High capacity aqueous phosphate reclamation using Fe/Mg-layered double hydroxide (LDH) dispersed on biochar

[Display omitted] •Fe/Mg-LDH was dispersed on commercial high surface area Douglas fir biochar (LDHBC).•LDHBC phosphate capacity (1279 mg/g) was six-fold greater than LDH (234 mg/g).•1 M NaOH stripped phosphate but reduced following P uptake.•Ion-exchange, chemisorption and precipitation mechanisms...

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Veröffentlicht in:Journal of colloid and interface science 2021-09, Vol.597, p.182-195
Hauptverfasser: Rahman, Sharifur, Navarathna, Chanaka M., Krishna Das, Naba, Alchouron, Jacinta, Reneau, Parker, Stokes, Sean, V.K.G. Thirumalai, Rooban, Perez, Felio, Barbary Hassan, E., Mohan, Dinesh, Pittman, Charles U., Mlsna, Todd
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Sprache:eng
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Zusammenfassung:[Display omitted] •Fe/Mg-LDH was dispersed on commercial high surface area Douglas fir biochar (LDHBC).•LDHBC phosphate capacity (1279 mg/g) was six-fold greater than LDH (234 mg/g).•1 M NaOH stripped phosphate but reduced following P uptake.•Ion-exchange, chemisorption and precipitation mechanisms were considered. Phosphate is a primary plant nutrient, serving integral role in environmental stability. Excessive phosphate in water causes eutrophication; hence, phosphate ions need to be harvested from soil nutrient levels and water and used efficiently. Fe-Mg (1:2) layered double hydroxides (LDH) were chemically co-precipitated and widely dispersed on a cheap, commercial Douglas fir biochar (695 m2/g surface area and 0.26 cm3/g pore volume) byproduct from syn gas production. This hybrid multiphase LDH dispersed on biochar (LDHBC) robustly adsorbed (~5h equilibrium) phosphate from aqueous solutions in exceptional sorption capacities and no pH dependence between pH 1–11. High phosphate Langmuir sorption capacities were found for both LDH (154 to 241 mg/g) and LDH-modified biochar (117 to 1589 mg/g). LDHBC was able to provide excellent sorption performance in the presence of nine competitive anion contaminants (CO32–, AsO43−, SeO42−, NO3–, Cr2O72−, Cl−, F−, SO42−, and MoO42−) and also upon remediating natural eutrophic water samples. Regeneration was demonstrated by stripping with aqueous 1 M NaOH. No dramatic performance drop was observed over 3 sorption-stripping cycles for low concentrations (5 ppm). The adsorbents and phosphate-laden adsorbents were characterized using Elemental analysis, BET, PZC, TGA, DSC, XRD, SEM, TEM, and XPS. The primary sorption mechanism is ion-exchange from low to moderate concentrations (10–500 ppm). Chemisorption and stoichiometric phosphate compound formation were also considered at higher phosphate concentrations (>500 ppm) and at 40 °C. This work advances the state of the art for environmentally friendly phosphate reclamation. These phosphate-laden adsorbents also have potential to be used as a slow-release phosphate fertilizer.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2021.03.114