WO2015159894A1 - 冷熱利用システム、冷熱利用システムを備えるエネルギシステム、及び冷熱利用システムの利用方法 - Google Patents
冷熱利用システム、冷熱利用システムを備えるエネルギシステム、及び冷熱利用システムの利用方法 Download PDFInfo
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- 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
- F01K25/10—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 the vapours being cold, e.g. ammonia, carbon dioxide, ether
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- 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
- F01K23/00—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids
- F01K23/02—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids the engine cycles being thermally coupled
- F01K23/04—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids the engine cycles being thermally coupled condensation heat from one cycle heating the fluid in another cycle
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- 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
- F01K9/00—Plants characterised by condensers arranged or modified to co-operate with the engines
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02C—GAS-TURBINE PLANTS; AIR INTAKES FOR JET-PROPULSION PLANTS; CONTROLLING FUEL SUPPLY IN AIR-BREATHING JET-PROPULSION PLANTS
- F02C1/00—Gas-turbine plants characterised by the use of hot gases or unheated pressurised gases, as the working fluid
- F02C1/02—Gas-turbine plants characterised by the use of hot gases or unheated pressurised gases, as the working fluid the working fluid being an unheated pressurised gas
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C7/00—Methods or apparatus for discharging liquefied, solidified, or compressed gases from pressure vessels, not covered by another subclass
- F17C7/02—Discharging liquefied gases
- F17C7/04—Discharging liquefied gases with change of state, e.g. vaporisation
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C9/00—Methods or apparatus for discharging liquefied or solidified gases from vessels not under pressure
- F17C9/02—Methods or apparatus for discharging liquefied or solidified gases from vessels not under pressure with change of state, e.g. vaporisation
- F17C9/04—Recovery of thermal energy
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2221/00—Handled fluid, in particular type of fluid
- F17C2221/03—Mixtures
- F17C2221/032—Hydrocarbons
- F17C2221/033—Methane, e.g. natural gas, CNG, LNG, GNL, GNC, PLNG
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2223/00—Handled fluid before transfer, i.e. state of fluid when stored in the vessel or before transfer from the vessel
- F17C2223/01—Handled fluid before transfer, i.e. state of fluid when stored in the vessel or before transfer from the vessel characterised by the phase
- F17C2223/0146—Two-phase
- F17C2223/0153—Liquefied gas, e.g. LPG, GPL
- F17C2223/0161—Liquefied gas, e.g. LPG, GPL cryogenic, e.g. LNG, GNL, PLNG
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2225/00—Handled fluid after transfer, i.e. state of fluid after transfer from the vessel
- F17C2225/01—Handled fluid after transfer, i.e. state of fluid after transfer from the vessel characterised by the phase
- F17C2225/0107—Single phase
- F17C2225/0123—Single phase gaseous, e.g. CNG, GNC
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2225/00—Handled fluid after transfer, i.e. state of fluid after transfer from the vessel
- F17C2225/03—Handled fluid after transfer, i.e. state of fluid after transfer from the vessel characterised by the pressure level
- F17C2225/035—High pressure, i.e. between 10 and 80 bars
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/01—Propulsion of the fluid
- F17C2227/0128—Propulsion of the fluid with pumps or compressors
- F17C2227/0135—Pumps
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/01—Propulsion of the fluid
- F17C2227/0128—Propulsion of the fluid with pumps or compressors
- F17C2227/0171—Arrangement
- F17C2227/0178—Arrangement in the vessel
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/03—Heat exchange with the fluid
- F17C2227/0302—Heat exchange with the fluid by heating
- F17C2227/0309—Heat exchange with the fluid by heating using another fluid
- F17C2227/0316—Water heating
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/03—Heat exchange with the fluid
- F17C2227/0302—Heat exchange with the fluid by heating
- F17C2227/0309—Heat exchange with the fluid by heating using another fluid
- F17C2227/0316—Water heating
- F17C2227/0318—Water heating using seawater
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2227/00—Transfer of fluids, i.e. method or means for transferring the fluid; Heat exchange with the fluid
- F17C2227/03—Heat exchange with the fluid
- F17C2227/0367—Localisation of heat exchange
- F17C2227/0388—Localisation of heat exchange separate
- F17C2227/0393—Localisation of heat exchange separate using a vaporiser
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2265/00—Effects achieved by gas storage or gas handling
- F17C2265/06—Fluid distribution
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2265/00—Effects achieved by gas storage or gas handling
- F17C2265/07—Generating electrical power as side effect
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E20/00—Combustion technologies with mitigation potential
- Y02E20/16—Combined cycle power plant [CCPP], or combined cycle gas turbine [CCGT]
Definitions
- the present invention relates to a cold energy utilization system that uses cold energy of a low-temperature liquefied gas stored in a storage tank, an energy system that includes the cold energy utilization system, and a method of using the cold energy utilization system.
- LNG liquefied natural gas
- Liquefied natural gas is obtained by cooling natural gas (NG) produced in a foreign production area using electric power and liquefying it.
- the liquefied natural gas that has been liquefied and reduced in volume is imported by an LNG transport tanker.
- the liquefied natural gas is usually vaporized by an open rack type vaporizer or the like at an import site.
- the heat and energy of the liquefied natural gas is discarded in the seawater by exchanging heat between the liquefied natural gas and the seawater.
- FIG. 15 shows the result of estimating the cold utilization of liquefied natural gas imported into Japan in one year. Most of the thermal energy is not recovered but discarded.
- a cold energy utilization system that utilizes the cold energy of liquefied natural gas is known.
- a cold power generation system is known as a cold heat utilization system.
- an existing thermal power generation system there are a Rankine cycle system, a direct expansion system, and a combination thereof.
- the Rankine cycle method condenses a working fluid (intermediate medium) such as hydrocarbons or chlorofluorocarbons by the cold heat of liquefied natural gas in a condenser, and vaporizes the condensed working fluid in a vaporizer. Then, power is generated by driving the turbine with the vaporized working fluid.
- a working fluid such as hydrocarbons or chlorofluorocarbons
- power is generated by driving the turbine with the vaporized working fluid.
- liquefied natural gas is vaporized in a vaporizer, and power is generated by driving a turbine with the vaporized natural gas.
- the combined use type cooling and power generation system is a combination of the Rankine cycle method and the direct expansion method as seen in, for example, Patent Documents 1 and 2 below.
- the combined system has a higher recovery rate of effective chilled natural gas energy (cold energy) and higher power generation capacity than the Rankine cycle system and the direct expansion system, respectively.
