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Perfluoroalkyl carboxylic acids (PFCAs) exhibit high chemical and thermal stability, rendering them versatile for various applications. However, their notable toxicity poses environmental and human health concerns. Detecting trace amounts of these chemicals is crucial to mitigate risks. Electrochemical sensors surpass traditional methods in sensitivity, selectivity, and cost-effectiveness. In this study, a graphene nanosheet-based sensor was developed for detecting perfluorooctanoic acid (PFOA) and perfluorodecanoic acid (PFDA). Using the Hummer method, graphene nanosheets were synthesized and characterized in terms of morphology, structural ordering, and surface topology. Ab initio molecular dynamics simulations determined the molecular interaction of per- and poly-fluoroalkyl substances (PFASs) with the sensor material. The sensor exhibited high sensitivity (50.75 µA·µM-1·cm-2 for PFOA and 29.58 µA·µM-1·cm-2 for PFDA) and low detection limits (10.4 nM for PFOA and 16.6 nM for PFDA) within the electrode dynamic linearity range of 0.05-500.0 µM (PFOA) and 0.08-500.0 µM (PFDA). Under optimal conditions, the sensor demonstrated excellent selectivity and recovery in testing for PFOA and PFDA in environmental samples, including spiked soil, water, spoiled vegetables, and fruit samples.
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The growing population and waste biomass accumulation are leading to increased environmental pollution and climate change. Waste biomass comprising of nutrient rich components has promising potential to produce value-added products for sustainable environmental solutions. This review explores the critical role of bio-based heterogeneous catalysts in enabling sustainable waste biomass utilization. In industrial chemical transformations, over 95% involve catalysts, with more than 90% being heterogeneous systems, prized for their robustness, ease of product separation, and reusability. Bio-based heterogeneous catalysts address the pressing need for sustainable waste biomass management, allowing the conversion of diverse waste biomasses into biodiesel as valuable products. Research on these catalysts, particularly for biodiesel production, has shown yields exceeding 90% with enhanced catalyst reusability. This surge in research is evident from the increasing number of published articles, notably in 2022 and 2023, highlighting growing interest and importance in the scientific community. The synthesis of these catalysts is examined, including novel approaches and techniques to enhance their efficiency, selectivity, and stability. The challenges with their feasible solutions of heterogeneous catalysts in catalyst-based processes are addressed. Altogether, this review underscores the immense potential of bio-based heterogeneous catalysts in sustainable waste biomass utilization, aligning with resource efficiency and environmental conservation goals while offering distinct insights and perspectives on the latest innovations in the field.
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One of the common causes of water pollution is the presence of toxic dye-based effluents, which can pose a serious threat to the ecosystem and human health. The application of Saccharomyces cerevisiae (S. cerevisiae) for wastewater decolorization has been widely investigated due to their efficient removal and eco-friendly treatments. This review attempts to create an awareness of different forms and methods of using Saccharomyces cerevisiae (S. cerevisiae) for wastewater decolorization through a systematic approach. Overall, some suggestions on classification of dyes and related environmental/health problems, and treatment methods are discussed. Besides, the mechanisms of dye removal by S. cerevisiae including biosorption, bioaccumulation, and biodegradation and cell immobilization methods such as adsorption, covalent binding, encapsulation, entrapment, and self-aggregation are discussed. This review would help to inspire the exploration of more creative methods for applications and modification of S. cerevisiae and its further practical applications.
