Organic thermal stabilizers for rigid poly(vinyl chloride) I. Barbituric and thiobarbituric acids

Barbituric acid (BA) and thiobarbituric acid (TBA) have been investigated as thermal stabilizers for rigid poly(vinyl chloride) (PVC) at 180°C, in air. The efficiency of these compounds as thermal stabilizers was evaluated by measuring the length of the induction period ( T s), during which no detec...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Polymer degradation and stability 2000-01, Vol.70 (1), p.5-10
Hauptverfasser: Mohamed, N.A., Yassin, A.A., Khalil, Kh.D., Sabaa, M.W.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 10
container_issue 1
container_start_page 5
container_title Polymer degradation and stability
container_volume 70
creator Mohamed, N.A.
Yassin, A.A.
Khalil, Kh.D.
Sabaa, M.W.
description Barbituric acid (BA) and thiobarbituric acid (TBA) have been investigated as thermal stabilizers for rigid poly(vinyl chloride) (PVC) at 180°C, in air. The efficiency of these compounds as thermal stabilizers was evaluated by measuring the length of the induction period ( T s), during which no detectable amount of hydrogen chloride gas could be observed, and also from the rate of dehydrochlorination as measured by continuous potentiometric titration on one hand, and the extent of discoloration of the degraded polymer on the other. The stabilizing efficiencies were compared with that of dibasic lead carbonate (DBLC), dibasic lead stearate (DBLS), barium–cadmium–zinc stearate (Ba–Cd–Zn stearate), n-octyl tin mercaptide ( n-OTM) and dibutyl tin maleate (DBTM). With the exception of DBTM reference stabilizer which shows a comparable stabilizing efficiency with BA and TBA, the investigated organic stabilizers exhibit a greater efficiency than those of all other reference stabilizers. Moreover, they impart better color stability to the degraded samples. A radical mechanism for the stabilizing action is suggested. The stabilizing efficiency is attributed to the replacement of the labile chlorine atoms on the PVC chains by a relatively more stable moiety of the stabilizer. This disrupts the formation of conjugated double bonds, which are responsible for the discoloration.
doi_str_mv 10.1016/S0141-3910(00)00054-9
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_27689265</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0141391000000549</els_id><sourcerecordid>27689265</sourcerecordid><originalsourceid>FETCH-LOGICAL-c367t-f5d8369765e9d82a36b3629fb7658e2be673647a9fc5331dde4a56196b47aba93</originalsourceid><addsrcrecordid>eNqFkE9LxDAQxYMouK5-BKEHkfVQTZombU6ii38WBA_qOaTJVEey7Zp0hfXTm3VFvQkDA4_fvMc8Qg4ZPWWUybMHykqWc8XohNITSqkoc7VFRqyueF7wgm2T0Q-yS_ZifE0QLQUbEXMfnk2HNhteIMyNz-JgGvT4ASFmbR-ygM_oskXvV5N37FY-sy--D-jgJJudZpcmNDgsQzIwnUsm2Dd_JIsu7pOd1vgIB997TJ6urx6nt_nd_c1senGXWy6rIW-Fq7lUlRSgXF0YLhsuC9U2SamhaEBWXJaVUa0VnDPnoDRCMiWbJDZG8TE53vguQv-2hDjoOUYL3psO-mXURSVrVUiRQLEBbehjDNDqRcC5CSvNqF4Xqr8K1eu2NF1PKlSvA46-A0y0xrfBdBbj77Eoai5ows43GKRn3xGCjhahs-AwgB206_GfoE_gAYoh</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>27689265</pqid></control><display><type>article</type><title>Organic thermal stabilizers for rigid poly(vinyl chloride) I. Barbituric and thiobarbituric acids</title><source>Elsevier ScienceDirect Journals</source><creator>Mohamed, N.A. ; Yassin, A.A. ; Khalil, Kh.D. ; Sabaa, M.W.</creator><creatorcontrib>Mohamed, N.A. ; Yassin, A.A. ; Khalil, Kh.D. ; Sabaa, M.W.</creatorcontrib><description>Barbituric acid (BA) and thiobarbituric acid (TBA) have been investigated as thermal stabilizers for rigid poly(vinyl chloride) (PVC) at 180°C, in air. The efficiency of these compounds as thermal stabilizers was evaluated by measuring the length of the induction period ( T s), during which no detectable amount of hydrogen chloride gas could be observed, and also from the rate of dehydrochlorination as measured by continuous potentiometric titration on one hand, and the extent of discoloration of the degraded polymer on the other. The stabilizing efficiencies were compared with that of dibasic lead carbonate (DBLC), dibasic lead stearate (DBLS), barium–cadmium–zinc stearate (Ba–Cd–Zn stearate), n-octyl tin mercaptide ( n-OTM) and dibutyl tin maleate (DBTM). With the exception of DBTM reference stabilizer which shows a comparable stabilizing efficiency with BA and TBA, the investigated organic stabilizers exhibit a greater efficiency than those of all other reference stabilizers. Moreover, they impart better color stability to the degraded samples. A radical mechanism for the stabilizing action is suggested. The stabilizing efficiency is attributed to the replacement of the labile chlorine atoms on the PVC chains by a relatively more stable moiety of the stabilizer. This disrupts the formation of conjugated double bonds, which are responsible for the discoloration.