Production of a new type of butadiene polymer
1,138,299. Stereoblock butadiene polymers. BADISCHE ANILIN- & SODA-FABRIK A.G. 3 May, 1966 [4 May, 1965], No. 19366/66. Heading C3P. Stereoblock polymers are made by polymerizing butadiene with a Ziegler-Natta type catalyst comprising an alkyl metal compound and a compound of a transition metal...
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description | 1,138,299. Stereoblock butadiene polymers. BADISCHE ANILIN- & SODA-FABRIK A.G. 3 May, 1966 [4 May, 1965], No. 19366/66. Heading C3P. Stereoblock polymers are made by polymerizing butadiene with a Ziegler-Natta type catalyst comprising an alkyl metal compound and a compound of a transition metal of Groups IV to VIII, and whilst unreacted butadiene is still present in the polymerization mixture adding a catalyst of the same type but which converts butadiene into a polymer whose configuration is different to the configuration of the polybutadiene first prepared, and continuing the polymerization. In examples, effected in solvents, the following catalysts are used: (1) (C 2 H 5 ) 3 Al, AlBr 3 , and TiI 4 , followed by (C 2 H 5 ) 3 Al and VCl 3 , (2) as (1) but VCl 3 replaced by VCl 4 , (3) (C 4 H 9 ) 3 Al and TiCl 3 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (4) (C 4 H 9 ) 2 AlCl and TiCl 3 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (5) (C 2 H 5 ) 3 Al and TiCl 4 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (6) (C 4 H 9 ) 3 Al and Ti(-OC 4 H 9 ) 4 , followed by (C 2 H 5 ) 3 Al and VCl 3 , (7) Cr triacetylacetonate and (C 4 H 9 ) 3 Al followed by (C 4 H 9 ) 3 Al, (8) Sn(C 4 H 9 ) 4 and ZrCl 4 , followed by amyl Na and TiCl 3 . The polymers may be sulphur vulcanized. |
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Stereoblock polymers are made by polymerizing butadiene with a Ziegler-Natta type catalyst comprising an alkyl metal compound and a compound of a transition metal of Groups IV to VIII, and whilst unreacted butadiene is still present in the polymerization mixture adding a catalyst of the same type but which converts butadiene into a polymer whose configuration is different to the configuration of the polybutadiene first prepared, and continuing the polymerization. In examples, effected in solvents, the following catalysts are used: (1) (C 2 H 5 ) 3 Al, AlBr 3 , and TiI 4 , followed by (C 2 H 5 ) 3 Al and VCl 3 , (2) as (1) but VCl 3 replaced by VCl 4 , (3) (C 4 H 9 ) 3 Al and TiCl 3 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (4) (C 4 H 9 ) 2 AlCl and TiCl 3 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (5) (C 2 H 5 ) 3 Al and TiCl 4 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (6) (C 4 H 9 ) 3 Al and Ti(-OC 4 H 9 ) 4 , followed by (C 2 H 5 ) 3 Al and VCl 3 , (7) Cr triacetylacetonate and (C 4 H 9 ) 3 Al followed by (C 4 H 9 ) 3 Al, (8) Sn(C 4 H 9 ) 4 and ZrCl 4 , followed by amyl Na and TiCl 3 . The polymers may be sulphur vulcanized.</description><language>eng</language><subject>CHEMISTRY ; COMPOSITIONS BASED THEREON ; MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS ; METALLURGY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><creationdate>1968</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19681227&DB=EPODOC&CC=GB&NR=1138299A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19681227&DB=EPODOC&CC=GB&NR=1138299A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NAARMANN HERBERT</creatorcontrib><creatorcontrib>KASTNING ERNST-GUENTHER</creatorcontrib><title>Production of a new type of butadiene polymer</title><description>1,138,299. Stereoblock butadiene polymers. BADISCHE ANILIN- & SODA-FABRIK A.G. 3 May, 1966 [4 May, 1965], No. 19366/66. Heading C3P. Stereoblock polymers are made by polymerizing butadiene with a Ziegler-Natta type catalyst comprising an alkyl metal compound and a compound of a transition metal of Groups IV to VIII, and whilst unreacted butadiene