CN101514137B - Method for removing trace sulfur in styrene by catalytic rectification - Google Patents

Method for removing trace sulfur in styrene by catalytic rectification Download PDF

Info

Publication number
CN101514137B
CN101514137B CN2008100431327A CN200810043132A CN101514137B CN 101514137 B CN101514137 B CN 101514137B CN 2008100431327 A CN2008100431327 A CN 2008100431327A CN 200810043132 A CN200810043132 A CN 200810043132A CN 101514137 B CN101514137 B CN 101514137B
Authority
CN
China
Prior art keywords
sulfur
vinylbenzene
styrene
butylene
iso
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN2008100431327A
Other languages
Chinese (zh)
Other versions
CN101514137A (en
Inventor
钟禄平
肖剑
郭艳姿
卢咏琰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
China Petroleum and Chemical Corp
Sinopec Shanghai Research Institute of Petrochemical Technology
Original Assignee
China Petroleum and Chemical Corp
Sinopec Shanghai Research Institute of Petrochemical Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by China Petroleum and Chemical Corp, Sinopec Shanghai Research Institute of Petrochemical Technology filed Critical China Petroleum and Chemical Corp
Priority to CN2008100431327A priority Critical patent/CN101514137B/en
Publication of CN101514137A publication Critical patent/CN101514137A/en
Application granted granted Critical
Publication of CN101514137B publication Critical patent/CN101514137B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

The invention relates to a method for removing trace sulfur in styrene by catalytic rectification, which mainly solves the problem of difficult removal of the trace sulfur in the styrene recovered from pyrolysis gasoline. The method comprises the following steps that: sulfur-containing styrene (the sulfur content is less than or equal to 500ppm) and isobutene enter from a stripping section and the tower bottom of a catalytic distillation tower respectively, a sulfur-containing component in the styrene and the isobutene react to form a heavy component in a reaction section, the separation of the styrene and the generated heavy component is realized in the catalytic distillation tower at the same time, the tower top is provided with a fractional condenser, isobutene is extracted by a gas phase, desulfurized styrene is extracted by a liquid phase, the sulfur content is less than or equal to 10ppm, and the styrene containing the heavy component sulfur is obtained in the tower. The technical proposal better solves the problem, and can be used for industrial application of the trace sulfur removal in the styrene recovered from the pyrolysis gasoline.

