2022
DOI: 10.1016/j.mtchem.2022.101101
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Biomass upcycling of waste rPET to higher-value new-easy-recyclable microcellular thermoplastic (co)polyamide foams and hot-melt adhesives

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Cited by 10 publications
(9 citation statements)
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“…These materials were used to make molecularly complex copoly(ester−amides) through the combination with dimer fatty acid, which were subsequently used to generate hot melt adhesives and foams. 122 Various composites and both epoxy and alkyd resins have been constructed by combining precursors directly with rPET in order to tune mechanics and barrier properties. 123−125 rPET has also been used in non-solvent-induced phase separation to prepare nanoporous membranes for filtration applications.…”
Section: ■ Direct Upcycling To Performance Enhanced Polymeric Materialsmentioning
confidence: 99%
See 1 more Smart Citation
“…These materials were used to make molecularly complex copoly(ester−amides) through the combination with dimer fatty acid, which were subsequently used to generate hot melt adhesives and foams. 122 Various composites and both epoxy and alkyd resins have been constructed by combining precursors directly with rPET in order to tune mechanics and barrier properties. 123−125 rPET has also been used in non-solvent-induced phase separation to prepare nanoporous membranes for filtration applications.…”
Section: ■ Direct Upcycling To Performance Enhanced Polymeric Materialsmentioning
confidence: 99%
“…Very recently, BHET formed as a product of PET depolymerization was converted to phthalamides through aminolysis. These materials were used to make molecularly complex copoly­(ester–amides) through the combination with dimer fatty acid, which were subsequently used to generate hot melt adhesives and foams …”
Section: Direct Upcycling To Performance Enhanced Polymeric Materialsmentioning
confidence: 99%
“…The CO 2 absorption of PA12,36 upsurged as the applied S pressure increased, and reached a peak at 150 bar (at T foaming = 79 °C; F time = 90 min), as displayed in Figure 6 a, which demonstrated that an S pressure of 150 bar was suitable for CO 2 absorption and foaming attributes. The interaction between amide groups in PA12,36 and oxygen groups in CO 2 resulted in a plasticization effect and H-bonds, which augmented the movement of PA12,36 networks and absorbed more CO 2 [ 43 ]. In general, polymeric foams produced at higher S pressure would have smaller cell sizes because more CO 2 is dissolved in the polymer matrix, which affords greater driving energy for cell nucleation compared with lower S pressure and results in more nuclei [ 44 ].…”
Section: Resultsmentioning
confidence: 99%
“…, PET and polylactic acid) mainly due to their lower thermodynamic stability compared to polyolefins. 2,6 The availability of terephthalic acid and its derivatives originating from post-consumer PET serves as a promotor for the development of sustainable thermoplastic 10 and thermosetting polymers. 11–13 Furthermore, their production can use partially depolymerized PET that contains oligomeric byproducts, thus reducing secondary waste generation and lowering energy requirements.…”
Section: Introductionmentioning
confidence: 99%