US20090056333A1 - Working Fluid For An Orc Process, Orc Process and Orc Apparatus - Google Patents
Working Fluid For An Orc Process, Orc Process and Orc Apparatus Download PDFInfo
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- US20090056333A1 US20090056333A1 US12/066,018 US6601806A US2009056333A1 US 20090056333 A1 US20090056333 A1 US 20090056333A1 US 6601806 A US6601806 A US 6601806A US 2009056333 A1 US2009056333 A1 US 2009056333A1
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- working fluid
- partially
- perfluorinated
- orc
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- 239000012530 fluid Substances 0.000 title claims abstract description 79
- 238000000034 method Methods 0.000 title claims abstract description 27
- WZLFPVPRZGTCKP-UHFFFAOYSA-N 1,1,1,3,3-pentafluorobutane Chemical compound CC(F)(F)CC(F)(F)F WZLFPVPRZGTCKP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 150000002576 ketones Chemical class 0.000 claims abstract description 18
- 229920000570 polyether Polymers 0.000 claims abstract description 16
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 13
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 13
- 238000009835 boiling Methods 0.000 claims abstract description 12
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 29
- 150000001875 compounds Chemical class 0.000 claims description 17
- MSSNHSVIGIHOJA-UHFFFAOYSA-N pentafluoropropane Chemical compound FC(F)CC(F)(F)F MSSNHSVIGIHOJA-UHFFFAOYSA-N 0.000 claims description 11
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims description 7
- RIQRGMUSBYGDBL-UHFFFAOYSA-N 1,1,1,2,2,3,4,5,5,5-decafluoropentane Chemical compound FC(F)(F)C(F)C(F)C(F)(F)C(F)(F)F RIQRGMUSBYGDBL-UHFFFAOYSA-N 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- -1 hepafluorobutane Chemical compound 0.000 claims description 5
- 229960004624 perflexane Drugs 0.000 claims description 5
- ZJIJAJXFLBMLCK-UHFFFAOYSA-N perfluorohexane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F ZJIJAJXFLBMLCK-UHFFFAOYSA-N 0.000 claims description 5
- BSRRYOGYBQJAFP-UHFFFAOYSA-N 1,1,1,2,2,3-hexafluorobutane Chemical compound CC(F)C(F)(F)C(F)(F)F BSRRYOGYBQJAFP-UHFFFAOYSA-N 0.000 claims description 4
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 claims description 4
- ABQIAHFCJGVSDJ-UHFFFAOYSA-N 1,1,1,3,4,4,4-heptafluoro-3-(trifluoromethyl)butan-2-one Chemical compound FC(F)(F)C(=O)C(F)(C(F)(F)F)C(F)(F)F ABQIAHFCJGVSDJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 229960004692 perflenapent Drugs 0.000 claims description 4
- NJCBUSHGCBERSK-UHFFFAOYSA-N perfluoropentane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F NJCBUSHGCBERSK-UHFFFAOYSA-N 0.000 claims description 4
- DUAKCVSNUIDZMC-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptafluorobutane Chemical compound CC(F)(F)C(F)(F)C(F)(F)F DUAKCVSNUIDZMC-UHFFFAOYSA-N 0.000 claims description 3
- NVSXSBBVEDNGPY-UHFFFAOYSA-N 1,1,1,2,2-pentafluorobutane Chemical compound CCC(F)(F)C(F)(F)F NVSXSBBVEDNGPY-UHFFFAOYSA-N 0.000 claims description 3
- 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 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- UKACHOXRXFQJFN-UHFFFAOYSA-N heptafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)F UKACHOXRXFQJFN-UHFFFAOYSA-N 0.000 claims description 3
- 125000006342 heptafluoro i-propyl group Chemical group FC(F)(F)C(F)(*)C(F)(F)F 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 8
- 239000010702 perfluoropolyether Substances 0.000 description 11
- 239000002918 waste heat Substances 0.000 description 7
- 239000002028 Biomass Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 101100269308 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) PFS1 gene Proteins 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 150000005828 hydrofluoroalkanes Chemical class 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000004449 solid propellant Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
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- 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
- 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
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01K—STEAM ENGINE PLANTS; STEAM ACCUMULATORS; ENGINE PLANTS NOT OTHERWISE PROVIDED FOR; ENGINES USING SPECIAL WORKING FLUIDS OR CYCLES
- F01K25/00—Plants or engines characterised by use of special working fluids, not otherwise provided for; Plants operating in closed cycles and not otherwise provided for
- F01K25/06—Plants or engines characterised by use of special working fluids, not otherwise provided for; Plants operating in closed cycles and not otherwise provided for using mixtures of different fluids
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01K—STEAM ENGINE PLANTS; STEAM ACCUMULATORS; ENGINE PLANTS NOT OTHERWISE PROVIDED FOR; ENGINES USING SPECIAL WORKING FLUIDS OR CYCLES
- F01K25/00—Plants or engines characterised by use of special working fluids, not otherwise provided for; Plants operating in closed cycles and not otherwise provided for
- F01K25/08—Plants or engines characterised by use of special working fluids, not otherwise provided for; Plants operating in closed cycles and not otherwise provided for using special vapours
Definitions
- the invention relates to working fluids for an ORC process for energy conversion in a thermal cycle process for combined generation of electrical and heat energy, to an ORC process and to an apparatus for performing an ORC process.
