Cold membrane nitrogen rejection process and system
11318411 · 2022-05-03
Assignee
Inventors
- Paul TERRIEN (Syracuse, NY, US)
- Alex Augustine (King of Prussia, PA, US)
- Kevin Weatherford (Houston, TX, US)
- Yong Ding (Waban, MA)
Cpc classification
B01D2259/65
PERFORMING OPERATIONS; TRANSPORTING
B01D2317/06
PERFORMING OPERATIONS; TRANSPORTING
International classification
Abstract
An approach for separating a gaseous mixture includes a multi-stage membrane system in which a rubbery membrane is operated at a low temperature. Various streams are cooled and heated in a multi-fluid heat exchanger. In specific configurations, the multi-fluid heat exchanger is cooled by using no fluids other than fluids derived from the permeate and/or residue generated in the first membrane stage.
Claims
1. A membrane separation process, comprising: cooling a natural gas feed containing methane and nitrogen in a main heat exchanger to produce a cooled feed at a temperature below 0° C.; processing the cooled feed in a first membrane stage comprising rubbery membranes to produce a first permeate enriched in methane and a first residue enriched in nitrogen; heating at least a portion of the first residue in the main heat exchanger to produce a heated first residue stream, introducing the heated first residue stream into a second membrane stage comprising rubbery membranes to produce a second permeate enriched in methane and a second residue enriched in nitrogen, heating at least a portion of the first permeate in the main heat exchanger to produce a heated first permeate stream, introducing the heated first permeate stream into a third membrane stage comprising rubbery membranes so as to obtain a third permeate enriched in methane and a third residue enriched in nitrogen, the third permeate being a methane-rich product, and recycling the second permeate back to the first membrane stage.
2. The process of claim 1, wherein no fluids are used to cool the main heat exchanger other than fluids derived from the first permeate and/or fluids derived from the first residue.
3. The process of claim 1, wherein the feed contains at least methane, nitrogen and water, water in the feed is removed in a multi-bed adsorption dryer, and adsorbent in the multi-bed adsorption dryer is regenerated using the second or third residue.
4. The process of claim 1, wherein the the second permeate is warmed in the main heat exchanger before being recycled back to the feed.
5. The process of claim 1, wherein the main heat exchanger is a multi-fluid heat exchanger.
6. The process of claim 1, further comprising the step of heating fluids derived from the second residue in the main heat exchanger.
7. The process of claim 1, further comprising the step of controlling a temperature of the cooled feed via a bypass valve.
8. A membrane separation system, comprising: a source of natural gas comprising methane nitrogen; a feed conduit for directing a flow of feed gas comprising methane and nitrogen; first, second, and third membrane separation stages, each comprising rubbery membranes selective for methane over nitrogen, a feed inlet, a permeate outlet, and a residue outlet, wherein each of the membrane stages is adapted and configured to produce a respective permeate enriched in methane and a respective residue enriched in nitrogen, the feed inlet of the first membrane separation stage is in downstream flow communication with the feed conduit, the feed inlet of the third membrane separation stage is in downstream flow communication with the permeate outlet of the first membrane stage, and the feed inlet of the second membrane separation stage is in downstream flow communication with the residue outlet of the first membrane separation stage; and a multi-fluid heat exchanger, wherein: the first, second, and third membrane separation stages and the multi-fluid heat exchanger are adapted and configured to heat the retentate produced by the first membrane separation stage at the multi-fluid heat exchanger before being fed to the second membrane stage and heat the permeate produced by the first membrane stage at the multi-fluid heat exchanger before being fed to the third membrane stage; and the feed conduit and the multi-fluid heat exchanger are adapted and configured for cooling the flow of feed gas at the multi-fluid heat exchanger.
9. The membrane separation system of claim 8, wherein no fluids are used to cool the main heat exchanger other than fluids derived from the permeate or residue produced by the first membrane stage.
10. The membrane separation system of claim 8, further comprising a bypass valve adapted and configured for controlling a temperature of a cooled feed introduced to the first membrane stage by allowing a portion of the flow of feed gas to bypass the multi-fluid heat exchanger, wherein the portion of the flow of feed gas that bypasses the multi-fluid heat exchanger is combined with a remaining portion of the flow of feed gas that is cooled at the multi-fluid heat exchanger before the combined portions are fed to the first membrane stage.
