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

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 chemicall...

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Otros Autores: Rahman, M. Shafiur, Navarathna, Chanaka M., Das, Naba Krishna, Alchouron, Jacinta, Reneau, Parker, Stokes, Sean, Thirumalai, Rooban V. K. G., Pérez, Felio
Formato: Artículo
Lenguaje:Inglés
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Acceso en línea:http://ri.agro.uba.ar/files/intranet/articulo/2021rahman.pdf
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Aporte de:Registro referencial: Solicitar el recurso aquí
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245 1 |a High capacity aqueous phosphate reclamation using Fe/Mg - layered double hydroxide (LDH) dispersed on biochar 
520 |a 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 (CO 2/3- , As 3/4- , SeO2/4- , NO-3,Cr2O2/7, CI-F and Mo2/4) 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. 
650 |2 Agrovoc  |9 26 
653 |a LAYERED DOUBLE HYDROXIDE 
653 |a PHOSPHATE 
653 |a EUTROPHICATION 
653 |a BIOCHAR 
653 |a ADSORPTION 
700 1 |a Rahman, M. Shafiur  |u Mississippi State University. Department of Chemistry. Mississippi State, USA.  |9 22237 
700 1 |9 73848  |a Navarathna, Chanaka M.  |u Mississippi State University. Department of Chemistry. Mississippi State, USA. 
700 1 |a Das, Naba Krishna  |u Mississippi State University. Department of Chemistry. Mississippi State, USA.  |9 73849 
700 1 |9 37868  |a Alchouron, Jacinta  |u Universidad de Buenos Aires. Facultad de Agronomía. Departamento de Recursos Naturales y Ambiente. Cátedra de Botánica General. Buenos Aires, Argentina. 
700 1 |a Reneau, Parker  |u Louisiana Tech University. Department of Chemical Engineering. Ruston, USA.  |9 73850 
700 1 |a Stokes, Sean  |u Mississippi State University. Department of Chemistry. Mississippi State, USA.  |9 73851 
700 1 |a Thirumalai, Rooban V. K. G.  |u Mississippi State University. Institute of Imaging and Analytic Technology. Mississippi State, USA.  |9 73852 
700 1 |9 73853  |a Pérez, Felio  |u University of Memphis. Material Science Lab. Integrated Microscopy Center. Memphis, USA. 
773 |t Journal of colloid and interface science  |g Vol.597 (2021), p.182-195, il., tbls., fot. 
856 |f 2021rahman  |i en reservorio  |q application/pdf  |u http://ri.agro.uba.ar/files/intranet/articulo/2021rahman.pdf  |x ARTI202206 
856 |u https://www.elsevier.com/  |z LINK AL EDITOR 
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