ZnO nanorods surface-decorated by WO3 nanoparticles for photocatalytic degradation of endocrine disruptors under a compact fluorescent lamp

Nanoscaled tungsten oxide (WO₃) particles coated on ZnO nanorods (ZNRs) were newly synthesized by combining a hydrothermal technique with a chemical solution process. The structure, morphologies and compositions of the as-prepared WO₃–ZNR nanocomposites were characterized through XRD, FESEM, TEM and Raman measurements. The results revealed that pure monoclinic WO₃ nanoparticles with an average size range of 18–26 nm were distributed on the surfaces of ZNRs and attached strongly. Particularly, the optical properties as well as photocatalytic characteristics of pure ZNRs and WO₃–ZNR nanocomposites with different loadings of WO₃ were also examined. The absorption of WO₃–ZNR nanocomposites was redshifted due to effective immobilization of WO₃ on ZNRs. Under irradiation of a 55 W compact fluorescence lamp, the photocatalytic activities of the WO₃–ZNR nanocomposites were superior to those of pure ZNRs and P25 in the degradation of resorcinol (ReOH). Furthermore, WO₃–ZNR nanocomposites showed very favorable recycle use potential and high sedimentation rate. Other endocrine disrupting chemicals (EDCs) such as phenol, bisphenol A (BPA) and methylparaben were also successfully photodegraded under identical conditions. These characteristics showed the practical applications of the WO₃–ZNR nanocomposites in indoor environmental remediation.     

Synthesis and Characterization of Molecularly Imprinted Polymer Membrane for the Removal of 2,4-Dinitrophenol

Molecularly imprinted polymers (MIPs) were prepared by bulk polymerization in acetonitrile using 2,4-dinitrophenol, acrylamide, ethylene glycol dimethacrylate, and benzoyl peroxide, as the template, functional monomer, cross-linker, and initiator, respectively. The MIP membrane was prepared by hybridization of MIP particles with cellulose acetate (CA) and polystyrene (PS) after being ground and sieved. The prepared MIP membrane was characterized using Fourier transform infrared spectroscopy and scanning electron microscopy. The parameters studied for the removal of 2,4-dinitrophenol included the effect of pH, sorption kinetics, and the selectivity of the MIP membrane. Maximum sorption of 2,4-nitrophenol by the fabricated CA membrane with MIP (CA-MIP) and the PS membrane with MIP (PS-MIP) was observed at pH 7.0 and pH 5.0, respectively. The sorption of 2,4-dinitrophenol by CA-MIP and PS-MIP followed a pseudo–second-order kinetic model. For a selectivity study, 2,4-dichlorophenol, 3-chlorophenol, and phenol were selected as potential interferences. The sorption capability of CA-MIP and PS-MIP towards 2,4-dinitrophenol was observed to be higher than that of 2,4-dichlorophenol, 3-chlorophenol, or phenol.     

One Step Synthesis of NiO Nanoparticles via Solid-State Thermal Decomposition at Low-Temperature of Novel Aqua(2,9-dimethyl-1,10-phenanthroline)NiCl2 Complex

[NiCl₂(C₁₄H₁₂N₂)(H₂O)] complex has been synthesized from nickel chloride hexahydrate (NiCl₂·6H₂O) and 2,9-dimethyl-1,10-phenanthroline (dmphen) as N,N-bidentate ligand. The synthesized complex was characterized by elemental analysis, infrared (IR) spectroscopy, ultraviolet-visible (UV-vis) spectroscopy and differential thermal/thermogravimetric analysis (TG/DTA). The complex was further confirmed by single crystal X-ray diffraction (XRD) as triclinic with space group P-1. The desired complex, subjected to thermal decomposition at low temperature of 400 ºC in an open atmosphere, revealed a novel and facile synthesis of pure NiO nanoparticles with uniform spherical particle; the structure of the NiO nanoparticles product was elucidated on the basis of Fourier transform infrared (FT-IR), UV-vis spectroscopy, TG/DTA, XRD, scanning electron microscopy (SEM), energy-dispersive X-ray spectrometry (EDXS) and transmission electron microscopy (TEM).     

Studies on the formation of yttrium iron garnet (YIG) through stoichiometry modification prepared by conventional solid-state method

Y₃Fe₅O₁₂ (YIG) prepared by conventional solid-state method can rarely be of high purity. However, this study suggests that high purity YIG can be produced via conventional solid-state methods, through stoichiometry modification. This is achieved by adding various amounts of excess Fe₂O₃ to control the YIG stoichiometric ratios. In this work, ferrite and yttria were calcined at 1100 °C (for 8 h) and sintered at 1420 °C (6 h). In most samples, the formation of YIG, with YFeO₃ (YIP) and/or Fe₂O₃ as associated phases were detected. Uniform microstructures of YIG are also observed. YIP phase in YIG is found to be inversely related to the addition of excess Fe₂O₃, up to 8 wt%. At above 8 wt% Fe₂O₃ addition, YIP disappears, leaving unreacted excess Fe₂O₃ as a new associated phase. From the investigation, it is safe to conclude that the purity of YIG can be increased with the addition of excess Fe₂O₃.     

Efficient conversion of light paraffinic naphtha to aromatics over metal-modified Mo/MFI catalysts

Journal of Porous Materials - The transformation of light naphtha to value-added aromatic compounds is gaining momentum in the petrochemical industry. In this work, a series of metal modified...     