- the liquefied natural gas chilling exergy (effective energy) is directly expanded by the temperature exergy that condenses the working fluid circulating in the Rankine cycle and the natural gas vaporized by heat exchange with the working fluid. It is used as pressure exergy to drive a turbine of the type.
- FIG. 16 is the figure which illustrated the part which can utilize the cold heat exergy for every LNG import base in the conventional cold energy utilization system.
- FIG. 17 is a record table of the cold power generation system
- FIG. 18 is a diagram illustrating a relationship between the gas delivery pressure and the power generation unit of the cold power generation in FIG. As shown in FIGS. 17 and 18, the power generation unit tends to decrease as the gas delivery pressure increases.
- the gas delivery pressure has increased due to the widespread use of gas turbine combined cycle power generation in the electricity business and the increase in gas delivery volume in the gas business. For this reason, the ratio which is converted into the pressure exergy of the delivery gas in the cold exergy of liquefied natural gas increases, and the cold energy exergy that can be converted into electric power in the cold power generation system tends to decrease. As a result, the amount of power generated by the cold power generation system tends to decrease, and the cold power generation system is not widespread.
- a booster pump that pressurizes a low-temperature liquefied gas stored in a storage tank to a predetermined pressure while being in a liquid state, and heats the liquefied gas boosted by the booster pump and a predetermined cold heat exchange target.
- a primary device having a vaporizer that cools the cold heat exchange target and vaporizes the liquefied gas, and a secondary turbine driven by the vaporized gas that is the liquefied gas vaporized in the vaporizer
- a process start point (C1) that defines the pressure and temperature of the gas stored in the storage tank on the Mollier diagram of the gas to be stored in the storage tank.
- the point defining the predetermined pressure and temperature of the gas on the inlet side of the vaporizer is preovered.
- the boost point (C2) is defined, and on the Mollier diagram, the turbine inlet point (C3), which is the point defining the pressure and temperature of the gas on the inlet side of the secondary turbine, or the outlet side of the carburetor Is defined as an intermediate point, and on the Mollier diagram, the point that defines the pressure and temperature of the gas at the outlet side of the secondary turbine is defined as an intermediate point.
- a turbine outlet point (C4) is defined, and a value obtained by subtracting the enthalpy at the process start point from the enthalpy at the preover boost point is defined as a first enthalpy difference ( ⁇ h1), and the preover boost from the enthalpy at the intermediate point
- the value obtained by subtracting the enthalpy at the point is defined as the second enthalpy difference ( ⁇ h2; ⁇ h2rank).
- the work performed by the secondary turbine from the state at the turbine inlet point (C3), which is the point that defines the pressure and temperature of the gas on the inlet side of the secondary turbine, to the state at the turbine outlet point is determined as a third enthalpy.
- ⁇ h3 Carnot defined as a difference ( ⁇ h3) and determined by a value obtained by subtracting the first enthalpy difference from an addition value of the second enthalpy difference and the third enthalpy difference, or a temperature of each of the preover boost point and the intermediate point
- the predetermined pressure is equal to the total enthalpy difference. Characterized in that it is Zui to set.
- the low-temperature liquefied gas stored in the storage tank is boosted by a booster pump while being in a liquid state up to a predetermined pressure.
- the vaporizer which comprises a primary apparatus
- prescribed cold-heat exchange object (intermediate medium) are heat-exchanged.
- the cold heat exchange object is cooled, and the liquefied gas is vaporized to become a vaporized gas.
- the secondary turbine which comprises a secondary apparatus is driven with the vaporization gas which flowed out from the vaporizer.
- the cold exergy of the low-temperature liquefied gas stored in the storage tank is used as a temperature exergy for cooling the cold heat exchange target in the primary device and a pressure exergy for driving the turbine in the secondary device.
- the inventor of the present application uses the total enthalpy difference based on the first enthalpy difference, the second enthalpy difference, and the third enthalpy difference in order to grasp the utilization efficiency of the liquefied gas cooling heat energy.
- the total enthalpy difference indicates that the higher the value is, the higher the utilization efficiency of the liquefied gas for cold heat exergy.
- the total enthalpy difference depends on the gas pressure at the pre-over boost point, and by setting the pressure at the pre-over boost point corresponding to the total enthalpy difference, which increases the use efficiency of the cold heat energy, to the predetermined pressure.
- the utilization efficiency of cold heat exergy can be increased. In view of this point, in the present invention, it is possible to increase the utilization efficiency of the cold heat energy by setting the predetermined pressure based on the total enthalpy difference.
- the gas delivery pressure on the secondary turbine outlet side increases.
- the gas delivery pressure on the secondary turbine outlet side can be freely set and controlled.
- the cold energy utilization system of the present invention can be embodied as follows, for example.
- the cold energy utilization system includes a booster pump that boosts a low-temperature liquefied gas stored in a storage tank to a predetermined pressure equal to or higher than the critical pressure in a liquid state, and the liquefied gas boosted by the booster pump and the predetermined pressure.
- a booster pump that boosts a low-temperature liquefied gas stored in a storage tank to a predetermined pressure equal to or higher than the critical pressure in a liquid state
- 1 having a vaporizer that cools the cold heat exchange target and vaporizes the liquefied gas by exchanging heat with the cold heat exchange target (intermediate medium) while maintaining the pressure of the liquefied gas at the critical pressure or higher.
- a secondary device having a secondary turbine driven by the vaporized gas that is the liquefied gas vaporized in the vaporizer.
- the step of vaporizing the liquefied gas in the vaporizer while maintaining the state at or above the critical pressure is for efficiently using the cold energy exergy of the liquefied gas. More specifically, the larger the difference between the enthalpy of the liquefied gas at the vaporization process inlet (C2) and the enthalpy of the vaporized gas at the vaporization process outlet (C3 or CA), the larger the cold energy exergy of the liquefied gas used in the primary device. The rate of conversion to temperature exergy increases.
- the recovery of the cold exergy using the vaporizer of the primary device involves heat transfer.
- the recovery rate of cold exergy accompanied by heat transfer is lower than the efficiency of recovering cold exergy by driving the secondary turbine with gas pressure exergy. For this reason, when the ratio converted into the temperature exergy used in the primary device in the cold exergy of the liquefied gas is increased, the utilization efficiency of the cold exergy is reduced.
- the pressure of the liquefied gas to be equal to or higher than the critical pressure
- the enthalpy of the liquefied gas after the vaporization process inlet for example, the enthalpy in the boiling curve of the Mollier diagram
- the enthalpy of the vaporized gas at the vaporization process outlet for example, The difference (so-called latent heat of vaporization) from the enthalpy in the condensation curve of the Mollier diagram becomes small.
