scholarly journals Separation of Oxidized Pyrrhotite from Fine Fraction Serpentine

Minerals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 472 ◽  
Author(s):  
Jian Zhou ◽  
Yiping Lu ◽  
Guozhi Mao
Keyword(s):  
Zeta Potential ◽  
Photoelectron Spectroscopy ◽  
Nickel Sulfide ◽  
Fine Fraction ◽  
Oxidation Products ◽  
Hydroxyl Groups ◽  
Mineral Surface ◽  
X Ray ◽  
Flotation Recovery ◽  
Sulfide Ore

Abstract: The valuable minerals in copper-nickel sulfide ore can easily be oxidized, leading to the reduction of their flotation recovery and a difficulty in separating them from gangue. In order to solve the problem, the reaction mechanism of the octanohydroxamic acid (OHA) on oxidized pyrrhotite was revealed through micro-flotation, adsorption tests, zeta potential measurements, and X-ray photoelectron spectroscopy (XPS) analysis. The results show that this is a feasible way to find a suitable collector that can directly react to oxidation products on the surface of pyrrhotite. OHA can efficiently reclaim oxidized pyrrhotite and achieve the selective separation of a pyrrhotite-serpentine mixture in a weak alkaline environment. The adsorption tests, zeta potential measurements, and XPS analyses show that OHA can interact with an oxidized pyrrhotite surface, and the interaction between OHA and serpentine is very weak. The XPS analyses indicate that the OHA collector can chelate with Fe(OH)3 on the surface of oxidized pyrrhotite and form an “O, O” five-ring chelate. At the same time, the OHA collector may compete with the hydroxyl groups of hydrophilic substances on the mineral surface to produce hydrophobic products and reduce the hydrophilic substances on the mineral surface.

scholarly journals Polyarylene Ether Nitrile and Barium Titanate Nanocomposite Plasticized by Carboxylated Zinc Phthalocyanine Buffer

Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 418 ◽  
Author(s):  
Shuning Liu ◽  
Chenchen Liu ◽  
Changyu Liu ◽  
Ling Tu ◽  
Yong You ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Barium Titanate ◽  
Photoelectron Spectroscopy ◽  
Energy Dispersive Spectrometer ◽  
Composite Films ◽  
Zinc Phthalocyanine ◽  
Hydroxyl Groups ◽  
X Ray ◽  
Polyarylene Ether Nitrile ◽  
High Dielectric

Barium titanate (BT) and polyarylene ether nitrile (PEN) nanocomposites with enhanced dielectric properties were obtained by using carboxylatedzinc phthalocyanine (ZnPc-COOH) buffer as the plasticizer. Carboxylated zinc phthalocyanine, prepared through hydrolyzing ZnPc in NaOH solution, reacted with the hydroxyl groups on the peripheral of hydrogen peroxide treated BT (BT-OH) yielding core-shell structured BT@ZnPc. Thermogravimetric analysis (TGA), transmission electron microscopy (TEM), TEM energy dispersive spectrometer mapping, scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared (FTIR) demonstrated successful preparation of BT@ZnPc. The fabricated BT@ZnPc was incorporated into the PEN matrix through the solution casting method. Rheological measurements demonstrated that the ZnPc-COOH buffer can improve the compatibility between BT and PEN effectively. With the existence of the ZnPc-COOH buffer, the prepared BT@ZnPc/PEN nanocomposites exhibit a high dielectric constant of 5.94 and low dielectric loss (0.016 at 1000 Hz). BT@ZnPc/PEN dielectric composite films can be easily prepared, presenting great application prospects in the field of organic film capacitors.

scholarly journals Activation Mechanism of Lead Ions in Perovskite Flotation with Octyl Hydroxamic Acid Collector

Minerals ◽  
2018 ◽  
Vol 8 (8) ◽  
pp. 341 ◽  
Author(s):  
Yu Zheng ◽  
Yating Cui ◽  
Weiqing Wang
Keyword(s):  
Zeta Potential ◽  
Photoelectron Spectroscopy ◽  
Hydroxamic Acid ◽  
Relative Content ◽  
Lead Ions ◽  
Activation Mechanism ◽  
X Ray ◽  
Ft Ir ◽  
Acidic Conditions ◽  
Ir Analysis