Green Nanoarchitectonics of Cu/Fe3O4 Nanoparticles Using Helleborus niger Extract Towards an Efficient Nanocatalyst,Antioxidant and Anti-lung Cancer Agent

Biogenic nanoarchitectured magnetic materials have drawn serious attention throughout the last decade. We have attempted the Helleborus niger flower extract functionalized and templated biogenic synthesis of Cu nanoparticles supported Fe₃O₄ as a likewise novel material. The plant phytomolecules were deployed as a non-toxic sustainable reductant and an outstanding capping agent to stabilize the synthesized NPs. The synthesized Cu/H.niger@Fe₃O₄ nanocomposite was undergone comprehensive characterizations through Fourier transformed infrared spectroscopy (FT-IR), electron microscopy (SEM and TEM), energy dispersive X-ray spectroscopy (EDX), elemental mapping, vibrating sample magnetometer (VSM), X-ray diffraction (XRD) and inductively coupled plasma (ICP) techniques. The material was catalytically explored in the synthesis of diverse pyrano[3,2-c]chromene derivatives by coupling 4-hydroxycoumarin, malononitrile and a range of aldehydes in hot water when it afforded excellent yields. Based on its core magnetism, the catalyst was easily recovered using a magnet and reused for 8 successive times without considerable loss in catalytic activity. After the chemical application, the synthesized Cu/H.niger@Fe₃O₄ nanocomposite was engaged in biological assays like study of anti-oxidant properties by DPPH mediated free radical scavenging test using BHT as a reference molecule. Thereafter, on having a significant IC₅₀ value in radical scavenging assay, we extended the bio-application of the desired nanocomposite in anticancer study of A549 and H358 human lung cell lines in-vitro through MTT assay. The cell viability of malignant lung cell line reduced dose-dependently in the presence of desired nanocomposite. So, these results suggest that synthesized Cu/H.niger@Fe₃O₄ as a chemotherapeutic nanomaterial have a suitable anticancer activity against lung cell lines.

     

Novel Homozygous Missense Variant in GJA3 Connexin Domain Causing Congenital Nuclear and Cortical Cataracts

Congenital cataracts (CC) are responsible for approximately one-tenth of childhood blindness cases globally. Here, we report an African American family with a recessively inherited form of CC. The proband demonstrated decreased visual acuity and bilateral cataracts, with nuclear and cortical cataracts in the right and left eye, respectively. Exome sequencing revealed a novel homozygous variant (c.563A > G; p.(Asn188Ser)) in GJA3, which was predicted to be pathogenic by structural analysis. Dominantly inherited variants in GJA3 are known to cause numerous types of cataracts in various populations. Our study represents the second case of recessive GJA3 allele, and the first report in African Americans. These results validate GJA3 as a bona fide gene for recessively inherited CC in humans.     

Exploring the Bioactive Potentials of C60-AgNPs Nano-Composites against Malignancies and Microbial Infections

At present, the potential role of the AgNPs/endo-fullerene molecule metal nano-composite has been evaluated over the biosystems in-vitro. The intra-atomic configuration of the fullerene molecule (C₆₀) has been studied in-vitro for the anti-proliferative activity of human breast adenocarcinoma (MDA-MB-231) cell lines and antimicrobial activity against a few human pathogens that have been augmented with the pristine surface plasmonic electrons and antibiotic activity of AgNPs. Furthermore, FTIR revealed the basic vibrational signatures at ~3300 cm⁻¹, 1023 cm⁻¹, 1400 cm⁻¹ for O-H, C-O, and C-H groups, respectively, for the carbon and oxygen atoms of the C₆₀ molecule. NMR studies exhibited the different footprints and magnetic moments at ~7.285 ppm, explaining the unique underlying electrochemical attributes of the fullerene molecule. Such unique electronic and physico-chemical properties of the caged carbon structure raise hope for applications into the drug delivery domain. The in-vitro dose-dependent application of C₆₀ elicits a toxic response against both the breast adenocarcinoma cell lines and pathogenic microbes. That enables the use of AgNPs decorated C₆₀ endo fullerene molecules to design an effective anti-cancerous drug delivery and antimicrobial agent in the future, bringing a revolutionary change in the perspective of a treatment regime.     

Investigation on the effect of spinning conditions on the properties of hollow fiber membrane for hemodialysis application

Polyethersulfone (PES) hollow fiber membranes were fabricated via the dry‐wet phase inversion spinning technique, aiming to produce an asymmetric, micro porous ultrafiltration hollow‐fiber specifically for hemodialysis membrane. The objective of this study is to investigate the effect of spinning conditions on the morphological and permeation properties of the fabricated membrane. Among the parameters that were studied in this work are air gap distance, dope extrusion rate, bore fluid flow rate, and the take‐up speed. The contact angle was measured to determine the hydrophilicity of the fibers. Membrane with sufficient hydrophilicity properties is desired for hemodialysis application to avoid fouling and increase its biocompatibility. The influences of the hollow fiber's morphology (i.e., diameter and wall thickness) on the performance of the membranes were evaluated by pure water flux and BSA rejection. The experimental results showed that the dope extrusion rate to bore fluid flow rate ratio should be maintained at 1:1 ratio to produce a perfectly rounded asymmetric hollow fiber membrane. Moreover, the flux of the hollow fiber spun at higher air gap distance had better flux than the one spun at lower air gap distance. Furthermore, spinning asymmetric hollow fiber membranes at high air gap distance helps to produce a thin and porous skin layer, leading to a better flux but a relatively low percentage of rejection for BSA separation. Findings from this study would serve as primary data which will be a useful guide for fabricating a high performance hemodialysis hollow fiber membrane. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43633.