4.8 Article

Coremoval of Energetics and Oxyanions via the In Situ Coupling of Catalytic and Enzymatic Destructions: A Solution to Ammunition Wastewater Treatment

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 57, 期 1, 页码 666-673

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c05675

关键词

RDX; nitrate and perchlorate; Pd catalysis; microbial mineralization; continuous flow reactor

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This paper presents a low-energy strategy for treating ammunition wastewater, involving catalytic denitration and microbial mineralization combined with oxyanion reduction. The results show that RDX can be rapidly denitrated in the presence of a suitable catalyst, while nitrate and perchlorate can be efficiently biodegraded.
Ammunition wastewater contains toxic nitrated explosives like RDX and oxyanions like nitrate and perchlorate. Its treatment is challenged by low efficiency due to contaminant recalcitrance and high cost due to multiple processes needed for separately removing different contaminant types. This paper reports a H-2-based low-energy strategy featuring the treatment of explosives via catalytic denitration followed by microbial mineralization coupled with oxyanion reduction. After a nitrate- and perchlorate-reducing biofilm incapable of RDX biodegradation was coated with palladium nanoparticles (Pd(0)NPs), RDX was rapidly denitrated with a specific catalytic activity of 8.7 g(cat)(-1) min(-1), while biological reductions of nitrate and perchlorate remained efficient. In the subsequent 30-day continuous test, >99% of RDX, nitrate, and perchlorate were coremoved, and their effluent concentrations were below their respective regulation levels. Detected intermediates and shallow metagenome analysis suggest that the intermediates after Pd-catalytic denitration of RDX ultimately were enzymatically utilized by the nitrate- and perchlorate-reducing bacteria as additional electron donor sources.

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