The solubility of iron sulphides in synthetic and natural waters at ambient temperature

A critical evaluation of literature values for the solubility products, K _sp ^NBS = [Fe²⁺][HS^–] Fe²⁺ HS^– (H _NBS ⁺ )^–1, of various iron sulphide phases results in consensus values for the pKs of 2.95 ± 0.1 for amorphous ferrous sulphide, 3.6 ± 0.2 for mackinawite, 4.4 ± 0.1 for greigite, 5.1 ± 0.1 for pyrrhotite, 5.25 ± 0.2 for troilite and 16.4 ± 1.2 for pyrite.Where the analogous ion activity products have been measured in anoxic freshwaters in which there is evidence for the presence of solid phase FeS, the values lie within the range of 2.6–3.22, indicating that amorphous iron sulphide is the controlling phase. The single value for a groundwater of 2.65 (2.98 considering carbonate complexation) agrees. In seawater four values range between 3.85 to 4.2, indicating that mackinawite or greigite may be the controlling phase. The single low value of 2.94 is in a situation where particularly high fluxes of Fe (II) and S (–II) may result in the preferential precipitation of amorphous iron sulphide. Formation of framboidal pyrite in these sulphidic environments may occur in micro-niches and does not appear to influence bulk concentrations. Calculations show that the formation of Fe₂S₂ species probably accounts for very little of the iron or sulphide in most natural waters. Previously reported stability constants for the formation of Fe (HS)₂ and (Fe (HS)₃)^– are shown to be suspect, and these species are also thought to be negligible in natural waters. In completely anoxic pore waters polysulphides also have a negligible effect on speciation, but in tidal sediments they may reach appreciable concentrations and lead to the direct formation of pyrite. Concentrations of iron and sulphide in pore waters can be controlled by the more soluble iron sulphide phase. The change in the IAP with depth within the sediment may reflect ageing of the solid phase or a greater flux of Fe (II) and S (–II) nearer the sediment surface. This possible kinetic influence on the value of IAPs has implications for their use in geochemical studies involving phase formation.     

Brine-pool deposition for the Zn–Pb–Cu massive sulphide deposits of the Bathurst mining camp, New Brunswick, Canada. II. Ocean anoxia during mineralisation

Current models of massive sulphide ore genesis in the Bathurst mining camp, New Brunswick, involve settling of sulphide particles from a stagnating, low-salinity hydrothermal plume spreading laterally in an anoxic ocean layer with minimal sulphate content. There is fragmentary evidence of ocean anoxia in the form of local fine lamination in the shales that host some of the deposits but the total organic carbon, S, Fe, U/Th, Ni/Co, V/Ni and V/Cr relationships indicate deposition under oxic or dysoxic conditions. Vanadium and Mn values range from oxic to anoxic and sulphate-reducing to non-sulphate reducing but Mn may be anomalously low due to derivation by erosion of acidic volcanic rocks. The somewhat equivocal physical and chemical data, combined with the likely disturbing effects of penecontemporaneous volcanism, considerably weaken the case for an anoxic bottom layer in a static ocean. The presence of barite with ambient seawater ³⁴S values in Brunswick no. 12 ore, and the abundance of sulphate in modern euxinic basin waters, make a sulphate-free layer unlikely, even if anoxic. Sulphate-bearing, low-salinity fluids mixing with seawater would lead to growth of barite-bearing chimneys and baritic rubble mounds, which are not observed. A model involving brine-pool deposition better explains the major features of the Bathurst ores.     

