CN104557385A - Refinery mixed dry gas recovery system and recovery method - Google Patents
Refinery mixed dry gas recovery system and recovery method Download PDFInfo
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Abstract
The invention discloses a refinery mixed dry gas recovery system and a recovery method. The system comprises an unsaturated dry gas recovery device, a saturated dry gas recovery device and a reabsorber, wherein each of the unsaturated dry gas recovery device and the saturated dry gas recovery device comprises a compressor, an absorption tower and a desorption tower; the compressors are connected with the absorption towers, reactors of the absorption towers are connected with the desorption towers, and reactors of the desorption towers are connected with the upper parts of the absorption towers; the tops of the absorption towers of the unsaturated dry gas recovery device and the saturated dry gas recovery device are respectively connected with the reabsorber. Refinery dry gas consists of saturated dry gas and unsaturated dry gas which are respectively recovered by an absorption-desorption method, and a saturated C2 concentrated gas product and an unsaturated C2 concentrated gas product are obtained from the tower tops of the desorption towers and are respectively delivered to an ethylene unit cracking furnace and an alkali scrubbing tower. A gas phase of the tower top of each absorption tower is delivered to the reabsorber for unified treatment in a centralized manner. The method disclosed by the invention is high in recovery ratio and low in energy consumption, and the operation of an ethylene unit is hardly affected.
Description
Technical field
The present invention relates to dry-gas recovery field, furtherly, relate to a kind of refinery mixing dry gas recovery system and recovery method.
Background technology
Oil refinery dry gas is mainly derived from the secondary processing process of crude oil, as catalytic cracking, thermally splitting, delayed coking, hydrocracking etc.At present, major part refinery of China will burn as fuel gas by oil refinery dry gas, and utility value is lower, and causes the great wasting of resources and environmental pollution.
In general catalysis drying gas, ethylene content is higher, belongs to unsaturated dry gas, and saturated dry gas is usually from PSA stripping gas, and lighter hydrocarbons dry gas, hydrogenation dry gas, reformation dry gas etc., ethane in saturated dry gas, propane content are higher, and ethene, propylene content are very low.Therefore, the concentrate gas composition after saturated dry gas and unsaturated dry-gas recovery and application also differ widely.
Ethane is ideal cracking stock, and in steam-cracking process, sizable Partial Conversion becomes ethene.If by the ethane recovery in oil refinery dry gas, be sent to ethylene producing device, not only take full advantage of refinery exhaust resource, and reduce cracking stock cost, embody Integrated Refinery And Petrochemical advantage.
From oil refinery dry gas, the method for recovered ethylene mainly contains separation by deep refrigeration, middle cold oil absorption process, Separation by Complexation method, pressure swing adsorption process etc. at present, and various method differs from one another.Separation by deep refrigeration technical maturity, Recovery rate of ethylene is high, but investment is large, higher for rare ethylene recovery energy consumption; Separation by Complexation method, Recovery rate of ethylene is higher, but requires strict to the impurity in raw material, and pre-treatment costly, needs special complexes absorption; Pressure swing adsorption process is simple to operate, and energy consumption is lower, but product purity is low, and Recovery rate of ethylene is low, and floor space is large.
Middle cold oil absorption process mainly utilizes the different solubility of absorption agent to component each in gas to carry out separating gas mixture, the general heavy constituent first utilizing absorption agent to absorb C2 and more than C2, isolate the non-condensable gases such as methane, hydrogen, then use each component in the agent of rectification method separate absorbent.The method has the features such as small scale, strong adaptability, investment cost be low.
CN1640992 proposes a kind of refrigeration oil absorption process being absorption agent with the self-produced stable light hydrocarbon of device, is applicable to reclaim liquefied gas from associated gas or Sweet natural gas, and C3 yield requires higher recovery process.Adopt the absorption process of this refrigeration oil, with less absorption agent, can obtain higher light hydrocarbon recovery rate, and technique is simple, energy consumption is lower, better economic benefit.But the method is only applicable to reclaim liquefied gas from associated gas or Sweet natural gas, can not reclaim C2 cut, cannot be used for the recovery of plant catalytic dry gas.
