The present techniques relate to a system associated with a swing adsorption process. In particular, the system includes an adsorbent bed unit whose configuration includes a mid-bed purge system.
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 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 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. The adsorbent material is then typically purged and repressurized. Then, the adsorbent material is ready for another adsorption cycle.
The swing adsorption processes typically involve adsorption units, which include adsorbent bed units. 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. Orchestrating these adsorbent bed units involves coordinating the cycles for each of the adsorbent bed unit 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.
Unfortunately, conventional swing adsorption processes have certain limitations that are inefficient or do not operate properly for purging the contaminants from the adsorbent beds. That is, the conventional adsorbent bed units provide gas streams from one end or the other end of the adsorbent bed. The purging in conventional systems is time consuming and can be inefficient. For engineered packing, the structure of the bed further complicates the purging of fluids from within the engineered packing if the adsorbent bed is formed into a specific configuration.
Accordingly, there remains a need in the industry for apparatus, methods, and systems that provide an enhanced adsorbent bed unit. The present techniques provide a method and apparatus that overcome one or more of the deficiencies discussed above. In particular, the present techniques provide an adsorbent bed unit that includes a mid-bed purge system that enhances the operations of the swing adsorption processes to provide gas from a location other than the end of the adsorbent bed.
In one or more embodiments, the present techniques include an adsorbent bed unit for a cyclical swing process. The adsorbent bed unit includes: a housing having an interior region; one or more contactors disposed in the interior region, each of the one or more contactors having a first portion and a second portion, wherein the first portion is disposed upstream of the second portion, wherein the first portion comprises a first adsorbent material and the second portion comprises a second adsorbent material, and wherein each of the one or more contactors have fluid flow passages through the first adsorbent material and the second adsorbent material; and each of the one or more contactors have at least one gas purge inlet conduit disposed within the first portion and configured to provide a purge flow passage to a mid-purge distribution zone between the first portion and the second portion, wherein the purge flow passage within the at least one gas purge inlet conduit is fluidly separated and independent of the fluid flow passages through the first adsorbent material. The adsorbent bed unit may also include a plenum closure component disposed upstream of the first portion and having a distribution zone, wherein the plenum closure component is configured to: provide fluid communication between the distribution zone and the mid-purge distribution zone via the at least one gas purge inlet conduit; provide fluid communication between a primary fluid zone formed between the first portion and the plenum closure component and a location external to the housing; and isolate direct fluid communication between the distribution zone and the primary fluid zone. Also, the plenum closure component comprises one or more outlet conduits disposed adjacent to the first portion in the primary fluid zone and configured to provide fluid communication between the primary fluid zone and the external location. The mid-purge distribution zone may be positioned at a location that is between 10% and 60% of the length of the adsorbent bed, or at a location that is between 20% and 40% of the length of the adsorbent bed.
Further, in one or more embodiments, a method of manufacturing a contactor is described. The method comprises: fabricating a first portion of a contactor, wherein the first portion is configured to provide first fluid flow passages through a first adsorbent material, wherein the first portion has a gas purge inlet conduit that is configured to provide a purge flow passage through the first portion and the purge flow passage is fluidly separated and independent of the fluid flow passages through the first portion; fabricating a second portion of the contactor comprising a second adsorbent material, wherein the second portion is configured to provide second fluid flow passages through the second adsorbent material; and securing the first portion to the second portion, wherein the gas purge inlet conduit is configured to provide a purge flow passages to a mid-purge distribution zone between the first portion and the second portion, wherein the purge flow passage is fluidly separated and independent of the first fluid flow passages.
In yet other embodiments, a method of manufacturing an adsorbent bed unit is described. The method comprises: fabricating a plurality of contactors, wherein each of the plurality of contactors comprises: a first portion configured to provide first fluid flow passages through a first adsorbent material, wherein the first portion has a gas purge inlet conduit configured to provide a purge flow passage through the first portion and the purge flow passage is fluidly separated and independent of the first fluid flow passages through the first portion; a second portion comprising a second adsorbent material, wherein the second portion is configured to provide second fluid flow passages through the second adsorbent material; wherein the first portion is secured to the second portion; and wherein the gas purge inlet conduit is configured to provide a purge flow passage to a mid-purge distribution zone between the first portion and the second portion, wherein the purge flow passage is fluidly separated and independent of the fluid flow passages; securing two or more plurality of contactors to each other to forma an assembly of contactors; constructing an adsorbent bed unit housing, wherein the an adsorbent bed unit housing has an interior region; and disposing the assemble of contactors into an adsorbent bed unit housing.