11. The membrane separation system of claim 8, further comprising a conduit for recycling the second permeate back to the feed that is in downstream fluid communication with the permeate outlet of the second membrane stage and in upstream flow communication with the feed inlet of the first membrane stage.
12. The membrane separation stage of claim 11, further comprising a compressor in fluid communication between the permeate outlet of the second membrane stage and the feed inlet of the first membrane stage.
13. The membrane separation system of claim 8, further comprising a conduit for recycling the permeate from the second membrane stage back to the feed that is in downstream fluid communication with the permeate outlet of the second membrane stage and in upstream flow communication with the feed inlet of the first membrane stage.
14. The membrane separation system of claim 13, further comprising a compressor in fluid communication between the permeate outlet of the second membrane stage and the feed inlet of the first membrane stage and a compressor in downstream fluid communication with the permeate outlet of the third membrane stage.
15. The membrane separation system of claim 8, wherein said system is configured to produce a first permeate having a nitrogen content that is less than 4 times a nitrogen content of the feed.
16. The membrane separation system of claim 8, wherein said system is configured to cool the flow of feed gas to a temperature below 0° C.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) In the accompanying drawings, reference characters refer to the same parts throughout the different views. The drawings are not necessarily to scale; emphasis has instead been placed upon illustrating the principles of the invention. Of the drawings:
(2)
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DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
(6) The invention now will be described more fully hereinafter with reference to the accompanying drawings, in which illustrative embodiments of the invention are shown. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art.
(7) As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. Further, the singular forms and the articles “a”, “an” and “the” are intended to include the plural forms as well, unless expressly stated otherwise. It will be further understood that the terms: includes, comprises, including and/or comprising, when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. Further, it will be understood that when an element, including component or subsystem, is referred to and/or shown as being connected or coupled to another element, it can be directly connected or coupled to the other element or intervening elements may be present.
(8) It will be understood that although terms such as “first” and “second” are used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element from another element. Thus, an element discussed below could be termed a second element, and similarly, a second element may be termed a first element without departing from the teachings of the present invention.
(9) Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.
(10) The invention generally relates to a membrane-based separation process and system. In specific implementations, the separation removes N.sub.2 from a gas mixture. The mixture can consist of, consist essentially of or comprise CH.sub.4 and N.sub.2. Other components that can be present, in addition to CH.sub.4 and N.sub.2, include water vapors, other hydrocarbons (e.g., ethane, propane, butane, pentane, hexane, etc.), carbon dioxide (CO.sub.2), carbon monoxide (CO), hydrogen gas (H.sub.2), helium (He), hydrogen sulfide (H.sub.2S, ammonia (NH.sub.3), etc. Water can be present in any amounts. If liquid water is present it will typically be removed using a gas/liquid separator as a very first step. In cases in which the water content is too high for the process described here, a dehydration system will be included in order to reach a water dew point temperature lower than the lowest temperature encountered in this process (typically a dew point of −20° C. or below).
(11) Examples of mixtures that comprise CH.sub.4 and N.sub.2 include natural gas (such as but not limited to traditional natural gas, shale gas, associated gas) and biogas (such as but not limited to gas from digesters, landfills, etc.). In biogas, N.sub.2/CH.sub.4 ratio can range typically from 0-1% mol (in which case no particular nitrogen removal treatment is required) to 10% mol or more. Natural gas usually contains very small amounts of nitrogen compatible with pipeline specifications but some natural gas fields contain higher amount of nitrogen ranging from a few percent up to close to 100% in some extreme cases. The invention is particularly well suited for biogas and natural gas field with limited amount of nitrogen (typically from 3-4% mol up to 10-15% mol).
