The technical field of this disclosure relates generally to storage tanks for storing fuel gas and, more particularly, to a system and method for filling a fuel gas storage tank.
The use of alternative fuel gasses as a fuel source for motor vehicle applications is gaining commercial traction. Natural gas, for example, is comprised primarily of methane (CH4) and, currently, can be combustibly consumed to power dedicated natural gas vehicles, which are fueled only by natural gas, or dual-fuel vehicles that are fueled by a combination of traditional petrol-based fuels and natural gas through separate fueling systems. Natural gas may be stored in an on-board fuel storage tank in two plausible ways: as compressed natural gas (CNG) or adsorbed natural gas (ANG). Compressed natural gas is natural gas that is contained within a tank—usually a cylindrical or spherical tank—at less than 1% of the volume it would normally occupy at standard temperature and pressure (STP). Tank pressures of 150 bar to 250 bar are typically needed to achieve this level of compression.
Adsorbed natural gas is natural gas that is stored in a solid state by way of adsorbtion onto a natural gas storage material housed within a tank. The natural gas storage material increases the volumetric and gravimetric energy density of the gas within the available tank space such that it compares favorably to CNG but at a much lower pressure of 60 bar or less. Several different kinds of natural gas storage materials are known in the art including activated carbon and, more recently, metal-organic-frameworks (MOFs) and porous polymer networks (PPNs) that have an affinity for natural gas. MOFs, in general, are high surface area coordination polymers having an inorganic-organic framework, often a three-dimensional network, that includes metal ions (or clusters) bound by organic ligands. Many different types of MOFs that are able to reversibly adsorb natural gas are commercially available in the marketplace and newly-identified MOFs are constantly being researched and developed.
Another type of alternative fuel gas is hydrogen, which, like natural gas, can also be stored in a compressed state or on a hydrogen storage material. Storing hydrogen gas in a solid state on a hydrogen storage material has similar thermodynamics to storing natural gas on an ANG storage material even though hydrogen uptake may be chemical in nature as opposed to adsorptive. Hydrogen gas, for instance, can be reversibly stored as a hydride on a hydrogen storage material such as a metal hydride or a complex metal hydride. One specific example of a suitable metal hydride is lithium hydride (LH). Complex metal hydrides may include various known alanates and amides. Some specific complex metal hydrides include sodium alanate (NaAlH4), lithium alanate (LiAlH4), magnesium nickel hydride (Mg2NiH4), and lithium amide (LiNH2). There are, of course, many other hydrogen storage materials that are commercially available.
While fuel gasses such as natural gas and hydrogen gas can be stored in a solid state at a lower pressure, compared to CNG, the time needed to fill a fuel gas storage tank that houses an appropriate fuel gas storage material can be extensive. Indeed, because the process of charging the fuel gas into the fuel gas storage material is exothermic—which in turn may limit the rate at which additional fuel gas is accrued and stored in a solid state—the time needed to charge enough fuel gas into a storage tank to provide a reasonable driving distance for a vehicle can last hours. Such long filling times may not necessarily be a problem for in-home or other overnight filling stations. They may, however, be unacceptable for filling stations that require faster filling times, such as commercial drive-up filling stations that service the public. Nonetheless, and no matter the circumstances, the ability to improve the rate at which solid state fuel gas storage can be achieved so as to reduce the time needed to fill an associated storage tank would make the use of fuel gas technologies a more attractive option for motor vehicle applications.
A system and method of for filling a fuel gas storage tank with a fuel gas, such as natural gas or hydrogen gas, is disclosed. The system includes a fuel gas storage tank that includes an inlet, an outlet, a fuel gas storage material within an interior of the storage tank, and at least one filter tube disposed within the tank interior and extending through the bulk of the fuel gas storage material. The filter tube fluidly communicates with at least one of the inlet and the outlet and defines a flow passage through which a flow of fuel gas can navigate. The filter tube, moreover, is permeable to fuel gas, meaning that fuel gas can diffuse from the flow passage inside the filter tube into the tank interior outside of the filter tube. Heat that is generated from the exothermic charging of the fuel gas into the fuel gas storage material can also be transferred from the interior of the tank into the flow passage where it can be absorbed by the fuel gas flow being guided through the filter tube. Multiple filter tubes may be disposed within the tank interior that communicate with one another. Additionally, the system includes an external flow path that can recirculate fuel gas from the tank inlet to the tank outlet, as well as a fuel gas charging amplifier located along the external flow path.
