Fields of Disclosure
The disclosure relates generally to the field of fluid separation. More specifically, the disclosure relates to the cryogenic separation of contaminants, such as acid gas, from a hydrocarbon.
Description of Related Art
This section is intended to introduce various aspects of the art, which may be associated with the present disclosure. This discussion is intended to provide a framework to facilitate a better understanding of particular aspects of the present disclosure. Accordingly, it should be understood that this section should be read in this light, and not necessarily as admissions of prior art.
The production of natural gas hydrocarbons, such as methane and ethane, from a reservoir oftentimes carries with it the incidental production of non-hydrocarbon gases. Such gases include contaminants, such as at least one of carbon dioxide (“CO2”), hydrogen sulfide (“H2S”), carbonyl sulfide, carbon disulfide and various mercaptans. When a feed stream being produced from a reservoir includes these contaminants mixed with hydrocarbons, the stream is oftentimes referred to as “sour gas.”
Many natural gas reservoirs have relatively low percentages of hydrocarbons and relatively high percentages of contaminants. Contaminants may act as a diluent and lower the heat content of hydrocarbons. Some contaminants, like sulfur-bearing compounds, are noxious and may even be lethal. Additionally, in the presence of water some contaminants can become quite corrosive.
It is desirable to remove contaminants from a stream containing hydrocarbons to produce sweet and concentrated hydrocarbons. Specifications for pipeline quality natural gas typically call for a maximum of 2-4% CO2 and ¼ grain H2S per 100 scf (4 ppmv) or 5 mg/Nm3 H2S. Specifications for lower temperature processes such as natural gas liquefaction plants or nitrogen rejection units typically require less than 50 ppm CO2.
The separation of contaminants from hydrocarbons is difficult and consequently significant work has been applied to the development of hydrocarbon/contaminant separation methods. These methods can be placed into three general classes: absorption by solvents (physical, chemical and hybrids), adsorption by solids, and distillation.
Separation by distillation of some mixtures can be relatively simple and, as such, is widely used in the natural gas industry. However, distillation of mixtures of natural gas hydrocarbons, primarily methane, and one of the most common contaminants in natural gas, carbon dioxide, can present significant difficulties. Conventional distillation principles and conventional distillation equipment are predicated on the presence of only vapor and liquid phases throughout the distillation tower. The separation of CO2 from methane by distillation involves temperature and pressure conditions that result in solidification of CO2 if a pipeline or better quality hydrocarbon product is desired. The required temperatures are cold temperatures typically referred to as cryogenic temperatures.
Certain cryogenic distillations can overcome the above mentioned difficulties. These cryogenic distillations provide the appropriate mechanism to handle the formation and subsequent melting of solids during the separation of solid-forming contaminants from hydrocarbons. The formation of solid contaminants in equilibrium with vapor-liquid mixtures of hydrocarbons and contaminants at particular conditions of temperature and pressure takes place in a controlled freeze zone section.
The solid contaminants formed in the controlled freeze zone section fall into a liquid of the controlled freeze zone section that is held above the melting point of the solid contaminants. The liquid is held at a sufficiently warm temperature to melt the solid contaminants. The liquid is part of a melt tray assembly of the controlled freeze zone section. To ensure that all of the solid contaminants melt in the liquid and none exit the controlled freeze zone section and/or plug a liquid discharge line, there needs to be sufficient warm liquid thermal mass in the controlled freeze zone section. In other words, the liquid in the melt tray assembly needs to at least be at a predetermined liquid level.
Liquid level indicators, such as differential pressure cells, guided wave radar sensors and a nucleonic mechanism have been used to help determine the liquid level, but these indicators have disadvantages. Differential pressure cells do not work well in determining the liquid level if the solid contaminants plug the differential pressure cells or associated pressure taps. Guided wave radar sensors do not work well because the temperature and pressure of the controlled freeze zone section is too close to the critical conditions of liquid and vapor, thereby making liquid and vapor nearly indistinguishable. Furthermore, compositional and pressure changes of the stream can cause changes in fluid density, making measurements inconsistent over time. The nucleonic mechanism does not work well in the presence of unsteady amounts of solids.
A need exists for improved technology that maintains at least a predetermined liquid level in a distillation tower so that a minimum warm liquid thermal mass is provided to reliably melt all solid contaminants in the liquid of the melt tray assembly and so that plugging of the controlled freeze zone section liquid discharge is avoided.
The present disclosure provides a device and method for separating contaminants from hydrocarbons, among other things.
A distillation tower may comprise a stripper section constructed and arranged to separate a feed stream at a temperature and pressure at which the feed stream forms no solid; a controlled freeze zone section constructed and arranged to separate the feed stream at a temperature and pressure at which the feed stream forms a solid; a melt tray assembly in the controlled freeze zone section that includes a liquid; an underflow weir in the controlled freeze zone section that alters a flow of the liquid in the melt tray assembly; an overflow weir in the controlled freeze zone section that works with the underflow weir to alter the flow of the liquid in the melt tray assembly and is adjacent to the underflow weir; and a covering element in the controlled freeze zone section that is connected to and extends from the underflow weir.
A method of maintaining a liquid level in a distillation tower may comprise forming a freezing zone vapor stream from a feed stream in a stripper section of a distillation tower at a temperature and pressure at which no solid forms in the stripper section; forming a solid in a controlled freeze zone section of the distillation tower from the feed stream; and maintaining a predetermined liquid level of liquid in a melt tray assembly of the controlled freeze zone section by: altering a flow of the liquid in the melt tray assembly such that the liquid flows from a bottom melt tray assembly portion of the melt tray assembly to a top melt tray assembly portion of the melt tray assembly; and altering the flow of the liquid in the melt tray assembly such that the liquid flows from the top melt tray assembly portion toward the stripper section.
A method for producing hydrocarbons may comprise forming a freezing zone vapor stream from a feed stream in a stripper section of a distillation tower at a temperature and pressure at which no solid forms in the stripper section; forming a solid in a controlled freeze zone section of the distillation tower from the feed stream; maintaining a predetermined liquid level of liquid in a melt tray assembly of the controlled freeze zone section by: altering a flow of the liquid in the melt tray assembly such that the liquid flows from a bottom melt tray assembly portion of the melt tray assembly to a top melt tray assembly portion of the melt tray assembly; and altering the flow of the liquid in the melt tray assembly such that the liquid flows from the top melt tray assembly portion toward the stripper section; and producing hydrocarbons from the feed stream.
