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Abstract: Delamination-free ultrafiltration (UF) dual layer hollow fibers have been successfully fabricated by dry jet-wet spinning technique. Two different polymers of poly(amide-imide) (PAI) and polyethersulfone (PES) were utilized as the selective layer on the outer side and the porous support layer on the inner side, respectively. The dual layer substrates were subsequently modified to develop a nanofiltration (NF)-like skin on the outer layer by polyethyleneimine (PEI) cross-linking followed by multilayer polyelectrolyte depositions. These membranes were characterized by a series of standard protocols in terms of membrane structure, permeability and salt rejection, and were applied in FO process. Experiments reveal that the dual-layer NF hollow fiber modified by polyelectrolyte cross-linking and depositions can achieve pure water permeability of 4.1l/m2.h.bar and a high rejection to MgCl2 up to 97%. In FO process, the dual-layer hollow fibers exhibited a water flux of 39 and 21lm−2 h−1 in the orientations of active layer facing draw solution and feed water, respectively, by using 0.5M MgCl2 as draw solution and de-ionized (DI) water as feed at room temperature. It suggests that the combined treatment of polyelectrolyte cross-linking and deposition is an effective way to form a NF-like selective layer for FO dual-layer hollow fiber membranes. [Copyright &y& Elsevier]

One of the critical challenges faced by forward osmosis (FO) is the internal concentration polarization (ICP) during FO process, which can drastically reduce the effective osmotic driving force. In this work, silica nanoparticles were embedded in polyetherimide (PEI) nanofibrous support for making thin film nanocomposite (TFN) polyamide FO membranes to mitigate undesired ICP. The experimental results show that the pore size and porosity of the FO membrane substrate was significantly increased due to silica incorporation; the reason could be mainly attributed to the better heat-press resistance of the silica based nanofibrous substrates, leading to less substrate compaction and porosity reduction during the heat-press treatment. The FO membranes supported with such substrates demonstrated higher osmotic water flux, likely arising from the reduced structural parameter of the support layer. The current work showed that the FO membrane with the highest silica loading of 1.6 wt% in dope solution had the maximum substrate porosity (83%), the smallest structural parameter (~ 174 μm), and the most promising water flux, i.e., 42 L/m 2 h in the active layer facing the feed water orientation and 72 L/m 2 h in the active layer facing the draw solution orientation when 1.0 M NaCl draw solution and deionised feed water were applied. [ABSTRACT FROM AUTHOR]

One of the big challenges for forward osmosis (FO) practical application is the lack of high performance FO membranes. In this research, we successfully fabricated a novel thin film nanocomposite (TFN) FO membrane consisting of a polyetherimide (PEI) nanofibrous substrate reinforced by functionalized multi-walled carbon nanotubes (f-CNTs) and an ultrathin polyamide rejection layer. In addition to the superior inter-connected porous structure of nanofibrous substrate, the well-distributed f-CNTs in the nanofibers increased the substrate porosity by 18% and reduced membrane's structural parameter ( S value) by 30%, and significantly improved the substrate tensile modulus by 53%. The high mechanical strength provided by the embedded f-CNTs enabled us to further increase the substrate pore size and porosity in order to mitigate the internal concentration polarization (ICP). This was demonstrated by the high performance TFN-2 FO membrane with a structural parameter of 310 μm. Its water flux at 1.0 M NaCl draw solution (DS) was as high as 61 and 33 L/m 2 h in the active layer facing draw solution (AL-DS) and active layer facing feed water (AL-FW) orientations, respectively, indicating the success of the design strategy, i.e., improved membrane mechanical strength enables a further improvement of the membrane structure to mitigate the ICP. [ABSTRACT FROM AUTHOR]

Abstract: High performance flat sheet forward osmosis (FO) membranes have been successfully fabricated using Torlon® polyamide-imide (PAI) materials via phase inversion followed by polyelectrolyte polyethyleneimine (PEI) post-treatment to form a nanofiltration (NF)-like rejection layer with positive charges. The structure and charge property of the FO membranes were carefully tailored by optimizing casting conditions and selecting different immersing methods for the post-treatment. Especially, when the PAI micro-porous substrate was embedded with a woven fabric, the enhanced mechanical strength of the membrane made it possible to reduce the thickness of the substrate to 55μm, which is in favor of high water flux. The resultant membranes can reach a water flux of 29.65Lm−2 h−1 with a ratio of salt flux to water flux (J s /J v ) of <0.8gL−1 in the active layer facing draw solution (AL-facing-DS) configuration, or the water flux of 19.2Lm−2 h−1 and the J s /J v of <0.5gL−1 in the active layer facing feed water (AL-facing-FW) configuration using 0.5M MgCl2 as the draw solution and de-ionized water as the feed water at room temperature. [Copyright &y& Elsevier]

Forward osmosis (FO) is an increasingly important technology that has been deemed promising for addressing the global issue of water scarcity. Rapid progress over the past decade has been marked by significant innovations in the membrane development and process design. The key idea is to develop next-generation membranes through advanced membrane fabrication methods as well as hybrid systems where the FO process can really value-add. As such, this article provides an overview of the various FO membrane designs, in particular, the thin-film composite, surface-modified, and mixed matrix and biomimetic membranes. The pros and cons of each type of membranes are discussed together with the strategies used to optimize membrane properties such as structural parameter ( S ), water permeability ( A ) and salt permeability ( B ) to achieve enhanced FO performances. Furthermore, we also discuss the roles of FO in the various hybrid systems and evaluate the potential of these hybrid systems for desalination. Lastly, we provide our perspectives, especially in the area of membrane fabrications and FO hybrid systems, to shed light on the future research directions for harnessing the true potential of FO for desalination. [ABSTRACT FROM AUTHOR]

Internal concentration polarization (ICP) in a dense support layer is one of the main reasons holding back forward osmosis (FO) process. In this regard, a highly porous microstructured support (HPμS) featuring a quasi-sponge-free sublayer pore structure can be considered a suitable alternative to develop high-performance FO membranes. However, it has not been tested for its effects on FO. This study demonstrates that a TFC membrane prepared using the HPμS works out for FO by inducing 3.35 times higher water flux without compromising a reverse salt flux (J s) compared to a control TFC membrane prepared without support adjustment. The performance improvement could be achieved by HPμS's almost no sponge-like region and lateral walls, which were desirable to minimize ICP. Furthermore, we verified that it is possible to leverage co-solvent assisted interfacial polymerization (CAIP) to further improve FO membrane performances by creating a more permeable active layer. The in-house TFC membrane optimized by the HPμS and CAIP displayed 5.3 times higher FO water flux than the control membrane, while keeping comparable J s. We expect that this research could contribute to kicking the FO membrane performance up a notch by providing a practical example of simultaneous optimization of both support and active layers. [Display omitted] • A highly porous microstructured support (HPμS) successfully reduced ICP in FO. • Almost no sponge-like region and lateral walls of the HPμS were key in reducing ICP. • A sublayer structure of a support layer was examined by a non-destructive inspection. • Co-solvent assisted interfacial polymerization further improved FO performances. • The simultaneous optimizations of support and active layers maximized FO performances. [ABSTRACT FROM AUTHOR]

This paper presents studies on the interactions and effects of biomacromolecules compounds on forward osmosis (FO) membrane performance. Individual components and a combination of various organic substances such as bovine serum albumin (BSA), dextran, sodium alginate and xanthan gum were used as model feeds and tested for their influences on FO performance with the active layer of the FO hollow fiber membrane facing the feed solution (AL-FS). The interactions between foulants were examined by using fluorescence spectroscopy, rotational rheometry and laser doppler micro-electrophoresis techniques. For a system containing combined organic foulants, it was found that viscosity was not the dominant factor governing FO membrane fouling as the decrease in viscosity did not always result in less fouling. The effect of divalent cations on the FO fouling behavior was also studied by adding CaCl 2 . The presence of calcium ions has exacerbated the flux decline, this occurred particularly for any combined organic foulants containing alginate, due to intermolecular bridging among alginate molecules. It is interesting to note that combined BSA + alginate caused moderate flux decline, while BSA and alginate alone did not cause any observable water flux loss. The (BSA + alginate) fouling became more severe with the presence of calcium ions. [ABSTRACT FROM AUTHOR]

Produced water management is one of the key challenges faced by the oil and gas industry globally. Specifically, the gas industry in Qatar is challenged to minimize the produced/process water (PPW) volumes injected into disposal wells to ensure long term sustainability of the reservoirs. This research evaluated a novel application of forward osmosis (FO) to reduce the volumes of PPW disposed of by deep well injection using brine from thermal desalination plants or seawater as draw solutions. In the case of brines, this process also provides some environmentally beneficial dilution before discharge. In order to verify the PPW volume reduction concept, bench-scale FO experiments were carried out using commercial flat sheet membranes. FO performance was evaluated using PPW with and without pretreatment and results confirm that pretreatment is key to the successful implementation of FO for the treatment of PPW. Experimental results indicate that FO is effective in achieving 50% volume reduction of pretreated PPW with stable flux of 12 LMH. Lab analyses show that the TOC in the diluted draw solution was below the detection limit indicating that the TOC from the feed did not appear in the draw solution and hence would not be discharged to the environment. [ABSTRACT FROM AUTHOR]

In this paper, the viability of using micellar draw solutions (DS) for Forward Osmosis (FO) is presented for the first time. Above the critical micelle concentration (CMC) and the Krafft temperature (Tk), the monomers in a surfactant solution aggregate to form micelles, resulting in a relatively constant osmotic pressure above the CMC. These properties can be useful for a FO system in order to maintain a constant water flux and to enable draw solution regeneration at low energy. Three cationic and two anionic surfactants were studied at different concentrations as potential draw solutions for FO applications. Both flat sheet and hollow fiber FO membranes were used in the study. The study revealed that the micellar solutions generated more stable flux compared to other inorganic DS; the hypothesis of a constant flux above the CMC was valid only for concentrations slightly above the CMC, and micellar solutions behaved similar to inorganic solutes at concentrations significantly higher than the CMC. It was shown that external concentration polarization (ECP) does not have a significant effect in micellar solutions just above the CMC. Furthermore, all surfactants demonstrated between 3 and 300 times less reverse transport compared to NaCl at similar concentrations. Finally, the surfactant solute could be regenerated with recoveries as high as between 95% and 99%. It was thus verified that micellar solutions are an attractive DS for application to Forward Osmosis and potentially in the forward osmosis membrane bioreactor (FO-MBR). [ABSTRACT FROM AUTHOR]

Abstract: Great efforts from the membrane community have been devoted in developing suitable membranes for forward osmosis (FO) applications in recent years. In the current study, the layer-by-layer (LBL) polyelectrolyte assembly technique has been successfully applied onto a microporous polyethersulfone (PES) hollow fiber substrate to make novel LBL hollow fiber membranes suitable for FO process for the first time. The FO performance of the LBL hollow fibers with different numbers of deposited layers has been evaluated using deionized (DI) water as the feed and MgCl2 solution of various concentrations as the draw solution in both orientations. With 6 layers deposited and in the active layer facing draw solution (AL-facing-DS) orientation, the membrane showed high water fluxes of 14.6, 25.9 and 40.5L/m2 h with corresponding salt to water flux, J s /J v, ratio of 0.034, 0.066 and 0.201g/L using 0.05, 0.1 and 0.5M draw solution, respectively. These promising results demonstrate the potential application of the LBL hollow fibers in FO process using low concentration draw solutions, which can substantially reduce the draw solution replenishment, and the energy consumption for draw solution regeneration and separation. [Copyright &y& Elsevier]

Abstract: There has been an increasing interest in the novel integration of forward osmosis (FO) and biological process known as the osmotic membrane bioreactor (OMBR). However, little operating experience is available to adequately assess the feasibility of the technology for larger scale application. The goal of this study is to provide fundamental information on the technology. In this study, an OMBR system was continuously operated for 73days. It was found that the high retention property of the FO membrane and salt transmission from the draw solution resulted in increasing mixed liquor salinity until a stable state was reached. In spite of the elevated salinity, the water flux was relatively stable at around 3Lm−2 h−1. Post-experiment analyses indicated mild membrane fouling, and its effect on water permeability was insignificant. An ion analysis check indicated that scaling did not occur. The SEM examination detected a thin gel-like secondary layer on the membrane surface. It was deduced that this secondary layer could have an influencing role on salt transmission during the experiment, and moderated salt concentration in the bioreactor. [Copyright &y& Elsevier]