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In the present paper, activated nano-carbon soot is derived from atmospheric flame combustion of thymol-mustard oil followed by activation with potassium hydroxide (KOH) to produce micro- and mesoporous interiors. Different forms of activated nano-carbon soot are produced by using different weight percentage ratios 1:1, 1:3, and 1:5 of precursor carbon soot (CS) to KOH and named CS11, CS13, and CS15, respectively. An increase in specific surface area and average pore volume is observed with an increase in the amount of KOH with the hierarchical network having balanced micropores as well as mesopores in CS15. The electrochemical performance of prepared activated nano-carbon soot is further investigated by the fabrication of a symmetric electric double-layer solid-state supercapacitor (SC) device utilizing a 6 M KOH electrolyte. The CS15-based device displays the highest specific capacitance (Csp) of 226.20 F/g at a current density of 0.5 A/g with energy density (Ed) 31.42 Wh/kg at a power density (Pd) of 250 W/kg. The Csp, Ed, and Pd are found to be higher than activated nano-carbon soot reported in the literature. Further, three-coin cells are fabricated using CS15 which are tested in series combination with yellow light emitting diode (LED) and are found to be able to glow LED for ~ 5 min 25 s.
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The current research endeavour aimed to synthesize ferulic acid grafted tamarind gum/guar gum (FA-g-TG/GG) based powders as wound dressings, which could form in situ gels upon contact with wound exudates. In this context, variable amounts of FA were initially grafted with TG via the Steglich esterification reaction protocol and the resulting conjugates were subsequently amalgamated with GG and lyophilized to produce dry powders (F-1 - -F-3) with average particle size within 5.10-5.54 µm and average angle of repose â¼30°. These powders were structurally characterized with 1H NMR, FTIR, DSC, TGA, XRD and SEM analyses. Pristine TG, FA-g-TG and FA-g-TG/GG powders (F-2) revealed their distinct morphological structures and variable negative zeta potential values (-11.06 mV-25.50 mV). Among various formulation (F-1-F-3), F-2 demonstrated an acceptable powder-to-gel conversion time (within 20 min), suitable water vapour transmission rates (WVTR, 2564.94 ± 32.47 g/m2/day) and excellent water retention abilities and swelling profiles (4559.00 ± 41.57 %) in wound fluid. The powders were cytocompatible and conferred antioxidant activities. The powders also displayed fibroblast cell proliferation, migration and adhesion properties, implying their wound-healing potentials. Thus, the developed in situ gel-forming powders could be employed as promising dressings for wound management.
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Advanced graphene-based materials have been proficiently incorporated into next-generation solar cells and supercapacitors because of their high electrical conductivity, large surface area, excellent charge-transport ability, and exceptional optical properties. Herein, we report the synthesis of graphene nanosheets (GNs) from waste cardboard via pyrolysis, with ethyl alcohol as the growth initiator. Additionally, we demonstrated the use of GNs in energy conversion and storage applications. Using the GN electrode in perovskite solar cells resulted in an excellent power conversion efficiency of â¼10.41 % for an active area of 1 cm2, indicating an enhancement of approximately 27 % compared to conventional electrodes. Furthermore, the GNs were used as active electrode materials in supercapacitors with excellent electrochemical performance and a high gravimetric specific capacitance of 167.5 F/g at a scan rate of 2 mV/s. The developed GNs can be efficiently used for energy storage, conversion, and electrochemical sensing applications.
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Supercapacitors (SCs) are potentially trustworthy energy storage devices, therefore getting huge attention from researchers. However, due to limited capacitance and low energy density, there is still scope for improvement. The race to develop novel methods for enhancing their electrochemical characteristics is still going strong, where the goal of improving their energy density to match that of batteries by increasing their specific capacitance and raising their working voltage while maintaining high power capability and cutting the cost of production. In this light, this paper offers a succinct summary of current developments and fresh insights into the construction of SCs with high energy density which might help new researchers in the field of supercapacitor research. From electrolytes, electrodes, and device modification perspectives, novel applicable methodologies were emphasized and explored. When compared to conventional SCs, the special combination of electrode material/composites and electrolytes along with their fabrication design considerably enhances the electrochemical performance and energy density of the SCs. Emphasis is placed on the dynamic and mechanical variables connected to SCs' energy storage process. To point the way toward a positive future for the design of high-energy SCs, the potential and difficulties are finally highlighted. Further, we explore a few important topics for enhancing the energy densities of supercapacitors, as well as some links between major impacting factors. The review also covers the obstacles and prospects in this fascinating subject. This gives a fundamental understanding of supercapacitors as well as a crucial design principle for the next generation of improved supercapacitors being developed for commercial and consumer use.