The foregoing has broadly outlined the features of the present disclosure in order that the detailed description that follows may be better understood. Additional features will also be described herein.
These and other features, aspects and advantages of the disclosure will become apparent from the following description, appending claims and the accompanying drawings, which are briefly described below.
It should be noted that the figures are merely examples and no limitations on the scope of the present disclosure are intended thereby. Further, the figures are generally not drawn to scale, but are drafted for purposes of convenience and clarity in illustrating various aspects of the disclosure.
For the purpose of promoting an understanding of the principles of the disclosure, reference will now be made to the features illustrated in the drawings and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the disclosure is thereby intended. Any alterations and further modifications, and any further applications of the principles of the disclosure as described herein are contemplated as would normally occur to one skilled in the art to which the disclosure relates. It will be apparent to those skilled in the relevant art that some features that are not relevant to the present disclosure may not be shown in the drawings for the sake of clarity.
As referenced in this application, the terms “stream,” “gas stream,” “vapor stream,” and “liquid stream” refer to different stages of a feed stream as the feed stream is processed in a distillation tower that separates methane, the primary hydrocarbon in natural gas, from contaminants. Although the phrases “gas stream,” “vapor stream,” and “liquid stream,” refer to situations where a gas, vapor, and liquid is mainly present in the stream, respectively, there may be other phases also present within the stream. For example, a gas may also be present in a “liquid stream.” In some instances, the terms “gas stream” and “vapor stream” may be used interchangeably.
The disclosure relates to a system and method for separating a feed stream in a distillation tower. The system and method maintains a predetermined liquid level in the controlled freeze zone section.
The system and method may separate a feed stream having methane and contaminants. The system may comprise a distillation tower 104, 204 (
The distillation tower 104, 204 may be separated into three functional sections: a lower section 106, a middle controlled freeze zone section 108 and an upper section 110. The distillation tower 104, 204 may incorporate three functional sections when the upper section 110 is needed and/or desired.
The distillation tower 104, 204 may incorporate only two functional sections when the upper section 110 is not needed and/or desired. When the distillation tower does not include an upper section 110, a portion of vapor leaving the middle controlled freeze zone section 108 may be condensed in a condenser 122 and returned as a liquid stream via a spray assembly 129. Moreover, lines 18 and 20 may be eliminated, elements 124 and 126 may be one and the same, and elements 150 and 128 may be one and the same. The stream in line 14, now taking the vapors leaving the middle controlled freeze section 108, directs these vapors to the condenser 122.
The lower section 106 may also be referred to as a stripper section. The middle controlled section 108 may also be referred to as the controlled freeze zone section. The upper section 110 may also be referred to as a rectifier section.
The sections of the distillation tower 104 may be housed within a single vessel (
The sections of the distillation tower 204 may be housed within a plurality of vessels to form a split-tower configuration (
The split-tower configuration may be beneficial in situations where the height of the distillation tower, motion considerations, and/or transportation issues, such as for remote locations, need to be considered. This split-tower configuration allows for the independent operation of one or more sections. For example, when the upper section is housed within a single vessel and the lower and middle controlled freeze zone sections are housed within a single vessel, independent generation of reflux liquids using a substantially contaminant-free, largely hydrocarbon stream from a packed gas pipeline or an adjacent hydrocarbon line, may occur in the upper section. And the reflux may be used to cool the upper section, establish an appropriate temperature profile in the upper section, and/or build up liquid inventory at the bottom of the upper section to serve as an initial source of spray liquids for the middle controlled freeze zone section. Moreover, the middle controlled freeze zone and lower sections may be independently prepared by chilling the feed stream, feeding it to the optimal location be that in the lower section or in the middle controlled freeze zone section, generating liquids for the lower and the middle controlled freeze zone sections, and/or disposing the vapors off the middle controlled freeze zone section while they are off specification with too high a contaminant content. Also, liquid from the upper section may be intermittently or continuously sprayed, building up liquid level in the bottom of the middle controlled freeze zone section and bringing the contaminant content in the middle controlled freeze zone section down and near steady state level so that the two vessels may be connected to send the vapor stream from the middle controlled freeze zone section to the upper section, continuously spraying liquid from the bottom of the upper section into the middle controlled freeze zone section and stabilizing operations into steady state conditions. The split tower configuration may utilize a sump of the upper section as a liquid receiver for the pump 128, therefore obviating the need for a liquid receiver 126 in
The system may also include a heat exchanger 100 (
The system may include an expander device 102 (
The system may include a feed separator 103 (
The system may include a dehydration unit 261 (
The system may include a filtering unit (not shown). The feed stream 10 may enter the filtering unit before entering the distillation tower 104, 204. The filtering unit may remove undesirable contaminants from the feed stream before the feed stream enters the distillation tower 104, 204. Depending on what contaminants are to be removed, the filtering unit may be before or after the dehydration unit 261 and/or before or after the heat exchanger 100.
The system may include a line 12 (
If the system includes the feed separator 103 (
The lower section 106 is constructed and arranged to separate the feed stream 10 into an enriched contaminant bottom liquid stream (i.e., liquid stream) and a freezing zone vapor stream (i.e., vapor stream), 301. The lower section 106 separates the feed stream at a temperature, pressure, and/or composition at which no solids form. The liquid stream may comprise a greater quantity of contaminants than of methane. The vapor stream may comprise a greater quantity of methane than of contaminants. In any case, the vapor stream is lighter than the liquid stream. As a result, the vapor stream rises from the lower section 106 and the liquid stream falls to the bottom of the lower section 106.
The lower section 106 may include and/or connect to equipment that separates the feed stream. The equipment may comprise any suitable equipment for separating methane from contaminants, such as one or more packed sections 181, or one or more distillation trays with perforations, downcomers and weirs (
The equipment may include components that apply heat to the stream to form the vapor stream and the liquid stream. For example, the equipment may comprise a first reboiler 112 that applies heat to the stream. The first reboiler 112 may be located outside of the distillation tower 104, 204. The equipment may also comprise a second reboiler 172 that applies heat to the stream. The second reboiler 172 may be located outside of the distillation tower 104, 204. Line 117 may lead from the distillation tower to the second reboiler 172. Line 17 may lead from the second reboiler 172 to the distillation tower. Additional reboilers, set up similarly to the second reboiler described above, may also be used.
