Organic Compounds Research Articles

Towards the mechanical stability of biocrusts in drylands: Insights from inorganic ions and organic compounds and their interactions

Biocrusts are an important component of dryland ecosystems as they perform crucial ecological functions like stabilizing soils, mediating the hydrological cycle, and improving nutrient availability. The high mechanical stability of biocrusts is understood to be linked to exopolymeric substances (EPS), which in turn, are responsible for the adsorption of various ions and chemical compounds. This study aimed to investigate the chemical composition of biocrusts and assess potential correlations between their chemical composition and mechanical stability. Samples of three types of biocrusts (cyanobacteria, cyanobacteria and moss mixed, and moss crusts) and bare soil (as control) were collected from the northern Loess Plateau of China. The inorganic ions and organic compounds present in biocrusts were quantified using inductively coupled plasma-optic emission spectrometry, ion chromatography, and gas chromatography-mass spectrometry. Biocrust mechanical stability was assessed by penetration resistance (PR) and the mean weight diameter (MWD) of aggregates. Finally, the contribution of inorganic ions and organic compounds to the stability of the biocrusts was elucidated. The results indicated that all three types of biocrusts were more stable than bare soil, with moss crusts being the most stable. Chemical analyses revealed an enrichment of inorganic ions such as K+, Ca2+, Na+, Mg2+, SO42–, and halogen ions within the biocrusts, while they showed a depletion of Fe2+, Al3+, and NO3–. Ten types of organic compounds were identified in biocrusts and bare soil, with medium-chain alkanes and long-chain acids being the dominant compounds. In some cases, acids accounted for more than 40 % of the total organic compound content of the biocrusts. Redundancy analysis showed that the content of inorganic ions, such as Ca2+ and Mg2+, and organic compounds such as acids, amides, and alkenes, exhibited the closest association with the biocrust stability. Partial least squares path modeling indicated that both inorganic ions and organic compounds indirectly affected biocrust stability by influencing electric conductivity, bulk density, EPS, and fine particle (clay and silt) content. A strong association was found between the inorganic ions and PR or MWD (0.658 and 0.744, respectively), whilst the total effect of organic compounds on PR and MWD was 0.814 and 0.801, respectively. It is suggested that both the magnitude and types of chemicals associated with EPS indicate their capability to grant mechanical stability of the biocrusts, which in turn is conducive to maintaining the critical functions of biocrusts in global drylands.

Study on pyrolysis process and mechanism of organic coating of waste polyesterimide enameled wire based on density functional theory

The pyrolysis treatment of waste polyesterimide enameled wire offers significant advantages such as continuous processing, non-hazardous nature, and high resource recovery rate. However, research on its pyrolysis process and mechanism remains insufficiently explored. In this study, techniques including thermogravimetry (TG), Fourier transform infrared spectroscopy(FT-IR), pyrolysis–gas chromatography-mass spectrometry(Py-GC/MS) were employed to investigate pyrolysis temperature, weight loss rate, pyrolysis and kinetic parameters, composition and distribution of pyrolysis products, and changes in functional groups under different temperatures and heating rates. The pyrolysis of polyesterimide enameled wire can be divided into three stages: volatilization of specific components (314.8 °C,1.6 %), rapid decomposition of polyesterimide (435.2 °C, 44.7 %), and generation of small organic molecules with the fixation of pyrolytic carbon (750 °C, 9.0 %). The main components of the pyrolysis gas products include aromatic compounds, ethers, aromatics, ketones, and carbon dioxide. At 400 °C, a substantial amount of pyrolysis gas products and free radicals are produced, with an increase in aromatic hydrocarbons. The carbon distribution in the pyrolysis products mainly focuses on C6-C10 and C11-C15, and many organic compounds such as benzoic acid, phenol, and aniline are generated. Based on density functional theory, the bond dissociation energies in the polyesterimide were calculated. This clarified the possible thermal decomposition pathways of the polyesterimide and provided the energy barrier values, elucidating the generation mechanism of pyrolysis products during thermal decomposition. The copper atom in specific location reduces the negative ESP of O and increases the positive ESP of H in EPI, which makes H more likely to attach to O. The presence of Cu increases the ESP range and promote the pyrolysis process. This study provides a theoretical basis for the high-value recycling of waste polyesterimide enamelled wire.