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The pace of water contamination is increasing daily due to expanding industrialisation. Finding a feasible solution for effectively remediating various organic and inorganic pollutants from large water bodies remains challenging. However, a nano-engineered advanced hybrid material could provide a practical solution for the efficient removal of such pollutants. This work has reported the development of a highly efficient and reusable absorbent comprising a porous polyurethane (PU) and reduced graphene oxide (rGO) nanosheets (rGOPU) for the removal of different organic oils (industrial oil, engine oil and mustard oil), dyes (MB, MO, RB, EY and MV) and heavy metals (Pb(II), Cr(VI), Cd(II), Co(II) and As(V)). The structure, morphology and properties of the rGOPU hybrid absorbents were analysed by using Raman spectroscopy, field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA) and Brunner-Emitte-Teller (BET) analysis. The rGOPU possessed both superhydrophobicity and superoleophilicity with water and oil contact angles of about 164° and 0°, respectively. The prepared rGOPU has demonstrated an excellent oil-water separation ability (up to 99%), heavy metals removal efficiency (more than 75%), toxic dye adsorption (more than 55%), excellent recyclability (> 500 times for oils), extraordinary mechanical stability (90% compressible for > 1000 cycles) and high recoverability. This work presents the first demonstration of rGOPU's multifunctional absorbent capacity in large-scale wastewater treatment for effectively removing a wide variety of organic and inorganic contaminants.
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Grafite , Metais Pesados , Poluentes Químicos da Água , Poluentes da Água , Água/química , Grafite/química , Poluentes Químicos da Água/química , Adsorção , Cinética , Espectroscopia de Infravermelho com Transformada de FourierRESUMO
OBJECTIVES: The aim of this study was to investigate the potential of poly(amido amine) (PAMAM) dendrimer decorated graphene oxide (GO) based nanocarrier for targeted delivery of a hydrophobic anticancer drug, quercetin (QSR). METHODS: GO-PAMAM was successfully synthesized by covalent bonding between GO and NH2-terminated PAMAM dendrimer (zero generation). To investigate drug loading performance, QSR was loaded on the surface of GO as well as GO-PAMAM. Further, the release behaviour of QSR-loaded GO-PAMAM was studied. Finally, an in-vitro sulforhodamine B assay was performed in HEK 293T epithelial cells and MDA MB 231 breast cancer cells. KEY FINDINGS: It was observed that GO-PAMAM shows higher QSR loading capacity compared to GO. Also, synthesized nanocarrier exhibits controlled as well as pH-responsive release of QSR and the amount of QSR released at pH 4 was approximately two times higher than the release at pH 7.4. Furthermore, GO-PAMAM was found to be biocompatible for HEK 293T cells, and a high cytotoxic effect was observed for QSR-loaded GO-PAMAM on MDA MB 231 cells. CONCLUSIONS: The present investigation highlights the potential application of synthesized hybrid materials as a nanocarrier with excellent loading and controlled releasing efficiency for the delivery of the hydrophobic anticancer drug.
