CA2764590C - Hydrocarbon gas processing - Google Patents
Hydrocarbon gas processing Download PDFInfo
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- CA2764590C CA2764590C CA2764590A CA2764590A CA2764590C CA 2764590 C CA2764590 C CA 2764590C CA 2764590 A CA2764590 A CA 2764590A CA 2764590 A CA2764590 A CA 2764590A CA 2764590 C CA2764590 C CA 2764590C
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- 238000012545 processing Methods 0.000 title claims abstract description 66
- 229930195733 hydrocarbon Natural products 0.000 title claims abstract description 30
- 150000002430 hydrocarbons Chemical class 0.000 title claims abstract description 30
- 239000004215 Carbon black (E152) Substances 0.000 title claims abstract description 23
- 239000007788 liquid Substances 0.000 claims abstract description 136
- 238000012546 transfer Methods 0.000 claims abstract description 90
- 238000004821 distillation Methods 0.000 claims abstract description 64
- 238000000034 method Methods 0.000 claims abstract description 57
- 230000008569 process Effects 0.000 claims abstract description 57
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 56
- 238000001816 cooling Methods 0.000 claims description 38
- 238000010438 heat treatment Methods 0.000 claims description 29
- 238000005057 refrigeration Methods 0.000 claims description 21
- 239000013589 supplement Substances 0.000 claims description 9
- 238000000926 separation method Methods 0.000 claims description 5
- 238000007599 discharging Methods 0.000 claims 2
- 239000007789 gas Substances 0.000 description 57
- 238000011084 recovery Methods 0.000 description 20
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 18
- 238000005194 fractionation Methods 0.000 description 14
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 11
- 239000003345 natural gas Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 239000001294 propane Substances 0.000 description 9
- 239000012263 liquid product Substances 0.000 description 8
- 230000000630 rising effect Effects 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- 238000009833 condensation Methods 0.000 description 7
- 230000005494 condensation Effects 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- 238000010586 diagram Methods 0.000 description 5
- 230000000153 supplemental effect Effects 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 238000005265 energy consumption Methods 0.000 description 4
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical class CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 4
- 238000012856 packing Methods 0.000 description 4
- 239000012855 volatile organic compound Substances 0.000 description 4
- 235000013844 butane Nutrition 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- -1 naphtha Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000003507 refrigerant Substances 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical class CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- QUJJSTFZCWUUQG-UHFFFAOYSA-N butane ethane methane propane Chemical class C.CC.CCC.CCCC QUJJSTFZCWUUQG-UHFFFAOYSA-N 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 239000005431 greenhouse gas Substances 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000004088 simulation Methods 0.000 description 2
- 150000003464 sulfur compounds Chemical class 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 235000013847 iso-butane Nutrition 0.000 description 1
- 239000003077 lignite Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 239000004058 oil shale Substances 0.000 description 1
- 238000011027 product recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
- F25J3/02—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
- F25J3/0204—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the feed stream
- F25J3/0209—Natural gas or substitute natural gas
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G5/00—Recovery of liquid hydrocarbon mixtures from gases, e.g. natural gas
- C10G5/04—Recovery of liquid hydrocarbon mixtures from gases, e.g. natural gas with liquid absorbents
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G5/00—Recovery of liquid hydrocarbon mixtures from gases, e.g. natural gas
- C10G5/06—Recovery of liquid hydrocarbon mixtures from gases, e.g. natural gas by cooling or compressing
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
- F25J3/02—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
- F25J3/0228—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream
- F25J3/0233—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of CnHm with 1 carbon atom or more
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
- F25J3/02—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
- F25J3/0228—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream
- F25J3/0242—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of CnHm with 3 carbon atoms or more
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1025—Natural gas
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2200/00—Processes or apparatus using separation by rectification
- F25J2200/02—Processes or apparatus using separation by rectification in a single pressure main column system
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2200/00—Processes or apparatus using separation by rectification
- F25J2200/30—Processes or apparatus using separation by rectification using a side column in a single pressure column system
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2200/00—Processes or apparatus using separation by rectification
- F25J2200/74—Refluxing the column with at least a part of the partially condensed overhead gas
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2200/00—Processes or apparatus using separation by rectification
- F25J2200/78—Refluxing the column with a liquid stream originating from an upstream or downstream fractionator column
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2205/00—Processes or apparatus using other separation and/or other processing means
- F25J2205/02—Processes or apparatus using other separation and/or other processing means using simple phase separation in a vessel or drum
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2205/00—Processes or apparatus using other separation and/or other processing means
- F25J2205/02—Processes or apparatus using other separation and/or other processing means using simple phase separation in a vessel or drum
- F25J2205/04—Processes or apparatus using other separation and/or other processing means using simple phase separation in a vessel or drum in the feed line, i.e. upstream of the fractionation step
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2235/00—Processes or apparatus involving steps for increasing the pressure or for conveying of liquid process streams
- F25J2235/60—Processes or apparatus involving steps for increasing the pressure or for conveying of liquid process streams the fluid being (a mixture of) hydrocarbons
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2240/00—Processes or apparatus involving steps for expanding of process streams
- F25J2240/02—Expansion of a process fluid in a work-extracting turbine (i.e. isentropic expansion), e.g. of the feed stream
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2270/00—Refrigeration techniques used
- F25J2270/12—External refrigeration with liquid vaporising loop
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2270/00—Refrigeration techniques used
- F25J2270/60—Closed external refrigeration cycle with single component refrigerant [SCR], e.g. C1-, C2- or C3-hydrocarbons
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2290/00—Other details not covered by groups F25J2200/00 - F25J2280/00
- F25J2290/40—Vertical layout or arrangement of cold equipments within in the cold box, e.g. columns, condensers, heat exchangers etc.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- Mechanical Engineering (AREA)
- Thermal Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Separation By Low-Temperature Treatments (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A process and an apparatus are disclosed for a compact processing assembly to recover C2 (or C3) components and heavier hydrocarbon components from a hydrocarbon gas stream. The gas stream is cooled and divided into first and second streams. The first stream is further cooled, expanded to lower pressure, and supplied as a feed between first and second absorbing means. The second stream is expanded to lower pressure and supplied as bottom feed to the second absorbing means. A distilla-tion vapor stream from the first absorbing means is heated, compressed to higher pressure, and divided into a volatile residue gas fraction and a compressed recycle stream. The compressed recycle stream is cooled, expanded to lower pressure, and supplied as top feed to the first absorbing means. A distillation liquid stream from the second absorbing means is heated in a heat and mass transfer means to strip out its volatile components.
Description
HYDROCARBON GAS PROCESSING
SPECIFICATION
BACKGROUND OF THE INVENTION
[0001] Ethylene, ethane, propylene, propane, and/or heavier hydrocarbons can be recovered from a variety of gases, such as natural gas, refinery gas, and synthetic gas streams obtained from other hydrocarbon materials such as coal, crude oil, naphtha, oil shale, tar sands, and lignite. Natural gas usually has a major proportion of methane and ethane, i.e., methane and ethane together comprise at least 50 mole percent of the gas. The gas also contains relatively lesser amounts of heavier hydrocarbons such as propane, butanes, pentanes, and the like, as well as hydrogen, nitrogen, carbon dioxide, and other gases.
SPECIFICATION
BACKGROUND OF THE INVENTION
[0001] Ethylene, ethane, propylene, propane, and/or heavier hydrocarbons can be recovered from a variety of gases, such as natural gas, refinery gas, and synthetic gas streams obtained from other hydrocarbon materials such as coal, crude oil, naphtha, oil shale, tar sands, and lignite. Natural gas usually has a major proportion of methane and ethane, i.e., methane and ethane together comprise at least 50 mole percent of the gas. The gas also contains relatively lesser amounts of heavier hydrocarbons such as propane, butanes, pentanes, and the like, as well as hydrogen, nitrogen, carbon dioxide, and other gases.
[0002] The present invention is generally concerned with the recovery of ethylene, ethane, propylene, propane, and heavier hydrocarbons from such gas streams. A typical analysis of a gas stream to be processed in accordance with this invention would be, in approximate mole percent, 90.3% methane, 4.0% ethane and other C2 components, 1.7% propane and other C3 components, 0.3% iso-butane, 0.5%
normal butane, and 0.8% pentanes plus, with the balance made up of nitrogen and carbon dioxide. Sulfur containing gases are also sometimes present.
normal butane, and 0.8% pentanes plus, with the balance made up of nitrogen and carbon dioxide. Sulfur containing gases are also sometimes present.
[0003] The historically cyclic fluctuations in the prices of both natural gas and its natural gas liquid (NGL) constituents have at times reduced the incremental value of ethane, ethylene, propane, propylene, and heavier components as liquid products.
This has resulted in a demand for processes that can provide more efficient recoveries of these products and for processes that can provide efficient recoveries with lower capital investment. Available processes for separating these materials include those based upon cooling and refrigeration of gas, oil absorption, and refrigerated oil absorption. Additionally, cryogenic processes have become popular because of the availability of economical equipment that produces power while simultaneously expanding and extracting heat from the gas being processed. Depending upon the pressure of the gas source, the richness (ethane, ethylene, and heavier hydrocarbons content) of the gas, and the desired end products, each of these processes or a combination thereof may be employed.
This has resulted in a demand for processes that can provide more efficient recoveries of these products and for processes that can provide efficient recoveries with lower capital investment. Available processes for separating these materials include those based upon cooling and refrigeration of gas, oil absorption, and refrigerated oil absorption. Additionally, cryogenic processes have become popular because of the availability of economical equipment that produces power while simultaneously expanding and extracting heat from the gas being processed. Depending upon the pressure of the gas source, the richness (ethane, ethylene, and heavier hydrocarbons content) of the gas, and the desired end products, each of these processes or a combination thereof may be employed.
[0004] The cryogenic expansion process is now generally preferred for natural gas liquids recovery because it provides maximum simplicity with ease of startup, operating flexibility, good efficiency, safety, and good reliability. U.S.
Patent Nos.
3,292,380; 4,061,481; 4,140,504; 4,157,904; 4,171,964; 4,185,978; 4,251,249;
4,278,457; 4,519,824; 4,617,039; 4,687,499; 4,689,063; 4,690,702; 4,854,955;
4,869,740; 4,889,545; 5,275,005; 5,555,748; 5,566,554; 5,568,737; 5,771,712;
Patent Nos.
3,292,380; 4,061,481; 4,140,504; 4,157,904; 4,171,964; 4,185,978; 4,251,249;
4,278,457; 4,519,824; 4,617,039; 4,687,499; 4,689,063; 4,690,702; 4,854,955;
4,869,740; 4,889,545; 5,275,005; 5,555,748; 5,566,554; 5,568,737; 5,771,712;
5,799,507; 5,881,569; 5,890,378; 5,983,664; 6,182,469; 6,578,379; 6,712,880;
6 6,915,662; 7,191,617; 7,219,513; reissue U.S. Patent No. 33,408; and co-pending application nos. 11/430,412; 11/839,693; 11/971,491; 12/206,230; 12/689,616;
12/717,394; 12/750,862; 12/772,472; 12/781,259; 12/868,993; 12/869,007;
12/869,139; 12/979,563; 13/048,315; and 13/051,682 describe relevant processes (although the description of the present invention in some cases is based on different processing conditions than those described in the cited U.S. Patents).
[0005] In a typical cryogenic expansion recovery process, a feed gas stream under pressure is cooled by heat exchange with other streams of the process and/or external sources of refrigeration such as a propane compression-refrigeration system.
As the gas is cooled, liquids may be condensed and collected in one or more separators as high-pressure liquids containing some of the desired C2+
components.
Depending on the richness of the gas and the amount of liquids formed, the high-pressure liquids may be expanded to a lower pressure and fractionated.
The vaporization occurring during expansion of the liquids results in further cooling of the stream. Under some conditions, pre-cooling the high pressure liquids prior to the expansion may be desirable in order to further lower the temperature resulting from the expansion. The expanded stream, comprising a mixture of liquid and vapor, is fractionated in a distillation (demethanizer or deethanizer) column. In the column, the expansion cooled stream(s) is (are) distilled to separate residual methane, nitrogen, and other volatile gases as overhead vapor from the desired C2 components, C3 components, and heavier hydrocarbon components as bottom liquid product, or to separate residual methane, C2 components, nitrogen, and other volatile gases as overhead vapor from the desired C3 components and heavier hydrocarbon components as bottom liquid product.
[0006] If the feed gas is not totally condensed (typically it is not), the vapor remaining from the partial condensation can be split into two streams. One portion of the vapor is passed through a work expansion machine or engine, or an expansion valve, to a lower pressure at which additional liquids are condensed as a result of further cooling of the stream. The pressure after expansion is essentially the same as the pressure at which the distillation column is operated. The combined vapor-liquid phases resulting from the expansion are supplied as feed to the column.
12/717,394; 12/750,862; 12/772,472; 12/781,259; 12/868,993; 12/869,007;
12/869,139; 12/979,563; 13/048,315; and 13/051,682 describe relevant processes (although the description of the present invention in some cases is based on different processing conditions than those described in the cited U.S. Patents).
[0005] In a typical cryogenic expansion recovery process, a feed gas stream under pressure is cooled by heat exchange with other streams of the process and/or external sources of refrigeration such as a propane compression-refrigeration system.
As the gas is cooled, liquids may be condensed and collected in one or more separators as high-pressure liquids containing some of the desired C2+
components.
Depending on the richness of the gas and the amount of liquids formed, the high-pressure liquids may be expanded to a lower pressure and fractionated.
The vaporization occurring during expansion of the liquids results in further cooling of the stream. Under some conditions, pre-cooling the high pressure liquids prior to the expansion may be desirable in order to further lower the temperature resulting from the expansion. The expanded stream, comprising a mixture of liquid and vapor, is fractionated in a distillation (demethanizer or deethanizer) column. In the column, the expansion cooled stream(s) is (are) distilled to separate residual methane, nitrogen, and other volatile gases as overhead vapor from the desired C2 components, C3 components, and heavier hydrocarbon components as bottom liquid product, or to separate residual methane, C2 components, nitrogen, and other volatile gases as overhead vapor from the desired C3 components and heavier hydrocarbon components as bottom liquid product.