A cyclical swing adsorption process for removing contaminants from gas feed streams comprising the steps of: 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; interrupting the flow of the gaseous feed stream; performing a depressurization step, wherein the depressurization step reduces the pressure within the adsorbent bed unit; performing a purge step, wherein the purge step reduces the pressure within the adsorbent bed unit and wherein the purge step involves passing a purge stream to a mid-purge distribution zone between first portion and the second portion; 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. The method may include: passing the purge stream through a distribution zone in a plenum closure component disposed upstream of the first portion prior to passing the purge stream to the mid-purge distribution zone via a at least one gas purge inlet conduit and/or passing the product stream through a primary fluid zone in a plenum closure component disposed upstream of the first portion, wherein the product stream is isolate direct fluid communication between the distribution zone and the primary fluid zone.
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.
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.
The present techniques relate to an adsorbent bed unit having a mid-bed purge system. The mid-bed purge system may include a compact multi-purpose distribution chamber (e.g., the interior of a plenum closure component) configured to transfer a volume of stored fluid through a feed conduit. The distribution chamber also includes an integrated conduit for transferring a separate stream through a portion of the adsorbent bed.
In certain embodiments, the adsorbent bed unit may include different components that are utilized to enhance operations. For example, the adsorbent bed unit may include a gas inlet conduit (e.g., fluid inlet), which is fabricated as an integral component of the mid-bed purge system. Further, a distribution chamber and associated conduits can be fabricated in a sequence that provides a compact configuration with minimal moving components. This configuration may lessen internal hardware utilized and lessen complications in fabrication and reliability by utilizing such components in this configuration.
The configuration of the mid-bed purge system balances the efficiency of the mid-system purge with the internal dead space volume. That is, the mid-system purge system is configured to increase efficiency of the purge step, while minimizing any changes to the internal dead space volume of the unit, if any. Accordingly, the mid-bed purge system may be configured to provide a separate purge gas stream into the absorbent bed at a location, such as a mid-purge distribution zone. As a result, the present techniques provide a mid-bed purge configuration that introduces a separate fluid stream into the absorbent bed at a location referred to as the mid-purge distribution zone, which is different from the ends of the absorbent bed. The mid-purge distribution zone may be positioned at a location along the length of the contactor or adsorbent bed between a first end and a second end as indicated from the primary fluid flow through the contactor or adsorbent bed (e.g. along the path of the feed fluid or other primary fluid being subjected to the adsorption process). The location of mid-purge distribution zone may be determined based on the inlet gas stream, the purge stream, the adsorbent material, contaminants being removed from the respective adsorbent material via the purge step or a combination thereof.
As an example, an adsorbent bed may have fluids (e.g., feed stream) that flow from a first end to a second end along a length of the adsorbent bed. The mid-purge distribution zone may be disposed between a first portion of the adsorbent bed and a second portion of the adsorbent bed. In certain embodiments, the mid-purge distribution zone may be positioned at a location that is substantially at the center of the adsorbent bed, between the first end and the second end. In other configurations, the mid-purge distribution zone may be positioned at a location that is between 10% and 60% of the length of the adsorbent bed measured from the first end, is between 20% and 40% of the length of the adsorbent bed measured from the first end, or is between 25% and 35% of the length of the adsorbent bed measured from the first end. The length of the adsorbent bed may be between 12 inches and 120 inches (0.3048 meters (m) and 3.048 m); between 18 inches and 60 inches (0.4572 m and 1.524 m); and between 24 inches and 48 inches (0.6096 m and 1.2192 m).
