Abstract:In this work we investigate the potential of a polyethylene glycol-polypropylene glycol-polyethylene glycol, tri-block copolymer as a template for a hybrid carbon/silica membrane for use in the non-osmotic desalination of seawater. Silica samples were loaded with varying amounts of tri-block copolymer and calcined in a vacuum to carbonize the template and trap it within the silica matrix. The resultant xerogels were analyzed with FTIR, Thermogravimetric analysis (TGA) and N2 sorption techniques, wherein it was… Show more
“…With increasing the carbon template (P123-20 and 35) concentration, the xerogels tended to form mesoporous materials with a higher adsorption saturation capacity above 0.35 p/p1 and a small degree of hysteresis. This results in an estimate of 25% increase in the surface area and pore volume with increasing P123 copolymer incorporation which is in good agreement with Ladewig et al [7] for similar sols, but prepared by the acid catalysed sol-gel method. Furthermore, when P123 concentration reached 50 wt%, it is clearly observed that the isotherm profiles are truly type IV isotherms and mesoporous as evidenced by their large extent of hysteresis near 0.5 p/p1 indicating the occurrence of capillary condensation.…”
Section: Resultssupporting
confidence: 87%
“…The high water fluxes coupled with consistent excellent salt rejections ( 499.5%) clearly indicate that the performance of the base catalysed silica membrane containing carbon moieties derived from P123 triblock copolymers is beyond the state of art. For instance, the water flux of 2.5 kg m À 2 h À 1 and salt rejections 4 99.8% of base catalysed P123-50 silica membranes at room temperature for a sea water with NaCl concentration of 3.5 wt% are comparable or even better than those reported in the literature for acid catalysed silica membranes prepared with hexadecyl trimethyl ammonium bromide surfactant (1.9 kg m À 2 h À 1 and 94%) [10], methyl tri-ethoxy silane and TEOS (1.7 kg m À 2 h À 1 and 95%) [8], triblock copolymer templated silica membranes (3.0 kg m À 2 h À 1 ; 97%) [7]. When compared to the performance of the cobalt oxide silica membranes [33], the water fluxes produced by the membranes in this work are at least 300% (P123-5) to 800% (P123-50) higher yet with similar salt rejections, irrespective of the feed salt concentration and temperature.…”
Section: Resultssupporting
confidence: 51%
“…In this process, the integrity of the silica membrane remained generally unaffected under water exposure, in particular inhibiting micropore collapse. Several groups modified carbon templated silica using Pluronics s triblock copolymers [7] and surfactants [8][9][10][11] as molecular sieving membranes in desalination. The organic templates were retained in the silica matrices as the membranes were calcined in inert nitrogen gas atmosphere.…”
“…With increasing the carbon template (P123-20 and 35) concentration, the xerogels tended to form mesoporous materials with a higher adsorption saturation capacity above 0.35 p/p1 and a small degree of hysteresis. This results in an estimate of 25% increase in the surface area and pore volume with increasing P123 copolymer incorporation which is in good agreement with Ladewig et al [7] for similar sols, but prepared by the acid catalysed sol-gel method. Furthermore, when P123 concentration reached 50 wt%, it is clearly observed that the isotherm profiles are truly type IV isotherms and mesoporous as evidenced by their large extent of hysteresis near 0.5 p/p1 indicating the occurrence of capillary condensation.…”
Section: Resultssupporting
confidence: 87%
“…The high water fluxes coupled with consistent excellent salt rejections ( 499.5%) clearly indicate that the performance of the base catalysed silica membrane containing carbon moieties derived from P123 triblock copolymers is beyond the state of art. For instance, the water flux of 2.5 kg m À 2 h À 1 and salt rejections 4 99.8% of base catalysed P123-50 silica membranes at room temperature for a sea water with NaCl concentration of 3.5 wt% are comparable or even better than those reported in the literature for acid catalysed silica membranes prepared with hexadecyl trimethyl ammonium bromide surfactant (1.9 kg m À 2 h À 1 and 94%) [10], methyl tri-ethoxy silane and TEOS (1.7 kg m À 2 h À 1 and 95%) [8], triblock copolymer templated silica membranes (3.0 kg m À 2 h À 1 ; 97%) [7]. When compared to the performance of the cobalt oxide silica membranes [33], the water fluxes produced by the membranes in this work are at least 300% (P123-5) to 800% (P123-50) higher yet with similar salt rejections, irrespective of the feed salt concentration and temperature.…”
Section: Resultssupporting
confidence: 51%
“…In this process, the integrity of the silica membrane remained generally unaffected under water exposure, in particular inhibiting micropore collapse. Several groups modified carbon templated silica using Pluronics s triblock copolymers [7] and surfactants [8][9][10][11] as molecular sieving membranes in desalination. The organic templates were retained in the silica matrices as the membranes were calcined in inert nitrogen gas atmosphere.…”
“…Therefore, as shown in this study that the carbon matrix offers the fine-tuning of porosity and pore volume, which are extremely important for determining water flux of the hollow fibers for water production as membranes. This is exemplified by numerous studies of microporous ceramic membranes for desalination [59][60][61] and alcohol pervaporation [62][63][64]. On the other hand, highly mesoporous membranes, although lead to a high water production, will fail to separate the solute from water due to pore-wetting effect [39,65].…”
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“…The experimental set-up included a feed vessel, peristaltic pump, membrane module, condenser unit, vacuum pump and data logging system connected to computer. 35 Despite the appearance of several smaller peaks and shoulders, the main exothermic peak at ~350 °C is sharp and narrow. The feed was introduced into membrane module at a flow rate of 5 L h -1 and circulated back into the feed vessel.…”
Section: Test Of Membrane Performance In Water Desalinationmentioning
A direct synthesis method is introduced to prepare mesoporous carbon-silica nanocomposite (CSN) membranes for water-treatment applications. Unlike the intricate and expensive nanocasting method, this triconstituent co-assembly method is a one-pot synthesis method using Pluronic F127 as templating agent with a hybrid organic-inorganic matrix formed by tetraethylorthosilicate (TEOS), resorcinol and formaldehyde. The silica content is varied in the polymer solution to investigate the material properties, stability of the nanocomposite mesostructured and membrane performance in vacuum membrane distillation (VMD). The CSN materials are carbonised under nitrogen at temperatures of 600-900 °C without any significant lattice shrinkage, demonstrating excellent stability. They possess a highly ordered pore structure with moderate BET surface area (430-550 m 2 g -1 ) and narrow pore size distribution at around 5.5-7.6 nm. Based on the FTIR and NMR analyses, there is no covalent bond between the carbon and silica networks, but the carbon compound was found to affect the condensation degree of the silica. Raising the temperature from 700 to 900 °C leads to further condensation of the carbon network, which in turn releases hydroxyl or water groups that can attack adjacent siloxane bonds. The CSN membranes performed well in VMD with water permeation flux up to 12 L m -2 h -1 and salt rejection > 99 %. This work shows that a different strategy of modifying silica-based membrane can be successfully applied for the desalination of saline waters through VMD.
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