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Biodegradação Ambiental , Corantes , Saccharomyces cerevisiae , Saccharomyces cerevisiae/metabolismo , Corantes/metabolismo , Corantes/química , Águas Residuárias/química , Águas Residuárias/microbiologia , Poluentes Químicos da Água/metabolismo , Poluentes Químicos da Água/análise , Eliminação de Resíduos Líquidos/métodos , Descoloração da Água/métodosRESUMO
A novel method was used to synthesize benzimidazole-2-ones from the corresponding benzimidazolium salts. These salts were subsequently reacted with potassium tertiary butoxide (KOtBu), followed by oxidation using tertiary butyl hydrogen peroxide (TBHP) at room temperature in tetrahydrofuran (THF) to obtain the desired products in 1 h with excellent yields. After optimizing the reaction conditions, the study focused on preparing benzimidazole-2-ones with diverse substituents at N1 and N3 positions, including benzyl, 2',4',6'-trimethyl benzyl groups, and long-chain aliphatic substituents (hexyl, octyl, decyl, and dodecyl). The compounds were characterized by 1H and 13C NMR spectra, of which compound 2a is supported by single crystal XRD. Benzimidazole-2-one compounds exhibited promising anti-inflammatory and anti-cancer properties. The inhibition of mitochondrial Heat Shock Protein 60 (HSP60) of title compounds was also explored. Computational simulations were employed to assess anti-cancer properties of 19 benzimidazole-2-one derivatives (potential drugs). In-silico docking studies demonstrated promising binding interactions with HSP60, and these results were supported by molecular dynamics simulations. Notably, molecules 2b and 2d exhibited high affinity for HSP60 protein, highlighting their potential efficacy. The developed ligands were viable for the treatment of hepatocellular carcinoma (HCC). The findings provide valuable initial evidence supporting the efficacy of benzimidazole-2-ones as HSP60 inhibitors and lay the foundation for subsequent studies, including in-vitro assays.
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Benzimidazóis , Benzimidazóis/química , terc-Butil Hidroperóxido/química , Simulação de Acoplamento Molecular , Catálise , Antineoplásicos/química , Antineoplásicos/síntese química , Antineoplásicos/farmacologia , Simulação por ComputadorRESUMO
Indole-3-acetic acid (IAA) derived from Actinobacteria fermentations on agro-wastes constitutes a safer and low-cost alternative to synthetic IAA. This study aims to select a high IAA-producing Streptomyces-like strain isolated from Lake Oubeira sediments (El Kala, Algeria) for further investigations (i.e., 16S rRNA gene barcoding and process optimization). Subsequently, artificial intelligence-based approaches were employed to maximize IAA bioproduction on spent coffee grounds as high-value-added feedstock. The specificity was the novel application of the Limited-Memory Broyden-Fletcher-Goldfarb-Shanno Box (L-BFGS-B) optimization algorithm. The new strain AW08 was a significant producer of IAA (26.116 ± 0.61 µg/mL) and was identified as Streptomyces rutgersensis by 16S rRNA gene barcoding and phylogenetic inquiry. The empirical data involved the inoculation of AW08 in various cultural conditions according to a four-factor Box Behnken Design matrix (BBD) of Response surface methodology (RSM). The input parameters and regression equation extracted from the RSM-BBD were the basis for implementing and training the L-BFGS-B algorithm. Upon training the model, the optimal conditions suggested by the BBD and L-BFGS-B algorithm were, respectively, L-Trp (X1) = 0.58 %; 0.57 %; T° (X2) = 26.37 °C; 28.19 °C; pH (X3) = 7.75; 8.59; and carbon source (X4) = 30 %; 33.29 %, with the predicted response IAA (Y) = 152.8; 169.18 µg/mL). Our findings emphasize the potential of the multifunctional S. rutgersensis AW08, isolated and reported for the first time in Algeria, as a robust producer of IAA. Validation investigations using the bioprocess parameters provided by the L-BFGS-B and the BBD-RSM models demonstrate the effectiveness of AI-driven optimization in maximizing IAA output by 5.43-fold and 4.2-fold, respectively. This study constitutes the first paper reporting a novel interdisciplinary approach and providing insights into biotechnological advancements. These results support for the first time a reasonable approach for valorizing spent coffee grounds as feedstock for sustainable and economic IAA production from S. rutgersensis AW08.