中国开辟区不利开采地形类型及其分布

利用1998年"大洋一号"调查船近海底作业所获的深拖海底电视和照相系统资料,对中国开辟区不利开采地形类型及其分布特征进行了研究,并对海底地形的坡度进行了计算,结果表明:(1)中国开辟区东、西两区海底的东向坡和西向坡是均衡分布的。东、西两区海底地形坡度的分布特征明显不同,东区海底地形坡度以0～15°为主,而西区坡度大于3°的地形则很少。坡度大于5°的地形主要分布于坡脚处,特别是坡度超过15°的地形总是出现在水深变化的转折点处。(2)研究区不利开采地形可分为坡度为5～15°和大于15°两种类型,东区地形坡度大于5°的不利开采地形比西区多14%,东区坡度大于15°的地形为3.6%,比西区(仅为1.4%)多,东、西两区都有少量坡度近90°的地形出现,并且这种地形在东区所占比率比西区大,说明东区断崖、陡坎和断裂沟槽比西区多,地形也更为复杂多变。     

南海尖峰海山多金属结壳地球化学

南海尖峰海山多金属结壳富含30多种元素,其锰铁矿物主要由钡镁锰矿,δ-MnO_2和FeOOH·xH_2O组成。与其它海区的结壳相比,尖峰海山结壳富含Cu、Ni、Ba、Zn、Pb等元素,而Co、Ti、稀土元素(REE)、Sr等元素相对较贫。研究表明,HREE亏损,具明显的Ce正异常,较明显的Tb正异常和Yb负异常。这是氧化弱碱性海洋环境所致。结壳是水成作用的产物,它的形成受南海独特的古海洋环境所控制,海底火山热液作用,可能也是影响因素之一。     

地形坡度对多金属结核分布的控制作用

选取我国东太平洋多金属结核开辟区内的一个区域作为研究区,利用人工神经网络中应用最为广泛的BP网络,建立控制多金属结核分布的地质因素与多金属结核分布之间的映射关系,探讨地形坡度对多金属结核分布的控制作用.结果表明,在经度、纬度、水深、坡度四个因素中,坡度对结核分布影响程度最大;多金属结核主要分布于坡度小于5°的地方;当坡度小于5°时,丰度与地形坡度呈正相关,品位与地形坡度呈负相关,丰度与品位呈负相关;品位与坡度似呈指数关系,坡度增大,品位降低.     

东太平洋多金属结核分布的二维趋势面分析

对规则网的 469个测站的多金属结核丰度和 93个测站的 Mn、 Cu、 Co、 Ni元素进行趋势面分析 ,经 F检验 ,各变量的变异性显著 ,拟合度较低 ,表明多金属结核丰度及 Mn、Cu、Co、Ni金属元素的控制因素比较复杂。趋势面分析结果与相关分析结果一致 ,Mn、Cu、Ni元素有极相似的趋势特征 ,有两个轴向分布 ,一个为东西向轴 ,高值区在东部 ,另一个为北西向轴 ,高值区在北西部 ;结核丰度与 Co也有极相似的趋势特征 ,高值区在西部。应用逐次趋势面分析的结果将结核丰度的地质特征分解成各种简单控制因素的叠加 ,使对多金属结核的控矿因素、分布规律和物质来源的研究方法多样化     

豫西太山庙花岗岩体特征与多金属矿产的关系

经从岩石学、矿物学、地球化学等方面对燕山期太山庙花岗岩体详细研究,认为该岩体侵入为一重要构造热事件,控制着区内多个多金属矿床的形成与规模。本文着重探讨和阐述太山庙花岗岩体特征及其对周边矿床的控矿关系。     

Information structure analysis for quantitative assessment of mineral resources and the discovery of a silver deposit

We propose an information-structure-analysis (ISA) method to quantify the correlations between quantitative and qualitative variables as well as within each type of variable. This method is applied to the evaluation of mineral resources in the western Zheijiang Province of China. The district contains a number of silver-bearing Fe–Cu–Pb–Zn mineral deposits near igneous complexes and FeCuPbZn zones away from the complexes. Silver anomalies occur not only in the known Fe–Cu–Zn–Pb deposits, but also in the country rock, suggesting the possible existence of silver deposits far from the igneous complexes.The tonnage distribution of silver is modeled by Monte Carlo simulation. This simulation is conducted on the basis of the correlations between silver (Ag) and lead (Pb), since no known data on silver is available. The known tonnage distribution of lead in 11 control cells was used to approximate the tonnage distribution of silver in the Monte Carlo simulation. With ISA and Monte Carlo methods, the total amount of potential polymetallic resources in 49 cells in the western Zhejiang Provice is predicted. Significantly, a deposit with about 24 tonnes of silver has been found within our exploration target area.     

