The present invention applies to the energy field, in particular for improving the energy efficiency of plants for regasifying liquefied natural gas.
Technologies are known for regasifying liquefied gases, such as liquefied natural gas (LNG), for example.
The liquefied natural gas is a mixture of natural gas mainly consisting of methane and, to a lesser extent, of other light hydrocarbons, such as ethane, propane, iso-butane, n-butane, pentane, and nitrogen, which is converted from the gaseous state, in which it is at ambient temperature, to the liquid state, at about −160° C., to allow the transport thereof.
Liquefaction plants are located close to natural gas generating sites, while regasifying plants (or “regasifying terminals”) are located close to the users.
Most of the plants (about 85%) is located onshore, while the remaining part (about 15%) is located offshore on platforms or ships.
It is common for each regasifying plant to comprise several regasifying lines in order to meet the liquefied natural gas load or requirements, as well as for reasons of flexibility or technical need (for example, for line maintenance).
Usually, the regasifying technologies involve liquefied natural gas stored in tanks at atmospheric pressure at the temperature of −160° C. and comprise the steps of compressing the fluid up to about 70 to 80 bar and vaporization and superheating up to about 3° C.
The thermal input required for regasifying 139 t/h is about 27 MWt, while the electric one is about 2.25 MWe (4.85 MWe if the other auxiliary loads of the plant are considered; maximum 20 MWe electric load of the plant on 4 regasifying lines in operation).
The most used regasifying technologies, individually or combined with each other, comprise the Open Rack Vaporizer (ORV) technology, employed in about 70% of the regasifying terminals (in the world), and the Submerged Combustion Vaporizer (SCV).
Other technologies employ the Intermediate Fluid Vaporizer (IFV) or the Ambient Air Vaporizer (AAV).
Open Rack Vaporizer (ORV)
This technology provides for the natural gas in the liquid state (about 70 to 80 bar and at the temperature of −160° C.) to be flown from the bottom upwards in aluminum pipes placed side-by-side to form panels; the vaporization progressively occurs as the fluid proceeds.
The heat carrier is seawater which flowing from the top downwards over the outer surface of the pipes, provides the heat required for the vaporization by difference in temperature.
In particular, the heat exchange is optimized by the design of the profile and the surface roughness of the pipes, which create a homogenous distribution of the thin seawater film over the panel.
Submerged Combustion Vaporizer (SCV)
Such a technology utilizes a demineralized water bath heated by an immersed flame burner as heat carrier; in particular, the Fuel Gas (FG) is burned in the combustion section and the fumes generated pass through a coil of perforated pipes from which the combusted gas bubbles passes outside, which combusted gas bubbles heat the water bath by also yielding the condensation heat.
The liquefied natural gas (LNG) vaporizes in another coil of stainless steel pipes immersed in the same demineralized and heated water bath.
The same water of the bath is kept in circulation in order to ensure a homogenous temperature distribution.
The exhausted fumes instead are discharged from the exhaust gas stack of the SCVs.
Organic Rankine Cycle
The Organic Fluid Rankine Cycles (ORCs) are widely used in the geothermal field and for biomass applications or for Waste Heat Recovery from industrial processes.
Such cycles provide the possibility of selecting the operating fluid from a broad variety of candidate fluids and allows efficient thermodynamic cycles to be obtained, also for low temperatures of the heat source and for little availability of thermal energy.
Moreover, the selection of a low boiling fluid allows a condensing cycle at cryogenic temperatures to be achieved without problems of freezing or ultra-high vacuum degrees.
Submerged Combustion Vaporizer (SCV) and Open Rack Vaporizer (ORV)
The (SCV) technology results in a consumption of fuel gas equal to about 1.5% of the processed gas and generates carbon dioxide which lowers the pH of the water bath, requiring treatments with caustic soda and thus causing an emission of CO2 into the atmosphere of about 50,000 t/year in order to regasify 139 t/h of LNG.
With regard instead to the Open Rack Vaporizer (ORV), such a technology may partially cause the freezing of the seawater in the outer part of the pipes, especially in the sections in which the LNG is colder; moreover: i) it may be utilized in the geographical regions and/or in the seasons in which the temperature of the seawater is at least 5-9° C., mainly represented by the subtropical areas, ii) the seawater is to be processed beforehand to eliminate or reduce the content of the heavy metals which could corrode the zinc covering of the pipes, iii) it results in a consumption of electrical energy for operating the pumps for the seawater which is to exceed a geodetic difference of level equal to the development in height of the ORVs with additional consumptions of about 1 MWe per regasifying line with respect to the SCV technology (requiring a total power of about 20 MWe for a plant with four regasifying lines of 139 t/h each), iv) it results in an environmental impact in returning the colder and processed seawater, v) lastly, the technology is rather complex and available at a limited number of suppliers and of size.
