Journal
JOURNAL OF HAZARDOUS MATERIALS
Volume 422, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.jhazmat.2021.126956
Keywords
Dielectric barrier discharge plasma; Microcystis aeruginosa; Microcystin-LR; Reactive oxygen species; Inactivation mechanism
Categories
Funding
- Shaanxi Natural Science Foundation (China) [2021JM-109]
- Overseas Student's Science and Technology Activities Project Merit Funding of Shaanxi
- Fundamental Research Funds for the Central Universities (China) [2452017106]
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This study successfully eliminated M. aeruginosa in water using a self-cooling dielectric barrier discharge plasma reactor, leading to loss of regenerative ability and mineralization of the treated cells. The toxin microcystin-LR initially increased during treatment but later decreased below 1 μg/mL.
Microcystis aeruginosa (M. aeruginosa), as the representative hazardous algae in cyanobacteria blooms, has long posed a threat to aquatic ecosystems. Here, a self-cooling dielectric barrier discharge plasma (DBDP) reactor was used to eliminate M. aeruginosa in water. The removal efficiency and mechanism of DBDP for M. aeruginosa and its toxin release during the treatment process was investigated. The results showed that over 99% of M. aeruginosa cells were removed by DBDP over 60 min under optimal conditions, and treated M. aeruginosa lost their ability to reproduce entirely. Reactive species generated in the self-cooling DBDP reactor damaged the membrane of M. aeruginosa, leading to leakage and degradation of dissolved organic matter. Increased intracellular reactive oxygen species accelerated the breakdown of protein and enzyme, and causes cell cytolysis. Eventually, M. aeruginosa was mineralized and lost its activity. The center dot OH, O-1(2) and center dot O-2(-) were crucial for inactivating M. aeruginosa. During the treatment process, the toxin microcystin-LR increased in the first 20 min, but declined over time: its concentration fell below 1 mu g.mL(-1) after 60 min. This study provides insight into M. aeruginosa' s elimination in water by DBDP and has significant implications for developing a plasma technique to curtail cyanobacteria bloom.
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