When filling the fuel gas storage tank with fuel gas, a flow of fuel gas is introduced into the inlet of the tank. The fuel gas flow then travels along the flow passage of the one or more filter tubes. As the flow of fuel gas travels along the flow passage, some of the fuel gas diffuses out of the filter tube and into the interior of the tank where it comes into contact with, and is charged into, the fuel gas storage material. At the same time, heat from the exothermic charging (adsorption, chemical uptake, or both) of the fuel gas into the fuel gas storage material is transferred from the interior of the tank to inside the filter tube in the opposite direction from the diffusing fuel gas. In this way, heat that is generated from charging of the fuel gas storage material can be absorbed by the flow of fuel gas traveling through the filter tube and eventually removed from the fuel gas storage tank through the tank outlet. The ability to remove generated heat from the fuel gas storage tank during filling can improve the rate at which fuel gas is charged into the fuel gas storage material and ultimately speed up the time it takes to fill the tank to the desired level.
The fuel gas charging amplifier located along the external flow path can be operated to reject the heat acquired by the flow of fuel before it is recirculated back into the fuel gas storage tank. The fuel gas charging amplifier may include a heat exchanger, a compressor, or both, among other possibilities. As such, the fuel gas charging amplifier can be controlled to change the pressure and/or reduce the temperature of the fuel gas flowing along the external flow path—and thus the one or more filter tubes—to exert influence over the rate at which fuel gas is being charged into the fuel gas storage material. And to help the fuel gas charging amplifier operate in a way that achieves the desired metrics for filling the fuel gas storage tank, a controller may interface with and control the fuel gas charging amplifier based on one or more measured characteristics of the fuel gas flow being directed along the external flow path as well as one or more measured characteristics of the fuel gas storage tank.
The system and methods of filling a fuel gas storage tank described below can be used with any tank structure that stores fuel gas at a relatively low pressure in a solid state. The fuel gas storage tank includes fuel gas storage material that permits a fuel gas, such as natural gas or hydrogen gas, to be stored at an energy density comparable to that of compressed fuel gas, but at lower tank pressure. For example, the amount of adsorbed natural gas (ANG) that can be stored on an ANG storage material at 35 bars of tank pressure is approximately the same as the amount of compressed natural gas that can be stored in a tank of the same volume at 240 bars of tank pressure. The following system and methods are useful to lessen or minimize the time required to fill the fuel gas storage tank by monitoring certain tank filling conditions and employing a fuel gas charging amplifier to boost the rate of adsorption and or chemical uptake of the fuel gas by the fuel gas storage material in the tank.
The fuel gas storage tank 12 includes a shell 22 at least partly defining an interior 24 of the tank 12 and fuel gas storage material 26 located within the interior 24 of the tank 12. The storage tank 12 also includes an inlet 28 and an outlet 30. At least one of the inlet 28 or the outlet 30, and preferably both, fluidly communicates with a filter tube 32. The filter tube 32, as shown, is disposed within the interior 24 of the storage tank 12 and defines a flow passage 40 on its inside. Fuel gas can flow within and along this flow passage 40 without having to directly contact and navigate through the bulk of the fuel gas storage material 26. As fuel gas flows along the flow passage 40—which may constitute at least part of the path between the tank inlet 28 and the tank outlet 30—a portion of the fuel gas diffuses through the filter tube 32 and into the region of the tank interior 24 occupied by the fuel gas storage material 26. The fuel gas that does not diffuse through the filter tube 32 eventually exits the tank 12 through the tank outlet 30 and continues on through the exterior flow path 14. The exterior flow path 14 fluidly connects the tank outlet 30 to the tank inlet 28 as part of a flow path that recirculates gas from the tank outlet 30 to the tank inlet 28.