A transcritical power generating cycle which employs CO2 is depicted in
Such a cycle does not take into consideration the employment of the LNG frigories, neither directly nor by means of intermediate fluids, with the following limitations:
In the case of an not-recovered supercritical/transcritical CO2 topping cycle, the recuperator which lowers the temperature of the CO2 to the benefit of the efficiency of the cycle itself is not output from the CO2 turbine; therefore, the CO2 still at a relatively high temperature is the thermal input for the ORC bottoming cycle.
Using a not-recovered CO2 cycle thus means extracting mechanical energy in a poorly efficient manner from a system which would potentially be more efficient with a recuperator or recompressor. The thermal energy not used in the CO2 cycle is sent to the ORC bottoming cycle, which would operate with a significant difference in temperature and therefore, an increased pressure ratio, making difficult the design of turbomachinery, to the benefit of a moderate increase in efficiency with respect to a CO2 system.
Therefore, the conventional and/or already known technologies do not generally allow the electrical energy required for the plant to be generated and result in the loss of a large quantity of energy in the form of frigories.
The inventors of the present patent application have surprisingly found that there may be designed a power generating cycle employing an operating fluid, which may be employed for regasifying LNG, thus generating sufficient electrical energy to operate the plant.
Therefore, a first object of the invention is represented by a process for regasifying a fluid and for generating electrical energy.
In a second object it is described a regasifying line of the liquefied gas which allows generating electrical energy by utilizing the process of the invention, and a plant comprising such a line.
The present invention is particularly described in relation to regasifying liquefied natural gas (LNG), but it is equally applicable for regasifying or vaporizing other liquefied fluids stored at low temperatures (lower than about 0° C.) or at cryogenic temperatures (lower than −45° C.)
For example, the present invention is applied for regasifying a liquefied gas selected from the group which comprises, for example: air, nitrogen, commercially available hydrocarbon compounds such as alkanes, including for example propane and butane, or alkenes, including for example ethylene and propylene.
The terms “evaporation” and “vaporization”, which are applicable to LNG, are to be intended as synonyms in the following description.
Moreover, “liquefied natural gas”, later also referred to as “liquefied gas”, in the present description means a liquid obtained from natural gas after suitable refining and dehydrating processes and next cooling and condensation steps.
More generally, “liquefied gas” in the present description means a fluid having a mainly liquid component.
Moreover, the term “low temperature heat source” in the present description means for example: ambient air, seawater, low temperature solar thermal, exhaust heat of a low temperature thermodynamic cycle, low temperature process and/or machinery heat recovery.
A low temperature source generally operates at temperatures, which are lower than 180° C., preferably lower than 120° C.
The term “high temperature heat source” instead means for example: high temperature thermal solar, exhaust heat of a high temperature thermodynamic cycle, exhaust gas of a gas turbine or internal combustion engine, high temperature process and/or machinery heat recovery.
A high temperature source generally operates at temperatures, which are higher than 180° C., preferably higher than 300° C., and even more preferably higher than 400° C. and beyond.
For the purposes of the present invention, it may be provided that the same low or high temperature heat source feeds several heating systems.
In the continuation of the description, the term “seawater” refers not only to seawater conveniently processed to remove sediments and conveniently pumped (for example at about 2 bar), but more generally, environmental water obtained from rivers, canals, wells, natural basins such as lakes, etc. and artificial basins.
For the purposes of the present invention, the operating fluid is CO2.
For the purposes of the present invention, an intermediate operating fluid is a fluid capable of carrying out a heat transfer from one cycle to another.
Such an intermediate operating fluid may perform for example a heat transfer from a first power cycle (to which reference may be made as a topping cycle) and to a second power cycle (to which reference may be made as a bottoming cycle).
In one aspect of the invention, the bottoming cycle is a power cycle equal to the topping cycle.
In a preferred aspect, the intermediate operating fluid is different from the operating fluid of the topping cycle.
For the purposes of the present invention, an operating fluid is involved which is different from CO2 and preferably is a gas or a gas mixture selected from the group comprising: hydrocarbons, nitrogen, CO2 and coolants.
According to a first object, the present invention describes a process for regasifying a fluid to be regasified and for generating electrical energy.
