CN1891328A - Low concentration adsorbable contituent variable-pressure adsorption and separation method - Google Patents
Low concentration adsorbable contituent variable-pressure adsorption and separation method Download PDFInfo
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- CN1891328A CN1891328A CNA200610078714XA CN200610078714A CN1891328A CN 1891328 A CN1891328 A CN 1891328A CN A200610078714X A CNA200610078714X A CN A200610078714XA CN 200610078714 A CN200610078714 A CN 200610078714A CN 1891328 A CN1891328 A CN 1891328A
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
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- Y02P20/50—Improvements relating to the production of bulk chemicals
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Abstract
This invention discloses a serial adsorption method for concentrating effective gas of a low concentration and adsorbent gas, in which, a mixed gas with the gas concentration of 4-20% is called raw material gas and the increasing method for the concentration of its effective gas includes: utilizing a transformation adsorption gas separation technology to carry out the following steps: 1, the raw material gas pressure is 0.02-0.4MPa and a multi-state transformation adsorbing technology to concentrate the effective gas, firstly, the adsorbed output effective gas reduces its concentration to 40-70% to the raw material gas, secondly, the concentration of said output effective gas is reduced to 40-70% of the 2 raw material gas, thirdly, the concentration of the effective gas of the output is 40-70% of the 3 raw material gas, so on so forth, the second stage is used at least and the fifth is used to the most based on the recovery.
Description
One, technical field
The present invention relates to the gas separation field, is a kind of method of using part component in the pressure swing adsorption separating gas mixture.
Two, background technology
For the technology of flue gas recovery carbon dioxide component, the method for usually using is hydrometallurgic recovery.Owing to need huge equipment and more operation energy consumption, therefore, often have to utilize other carbonated gases to replace flue gas, need investment much to be used for constructing device equally.
For the technology of cracking gas recovery ethylene component, the method for usually using is that alternating temperature absorption is reclaimed.Since need huge equipment and 1 more operation energy consumption, therefore, many users, directly the ethene waste gas that contains with low concentration, low-pressure directly burns, and has reduced the value of ethene in the cracking gas.
Use light concentration gas as industrial chemicals, general because the active ingredient branch forces down, and the reaction motive force is little, is unfavorable for the raising of utilization rate of equipment and installations, therefore, must be by improving gas concentration or improving gas pressure and realize that the active ingredient dividing potential drop improves.The light concentration gas compression certainly will consume a large amount of idle works, therefore, improves gas concentration, becomes a valid approach.
Pressure swing adsorption is used to put forward the concentration carbon dioxide technology all has application in a lot of environments for use, and still, unstripped gas concentration is generally all more than 20%.This is owing to carbon dioxide in the unstripped gas is low excessively, if unstripped gas is brought up to very high pressure, certainly will waste the very high energy.Therefore the recycling of low concentration of carbon dioxide 4～15% is considered to a kind of uneconomic behavior always.
Three, summary of the invention
In order to reclaim low concentration available gas composition, the present invention utilizes the strategy of plural serial stage absorption, is used for improving gas reclaiming rate.
In order to reduce energy consumption, can use lower adsorptive pressure.Before using pressure swing absorption process recovery low concentration available gas, must guarantee raw gas pressure 0.02～0.4MPa (table), through preliminary treatment, remove the component that boiling point is higher than available gas.
To contain low concentration available gas gaseous mixture and under lower pressure 0.02～0.4MPa, send into adsorption tower, in first order adsorption tower, it is attached that available gas is adsorbed agent, and the first order absorption effluent gases lower than unstripped gas available gas concentration directly sent into second level adsorption tower; In the adsorption tower of the second level, available gas is adsorbed agent absorption, and sends into third level adsorption tower than the lower second level absorption effluent gases direct 2 of first order absorption effluent gases available gas concentration; In third level adsorption tower, available gas is adsorbed agent absorption, and directly sends into fourth stage adsorption tower than the lower third level absorption effluent gases of second level absorption effluent gases available gas concentration; The rest may be inferred, can be according to the requirement of the rate of recovery, and adsorption tower progression is secondary at least, can reach Pyatyi at most.
