WO1993010203A1 - Refrigerant comprenant de l'octafluorobutane - Google Patents
Refrigerant comprenant de l'octafluorobutane Download PDFInfo
- Publication number
- WO1993010203A1 WO1993010203A1 PCT/JP1992/001502 JP9201502W WO9310203A1 WO 1993010203 A1 WO1993010203 A1 WO 1993010203A1 JP 9201502 W JP9201502 W JP 9201502W WO 9310203 A1 WO9310203 A1 WO 9310203A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- refrigerant
- chf
- present
- chfcf
- group
- Prior art date
Links
- 239000003507 refrigerant Substances 0.000 title claims abstract description 63
- 150000001875 compounds Chemical class 0.000 abstract description 10
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 abstract 2
- 108010081348 HRT1 protein Hairy Proteins 0.000 abstract 2
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 abstract 2
- YUCFVHQCAFKDQG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH] YUCFVHQCAFKDQG-UHFFFAOYSA-N 0.000 description 25
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 11
- 230000006378 damage Effects 0.000 description 7
- 238000009834 vaporization Methods 0.000 description 6
- 230000008016 vaporization Effects 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 5
- RWRIWBAIICGTTQ-UHFFFAOYSA-N anhydrous difluoromethane Natural products FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 229920001515 polyalkylene glycol Polymers 0.000 description 3
- 238000005057 refrigeration Methods 0.000 description 3
- XPDWGBQVDMORPB-UHFFFAOYSA-N trifluoromethane acid Natural products FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 3
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- -1 chlorine radicals Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000005437 stratosphere Substances 0.000 description 2
- ZXUJWPHOPHHZLR-UHFFFAOYSA-N 1,1,1-trichloro-2-fluoroethane Chemical compound FCC(Cl)(Cl)Cl ZXUJWPHOPHHZLR-UHFFFAOYSA-N 0.000 description 1
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- JQZFYIGAYWLRCC-UHFFFAOYSA-N 1-chloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)C(F)(F)Cl JQZFYIGAYWLRCC-UHFFFAOYSA-N 0.000 description 1
- BHNZEZWIUMJCGF-UHFFFAOYSA-N 1-chloro-1,1-difluoroethane Chemical compound CC(F)(F)Cl BHNZEZWIUMJCGF-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
- JJXBITPDOUWVAI-UHFFFAOYSA-N Bc1ccc(F)c(F)c1F Chemical compound Bc1ccc(F)c(F)c1F JJXBITPDOUWVAI-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
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-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
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- CZHYKKAKFWLGJO-UHFFFAOYSA-N dimethyl phosphite Chemical compound COP([O-])OC CZHYKKAKFWLGJO-UHFFFAOYSA-N 0.000 description 1
- OGGXGZAMXPVRFZ-UHFFFAOYSA-N dimethylarsinic acid Chemical compound C[As](C)(O)=O OGGXGZAMXPVRFZ-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
- 238000005516 engineering process Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000010721 machine oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 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
- 150000002924 oxiranes Chemical class 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
- 150000002989 phenols Chemical class 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-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
- 230000002000 scavenging 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
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 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
- SJHCUXCOGGKFAI-UHFFFAOYSA-N tripropan-2-yl phosphite Chemical compound CC(C)OP(OC(C)C)OC(C)C SJHCUXCOGGKFAI-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
- 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
- C09K2205/22—All components of a mixture being fluoro compounds
Definitions
- Refrigerant consisting of octafluorobenzene
- the present invention relates to a novel refrigerant.
- a working fluid or a refrigerant As a working fluid or a refrigerant, a chlorofluoroalkane, an azeotropic composition thereof, and a composition having a composition in the vicinity thereof have been known.
- the working fluids for refrigerators at present are CFC11 (trichlorofluorometer), CFC12 (dichlorodifluorometer) and CFC114.
- New paper Demand is increasing year by year due to the spread of air conditioning and refrigeration equipment. Restrictions on the use and production of these refrigerants have been imposed by all current social organizations, including living environments, food storage and transportation. Due to its large impact on the public, the development of new refrigerants that have no or very low risk of causing ozone depletion has become an urgent issue.