is still present in the polymerization mixture adding a catalyst of the same type but which converts butadiene into a polymer whose configuration is different to the configuration of the polybutadiene first prepared, and continuing the polymerization. In examples, effected in solvents, the following catalysts are used: (1) (C 2 H 5 ) 3 Al, AlBr 3 , and TiI 4 , followed by (C 2 H 5 ) 3 Al and VCl 3 , (2) as (1) but VCl 3 replaced by VCl 4 , (3) (C 4 H 9 ) 3 Al and TiCl 3 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (4) (C 4 H 9 ) 2 AlCl and TiCl 3 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (5) (C 2 H 5 ) 3 Al and TiCl 4 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (6) (C 4 H 9 ) 3 Al and Ti(-OC 4 H 9 ) 4 , followed by (C 2 H 5 ) 3 Al and VCl 3 , (7) Cr triacetylacetonate and (C 4 H 9 ) 3 Al followed by (C 4 H 9 ) 3 Al, (8) Sn(C 4 H 9 ) 4 and ZrCl 4 , followed by amyl Na and TiCl 3 . The polymers may be sulphur vulcanized.</description><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</subject><subject>METALLURGY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1968</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNANKMpPKU0uyczPU8hPU0hUyEstVyipLEgF8ZJKSxJTMlPzUhUK8nMqc1OLeBhY0xJzilN5oTQ3g7yba4izh25qQX58anFBYjJQcUm8u5OhobGFkaWlozFhFQAHjykZ</recordid><startdate>19681227</startdate><enddate>19681227</enddate><creator>NAARMANN HERBERT</creator><creator>KASTNING ERNST-GUENTHER</creator><scope>EVB</scope></search><sort><creationdate>19681227</creationdate><title>Production of a new type of butadiene polymer</title><author>NAARMANN HERBERT ; KASTNING ERNST-GUENTHER</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_GB1138299A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1968</creationdate><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</topic><topic>METALLURGY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><toplevel>online_resources</toplevel><creatorcontrib>NAARMANN HERBERT</creatorcontrib><creatorcontrib>KASTNING ERNST-GUENTHER</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NAARMANN HERBERT</au><au>KASTNING ERNST-GUENTHER</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Production of a new type of butadiene polymer</title><date>1968-12-27</date><risdate>1968</risdate><abstract>1,138,299. Stereoblock butadiene polymers. BADISCHE ANILIN- & SODA-FABRIK A.G. 3 May, 1966 [4 May, 1965], No. 19366/66. Heading C3P. Stereoblock polymers are made by polymerizing butadiene with a Ziegler-Natta type catalyst comprising an alkyl metal compound and a compound of a transition metal of Groups IV to VIII, and whilst unreacted butadiene is still present in the polymerization mixture adding a catalyst of the same type but which converts butadiene into a polymer whose configuration is different to the configuration of the polybutadiene first prepared, and continuing the polymerization. In examples, effected in solvents, the following catalysts are used: (1) (C 2 H 5 ) 3 Al, AlBr 3 , and TiI 4 , followed by (C 2 H 5 ) 3 Al and VCl 3 , (2) as (1) but VCl 3 replaced by VCl 4 , (3) (C 4 H 9 ) 3 Al and TiCl 3 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (4) (C 4 H 9 ) 2 AlCl and TiCl 3 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (5) (C 2 H 5 ) 3 Al and TiCl 4 , followed by (C 2 H 5 ) 2 AlI and TiCl 3 , (6) (C 4 H 9 ) 3 Al and Ti(-OC 4 H 9 ) 4 , followed by (C 2 H 5 ) 3 Al and VCl 3 , (7) Cr triacetylacetonate and (C 4 H 9 ) 3 Al followed by (C 4 H 9 ) 3 Al, (8) Sn(C 4 H 9 ) 4 and ZrCl 4 , followed by amyl Na and TiCl 3 . The polymers may be sulphur vulcanized.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY COMPOSITIONS BASED THEREON MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS METALLURGY ORGANIC MACROMOLECULAR COMPOUNDS THEIR PREPARATION OR CHEMICAL WORKING-UP |
title | Production of a new type of butadiene polymer |
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