- the ORC (organic Rankine cycle) process is a thermodynamic cycle named after William Rankine.
- ORC installations convert thermal energy into electric current.
- selection of the appropriate working fluids allows temperature differences to be bridged and utilized.
- Such plants are utilized for the electrical energy generation from the waste heat of plants for glass production, cement furnaces, steel furnaces and other processes with waste heat of a temperature greater than 150° C.
- the utilization of geothermal heat, solar heat or the waste heat from the incineration of waste, biomass and other liquid or solid fuels, or combined operation of gas turbines and waste heat utilization, is likewise possible by means of an ORC process.
- Geothermal heat can either be utilized directly or be converted to electrical energy.
- the conversion of the geothermal heat to electrical energy is becoming ever more significant.
- steam-powered processes operated with an organic working fluid ORC working fluid
- Such a system with an organic working fluid is composed of the main components of evaporator, turbine, condenser and feed pump, and the accompanying control and regulation elements.
- the working fluid is selected such that its thermodynamic properties are adjusted to the heat source present. Preference is given to using working fluids which evaporate at comparatively low temperatures.
- the geothermal heat is utilized as a heat source in the form of hot thermal water with a temperature of, for example, approx. 180° C.
- Thermal water with a lower temperature is likewise utilizable as a heat source, in which case a working fluid with appropriately low evaporation temperature has to be selected.
- the working fluid is preheated by the heat source, then superheated and finally decompressed in a turbine and, as this is done, via a shaft, drives a generator for electricity generation. Subsequently, the working fluid is condensed and compressed again by means of the feed pump and recycled into the preheater.
- the working fluids are selected taking account of the heat content of the heat source.
- the working fluid should be non-toxic and not have any ozone-depleting potential. Moreover, it should as far as possible not be combustible and also have a still appropriately low pressure at high temperatures.
- the working fluid should have a high thermal and chemical stability. Since working fluids are used in closed circuits which typically consist of metallic components, the question of reactivity and of corrosion behaviour toward the metals used is likewise an important aspect in the selection of the working fluids.
- Suitable working fluids which have already been used include hydrocarbons such as pentane, or halogenated hydrocarbons such as trifluoromethane, tetrafluoromethane, pentafluoropropane (EP 0 066 439, U.S. Pat. No. 6,880,344).
- hydrocarbons such as pentane
- halogenated hydrocarbons such as trifluoromethane, tetrafluoromethane, pentafluoropropane (EP 0 066 439, U.S. Pat. No. 6,880,344).
- a significant disadvantage in the case of use of pure hydrocarbons is their explosiveness.
- Still another subject of the present invention is to provide an apparatus for performing an ORC process.
- the working fluid comprising at least one compound selected from the group of the partially or perfluorinated hydrocarbons such as tetrafluoroethane, especially 1,1,1,2-tetrafluoroethane, pentafluoropropane, especially 1,1,1,3,3-pentafluoropropane, hexafluoropropane, heptafluoropropane, especially 1,1,1,2,3,3,3-heptafluoropropane, pentafluorobutane, especially 1,1,1,3,3-pentafluorobutane, hexafluorobutane, heptafluorobutane, decafluoropentane, perfluoropentane, perfluorohexane or mixtures thereof, and/or at least one compound from the group of the partially or perfluorinated polyethers and/or of the partially or perfluorinated ketones; by a ORC
- a working fluid comprising at least one compound selected from the group of the partially or perfluorinated hydrocarbons such as tetrafluoroethane, especially 1,1,1,2-tetrafluoroethane, pentafluoropropane, especially 1,1,1,3,3-pentafluoropropane, hexafluoropropane, heptafluoropropane, especially 1,1,1,2,3,3,3-heptafluoropropane, pentafluorobutane, especially 1,1,1,3,3-pentafluorobutane, hexafluorobutane, heptafluorobutane, decafluoropentane, perfluoropentane, perfluorohexane or mixtures thereof, and/or at least one compound from the group of the partially or perfluorinated polyethers and/or of the partially or perfluorinated keto
- ORC working fluids are described in detail.
- the preferred embodiments of the ORC working fluids as described in detail below are also preferred embodiments of the ORC process in which they are applied, and of the apparatus in which they are comprised.
- the inventive working fluid is selected from the multitude of suitable compounds or mixtures of these compounds such that the boiling point of the working fluid used is below the temperature of the heat source, so that the evaporation of the working fluid is possible without any great technical complexity.
- the composition of the mixtures is preferably selected such that an azeotropic or virtually azeotropic mixture is formed.
- the working fluid used is stable within the temperature range of interest and has good thermodynamic properties.
- Suitable perfluorinated polyethers are described, for example, in WO 02/38718. These perfluorinated polyethers consist essentially of carbon, fluorine and oxygen atoms and comprise at least two, preferably three, C—O—C ether linkages, or a mixture of several compounds satisfying that definition. Often, the oxygen atoms in the perfluoropolyether are exclusively present within the C—O—C ether linkages.