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Antineoplásicos , Neoplasias da Mama , Dendrímeros , Humanos , Feminino , Dendrímeros/química , Dendrímeros/farmacologia , Neoplasias da Mama/tratamento farmacológico , Quercetina/farmacologia , Antineoplásicos/farmacologia , Antineoplásicos/química , Concentração de Íons de Hidrogênio , Portadores de Fármacos/química , Sistemas de Liberação de MedicamentosRESUMO
Presently, carbon-based nanomaterials have shown tremendous potential for energy conversion applications. Especially, carbon-based materials have emerged as excellent candidates for the fabrication of halide perovskite-based solar cells, which may lead to their commercialization. In the last decade, PSCs have rapidly developed, and these hybrid devices demonstrate a comparable performance to silicon-based solar cells in terms of power conversion efficiency (PCE). However, PSCs lag behind silicon-based solar cells due to their poor stability and durability. Generally, noble metals such gold and silver are employed as back electrode materials during the fabrication of PSCs. However, the use of these expensive rare metals is associated with some issues, urgently necessitating the search for cost-effective materials, which can realize the commercial applications of PSCs due to their interesting properties. Thus, the present review shows how carbon-based materials can become the main candidates for the development of highly efficient and stable PSCs. Carbon-based materials such as carbon black, graphite, graphene nanosheets (2D/3D), carbon nanotubes (CNTs), carbon dots, graphene quantum dots (GQDs) and carbon nanosheets show potential for the laboratory and large-scale fabrication of solar cells and modules. Carbon-based PSCs can achieve efficient and long-term stability for both rigid and flexible substrates because of their high conductivity and excellent hydrophobicity, thus showing good results in comparison to metal electrode-based PSCs. Thus, the present review also demonstrates and discusses the latest state-of-the-art and recent advances for carbon-based PSCs. Furthermore, we present perspectives on the cost-effective synthesis of carbon-based materials for the broader view of the future sustainability of carbon-based PSCs.
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Multicomponent wastewater treatment utilising simple and cost-effective materials and methods is an important research topic. This study has reported the fabrication and utilisation of graphene oxide (GO) embedded granular Polyurethane (PU) (GOPU) adsorbent for the treatment of lead ion (Lead ion (Pb(II)), Methylene blue (MB), and E. coli. PU granules were wrapped with GO flakes to improve hydrophilicity, interaction with polluted water, cation-exchange reaction, and binding of pollutants on its surface. Synthesised GOPU granules were characterised by X-Ray Diffraction (XRD), Raman, Fourier transform infrared (FTIR) spectroscopy, and Scanning electron microscopy (SEM) analysis to ensure the successful synthesis of GO and fabrication of GOPU granules. Further, batch and continuous adsorption processes were studied in different operating conditions to evaluate the performance of GOPU granules in practical applications. The kinetic and isotherm analyses revealed that the adsorption of Lead (Pb(II)) ion and Methylene Blue (MB) dye followed the Freundlich and Langmuir isotherm models, respectively, and they showed good agreement with the Pseudo-second-order kinetic model. The adsorption capacities of GOPU granules for the elimination of Pb(II) and MB dye were about 842 mg/g and 899 mg/g, respectively. Additionally, investigations into the fixed bed column revealed that the adsorption column performed best at a flow rate of 5 mL/min and a bed height of 6 cm. Pb(II) adsorption had a bed uptake capacity (qbed) of 88 mg/g and percentage removal efficiency (%R) of 76%. Similarly, MB adsorption had a bed uptake capacity of 202 mg/g and a percentage removal efficiency of 71%. A systematic invention on antibacterial activity toward E. coli showed that The GOPU granules have a removal efficiency of about 100% at an exposure of 24 h. These findings indicated the possible use of GOPU granules as promising adsorbents for various water pollutants.
