Element mobility during pyrite weathering: implications for acid and heavy metal pollution at mining-impacted sites   总被引：1，自引：0，他引：1  

Long Lu  Rucheng Wang  Fanrong Chen  Jiyue Xue  Peihua Zhang  Jianjun Lu 《Environmental Geology》2005,49(1):82-89

Based on back scattered electron images and electron micro-probe analysis results, four alteration layers, including a transition layer, a reticulated ferric oxide layer, a nubby ferric oxide layer and a cellular ferric oxide layer, were identified in the naturally weathering products of pyrite. These layers represent a progressive alteration sequence of pyrite under weathering conditions. The cellular ferric oxide layer correlates with the strongest weathering phase and results from the dissolution of nubby ferric oxide by acidic porewater. Leaching coefficient was introduced to better express the response of element mobility to the degree of pyrite weathering. Its variation shows that the mobility of S, Co and Bi is stronger than As, Cu and Zn. Sulfur in pyrite is oxidized to sulfuric acid and sulfate that are basically released into to porewater, and heavy metals Co and Bi are evidently released by acid dissolution. As, Cu and Zn are enriched in ferric oxide by adsorption and by co-precipitation, but they would re-release to the environment via desorption or dissolution when porewater pH becomes low enough. Consequently, Co, Bi, As, Cu and Zn may pose a substantial impact on water quality. Considering that metal mobility and its concentration in mine waste are two important factors influencing heavy metal pollution at mining-impacted sites, Bi and Co are more important pollutants in this case.  相似文献   

A high-resolution TEM-AEM, pH titration, and modeling study of Zn coprecipitation with ferrihydrite     

Stacin Martin  Chen Zhu  Joseph Rule  Robert Ford  Yee Soong 《Geochimica et cosmochimica acta》2005,69(6):1543-1553

Experiments of Zn²⁺ and Fe³⁺ coprecipitation as a function of pH were conducted in the laboratory at ambient temperature and pressure. X-ray diffraction patterns of the coprecipitates show two broad peaks at 0.149 and 0.258 nm, which is consistent with published patterns for pure 2-line ferrihydrite. Zn²⁺ uptake occurred at pH ≥5 while Fe³⁺ precipitation occurred between pH 3 and 4, although both Zn²⁺ and Fe³⁺ were present in the same solution during the entire range of pH titration. High-resolution transmission electron microscopy shows that the coprecipitates are 2 to 6 nm sized single crystalline particles but aggregated to 50 to 400 nm sized clusters. Analytical electron microscopy indicated that the 5% atomic Zn with respect to Fe was homogeneously distributed. No segregated phases were found in the clusters or at single crystal edges, which is consistent with published extended X-ray absorption fine structure (EXAFS) results at similar Zn/(Zn + Fe) ratios. Hence, occlusion and surface precipitation may be excluded as possible coprecipitation mechanisms. The bulk solution Zn²⁺ sorption edge was fitted to both solid solution and generalized diffuse layer surface complexation models. However, a solid solution model is inconsistent with published EXAFS results that show tetrahedral polydentate Zn²⁺ complexes sharing apices with Fe³⁺octahedra.  相似文献   

In situ feldspar dissolution rates in an aquifer   总被引：1，自引：0，他引：1  

Chen Zhu 《Geochimica et cosmochimica acta》2005,69(6):1435-1453

In situ silicate dissolution rates within the saturated Navajo sandstone, at Black Mesa, Arizona were determined from elemental fluxes in the aquifer. The mass transfer between groundwater and mineral matrix along flow paths was calculated from inverse mass balance modeling. The reaction time is bound by ¹⁴C-based travel time. BET surface areas were measured with N₂ gas adsorption. Dissolution rates for K-feldspar and plagioclase are 10⁻¹⁹ and 10⁻¹⁶ mol (feldspar) m⁻² s⁻¹, respectively, which are ∼10⁵ times slower than laboratory experiment-derived rates under similar pH and temperature but at far from equilibrium conditions. The rates obtained in this study are consistent with the slower field rates found in numerous watershed and soil profile studies. However, these rates are from saturated aquifers, overcoming some concerns on estimated rates from unsaturated systems. The Navajo sandstone is a quartz-sandstone with a relatively simple and well-studied hydrogeology, groundwater geochemistry, and lithology, a large number of groundwater analyses and ¹⁴C groundwater ages, groundwater residence times up to ∼37 ky, groundwater pH from ∼8 to 10, and temperature from ∼15 to 35°C.  相似文献   