The first reboiler 112 may apply heat to the liquid stream that exits the lower section 106 through a liquid outlet 160 of the lower section 106. The liquid stream may travel from the liquid outlet 160 through line 28 to reach the first reboiler 112 (
The first reboiler 112 may also apply heat to the stream within the distillation tower 104, 204. Specifically, the heat applied by the first reboiler 112 warms up the lower section 106. This heat travels up the lower section 106 and supplies heat to warm solids entering a melt tray assembly 139 (
The second reboiler 172 applies heat to the stream within the lower section 106. This heat is applied closer to the middle controlled freeze zone section 108 than the heat applied by the first reboiler 112. As a result, the heat applied by the second reboiler 172 reaches the middle controlled freeze zone section 108 faster than the heat applied by the first reboiler 112. The second reboiler 172 also helps with energy integration.
The equipment may include one or more chimney assemblies 135 (
Each chimney assembly 135 includes a chimney tray 131 that collects the liquid stream within the lower section 106. The liquid stream that collects on the chimney tray 131 may be fed to the second reboiler 172. After the liquid stream is heated in the second reboiler 172, the stream may return to the middle controlled freeze zone section 106 to supply heat to the middle controlled freeze zone section 106 and/or the melt tray assembly 139. Unvaporized stream exiting the second reboiler 172 may be fed back to the distillation tower 104, 204 below the chimney tray 131. Vapor stream exiting the second reboiler 172 may be routed under or above the chimney tray 131 when the vapor stream enters the distillation tower 104, 204.
The chimney tray 131 may include one or more chimneys 137. The chimney 137 serves as a channel that the vapor stream in the lower section 106 traverses. The vapor stream travels through an opening in the chimney tray 131 at the bottom of the chimney 137 to the top of the chimney 137. The opening is closer to the bottom of the lower section 106 than it is to the bottom of the middle controlled freeze zone section 108. The top is closer to the bottom of the middle controlled freeze zone section 108 than it is to the bottom of the lower section 106.
Each chimney 137 has attached to it a chimney cap 133. The chimney cap 133 covers a chimney top opening 138 of the chimney 137. The chimney cap 133 prevents the liquid stream from entering the chimney 137. The vapor stream exits the chimney assembly 135 via the chimney top opening 138.
After falling to the bottom of the lower section 106, the liquid stream exits the distillation tower 104, 204 through the liquid outlet 160. The liquid outlet 160 is within the lower section 106 (
After exiting through the liquid outlet 160, the feed stream may travel via line 28 to the first reboiler 112. The feed stream may be heated by the first reboiler 112 and vapor may then re-enter the lower section 106 through line 30. Unvaporized liquid may continue out of the distillation process via line 24.
The system may include an expander device 114 (
The system may include a heat exchanger 116 (
The vapor stream in the lower section 106 rises from the lower section 106 to the middle controlled freeze zone section 108. The middle controlled freeze zone section 108 is constructed and arranged to separate the feed stream 10 introduced into the middle controlled freeze zone section, or into the top of lower section 106, into a solid and a vapor stream. The solid may be comprised more of contaminants than of methane. The vapor stream (i.e., methane-enriched vapor stream) may comprise more methane than contaminants. The middle controlled freeze zone section 108 operates at least one of a temperature, pressure and composition at which the feed stream forms the solid and the vapor stream 302 (
The middle controlled freeze zone section 108 includes a lower section 40 and an upper section 39 (
The middle controlled freeze zone section 108 may comprise a melt tray assembly 139 that is maintained in the middle controlled freeze zone section 108 (
The melt tray assembly 139 is constructed and arranged to melt solids formed in the middle controlled freeze zone section 108. When the warm vapor stream rises from the lower section 106 to the middle controlled freeze zone section 108, the vapor stream immediately encounters the melt tray assembly 139 and supplies heat to melt the solids. The melt tray assembly 139 may comprise at least one of a melt tray 118, a bubble cap 132, a liquid 130 and heat mechanism(s) 134.
The melt tray 118 may collect a liquid and/or slurry mix. The melt tray 118 divides at least a portion of the middle controlled freeze zone section 108 from the lower section 106. Consequently, the melt tray 118 is at the bottom 45 of the middle controlled freeze zone section 108.
One or more bubble caps 132 may act as a channel for the vapor stream rising from the lower section 106 to the middle controlled freeze zone section 108. The bubble cap 132 may provide a path for the vapor stream up the riser 140 and then down and around the riser 140 to the melt tray 118. The riser 140 is covered by a cap 141. The cap 141 prevents the liquid 130 from travelling into the riser and it also helps prevent solids from travelling into the riser 140. The vapor stream's traversal through the bubble cap 132 allows the vapor stream to transfer heat to the liquid 130 within the melt tray assembly 139.
One or more heat mechanisms 134 may further heat up the liquid 130 to facilitate melting of the solids into a liquid and/or slurry mix. The heat mechanism(s) 134 may be located anywhere within the melt tray assembly 139. For example, as shown in
The liquid 130 in the melt tray assembly is heated by the vapor stream. The liquid 130 may also be heated by the one or more heat mechanisms 134. The liquid 130 helps melt the solids formed in the middle controlled freeze zone section 108 into a liquid and/or slurry mix. Specifically, the heat transferred by the vapor stream heats up the liquid, thereby enabling the heat to melt the solids.
The liquid 130 accumulates in the melt tray assembly 139. The liquid 130 rises to reach a certain liquid level 217. For all of the solids to melt, the liquid level 217 needs to at least be equal to a predetermined liquid level. The predetermined liquid level is one that provides a sufficient warm thermal mass to reliably melt all solids. When the liquid level is at least at this predetermined liquid level, it is more likely that the middle controlled freeze zone section 108 will operate properly by forming solids and vapors and melting the solids in the melt tray assembly 139, such that the methane in the feed stream is separated out from the contaminants in the feed stream.