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Grafite , Poluentes Químicos da Água , Poluentes da Água , Chumbo , Poliuretanos , Azul de Metileno/química , Escherichia coli , Grafite/química , Poluentes Químicos da Água/análise , Adsorção , Cinética , Espectroscopia de Infravermelho com Transformada de Fourier , Concentração de Íons de HidrogênioRESUMO
BACKGROUND: The combinatorial use of anticancer drugs, dual or multiple, with a specific nanocarrier is one of the most promising attempts in drug delivery. The current work reports potassium contained graphene oxide (K-GO) as a nanocarrier in the drug delivery system of two anticancer drugs, gefitinib (GEF) and camptothecin (CPT), simultaneously. METHODS: To characterize K-GO, K-GO-related single and combined drug systems, different techniques have been performed and studied using the following spectroscopic tools, such as Thermo Gravimetric Analysis (TGA 4000), UV-visible spectroscopy, Raman spectroscopy, and Transmission electron microscopy (TEM). The in vitro cytotoxicity tests of K-GO, single drug system, and the combined drug system were also performed in the human breast cancer MDA-MB-231 cells. RESULTS: The release profile of the dual drug conjugates grafted onto the surface of K-GO was found to be up to 38% in PBS solution over 72 hours. The percentage of MDA-MB-231 cell viability was about 18% when treated with K-GO-GEF-CPT combined system; for K-GO, K-GO-GEF, and K-GO-CPT, the cell viability was 79%, 31%, and 32%, respectively. CONCLUSION: We studied the loading, release, and delivery of two anticancer drugs onto the fluorescent nanocarrier. Features, such as superb aqueous solubility, excellent biocompatibility, richness in potassium, and fluorescent nature, which can monitor the delivery of drugs, make them a promising nanocarrier for single or multiple drug delivery. Furthermore, our novel findings revealed that the loading capacity and cytotoxicity of the combined drug-loaded system are superior to the capacity of the individual drug system for human breast cancer cells.
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Antineoplásicos , Neoplasias da Mama , Grafite , Humanos , Feminino , Neoplasias da Mama/tratamento farmacológico , Preparações Farmacêuticas , Sistemas de Liberação de Medicamentos/métodos , Antineoplásicos/química , Gefitinibe , Portadores de Fármacos/químicaRESUMO
PCSK9 is a strongly expressed protein in the liver and brain that binds to the LDLR and regulates cholesterol in the liver effectively. Other receptors with which it interacts include VLDLR, LRP1, ApoER2, and OLR1. PCSK9 gain-of-function results in lysosomal degradation of these receptors, which may result in hyperlipidemia. PCSK9 deficiency results in a lower amount of cholesterol, which reduces cholesterol's accessibility to cancer cells. PCSK9 regulates several proteins and signaling pathways in cancer, including JNK, NF-κÐ, and the mitochondrial-mediated apoptotic pathway. In the liver, breast, lungs, and colon tissue, PCSK9 initiates and facilitates cancer development, while in prostate cancer cells, it induces apoptosis. PCSK9 has a significant impact on brain cancer, promoting cancer cell survival by manipulating the mitochondrial apoptotic pathway and exhibiting apoptotic activity in neurons by influencing the NF-κÐ, JNK, and caspase-dependent pathways. The PCSK9 impact in cancer at different organs is explored in this study, as well as the targeted signaling mechanisms involved in cancer growth. As a result, these signaling mechanisms may be aimed for the development and exploration of anti-cancer drugs in the immediate future.
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Neoplasias Encefálicas , Pró-Proteína Convertase 9 , Masculino , Humanos , Fígado , ApoptoseRESUMO
N-doped graphene stabilized Cu(I)-catalyzed self-healing nanocomposites are developed. This study found the use of N-doped graphene as both a nanostructured material for enhancing mechanical and conductive properties and a catalyst promoter (a scaffold for catalytic copper(I) particles), helpful to trigger self-healing via "click chemistry". Due to an increase in electron density on nitrogen atom doping, including the coordination of N-doped rGO with Cu+ ions, nitrogen-doped graphene-supported copper particles demonstrate a higher reaction yield at room temperature without adding any external ligand/base. In this study, only one component (an azide moiety containing a healing agent) was encapsulated, whereas another component (an alkyne moiety containing a healing agent) was as such (without encapsulation) homogeneously dispersed in a matrix. Triggered capsule rupture then induces the contact of the healing agents with the N-doped graphene-based catalyst and the alkyne molecules dispersed in the matrix, inducing a "click"-reaction, allowing onsite damage to be repaired as determined by mechanical measurements entirely. Tensile measurements were also performed using molecular dynamics (MD) simulations to support the findings. Given the enormous importance of autonomic repair of materials damage, this concept here reports a trustworthy and reliable chemical system with a high level of robustness.
