2009
DOI: 10.1016/j.polymdegradstab.2008.10.004
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Thermal degradation of poly(lactic acid) (PLA) and poly(butylene adipate-co-terephthalate) (PBAT) and their blends upon melt processing

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Cited by 404 publications
(292 citation statements)
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“…The obvious change in initial stage corresponds to the addition of solid materials and their melt. After melting completely, the melt torques of neat PLLA and PLLA/VUB decrease slightly which may be attributed to the shear thinning and possible thermal degradation of the aliphatic polyesters during melting processing [50,51]. It is interesting to find that the PLLA/ VUB/PDLA ternary blends show higher melt torque after melting compared to the PLLA/VUB binary blends, and the torque value increases with increase in the PDLA content.…”
Section: Dynamic Vulcanizationmentioning
confidence: 97%
“…The obvious change in initial stage corresponds to the addition of solid materials and their melt. After melting completely, the melt torques of neat PLLA and PLLA/VUB decrease slightly which may be attributed to the shear thinning and possible thermal degradation of the aliphatic polyesters during melting processing [50,51]. It is interesting to find that the PLLA/ VUB/PDLA ternary blends show higher melt torque after melting compared to the PLLA/VUB binary blends, and the torque value increases with increase in the PDLA content.…”
Section: Dynamic Vulcanizationmentioning
confidence: 97%
“…In the case of intermolecular transesterification, a reaction between two ester molecules exchanges their radicals, thus leading to a variation of the distribution of Mws [140]. Only a few studies considered the intermolecular transesterification [149,150] as a mechanism present during degradation in the melt, which can be minimized by the addition of benzoyl peroxide [151], 1,4-dianthraquinone [152] and other stabilizers. Kopinke et al proposed that above 200°C, PLA can degrade through intra-and intermolecular ester exchange, cis-elimination, radical and concerted non-radical reactions, resulting in the formation of CO, CO 2 , acetaldehyde and methylketene [138,153].…”
Section: Samplementioning
confidence: 99%
“…Doi et al [5] as well as Yu et al [6] argued that thermal and hydrolysis reactions for biocopolymers could be generated by random chain scission reactions of the ester groups following a mathematical model depending on its own composition. Coupled with these two last mechanisms, intra-( Figure 1c) and intermolecular ( Figure 1d) transesterification reactions could also cause a drop in molecular weight at longer reaction times [7,8]. In fact, backbiting effect (zip-like depolymerization, see Figure 1b) leads to the formation of cyclic oligomers (lactide) and lactic acid which is catalyzed by the presence of monomers, oligomers or hydroxyl groups.…”
Section: Introductionmentioning
confidence: 98%