The activation mechanism of lead ions (Pb2+) in perovskite flotation with an octyl hydroxamic acid collector was systematically investigated using microflotation experiments, zeta-potential measurements, adsorption tests, Fourier transform infrared (FT-IR) analysis, and X-ray photoelectron spectroscopy (XPS) analysis. The results of microflotation experiments and adsorption tests indicate that the presence of Pb2+ can promote the adsorption of octyl hydroxamic acid (OHA) on the perovskite surface and enhance the flotability of perovskite under weakly acidic conditions. The maximum recovery of 79.62% was obtained at pH 6.5 in the presence of Pb2+, and the maximum recovery of 57.93% was obtained at pH 5.7 without Pb2+. At pHs below 7, lead species are mainly present as Pb2+ and PbOH+ in the solution; besides this, the relative content of titanium increases on the perovskite surface. The adsorption of Pb2+ and PbOH+ on the perovskite surface makes the zeta-potential of perovskite shift positively, and increases the number of activated sites on the perovskite surface. FT-IR and XPS analyses confirm that OHA chemisorbs on the surface of Pb2+-activated perovskite and forms hydrophobic Pb-OHA complexes, which improve the flotability of perovskite.

scholarly journals Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO2 Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel

Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2209 ◽  
Author(s):  
Jing Liu ◽  
Xiao-Min Li ◽  
Jing He ◽  
Lu-Ying Wang ◽  
Jian-Du Lei
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Photocatalytic Oxidation ◽  
Uv Light ◽  
Sulfur Removal ◽  
Oxidation Products ◽  
Core Shell ◽  
Adsorptive Desulfurization ◽  
X Ray ◽  
Tio2 Microspheres

A core-shell Cu-benzene-1,3,5-tricarboxylic acid (Cu-BTC)@TiO2 was successfully synthesized for photocatalysis-assisted adsorptive desulfurization to improve adsorptive desulfurization (ADS) performance. Under ultraviolet (UV) light irradiation, the TiO2 shell on the surface of Cu-BTC achieved photocatalytic oxidation of thiophenic S-compounds, and the Cu-BTC core adsorbed the oxidation products (sulfoxides and sulfones). The photocatalyst and adsorbent were combined using a distinct core-shell structure. The morphology and structure of the fabricated Cu-BTC@TiO2 microspheres were verified by scanning electron microscopy, high-resolution transmission electron microscopy, energy-dispersive x-ray spectroscopy, X-ray powder diffraction, nitrogen adsorption-desorption and X-ray photoelectron spectroscopy analyses. A potential formation mechanism of Cu-BTC@TiO2 is proposed based on complementary experiments. The sulfur removal efficiency of the microspheres was evaluated by selective adsorption of benzothiophene (BT) and dibenzothiophene (DBT) from a model fuel with a sulfur concentration of 1000 ppmw. Within a reaction time of 20 min, the BT and DBT conversion reached 86% and 95%, respectively, and achieved ADS capacities of 63.76 and 59.39 mg/g, respectively. The BT conversion and DBT conversion obtained using Cu-BTC@TiO2 was 6.5 and 4.6 times higher, respectively, than that obtained using Cu-BTC. A desulfurization mechanism was proposed, the interaction between thiophenic sulfur compounds and Cu-BTC@TiO2 microspheres was discussed, and the kinetic behavior was analyzed.

scholarly journals X-Ray Photoelectron Spectroscopy Study of Silane Coupling Agents/Basalt Fiber Interface

2011 ◽  
Vol 236-238 ◽  
pp. 1467-1471 ◽  
Author(s):  
Ya Lan Liu ◽  
Shi Jie Shen ◽  
Li Zhang ◽  
Ling Min Shao
Keyword(s):  
Coupling Agent ◽  
Photoelectron Spectroscopy ◽  
Silane Coupling Agent ◽  
Basalt Fiber ◽  
Fiber Surface ◽  
Chemical Compositions ◽  
Hydroxyl Groups ◽  
Silane Coupling Agents ◽  
X Ray ◽  
Silane Coupling

In this paper, two types of fiber surface treatment methods, namely heat treatment and chemical coupling, were used to improve the basalt fiber surface properties. The basalt fiber surface was heated under 250Celsius degree for 30minites, and then was treated by silane coupling agent ethanol solution with different concentrations. X-ray photoelectron spectroscopy (XPS) was utilized to study the surface chemical compositions of basalt fiber after treatments. The XPS analysis indicated that chemical bonds between basalt fiber and KH-550 have occurred, and silanols were adsorbed to the surface of basalt fibers by an ether linkage between the silanols and the hydroxyl groups of the fibers. When the concentration of KH-550 is 0.8wt%, the optimal bonding condition is formed between basalt fiber and silane coupling agent.

