Platinum-group element distribution in chromite ores from ophiolite complexes: implications for their exploration     

Maria Economou-Eliopoulos 《Ore Geology Reviews》1996,11(6):363-381

Compilation of some new data on ophiolites for Greece and Yugoslavia, and published data from previous studies, indicate that platinum-group element (PGE) and gold concentrations in chromite ores are generally low, ranging from less than 100 ppb to a few hundred ppb. However, samples from several ophiolite complexes exhibit an enrichment (of a few ppm) (a) only in Os, Ir and Ru,(b) only in Pt and/or Pd or (c) in all PGE. This enrichment (up to 10s ppm) is mainly related with chromitites hosted in supra-Moho dunites and dunites of the uppermost stratigraphic levels of the mantle sequence and it seems to be local, independent of the chromitite major element composition and the chromite potential of the ophiolite complexes. The contents of PGE combined with less chalcophile elements (Ni, Co, Cu), the ratios of incompatible/compatible elements, and PGE-patterns provide evidence for discrimination between chromitites derived from primitive magmas and those derived from partially fractionated magmas, although they have a similar major element composition. Thus, they can be used for a stratigraphic orientation in the mantle sequence, and therefore for exploration targets. Moreover, PGE data offer valuable information for the evaluation of the chromite potential in ophiolite complexes. The most promising ophiolites seem to be those which apart from the petrological and geochemical characteristics indicating extensive degree of partial melting in the mantle source contain only one chromite ore type (the other type being only in small proportion) of limited compositional variation, in both major elements and PGE, low ratios of , while PGE-enriched chromitites in the mantle sequence are only occasionally present. In contrast, ophiolites which contain both high-Cr and -Al chromitites, and where their chalcophile element data implies relatively extensive fractionation trend are not good exploration targets for chromite ores, although they are related with a SSZ environment.  相似文献   

化探背景与异常划分中的C型转换法     

陈明  范继璋  矫希国 《吉林大学学报(地球科学版)》1996,(2)

化学背景与异常在统计学上的差异同时表现在浓度和变差两个方面。在划分背景与异常时,把这两方面信息提取出来并作显化处理,使背景与异常的差别更大,以利划分,这就是Ｃ型转换的基本思想。介绍了Ｃ型转换法的基本原理及其在条件模拟和实际金矿区中的应用。  相似文献   

Intrinsic sample methods for mineral exploration and resource assessment     

DeVerle Harris  Guocheng Pan 《Natural Resources Research》1993,2(2):113-121

We report on an objective methodology, referred to as intrinsic sample methodology, for the delineation of exploration target areas or resource areas for assessment. Important features of the methodology include (1) identification of recognition criteria for critical genetic factors, (2) synthesis of new variables from enhanced geodata, (3) estimation of logit probability models, and (4) cutting of estimated logit probabilities to delineate exploration targets or resource areas. The methodology is demonstrated on the Walker Lake quadrangle of Nevada and California.  相似文献   

深部矿产资源立体地球化学勘查方法技术体系     

史长义  王惠艳 《地质学报》2022,96(11):3705-3721

深部矿产资源的勘查是战略性矿产资源勘查的一个重要方面。找矿实践证明，化探方法技术在矿产勘查乃至深部找矿中发挥了重要的、不可或缺的作用。找矿工作的不断深入和找矿难度的不断加大，促使化探方法技术不断的发展和完善，在传统方法技术的基础上，研发出了许多新的方法技术。本文从方法论和系统论的角度出发，对现有的找寻深部隐伏矿盲矿的有效化探方法技术进行了系统的归纳和总结，提出了立体地球化学勘查方法技术体系的概念，将立体地球化学勘查方法技术划分为地面地球化学测量方法技术和地下地球化学测量方法技术，建立了深部矿产资源立体地球化学勘查方法技术体系。不同的方法技术有不同的优势和不同的适用条件，实际工作中应当根据不同的勘查阶段，不同的勘查目的和不同的地质地球化学条件选择不同的立体方法技术组合才能发挥出最大效益，取得最大效果。  相似文献   

碳中和目标下关键矿产在清洁能源转型中的作用、供需分析及其建议          下载免费PDF全文

王欢  马冰  贾凌霄  于洋  胡嘉修  王为 《中国地质》2021,48(6):1720-1733

在"碳中和"目标的驱动下，全球能源系统向清洁化、低碳化甚至无碳化发展已是大势所趋。针对向清洁能源转型的需求，采用了统计对比、分类汇总、综合分析等方法，分析研究了关键矿产在电池、电网、低碳发电和氢能等行业中的作用和需求。结合当前关键矿产产量的地理集中度高、项目开发周期长、资源质量下降等矿产供应和投资计划不能满足清洁能源转型的需求等问题，提出确保关键矿产多样性供应，推动价值链各环节的技术创新，扩大回收利用，增强供应链弹性和市场透明度，将更高的环境、社会和治理标准纳入主流程及加强生产者和消费者之间的国际合作等建议。  相似文献   

重视和加强岩矿物性的测量研究     

蒋宏耀  张立敏 《地球物理学进展》1995,10(3):118-123

本文从物探科学技术的进步,勘查任务的发展变化、物探方法应用范畴的扩大和物性勘探等几个方面,论述了岩石和矿物物理性质测量、研究的重要性,指出：物性工作不可能毕其功于一役,并提出了五点建议：１．深入研究各类矿藏及其围岩（直至地面）物性的空间变化规律,为选择、研究合适的物探方法,提高物探效果,进一步探讨“直接”找矿问题,提供依据;２．这项工作可专门进行,但最好尽可能利用为其他目的而设计的钻井进行;３．物  相似文献   

