Mobility of trace elements in black shale assessed by leaching tests and sequential chemical extraction

2009 ◽  
Vol 9 (1) ◽  
pp. 71-79 ◽  
Author(s):  
Ulf Lavergren ◽  
Mats E. Åström ◽  
Bo Bergbäck ◽  
Henning Holmström
2018 ◽  
Vol 36 (6) ◽  
pp. 1655-1673
Author(s):  
Shenjun Qin ◽  
Qingfeng Lu ◽  
Kang Gao ◽  
Penghui Bo ◽  
Shihao Wu

The enrichment and geochemical significance of elements associated with Late Permian coals in Southwest China have always gained widespread interest in the field of coal geology. The present study focuses on the geochemical characterization of Late Permian coal in the Zhongliangshan mine. Twenty-three samples were collected from the K1a coal seam of the Zhongliangshan mine, and the major and trace elements in the coal were analyzed by using X-ray fluorescence spectroscopy (XRF) and inductively coupled plasma mass spectrometry. The composition of minerals in the Zhongliangshan coal, and the modes of occurrence of coal-associated elements, especially those with elevated contents, were studied through a combination of microscopic analyses, X-ray powder diffraction, and scanning electron microscope – energy dispersive X-ray spectrometer. The minerals in coal mainly consist of kaolinite, pyrite, calcite, and quartz, as well as small amount of gypsum and anatase. Compared with the average elemental concentrations in world coal, the Zhongliangshan coal is enriched in Cr, and slightly enriched in Li, U, Sr, V and Ag. Combining the correlation analysis and sequential chemical extraction experiments, it can be inferred that many trace elements in the Zhongliangshan coal have both inorganic and organic affinities. The elements Cr, Li, and V mainly occur in clay minerals, and also are related to organic matter in the coal. Uranium presents firstly in the organic and then silicate states. Strontium shows multiple modes of occurrence including carbonate, silicate, and exchangeable ion states, and Ag primarily occurs in sulfides followed by silicates. The terrigenous debris input from the Emeishan basalt is the major reason for the enrichment of above elements in the Zhongliangshan coal.


2011 ◽  
Vol 2011 ◽  
pp. 1-20 ◽  
Author(s):  
R. Burt ◽  
T. Weber ◽  
S. Park ◽  
S. Yochum ◽  
R. Ferguson

Long-term mining activities in the mountains around Creede, Colorado have resulted in significant contamination in soils and water in the Willow Creek floodplain. Total major and trace were determined for soils and water and sequential chemical extraction for soils. Objectives were to determine concentrations and potential reactivity of trace elements and investigate their relationship with other soil and water properties. Water trace elements showed significant variability among sites, ranging from 347 to 12108 μg/L. Relative trend showed (Zn > Sr > Ba) > (Mn > W > Cd) > (Sn > V≈Ni≈Cu > Co) > (Ag). Soil trace elements showed significant short-range spatial variability, ranging from 2819 to 19274 mg/kg. Relative trend showed (Pb≈Zn > Mn > Ba > P) > (As > Cu > Sr > V > Cd > Sb≈Ag) > (Co≈Cr > Mo≈Sn≈Ni) > (Be≈W > Se≈Hg). Predominant fractions were oxide, specifically-sorbed/carbonate bound, and residual. Water soluble and exchangeable fractions showed (Zn≈Cd) > Pb and Cd > Zn > Pb, respectively. Mobility factors for highly contaminated soils showed Cd≈Zn > Pb > Cu > As.


Energies ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2361
Author(s):  
Yinjiao Su ◽  
Xuan Liu ◽  
Yang Teng ◽  
Kai Zhang

Coal combustion is an anthropogenic source of mercury (Hg) emissions to the atmosphere. The strong toxicity and bioaccumulation potential have prompted attention to the control of mercury emissions. Pyrolysis has been regarded as an efficient Hg removal technology before coal combustion and other utilization processes. In this work, the Hg speciation in coal and its thermal stability were investigated by combined sequential chemical extraction and temperature programmed decomposition methods; the effect of coal rank on Hg speciation distribution and Hg release characteristics were clarified based on the weight loss of coal; the amount of Hg released; and the emission of sulfur-containing gases during coal pyrolysis. Five species of mercury were determined in this study: exchangeable Hg (F1), carbonate + sulfate + oxide bound Hg (F2), silicate + aluminosilicate bound Hg (F3), sulfide bound Hg (F4), and residual Hg (F5), which are quite distinct in different rank coals. Generally, Hg enriched in carbonates, sulfates, and oxides might migrate to sulfides with the transformation of minerals during the coalification process. The order of thermal stability of different Hg speciation in coal is F1 < F5 < F2 < F4 < F3. Meanwhile, the release of Hg is accompanied with sulfur gases during coal pyrolysis, which is heavily dependent on the coal rank.


Molecules ◽  
2021 ◽  
Vol 26 (9) ◽  
pp. 2651
Author(s):  
Magdalena Jabłońska-Czapla ◽  
Katarzyna Grygoyć

The optimization and validation of a methodology for determining and extracting inorganic ionic Te(VI) and Te(IV) forms in easily-leached fractions of soil by Ion Chromatography-Inductively Coupled Plasma-Mass Spectrometry (IC-ICP-MS) were studied. In this paper, the total concentration of Te, pH, and red-ox potential were determined. Ions were successfully separated in 4 min on a Hamilton PRPX100 column with 0.002 mg/kg and 0.004 mg/kg limits of detection for Te(VI) and Te(IV), respectively. Soil samples were collected from areas subjected to the influence of an electrowaste processing and sorting plant. Sequential chemical extraction of soils showed that tellurium was bound mainly with sulphides, organic matter, and silicates. Optimization of soil extraction allowed 20% average extraction efficiency to be obtained, using 100 mM citric acid as the extractant. In the tested soil samples, both tellurium species were present. In most cases, the soils contained a reduced Te form, or the concentrations of both species were similar.


