Oxidation Rate Research Articles

Iron minerals enhance Fe(II)-mediated abiotic As(III) oxidation

The abiotic oxidation of As(III) is simultaneously mediated by the oxidation of Fe(II) in microaerobic environment, but the role of Fe minerals in the Fe(II)-mediated As(III) oxidation have been neglected. This work mimicked the microaerobic environment and examined the mechanisms of Fe(II) mediated the As(III) oxidation in the presence of Fe minerals using a variety of iron minerals (lepidocrocite, goethite, etc.). The results indicated the Fe(II) and As(III) oxidation rate were improved with Fe minerals, while As(III) oxidation efficiency increased by 1.3–1.8 times in comparison to that without minerals. Fe(II) mediated the As(III) oxidation happened on Fe minerals surface in the presence of Fe minerals. The As(III) oxidation efficiency increased with increasing Fe mineral concentrations (from 0.5 to 2 g L-1) but decreased with increasing pH values. Reactive oxygen species (ROS) that play a crucial role in As(III) oxidation were Fe(IV) and ·O2-, accounting for 42.7%–47.9% and 24.1%–29.8%, respectively. The Fe minerals facilitated the oxidation of As(III) by ROS and stimulated the release of ROS through the adsorbed-Fe(II) oxidation, both of which favored As(III) oxidation. This work highlighted the potential mechanisms of Fe minerals in promoting Fe(II) mediated the As(III) oxidation in microaerobic environment, especially in terms of As(III) oxidation efficiency, shedding a valuable insight on optimization of arsenic contaminated wastewater treatment processes.

Metatranscriptomic response of deep ocean microbial populations to infusions of oil and/or synthetic chemical dispersant.

Oil spills are a frequent perturbation to the marine environment that has rapid and significant impacts on the local microbiome. Previous studies have shown that exposure to synthetic dispersant alone did not enhance heterotrophic microbial activity or oxidation rates of specific hydrocarbon components but increased the abundance of some taxa (e.g., Colwellia). In contrast, exposure to oil, but not dispersants, increased the abundance of other taxa (e.g., Marinobacter) and stimulated hydrocarbon oxidation rates. Here, we advance these findings by interpreting metatranscriptomic data from this experiment to explore how and why specific components of the microbial community responded to distinct organic carbon exposure regimes. Dispersant alone was selected for a unique community and for dominant organisms that reflected treatment- and time-dependent responses. Dispersant amendment also led to diverging functional profiles among the different treatments. Similarly, oil alone was selected for a community that was distinct from treatments amended with dispersants. The presence of oil and dispersants with added nutrients led to substantial differences in microbial responses, likely suggesting increased fitness driven by the presence of additional inorganic nutrients. The oil-only additions led to a marked increase in the expression of phages, prophages, transposable elements, and plasmids (PPTEPs), suggesting that aspects of microbial community response to oil are driven by the "mobilome," potentially through viral-associated regulation of metabolic pathways in ciliates and flagellates that would otherwise throttle the microbial community through grazing.IMPORTANCEMicrocosm experiments simulated the April 2010 Deepwater Horizon oil spill by applying oil and synthetic dispersants (Corexit EC9500A and EC9527A) to deep ocean water samples. The exposure regime revealed severe negative alterations in the treatments' heterotrophic microbial activity and hydrocarbon oxidation rates. We expanded these findings by exploring metatranscriptomic signatures of the microbial communities during the chemical amendments in the microcosm experiments. Here we report how dominant organisms were uniquely associated with treatment- and time-dependent trajectories during the exposure regimes; nutrient availability was a significant factor in driving changes in metatranscriptomic responses. Remarkable signals associated with PPTEPs showed the potential role of mobilome and viral-associated survival responses. These insights underscore the time-dependent environmental perturbations of fragile marine environments under oil and anthropogenic stress.

