Degree Of Mineralization Research Articles

The Electrooxidation of Synthetic Bipyridyl Herbicide Wastewaters with Boron-Doped Diamond Electrodes: A Technical and Economic Study to Boost Their Application for Pollution Prevention in the Agricultural Sector

Boron-doped diamond electrodes (BDDEs) offer a highly efficient pathway to mineralize recalcitrant compounds due to their reduced energy requirements, fewer chemical inputs, and mechanical stability. In this work, the electrochemical degradation of paraquat (PQ) and diquat (DQ) was studied using an undivided cell (Condiacell®-type) at circumneutral pH, and under galvanostatic control. The roles of applied current density, volumetric flow rate, and herbicide concentration were systematically studied through a central composite design (CCD) using a closed-flow reaction setup. Under the best operating conditions (i.e., for PQ: 1.6 mA/cm2, 80 mL/min, and 70 mL/min, and 70 mg/L; and for DQ: 1.5 mA/cm2, 80 mL/min, and 73 mg/L), a spectrophotometric analysis evidenced that the herbicides were satisfactorily removed (ca. 100%) while mineralization degrees were above 90%. Furthermore, the produced effluents yielded significant increases in seed germination and root length, which suggest a reduction in toxicity. Energy consumptions of 0.13 and 0.18 kWh/g of TOC are reported with the electrochemical cells for the PQ and DQ treatments, respectively. The PQ and DQ treatments by electrooxidation are estimated to emit nearly 2.7 and 38.9 kg CO2/m3 of water treated, with a cost around USD 250/m3. Carbon emissions could be greatly decreased for PQ (0.28 kg CO2/m3) and DQ (0.40 kg CO2/m3) if electricity were generated from renewable resources. Although this study suggests that the use of BDDE can be considered as a green alternative for agrochemical removal due to lower carbon emissions, the environmental profile of the process is determined by the degree of renewability of the electrical grid of each country or region.

Toxicological and environmental risks of enalapril and their possible transformation products generated under phototransformation reactions

Pharmaceutical active compounds (PACs) in the concentration range of hundreds of ng/L to μg/L have been identified in urban surface water, groundwater, and agricultural land where they cause various health risks. These pollutants are classified as emerging and cannot be efficiently removed by conventional wastewater treatment processes. The use of nano-enabled photocatalysts in the removal of pharmaceuticals in aquatic systems has recently received research attention owing to their enhanced properties and effectiveness. In the current study, toxicological and environmental risks of enalapril (ENL) and their possible transformation products (TPs) generated under phototransformation processes (e.g., photolysis and photocatalysis reactions) were assessed. In photolysis reaction, removal of ENL was incomplete (< 16%), while mineralization degree was negligible. In contrast, total removal of ENL was achieved through the photocatalytic process and its maximum mineralization ratio was 66% by using natural radiation. Proposed transformation pathways during the phototransformation of ENL include hydroxylation and fragmentation reactions generating transformation products (TPs) such as hydroxylated TPs (m/z 393) and enalaprilat (m/z 349). Potential environmental risks for aquatic organisms were not observed in the concentrations of both ENL and enalaprilat contained in surface water. However, the acute and chronic toxicities prediction of TPs such as m/z 409, 363, and 345 showed toxic effects on aquatic organisms. Thus, more studies regarding TPs monitoring for both ENL and PhACs with highest occurrence worldwide are necessary for the creation of a database of the concentrations contained in surface water and groundwater for the assessment of the potential environmental risk for aquatic organisms.

Piezoelectric-enhanced MoS2@PVDF-HFP composite for photocatalytic degradation of tetracycline

In this work, composite films of molybdenum disulfide (MoS2) with poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) were fabricated using aqueous phase transformation and hydrothermal methods, aiming at efficiently degrading tetracycline hydrochloride (TC). The findings revealed that the degradation efficiency of TC by MoS2@PVDF-HFP, when subjected to a combined photocatalysis process involving a simulated pressure electric field and aeration, reached a remarkable 96.11% within 1 hour-surpassing the performance observed under individual conditions. The changes in the electron density cloud on the films surface induced by the pressure electric field and the acceleration of electron transfer rate between contact interfaces were evident. Notably, the composite films exhibited a stable performance with a TC removal rate of 90.23% after five cycles, including a relatively stable degree of mineralization. We employed Density Functional Theory (DFT) to investigate the changes in the state density of MoS2@PVDF-HFP under different conditions, such as compressive stress, tension, and no force. This further clarified the mechanism of piezoelectric coupling photocatalysis promoting induced charge transfer on the films surface. The research findings presented in this paper provide a promising avenue for the application of piezoelectric field-assisted photocatalysis in enhancing material performance.

