Geochemical and statistical analysis of trace metals in atmospheric particulates in Wuhan, central China

The geochemical characteristics of trace metals (As, Cr, Co, Cd, Cu, Mn, Ni, Pb, V and Zn) in PM10 in Wuhan, the biggest metropolitan in central China, as well as their sources and contributions were analyzed. As PM10 has been the principal contaminant of air in Wuhan for years, concentrations of trace metals were measured in PM10 using high-volume samplers at one urban (Hankou) and one industrial (Changqian) site in Wuhan between September 2003 and September 2004. Based on the results, PM10 in Wuhan is characterized by relatively high levels of As, Cd, Mn, Pb and Zn compared with other Asian cities. The time-series of these elements indicated that As, Cu and Zn at both sites have similar trends, whereas Pb levels showed different patterns due to different emission sources. Factor analysis was applied to the datasets focusing on the apportionment of the mass of selected trace metals. Results indicate that Pb, Cd and As have a common source (smelting) at both sites, whereas the sources of Ni vary from coal combustion and steel in Changqian to mineral and traffic in Hankou.     

Determination of elemental affinities by density fractionation of bulk coal samples from the Chongqing coal district, Southwestern China

The occurrence and distribution of major and trace elements have been investigated in two coal-bearing units in the Chonqing mining district (South China): the Late Permian and Late Triassic coals.The Late Permian coals have higher S contents than the Late Triassic coals due to the fixation of pyrite in marine-influenced coal-forming environments. The occurrence of pyrite accounts for the association of a large number of elements (Fe, S, As, Cd, Co, Cu, Mn, Mo, Ni, Pb, Sb, Se, and Zn) with sulphides, as deduced from the analysis of the density fractions. The marine influence is probably also responsible for the organic association of B. The REEs, Zr, Nb, and Hf, are enriched by a factor of 2–3 with respect to the highest levels fixed for the usual worldwide concentration ranges in coal for these elements. The content of these elements in the Late Permian coal is higher by a factor of 5–10 with respect to the Late Triassic coal. Furthermore, other elements, such as Cu, P, Th, U, V, and Y, are relatively enriched with respect to the common range values, with maximum values higher than the usual range or close to the maximum levels in coal. The content of these elements in the Late Permian coal is higher than the Late Triassic coal. These geochemical enrichments are the consequence of the occurrence, in relatively high levels, of phosphate minerals, such as apatite, xenotime, and monazite, as deduced from the study of the density fractions obtained from the bulk coal.The Late Triassic coal has a low sulphur content with a major organic affinity. The trace element contents are low when compared with worldwide ranges for coal. In this coal, the trace element distribution is governed by clay minerals, carbonate minerals, and to a lesser extent, by organic matter and sulphide minerals.Major differences found between late Permian and Triassic coals are probably related to the source rocks, given that the main source rock of the late Permian epicontinental marine basin is the Emeishan basalt formation, characterised by a high phosphate content.     

Coal geology and coal quality of the Miocene Mugla basin, southwestern Anatolia, Turkey

This work focuses on the relationship between the coal geology and coal quality of the Miocene Mugla basin, Southwestern Anatolia, Turkey. To this end, detailed petrographical, mineralogical and geochemical studies were performed on composite profile samples from the nine coal fields in the Mugla basin (Alatepe, Bagyaka, Bayir, Çakiralan, Ekizköy, Eskihisar, Hüsamlar, Sekköy and Tinaz coal fields). The Mugla lignite is a high ash (from 16 to 56%) and sulphur (from 2.1 to 5.7%) lignite which is petrographically characterised by a high huminite content, mainly gelinite macerals. The mineral matter of the studied lignite samples is made up mainly of clay minerals and quartz, with the exception of the Sekköy and Ekizköy lignites, in which calcite is the dominant mineral phase with minor amounts of quartz, clay minerals, pyrite and gypsum and traces of aragonite. Syngenetic opal is also frequently identified in these samples. The differentiation of these two types of lignite with specific mineralogical patterns is attributed to the contemporaneous development of peatlands with a high detrital input, dominated by the quartz and clay mineral setting, and peatlands with low detrital supply and a dominant carbonate-rich lacustrine environment. The higher water table of the latter allowed the precipitation of micritic carbonates and the development of lakes with abundant mollusc fauna. This differentiation is also evidenced by the geochemical data. Thus, the Sekköy, Ekizköy, Hüsamlar, Bayir and Alatepe lignites are characterised by relatively low Al and Fe contents (<1.4%) and high sulphur contents (4.2 to 5.7%). In addition Sekköy and Ekizköy show relatively high contents of Ca (6.3–7.1% compared to 1.6–3.8% in the other lignites). All the lignite samples studied are characterised by relatively high Mo and U contents when compared with the worldwide averages of trace elements in coal. Relatively high alkaline syngenetic conditions of the peat-forming environment of the Mugla coal are deduced from the following mineralogical, petrographical and geochemical evidence: (a) the precipitation of syngenetic opal (dissolution of quartz and re-precipitation as opal) and calcite; (b) minor and very early syngenetic sulphide precipitation (only framboidal and euhedral pyrite); (c) high bacterial activity, typical of high pH conditions, inferred from low preservation of tissue structures; (d) preservation of aragonite gastropod shells; and (e) the anomalous enrichment of U, Mo and W. A key result of the study of Mugla limnic coals (at least of the Sekköy and Ekizköy coal fields) is that a major influence was exerted on the early diagenetic evolution of the coal by the hydrochemistry of the lacustrine waters. This hydrochemistry was largely linked to the lithology of the surrounding source rock areas although the final evolutionary trend of the solute composition in the lake waters, characterized by very high carbonate and sulphate contents, was largely enhanced by the endorheic river drainage system and the arid–semiarid paleoclimatic situation under which organic matter accumulation took place.