[0006] If the feed gas is not totally condensed (typically it is not), the vapor remaining from the partial condensation can be split into two streams. One portion of the vapor is passed through a work expansion machine or engine, or an expansion valve, to a lower pressure at which additional liquids are condensed as a result of further cooling of the stream. The pressure after expansion is essentially the same as the pressure at which the distillation column is operated. The combined vapor-liquid phases resulting from the expansion are supplied as feed to the column.
[0007] The remaining portion of the vapor is cooled to substantial condensation by heat exchange with other process streams, e.g., the cold fractionation tower overhead. Some or all of the high-pressure liquid may be combined with this vapor portion prior to cooling. The resulting cooled stream is then expanded through an appropriate expansion device, such as an expansion valve, to the pressure at which the demethanizer is operated. During expansion, a portion of the liquid will vaporize, resulting in cooling of the total stream. The flash expanded stream is then supplied as top feed to the demethanizer. Typically, the vapor portion of the flash expanded stream and the demethanizer overhead vapor combine in an upper separator section in the fractionation tower as residual methane product gas. Alternatively, the cooled and expanded stream may be supplied to a separator to provide vapor and liquid streams.
The vapor is combined with the tower overhead and the liquid is supplied to the column as a top column feed.
The vapor is combined with the tower overhead and the liquid is supplied to the column as a top column feed.
[0008] In the ideal operation of such a separation process, the residue gas leaving the process will contain substantially all of the methane in the feed gas with essentially none of the heavier hydrocarbon components and the bottoms fraction leaving the demethanizer will contain substantially all of the heavier hydrocarbon components with essentially no methane or more volatile components. In practice, however, this ideal situation is not obtained because the conventional demethanizer is operated largely as a stripping column. The methane product of the process, therefore, typically comprises vapors leaving the top fractionation stage of the column, together with vapors not subjected to any rectification step.
Considerable losses of C2, C3, and C4+ components occur because the top liquid feed contains substantial quantities of these components and heavier hydrocarbon components, resulting in corresponding equilibrium quantities of C2 components, C3 components, C4 components, and heavier hydrocarbon components in the vapors leaving the top fractionation stage of the demethanizer. The loss of these desirable components could be significantly reduced if the rising vapors could be brought into contact with a significant quantity of liquid (reflux) capable of absorbing the C2 components, C3 components, C4 components, and heavier hydrocarbon components from the vapors.
Considerable losses of C2, C3, and C4+ components occur because the top liquid feed contains substantial quantities of these components and heavier hydrocarbon components, resulting in corresponding equilibrium quantities of C2 components, C3 components, C4 components, and heavier hydrocarbon components in the vapors leaving the top fractionation stage of the demethanizer. The loss of these desirable components could be significantly reduced if the rising vapors could be brought into contact with a significant quantity of liquid (reflux) capable of absorbing the C2 components, C3 components, C4 components, and heavier hydrocarbon components from the vapors.
[0009] In recent years, the preferred processes for hydrocarbon separation use an upper absorber section to provide additional rectification of the rising vapors. The source of the reflux stream for the upper rectification section is typically a recycled stream of residue gas supplied under pressure. The recycled residue gas stream is usually cooled to substantial condensation by heat exchange with other process streams, e.g., the cold fractionation tower overhead. The resulting substantially condensed stream is then expanded through an appropriate expansion device, such as an expansion valve, to the pressure at which the demethanizer is operated.
During expansion, a portion of the liquid will usually vaporize, resulting in cooling of the total stream. The flash expanded stream is then supplied as top feed to the demethanizer. Typically, the vapor portion of the expanded stream and the demethanizer overhead vapor combine in an upper separator section in the fractionation tower as residual methane product gas. Alternatively, the cooled and expanded stream may be supplied to a separator to provide vapor and liquid streams, so that thereafter the vapor is combined with the tower overhead and the liquid is supplied to the column as a top column feed. Typical process schemes of this type are disclosed in U.S. Patent Nos. 4,889,545; 5,568,737; and 5,881,569, co-pending application nos. 11/430,412; 11/971,491; and 12/717,394, and in Mowrey, E.
Ross, "Efficient, High Recovery of Liquids from Natural Gas Utilizing a High Pressure Absorber", Proceedings of the Eighty-First Annual Convention of the Gas Processors Association, Dallas, Texas, March 11-13, 2002.
During expansion, a portion of the liquid will usually vaporize, resulting in cooling of the total stream. The flash expanded stream is then supplied as top feed to the demethanizer. Typically, the vapor portion of the expanded stream and the demethanizer overhead vapor combine in an upper separator section in the fractionation tower as residual methane product gas. Alternatively, the cooled and expanded stream may be supplied to a separator to provide vapor and liquid streams, so that thereafter the vapor is combined with the tower overhead and the liquid is supplied to the column as a top column feed. Typical process schemes of this type are disclosed in U.S. Patent Nos. 4,889,545; 5,568,737; and 5,881,569, co-pending application nos. 11/430,412; 11/971,491; and 12/717,394, and in Mowrey, E.
Ross, "Efficient, High Recovery of Liquids from Natural Gas Utilizing a High Pressure Absorber", Proceedings of the Eighty-First Annual Convention of the Gas Processors Association, Dallas, Texas, March 11-13, 2002.
[0010] The present invention employs a novel means of perfoiming the various steps described above more efficiently and using fewer pieces of equipment.
This is accomplished by combining what heretofore have been individual equipment items into a common housing, thereby reducing the plot space required for the processing plant and reducing the capital cost of the facility. Surprisingly, applicants have found that the more compact arrangement also significantly reduces the power consumption required to achieve a given recovery level, thereby increasing the process efficiency and reducing the operating cost of the facility. In addition, the more compact arrangement also eliminates much of the piping used to interconnect the individual equipment items in traditional plant designs, further reducing capital cost and also eliminating the associated flanged piping connections. Since piping flanges are a potential leak source for hydrocarbons (which are volatile organic compounds, VOCs, that contribute to greenhouse gases and may also be precursors to atmospheric ozone foimation), eliminating these flanges reduces the potential for atmospheric emissions that can damage the environment.
This is accomplished by combining what heretofore have been individual equipment items into a common housing, thereby reducing the plot space required for the processing plant and reducing the capital cost of the facility. Surprisingly, applicants have found that the more compact arrangement also significantly reduces the power consumption required to achieve a given recovery level, thereby increasing the process efficiency and reducing the operating cost of the facility. In addition, the more compact arrangement also eliminates much of the piping used to interconnect the individual equipment items in traditional plant designs, further reducing capital cost and also eliminating the associated flanged piping connections. Since piping flanges are a potential leak source for hydrocarbons (which are volatile organic compounds, VOCs, that contribute to greenhouse gases and may also be precursors to atmospheric ozone foimation), eliminating these flanges reduces the potential for atmospheric emissions that can damage the environment.
[0011] In accordance with the present invention, it has been found that C2 recoveries in excess of 95% can be obtained. Similarly, in those instances where recovery of C2 components is not desired, C3 recoveries in excess of 95% can be maintained. In addition, the present invention makes possible essentially 100%
separation of methane (or C2 components) and lighter components from the C2 components (or C3 components) and heavier components at lower energy requirements compared to the prior art while maintaining the same recovery level.
The present invention, although applicable at lower pressures and warmer temperatures, is particularly advantageous when processing feed gases in the range of 400 to 1500 psia [2,758 to 10,342 kPa(a)] or higher under conditions requiring NGL
recovery column overhead temperatures of -50 F [-46 C] or colder.
separation of methane (or C2 components) and lighter components from the C2 components (or C3 components) and heavier components at lower energy requirements compared to the prior art while maintaining the same recovery level.
The present invention, although applicable at lower pressures and warmer temperatures, is particularly advantageous when processing feed gases in the range of 400 to 1500 psia [2,758 to 10,342 kPa(a)] or higher under conditions requiring NGL
recovery column overhead temperatures of -50 F [-46 C] or colder.
[0012] For a better understanding of the present invention, reference is made to the following examples and drawings. Referring to the drawings:
[0013] FIG. 1 is a flow diagram of a prior art natural gas processing plant in accordance with United States Patent No. 5,568,737;
[0014] FIG. 2 is a flow diagram of a natural gas processing plant in accordance with the present invention; and
[0015] FIGS. 3 through 17 are flow diagrams illustrating alternative means of application of the present invention to a natural gas stream.
[0016] In the following explanation of the above figures, tables are provided summarizing flow rates calculated for representative process conditions. In the tables appearing herein, the values for flow rates (in moles per hour) have been rounded to the nearest whole number for convenience. The total stream rates shown in the tables include all non-hydrocarbon components and hence are generally larger than the sum of the stream flow rates for the hydrocarbon components. Temperatures indicated are approximate values rounded to the nearest degree. It should also be noted that the process design calculations performed for the purpose of comparing the processes depicted in the figures are based on the assumption of no heat leak from (or to) the surroundings to (or from) the process. The quality of commercially available insulating materials makes this a very reasonable assumption and one that is typically made by those skilled in the art.
[0017] For convenience, process parameters are reported in both the traditional British units and in the units of the Systeme International d'Unites (SI).
The molar flow rates given in the tables may be interpreted as either pound moles per hour or kilogram moles per hour. The energy consumptions reported as horsepower (HP) and/or thousand British Thermal Units per hour (MBTU/Hr) correspond to the stated molar flow rates in pound moles per hour. The energy consumptions reported as kilowatts (kW) correspond to the stated molar flow rates in kilogram moles per hour.
DESCRIPTION OF THE PRIOR ART
The molar flow rates given in the tables may be interpreted as either pound moles per hour or kilogram moles per hour. The energy consumptions reported as horsepower (HP) and/or thousand British Thermal Units per hour (MBTU/Hr) correspond to the stated molar flow rates in pound moles per hour. The energy consumptions reported as kilowatts (kW) correspond to the stated molar flow rates in kilogram moles per hour.
DESCRIPTION OF THE PRIOR ART
[0018] FIG. 1 is a process flow diagram showing the design of a processing plant to recover C2+ components from natural gas using prior art according to U.S.
Pat. No. 5,568,737. In this simulation of the process, inlet gas enters the plant at 110 F [43 C] and 915 psia [6,307 kPa(a)] as stream 31. If the inlet gas contains a concentration of sulfur compounds which would prevent the product streams from meeting specifications, the sulfur compounds are removed by appropriate pretreatment of the feed gas (not illustrated). In addition, the feed stream is usually dehydrated to prevent hydrate (ice) formation under cryogenic conditions.
Solid desiccant has typically been used for this purpose.
Pat. No. 5,568,737. In this simulation of the process, inlet gas enters the plant at 110 F [43 C] and 915 psia [6,307 kPa(a)] as stream 31. If the inlet gas contains a concentration of sulfur compounds which would prevent the product streams from meeting specifications, the sulfur compounds are removed by appropriate pretreatment of the feed gas (not illustrated). In addition, the feed stream is usually dehydrated to prevent hydrate (ice) formation under cryogenic conditions.
Solid desiccant has typically been used for this purpose.
[0019] The feed stream 31 is divided into two portions, streams 32 and 33.
Stream 32 is cooled to -26 F [-32 C] in heat exchanger 10 by heat exchange with cool distillation vapor stream 41a, while stream 33 is cooled to -32 F [-35 C] in heat exchanger 11 by heat exchange with demethanizer reboiler liquids at 41 F [5 C]
(stream 43) and side reboiler liquids at -49 F [-45 C] (stream 42). Streams 32a and 33a recombine to form stream 31a, which enters separator 12 at -28 F [-33 C]
and 893 psia [6,155 kPa(a)] where the vapor (stream 34) is separated from the condensed liquid (stream 35).
Stream 32 is cooled to -26 F [-32 C] in heat exchanger 10 by heat exchange with cool distillation vapor stream 41a, while stream 33 is cooled to -32 F [-35 C] in heat exchanger 11 by heat exchange with demethanizer reboiler liquids at 41 F [5 C]
(stream 43) and side reboiler liquids at -49 F [-45 C] (stream 42). Streams 32a and 33a recombine to form stream 31a, which enters separator 12 at -28 F [-33 C]
and 893 psia [6,155 kPa(a)] where the vapor (stream 34) is separated from the condensed liquid (stream 35).
[0020] The vapor (stream 34) from separator 12 is divided into two streams, 36 and 39. Stream 36, containing about 27% of the total vapor, is combined with the separator liquid (stream 35), and the combined stream 38 passes through heat exchanger 13 in heat exchange relation with cold distillation vapor stream 41 where it is cooled to substantial condensation. The resulting substantially condensed stream 38a at -139 F [-95 C] is then flash expanded through expansion valve 14 to the operating pressure (approximately 396 psia [2,730 kPa(a)]) of fractionation tower 18.
During expansion a portion of the stream is vaporized, resulting in cooling of the total stream. In the process illustrated in FIG. 1, the expanded stream 38b leaving expansion valve 14 reaches a temperature of -140 F [-95 C] and is supplied to fractionation tower 18 at a first mid-column feed point.
During expansion a portion of the stream is vaporized, resulting in cooling of the total stream. In the process illustrated in FIG. 1, the expanded stream 38b leaving expansion valve 14 reaches a temperature of -140 F [-95 C] and is supplied to fractionation tower 18 at a first mid-column feed point.
[0021] The remaining 73% of the vapor from separator 12 (stream 39) enters a work expansion machine 15 in which mechanical energy is extracted from this portion of the high pressure feed. The machine 15 expands the vapor substantially isentropically to the tower operating pressure, with the work expansion cooling the expanded stream 39a to a temperature of approximately -95 F [-71 C]. The typical commercially available expanders are capable of recovering on the order of 80-85%
of the work theoretically available in an ideal isentropic expansion. The work recovered is often used to drive a centrifugal compressor (such as item 16) that can be used to re-compress the heated distillation vapor stream (stream 41b), for example.