Alternatively, in other embodiments, the mid-purge distribution zone may include multiple zones that are distributed at various locations along the length of the adsorbent bed. For example, two mid-purge distribution zones may be utilized with a first mid-purge distribution zone being disposed between a first portion of the adsorbent bed and a second portion of the adsorbent bed and a second mid-purge distribution zone being disposed between a third portion of the adsorbent bed and the second portion of the adsorbent bed. In certain embodiments, the mid-purge distribution zone may be positioned at a location that is substantially equally spaced from the nearest respective ends of the adsorbent bed and the other mid-purge distribution zone. In other configurations, the first mid-purge distribution zone may be positioned at a location that is between 10% and 40% of the length of the adsorbent bed measured from the first end, while the second mid-purge distribution zone may be positioned at a location that is between 60% and 90% of the length of the adsorbent bed measured from the first end; or a first mid-purge distribution zone may be positioned at a location that is between 20% and 35% of the length of the adsorbent bed measured from the first end, while the second mid-purge distribution zone may be positioned at a location that is between 65% and 80% of the length of the adsorbent bed measured from the first end. As may be appreciated, other configurations may include three mid-purge distribution zones, four mid-purge distribution zones or other numbers of mid-purge distribution zones.
The mid-purge distribution zone may divide the adsorbent bed into a different portions based on the number of mid-purge distribution zones. As may be appreciated, the different portions may include the same type of adsorbent material or different portions may include different types of adsorbent material. That is, one configuration may include one adsorbent material for each of the different portions of the adsorbent bed, while another configuration may include a first adsorbent material and a second portion may include a second adsorbent material. If different materials are utilized, each may be selected to remove certain contaminates or to further enhance the purge step.
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 invention can 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, such as pressure/temperature swing adsorption. Exemplary kinetic swing adsorption processes are described in U.S. Pat. Nos. 7,959,720, 8,545,602, 8,529,663, 8,444,750, 8,529,662 and U.S. Patent Publication No. 2014/0013955, which are each herein incorporated by reference in their entirety.
The present techniques provide various enhancements to swing adsorption systems. For example, the enhancements may include uniformly distributed gas streams at select contactor or adsorbent bed locations. Also, the mid-system purge may be utilized to enhance the efficiency of the purge step and to lessen the period of time involved with the purge step. Further, the mid-bed purge system may lessen internal hardware and lessen complications in fabrication and reliability. The present techniques may be further understood with reference to the
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. 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.
As an example, which is discussed further below in
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.
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 shown) 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 (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. 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) is 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.
To provide certain enhancements, the adsorbent bed unit may include a mid-bed purge system. The mid-bed purge system may include one or more plenum closure components, such as plenum closure components 262 and 264, gas purge inlets or conduits (not shown) and one or more gas purge passages (not shown). The plenum closure components may be divided into different regions and/or the gas purge inlets or conduits may be provided to different locations in the adsorbent bed 210. Exemplary components of the adsorbent bed unit are shown in
In this diagram 340, the fluid flow through the contactor 322 and the plenum closure component 342 are shown by various arrows. For example, the passage through the plenum closure component 342 via the gas outlet conduit 360 may be used to as a passage for fluids passing through the adsorbent material or bed of the contactor 322, as indicated by arrows 352 and 353. The passage within the plenum closure component 342 is the passage for fluids into the gas purge inlet conduit 324 and ultimately into the adsorbent material of the contactor 322, as indicated by arrows 354 and 355. The flow passages (e.g., fluid flow passages) along arrows 352 and 353 are fluidly separated and independent of the flow passages (e.g., purge flow passage) along arrow 355 for the length of the gas purge inlet conduit 324, but are shared within the adsorbent material of the contactor 322, as shown by arrow 354. Further, the flow passages along arrows 352, 353, 354 and 355 are substantially parallel with the exception of portion of the flow through the gas purge passage 356.
The mid-bed purge system includes the plenum closure component 342, gas purge inlet conduit 324 and gas purge passage 356. The gas purge inlet conduit 324 may be configured to provide a passage or channel through the adsorbent material to a certain depth 358 within the contactor 322. The depth 358 is based on the location of the mid-purge distribution zone, which may be positioned at a location that is between 10% and 60% of the length of the contactor 322 measured from the first end (with the length being the depth 358 plus the portion of the contactor 322 to the second end which is not shown in this figure). Other embodiments may include depths between 20% and 40% of the length of the contactor 322 measured from the first end, or is between 25% and 35% of the length of the contactor 322 measured from the first end. As an example, the depth 358 may be 8 inches (0.2032 m).