Description

Catalytic distillation removes the method for Determination of Trace Sulfur in the vinylbenzene
Technical field
The present invention relates to the method that a kind of catalytic distillation removes Determination of Trace Sulfur in the vinylbenzene.
Background technology
Adopting naphthas is in the ethylene cracker of raw material, and the content of its YLENE is 0.06~0.07 ton of/ton ethene, and pyrolysis gasoline C 8YLENE in the cut: vinylbenzene: the ratio of ethylbenzene is generally 4: 3: 1.Calculate in view of the above, the ethylene unit that a cover is 600,000 tons/year, recyclable vinylbenzene is about 2.9 ten thousand tons/year, if ethylbenzene dehydrogenation is wherein reclaimed, vinylbenzene output also can improve, and has certain recovery value.From pyrolysis gasoline, reclaim vinylbenzene and can eliminate the hydrogen gas consumption of vinylbenzene hydrogenation in traditional pyrolysis gasoline device, thereby alleviate the load of hydrogenation unit; The ethyl-benzene level that reclaims in the Mixed XYLENE significantly reduces, and can be used as the raw material that xylene isomerization is produced p-Xylol; Recyclable a considerable amount of vinylbenzene.
Pyrolysis gasoline C 8Cut is through behind extracting rectifying, solvent recuperation and commercial benzene ethene three rectification cells, obtains purity and be 99.9% vinylbenzene, but the sulphur content in the vinylbenzene more than 150ppm, can't be as the raw material of some polymer production.There are not sulfur-bearing removes in the relevant recycling vinyl benzene with pyrolysis gasoline document and patent report at present.
Introduce the technology that a kind of catalytic distillation removes sulfur-bearing in the petroleum hydrocarbon among the patent CN1412279A; Through removing of sulfur component in the coupling realization petroleum hydrocarbon of catalytic hydrogenation reaction and rectifying; Overhead distillate is no sulphur petroleum hydrocarbon, and the tower still obtains the heavy constituent sulphur after the hydrogenation reaction.Introduced the method that a kind of oil by catalytic oxidation and extracting and separating removes among the patent CN1683476A; This method is oxygenant with the hydrogen peroxide; The mineral acid of tungstenic and the mixture of quaternary ammonium salt are catalyzer, and with organic sulfide catalyzed oxidations such as the thionaphthene in the sour product, dibenzothiophene, the oil product after the catalyzed reaction uses the acetonitrile/water azeotrope to extract as extraction agent; And then reaction product is transferred to the polar solvent phase, realize desulfurizing oil.Patent WO2005/073348 has introduced a kind of sulfur method of hydrocarbon ils, has the gac of transistion metal compound to contact through hydrocarbon ils and strong solid acid catalyst or load, carries out desulfurization.
Summary of the invention
The present invention relates to the method that a kind of catalytic distillation removes Determination of Trace Sulfur in the vinylbenzene, mainly solve the problem that from the vinylbenzene that pyrolysis gasoline reclaims Determination of Trace Sulfur removes difficulty, provide a kind of catalytic distillation to remove the method for Determination of Trace Sulfur in the recycling vinyl benzene with pyrolysis gasoline.This method has the high characteristics of desulfuration efficiency.
In order to solve the problems of the technologies described above; The technical scheme that the present invention adopts is following: a kind of catalytic distillation removes the method for Determination of Trace Sulfur in the vinylbenzene, it is characterized in that sulphur content is not more than the sulfur-bearing vinylbenzene of 500ppm, iso-butylene and at the bottom of the stripping section of catalytic rectifying tower and tower, gets into respectively, and sulfur component in the vinylbenzene and iso-butylene react the generation heavy constituent at conversion zone; Vinylbenzene is realized separating in catalytic rectifying tower with the heavy constituent of generation simultaneously; Cat head is provided with partial condenser, the unreacted iso-butylene of gas phase extraction, liquid phase extraction desulfurization vinylbenzene; Sulphur content≤10ppm, the tower still obtains containing the vinylbenzene of heavy constituent sulphur.
In technique scheme, the theoretical number of plates of rectifying section preferred version of catalytic rectifying tower is 10~30, and stripping section number of theoretical plate preferred version is 10~30, and the height of conversion zone is equivalent to the height of 5~20 theoretical stages; The sulfur component raw materials components mole ratio is 1~30 in iso-butylene and the styrene material, and reflux ratio is 0.3~6, and recovery ratio is 90~98%, and working pressure is 4~20KPa; Sulfur component raw materials components mole ratio preferable range is 5~10 in iso-butylene and the styrene material, and the reflux ratio preferable range is 0.7~1.5, and the recovery ratio preferable range is 92~95%, and the working pressure preferable range is 8~12KPa; The conversion zone catalyst filling is at least a in acidic ion exchange resin or the solid acid catalyst.
Sulfur component is a thiophenes in the vinylbenzene that pyrolysis gasoline reclaims; And this sulfur component and cinnamic boiling point are more approaching; Can't realize separating through rectifying; Because thiophenes and iso-butylene can alkylation generate heavy constituent sulphur under the acid catalyst effect, heavy constituent can be used rectifying separation with vinylbenzene again, thereby sulfur component removes in the realization vinylbenzene.The present invention is through the technical scheme of catalytic distillation, reached to remove removing of sulfur component in the vinylbenzene that pyrolysis gasoline reclaims, and makes vinylbenzene to have obtained better technical effect as producing the cinnamic raw material of polymerization-grade.
Description of drawings
Fig. 1 is the process diagram that catalytic distillation removes Determination of Trace Sulfur in the vinylbenzene.
