US20200200483A1 - Removal of non-condensable gases from a closed loop process - Google Patents
Removal of non-condensable gases from a closed loop process Download PDFInfo
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- US20200200483A1 US20200200483A1 US16/595,199 US201916595199A US2020200483A1 US 20200200483 A1 US20200200483 A1 US 20200200483A1 US 201916595199 A US201916595199 A US 201916595199A US 2020200483 A1 US2020200483 A1 US 2020200483A1
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- condensation vessel
- valve
- working medium
- removal unit
- gas removal
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- 239000007789 gas Substances 0.000 title claims abstract description 95
- 238000000034 method Methods 0.000 title claims abstract description 53
- 238000009833 condensation Methods 0.000 claims description 62
- 230000005494 condensation Effects 0.000 claims description 62
- 239000012528 membrane Substances 0.000 claims description 13
- 238000001816 cooling Methods 0.000 claims description 5
- 239000007921 spray Substances 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 2
- 239000012530 fluid Substances 0.000 abstract description 32
- 150000001412 amines Chemical class 0.000 abstract description 19
- 238000010521 absorption reaction Methods 0.000 abstract description 18
- 239000007788 liquid Substances 0.000 abstract description 18
- 238000010248 power generation Methods 0.000 abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 8
- 230000006835 compression Effects 0.000 abstract description 5
- 238000007906 compression Methods 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052799 carbon Inorganic materials 0.000 abstract description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 32
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 17
- 239000001569 carbon dioxide Substances 0.000 description 16
- 229910002092 carbon dioxide Inorganic materials 0.000 description 16
- 239000000243 solution Substances 0.000 description 10
- 239000002904 solvent Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000006096 absorbing agent Substances 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- 238000005057 refrigeration Methods 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- -1 MEA Chemical class 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Images
Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F28—HEAT EXCHANGE IN GENERAL
- F28D—HEAT-EXCHANGE APPARATUS, NOT PROVIDED FOR IN ANOTHER SUBCLASS, IN WHICH THE HEAT-EXCHANGE MEDIA DO NOT COME INTO DIRECT CONTACT
- F28D15/00—Heat-exchange apparatus with the intermediate heat-transfer medium in closed tubes passing into or through the conduit walls ; Heat-exchange apparatus employing intermediate heat-transfer medium or bodies
- F28D15/02—Heat-exchange apparatus with the intermediate heat-transfer medium in closed tubes passing into or through the conduit walls ; Heat-exchange apparatus employing intermediate heat-transfer medium or bodies in which the medium condenses and evaporates, e.g. heat pipes
- F28D15/0258—Heat-exchange apparatus with the intermediate heat-transfer medium in closed tubes passing into or through the conduit walls ; Heat-exchange apparatus employing intermediate heat-transfer medium or bodies in which the medium condenses and evaporates, e.g. heat pipes with means to remove contaminants, e.g. getters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D5/00—Condensation of vapours; Recovering volatile solvents by condensation
- B01D5/0027—Condensation of vapours; Recovering volatile solvents by condensation by direct contact between vapours or gases and the cooling medium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D5/00—Condensation of vapours; Recovering volatile solvents by condensation
- B01D5/0033—Other features
- B01D5/0051—Regulation processes; Control systems, e.g. valves
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D5/00—Condensation of vapours; Recovering volatile solvents by condensation
- B01D5/0057—Condensation of vapours; Recovering volatile solvents by condensation in combination with other processes
- B01D5/0072—Condensation of vapours; Recovering volatile solvents by condensation in combination with other processes with filtration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D5/00—Condensation of vapours; Recovering volatile solvents by condensation
- B01D5/0078—Condensation of vapours; Recovering volatile solvents by condensation characterised by auxiliary systems or arrangements
- B01D5/0093—Removing and treatment of non condensable gases
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F28—HEAT EXCHANGE IN GENERAL
- F28F—DETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
- F28F23/00—Features relating to the use of intermediate heat-exchange materials, e.g. selection of compositions
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F28—HEAT EXCHANGE IN GENERAL
- F28F—DETAILS OF HEAT-EXCHANGE AND HEAT-TRANSFER APPARATUS, OF GENERAL APPLICATION
- F28F27/00—Control arrangements or safety devices specially adapted for heat-exchange or heat-transfer apparatus
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
-
- 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
- F01K13/00—General layout or general methods of operation of complete plants
- F01K13/02—Controlling, e.g. stopping or starting
-
- 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
- F01K7/00—Steam engine plants characterised by the use of specific types of engine; Plants or engines characterised by their use of special steam systems, cycles or processes; Control means specially adapted for such systems, cycles or processes; Use of withdrawn or exhaust steam for feed-water heating
- F01K7/16—Steam engine plants characterised by the use of specific types of engine; Plants or engines characterised by their use of special steam systems, cycles or processes; Control means specially adapted for such systems, cycles or processes; Use of withdrawn or exhaust steam for feed-water heating the engines being only of turbine type
Definitions
- This invention relates to removal of non-condensable gases from closed loop processes especially in the field of power generation.
