CN104419466B - A kind of oil refinery dry gas recovery system and dry-gas recovery method - Google Patents

A kind of oil refinery dry gas recovery system and dry-gas recovery method Download PDF

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CN104419466B
CN104419466B CN201310409583.9A CN201310409583A CN104419466B CN 104419466 B CN104419466 B CN 104419466B CN 201310409583 A CN201310409583 A CN 201310409583A CN 104419466 B CN104419466 B CN 104419466B
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tower
gas
absorption tower
oil refinery
absorption
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CN104419466A (en
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李东风
罗淑娟
刘智信
程建民
廖丽华
过良
李琰
王婧
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Sinopec Beijing Research Institute of Chemical Industry
China Petroleum and Chemical Corp
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Sinopec Beijing Research Institute of Chemical Industry
China Petroleum and Chemical Corp
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G70/00Working-up undefined normally gaseous mixtures obtained by processes covered by groups C10G9/00, C10G11/00, C10G15/00, C10G47/00, C10G51/00
    • C10G70/04Working-up undefined normally gaseous mixtures obtained by processes covered by groups C10G9/00, C10G11/00, C10G15/00, C10G47/00, C10G51/00 by physical processes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G70/00Working-up undefined normally gaseous mixtures obtained by processes covered by groups C10G9/00, C10G11/00, C10G15/00, C10G47/00, C10G51/00
    • C10G70/04Working-up undefined normally gaseous mixtures obtained by processes covered by groups C10G9/00, C10G11/00, C10G15/00, C10G47/00, C10G51/00 by physical processes
    • C10G70/06Working-up undefined normally gaseous mixtures obtained by processes covered by groups C10G9/00, C10G11/00, C10G15/00, C10G47/00, C10G51/00 by physical processes by gas-liquid contact

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

The invention discloses a kind of oil refinery dry gas recovery system and method.Described system includes: compressor, absorption tower, reabsorber, Analytic Tower, cooler, choke valve and flash tank;Compressor connects absorption tower after connecting heat exchanger, and top, absorption tower connects reabsorber, connects Analytic Tower bottom absorption tower, and Analytic Tower top is sequentially connected with cooler, choke valve and flash tank, and flash drum overhead connects suction port of compressor.Method includes: oil refinery dry gas is compressed, cool down, absorb, resolve, liquefy after obtain rich carbon two product.The inventive method equipment is few, and energy consumption is low, and flow process is simple, and the response rate is high, and product is easily stored and transports.

Description

A kind of oil refinery dry gas recovery system and dry-gas recovery method
Technical field
The present invention relates to oil refinery dry gas process field, furtherly, relate to a kind of dry-gas recovery system and do Gas recovery method.
Background technology
Oil refinery dry gas is mainly derived from the secondary processing process of crude oil, such as catalytic cracking, thermal cracking, delay coke Change, be hydrocracked.In general catalysis drying gas, ethylene contents is higher, and in coking dry gas, ethane content is higher, 15%~about 25%, additionally, possibly together with alkene alkane such as propylene, propane, butane in oil refinery dry gas.At present, Major part refinery of China will burn as fuel gas by oil refinery dry gas, and value is relatively low, and causes greatly The wasting of resources and environmental pollution.
Ethane is ideal cracking stock, and in steam-cracking process, sizable Partial Conversion becomes Ethylene.If by the ethane recovery in oil refinery dry gas, being sent to ethylene producing device, not only take full advantage of refinery Tail gas resource, and reduce cracking stock cost, embody Integrated Refinery And Petrochemical advantage.But, for pure From the point of view of Refining of Petroleum enterprise, owing to without ethylene producing device, how the rich ethane gas of recovery transports and storage is anxious The problem needing to solve.
