Method and System for Ultra-Low Emissions of Natural Gas Storage and Redeployment

Information

  • Patent Application
  • 20250146744
  • Publication Number
    20250146744
  • Date Filed
    November 01, 2024
    a year ago
  • Date Published
    May 08, 2025
    7 months ago
Abstract
The disclosed subject matters include a system and method of storing and redeploying a gaseous fuel with low vapor emissions. An exemplary method includes a dehydration and liquefaction of a gaseous fuel, a pressurization storage and vaporization of the liquid fuel on demand. The method may further include an automation and monitoring.
Description
BACKGROUND

The present disclosure relates generally to energy conservation, and more particularly, to a liquefaction, storage, and redeployment of a gaseous fuel.


As natural gas came to be produced, long-distance transport and local distribution pipelines had an inherent, but limited, amount of buffer capacity for gaseous fuel storage. Typically, pipelines are not built to flow at peak demand, e.g., for cold climates, and it is more economical to build local storage capacity for generality. To increase the buffer supply in natural gas systems, especially at points away from production and closer to consumers, natural gas has been liquified to make it denser so that more can be stored for deployment at times of peak demand.


Typically, natural gas storage technology includes a process of liquefying natural gas, involving cooling and storing at near atmospheric pressure and cryogenic temperatures of around minus 162 degrees C. and minus 259- or 260-degrees F., where the natural gas can be converted into a liquid state in dense volume. The natural gas taken from the ground typically has components that must be removed from the gas before processing to prevent them from freezing and clogging the liquefied natural gas (short for LNG) production flow. Components that are often required to be removed before cryogenic chilling include water, carbon dioxide (CO2), compounds containing sulfur, benzene, other aromatic hydrocarbons, and other hydrocarbon components with a carbon number of six or greater, e.g., heavy hydrocarbons.


In a conventional LNG system, this gas treatment typically employs expensive and complicated processes and devices, requiring a significant capital investment. Furthermore, conventional LNG production and storage typically requires removal of CO2 to prevent the CO2 from solidifying and clogging the liquefaction equipment, which results in a stream emission enriched in O2 releasing into atmosphere. Removal of CO2 from the gaseous fuel by adsorption or distillation has been applied in the current LNG storage industries. However, the current art has to build CO2 treatment equipment into the LNG system. When CO2 is removed, e.g., by liquid amine processes or solid desiccants, the off stream is enriched CO2 and is typically released to the atmosphere. Further, since the concentrated CO2 may contain trace amounts of compounds that should be destroyed before release to the atmosphere, incinerators, also known as thermal oxidizers, consuming significant fossil fuels are employed to incinerate a stream that is mostly non-combustible CO2, often requiring temperatures in excess of one thousand degrees Fahrenheit. Significantly, the current technologies for LNG production and storage have not been reliable and efficient in achieving ultra-low carbon emissions, e.g., scope 1 and scope 2 GHG emissions.


Therefore, there is a need in the industry for an improved process or method for storing natural gas densely with minimum emissions, minimal equipment, minimal capital cost, minimum operational cost, minimum energy intensity, and/or minimum operational scope 1 and scope 2 GHGe intensity.





BRIEF DESCRIPTION OF THE DRAWINGS

The following figures are included to illustrate certain aspects of the present disclosure and should not be viewed as exclusive embodiments. The subject matter disclosed is capable of considerable modifications, alterations, combinations, and equivalents in form and function, without departing from the scope of this disclosure.



FIG. 1 is a schematic diagram of an exemplary system for natural gas storage and redeployment, according to one or more aspects of the present disclosure.



FIG. 2 illustrates a schematic diagram of an example process for natural gas storage and redeployment, according to one or more aspects of the present disclosure.



FIGS. 3a-3k illustrate schematic diagrams of an example process for natural gas storage and redeployment, according to one or more aspects of the present disclosure.



FIGS. 4a-4j illustrate schematic diagrams of an example process for natural gas storage and redeployment, according to one or more aspects of the present disclosure, showing one of many cryogenic liquefaction processes that can be deployed.



FIGS. 5a-5b illustrate a cryogenic liquefaction cooling process that can be deployed and incorporated into one or more aspects of the present disclosure.





DETAILED DESCRIPTION

Illustrative embodiments of the present invention are described in detail herein. In the interest of clarity, not all features of an actual implementation may be described in this specification. It will of course be appreciated that in the development of any such actual embodiment, numerous implementation-specific decisions may be made to achieve the specific implementation goals, which may vary from one implementation to another. Moreover, it will be appreciated that such a development effort might be complex and time consuming but would nevertheless be a routine undertaking for those of ordinary skill in the art having the benefit of the present disclosure.


Throughout this disclosure, a reference numeral followed by an alphabetical character refers to a specific instance of an element and the reference numeral alone refers to the element generically or collectively. Thus, as an example (not shown in the drawings), widget “1a” refers to an instance of a widget class, which may be referred to collectively as widgets “1” and any one of which may be referred to generically as a widget “1.” In the figures and the description, like numerals are intended to represent like elements.


The term “scope 1 emission(s)” or “scope 2 emission(s),” as used herein, refers to specific categories of greenhouse gas emissions (“GHGe”) in the environmental sustainability industry. “Scope 1 emissions,” as used herein, refers to direct greenhouse gas emissions that result from sources that are owned or controlled by an organization. Examples of Scope 1 emissions include emissions from on-site fuel combustion, such as those produced by company vehicles or the operation of a company-owned power plant. “Scope 2 emissions,” as used herein, refer to indirect greenhouse gas emissions that result from the generation of purchased or acquired electricity, heating, and cooling. They are indirect because the emissions occur at the facilities that generate the electricity or heat, not at the organization's own facilities. Scope 2 emissions include emissions associated with the energy a company buys from a utility.


The term “natural gas,” as used herein, refers to methane alone or blends of methane with other gases such as other light hydrocarbons (e.g., ethane) or heavier hydrocarbons (C3+) in any proportion that would exist as gas vapor at ambient temperature and pressure. A natural gas stream may also include minor amounts of non-hydrocarbon impurities (such as water, carbon dioxide, hydrogen sulfide, and nitrogen). This natural gas may have originated as a naturally occurring fluid stream extracted from the earth or as synthetically combined mixture of molecules created for the purposes of transport in or on some form of mobile platform (such as a ship, railcar, or truck trailer). For example, natural gas, which is predominantly methane, cannot be liquefied by simply increasing the pressure, as is the case with heavier hydrocarbons used for energy purposes. The critical temperature of methane is −82.5° C. (−116.5° F.). This means that methane can only be liquefied below that temperature regardless of the pressure applied. Since natural gas is a mixture of gases, it liquefies over a range of temperatures. The critical temperature of natural gas is between about −85° C. (−121° F.) and −62° C. (−80° F.).


The term “LNG”, as used herein, refers to “liquefied natural gas”. The term “CNG”, as used herein, refers to “compressed natural gas”, whether refrigerated or not. The term “PLNG,” as used herein refers to “pressurized liquid natural gas” or “pressurized natural gas liquid.” PLNG is deeply refrigerated but may not necessarily be stored at temperatures below the critical temperature of methane. Notably, PLNG can also be chilled, produced, and stored slightly cooler than −112° C. (−170° F.) so that it is subcooled and below its bubble point temperature at the selected pressure storage operating pressure. Since in this use case of natural gas storage there may be no need for fossil fuel for power, it is best to minimize vapor evolving from the chilled fluid expansion process, that is, to eliminate the production of “end flash gas”, though such can be selected to be done in other embodiments of this disclosure as long as the additional vapor is properly managed.


The term “impurities,” as used herein, refers to impurities that may exist in natural gas, which may be removed to ensure the quality and safety of the final product. The specific impurities may vary depending on the source of the natural gas, but common impurities that are typically removed during LNG production include: carbon dioxide, benzene, other aromatic hydrocarbons, and other heavy hydrocarbons.


To facilitate a better understanding of the present disclosure, the following examples of certain embodiments are given. In no way should the following examples be read to limit, or define, the scope of the disclosure. Embodiments described below with respect to one implementation are not intended to be limiting.