Optimized Methyl methacrylate embedding of small and large undecalcified bones.

Methyl methacrylate (MMA) plastic embedding has been long established as a technique for the processing and histological assessment of bones. It provides the added benefit over paraffin in that it does not require decalcification of the tissue in order visualize the cellular detail, thus preserving vital information about the amount of unmineralized osteoid present in addition to the degree of mineralization in the bone. It also allows for the incorporation of dynamic histomorphometric analysis through the retention of fluorescent labels incorporated into the bone. Efficient infiltration of hard tissue is essential to the processing of bones and producing quality slides suitable for achieving usable quantifiable histology out the other end. This technique:• Updates previously published MMA embedding protocols to reflect utilization of stabilized acrylamides (over the unstabilized reagents of the past)• Outlines the techniques that are important for embedding both small (mus), medium (rattus), and large (porcine, lagomorph, human) histological samples.• Updates the clearing and infiltration processes utilized and validates quality of the sample preparation though histological staining to confirm preservation of cellular detail, mineralization information, and enzymatic activity

Coal Wetting Characteristics and Mechanism of Water with Different Degrees of Mineralization

Coal Wetting Characteristics and Mechanism of Water with Different Degrees of Mineralization

Experimental Investigation of the Influence of Composition Changes in Shale on Pore Structure and Fractal Characteristics under Different HCl Concentrations.

Acidification is a promising stimulation technique for improving the pore structure of low-permeability shale reservoirs and enhancing shale gas production. Variations in the mineral composition and acid concentration play a significant role in altering the pore systems in shale reservoirs, thereby affecting shale gas transport and production. To investigate the effect of shale composition on pore structure and fractal characteristics under hydrochloric acid (HCl) treatment, experiments were carried out on carbonate-rich (68%), carbonate-medium (45%), and carbonate-poor (2%) shales with different concentrations of HCl solution (1, 5, 10 wt %). X-ray diffraction (XRD), low-temperature nitrogen adsorption, and fractal theory were performed to investigate variations in mineral composition, pore structure, and fractal characteristics of the unreacted and reacted shales. The results illustrated that the HCl treatment significantly reduced the content of carbonate minerals, and the dissolution degree of carbonate minerals increased with the increase in HCl concentration. More meso- and macropores were generated for carbonate-rich and carbonate-medium shale, while more micro- and mesopores were generated in carbonate-poor shale, which led to the increase in total pore volume (TPV) and total specific surface area (TSSA) at different degrees. Moreover, the pore surface roughness (D 1) and structure complexity (D 2) were reduced with the increase of HCl concentration for carbonate-rich shale, while the alteration of D 1 and D 2 showed an opposite trend for carbonate-poor shale. Additionally, D 1 decreased and D 2 increased for carbonate-medium shale. Relevant results could provide theoretical references for the acid fracturing of shale reservoirs with varying mineral compositions.

MiR-21-5p Promotes Osteogenic Differentiation and Calcification of Valvular Interstitial Cells by Targeting TGFBI in Calcific Aortic Valve Disease.