The middle controlled freeze zone section 108 may also comprise an underflow weir 216 and an overflow weir 215 (
Without both an overflow weir 215 and an underflow weir 216, solids and/or colder liquid may fall from the middle controlled freeze zone section 108 to the lower section 106, thereby preventing adequate separation of the feed stream. The solids may fall, for example, if the middle controlled freeze zone section 108 only includes an overflow weir 215 because solids may fall between the overflow weir 215 and a controlled freeze zone wall 46 of the middle controlled freeze zone section 108. The colder liquid may fall, for example, because the colder liquid is at the top of the melt tray assembly 139 and, therefore, the most likely to travel over the overflow weir 216 and down to the bottom distillation section 106. The warmer liquid, which is what is most desired to fall to the bottom distillation section 106, is at the bottom of the melt tray assembly 139.
With both the overflow weir 215 and the underflow weir 216, the warmer liquid at the bottom of the melt tray assembly 139 flows to the bottom distillation section 106. The underflow weir 216 alters the flow of the liquid such that the liquid flows from a melt tray assembly bottom portion 230 of the melt tray assembly 139 to a melt tray assembly top portion 231 of the melt tray assembly 139, 304 (
When the warmer liquid travels between the overflow weir 215 and the controlled freeze zone wall 46 the warmer liquid may directly or indirectly travel from the middle controlled freeze zone section 108 to the lower section 106. A channel 22 (
The channel 22 may comprise an internal channel 22a (
The channel 22 may comprise an external channel 22b. The external channel 22b is outside of the middle controlled freeze zone section 108 and the lower section 106 (
While the above two paragraphs discuss the channel 22 comprising an internal channel 22a or an external channel 22b, the channel 22 could comprise an internal channel 22a and an external channel 22b.
To prevent solids from falling between the overflow weir 215 and the controlled freeze zone wall 46 and undesirably exiting to the lower section 106, the middle controlled freeze zone section 108 may include a covering element 213 (
Vapor may accumulate in the space between the controlled freeze zone wall 46 and the overflow weir 215 when the warm liquid reaches this space. To prevent accumulation of the vapor in the middle controlled freeze zone section 108 while altering the flow of the liquid, the middle controlled freeze zone section 108 may include an anti-vapor lock 214. If the vapor accumulates, it may be stuck between the controlled freeze zone wall 46 and the overflow weir 215 without an anti-vapor lock. The anti-vapor lock may extend from the controlled freeze zone wall 46 to the covering element 213.
The anti-vapor lock 214 may extend from the controlled freeze zone wall 46 to the covering element 213 at an acute angle to the controlled freeze zone wall 46. The anti-vapor lock 214 may be at a suitable angle 295 (
There is a gap 293 (
The underflow weir 216 may comprise a plurality of underflow weirs and/or the overflow weir 215 may comprise a plurality of overflow weirs 215. When the system comprises one or more underflow weirs 216 and/or one or more overflow weirs 215, the weirs may be positioned at any suitable place within the lower portion of the middle controlled freeze zone section 108. For example, one underflow weir 216 and one overflow weir 215 may be on a left side 46a of the controlled freeze zone wall 46 while a second underflow weir 216 and a second overflow weir 215 may be on a right side 46b of the controlled freeze zone wall 46.
In addition to the underflow weir 216 and overflow weir 215, and despite their potential limitations, the middle controlled freeze zone section 108 may comprise a liquid level indicator 212 (
The middle controlled freeze zone section 108 may also comprise a spray assembly 129. The spray assembly 129 cools the vapor stream that rises from the lower section 40. The spray assembly 129 sprays liquid, which is cooler than the vapor stream, on the vapor stream to cool the vapor stream. The spray assembly 129 is within the upper section 39. The spray assembly 129 is not within the lower section 40. The spray assembly 129 is above the melt tray assembly 139. In other words, the melt tray assembly 139 is below the spray assembly 129.
The spray assembly 129 includes one or more spray nozzles 120 (
The liquid sprayed by the spray assembly 129 contacts the vapor stream at a temperature and pressure at which solids form. The liquid may also contact the vapor stream at a composition at which solids form. Solids, containing mainly contaminants, form when the sprayed liquid contacts the vapor stream (
The temperature in the middle controlled freeze zone section 108 cools down as the vapor stream travels from the bottom of the middle controlled freeze zone section 108 to the top of the middle controlled freeze zone section 108. The methane in the vapor stream rises from the middle controlled freeze zone section 108 to the upper section 110. Some contaminants may remain in the methane and also rise. The contaminants in the vapor stream tend to condense or solidify with the colder temperatures and fall to the bottom of the middle controlled freeze zone section 108.
The solids form the liquid and/or slurry mix when in the liquid 130. The liquid and/or slurry mix flows from the middle controlled freeze zone section 108 to the lower distillation section 106. The liquid and/or slurry mix flows from the bottom of the middle controlled freeze zone section 108 to the top of the lower section 106 via a line 22 (
The vapor stream that rises in the middle controlled freeze zone section 108 and does not form solids or otherwise fall to the bottom of the middle controlled freeze zone section 108, rises to the upper section 110. The upper section 110 operates at, at least one of a temperature, a pressure and a composition and contaminant concentration at which no solid forms. The upper section 110 is constructed and arranged to cool the vapor stream to separate the methane from the contaminants. Reflux in the upper section 110 cools the vapor stream. The reflux is introduced into the upper section 110 via line 18. Line 18 may extend to the upper section 110. Line 18 may extend from an outer surface of the distillation tower 104, 204.
After contacting the reflux in the upper section 110, the feed stream forms a vapor stream and a liquid stream. The vapor stream mainly comprises methane. The liquid stream comprises relatively more contaminants. The vapor stream rises in the upper section 110 and the liquid falls to a bottom of the upper section 110.
To facilitate separation of the methane from the contaminants when the stream contacts the reflux, the upper section 110 may include one or more mass transfer devices 176. Each mass transfer device 176 helps separate the methane from the contaminants. Each mass transfer device 176 may comprise any suitable separation device, such as a tray with perforations, or a section of random or structured packing to facilitate contact of the vapor and liquid phases.
After rising, the vapor stream may exit the distillation tower 104, 204 through line 14. The line 14 may emanate from an upper part of the upper section 110. The line 14 may extend from an outer surface of the upper section 110.
From line 14, the vapor stream may enter a condenser 122. The condenser 122 cools the vapor stream to form a cooled stream. The condenser 122 at least partially condenses the stream.
After exiting the condenser 122, the cooled stream may enter a separator 124. The separator 124 separates the vapor stream into liquid and vapor streams. The separator may be any suitable separator that can separate a stream into liquid and vapor streams, such as a reflux drum.