1 is catalytic rectifying tower among Fig. 1, and 2 is rectifying section, and 3 is conversion zone, and 4 is stripping section, and 5 is partial condenser, and 6 is reboiler, and 7 is sulfur-bearing vinylbenzene, and 8 is iso-butylene, and 9 is unreacted iso-butylene, and 10 are desulfurization vinylbenzene, and 11 for containing the vinylbenzene of heavy constituent sulphur.
By flow process shown in Figure 1; Sulfur-bearing vinylbenzene 7, iso-butylene 8 get into from the stripping section 4 and the tower still of catalytic rectifying tower 1 respectively; Sulphur component in the sulfur-bearing vinylbenzene 7 and iso-butylene 8 carry out alkylated reaction at conversion zone 3, generate heavy constituent sulphur, and heavy constituent sulphur is realized separating with stripping section 4 at rectifying section 2 with vinylbenzene; The unreacted iso-butylene 9 of dephlegmator of top of the tower 5 gas phase extraction; Liquid phase extraction desulfurization vinylbenzene 11, tower still part liquid phase is through reboiler 6 vaporizations, and a part obtains containing the vinylbenzene of heavy constituent sulphur as extraction.
Through specific embodiment the present invention is further described below, still, scope of the present invention has more than and is limited to the scope that embodiment covers.
Embodiment
[embodiment 1]
The number of theoretical plate of catalytic rectifying tower rectifying section is 10, the number of theoretical plate of stripping section is 10, the height of conversion zone is equivalent to the height of 5 theoretical stages, and catalyzer is the D001 macroporous ion exchange resin, and ion exchange resin ion kenel is the hydrogen radical ion; Sulfur-bearing vinylbenzene, iso-butylene get into from the 5th theoretical stage of catalytic rectifying tower stripping section (counting from top to bottom, as follows) and tower still respectively, and sulfur-bearing vinylbenzene flow is 30 gram/minute; Sulphur content is 150ppm, and the flow of iso-butylene is 5 ml/min, and reflux ratio is 6; Cat head liquid phase produced quantity is 27 gram/minute; Working pressure is 4KPa, and behind the stable operation, the cinnamic sulphur content of cat head desulfurization is 10ppm; The unreacted iso-butylene of gas phase extraction, the vinylbenzene that contains heavy constituent sulphur that the extraction of tower still obtains.
[embodiment 2]
The number of theoretical plate of catalytic rectifying tower rectifying section is 30, the number of theoretical plate of stripping section is 30, the height of conversion zone is equivalent to the height of 20 theoretical stages, and catalyzer is the ZSM-5 sieve catalyst, and silica alumina ratio is 45; Sulfur-bearing vinylbenzene, iso-butylene get into from the 10th theoretical stage of catalytic rectifying tower stripping section (counting from top to bottom, as follows) and tower still respectively, and sulfur-bearing vinylbenzene flow is 30 gram/minute; Sulphur content is 200ppm, and the flow of iso-butylene is 135 ml/min, and reflux ratio is 0.3; Cat head liquid phase produced quantity is 28.5 gram/minute; Working pressure is 20KPa, and behind the stable operation, the cinnamic sulphur content of cat head desulfurization is 4ppm; The unreacted iso-butylene of gas phase extraction, the vinylbenzene that contains heavy constituent sulphur that the extraction of tower still obtains.
[embodiment 3]
The number of theoretical plate of catalytic rectifying tower rectifying section is 15, the number of theoretical plate of stripping section is 20, the height of conversion zone is equivalent to the height of 10 theoretical stages, and catalyzer is the ZSM-5 sieve catalyst, and silica alumina ratio is 45; Sulfur-bearing vinylbenzene, iso-butylene get into from the 10th theoretical stage of catalytic rectifying tower stripping section (counting from top to bottom, as follows) and tower still respectively, and sulfur-bearing vinylbenzene flow is 30 gram/minute; Sulphur content is 180ppm, and the flow of iso-butylene is 45 ml/min, and reflux ratio is 1.2; Cat head liquid phase produced quantity is 28.5 gram/minute; Working pressure is 10KPa, and behind the stable operation, the cinnamic sulphur content of cat head desulfurization is 8ppm; The unreacted iso-butylene of gas phase extraction, the vinylbenzene that contains heavy constituent sulphur that the extraction of tower still obtains.
[embodiment 4]
The number of theoretical plate of catalytic rectifying tower rectifying section is 20, the number of theoretical plate of stripping section is 15, the height of conversion zone is equivalent to the height of 10 theoretical stages, and catalyzer is a Y type aluminium oxide catalyst, and silica alumina ratio is 30; Sulfur-bearing vinylbenzene, iso-butylene get into from the 8th theoretical stage of catalytic rectifying tower stripping section (counting from top to bottom, as follows) and tower still respectively, and sulfur-bearing vinylbenzene flow is 30 gram/minute; Sulphur content is 180ppm, and the flow of iso-butylene is 65 ml/min, and reflux ratio is 1.2; Cat head liquid phase produced quantity is 28.4 gram/minute; Working pressure is 10KPa, and behind the stable operation, the cinnamic sulphur content of cat head desulfurization is 2ppm; The unreacted iso-butylene of gas phase extraction, the vinylbenzene that contains heavy constituent sulphur that the extraction of tower still obtains.
[embodiment 5]
The number of theoretical plate of catalytic rectifying tower rectifying section is 30, the number of theoretical plate of stripping section is 30, the height of conversion zone is equivalent to the height of 20 theoretical stages, and catalyzer is the ZSM-5 sieve catalyst, and silica alumina ratio is 45; Sulfur-bearing vinylbenzene, iso-butylene get into from the 10th theoretical stage of catalytic rectifying tower stripping section (counting from top to bottom, as follows) and tower still respectively, and sulfur-bearing vinylbenzene flow is 30 gram/minute; Sulphur content is 500ppm, and the flow of iso-butylene is 270 ml/min, and reflux ratio is 0.3; Cat head liquid phase produced quantity is 28.5 gram/minute; Working pressure is 15KPa, and behind the stable operation, the cinnamic sulphur content of cat head desulfurization is 9ppm; The unreacted iso-butylene of gas phase extraction, the vinylbenzene that contains heavy constituent sulphur that the extraction of tower still obtains.

