Flotation of oxidized minerals of copper using a new synthetic chelating reagent as collector

A new synthetic reagent containing a mixed aliphatic-aromatic structure, with a hydrocarbon chain and an aminothiophenol chelating group, has proven to be an effective collector for the flotation of chrysocolla minerals. The flotation is optimum in the narrow pH range of 5.5 to 6, falls sharply at pH 5, and is moderate in the pH range 7 to 11. Infrared spectra indicate that copper aminothiophenolate chelates are formed on the surface of the chrysocolla under the conditions of maximum flotation.     

南平花岗伟晶岩中铯沸石的研究

目前在中国已发现两种铯矿物，即南平石和铯沸石，其中铯沸石主要分布在新疆、陕西、河南省的花岗伟晶岩中，在华南，南平花岗伟晶岩是迄今所报道的铯沸石的唯一产地。我们将南平钩沸石分成原生和次生两类，本文详细报道了南平铯沸石的产状、物性和光性、化学成分、Ｘ射线衍射特征、红外光谱、差热分析和形成过程。     

超高压变质岩矿物中的显微构造缺陷:来自TEM和FTIR研究的证据

超高压变质矿物的某些显微构造缺陷可能指示了岩石短暂和快速抬升过程。文中报道了中国大别山双河地区超高压硬玉石英岩矿物显微构造缺陷的透射电镜(TEM)和Fourier变换红外光谱(FTIR)的研究结果。用TEM研究方法,在硬玉石英岩中硬玉包裹体内发现了亚微米级天然蒙钠长石(MA,C2/m)、高钠长石(HA,C)和低钠长石(LA,C)三种多形变体。表明岩石在折返过程经历过高温变质作用(>930℃),以及退变质过程的快速冷却;在石英包裹体内发现了纳米级柯石英和石盐子矿物,提供了柯石英转变为石英以及峰期变质条件下高盐流体存在的证据。"名义上无水矿物"(NAMs)的结构水(OH/H2O)是以缺陷形式赋存于矿物结构中。FTIR分析结果显示硬玉、石榴石、金红石和石英中结构水的平均含量分别为1000×10-6、(900~1600)×10-6、>2000×10-6和<4×10-6,硬玉石英岩全岩含水量为(490~600)×10-6,表明在高压-超高压变质作用过程中,地壳或原岩中的水可以通过这些NAMs携带到地球深部。该类显微构造缺陷可能是大陆碰撞造山带在高应变速率下的局部弱化和深部断层作用的结果。     

赤柏松No.1含镍基性岩体中矿物界生(Synantectic)现象浅析

在两种相邻矿物边界上生长出第三种矿物的现象称为界生。界生现象在长白山区赤柏松镍矿田诸含镍基性辉长苏长岩岩体中广泛发育。通过研究,作者提出界生现象的多种成因观点,并在矿物学、矿物化学与热力学研究的基础上把界生现象区分为原生与次生两大类。研究不同成因的界生现象可提供大量地质成因信息,用手成岩成矿作用的研究。     

利用电子探针研究甘肃陇南赵家庄金矿载金矿物特征

应用偏光显微镜与电子探针相结合的手段是研究载金矿物的主要方法。本文采用镜下鉴定和电子探针分析技术,对赵家庄金矿中载金矿物含量、形态特征及其与其他矿物的空间关系开展研究,并对载金矿物进行定性和定量分析,探寻具有找矿意义的载金矿物和总结标志矿物特征。结果表明:研究区金矿石中主要载金矿物为黄铁矿,少量为黄铜矿、闪锌矿,这些载金矿物中Au含量依次为:细晶黄铁矿粗晶黄铁矿草莓状黄铁矿黄铜矿。不同时期的黄铁矿(粗晶黄铁矿、细晶黄铁矿、草莓状黄铁矿)中Au的分布均匀,但存在差异性,主要表现为细晶黄铁矿和草莓状黄铁矿中的Au含量较高(平均含量0. 14%～0. 18%),这种现象表明此类矿物为构造热液期形成,金易富集。Au以两种形式存在,一种是"可见金"包裹于脉石矿物中,或以裂隙金的形式嵌布在矿物晶隙及裂隙中;另一种是"不可见金"以纳米级颗粒金的形式存在于载金矿物中,也是Au的主要存在形式。本研究为后期矿床的成因、成矿过程和成矿机理研究提供了佐证,同时易于根据含金矿物的特征选择合适的选冶方法。     

印尼古邦岛(KUPANG)卡菲默纳努(KEFAMENANU)千岛矿区 锰矿地质特征及成因探讨

印尼千岛锰矿贮存于白垩系上统砂岩、泥岩中,呈层状、似层状产出,具有层控特征,局部遭受断裂构造破坏。通过对矿区成矿地质条件分析,初步认为矿床属于海相碎屑沉积类型锰矿床,具有较好的找矿远景。     

河套地区土壤矿物组成分析及与各元素的关系

通过对河套地区土壤中矿物组成的分析研究,土壤中矿物组成中砂质成分主要为石英、长石、方解石,黏土矿物组合主要为伊利石、绿泥石和高岭石,此外还有角闪石等少量矿物成分。在砂土、粉砂土中石英、长石含量较高,在黏土质为主的土壤中黏土矿物含量增加。黏土矿物与石英以及长石呈负相关关系,与大多数元素呈明显正相关关系,黏土矿物对各元素具有明显吸附性;石英、长石与各元素含量呈负相关关系,说明其对元素不具有吸附性。     

The composition and age of the Argillite Sequence (sedimentary cover of the continental slope, Sea of Japan)

The Argillite Sequence located at the base of the sedimentary cover on the continental slope of the Sea of Japan was studied by petrographic, palynological, and X-ray diffraction methods. Two spores-pollen complexes were distinguished in it: the Late Oligocene reflecting cooling and the Early Miocene corresponding to initiated warming. The data obtained indicate that the sequence is composed of terrigenous silty-clayey sediments that accumulated in shallow coastal-marine settings. The global sea-level rise at the Early-Middle Miocene transition, combined with the regional tectonic processes, determined the basin deepening, owing to which the argillite sequence was overlain by thick Middle Miocene diatomaceous-clayey sediments. Due to tectonic movement along existing faults in the terminal Late Miocene, the argillite sequence occurring initially at depths of at least 400–500 m was locally exhumed to the basin bottom.     

Characterization of an Area Polluted by Copper and Zinc:the Relation between Soil Texture,Mineralogy and Pollutant Concentration

Abstract: Twenty-four soil samples were collected at three depths from an approximately 2.5 acre contaminated site in southern Piedmont (Italy) and then analyzed. The main soil parameters determined were: pH, Cation Exchange Capacity (CEC), particle size distribution, total organic carbon (TOC) content and retained metal concentration. The mineral phases were identified by X-Ray Powder Diffraction (XRPD). All of the samples contained Zn and Cu resulting from industrial contamination during the last century, and those obtained at depths of 20-40 cm consistently showed the highest levels. To determine which size fraction was most active in the retention process, the samples were separated into four fractions (≤2 mm, ≤63 μm, ≤30 μm and ≤2 μm) and the amount of pollutant measured in each. It was found that metal retention was the highest in the clayey fraction, whose clay minerals were identified by XRPD after K+ and Mg2+ saturation, glycerol treatment and heating to 550°C. The clayey fraction was also the richest in TOC, and a direct correlation between TOC amount and metal retention was observed.