(12) Many of the embodiments described herein involve a multi-stage membrane separation process, employing two or more (e.g., three) membranes, also referred to as membrane “stages”. The membranes are selected based on their performance for the desired separation, that of CH.sub.4 and N.sub.2, for instance. Possible membranes that can be employed are provided in U.S. Pat. Nos. 5,669,958 and 6,630,011B1. Membranes having the potential to effect the CH.sub.4—N.sub.2 separation often include rubbery membranes such as those having a rubbery separation layer. Some potential examples of materials that can be employed for the separation layer include poly(dimethyl siloxane) (PDMS), e.g., homopolymers of dimethylsiloxane, and copolymers of dimethyl siloxane with methylethyl siloxane, methyl propyl siloxane, methyl butyl siloxane, methyl pentylsiloxane, methyl hexyl siloane, methyloxtyl siloane, methyl phenyl siloxane. The rubbery material can include block copolymers of dimethylsiloxane or methyloctylsiloxane with polyarylethers, polyamides, polyesters, polyketones, polyimides or block copolymers of dimethyl siloxanes or methyl octyl siloxane with silicates. Another possible material is a ladder-type silicone block copolymer with a general formula of:
HO{[C.sub.6H.sub.5SiO.sub.1.5].sub.n[Si(CH.sub.3).sub.2O].sub.m}H, where n=30-60, m=80-130.
(13) Many implementations described herein utilize a rubbery type membrane that preferentially permeates CH.sub.4, with the retentate representing the N.sub.2-rich fraction. Factors such as the specific membrane material, flat sheet, hollow fiber, etc. configuration, performance characteristics, and so forth, can be selected according to the process to be conducted, size of the operation, feed composition, feed properties, and so forth.
(14) The membrane material and/or membrane attributes in the membrane stages employed can be the same or different.
(15) The separation process and system described herein involves heating and cooling various streams. In specific aspects, the heat exchange between multiple (two or more) streams is conducted in a main heat exchanger, many implementations utilizing a multi-fluid, also referred to herein as a “multi-sided”, heat exchanger, a plate-fin exchanger, e.g., a brazed aluminum heat exchanger (BAHX), for instance.
(16) The main heat exchanger can include various commercially available types, usually custom-designed. It can be configured for counter-flow, cross-flow or various flow combinations and can be optimized with respect to various fin types, surface areas, pressure drops, etc. In many implementations, the heat exchanger is will be preferentially counter-current/counter-flow, as cross-flow or other flow combination may limit the heat recovery possible. For a continuous multi-stage separation process, multiple streams can be heated or cooled simultaneously. The heat exchanger is generally designed for the most challenging case (maximum flow, minimum cold temperature, most challenging composition) and if no particular control is put in place, temperatures will change according to operating cases. A temperature control arrangement can be employed to control the temperatures, using, for example, control valves to bypass some passes in the heat exchanger.
(17) In many embodiments, the heat exchanger is designed to provide more cooling than necessary, while valves bypassing from warm to cold or cold to warm control each temperature accurately. Many implementations of the process, especially with respect to the first membrane, will involve running the heat exchanger as warm as possible while obtaining exactly the level of enrichment targeted (the lower the temperature, the better purity of product). In turn this would allow maintaining a constant composition of the product even if, for instance, the composition of the feed is changing.
(18) The mixture containing, for example, at least methane and nitrogen, is often supplied to the system at a temperature above 0° C. In many cases, the temperature of the feed stream is initially at or above room temperature. To enhance a separation such as that between N.sub.2 and CH.sub.4, the stream directed to the first stage is cooled in the main heat exchanger to a temperature below 0° C.
(19) A first membrane stage is used to obtain a first permeate, also referred to as a “first permeate stream” (enriched in methane) and a first residue, also referred to as a “first residue stream” (enriched in nitrogen). At least a portion of fluids derived from the first permeate and/or at least a portion of fluids derived from the first residue are heated in the main heat exchanger. As used herein, the terms “fluids derived from the first permeate” and “fluids derived from the first residue” refer to or include any fluid that is obtained, directly or indirectly, after splitting or after treatment steps, from the permeate/residue, such as, for example: 1) a fraction of the initial fluid; 2) the initial fluid or a fraction thereof after a change in conditions (pressure, temperature, vapor fraction); 3) the result of a phase separation after a phase change (for instance if the stream is partially condensed and only the gas or a part of the gas is used); 4) the result of a membrane separation (for instance only the residue or a part of the residue of a membrane treated the initial fluid).