Erratum to B. Chen and Y. Arakawa (2005) “Elemental and Nd-Sr isotopic geochemistry of granitoids from the West Junggar foldbelt (NW China), with implications for Phanerozoic continental growth”, Geochimica et Cosmochimica Acta 69, 1307-1320     

Bin Chen 《Geochimica et cosmochimica acta》2005,69(22):5387-5388

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午后多重极光弧观测研究          下载免费PDF全文

温艳波  杨惠根  韩德胜  T.Araki  艾勇  刘瑞源  刘勇华  胡泽骏  陈卓天  邓忠新  刘嵘  王晶 《极地研究》2005,17(4):255-263

本文利用2001-2003年南极中山站175天全天空摄像机观测,对午后多重极光弧的出现率及其与Kp指数的关系进行了统计分析,结果表明午后多重极光弧出现率呈一单峰分布,最大发生率出现在1445UT(1645MLT),其位置在1500MLT极光热点(1300-1700MLT)近夜侧的部分。与地磁活动指数Kp的相关统计分析表明,Kp值为2-3之间时多重极光弧有较大的出现率,这说明中等地磁活动情形下午后多重极光弧有较高的出现率。事件分析表明多重极光弧的强度变化与地磁Pc5脉动具有较高的相关性,并且有类似的频谱特征,这说明午后多重极光弧可能与同时出现的Pc5地磁脉动有关。  相似文献   

1952~2003年我国区域经济发展不均衡的 长期变化态势   总被引：2，自引：1，他引：2  

郭腾云  徐勇 《地理科学进展》2005,24(1):21-30

文中分别利用Gini、GE等指数，以实际人均国内生产总值(GDP)为指标，详细考查了从1952~2003年，我国省市区间经济发展不均衡的变化态势及其在东部-内陆、南方-北方、高城镇化-低城镇化地区等方向上的变化。人均实际GDP的Gini、GE等指数显示，从1952~2003年，我国省级区域经济发展不均衡的总体态势是以较缓慢的速度逐步增加。具体的变化是，随着时间的推移区域经济不均衡呈周期性地上升、下降运动。就我国省市区经济发展不均衡在空间上的变化而言，一是在沿海-内陆和高城镇化-低城镇化方向上，分别在1990s中期和1980s中期以前，我国省市区经济不均衡主要表现为区域内部不均衡，但区域之间不均衡则不断增加，并逐步成为省市区经济不均衡主要部分；一是，在北方-南方方向上，我国省市区经济不均衡则是一直表现为区域内部不均衡，区域之间不均衡对省市区经济不均衡的贡献一直显得微不足道。  相似文献   

