Apparatus and system for swing adsorption processes

Information

  • Patent Grant
  • 11857913
  • Patent Number
    11,857,913
  • Date Filed
    Tuesday, March 29, 2022
    2 years ago
  • Date Issued
    Tuesday, January 2, 2024
    4 months ago
Abstract
Provided are apparatus and systems for performing a swing adsorption process. This swing adsorption process may involve performing dampening for fluctuations in the streams conducted away from the adsorbent bed unit. The process may be utilized for swing adsorption processes, such as rapid cycle TSA and/or rapid cycle PSA, which are utilized to remove one or more contaminants from a gaseous feed stream.
Description
FIELD

The present techniques relate to a method and system associated with swing adsorption processes used in conditioning streams for downstream processing. In particular, the method and system involves performing swing adsorption processes to dampen the temperature swing in the product stream to within acceptable limits for the downstream process.


BACKGROUND

Gas separation is useful in many industries and can typically be accomplished by flowing a mixture of gases over an adsorbent material that preferentially adsorbs one or more gas components while not adsorbing one or more other gas components. The non-adsorbed components are recovered as a separate product.


One particular type of gas separation technology is swing adsorption, such as temperature swing adsorption (TSA), pressure swing adsorption (PSA), partial pressure swing adsorption (PPSA), rapid cycle temperature swing adsorption (RCTSA), rapid cycle pressure swing adsorption (RCPSA), rapid cycle partial pressure swing adsorption (RCPPSA), and not limited to but also combinations of the fore mentioned processes, such as pressure and temperature swing adsorption. As an example, PSA processes rely on the phenomenon of gases being more readily adsorbed within the pore structure or free volume of an adsorbent material when the gas is under pressure. That is, the higher the gas pressure, the greater the amount of readily-adsorbed gas adsorbed. When the pressure is reduced, the adsorbed component is released, or desorbed from the adsorbent material.


The swing adsorption processes (e.g., PSA and/or TSA) may be used to separate gases of a gas mixture because different gases tend to fill the micropore of the adsorbent material to different extents. For example, if a gas mixture, such as natural gas, is passed under pressure through a vessel containing an adsorbent material that is more selective towards carbon dioxide than it is for methane, at least a portion of the carbon dioxide is selectively adsorbed by the adsorbent material, and the gas exiting the vessel is enriched in methane. When the adsorbent material reaches the end of its capacity to adsorb carbon dioxide, it is regenerated by reducing the pressure, thereby releasing the adsorbed carbon dioxide. Then, the adsorbent material is typically purged and repressurized prior to starting another adsorption cycle.


The swing adsorption processes typically involve adsorbent bed units, which include adsorbent beds disposed within a housing and configured to maintain fluids at various pressures for different steps in a cycle within the unit. These adsorbent bed units utilize different packing material in the bed structures. For example, the adsorbent bed units utilize checker brick, pebble beds or other available packing. As an enhancement, some adsorbent bed units may utilize engineered packing within the bed structure. The engineered packing may include a material provided in a specific configuration, such as a honeycomb, ceramic forms or the like.


Further, various adsorbent bed units may be coupled together with conduits and valves to manage the flow of fluids through the cycle. Orchestrating these adsorbent bed units involves coordinating the steps in the cycle for each of the adsorbent bed units with other adsorbent bed units in the system. A complete cycle can vary from seconds to minutes as it transfers a plurality of gaseous streams through one or more of the adsorbent bed units.


A challenge with rapid cycle processes is the temperature, compositional, and pressure pulse associated with the transition of streams through the adsorbent beds between the various steps in a cycle. For example, swing adsorption processes for deep dehydration used with LNG applications, a temperature swing step may be used to regenerate a spent adsorbent bed after an adsorption step. However, this heating of the adsorbent bed may rely upon the feed stream to cool the adsorbent bed. As a result, the feed steam may cool the adsorbent bed during the initial portion of the adsorption step. As a result, the product stream from the adsorbent bed may involve temperature swings. These temperature fluctuations are problematic for the liquefaction process.


In addition to the temperature fluctuations, compositional variations may also be present from the swing adsorption processes. For example, the composition variation in purge gas leaving an adsorbent bed during regeneration. The concentration of the contaminant initially increases, as the adsorbent bed is being rapidly regenerated, before decreasing. Furthermore, the temperature of this gas stream gradually increases during the step. Certain downstream processes may need to have the composition variations and/or temperature fluctuations within specific levels to operate properly.


Accordingly, there remains a need in the industry for apparatus, methods, and systems that provided enhancements to managing temperature, compositional, and pressure pulses associated with hydrocarbon recovery processes. In particular, a need exists for enhancements to temperature, compositional, and pressure pulses in rapid cycle swing adsorption processes.


SUMMARY OF THE INVENTION

In one embodiment, a process for removing contaminants from a gaseous feed stream with a swing adsorption process is described. The process comprising: a) performing an adsorption step, wherein the adsorption step comprises passing a gaseous feed stream through an adsorbent bed unit to remove one or more contaminants and produce a product stream; b) interrupting the flow of the gaseous feed stream; c) performing a heating step, wherein the heating step comprises passing a heating stream through the adsorbent bed unit to remove one or more contaminants from the adsorbent bed unit; d) performing a cooling step, wherein the cooling step comprises lessening the temperature of an adsorbent material in the adsorbent bed unit by passing a cooling stream through the adsorbent bed unit; and e) repeating the steps a) to d) for at least one additional cycle in the swing adsorption process.


In one or more embodiments, the process includes one or more enhancements. The process may include wherein the cycle duration is for a period greater than 1 second and less than 600 seconds; wherein the gaseous feed stream is a hydrocarbon containing stream having greater than one volume percent hydrocarbons based on the total volume of the feed stream; wherein the gaseous feed stream comprises hydrocarbons and CO2, wherein the CO2 content is from about 200 parts per million volume to about 2% volume of the gaseous feed stream; wherein the swing adsorption process is configured to lower the carbon dioxide (CO2) level to less than 50 parts per million; passing the product stream to a downstream process; wherein the downstream process is a liquefied natural gas (LNG) process that comprises an LNG process unit; wherein the downstream process is a cryogenic natural gas liquefaction (NGL) process having a NGL process unit; wherein the cycle duration is greater than 2 seconds and less than 180 seconds; wherein the cooling stream is passed from the adsorbent bed unit to a conditioning unit; and the conditioned stream is passed from the conditioning unit to another adsorbent bed unit as the heating stream; wherein the heating stream is passed in a direction that is counter-current to the direction that the feed stream is passed; and the cooling stream is passed in a direction that is counter-current to the direction that the feed stream is passed; further comprising splitting a purge stream into the heating stream and the cooling stream; wherein the cooling stream is passed in a direction that is co-current to the direction that the feed stream is passed; and the heating stream is passed in a direction that is counter-current to the direction that the feed stream is passed; further comprising determining whether the product stream is within acceptable temperature limits; wherein the acceptable temperature limits include the product stream having temperatures within 50° F. of feed temperature of the gaseous feed stream; wherein the acceptable temperature limits include the product stream having temperatures within 25° F. of feed temperature of the gaseous feed stream; wherein the acceptable temperature limits include the product stream having temperatures within 10° F. of feed temperature of the gaseous feed stream; wherein the swing adsorption process is a rapid cycle temperature swing adsorption process; and/or wherein the swing adsorption process is a rapid cycle temperature swing adsorption process and a rapid cycle temperature swing adsorption process.


In another embodiment, a cyclical swing adsorption system is described. The system may comprise: a plurality of adsorbent bed units coupled to a plurality of manifolds, each of the adsorbent bed units is configured to pass different streams through the adsorbent bed unit between two or more steps in a swing adsorption cycle and each of the adsorbent bed units is configured to remove one or more contaminants from a feed stream to form a product stream and wherein each of the adsorbent bed units comprise: a housing; an adsorbent material disposed within the housing; a plurality of valves, wherein at least one of the plurality of valves is associated with one of the plurality of manifolds and is configured to manage fluid flow along a flow path extending between the respective manifold and the adsorbent material; and wherein the cyclical swing adsorption system is configured to dampen one or more of temperature, compositional, and pressure pulses associated with the transition of different streams through the adsorbent beds between the two or more steps in the swing adsorption cycle.


In one or more embodiments, the system includes one or more enhancements. The cyclical swing adsorption system may include wherein the plurality of manifolds comprise a feed manifold configured to pass the feed stream to the plurality of adsorbent bed units during an adsorption step, a product manifold configured to pass the product stream from the plurality of adsorbent bed units during the adsorption step, a purge manifold configured to pass a purge stream to the plurality of adsorbent bed units during a regeneration step, a purge product manifold configured to pass a purge product stream from the plurality of adsorbent bed units during the regeneration step, each manifold of the plurality of manifolds is associated with one swing adsorption process step of a plurality of swing adsorption process steps; wherein the plurality of manifolds comprise a cooling manifold configured to pass a cooling stream to the plurality of adsorbent bed units during a cooling step, a cooling product manifold configured to pass a cooling product stream from the plurality of adsorbent bed units during the cooling step; wherein the plurality of manifolds comprise a feed manifold configured to pass the feed stream to the plurality of adsorbent bed units during an adsorption step, a product manifold configured to pass the product stream from the plurality of adsorbent bed units during the adsorption step, a purge manifold configured to split the purge stream into a first purge stream configured to pass to the plurality of adsorbent bed units during a heating step and a second purge stream configured to pass to the plurality of adsorbent bed units during a cooling step, a first purge product manifold configured to pass a first purge product stream from the plurality of adsorbent bed units during the heating step, and a second purge product manifold configured to pass a second purge product stream from the plurality of adsorbent bed units during the cooling step; a heating unit disposed upstream of the split in the purge manifold, wherein the heating unit is configured to increase the temperature of the first purge stream prior to passing the plurality of adsorbent bed units during a heating step; wherein the plurality of manifolds comprise a feed manifold configured to pass the feed stream to the plurality of adsorbent bed units during an adsorption step, a product manifold configured to pass the product stream from the plurality of adsorbent bed units during the adsorption step, a purge manifold configured to pass a cooling stream to the plurality of adsorbent bed units during a cooling step and a cooling purge product manifold configured to pass a cooling purge product stream from the plurality of adsorbent bed units during the cooling step and configured to pass a heating stream to another of the plurality of adsorbent bed units during a heating step, and a second purge product manifold configured to pass a heating purge product stream from the plurality of adsorbent bed units during the heating step; a heating unit associated with the cooling purge product manifold and configured to heat the cooling purge product stream to form the heating stream; a liquefied natural gas (LNG) process that comprises an LNG process unit and is configured to receive the product stream; a cryogenic natural gas liquefaction (NGL) process having a NGL process unit and is configured to receive the product stream; a dampening system in fluid communication with the plurality of adsorbent bed units and configured to lessen one or more of temperature fluctuations, compositional fluctuations, and any combination thereof associated with the transition of the different streams through the adsorbent beds between the two or more steps in the swing adsorption cycle; wherein the dampening system comprises a heat exchanger configured to provide sufficient thermal capacitance to dampen temperature pulses in the product stream; wherein the dampening system comprises an accumulator configured to manage compositions of the product stream; wherein the dampening system comprises a mixing unit configured to manage compositions of the product stream; wherein the plurality of manifolds further comprise a blowdown manifold configured to pass a blowdown stream from the plurality of adsorbent bed units during a blowdown step; wherein the plurality of valves comprise one or more poppet valves; and/or wherein the plurality of adsorbent bed units are configured to operate at pressures between 0.1 bar absolute (bara) and 100 bara.





BRIEF DESCRIPTION OF THE FIGURES

The foregoing and other advantages of the present disclosure may become apparent upon reviewing the following detailed description and drawings of non-limiting examples of embodiments.