In the schematic representation of
The fuel gas storage tank 12 is preferably constructed to have one inlet 28 and one outlet 30, but that is not necessarily required. The inlet 28 and the outlet 30 may be located at different ports on the tank shell 22 or, in other embodiments, they may be co-located at a common port so that only a single mating connector is needed to establish an operable connection with the external flow path 14. For instance, in the common port embodiment, the inlet 28 and outlet 30 may be arranged so that fuel gas flows in one direction through a first central opening in the port and in the opposite direction through a second peripheral opening in the port that is isolated from the first opening. Skilled artisans will know and understand the various ways to design and configure the tank inlet 28 and tank outlet 30 as part of the tank shell 22 and, as such, a more detailed description of their various configurations is not necessary here.
The fuel gas storage material 26 is located within the interior 24 of the tank 12 and outside of the filter tube 32. The fuel gas storage material 26 can be any material that is capable of reversibly storing the fuel gas in a solid state. Natural gas and hydrogen gas are two notable types of fuel gas that may be stored in such a way. Natural gas is a combustible fuel whose largest gaseous constituent is methane (CH4). The preferred type of natural gas that is employed in the filling system 10 is refined natural gas that includes 90 wt. % or greater, and preferably 95 wt. % or greater, methane. The other 5 wt. % or less may include varying amounts of natural impurities—such as other higher-molecular weight alkanes, carbon dioxide, and nitrogen—and/or added impurities. Hydrogen gas is also a well known combustible fuel having the chemical formula H2. The fuel gas storage material 26 may, accordingly, be an ANG storage material if the fuel gas is natural gas or a hydrogen storage material if the fuel gas is hydrogen gas.
An ANG storage material (for storing adsorbed natural gas) is typically a porous adsorbent material. It may be incorporated into the fuel gas storage tank 12 in granulized form, powderized form, or any other suitable form. The average particle size of the ANG storage material pieces may even change over time as those pieces undergo fragmentation as a result of thermal, pressure, and loading cycles. Some specific examples of materials that can comprise some or all of the ANG storage material are activated carbon, metal-organic-frameworks, or porous polymer networks. Activated carbon is a carbonaceous substance, typically charcoal, that has been “activated” by known physical or chemical techniques to increase its porosity and surface area. A metal-organic-framework, as mentioned before, is a high surface area coordination polymer having an inorganic-organic framework, often a three-dimensional network, that includes metal ions (or clusters) bound by organic ligands. A porous polymer network is a covalently-bonded organic or organic-inorganic interpenetrating polymer network that, like MOFs, provides a porous and typically three-dimensional molecular structure.
Any of a wide variety of MOFs and PPNs may be used as the ANG storage material. Some notable MOF's and PPN's that may be used as the ANG storage material are disclosed in R. J. Kuppler et al., Potential applications of metal organic frameworks, Coordination Chemistry Reviews 253 (2009) pp. 3042-66, D. Yuan et al., Highly Stable Porous Polymer Networks with Exceptionally High Gas-Uptake Capacities, Adv. Mater. 2011, vol. 23 pp. 3723-25, W. Lu et al., Porous Polymer Networks: Synthesis, Porosity, and Applications in Gas Storage/Separation, Chem. Mater. 2010, 22, 5964-72, and H. Wu et al., Metal-Organic Frameworks with Exceptionally High Methane Uptake: Where and How Methane is Stored?, Chem. Eur. J. 2010, 16, 5205-14. Of course, a wide variety of MOFs and PPNs are commercially available and suitable for use as the gas storage material 14, and many others are constantly being researched, developed, and brought to market.
A hydrogen storage material (for storing hydrogen gas) is also typically a porous material. Materials that can function as a hydrogen storage material generally have the ability to reversibly store hydrogen gas as a hydride through chemical uptake. These types of materials include metal hydrides and complex metal hydrides. One specific example of a suitable metal hydride includes lithium hydride (LH). Complex metal hydrides may include various known alanates and amides. Some specific complex metal hydrides include sodium alanate (NaAlH4), lithium alanate (LiAlH4), magnesium nickel hydride (Mg2NiH4), and lithium amide (LiNH2). There are, of course, many other hydrogen storage materials that are commercially available besides metal hydrides and complex metal hydrides. For example, MOFs and PPNs as referenced in the above literature may be used for hydrogen storage, although the storage mechanism associated with such materials is by way of adsorption rather than chemical uptake.
