WO1993006187A1 - Refrigerant and refrigerator - Google Patents
Refrigerant and refrigerator Download PDFInfo
- Publication number
- WO1993006187A1 WO1993006187A1 PCT/JP1992/001216 JP9201216W WO9306187A1 WO 1993006187 A1 WO1993006187 A1 WO 1993006187A1 JP 9201216 W JP9201216 W JP 9201216W WO 9306187 A1 WO9306187 A1 WO 9306187A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- refrigerant
- present
- refrigerator
- ozone
- hexafluorobutane
- Prior art date
Links
- 239000003507 refrigerant Substances 0.000 title claims abstract description 30
- CXIGIYYQHHRBJC-UHFFFAOYSA-N 1,1,1,4,4,4-hexafluorobutane Chemical compound FC(F)(F)CCC(F)(F)F CXIGIYYQHHRBJC-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000001875 compounds Chemical class 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920001515 polyalkylene glycol Polymers 0.000 description 3
- 238000005057 refrigeration Methods 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 238000005422 blasting Methods 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- ZQBFAOFFOQMSGJ-UHFFFAOYSA-N hexafluorobenzene Substances FC1=C(F)C(F)=C(F)C(F)=C1F ZQBFAOFFOQMSGJ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- HXITXNWTGFUOAU-UHFFFAOYSA-N phenylboronic acid Chemical compound OB(O)C1=CC=CC=C1 HXITXNWTGFUOAU-UHFFFAOYSA-N 0.000 description 2
- 239000005437 stratosphere Substances 0.000 description 2
- WXGNWUVNYMJENI-UHFFFAOYSA-N 1,1,2,2-tetrafluoroethane Chemical compound FC(F)C(F)F WXGNWUVNYMJENI-UHFFFAOYSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- CYXIKYKBLDZZNW-UHFFFAOYSA-N 2-Chloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)CCl CYXIKYKBLDZZNW-UHFFFAOYSA-N 0.000 description 1
- QJYKUYUDWYBTAI-UHFFFAOYSA-N C=1C=CC=CC=1OBOC1=CC=CC=C1 Chemical compound C=1C=CC=CC=1OBOC1=CC=CC=C1 QJYKUYUDWYBTAI-UHFFFAOYSA-N 0.000 description 1
- XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical compound FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- 101001083543 Homo sapiens Host cell factor 1 Proteins 0.000 description 1
- 102100030355 Host cell factor 1 Human genes 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- RAVYCAKJPSRHHO-UHFFFAOYSA-N OP(O)(=O)OP(=O)(O)OP(=O)(O)O.Cl.Cl.Cl Chemical class OP(O)(=O)OP(=O)(O)OP(=O)(O)O.Cl.Cl.Cl RAVYCAKJPSRHHO-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- RWRIWBAIICGTTQ-UHFFFAOYSA-N anhydrous difluoromethane Natural products FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- -1 chlorine radicals Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- ACYQYBAHTSKBLM-UHFFFAOYSA-N difluoromethoxy(trifluoro)methane Chemical compound FC(F)OC(F)(F)F ACYQYBAHTSKBLM-UHFFFAOYSA-N 0.000 description 1
- CZHYKKAKFWLGJO-UHFFFAOYSA-N dimethyl phosphite Chemical compound COP([O-])OC CZHYKKAKFWLGJO-UHFFFAOYSA-N 0.000 description 1
- KUMNEOGIHFCNQW-UHFFFAOYSA-N diphenyl phosphite Chemical compound C=1C=CC=CC=1OP([O-])OC1=CC=CC=C1 KUMNEOGIHFCNQW-UHFFFAOYSA-N 0.000 description 1
- NFORZJQPTUSMRL-UHFFFAOYSA-N dipropan-2-yl hydrogen phosphite Chemical compound CC(C)OP(O)OC(C)C NFORZJQPTUSMRL-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 150000002220 fluorenes Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000010721 machine oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000004971 nitroalkyl group Chemical group 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- XEIJMVGQZDKEPZ-UHFFFAOYSA-N perfluoroethanamine Chemical compound FN(F)C(F)(F)C(F)(F)F XEIJMVGQZDKEPZ-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- WSANLGASBHUYGD-UHFFFAOYSA-N sulfidophosphanium Chemical class S=[PH3] WSANLGASBHUYGD-UHFFFAOYSA-N 0.000 description 1
- 238000004781 supercooling Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- XPDWGBQVDMORPB-UHFFFAOYSA-N trifluoromethane acid Natural products FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 1
- KTFAZNVGJUIWJM-UHFFFAOYSA-N trimethyl(sulfanylidene)-$l^{5}-phosphane Chemical compound CP(C)(C)=S KTFAZNVGJUIWJM-UHFFFAOYSA-N 0.000 description 1
- MDCWDBMBZLORER-UHFFFAOYSA-N triphenyl borate Chemical compound C=1C=CC=CC=1OB(OC=1C=CC=CC=1)OC1=CC=CC=C1 MDCWDBMBZLORER-UHFFFAOYSA-N 0.000 description 1
- VYNGFCUGSYEOOZ-UHFFFAOYSA-N triphenylphosphine sulfide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=S)C1=CC=CC=C1 VYNGFCUGSYEOOZ-UHFFFAOYSA-N 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 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
- 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
-
- 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
- C09K2205/00—Aspects relating to compounds used in compression type refrigeration systems
- C09K2205/24—Only one single fluoro component present
Definitions
- the present invention relates to a novel refrigerant and a refrigerator using the refrigerant.