The present disclosure provides for systems and methods for storage and redeployment of natural gas with low emissions. Specifically, the present disclosure relates to a method and system for liquefaction, storage, and redeployment of a gaseous fuel (such as or similar to natural gas) with ultra-low vapor emissions and ultra-low scope 1 greenhouse gas emissions. Further, scope 2 emissions can be managed and reduced by procurement of electricity with lower scope 2 content, such as electricity produced via solar photovoltaic methods, wind turbines, nuclear means, hydrogen fuel of low GHGe intensity, other lower carbon-intensity methods of producing electricity, etc., as scope 2 emission can be primarily embedded in electricity imported to the facility. Additional, scope 1 and or scope 2 emissions can be managed lower via integration of lower carbon electricity production into the present disclosure, such as can happen if solar photovoltaic methods, wind turbines, nuclear means, hydrogen fuel of low GHGe intensity, other lower carbon-intensity methods of producing electricity, etc., were used to produce electricity within the natural gas storage facility. The disclosed systems and methods may further utilize by-products such as energy gas, e.g., ethane, propane and hydrogen, and may also incorporate carbon capture, utilization, and sequestration methods. The disclosed systems and methods may, in certain embodiments, dispatch the natural gas fuel on demand and conduct energy management integrated with an automation system comprising data acquisition and machine learning. In certain embodiments, the systems and methods of the present disclosure may provide a gaseous fuel storage and redeployment combined with an achievement of ultra-low emissions, especially scope 1 and scope 2 GHGe. The process is not limited to natural gas, but can be applicable to other gaseous fuels, e.g., hydrogen, ethane, propane ethane, or any other applicable gaseous fuels.


Advantages of the systems and methods of the present disclosure include, but are not limited to providing an improved process for storing natural gas densely with minimum gas treatment, minimum equipment, minimum capital cost, minimum operating cost, minimum energy intensity, minimum operational scope 1 and scope 2 GHGe intensity, while reducing to a practical minimum or near zero intentional release of gaseous emissions including flare and vents. Moreover, this system may include no venting of CO2 and no production of a stream with concentrated CO2. In addition, the system and methods of the present disclosure may use heat from ambient sources with electricity to vaporize the fuel back to a pressurized gaseous state using imported electricity or electricity not powered by fossil fuel combustion (avoiding releasing carbon dioxide from combustion into the atmosphere). Further, the system and methods of the present disclosure may include low leakage valves and flanges to reduce the fugitive emissions of components that are considered greenhouse gases, and pressure relieving devices with minimal through-devise gas flow such as rupture pins and burst disks either before or after pumping the fuel. Further, the systems and methods of the present disclosure may produce a PLNG product for storage and subsequent vaporization with concentrations of CO2 in the inlet that may result in the existence of solid CO2 in the pressurized storage tanks. Such may form in the expansion of the chilled stream upstream of the storage tank. In such a case, solid CO2 would be of higher density than the pressurized liquid natural gas and sink to the bottom of the tank, where it will remain until the tank is warmed and the gas in the tank sent to export.



FIG. 1 is a schematic diagram of an exemplary system 100 of the present disclosure for gaseous fuel storage and redeployment that may employ the principles of the present disclosure, according to one or more embodiments. As illustrated, the system 100 may include a dehydration unit 102, a liquefaction unit 104, a pressurized storage unit 106, a vaporization unit 108, and a plurality of reservoirs, valves, and pipelines. The system 100 further may be configured to integrated with a monitor unit 114 and an automation unit 110 for data processing on demand. In the dehydration unit 102, water removal may be implemented to remove any water or moisture from the incoming natural gas feedstock, which is significant to avoid clogging of the PLNG, storage, transportation (which could be done by mobile means to other sites of storage), and vaporization equipment. In another embodiment, trace water content may frost the inside of said components and, if operated in cyclic fashion, either with or without parallel equipment, said equipment can be rendered back to water free condition by a defrosting process. Furthermore, moisture removal can prevent corrosion in pipelines and storage tanks, as water can contribute to the corrosion process.


Through the dehydration unit 102, the dehydrated natural gas is delivered into the liquefaction unit 104, where natural gas is transformed from a gaseous state into a cryogenic liquid state for storage and transportation. Further, the PLNG obtained from the liquefaction unit 104 may be transported to other customers for their onsite storage. Such an embodiment may combine onsite storage for an anchor customer with a hub and spoke model connected to other customers who may have more modest onsite, reserve fuel demand. Typical processes in the liquefaction unit 104 may include gas impurities treatment (such as the removal of excess nitrogen, helium, etc.), gas compression, cooling and liquefaction.


In traditional production and storage of LNG, a CO2 removal unit may be located upstream of the dehydration unit 102 (e.g., if the gas impurity treatment involves water in a solution such as amine for CO2 removal) Additionally, the pressurized gas must typically be cooled to cryogenic temperatures, typically around −162 degrees Celsius (−260 degrees Fahrenheit) using a series of heat exchangers and refrigerants, enabling a transformation from the gas into a dense liquid, before being let down in pressure to about atmospheric.


In the present disclosure, the need to cool to −162 degrees Celsius is avoided by operating the liquefaction process and the storage at higher pressure than traditional process, for example more than 2 bar absolute. Raising the operating pressure may reduce the need for refrigeration power, sometime with a power saving of 20%, 40%, or more, depending on the inlet compositions, the operating pressure of liquefaction and storage, and the temperature of the ambient heat sink.


Further in the pressurized storage unit 106, the liquefied natural gas may not incur the freezing of impurities including carbon dioxide, depending on their concentration. In the methods and systems of the present disclosure, CO2 removal and concentration is not required. For example, even with one percent or more CO2 in the inlet, the CO2 may not form solids at some anticipated storage operating conditions of the present disclosure. Additionally, even if the CO2 content in the inlet is more than a few percent and is predicted to form solid CO2 at the liquefaction and storage operating conditions, the present disclosure includes means for managing solid CO2. Methods for predicting solid CO2 in cold methane mixtures are well known, so it can be discerned if providing such means per the current disclosure is prudent for one or more operating scenarios. Finally, in many gas transportation pipelines, the composition of the natural gas being transported changes over time. The present disclosure has means to time the sourcing of natural gas for storage to time of lower CO2 content, among other attributes. Therefore, the present disclosure for natural gas storage eliminates the need for adsorption or adsorption or other processes to removal and concentrate CO2.


One embodiment of the present disclosure is to take inlet gas and, if not already at a pressure of 450 psia, to compress to that pressure or greater, even up to 1400 psia or greater, and to chill it, and expand it to a pressure above 2 atmospheres for storage under pressure. Typical United State inter and intra state natural gas transmission lines can operate between about 450 and 1400 psia, though they can be based on their design operating below or above that pressure too, possibly even above 2160 psi.


The degree of dehydration for the inlet gas depends on the temperature of the PLNG product to be stored. Typically for processing temperatures significantly cooler than −40 degrees Celsius (−40 degrees Fahrenheit), dehydration units comprised of molecular sieve beds are used to remove water content down to the range of about one part per million or less. One or more beds are used for inlet gas dehydration while often one or more other beds are regenerated by hot gas to remove water that has been previously adsorbed in the cyclic operation of the beds, or being cooled by dehydrated, cooler gas. Alternatively, it may be possible to use some other type of solid desiccant or even some type of liquid glycol of ultra-high purity to dehydrate the inlet gas in an absorption process.