- the utilization efficiency of the liquefied gas cold exergy can be enhanced as viewed from the whole cold utilization system.
- the figure which shows the outline of a cold energy power generation system The figure which shows the outline of the cold power generation process on a Mollier diagram.
- Calculation result of equation (1) “ ⁇ h2 + ⁇ h3 ⁇ h1” when the secondary expansion turbine inlet temperature (T3) is 20 ° C.
- the Mollier diagram for demonstrating the definition of 2nd enthalpy difference (DELTA) h2rank concerning other embodiment.
- the calculation result of Formula (4) “ ⁇ ⁇ ⁇ h2rank + ⁇ h3 ⁇ h1” when the secondary expansion turbine inlet temperature (T3) according to another embodiment is 20 ° C.
- the calculation result of Formula (4) “ ⁇ ⁇ ⁇ h2rank + ⁇ h3 ⁇ h1” when the secondary expansion turbine inlet temperature (T3) according to another embodiment is 50 ° C.
- the cold power generation system generates power using the cold heat of liquefied natural gas (LNG) stored in the storage tank 10.
- LNG liquefied natural gas
- an example is shown in which the cold power generation system is applied to a vaporizer that vaporizes liquefied natural gas stored in the storage tank 10 and sends it to the outside as natural gas (NG).
- NG natural gas
- the liquefied natural gas stored in the storage tank 10 is pressurized by the primary pump 11 and supplied to the secondary pump 12.
- the supplied liquefied natural gas is further pressurized by the secondary pump 12.
- the liquefied natural gas pressurized by the secondary pump 12 is supplied to the first vaporizer 13 and the tertiary pump 14.
- the first vaporizer 13 heats and vaporizes the liquefied natural gas by exchanging heat between the liquefied natural gas supplied from the secondary pump 12 and the heat medium.
- an open rack type vaporizer ORV
- normal temperature water is used as a heat medium in the first vaporizer 13.
- the tertiary pump 14 is a booster pump that further boosts the liquefied natural gas supplied from the secondary pump 12 to the pre-over boost pressure.
- the liquefied natural gas boosted by the tertiary pump 14 is supplied to the main vaporizer 15.
- the main vaporizer 15 evaporates the liquefied natural gas into natural gas by exchanging heat between the supplied liquefied natural gas and the working fluid (intermediate medium) of the Rankine cycle.
- a shell and tube type vaporizer (STV) is used as the main vaporizer 15.
- petroleum gas (PG) is used as the working fluid (intermediate medium).
- the main vaporizer 15 constitutes a Rankine cycle primary power generator.
- the primary power generator includes a circulation pump 16, an intermediate medium evaporator 17, and a primary turbine generator 18 in addition to the main vaporizer 15.
- the main vaporizer 15 functions as a condenser that condenses the working fluid by cooling the working fluid circulating in the Rankine cycle with the liquefied natural gas pressurized by the tertiary pump 14.
- the working fluid (intermediate medium) condensed in the main vaporizer 15 is supplied to the intermediate medium evaporator 17 by the circulation pump 16.
- the intermediate medium evaporator 17 vaporizes the working fluid by exchanging heat between the low-temperature working fluid and the heat medium.
- STV is used as the intermediate medium evaporator 17
- normal temperature water (seawater) or hot water having a temperature higher than that of normal temperature water is used as the heat medium in the intermediate medium evaporator 17.
- the hot water is generated by, for example, waste heat energy of a nearby factory.
- the working fluid vaporized in the intermediate medium evaporator 17 flows into the primary expansion turbine of the primary turbine generator 18 and drives the primary expansion turbine.
- the generator of the primary turbine generator 18 generates power by driving the primary expansion turbine.
- the primary power generation device generates power by using the cold natural exergy of the liquefied natural gas stored in the storage tank 10 as the temperature exergy.
- the natural gas flowing out from the main vaporizer 15 is supplied to the first heater 19.
- the first heater 19 heats the natural gas to increase the temperature by exchanging heat between the supplied natural gas and the heat medium.
- a heat medium in the 1st heater 19 normal temperature water (seawater) or warm water can be used, for example.
- the natural gas heated in the first heater 19 flows into the secondary expansion turbine of the secondary turbine generator 20 and drives the secondary expansion turbine.
- the generator of the secondary turbine generator 20 generates electric power by driving the secondary expansion turbine. In this way, by using the cold natural exergy of liquefied natural gas as the pressure exergy, the direct expansion type secondary power generator generates power.
- FIG. 1 shows a configuration with only one secondary expansion turbine, the configuration is not limited to this.
- a multi-stage expansion type configuration in which a secondary expansion turbine and a heater for reheating gas flowing out from the secondary expansion turbine are alternately connected may be used.
- the natural gas flowing out from the secondary expansion turbine of the secondary turbine generator 20 is supplied to the second heater 21.
- the second heater 21 heats the natural gas and raises the temperature by exchanging heat between the natural gas and the heat medium.
- the natural gas heated in the second heater 21 and the natural gas vaporized in the first vaporizer 13 merge and are sent out to the gas conduit as city gas, for example. Thereby, natural gas is supplied to an external supply destination.
- carburetor 13 may be sent to each of independent gas conduits, without joining.
- This setting method is based on the following formula (1), formula (3), or formula (4) depending on the embodiment.
- ⁇ htotal ⁇ h2 + ⁇ h3 ⁇ h1 (1)
- ⁇ h1 is referred to as a first enthalpy difference
- ⁇ h2 is referred to as a second enthalpy difference
- ⁇ h3 is referred to as a third enthalpy difference
- ⁇ htotal is referred to as a total enthalpy difference.
- each operation point of the cold utilization process (cold power generation process) in the Mollier diagram shown in FIG. 2 will be described first.
- the state of the liquefied natural gas stored in the storage tank 10 is indicated by a first point C1
- the state of the liquefied natural gas boosted by the tertiary pump 14 is indicated by a second point C2.
- the state of the natural gas at the inlet of the secondary expansion turbine of the secondary turbine generator 20 is indicated by a third point C3, and the state of the natural gas at the outlet of the secondary expansion turbine is indicated by a fourth point C4.
- the state of the natural gas at the outlet of the two heater 21 is indicated by a fifth point C5.
- the pressure and temperature at the first point C1 are defined as the first pressure P1 and the first temperature T1
- the pressure at the second point C2 is defined as the second pressure P2.
- the transition of the operating point from the first point C1 to the second point C2 follows an isentropic change (adiabatic compression). Further, the pressure and temperature at the third point C3 are defined as a third pressure P3 and a third temperature T3. In the present embodiment, the transition of the operating point from the second point C2 to the third point C3 follows a constant pressure change. For this reason, the third pressure P3 and the second pressure P2 are equal.