The method reclaiming ethylene at present from oil refinery dry gas mainly has separation by deep refrigeration, middle cold oil absorption process, network Closing partition method, pressure swing adsorption method etc., various methods differ from one another.Separation by deep refrigeration technical maturity, ethylene returns Yield is high, but investment is big, higher for dilute ethylene recovery energy consumption;Separation by Complexation method, Recovery rate of ethylene is higher, But requiring the impurity in raw material strict, pretreatment costly, needs special complexes absorption;Transformation Absorption method is simple to operate, and energy consumption is relatively low, but product purity is low, and Recovery rate of ethylene is low, and floor space is big.
Middle cold oil absorption process separates gas mainly by absorbent to the different solubility of component each in gas Mixture, typically absorbs the heavy constituent of C2 and more than C2, isolates methane, hydrogen etc. first with absorbent Incoagulable gas, then by each component in rectification method separate absorbent agent.The method has small scale, adaptability The feature such as by force, investment cost is low.
CN1640992 proposes a kind of refrigeration oil absorption process with the self-produced stable light hydrocarbon of device as absorbent, Be applicable to recovered liquid activating QI from associated gas or natural gas, and C3 yield requires higher recovery process. Use the absorption process of this refrigeration oil, less absorbent can be used, it is thus achieved that higher light hydrocarbon recovery rate, and Technique is simple, and energy consumption is relatively low, better economic benefit.But the method is only applicable to from associated gas or natural Recovered liquid activating QI in gas, can not reclaim C2 fraction, it is impossible to for the recovery of plant catalytic dry gas.
US5502971 discloses a kind of low-pressure low-temperature technique reclaiming C2 and more heavy hydrocarbons, it is adaptable to refinery The recovery of dry gas.This technique eliminates traditional high pressure scheme, changes and uses low-voltage technology, so reclaims temperature Degree is maintained on the temperature that nitric acid resin generates, it is to avoid dangerous Potential feasibility, also simultaneously Higher olefin yields can be kept.The process employs low pressure scheme, temperature is low reaches-100 DEG C, belongs to deep cooling The one of separating technology, investment is relatively big, and energy consumption is higher.
US6308532 proposes a kind of recovery ethylene and technique of propylene from oil refinery dry gas, and this technique includes Extracting C3 out from absorbing tower reactor, part tower bottoms phase materials is also recycled to tower top, thus protects by C4, C5, C6 liquid The cryogenic temperature holding overhead condenser is not less than-95 DEG C, simultaneously rich in propylene or ethylene-propylene district in absorption tower Gas phase side line is extracted in territory out.Will not with holding tower top temperature although part kettle material is recycled to tower top by this technique In too low, but tower top temperature is the lowest reaches-95 DEG C, still falls within the one of deep cooling process for separating, therefore invests relatively big, Energy consumption is higher.
CN101063048A discloses a kind of method of cold oil absorption process separating plant catalytic dry gas in using, This technique is by compressing, remove sour gas, being dried and purification, absorption, desorbing, cold recovery and rough segmentation etc. Step forms, and has absorbent with low cost, loses the advantages such as low.But, the method absorbent circulating load Greatly, equipment size is big, and process CIMS is complicated, and product purity is the highest.Additionally, this technique reclaims products obtained therefrom For gas phase C-2-fraction and ethane, pipeline can only be used to carry, cause the suitability of the program by the relatively day of one's doom System.
In sum, the existence investment of existing oil refinery dry gas recycling technique is big, energy consumption is high, the suitability is subject to The problems such as limit.
Summary of the invention
In order to solve in prior art, the existence investment of existing oil refinery dry gas recycling technique is big, energy consumption is high, technique The problems such as the suitability is limited, the invention provides a kind of oil refinery dry gas recovery system and dry-gas recovery method.This Invention reclaims with absorbent carbon two component in dry gas, keeps absorbing temperature at about 15 degree, absorption tower Top gas is reclaimed by resorbent mode, absorbs tower bottoms and obtains carbon two concentrated gas by desorbing, then carries out cold But liquefy.The inventive method equipment is few, and energy consumption is low, and flow process is simple, and the response rate is high, product easily stored and Transport.
