Loading…
N-(Substituted phenyl) itaconimides as organic stabilizers for plasticized poly(vinyl chloride) against photo-degradation
Several N-(substituted phenyl)itaconimide derivatives, N-(RPh)II (R: –NO 2, –COOH, –H, –OH, –OMe, –Me, –Cl, or –Br), have been investigated as organic photo-stabilizers for poly(vinyl chloride) (PVC) plasticized with dioctyl phthalate (DOP). Their stabilizing efficiencies are evaluated by measuring...
Saved in:
Published in: | Polymer degradation and stability 2007-04, Vol.92 (4), p.733-740 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c394t-dc5bc2a7cfc1cd72e337be297c11b63436de82ff71aef70fd74aa842562e68f03 |
---|---|
cites | cdi_FETCH-LOGICAL-c394t-dc5bc2a7cfc1cd72e337be297c11b63436de82ff71aef70fd74aa842562e68f03 |
container_end_page | 740 |
container_issue | 4 |
container_start_page | 733 |
container_title | Polymer degradation and stability |
container_volume | 92 |
creator | Fahmi, Mona Mohamed Mohamed, Nadia Ahmed |
description | Several
N-(substituted phenyl)itaconimide derivatives,
N-(RPh)II (R: –NO
2, –COOH, –H, –OH, –OMe, –Me, –Cl, or –Br), have been investigated as organic photo-stabilizers for poly(vinyl chloride) (PVC) plasticized with dioctyl phthalate (DOP). Their stabilizing efficiencies are evaluated by measuring the length of the induction period (Ts), the period during which no detectable amounts of hydrogen chloride gas could be observed, and also from the rate of dehydrochlorination as measured by continuous potentiometric determination, and the extent of discolouration of the degraded polymer. The efficiencies are also evaluated by determining the amount of gel formation as well as the intrinsic viscosity of the insoluble and the soluble fractions of the degraded polymer, respectively. The results have proved the greater stabilizing efficiency of the
N-(RPh)II derivatives relative to that of the phenyl salicylate UV absorber which is a commonly used industrial stabilizer. A radical mechanism is proposed to account for the stabilizing action of the investigated products. |
doi_str_mv | 10.1016/j.polymdegradstab.2006.11.019 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_29889395</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0141391007000328</els_id><sourcerecordid>29889395</sourcerecordid><originalsourceid>FETCH-LOGICAL-c394t-dc5bc2a7cfc1cd72e337be297c11b63436de82ff71aef70fd74aa842562e68f03</originalsourceid><addsrcrecordid>eNqNkEFr3DAQhUVoIdu0_8GXlORgVyN5LfvQQwltGgjtIelZjKXRRovXciVtYPvrq2UDhZ4yF8HwvvdGj7FL4A1w6D5tmyVMh52lTUSbMo6N4LxrABoOwxlbQa9kLaSAN2zFoYVaDsDP2buUtrxMu4YVO_yorx72Y8o-7zPZanmi-TBdVz6jCbPfeUupwlSFuMHZm-oY4yf_h2KqXIjVMmFhTVkUtlxz9ewLX5mnKcTCXle4QT-nXIxDDvXpVsw-zO_ZW4dTog8v7wX79e3r4833-v7n7d3Nl_vayKHNtTXr0QhUxhkwVgmSUo0kBmUAxk62srPUC-cUIDnFnVUtYt-KdSeo6x2XF-zjyXeJ4feeUtY7nwxNE84U9kmLoe8HOayL8PNJaGJIKZLTS_Q7jAcNXB8L11v9X-H6WLgG0KXwwl--BGEyOLmIs_Hpn0nf9UopWXS3Jx2VXz97ijoZT7Mh6yOZrG3wr0z8C4E3pEY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>29889395</pqid></control><display><type>article</type><title>N-(Substituted phenyl) itaconimides as organic stabilizers for plasticized poly(vinyl chloride) against photo-degradation</title><source>ScienceDirect Journals</source><creator>Fahmi, Mona Mohamed ; Mohamed, Nadia Ahmed</creator><creatorcontrib>Fahmi, Mona Mohamed ; Mohamed, Nadia Ahmed</creatorcontrib><description>Several
N-(substituted phenyl)itaconimide derivatives,
N-(RPh)II (R: –NO
2, –COOH, –H, –OH, –OMe, –Me, –Cl, or –Br), have been investigated as organic photo-stabilizers for poly(vinyl chloride) (PVC) plasticized with dioctyl phthalate (DOP). Their stabilizing efficiencies are evaluated by measuring the length of the induction period (Ts), the period during which no detectable amounts of hydrogen chloride gas could be observed, and also from the rate of dehydrochlorination as measured by continuous potentiometric determination, and the extent of discolouration of the degraded polymer. The efficiencies are also evaluated by determining the amount of gel formation as well as the intrinsic viscosity of the insoluble and the soluble fractions of the degraded polymer, respectively. The results have proved the greater stabilizing efficiency of the