FIG. 1 is a three-dimensional diagram of the swing adsorption system with six adsorbent bed units and interconnecting piping in accordance with an embodiment of the present techniques.



FIG. 2 is a diagram of a portion of an adsorbent bed unit having associated valve assemblies and manifolds in accordance with an embodiment of the present techniques.



FIG. 3 is an exemplary flow chart for performing an external startup mode of a swing adsorption process in accordance with an embodiment of the present techniques.



FIG. 4 is an exemplary diagram of steps in a swing adsorption process in accordance with an embodiment of the present techniques.



FIG. 5 is another exemplary diagram of steps in a swing adsorption process in accordance with an embodiment of the present techniques.



FIG. 6 is an exemplary diagram of product gas temperature from a swing adsorption process.





DETAILED DESCRIPTION OF THE INVENTION

Unless otherwise explained, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure pertains. The singular terms “a,” “an,” and “the” include plural referents unless the context clearly indicates otherwise. Similarly, the word “or” is intended to include “and” unless the context clearly indicates otherwise. The term “includes” means “comprises.” All patents and publications mentioned herein are incorporated by reference in their entirety, unless otherwise indicated. In case of conflict as to the meaning of a term or phrase, the present specification, including explanations of terms, control. Directional terms, such as “upper,” “lower,” “top,” “bottom,” “front,” “back,” “vertical,” and “horizontal,” are used herein to express and clarify the relationship between various elements. It should be understood that such terms do not denote absolute orientation (e.g., a “vertical” component can become horizontal by rotating the device). The materials, methods, and examples recited herein are illustrative only and not intended to be limiting.


As used herein, “stream” refers to fluid (e.g., solids, liquid and/or gas) being conducted through various equipment. The equipment may include conduits, vessels, manifolds, units or other suitable devices.


As used herein, “conduit” refers to a tubular member forming a channel through which something is conveyed. The conduit may include one or more of a pipe, a manifold, a tube or the like.


The provided processes, apparatus, and systems of the present techniques may be used in swing adsorption processes that remove contaminants (CO2, H2O, and H2S) from feed streams, such as hydrocarbon containing streams. As may be appreciated and as noted above, the hydrocarbon containing feed streams may have different compositions. For example, hydrocarbon feed streams vary widely in amount of acid gas, such as from several parts per million acid gas to 90 volume percent (vol. %) acid gas. Non-limiting examples of acid gas concentrations from exemplary gas reserves sources include concentrations of approximately: (a) 4 ppm H2S, 2 vol. % CO2, 100 ppm H2O (b) 4 ppm H2S, 0.5 vol. % CO2, 200 ppm H2O (c) 1 vol. % H2S, 2 vol. % CO2, 150 ppm H2O, (d) 4 ppm H2S, 2 vol. % CO2, 500 ppm H2O, and (e) 1 vol. % H2S, 5 vol. % CO2, 500 ppm H2O. Further, in certain applications the hydrocarbon containing stream may include predominately hydrocarbons with specific amounts of CO2 and/or water. The gaseous feed stream utilized in the processes herein comprises, or consists essentially of, a hydrocarbon containing stream. For example, the gaseous feed stream may have greater than 0.00005 volume percent CO2 based on the total volume of the gaseous feed stream and less than 2 volume percent CO2 based on the total volume of the gaseous feed stream; or less than 10 volume percent CO2 based on the total volume of the gaseous feed stream. In other embodiments, the gaseous feed stream may have a CO2 content from about 200 parts per million volume to about 2% volume based on the gaseous feed stream. The processing of feed streams may be more problematic when certain specifications have to be satisfied.


The removal of contaminants may be performed by swing adsorption processes to prepare the stream for further downstream processing, such as NGL processing and/or LNG processing. For example, natural gas feed streams for liquefied natural gas (LNG) applications have stringent specifications on the CO2 content to ensure against formation of solid CO2 at cryogenic temperatures. The LNG specifications may involve the CO2 content to be less than or equal to 50 ppm. Such specifications are not applied on natural gas streams in pipeline networks, which may involve the CO2 content up to 2 vol. % based on the total volume of the gaseous feed stream. As such, for LNG facilities that use the pipeline gas (e.g., natural gas) as the raw feed, additional treating or processing steps are utilized to further purify the stream. Further, the present techniques may be used to lower the water content of the stream to less than 0.1 ppm. Exemplary swing adsorption processes and configurations may include U.S. Patent Application Publication Nos. US2017/0056814, US2017/0113175 and US2017/0113173, and U.S. Pat. Nos. 10,080,991, 10,124,286, 10,080,992 and 10,040,022, which are each incorporated by reference herein.


The present techniques provide configurations and processes that are utilized to enhance swing adsorption processes. As noted above, rapid cycle pressure and temperature swing adsorption processes may be used to dehydrate streams and/or remove low-level CO2. To manage the temperature, compositional, and pressure pulses associated with the transition of streams within the adsorbent beds between the steps in the cycle, the present techniques may include additional steps or mechanisms. The present techniques provide a method to minimize the temperature and/or compositional fluctuations in a stream being conducted away from the rapid cycle swing adsorption process. In other configurations, a system is used to minimize the temperature and/or compositional fluctuations in one or more streams being conducted away from the rapid cycle swing adsorption process units.


For example, one configuration may include using a dampening system, which is disposed downstream of the swing adsorption bed units and upstream of the downstream processing units, such as a LNG processing unit. The dampening system may be configured to dampen the respective fluctuations. By way of example, the dampening system may include a heat exchanger and/or a piping network that may be used to provide sufficient thermal mass to provide the thermal capacitance to dampen any associated temperature pulses in the product stream.


In yet another example, the dampening system may include an accumulator may be used to manage the composition of the stream being conducted away from the adsorbent bed unit. The accumulator may be disposed downstream of the swing adsorption bed units and upstream of the downstream processing units, such as a LNG processing unit. As a specific example, the purge gas being conducted away from the adsorbent bed that is used in the regeneration step. The concentration of the contaminants in the purge product stream may initially be higher and then decrease during the later portion of the purge step. The accumulator may be used to mix or intermingle the purge product stream to manage the composition into a more uniform distribution of contaminants. Furthermore, the dampening system may include a heat exchanger and an accumulator. The temperature of the purge gas stream may gradually increases during the purge step. If the purge stream is to be provided to a downstream system, such as a gas turbine, the dampening system may manage the pulses to provide that the gas wobbe index is within acceptable limits.


In another configuration, the swing adsorption process may include a cooling step to manage the temperature of the adsorbent bed and resulting product stream. The cooling step may adjust the temperature (e.g., cool) the adsorbent bed down after a regeneration step. As such, the product stream being conducted away from the adsorbent bed unit may be at a temperature within acceptable limits. For example, in an LNG dehydration system, a cooling step may be used after the regeneration step (e.g., a temperature swing step), which may be used to regenerate a spent adsorbent bed. By using the cooling step, the feed stream may not be relied upon to adjust the temperature of the adsorbent bed during the swing adsorption cycle because the cooling step may be used to dampen the temperature fluctuations of the resulting product stream from the adsorbent bed unit. As a result of the cooling step, the product gas temperature of the product stream may be managed within a temperature threshold that may enhance the downstream processing of the product stream. Accordingly, the product stream may be passed to the liquefaction process within acceptable temperature limits. By way of example, the acceptable temperature limits may include product streams for the swing adsorption system having temperatures within 50° F. of feed temperature for the swing adsorption system, within 25° F. of feed temperature for the swing adsorption system, or within 10° F. of feed temperature for the swing adsorption system.


By way of example, conventional processes, such as molecular sieve processes, regenerate a spent molecular sieve bed by heating the bed to remove contaminants followed by cooling the molecular sieve bed to prepare the molecular sieve bed for adsorption. These steps are usually done by the same regeneration gas stream that is initially heated to heat the molecular sieve bed and later not heated to cool the molecular sieve bed. In such a configuration, the heating and cooling steps are not continuous (e.g., at least one bed is being cooled and one bed is being heated simultaneously at any instant).


For LNG applications, the purge gas stream may be sourced from end-flash compression, boil-off-gas compression, directly from the feed gas or a combination thereof. The purge stream may serve as the fuel gas stream and is limited in flow rate. To use the same stream for cooling and heating, two configurations may be utilized. The first configuration may splits the available purge stream into a cool stream and a heating for different adsorbent beds. While no recycling is performed, the cooling and heating are performed continuously (e.g., at least one adsorbent bed is being cooled and one bed is being heated at any instant). If the available flow rate is not sufficient, then the stream may be recycled. However, the stream may be recycled, such that the heating stream remains contaminant free (e.g., during the cooling step contaminants from the adsorbent bed do not move into the purge stream because of the flow direction being co-current to the feed flow direction). These steps are continuous, which is beneficial for RCPSA and/or RCPSTA cycles ensuring steady flows through various streams. The recycling provides a few additional aspects, such as a method to simultaneously control the product temperature and recover heat internally (e.g., reduced overall heat required to regenerate the bed).


In yet another configuration, the present techniques may utilize a cooling step in the swing adsorption process. The purge gas stream, which may be at or near ambient temperatures, may be split into two streams. The first stream may be heated and used to regenerate the adsorbent bed, while the second stream may be used to cool a recently regenerated adsorbent bed. The first and second streams may be introduced in a counter-current direction relative to the feed stream, which may performed to maintain the dryness of the product end of the adsorbent bed throughout the regeneration and cooling steps of the swing adsorption cycle.


Further, in another configuration, the present techniques may utilize a different cooling step in the swing adsorption process. In this configuration, the purge stream, which may be at or near ambient temperatures, is first passed in a co-current direction relative to the direction of the feed stream to cool a recently regenerated adsorbent bed. The cooling step may lessen the temperature of the adsorbent bed, while recovering some of the heat in the adsorbent bed. The resulting gas stream is then heated and introduced to a spent adsorbent bed to regenerate the adsorbent bed. This configuration has the additional benefit of recovering some of the heat from the regeneration step of the swing adsorption cycle.


In still yet another configuration, additional dampening may be achieved by operating multiple adsorbent beds out of sequence on feed. For example, a new adsorbent bed may be introduced on the feed stream, while a different adsorbent bed is already operational and producing product at nearly the feed temperature.


In other configurations, the present techniques may involve temperature swing dampening. The method of managing the temperature fluctuations and/or compositional fluctuations in the purge gas stream may use a combination of heat exchangers and mixing drums. The heat exchangers may provide a method to cool the gas stream to a specific temperature range. As the purge stream may be a small flow rate in comparison the product stream, the size of the heat exchanger may be relatively small. Furthermore, in performing dehydration, the heat exchanger may be used to condense excess water in the purge stream. The mixing drum provides the proper residence time to manage the compositional pulses, such that the gas stream leaving the mixing drum is more uniform in composition.


The present techniques may be a swing adsorption process, and specifically a rapid cycle adsorption process. The present techniques may include some additional equipment, such as one or more conduits and/or one or more manifolds that provide a fluid path for the cooling step and/or dampening system. In addition, other components and configurations may be utilized to provide the swing adsorption process, such as rapid cycle enabling hardware components (e.g., parallel channel adsorbent bed designs, rapid actuating valves, adsorbent bed configurations that integrate with other processes). Exemplary swing adsorption processes and configurations may include U.S. Patent Application Publication Nos. US2017/0056814, US2017/0113175 and US2017/0113173, and U.S. Pat. Nos. 10,080,991, 10,124,286, 10,080,992 and 10,040,022, which are each incorporated by reference herein.