US5502971 discloses a kind of low-pressure low-temperature technique reclaiming C2 and more heavy hydrocarbons, is applicable to the recovery of oil refinery dry gas.This technique eliminates traditional high pressure scheme, changes and adopts low-voltage technology, and such recovered temperature just can remain on the temperature of nitric acid resin generation, avoids dangerous Potential feasibility, can also keep higher olefin yields simultaneously.The process employs low pressure scheme, temperature is low reaches-100 DEG C, belongs to the one of deep cooling process for separating, and investment is comparatively large, and energy consumption is higher.
US6308532 proposes a kind of technique of recovered ethylene and propylene from oil refinery dry gas, this technique comprises extracts C3 out from absorption tower reactor, C4, C5, part tower bottoms phase materials is also circulated to tower top by C6 liquid, thus keep the freezing temp of overhead condenser to be not less than-95 DEG C, in absorption tower, be rich in propylene or ethylene-propylene region extraction gas phase side line simultaneously.Although part kettle material is circulated to tower top and is unlikely too low to keep tower top temperature by this technique, tower top temperature is still low reaches-95 DEG C, still belongs to the one of deep cooling process for separating, and therefore invest comparatively large, energy consumption is higher.
CN101063048A discloses the method for cold oil absorption process separating plant catalytic dry gas in a kind of employing, this technique is made up of steps such as compressing, remove sour gas, drying and purification, absorption, desorb, cold recovery and rough segmentation, there is absorption agent with low cost, lose the advantages such as low.But the method absorption temperature is low, and energy consumption is high, absorption agent internal circulating load is large, and equipment size is large, and process CIMS is complicated, and product purity is not high.In addition, it is gas phase C-2-fraction and ethane that this technique reclaims products obtained therefrom, can only adopt Cemented filling, cause the suitability of the program to be subject to larger restriction.
It is 5 ~ 15 DEG C that CN101812322A discloses absorption temperature, and adopts decompressor and ice chest to reclaim the absorption extraction plant catalytic dry gas method of cold.Although the method increase the rate of recovery of alkene and alkane, flow process relative complex, invests relatively large, and energy consumption is relatively high.
CN101759516A discloses a kind of method of oil-absorption process separating plant catalytic dry gas, and this technique, by compressing, absorbs, desorb, then the step such as absorptions composition, adopts carbon five hydrocarbon as absorption agent, carbon two C3 fraction in recovery catalysis drying gas.But the method is only for reclaiming catalysis drying gas, and Recovery rate of ethylene is low.In addition, carbon two concentrate pneumatic transmission is toward ethylene unit alkaline washing tower, and thus certain needs processes and control foreign matter content in concentrate gas, and in addition, carbon two concentrate pneumatic transmission is comparatively large to the influence on system operation of ethylene unit toward soda-wash tower, and suitability is affected.The technique that patent CN101759518A adopts is identical with CN101759516A, although employing C_4 hydrocarbon is absorption agent, Recovery rate of ethylene is still not high, and concentrate gas is large on ethylene unit impact, and suitability is limited.
In sum, existing oil refinery dry gas is recycled mainly for catalysis drying gas, and only pay close attention to the ethene reclaimed in dry gas, therefore how with utilizing, research is further needed to saturated dry gas and unsaturated dry gas centralized recovery, in addition, there is the problems such as investment is large, energy consumption is high, the rate of recovery is low, technique suitability is limited in existing technique.
Summary of the invention
For solving how to saturated dry gas and unsaturated dry gas centralized recovery and utilization, and there is the problems such as investment is large, energy consumption is high, the rate of recovery is low, technique suitability is limited in existing technique, the invention provides a kind of refinery mixing dry gas recovery system level recovery method.Present invention process comprises two cover compression-absorption-desorption apparatus, shares a reabsorber.Oil refinery dry gas divides saturated dry gas and unsaturated dry gas respectively with the recycling of absorption-desorption method, obtains saturated carbon two concentrate gas product and unsaturated carbon two concentrate gas product, be sent to Furnace of Ethylene Cracking Plant and soda-wash tower respectively from desorption tower tower top.Each absorption tower top gaseous phase is concentrated and is delivered to the unified process of reabsorber.The inventive method rate of recovery is high, and energy consumption is low, runs substantially without impact ethylene unit.