- the pressure and temperature at the fourth point C4 are defined as a fourth pressure P4 and a fourth temperature T4. Further, the pressure and temperature at the fifth point C5 are defined as a fifth pressure P5 and a fifth temperature T5.
- the fifth temperature T5 and the third temperature T3 are equal.
- the first enthalpy difference ⁇ h1 is defined as a value obtained by subtracting the specific enthalpy at the first point C1 from the specific enthalpy at the second point C2.
- the second enthalpy difference ⁇ h2 is defined as a value obtained by subtracting the specific enthalpy at the second point C2 from the specific enthalpy at the third point C3.
- the third enthalpy difference ⁇ h3 is a secondary expansion from the third point C3 to the fourth point C4 so that the operating point does not enter the liquid phase side of the gas-liquid equilibrium curve B on the Mollier diagram.
- the condition that the operating point does not enter the liquid phase side of the gas-liquid equilibrium curve B on the Mollier diagram is that gas re-condensation is prevented and erosion or erosion of the secondary expansion turbine occurs. This is to avoid damage.
- FIG. 2 illustrates the case where four-stage expansion is performed.
- the hot water is used as the heat medium, and the natural gas is heated up to the third temperature T3 according to the isobaric change.
- the positional relationship between the object and the environmental temperature that is, the cryogenic liquefied gas is vaporized by the thermal energy of the environmental temperature without adding fuel, whereas the water vapor is vaporized by heating with the fuel. This is because the temperature is raised from the environmental temperature to a predetermined temperature.
- Cold energy temperature energy + pressure energy (2) Is converted.
- the temperature exergy recovery rate is lower than the pressure exergy recovery rate due to the restriction of the second law of thermodynamics (Carnot efficiency). Therefore, in order to increase the recovery rate of the cold heat energy, it is effective to convert the cold energy into pressure energy rather than temperature energy. That is, a method for converting cold energy into pressure energy more effectively is effective.
- a method of vaporizing the liquefied gas while being pressurized to a high pressure is appropriate. From the Mollier diagram of the liquefied gas, as the gas is vaporized at a higher pressure, the latent heat of vaporization of the liquefied gas becomes smaller and the enthalpy difference in the vaporization process becomes smaller, but the pressure exergy of the vaporized gas increases conversely.
- the total enthalpy difference ⁇ htotal represented by the above formula (1) takes a maximum value at a certain second pressure P2.
- the second pressure P2 corresponding to this maximum value to the pre-over boost pressure
- the pressure is an absolute pressure.
- FIG. 3 shows an example in which each parameter of natural gas in the pressure increasing process (isentropic change) from the first point C1 to the second point C2 is calculated using REFPROP.
- the critical point of the natural gas is indicated by A1
- the operating point at which the natural gas pressure becomes the crimpon denver is indicated by A2.
- the calculation result of the amount of natural gas that can be used by the natural gas having the above composition from ⁇ 162 ° C. to 20 ° C. was 906 kJ / kg.
- the first pressure P1 at the first point C1 was set to 0.101 MPa, and the first temperature T1 was set to ⁇ 162 ° C.
- the third temperature T3 is set to 20 ° C.
- room temperature water is used as the heat medium in the first heater 19 and the second heater 21.
- the first enthalpy difference ⁇ h1 is proportional to the second pressure P2. For this reason, as shown in FIG. 4A, the first enthalpy difference ⁇ h1 increases as the second pressure P2 increases.
- the transition line of the operating point from the first point C1 to the second point C2 is substantially parallel to the isenthalpy line (indicated by a one-dot chain line in FIG. 2). It becomes. For this reason, liquefied natural gas can be made into a high voltage
- the second enthalpy difference ⁇ h2 decreases as the second pressure P2 increases. This is because the specific enthalpy at the second point C2 increases as the second pressure P2 increases.
- the specific enthalpy of the third point C3 starts to increase around 42 MPa, but on the other hand, the specific enthalpy of the second point C2 also increases as the gas pressure increases. Therefore, as shown in FIG. 4B, the second enthalpy difference ⁇ h2 continues to decrease.
- the third enthalpy difference ⁇ h3 increases as the second pressure P2 increases. This is because the density of the gas flowing into the secondary expansion turbine increases as the second pressure P2 increases. In particular, the gradient of the increase in the third enthalpy difference ⁇ h3 with respect to the increase in the second pressure P2 until the second pressure P2 is close to the critical pressure is larger than the gradient when the second pressure P2 is higher than the critical pressure. . In addition, the third enthalpy difference ⁇ h3 increases as the fourth pressure P4 decreases. This is because the lower the outlet pressure of the secondary expansion turbine, the more work done by the secondary expansion turbine. FIG.
- FIG. 4C shows the calculation result of the third enthalpy difference ⁇ h3 when the fourth pressure P4 is set every 0.1 MPa in the range of 0.2 to 1.0 MPa.
- the third enthalpy difference ⁇ h3 becomes substantially the same value as the addition value of the second enthalpy difference ⁇ h2 and the first enthalpy difference ⁇ h1 as the second pressure P2 is increased ( ⁇ h3 ⁇ h1 + ⁇ h2).
- FIG. 5 shows the relationship between the total enthalpy difference ⁇ htotal calculated by substituting the first, second and third enthalpy differences ⁇ h1, ⁇ h2, and ⁇ h3 calculated by the above-described method into the above equation (1) and the second pressure P2. Show.
- the second pressure P2 indicating the highest conversion efficiency is specified by the total enthalpy difference ⁇ htotal.
- the second pressure P2 that maximizes the total enthalpy difference ⁇ htotal is specified as 6.8 MPa that is substantially close to the critical pressure.
- the second pressure P2 at which the total enthalpy difference ⁇ htotal is first maximized is specified as 6.8 MPa.
- the second pressure P2 indicating the highest conversion efficiency shows the same value even if the gas pressure at the fourth point C4 (the same value as the gas delivery pressure at the fifth point C5) is changed.
- FIG. 5 shows the calculation result of the total enthalpy difference ⁇ htotal when the fourth pressure P4 is set every 0.1 MPa in the range of 0.2 to 1.0 MPa.
- the value of the ⁇ 3 enthalpy difference h3 is calculated as the amount of exergy (Flow Exergy) of the third point C3 with the fifth point C5 as a reference point in this calculation. Since exergy is not a stored amount, it cannot generally be treated as the same amount of energy for state change. However, in the above formula (1), there is no problem because the total amount of energy at a specific process point is observed.
- the third temperature T3 is set to 50 ° C.
