Search Results (29)

This study investigates how phospholipid headgroups influence passive membrane penetration and structural impact of four nitrogen-, sulfur-, and oxygen-containing heterocycles (NSO-HETs)—N-methyl-2-pyrrolidone (PIR), 1,4-dioxane (DIOX), oxane (OXA), and phenol (PHE). Using all-atom molecular dynamics simulations combined with Accelerated Weight Histogram free energy calculations, the passive transport of NSO-HETs across DPPC, DPPE, DPPA, and DPPG bilayers was characterized. DPPG showed the highest membrane affinity, increasing permeability (logP_memb/bulk) by 27–64% compared to DPPE, associated with the lowest permeability and tightest lipid packing. Free energy barriers are also decreased in DPPG relative to DPPE; PIR’s central barrier dropped from 19.2 kJ/mol (DPPE) to 16.6 kJ/mol (DPPG), while DIOX’s barrier decreased from 7.2 to 5.2 kJ/mol. OXA exhibited the lowest central barriers (1.2–2.2 kJ/mol) and uniquely accumulated at higher concentrations in the bilayer center than in bulk water, with free energy ranging from −3.4 to −5.9 kJ/mol. PHE and OXA caused significant bilayer thinning (up to 11%) and reduced lipid tail order, especially in DPPE and DPPA. Concentration effects were most pronounced in DPPE, where high solute loading disrupted lipid order and altered free energy profiles. These results highlight the crucial role of headgroup identity in modulating NSO-HET membrane permeability and structural changes. Full article

Selective catalytic reduction filter (SDPF) technology constitutes a critical methodology for controlling nitrogen oxide (NOx) and particulate matter emissions from light-duty diesel vehicles. A series of SDPFs with different sulfur poisoning times and concentrations were prepared using the worldwide harmonized light vehicles test cycle (WLTC). Bench testing revealed that sulfur poisoning diminished the catalyst’s NH₃ storage capacity, impaired the transient NOx reduction efficiency, and induced premature ammonia leakage. After multiple sulfur poisoning incidents, the NOx reduction performance stabilized. Higher SO₂ concentrations accelerated catalyst deactivation and hastened the attainment of this equilibrium state. The characterization results for the catalyst indicate that the catalyst accumulated the same sulfur content after tail gas poisoning with different sulfur concentrations and that sulfur existed in the form of SO₄²⁻. The sulfur species in low-sulfur-poisoning-concentration catalysts mainly included sulfur ammonia and sulfur copper species, while high-sulfur-poisoning-concentration catalysts contained a higher proportion of sulfur copper species. Neither species type significantly altered the zeolite coating’s crystalline structure. Sulfur ammonia species could easily lead to a significant decrease in the specific surface area of the catalyst, which could be decomposed at 500 °C to achieve NOx reduction performance regeneration. In contrast, sulfur copper species required higher decomposition temperatures (600 °C), achieving only partial regeneration. Full article

When iron sulfides are used as aggregate in concrete production, it easily oxidizes to form harmful substances such as sulfates. This results in acid corrosion and internal sulfate attack (ISA), significantly reducing concrete durability. To date, the quantification methods for iron sulfides in aggregates remain inaccurate, often neglecting pyrrhotite (a type of iron sulfide). No standardized methods or threshold values for the sulfide content in aggregates have been established, nor have technical guidelines for the application of sulfide-containing aggregates, limiting their use. This study proposes an on-site quantification procedure for determining the pyrite and pyrrhotite content in tailings using a selective chemical dissolution process. An orthogonal experiment was designed to determine the optimal dissolution conditions by considering four factors: particle size, reaction temperature, acid concentration, and reaction time. The pyrrhotite quantification method showed a relative standard deviation (RSD) of 3.60% (<5%) and a mean relative error of 3.19% (<5%), while the pyrite quantification method showed an RSD of 3.11% (<5%) with a mean relative error of 4.70% (<5%). The results were further optimized under engineering conditions to reduce costs and enable on-site quantification without relying on complex precision instruments. The quantitative results of pyrite in mineral samples were verified by the XRD internal standard method, and the error was less than 0.6%. This approach ensures the effective monitoring and management of sulfide content in concrete aggregates, promoting the practical application of sulfur-bearing aggregates. Full article

