Oxidation Process Research Articles

Influence of Chloride Ion Concentration on Corrosion Behavior of WC–MgO Composite

The influence of chloride ion (Cl−) concentration on the corrosion mechanism of WC–MgO composites has been studied in this work. The results suggest that the corrosion resistance of WC–MgO composite decreases first and then increases with the increase in Cl− concentration. Solution conductivity and dissolved oxygen content are the main influence factors. The solution conductivity determines the charge transfer process, and the dissolved oxygen determines the cathodic oxygen absorption reaction. The corrosion characteristic is typical pitting corrosion. Meanwhile, the corrosion mechanism contains an oxidation process of the WC matrix and the dissolution destruction of the MgO toughening phase. The formation of the WO3 corrosion layer hinders the general corrosion to protect the inner material. However, the dissolution of MgO induces the initiation of pitting. The local alkaline caused by MgO dissolution promotes the dissolution of the WC matrix, which leads to the expansion of pitting.

The interfacial electric field enhanced piezo-catalytic performance of Bi2S3/Ni/CN composites for peroxymonosulfate activation advanced oxidation processes (AOP) systems

The interfacial electric field of Bi2S3/Ni/CN composites has been found to enhance the piezo-catalytic performance in peroxymonosulfate activation for advanced oxidation processes (AOP) systems. This novel research field aims to strengthen AOP systems for pollutant control and degradation through the utilization of the piezo-catalysis. In this particular study, a hammer coral-like Bi2S3/Ni/CN composite with interfacial electric field was synthesized by incorporating bismuth sulfide into the Ni/CN matrix. The efficient separation of piezoelectric carriers and charge transfer between nickel and bismuth in the resulting Bi2S3/Ni/CN composite facilitate a synergistic effect in the activation of peroxymonosulfate (PMS). It has been observed that, when subjected to ultrasound, this composite can achieve a degradation rate exceeding 90% within a minute towards Rh B as a model dye. Notably, the degradation process is primarily driven by piezoelectric hole and mono-linear oxygen non-free radicals. Additionally, the interfacial electric field facilitates valence electron transfer and ultimately enhancing reaction efficiency. Experimental results further demonstrate that the removal efficiency of organic pollutants can surpass 98% within a pH range of 1–9 over a duration of 3 min, demonstrating wide pH response range and high catalytic activities.

Transformation of metoprolol in UV/PDS process: Role and mechanisms of degradation and polymerization

Advanced oxidation processes for the treatment of organic pollutants in wastewater suffer from difficulties in mineralization, potential risks of dissolved residues, and high oxidant consumption. In this study, radical-initiated polymerization is dominated in an UV/peroxydisulfate (PDS) process to eliminate organic pollutant of pharmaceutical metoprolol (MTP). Compared with an ideal degradation-based UV/PDS process, the present process can save four fifths of PDS consumption at the same dissolved organic carbon removal of 47.3%. Simultaneously, organic carbon can be recovered from aqueous solution by separating solid polymers at a ratio of 50% of the initial chemical oxygen demand. The chemical structure of products was analyzed to infer the transformation pathways of MTP. Unlike previous studies on simple organic pollutants that the polymerization can occur independently, the polymerization of MTP is dependent on the partial degradation of MTP, and the main monomer in polymerization is a dominant degradation product (4-(2-methoxyethyl)-phenol, denoted as DP151). The separated solid polymers are formed by repeated oxidation and coupling of DP151 or its derivatives through a series of intermediate oligomers. This proof-of-concept study demonstrates the advantage of polymerization-dominated mechanism on dealing with large organic molecules with complex structures, as well as the potential of UV/PDS process for simultaneous organic pollution reduction and organic carbon recovery from aqueous solution.