- the perfluoropolyethers generally have a molecular weight of about 200 or more. Generally they have a molecular weight of less than about 1500. If the polyether is a mixture of several substances, the molecular weight is the weight-average molecular weight.
- the perfluoropolyether has a boiling point greater than or equal to 40° C. at 101.3 kPa.
- the perfluoropolyether generally has a boiling point less or equal to about 200° C. at 101.3 kPa.
- these perfluoropolyethers often are a mixture of individual substances.
- the kinematic viscosity of the perfluoropolyether is less than or equal to 1 cSt (Centistoke) at 25° C. Generally, the kinematic viscosity is at least 0.3 cSt at 25° C.
- the preferred perfluoro polyethers used are the products marketed by Solvay Solexis under the names GALDEN® and FOMBLIN®.
- Examples include:
- GALDEN® HT 55 boiling point 57° C. at 101.3 kPA; average molecular weight 340
- GALDEN® HT 70 boiling point 66° C. at 101.3 kPa; average molecular weight 410
- FOMBLIN® PFS1 boiling point 90° C. at 101.3 kPa; average molecular weight 460
- the suitable partially fluorinated polyethers used may be the hydrofluoro ethers marketed by 3M under the name NOVEC®.
- the GALDEN® and FOMBLIN® systems are usually multicomponent systems having a boiling point in the range from 40 to 76° C.
- the partially fluorinated hydrocarbons used are especially 1,1,1,3,3-pentafluorobutane (HFC-365mfc), 1,1,1,2-tetrafluoroethane (HFC 134a), 1,1,1,3,3-pentafluoropropane (HFC 245fa) or their mixtures with one another.
- HFC-365mfc 1,1,1,2-tetrafluoroethane
- HFC 134a 1,1,1,3,3-pentafluoropropane
- HFC 245fa 1,1,1,3,3-pentafluoropropane
- the partially or perfluorinated polyethers used are preferably GALDEN®HT 55, GALDEN® HT 70.
- the fluorinated ketones used are partially or perfluorinated ketones of the general formula R—C(O)—R′ where R and R′ are partially or perfluorinated substituents which may be the same or different and are preferably fluorinated alkyl groups. However, R may also be a linear or branched alkyl group.
- the fluorinated alkyl groups having preferably 1 to 6 carbon atoms may likewise be linear or branched, in which case not more than two fluorine atoms may be replaced by hydrogen.
- R is preferably perfluoroisopropyl and R′ is preferably a trifluoromethyl or pentafluoroethyl group.
- the partially fluorinated ketone used is a compound of the abovementioned general formula in which R is a linear or branched alkyl group, preferably a methyl group, and R′ is as defined above.
- R is a linear or branched alkyl group, preferably a methyl group
- R′ is as defined above.
- Mixtures of the ketones with the fluorinated hydrocarbons are likewise suitable. The preparation of these fluorinated ketones is described in EP 1 261 398.
- the boiling points of the suitable ketones are within the range from 0° C. to about 150° C., preferably in the range from 0° C. to about 110° C., in particular in the range from 0° C. to about 75° C.
- fluorinated ketones from the group of CF 3 C(O)CF(CF 3 ) 2 , CF 3 CF 2 C(O)CF(CF 3 ) 2 , CH 3 C(O)CF 2 CF 2 H, CH 3 C(O)CF 2 CFHCF 3 are used.
- the ketones are used as a working fluid in combination with partially or perfluorinated hydrocarbons.
- mixtures which comprise or consist of HFC-365mfc and at least one compound of the ketones mentioned, preferably CF 3 C(O)CF(CF 3 ) 2 are used.
- a preferred embodiment concerns mixtures comprising one or more hydrofluorocarbons and one or more (partially and/or per-)fluorinated ethers and/or one or more (partially and/or per-)fluorinated ketones.
- mixtures comprising 1,1,1,3,3-pentafluorobutane (HFC-365mfc) and/or 1,1,1,3,3-pentafluoropropane (HFC 245fa) as hydrofluorocarbons(s).
- compositions described in WO 02/38718 are especially suitable as working fluids according to the present invention.
- the weight ratio of the hydrofluoroalkane to the perfluoropolyether is generally greater than or equal to 5:95, often greater than or equal to 10:90, preferably greater than or equal to 25:75.
- the weight ratio of the hydrofluoroalkane to the perfluoropolyether is generally less than or equal to 95:5, often less than or equal to 90:10, preferably less than or equal to 85:15.
- the binary azeotropes or pseudo-azeotropes formed from HFC-365mfc and especially the perfluoropolyethers GALDEN® HT55, GALDEN® HT70 or FOMBLIN® PFS1, which are described in WO 02/38718, are examples for suitable mixtures useful as ORC working fluids according to the present invention.
- the working fluid used is a mixture of HFC-365mfc and GALDEN® HT 55 in a mixing ratio of 65 to 35%.
- HFC-365mfc and hydrofluoroethers or HFC-365mfc and perfluorohexane or HFC-365mfc and perfluoropentane or HFC-365mfc and decafluoropentane are likewise preferred working fluids, especially for energy conversion using geothermal water as the heat source.
- the mixing ratio may be different and, for example, be 50/50, 40/60 or 65/35.
- the mixing ratio should be selected such that an azeotropic or virtually azeotropic mixture is formed.
