• 文献标题:   Secondary recycled acrylonitrile-butadiene-styrene and graphene composite for 3D/4D applications: Rheological, thermal, magnetometric, and mechanical analyses
  • 文献类型:   Article, Early Access
  • 作  者:   KUMAR V, SINGH R, AHUJA IPS
  • 作者关键词:   recycled abs, graphene, dsc, vsm, sem, eds analysi
  • 出版物名称:   JOURNAL OF THERMOPLASTIC COMPOSITE MATERIALS
  • ISSN:   0892-7057 EI 1530-7980
  • 通讯作者地址:   Guru Nanak Dev Engn Coll
  • 被引频次:   0
  • DOI:   10.1177/0892705720925114 EA MAY 2020
  • 出版年:  

▎ 摘  要

This study reports investigation on nano-sized (5-10 nm) graphene (Gr)-reinforced, secondary (2 degrees) recycled acrylonitrile-butadiene-styrene (ABS) as a smart composite material for 3D and 4D applications. Gr was blended (in different weight proportions) with 2 degrees-recycled ABS granules mechanically for selection of composition/proportion after ascertaining rheological property (based upon melt flow index according to ASTM D 1238), thermal stability based upon differential scanning calorimetry, and magnetic property based upon vibration sample magnetometry. The selected compositions/proportions of ABS-Gr composite was further processed with a twin-screw extruder by varying screw temperature and torque. The results of the study suggest that as regards to mechanical properties (peak strength and Shore D hardness) are concerned, the best settings are 20 wt% Gr reinforcement in ABS at a screw temperature 210 degrees C with torque of 0.4 Nm. The corresponding heat capacity and magnetization for the selected composition/proportion was observed as 0.77 J/g and 0.10 x 10(-5) emu (+magnetization), 0.080 x 10(-5) emu (-magnetization), respectively. The coercivity of the selected compositions ranges from 79.19 Oe to 1260.34 Oe (+coercivity) and 4.64 Oe to 639.50 Oe (-coercivity), whereas the retentivity of the investigated compositions ranges from 2.36 x 10(-5) G to 5.44 x 10(-4) G (+retentivity) and 4.31 x 10(-5) G to 3.48 x 10(-5) G (-retentivity). The results have been counter verified based upon optical photo micrographs, porosity analysis, scanning electron microscopy analysis, and energy-dispersive spectroscopy analysis.