Oxidation behavior and corrosion resistance of CoCrFeNi high entropy alloy compared with FeCoNi medium entropy alloy

The entropy-based alloy with excellent oxidation and corrosion resistance is of great significance for practical applications in high-temperature environments. Thus, the difference in anti-oxidation property and corrosion behavior of FeCoNi MEA and CoCrFeNi HEA in a simulated marine environment was studied via a series of measurements. The results reveal that the HEA possesses superior oxidation and corrosion resistance in comparison with the MEA, which can be demonstrated by comparing the oxidation rate and thickness of oxide layer, corrosion current density (icorr) as well as corrosion morphology after polarization. The microstructure and composition of the oxide layer are the primary reasons resulting in the difference of oxidation and corrosion behaviors of the two alloys. The oxide layer with a compact, even and intact structure is produced on the HEA surface, which hinders the diffusion of detrimental ions and oxygen, whereas the loose, porous and cracked oxide layer consisting of inner Fe3O4 and outer CoO exhibits poor protection against corrosion and oxidation of the MEA. For the HEA, the preferential combination of Cr and O elements forms the protective oxide of Cr2O3, effectively enhancing corrosion resistance and inhibiting oxidation. However, the low protective CoO and relatively active Fe3O4 grow on the MEA surface, which cannot provide a good barrier to restrain oxidation and corrosion.

Oxidation Kinetics of Fluorescent Membrane Lipid Peroxidation Indicators.

The oxidation of the cellular membrane through lipid peroxidation (LPO) is linked to aging and disease. Despite the physiological importance, the chemical mechanisms underlying LPO and oxidative reactions in membranes in general remain incompletely understood, and challenges exist in translating LPO inhibitor efficacies from in vitro to in vivo. The complexity of LPO, including multiple oxidation reactions in complex membrane environments and the difficulty in quantifying reaction kinetics, underlies these difficulties. In this work, we developed a robust and straightforward method for quantifying the oxidation rate kinetics of fluorescent molecules and determined the oxidation kinetics of widely fluorophores used as indicators of membrane LPO, diphenylhexatriene (DPH), BODIPY-C11, and Liperfluo. The measurement is initiated by lipoxygenase, which provides chemical specificity and enables a straightforward interpretation of oxidation kinetics. Our results reveal that the membrane composition significantly impacts the observed kinetics oxidation in DPH and BODIPY-C11 but not Liperfluo. Reaction mechanisms for their lipid peroxide-induced oxidation are proposed. This work provides a foundation for the quantitative analysis of LPO with fluorescence and extricating the complexity of oxidation reactions within membranes.

Selective atomic sieving across metal/oxide interface for super-oxidation resistance

Surface passivation, a desirable natural consequence during initial oxidation of alloys, is the foundation for functioning of corrosion and oxidation resistant alloys ranging from industrial stainless steel to kitchen utensils. This initial oxidation has been long perceived to vary with crystal facet, however, the underlying mechanism remains elusive. Here, using in situ environmental transmission electron microscopy, we gain atomic details on crystal facet dependent initial oxidation behavior in a model Ni-5Cr alloy. We find the (001) surface shows higher initial oxidation resistance as compared to the (111) surface. We reveal the crystal facet dependent oxidation is related to an interfacial atomic sieving effect, wherein the oxide/metal interface selectively promotes diffusion of certain atomic species. Density functional theory calculations rationalize the oxygen diffusion across Ni(111)/NiO(111) interface, as contrasted with Ni(001)/NiO(111), is enhanced. We unveil that crystal facet with initial fast oxidation rate could conversely switch to a slow steady state oxidation.