- Non-condensable gas air including oxygen, nitrogen and argon, carbon dioxide (CO2); closed-loop power generation process: Rankine cycle, Organic Rankine cycle, ORC, Carbon Carrier
- tray- or spray-based deaerators are used to remove air, see “deaerator” e.g. in Wikipedia.
- Gas removal from water is affected by making use of Henry's law, i.e. reduced gas solubility at low partial pressure, and the principle that gas solubility is reduced at higher temperatures (see e.g. www.sterlingdearator.com).
- chemicals such as sodium sulphite can be employed as oxygen scavengers.
- U.S. Pat. No. 2,002,000 7732 discloses membrane based separation of a working fluid in power generation from non-condensable gas.
- WO 95/27 985 discusses various solutions attempted in the boiling water reactor industry, see pp. 10 chapter c.
- the C3 process as disclosed in WO 2012/128 715 comprises a CO2 gas loop driving a turbine whereby the CO2 gas is absorbed temporarily in the cold section of the process by e.g. amines and released from said amines at higher temperatures.
- the process results in a thermodynamic cycle operated between e.g. 2-3 bar on the high pressure side and 0.1-0.3 bar on the low pressure side, giving a high pressure quote and a high heat-to-electricity efficiency.
- air ingress on the vacuum side reduces the pressure quote. Therefore, air or other non-condensable gases have to be removed from the process.
- volatile amines shall not be ejected from the process.
- a vessel in which e.g. CO2 working fluid is absorbed is separated by valves from a power generation process, in particular C3 as described in WO 2012/128 715 and SE 2013/051 059, SE 1300 576-4, SE 1400 027-7 and SE 1400 160-6, hereby incorporated by reference, but also standard ORC solutions based on one or more volatile working fluids such as lower paraffins, classic refrigerants and in general ORC working fluids with boiling points at atmospheric pressure below 100.degree. C.
- said vessel may function as absorption chamber where CO2 gas is absorbed by amines.
- non-condensable gas comprising CO2, non-condensable gas, water and alkaline materials including amines may be compressed by raising the liquid level in said vessel.
- the concurrent pressure increase leads to the selective absorption of CO2 by alkaline materials. In this way, the concentration of volatile amines in the gas space is reduced.
- non-condensable gas may be vented, optionally through a filter or a membrane in order to absorb remaining volatile amine.
- a membrane or diaphragm may be used separating said vessel into two sections. Said membrane is permeable for air, but impermeable for volatile amines. Ideally, the membrane is not very permeable for CO2 gas.
- the membrane is ideally not in contact with liquid amine. Remaining or condensing liquid amine may be transferred back to the vessel, also without using a pump.
- the method is simple and economic as vacuum pumps may be omitted. However, using a vacuum pump is also considered an option for faster removal of non-condensable gases.
- FIG. 1 is a schematic drawing of an arrangement highly suitable for the removal of at least one gas from a closed loop process involving one or two working fluids which are condensed rather than chemically absorbed, further showing how the gas removal unit is integrated into the complete power generation process.
- This invention concerns in one aspect a method or procedure for the removal of at least one non-condensable gas from thermodynamic cycles, particularly from the C3 process mentioned above, which operates partly under vacuum, or ORC processes operating partly under vacuum.
- the working fluid may comprise a low boiling solvent such as methanol, ethanol, acetone, isopropanol or butanol on the one hand at a concentration of at least 5% by weight, and ammonia as well as amines including diethylamine, dipropylamine, dibutylamine, and water-soluble amines including MEA, in water or organic solvents, such as disclosed in above mentioned documents and CO2.
- a low boiling solvent such as methanol, ethanol, acetone, isopropanol or butanol on the one hand at a concentration of at least 5% by weight
- ammonia as well as amines including diethylamine, dipropylamine, dibutylamine, and water-soluble amines including MEA
- water or organic solvents such as disclosed in above mentioned documents and CO2.
- an absorption or condensation vessel 7 is in connection with a main absorbing or condensing vessel 50 through a valve 2 and a valve 4 .
- Air removal is achieved in batch operation using the following sequence:
- a valve 3 is opened to equilibrate the pressure in the condensation vessel 7 and the main condensing vessel 50 , while valves 2 , 4 and 5 are closed. Condensed working fluid is drained through a line 19 into the main condensing vessel 50 , prior to a pump 51 .