Claims (3)

1. a catalytic distillation removes the method for Determination of Trace Sulfur in the vinylbenzene; It is characterized in that sulphur content is not more than the sulfur-bearing vinylbenzene of 500ppm, iso-butylene and at the bottom of the stripping section of catalytic rectifying tower and tower, gets into respectively; Sulfur component in the vinylbenzene and iso-butylene react the generation heavy constituent at conversion zone, and vinylbenzene is realized separating in catalytic rectifying tower with the heavy constituent of generation simultaneously, and cat head is provided with partial condenser; The unreacted iso-butylene of gas phase extraction; Liquid phase extraction desulfurization vinylbenzene, sulphur content≤10ppm, the tower still obtains containing the vinylbenzene of heavy constituent sulphur;
The theoretical number of plates of rectifying section of catalytic rectifying tower is 10~30, and the stripping section number of theoretical plate is 10~30, and the height of conversion zone is equivalent to the height of 5~20 theoretical stages; The sulfur component raw materials components mole ratio is 1~30 in iso-butylene and the styrene material, and reflux ratio is 0.3~6, and recovery ratio is 90~98%, and working pressure is 4~20KPa.
2. remove the method for Determination of Trace Sulfur in the vinylbenzene according to right 1 said catalytic distillation, it is characterized in that the sulfur component raw materials components mole ratio is 5~10 in iso-butylene and the styrene material, reflux ratio is 0.7~1.5, and recovery ratio is 92~95%, and working pressure is 8~12KPa.
3. remove the method for Determination of Trace Sulfur in the vinylbenzene according to right 1 said catalytic distillation, it is characterized in that the conversion zone catalyst filling is at least a in acidic ion exchange resin or the solid acid catalyst.
CN2008100431327A 2008-02-20 2008-02-20 Method for removing trace sulfur in styrene by catalytic rectification Active CN101514137B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2008100431327A CN101514137B (en) 2008-02-20 2008-02-20 Method for removing trace sulfur in styrene by catalytic rectification