In one or more configurations, a swing adsorption process may include performing various steps. For the example, the present techniques may be used to remove contaminants from a gaseous feed stream with a swing adsorption process, which may be utilized with one or more downstream processes. The process comprising: a) performing a heating step, wherein the heating step comprises passing a heating stream through the adsorbent bed unit to remove one or more contaminants from the adsorbent bed unit (e.g., a heated purge step that comprises passing a heated purge stream through an adsorbent bed unit to remove contaminants from an adsorbent bed within a housing of the adsorbent bed unit to form a purge product stream, which may be a heated purge stream); b) performing a cooling step, wherein the cooling step may comprise passing cooling stream through an adsorbent bed unit to remove lessen the temperature of the adsorbent bed within a housing of the adsorbent bed unit to lessen the temperature of the adsorbent bed prior to the one or more adsorption steps; c) performing one or more adsorption steps, wherein each of the one or more adsorption steps comprise passing a gaseous feed stream through an adsorbent bed unit having an adsorbent bed to separate contaminants from the gaseous feed stream to form a product stream. In addition, the method may include determining whether the product stream and/or purge stream is within a temperature specification and/or composition specification; d) if the product stream and/or purge stream is within the respective specification (e.g., is below a certain threshold), passing the product stream to a downstream process; and e) if the product stream is not within the specification (e.g., above a certain threshold), passing the product stream and/or purge stream through the dampening system.


In other certain embodiments, the swing adsorption process may be integrated with downstream equipment and processes. The downstream equipment and processes may include control freeze zone (CFZ) applications, niotrogen removal unit (NRU), cryogenic NGL recovery applications, LNG applications, and other such applications. Each of these different applications may include different specifications for the feed stream in the respective process. For example, a cryogenic NGL process or an LNG process and may be integrated with the respective downstream equipment. As another example, the process may involve H2O and/or CO2 removal upstream of a cryogenic NGL process or the LNG process and may be integrated with respective downstream equipment.


In certain configurations, the system utilizes a combined swing adsorption process, which combines TSA and PSA, for treating of pipeline quality natural gas to remove contaminants for the stream to satisfy LNG specifications. The swing adsorption process, which may be a rapid cycle process, is used to treat natural gas that is at pipeline specifications (e.g., a feed stream of predominately hydrocarbons along with less than or equal to about 2% volume CO2 and/or less than or equal to 4 ppm H2S) to form a stream satisfying the LNG specifications (e.g., less than 50 ppm CO2 and less than about 4 ppm H2S). The product stream, which may be the LNG feed stream, may have greater than 98 volume percent hydrocarbons based on the total volume of the product stream, while the CO2 and water content are below certain thresholds. The LNG specifications and cryogenic NGL specifications may involve the CO2 content to be less than or equal to 50 ppm, while the water content of the stream may be less than 0.1 ppm.


Moreover, the present techniques may include a specific process flow to remove contaminants, such as CO2 and/or water. For example, the process may include an adsorbent step and a regeneration step, which form the cycle. The adsorbent step may include passing a gaseous feed stream at a feed pressure and feed temperature through an adsorbent bed unit to separate one or more contaminants from the gaseous feed stream to form a product stream. The feed stream may be passed through the adsorbent bed in a forward direction (e.g., from the feed end of the adsorbent bed to the product end of the adsorbent bed). Then, the flow of the gaseous feed stream may be interrupted for a regeneration step. The regeneration step may include one or more depressurization steps, one or more heating steps, and/or one or more purge steps. The depressurization steps, which may be or include a blowdown step, may include reducing the pressure of the adsorbent bed unit by a predetermined amount for each successive depressurization step, which may be a single step and/or multiple steps. The depressurization step may be provided in a forward direction or may preferably be provided in a countercurrent direction (e.g., from the product end of the adsorbent bed to the feed end of the adsorbent bed). The heating step may include passing a heating stream into the adsorbent bed unit, which may be a recycled stream through the heating loop and is used to heat the adsorbent material. The purge step may include passing a purge stream into the adsorbent bed unit, which may be a once through purge step and the purge stream may be provided in countercurrent flow relative to the feed stream. The purge stream may be provided at a purge temperature and purge pressure, which may include the purge temperature and purge pressure being similar to the heating temperature and heating pressure used in the heating step. Then, the cycle may be repeated for additional streams. Additionally, the process may include one or more re-pressurization steps after the purge step and prior to the adsorption step. The one or more re-pressurization steps may be performed, wherein the pressure within the adsorbent bed unit is increased with each re-pressurization step by a predetermined amount with each successive re-pressurization step. The cycle duration may be for a period greater than 1 second and less than 600 seconds, for a period greater than 2 second and less than 300 seconds, for a period greater than 2 second and less than 180 seconds, for a period greater than 5 second and less than 150 seconds or for a period greater than 5 second and less than 90 seconds.


In one or more embodiments, the present techniques can be used for any type of swing adsorption process. Non-limiting swing adsorption processes for which the present techniques may be used include pressure swing adsorption (PSA), vacuum pressure swing adsorption (VPSA), temperature swing adsorption (TSA), partial pressure swing adsorption (PPSA), rapid cycle pressure swing adsorption (RCPSA), rapid cycle thermal swing adsorption (RCTSA), rapid cycle partial pressure swing adsorption (RCPPSA), as well as combinations of these processes. For example, the preferred swing adsorption process may include a combined pressure swing adsorption and temperature swing adsorption, which may be performed as a rapid cycle process. Exemplary swing adsorption processes and configurations may include U.S. Patent Application Publication Nos. US2017/0056814, US2017/0113175 and US2017/0113173, and U.S. Pat. Nos. 10,080,991, 10,124,286, 10,080,992, 10,040,022, 7,959,720, 8,545,602, 8,529,663, 8,444,750, 8,529,662 and 9,358,493, which are each herein incorporated by reference in their entirety.


Further still, in one or more configurations, a variety of adsorbent materials may be used to provide the mechanism for the separations. Examples include zeolite 3A, 4A, 5A, ZK4 and MOF-74. However, the process is not limited to these adsorbent materials, and others may be used as well.


In one configuration, a process for removing contaminants from a gaseous feed stream with a swing adsorption process is described. The process may comprise: a) performing an adsorption step, wherein the adsorption step comprises passing a gaseous feed stream through an adsorbent bed unit to remove one or more contaminants and produce a product stream; b) interrupting the flow of the gaseous feed stream; c) performing a heating step, wherein the heating step comprises passing a heating stream through the adsorbent bed unit to remove one or more contaminants from the adsorbent bed unit; d) performing a cooling step, wherein the cooling step comprises lessening the temperature of an adsorbent material in the adsorbent bed unit by passing a cooling stream through the adsorbent bed unit; and e) repeating the steps a) to d) for at least one additional cycle in the swing adsorption process.


In one or more configurations, the process may include one or more enhancements. The process may include wherein the cycle duration is for a period greater than 1 second and less than 600 seconds; wherein the gaseous feed stream is a hydrocarbon containing stream having greater than one volume percent hydrocarbons based on the total volume of the feed stream; wherein the gaseous feed stream comprises hydrocarbons and CO2, wherein the CO2 content is in the range of two hundred parts per million volume and less than or equal to about 2% volume of the gaseous feed stream; wherein the swing adsorption process is configured to lower the carbon dioxide (CO2) level to less than 50 parts per million; passing the product stream to a downstream process; wherein the downstream process is a liquefied natural gas (LNG) process that comprises an LNG process unit; wherein the downstream process is a cryogenic natural gas liquefaction (NGL) process having a NGL process unit; wherein the cycle duration is greater than 2 seconds and less than 180 seconds; wherein the cooling stream is passed from the adsorbent bed unit to a conditioning unit; and the conditioned stream is passed from the conditioning unit to another adsorbent bed unit as the heating stream; wherein the heating stream is passed in a direction that is counter-current to the direction that the feed stream is passed; and the cooling stream is passed in a direction that is counter-current to the direction that the feed stream is passed; further comprising splitting a purge stream into the heating stream and the cooling stream; wherein the cooling stream is passed in a direction that is co-current to the direction that the feed stream is passed; and the heating stream is passed in a direction that is counter-current to the direction that the feed stream is passed; further comprising determining whether the product stream is within acceptable temperature limits; wherein the acceptable temperature limits include the product stream having temperatures within 50° F. of feed temperature of the gaseous feed stream; wherein the acceptable temperature limits include the product stream having temperatures within 25° F. of feed temperature of the gaseous feed stream; wherein the acceptable temperature limits include the product stream having temperatures within 10° F. of feed temperature of the gaseous feed stream; wherein the swing adsorption process is a rapid cycle temperature swing adsorption process; and/or wherein the swing adsorption process is a rapid cycle temperature swing adsorption process and a rapid cycle temperature swing adsorption process.


In another configuration, a cyclical swing adsorption system is described. The system may comprise: a plurality of adsorbent bed units coupled to a plurality of manifolds, each of the adsorbent bed units is configured to pass different streams through the adsorbent bed unit between two or more steps in a swing adsorption cycle and each of the adsorbent bed units is configured to remove one or more contaminants from a feed stream to form a product stream and wherein each of the adsorbent bed units comprise: a housing; an adsorbent material disposed within the housing; a plurality of valves, wherein at least one of the plurality of valves is associated with one of the plurality of manifolds and is configured to manage fluid flow along a flow path extending between the respective manifold and the adsorbent material; and wherein the cyclical swing adsorption system is configured to dampen one or more of temperature, compositional, and pressure pulses associated with the transition of different streams through the adsorbent beds between the two or more steps in the swing adsorption cycle.


In one or more configurations, the system may include one or more enhancements. The cyclical swing adsorption system may include wherein the plurality of manifolds comprise a feed manifold configured to pass the feed stream to the plurality of adsorbent bed units during an adsorption step, a product manifold configured to pass the product stream from the plurality of adsorbent bed units during the adsorption step, a purge manifold configured to pass a purge stream to the plurality of adsorbent bed units during a regeneration step, a purge product manifold configured to pass a purge product stream from the plurality of adsorbent bed units during the regeneration step, each manifold of the plurality of manifolds is associated with one swing adsorption process step of a plurality of swing adsorption process steps; wherein the plurality of manifolds comprise a cooling manifold configured to pass a cooling stream to the plurality of adsorbent bed units during a cooling step, a cooling product manifold configured to pass a cooling product stream from the plurality of adsorbent bed units during the cooling step; wherein the plurality of manifolds comprise a feed manifold configured to pass the feed stream to the plurality of adsorbent bed units during an adsorption step, a product manifold configured to pass the product stream from the plurality of adsorbent bed units during the adsorption step, a purge manifold configured to split the purge stream into a first purge stream configured to pass to the plurality of adsorbent bed units during a heating step and a second purge stream configured to pass to the plurality of adsorbent bed units during a cooling step, a first purge product manifold configured to pass a first purge product stream from the plurality of adsorbent bed units during the heating step, and a second purge product manifold configured to pass a second purge product stream from the plurality of adsorbent bed units during the cooling step; a heating unit disposed upstream of the split in the purge manifold, wherein the heating unit is configured to increase the temperature of the first purge stream prior to passing the plurality of adsorbent bed units during a heating step; wherein the plurality of manifolds comprise a feed manifold configured to pass the feed stream to the plurality of adsorbent bed units during an adsorption step, a product manifold configured to pass the product stream from the plurality of adsorbent bed units during the adsorption step, a purge manifold configured to pass a cooling stream to the plurality of adsorbent bed units during a cooling step and a cooling purge product manifold configured to pass a cooling purge product stream from the plurality of adsorbent bed units during the cooling step and configured to pass a heating stream to another of the plurality of adsorbent bed units during a heating step, and a second purge product manifold configured to pass a heating purge product stream from the plurality of adsorbent bed units during the heating step; a heating unit associated with the cooling purge product manifold and configured to heat the cooling purge product stream to form the heating stream; a liquefied natural gas (LNG) process that comprises an LNG process unit and is configured to receive the product stream; a cryogenic natural gas liquefaction (NGL) process having a NGL process unit and is configured to receive the product stream; a dampening system in fluid communication with the plurality of adsorbent bed units and configured to lessen one or more of temperature fluctuations, compositional fluctuations, and any combination thereof associated with the transition of the different streams through the adsorbent beds between the two or more steps in the swing adsorption cycle; wherein the dampening system comprises a heat exchanger configured to provide sufficient thermal capacitance to dampen temperature pulses in the product stream; wherein the dampening system comprises an accumulator configured to manage compositions of the product stream; wherein the dampening system comprises a mixing unit configured to manage compositions of the product stream; wherein the plurality of manifolds further comprise a blowdown manifold configured to pass a blowdown stream from the plurality of adsorbent bed units during a blowdown step; wherein the plurality of valves comprise one or more poppet valves; and/or wherein the plurality of adsorbent bed units are configured to operate at pressures between 0.1 bar absolute (bara) and 100 bara. The present techniques may be further understood with reference to the FIGS. 1 to 6 below.



