Heavy metal sorption by sludge-derived biochar with focus on Pb2+ sorption capacity at µg/L concentrations Show others and affiliations
2020 (English) In: Processes, ISSN 2227-9717, Vol. 8, no 12, p. 1-23, article id 1559Article in journal (Refereed) Published
Abstract [en]
Municipal wastewater management causes metal exposure to humans and the environment. Targeted metal removal is suggested to reduce metal loads during sludge reuse and release of effluent to receiving waters. Biochar is considered a low-cost sorbent with high sorption capacity for heavy metals. In this study, heavy metal sorption to sludge-derived biochar (SDBC) was investigated through batch experiments and modeling and compared to that of wood-derived biochar (WDBC) and activated carbon (AC). The aim was to investigate the sorption efficiency at metal concentrations comparable to those in municipal wastewater (<1 mg/L), for which experimental data are lacking and isotherm models have not been verified in previous works. Pb2+ removal of up to 83% was demonstrated at concentrations comparable to those in municipal wastewater, at pH 2. SDBC showed superior Pb2+ sorption capacity (maximum ~2 mg/g at pH 2) compared to WDBC and AC (<0 and (3.5 ± 0.4) × 10−3 mg/g, respectively); however, at the lowest concentration investigated (0.005 mg/L), SDBC released Pb2+. The potential risk of release of other heavy metals (i.e., Ni, Cd, Cu, and Zn) needs to be further examined. The sorption capacity of SDBC over a metal concentration span of 0.005–150 mg Pb2+/L could be predicted with the Redlich– Peterson model. It was shown that experimental data at concentrations comparable to those in municipal wastewater are necessary to accurately model and predict the sorption capacity of SDBC at these concentrations.
Place, publisher, year, edition, pages MDPI AG , 2020. Vol. 8, no 12, p. 1-23, article id 1559
Keywords [en]
Adsorbent, Biosorbent, Heavy metals, Isotherm models, Municipal wastewater, Sewage treatment
National Category
Engineering and Technology
Identifiers URN: urn:nbn:se:ri:diva-72391 DOI: 10.3390/pr8121559 Scopus ID: 2-s2.0-85097001940 OAI: oai:DiVA.org:ri-72391 DiVA, id: diva2:1846667
2024-03-252024-03-252024-04-02 Bibliographically approved