</description><identifier>ISSN: 0141-3910</identifier><identifier>EISSN: 1873-2321</identifier><identifier>DOI: 10.1016/S0141-3910(00)00054-9</identifier><identifier>CODEN: PDSTDW</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Compounding ingredients ; Discoloration ; Exact sciences and technology ; Organic thermal stabilizers ; Poly(vinyl chloride) ; Polymer industry, paints, wood ; Stabilization mechanism ; Stabilizers (antioxydants, antiozonants, etc.) ; Technology of polymers ; Thermal dehydrochlorination</subject><ispartof>Polymer degradation and stability, 2000-01, Vol.70 (1), p.5-10</ispartof><rights>2000 Elsevier Science Ltd</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-f5d8369765e9d82a36b3629fb7658e2be673647a9fc5331dde4a56196b47aba93</citedby><cites>FETCH-LOGICAL-c367t-f5d8369765e9d82a36b3629fb7658e2be673647a9fc5331dde4a56196b47aba93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0141-3910(00)00054-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1528350$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Mohamed, N.A.</creatorcontrib><creatorcontrib>Yassin, A.A.</creatorcontrib><creatorcontrib>Khalil, Kh.D.</creatorcontrib><creatorcontrib>Sabaa, M.W.</creatorcontrib><title>Organic thermal stabilizers for rigid poly(vinyl chloride) I. Barbituric and thiobarbituric acids</title><title>Polymer degradation and stability</title><description>Barbituric acid (BA) and thiobarbituric acid (TBA) have been investigated as thermal stabilizers for rigid poly(vinyl chloride) (PVC) at 180°C, in air. The efficiency of these compounds as thermal stabilizers was evaluated by measuring the length of the induction period ( T s), during which no detectable amount of hydrogen chloride gas could be observed, and also from the rate of dehydrochlorination as measured by continuous potentiometric titration on one hand, and the extent of discoloration of the degraded polymer on the other. The stabilizing efficiencies were compared with that of dibasic lead carbonate (DBLC), dibasic lead stearate (DBLS), barium–cadmium–zinc stearate (Ba–Cd–Zn stearate), n-octyl tin mercaptide ( n-OTM) and dibutyl tin maleate (DBTM). With the exception of DBTM reference stabilizer which shows a comparable stabilizing efficiency with BA and TBA, the investigated organic stabilizers exhibit a greater efficiency than those of all other reference stabilizers. Moreover, they impart better color stability to the degraded samples. A radical mechanism for the stabilizing action is suggested. The stabilizing efficiency is attributed to the replacement of the labile chlorine atoms on the PVC chains by a relatively more stable moiety of the stabilizer. This disrupts the formation of conjugated double bonds, which are responsible for the discoloration.</description><subject>Applied sciences</subject><subject>Compounding ingredients</subject><subject>Discoloration</subject><subject>Exact sciences and technology</subject><subject>Organic thermal stabilizers</subject><subject>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><subject>Thermal dehydrochlorination</subject><issn>0141-3910</issn><issn>1873-2321</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkE9LxDAQxYMouK5-BKEHkfVQTZombU6ii38WBA_qOaTJVEey7Zp0hfXTm3VFvQkDA4_fvMc8Qg4ZPWWUybMHykqWc8XohNITSqkoc7VFRqyueF7wgm2T0Q-yS_ZifE0QLQUbEXMfnk2HNhteIMyNz-JgGvT4ASFmbR-ygM_oskXvV5N37FY-sy--D-jgJJudZpcmNDgsQzIwnUsm2Dd_JIsu7pOd1vgIB997TJ6urx6nt_nd_c1senGXWy6rIW-Fq7lUlRSgXF0YLhsuC9U2SamhaEBWXJaVUa0VnDPnoDRCMiWbJDZG8TE53vguQv-2hDjoOUYL3psO-mXURSVrVUiRQLEBbehjDNDqRcC5CSvNqF4Xqr8K1eu2NF1PKlSvA46-A0y0xrfBdBbj77Eoai5ows43GKRn3xGCjhahs-AwgB206_GfoE_gAYoh</recordid><startdate>20000101</startdate><enddate>20000101</enddate><creator>Mohamed, N.A.</creator><creator>Yassin, A.A.