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Unlabelled: Selective catalytic reduction (SCR) catalysts are deactivated by several mineral and metallic trace elements at highly variable rates determined by fuel quality and furnace firing conditions. With a loss in activity, NO is reduced over a longer inlet length of the SCR monolith, which leaves a shorter trailing section to sustain the most favorable conditions to oxidize Hg(0) and SO2. Since virtually no operating SCR was designed for Hg oxidation and since different monoliths are routinely combined as layers in particular units, the Hg oxidation performance of any SCR fleet is largely unmanaged. The analysis in this paper directly relates a measurement or manufacturer's forecast on the deterioration in NO reduction with age to corresponding estimates for oxidation of Hg(0). It accommodates any number of catalyst layers with grossly different properties, including materials from different manufacturers and different ages. In this paper, the analysis is applied to 16 full-scale SCRs in the Southern Company fleet to demonstrate that catalyst deactivation disrupts even the most prominent connections among the Hg(0) oxidation performance of commercial SCRs and the behavior of fresh catalysts at lab, pilot, and even full scale.
Implications: Catalyst deactivation confounds even the most prominent connections among the Hg(0) oxidation performance of commercial SCRs and the behavior of fresh catalyst at lab, pilot, and even full scale. The halogen dependence has been emphasized throughout the literature on catalytic Hg(0) oxidation, based on a large database on fresh catalysts. But for deactivated catalysts in commercial SCRs, the number of layers is much more indicative of the Hg(0) oxidation performance, in that SCRs with four layers perform better than those with three layers, and so on. The new qualified conclusion is that Hg(0) oxidation is greater for progressively greater HCl concentrations only among SCRs with the same number of layers, even for an assortment of catalyst design specifications and operating conditions.
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http://dx.doi.org/10.1080/10962247.2015.1107658 | DOI Listing |
J Hazard Mater
September 2025
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; School of Environment, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou 310024, China; Scho
Although methanogenic archaea are among the oldest microorganisms capable of mercury methylation, their contribution to methylmercury (MeHg) production has only recently gained attention. Studies with laboratory-cultivated methanogens elucidate the transformation of inorganic mercury (Hg) into MeHg, thereby uncovering underlying microbial methylation mechanisms. However, this field faces challenges such as significant Hg loss and unstable culture systems, which impede accurate assessment of these processes.
View Article and Find Full Text PDFMikrochim Acta
August 2025
Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Ubon Ratchathani University, Ubon Ratchathani, 34190, Thailand.
Two selective methods were developed for detecting mercury ions (Hg⁺) in food and water samples using catalytic fluorometry based on Au-Hg amalgamation with enhanced peroxidase-like activity. These approaches include (i) a laser-printed microfluidic paper-based analytical device (LP-µPAD) and (ii) a paper-based microcentrifuge tube test kit. The LP-µPAD was fabricated via commercial laser printing and integrated gold nanoparticles (AuNPs) with o-phenylenediamine (OPD) and hydrogen peroxide (H₂O₂).
View Article and Find Full Text PDFWater Res
July 2025
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Natural organic matter (NOM)-mediated non-photochemical oxidation of elemental mercury (Hg(0)), as an important process controlling Hg cycle, is still not well understood, particularly with respect to its electron transfer and environmental significance relevant to Hg(0) uptake by seawater. Here, we studied the uptake of atmospheric Hg(0) and its subsequent aqueous non-photochemical oxidation in seawater in the presence of NOM, by using extracellular polymeric substances and thiol compounds as NOM models. We observed NOM enhanced Hg(0) partition into seawater and its aqueous oxidation.
View Article and Find Full Text PDFEnviron Sci Technol
July 2025
Key Laboratory of Coal Science and Technology, Ministry of Education, College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, P. R. China.
Capturing mercury (Hg) in raw natural gas is crucial for the stable operation of natural gas purification systems. However, achieving direct oxidation removal of Hg in a reducing atmosphere at ambient temperature presents a significant challenge. In this study, we designed a Cu-doped OMS-2 sorbent, synthesized with citric acid (CA) assistance, which demonstrated exceptional Hg removal performance in simulated natural gas at ambient temperature.
View Article and Find Full Text PDFJ Hazard Mater
September 2025
Center of Molecular Ecophysiology (CMEP), College of Resources and Environment, Southwest University, Chongqing 400715, China; Yibin Academy of Southwest University, Yibin, Sichuan 644005, China. Electronic address:
Gaseous elemental mercury [Hg(0)] contamination has emerged as a critical global environmental threat owing to its persistent atmospheric mobility. Despite its ecological risks, the metabolic adaptation mechanisms of plants to Hg(0) stress remain largely unexplored. Here, we investigated the physiological and metabolic responses of Tillandsia usneoide, a bioindicator for atmospheric Hg(0), to Hg(0) exposure (∼300 μg m⁻³, an extreme concentration near point sources like Hg smelting, mining, and coal processing).
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