Free Radical Attack Research Articles

Green tea (Camellia sinensis L.) potential to liver of hyperuricemia rats (Rattus norvegicus) fed with high purine diet

Uric acid is produced in tissues containing xanthine oxidases, like the small intestine and liver, as involved in the purine metabolism of adenine and guanine. High uric acid levels cause damage to cell membranes due to the lipid peroxidase chain reaction. Foods containing high purines will activate the xanthine oxidase (XOD), causing an increase in free radicals. Free radicals attack polyunsaturated fatty acids (PUFA) by forming lipid peroxides. PUFA molecules contain multiple double bonds, which make them susceptible to oxidation by reactive oxygen species (ROS), such as free radicals. PUFA will be broken into simple compounds such as pentane, ethane, and aldehydes, leading to malondialdehyde (MDA) formation. High MDA levels illustrate the process of cell membrane oxidation leading to cell membrane damage. Hyperuricemia is often treated using synthetic drugs such as allopurinol; however, it can cause side effects. Some people will choose medicinal plants with minimal side effects. Green tea (Camellia sinensis L.) contains many polyphenol antioxidants, especially flavonoids, which also have a strong antioxidant effect by exerting multiple mechanisms such as inhibiting several enzymes, including antiphospholipid peroxidase, free radical scavengers, metal bonds, and xanthine oxidase (XOD). Statistical analysis results proved that green tea with a dose of 600 mg/kg BW could decrease the level of MDA in the liver by 84.87% (p 0.01) and reduce the activity of XOD by 35.36% (p 0.01). Taken together, green tea can improve liver histopathology.

Protective effects of Khaya senegalensis stem bark extracts against acetaminophen-induced oxidative damage, dyslipidaemia, and hepatotoxicity in rats

Background Free radical attacks have been implicated in the aetiology of many diseases and several plants are used traditionally for the management of many oxidative-stress related diseases. Khaya senegalensis is used traditionally for the management diseases such as diabetes and for the treatment of infections. However, mechanisms underlying actions of K. senegalensis are poorly understood. Purpose This study aimed at the preliminary determination of the phytochemical constituents and investigation of the antioxidative and hepatoprotective actions of K. senegalensis in acetaminophen-treated rats. Method Aqueous extracts of K. senegalensis were screened for the presence of key phytochemicals. Total flavonoid and phenolic contents were quantified. Wistar albino rats were pre-treated with saline (control) or graded concentrations of K. senegalensis (50 – 200mg/kgbw) for 10 days prior to acetaminophen (2g/kg body weight) administration. Serum levels of vitamin C, thiobarbituric reactive substances, catalase activities, enzyme markers of liver function were assessed. Cholesterol-phospholipid ratio in treated-rats were determined. Results K. senegalensis extract showed the presence of saponins, tannins, cardiac glycosides, alkaloids, flavonoids and phenolic compounds. Total phenolic and total flavonoid contents were determined as 57.14±0.85mgQE/g and 51.72±0.77mgGE/g. Acetaminophen (2g/kg bw) raised serum TBARS (4.7-fold, P<0.001), H2O2 levels (2.3-fold, P<0.001), AST (5.9-fold, P<0.001), ALT (6.6-fold, P<0.001) and ALP (4.2-fold, P<0.001) and reduced serum levels of vitamin C (54%, P<0.001) and catalase activity (74.6%, P<0.001). Treatment of K. senegalensis extracts inhibited effects of acetaminophen on TBARS (18.2% - 46.4%, P<0.05 – 0.001), vitamin C (1.4 – 1.8-fold, P<0.001 – 0.05), H2O2 levels (19.1 – 50.1%, P<0.001-0.05), catalase activities (1.4 – 3.1-fold, P<0.001 – 0.05), AST (27.7 – 62.8%, P<0.001 – 0.05), ALT (35.6 – 57.5%, P<0.001 – 0.05) and ALP (15.9 – 46.2%, P<0.01 – 0.05). The extract reduced cholesterol-phospholipid ratio (21 – 31%, P<0.05). Conclusion These results motivate further development of the therapeutic potential of K. senegalensis

Efficient degradation of tetracycline by cobalt ferrite modified alkaline solution nanofibrous Ti3C2Tx MXene activated peroxymonosulfate system: Mechanism analysis and pathway