Calcific aortic valve disease (CAVD) is the most common heart relating disease with high morbidity and mortality, especially in elderly population. While extensive investigations have been devoted to the study of mechanistic pathways related to CAVD, the key factors and mechanisms mediating valve mineralization remain unclear. The aim of this study is to investigate the role of mirnas and their downstream targets in CAVD disease progression. A previous recent multi-omics study suggested a novel CAVD molecular interaction network contained miR-21-5p. CAV and their pair-matched adjacent normal tissues were obtained from 15 patients pathologically diagnosed as CAVD and admitted in Yancheng Third People's Hospital (The Sixth Affiliated Hospital of Nantong University) from 2019-2021. RT-qPCR was utilized for detection of miR-21-5p and related protein expression levels to confirm the related factors in CAVD progression. Western blotting was applied to strengthen the results of RT-qPCR and confirm osteogenic differentiation of VICs via biomarker detection. The staining of alkaline phosphatase (ALP) and alizarin red was performed to assess the degree of VIC mineralization. We found that miR-21-5p was remarkably increased (P<0.0001) in calcified aortic valves (AVs) whereas TGFBI was diminished (P<0.01) in CAVD samples compared to the paired normal tissues from CAVD patients. Additionally, TGFBI was targeted by miR-21-5p. Furthermore, overexpressing TGFBI could block VIC osteogenic differentiation mediated by miR-21-5p. To sum up, miR-21-5p promotes VIC osteogenic differentiation and calcification via TGFBI in CAVD progression. Our work might bring a sight on underlying mechanisms of CAVD progression and provide a possible therapeutic target for diagnosis and treatment.

Kinetic characteristics of bornite and chalcopyrite dissolution in nitric acid

The kinetic characteristics of dissolution of copper-bearing sulfides – chalcopyrite (CuFeS₂) and bornite (Cu₅FeS₄) – in nitric acid were studied. The kinetics of the dissolution process was described using a compressible nucleus model. Chalcopyrite of the Vorontsovskoye deposit and bornite of the Karabash deposit were used as research objects. Solution and cake samples were analyzed by optical emission spectrometry and X-ray fluorescence analysis, respectively. The results obtained were processed in the MS Excel software package. The influence of various factors, including temperature, solvent concentration, particle size, and process duration on the dissolution degree of minerals was studied. The process parameters were varied as follows: temperature – from 35 to 95°C; HNO₃ concentration – from 1 to 9 mol/dm³; particle size – from +0.1 to 0.056 mm; duration – from 0 to 60 min. It was established that an increase in temperature and acid concentration leads to a significant increase in the degree of dissolution of both chalcopyrite and bornite. A decrease in particle size also contributes to a more efficient dissolution of both minerals in nitric acid. The calculated activation energy values were 55 kJ/mol for chalcopyrite and 43 kJ/mol for bornite, which is characteristic of the kinetic region of the process. The reaction orders in terms of reactant were determined: 1.62 for chalcopyrite and 1.57 for bornite. In terms of particle size, these were -1.16 for chalcopyrite and -2.53 for bornite. On this basis, generalized equations of dissolution kinetics for both minerals were derived. The results obtained allow an assumption about the kinetic nature of dissolution of chalcopyrite and bornite under the studied conditions.

Application of the Raman fluorescence method to study the effects of chemical, physical and radiation factors on the mineralization of hard dental tissues

Objective. To study the effect of physical, chemical and radiation factors on the degree of mineralization of the hard dental tissues surface using spectroscopy. Materials and methods. The degree of mineralization of hard dental tissues was studied by the Raman spectroscopy using hardware-software complex InSpectrum M on the teeth removed according to clinical indications (in vitro): in varying degrees of moisture (dry and wet); before and after exposure to acid and remineralizing drug; before and after exposure to radiation Results. The data obtained demonstrated the difference in the indicators in dry (1801 [1800; 1802]) relative units, and moistened (591.5 [591; 592]) teeth. The mineralization of teeth according to Raman Intensity before exposure to citric acid, was (602 [601; 602]) rel. units, and after the exposure it was (152 [152; 153]) rel. units, after application of the cm-2 plate it was (423 [422; 423]) rel. units. The identified differences are reliable (p 0.001). Thus, it is confirmed that organic acids (citric acid) contribute to the enamel demineralization by more than two times, and the use of calcium-containing plates contributes to remineralization almost to the initial state. At the same time, there were no significant differences in the level of mineralization (according to the Raman method of fluorescence spectroscopy) in teeth before and after direct radiation exposure, regardless of dose (2 Gy, 70 Gy, 110 Gy) in any of the functional groups (incisors, canines, premolars, molars). Conclusions. 1. Raman-fluorescence spectroscopy has a high sensitivity and is capable of detecting mineralization, de- and re-mineralization of hard dental tissues. 2. It is recommended to determine the hard tooth tissues mineralization by Raman-fluorescence spectroscopy in a moistened rather than a dry form. 3. Organic acids contribute to the demineralization of enamel, and the use of calcium-containing plates promotes its remineralization. 4. Direct radiation exposure does not have a direct effect on the mineralization of the surface of the hard dental tissues. regardless of the dose applied in all functional groups (incisors, canines, premolars, molars), in all areas of the teeth (equator, cutting edge, gum border).

