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Updated: Mar 21, 2026

Implementation of a Hyperbolic Vortex Plasma Reactor for the Removal of Micropollutants in Water
Published on: July 25, 2025
Enhanced pollutant removal in multi-pollutants contaminated water by bioaugmented slow filtration
Tingming Ye1, Peng Li2, Zilong Zhou2
1Key Laboratory of Environmental Aquatic Chemistry, State Key Laboratory of Regional Environment and Sustainability, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; Jibei Electric Power Research Institute, State Grid Jibei Electric Power Co., Ltd., Beijing 100045, China.
Abstract:
Slow filtration is a low-cost and low-carbon water treatment approach, yet its broad application is limited by long start-up times and insufficient understanding of multi-pollutant removal. Here, we evaluate whether bioaugmentation with manganese-oxidizing bacteria enhances pollutant removal in water contaminated with NH4+ -N, Mn2+, readily biodegradable emerging contaminants (ECs, atenolol and trimethoprim), and relatively non-biodegradable ECs (carbamazepine and sulfamethoxazole). Bioaugmented filtration increased the removal rates of NH4+-N and Mn2+ by 32.2% and 33.9%, respectively, during the first 10 days of the experiment. The proposed approach also demonstrated superior average removal rates (30.1%-99.6%) of four ECs compared to the filter column without QJX-1 inoculation (16.7%-99.3%). Furthermore, bioaugmented filtration effectively reduced the relative abundances of antibiotic resistance genes (ARGs) subtypes such as macB, tetA(58), and bcrA in the influent. The composition of ARGs on the filter media in both process groups is highly similar, with the relative abundance of ARGs at the top and middle of the filter column slightly higher than at the bottom. The mechanism study revealed that Mn2+ was effectively oxidized to biological manganese oxides, which was conducive to the adsorption and oxidation of Mn2+ and ECs. The metagenomic results confirmed the pmoC-amoC gene in Nitrospira promoted the removal of NH4+-N. Toxicity prediction indicated that the toxicity of most ECs intermediates was significantly lower than that of their parent compounds. The findings of this study verify the viability of employing cost-effective and few-chemical water treatment technologies to treat muti-pollutant contaminated water and guarantee the quality of drinking water.
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