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Biomass facilitated phase transformation of natural hematite at high temperatures and sorption of Cd2+ and Cu2+

Authors
Wang, ShengsenZhao, MingyueZhou, MinZhao, YitingLi, Yuncong C.Gao, BinFeng, KeYin, WeiqinOk, Yong SikWang, Xiaozhi
Issue Date
Mar-2019
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Heavy metals; Pyrolysis; Iron oxide; Reduction; Ion exchange; Water and wastewater treatment
Citation
ENVIRONMENT INTERNATIONAL, v.124, pp.473 - 481
Indexed
SCIE
SCOPUS
Journal Title
ENVIRONMENT INTERNATIONAL
Volume
124
Start Page
473
End Page
481
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/67183
DOI
10.1016/j.envint.2019.01.004
ISSN
0160-4120
Abstract
Phase changes of natural hematite are often practiced to improve heavy metal removal and magnetism for easy recycling. In this work, pinewood biomass (PB) and natural hematite (H) admixtures were pyrolyzed at 300, 450 and 600 degrees C under N-2 environment to prepare HBC nanocomposites (HBC300, HBC450 and HBC600). The X-ray diffraction (XRD) confirmed the reductive transformation of hematite (crystallite size approximate to 47 nm) into magnetite (25 nm) and further to wustite (25 nm) and zerovalent iron (48 nm). The Langmuir isotherms showed that the maximum sorption capacities of HBC300, HBC450, and HBC600 were 173, 138, and 130 mmol kg(-1) for Cd2+, and 359, 172, and 197 mmol kg(-1) for Cu2+, respectively. The higher pH up to 5 increased sorption of both Cd2+ and Cu2+, whereas the higher ionic strength (0.05-0.4 M) decreased Cd2+ sorption. Sorption of Cd2+ and Cu2+ by HBC300 was accompanied by one order of magnitude greater cation release than HBC450 and HBC600. In a binary system, Cd2+ sorption was depressed by over four times in presence of Cu2+. Overall, ion exchange was more pronounced for HBC300, and Cu2+ was more favorably retained by specific sorption than Cd2+. The greater magnetism of HBC nanoparticles favors separation from aqueous solutions.
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