CN102432426A - Method for separating and purifying dichloropropane and dichloropropylene - Google Patents

Method for separating and purifying dichloropropane and dichloropropylene Download PDF

Info

Publication number
CN102432426A
CN102432426A CN201110415024XA CN201110415024A CN102432426A CN 102432426 A CN102432426 A CN 102432426A CN 201110415024X A CN201110415024X A CN 201110415024XA CN 201110415024 A CN201110415024 A CN 201110415024A CN 102432426 A CN102432426 A CN 102432426A
Authority
CN
China
Prior art keywords
dichloropropylene
rectifying tower
rectifying
tower
extraction
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.)
Granted
Application number
CN201110415024XA
Other languages
Chinese (zh)
Other versions
CN102432426B (en
Inventor
项曙光
孙晓岩
夏力
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.)
Qingdao University of Science and Technology
Original Assignee
Qingdao University of Science and 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 Qingdao University of Science and Technology filed Critical Qingdao University of Science and Technology
Priority to CN201110415024.XA priority Critical patent/CN102432426B/en
Publication of CN102432426A publication Critical patent/CN102432426A/en
Application granted granted Critical
Publication of CN102432426B publication Critical patent/CN102432426B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention belongs to the technical field of separation and purification of chemical substances, and relates to a method for separating and purifying dichloropropane and dichloropropylene by Dorlone, particularly a method for separating and purifying dichloropropane and dichloropropylene from a byproduct Dorlone discharged from a rectification tower in a propylene high-temperature chlorination production process. The method can effectively utilize the Dorlone, and comprises the steps of 1,2-dichloropropane rectification, high-boiling substance separation, 3,3-dichloropropylene separation and 1,3-dichloropropylene separation. By using the method, the recovery rate of the 1,2-dichloropropane is up to more than 80%, the recovery rate of the 1,3-dichloropropylene is up to more than 90%, the two cis-trans-isomers of the 1,3-dichloropropylene can be well separated, the purity of the recovered products 1,2-dichloropropane and 1,3-dichloropropylene is up to more than 99%, and thus, the method has high economic benefit; and the invention has the advantages of simple overall technique, high separation and purification efficiency, good quality and production environment friendliness.

