Enhanced removal of phosphate from aqueous solutions using a modified sludge derived biochar: Comparative study of various modifying cations and RSM based optimization of pyrolysis parameters

Different biochars produced by the impregnation of Mg, Ca, Al, Cu, and Fe were compared for the phosphate (P) uptake capacity and the effect on solution pH. Among them, Ca- and Mg-rich biochars demonstrate better sorption ability to P and have less effect on pH change. The optimum conditions of the...

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Veröffentlicht in:Journal of environmental management 2018-11, Vol.225, p.75-83
Hauptverfasser: Saadat, Solmaz, Raei, Ehsan, Talebbeydokhti, Nasser
Format: Artikel
Sprache:eng
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Zusammenfassung:Different biochars produced by the impregnation of Mg, Ca, Al, Cu, and Fe were compared for the phosphate (P) uptake capacity and the effect on solution pH. Among them, Ca- and Mg-rich biochars demonstrate better sorption ability to P and have less effect on pH change. The optimum conditions of the pyrolysis processes were determined using response surface methodology. Comparison of the P removal efficiency of these two biochars under optimum conditions imply the superior adsorption capability of Ca-rich biochar. According to XRD analysis, calcite is the dominant mineral on the biochar surface, indicating the potential of Ca-rich biochar for P removal by adsorption and precipitation. Predictive second-order kinetic and linear Langmuir isotherm models could adequately interpret the P sorption process for optimized Ca-rich biochar. The maximum P sorption capacity of Ca-rich biochar of 153.85 mg/g is superior to other adsorbents reported in literature. [Display omitted] •Ca-rich biochar had better P sorption ability and exerted less effect on pH change.•RSM based optimized Ca-rich biochar showed high P removal capacity of 153.85 mg/g.•Pure calcite is the dominant mineral on the Ca-rich biochar surface.•Smooth kinetics imply the less significant role of precipitation in P removal.•Dependency of sorption on t0.5 shows the significance of intra-particle diffusion.
ISSN:0301-4797
1095-8630
DOI:10.1016/j.jenvman.2018.07.037