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Inteligência Artificial , Ácidos Indolacéticos , RNA Ribossômico 16S , Streptomyces , Streptomyces/genética , Streptomyces/metabolismo , Ácidos Indolacéticos/metabolismo , RNA Ribossômico 16S/genética , Argélia , FilogeniaRESUMO
The permanent problem of formation of algal blooms in water polluted with nitrogen and phosphorus is one of the formidable environmental problems. Biochar has the potential to solve the issues related to eutrophication due to its special structure and ability to absorb the nutrients. Biochar's exceptional nutrient absorption capacity allows it to absorb excess nutrients, causing the algae to use fewer nutrients. This review deals with effective performance of biochar in reducing the effects caused by algal blooms and improving the environmental conditions. Besides, an analysis of the issues involved addresses the origins and consequences of nitrogen and phosphorus pollution, and the formation of algal blooms is also reviewed. It then delves deeply into biochar, explaining its properties, production methods, and their uses in environmental contexts. The review emphasizes that biochar can be effective in dealing with many challenges associated with environments affected by algal blooms, specifically focusing on the positive effects of biochar and algae to examine their roles in controlling algae growth. Finally, the review emphasizes new achievements and innovative ideas to foster sustainable aquatic ecosystems. The discussions emphasize the central role of biochar in managing nutrient-rich waters and algal blooms.
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Biodegradação Ambiental , Carvão Vegetal , Eutrofização , Fósforo , Fósforo/análise , Nitrogênio , EcossistemaRESUMO
Determining hazardous substances in the environment is vital to maintaining the safety and health of all components of society, including the ecosystem and humans. Recently, protein-based nanobiosensors have emerged as effective tools for monitoring potentially hazardous substances in situ. Nanobiosensor detection mode is a combination of particular plasmonic nanomaterials (e.g., nanoparticles, nanotubes, quantum dots, etc.), and specific bioreceptors (e.g., aptamers, antibodies, DNA, etc.), which has the benefits of high selectivity, sensitivity, and compatibility with biological systems. The role of these nanobiosensors in identifying dangerous substances (e.g., heavy metals, organic pollutants, pathogens, toxins, etc.) is discussed along with different detection mechanisms and various transduction methods (e.g., electrical, optical, mechanical, electrochemical, etc.). In addition, topics discussed include the design and construction of these sensors, the selection of proteins, the integration of nanoparticles, and their development processes. A discussion of the challenges and prospects of this technology is also included. As a result, protein nanobiosensors are introduced as a powerful tool for monitoring and improving environmental quality and community safety.
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Técnicas Biossensoriais , Monitoramento Ambiental , Substâncias Perigosas , Substâncias Perigosas/análise , Monitoramento Ambiental/métodos , Proteínas/análise , Nanoestruturas , Nanotecnologia , Nanopartículas/químicaRESUMO
Amoxicillin, a member of the penicillin family, is primarily utilized for the treatment of various bacterial infections affecting ears, nose, throat, urinary tract, and skin. Given its widespread application in medicine, agriculture, environment, and food industry, the precise and sensitive detection of amoxicillin is important. This study introduces a novel approach to developing a sensitive and selective fluorescent aptasensor relying on fluorescence resonance energy transfer (FRET) for the specific detection of amoxicillin. The carboxyfluorescein-labeled aptamer serves as a energy donor, while MXene functions as an energy acceptor, and acting as a quencher. To achieve optimal detection efficiency, a dual optimization strategy utilizing RSM-CCD and ANN-GA was used to fine-tune experimental conditions. The fluorescence measurements revealed an expansive linear range extending from 100 to 2400 ng mL-1, accompanied by an exceptionally low detection limit of 1.53 ng mL-1. Additionally, it shows an excellent selectivity towards amoxicillin over other antibiotics commonly found in water matrices. The aptasensor demonstrates good stability and reproducibility; effectiveness of the aptasensor was validated by testing in real water samples. This remarkable sensitivity and broad dynamic range affirm the efficacy aptasensor in accurately detecting varying concentrations of amoxicillin in wastewater bodies.