Description

The separation purification method of a kind of propylene dichloride and dichloropropylene
Technical field:
The invention belongs to chemical substance separates and the purification technique field; Relate to a kind of method by D-D mixture separation and purification propylene dichloride and dichloropropylene; Particularly a kind of in propylene high-temperature chlorination production process from the by product D-D mixture that rectifying tower is discharged the method for separation and purification propylene dichloride and dichloropropylene, can effectively utilize the D-D mixture.
Background technology:
Along with China's production of propylene oxide ability strengthens year by year; Produce the by product D-D mixture that produces in the 3-vinylchlorid process in acrylonitrile-chlorinated method also increases thereupon, contain in the D-D mixture a large amount of 1,2-propylene dichloride, 3; 3-dichloropropylene, 1,3-dichloropropylene and a spot of high boiling material.Because the D-D mixture has nematicide medicament and herbicide action, all be widely used at world wide, be 1 as the staple of agricultural chemicals, the 3-dichloropropylene, a large amount of 1, the 2-propylene dichloride is dispersed in soil and the air, can cause serious pollution to environment; 1, the 2-propylene dichloride can be used for preparing paint, printing ink, thinner and PVC sizing agent as a kind of good organic solvent.Present domestic processing D-D mixture generally is directly to use as paint thinner or agricultural chemicals after the process simple distillation, also has part D-D mixture directly as the boiler oil burning disposal, and this is the root that produces the three wastes, has promptly wasted resource and has also polluted environment.Have report can adopt rectification method with 1,3-dichloropropylene cut purity is increased to more than 90%, is used for the synthetic of agricultural chemicals or other fine-chemical intermediate; The somebody attempts to adopt rectification method with 1 in the D-D mixture, 3-dichloropropylene and 1, and the 2-propylene dichloride separates; But because the component boiling point is close; Be difficult to the warp separation fully of each component is decomposited HCl after the D-D mixture is heated, the column efficiency and the erosion resistance of rectifier unit are had higher requirement.Therefore, reasonable development goes out the approach of effective D-D mixture comprehensive utilization, therefrom isolate respectively purity higher 1,3-dichloropropylene and 1, the 2-propylene dichloride has important environment protection significance and economic benefit.
Summary of the invention:
The objective of the invention is to overcome the shortcoming that prior art exists, seek to provide a kind of by the by product D-D mixture separation and purification propylene dichloride that produces in the propylene high-temperature chlorination reaction process and the technical process of dichloropropylene, to 1; The 2-propylene dichloride recovery reaches more than 80%, and to 1, the 3-dichloropropylene recovery reaches more than 90%; And can be with 1; Two kinds of cis-trans-isomers that the 3-dichloropropylene exists separate 1 of recovery, 2-propylene dichloride and 1 preferably; 3-dichloropropylene product gas purity can reach more than 99%, has high economic benefit.
To achieve these goals, the inventive method comprises 1,2 propylene dichloride rectifying, high boiling material separation, 3,3-dichloropropylene separation and 1; The 3-dichloropropylene separates four steps, will contain 1,2 propylene dichloride, 3 earlier, 3-dichloropropylene, cis 1; 3-dichloropropylene, trans 1, the D-D mixture raw material of 3-dichloropropylene, trieline and trichloroethane gets into first rectifying tower through the pressure pump back of boosting, and the first rectifying tower cat head is provided with condensing surface, and the pressure of being controlled first rectifying tower by vacuum pump is lower than 80kPa; Temperature is controlled at below 80 ℃, and the tower still is provided with reboiler, and the temperature of reboiler is controlled at below 140 ℃; D-D mixture raw material through the first rectifying tower rectifying after, vapour phase gets into drainer by the rectifying tower top extraction after condensation; Partial reflux, it is subsequent use that all the other get into drainer as product 1,2 propylene dichloride extraction; After the separation of first rectifying tower, 1 more than 99%, the 2-propylene dichloride is recovered; The surplus materials raw material is squeezed into second rectifying tower by pressure pump after by the first rectifier bottoms extraction and is carried out rectifying, and the second rectifying tower cat head is provided with condensing surface, and the pressure of being controlled second rectifying tower by vacuum pump is lower than 90kPa; Temperature is controlled at below 90 ℃, and the tower still is provided with reboiler, and its temperature is controlled at below 150 ℃; The surplus materials raw material through second rectifying tower after, liquid phase by the tower of second rectifying tower at the bottom of extraction, high boiling material is separated from blending ingredients; Get into the waste oil storage tank as waste oil, vapour phase gets into drainer by the cat head extraction of second rectifying tower after condensation; Partial reflux gets into the 3rd rectifying tower after the extraction of remaining mixture material; Comprise 3 in the mixture of the cat head extraction of second rectifying tower; 3-dichloropropylene, cis and trans 1, the 3-dichloropropylene, the mixture that will comprise above-mentioned three kinds of components is squeezed