Magnetic CoFe2O4 nanoparticles have received considerable attention as an activator for peroxymonosulfate (PMS) in the degradation of tetracycline. However, it is still challenging to construct CoFe2O4 composites with good dispersion and highly exposed reactive sites. Herein, the KOH fiber-functionalized MXene matrix decorated by cobalt ferrite nanoparticles (denoted as CoFe2O4@Alk-MXene) was developed by electrostatic self-assembly method. The layered fibrotic structure effectively disperses and fixes cobalt ferrite nanoparticles, increasing the exposure of reactive sites. The as-prepared CoFe2O4@Alk-MXene material exhibited rapid removal of 100% tetracycline hydrochloride (TC-HCl) within 10 minutes by activating PMS, leveraging the excellent conductivity of alkalized MXene and the efficient activation of transition metal atoms. The experimental and theoretical analysis revealed that the electron transfer process of Ti2+/Ti4+, Co2+/Co3+ and Fe3+/Fe2+, as well as the free radical and non-free radical attack behaviors produced by the adsorption of PMS by the composite, are the primary mechanisms for achieving rapid removal of pollutants. A comprehensive degradation mechanism and potential pathways were proposed based on these findings. Overall, CoFe2O4@Alk-MXene/PMS emerges as a promising catalytic system for TC removal.

Exploring boratrane's potential to enhance the thermal stability of phenol-formaldehyde resins by borate bridge as a crosslinker and the mechanistic formation of boron species in carbonaceous materials: A comprehensive study

In advanced material science, we explore the potential of boratrane, a promising agent for enhancing thermal stability. By combining rigorous Density Functional Theory (DFT) calculations with groundbreaking experimental analyses, we reveal the intricate interplay of radical intermediates and mechanisms underlying the thermal evolution of boratrane-infused materials. Our innovative approach illuminates dynamic structural transformations and elucidates boratrane's pivotal role in fortifying thermal resilience. The DFT calculations identify radical intermediates and mechanisms of thermal degradation, highlighting the role of borate bridges in delocalizing π-electrons in aromatic rings through Gibbs free energy (∆GRXN), Highest Occupied Molecular Orbital (HOMO), Lowest Unoccupied Molecular Orbital (LUMO), and electrostatic potential (ESP) analyses. Fukui function analysis provides insights into the reactivity of these structures towards free radical attacks. Our findings demonstrate that boratrane-modified resins exhibit a stable BO4- structure, which prevents self-condensation of boratrane to B2O3 and enhances the thermal stability of oxygenated resins. This improvement is due to the formation of intramolecular hydrogen bonds, contributing to helix-like structures that strengthen the resin. The mechanism by which the BO4- structure terminates radical agents and transforms into carbonaceous material is elucidated through thermodynamic values, revealing the plausible reactions and chemical structure of boron in the resulting material.

Catalytic pyrolysis of biomass waste using montmorillonite-supported ultrafine iron nanoparticles for enhanced bio-oil yield and quality

The catalytic fast pyrolysis process is a promising method for converting biomass waste into bio-oil, where the catalyst plays a crucial role in determining the yield and quality of the products. In this study, ultrafine iron nanoparticles were incorporated onto a montmorillonite substrate through the pyrolyzing coordinated polymer method to enhance liquid fuel production via catalytic pyrolysis of biomass waste. The catalyst showed a uniform distribution of iron on the montmorillonite surface, indicating that the incorporation was successful. Catalytic pyrolysis led to an increase in liquid yields and a decrease in gas product yields compared to direct pyrolysis. The highest bio-oil yield obtained was 56.9% during the catalytic pyrolysis of corncob, which was found to be particularly well-suited for the production of bio-oil. Furthermore, the proposed reaction pathway was based on identifying the composition of the bio-oil, which was further supported by quantum chemical calculations of chemical bond strength and the likelihood of free radical attacks. These findings demonstrate the potential of using montmorillonite-supported ultrafine iron nanoparticles to enhance bio-oil yield and quality in biomass pyrolysis processes.