- a pump 24 is employed for working fluid transfer, e.g. if vessel 7 cannot be emptied by gravity.
- valve 4 is opened to start the spraying of cold condensed working fluid supplied through a line 16 .
- the valve 2 is opened to allow ingress of gas through a line 18 from the main condensing vessel 50 which in turn receives gas from turbine 53 .
- Pressures and temperatures are measured by sensors T 8 and T 9 and T 10 as well as P 12 and P 14 .
- T 8 ⁇ T 9 is approaching lower values ( ⁇ 30% of T 8 ⁇ T 10 )
- this may be taken as practical indication that no more gaseous working fluid is condensed in the condensation vessel 7 .
- the valves 2 and 3 are closed whereas the valve 4 remains open such that working fluid supply through the supply line 16 continues.
- Part of the remaining gaseous working fluid is condensed due to continued liquid flow and compression of the gas space which is now isolated, and the liquid level in the condensation vessel 7 rises.
- a further pump 13 may be provided for manipulating the absorption liquid level in said at least one absorption or condensation chamber 7 .
- valve 4 is closed as soon as the pressure P 12 in the condensation vessel 7 is close to or equal to the liquid pressure P 11 in the supply line 16 from a cooler 54 .
- valve 5 is opened such that a pump 20 can supply liquid to the condensation vessel 7 .
- the concurrent pressure increase leads to further condensation of gaseous working fluid.
- valve 1 As the pressure in the condensation vessel 7 is approaching the pressure P 14 in a supply line 17 which in turn is fed from the supply line 16 , the valve 1 is opened to release non-condensable gas through optional secondary vessel 22 , optional valve 21 and vent line 23 .
- Vessel 22 may serve as collection or recovery vessel for solvent if required. It is intended to eject as much air as possible, therefore, as a technical option, liquid supply through supply line 17 and valve 5 can continue until the liquid level in the condensation vessel 7 reaches a specified level. Ejection of liquid can be prevented by known methods, e.g. a floating device (not shown in FIG. 1 ) which blocks the valve 1 if the liquid level is at the maximum level. Diaphragms or membranes essentially impermeable to gases other than oxygen, nitrogen and argon are used e.g. in said secondary vessel 22 to avoid the loss of process gas, notably CO2 and volatile solvent and amine.
- the pressure in said at least one absorption or condensation chamber is at least 10%, preferably at least 30%, more preferably at least 80%, and most preferably even 150% higher than the pressure in a main absorption or condensation vessel ( 50 ).
- the driving force enabling gas separation and subsequent ejection from the closed loop process is the temperature difference between (one or more) condensation vessel(s) 7 and the main absorption or condensation vessel(s) 50 .
- This temperature difference is caused by the fact that liquid working fluid is pumped into the condensation vessel 7 at a higher rate, relative to the flow rate of gaseous working fluid, than into the main absorption vessel 50 . Therefore the liquid in the condensation vessel 7 is generally colder than in the main absorption vessel 50 .
- Gaseous working fluid and non-condensable gas is entering the condensation vessel 7 .
- the condensation of main working fluid leads to the enrichment of non-condensable gas in a gas space 6 which further causes the temperature to drop in the condensation vessel 7 .
- start sequence (C) described above it is practical to start sequence (C) described above.
- the fact that liquid in the condensation vessel 7 is colder than at any other stage in the process, is driving the gas separation. Cooling may be affected by the higher liquid flow rate, or alternatively by active cooling.
- the former method is using less energy, the latter method may be chosen in embodiments where e.g. space requirements dictate so.
- the complete closed-loop process is shown, here as a simple Rankine process with a heat exchanger 52 for generation of hot gaseous working fluid, a turbine 53 , the main condensation vessel 50 , the temperature sensor T 10 and a working medium pump 51 .
- working fluid exiting from heat exchanger/absorber/condenser 50 i.e. the main absorption vessel 50 can be partly recycled to the top of the same, e.g. to achieve a lower average temperature in said main absorption vessel 50 or to aid absorption in the main absorption vessel 50 .
- acetone is used as working fluid.
- the solubilities of resp. oxygen and nitrogen are very low in acetone (see Battino, J. Phys. Chem. Ref. Data Vol 12, No. 2, 1983, p. 174 and Vol. 13, No. 2, p. 587) such that air removal from acetone even at low temperature (e.g. between 20-40.degree. C. is efficient. Compared to prior-art solutions, loss of acetone or working fluid is significantly reduced.
- the gas mixture ejected from the process comprising non-condensable gas(es) and minor amounts of solvents including acetone, isopropanol, amines or the like is prevented from entering the environment by use of a cold trap, suitable filters such as carbon black, zeolites or other absorbents, a scrubber or a burning/flaring unit.
