乳砷铅铜石的发现与研究

乳砷铅铜石发现于1984年,在广西德保和平桂等矿区的硫化物型矿床的氧化带铁帽中.对该矿物的物理、化学和X射线粉晶分析、红外光谱分析以及差热分析等方面进行了测试研究,其结果与国外已知数据基本一致.矿物呈淡黄绿或深绿色,细粒状或葡萄状,硬度H=4,比重D=5.35,透明,二轴晶负光性,2V大,Ng=1.9817,Nm=1.9703,NP=1.9584.化学成分为PbO 35.19,CuO 30.64,As_2O_5 30.09,FeO 0.28,ZnO 0.05,H_2O 4.10(%).相应的化学分子式为Cu_(2.96)Pb_(1.21)(AsO_4)_(2.01)(OH)_(2.31)·0.59H_2O.X射线粉晶数据与JCPDS26～1410卡基本一政,衍射强线为3.14(10),3.24(8),2.92(8),2.55(8),2.74(7),2.49(7),2.27(7),4.51(6),4.94(5),2.66(4),1.902(4),1.817(4).计算的晶胞参数为a=10.236(?).b=5.904(?),C=14.213(?),β=106.39°,z=4,单斜晶系;空间群为A2/a.红外吸收光谱波数为3440、1640、870、820、775、465和1100、590、557(cm~(-1));差热分析吸收峰为580、773、812、889、898(℃).     

论金川硫化铜镍矿床中贵金属元素的分带机制

在金川硫化铜镍矿床最大的寓矿体内,贵金属元素存在明显分带:Pt、Pd、Au、Ag含量在边部较低,向中心部位逐渐增高;Os、Ir、Ru、Rh含量在中心部位较低,向边部逐渐增高。通过对实际资料的分析,认为这种分带特征是硫化物液相结晶分异作用造成的。     

瑞典硫化物矿山尾矿淋滤水的控制

在瑞典,硫化物矿尾矿污染水的淋滤造成巨大的环境污染问题。本文概述一项利用天然土覆盖尾矿、最大限度地减少淋滤水的调查报告。研究表明,天然土渗水性是如此之高,以致于起不到明显的隔水效果。天然土盖层只能减少高降雨量期或迅速化雪期的渗水量,而且只对淋滤水峰值有作用。但是,作为一种蓄水体,位于尾矿顶部的密封盖层具有重要意义,它可以增加蒸腾损失。     

中子活化分析在铼—锇法年龄测定中的应用

同位素稀释中子活化分析铼与感耦等离子体质谱法测定锇相结合，应用于辉钼矿及铜＿镍硫化物矿物的铼＿锇年龄测定，取得了满意的结果，扩大了铼＿锇测年法的应用范围。     

Origin of fluids in iron oxide–copper–gold deposits: constraints from δ 37Cl, 87Sr/86Sri and Cl/Br

The origin of the hypersaline fluids (magmatic or basinal brine?), associated with iron oxide (Cu–U–Au–REE) deposits, is controversial. We report the first chlorine and strontium isotope data combined with Cl/Br ratios of fluid inclusions from selected iron oxide–copper–gold (IOCG) deposits (Candelaria, Raúl–Condestable, Sossego), a deposit considered to represent a magmatic end member of the IOCG class of deposit (Gameleira), and a magnetite–apatite deposit (El Romeral) from South America. Our data indicate mixing of a high δ ³⁷Cl magmatic fluid with near 0‰ δ ³⁷Cl basinal brines in the Candelaria, Raúl–Condestable, and Sossego IOCG deposits and leaching of a few weight percent of evaporites by magmatic-hydrothermal (?) fluids at Gameleira and El Romeral. The Sr isotopic composition of the inclusion fluids of Candelaria, Raúl–Condestable, and El Romeral confirms the presence of a non-magmatic fluid component in these deposits. The heavy chlorine isotope signatures of fluids from the IOCG deposits (Candelaria, Raúl–Condestable, Sossego), reflecting the magmatic-hydrothermal component of these fluids, contrast with the near 0‰ δ ³⁷Cl values of porphyry copper fluids known from the literature. The heavy chlorine isotope compositions of fluids of the investigated IOCG deposits may indicate a prevailing mantle Cl component in contrast to porphyry copper fluids, an argument also supported by Os isotopes, or could result from differential Cl isotope fractionation processes (e.g. phase separation) in fluids of IOCG and porphyry Cu deposits.     