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The aim to achieve sustainable development goals (SDG) and cut CO2-emission is forcing researchers to develop bio-based materials over conventional polymers. Since most of the established bio-based polymeric materials demonstrate prominent sustainability, however, performance, cost, and durability limit their utilization in real-time applications. Additionally, a sustainable circular bioeconomy (CE) ensures SDGs deliver material production, where it ceases the linear approach from production to waste. Simultaneously, sustainable circular bio-economy promoted materials should exhibit the prominent properties to involve and substitute conventional materials. These interceptions can be resolved through state-of-the-art bio-vitrimeric materials that display durability/mechanical properties such as thermosets and processability/malleability such as thermoplastics. This article emphasizes the current need for vitrimers based on bio-derived chemicals; as well as to summarize the developed bio-based vitrimers (including reprocessing, recycling and self-healing properties) and their requirements for a sustainable circular economy in future prospects.
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We report the effect of incorporating functionalized graphene oxide (terephthalic acid functionalized GO; GO-g-TPA) on the thermal and mechanical properties of Hytrel (HTL; a thermoplastic elastomeric polymer). Initially, the synthesis of GO-g-TPA was performed via chemical methods and subsequently characterized using various spectroscopic and imaging techniques. The melt mixing technique was executed in preparing the nanocomposites of HTL/GO and HTL/GO-g-TPA. An excellent GO dispersion was observed in the HTL polymeric matrix, which could be attributed to the significant effect of hydrogen bonding and π-π interaction between the HTL and GO-g-TPA. As a result of incorporating GO and GO-g-TPA into the HTL matrix, the overall mechanical and thermal properties of the nanocomposites were significantly improved. For the HTL/5 wt% GO-g-TPA nanocomposite, the tensile strength and storage modulus significantly increased by 61% and 224%, respectively. In addition, the melting temperature and crystalline temperature are increased by a notable 20 °C and 21 °C, respectively. Thus, the current study found that by improving the dispersion ability of the GO sheets, the properties of the HTL can be significantly enhanced and the prepared composite materials can be relevant for a wide range of applications including sports goods, hose jackets, wire and cable jackets, electronics, fluid power, sheeting belting seals, and footwear, etc.
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This study proposed a two-step method involving hydrothermal and electrostatic self-assembly processes for synthesising an amine-functionalised magnetic ligand graphene oxide-based nanocomposite (EDTA@Fe3O4@GO). The amine groups were successfully attached to the surface of iron (II, III) oxide (Fe3O4), which were embedded on the surface of graphene oxide (GO) (Fe3O4@GO). This EDTA@ Fe3O4@GO nanocomposite was used as a chelating agent to bind the toxic heavy metal ions. EDTA@Fe3O4@GO demonstrated the synergistic effect between the large surface area and magnetic behaviour of Fe3O4@GO and the chelating effect of EDTA, and it showed higher efficiency than the individual GO and Fe3O4. The possible structural and compositional characteristics were proposed based on Fourier transform infrared spectra (FTIR), X-ray diffraction (XRD), scanning electron microscope (SEM), Brunauer-Emmett-Teller (BET) and Raman spectroscopy analysis. The outcomes revealed the mechanism behind the excellent As(V) adsorption onto EDTA@Fe3O4@GO. The adsorption process was studied by fitting the experimental data obtained into various kinetic and isotherm models. The pseudo-second-order (PSO) kinetic model and the Freundlich isotherm model (FIM) were found to be the best fit models for the removal of As(V) by EDTA@Fe3O4@GO. EDTA@Fe3O4@GO has the utmost adsorption capacity of 178.4 mg/g. Furthermore, the EDTA@Fe3O4@GO nanocomposite is reusable, and it showed excellent adsorption capacity up to 5 cycles. This study has provided insight into the potential of EDTA@Fe3O4@GO and its applications in large-scale wastewater treatment.
