黑龙江东安金矿潜火山岩的控矿作用   总被引：1，自引：0，他引：1  

郭继海  金凤鸣  汪长生 《矿产与地质》2004,18(3):232-235

东安金矿是黑龙江省发现的大型浅成低温热液低硫化物型金矿床。赋存于中生代潜流纹岩和晚印支期碱长花岗岩接触外带的断裂系统中，近矿围岩硅化强烈、冰长石化发育。通过对潜火山岩的控矿作用研究，认为该区钙碱性中酸性潜火山岩是成矿的重要条件。  相似文献   

黑龙江省东宁县洋灰洞子铜矿床成矿岩体特征   总被引：1，自引：0，他引：1  

王秀芝  赵清泉  董明全 《矿产与地质》2004,18(5):450-454

通过对洋灰洞子铜矿床的成矿岩体进行研究，进一步明确了其成矿地质背景，着重研究与铜钼矿床关系密切的花岗闪长岩体和花岗闪长斑岩体的岩性特征、岩石类型、岩石化学特点、成岩时代、物质来源及侵位方式等，确定了该区花岗闪长岩和花岗闪长斑岩为洋灰洞子斑岩型铜钼矿床的成矿母岩。  相似文献   

太白县大河滩铜-金-多金属矿点成矿条件及找矿前景分析   总被引：1，自引：0，他引：1  

李永勤  陈二虎  黄长青 《矿产与地质》2004,18(6):541-544

大河滩铜-金-多金属矿点处于两大板块碰撞对接带，其间有庞家河一马鞍桥近EW向铁-金矿带和斜峪关一二郎坝NE向铁-贵金属矿带通过，具有多次成矿作用叠加的特点，可与江西“银山式”大型铜-金多金属矿床的成矿条件、赋矿特征、成矿时代和矿化类型类比，具备形成大型矿床的成矿地质条件，找矿前景较大。  相似文献   

塔里木盆地西部古岩盐地质地球化学特征与成钾条件分析   总被引：11，自引：1，他引：11  

谭红兵  马海州  马万栋  董亚萍  张西营  许建新 《矿物岩石地球化学通报》2004,23(3):194-199

塔里木盆地是我国重要的成盐盆地,为我国最有远景的找古钾矿地区之一。本文通过多年野外实地调查和大量岩盐样品的化学分析,特别是岩盐中可以指示沉积阶段的Br×103/Cl系数等区域分布特征,联系前人研究资料,分别从构造环境、地层和岩相古地理、地球化学特征等方面进行了成钾条件分析。结果表明,莎车盆地西部喀什坳陷和库车盆地中部拜城坳陷宏观地质特征均有利于钾盐沉积;岩盐地球化学组成相对于正常海相沉积表现出明显的贫Br特征,属海陆交互相或海源陆相沉积。相比之下,莎车盆地的喀什次级坳陷是目前最有前景的找钾远景区。  相似文献   

安徽铜陵新桥铜-硫-铁-金矿床中石英闪长岩和辉绿岩锆石SHRIMP年代学及其意义   总被引：48，自引：3，他引：48       下载免费PDF全文

王彦斌刘敦一  蒙义峰曾普胜杨竹森  田世洪 《中国地质》2004,31(2):169-173

对安徽铜陵新桥铜-硫-铁-金矿床区内的石英闪长岩和辉绿岩中的锆石分别进行了SHRIMP精确定年研究,石英闪长岩中锆石206Pb/238U年龄为(140.4±2.2)Ma,辉绿岩中锆石的年龄较复杂,其中发现了元古代锆石颗粒,其锆石207Pb/206Pb年龄为(2261±14)Ma,(1612±8)Ma,(919±12)Ma,(831±17)Ma。另外还有一组早古生代年龄的锆石,锆石206Pb/238U年龄为(443±13)Ma。以上这些新资料说明该区可能存在元古代基底的信息,且燕山期岩浆活动对本区成矿具有重要意义。  相似文献   

疏降地下水引起地面塌陷浅析--以淮南煤矿区为例   总被引：4，自引：0，他引：4  

许光泉  沈慧珍 《中国地质灾害与防治学报》2004,15(4):64-68

以淮南西部矿区为例，介绍了该地区自20世纪60年代开采煤矿以来，由于疏降地下水，引起的地面塌陷。为了研究灰岩水动力场规律，先后在该区进行多时段、多水平放水试验。研究表明，覆盖粘土层、岩溶及人工疏降地下水，是该地区岩溶塌陷形成的基本条件。通过对粘土盖层性质、疏降地下水岩溶塌陷演化过程及塌陷机理与对应阶段过程综合分析，结合区域地质条件，掌握了塌陷点的分布规律。对目前西部地区塌陷“复活”、整治及未来城市规划，提出了建设性建议。  相似文献   

昆明白泥井3号隧道围岩稳定性FLAC3D模拟   总被引：4，自引：2，他引：4  

吴传斌  施斌  孙宇  赵永贵 《水文地质工程地质》2004,31(6):52-55

应用FLAC^3D数值模拟软件对昆明白泥井3号隧道围岩稳定性进行了分析和评价。结果表明隧道支护后围岩的最大变形出现在隧道右侧拱顶，为1．00cm；隧道支护后左侧拱和右侧拱脚处剪应变明显增大，为应力集中区；围岩可以通过自身应力、应变和能量的调整，使整个隧道围岩处于稳定状态；同时也表明FLAC^3D用于隧道围岩变形分析是可行的。  相似文献   

