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31.
ZHANG Huan LUO Taiyi GAO Zhenmin MA Deyun TAO Yan 《中国地球化学学报》2007,26(4):439-445
Studies on the helium, lead and sulfur isotopic composition were performed of the Gejiu super-large Sn-polymetallic ore deposit. The results indicated that the ore-forming materials came from different sources and the deposit is a product of superimposed mineralization. The deposit is characterized by multi-source and multi-period mineralization, which experienced submarine hydrothermal deposition and Late Yanshanian magmatic hydrothermal mineralization. It is held that the Gejiu super-large Sn-polymetallic ore deposit is a multi-genesis deposit. 相似文献
32.
Oxidant-elemental sulfur as an effective promoter for transformation of organic matter to hydrocarbons at moderate-low temperatures 总被引：1，自引：0，他引：1
Elemental sulfur is widely dispersed in the hydrocarbon source rocks and its depositional environment is usually thought as a reducing environment. The presence or absence of free oxygen is a key to identify oxidizing or reducing environment. But elemental sulfur is often present as an oxidant in this environment. When elemental sulfur meets with organic matter, redox reaction will occur. In our simulation experiments at 200 -400℃ , the existence of elemental sulfur can sharply increase the amounts of hydrocarbons, hence leading to the production of immature or low-mature oils and natural gases. At the temperature of 300℃ , the addition of elemental sulfur will further enhance the relative yields of hydrocarbons,and the final yield of total extracts and gaseous hydrocarbons of similitude kerogens by more than 463% and 2760% , respectively, while those of oil shales are increased by about 71% and 2044% , respectively. But at the temperature of 450℃, elemental sulfur plays a negative role in liquid hydrocarbon formation. The presence of elemental sulfur is probably a key factor in the gypsolyte environment leading to the formation of immature or low-mature oils, as well as the coexistence of immature or low-mature oils and natural gases. 相似文献
33.
Martin Kralik Franko Humer Johannes Grath Johanna Nurmi-Legat Andrea Hanus-Illnar Stan Halas Monika Jelenc 《中国地球化学学报》2006,25(B08):154-155
The impact of air pollution is a substantial European and global problem which has been observed even in the most remote areas of our planet. Not only surface water, but also groundwater resources are partly endangered by dry and wet deposition from the air. Karst and other sensitive aquifers contribute up to 90 % to the total drinking water supply in some European regions. However, they are more vulnerable to contamination than other aquifers due to short transfer times from recharge to source. Therefore, the main objective of this paper is to show possibilities to quantify the impact of air pollution on sensitive water resources （e.g. karst）, to develop an innovative surveillance tool based on isotopes and meteorological considerations. Comparisons of lead isotope measurements in precipitation, spring waters, soil profiles and dolomite bedrock in a relatively pristine and remote area at the front-range of the Northern Calcareous Alps in Austria with literature data indicate that radiogenic Australian gasoline-lead still dominates with 60%-80% the composition of the trace lead in the spring waters. In addition to the lead leached from the dolomite bedrock a third source contributes about 5%-10%. This second long distance Pb-contribution may originate from coal burning and/or Ag-Pb-ore smelting in central Europe in the past. The monthly precipitation （May and September 2005） samples show ^18O-rich sulphate ions, whereas the soil sulphates change in the direction to lower ^18O- and higher ^34S values with depth. The spring waters and bedrock dolomites show relatively low delta ^34S values （4‰-9 ‰）. Assuming the precipitation samples and the dolomite bed rocks are end-members the contribution of atmospheric sulphate can estimated to be 20% in the spring waters and between 10% to 45% in the soil samples. The ^87Sr/^86Sr-isotope results in the precipitation （0.7092） support at least a more radiogeradiogenic, far transported source in addition to a possible recycling of local dolomite and limestone （0.7080-0.7083） dust. 相似文献
34.
Yunchao LANG Congqiang LIU Jianghong WU Hiroshi Satake Siliang LI 《中国地球化学学报》2006,25(B08):173-173
A groundwater system in a karstic terrain is easily subject to pollution and its remediation is difficult once contaminated by human activities. The groundwater samples collected in both winter and summer seasons at Guiyang, SW China, show a wide range of variations in chemical composition and dominance of Ca^2＋, Mg^2＋, SO4^2-, and HCO3^- ions. The anthropogenic inputs include Cl^-, NO3^-, SO4^2-, Na^＋, and K^＋, as judged from the relationships between different elemental ratios and sewage samples. Cl^- concentrations of all water samples in the study area vary from 0 to 3.9 mmol/L in winter and are higher than in summer. In most of the samples, SO4^2- concentrations are high, ranging from 0.1 to 11 mmol/U The studies show that the cycling of sulfur plays an important role in controlling water chemistry and fate of contaminants in groundwater. In order to understand the source of SO4^2- and the geochemical cycling of some elements in the karstic groundwater environment, we have carried out a study on the variations of S and Cl isotope compositions, in addition to other isotopic tracers such as ^87Sr/^86Sr and δ^13C studied previously. The δ^37Cl values of the groundwater samples present a seasonal variation, ranging from 0.00‰ to ＋2.03‰ in winter and from -1.46‰ to ＋0.29‰ in summer. The surface water samples show a similar range of variations as observed for groundwater. Two rainwater samples collected at Guiyang have a distinct isotopic signature （mean value is -3‰） compared to the δ^37Cl values reported in literature. These results indicate that ground water is mainly derived from precipitation and suggest a fast recharge of the karst system by surface water. 相似文献
35.
Chenlin CHOU 《中国地球化学学报》2006,25(B08):82-82
Hazardous air pollutants, including compounds of sulfur and toxic trace elements, are emitted during coal combustion. Geochemical studies of these constituents in coals provide information about their species, regional distribution and origins. The data are useful in understanding the cause and scope of human health problems related to these hazardous elements and in designing preventive or remedial measures. Sulfur in coal is a problem because sulfur dioxide emitted during coal combustion is a main source of acid rain. The sulfur isotopic evidence shows that sulfur in low-sulfur coal is derived primarily from parent plant materials. Sulfur enrichment in medium- and high-sulfur coals is caused by the sulfate in seawater that flooded the peat swamp during coal formation. The sulfur content of a coal is controlled primarily by the depositional environment of coal seams. Only pyritic sulfur can be removed by physical coal cleaning processes （coal preparation）. Sulfur dioxide emission can be reduced using clean coal technologies, such as flue-gas desulfurization, fluidized-bed combustion, and integrated gasification and combined cycle. 相似文献