2013
DOI: 10.1016/j.polymdegradstab.2013.10.001
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Reactive functionalization of poly(lactic acid), PLA: Effects of the reactive modifier, initiator and processing conditions on the final grafted maleic anhydride content and molecular weight of PLA

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Cited by 91 publications
(108 citation statements)
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References 40 publications
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“…The analysis of the heat flow curves at the first heating scan confirmed that limited variations were observed for the main melting event for samples obtained with the two different techniques, while an additional exothermic peak (a shoulder crystallization peak) that occurs prior to the major melting peak was observed in the case of extruded PLA bionanocomposites. A small melt recrystallization exotherm preceding the main melting endotherm of PLA appears, due to rapid cooling, already reported in He et al [29,30]. The measured values of T g in the case of cast systems, at first heating scan, were lower than glass transition temperatures of extruded samples, due to the presence of residual solvent.…”
Section: Differential Scanning Calorimeter (Dsc)supporting
confidence: 59%
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“…The analysis of the heat flow curves at the first heating scan confirmed that limited variations were observed for the main melting event for samples obtained with the two different techniques, while an additional exothermic peak (a shoulder crystallization peak) that occurs prior to the major melting peak was observed in the case of extruded PLA bionanocomposites. A small melt recrystallization exotherm preceding the main melting endotherm of PLA appears, due to rapid cooling, already reported in He et al [29,30]. The measured values of T g in the case of cast systems, at first heating scan, were lower than glass transition temperatures of extruded samples, due to the presence of residual solvent.…”
Section: Differential Scanning Calorimeter (Dsc)supporting
confidence: 59%
“…Moreover, the residual weight (char yield) obtained at 600°C also gradually increased from 0.02% for E-PLA up to 1.08 and 2.23% for E-PLA/1LNP and E-PLA/3LNP, respectively, due to the chemical structure of lignin, which was demonstrated to weakly contribute to material flammability due to a high charring ability and a low heat release when burning [30]. These positive results could be attributed to the homogeneous dispersion of LNPs in the PLA matrix by using a melt extrusion processing method.…”
Section: Methodsmentioning
confidence: 98%
“…19 Reactive Blending of Binary and Ternary Polymers For producing the binary polymer blends, PLA or PLA-g-MA resins were blended with TPCS resins at a ratio of 70/30 by weight. Details of this modified methodology are described elsewhere.…”
Section: Compounding Of Tpcsmentioning
confidence: 99%
“…However, the D g of MA on the PLA is usually low, e.g., lower than 0.52 wt % [14]. Furthermore, the D g and the grafting parameters were not systematically reported in some literatures.…”
Section: Introductionmentioning
confidence: 97%
“…MA is popular among these grafting pendants due to its difficulty in homopolymerization and the benefit of cell attachment and proliferation [13]. MA was grafted onto PLA by the melt free-radical grafting method with a maximum grafting degree (D g ) of 0.52 wt % [14]. Wu [15] grafted MA onto PLA chains via the solvent free-radical grafting method and the maleated PLA was subsequently used to make PLA-g-MA/green coconut fiber (GCF) blends.…”
Section: Introductionmentioning
confidence: 99%