The utilization desorb adsorption tower of finding time.
Use the corresponding levels or next stage the reflux non-available gas gas of displacement adsorption tower dead space of stripping gas of finding time, improve the adsorption tower available gas concentration in the stripping gas of finding time thus.
Next stage can be found time gas as upper level or more the unstripped gas of upper level be mixed into adsorption tower.
Like this, the gas available gas concentration of finding time of the first order can reach 150～500% of unstripped gas available gas concentration.
The unstripped gas that the present invention is alleged, can be in flue gas, stove gas, the low pressure flash gas, cracking gas, or the like.
The available gas composition that the present invention is alleged can be that available gas, carbon monoxide, methane, ethane, propane, butane, ethene, acetylene, nitrogen, oxygen, argon gas, helium, sulfur dioxide, hydrogen sulfide and other can be used as the available raw materials of specialty such as chemical industry, metallurgy, aviation.
The pressure swing adsorption technique that the present invention is alleged can be that 2～12 adsorption towers are formed each level.
Four, the specific embodiment
Embodiment 1: certain flue gas available gas gas concentration lwevel 6% needs to improve more than the gas concentration lwevel to 14%.
(1) be 0.12MPa (table) through being compressed to pressure,, remove the low-boiling composition of ratio available gas in the unstripped gas through preliminary clearning, such as, sulfur dioxide, hydrogen sulfide, coal tar, benzene and derivative thereof, or the like; (2) use 33 grades of pressure-changed adsorption concentrating technologies: first order imported raw material gas available gas concentration 6%, first order adsorption tower effluent gases available gas concentration 4.2%, first order exhaust available gas concentration 15%; Second level imported raw material gas is first order adsorption tower effluent gases, available gas concentration 4.2%, and second level adsorption tower effluent gases available gas concentration 3.0%, second level exhaust available gas concentration 10% is returned the first order as displacement gas; Third level imported raw material gas is second level adsorption tower effluent gases, available gas concentration 3.0%, and third level adsorption tower effluent gases available gas concentration 2.0%, third level exhaust available gas concentration 6% is returned the first order as unstripped gas.
As product gas, available gas concentration reaches about 15% by first order exhaust extension.
Embodiment 2: certain flue gas available gas concentration 12% needs to improve more than the concentration to 35%.
(1) be 0.15MPa (table) through being compressed to pressure,, remove the low-boiling composition of ratio available gas in the unstripped gas through preliminary clearning, such as, sulfur dioxide, hydrogen sulfide, coal tar, benzene and derivative thereof, or the like; (2) use level Four pressure-changed adsorption concentrating technology: first order imported raw material gas available gas concentration 12%, first order adsorption tower effluent gases available gas concentration 8.4%, first order exhaust available gas concentration 35%; Second level imported raw material gas is first order adsorption tower effluent gases, available gas concentration 8.4%, and second level adsorption tower effluent gases available gas concentration 6.0%, second level exhaust available gas concentration 16% is returned the first order as displacement gas; Third level imported raw material gas is second level adsorption tower effluent gases, available gas concentration 6.0%, and third level adsorption tower effluent gases available gas concentration 4.4%, third level exhaust available gas concentration 12% is returned the first order as unstripped gas; Fourth stage imported raw material gas is third level adsorption tower effluent gases, available gas concentration 4.4%, and the fourth stage 4 adsorption tower effluent gases available gas concentration 3.2%, third level exhaust available gas concentration 8% is returned the second level as unstripped gas.
As product gas, available gas concentration reaches about 35% by first order exhaust extension.
Embodiment 3: certain stove gas carbon monoxide gas concentration 8% needs to improve more than the concentration to 50%.
