Inorganic Ions Research Articles

Identification of Glyoxalase A in Group B Streptococcus and its contribution to methylglyoxal tolerance and virulence.

Group B Streptococcus (GBS) is a Gram-positive pathobiont that commonly colonizes the gastrointestinal and lower female genital tracts but can cause sepsis and pneumonia in newborns and is a leading cause of neonatal meningitis. Despite the resulting disease severity, the pathogenesis of GBS is not completely understood, especially during the early phases of infection. To investigate GBS factors necessary for blood stream survival, we performed a transposon (Tn) mutant screen in our bacteremia infection model using a GBS mariner transposon mutant library previously developed by our group. We identified significantly underrepresented mutations in 628 genes that contribute to survival in the blood, including those encoding known virulence factors such as capsule, the β-hemolysin, and inorganic metal ion transport systems. Most of the underrepresented genes have not been previously characterized or studied in GBS, including gloA and gloB, which are homologs for genes involved in methylglyoxal (MG) detoxification. MG is a byproduct of glycolysis and a highly reactive toxic aldehyde that is elevated in immune cells during infection. Here, we observed MG sensitivity across multiple GBS isolates and confirm that gloA contributes to MG tolerance and invasive GBS infection. We show specifically that gloA contributes to GBS survival in the presence of neutrophils and depleting neutrophils in mice abrogates the decreased survival and infection of the gloA mutant. The requirement of the glyoxalase pathway during GBS infection suggests that MG detoxification is important for bacterial survival during host-pathogen interactions.

On the selective transport of mixtures of organic and inorganic anions through anion-exchange membranes: A case study about the separation of nitrates and citric acid by electrodialysis

Electrodialysis is finding an increasing number of applications, recently also in the separation and purification of organic acids. This technology involves reducing the use of chemicals and the generation of wastes, as compared to conventionally used processes. Gaining insights about the competitive transport between organic and inorganic ions in ED systems is key to achieving efficient separation processes in the bioresource industry. In the present study, the competitive transport of organic (citrates) and inorganic anions (nitrates) through anion-exchange membranes is investigated, under varying pH conditions, ion concentrations, and applied currents, by means of chronopotentiometry and ED experiments. In the absence of nitrate ions and under acidic conditions (pH 2), the resistance of the membrane system is very high because citric acid is mainly present in its undissociated and uncharged form. In the case of sodium citrate (pH 8), the membrane resistance decreases, especially at high current densities, which promote dissociation reactions and the subsequent concentration increase in ionic species near the membrane. Such phenomenon is identified both in chronopotentiometric curves and in long-term ED experiments by a gradual drop in membrane voltage with time. Although being less concentrated than citrates, the selective removal of nitrates is the most effective choice for the separation of both types of species. The selectivity factor of nitrates over citrates reaches the highest values at low applied current densities (below the limiting current density), with stable permselectivity values higher than 20. Such conditions also lead to the least specific energy consumption per nitrates removed (<0.5 kW·hr·kgNO3--1). Therefore, ED can be used under such favorable operating conditions after a clarification step in order to remove inorganic ions from fermentation broths and increase the purity of organic acids. At higher current densities, the enhanced transport of citrate anions produces a significant drop in selectivity towards nitrates and increases the specific energy consumption.

Effects of inorganic salt ions on the wettability of deep coal seams: Insights from experiments and molecular simulations