Molecular insights into the degradation of organic matter from secondary swine wastewater effluent: A comparative study of advanced oxidation processes

Advanced oxidation processes (AOPs) are promising for the treatment of secondary swine wastewater effluents, however, the molecular-level understanding of effluent organic matter (EfOM) removal and transformation during AOPs is limited. This study employed molecular-level characterization based on Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) and bulk characterizations to investigate these processes in various AOPs, including Cu-Fenton, UV-Cu-Fenton, Fenton, UV-Fenton, and UV/H2O2 treatments. Our findings revealed that the removal rates of dissolved organic carbon and EfOM molecules follow the sequence of UV-Fenton > Fenton > UV-Cu-Fenton > UV/H2O2 > Cu-Fenton, correlating with the rates of H2O2 decomposition during reactions. AOPs with faster H2O2 decomposition, indicative of higher reactive oxygen species generation, predominantly mineralize rather than transform EfOM. Linkage analysis highlighted oxygen addition and deamination as the primary transformation reactions, with variations in the dominance levels of these reactions across different AOPs. Recalcitrant molecule, particularly CHNO and CHO types, including low-molecular-weight carboxyl-rich alicyclic molecules, pose challenges in treatment. To enhance the efficacy of secondary effluent treatment, strategies focusing on the targeted removal of such recalcitrant EfOM should be developed. This study provided new insights into the selection and optimization of AOPs for secondary swine wastewater effluent treatment.

A highly water-soluble phenoxazine quaternary ammonium compound catholyte for pH-neutral aqueous organic redox flow batteries

The pH-neutral aqueous redox flow battery (ARFB) is one of the most attractive flow batteries due to its non-corrosiveness, low-cost, and wider electrochemical stability window compared to those with acidic or alkaline electrolytes. However, there are few families of organic redox-active molecules available as catholyte materials for pH-neutral ARFBs. Herein, through incorporation of quaternary ammonium moiety into the redox-active phenoxazine nucleus, an organic catholyte material, N, N, N-trimethyl-2-(10H-phenoxazin-10-yl) ethan-1-aminium chloride (NEt-POZ) is achieved for pH-neutral ARFBs. The NEt-POZ has a high redox potential of 0.79 V versus SHE and rapid redox kinetics (0.23 cm s−1) as well as high water-solubility (∼2.6 M in H2O). Paired with a methyl viologen (MV) anolyte in the pH-neutral aqueous electrolyte, a viologen-phenoxazine ARFB full cell is assembled, which shows an open circuit voltage of ∼1.23 V. However, the results of long-term cycling experiments indicate low Coulomb efficiency and rapid declining capacity of the NEt-POZ catholyte. The mechanism analysis unveils that the unstable doubly oxidized tri-cations (NEt-POZ3+) formed via the disproportionation of radical di-cations (NEt-POZ2+) in solution readily react with chloride anions to form poly-chlorinated derivatives, which precipitate from the catholyte due to their poor water solubility, leading to a rapid decrease in capacity. When there is no chloride present in the electrolyte solution, highly reactive NEt-POZ3+ cations can interact with other counter-anions (such as sulfate and carbonate ions) and even water to form complex adducts.

Peat-based amendment of soils reduces the complexity of the volatile profile in cultivated black truffles.

Truffle cultivation is evolving rapidly and new agronomic practices such as 'truffle nests' (localized peat amendments of the orchard soil) are being developed. Truffle nests improve the shape of truffles and their depth in the soil and reduce the occurrence of insect damage but have also raised concerns about their impact on the ripeness and maturity of the harvested truffles. In this study, the effect of the nests on the volatile organic compounds profile and the aromatic profile of black truffles was evaluated, as well as the existence of perceptible sensorial differences in truffles. For this, truffles growing in nests were compared with truffles growing in the bulk soil of the same host tree. Gas chromatography showed that nest truffles had a less complex volatile organic compound profile than bulk-soil truffles. Olfactometry indicated that nest truffles were associated with higher modified frequency values of odorants corresponding to sulfur-containing compounds. Despite this, sensory evaluation with consumers could not clearly show that nest truffles can be distinguished sensorially from bulk-soil truffles. The results prove that soil conditions can influence the aromatic profile of truffles and thus suggest the possibility of managing truffle aroma using agronomic practices. © 2024 The Author(s). Journal of The Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Volatilome: A Novel Tool for Risk Scoring in Ischemic Heart Disease.