scholarly journals Preparation of Ni Doped ZnO-TiO2Composites and Their Enhanced Photocatalytic Activity

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Xiaowen Zou ◽  
Xiaoli Dong ◽  
Limei Wang ◽  
Hongchao Ma ◽  
Xinxin Zhang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Sol Gel ◽  
Visible Region ◽  
Hydroxyl Groups ◽  
X Ray ◽  
Surface Hydroxyl ◽  
Simulated Solar Light ◽  
Transmission Electron ◽  
Doped Zno

Herein, Ni doped ZnO-TiO2composites were prepared by facile sol-gel approach and were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-visible diffuse reflectance spectroscopy (UV-Vis DRS), X-ray photoelectron spectroscopy (XPS), and photoluminescence spectroscopy (PL). The results indicated that the Ni ions can be incorporated into the lattice of TiO2structure and replace Ti. The introduction of Ni expanded light absorption of TiO2to visible region, increased amount of surface hydroxyl groups and physically adsorbed oxygen (as the electronic scavenges), and then enhanced separation rate of photogenerated carriers. The photodegradation test of reactive brilliant blue (KN-R) under simulated solar light indicated that Ni doped ZnO-TiO2composites have better photocatalytic activities, as compared to those of TiO2and ZnO-TiO2.

scholarly journals Effects of Galvanic Interaction between Chalcopyrite and Monoclinic Pyrrhotite on Their Flotation Separation

Minerals ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 39
Author(s):  
Liu Yang ◽  
Xiaowen Zhou ◽  
Huashan Yan ◽  
Hongliang Zhang ◽  
Xiaohe Liu ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
The Other ◽  
X Ray ◽  
Flotation Recovery ◽  
Xps Characterization ◽  
Monoclinic Pyrrhotite ◽  
Galvanic Interaction ◽  
Monomineral Flotation ◽  
Sem Test ◽  
Scanning Electron

The galvanic interaction between chalcopyrite and monoclinic pyrrhotite and its effect on flotation separation were studied using monomineral flotation tests, adsorption capacity tests, X-ray photoelectron spectroscopy (XPS) characterization, and scanning electron microscopy (SEM) test. These results showed that the interaction promoted the reduction of O2 on the cathodic chalcopyrite surface and accelerated the generation of Fe(OH)3, which was not conducive to collector adsorption; hence, the flotation recovery decreased by 10–16%. On the other hand, galvanic interaction accelerated the oxidation of S on the anodic monoclinic pyrrhotite surface to S0 or SO42− and produced a large amount of H+, thus preventing the formation of Fe(OH)3. Meanwhile, the Cu2+ eluted from chalcopyrite surface activated monoclinic pyrrhotite; hence, the flotation recovery increased by 3–10%. Galvanic interaction reduced the floatability difference between the two minerals, and the separation difficulty was significantly increased. Even with an increase in the amount of lime, the separation could not be improved.

scholarly journals The Auxiliary Effect of Copper Ions on the Depressant Effect of Sodium Thioglycolate in Chalcopyrite Flotation

Minerals ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 157
Author(s):  
Chonghui Zhang ◽  
Tingshu He ◽  
Wei Chen ◽  
Xianzhong Bu ◽  
Sen Wang ◽  
...  
Keyword(s):  
Zeta Potential ◽  
Photoelectron Spectroscopy ◽  
Active Sites ◽  
Copper Ions ◽  
Depressant Effect ◽  
X Ray ◽  
Adsorption Sites ◽  
Effect Of Copper ◽  
Adsorption Layers ◽  
Hydrophobic Substance

Sodium thioglycolate is a chalcopyrite depressant, but its depressant effect is weak. The paper investigated the effect of CuSO4 on the depressant performance of sodium thioglycolate towards chalcopyrite through flotation tests, Zeta potential measurements, X-ray photoelectron spectroscopy (XPS) analyses and Fourier-transform infrared (FTIR) spectra measurements. It was found that copper ions could improve the depressant effect of sodium thioglycolate on chalcopyrite. The results showed that copper ions could adsorb on the surface of chalcopyrite and form mixed copper sulfide and cupric oxides/hydroxides adsorption layers. As a result, the mineral composition on the chalcopyrite surface was changed. With sodium thioglycolate treatment, the Zeta potential and the adsorption sites of chalcopyrite surface were both increased, and the hydrophobic substance Sn2−/S0 concentration was decreased. The electrostatic repulsion of chalcopyrite surface with sodium thioglycolate was also decreased, which made the sodium thioglycolate interact with chalcopyrite more easily. The more active sites could adsorb more sodium thioglycolate, which improved the hydrophilia of chalcopyrite. At the same time, the decrease of Sn2−/S0 concentration could further improve the hydrophilia of chalcopyrite. The results show that the copper ions could exhibit auxiliary effect with sodium thioglycolate and could further enhance the depressant effect of sodium thioglycolate on the chalcopyrite flotation. This paper provides new insights into the depression of chalcopyrite flotation by sodium thioglycolate.

scholarly journals X-ray Photoelectron Spectroscopy in Mineral Processing Studies

2020 ◽  
Vol 10 (15) ◽  
pp. 5138
Author(s):  
Yuri Mikhlin
Keyword(s):  
Spatial Resolution ◽  
Photoelectron Spectroscopy ◽  
Surface Characterization ◽  
Ambient Pressure ◽  
Surface Characteristics ◽  
Mineral Processing ◽  
Oxidation Products ◽  
X Ray ◽  
Flotation Collectors ◽  
Solid Liquid

Surface phenomena play the crucial role in the behavior of sulfide minerals in mineral processing of base and precious metal ores, including flotation, leaching, and environmental concerns. X-ray photoelectron spectroscopy (XPS) is the main experimental technique for surface characterization at present. However, there exist a number of problems related with complex composition of natural mineral systems, and instability of surface species and mineral/aqueous phase interfaces in the spectrometer vacuum. This overview describes contemporary XPS methods in terms of categorization and quantitative analysis of oxidation products, adsorbates and non-stoichiometric layers of sulfide phases, depth and lateral spatial resolution for minerals and ores under conditions related to mineral processing and hydrometallurgy. Specific practices allowing to preserve volatile species, e.g., elemental sulfur, polysulfide anions and flotation collectors, as well as solid/liquid interfaces are surveyed; in particular, the prospects of ambient pressure XPS and cryo-XPS of fast-frozen wet mineral pastes are discussed. It is also emphasized that further insights into the surface characteristics of individual minerals in technological slurries need new protocols of sample preparation in conjunction with high spatial resolution photoelectron spectroscopy that is still unavailable or unutilized in practice.

scholarly journals Mg-Al Mixed Oxide Adsorbent Synthesized Using FCT Template for Fluoride Removal from Drinking Water

2019 ◽  
Vol 2019 ◽  
pp. 1-11 ◽  
Author(s):  
Jifa Liu ◽  
Ping Zhao ◽  
Yue Xu ◽  
Xibin Jia
Keyword(s):  
Drinking Water ◽  
Adsorption Capacity ◽  
Mixed Oxide ◽  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Molar Ratio ◽  
Fluoride Removal ◽  
Hydroxyl Groups ◽  
X Ray ◽  
Fluoride Adsorption

To make full use of natural waste, a novel Mg-Al mixed oxide adsorbent was synthesized by the dip-calcination method using the fluff of the chinar tree (FCT) and an Mg(II) and Al(III) chloride solution as raw materials. The adsorbents were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectroscopy, and X-ray photoelectron spectroscopy (XPS). The effects of the Mg/Al molar ratio and calcination temperature on the performance of the novel Mg-Al mixed oxide adsorbent were investigated. The optimized Mg-Al mixed oxide adsorbent had a Langmuir adsorption capacity of 53 mg/g. This adsorption capacity was higher than that of the separate Mg oxide and Al oxide. The synergy between Mg and Al is beneficial to the adsorption performance of the material. The fluoride adsorption capacity of the optimized Mg-Al mixed oxide adsorbent is only slightly affected by ions such as Cl−, NO3−, SO42−, Na+, and K+and is excellent for use in recycling and real water. The hydroxyl groups on the surface of the Mg-Al mixed oxide adsorbent play a key role in the adsorption of fluorine. The as-obtained novel Mg-Al mixed oxide adsorbent is an efficient and environmentally friendly agent for fluoride removal from drinking water.

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