FIG. 1 is a three-dimensional diagram of the swing adsorption system 100 having six adsorbent bed units and interconnecting piping. While this configuration is a specific example, the present techniques broadly relate to adsorbent bed units that can be deployed in a symmetrical orientation, or non-symmetrical orientation and/or combination of a plurality of hardware skids. Further, this specific configuration is for exemplary purposes as other configurations may include different numbers of adsorbent bed units.


In this system, the adsorbent bed units, such as adsorbent bed unit 102, may be configured for a cyclical swing adsorption process for removing contaminants from feed streams (e.g., fluids, gaseous or liquids). For example, the adsorbent bed unit 102 may include various conduits (e.g., conduit 104) for managing the flow of fluids through, to or from the adsorbent bed within the adsorbent bed unit 102. These conduits from the adsorbent bed units 102 may be coupled to a manifold (e.g., manifold 106) to distribute the flow to, from or between components. The adsorbent bed within an adsorbent bed unit may separate one or more contaminants from the feed stream to form a product stream. As may be appreciated, the adsorbent bed units may include other conduits to control other fluid steams as part of the process, such as purge streams, depressurizations streams, and the like. In particular, the adsorbent bed units may include startup mode equipment, such as one or more heating units (not shown), one or more external gas source manifolds, which may be one of the manifolds 106) and one or more expanders, as noted further below, which is used as part of the startup mode for the adsorbent beds. Further, the adsorbent bed unit may also include one or more equalization vessels, such as equalization vessel 108, which are dedicated to the adsorbent bed unit and may be dedicated to one or more step in the swing adsorption process. The equalization vessel 108 may be used to store the external stream, such as nitrogen for use in the startup mode cycle.


As an example, which is discussed further below in FIG. 2, the adsorbent bed unit 102 may include a housing, which may include a head portion and other body portions, that forms a substantially gas impermeable partition, an adsorbent bed disposed within the housing and a plurality of valves (e.g., poppet valves) providing fluid flow passages through openings in the housing between the interior region of the housing and locations external to the interior region of the housing. Each of the poppet valves may include a disk element that is seatable within the head or a disk element that is seatable within a separate valve seat inserted within the head (not shown). The configuration of the poppet valves may be any variety of valve at patterns or configuration of types of poppet valves. As an example, the adsorbent bed unit may include one or more poppet valves, each in flow communication with a different conduit associated with different streams. The poppet valves may provide fluid communication between the adsorbent bed and one of the respective conduits, manifolds or headers. The term “in direct flow communication” or “in direct fluid communication” means in direct flow communication without intervening valves or other closure means for obstructing flow. As may be appreciated, other variations may also be envisioned within the scope of the present techniques.


The adsorbent bed comprises a solid adsorbent material capable of adsorbing one or more components from the feed stream. Such solid adsorbent materials are selected to be durable against the physical and chemical conditions within the adsorbent bed unit 102 and can include metallic, ceramic, or other materials, depending on the adsorption process. Further examples of adsorbent materials are noted further below.



FIG. 2 is a diagram of a portion of an adsorbent bed unit 200 having valve assemblies and manifolds in accordance with an embodiment of the present techniques. The portion of the adsorbent bed unit 200, which may be a portion of the adsorbent bed unit 102 of FIG. 1, includes a housing or body, which may include a cylindrical wall 214 and cylindrical insulation layer 216 along with an upper head 218 and a lower head 220. An adsorbent bed 210 is disposed between an upper head 218 and a lower head 220 and the insulation layer 216, resulting in an upper open zone, and lower open zone, which open zones are comprised substantially of open flow path volume. Such open flow path volume in adsorbent bed unit contains gas that has to be managed for the various steps. The housing may be configured to maintain a pressure from 0 bara (bar absolute) to 150 bara within the interior region.


The upper head 218 and lower head 220 contain openings in which valve structures can be inserted, such as valve assemblies 222 to 240, respectively (e.g., poppet valves). The upper or lower open flow path volume between the respective head 218 or 220 and adsorbent bed 210 can also contain distribution lines (not shown) which directly introduce fluids into the adsorbent bed 210. The upper head 218 contains various openings (not show) to provide flow passages through the inlet manifolds 242 and 244 and the outlet manifolds 248, 250 and 252, while the lower head 220 contains various openings (not shown) to provide flow passages through the inlet manifold 254 and the outlet manifolds 256, 258 and 260. Disposed in fluid communication with the respective manifolds 242 to 260 are the valve assemblies 222 to 240. If the valve assemblies 222 to 240 are poppet valves, each may include a disk element connected to a stem element which can be positioned within a bushing or valve guide. The stem element may be connected to an actuating means, such as actuating means (not shown), which is configured to have the respective valve impart linear motion to the respective stem. As may be appreciated, the actuating means may be operated independently for different steps in the process to activate a single valve or a single actuating means may be utilized to control two or more valves. Further, while the openings may be substantially similar in size, the openings and inlet valves for inlet manifolds may have a smaller diameter than those for outlet manifolds, given that the gas volumes passing through the inlets may tend to be lower than product volumes passing through the outlets.


In swing adsorption processes, the cycle involves two or more steps that each has a certain time interval, which are summed together to be the cycle time or cycle duration. These steps include regeneration of the adsorbent bed following the adsorption step using a variety of methods including pressure swing, vacuum swing, temperature swing, purging (via any suitable type of purge fluid for the process), and combinations thereof. As an example, a PSA cycle may include the steps of adsorption, depressurization, purging, and re-pressurization. When performing the separation at high pressure, depressurization and re-pressurization (which may be referred to as equalization) may be performed in multiple steps to reduce the pressure change for each step and enhance efficiency. In some swing adsorption processes, such as rapid cycle swing adsorption processes, a substantial portion of the total cycle time is involved in the regeneration of the adsorbent bed. Accordingly, any reductions in the amount of time for regeneration results in a reduction of the total cycle time. This reduction may also reduce the overall size of the swing adsorption system.


Further, one or more of the manifolds and associated valves may be utilized as a dedicated flow path for one or more streams. For example, during the adsorption or feed step, the manifold 242 and valve assembly 222 may be utilized to pass the feed gas stream to the adsorbent bed 210, while the valve assembly 236 and manifold 256 may be used to conduct away the product stream from the adsorbent bed 210. During the regeneration or purge step, the manifold 244 and valve assembly 224 may be utilized to pass the purge or heating stream to the adsorbent bed 210, while the valve assembly 236 and manifold 256 may be used to conduct away the purge product stream from the adsorbent bed 210. Further, the manifold 254 and valve assembly 232 may be utilized for a cooling stream, while the valve assembly 230 and manifold 252 may be used to conduct away the cooling product stream from the adsorbent bed 210. As may be appreciated, the purge stream and/or cooling stream may be configured to flow counter current to the feed stream in certain embodiments.


Alternatively, the swing adsorption process may involve sharing one or more of the manifolds and associated valves. Beneficially, this configuration may be utilized to lessen any additional valves or connections for startup mode for adsorbent bed unit configurations that are subject to space limitations on the respective heads.


As noted above, the present techniques include various procedures that may be utilized for the swing adsorption process. The present techniques may include additional steps or mechanisms to manage the temperature, compositional, and pressure pulses associated with the transition of streams within the adsorbent beds between the steps in the cycle. The present techniques may include including a cooling step to minimize the temperature fluctuations in a stream being conducted away from the rapid cycle swing adsorption process. In other configurations, a system may include a dampening system that may be used to minimize the temperature fluctuations and/or compositional fluctuations in one or more streams being conducted away from the rapid cycle swing adsorption process units.


As an example, FIG. 3 is an exemplary flow chart for performing a swing adsorption process in accordance with an embodiment of the present techniques. In this flow chart 300, the swing adsorption process may remove one or more contaminants and may be used to manage the temperature fluctuations and/or compositional fluctuations in one or more streams being conducted away from the rapid cycle swing adsorption process units. For each of the adsorbent bed units, the swing adsorption process involves performing various steps, as shown in blocks 302 to 306, which is described as being performed for a single adsorbent bed unit for simplicity. Then, the streams from the adsorbent bed units may be used with the downstream equipment, as shown in blocks 308 to 314.


The process begins by performing the swing adsorption process for the adsorbent bed units, as shown in blocks 302 to 306. At block 302, an adsorption step is performed for the adsorbent bed. The adsorption step may include passing a gaseous feed stream through the adsorbent bed to remove one or more contaminants from the gaseous feed stream and to create a product stream that is conducted away from the adsorbent bed unit. At block 304, a heating step is performed for the adsorbent bed. The heating step, which may be one or more purge steps may include passing the purge stream through the adsorbent bed to create a purge product stream that is conducted away from the adsorbent bed unit. The product purge stream may include the external stream and a portion of the contaminants within the adsorbent bed. The product purge stream may be intermingled with a fuel gas stream and may be used in a turbine. Further, the purge stream may be subjected to a heating step prior to being passed to the adsorbent bed. The heating step may heat the external stream to a temperature less than 550° F., less than 500° F., less than 450° F. or less than 350° F., and may be greater than 50° F. of the gaseous feed stream temperature, greater than 100° F. of the gaseous feed stream temperature or greater than 250° F. of the gaseous feed stream temperature. For example, the purge stream used during the purge step may be a temperature in the range between 500° F. and greater than 50° F. of the gaseous feed stream temperature, in the range between 450° F. and greater than 100° F. of the gaseous feed stream temperature or 400° F. and greater than 200° F. of the gaseous feed stream temperature. The heating of the purge stream may include passing the purge stream through a heat exchanger or similar heating unit to increase the temperature of the purge stream. At block 306, the cooling step may optionally be performed with the adsorbent bed. The cooling step may include passing a stream of gas to cool the adsorbent bed. The cooling step may include which may be a recycled stream that passes through heat exchangers or a refrigeration system to conduct away heat from the recycled stream. The process may repeat the step 302 to 306 for another swing adsorption cycle.


After being processed, the streams from the adsorbent bed units may be used with the downstream equipment, as shown in blocks 308 to 314. At block 308, the product stream may optionally be measured. The product stream may be measured by a temperature sensor and/or a gas chromatograph or using another gas component analysis equipment. The product stream may also be measured by taking samples, using a moisture analyzer. Then, at block 310, a determination may be made whether the product stream is within the respective specification. The determination may include analyzing the product stream to determine the level of one or more of the temperature, pressure, composition and any combination thereof. If the product stream is within specification (e.g., contaminants are at or below a specific threshold), the product stream may be passed to downstream process, as shown in block 314. However, if the product stream is not within specifications, the product stream may be passed to the dampening system, as shown in block 312. The dampening system may include a heat exchanger, conduits, an accumulator and/or a mixing unit. The downstream processes may include a CFZ process, a cryogenic NGL recovery process, or an LNG process, with the associated equipment for each.


