The lifetime of elemental mercury in the marine boundary layer(MBL) has been studied using AMCOTS (Atmospheric Mercury Chemistry Over The Sea), a box model of MBL photochemistry including aerosols and detailed mercury chemistry. Recently measured Hg(0)(g) oxidation reactions have been included, and the studies were performed as a function of latitude, time of year, boundary layer liquid water content (LWC) and cloud optical depth. The results show that Hg has the shortest lifetime when air temperatures are low and sunlight and deliquescent aerosol particles are plentiful. Thus the modeled lifetime for clear-sky conditions is actually shorter at mid-latitudes and high latitudes than near the equator, and for a given latitude and time of year, cooler temperatures enhance the rate of Hg oxidation. Under typical summer conditions (for a given latitude) of temperature and cloudiness, the lifetime (tau) of Hg(0)(g) in the MBL is calculated to be around 10 days at all latitudes between the equator and 60 degrees N. This is much shorter than the generally accepted atmospheric residence time for Hg(0)(g) of a year or more. Given the relatively stable background concentrations of Hg(0)(g) which have been measured, continual replenishment of Hg(0)(g) must take place, suggesting a "multihop" mechanism for the distribution of Hg, rather than solely aeolian transport with little or no chemical transformation between source and receptor. Inclusion of an empirical Hg(0)(g) emission factor related to insolation was used to stabilize the Hg(0)(g) concentration in the model, and the emission rates necessarily agree well with estimated emission fluxes for the open ocean.
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http://dx.doi.org/10.1021/es034623z | DOI Listing |
Water Res
October 2024
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; College of Resources and Environment, University of Chinese Academy of Sciences, Beijing 100049, China; School of Environment, Hangzhou Institute for Advanced Study, UCAS, Hangzhou 310024, China.
Mercury (Hg) emissions from Hg smelting (roasting HgS ores) and artisanal small-scale gold mining predominantly include elemental Hg, in either liquid [Hg(0)] or gaseous [Hg(0)] form. The oxidation of Hg(0) into Hg(I) is the first step during Hg(0) oxidation, which enables Hg to enter the food web. However, this oxidation process remains poorly understood, particularly in Hg(0)/Hg(0)-impacted environments.
View Article and Find Full Text PDFJ Hazard Mater
March 2023
Environmental Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, United States; Department of Biosystems Engineering and Soil Science, University of Tennessee, Knoxville, TN 37996, United States. Electronic address:
Over 3000 mercury (Hg)-contaminated sites worldwide contain liquid metallic Hg [Hg(0)] representing a continuous source of elemental Hg(0) in the environment through volatilization and solubilization in water. Currently, there are few effective treatment technologies available to remove or sequester Hg(0) in situ. We investigated sonochemical treatments coupled with complexing agents, polysulfide and sulfide, in oxidizing Hg(0) and stabilizing Hg in water, soil and quartz sand.
View Article and Find Full Text PDFJ Phys Chem A
October 2022
Department of Chemistry, McGill University, 801 Sherbrooke West, Montreal, QC H3A 2K6, Canada.
Mineral dust aerosols play an important role in tropospheric chemistry and aerosol-cloud interaction processes. Yet, their interactions with gaseous elemental mercury (Hg) are not currently well understood. Using a coated-wall flow tube (CWFT) reactor, we measured the uptake of Hg on some common components of mineral dust aerosols, including TiO, AlO, and FeO, and the effects of irradiation (dark, visible and UV-A) and relative humidity (<2% to 60%) on the uptake kinetics.
View Article and Find Full Text PDFEnviron Pollut
January 2021
Institute of Surface-Earth System Science, School of Earth System Science, Tianjin University, Tianjin, 300072, China.
The installation rate of denitrification devices is accelerating in Chinese urban boilers. Previous studies on pulverized coal-fired boilers without denitrification devices showed that combustion products containing mainly oxidized mercury (Hg) preferably enriched lighter Hg isotopes than feed coals. However, the magnitude of this enrichment becomes less pronounced if denitrification devices are installed.
View Article and Find Full Text PDFEnviron Sci Technol
July 2019
State Key Laboratory of Coal Combustion, School of Energy and Power Engineering , Huazhong University of Science and Technology, 1037 Luoyu Road , Wuhan , 430074 , PR China.
Mercury emission is an important issue during in-situ gasification chemical-looping combustion ( iG-CLC) of coal. This work focused on experimentally "isolating" two elementary subprocesses (coal pyrolysis and char gasification) during iG-CLC of coal, identifying mercury distribution within the two subprocesses, and examining the effects of a hematite oxygen carrier (OC) on the mercury fate. The mercury measurement accuracy was carefully ensured by comparing online measurements (by a VM 3000 instrument) and benchmark measurements (by the standard Ontario Hydro Method, ASTM D6784) as well as repeated tests (10 times for each case).
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