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      Propylene/propane permeation properties of ethyl cellulose (EC) mixed matrix membranes fabricated by incorporation of nanoporous graphene nanosheets

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          Abstract

          Nanopore containing graphene nanosheets were synthesized by graphene oxide and a reducing agent using a facile hydrothermal treatment in sodium hydroxide media. The as-prepared nanoporous graphene was incorporated into ethyl cellulose (EC) to prepare the mixed matrix membranes (MMMs) for C 3H 6/C 3H 8 separation. Transmission electron microscopy (TEM) photograph and X-ray photoelectron spectroscopy (XPS) analysis of nanoporous graphene nanosheets indicated that the structure of nano-pore was irregular and the oxygen-containing groups in the surface were limited. More importantly, the as-prepared MMMs presented better separation performance than that of pristine EC membrane due to simultaneous enhancement of C 3H 6 permeability and ideal selectivity. The ideal selectivity of the MMMs with 1.125 wt‰ nanoporous graphene content for C 3H 6/C 3H 8 increased from 3.45 to 10.42 and the permeability of C 3H 6 increased from 57.9 Barrer to 89.95 Barrer as compared with the pristine membrane. The presumed facilitated mechanism was that the high specific surface area of nanoporous graphene in polymer matrix increased the length of the tortuous pathway formed by nanopores for the gas diffusion as compared with the pristine graphene nanosheets, and generated a rigidified interface between the EC chains and fillers, thus enhanced the diffusivity selectivity. Therefore, it is expected that nanoporous graphene would be effective material for the C 3H 6/C 3H 8 separation.

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          Impermeable Atomic Membranes from Graphene Sheets

          We demonstrate that a monolayer graphene membrane is impermeable to standard gases including helium. By applying a pressure difference across the membrane, we measure both the elastic constants and the mass of a single layer of graphene. This pressurized graphene membrane is the world's thinnest balloon and provides a unique separation barrier between 2 distinct regions that is only one atom thick.
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            Polymer nanosieve membranes for CO2-capture applications.

            Microporous organic polymers (MOPs) are of potential significance for gas storage, gas separation and low-dielectric applications. Among many approaches for obtaining such materials, solution-processable MOPs derived from rigid and contorted macromolecular structures are promising because of their excellent mass transport and mass exchange capability. Here we show a class of amorphous MOP, prepared by [2+3] cycloaddition modification of a polymer containing an aromatic nitrile group with an azide compound, showing super-permeable characteristics and outstanding CO(2) separation performance, even under polymer plasticization conditions such as CO(2)/light gas mixtures. This unprecedented result arises from the introduction of tetrazole groups into highly microporous polymeric frameworks, leading to more favourable CO(2) sorption with superior affinity in gas mixtures, and selective CO(2) transport by presorbed CO(2) molecules that limit access by other light gas molecules. This strategy provides a direction in the design of MOP membrane materials for economic CO(2) capture processes.
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              Tailoring assembly of reduced graphene oxide nanosheets to control gas barrier properties of natural rubber nanocomposites.

              Self-assembling of reduced graphene oxide platelets, as a tailored interconnected network within a natural rubber matrix, is proposed as a mean for obtaining nanocomposites with improved gas barrier, as compared to neat natural rubber. Interestingly, this nanocomposite structure results to be much more effective than homogeneous dispersion of graphene platelike particles, even at low graphene loadings. Such behavior is interpreted on the grounds of a theoretical model describing permeability of heterogeneous systems specifically accounting for self-segregated graphene morphology.
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                29 June 2016
                2016
                : 6
                : 28509
                Affiliations
                [1 ]State Key Laboratory of Heavy Oil Processing, China University of Petroleum (East China) , Qingdao 266580, P.R. China
                [2 ]College of Science, China University of Petroleum (East China) , Qingdao 266580, P.R. China
                Author notes
                [*]

                These authors contributed equally to this work.

                Article
                srep28509
                10.1038/srep28509
                4926224
                27352851
                85e1b0b5-737c-42ca-a628-31888b0f6d99
                Copyright © 2016, 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
                : 24 September 2015
                : 06 June 2016
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