By way of example, the present techniques may include additional steps or mechanisms to manage the temperature, compositional, and pressure pulses associated with the transition of streams within the adsorbent beds between the steps in the swing adsorption cycle. In particular, the method may be used to minimize the temperature and/or compositional fluctuations in a stream through the use of cooling steps in the rapid cycle swing adsorption process, which is shown in FIGS. 4 to 6.



FIG. 4 is an exemplary diagram of a swing adsorption system 400 in accordance with an embodiment of the present techniques. In this configuration, a cooling step is used to manage the fluctuations in the streams from the swing adsorption system 400. In the swing adsorption system 400, a first adsorbent bed 404 is shown performing an adsorption step with the feed stream in a feed conduit 402 that is passed through the first adsorbent bed 404 and conducting a product stream away from the first adsorbent bed 404 via product conduit 406. A second adsorbent bed 410 is shown performing a cooling step with the cooling stream in a purge conduit 408 that is passed through the second adsorbent bed 410 and conducting a cooling product stream away from the second adsorbent bed 410 via product conduit 412. A third adsorbent bed 416 is shown performing a heating step or regeneration step with the purge stream in the purge conduit 408 that is passed through a heating unit 414 and then to the third adsorbent bed 416 and conducting a purge product stream away from the third adsorbent bed 416 via the product conduit 412. A fourth adsorbent bed 418 is shown in a stand-by with no streams being passed through the fourth adsorbent bed 418.


In this configuration, the purge stream (which may near the ambient temperatures) is split into two different streams. The first stream is heated in the heating unit 414 and used to regenerate a spent third adsorbent bed 416, while the second stream is used to cool a recently regenerated adsorbent bed 410. These streams may be introduced in a counter-current direction to the feed stream which maintains the dryness of the product end of the adsorbent bed throughout the regeneration step and cooling step. In this configuration, the cooling stream may not be recycled back to the swing adsorbent system be used as a purge stream. To regenerate an adsorption bed, the purge stream is largely devoid of the contaminant being removed. The cooling stream may contain a significant amount contaminant. As such, it cannot be recycled as a purge stream. The cooling step may be part of the overall regeneration process, such that a larger amount of contaminant is removed, while purging in this regeneration step and a smaller (but not insignificant) amount of contaminant is removed, while purging in the cooling step.



FIG. 5 is an exemplary diagram of a swing adsorption system 500 in accordance with an embodiment of the present techniques. In this configuration, a different cooling step is used to manage the fluctuations in the streams from the swing adsorption system 500. In the swing adsorption system 500, a first adsorbent bed 504 is shown performing an adsorption step with the feed stream in a feed conduit 502 that is passed through the first adsorbent bed 504 and conducting a product stream away from the first adsorbent bed 504 via product conduit 506. A second adsorbent bed 510 is shown performing a cooling step with the cooling stream in a purge conduit 508 that is passed through the second adsorbent bed 510 and conducting a cooling product stream away from the second adsorbent bed 510. A third adsorbent bed 514 is shown performing a heating step or regeneration step with the purge product stream that is passed through a heating unit 512 and then to the third adsorbent bed 514 and conducting a purge product stream away from the third adsorbent bed 514 via the product conduit 516. A fourth adsorbent bed 518 is shown in a stand-by with no streams being passed through the fourth adsorbent bed 518.


In this configuration, the purge stream (which may be at or near ambient temperatures) is first passed in a co-current direction to the feed direction of the feed stream to cool a recently regenerated second adsorbent bed 510. The cooling step lessens the temperature of the second adsorbent bed 510, while recovering some of the heat in the second adsorbent bed 510. The resulting gas stream is then heated and introduced to a spent third adsorbent bed 514 to regenerate the third adsorbent bed 514. This configuration has the additional advantage of recovering some of the heat from the regeneration process. In certain configurations, the purge gas exiting the adsorbent bed after the cooling step is largely devoid of contaminant as the purge gas is flowing along the feed direction. In other configurations, the purge gas stream may be in fluid communication (e.g., tied to) with an LNG dehydration process. In such configurations, the source of the purge gas stream may be adjusted to provide enhancements. Additionally, the cooling process may be continuous (e.g., at least one adsorbent bed that is being cooled at any instant of time).



FIG. 6 is an exemplary diagram 600 of product gas temperature from a swing adsorption process. In this diagram 600, the temperature response 606 is shown along a temperature axis 604 in Celsius (C) and a cycle time axis 602 in seconds (s). An example for the second configuration, as shown in FIG. 5, the temperature swing of the product end is dampened from 175° C. to 29° C. (e.g., no cooling step) from 39° C. to 29° C. The additional dampening may be achieved by operating multiple adsorbent beds out of sequence on feed. For example, a new adsorbent bed may be introduced on feed, while a different adsorbent bed is already operational and producing product at nearly the feed temperature.


In one or more embodiments, the material may include an adsorbent material supported on a non-adsorbent support. The adsorbent materials may include alumina, microporous zeolites, carbons, cationic zeolites, high silica zeolites, highly siliceous ordered it) mesoporous materials, sol gel materials, aluminum phosphorous and oxygen (ALPO) materials (microporous and mesoporous materials containing predominantly aluminum phosphorous and oxygen), silicon aluminum phosphorous and oxygen (SAPO) materials (microporous and mesoporous materials containing predominantly silicon aluminum phosphorous and oxygen), metal organic framework (MOF) materials (microporous and mesoporous materials comprised of a metal organic framework) and zeolitic imidazolate frameworks (ZIF) materials (microporous and mesoporous materials comprised of zeolitic imidazolate frameworks). Other materials include microporous and mesoporous sorbents functionalized with functional groups. Examples of functional groups include primary, secondary, tertiary amines and other non protogenic basic groups such as amidines, guanidines and biguanides.


In one or more embodiments, the adsorbent bed unit may be utilized to separate contaminants from a feed stream during normal operation mode. The method may include a) passing a gaseous feed stream at a feed pressure through an adsorbent bed unit having an adsorbent contactor to separate one or more contaminants from the gaseous feed stream to form a product stream, wherein the adsorbent contactor has a first portion and a second portion; b) interrupting the flow of the gaseous feed stream; performing a depressurization step, wherein the depressurization step reduces the pressure within the adsorbent bed unit; c) performing an optional heating step, wherein the heating step increases the temperature of the adsorbent bed unit to form a temperature differential between the feed end of the adsorbent bed and the product end of the adsorbent bed; and d) performing a cooling step, wherein the cooling step reduces the temperature within the adsorbent bed unit; e) performing a re-pressurization step, wherein the re-pressurization step increases the pressure within the adsorbent bed unit; and repeating the steps a) to e) for at least one additional cycle.


In one or more embodiments, when using RCTSA or an integrated RCPSA and RCTSA process, the total cycle times are typically less than 600 seconds, preferably less than 400 seconds, preferably less than 300 seconds, preferably less than 250 seconds, preferably less than 180 seconds, more preferably less than 90 seconds, and even more preferably less than 60 seconds. In other embodiment, the rapid cycle configuration may be operated at lower flow rates during startup mode as compared to normal operation mode, which may result in the cycle durations being longer than the cycle durations during normal operation mode. For example, the cycle duration may be extended to 1,000 seconds for some cycles.


In view of the many possible embodiments to which the principles of the disclosed invention may be applied, it should be recognized that the illustrative embodiments are only at preferred examples of the invention and should not be taken as limiting the scope of the invention.

Claims
  • 1. A process for removing contaminants from a gaseous feed stream with a swing adsorption process, the process comprising: a) performing an adsorption step, wherein the adsorption step comprises passing the gaseous feed stream through an adsorbent bed unit to remove one or more contaminants and produce a product stream;b) interrupting a flow of the gaseous feed stream;c) performing a heating step, wherein the heating step comprises passing a heating stream through the adsorbent bed unit to remove the one or more contaminants from the adsorbent bed unit;d) performing a cooling step, wherein the cooling step comprises lessening a temperature of an adsorbent material in the adsorbent bed unit by passing a cooling stream through the adsorbent bed unit;e) repeating the steps a) to d) for at least one additional cycle in the swing adsorption process; andf) wherein the swing adsorption process dampens one or more of temperature, compositional, and pressure pulses associated with transition of different streams through the adsorbent bed unit between steps in the swing adsorption process.
  • 2. The process of claim 1, wherein a duration of the cycles is for a period greater than 1 second and less than 600 seconds.
  • 3. The process of claim 2, wherein the gaseous feed stream is a hydrocarbon containing stream having greater than one volume percent hydrocarbons based on a total volume of the gaseous feed stream.
  • 4. The process of claim 3, wherein the gaseous feed stream comprises hydrocarbons and carbon dioxide (CO2), wherein a CO2 content of the gaseous feed stream is from about 200 parts per million volume to about 2% volume of the gaseous feed stream; and the swing adsorption process lowers the CO2 in the product stream to less than 50 parts per million.
  • 5. The process of claim 3, further comprising passing the product stream to a downstream process selected from a liquefied natural gas (LNG) process that comprises an LNG process unit, and a cryogenic natural gas liquefaction (NGL) process having a NGL process unit.
  • 6. The process of claim 2, wherein the cooling stream is passed from the adsorbent bed unit to a conditioning unit to produce a conditioned stream; and the conditioned stream is passed from the conditioning unit to an additional adsorbent bed unit as the heating stream.
  • 7. The process of claim 6, wherein the heating stream is passed through the adsorbent bed unit in a direction that is counter-current to a direction that the gaseous feed stream is passed through the adsorbent bed unit; and the cooling stream is passed through the adsorbent bed unit in a direction that is counter-current to the direction that the gaseous feed stream is passed through the adsorbent bed unit.
  • 8. The process of claim 6, further comprising splitting a purge stream into the heating stream and the cooling stream, wherein the cooling stream is passed through the adsorbent bed unit in a direction that is co-current to a direction that the gaseous feed stream is passed through the adsorbent bed unit; and the heating stream is passed through the adsorbent bed unit in a direction that is counter-current to the direction that the gaseous feed stream is passed through the adsorbent bed unit.
  • 9. The process of claim 6, further comprising determining whether the product stream is within an acceptable temperature limit, and the acceptable temperature limit is selected from: wherein the product stream temperature is within about 50° F. of the temperature of the gaseous feed stream;wherein the product stream temperature is within about 25° F. of the temperature of the gaseous feed stream; andwherein the product stream temperature is within about 10° F. of the temperature of the gaseous feed stream.
  • 10. The process of claim 6, wherein the swing adsorption process is a rapid cycle temperature swing adsorption process or a combined a rapid cycle temperature swing adsorption/rapid cycle pressure swing adsorption process.
  • 11. The process of claim 1, wherein the swing adsorption process is performed with sufficient thermal capacitance to dampen the temperature pulses in the product stream.
CROSS-REFERENCE TO RELATED APPLICATION

This application is a divisional of U.S. patent application Ser. No. 16/252,975 filed Jan. 21, 2019, which claims the benefit of U.S. Provisional Patent Application 62/621,246 filed Jan. 24, 2018 entitled APPARATUS AND SYSTEM FOR SWING ADSORPTION PROCESSES, the entirety of each of which is incorporated by reference herein.