Hydrogen sulfide measurements in air by passive/diffusive samplers and high-frequency analyzer: A critical comparison

In this study, hydrogen sulfide (H₂S) measurements in air carried out using (a) passive/diffusive samplers (Radiello^® traps) and (b) a high-frequency (60 s) real-time analyzer (Thermo^® 450i) were compared in order to evaluate advantages and limitations of the two techniques. Four different sites in urban environments (Florence, Italy) and two volcanic areas characterized by intense degassing of H₂S-rich fluids (Campi Flegrei and Vulcano Island, Italy) were selected for such measurements. The concentrations of H₂S generally varied over 5 orders of magnitude (from 10⁻¹–10³ μg/m³), the H₂S values measured with the Radiello^® traps (H₂S_R) being significantly higher than the average values measured by the Thermo^® 450i during the trap exposure (H₂S_Ta), especially when H₂S was <30 μg/m³. To test the reproducibility of the Radiello^® traps, 8 passive/diffusive samplers were contemporaneously deployed within an 0.2 m² area in an H₂S-contaminated site at Mt. Amiata (Tuscany, Italy), revealing that the precision of the H₂S_R values was ±49%. This large uncertainty, whose cause was not recognizable, is to be added to that related to the environmental conditions (wind speed and direction, humidity, temperature), which are known to strongly affect passive measurements. The Thermo^® 450i analyzer measurements highlighted the occurrence of short-term temporal variations of the H₂S concentrations, with peak values (up to 5732 μg/m³) potentially harmful to the human health. The Radiello^® traps were not able to detect such temporal variability due to their large exposure time. The disagreement between the H₂S_R and H₂S_Ta values poses severe concerns for the selection of an appropriate methodological approach aimed to provide an accurate measurement of this highly toxic air pollutant in compliance with the WHO air quality guidelines. Although passive samplers may offer the opportunity to carry out low-cost preliminary surveys, the use of the high-frequency H₂S analyzer is preferred when an accurate assessment of air quality is required. In fact, the latter provides precise real-time measurements for a reliable estimation of the effective exposure to hazardous H₂S concentrations, giving insights into the mechanisms regulating the dispersion of this air pollutant in relation to the meteorological parameters.     

红旗岭3号含矿岩体地质年龄及其岩石学特征

以1号和7号岩体为代表的红旗岭铜镍硫化物矿床,是兴蒙造山带中典型的岩浆熔离型矿床。矿区内共有30多个镁铁-超镁铁质岩体,3号岩体是其中的含矿岩体,多年来因其地质产状与主要含矿岩体不同被认为形成于燕山期。本次工作对采自不同深度岩心样品中的单矿物角闪石进行⁴⁰Ar/³⁹Ar同位素年代学研究,得到（228.2±3.0 ）Ma的坪年龄和（230.1±7.1）Ma的等时线年龄。该年龄和近年发表的红旗岭1号岩体地质年龄基本一致,说明它们均为早印支期岩浆作用的产物。通过对比分析1号和7号主含矿岩体与3号岩体的岩石地球化学特征发现,无论是稀土元素还是微量元素图解均显示了它们具有相同的配分模式,暗示了这些岩体的同源性特点。     

胃肠酸度下中药及补铁制剂中铁活性的影响研究

在人体胃肠液的酸度条件下,采用正辛醇-水分配体系模拟药物在人体肠胃中的分配情况,研究了中药和补铁制剂中铁的形态及其在人体内的吸收情况,并探讨了中药不同比例的配伍、胃肠酸度及还原性物质的存在对水溶态铁和醇溶态铁的影响。结果表明,药物溶液中的铁形态与药物本身特性和配伍情况有关,酸度及配伍对药物中铁的溶出率和溶液中铁的形态有较大影响,人体对铁的吸收与胃肠酸度和还原性物质的存在有关。     

Phosphate removal from water by naturally occurring shale,sandstone, and laterite: The role of iron oxides and of soluble species

Aqueous phosphate removal by three geomaterials from Ivory Coast was evaluated to determine their potential application as low-cost phosphate adsorbents in wastewater treatment. Batch experiments showed that phosphate uptake strongly depended on pH. Laterite and sandstone dissolution was less pronounced compared to shale. A correlation between concentrations of aqueous cation species released from shale and phosphate uptake was observed. The kinetics were well described using the pseudo-second-order model. Isotherms displayed a saturation level on shale, while phosphate uptake continuously increased for laterite and sandstone. The removal efficiency decreased in the following ranking order: laterite > sandstone > shale. Laterite was also the most efficient adsorbent in column experiments. The high phosphate removal efficiency of laterite (8.3 mg PO₄ g^?1) was attributed to the presence of superparamagnetic low grain sizes of goethite. Laterite is a particularly promising material for further investigation in wastewater treatment technology such as constructed wetlands.