into the 3rd rectifying tower by pressure pump; The 3rd rectifying Tata still is provided with reboiler; Its temperature is controlled at below 140 ℃, and tower top temperature is controlled at below 120 ℃, and pressure is 102-160kPa; Mixture through the 3rd rectifying tower rectifying after, vapour phase gets into drainer at cat head after the water cooler condensation, partial reflux, remaining mixture material be as 3, the extraction of 3-dichloropropylene product gets into storage tank; Liquid phase by tower at the bottom of extraction, squeeze in the 4th rectifying tower subsequent use by pressure pump; The material of extraction comprises cis and trans 1 at the bottom of the 3rd rectifying Tata; The 3-dichloropropylene, the mixture that will comprise above-mentioned two kinds of components is squeezed in the 4th rectifying tower by pressure pump, and the 4th rectifying Tata still is provided with reboiler; Temperature is controlled at below 100 ℃; Cat head is provided with vacuum pump, and its temperature is controlled at below 60 ℃, and pressure is lower than 25kPa; Mixture through the 4th rectifying tower rectifying after, vapour phase gets into drainer at cat head after the water cooler condensation, partial reflux, rest materials is as trans 1, the extraction of 3-dichloropropylene product gets into storage tank; Liquid phase extracts as cis 1 at the bottom of by the tower of the 4th rectifying tower, and it is subsequent use that 3-dichloropropylene product gets into storage tank stores.
The present invention compared with prior art according to the nature difference of each component of material, carries out comprehensively the rectifying tower that is used to separate different components; And the means that adopt decompression technology and supercharging technology to combine, can realize separation and purification efficiently 1,2-propylene dichloride and 1; The 3-dichloropropylene is removed high boiling material, preserves the ecological environment; Economize on resources again, accomplish to make the best use of everything, reduce the financial loss in producing; Its overall craft process is simple, and condition control is convenient, and product goes out the rate height, quality better, and production environment is friendly, the conservation resource, economic worth is high, and social benefit is good.
Description of drawings:
Fig. 1 is that equipment of the present invention is formed structure and technical process principle schematic.
Embodiment:
Below through embodiment and combine accompanying drawing to be described further.
Present embodiment will contain 1,2 propylene dichloride, 3 earlier, 3-dichloropropylene, cis 1; 3-dichloropropylene, trans 1, the D-D mixture raw material of 3-dichloropropylene, trieline and trichloroethane gets into the first rectifying tower T101 through the pressure pump P101 back of boosting, and the first rectifying tower cat head is provided with condensing surface E102; The pressure of being controlled first rectifying tower by vacuum pump P200 is lower than 80kPa, and temperature is controlled at below 80 ℃, and the tower still is provided with reboiler E101; The temperature of reboiler is controlled at below 140 ℃, D-D mixture raw material through the first rectifying tower T101 rectifying after, vapour phase is by the rectifying tower top extraction; After condensation, get into drainer U100; Partial reflux, it is subsequent use that all the other get into the U200 drainer as product 1,2 propylene dichloride extraction; After first rectifying tower T101 separation, 1 more than 99%, the 2-propylene dichloride is recovered; The surplus materials raw material is squeezed into the second rectifying tower T102 by pressure pump P103 after the extraction and is carried out rectifying bottom the first rectifying tower T101, the second rectifying tower T102 cat head is provided with condensing surface E103, and the pressure of being controlled the second rectifying tower T102 by vacuum pump P201 is lower than 90kPa; Temperature is controlled at below 90 ℃, and the tower still is provided with reboiler E104, and its temperature is controlled at below 150 ℃; The surplus materials raw material through the second rectifying tower T102 after, liquid phase by the tower of the second rectifying tower T102 at the bottom of extraction, high boiling material is separated from blending ingredients; Get into waste oil storage tank U101 as waste oil, vapour phase gets into drainer U102 by the cat head extraction of the second rectifying tower T102 after condensation; Partial reflux gets into the 3rd rectifying tower T103 after the extraction of remaining mixture material; Comprise 3 in the mixture of the cat head extraction of the second rectifying tower T102; 3-dichloropropylene, cis and trans 1, the 3-dichloropropylene, the mixture that will comprise above-mentioned three kinds of components is squeezed into the 3rd rectifying tower T103 by pressure pump; The 3rd rectifying tower T103 tower still is provided with reboiler E105; Go temperature to be controlled at below 140 ℃, tower top temperature is controlled at below 120 ℃, and pressure is 102-160kPa; Mixture through the 3rd rectifying tower T103 rectifying after, vapour phase gets into drainer U103 at cat head after water cooler E106 condensation, partial reflux, remaining mixture material be as 3, the extraction of 3-dichloropropylene product gets into storage tank U104; Liquid phase by tower at the bottom of extraction, squeeze among the 4th rectifying tower T104 subsequent use by pressure pump P106; The material of extraction comprises cis and trans 1 at the bottom of the 3rd rectifying tower T103 tower; The 3-dichloropropylene, the mixture that will comprise above-mentioned two kinds of components is squeezed among the 4th rectifying tower T104 by pressure pump, and the 4th rectifying tower T104 tower still is provided with reboiler E107; Temperature is controlled at below 100 ℃; Cat head is provided with vacuum pump P202, and temperature is controlled at below 60 ℃, and pressure is lower than 25kPa; Mixture through the 4th rectifying tower T104 rectifying after, vapour phase gets into drainer U105 at cat head after water cooler E108 condensation, partial reflux, rest materials is as trans 1, the extraction of 3-dichloropropylene product gets into storage tank U106; Liquid phase extracts as cis 1 at the bottom of by the tower of the 4th rectifying tower T104, and 3-dichloropropylene product gets into storage tank U107 and stores for future use.
Embodiment 1:
Present embodiment is through heat and material balance to the technical process of D-D mixture separation and purification process, and the operating mode of 40,000 tons of D-D mixtures year is handled in simulation, will comprise mass content and be 82.1% 1; The 2-propylene dichloride, 0.6% 3,3-dichloropropylene, 5.3% cis 1, the 3-dichloropropylene, 10.8% trans 1; The D-D mixture raw material of 3-dichloropropylene and 1.1% high boiling material is squeezed into the first rectifying tower T101 with the 4600kg/hr flow by pressure pump P101, and the first rectifying tower T101 cat head is established condensing surface E100, is 40kPa by vacuum pump P200 control tower top pressure; Temperature is controlled at 67 ℃, and the tower still is established reboiler E101, and temperature is controlled at 118 ℃; Raw material through first rectifying tower after, vapour phase is by the cat head extraction, after condensation, gets into drainer U100; Part is refluxed by pump P102; All the other are as product 1,2 propylene dichloride extraction to product jar U200, and product purity is 99.8%;
After the separation of first rectifying tower, 1 more than 99%, the 2-propylene dichloride is recovered; All the other materials are squeezed into the second rectifying tower T102 by pressure pump P103 after the extraction at the bottom of by tower; The second rectifying tower cat head is established condensing surface E103, is 40kPa by vacuum pump P201 control tower top pressure, and temperature is controlled at 77 ℃; The tower still is established reboiler E104, and temperature is controlled at 131 ℃; Raw material through the second rectifying tower T102 after; Liquid phase by tower at the bottom of extraction, high boiling material is separated from blending ingredients, by pressure pump P104 as among the waste oil input waste oil storage tank U101; Vapour phase is by the cat head extraction; After condensation, get into drainer U102, part refluxes via pressure pump P105, gets into the 3rd rectifying tower T103 after all the other extraction; After second rectifying tower T102 separation, all high boiling material separate cat head mass flow of materials 760kg/hr at the bottom of tower; Wherein 3,3 dichloropropylene content are 3.1%, 1; 2-propylene dichloride content is 0.6%; Cis 1,3-dichloropropylene content be 30.8% and 65.5% trans 1, the 3-dichloropropylene;
The second rectifying tower cat head production mainly comprises 3,3-dichloropropylene and cis, trans 1,3-dichloropropylene and a spot of 1,2-propylene dichloride; The partial confounding compound is squeezed among the 3rd rectifying tower T103 by pressure pump P105, and the 3rd rectifying Tata still is established reboiler E105, and temperature is controlled at 131 ℃, and tower top temperature is controlled to be 113 ℃; Pressure 152kPa, mixture through the 3rd rectifying tower T103 after, vapour phase gets into drainer U103 at cat head after water cooler E106 condensation; Part is refluxed by pressure pump P107, and all the other contain 3,3-dichloropropylene, cis and trans 1; 3-dichloropropylene mixture gets into a jar U104 by the cat head extraction, and wherein 3,3-dichloropropylene concentration is 73.5%; Liquid phase by tower at the bottom of extraction, the production mass rate is 728kg/hr, wherein cis 1,3-dichloropropylene content 32.2% is trans 1,3-dichloropropylene content 67.8%, this mixture is squeezed among the 4th rectifying tower T104 subsequent use by pressure pump P106;
Production mainly comprises cis and trans 1,3-dichloropropylene at the bottom of the 3rd rectifying Tata.The mixture that will comprise these two kinds of components is squeezed among the 4th rectifying tower T104 by pressure pump P103, and the tower still of the 4th rectifying tower T104 is established reboiler E107, and temperature is controlled at 90 ℃; Cat head is established vacuum pump P202, and temperature is controlled at 47 ℃, pressure 13.3kPa; Raw material through the 4th rectifying tower T104 rectifying after, vapour phase gets into drainer U105 at cat head after water cooler E108 condensation, part is refluxed by pressure pump P108, all the other are as trans 1, the extraction of 3-dichloropropylene product gets among the storage tank U106, purity is 99.9%; Liquid phase by tower at the bottom of as cis 1,3-dichloropropylene product is got among the storage tank U107 by pressure pump P109 extraction, purity is 99.9%.
Present embodiment is according to the nature difference of each component, the rectifying tower that is used to separate different components carried out comprehensively, and the means that adopt decompression technology and supercharging technology to combine; Remove 3,3-dichloropropylene and high boiling material are realized separation and purification efficiently 1; 2-propylene dichloride and 1,3-dichloropropylene, product 1; 2-propylene dichloride and cis, trans 1,3-dichloropropylene purity all reaches more than 99%.