US Referenced Citations (461)
Number Name Date Kind
1868138 Fisk Jul 1932 A
3103425 Meyer Sep 1963 A
3124152 Payne Mar 1964 A
3142547 Marsh et al. Jul 1964 A
3508758 Strub Apr 1970 A
3594983 Yearout Jul 1971 A
3602247 Bunn et al. Aug 1971 A
3788036 Lee et al. Jan 1974 A
3967464 Cormier et al. Jul 1976 A
4187092 Woolley Feb 1980 A
4261815 Kelland Apr 1981 A
4324565 Benkmann Apr 1982 A
4325565 Winchell Apr 1982 A
4329162 Pitcher May 1982 A
4340398 Doshi et al. Jul 1982 A
4386947 Mizuno et al. Jun 1983 A
4421531 Dalton, Jr. et al. Dec 1983 A
4445441 Tanca May 1984 A
4461630 Cassidy et al. Jul 1984 A
4496376 Hradek Jan 1985 A
4631073 Null et al. Dec 1986 A
4693730 Miller et al. Sep 1987 A
4705627 Miwa et al. Nov 1987 A
4711968 Oswald et al. Dec 1987 A
4737170 Searle Apr 1988 A
4770676 Sircar Sep 1988 A
4783205 Searle Nov 1988 A
4784672 Sircar Nov 1988 A
4790272 Woolenweber Dec 1988 A
4814146 Brand et al. Mar 1989 A
4816039 Krishnamurthy et al. Mar 1989 A
4877429 Hunter Oct 1989 A
4977745 Heichberger Dec 1990 A
5110328 Yokota et al. May 1992 A
5125934 Krishnamurthy et al. Jun 1992 A
5169006 Stelzer Dec 1992 A
5174796 Davis et al. Dec 1992 A
5224350 Mehra Jul 1993 A
5234472 Krishnamurthy et al. Aug 1993 A
5292990 Kantner et al. Mar 1994 A
5306331 Auvil et al. Apr 1994 A
5354346 Kumar Oct 1994 A
5365011 Ramachandran et al. Nov 1994 A
5370728 LaSala et al. Dec 1994 A
5486227 Kumar et al. Jan 1996 A
5547641 Smith et al. Aug 1996 A
5565018 Baksh et al. Oct 1996 A
5672196 Acharya et al. Sep 1997 A
5700310 Bowman et al. Dec 1997 A
5733451 Coellner et al. Mar 1998 A
5735938 Baksh et al. Apr 1998 A
5750026 Gadkaree et al. May 1998 A
5769928 Leavitt Jun 1998 A
5779768 Anand et al. Jul 1998 A
5792239 Reinhold, III et al. Aug 1998 A
5807423 Lemcoff et al. Sep 1998 A
5811616 Holub et al. Sep 1998 A
5827358 Kulish et al. Oct 1998 A
5882380 Sircar Mar 1999 A
5906673 Reinhold, III et al. May 1999 A
5912426 Smolarek et al. Jun 1999 A
5914294 Park et al. Jun 1999 A
5924307 Nenov Jul 1999 A
5935444 Johnson et al. Aug 1999 A
5968234 Midgett, II et al. Oct 1999 A
5976221 Bowman et al. Nov 1999 A
5997617 Czabala et al. Dec 1999 A
6007606 Baksh et al. Dec 1999 A
6011192 Baker et al. Jan 2000 A
6023942 Thomas et al. Feb 2000 A
6053966 Moreau et al. Apr 2000 A
6063161 Keefer et al. May 2000 A
6096115 Kleinberg et al. Aug 2000 A
6099621 Ho Aug 2000 A
6102985 Naheiri et al. Aug 2000 A
6129780 Millet et al. Oct 2000 A
6136222 Friesen et al. Oct 2000 A
6147126 DeGeorge et al. Nov 2000 A
6152991 Ackley Nov 2000 A
6156101 Naheiri Dec 2000 A
6171371 Derive et al. Jan 2001 B1
6176897 Keefer Jan 2001 B1
6179900 Behling et al. Jan 2001 B1
6183538 Naheiri Feb 2001 B1
6194079 Hekal Feb 2001 B1
6210466 Whysall et al. Apr 2001 B1
6231302 Bonardi May 2001 B1
6245127 Kane et al. Jun 2001 B1
6284021 Lu et al. Sep 2001 B1
6311719 Hill et al. Nov 2001 B1
6345954 Al-Himyary et al. Feb 2002 B1
6398853 Keefer et al. Jun 2002 B1
6402813 Monereau et al. Jun 2002 B2
6406523 Connor et al. Jun 2002 B1
6425938 Xu et al. Jul 2002 B1
6432379 Heung Aug 2002 B1
6436171 Wang et al. Aug 2002 B1
6444012 Dolan et al. Sep 2002 B1
6444014 Mullhaupt et al. Sep 2002 B1
6444523 Fan et al. Sep 2002 B1
6444610 Yamamoto Sep 2002 B1
6451095 Keefer et al. Sep 2002 B1
6457485 Hill et al. Oct 2002 B2
6458187 Fritz et al. Oct 2002 B1
6464761 Bugli Oct 2002 B1
6471749 Kawai et al. Oct 2002 B1
6471939 Boix et al. Oct 2002 B1
6488747 Keefer Dec 2002 B1
6497750 Butwell et al. Dec 2002 B2
6500234 Ackley et al. Dec 2002 B1
6500241 Reddy Dec 2002 B2
6500404 Camblor Fernandez et al. Dec 2002 B1
6503299 Baksh et al. Jan 2003 B2
6506351 Jain et al. Jan 2003 B1
6514318 Keefer Feb 2003 B2
6514319 Keefer et al. Feb 2003 B2
6517609 Monereau et al. Feb 2003 B1
6531516 Davis et al. Mar 2003 B2
6533846 Keefer et al. Mar 2003 B1
6565627 Golden et al. May 2003 B1
6565635 Keefer et al. May 2003 B2
6565825 Ohji et al. May 2003 B2
6572678 Wijmans et al. Jun 2003 B1
6579341 Baker et al. Jun 2003 B2
6593541 Herren Jul 2003 B1
6595233 Pulli Jul 2003 B2
6605136 Graham et al. Aug 2003 B1
6607584 Moreau et al. Aug 2003 B2
6630012 Wegeng et al. Oct 2003 B2
6631626 Hahn Oct 2003 B1
6641645 Lee et al. Nov 2003 B1
6651645 Nunez-Suarez Nov 2003 B1
6660064 Golden et al. Dec 2003 B2
6660065 Byrd et al. Dec 2003 B2
6692626 Keefer et al. Feb 2004 B2
6712087 Hill et al. Mar 2004 B2
6742507 Keefer et al. Jun 2004 B2
6746515 Wegeng et al. Jun 2004 B2
6752852 Jacksier et al. Jun 2004 B1
6770120 Neu et al. Aug 2004 B2
6773225 Yuri et al. Aug 2004 B2
6802889 Graham et al. Oct 2004 B2
6814771 Scardino et al. Nov 2004 B2
6835354 Woods et al. Dec 2004 B2
6840985 Keefer Jan 2005 B2
6866950 Connor et al. Mar 2005 B2
6889710 Wagner May 2005 B2
6890376 Arquin et al. May 2005 B2
6893483 Golden et al. May 2005 B2
6902602 Keefer et al. Jun 2005 B2
6916358 Nakamura et al. Jul 2005 B2
6918953 Lomax, Jr. et al. Jul 2005 B2
6921597 Keefer et al. Jul 2005 B2
6974496 Wegeng et al. Dec 2005 B2
7025801 Monereau Apr 2006 B2
7027929 Wang Apr 2006 B2
7029521 Johansson Apr 2006 B2
7074323 Ghijsen Jul 2006 B2
7077891 Jaffe et al. Jul 2006 B2
7087331 Keefer et al. Aug 2006 B2
7094275 Keefer et al. Aug 2006 B2
7097925 Keefer et al. Aug 2006 B2
7112239 Kimbara et al. Sep 2006 B2
7117669 Kaboord et al. Oct 2006 B2
7122073 Notaro et al. Oct 2006 B1
7128775 Celik et al. Oct 2006 B2
7144016 Gozdawa Dec 2006 B2
7160356 Koros et al. Jan 2007 B2
7160367 Babicki et al. Jan 2007 B2
7166149 Dunne et al. Jan 2007 B2
7172645 Pfister et al. Feb 2007 B1
7189280 Alizadeh-Khiavi et al. Mar 2007 B2
7243679 Thelen Jul 2007 B2
7250073 Keefer et al. Jul 2007 B2
7250074 Tonkovich et al. Jul 2007 B2
7255727 Monereau et al. Aug 2007 B2
7258725 Ohmi et al. Aug 2007 B2
7276107 Baksh et al. Oct 2007 B2
7279029 Occhialini et al. Oct 2007 B2
7285350 Keefer et al. Oct 2007 B2
7297279 Johnson et al. Nov 2007 B2
7311763 Neary Dec 2007 B2
RE40006 Keefer et al. Jan 2008 E
7314503 Landrum et al. Jan 2008 B2
7354562 Ying et al. Apr 2008 B2
7387849 Keefer et al. Jun 2008 B2
7390350 Weist, Jr. et al. Jun 2008 B2
7404846 Golden et al. Jul 2008 B2
7438079 Cohen et al. Oct 2008 B2
7449049 Thomas et al. Nov 2008 B2
7456131 Klett et al. Nov 2008 B2
7510601 Whitley et al. Mar 2009 B2
7527670 Ackley et al. May 2009 B2
7553568 Keefer Jun 2009 B2
7578864 Watanabe et al. Aug 2009 B2
7604682 Seaton Oct 2009 B2
7637989 Bong Dec 2009 B2
7641716 Lomax, Jr. et al. Jan 2010 B2
7645324 Rode et al. Jan 2010 B2
7651549 Whitley Jan 2010 B2
7674319 Lomax, Jr. et al. Mar 2010 B2
7674539 Keefer et al. Mar 2010 B2
7687044 Keefer et al. Mar 2010 B2
7713333 Rege et al. May 2010 B2
7717981 LaBuda et al. May 2010 B2
7722700 Sprinkle May 2010 B2
7731782 Kelley et al. Jun 2010 B2
7740687 Reinhold, III Jun 2010 B2
7744676 Leitmayr et al. Jun 2010 B2
7744677 Barclay et al. Jun 2010 B2
7758051 Roberts-Haritonov et al. Jul 2010 B2
7758988 Keefer et al. Jul 2010 B2
7763098 Alizadeh-Khiavi et al. Jul 2010 B2
7763099 Verma et al. Jul 2010 B2
7792983 Mishra et al. Sep 2010 B2
7793675 Cohen et al. Sep 2010 B2
7806965 Stinson Oct 2010 B2
7819948 Wagner Oct 2010 B2
7828877 Sawada et al. Nov 2010 B2
7828880 Moriya et al. Nov 2010 B2
7854793 Rarig et al. Dec 2010 B2
7858169 Yamashita Dec 2010 B2
7862645 Whitley et al. Jan 2011 B2
7867320 Baksh et al. Jan 2011 B2
7902114 Bowie et al. Mar 2011 B2
7938886 Hershkowitz et al. May 2011 B2
7947118 Rarig et al. May 2011 B2
7947120 Deckman et al. May 2011 B2
7959720 Deckman et al. Jun 2011 B2
8016918 LaBuda et al. Sep 2011 B2
8034164 Lomax, Jr. et al. Oct 2011 B2
8071063 Reyes et al. Dec 2011 B2
8128734 Song Mar 2012 B2
8142745 Reyes et al. Mar 2012 B2
8142746 Reyes et al. Mar 2012 B2
8192709 Reyes et al. Jun 2012 B2
8210772 Gillecriosd Jul 2012 B2
8227121 Adams et al. Jul 2012 B2
8262773 Northrop et al. Sep 2012 B2
8262783 Stoner et al. Sep 2012 B2
8268043 Celik et al. Sep 2012 B2
8268044 Wright et al. Sep 2012 B2
8272401 McLean Sep 2012 B2
8287629 Fujita et al. Oct 2012 B2
8319090 Kitamura Nov 2012 B2
8337594 Corma Canos et al. Dec 2012 B2
8361200 Sayari et al. Jan 2013 B2
8361205 Desai et al. Jan 2013 B2
8377173 Chuang Feb 2013 B2
8444750 Deckman et al. May 2013 B2
8449649 Greenough May 2013 B2
8470395 Khiavi et al. Jun 2013 B2
8480795 Siskin et al. Jul 2013 B2
8512569 Eaton et al. Aug 2013 B2
8518356 Schaffer et al. Aug 2013 B2
8529662 Kelley et al. Sep 2013 B2
8529663 Reyes et al. Sep 2013 B2
8529664 Deckman et al. Sep 2013 B2
8529665 Manning et al. Sep 2013 B2
8535414 Johnson et al. Sep 2013 B2
