4.7 Article

Characterization of fungal-mediated carbonate precipitation in the biomineralization of chromate and lead from an aqueous solution and soil

Journal

JOURNAL OF CLEANER PRODUCTION
Volume 164, Issue -, Pages 198-208

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jclepro.2017.06.195

Keywords

Biomineralization; Penicillium chrysogenum; Urease; Heavy metals; Calcite

Funding

  1. National Natural Science Foundation of China [41550110499]
  2. National Science and Technology Special Project [2013ZX07310001]

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While microbially induced calcite precipitation (MICP) has been extensively studied by using bacteria for the mineralization of heavy metals, this process is still not completely characterized regarding the remediation of metals from solution and soil using fungi. Thus, in the present study, a ureolytic fungal strain, Penicillium chrysogenum CSI, isolated from cement sludge was, firstly, utilized for the biomineralization of chromate and lead from an aqueous solution. Although this fungal strain immobilized a relatively lower amount of Cr(VI) than Pb in solution, at 200 mg L-1 Pb, fungal-based MICP removed 98.8% of Pb in 12 days. The biomineralization process was characterized by SEM-EDX, which confirmed the typical shape of carbonate crystals precipitated by the fungal strain in addition to the presence of the main elements in the form of metal carbonates. FTIR spectroscopy predicted the functional groups that were responsible for the formation of metal carbonates, while XRD identified biominerals in the form of calcite, vaterite, calcium chromium oxide carbonate and hydrocerussite. Further, when this fungal strain was utilized for metals remediation in soil, an increase in the carbonate-bound fraction of metals in soil was observed. The percentage of exchangeable Cr(VI) decreased from 41.60% to 1.95%, while exchangeable Pb decreased from 41.27% to 2.19% in contaminated soil. This is one of the few studies in which fungal-mediated calcite precipitation is characterized in the remediation of heavy metals. (C) 2017 Elsevier Ltd. All rights reserved.

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