- chlorofluoroalkanes As the working fluid or refrigerant, chlorofluoroalkanes, azeotropic compositions thereof, and compositions having compositions in the vicinity thereof have been known.
- the working fluids for refrigerators currently include CFC 11 (tri-fluoro fluorometer), CFC 12 (dichloro ⁇ difluorometer), and CFC 114 (1, 2).
- CFC 11 tri-fluoro fluorometer
- CFC 12 diichloro ⁇ difluorometer
- CFC 114 (1, 2).
- HCFC22 Chlorofluoromethane
- HCFC22 has an ozone destruction coefficient (hereinafter referred to as ODP) which is considerably lower than that of the above-mentioned regulated compounds (for example, about 1Z20 of CFC11). Although not covered, it is hoped that compounds with zero DP will be replaced in the future.
- ODP ozone destruction coefficient
- a chlorofluoroalkane or a fluoroanolecan containing a hydrogen atom for example, HCFC 2 1 (monochrome monofluorometer), HFC23 (trifluorometer), HFC32 (difluorometer), HCFC124 (monochrome trafluorometer), HFC1 2 5 (Pentafull ), HCFC 133a (monochrome trifluorene), HFC134a (tetrafluorene), HCFC144b (monochrome fluorene), HFC143a (Trifluorene).
- the main purpose of the present invention is to provide a refrigerant having 0 D D which is zero, has excellent performance as a refrigerant, and does not substantially undergo a composition change upon phase change during equipment operation. .
- the present inventor has conducted various studies in view of the current state of the technology as described above. As a result, we found that 1,1,1,4,4,4-hexafluorobenzene had the requirements to meet its purpose.
- the present invention provides a refrigerant comprising 1,1,1,4,4,4-hexafluorobenzene.
- the present invention provides a refrigerator using 1,1,1,4,4,4-hexafluorobutane as a refrigerant.
- the refrigerant of the present invention can optionally contain a stabilizer. That is, when a high degree of stability is required under severe use conditions, the following stabilizers can be blended.
- Phosphites such as dimethyl phosphite, diisopropyl phosphite and diphenyl phosphite;
- triphosphorites such as trichloride triphosphates
- phosphine sulfides such as triphenyl phosphine sulfide and trimethyl phosphine sulfide
- 6-phenols such as t-tert-butylparacresol
- Nitroalkanes such as nitromethane and nitroethane
- acrylates such as methyl monoacrylate and ethyl acrylate
- These stabilizers are usually added at a ratio of about 0.01 to 5% of the weight of the refrigerant.
- ethers such as dimethyl ether and pentafluorodimethyl ether
- amines such as perfluoroethylamine
- the 1,1,1,1,4,4,4-hexafluorobutane used in the present invention is easily decomposable and does not contain chlorine atoms that affect the ozone layer, so that the ODP is zero and the ozone layer There is no danger of causing blasting problems.
- the refrigerant according to the present invention has a relatively good refrigerating capacity of about 80% as compared with CFC11, and has the same coefficient of performance. Demonstrate overall superior performance. Therefore, it can be replaced with CFC11, which is currently used as a turbo refrigerant.
- the refrigerant according to the present invention is composed of a single compound, liquid management, reuse after recovery, and the like can be advantageously performed.
- the refrigerant according to the present invention has low solubility in a polymer compound, it can be used as it is without changing the material in an existing refrigerator.
- the refrigerant according to the present invention has excellent compatibility with PAG (polyalkylene glycol) -based oils, polyester-based oils, and the like.