An object of the present invention is to provide a kind of oil refinery dry gas recovery system.
Including: compressor, absorption tower, reabsorber, desorber, cooler, choke valve and flash tank;
Compressor connects absorption tower after connecting heat exchanger, and top, absorption tower connects reabsorber, connects bottom absorption tower Connecing Analytic Tower, desorber top is sequentially connected with cooler, choke valve and flash tank, and flash drum overhead connects pressure Contracting machine entrance.
Described absorption tower arranges absorption tower tower reactor reboiler;Analytic Tower arranges Analytic Tower tower reactor reboiler.
Cooler preferred propylene cooler.
The two of the purpose of the present invention are to provide a kind of dry-gas recovery method.
Including: oil refinery dry gas is compressed, cool down, absorb, desorbing, obtain rich carbon two product after liquefaction.
Specifically include following steps:
1) the compressed pressure of oil refinery dry gas brings up to 3.0~5.0MPa;It is cooled to 5~15 DEG C and enters absorption tower;
2) absorbent sprays into from top, absorption tower, absorbs C2 fraction and more heavy component in oil refinery dry gas;Absorb Desorber is delivered in the tower reactor logistics of tower, and tower top unabsorbed gases logistics enters reabsorber;
3) re-absorption agent enters from reabsorber jacking, absorbs the absorbent that is carried over and is not got off by absorption C2 component;
4) the C2 concentrated gas that desorber tower top is recycled, the lean solvent that tower reactor obtains after cooling, Return to top, absorption tower;
5) rich carbon two product is obtained after the further cooling liquid of C2 concentrated gas that desorber tower top obtains;
Described absorbent is the C3 fraction containing propane, containing normal butane, the C-4-fraction of iso-butane, or Containing pentane, the C5 fraction of isopentane;It is preferably containing normal butane, the C-4-fraction of iso-butane;
Described re-absorption agent is the stable gasoline component of gasoline, heavy naphtha or Aromatic raffinate, preferably refinery.
Concrete technical scheme is as follows:
The oil refinery dry gas of the present invention recycles technique, comprises the following steps:
1) compression: will from refinery catalytic cracking, thermal cracking, delayed coking, the technical process such as be hydrocracked The dry gas pressure produced brings up to 3.0~5.0MPa;
2) cooling: the dry gas after the compression obtain described step 1) is cooled to 5~15 DEG C;
3) absorb: absorbent sprays into from top, absorption tower, absorb C2 fraction and more heavy component in oil refinery dry gas; The tower reactor logistics on main absorption tower is delivered to desorber and is processed;Tower top unabsorbed gases logistics enters reabsorber Reclaim absorbent therein;
4) desorbing: from absorption tower tower reactor logistics enter desorber, the C2 concentrated gas that tower top is recycled, The lean solvent that tower reactor obtains, after cooling, returns to top, absorption tower and recycles as absorbent.
5) liquefaction: utilize the C2 concentrated gas cooling liquid that desorber tower top is obtained by propylene refrigerant, then will Its throttling expansion is to normal pressure so that C2 concentrated gas temperature reduces further, the logistics after throttling through flash distillation, After gas-liquid separation, liquid phase is sent to tank field as product.
In compression step, oil refinery dry gas is it is generally required to improve pressure, preferably pressure step by step and bring up to 3.0~5.0MPa, to the hop count compressed, there is no particular limitation, it is preferred to use three sections of compressions;
In cooling step, preferably oil refinery dry gas being cooled to 5~15 DEG C, institute's chilling requirement is by propylene refrigeration compressor Machine provides corresponding cold.
In absorption step, the absorbent consumption on described absorption tower not particularly requirement, people in the art Member can determine according to the general knowledge of prior art.
Described absorption tower Optimization Theory plate number is 25~60, and operation pressure is 3.0~6.0MPa, and tower top temperature is 10 DEG C~40 DEG C.