Also, the gas purge passage 356 may be configured to distribute the purge fluid in a uniform manner into the adsorbent material of the contactor 322. The gas purge passage 356 may be a passage having a height 359. The height 359 may be based on the purge fluid being provided to the mid-purge distribution zone, the cross section dimensions of the contactor and any combination thereof. Accordingly, the height 359 may be between 0.10 inches and 1.0 inches (0.00254 m and 0.0254 m), between 0.15 inches and 0.75 inches (0.00381 m and 0.01905 m) and between 0.20 inches and 0.45 inches (0.00508 m and 0.01143 m). As a specific example, the gas purge passage 356 may be a passage having a height 359 of 0.25 inches (0.00635 m).
Further, the plenum closure component 342 may be configured to distribute the purge fluid in a uniform manner into the contactor 322 via the distribution zone of the plenum closure component 342 that has a depth 357. The depth 357 may be based on the purge fluid being provided to the mid-purge distribution zone, the volume of purge fluid to be utilized in the purge step, the cross section dimensions of the contactor and any combination thereof. Accordingly, the depth 357 may be between 0.5 inches and 10 inches (0.0127 m and 0.254 m), between 1.0 inches and 7.5 inches (0.0254 m and 0.1905 m) and between 1.5 inches and 5 inches (0.0381 m and 0.127 m). As an example, the depth 357 may be a passage having a length of 2.75 inches (0.06985 m).
Along with the distribution zone, the plenum closure component 342 is configured to manage the flow of fluids from the end of the contactor 322 via the primary fluid zone. This primary fluid zone 351 is formed between the end of the contactor 322 and the plenum bottom plate 344 of the plenum closure component 342. The number and configuration of outlet conduits may be adjusted to manage the flow of the inlet stream into the primary fluid zone or from the primary fluid zone to a location external to the adsorbent bed unit. The specific configuration of the outlet conduits and the specific depth of the primary fluid zone may be based on the primary fluids (e.g., feed streams, product streams, waste streams and purge streams) being provided to and from the contactor, the uniformity pattern of the fluids, the volume of primary fluid zone, the cross section dimensions of the contactor and any combination thereof. Accordingly, the depth of the primary fluid zone may be between 0.1 inches and 5 inches (0.00254 m and 0.127 m), between 0.2 inches and 4 inches (0.00508 m and 0.1016 m) and/or between 0.4 inches and 3 inches (0.00381 m and 0.01905 m). As an example, the depth of the primary fluid zone may be 0.25 inches (0.00635 m).
Beneficially, the configuration provides various enhancements. For example, the plenum closure component provides flow management, while minimizing the dead volume. Also, the configuration can be fabricated in a manner that provides a compact configuration with minimal or no moving components. That is, this configuration distributes the flow and may lessen hardware spacing constrains. Further, the configuration lessens the complications by providing components that are easy to fabricate and the plenum closure component lessens spacing issues for operation and maintenance of the unit.
As may be appreciated, this fabrication process may be adjusted to provide for two or more mid-purge distribution zones that are distributed at various locations along the length of the adsorbent bed. For example, two mid-purge distribution zones may be utilized with a first mid-purge distribution zone being disposed between a first portion of the adsorbent bed and a second portion of the adsorbent bed and a second mid-purge distribution zone being disposed between a third portion of the adsorbent bed and the second portion of the adsorbent bed. In this configuration, two portions of the contactors (e.g., the first portion and the third portion) may be fabricated as noted above, while the second potion may be fabricated of adsorbent material, as noted above, as well. Alternatively, the inlet conduit may include additional passages, such as divider or another conduit disposed within the purge inlet conduit. For this configuration, a first passage may be distributed between the first and second portions, while the second passage may be distributed between the second and third portions. Similar techniques may be utilized to provide three or more mid-purge distribution zones, which may even combine the above techniques.
In one or more embodiments, the adsorbent bed unit may be utilized to separate contaminants from a feed stream. The method may include 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; interrupting the flow of the gaseous feed stream; performing a depressurization step, wherein the depressurization step reduces the pressure within the adsorbent bed unit; performing a purge step, wherein the purge step reduces the pressure within the adsorbent bed unit and wherein the purge step involves passing a purge stream to a mid-purge distribution zone between first portion and the second portion; 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. Further the method may include that the mid-purge distribution zone is positioned at a location that is between 10% and 60% of the length of the adsorbent bed; that the mid-purge distribution zone is positioned at a location that is between 20% and 40% of the length of the adsorbent bed; the further step of passing the purge stream through a distribution zone in a plenum closure component disposed upstream of the first portion prior to passing the purge stream to the mid-purge distribution zone via at least one gas purge inlet conduit; and the further step of passing the product stream through a primary fluid zone in a plenum closure component disposed upstream of the first portion, wherein the product stream isolates direct fluid communication between the distribution zone and the primary fluid zone.
