Solving the puzzle of mercury fate and emissions by coal-fired power plants: The potential of hydrodynamic-atmospheric modelling.

There is currently a significant gap in knowledge about the emission and deposition of mercury (Hg) from coal-fired power plants in Australia. To fill this gap, we propose a novel method that combines several sources of information (stratigraphic data, hydrodynamic modelling and atmospheric modelling), to identify the sources and fates of Hg emitted from coal-fired power plants. The stratigraphic record from Lake Macquarie (Australia) shows that mercury deposition increased up to 7-times since the 1950s, which is when coal-fired power plants were commissioned in the catchment. The stratigraphy also shows a decrease in Hg deposition with power plant retrofits. Using results from multiple models (statistical modelling, hydrodynamic modelling, particle density modelling and atmospheric emissions modelling), we found that ash dams contribute little Hg to Lake Macquarie. Instead, most of the Hg contamination in the lake is a result of atmospheric emissions from the power plants, and these power plants are also depositing Hg in the urban areas to the west of the lake. Our results demonstrate that the multi-proxy approach demonstrated in the paper can be used to provide clues as to the source of Hg, so that appropriate mitigation strategies and regulatory frameworks can be implemented.

A Pilot Survey of Potentially Hazardous Trace Elements in the Aquatic Environment Near a Coastal Coal-Fired Power Plant in Taiwan.

BACKGROUND: A limited number of potentially hazardous trace elements were quantified in the aquatic environment near the world's second largest coal-fired power plant (CFPP) and the coal combustion residual (CCR) disposition sites in Central Taiwan. We postulated that contamination from specific trace elements would be present in the abovementioned aquatic environments. METHODS: Cross-sectional sampling of trace elements was first performed between September 24, 2017 and October 3, 2017 outside the CFPP, in the effluent sampled from Changhua, a county south of metropolitan Taichung, and at the historical CCR disposal sites, using the intertidal zone surface seawater and the seawater in an oyster farm as controls. Aqueous samples were collected from 12 locations for analysis of 13 trace elements (Al, As, B, Cd, total Cr, Co, Fe, Pb, Mn, Se, Sr, Tl, and V). We used inductively coupled plasma (ICP) optical emission spectrometry to determine B and Fe levels, and ICP mass spectrometry for all other trace elements. The Spearman rank correlation coefficient (Rho) was calculated to examine the pairwise relation among the trace elements. RESULTS: Al (50% of all samples), B (66.7%), Fe (25%), Mn (50%), Sr (8.3%), and V (25%) were identified as being above the Environmental Protection Agency (EPA) regulation limit. The oyster farm seawater had no concerns. Mn (96.4 µg/L) in the CFPP drainage effluent was 1.9-fold above the regulation limit. Fe, Mn, and V were detected from the cooling channel at 4379, 625, and 11.3 µg/L, respectively. The effluent and water from the areas surrounding the 2 CCR dump sites revealed similar magnitudes of trace element contamination. B is highly correlated with Sr (Rho = 0.94, 95% confidence interval [CI], 0.80-0.98). Meanwhile, Fe is highly correlated with Al (Rho = 0.77), Pb (Rho = 0.71), Co (Rho = 0.75), and V (Rho = 0.84). CONCLUSIONS: The EPA must set an explicit regulation limit for aluminum, boron, iron, and strontium in the aquatic environment. This exploratory research will inform policymaking regarding certain trace elements that could potentially have an adverse impact on public health and wildlife.