Claims (1)

1. the separation purification method of propylene dichloride and dichloropropylene, it is characterized in that comprising 1,2 propylene dichloride rectifying, high boiling material separate, 3, the 3-dichloropropylene separates and 1; The 3-dichloropropylene separates four steps, and 1,2 propylene dichloride rectification process is: will contain 1 earlier; 2 propylene dichlorides, 3,3-dichloropropylene, cis 1,3-dichloropropylene, trans 1; The D-D mixture raw material of 3-dichloropropylene, trieline and trichloroethane gets into first rectifying tower after boosting through pressure pump, and the first rectifying tower cat head is provided with condensing surface, and the pressure of being controlled first rectifying tower by vacuum pump is lower than 80kPa; Temperature is controlled at below 80 ℃, and the tower still is provided with reboiler, and the temperature of reboiler is controlled at below 140 ℃; D-D mixture raw material through the first rectifying tower rectifying after, vapour phase gets into drainer by the rectifying tower top extraction after condensation; Partial reflux, it is subsequent use that all the other get into drainer as product 1,2 propylene dichloride extraction; The high boiling material separating technology is: after separating through first rectifying tower, and 1 more than 99%, the 2-propylene dichloride is recovered; The surplus materials raw material is squeezed into second rectifying tower by pressure pump after by the first rectifier bottoms extraction and is carried out rectifying, and the second rectifying tower cat head is provided with condensing surface, and the pressure of being controlled second rectifying tower by vacuum pump is lower than 90kPa; Temperature is controlled at below 90 ℃, and the tower still is provided with reboiler, and its temperature is controlled at below 150 ℃; The surplus materials raw material through second rectifying tower after, liquid phase by the tower of second rectifying tower at the bottom of extraction, high boiling material is separated from blending ingredients; Get into the waste oil storage tank as waste oil, vapour phase gets into drainer by the cat head extraction of second rectifying tower after condensation; Partial reflux gets into the 3rd rectifying tower after the extraction of remaining mixture material; 3,3-dichloropropylene separating technology is: comprise 3 in the mixture of the cat head extraction of second rectifying tower, 3-dichloropropylene, cis and trans 1; The 3-dichloropropylene; The mixture that will comprise above-mentioned three kinds of components is squeezed into the 3rd rectifying tower by pressure pump, and the 3rd rectifying Tata still is provided with reboiler, and its temperature is controlled at below 140 ℃; Tower top temperature is controlled at below 120 ℃, and pressure is 102-160kPa; Mixture through the 3rd rectifying tower rectifying after, vapour phase gets into drainer at cat head after the water cooler condensation, partial reflux, remaining mixture material be as 3, the extraction of 3-dichloropropylene product gets into storage tank; Liquid phase by tower at the bottom of extraction, squeeze in the 4th rectifying tower subsequent use by pressure pump; 1,3-dichloropropylene separating technology is: the material of extraction comprises cis and trans 1,3-dichloropropylene at the bottom of the 3rd rectifying Tata; The mixture that will comprise above-mentioned two kinds of components is squeezed in the 4th rectifying tower by pressure pump; The 4th rectifying Tata still is provided with reboiler, and temperature is controlled at below 100 ℃, and cat head is provided with vacuum pump; Its temperature is controlled at below 60 ℃, and pressure is lower than 25kPa; Mixture through the 4th rectifying tower rectifying after, vapour phase gets into drainer at cat head after the water cooler condensation, partial reflux, rest materials is as trans 1, the extraction of 3-dichloropropylene product gets into storage tank; Liquid phase extracts as cis 1 at the bottom of by the tower of the 4th rectifying tower, and it is subsequent use that 3-dichloropropylene product gets into storage tank stores.
CN201110415024.XA 2011-12-14 2011-12-14 Method for separating and purifying dichloropropane and dichloropropylene Active CN102432426B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201110415024.XA CN102432426B (en) 2011-12-14 2011-12-14 Method for separating and purifying dichloropropane and dichloropropylene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201110415024.XA CN102432426B (en) 2011-12-14 2011-12-14 Method for separating and purifying dichloropropane and dichloropropylene

Publications (2)

Publication Number Publication Date
CN102432426A true CN102432426A (en) 2012-05-02
CN102432426B CN102432426B (en) 2013-11-06

Family

ID=45980822

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201110415024.XA Active CN102432426B (en) 2011-12-14 2011-12-14 Method for separating and purifying dichloropropane and dichloropropylene

Country Status (1)

Country Link
CN (1) CN102432426B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104387226A (en) * 2014-11-20 2015-03-04 闾正军 Purification method of dichloropropene
CN107879891A (en) * 2017-11-20 2018-04-06 天津辰力工程设计有限公司 A kind of method that dichloropropane and dichloropropylene are purified using DD mixtures
CN111807925A (en) * 2020-07-23 2020-10-23 山东海益化工科技有限公司 D-D mixture rectification separation process
CN111848334A (en) * 2020-07-30 2020-10-30 江苏扬农化工集团有限公司 Method for treating by-products in process of preparing chloropropene by chlorination of propylene

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1231127A (en) * 1968-12-18 1971-05-12
US3634200A (en) * 1969-02-20 1972-01-11 Stauffer Chemical Co Ethylene dichloride purification by plural stage distillation
CN1282724A (en) * 1999-07-31 2001-02-07 崔英武 Process for extracting dichloropropene from D-D mixture
CN1847205A (en) * 2005-03-31 2006-10-18 沈阳化工学院 Method of separating 1,2-dichloropropane with DD mixture

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1231127A (en) * 1968-12-18 1971-05-12
US3634200A (en) * 1969-02-20 1972-01-11 Stauffer Chemical Co Ethylene dichloride purification by plural stage distillation
CN1282724A (en) * 1999-07-31 2001-02-07 崔英武 Process for extracting dichloropropene from D-D mixture
CN1847205A (en) * 2005-03-31 2006-10-18 沈阳化工学院 Method of separating 1,2-dichloropropane with DD mixture