Employing lattice compression spin polarization electric field for boosting degradation of mixed antibiotics in wastewater

Localized polarization electric field is a key factor affecting photocatalytic activity. In this study, the localized polarization electric field of lattice strain was introduced into the electronic structure of Bi2WO6 by using the high and low valence state doping method. The impurity energy level induced by lattice strain further affects the gap energy level. As an intermediate state for electron transfer, the gap level further promotes the dynamics of photo generated charges, reducing the band gap by 0.4 eV and improving the photoelectric performance by 60 %. Various tests and theoretical calculations have confirmed that the internal electric field of local polarization significantly improves the generation and transfer rate of photo-generated charges, thereby boosting catalytic activity. The removal ratios of ciprofloxacin (CIP) and tetracycline (TC) in the mixed wastewater reach 91.5 % and 97.1 % in 90 min, respectively. Cyclic tests have shown that the electronic structure control exhibits excellent stability with removal ratios of CIP and TC of 83.9 % and 85.7 %, respectively. Finally, the 8C of CIP and the 11C and 19O of TC are most susceptible to the attack of free radicals generated by lattice compression spin polarization electric fields based on the theoretical calculations of the Fukui function and the analysis of intermediates. This work provides new insights into the design of catalysts for efficient photo generated charge dynamics with lattice strain.

Unveiling the fate of metal leaching in bimetal-catalyzed Fenton-like systems: pivotal role of aqueous matrices and machine learning prediction

Metal-based catalytic materials exhibit exceptional properties in degrading emerging pollutants within Fenton-like systems. However, the potential risk of metal leaching has become pressing environmental concern. This study addressed scientific issues pertaining to the leaching behavior and control strategies for metal-based catalytic materials. Innovative cobalt-aluminum hydrotalcite (CoAl-LDH) triggered peroxymonosulfate (PMS) activation system was constructed and achieved near-complete removal of Ciprofloxacin (CIP) across diverse water quality environments. Notably, it was found that the tunable ion exchange and Al3+ stabilization of CoAl-LDH occurred due to the particularity of neutral water quality, resulting in significantly lower Co2+ leaching levels (0.321 mg/L) compared to acidic conditions (5.103 mg/L). In light of this, machine learning technology was then employed for the first time to simulate the dynamic trend of Co2+ leaching and elucidated the critical regulatory roles and mechanisms of Al3+, aqueous matrix, and reaction rate. Furthermore, degradation systems based on different water quality and metal leaching levels regulated the generation levels of SO4.- and O2∙-, and the unique advantages of free radical attack paths were clarified through CIP degradation products and ecotoxicity analysis. These findings introduced novel insights and approaches for engineering application and pollution control in metal-based Fenton-like water treatment.

The Effectiveness of Vitamin E Soft Capsules as an Antioxidant

Antioxidants inhibit the oxidation of other molecules and play an important role in maintaining a healthy body. Antioxidants are found in fruits, vegetables, all parts of plants, and are present in the body as enzymes or products of metabolism. Vitamin E refers to a large number of natural or synthetic compounds, with alpha-tocopherol being the most active and widely distributed form in nature. Alpha-tocopherol is the most active antioxidant form of vitamin E and serves as the primary lipophilic antioxidant in plasma, membranes, and tissues. The most important function of vitamin E is its antioxidant capability, counteracting free radical attacks that can damage cells and cause various degenerative diseases. Additionally, antioxidants help reduce the effects of photoaging on the skin, potentiate anti-aging and anti-inflammatory activity, increase the rate of wound healing, and help maintain healthy eyes and the immune system. One form of vitamin E dosage form is a soft capsule which has several advantages, including the ease of filling the Active Pharmaceutical Ingredient (API) in liquid form, higher production capacity and formulation uniformity compared to gelatin tablets or hard capsules. Soft capsule preparations also have rapid API release, which can result in achieving therapeutic blood levels more quickly and achieving greater bioavailability. This study aims to evaluate soft capsule dosage forms in enhancing the effectiveness of vitamin E as an antioxidant. The research utilizes review articles sourced from national and international journals, as well as scientific journals. The results show that vitamin E supplementation in soft capsules can increase its effectiveness as an antioxidant.