The amount of CO2 that can be in natural gas in a typical United States pipeline can be from zero to about 1 percent or more, though by commercial specification often can be up to 2 percent and sometime higher. The amount of CO2 that is soluble is given on specific demand. For example, if the PLNG is stored at 16 bar-g (17 bar absolute), its temperature should be in the range of −112° C. (161 Kelvin) and could have up to about 1.6 to 1.7% CO2 before solid CO2 would be expected to exist in the LNG tank. For PLNG stored at 10 bar-g (11 bar absolute) then the PLNG temperature may be in the range of −122° C. (151 K), and solid CO2 may exist if it was in the of 0.8 to 1% or more of the inlet gas. Whether or not CO2 is predicted to freeze in the PLNG storage condition, it need not be removed from the inlet gas in the methods and systems of the present disclosure. For example, cither a) its concentration is low enough that it will not form, or b) it may form and fall to the bottom of the storage tank and remain there until the tank is warmed, in which case it would depart with the export gas; or c) the timing of gas import can be managed so that gas is not imported for PLNG liquefaction at times when the CO2 concentration is such that it is predicted to freeze at PLNG conditions. If solid CO2 forms in the heat exchange equipment, there are a number of ways that it can be managed, for example, it can be CO2-defrosted at times when the liquefaction equipment is not in operation, that is, more PLNG volume is not being added to storage, or parallel heat exchange equipment can be installed and cycled for CO2 defrosting.


It is possible to adjust most existing processes for producing an LNG product at near atmospheric pressure and −162° C. (−262 F) to operate in the methods and systems of the present disclosure, i.e., to produce a pressurized LNG product at greater than 2 bar and perhaps more desirable at 4 to 20 bar or more. The methods and systems of the present disclosure may include one or more of these processes. These processes include: cascade refrigeration processes of one or more near pure components such as propane, ethane, ethylene, carbon dioxide, methane (the latter which could be in an open or closed loop configuration), etc.; any of the variations of single-mixed refrigeration processes including those known as PRICO, IPSMR, IPSMR+, etc., where the mixed refrigerant may be comprised of nitrogen, methane, ethane, ethylene, propane, propylene, compounds with four or more carbons, carbon dioxide, etc.; propane precooled mixed refrigeration process; dual-mixed refrigerant processes included those known as DMR, EMR, etc.; processes based on closed-loop expansion cycle(s) with nitrogen as the working fluid such as a reverse Brayton nitrogen cycle; processes based on closed-loop expansion cycle(s) with predominantly methane as the working fluid; expansion cycles with either nitrogen and or predominantly methane as the respective cycle working fluids; an open loop expansion cycle using components of the inlet gas as the working fluid; any precooled variant of an expansion cycle, etc.; any of the above which may boost the inlet gas as available to a higher pressure which often results in a net power reduction for the liquefaction after taking into account the power of the inlet compression; and any process with or without any of the above which takes advantage of pressure drop normally available from a high pressure natural gas source such as a natural gas transmission line down to a lower pressure, be it that of a local or regional distribution grid operating at lower pressure, PLNG storage conditions, etc.


The heat exchange for the liquefaction process of the present disclosure may use any heat exchange known for any LNG process, with the mechanical ratings and physical arrangement configured for the altered process conditions. Such heat exchangers could be specified as any number and variant of shell and tube, brazed aluminum heat exchanger (BAHX), spiral/coil wound heat exchanger (SWHW, CWHX), and the like.



FIGS. 3a-3k illustrates an exemplary cryogenic process in an embodiment of producing PLNG stored at a pressure of 16 bar-gage (17 bar absolute). Notably, FIGS. 3a-3c show a process flow diagram of a system for producing PLNG. Wherein, FIG. 3a shows a sectional flow diagram of the exemplary process before stream 9 (e.g., a flow after gas dehydration); FIG. 3b shows a sectional flow diagram of the exemplary process including stream 9, stream 10 (e.g., a flow after a single or mixed cooling/refrigerant procedure), and stream 11 (e.g., a flow after an expansion or de-pressurization); FIG. 3c shows a sectional flow diagram of the exemplary process after stream 11. More details are disclosed with the illustration of FIGS. 3d-3f.


Accordingly, FIGS. 3d-3f show exemplary process flow diagrams for a system for producing PLNG with corresponding annotations for different units. The exemplary process may include, but is not limited to, the following procedures: dehydration, liquefaction, pressurized storage, vaporization, and vapor management. The pipeline(s) supply a gas flow from power plant to 35° C.). All detailed features for the feeding stream are included in Table 1. The feeding stream 1 can be mixed with dehydrated-recycled flow in unit MIX-103, resulting in mixed stream 2. Stream 2 undergoes dehydration on dehydration beds. Stream 3, separated from the dehydrated flow, is streamed into a junction unit TEE-100 for further processes, such as blowing and/or drying, to generate stream 9 (Pressure at 5950 kPa, 35° C.). Notably, Stream 9 maintains the same temperature with steam 1 and stream 2, without being streamed into heat exchanger.



FIG. 3e illustrates a sectional view of the process flow diagram for the liquefaction stage. In this section, Stream 9 is directed to a liquefaction unit (e.g., LNG-100). After liquefaction, Stream 10 is routed to an expansion unit (e.g., kW-LNG-Exp), as depicted in the figure. Following expansion, Stream 11 is reduced in pressure to approximately 1700 kPa and cooled to −115.6° C. This stream may then enter a storage unit (e.g., ST-SLN-001) for pressurized storage, as shown in FIG. 3f.


Once stored, the LNG can either be vaporized via a heat exchanger for gas export or managed through a heat exchanger and reactor. Importantly, the stream generated from the vapor management process can be recovered at a temperature of 40° C. and a pressure of 6200 kPa, making it suitable for direct industrial use, as shown in FIG. 3f.



FIGS. 3g-3h show a process flow diagram for the dehydration unit and its processes, showing a flow for 10% of feed gas recycled to front end. As described above in FIGS. 3a-3c, Stream 1, as the feeding stream, is turned into stream 9 after the dehydration. FIG. 3h shows the engineering parameters for stream 9. An exemplary feed stream after dehydration in the disclosure can be characterized by a vapor/phase fraction of 1.0000, a temperature of 35.00°° C., and a pressure of 5950 kPa. It has a molar flow rate of 339.4 kgmole/h and a mass flow rate of 5632 kg/h. The molar enthalpy is −77,970 kJ/kgmole, while the molar entropy is 149.7 kJ/kgmole·C. The heat flow associated with this stream is −26,460,000 kJ/h. It operates under the fluid package Basis-1, with a standard ideal liquid volume flow of 18.34 m3/m and a liquid volume flow at standard conditions of 8005 m3/h. The stream can have the following components in mole fractions: H2O substantially at 0, nitrogen at 0.0050, CO2 at 0.0080, methane at 0.9700, ethane at 0.0153, propane at 0.0014, n-butane at 0.0002, i-butane at 0.0000, i-pentane at 0.0000, and n-pentane at 0.0000. These values illustrate the composition of the stream, with methane being the predominant component.



FIG. 3i shows a process flow diagram of a dehydration unit 300 with at least a molecular sieve 302. This unit 300 is designed to remove moisture from gas streams to ensure optimal conditions for downstream processes. The diagram illustrates the key components, including the feed inlet 304, which introduces the feed gas stream 310, probably containing water vapor, and the molecular sieve bed including the molecular sieve 302, where dehydration occurs. In certain embodiments, within the molecular sieve 302, the stream passes through a material with uniform pores that selectively adsorbs water molecules while allowing other gas components to flow through. The process typically includes a regeneration phase, where the adsorbed moisture is removed from the sieve 302, often involving heat or a purge gas. The dehydrated gas stream is then directed to downstream units 306a, 306b, and 306c, improving the efficiency and safety of subsequent processing stages.



FIG. 3j shows a process flow diagram view for the liquefication cooling unit and its process. Inlet stream 9 is after gas dehydration. Vapor Management (also known as Boil Off Gas, “BOG”) System is moving vapor being displaced in the tank by produced PLNG through heating and compression to export. In certain embodiments, it is being compressed before export. In this mode PLNG is just stored, and not pumped, vaporized, and sent to export.



FIG. 3k shows a process flow diagram for the pressurization and vaporization units and processes involved in LNG operations. These units include key components such as the LNG pump, which is responsible for transferring liquefied natural gas at high pressure, facilitating efficient flow through the system. The diagram also features a vaporizer, where the pressurized LNG is converted back into gas for export. In certain embodiments, the vaporization process utilizes heat exchange methods to raise the temperature of the LNG, ensuring that it transitions from a liquid to a gaseous state before being sent to the gas export pipeline. The integration of these units facilitates the critical processes involved in transforming LNG for distribution and maintains optimal conditions throughout the pressurization and vaporization stages.