青藏高原腹地植物碳同位素组成对环境条件的响应   总被引：7，自引：0，他引：7  

王谋  李勇  黄润秋  李亚林  张玉修 《山地学报》2005,23(3):274-279

现代植物碳同位素组成是特定环境影响的结果,通过对植物碳同位素组成的研究可以揭示植物生长期环境信息。针对青藏高原腹地高寒草甸~高寒草原过渡区植被碳同位素组成进行研究;该区高山嵩草样δ13C值在-25.63‰~-27.95‰间,平均值-26.63‰;高寒草原区混合样δ13C值于-26.29‰~-27.73‰间,平均值-27.04‰。高山嵩草样δ13C值总体呈现由南东往北西方向正偏趋势,研究区北部高寒草原区混合植物样也呈现出由南向北富重碳同位素趋势。这些变化规律被认为是主要受降水环境影响的结果,而区域内降水条件的展布规律则是受高原夏季风运移方式的控制。对植物δ13C值与地理位置的回归分析表明,该区植被碳同位素组成与地理位置相关,高山嵩草样(r=0.44603,n=29,p<0.05)和混合样(r=0.8112,n=5,p<0.1)均表现出对区域降水环境条件的良好响应。据此,以该区植物δ13C值为背景,进行合理推算,拟定了研究区内干旱区和湿润区界限的位置。  相似文献   

Semi-analytical and Numerical Studies on the Flattened Brazilian Splitting Test Used for Measuring the Indirect Tensile Strength of Rocks     

Y. G. Huang  L. G. Wang  Y. L. Lu  J. R. Chen  J. H. Zhang 《Rock Mechanics and Rock Engineering》2015,48(5):1849-1866

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Fracture mechanics analysis of multiple cracks in anisotropic media     

Chia‐Huei Tu  C.‐S. Chen  T.‐T. Yu 《国际地质力学数值与分析法杂志》2011,35(11):1226-1242

This paper presents a single‐domain boundary element method (BEM) for linear elastic fracture mechanics analysis in the two‐dimensional anisotropic material. In this formulation, the displacement integral equation is collocated on the un‐cracked boundary only, and the traction integral equation is collocated on one side of the crack surface only. A special crack‐tip element was introduced to capture exactly the crack‐tip behavior. A computer program with the FORTRAN language has been developed to effectively calculate the stress intensity factors of an anisotropic material. This BEM program has been verified having a good accuracy with the previous researches. Furthermore, by analyzing the different anisotropic degree cracks in a finite plate, we found that the stress intensity factors of crack tips had apparent influence by the geometry forms of cracks and media with different anisotropic degrees. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

Chemical weathering and CO2 consumption in the glaciated Karuxung River catchment,Tibetan Plateau     

Fan Zhang  Xiong Xiao  Lijie Wang  Chen Zeng  Zhengliang Yu  Guanxing Wang  Xiaonan Shi 《水文研究》2021,35(8):e14330

Climate factors play critical roles in controlling chemical weathering, while chemically weathered surface material can regulate climate change. To estimate global chemical weathering fluxes and CO₂ balance, it is important to identify the characteristics and driving factors of chemical weathering and CO₂ consumption on the Tibetan Plateau, especially in glaciated catchments. The analysis of the hydro-geochemical data indicated that silicate weathering in this area was inhibited by low temperatures, while carbonate weathering was promoted by the abundant clastic rocks with fresh surfaces produced by glacial action. Carbonate weathering dominated the riverine solute generation (with a contribution of 58%, 51%, and 43% at the QiangYong Glacier (QYG), the WengGuo Hydrological Station (WGHS), and the lake estuary (LE), respectively). The oxidation of pyrite contributed to 35%, 42%, and 30% of the riverine solutes, while silicate weathering contributed to 5%, 6%, and 26% of the riverine solutes at the QYG, WGHS, and LE, respectively. The alluvial deposit of easily weathering fine silicate minerals, the higher air temperature, plant density, and soil thickness at the downstream LE in comparison to upstream and midstream may lead to longer contact time between pore water and mineral materials, thus enhancing the silicate weathering. Because of the involvement of sulfuric acid produced by the oxidation of pyrite, carbonate weathering in the upstream and midstream did not consume atmospheric CO₂, resulting in the high rate of carbonate weathering (73.9 and 75.6 t km⁻² yr⁻¹, respectively, in maximum) and potential net release of CO₂ (with an upper constraint of 35.6 and 35.2 t km⁻² yr⁻¹, respectively) at the QYG and WGHS. The above results indicate the potential of the glaciated area of the Tibetan Plateau with pyrite deposits being a substantial natural carbon source, which deserves further investigation.  相似文献