Quantification of phenol degradation using hydrodynamic cavitation‐based packed bed reactor based on glass balls

AbstractThe current study presents a novel and effective cavitation technique for the degradation of phenol using a hydrodynamic cavitation‐based packed bed reactor (HCPBR). Several operational parameters, including fluid velocity, hydrogen peroxide (H2O2) generation (18.06 μM of H2O2 in 60 min), and initial phenol concentration, have been studied using a HCPBR. The effective parameters for phenol degradation were found to be a fluid velocity of 85.15 m/s and an initial phenol concentration of 20 ppm. It was also noted that the presence of a glass marble‐bed (15.35%) in the cavitation reactor exhibits a substantial effect on the degradation of phenol compared to the absence of a glass marble‐bed (2.91%). The investigation also examined the effect of combining hydrodynamic cavitation with chemical oxidation processes, specifically H2O2, persulfate (Na2S2O8 and K2S2O8), and titanium dioxide, on the extent of phenol degradation. Persulfate was shown to have a significant effect on phenol degradation at 1 g/L. To clarify if free radical attack is the driving force behind degradation, the impact of radical scavengers such as n‐butanol has also been examined. Toxicological assessments revealed that, for lentil meristematic cells, the therapy was quite cytotoxic, but it needs to be improved to eliminate its genotoxic side effects. Overall, the experiment clearly demonstrated the effectiveness of the HCPBR for phenol degradation.

Sunlight degradation of tetracycline by Z-type BiOI/g-C3N4 photocatalyst synthesized via a simple two-step process: Response surface methods, degradation pathways, toxicity evaluation

A method combining grinding and hydrothermal treatments was utilized to densely load three-dimensional BiOI onto two-dimensional g-C3N4, thereby preparing a BiOI/g-C3N4 photocatalyst with a Z-type heterojunction. Under varying climatic conditions throughout the year, 10%BiOI/g-C3N4 photocatalyst degraded 92.26 % of tetracycline (TC) under sunlight exposure in summer (sunny days) in 150 min, whereas it only degraded 47.33 % of TC under sunlight exposure in winter (cloudy days). The degradation parameters for TC by 10%BiOI/g-C3N4 were optimized using Response surface methods, establishing the optimal conditions for TC degradation (pollutant concentration of 10.94 mg/L, catalyst dosage of 31.34 mg, pH of 4.02), resulting in a degradation efficiency of 95.63 % for TC under the specified conditions. Employing HPLC-MS/MS and 3D EEM techniques, the degradation of TC primarily occurs due to the cleavage of its CC double bonds and CN bonds triggered by free radical attacks, and small molecular acids are produced during the degradation process. The impacts of TC solution treatment on plants were investigated, and the oxidative stress indicators MDA, SOD, POD, and CAT were assessed. The results demonstrated a decrease in all four indicators in plants cultured in TC degradation product solution, further affirming the applicability of 10%BiOI/g-C3N4 in practical scenarios.

Monosymmetric Fe-N4 sites enabling durable proton exchange membrane fuel cell cathode by chemical vapor modification.

The limited durability of metal-nitrogen-carbon electrocatalysts severely restricts their applicability for the oxygen reduction reaction in proton exchange membrane fuel cells. In this study, we employ the chemical vapor modification method to alter the configuration of active sites from FeN4 to the stable monosymmetric FeN2+N'2, along with enhancing the degree of graphitization in the carbon substrate. This improvement effectively addresses the challenges associated with Fe active center leaching caused by N-group protonation and free radicals attack due to the 2-electron oxygen reduction reaction. The electrocatalyst with neoteric active site exhibited excellent durability. During accelerated aging test, the electrocatalyst exhibited negligible decline in its half-wave potential even after undergoing 200,000 potential cycles. Furthermore, when subjected to operational conditions representative of fuel cell systems, the electrocatalyst displayed remarkable durability, sustaining stable performance for a duration exceeding 248 h. The significant improvement in durability provides highly valuable insights for the practical application of metal-nitrogen-carbon electrocatalysts.