- hot water generated by exhaust heat energy is used as the heat medium of the first heater 19
- normal temperature water is used as the heat medium in the second heater 21.
- the first enthalpy difference ⁇ h1 increases as the second pressure P2 increases. Since the first enthalpy difference ⁇ h1 is determined by the specific enthalpies of the first point C1 and the second point C2, the calculation result of FIG. 6A is the same as the calculation result of FIG. is there.
- the second enthalpy difference ⁇ h2 decreases as the second pressure P2 increases, and the third enthalpy difference ⁇ h3 increases as shown in FIG. 6C. It gets bigger.
- FIG. 7 shows the relationship between the total enthalpy difference ⁇ htotal calculated by substituting the first, second, and third enthalpy differences ⁇ h1, ⁇ h2, ⁇ h3 calculated by the above-described method into the above equation (1) and the second pressure P2.
- the second pressure P2 indicating the highest conversion efficiency is specified by the total enthalpy difference ⁇ htotal.
- the second pressure P2 at which the total enthalpy difference is maximized is specified as 9.4 MPa which is equal to or higher than the critical pressure (and cricon denbar).
- the second pressure P2 indicating the highest conversion efficiency shows the same value even if the gas pressure at the fourth point C4 (the same value as the gas delivery pressure at the fifth point C5) is changed.
- the pre-over boost pressure indicating the maximum conversion efficiency is specified by the above equation (1), and the pre-over boost pressure indicating the maximum conversion efficiency is similarly specified even if the temperature of the vaporization heat source and the gas delivery pressure are changed. Is done.
- the pre-over-boost pressure that converts the liquefied gas cooling exergy into work (electric power) at maximum efficiency can be specified by specifying the two conditions of the composition of the liquefied gas and the temperature of the vaporization heat source. Yes.
- the final pressure at the system outlet vaporized gas delivery pressure
- the total enthalpy difference ⁇ htotal is determined, and the output (generated power) of the power generator of the entire system is specified. can do.
- FIG. 8 shows the total enthalpy difference ⁇ htotal of the above equation (3) calculated based on the enthalpy differences ⁇ h1, ⁇ h2, ⁇ h3 and the efficiency coefficient ⁇ of FIG. 4 when the third temperature T3 is 20 ° C. .
- the efficiency coefficient ⁇ is set to 0.621 which is the theoretical thermal efficiency of the Carnot cycle.
- the second pressure P2 at which the total enthalpy difference was the maximum was calculated as 9.7 MPa, which is a pressure equal to or higher than the klycon denvar, regardless of the magnitude of the fourth pressure P4. .
- 9.7 MPa a pressure equal to or higher than the klycon denvar
- FIG. 9 shows the total enthalpy difference ⁇ htotal of the above equation (3) calculated based on the enthalpy differences ⁇ h1, ⁇ h2, ⁇ h3 and the efficiency coefficient ⁇ of FIG. 4 when the third temperature T3 is 50 ° C.
- the second pressure P2 at which the total enthalpy difference ⁇ htotal is maximized is calculated as 14.1 MPa, which is a pressure equal to or higher than the Krykondenvar, regardless of the magnitude of the fourth pressure P4. It was. For this reason, when setting the 3rd temperature T3 to 50 degreeC, the trial calculation result that the power conversion efficiency of a thermal exergy was maximized was obtained by setting a preover boost pressure to 14.1 MPa.
- the present inventor uses the LNG supercritical pressure, cold, energy, power, generation (LSG) system as the LNG supercritical pressure, cold power generation system. I decided to call it.
- LSG LNG supercritical pressure, cold, energy, power, generation
- the third temperature T3 the second and third enthalpy differences ⁇ h2 and ⁇ h3 can be increased, and the temperature difference between the cooling and heating sources can be increased, and the theoretical thermal efficiency of the Carnot cycle can be increased. Can be high. As a result, it is possible to increase the power conversion efficiency of the cold heat energy in the LSG. Further, by increasing the third temperature T3, the number of stages of expansion and reheating from the third point C3 to the fourth point C4 can be reduced, and the equipment cost of the LSG can be reduced.
- the power conversion efficiency of the thermal exergy can be increased by setting the preover boost pressure using the concept of the total enthalpy difference ⁇ htotal. That is, the greater the difference ⁇ h2 between the enthalpy of liquefied natural gas at the natural gas vaporization process inlet (second point C2) and the natural gas enthalpy at the vaporization process outlet (third point C3), the greater the cold exergy of liquefied natural gas.
- the rate of conversion into temperature exergy used in the Rankine cycle primary power generator increases.
- the Rankine cycle includes an irreversible process of heat transfer.
- the recovery rate (for example, 20 to 30%) of the cold heat energy in the primary power generation apparatus is lower than the recovery rate (for example, 70 to 80%) of the cold heat energy in the direct expansion type secondary power generation apparatus. Therefore, from the above equation (2), if the ratio of the liquefied natural gas cooling exergy converted to the temperature exergy used in the primary power generator is increased, the power conversion efficiency of the cooling exergy will be reduced. Conversely, if the rate of conversion into temperature exergy is lowered, the power conversion efficiency of the cold heat exergy can be increased.
- the difference ⁇ h2 between the enthalpy of the liquefied natural gas at the vaporization process inlet of the main vaporizer 15 and the natural gas enthalpy at the vaporization process outlet is reduced by setting the preover boost pressure to a high pressure (for example, higher than the critical pressure). Therefore, the latent heat of vaporization of gas in the vaporization process (enthalpy between gas-liquid boundary lines in the Mollier diagram in FIG. 2) becomes small, and the latent heat of vaporization becomes invisible above the Krykon Denver pressure. Thereby, although the cold heat energy which is converted into temperature exergy decreases, the cold heat energy which is converted into pressure exergy increases.
- the power generation amount of the Rankine cycle primary power generation device is reduced, the power generation amount of the direct expansion type secondary power generation device having a higher recovery rate (power conversion rate) of cold heat exergy than the Rankine cycle method is to be increased. Can do. As a result, the power conversion efficiency of the liquefied natural gas cold heat energy can be increased when viewed from the whole cold power generation system.
- the natural gas is maintained in the main vaporizer 15 while maintaining the pressure of the natural gas higher than the CLICON denver. Will be vaporized. Thereby, the power conversion efficiency of cold heat energy can further be improved. That is, the liquefied natural gas that is a non-azeotropic mixture is condensed if the pressure is higher than the critical pressure but less than the cricon denver. Therefore, by setting the preover boost pressure to a pressure equal to or higher than the crimpon denver, the liquefied natural gas is vaporized without going through the gas-liquid mixed phase in the vaporization step.
