Mesoporous carbon for efficient removal of microcystin-LR in drinking water sources, Nak-Dong River, South Korea: Application to a field-scale drinking water treatment plant

Authors
Park, Jeong-AnnJung, Sung-MokChoi, Jae-WooKim, Jae-HyunHong, SeungkwanLee, Sang-Hyup
Issue Date
2018-02
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
CHEMOSPHERE, v.193, pp.883 - 891
Abstract
Microcystin-LR (MC-LR) is a growing issue as it is toxic and difficult to remove in drinking water treatment plants (DWTPs). Mesoporous carbon (MC) is evaluated as an alternative adsorbent for MC-LR removal and compared with three widely-used powdered activated carbons (PACs). MC was more favorable for MC-LR removal than PACs. MC-LR adsorption on MC was a rapid process (k(2) = 1.02 x 10(-4) g/mu g/min) that completed within 15 min, while adsorption on PACs took 60 min. The maximum adsorption capacity of MC-LR was 18,008 mu g/g (MC), which was higher than that of the PACs. Two mechanisms were associated with adsorption: the small hydro-dynamic diameter of MC in an aqueous solution increased the instantaneous attraction of MC-LR to its surface, and the numerous mesopores enhanced pore diffusion. The MC could remove MC-LR to meet the drinking water guidance level (1 mu g/L) from an the MC-LR concentration range of 5-20 mu g/L. in drinking water sources, and 10 min of treatment was sufficient to meet this level (MC dose = 20 mg/L). The field-scale DWTP was operated by adding 1 or 5 mg/L MC to the mixing basin, and 49.49% and 74.50% of MC-LR was removed, respectively. Geosmin and 2-methylisoborneol were slightly reduced when 5 mg/L of MC was applied. (C) 2017 Elsevier Ltd. All rights reserved.
Keywords
POWDERED ACTIVATED CARBON; ADVANCED OXIDATION PROCESSES; PHOTOCATALYTIC DESTRUCTION; AQUEOUS-SOLUTIONS; ADSORPTION; CYANOBACTERIA; DEGRADATION; CYANOTOXINS; TOXIN; PRODUCTS; Mesoporous carbon; Cyanobacterial bloom; Microcystin-LR; Pore diffusion; Drinking water treatment plant; Field-scale study
ISSN
0045-6535
URI
https://pubs.kist.re.kr/handle/201004/121762
DOI
10.1016/j.chemosphere.2017.11.092
Appears in Collections:
KIST Article > 2018
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