Unraveling iron oxides as abiotic catalysts of organic phosphorus recycling in soil and sediment matrices

In biogeochemical phosphorus cycling, iron oxide minerals are acknowledged as strong adsorbents of inorganic and organic phosphorus. Dephosphorylation of organic phosphorus is attributed only to biological processes, but iron oxides could also catalyze this reaction. Evidence of this abiotic catalysis has relied on monitoring products in solution, thereby ignoring iron oxides as both catalysts and adsorbents. Here we apply high-resolution mass spectrometry and X-ray absorption spectroscopy to characterize dissolved and particulate phosphorus species, respectively. In soil and sediment samples reacted with ribonucleotides, we uncover the abiotic production of particulate inorganic phosphate associated specifically with iron oxides. Reactions of various organic phosphorus compounds with the different minerals identified in the environmental samples reveal up to ten-fold greater catalytic reactivities with iron oxides than with silicate and aluminosilicate minerals. Importantly, accounting for inorganic phosphate both in solution and mineral-bound, the dephosphorylarion rates of iron oxides were within reported enzymatic rates in soils. Our findings thus imply a missing abiotic axiom for organic phosphorus mineralization in phosphorus cycling.

Pleiotropic effects of an eQTL in the CELSR2/PSRC1/SORT1 cluster that associates with LDL-C and resting metabolic rate.

The locus CELSR2-PSRC1-SORT1, a primary genetic signal for lipids, has recently been implicated in different metabolic processes. Our investigation identified its association with energy metabolism. To determine biological mechanisms that govern diverse functions of this locus. Genotypes for 491,265 variants in 7,000 clinically characterized American Indians were previously determined using a custom-designed array specific for this longitudinally studied American Indian population. Among the genotyped individuals, 5,205 had measures of fasting lipid levels and 509 had measures of resting metabolic rate (RMR) and substrate oxidation rate assessed through indirect calorimetry. A genome-wide association study (GWAS) for LDL-C levels identified a variant in CELSR2 and the molecular impact of this variant on gene expression was assessed in skeletal muscle biopsies from 207 participants, followed by functional validation in mouse myoblasts using a luciferase assay. A GWAS in American Indians identified rs12740374 in CELSR2 as the top signal for LDL-C levels (P = 1 × 10-22); further analysis of this variant identified an unexpected correlation with reduced RMR (effect = -44.3 kcal/day/minor-allele) and carbohydrate oxidation rate (effect = -5.21 mg/hour/kg-EMBS). Tagged variants showed a distinct linkage disequilibrium architecture in American Indians, highlighting a potential functional variant, rs6670347 (minor-allele frequency = 0.20). Positioned in the glucocorticoid receptor's core binding motif, rs6670347 is part of a skeletal muscle-specific enhancer. Human skeletal muscle transcriptome analysis showed CELSR2 as the most differentially expressed gene (P = 1.9 × 10-7), with the RMR-lowering minor allele elevating gene expression. Experiments in mouse myoblasts confirmed enhancer-based regulation of CELSR2 expression, dependent on glucocorticoids. Rs6670347 also associated with increased oxidative phosphorylation gene expression; CELSR2 as a regulator of these genes, suggests potential influence on energy metabolism through muscle oxidative capacity. Variants in the CELSR2/PSRC1/SORT1 locus exhibit tissue-specific effects on metabolic traits, with an independent role in muscle metabolism through glucocorticoid signaling.

Diet Based on Pereskia aculeata Miller Flour Increases Muscle Volume and Modulates the Expression of Myokines in Mice Subjected to Resistance Training.

The study aimed to evaluate the effects of Pereskia aculeata Miller (ora-pro-nobis [OPN]) flour on body and biochemical parameters, thermogenic activity, and molecular expression of markers in the muscle tissue of mice subjected to resistance training (RT). Twelve mice were randomly assigned to two groups (n=6 animals/group): G1: control (Control) fed a standard diet + RT and G2: experimental (OPN) fed a diet based on OPN flour + RT. The RT consisted of a 6-week program using a vertical ladder combined with a fixed weight attached to the animal. Several parameters were measured, including assessment of body composition, biochemical markers, thermogenic activity, and molecular (mRNA expression of interleukin (IL)-6, fibronectin type III domain-containing protein 5 (FNDC5), peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α), nuclear respiratory factor 1 (NRF1), and mitochondrial transcription factor A (TFAM). The OPN group exhibited a decrease in body weight and visceral adiposity, higher energy expenditure, and lipid oxidation rate. In addition, it was observed an increase in muscle volume and in mRNA expression levels of IL-6, FNDC5, PGC-1α, and TFAM. These findings suggest that OPN flour could be a nutritional option to enhance performance in RT.

