This study involves the fabrication of mixed matrix membranes (MMMs) for ultrafiltration, which contained 3‐aminopropyltriethoxysilane modified magnetite iron oxide nanoparticles (A‐Fe3O4 NPs), through a modified phase inversion technique. The physiochemical properties and surface morphologies of both the as‐synthesized A‐Fe3O4 NPs and fabricated MMMs were examined using advanced characterization techniques. The quasi‐spherical A‐Fe3O4 NPs had an average particle size of 12 nm and a Brunauer–Emmett–Teller surface area of 131.38 m2/g. Analysis by Fourier transform infrared and Raman spectroscopy confirmed the presence of NH2 and OH functional groups grafted onto the Fe3O4 NPs. The incorporation of higher loadings of A‐Fe3O4 NPs in the membrane matrix significantly improved the adsorptive ability and hydrophilicity of the adsorbent, leading to improved membrane water permeance, adsorption rate, and adsorption‐filtration properties. The water contact angle decreased from 70.7° to 63.2°, and the flux increased from 239.9 to 443.8 L/m2.h, while overall membrane porosity increased from 43.4% to 51.9%.

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Present work reports synthesis of L-cysteine capped CdSe nanoparticles at different temperatures via an aqueous medium, non-toxic and green colloidal route. Cadmium chloride (CdCl2·5H2O) and sodium selenite (Na2SeO3) were used as cadmium and selenium sources respectively. The prepared nanoparticles are characterized by UV-visible absorption and photoluminescence spectroscopy, Fourier transform infrared, X-ray diffraction and transmission electron microscopy. The XRD patterns confirm a cubic phase structure of the prepared nanoparticles at 55, 75 and 95 ºC, respectively. The TEM analysis, optical absorption and photoluminescence spectra shows epitaxial growth of CdSe nanoparticles as the temperature increases with average size diameter of 4.12 ± 0.32, 5.02 ± 0.234 and 5.53 ± 0.321 nm for 55, 75 and 95 ºC, respectively.