Developing a novel risk score for accurate assessment of cardiovascular disease (CVD) morbidity and mortality is an urgent need in terms of early prevention and diagnosis and, thereafter, management, particularly of ischemic heart disease. The currently used scores for the evaluation of cardiovascular disease based on the classical risk factors suffer from severe limitations, including inaccurate predictive values. Therefore, we suggest adding a novel non-classical risk factor, including the level of specific exhaled volatile organic compounds that are associated with ischemic heart disease, to the SCORE2 and SCORE2-OP algorithms. Adding these nonclassical risk factors can be used together with the classical risk factors (gender, smoking, total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, diabetes mellitus, arterial hypertension, ethnicity, etc.) to develop a new algorithm and further program to be used widely.

Modulating fine flavor cocoa attributes: Impact of seed-to-bean transformation under controlled conditions on metabolite, volatile and sensory profiles

Fine-flavored chocolates are distinguished by their complex and distinct flavor profiles, which includes notes such as floral, fruity, nutty, and spicy. This study sought to modulate the flavor development of chocolates by establishing controlled processing conditions during the transformation from seed to bean in a laboratory setting, to produce superior quality chocolates. Our experimental setup comprised two varying temperature levels (30 °C and 45 °C) and three organic acids (OAs: acetic, lactic, and citric acids) at concentrations of 1–30 g/L to adjust the pH of the transformation system. Our study focused on how these conditions affect the development of distinct flavor profiles in chocolate bars, emphasizing the enhancement of fine-flavor notes. Flavor development was monitored through the untargeted metabolomics of cocoa beans and analyzing the volatile compounds and sensory profiles of the resultant chocolates. This study revealed that OA concentration markedly influenced metabolite formation, particularly affecting peptides, volatile organic compounds, and flavor notes. Chocolates derived from seeds processed with 30 g/L acid solutions demonstrated enhanced fruitiness and acidity, whereas those processed with 1 g/L acid solutions exhibited pronounced nuttiness and cocoa taste attributes but lower acidity. These findings underscore the significance of meticulously managing flavor development processes to produce fine-flavored chocolates with unique aromatic profiles. Crucially, variables in the controlling process, such as temperature and pH, are essential for fine-tuning flavor attributes, enabling the correlation and identification of key quality biomarkers to elucidate flavor development pathways.

Volatilome is Inflammasome- and Lipidome-dependent in Ischemic Heart Disease.

Ischemic heart disease (IHD) is a pathology of global interest because it is widespread and has high morbidity and mortality. IHD pathophysiology involves local and systemic changes, including lipidomic, proteomic, and inflammasome changes in serum plasma. The modulation in these metabolites is viable in the pre-IHD, during the IHD period, and after management of IHD in all forms, including lifestyle changes and pharmacological and surgical interventions. Therefore, these biochemical markers (metabolite changes; lipidome, inflammasome, proteome) can be used for early prevention, treatment strategy, assessment of the patient's response to the treatment, diagnosis, and determination of prognosis. Lipidomic changes are associated with the severity of inflammation and disorder in the lipidome component, and correlation is related to disturbance of inflammasome components. Main inflammasome biomarkers that are associated with coronary artery disease progression include IL-1β, Nucleotide-binding oligomerization domain- like receptor family pyrin domain containing 3 (NLRP3), and caspase-1. Meanwhile, the main lipidome biomarkers related to coronary artery disease development involve plasmalogen lipids, lysophosphatidylethanolamine (LPE), and phosphatidylethanolamine (PE). The hypothesis of this paper is that the changes in the volatile organic compounds associated with inflammasome and lipidome changes in patients with coronary artery disease are various and depend on the severity and risk factor for death from cardiovascular disease in the time span of 10 years. In this paper, we explore the potential origin and pathway in which the lipidome and or inflammasome molecules could be excreted in the exhaled air in the form of volatile organic compounds (VOCs).

