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In-Young Jang Oh-Hwan Kweon Kyoung-Eon Kim Gab-Jin Hwang Sang-Bong Moon An-Soo Kang 《Journal of membrane science》2008,322(1):154-161
The ion exchange membrane using polysulfone (PSf) and polyether ether ketone (PEEK) as a basic material was prepared to apply in the polymer electrolyte membrane electrolysis (PEME). The sulfonated block copolymer of PSf and poly(phenylene sulfide sulfone) (SPSf-co-PPSS) and the sulfonated PEEK (SPEEK) were blended with tungstophosphoric acid (TPA) to avoid water swelling at elevated temperatures led to decrease in mechanical strength. These prepared ion exchange membranes showed some interesting characteristics including physicochemical stabilities, mechanical and membrane properties.The prepared ion exchange membrane was utilized to prepare the membrane electrode assembly (MEA). MEA consisted of Pt/PEM/Pt was prepared by equilibrium and non-equilibrium impregnation–reduction (I–R) methods. The prepared MEA by non-equilibrium I–R method was used in the PEME unit cell. The cell voltages of the MEA using SPSf-co-PPSS/TPA and SPEEK/TPA membranes were 1.83 V and 1.90 V at 1 A/cm2 and 80 °C, with platinum loadings of 1.12 and 1.01 mg/cm2, respectively. 相似文献
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Monolithic metal–organic framework MIL‐53(Al)‐polymethacrylate composite column for the reversed‐phase capillary liquid chromatography separation of small aromatics
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Kareem Yusuf Ahmed Yacine Badjah‐Hadj‐Ahmed Ahmad Aqel Zeid Abdullah ALOthman 《Journal of separation science》2016,39(5):880-888
A monolithic capillary column containing a composite of metal–organic framework MIL‐53(Al) incorporated into hexyl methacrylate‐co‐ethylene dimethacrylate was prepared to enhance the separation of mixtures of small aromatic compounds by using capillary liquid chromatography. The addition of 10 mg/mL MIL‐53(Al) microparticles increased the micropore content in the monolithic matrix and increased the Brunauer–Emmett–Teller surface area from 26.92 to 85.12 m2/g. The presence of 1,4‐benzenedicarboxylate moieties within the structure of MIL‐53(Al) as an organic linker greatly influenced the separation of aromatic mixtures through π–π interactions. High‐resolution separation was obtained for a series of alkylbenzenes (with resolution factors in the range 0.96–1.75) in less than 8 min, with 14 710 plates/m efficiency for propylbenzene, using a binary polar mobile phase of water/acetonitrile in isocratic mode. A reversed‐phase separation mechanism was indicated by the increased retention factor and resolution as the water percentage in the mobile phase increased. A stability study on the composite column showed excellent mechanical stability under various conditions. The higher resolution and faster separation observed at increased temperature indicated an exothermic separation, whereas the negative values for the free energy change of transfer indicated a spontaneous process. 相似文献
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Back Cover: Ligand Symmetry Modulation for Designing a Mesoporous Metal–Organic Framework: Dual Reactivity to Transition and Lanthanide Metals for Enhanced Functionalization (Chem. Eur. J. 27/2015)
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Prof. Miao Du Xi Wang Dr. Min Chen Dr. Cheng‐Peng Li Jia‐Yue Tian Zhuo‐Wei Wang Prof. Chun‐Sen Liu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(27):9916-9916