Current situation and prospects for the clean utilization of gold tailings.

Gold tailings are characterized by low-grade, complex composition, fine embedded particle size, environmental pollution, and large land occupation. This paper describes the mineralogical properties of gold tailings, including chemical composition, phase composition, particle size distribution, and microstructure; summarizes the recycling and utilization of components such as mica, feldspar, and valuable metals in gold tailings; reviews harmless treatment measures for harmful elements in gold tailings; and adumbrated the research progress of gold tailings in the application fields of building materials, ceramics, and glass materials. Based on these discussions, a new technology roadmap that combines multistage magnetic separation and cemented filling is proposed for the clean utilization of all components of gold tailings.

Eco-friendly approach for enhancing the floatability of non-metallic components in waste printed circuit boards: Adding gutter oil during dry grinding.

Waste printed circuit boards (WPCBs) are an attractive secondary resource that is challenging to dispose of due to its complexity. Reverse flotation is an effective method to remove non-metallic particles (NMPs) to obtain metals from WPCBs. Nevertheless, the removal of NMPs is usually inadequate in the present flotation practice. Thus, to provide a clean approach to improve the removal efficiency of NMPs, the method of adding gutter oil during dry grinding process was adopted to enhance the hydrophobic sites on the surface of NMPs to improve the floatability. The surface morphology of NMPs was analyzed by SEM, the results show that the rough morphology inhibited the adhesion of bubbles, while water occupied the cracks and pores, making it challenging for collector adsorption, which result in unstable particle-bubble adhesion. The results of FTIR indicate that both NMPs and gutter oil have -CH3, -CH2, -C = O, -C-O functional groups, which promotes the adsorption of gutter oil on the surface of NMPs. The contact angle (CA) results show that the adsorption of gutter oil on the particle surface is conducive to the formation of enhanced CA. Furthermore, the flotation enhancement effect was verified by flotation kinetic experiments. The accumulated floats yield of NMPs conditioned by gutter oil during grinding is increased from 67.05% (NMPs without conditioning) to 95.02%, and the resin recovery is increased by 31.10%. It is demonstrated that dry grinding with gutter oil can strengthen the floatability of NMPs, which provides a potential approach to increase the flotation efficiency of WPCBs.

Synthesized Zeolite Based on Egyptian Boiler Ash Residue and Kaolin for the Effective Removal of Heavy Metal Ions from Industrial Wastewater.

The increase of global environmental restrictions concerning solid and liquid industrial waste, in addition to the problem of climate change, which leads to a shortage of clean water resources, has raised interest in developing alternative and eco-friendly technologies for recycling and reducing the amount of these wastes. This study aims to utilize Sulfuric acid solid residue (SASR), which is produced as a useless waste in the multi-processing of Egyptian boiler ash. A modified mixture of SASR and kaolin was used as the basic component for synthesizing cost-effective zeolite using the alkaline fusion-hydrothermal method for the removal of heavy metal ions from industrial wastewater. The factors affecting the synthesis of zeolite, including the fusion temperature and SASR: kaolin mixing ratios, were investigated. The synthesized zeolite was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), particle size analysis (PSD) and N2 adsorption-desorption. The SASR: kaolin weight ratio of 1:1.5 yields faujasite and sodalite zeolite with 85.21% crystallinity, which then shows the best composition and characteristics of the synthesized zeolite. The factors affecting the adsorption of Zn2+, Pb2+, Cu2+, and Cd2+ ions from wastewater on synthesized zeolite surfaces, including the effect of pH, adsorbent dosage, contact time, initial concentration, and temperature, have been investigated. The obtained results indicate that a pseudo-second-order kinetic model and Langmuir isotherm model describe the adsorption process. The maximum adsorption capacities of Zn2+, Pb2+, Cu2+, and Cd2+ ions onto zeolite at 20 °C were 12.025, 15.96, 12.247, and 16.17 mg·g-1, respectively. The main mechanisms controlling the removal of these metal ions from aqueous solution by synthesized zeolite were proposed to be either surface adsorption, precipitation, or ion exchange. The quality of the wastewater sample obtained from the Egyptian General Petroleum Corporation (Eastern Desert, Egypt) was highly improved using the synthesized zeolite and the content of heavy metal ions was significantly reduced, which enhances the utilization of the treated water in agriculture.