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2008100431327A CN101514137B (en) 2008-02-20 2008-02-20 Method for removing trace sulfur in styrene by catalytic rectification

Publications (2)

Publication Number Publication Date
CN101514137A CN101514137A (en) 2009-08-26
CN101514137B true CN101514137B (en) 2012-11-14

Family

ID=41038771

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2008100431327A Active CN101514137B (en) 2008-02-20 2008-02-20 Method for removing trace sulfur in styrene by catalytic rectification

Country Status (1)

Country Link
CN (1) CN101514137B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105712848B (en) * 2016-03-23 2018-02-02 陆明全 A kind of methyl tertiary butyl ether(MTBE) desulfurizing agent and its application method
CN116023225A (en) * 2023-02-20 2023-04-28 天津科技大学 Method for removing thiophenic sulfur in styrene by catalytic alkylation
CN116396139B (en) * 2023-06-08 2023-08-18 新疆天利石化股份有限公司 Method for catalytic removal of thiophene aromatic heterocyclic sulfur compounds in styrene in fixed bed reactor

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1412279A (en) * 2001-10-20 2003-04-23 中国石化集团齐鲁石油化工公司 Petroleum hydrocarbon hydrogenation desulfurization catalytic distillation process and its catalytic distillation equipment
CN101062879A (en) * 2006-04-28 2007-10-31 北京石油化工学院 Coking benzene deep desulfuration purification method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1412279A (en) * 2001-10-20 2003-04-23 中国石化集团齐鲁石油化工公司 Petroleum hydrocarbon hydrogenation desulfurization catalytic distillation process and its catalytic distillation equipment
CN101062879A (en) * 2006-04-28 2007-10-31 北京石油化工学院 Coking benzene deep desulfuration purification method

Also Published As

Publication number Publication date
CN101514137A (en) 2009-08-26

Similar Documents

Publication Publication Date Title
CN102372573B (en) Method for preparing propylene by using etherified C4 and ethylene
CN101062879B (en) Coking benzene deep desulfuration purification method
CN100593531C (en) Method for reclaiming and purifying styrene
CN101492360B (en) Process for the separation of aqueous phase by-product of fischer-tropsch synthesis reaction
CN105152840A (en) Process for refining C-4 hydrocarbon fluid
CN101885660B (en) C4 hydrocarbon catalysis and separation method capable of separating isobutene and butene-2
CN101475438A (en) Selective hydrogenation method for phenylacetylene in the presence of phenylethylene
CN101544532B (en) Method for producing butylene-1 by utilizing catalytic cracking by-product C4 hydrocarbons and ethylene cracking by-product C4 hydrocarbons as raw materials
CN101597510A (en) A kind of catalytic distillation method of alkylation desulfurization of gasoline
CN103865562A (en) Method for preparing gasoline from methanol
CN101514137B (en) Method for removing trace sulfur in styrene by catalytic rectification
CN102372600A (en) Separation method for glycol, propylene glycol and butylene glycol
CN103992832A (en) Method for refining liquefied petroleum gas
CN101152994A (en) Method for refining carbonization crude benzole
CN102190555A (en) Method for recovering styrene
CN115772061B (en) Method for catalytic removal of thiophenic sulfur compounds in styrene
CN101429090B (en) Decolorization method for recycling vinyl benzene with pyrolysis gasoline
CN116023225A (en) Method for removing thiophenic sulfur in styrene by catalytic alkylation
CN101475437B (en) Method for removing phenylacetylene in the presence of phenylethylene
CN101362671B (en) Method for preparing polymer grade 1-butene by high sulfur content four carbon compounds catalysis from refinery
CN102649678A (en) Method for removing phenylacetylene through highly selective hydrogenation in presence of styrene
CN101993327B (en) Process of carrying out reaction, rectifying and coupling to selectively hydrogenate to remove MAPD (Methylacetylene Propadiene)
CN101987970B (en) Method for removing mercaptan from gasoline
CN101597024B (en) Method for producing hydrogen with refinery dry gas
CN101962311B (en) Method and device for increasing service life of extractant in hydrofining process of crude benzene

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant