GB520255A - Separation of polymerisable organic compounds - Google Patents

Separation of polymerisable organic compounds

Info

Publication number
GB520255A
GB520255A GB30069/38A GB3006938A GB520255A GB 520255 A GB520255 A GB 520255A GB 30069/38 A GB30069/38 A GB 30069/38A GB 3006938 A GB3006938 A GB 3006938A GB 520255 A GB520255 A GB 520255A
Authority
GB
United Kingdom
Prior art keywords
mva
acetylene
column
condenser
returned
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.)
Expired
Application number
GB30069/38A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB520255A publication Critical patent/GB520255A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Analytical Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Water Supply & Treatment (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

520,255. Recovering volatile liquids. DU PONT DE NEMOURS & CO., E. I. Oct. 17, 1938, No. 30069. Convention date, Oct. 15, 1937. [Class 32] [Also in Group IV] Volatile constituents are separated from a liquid composition containing a heat-polymerizable unsaturated organic compound by bringing an inert gas into contact with said composition to entrain the volatile constituents, the temperature being maintained below that at which the polymerizable compound is polymerized in substantial amount (1.5 per cent.), and separating the gas with entrained constituents from the liquid. The invention is particularly applicable to the separation of monofrom divinylacetylene, of divinylacetylene from an oily acetone-soluble polymer thereof, and of vinylacetylene from its hydrogen halide addition products. Two or more stripping columns may be used, the liquid composition passing down through these in series against an upward current of inert gas, the entrained volatile constituents being condensed out from the gas leaving each column. A liquid composition containing 10-15 per cent. oily divinylacetylene polymers, 80-85 divinylacetylene, and 5 per cent. xylene may be treated using nitrogen as inert gas and a stripping temperature of 20-45‹C. The columns may contain close fitting spirals to distribute the liquids over the walls or may be plain or packed. Hydrogen, carbon dioxide and the inert gases of Group O may also be used. Pressure is usually normal or slightly above. In the polymerization of acetylene to give mainly mono- or di-vinylacetylene, acetylene is fed to reactor 1, Fig. 2, which may contain aqueous cuprous and ammonium chlorides at 45-100‹C. The exit gases pass to 0‹C. condenser 4, water separating as the bottom layer in separator 5 and being returned to the reactor. A second liquid layer rich in divinylacetylene (DVA) generally forms and is drawn off at 9 and passed to stripping column 21. A gaseous mixture of acetylene and monovinylacetylene (MVA) leaves at 10 and, where MVA is the desired product, passes to -65 to -75‹C. condenser 11, acetylene being vented at 13 and recycled, and the condensed MVA containing some DVA passing to column 17 which is at 18-25‹C. MVA is vented at 18 and the residual crude DVA is fed to stripping column 21 where it meets an upward current of acetylene which entrains MVA. The gases are returned to the system at 28 and DVA leaves the column at 29. When DVA is the main product, the acetylene and MVA leaving at 10 are returned direct by valve 30 to the reactor 1. Examples are given. In the production of chloroprene from vinylacetylene, the latter may be stripped from the product using acetylene, advantageously at 20-45‹C. Acetylene is polymerized in reactor 2, Fig. 3, water is removed from the products in drier 3, acetylene removed in 5 and 7, and the monovinylacetylene vaporized in 13. It is fed to reactor 16 and reacted with hydrogen chloride, the product containing chloroprene (CD) being liquefied in condenser 20 and fed to a column 21 at 30-35‹C. Part of the MVA is vaporized and returned by pipe 23. The liquid passes to a stripping column 25 where acetylene entering at 29 entrains MVA and is returned via reflux condenser 31 and lines 32, 34. Chloroprene leaves at 36. Other inert gases may be used in the stripping stage. Thus nitrogen may be introduced into column 25 at 37, the exit gases passing by line 32 and valve 33 to a condenser 39 where nitrogen and MVA are separated and returned. The reflux condenser 31 may be omitted allowing some chloroprene to be stripped with the MVA. The two are condensed in 39 and added to the condensate from condenser 20 at 44. Other hydrogen chloride or bromide addition products may be prepared similarly.
GB30069/38A 1937-10-15 1938-10-17 Separation of polymerisable organic compounds Expired GB520255A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US520255XA 1937-10-15 1937-10-15

Publications (1)

Publication Number Publication Date
GB520255A true GB520255A (en) 1940-04-18

Family

ID=21974932

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30069/38A Expired GB520255A (en) 1937-10-15 1938-10-17 Separation of polymerisable organic compounds

Country Status (1)

Country Link
GB (1) GB520255A (en)

Similar Documents

Publication Publication Date Title
US2714940A (en) Purification of acetylenes
US1422183A (en) Process of treating gaseous mixtures
US2161798A (en) Chemical process
ES363604A2 (en) Separation of acetylene and ethylene from cracked gas
US3365375A (en) Process for separating decomposition products of cumene hydroperoxide
US2303609A (en) Crude oil conditioning and separating process
US3293869A (en) Gas liquefaction with recombining of separated gas-liquid fractions
US3925047A (en) Removal of moisture from a natural gas stream by contacting with a liquid desiccant-antifreeze agent and subsequently chilling
GB520255A (en) Separation of polymerisable organic compounds
US2384378A (en) Separation of sulphur dioxide and low-boiling hydrocarbons from mixtures thereof
US3496069A (en) Purification of unsaturated hydrocarbons by extractive distillation with recycle of stripper overhead
GB1508248A (en) Recovery of hydrogen chloride from gaseous product streams containing chlorinated hydrocarbons such as chloromethanes
US2356986A (en) Process for separating hydrocarbons
US1231123A (en) Production of chlorinated hydrocarbons.
US2596692A (en) Method of absorbing gases, including hydrogen sulfide
US2207784A (en) Process for making 2-chloro-1,3-butadiene
US2403977A (en) Dichlorides of the ethylene series
US2753012A (en) Process for separating acetylenic components from mixtures
BR112013026711B1 (en) monomer recovery
US3236029A (en) Recovery of hydrocarbons
US2914589A (en) Control of oxygen content of low boiling hydrocarbons
US7445702B2 (en) Desulphurisation
JPS6230173B2 (en)
EP0027805B1 (en) Improved process for removal and recovery of vinyl chloride monomer from vent gas stream in polyvinyl chloride plant
US3213154A (en) Hydrocarbon treating