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104387226A (en) * 2014-11-20 2015-03-04 闾正军 Purification method of dichloropropene
CN104387226B (en) * 2014-11-20 2017-05-17 闾正军 Purification method of dichloropropene
CN107879891A (en) * 2017-11-20 2018-04-06 天津辰力工程设计有限公司 A kind of method that dichloropropane and dichloropropylene are purified using DD mixtures
CN107879891B (en) * 2017-11-20 2020-09-29 天津辰力工程设计有限公司 Method for purifying dichloropropane and dichloropropene by using DD (DD) mixing agent
CN111807925A (en) * 2020-07-23 2020-10-23 山东海益化工科技有限公司 D-D mixture rectification separation process
CN111807925B (en) * 2020-07-23 2021-11-02 山东海益化工科技有限公司 D-D mixture rectification separation process
WO2022016631A1 (en) * 2020-07-23 2022-01-27 山东海益化工科技有限公司 Rectification separation process for d-d mixture
CN111848334A (en) * 2020-07-30 2020-10-30 江苏扬农化工集团有限公司 Method for treating by-products in process of preparing chloropropene by chlorination of propylene

Also Published As

Publication number Publication date
CN102432426B (en) 2013-11-06

Similar Documents

Publication Publication Date Title
CN102432426B (en) Method for separating and purifying dichloropropane and dichloropropylene
MX2012000608A (en) Recovery of butanol from a mixture of butanol, water and an organic extractant.
MX2012000616A (en) Recovery of butanol from a mixture of butanol, water and an organic extractant.
CN104926587A (en) Energy-saving process flow of 1-butene separation purification
CN101973845B (en) Method for extracting butyraldehyde and butanol mixture and octenal and octanol mixture from waste liquid discharged by butanol-octanol device
CN109912500B (en) Method and device for refining high-purity pyridine series products from crude pyridine
CN102766016A (en) Method for recovering octafluoropropane from hexafluoropropylene production process
CN102584544B (en) Process for separating ethylene glycol monomethyl ether and water with intermittent azeotropic distillation method
CN102627556B (en) Technology of extractive distillation separation of ethyl acetate-ethanol-water
CN110066226B (en) Refining process of acetonitrile-containing wastewater
CN105949061A (en) Process and device for recycling dimethyl carbonate through steam permeation method
CN101260016A (en) Refining device for preparing high-pure isobutene by cracking methyl tertiary butyl ether and technique thereof
CN101229471A (en) Toluol-benzene solvent recovery technology from vent gas
CN102531834A (en) System and process for recovering waste liquid in 1, 4-butanediol production process
CN104961624B (en) Octyl alconyl produces the recoverying and utilizing method of waste liquid
CN110668910B (en) Benzene distillation residue recovery device, recovery method and application
CN106349107A (en) Method and device for separating acetonitrile-triethylamine mixture through heterogeneous azeotropic rectification
CN108358808B (en) Method for recovering dimethylacetamide in waste oil of cyclohexanone device
CN116410068A (en) Method for separating methyl tertiary butyl ether-ethanol-water mixture by extractive distillation
CN115340443A (en) Method for separating isopropanol-water-ethanol mixture by thermal coupling extractive distillation
CN104130095A (en) Cis-decahydronaphthalene and trans-decahydronaphthalene separating method
CN106866369A (en) A kind of separation method of polyol blends
CN206799475U (en) A kind of purifying plant of the recovery of acetic acid from acetic acid wastewater
TW202112721A (en) Method for purifying by-product ethylene glycol of polyester in converting plasticizer
CN114890861B (en) Extractive distillation method for separating mixture of n-propyl acetate and methylcyclohexane by using polyalcohol

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