Green mechanochemical activation of solid persulfate to remove PAHs in soil: Performance and mechanism

Due to the high biotoxicity and persistence of polycyclic aromatic hydrocarbons (PAHs), the remediation of PAHs-contaminated soil becomes an intractable problem. Persulfate-based advanced oxidation processes are widely used to degrade PAHs in aquatic environment. However, they are not convenient for used in soil due to the heterogeneity and complexity of soil matrix. In this study, a green and convenient ball milling process is introduced to activate persulfate for the remediation of PAHs-contaminated soil. About 82.5% PAHs were removed with 10% wt. Na2S2O8 (PS) addition and ball-milling for 2 h under 500 r/min. The degradation of PAHs is attributed to the attack of radicals (SO4·- and·OH) generated from the activation of PS by mechanochemistry. Moreover, stable Si-O bonds were disrupted during ball-milling process, and formed free electron on the surface of soil particles. This facilitates the electron transfer from oxidants to contaminants. The particle size, surface element composition, functional group, and thermogravimetric analysis confirmed the slight disturbance of ball-milling-assisted PS process on the physical and chemical properties of soil. Therefore, ball-milling assisted PS approach would be a promising technology for the remediation of PAHs-contaminated soil.

Synthesis, Surface Modification and Magnetic Properties Analysis of Heat-Generating Cobalt-Substituted Magnetite Nanoparticles.

Here, we present the results of the synthesis, surface modification, and properties analysis of magnetite-based nanoparticles, specifically Co0.047Fe2.953O4 (S1) and Co0.086Fe2.914O4 (S2). These nanoparticles were synthesized using the co-precipitation method at 80 °C for 2 h. They exhibit a single-phase nature and crystallize in a spinel-type structure (space group Fd3¯m). Transmission electron microscopy analysis reveals that the particles are quasi-spherical in shape and approximately 11 nm in size. An observed increase in saturation magnetization, coercivity, remanence, and blocking temperature in S2 compared to S1 can be attributed to an increase in magnetocrystalline anisotropy due to the incorporation of Co ions in the crystal lattice of the parent compound (Fe3O4). The heating efficiency of the samples was determined by fitting the Box-Lucas equation to the acquired temperature curves. The calculated Specific Loss Power (SLP) values were 46 W/g and 23 W/g (under HAC = 200 Oe and f = 252 kHz) for S1 and S2, respectively. Additionally, sample S1 was coated with citric acid (Co0.047Fe2.953O4@CA) and poly(acrylic acid) (Co0.047Fe2.953O4@PAA) to obtain stable colloids for further tests for magnetic hyperthermia applications in cancer therapy. Fits of the Box-Lucas equation provided SLP values of 21 W/g and 34 W/g for CA- and PAA-coated samples, respectively. On the other hand, X-ray photoelectron spectroscopy analysis points to the catalytically active centers Fe2+/Fe3+ and Co2+/Co3+ on the particle surface, suggesting possible applications of the samples as heterogeneous self-heating catalysts in advanced oxidation processes under an AC magnetic field.

Mechanical insights into desulfurization by peroxymonosulfate oxidation via a non-reactive oxygen species pathway

Air pollution by sulfur dioxide (SO2) remains a pressing concern for both the environment and human health. Desulfurization enhanced by persulfate based advanced oxidation processes (PS-AOPs) has been proven to be a feasible method. However, the inherent contradiction between the rapid diffusion mass transfer of SO2 in the “gas-liquid-gas” phase and the limited lifespan of reactive oxygen species (ROS) can not be ignored. Excessive investment in PS is required to sustainably generate ROS to achieve continuous desulfurization performance, which may lead to excessive PS consumption. To address this issue, whether PS can achieve the oxidation absorption of SO2 via a non-reactive oxygen species pathway was investigated. Experimental and computational results demonstrated that peroxymonosulfate (PMS) instead of peroxydisulfate (PDS) had a great SO2 removal performance, the utilization of PS could be effectively achieved by maintaining a 1:1 molar ratio of PMS and removed SO2. The presence of HOO bonds in the PMS introduced a partial positive charge to the oxygen atom, making the PMS polar and more susceptible to be attacked by the nucleophile HSO3-. So SO2 underwent a series of processes including dissolution, dissociation, one-oxygen atom transfer, and ionization before ultimately being converted into SO42- ions, effectively achieving its removal from flue gas. This study may presents a novel approach for achieving high-efficiency flue gas desulfurization.

Electrochemically-Driven 1,4-Aryl Migration via Radical Fluoromethylation of N-allylbenzamides: a Straightforward Access to Functionalized β-Arylethylamines.