</creator><creator>Khalil, Kh.D.</creator><creator>Sabaa, M.W.</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>20000101</creationdate><title>Organic thermal stabilizers for rigid poly(vinyl chloride) I. Barbituric and thiobarbituric acids</title><author>Mohamed, N.A. ; Yassin, A.A. ; Khalil, Kh.D. ; Sabaa, M.W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-f5d8369765e9d82a36b3629fb7658e2be673647a9fc5331dde4a56196b47aba93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Applied sciences</topic><topic>Compounding ingredients</topic><topic>Discoloration</topic><topic>Exact sciences and technology</topic><topic>Organic thermal stabilizers</topic><topic>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><topic>Thermal dehydrochlorination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohamed, N.A.</creatorcontrib><creatorcontrib>Yassin, A.A.</creatorcontrib><creatorcontrib>Khalil, Kh.D.</creatorcontrib><creatorcontrib>Sabaa, M.W.</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>Mohamed, N.A.</au><au>Yassin, A.A.</au><au>Khalil, Kh.D.</au><au>Sabaa, M.W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Organic thermal stabilizers for rigid poly(vinyl chloride) I. Barbituric and thiobarbituric acids</atitle><jtitle>Polymer degradation and stability</jtitle><date>2000-01-01</date><risdate>2000</risdate><volume>70</volume><issue>1</issue><spage>5</spage><epage>10</epage><pages>5-10</pages><issn>0141-3910</issn><eissn>1873-2321</eissn><coden>PDSTDW</coden><abstract>Barbituric acid (BA) and thiobarbituric acid (TBA) have been investigated as thermal stabilizers for rigid poly(vinyl chloride) (PVC) at 180°C, in air. The efficiency of these compounds as thermal stabilizers was evaluated by measuring the length of the induction period ( T s), during which no detectable amount of hydrogen chloride gas could be observed, and also from the rate of dehydrochlorination as measured by continuous potentiometric titration on one hand, and the extent of discoloration of the degraded polymer on the other. The stabilizing efficiencies were compared with that of dibasic lead carbonate (DBLC), dibasic lead stearate (DBLS), barium–cadmium–zinc stearate (Ba–Cd–Zn stearate), n-octyl tin mercaptide ( n-OTM) and dibutyl tin maleate (DBTM). With the exception of DBTM reference stabilizer which shows a comparable stabilizing efficiency with BA and TBA, the investigated organic stabilizers exhibit a greater efficiency than those of all other reference stabilizers. Moreover, they impart better color stability to the degraded samples. A radical mechanism for the stabilizing action is suggested. The stabilizing efficiency is attributed to the replacement of the labile chlorine atoms on the PVC chains by a relatively more stable moiety of the stabilizer. This disrupts the formation of conjugated double bonds, which are responsible for the discoloration.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/S0141-3910(00)00054-9</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0141-3910
ispartof Polymer degradation and stability, 2000-01, Vol.70 (1), p.5-10
issn 0141-3910
1873-2321
language eng
recordid cdi_proquest_miscellaneous_27689265
source Elsevier ScienceDirect Journals
subjects Applied sciences
Compounding ingredients
Discoloration
Exact sciences and technology
Organic thermal stabilizers
Poly(vinyl chloride)
Polymer industry, paints, wood
Stabilization mechanism
Stabilizers (antioxydants, antiozonants, etc.)
Technology of polymers
Thermal dehydrochlorination
title Organic thermal stabilizers for rigid poly(vinyl chloride) I. Barbituric and thiobarbituric acids
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T06%3A24%3A39IST&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=Organic%20thermal%20stabilizers%20for%20rigid%20poly(vinyl%20chloride)%20I.%20Barbituric%20and%20thiobarbituric%20acids&rft.jtitle=Polymer%20degradation%20and%20stability&rft.au=Mohamed,%20N.A.&rft.date=2000-01-01&rft.volume=70&rft.issue=1&rft.spage=5&rft.epage=10&rft.pages=5-10&rft.issn=0141-3910&rft.eissn=1873-2321&rft.coden=PDSTDW&rft_id=info:doi/10.1016/S0141-3910(00)00054-9&rft_dat=%3Cproquest_cross%3E27689265%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=27689265&rft_id=info:pmid/&rft_els_id=S0141391000000549&rfr_iscdi=true