- the inventive working fluids may especially be used for energy conversion starting from heat sources having a temperature of about 50 to 180° C. They are particularly suitable for conversion of geothermal heat, in the form of thermal water, to electrical energy. Energy conversion utilizing other heat sources, such as solar heat or waste heat from refuse incineration, biomass or other liquid or solid fuels is likewise conceivable.
- Suitable biomass includes, for example, biomass from plants or feces from animal husbandry.
- waste heat e.g. from industrial processes
- the conversion is performed in an installation or plant for combined heat and power, e.g. in a communal heating/power station.
- the working fluids mentioned above are suitable for cooling photo-voltaic cells for increasing the conversion of solar energy.
- the heat energy absorbed thereby can be utilized for example, according to the present invention, for conversion into additional electric energy. Cooling can be effected here separately, e.g. via a flange-mounted structural element, but as well by direct immersion of the photo-voltaic cells into the working fluid (immersion cooling).
- the working fluids according to the present invention can be applied to use heat sources directly in work machines or processing machines, such as, for example, decentralized work or processing machines, especially autarchic pumps in which, for example, solar energy is converted into mechanical energy.
- decentralized means in this context especially that the work or processing machine is supplied essentially according to the present invention with energy from a heat source which naturally occurs at the location of the work or processing machine, or which was created artificially for the needs of the work or processing machine.
- Combination of a plurality of process stages, for example in the form of secondary cycles, allows the efficiency of the plants to be increased.
- the working fluids used in the individual secondary cycles may be the same or different.
- the waste heat of the individual secondary cycles of the cycle process is sent in each case to the next process or the next stage.
- the working fluids may be selected such that they have different vapour pressures as a function of the temperature, and the vapour pressures should each be within the optimal range.
- the thermal water is delivered into the plant with a depth pump.
- the heat is released to the working fluid in a preheater and an evaporator.
- the working fluid circulates in a so-called secondary circuit, where, after the pressure increase by the feed pump, it passes through the preheater and the evaporator.
- the superheated steam is decompressed in the turbine and drives, via a shaft, a generator for electricity generation. The decompression does not proceed above the condensation curve, but rather always remains outside the wet steam range.
- the decompressed fluid is thus still superheated and this heat must be removed before the working fluid condenses and it is passed back to the preheater.
- the removed heat can for example be used to heat rooms.
- the preferred working fluids especially a mixture of 60 to 70% by weight, preferably 65% by weight, of HFC-365mfc, and 30 to 40% by weight, preferably 35% by weight, GALDEN® HT55 perfluoropolyethers, are especially suitable for all of the applications described above.
- An apparatus comprising the ORC working fluid according to the present invention, suitable for performing the ORC process of the present invention is also subject of the present invention.
- Such apparatus in principle are known. They usually comprise means to heat up the ORC working fluid, e.g. an evaporator, optionally a preheater and/or superheater, a turbine which is connected to a generator for producing electrical current, and a heat consumer (condenser) for the ORC working fluid.
- FIG. 1 gives a sketch of an apparatus according to the invention. It comprises an evaporator E, a line 1 which is connected to the evaporator and a heat consumer HC tvia a pump P in which the ORC fluid is compressed.
- line 1 liquid ORC working fluid is transported from the heat consumer HC to the evaporator E.
- the evaporator E is connected through a line 2 with a turbine T.
- ORC working fluid is transported in vapour form to the turbine T.
- Turbine T is connected to a generator G which produces electrical energy.
- the turbine T is connected to the heat consumer HC via line 3 .
- the vapour leaving the turbine through line 3 is condensed in the heat consumer HC.
- Evaporator E can be heated by respective heat sources like geothermal water, biomass etc.
- the apparatus according to the invention comprises one of the above-mentioned ORC working fluids.
- the heat generated in the heat consumer HC can for example be used for heating rooms.
- the ORC process starts from an external heat supply via a preheater and an evaporator.
- the heat source used was geothermal water having a temperature of 100° C.
- the fluid, a mixture of HFC-365mfc and GALDEN® HT 55 (mixing ratio 65/35% by weight) evaporates in the evaporator.
- the fluid vapour passes to a turbine which drives a generator for electricity generation.
- the fluid was conducted into a condenser (heat consumer) and the fluid condensed here was recycled back into the preheater.
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Abstract
The invention relates to working fluids for energy conversion in a thermal ORC process for combined generation of electrical and heat energy. The heat source used is in particular thermal water. The working fluids used are partially or perfluorinated hydrocarbons and/or partially or perfluorinated polyethers and/or partially or perfluorinated ketones. In one embodiment of the invention, the working fluid used is a combination of 1,1,1,3,3-pentafluorobutane and a fluorinated polyether having a molecular weight of 340 and a boiling point of 57° C. at 101.3 kPa.
Description
- The invention relates to working fluids for an ORC process for energy conversion in a thermal cycle process for combined generation of electrical and heat energy, to an ORC process and to an apparatus for performing an ORC process.
