Preparation of Block Copolymers of Vinyl Acetate in. Viscous Poor Solvents
Stable macroradicals of poly(vinyl acetate) were produced by heating vinyl acetate (VAC) and 2% tert-butyl peroxypivalate at 50° C for 96 hr in silicone oil. Block copolymers were produced from these macroradicals by adding a second vinyl monomer and heating at 50° C for an additional 72 hr. The for...
Gespeichert in:
Veröffentlicht in: | Journal of macromolecular science. Chemistry 1977-01, Vol.11 (1), p.53-64 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 64 |
---|---|
container_issue | 1 |
container_start_page | 53 |
container_title | Journal of macromolecular science. Chemistry |
container_volume | 11 |
creator | Seymour, Raymond B. Stahl, G. Allan |
description | Stable macroradicals of poly(vinyl acetate) were produced by heating vinyl acetate (VAC) and 2% tert-butyl peroxypivalate at 50° C for 96 hr in silicone oil. Block copolymers were produced from these macroradicals by adding a second vinyl monomer and heating at 50° C for an additional 72 hr. The formation of these macroradicals was monitored by yield, dilatometric rate data, and scanning electron micrographs. Poly(vinyl acetate-b-methyl methacrylate), polyvinyl acetate-b-acrylic acid), polyvinyl acetate-b-acrylonitrile), poly(vinyl acetate-b-vinylpyrrolidone), poly(vinyl acetate-b-styrene), and polyvinyl acetate-b-methyl methacrylate-b-styrene) were characterized by yield, selective precipitation, pyrolysis gas chromatograph, and differential scanning calorimetry (DSC). |
doi_str_mv | 10.1080/00222337708061251 |
format | Article |
fullrecord | <record><control><sourceid>crossref_infor</sourceid><recordid>TN_cdi_crossref_primary_10_1080_00222337708061251</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1080_00222337708061251</sourcerecordid><originalsourceid>FETCH-LOGICAL-c228t-fd4439edea14dfc283fe21deb76e64e3aa9f4848c4f4082d99ce5bc3ffdd581f3</originalsourceid><addsrcrecordid>eNp1kMtKA0EQRXuhYIj5AHf9AxP7NZMecBODTwQDPnA3dLqrYLQzFbpHZf7eCXEn3k1xD5xaXMbOpJhLYcW5EEoprReLsVRSlfKITfasGOHbCZvl_C7GlKWwlZqw-3WCnUuub6njhPwykv_gK9pRHLaQ8p69tt0Q-dJD73rgbTcfSfb0mfmaKPEnil_Q9fmUHaOLGWa_d8perq-eV7fFw-PN3Wr5UHilbF9gMEbXEMBJE9ArqxGUDLBZVFAZ0M7VaKyx3qARVoW69lBuvEYMobQS9ZTJw1-fKOcE2OxSu3VpaKRo9hs0fzYYnYuD03ZIaeu-KcXQ9G6IlDC5zre50f_rPz-kZFQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Preparation of Block Copolymers of Vinyl Acetate in. Viscous Poor Solvents</title><source>Taylor & Francis</source><creator>Seymour, Raymond B. ; Stahl, G. Allan</creator><creatorcontrib>Seymour, Raymond B. ; Stahl, G. Allan</creatorcontrib><description>Stable macroradicals of poly(vinyl acetate) were produced by heating vinyl acetate (VAC) and 2% tert-butyl peroxypivalate at 50° C for 96 hr in silicone oil. Block copolymers were produced from these macroradicals by adding a second vinyl monomer and heating at 50° C for an additional 72 hr. The formation of these macroradicals was monitored by yield, dilatometric rate data, and scanning electron micrographs. Poly(vinyl acetate-b-methyl methacrylate), polyvinyl acetate-b-acrylic acid), polyvinyl acetate-b-acrylonitrile), poly(vinyl acetate-b-vinylpyrrolidone), poly(vinyl acetate-b-styrene), and polyvinyl acetate-b-methyl methacrylate-b-styrene) were characterized by yield, selective precipitation, pyrolysis gas chromatograph, and differential scanning calorimetry (DSC).</description><identifier>ISSN: 0022-233X</identifier><identifier>DOI: 10.1080/00222337708061251</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><ispartof>Journal of macromolecular science. Chemistry, 1977-01, Vol.11 (1), p.53-64</ispartof><rights>Copyright Taylor & Francis Group, LLC 1977</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c228t-fd4439edea14dfc283fe21deb76e64e3aa9f4848c4f4082d99ce5bc3ffdd581f3</citedby><cites>FETCH-LOGICAL-c228t-fd4439edea14dfc283fe21deb76e64e3aa9f4848c4f4082d99ce5bc3ffdd581f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/00222337708061251$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/00222337708061251$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,59624,60413</link.rule.ids></links><search><creatorcontrib>Seymour, Raymond B.