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Wetland water is an alternative water resource around wetland areas. However, it is typically saline due to seawater intrusion and contains high natural organic matter (NOM) that is challenging to treat. This study evaluated the stability of interlayer-free mesoporous silica matrix membranes employing a dual acid–base catalyzed sol–gel process for treatment of saline wetland water. The silica sols were prepared under a low silanol concentration, dip-coated in 4 layers, and calcined using the rapid thermal processing method. The membrane performance was initially evaluated through pervaporation under various temperatures (25–60 °C) using various feeds. Next, the long-term stability (up to 400 h) of wetland saline water desalination was evaluated. Results show that the water flux increased at higher temperatures up to 6.9 and 6.5 kg·m−2·h−1 at the highest temperature of 60 °C for the seawater and the wetland saline water feeds, respectively. The long-term stability demonstrated a stable performance without flux and rejection decline up to 170 h operation, beyond which slow declines in water flux and rejection were observed due to fouling by NOM and membrane wetting. The overall findings suggest that an interlayer-free mesoporous silica membrane offers excellent performance and high salt rejection (80–99%) for wetland saline water treatments. [ABSTRACT FROM AUTHOR]

This work shows the preparation of silica membranes by a two-step sol-gel method using tetraethyl orthosilicate in ethanolic solution by employing nitric acid and ammonia as co-catalysts. The sols prepared in pH 6 resulted in the lowest concentration of silanol (Si-OH) species to improve hydrostability and the optimized conditions for film coating. The membrane was tested to desalinate 0.3-15 wt % synthetic sodium chloride (NaCl) solutions at a feed temperature of 22 °C followed by long term membrane performance of up to 250 h in 3.5 wt % NaCl solution. Results show that the water flux (and salt rejection) decrease with increasing salt concentration delivering an average value of 9.5 kg m-2 h-1 (99.6%) and 1.55 kg m-2 h-1 (89.2%) from the 0.3 and 15 wt % saline feed solutions, respectively. Furthermore, the permeate salt concentration was measured to be less than 600 ppm for testing conditions up to 5 wt % saline feed solutions, achieving below the recommended standard for potable water. Long term stability shows that the membrane performance in water flux was stable for up to 150 h, and slightly reduced from thereon, possibly due to the blockage of large hydrated ions in the micropore constrictions of the silica matrix. However, the integrity of the silica matrix was not affected by the long term testing as excellent salt rejection of >99% was maintained for over 250 h. [ABSTRACT FROM AUTHOR]

The high content of natural organic matter (NOM) is one of the challenging characteristics of peat water. It is also highly contaminated and contributes to some water-borne diseases. Before being used for potable purposes, peat water must undergo a series of treatments, particularly for NOM removal. This study investigated the effect of coagulation using aluminum sulfate coagulant and adsorption using powdered activated carbon (PAC) as a pretreatment of ultrafiltration (UF) for removal of NOM from actual peat water. After preparation and characterization of polysulfone (Psf)-based membrane, the system's performance was evaluated using actual peat water, particularly on NOM removal and the UF performances. The coagulation and adsorption tests were done under variable dosings. Results show that pretreatment through coagulation–adsorption successfully removed most of the NOM. As such, the UF fouling propensity of the pretreated peat water was substantially lowered. The optimum aluminum sulfate dosing of 175 mg/L as the first pretreatment stage removed up to 75–78% NOM. Further treatment using the PAC-based adsorption process further increased 92–96% NOM removals at an optimum PAC dosing of 120 mg/L. The final UF-PSf treatment reached NOM removals of 95% with high filtration fluxes of up to 92.4 L/(m2.h). The combination of three treatment stages showed enhanced UF performance thanks to partial pre-removal of NOM that otherwise might cause severe membrane fouling. [ABSTRACT FROM AUTHOR]