- The ORC (organic Rankine cycle) process is a thermodynamic cycle named after William Rankine. ORC installations convert thermal energy into electric current. In a thermal ORC process, selection of the appropriate working fluids allows temperature differences to be bridged and utilized. Such plants are utilized for the electrical energy generation from the waste heat of plants for glass production, cement furnaces, steel furnaces and other processes with waste heat of a temperature greater than 150° C. The utilization of geothermal heat, solar heat or the waste heat from the incineration of waste, biomass and other liquid or solid fuels, or combined operation of gas turbines and waste heat utilization, is likewise possible by means of an ORC process.
- Geothermal heat can either be utilized directly or be converted to electrical energy. The conversion of the geothermal heat to electrical energy is becoming ever more significant. Typically, steam-powered processes operated with an organic working fluid (ORC working fluid) are used here. Such a system with an organic working fluid is composed of the main components of evaporator, turbine, condenser and feed pump, and the accompanying control and regulation elements. The working fluid is selected such that its thermodynamic properties are adjusted to the heat source present. Preference is given to using working fluids which evaporate at comparatively low temperatures.
- The geothermal heat is utilized as a heat source in the form of hot thermal water with a temperature of, for example, approx. 180° C. Thermal water with a lower temperature is likewise utilizable as a heat source, in which case a working fluid with appropriately low evaporation temperature has to be selected.
- The working fluid is preheated by the heat source, then superheated and finally decompressed in a turbine and, as this is done, via a shaft, drives a generator for electricity generation. Subsequently, the working fluid is condensed and compressed again by means of the feed pump and recycled into the preheater.
- In order to guarantee economically viable operation, particular requirements are made on the working fluid. In particular, the working fluids are selected taking account of the heat content of the heat source.
- The working fluid should be non-toxic and not have any ozone-depleting potential. Moreover, it should as far as possible not be combustible and also have a still appropriately low pressure at high temperatures. The working fluid should have a high thermal and chemical stability. Since working fluids are used in closed circuits which typically consist of metallic components, the question of reactivity and of corrosion behaviour toward the metals used is likewise an important aspect in the selection of the working fluids.
- To limit the capital costs for the turbines, the use of working fluids with high molecular weight has been found to be advantageous. Owing to their relatively low speed, the utilizable kinetic energy of heavy molecules can largely be dissipated with one turbine blade ring or only a few turbine blade rings at maximum turbine speed. In the case of lighter and hence more mobile fluids, in the acquisition, either more expensive larger turbines or two-stage turbines are required to achieve high rotational speeds, or additional gears have to be incorporated.
- Examples of suitable working fluids which have already been used include hydrocarbons such as pentane, or halogenated hydrocarbons such as trifluoromethane, tetrafluoromethane, pentafluoropropane (EP 0 066 439, U.S. Pat. No. 6,880,344). A significant disadvantage in the case of use of pure hydrocarbons is their explosiveness.
- It is an object of the invention to provide a working fluid for energy recovery, especially for utilization of heat sources having a temperature up to approx. 200° C., preferably up to approx. 180° C., which satisfies the requirements mentioned.
- It is another object of the invention to provide a method for energy recovery, especially for utilization of heat sources having a temperature up to approx. 200° C., preferably up to approx. 180° C., which satisfies the requirements mentioned.
- Still another subject of the present invention is to provide an apparatus for performing an ORC process.
- These and other objects of the present invention are achieved by virtue of the working fluid comprising at least one compound selected from the group of the partially or perfluorinated hydrocarbons such as tetrafluoroethane, especially 1,1,1,2-tetrafluoroethane, pentafluoropropane, especially 1,1,1,3,3-pentafluoropropane, hexafluoropropane, heptafluoropropane, especially 1,1,1,2,3,3,3-heptafluoropropane, pentafluorobutane, especially 1,1,1,3,3-pentafluorobutane, hexafluorobutane, heptafluorobutane, decafluoropentane, perfluoropentane, perfluorohexane or mixtures thereof, and/or at least one compound from the group of the partially or perfluorinated polyethers and/or of the partially or perfluorinated ketones; by a ORC process for energy recovery, preferably for utilization of heat sources having a temperature up to approx. 200° C., preferably up to approx. 180° C., in which a working fluid comprising at least one compound selected from the group of the partially or perfluorinated hydrocarbons such as tetrafluoroethane, especially 1,1,1,2-tetrafluoroethane, pentafluoropropane, especially 1,1,1,3,3-pentafluoropropane, hexafluoropropane, heptafluoropropane, especially 1,1,1,2,3,3,3-heptafluoropropane, pentafluorobutane, especially 1,1,1,3,3-pentafluorobutane, hexafluorobutane, heptafluorobutane, decafluoropentane, perfluoropentane, perfluorohexane or mixtures thereof, and/or at least one compound from the group of the partially or perfluorinated polyethers and/or of the partially or perfluorinated ketones is applied; and by the apparatus comprising the ORC working fluid according to the present invention.
- In the following, the ORC working fluids are described in detail. The preferred embodiments of the ORC working fluids as described in detail below are also preferred embodiments of the ORC process in which they are applied, and of the apparatus in which they are comprised.
- Mixtures of the fluorinated hydrocarbons mentioned above, with the fluorinated polyethers and/or ketones mentioned above may likewise be used as the working fluid for an ORC process and are preferred as working fluids according to the present invention. The inventive working fluid is selected from the multitude of suitable compounds or mixtures of these compounds such that the boiling point of the working fluid used is below the temperature of the heat source, so that the evaporation of the working fluid is possible without any great technical complexity. The composition of the mixtures is preferably selected such that an azeotropic or virtually azeotropic mixture is formed.