Coal wettability plays a significant role in the efficiency of coalbed methane (CBM) extraction since it determines fluid transport and distribution. Deep coal seam aqueous fluids have a high salinity. Consequently, coal wettability experiments utilizing fresh water are not representative for those coal seams. Therefore, the effect of aqueous fluids with inorganic salt ions on coal wettability needs to be investigated. In this study, both experiments and molecular simulations are conducted to unravel the wetting behaviour and mechanisms of saline fluids on coal surfaces, investigating different fluid salt concentrations, temperatures, valence states, and coal pore sizes. The results reveal that a more saline fluid displays a more hydrophobic behaviour on the coal surface. Microscopically, water molecules have a tendency to assemble around cations and anions as hydration shells and gradually detach from the coal surface, leading to a gradual transition from hydrophilicity to hydrophobicity. A change in wettability with fluid salinity can be caused by two mechanisms. On the one hand, an increase in ion concentration constrains the diffusion of water molecules through hydration, weakening the mobility of water molecules. On the other hand, a higher ion concentration weakens the interaction between water molecules and oxygen-containing functional groups, reducing the affinity of the water molecules with the pore wall. Moreover, at higher temperatures, ion valence states, and for coal with smaller pores, the impact of inorganic salt ions in fluids on the wetting behaviour of coal surfaces becomes more significant. The coal wettability influences the capillary pressure of coal pores. This study provides new insights on the effect of saline fluids on coal wettability which may help address challenges of fracturing fluid loss and water-blocking in CBM production activities.

From Waste to Water Purification: Textile-Derived Sorbents for Pharmaceutical Removal.

The presence of pharmaceuticals or their active metabolites in receiving waters is a sign of the inefficient removal of bioactive substrates from wastewater. Adsorption seems to be the most effective and inexpensive method of their removal. Waste management aimed at sorbents is a promising way to sustain several sustainable development goals. In the presented paper, the removal of the two most widely used drugs in the wastewater was examined. Diclofenac and carbamazepine were removed from water and wastewater using textile waste-derived sorbents. Their removal efficiency was verified by testing several process parameters such as the time of the sorption, the presence of interfering inorganic ions, the presence of dissolved organic matter, the initial pH and ionic strength of the solution, and various water matrices. The adsorption capacity was noted for diclofenac (57.1 mg/g) and carbamazepine (21.25 mg/g). The tested process parameters (pH, presence of inorganic ions, dissolved organic matter, ionic strength, water matrix) confirmed that the presented waste materials possessed a great potential for pharmaceutical removal from water matrices.

Determination of nutrient concentration in liquid culture of cyanobacteria Nostoc sp. by capillary electrophoresis and inductively coupled plasma mass spectrometry

In this work, we demonstrate the use of capillary electrophoresis and inductively coupled plasma mass spectrometry, as competitive methods primarily for ion chromatography, to determine changes in the concentration of small inorganic ions in the Nostoc sp. culture medium. Although macronutrients were analyzed by capillary electrophoresis with conductivity detection, micronutrients were analyzed by inductively coupled plasma mass spectrometry. The different light settings (light intensity and spectral composition) had a visible effect on the culture growth and depletion of calcium, magnesium, and phosphate ions, and iron and manganese elements when comparing the behavior under red or violet light with that under blue light.

Evaluating The Impact of Increased Heavy Oil Consumption on Urban Pollution Levels through Isotope (δ13C, δ34S, 14C) Composition

The impact of heavy fuel oil (HFO) on the chemical and isotopic composition of submicron particulate matter (PM1) was investigated. For this purpose, we conducted an analysis of water-soluble inorganic ions (WSIIs) and multiple isotopes (δ34S, δ13C, 14C) of PM1 and SO2 collected during two heating periods: before (2021–2022) and during the use of HFO (2022–2023) in Vilnius, Lithuania. The results showed that the combustion of HFO increased the concentrations of SO₂ (by 94%) and PM1-related sulfate (by 30%). It also altered the chemical composition of PM1, with sulfate becoming the predominant component (~40%) of WSIIs. The stable sulfur isotope ratios of SO2 (δ34SSO2) and sulfate (δ34SPM1) shifted significantly to more negative values (δ34SSO2 = 0.4‰, δ34SPM1 = −0.3‰) compared to the previous heating period. Anticorrelation between δ¹³C and δ³⁴S values indicated increased contributions of ¹³C-enriched fossil fuel sources (coal and HFO) in EC, although the share of fossil fuels in elemental carbon (EC) slightly decreased during the HFO period. The combustion of HFO affected the concentrations of PM1 chemical components and substantially impacted the isotopic composition and source contributions of sulfate and EC.