Proanthocyanidins modification of the mineralized collagen scaffold based on synchronous self-assembly/mineralization for bone regeneration

Proteoglycans (PG) is crucial for regulating collagen formation and mineralization during bone tissue development. A wide variety of PG-modified collagen scaffolds have been proposed for bone engineering application to promote biological responses and work as artificial matrices that guide tissue regeneration. However, poor performance of theses biomaterials against infections has led to an unmet need for clinical prevention. Therefore, we utilized proanthocyanidins (PA) to simulate the functions of PG, including mediating the collagen assembly and intrafibrillar mineralization, to optimize scaffolds performance. The excellent antibacterial properties of PA can endow the scaffolds with anti-infection effects in the process of tissue regeneration. When PA was added during fibrillogenesis, the collagen fibrils appeared irregular aggregation and the mineralization degree was reduced. In contrast, the addition of PA after collagen self-assembly improved the latter’s ability to act as a deposition template and remarkably promoted mineral ions infiltration, thus enhancing intrafibrillar mineralization. The PA-modified scaffold displayed a highly hydrophilicity behaviour and long-term resistance to degradation. The sustained release of PA effectively inhibited the activity of Staphylococcus aureus. The scaffold also showed excellent biocompatibility and improved bone regeneration in calvarial critical-size defect models. The application of PA enables a dual-function scaffold with favourable intrafibrillar mineralization and anti-bacterial properties for bone regeneration.

Melamine enhancing Cu-Fenton reaction for degradation of anthracyclines

Melamine (MA) enhanced Cu-Fenton process was developed for the degradation of anthracyclines. Taking daunorubicin (DNR) degradation as an example, we found that the initial first-order apparent constant of Cu2+/MA/H2O2 system with a molar ratio of 1:8 for Cu2+:MA was 5.2 times higher than that of conventional Cu2+/H2O2 system. The in-situ reductive coordination between Cu2+ and MA facilitated the generation and stabilization of Cu+ species, thereby accelerating the rate-limiting step of Cu2+/Cu+ conversion and maintaining high levels of Cu+ during the degradation process. Moreover, pre-synthesized Cu+-MA complexes (e.g., CM-250) further enhanced the efficiency of the Cu-Fenton reaction by increasing both the Cu+ proportion and MA chelation. The apparent activation energy for DNR degradation in CM-250 mediated Fenton reaction (15.9 kJ mol−1) was lower than that in systems involving Cu2+/MA (41.2 kJ mol−1) and Cu2+ (65.6 kJ mol−1). Enhanced generation of various reactive oxygen species (·OH,·O2-, and 1O2) was confirmed, with 1O2 playing a dominant role, significantly improving both degradation rate and mineralization degree for DNR. MA-enhanced Cu-Fenton process also offers a convenient alternative to effectively remove other anthracyclines and organic micropollutants, holding great promise for advancing advanced oxidation processes as well as practical large-scale degradation applications targeting multiple pollutants.

Manganese oxidation states and availability in forest weathering profiles of contrasting climate

The abundance and oxidations states (II, III and IV) of manganese (Mn) in a weathering profile encompassing both the soil layers (A and B horizons) and the underlaid saprolite (C horizons) determine the availability of Mn as a plant nutrient and regulate its role in cycles of other elements in Earth’s critical zone. However, it remains unclear how the abundance and oxidation states vary with depth under different climates, and how the soil forming processes and soil properties control the variations. We examined four forest granite weathering profiles developed under climates ranging from temperate to tropical climate. Regardless of climate types, all four profiles showed similar vertical variation patterns of Mn concentration and oxidation states. The major features of the patterns can be understood from the perspective of soil forming processes and soil properties. Climate affected the Mn oxidation states in the fine fraction (< 2 mm) of the poorly weathered saprolite by controlling the weathering degree of Mn-bearing primary minerals. The weathering released Mn(II) and Mn(III) in the primary minerals to the circumneutral environment where it was subsequently oxidized by O2. In contrast, climate affected the Mn oxidation states in the soil layers poor in parent materials largely by controlling soil redox conditions and pH because most of the Mn in soils were reactive. As the climate became warmer/wetter, the weathering intensified and soils became more reducing and acidic, resulting in more reduced Mn in soil and more oxidized Mn in the fine fraction of saprolite. Moreover, relative to Mn(II) and Mn(IV), Mn(III) preferentially accumulated in the subsoil (B horizons), likely as Mn(III) oxyhydroxides in the colder and drier climates, and as a substitute ion in well-crystallized Fe(III) oxides in the warmer and wetter climates. These findings improve our understanding of Mn availability and cycling and its role in biogeochemical cycles of other elements in Earth’s critical zone.

Cr3+doped α-Fe2O3 nanoparticles for photodegradation of organic pollutants with their disinfection efficacy

Pristine and Cr-doped α-Fe2O3 nanoparticles were synthesized using a low-cost and simple one-step hydrothermal method without any precipitating agent. Cr-doped α-Fe2O3 was found to be a promising candidate for recyclable photocatalytic application for Tetracycline (TC) and Congo-red (CR) degradation under normal sunlight irradiation along with excellent antibacterial properties. Addition of Cr shows a significantly improved degradation efficiency from 20% to 91% in just 25 min for CR, while the degradation rate reached to 81% for TC, which was also monitored in real-time using internet of things (IoT). Also, a high degree of mineralization was achieved (∼87.9%), which was confirmed using total organic carbon (TOC) content. In parallel, the biochemical oxygen demand/chemical oxygen demand (BOD5/COD) ratio confirmed the fast degradation efficiency using a small amount of catalytic dosage (∼ 0.40 g/L). Also, degradation of multiple dyes provides a promising avenue for addressing complex waste water treatment challenges. Moreover, Cr-doped α-Fe2O3 displays excellent antibacterial activity towards E.coli and E.Faecium. Major factors involved in sunlight driven photocatalytic activity for example absorbance range, porosity, separation between e--h+, and charge transfer property were surprisingly improved by Cr doping and henceforth increased photocatalytic activity and antibacterial properties. This work highlights the potential utilization of Cr-doped α-Fe2O3 for the purification and disinfection of industrial waste water.

Ensuring the normalization of the aero-ionic regime in production areas by means of ultrasonic air ionization

The results of studies on the normalization of the aeroionic regime in rooms under ultrasonic ionization of humidified air are presented. The increase in the concentration of negative aeroions under these conditions by the combined effect of the balloelectric effect and ultrasonic cavitation is substantiated. It has been established that when distilled water is used as a source of air ions under the action of a 10 W ultrasonic generator at a distance of 0.5 m, the concentration of negative air ions increases almost sixfold. At the same time, due to the joint effect of ultrasonic cavitation in the surface layer of water and the balloelectric effect, no generation of ozone and nitrogen oxides is caused. It is proved that with a decrease in the degree of water mineralization, the concentrations of negative and positive aeroions increase due to changes in the physicochemical properties of water and the resulting mechanochemical phenomena. The mechanism of formation of air ions in the air of industrial premises under the combined action of the balloelectric effect and ultrasound is proposed. It is substantiated that the quality of the air ionic composition of industrial premises air improves at a temperature of demineralized water of 20-25 °C and a directed air flow of 6 m/s towards the working area with the combined effect of ultrasound and balloelectric effect, which contributes to the improvement of sanitary and hygienic working conditions. The structure of an automated system for controlling the aeroionic regime of the working area of industrial premises with artificial ionization of humidified air using an aeroion generator and a ventilation system is proposed. This will allow monitoring and processing of information on technological, electrical and microclimatic parameters, adjusting, coordinating and jointly controlling the ventilation system devices and the ultrasonic generator of air ions.

Enhanced Photocatalytic Paracetamol Degradation by NiCu-Modified TiO2 Nanotubes: Mechanistic Insights and Performance Evaluation.

