GB606112A - Process for recovering cyclopentadiene - Google Patents

Process for recovering cyclopentadiene

Info

Publication number
GB606112A
GB606112A GB25031/44A GB2503144A GB606112A GB 606112 A GB606112 A GB 606112A GB 25031/44 A GB25031/44 A GB 25031/44A GB 2503144 A GB2503144 A GB 2503144A GB 606112 A GB606112 A GB 606112A
Authority
GB
United Kingdom
Prior art keywords
cyclopentadiene
forerunnings
stored
dimer
distillation
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
GB25031/44A
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.)
Carnegie Illinois Steel Corp
Original Assignee
Carnegie Illinois Steel Corp
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 Carnegie Illinois Steel Corp filed Critical Carnegie Illinois Steel Corp
Publication of GB606112A publication Critical patent/GB606112A/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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Benzol forerunnings containing cyclopentadiene are stored at atmospheric temperatures and pressures out of contact with oxygen or oxygen-containing gas to polymerize cyclopentadiene to the dimer with at most minor amounts of higher polymers, other constituents originally present are removed by distillation at not more than 120 DEG C. to avoid depolymerization and the dicyclopentadiene purified. The forerunnings, which must be substantially free of benzene and its homologues, are stored in closed containers at not substantially below 15 DEG C. or above 40 DEG C. A halide catalyst such as stannic chloride or boron fluoride may be added. The storage time varies from a few days to a few weeks. After the distillation, the residue is fractionated under vacuum to recover the dimer. In an example, forerunnings of B.R. 31-46 DEG C. are stored at 22-25.5 DEG C. for 34 days and solid dicyclopentadiene recovered. This may be transported in an inert atmosphere such as natural gas or nitrogen, and depolymerized as required to cyclopentadiene for use in the production of synthetic rubber or, with maleic anhydride, resins.ALSO:Benzol forerunnings containing cyclopentadiene are stored at atmospheric temperatures and pressures out of contact with oxygen or oxygen-containing gas to polymerize cyclopentadiene to the dimer with at most minor amounts of higher polymers, other constituents originally present are removed by distillation at not more than 120 DEG C. to avoid depolymerization and the dicyclopentadiene purified. The forerunnings, which must be substantially free of benzene and its homologues, are stored in closed containers at not substantially below 15 DEG C. or above 40 DEG C. A halide catalyst such as stannic chloride or boron fluoride may be added. The storage time varies from a few days to a few weeks. After the distillation, the residue is fractionated under vacuum to recover the dimer. In an example, forerunnings of B.R. 31-46 DEG C. are stored at 22-25.5 DEG C. for 34 days, and solid dicyclopentadiene recovered. This may be transported in an inert atmosphere such as natural gas or nitrogen, and depolymerized as required to cyclopentadiene for use in the production of synthetic rubber or, with maleic anhydride, resins.
GB25031/44A 1941-07-17 1945-01-05 Process for recovering cyclopentadiene Expired GB606112A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US606112XA 1941-07-17 1941-07-17

Publications (1)

Publication Number Publication Date
GB606112A true GB606112A (en) 1948-08-06

Family

ID=22030611

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25031/44A Expired GB606112A (en) 1941-07-17 1945-01-05 Process for recovering cyclopentadiene

Country Status (2)

Country Link
BE (1) BE606112A (en)
GB (1) GB606112A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1060389B (en) * 1956-02-28 1959-07-02 Bataafsche Petroleum Process for obtaining dicyclopentadiene of high purity

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1060389B (en) * 1956-02-28 1959-07-02 Bataafsche Petroleum Process for obtaining dicyclopentadiene of high purity

Also Published As

Publication number Publication date
BE606112A (en) 1961-11-03

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