In one particular embodiment, as shown in
The structural wall 34 includes at least one opening 56 that communicates with the flow passage 40 so that fuel gas can pass through it. The at least one opening 56 can be an elongated slot or slots, a series of spaced apart round holes, or some other type of fuel gas navigable opening. As such, the structural wall 34 may be a tubular metal extrusion or casting having at least one elongated slot and/or a series of holes, or any other type of porous wall configuration, and it may be formed from stainless steel, an aluminum alloy, a plastic, or some other material of sufficient strength, durability, and thermal conductivity. While the exact size and construction of the structural wall 34 may vary based on the size and pressure constraints of the fuel gas storage tank 12, the type and quantity of the fuel gas storage material 26 contained within the tank 12, and a variety of other factors, the structural wall 34 is typically designed to have a diameter that ranges from about 5 mm to about 20 mm and a wall thickness that ranges from about 1 mm to about 10 mm. The openings 56, moreover, are typically sized to exclude the passage of granules, particles, or other pieces of the fuel storage material 26 that are sized above a certain particles size that may lie anywhere between about 10 μm to about 2 mm.
The membrane 36 is preferably a micro- or ultra-filtration material or film that is fuel gas permeable. The membrane 36 has a thickness that typically ranges from about 20 μm to about 2 mm, and includes a network of interconnected pores through its thickness to render the membrane 36 porous. The pores are sized to allow diffusion of the fuel gas from inside the flow passage 40 of the filter tube 32 to the fuel gas storage material 26 outside the filter tube 32. The pores may also be sized to prevent the passage of granules, particles, or other pieces of the fuel storage material 26 above a certain size—and which may be small enough to pass through the structural wall 34—from passing through the thickness of the membrane 36 and possibly entering the flow passage 40. An average pore size of about 10 μm to about 50 μm is typically sufficient in such circumstances, although greater and smaller pore sizes may be employed. While a number of micro- or ultra-filtration membranes exist and are known in the art to be fuel gas permeable, the membrane 36 included in the filter tube 32 is preferably a hydrophilic zeolite such as ZSM-5, which can help reduce water contamination of the fuel storage material 26, or an organic polymer-based membrane. The membrane 36 can be appended to the structural wall 34 by any known technique.
The structural wall 34 and the membrane 36 cooperate to perform a number of functions in this particular embodiment of the filter tube 32. First, the structural wall 34 and the membrane 36 allow fuel gas to diffuse out of the filter tube 32 and, as will be discussed below, allow heat to transfer into the filter tube 32. This cross-flow of fuel gas diffusion and heat transfer through the filter tube 32 helps improve the rate at which the fuel gas storage material can be charged with fuel gas. Second, the arrangement of the structural wall 34 and the membrane 36 relies on the structural wall 34 to bear most or all of the load from the surrounding fuel gas storage material 26 while additionally providing a barrier—i.e., the membrane 36—to prevent fractured or crumbled bits of the fuel storage material 26 above a certain size from passing through the filter tube 32 and into the flow passage 40. Keeping unacceptably-sized fuel gas storage material 26 from entering the flow passage 40 and being carried away by the flow of fuel gas G traveling along the flow passage 40 helps avoid loss of overall fuel gas storage capacity for the tank 12 as well as contamination or harm to other system components. Third, the membrane 36 can help control the quantity and kind of impurities that are introduced to the fuel gas storage material 26. Water, for example, which can occupy gas storage sites within the fuel gas storage material 26, can be selectively trapped by the membrane 36 if the membrane 36 contains or is formed from hydrophilic material like a zeolite.