A membrane adsorbent was successfully made from palm empty fruit bunches (PEFB), which was pyrolysed as physical activation. The effect of adding the impact of one-step catalyst (hydrochloric acid) and differences in the concentration on the characteristics and structure and deconvolution are investigated in this study. The results of the research have been successfully created and characterised using Fourier-Transform Infrared (FTIR), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) isotherm, and membrane morphology using SEM test. Membrane performance testing was carried out using a biogas flame test. The adsorber membrane was made by adding NH4Cl as a cationic surfactant, polyvinyl acetate (PVA), and polyethylene glycol (PEG) with a ratio of 1:3. The FTIR test has a functional group: O-H; C-H stretch; C=C-C; Arly O-Strech; C-O. Adsorbent membrane with the addition of 0.5 M HCl catalyst had the highest ratio of O-H/C=C-C relative area of 4.33. The diffractogram shows an amorphous structure with (002) and (100) graph planes. Adsorber membrane with a concentration of 1.5 M HCl has formed amorphous structured fibre. The adsorber membrane with a concentration of 0.5 HCl activator gave a surface area of 0.5345 m2 g−1 and a pore volume of 0.000983 cm3 g−1. [ABSTRACT FROM AUTHOR]

This review provides a global overview of microporous silica based membranes for desalination via pervaporation with a focus on membrane synthesis and processing, transport mechanisms and current state of the art membrane performance. Most importantly, the recent development and novel concepts for improving the hydro-stability and separating performance of silica membranes for desalination are critically examined. Research into silica based membranes for desalination has focussed on three primary methods for improving the hydro-stability. These include incorporating carbon templates into the microporous silica both as surfactants and hybrid organic-inorganic structures and incorporation of metal oxide nanoparticles into the silica matrix. The literature examined identified that only metal oxide silica membranes have demonstrated high salt rejections under a variety of feed concentrations, reasonable fluxes and unaltered performance over long-term operation. As this is an embryonic field of research several target areas for researchers were discussed including further improvement of the membrane materials, but also regarding the necessity of integrating waste or solar heat sources into the final process design to ensure cost competitiveness with conventional reverse osmosis processes. [ABSTRACT FROM AUTHOR]

The physicochemical properties of organo-silica xerogels derived from organo catalyst were pervasively investigated, including the effect of one-step catalyst (citric acid) and two-step catalyst (acid-base), and also to observe the effect of sol pH of organo-silica xerogel toward the structure and deconvolution characteristic. The organo-silica xerogels were characterized by FTIR, TGA and nitrogen sorption to obtain the physicochemical properties. The silica sol–gel method was applied to processed materials by employing TEOS (tetraethyl orthosilicate) as the main precursor. The final molar ratio of organo-silica was 1:38:x:y:5 (TEOS:ethanol: citric acid: NH3:H2O) where x is citric acid concentration (0.1–10 × 10−2 M) and y is ammonia concentration (0 to 3 × 10−3 M). FTIR spectra shows that the one-step catalyst xerogel using citric acid was handing over the higher Si-O-Si concentration as well as Si-C bonding than the dual catalyst xerogels with the presence of a base catalyst. The results exhibited that the highest relative area ratio of silanol/siloxane were 0.2972 and 0.1262 for organo catalyst loading at pH 6 and 6.5 of organo-silica sols, respectively. On the other hand, the organo-silica matrices in this work showed high surface area 546 m2 g−1 pH 6.5 (0.07 × 10−2 N citric acid) with pore size ~2.9 nm. It is concluded that the xerogels have mesoporous structures, which are effective for further application to separate NaCl in water desalination. [ABSTRACT FROM AUTHOR]

Water scarcity is still a pressing issue in many regions. The application of membrane technology through water desalination to convert brackish to potable water is a promising technology to solve this issue. This study compared the performance of templated TEOS-P123 and ES40-P123 hybrid membranes for brackish water desalination. The membranes were prepared by the sol–gel method by employing tetraethyl orthosilicate (TEOS) for the carbon-templated silica (soft template) and ethyl silicate (ES40) for the hybrid organo-silica. Both sols were templated by adding 35 wt.% of pluronic triblock copolymer (P123) as the carbon source. The silica-templated sols were dip-coated onto alumina support (four layers) and were calcined by using the RTP (rapid thermal processing) method. The prepared membranes were tested using pervaporation set up at room temperature (~25 °C) using brackish water (0.3 and 1 wt.%) as the feed. It was found that the hybrid membrane exhibited the highest specific surface area (6.72 m2·g−1), pore size (3.67 nm), and pore volume (0.45 cm3·g−1). The hybrid ES40-P123 was twice thicker (2 μm) than TEOS-P123-templated membranes (1 μm). Lastly, the hybrid ES40-P123 displayed highest water flux of 6.2 kg·m−2·h−1. Both membranes showed excellent robustness and salt rejections of >99%. [ABSTRACT FROM AUTHOR]