N-(RPh)II derivatives relative to that of the phenyl salicylate UV absorber which is a commonly used industrial stabilizer. A radical mechanism is proposed to account for the stabilizing action of the investigated products.</description><identifier>ISSN: 0141-3910</identifier><identifier>EISSN: 1873-2321</identifier><identifier>DOI: 10.1016/j.polymdegradstab.2006.11.019</identifier><identifier>CODEN: PDSTDW</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Compounding ingredients ; Cross-linking ; Discolouration ; Exact sciences and technology ; Organic photo-stabilizers ; Photo-dehydrochlorination ; Plasticized poly(vinyl chloride) ; Polymer industry, paints, wood ; Stabilization mechanism ; Stabilizers (antioxydants, antiozonants, etc.) ; Technology of polymers</subject><ispartof>Polymer degradation and stability, 2007-04, Vol.92 (4), p.733-740</ispartof><rights>2007 Elsevier Ltd</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-dc5bc2a7cfc1cd72e337be297c11b63436de82ff71aef70fd74aa842562e68f03</citedby><cites>FETCH-LOGICAL-c394t-dc5bc2a7cfc1cd72e337be297c11b63436de82ff71aef70fd74aa842562e68f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18687773$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Fahmi, Mona Mohamed</creatorcontrib><creatorcontrib>Mohamed, Nadia Ahmed</creatorcontrib><title>N-(Substituted phenyl) itaconimides as organic stabilizers for plasticized poly(vinyl chloride) against photo-degradation</title><title>Polymer degradation and stability</title><description>Several
N-(substituted phenyl)itaconimide derivatives,
N-(RPh)II (R: –NO
2, –COOH, –H, –OH, –OMe, –Me, –Cl, or –Br), have been investigated as organic photo-stabilizers for poly(vinyl chloride) (PVC) plasticized with dioctyl phthalate (DOP). Their stabilizing efficiencies are evaluated by measuring the length of the induction period (Ts), the period during which no detectable amounts of hydrogen chloride gas could be observed, and also from the rate of dehydrochlorination as measured by continuous potentiometric determination, and the extent of discolouration of the degraded polymer. The efficiencies are also evaluated by determining the amount of gel formation as well as the intrinsic viscosity of the insoluble and the soluble fractions of the degraded polymer, respectively. The results have proved the greater stabilizing efficiency of the
N-(RPh)II derivatives relative to that of the phenyl salicylate UV absorber which is a commonly used industrial stabilizer. A radical mechanism is proposed to account for the stabilizing action of the investigated products.</description><subject>Applied sciences</subject><subject>Compounding ingredients</subject><subject>Cross-linking</subject><subject>Discolouration</subject><subject>Exact sciences and technology</subject><subject>Organic photo-stabilizers</subject><subject>Photo-dehydrochlorination</subject><subject>Plasticized poly(vinyl chloride)</subject><subject>Polymer industry, paints, wood</subject><subject>Stabilization mechanism</subject><subject>Stabilizers (antioxydants, antiozonants, etc.)</subject><subject>Technology of polymers</subject><issn>0141-3910</issn><issn>1873-2321</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqNkEFr3DAQhUVoIdu0_8GXlORgVyN5LfvQQwltGgjtIelZjKXRRovXciVtYPvrq2UDhZ4yF8HwvvdGj7FL4A1w6D5tmyVMh52lTUSbMo6N4LxrABoOwxlbQa9kLaSAN2zFoYVaDsDP2buUtrxMu4YVO_yorx72Y8o-7zPZanmi-TBdVz6jCbPfeUupwlSFuMHZm-oY4yf_h2KqXIjVMmFhTVkUtlxz9ewLX5mnKcTCXle4QT-nXIxDDvXpVsw-zO_ZW4dTog8v7wX79e3r4833-v7n7d3Nl_vayKHNtTXr0QhUxhkwVgmSUo0kBmUAxk62srPUC-cUIDnFnVUtYt-KdSeo6x2XF-zjyXeJ4feeUtY7nwxNE84U9kmLoe8HOayL8PNJaGJIKZLTS_Q7jAcNXB8L11v9X-H6WLgG0KXwwl--BGEyOLmIs_Hpn0nf9UopWXS3Jx2VXz97ijoZT7Mh6yOZrG3wr0z8C4E3pEY</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Fahmi, Mona Mohamed</creator><creator>Mohamed, Nadia Ahmed</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20070401</creationdate><title>N-(Substituted phenyl) itaconimides as organic stabilizers for plasticized poly(vinyl chloride) against