1997
DOI: 10.1021/ma9520252
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Six-Center Concerted Mechanism for Poly(vinyl chloride) Dehydrochlorination. Requiescat in Pace? Volume 29, Number 23, November 4, 1996, pp 7631−7633

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“…These defects are mainly, allylic or tertiary labile chlorine atoms, which cause the formation of polyenes after losing HCl [5].…”
Section: Introductionmentioning
confidence: 99%
“…These defects are mainly, allylic or tertiary labile chlorine atoms, which cause the formation of polyenes after losing HCl [5].…”
Section: Introductionmentioning
confidence: 99%
“…Aiming at the improvement of this thermal stability, many classes of thermal stabilizers are known, including soap stabilizers (Vymazal et al, 1983;Naqui et al, 1984), organo tin stabilizers and fully organic stabilizers (Banzato et al, 2010;Mohamed and Al-Magribi, 2003;Yassin et al, 1991). Different methods of using these stabilizers are either addition (Sabaa et al, 2005;2006;Abdel-Naby and Al Dossary, 2008a;Abdel-Naby et al, 2010) to the polymer or chemical modification of the polymer to displace the labile sites by more stable stabilizer moieties (Starnes et al, 1997;Abdel-Naby and Youssef, 1998;Abdel-Naby, 1999) Grafting copolymerization (Abdel-Naby 2001;Abdel-Naby and Al Dossary, 2008b) or blending with other polymer (Abdel-Naby and Al Dossary, 2009;Abdel-Naby and El-Hefnawy, 2003) are the most used methods. These last two methods possess the advantage that the stabilizing moieties are polymeric in nature which helps the compatibility between the polymer and the stabilizer moieties as well as the improvement of the mechanical properties (Mohamed and Sabaa, 1999).…”
Section: Introductionmentioning
confidence: 99%