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Sökning: WFRF:(Mankar Smita V.) > (2021)

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1.
  • Guo, Zengwei, et al. (författare)
  • Development of Circularly Recyclable Low Melting Temperature Bicomponent Fibers toward a Sustainable Nonwoven Application
  • 2021
  • Ingår i: ACS Sustainable Chemistry and Engineering. - : American Chemical Society. - 2168-0485. ; 9:49, s. 16778-16785
  • Tidskriftsartikel (refereegranskat)abstract
    • Sustainable low melting temperature bicomponent polyester fibers that can be circularly recycled were developed. The potentially biobased poly(hexamethylene terephthalate) (PHT), acting as the low melting temperature sheath material in the designed bicomponent fibers, was synthesized in a pilot scale. The obtained PHT with an intrinsic viscosity of 0.47 dL/g showed suitable processability when it was processed together with a poly(butylene terephthalate) (PBT) core in a melt-spinning process of bicomponent fibers. Compared with the commercial low melting temperature terephthalate-isophthalate copolyester LMP-160, PHT showed superior mechanical properties according to DMA analysis. The low melting temperature bicomponent fibers with a ratio of the PBT core and PHT sheath at 70:30 were produced smoothly at 290 °C in a pilot melt-spinning line. Preliminary chemical recycling investigations by methanolysis revealed that PHT/PBT bicomponent fibers were completely depolymerized within 2 h at 200 °C, yielding pure terephthalate, which could be conveniently separated and recycled. This indicated the feasibility of circular recycling, which will greatly improve the sustainability of nonwovens thermally bonded by these new bicomponent fibers. © 2021 The Authors. 
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  • Warlin, Niklas, et al. (författare)
  • Synthesis and melt-spinning of partly bio-based thermoplastic poly(cycloacetal-urethane)s toward sustainable textiles
  • 2021
  • Ingår i: Polymer Chemistry. - 1759-9954. ; 12:34, s. 4942-4953
  • Tidskriftsartikel (refereegranskat)abstract
    • A rigid diol with a cyclic acetal structure was synthesized by facile acetalation of fructose-based 5-hydroxymethyl furfural (HMF) and partly bio-based di-trimethylolpropane (di-TMP). This diol (Monomer T) was copolymerized with potentially biobased flexible polytetrahydrofuran and diisocyanates to prepare thermoplastic poly(cycloacetal-urethane)s. A modified one step solution polymerization protocol resulted in relatively high molecular weights (Mn ~ 41.5 -98.9 kDa). All the obtained poly(cycloacetal-urethane)s were amorphous with tuneable glass transition temperatures up to 104 °C. Thermogravimetric analysis indicated that these polymers were thermally stable up to 253 °C and had a relatively high pyrolysis char residue, which may indicate potential inherent flame resistance. Melt rheology measurements were performed to determine a suitable processing window between 165-186 °C, after which the polymer was successfully melt-spun into ~150 meters of homogeneous fibres at 185 °C. The resulting fibres could be readily hydrolysed under acidic conditions, resulting in partialrecovery of the original chemical building blocks.
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  • Resultat 1-7 av 7

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