Modification and mechanistic study of fluid/fluid and carbonate rock/fluid interfaces using a glycolipid biosurfactant from an indigenous strain of Gordonia terrae for MEOR applications

To clarify the mechanism of the interface behavior between carbonate surface/biosurfactant solution/oil systems, the interfacial tension (IFT), surface wettability, spreading coefficient (SC), and capillary number were investigated with regard to the synergistic effects of a biosurfactant from an indigenous Gordonia terrae strain (isolated from an Iranian oil reservoir), formation water salinity, and pH using response surface methodology (RSM-CCD). According to the analysis of variance results, the process effectively depicted by the quadratic model demonstrated statistical significance in terms of the responses of IFT, wettability alteration, and SC, which were significantly affected by biosurfactant concentration. The optimal conditions were 0.260 g/L biosurfactant, 36.202 g/L salinity, and a pH of 5.9. Accordingly, the quadratic model was verified using the estimated optimal parameters, thereby confirming the accuracy of the model in which a strongly water-wet surface (contact angle change from 159° to 31°) and IFT reduction (from 23.96 to 1.26 mN/m) resulted in an SC of near-zero value (−0.18) and 25 % recovery of oil during the imbibition experiments after secondary water flooding. The desorption of the polar components of crude oil from the dolomite rock surface was also investigated through determining the un-coverage ratios of the elements using energy dispersive X-ray microanalysis and characterization. Although the solutions containing biosurfactants contributed to the alteration of the rock surface wettability, their performance strongly depended on the pH and salinity, resulting in different desorption ratios. The desorption of approximately 40 % of the adsorbed organic compounds from the carbonate surface was a critical limiting factor affecting the surface properties of the rock, and was responsible for altering the wettability to water-wet conditions. The results of this study are expected to contribute to the development of effective biosurfactant-flooding techniques for MEOR.

Hydroxylated SiO2-modified {0 0 1}-TiO2 nanosheets as a surface multifunctional photocatalyst for enhanced degradation of gaseous toluene

The relatively weak activity and serious deactivation of anatase TiO2 nanosheet catalysts with highly exposed {001} facets ({001}-TiO2) limits its wide application in photocatalytic degradation of gaseous pollutants. Herein, we propose a hybrid photocatalyst composed of {001}-TiO2 and SiO2 with numerous hydroxyl groups (denoted as {001}-TiO2/HO-SiO2). The catalyst showed excellent performance for gaseous toluene degradation under UV illumination, with 99.2 % removal efficiency and 204.7 μmol L−1 CO2 yield (about 85.9 % mineralization efficiency) within 120 min. It also demonstrated superior durability over five consecutive cycles of toluene photodegradation. The modification of HO–SiO2 on {001}-TiO2 facilitate the selective adsorption of toluene on the catalyst surface by H-bonding interaction, and make the major poisoning species, benzoic acid, easily desorb from the surface, reducing the catalyst inactivation. Most importantly, we found that the formed TiOSi bond promotes the separation of photogenerated electron–hole pairs, and provides abundant available electrons for the formation of reactive oxygen radicals and the left holes for the conversion of toluene to benzyl radicals or oxidation of H2O to hydroxyl radicals, which results in the improved activity. This study highlights the importance of the introduction of secondary components with special functions on TiO2, which is helpful for the design of photocatalysts with high performance and anti-deactivation ability for treatment of volatile organic compounds.

Introduction of mesopores effectively enhances the accessibility of volatile organic compounds within the micropores of covalent triazine frameworks

Porous organic polymers (POPs) with abundant pores have great potential for the treatment of volatile organic compounds (VOCs). However, narrow micropores increase gas diffusion resistance and limit the accessibility of VOCs within the micropores. Here, we have synthesized microporous covalent triazine frameworks (mpCTFs) with abundant mesopores using nano-silica. And the effects of the introduced mesopore structure on the sorption performances of CTF were further investigated by 1,2-dichloroethane adsorption. The results indicate that mpCTF12.5 has the most suitable mesopore volume, and its specific surface area and total pore volume are 2.40 and 2.17 times that of CTF, respectively. Meanwhile, the mpCTF12.5 exhibited excellent adsorption performance for methanol, ethanol, acetone, benzene, ethyl acetate, 1,2-dichloroethane and toluene due to the multiple C-H…O, C-H…Cl, O-H…N and C-H…π interactions between VOCs and mpCTFX framework, demonstrated via DFT calculations. Additionally, the two-component gas-competitive adsorption behavior and the impact of water vapor on the adsorption performance of mpCTFX were investigated, with the adsorption mechanism thoroughly analyzed using the GCMC model. The introduction of abundant mesopores undoubtedly shortened the diffusion paths within the micropores of CTFs, significantly enhancing their accessibility for VOC adsorption. This study presents a viable strategy to improve the performance of porous materials in VOC adsorption applications.

The source of volatile organic compounds pollution and its effect on ozone in high-altitude areas

Volatile organic compounds (VOCs) are crucial precursors in the formation of ozone (O3). The sources of pollution are complex and significantly impact O3 generation. Long-term exposure to high-concentration O3 environments causes serious damage to organisms. High-altitude areas experience continuous high temperatures and strong solar radiation, which can easily produce O3 through photochemical reactions, making these areas prone to frequent air pollution. This study utilizes the National Positioning Station of the Yinchuan Urban Ecosystem in Ningxia to conduct field synchronous observations, gathering data on VOCs, meteorological variables, and O3. By employing machine learning algorithms, we examined the seasonal distribution characteristics of VOCs, their pollution sources, and their impact on O3. The results show that the seasonal distribution of VOCs areas is low in spring and autumn and high in summer and winter. The components with higher volume fraction contribution are m-tolualdehyde in spring and summer, ethane in autumn, and acetylene in winter. The main emission sources of VOCs pollution are hydrocarbon volatile emission in spring and winter, solvent volatilization emission in summer, and industrial sources in autumn. VOCs have a negative effect on O3, with a greater impact in winter and spring, evidenced by standardized effect values of −0.26 and −0.24. The key components affecting O3 in VOCs vary by season. Aromatic hydrocarbons are the key components in spring and winter, with contribution rates of 22 % and 21.3 %. Alkenes are the key components in summer and autumn (24.5 % and 26.8 %). Among meteorological variables, temperature is the key factor affecting O3, while wind speed is the key factor affecting O3 only in winter. This study aims to clarify the sources of VOCs pollution in different seasons and their impact on O3, providing a theoretical basis and technical support for the prevention and control of VOCs and O3 pollution in high-altitude areas.

Ionic Liquid-Based Green Solvents for Extraction and Purification of Natural Plant Products

Introduction: This research paper explores the environmental sustainability of ionic liquid-based green solvents in the extraction and purification of natural plant products, with a focus on their entire life cycle. The objectives of the study were to assess the environmental impact of ionic liquid synthesis, energy consumption, water usage, emissions, recycling rates, policy effects, and stakeholder perceptions. Methods: Methodologically, we conducted a comprehensive Life Cycle Assessment (LCA) that involved primary data collection through field surveys and interviews with key stakeholders in the ionic liquid production and usage industry across various regions in India. The data were analyzed using specialized LCA software tools to quantify environmental impacts. Key findings include the identification of synthesis as a major contributor to environmental impact, emphasizing the need for greener synthesis methods. Results: The study revealed the significant carbon footprint, energy consumption, and water usage during production, highlighting opportunities for improvement. Emissions data underscored the importance of emission control measures, particularly for greenhouse gases and volatile organic compounds. Recycling and reuse were identified as environmentally friendly disposal methods. Policy compliance varied among stakeholders, indicating room for stricter regulations. Stakeholder perceptions varied, with researchers having the most positive outlook. Implications of the findings extend to sustainable chemistry practices, emphasizing interdisciplinary collaboration and the importance of considering the entire life cycle of chemical processes. Conclusion: This research contributes to a deeper understanding of green solvents and provides a foundation for promoting sustainable practices in industrial processes in India and globally.

1,3,4-Oxadiazole Scaffold in Antidiabetic Drug Discovery: An Overview.