Further, in one or more embodiments, the adsorbent bed unit may include an adsorbent bed that can be used for the separation of a target gas form a gaseous mixture. The adsorbent is usually comprised of an adsorbent material supported on a non-adsorbent support, or contactor. Such contactors contain substantially parallel flow channels wherein 20 volume percent, preferably 15 volume percent or less of the open pore volume of the contactor, excluding the flow channels, is in pores greater than about 20 angstroms. A flow channel is taken to be that portion of the contactor in which gas flows, if a steady state pressure difference is applied between the point or place at which a feed stream enters the contactor and the point or place at which a product stream leaves the contactor. In the contactor, the adsorbent is incorporated into the wall of the flow channel.
Non-limiting examples of adsorbent materials that can be used with the method and system include high surface area (>10 m2/gm and preferably >75 m2/gm) alumina, microporous zeolites (preferably zeolites with particle sizes <1 mm), other microporous materials, mesoporous materials and ordered mesoporous materials. Nonlimiting examples of these materials include carbons, cationic zeolites, high silica zeolites, highly siliceous ordered mesoporous materials, sol gel materials, ALPO materials (microporous and mesoporous materials containing predominantly aluminum phosphorous and oxygen), SAPO materials (microporous and mesoporous materials containing predominantly silicon aluminum phosphorous and oxygen), MOF materials microporous and mesoporous materials comprised of a metal organic framework) and 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 and other non protogenic basic groups such as amidines, guanidines and biguanides.
In one or more embodiments, the swing adsorption process using the polygon thermal contactors of the present techniques is a temperature swing adsorption (TSA) or a rapid cycle temperature swing adsorption (RCTSA). For TSA the total cycle times are typically less than 12 hours, preferably less than 8 hours, preferably less than 6 hours, preferably less than 4 hours. For RCTSA the total cycle times are typically less than 600 seconds, preferably less than 200 seconds, more preferably less than 100 seconds, and even more preferably less than 60 seconds.
Adsorptive kinetic separation processes, apparatus, and systems, as described above, are useful for development and production of hydrocarbons, such as gas and oil processing. Particularly, the provided processes, apparatus, and systems are useful for the rapid, large scale, efficient separation of a variety of target gases from gas mixtures. In particular, the processes, apparatus, and systems may be used to prepare natural gas products by removing contaminants and heavy hydrocarbons, i.e., hydrocarbons having at least two carbon atoms. The provided processes, apparatus, and systems are useful for preparing gaseous feed streams for use in utilities, including separation applications such as dew point control, sweetening/detoxification, corrosion protection/control, dehydration, heating value, conditioning, and purification. Examples of utilities that utilize one or more separation applications include generation of fuel gas, seal gas, non-potable water, blanket gas, instrument and control gas, refrigerant, inert gas, and hydrocarbon recovery. Exemplary “not to exceed” product (or “target”) gas specifications include: (a) 2 volume percent (vol. %) CO2, 4 parts per million (ppm) H2S, (b) 50 ppm CO2, 4 ppm H2S, or (c) 1.5 vol. % CO2, 2 ppm H2S.
The provided processes, apparatus, and systems may be used to remove acid gas from hydrocarbon streams. Acid gas removal technology may be useful for gas reserves that exhibit higher concentrations of acid gas, i.e., sour gas resources. Hydrocarbon feed streams vary widely in amount of acid gas, such as from several parts per million acid gas to 90 vol. % acid gas. Non-limiting examples of acid gas concentrations from exemplary gas reserves include concentrations of at least: (a) 1 vol. % H2S, 5 vol. % CO2, (b) 1 vol. % H2S, 15 vol. % CO2, (c) 1 vol. % H2S, 60 vol. % CO2, (d) 15 vol. % H2S, 15 vol. % CO2, and (e) 15 vol. % H2S, 30 vol. % CO2.