- removal of non-condensable gases may be automatically controlled e.g. by a software, whereby gas removal is triggered by one or more process sensor (T 8 , T 9 , T 10 and P 11 , P 12 and P 14 ) indicating ingress or presence of non-condensable gas, specifically using temperature and pressure sensors (T 8 , T 9 , T 10 and P 11 , P 12 and P 14 ), directly or indirectly indicating presence of non-condensable gas.
- process sensor T 8 , T 9 , T 10 and P 11 , P 12 and P 14
- the method described is also useful for air removal from a) steam-based Rankine cycles partly under vacuum but also from b) high pressure ORC systems.
- the method would be used to save costs, e.g. for a vacuum pump, in case b) this is relevant because already low air concentrations deteriorate the performance of heat exchangers such as condensers for ORC working fluids. Air ingress cannot be excluded despite the use of higher than atmospheric pressures.
- the technique for gas removal described above is used in a heat pump system.
- a separate gas compression step is used to generate higher temperatures, e.g. for house heating purposes, from low value heat sources.
- Suitable heat pump designs operating partly under vacuum are disclosed in SE 1300576-4 assigned to Climeon AB and related disclosures.
- diaphragms or membranes may be included to further reduce the loss of volatile materials such as amines, however, such solutions will be used depending on costs/benefits calculations.
- the methods disclosed here can be used in combination with closed-loop processes comprising working gas and chemicals as temporary and reversible working gas absorption agents.
- the methods can be used combination with the C3 thermodynamic cycle comprising CO2 as working gas and amines as temporary and reversible CO2 absorption agents.
- a thermodynamic cycle comprising paraffins such as propane, butane, pentane, hexane, and its isomers, alcohols such as methanol, ethanol, isopropanol, butanol or ketones such as acetone or refrigerants e.g. containing fluorine atoms or water as working gas at a concentration of at least 10% by weight.
- the methods can be used in combination with a heat pump or refrigeration system, preferably operating partly under vacuum.
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- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
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Abstract
A method which allows the ejection of non-condensable gases, notably air, from a closed loop power generation process or heat pump system, is disclosed. A vessel in which a working fluid is absorbed or condensed can be separated from the power generation processes by valves. Residual gas comprising CO2, non-condensable gas such as air, water and alkaline materials including amines may be compressed by raising the liquid level in said vessel. The concurrent pressure increase leads to the selective absorption of CO2 by alkaline materials. In simpler embodiments, mainly air is removed from one- or two-component processes. Following the compression, non-condensable gas may be vented, optionally through a filter. The method is simple and economic as vacuum pumps may be omitted. The method is useful for any power generation and Rankine cycle, and particularly useful for the power generation process known as C3 or Carbon Carrier Cycle.
Description
- This application is a divisional of U.S. patent application Ser. No. 15/301,350 entitled “REMOVAL OF NON-CONDENSABLE GASES FROM A CLOSED LOOP PROCESS” filed Sep. 30, 2016, (Attorney Docket No. CLIM 1003-3), which is a 371 application of and claims priority to PCT Application No: PCT/SE2015/050368 entitled “REMOVAL OF NON-CONDENSABLE GASES FROM A CLOSED LOOP PROCESS” filed Mar. 26, 2015, which claims priority to Swedish Application No: 1400349-5 filed Jul. 9, 2014 and Swedish Application No: 1400182-0 filed Apr. 4, 2014. The above applications are hereby incorporated by reference for all purposes.
- This invention relates to removal of non-condensable gases from closed loop processes especially in the field of power generation.
- Non-condensable gas: air including oxygen, nitrogen and argon, carbon dioxide (CO2); closed-loop power generation process: Rankine cycle, Organic Rankine cycle, ORC, Carbon Carrier
- Cycle, heat pump system involving compression/heating and expansion/cooling of a working fluid; vacuum: system pressure below 1 bar. In the text, a term such as CO2 or air may denote any non-condensable gas or mixture thereof.
- Accumulation of undesired gases is a known problem in fields such as chemical engineering and power plant operation. Gas, notably air, leaks into equipment not only operated under vacuum but even into processes operated above atmospheric pressure.
- In water-steam based power plants, tray- or spray-based deaerators are used to remove air, see “deaerator” e.g. in Wikipedia. Gas removal from water is affected by making use of Henry's law, i.e. reduced gas solubility at low partial pressure, and the principle that gas solubility is reduced at higher temperatures (see e.g. www.sterlingdearator.com). Also, chemicals such as sodium sulphite can be employed as oxygen scavengers.