An electrochemical radical Truce Smiles rearrangement of N-allylbenzamides is documented herein. The selective 1,4-aryl migration was triggered by the radical fluoromethylation of the alkene providing a direct route to fluoro derivatives of the highly privileged β-arylethylamine pharmacophore. This practical transformation utilizes readily available starting materials and employs an electrical current to drive the oxidative process under mild reaction conditions. It accommodates a variety of migratory aryl groups with different electronic properties and substitution patterns. Careful selection of the protecting group on the nitrogen atom of the N-allylbenzamide is crucial to outcompete the undesired 6-endo cyclization and achieve high level of selectivity towards the 1,4-aryl migration. DFT calculations support the reaction mechanism and unveil the origin of selectivity between the two competitive pathways.

Endogenous advanced oxidation process with peracetic acid for recycling spent LiFePO4 batteries

LiFePO4 batteries are becoming more widely used due to their low cost and high stability advantages, which means that many spent batteries are generated. Designing green and efficient recycling methods for used batteries is strategically significant for the sustainable development of the new energy industry. This study innovatively proposes a self-activated advanced oxidation process with peroxyacetic acid for recycling spent LiFePO4, selectively releasing Li+ while converting LiFePO4 to FePO4. Quenching tests show that the de-embedding of Li+ is mainly caused by the rapid attack from HO• and R-O• radicals. Furthermore, the recycled products Li2CO3 and FePO4 are employed to regenerate LiFePO4 cathode materials, forming a closed-loop recycling process. Compared with traditional hydrometallurgy and hydrogen peroxide oxidation methods, this technology has obvious advantages in terms of process complexity, energy consumption, reagent consumption, recovery profit, and environmental friendliness. This work opens up a new way for the recycling of spent lithium-ion batteries.

α‐MnO2/RuO2 Heterostructure‐Modified Polypropylene Separator for High‐Performance Lithium–Sulfur Battery

AbstractLithium–sulfur (Li–S) battery is a promising next‐generation energy storage system. However, the poor cyclability caused by the shuttle effect is still a key challenge for its practical application. Here, a polypropylene separator modified with α‐MnO2/RuO2 heterostructure is presented to facilitate the transformation of lithium polysulfides (LiPSs) and optimize the rate‐determining step in both the reduction and oxidation processes of the sulfur electrode. The unique separator effectively suppresses the dissolution and shuttling of soluble LiPSs in Li–S batteries. The α‐MnO2/RuO2 heterostructure modified separator with a Ru content of ≈8 wt% enables a high areal capacity of over 5.0 mAh cm−2 after 55 cycles at 0.2C in a Li–S coin cell, and the resultant pouch cell retains 78.2% of its initial capacity after 200 cycles at 0.1C, suggesting considerable potential for commercial applications. This work provides new insights into the regulation of electrochemical reactions in Li–S batteries.

Anemia and Fatigue in Patients with Chronic Kidney Failure

Chronic renal failure results in impaired kidney function, effectively eliminating metabolic waste and regulating fluid and electrolyte balance. The accumulation of waste metabolites is thought to impact the occurrence of anemia and fatigue. However, no research has shown a correlation between the incidence of anemia and fatigue in sufferers of chronic kidney failure. This study aimed to evaluate the relationship between hemoglobin levels and the degree of fatigue experienced by individuals diagnosed with chronic kidney disease. This research uses a cross-sectional study approach. The study population consisted of patients with chronic kidney failure at one of the hospitals in Lumajang Regency who were identified by the indicator of high BUN values. The sample size for this research was 50 people selected through purposive sampling. The data type used is primary data, with the independent variable being the Hb value, while the dependent variable is the level of fatigue in chronic kidney failure patients. The results of the Pearson correlation test in this study showed that there was a significant relationship between the percentage of hemoglobin levels in the blood and the level of fatigue in chronic kidney failure patients (p-value = <0,000; α = 0.05), with a strength of relationship 0,6092 which means the level Hemoglobin in the blood and the level of fatigue have a perfect degree of correlation. In patients with chronic renal failure and low hemoglobin levels, their fatigue levels will become more severe. Insufficient hemoglobin levels lead to a reduced count of red blood cells, causing a decline in the body's capacity to transport oxygen. This inadequate oxygen supply hampers the oxidation process and energy production in the form of ATP within the body's cells. Consequently, patients with chronic renal failure may undergo a substantial decrease in energy levels and experience significant tiredness.