In one or more embodiments, the streams provided to the adsorbent bed and removed from an adsorbent bed may have different compositions. For example, the hydrocarbon containing stream may have greater than 0.005 volume percent CO2 based on the total volume of the gaseous feed stream and an adsorbent material in the adsorbent bed has a higher selectivity to CO2 as compared to hydrocarbons. Also, the product stream may have greater than 98 volume percent hydrocarbons based on the total volume of the product stream. Further, the gaseous feed stream may be a hydrocarbon containing stream having greater than 20 volume percent CO2 based on the total volume of the gaseous containing stream.
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 preferred examples of the invention and should not be taken as limiting the scope of the invention.
This application claims the priority benefit of U.S. Patent Application 62/162,186 filed May 15, 2015 entitled APPARATUS AND SYSTEM FOR SWING ADSORPTION PROCESSES RELATED THERETO, the entirety of which is incorporated by reference herein.
Number | Name | Date | Kind |
---|---|---|---|
1868138 | Fisk | Jul 1932 | A |
3103425 | Meyer | Sep 1963 | A |
3124152 | Payne | Mar 1964 | A |
3142547 | Marsh | Jul 1964 | A |
3365859 | Sandberg | Jan 1968 | A |
3436839 | Ellington | Apr 1969 | A |
3508758 | Strub | Apr 1970 | 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 |
4321069 | Ritter | Mar 1982 | A |
4324565 | Benkmann | Apr 1982 | A |
4325565 | Winchell | Apr 1982 | A |
4326858 | Benkmann | Apr 1982 | A |
4329162 | Pitcher | May 1982 | A |
4340398 | Doshi et al. | Jul 1982 | A |
4386947 | Mizuno et al. | Jun 1983 | A |
4445441 | Tanca | May 1984 | A |
4461630 | Cassidy et al. | Jul 1984 | A |
4496376 | Hradek | Jan 1985 | A |
4705627 | Miwa et al. | Nov 1987 | A |
4711968 | Oswald et al. | Dec 1987 | A |
4737170 | Searle | Apr 1988 | A |
4770676 | Sircar et al. | 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 |
5104426 | Yamada | Apr 1992 | 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 |
5447558 | Acharya | Sep 1995 | 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 |
5755857 | Acharya | May 1998 | A |
5766311 | Ackley et al. | Jun 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 |
5906673 | Reinhold, III et al. | May 1999 | A |
5914455 | Jain | Jun 1999 | A |
5924307 | Nenov | Jul 1999 | A |
5930910 | Trapp et al. | Aug 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 |
6099621 | Ho | Aug 2000 | A |
6129780 | Millet et al. | Oct 2000 | A |
6136222 | Friesen et al. | Oct 2000 | A |
6147126 | DeGeorge et al. | Nov 2000 | A |
6171371 | Derive et al. | Jan 2001 | B1 |
6176897 | Keefer | Jan 2001 | B1 |
6179900 | Behling et al. | Jan 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 |
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 |
6451095 | Keefer et al. | Sep 2002 | B1 |
6457485 | Hill et al. | Oct 2002 | B2 |
6471939 | Boix et al. | Oct 2002 | B1 |
6488747 | Keefer et al. | Dec 2002 | B1 |
6497750 | Butwell et al. | Dec 2002 | B2 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
8715617 | Genkin et al. | May 2014 | B2 |
8752390 | Wright 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 |
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 |
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 |
9067168 | Frederick et al. | 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 |
9168485 | Deckman et al. | Oct 2015 | B2 |
20010047824 | Hill et al. | Dec 2001 | 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 |
20030170527 | Finn et al. | Sep 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 |
20040197596 | Connor et al. | Oct 2004 | A1 |
20040232622 | Gozdawa | Nov 2004 | A1 |
20050014511 | Spain | Jan 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 |
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 |
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 et al. | Sep 2007 | A1 |