8545602 Chance et al. Oct 2013 B2
8551444 Agnihotri et al. Oct 2013 B2
8573124 Havran et al. Nov 2013 B2
8591627 Jain Nov 2013 B2
8591634 Winchester et al. Nov 2013 B2
8616233 McLean et al. Dec 2013 B2
8657922 Yamawaki et al. Feb 2014 B2
8673059 Leta et al. Mar 2014 B2
8680344 Weston et al. Mar 2014 B2
8715617 Genkin et al. May 2014 B2
8752390 Wright et al. Jun 2014 B2
8753428 Lomax, Jr. et al. Jun 2014 B2
8778051 Weist, Jr. et al. Jul 2014 B2
8784533 Leta et al. Jul 2014 B2
8784534 Kamakoti et al. Jul 2014 B2
8784535 Ravikovitch et al. Jul 2014 B2
8790618 Adams et al. Jul 2014 B2
8795411 Hufton et al. Aug 2014 B2
8808425 Genkin et al. Aug 2014 B2
8808426 Sundaram Aug 2014 B2
8814985 Gerds et al. Aug 2014 B2
8852322 Gupta et al. Oct 2014 B2
8858683 Deckman Oct 2014 B2
8875483 Wettstein Nov 2014 B2
8906138 Rasmussen et al. Dec 2014 B2
8921637 Sundaram et al. Dec 2014 B2
8936669 Doong et al. Jan 2015 B2
8939014 Kamakoti et al. Jan 2015 B2
9005561 Leta Apr 2015 B2
9017457 Tammera Apr 2015 B2
9028595 Sundaram et al. May 2015 B2
9034078 Wanni et al. May 2015 B2
9034079 Deckman et al. May 2015 B2
9050553 Alizadeh-Khiavi et al. Jun 2015 B2
9067168 Frederick et al. Jun 2015 B2
9067169 Patel Jun 2015 B2
9095809 Deckman et al. Aug 2015 B2
9108145 Kalbassi et al. Aug 2015 B2
9120049 Sundaram et al. Sep 2015 B2
9126138 Deckman et al. Sep 2015 B2
9162175 Sundaram Oct 2015 B2
9168483 Ravikovitch et al. Oct 2015 B2
9168485 Deckman et al. Oct 2015 B2
9272264 Coupland Mar 2016 B2
9278338 Coupland Mar 2016 B2
9358493 Tammera et al. Jun 2016 B2
9573116 Johnson et al. Feb 2017 B2
9597655 Beeckman Mar 2017 B2
9737846 Carstensen et al. Aug 2017 B2
9744521 Brody et al. Aug 2017 B2
10040022 Fowler et al. Aug 2018 B2
10080991 Johnson et al. Sep 2018 B2
10080992 Nagavarapu et al. Sep 2018 B2
10124286 McMahon et al. Nov 2018 B2
20010047824 Hill et al. Dec 2001 A1
20020053547 Schlegel et al. May 2002 A1
20020124885 Hill et al. Sep 2002 A1
20020162452 Butwell et al. Nov 2002 A1
20030075485 Ghijsen Apr 2003 A1
20030129101 Zettel Jul 2003 A1
20030131728 Kanazirev et al. Jul 2003 A1
20030145726 Gueret et al. Aug 2003 A1
20030170527 Finn et al. Sep 2003 A1
20030188635 Lomax, Jr. et al. Oct 2003 A1
20030202918 Ashida et al. Oct 2003 A1
20030205130 Neu et al. Nov 2003 A1
20030223856 Yuri et al. Dec 2003 A1
20040099142 Arquin et al. May 2004 A1
20040118277 Kim Jun 2004 A1
20040118747 Cutler et al. Jun 2004 A1
20040197596 Connor et al. Oct 2004 A1
20040232622 Gozdawa Nov 2004 A1
20050014511 Spain et al. Jan 2005 A1
20050045041 Hechinger et al. Mar 2005 A1
20050109419 Ohmi et al. May 2005 A1
20050114032 Wang May 2005 A1
20050129952 Sawada et al. Jun 2005 A1
20050145111 Keefer et al. Jul 2005 A1
20050150378 Dunne et al. Jul 2005 A1
20050229782 Monereau et al. Oct 2005 A1
20050252378 Celik et al. Nov 2005 A1
20060017940 Takayama Jan 2006 A1
20060048648 Gibbs et al. Mar 2006 A1
20060049102 Miller et al. Mar 2006 A1
20060076270 Poshusta et al. Apr 2006 A1
20060099096 Shaffer et al. May 2006 A1
20060105158 Fritz et al. May 2006 A1
20060116430 Wentink et al. Jun 2006 A1
20060116460 Georget et al. Jun 2006 A1
20060162556 Ackley et al. Jul 2006 A1
20060165574 Sayari Jul 2006 A1
20060169142 Rode et al. Aug 2006 A1
20060236862 Golden et al. Oct 2006 A1
20070084241 Kretchmer et al. Apr 2007 A1
20070084344 Moriya et al. Apr 2007 A1
20070222160 Roberts-Haritonov Sep 2007 A1
20070253872 Keefer et al. Nov 2007 A1
20070261550 Ota Nov 2007 A1
20070261557 Gadkaree Nov 2007 A1
20070283807 Whitley Dec 2007 A1
20080051279 Klett et al. Feb 2008 A1
20080072822 White Mar 2008 A1
20080128655 Garg et al. Jun 2008 A1
20080202336 Hofer et al. Aug 2008 A1
20080282883 Rarig et al. Nov 2008 A1
20080282884 Kelley et al. Nov 2008 A1
20080282885 Deckman et al. Nov 2008 A1
20080282886 Reyes et al. Nov 2008 A1
20080282887 Chance et al. Nov 2008 A1
20080282892 Deckman et al. Nov 2008 A1
20080289497 Barclay et al. Nov 2008 A1
20080307966 Stinson Dec 2008 A1
20080314550 Greco Dec 2008 A1
20090004073 Gleize et al. Jan 2009 A1
20090014902 Koivunen et al. Jan 2009 A1
20090025553 Keefer et al. Jan 2009 A1
20090025555 Lively et al. Jan 2009 A1
20090037550 Mishra et al. Feb 2009 A1
20090071333 LaBuda et al. Mar 2009 A1
20090079870 Matsui Mar 2009 A1
20090107332 Wagner Apr 2009 A1
20090151559 Verma et al. Jun 2009 A1
20090162268 Hufton et al. Jun 2009 A1
20090180423 Kroener Jul 2009 A1
20090241771 Manning et al. Oct 2009 A1
20090284013 Anand et al. Nov 2009 A1
20090294366 Wright et al. Dec 2009 A1
20090308248 Siskin et al. Dec 2009 A1
20090314159 Haggerty Dec 2009 A1
20100059701 McLean Mar 2010 A1
20100077920 Baksh et al. Apr 2010 A1
20100089241 Stoner et al. Apr 2010 A1
20100186445 Minta et al. Jul 2010 A1
20100212493 Rasmussen et al. Aug 2010 A1
20100251887 Jain Oct 2010 A1
20100252497 Ellison et al. Oct 2010 A1
20100263534 Chuang Oct 2010 A1
20100282593 Speirs et al. Nov 2010 A1
20100288704 Amsden et al. Nov 2010 A1
20110011803 Koros Jan 2011 A1
20110020202 Gadkaree et al. Jan 2011 A1
20110031103 Deckman et al. Feb 2011 A1
20110067440 Van Aken Mar 2011 A1
20110067770 Pederson et al. Mar 2011 A1
20110123878 Jangbarwala May 2011 A1
20110146494 Desai et al. Jun 2011 A1
20110217218 Gupta et al. Sep 2011 A1
20110277620 Havran et al. Nov 2011 A1
20110291051 Hershkowitz et al. Dec 2011 A1
20110296871 Van Soest-Vercammen et al. Dec 2011 A1
20110308524 Brey et al. Dec 2011 A1
20120024150 Moniot Feb 2012 A1
20120024152 Yamawaki et al. Feb 2012 A1
20120031144 Northrop et al. Feb 2012 A1
20120067216 Corma Canos et al. Mar 2012 A1
20120152115 Gerds et al. Jun 2012 A1
20120222551 Deckman Sep 2012 A1
20120222552 Ravikovitch et al. Sep 2012 A1
20120222553 Kamakoti et al. Sep 2012 A1
20120222554 Leta et al. Sep 2012 A1
20120222555 Gupta et al. Sep 2012 A1
20120255377 Kamakoti et al. Oct 2012 A1
20120272823 Halder et al. Nov 2012 A1
20120308456 Leta et al. Dec 2012 A1
20120312163 Leta Dec 2012 A1
20130061755 Frederick et al. Mar 2013 A1
20130095996 Buelow et al. Apr 2013 A1
20130225898 Sundaram et al. Aug 2013 A1
20140013955 Tammera et al. Jan 2014 A1
20140060326 Sundaram et al. Mar 2014 A1
20140157984 Deckman et al. Jun 2014 A1
20140157986 Ravikovitch et al. Jun 2014 A1
20140208797 Kelley et al. Jul 2014 A1
20140216254 Tammera et al. Aug 2014 A1
20140326136 Doong Nov 2014 A1
20150013377 Oelfke Jan 2015 A1
20150068397 Boulet et al. Mar 2015 A1
20150101483 Perry et al. Apr 2015 A1
20150196870 Albright et al. Jul 2015 A1
20150328578 Deckman et al. Nov 2015 A1
20160023155 Ramkumar et al. Jan 2016 A1
20160129433 Tannera et al. May 2016 A1
20160166972 Owens et al. Jun 2016 A1
20160236135 Tammera et al. Aug 2016 A1
20160332105 Tammera et al. Nov 2016 A1
20160332106 Tammera Nov 2016 A1
20170056810 Johnson Mar 2017 A1
20170056814 Marshall et al. Mar 2017 A1
20170113173 Fowler et al. Apr 2017 A1
20170113175 Fowler et al. Apr 2017 A1
20170136405 Ravikovitch et al. May 2017 A1
20170266604 Tammera et al. Sep 2017 A1
20170282114 Owens et al. Oct 2017 A1
20170341011 Nagavarapu et al. Nov 2017 A1
20170341012 Nagavarapu et al. Nov 2017 A1
20180001301 Brody et al. Jan 2018 A1
20180056229 Denton et al. Mar 2018 A1
20180056235 Wang et al. Mar 2018 A1
20180169565 Brody et al. Jun 2018 A1
20180169617 Brody et al. Jun 2018 A1
20180339263 Dehaas et al. Nov 2018 A1
Foreign Referenced Citations (27)
Number Date Country
0257493 Feb 1988 EP
0426937 May 1991 EP
0904827 Mar 1999 EP
1674555 Jun 2006 EP
2823872 Jan 2015 EP
2854819 May 2003 FR
2924951 Jun 2009 FR
58-114715 Jul 1983 JP
59-232174 Dec 1984 JP
60-189318 Dec 1985 JP
2002-253818 Oct 1990 JP
04-180978 Jun 1992 JP
06006736 Jun 1992 JP
3477280 Aug 1995 JP
2011-169640 Jun 1999 JP
2011-280921 Oct 1999 JP
2000-024445 Aug 2001 JP
2002-348651 Dec 2002 JP
2006-016470 Jan 2006 JP
2006-036849 Feb 2006 JP
2008-272534 Nov 2008 JP
101349424 Jan 2014 KR
WO2002024309 Mar 2002 WO
WO2002073728 Sep 2002 WO
WO2005090793 Sep 2005 WO
WO2010024643 Mar 2010 WO
WO2011139894 Nov 2011 WO
Non-Patent Literature Citations (58)
Entry
Rezaei, F. et al. (2014) “Modeling of Rapid Temperature Swing Adsorption Using Hollow Fiber Sorbents”, Chem. Engineering Science, v. 113, pp. 62-76.
Dubbeldam, D., et al., (2013) “On the inner workings of Monte Carlo codes” Molecular Simulation, vol. 39, Nos. 14-15, pp. 1253-1292.
Earl, D. J. et al., (2005) “Parallel tempering: Theory, applications, and new perspectives,” Phys Chem Chem Phys, vol. 7, pp. 3910-3916.