Autogenously calcined clays from tailings dumps, which are formed by the ignition of the contained residual coal, represent a huge resource of potentially pozzolanic material worldwide. This work presents preliminary studies of samples from the Western coal regions in Germany and investigations on the first industrially produced cement with autogenously calcined tailings concerning its suitability as supplementary cementitious material (SCM). Samples of the tailings materials and blended cements were thoroughly characterized physically, chemically and mineralogically. The reactivity was studied using the R³ test and mortar compressive strength testing. The influence on cement hydration was studied using X-ray diffractometry (XRD) and isothermal calorimetry. The preliminary investigations showed that the material is basically suitable as SCM, as it consists mainly of SiO₂ and Al₂O₃, which partially occurs in X-ray amorphous form and has a low content of impurities, which can impair cement properties such as carbon or sulfur. The R³ reactivity and the relative compressive strength differed significantly depending on the sample. For the industrial cement production trial, low-processed material was used which still contained inert fractions. The average sample showed a relatively low R³ reactivity but still significantly higher than mostly inert materials such as limestone or quartz powder. Calorimetry and XRD investigations on cement pastes showed that the clinker reactions remain basically unaffected by the tailings. Mortar tests showed that the material contributes to strength development at a late age. It can be concluded that the tailings are basically suitable as SCM and, in appropriate blends, the clinker factor and, thus, the CO₂ footprint of cement can be reduced. Full article

Against the backdrop of the increasing copper demand in a low-carbon economy, this work statistically forecasted the distribution of China’s copper tailings for the first time, and then characterized them as finely crushed and low-grade mining solid wastes containing copper mainly in the form of chalcopyrite, bornite, covelline, enargite and chalcocite based on available research data. China is the globally leading refined copper producer and consumer, where the typical commercial-scale bioleaching of copper tailings is conducted in the Dexing, Zijinshan and Jinchuan mining regions. And these leaching processes were compared in this study. Widely used chemolithoautotrophic and mesophilic bacteria are Acidithiobacillus, Leptospirillum, Acidiphilium, Alicyclobacillus and Thiobacillus with varied metal resistance. They can be used to treat copper sulfide tailings such as pyrite, chalcopyrite, enargite, chalcocite, bornite and covellite under sufficient dissolved oxygen from 1.5 to 4.1 mg/L and pH values ranging from 0.5 to 7.2. Moderate thermophiles (Acidithiobacillus caldus, Acidimicrobium, Acidiplasma, Ferroplasma and Sulfobacillus) and extreme thermophilic archaea (Acidianus, Metallosphaera, Sulfurococcus and Sulfolobus) are dominant in leaching systems with operating temperatures higher than 40 °C. However, these species are vulnerable to high pulp density and heavy metals. Heterotrophic Acidiphilium multivorum, Ferrimicrobium, Thermoplasma and fungi use organic carbon as energy to treat copper oxides (malachite, chrysocolla and azurite) and weathered sulfides (bornite, chalcocite, digenite and covellite) under a wide pH range and high pulp density. We also compared autotrophs in a planktonic state or biofilm to treat different metal sulfides using various sulfur-cycling enzymes involved in the polysulfide or thiosulfate pathways against fungi that produce various organic acids to chelate copper from oxides. Finally, we recommended a bioinformatic analysis of functional genes involved in Fe/S oxidization and C/N metabolism, as well as advanced representation that can create new possibilities for the development of high-efficiency leaching microorganisms and insight into the mechanisms of bioleaching desired metals from complex and low-grade copper tailings. Full article

Cobalt is a critical metal widely distributed in nature, but cobalt ore has hardly been found as an independent mineral. Cobalt-bearing pyrite tailings separated from iron ore is one of the resources for recovering cobalt. In the following study, roasting is carried out to oxidize cobalt-bearing pyrite tailings for preparing and recovering the cobalt by acid leaching. The further aim of the research is to determine and control the optimal technological regime for roasting by using thermodynamic modeling. The phase transition in Fe–S–O and Co–S–O systems and its mechanism are analyzed under the partial pressure of oxygen and sulfur dioxide at constant temperatures. Thermodynamic modeling proves that iron and cobalt sulfides can be intensively oxidized at a relatively high temperature (>900 °C) under an atmosphere of logp(O₂) > −5, leading to the formation of SO₂ (logp(SO₂) < 0). The results of the roasting experiment indicate 98% desulfurization degree upon holding for about 4–5 h and at > 1000 °C. Based on these thermodynamic modeling and experimental results, the roasting of cobalt containing pyrite can be optimized with substantial productivity with regard to the metal oxide and cobalt thereof. Oxidative roasting also allows the elimination of environmentally hazardous gases such as sulfur during the process. Full article