As described above, such a fluid to be regasified preferably is LNG.
In a particular aspect of the present invention, the process comprises the employment of an operating fluid, which preferably is CO2.
More in detail, the process comprises subjecting an operating fluid to the steps of:
1) pumping,
2) heating in a recuperator, thus obtaining a heated flow,
3) heating through a high temperature source, thus obtaining a further heated flow,
4) expanding in a turbine, with generation of electrical energy (through a generator), thus obtaining an expanded flow,
5) cooling in a recuperator, thus obtaining a cooled flow,
6) condensing said operating fluid flow.
For the purposes of the present invention, step 1) comprises a low pressure pumping sub-step 1a) and a high pressure pumping step 1b).
Step 1a) increases the pressure up to about 30 to 60 bar.
Step 1b) increases the pressure beyond about 150 bar.
More specifically, after the low pressure pumping step 1a), a portion of the flow of said operating fluid is subjected to a recompression step.
The recompression increases the pressure up to about 150 bar.
In a preferred aspect, said flow is subjected to a vaporization step I) prior to recompression.
With regards to step 2), said step comprises a low temperature heat recovery step 2a) (LTR) and a high temperature heat recovery step 2b) (HTR).
In particular, step 2a) increases the temperature up to about 200° C.
The flow of the operating fluid obtained after the recompression is then combined with the flow of the operating fluid obtained from step 2a) to be subjected to step 2b).
According to the present invention, the operating fluid is CO2 and such an expansion step 4) is therefore a transcritical expansion step.
For the purposes of the present invention, step 5) is carried out in the same recuperator as step 2); indeed, the heat exchange of step 5) is carried out with the flow of steps 2b) (high temperature recovery or step 5a)) and 2a) (low temperature recovery or step 5b), respectively, and allows a cooled flow to be obtained.
As described above, the operating fluid may be CO2; alternatively, an operating fluid may be employed mainly consisting of CO2 with the addition of hydrocarbon/additive mixtures, which allow this fluid to be liquefied at higher temperatures than the ambient temperature or to the one of the available cold fluid.
According to a first aspect of the invention schematized in
In one aspect of the present invention, the above-described vaporization step I) may be carried out by employing a low temperature heat source, as defined above.
In another aspect of the present invention, the heating step 3) may be carried out by employing a high temperature heat source, as defined above.
According to another aspect of the present invention, the fluid to be regasified may be subjected to a superheating step after step 6).
In particular, said superheating step may be carried out by employing a low temperature heat source.
For the purposes of the present invention, the flow of operating fluid employed in steps from 1) to 6) of the described process is the flow of operating fluid obtained after the condensation step 6), thereby configuring a cycle.
According to a second embodiment of the present invention depicted in
In a preferred aspect of the present invention, the operating fluid is CO2 and therefore such a further expansion step is a subcritical expansion step.
According to an alternative embodiment of the present invention depicted in
More specifically, such an indirect exchange occurs by means of an intermediate operating fluid, as described above.
Such an intermediate operating fluid circulates within a cycle, referred to as a bottoming cycle.
More in detail, said bottoming cycle comprises a first exchanger COND1 (which corresponds to the condenser of step 6) and which is the condenser of the topping cycle), inside of which the heat exchange is carried out between the operating fluid and said intermediate operating fluid which is thus heated, and a second exchanger COND2, inside of which the heat exchange is carried out between the intermediate operating fluid and the fluid to be regasified, to which heat is yielded.
For the purposes of the present invention, the vaporization step I) carried out prior to recompression, the heating step 3) and the possible superheating step of the fluid to be regasified are carried out by employing heat sources as described above.
In one aspect of the present invention depicted for example in
Such a configuration, which may equally be applied also in the presence of a bottoming cycle
According to a further aspect of the present invention not depicted in the drawings, the turbine may actuate the low pressure pump and/or the high pressure pump.
For the purposes of the present invention, the described process may further comprise a step of regulating the circulating mass flow of CO2 in the cycle, wherein the CO2 is kept at the liquid state (also by virtue of the frigories provided by the cold source, and pressurized).
For this purpose, the plant may comprise a CO2 storage tank.
Such adjustment advantageously allows the power of the cycle to be regulated.
According to a second object of the present invention, there is described a regasifying line for a fluid, preferably the liquefied natural gas (LNG) which allows generating electrical energy by means of the above-described process.
The term “regasifying line” means that independent and replicable portion of the plant that includes the structures, the equipment, the machinery and the systems for regasifying a given flow of the liquefied natural gas (LNG).
