to be sterilized with a compound or composition of the present invention. Such methods may be either high or low-temperature sterilization methods. In certain embodiments, high-temperature sterilization comprises exposing the articles, device or material to be sterilized to a hot fluid comprising a compound or composition of the present invention at a temperature of from about 250 F to about 270 F, preferably in a substantially sealed chamber. The process can be completed usually in less than.
about 2 hours. However, some articles, such as plastic articles and electrical .. components, cannot withstand such high temperatures and require low-temperature sterilization.
Low-temperature sterilization of the present invention involves the use of a compound or composition of the present invention at a temperature of from about 100 to about 200 F. The compounds of the present invention may be combined with .. other common chemical steritants, including, for example, ethylene oxide (EO).
formaldehyde, hydrogen peroxide, chlorine dioxide, and ozone to form a sterilant composition of the present invention.
The low-temperature sterilization of the present invention is preferably at least a two-step process performed in a substantially sealed, preferably air tight.
chamber.
.. In the first step (the sterilization step), the articles having been cleaned and wrapped in gas permeable bags are placed in the chamber. Air is then evacuated from the -chamber by pulling a vacuum and perhaps by displacing the air with steam. In certain embodiments, it is preferable to inject steam into the chamber to achieve a relative humidity that ranges preferably from about 30% to about 70%. Such humidities may maximize the sterilizing effectiveness of the sterilant which is introduced into the chamber after the desired relative humidity is achieved..
After a period of time sufficient for the sterilant to permeate the wrapping and reach the interstices of the article, the sterilant and steam are evacuated from the chamber.
In the preferred second step of the process (the aeration step), the articles are . 30 aerated to.remove sterilant residues. Removing such residues is particularly important in the case of toxic sterilants, although it is optional in those cases in which =
the substantially non-toxic compounds of the present invention are used.
Typical aeration processes Include air washes, continuous aeration, and a combination of the two. An air wash is a batch process and usually comprises evacuating the chamber for a relatively short period, for example, 12 minutes, and then Introducing air at atmospheric pressure or higher into the chamber. This cycle is repeated any number of times until the desired removal of sterilant is achieved. Continuous aeration typically Involves introducing air through an inlet at one side of the chamber and then drawirt it out through an outlet on the other side of the chamber by =
applying a slight vacuum to the outlet Frequently, the two approaches are combined. For example, a common approach involves performing air washes and then an aeration cycle.
EXAMPLES
The following examples are provided for the purpose of illustrating the present invention but without limiting the scope thereof.
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 amount of cooling or heating it provides and provides some measure of the capability of a compressor to pump quantities of heat for a given volumetric Bow rate of refrigerant.
In other lords, 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 lair conditioning cycle system Is provided where the condenser temperature is about 150*F and the evaporator temperature Is about -35*F under nominally isentropic 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
=
REFRIGERANT Relative COP Relative DISCHARGE
COMPOSTION CAPACITY TEMPERATURE
(F) _HFO 1225ve 1.02 Ql FOtre_m_12.U.L. e jQ4 0,70 165 HFO 1234vf 0 98iiQ 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.
The miscibility of HF0-1225ye and HF0-1234ze 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 * Trade-mark , =
, .
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 UFO-1225ye mixtures with polyalkylene glycol, the refrigerant mixture was found to be immiscible over the temperature range of-50C 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 The e 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 tasted 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 al 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) HFC1243 zf and GM Goodwrench oil PAG oil HFC-1234ze and MOPAR-56 PAG oil =
=
d) HFC-1243 zf 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 (13)
1. Use of a composition comprising 1,3,3,3-tetrafluoropropene (HFO-1234ze) as a propellant.
2. Use according to claim 1, wherein the composition is not an azeotrope-like composition consisting essentially of trans-1,3,3,3-tetrafluoropropene (transHFO-1234ze) and a compound selected from 1,1-difluoroethane ("HFC-152a"), 1,1,1,2,3,3,3-heptafluoropropane ("HFC-227ea"), 1,1,1,2-tetrafluorethane ("HFC-134a"), or 1,1,1,2,2-pentafluoroethane ("HFC-125").