The effect of TiSi2 healing improver in self-healing ability of ceramics

A method to enhance the temperature range in which continuous self-healing fiber-reinforced ceramics (shFRCs) can self-heal is proposed to obtain a new high-temperature structural material. The effect of TiSi2 oxidation on self-healing was investigated using SiC, a typical self-healing agent, and TiSi2, which oxidizes at a lower temperature than SiC. Mixtures of SiC and TiSi2 powders were prepared by wet-mixing, and changes in their high-temperature oxidation behavior were investigated using thermogravimetry/differential thermal analysis. The oxidation of TiSi2 at 1000 °C enhanced the oxidation rate of SiC by 2–3 times. A shFRC consisting of an Al2O3 matrix, an interface layer of SiC and TiSi2, and Al2O3 fiber bundles was fabricated by slurrying and filament-winding. The strength recovery of the shFRC following three-point bending was investigated, and results indicated that the prepared material recovered 50 times faster than conventional shFRCs at 1000 °C. The self-healing improver described in this study can promote the oxidation of self-healing agents via its reaction heat. Thus, this improver may be applied as a practical component of self-healing materials.

Process Model for SiC Oxidation for a Large Range of Conditions

A comprehensive process model for 4H‐SiC oxidation is created and calibrated against a very large collection of experimental data. The model reproduces measured oxide thickness for Si‐face, C‐face, and a‐face SiC wafers, in the temperature range 950–1500 °C, in the pressure range 0.25–4.0 atm, in the thickness range 3–1600 nm, and for SiC doping ranging between 1019 cm−3 n‐type and 1019 cm−3 p‐type. The model is based on the Massoud model: Oxidation is driven by oxidants (O2, H2O) which are present in the gas phase, diffuse through the oxide, and form SiO2 at the oxide–SiC interface. For thin oxides, the interface reaction rate includes empirical correction terms which add to the oxidation rate, and which asymptotically approach zero with increasing oxide thickness. For dry oxidation, a remarkable dependence on the O2 partial pressure is discovered: For thick oxides, the oxidation rate scales linearly with the pressure, but the correction term for thin oxides scales with the square root of the pressure. This suggests that the atomistic processes responsible for the fast initial growth of oxides involve the splitting of O2 molecules into two O atoms.

High‐temperature oxidation of Cu–Al–Ni–Mn shape‐memory alloy

AbstractThe isothermal oxidation behavior of the Cu‐11.35Al‐3.2Ni‐3.5Mn (wt.%) shape‐memory alloy (SMA) in the temperature range of 500–900°C in oxygen was studied using the thermogravimetric (TG) method. TG curve showed that the alloy has parabolic isothermal oxidation characteristics. The effect of oxidation on the surface morphology and chemical composition of the Cu–Al–Ni–Mn alloy was determined by scanning electron microscopy, energy‐dispersive spectroscopy, and X‐ray photoelectron spectroscopy (XPS) analyses. The oxidation rate of SMA increases up to 700°C, remains stable at 800°C, and increases again up to 900°C. The XPS analysis identified that the corrosion products mainly contained MnO2, MnO/Mn2O3, and Al2O3.

Anisotropic Effects in Local Anodic Oxidation Nanolithography on Silicon Surfaces: Insights from ReaxFF Molecular Dynamics.