- Promising compounds that can be substituted for the above-mentioned chlorofluoroalkanes include chlorofluoroalkanes or fluoroalkanes containing a hydrogen atom, such as HCFC21 Fluoromethane), HFC23 (Trifluoromethane), HFC32 (Difluoromethane), HCFC123 (Trichlorofluoroethane), HCFC124 (Monochlorotetrafluoroethane), HFC125 (Pentafluoroethan), HCFC13a (monochlorotrifluoroethane), HFC134a (tetrafluorene), HCFC144b (monochlorodifluoroethane), HFC143 a (trifluo).
- chlorofluoroalkanes or fluoroalkanes containing a hydrogen atom such as HCFC21 Fluoromethane), HFC23 (Trifluoromethane), HFC32 (Difluoromethan
- HCFC123 is an ODP It is not much regulated (e.g., about 1Z50 for CFC 11), but may be more toxic than CFC 11 and may have 0 DP in the future. It is hoped that this will be replaced by a compound from Zeguchi.
- the present invention provides a refrigerant that has low toxicity to the human body, has zero ODP, has excellent performance as a refrigerant, and does not substantially involve a change in composition during a phase change during equipment operation. Is the main purpose.
- the present inventor has conducted various studies in view of the above-mentioned state of the art. As a result, they have found that a refrigerant composed of a fluorinated hydrocarbon having a specific structure has requirements meeting its purpose.
- the present invention provides CF n CF 2 CH 2 CF 3 (1,1,1,2,2,4,4,4-octanol phenol) and CF 3 CH (CHF 2 ) CF n (2— Difluoromethyl-1,1,1,3,3,3—tetrafluoroprono.
- CHF 2 CF (CHF 2 ) provides a refrigerant selected from the group consisting of CF 3 (2-difluoromethyl—1,1,2,3,3,3-tetrafluoropropane). 0
- the present invention relates to CF 3 CF 2 CH. CF 3 ⁇
- An object of the present invention is to provide a refrigerator that operates using one type of refrigerant selected from the group consisting of:
- the present invention relates to CF. CF 2 CH £ CF 3 ,
- CHF 2 CF (CHF 2 ) provides use as one type of refrigerant selected from the group consisting of CF 3 .
- Preferred refrigerants used in the present invention include CF 3 CF 2 CH 2 CF 3 , CF ⁇ CH (CHF £ ) ⁇ , and CF.
- C New paper Four types of HFCF 2 CHF 2 and CF 3 CF 2 CF 2 CH 2 F are mentioned.
- the refrigerant of the present invention may contain another refrigerant to such an extent that its performance is not impaired.
- the six types of fluorinated hydrocarbons used in the present invention are all known compounds and are produced according to known methods.
- the main physical properties of the refrigerant used in the present invention are as shown in Table 1 below.
- Refrigerant CF 0 CF 2 CH 2 CF 3 (marked below (a), molecular weight 200)
- Refrigerant CHF 2 CF (CHF 2 ) CF 3 (hereinafter referred to as refrigerant) ( molecular weight 200 2
- Ozone destruction coefficient 0 A stabilizer may be used in combination with the refrigerant of the present invention, if necessary. That is, when a high degree of stability is required under severe use conditions, epoxides such as propylene oxide, 1,2-butylene oxide, and glycidyl; dimethyl phosphite; Phosphites such as triisopropyl phosphite, diphenyl phosphite; triphosphorites such as trilaurine oletrito phosphite; tripheno Phosphine sulfides such as xyphosphin sulfide and trimethyl phosphine sulfide; boric acid, trinethyl bolate, trifluorophenyl borane, phenyl boronin New paper Boron compounds such as acid and diphenylboronic acid; 2,6-di-tert-butyl.
- epoxides such as propylene oxide, 1,2-
- Phenols such as lacresole; nitroalkanes such as nitromethane and nitroethane; acrylate esters such as methyl acrylate and ethyl acrylate; and other dioxane, tert.-butanol, and pen as possible out to the stabilizer such as adding approximately 0 0 1-5% of the refrigerant weight; Taerisuri Torr, Nono 0 Raisopuro Bae Nirutoruen..
