Radar Absorption Performance of Fe3O4/AC/PANI Nanocomposites Prepared from Natural Iron Sand

被引:6
|
作者
Taufiq, A. [1 ]
Sutiami, R. [1 ]
Subadra, S. U., I [1 ]
Hidayat, A. [1 ]
Diantoro, M. [1 ]
Sunaryono, S. [1 ]
Hidayat, N. [1 ]
Adi, W. A. [2 ]
机构
[1] Univ Negeri Malang, Fac Math & Nat Sci, Dept Phys, Malang, Indonesia
[2] Natl Nucl Energy Agcy, Ctr Technol Nucl Ind Mat, Tangerang, Indonesia
来源
INTERNATIONAL JOURNAL OF ENGINEERING | 2020年 / 33卷 / 02期
关键词
Fe3O4/AC/PANI; Iron Sand; Nanocomposite; Radar Absorbing Material; Simple Coprecipitation Method; ACTIVATED CARBON; FACILE SYNTHESIS; COMPOSITES; NANOPARTICLES; ADSORPTION; POLYANILINE;
D O I
10.5829/ije.2020.33.02b.15
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this work, the Fe3O4 nanoparticles from natural iron sand were combined with active carbon (AC) and polyaniline (PANT) to obtain Fe3O4/AC/PANI nanocomposites with mass variations of the AC of 0.1, 0.2, 0.3, 0.4, and 0.5 g. The crystalline phase of Fe3O4/AC/PANI nanocomposites formed from Fe 3 0 4 with PANI having an amorphous phase. Meanwhile, the crystalline phase of AC was unmatched because of its very small composition. The presence of AC was observed through vibrations from the C-C and COOH functional groups. The existence of PANI was indicated by the vibrations of the benzoic ring and quinonoid bonds. Besides, the presence of Fe3O4 was confirmed by the presence of Fe-O functional groups from octahedral and tetrahedral positions. The optical properties of Fe3O4/AC/PANI nanocomposites were shown by increasing the energy gap along with decreasing absorption wavelength. Interestingly, increasing AC composition made the absorption bandwidth of the Fe3O4/AC/PANI nanocomposites wider, so that the radar absorption also increased marking by the greater reflection loss that reached -15.8 dB. The increase in the radar absorption performance of Fe3O4/AC/PANI nanocomposites came from the efficient complementarity between dielectric loss and magnetic loss and interfacial polarization between Fe3O4-AC or between Fe3O4-PANI.
引用
收藏
页码:304 / 313
页数:10
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