ExxonMobil Research and Engineering and QuestAir (2008) “A New Commercialized Process for Lower Cost H2 Recovery—Rapid Cycle Pressure Swing Adsorption (RCPSA),” Brochure, 4 pgs.
Fang, H. et al., (2013) “First principles derived, transferable force fields for CO2 adsorption in Na-exchanged cationic zeolites,” Phys Chem Chem Phys, vol. 15, pp. 12882-12894.
Fang, H., et al., (2012) “Prediction of CO2 Adsorption Properties in Zeolites Using Force Fields Derived from Periodic Dispersion-Corrected DFT Calculations, ” J Phys Chem C, 10692, 116, ACS Publications.
Farooq, S. et al. (1990) “Continuous Countercurrent Flow Model for a Bulk PSA Separation Process,” AIChE J., v36 (2) p. 310-314.
FlowServe (2005) “Exceeding Expectations, US Navy Cuts Maintenance Costs With Flowserve GX-200 Non-Contacting Seal Retrofits,” Face-to-Face, v17.1, 8 pgs.
Foster, M.D., et al. “A geometric solution to the largest-free-sphere problem in zeolite frameworks”, Microporous and Mesoporous Materials, vol. 90, pp. 32-38.
Frenkel, D. et al., (2002) “Understanding Molecular Simulation: From Algorithms to Applications”, 2nd ed., Academic Press, pp. 292-301.
Garcia, E. J., et al. (2014) “Tuning the Adsorption Properties of Zeolites as Adsorbents for CO2 Separation: Best Compromise between the Working Capacity and Selectivity”, Ind. Eng. Chem. Res., vol. 53, pp. 9860-9874.
GE Oil & Gas (2007) “Dry Gas Seal Retrofit,” Florene, Italy, www.ge.com/oilandgas, 4 pgs.
Harris, J. G. et al., (1995) “Carbon Dioxide's Liquid—Vapor Coexistence Curve and Critical Properties as Predicted by a Simple Molecular Model”, J Phys Chem, vol. 99, pp. 12021-12024.
Hill, J. R. et al., (1995) “Molecular Mechanics Potential for Silica and Zeolite Catalysts Based on ab Initio Calculations. 2. Aluminosilicates”, J Phys Chem, vol. 99, pp. 9536-9550.
Hopper, B. et al. (2008) “World's First 10,000 psi Sour Gas Injection Compressor,” Proceedings of the 37th Turbomachinery Symposium, pp. 73-95.
Jain, S., et al. (2003) “Heuristic design of pressure swing adsorption: a preliminary study”, Separation and Purification Technology, vol. 33, pp. 25-43.
Kim J. et al. (2012) “Predicting Large CO2 Adsorption in Aluminosilicate Zeolites for Postcombustion Carbon Dioxide Capture”, J. Am. Chem, Soc., vol. 134, pp. 18940-18940.
Kärger, J., et al.(2012) “Diffusion in Nanoporous Materials” , Whiley-VCH publisher, vol. 1, Chapter 16, pp. 483-501.
Kikkinides, E. S. et al. (1995) “Natural Gas Desulfurization by Adsorption: Feasibility and Multiplicity of Cyclic Steady States,” Ind. Eng. Chem. Res. V. 34, pp. 255-262.
Lin, L., et al. (2012) “In silico screening of carbon-capture materials”, Nature Materials, vol. 1, pp. 633-641.
Liu, Q. et al., (2010) “NaKA sorbents with high CO2-over-N2 selectivity and high capacity to adsorb CO2,” Chem Commun, , vol. 46, pp. 4502-4504.
Lowenstein, W., (1954) “The Distribution of Aluminum in the Tetra-Hedra of Silicates and Aluminates” Am Mineral, 92-96.
Neimark, A. V. et al., (1997) “Calibration of Pore vol. in Adsorption Experiments and Theoretical Models”, Langmuir, vol. 13, pp. 5148-5160.
Palomino, M., et al. (2009) “New Insights on CO2-Methane Seapration Using LTA Zeolites with Different Si/Al Ratios and a First Comparison with MOFs”, Langmar, vol. 26(3), pp. 1910-1917.
Patcas, F.C. et al.(2007) “CO Oxidation Over Structured Carriers: A Comparison of Ceramic Forms, Honeycombs and Beads”, Chem Engineering Science, v. 62, pp. 3984-3990.
Peng, D. Y., et al., (1976) “A New Two-Constant Equation of State”, Ind Eng Chem Fundam, vol. 15, pp. 59-64.
Pham, T. D. et al., (2013) “Carbon Dioxide and Nitrogen Adsorption on Cation-Exchanged SSZ-13 Zeolites”, Langmuir, vol. 29, pp. 832-839.
Pophale, R., et al., (2011) “A database of new zeolite-like materials”, Phys Chem Chem Phys, vol. 13(27), pp. 12407-12412.
Potoff, J. J. et al., (2001) “Vapor-Liquid Equilibria of Mixtures Containing Alkanes, Carbon Dioxide, and Nitrogen”, AIChE J, vol. 47(7), pp. 1676-1682.
Rameshni, Mahin “Strategies for Sour Gas Field Developments,” Worley Parsons-Brochure, 20 pp.
Reyes, S. C. et al. (1997) “Frequency Modulation Methods for Diffusion and Adsorption Measurements in Porous Solids,” J. Phys. Chem. B. v101, pp. 614-622.
Rezaei, F. et al. (2009) “Optimum Structured Adsorbents for Gas Separation Process”, Chem. Engineering Science, v. 64, pp. 5182-5191.
Richardson, J.T. et al. (2000) “Properties of Ceramic Foam Catalyst Supports: Pressure Dop”, Applied Catalysis A: General v. 204, pp. 19-32.
Robinson, D. B., et al., (1985) “The development of the Peng—Robinson Equation and its Application to Phase Equilibrium in a System Containing Methanol,” Fluid Phase Equilibria, vol. 24, pp. 25-41.
Ruthven, D. M. et al. (1996) “Performance of a Parallel Passage Adsorbent Contactor,” Gas. Sep. Purif., vol. 10, No. 1, pp. 63-73.
Stahley, J. S. (2003) “Design, Operation, and Maintenance Considerations for Improved Dry Gas Seal Reliability in Centrifugal Compressors,” Dresser-Rand, Tech. Paper 134, 15 pages.
Santos, M. S. (2011) “New Cycle configuration to enhance performance of kinetic PSA processes” Chemical Engineering Science 66, pp. 1590-1599.
Snurr, R. Q. et al., (1993) “Prediction of Adsorption of Aromatic Hydrocarbons in Silicalite from Grand Canonical Monte Carlo Simulations with Biased Insertions”, J Phys Chem, vol. 97, pp. 13742-13752.
Stemmet, C.P. et al. (2006) “Solid Foam Packings for Multiphase Reactors: Modelling of Liquid Holdup and Mass Transfer”, Chem. Engineering Research and Design, v. 84(A12), pp. 1134-1141.
Suzuki, M. (1985) “Continuous-Countercurrent-Flow Approximation for Dynamic Steady State Profile of Pressure Swing Adsorption” AIChE Symp. Ser. v81 (242) pp. 67-73.
Talu, O et al., (2001), “Reference potentials for adsorption of helium, argon, methane, and krypton in high-silica zeolites,” Colloids and Surfaces A: Physicochemical and Engineering Aspects, vol. 83-93, pp. 83-93.
Walton, K. S. et al., (2006) “CO2 adsorption in Y and X zeolites modified by alkali metal cation exchange,” Microporous and Mesoporous Mat, vol. 91, pp. 78-84.
Willems, T. F. et al., (2012) “Algorithms and tools for high-throughput geometry-based analysis of crystalline porous materials” Microporous Mesoporous Mat, vol. 149, pp. 134-141.
Zukal, A., et al., (2009) “Isosteric heats of adsorption of carbon dioxide on zeolite MCM-22 modified by alkali metal cations”, Adsorption, vol. 15, pp. 264-270.
U.S. Appl. No. 16/252,975, filed Jan. 21, 2019, Krishna Nagavarapu et al.
U.S. Appl. No. 16/258,266, filed Jan. 25, 2019, Barnes et al.
U.S. Appl. No. 16/263,940, filed Jan. 31, 2019, Johnson.
U.S. Appl. No. 62/783,766, filed Dec. 21, 2019, Fulton et al.
Allen, M. P. et al., (1987) “Computer Simulation of Liquids” Clarendon Press, pp. 156-160.
Asgari, M. et al., (2014) “Designing A Commercial Scale Pressure Swing Adsorber For Hydrogen Purification” Petroleum & Coal, vol. 56(5), pp. 552-561.
Baerlocher, C. et al., (2017) International Zeolite Association's “Database of Zeolite Structures,” available at http://www.iza-structure.org/databases/, downloaded Jun. 15, 2018, 1 page.
Burtch, N.C. et al., (2015) “Molecular-level Insight into Unusual Low Pressure CO2 Affinity in Pillared Metal-Organic Frameworks,” J Am Chem Soc, 135, pp. 7172-7180.
Beauvais, C. et al., (2004) “Distribution of Sodium Cations in Faujasite-Type Zeolite: A Canonical Parallel Tempering Simulation Study,” J Phys Chem B, 108, pp. 399-404.
Cheung, O. et al., (2013) “Adsorption kinetics for CO2 on highly selective zeolites NaKA and nano-NaKA,” Appl Energ, 112, pp. 1326-1336.
Cygan, R. T. et al., (2004) “Molecular Models of Hydroxide, Oxyhydroxide, and Clay Phases and the Development of a General Force Field”, J Phys Chem B, vol. 108, pp. 1255-1266.
Deem, M. W. et al., (2009) “Computational Discovery of New Zeolite-Like Materials”, J Phys Chem C, 113, pp. 21353-21360.
Demiralp, E., et al., (1999) “Morse Stretch Potential Charge Equilibrium Force Field for Ceramics: Application to the Quartz-Stishovite Phase Transition and to Silica Glass”, Physical Review Letters, vol. 82(8), pp. 1708-1711.
Dubbeldam, D. et al. (2016) “RASPA: molecular simulation software for adsorption and diffusion in flexible nanoporous materials” Molecular Simulation, (published online Feb. 26, 2015), vol. 42(2), pp. 81-101.
Related Publications (1)
Number Date Country
20220219109 A1 Jul 2022 US
Provisional Applications (1)
Number Date Country
62621246 Jan 2018 US
Divisions (1)
Number Date Country
Parent 16252975 Jan 2019 US
Child 17707459 US