- Numerous disclosures describe solutions of associated problems, including EP 1 829 594 (Asahi, 2004) for chemical processes, U.S. Pat. No. 4,026,111 (DOW, 1976) for removal of gas from brine for geothermal energy generation, U.S. Pat. No. 4,905,474 (steam condenser application), U.S. Pat. No. 7,588,631 (2006, vacuum deaeration by cyclones), and JP 2006 125 775 (Sanyo Electric, inventor Omori Mitsunori et al) which describes a vacuum pump solution ejecting non-condensable gases from a water/LiBr/octanol based refrigeration machine.
- U.S. Pat. No. 2,002,000 7732 discloses membrane based separation of a working fluid in power generation from non-condensable gas.
- WO 95/27 985 (Pennsylvania Power&Light Company) discusses various solutions attempted in the boiling water reactor industry, see pp. 10 chapter c.
- Relevant for this invention is U.S. Pat. No. 5,487,765 (Ormat, 1994) which discloses a separate vessel comprising a membrane or diaphragm through which non-condensable gases diffuse but which retains working fluids such as lower paraffins. This solution is highly useful in an ORC process (Organic Rankine Cycle) in which a working fluid such as butane or pentane (or HCFC) is evaporated at high temperatures and condensed at lower temperature. The pressure difference between the high and low temperature sections is used to operate a turbine for electricity generation.
- In energy-generation processes operated partly under vacuum, the risk of air ingress is obviously higher. The C3 process as disclosed in WO 2012/128 715 comprises a CO2 gas loop driving a turbine whereby the CO2 gas is absorbed temporarily in the cold section of the process by e.g. amines and released from said amines at higher temperatures. The process results in a thermodynamic cycle operated between e.g. 2-3 bar on the high pressure side and 0.1-0.3 bar on the low pressure side, giving a high pressure quote and a high heat-to-electricity efficiency. In this process, air ingress on the vacuum side reduces the pressure quote. Therefore, air or other non-condensable gases have to be removed from the process. At the same time, volatile amines shall not be ejected from the process.
- Further to the problems not solved by prior art, pumping out residual gas, whether directly from the absorber or condenser or from a separated vessel, leads to unacceptably high removal of especially volatile working fluids, including CO2, amines, and solvents such as acetone. Therefore, a solution is desired which allows the removal of air/non-condensable gas partly at higher pressure than prevailing in the absorber section, this in order to increase the condensation of volatile working fluid, partly at lower temperature than prevailing in the absorber section, also in order to favour condensation of working fluid, and partly at minimum costs, i.e. with minimum or no investment costs especially for vacuum pumps.
- Some modifications and specific embodiments of the C3 process are disclosed in documents mentioned below, all of which are included by reference.
- A vessel in which e.g. CO2 working fluid is absorbed is separated by valves from a power generation process, in particular C3 as described in WO 2012/128 715 and SE 2013/051 059, SE 1300 576-4, SE 1400 027-7 and SE 1400 160-6, hereby incorporated by reference, but also standard ORC solutions based on one or more volatile working fluids such as lower paraffins, classic refrigerants and in general ORC working fluids with boiling points at atmospheric pressure below 100.degree. C. In standard operation, said vessel may function as absorption chamber where CO2 gas is absorbed by amines. During an ejection cycle for non-condensable gas, residual gas comprising CO2, non-condensable gas, water and alkaline materials including amines may be compressed by raising the liquid level in said vessel. The concurrent pressure increase leads to the selective absorption of CO2 by alkaline materials. In this way, the concentration of volatile amines in the gas space is reduced. Following the compression to above atmospheric pressure, non-condensable gas may be vented, optionally through a filter or a membrane in order to absorb remaining volatile amine. Optionally, a membrane or diaphragm may be used separating said vessel into two sections. Said membrane is permeable for air, but impermeable for volatile amines. Ideally, the membrane is not very permeable for CO2 gas. The membrane is ideally not in contact with liquid amine. Remaining or condensing liquid amine may be transferred back to the vessel, also without using a pump. The method is simple and economic as vacuum pumps may be omitted. However, using a vacuum pump is also considered an option for faster removal of non-condensable gases.
- The invention will now be described by way of non-limiting examples with reference to the accompanying drawing, in which
-
FIG. 1 is a schematic drawing of an arrangement highly suitable for the removal of at least one gas from a closed loop process involving one or two working fluids which are condensed rather than chemically absorbed, further showing how the gas removal unit is integrated into the complete power generation process. - This invention concerns in one aspect a method or procedure for the removal of at least one non-condensable gas from thermodynamic cycles, particularly from the C3 process mentioned above, which operates partly under vacuum, or ORC processes operating partly under vacuum.