Anodic TiO2 nanotube arrays decorated with Ni, Cu, and NiCu alloy thin films were investigated for the first time for the photocatalytic degradation of paracetamol in water solution under UV irradiation. Metallic co-catalysts were deposited on TiO2 nanotubes using magnetron sputtering. The influence of the metal layer composition and thickness on the photocatalytic activity was systematically studied. Photocatalytic experiments showed that only Cu-rich co-catalysts provide enhanced paracetamol degradation rates, whereas Ni-modified photocatalysts exhibit no improvement compared with unmodified TiO2. The best-performing material was obtained by sputtering a 20 nm thick film of 1:1 atomic ratio NiCu alloy: this material exhibits a reaction rate more than doubled compared with pristine TiO2, enabling the complete degradation of 10 mg L-1 of paracetamol in 8 h. The superior performance of NiCu-modified systems over pure Cu-based ones is ascribed to a Ni and Cu synergistic effect. Kinetic tests using selective holes and radical scavengers unveiled, unlike prior findings in the literature, that paracetamol undergoes direct oxidation at the photocatalyst surface via valence band holes. Finally, Chemical Oxygen Demand (COD) tests and High-Resolution Mass Spectrometry (HR-MS) analysis were conducted to assess the degree of mineralization and identify intermediates. In contrast with the existing literature, we demonstrated that the mechanistic pathway involves direct oxidation by valence band holes.

Source and Origin of Subsurface Brine of the Kongquehe Sag Area in Western Lop Nur, China

The Kongquehe Sag, located in the western Lop Nur, has abundant pore subsurface brine. In order to study the source and origin, we tested and analyzed the hydrochemical composition and stable isotopes of the subsurface brine. The findings reveal that the brine exhibits a moderate to low degree of mineralization, with values ranging from 50.50 g/L to 91.14 g/L. The stable isotope compositions of unconfined and confined waters are different, with the mean values of δD being −8.00‰ and −51.75‰ and the mean values of δ18O being 10.08‰ and −6.01‰. These values are indicative of an intense evaporative environment prevalent in the Kongquehe Sag area. Furthermore, the 87Sr/86Sr ratios vary between 0.710642 and 0.710837, and δ34S values range from 9.2 to 10.7. These data suggest the long-term evolution of sulfur substances, predominantly through dissolution and sedimentation processes, with minimal influence from redox reactions. The data garnered from this research not only offer a novel perspective of the insights gained into the hydrochemical characteristics and the stable isotope signatures of the brines in the Kongquehe Sag area but also enriches the theoretical framework concerning the source and origin of subsurface brines, potentially informing future exploration strategies.

Combined effect of magmatic fluid–seawater mixing and host rock alteration on the formation of gold-enriched massive sulfides in the Forecast vent field, southern Mariana Trough

Massive sulfides and sulfide-bearing breccia were collected from the Forecast vent field in the southern Mariana Trough. These samples exhibit varying degrees of hydrothermal alteration and/or mineralization, with the former type having significant enrichments in Au (up to 101 ppm). In this study, detailed analyses of mineralogy, geochemistry, S isotope, and fluid inclusion were conducted to understand the unusual Au-rich mineralization. Mineralogical investigations and geochemical analyses (LA–ICP–MS and EPMA) of dominant sulfide minerals indicate that electrums, the main phase of Au mineralization, are characterized by two different generations based on mineralogical relationships and fineness. Early-stage high fineness electrums (930–981 ‰) are associated with sphalerite under relatively high-temperature fluid conditions, whereas galena is main host mineral related to late-stage low fineness electrums (773–868 ‰). Sphalerite geothermometry (231–264 °C), the occurrence of colloform textured sulfides, and microthermometric characteristics of fluid inclusions (Th = 220–304 °C; Salinity = 1.4–6.6 wt% NaCl equivalent; a general trend of decreasing salinity with decreasing Th) indicate that significant decreases in H2S activity, attributed to seawater dilution and rapid precipitation of sulfide minerals, facilitated the efficient destabilization and deposition of Au transported as sulfide complexes from hydrothermal fluids. In particular, the lower 34S values (+0.2 ‰ to + 1.3 ‰) of sulfides compared to those of arc/back-arc lavas (δ34S = +5‰ to + 11 ‰), along with the prevalence of CO2 in the vapor phase of fluid inclusions, reflect that the significant contribution of magmatic volatile influx supplied most of the sulfur and metals (including Au) to the Forecast hydrothermal fluids. Additionally, the abundance of montmorillonite and varying proportions of sulfide and gangue minerals observed in hydrothermal samples suggest that the chemical buffering of fluids by associated substrates and/or sediments could be another significant factor in promoting Au-rich mineralization. Therefore we conclude that the combination of magmatic fluid–seawater mixing and host rock alteration plays an important role in the formation of Au-enriched massive sulfides in the Forecast vent field.

