Phosphate removal by anion binding on functionalized nanoporous sorbents.
Phosphate removal by anion binding on functionalized nanoporous sorbents.
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DOI:
10.1021/es100787m
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发表时间:
2010-04-15
影响因子:
11.4
通讯作者:
Yantasee, Wassana
中科院分区:
文献类型:
--
作者:
Chouyyok, Wilaiwan;Wiacek, Robert J.;Pattamakomsan, Kanda;Sangvanich, Thanapon;Grudzien, Rafal M.;Fryxell, Glen E.;Yantasee, Wassana
Phosphate was captured from aqueous solutions by cationic metal-EDA complexes anchored inside mesoporous silica MCM-41 supports (Cu(II)-EDA-SAMMS and Fe(III)-EDA-SAMMS). Fe-EDA-SAMMS was more effective at capturing phosphate than the Cu-EDA-SAMMS and was further studied for matrix effects (e.g., pH, ionic strength, and competing anions) and sorption performance (e.g., capacity and rate). The adsorption of phosphate was highly pH dependent; it increased with increasing pH from 1.0 to 6.5, and decreased above pH 6.5. The adsorption was affected by high ionic strength (0.1 M of NaCl). In the presence of 1000-fold molar excess of chloride and nitrate anions, phosphate removal by Fe-EDA-SAMMS was not affected. Slight, moderate and large impacts were seen with bicarbonate, sulfate and citrate anions, respectively. The phosphate adsorption data on Fe-EDA-SAMMS agreed well with the Langmuir model with the estimated maximum capacity of 43.3 mg/g. The material displayed rapid sorption rate (99% of phosphate removal within 1 min) and lowering the phosphate content to ~ 10 µg/L of phosphorus, which is lower than the EPA’s established freshwater contaminant level for phosphorous (20 µg/L).
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影响因子:
15
作者:
BECK, JS;VARTULI, JC;SCHLENKER, JL
通讯作者:
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56.9
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