Fully understanding the anisotropic effect of silicon surface orientations in local anodic oxidation (LAO) nanolithography processes is critical to the precise control of oxide quality and rate. This study used ReaxFF MD simulations to reveal the surface anisotropic effects in the LAO through the analysis of adsorbed species, atomic charge, and oxide growth. Our results show that the LAO behaves differently on silicon (100), (110), and (111) surfaces. Specifically, the application of an electric field significantly increases the quantity of surface-adsorbed -OH2 while reducing -OH on the (111) surface, and results in a higher charge on a greater number of Si atoms on the (100) surface. Moreover, the quantity of surface-adsorbed -OH plays a pivotal role in influencing the oxidation rate, as it directly correlates with an increased formation rate of Si-O-Si bonds. During bias-induced oxidation, the (111) surface appears with a high initial oxidation rate among three surfaces, while the (110) surface underwent increased oxidation at higher electric field strengths. This conclusion is based on the analysis of the evolution of Si-O-Si bond number, surface elevation, and oxide thickness. Our findings align well with prior theoretical and experimental studies, providing deeper insights and clear guidance for the fabrication of high-performance nanoinsulator gates using LAO nanolithography.

Research on Ozone-Enhanced Oxidation of Industrial Zinc Sulfite from Flue Gas Desulfurization

ABSTRACT This study investigates the air oxidation and ozone-enhanced oxidation of zinc sulfite. Zinc sulfite was prepared by reacting pure or industrial zinc oxide with SO2 in water. The oxidation experiments were conducted under constant temperature conditions, with slurry, oxygen, and ozone concentrations in the ranges of 0.5–4%, 10–60%, and 1100–1920 ppm, respectively. The experiments involved determining the zinc ion concentration, sulfite concentration, dissolved oxygen, ozone concentration in the exhaust gas, and total organic carbon value for analysis of the oxidation process. The findings revealed that the mass transfer rate of O2 and/or O3 determined the reaction rate in the main stage of the oxidation process, while ozone affected the non-mass transfer control stage, resulting in an average enhancement of 15% in the oxidation rate. Furthermore, ozone causes organic matter attached to industrial zinc sulfite particles to fall off into the solution, significantly improving the oxidation ratio of industrial zinc sulfite.

Influence of the CYP1A2 c.-163A > C polymorphism in the effect of caffeine on fat oxidation during exercise: a pilot randomized, double-blind, crossover, placebo-controlled trial.

The aim of this study was to determine the influence of the CYP1A2 c.-163A > C (rs762551) polymorphism on the effect of oral caffeine intake on fat oxidation during exercise. Using a pilot randomized, double-blind, crossover, placebo-controlled trial, 32 young and healthy individuals (women = 14, men = 18) performed an incremental test on a cycle ergometer with 3-min stages at workloads from 30 to 70% of maximal oxygen uptake (VO2max). Participants performed this test after the ingestion of (a) placebo; (b) 3mg/kg of caffeine; (c) 6mg/kg of caffeine. Fat oxidation rate during exercise was measured by indirect calorimetry. The influence of the CYP1A2 c.-163A > C polymorphism in the effect of caffeine on fat oxidation rates during exercise was established with a three-way ANOVA (substance × genotype × intensity). Eight participants were genotyped as AA, 18 participants were CA heterozygotes, and 6 participants were CC. There was a main effect of substance (F = 3.348, p = 0.050) on fat oxidation rates during exercise with no genotype effect (F = 0.158, p = 0.959). The post hoc analysis revealed that, in comparison to the placebo, 3 and 6mg/kg of caffeine increased fat oxidation at 40-50% VO2max in AA (all p < 0.050) and 50-60% VO2max in CA and CC participants (all p < 0.050). Oral intake of 3 and 6mg/kg of caffeine increased fat oxidation rate during aerobic exercise in individuals with AA, CA and CC genotypes. This suggests that the effect of caffeine to enhance fat oxidation during exercise is not influenced by the CYP1A2 c.-163A > C polymorphism. The study was registered on clinicaltrials.gov with ID: NCT05975489.