The gaseous stream of described absorption tower tower top enters reabsorber, and re-absorption agent enters from tower top, absorbs quilt The absorbent taken out of and carbon two component do not got off by absorption;Top gaseous phase is directly discharged into fuel gas pipe network, tower Still liquid phase extraction is sent to outside battery limit (BL);
In desorption procedure, there is pressure reduction owing to carrying out the pressure of the tower reactor logistics on autonomous absorption tower with desorber, Therefore pressure reduction is relied on can to enter desorber.
In the method for the invention, the absorbent after the desorbing that desorber tower reactor obtains returns after cooling step by step Absorption tower recycles.
In the present invention, absorbent can enter reabsorber with main absorption top gaseous phase, it is therefore preferable that solving Inhale tower reactor introduce one absorbent as supplement, with absorptive tower absorbent consumption main in guarantee system.
The number of theoretical plate of the most described desorber is 20~60, and operation pressure is 1.0~4.0MPa.
In step (5), the desorbing tower top carbon two further cooling liquid of concentrated gas, the most first use 0 DEG C and -40 DEG C of level propylene refrigerants cool down, then by being throttled to normal pressure so that C2 concentrated gas cools down further, Gas phase after throttling returns compression unit circulation, and liquid phase is as product extraction.
C2 concentrated gas mainly contains the ethylene of 0-40%wt, the ethane of 25-80%wt and the third of 0-20%wt Alkene.
In the present invention, absorption tower tower reactor arranges reboiler, to ensure to absorb the light component such as tower reactor methane, hydrogen Drop to set below requirement.Wherein to add thermal medium permissible for absorption tower tower reactor reboiler and desorber tower reactor reboiler Use low-pressure steam, it would however also be possible to employ deep fat, preferably deep fat heating, refinery's affluence heat can be made full use of, Also process energy consumption can be reduced.
The method of the present invention can also include removing sour gas step, before entering absorption tower or from solution Carry out de-Sour gas disposal after analysis overhead extraction gas phase, amine can be used to wash, it would however also be possible to employ alkali cleaning takes off Except sour gas, remove sour gas, preferably alkali wash the most after desorption and take off sour gas.
The method of the present invention can also include drying steps.It is dried before can being arranged on entrance absorption tower, also Can be arranged in step (5) liquefaction process, preferably be dried in concentrated gas liquefaction process: propylene system Cold compressor can provide the cryogen of two ranks, 0 DEG C and-40 DEG C.Concentrated gas liquefaction process is dried, It is dried after referring to be cooled down by concentrated gas with 0 DEG C of propylene refrigerant.
The oil refinery dry gas Application way of the present invention has the following characteristics that
(1) product is liquid phase C2 concentrated gas, it is easy to stores and transports so that the scope of application of this technique is more Wide.
(2) carbon two concentration gas liquefaction process uses propylene refrigerant and choke valve to complete, and not only saves energy consumption, And decreasing ethylene refrigeration compressor complete equipment, investment substantially reduces.
(3) present invention uses refinery's low-grade deep fat heating, and energy consumption is substantially reduced.
(4) cold that gas phase C2 concentration gas and oil refinery dry gas all can use propylene refrigeration compressor to provide enters Row cooling, a set of refrigeration system not only liquefies final products, can be again that other users of technique provide cold, Capacity utilization maximizes, and reduces energy consumption and investment.
(5) absorbent selectivity is preferable, and each absorbent assimilation effect is the most more satisfactory, can be according to not With producer's situation, select optimum absorbent.
Accompanying drawing explanation
Fig. 1 is the oil refinery dry gas recovery system schematic diagram of the present invention
Description of reference numerals:
1 compressor;2 heat exchangers;3 absorption towers;4 desorbers;5 reabsorbers;6 coolers;7 throttlings Valve;8 flash tanks;9 oil refinery dry gas;10 supplement absorbent;11 re-absorption agent;12 rich carbon two products;13 Fuel gas;14 rich re-absorption agent;15 heavy constituents
Detailed description of the invention
Below in conjunction with embodiment, further illustrate the present invention.