(20) In many cases, the fluids derived from the first permeate that are heated in the main heat exchanger represent a major portion (i.e., more than 50% by mass, such as, for example, at least 80%, at least 85%, at least 90%, at least 95%, at least 98% or even 100% by mass) of the fluids derived from the first permeate. Similarly, the portion of fluids derived from the first residue that are heated in the main heat exchanger represent a major portion (i.e., more than 50% by mass, such as, for example, at least 80%, at least 85%, at least 90%, at least 95%, at least 98% or even 100% by mass) of the fluids derived from the first residue.
(21) According to many aspects of the invention, cooling in the main heat exchanger is provided only by fluids derived from the permeate and/or residue (stream(s)) obtained from the first membrane. In other words, the cooling in the main heat exchanger uses no external fluids, i.e., no fluids other than those derived from the permeate and/or residue generated in the first membrane.
(22) For many embodiments, the main heat exchanger is used to perform all the heating and cooling operations associated with the multi-stage membrane separations conducted in the process and/or system described herein.
(23) In a typical multi-stage separation, the gas mixture containing, for example, at least methane and nitrogen, enters the system in a compressed state (e.g., 50 to 2000 pounds per square inch gauge (psig)). Streams that emerge from a membrane stage can have a reduced pressure and can be compressed using a compressor or another suitable device. In some embodiments, streams such as recyclable and/or product streams are introduced to the compressor at a sub-ambient temperature, to enhance the efficiency of the compression, for example.
(24) Various approaches can be employed to remove nitrogen from a mixture containing at least methane and nitrogen.
(25) Shown in
(26) The two streams obtained from membrane stage 101, i.e., residue stream 3 and permeate stream 4, are directed, respectively, to a second membrane stage 102 (e.g., typically a silicone based rubbery membrane) and a third membrane stage 103 (typically a silicone based rubbery membrane, for example). In many instances, permeate stream 4 is compressed prior to its delivery to third membrane stage 103.
(27) In the process diagram of
(28) In more detail, the product (sales gas) is the methane-rich permeate stream. It exits membrane 103 as stream 6 (at a temperature within the range of from about −5° C. to about −105° C., for example), and is further heated in heat exchanger 100 (e.g., to a temperature within the range of from about 30° C. to about −70° C.), to yield stream 11.
(29) Residue (or retentate) stream 5 from third membrane 103, (having, for instance, a temperature within the range of from about 25° C. to about −75° C.) can be heated in multi-fluid heat exchanger 100 to a temperature within the range of from about 60° C. to about −70° C. The resulting heated fluid stream 12 can be recompressed and recycled back to the first membrane 101. A similar arrangement for recycling back to the first membrane stage 101 can be implemented with respect to the permeate stream 7, exiting second membrane stage 102 (e.g., at a temperature within the range of from about 25° C. to about −75° C.) and heated in the main heat exchanger 100 to form heated stream 10 (characterized, for example, by a temperature within the range of from about 60° C. to about −70° C.).
(30) Stream 8, the residue stream from second membrane stage 102, exits the membrane at a temperature within the range of from about 25° C. to about −75° C.) and is heated in heat exchanger 100 to a temperature within the range of from about 60° C. to about −70° C. to obtain residue stream 9. This stream is the nitrogen-rich, methane-lean component. Although in many cases, this stream is handled as a waste stream, specific embodiments of the invention use the nitrogen-rich component in other application, as further discussed below.
(31) A bypass valve (not shown in
(32) Since the process in membrane 101 can be associated with a large or very large Joule-Thomson effect, residue and permeate can exit this membrane at a very low temperature. In some embodiments, streams 3 and/or 4 are heated to a desired temperature. On the process diagram of
(33) Controls that can be incorporated in the process and/or system of
(34) The efficient operation of the process illustrated in
(35) Another approach applicable in some situations involves a simplified two-stage membrane separation process and/or system. As with other arrangements described herein, this simplified approach can provide a pipeline quality gas stream with an N.sub.2 content of less than 3-5% (by volume) from feed compositions that have a N.sub.2 content of less than 10-15%.