An object of the present invention is to provide a kind of refinery mixing dry gas recovery system.
Comprise:
Unsaturated dry-gas recovery device, saturated dry-gas recovery device and reabsorber;
Unsaturated dry-gas recovery device and saturated dry-gas recovery device comprise respectively: compressor, absorption tower, desorption tower; Compressor connects absorption tower, and absorption tower tower reactor connects desorption tower, and desorption tower tower reactor connects top, absorption tower;
Unsaturated dry-gas recovery device is connected reabsorber respectively with the top, absorption tower in saturated dry-gas recovery device.
Absorption tower tower reactor arranges reboiler.
Two of object of the present invention is to provide a kind of refinery mixing dry gas recovery method.
Comprise:
1) oil refinery dry gas divides saturated dry gas and unsaturated dry gas, enters two absorption towers respectively after compressed cooling;
2) absorption agent enters from top, absorption tower, reclaims C2 and above component in the saturated dry gas in refinery and unsaturated dry gas respectively; The tower reactor logistics on absorption tower delivers to desorption tower respectively, and the logistics of tower top unabsorbed gases is concentrated and is sent to reabsorber;
3) two desorb tower tops obtain saturated concentrate gas and unsaturated concentrate gas, the dry-gas recovery device being raw material with saturated dry gas respectively, obtain saturated concentrate gas at desorb tower top; With the dry-gas recovery that unsaturated dry gas is raw material, obtain unsaturated concentrate gas at desorb tower top; The lean solvent that desorb tower reactor obtains, after cooling, returns to top, absorption tower separately;
4) absorption agent adds from reabsorber top again, reclaims two and absorbs in top gaseous phases by the absorption agent carried secretly with not by carbon two component absorbed.
Concrete technical scheme is as follows:
(1) compress: using the dry gas from refinery catalytic cracking process product as unsaturated dry gas, the dry gas technological processs such as thermally splitting, delayed coking, hydrocracking produced is as saturated dry gas, and carry out compression pressure-raising respectively, pressure brings up to 3.0 ~ 4.5MPa;
(3) cool: the dry gas after the compression obtain described step 1) is cooled to 5 ~ 25 DEG C respectively;
(4) absorb: absorption tower arranges two, and absorption agent enters from top, absorption tower, to absorb in oil refinery dry gas C-2-fraction and more heavy component respectively; Desorption tower process is delivered in the tower reactor logistics on absorption tower; The logistics of tower top unabsorbed gases is sent to reabsorber;
(5) desorb: desorption tower arranges two.Tower reactor logistics from absorption tower enters desorption tower respectively, and the lean solvent that tower reactor obtains is after cooling, and return to top, absorption tower and recycle as absorption agent, tower top obtains gas phase and is sent to ethylene unit respectively.
(6) absorb again: the logistics from absorption tower tower top is concentrated and entered reabsorber, absorption agent adds from reabsorber top again, reabsorber tower top fuel gas is directly discharged into fuel gas pipe network, tower reactor is richness absorption agent again, return refinery's absorption stabilizing apparatus or other device, or directly go ethylene unit to make cracking stock; .
In compression step, oil refinery dry gas generally needs to improve pressure step by step, and preferred pressure brings up to 3.0 ~ 4.5MPa, and to the hop count compressed, there is no particular limitation, preferably adopts two sections or three sections of compressions;
In cooling step, preferably oil refinery dry gas is cooled to 5 ~ 25 DEG C.The cold water that refrigeration agent is optional about 5 DEG C, is provided by lithium-bromide absorption-type refrigerating machine, or adopts other cryogens such as ammonia refrigeration.Preferred lithium-bromide absorption-type refrigerating machine provides cryogen.