In particular, such structures, equipment, machinery and systems originate from the tank (TANK) in which the LNG is stored, and comprise cryogenic pumps, possibly low and high pressure pumps and a BOG compressor, which may be common to several regasifying lines, and a regasification section, and end with the regasified LNG introduction point into the distribution network of the gas itself.
For the purposes of the present invention, the regasification section is the condenser wherein step 6) of condensing the operating fluid and regasifying the fluid to be regasified occurs, according to the above-described process.
Alternatively, a regasifying line of the present invention may be provided in energy bypass configuration with respect to a traditional technology of an existing plant.
As shown in
According to an alternative embodiment of the present invention, the power cycle described may be integrated with a conventional technology of SCV type. Here, a coil containing condensing CO2 or a suitable fluid (such as, for example water-glycol) which exchanges heat with the condensing CO2 heats the vaporization bath.
The layouts proposed may also be applied for making plants for regasifying technical gas (such as, for example hydrogen, air, nitrogen or other gas) or plants with low or cryogenic temperature fluid storages, also for cryogenic depots or storages.
When an export of electrical energy is not provided, to balance out the electric and heat loads, the power cycle may operate on a fraction of the LNG, regasifying the remaining fraction of LNG, with other systems and/or employing the surplus of electric power to feed air heating technologies.
In an alternative configuration, the CO2 fraction which is not employed for regasifying LNG may be employed for achieving a cooling/liquefaction of the air by utilizing also a part of the electric power generated by the cycle itself, if required; thereby, in addition to obtaining a liquid air storage, nitrogen and oxygen may be obtained, and the latter may be employed to achieve a CO2 cycle with internal oxy-combustion technologies.
The values indicated in the following section refer to a reference regasifying plant by way of explanation, but are in any case valid if considered as specific/unitary value.
Moreover, the results obtained in terms of extractible net electric power and thermodynamic efficiency of the cycle refer to a pressure of 100 to 250 or 150 to 350 bar and beyond A, and at a temperature of about 350° C. to 550° C. or 450° C. to 650° C., up to 700° C. and beyond, at the transcritical expansion turbine input, where applicable.
The diagram in
The variation with respect to the diagram of the background art in
Then, it is not separated but is entirely sent to the condenser (COND 1), condensing at a lower pressure with respect to the diagram in
Indeed, the fluid is sent to a low pressure pump (LP-P) where it is pumped at a pressure between 30 and 60 bar (7), in any case corresponding to the evaporation temperature in (11). The fluid is output from the low pressure pump divided into two flows. The first flow (14) is sent into a high pressure pump (HP-P) and is pumped at a pressure higher than 150 bar (8), then it is sent to the heat exchanger (LTR) where it is preheated at a maximum temperature of about 200° C. (9). The second flow (13) is vaporized by the ambient heat to a variable ambient temperature between 0° C. and 30° C. through an air cooler (AMB VAP or LTR2) (11) and then is sent to the recompressor (R-COMPR) to be compressed at a higher pressure than 150 bar (12). This flow output from the recompressor is combined with the one (9) from the first heat exchanger (LTR) and is sent to the second heat exchanger (HTR) (10) to be further superheated (1).
The main results are: a net electric power up to 21.4 MWe, thermodynamic performance up to 62.2% (not considering the ambient heat in AMB VAP/LTR2), employing a total circulating CO2 of 294.6 t/h.
123.61 t/h of LNG are drawn at the temperature of −156.6° C. and at a pressure of 90.5 bar A (100). Then, the LNG receives heat in COND 1 (24.34 MWt), reaching the temperature of 2.5° C. (101).
If the employment of a seawater circuit is provided (optional for the vaporization of the CO2, not depicted in the drawings), an (optional) seawater circuit may be integrated in the CO2 cycle to provide the heat duty required at AMB VAP to vaporize the CO2.
With reference to the above-described case, 1828.44 t/h of seawater at the temperature of 30° C. and at atmospheric pressure are drawn at the seawater intake and pumped at the pressure of about 2 bar A by means of a pump. The flow is then fed to the CO2 AMB VAP (10.61 MWt) vaporizer, where it is cooled by 5° C. and discharged into the sea, thus allowing the vaporization of the CO2 at a pressure of 45.01 bar and a corresponding temperature of 10° C. (11) on the other side of the exchanger AMB VAP.
The main results in terms of net electric power and thermodynamic performance are entirely similar to those obtained in the above-described case, less the power required for pumping the seawater.
The same reference diagram in
The circuit is the same, but the LNG is not entirely regasified, i.e. up to a temperature of 2.5° C., by means of the condensation of the power cycle. Indeed, the remaining portion is regasified through an ambient means, which may be seawater. Moreover, it is employed for the vaporization of the CO2 in AMB VAP (also described in the option indicated in the above-indicated case).
With respect to the diagram in
The output temperature of the natural gas (LNG regasification) is lower given that it is heated with the CO2 cycle through the same condenser (COND 1) with a variable temperature reached between −55° C. and 0° C. (101). Therefore, a further superheating fluid is required to heat the natural gas at the required temperature, included between 0 and 10° C. (in the particular case, of 2.5° C.). For this purpose, the natural gas is sent into an ambient air cooler or into an optional seawater circuit (102).
With respect to the above-described circuit (diagram 3A without the dotted section), the LNG is not entirely vaporized up to the temperature of 2.5° C. through the heat exchange with the CO2 in COND1. The following description is consistent with the balance indicated above.
123.61 t/h of LNG are drawn at the temperature of −156.6° C. and at a pressure of 90.5 bar A (100). Then the LNG receives heat (17.4 MWt) if, as indicated above, the pressure CO2 circuit side to the flow (6) is equal to 8.318 bar in COND1 up to reaching a temperature of −46° C. (101). The remaining part of the vaporization, which is dependent on the preceding heat exchange in COND1, is completed in the heater SH where the LNG receives heat from the seawater circulating in a dedicated circuit and reaches a temperature of 2.5° C. (102).
A seawater circuit is installed to provide, downstream of COND1, the remaining heat required for the vaporization of the LNG up to 2.5° C. Moreover, it may (optionally) be integrated in the CO2 cycle to provide the heat duty required to vaporize the CO2 in AMB VAP and it requires being integrated.
With reference to the actual above-described case, 2681.39 t/h of seawater at the temperature of 30° C. and at an atmospheric pressure are drawn at the seawater intake and pumped at the pressure of about 2 bar A by means of a pump. Of this flow, a part, i.e. 1485.31 t/h, of seawater are (optionally) fed to the vaporizer AMB VAP (8.62 MWt) where they are cooled by 5° C., thus allowing the vaporization of the CO2 at a pressure of 45.01 and a corresponding temperature of 10° C. (11) on the other side of the exchanger AMB VAP. The remaining flow, i.e. 1196.08 t/h of seawater, instead is fed to the heater SH (6.94 MWt) where it is cooled by 5° C., thus allowing the vaporization of the LNG from the temperature obtained at the output of COND1 up to reaching a temperature of 2.5° C., not obtained with the condenser COND1 alone. It therefore is mixed with the flow output from AMB VAP and is discharged into the sea at the temperature of 25° C.
Alternatively, as shown in diagram 2B, the cycle in
It is worth noting the reference diagram in
The diagram provides for the operating fluid at the output of the heat exchangers (HTR and LTR, where the fluid is desuperheated (5)) to be further expanded in SC-EXP (15) prior to being fed to COND1.
The advantages offered by the present invention are apparent to a person skilled in the art from the description above.
Considering the conventional regasification technologies, the main advantages of the solution appear to be:
Moreover, more in detail, the following was positively noted:
More specifically, with respect to the CO2 transcritical power generating cycles, the following advantages can be recognized:
With reference to the drawings in
With reference to the drawings in
Overall, the cascade power generating cycles may be combined so as to best utilize the features and constraints thereof to the advantage of regasifying the LNG, thus improving the employment of the frigories (vaporization curve). Although they have increased engineering complexity, they allow the overall plant efficiency to be improved.
In the case of a CO2 topping cycle and a bottoming cycle with fluid different from CO2 as described above:
Moreover, the CO2 topping cycle is a supercritical/transcritical cycle with recuperator and recompressor, therefore the energy available at high temperature is utilized well in a high efficiency topping cycle, instead designating the energy at lower temperatures (the one discharged from the top cycle) to the ORC bottoming cycle. The two cascade cycles (CO2 topping cycle and ORC bottoming cycle) are optimized with the heat inputs in the temperature ranges appropriate thereto, with benefits to the overall efficiency and simplification in designing the turbomachinery.
All the embodiments of the invention may operate in configuration both of energy bypass at a conventional regasifying technology for an existing plant (as shown in
Number | Date | Country | Kind |
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102019000004727 | Mar 2019 | IT | national |
Filing Document | Filing Date | Country | Kind |
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PCT/IB2020/052455 | 3/18/2020 | WO | 00 |