In this study, 50% iron ore tailings (IOTs) were used to prepare the cemented mortar at low economic costs and with great environmental benefits. Basalt fiber (BF) and polyacrylonitrile fiber (PANF) were added to the tailing mortar to improve the comprehensive performance of tailing mortars, including BF (0~0.5%), PANF (0~0.05%) and the combination of them. The results show that the addition of BF and PANF can significantly improve the ultrasonic velocity, uniaxial compressive strength (UCS), split-tensile strength (STS), flexural strength (FS) and toughness of the tailing mortar. A novel finding is that the enhancement of hybrid fibers is much better than single fiber, and the best hybrid fiber combination is B0.25P0.05 (0.25 wt% BF and 0.05 wt% PANF), because this combination not only causes the most considerable increase in strength but also possesses great cost-effectiveness. Compared to the B0P0 group without fibers, the maximum increments of B0.25P0.05 in UCS, STS and FS are 45.74%, 52.33% and 15.65%, respectively. It is evidenced that the improvement in STS is the largest because the fibers have good cracking resistance and bridging effect in the tailing mortar. The scanning electron microscope (SEM) further confirms that too many hybrid fibers will agglomerate and produce more voids, which is harmful to the development of the internal structure. Beyond B0.25P0.05, the hydration products are also reduced due to the decrease in nucleation sites, observed by combining X-ray diffraction (XRD) tests. Therefore, it is suggested that the hybrid fibers containing 0.25% BF and 0.05% PANF should be used in this tailing mortar. Full article

Odorous sediments containing volatile organic sulfur compounds (VOSCs) are a common issue in shallow water reservoirs globally. Volatile organic sulfur compounds are a typical class of malodorous substances that have attracted widespread attention due to their pungent odors and extremely low odor thresholds. The insufficient hydrodynamic conditions in the reservoir area lead to the accumulation of pollutants in the sediment, where biochemical reactions occur at the sediment–water interface, serving as a significant source of foul-smelling substances in the water body. This study analyzed sediment samples from 10 locations across a shallow water reservoir using flavor profile analysis, an electronic nose, and gas chromatography-mass spectrometry. The predominant odor types were earthy/musty and putrid/septic, with key odorants being VOSCs, 2-methylisoborneol, and geosmin. The results revealed VOSCs from organic matter account for up to 96.7% of odor activity. More importantly, concentrations and release fluxes of VOSCs consistently decrease along the water flow direction from dam regions to tail regions. This trend matches organic matter accumulation patterns in shallow reservoirs and highlights dam areas as hotspots for malodorous sediment. The generalized spatial distribution pattern and identification of key malodorous compounds establish a basis for understanding and managing odor issues in shallow freshwater reservoir sediments. Full article

Super-hot acid leach residue is generated during zinc production in the roasting–leaching–electrowinning route, where both primary and secondary resources are used as feed material. This residue may contain valuable metals, such as lead, zinc, and iron, as well as precious metals, such as gold and silver. Four materials, namely super-hot acid leach residue, a residue formed when super-hot acid leach residue is selectively leached for lead with triethylenetetramine, as well as flotation concentrate, and flotation tailings formed in a selective silver flotation process with super-hot acid leach residue as the feed material were characterized to obtain a deeper understanding of possible further metal extraction. These four materials were characterized for chemical composition, mineralogy, and mineral distribution via chemical analyses, X-ray diffraction, and energy-dispersive scanning electron microscopy, respectively. The scanning electron microscope images showed that the materials have large variations in particle size distribution and composition. The results showed that the main lead phase in super-hot acid leach residue is lead sulfate, whereas it is mostly converted to lead sulfide during the selective lead leaching of the super-hot acid leach residue. The remaining lead sulfate is found in a solid solution with barium sulfate. Extracting lead from super-hot acid leach residue via triethylenetetramine leaching resulted in increased concentrations of gold and silver by 41% and 42%, respectively. The identified silver phases in super-hot acid leach residue may correspond to silver sulfide, silver chloride, and elementary silver, where silver sulfide was the most commonly occurring silver phase. After leaching this selectively for lead with triethylenetetramine, similar silver phases were identified, but silver sulfide and silver chloride occurred to a similar extent. Additionally, silver copper sulfide was detected. The presence of different silver phases might pose a challenge to reaching high silver recovery during leaching as the optimum leaching conditions differ somewhat. Furthermore, elemental sulfur, with a tendency to coat gold and silver particle surfaces, which is indicated to be present in all materials except the silver flotation tailings, may hinder metal extraction. Full article

This study presents the results of the enlarged laboratory research on the melting of calcined composite pellets for ferrochrome obtained from fine-dispersed conditioned chrome concentrate containing 50.3% Cr₂O₃. This is a product of the gravitational beneficiation of waste sludge tailings from the Dubersay tailings dump at the Donskoy Mining and Processing Plant (DMPP) of JSC “TNC Kazchrome”. The composition of the charge for obtaining composite pellets consisted of 88.5% of chrome concentrate, 3% of mineral part of refined ferrochrome slag (RFC), 4% of ferruginous diatomite, 3% of coke and 1.5% of liquid glass. The initial charge was pelletized on a laboratory pelletizer to a size of 6–10 mm, dried at room temperature for 24 h and fired at 1200 °C for 60 min at a heating rate of 15 deg/min. On the basis of the developed composite annealed pellets, studies on the production of high-carbon ferrochrome at different melting temperatures were carried out. The results showed that with an increase in temperature from 1750 to 1850 °C, the iron–chromium phase in the composition of the alloy increases from 45.2 to 50.1%, the chromium carbide phase decreases from 23.7 to 11.3% and the chromium–iron phase increases from 7 to 11.2%. The carbon content in the alloys at temperatures from 1750 to 1850 °C varies from 7.2 to 8.94%, respectively. The maximum chromium content of the alloy is 64.82% with a melting point of 1850 °C; this alloy can be classified as FeCr60C90LP grade ferrochrome according to the international Chinese standard, which has no more than 0.03% phosphorus and no more than 0.1% sulfur. Full article

Combretastatin derivatives is a promising class of antitumor agents, tubulin assembly inhibitors. However, due to poor solubility and insufficient selectivity to tumor cells, we believe, their therapeutic potential has not been fully realized yet. This paper describes polymeric micelles based on chitosan (a polycation that causes pH and thermosensitivity of micelles) and fatty acids (stearic, lipoic, oleic and mercaptoundecanoic), which were used as a carrier for a range of combretastatin derivatives and reference organic compounds, demonstrating otherwise impossible delivery to tumor cells, at the same time substantially reduced penetration into normal cells. Polymers containing sulfur atoms in hydrophobic tails form micelles with a zeta potential of about 30 mV, which increases to 40–45 mV when cytostatics are loaded. Polymers with tails of oleic and stearic acids form poorly charged micelles. The use of polymeric 400 nm micelles provides the dissolution of hydrophobic potential drug molecules. Micelles could significantly increase the selectivity of cytostatics against tumors, which has been shown using MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay, Fourier transform infrared (FTIR) spectroscopy, flow cytometry and fluorescence microscopy. Atomic force microscopy presented the difference between the unloaded micelles and those loaded with the drug: the size of the former was 30 nm on average, while the latter had a “disc-like” shape and a size of about 450 nm. The loading of drugs into the core of micelles was confirmed by UV and fluorescence spectroscopy methods; shifts of absorption and emission maxima into the long-wavelength region by tens of nm was observed. With FTIR spectroscopy, a high interaction efficiency of micelles with the drug on cells was demonstrated, but at the same time, selective absorption was observed: micellar cytostatics penetrate into A549 cancer cells 1.5–2 times better than the simple form of the drugs. Moreover, in normal HEK293T, the penetration of the drug is reduced. The proposed mechanism for reducing the accumulation of drugs in normal cells is the adsorption of micelles on the cell surface and the preservation of cytostatics to penetrate inside the cells. At the same time, in cancer cells, due to the structural features of the micelles, they penetrate inside, merging with the membrane and releasing the drug by pH- and glutathione-sensitive mechanisms. From a methodological point of view, we have proposed a powerful approach to the observation of micelles using a flow cytometer, which, in addition, allows us to quantify the cells that have absorbed/adsorbed cytostatic fluorophore and distinguish between specific and non-specific binding. Thus, we present polymeric micelles as drug delivery systems in tumors using the example of combretastatin derivatives and model fluorophore-cytostatic rhodamine 6G. Full article

Prolonged development of ore deposits, ore beneficiation and metallurgical smelting of concentrates result in the accumulation of wastes, forming large-scale dumps and sludge ponds negatively affecting the environment and human health. The creation and introduction of industrial waste treatment technologies will make it possible to dispose of them with the production of valuable commercial products and improve the environmental situation. In a research article on chemical beneficiation with the subsequent gravitational beneficiation of chrome-containing slurry tailings of Donskoy Ore-Mining and Beneficiation Plant (DOMBP), which processes chrome ore of the Kempirsay deposit in the Republic of Kazakhstan, Aktobe region, having considerable stocks of such waste is presented. The chromium-containing slurry tailings were heat-treated at 1100 °C, sintered with ammonium sulfate, water and sulfuric acid in a defined ratio at 300 °C, and then the resulting sinter was leached with water at 90 °C. The cake was washed to separate the liquid part from the solid part. The solid precipitate is the chromium-containing cake, which is upgraded by gravity concentration to a grade concentrate for ferroalloy production. When the solution is evaporated, magnesium sulfate with ammonium sulfate forms the Tutton’s salt ammoshenite. High-throughput chromium oxide extraction of 93.9% was achieved as a result of the research, and three products were obtained: (1) standard chromium concentrate with 49.48% Cr₂O₃ content, (2) ammoshenite used as a nitrogen–magnesium fertilizer and (3) forsterite, which is concentrated in gravity concentration tailings and can be used in the production of refractory minerals. Full article

Sulfur-containing amino acids methionine (Met), cysteine (Cys) and taurine (Tau) are common dietary constituents with important cellular roles. Met restriction is already known to exert in vivo anticancer activity. However, since Met is a precursor of Cys and Cys produces Tau, the role of Cys and Tau in the anticancer activity of Met-restricted diets is poorly understood. In this work, we screened the in vivo anticancer activity of several Met-deficient artificial diets supplemented with Cys, Tau or both. Diet B1 (6% casein, 2.5% leucine, 0.2% Cys and 1% lipids) and diet B2B (6% casein, 5% glutamine, 2.5% leucine, 0.2% Tau and 1% lipids) showed the highest activity and were selected for further studies. Both diets induced marked anticancer activity in two animal models of metastatic colon cancer, which were established by injecting CT26.WT murine colon cancer cells in the tail vein or peritoneum of immunocompetent BALB/cAnNRj mice. Diets B1 and B2B also increased survival of mice with disseminated ovarian cancer (intraperitoneal ID8 Tp53^−/− cells in C57BL/6JRj mice) and renal cell carcinoma (intraperitoneal Renca cells in BALB/cAnNRj mice). The high activity of diet B1 in mice with metastatic colon cancer may be useful in colon cancer therapy. Full article

In order to achieve efficient resource utilization of metal tailings, taking the roasted clinker of silver tailings (RCST) as the object, the dissolution behaviors of Si, Al and Fe in the water–acid two-stage leaching process and the water leaching kinetics of Si were investigated in this study. Single-factor experiments were performed to investigate the effects of the leaching parameters; the XRF, XRD and SEM-EDS methods were used to characterize the leaching residues with different leaching times, and the leaching kinetics models of Si were established. The results demonstrate that, in the water leaching stage, the sodium silicate and a small part of the structurally unstable sodium aluminosilicate in RCST are dissolved, while the nepheline, most of the sodium aluminosilicate and the mixed materials containing iron enter the water leaching residue. The first 5 min of water leaching is controlled by both interfacial transfer and diffusion across the product layer, with an apparent activation energy of 22.36 kJ/mol, and the dissolution reaction during 5–15 min is controlled by the unsteady diffusion of the liquid film, with an apparent activation energy of 14.22 kJ/mol. The structure of the materials in the clinker is completely destroyed, and a great number of fissures and pores are produced by the continued dissolving action of the water. Thus, in the acid leaching stage, the amorphous Si-, Al- and Fe-containing substances in the water leaching residue are rapidly dissolved in the sulfuric acid solution at a lower temperature. Full article

With the vigorous development of the world’s mineral resources, the global ecological environment has been severely damaged. The tailings cemented filling technology is an important way to realize the green and low-carbon development of the mining industry. However, sulfur-containing tailings from metal mines can destroy the stability and strength of cemented tailings backfill. Therefore, it is imperative to reduce the harm of the sulfur-containing tailings to the strength of cemented tailings backfill. Firstly, based on the research results of sulfur-containing tailings cemented backfill in recent years, this paper reviews the influence of sulfur-containing tailings on the strength of cemented backfill. Accordingly, the mechanism of strength failure of cemented backfill caused by sulfur-containing tailings is further studied, and the erosion failure of sulfide and sulfate is deeply discussed and analyzed. In addition, three control measures are proposed, including adjusting the combination of filling materials and optimizing the filling ratio, controlling the oxidation conditions in the filling process, and adding ad-mixtures as a supplement. Finally, the main conclusions and outlooks of this review are summarized. The purpose of this review is to provide guidance to improve the strength and durability of the cemented sulfur tailings backfill, effectively treating metal tailings, and to propose some ideas for the further improvement and development of the tailings cemented filling technology. Full article