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Amoxicilina , Técnicas Biossensoriais , Amoxicilina/análise , Amoxicilina/química , Transferência Ressonante de Energia de Fluorescência/métodos , Aptâmeros de Nucleotídeos/química , Fluorescência , Poluentes Químicos da Água/análise , Água/químicaRESUMO
New photoactive materials with uniform and well-defined morphologies were developed for efficient and sustainable photoelectrochemical (PEC) water splitting and hydrogen production. The investigation is focused on hydrothermal deposition of zinc oxide (ZnO) onto indium tin oxide (ITO) conductive surfaces and optimization of hydrothermal temperature for growing uniform sized 3D ZnO morphologies. Fine-tuning of hydrothermal temperature enhanced the scalability, efficiency, and performance of ZnO-decorated ITO electrodes used in PEC water splitting. Under UV light irradiation and using eco-friendly low-cost hydrothermal process in the presence of stable ZnO offered uniform 3D ZnO, which exhibited a high photocurrent of 0.6 mA/cm2 having stability up to 5 h under light-on and light-off conditions. The impact of hydrothermal temperature on the morphological properties of the deposited ZnO and its subsequent performance in PEC water splitting was investigated. The work contributes to advancement of scalable and efficient fabrication technique for developing energy converting photoactive materials.
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Nanoestruturas , Óxido de Zinco , Óxido de Zinco/química , Água/química , Nanoestruturas/química , Compostos de Estanho/químicaRESUMO
A novel octahedral distorted coordination complex was formed from a copper transition metal with a bidentate ligand (1,10-Phenanthroline) and characterized by Ultraviolet-visible spectroscopy, Ultraviolet-visible diffuse reflectance spectroscopy, Fourier-transform infrared spectroscopy, Brunauer-Emmett-Teller, Field emission scanning electron microscopy, and Single-crystal X-ray diffraction. The Hirshfeld surface and fingerprint plot analyses were conducted to determine the interactions between atoms in the Cu(II) complex. DFT calculations showed that the central copper ion and its coordinated atoms have an octahedral geometry. The Molecular electrostatic potential (MEP) map indicated that the copper (II) complex is an electrophilic compound that can interact with negatively charged macromolecules. The HOMO-LUMO analysis demonstrated the π nature charge transfer from acetate to phenanthroline. The band gap of [Cu(phen)2(OAc)]·PF6 photocatalyst was estimated to be 2.88 eV, confirming that this complex is suitable for environmental remediation. The photocatalytic degradation of erythrosine, malachite green, methylene blue, and Eriochrome Black T as model organic pollutants using the prepared complex was investigated under visible light. The [Cu(phen)2(OAc)]·PF6 photocatalyst exhibited degradation 94.7, 90.1, 82.7, and 74.3 % of malachite green, methylene blue, erythrosine, and Eriochrome Black T, respectively, under visible illumination within 70 min. The results from the Langmuir-Hinshelwood kinetic analysis demonstrated that the Cu(II) complex has a higher efficiency for the degradation of cationic pollutants than the anionic ones. This was attributed to surface charge attraction between photocatalyst and cationic dyes promoting removal efficiency. The reusability test indicated that the photocatalyst could be utilized in seven consecutive photocatalytic degradation cycles with an insignificant decrease in efficiency.
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Cobre , Poluentes Ambientais , Cobre/química , Azul de Metileno/química , Cinética , Eritrosina , Luz , Corantes/química , CatáliseRESUMO
This study develops environmentally benign capping technique to synthesize nanoparticles of Curcuma longa-coated titanium dioxide (CR-TiO2) from titanium isopropoxide by utilizing the extract of Rosa rubiginosa flowers as reducing and chelating agent. The biogenically synthesized nanoparticles revealed excellent anti-bacterial, electrochemical, and photocatalytic properties due to the presence of porous TiO2 nanostructures. The sharp peaks by XRD pattern showed the crystallinity and phase purity of TiO2 nanoparticles. BET analysis proved mesoporous nature of the materials with specific surface area of 134 m2 g -1. The vibrational spectra suggest hydroxyl groups from flavonoids of Curcuma longa acting as functionalizing agent for TiO2 nanoporous structures with visible luminescence, which is proven in fluorescence spectra and is applicable for photocatalytic studies. The anti-bacterial studies showed good inference on TiO2 nanoparticles against Pseudomonas auruginosa and proved it to be an excellent antipseudomonal agent with the oxidative potential. The maximum degradation of phenol red dye in the presence of TiO2 under visible light conditions was observed. The supercapacitor fabricated using the biogenic TiO2 three-electrode system exhibited a specific capacitance of 128 Fg-1 (10 mV s-1), suggesting it as an excellent electrode material. The LSV curve at 50 mV s-1 scan rate showed that oxygen reduction potential (ORR) of CR-TiO2 electrodes was 121 mV. The present study is a new application of nanoparticles in sustainability consideration of the environment as well as a solution to the power crisis with fewer limitations. The well-distinguished antidiabetic and BSA denaturation potential suggests that these porous TiO2 nanostructures can be useful for drug delivery as glucose inhibitors and oral anti-inflammatory drugs with the restriction of adverse side effects.
