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    Heat-treated biochar impregnated with zero-valent iron nanoparticles for organic contaminants removal from aqueous phase: Material characterizations and kinetic studies

    Year: 2019

    Journal: J. Ind. Eng. Chem., Volume 76, AUG 25, page 197–214

    Authors: Mortazavian, Soroosh; Jones-Lepp, Tammy; Bae, Jee-Hwan; Chun, Dongwon; Bandala, Erick R.; Moon, Jaeyun

    Organizations: U.S. Department of Energy Minority-Serving Institution Partnership Program (MSIPP)United States Department of Energy (DOE) [000033-29-78]

    Keywords: Biochar modification; Hydrophilic biochar; Surface functional groups; p-nitrosodimethylaniline (RNO); Pore structure analysis; Trichloroethylene (TCE) degradation

    Biochar (BC) is an inexpensive and widely available carbon-based material with a variety of applications. Zero valent iron nanoparticles (nZVI), on the other hand, are highly reactive species. However, agglomeration and difficulty of separation from the treated media are the major reported drawbacks associated with nZVI application for water treatment. In this study, BC was modified by a simple heat treatment, producing hydrophilic heat-treated biochar (HBC) with enhanced absorptive features, and was impregnated with nZVI, producing BC/nZVI composite for efficient organic contaminant removal. Synthesis conditions of BC/nZVI composite were optimized by evaluating p-nitrosodimethylaniline (pNDA) bleaching efficiency of various BC/nZVI samples synthesized under different conditions of pH, ultrasonication amplitude, and iron concentration. Variously-synthesized HBCs were then used to synthesize HBC/nZVI composites, and were characterized for surface morphology, surface chemistry, and elemental composition. The best-performing HBC/nZVI for pNDA bleaching was then used for trichloroethylene (TCE) removal from water. Using HBC/nZVI or BC/nZVI composites, the pseudo second order model fit indicated a chemisorption mechanism for organic contaminants removal. Using 250 mg L-1 of the best-performing HBC/nZVI, an 88% TCE reduction (initial concentration of 40 mu g L-1) was achieved after 20 min at pH = 3.0, with a rate of 3.318 g mg(-1) min(-1). (C) 2019 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
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