Numerical investigation of soot formation in methane/n-heptane laminar diffusion flame doped with hydrogen at elevated pressure

The addition of hydrogen in a dual-fuel mode based on natural gas and diesel offers great potential for improving engine efficiency and reducing emissions. Therefore, detailed numerical simulations have been used to explore the effects of soot formation characteristics of natural gas-diesel dual-fuel engines doped by hydrogen at elevated pressure. Numerical simulations are compared with available experimental data, the effects of H2 addition on soot formation in laminar CH4 + n-heptane, H2 + CH4 + n-heptane, FH2 + CH4 + n-heptane diffusion flames at 2, 4, 6 and 8 atm are simulated, FH2 is added to separate the H2 chemical effects. The results show that the dilution and thermal effects of H2 inhibit soot formation, while the chemical effects of H2 promote soot formation under different pressures. The addition of H2 increases the concentration of H and OH radicals, which promotes the formation of C2H2 and benzene (A1). By simplifying the reaction path and analyzing the production rate of A1, the mechanism of H2 addition to promote A1 formation is illustrated. The concentrations of polycyclic aromatic hydrocarbon (PAH) pyrene (A4), benzo(ghi)fluoranthene (BGHIF) and benzo(a)pyrene (BAPYR) are inhibited at higher pressures that result in lower inception and condensation rates. Therefore, the increase of hydrogen abstraction acetylene addition (HACA) rate is the main reason for the increase of soot formation under chemical effects. While the O2 oxidation rate decreases and the OH oxidation rate increases, that is due to the decrease of O2 concentration and the increase of OH concentration in the soot formation area under chemical effects.

Subcritical water delamination: A promising path to efficient recycling of critical minerals

The objective of this study is to degrade the polymer layers within crystalline silicon (c-Si) photovoltaic modules and delaminate the essential valuable minerals for recycling, employing solely the thermodynamic attributes of water under subcritical conditions and abstaining from the utilization of chemical solvents. The c-Si wafer was successfully delaminated from the polymer structures at 200 °C, 100 bar for 30 min in a high-pressure reactor and ground in a planetary ball mill, where the experimental conditions were optimized for energy consumption using a Box-Behnken design. Hydrothermal subcritical delamination process provides structural changes in the polymer layers due to swelling of the ethylene vinyl acetate (EVA) and hardening of the backsheet. The energy consumption measured at the laboratory scale corresponds to the optimum response value of 0.132 kWh, demonstrating the effectiveness of the study under short-term and stable conditions.The c-Si wafer analyzed using techniques such as EDXRF, XRD, TGA, FTIR, and SEM/EDS. 87.5% Si, 1.95% aluminum, 1.12% silver, and 1.23% other metals were recovered from the solar cell. However, an oxidation rate of 6.71% by mass was detected in the c-Si wafer. The recovery rate of valuable minerals by ignoring oxidation is 98.4% of the total mass.

Tailoring oxidation resistance of Cantor alloy by addition of Ta and Al

High-entropy alloys are widely investigated for applications in the nuclear engineering field, the aerospace sector, and various other high-temperature applications. High-temperature oxidation behaviour is a typical issue in such applications. In the current work, an effort is made to tailor the oxidation behaviour of Cantor alloy (CoCrFeMnNi) in the air at 1000 °C with the addition of Ta and Al. Both CoCrFeMnNiTa as well as CoCrFeMnNiAl alloys exhibit considerable resistance to oxide scale spallation as well as develop multi-layered complex oxide scales. CoCrFeMnNiTa primarily forms rutile-type CrTaO4 oxide, which drastically reduces the inward diffusion of oxygen and nitrogen and suppresses the escape of other alloying elements. Nonetheless, the better result is obtained through the Al addition, as evidenced by the comparatively lower oxidation rate constant of CoCrFeMnNiAl in comparison to CoCrFeMnNiTa alloy. This is attributed to the superior oxidation resistance for CoCrFeMnNiAl could be related to the emergence of distinctive Cr2O3 and Al2O3 scales. Additionally, the oxide scale of CoCrFeMnNiTa was not completely smooth and showed some spallation whereas the oxide scales of CoCrFeMnNiAl remained smooth, continuous, and had stronger oxide-substrate interface adhesion.