The partially condensed expanded stream 39a is thereafter supplied as feed to fractionation tower 18 at a second mid-column feed point.
of the work theoretically available in an ideal isentropic expansion. The work recovered is often used to drive a centrifugal compressor (such as item 16) that can be used to re-compress the heated distillation vapor stream (stream 41b), for example.
The partially condensed expanded stream 39a is thereafter supplied as feed to fractionation tower 18 at a second mid-column feed point.
[0022] The recompressed and cooled distillation vapor stream 41e is divided into two streams. One portion, stream 46, is the volatile residue gas product.
The other portion, recycle stream 45, flows to heat exchanger 10 where it is cooled to -26 F [-32 C] by heat exchange with cool distillation vapor stream 41a. The cooled recycle stream 45a then flows to exchanger 13 where it is cooled to -139 F [-95 C]
and substantially condensed by heat exchange with cold distillation vapor stream 41.
The substantially condensed stream 45b is then expanded through an appropriate expansion device, such as expansion valve 22, to the demethanizer operating pressure, resulting in cooling of the total stream to -147 F [-99 C]. The expanded stream 45c is then supplied to fractionation tower 18 as the top column feed. The vapor portion (if any) of stream 45c combines with the vapors rising from the top fractionation stage of the column to form distillation vapor stream 41, which is withdrawn from an upper region of the tower.
The other portion, recycle stream 45, flows to heat exchanger 10 where it is cooled to -26 F [-32 C] by heat exchange with cool distillation vapor stream 41a. The cooled recycle stream 45a then flows to exchanger 13 where it is cooled to -139 F [-95 C]
and substantially condensed by heat exchange with cold distillation vapor stream 41.
The substantially condensed stream 45b is then expanded through an appropriate expansion device, such as expansion valve 22, to the demethanizer operating pressure, resulting in cooling of the total stream to -147 F [-99 C]. The expanded stream 45c is then supplied to fractionation tower 18 as the top column feed. The vapor portion (if any) of stream 45c combines with the vapors rising from the top fractionation stage of the column to form distillation vapor stream 41, which is withdrawn from an upper region of the tower.
[0023] The demethanizer in tower 18 is a conventional distillation column containing a plurality of vertically spaced trays, one or more packed beds, or some combination of trays and packing. As is often the case in natural gas processing plants, the fractionation tower may consist of two sections. The upper section 18a is a separator wherein the partially vaporized top feed is divided into its respective vapor and liquid portions, and wherein the vapor rising from the lower distillation or demethanizing section 18b is combined with the vapor portion of the top feed to form the cold demethanizer overhead vapor (stream 41) which exits the top of the tower at -144 F [-98 C]. The lower, demethanizing section 18b contains the trays and/or packing and provides the necessary contact between the liquids falling downward and the vapors rising upward. The demethanizing section 18b also includes reboilers (such as the reboiler and the side reboiler described previously) which heat and vaporize a portion of the liquids flowing down the column to provide the stripping vapors which flow up the column to strip the liquid product, stream 44, of methane and lighter components.
10024] The liquid product stream 44 exits the bottom of the tower at [18 C], based on a typical specification of a methane to ethane ratio of 0.010:1 on a mass basis in the bottom product. The demethanizer overhead vapor stream 41 passes countercurrently to the incoming feed gas and recycle stream in heat exchanger where it is heated to -40 F [-40 C] (stream 41a) and in heat exchanger 10 where it is heated to 104 F [40 C] (stream 41b). The distillation vapor stream is then re-compressed in two stages. The first stage is compressor 16 driven by expansion machine 15. The second stage is compressor 20 driven by a supplemental power source which compresses the residue gas (stream 41d) to sales line pressure.
After cooling to 110 F [43 C] in discharge cooler 21, stream 41e is split into the residue gas product (stream 46) and the recycle stream 45 as described earlier. Residue gas stream 46 flows to the sales gas pipeline at 915 psia [6,307 kPa(a)], sufficient to meet line requirements (usually on the order of the inlet pressure).
[0025] A summary of stream flow rates and energy consumption for the process illustrated in FIG. 1 is set forth in the following table:
Table I
(FIG. 1) Stream Flow Summary - Lb. Moles/Hr [kg moles/Hr]
Stream Methane Ethane Propane Butanes+
Total 31 12,398 546 233 229 13,726 32 8,431 371 159 156 9,334 33 3,967 175 74 73 4,392 34 12,195 501 179 77 13,261 36 3,317 136 49 21 3,607 38 3,520 181 103 173 4,072 39 8,878 365 130 56 9,654 41 13,765 30 0 0 13,992 45 1,377 3 0 0 1,400 46 12,388 27 0 0 12,592 1,134 Recoveries*
Ethane 94.99%
Propane 99.99%
Butanes+ 100.00%
Power Residue Gas Compression 6,149 HP [
10,109 kW]
* (Based on un-rounded flow rates) DESCRIPTION OF THE INVENTION
[00261 FIG. 2 illustrates a flow diagram of a process in accordance with the present invention. The feed gas composition and conditions considered in the process presented in FIG. 2 are the same as those in FIG. 1. Accordingly, the FIG. 2 process can be compared with that of the FIG. 1 process to illustrate the advantages of the present invention.
[00271 In the simulation of the FIG. 2 process, inlet gas enters the plant as stream 31 and is divided into two portions, streams 32 and 33. The first portion, stream 32, enters a heat exchange means in the upper region of feed cooling section 118a inside processing assembly 118. This heat exchange means may be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers. The heat exchange means is configured to provide heat exchange between stream 32 flowing through one pass of the heat exchange means and a distillation vapor stream arising from separator section 118b inside processing assembly 118 that has been heated in a heat exchange means in the lower region of feed cooling section 118a. Stream 32 is cooled while further heating the distillation vapor stream, with stream 32a leaving the heat exchange means at -[-32 C].
[0028] The second portion, stream 33, enters a heat and mass transfer means in demethanizing section 118e inside processing assembly 118. This heat and mass transfer means may also be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers.
The heat and mass transfer means is configured to provide heat exchange between stream flowing through one pass of the heat and mass transfer means and a distillation liquid stream flowing downward from absorbing section 118d inside processing assembly 118, so that stream 33 is cooled while heating the distillation liquid stream, cooling stream 33a to -47 F [-44 C] before it leaves the heat and mass transfer means.
As the distillation liquid stream is heated, a portion of it is vaporized to form stripping vapors that rise upward as the remaining liquid continues flowing downward through the heat and mass transfer means. The heat and mass transfer means provides continuous contact between the stripping vapors and the distillation liquid stream so that it also functions to provide mass transfer between the vapor and liquid phases, stripping the liquid product stream 44 of methane and lighter components.
[0029] Streams 32a and 33a recombine to form stream 31a, which enters separator section 118f inside processing assembly 118 at -32 F [-36 C] and 900 psia [6,203 kPa(a)], whereupon the vapor (stream 34) is separated from the condensed liquid (stream 35). Separator section 118f has an internal head or other means to divide it from demethanizing section 118e, so that the two sections inside processing assembly 118 can operate at different pressures.
[0030] The vapor (stream 34) from separator section 118f is divided into two streams, 36 and 39. Stream 36, containing about 27% of the total vapor, is combined with the separated liquid (stream 35, via stream 37), and the combined stream enters a heat exchange means in the lower region of feed cooling section 118a inside processing assembly 118. This heat exchange means may likewise be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers. The heat exchange means is configured to provide heat exchange between stream 38 flowing through one pass of the heat exchange means and the distillation vapor stream arising from separator section 118b, so that stream 38 is cooled to substantial condensation while heating the distillation vapor stream.
[0031] The resulting substantially condensed stream 38a at -138 F [-95 C] is then flash expanded through expansion valve 14 to the operating pressure (approximately 400 psia [2,758 kPa(a)]) of rectifying section 118c (an absorbing means) and absorbing section 118d (another absorbing means) inside processing assembly 118. During expansion a portion of the stream may be vaporized, resulting in cooling of the total stream. In the process illustrated in FIG. 2, the expanded stream 38b leaving expansion valve 14 reaches a temperature of -139 F [-95 C]
and is supplied to processing assembly 118 between rectifying section 118c and absorbing section 118d. The liquids in stream 38b combine with the liquids falling from rectifying section 118c and are directed to absorbing section 118d, while any vapors combine with the vapors rising from absorbing section 118d and are directed to rectifying section 118c.
[0032] The remaining 73% of the vapor from separator section 118f (stream 39) enters a work expansion machine 15 in which mechanical energy is extracted from this portion of the high pressure feed. The machine 15 expands the vapor substantially isentropically to the operating pressure of absorbing section 118d, with the work expansion cooling the expanded stream 39a to a temperature of approximately -99 F [-73 C]. The partially condensed expanded stream 39a is thereafter supplied as feed to the lower region of absorbing section 118d inside processing assembly 118.
[0033] The recompressed and cooled distillation vapor stream 41c is divided into two streams. One portion, stream 46, is the volatile residue gas product.
The other portion, recycle stream 45, enters a heat exchange means in the feed cooling section 118a inside processing assembly 118. This heat exchange means may also be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers. The heat exchange means is configured to provide heat exchange between stream 45 flowing through one pass of the heat exchange means and the distillation vapor stream arising from separator section 118b, so that stream 45 is cooled to substantial condensation while heating the distillation vapor stream.
[0034] The substantially condensed recycle stream 45a leaves the heat exchange means in feed cooling section 118a at -138 F [-95 C] and is flash expanded through expansion valve 22 to the operating pressure of rectifying section 118c inside processing assembly 118. During expansion a portion of the stream is vaporized, resulting in cooling of the total stream. In the process illustrated in FIG.
2, the expanded stream 45b leaving expansion valve 22 reaches a temperature of -146 F
[-99 C] and is supplied to separator section 118b inside processing assembly 118.
The liquids separated therein are directed to rectifying section 118c, while the remaining vapors combine with the vapors rising from rectifying section 118c to form the distillation vapor stream that is heated in cooling section 118a.
[0035] Rectifying section 118c and absorbing section 118d each contain an absorbing means consisting of a plurality of vertically spaced trays, one or more packed beds, or some combination of trays and packing. The trays and/or packing in rectifying section 118c and absorbing section 118d provide the necessary contact between the vapors rising upward and cold liquid falling downward. The liquid portion of the expanded stream 39a commingles with liquids falling downward from absorbing section 118d and the combined liquid continues downward into demethanizing section 118e. The stripping vapors arising from demethanizing section 118e combine with the vapor portion of the expanded stream 39a and rise upward through absorbing section 118d, to be contacted with the cold liquid falling downward to condense and absorb most of the C2 components, C3 components, and heavier components from these vapors. The vapors arising from absorbing section 118d combine with any vapor portion of the expanded stream 38b and rise upward through rectifying section 118c, to be contacted with the cold liquid portion of expanded stream 45b falling downward to condense and absorb most of the C2 components, C3 components, and heavier components remaining in these vapors.
The liquid portion of the expanded stream 38b commingles with liquids falling downward from rectifying section 118c and the combined liquid continues downward into absorbing section 118d.
[0036] The distillation liquid flowing downward from the heat and mass transfer means in demethanizing section 118e inside processing assembly 118 has been stripped of methane and lighter components. The resulting liquid product (stream 44) exits the lower region of demethanizing section 118e and leaves processing assembly 118 at 65 F [18 C]. The distillation vapor stream arising from separator section 118b is warmed in feed cooling section 118a as it provides cooling to streams 32, 38, and 45 as described previously, and the resulting distillation vapor stream 41 leaves processing assembly 118 at 105 F [40 C]. The distillation vapor stream is then re-compressed in two stages, compressor 16 driven by expansion machine 15 and compressor 20 driven by a supplemental power source. After stream 41b is cooled to 110 F [43 C] in discharge cooler 21 to form stream 41c, recycle stream 45 is withdrawn as described earlier, forming residue gas stream 46 which thereafter flows to the sales gas pipeline at 915 psia [6,307 kPa(a)].
[0037] A summary of stream flow rates and energy consumption for the process illustrated in FIG. 2 is set forth in the following table:
Table II
(FIG. 2) Stream Flow Summary - Lb. Moles/Hr [kg moles/Hr]
Stream Methane Ethane Propane Butanes+
Total 31 12,398 546 233 229 13,726 32 8,679 382 163 160 9,608 33 3,719 164 70 69 4,118 34 12,164 495 174 72 13,213 36 3,248 132 46 19 3,528 38 3,482 183 105 176 4,041 39 8,916 363 128 53 9,685 41 13,863 30 0 0 14,095 45 1,475 3 0 0 1,500 46 12,388 27 0 0 12,595 1,131 Recoveries*
Ethane 95.03%
Propane 99.99%
Butanes+ 100.00%
Power Residue Gas Compression 5,787 HP 9,514 kW]
* (Based on un-rounded flow rates) [0038] A comparison of Tables I and II shows that the present invention maintains essentially the same recoveries as the prior art. However, further comparison of Tables I and II shows that the product yields were achieved using significantly less power than the prior art. In terms of the recovery efficiency (defined by the quantity of ethane recovered per unit of power), the present invention represents more than a 6% improvement over the prior art of the FIG. 1 process.
[0039] The improvement in recovery efficiency provided by the present invention over that of the prior art of the FIG. 1 process is primarily due to two factors. First, the compact arrangement of the heat exchange means in feed cooling section 118a and the heat and mass transfer means in demethanizing section 118e in processing assembly 118 eliminates the pressure drop imposed by the interconnecting piping found in conventional processing plants. The result is that the portion of the feed gas flowing to expansion machine 15 is at higher pressure for the present invention compared to the prior art, allowing expansion machine 15 in the present invention to produce as much power with a higher outlet pressure as expansion machine 15 in the prior art can produce at a lower outlet pressure. Thus, rectifying section 118c and absorbing section 118d in processing assembly 118 of the present invention can operate at higher pressure than fractionation column 18 of the prior art while maintaining the same recovery level. This higher operating pressure, plus the reduction in pressure drop for the distillation vapor stream due to eliminating the interconnecting piping, results in a significantly higher pressure for the distillation vapor stream entering compressor 20, thereby reducing the power required by the present invention to restore the residue gas to pipeline pressure.