- In one embodiment, the working fluid may comprise a low boiling solvent such as methanol, ethanol, acetone, isopropanol or butanol on the one hand at a concentration of at least 5% by weight, and ammonia as well as amines including diethylamine, dipropylamine, dibutylamine, and water-soluble amines including MEA, in water or organic solvents, such as disclosed in above mentioned documents and CO2. The procedures described below are suitable for the automatic and controlled removal air while the power generation cycle is in operation. Pressurizing leads to condensation of condensable gases, such as the solvents mentioned above. Despite this pressurizing step, a certain loss of volatile solvent or amine or CO2 is difficult to avoid but acceptable. Optionally, condensable components can be trapped outside the cycle by means known in the art, such that emissions to the environment are avoided.
- In a further aspect, now referring to
FIG. 1 , an absorption or condensation vessel 7 is in connection with a main absorbing or condensingvessel 50 through avalve 2 and a valve 4. Air removal is achieved in batch operation using the following sequence: - A) A valve 3 is opened to equilibrate the pressure in the condensation vessel 7 and the main condensing
vessel 50, while 2, 4 and 5 are closed. Condensed working fluid is drained through avalves line 19 into the main condensingvessel 50, prior to apump 51. Optionally, apump 24 is employed for working fluid transfer, e.g. if vessel 7 cannot be emptied by gravity. - B) The valve 4 is opened to start the spraying of cold condensed working fluid supplied through a
line 16. Thevalve 2 is opened to allow ingress of gas through aline 18 from the main condensingvessel 50 which in turn receives gas fromturbine 53. Pressures and temperatures are measured by sensors T8 and T9 and T10 as well as P12 and P14. - C) Working fluid condensation leads to a temperature increase, proportional to the condensation enthalpy of the working fluid and proportional to the amount of condensing working fluid. This temperature increase is lower in the condensation vessel 7 than in main condensing
vessel 50 partly due to the presence of accumulating non-condensable gases, and partly due to the fact that a higher liquid reflux ratio is used. As the batch sequence progresses, the temperature in the condensation vessel 7 may be 2-4.degree. C. lower than in main condensingvessel 50 for a situation where 90/20.degree. C. water is used for heating/cooling. The temperature difference T8−T9 should be around 30-700 of the corresponding difference T8−T10. If T8−T9 is approaching lower values (<30% of T8−T10), this may be taken as practical indication that no more gaseous working fluid is condensed in the condensation vessel 7. (Note that the given percentage levels are indicative only.) At that stage, thevalves 2 and 3 are closed whereas the valve 4 remains open such that working fluid supply through thesupply line 16 continues. Part of the remaining gaseous working fluid is condensed due to continued liquid flow and compression of the gas space which is now isolated, and the liquid level in the condensation vessel 7 rises. Afurther pump 13 may be provided for manipulating the absorption liquid level in said at least one absorption or condensation chamber 7. - D) The valve 4 is closed as soon as the pressure P12 in the condensation vessel 7 is close to or equal to the liquid pressure P11 in the
supply line 16 from a cooler 54. - E) The
valve 5 is opened such that apump 20 can supply liquid to the condensation vessel 7. The concurrent pressure increase leads to further condensation of gaseous working fluid. - F) As the pressure in the condensation vessel 7 is approaching the pressure P14 in a
supply line 17 which in turn is fed from thesupply line 16, the valve 1 is opened to release non-condensable gas through optionalsecondary vessel 22,optional valve 21 and ventline 23.Vessel 22 may serve as collection or recovery vessel for solvent if required. It is intended to eject as much air as possible, therefore, as a technical option, liquid supply throughsupply line 17 andvalve 5 can continue until the liquid level in the condensation vessel 7 reaches a specified level. Ejection of liquid can be prevented by known methods, e.g. a floating device (not shown inFIG. 1 ) which blocks the valve 1 if the liquid level is at the maximum level. Diaphragms or membranes essentially impermeable to gases other than oxygen, nitrogen and argon are used e.g. in saidsecondary vessel 22 to avoid the loss of process gas, notably CO2 and volatile solvent and amine. - G) Step A is repeated.
- At a starting time of release of non-condensable gas(es) from said at least one absorption or condensation chamber 7, the pressure in said at least one absorption or condensation chamber is at least 10%, preferably at least 30%, more preferably at least 80%, and most preferably even 150% higher than the pressure in a main absorption or condensation vessel (50).