Sustainable Development in Dye Waste Managemen : A Comparative Study on the Effectiveness of Adsorption and γ-Radiolysis

Pyrromethene 567 (PM567), a BODIPY class of dye; is widely used in medicine, chemistry, material science, and high-power dye lasers. During its use, PM567 dye waste is generated in ethanol solvent which needs to be treated before its disposal. In our study, we -radiolysis, an advanced oxidation process (AOP), and adsorption, a simple and easy option. Interestingly, -radiolysis were not efficient for dye effluent treatment in organic solvents. This inefficiency was attributed to competing reactions leading to the scavenging of dye-degrading radicals. -dose rate (3.5 kGy) feasible in the system; 62% is the maximum removal efficiency achieved by this method. For a comparison, we also investigated the adsorption efficiency of PM567 dye from ethanol solvent using commercially available adsorbents. Among these, powdered activated carbon (PAC) demonstrated the highest removal efficiency, reaching 95%, much higher than that of -radiolysis method. In line with the pursuit of sustainable development, we synthesized granular activated carbons (AC1, AC2, AC3) from coconut shells, a lignocellulosic biowaste. The characterization of these carbons revealed that AC3, with a higher iodine value and CCl4 activity, possessed a systematic pore structure (SEM analysis), a larger specific surface area (1708 m2 .g-1), and a higher micro-pore volume (0.61 cc.g-1). AC3 hence, emerged as the most effective adsorbent, achieving 95% efficiency comparable to PAC.

Experimental Design of the Adhesion between a PEI/Glass Fiber Composite and the AA1100 Aluminum Alloy with Oxide Coating Produced via Plasma Electrolytic Oxidation (PEO)

In this study, the AA1100 aluminum alloy underwent the plasma electrolytic oxidation (PEO) process to enhance its adhesion to a thermoplastic composite of polyetherimide (PEI) reinforced with glass fiber, following ASTM D1002:10 standards. A 23 factorial design was employed, varying three parameters in the oxidation process: immersion time, applied electric potential, and electrolyte concentration (Na2B4O7). The joining of aluminum and thermoplastic composite samples was achieved through oxy-fuel welding (OFW), using oxygen and acetylene gases. For the characterization of the joined samples, a universal tensile testing machine was utilized with a displacement speed of 1.5 mm/min. The analysis of the oxide coating involved scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and Fourier transform infrared spectroscopy (FT-IR). Through variance analysis, it was determined that the statistical model encompasses approximately 80% of the variability in the adhesion process between materials. An improvement of up to 104% in adhesion between the materials was observed with the process, indicating an effective bond due to the presence of the thermoplastic matrix in the treated aluminum sample. This improvement is attributed to the morphology of the oxide coating, resembling corals, with micro-pores and recesses that facilitated mechanical anchoring.

Consumer Satisfaction and Perception Towards Green Tea

Green tea is a type of tea that is made from Camellia sinensis leaves and buds that have not undergone the same withering and oxidation process used to make oolong teas and black teas.[1] Green tea originated in China, but its production and manufacture has spread to other countries in East Asia. Several varieties of green tea exist, which differ substantially based on the variety of C. sinensis used, growing conditions, horticultural methods, production processing, and time of harvest. Although there has been considerable research on the possible health effects of consuming green tea regularly, there is little evidence that drinking green tea has any effects on health

L-proline Interaction with Methyl Linoleate Oxidation Products Formation in Dry System and at Temperatures: For Understanding in Low-Moisture Foods

Dry and low-moisture foods could experience a significant loss in nutritional value due to the process of methyl linoleate oxidation. L-proline could interact with lipid oxidation products, potentially modifying their formation and reaction path. However, there was a lack of research on the interaction between L-proline and methyl linoleate oxidation products in dry and low-moisture food matrices, which was a concern given the potential impact on food safety and nutrition. To address this knowledge gap, a study investigated the interaction between L-proline and the oxidation products of methyl linoleate in a dry system. The study examined the formation of methyl linoleate oxidation products such as conjugated dienes, hydroperoxide, and hexanal in the absence and presence of varying moles of L-proline at different temperatures. The formation of conjugated diene, hydroperoxide, and hexanal was analyzed using UV spectrometer analysis, xylenol orange, and DNPH derivatization HPLC-UV analysis. The results showed that adding proline to methyl linoleate samples stabilized conjugated diene and decreased hydroperoxide and hexanal levels as temperature increased, compared to the control sample. This suggests that L-proline effectively interacted with methyl linoleate oxidation products and altered their formation and oxidation path in the dry system. Overall, this study provided a basis for significantly enhancing understanding of the reactions between L-proline and methyl linoleate oxidation products in dry and low-moisture foods, offered practical implications for the food industry, and paved the way for future research.

