Evaluation of costs associated with atmospheric mercury emission reductions from coal combustion in China in 2010 and projections for 2020

2018 ◽  
Vol 610-611 ◽  
pp. 796-801 ◽  
Author(s):  
Yue Zhang ◽  
Xuejie Ye ◽  
Tianjun Yang ◽  
Jinling Li ◽  
Long Chen ◽  
...  
2020 ◽  
pp. 118175
Author(s):  
Xinyu Li ◽  
Zhonggen Li ◽  
Ji Chen ◽  
Leiming Zhang ◽  
Runsheng Yin ◽  
...  

2016 ◽  
Author(s):  
Hui Zhong ◽  
Yu Zhao ◽  
Marilena Muntean ◽  
Lei Zhang ◽  
Jie Zhang

Abstract. A better understanding of the discrepancies in multi-scale inventories could give an insight on their approaches and limitations, and provide indications for further improvements; international, national and plant-by-plant data sources are primarily obtained to compile those inventories. In this study we develop a high-resolution inventory of Hg emissions at 0.05° × 0.05° for Jiangsu China using a bottom-up approach and then compare the results with available global/national inventories. With detailed information on individual sources and the updated emission factors from field measurements incorporated, the annual Hg emissions of anthropogenic origin in Jiangsu 2010 are estimated at 39 105 kg, of which 51 %, 47 % and 2 % were released as Hg0, Hg2+, and HgP, respectively. This provincial inventory is thoroughly compared to the downscaled results from three national inventories (NJU, THU and BNU) and two global inventories (AMAP/UNEP and EDGARv4.tox2). Attributed to varied methods and data sources, clear information gaps exist in multi-scale inventories, leading to differences in the emission levels, speciation and spatial distributions of atmospheric Hg. The total emissions in the provincial inventory are the largest, i.e., 28 %, 7 %, 19 %, 22 %, and 70 % higher than NJU, THU, BNU, AMAP/UNEP, and EDGARv4.tox2, respectively. For major sectors including power generation, cement, iron & steel and other coal combustion, the Hg contents (HgC) in coals/raw materials, abatement rates of air pollution control devices (APCD) and activity levels are identified as the crucial parameters responsible for the differences in estimated emissions between inventories. Regarding speciated emissions, larger fraction of Hg2+ is found in the provincial inventory than national and global inventories, resulting mainly from the results by the most recent domestic studies in which enhanced Hg2+ were measured for cement and iron & steel plants. Inconsistent information of big power and industrial plants is the main source of differences in spatial distribution of emissions between the provincial and other inventories, particularly in southern and northwestern Jiangsu where intensive coal combustion and industry are located. Quantified with Monte-Carlo simulation, uncertainties of provincial Hg emissions are smaller than those of NJU national inventory, resulting mainly from the more accurate activity data of individual plants and the reduced uncertainties of HgC in coals/raw materials.


Resources ◽  
2020 ◽  
Vol 9 (11) ◽  
pp. 127
Author(s):  
Justyna Auguścik-Górajek ◽  
Marek Nieć

The mercury content in bituminous coal in Poland varies depending on the coal basin. The highest of its concentrations are recorded in the Lower Silesian Coal Basin where this may be the result of the volcanic activity reported there. A much lower average of Hg content was recorded in Lublin and the Upper Silesian Coal Basins (LCB and USCB), although it was higher in the former. A higher mercury concentration in the LCB is probably related to the zone of supposed deep disturbances, named the Karpinsky lineament. Most published works present the data on the mercury content in the bulk of mined coal. The preliminary assessment of mercury content in coal seams indicates that it varies considerably between and within them. It is bound to the presence of arsenic-bearing iron sulfides. Concentration of mercury in small zones of limited extent suggests it was introduced by migrating fluids. The knowledge of mercury content distribution in coal seams would improve the prediction of its content in the mined coal and allow better management of produced coal quality with the aim of reducing mercury emission to the atmosphere as a result of coal combustion.


2019 ◽  
Vol 33 (3) ◽  
pp. 1937-1943 ◽  
Author(s):  
Zikang Cui ◽  
Zhonggen Li ◽  
Yanzhe Zhang ◽  
Xuefeng Wang ◽  
Qili Li ◽  
...  