- the latent heat of vaporization of the liquefied natural gas is not seen in the vaporization step, and the latent heat of vaporization of the liquefied natural gas used for condensation of the working fluid circulating in the Rankine cycle can be reduced. Therefore, compared with the structure which vaporizes liquefied natural gas through a gas-liquid mixed phase, the cold-heated exergy converted into temperature exergy can be decreased more. As a result, it is possible to further increase the cold heat energy that is converted into pressure exergy, and to further increase the power conversion efficiency of the cold heat energy of the entire system.
- FIG. 10 shows a natural gas liquefaction process (LNG) together with the cold power generation process (LSG) according to the present embodiment.
- LNG natural gas liquefaction process
- LSG cold power generation process
- the liquefaction process is pressurized after the natural gas is pressurized to near the critical pressure to avoid the gas-liquid mixing region, and then cooled, so multi-stage compression (Adiabatic Compression), precooling (Precooling), liquefaction (Liquefaction), supercooling ( Subcooling) and Joule-Thomson Throttling.
- the efficiency coefficient ⁇ used for calculating the total enthalpy difference is the Carnot cycle's theoretical thermal efficiency, but is not limited thereto, and the efficiency coefficient ⁇ is set to 0 according to the specifications of the LSG to be calculated. And may be set to a value less than the theoretical thermal efficiency.
- the cold energy of the liquefied natural gas is converted into mechanical energy that drives the primary expansion turbine of the primary power generator.
- the cold energy may be used as it is, and may be converted into energy for cooling the refrigerated warehouse or producing liquefied carbon dioxide.
- the second enthalpy difference ⁇ h2 may be defined as a value obtained by subtracting the specific enthalpy at the second point C2 from the specific enthalpy at the third point C3 without using the efficiency coefficient ⁇ .
- the second enthalpy difference is defined as a value obtained by subtracting the specific enthalpy at the second point C2 from the specific enthalpy at the third point C3.
- the present invention is not limited to this, and is defined as described below, for example. Also good.
- the state of natural gas at the outlet of the main vaporizer 15 is indicated by point A CA.
- the second enthalpy difference ⁇ h2rank may be defined as a value obtained by subtracting the specific enthalpy at the second point C2 from the specific enthalpy at the A point CA.
- the total enthalpy difference ⁇ htotal in this case is expressed by the following equation.
- the efficiency coefficient ⁇ is defined as a value that is equal to or lower than the theoretical thermal efficiency of the Carnot cycle determined by each of the second temperature T2 at the second point C2 and the gas temperature at the A point CA and is greater than zero.
- the working fluid in the Rankine cycle of the primary power generator is, for example, LPG (propane)
- the temperature at the point A is set to, for example, ⁇ 44 ° C.
- FIG. 12 shows the total enthalpy calculated by substituting the first and third enthalpy differences ⁇ h1 and ⁇ h3 and the second enthalpy difference ⁇ h2rank in FIG. 4 into the above equation (4) when the third temperature T3 is 20 ° C.
- the relationship between the difference ⁇ htotal and the second pressure P2 is shown. Further, in FIG.
- the third temperature T3 when the third temperature T3 is set to 20 ° C., the total enthalpy of the above equation (4) is increased when the second pressure P2 is increased from 0 regardless of the magnitude of the fourth pressure P4.
- the second pressure P2 at which the difference ⁇ htotal first reached a maximum was calculated as 6.0 MPa. For this reason, the preover boost pressure can be set to 6.0 MPa.
- the third temperature T3 when the third temperature T3 is set to 50 ° C., when the second pressure P2 is increased from 0 regardless of the magnitude of the fourth pressure P4, the above equation (4) is satisfied.
- the second pressure P2 at which the total enthalpy difference ⁇ htotal was first maximized was calculated as 6.5 MPa.
- the preover boost pressure can be set to 6.5 MPa.
- FIG. 12 and FIG. 13 show an example in which the preover boost pressure is specified as a pressure lower than the critical pressure, the present invention is not limited to this.
- the second pressure P2 when the second pressure P2 is increased from 0, the second pressure P2 at which the total enthalpy difference ⁇ htotal of the above equation (4) first maximizes is specified as a pressure equal to or higher than the critical pressure. There may be cases. For this reason, when specifying a preover boost pressure using the above equation (4), the preover boost pressure may be specified as a pressure higher than the critical pressure.
- the specification of the pre-over boost pressure using the above formulas (1), (3), and (4) is a process (third point C3) that is the optimum condition for converting the cold energy into electric power with the highest efficiency in the cold utilization process.
- the expansion turbine inlet pressure is specified.
- the primary generator of the primary turbine generator 18 and the secondary generator of the secondary turbine generator 20 are different from each other.
- the present invention is not limited to this.
- the generators of the primary and secondary turbine generators 18 and 20 may be a common generator.
- the primary power generation apparatus uses a Rankine cycle, but is not limited to this, and may use a steam power cycle other than the Rankine cycle.
- the second pressure P2 that maximizes the total enthalpy difference ⁇ htotal is set to the pre-over boost pressure, but is not limited thereto.
- the second pressure P2 at which the total enthalpy difference ⁇ htotal is greater than 0 and less than the maximum value may be set as the preover boost pressure.
- the low-temperature liquefied gas stored in the storage tank is not limited to liquefied natural gas, and may be, for example, liquefied petroleum gas, liquefied chlorofluorocarbon, or liquefied hydrogen.
- LPG was used as the working fluid (intermediate medium) of the Rankine cycle, and the efficiency coefficient ⁇ was set to 0.136.
- the existing cold power generation system will stop operation when commercial power from outside such as an electric power company is lost. For this reason, the existing cold power generation system cannot generate power even when it is a power generation system at the time of a power failure of a commercial power source.
- the power source for control, seawater, and liquefied natural gas (specifically, the secondary pump) are used for the thermal power generation system (LSG) using the power of another emergency generator.
- LSG is preferentially activated by supplying liquefied natural gas from 12).
- the electric power generated by the LSG can be fed to the other manufacturing plant on the premises in a system linkage with the premises electric power, and the other manufacturing plants can be operated in order.
- the LSG functions as an “emergency power supply device” in the event of an external commercial power supply loss or a power outage, and functions as a base load power supply for premises power during normal times.
- Liquefied natural gas is produced using a large amount of electricity in the natural gas liquefaction process in foreign production areas, and then transported by tankers.