- the refrigerant according to the present invention is nonflammable and has good thermal stability.
- the evaporation temperature of the refrigerant in the condenser is set at 5 ° C
- the condensation temperature is set at 40 ° C
- the superheat temperature at the inlet of the compressor is set at 10 ° C.
- the operation was performed with the degree of supercooling at the condenser outlet at 5 ° C.
- Polyalkylene glycol is used as refrigerating machine oil did
- Table 2 shows the coefficient of performance (COP), refrigeration capacity [kcal / m "] and compressor gas discharge temperature (in) .Table 2 shows the results for CFC 11 as a comparison. Table 2
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
- Devices That Are Associated With Refrigeration Equipment (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3245935A JPH0585966A (ja) | 1991-09-25 | 1991-09-25 | 冷 媒 |
JP3/245935 | 1991-09-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1993006187A1 true WO1993006187A1 (en) | 1993-04-01 |
Family
ID=17141051
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1992/001216 WO1993006187A1 (en) | 1991-09-25 | 1992-09-25 | Refrigerant and refrigerator |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0558763A4 (ja) |
JP (1) | JPH0585966A (ja) |
WO (1) | WO1993006187A1 (ja) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5562855A (en) * | 1994-09-29 | 1996-10-08 | E. I. Du Pont De Nemours And Company | Octafluorobutane compositions |
US5688431A (en) * | 1994-09-29 | 1997-11-18 | E. I. Du Pont De Nemours And Company | Octafluorobutane compositions |
US20070098646A1 (en) | 2005-11-01 | 2007-05-03 | Nappa Mario J | Aerosol propellants comprising unsaturated fluorocarbons |
EP3567092A1 (en) | 2005-11-01 | 2019-11-13 | The Chemours Company FC, LLC | Solvent compositions comprising unsaturated fluorinated hydrocarbons |
US7972524B2 (en) | 2007-04-27 | 2011-07-05 | E. I. Du Pont De Nemours And Company | Azeotropic and azeotrope-like compositions of Z-1,1,1,4,4,4-hexafluoro-2-butene |
CN103980521B (zh) * | 2007-06-12 | 2016-11-23 | 纳幕尔杜邦公司 | E-1,1,1,4,4,4-六氟-2-丁烯的共沸和类共沸组合物 |
MX2010002471A (es) | 2007-09-06 | 2010-03-26 | Du Pont | Composiciones azeotropicas y similares a azeotropos de e-1,1,1,4,4,5,5,5-octafluoro-2-penteno. |
EP2215154B1 (en) | 2007-11-29 | 2017-12-20 | The Chemours Company FC, LLC | Compositions and use of cis-1,1,1,4,4,4-hexafluoro-2-butene foam-forming composition in the preparation of polyisocyanate-based foams |
CA2708274C (en) | 2007-12-19 | 2016-10-18 | E. I. Du Pont De Nemours And Company | Foam-forming compositions containing azeotropic or azeotrope-like mixtures containing z-1,1,1,4,4,4-hexafluoro-2-butene and their uses in the preparation of polyisocyanate-based foams |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01146831A (ja) * | 1987-10-20 | 1989-06-08 | Bayer Ag | フツ素化c↓4〜c↓6炭化水素の製造方法 |
JPH0229440A (ja) * | 1988-06-01 | 1990-01-31 | Bayer Ag | 発泡プラスチツクの製造用の膨張かつ絶縁ガスとしての1,1,1,4,4,4―ヘキサフルオロブタンの使用 |
-
1991
- 1991-09-25 JP JP3245935A patent/JPH0585966A/ja active Pending
-
1992
- 1992-09-25 WO PCT/JP1992/001216 patent/WO1993006187A1/ja not_active Application Discontinuation
- 1992-09-25 EP EP19920920355 patent/EP0558763A4/en not_active Withdrawn
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01146831A (ja) * | 1987-10-20 | 1989-06-08 | Bayer Ag | フツ素化c↓4〜c↓6炭化水素の製造方法 |
JPH0229440A (ja) * | 1988-06-01 | 1990-01-31 | Bayer Ag | 発泡プラスチツクの製造用の膨張かつ絶縁ガスとしての1,1,1,4,4,4―ヘキサフルオロブタンの使用 |
Non-Patent Citations (1)
Title |
---|
See also references of EP0558763A4 * |
Also Published As
Publication number | Publication date |
---|---|
JPH0585966A (ja) | 1993-04-06 |
EP0558763A4 (en) | 1993-10-06 |
EP0558763A1 (en) | 1993-09-08 |
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