Oxidation to Control Cyanobacteria and Cyanotoxins in Drinking Water Treatment Plants: Challenges at the Laboratory and Full-Scale Plants

The impact of oxidation on mitigation of cyanobacteria and cyanotoxins in drinking water treatment sludge was investigated at the laboratory and treatment plant scales. Two common oxidants, KMnO<sub>4</sub> (5 and 10 mg/L) and H<sub>2</sub>O<sub>2</sub> (10 and 20...

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Main Authors: Farhad Jalili, Hana Trigui, Juan Francisco Guerra Maldonado, Sarah Dorner, Arash Zamyadi, B. Jesse Shapiro, Yves Terrat, Nathalie Fortin, Sébastien Sauvé, Michèle Prévost
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Water
Subjects:
Online Access:https://www.mdpi.com/2073-4441/14/4/537
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author Farhad Jalili
Hana Trigui
Juan Francisco Guerra Maldonado
Sarah Dorner
Arash Zamyadi
B. Jesse Shapiro
Yves Terrat
Nathalie Fortin
Sébastien Sauvé
Michèle Prévost
author_facet Farhad Jalili
Hana Trigui
Juan Francisco Guerra Maldonado
Sarah Dorner
Arash Zamyadi
B. Jesse Shapiro
Yves Terrat
Nathalie Fortin
Sébastien Sauvé
Michèle Prévost
author_sort Farhad Jalili
collection DOAJ
description The impact of oxidation on mitigation of cyanobacteria and cyanotoxins in drinking water treatment sludge was investigated at the laboratory and treatment plant scales. Two common oxidants, KMnO<sub>4</sub> (5 and 10 mg/L) and H<sub>2</sub>O<sub>2</sub> (10 and 20 mg/L) were applied under controlled steady-state conditions. Non-oxidized and oxidized sludge was left to stagnate in the dark for 7 to 38 days. Controlled laboratory trials show that KMnO<sub>4</sub> and H<sub>2</sub>O<sub>2</sub> decreased cell counts up to 62% and 77%, respectively. The maximum total MC level reduction achieved after oxidation was 41% and 98% using 20 mg/L H<sub>2</sub>O<sub>2</sub> and 10 mg/L KMnO<sub>4</sub>, respectively. Stagnation caused cell growth up to 2.6-fold in 8 out of 22 oxidized samples. Microcystin (MC) producer orders as Chroococcales and Synechococcales were persistent while Nostocales was sensitive to combined oxidation and stagnation stresses. In parallel, two on-site shock oxidation treatments were performed in the DWTP’s sludge holding tank using 10 mg/L KMnO<sub>4</sub>. On-site shock oxidation decreased taxonomic cell counts by up to 43% within 24 h. Stagnation preceded by on-site shock oxidation could increase total cell counts by up to 55% as compared to oxidation alone. The increase of cell counts and <i>mcyD</i> gene copy numbers during stagnation revealed the impact of oxidation/stagnation on cyanobacterial cell growth. These findings show the limitations of sludge oxidation as a strategy to manage cyanobacteria and cyanotoxins in sludge and suggest that alternative approaches to prevent the accumulation and mitigation of cyanobacteria in sludge should be considered.