[0040] Second, using the heat and mass transfer means in demethanizing section 118e to simultaneously heat the distillation liquid leaving absorbing section 118d while allowing the resulting vapors to contact the liquid and strip its volatile components is more efficient than using a conventional distillation column with external reboilers. The volatile components are stripped out of the liquid continuously, reducing the concentration of the volatile components in the stripping vapors more quickly and thereby improving the stripping efficiency for the present invention.
[0041] The present invention offers two other advantages over the prior art in addition to the increase in processing efficiency. First, the compact arrangement of processing assembly 118 of the present invention replaces five separate equipment items in the prior art (heat exchangers 10, 11, and 13; separator 12; and fractionation tower 18 in FIG. 1) with a single equipment item (processing assembly 118 in FIG. 2). This reduces the plot space requirements and eliminates the interconnecting piping, reducing the capital cost of a process plant utilizing the present invention over that of the prior art. Second, elimination of the interconnecting piping means that a processing plant utilizing the present invention has far fewer flanged connections compared to the prior art, reducing the number of potential leak sources in the plant.
Hydrocarbons are volatile organic compounds (VOCs), some of which are classified as greenhouse gases and some of which may be precursors to atmospheric ozone formation, which means the present invention reduces the potential for atmospheric releases that can damage the environment.
Other Embodiments [0042] Some circumstances may favor eliminating feed cooling section 118a from processing assembly 118, and using a heat exchange means external to the processing assembly for feed cooling, such as heat exchanger 10 shown in FIGS.
through 17. Such an arrangement allows processing assembly 118 to be smaller, which may reduce the overall plant cost and/or shorten the fabrication schedule in some cases. Note that in all cases exchanger 10 is representative of either a multitude of individual heat exchangers or a single multi-pass heat exchanger, or any combination thereof. Each such heat exchanger may be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers.
[0043] Some circumstances may favor supplying liquid stream 35 directly to the lower region of absorbing section 118d via stream 40 as shown in FIGS. 2, 4, 6, 8, 10, 12, 14, and 16. In such cases, an appropriate expansion device (such as expansion valve 17) is used to expand the liquid to the operating pressure of absorbing section 118d and the resulting expanded liquid stream 40a is supplied as feed to the lower region of absorbing section 118d (as shown by the dashed lines). Some circumstances may favor combining a portion of liquid stream 35 (stream 37) with the vapor in stream 36 (FIGS. 2, 6, 10, and 14) or with cooled second portion 33a (FIGS. 4, 8, 12, and 16) to form combined stream 38 and routing the remaining portion of liquid stream 35 to the lower region of absorbing section 118d via streams 40/40a. Some circumstances may favor combining the expanded liquid stream 40a with expanded stream 39a (FIGS. 2, 6, 10, and 14) or expanded stream 34a (FIGS. 4, 8, 12, and 16) and thereafter supplying the combined stream to the lower region of absorbing section 118d as a single feed.
[0044] If the feed gas is richer, the quantity of liquid separated in stream 35 may be great enough to favor placing an additional mass transfer zone in demethanizing section 118e between expanded stream 39a and expanded liquid stream 40a as shown in FIGS. 3, 7, 11, and 15, or between expanded stream 34a and expanded liquid stream 40a as shown in FIGS. 5, 9, 13, and 17. In such cases, the heat and mass transfer means in demethanizing section 118e may be configured in upper and lower parts so that expanded liquid stream 40a can be introduced between the two parts. As shown by the dashed lines, some circumstances may favor combining a portion of liquid stream 35 (stream 37) with the vapor in stream (FIGS. 3, 7, 11, and 15) or with cooled second portion 33a (FIGS. 5, 9, 13, and 17) to form combined stream 38, while the remaining portion of liquid stream 35 (stream 40) is expanded to lower pressure and supplied between the upper and lower parts of the heat and mass transfer means in demethanizing section 118e as stream 40a.
[0045] Some circumstances may favor not combining the cooled first and second portions (streams 32a and 33a) as shown in FIGS. 4, 5, 8, 9, 12, 13, 16, and 17. In such cases, only the cooled first portion 32a is directed to separator section 118f inside processing assembly 118 (FIGS. 4, 5, 12, and 13) or separator 12 (FIGS. 8, 9, 16, and 17) where the vapor (stream 34) is separated from the condensed liquid (stream 35). Vapor stream 34 enters work expansion machine 15 and is expanded substantially isentropically to the operating pressure of absorbing section 118d, whereupon expanded stream 34a is supplied as feed to the lower region of absorbing section 118d inside processing assembly 118. The cooled second portion 33a is combined with the separated liquid (stream 35, via stream 37), and the combined stream 38 is directed to the heat exchange means in the lower region of feed cooling section 118a inside processing assembly 118 (or in heat exchanger external to processing assembly 118) and cooled to substantial condensation.
The substantially condensed stream 38a is flash expanded through expansion valve 14 to the operating pressure of rectifying section 118c and absorbing section 118d, whereupon expanded stream 38b is supplied to processing assembly 118 between rectifying section 118c and absorbing section 118d. Some circumstances may favor combining only a portion (stream 37) of liquid stream 35 with the cooled second portion 33a, with the remaining portion (stream 40) supplied to the lower region of absorbing section 118c1 via expansion valve 17. Other circumstances may favor sending all of liquid stream 35 to the lower region of absorbing section 118d via expansion valve 17.
[0046] In some circumstances, it may be advantageous to use an external separator vessel to separate cooled feed stream 31a or cooled first portion 32a, rather than including separator section 118f in processing assembly 118. As shown in FIGS. 6, 7, 14, and 15, separator 12 can be used to separate cooled feed stream 31a into vapor stream 34 and liquid stream 35. Likewise, as shown in FIGS. 8, 9, 16, and 17, separator 12 can be used to separate cooled first portion 32a into vapor stream 34 and liquid stream 35.
[0047] Depending on the quantity of heavier hydrocarbons in the feed gas and the feed gas pressure, the cooled feed stream 31a entering separator section 118f in
10024] The liquid product stream 44 exits the bottom of the tower at [18 C], based on a typical specification of a methane to ethane ratio of 0.010:1 on a mass basis in the bottom product. The demethanizer overhead vapor stream 41 passes countercurrently to the incoming feed gas and recycle stream in heat exchanger where it is heated to -40 F [-40 C] (stream 41a) and in heat exchanger 10 where it is heated to 104 F [40 C] (stream 41b). The distillation vapor stream is then re-compressed in two stages. The first stage is compressor 16 driven by expansion machine 15. The second stage is compressor 20 driven by a supplemental power source which compresses the residue gas (stream 41d) to sales line pressure.
After cooling to 110 F [43 C] in discharge cooler 21, stream 41e is split into the residue gas product (stream 46) and the recycle stream 45 as described earlier. Residue gas stream 46 flows to the sales gas pipeline at 915 psia [6,307 kPa(a)], sufficient to meet line requirements (usually on the order of the inlet pressure).
[0025] A summary of stream flow rates and energy consumption for the process illustrated in FIG. 1 is set forth in the following table:
Table I
(FIG. 1) Stream Flow Summary - Lb. Moles/Hr [kg moles/Hr]
Stream Methane Ethane Propane Butanes+
Total 31 12,398 546 233 229 13,726 32 8,431 371 159 156 9,334 33 3,967 175 74 73 4,392 34 12,195 501 179 77 13,261 36 3,317 136 49 21 3,607 38 3,520 181 103 173 4,072 39 8,878 365 130 56 9,654 41 13,765 30 0 0 13,992 45 1,377 3 0 0 1,400 46 12,388 27 0 0 12,592 1,134 Recoveries*
Ethane 94.99%
Propane 99.99%
Butanes+ 100.00%
Power Residue Gas Compression 6,149 HP [
10,109 kW]
* (Based on un-rounded flow rates) DESCRIPTION OF THE INVENTION
[00261 FIG. 2 illustrates a flow diagram of a process in accordance with the present invention. The feed gas composition and conditions considered in the process presented in FIG. 2 are the same as those in FIG. 1. Accordingly, the FIG. 2 process can be compared with that of the FIG. 1 process to illustrate the advantages of the present invention.
[00271 In the simulation of the FIG. 2 process, inlet gas enters the plant as stream 31 and is divided into two portions, streams 32 and 33. The first portion, stream 32, enters a heat exchange means in the upper region of feed cooling section 118a inside processing assembly 118. This heat exchange means may be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers. The heat exchange means is configured to provide heat exchange between stream 32 flowing through one pass of the heat exchange means and a distillation vapor stream arising from separator section 118b inside processing assembly 118 that has been heated in a heat exchange means in the lower region of feed cooling section 118a. Stream 32 is cooled while further heating the distillation vapor stream, with stream 32a leaving the heat exchange means at -[-32 C].
[0028] The second portion, stream 33, enters a heat and mass transfer means in demethanizing section 118e inside processing assembly 118. This heat and mass transfer means may also be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers.
The heat and mass transfer means is configured to provide heat exchange between stream flowing through one pass of the heat and mass transfer means and a distillation liquid stream flowing downward from absorbing section 118d inside processing assembly 118, so that stream 33 is cooled while heating the distillation liquid stream, cooling stream 33a to -47 F [-44 C] before it leaves the heat and mass transfer means.
As the distillation liquid stream is heated, a portion of it is vaporized to form stripping vapors that rise upward as the remaining liquid continues flowing downward through the heat and mass transfer means. The heat and mass transfer means provides continuous contact between the stripping vapors and the distillation liquid stream so that it also functions to provide mass transfer between the vapor and liquid phases, stripping the liquid product stream 44 of methane and lighter components.
[0029] Streams 32a and 33a recombine to form stream 31a, which enters separator section 118f inside processing assembly 118 at -32 F [-36 C] and 900 psia [6,203 kPa(a)], whereupon the vapor (stream 34) is separated from the condensed liquid (stream 35). Separator section 118f has an internal head or other means to divide it from demethanizing section 118e, so that the two sections inside processing assembly 118 can operate at different pressures.
[0030] The vapor (stream 34) from separator section 118f is divided into two streams, 36 and 39. Stream 36, containing about 27% of the total vapor, is combined with the separated liquid (stream 35, via stream 37), and the combined stream enters a heat exchange means in the lower region of feed cooling section 118a inside processing assembly 118. This heat exchange means may likewise be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers. The heat exchange means is configured to provide heat exchange between stream 38 flowing through one pass of the heat exchange means and the distillation vapor stream arising from separator section 118b, so that stream 38 is cooled to substantial condensation while heating the distillation vapor stream.
[0031] The resulting substantially condensed stream 38a at -138 F [-95 C] is then flash expanded through expansion valve 14 to the operating pressure (approximately 400 psia [2,758 kPa(a)]) of rectifying section 118c (an absorbing means) and absorbing section 118d (another absorbing means) inside processing assembly 118. During expansion a portion of the stream may be vaporized, resulting in cooling of the total stream. In the process illustrated in FIG. 2, the expanded stream 38b leaving expansion valve 14 reaches a temperature of -139 F [-95 C]
and is supplied to processing assembly 118 between rectifying section 118c and absorbing section 118d. The liquids in stream 38b combine with the liquids falling from rectifying section 118c and are directed to absorbing section 118d, while any vapors combine with the vapors rising from absorbing section 118d and are directed to rectifying section 118c.
[0032] The remaining 73% of the vapor from separator section 118f (stream 39) enters a work expansion machine 15 in which mechanical energy is extracted from this portion of the high pressure feed. The machine 15 expands the vapor substantially isentropically to the operating pressure of absorbing section 118d, with the work expansion cooling the expanded stream 39a to a temperature of approximately -99 F [-73 C]. The partially condensed expanded stream 39a is thereafter supplied as feed to the lower region of absorbing section 118d inside processing assembly 118.
[0033] The recompressed and cooled distillation vapor stream 41c is divided into two streams. One portion, stream 46, is the volatile residue gas product.
The other portion, recycle stream 45, enters a heat exchange means in the feed cooling section 118a inside processing assembly 118. This heat exchange means may also be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers. The heat exchange means is configured to provide heat exchange between stream 45 flowing through one pass of the heat exchange means and the distillation vapor stream arising from separator section 118b, so that stream 45 is cooled to substantial condensation while heating the distillation vapor stream.
[0034] The substantially condensed recycle stream 45a leaves the heat exchange means in feed cooling section 118a at -138 F [-95 C] and is flash expanded through expansion valve 22 to the operating pressure of rectifying section 118c inside processing assembly 118. During expansion a portion of the stream is vaporized, resulting in cooling of the total stream. In the process illustrated in FIG.
2, the expanded stream 45b leaving expansion valve 22 reaches a temperature of -146 F
[-99 C] and is supplied to separator section 118b inside processing assembly 118.
The liquids separated therein are directed to rectifying section 118c, while the remaining vapors combine with the vapors rising from rectifying section 118c to form the distillation vapor stream that is heated in cooling section 118a.
[0035] Rectifying section 118c and absorbing section 118d each contain an absorbing means consisting of a plurality of vertically spaced trays, one or more packed beds, or some combination of trays and packing. The trays and/or packing in rectifying section 118c and absorbing section 118d provide the necessary contact between the vapors rising upward and cold liquid falling downward. The liquid portion of the expanded stream 39a commingles with liquids falling downward from absorbing section 118d and the combined liquid continues downward into demethanizing section 118e. The stripping vapors arising from demethanizing section 118e combine with the vapor portion of the expanded stream 39a and rise upward through absorbing section 118d, to be contacted with the cold liquid falling downward to condense and absorb most of the C2 components, C3 components, and heavier components from these vapors. The vapors arising from absorbing section 118d combine with any vapor portion of the expanded stream 38b and rise upward through rectifying section 118c, to be contacted with the cold liquid portion of expanded stream 45b falling downward to condense and absorb most of the C2 components, C3 components, and heavier components remaining in these vapors.