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Grafite , Nanopartículas de Magnetita , Poluentes Químicos da Água , Ácido Edético , Aminas , Poluentes Químicos da Água/análise , Grafite/química , Adsorção , Cinética , Espectroscopia de Infravermelho com Transformada de FourierRESUMO
Assessing the interaction between microbes and nanocatalysts for finding an inclusive, proactive and deep understanding of nanoparticles-based toxicity is vital for discovering their broad range of applications. Palladium based photocatalysts owing to their unique fundamental characteristics and brilliant physicochemical potential have gained immense interest in environment remediation as disinfection system. In the present study, we report synthesis of a novel palladium nanoparticles decorated bismuth oxybromide (Pd/BiOBr) nanostructures using an energy efficient solution-based method, having excellent photocatalytic antibacterial action. The synthesized nanomaterials was thoroughly characterized using various analytical techniques. The photocatalytic antibacterial efficiency of Pd/BiOBr was evaluated against some common pathogenic strains of Gram-positive and Gram-negative bacteria (Pseudomonas fluorescens, Pseudomonas aeruginosa, Escherichia coli, Aeromonas salmonicida, Salmonella typhimurium, Klebsiella pneumoniae, Bacillus subtilis). In our results Pd/BiOBr showed excellent photocatalytic disinfection efficacy with > 99.9% bacterial inactivation. A very low concentration of Pd/BiOBr (0.5 µg/mL) effectively inhibited the bacterial growth in response to just 2 h of visible light irradiation, while 1 µg/mL of Pd/BiOBr completely killed all the tested bacterial strains proving their magnificent bactericidal potential. The developed materials with exceptional antibacterial broad range efficiency can be used in different photocatalytic disinfection systems including water purification systems, biofilm exclusion and combating differential antibiotic resistance.
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Nanopartículas Metálicas , Paládio , Antibacterianos/química , Antibacterianos/farmacologia , Bismuto/química , Bismuto/farmacologia , Catálise , Escherichia coli , Bactérias Gram-Negativas , Bactérias Gram-Positivas , Luz , Paládio/farmacologiaRESUMO
Herein, we report a robust approach for the selective covalent functionalization of graphene oxide (GO) with 4-hydroxybenzoic acid (HBA) for developing polymeric nanocomposites based on liquid crystalline polymers (LCPs). The functionalization of GO with HBA was confirmed by Raman spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, and X-ray diffraction (XRD) spectroscopy. The surface morphology of GO and functionalized GO (FGO) was studied using field emission scanning electron microscopy (FE-SEM). Furthermore, the interactions between FGO and LCPs have been investigated by FT-IR spectroscopy, whereas dispersion of GO and FGO in the LCP matrix was analyzed by FE-SEM. The better dispersion of FGO can be attributed to the hydrogen bonding and π-π stacking interactions between FGO and LCPs. Our results showed that even the addition of 5 wt% FGO in the LCP matrix significantly enhances the tensile strength and storage modulus of the pristine LCPs by 84% and 78% respectively. Compared to neat LCPs, FGO incorporated composites also demonstrate an improvement in the melting temperature (Tm) by 11 °C and glass transition temperature (Tg) by 12 °C. Furthermore, thermogravimetric analysis (TGA) was performed to evaluate the thermal stability of the composite. The 5 and 50% decomposition temperature for the LCP/FGO nanocomposites (containing 5 wt% FGO) increased by 75 °C and 107 °C respectively.
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In this work, polymer grafted magnetic graphene oxide (GO-PVP-Fe3O4) was successfully synthesized for efficient delivery of anticancer drug. Firstly, GO was functionalized with the hydrophilic and biocompatible polymer polyvinylpyrrolidone (PVP) and then grafted with magnetic nanoparticles (Fe3O4) through an easy and effective chemical co-precipitation method. Quercetin (QSR) as an anticancer drug was loaded onto the surface of GO-PVP-Fe3O4 via non-covalent interactions. The drug loading capacity was as high as 1.69 mg mg-1 and the synthesized magnetic nanocarrier shows pH-responsive controlled release of QSR. The cellular cytotoxicity of the synthesized nanocarrier with and without drugs was investigated in human breast cancer MDA MB 231 cells and their effects compared on non-tumorigenic epithelial HEK 293T cells. These results reveal that the drug loaded GO-PVP-Fe3O4 nanohybrid was found to be more toxic than the free drug towards MDA MB 231 cells and exhibits biocompatibility towards HEK 293T cells. Overall, a smart drug delivery system including polymer grafted magnetic graphene oxide as a pH-responsive potential nanocarrier could be beneficial for targeted drug delivery, controlled by an external magnetic field as an advancement in chemotherapy against cancer.