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spelling doaj.art-cf91fdd315884806a4ec9cf64607914e2023-11-23T22:33:31ZengMDPI AGWater2073-44412022-02-0114453710.3390/w14040537Oxidation to Control Cyanobacteria and Cyanotoxins in Drinking Water Treatment Plants: Challenges at the Laboratory and Full-Scale PlantsFarhad Jalili0Hana Trigui1Juan Francisco Guerra Maldonado2Sarah Dorner3Arash Zamyadi4B. Jesse Shapiro5Yves Terrat6Nathalie Fortin7Sébastien Sauvé8Michèle Prévost9Department of Civil, Mineral and Mining Engineering, Polytechnique Montréal, Montréal, QC H3C 3A7, CanadaDepartment of Civil, Mineral and Mining Engineering, Polytechnique Montréal, Montréal, QC H3C 3A7, CanadaDepartment of Civil, Mineral and Mining Engineering, Polytechnique Montréal, Montréal, QC H3C 3A7, CanadaDepartment of Civil, Mineral and Mining Engineering, Polytechnique Montréal, Montréal, QC H3C 3A7, CanadaFaculty of Engineering and Information Technology, University of Melbourne, Melbourne, VIC 3010, AustraliaDepartment of Biological Sciences, University of Montréal, Montréal, QC H2V 0B3, CanadaDepartment of Biological Sciences, University of Montréal, Montréal, QC H2V 0B3, CanadaNational Research Council Canada, Energy, Mining and Environment, Montréal, QC H4P 2R2, CanadaDepartment of Chemistry, University of Montréal, Montréal, QC H3C 3J7, CanadaDepartment of Civil, Mineral and Mining Engineering, Polytechnique Montréal, Montréal, QC H3C 3A7, CanadaThe impact of oxidation on mitigation of cyanobacteria and cyanotoxins in drinking water treatment sludge was investigated at the laboratory and treatment plant scales. Two common oxidants, KMnO<sub>4</sub> (5 and 10 mg/L) and H<sub>2</sub>O<sub>2</sub> (10 and 20 mg/L) were applied under controlled steady-state conditions. Non-oxidized and oxidized sludge was left to stagnate in the dark for 7 to 38 days. Controlled laboratory trials show that KMnO<sub>4</sub> and H<sub>2</sub>O<sub>2</sub> decreased cell counts up to 62% and 77%, respectively. The maximum total MC level reduction achieved after oxidation was 41% and 98% using 20 mg/L H<sub>2</sub>O<sub>2</sub> and 10 mg/L KMnO<sub>4</sub>, respectively. Stagnation caused cell growth up to 2.6-fold in 8 out of 22 oxidized samples. Microcystin (MC) producer orders as Chroococcales and Synechococcales were persistent while Nostocales was sensitive to combined oxidation and stagnation stresses. In parallel, two on-site shock oxidation treatments were performed in the DWTP’s sludge holding tank using 10 mg/L KMnO<sub>4</sub>. On-site shock oxidation decreased taxonomic cell counts by up to 43% within 24 h. Stagnation preceded by on-site shock oxidation could increase total cell counts by up to 55% as compared to oxidation alone. The increase of cell counts and <i>mcyD</i> gene copy numbers during stagnation revealed the impact of oxidation/stagnation on cyanobacterial cell growth. These findings show the limitations of sludge oxidation as a strategy to manage cyanobacteria and cyanotoxins in sludge and suggest that alternative approaches to prevent the accumulation and mitigation of cyanobacteria in sludge should be considered.https://www.mdpi.com/2073-4441/14/4/537cyanobacteriashotgun metagenomic sequencingsludgedrinking water treatment plantoxidationstorage
spellingShingle Farhad Jalili
Hana Trigui
Juan Francisco Guerra Maldonado
Sarah Dorner
Arash Zamyadi
B. Jesse Shapiro
Yves Terrat
Nathalie Fortin
Sébastien Sauvé
Michèle Prévost
Oxidation to Control Cyanobacteria and Cyanotoxins in Drinking Water Treatment Plants: Challenges at the Laboratory and Full-Scale Plants
Water
cyanobacteria
shotgun metagenomic sequencing
sludge
drinking water treatment plant
oxidation
storage
title Oxidation to Control Cyanobacteria and Cyanotoxins in Drinking Water Treatment Plants: Challenges at the Laboratory and Full-Scale Plants
title_full Oxidation to Control Cyanobacteria and Cyanotoxins in Drinking Water Treatment Plants: Challenges at the Laboratory and Full-Scale Plants
title_fullStr Oxidation to Control Cyanobacteria and Cyanotoxins in Drinking Water Treatment Plants: Challenges at the Laboratory and Full-Scale Plants
title_full_unstemmed Oxidation to Control Cyanobacteria and Cyanotoxins in Drinking Water Treatment Plants: Challenges at the Laboratory and Full-Scale Plants
title_short Oxidation to Control Cyanobacteria and Cyanotoxins in Drinking Water Treatment Plants: Challenges at the Laboratory and Full-Scale Plants
title_sort oxidation to control cyanobacteria and cyanotoxins in drinking water treatment plants challenges at the laboratory and full scale plants
topic cyanobacteria
shotgun metagenomic sequencing
sludge
drinking water treatment plant
oxidation
storage
url https://www.mdpi.com/2073-4441/14/4/537
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