LIQUID POLYISOPRENE AND ITS PRODUCTION

PURPOSE:To obtain easily a liquid polyisoprene, which is superior in reactivity, a compatibility and storage stability and with which a material superior in water resistance, low-temperature property, etc., is produced for specified purposes, by reacting a liquid isoprene polymer with a compound hav...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: TSURUSHITA KENJI, MISUMI AKIHIRO, OKAMOTO KOHEI, FUJII ISAO
Format: Patent
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator TSURUSHITA KENJI
MISUMI AKIHIRO
OKAMOTO KOHEI
FUJII ISAO
description PURPOSE:To obtain easily a liquid polyisoprene, which is superior in reactivity, a compatibility and storage stability and with which a material superior in water resistance, low-temperature property, etc., is produced for specified purposes, by reacting a liquid isoprene polymer with a compound having an epoxy radical. CONSTITUTION:An isoprene polymer, which has, e.g., 50mol% or more 1,4-bondings and 50mol% or less 1,2- and/or 3,4-bondings, is reacted with H2O2 to form a liquid isoprene polymer (A). This polymer (A) mainly consists of structural units derived from the original isoprene polymer and has 1 or more OH-radicals per molecule at the ends of its molecular chain. Its number-average MW is 300-25000 and its OH- radical content is 0.1-10milli-equivalent. Next, component A is mixed with a compound (B) which has an epoxy-radical, such as glycidyl isocyanate compound, in a proportion of 0.6mol or more of component B per equivalent of the OH-radical in component A, and allowed to react with each other in the presence or absence of a solvent at 0-200 deg.C under ordinary pressure- 100kg/cm G for 0.1-100hr. the title liquid polyisoprene which has 1 or more epoxy-radicals per molecule at the ends of its molecular chains and whose number-average MW is 400-26000 and epoxy equivalent is 100-13000 is thus obtained.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_JPS6414207A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JPS6414207A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_JPS6414207A3</originalsourceid><addsrcrecordid>eNrjZFDz8QwM9XRRCPD3ifQM9g8IcvVzVXD0c1HwDAlWCAjydwl1DvH09-NhYE1LzClO5YXS3AwKbq4hzh66qQX58anFBYnJqXmpJfFeAcFmJoYmRgbmjsZEKAEAoTkjrg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>LIQUID POLYISOPRENE AND ITS PRODUCTION</title><source>esp@cenet</source><creator>TSURUSHITA KENJI ; MISUMI AKIHIRO ; OKAMOTO KOHEI ; FUJII ISAO</creator><creatorcontrib>TSURUSHITA KENJI ; MISUMI AKIHIRO ; OKAMOTO KOHEI ; FUJII ISAO</creatorcontrib><description>PURPOSE:To obtain easily a liquid polyisoprene, which is superior in reactivity, a compatibility and storage stability and with which a material superior in water resistance, low-temperature property, etc., is produced for specified purposes, by reacting a liquid isoprene polymer with a compound having an epoxy radical. CONSTITUTION:An isoprene polymer, which has, e.g., 50mol% or more 1,4-bondings and 50mol% or less 1,2- and/or 3,4-bondings, is reacted with H2O2 to form a liquid isoprene polymer (A). This polymer (A) mainly consists of structural units derived from the original isoprene polymer and has 1 or more OH-radicals per molecule at the ends of its molecular chain. Its number-average MW is 300-25000 and its OH- radical content is 0.1-10milli-equivalent. Next, component A is mixed with a compound (B) which has an epoxy-radical, such as glycidyl isocyanate compound, in a proportion of 0.6mol or more of component B per equivalent of the OH-radical in component A, and allowed to react with each other in the presence or absence of a solvent at 0-200 deg.C under ordinary pressure- 100kg/cm G for 0.1-100hr. the title liquid polyisoprene which has 1 or more epoxy-radicals per molecule at the ends of its molecular chains and whose number-average MW is 400-26000 and epoxy equivalent is 100-13000 is thus obtained.</description><language>eng</language><subject>CHEMISTRY ; COMPOSITIONS BASED THEREON ; MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS ; MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS ; METALLURGY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><creationdate>1989</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&amp;date=19890118&amp;DB=EPODOC&amp;CC=JP&amp;NR=S6414207A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19890118&amp;DB=EPODOC&amp;CC=JP&amp;NR=S6414207A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>TSURUSHITA KENJI</creatorcontrib><creatorcontrib>MISUMI AKIHIRO</creatorcontrib><creatorcontrib>OKAMOTO KOHEI</creatorcontrib><creatorcontrib>FUJII ISAO</creatorcontrib><title>LIQUID POLYISOPRENE AND ITS PRODUCTION</title><description>PURPOSE:To obtain easily a liquid polyisoprene, which is superior in reactivity, a compatibility and storage stability and with which a material superior in water resistance, low-temperature property, etc., is produced for specified purposes, by reacting a liquid isoprene polymer with a compound having an epoxy radical. CONSTITUTION:An isoprene polymer, which has, e.g., 50mol% or more 1,4-bondings and 50mol% or less 1,2- and/or 3,4-bondings, is reacted with H2O2 to form a liquid isoprene polymer (A). This polymer (A) mainly consists of structural units derived from the original isoprene polymer and has 1 or more OH-radicals per molecule at the ends of its molecular chain. Its number-average MW is 300-25000 and its OH- radical content is 0.1-10milli-equivalent. Next, component A is mixed with a compound (B) which has an epoxy-radical, such as glycidyl isocyanate compound, in a proportion of 0.6mol or more of component B per equivalent of the OH-radical in component A, and allowed to react with each other in the presence or absence of a solvent at 0-200 deg.C under ordinary pressure- 100kg/cm G for 0.1-100hr. the title liquid polyisoprene which has 1 or more epoxy-radicals per molecule at the ends of its molecular chains and whose number-average MW is 400-26000 and epoxy equivalent is 100-13000 is thus obtained.</description><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON 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>1989</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFDz8QwM9XRRCPD3ifQM9g8IcvVzVXD0c1HwDAlWCAjydwl1DvH09-NhYE1LzClO5YXS3AwKbq4hzh66qQX58anFBYnJqXmpJfFeAcFmJoYmRgbmjsZEKAEAoTkjrg</recordid><startdate>19890118</startdate><enddate>19890118</enddate><creator>TSURUSHITA KENJI</creator><creator>MISUMI AKIHIRO</creator><creator>OKAMOTO KOHEI</creator><creator>FUJII ISAO</creator><scope>EVB</scope></search><sort><creationdate>19890118</creationdate><title>LIQUID POLYISOPRENE AND ITS PRODUCTION</title><author>TSURUSHITA KENJI ; MISUMI AKIHIRO ; OKAMOTO KOHEI ; FUJII ISAO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPS6414207A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1989</creationdate><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</topic><topic>METALLURGY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><toplevel>online_resources</toplevel><creatorcontrib>TSURUSHITA KENJI</creatorcontrib><creatorcontrib>MISUMI AKIHIRO</creatorcontrib><creatorcontrib>OKAMOTO KOHEI</creatorcontrib><creatorcontrib>FUJII ISAO</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>TSURUSHITA KENJI</au><au>MISUMI AKIHIRO</au><au>OKAMOTO KOHEI</au><au>FUJII ISAO</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>LIQUID POLYISOPRENE AND ITS PRODUCTION</title><date>1989-01-18</date><risdate>1989</risdate><abstract>PURPOSE:To obtain easily a liquid polyisoprene, which is superior in reactivity, a compatibility and storage stability and with which a material superior in water resistance, low-temperature property, etc., is produced for specified purposes, by reacting a liquid isoprene polymer with a compound having an epoxy radical. CONSTITUTION:An isoprene polymer, which has, e.g., 50mol% or more 1,4-bondings and 50mol% or less 1,2- and/or 3,4-bondings, is reacted with H2O2 to form a liquid isoprene polymer (A). This polymer (A) mainly consists of structural units derived from the original isoprene polymer and has 1 or more OH-radicals per molecule at the ends of its molecular chain. Its number-average MW is 300-25000 and its OH- radical content is 0.1-10milli-equivalent. Next, component A is mixed with a compound (B) which has an epoxy-radical, such as glycidyl isocyanate compound, in a proportion of 0.6mol or more of component B per equivalent of the OH-radical in component A, and allowed to react with each other in the presence or absence of a solvent at 0-200 deg.C under ordinary pressure- 100kg/cm G for 0.1-100hr. the title liquid polyisoprene which has 1 or more epoxy-radicals per molecule at the ends of its molecular chains and whose number-average MW is 400-26000 and epoxy equivalent is 100-13000 is thus obtained.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_JPS6414207A
source esp@cenet
subjects CHEMISTRY
COMPOSITIONS BASED THEREON
MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS
MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
METALLURGY
ORGANIC MACROMOLECULAR COMPOUNDS
THEIR PREPARATION OR CHEMICAL WORKING-UP
title LIQUID POLYISOPRENE AND ITS PRODUCTION
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T17%3A56%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=TSURUSHITA%20KENJI&rft.date=1989-01-18&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EJPS6414207A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true