Abstract
The chemical and physical properties of 20 biochars produced at 350, 450, 550 and 650 °C were investigated to determine the key roles they play in the sorption and desorption of three potentially toxic elements (Pb, Cd, As). Biochar surfaces were studied using scanning electron microscopy, Fourier transform infra-red spectroscopy, X-ray diffraction and X-ray photoelectron spectroscopy. Organic functional groups (e.g. single bondCOOH, Cdouble bond; length as m-dashO, Csingle bondX), inorganic minerals (CaCO3, SiO2, Ca2Si5O10·3H2O) and cations (K+, Ca2+, Mg2+, Na+) controlled PTE sorption significantly while physical properties (morphology, surface area) showed little influence on the sorption of potentially toxic elements. Four major mechanisms accounted for the exceptionally high Pb(II) sorption by all 20 biochars (97.5–99.8%) while Cd(II) and As(III) sorption (<90% and 42% respectively) were controlled by two mechanisms (precipitation and electrostatic attraction) only. Thermodynamic studies suggested that Pb and Cd sorption on a majority of biochars was spontaneous and endothermic while As sorption was also endothermic but not spontaneous. Sorbed PTEs were observed to be very stable over a wide range of pH values (3.5–9.5) with desorption ranging from 0.2 - 16.5%. Detailed understanding of how biochar surface properties interact with PTEs increases the possibility of developing cost effective and engineered biochars with exceptional sorption characteristics.
Original language | English |
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Pages (from-to) | 127–136 |
Journal | Journal of Cleaner Production |
Volume | 148 |
Early online date | 25 Jan 2017 |
DOIs | |
Publication status | Published - 1 Apr 2017 |
Keywords
- Biochar property
- Sorption capacity
- Potentially toxic element
- pH
Profiles
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Brian Reid
- School of Environmental Sciences - Professor of Soil Science
- Centre for Ecology, Evolution and Conservation - Member
- Environmental Biology - Member
- Geosciences - Member
Person: Research Group Member, Research Centre Member, Academic, Teaching & Research