Energies ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 3119
Author(s):  
Yinjiao Su ◽  
Xuan Liu ◽  
Yang Teng ◽  
Kai Zhang

Mercury (Hg) is a toxic trace element emitted from coal conversion and utilization. Samples with different coal ranks and gangue from Ningwu Coalfield are selected and investigated in this study. For understanding dependence of mercury distribution characteristics on coalification degree, Pearson regression analysis coupled with Spearman rank correlation is employed to explore the relationship between mercury and sulfur, mercury and ash in coal, and sequential chemical extraction method is adopted to recognize the Hg speciation in the samples of coal and gangue. The measured results show that Hg is positively related to total sulfur content in coal and the affinity of Hg to different sulfur forms varies with the coalification degree. Organic sulfur has the biggest impact on Hg in peat, which becomes weak with increasing the coalification degree from lignite to bituminous coal. Sulfate sulfur is only related to Hg in peat or lignite as little content in coal. However, the Pearson linear correlation coefficients of Hg and pyritic sulfur are relatively high with 0.479 for lignite, 0.709 for sub-bituminous coal and 0.887 for bituminous coal. Hg is also related to ash content in coal, whose Pearson linear correlation coefficients are 0.504, 0.774 and 0.827 respectively, in lignite, sub-bituminous coal and bituminous coal. Furthermore, Hg distribution is directly depended on own speciation in coal. The total proportion of F2 + F3 + F4 is increased from 41.5% in peat to 87.4% in bituminous coal, but the average proportion of F5 is decreased from 56.8% in peat to 12.4% in bituminous coal. The above findings imply that both Hg and sulfur enrich in coal largely due to the migration from organic state to inorganic state with the increase of coalification degree in Ningwu Coalfield.


1974 ◽  
Vol 22 (2) ◽  
pp. 88-103 ◽  
Author(s):  
MARSHALL R. URIST ◽  
HISASHI IWATA ◽  
STUART D. BOYD ◽  
PETER L. CECCOTTI ◽  
MARLYS OKADA ◽  
...  

Data on physicochemical conditions leading to loss of the bone morphogenetic property of bone matrix in neutral buffer solutions support the concept of an enzymic control mechanism better than a chemical blocking reaction or denaturation. The loss is associated with release of 35S-labeled constituents and not prevented by ε-amino caproic acid, an inhibitor of cathepsins. The loss is also associated with release of 35S-cysteine-labeled protein; about 60% of the yield is sustained by the addition of only 3 mmoles/liter of iodoacetic acid. A latent period of about 12 hr, decreased by extraction of bone matrix with CaCl2, is characterized by release of protein polysaccharide and other noncollagenous proteins. Release of sialic acid from the bone matrix by neuraminidase at pH 7.4 has no effect upon bone yield. At 2°C, Tris-HCl buffer or ethylenediaminetetraacetic acid extracts noncollagenous proteins without loss of bone yield; at 37°C, pH 7.4, these solutions also activate endogenous enzymes and reduce bone yield. The component of bone matrix responsible for reduction in bone yield is separable from bone matrix by extraction with phosphate buffer, by catheptic digestion of bone matrix in acidic buffer solutions, by sequential chemical extraction of noncollagenous proteins with cold slightly acidic salt solutions or by extraction-denaturation with chloroform-methanol. Detergents neither extinguish nor denature the morphogenetic property but some solubilize or extract degradative enzymes; hexodecyl trimethyl ammonium bromide, at pH 5.0, is positively charged and extracts hydrophobic proteins, including part of the bone morphogenetic property. A special selection of sulfhydryl chemical inhibitors remarkably different from the selection inhibiting known enzymes preserves the bone morphogenetic property of bone matrix; p-chloromercuribenzoate preservation is reversible by chemical reactions with cysteine. Reduction in bone yield in phosphate buffer is not attributable to a chemical block because chloroform-methanol extraction of the agent does not restore bone yield and is not attributable to denaturation because bone yield sustained by p-chloromercuribenzoate is lost by chemical reactions with cysteine. An hypothetical insoluble bone morphogenetic protein (BMP) firmly bound to collagen is degraded by a soluble neutral proteinase (BMPase). Digestion of the hypothetical BMP occurs without loss of the 640-A electron micrographic image of bone collagen, resembles tryptic digestion and is more selective as well as physiologic in action.


Fuel ◽  
2019 ◽  
Vol 237 ◽  
pp. 555-565 ◽  
Author(s):  
Jinhe Pan ◽  
Changchun Zhou ◽  
Mengcheng Tang ◽  
Shanshan Cao ◽  
Cheng Liu ◽  
...  

2017 ◽  
Vol 35 (3) ◽  
pp. 376-387 ◽  
Author(s):  
Cunliang Zhao ◽  
Bangjun Liu ◽  
Jialiang Ma ◽  
Shiming Liu ◽  
Maksim G Blokhin

The occurrence of Rb and Cs in coal samples from Iqe coalfield was analyzed by a sequential chemical extraction experiment. Five types of Rb and Cs were determined in the coal: water soluble, ion exchangeable, organic bonded, carbonate, and silicate. The results indicated that the occurrence of Cs is similar with Rb in coal, and nearly all Rb and Cs are distributed in silicate. The occurrence of Rb and Cs is most likely associated with silicate minerals in coal. With the high correlation between Rb, Cs, and K, and the high content of kaolinite and illite in these coal samples, it can be inferred that illite probably is the main carrier of Rb and Cs. Minor amounts of Rb and Cs may also be adsorbed by kaolinite in Iqe coal, and Cs may exist in other states, such as an exchangeable ion.


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