Carbohydrate storage in cells: a laboratory activity for the assessment of glycogen stores in biological tissues.

Carbohydrates and fats constitute our primary energy sources. The importance of each of these energy substrates varies across cell types and physiological conditions. For example, the brain normally relies almost exclusively on glucose oxidation, while skeletal muscle shifts from lipids towards higher carbohydrate oxidation rates as exercise intensity increases. Understanding how carbohydrate are stored in our cells and which tissues contain significant carbohydrate stores is crucial for health professionals, especially given the role of carbohydrate metabolism in various pathophysiological conditions. This laboratory activity uses a simple and low-cost iodine binding method to quantify glycogen in mouse skeletal muscle and liver samples. By integrating the results of this activity with literature data, students can determine overall glycogen storage in the human body. The primary goal of the activity is to enhance students understanding of the importance and limitations of glycogen stores in energy metabolism.

Tailoring oxygen vacancies by synergy of dual metal cations in LaCo0.8M0.2O3 (M = Cu, Ni, Fe, Mn) towards catalytic oxidation of toluene

Enhancing the catalytic performance of transition metal oxide catalysts is prerequisite for the efficient catalytic oxidation of VOCs. Here the B-site partially substituted LaCoO3 (LaCo0.8M0.2O3, M = Cu, Ni, Fe and Mn) catalysts was synthesized for the catalytic oxidation of toluene. Among these catalysts, LaCo0.8Ni0.2O3 catalyst exhibits remarkable catalytic performance for toluene with T50 = 226 °C and T90 = 239 °C at an initial toluene concentration of 1000 ppm, whose T50 (and T90) reduced by 13 °C (and 34 °C) compared with that of LaCoO3. Confirmed by BET, XPS, and EPR characterizations, Ni substitution improves the specific surface area, Co3+/Co2+ ratio, Oads/Olatt ratio, and oxygen vacancies concentration. This improvement indicates the improvement of adsorption and activation of reactant, mobility of oxygen species, thereby contributing to the superior catalytic performance in toluene oxidation. The B-site of LaCoO3 occupied by dual cations caused the lattice distortion and formation of oxygen vacancies due to the ionic radii difference between Co and Ni cations. Moreover, the apparent activation energy of LaCo0.8Ni0.2O3, as the determining factor for the catalytic oxidation rate, was remarkably reduced. Our findings confirmed the synergy effect of Co and Ni cations at B-site on the enhancement of catalytic activity, which provides a promising strategy for oxygen vacancy engineering.

Successful operation of nitrifying granules at low pH in a continuous-flow reactor: Nitrification performance, granule stability, and microbial community

Acidic nitrification, as a novel process for treating wastewater without sufficient alkalinity, has received increasing attention over the years. In this study, a continuous-flow reactor with aerobic granular sludge was successful operated at low pH (<6.5) performing high-rate acidic nitrification. Volumetric ammonium oxidation rate of 0.4–1.2 kg/(m3·d) were achieved with the specific biomass activities of 5.8–13.9 mg N/(gVSS·h). Stable partial nitritation with nitrite accumulation efficiency over 85% could be maintained at pH above 6 with the aid of residual ammonium, whereas the nitrite accumulation disappeared when pH was below 6. Interestingly, the granule morphology significantly improved during the acidic operation. The increased secretion of extracellular polymeric substances (especially polysaccharides) suggested a self-protective behavior of microbes in the aerobic granules against acidic stress. 16S rRNA gene sequencing analyses indicated that Candidatus Nitrospira defluvii was always the dominant nitrite-oxidizing bacteria, while the dominant ammonia-oxidizing bacteria shifted from Nitrosomonas europaea to Nitrosomonas mobilis. This study, for the first time, demonstrated the improved stability of aerobic granules under acidic conditions, and also highlighted aerobic granules as a useful solution to achieve high-rate acidic nitrification.