Silver sulphide nanoparticles (Ag2SNPs) synthesized using Phyllanthus emblica fruit extract for enhanced antibacterial and antioxidant properties.

In this study, silver sulfide nanoparticles (Ag2SNP's) were successfully produced by using fruit extracts of Phyllanthus emblica. UV-vis, FTIR, XRD with SEM and EDX techniques were used for the synthesis process and for characterization of the resulting nanostructures. According to the findings, the fabricated nanostructure had a monoclinic crystal structure, measuring 44 nm in grain size, and its strain was 1.82 × 10-3. As revealed by SEM analysis, the synthesized nanostructure consists of irregular spherical and triangular shapes. The presence of silver (Ag) and sulfur (S) was also confirmed through EDX spectra. Furthermore, Ag2S nanoparticles were tested for their ability to effectively inhibit gram-positive and gram-negative bacterial growth. As a result of this study, it was clearly demonstrated that Ag2S nanoparticles possess powerful antibacterial properties, particularly when it came to inhibiting Escherichia coli growth. Ag2S nanoparticles had high total H2O2 and flavonoid concentrations and the greatest overall antioxidant activity, according to the evaluation of antioxidant activity of the samples. The results obtained from the P. emblica fruit extract were followed by those obtained from Ag2S nanoparticles were reported in detail. RESEARCH HIGHLIGHTS: Innovative Ag2SNP synthesis using Phyllanthus emblica fruit extract. SEM with EDX revealed a monoclinic crystal structure with a grain size of 44 nm and a strain of 1.82 × 10-3. Many of these applications are demonstrated by the potential of Ag2SNPs to treat and combat bacteria, particularly Escherichia coli. A peak at 653 cm-1 indicates the presence of primary sulfide aliphatic C-S extension vibrations. The abundant H2O2 and NO2 found in P. emblica nanocomposites make them potent antioxidants.

Reproducibility and long-term stability of Sn doped MnO2 nanostructures: Practical photocatalytic systems and wastewater treatment applications.

Sn-doped MnO2 were synthesized as an oxidant, a mediator of maleic acid (C4H4O4) and SnCl2 as doping ingredient via a basic sol-gel reaction with KMnO4. XRD study signposts that tetragonal crystal structure of MnO2 (ICDD#44-0141) with a plane group of 12/m (87) for both pure and Sn doped MnO2 nanostructures. The photocatalyst synthesized has mesoporosity, allowing to the N2 adsorption/desorption experiments. The geometry of the materials varies from spherical shape in pristine MnO2 to a rod-like shape in Sn-MnO2, as observed in the SEM and TEM pictures. To examine optic properties and energy bandgaps topologies, UV-visible diffuse reflectance spectroscopy was applied. In visible spectrum, overall catalytic performance of Sn-doped MnO2 was tested using methyl orange and phenol as dyes. The results suggest that the optimized Sn doped MnO2 (10 wt.%) catalyst showed higher degradation efficiency (98.5%), apparent constant (0.7841 min-1) and long term permanence. For this improved charge extraction efficiency, a potential photocatalytic mechanism was proposed.

Enhancing the photocatalytic performance of surface - Treated SnO2 hierarchical nanorods against methylene blue dye under solar irradiation and biological degradation.

Surfactant -treated tin oxide (SnO2) hierarchical nanorods were successfully synthesized through hydrothermal technique. The X-ray diffraction analysis showed the prepared SnO2 possesses tetragonal rutile structure having appreciable crystallinity with crystallite sizes in the range of 110 nm-120 nm. UV-visible diffuse reflectance absorption spectra confirm that the better visible light absorption band of SnO2 hierarchical nanorods have red shift compared to the pure SnO2. Fourier transform infrared spectroscopy (FTIR) study evident that the as-prepared SnO2 nanorods encompass the characteristic bands of SnO2 nanostructures. The morphological analyses of prepared materials were performed by FESEM, which shows that hierarchal nanorods and complex nanostructures. EDX analyses disclose all the samples are composed of Sn and O elements. The photocatalytic performance of the prepared surfactant treated SnO2 hierarchical nanorods was evaluated using methylene blue (MB) dye removal under direct natural sunlight. Recycling experiment results of CTAB - SnO2 nanorods and photocatalytic reaction mechanism also discussed in detail.

Effect of Ag doped MnO2 nanostructures suitable for wastewater treatment and other environmental pollutant applications.

A modest sol-gel method has been employed to prepare the pure and Ag doped MnO2 nanoparticles and methodologically studied their physical, morphological, and photosensitive properties through XRD, TEM, EDAX, Raman, UV, PL and N2 adsorption - desorption study. Tetragonal crystalline arrangement with spherical nanoparticles was found out through XRD and TEM studies. The EDAX studies further supported that formation Ag in the MnO2 crystal matrix. The bandgap energy of Ag doped MnO2 was absorbed through UV spectra. Photo -generated recombination process and surface related defects were further recognized by PL spectra. Through visible light irradiation, the photo - degradation of methyl orange (MO) and phenol dye solutions were observed. The optimum condition of (10 wt% of Ag) Ag doped MnO2 catalyst showed tremendous photocatalytic efficiency towards MO than phenol under same experimental study.

Optical and spectroscopic studies of potassium p-nitrophenolate dihydrate crystal for frequency doubling applications.

Non centrosymmetric potassium p-nitrophenolate dihydrate single crystals have been grown by employing the technique of slow solvent evaporation from aqueous solution by slightly adjusting the pH and growth temperature. The grown crystals have been identified from single crystal XRD analysis, FTIR and FT Raman spectroscopic techniques. The high resolution X-ray diffraction experiments substantiate good quality of the title material. Between 510 and 2000 nm, the material is observed to be nearly transparent allowing it to be explored for potential use in device fabrication. In addition, the photoluminescence spectrum of the grown crystal at room temperature shows a stable broad violet-blue emission around the 383-550 nm wavelengths with the maximum centered at 436 nm. Owing to its excellent non linear figure of merit and strong PL emission, the title crystal can have technological applications in opto-electronic devices.

Poly[tetra-aqua-bis(µ(2)-2,4,6-trinitro-phenolato)barium(II)].

The asymmetric unit of the title compound, [Ba(C(6)H(2)N(3)O(7))(2)(H(2)O)(4)](n), consists of a barium ion coordinated by two nitrophenolate ligands and four water mol-ecules. Barium is deca-coordinated by O atoms. These units are linked together through bridging nitro groups to form a one-dimensional polymeric chain. The three-dimensional packing is facilitated through hydrogen-bonding inter-actions mediated through water mol-ecules. The coordination distances around Ba vary from 2.728 (4) to 3.138 (5) Å. The crystal sample, on exposure to air at room temperature for many days, slowly loses the water and peels out as filaments.