A Novel Approach To Optimize the Fabrication Conditions of Thin Film Composite RO Membranes Using Multi-Objective Genetic Algorithm II.

This work focuses on developing a novel method to optimize the fabrication conditions of polyamide (PA) thin film composite (TFC) membranes using the multi-objective genetic algorithm II (MOGA-II) method. We used different fabrication conditions for formation of polyamide layer-trimesoyl chloride (TMC) concentration, reaction time (t), and curing temperature (Tc)-at different levels, and designed the experiment using the factorial design method. Three functions (polynomial, neural network, and radial basis) were used to generate the response surface model (RSM). The results showed that the radial basis predicted good results (R2 = 1) and was selected to generate the RSM that was used as the solver for MOGA-II. The experimental results indicate that TMC concentration and t have the highest influence on water flux, while NaCl rejection is mainly affected by the TMC concentration, t, and Tc. Moreover, the TMC concentration controls the density of the PA, whereas t confers the PA layer thickness. In the optimization run, MOGA-II was used to determine optimal parametric conditions for maximizing water flux and NaCl rejection with constraints on the maximum acceptable levels of Na2SO4, MgSO4, and MgCl2 rejections. The optimized solutions were obtained for longer t, higher Tc, and different TMC concentration levels.

Novel route for amine grafting to chitosan electrospun nanofibers membrane for the removal of copper and lead ions from aqueous medium.

A novel step wise synthetic route was developed to prepare amine grafted nanofibers (AGNFs) affinity membrane. The chemical structure of the nanofibers (NFs) after grafting was studied by acquiring Fourier Transform Infrared (FT-IR) spectra and Carbon, Hydrogen and Nitrogen (CHN) data. The morphology of the NFs before and after grafting was studied by Field Emission Scanning Electron Microscope (FE-SEM). FT-IR and CHN data confirmed the introduction of new functional groups into the primary structure of chitosan (CH). FE-SEM showed denser membrane with no deterioration of the NFs morphology after grafting. The aqueous stability of the membranes was studied in distilled water. The AGNFs membranes showed good aqueous stabilities (with only ∼ 6% loss in weight until 24 h and remained stable thereafter) which was less than the weight loss by glutaraldehyde treated nanofibers (GNFs) (∼44% loss in weight until 24 h) and pristine NFs (100% loss in weight as soon as the NFs were immersed in distilled water). The maximum adsorption (qm) capacity of AGNFs for Cu (II) and Pb (II) was observed to be 166.67 mg.g-1 and 94.34 mg.g-1. The adsorption capacity of the present systems was much higher for Cu (II) when compared to the already existing conventional and chitosan adsorbents. This increased might be related not just to the size, but more potentially to the increase in the number of nitrogen binding sites (chelating sites). Nitrogen donates lone-pair of electrons for chelation. The combination of processing into nano size and amine grafting (AG) has significantly increased the adsorption capacity of CH NFs membrane.

Active removal of waste dye pollutants using Ta3N5/W18O49 nanocomposite fibres.

A scalable solvothermal technique is reported for the synthesis of a photocatalytic composite material consisting of orthorhombic Ta3N5 nanoparticles and WOx≤3 nanowires. Through X-ray diffraction and X-ray photoelectron spectroscopy, the as-grown tungsten(VI) sub-oxide was identified as monoclinic W18O49. The composite material catalysed the degradation of Rhodamine B at over double the rate of the Ta3N5 nanoparticles alone under illumination by white light, and continued to exhibit superior catalytic properties following recycling of the catalysts. Moreover, strong molecular adsorption of the dye to the W18O49 component of the composite resulted in near-complete decolourisation of the solution prior to light exposure. The radical species involved within the photocatalytic mechanisms were also explored through use of scavenger reagents. Our research demonstrates the exciting potential of this novel photocatalyst for the degradation of organic contaminants, and to the authors' knowledge the material has not been investigated previously. In addition, the simplicity of the synthesis process indicates that the material is a viable candidate for the scale-up and removal of dye pollutants on a wider scale.