- ethers such as dimethyl ether and pentafluoromethyl ether
- amines such as perfluoroethylamine
- LPG liquid phase polymer
- the refrigerant according to the present invention has a relatively excellent refrigerant performance because the compressor gas discharge temperature is low and the evaporating pressure and the condensing pressure are in appropriate ranges.
- the refrigerant (e) and the refrigerant (f) can be easily operated in a range higher than the heat cycle temperature range implemented in the present invention because the evaporating pressure and the condensing pressure are relatively low.
- the refrigerant (a) and the refrigerant (b) have a refrigerating capacity equal to or higher than that of the CFC 11 and exhibit an overall excellent performance that the coefficient of performance is about the same. Therefore, it can be replaced with CFC11 used as a refrigerant for turbochargers.
- 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 oil, polyester-based oil 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 5 ° C
- the condensing temperature is 40 ° C
- the superheat temperature at the compressor inlet is 12 ° C and the supercooling degree at the condenser outlet is 5 ° C. 0 Driving was performed.
- Polyalkylene glycol was used as refrigerating machine oil.
- Table 2 shows the coefficient of performance (COP), refrigeration capacity [kcalZm 3 ], and compressor gas discharge temperature (° C).
- Table 2 also shows the results of CFC 11 for comparison.
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)
Abstract
Réfrigérant comprenant un élément sélectionné dans le groupe formé des composés suivants: CF3CF2CH2CF3, CF3CH(CHF2)CF3, CF3CHFCF2CHF2, CF3CF2CF2CH2F, CHF2CF2CF2CHF2 et CHF2CF(CHF2)CF3. On décrit également un réfrigérateur contenant ce réfrigérant, ainsi que son utilisation.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3303386A JPH05140547A (ja) | 1991-11-19 | 1991-11-19 | オクタフルオロブタンからなる冷媒 |
JP3/303386 | 1991-11-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1993010203A1 true WO1993010203A1 (fr) | 1993-05-27 |
Family
ID=17920398
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1992/001502 WO1993010203A1 (fr) | 1991-11-19 | 1992-11-18 | Refrigerant comprenant de l'octafluorobutane |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPH05140547A (fr) |
WO (1) | WO1993010203A1 (fr) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996010061A1 (fr) * | 1994-09-29 | 1996-04-04 | E.I. Du Pont De Nemours And Company | Compositions a base d'octafluorobutane |
EP0735124A1 (fr) * | 1995-03-28 | 1996-10-02 | Elf Aquitaine | Composite actif à structure feuilletée et son utilisation comme milieu réactionnel |
US5562854A (en) * | 1994-09-29 | 1996-10-08 | E. I. Du Pont De Nemours And Company | Octafluorobutane compositions |
US5562853A (en) * | 1994-09-29 | 1996-10-08 | E. I. Du Pont De Nemours And Company | 1,1,2,2,3,3,4,4,-octafluorobutane compositions |
EP0738772A1 (fr) * | 1995-04-20 | 1996-10-23 | Elf Atochem S.A. | Mélanges pseudo-azéotropiques à base de difluorométhane et de pentafluorodiméthyléther, et leurs applications comme fluides frigorigènes |
US5626790A (en) * | 1992-11-19 | 1997-05-06 | E. I. Du Pont De Nemours And Company | Refrigerant compositions including 1,1,2-trifluoroethane and hexafluoropropane |
US5681800A (en) * | 1994-12-08 | 1997-10-28 | Exxon Chemical Patents Inc. | Biodegradable branched synthetic ester base stocks and lubricants formed therefrom |
US5688431A (en) * | 1994-09-29 | 1997-11-18 | E. I. Du Pont De Nemours And Company | Octafluorobutane compositions |
