Microcystins (MCs) are toxins produced by cyanobacteria commonly found in harmful algal blooms (HAB) occurring in many surface waters. Conventional methods for removing MC-LR such as membrane filtration and activated carbon are only phase change removal methods and are often expensive in operation and maintenance. It is urgent to develop a rapid, easy-to-use, and cost-effective method for the degradation of MC-LR. In this study, a novel Au-decorated Ni-metal-organic framework (Au/Ni-MOF) was newly developed on a hydrophilic carbon fiber paper (2 cm × 2 cm) using an air spraying method. The Au/Ni-MOF was then applied for the photodegradation of MC-LR in water under UV-Vis. The addition of Au onto the surface of the Ni-MOF resulted in a nearly fivefold enhancement in the reaction rate coefficient (k), reaching a value of 0.0599 min for the photodegradation of MC-LR (initial concentration of 20 ppb). It was found that 94.2% of MC-LR removal was attributed to photodegradation, with the remaining 5.8% from adsorption. The rate coefficient of 20 ppb of MC-LR in the surface water sample (pH 6.0) was 0.06 min likely due to the presence of other contaminates including scavenger agents within the sample which inhibits the degradation reaction of the MC-LR. Overall, this study demonstrated the potential for the novel Au/Ni-MOF to effectively reduce the concentration of the MC-LR toxin in the contaminated water.
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http://dx.doi.org/10.1016/j.chemosphere.2023.140404 | DOI Listing |
Chemosphere
September 2024
Key Laboratory of Jiangxi Province for Persistent Pollutants Prevention Control and Resource Reuse, Nanchang Hangkong University, Nanchang, 330063, PR China; National-Local Joint Engineering Research Center of Heavy Metals Pollutants Control and Resources Utilization, Nanchang Hangkong University, Nanchang, 330063, PR China; School of Life Science, Jinggangshan University, Ji'an, 343009, PR China.
Photocatalytic degradation of pollutants coupled with hydrogen (H) evolution has emerged as a promising solution for environmental and energy crises. However, the fast recombination of photoexcited electrons and holes limits photocatalytic activities. Herein, an S-scheme heterojunction carbon doped-TiO/ZnInS (C-TiO/ZnInS) was designed by substituting oxygen sites within C-TiO by ZnInS.
View Article and Find Full Text PDFEnviron Res
July 2024
School of Materials Science and Engineering, Peking University, Beijing, 100871, China.
Photocatalysis was an attractive strategy that had potential to tackle the Microcystin-LR (MC-LR) contamination of aquatic ecosystems. Herein, magnetic photocatalyst FeO/BiWO/Reduced graphene oxide composites (BiWO/FeO/RGO) were employed to degrade MC-LR. The removal efficiency and kinetic constant of the optimized BiWO/FeO/RGO (BiWO/FeO-40%/RGO) was 1.
View Article and Find Full Text PDFChemosphere
December 2023
Department of Civil, Environmental, and Construction Engineering, University of Central Florida, Orlando, FL, 32816, United States. Electronic address:
Microcystins (MCs) are toxins produced by cyanobacteria commonly found in harmful algal blooms (HAB) occurring in many surface waters. Conventional methods for removing MC-LR such as membrane filtration and activated carbon are only phase change removal methods and are often expensive in operation and maintenance. It is urgent to develop a rapid, easy-to-use, and cost-effective method for the degradation of MC-LR.
View Article and Find Full Text PDFJ Environ Sci (China)
January 2024
Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095, China.
Inactivation of cyanobacterial cells and simultaneous control of secondary metabolites is of significant necessity for the treatment of cyanobacteria-laden water. Acetylacetone (AcAc) has been reported a specific algicide to inactivate Microcystis aeruginosa (M. aeruginosa) and an effective light activator to degrade pollutants.
View Article and Find Full Text PDFWater Res
September 2023
Department of Environmental Science & Engineering, Fudan University, Shanghai 200433, PR China. Electronic address:
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