Carbon electrochemical membrane functionalized with flower cluster-like FeOOH catalyst for organic pollutants decontamination.

Decorating active catalysts on the reactive electrochemical membrane (REM) is an effective way to further improve its decontamination performance. In this work, a novel carbon electrochemical membrane (FCM-30) was prepared through coating FeOOH nano catalyst on a low-cost coal-based carbon membrane (CM) through facile and green electrochemical deposition. Structural characterizations demonstrated that the FeOOH catalyst was successfully coated on CM, and it grew into a flower cluster-like morphology with abundant active sites when the deposition time was 30 min. The nano FeOOH flower clusters can obviously boost the hydrophilicity and electrochemical performance of FCM-30, which enhance its permeability and bisphenol A (BPA) removal efficiency during the electrochemical treatment. Effects of applied voltages, flow rates, electrolyte concentrations and water matrixes on BPA removal efficiency were investigated systematically. Under the operation condition of 2.0 V applied voltage and 2.0 mL·min-1 flow rate, FCM-30 can achieve the high removal efficiency of 93.24% and 82.71% for BPA and chemical oxygen demand (COD) (71.01% and 54.89% for CM), respectively, with only a low energy consumption (EC) of 0.41 kWh·kgCOD-1, which can be ascribed to the enhancement on OH yield and direct oxidation ability by the FeOOH catalyst. Moreover, this treatment system also exhibits good reusability and can be adopted on different water background as well as different pollutants.

Dialytic Synthesis of Two-Dimensional Cu-Based Metal-Organic Frameworks for Gas Separation: Designable MOF-Polymer Interface.

We demonstrate a dialytic strategy for the synthesis of congeneric two-dimensional metal-organic framework (2D MOF) nanosheets with a dialysis membrane using 1,4-benzenedicarboxylic acid (BDC), 1,4-naphthalenedicarboxylic acid (NDC), and 9,10-anthracenedicarboxylic acid (ADC) as organic linkers and copper(II) as a metal precursor, respectively. Polyimide (PI) membranes containing these empty 2D MOF nanosheets exhibit distinct molecular sieve effects. Molecular dynamic simulation results reveal that the structures of MOF-polymer interfaces are designable by modifying the MOF interlayer distance and aperture size, which has significant influences on gas permeability and selectivity. As a result, Cu-NDC/PI with the moderate composite interface structure shows superior performance toward H2/CH4 and CO2/CH4 separations with a selectivity of 199 and 63 over Cu-BDC (121 and 53) and Cu-ADC (135 and 54), respectively.

High performance polypyrrole coated carbon-based electrocatalytic membrane for organic contaminants removal from aqueous solution.

Electrocatalytic filtration process adopting the electrocatalytic membrane as both filtration membrane and active electrode showed great prospect on the organic pollutant removal from water. In this work, a high-performance metal-free polypyrrole (PPy) coated carbon-based electrocatalytic membrane (PPy@CCM) was developed through the facile and controllable electro-polymerization deposition method. Structural properties and electrochemical performance of the prepared PPy@CCM were characterized systematically. The influences of preparation parameters and operational parameters on water treatment performance of PPy@CCM were also investigated. Results indicates that the spherical PPy particles uniformly distributed on the surface of PPy@CCM. Coating with PPy particles can significantly improve the hydrophilicity and electrochemical activity of CCM, therefore PPy@CCM has lower hydraulic resistance and higher water treatment performance than CCM. The phenol and chemical oxygen demand (COD) removal rates obtained by PPy@CCM are up to 99.51% and 89.90%, respectively, under the optimal condition of 2.0 V cell potential, 2.50 g·L-1 Na2SO4, 1.5 ml·min-1 flow rate and 50 mg·L-1 phenol, and only 0.5 kWh·kgCOD-1 energy consumption is consumed. In addition, PPy@CCM also exhibits good treatment performance in different water matrixes. Moreover, PPy@CCM has good stability for several cycle operation and considerable applicability for different types of organic pollutants removal. The oxidation mechanism study reveals that PPy@CCM has both direct and indirect oxidation activity during the electrocatalytic filtration treatment, and the coating of PPy can improve the direct oxidation ability and ·OH yield of CCM.

A Review on the Progress in Nanoparticle/C Hybrid CMS Membranes for Gas Separation.

Carbon molecular sieve (CMS) membranes are novel materials derived from the pyrolysis of the polymeric precursors and have a well-developed ultra-microporous structure that can separate small gas pairs with minor difference in diameter, and thus exhibit higher gas permeability and selectivity than polymeric membranes. However, the gas permeability for traditional pure CMS membranes now cannot satisfy the requirements of commercial applications due to their disordered pore structure and high gas molecular diffusion resistance. Incorporating functional materials into membrane precursors to fabricate hybrid CMS membranes has been regarded as an effective way to tune the disordered pore structure of traditional pure CMS membranes, and thus to greatly improve their gas permeability. Many nanoparticles have been tested as the functional foreign materials to fabricate the hybrid CMS membranes with more developed microporous structure and enhanced gas separation performance. This review discusses the hybridized nanoparticle selection and effect of the species, quantities and particle sizes of the foreign materials on CMS membrane characteristics and performance. The function of the materials incorporated inside the hybrid CMS membranes is also analyzed. It is identified that preparation of hybrid CMS membranes provides a simple and convenient route to efficiently improve the trade-off relationship between permeability and selectivity, and to enable the construction of carbon-based composite materials with novel functionalities in membrane science.