</creatorcontrib><creatorcontrib>Stahl, G. Allan</creatorcontrib><title>Preparation of Block Copolymers of Vinyl Acetate in. Viscous Poor Solvents</title><title>Journal of macromolecular science. Chemistry</title><description>Stable macroradicals of poly(vinyl acetate) were produced by heating vinyl acetate (VAC) and 2% tert-butyl peroxypivalate at 50° C for 96 hr in silicone oil. Block copolymers were produced from these macroradicals by adding a second vinyl monomer and heating at 50° C for an additional 72 hr. The formation of these macroradicals was monitored by yield, dilatometric rate data, and scanning electron micrographs. Poly(vinyl acetate-b-methyl methacrylate), polyvinyl acetate-b-acrylic acid), polyvinyl acetate-b-acrylonitrile), poly(vinyl acetate-b-vinylpyrrolidone), poly(vinyl acetate-b-styrene), and polyvinyl acetate-b-methyl methacrylate-b-styrene) were characterized by yield, selective precipitation, pyrolysis gas chromatograph, and differential scanning calorimetry (DSC).</description><issn>0022-233X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1977</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKA0EQRXuhYIj5AHf9AxP7NZMecBODTwQDPnA3dLqrYLQzFbpHZf7eCXEn3k1xD5xaXMbOpJhLYcW5EEoprReLsVRSlfKITfasGOHbCZvl_C7GlKWwlZqw-3WCnUuub6njhPwykv_gK9pRHLaQ8p69tt0Q-dJD73rgbTcfSfb0mfmaKPEnil_Q9fmUHaOLGWa_d8perq-eV7fFw-PN3Wr5UHilbF9gMEbXEMBJE9ArqxGUDLBZVFAZ0M7VaKyx3qARVoW69lBuvEYMobQS9ZTJw1-fKOcE2OxSu3VpaKRo9hs0fzYYnYuD03ZIaeu-KcXQ9G6IlDC5zre50f_rPz-kZFQ</recordid><startdate>19770101</startdate><enddate>19770101</enddate><creator>Seymour, Raymond B.</creator><creator>Stahl, G. Allan</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19770101</creationdate><title>Preparation of Block Copolymers of Vinyl Acetate in. Viscous Poor Solvents</title><author>Seymour, Raymond B. ; Stahl, G. Allan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c228t-fd4439edea14dfc283fe21deb76e64e3aa9f4848c4f4082d99ce5bc3ffdd581f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1977</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Seymour, Raymond B.</creatorcontrib><creatorcontrib>Stahl, G. Allan</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of macromolecular science. Chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seymour, Raymond B.</au><au>Stahl, G. Allan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of Block Copolymers of Vinyl Acetate in. Viscous Poor Solvents</atitle><jtitle>Journal of macromolecular science. Chemistry</jtitle><date>1977-01-01</date><risdate>1977</risdate><volume>11</volume><issue>1</issue><spage>53</spage><epage>64</epage><pages>53-64</pages><issn>0022-233X</issn><abstract>Stable macroradicals of poly(vinyl acetate) were produced by heating vinyl acetate (VAC) and 2% tert-butyl peroxypivalate at 50° C for 96 hr in silicone oil. Block copolymers were produced from these macroradicals by adding a second vinyl monomer and heating at 50° C for an additional 72 hr. The formation of these macroradicals was monitored by yield, dilatometric rate data, and scanning electron micrographs. Poly(vinyl acetate-b-methyl methacrylate), polyvinyl acetate-b-acrylic acid), polyvinyl acetate-b-acrylonitrile), poly(vinyl acetate-b-vinylpyrrolidone), poly(vinyl acetate-b-styrene), and polyvinyl acetate-b-methyl methacrylate-b-styrene) were characterized by yield, selective precipitation, pyrolysis gas chromatograph, and differential scanning calorimetry (DSC).</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/00222337708061251</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-233X |
ispartof | Journal of macromolecular science. Chemistry, 1977-01, Vol.11 (1), p.53-64 |
issn | 0022-233X |
language | eng |
recordid | cdi_crossref_primary_10_1080_00222337708061251 |
source | Taylor & Francis |
title | Preparation of Block Copolymers of Vinyl Acetate in. Viscous Poor Solvents |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T04%3A00%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Preparation%20of%20Block%20Copolymers%20of%20Vinyl%20Acetate%20in.%20Viscous%20Poor%20Solvents&rft.jtitle=Journal%20of%20macromolecular%20science.%20Chemistry&rft.au=Seymour,%20Raymond%20B.&rft.date=1977-01-01&rft.volume=11&rft.issue=1&rft.spage=53&rft.epage=64&rft.pages=53-64&rft.issn=0022-233X&rft_id=info:doi/10.1080/00222337708061251&rft_dat=%3Ccrossref_infor%3E10_1080_00222337708061251%3C/crossref_infor%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 |