Novel ultra-low NOx coal combustion technologies based on local microenvironment targeted regulation. Part 1. Selective oxygenation

Developing a novel high-efficiency coal combustion technology with ultra-low NOx emission is urgently needed to sustain the good ecological environment. Here, the targeted regulation of local microenvironment around fuel-N, such as functional groups, radicals, molecular configurations, and reaction atmosphere, is realized by the selective oxidation. The molecular configurations, including pore networks and microcrystalline structure in coal, are well characterized through synchrotron radiation-induced SAXS (small angle X-ray scattering) and WAXS (wide angle X-ray scattering) simultaneously. Furthermore, by combining density functional theory (DFT) and experiments, the effects of the local microenvironment on the nitrogen transformation and NO evolution during the thermal conversion are focused on. The results indicate that for the PPA oxidation, the H radicals attack the adjacent carbon to pyrrole/pyridine nitrogen, promoting the conversion of fuel-N to HCN. On the other hand, for the H2O2 oxidation, disrupting the π bond electron cloud by the CO and C = O on the ortho carbon of pyrrole/pyridine dominates the NH3 generation. Additionally, the increased La (average graphene layer extent), a3 (average interlayer spacing), σ3 (standard deviation of interlayer spacing) and σ1 (standard deviation of the first-neighbor distribution) induce massive smaller pores, promoting the generation of abundant reaction defects inside the particles. Importantly, the intensified adsorption on abundant active sites lead to the decreased HCN and increased NH3 evolution, which is adverse for the interaction between homogeneous and heterogeneous NO reduction. Interestingly, the PAA selective oxidation can reduce NO emission by 31.72 % - 34.30 % during the air combustion, which is far better than the H2O2 oxidation. Overall, the attack of free radicals on nitrogen-containing heterocycles promotes the conversion of fuel-N to HCN, the adsorption of which on char surfaces can further enhance the heterogeneous reduction in a lean oxygen atmosphere. The work here provides a novel route for developing high-efficiency and low-NOx combustion technologies.

Detection and quantification of 4-oxo-2-nonenal in plant-based meat and beef

Oxidative degradation of lipids and proteins in food causes loss of nutrition, produces genotoxic oxidative byproducts, and increases health concerns. 4-Oxo-2-nonenal (4-ONE) is a highly reactive and toxic aldehyde, recently identified as a novel lipid peroxidation byproduct. However, naturally formed 4-ONE and its interaction with proteins in food are still not fully understood. In this study, methods for the detection and quantification of 4-ONE were further developed and used. The developed method successfully detected the formed lipid oxidation products (LOPs) and protein oxidation products (POPs) during cooking, as well as after in-vitro digestion of plant-based (PB) meat and beef. The method used exhibited consistencies of detection of 4-ONE in raw, cooked, and in-vitro digested PB meat and beef samples. Furthermore, the findings of this study show that PB meat had significantly higher levels of POPs but lower levels of aldehydes (4-ONE and malondialdehyde) than beef samples. The results revealed the LC–MS/MS method for detecting and quantifying 4-ONE as a novel lipid oxidation marker was promising. Furthermore, the results indicated that the protein in PB meat may be prone to covalent modification of aldehyde and free radical attacks, thus reducing its proteolysis during digestion. Future studies should further assess the covalent binding ability of aldehydes (especially 4-ONE) in different types of protein, as well as the interaction between lipid and protein oxidation. Processors should develop new strategies to avoid undesirable LOPs and POPs in PB meat and beef, to improve their nutrition and relieve long-term health concerns.

The construction of Z-scheme heterojunction ZnIn2S4@CuO with enhanced charge transfer capability and its mechanism study for the visible light degradation of tetracycline

In this study, copper oxide (CuO) was prepared by the microwave-assisted hydrothermal technique subsequently, CuO was grown in situ onto different rare metal compounds to prepare Z-scheme heterojunctions to improve the degradation efficiency of tetracycline (TC) in water environments. Various characterization proved the successful synthesis of all composite materials, and the formation of tight heterojunction interfaces, among which, the core–shell structure ZnIn2S4@CuO exhibited excellent photocatalytic degradation capability. Research results indicated that the degradation efficiency of ZnIn2S4@CuO for TC (50 mg/L) in the water environment reached 95.8 %, and the degradation rate is 2.41 times and 12.93 times that of CuO and ZnIn2S4 alone, respectively, the reason is because of the introduction of ZnIn2S4, Z-scheme heterojunction structures and internal electric field (IEF) is constructed and formed to extend the visible light response range of photocatalysts to improve electron-hole separation efficiency, and enhance charge transfer. In addition, ZnIn2S4@CuO-2 exhibited good stability and reproducibility, with no significant loss of activity after five cycles. Finally, the precise locations of free radical attack on TC were investigated by the combined use of high-resolution mass spectrometry (HR-MC) and frontier electron densities (FEDs), and a reasonable degradation pathway was provided. The results of this research provide a new and viable approach to overcome the limitations of conventional photocatalytic materials in terms of limited visible light absorption range and fast carrier recombination rates, which offers promising prospects for a wide range of applications in the field of wastewater purification.