The liquid portion of the expanded stream 38b commingles with liquids falling downward from rectifying section 118c and the combined liquid continues downward into absorbing section 118d.
[0036] The distillation liquid flowing downward from the heat and mass transfer means in demethanizing section 118e inside processing assembly 118 has been stripped of methane and lighter components. The resulting liquid product (stream 44) exits the lower region of demethanizing section 118e and leaves processing assembly 118 at 65 F [18 C]. The distillation vapor stream arising from separator section 118b is warmed in feed cooling section 118a as it provides cooling to streams 32, 38, and 45 as described previously, and the resulting distillation vapor stream 41 leaves processing assembly 118 at 105 F [40 C]. The distillation vapor stream is then re-compressed in two stages, compressor 16 driven by expansion machine 15 and compressor 20 driven by a supplemental power source. After stream 41b is cooled to 110 F [43 C] in discharge cooler 21 to form stream 41c, recycle stream 45 is withdrawn as described earlier, forming residue gas stream 46 which thereafter flows to the sales gas pipeline at 915 psia [6,307 kPa(a)].
[0037] A summary of stream flow rates and energy consumption for the process illustrated in FIG. 2 is set forth in the following table:
Table II
(FIG. 2) Stream Flow Summary - Lb. Moles/Hr [kg moles/Hr]
Stream Methane Ethane Propane Butanes+
Total 31 12,398 546 233 229 13,726 32 8,679 382 163 160 9,608 33 3,719 164 70 69 4,118 34 12,164 495 174 72 13,213 36 3,248 132 46 19 3,528 38 3,482 183 105 176 4,041 39 8,916 363 128 53 9,685 41 13,863 30 0 0 14,095 45 1,475 3 0 0 1,500 46 12,388 27 0 0 12,595 1,131 Recoveries*
Ethane 95.03%
Propane 99.99%
Butanes+ 100.00%
Power Residue Gas Compression 5,787 HP 9,514 kW]
* (Based on un-rounded flow rates) [0038] A comparison of Tables I and II shows that the present invention maintains essentially the same recoveries as the prior art. However, further comparison of Tables I and II shows that the product yields were achieved using significantly less power than the prior art. In terms of the recovery efficiency (defined by the quantity of ethane recovered per unit of power), the present invention represents more than a 6% improvement over the prior art of the FIG. 1 process.
[0039] The improvement in recovery efficiency provided by the present invention over that of the prior art of the FIG. 1 process is primarily due to two factors. First, the compact arrangement of the heat exchange means in feed cooling section 118a and the heat and mass transfer means in demethanizing section 118e in processing assembly 118 eliminates the pressure drop imposed by the interconnecting piping found in conventional processing plants. The result is that the portion of the feed gas flowing to expansion machine 15 is at higher pressure for the present invention compared to the prior art, allowing expansion machine 15 in the present invention to produce as much power with a higher outlet pressure as expansion machine 15 in the prior art can produce at a lower outlet pressure. Thus, rectifying section 118c and absorbing section 118d in processing assembly 118 of the present invention can operate at higher pressure than fractionation column 18 of the prior art while maintaining the same recovery level. This higher operating pressure, plus the reduction in pressure drop for the distillation vapor stream due to eliminating the interconnecting piping, results in a significantly higher pressure for the distillation vapor stream entering compressor 20, thereby reducing the power required by the present invention to restore the residue gas to pipeline pressure.
[0040] Second, using the heat and mass transfer means in demethanizing section 118e to simultaneously heat the distillation liquid leaving absorbing section 118d while allowing the resulting vapors to contact the liquid and strip its volatile components is more efficient than using a conventional distillation column with external reboilers. The volatile components are stripped out of the liquid continuously, reducing the concentration of the volatile components in the stripping vapors more quickly and thereby improving the stripping efficiency for the present invention.
[0041] The present invention offers two other advantages over the prior art in addition to the increase in processing efficiency. First, the compact arrangement of processing assembly 118 of the present invention replaces five separate equipment items in the prior art (heat exchangers 10, 11, and 13; separator 12; and fractionation tower 18 in FIG. 1) with a single equipment item (processing assembly 118 in FIG. 2). This reduces the plot space requirements and eliminates the interconnecting piping, reducing the capital cost of a process plant utilizing the present invention over that of the prior art. Second, elimination of the interconnecting piping means that a processing plant utilizing the present invention has far fewer flanged connections compared to the prior art, reducing the number of potential leak sources in the plant.
Hydrocarbons are volatile organic compounds (VOCs), some of which are classified as greenhouse gases and some of which may be precursors to atmospheric ozone formation, which means the present invention reduces the potential for atmospheric releases that can damage the environment.
Other Embodiments [0042] Some circumstances may favor eliminating feed cooling section 118a from processing assembly 118, and using a heat exchange means external to the processing assembly for feed cooling, such as heat exchanger 10 shown in FIGS.
through 17. Such an arrangement allows processing assembly 118 to be smaller, which may reduce the overall plant cost and/or shorten the fabrication schedule in some cases. Note that in all cases exchanger 10 is representative of either a multitude of individual heat exchangers or a single multi-pass heat exchanger, or any combination thereof. Each such heat exchanger may be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers.
[0043] Some circumstances may favor supplying liquid stream 35 directly to the lower region of absorbing section 118d via stream 40 as shown in FIGS. 2, 4, 6, 8, 10, 12, 14, and 16. In such cases, an appropriate expansion device (such as expansion valve 17) is used to expand the liquid to the operating pressure of absorbing section 118d and the resulting expanded liquid stream 40a is supplied as feed to the lower region of absorbing section 118d (as shown by the dashed lines). Some circumstances may favor combining a portion of liquid stream 35 (stream 37) with the vapor in stream 36 (FIGS. 2, 6, 10, and 14) or with cooled second portion 33a (FIGS. 4, 8, 12, and 16) to form combined stream 38 and routing the remaining portion of liquid stream 35 to the lower region of absorbing section 118d via streams 40/40a. Some circumstances may favor combining the expanded liquid stream 40a with expanded stream 39a (FIGS. 2, 6, 10, and 14) or expanded stream 34a (FIGS. 4, 8, 12, and 16) and thereafter supplying the combined stream to the lower region of absorbing section 118d as a single feed.
[0044] If the feed gas is richer, the quantity of liquid separated in stream 35 may be great enough to favor placing an additional mass transfer zone in demethanizing section 118e between expanded stream 39a and expanded liquid stream 40a as shown in FIGS. 3, 7, 11, and 15, or between expanded stream 34a and expanded liquid stream 40a as shown in FIGS. 5, 9, 13, and 17. In such cases, the heat and mass transfer means in demethanizing section 118e may be configured in upper and lower parts so that expanded liquid stream 40a can be introduced between the two parts. As shown by the dashed lines, some circumstances may favor combining a portion of liquid stream 35 (stream 37) with the vapor in stream (FIGS. 3, 7, 11, and 15) or with cooled second portion 33a (FIGS. 5, 9, 13, and 17) to form combined stream 38, while the remaining portion of liquid stream 35 (stream 40) is expanded to lower pressure and supplied between the upper and lower parts of the heat and mass transfer means in demethanizing section 118e as stream 40a.
[0045] Some circumstances may favor not combining the cooled first and second portions (streams 32a and 33a) as shown in FIGS. 4, 5, 8, 9, 12, 13, 16, and 17. In such cases, only the cooled first portion 32a is directed to separator section 118f inside processing assembly 118 (FIGS. 4, 5, 12, and 13) or separator 12 (FIGS. 8, 9, 16, and 17) where the vapor (stream 34) is separated from the condensed liquid (stream 35). Vapor stream 34 enters work expansion machine 15 and is expanded substantially isentropically to the operating pressure of absorbing section 118d, whereupon expanded stream 34a is supplied as feed to the lower region of absorbing section 118d inside processing assembly 118. The cooled second portion 33a is combined with the separated liquid (stream 35, via stream 37), and the combined stream 38 is directed to the heat exchange means in the lower region of feed cooling section 118a inside processing assembly 118 (or in heat exchanger external to processing assembly 118) and cooled to substantial condensation.
The substantially condensed stream 38a is flash expanded through expansion valve 14 to the operating pressure of rectifying section 118c and absorbing section 118d, whereupon expanded stream 38b is supplied to processing assembly 118 between rectifying section 118c and absorbing section 118d. Some circumstances may favor combining only a portion (stream 37) of liquid stream 35 with the cooled second portion 33a, with the remaining portion (stream 40) supplied to the lower region of absorbing section 118c1 via expansion valve 17. Other circumstances may favor sending all of liquid stream 35 to the lower region of absorbing section 118d via expansion valve 17.
[0046] In some circumstances, it may be advantageous to use an external separator vessel to separate cooled feed stream 31a or cooled first portion 32a, rather than including separator section 118f in processing assembly 118. As shown in FIGS. 6, 7, 14, and 15, separator 12 can be used to separate cooled feed stream 31a into vapor stream 34 and liquid stream 35. Likewise, as shown in FIGS. 8, 9, 16, and 17, separator 12 can be used to separate cooled first portion 32a into vapor stream 34 and liquid stream 35.
[0047] Depending on the quantity of heavier hydrocarbons in the feed gas and the feed gas pressure, the cooled feed stream 31a entering separator section 118f in
-24-FIGS. 2, 3, 10, and 11 or separator 12 in FIGS. 6, 7, 14, and 15 (or the cooled first portion 32a entering separator section 118f in FIGS. 4, 5, 12, and 13 or separator 12 in FIGS. 8, 9, 16, and 17) may not contain any liquid (because it is above its dewpoint, or because it is above its cricondenbar). In such cases, there is no liquid in streams 35 and 37 (as shown by the dashed lines), so only the vapor from separator section 118f in stream 36 (FIGS. 2, 3, 10, and 11), the vapor from separator 12 in stream 36 (FIGS. 6, 7, 14, and 15), or the cooled second portion 33a (FIGS. 4, 5, 8, 9, 12, 13, 16, and 17) flows to stream 38 to become the expanded substantially condensed stream 38b supplied to processing assembly 118 between rectifying section 118c and absorbing section 118d. In such circumstances, separator section 118f in processing assembly 118 (FIGS. 2 through 5 and 10 through 13) or separator 12 (FIGS. 6 through 9 and 14 through 17) may not be required.
[0048] Feed gas conditions, plant size, available equipment, or other factors may indicate that elimination of work expansion machine 15, or replacement with an alternate expansion device (such as an expansion valve), is feasible. Although individual stream expansion is depicted in particular expansion devices, alternative expansion means may be employed where appropriate. For example, conditions may warrant work expansion of the substantially condensed portion of the feed stream (stream 38a) or the substantially condensed recycle stream (stream 45a).
[0049] In accordance with the present invention, the use of external refrigeration to supplement the cooling available to the inlet gas from the distillation vapor and liquid streams may be employed, particularly in the case of a rich inlet gas.
In such cases, a heat and mass transfer means may be included in separator section 118f (or a gas collecting means in such cases when the cooled feed stream 31a or the cooled first portion 32a contains no liquid) as shown by the dashed lines in FIGS. 2
[0048] Feed gas conditions, plant size, available equipment, or other factors may indicate that elimination of work expansion machine 15, or replacement with an alternate expansion device (such as an expansion valve), is feasible. Although individual stream expansion is depicted in particular expansion devices, alternative expansion means may be employed where appropriate. For example, conditions may warrant work expansion of the substantially condensed portion of the feed stream (stream 38a) or the substantially condensed recycle stream (stream 45a).
[0049] In accordance with the present invention, the use of external refrigeration to supplement the cooling available to the inlet gas from the distillation vapor and liquid streams may be employed, particularly in the case of a rich inlet gas.
In such cases, a heat and mass transfer means may be included in separator section 118f (or a gas collecting means in such cases when the cooled feed stream 31a or the cooled first portion 32a contains no liquid) as shown by the dashed lines in FIGS. 2
-25-through 5 and 10 through 13, or a heat and mass transfer means may be included in separator 12 as shown by the dashed lines in FIGS. 6 though 9 and 14 through 17.
This heat and mass transfer means may be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers. The heat and mass transfer means is configured to provide heat exchange between a refrigerant stream (e.g., propane) flowing through one pass of the heat and mass transfer means and the vapor portion of stream 31a (FIGS. 2, 3, 6, 7, 10, 11, 14, and 15) or stream 32a (FIGS. 4, 5, 8, 9, 12, 13, 16, and 17) flowing upward, so that the refrigerant further cools the vapor and condenses additional liquid, which falls downward to become part of the liquid removed in stream 35. Alternatively, conventional gas chiller(s) could be used to cool stream 32a, stream 33a, and/or stream 31a with refrigerant before stream 31a enters separator section 118f (FIGS. 2, 3, 10, and 11) or separator 12 (FIGS. 6, 7, 14, and 15) or stream 32a enters separator section 118f (FIGS. 4, 5, 12, and 13) or separator 12 (FIGS. 8, 9, 16, and 17).
[0050] Depending on the temperature and richness of the feed gas and the amount of C2 components to be recovered in liquid product stream 44, there may not be sufficient heating available from stream 33 to cause the liquid leaving demethanizing section 118e to meet the product specifications. In such cases, the heat and mass transfer means in demethanizing section 118e may include provisions for providing supplemental heating with heating medium as shown by the dashed lines in FIGS. 2 through 17. Alternatively, another heat and mass transfer means can be included in the lower region of demethanizing section 118e for providing supplemental heating, or stream 33 can be heated with heating medium before it is supplied to the heat and mass transfer means in demethanizing section 118e.
This heat and mass transfer means may be comprised of a fin and tube type heat exchanger, a plate type heat exchanger, a brazed aluminum type heat exchanger, or other type of heat transfer device, including multi-pass and/or multi-service heat exchangers. The heat and mass transfer means is configured to provide heat exchange between a refrigerant stream (e.g., propane) flowing through one pass of the heat and mass transfer means and the vapor portion of stream 31a (FIGS. 2, 3, 6, 7, 10, 11, 14, and 15) or stream 32a (FIGS. 4, 5, 8, 9, 12, 13, 16, and 17) flowing upward, so that the refrigerant further cools the vapor and condenses additional liquid, which falls downward to become part of the liquid removed in stream 35. Alternatively, conventional gas chiller(s) could be used to cool stream 32a, stream 33a, and/or stream 31a with refrigerant before stream 31a enters separator section 118f (FIGS. 2, 3, 10, and 11) or separator 12 (FIGS. 6, 7, 14, and 15) or stream 32a enters separator section 118f (FIGS. 4, 5, 12, and 13) or separator 12 (FIGS. 8, 9, 16, and 17).
