4.7 Article

Hydrophobic, UV resistant and dielectric polyurethane-nanolignin composites with good reprocessability

期刊

MATERIALS & DESIGN
卷 196, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.matdes.2020.109150

关键词

Polyurethane; Lignin nanoparticle; Hydrophobicity; UV resistance; Dielectric behavior

资金

  1. National Science Foundation of China [51903106, 51873082]
  2. Key Laboratory of Bio-basedMaterial Science & Technology (Northeast Forestry University), Ministry of Education [SWZ-ZD201904]
  3. Fundamental Research Funds for the Central Universities [JUSRP11928]
  4. MOE & SAFEA 111 Project [B13025]

向作者/读者索取更多资源

Lignin nanoparticles (LNP) were obtained by an acidolysis process from corn pristine lignin. X-ray photoelectron spectroscopy (XPS) and radical scavenging activity (RSA) of the free radical 2,2-diphenyl-1-picrylhydrazyl (DPPH) confirmed a significant enhancement in reactivity of LNP in comparison with pristine lignin. Polyurethane (PU) nanocomposites were prepared by pre-polymerization of polyethylene glycol and diisocyanates the presence of different contents (1, 3, 5 and 7 wt%) of LNP. The effects of LNP, serving as both biobased polyol and crosslinker, on the mechanical, hydrophobicity and dielectric behavior of the resulted PU nanocomposites were investigated. Tensile test results showed an overall enhancement for mechanical performance, and elongation at break exceeded 1000% for all studied PU nanocomposites. Meanwhile, dynamic mechanical analysis (DMA) revealed that the crosslinking densities gradually increased with LNP addition. Furthermore, based PU nanocomposites showed inherent resistance towards ultraviolet radiation and frequency dependent behavior for electrical conductivity. On the other hand, LNP based PU nanocomposites revealed good thermal reprocessability due to the transcarbamoylation reaction in the presence of DBTDL catalyst. (c) 2020 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).

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