photo-degradation</title><author>Fahmi, Mona Mohamed ; Mohamed, Nadia Ahmed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-dc5bc2a7cfc1cd72e337be297c11b63436de82ff71aef70fd74aa842562e68f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Applied sciences</topic><topic>Compounding ingredients</topic><topic>Cross-linking</topic><topic>Discolouration</topic><topic>Exact sciences and technology</topic><topic>Organic photo-stabilizers</topic><topic>Photo-dehydrochlorination</topic><topic>Plasticized poly(vinyl chloride)</topic><topic>Polymer industry, paints, wood</topic><topic>Stabilization mechanism</topic><topic>Stabilizers (antioxydants, antiozonants, etc.)</topic><topic>Technology of polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fahmi, Mona Mohamed</creatorcontrib><creatorcontrib>Mohamed, Nadia Ahmed</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymer degradation and stability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fahmi, Mona Mohamed</au><au>Mohamed, Nadia Ahmed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N-(Substituted phenyl) itaconimides as organic stabilizers for plasticized poly(vinyl chloride) against photo-degradation</atitle><jtitle>Polymer degradation and stability</jtitle><date>2007-04-01</date><risdate>2007</risdate><volume>92</volume><issue>4</issue><spage>733</spage><epage>740</epage><pages>733-740</pages><issn>0141-3910</issn><eissn>1873-2321</eissn><coden>PDSTDW</coden><abstract>Several
N-(substituted phenyl)itaconimide derivatives,
N-(RPh)II (R: –NO
2, –COOH, –H, –OH, –OMe, –Me, –Cl, or –Br), have been investigated as organic photo-stabilizers for poly(vinyl chloride) (PVC) plasticized with dioctyl phthalate (DOP). Their stabilizing efficiencies are evaluated by measuring the length of the induction period (Ts), the period during which no detectable amounts of hydrogen chloride gas could be observed, and also from the rate of dehydrochlorination as measured by continuous potentiometric determination, and the extent of discolouration of the degraded polymer. The efficiencies are also evaluated by determining the amount of gel formation as well as the intrinsic viscosity of the insoluble and the soluble fractions of the degraded polymer, respectively. The results have proved the greater stabilizing efficiency of the
N-(RPh)II derivatives relative to that of the phenyl salicylate UV absorber which is a commonly used industrial stabilizer. A radical mechanism is proposed to account for the stabilizing action of the investigated products.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymdegradstab.2006.11.019</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0141-3910 |
ispartof | Polymer degradation and stability, 2007-04, Vol.92 (4), p.733-740 |
issn | 0141-3910 1873-2321 |
language | eng |
recordid | cdi_proquest_miscellaneous_29889395 |
source | ScienceDirect Journals |
subjects | Applied sciences Compounding ingredients Cross-linking Discolouration Exact sciences and technology Organic photo-stabilizers Photo-dehydrochlorination Plasticized poly(vinyl chloride) Polymer industry, paints, wood Stabilization mechanism Stabilizers (antioxydants, antiozonants, etc.) Technology of polymers |
title | N-(Substituted phenyl) itaconimides as organic stabilizers for plasticized poly(vinyl chloride) against photo-degradation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T11%3A17%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=N-(Substituted%20phenyl)%20itaconimides%20as%20organic%20stabilizers%20for%20plasticized%20poly(vinyl%20chloride)%20against%20photo-degradation&rft.jtitle=Polymer%20degradation%20and%20stability&rft.au=Fahmi,%20Mona%20Mohamed&rft.date=2007-04-01&rft.volume=92&rft.issue=4&rft.spage=733&rft.epage=740&rft.pages=733-740&rft.issn=0141-3910&rft.eissn=1873-2321&rft.coden=PDSTDW&rft_id=info:doi/10.1016/j.polymdegradstab.2006.11.019&rft_dat=%3Cproquest_cross%3E29889395%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c394t-dc5bc2a7cfc1cd72e337be297c11b63436de82ff71aef70fd74aa842562e68f03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=29889395&rft_id=info:pmid/&rfr_iscdi=true |