2016 ◽  
Vol 16 (23) ◽  
pp. 15119-15134 ◽  
Author(s):  
Hui Zhong ◽  
Yu Zhao ◽  
Marilena Muntean ◽  
Lei Zhang ◽  
Jie Zhang

Abstract. A better understanding of the discrepancies in multi-scale inventories could give an insight into their approaches and limitations as well as provide indications for further improvements; international, national, and plant-by-plant data are primarily obtained to compile those inventories. In this study we develop a high-resolution inventory of Hg emissions at 0.05°  ×  0.05° for Jiangsu, China, using a bottom-up approach and then compare the results with available global/national inventories. With detailed information on individual sources and the updated emission factors from field measurements applied, the annual Hg emissions of anthropogenic origin in Jiangsu in 2010 are estimated at 39 105 kg, of which 51, 47, and 2 % were Hg0, Hg2+, and Hgp, respectively. This provincial inventory is thoroughly compared to three downscaled national inventories (NJU, THU, and BNU) and two global ones (AMAP/UNEP and EDGARv4.tox2). Attributed to varied methods and data sources, clear information gaps exist in multi-scale inventories, leading to differences in the emission levels, speciation, and spatial distributions of atmospheric Hg. The total emissions in the provincial inventory are 28, 7, 19, 22, and 70 % larger than NJU, THU, BNU, AMAP/UNEP, and EDGARv4.tox2, respectively. For major sectors, including power generation, cement, iron and steel, and other coal combustion, the Hg contents (HgC) in coals/raw materials, abatement rates of air pollution control devices (APCDs) and activity levels are identified as the crucial parameters responsible for the differences in estimated emissions between inventories. Regarding speciated emissions, a larger fraction of Hg2+ is found in the provincial inventory than national and global inventories, resulting mainly from the results by the most recent domestic studies in which enhanced Hg2+ were measured for cement and iron and steel plants. Inconsistent information on large power and industrial plants is the main source of differences in spatial distribution of emissions between the provincial and other inventories, particularly in southern and northwestern Jiangsu, where intensive coal combustion and industry are located. Quantified with Monte Carlo simulation, uncertainties in the provincial inventory are smaller than those of the NJU national inventory, resulting mainly from the more accurate activity data of individual plants and the reduced uncertainties in HgC in coals/raw materials.


2018 ◽  
Author(s):  
Basil Denzler ◽  
Christian Bogdal ◽  
Cyrill Kern ◽  
Anna Tobler ◽  
Jing Huo ◽  
...  

Abstract. Mercury is a heavy metal of particular concern due to its adverse effects on the human health and the environment. Recognizing this problem, the UN Minamata Convention on Mercury was recently adopted, where signatory countries agreed to reduce anthropogenic mercury emissions. To evaluate the effectiveness of the convention, quantitative knowledge on mercury emissions is crucial. So far, bottom-up approaches have successfully been applied to quantify mercury emission – especially for point sources. Distributed sources make up for a large share of the emission, however, they are still poorly characterized. Here, we present a top-down approach to estimate mercury emissions based on atmospheric measurements in the city of Zurich, Switzerland. While monitoring the atmospheric mercury concentrations during inversion periods in Zurich, we were able to relate the concentration increase to the mercury emission strength of the city using a box model. By the means of this boundary-layer budget approach, we succeeded to narrow down the emissions of Zurich to range between 41 ± 8 kg/a (upper bound) and 24 ± 8 kg/a (lower bound). Thereby, we could quantify emissions from mixed, diffuse and point like sources and derive an annual mercury per capita emission of 0.06 to 0.10 g/a. The approach presented here has the potential to support authorities in setting up inventories and to validate emission estimations derived from the commonly applied bottom-up approaches. Furthermore, our method is applicable to other compounds and to a wide range of cities or other areas, where sources or as well sinks for mercury and other atmospheric pollutants are presumed.


2015 ◽  
Vol 33 ◽  
pp. 125-134 ◽  
Author(s):  
Maria Pia Ancora ◽  
Lei Zhang ◽  
Shuxiao Wang ◽  
Jeremy Schreifels ◽  
Jiming Hao

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