Usama Zulfiqar

Fabrication of superhydrophobic filter paper and foam for oil–water separation based on silica nanoparticles from sodium silicate

We demonstrate the synthesis of hydrophobic silica nanoparticles from sodium silicate and their application in separation of the oil–water mixture. For this, hydrophobic silica nanoparticles of size 35 ± 8 nm were initially synthesized by sol–gel method using sodium silicate and trimethylchlorosilane, and further deposited on commercially available filter paper and polyurethane foam by dip coating technique. The coating cycles were optimized for filter paper to ensure that fibers of the filter paper have been completely covered with hydrophobic silica nanoparticles to provide an ideal porous superhydrophobic/superoleophilic framework for gravity based separation of oil–water mixtures. It was confirmed by water contact angle of ~155° and sliding angle <5°. Whereas the superhydrophobic polyurethane foam was utilized for collection of oil from oil–water mixtures via absorption. The capability of these materials to separate oil from water was tested against the mixtures of water with n-hexane, gasoline, diesel, kerosene oil and engine oil. Moreover, the produced particles can also be used for fabrication of semi-transparent superhydrophobic surfaces.Graphical Abstract

Synthesis and characterization of silica nanoparticles from clay

Abstract We report a method to synthesize silica nanoparticles from bentonite clay. A series of thermal and acid treatment processes was performed on bentonite clay to lower the alumina and increase the silica content. The obtained silica rich clay was treated in two different concentrations (10 wt% and 40 wt%) with sodium hydroxide solution to form sodium silicate solutions (SSS). One type of SSS was hydrolyzed with three different concentrations (5 M, 10 M and 15 M) of nitric acid in the presence of ethanol as cosolvent while the other SSS was hydrolyzed with nitric acid in the presence of three different quantities (10 ml, 20 ml and 30 ml) of ethanol as cosolvent. A range of silica particle sizes from nanometer to micrometer was obtained by varying the contents of silica rich clay, HNO3, and ethanol. It was observed that the concentration of silica rich clay and HNO3 had a direct effect on the particle size. The increase in the quantity of ethanol from 10 ml to 20 ml produced bimodal particles of nanometer and micrometer size, which maintained at 30 ml. Inductively coupled plasma optical emission spectroscopy, atomic absorption spectroscopy, X-ray fluorescence, scanning electron microscopy and X-ray diffraction were utilized to characterize the clay, SSS and nanoparticles.

Synthesis of silica nanoparticles from sodium silicate under alkaline conditions

Abstract Compared to the synthesis of silica nanoparticles from tetraethyl orthosilicate, its synthesis from sodium silicate solution (SSS) in alkaline medium is less investigated. Herein, we present a study for the synthesis of non-agglomerated silica nanoparticles from SSS under alkaline conditions. SSS was diluted with water and slowly added in the mixture of ethanol and ammonia to form a sol which was aged and centrifuged to obtain silica nanoparticles. Effect of different ratios of ethanol and ammonia in the mixture on the size of silica nanoparticles was studied, and these nanoparticles were characterized using scanning electron microscopy, Fourier transformation infrared spectroscopy and X-ray diffraction techniques. It was found that the produced silica nanoparticles were spherical in shape, non-agglomerated in nature and their size could be tailored with the change in the ratio of ammonia and ethanol.Graphical Abstract

A comprehensive study on the surface chemistry of particulate matter collected from Jeddah, Saudi Arabia

In this work, the X-ray Photoelectron Spectroscopy (XPS) technique is utilized to analyze the surface chemical composition of particulate matter (PM) which was collected from various locations at Jeddah, Saudi Arabia. The main elements found on the surface of PM are carbon (C), oxygen (O) and silicon (Si) with combined percentage of 89.4–94.9 while traces of nitrogen (N), calcium (Ca), aluminum (Al), sodium (Na), chlorine (Cl), manganese (Mg), and sulfur (S) were also present. The analyzed XPS chemical state of C, O and Si was further used to determine their bonding with other elements occurring over the surface of PM. Carbon was found in the form of carbides (18.86%), fluorides (2.39%) and carbonates (78.75%); oxygen was observed as oxides (21.05%) and hydroxides (73.42%) of other metals; and silicon was detected as silicones (12.16%), nitrides (82.53%) and silicates (5.25%). The particle size of a PM is also of great concern for health issues, and thus has been investigated by the Field Emission Scanning Electron Microscope (FESEM). The Energy Dispersive X-ray Spectroscopy (EDS) was employed for cross verification of detected elements by XPS.

Improving the performance of conventional glass fiber epoxy matrix composites by incorporating nanodiamonds

Abstract Multiscale glass fiber epoxy matrix composites containing nanodiamonds were fabricated using vacuum bagging technique. Three different loadings of nanodiamonds were incorporated in epoxy resin after their functionalization through ozone-treatment, i.e., 0.1, 0.3 and 0.5 wt%. The functionalization of nanodiamonds was confirmed by infrared spectroscopy, which improved the dispersion of nanodiamond in epoxy resin thus improving the mechanical properties. Tensile, compression, flexural and interlaminar shear properties of the composites were improved. The tensile, compression and flexural strengths improved up to 36, 56 and 30% by the addition of 0.5 wt% nanodiamonds while the corresponding moduli increased to 30, 125 and 46%, respectively. An improvement of 38% in interlaminar shear strength was observed. The microscopy of the composites was performed using optical and electron microscopy and proper impregnation of glass fibers and the absence of the agglomerates of nanodiamonds were ensured. The homogeneous dispersion of nanodiamonds and their adhering role at fiber/matrix interface improved the mechanical properties of the composites. The developed composites are ideal candidate materials for engineering applications demanding high specific mechanical properties.