20070253872 | Keefer et al. | Nov 2007 | A1 |
20070261557 | Gadkaree et al. | 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 |
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 |
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 |
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 |
20100326272 | Asaro et al. | Dec 2010 | A1 |
20110002818 | Tonkovich 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 |
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 |
20120011887 | Nakamura | Jan 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 |
20120308456 | Leta et al. | Dec 2012 | A1 |
20120312163 | Leta et al. | Dec 2012 | A1 |
20130061755 | Frederick et al. | Mar 2013 | A1 |
20130068101 | Knapp et al. | Mar 2013 | A1 |
20130225898 | Sundaram et al. | Aug 2013 | A1 |
20140013955 | Tammera et al. | Jan 2014 | A1 |
20140060326 | Sundaram et al. | Mar 2014 | A1 |
20140157986 | Ravikovitch et al. | Jun 2014 | A1 |
20140208797 | Kelley et al. | Jul 2014 | A1 |
20140216254 | Tammera et al. | Aug 2014 | A1 |
20140271394 | Jiang et al. | Sep 2014 | A1 |
20150196870 | Albright et al. | Jul 2015 | A1 |
Number | Date | Country |
---|---|---|
2297590 | Sep 2000 | CA |
2297591 | Sep 2000 | CA |
2224471 | Oct 2000 | CA |
2234924 | Dec 2001 | CA |
2237103 | Dec 2001 | CA |
2228206 | Jan 2002 | CA |
2357356 | Nov 2005 | CA |
2616701 | Feb 2007 | CA |
2423178 | Apr 2013 | CA |
102009003610 | Nov 2009 | DE |
0225736 | Jun 1987 | EP |
0257493 | Feb 1988 | EP |
0262934 | Apr 1988 | EP |
0426937 | May 1991 | EP |
1004341 | May 2000 | EP |
1018359 | Jul 2000 | EP |
1413348 | Aug 2002 | EP |
1 459 799 | Sep 2004 | EP |
1577561 | Sep 2005 | EP |
1203610 | Dec 2005 | EP |
1674555 | Jun 2006 | EP |
1798197 | Jun 2007 | EP |
1045728 | Nov 2009 | EP |
2823872 | Jan 2015 | EP |
2924951 | Jun 2009 | FR |
2013101 | Aug 1979 | GB |
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 |
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 |
WO1999043418 | Sep 1999 | WO |
WO2000035560 | Jun 2000 | WO |
WO2002024309 | Mar 2002 | WO |
WO2002073728 | Sep 2002 | WO |
WO2003031328 | Apr 2003 | WO |
WO2005032694 | Apr 2005 | WO |
WO2005070518 | Aug 2005 | WO |
WO2005090793 | Sep 2005 | WO |
WO2006017940 | Feb 2006 | WO |
WO2006074343 | Jul 2006 | WO |
WO2007111738 | Oct 2007 | WO |
WO2008143967 | Nov 2008 | WO |
WO2009003171 | Dec 2008 | WO |
WO2009003174 | Dec 2008 | WO |
WO2010081809 | Jul 2010 | WO |
WO2010123598 | Oct 2010 | WO |
WO2011139894 | Nov 2011 | WO |
Entry |
---|
Conviser, S. A. (1964) “Removal of CO2 from Natural Gas With Molecular Sieves,” Proceedings of the Gas Conditioning Conf. Univ. of Oklahoma, pp. 1F-12F. |
ExxonMobil Research and Engineering and Xebec (2008) RCPSA-Rapid Cycle Pressure Swing Adsorption—An Advanced, Low-Cost Commercialized H2 Recovery Process, Brochure, 2 pages. |
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. |
Farooq, S. et al. (1990) “Continuous Contercurrent 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. |
GE Oil & Gas (2007) “Dry Gas Seal Retrofit,” Florene, Italy, www.ge.com/oilandgas, 4 pgs. |
Hopper, B. et al. (2008) “World's First 10,000 psi Sour Gas Injection Compressor,” Proceedings of the 37th Turbomachinery Symosium, pp. 73-95. |
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. |
Rameshni, Mahin “Strategies for Sour Gas Field Developments,” Worley Parsons-Brochure, 20 pgs. |
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. |
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 Realiability in Centrifugal Compressors,” Dresser-Rand, Tech. Paper 134, 15 pages. |
Suzuki, M. (1985) “Continuous-Countercurrent-Flow Approximation for Dynamic Steady State Profile of Pressure Swing Adsorption” AIChE Symp. Ser. v81 (242) pp. 67-73. |
Number | Date | Country | |
---|---|---|---|
20160332105 A1 | Nov 2016 | US |
Number | Date | Country | |
---|---|---|---|
62162186 | May 2015 | US |