- In the embodiment described above, it appears that the driving force enabling gas separation and subsequent ejection from the closed loop process is the temperature difference between (one or more) condensation vessel(s) 7 and the main absorption or condensation vessel(s) 50. This temperature difference is caused by the fact that liquid working fluid is pumped into the condensation vessel 7 at a higher rate, relative to the flow rate of gaseous working fluid, than into the
main absorption vessel 50. Therefore the liquid in the condensation vessel 7 is generally colder than in themain absorption vessel 50. Gaseous working fluid and non-condensable gas is entering the condensation vessel 7. The condensation of main working fluid leads to the enrichment of non-condensable gas in agas space 6 which further causes the temperature to drop in the condensation vessel 7. At a certain stage, it is practical to start sequence (C) described above. - As described, the fact that liquid in the condensation vessel 7 is colder than at any other stage in the process, is driving the gas separation. Cooling may be affected by the higher liquid flow rate, or alternatively by active cooling. The former method is using less energy, the latter method may be chosen in embodiments where e.g. space requirements dictate so.
- Referring further to
FIG. 1 , also the complete closed-loop process is shown, here as a simple Rankine process with aheat exchanger 52 for generation of hot gaseous working fluid, aturbine 53, themain condensation vessel 50, the temperature sensor T10 and a workingmedium pump 51. It should be appreciated that working fluid exiting from heat exchanger/absorber/condenser 50 i.e. themain absorption vessel 50 can be partly recycled to the top of the same, e.g. to achieve a lower average temperature in saidmain absorption vessel 50 or to aid absorption in themain absorption vessel 50. - In one of the preferred embodiments, acetone is used as working fluid. The solubilities of resp. oxygen and nitrogen are very low in acetone (see Battino, J. Phys. Chem. Ref.
Data Vol 12, No. 2, 1983, p. 174 and Vol. 13, No. 2, p. 587) such that air removal from acetone even at low temperature (e.g. between 20-40.degree. C. is efficient. Compared to prior-art solutions, loss of acetone or working fluid is significantly reduced. - In one embodiment, the gas mixture ejected from the process, comprising non-condensable gas(es) and minor amounts of solvents including acetone, isopropanol, amines or the like is prevented from entering the environment by use of a cold trap, suitable filters such as carbon black, zeolites or other absorbents, a scrubber or a burning/flaring unit.
- In one embodiment, removal of non-condensable gases may be automatically controlled e.g. by a software, whereby gas removal is triggered by one or more process sensor (T8, T9, T10 and P11, P12 and P14) indicating ingress or presence of non-condensable gas, specifically using temperature and pressure sensors (T8, T9, T10 and P11, P12 and P14), directly or indirectly indicating presence of non-condensable gas.
- The method described is also useful for air removal from a) steam-based Rankine cycles partly under vacuum but also from b) high pressure ORC systems. In case a) the method would be used to save costs, e.g. for a vacuum pump, in case b) this is relevant because already low air concentrations deteriorate the performance of heat exchangers such as condensers for ORC working fluids. Air ingress cannot be excluded despite the use of higher than atmospheric pressures.
- In a different embodiment, the technique for gas removal described above is used in a heat pump system. Essentially, in a heat pump a separate gas compression step is used to generate higher temperatures, e.g. for house heating purposes, from low value heat sources. Suitable heat pump designs operating partly under vacuum are disclosed in SE 1300576-4 assigned to Climeon AB and related disclosures.
- It should be understood that above embodiments are merely examples of useful sequences to achieve the objective of the invention, namely to remove non-condensable gases from a closed loop process representing a thermodynamic cycle, specifically the C3 cycle or any Rankine cycle operating partly under vacuum.
- Similar arrangements should be seen as falling under the spirit of this invention. In particular, diaphragms or membranes may be included to further reduce the loss of volatile materials such as amines, however, such solutions will be used depending on costs/benefits calculations.
- In summary, a simple solution is disclosed for removal of non-condensable gases from closed-loop-processes. The solution is cheap in construction and operation, and can be operated at any time while the thermodynamic cycle is operated, i.e. no stand-still is required.
- The methods disclosed here can be used in combination with closed-loop processes comprising working gas and chemicals as temporary and reversible working gas absorption agents. Specifically, the methods can be used combination with the C3 thermodynamic cycle comprising CO2 as working gas and amines as temporary and reversible CO2 absorption agents. Further use is possible in combination with a thermodynamic cycle comprising paraffins such as propane, butane, pentane, hexane, and its isomers, alcohols such as methanol, ethanol, isopropanol, butanol or ketones such as acetone or refrigerants e.g. containing fluorine atoms or water as working gas at a concentration of at least 10% by weight.
- Finally, the methods can be used in combination with a heat pump or refrigeration system, preferably operating partly under vacuum.
Claims (9)
1. A gas removal unit for removing non-condensable gases from a system implementing a closed-loop thermodynamic process involving a condensable working medium, the system including (i) a heat exchanger for generation of a hot gaseous working medium and (ii) a main condensation vessel/heat exchanger for condensation of the condensable working medium from the hot gaseous working medium to a condensed working medium, the gas removal unit comprising:
a vent line;
a first valve connected to the vent line; and
a condensation vessel connected to:
the vent line through which the non-condensable gases are to be released via the first valve; and
the main condensation vessel/heat exchanger through a second valve, a third valve and a fourth valve,
wherein the third valve and the fourth valve allow ingress of a condensed working medium from the main condensation vessel/heat exchanger into the condensation vessel, and
wherein the second valve allows ingress of a gaseous working medium from the closed-loop thermodynamic process into the condensation vessel.
2. The gas removal unit according to claim 1 , wherein the fourth valve allows the ingress of the condensed working medium from the main condensation vessel/heat exchanger into the condensation vessel as a spray.
3. The gas removal unit according to claim 1 , further comprising:
a first temperature sensor that monitors a first temperature in the condensation vessel;
a second temperature sensor that monitors a second temperature in the main condensation vessel/heat exchanger;
a third temperature sensor that monitors a third temperature in the condensed working medium before the condensed working medium is supplied into the condensation vessel as a spray; and
a first pressure sensor that monitors a first gas pressure in the condensation vessel.
4. The gas removal unit according to claim 1 , further comprising a cooler for actively cooling the condensed working medium entering into the condensation vessel from the main condensation vessel/heat exchanger.
5. The gas removal unit according to claim 1 ,
wherein the gas removal unit is connected with the vent line, and
wherein the gas removal unit comprises diaphragms or membranes essentially impermeable to gases other than the non-condensable gases and a cold trap.
6. The gas removal unit according to claim 1 ,
wherein the gas removal unit is connected with the vent line, and
wherein the gas removal unit comprises diaphragms or membranes essentially impermeable to gases other than the non-condensable gases and a filter.
7. The gas removal unit according to claim 1 ,
wherein the gas removal unit is connected with the vent line, and
wherein the gas removal unit comprises diaphragms or membranes essentially impermeable to gases other than the non-condensable gases and a scrubber.
8. The gas removal unit according to claim 1 ,
wherein the gas removal unit is connected with the vent line, and
wherein the gas removal unit comprises diaphragms or membranes essentially impermeable to gases other than the non-condensable gases and a burning/flaring unit.
9. A non-condensable gases removal system comprising:
a system implementing a closed-loop thermodynamic process involving a condensable working medium, the system comprising:
a heat exchanger for generation of a hot gaseous working medium; and
a main condensation vessel/heat exchanger for condensation of the condensable working medium from the hot gaseous working medium to a condensed working medium; and
a gas removal unit comprising:
a vent line;
a first valve connected to the vent line; and
a condensation vessel connected to:
the vent line through which the non-condensable gases are to be released via the first valve; and
the main condensation vessel/heat exchanger through a second valve, a third valve and a fourth valve,
wherein the third valve and the fourth valve allow ingress of a condensed working medium from the main condensation vessel/heat exchanger into the condensation vessel,
wherein the second valve allows ingress of a gaseous working medium from the system into the condensation vessel, and
whereby (i) the third valve can be open to equilibrate the pressure in the condensation vessel and the main condensation vessel/heat exchanger, (ii) the fourth valve can be open to start a spraying of a condensed working medium from the main condensation vessel/heat exchanger into the condensation vessel, and measuring a first temperature in the condensation vessel and a second temperature in the main condensation vessel/heat exchanger, (iii) the third valve can be closed to separate the main condensation vessel/heat exchanger from the condensation vessel, while the fourth valve remains open to supply the condensed working medium to the condensation vessel, such that a level of the condensed working medium in the condensation vessel rises, (iv) the fourth valve can be closed to stop the supply of the condensed working medium to the condensation vessel, and (v) the first valve can be open to release and remove non-condensable gases through the vent line.
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| US201615301350A | 2016-09-30 | 2016-09-30 | |
| US16/595,199 US20200200483A1 (en) | 2014-04-04 | 2019-10-07 | Removal of non-condensable gases from a closed loop process |
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Also Published As
| Publication number | Publication date |
|---|---|
| WO2015152796A1 (en) | 2015-10-08 |
| US10436518B2 (en) | 2019-10-08 |
| JP2017512941A (en) | 2017-05-25 |
| EP3126756A1 (en) | 2017-02-08 |
| EP3126756A4 (en) | 2017-11-08 |
| JP6778177B2 (en) | 2020-10-28 |
| EP3364131A1 (en) | 2018-08-22 |
| US20170122670A1 (en) | 2017-05-04 |
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