Metamorphism in Archaean greenstone belts: calculated fluid compositions and implications for gold mineralization

An inescapable consequence of the metamorphism of greenstone belt sequences is the release of a large volume of metamorphic fluid of low salinity with chemical characteristics controlled by the mineral assemblages involved in the devolatilization reactions. For mafic and ultramafic sequences, the composition of fluids released at upper greenschist to lower amphibolite facies conditions for the necessary relatively hot geotherm corresponds to those inferred for greenstone gold deposits (X_CO2= 0.2–0.3). This result follows from the calculation of mineral equilibria in the model system CaO–MgO–FeO–Al₂O₃–SiO₂–H₂O–CO₂, using a new, expanded, internally consistent dataset. Greenstone metamorphism cannot have involved much crustal over-thickening, because very shallow levels of greenstone belts are preserved. Such orogeny can be accounted for if compressive deformation of the crust is accompanied by thinning of the mantle lithosphere. In this case, the observed metamorphism, which was contemporaneous with deformation, is of the low-P high-T type. For this type of metamorphism, the metamorphic peak should have occurred earlier at deeper levels in the crust; i.e. the piezothermal array should be of the ‘deeper-earlier’type. However, at shallow crustal levels, the piezothermal array is likely to have been of ‘deeper-later’type, as a consequence of erosion. Thus, while the lower crust reached maximum temperatures, and partially melted to produce the observed granites, mid-crustal levels were releasing fluids prograde into shallow crustal levels that were already retrograde. We propose that these fluids are responsible for the gold mineralization. Thus, the contemporaneity of igneous activity and gold mineralization is a natural consequence of the thermal evolution, and does not mean that the mineralization has to be a consequence of igneous processes. Upward migration of metamorphic fluid, via appropriate structurally controlled pathways, will bring the fluid into contact with mineral assemblages that have equilibrated with a fluid with significantly lower X_CO2. These assemblages are therefore grossly out of equilibrium with the fluid. In the case of infiltrated metabasic rocks, intense carbonation and sulphidation is predicted. If, as seems reasonable, gold is mobilized by the fluid generated by devolatilization, then the combination of processes proposed, most of which are an inevitable consequence of the metamorphism, leads to the formation of greenstone gold deposits predominantly from metamorphic fluids.     

黄金的成色

黄金的成色并不是一成不变的，它成色的高低是与成矿温度、成矿阶段、深度、时代、变质程度、水溶液及风化作用等有一定关系，我们从这些关系中可以寻找到我们找矿的捷径和依据。     

湿法冶锰废渣中锰的形态分析与应用

将湿法冶锰废渣经过烘干、研细等预处理,按其所使用的原材料进行形态研究,通过筛选和实验,确定了废渣中的锰可用形态分析方法。在弄清废渣中锰的各种形态及含量的基础上,将其成果进行转化,用于指导工业生产、环境评价和废渣处理,具有很好的经济效益和社会效益。     

云南东川因民铜矿金矿化特征及成因初探

因民铜矿发育两种金矿化类型:一是铜矿的伴生金;二是热液构造蚀变岩型。化探样品分析结果显示,金矿化主要赋存于金箔箐断层上、下盘的角砾状蚀变岩内,空间上受岩性和断裂构造的双重控制。邻区拖布卡金矿的成矿地质背景与本区相似,在成矿地质年代上作以类比推测,认为喜马拉雅期是主成矿期。另外通过对光片镜下和化探原生晕样聚类分析研究,发现构造蚀变岩型金矿化具明显的多期多阶段性及热液特征。     

中国数字地质调查系统的基本构架 及其核心技术的实现

数字地质调查系统是贯穿整个地质矿产资源调查全过程的软件,涵盖地质矿产调查、矿产资源勘查、矿体模拟、品住估计、资源量估算、矿山开采系统优化等内容。考虑数字地质调查系统的应用技术层面,从数据“层”模型、数据流“池”技术、不同阶段数据模型继承技术、数据互操作技术等几个方面讨论了核心技术及其实现,通过基于无缝一体化技术的数据采集、管理、综合处理与成果表达,在实体或矿块的矿床建模技术与品住估计、储量估算等方面展现了全地质调查过程的数字化,不但为地质人员应用高新技术降低了门坎,而且极大地提高了研究精度和效率,丰富了成果的表现形式和服务形式。随着数字地质调查系统的完善和应用水平的提高,数字地质调查系统将成为中国地质调查的主流软件体系。     

鄂尔多斯盆地黄陵、东胜地区地温场对比

鄂尔多斯盆地黄陵、东胜铀矿区分别处于盆地南部渭北隆起的北侧边缘和盆地北部伊盟隆起的东部,赋矿层位都是中侏罗统直罗组。盆地南、北铀矿区在现今地温场及古地温场都存在明显差异,南部现今大地热值及热演化程度明显高于北部。对于下侏罗统延安组和石炭—二叠系煤层,黄陵地区镜质体反射率都高于东胜地区。通过镜质体反射率资料得出同一埋深的一套地层经历的最大古地温和对应的古地温梯度也有南部高于北部的现象。由于早白垩世后期盆地普遍整体抬升使得现今地温相对古地温降低,南部黄陵地区抬升剥蚀量大于北部东胜地区,导致古、今地温差异也大于后者。盆地南部庆阳—富县一带局部构造热运动,导致南部异常地温场的形成,使得南部热演化程度高于北部。     

大别地块东南缘逆冲滑脱构造体系及其对金矿的控制作用

大别地块自晚元古代以来主要经受了自北而南的推挤,并且发生了两次较强烈的南移运动,造成了地块前线逆冲滑脱构造体系。特别是中生代的推挤和滑移,不仅构造变形强烈,而且还伴有热事件,大别地块东南缘郯－庐断裂南延部分和广济－宿松平移－推覆型韧性剪切带均是＂热线构造＂,它们提供了深层次岩浆活动的通道。本区岩石以绿片岩－角闪岩相变质岩为主,含金背景值高,逆冲滑脱构造和韧性剪切带的活动与金元素的活化、迁移和富集创造了良好的条件。     

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

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.