FIGS. 4a-4e show a process flow diagram for producing a PLNG product at 16 bar-g with single mixed refrigerant process in alternative embodiment of the disclosure, wherein a molecular sieve is included in dehydration unit, and a vapor management system (in this case with compression) is integrated, and PLNG pumping and vaporization on stand-by as tank fills is included. Similar to the previous process shown in FIGS. 3a-3c, the process in the embodiment includes provisions for PLNG pumping and vaporization on standby while the storage tank is filling, ensuring that excess vapor can be managed without interruption. As the mixed refrigerant process operates, the seamless coordination between dehydration (shown in FIGS. 4a-4b), liquefaction (shown in FIG. 4c), vapor management (shown in FIG. 4d), vaporization (shown in FIG. 4e), and product storage is realized. Notably, two separate heat flows at different amount (e.g., kW-Refrig-1 at 2.1e+006 and kW-Refrig-2 1.783e+006) are feed, followed by heat exchange.


As detailed, FIGS. 4f-4j show a perspective view for liquefaction process, following the above single mixed refrigerant, where during tank filling: a) BOG compressor operates to move displaced vapor to export; and b) PLNG is not pumped, vaporized, and sent to export. This operational strategy allows for optimal management of both liquid and vapor phases, enhancing the overall efficiency of the liquefaction process while maintaining system integrity.


Alternatively, FIGS. 5a-5b show another process flow diagram for producing a PLNG product at 16 bar-g with another single mixed refrigerant process in alternative embodiment of the disclosure. Notably, though the embodiment employs less tanks for storage, reactions, and separation, the configuration secures liquefaction and vapor export for efficiency. This design is noteworthy for its streamlined approach, employing fewer tanks for storage, reactions, and separation compared to traditional configurations.


The condition of the feed stream after water dehydration (Stream 9) is given in Table 1.









TABLE 1





Feed Stream Conditions


















Flow Rate
339.4 kg mole/h



Temperature
35 C.



Pressure
 5950 kPa



Component
Mole Fraction



Water
   1 ppm max



Nitrogen
0.0002



Methane
0.9650



Ethane
0.0130



Propane
0.0080



i-Butane
0.0030



n-Butane
0.0040



C5+
Negligible









The single mixed refrigerant process cools the inlet stream to a temperature of −113° C., stream 10. There has been some modest pressure drop through the chilling equipment, for example, somewhere around 59 kPa. Thereby the chilled, pressurized fluid is let down in pressure through an expansion devise such as a throttle valve or, as shown in FIGS. 3a-3c, a hydraulic turbine (kW-LNG-Exp). Sufficient cooling was provided in the chilling process such that when the fluid is expanded to 1700 kPa (16 bar-gage), no vapor (typically referred to as “boil-off gas” or, simply, “BOG”) evolves off the storage tank. The fluid expanded to 1700 kPa through the hydraulic turbine is predicted to be at −115.5° C. and not evolve any BOG as sufficient chilling was accomplished to prevent BOG formation after expansion.


Typical large, site-built storage tanks for holding tens to hundreds of thousand cubic meters of LNG, such as used in the supply chain of international LNG, typically have a pressure rating of a bit over atmospheric pressure. In addition, the makers of cryogenic equipment also manufacture tanks with range of Maximum Available Working Pressures (MAWP) for storing LNG, e.g., 5 bar, 12 bar, and higher, with holding capacity of up to a few hundred and even a few thousand cubic meters. Storage tanks with a 5 and 12 bar MAWP can be operated as production vessels by those skilled in the art at some pressure below its MAWP, say 3 and 10 bar or higher, respectively.


For example, for PLNG storage in certain embodiments, the MAWP can be applicable for 20 bar-gage or more so that can be operated at, say, 16 bar-gage.


Illustrated in FIGS. 3a-3k, cryogenic storage tanks typically are designed for very low heat leak from the surroundings into the cryogenic fluid through approaches such as insulation, vacuum jacketing, etc. Still, there will be modest heat leak. Over time, if the tank is maintained at constant pressure, the heat leak may lead to evolving boil off gas, typically referred to as BOG.


BOG generated from heat leak is envisioned to be managed with near zero scope 1 emission via a number of means. One method in this disclosure is through a vapor management system 212. This system may heat and boost the pressure of the BOG in various sequence before returning natural gas at conditions equivalent to the operation of the local natural gas pipelines.


Another means to manage BOG is supplemental refrigeration to be added to the storage systems to mitigate the heat leak. This can be delivered via a heat exchange devise submerged into the PLGN products being stored. Or this can be provided by conduction to the system between the external wall of the storage tank and the insulation. Or such can be provided on BOG exiting the storage tank, the BOG being reliquefied, and returned to the tank. Another method to mitigate BOG formed via heat leak to the tank is to use the cold BOG to liquefy a small slip-stream of the inlet to capture the cold of the BOG before it is sent to export or, if compressed, a higher pressure higher than PLNG storage pressure.


Illustrated in FIG. 1, a vaporization unit 108 is located downstream of the pressurized storage unit 106 for releasing and supplying the fuel resource to a consumer on demand. Vaporizer types that have practically zero scope 1 emissions may be used, such as: ambient air vaporizers; once-throug flowing liquid vaporizers using river or sea water, e.g., open rack vaporizers; circulating liquid vaporizers using water or fluid mixtures such as glycol-water and heat provided into the system from waste and or ambient heat sources; all electric vaporizers; or water/fluid bath vaporizers, etc. Also note that some of the above do not use electricity directly for heat, such as ambient vaporizers, water/fluid bed vaporizers, and once through and or circulating liquid vaporizers have relatively low power draw for liquid movement but not for heat. Where electricity is used directly or indirectly for vaporization, low scope 2 electricity can be sourced. Selectively, the vaporization unit 108 may be connected with a signal unit, thereby determining a threshold of vaporization.


If natural gas export pressure is to be higher than the pressure of the liquified natural gas in storage, then a pump or a series of pumps can be used to get the fuel to the customer at full pressure after taking account of the pressure drop in the vaporizer and all other equipment, piping, and instrumentation that may be in line to the fuel consumers. The pumps may be located in the storage tank, that is, a type of submerged pump, or external to the storage tank, or both. If more than one pump is used, those pumps can be arranged in series and or in parallel. Furthermore, one of outputs of the system may be connected into a dispatchment system, which is used to dispatch the natural gas at a rate that matches demands in the industry or to an on-site or off-site consumer.


Additionally, an automation unit 110 may be integrated into the system 100 via a connection to all units and components of the envisioned systems and to data sources outside the system. The automation unit 110 may include a data processor, machine learning processor, and artificial intelligence processor, and the like.


In some embodiments, the automation unit 110 may optimize scope 1 and scope 2 GHGe intensity. The data from electricity generation and market data can be acquired and processed by the automation unit 110 for facilitating for example, sourcing low-carbon intensity electricity, sourcing lower cost electricity and or natural gas, timing liquefaction operations to windows of lower cost electricity and or natural gas or some optimized combination of same, etc.


The automation unit 110 may determine a threshold value and rate for dispatching natural gas to downstream users and or customers at different scenarios. For example, thresholds and rates may be set in response to low pressure or reduced flow rates in gas supply pipelines, indicating fuel supply constraints due to physical, contractual, or operational limitations. Another example includes high spot prices for natural gas, where elevated fuel costs justify performing fuel cost arbitrage by utilizing stored natural gas as pressurized liquefied natural gas (PLNG).


For the embodiments for establishing automation system integrating an automation unit 110, a monitoring unit 114 can be set up for monitoring temperature and pressure for safety.


In one or more embodiments, the automation unit and associated components may


track and optimize a variety of key metrics including, but not limited to end-use or customer natural gas demand-such as gross natural gas demand, gross natural gas supply, natural gas fuel pressure, and loss of inlet flow-along with weather information and modeling data. Additionally, the system may monitor site operational Scope 1 and Scope 2 emissions and their measurable components, market electricity and natural gas prices, natural gas purchase volumes and timing, timely gas compositions (including energy and CO2 content), electricity purchase volumes and timing, and facility-specific operational parameters such as total power consumption, flow rates, temperature, and pressures.