Once separated, the vapor stream may exit the separator 124 as sales product. The sales product may travel through line 16 for subsequent sale to a pipeline and/or condensation to be a liquefied natural gas.
Once separated, the liquid stream may return to the upper section 110 through line 18 as the reflux. The reflux may travel to the upper section 110 via any suitable mechanism, such as a reflux pump 150 (
The liquid stream (i.e., freezing zone liquid stream) that falls to the bottom of the upper section 110 collects at the bottom of the upper section 110. The liquid may collect on tray 183 (
The line 20 and/or outlet 260 connect to a line 41. The line 41 leads to the spray assembly 129 in the middle controlled freeze zone section 108. The line 41 emanates from the holding vessel 126. The line 41 may extend to an outer surface of the middle controlled freeze zone section 110.
The line 20 and/or outlet 260 may directly or indirectly (
It is important to note that the steps depicted in
Disclosed aspects may be used in hydrocarbon management activities. As used herein, “hydrocarbon management” or “managing hydrocarbons” includes hydrocarbon extraction, hydrocarbon production, hydrocarbon exploration, identifying potential hydrocarbon resources, identifying well locations, determining well injection and/or extraction rates, identifying reservoir connectivity, acquiring, disposing of and/or abandoning hydrocarbon resources, reviewing prior hydrocarbon management decisions, and any other hydrocarbon-related acts or activities. The term “hydrocarbon management” is also used for the injection or storage of hydrocarbons or CO2, for example the sequestration of CO2, such as reservoir evaluation, development planning, and reservoir management. The disclosed methodologies and techniques may be used to produce hydrocarbons in a feed stream extracted from, for example, a subsurface region. The feed stream extracted may be processed in the distillation tower 104, 204 and separated into methane and contaminants. The separated methane exits the middle controlled freeze zone section 108 or the upper section 110 of the distillation tower. Some or all of the methane that exits is produced as produced hydrocarbons, 307 (
As utilized herein, the terms “approximately,” “about,” “substantially,” and similar terms are intended to have a broad meaning in harmony with the common and accepted usage by those of ordinary skill in the art to which the subject matter of this disclosure pertains. It should be understood by those of skill in the art who review this disclosure that these terms are intended to allow a description of certain features described and claimed without restricting the scope of these features to the precise numeral ranges provided. Accordingly, these terms should be interpreted as indicating that insubstantial or inconsequential modifications or alterations of the subject matter described and considered to be within the scope of the disclosure.
It should be understood that numerous changes, modifications, and alternatives to the preceding disclosure can be made without departing from the scope of the disclosure. The preceding description, therefore, is not meant to limit the scope of the disclosure. Rather, the scope of the disclosure is to be determined only by the appended claims and their equivalents. It is also contemplated that structures and features in the present examples can be altered, rearranged, substituted, deleted, duplicated, combined, or added to each other.
The articles “the”, “a” and “an” are not necessarily limited to mean only one, but rather are inclusive and open ended so as to include, optionally, multiple such elements.
This application claims the priority benefit of U.S. Patent Application 61/912,959 filed Dec. 6, 2013 entitled METHOD AND SYSTEM OF MAINTAINING A LIQUID LEVEL IN A DISTILLATION TOWER, the entirety of which is incorporated by reference herein. This application is related to but does not claim priority to U.S. Provisional patent application Nos. 61/912,957 filed on Dec. 6, 2013 entitled METHOD AND DEVICE FOR SEPARATING HYDROCARBONS AND CONTAMINANTS WITH A SPRAY ASSEMBLY; 62/044,770 filed on Sep. 2, 2014 entitled METHOD AND DEVICE FOR SEPARATING HYDROCARBONS AND CONTAMINANTS WITH A SPRAY ASSEMBLY; 61/912,964 filed on Dec. 6, 2013 entitled METHOD AND DEVICE FOR SEPARATING A FEED STREAM USING RADIATION DETECTORS; 61/912,970 filed on Dec. 6, 2013 entitled METHOD AND SYSTEM OF DEHYDRATING A FEED STREAM PROCESSED IN A DISTILLATION TOWER; 61/912,975 filed on Dec. 6, 2013 entitled METHOD AND SYSTEM FOR SEPARATING A FEED STREAM WITH A FEED STREAM DISTRIBUTION MECHANISM; 61/912,978 filed on Dec. 6, 2013 entitled METHOD AND SYSTEM FOR PREVENTING ACCUMULATION OF SOLIDS IN A DISTILLATION TOWER; 61/912,983 filed on Dec. 6, 2013 entitled METHOD OF REMOVING SOLDS BY MODIFYING A LIQUID LEVEL IN A DISTILLATION TOWER; 61/912,984 filed on Dec. 6, 2013 entitled METHOD AND SYSTEM OF MODIFYING A LIQUID LEVEL DURING START-UP OPERATIONS; 61/912,986 filed on Dec. 6, 2013 entitled METHOD AND DEVICE FOR SEPARATING HYDROCARBONS AND CONTAMINANTS WITH A HEATING MECHANISM TO DESTABILIZE AND/OR PREVENT ADHESION OF SOLIDS; 61/912,987 filed on Dec. 6, 2013 entitled METHOD AND DEVICE FOR SEPARATING HYDROCARBONS AND CONTAMINANTS WITH A SURFACE TREATMENT MECHANISM.
