Synthesis of nitrogen doped carbon quantum dots/magnetite nanocomposites for efficient removal of methyl blue dye pollutant from contaminated water

As a remedy for environmental pollution, a simple synthesis approach has been developed to prepare nitrogen doped carbon quantum dot/magnetite nanocomposites (Fe₃O₄@NCQDs NCs) using non-toxic and cost effective lemon juice as precursor for removal of organic dye pollutant. Fe₃O₄@NCQDs NCs were characterized by using UV-Vis spectroscopy, FTIR, XRD, FESEM, EDS, TEM, VSM and TGA/DTA. TEM results show spherical shaped Fe₃O₄@NCQDs NCs with an average particle size of 5 nm. Batch adsorption studies were done to investigate the tendency of the nanocomposites to remove representative methyl blue (MB) dye from aqueous solution. The effects of MB dye concentration, dosage of Fe₃O₄@NCQDs NC adsorbent, pH, contact time and temperature were optimized by varying one variable while all the other parameters were kept constant. The experiment showed rapid removal of MB dye within 20 minutes with an adsorption efficiency of over 90.84% under optimum conditions. The adsorption process fits the Freundlich isotherm model well with R² and n values of 0.993 and 1.842, respectively, at 298 K indicating the feasibility of the adsorption process. The adsorption process is spontaneous and involves exothermic behaviour as confirmed by thermodynamic studies. From a kinetic study, it was found that the pseudo-second order model is more suitable to describe the adsorption process than the pseudo-first order model for adsorption of MB dye onto Fe₃O₄@NCQDs NCs.

Herein, we report the green synthesis of magnetic, nitrogen doped carbon quantum dot/Fe₃O₄ NPs using aqueous lemon extract for the efficient removal of organic dye pollutants from contaminated water.     

Hydrothermal green synthesis of MoS2 nanosheets for pollution abatement and antifungal applications

In this study, we report a green synthesis of MoS₂ nanosheets (NSs) using a facile hydrothermal technique in the presence of l-cysteine. l-Cysteine can serve as a greener source of sulfur as well as a capping agent to help the growth of MoS₂ nanosheets. The prepared materials were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS), electron transmission microscopy (TEM), X-ray photoelectron microscopy (XPS), and Brunauer, Emmett, and Teller (BET) analysis. The results showed that MoS₂ NSs are of high crystallinity with a lattice spacing of 0.61 nm. The optical bandgap of MoS₂ NSs nanosheets prepared using l-cysteine as a source of sulfur was found to be 1.79 eV. The photocatalytic degradation of MoS₂ NSs towards methylene orange (MO) and rhodamine blue (RB) dyes under sunlight was found to be promising for practical applications. The fast kinetics of degradation of MO and RhB was observed over a wide range of pH range. Moreover, MoS₂ NSs showed excellent antifungal activities against Trichophyton mentagrophytes and Penicillium chrysogenum fungus.

In this study, we report a green synthesis of MoS₂ nanosheets (NSs) using a facile hydrothermal technique in the presence of l-cysteine.     

Green synthesis of zinc oxide nanostructures and investigation of their photocatalytic and bactericidal applications

We report a facile one-pot green synthesis of zinc oxide (ZnO) nanostructures using aqueous leaf extract of Dolichos Lablab L. as the reducing and capping agent. The optical properties, structure and morphology of the as-synthesized ZnO nanostructures have been characterized by UV-Visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) supported with energy dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). TEM analysis revealed that the as-synthesized ZnO nanostructures have an average particle diameter of 29 nm. XRD patterns confirmed the formation of phase-pure ZnO nanostructures with a hexagonal wurtzite structure. The synthesized ZnO nanostructures were used as a catalyst in the photodegradation of methylene blue (MB), rhodamine B (RhB) and orange II (OII) under visible and near-UV irradiation. The results showed the highest efficiency of photodegradation of ZnO nanostructures for MB (80%), RhB (95%) and OII (66%) at pH values of 11, 9 and 5, respectively, in a 210 min time interval. In addition, the antimicrobial activity of the ZnO nanostructures using the agar well diffusion method against Bacillus pumilus and Sphingomonas paucimobilis showed the highest zones of inhibition of 18 mm and 20 mm, respectively. Hence, ZnO nanostructures have the potential to be used as a photocatalyst and bactericidal component.

We report a facile one-pot green synthesis of zinc oxide (ZnO) nanostructures using aqueous leaf extract of Dolichos Lablab L. as the reducing and capping agent.     

Molecular analyses of novel ASAH1 mutations causing Farber lipogranulomatosis: analyses of exonic splicing enhancer inactivating mutation

Farber lipogranulomatosis is a rare autosomal recessive lysosomal storage disorder caused by mutations in the ASAH1 gene. In the largest ever study, we identified and characterized ASAH1 mutations from 11 independent Farber disease (FD) families. A total of 13 different mutations were identified including 1 splice, 1 polypyrimidine tract (PPT) deletion and 11 missense mutations. Eleven mutations were exclusive to the Indian population. The IVS6+4A>G splice and IVS5‐16delTTTTC PPT deletion mutations resulted in skipping of exon 6 precluding thereby the region responsible for cleavage of enzyme precursor. A missense mutation (p.V198A) resulted in skipping of exon 8 due to inactivation of an exonic splicing enhancer (ESE) element. This is the first report of mutations affecting PPT and ESE in the ASAH1 gene resulting in FD.     

Vitamin C assisted synthesis of rGO–Ag/PANI nanocomposites for improved photocatalytic degradation of pharmaceutical wastes

A highly efficient visible light active polyaniline (PANI)/Ag composites grafted reduced graphene oxide (rGO–Ag/PANI) was prepared for the efficient photocatalytic degradation of paracetamol. The structural, morphological, and light absorption properties of the as-synthesized rGO–Ag/PANI were characterized by UV-Visible (UV-Vis) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Paracetamol was taken as a model water pollutant to investigate the photocatalytic degradation efficiency of the rGO–PANI/Ag nanocomposites under visible light radiation. The result shows the degradation of paracetamol to be 99.6% in the acidic medium (pH 5) and 75.76% in the basic medium (pH 9), respectively. The enhanced degradation efficiency is attributed to the synergetic effect of rGO, PANI, and Ag NPs in the nanocomposites. This synergy of the rGO–Ag/PANI is explained by the strong adsorption efficiency, charge separation, and light absorption in the visible region.

A highly efficient visible light active polyaniline (PANI)/Ag composites grafted reduced graphene oxide (rGO–Ag/PANI) was prepared for the efficient photocatalytic degradation of paracetamol.