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Antibacterianos , Nanoestruturas , Titânio , Titânio/química , Antibacterianos/química , Antibacterianos/farmacologia , Nanoestruturas/química , Catálise , PorosidadeRESUMO
The present study develops a novel concept of using waste media as an algal nutrient resource compared to the usual growth media with the aid of growth kinetics study and metabolite production abilities. Food- and agri-compost wastes are compact structures with elemental compounds for microbial media. As a part of the study, environ-burden wastes (3:1) as a food source for photosynthetic algae as a substitute for the costly nutrient media were proposed. The environment-burden waste was also envisaged for macromolecule production, i.e., 99200 µg/ml lipid, 112.5 µg/ml protein, and 8.75 µg/ml carbohydrate with different dilutions of agri-waste, bold basal media (BBM), and Food waste, respectively. The fabricated growth kinetics and dynamics showcased the unstructured models of different photosynthetic algal growth phases and the depiction of productivity and kinetic parameters. The theoretical maximum biomass concentration (Xp) was found to be more (0.871) with diluted agricompost media than the usual BBM (0.697). The XLim values were found to be 0.362, 0.323 and 0.209 for BBM, diluted agri-compost media and diluted food waste media, respectively. Overall, the study proposes a cleaner approach of utilizing the wastes as growth media through a circular economy approach which eventually reduces the growth media cost with integrated macromolecule production capabilities.
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Compostagem , Microalgas , Eliminação de Resíduos , Alimentos , Biocombustíveis , BiomassaRESUMO
In recent years, antibiotic drugs have been extensively used owing to increased industrial growth, and this has created issues related to drinking water and a green environment. Different techniques have been used to resolve these issues, among which heterogeneous photocatalysis has been widely explored for the elimination of toxic compounds from wastewater resources. In this study, ZnIn2S4, g-C3N4, and ZnIn2S4/g-C3N4 hybrid heterostructured composites are synthesized via hydrothermal method and used these (i) for the removal of antibiotic sulfamethoxazole pollutant and (ii) photoelectrochemical water oxidation. The nanomaterials were characterized using X-ray diffraction, Scanning electron microscopy, transmission electron microscopy, and UV-vis spectroscopy. The developed hybrid heterostructured composites were able to degrade sulfamethoxazole pollutants as well as offer improved photoelectrochemical properties compared to pristine samples. The catalytic performance of the materials developed under visible light irradiation was greatly improved for the degradation of the antibiotic drug up to 89.4% in 2 h. Moreover, the hybrid heterostructured photoelectrode showed a better photocurrent density (8.68 mA/cm2) and exhibited â¼19.2 and 29.9 times greater photocurrent density than the pristine photoelectrodes. Such a considerably increased catalytic activity was attributed to the active separation of charge carriers and transmission. The study offers an innovative approach to develop effective catalysts, and for the degradation of sulfamethoxazole as well as the PEC properties for hydrogen production.
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Antibacterianos , Poluentes Ambientais , Sulfametoxazol , Luz , Água , OxirreduçãoRESUMO
Photocatalytic dye degradation is a method of environmental degradation that is commonly used to eliminate various pollutants produced by pharmaceutical and textile industries. Herein, pure and chromium (Cr)-doped SnO2 nanoflakes were synthesized using a simple facile hydrothermal method and photocatalytic properties were studied under visible light illumination. In addition, photoelectrochemical (PEC) water oxidation properties were also studied using the prepared samples. Doping of transition metal ions introduces structural defects, which narrow the band gap of host sample, resulting in high catalytic activity. The synthesized doped SnO2 displayed a rutile tetragonal crystal phase with a nanoflakes-like surface morphology having no other contaminations. The optical band gap of Cr-doped SnO2 nanoflakes was significantly reduced (2.48 eV) over the pure sample (3.32 eV), due to successful incorporation of Cr ions into the host lattice. Furthermore, the dye removal efficiency of these nanoflakes was investigated for methyl orange (MO) and tetracycline (TC) organic contaminations. The Cr-doped SnO2 nanoflakes exhibited superior photodegradation with 87.8% and 90.6% dye removal efficiency, within 90 min of light illumination. PEC water oxidation analysis showed that the doped photoelectrode achieved enhanced photocurrent density and showed a higher photocurrent density (1.08 mA cm-2) over that of the undoped electrode (0.60 mA cm-2). Electrochemical impedance spectroscopy (EIS) showed that doped electrodes exhibited lesser charge resistance than the pure electrode. The synthesized Cr-doped SnO2 nanoflakes are suitable for water oxidation and photodegradation of organic pollutants. Thus, we strongly believe that the obtained results in this report will continue to provide new opportunities for the improvement of effective visible light photocatalysts for industrial wastewater treatment and water splitting for H2 generation.
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Poluentes Ambientais , Água , Água/química , Cromo , Oxirredução , LuzRESUMO
Engineered nanomaterials (ENMs) have been introduced into the market for a wide range of applications. As per the literature review, the fabrication of new generations of ENMs is starting to comply with environmental, economic, and social criteria in addition to technical aspects to meet sustainability criteria. At this stage, identification of the appropriate criteria for the synthesis of ENMs is critical because the technologies already developed at the lab scales are being currently transferred to pilot and full scales. Hence, the development of scientific-based methodologies to identify, screen, and prioritize the involved criteria is highly necessary. In the present manuscript, a fuzzy-Delphi methodology is adopted to identify the main criteria and sub-criteria encompassing the sustainable fabrication of ENMs, and to explore the "degree of consensus" among the experts on the relative importance of the mentioned criteria. The "health and safety risks" respecting the equipment and the materials, solvent used, and availability of "green experts" were identified as the most critical criteria. Furthermore, although all the criteria were identified as being important, some criteria, such as "solvent" and "raw materials cost", raised a lower degree of consensus, indicating that various "degrees of uncertainties" still exist regarding the level of importance of the studied criteria.
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Nanoestruturas , Projetos de Pesquisa , TecnologiaRESUMO
The worldwide energy calamity and ecological disturbances demand materials that can remove harmful contaminants from the polluted water. Recently, semiconductor-based catalytic dye removal has created much consideration due to its high efficacy and eco-friendly contaminated water treatment processes. Vanadium oxide (V2O5) has attracted superior attention as a catalyst due to its robust oxidation power, chemical inertness, and stability against photodegradation. In this study, pristine and cobalt (Co)-doped V2O5 samples were synthesized by solvothermal method and examined for their photo-degradation activity and photoelectrochemical (PEC) water oxidation properties. The orthorhombic crystal phase was confirmed by X-ray diffraction (XRD), hexagonal-shaped morphology was observed by scanning electron microscope (SEM) and reduced optical band gap (2.01 eV) was noticed for doped V2O5 catalyst compared to the pristine (2.20 eV) catalyst. The doped V2O5 catalyst exhibited enhanced photodegradation of crystal violet CV (92.7%) and Cr (VI) reduction (90.5%) after 100 min of light irradiation. The doped photocatalyst exhibited approximately 2.1 and 1.9-fold enhancement of photodegradation of CV and Cr(VI) reduction, respectively. The doped electrode showed improved photocurrent density (0.54 mA/cm-2) compared to pristine electrode (0.12 mA/cm-2). Moreover, the doped electrode showed reduced charge-transfer resistance and enhanced charge-transfer properties compared to those of the pristine electrode. Hence, the prepared hexagonal-shaped V2O5 is a suitable material for the elimination of environmental contaminants from the polluted water as well as water splitting for hydrogen generation.