(1) be 0.05MPa (table) through being compressed to pressure,, remove the low-boiling composition of ratio available gas in the unstripped gas through preliminary clearning, such as, carbon dioxide, sulfur dioxide, hydrogen sulfide, coal tar, benzene and derivative thereof, or the like; (2) use secondary pressure-changed adsorption concentrating technology: first order imported raw material gas available gas concentration 8%, first order adsorption tower effluent gases available gas concentration 6%, first order exhaust available gas concentration 51%; Second level imported raw material gas is first order adsorption tower effluent gases, available gas concentration 6%, and second level adsorption tower effluent gases available gas concentration 4.4%, second level exhaust available gas concentration 15% is returned the first order as displacement gas.
As product gas, available gas concentration reaches about 51% by first order exhaust extension.
Embodiment 4: certain cracking ethylene gas concentration 4% of dropping a hint needs to improve more than the concentration to 88%.
(1) pressure of this gas own is 0.15MPa (table), through preliminary clearning, removes the low-boiling composition of ratio available gas in the unstripped gas, such as, senior rare hydrocarbon or the like; (2) use secondary pressure-changed adsorption concentrating technology: first order imported raw material gas available gas concentration 4%, first order adsorption tower effluent gases available gas concentration 3%, first order exhaust available gas concentration 20%; Second level imported raw material gas is that the first order is adsorbed 5 tower effluent gases, available gas concentration 3%, and second level adsorption tower effluent gases available gas concentration 2%, second level exhaust available gas concentration 10% is returned the first order as displacement gas.
As intermediate products gas, available gas concentration reaches about 18% by first order exhaust extension.
Use for the second time this patent, continue to improve ethylene concentration to qualified 88%.
(1) improving the intermediate products gas pressure is 0.35MPa (table); (2) use secondary pressure-changed adsorption concentrating technology: first order imported raw material gas available gas concentration 20%, first order adsorption tower effluent gases available gas concentration 8%, first order exhaust available gas concentration 88%; Second level imported raw material gas is first order adsorption tower effluent gases, available gas concentration 8%, and second level adsorption tower effluent gases available gas concentration 4%, second level exhaust available gas concentration 44% is returned the first order as displacement gas.
Absorption effluent gases in the second level is as the first order unstripped gas that uses for the first time patent device.
As intermediate products gas, available gas concentration reaches 88% by first order exhaust extension.
This patent reclaims carbon monoxide through actual the use at flue gas recovery carbon dioxide, cracking gas recovery ethene, synthetic ammonia copper gas washing, and effect is fairly obvious, effectively reduces the energy consumption in the gas removal process, has saved cost.
Claims (3)
1, a kind of gaseous mixture that contains effective gas composition concentration 4～20% is called unstripped gas, the method that its available gas concentration improves, it is characterized in that, use adsorption gas separating technology, and the following step of process: (1) raw gas pressure 0.02～0.4MPa; Use the stage variable pressure absorbing process to carry dense available gas: the first order, absorption exit gas available gas concentration is reduced to 40～70% of unstripped gas concentration; The second level, absorption exit gas available gas concentration is reduced to (40～70%) 2 of unstripped gas concentration; The third level, absorption exit gas available gas concentration is reduced to (40～70%) of unstripped gas concentration
3The rest may be inferred, can be according to rate of recovery needs, and minimum use secondary can only use Pyatyi at most; (2) gas of finding time that uses the corresponding levels or next stage is replaced adsorption tower as substitution gas, improves the available gas concentration in the gas of finding time thus; (3) with the gas of finding time of the corresponding levels as the upper level or the unstripped gas of upper level more; (4) the find time available gas concentration of gas of the first order can reach 150～500% of unstripped gas available gas concentration.
2, the alleged unstripped gas of claim 1, can be in flue gas, stove gas, the low pressure flash gas, cracking gas is dropped a hint, other is dropped a hint, or the like.
3, the alleged available gas composition of claim 1 can be that carbon dioxide, carbon monoxide, methane, ethane, propane, butane, ethene, acetylene, nitrogen, oxygen, argon gas, helium, sulfur dioxide, hydrogen sulfide and other can be used as the available raw materials of specialty such as chemical industry, metallurgy, aviation.