WSe2-loaded co-catalysts Cu3P and CNTs: Improving photocatalytic hydrogen precipitation and photocatalytic memory performance.

Photocatalytic decomposition of water for hydrogen production using semiconductor photocatalysts in visible light is considered one of the most promising environmentally friendly ways to produce hydrogen. In this work, the calcination method was adopted to prepare an efficient Cu3P/WSe2/CNTs composite photocatalysts. Cu3P and carbon nanotubes (CNTs) were used as co-catalysts to reduce the composite rate of the photogenerated supports of the photocatalyst. The unique metallic properties of Cu3P as a transition metal phosphide makes it a cost-effective alternative to noble metal co-catalysts. CNTs can serve both as co-catalysts and as a suitable carrier to accelerate the transfer rate of photogenerated electrons. The experimental results showed that the Cu3P/WSe2/CNTs composite photocatalyst exhibited stronger activities in photocatalytic hydrogen production than pure WSe2. In particular, a higher quantum yield of 30.27% at the range 400-700 nm was achieved with a loading of 4% CNTs, a calcination temperature of 300 °C and a calcination time of 2.0 h. In contrast, the quantum yield of pure WSe2 was only 14.01%. The highest hydrogen production rate was 6.987 mL in 4.0 h, and the average hydrogen production rate was 712.985 µmol·h-1g-1, which was 2.39 times higher than that of pure WSe2.The catalytic memory performance of the composite samples was also examined. The results indicated that the best catalytic memory performance was achieved under the pre-illumination condition of 5.0 h. The amount of hydrogen produced under darkness for 4.0 h was up to 4.934 mL and the average hydrogen production rate was 503.454 µmol·h-1g-1. The average hydrogen production rate was 1.69 times higher than the average hydrogen production rate of pure WSe2 under light conditions.

Enhanced cleaner flotation behavior of non-metallic particles in waste printed circuit boards: From the perspective of particle size.

Flotation is an attractive method for separating the different components of waste printed circuit boards (WPCBs) due to its cleanliness and efficiency. Non-metallic particles (NMPs) with good floatability usually need to be floated, however, it is difficult to achieve complete removal. The effect of particle size on the flotation behavior of NMPs, which is usually ignored in previous studies, is concerned in this paper. Flotation tests and kinetic analysis were carried out to reveal the effect of reagent dosage on flotation characteristics of particles in narrow size fractions. As the fineness decreases, the particles are more likely to be floated. Equally, the finer the particle size, the lower the reagent dosage required to achieve the maximum recovery. For 1-0.5 mm and -0.045 mm, the maximum recovery increased from 42.16% (1500 g/t MIBC) to 97.31% (100 g/t MIBC). Therefore, the feasibility of reducing particle size by grinding to improve floatability was verified. The results show that the reduction of particle size can significantly promote its efficiency of being floated. After grinding treatment, -0.045 mm yields in each size fraction (1-0.5, 0.5-0.25, 0.25-0.125, 0.125-0.074, 0.074-0.045 mm) increased by 22.10%, 28.42%, 30.90%, 64.56%, 89.32%, resulting in an increase of 37.71%, 13.12%, 2.82%, 7.82% and 2.00% in maximum recovery, respectively. It is also proved that the particle size, rather than the resin content, has a more significant effect on the floatability of NMPs.

Does microplastic really represent a threat? A review of the atmospheric contamination sources and potential impacts.

Microplastics (MPs) are regarded as one of the major atmospheric contaminants that have gained wide attention across the globe in the current dispensation. Airborne MPs have been collected in atmospheric fallouts, in indoor and outdoor air as well as along roadways and indoor dust. The most dominating constituent shapes and forms of identified airborne MPs are fibers and synthetic textiles, respectively. With the breathing mechanism as a spontaneous practice for survival, the inhalation of airborne MPs is an inevitable deal. The level of toxicity of MPs to organisms stems from its physiochemical speciation. The smaller size and almost weightless nature make it possible to suspend in the atmosphere and be inhaled and create potential health problems. Nonetheless, the data available concerning the presence of airborne MPs and its environmental and human health impacts is limited. In this review, we extensively discuss the rigorous and suitable methodologies adopted for the analysis of airborne MPs in previous studies. The characteristics and sources of airborne MPs, the potential health impacts on humans, and some mitigating measures have also been discussed thoroughly.

Kelp-derived N-doped biochar activated peroxymonosulfate for ofloxacin degradation.

N-doped carbon materials have been proven to be effective catalysts for activating peroxymonosulfate (PMS). Marine algae biomass is rich in nitrogenous substances , which can reduce the cost of N-doping process and can obtain excellent N-doped catalysts cheaply and easily. In this study, kelp biomass was selected to prepare N-doped kelp biochar (KB) materials. The high defect degree, high specific surface area, and participation of graphite N make KB have excellent catalytic degradation ability. The KB degraded 40 mg/L ofloxacin (OFL) close to 100% within 60 min, applied with PMS. Through quenching experiments and electron paramagnetic resonance spectroscopy, the degradation process dominated by non-radical pathways was determined. At the same time, O2·- and 1O2 were closely related, and a significant impact of quenching O2·- on the reaction was observed. The non-radical approach made the system excellent performance over a wide pH range and in the presence of multiple anions. The experiments of reusability confirmed the stability of the material. Its catalytic performance was restored after low-temperature pyrolysis. This research supports the use of endogenous nitrogen in biomass. It provides more options for advanced oxidation process application and marine resource development.

Advanced utilization of copper in waste printed circuit boards: Synthesis of nano-copper assisted by physical enrichment.

The copper in the waste printed circuit boards (WPCBs) is cleanly recycled by physical methods and presented in the form of nano copper particles by hydrometallurgical, which provides environmental approach to the advanced utilization of metal copper. Copper in WPCBs was first pre-concentrated by gradient enrichment process including gravity separation, mechanical grinding and flotation. The leaching method was then used to dissolve copper from the flotation concentrate in ammoniacal/ammonium salt solutions. Subsequently, reduction treatment was conducted to synthesize nano-copper from leaching solution. The enrichment results of the clean physical separation process show that the grade of copper increased from 16.22% to -38.05% by gravity separation, and the grade of copper further increased to 72.62 % by flotation after dissociation, which avoids overgrinding of low value components. Copper nanoparticles can be prepared effectively, and the recovery of copper in the leaching process reaches 99 %. The particle size of copper nanoparticles obtained by ascorbic acid reduction is tens of nanometers, and the surface of copper nanoparticles is smooth and nearly spherical. The present study proposes an environmentally friendly process of preparing nano-copper from the copper in WPCBs.

Mechanical activation to enhance the natural floatability of waste printed circuit boards.

The metal in the waste printed circuit boards (WPCBs) is an excellent secondary metal resource. WPCBs were ground to dissociate, and impurities in the dissociated product were removed by gradient flotation to recover valuable metals in this study. The effects of crushing methods on size composition and dissociation state of the crushed products were studied. Then the gradient flotation experiment was designed to verify the natural floatability of ground materials. Grinding test shows that impact crushing has greater grinding fineness (-0.074 mm) than shear crushing, which is 42.14% and 26.18% respectively with 5 min grinding. The flotation test results illustrate that the natural floatability of impurities increases with the grinding fineness, that is, the yield of floats increases without flotation reagents. For impact crushing and shear crushing, the floats yields are 38.48% and 31.75% respectively, accompanied by 70.53% and 65.46% impurity removal for ground materials with 5 min grinding. Subsequently, 21.61% and 26.35% of impurities can be further removed with the aid of collector. Finally, the recovery of Cu in concentrate reaches 67.84% and 65.75%, respectively. FT-IR proves that the excellent floatability of particles is caused by the significant hydrophobic group. Mechanical grinding has been proved to have double effects of improving dissociation and natural floatability.

Flotation dynamics of metal and non-metal components in waste printed circuit boards.

Flotation is an effective and clean separation technology to realize the recovery of metal in waste printed circuit boards (WPCBs). The flotation kinetic of metal and non-metal components was concerned in this study. In addition, the loading of bubbles, the collision and shedding of particles and bubbles were used to assist in proving the particle dynamics results. By analyzing the force on the particles, the load of bubbles on particles was analyzed, and the appropriate volume ratio of bubbles to particles was 1.5-8.0, depending on the particle density. Moreover, Clift model and Schiller-Naumann model has high fitting accuracy for the final bubble velocity. In addition, metal particles have greater settling velocity, which results in shorter collision time with bubbles. In the process of bubble-particle rising, the shedding probability gradually decreases, and the shedding probability of metal particles is much higher than that of non-metal particles. The results of flotation kinetics show that the removal of impurity particles represented by silicon mainly occurs in the initial stage of flotation process. The loss of copper increases with flotation time and collector dosage. This study reveals the flotation kinetics of particles from the perspectives of bubble loading, bubble-particle collision and shedding.

Enhanced Photocatalytic Activity of SiC-Based Ternary Graphene Materials: A DFT Study and the Photocatalytic Mechanism.

A graphene-like semiconductor composite is one of the most promising photocatalyst that does not use noble metals. These composites have excellent photocatalytic properties and have attracted great attention for water splitting. Here, a facile method called the hydrothermal method was used to prepare graphene oxide (GO)/SiC/MoS2 composites. Under visible-light irradiation, the GO/SiC/MoS2 composite had excellent photocatalytic production of hydrogen from water splitting. In particular, the catalyst added 8 wt % of Mo weight yielded the highest quantum of 20.45% at 400-700 nm of wavelength. A positive synergistic effect between the layered GO and MoS2 components contributed to the enhanced photoactivity of the SiC particles. The synergistic effect reduced the recombination of photogenerated holes and electrons, enhanced the rate of electron transfer, and provided more reaction active sites for water splitting. The interactions among SiC, GO, and MoS2 were investigated using a density functional theory. The calculations showed that the relative positions between graphene only slightly affect the stability of the interface, and the MoS2 layers have a great influence. The photocatalytic mechanism was also discussed, and electron transfer was predicted.

Determination and detoxification of cyanide in gold mine tailings: A review.

Cyanide is among the most toxic chemicals widely employed in the cyanidation process to leach precious minerals, such as gold and silver, by the minerals processing companies worldwide. This present article reviews the determination and detoxification of cyanide found in gold mine tailings. Most of the cyanide remains in the solution or the slurries after the cyanidation process. The cyanide species in the gold tailings are classified as free cyanide, weak acid dissociation, and metallocyanide complexes. Several methods, such as colorimetric, titrimetric, and electrochemical, have been developed to determine cyanide concentrations in gold mine effluents. Application of physical, natural, biological, and chemical methods to detoxify cyanide to a permissible limit (50 mg L-1) can be achieved when the chemical compositions of cyanide (type of species) present in the tailings are known. The levels of cyanide concentration determine the impact it will have on the environment.

Effect of Layer Charge Density on Hydration Properties of Montmorillonite: Molecular Dynamics Simulation and Experimental Study.

Four kinds of Ca-montmorillonite with different layer charge density were used to study the effect of charge density on their hydration properties by molecular dynamics simulation and experiments. The research results of Z-density distribution of water molecules, Hw (hydrogen in water molecules), and Ca in the interlayer of montmorillonite show that the hydration properties of montmorillonite are closely related to its layer charge density. If the charge density is low, the water molecules in the interlayers are mainly concentrated on the sides of the central axis about -1.3 Å and 1.5 Å. As the charge density increases from 0.38semi-cell to 0.69semi-cell, the water molecules are distributed -2.5 Å and 2.4 Å away from the siloxane surface (Si-O), the concentration of water molecules near the central axis decreases, and at the same time, Ca2+ appears to gradually shift from the vicinity of the central axis to the Si-O surface on both sides in the montmorillonite layer. The simulation results of the radial distribution function (RDF) of the Ca-Hw, Ca-Ow (oxygen in water molecules), and Ca-Ot (the oxygen in the tetrahedron) show that the Ca2+ and Ow are more tightly packed together than that of Hw; with the increase of the charge density, due to the fact that the negative charge sites on the Si-O surface increase, under the action of electrostatic attraction, some of the Ca2+ are pulled towards the Si-O surface, which is more obvious when the layer charge density of the montmorillonite is higher. The results of the RDF of the Ot-Hw show that with the increase of charge density, the number of hydrogen bonds formed by Ot and Hw in the interlayers increase, and under the action of hydrogen bonding force, the water molecules near the central axis are pulled towards the two sides of Si-O surface. As a result, the arrangement of water molecules is more compact, and the structure is obvious. Correspondingly, the self-diffusion coefficient shows that the higher the layer charge density, the lower the self-diffusion coefficient of water molecules in interlayers is and the worse the hydration performance of montmorillonite. The experimental results of the experiments fit well with the above simulation results.

Effect of Layer Charge Characteristics on the Distribution Characteristics of H2O and Ca2+ in Ca-Montmorillonites Interlayer Space: Molecular Dynamics Simulation.

The charge characteristics of montmorillonite have significant effects on its hydration and application performances. In this study, a molecular dynamics simulation method was used to study the influence of the charge position and charge density of montmorillonite on the distribution of H2O and Ca2+ in layers. The results showed that when the layer charge is mainly derived from the substitution among ions in the tetrahedron, a large number of Hw and Ot are combined into a hydrogen bond in the interlayer, thus the water molecules are more compactly arranged and the diffusion of water molecules among the layers is reduced. In addition, the Ca2+ are diffused to the sides by a concentrated distribution in the central axis of the layer. As the charge density of the montmorillonite increases, the polarity of the Si-O surface increases, which lesds to the deterioration of the diffusibility of the water molecules and the structure of the water molecules in the interlayers is more stable. The increase in the layer charge density lesds to the expansion of the isomorphic substitution range of the crystal structure, which results in a more dispersed distribution of Ca2+ among the layers under the action of electrostatic attraction between the substituted negative sites and the Ca2+.

Cr-Dopant Induced Breaking of Scaling Relations in CoFe Layered Double Hydroxides for Improvement of Oxygen Evolution Reaction.

Monodentate adsorption of oxygen intermediates results in a theoretical overpotential limit of ≈0.35 V for oxygen evolution reaction (OER), which causes the sluggish kinetics of the OER process. In this work, nonprecious chromium dopant is introduced into the self-supported CoFe layered double hydroxides (LDHs) on nickel foam (Cr-CoFe LDHs/NF) via a facile one-step hydrothermal method, which exhibits a preeminent electrocatalytic activity toward the OER with an ultralow overpotential of 238 mV to obtain 10 mA cm-2 and a high stability after cyclic voltammetry for 5000 cycles in alkaline solution (1 m KOH). Density functional theory (DFT) calculations unveil that Cr dopants as new active sites could improve the electron-donation ability of the resultant Cr-CoFe LDHs due to the smaller electronegativity of Cr in comparison with Fe and Co. Therefore, the scaling relation of adsorption energy among four oxygen intermediates is broken and consequently the OER performance is further promoted. This work provides a strategy to develop efficient metal layered double hydroxide OER catalysts.

Recovery of metals in waste printed circuit boards by flotation technology with soap collector prepared by waste oil through saponification.

Recycling metal from waste printed circuit boards (WPCBs) through green flotation technology has been concerned in this paper. For the sake of environmentally friendly of flotation process, a renewable collector was prepared from waste oil by saponification reaction. The collector composition was analyzed by GC-MS, and results show that the main compositions are n-Hexadecanoic acid, oleic acid and octadecanoic acid. XRD and XRF results show that copper is the main valuable element for recovery. Effects of collector dosage and pH on flotation behavior were analyzed. In addition, the feasibility of improving copper recovery by multiple sorting test processes was also verified. Flotation results show that the concentrate yield and metal recovery decreases with the increase of collector dosage, accompanied by the increase of copper grade. When the dosage of collector is 3 kg/t, concentrate with 22% yield, 66% copper grade, and 47% copper recovery is obtained. Furthermore, concentrate yield and metal recovery rate first decrease and then increase with the increase of pH, while copper content first increase and then decrease. The suitable pH of the separation process is neutral environment (pH = 6-8). The study provides an alternative process for the recovery of metals in WPCBs.

Flexible vanadium-doped Ni2P nanosheet arrays grown on carbon cloth for an efficient hydrogen evolution reaction.

Tuning the electronic structure, morphology, and structure of electrocatalysts is of great significance to achieve a highly active and stable hydrogen evolution reaction (HER). Herein, combining hydrothermal and low temperature phosphidation methods, V-doped Ni2P nanosheet arrays grown on carbon cloth (V-Ni2P NSAs/CC) were successfully prepared for the HER. It is found that the prepared V-Ni2P NSAs/CC exhibits preeminent performance for the HER. Specifically, it only requires an overpotential of 85 mV to achieve a current density of 10 mA cm-2 in 1.0 M KOH solution. Moreover, the V-Ni2P NSAs/CC shows superior electrochemical stability, maintaining its HER performance up to 3000 cyclic voltammetry cycles. This work affords a guiding strategy for the synthesis of a high-performance and stable electrocatalyst for the HER.

N-doping nanoporous carbon microspheres derived from MOFs for highly efficient removal of formaldehyde.

Indoor formaldehyde (HCHO) removal is very important to reduce public health risk. Herein, we report a facile method for preparing N-doped nanoporous carbon through direct carbonization of metal-organic frameworks (ZIF-8) to remove harmful formaldehyde. The prepared N-doped nanoporous carbon exhibited uniform morphology and large specific surface area. Moreover, the type of N-functional groups on the N-doped nanoporous carbon had a dominant effect on its HCHO adsorption activity. As a result, HCHO adsorption capacity of the optimized N-doped nanoporous carbon was approximately five times higher than that of the commercially activated carbon. The detailed HCHO adsorption process, including physical adsorption and chemical adsorption, was also confirmed through in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). In addition, it should be noted that the N-doped nanoporous carbon exhibited high stability for HCHO adsorption, even after six adsorption cycles, indicating its good recyclability for long-term application. This study is expected to pave a way for expanding the environmental applications of the N-doped nanoporous carbon.

MnMoO4 nanosheet array: an efficient electrocatalyst for hydrogen evolution reaction with enhanced activity over a wide pH range.

We report the preparation of MnMoO4 nanosheet array on nickel foam (MnMoO4 NSA/NF) as an excellent 3D hydrogen evolution reaction (HER) electrocatalyst with good catalytic performance applied under basic, acidic and neutral conditions. In 0.5 M H2SO4, this MnMoO4 NSA/NF electrode needs an overpotential of 89 mV to drive current densities of 10 mA cm-2, to achieve the same current density, it demands overpotentials of 105 mV in 1.0 M KOH, 161 mV in 1.0 M PBS (pH = 7), respectively. After continuous CV scanning for 1000 cycles under different pH conditions, it also demonstrates an excellent stability with ignorable activity decrease. Such preeminent HER performance may be derived from the synergistic effect between manganese (Mn) and molybdenum (Mo) atoms, exposure of more active sites on the nanosheets and effective electron transport along the nanosheets. This MnMoO4 NSA/NF electrocatalyst provides us a highly efficient material for water splitting devices for industrial hydrogen production.