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The sustainable management of wastewater and the production of clean fuel with a reduced carbon footprint require innovative methods, including photocatalytic degradation of pollutants and hydrogen generation. To achieve this, biosynthesized photocatalysts are necessary, with carbon quantum dots (CQDs) being a promising candidate for achieving this goal. In this study, CQDs were prepared from water caltrop peels and a composite of greenly synthesized CQDs with copper selenide (CuSe) was used for the photocatalytic degradation of pollutants and production of fuel. Thymol blue (TB) and Congo red (CR) were chosen as model dyes for degradation studies, with optimized reaction conditions being determined by varying the dose, pH, intensity, and concentration of dyes. The composite (CuSe@CQDs) showed a degradation rate of 99.4% and 97.8% for TB and CR, respectively, within 60 minutes, with a corresponding hydrogen production rate of 2360 and 1875 µmol g-1 h-1. The yield of hydrogen production using the composite was 35.7 and 29 times greater than that of CuSe alone for TB and CR, respectively. Spectroscopic techniques such as XRD, UV-Vis, FESEM, HRTEM, XPS, FTIR, BET, and TGA were used to characterize the composite, and the results revealed that the composite had superior degradation rates compared to CuSe alone, with the degradation rate being enhanced by about three times. GCMS analysis was used to investigate the intermediate and possible degradation pathways. Overall, this study highlights the potential of biosynthesized CQDs as effective photocatalysts for the sustainable management of wastewater and production of fuel.

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The preparation of polyaniline (PANI) and its copolymer with indole involved a chemical oxidative polymerization method, with benzene sulfonic acid (BSA, C6H6O3S) used as a dopant and potassium persulfate (PPS, K2S2O8) as an oxidant. The synthesized compounds underwent characterization using FTIR, 1H-NMR, TGA, and GPC techniques, which allowed the calculation of their average molecular weight and polydispersity index (PDI) through the GPC technique. The PDI values of the PANI copolymer with indole in different aniline-to-indole ratios were 1.53, 1.13, and 1.532 for 1:1, 1:2, and 2:1 ratios, respectively. Thermal stability was determined using TGA, revealing that the indole heterocyclic compound increased the inflexibility of the polymer chains in the synthesized PANI copolymer. The structure of the copolymer was further analyzed using 1HNMR and FTIR techniques, which confirmed the existence of benzenoid and quinoid groups in the PANI-indole copolymers, as well as the effect of doping on the polymer chains. The antibacterial and antifungal properties of the copolymers were studied against several bacterial and fungal strains and measured in terms of minimum inhibitory concentration. Results indicated that the inhibition rate of the PANI-indole copolymer on S. pyogenus (MTCC 442) was higher than that of standard drugs and individual PANI. The PANI-indole copolymers also displayed excellent antituberculosis and antimalarial activities, with the synthesized copolymer showing better outcomes than individual PANI.

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The study aimed to develop an efficient catalyst, biochar/Fe3O4@SiO2-Ag magnetic nanocomposite, to synthesize bioactive benzylpyrazolyl coumarin derivatives through a one-pot multicomponent reaction. The catalyst was prepared using Ag nanoparticles synthesized with Lawsonia inermis leaf extract and carbon-based biochar obtained through pyrolysis of Eucalyptus globulus bark. The nanocomposite contained a silica-based interlayer, highly dispersed Ag nanoparticles, and a central magnetite core, which responded well to external fields. The biochar/Fe3O4@SiO2-Ag nanocomposite showed excellent catalytic activity and could be easily recovered using an external magnet and reused five times without significant loss of performance. The resulting products were tested for antimicrobial activity and showed significant activity against various microorganisms.

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Graphene-based carbocatalysts owing to numerous amazing properties such as large specific surface area, high intrinsic mobility, excellent thermal and electrical conductivities, chemical stability, ease of functionalization, simple method of preparation, effortless recovery and recyclability have gained a superior position amongst the conventional homogeneous and heterogeneous catalysts. In this review, an endeavor has been made to highlight the syntheses of diverse heterocyclic compounds catalyzed by graphene-based catalysts. Further, the study also reveals that all the catalysts could be reused several times without significant loss in their catalytic activity. Additionally, most of the reactions catalyzed by graphene-based carbocatalysts were carried out at ambient temperature and under solvent-free conditions. Thus, the graphene-based catalysts do not merely act as efficient catalysts but also serve as sustainable, green catalysts. This review is divided into various sub-sections, each of which comprehensively describes the preparation of a particular heterocyclic scaffold catalyzed by graphene-derived carbocatalyst in addition to synthesis of graphene oxide and reduced graphene oxide, functionalization, and structural features governing their catalytic properties. Synthesis of heterocycles catalyzed by graphene-based carbocatalysts.