Number | Name | Date | Kind |
---|---|---|---|
2621216 | White | Dec 1952 | A |
2843219 | Habgood | Jul 1958 | A |
2863527 | Herbert et al. | Dec 1958 | A |
2960837 | Swenson et al. | Nov 1960 | A |
3050950 | Karwat et al. | Aug 1962 | A |
3109726 | Karwat | Nov 1963 | A |
3282576 | Bruckert | Nov 1966 | A |
3349571 | Nebgen | Oct 1967 | A |
3393527 | Swensen et al. | Jul 1968 | A |
3400512 | McKay | Sep 1968 | A |
3421984 | Jensen et al. | Jan 1969 | A |
3683634 | Streich | Aug 1972 | A |
3705625 | Whitten et al. | Dec 1972 | A |
3767766 | Tjoa et al. | Oct 1973 | A |
3824080 | Smith et al. | Jul 1974 | A |
3842615 | Reigel et al. | Oct 1974 | A |
3848427 | Loofbourow | Nov 1974 | A |
3895101 | Tsuruta | Jul 1975 | A |
3929635 | Buriks et al. | Dec 1975 | A |
3933001 | Muska | Jan 1976 | A |
4129626 | Mellbom | Dec 1978 | A |
4246015 | Styring | Jan 1981 | A |
4270937 | Adler | Jun 1981 | A |
4280559 | Best | Jul 1981 | A |
4281518 | Muller et al. | Aug 1981 | A |
4318723 | Holmes et al. | Mar 1982 | A |
4319964 | Katz et al. | Mar 1982 | A |
4336233 | Appl et al. | Jun 1982 | A |
4344485 | Butler | Aug 1982 | A |
4370156 | Goddin et al. | Jan 1983 | A |
4382912 | Madgavkar et al. | May 1983 | A |
4383841 | Ryan et al. | May 1983 | A |
4405585 | Sartori et al. | Sep 1983 | A |
4417449 | Hegarty et al. | Nov 1983 | A |
4417909 | Weltmer | Nov 1983 | A |
4421535 | Mehra | Dec 1983 | A |
4441900 | Swallow | Apr 1984 | A |
4459142 | Goddin | Jul 1984 | A |
4462814 | Holmes et al. | Jul 1984 | A |
4466946 | Goddin et al. | Aug 1984 | A |
4511382 | Valencia et al. | Apr 1985 | A |
4512782 | Bauer et al. | Apr 1985 | A |
4533372 | Valencia et al. | Aug 1985 | A |
4551158 | Wagner et al. | Nov 1985 | A |
4563202 | Yao et al. | Jan 1986 | A |
4592766 | Kumman et al. | Jun 1986 | A |
4602477 | Lucadamo | Jul 1986 | A |
4609388 | Adler et al. | Sep 1986 | A |
4636334 | Skinner et al. | Jan 1987 | A |
4695672 | Bunting | Sep 1987 | A |
4697642 | Vogel | Oct 1987 | A |
4710213 | Sapper et al. | Dec 1987 | A |
4717408 | Hopewell | Jan 1988 | A |
4720294 | Lucadamo et al. | Jan 1988 | A |
4747858 | Gottier | May 1988 | A |
4761167 | Nicholas et al. | Aug 1988 | A |
4762543 | Pantermuehl et al. | Aug 1988 | A |
4769054 | Steigman | Sep 1988 | A |
4822393 | Markbreiter et al. | Apr 1989 | A |
4831206 | Zarchy | May 1989 | A |
4923493 | Valencia et al. | May 1990 | A |
4927498 | Rushmere | May 1990 | A |
4935043 | Blanc et al. | Jun 1990 | A |
4954220 | Rushmere | Sep 1990 | A |
4972676 | Sakai | Nov 1990 | A |
4976849 | Soldati | Dec 1990 | A |
5011521 | Gottier | Apr 1991 | A |
5062270 | Haut et al. | Nov 1991 | A |
5120338 | Potts et al. | Jun 1992 | A |
5137550 | Hegarty et al. | Aug 1992 | A |
5152927 | Rivers | Oct 1992 | A |
5233837 | Callahan | Aug 1993 | A |
5240472 | Sircar | Aug 1993 | A |
5247087 | Rivers | Sep 1993 | A |
5265428 | Valencia | Nov 1993 | A |
5335504 | Durr et al. | Aug 1994 | A |
5345771 | Dinsmore | Sep 1994 | A |
5567396 | Perry et al. | Oct 1996 | A |
5620144 | Strock et al. | Apr 1997 | A |
5643460 | Marble et al. | Jul 1997 | A |
5700311 | Spencer | Dec 1997 | A |
5720929 | Minkkinen et al. | Feb 1998 | A |
5819555 | Engdahl | Oct 1998 | A |
5820837 | Marjanovich et al. | Oct 1998 | A |
5899274 | Frauenfeld et al. | May 1999 | A |
5956971 | Cole et al. | Sep 1999 | A |
5964985 | Wootten | Oct 1999 | A |
5983663 | Sterner | Nov 1999 | A |
6053007 | Victory et al. | Apr 2000 | A |
6053484 | Fan et al. | Apr 2000 | A |
6082133 | Barclay et al. | Jul 2000 | A |
6082373 | Sakurai et al. | Jul 2000 | A |
6162262 | Minkkinen et al. | Dec 2000 | A |
6223557 | Cole | May 2001 | B1 |
6240744 | Agrawal et al. | Jun 2001 | B1 |
6267358 | Gohara et al. | Jul 2001 | B1 |
6270557 | Millet et al. | Aug 2001 | B1 |
6274112 | Moffett et al. | Aug 2001 | B1 |
6287367 | Buchanan | Sep 2001 | B1 |
6336334 | Minkkinen et al. | Jan 2002 | B1 |
6374634 | Gallarda et al. | Apr 2002 | B2 |
6401486 | Lee et al. | Jun 2002 | B1 |
6416729 | DeBerry et al. | Jul 2002 | B1 |
6442969 | Rojey et al. | Sep 2002 | B1 |
6500982 | Hale et al. | Dec 2002 | B1 |
6505683 | Minkkinen et al. | Jan 2003 | B2 |
6516631 | Trebble | Feb 2003 | B1 |
6517801 | Watson et al. | Feb 2003 | B2 |
6539747 | Minta et al. | Apr 2003 | B2 |
6565629 | Hayashida et al. | May 2003 | B1 |
6605138 | Frondorf | Aug 2003 | B2 |
6631626 | Hahn | Oct 2003 | B1 |
6632266 | Thomas et al. | Oct 2003 | B2 |
6662872 | Gutek et al. | Dec 2003 | B2 |
6708759 | Leaute et al. | Mar 2004 | B2 |
6711914 | Lecomte | Mar 2004 | B2 |
6735979 | Lecomte et al. | May 2004 | B2 |
6755251 | Thomas et al. | Jun 2004 | B2 |
6755965 | Pironti et al. | Jun 2004 | B2 |
6818194 | DeBerry et al. | Nov 2004 | B2 |
6883327 | Iijima et al. | Apr 2005 | B2 |
6946017 | Leppin et al. | Sep 2005 | B2 |
6958111 | Rust et al. | Oct 2005 | B2 |
6962061 | Wilding et al. | Nov 2005 | B2 |
7001490 | Wostbrock et al. | Feb 2006 | B2 |
7004985 | Wallace et al. | Feb 2006 | B2 |
7066986 | Haben et al. | Jun 2006 | B2 |
7073348 | Clodic et al. | Jul 2006 | B2 |
7121115 | Lemaire et al. | Oct 2006 | B2 |
7128150 | Thomas et al. | Oct 2006 | B2 |
7128276 | Nilsen et al. | Oct 2006 | B2 |
7152431 | Amin et al. | Dec 2006 | B2 |
7211128 | Thomas et al. | May 2007 | B2 |
7211701 | Muller et al. | May 2007 | B2 |
7219512 | Wilding et al. | May 2007 | B1 |
7285225 | Copeland et al. | Oct 2007 | B2 |
7325415 | Amin et al. | Feb 2008 | B2 |
7424808 | Mak | Sep 2008 | B2 |
7437889 | Roberts et al. | Oct 2008 | B2 |
7442231 | Landrum | Oct 2008 | B2 |
7442233 | Mitariten | Oct 2008 | B2 |
7493779 | Amin | Feb 2009 | B2 |
7536873 | Nohlen | May 2009 | B2 |
7550064 | Bassler et al. | Jun 2009 | B2 |
7575624 | Cartwright et al. | Aug 2009 | B2 |
7597746 | Mak et al. | Oct 2009 | B2 |
7635408 | Mak et al. | Dec 2009 | B2 |
7637984 | Adamopoulos | Dec 2009 | B2 |
7637987 | Mak | Dec 2009 | B2 |
7641717 | Gal | Jan 2010 | B2 |
7662215 | Sparling et al. | Feb 2010 | B2 |
7691239 | Kister et al. | Apr 2010 | B2 |
7722289 | Leone et al. | May 2010 | B2 |
7729976 | Hill et al. | Jun 2010 | B2 |
7770872 | Delatour | Aug 2010 | B2 |
7795483 | Kulprathipanja et al. | Sep 2010 | B2 |
7806965 | Stinson | Oct 2010 | B2 |
7814975 | Hagen et al. | Oct 2010 | B2 |
7879135 | Ravikumar et al. | Feb 2011 | B2 |
7901583 | McColl et al. | Mar 2011 | B2 |
7955496 | Iqbal et al. | Jun 2011 | B2 |
8002498 | Leone et al. | Aug 2011 | B2 |
8020408 | Howard et al. | Sep 2011 | B2 |
8133764 | Dirks et al. | Mar 2012 | B2 |
8136799 | Griepsma | Mar 2012 | B2 |
8303685 | Schubert et al. | Nov 2012 | B2 |
8308849 | Gal | Nov 2012 | B2 |
8312738 | Singh et al. | Nov 2012 | B2 |
8372169 | Tsangaris et al. | Feb 2013 | B2 |
8381544 | Coyle | Feb 2013 | B2 |
8388832 | Moffett et al. | Mar 2013 | B2 |
8428835 | Habert et al. | Apr 2013 | B2 |
8475572 | Prast et al. | Jul 2013 | B2 |
8500105 | Nieuwoudt | Aug 2013 | B2 |
8529662 | Kelley et al. | Sep 2013 | B2 |
20020174687 | Cai | Nov 2002 | A1 |
20020189443 | McGuire | Dec 2002 | A1 |
20030181772 | Meyer et al. | Sep 2003 | A1 |
20060207946 | McColl et al. | Sep 2006 | A1 |
20060239879 | Lallemand et al. | Oct 2006 | A1 |
20070056317 | Amin et al. | Mar 2007 | A1 |
20070144943 | Lemaire et al. | Jun 2007 | A1 |
20070277674 | Hirano et al. | Dec 2007 | A1 |
20080034789 | Fieler et al. | Feb 2008 | A1 |
20080091316 | Szczublewski | Apr 2008 | A1 |
20080092589 | Tranier et al. | Apr 2008 | A1 |
20080150171 | Lee | Jun 2008 | A1 |
20080307827 | Hino et al. | Dec 2008 | A1 |
20090023605 | Lebl et al. | Jan 2009 | A1 |
20090220406 | Rahman | Sep 2009 | A1 |
20100011809 | Mak | Jan 2010 | A1 |
20100018248 | Fieler | Jan 2010 | A1 |
20100024472 | Amin et al. | Feb 2010 | A1 |
20100064725 | Chieng et al. | Mar 2010 | A1 |
20100107687 | Andrian et al. | May 2010 | A1 |
20100132405 | Nilsen | Jun 2010 | A1 |
20100147022 | Hart et al. | Jun 2010 | A1 |
20100187181 | Sortwell | Jul 2010 | A1 |
20100310439 | Brok et al. | Dec 2010 | A1 |
20110132034 | Beaumont et al. | Jun 2011 | A1 |
20110154856 | Andrian et al. | Jun 2011 | A1 |
20110168019 | Northrop et al. | Jul 2011 | A1 |
20110192190 | Andrian et al. | Aug 2011 | A1 |
20110265512 | Bearden et al. | Nov 2011 | A1 |
20120006055 | Van Santen et al. | Jan 2012 | A1 |
20120031143 | Van Santem et al. | Feb 2012 | A1 |
20120031144 | Northrop et al. | Feb 2012 | A1 |
20120079852 | Northrop et al. | Apr 2012 | A1 |
20120125043 | Cullinane et al. | May 2012 | A1 |
20120204599 | Northrop et al. | Aug 2012 | A1 |
20120279728 | Northrop et al. | Nov 2012 | A1 |
20130032029 | Mak | Feb 2013 | A1 |
20130074541 | Kaminsky et al. | Mar 2013 | A1 |
20130098105 | Northrop | Apr 2013 | A1 |
20140137599 | Oelfke et al. | May 2014 | A1 |
Number | Date | Country |
---|---|---|
3149847 | Jul 1983 | DE |
0133208 | Feb 1985 | EP |
0508244 | Oct 1992 | EP |
1338557 | Mar 2005 | EP |
1010403 | Nov 1965 | GB |
WO 0232536 | Apr 2002 | WO |
WO 0239038 | May 2002 | WO |
WO 2004047956 | Jun 2004 | WO |
WO 2008034789 | Mar 2008 | WO |
WO 2008095258 | Aug 2008 | WO |
WO 2008152030 | Dec 2008 | WO |
WO 2009023605 | Feb 2009 | WO |