Comparative evaluation of sensory and instrumental flavor profiles of four edible microalgae: Spirulina platensis, Chlorella pyrenoidosa, Chlamydomonas reinhardtii, and Haematococcus pluvialis

Microalgae sensory features are an important parameter to consider in food applications. The current study comparatively evaluated the flavor profiles of four commercial edible microalgae species, i.e., Spirulina platensis, Chlorella proteinosa, Chlamydomonas reinhardtii, and Haematococcus pluvialis through sensory evaluation by a trained expert panel (n = 15) and chemical profiling of flavor compounds, with multivariate statistical methods used to correlate descriptive taste and odor analysis with non-volatile and volatile compounds. S. platensis displayed characteristic salty and umami tastes arising from inorganic ions and 5′-nucleotides, respectively, as well as “muddy” and “floral” odor attributes mainly associated with sulfur compounds and ketones. C. proteinosa and C. reinhardtii shared the taste attributes of sweetness and bitterness mainly contributed by free amino acids, as well as the odor attributes of “seaweed” and “mushroom” in association with aldehydes and alcohols. H. pluvialis had a typical sour taste owning to the presence of abundant organic acids, and smelled “fatty”, “phenolic”, “licorice”, and “fruity” due to aromatic ester and phenolic compounds. Overall, our results provide fundamental insights into the sensory features of common edible microalgae to guide future food applications.

Automated Identification of Ions Observed in Mass Spectra of Inorganic Compounds Using Isotopic Distribution Brute Force: Methodology and Performance Measurements.

This Article describes the method of isotopic distribution brute force, which can be used to identify ions registered in mass spectra of inorganic compounds in an automated manner when a library search cannot be conducted. A detailed description of the isotopic distribution brute force methodology is presented, including a discussion of computation-related difficulties. The ability of the proposed algorithm to identify various inorganic ions is tested on a small set of real-life low-resolution mass spectra of lead halides and copper halides. An evaluation of the isotopic distribution brute force performance is conducted using the low-resolution experimental mass spectra of natural rhenium sulfide and lead(II) chloride. Based on identification results and obtained performance measurements, we formulate the empirical restrictions on the input data, ensuring that the application of isotopic distribution brute force is feasible from the standpoints of search space reduction and identification time.

Estimation of Particulate Matter (PM10) Over Middle Indo-Gangetic Plain (Patna) of India: Seasonal Variation and Source Apportionment

Despite extensive research on particulate matter (PM) pollution in India’s Indo-Gangetic Plain (IGP), source apportionment remains challenging. This study investigates the effect of particulate matter (PM10)-associated water soluble inorganic ions (WSIIs) on ambient air concentration across the middle IGP from January to December 2018. Moreover, the seasonal fluctuation and chemical characterization of PM10 were assessed for the year 2018. The results revealed a high concentration of PM10 (156 µg/m3), exceeding the WHO and National Ambient Air Quality Standard (NAAQS) limits. The highest PM10 levels were observed during autumn, winter, summer, and the rainy season. The study identified SO42− and NH4+ as the most common WSIIs, constituting 46% and 23% of the total WSIIs. Source apportionment analysis indicated that street dust, biomass burning, and vehicle and industrial emissions together with secondary formation significantly contributed to IGP’s PM pollution. Additionally, the investigation of air mass back trajectory suggests that air quality in IGP is largely influenced by eastern and western Maritime air masses originated from the Arabian Sea, the Bay of Bengal, Gujarat, Afghanistan, Pakistan, and Bangladesh.