(36) An illustration of a two-stage separation is provided in
(37) Residue stream 53, generated in first membrane stage 201, is directed to second membrane 202 (e.g., a silicone membrane or another suitable rubbery membrane, for example) to produce permeate stream 57 and residue stream 58. These streams can be passed through multi-fluid heat exchanger 100 to produce permeate stream 60, which can be recycled back to the feed, typically after recompression, and the N.sub.2-rich, methane-lean residue stream 59 (a stream that can be handled as a waste product, or used as further described below).
(38) In one illustration, stream 57 has a temperature within the range of from about −5° C. to about −105° C., while stream 60 has a temperature within the range of from about 60° C. to about −75° C. In another illustration, stream 58 has a temperature within the range of from about −5° C. to about −105° C., while stream 59 has a temperature within the range of from about 60° C. to about −75° C. In one implementation an additional control is added for the Joule-Thomson expansion of the second membrane 202 residue stream 58 across a valve.
(39) Residue stream 53 exiting first membrane stage 201 can have a very low temperature (within the range of from about −5° C. to about −105° C., for instance) due to a large or very large Joule-Thomson effect in the first membrane. Many implementations provide for an additional control in which this stream is heated to an appropriate temperature (e.g., from about 25° C. to about −75° C.). In
(40) Permeate stream 54 exits membrane stage 201 at a temperature within the range of from about −5° C. and about −105° C. and is heated in multi-fluid heat exchanger 100 to produce product (sales gas) stream 61, which can have a temperature within the range of from about 60° C. to about −75° C.
(41) As in the approach of
(42) Another multi-stage membrane separation approach uses three-stages and is described with reference to
(43) In many implementations, the initial feed can have a temperature within the range of from about 0° C. to about 80° C. and a pressure within the range of from about 50 psig to about 2000 psig. As shown in
(44) Due to the large and often very large Joule-Thomson effect in membrane 301A, residue and permeate exit this membrane at a low or very low temperature, generally a temperature well below that of fluid stream 406.
(45) In many implementations, residue stream 408 can be reheated before flowing to membrane stage 301B. Raising the temperature of this fluid stream can be performed while valorizing fully the refrigeration available, typically by introducing streams in the same multi-fluid heat exchanger 100, or with additional economizer/heat exchangers. In one example, residue fluid stream 408 exits membrane stage 301A at a temperature within the range of from about −5° C. to about −105° C., e.g., −43° C. This stream is heated in the multi-fluid exchanger 100, to produce stream 417, at a temperature typically above 0° C., for example, (typically within a range of from about −75° C. to about 25° C. Stream 417 is then directed to membrane 301B.
(46) Permeate 418, generated in membrane stage 301B, is heated in multi-fluid heat exchanger 100 from which it exits as fluid stream 409. This fluid is compressed in compressor C1. Providing stream 409 at a sub-ambient temperature (e.g., below 15° C., within the range of from about −80° C. to about 10° C., for example) can improve the efficiency of the compression operation. The compressed stream 435 (characterized by an illustrative temperature within a range of from about −20° C. to about 150° C.), is directed from compressor C1 to multi-fluid heat exchanger 100, before being introduced as stream 411 (having, for instance, a temperature within a range of from about −75° C. to about 25° C., e.g., about 10° C.) to membrane stage 302.
(47) Some of the streams (e.g., permeate 414, from membrane stage 302 and permeate 407, from membrane stage 301A) are heated back up in the multi-fluid heat exchanger 100.
(48) Specifically, permeate stream obtained from membrane stage 301A, namely stream 407, is heated to generate stream 421 which is compressed in compressor C3. Stream 421 can have a temperature within the range of from about −75° C. to about 60 C. Providing stream 421 at a sub-ambient temperature (below 15° C., for instance) can improve the efficiency of the compression. Compressed stream 422, exiting compressor C3 at a temperature (downstream of compressor after-cooler as represented in the figure) within the range of from about 10° C. to about 100° C., is the methane-rich, product (sales gas).
(49) Permeate stream 414, from membrane stage 302, is heated in multi-fluid heat exchanger 100 to form stream 415 which is compressed in compressor C2. The resulting stream 416 is recycled back to the feed. In one example, fluid stream 415 has a sub-ambient temperature, e.g., within the range of from about −75° C. to about 15° C. Compressed fluid stream 416, having, for instance, downstream of after-cooler, a temperature within the range of from about 10° C. to about 100° C., e.g., 49° C., is recycled to the feed mixture to form stream 402.
