| Literature DB >> 22078228 |
Min Ma1, Ruiping Liu, Huijuan Liu, Jiuhui Qu.
Abstract
This study developed a novel KMnO(4)-Fe(II) process to remove the cells of Microcystis aeruginosa, and the mechanisms involved in have been investigated. At KMnO(4) doses of 0-10.0 μM, the KMnO(4)-Fe(II) process showed 23.4-53.3% higher efficiency than the KMnO(4)-Fe(III) process did. This was first attributed to the moderate pre-oxidation of M. aeruginosa by KMnO(4), achieved by dosing Fe(II) after a period of pre-oxidation, to cease the further release of intracellular organic matter (IOM) and the degradation of dissolved organic matter (DOM). The extensive exposure of M. aeruginosa to KMnO(4) in KMnO(4)-Fe(III) process led to high levels and insufficient molecular weight of DOM, inhibiting the subsequent Fe(III) coagulation. Additionally, Fe(II) contributed to lower levels of the in-situ formed MnO(2), the reduction product of KMnO(4) which adversely affected algae removal by Fe(III) coagulation. However, the in-situ formed Fe(III), which was derived from the oxidation of Fe(II) by KMnO(4), in-situ MnO(2), and dissolved oxygen, dominated the remarkably high efficiency of KMnO(4)-Fe(II) process with respect to the removal of M. aeruginosa. On one hand, in-situ formed Fe(III) had more reactive surface area than pre-formed Fe(III). On the other hand, the continuous introduction of fresh Fe(III) coagulant showed higher efficiency than one-off dosage of coagulant to destabilize M. aeruginosa cells and to increase the flocs size. Moreover, the MnO(2) precipitated on algae cell surfaces and contributed to the formation of in-situ formed Fe(III), which may act as bridges to enhance the removal of M. aeruginosa.Entities:
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Year: 2011 PMID: 22078228 DOI: 10.1016/j.watres.2011.10.022
Source DB: PubMed Journal: Water Res ISSN: 0043-1354 Impact factor: 11.236