In some embodiments, the liquefaction unit 104 may utilize cooling solely from ambient sources, e.g., air, water, and supplemental power from electricity unit 112. Meanwhile, the resultant water from cooling natural gas procedure may be recirculated to the electricity unit 112.


In some embodiments, the system 100 may be configured to integrate equipment with no continuous vapor emissions to the atmosphere and a significant reduction of fugitive emissions. For example, the equipment may include low fugitive emissions pressure relief devices, such as rupture pins, rupture disks, and low-leakage pressure release valves.



FIG. 2 shows an exemplary process 200 of storing and redeploying natural gas in some embodiments. The process 200 is designed to be suitable for a variety of applications, in power plants, local gas distribution systems, industrial facilities, commercial real estate, residential communities, and stand-alone entities such as residential and miscellaneous other buildings and applications.


At 202, dehydration of a gaseous fuel is performed. A gaseous fuel may be selected from any fuel that is eligible for a compression and liquefaction at appropriate temperature and pressure, e.g., gas substantially including methane. The gaseous fuel is introduced to a dehydrator at a rate. Selectively, before the dehydration, a general waste removal may be conducted to remove impurities including, but not limited to water, gas, and sulfur compounds, and any combination thereof. In some embodiments, no waste or impurity removal steps are performed.


At 204, liquefaction of the gaseous fuel is carried out. The liquefaction may include compression, cooling, and liquefaction. The gaseous fuel is compressed to raise its pressure and temperature, facilitating the cooling and conversion to a liquid state. Following the compression, the compressed gas is then cooled to cryogenic temperatures, typically around −162 degrees Celsius (−260degrees Fahrenheit) for natural gas. This cooling process is achieved using a series of heat exchangers and refrigerants, and may transform the gas into a dense, clear, colorless liquid, e.g., LNG. In some embodiments, liquefaction may be performed by chilling using cooling solely from ambient sources such as air and water and supplemental power solely from electricity sourced from low GHGe sources, to produce a liquid product having a temperature of about −112°° C. (−170 F) and a pressure sufficient for the liquid product to be at or below its bubble point temperature, thereby reducing its volume.


At 206, the liquefied gas may be pressurized and stored as a fluid. In some embodiments, controls on temperature and pressure of the liquefied fuel may be operated to preclude the freezing of the liquefied gas and any impurities therein. These impurities include, but are not limited to, carbon dioxide, benzene, other aromatic hydrocarbons, and other heavy hydrocarbons. By avoiding freezing of these impurities, no removal steps or equipment may be needed to remove those impurities. Therefore, the present disclosure is more reliable and efficient in reducing emissions, compared to the current technologies. In some embodiments, the pressurization storage can be implemented as given in the example below.


At 208, a vaporization of the pressurized liquefied fuel is performed. The vaporization may be executed by a reception of gaseous fuel demand signal, which may be delivered from fuel consumers. In some embodiments, a threshold for such a signal delivery may be determined on demand of fuel peak time. Further, the vaporization may be actuated using heating from ambient sources, e.g., air and water, or supplemental power from electricity sourced from other plants and sites.


Electricity for this system can be sourced with lower scope 1 and scope 2 greenhouse gas intensity such as solar photovoltaic production, wind power, nuclear power, or fossil fuel combustion with carbon capture and sequestration. In some embodiments, the power supply may be adapted to power availability, e.g., low emissions sources such as solar and wind power may be used when available. In some cases, liquefaction and/or vaporization may be performed off very low carbon intensity electricity, for example, only liquefying when renewable energy is available, be it photovoltaic solar when the sun is shining or wind power when wind is turning the wind turbines that are either physically or virtually supplying the plant, coupled to the timing of gas offtake from the natural gas pipeline supply.


At 210, a redeployment of the vaporized gaseous fuel is performed to match demand. The redeployment can transport and distribute fuel to end-users, which can include power plants, industrial facilities, residential areas, etc. In some embodiments, to integrate a redeployment, a monitoring may be performed for safety. The monitoring may include a monitoring on temperature and pressure to prevent a leakage or accident.


As described in the storage and redeployment system 100, an automation system may be integrated into the system to achieve automatic management for the method and system. In the automation procedure, data can be collected and processed in computing module/processors therein, e.g., machine learning and artificial intelligence.


Another objective of the process 200 is to ensure that there are no continuous vapor emissions to the atmosphere other than fugitive emissions, and a minimization of fugitive emissions.


Therefore, a configuration of the process and system is specialized to enhance the above objective. For example, embodiments of the present disclosure may exclude certain features normally associated with natural gas and LNG operations. This can include omitting an amine system, which is commonly used for CO2 removal, concentration, venting, and the combustion of gas to destroy trace components in the CO2 stream co-absorbed by the amine solution. Additionally, embodiments may exclude fossil-fuel-fired eaters and engines. In certain embodiments, conventional relief valves, which may leak into the safety pressure relief device, can also be replaced with rupture disks or rupture pin devices. In further embodiments, instead of using hydrocarbon purge gas in the safety pressure relief device, system components may be designed to withstand pressures from potential deflagration events, or an inert gas such as nitrogen may be used to purge the system.


Minimization of the above systems results in a minimization of valves and other piping leak points of fugitive emissions. Features that may be included in embodiments of the present disclosure to further enhance these objectives include, but are not limited to, low leak and high integrity valves, using only ambient (air, water, geothermal) or electric heating, sourcing of low carbon intensity electricity.


In some embodiments, the gaseous fuel in the system and process may be a majority natural gas which is substantially methane along with other hydrocarbons, inert components, and contaminants. In addition, the method further includes a collection for export of gaseous fuel either not liquefied or counterpart liquefied yet through heat leaks converted back to gaseous state. Accordingly, the process can comprise an additional compression before gaseous fuel export for storage and redeployment afterwards.


In some embodiments, the methods and systems of the present disclosure may include capture and optimization of waste heat. Along with the utilization of power during the cooling and vaporization of the fuel, waste heat and water from other sources can be captured or circulated by the methods and systems of the present disclosure to increase energy availability and overall efficiency of the fluid, reduce hydrocarbon fuel consumption, or decrease power demand from external sources.


In some embodiments, the methods and systems of the present disclosure may include BOG Management, including embodiments whereby a refrigerant is used to offset heat leak. In some embodiments, the refrigerant may include liquid nitrogen. In some embodiments, the refrigerants may include one or more noble Gases such as Argon, Krypton, Neon, Xenon. In some embodiments, the liquid nitrogen is used to cool a heat exchanger embedded in the vapor space of the storage tank. In some embodiments, vapor circulated by a blower through heat exchanger using refrigerant(s) and condensed fluids are routed back to tank (can be by pressure or by pumping, etc.). In some embodiments, a drip back condenser may be used using elevation external to storage tank. In some embodiments, the heat exchanger is in the vapor space of the storage tank. In some embodiments, the methods and systems of the present may include a tank pressure-sensing mechanism and a device to throttle LIN appropriately to keep storage more than 90 or more than 120 days.


Therefore, the disclosed systems and methods are well adapted to attain the ends and advantages mentioned as well as those that are inherent therein. The particular embodiments disclosed above are illustrative only, as the teachings of the present disclosure may be modified and practiced in different but equivalent manners apparent to those skilled in the art having the benefit of the teachings herein. Furthermore, no limitations are intended to the details of construction or design herein shown, other than as described in the claims below. It is therefore evident that the particular illustrative embodiments disclosed above may be altered, combined, or modified and all such variations are considered within the scope of the present disclosure. The systems and methods illustratively disclosed herein may suitably be practiced in the absence of any element that is not specifically disclosed herein and any optional element disclosed herein. While compositions and methods are described in terms of “comprising,” “containing,” or “including” various components or steps, the compositions and methods can also “consist essentially of” or “consist of” the various components and steps. All numbers and ranges disclosed above may vary by some amount. Whenever a numerical range with a lower limit and an upper limit is disclosed, any number and any included range falling within the range is specifically disclosed. In particular, every range of values (of the form, “from about a to about b,” or, equivalently, “from approximately a to b,” or, equivalently, “from approximately a-b”) disclosed herein is to be understood to set forth every number and range encompassed within the broader range of values. Also, the terms in the claims have their plain, ordinary meaning unless otherwise explicitly and clearly defined by the patentee. Moreover, the indefinite articles “a” or “an,” as used in the claims, are defined herein to mean one or more than one of the elements that it introduces.