Modulating Cu2O/CuO on attapulgite for boosting peroxymonosulfate activation

Peroxymonosulfate (PMS) activation is an economically viable and efficient advanced oxidation process used to degrade recalcitrant organic pollutants. In this study, the copper oxide/attapulgite (CuxO/ATP) catalyst was synthesized via the hydrothermal method. The catalytic degradation efficiency was assessed using ciprofloxacin (CIP) as the model pollutant. The influence of catalyst dosage and PMS concentration on CIP degradation was examined. Additionally, the capability of the catalyst to degrade CIP under varying pH conditions, temperatures, and in the presence of diverse inorganic ions was investigated. The findings revealed that CuxO/ATP exhibited superior performance compared to pure CuxO in PMS activation for CIP degradation. Microstructural analysis indicated well-dispersed CuxO nanoflowers on the attapulgite, facilitating a synergistic effect between the two components. The presence of attapulgite enhanced the dispersion of CuxO, leading to an increase in the exposed surface area. In addition, attapulgite facilitated the adsorption of pollutants onto the CuxO interface, while CuxO, in turn, activated PMS to generate active free radicals, thereby enabling the catalytic oxidation of pollutants. Through a series of free radical quenching experiments, sulfate radicals were identified as the predominant species responsible for CIP degradation, playing a pivotal role in the system. Moreover, a plausible catalytic mechanism was discussed. Furthermore, reusability tests demonstrated the catalyst's stability and recyclability. This research not only presents a novel and robust approach for CuxO catalyst synthesis but also offers deeper insights into the mechanism underlying CuxO activation of PMS.

A Series of Lanthanide Coordination Polymers as Luminescent Sensors for Selective Detection of Inorganic Ions and Nitrobenzene.

Seven new lanthanide coordination polymers, namely [Ln(cpt)3H2O)]n(Ln = La (1), Pr (2), Sm (3), Eu (4), Gd (5), Dy (6), and Er (7)), which were synthesized under hydrothermal conditions using 4'-(4-(4-carboxyphenyloxy)phenyl)-4,2':6',4'-tripyridine (Hcpt) as the ligand. The crystal structures of these seven complexes were determined using single-crystal X-ray diffraction, and they were found to be isostructural, crystallizing in the triclinic P1- space group. The Ln(III) ions were nine-coordinated with tricapped trigonal prism coordination geometry. The Ln(III) cations were coordinated by carboxylic and pyridine groups from (cpt)- ligands, forming one-dimensional ring-chain structures. Furthermore, the luminescent properties of complexes 1-7 were investigated using fluorescent spectra in the solid state. The fluorescence sensing experiments demonstrated that complex 4 exhibits high selectivity and sensitivity for detecting Co2+, Cu2+ ions, and nitrobenzene. Moreover, complex 3 shows good capability for detecting Cu2+ ions and nitrobenzene. Additionally, the sensing mechanism was also thoroughly examined through theoretical calculations.

Autocatalytic degradation of Cu-EDTA in the Calcite/PMS system: Singlet oxygen and Cu(III)

The simultaneous removal of heavy metal complexes (HMCs) and heavy metal ions presents a significant challenge in treating wastewater. To address this, we propose a Calcite/Peroxymonosulfate (Calcite/PMS) system aimed at simultaneously decomplexing Cu-EDTA and removing Cu ions. Calcite/PMS system could achieve 99.5 % Cu-EDTA decomplexation and 61.9 % Cu ions removal within 60 min under initial conditions of Cu-EDTA (10 mg/L), Calcite (3 g/L), and PMS (2 mM). Singlet oxygen (1O2) emerged as the predominant reactive species responsible for Cu-EDTA decomplexation, which selectively targeted the N-C bonds in the Cu-EDTA structure to produce intermediates with lower biotoxicity than EDTA. Interestingly, solid phase Cu(III) (≡Cu(III)) promoted the generation of superoxide radicals (O2•−) with a contribution of up to 72.8 %. Subsequently, nascent ≡Cu(III) and O2•− accelerated the degradation of intermediates. Besides, coexisting organic substances inhibited Cu-EDTA decomplexation, whereas inorganic ions had a weak impact. After five cycles of use, the Calcite/PMS system retained 99.3 % efficiency in decomplexing Cu-EDTA. This investigation provides valuable insights into using calcite to remove HMCs and enhances our comprehension of the decomplexation intermediates accelerating HMCs degradation.