LaCuMnOx perovskite activating persulfate for the degradation of bisphenol A: excellent tolerance to hypersaline environment

AbstractBackgroundLaCuMnOx (LCMO) perovskite was designed as an effective catalyst to activate peroxydisulfate (PDS) to remove bisphenol A (BPA) in hypersaline wastewater.ResultsIn the LCMO/PDS system, BPA (10 mg/L) was removed completely and the mineralization degree reached 74.9% in the presence of 0.12 g/L catalyst and 1.2 mM PDS. The BPA removal efficiency was still almost 100% even after five cycles. Metal ion leakage also indicated the stability of the catalytic system. •OH, SO4•−, 1O2, and O2•− all contributed to BPA removal, and O2•− accounted for the greatest contribution. The presence of oxygen vacancies (Vo··) on the surface of the catalyst was important for PDS activation and the formation of active species. In addition, the system could still maintain outstanding performance even when [Cl−] and [SO42−] were 100 g/L. CO32− and HCO3− inhibited BPA degradation greatly, even at very low concentrations. The inhibitory effect was related to changes in the pH of the solution caused by the addition of CO32− and HCO3−. This effect could be eliminated by adjusting the pH.ConclusionThe system showed excellent catalytic performance, stability, and inorganic anion tolerance, indicating its potential for application in hypersaline wastewater treatment. © 2024 Society of Chemical Industry (SCI).

Enhanced mineralization of pharmaceutical residues at circumneutral pH by heterogeneous electro-Fenton-like process with Cu/C catalyst

Conventional electro-Fenton (EF) process at acidic pH ∼3 is recognized as a highly effective strategy to degrade organic pollutants; however, homogeneous metal catalysts cannot be employed in more alkaline media. To overcome this limitation, pyrolytic derivatives from metal-organic frameworks (MOFs) have emerged as promising heterogeneous catalysts. Cu-based MOFs were prepared using trimesic acid as the organic ligand and different pyrolysis conditions, yielding a set of nano-Cu/C catalysts that were analyzed by conventional methods. Among them, XPS revealed the surface of the Cu/C-A2-Ar/H2 catalyst was slightly oxidized to Cu(I) and, combined with XRD and HRTEM data, it can be concluded that the catalyst presents a core-shell structure where metallic copper is embedded in a carbon layer. The antihistamine diphenhydramine (DPH), spiked into either synthetic Na2SO4 solutions or actual urban wastewater, was treated in an undivided electrolytic cell equipped with a DSA-Cl2 anode and a commercial air-diffusion cathode able to electrogenerate H2O2. Using Cu/C as suspended catalyst, DPH was completely degraded in both media at pH 6–8, outperforming the EF process with Fe2+ catalyst at pH 3 in terms of degradation rate and mineralization degree thanks to the absence of refractory Fe(III)-carboxylate complexes that typically decelerate the TOC abatement. From the by-products detected by GC/MS, a reaction sequence for DPH mineralization is proposed.

Performance evaluation and physical simulation experiment of SiO2 nanoparticle synergistic crosslinked polymer system

Abstract As natural gas development gradually shifts from early to mid to late stages, water outflow from gas wells has become an inevitable problem. In this study, polyethyleneimine cross-linked polymers were synthesized and nano particles were introduced to obtain SiO2 nanoparticle synergistic cross-linked polymer systems. Rheological experiments show that the system has stronger shear resistance and higher yield stress, and the linear viscoelastic region has a stress amplitude less than 3.5Pa, exhibiting good elastic properties in the range of 0.01 to 10Hz. In terms of stability, after 45 days of aging, the viscosity retention rate of the system is 77.66%. When the mineralization degree is 224852mg/L, the viscosity retention rate is greater than 76.33%, indicating that the system has good aging stability and salt resistance.The physical simulation experiment of core displacement shows that SiO2 nanoparticle synergistic cross-linked polymer gel has gas-water selective plugging ability, and the reduction of water phase permeability is much greater than that of gas phase. The gas phase permeability can remains at about 75%, which is 2300 times that of water phase permeability, and has a good water plugging effect.