In absorption step, described absorption agent can for the C-4-fraction containing normal butane, Trimethylmethane, the saturated liquefied gas containing saturated carbon three and carbon four, or the C5 fraction containing Skellysolve A, iso-pentane.Preferred normal butane and saturated liquefied gas are as absorption agent.
In the method for the invention, to the not special requirement of absorption agent consumption, those skilled in the art can determine according to the general knowledge of prior art.
Described absorption tower Optimization Theory plate number is 25 ~ 60, and working 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 is sent to reabsorber.Absorption agent enters from tower top again, and absorb by the absorption agent taken out of with not by carbon two component absorbed, reabsorber top gaseous phase is directly discharged into fuel gas pipe network, and the extraction of tower reactor liquid phase is sent to outside battery limit (BL); Described absorption agent is again gasoline, or heavy naphtha, Aromatic raffinate etc., the stable gasoline component of preferred refinery.
The number of theoretical plate of preferred described reabsorber is 10-50, and working pressure is 1.0-4.0MPa.
In desorption procedure, because the pressure of the tower reactor logistics from absorption tower and desorption tower exist pressure reduction, pressure reduction is therefore relied on to enter desorption tower.Absorption agent after the desorb that desorption tower tower reactor obtains returns absorption tower recycle after cooling step by step.Absorption agent can enter reabsorber with absorption top gaseous phase, therefore, preferably introduces one absorption agent as a supplement in desorb tower reactor, with absorptive tower absorbent consumption in guarantee system.
The number of theoretical plate of preferred described desorption tower is 20-60, and working pressure is 1.0-4.0MPa.
Main containing the ethene of 20-80wt%, the ethane of 5-40wt% in unsaturated concentrate gas, the content sum of each component is no more than 100%.
The main ethane containing 50-90wt% in saturated concentrate gas, the propane of 5-30wt%, the content sum of each component is no more than 100%.
In the present invention, absorption tower tower reactor arranges reboiler, to ensure that absorbing the light constituents such as tower reactor methane, hydrogen drops to below setting requirement.Wherein absorption tower tower reactor reboiler and desorption tower tower reactor reboiler heating medium can adopt low-pressure steam, also can adopt deep fat, preferred deep fat heating, can make full use of the rich heat in refinery, also can reduce process energy consumption.
Method of the present invention also comprises and removes sour gas step, but only carries out the process of acid gas removal body to unsaturated dry gas.At unsaturated dry gas through boost intersegmental of compressor or carry out the process of acid gas removal body after desorption tower, amine can be adopted to wash, alkali cleaning also can be adopted to remove sour gas, preferably remove sour gas after desorption, preferred alkali wash acid gas removal body.
Method of the present invention also comprises deoxidation treatment, but only carries out deoxidation treatment to unsaturated dry gas, reductor preferred Beijing Chemical Research Institute BC-TOS-15 dehydrogenation catalyst.
Refinery of the present invention mixing dry gas Application way has following characteristics:
1) in method of the present invention, the saturated dry gas in refinery and unsaturated dry gas carry out absorption and desorption respectively, the concentrate gas obtained is sent to Furnace of Ethylene Cracking Plant and soda-wash tower respectively, this invented technology has given full play to saturated concentrate gas and unsaturated concentrate gas advantage, and the disadvantageous effect avoided ethylene unit, in addition, this technique absorption temperature is higher, be separated relative to after mixing dry gas absorption-desorb, energy consumption reduces clearly again.
2) method of the present invention is without any requirement to oil refinery dry gas, and saturated dry gas and unsaturated dry gas recycle respectively, and the suitability of technique is strong.
3) the present invention adopts the low-grade deep fat heating in refinery, and energy consumption reduces greatly.
4) absorption agent selectivity is comparatively large, and each absorption agent assimilation effect is all more satisfactory, according to different manufacturers situation, can select optimum absorption agent
Accompanying drawing explanation
Fig. 1 is refinery of the present invention mixing dry gas recovery system schematic diagram.