Long-term change in winter aerosol composition and sources in Guiyang Southwest China (2003–2020)

This study presents a comprehensive analysis of air quality in China, Southwest China, over four winter seasons: 2003–2004, 2004–2005, 2017–2018 and 2019–2020. We initially collected Total Suspended Particles (TSP) samples during the earlier periods and PM2.5 samples during the later periods. Our goal was to illustrate the changes in sources of atmospheric pollutants over time. By focusing on the chemical composition of water-soluble inorganic ions (WSIIs), we highlighted significant long-term changes in air quality and pollution sources in Guiyang alongside the effectiveness of recent pollution treatment strategies. Historically affected by acid rain and acid pollution, Guiyang has shown notable improvements in air quality. Notably, sulfate pollution, primarily from coal combustion, has significantly decreased, with the sulfates concentration declining from an estimated 19.04 μg m−3 to 30.46 μg m−3 during the winter of 2003–2004, to just 7.37 μg m−3 in PM2.5 during the winter of 2019–2020. Additionally, the mean mass concentration of PM2.5 dropped by 18% between the 2017–2018 and 2019–2020 winters. An increasing ratio of nitrate to sulfate in the aerosols indicates a shift in pollution sources, with secondary nitrate pollution, largely from vehicle emissions, becoming increasingly prevalent. Positive Matrix Factorization (PMF) model analysis identified five major pollution sources, highlighting a transition from secondary sulfate to secondary nitrate as the primary contributors to air pollution in Guiyang, and secondary nitrate pollution mainly from vehicles emission was increasingly severe meanwhile the significance of ammonium should not be overlooked. The results stress the importance of local pollution sources and suggest a need for revised pollution control policies that address the evolving characteristics of aerosols and prioritize the major pollutants in Guiyang, especially during winter months.

Synergy of pore confinement and co-catalytic effects in Peroxymonosulfate activation for persistent and selective removal of contaminants

The activation of peroxymonosulfate (PMS) through nanoconfinement and co-catalytic effects has demonstrated considerable promise in environmental remediation. Nevertheless, the attainment of persistent efficiency and specificity for pollutant degradation remains a formidable obstacle. Herein, we proposed a solvent-free molten approach to convert a mixture of zeolitic imidazolate frameworks (ZIFs) and MoS2 into 3D integrated cobalt-molybdenum bimetallic nitrogen-doped porous carbon foam with catalytic/co-catalytic performance (MC@NCF). The integrated materials exhibited exceptional efficiency in degrading contaminants based on the synergy of pore confinement and co-catalytic effects, achieving almost 100 % tetracycline degradation in 10 min with a k-value as high as 112.44 min−1·M−1, which was superior to the existing catalysts reported so far. The experimental findings revealed that the structural adjustment of MC@NCF significant accelerated the mass transfer through the formation of interfacial Mo-S/O-Co and Mo-N-Co/C bonds electron-tuning bridges between pore-confined micro-units, leading to the increased singlet oxygen (1O2) yield. Therefore, the MC@NCF exhibited more remarkable stability without interference from coexisting inorganic ions and cations, humic acid, and water matrices. Moreover, a flow-through nanoreactor was constructed and acquired efficient reactivity with negligible biotoxicity, and easy nanocatalyst recycling after continuous operation. The possible reactivity mechanism was identified by Frontier molecular orbital theory HOMO-LUMO, Fukui function, LC-MS, EPR, in-situ ATR-FTIR, and Raman analyses. Our results will guide integrated “catalytic/co-catalytic” nanoconfined MOF derivatives design to further enhance deep water purification technology.

Tetracycline degradation in the system of peracetic acid activation by liquid discharge plasma

The oxidative degradation ability of peracetic acid (PAA) for organic pollutants can be enhanced by different activation methods. This study investigated the degradation efficiency and mechanisms of tetracycline (TC) using PAA activated by liquid-phase discharge plasma. An 86.08 % degradation efficiency for TC after 60 min treatment was achieved in the Plasma/PAA system, much higher than that of the sole Plasma (46.64 %) and PAA (15.19 %). Acidic conditions and neutral conditions were more favorable for TC removal than alkaline conditions. Inorganic ions generally inhibited TC degradation, though notably, low concentrations of Cl− and NO3− promoted it. Free radical quenching experiments and electron paramagnetic resonance (EPR) analysis confirmed the crucial roles of OH, RO, and 1O2 in TC degradation. Three-dimensional fluorescence spectroscopy (3DFS) and ultraviolet–visible absorption spectroscopy (UV–VIS) elucidated the TC degradation mechanism, revealing key aspects of antibiotic structural decomposition. Further analysis of the degradation products by liquid chromatography-mass spectrometry (LC-MS) indicated three potential degradation pathways. Biotoxicity evaluations indicated that the synergistic system significantly reduced the biotoxicity of the degradation products. This study demonstrated an efficient method for plasma-activated PAA in degrading persistent pharmaceutical pollutants. It also confirmed the system’s applicability across a broad spectrum of organic pollutants and water bodies, highlighting its potential for a wide range of environmental protection applications.

