28
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Mesoporous Silica Gel–Based Mixed Matrix Membranes for Improving Mass Transfer in Forward Osmosis: Effect of Pore Size of Filler

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The efficiency of forward osmosis (FO) process is generally limited by the internal concentration polarization (ICP) of solutes inside its porous substrate. In this study, mesoporous silica gel (SG) with nominal pore size ranging from 4–30 nm was used as fillers to prepare SG-based mixed matrix substrates. The resulting mixed matrix membranes had significantly reduced structural parameter and enhanced membrane water permeability as a result of the improved surface porosity of the substrates. An optimal filler pore size of ~9 nm was observed. This is in direct contrast to the case of thin film nanocomposite membranes, where microporous nanoparticle fillers are loaded to the membrane rejection layer and are designed in such a way that these fillers are able to retain solutes while allowing water to permeate through them. In the current study, the mesoporous fillers are designed as channels to both water and solute molecules. FO performance was enhanced at increasing filler pore size up to 9 nm due to the lower hydraulic resistance of the fillers. Nevertheless, further increasing filler pore size to 30 nm was accompanied with reduced FO efficiency, which can be attributed to the intrusion of polymer dope into the filler pores.

          Related collections

          Most cited references14

          • Record: found
          • Abstract: found
          • Article: not found

          Hierarchically ordered macro-mesoporous TiO₂-graphene composite films: improved mass transfer, reduced charge recombination, and their enhanced photocatalytic activities.

          Hierarchically ordered macro-mesoporous titania films have been produced through a confinement self-assembly method within the regular voids of a colloidal crystal with three-dimensional periodicity. Furthermore, graphene as an excellent electron-accepting and electron-transporting material has been incorporated into the hierarchically ordered macro-mesoporous titania frameworks by in situ reduction of graphene oxide added in the self-assembly system. Incorporation of interconnected macropores in mesoporous films improves the mass transport through the film, reduces the length of the mesopore channel, and increases the accessible surface area of the thin film, whereas the introduction of graphene effectively suppresses the charge recombination. Therefore, the significant enhancement of photocatalytic activity for degrading the methyl blue has been achieved. The apparent rate constants for macro-mesoporous titania films without and with graphene are up to 0.045 and 0.071 min(-1), respectively, almost 11 and 17 times higher than that for pure mesoporous titania films (0.0041 min(-1)).
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Forward osmosis for application in wastewater treatment: a review.

            Research in the field of Forward Osmosis (FO) membrane technology has grown significantly over the last 10 years, but its application in the scope of wastewater treatment has been slower. Drinking water is becoming an increasingly marginal resource. Substituting drinking water for alternate water sources, specifically for use in industrial processes, may alleviate the global water stress. FO has the potential to sustainably treat wastewater sources and produce high quality water. FO relies on the osmotic pressure difference across the membrane to extract clean water from the feed, however the FO step is still mostly perceived as a "pre-treatment" process. To prompt FO-wastewater feasibility, the focus lies with new membrane developments, draw solutions to enhance wastewater treatment and energy recovery, and operating conditions. Optimisation of these parameters are essential to mitigate fouling, decrease concentration polarisation and increase FO performance; issues all closely related to one another. This review attempts to define the steps still required for FO to reach full-scale potential in wastewater treatment and water reclamation by discussing current novelties, bottlenecks and future perspectives of FO technology in the wastewater sector.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Influence of zeolite crystal size on zeolite-polyamide thin film nanocomposite membranes.

              Zeolite-polyamide thin film nanocomposite membranes were coated onto polysulfone ultrafiltration membranes by interfacial polymerization of amine and acid chloride monomers in the presence of Linde type A zeolite nanocrystals. A matrix of three different interfacial polymerization chemistries and three different-sized zeolite crystals produced nanocomposite thin films with widely varying structure, morphology, charge, hydrophilicity, and separation performance (evaluated as reverse osmosis membranes). Pure polyamide film properties were tuned by changing polymerization chemistry, but addition of zeolite nanoparticles produced even greater changes in separation performance, surface chemistry, and film morphology. For fixed polymer chemistry, addition of zeolite nanoparticles formed more permeable, negatively charged, and thicker polyamide films. Smaller zeolites produced greater permeability enhancements, but larger zeolites produced more favorable surface properties; hence, nanoparticle size may be considered an additional "degree of freedom" in designing thin film nanocomposite reverse osmosis membranes. The data presented offer additional support for the hypothesis that zeolite crystals alter polyamide thin film structure when they are present during the interfacial polymerization reaction.
                Bookmark

                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                23 November 2015
                2015
                : 5
                : 16808
                Affiliations
                [1 ]Key Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM), Jiangsu National Synergistic Innovation Center for Advanced Materials (SICAM), Institute of Advanced Materials, Nanjing Tech University (NanjingTech) , Nanjing 211816, P. R. China
                [2 ]Nanyang Environment & Water Research Institute, Interdisciplinary Graduate School, Nanyang Technological University , Singapore, 639798
                [3 ]Singapore Membrane Technology Centre, Nanyang Environment & Water Research Institute, Nanyang Technological University , Singapore, 637141
                [4 ]Department of Civil Engineering, the University of Hong Kong , Pokfulam, Hong Kong.
                Author notes
                [*]

                These authors contributed equally to this work.

                Article
                srep16808
                10.1038/srep16808
                4655366
                26592565
                542f04f7-762f-44c6-a738-bad3631c513a
                Copyright © 2015, Macmillan Publishers Limited

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 10 December 2014
                : 10 March 2015
                Categories
                Article

                Uncategorized
                Uncategorized

                Comments

                Comment on this article