The filter tube 32 can have other constructions besides the one just described yet still function in a similar manner. For example, as shown in
Still further, in another embodiment, the filter tube 32 may include the structural wall 34 without the additional membrane 36 or the mesh structure 58. In this embodiment, the openings defined by the structural wall 34 may themselves be sized to exclude all pieces of the fuel gas storage material 26 above a certain size from passing through it and entering the flow passage 40 of the filter tube 32. The structural wall 34, for example, can be provided with openings that are small enough to exclude the passage of fuel storage material pieces (granules, powder, etc.) from outside the filter tube 32 to inside the filter tube 32 while taking into account the fact that the average particle size and particle size distribution of the fuel storage material 26 may change over time as temperature, pressure, and load cycling during repeated filling and discharge cycles can lead to fragmentation of the fuel gas storage material 26. The structural wall 34 of this embodiment can have any of the above-mentioned constructions—e.g., a tubular metal extrusion or casting having at least one elongated slot and/or perforations, or any other type of porous wall configuration—and the size of its openings can vary depending on the composition and physical characteristics of the fuel gas storage material 26. In a preferred implementation, however, the openings defined in the structural wall 34 are sized to exclude pieces of the fuel gas storage material 26 above 10 μm, or in some instances above 50 μm, from passing through it and possibly entering the flow passage 40. The membrane 36 or the mesh structure 58 may also be used as the filter tube 32 in the absence of the structural wall 34, although they may have to be thicker than before if used in that scenario.
During a filling event, fuel gas is delivered to the filling system 10 by a fuel gas source 60. The fuel gas supplied by the fuel gas source 60 plus any fuel gas returning from the external flow path 14 provides the flow of fuel gas G that is fed to the storage tank 12. The fuel gas source 60 is preferably a tapped residential or commercial gas distribution network or a large underground storage tank that supplies fuel gas at a pressure ranging from about 1 bar to about 50 bar. It is also possible, as another example, for the fuel gas source 60 to be a compressed fuel gas tank that stores fuel gas at a pressure greater than 200 bar. The compressed fuel gas tank may be outfitted with a Joule-Thompson valve and an expansion tank that, together, throttle the compressed fuel gas to a lower pressure of about 1 bar to about 50 bar for delivery to the filling system 10. Still further, the fuel gas source 60 could be a cryogenic tank that holds liquefied fuel gas at a pressure of up to about 2 bar. A heat exchanger may be used in conjunction with the cryogenic tank to evaporate the liquified fuel gas for delivery to the filling system 10.
The flow of fuel gas G enters the storage tank 12 through the tank inlet 28 at an instantaneous mass flow rate Q′in, flows along the flow passage 40 of the filter tube 32, and exits the tank 12 through the tank outlet 30 at an instantaneous mass flow rate Q′out. As the fuel gas G flows along the flow passage 40 of the filter tube 32, some of the gas G′ diffuses through the filter tube 32 for charging (e.g., adsorption, chemical uptake) into the fuel storage material 26. The direction of fuel gas diffusion through the filter tube 32 is generally transverse to the direction of gas flow inside the filter tube 32 along the flow passage 40. In this arrangement, where the fuel gas G flowing into the storage tank 12 does not impinge or flow directly across the fuel storage material 26 and is only dispensed through the filter tube 32, the pressure required to direct the fuel gas flow G through the tank 12 is relatively low, and the diffused fuel gas G′ is charged more uniformly along the length of the filter tube 32 than if the gas flow G had been simply pumped into direct contact with the fuel gas storage material 26.
The process of charging fuel gas into the fuel gas storage material 26 is exothermic, meaning that thermal energy or heat is released from the fuel gas storage material 26 when fuel gas molecules (as well as other molecules) are acquired by the storage material 26 for solid state storage. As shown in
Thus, during tank filling, diffused fuel gas G′ and heat H are exchanged through the filter tube 32 and between the flow of fuel gas G in the flow passage 40 and the fuel gas storage material 26 located outside of the filter tube 32. It is not uncommon for the rate of fuel gas diffusion and heat transfer to vary along the length of the filter tube 32 as is shown schematically in
In the example of
Q
net
=Q
in
−Q
out
where Qnet is the amount of fuel gas charged during filling over a given time period, expressed in units of mass or moles. The cumulative values of Qin and Qout can be obtained by integrating the instantaneous fuel gas mass flow rates Q′in and Q′out or by referencing empirical data or other indicative information. The controller 18 can perform this function as will be described in more detail below.