Hygroscopic Properties of Water-Soluble Counterpart of Ultrafine Particles from Agriculture Crop-Residue Burning in Patiala, Northwestern India

To determine the link between hygroscopicity and the constituent chemical composition of real biomass-burning atmospheric particles, we collected and analyzed aerosols during wheat-straw (April–May), rice-straw (October–November), and no-burning periods (August–September) in 2008 and 2009 in Patiala, Punjab. A hygroscopicity tandem differential mobility analyzer (HTDMA) system was used to measure hygroscopicity at ~5 to ~95% relative humidity (RH) of aerosolized 100 nm particles generated from the water extracts of PM0.4 burning and no-burning aerosol samples. The chemical analyses of the extracts show that organic carbon and water-soluble inorganic-ion concentrations are 2 to 3 times higher in crop-residue burning aerosol samples compared to no-burning aerosols, suggesting the substantial contribution of biomass burning to the carbonaceous aerosols at the sampling site. We observed that aerosolized 100 nm particles collected during the crop-residue burning period show higher and more variable hygroscopic growth factor (g(RH)) ranging from 1.21 to 1.68 at 85% RH, compared to no-burning samples (1.27 to 1.33). Interestingly, crop-residue burning particles also show considerable shrinkage in their size (i.e., g(RH) &lt; 1) at lower RH (&lt;50%) in the dehumidification mode. The increased level of major inorganic ions in biomass-burning period aerosols is a possible reason for higher g(RH) as well as the observed particle shrinkage. Overall, the measured g(RH), together with the correlation observed between aerosol water content and ionic-species volume fraction, and the study of the abundance of individual constituent ionic species suggests that inorganic salts and their proportion in aerosol particles primarily governed the aerosol hygroscopicity.

Metabolomic Disparities in Intraocular Fluid Across Varied Stages of Cataract Progression: Implications for the Analysis of Cataract Development.

Introduction: The lens's metabolic demands are met through a continuous circulation of aqueous humor, encompassing a spectrum of components such as organic and inorganic ions, carbohydrates, glutathione, urea, amino acids, proteins, oxygen, carbon dioxide, and water. Metabolomics is a pivotal tool, offering an initial insight into the complexities of integrated metabolism. In this investigative study, we systematically scrutinize the composition of intraocular fluid in individuals afflicted with cataracts. Methods: The investigation involved a comprehensive analysis of aqueous humor samples from a cohort comprising 192 patients. These individuals were stratified by utilizing the SPONCS classification system, delineating distinct groups characterized by the hardness of cataracts. The analytical approach employed targeted quantitative metabolite analysis using HILIC-based liquid chromatography coupled with high-resolution mass spectrometric detection. The metabolomics data analysis was performed with MetaboAnalyst 5.0. Results: The results of the enrichment analysis have facilitated the inference that the discerned disparities among groups arise from disruptions in taurine and hypotaurine metabolism, variations in tryptophan metabolism, and modifications in mitochondrial beta-oxidation of short-chain saturated fatty acids and pyrimidine metabolism. Conclusion: A decline in taurine concentration precipitates diminished glutathione activity, prompting an elevated requirement for NAD+ and instigating tryptophan metabolism along the kynurenine pathway. Activation of this pathway is additionally prompted by interferon-gamma and UV radiation, leading to the induction of IDO. Concurrently, heightened mitochondrial beta-oxidation signifies a distinctive scenario in translocating fatty acids into the mitochondria, enhancing energy production.

