山西铝土矿床成矿物质来源     

卢静文  彭晓蕾  徐丽杰 《吉林大学学报(地球科学版)》1997,(2)

山西铝土矿矿石中鲕、豆、碎屑等组构均具红土性质，结合化学成分特征、稀土元素特征、氧同住素特征、锆石等副矿物特征及含矿岩系底部岩层与下伏中奥陶纪灰岩关系和矿床分布与古陆、古岛的依赖关系等方面分析，铝土矿的成矿物质多是异源的，多为古陆上的铝硅酸盐岩红土风化产物，经流水以机械碎屑形式被搬运至海盆，沉积成矿  相似文献   

关于侵入岩体中金矿床成因研究若干问题的讨论   总被引：9，自引：1，他引：9  

莫测辉  王秀璋 《地质论评》1997,43(2):139-147

各时代、不同类型侵入岩中的金矿床是金矿的主要类型。关于金矿床与岩体的成因关系目前尚存在不同的看法，但传统的岩浆热液成因观点仍居统治地位，其原因往往在于不少研究者把岩液热液成因当成了固定模式应用于具体矿床的研究，而不是建立在综合研究的基础之上。本文结合近年来金矿的研究进展，强调侵入岩中金矿床的研究的研究要综合考虑成岩成矿的时代与时差，成矿流体和成矿物质的来源等各方面因素。金矿床定年的进展研究表明，矿  相似文献   

关于银山矿床成矿作用的几个问题——兼与《江西银山铜铅锌金银矿床》的作者商榷     

张德会 《地质论评》1997,43(5):490-497

银山多金属矿床是一个特大型火山—潜火山热液矿床,具有复杂的多期多阶段的成矿作用和有序的成矿分带。成矿作用主要为火山—潜火山热液作用,但在此之前,还经历了一期由韧脆性剪切带形成而引起的动力变质热液作用。根据矿体与3个旋回潜火山岩体的时空关系,火山—潜火山热液成矿作用又可分为两个成矿期和5个成矿阶段。矿床地质地球化学研究表明成矿作用在空间上具有定向迁移的特点,结合流体动力学计算机数值模拟认为定向迁移的根本原因是构造岩浆脉动和隐伏岩体形态产状。笔者认为,矿区深部可能有隐伏岩体,但对隐伏的斑岩铜矿床不应抱很大希望  相似文献   

内蒙古铜矿床区域成矿特征初步研究   总被引：3，自引：3，他引：3  

沈存利  苏宏伟  王守光 《西北地质》2004,37(3):43-50

近年来，随着内蒙古周边地区铜矿的地质找矿不断取得重大突破，以及内蒙古铜矿勘查取得的一系列重要新进展，在内蒙古开展铜矿地质勘查工作已引起国内外地质学家的关注。笔者经综合研究地质构造、铜矿勘查及有关地球化学等新信息后，均显示出巨大的铜矿找矿潜力。从内蒙古自治区铜矿勘查史以及与邻区对比研究人手，研究总结了全区铜矿床及铜异常空间分布特征，划分出3个铜成矿区(带)，并进一步划分出铜矿床或异常密集区，初步提出了寻找大型及超大型铜矿床的找矿方向。  相似文献   

广西新型矿物材料发展方向初探     

李艺 《矿产与地质》2004,18(1):42-45

新材料是发展高新技术产业的基础。根据广西的矿产资源优势和在矿物材料方面的研究基础和技术力量，提出了加强工艺矿物学研究，大力发展广西新型矿物材料的研究开发方向，特别提出了超细改性矿物粉体材料、环保矿物材料、节能保温矿物材料、高技术陶瓷材料和合成矿物晶体材料等材料体系中的重点开发方向。  相似文献   

云南会泽超大型铅锌矿床成因研究中的几个问题   总被引：6，自引：0，他引：6  

黄智龙  李文博  张振亮  韩润生  陈进 《矿物学报》2004,24(2):105-111

位于川-滇-黔铅锌多金属成矿域中南部云南会泽超大型铅锌矿床可能是一种新的铅锌矿床类型，该类铅锌矿床明显特征是规模大、品位富、伴生有用元素多，暗示其成矿环境较为特殊。从成矿时代、成矿物质来源、成矿流体来源与演化，以及峨眉山玄武岩与成矿的关系等方面分析了会泽超大型铅锌矿床的研究进展及国内外研究现状，认为矿床成矿时代与西南大面积峨眉山玄武岩成矿时代相近，成矿物质和成矿流体具有“多源性”，成矿流体存在均一化过程，区域大规模流体运移在该区铅锌成矿过程中具有重要意义，峨眉山玄武岩岩浆活动与铅锌成矿具有密切的成因联系，矿床可能为“均一化成矿流体贯入成矿”的产物。  相似文献   