Process and mechanism of preparing metallized blast furnace burden from metallurgical dust and sludge

Metallurgical dust and sludge are solid waste resources with recycling value. In recent years, rotary hearth furnace has become the most important means to treat metallurgical dust and sludge because of its wide range of raw materials and strong treatment capacity. In this study blast furnace ash and converter sludge were selected as the research objects, and high-quality metallized pellets were prepared based on the rotary hearth furnace process. The strength changed of pellets, the reduction process of iron oxides and the removal process of zinc during the roasting of pellets in rotary hearth furnace were studied. To explore the reasonable roasting condition for preparing metallized pellets in rotary hearth furnace. The optimum roasting temperature of the pellets was 1250℃ and the roasting time was 25 min. The compressive strength, metallization rate and dezincification rate of metallized pellets reached 1361N, 97.44% and 95.67%, respectively. The efficient resource utilization of various metallurgical dust and sludge is realized.

Cellular and Mitochondrial Pathways Contribute to SGLT2 Inhibitors-mediated Tissue Protection: Experimental and Clinical Data.

In metabolic syndrome and diabetes, compromised mitochondrial function emerges as a critical driver of cardiovascular disease, fueling its development and persistence, culminating in cardiac remodeling and adverse events. In this context, angiotensin II - the main interlocutor of the renin-angiotensin-aldosterone system - promotes local and systemic oxidative inflammatory processes. To highlight, the low activity/expression of proteins called sirtuins negatively participates in these processes, allowing more significant oxidative imbalance, which impacts cellular and tissue responses, causing tissue damage, inflammation, and cardiac and vascular remodeling. The reduction in energy production of mitochondria has been widely described as a significant element in all types of metabolic disorders. Additionally, high sirtuin levels and AMPK signaling stimulate hypoxia- inducible factor 1 beta and promote ketonemia. Consequently, enhanced autophagy and mitophagy advance through cardiac cells, sweeping away debris and silencing the orchestra of oxidative stress and inflammation, ultimately protecting vulnerable tissue from damage. To highlight and of particular interest, SGLT2 inhibitors (SGLT2i) profoundly influence all these mechanisms. Randomized clinical trials have evidenced a compelling picture of SGLT2i emerging as game-changers, wielding their power to demonstrably improve cardiac function and slash the rates of cardiovascular and renal events. Furthermore, driven by recent evidence, SGLT2i emerge as cellular supermolecules, exerting their beneficial actions to increase mitochondrial efficiency, alleviate oxidative stress, and curb severe inflammation. Its actions strengthen tissues and create a resilient defense against disease. In conclusion, like a treasure chest brimming with untold riches, the influence of SGLT2i on mitochondrial function holds untold potential for cardiovascular health. Unlocking these secrets, like a map guiding adventurers to hidden riches, promises to pave the way for even more potent therapeutic strategies.

Designing ammonia oxidation catalysts via physical mixing of Pt/SiO2 and Cu/ZSM-5

Ammonia (NH3) is emerging as a carbon-neutral fuel alternative; however, its use poses environmental and health risks due to NH3 slip. The NH3-selective catalytic oxidation (NH3-SCO) process, which converts NH3 into N2 and H2O, offers a solution. However, it faces challenges with respect to the formation of byproducts, particularly N2O and NOx. This study focuses on designing NH3-SCO catalysts to enhance low temperature NH3 conversion efficiency while minimizing undesired byproducts. Pt/SiO2 catalysts were synthesized with adjusted Pt particle sizes to improve the NH3-SCO activity and were physically mixed with Cu/ZSM-5 to overcome the low N2 selectivity of Pt-based catalysts by utilizing the selective catalytic reduction (SCR) ability of Cu/ZSM-5. Pt1Cu3 catalyst, a physical mixture of Pt/SiO2 and Cu/ZSM-5 in a 1:3 mass ratio, was found to be the most effective, achieving complete NH3 oxidation at 250 ℃ while maintaining a high N2 selectivity of approximately 80%. Further investigation revealed that the performance of the Pt1Cu3 catalyst was significantly influenced by the arrangement and physical proximity of the Pt/SiO2 and Cu/ZSM-5 catalysts, with a closely contacted mixture showing synergistic effects that enhanced activity and selectivity. These results suggest that the Pt1Cu3 catalyst offers a promising solution for NH3 emission control by utilizing a balanced approach that combines SCO and SCR reactions.

Exploring Reversible Redox Behavior in the 6H-BaFeO3-δ (0 < δ < 0.4) System: Impact of Fe3+/Fe4+ Ratio on CO Oxidation.

This work is devoted to evaluating the relationship between the oxygen content and catalytic activity in the CO oxidation process of the 6H-type BaFeO3-δ system. Strong evidence is provided about the improvement of catalytic performance with increasing Fe average oxidation state, thus suggesting the involvement of lattice oxygen in the catalytic process. The compositional and structural changes taking place in both the anionic and cationic sublattices of the catalysts during redox cycles have been determined by temperature-resolved neutron diffraction. The obtained results evidence a structural transition from hexagonal (P63/mmc) to orthorhombic (Cmcm) symmetry. This transition is linked to octahedra distortion when the Fe3+ concentration exceeds 40% (δ values higher than 0.2). The topotactical character of the redox process is maintained in the δ range 0 < δ < 0.4. This suggests that the cationic framework is only subjected to slight structural modifications during the oxygen exchange process occurring during the catalytic cycle.

Role of Reactive Oxygen Species in the Pathogenesis of Bronchial Asthma and Obstructive Pulmonary Diseases: Systematic Review

The article discusses the role of reactive oxygen species (ROS) in the pathogenesis of bronchial asthma and obstructive pulmonary diseases. The review follows a structured approach beginning with a comprehensive search of electronic databases, then findings from the included studies were summarized and used to draw comprehensive conclusions. The authors state that increased activity of oxidative processes and insufficient activity of the antioxidant system lead to the accumulation of ROS in the respiratory tract. This leads to direct damage to epithelial cells, activation of inflammatory cells, and stimulation of inflammatory mediators. ROS also activate transcription factors that increase inflammation and airway obstruction. Thus, maintaining the balance of the oxidant-antioxidant system is an important strategy for the treatment of these diseases.Keywords: Reactive oxygen species; Bronchial asthma; Chronic obstructive pulmonary disease; Oxidative stress; Antioxidant system

Cobalt-Modified Black Phosphorus Nanosheets-Enabled Ferrate (VI) Activation for Efficient Chemiluminescence Detection of Thiabendazole.

The development of chemiluminescence-based innovation sensing systems and the construction of a sensing mechanism to improve the analytical performance of compounds remain a great challenge. Herein, we fabricated an advanced oxidation processes pretreated chemiluminescence (AOP-CL) sensing system via the introduction of cobalt-modified black phosphorus nanosheets (Co@BPNs) to achieve higher efficient thiabendazole (TBZ) detection. Co@BPNs, enriched with lattice oxygen, exhibited a superior catalytic performance for accelerating the decomposition of ferrate (VI). This Co@BPNs-based ferrate (VI) AOP system demonstrated a unique ability to selectively decompose TBZ, resulting in a strong CL emission. On this basis, a highly selective and sensitive CL sensing platform for TBZ was established, which exhibited strong resistance to common ions and pesticides interference. This was successfully applied to detecting TBZ in environmental samples such as tea and kiwi fruits. Besides, the TBZ detection mechanism was explored, Co@BPNs-based ferrate (VI) AOP system produced a high yield of ROS (mainly 1O2), which oxidized the thiazole-based structure of TBZ, generating chemical energy that was transferred to Co@BPNs via a chemical electron exchange luminescence (CIEEL) mechanism, leading to intense CL emission. Notably, this study not only proposed an innovative approach to enhance the chemical activity and CL properties of nanomaterials but also offered a new pathway for designing efficient CL probes for pollutant monitoring in complex samples.