TY - JOUR
T1 - Selective removal of phosphate using La-porous carbon composites from aqueous solutions
T2 - Batch and column studies
AU - Koilraj, Paulmanickam
AU - Sasaki, Keiko
N1 - Funding Information:
Financial support was provided to KS by Japan Society for Promotion of Science (JSPS) Research Funding (16H02435, 15F15380), and to PK by JSPS Postdoctoral Fellowship for Foreign Researchers (P15380). X-ray photoelectron spectroscopy was performed in Advanced Analytical Center, Kyushu University.
Publisher Copyright:
© 2017 Elsevier B.V.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2017
Y1 - 2017
N2 - Porous carbon composites containing varying La contents were synthesized and studied for the sorption of phosphate. The phosphate sorption capacities increased with increasing La content and showed an almost complete La consumption efficiency (P/La molar ratio of 0.936) for the composite containing a La(OH)3/porous carbon mass ratio of 0.1 (La0.1-PC). Phosphate sorption by these composite materials occurred through precipitation of LaPO4 supported by PXRD, XPS and EDS analyses. Kinetic studies revealed that phosphate sorption by the La0.1-PC composite was rapid and reached equilibrium within 1 h compared to the composites containing higher mass ratio of La(OH)3. The sorption capacity of phosphate was not reduced in the presence 20 mM chloride and 20 mM sulfate, but was disturbed by 20 mM carbonate. The phosphate sorption in the presence of 25 mg/L humic acid was maintained along with the adsorption of dissolved humic acid by electrostatic adsorption onto the carbon support. Interestingly, the phosphate sorption capacity in seawater was twice that in fresh water, likely because the Ca2+ and Mg2+ ions in seawater enhanced the precipitation of phosphate on the surface of La in the La-PC composite. Column experiments verified that the La0.1-PC composite was effective for the continuous treatment of phosphate. The current outcome suggests that the La-PC composite can be used as a multifunctional sorbent for the remediation of phosphate along with alkaline metal ions (Ca2+ and Mg2+) as well as the removal of humic substances in wastewaters. Moreover, the spent sorbent could be repurposed as a phosphate plant fertilizer, where it would reduce the cost of disposal and increase the commercial value.
AB - Porous carbon composites containing varying La contents were synthesized and studied for the sorption of phosphate. The phosphate sorption capacities increased with increasing La content and showed an almost complete La consumption efficiency (P/La molar ratio of 0.936) for the composite containing a La(OH)3/porous carbon mass ratio of 0.1 (La0.1-PC). Phosphate sorption by these composite materials occurred through precipitation of LaPO4 supported by PXRD, XPS and EDS analyses. Kinetic studies revealed that phosphate sorption by the La0.1-PC composite was rapid and reached equilibrium within 1 h compared to the composites containing higher mass ratio of La(OH)3. The sorption capacity of phosphate was not reduced in the presence 20 mM chloride and 20 mM sulfate, but was disturbed by 20 mM carbonate. The phosphate sorption in the presence of 25 mg/L humic acid was maintained along with the adsorption of dissolved humic acid by electrostatic adsorption onto the carbon support. Interestingly, the phosphate sorption capacity in seawater was twice that in fresh water, likely because the Ca2+ and Mg2+ ions in seawater enhanced the precipitation of phosphate on the surface of La in the La-PC composite. Column experiments verified that the La0.1-PC composite was effective for the continuous treatment of phosphate. The current outcome suggests that the La-PC composite can be used as a multifunctional sorbent for the remediation of phosphate along with alkaline metal ions (Ca2+ and Mg2+) as well as the removal of humic substances in wastewaters. Moreover, the spent sorbent could be repurposed as a phosphate plant fertilizer, where it would reduce the cost of disposal and increase the commercial value.
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U2 - 10.1016/j.cej.2017.02.075
DO - 10.1016/j.cej.2017.02.075
M3 - Article
AN - SCOPUS:85013421963
SN - 1385-8947
VL - 317
SP - 1059
EP - 1068
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -