Usefulness of geological,mineralogical, chemical and chemometric analytical techniques in exploitation and profitability studies of iron mines and their associated elements

Due to the high number of variables involved in mine profitability studies, it is often very difficult to establish connections among them in order to provide a blend of market saleable quality products. In this sense, analytical chemistry together with chemometry are essential and indispensable disciplines to tackle these studies. The aim of this work was to demonstrate the utility of these disciplines to carry out optimization studies of iron mines. For this purpose, one of the most important iron mines of the Iberian Peninsula was chosen, sited in the mountain range of Sierra Menera, near the location of Ojos Negros (Teruel, Spain). Geological, mineralogical and chemical composition of 148 samples was analyzed, corresponding to different depths of three drill holes (named TE1, TE2 and TE3). In particular, aspects concerning to chemical composition are very important, since the mean contents of certain elements, such as phosphorus, sodium and potassium, should be restricted to the established limits to prevent that companies can drive back the raw material if they do not fulfil the necessary requirements. On the other hand, the large number of analysed samples drove us to use a statistical processing of the data. Among other aspects, it provides a way to find possible connections among a high number of variables and classify samples into compositional groups sharing similar composition, in order to limit the mineralised area and to obtain enough information about the amount of those chemical elements associated to iron ores. Data obtained from all these analytical techniques were in good agreement and provide a methodology that can be of wide interest applied to different geological studies.     

岩矿显微组构对水银洞金矿成因的指示

黔西南水银洞金矿为产于上二叠统龙潭组中的超大型、高品位金矿床,矿床由多个金矿体组成.工业金矿体顺层产于龙潭组含煤地层所夹的玄武质、硅质、生物碎屑碳酸盐岩中.对水银洞金矿赋矿地层岩石以及矿石显微组构进行了研究,矿石中主要载金矿物为细粒黄铁矿,具再生边、粒内孔隙、铸模孔隙结构及镶边生物矿化构造、铸模式生物矿化构造,是一典型的具沉积一成岩组构.金矿化与硅化有密切的成因联系,金与SiO2来源于峨嵋山玄武岩的喷溢活动,主要金矿体更多显示与峨嵋山玄武岩准同生特征.矿床为沉积一成岩弱改造成囚金矿床.     

东海黑潮区海水中磷酸盐的分布特征及成因探讨

本文报道了1987年夏、冬两个航次在26°50′～32°30′N,124°30′～131°30′E海区中可溶性无机磷酸盐的调查结果,阐明了磷的分布特征和形成机制。结果表明陆架区表层测值较高,大洋区为低值区,底层则相反。大洋水常年分层,中层水有爬坡涌升现象,其浓度与Aou呈正相关,与pH和S呈负相关。夏、冬两季底层磷与Aou呈正相关,其浓度变化主要依赖于生物过程。     

一种用磷酸钙法高效转染HEK 293T细胞方法的建立

利用磷酸钙转染法将lacZ-pShuttle质粒导入HEK 293T细胞中,实验证明,pH值、DNA纯度、转染后培养时间和甘油休克时间是影响转染效率的重要因素.转染后培养6h进行甘油休克效果最佳,比培养0h直接进行休克转染效率升高584.4%;甘油休克时间为4.5min时转染效果最佳,比不用甘油休克转染效率升高130.8%.通过对影响转染的几个条件进行优化,建立了1种可以高效转染HEK 293T细胞的方法,且简便易行.     

沉积物对磷酸盐的吸附与释放

本实验研究黄河口水文站沉积物对黄河水磷的吸附释放过程和东海１１１号站位沉积物对海水磷的吸附释放过程。并摸拟黄河沉积物在海水中磷的吸附释放过程。结果表明：底沉积物对磷的吸附相当迅速，无论是河泥还是海泥在２４ｈ内均能达到吸附平衡。吸附量与沉积物的量和水中原有磷的浓度有关，在不同的ｐＨ条件下，沉积物对磷的吸附是有显著差别的     

温和水热法制备MZr2(PO4)3(M=Na,K,Rb)

在温和的水热条件下分别制备出纯净的磷酸锆钠 [NaZr2 (PO4) 3 ]、磷酸锆钾 [KZr2 (PO4) 3 ]和磷酸锆铷 [RbZr2 (PO4) 3 ]。研究了原料配比、矿化剂 (氟离子 )、反应时间和温度等水热晶化条件对产物生成的影响。发现在较宽的温和水热条件下可以制得这三种磷酸锆盐 ;随着碱金属离子的增大 ,产物的生成条件越来越窄 ;最佳制备条件是 :F- ZrO2 =2、P2 O5 ZrO2 =3 (均为摩尔比 )、[ZrOCl2 ]=0 6mol L、反应温度 1 5 0℃、反应时间 2天。用水热法没有制备出同一系列磷酸锆盐中的磷酸锆锂 [LiZr2 (PO4) 3 ]和磷酸锆铯 [CsZr2 (PO4) 3 ]。采用XRD、SEM、IR、Raman和XPS等现代物化仪器对产物的结构与物相纯度进行了测定与表征     

Salt tolerance of Microcoleus vaginatus Gom., a cyanobacterium isolated from desert algal crust, was enhanced by exogenous carbohydrates

Microcoleus vaginatus isolated from a desert algal crust of Shapotou was cultured in BG-11 medium containing 0.2 mol l⁻¹ NaCl or 0.2 mol l⁻¹ NaCl plus 100 mg l⁻¹ sucrose, extracellular polymeric substances (EPS) or hot water-soluble polysaccharides (HWP), respectively. Photosynthetic oxygen evolution rates, photosystem II activity (Fv/Fm) and dark respiration of NaCl-stressed cells were enhanced significantly by the added sucrose or EPS under salt stress conditions (0.2 mol l⁻¹ NaCl). Compared with cells treated with salt alone, sodium contents in cells reduced significantly; the content of cellular total carbohydrate did not change, and intracellular sucrose, water-soluble sugar increased significantly following the addition of exogenous carbohydrates. Sucrose synthase (SS) activity of NaCl-stressed cells increased following the addition of sucrose, and sucrose phosphate synthase (SPS) activity of NaCl-stressed cells increased following the addition of exogenous sucrose, EPS or HWP compared with cells stressed with NaCl only. The results suggested that the extruded EPS might be re-absorbed by cells of M. vaginatus as carbon source, they could increase salt tolerance of M. vaginatus through the changes of carbohydrate metabolism and the selective uptake of sodium ions.     

义敦成矿带铜银铅锌锡矿产资源调查评价进展与潜力

义敦成矿带地处独特的大地构造部位，经历了复杂的地质构造演化和强烈的岩浆活动，成矿条件优越，矿产资源丰富。1999年实施国土资源地质大调查以来，相继发现了普朗、松诺、卓玛斑岩铜矿；砂西、热朗泽、夏隆等银铅锌矿；热隆、脚根玛锡矿；打马池觉铜金矿等一批具有重要找矿前景的矿床(点)。该地区矿产资源勘查工作程度低，蕴藏着较大的找矿潜力，有望成为国家级重要的有色及贵金属矿产勘查和开发基地。     

加强富锰矿勘查工作,促进锰业发展

我国现有锰矿资源状况，不能满足钢铁工业发展的需要。寻找低磷低铁低硅富锰矿，是解决锰矿资源短缺的重要途径。城口锰矿具有较大的找矿前景，锰矿层产出稳定，锰含量高，铁含量低，烧失量大。加强城口矿区勘查，扩大矿床规模，可望成为我国锰矿的重要生产基地。     

Feasibility and cost of creating an iron-phosphate coating on pyrrhotite to prevent oxidation

 Acid mine drainage (AMD) occurs when sulfide minerals are exposed to an oxidizing environment. Most of the methods for preventing AMD are either short-term or high cost solutions. Coating with iron phosphate is a new technology for the abatement of AMD. It involves treating the sulfide with a coating solution composed of H₂O₂, KH₂PO₄, and sodium acetate as a buffer agent. The H₂O₂ oxidizes the sulfide surface and produces Fe³⁺ so that iron phosphate precipitates as a coating on the sulfide surface. Experiments performed under laboratory conditions prove that an iron phosphate coating can be established on pyrrhotite surfaces with optimal concentrations of the coating solution in the range of: 0.2M/0.01M H₂O₂, 0.2M KH₂PO₄, and 0.2M sodium acetate NaAc, depending on the experimental scale. Iron phosphate coating may be a long-term solution to the problem of AMD. The method would be easy to implement; the reagent cost, however, is not low enough, although it is lower than the conventional treatment with lime. Received: 30 March 1995 · Accepted: 6 September 1995