GB343116A - Manufacture of oily polymerisation products from butadiene or a homologue thereof - Google Patents

Manufacture of oily polymerisation products from butadiene or a homologue thereof

Info

Publication number
GB343116A
GB343116A GB31454/29A GB3145429A GB343116A GB 343116 A GB343116 A GB 343116A GB 31454/29 A GB31454/29 A GB 31454/29A GB 3145429 A GB3145429 A GB 3145429A GB 343116 A GB343116 A GB 343116A
Authority
GB
United Kingdom
Prior art keywords
butadiene
passed
iron
vinylcyclohexenes
aluminium
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
GB31454/29A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB343116A publication Critical patent/GB343116A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F36/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F36/02Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F36/04Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F136/00Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F136/02Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F136/04Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated

Abstract

Oily polymerization products of butadiene and its homologues are produced by heating the initial hydrocarbon to about 400 DEG C. or higher at ordinary pressure, with or without a catalyst. In the Examples (1) butadiene is passed through an iron tube filled with iron turnings at 400-500 DEG C., the issuing vapours being passed into a condenser preferably at 50 DEG C. when an oil mainly consisting of vinylcyclohexenes boiling at 110-135 DEG C. condenses; instead of iron, other metals such as aluminium, copper, or nickel may be used, also nonmetallic catalysts: (2) butadiene is passed over nickel supported on pumice at 400-500 DEG C., the greater part of the condensate being vinylcyclohexenes, but a fraction boils above 200 DEG C., especially when the speed is low and the temperature about 500 DEG C.: (3) butadiene is passed through an aluminium tube containing aluminium splinters, yielding vinylcyclohexenes: (4) butadiene is passed in a strong current through a glass tube filled with glass wool at 430-450 DEG C.: (5) butadiene is passed slowly at 430-450 DEG C. through a porcelain tube containing silica gel: (6) isoprene is passed through a glass tube containing glass wool at 400-430 DEG C., the condensate boiling principally between 165 DEG C. and 180 DEG C. and probably containing dipentene: (7) 1,3 dimethyl butadiene obtained by eliminating water from methyl pentandiol is passed through an iron tube containing iron sponge (from iron carbonyl) at 400 DEG C., the condensate boiling at 195-210 DEG C., or at 13 mm., at 90-100 DEG C. In all cases the unchanged diolefine is separated and returned to the tube.
GB31454/29A 1928-10-16 1929-10-16 Manufacture of oily polymerisation products from butadiene or a homologue thereof Expired GB343116A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE343116X 1928-10-16

Publications (1)

Publication Number Publication Date
GB343116A true GB343116A (en) 1931-02-16

Family

ID=6243795

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31454/29A Expired GB343116A (en) 1928-10-16 1929-10-16 Manufacture of oily polymerisation products from butadiene or a homologue thereof

Country Status (1)

Country Link
GB (1) GB343116A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2423179A (en) * 1942-09-07 1947-07-01 Union Oil Co Recovery of dienes by polymerization and depolymerization
US2431403A (en) * 1945-12-28 1947-11-25 Sun Oil Co Polymerization of butadiene
US2499505A (en) * 1945-11-20 1950-03-07 Sun Oil Co Vinylcyclohexene hydrochlorides
US2501382A (en) * 1946-03-21 1950-03-21 Phillips Petroleum Co Production of styrene and halogenated styrene
US2504016A (en) * 1947-03-14 1950-04-11 Du Pont Cyclooctadienes and their preparation
US2543092A (en) * 1945-11-16 1951-02-27 Sun Oil Co Dimerization of vinylcyclohexene
US2544808A (en) * 1947-09-25 1951-03-13 Koppers Co Inc Dimerization of butadiene
US2576515A (en) * 1948-03-18 1951-11-27 Sun Oil Co Polymerization of vinylcyclohexene
US2590971A (en) * 1945-11-24 1952-04-01 Sun Oil Co Hydrogenated vinylcyclohexenedimer
US2631173A (en) * 1949-01-04 1953-03-10 Phillips Petroleum Co Production of cyclooctadiene
US3238265A (en) * 1960-09-21 1966-03-01 Basf Ag Production of oligomers of 1, 3-dienes

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2423179A (en) * 1942-09-07 1947-07-01 Union Oil Co Recovery of dienes by polymerization and depolymerization
US2543092A (en) * 1945-11-16 1951-02-27 Sun Oil Co Dimerization of vinylcyclohexene
US2499505A (en) * 1945-11-20 1950-03-07 Sun Oil Co Vinylcyclohexene hydrochlorides
US2590971A (en) * 1945-11-24 1952-04-01 Sun Oil Co Hydrogenated vinylcyclohexenedimer
US2431403A (en) * 1945-12-28 1947-11-25 Sun Oil Co Polymerization of butadiene
US2501382A (en) * 1946-03-21 1950-03-21 Phillips Petroleum Co Production of styrene and halogenated styrene
US2504016A (en) * 1947-03-14 1950-04-11 Du Pont Cyclooctadienes and their preparation
US2544808A (en) * 1947-09-25 1951-03-13 Koppers Co Inc Dimerization of butadiene
US2576515A (en) * 1948-03-18 1951-11-27 Sun Oil Co Polymerization of vinylcyclohexene
US2631173A (en) * 1949-01-04 1953-03-10 Phillips Petroleum Co Production of cyclooctadiene
US3238265A (en) * 1960-09-21 1966-03-01 Basf Ag Production of oligomers of 1, 3-dienes

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