[0050] Depending on the temperature and richness of the feed gas and the amount of C2 components to be recovered in liquid product stream 44, there may not be sufficient heating available from stream 33 to cause the liquid leaving demethanizing section 118e to meet the product specifications. In such cases, the heat and mass transfer means in demethanizing section 118e may include provisions for providing supplemental heating with heating medium as shown by the dashed lines in FIGS. 2 through 17. Alternatively, another heat and mass transfer means can be included in the lower region of demethanizing section 118e for providing supplemental heating, or stream 33 can be heated with heating medium before it is supplied to the heat and mass transfer means in demethanizing section 118e.
-26-, =
100511 Depending on the type of heat transfer devices selected for the heat exchange means in the upper and lower regions of feed cooling section 118a, it may be possible to combine these heat exchange means in a single multi-pass and/or multi-service heat transfer device. In such cases, the multi-pass and/or multi-service heat transfer device will include appropriate means for distributing, segregating, and collecting stream 32, stream 38, stream 45, and the distillation vapor stream in order to accomplish the desired cooling and heating.
100521 Some circumstances may favor providing additional mass transfer in the upper region of demethanizing section 118e. In such cases, a mass transfer means can be located below where expanded stream 39a (FIGS. 2, 3, 6, 7, 10, 11, 14, and 15) or expanded stream 34a (FIGS. 4, 5, 8, 9, 12, 13, 16, and 17) enters the lower region of absorbing section 118d and above where cooled second portion 33a leaves the heat and mass transfer means in demethanizing section 118e.
100531 A less preferred option for the FIGS. 2, 3, 6, 7, 10, 11, 14, and 15 embodiments of the present invention is providing a separator vessel for cooled first portion 32a, a separator vessel for cooled second portion 33a, combining the vapor streams separated therein to form vapor stream 34, and combining the liquid streams separated therein to form liquid stream 35. Another less preferred option for the present invention is cooling stream 37 in a separate heat exchange means inside feed cooling section 118a in FIGS. 2, 3, 4, 5, 6, 7, 8, and 9 or a separate pass in heat exchanger 10 in FIGS. 10, 11, 12, 13, 14, 15, 16, and 17 (rather than combining stream 37 with stream 36 or stream 33a to form combined stream 38), expanding the cooled stream in a separate expansion device, and supplying the expanded stream to an intermediate region in absorbing section 118d.
100511 Depending on the type of heat transfer devices selected for the heat exchange means in the upper and lower regions of feed cooling section 118a, it may be possible to combine these heat exchange means in a single multi-pass and/or multi-service heat transfer device. In such cases, the multi-pass and/or multi-service heat transfer device will include appropriate means for distributing, segregating, and collecting stream 32, stream 38, stream 45, and the distillation vapor stream in order to accomplish the desired cooling and heating.
100521 Some circumstances may favor providing additional mass transfer in the upper region of demethanizing section 118e. In such cases, a mass transfer means can be located below where expanded stream 39a (FIGS. 2, 3, 6, 7, 10, 11, 14, and 15) or expanded stream 34a (FIGS. 4, 5, 8, 9, 12, 13, 16, and 17) enters the lower region of absorbing section 118d and above where cooled second portion 33a leaves the heat and mass transfer means in demethanizing section 118e.
100531 A less preferred option for the FIGS. 2, 3, 6, 7, 10, 11, 14, and 15 embodiments of the present invention is providing a separator vessel for cooled first portion 32a, a separator vessel for cooled second portion 33a, combining the vapor streams separated therein to form vapor stream 34, and combining the liquid streams separated therein to form liquid stream 35. Another less preferred option for the present invention is cooling stream 37 in a separate heat exchange means inside feed cooling section 118a in FIGS. 2, 3, 4, 5, 6, 7, 8, and 9 or a separate pass in heat exchanger 10 in FIGS. 10, 11, 12, 13, 14, 15, 16, and 17 (rather than combining stream 37 with stream 36 or stream 33a to form combined stream 38), expanding the cooled stream in a separate expansion device, and supplying the expanded stream to an intermediate region in absorbing section 118d.
-27-100541 It will be recognized that the relative amount of feed found in each branch of the split vapor feed will depend on several factors, including gas pressure, feed gas composition, the amount of heat which can economically be extracted from the feed, and the quantity of horsepower available. More feed above absorbing section 118d may increase recovery while decreasing power recovered from the expander and thereby increasing the recompression horsepower requirements.
Increasing feed below absorbing section 118d reduces the horsepower consumption but may also reduce product recovery.
100551 The present invention provides improved recovery of C2 components, C3 components, and heavier hydrocarbon components or of C3 components and heavier hydrocarbon components per amount of utility consumption required to operate the process. An improvement in utility consumption required for operating the process may appear in the form of reduced power requirements for compression or re-compression, reduced power requirements for external refrigeration, reduced energy requirements for supplemental heating, or a combination thereof.
100561 While there have been described what are believed to be preferred embodiments of the invention, those skilled in the art will recognize that other and further modifications may be made thereto, e.g. to adapt the invention to various conditions, types of feed, or other requirements.
Increasing feed below absorbing section 118d reduces the horsepower consumption but may also reduce product recovery.
100551 The present invention provides improved recovery of C2 components, C3 components, and heavier hydrocarbon components or of C3 components and heavier hydrocarbon components per amount of utility consumption required to operate the process. An improvement in utility consumption required for operating the process may appear in the form of reduced power requirements for compression or re-compression, reduced power requirements for external refrigeration, reduced energy requirements for supplemental heating, or a combination thereof.
100561 While there have been described what are believed to be preferred embodiments of the invention, those skilled in the art will recognize that other and further modifications may be made thereto, e.g. to adapt the invention to various conditions, types of feed, or other requirements.
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Claims (38)
1. A process for the separation of a gas stream containing methane, C2 components, C3 components, and heavier hydrocarbon components into a volatile residue gas fraction and a relatively less volatile fraction containing a major portion of said C2 components, C3 components, and heavier hydrocarbon components or said C3 components and heavier hydrocarbon components wherein (1) said gas stream is divided into first and second portions;
(2) said first portion is cooled;
(3) said second portion is cooled;
(4) said cooled first portion is combined with said cooled second portion to form a cooled gas stream;
(5) said cooled gas stream is divided into first and second streams;
(6) said first stream is cooled to condense substantially all of said first stream and is thereafter expanded to lower pressure whereby said first stream is further cooled;
(7) said expanded cooled first stream is supplied as a feed between first and second absorbing means housed in a single equipment item processing assembly, said first absorbing means being located above said second absorbing means;
(8) said second stream is expanded to said lower pressure and is supplied as a bottom feed to said second absorbing means;
(9) a distillation vapor stream is collected from an upper region of said first absorbing means and heated;
(10) said heated distillation vapor stream is compressed to higher pressure and thereafter divided into said volatile residue gas fraction and a compressed recycle stream;
(11) said compressed recycle stream is cooled to condense substantially all of said compressed recycle stream;
(12) said substantially condensed compressed recycle stream is expanded to said lower pressure and supplied as a top feed to said first absorbing means;
(13) said heating of said distillation vapor stream is accomplished in one or more heat exchange means, thereby to supply at least a portion of the cooling of steps (2), (6), and (11);
(14) a distillation liquid stream is collected from a lower region of said second absorbing means and heated in a heat and mass transfer means housed in said processing assembly, thereby to supply at least a portion of the cooling of step (3) while simultaneously stripping the more volatile components from said distillation liquid stream, and thereafter discharging said heated and stripped distillation liquid stream from said processing assembly as said relatively less volatile fraction; and (15) the quantities and temperatures of said feed streams to said first and second absorbing means are effective to maintain the temperature of said upper region of said first absorbing means at a temperature whereby the major portions of the components in said relatively less volatile fraction are recovered.
(2) said first portion is cooled;
(3) said second portion is cooled;
(4) said cooled first portion is combined with said cooled second portion to form a cooled gas stream;
(5) said cooled gas stream is divided into first and second streams;
(6) said first stream is cooled to condense substantially all of said first stream and is thereafter expanded to lower pressure whereby said first stream is further cooled;
(7) said expanded cooled first stream is supplied as a feed between first and second absorbing means housed in a single equipment item processing assembly, said first absorbing means being located above said second absorbing means;
(8) said second stream is expanded to said lower pressure and is supplied as a bottom feed to said second absorbing means;
(9) a distillation vapor stream is collected from an upper region of said first absorbing means and heated;
(10) said heated distillation vapor stream is compressed to higher pressure and thereafter divided into said volatile residue gas fraction and a compressed recycle stream;
(11) said compressed recycle stream is cooled to condense substantially all of said compressed recycle stream;
(12) said substantially condensed compressed recycle stream is expanded to said lower pressure and supplied as a top feed to said first absorbing means;
(13) said heating of said distillation vapor stream is accomplished in one or more heat exchange means, thereby to supply at least a portion of the cooling of steps (2), (6), and (11);
(14) a distillation liquid stream is collected from a lower region of said second absorbing means and heated in a heat and mass transfer means housed in said processing assembly, thereby to supply at least a portion of the cooling of step (3) while simultaneously stripping the more volatile components from said distillation liquid stream, and thereafter discharging said heated and stripped distillation liquid stream from said processing assembly as said relatively less volatile fraction; and (15) the quantities and temperatures of said feed streams to said first and second absorbing means are effective to maintain the temperature of said upper region of said first absorbing means at a temperature whereby the major portions of the components in said relatively less volatile fraction are recovered.
2. The process according to claim 1 wherein (a) said cooled first portion is combined with said cooled second portion to form a partially condensed gas stream;
(b) said partially condensed gas stream is supplied to a separating means and is separated therein to provide a vapor stream and at least one liquid stream;
(c) said vapor stream is divided into said first and second streams; and (d) at least a portion of said at least one liquid stream is expanded to said lower pressure and is supplied as an additional bottom feed to said second absorbing means.
(b) said partially condensed gas stream is supplied to a separating means and is separated therein to provide a vapor stream and at least one liquid stream;
(c) said vapor stream is divided into said first and second streams; and (d) at least a portion of said at least one liquid stream is expanded to said lower pressure and is supplied as an additional bottom feed to said second absorbing means.
3. The process according to claim 2 wherein (a) said first stream is combined with at least a portion of said at least one liquid stream to form a combined stream;
(b) said combined stream is cooled to condense substantially all of said combined stream and is thereafter expanded to lower pressure whereby said combined stream is further cooled;
(c) said expanded cooled combined stream is supplied as said feed between said first and second absorbing means; and (d) any remaining portion of said at least one liquid stream is expanded to said lower pressure and is supplied as said additional bottom feed to said second absorbing means.
(b) said combined stream is cooled to condense substantially all of said combined stream and is thereafter expanded to lower pressure whereby said combined stream is further cooled;
(c) said expanded cooled combined stream is supplied as said feed between said first and second absorbing means; and (d) any remaining portion of said at least one liquid stream is expanded to said lower pressure and is supplied as said additional bottom feed to said second absorbing means.
4. The process according to claim 1 wherein (a) said first portion is cooled and is thereafter expanded to lower pressure;
(b) said second portion is cooled to condense substantially all of said second portion and is thereafter expanded to said lower pressure whereby said second portion is further cooled;
(c) said expanded cooled second portion is supplied as said feed between said first and second absorbing means; and (d) said expanded cooled first portion is supplied as said bottom feed to said second absorbing means.
(b) said second portion is cooled to condense substantially all of said second portion and is thereafter expanded to said lower pressure whereby said second portion is further cooled;
(c) said expanded cooled second portion is supplied as said feed between said first and second absorbing means; and (d) said expanded cooled first portion is supplied as said bottom feed to said second absorbing means.
5. The process according to claim 4 wherein (a) said first portion is cooled sufficiently to partially condense said first portion;
(b) said partially condensed first portion is supplied to a separating means and is separated therein to provide a vapor stream and at least one liquid stream;
(c) said vapor stream is expanded to said lower pressure and is supplied as said first bottom feed to said second absorbing means; and (d) at least a portion of said at least one liquid stream is expanded to said lower pressure and is supplied as an additional bottom feed to said second absorbing means.
(b) said partially condensed first portion is supplied to a separating means and is separated therein to provide a vapor stream and at least one liquid stream;
(c) said vapor stream is expanded to said lower pressure and is supplied as said first bottom feed to said second absorbing means; and (d) at least a portion of said at least one liquid stream is expanded to said lower pressure and is supplied as an additional bottom feed to said second absorbing means.
6. The process according to claim 5 wherein (a) said second portion is cooled and is thereafter combined with at least a portion of said at least one liquid stream to form a combined stream;
(b) said combined stream is cooled to condense substantially all of said combined stream and is thereafter expanded to lower pressure whereby said combined stream is further cooled;
(c) said expanded cooled combined stream is supplied as said feel between said first and second absorbing means; and (d) any remaining portion of said at least one liquid stream is expanded to said lower pressure and is supplied as said additional bottom feed to said second absorbing means.
(b) said combined stream is cooled to condense substantially all of said combined stream and is thereafter expanded to lower pressure whereby said combined stream is further cooled;
(c) said expanded cooled combined stream is supplied as said feel between said first and second absorbing means; and (d) any remaining portion of said at least one liquid stream is expanded to said lower pressure and is supplied as said additional bottom feed to said second absorbing means.
7. The process according to claim 2 wherein (1) said heat and mass transfer means is arranged in upper and lower regions;
and (2) said expanded at least a portion of said at least one liquid stream is supplied to said processing assembly to enter between said upper and lower regions of said heat and mass transfer means.
and (2) said expanded at least a portion of said at least one liquid stream is supplied to said processing assembly to enter between said upper and lower regions of said heat and mass transfer means.