EXAMPLE

A combined cycle power generation plant whose 993 MW all-in capacity rating (just shy of a full gigawatt rating) is composed of two natural gas fired gas turbines coupled with waste heat recovery to generate steam to drive one steam turbine. With its modern equipment and arrangement, the plant can be operated in the region of 60% or more thermal efficiency. A typical heat rate may be 5,950 kJ/kWh net energy content (5,640 BTU/kWh “lower heating value” basis) with its electricity generated at 60 Hz. A typical US natural gas pipeline may be carrying a gas of composition mostly methane with some smaller amounts of nitrogen, CO2, ethane, propane, heavier hydrocarbons, and impurities. At typical net energy content of 910 BTU per standard cubic foot (gross energy content of 1010 BTU per standard cubic foot) the power plant may consume on the order of 148 million standard cubic feet a day (MMscfd) of natural gas.


Typically, the operator wishes to greatly reduce the probability of natural gas supply interruptions during the times when weather and other incidents may create a large grid-wide demand and or when grid power supplies are curtailed for one reason or another. The operator also wishes to reduce or totally eliminate all onsite combustion for natural gas storage and subsequent dispatch such as: amine reboilers, dehydration unit heat, compressor or generator drives, and practically always an overpressure relief system with a flare header using purge gas and a pilot flame system. Some LNG vaporization facilities combust part of the natural gas product stream.


On the contrary, the traditional process does not have the above outcomes. Typically, there are several problems therein. For example, venting of CO2 removed upstream of liquefaction occurs in all known liquefied natural gas production facilities if the CO2 content in the inlet is much above 50 to 100 ppm CO2. Also, standard practices have led to measurement of three to seven percent methane leakage for some natural gas handling facilities, through it has been proposed that one percent may be obtainable.


Table 2 is the basis of the analysis on fugitive methane emissions.












TABLE 2








Production Rate
100,000
gallons/day



Inlet Gas
339.43
Kgmole/h



C1
0.9700
mole %



CO2
0.0080
mole %







GHGe (20 years)











C1
72
ton CO2e(20)



CO2
1
ton CO2e(20)







GHGe (100 years)











C1
25
ton CO2e(20)



CO2
1
ton CO2e(20)









By applying the methods and systems of the present disclosure, the operator can derive the following GHGe benefits as listed in Table 3 versus traditional LNG storage at about atmospheric pressure, conventionally procured power from the grid. Also, an enhanced and certified methods for methane fugitive emissions control in the present disclosure versus historical practices is present in an example, showing cumulatively this disclosed method in reducing Scope 1 and scope 3 GHGe emission in excess of 90% for the gas storage facility. With design optimization it may be possible to potentially achieve in excess of 95% reduction.














TABLE 3








LNG at zero
LNG at 10
LNG at 16


Product


bar-g
bar-g
bar-g







Methane Fugitive Emissions Rate


3%
0.20%
0.20%


Dehydration by Mole Sieve
Fired

Yes
No
No



Heater






CO2 Removal by Amine
Fired

Yes
Not
Not



Reboiler


Applicable
Applicable


CO2 Vent with Incineration


Yes
No
No


Electricity Demand: Heaters,
MW

2.98
2.23
1.85


Rotating Equipment







Purchased Power Basis


ERCOT
Low Carbon
Low Carbon






PPA
PPA


Other Power Option


N.A.
Onsite
Onsite






Renewable
Renewable


Operating Power CO2 intensity
lb CO2/

800
~0
~0



MWh











GHGe Yearly Emissions-Scenario Comparison












GHGe (20 years)
Scope 1
tons/yr
112,773
7,352
7,352




CO2e





GHGe (20 years)
Scope 2
tons/yr
10,458






CO2e





GHGe (20 years)
Total
tons/yr
123,231
7,352
7,352




CO2e





GHGe (100 years)
Scope 1
tons/yr
40,330
2,554
2,554




CO2e





GHGe (100 years)
Scope 2
tons/yr
10,458






CO2e





GHGe (100 years)
Total
tons/yr
50,788
2,554
2,554




CO2e










Reduction versus Base












GHGe (20 years)
Scope 1
tons/yr
Base
6.5%
6.5%




CO2e





GHGe (20 years)
Scope 2
tons/yr
Base
0.0%
0.0%




CO2e





GHGe (20 years)
Total
tons/yr
Base
6.0%
6.0%




CO2e





GHGe (100 years)
Scope 1
tons/yr
Base
6.3%
6.3%




CO2e





GHGe (100 years)
Scope 2
tons/yr
Base
0.0%
0.0%




CO2e





GHGe (100 years)
Total
tons/yr
Base
5.0%
5.0%




CO2e









Further, the GHGe intensity is favorable when it is examined compared to the PLNG that is stored day in and day out during a year. per Table 4.











TABLE 4







PLNG Storage Volume
32,487
cubic meters


Stored PLNG, kg
11,284,647
kg


Fueled stored
24,877
tons


Fueled stored
9,080,107
ton-days/yr


GHGe (20 years)
7,352
ton CO2e(20)/yr


GHGe (100 years)
2,552
ton CO2e(20)/yr


Fuel storage GHG(20)
0.08%
ton CO2e/ton-days


intensity




Fuel storage GHG(100)
0.03%
ton CO2e/ton-days


intensity











While other operators in the art cite targets to get to a methane intensity of 0.2%, the operator in the disclosure could use the configurations of methods of this disclosure to have a technically assured way of meeting and exceeding those targets. With this disclosed method, the operator can select and derive the following, but not limiting to, parameters for their gas storage system: 1) 32,500 m3 (8.6 million gallons) of pressurized liquefied natural gas (PLNG) storage, which can provide 4 days of power plant fuel supply if the plant is operating at full rated power. Storage was selected to be at 16 bar-g (17 bar-a, 1700 kPa, about 250 psia). The tank was selected to have a higher pressure for its MAWP, in this case 18 bag-g. 2) Liquefaction can be in a unit capable of producing 100,000 actual US gallons per day of pressurized LNG. A unit much larger or smaller could have been specified. In this case this size would be selected since it results in reasonable number of days to refill the tank depending on how much fuel was withdrawn for use, on the order of less than 22 days if one full day of fuel was previously withdrawn, up to less than 90 days if a very severe event caused a full four days of withdrawals, as per Table 5.









TABLE 5







Power Plant Basis












Capacity
993
MW


Cycle

Combined Cycle


Configuration

2 Gas Turbines, 1 Steam




Turbine


Heat Rate
5639
BTU/kWh


PLNG-16 Liquefier Capacity:
100,000
gallons per day at 16 bar-g




(1700 kPa)










Fuel Storage Scenarios














Days of Storage to refill
1
2
3
4


Gallons, Million
2.1
4.3
6.4
8.6


m3
8,107
16,214
24,320
32,427


Days to fill with PNLG at
21.4
42.8
64.2
85.6


16 bar-g at a rate of 100,000






actual gallons per day.









Pumping and vaporization of the PLNG at 178 MMscfd, that is, the full fuel rate and system inlet pressure for the power plant fuel system, is equivalent to sourcing from the gas distribution pipeline(s).


In some embodiments, the design is powered by electricity for rotating equipment and heating to temperatures and or above ambient and for LNG/send out gas heating, including lower temperature heat sourced from ambient, e.g. air, water, geothermal, pressure available in the inlet natural gas stream, or various methods of internal heat transfer and power recapture from pressure let down devices.