(50) Residue stream 412 from membrane stage 302 is a nitrogen-rich, methane-lean stream. In some embodiments this residue fraction from membrane 302, namely stream 412, is combined with residue fraction 419, from membrane 301B, to form the nitrogen-rich stream 420. Nitrogen-rich components can be disposed of as waste or can find applications in another operation or elsewhere in the facility. In many embodiments, fluid streams 412 and 419 have temperatures well below 0° C. (e.g., within the range of from about −105° C. to about −5° C.). Either or both streams can be heated (for instance in the main heat exchanger in order to recover additional refrigeration). In the alternative or in addition, it is possible to first combine these streams and then raise the temperature of stream 420 (for instance in the main heat exchanger in order to recover additional refrigeration).
(51) Further operations or controls can be included. For example, stream 403 can be partially heated in multi-fluid heat exchanger 100.
(52)
(53) Stream 422 is the methane-rich product fraction. Residue streams 412 and 419, from membranes 302 and 301B, respectively, are nitrogen-rich fractions. As discussed with reference to
(54) Typically, the nitrogen-rich fraction (e.g., stream 420 in
(55) Operations at low temperature can require a deep removal of moisture, e.g., down to less than 10 ppm, or a dew point of at least 10° C. colder than the membrane operating temperature. Thus, specific embodiments described herein include a drying step that is complementary to the membrane process. In many cases, moisture is removed using adsorption-type dryers, and, in particular, adsorption-type dryers capable of removing moisture to the low levels noted above.
(56) Some embodiments of the invention utilize a multi-bed arrangement (i.e., an arrangement including at least two beds) that can be operated in a continuous fashion, with one adsorption bed in production mode and another in regeneration mode. Adsorption technology based on multi-bed arrangements (pressure swing adsorption or temperature swing adsorption, for instance) are well known in the art. See, e.g., EP0862937B1 as one of many examples of TSA to remove moisture.
(57) In some arrangements, the process and system described herein incorporate adsorption techniques in which the regenerating bed can be purged with the N.sub.2-rich residue gas (see, e.g., steam 9 in
(58) Adsorbent materials that can be employed include but are not limited to silica gel, molecular sieves (e.g., 3A, 4A) and others.
(59) Embodiments described herein can be practiced or adapted to separations other than those involving CH.sub.4—N.sub.2. Illustrative mixtures that could be separated by applying principles discussed above include but are not limited to _Ethane/Methane separation (or more generally NGL separation from natural gas) and CH4/CO separation.
(60) The invention is further illustrated through the following nonlimiting example.
EXAMPLE
(61) A computer simulation was conducted for a system such as that in
(62) TABLE-US-00001 TABLE 1 Component Amount A Mole Frac (Methane) 91.05% B Mole Frac (Ethane) 2.51% C Mole Frac (Propane) 0.16% D Mole Frac (i-Butane) 0.00% E Mole Frac (n-Butane) 0.01% F Mole Frac (i-Pentane) 0.00% G Mole Frac (n-Pentane) 0.00% H Mole Frac (n-Hexane) 0.00% I Mole Frac (n-Heptane) 0.07% J Mole Frac (Nitrogen) 6.20% K Mole Frac (CO2) 0.00% L Mole Frac (n-Octane) 0.00% M Mole Frac (n-Nonane) 0.00% N Mole Frac (H2S) 0.00% O Mole Frac (H2O) 0.00%
(63) Initial conditions of the feed are shown in Table 2.