Embodiment:
As it is shown in figure 1, a kind of oil refinery dry gas recovery system.Including: compressor 1, absorption tower 3, re-absorption Tower 5, Analytic Tower 4, cooler 6, choke valve 7 and flash tank 8;Compressor 1 connects after connecting heat exchanger 2 Connecing absorption tower 3, top, absorption tower 3 connects reabsorber 5, connects Analytic Tower 4, resolve bottom absorption tower 3 Tower 4 top is sequentially connected with cooler 6, choke valve 7 and flash tank 8, and flash tank 8 top connects compressor 1 Entrance.Described absorption tower 3 arranges absorption tower tower reactor reboiler;Analytic Tower 4 arranges Analytic Tower tower reactor reboiler.
Certain oil refinery dry gas composition is as shown in table 1,
Table 1
Composition Mol% Kmol/h
H2 26.18 371.06
N2 9.48 134.37
O2 0.00 0.00
CO 0.00 0.00
CO2 1.37 19.45
H2S 0.00 0.00
CH4 37.75 535.15
C2H6 14.76 209.18
C2H4 2.57 36.42
C3H8 4.60 65.17
C3H6 0.36 5.07
Iso-butane 1.97 27.91
Normal butane 0.05 0.72
Isobutene. 0.02 0.32
1-butylene 0.01 0.10
Cis-2-butene 0.01 0.08
Trans-2-butene 0.01 0.16
1,3-butadiene 0.00 0.00
Pentane 0.36 5.07
Isopentane 0.00 0.00
Hexane 0.15 2.14
Water 0.37 5.22
Oil refinery dry gas supplied materials is 26700kg/h, and after selecting ether, carbon four is as absorbent, reclaims in oil refinery dry gas Ethane and ethylene.
Oil refinery dry gas reclaims and comprises the following steps:
(1) compression: oil refinery dry gas is sent to compressibility, compresses through two-stage nitration, and pressure is increased to 3.9MPa, It is cooled to 14 DEG C and enters absorption tower;
(2) absorb: the number of theoretical plate on absorption tower is 33, and operation pressure is 3.8MPag, 20 DEG C of j of tower top temperature Lyosoption used is carbon four after ether, and solvent enters in tower from absorbing tower jacking, and dry gas enters from the 19th block of column plate Enter.C2 and heavy constituent thereof in dry gas are got off by solvent absorption, and from tower reactor extraction, tower top is methane, hydrogen Etc. light component, and it is entrained with a small amount of absorbent.
(3) desorbing: the number of theoretical plate of desorber is 40, operation pressure is 2.1MPag.Absorb in dry gas The rich solvent of the components such as C2 enters desorber from the 15th block of column plate, the C2 concentrated gas after desorbing from overhead extraction, Lean solvent is cooled to 13 DEG C after stage-by-stage heat exchange and returns absorption tower recycling.
(4) re-absorption: absorb tower top unabsorbed gases and enter reabsorber, the theoretical plate of reabsorber Number is 20, and operation pressure is 3.5MPag.Re-absorption agent uses stable gasoline, enters reabsorber from tower top, Absorbing carbon two component and carbon four absorbent, reabsorber tower reactor is rich gasoline, as the extraction of one of product, send Toward refinery's absorbing-stabilizing system.Reabsorber top gaseous phase is sent to fuel gas pipe network.
(5) liquefaction: the C2 concentrated gas propylene refrigerant of desorber overhead extraction liquefies, and then passes through Being throttled to normal pressure, make carbon two product temperature reduce further, the liquid phase after throttling is as product extraction, gas phase Return compression unit.
Obtained C-2-fraction forms such as table 2.
