Published May 2021 | Version v1
Journal article

Chemical processes of Cr(VI) removal by Fe-modified biochar under aerobic and anaerobic conditions and mechanism characterization under aerobic conditions using synchrotron-related techniques

  • 1. School of Environmental Studies & State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, 388 Lumo Rd., Wuhan, Hubei 430074 (China)
  • 2. Institute of Ecology and Environmental Governance, College of Life Sciences, Hebei University, Baoding 071002, Hebei Province (China)

Description

Highlights: • Anaerobic rate constant of pseudo-2nd-order model was 3.8 times of aerobic one. • Cr(VI) removal isotherms fit Langmuir (aerobic) and Freundlich (anaerobic) models. • XANES shows Cr in the Fe-modified biochar all existed as Cr(III) form. • EXAFS shows Cr and Fe co-precipitated as FenCr(1−n)(OOH) in Fe-modified biochar. • Removal mechanisms include electrostatic attraction, reduction and co-precipitation. Fe-modified biochar (FeBC) has been considered for aqueous hexavalent chromium (Cr(VI)) removal, but a better understanding is needed with respect to the removal behavior, chemical processes, and removal mechanisms under aerobic and anaerobic conditions. Aqueous Cr(VI) removal was evaluated using unmodified (BC) and FeBC. The Cr(VI) was completely removed in a pH range of 2–10. The removal behavior was properly depicted using pseudo-second-order (PSO) and Langmuir models under aerobic conditions, and using PSO and Freundlich models under anaerobic conditions. Removal rate and capacity were enhanced by up to 3.8 times under anaerobic conditions. Desorption experiments indicated removed Cr in FeBC was stable except under strong acid condition. X-ray absorption spectroscopy (XAS) analysis suggested removed Cr in FeBC was 100% in Cr(III) form and bound to Fe with a bond length of 3.01 Å in the stable form of Fe(III)nCr(III)(1−n)(OOH). The removal mechanisms of Cr(VI) under aerobic conditions by FeBC mainly included electrostatic adsorption, chemical reduction, and complex precipitation.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.scitotenv.2020.144604

Additional details

Identifiers

DOI
10.1016/j.scitotenv.2020.144604;
PII
S0048969720381353;

Publishing Information

Journal Title
Science of the Total Environment
Journal Volume
768
Journal Page Range
vp.
ISSN
0048-9697
CODEN
STENDL

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