Description of reference numerals:
1,1# compresses suction tank; 2,1# compressor; 3,1# absorption tower; 4,1# desorption tower; 5,2# compresses suction tank; 6,2# compressor; 7,2# absorption tower; 8,2# desorption tower; 9, reabsorber; 10, fuel gas; 11, rich gasoline; 12 unsaturated concentrate gas; 13 saturated concentrate gas; 14 carbon four absorption agents supplemented; 15 lighter hydrocarbons; 16 unsaturated dry gas; 17 saturated dry gas
Embodiment
Below in conjunction with embodiment, further illustrate the present invention.
Embodiment:
As shown in Figure 1, a kind of refinery mixing dry gas recovery system, unsaturated dry-gas recovery device, saturated dry-gas recovery device and reabsorber; Unsaturated dry-gas recovery device and saturated dry-gas recovery device comprise respectively: compressor, absorption tower, desorption tower; Compressor connects absorption tower, and absorption tower tower reactor connects desorption tower, and desorption tower tower reactor connects top, absorption tower; Unsaturated dry-gas recovery device is connected reabsorber respectively with the top, absorption tower in saturated dry-gas recovery device.Absorption tower tower reactor arranges reboiler.
Dry gas composition is as shown in table 1,
Table 1
| Catalysis drying gas | Coking dry gas | PSA stripping gas | |
| mol% | mol% | mol% | |
| Hydrogen | 24.74 | 11.74 | 30.35 |
| Nitrogen | 18.85 | 0 | 1.4 |
| Oxygen | 0.69 | 0 | 0.4 |
| CO | 0 | 0 | 0 |
| CO2 | 2.23 | 0 | 0 |
| H2S | 0 | 0.06 | 0 |
| Methane | 25.86 | 59.92 | 34.58 |
| Ethane | 11.7 | 21.89 | 12.76 |
| Ethene | 14.28 | 2.6 | 0 |
| Propane | 0.1 | 3.06 | 10.11 |
| Propylene | 0.78 | 0 | 0 |
| Trimethylmethane | 0 | 0 | 1.62 |
| Normal butane | 0.09 | 0 | 2.23 |
| Iso-pentane | 0 | 0 | 0.05 |
| Skellysolve A | 0 | 0 | 0.89 |
| >C5 | 0 | 0 | 0.04 |
| Water | 0.68 | 0.73 | 0.48 |
Oil refinery dry gas has catalysis drying gas, coking dry gas, PSA stripping gas is formed, wherein catalysis drying gas is unsaturated dry gas, and coking dry gas and PSA stripping gas do saturated dry gas process, and supplied materials is total up to 46785kg/h, saturated dry gas supplied materials pressure is 0.03MPag, unsaturated dry gas supplied materials pressure is 0.8Mpag, selects normal butane as absorption agent, reclaims the carbon two in oil refinery dry gas and carbon three components.
Comprise the following steps:
(1) compress: in oil refinery dry gas, catalysis drying gas is as unsaturated dry gas process, and through two sections of compressions, pressure is increased to 4MPag, is cooled to 15 DEG C and enters absorption tower; Coking dry gas and PSA stripping gas are as saturated dry gas process, and through four sections of compressions, pressure is increased to 4MPag, is cooled to 15 DEG C and enters absorption tower;
(2) absorb: the number of theoretical plate on 1# absorption tower and 2# absorption tower is 38, and working pressure is 3.9MPag, tower top temperature 20 DEG C.Lyosorption used is normal butane, and solvent enters in tower from absorbing tower jacking, and dry gas enters from the 25th block of column plate.Carbon two in dry gas and heavy constituent thereof are got off by solvent absorbing, and from tower reactor extraction, tower top is the light constituent such as methane, hydrogen, and is entrained with a small amount of absorption agent, is sent to naphtha scrubber.