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Cobalto , Poluentes Ambientais , Oxirredução , Óxidos/química , Fotólise , CatáliseRESUMO
Novel porous nanospheres from areca nuts (ACNPs) were synthesized via one-step pyrolysis without the use of any chemical treatment and the materials were used as adsorbents for the removal of cationic methylene blue (MB) and anionic methyl orange (MO) as well as their binary mixtures. Around, 6-7 tonnes of areca nut biowaste is generated every year which are then burnt due to their slow rate of decomposition resulting in higher carbon footprints. Biosorbents are generally a preferable alternative for dye adsorption but involve chemical modification for surface enhancement and complex sample treatment. In this work, ACNPs, were investigated for their efficiency in the raw form and were characterized by SEM, EDS, FTIR, XRD, and BET techniques before and after subjecting to the dye adsorption studies. The BET analysis of the adsorbents showed a high specific surface area of 693.8 m2/g when prepared at 1000 °C, while the N2 adsorption-desorption plot showed type-IV isotherm, suggesting the microporous nature of the carbon matrix. Batch equilibrium studies showed the removal efficiency of >95% for both the dyes and their binary mixtures under the optimum conditions of 0.15 g/L dosage, 10 µM concentration and contact time of 70 min. Due to the synergistic effects of the binary dyes, higher removal efficiency of MB compared to MO was observed in the binary mixture. Adsorption results were tested using Langmuir, Freundlich, Temkin, Redlich-Peterson, and Elovich isotherms to assess the best fit of the models. The qm value of MB was found to be 97.37 mg/g, while that of MO was 71.22 mg/g which is higher compared to individual dye components having lower values of 86.12 mg/g and 50.35 mg/g, respectively. Extended Langmuir and Jain and Snoeyink isotherms were used for binary data interpretation. The kinetic results showed good agreement with the Pseudo-second order equation, indicating internal diffusion. The possible mechanism involved electrostatic and á´¨-á´¨ interactions between the dye molecules and ACNPs. This approach is comprehensible and cost effective and can be utilized for dye removal in textile industries.
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Nanosferas , Poluentes Químicos da Água , Carbono/química , Corantes/química , Areca , Adsorção , Porosidade , Nozes/química , Análise Custo-Benefício , Poluentes Químicos da Água/análise , Cinética , Azul de Metileno/química , Concentração de Íons de HidrogênioRESUMO
Various catalysts in homogeneous or heterogeneous catalysis deploy unconventional reaction pathways by lowering the activation energy (AE) barrier, controlling the selectivity, and creating environmental impact, thereby bringing about economic viability. Hence, the study of these methodologies is of immense interest. To develop a new chemistry, there is much scope for the invention of brilliant candidates that could effectively catalyze diverse reaction methodologies. The palladium-catalyzed reactions motivate interesting applications on various organic transformations under mild reaction conditions. Although phosphorous designed ligands or catalysts have been used, despite their expensiveness, sensitivity and other properties, there is the necessity of developing even better cross-coupling ligands or catalysts such as N-heterocyclic carbene (NHC)-based palladium complexes. These palladium-NHCs (Pd-NHC) are novel and universal nucleophilic entities that have come into light as the most successful class of catalysts in organometallic chemistry. In the same class, a specific category of palladium-NHCs such as palladium-pyridine enhanced pre-catalyst preparation by the stabilization initiation (palladium-PEPPSI) complexes, are emerging as versatile alternatives to phosphine containing palladium complexes for various cross-coupling reactions due to their excellent catalytic activity. Further to mention that NHCs are recently extensively used as ancillary ligands in organometallic chemistry, which includes industrial-related catalytic transformations due to strong σ-donors to metal centres. Apart from this, many NHC-metal complexes are the fascinating consideration in material science as probable metallo-pharmaceuticals. The current review offers a brief exploration of palladium-PEPPSI complexes over the past few years. Further, the synthesis of a variety of these types of catalysts, their applications in Suzuki-Miyaura, Buchwald-Hartwig, Sonogashira, Negishi couplings direct C2-arylation, O-C(O) cleavage, α-arylation/alkylation of carbonyl compounds and trans-amidation reactions via cross-coupling methodologies, which are covered. Additionally, reported recent developments on reusable heterogeneous PdPEPPSI complexes and their catalytic applications are being covered. Finally, the chiral Pd complexes and their asymmetric transformations are discussed.