8. The process according to claim 3 wherein (1) said heat and mass transfer means is arranged in upper and lower regions;
and (2) said expanded any remaining portion of said at least one liquid stream is supplied to said processing assembly to enter between said upper and lower regions of said heat and mass transfer means.
and (2) said expanded any remaining portion of said at least one liquid stream is supplied to said processing assembly to enter between said upper and lower regions of said heat and mass transfer means.
9. The process according to claim 5 wherein (1) said heat and mass transfer means is arranged in upper and lower regions;
and (2) said expanded at least a portion of said at least one liquid stream is supplied to said processing assembly to enter between said upper and lower regions of said heat and mass transfer means.
and (2) said expanded at least a portion of said at least one liquid stream is supplied to said processing assembly to enter between said upper and lower regions of said heat and mass transfer means.
10. The process according to claim 6 wherein (1) said heat and mass transfer means is arranged in upper and lower regions;
and (2) said expanded any remaining portion of said at least one liquid stream is supplied to said processing assembly to enter between said upper and lower regions of said heat and mass transfer means.
and (2) said expanded any remaining portion of said at least one liquid stream is supplied to said processing assembly to enter between said upper and lower regions of said heat and mass transfer means.
11. The process according to claim 7, 8, 9, 10, 2, 3, 5, or 6 wherein said separating means is housed in said processing assembly.
12. The process according to claim 1 wherein (1) a gas collecting means is housed in said processing assembly;
(2) an additional heat and mass transfer means is included inside said gas collecting means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(3) said cooled gas stream is supplied to said gas collecting means and directed to said additional heat and mass transfer means to be further cooled by said external refrigeration medium; and (4) said further cooled gas stream is divided into said first and second streams.
(2) an additional heat and mass transfer means is included inside said gas collecting means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(3) said cooled gas stream is supplied to said gas collecting means and directed to said additional heat and mass transfer means to be further cooled by said external refrigeration medium; and (4) said further cooled gas stream is divided into said first and second streams.
13. The process according to claim 4 wherein (1) a gas collecting means is housed in said processing assembly;
(2) an additional heat and mass transfer means is included inside said gas collecting means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(3) said cooled first portion is supplied to said gas collecting means and directed to said additional heat and mass transfer means to be further cooled by said external refrigeration medium; and (4) said further cooled first portion is expanded to said lower pressure and is thereafter supplied as said bottom feed to said second absorbing means.
(2) an additional heat and mass transfer means is included inside said gas collecting means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(3) said cooled first portion is supplied to said gas collecting means and directed to said additional heat and mass transfer means to be further cooled by said external refrigeration medium; and (4) said further cooled first portion is expanded to said lower pressure and is thereafter supplied as said bottom feed to said second absorbing means.
14. The process according to claim 7, 8, 9, 10, 2, 3, 5, or 6 wherein (1) an additional heat and mass transfer means is included inside said separating means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(2) said vapor stream is directed to said additional heat and mass transfer means to be cooled by said external refrigeration medium to form additional condensate;
and (3) said condensate becomes a part of said at least one liquid stream separated therein.
(2) said vapor stream is directed to said additional heat and mass transfer means to be cooled by said external refrigeration medium to form additional condensate;
and (3) said condensate becomes a part of said at least one liquid stream separated therein.
15. The process according to claim 11 wherein (1) an additional heat and mass transfer means is included inside said separating means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(2) said vapor stream is directed to said additional heat and mass transfer means to be cooled by said external refrigeration medium to form additional condensate;
and (3) said condensate becomes a part of said at least one liquid stream separated therein.
(2) said vapor stream is directed to said additional heat and mass transfer means to be cooled by said external refrigeration medium to form additional condensate;
and (3) said condensate becomes a part of said at least one liquid stream separated therein.
16. The process according to claim 1, 7, 8, 9, 10, 12, 13, 2, 3, 4, 5, or 6 wherein said heat and mass transfer means includes one or more passes for an external heating medium to supplement the heating supplied by said second portion for said stripping of said more volatile components from said distillation liquid stream.
17. The process according to claim 11 wherein said heat and mass transfer means includes one or more passes for an external heating medium to supplement the heating supplied by said second portion for said stripping of said more volatile components from said distillation liquid stream.
18. The process according to claim 14 wherein said heat and mass transfer means includes one or more passes for an external heating medium to supplement the heating supplied by said second portion for said stripping of said more volatile components from said distillation liquid stream.
19. The process according to claim 15 wherein said heat and mass transfer means includes one or more passes for an external heating medium to supplement the heating supplied by said second portion for said stripping of said more volatile components from said distillation liquid stream.
20. An apparatus for the separation of a gas stream containing methane, C2 components, C3 components, and heavier hydrocarbon components into a volatile residue gas fraction and a relatively less volatile fraction containing a major portion of said C2 components, C3 components, and heavier hydrocarbon components or said C3 components and heavier hydrocarbon components comprising (I) first dividing means to divide said gas stream into first and second portions;
(2) heat exchange means connected to said first dividing means to receive said first portion and cool said first portion;
(3) heat and mass transfer means housed in a single equipment item processing assembly and connected to said first dividing means to receive said second portion and cool said second portion;
(4) combining means connected to said heat exchange means and said heat and mass transfer means to receive said cooled first portion and said cooled second portion and form a cooled gas stream;
(5) second dividing means connected to said combining means to receive said cooled gas stream and divide said cooled gas stream into first and second streams;
(6) said heat exchange means being further connected to said second dividing means to receive said first stream and cool said first stream sufficiently to substantially condense said first stream;
(7) first expansion means connected to said heat exchange means to receive said substantially condensed first stream and expand said substantially condensed first stream to lower pressure;
(8) first and second absorbing means housed in said processing assembly and connected to said first expansion means to receive said expanded cooled first stream as a feed thereto between said first and second absorbing means, said first absorbing means being located above said second absorbing means;
(9) second expansion means connected to said second dividing means to receive said second stream and expand said second stream to said lower pressure, said second expansion means being further connected to said second absorbing means to supply said expanded second stream as a bottom feed thereto;
(10) vapor collecting means housed in said processing assembly and connected to said first absorbing means to receive a distillation vapor stream from an upper region of said first absorbing means;
(11) said heat exchange means being further connected to said vapor collecting means to receive said distillation vapor stream and heat said distillation vapor stream, thereby to supply at least a portion of the cooling of steps (2) and (6);
(12) compressing means connected to said heat exchange means to receive said heated distillation vapor stream and compress said heated distillation vapor stream to higher pressure;
(13) cooling means connected to said compressing means to receive said compressed distillation vapor stream and cool said compressed distillation vapor stream;
(14) third dividing means connected to said cooling means to receive said cooled compressed distillation vapor stream and divide said cooled compressed distillation vapor stream into said volatile residue gas fraction and a compressed recycle stream;
(15) said heat exchange means being further connected to said third dividing means to receive said compressed recycle stream and cool said compressed recycle stream sufficiently to substantially condense said compressed recycle stream, thereby to supply at least a portion of the heating of step (11);
(16) third expansion means connected to said heat exchange means to receive said substantially condensed compressed recycle stream and expand said substantially condensed compressed recycle stream to said lower pressure, said third expansion means being further connected to said first absorbing means to supply said expanded recycle stream as a top feed thereto;
(17) liquid collecting means housed in said processing assembly and connected to said second absorbing means to receive a distillation liquid stream from a lower region of said second absorbing means;
(18) said heat and mass transfer means being further connected to said liquid collecting means to receive said distillation liquid stream and heat said distillation liquid stream, thereby to supply at least a portion of the cooling of step (3) while simultaneously stripping the more volatile components from said distillation liquid stream, and thereafter discharging said heated and stripped distillation liquid stream from said processing assembly as said relatively less volatile fraction; and (19) control means adapted to regulate the quantities and temperatures of said feed streams to said first and second absorbing means to maintain the temperature of said upper region of said first absorbing means at a temperature whereby the major portions of the components in said relatively less volatile fraction are recovered.
(2) heat exchange means connected to said first dividing means to receive said first portion and cool said first portion;
(3) heat and mass transfer means housed in a single equipment item processing assembly and connected to said first dividing means to receive said second portion and cool said second portion;
(4) combining means connected to said heat exchange means and said heat and mass transfer means to receive said cooled first portion and said cooled second portion and form a cooled gas stream;
(5) second dividing means connected to said combining means to receive said cooled gas stream and divide said cooled gas stream into first and second streams;
(6) said heat exchange means being further connected to said second dividing means to receive said first stream and cool said first stream sufficiently to substantially condense said first stream;
(7) first expansion means connected to said heat exchange means to receive said substantially condensed first stream and expand said substantially condensed first stream to lower pressure;
(8) first and second absorbing means housed in said processing assembly and connected to said first expansion means to receive said expanded cooled first stream as a feed thereto between said first and second absorbing means, said first absorbing means being located above said second absorbing means;
(9) second expansion means connected to said second dividing means to receive said second stream and expand said second stream to said lower pressure, said second expansion means being further connected to said second absorbing means to supply said expanded second stream as a bottom feed thereto;
(10) vapor collecting means housed in said processing assembly and connected to said first absorbing means to receive a distillation vapor stream from an upper region of said first absorbing means;
(11) said heat exchange means being further connected to said vapor collecting means to receive said distillation vapor stream and heat said distillation vapor stream, thereby to supply at least a portion of the cooling of steps (2) and (6);
(12) compressing means connected to said heat exchange means to receive said heated distillation vapor stream and compress said heated distillation vapor stream to higher pressure;
(13) cooling means connected to said compressing means to receive said compressed distillation vapor stream and cool said compressed distillation vapor stream;
(14) third dividing means connected to said cooling means to receive said cooled compressed distillation vapor stream and divide said cooled compressed distillation vapor stream into said volatile residue gas fraction and a compressed recycle stream;
(15) said heat exchange means being further connected to said third dividing means to receive said compressed recycle stream and cool said compressed recycle stream sufficiently to substantially condense said compressed recycle stream, thereby to supply at least a portion of the heating of step (11);
(16) third expansion means connected to said heat exchange means to receive said substantially condensed compressed recycle stream and expand said substantially condensed compressed recycle stream to said lower pressure, said third expansion means being further connected to said first absorbing means to supply said expanded recycle stream as a top feed thereto;
(17) liquid collecting means housed in said processing assembly and connected to said second absorbing means to receive a distillation liquid stream from a lower region of said second absorbing means;
(18) said heat and mass transfer means being further connected to said liquid collecting means to receive said distillation liquid stream and heat said distillation liquid stream, thereby to supply at least a portion of the cooling of step (3) while simultaneously stripping the more volatile components from said distillation liquid stream, and thereafter discharging said heated and stripped distillation liquid stream from said processing assembly as said relatively less volatile fraction; and (19) control means adapted to regulate the quantities and temperatures of said feed streams to said first and second absorbing means to maintain the temperature of said upper region of said first absorbing means at a temperature whereby the major portions of the components in said relatively less volatile fraction are recovered.
21. the apparatus according to claim 20 wherein (a) said combining means is connected to said heat exchange means and said heat and mass transfer means to receive said cooled first portion and said cooled second portion and form a partially condensed gas stream;
(b) a separating means is connected to said combining means to receive said partially condensed gas stream and separate said partially condensed gas stream into a vapor stream and at least one liquid stream;
(c) said second dividing means is connected to said separating means to receive said vapor stream and divide said vapor stream into said first and second streams;
and (d) a fourth expansion means is connected to said separating means to receive at least a portion of said at least one liquid stream and expand said at least one liquid stream to said lower pressure, said fourth expansion means being further connected to said second absorbing means to supply said expanded liquid stream as an additional bottom feed thereto.
(b) a separating means is connected to said combining means to receive said partially condensed gas stream and separate said partially condensed gas stream into a vapor stream and at least one liquid stream;
(c) said second dividing means is connected to said separating means to receive said vapor stream and divide said vapor stream into said first and second streams;
and (d) a fourth expansion means is connected to said separating means to receive at least a portion of said at least one liquid stream and expand said at least one liquid stream to said lower pressure, said fourth expansion means being further connected to said second absorbing means to supply said expanded liquid stream as an additional bottom feed thereto.
22. The apparatus according to claim 21 wherein (a) an additional combining means is connected to said second dividing means and said separating means to receive said first stream and at least a portion of said at least one liquid stream and form a combined stream;
(b) said heat exchange means is further connected to said additional combining means to receive said combined stream and cool said combined stream sufficiently to substantially condense it;
(c) said first expansion means is connected to said heat exchange means to receive said substantially condensed combined stream and expand said substantially condensed combined stream to lower pressure;
(d) said first and second absorbing means is connected to said first expansion means to receive said expanded cooled combined stream as said feed thereto between said first and second absorbing means; and (e) said fourth expansion means is connected to said separating means to receive any remaining portion of said at least one liquid stream and expand said any remaining portion of said at least one liquid stream to said lower pressure, said fourth expansion mean being further connected to said second absorbing means to supply said expanded liquid stream as said additional second bottom feed there.
(b) said heat exchange means is further connected to said additional combining means to receive said combined stream and cool said combined stream sufficiently to substantially condense it;
(c) said first expansion means is connected to said heat exchange means to receive said substantially condensed combined stream and expand said substantially condensed combined stream to lower pressure;
(d) said first and second absorbing means is connected to said first expansion means to receive said expanded cooled combined stream as said feed thereto between said first and second absorbing means; and (e) said fourth expansion means is connected to said separating means to receive any remaining portion of said at least one liquid stream and expand said any remaining portion of said at least one liquid stream to said lower pressure, said fourth expansion mean being further connected to said second absorbing means to supply said expanded liquid stream as said additional second bottom feed there.
23. The apparatus according to claim 20 wherein (a) said heat exchange means is further connected to said heat and mass transfer means to receive said cooled second portion, and further cool said cooled second portion sufficiently to substantially condense said cooled second portion;
(b) said first expansion means is connected to said heat exchange means to receive said substantially condensed second portion and expand said substantially condensed second portion to lower pressure;
(c) said first and second absorbing means is connected to said first expansion means to receive said expanded cooled second portion as said feed thereto between said first and second absorbing means; and (d) said second expansion means is connected to said heat exchange means to receive said cooled first portion and expand said cooled first portion to said lower pressure, said second expansion means being further connected to said second absorbing means to supply said expanded cooled first portion as said bottom feed thereto.
(b) said first expansion means is connected to said heat exchange means to receive said substantially condensed second portion and expand said substantially condensed second portion to lower pressure;
(c) said first and second absorbing means is connected to said first expansion means to receive said expanded cooled second portion as said feed thereto between said first and second absorbing means; and (d) said second expansion means is connected to said heat exchange means to receive said cooled first portion and expand said cooled first portion to said lower pressure, said second expansion means being further connected to said second absorbing means to supply said expanded cooled first portion as said bottom feed thereto.
24. The apparatus according to claim 23 wherein (a) said heat exchange means is connected to said first dividing means to receive said first portion and cool said first portion sufficiently to partially condense said first portion;
(b) a separating means is connected to said heat exchange means to receive said partially condensed first portion and to separate said partially condense first portion into a vapor stream and at least one liquid stream;
(c) said second expansion means is connected to said separating means to receive said vapor stream and expand said vapor stream to said lower pressure, said second expansion means being further connected to said second absorbing means to supply said expanded vapor stream as said first bottom feed thereto; and (d) a fourth expansion means is connected to said separating means to receive at least a portion of said at least one liquid stream and expand said at least one liquid stream to said lower pressure, said fourth expansion means being further connected to said second absorbing means to supply said expanded liquid stream as an additional bottom feed thereto.
(b) a separating means is connected to said heat exchange means to receive said partially condensed first portion and to separate said partially condense first portion into a vapor stream and at least one liquid stream;
(c) said second expansion means is connected to said separating means to receive said vapor stream and expand said vapor stream to said lower pressure, said second expansion means being further connected to said second absorbing means to supply said expanded vapor stream as said first bottom feed thereto; and (d) a fourth expansion means is connected to said separating means to receive at least a portion of said at least one liquid stream and expand said at least one liquid stream to said lower pressure, said fourth expansion means being further connected to said second absorbing means to supply said expanded liquid stream as an additional bottom feed thereto.
25. The apparatus according to claim 24 wherein (a) an additional combining means is connected to said heat and mass transfer means and said separating means to receive said cooled second portion and at least a portion of said at least one liquid stream and form a combined stream;
(b) said heat exchange means is further connected to said additional combining means to receive said combined stream and cool said combined stream sufficiently to substantially condense it;
(c) said first expansion means is connected to said heat exchange means to receive said substantially condensed combined stream and expand said substantially condensed combined stream to lower pressure;
(d) said first and second absorbing means is connected to said first expansion means to receive said expanded cooled combined stream as said feed thereto between said first second absorbing means; and (e) said fourth expansion means is connected to said separating means to receive any remaining portion of said at least one liquid stream and expand said any remaining portion of said at least one liquid stream to said lower pressure, said fourth expansion means being further connected to said second absorbing means to supply said expanded liquid stream as said additional bottom feed thereto.
(b) said heat exchange means is further connected to said additional combining means to receive said combined stream and cool said combined stream sufficiently to substantially condense it;
(c) said first expansion means is connected to said heat exchange means to receive said substantially condensed combined stream and expand said substantially condensed combined stream to lower pressure;
(d) said first and second absorbing means is connected to said first expansion means to receive said expanded cooled combined stream as said feed thereto between said first second absorbing means; and (e) said fourth expansion means is connected to said separating means to receive any remaining portion of said at least one liquid stream and expand said any remaining portion of said at least one liquid stream to said lower pressure, said fourth expansion means being further connected to said second absorbing means to supply said expanded liquid stream as said additional bottom feed thereto.
26. The apparatus according to claim 21 wherein (1) said heat and mass transfer means is arranged in upper and lower regions;
and (2) said processing assembly is connected to said third expansion means to receive said expanded liquid stream and direct said expanded liquid stream between said upper and lower regions of said heat and mass transfer means.
and (2) said processing assembly is connected to said third expansion means to receive said expanded liquid stream and direct said expanded liquid stream between said upper and lower regions of said heat and mass transfer means.
27. The apparatus according to claim 22 wherein (1) said heat and mass transfer means is arranged in upper and lower regions;
and (2) said processing assembly is connected to said third expansion means to receive said expanded liquid stream and direct said expanded liquid stream between said upper and lower regions of said heat and mass transfer means.
and (2) said processing assembly is connected to said third expansion means to receive said expanded liquid stream and direct said expanded liquid stream between said upper and lower regions of said heat and mass transfer means.
28. The apparatus according to claim 24 wherein (1) said heat and mass transfer means is arranged in upper and lower regions;
and (2) said processing assembly is connected to said third expansion means to receive said expanded liquid stream and direct said expanded liquid stream between said upper and lower regions of said heat and mass transfer means.
and (2) said processing assembly is connected to said third expansion means to receive said expanded liquid stream and direct said expanded liquid stream between said upper and lower regions of said heat and mass transfer means.
29. The apparatus according to claim 25 wherein (1) said heat and mass transfer means is arranged in upper and lower regions;
and (2) said processing assembly is connected to said third expansion means to receive said expanded liquid stream and direct said expanded liquid stream between said upper and lower regions of said heat and mass transfer means.
and (2) said processing assembly is connected to said third expansion means to receive said expanded liquid stream and direct said expanded liquid stream between said upper and lower regions of said heat and mass transfer means.
30. The apparatus according to claims 21, 22, 24, 25, 26, 27, 28, or 29 wherein said separating means is housed in said processing assembly.
31. The apparatus according to claim 20 wherein (1) a gas collecting means is housed in said processing assembly;
(2) an additional heat and mass transfer means is included inside said gas collecting means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(3) said gas collecting means is connected to said combining means to receive said cooled gas stream and direct said cooled gas stream to said additional heat and mass transfer means to be further cooled by said external refrigeration medium; and (4) said second dividing means is adapted to be connected to said gas collecting means to receive said further cooled gas stream and divide said further cooled gas stream into said first and second streams.
(2) an additional heat and mass transfer means is included inside said gas collecting means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(3) said gas collecting means is connected to said combining means to receive said cooled gas stream and direct said cooled gas stream to said additional heat and mass transfer means to be further cooled by said external refrigeration medium; and (4) said second dividing means is adapted to be connected to said gas collecting means to receive said further cooled gas stream and divide said further cooled gas stream into said first and second streams.
32. The apparatus according to claim 23 wherein (1) a gas collecting means is housed in said processing assembly;
(2) an additional heat and mass transfer means is included inside said gas collecting means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(3) said gas collecting means is connected to said heat exchange means to receive said cooled first portion and direct said cooled first portion to said additional heat and mass transfer means to be further cooled by said external refrigeration medium; and (4) said second expansion means is adapted to be connected to said gas collecting means to receive said further cooled first portion and expand said further cooled first portion to said lower pressure, said second expansion means being further connected to said second absorbing means to supply said expanded further cooled first portion as said bottom feed thereto.
(2) an additional heat and mass transfer means is included inside said gas collecting means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(3) said gas collecting means is connected to said heat exchange means to receive said cooled first portion and direct said cooled first portion to said additional heat and mass transfer means to be further cooled by said external refrigeration medium; and (4) said second expansion means is adapted to be connected to said gas collecting means to receive said further cooled first portion and expand said further cooled first portion to said lower pressure, said second expansion means being further connected to said second absorbing means to supply said expanded further cooled first portion as said bottom feed thereto.
33. The apparatus according to claims 21, 22, 24, 25, 26, 27, 28, or 29 wherein (1) an additional heat and mass transfer means is included inside said separating means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(2) said vapor stream is directed to said additional heat and mass transfer means to be cooled by said external refrigeration medium to form additional condensate;
and (3) said condensate becomes a part of said at least one liquid stream separated therein.
(2) said vapor stream is directed to said additional heat and mass transfer means to be cooled by said external refrigeration medium to form additional condensate;
and (3) said condensate becomes a part of said at least one liquid stream separated therein.
34. The apparatus according to claim 30 wherein (1) an additional heat and mass transfer means is included inside said separating means, said additional heat and mass transfer means including one or more passes for an external refrigeration medium;
(2) said vapor stream is directed to said additional heat and mass transfer means to be cooled by said external refrigeration medium to form additional condensate;
and (3) said condensate becomes a part of said at least one liquid stream separated therein.
(2) said vapor stream is directed to said additional heat and mass transfer means to be cooled by said external refrigeration medium to form additional condensate;
and (3) said condensate becomes a part of said at least one liquid stream separated therein.
35. The apparatus according to claim 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 31, or 32 wherein said heat and mass transfer means includes one or more passes for an external heating medium to supplement the heating supplied by said second portion for said stripping of said more volatile components from said distillation liquid stream.
36. The apparatus according to claim 30 wherein said heat and mass transfer means includes one or more passes for an external heating medium to supplement the heating supplied by said second portion for said stripping of said more volatile components from said distillation liquid stream.
37. The apparatus according to claim 33 wherein said heat and mass transfer means includes one or more passes for an external heating medium to supplement the heating supplied by said second portion for said stripping of said more volatile components from said distillation liquid stream.
38. The apparatus according to claim 34 wherein said heat and mass transfer means includes one or more passes for an external heating medium to supplement the heating supplied by said second portion for said stripping of said more volatile components from said distillation liquid stream.
Applications Claiming Priority (23)
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USPCT/US2010/029331 | 2010-03-31 | ||
US12/750,862 | 2010-03-31 | ||
US12/750,862 US8881549B2 (en) | 2009-02-17 | 2010-03-31 | Hydrocarbon gas processing |
PCT/US2010/029331 WO2010144172A1 (en) | 2009-06-11 | 2010-03-31 | Hydrocarbon gas processing |
US12/772,472 | 2010-05-03 | ||
USPCT/US2010/033374 | 2010-05-03 | ||
PCT/US2010/033374 WO2010144186A1 (en) | 2009-06-11 | 2010-05-03 | Hydrocarbon gas processing |
US12/772,472 US9933207B2 (en) | 2009-02-17 | 2010-05-03 | Hydrocarbon gas processing |
USPCT/US2010/035121 | 2010-05-17 | ||
PCT/US2010/035121 WO2010144217A1 (en) | 2009-06-11 | 2010-05-17 | Hydrocarbon gas processing |
US12/781,259 | 2010-05-17 | ||
US12/781,259 US9939195B2 (en) | 2009-02-17 | 2010-05-17 | Hydrocarbon gas processing including a single equipment item processing assembly |
US13/048,315 US9052136B2 (en) | 2010-03-31 | 2011-03-15 | Hydrocarbon gas processing |
US13/048,315 | 2011-03-15 | ||
USPCT/US2011/028872 | 2011-03-17 | ||
PCT/US2011/028872 WO2011123253A1 (en) | 2010-03-31 | 2011-03-17 | Hydrocarbon gas processing |
USPCT/US2011/029034 | 2011-03-18 | ||
US13/051,682 | 2011-03-18 | ||
PCT/US2011/029034 WO2011126710A1 (en) | 2010-03-31 | 2011-03-18 | Hydrocarbon gas processing |
US13/051,682 US9074814B2 (en) | 2010-03-31 | 2011-03-18 | Hydrocarbon gas processing |
US13/052,348 | 2011-03-21 | ||
PCT/US2011/029234 WO2011123276A1 (en) | 2009-02-17 | 2011-03-21 | Hydrocarbon gas processing |
US13/052,348 US9052137B2 (en) | 2009-02-17 | 2011-03-21 | Hydrocarbon gas processing |
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CN (1) | CN102695934B (en) |
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US9783470B2 (en) * | 2013-09-11 | 2017-10-10 | Ortloff Engineers, Ltd. | Hydrocarbon gas processing |
CN108507277A (en) * | 2018-04-28 | 2018-09-07 | 中国石油工程建设有限公司 | A kind of the cold comprehensive utilization device and method of natural gas ethane recovery |
CA3132386A1 (en) * | 2019-03-11 | 2020-09-17 | Uop Llc | Hydrocarbon gas processing |
CN111763131A (en) * | 2019-04-02 | 2020-10-13 | 天津中油科远石油工程有限责任公司 | Method and device for producing ethane by cold dry gas reflux |
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US5568737A (en) * | 1994-11-10 | 1996-10-29 | Elcor Corporation | Hydrocarbon gas processing |
US5675054A (en) * | 1995-07-17 | 1997-10-07 | Manley; David | Low cost thermal coupling in ethylene recovery |
US5685170A (en) * | 1995-11-03 | 1997-11-11 | Mcdermott Engineers & Constructors (Canada) Ltd. | Propane recovery process |
US7310971B2 (en) * | 2004-10-25 | 2007-12-25 | Conocophillips Company | LNG system employing optimized heat exchangers to provide liquid reflux stream |
US6516631B1 (en) * | 2001-08-10 | 2003-02-11 | Mark A. Trebble | Hydrocarbon gas processing |
US6694775B1 (en) * | 2002-12-12 | 2004-02-24 | Air Products And Chemicals, Inc. | Process and apparatus for the recovery of krypton and/or xenon |
US7484385B2 (en) * | 2003-01-16 | 2009-02-03 | Lummus Technology Inc. | Multiple reflux stream hydrocarbon recovery process |
US9933207B2 (en) * | 2009-02-17 | 2018-04-03 | Ortloff Engineers, Ltd. | Hydrocarbon gas processing |
AR076506A1 (en) * | 2009-06-11 | 2011-06-15 | Sme Products Lp | HYDROCARBON GAS PROCESSING |
EA022763B1 (en) * | 2009-06-11 | 2016-02-29 | Ортлофф Инджинирс, Лтд. | Hydrocarbon gas processing |
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MY160876A (en) | 2017-03-31 |
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