Table 2 carbon two product forms
Composition Wt% Kg/h
Methane 0.17 16.84
Ethane 59.93 6034.79
Ethylene 5.57 561.09
Propane 24.64 2481.17
Propylene 1.95 196.31
Carbon four 7.74 779.66
In the present embodiment, carbon two response rate is 91%.

Claims (10)

1. an oil refinery dry gas recovery system, it is characterised in that described system includes:
Compressor, absorption tower, reabsorber, Analytic Tower, cooler, choke valve and flash tank;
Compressor connects absorption tower after connecting heat exchanger, and top, absorption tower connects reabsorber, connects Analytic Tower bottom absorption tower, and Analytic Tower top is sequentially connected with cooler, choke valve and flash tank, and flash drum overhead connects suction port of compressor;
Described cooler uses propylene cooler.
2. oil refinery dry gas recovery system as claimed in claim 1, it is characterised in that:
Described absorption tower arranges absorption tower tower reactor reboiler;Desorber arranges desorber tower reactor reboiler.
3. oil refinery dry gas recovery system as claimed in claim 2, it is characterised in that:
Reboiler uses refinery's deep fat heating.
4. the dry-gas recovery method of the oil refinery dry gas recovery system used as described in one of claims 1 to 3, it is characterised in that described method includes:
Oil refinery dry gas is compressed, cool down, absorb, desorbing, obtain rich carbon two product after liquefaction.
5. dry-gas recovery method as claimed in claim 4, it is characterised in that described method includes:
1) the compressed pressure of oil refinery dry gas brings up to 3.0~5.0MPa;It is cooled to 5~15 DEG C and enters absorption tower;
2) absorbent sprays into from top, absorption tower, absorbs C2 fraction and more heavy component in oil refinery dry gas;Desorber is delivered in the tower reactor logistics on absorption tower, and tower top unabsorbed gases logistics enters reabsorber;
3) re-absorption agent enters from reabsorber jacking, absorbs the absorbent being carried over and the C2 component do not got off by absorption;
4) the C2 concentrated gas that desorber tower top is recycled, the lean solvent that tower reactor obtains, after cooling, returns to top, absorption tower;
5) rich carbon two product is obtained after the cooled liquefaction of C2 concentrated gas that desorber tower top obtains;
Described absorbent is the C3 fraction containing propane, containing normal butane, the C-4-fraction of iso-butane, or containing pentane, the C5 fraction of isopentane;
Described re-absorption agent is gasoline, heavy naphtha or Aromatic raffinate.
6. dry-gas recovery method as claimed in claim 5, it is characterised in that:
Described absorbent is containing normal butane, the C-4-fraction of iso-butane;
Described re-absorption agent is gasoline.
7. dry-gas recovery method as claimed in claim 5, it is characterised in that:
The number of theoretical plate on described absorption tower is 25~60, and operation pressure is 3.0~6.0MPa, and tower top temperature is 10 DEG C~40 DEG C;
The number of theoretical plate of described desorber is 20-60, and operation pressure is 1.0-4.0MPa,
The number of theoretical plate of described reabsorber is 10-50, and operation pressure is 1.0-4.0MPa.
8. dry-gas recovery method as claimed in claim 5, it is characterised in that:
Oil refinery dry gas is entering before absorption tower or analytically carry out de-Sour gas disposal after overhead extraction gas phase;
It is dried when oil refinery dry gas is before entering absorption tower or in C2 concentrated gas cooling liquid.
9. dry-gas recovery method as claimed in claim 5, it is characterised in that:
Step 5) in cooling be first to be respectively adopted 0 DEG C and the cooling of-40 DEG C of level propylene refrigerants, the most again by C2 concentrated gas throttling expansion to normal pressure so that C2 concentrated gas temperature reduces further.
10. the dry-gas recovery method as described in one of claim 5-9, it is characterised in that:
Containing the ethylene of 0-40wt%, the ethane of 25-80wt% and the propylene of 0-20wt% in C2 concentrated gas.
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