3. Use of a composition comprising 2,3,3,3-tetrafluoropropene (HFO-1234yf) as a propellant.
4. Use according to any one of claims 1 to 3, wherein the composition is a sprayable composition.
5. Use according to claim 4, wherein the sprayable composition is an aerosol.
6. Use according to any one of claims 4 or 5, wherein the composition further comprises one or more of inert ingredients and solvents.
7. A sprayable composition comprising 1,3,3,3-tetrafluoropropene (HFO-1234ze) and a material to be sprayed.
8. A sprayable composition according to claim 7, wherein the composition is not an azeotrope-like composition consisting essentially of trans-1,3,3,3-tetrafluoropropene (transHFO-1234ze) and a compound selected from 1,1-difluoroethane ("HFC-152a"), 1,1,1,2,3,3,3-heptafluoropropane ("HFC-227ea"), 1,1,1,2-tetrafluorethane ("HFC-134a"), or 1,1,1,2,2-pentafluoroethane ("HFC-125").
9. A sprayable composition comprising 2,3,3,3-tetrafluoropropene (HFO-1234yf) and a material to be sprayed.
10. A sprayable composition according to any one of claims 7 to 9, wherein the material to be sprayed comprises a cosmetic material or a medicinal material.
11. A sprayable composition according to claim 10, wherein the cosmetic material is selected from the group consisting of deodorants, perfumes, hair sprays, cleansers and polishing agents.
12. A sprayable composition according to claim 11, wherein the medicinal material is selected from the group consisting of anti-asthma and anti-halitosis medications.
13. A sprayable composition according to any one of claims 7 to 12, wherein the composition is an aerosol.
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US42126302P | 2002-10-25 | 2002-10-25 | |
US42143502P | 2002-10-25 | 2002-10-25 | |
US60/421,263 | 2002-10-25 | ||
US60/421,435 | 2002-10-25 | ||
CA2927535A CA2927535C (en) | 2002-10-25 | 2003-10-27 | Compositions containing fluorine substituted olefins |
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CA2826545A Expired - Fee Related CA2826545C (en) | 2002-10-25 | 2003-10-27 | Compositions containing fluorine substituted olefins |
CA2927535A Expired - Lifetime CA2927535C (en) | 2002-10-25 | 2003-10-27 | Compositions containing fluorine substituted olefins |
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CA2927535A Expired - Lifetime CA2927535C (en) | 2002-10-25 | 2003-10-27 | Compositions containing fluorine substituted olefins |
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CN (1) | CN106118603A (en) |
CA (3) | CA3054717C (en) |
ES (1) | ES2357937T5 (en) |
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CN116285306B (en) * | 2023-05-24 | 2023-08-18 | 北京宇极科技发展有限公司 | Foaming composition, polyurethane foam and preparation method thereof |
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US3884828A (en) * | 1970-10-15 | 1975-05-20 | Dow Corning | Propellants and refrigerants based on trifluoropropene |
JPH04110388A (en) * | 1990-08-31 | 1992-04-10 | Daikin Ind Ltd | Fluid for heat transfer |
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2003
- 2003-10-27 SI SI200332152T patent/SI1563032T1/en unknown
- 2003-10-27 ES ES10006819T patent/ES2357937T5/en not_active Expired - Lifetime
- 2003-10-27 CN CN201610414066.4A patent/CN106118603A/en active Pending
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- 2003-10-27 PT PT08020700T patent/PT2036943E/en unknown
- 2003-10-27 CA CA2826545A patent/CA2826545C/en not_active Expired - Fee Related
- 2003-10-27 CA CA2927535A patent/CA2927535C/en not_active Expired - Lifetime
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PT2036943E (en) | 2011-09-22 |
CN106118603A (en) | 2016-11-16 |
CA2826545C (en) | 2018-02-20 |
CA2826545A1 (en) | 2004-05-06 |
SI1563032T1 (en) | 2012-07-31 |
SI2314654T1 (en) | 2016-12-30 |
SI2036943T1 (en) | 2011-12-30 |
CA2927535A1 (en) | 2004-05-06 |
CA2927535C (en) | 2021-01-12 |
ES2357937T5 (en) | 2021-07-21 |
ES2357937T3 (en) | 2012-02-29 |
ES2357937T1 (en) | 2011-05-04 |
CA3054717C (en) | 2020-12-15 |
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