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Upcycling waste into value-added products for utilization in wastewater abatements has been explored in a number of treatment technologies. One such waste, single-use plastic, which poses significant adverse environmental and economic impact, has been chosen and converted into graphitic carbon to reduce the waste burden sustainably and economically. The sorptive and catalytic performance of synthesized plastic waste-derived carbon (PWC) was evaluated using brilliant green (BG) and eosin yellow (EY) as target pollutants. The adsorption capacity of PWC was very low for BG (7.41 mg/g) and EY (4.93 mg/g). The coupling of PWC with peroxymonosulfate (PMS) promoted dye degradation. Complete degradation of the dye, with ~61% reduction in TOC and ~95% reduction in toxicity, was achieved by oxidative treatment (initial concentration: 10 mg/L). The functionalities of PWC facilitated better electron transfer to PMS for its effective activation, which led to the production of SO4â¢- and OHâ¢. The quenching study confirmed that the degradation of dyes was primarily due to SO4â¢-. Additionally, the pathways of dye degradation were proposed based on the intermediates identified. Thus, this study established the high potential of PWC as a metal-free catalyst in PMS activation for the abatement of organic pollutants.
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Carvão Vegetal , Poluentes Ambientais , Carbono , Catálise , Corantes , Peróxidos , PlásticosRESUMO
Natural products have widely been used in applications ranging from antibacterial, antiviral, antifungal, and various other medicinal applications. The use of these natural products was recognized way before the establishment of basic chemistry behind the disease and the chemistry of plant metabo-lites. After the establishment of plant chemistry, various new horizons evolved, and the application of natural products breached the orthodox limitations. In one such interdisciplinary area, the use of plant materials in the synthesis of nanoparticles (NPs) has exponentially emerged. This advancement has offered various environment-friendly methods where hazardous chemicals are completely replaced by natural products in the sophisticated and hectic synthesis processes. This review is an attempt to under-stand the mechanism of metal nanoparticles synthesis using plant materials. It includes details on the role of the plant's secondary metabolites in the synthesis of nanoparticles including the mechanism of action. In addition, the use of these nanomaterials has widely been discussed along with the possible mechanism behind their antimicrobial and catalytic action.
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Anti-Infecciosos , Produtos Biológicos , Nanopartículas Metálicas , Antibacterianos/farmacologia , Anti-Infecciosos/farmacologia , Química Verde , Extratos Vegetais/farmacologiaRESUMO
The room temperature synthesis of an all-solid-state Z-scheme CuO-doped BiOBr (CuO-Bi-BiOBr) photocatalyst has been described. These CuO-Bi-BiOBr ternary heterojunctions exhibit efficient photocatalytic activities for selective alcohol oxidation. The structures, morphologies, and compositions of the nanostructures were well characterized using field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and atomic absorption spectroscopy (AAS). The X-ray diffraction (XRD) pattern of the as-synthesized nanostructures confirms the formation of phase-segregated CuO and BiOBr nanocrystals, whereas X-ray photoelectron spectroscopy (XPS) and high-resolution transmission electron microscopy (HRTEM) analyses clearly indicate the formation of metallic bismuth nanoparticles (NPs). Next, the developed CuO-Bi-BiOBr ternary heterojunctions were applied as an efficient photocatalyst for the oxidation of alcohols into their corresponding aldehydes/ketones with high selectivity (>99%) and high conversion ratios (>99%). Herein, Bi metal NPs act as an electron mediator and bridge the connectivity between the two semiconductors, BiOBr and CuO, and, thus, a Z-scheme heterojunction is established. As expected, CuO-Bi-BiOBr has shown significantly superior activities compared to those of pure BiOBr. A possible mechanism for the photocatalytic oxidation process has been proposed. Radical scavenging experiments suggest that the active species, h+, ËOH, e-, and ËO2-, are dominant in the alcohol oxidation process. The as-synthesized CuO-Bi-BiOBr was reused several times without any significant deterioration in the original activities and it thus possesses relatively high stability for practical applications.