Visible light-enhanced interface interaction for PMS activation towards the removal of emerging organic pollutants: performance, mechanism and toxicity

The peroxymonosulfate (PMS)-based advanced oxidation process is considered as an effective way to remove emerging organic pollutants in the wastewater. However, the heterogeneous catalysts used for PMS activation suffers from low catalytic stability and PMS utilization efficiency. Herein, sulfur-doped cobalt ferrite loaded graphitic carbon nitride (S-CoFe2O4/CN) was firstly synthesized for PMS activation toward the sulfamethoxazole (SMX) removal. The S-CoFe2O4/CN possessed excellent PMS catalytic activity and photocatalytic activity. The first-order kinetic constant (k) of SMX degradation in the presence of visible light reached 0.3564 min−1 with high PMS utilization efficiency (78.3 %). Mechanism analysis elucidated that compared to the original CoFe2O4, sulfur doping created more oxygen vacancies, while visible light further promoted the regeneration of Co(II), Fe(II) and oxygen vacancy, the formation of high-valent iron oxo as well as the reduction of S2- oxidation. In addition, the visible light/S-CoFe2O4/CN/PMS system showed high resistance to inorganic ions, and superior catalytic stability. Both acute and chronic toxicity of treated SMX solution decreased. This study provides an effective system to remove emerging organic pollutants in the wastewater.

Controlling the amount of MoSe2 loaded SrTiO3 to activate peroxymonosulfate for efficient elimination of organic pollutants

ABSTRACT It is critical to effectively eliminate recalcitrant organic pollutants from wastewater. In this paper, the MoSe2/SrTiO3 (MST) catalysts were synthesized through simply controlling the amount of MoSe2 in the hydrothermal method to activate peroxymonosulfate (PMS) for the degradation of pollutants. The results demonstrated that sulfamethoxazole and tetracycline were almost eliminated by PMS/MST-3 (MoSe2/SrTiO3 mass ratio 0.3: 1) activation system. The effect of inorganic anions (Cl –, H2PO4 –, HCO3 –) and metal ions (Cu2+, Ni2+, Zn2+) commonly found in actual water bodies on catalytic reaction was explored. Moreover, SO4 • –, •OH and 1O2 were identified by EPR tests and scavenger experiments, where the SO4 • – and •OH were the dominant reactive species. The XPS analysis indicated that the oxygen vacancies and charge transfer on the catalyst surface were the keys of PMS activation. The effect of active sites in SMX and TC on the catalytic degradation activity was explored by density functional theory, and it was obtained that the central nitrogen site of SMX was more vulnerable in the catalytic system, while the edge oxygen site of TC was more susceptible to attack.

MnFe2O4/MoS2 catalyst used for ozonation: optimization and mechanism analysis of phenolic wastewater treatment.

The performance of catalytic ability of MFe2O4/MoS2 in the ozonation process was investigated in this work. The synthesized MnFe2O4/MoS2 was optimize prepared and then characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photo-electron spectroscopy, and magnetic saturation strength. The results showed that when Cphenol = 200 mg/L, initial pH = 9.0, Q = 0.10 L/min, and CMnFe2O4/MoS2 = 0.10 g/L, MnFe2O4/MoS2 addition improved the degradation efficiency of phenol by 20.0%. The effects of pH, catalyst dosage, and inorganic ions on the phenol removal by the MnFe2O4/MoS2 catalytic ozonation were investigated. Five cycle experiments proved that MnFe2O4/MoS2 had good recyclability and stability. MnFe2O4/MoS2 also showed good catalytic performance in the treatment of coal chemical wastewater pesticide wastewater. The MnFe2O4 doped with MoS2 could provide abundant surface active sites for ozone and promote the stable cycle of Mn2+/Mn3+and Fe2+/Fe3+, thus generating large amounts of •OH and improving the degradation of phenol by ozonation. The MnFe2O4/MoS2/ozonation treatment system provides a technical reference and theoretical basis for industrial wastewater treatment.