WO 2009029353 | Mar 2009 | WO |
WO 2009087206 | Jul 2009 | WO |
WO 2010023238 | Mar 2010 | WO |
WO 2010052299 | May 2010 | WO |
WO 2010136442 | Dec 2010 | WO |
WO 2011026170 | Mar 2011 | WO |
WO 2013095828 | Jun 2013 | WO |
WO 2013142100 | Sep 2013 | WO |
Entry |
---|
U.S. Appl. No. 14/516,686, filed Oct. 17, 2014, Valencia, J. A. |
U.S. Appl. No. 14/516,689, filed Oct. 17, 2014, Cullinane, J. T. et al. |
U.S. Appl. No. 14/516,705, filed Oct. 17, 2014, Valencia, J. A. et al. |
U.S. Appl. No. 14/516,709, filed Oct. 17, 2014, Valencia, J. A. |
U.S. Appl. No. 14/516,713, filed Oct. 17, 2014, Valencia, J. A. et al. |
U.S. Appl. No. 14/516,717, filed Oct. 17, 2014, Valencia, J. A. et al. |
U.S. Appl. No. 14/516,718, filed Oct. 17, 2014, Valencia, J. A. |
U.S. Appl. No. 14/516,726, filed Oct. 17, 2014, Valencia, J. A. et al. |
U.S. Appl. No. 14/516,731, filed Oct. 17, 2014, Valencia, J. A. et al. |
Aaron, D. et al. (2005) “Separation of CO2 from Flue Gas: A Review,” Separation Science and Technology, 40, pp. 321-348. |
Amin, R. (2003) “Advanced Mini Natural Gas Liquefier,” LNG Journal, Mar.-Apr. 2003, pp. 20-23. |
Black, S. (2006) “Chilled Ammonia Process for CO2 Capture,” Alstom Position Paper, Nov. 2006, 6 pgs. |
Ciulla, Vincent (2007) “How the Engine Works,” About.com, Mar. 21, 2007, [retrieved from the internet on Aug. 17, 2012]. <URL: http://autorepair.about.com/cs/generalinfo/a/aa060500a.html>. |
“Cryogenics” Science Clarified, May 2, 2006 [retrieved from the internet on Aug. 17, 2012]. <URL: http://www.scienceclarified.com/Co-Di/Cryogenics.html>. |
Denton, R. D. et al. (1985) “Integrated Low Temperature Processing of Sour Natural Gas,” Gas Processors Assoc., 64th Ann. Conv., pp. 92-96. |
Guccione, E. (1963) “New Approach to Recovery of Helium from Natural Gas,” Chem. Engr., Sep. 30, 1963, pp. 76-78. |
Hassan, S. M. N. (2005) “Techno-Economic Study of CO2 Capture Process for Cement Plants,” University of Waterloo—Thesis. |
Haut, R. C. et al. (1988) “Development and Application of the Controlled Freeze Zone Process,” SPE 17757, SPE Gas Tech. Symp.—Dallas, TX, pp. 435-443. |
Haut, R. C. et al. (1988) “Development and Application of the Controlled Freeze Zone Process,” OSEA 88197, 7th Offshore So. East Asia Conf., Singapore, Feb. 1988, pp. 840-848. |
Haut, R. C. et al. (1989) “Development and Application of the Controlled Freeze Zone Process,” SPE Production Engineering, Aug. 1989, pp. 265-271. |
Im, U. K. et al. (1971) “Heterogeneous Phase Behavior of Carbon Dioxide in n-Hexane and n-Heptane at Low Temperatures,” Jrnl. of Chem. Engineering Data, v.16.4, pp. 412-415. |
Mitariten, M. et al. (2007) “The Sorbead™ Quick-Cycle Process for Simultaneous Removal of Water, Heavy Hydrocarbons and Mercaptans from Natural Gas,” Laurance Reid Gas Conditioning Conf., Feb. 25-27, 2007. |
Northrop, P. Scott et al. (2004) “Cryogenic Sour Gas Process Attractive for Acid Gas Injection Applications,” 83rd Ann. Gas Processors Assoc. Convention, New Orleans, LA., pp. 1-8 (XP007912217). |
Pagcatipunan, C. et al. (2005) “Maximize the Performance of Spray Nozzle Systems,” CEP Magazine, Dec. 2005, pp. 38-44. |
Reyes, S. C. et al. (1997) “Frequency Modulation Methods for Diffusion and Adsorption Measurements in Porous Solids,” J. Phys. Chem. B, v.101, pp. 614-622. |
Rubin, E. S. et al. (2002) “A Technical, Economic and Environmental Assessment of Amine-based CO2 Capture Technology for Power Plant Greenhouse Gas Control,” U.S. Dept. of Energy, Oct. 2002, DOE/DE-FC26-00NT40935, 26 pages. |
Spero, C. (2007) “Callide Oxyfuel Project,” CS Energy, cLET Seminar, Jul. 12, 2007, 9 pages. |
Thomas, E. R. et al. (1987) “Conceptual Studies Using the Controlled Freeze Zone (CFZ) Process,” AlChE Summer Nat'l Mtg., Aug. 16-19, 1987. |
Thomas, E. R. et al. (1988) “Conceptual Studies for CO2/Natural Gas Separation Using the Control Freeze Zone (CFZ) Process,” Gas Separation and Purification, v. 2, pp. 84-89. |
Valencia, J. A. et al. (2008) “Controlled Freeze Zone™ Technology for Enabling Processing of High CO2 and H2S Gas Reserves,” SPE-IPTC 12708, Kuala Lumpur, IN, v.4.1, Jan. 2008, pp. 2358-2363. |
Victory, D. J. et al. (1987) “The CFZ Process: Direct Methane-Carbon Dioxide Fractionation,” 66th Ann. GPA Convention, Mar. 16-18, Denver, CO. |
Wilson, R.W. et al. (1968) “Helium: Its Extraction and Purification,” Journ. Petrol. Tech., v. 20, pp. 341-344. |
Number | Date | Country | |
---|---|---|---|
20150159939 A1 | Jun 2015 | US |
Number | Date | Country | |
---|---|---|---|
61912959 | Dec 2013 | US |