Pervaporation Membranes for Seawater Desalination Based on Geo–rGO–TiO2 Nanocomposites. Part 1: Microstructure Properties

This is the first of two papers about the synthesis and microstructure properties of the Geo–rGO–TiO2 ternary nanocomposite, which was designed to suit the criteria of a pervaporation membrane for seawater desalination. The performance and capability of Geo–rGO–TiO2 as a seawater desalination pervaporation membrane are described in the second paper. A geopolymer made from alkali-activated metakaolin was utilized as a binder for the rGO-TiO2 nanocomposite. A modified Hummer’s method was used to synthesize graphene oxide (GO), and a hydrothermal procedure on GO produced reduced graphene oxide (rGO). The adopted approach yielded high-quality GO and rGO, based on Raman spectra results. The nanolayered structure of GO and rGO is revealed by Transmission Electron Microscopy (TEM) images. The Geo–rGO–TiO2 ternary nanocomposite was created by dispersing rGO nanosheets and TiO2 nanoparticles into geopolymer paste and stirring it for several minutes. The mixture was then cured in a sealed mold at 70 °C for one hour. After being demolded, the materials were kept for 28 days before being characterized. Fourier Transform Infrared (FTIR) and X-ray Diffraction (XRD) measurements revealed that the geopolymer matrix efficiently bonded the rGO and TiO2, creating nanocomposites. Scanning Electron Microscopy (SEM) coupled with Energy Dispersive Spectroscopy (EDS) was used to examine the morphology of the outer layer and cross-sections of nanocomposites, and the results displayed that rGO were stacked on the surface as well as in the bulk of the geopolymer and will potentially function as nanochannels with a width of around 0.36 nm, while TiO2 NPs covered the majority of the geopolymer matrix, assisting in anti-biofouling of the membranes. The pores structure of the Geo–rGO–TiO2 were classified as micro–meso pores using the Brunauer–Emmet–Teller (BET) method, indicating that they are appropriate for use as pervaporation membranes. The mechanical strength of the membranes was found to be adequate to withstand high water pressure during the pervaporation process. The addition of rGO and TiO2 NPs was found to improve the hyropobicity of the Geo–rGO–TiO2 nanocomposite, preventing excessive seawater penetration into the membrane during the pervaporation process. The results of this study elucidate that the Geo–rGO–TiO2 nanocomposite has a lot of potential for application as a pervaporation membrane for seawater desalination because all of the initial components are widely available and inexpensive.

A Theoretical Analysis on a Multi-Bed Pervaporation Membrane Reactor during Levulinic Acid Esterification Using the Computational Fluid Dynamic Method

Pervaporation is a peculiar membrane separation process, which is considered for integration with a variety of reactions in promising new applications. Pervaporation membrane reactors have some specific uses in sustainable chemistry, such as the esterification processes. This theoretical study based on the computational fluid dynamics method aims to evaluate the performance of a multi-bed pervaporation membrane reactor (including poly (vinyl alcohol) membrane) to produce ethyl levulinate as a significant fuel additive, coming from the esterification of levulinic acid. For comparison, an equivalent multi-bed traditional reactor is also studied at the same operating conditions of the aforementioned pervaporation membrane reactor. A computational fluid dynamics model was developed and validated by experimental literature data. The effects of reaction temperature, catalyst loading, feed molar ratio, and feed flow rate on the reactor’s performance in terms of levulinic acid conversion and water removal were hence studied. The simulations indicated that the multi-bed pervaporation membrane reactor results to be the best solution over the multi-bed traditional reactor, presenting the best simulation results at 343 K, 2 bar, catalyst loading 8.6 g, feed flow rate 7 mm3/s, and feed molar ratio 3 with levulinic acid conversion equal to 95.3% and 91.1% water removal.

Organophosphorus Polyurethane Ionomers as Water Vapor Permeable and Pervaporation Membranes

Organophosphorus polyurethane ionomers (AEPA-PU) based on aminoethers of ortho-phosphoric acid (AEPA) were obtained and studied as pervaporation membrane materials for separating isopropanol/water mixtures. The regularities of the change in the water vapor permeability of AEPA-PU were also investigated. It has been established that an increase of solute content in the composition of the urethane-forming system and the content of ionogenic groups in AEPA leads to a noticeable increase in the vapor permeability of the resulting film materials. An increase in water vapor permeability values is accompanied by a significant increase in the pervaporation characteristics of AEPU-PU. It was shown that the conditions promoting clustering of phosphate anions cause an increase in the values of the vapor permeability coefficient of AEPA-PU obtained using polyoxypropylene glycol. However, the hydrophobicity of the polypropylene glycol surrounding the clusters makes it difficult for water to move through the polymer matrix. Due to the hydrophilicity of polyoxyethylene glycol, the highest values of water vapor permeability and pervaporation characteristics are achieved for AEPA-PU synthesized using PEG.