我国勘查地球物理的若干进展─1994年   总被引：1，自引：0，他引：1  

陈云升 《物探与化探》1995,19(6):401-414

1994年,我国固体矿产地球物理工作仍不景气,水文、工程、环境地球物理市场平稳,油气地球物理工作持续增长.陆上三维地震年工作量首次超过一万平方公里.高山、大沙漠地区三维地震采集创造成功经验,地震数据全三维处理、解释技术和软件系统的研究和应用取得显着进展.航空地球物理工作量略有回升.总体上1994年我国各类勘查地球物理方法在“硬件”(仪器设备)方面的新进展相对较少,而在“软件”(方法技术特别是数据处理、解释技术)的研究、应用方面则取得较多重要进展.  相似文献   

综合利用地震多参数预测油气藏     

杨丙中  邓俊国 《吉林大学学报(地球科学版)》1990,(3)

以吉林省境内红星构造带(已发现油田)和杨柳青构造带(未发现油田)为试验区,首先利用地震地层学方法,研究间接参数特征,确定有利相带和有效圈闭,并在有效圈闭上选择了39个2×2cm时窗。在时窗内提取与地震波动力学有关的信息,即频率、振幅、频谱能量等,然后对这种信息进行统计计算,获得振幅方差等九个参数并对其进行综合分析,从已知油气藏出发,对未知圈闭油气状况进行了三级预测,指出了最有利的勘探靶区。  相似文献   

Changes in manganese and lead in the environment and young children associated with the introduction of MMT in gasoline     

Brian Gulson Karen Mizon Michael Korsch Honway Louie Michael Wu Jenny Stauber J. Michael Davis Alan Taylor 《中国地球化学学报》2006,25(B08):62-62

This is a 4-year longitudinal study to evaluate changes to the environment and exposure of young children associated with the introduction of methylcyclopentadienyl manganese tricarbonyl （MMT） into Australia in 2000. The cohort includes 57 females and 56 males; age range of 0.29 to 3.9 years. Samples are collected every 6 months from children in residences located at varying distances from major traffic thoroughfares in Sydney. Environmental samples： air, house and day care dustfall, soil, dust sweepings and gasoline. Samples from children： blood, urine, handwipes prior to and after playing outdoors, and a 6-day duplicate diet. All samples are analyzed for a suite of 20 elements using ICP-MS. Results are presented for the first three 6-month sampling periods for Pb and Mn. For dustfall accumulation, there was no significant change over the 3 sampling periods （time） for Pb or Mn, and a positive relationship between ‘traffic exposure＇ （traffic volume and proximity to the road） and Pb but not Mn. For handwipes, Pb and Mn in wipes taken from children after playing outdoors were usually significantly greater than for wipes taken prior to playing. There was no significant association between Pb or Mn in handwipes with traffic exposure. Dustfall accumulation was a significant predictor for Pb in the handwipes, and dust sweepings were a significant predictor of Mn in handwipes.  相似文献   

XANES analysis of the mechanisms of arsenic removal in biological iron and manganese treatment unit     

Yoko Fujikawa Daisuke Yoneda Atushi Minami Hiroshi Yashima Toshio Tonokai Sotoji Tani Masami Fukui Tatuhide Hamasaki Masataka Sugahara 《中国地球化学学报》2006,25(B08):113-113

Biological iron and manganese removal utilizing indigenous iron and manganese oxidizing bacteria （IRB hereafter） in groundwater can also be applied to arsenic removal according to our pilot-scale test. The arsenic removal probably occurred through sorption and complexation of arsenic to iron and manganese oxides formed by enzymic action of IRB. We investigated the chemical properties of iron and manganese oxides in IRB floc and the valence state of arsenic sorbed to the floc to clarify the mechanisms of the arsenic [especially As （Ⅲ）] removal. The floc samples were collected from two drinking water plants using IRB （Jyoyo and Yamatokoriyama, Japan）, and our pilot - scale test site where arsenic and iron removal using IRB is under way （Mukoh, Japan）. The Jyoyo and Yamatokoriyama IRB floc samples were subjected to As （Ⅲ） and As（Ⅴ） sorption experiments. The elemental composition of the floc samples was measured. XANES spectra were collected on As, Fe and Mn K-edges at synchrotron radiation facility Spring 8 （Hyogo, Japan）. FT-IR and the X-ray diffraction spectra of the samples were also obtained. The IRB floc contained ca. 35 % Fe, 0.3%-3.5% Mn and 2%-6% P. The samples were highly amorphous and contained ferrihidrites and hydrated iron phosphate. According to XANES analyses of IRB, As associated with IRB was in ＋5 valence state when As （Ⅲ） （or As （Ⅴ）） was added in laboratory sorption test, Fe in ＋3 valence state, and Mn a mixture of＋3 and ＋4 valence states. Small shift was observed in the XANES spectra of IRB on As K-edge as the equilibration time of the sorption experiment was increased. Gradual oxidation of a small amount of As （Ⅲ） associated with IRB or change in arsenic binding with sorption site were the probable mechanism.  相似文献