2016
DOI: 10.1016/j.eurpolymj.2016.08.004
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Production of bio-based 2,5-furan dicarboxylate polyesters: Recent progress and critical aspects in their synthesis and thermal properties

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Cited by 387 publications
(337 citation statements)
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“…As shown in Table 1, the actual composition of the resultant copolyester could be controlled by the feed ratio of FDCA to CL mono mers. The PDI is among 2.11 to 3.49 and the broad polymer diversity is ascribed to the existence of impurities in bio-based FDCA and decarboxylation of 2,5-FDCA under reaction conditions [13]. The weigh-average molecular weights of obtained PBFCL samples are among 8.05 to 40.7 kg/mol.…”
Section: Characterizationmentioning
confidence: 86%
See 1 more Smart Citation
“…As shown in Table 1, the actual composition of the resultant copolyester could be controlled by the feed ratio of FDCA to CL mono mers. The PDI is among 2.11 to 3.49 and the broad polymer diversity is ascribed to the existence of impurities in bio-based FDCA and decarboxylation of 2,5-FDCA under reaction conditions [13]. The weigh-average molecular weights of obtained PBFCL samples are among 8.05 to 40.7 kg/mol.…”
Section: Characterizationmentioning
confidence: 86%
“…They were random copolymers whose composition was well controlled by the feed ratio of the diacid monomers. The ability of the copolymer to crystallize was drastically reduced with the addition of the comonomer and consequently increase of the elongation at break of the polymer [13]. These FDCA based polyesters have shown great prospective to replace their petroleumbased counterparts applied as plastic products [3,8].…”
Section: Introductionmentioning
confidence: 98%
“…These include, among others, 2,5-furanedicarboxylic acid (FDCA) synthesized from 5-hydroxymethylfurfural (HMF) [7]. It was identified as one of the twelve most promising compounds of vegetal origin for the synthesis of polymeric materials including polyurethanes, polyamides and polyesters [2,4,5,8,9] as well as their copolymers with elastomeric properties.…”
mentioning
confidence: 99%
“…It was identified as one of the twelve most promising compounds of vegetal origin for the synthesis of polymeric materials including polyurethanes, polyamides and polyesters [2,4,5,8,9] as well as their copolymers with elastomeric properties. Polyesters that contain furan moieties in their structures, have been widely investigated for decades, starting with Moore and Kelly's pioneering research about thirty years ago [10] and continuing with some recent studies [7,[11][12][13]. Nevertheless, the synthesis of the furan homologue of poly (ethylene terephthalate) (PET), i.e.…”
mentioning
confidence: 99%
“…It is produced industrially via dehydration of sorbitol, the latter being obtained by hydrogenation of glucose. Isosorbide is also a good candidate for the replacement of bisphenol A, which is toxic, and has also gained high importance in recent years for the production of novel materials for food packaging applications, like furanoate polyesters [7][8][9][10]. An important drawback must however be tackled when considering its insertion into PET.…”
Section: Introductionmentioning
confidence: 99%