- the LNG transport tanker transports “liquefied natural gas” + “liquefied power”. That is, LSG is a system that efficiently recovers and uses cooling power (low-cost power) used in natural gas production areas as power (high-cost power) in natural gas consumption areas. For this reason, the LNG transport tanker has the value of “liquefied natural gas carrier” and “electric power carrier”, and purchasing liquefied natural gas is the same as purchasing liquefied natural gas and local power.
- the LNG transport tanker is divided into “liquefied natural gas carrier” and “electric power carrier” (the power value in the upstream (production area) and downstream (consumption area) of LNG.
- electric power carrier the power value in the upstream (production area) and downstream (consumption area) of LNG.
- liquefied natural gas is stored in storage tanks.
- LSG that efficiently extracts the cold energy of liquefied natural gas creates the value of “liquefied natural gas storage” and “electric power storage” in the storage tank.
- the liquefied natural gas storage tank as an electric power storage, contributes to the leveling of peak power consumption during the day and night and the improvement of the unit consumption of day and night power. Therefore, by configuring an energy system including a storage tank and an LSG, a business model is provided in which storage tanks storing liquefied natural gas are designated as “liquefied natural gas storage tanks” and “electric power storage stations”. be able to.
- Businesses importing liquefied natural gas will use LSG's cold energy to generate power efficiently at the liquefied natural gas vaporization base, and self-consigned (outside the power generation site due to the revision of the Electric Business Law system) Power consumption), the total amount of power used by the facility in all areas of the operator can be self-sufficient. For this reason, a business model of “zero emission business” can be provided.
- an energy system that includes LSG and liquefied natural gas liquefaction equipment, boil-off gas (BOG), which has been vaporized by natural heat input in the storage tank, is liquefied with nighttime power during the daytime. If the power is generated by LSG and the electric power is taken out, it is possible to equalize the amount of electric power used day and night. Therefore, it is possible to provide a business model of “leveling daytime and nighttime peak power”.
- BOG boil-off gas
- SYMBOLS 10 Storage tank, 14 ... Tertiary pump (pressure
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Abstract
Description
上式(1)において、Δh1を第1エンタルピ差と称し、Δh2を第2エンタルピ差と称し、Δh3を第3エンタルピ差と称し、Δhtotalを合計エンタルピ差と称すこととする。各エンタルピ差Δh1,Δh2,Δh3を定義するために、図2に示すモリエル線図における冷熱利用プロセス(冷熱発電プロセス)の各動作点についてまず説明する。
冷熱エネルギ=温度エネルギ+圧力エネルギ … (2)
と変換される。
・モル%(Mole percent)
メタン(CH4)=92%、エタン(C2H6)=4%、プロパン(C3H8)=3%、ブタン(C4H10)=1%
・重量%(Mass percent)
メタン=82.61%、エタン=6.7321%、プロパン=7.4043%、ブタン=3.2531%
・Molor mass
17.866(kg/kmol)
本実施形態では、上記組成の天然ガスの物性値を、アメリカ国立標準技術研究所(NIST)製の冷媒熱物性データベースソフトウェアであるREFPROP(Version9.1)を用いて計算した。その計算結果を以下に示す。
・臨界点A1(Critical point)
215.85(K)、6.8362(MPa)、206.87(kg/m^3)
・クリコンデンバール(Cricondenbar)
231.4(K)、7.6316(MPa)、141.58(kg/m^3)
・クリコンデンサーム(Cricondentherm)
247.35(K)、4.8965(MPa)、54.708(kg/m^3)
図3に、第1点C1から第2点C2の昇圧プロセス(等エントロピ変化)における天然ガスの各パラメータを、REFPROPを用いて計算した例を示す。
上式(3)は、気化プロセスにおける温度エクセルギの利用について、熱力学第2法則の効率(カルノー効率)の制約を課した式である。気化プロセスの全エンタルピ差を利用して、温度エクセルギを仕事に変換できるシステムを想定している。以下、上式(3)に基づくプレオーバーブースト圧力の特定手法について説明する。
α=1-T2/T3
=1-(-162+273.15)/(20+273.15)=0.621
なお、第1点C1から第2点C2までにおける等エントロピ変化において、液化天然ガスの温度が微小ではあるが上昇する。このため、第2圧力P2の大小に応じて第2温度T2が変化し、効率係数αが変化する。ただし本実施形態では、計算の簡単化のため、効率係数αの算出において、第1点C1から第2点C2までにおける液化天然ガスの温度変化が無いものとした。