(64) TABLE-US-00002 TABLE 2 1 Vapour Fraction 1.00 2 Temperature [F.] 120 3 Pressure [psig] 1,000 4 Molar Flow [MMSCFD] 25.00 5 Mass Flow [lb/hr] 47,231 6 HC Dew Point [F.] <empty> 7 H2O Dew Point [F.] <empty> 8 HHV [Btu/SCF] 961
(65) The compositions with respect to components A through O (from Table 1) present in each stream (location) identified in
(66) TABLE-US-00003 TABLE 3A 402 403 404 405 406 407 408 409 410 1 1.00 1.00 1.00 1.00 1.00 1.00 1.00 1.00 1.00 2 120 120 120 −10 8 −50 −45 86 120 3 1,000 1,000 1,000 996 996 25 1,000 146 1,005 4 29.91 4.49 25.42 25.42 29.91 21.65 8.26 5.40 5.40 5 56,230 8,434 47,795 47,795 56,230 40,067 16,163 10,095 10,095 6 <empty> <empty> <empty> <empty> <empty> −166 <empty> −188 <empty> 7 <empty> <empty> <empty> <empty> <empty> <empty> <empty> <empty> <empty> 8 959 959 959 959 959 999 855 924 924 A 91.61% 91.61% 91.61% 91.61% 91.61% 94.07% 85.16% 91.92% 91.92% B 2.12% 2.12% 2.12% 2.12% 2.12% 2.90% 0.09% 0.13% 0.13% C 0.13% 0.13% 0.13% 0.13% 0.13% 0.18% 0.00% 0.00% 0.00% D 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% E 0.00% 0.00% 0.00% 0.00% 0.00% 0.01% 0.00% 0.00% 0.00% F 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% G 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% H 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% I 0.06% 0.06% 0.06% 0.06% 0.06% 0.08% 0.01% 0.01% 0.01% J 6.06% 6.06% 6.06% 6.06% 6.06% 2.76% 14.74% 7.94% 7.94% K 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% L 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% M 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% N 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% O 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00%
(67) TABLE-US-00004 TABLE 3B 410 411 412 414 415 416 417 418 1 1.00 1.00 1.00 1.00 1.00 1.00 1.00 1.00 2 120 50 0 0 86 120 50 30 3 1,005 1,001 1,001 150 146 1,000 996 150 4 5.40 5.40 0.50 4.91 4.91 4.91 8.26 5.40 5 10,095 10,095 1,096 8,999 8,999 8,999 16,163 10,095 6 <empty> <empty> <empty> −186 −187 <empty> <empty> −187 7 <empty> <empty> <empty> <empty> <empty> <empty> <empty> <empty> 8 924 924 667 950 950 950 855 924 A 91.92% 91.92% 66.56% 94.50% 94.50% 94.49% 85.16% 91.92% B 0.13% 0.13% 0.00% 0.14% 0.14% 0.14% 0.09% 0.13% C 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% D 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% E 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% F 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% G 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% H 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% I 0.01% 0.01% 0.00% 0.01% 0.01% 0.01% 0.01% 0.01% J 7.94% 7.94% 33.43% 5.35% 5.35% 5.35% 14.74% 7.94% K 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% L 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% M 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% N 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% O 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00% 0.00%
(68) TABLE-US-00005 TABLE 3C 419 420 421 422 1 1.00 1.00 1.00 1.00 2 −5 −4 86 120 3 991 991 21 770 4 2.86 3.35 21.65 21.65 5 6,068 7,164 40,067 40,067 6 <empty> <empty> −168 <empty> 7 <empty> <empty> <empty> <empty> 8 726 717 999 999 A 72.37% 71.51% 94.07% 94.07% B 0.02% 0.01% 2.90% 2.90% B 0.00% 0.00% 0.18% 0.18% D 0.00% 0.00% 0.00% 0.00% E 0.00% 0.00% 0.01% 0.01% F 0.00% 0.00% 0.00% 0.00% G 0.00% 0.00% 0.00% 0.00% H 0.00% 0.00% 0.00% 0.00% I 0.00% 0.00% 0.08% 0.08% J 27.61% 28.47% 2.76% 2.76% K 0.00% 0.00% 0.00% 0.00% L 0.00% 0.00% 0.00% 0.00% M 0.00% 0.00% 0.00% 0.00% N 0.00% 0.00% 0.00% 0.00% O 0.00% 0.00% 0.00% 0.00%
(69) As seen in the results of the computer simulation, it is possible to obtain efficiently a methane product containing less than 3% mol of nitrogen while recovering more than 90% of the hydrocarbons thanks to this process.
(70) While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims.