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Abstract: A new type of forward osmosis (FO) hollow fiber membranes with an antifouling nanofiltration (NF)-like selective layer has been developed in this work. The fabrication involves a step of porous poly(amide-imide) (PAI) ultrafiltration (UF) hollow fiber spinning via phase inversion, followed by simple polyelectrolyte post-treatments using positively charged polyethyleneimine (PEI) for cross-linking and negatively charged polystyrene sulfonate sodium salt (PSS) for deposition. The membranes are subsequently characterized by a series of standard protocols and evaluated in FO process. The PAI FO membranes possess a pure water permeability of 3.7–4.3Lm−2 h−1 bar−1 and Na2SO4 rejections up to 85% at 1bar. In the FO process, the membranes can achieve water flux of 17 and 12Lm−2 h−1 for active layer facing draw solution (AL-facing-DS) and active layer facing feed water (AL-facing-FW) configurations, respectively, using a 2000ppm Na2SO4 aqueous solution as the feed and 0.5M Na2SO4 as the draw solution. When the feed contained 1000ppm bovine serum albumin (BSA) and 2000ppm Na2SO4, a steady water flux of 11Lm−2 h−1 can be maintained using 0.5M Na2SO4 as the draw solution at ambient temperature of 23°C. The approach of making FO membranes developed in the present study offers the advantages of simple fabrication process, tailorable selective layer and promising membrane performance for protein-contained wastewater treatment by FO process. [Copyright &y& Elsevier]

Abstract: Hollow fiber membranes with a positively charged nanofiltration (NF)-like selective layer have been successfully fabricated by utilizing asymmetric microporous hollow fibers made of Torlon® polyamide–imide (PAI) material as the porous substrate followed by polyelectrolyte post-treatment using polyethyleneimine (PEI), which has not been reported previously. The reaction between PAI and PEI has been confirmed by experiments. The membrane structure and surface property are carefully tailored by adjusting polymer dope composition, spinning conditions and the post-treatment parameters. These membranes are, subsequently, characterized by a series of standard protocols in terms of membrane morphology, structure, permeability and salt rejection, and are applied in forward osmosis (FO) processes. The newly developed PAI hollow fiber membranes show a pure water permeability of 2.19–2.25L/m2 hbar and reasonable NaCl and MgCl2 rejections of 49% and 94% at 1bar, respectively. It is also found that in FO processes, when using 0.5M MgCl2 as a draw solution and DI water as the feed in the active layer facing feed water (AL-facing-FW) configuration at 23°C, the water fluxes of two PAI FO hollow fiber membranes are 8.36 and 9.74L/m2 h, respectively, and the J S /J V of the two membranes is smaller than 0.4g/L, which is lower than the data of 0.85g/L for commercial FO membrane from Hydration Technologies Inc. (HTI). Different from a neutral membrane, the positively charged FO membrane provides double electric repulsions to the salt transfer through the membrane in the AL-facing-FW configuration, leading to a reduction of salt penetration, while in the active layer facing draw solution (AL-facing-DS) configuration, the positive charges facilitate salt transportation. This study provides a simple and effective approach to make hollow fibers suitable for FO applications. [Copyright &y& Elsevier]

In this study, the glutaraldehyde (GA) crosslinking was adopted in combination of layer-by-layer (LBL) polyelectrolyte deposition to develop a novel hollow fiber NF membrane with low-pressure water softening capability for synthesized hard water containing divalent counterion SO 4 2− . The challenges for the new membrane include (a) the presence of SO 4 2− in the feed water, which tends to deteriorate positively charged NF membrane retention to divalent ions; (b) high salinity feed water up to 10,000 ppm total dissolved salt (TDS); (c) 2 bar operating pressure that requires the membrane to have a good Mg 2+ /Na + selectivity and less mass transfer resistance in the substrate; and (d) better separation performance as compared with the state-of-the-art and commercial NF membranes. Based on the membrane characterization results, the possible structure of the deposited layers and the effect of GA crosslink was proposed. It was found that the crosslinking could tighten the membrane surface pores with increased hydrophilicity while the membrane surface charge was reduced. Therefore, mainly based on the size exclusion, the crosslinked LBL*1.5C membrane showed more than 10 LMH/bar permeability with above 95% rejection to each of 1000 ppm MgCl 2 , MgSO 4 and Na 2 SO 4 solution under 2 bar pressure. It was also proved to be more suitable for the low-pressure water softening application at 2 bar in all tested feed water with the presence of SO 4 2− and TDS up to 10,000 ppm in terms of both permeability and hardness removal efficiency when compared with commercial NF 270 and NF 90 membranes. [ABSTRACT FROM AUTHOR]

The layer-by-layer (LBL) polyelectrolyte deposited membranes have drawn increasing attention in various applications due to the ease of selective layer formation and their stability and versatility. In this study, the LBL deposition was performed at the inner surface of the polyethersulfone (PES) hollow fiber substrate to form composite nanofiltration (NF) membrane. The semi-dynamic deposition procedure was adopted with the aid of syringes. The newly developed inner deposited (id-LBL) membranes were then tested in NF and forward osmosis (FO) applications and the performance were compared with outer surface deposition as well as some literature data. The id-LBL membranes could not only withstand higher operating pressure but also possess superior hardness rejection especially in high concentration mixed salt solutions (more than 95% rejection to Mg 2+ and Ca 2+ in a 5000 ppm total dissolved salt (TDS) mixture under 4.8 bar). As for the FO process, with only two layer deposition, the id-LBL membranes also demonstrated significant performance improvement with increased water flux (up to 70 L/m 2 h using 0.5 M MgCl 2 as draw solution in active layer facing draw solution configuration) and reduced salt leakage (around 0.5 g/m 2 h using 1 M MgCl 2 draw solution in active layer facing feed water configuration). This study suggests that for hollow fiber substrate, the inner surface is more suitable for the formation of the selective layer via LBL deposition than the outer surface. [ABSTRACT FROM AUTHOR]

The use of nanotechnology in water separation membranes is a promising approach to alleviate the global water crisis. Graphene oxide (GO) with its unique water transport property has exhibited high potential for application in the water treatment processes. In this study, we have designed and fabricated a novel nanofiltration (NF)-like GO surface deposited poly(amide-imide)–polyethyleneimine (PAI–PEI) hollow fiber membrane. The PAI hollow fiber substrate was prepared by phase inversion and modified with PEI to obtain a positively charged membrane surface. The negatively charged GO nanosheets were then electrostatically immobilized onto the membrane surface via an instant dip-coating to form the NF-like selective layer. Our results have shown that the GO nanosheets serve as effective selective barriers and can achieve higher water permeability up to 86% without compromising membrane selectivity when used to substitute part of the PEI cross-linked selective layer. This is attributed to the smaller hydrodynamic resistance of GO nanosheets and their ability to effectively narrow the pore size distribution. Moreover, shortening of the membrane modification time and better mechanical properties of the GO modified membrane can be attained by avoiding excessive PEI cross-linking. The GO deposition also exhibits good stability when subjected to a backwashing pressure of 100,000 Pa and a cross-flow rate of 600 mL/min, which corresponds to a velocity of 14 cm/s and a Reynolds number of ~870. These results have demonstrated a high potential of using this GO modified hollow fiber membrane for large scale water softening applications. [ABSTRACT FROM AUTHOR]

Abstract: The layer-by-layer (LBL) polyelectrolyte deposition was applied on polyethersulfone (PES) hollow fiber ultrafiltration membrane to prepare nanofiltration (NF) membrane for low pressure water softening application for the first time. The effects of polyelectrolyte type and molecular weight (MW), deposited bilayer number, polyelectrolyte solution pH and supporting electrolyte concentration on the performance of resultant membranes were studied thoroughly. Experiments revealed that the pH of the polyelectrolyte solution and supporting electrolyte concentration presented the most notable effects. For weak poly-cations, Poly(ethylenimine) (PEI) and Poly(allylamine hydrochloride) (PAH), the solution pH affected the membrane performance significantly, and high water permeability and divalent cation rejection were obtained at optimum pH values. Using a low concentration of supporting electrolyte at underneath layers was proved to be an effective way to increase water permeability while maintaining high salt rejection. A salt water flux (SWP) of 12LMH/bar and 94% Mg2+ rejection was obtained by depositing only two bilayers of PSS/PAH polyelectrolytes on the PES substrate, while for the 3000ppm mixed salt solution, the water permeability was 11LMH/bar with Mg2+ and Ca2+ rejection as high as 90%. These promising results demonstrate that LBL technique is potentially applicable for preparing low-pressure water softening hollow fiber membranes. [Copyright &y& Elsevier]