Novel Microwave Absorber of Ni Mn FeO/Carbonized Chaff ( = 0.3, 0.5, and 0.7) Based on Biomass.

ACS Omega

College of Science and College of Mechanical and Electrical Engineering, Sichuan Agricultural University, Ya'an 625014, P. R. China.

Published: July 2019

AI Article Synopsis

  • A novel magnetic nanocomposite of NiMnFeO/carbonized chaff has been synthesized using co-carbonization and hydrothermal methods.
  • The composite demonstrated superior microwave absorption properties, achieving a maximum reflection loss of -14.58 dB at 1.91 GHz with a significant bandwidth of 0.95 GHz.
  • This study highlights an innovative approach to creating effective and eco-friendly electromagnetic wave absorbers by leveraging renewable biomaterials.

Article Abstract

A novel magnetic nanocomposite of Ni Mn FeO/carbonized chaff ( = 0.3, 0.5, and 0.7) has been synthesized successfully via the co-carbonization and hydrothermal method. The microstructure, morphology, complex permittivity and permeability, and microwave absorbing properties were systematically studied by X-ray diffraction, scanning electron microscopy, and a vector network analyzer. Compared to the pure NiMnFeO NPs, the NiMnFeO/carbonized chaff-N composite exhibits an optimal microwave absorption property at 4 mm as the mass percent of carbonized chaff is 10 wt %, the maximum reflection loss of which can reach -14.58 dB at 1.91 GHz with the -10 dB frequency bandwidth in the range of 1.46-2.41 GHz (0.95 GHz). The enhanced electromagnetic wave absorbing performance is ascribed to the good synergistic effect among laminated structures, better impedance matching condition, strong natural resonance loss, Debye dipolar relaxation to some extent, and so forth. Most importantly, this study provides a novel way to prepare easily degradable, environment-friendly, and high-efficiency electromagnetic wave absorbers by utilizing the structural property of renewable biomaterials.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682147PMC
http://dx.doi.org/10.1021/acsomega.9b01568DOI Listing

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