Yuehua Hu

Phylogenetic analysis of bacterial community composition in sediment contaminated with multiple heavy metals from the Xiangjiang River in China

Understanding the ecology of sediments that are contaminated with heavy metals is critical for bioremediating these sediments, which has become a public concern over the course of the development of modern industry. To investigate the bacterial community composition of sediments that are contaminated with heavy metals in the Xiangjiang River, a total of four sediment samples contaminated with multiple heavy metals were obtained, and a culture-independent molecular analysis, polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), was performed. The results revealed that heavy metal pollution affected the sediment microbial community diversity, and the greatest species diversity appeared in the moderately polluted sediment X sample. The dominant family in these sediments includes α-Proteobacteria, β-Proteobacteria and Firmicutes. Moreover, α-Proteobacteria was significantly increased with increases in heavy metal. A redundancy analysis (RDA) also confirmed this phenomenon.

Adhesion forces between cells of Acidithiobacillus ferrooxidans, Acidithiobacillus thiooxidans or Leptospirillum ferrooxidans and chalcopyrite.

The efficiency of copper leaching is improved by bacteria attached to chalcopyrite. Therefore, the study of the attachment mechanism to control leaching is important. The adhesion of three species of leaching microorganisms including Acidithiobacillus ferrooxidans, Acidithiobacillus thiooxidans and Leptospirillum ferrooxidans to chalcopyrite was investigated by using atomic force microscopy (AFM). The forces were measured with tip-immobilized cells approached to and retracted from the mineral. The results show that both the surface charge and the hydrophobicity of bacteria cells influence the adhesion force. Furthermore, the adhesion force decreased in case the extracellular polymeric substances (EPS) had been removed. In addition, the data indicate that the amount of attached cells increased with increasing adhesion force.

Adsorption of a novel reagent scheme on scheelite and calcite causing an effective flotation separation

The efficient separation of scheelite from calcium-bearing minerals, especially calcite, remains a challenge in practice. In this work, a novel reagent scheme incorporating a depressant of sodium hexametaphosphate (SHMP) and a collector mixture of octyl hydroxamic acid (HXMA-8) and sodium oleate (NaOl) was employed in both single and mixed binary mineral flotation, and it proved to be highly effective for the separation. Furthermore, the role of the pH value in the separation was evaluated. Additionally, the mechanism of the selective separation was investigated systemically via zeta potential measurements, fourier transform infrared (FTIR) spectroscopy analysis, X-ray photoelectron (XPS) spectroscopy analysis and crystal chemistry calculations. It turns out that the selective chemisorption of SHMP on calcite (in the form of complexation between H2PO4-/HPO42- and Ca2+) over scheelite is ascribed to the stronger reactivity and higher density of Ca ions on the commonly exposed surfaces of calcite minerals. The intense adsorption of HXMA-8 on scheelite over calcite due to the match of the OO distances in WO42- of scheelite and CONHOH of HXMA-8 holds the key to the successful separation. We were also interested in warranting the previous claim that NaOl is readily adsorbed on both minerals via chemisorption. Our results provided valuable insights into the application of mixed collectors and an effective depressant for flotation separation.

A review on in situ phytoremediation of mine tailings

Mine tailings are detrimental to natural plant growth due to their physicochemical characteristics, such as high pH, high salinity, low water retention capacity, high heavy metal concentrations, and deficiencies in soil organic matter and fertility. Thus, the remediation of mine tailings has become a key issue in environmental science and engineering. Phytoremediation, an in situ cost-effective technology, is emerging as the most promising remediation method for mine tailings by introducing tolerant plant species. It is particularly effective in dealing with large-area mine tailings with shallow contamination of organic, nutrient and metal pollutants. In this review, the background, concepts and applications of phytoremediation are comprehensively discussed. Furthermore, proper amendments used to improve the physical, chemical and biological properties of mine tailings are systematically reviewed and compared. Emphasis is placed on the types and characteristics of tolerant plants and their role in phytoremediation. Moreover, the role of microorganisms and their mechanism in phytoremediation are also discussed in-depth.

Surface-Charge Anisotropy of Scheelite Crystals

Atomic force microscopy was employed to measure the colloidal interactions between silicon nitride cantilever tips and scheelite crystal surfaces in 1 mM KCl solutions of varying pH. By fitting the Derjguin-Landau-Verwey-Overbeek (DLVO) theoretical model to the recorded force-distance curves, the surface-charge density and surface-potential values were calculated for three crystallographic surfaces including {112}, {101}, and {001}. The calculated surface-potential values were negative in both acidic and basic solutions and varied among crystallographic surfaces. The determined surface-potential values were within zeta-potential values reported in the literature for powdered scheelite minerals. The surface {101} was the most negatively charged surface, followed by {112} and {001}. The surface potential for {001} was only slightly affected by pH, whereas the surface potential for both {112} and {101} increased with increasing pH. Anisotropy in surface-charge density was analyzed in relation to the surface density of active oxygen atoms, that is, the density of oxygen atoms with one or two broken bond(s) within tungstate ions located in the topmost surface layer. On a surface with a higher surface density of active oxygen atoms, a larger number of OH(-) are expected to adsorb through hydrogen bonding, leading to a more negatively charged surface.