- The working fluid used is stable within the temperature range of interest and has good thermodynamic properties.
- Suitable perfluorinated polyethers are described, for example, in WO 02/38718. These perfluorinated polyethers consist essentially of carbon, fluorine and oxygen atoms and comprise at least two, preferably three, C—O—C ether linkages, or a mixture of several compounds satisfying that definition. Often, the oxygen atoms in the perfluoropolyether are exclusively present within the C—O—C ether linkages. The perfluoropolyethers generally have a molecular weight of about 200 or more. Generally they have a molecular weight of less than about 1500. If the polyether is a mixture of several substances, the molecular weight is the weight-average molecular weight. Generally, the perfluoropolyether has a boiling point greater than or equal to 40° C. at 101.3 kPa. The perfluoropolyether generally has a boiling point less or equal to about 200° C. at 101.3 kPa. As a result of the preparation, these perfluoropolyethers often are a mixture of individual substances.
- Generally, the kinematic viscosity of the perfluoropolyether is less than or equal to 1 cSt (Centistoke) at 25° C. Generally, the kinematic viscosity is at least 0.3 cSt at 25° C.
- The preferred perfluoro polyethers used are the products marketed by Solvay Solexis under the names GALDEN® and FOMBLIN®.
- Examples include:
- GALDEN® HT 55: boiling point 57° C. at 101.3 kPA; average molecular weight 340
- GALDEN® HT 70: boiling point 66° C. at 101.3 kPa; average molecular weight 410
- FOMBLIN® PFS1: boiling point 90° C. at 101.3 kPa; average molecular weight 460
- The suitable partially fluorinated polyethers used may be the hydrofluoro ethers marketed by 3M under the name NOVEC®. The GALDEN® and FOMBLIN® systems are usually multicomponent systems having a boiling point in the range from 40 to 76° C.
- In a preferred embodiment of the invention, the partially fluorinated hydrocarbons used are especially 1,1,1,3,3-pentafluorobutane (HFC-365mfc), 1,1,1,2-tetrafluoroethane (HFC 134a), 1,1,1,3,3-pentafluoropropane (HFC 245fa) or their mixtures with one another.
- The partially or perfluorinated polyethers used are preferably GALDEN®HT 55, GALDEN® HT 70.
- Mixtures of the polyethers with the fluorinated hydrocarbons are likewise suitable working fluids in the context of the invention.
- The fluorinated ketones used are partially or perfluorinated ketones of the general formula R—C(O)—R′ where R and R′ are partially or perfluorinated substituents which may be the same or different and are preferably fluorinated alkyl groups. However, R may also be a linear or branched alkyl group. The fluorinated alkyl groups having preferably 1 to 6 carbon atoms may likewise be linear or branched, in which case not more than two fluorine atoms may be replaced by hydrogen. R is preferably perfluoroisopropyl and R′ is preferably a trifluoromethyl or pentafluoroethyl group. In one embodiment, the partially fluorinated ketone used is a compound of the abovementioned general formula in which R is a linear or branched alkyl group, preferably a methyl group, and R′ is as defined above. Mixtures of the ketones with the fluorinated hydrocarbons are likewise suitable. The preparation of these fluorinated ketones is described in
EP 1 261 398. The boiling points of the suitable ketones are within the range from 0° C. to about 150° C., preferably in the range from 0° C. to about 110° C., in particular in the range from 0° C. to about 75° C. - In a preferred embodiment, fluorinated ketones from the group of CF3C(O)CF(CF3)2, CF3CF2C(O)CF(CF3)2, CH3C(O)CF2CF2H, CH3C(O)CF2CFHCF3 are used. In a further preferred embodiment, the ketones are used as a working fluid in combination with partially or perfluorinated hydrocarbons. In particular, mixtures which comprise or consist of HFC-365mfc and at least one compound of the ketones mentioned, preferably CF3C(O)CF(CF3)2, are used.
- A preferred embodiment concerns mixtures comprising one or more hydrofluorocarbons and one or more (partially and/or per-)fluorinated ethers and/or one or more (partially and/or per-)fluorinated ketones. Especially preferred are such mixtures comprising 1,1,1,3,3-pentafluorobutane (HFC-365mfc) and/or 1,1,1,3,3-pentafluoropropane (HFC 245fa) as hydrofluorocarbons(s).
- Compositions described in WO 02/38718 are especially suitable as working fluids according to the present invention.
- In the compositions described therein, the weight ratio of the hydrofluoroalkane to the perfluoropolyether is generally greater than or equal to 5:95, often greater than or equal to 10:90, preferably greater than or equal to 25:75. The weight ratio of the hydrofluoroalkane to the perfluoropolyether is generally less than or equal to 95:5, often less than or equal to 90:10, preferably less than or equal to 85:15.
- The binary azeotropes or pseudo-azeotropes formed from HFC-365mfc and especially the perfluoropolyethers GALDEN® HT55, GALDEN® HT70 or FOMBLIN® PFS1, which are described in WO 02/38718, are examples for suitable mixtures useful as ORC working fluids according to the present invention.
