An electrochemical study of pyrite oxidation in the presence of carbon coatings in cyanide medium     

H. Tan  D. Feng  J.S.J. van Deventer  G.C. Lukey 《International Journal of Mineral Processing》2006,80(2-4):153-168

The anodic and cathodic behaviour of pyrite with clay and different carbon coatings of activated carbon, graphite and carbonaceous matter in cyanide medium was investigated using the potentiodynamic method. The presence of clay coating did not change the polarisation curve appearance for either the anodic oxidation of pyrite or the cathodic reduction of oxygen or the potential of the current plateau, but only decreased the plateau current especially at a higher coating thickness. The presence of the carbon coatings marginally shifted the rest potential for pyrite to a more anodic position and slightly changed the polarisation curve appearance for pyrite oxidation. The current density for pyrite oxidation largely increased in the presence of the carbon coatings, the potential at the plateau shifted to more cathodic positions, and the plateau width became smaller. These effects became more noticeable at a higher coating thickness. The activated carbon, graphite and carbonaceous matter coatings performed similarly in affecting pyrite oxidation at a similar thickness. The carbon coatings significantly increased the limiting current densities for oxygen reduction on pyrite, and the limiting current plateau became steeper at a higher coating thickness. The carbon coatings increased the limiting current density for oxygen reduction to a similar extent at a low coating thickness, but increased to varied extents at a higher coating thickness. The carbon coatings also greatly increased the cathodic current density for gold reduction on pyrite. The enhancement of pyrite oxidation and oxygen or gold reduction on pyrite by the carbon coatings was likely attributed to the electrochemical interaction between pyrite and the carbon materials with electron-rich surfaces and high conductivity. The presence of the carbon coatings significantly increased the oxidation of pyrite in aerated cyanide solutions and the preg-robbing of pyrite especially at a higher coating thickness.  相似文献   

The effects of carbon dioxide leakage on fractures, and water quality of potable aquifers during geological sequestration of CO2     

Wei ZHANG Yilian LI Tianfu XU Wei QIANG Shangping XIAO 《中国地球化学学报》2006,25(B08):58-58

Since industrial revolution, the ＂greenhouse effect＂ is one of the most important global environmental issues. Of all the greenhouse gases, CO2 is responsible for about 64% of the enhanced ＂greenhouse effect＂, making it the target for mitigation, so reducing anthropogenic discharge of carbon dioxide attracts more and more attention. Geological sequestration of CO2 in deep saline aquifers is one of the most promising options. But because unknown fractures and faults may exist in the caprock layers which can prevent the leakage of CO2, CO2 will leak upward into upper potable aquifers, and lead to adverse impacts on the shallow potable aquifers. In order to assess the potential effect of CO2 leakage from underground storage reservoirs on fractures and water quality of potable aquifers, this study used the non-isothermal reactive geochemical transport code TOUGHREACT developed by Xu et al to establish a simplified 2-D model of CO2 underground sequestration system, which includes deep saline aquifers, caprock layers, and shallow potable aquifers, and study and analyze the changes of mineral and aqueous components. The simulation results indicated that the minerals of deep saline aquifers and fractures should be mainly composed of aluminosilicate and silicate minerals, which not only enhance the mass of CO2 sequestrated by mineral trapping, but also decrease the porosity and permeability of caprock layers and fractures to prevent and reduce CO2 leakage. The results from deep saline aquifers showed that the mass of carbon dioxide trapped by minerals and solution phases is limited, the rest remained as a supercritical phase, and so once the caprock aquifers have some unknown fractures, the free carbon dioxide phase may leak from CO2 geologic sequestration reservoirs by buoyancy.  相似文献   

Integrated stratigraphy and paleoenvironmental reconstruction of the Miocene series of the Chateauredon Dome, S.E. France     

Anne Bialkowski  Jean-Jacques Chateauneuf  Isabelle Cojan  Hugues Bauer 《Eclogae Geologicae Helvetiae》2006,99(1):1-15

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紫色丘陵区不同土地利用方式下土壤活性有机碳垂直分布特征     

《山地学报》2006,24(B10):21-26

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环溪河流域土壤氮素含量及影响因素分析     

黄海峰邓良基  胡玉福高雪松 郑小佳 《山地学报》2006,24(B10):98-102

根据67个随机格网样点和分层抽样样点的耕层土壤氮素含量，在ArcGIS9．0平台上运用地统计学等方法研究了环溪河流域土壤氮素含量及其影响因素。结果表明，环溪河流域土壤全氮和碱解氮的平均含量分别为0．60g／kg和53．31mg／kg。研究区土壤全氮含量总体上呈条带状和团块状分布，其低值中心区（〈0．5g／kg）位于团结村不规则三角形区域，并以此为中心向四周增加；高值中心区（〉0．8g／kg）主要位于走马村椭圆状区域。区内土壤碱解氮其高值区（〉75mg／kg）主要分布在深弯村以西，低值区（〈33mg／kg）主要分布于窝窝店村和杨柳村一带。影响区内土壤氮素含量空间分布的因素主要是成土母质、土壤质地、土地利用方式、地貌和坡度。  相似文献   