A vapor management system may perform the at least following functions: 1) as the storage is filled with PLNG, it displaces vapor. The vapor management system warms the vapor, and either run it to export at a pressure below PLNG storage if a local customer is willing to accept, or it is compressed to the normal operating pressure(s) of the pipelines supplying the power plant so that the power generation facility may use it for fuel; while cryogenic liquid storage uses a number of methods to prevent heat leak, it still occurs though it has been minimized. A typical range of heat leak is on the order to cause boil off of 0.01% by weight of the tank contents up to 0.1% by weight or more. Filled tanks tend to have lower weight percent boil offs and near empty tanks tend to have higher rate of boil off.


A gas dehydration system may be used to treat the inlet gas down to a specification of less than one part per million water, in this case using molecular sieve whereby about 10% of the feed gas is used in the dehydration process and recycled to the fuel storage facility inlet. The system will use electricity to heat the natural gas circulating to regenerate the mole sieve beds rather than the traditional fired heater.


This example includes no intentionally designed-in scope 1 emissions and routine venting of natural gas.


In certain embodiments, fugitive emissions detection systems are included to reduce inadvertent methane emissions to the bar set by certifying parties, typically below 0.2% of throughput and possibly lower. A battery of various detection devices will be installed in the facility to excessive leakage above de minimis.


In certain embodiments, the system incorporates comprehensive safety pressure relief capabilities without using active header purging with natural gas or an active pilot flame. It employs rupture pin devices and burst plates to prevent gas leaks that could occur with standard pressure relief valves. Instead of natural gas, nitrogen is used for the safety pressure relief piping header. Additionally, an auto ignition device can be activated upon detecting pressure relief, utilizing direct or indirect measurement methods such as pressure waves or acoustic signals.


In certain embodiments, a procurement management system is in place to optimize several factors, including the carbon intensity of purchased power to reduce scope 2 greenhouse gas emissions, electricity costs, the cost of gas purchased for storage, and the revenue generated from selling power when accessing the stored fuel.


Representative operating conditions along the inlet and liquefaction processes are in listed Table 6, with reference to FIGS. 3a-3k:













TABLE 6







After
After
After




Dehydration
Liquefaction
Expansion




Before
Before
Before



Inlet
Liquefaction
Expansion
Storage



















Stream #
1
9
10
11


T, C
35.0
35.0
−113.0
−115.6


P, kPa
6,200
5,950
5,910
1,700


Kg · mole/h
339.43
339.43
339.43
339.43


kg/h
5,632
5,632
5,632
5,632


Std. Gas Flow,
6.802





MMscfd






Act. Liq. Flow,



15.768


m3/h






Act. Liq. Flow,



39.43


gpm











Dry basis Mole Fraction











N2
0.0050
0.0050
0.0050
0.0050


CO2
0.0080
0.0080
0.0080
0.0080


C1
0.9700
0.9700
0.9700
0.9700


C2
0.0153
0.0153
0.0153
0.0153


C3
0.0014
0.0014
0.0014
0.0014


iC4
0.0001
0.0001
0.0001
0.0001


nC4
0.0002
0.0002
0.0002
0.0002


iC5
trace
trace
trace
trace


nC5
trace
trace
trace
trace


C6+
trace
trace
trace
trace


Total, Dry basis
1.0000
1.0000
1.0000
1.0000


Water Content
7 lbs/
<1 ppm
<1 ppm
<1 ppm



MMscf









The pipeline(s) supplying the power plant typically operate at about 6200 kPa (62 bar-a) at the power plant fence line. It is at that point that natural gas will be brought into the fuel storage facility, as stream 1 (as shown in FIGS. 3a-3c).


Note that while the CO2 content in stream 1 is only 0.0080 mole fraction (0.8 mole percent), such is also 8,000 parts per million (ppm) CO2, far in excess of the established LNG process licensors specification to remove CO2 to the range of 50 to 100 ppm before liquefaction.


Pipelined natural gas typically has a low water content, for example, 7 pounds of water per million standard cubic feet of gas, to prevent gas transmission freeze-up in winter. Such is not low enough to prevent water freezing in the envisioned cryogenic operating temperatures. Therefore, a molecular sieve system with solid beds alternately dehydrating will be used to reduce the water content to less than one part per million at the outlet of the dehydration system as stream 9 (with reference to FIGS. 3d-3f).


Notably, the CO2 content in stream 9 is on the order of 0.0080 mole fraction (8,000 ppm).


From here, the dehydrated natural gas is taken to a liquefaction process 204 where it is chilled and subcooled to temperature of −113 C, stream 10. Other temperatures may be appropriate depending on the species in the gas to be liquefied. At this point there has been a minor pressure drop that has occurred through the piping and heat exchange equipment.


The liquefaction process is competed when the chilled fluid is expanded, in this case by a hydraulic turbine though it could be another devise such as a valve, to a tank operating at a discretionary pressure of 16 bar-g (1700 kPa). Another tank operating pressure can be selected, for example for PLNG as low as 2 bar-g or up to 20 bar-g or even higher up to the fluid critical pressure, e.g., 46.5 bar-a for pure methane.


Because the fluid was subcooled during heat exchange, no vapor is formed in or after


the expansion process, stream 11 (FIGS. 3d-3f). Avoiding flashing vapor after pressurized LNG expansion reduces the flow rates the vapor management system 212 must be designed to handle.


One or more tanks, either separate or interconnected, may be used for storing the PLNG, at conditions approximately equal to those in stream 11 in this particular example, illustrated in FIGS. 5a-5b.


With reference to FIG. 3k, the vaporization system in this example comprises a pump P-100 or a series of pumps, potentially arranged in parallel, either internal or external to the storage tank(s). During fuel send-out to customers, the rate of pumped PLNG from the tank can exceed 21 times the normal LNG production rate. This approach focuses on gradually building inventory while optimizing desired operating parameters, ensuring energy availability for the power plant even if supplies are curtailed or cut off for minutes, hours, or days, as detailed in Table 7.


Additionally, the system includes a vaporizer E-104, selected to utilize a series of ambient air vaporizers. These can operate continuously or in a cyclic manner to allow for defrosting. Alternative configurations may involve sourcing ambient heat by pumping a heating medium fluid and other means.












TABLE 7







After Pump
After



After Storage
Before
Vaporizer(s)



Before Pump
Vaporizer(s)
To Export







Stream #
ST-LNG-001
ST-LNG-002
ST-GasExport


T, C.
−115.6
−110.5
30


P, kPa
1,700
6,400
6,200


kgmole/h
7,371
7,371
7,371


kg/h
122,300
122,300
122,300


Std. Gas Flow,


147.7


MMscfd





Act. Liq. Flow, m3/h
342.5
339.2



Act. Liq. Flow, gpm
1508
1493








Mole Fraction, Dry Basis










N2
0.0050
0.0050
0.0050


CO2
0.0080
0.0080
0.0080


C1
0.9700
0.9700
0.9700


C2
0.0153
0.0153
0.0153


C3
0.0014
0.0014
0.0014


iC4
0.0001
0.0001
0.0001


nC4
0.0002
0.0002
0.0002


iC5
trace
trace
trace


nC5
trace
trace
trace


C6+
trace
trace
trace


Total, Dry basis
1.0000
1.0000
1.0000


Water Content
<1 ppm
<1 ppm
<1 ppm









The Vapor Management System 212 is configured to handle various scenarios, including the management of vapor space during LNG production and filling of the tank. In certain embodiments, when 15.77 m3 of PLNG is introduced into the tank, an equivalent volume of cold vapor must be managed as it displaces from the tank's top. These embodiments utilize a compressor to export the vapor at pressures aligned with the normal operating pressures of the sourcing pipeline. If a buyer can be secured for the gas at a pressure lower than the PLNG storage pressure, the need for compression in the vapor management system can be eliminated.


Additionally, effective tank pressure and vapor management are necessary for


balancing the vapor during the send-out of vaporized fuel, paralleling the management during PLNG production. Generally, CO2 concentration is not a significant concern since the gas used to fill the vapor space originates from the tank itself. The vaporized product in stream ST-GasExport (referenced in FIGS. 4a-4j and Table 8) can be utilized to fill the tank's vapor space as it is pumped out, and this gas can be chilled by cross-exchanging with the cold, pumped PLNG to dispatch.














TABLE 8










Vapor







Export



LNG into
Vapor from


During tank



Storage
storage


fill




















Stream #
11
ST-110
ST-111
ST-112
ST-113


T, C
−115.6
~−115
10
141
40


P, kPa
1,700
1,700
1650
6,300
6200


kgmole/h
339.43
26.8
26.8
26.8
26.8


kg/h
5,632
437.3
437.3
437.3
437.3


Std. Gas

0.5371
0.5371
0.5371
0.5371


Flow,







MMscfd







Act. Flow,
15.77
15.77
36.65
14.20
10.16


m3/h







Act. Flow,
39.43






gpm







Dry basis







Mole







Fraction







N2

0.0186
0.0186
0.0186
0.0186


CO2

0.0014
0.0014
0.0014
0.0014


C1

0.9791
0.9791
0.9791
0.9791


C2

0.0009
0.0009
0.0009
0.0009


C3

trace
trace
trace
trace


iC4

trace
trace
trace
trace


nC4

trace
trace
trace
trace


iC5

trace
trace
trace
trace


nC5

trace
trace
trace
trace


C6+

trace
trace
trace
trace


Total, Dry

1.0000
1.0000
1.0000
1.0000


basis







Water

<1 ppm
<1 ppm
<1 ppm
<1 ppm


Content



















TABLE 9








4 Days
32,427
m3 of



storage:

PLNG at





16 bar-g



PLNG
348
kg/m3



Density @





−111.5 C.





and 17 bar





Stored
11,284,647
kg



PLNG, kg





BOG
34.9
kW



Compressor





Minimum





Motor Size





Required
26.8
kg-mol/h



Capacity





Required
437
kg/hr



Capacity





Suction
1650
kPA



Pressure





Discharge
6300
kPA



Pressure


















TABLE 10







% BOG



Compressor



Utilization























BOG Low Rate
0.012%
weight
1,354
kg/d
56.42
kg/h
13%


(80% fill)

per day


BOG Rate at
0.026%

2,934
kg/d
122.25
kg/h
28%


50% filled


BOG Average
0.050%
weight
5,642
kg/d
235.10
kg/h
54%




per day


Without
0.093%
weight
10,483
kg/d
436.81
kg/h
100% 


upsizing BOG

per day


compressor


BOG High Rate
0.120%
weight
13,542
kg/d
564.23
kg/h
129% 


(10% fill)

per day








Claims
  • 1. A system for storing and redeploying a gaseous fuel, comprising: a dehydration unit configured to at least partially dehydrate the gaseous fuel,a liquefaction unit configured to liquefy the gaseous fuel,a pressurized storage unit configured to store the liquefied gaseous fuel, anda vaporization unit configured to vaporize the liquified gaseous fuel,wherein the pressurized storage unit is configured to control temperature and pressure therein to avoid operationally detrimental freezing of the liquefied gaseous fuel.
  • 2. The system of claim 1, wherein the temperature of the pressurized storage unit is maintained at or below the bubble point temperature of the gaseous fuel and between about 200 ka (29 psia) to about 4,480 kPa (650 psia).
  • 3. The system of claim 1, wherein the pressure of the pressurized storage unit is maintained from about 200 ka (29 psia) to about 4,480 kPa (650 psia).
  • 4. The system of claim 1, further comprising an automation unit for controlling one or more parts of the system.
  • 5. The system of claim 1, wherein the gaseous fuel substantially includes methane.
  • 6. The system of claim 1, wherein the system is configured for no direct, intentional or continuous vapor emissions to the atmosphere other than fugitive emissions.
  • 7. A method of storing and redeploying a gaseous fuel, comprising: dehydrating a gaseous fuel,liquefying the gaseous fuel,pressurizing the gaseous fuel for storage as a liquefied fuel,vaporizing the liquefied fuel to form a vaporized fuel, andredeploying the vaporized fuel,wherein the liquefied fuel is pressurized and stored at a combination of temperature and pressure that avoids operationally detrimental effects of freezing of any of the components in the liquefied fuel.
  • 8. The method of claim 7, wherein the vaporizing primarily uses heat from ambient heat sources, direct or indirect electricity, or a combination thereof.
  • 9. The method of claim 7, wherein the method is performed using power only from electricity, and not from combustion or emission-causing process.
  • 10. The method of claim 7, further comprising defrosting a cryogenic chilling equipment of any deposited solid CO2.
  • 11. The method of claim 10, wherein the defrosting is performed by a cycle operation.
  • 12. The method of claim 10, wherein the defrosting is performed by cycling more than one parallel chilling equipment.
  • 13. The method of claim 7, wherein contaminates are accumulated in a storage volume and returned to vapor or liquid when the storage volume is subsequently warmed.
  • 14. The method of claim 7 wherein the electricity used for the dehydration, liquefaction, storage and vaporization processes is at a lower carbon intensity than the electrically generally available from regional electricity supplies.
  • 15. The method of claim 14, wherein a timing of purchasing electricity is optimized to yield a lower carbon intensity then generally available from regional electricity supplies, even if the supply is coming from said regional electricity supplies.
  • 16. The method of claim 7, wherein fugitive emission is detected by a plurality of methane-in-air detection devices.
  • 17. The method of claim 16, wherein the methane-in-air detection devices are communicatively coupled to an automation unit.
  • 18. The method of claim 17, wherein the methane-in-air detection devices are deployed from land vehicles, drone, aircraft, and satellites, and communicatively coupled to an automation unit.
  • 19. The method of claim 14, wherein the purchasing of electricity and natural gas uses real time price information to optimize the cost intensity of the storage using automated and or semi-automated methods.
  • 20. The method of claim 19, wherein automated souring of electricity and natural gas is based, at least in part, on machine learning and artificial intelligence.
  • 21. The method of claim 7, wherein the gaseous fuel is only taken for storage when its composition is below the freezing saturation.
  • 22. The method of claim 1, wherein CO2 concentration is reduced by means of a membrane, chemical solution, or solid absorbent and the residue stream being compressed and sent to gas consumers.
  • 23. The method of claim 1, wherein CO2 concentration is reduced by means of a membrane, chemical solution, or solid absorbent and the residue stream is sent to sequestration.
  • 24. The method of claim 7, wherein the vaporizing primarily uses heat from waste heat sources.
  • 25. The method of claim 7, wherein the vaporizing primarily uses heat from low carbon intensity electricity.
  • 26. The system of claim 1, further comprising at least a safety pressure relief device that practically minimizes hydrocarbon leakage into the pressure safety header.
  • 27. The system of claim 26, wherein at least a rupture disk is incorporated for safety pressure relief.
  • 28. The system of claim 27, wherein the rupture disk and pressure safety device are incorporated in series for safety pressure relief.
  • 29. The system of claim 1, further comprising at least a safety pressure relief device operated without purge gas comprising natural gas.
  • 30. The system of claim 29, further comprising at least a mechanical element of the safety pressure relief device to withstand the overpressures from deflagration events.
  • 31. The system of claim 1, where there is no combustion equipment aside from pilot(s) at the end of safety pressure relief device.
  • 32. The system of claim 1, further comprising a vapor management device.
  • 33. The system of claim 32, wherein the vapor management system has at least a header operating at different pressures.
  • 34. The system of claim 32, wherein the vapor management system is configured to route vapor from maintenance depressing.
  • 35. The system of claim 32, wherein vapor in the vapor management system is routed to downstream gas consumers without the need for compression.
  • 36. The system of claim 32, wherein vapor in the vapor management system is compressed and routed to downstream gas consumers.
  • 37. The system of claim 32, where vapor in the vapor management system is condensed with a supplemental refrigeration and returned to the pressurized storage.
CROSS-REFERENCE

This U.S. Non-Provisional Application, claims priority to U.S. Provisional Application No. 63/595,557, filed on Nov. 2, 2023, the contents of which is incorporated herein by reference in its entirety.

Provisional Applications (1)
Number Date Country
63595557 Nov 2023 US