(3) desorb: the number of theoretical plate of 1# desorption tower and 2# desorption tower is 41, and working pressure is 2.2MPag.Top gaseous phase after desorb is as product extraction, and lean solvent is cooled to 15 DEG C and returns to absorption tower and recycle after stage-by-stage heat exchange.For ensureing purity and the consumption on 1# absorption tower and 2# absorptive tower absorbent, extraction part lean solvent before lean solvent returns to absorption tower, and supplement fresh absorbent.The lean solvent of extraction converges and is sent to ethylene unit lighter hydrocarbons stove as one of product afterwards.
(4) absorb again: the number of theoretical plate of reabsorber is 20, and working pressure is 3.8MPag.Absorption agent is stable gasoline again, and stable gasoline enters in tower from tower top, reclaims by the mode absorbed the absorption agent and unabsorbed carbon two component carried secretly.Naphtha scrubber top gaseous phase is sent to fuel gas pipe network, and tower reactor liquid phase is sent to gasoline desorption tower.
(5) purify: the unsaturated concentrate gas obtained is removed oxygen through deoxidation reactor, and working pressure is 2.0MPa, and temperature is 100 DEG C ~ 300 DEG C; Adopt soda-wash tower to remove sour gas, working pressure is 1.0 ~ 2.0MPa, and temperature is 40 DEG C ~ 50 DEG C; Unsaturated concentrate pneumatic transmission after purification is toward the soda-wash tower of ethylene unit.
The unsaturated concentrate gas 12 obtained is 9378kg/h, and product composition is in table 2.
Table 2
| Composition | mol% |
| Hydrogen | 0.03 |
| CO2 | 0.02 |
| Methane | 4.98 |
| Ethene | 44.15 |
| Ethane | 40.47 |
| Propylene | 2.37 |
| Propane | 0.92 |
| Trimethylmethane | 1.54 |
| Normal butane | 5.10 |
| Iso-pentane | 0.01 |
| Water | 0.42 |
Saturated concentrate gas 13 product obtained is 15054kg/h, and composition is in table 3.
Table 3
Lighter hydrocarbons 15 product obtained is 6723kg/h, and composition is in table 4.
Table 4
| Composition | mol% |
| Hydrogen | 0.02 |
| Nitrogen | 0.03 |
| CO2 | 0.08 |
| Methane | 1.07 |
| Ethene | 0.27 |
| Ethane | 1.99 |
| Propylene | 0.18 |
| Propane | 17.61 |
| Trimethylmethane | 13.81 |
| Normal butane | 36.73 |
| Iso-pentane | 17.34 |
| Skellysolve A | 6.48 |
| Positive amylene | 2.13 |
| Pentamethylene | 0.33 |
| >C5 | 1.75 |
| Benzene | 0.12 |
| Toluene | 0.01 |
| Water | 0.05 |
In the present embodiment, carbon two rate of recovery is 96.33%.
Claims (7)
1. refinery's mixing dry gas recovery system, is characterized in that described system comprises:
Unsaturated dry-gas recovery device, saturated dry-gas recovery device and reabsorber;
Unsaturated dry-gas recovery device and saturated dry-gas recovery device comprise respectively: compressor, absorption tower, desorption tower; Compressor connects absorption tower, and absorption tower tower reactor connects desorption tower, and desorption tower tower reactor connects top, absorption tower;
Unsaturated dry-gas recovery device is connected reabsorber respectively with the top, absorption tower in saturated dry-gas recovery device.
2. oil refinery dry gas recovery system as claimed in claim 1, is characterized in that:
Absorption tower tower reactor arranges reboiler.
3. adopt a recovery method for refinery as claimed in claim 1 or 2 mixing dry gas recovery system, it is characterized in that described method comprises:
1) oil refinery dry gas divides saturated dry gas and unsaturated dry gas, enters two absorption towers respectively after compressed cooling;
2) absorption agent enters from top, absorption tower, reclaims C2 and above component in the saturated dry gas in refinery and unsaturated dry gas respectively; The tower reactor logistics on absorption tower delivers to desorption tower respectively, and the logistics of tower top unabsorbed gases is concentrated and is sent to reabsorber;
3) two desorb tower tops obtain saturated concentrate gas and unsaturated concentrate gas respectively, and the lean solvent that desorb tower reactor obtains, after cooling, returns to top, absorption tower separately;
4) absorption agent adds from reabsorber top again, reclaims two and absorbs in top gaseous phases by the absorption agent carried secretly with not by carbon two component absorbed.