The exothermic nature of the fuel gas charging process can limit the rate of fuel gas adsorption and the amount of fuel gas contained within the storage tank 12. This is true because the heat generated by the charging process (e.g., adsorption or chemical uptake) can raise the temperature of the fuel gas storage material 26 which, in turn, works to release some of the fuel gas. In other words, as the fuel gas storage material 26 increases in temperature during charging, the rate at which fuel gas is accumulated is reduced (i.e., the difference between the competing rates of fuel gas charging and release converge as the temperature of the fuel gas storage material 26 increases) unless the heat produced by the charging process can be rejected. Directing the flow of the fuel gas G through the storage tank 12 within the filter tube(s) 32, as illustrated in
Referring again to
In the filling system 10 illustrated in
The compressor 42 and the heat exchanger 44 can be operated by the controller 18 to control the flowrate (Qin and Q′out) and temperature of the flow of fuel gas G being passed through the storage tank 12 by way of the filter tube(s) 32. The heat exchanger 44 can decrease the temperature of the fuel gas flow G to within an operating range of, for example, about −50° C. to about 0° C. by extracting heat from the gas flow G with a coolant that simultaneously traverses the heat exchanger 44 in heat exchange relation with the fuel gas flow G. Decreasing the temperature of the flow of fuel gas G passing along the flow passage 40 of the filter tube 32 has the effect of increasing the temperature gradient between the fuel gas storage material 26 and the gas flow G, which thermodynamically favors the transfer of H through the filter tube 32 and into the fuel gas flow G as the heat is generated by fuel gas charging into the fuel gas storage material 26. As for the compressor 42, it can increase the pressure of the fuel gas flow G within an operating range of, for example, about 35 bars to about 50 bars if the fuel gas source 60 does not otherwise contribute that type of pressure. An increase in pressure of the fuel gas flow G speeds up its flowrate through the storage tank 12, the flow passage 40 of the filter tube 32, and the system 10. A greater flowrate of the fuel gas flow G, in turn, helps maintain the maximum desired temperature gradient between the fuel gas storage material 26 and the gas flow G by removing the transferred heat H from the interior 24 of the storage tank 12 more quickly. Though under the control of the controller 18 in the illustrated example, the compressor 42 and/or the heat exchanger 44 can operate in the absence of the controller 18, if desired; that is, they can simply be powered “on” during the filling event at a particular operational state (e.g., maximum pressure and maximum heat removal) and powered “off” afterwards without independent instruction from the controller 18.
The system 10 includes additional components, some of which provide information to the controller 18 with respect to the fuel gas flow G being passed through the system 10. The system 10 includes a first measurement device 46 located upstream from the fuel gas charging amplifier 16, a second measurement device 48 located downstream from the fuel gas charging amplifier 16, and a third measurement device 54 located at the storage tank 12. Each of the first and second measurement devices 46, 48 measures one or more characteristics of the fuel gas flow G being directed along the external flow path 14. The third measurement device 54 measures one or more characteristics of the storage tank 12. The controller 18 receives measurements from the measurement devices 46, 48, 54 and controls operation of the fuel gas charging amplifier 16 based at least in part on the received measurements. In the schematic representation of
Each of the first and second measurement devices 46, 48 preferably includes a flow meter or is a flow meter that measures the volumetric flow rate and/or the mass flow rate of the fuel gas flow G being directed along the external flow path 14 at the location of the respective device. The first and second flow devices 46, 48 may even be a single differential flow meter that measures the fuel gas flow G entering and exiting the storage tank 12 at a single location. Flow meters are useful for determining the amount of fuel gas being charged into the fuel gas storage material 26 by periodically or continuously measuring Qin and Q′out and providing those measurements to the controller 18. The controller 18 receives these measurements and determines the amount of fuel gas charged into the fuel gas storage material 26 during filling over a given period of time as described above (Qnet=Qin−Qout).
Each of the first and second measurement devices 46, 48 may be adapted, as individual or integrated components, to measure gas temperature, gas pressure, volumetric flow rate, mass flow rate, moisture content, or any combination of these or other gas characteristics at different locations of the fuel gas flow G within the filling system 10. For instance, in the illustrated example, the system 10 includes a drier 50 located along the external flow path 14 that is controlled by the controller 18. The controller 18 may receive moisture content measurements from one or both of the first and second measurement devices 46, 48 and, based on that data, can selectively operate the drier 50 to remove moisture from the fuel gas flow G. The controller 18 can receive information from any number of system devices, process the information, and control other system devices based on the processed information. The filling system 10 can include other components as well, such as the illustrated pre-filter 52 for additional impurity containment, valves, connectors, and additional controllers, to name but a few. The fuel gas charging amplifier 16 may also include additional components operable to increase the rate of natural gas adsorption by the ANG storage material 26.