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Paládio , Piridinas , Paládio/química , Ligantes , CatáliseRESUMO
Excessive usage and unrestricted discharge of antibiotics in the environment lead to their accumulation in the ecosystem due to their highly stable and non-biodegradation nature. Photodegradation of four most consumed antibiotics such as amoxicillin, azithromycin, cefixime, and ciprofloxacin were studied using Cu2O-TiO2 nanotubes. Cytotoxicity evaluation of the native and transformed products was conducted on the RAW 264.7 cell lines. Photocatalyst loading (0.1-2.0 g/L), pH (5, 7 and 9), initial antibiotic load (50-1000 µg/mL) and cuprous oxide percentage (5, 10 and 20) were optimized for efficient photodegradation of antibiotics. Quenching experiments to evaluate the mechanism of photodegradation with hydroxyl and superoxide radicals were found the most reactive species of the selected antibiotics. Complete degradation of selected antibiotics was achieved in 90 min with 1.5 g/L of 10% Cu2O-TiO2 nanotubes with initial antibiotic concentration (100 µg/mL) at neutral pH of water matrix. The photocatalyst showed high chemical stability and reusability up to five consecutive cycles. Zeta potential studies confirms the high stability and activity of 10% C-TAC (Cuprous oxide doped Titanium dioxide nanotubes for Applied Catalysis) in the tested pH conditions. Photoluminescence and Electrochemical Impedance Spectroscopy data speculates that 10% C-TAC photocatalyst have efficient photoexcitation in the visible light for photodegradation of antibiotics samples. Inhibitory concentration (IC50) interpretation from the toxicity analysis of native antibiotics concluded that ciprofloxacin was the most toxic antibiotic among the selected antibiotics. Cytotoxicity percentage of transformed products showed r: -0.985, p: 0.01 (negative correlation) with the degradation percentage revealing the efficient degradation of selected antibiotics with no toxic by-products.
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Antibacterianos , Águas Residuárias , Antibacterianos/toxicidade , Ecossistema , Luz , Titânio/toxicidade , Titânio/química , Ciprofloxacina/toxicidade , CatáliseRESUMO
The 2,4-dichlorophenol (2,4-DCP) is an important chemical precursor that can affect human endocrine system and induce pathological symptoms. This research reports the degradation of 2,4-DCP using lab-scale hydrodynamic cavitation (HC) approach, which is considered a green and effective method. To promote the degradation efficiency, the zero-valent iron (Fe0) as the catalyst for sulfate radical (SO4â¢-) generation via activation of sulfite (SO32-) salts was simultaneously used. Degradation efficiency was favorable in acidic pH than the alkaline pH due to higher production of active radicals and was dependent on the dose of Fe0 and SO32-. Under optimal condition, degradation efficiency by Fe0/HC/sulfite (96.67 ± 2.90%) was considerably enhanced compared to HC alone (45.37 ± 2.26%). Quenching experiments suggested that SO4â¢-, â¢OH, 1O2, and O2â¢- radicals were involved in the degradation of 2,4-DCP by Fe0/HC/sulfite process, but the dominant role was related to â¢OH (70.09% contribution) and SO4â¢- (29.91% contribution) radicals. From the turbulence model, turbulent pressure at venturi throat decreased from -0.42 MPa to -2.02 MPa by increasing the inlet pressure from 1.0 to 4.0 bar and increase in pressure gradient has intensified bubble collapse due to higher turbulence tension.