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Polyaniline (PANI) and its drug composites with some drugs like Neomycin (NM), Trimethoprim (TMP) and Streptomycin (ST) have been prepared by oxidative polymerization of aniline using hydrochloric acid (HA) and ammonium persulfate (APS) as a dopant and as an oxidant, respectively. The structures of PANI and PANI-drug composites were elucidated by FTIR and NMR spectroscopy, which confirmed the presence of benzenoid and quinoid rings in the synthesized compound. Molecular weight and thermal stability were determined by gel permeation chromatography (GPC) and thermogarvimetric analysis, respectively. From the GPC, PDI values of PANI-NM, PANI-TMP and PANI-ST were found to be 1.37, 1.23 and 1.56, respectively. For the study of antibacterial behavior of the synthesized PANI and PANI-drug composites, different micro-organisms, namely, four Gram positive (S. aureus MTCC 96, B. subtilis MTCC 441, S. pyogenes MTCC 442 and S. mutans MTCC 890) and four Gram negative (S. typhi MTCC 98, KL. pneumoniae MTCC 109, E. coli MTCC 443 and P. aeruginosa MTCC 1688) bacteria were selected due to their pharmacological importance. Some of the PANI-drug composites were found to show excellent results as compared to components polyaniline and drugs used for composite formation. Antituberculosis activity of the PANI and its drug composites against Mycobacterium tuberculosisH37RV (acid fast Bacilli) was determined. MIC values for PANI-NM and PANI-TMP were found to be 0.12 and 0.20 µg/mL, respectively. Results suggested that some of the drug composites may be tried as potential candidates for use as an antituberculoid agent to reduce TB transmission.

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AIM AND OBJECTIVE: Benzodiazepines and indole fused heterocycles are pharmacologically significant scaffolds. Trivial work on indole fused benzodiazepine compounds is reported in the literature. Hence, it is imperative to explore the synthesis of indole-fused benzodiazepines that may act as a template for biological studies in the future. Hence, in the present work, the synthesis of indole fused benzodiazepine derivatives was undertaken using multi-phase nano-titania as catalyst under microwave irradiation. MATERIALS AND METHODS: MAOS technique was used to carry out the synthesis of spiro-benzo [1,4]diazepine derivatives in the presence of multiphase nano-titania as a catalyst. Nano-titania was prepared by sol-gel method and characterized by XRD, FT-IR, FESEM, EDS and thermogravimetric techniques. The synthesized spiro-benzo [1,4] diazepine derivatives were identified by physical and spectral methods. RESULTS: Synthesized compounds were obtained in excellent yields in a short span of time. The synthesis was also carried out in the presence of conventional catalysts in addition to nano-titania. Among all the catalysts, the best result was obtained with nano-titania. The amount of nano-titania was optimized to be 0.05g giving 93- 95% yield of products. The study of reusability of nano-titania revealed that it could be reused up to four times with a negligible change in efficiency. CONCLUSION: The paper reports an efficient, cost-effective and environmentally benign approach for the synthesis of spiro-benzo [1,4] diazepine derivatives in the presence of multiphase nano-titania catalyst under microwave irradiation.

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The current research focuses on the photocatalytic, sonocatalytic and sonophotocatalytic degradation of nigrosine dye with nitrogen-doped and undoped zinc oxide powders. The sonophotocatalytic degradation of dye was found to occur at a higher rate than during photo- or sonocatalytic processes. Nitrogen-doped and undoped zinc oxide powders were synthesized by a wet chemical method. Further, scanning electron microscopy (FESEM), electron dispersive X-ray (EDX), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), UV-VIS spectroscopy (UV-VIS) and transmission electron microscopy (TEM) were used for the characterization of N-doped ZnO. The kinetics of nigrosine degradation were also studied and the results indicated that the degradation kinetics of nigrosine followed the first-order kinetics. The rate constant and the percentage of degradation were found to be highest, 7.33 × 10-4 (s-1) and 92% respectively, for sonophotocatalytic process after 90 min of reaction. Due to an increase in the available surface area or active sites of the catalyst, a higher rate constant and degradation efficiency was observed in the sonophotocatalytic system than in the photocatalysis system.

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