Diabetes mellitus is one of the biggest challenges for the scientific community in the 21st century. With the increasing number of cases of diabetes and drug-resistant diabetes, there is an urgent need to develop new potent molecules capable of combating this cruel disease. Medicinal chemistry concerns the discovery, development, identification, and interpretation of the mode of action of biologically active compounds at the molecular level. Oxadiazole-based derivatives have come up as a potential option for antidiabetic drug research. Oxadiazole is a five-membered heterocyclic organic compound containing two nitrogen atoms and one oxygen atom in its ring. Oxadiazole hybrids have shown the ability to improve glucose tolerance, enhance insulin sensitivity, and reduce fasting blood glucose levels. The mechanisms underlying the antidiabetic effects of oxadiazole involve the modulation of molecular targets such as peroxisome proliferator-activated receptor gamma (PPARγ), α-glucosidase, α-amylase and GSK-3β which regulate glucose metabolism and insulin secretion. The present review article describes the chemical structure and properties of oxadiazoles and highlights the antidiabetic activity through action on different targets. The SAR for the oxadiazole hybrids has been discussed in this article, which will pave the way for the design and development of new 1,3,4-oxadiazole derivatives as promising antidiabetic agents in the future. We expect that this article will provide comprehensive knowledge and current innovation on oxadiazole derivatives with antidiabetic potential and will fulfil the needs of the scientific community in designing and developing efficacious antidiabetic agents.

Mechanistic effects of graphitization and oxygen functional groups on benzene competitive adsorption of porous carbon under high humidity conditions

Porous carbon is an ideal adsorbent for the elimination of volatile organic compounds (VOCs) attributed to their price, availability and excellent adsorption capacity. However, there are significant variation in the adsorption capacity and adsorption selectivity of different precursors for VOCs under humid conditions after modification because of the differences in their own structural properties. In this study, graphitized hydrophobic porous carbon with excellent specific surface area was successfully synthesized by selecting bamboo fiber, maize, coconut husk and coal as precursors and potassium hydroxide as an activator. Among them, the dynamic adsorption capacity of benzene in the sample with bamboo fiber as precursor was maintained at 74.7% under the high humidity condition (RH90%) compared with the dry state (RH0%). Grand Canonical Monte Carlo (GCMC) simulations and weak interaction force analyses showed that enhanced dispersion attraction between graphitized carbon surfaces and benzene molecules in comparison to disordered carbon surfaces. The existence of oxygen functional groups enhanced the interaction between porous carbon and water through hydrogen bonding leading to preferential adsorption of water molecules, which resulting in the decrease of their adsorption performance in wet condition. This research provided theoretical and experimental views of the effects of graphitization and oxygen functional groups on the competitive adsorption capture of benzene and water by porous carbon, which further provided a reliable approach to synthesizing porous carbon with high adsorption capture for benzene removal in high humidity environments.

Vocs pollution and respiratory exposure in commercial and residential underground parking garages

The indoor air quality in Underground Parking Garages (UPGs) has deteriorated significantly, primarily due to the high concentrations of particulate matter and volatile organic compounds (VOCs) emitted by idling or low-speed motor vehicles. However, the compositional characteristics and respiratory exposure to VOCs in UPGs have not been quantitatively analyzed. To establish a method for investigating the respiratory exposure to VOCs among different populations in UPGs, a three-dimensional dynamic diffusion model of indoor pollutants was developed based on monitoring data from 116 components in various UPGs in a large city in northern China. The results indicated that air pollution in underground spaces poses significant health risks to workers and children. Furthermore, a comprehensive approach is essential for improving ventilation capacity and air quality in underground transportation spaces.

Polymerization of redox-active alizarin in biomass porous carbon with enhanced cycling stability for supercapacitor