Activation of calcium sulfite by bismuth cobalt-copper perovskite-manganese dioxide composite for efficient degradation of metronidazole

The highly efficient BiCo0.5Cu0.5O3-MnO2 catalyst was prepared using the hydrothermal method and utilized for the first time to activate sulfite for degrading metronidazole (MNZ) in this study. Physicochemical analysis of the BiCo0.5Cu0.5O3-MnO2 catalyst was performed using XRD, FTIR, BET, SEM, TEM, and XPS, confirming the successful synthesis of catalyst. BiCo0.5Cu0.5O3-MnO2 demonstrated a larger specific surface area, a more uniform pore structure, and prevented perovskite agglomeration. The catalyst effectively activated CaSO3, resulting in the degradation of 99.94 % of MNZ within 30 min, showing excellent catalytic performance. Quenching experiments and EPR tests indicated that SO•-4, SO•-5 and 1O2 were the main reactive species, with the oxygen vacancy on the catalyst surface playing a crucial role in accelerating the formation of reactive species and electron transfer. Moreover, the valence transformation of Co, Cu, and Mn was identified as the main contributor to the activation of CaSO3, demonstrating significant synergistic effects. Liquid chromatography-mass spectrometry detected eleven intermediates, revealing that the BiCo0.5Cu0.5O3-MnO2/CaSO3 system could convert MNZ into low-toxicity products through three potential degradation pathways. Density functional theory (DFT) calculations showed that higher Fukui indices of MNZ sites were more susceptible to free radical attack. The BiCo0.5Cu0.5O3-MnO2/CaSO3 system also exhibited excellent degradability to different natural water bodies and other pollutants. Furthermore, the catalyst displayed strong stability and outstanding catalytic performance after 5 cycles. This study presents a versatile strategy for developing highly efficient green catalysts, which could be utilized in organic wastewater treatment.

Investigation of the Structure of the Complex Oligomeric Mixture Formed During Grignard Tetramethylation of N-benzylphthalimide

TMIO or 1,1,3,3-tetramethylisoindolin-2-yloxyl (5, Scheme 1) is one of the most versatile isoindoline nitroxides due to its applications [1, 2] and a variety of important advantages such as thermal stability, low reactivity towards olefins [3], symmetrical nature [4], UV detectability [5] and relative inertness to free radical attack [4][4]. The most common and effective pathway for synthesizing 5 remains the Grignard-based approach in which N-benzylphthalimide 1 is treated with methylmagnesium halide in refluxing toluene, followed by subsequent debenzylation and oxidation of the resulting secondary amine

Pelatihan Pengolahan Wortel Menjadi Stick Sehat Pengontrol Kadar Glukosa Darah Bagi Ibu PKK di Desa Temulus Mejobo Kudus

Carrots are a type of tuber vegetable that is rich in antioxidant compounds, including vitamin C and beta carotene. One of the functions of antioxidants is to protect pancreatic beta cells from free radical attacks and is also a vasodilator in preventing cardiovascular disorders Damage to pancreatic beta cells can result in high blood glucose levels. Carrots have a taste are not pleasant to consume, so they are made in stick form, which is a snack that is easy to consume every day with a delicious taste and is effective in controlling blood glucose levels. The aim of this activity is to increase the knowledge, skills of PKK’s mother in Temulus about the benefits of carrots and how to process them into healthy sticks so they are delicious to consume. The methods used are descriptive, explanation, discussion and practice. The result of this activity was an increase in knowledge from the good category of 10% (3 people) to 46.67% (14 people) with a total of 30 participants. The conclusion of this activity is the increasing knowledge of PKK mothers in Temulus about the benefits of carrots as controlling blood glucose levels and increasing the skills of PKK mothers in Temulas in processing carrots into healthy sticks to control blood glucose levels.