森林碳汇决策与农村可持续发展研究(英文)     

殷永元  徐伟 《福建地理》2006,(3)

认为有必要在基于碳汇的土地利用和当地可持续发展之间建立一种更加明确的联系.依托一个中国-加拿大合作项目,以中国贵州省黎平县为例,阐述了一种将森林碳汇、森林资源管理以及如何促进当地可持续发展联系起来的综合评估方法,并且着重介绍了能帮助资源管理和规划部门实施这种综合评估的土地利用决策支持工具(LUDST) .  相似文献   

湿地生态系统碳循环过程及碳动态模型     

仝川  曾从盛 《福建地理》2006,(3)

从地上、地下有机物质生产对湿地碳输入的贡献,湿地土壤碳库以及土地利用变化对湿地土壤碳库和碳排放的影响,甲烷排放和可溶性有机碳输出以及影响因子,湿地生态系统碳循环动态模型4个方面对湿地生态系统碳循环国内外研究进展和研究成果进行综述、分析,提出了我国亚热带区域天然湿地碳循环研究的主要热点和方向:⑴沿海湿地碳库估算及土地利用转化对土壤碳库和温室气体排放的影响;⑵酸沉降对于我国东南沿海低纬度地区湿地甲烷排放的影响;⑶沿海湿地生态系统碳循环动态模型的应用与开发;⑷湿地系统可溶性有机碳的输出机理探讨.  相似文献   

大气CO2浓度升高对土壤中不同粒级碳的影响   总被引：4，自引：0，他引：4  

马红亮朱建国  谢祖彬刘钢 曾青 《亚热带资源与环境学报》2006,1(1):33-40

不同粒级土壤中的碳有着不同的周转规律，在高CO2浓度条件下，它们含量的变化将在一定程度上反映土壤碳是累积还是减少，对明确土壤碳的变化趋势有重要意义．采用田间培养试验初步模拟研究在高CO2浓度条件下土壤不同粒级碳的分布．结果表明，加入秸秆培养1年，由于CO2浓度升高的原因导致在低氮（LN）、常规氮（NN）和高氮（HN）水平下土壤中碳分别增加0．01、1．10、1．22g／kg，表现为粒级〈53μm土壤颗粒中碳分别增加1．53、2．19、2．70g／kg．粒级〈53μmm土壤颗粒碳量的增加，主要是由于其重量分配百分数显著增加36．2％，碳浓度增加5．4％；粒级〉250μm和250～53μm土壤颗粒部分虽然其碳浓度分别增加20．8％和17．3％（P〈0．05），怛由于重量分配百分数分别显著降低22．8％和36．1％，结果碳量降低．试验表明高CO2浓度导致不同粒级土壤的分配及碳浓度的变化；高氮施肥水平下有增加土壤碳量特别是小粒级土壤碳量的趋势．  相似文献   

森林碳汇决策与农村可持续发展研究     

殷永元  徐伟 《亚热带资源与环境学报》2006,1(1):51-62

认为有必要在基于碳汇的土地利用和当地可持续发展之间建立一种更加明确的联系．依托一个中国-加拿大合作项目，以中国贵州省黎平县为例，阐述了一种将森林碳汇、森林资源管理以及如何促进当地可持续发展联系起来的综合评估方法，并且着重介绍了能帮助资源管理和规划部门实施这种综合评估的土地利用决策支持工具（LUDST）．  相似文献   

Retrieval of stratospheric O3 and NO2 vertical profiles using zenith scattered light observations     

G. S. Meena  C. S. Bhosale  D. B. Jadhav 《Journal of Earth System Science》2006,115(3):333-347

Daily zenith scattered light intensity observations were carried out in the morning twilight hours using home-made UV-visible spectrometer over the tropical station Pune (18‡31′, 73‡51′) for the years 2000–2003. These observations are obtained in the spectral range 462–498 nm for the solar zenith angles (SZAs) varying from 87‡ to 91.5‡. An algorithm has been developed to retrieve vertical profiles of ozone (O₃) and nitrogen dioxide (NO₂) from ground-based measurements using the Chahine iteration method. This retrieval method has been checked using measured and recalculated slant column densities (SCDs) and they are found to be well matching. O₃ and NO₂ vertical profiles have been retrieved using a set of their air mass factors (AMFs) and SCDs measured over a range of 87–91.5‡ SZA during the morning. The vertical profiles obtained by this method are compared with Umkehr profiles and ozonesondes and they are found to be in good agreement. The bulk of the column density is found near layer 20–25 km. Daily total column densities (TCDs) of O₃ and NO₂ along with their stratospheric and tropospheric counterparts are derived using their vertical profiles for the period 2000–2003. The total column, stratospheric column and tropospheric column amounts of both trace gases are found to be maximum in summer and minimum in the winter season. Increasing trend is found in column density of NO₂ in stratospheric, tropospheric and surface layers, but no trend is observed in O₃ columns for above layers during the period 2000–2003  相似文献