Petrology, geochemistry and the mechanisms determining the distribution of platinum-group element and base metal sulphide mineralisation in the Platreef at Overysel, northern Bushveld Complex, South Africa

Platinum-group element (PGE) mineralisation within the Platreef at Overysel is controlled by the presence of base metal sulphides (BMS). The floor rocks at Overysel are Archean basement gneisses, and unlike other localities along the strike of the Platreef where the floor is comprised of Transvaal Supergroup sediments, the intimate PGE–BMS relationship holds strong into the footwall rocks. Decoupling of PGE from BMS is rare and the BMS and platinum-group mineral assemblages in the Platreef and the footwall are almost identical. There is minimal overprinting by hydrothermal fluids; therefore, the mineralisation style present at Overysel may represent the most ‘primary’ style of Platreef mineralisation preserved anywhere along the strike. Chondrite-normalised PGE profiles reveal a progressive fractionation of the PGE with depth into the footwall, with Ir, Ru and Rh dramatically depleted with depth compared to Pt, Pd and Au. This feature is not observed at Sandsloot and Zwartfontein, to the south of Overysel, where the footwall rocks are carbonates. There is evidence from rare earth element abundances and the amount of interstitial quartz towards the base of the Platreef pyroxenites that contamination by a felsic melt derived from partial melting of the gneissic footwall has taken place. Textural evidence in the gneisses suggests that a sulphide liquid percolated down into the footwall through a permeable, inter-granular network that was produced by partial melting around grain boundaries in the gneisses that was induced by the intrusion of the Platreef magma. PGE were originally concentrated within a sulphide liquid in the Platreef magma, and the crystallisation of monosulphide solid solution from the sulphide liquid removed the majority of the IPGE and Rh from it whilst still within the mafic Platreef. Transport of PGE into the gneisses, via downward migration of the residual sulphide liquid, fractionated out the remaining IPGE and Rh in the upper parts of the gneisses leaving a ‘slick’ of disseminated sulphides in the gneiss, with the residual liquid becoming progressively more depleted in these elements relative to Pt, Pd and Au. Highly sulphide-rich zones with massive sulphides formed where ponding of the sulphide liquid occurred due to permeability contrasts in the footwall. This study highlights the fact that there is a fundamental floor rock control on the mechanism of distribution of PGE from the Platreef into the footwall rocks. Where the floor rocks are sediments, fluid activity related to metamorphism, assimilation and later serpentinisation has decoupled PGE from BMS in places, and transport of PGE into the footwall is via hydrothermal fluids. In contrast, where the floor is comprised of anhydrous gneiss, such as at Overysel, there is limited fluid activity and PGE behaviour is controlled by the behaviour of sulphide liquids, producing an intimate PGE–BMS association. Xenoliths and irregular bands of chromitite within the Platreef are described in detail for the first time. These are rich in the IPGE and Rh, and evidence from laurite inclusions indicates they must have crystallised from a PGE-saturated magma. The disturbed and xenolithic nature of the chromitites would suggest they are rip-up clasts, either disturbed by later pulses of Platreef magma in a multi-phase emplacement or transported into the Platreef from a pre-existing source in a deeper staging chamber or conduit.     

陈家杖子金矿地球化学特征及其指示意义

陈家杖子金矿是通过1∶5万化探工作发现的斑岩型金多金属矿, 其地球化学异常特征可作为在该区寻找类似矿床标志。该矿东部还有形成多金属矿的潜力。在此类土壤覆盖区应采用土壤测量。该金矿的发现反映了在我国中西部地区利用常规方法来发现新矿床的巨大潜力。