典型共伴生矿物对黄铜矿生物浸出的影响研究进展

自然界中黄铜矿与金属硫化矿物、金属氧化矿物及一些脉石矿物共伴生。在生物浸出体系中,这些共伴生矿物自身溶解出的离子与黄铜矿之间的原电池效应,以及它们的加入对黄铜矿浸出体系氧化还原电位的影响都会对黄铜矿的浸出效率产生影响。从脉石矿物、金属硫化矿物、金属氧化矿物3个方面综述了共伴生矿物对黄铜矿生物浸出影响的研究现状,旨在为提高黄铜矿浸出效率提供理论支持,并对其他难浸硫化矿的高效选别提供借鉴。

Catalytic removal of volatile organic compounds using ordered porous transition metal oxide and supported noble metal catalysts

Most of volatile organic compounds （VOCs） are harmful to the atmosphere and human health. Cata‐lytic combustion is an effective way to eliminate VOCs. The key issue is the availability of high per‐formance catalysts. Many catalysts including transition metal oxides, mixed metal oxides, and sup‐ported noble metals have been developed. Among these catalysts, the porous ones attract much attention. In this review, we focus on recent advances in the synthesis of ordered mesoporous and macroporous transition metal oxides, perovskites, and supported noble metal catalysts and their catalytic oxidation of VOCs. The porous catalysts outperformed their bulk counterparts. This excel‐lent catalytic performance was due to their high surface areas, high concentration of adsorbed oxy‐gen species, low temperature reducibility, strong interaction between noble metal and support and highly dispersed noble metal nanoparticles and unique porous structures. Catalytic oxidation of carbon monoxide over typical catalysts was also discussed. We made conclusive remarks and pro‐posed future work for the removal of VOCs.

Combined Chemical and Mineralogical Evidence for Heavy Metal Binding in Mining- and Smelting-Affected Alluvial Soils

The binding of metallic contaminants （Pb, Cd, and Zn） and As on soil constituents was studied on four highly contaxninated alluvial soil profiles from the mining/smelting district of Pribram （Czech Republic） using a combination of mineralogical and chemical methods. Sequential extraction analysis （SEA） was supplemented by mineralogical investigation of both bulk samples and heavy mineral fractions using X-ray diffraction analysis （XRD） and scanning electron microscopy with an energy dispersive X-ray spectrometer （SEM/EDS）. The mineralogy of Fe and Mn oxides was studied by voltammetry of microparticles （VMP） and diffuse reflectance spectrometry （DRS）. Zinc and Pb were predominantly bound in the reducible fraction attributed to Fe oxides and Mn oxides （mainly birnessite, Na4Mn14O27.9H2O）, which were detected in soils by XRD and SEM/EDS. In contrast, Cd was the most mobile contaminant and was predominantly present in the exchangeable fraction. Arsenic was bound to the residual and reducible fractions （corresponding to Fe oxides or to unidentified Fe-Pb arsenates）. SEM/EDS observations indicate the predominant affinity of Pb for Mn oxides, and to a lesser extent, for Fe oxides. Thus, a more suitable SEA procedure should be used for these mining-affected soils to distinguish between the contaminant fraction bound to Mn oxides and Fe oxides.

Effect of grinding with sulfur on surface properties and floatability of three nonferrous metal oxides

Co-grinding three nonferrous metal oxides(CuO,PbO and ZnO)with element sulphur under mild conditions and flotation of the ground samples were conducted to investigate the surface properties and floatability of the oxides.Phase transition,morphological features,electrochemical properties and surface chemical compositions of ground samples were studied.The results show that the floatability of CuO is improved after grinding with sulfur,by the formation of surface layer with properties similar to CuS due to the Cu-S bonding.The floatability of PbO is deteriorated after mechanochemical processing due to surface carbonation and the formation of PbS and PbSO4by disproportionation reaction with sulfur.ZnO shows no evident response to mechanochemical sulfidation.

Influence of sulfur addition/solids content ratio on removal of heavy metals from mine tailings by bioleaching

The effect of sulfur addition/solids content(SA/SC)ratio on heavy metals(e.g.copper,zinc and lead)obtained from mine tailings by indigenous sulfur-oxidizing bacteria was studied,and the changes in the chemical forms of heavy metals after bioleaching were explored.The results show that the solubilization of metals is significantly influenced by SA/SC ratio,and SA/SC ratio of 2.50 is found to be the best for bacterial activity and metal solubilization among six SA/SC ratios tested(such as 1.00,1.33,1.50,1.67,2.00 and 2.50)under the chosen experimental conditions.The pH decreases fast and the maximum solubilizations of copper and zinc are respectively 81.76% and 84.35% while that of lead only reaches 40.36%.After bioleaching,the chemical forms of heavy metals have changed.The metals remained in mine tailings are mainly found in residual fractions,which is harmless to the surrounding environment.

Perovskite LaFeO_3 supported bi-metal catalyst for syngas methanation

LaFeO3 perovskite supported Ni and Ni-Fe catalysts were prepared and applied to methanation reaction of syngas. Two preparation methods were employed. One was one-step citrate complexing method, and the other was a two step method using citrate complexing method to produce LaFeO3 and followed by loading nickel oxide on it with impregnation. The structure evolution of the sample as prepared was investigated by XRD, TPR and TEM techniques. For the former, the chemical composites of the calcined sample are NiO-Fe2O3/LaFe1-xNixO3. After reduction and reaction of CO methanation, its composites convert to Fe-Ni@Ni/LaFeO3-La2O2CO3, in which Fe-Ni@Ni is metal particles in nano-size composed of nickel core and Fe-Ni alloy shell. For the latter, the chemical composites of the calcined sample are NiO/LaFeO3; and after reduction and reaction of CO methanation, its chemical composites change to Ni/LaFeO3. Ni/LaFeO3 catalyst is a little more active, while Fe-Ni@Ni/LaFeO3-La2O2CO3 is much more stable and shows very good resistance to carbon deposition. In this work it is aimed to show that the structure and composites of the catalysts can be tailored using perovskite-type oxide as precursor with different preparing method or preparing condition. Therefore, it is a promising route to prepare supported bi-metal catalysts in nano-size for a lot of metals with desired catalytic performances.

Practice and design of the self-purification system for heavy metals-bearing contaminants

Many minerals in nature have self-purification capacity to hold and stabilize deleterious contaminants into their lattice structures,which can be used for treatment of heavy metals-bearing contaminants. Hydrotalcite Layer Double Hydroxide (LDH),tobermorite Calcium Silicate Hydrate (CSH) and apatite are ubiquitous minerals in nature,having higher geochemical stability and potential for binding and stabilizing heavy metals. Based on the elucidation of crystal structure property and self-purification principles of the three minerals above,this article discussed how to design the self-purification system of heavy metal-bearing contaminants.