US5705471A (en) * | 1994-09-29 | 1998-01-06 | E. I. Du Pont De Nemours And Company | 1,1,2,2,3,3,4,4-octaflourobutane compositions |
US5730894A (en) * | 1996-04-16 | 1998-03-24 | E. I. Du Pont De Nemours And Company | 1,1,2,2,3,3,4,4-octafluorobutane azeotropic (like) compositions |
US6156224A (en) * | 1992-06-19 | 2000-12-05 | Matsushita Electric Industrial Co., Ltd. | Working fluid containing perfluorodimethylether |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01153786A (ja) * | 1987-12-11 | 1989-06-15 | Asahi Glass Co Ltd | 作動媒体混合物 |
EP0431458A1 (fr) * | 1989-12-07 | 1991-06-12 | Daikin Industries, Limited | Composition de nettoyage |
JPH03229732A (ja) * | 1990-02-02 | 1991-10-11 | Asahi Glass Co Ltd | スチレン系樹脂発泡体の製造方法 |
-
1991
- 1991-11-19 JP JP3303386A patent/JPH05140547A/ja active Pending
-
1992
- 1992-11-18 WO PCT/JP1992/001502 patent/WO1993010203A1/fr active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01153786A (ja) * | 1987-12-11 | 1989-06-15 | Asahi Glass Co Ltd | 作動媒体混合物 |
EP0431458A1 (fr) * | 1989-12-07 | 1991-06-12 | Daikin Industries, Limited | Composition de nettoyage |
JPH03229732A (ja) * | 1990-02-02 | 1991-10-11 | Asahi Glass Co Ltd | スチレン系樹脂発泡体の製造方法 |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6156224A (en) * | 1992-06-19 | 2000-12-05 | Matsushita Electric Industrial Co., Ltd. | Working fluid containing perfluorodimethylether |
US5626790A (en) * | 1992-11-19 | 1997-05-06 | E. I. Du Pont De Nemours And Company | Refrigerant compositions including 1,1,2-trifluoroethane and hexafluoropropane |
US5653908A (en) * | 1994-09-29 | 1997-08-05 | E. I. Du Pont De Nemours And Company | Octafluorobutane compositions |
US5705471A (en) * | 1994-09-29 | 1998-01-06 | E. I. Du Pont De Nemours And Company | 1,1,2,2,3,3,4,4-octaflourobutane compositions |
US5562853A (en) * | 1994-09-29 | 1996-10-08 | E. I. Du Pont De Nemours And Company | 1,1,2,2,3,3,4,4,-octafluorobutane compositions |
US5772911A (en) * | 1994-09-29 | 1998-06-30 | E. I. Du Pont De Nemours And Company | 1,1,2,2,3,3,4,4-Octafluorobutane compositions |
US5562855A (en) * | 1994-09-29 | 1996-10-08 | E. I. Du Pont De Nemours And Company | Octafluorobutane compositions |
US5562854A (en) * | 1994-09-29 | 1996-10-08 | E. I. Du Pont De Nemours And Company | Octafluorobutane compositions |
WO1996010061A1 (fr) * | 1994-09-29 | 1996-04-04 | E.I. Du Pont De Nemours And Company | Compositions a base d'octafluorobutane |
US5654264A (en) * | 1994-09-29 | 1997-08-05 | 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 |
US5681800A (en) * | 1994-12-08 | 1997-10-28 | Exxon Chemical Patents Inc. | Biodegradable branched synthetic ester base stocks and lubricants formed therefrom |
EP0735124A1 (fr) * | 1995-03-28 | 1996-10-02 | Elf Aquitaine | Composite actif à structure feuilletée et son utilisation comme milieu réactionnel |
FR2733241A1 (fr) * | 1995-04-20 | 1996-10-25 | Atochem Elf Sa | Melanges pseudo-azeotropiques a base de difluoromethane et de pentafluorodimethylether , et leurs applications comme fluides frigorigenes |
EP0738772A1 (fr) * | 1995-04-20 | 1996-10-23 | Elf Atochem S.A. | Mélanges pseudo-azéotropiques à base de difluorométhane et de pentafluorodiméthyléther, et leurs applications comme fluides frigorigènes |
US5730894A (en) * | 1996-04-16 | 1998-03-24 | E. I. Du Pont De Nemours And Company | 1,1,2,2,3,3,4,4-octafluorobutane azeotropic (like) compositions |
Also Published As
Publication number | Publication date |
---|---|
JPH05140547A (ja) | 1993-06-08 |
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