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| Application Number | Priority Date | Filing Date | Title |
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| CN200610078714XA CN1891328B (en) | 2006-05-10 | 2006-05-10 | Low concentration adsorbable constituent variable-pressure adsorption and separation method |
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| CN200610078714XA CN1891328B (en) | 2006-05-10 | 2006-05-10 | Low concentration adsorbable constituent variable-pressure adsorption and separation method |
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| CN1891328A true CN1891328A (en) | 2007-01-10 |
| CN1891328B CN1891328B (en) | 2011-06-08 |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101503335A (en) * | 2009-02-17 | 2009-08-12 | 杨皓 | Method for concentrating methane by gas pressure swing adsorption of low concentration methane |
| CN104415643A (en) * | 2013-08-20 | 2015-03-18 | 中国石油化工股份有限公司 | Method for selectively removing H2S from gas flow containing CO2 |
| CN108392948A (en) * | 2018-03-21 | 2018-08-14 | 山东京博石油化工有限公司 | A kind of purifying technique and device of hydrogen sulfide |
| CN108545697A (en) * | 2018-04-27 | 2018-09-18 | 杨皓 | A kind of Water gas shift/WGS gas manufacture ammonia synthesis gas technique |
| CN111140862A (en) * | 2019-12-27 | 2020-05-12 | 安徽海德化工科技有限公司 | High-purity n-butane production device |
| CN113735079A (en) * | 2020-12-31 | 2021-12-03 | 李保军 | Method for extracting ultra-high purity helium gas at normal temperature and production device |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1029552C (en) * | 1991-08-24 | 1995-08-23 | 化学工业部西南化工研究院 | Pressure swing adsorption process for removing carbon dioxide from ammonia plant shift gas |
| FR2692245B1 (en) * | 1992-06-10 | 1995-01-20 | Air Liquide | Process and installation for the combined production of synthetic ammonia and pure hydrogen. |
| CN1040292C (en) * | 1992-12-03 | 1998-10-21 | 黄家鹄 | Gas separation method by pressure swing adsorption for simultaneously preparing two gas products with high-purity and high-yield |
| CN1073875C (en) * | 1997-10-24 | 2001-10-31 | 化学工业部西南化工研究设计院 | Pressure swing adsorption process for separating carbon monooxide from carbon monooxide contg. mixed gas |
| CN1344580A (en) * | 2000-09-29 | 2002-04-17 | 陈胜飞 | Pressure swing adsorption method and apparatus for separating gases |
| CN1283344C (en) * | 2001-07-31 | 2006-11-08 | 成都天立化工科技有限公司 | Two-sectional variable pressure adsorption and decarbonizing process of recovering hydrogen and nitrogen gas for urea production |
-
2006
- 2006-05-10 CN CN200610078714XA patent/CN1891328B/en not_active Expired - Fee Related
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101503335A (en) * | 2009-02-17 | 2009-08-12 | 杨皓 | Method for concentrating methane by gas pressure swing adsorption of low concentration methane |
| CN104415643A (en) * | 2013-08-20 | 2015-03-18 | 中国石油化工股份有限公司 | Method for selectively removing H2S from gas flow containing CO2 |
| CN108392948A (en) * | 2018-03-21 | 2018-08-14 | 山东京博石油化工有限公司 | A kind of purifying technique and device of hydrogen sulfide |
| CN108545697A (en) * | 2018-04-27 | 2018-09-18 | 杨皓 | A kind of Water gas shift/WGS gas manufacture ammonia synthesis gas technique |
| CN111140862A (en) * | 2019-12-27 | 2020-05-12 | 安徽海德化工科技有限公司 | High-purity n-butane production device |
| CN113735079A (en) * | 2020-12-31 | 2021-12-03 | 李保军 | Method for extracting ultra-high purity helium gas at normal temperature and production device |
| CN113735079B (en) * | 2020-12-31 | 2023-10-27 | 李保军 | Method and production device for extracting ultra-high purity helium at normal temperature |
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| CN1891328B (en) | 2011-06-08 |
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Granted publication date: 20110608 Termination date: 20180510 |