この場合、効率係数αは、第2点C2における第2温度T2とA点CAにおけるガス温度とのそれぞれによって定まるカルノーサイクルの理論熱効率以下の値であってかつ0よりも大きい値として定義される。1次発電装置のランキンサイクルの作動流体を例えばLPG(プロパン)とする場合、A点CAにおける温度を例えば-44℃に設定する。そして、カルノーサイクルの理論熱効率は、第2点C2における第2温度T2(=-162℃)と、A点CAにおける温度TA(=-44℃)とを用いて以下のように計算できる。
α=1-T2/TA
=1-(-162+273.15)/(-44+273.15)=0.515
図12に、第3温度T3が20℃の場合における先の図4の第1,第3エンタルピ差Δh1,Δh3、及び第2エンタルピ差Δh2rankを上式(4)に代入して算出した合計エンタルピ差Δhtotalと、第2圧力P2との関係を示す。また、図13に、第3温度T3が50℃の場合における先の図6の第1,第3エンタルピ差Δh1,Δh3、及び第2エンタルピ差Δh2rankを上式(4)に代入して算出した合計エンタルピ差Δhtotalと、第2圧力P2との関係を示す。なお、図12及び図13のそれぞれにおける効率係数αを0.515とした。
Claims (15)
- 貯蔵タンクに貯蔵された低温の液化ガスを所定圧力まで液状態のまま昇圧する昇圧ポンプと、
前記昇圧ポンプによって昇圧された前記液化ガスと所定の冷熱交換対象とを熱交換させることにより、前記冷熱交換対象を冷却させるとともに前記液化ガスを気化させる気化器を有する1次装置と、
前記気化器において気化された前記液化ガスである気化ガスによって駆動される2次タービンを有する2次装置と、を備え、
前記貯蔵タンクの貯蔵対象となるガスのモリエル線図上において、前記貯蔵タンクに貯蔵された状態の前記ガスの圧力及び温度を規定する点をプロセス開始点(C1)と定義し、
前記モリエル線図上において、前記気化器の入口側における前記ガスの前記所定圧力及び温度を規定する点をプレオーバーブースト点(C2)と定義し、
前記モリエル線図上において、前記2次タービンの入口側における前記ガスの圧力及び温度を規定する点であるタービン入口点(C3)、又は前記気化器の出口側における前記ガスの圧力及び温度を規定する点(CA)のいずれかを中間点と定義し、
前記モリエル線図上において、前記2次タービンの出口側における前記ガスの圧力及び温度を規定する点をタービン出口点(C4)と定義し、
前記プレオーバーブースト点におけるエンタルピから前記プロセス開始点におけるエンタルピを減算した値を第1エンタルピ差(Δh1)として定義し、
前記中間点におけるエンタルピから前記プレオーバーブースト点におけるエンタルピを減算した値を第2エンタルピ差(Δh2;Δh2rank)として定義し、
前記2次タービンの入口側における前記ガスの圧力及び温度を規定する点であるタービン入口点(C3)における状態から前記タービン出口点における状態となるまでに前記2次タービンによってなされる仕事を第3エンタルピ差(Δh3)として定義し、
前記第2エンタルピ差及び前記第3エンタルピ差の加算値から前記第1エンタルピ差を減算した値、又は前記プレオーバーブースト点及び前記中間点のそれぞれの温度によって定まるカルノーサイクルの理論熱効率以下の値であって0よりも大きい値である効率係数を前記第2エンタルピ差に乗算した値と前記第3エンタルピ差との加算値から、前記第1エンタルピ差を減算した値のいずれかを合計エンタルピ差(Δhtotal)として定義し、
前記所定圧力は、前記合計エンタルピ差に基づいて設定されていることを特徴とする冷熱利用システム。 - 前記合計エンタルピ差は、前記第2エンタルピ差及び前記第3エンタルピ差の加算値から前記第1エンタルピ差を減算した値として定義されることを特徴とする請求項1に記載の冷熱利用システム。
- 前記気化器は、蒸気動力サイクルを循環する前記冷熱交換対象としての作動流体と前記昇圧ポンプによって昇圧された前記液化ガスとを熱交換させることにより、前記作動流体を凝縮させるとともに前記液化ガスを気化させるものであり、
前記気化器から流出した気化ガスを加熱して昇温させる加熱器をさらに備え、
前記1次装置は、前記気化器に加えて、前記気化器において凝縮された作動流体を蒸発させる蒸発器、及び前記蒸発器において蒸発された作動流体によって駆動される1次タービンを有し、前記1次タービンが駆動されることにより発電する発電装置であり、
前記2次装置は、前記加熱器によって昇温された気化ガスで前記2次タービンが駆動されることにより発電する直接膨張方式の発電装置であることを特徴とする請求項1に記載の冷熱利用システム。 - 前記蒸気動力サイクルは、ランキンサイクルであることを特徴とする請求項3に記載の冷熱利用システム。
- 前記合計エンタルピ差は、前記効率係数を前記第2エンタルピ差に乗算した値と前記第3エンタルピ差との加算値から、前記第1エンタルピ差を減算した値として定義されるものであることを特徴とする請求項3又は4に記載の冷熱利用システム。
- 前記所定圧力は、前記プレオーバーブースト点における前記ガスの圧力を0から上昇させていく場合に前記合計エンタルピ差が最初に極大となる圧力に設定されていることを特徴とする請求項1ないし5のいずれか1項に記載の冷熱利用システム。
- 前記第3エンタルピ差は、前記モリエル線図上において前記ガスの状態が気液混合相に入らないように、前記2次タービンの入口側における前記ガスの圧力及び温度を規定する点であるタービン入口点(C3)における状態から前記タービン出口点における状態となるまでに前記2次タービンによってなされる仕事として定義されることを特徴とする請求項1ないし6のいずれか1項に記載の冷熱利用システム。
- 前記所定圧力は、前記液化ガスの臨界圧力以上の圧力に設定されており、
前記気化器は、前記昇圧ポンプによって昇圧された前記液化ガスと前記冷熱交換対象とを、前記液化ガスの圧力を前記臨界圧力以上に維持したまま熱交換させることにより、前記冷熱交換対象を冷却させるとともに前記液化ガスを気化させるものであることを特徴とする請求項1ないし7のいずれか1項に記載の冷熱利用システム。 - 貯蔵タンクに貯蔵された低温の液化ガスを、その臨界圧力以上の所定圧力まで液状態のまま昇圧する昇圧ポンプと、
前記昇圧ポンプによって昇圧された前記液化ガスと所定の冷熱交換対象とを、前記液化ガスの圧力を前記臨界圧力以上に維持したまま熱交換させることにより、前記冷熱交換対象を冷却させるとともに前記液化ガスを気化させる気化器を有する1次装置と、
前記気化器において気化された前記液化ガスである気化ガスによって駆動される2次タービンを有する2次装置と、を備えることを特徴とする冷熱利用システム。 - 前記液化ガスは、液化天然ガスであることを特徴とする請求項1ないし9のいずれか1項に記載の冷熱利用システム。
- 前記液化ガスは、2種以上の組成からなる混合ガスであり、
前記所定圧力は、前記液化ガスのクリコンデンバール以上の圧力に設定されており、
前記気化器は、前記液化ガスの圧力を前記クリコンデンバール以上に維持したまま前記液化ガスと前記冷熱交換対象とを熱交換させるものであることを特徴とする請求項1ないし10のいずれか1項に記載の冷熱利用システム。 - 液化ガスを輸送する輸送タンカーと、請求項1ないし11のいずれか1項に記載の冷熱利用システムと、を備え、
前記冷熱利用システムは、液化ガスの冷熱によって発電する冷熱発電システムとして構成されていることを特徴とするエネルギシステム。 - 液化ガスを貯蔵する貯蔵タンクと、請求項1ないし11のいずれか1項に記載の冷熱利用システムと、を備え、
前記冷熱利用システムは、液化ガスの冷熱によって発電する冷熱発電システムとして構成されていることを特徴とするエネルギシステム。 - 請求項1ないし11のいずれか1項に記載の冷熱利用システムの利用方法であって、
前記冷熱利用システムは、液化ガスの冷熱によって発電する冷熱発電システムとして構成されており、
前記冷熱利用システムを稼働させている事業者の設備の電力供給源として、前記冷熱利用システムを利用することを特徴とする冷熱利用システムの利用方法。 - 液化ガスを貯蔵する貯蔵タンクと、請求項1ないし11のいずれか1項に記載の冷熱利用システムと、を備え、
前記冷熱利用システムは、前記貯蔵タンクに貯蔵された液化ガスの冷熱によって発電する冷熱発電システムとして構成されており、
前記貯蔵タンク内で液化ガスが気化したボイルオフガスを夜間電力で液化するとともに前記貯蔵タンクに液化ガスとして再度貯蔵させる設備をさらに備えることを特徴とするエネルギシステム。
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