- In a further especially preferred embodiment, the working fluid used is a mixture of HFC-365mfc and GALDEN® HT 55 in a mixing ratio of 65 to 35%.
- Mixtures of HFC-365mfc and hydrofluoroethers or HFC-365mfc and perfluorohexane or HFC-365mfc and perfluoropentane or HFC-365mfc and decafluoropentane are likewise preferred working fluids, especially for energy conversion using geothermal water as the heat source. The mixing ratio may be different and, for example, be 50/50, 40/60 or 65/35. Advantageously, the mixing ratio should be selected such that an azeotropic or virtually azeotropic mixture is formed.
- The inventive working fluids may especially be used for energy conversion starting from heat sources having a temperature of about 50 to 180° C. They are particularly suitable for conversion of geothermal heat, in the form of thermal water, to electrical energy. Energy conversion utilizing other heat sources, such as solar heat or waste heat from refuse incineration, biomass or other liquid or solid fuels is likewise conceivable. Suitable biomass includes, for example, biomass from plants or feces from animal husbandry.
- Likewise, it is possible to convert waste heat, e.g. from industrial processes, according to the present invention. In another embodiment of the present invention, the conversion is performed in an installation or plant for combined heat and power, e.g. in a communal heating/power station.
- The working fluids mentioned above are suitable for cooling photo-voltaic cells for increasing the conversion of solar energy. The heat energy absorbed thereby can be utilized for example, according to the present invention, for conversion into additional electric energy. Cooling can be effected here separately, e.g. via a flange-mounted structural element, but as well by direct immersion of the photo-voltaic cells into the working fluid (immersion cooling).
- Further, the working fluids according to the present invention can be applied to use heat sources directly in work machines or processing machines, such as, for example, decentralized work or processing machines, especially autarchic pumps in which, for example, solar energy is converted into mechanical energy. The term “decentralized” means in this context especially that the work or processing machine is supplied essentially according to the present invention with energy from a heat source which naturally occurs at the location of the work or processing machine, or which was created artificially for the needs of the work or processing machine.
- Combination of a plurality of process stages, for example in the form of secondary cycles, allows the efficiency of the plants to be increased. The working fluids used in the individual secondary cycles may be the same or different. In this case, the waste heat of the individual secondary cycles of the cycle process is sent in each case to the next process or the next stage. In the case of use of different working fluids, the working fluids may be selected such that they have different vapour pressures as a function of the temperature, and the vapour pressures should each be within the optimal range. As a result of such a series connection of secondary circuits, the possibility exists of deriving heat energy, for example for heating purposes, after each stage.
- In one embodiment, the thermal water is delivered into the plant with a depth pump. Here, the heat is released to the working fluid in a preheater and an evaporator. The working fluid circulates in a so-called secondary circuit, where, after the pressure increase by the feed pump, it passes through the preheater and the evaporator. The superheated steam is decompressed in the turbine and drives, via a shaft, a generator for electricity generation. The decompression does not proceed above the condensation curve, but rather always remains outside the wet steam range. The decompressed fluid is thus still superheated and this heat must be removed before the working fluid condenses and it is passed back to the preheater. The removed heat can for example be used to heat rooms.
- The preferred working fluids, especially a mixture of 60 to 70% by weight, preferably 65% by weight, of HFC-365mfc, and 30 to 40% by weight, preferably 35% by weight, GALDEN® HT55 perfluoropolyethers, are especially suitable for all of the applications described above.
- An apparatus, comprising the ORC working fluid according to the present invention, suitable for performing the ORC process of the present invention is also subject of the present invention. Such apparatus in principle are known. They usually comprise means to heat up the ORC working fluid, e.g. an evaporator, optionally a preheater and/or superheater, a turbine which is connected to a generator for producing electrical current, and a heat consumer (condenser) for the ORC working fluid.
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FIG. 1 gives a sketch of an apparatus according to the invention. It comprises an evaporator E, aline 1 which is connected to the evaporator and a heat consumer HC tvia a pump P in which the ORC fluid is compressed. Throughline 1, liquid ORC working fluid is transported from the heat consumer HC to the evaporator E. The evaporator E is connected through aline 2 with a turbine T. Throughline 2, ORC working fluid is transported in vapour form to the turbine T. Turbine T is connected to a generator G which produces electrical energy. The turbine T is connected to the heat consumer HC vialine 3. The vapour leaving the turbine throughline 3 is condensed in the heat consumer HC. Evaporator E can be heated by respective heat sources like geothermal water, biomass etc. The apparatus according to the invention comprises one of the above-mentioned ORC working fluids. The heat generated in the heat consumer HC can for example be used for heating rooms. - The invention will be illustrated below using a working example.
- The ORC process starts from an external heat supply via a preheater and an evaporator.
- The heat source used was geothermal water having a temperature of 100° C. The fluid, a mixture of HFC-365mfc and GALDEN® HT 55 (mixing ratio 65/35% by weight) evaporates in the evaporator. The fluid vapour passes to a turbine which drives a generator for electricity generation. On the output side, the fluid was conducted into a condenser (heat consumer) and the fluid condensed here was recycled back into the preheater.