The promoting and inhibitory mechanism of interaction between waste tires and Spirulina on their co-pyrolysis

Energy utilization of biomass and waste is an important thrust for carbon emission reduction. Co-pyrolysis is conductive to efficiently converting algae and waste tires, due to their complementary pyrolysis characteristics. However, the influence of the interaction between algae and waste tires on co-pyrolysis behavior is still controversial, due to the internal mechanism of interaction is unclear. Therefore, in this study, mechanism experiments and theoretical calculations were used to comprehensively investigate the interaction mechanism between Spirulina (SP) and waste tires (WT). The co-pyrolysis of SP and WT can be divided into two main steps: low-temperature SP decomposition and high-temperature WT decomposition. The activation energies of WT and mixture increase with the conversion rate, while those of SP change little at low conversion rates (<60 %). The pyrolysis activation energies of mixture are lower than the theoretical values, as the blending ratio of SP below 50 %. The interaction between SP and WT has both promoting and inhibiting effects on the pyrolysis of mixture. The attack of free radicals from SP pyrolysis and ash in WT promotes the pyrolysis of mixture, but the low-temperature polymerization reactions and high-temperature aromatization reactions inhibit the release of pyrolysis products. The formation of benzene compound is promoted due to the attack of free radicals and the polymerization between SP and WT.

Advanced oxidation process/coagulation coupled with membrane distillation (AOP/Coag-MD) for efficient ammonia recovery: Elucidating biofouling control performance and mechanism

The inadequate understanding of the biofouling formation mechanism and the absence of effective control have inhibited the commercial application of membrane distillation (MD). In this study, an advanced oxidation process (AOP)/coagulation-coupled (Coag) membrane distillation system was proposed and exhibited the potential for MD ammonia recovery (recovery rate: 94.1%). Extracellular polymeric substances (EPS) and soluble microbial products (SMP) components such as humic acid and tryptophan-like proteins were disrupted and degraded in the digestate. The curtailment and sterilizing efficiency of AOP on biofilm growth was also verified by optical coherence tomography (OCT) in situ real-time monitoring and confocal laser scanning microscopy (CLSM). Peroxymonosulfate (PMS) was activated to generate sulfate (SO4•-) and hydroxyl radicals (HO•), which altered the microbial community. After oxidative treatment, 16 S rRNA sequencing indicated that the dominant phylum of the microbial community evolved into Firmicutes. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis demonstrated that free radicals produced by PMS could disrupt cells' signaling molecules and interactions. In conjunction with these analyses, the mechanisms of response to free radical attack by Gram-negative bacteria, Gram-positive bacteria, and fungi were revealed. This research provided new insights into the field of membrane fouling control for membrane technology resource recovery processes, broadening the impact of AOP applications on microbiological response and fate in the environment.

Biocompatible citrate-cysteine complexes of manganese as effective antioxidants: Experimental and computational studies

Many clinical studies have evaluated the ability of sulfur-containing antioxidants to prevent oxidative stress, a major cause of cancer, Parkinson's, and Alzheimer's disease. Cysteine complexes of manganese modified with citric acid were synthesized by a one-pot procedure in two molar ratios and at two different temperatures (90°C, 140°C). The synthesized complexes were studied using FT-IR, UV-Vis, NMR, and EDX. At the lower temperature, a hydrogel was formed, and a thiazolopyridine ring was formed at a temperature of 140°C which was complexed with manganese. Infrared and electronic absorption spectroscopy confirmed that manganese binding occurred via the oxygen atoms of COO. The complexes also exhibited strong fluorescence with excitation/emission peak wavelengths of 350/418 nm. The synthesized compounds showed efficient activity for superoxide scavenging (> 70%), which was evaluated by a pyrogallol autoxidation method. MTT assay studies confirmed the noncytotoxic nature of all the prepared samples. The Gaussian 09 program was used to optimize the structural configurations of the ligands and complexes based on DFT by the B3LYP/6-31+G(d) basis set. To evaluate the softness of both the ligand and the complex, an investigation of the HOMO-LUMO gaps was carried out. In addition, UV-vis spectra of Mn complexes obtained from the time-dependent DFT calculations show a strong peak in the range of 380-390 nm, which is in good agreement with our experimental findings. The results revealed that the oxygen atoms of citrate and cysteine are the most potential sites to interact with the Mn atom. Besides, the calculated average local ionization energies showed that the Mn atom is the most energetically favored and vulnerable site to an electrophilic or free radical attack.