The nature of Schwertmannite and Jarosite mediated by two strains of Acidithiobacillus ferrooxidans with different ferrous oxidation ability

Jarosite and Schwertmannite are iron-oxyhydroxysulfate materials. These materials gain increasing interest in geological and metallurgical fields. Especially, for it can effectively scavenge heavy metals, less toxic ions and better biocompatibility, the application potential in environment becomes more and more intriguing. In this study, the nature of Jarosite and Schwertmannite mediates synthesized by two strains of Acidithiobacillus ferrooxidans with different ferrous oxidation ability is investigated. The precipitates are characterized by SEM, XRD, FTIR, and TG/DSC analysis. The materials are varied in color, shape, surface area, elemental composition and crystallinity. The crystallinity of precipitate produced by A. ferrooxidans 23270 with lower oxidation ability in optimized medium is significantly better than the precipitate produced by A. ferrooxidans Gf. A. ferrooxidans Gf will tend to mediate the formation of Schwertmannite with the decreasing of monovalent cation concentration in optimized medium. Cr(VI) adsorption capacity difference exists among the four materials. The adsorption efficiency of Schwertmannite is higher than Jarosite. Adsorption capacity of the materials formed by A. ferrooxidans Gf is higher than that of A. ferrooxidans 23270. Adsorption capacity decreases with the increasing of crystallinity.

Insights into the relation between adhesion force and chalcopyrite-bioleaching by Acidithiobacillus ferrooxidans.

This paper presents a study on the relation between bacterial adhesion force and bioleaching rate of chalcopyrite, which sheds light on the influence of interfacial interaction on bioleaching behavior. In our research, Acidithiobacillus ferrooxidans (A. ferrooxidans) were adapted to grow with FeSO4 · 7H2O, element sulfur or chalcopyrite. Then, surface properties of Acidithiobacillus ferrooxidans and chalcopyrite were analyzed by contact angle, zeta potential and Fourier transform infrared spectroscopy (FTIR). Adhesion force between bacteria and chalcopyrite was measured by atomic force microscopy (AFM). Attachment and bioleaching behaviors were also monitored. The results showed that A. ferrooxidans adapted with chalcopyrite exhibited the strongest adhesion force to chalcopyrite and the highest bioleaching rate. Culture adapted with sulfur bacteria took second place and FeSO4 · 7H2O-adapted bacteria were the lowest. Bioleaching rate and bacterial attachment capacity were positively related to bacterial adhesion force, which is affected by the nature of energy source. According to this work, the attachment of bacteria to chalcopyrite surface is one of the most important aspects that influence the bioleaching process of chalcopyrite.

Effect of chemical composition on electrokinetics of diaspore

The effect of chemical composition of diaspores on their electrokinetics was studied. Increasing SiO(2) content in a diaspore sample was found to decrease its isoelectric point. The X-ray diffraction and SEM microanalysis showed the absence of distinct SiO(2) phases. A linear correlation was found to exist between the measured isoelectric point and alumina to silica mass ratio in diaspore samples. The linear regression analysis of the experimental data suggests a more significant impact of silicon content than aluminum content, indicating a preferential adsorption of dissolved silicon on diaspore samples and/or preferential dissolution of aluminum from diaspore samples.

Selective adsorption of tannic acid on calcite and implications for separation of fluorite minerals

Selective adsorption of tannic acid (TA) on calcite surfaces and the implications of this process for the separation of fluorite ore were studied by microflotation tests, surface adsorption experiments, zeta potential measurements, UV-vis analysis, and X-ray photoelectron spectroscopy (XPS) analysis. The microflotation tests indicated that TA, when added before sodium oleate (NaOl), could selectively depress calcite from fluorite at pH 7. Surface adsorption experiments revealed that TA hinders the interaction of NaOl with calcite. The zeta potential of calcite became more negative with TA than with NaOl. However, the characteristic features of TA adsorption were not observed on fluorite, suggesting that the dominant adsorption sites are dissimilar on the fluorite and calcite surfaces in the pulp. UV-vis spectroscopy, XPS, and solution chemistry analysis were utilized to obtain a better understanding of the mechanism for selective adsorption of TA as well as the key factors determined by the Ca2+ and Ca(OH)+ components on the mineral surfaces. A possible adsorption mechanism along with an adsorption mode is proposed for the surface interaction between TA and calcite.

New insights into the oleate flotation response of feldspar particles of different sizes: Anisotropic adsorption model

The anisotropic adsorption of sodium oleate (NaOL) on feldspar surfaces was investigated to elucidate the different flotation properties of feldspar particles of four different size ranges. Microflotation experiments showed that the feldspar flotation recovery of particles with sizes spanning different ranges decreased in the order 0-19>19-38>45-75>38-45μm. Zeta potential and FTIR measurements showed that NaOL was chemically adsorbed on the Al sites of the feldspar surface. The anisotropic surface energies and broken bond densities estimated by density functional theory calculations showed that, although feldspar mostly exposed (010) and (001) surfaces, only the (001) surfaces contained the Al sites needed for NaOL adsorption. The interaction energies calculated by molecular dynamics simulations confirmed the more favorable NaOL adsorption on (001) than (010) surfaces, which may represent the main cause for the anisotropic NaOL adsorption on feldspar particles of different sizes. SEM measurements showed that the main exposed surfaces on coarse and fine feldspar particles were the side (010) and basal (001) ones, respectively. A higher fraction of Al-rich (001) surfaces is exposed on fine feldspar particles, resulting in better floatability compared with coarse particles. XPS and adsorption measurements confirmed that the Al content on the feldspar surface varied with the particle size, explaining the different NaOL flotation of feldspar particles of different sizes. Therefore, the present results suggest that coarsely ground ore should be used for the separation of feldspar gangue minerals. Further improvements in the flotation separation of feldspar from associated valuable minerals can be achieved through selective comminution or grinding processes favoring the exposure of (010) surfaces.