Claims (14)
1. A working fluid for an ORC process, comprising or consisting of at least one compound selected from the group of the partially or perfluorinated hydrocarbons and/or at least one compound from the group of the partially or perfluorinated polyethers and/or at least one compound from the group of the partially or perfluorinated ketones or a mixture of these compounds with one another.
2. A working fluid for an ORC process according to claim 1 , wherein the partially or perfluorinated hydrocarbon is at least one compound from the group of tetrafluoroethane, pentafluoropropane, hexafluoropropane, heptafluoropropane, pentafluorobutane, hexafluorobutane, heptafluorobutane, decafluoropentane, perfluoropentane, perfluorohexane or mixtures thereof.
3. A working fluid according to claim 2 further comprising at least one partially or perfluorinated polyethers.
4. A working fluid according to claim 1 , wherein the partially or perfluorinated polyethers have a boiling point greater than or equal to 40° C. at 101.3 kPa.
5. A working fluid according to claim 1 , wherein the partially or perfluorinated ethers have a boiling point equal to or less than about 200° C. at 101.3 kPa.
6. A working fluid according to claim 1 , comprising or consisting of a mixture of 1,1,1,3,3-pentafluorobutane and at least one perfluorinated polyether.
7. A working fluid according to claim 1 , wherein the at least one perfluorinated polyether has a boiling point of about 57° C. at 101.3 kPa.
8. A working fluid according to claim 1 , wherein the partially or perfluorinated ketones are selected from compounds having the general formula R—C(O) —R′, where R is an alkyl group, or a linear or branched fluorinated C1-C6-alkyl group in which not more than two fluorine atoms may be replaced by hydrogen, and R′ is a linear or branched fluorinated C1-C6 alkyl group in which not more than two fluorine atoms may be replaced by hydrogen.
9. A working fluid according to claim 1 , wherein the fluorinated ketones are selected from the group consisting of CF3C(O)CF(CF3)2, CF3CF2C(O)CF(CF3)2, CH3C(O)CF2CF2H, CH3C(O)CF2CFHCF3.
10. A working fluid according to claim 9 , comprising or consisting of a mixture of 1,1,1,3,3-pentafluorobutane and CF3C(O)CF(CF3)2.
11. An ORC process for converting heat into electrical energy wherein an ORC working fluid according to claim 10 is used as ORC working fluid.
12. An apparatus for performing an ORC process comprising an ORC working fluid according to claim 1 .
13. The working fluid for an ORC process according to claim 2 , wherein the partially or perfluorinated hydrocarbon is at least one compound from the group of 1,1,1,2-tetrafluoroethane, 1,1,1,3,3-pentafluoropropane, hexafluoropropane, 1,1,1,2,3,3,3-heptafluoropropane, 1,1,1,3,3-pentafluorobutane, hexafluorobutane, hepafluorobutane, decafluoropentane, perfluorohexane or mixtures thereof.
14. The working fluid according to claim 8 , wherein the partially or perfluorinated ketones are selected from compounds having the general formula R—C(O)—R′, where R is a methyl group, and R′ is a linear or branched fluorinated C1-C6 alkyl group in which not more than two fluorine atoms may be replaced by hydrogen.
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WO2011029488A1 (en) * | 2009-09-11 | 2011-03-17 | Abb Research Ltd | Transformer comprising a heat pipe |
CN102696081A (en) * | 2009-09-11 | 2012-09-26 | Abb研究有限公司 | Transformer comprising a heat pipe |
US8570131B2 (en) | 2009-10-19 | 2013-10-29 | Abb Technology Ag | Transformer |
US20120017591A1 (en) * | 2010-01-19 | 2012-01-26 | Leveson Philip D | Simultaneous production of electrical power and potable water |
ITMI20101121A1 (en) * | 2010-06-21 | 2011-12-22 | Exergy Engineering S R L | APPARATUS FOR CONVERTING THERMAL ENERGY IN ELECTRIC AND / OR MECHANICAL ENERGY THROUGH A RANKINE ORGANIC CYCLE |
US8820080B2 (en) * | 2010-06-28 | 2014-09-02 | Marvin Duane Julian | Nonfractionalized biomass-fueled refrigerant-based cogeneration |
DE102013205266A1 (en) * | 2013-03-26 | 2014-10-02 | Siemens Aktiengesellschaft | Heat engine and method for operating a heat engine |
US20170241679A1 (en) * | 2014-09-02 | 2017-08-24 | Cyclect Electrical Engineering Pte Ltd | Heat recovery system and method |
US10787936B2 (en) * | 2015-08-13 | 2020-09-29 | Gas Expansion Motors Limited | Thermodynamic engine |
Also Published As
Publication number | Publication date |
---|---|
RU2008115437A (en) | 2009-10-27 |
EP1929129A1 (en) | 2008-06-11 |
JP2009508978A (en) | 2009-03-05 |
WO2007033958A1 (en) | 2007-03-29 |
US8245512B2 (en) | 2012-08-21 |
CN101283162A (en) | 2008-10-08 |
ZA200802273B (en) | 2010-05-26 |
KR20080045716A (en) | 2008-05-23 |
US20110162366A1 (en) | 2011-07-07 |
EP1764487A1 (en) | 2007-03-21 |
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