Pervaporation, mainly utilized to separate azeotropic mixtures, has been paid much attention for desalination in recent years due to its numerous advantages.
A TiO2@MWCNTs (multi-wall carbon nanotubes) nanocomposite photoanode is prepared for photoelectrochemical water splitting in this study. The physical and photoelectrochemical properties of the photoanode are characterized using field emission-scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and linear sweep voltammetry. The results show that the TiO2@MWCNTs nanocomposite has an optical bandgap of 2.5 eV, which is a significant improvement in visible-light absorption capability compared to TiO2 (3.14 eV). The cyclic voltammograms show that incorporating TiO2 with the MWCNTs leads to a decrease in the electrical double layer, thereby facilitating the electron transfer rate in the TiO2@MWCNTs electrode. Moreover, the current density of the photoelectrochemical electrode formed by TiO2@MWCNTs under solar irradiation is significantly higher than that prepared by TiO2 (vs Ag/AgCl). The low charge capacity of the TiO2@MWCNTs electrode–electrolyte interface hinders the recombination of the photogenerated electrons and holes, which contributes to the enhancement of the solar-to-hydrogen (STH) conversion efficiency. The average STH conversion efficiency of the TiO2@MWCNTs electrode under solar exposure from 6 AM to 5 PM is 11.1%, 8.88 times higher than that of a TiO2 electrode. The findings suggested TiO2@MWCNTs is a feasible nanomaterial to fabricate the photoanode using photoelectrochemical water splitting under solar irradiation.
These days, ethanol fuel has been widely consumed worldwide to replace gasoline due to its possible environmental and long-term economic advantages. In detail, the ethanol fuel (purity ≥ 99.5 wt%) has been produced by traditional separation processes such as azeotropic distillation or molecular sieve adsorption, which excessively employs energy and capital cost. The pervaporation has already been considered as an effective alternative to conventional methods because of its high separation efficiency and low power consumption. Pervaporation separation of ethanol/water solution using hydrophilic membranes has been extensively studied owing to their superior perm-selectivity. In this present work, the polyvinyl alcohol thin-film composite membrane is prepared by casting a thin crosslinked polyvinyl alcohol (PVA) film on the polyacrylonitrile (PAN) porous substrate. The effect of PVA concentration on the pervaporation performance of the fabricated membrane is studied. The physicochemical properties of the prepared membrane are characterized using FTIR, SEM images, and contact angle measurements. The separation performance in terms of permeation flux and selectivity is simultaneously evaluated through a pervaporation dehydration of ethanol/water mixture of 80/20 wt.% at 60°C. The results show that the increase in PVA concentration leads to the decline in the hydrophilicity and the growth of the thickness and swelling degree of the membrane. Therefore, the selectivity of the membrane is found to improve significantly, while the permeation flux decreased with the PVA concentration ranging from 2.5 to 15 wt.%. Based on the results, the PVA membrane prepared from the 10 wt.% concentration is likely to provide high separation performance.
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