地质速率计—矿物氧扩散的应用     

傅斌  郑永飞 《地球科学进展》1997,12(5):428-433

概述了同位素封闭体系内的矿物氧扩散和同位素交换机制及其在地质速率计上的应用。火成岩从高温冷却或变质岩从高峰主质温度冷却过程中，由于冷却速度不同，扩散作用导致的矿物晶体内部及晶粒间氧同位素再平衡也有所不同。通过实测岩石中各组成矿物氧同位素比值，模式含量和颗粒半径，据矿物氧扩散和同位素交换模型，可以估算出岩石的冷却速率。  相似文献   

榴辉岩的化学分类   总被引：5，自引：0，他引：5       下载免费PDF全文

王式 《地质科学》1997,32(3):275-282

以山东荣成地区的榴辉岩为例,把榴辉岩分为镁一榴辉岩、铁一榴辉岩和钙一榴辉岩三类。三类榴辉岩的岩石化学,主要造岩矿物成分都有明显差别,石榴石分别是镁铝榴石、铁铝榴石和钙铝榴石。绿辉石的硬玉分子也有不同。三类榴辉岩的化学成分限制是Mg-榴辉岩MgO>10%,石榴石以镁铝榴分子占优势,Fe-榴辉岩的MgO<10,石榴石以铁铝榴石分子占优势。Ca-榴辉岩CaO>19%,石榴石以钙铝榴石分子优势。  相似文献   

试论矿产勘查中人的决定性因素     

贾大成 《吉林地质》1997,16(1):1-5

矿产勘查是一项系统工程，由多种因素构成，要想获得尽可能高的矿产勘查成果，仅依靠先进的成矿理论和找矿方法是不够的，还需注重掌握先进成矿理论与方法的管理人员的作用，在地勘行业调整与改革的现阶段，强调矿产勘查系统中人的决写性因素，认识人在矿产勘查中的地位与作用，提高勘查人员的素质，对调整，稳定发展地勘队伍具有一定的现实意义。  相似文献   

关于当前我国战略性矿产勘查工作几个问题的思考     

王瑞江 《地质通报》2004,23(11):1074-1077

战略性矿产勘查是近几年根据中国地勘管理体制的新变化和国家对矿产勘查工作的新要求提出的概念。本文从战略性矿产的基本内涵、战略性矿产资源勘查工作的性质与任务、战略性矿产资源勘查工作与传统矿产勘查工作的差异、战略性矿产资源勘查工作的管理体制与运行机制等几个方面进行了初步探讨，旨在明确其性质定位和目标任务，逐步建立国家出资的公益性地质工作与后续商业性矿产勘查工作良性互动、有机结合的有效机制，促进中国矿产勘查业全面、健康地发展。  相似文献   

内蒙古镁铁质-超镁铁质岩型铜镍矿床成矿条件与找矿远景分析   总被引：5，自引：2，他引：5  

刘国军  王建平 《地质与勘探》2004,40(1):17-20

按构造环境控岩控矿特点,划分区内铜镍型矿成矿(岩)带,分析成矿条件,研究了与该类矿床成矿有关的镁铁质岩、超镁铁质岩分布规律及铜镍硫化物成矿特征,提出了找矿方向和建议.  相似文献   

论江苏若干矿产资源开发利用的新方向     

尚培颖王浩  翁志华 《江苏地质》2004,28(3):183-187

江苏泥炭大多数为低有机质分解较强的低位泥炭，适于制作肥料或制成腐肥使用；江苏硅质原料丰富，一种以硅为主的化肥——硅肥正日益显示其重要性；湖泊淤泥具有颗粒微细、含砂量少、可塑性高、结合力强、干燥敏感性好和收缩率较大等特点，是生产空心砖的最佳原料；高家边组泥页岩和坟头组底部细粉砂质泥岩及泥质粉砂岩是良好的陶粒原料、砖瓦、陶瓷建材以及水泥用粘土质原料；利用矿泉水与茶的结合能够生产出高、中、低多效应的复合型新产品。上述尚未被利用或利用程度不够的矿产资源有着广泛的开发利用前景。  相似文献   

石岭沟-拐道沟铜-铅-锌多金属成矿带成矿地质条件分析     

常宗东  韦龙明  王设计  高卫宏  张万业 《矿产与地质》2004,18(2):122-127

成矿带位于北秦岭北部晚元古代-早古生代裂谷带南缘的变质火山岩区，受油房-皇台断裂的次级分支断裂及燕山-印支期的侵入岩体及次火山岩脉的联合控制，成矿地质条件与甘肃白银厂铜-铅-锌矿田相类似，成矿带内地表已发现多条铜-铅-锌矿(化蚀变)体，找矿潜力较大，只要进一步深入开展工作，有望找到与白银厂铜-铅-锌矿田相类似的大型一超大型铜-铅-锌多金属矿床。  相似文献   

云南白秧坪矿化集中区矿石矿物特征及银、钴赋存状态的初步研究   总被引：2，自引：0，他引：2  

陈开旭  何龙清  魏君奇  杨爱平  杨伟光  黄惠兰 《矿物学报》2004,24(1):61-67

云南白秧坪地区是以银、钴多金属矿化为特色的矿集区，成矿作用与兰坪盆地两侧的推覆构造系统密切相关，发育一套复杂的中低温热液矿物组合，出现了铜、钴、镍、铋等亲地幔元素的硫化物(硫钴镍矿、硫铋铜矿)，显示地幔深源物质可能参与了成矿作用。银、钴赋存状态的初步研究表明载银矿物主要为汞银矿、辉银矿、银黝铜矿、方铅矿、黝铜矿及砷、锑、铅硫盐矿物等，载钴矿物主要为硫钴镍矿、辉砷钴矿、含钴毒砂等硫化物。  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   

Chemical Composition of Ores from the Takara Volcanogenic Massive Sulfide Deposit, Central Japan     

Daigoro Yakushi  Mamoru Enjoji 《Resource Geology》2004,54(4):437-446

Abstract. The Takara volcanogenic massive sulfide (VMS) deposit occurs in Miocene formation of the Misaka Mountain, the South Fossa Magna region, central Japan. The tectonic setting of the Misaka Mountain is reconstructed to be a part of the paleo Izu-Ogasawara arc which collided with the Honshu arc and to form accreted body in the present position. The Takara deposit, therefore, is considered to have formed in the paleo Izu-Ogasawara arc.
The ores from the Takara deposit are classified into pyrite-type ore, chalcopyrite-type ore, and sphalerite-type ore on the basis of chemical composition and their mineral assemblages. Some pyrite-type ores are characterized by their high Au content. The Au content is hardly recognized in the chalcopyrite-type and sphalerite-type ores.
The ores from the Takara deposit have intermediate bulk chemical composition between those from the Besshi-type deposits and the Kuroko-type deposits that are two representative VMS deposits. However, the bulk chemical composition is closer to that from the Kuroko-type deposits. And moreover, chemical composition of tetrahedrite-tennantite series minerals (tetrahedrite) is similar to that from the Kuroko-type deposits. The bulk chemical composition (Cu, Zn, Co, Pb, and As contents) of ores is affected by the chemical composition of volcanic rocks associated with VMS deposits.  相似文献