Redox-active organic molecules have optimistic application prospects in energy storage due to their high theoretical capacitance, designable electrochemical activity and environmental friendliness. However, low conductivity and solubility in electrolyte severely hinder their redox activity. Here, alizarin molecules containing carbonyl and phenolic hydroxyl are encapsulated in biomass-derived porous carbon, and stable alizarin polymers are further grown on porous carbon substrate by electrochemical polymerization. Porous carbon as conductive network can improve electron transport properties, and provide suitable accommodation environment for confinement and polymerization of alizarin. The electrochemical polymerization strategy on carbon substrate allows alizarin to be connected by rigid C-O-C bond, which inhibits the dissolution of organic monomers while maintaining redox activity. The optimized polyalizarin/porous carbon composite (PAZ/PC-0.5) exhibits superior charge storage performance, with a specific capacitance of 355.8 F g−1 at 1 A g−1 and 220.8 F g−1 at high current density of 30 A g−1. Moreover, PAZ/PC electrode has more durable long-term charge-discharge stability (capacitance retention is 98 % after 10,000 charge and discharge cycles). The assembled symmetrical supercapacitor exhibits excellent energy-power characteristics (21.4 Wh kg−1 at 700 W kg−1) and durable cycle stability. This work sheds light on the design of stable organic electrode towards high-performance supercapacitor.

A Brief Review Depending on the Chemistry of Isatin in Single Pot Technique Towards the Construction of Significant and Valuable Heterocyclic Scaffolds

Abstract:: The term isatin and its derivative-based MCRs have emerged over the years as a versatile, environment-friendly, and very promising platform for the construction of highly enabling bioactive organic scaffolds such as drugs, natural products, pharmaceuticals etc. In the world of recent advancements, the one-pot strategy based on isatin has come to the forefront of synthetic chemistry for the activation of small organic molecules. This present survey touched on the chemistry of isatin employed over the past decade to sketch and for the creation of various types of organic molecules consisting of heterocyclic or spiro-heterocyclic skeletons via one-pot methodology.

Nano Filtration Techniques in Waste Water Treatment

Nano filters, based on nanotechnology to improve filtration processes, offer sophisticated solutions for contaminant removal from liquids and gases. The filters in this group include polymeric membranes with a pore size of 1-100 nanometres, ceramic membranes that are tolerant to chemicals, and carbon nanotube and graphene-based filters with advancedpermeability and selectivity. Recently, differentiated nanomaterials have been developed to make composite membranes with improved performance and durability. However, NF have disadvantages such as membrane fouling and high production costs. In this respect, research is currently being done to come up with solutions to the challenges, optimize the integration of nanomaterials, and realize application possibilities in water treatment, air purification, and industrial processes. On the whole, NF stand as the radical improvement filtration technology has so far achieved, and further research is bound to make them more efficient and cheaper About 17–19 million people in the world lack access to clean water. It is estimated that about 3.4 million people die every year from water scarcity, sanitation, and hygiene-related problems out of which 99% of deaths occurin developing countries. In recent years, water contamination has become a global environmental concern. The paper providesinsights into advancements in wastewater treatment through nano-filters. The paper focuses on evaluating the effectiveness ofnanomembranes in removing containments such as inorganic salts, organic compounds, and heavy metals. Additionally, the paper gives information about performance based on a comparison of the tractional filters and RO in terms of flexibility, durability, efficiency, and cost-effectiveness. Furthermore, it explores the application of NF in industries such as textile, pharmaceuticals, and agriculture and evaluates the versatility and effectiveness in these sectors.

Synthesis of Mesoporous ZnO•SiO2 Nanocomposite from Rice Husk for Enhanced Degradation of Organic Substances Including Janus Green B under Visible Light

Rice husk (RH) is often mentioned as an agricultural by-product, often used in the pass as fertilizer and for raw burning. With modern science, RH have been researched and found many new potential benefits and applications. In this study, RH were used to synthesize amorphous SiO2, which was used to prepare the ZnO•SiO2 nanocomposites by a hydrothermal method. The as-synthesized materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and N2 adsorption/desorption isotherm. Their photocatalytic properties were studied by an ultraviolet-vis spectrophotometer and a fluorescence spectrophotometer. The ZnO•SiO2 nanocomposite has an excellent ability to degrade organic substances such as dyes, antibiotics, caffeine, etc. The effects of operating parameters on the photo-degradation reaction progress, including catalyst dosage, initial dye concentration, and pH of the initial dye were investigated in detail. In addition, the photodegradation rate of the dye on the ZnO•SiO2 nanocomposite was evaluated using the pseudo-first-order model. The ZnO•SiO2 nanocomposite can be used as a photocatalyst for wastewater treatment as it detaches much more easily from the solution. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).