Improved Platinum-Group Element Extraction by NiS Fire Assay from Chromitite Ore Samples Using a Flux Containing Sodium Metaphosphate   总被引：1，自引：0，他引：1  

L. Paul Bédard  Sarah-Jane Barnes 《Geostandards and Geoanalytical Research》2004,28(2):311-316

Many chromite-rich rocks contain relatively high concentrations of the platinum-group elements (PGE). In many cases, the phases carrying PGE occur as either platinum-group minerals (PGM) or as base metal sulfides in solid solution in sulfides. In some cases, such as the UG-2 unit of the Bushveld Complex, the PGM are occluded inside chromite grains. Chromites are notably difficult to dissolve in most fluxes and if the chromite contains some PGM the possibility exists that not all the PGE will be recovered during fusion. In this work, shortcomings in published methods of analysis based on the nickel sulfide fire assay procedure were investigated and a new procedure developed based on the addition of sodium metaphosphate to the fusion mixture. Optimum composition of the fusion mixture was found to be 10 g sodium metaphosphate and 9 g silica to 10 g sample, 15 g sodium carbonate, 30 g lithium tetraborate, 7.5 g nickel and 4.5 g sulfur to achieve complete dissolution of chromite grains. The new flux mixture was evaluated by the analysis of reference material CHR-Pt+ (which is known to contain PGM inside chromite grains) and no undissolved chromite grains were found in the glassy slag. Analysis of the nickel sulfide beads from this fire assay using neutron activation analysis showed similar results for Rh and Ru when compared with published conventional true (or accepted) values, while Au, Ir, Os, Pd and Pt values determined here were 10 to 30% higher than the corresponding published conventional true values. It was concluded that the addition of sodium metaphosphate improved chromite dissolution in the flux and appears to improve PGE recovery.  相似文献   

Occurrence of Halogen-rich Phlogopite in Late Cenozoic Volcanic Rocks in the Japanese Arcs     

Akira Imai 《Resource Geology》2004,54(2):153-166

Abstract. Halogen-rich phlogopite occurs in the groundmass of andesite and dacite lavas from Late Tertiary to Quaternary volcanoes associated with native sulfur and limonite deposits (Shiretoko-Iwozan, Hachimantai, Adatara, Omeshidake, Masaki) and hydrothermal ore deposits (Harukayama, Muineyama, Hishikari) in Japan. The F contents of the halogen-rich phlogopite range from 3.6 to 5.7 wt%, corresponding to atomic F/(F+C1+OH) ratios ranging from 0.45 to 0.69. On the other hand, the Cl contents of the halogen-rich phlogopite are around 0.2 wt%. The atomic Mg/(Mg+Fe) ratios range from 0.69 to 0.83.
The fluorine intercept value [IV(F)] defined by Munoz (1984) of the phlogopites ranges from 0.79 to 3.17, and the chlorine intercept value [IV(Cl)] ranges from -7.11 to -7.77. The observed IV(F) of the phlogopites broadly overlap the range of the IV(F) for biotites from porphyry copper deposits. On the other hand, the observed IV(Cl) are significantly lower than the IV(Cl) for biotites from porphyry copper deposits. Whereas the F contents of the phlogopite appear more prominent compared to the Cl contents, the calculation of halogen intercept values revealed that the phlogopites are enriched in Cl with respect to the element distribution effect of Mg-Fe substitution. Since the degree of Cl enrichment of the phlogopite is more significant compared to that of biotite in porphyry copper deposits, the phlogopites are considered to have formed under the condition of significantly high activity of halogens. Hydrothermal ore deposits may be formed in magmatic hydrothermal system associated with volcanoes where halogen-rich phlogopite is formed by hypersaline fluid.  相似文献   

Oxidation of As-bearing gold ore—a comparison of batch and column experiments     

《Journal of Geochemical Exploration》2004,81(1-3):59-70

This study deals with the experimental determination of the rate of weathering and As release from Au-bearing sulfide ores of the Mokrsko-West deposit (Czech Republic). The elevated As contents in the ore and the possible As mobilisation must be taken into account due to the close proximity of the deposit to the Vltava River, a source of drinking water for Prague. Crushed and homogenized ore material was divided into four grain-size fractions showing uniform chemical and mineralogical composition and subjected to batch and column leaching experiments. The most important reactions controlling metal leaching include (i) oxidation of sulfides, (ii) carbonate equilibrium and (iii) precipitation of hydrated ferric oxides (HFO). Hydrated ferric oxides were found to be important sorbents of mobilized As. The highest concentration of As in the leachates was obtained from the 64–1000 μm fraction. The oxidation rate in the agitated batch experiment calculated on the basis of sulfate concentrations is an order of magnitude higher (3.8×10⁻⁹ to 4.4×10⁻⁸ mol SO₄²⁻ h⁻¹ g⁻¹) than in the static column experiment (9.6×10⁻¹⁰ to 7.4×10⁻⁹ mol SO₄²⁻ h⁻¹ g⁻¹). The higher oxidation rate of batch experiments is explained by abrasion of oxidation products (mainly HFO) and by further exposition of reaction surfaces of the sulfide grains.  相似文献