Analysis of Sediments and Soils by X-Ray Fluorescence Spectrometry Using Matrix Corrections Based on Fundamental Parameters   总被引：2，自引：0，他引：2  

Jacinta Enzweiler  Maria Aparecida Vendemiatto 《Geostandards and Geoanalytical Research》2004,28(1):103-112

Wavelength dispersive X-ray fluorescence spectrometry (WD-XRF) is widely used for the analysis of soils and sediments using well characterised procedures. However, difficulties can occur with samples such as unknowns containing small amounts of ore materials and samples collected from contaminated sites where trace elemental concentrations can exceed the concentration range for routine analysis. We studied the performance of a commercially available method, based on fundamental parameters (FP) to correct matrix effects. The spectrometer was originally calibrated with elemental or simple compound calibrants. Samples were analysed as pressed powder pellets. Eighteen sediment and soil reference materials, three of them with certified values for some of their constituents, were used to evaluate accuracy, by comparing results with recommended values and their standard deviations (RV ± 2s) or certified values and their confidence intervals (CV ± Cl). When results fell systematically outside these intervals, calibrations were refined with geochemical reference materials. The best agreement of results with recommended and certified values was obtained when the contents of H₂O and C in each sample were included as matrix constituents during calculations. The detection limits of trace elements tended to be relatively high, because the measuring conditions employed were not maximised for sensitivity. The main advantage of the method tested was that it enabled the analysis of samples with high concentrations of trace elements and the determination of elements such as F, Bi, Sb and W, which are not commonly included in quantitative XRF analysis of geological samples.  相似文献   

A Reflection on Mg, Cd, Ca, Li and Si Isotopic Measurements and Related Reference Materials   总被引：6，自引：1，他引：6  

Jean Carignan  Damien Cardinal  Anton Eisenhauer  Albert Galy  Mark Rehkamper  Frank Wombacher  Nathalie Vigier 《Geostandards and Geoanalytical Research》2004,28(1):139-148

This contribution aims to report the reflections we had with the scientific community during two international workshops on reference materials for stable isotopes in Davos (2002) and Nice (2003). After evaluating the isotopic homogeneity of some existing reference materials, based on either certificates, literature data or specific inter-laboratory rounds, we confirm these as primary reference materials or propose new ones relative to which stable isotope compositions should be reported. We propose DSM-3 for Mg, NIST SRM 915a for Ca, L-SVEC for Li and NBS28 for Si. Cadmium does not yet have a well identified delta zero material, although three commercial mono-elemental Cd solutions have yielded the same isotopic composition relative to one another. In order to scale the linearity of any mass spectrometer, some secondary reference materials are also proposed: Cambridge-1 solution for Mg, the "Münster-Cd" and JEPPIM Cd solutions for Cd and the "Big Batch" silicate for Si. The team from Nancy propose to prepare a mixed spike solution for Li isotopes. Well-characterised natural samples such as ocean or continental waters, diatoms, sponges, rocks and minerals are needed to validate the entire analytical procedure, particularly to take into account the effect of sample mineralisation and of chemical manipulations for elemental separation prior to analysis.  相似文献   

Precise/ Small Sample Size Determinations of Lithium Isotopic Compositions of Geological Reference Materials and Modern Seawater by MC-ICP-MS   总被引：6，自引：1，他引：6  

Alistair B. Jeffcoate  Tim Elliott  Alex Thomas  Claudia Bouman 《Geostandards and Geoanalytical Research》2004,28(1):161-172

The Li isotope ratios of four international rock reference materials, USGS BHVO-2, GSJ JB-2, JG-2, JA-1 and modern seawater (Mediterranean, Pacific and North Atlantic) were determined using multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). These reference materials of natural samples were chosen to span a considerable range in Li isotope ratios and cover several different matrices in order to provide a useful benchmark for future studies. Our new analytical technique achieves significantly higher precision and reproducibility (< ± O.3%o 2s) than previous methods, with the additional advantage of requiring very low sample masses of ca . 2 ng of Li.  相似文献   

Geochemistry of ore-forming fluids and geological significance of the Kuoerzhenkuola gold field in Xinjiang, China     

SHEN Ping  SHEN Yuanchao  LIU Tiebing  LI Guangming & ZENG Qingdong Institute of Geology  Geophysics  Chinese Academy of Sciences  Beijing  China 《中国科学D辑(英文版)》2005,48(11)

The Kuoerzhenkuola gold field (including the Kuo- erzhenkuola and the Buerkesidai gold deposits), lo- cated 68 km east of Jimunai County in northern Xing- jiang, China, is an important component of the Sawuer gold belt which is the eastward extending part of the Zarma-Sawur gold-copper belt in Kazakhstan. Some studies are concerned with the geology of the gold ores[1―3], the associated volcanic rocks[4], radiogenic isotope[5―8], and the ore-forming environment[8]. Most researchers inferr…  相似文献