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Détail de l'auteur
Auteur Gary L. Bowlin
Documents disponibles écrits par cet auteur
Affiner la rechercheDiblock poly(ester) - poly (ester - ether) copolymers / Nowsheen Goonoo in Industrial & engineering chemistry research, Vol. 51 N° 37 (Septembre 2012)
[article]
in Industrial & engineering chemistry research > Vol. 51 N° 37 (Septembre 2012) . - pp. 12031–12040
Titre : Diblock poly(ester) - poly (ester - ether) copolymers : I. Synthesis, thermal properties, and degradation kinetics Type de document : texte imprimé Auteurs : Nowsheen Goonoo, Auteur ; Archana Bhaw-Luximon, Auteur ; Gary L. Bowlin, Auteur Année de publication : 2012 Article en page(s) : pp. 12031–12040 Note générale : Industrial chemistry Langues : Anglais (eng) Mots-clés : Thermal Properties Kinetics Résumé : The synthesis and characterization of polycaprolactone (PCL) and poly(dioxanone-methyl dioxanone) (P(DX-co-MeDX)) block copolymers in a range of compositions of the two segments and with varying methyl dioxanone units is herein reported. The thermal properties of the copolymers were studied by differential scanning calorimetry (DSC) which revealed that copolymers exhibited two melting transitions ranging between 48 and 53 °C for the PCL segment and 71–79 °C for the P(DX-co-MeDX) segment. Copolymers exhibited only one crystallization exotherm which decreased as the MeDX content of the copolymer increased, thereby increasing miscibility of PCL and P(DX-co-MeDX) segments, a result also confirmed by scanning electron micrographs (SEM). Lastly, the kinetics of thermal degradation of PCL-b-P(DX-co-MeDX) copolymers were investigated by thermogravimetric analysis (TGA). Thermal degradation was shown to proceed in three distinct steps with the P(DX-co-MeDX) segment degrading in the first stage followed by the PCL segment in the last two stages most likely via unzipping and random polymerization mechanisms. The activation energies of copolymer degradation were determined and were found to decrease with increasing MeDX content of the copolymer. Overall, increasing MeDX content influenced both thermal properties and degradation kinetics through phase mixing of segments in the copolymers. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie301703j [article] Diblock poly(ester) - poly (ester - ether) copolymers : I. Synthesis, thermal properties, and degradation kinetics [texte imprimé] / Nowsheen Goonoo, Auteur ; Archana Bhaw-Luximon, Auteur ; Gary L. Bowlin, Auteur . - 2012 . - pp. 12031–12040.
Industrial chemistry
Langues : Anglais (eng)
in Industrial & engineering chemistry research > Vol. 51 N° 37 (Septembre 2012) . - pp. 12031–12040
Mots-clés : Thermal Properties Kinetics Résumé : The synthesis and characterization of polycaprolactone (PCL) and poly(dioxanone-methyl dioxanone) (P(DX-co-MeDX)) block copolymers in a range of compositions of the two segments and with varying methyl dioxanone units is herein reported. The thermal properties of the copolymers were studied by differential scanning calorimetry (DSC) which revealed that copolymers exhibited two melting transitions ranging between 48 and 53 °C for the PCL segment and 71–79 °C for the P(DX-co-MeDX) segment. Copolymers exhibited only one crystallization exotherm which decreased as the MeDX content of the copolymer increased, thereby increasing miscibility of PCL and P(DX-co-MeDX) segments, a result also confirmed by scanning electron micrographs (SEM). Lastly, the kinetics of thermal degradation of PCL-b-P(DX-co-MeDX) copolymers were investigated by thermogravimetric analysis (TGA). Thermal degradation was shown to proceed in three distinct steps with the P(DX-co-MeDX) segment degrading in the first stage followed by the PCL segment in the last two stages most likely via unzipping and random polymerization mechanisms. The activation energies of copolymer degradation were determined and were found to decrease with increasing MeDX content of the copolymer. Overall, increasing MeDX content influenced both thermal properties and degradation kinetics through phase mixing of segments in the copolymers. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie301703j