The third measurement device 54 may be one or more sensors that measure the temperature and/or pressure of the interior 24 of the tank 12. Temperature and pressure measurements can be used to calculate or otherwise determine the amount of fuel gas consumed during vehicle operation and, consequently, the remaining amount of fuel gas stored in the fuel gas storage material 26 at a given time. In particular, the third measurement device 54 can gauge how much fuel gas is still present, Qstart, in the tank 12 just before filling is commenced. It can also be used to corroborate the fuel gas charging valuations (e.g., Qin, Qout, Qnet) obtained from measurements taken by the first and second measurement devices 46, 48 during the filling event. A separate controller (not shown) on-board the vehicle may monitor the third measurement device 54 apart from the first and second measurement devices 46, 48, if desired, and may track the amount of fuel gas stored and/or consumed by the vehicle and communicate this information to the filling system controller 18 at the beginning of a filling event so that an accurate gauge of Qstart can be accounted for during filling.
If ΔQ [Qtarget−(Qstart+Qnet)] is greater than zero, then the storage tank 12 has not been filled to the desired level. If ΔQ is less than or equal to zero, then the storage tank 12 is filled to the desired level. The controller 18 makes this determination at step 106 in the illustrated example. If the storage tank 12 is filled to the desired level (ΔQ≦0), then the controller 18 instructs the filling system 10 to stop filling the tank 12 (e.g., by closing a system valve, powering down a system compressor, opening a by-pass valve, etc.) as indicated at step 108. When ΔQ is greater than zero, which is the case for essentially the entire duration of the filling event, the controller 18 decides how to operate the fuel gas charging amplifier 16 at step 110. If the tank 12 is nearly full, within a tolerance band Qtol such that ΔQ<Qtol, the controller 18 does not change the operating parameters of the fuel gas charging amplifier 16 and returns to step 102 and continuously repeats steps 102, 104, 106 and 110 until ΔQ≦0 at step 106. When ΔQ is not within the tolerance band Qtol, the controller 18 operates to increase the gain of the fuel gas charging amplifier 16 at step 112 before returning to step 102 so that the tank 12 fills more quickly. As shown in
Step 112 may include a simple on-off operation of the fuel gas charging amplifier components. For instance, the compressor 42 and/or heat exchanger 44 may operate at respective maximum temperature-reducing capacities until the storage tank 12 is filled to the desired level. In other embodiments, the components 42, 44 of the fuel gas charging amplifier 16 may each operate within a range between zero and a maximum gain capacity.
The filling system 10 illustrated in
where
ΔQ equals [Qtarget−(Qstart+Qnet)] and Qnet equals dQnet/dt.
If the predicted fill time tp is greater than the target fill time (tp>ttarget) at step 116, the controller 18 operates to increase the gain of the fuel gas charging amplifier 16 at step 112. If the predicted fill time tp is less than the target fill time (tp<ttarget) at step 118, the controller 18 operates to decrease the gain of the fuel gas charging amplifier 16 at step 122. If the predicted fill time tp is equal to the target fill time (tp=ttarget) at step 120, the controller 18 continues to operate the fuel gas charging amplifier 16 in its current operational state. The respective increases and decreases in the gain of the fuel gas charging amplifier 16 may include on-off (increase-decrease) operation of the amplifier components and/or changes in their operating parameters, such as increased or decreased turbine speed in the compressor 42 or increased or decreased flow rate of a heat exchange coolant in the heat exchanger 44 for respective increases or decreases in gain.
The above description of preferred exemplary embodiments and related examples are merely descriptive in nature; they are not intended to limit the scope of the claims that follow. Each of the terms used in the appended claims should be given its ordinary and customary meaning unless specifically and unambiguously stated otherwise in the specification.
This application claims the benefit of U.S. provisional patent application No. 61/896,508 filed on Oct. 28, 2013, the entire contents of which are incorporated herein by reference.
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/US2014/062607 | 10/28/2014 | WO | 00 |
Number | Date | Country | |
---|---|---|---|
61896508 | Oct 2013 | US |