4. mixing dry gas recovery method as claimed in claim 3, is characterized in that:
Saturated dry gas and unsaturated dry gas, compressed to 3.0 ~ 4.5MPa respectively, enter two absorption towers after being cooled to 5 ~ 25 DEG C.
5. mixing dry gas recovery method as claimed in claim 3, is characterized in that:
In step (2), described absorption agent is the C-4-fraction containing normal butane, Trimethylmethane, the saturated liquefied gas containing saturated carbon three and carbon four, or the C5 fraction containing Skellysolve A, iso-pentane;
In step (4), described absorption agent is again gasoline, heavy naphtha or Aromatic raffinate.
6. the mixing dry gas recovery method as described in one of claim 3 ~ 5, is characterized in that:
Absorption tower number of theoretical plate is 25 ~ 60, and working pressure is 3.0 ~ 6.0MPa, and tower top temperature is 10 DEG C ~ 40 DEG C;
The number of theoretical plate of desorption tower is 20-60, and working pressure is 1.0-4.0MPa;
The number of theoretical plate of reabsorber is 10-50, and working pressure is 1.0-4.0MPa.
7. mixing dry gas recovery method as claimed in claim 6, is characterized in that:
The process of acid gas removal body and/or deoxidation treatment are carried out to unsaturated dry gas.
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112759568A (en) * | 2019-11-01 | 2021-05-07 | 中国石油化工股份有限公司 | Method and device for treating benzene-containing dry gas and preparing maleic anhydride |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101759518A (en) * | 2008-12-25 | 2010-06-30 | 中国石油化工股份有限公司 | Method for absorbing and separating refinery catalytic dry gas by adopting oil |
| CN101759516A (en) * | 2008-12-25 | 2010-06-30 | 中国石油化工股份有限公司 | Method for refining catalysis drying gas by using oil absorption extraction |
| CN101812322A (en) * | 2009-02-19 | 2010-08-25 | 中国石油化工股份有限公司 | Method for separating refinery catalytic dry gas by adopting oil absorption |
| CN103087772A (en) * | 2011-11-02 | 2013-05-08 | 中国石油化工股份有限公司 | Device and method for separating refinery dry gas through oil absorption |
-
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- 2013-10-23 CN CN201310504588.XA patent/CN104557385B/en active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101759518A (en) * | 2008-12-25 | 2010-06-30 | 中国石油化工股份有限公司 | Method for absorbing and separating refinery catalytic dry gas by adopting oil |
| CN101759516A (en) * | 2008-12-25 | 2010-06-30 | 中国石油化工股份有限公司 | Method for refining catalysis drying gas by using oil absorption extraction |
| CN101812322A (en) * | 2009-02-19 | 2010-08-25 | 中国石油化工股份有限公司 | Method for separating refinery catalytic dry gas by adopting oil absorption |
| CN103087772A (en) * | 2011-11-02 | 2013-05-08 | 中国石油化工股份有限公司 | Device and method for separating refinery dry gas through oil absorption |
Non-Patent Citations (1)
| Title |
|---|
| 高计皂 等: ""炼厂干气回收技术现状及进展"", 《广东化工》, vol. 40, no. 16, 30 August 2013 (2013-08-30), pages 127 - 128 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112759568A (en) * | 2019-11-01 | 2021-05-07 | 中国石油化工股份有限公司 | Method and device for treating benzene-containing dry gas and preparing maleic anhydride |
| CN112759568B (en) * | 2019-11-01 | 2022-08-19 | 中国石油化工股份有限公司 | Method and device for treating benzene-containing dry gas and preparing maleic anhydride |
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