130 research outputs found
Breaking through permeability–selectivity trade-off of thin-film composite membranes assisted with crown ethers
Metal-organic framework based mixed matrix membranes: a solution for highly efficient CO2 capture?
The field of metal-organic framework based mixed matrix membranes (M(4)s) is critically reviewed, with special emphasis on their application in CO2 capture during energy generation. After introducing the most relevant parameters affecting membrane performance, we define targets in terms of selectivity and productivity based on existing literature on process design for pre- and post-combustion CO2 capture. Subsequently, the state of the art in M(4)s is reviewed against these targets. Because final application of these membranes will only be possible if thin separation layers can be produced, the latest advances in the manufacture of M-4 hollow fibers are discussed. Finally, the recent efforts in understanding the separation performance of these complex composite materials and future research directions are outlined.European Commission FP7 608490
ERC 33574
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A solution-processable and ultra-permeable conjugated microporous thermoset for selective hydrogen separation.
The synthesis of a polymer that combines the processability of plastics with the extreme rigidity of cross-linked organic networks is highly attractive for molecular sieving applications. However, cross-linked networks are typically insoluble or infusible, preventing them from being processed as plastics. Here, we report a solution-processable conjugated microporous thermoset with permanent pores of ~0.4 nm, prepared by a simple heating process. When employed as a two-dimensional molecular sieving membrane for hydrogen separation, the membrane exhibits ultrahigh permeability with good selectivity for H2 over CO2, O2, N2, CH4, C3H6 and C3H8. The combined processability, structural rigidity and easy feasibility make this polymeric membrane promising for large-scale hydrogen separations of commercial and environmental relevance
Electrospun nanofiber substrates that enhance polar solvent separation from organic compounds in thin‐film composites
Tailoring molecular interactions between microporous polymers in high performance mixed matrix membranes for gas separations
Ultem®/ZIF-8 Mixed Matrix Membranes for Gas Separation: Transport and Physical Properties
Pembuatan Karbon Aktif dari Cangkang Kelapa Sawit dengan Aktivator H3PO4
Penelitian ini bertujuan untuk mengetahui kondisi optimum karbon aktif yang
terbuat dari cangkang kelapa sawit yang diaktivasi dengan H3PO4 berdasarkan
bilangan iodin. Metodologi penelitian meliputi proses penyiapan bahan baku,
aktivasi, pirolisis dan pengujian. Tahap aktivasi dilakukan dengan variasi
konsentrasi aktivator H3PO4, yaitu 10 %, 15 %, 20 % dan 25 %. Tahap pirolisis
dilangsungkan dengan variasi suhu pirolisis 300 oC, 400 oC, 500 oC dan 600 oC
serta dengan variasi waktu pirolisis yaitu 1 jam, 1,5 jam, 2 jam, dan 2,5 jam.
Pengujian dilakukan dengan uji bilangan iodin karbon aktif metode standar
ASTM D 4607 - 94 modified. Hasil penelitian menunjukkan bahwa kondisi
operasi optimum, yaitu konsentrasi aktivator H3PO4 20 %, suhu pirolisis 400_oC
dan waktu pirolisis 1 jam menghasilkan bilangan iodin tertinggi sebesar
403,5_mg/g.67 HalamanSkripsi Sarjan
Mixed matrix membranes containing MOF's for ethelyne/ethane separation. Part B: Effect of CU3BTC2 on membrane transport properties
Mixed matrix membranes (MMMs) containing various amounts of the metal-organic framework (MOF) Cu3BTC2 as filler in P84 were characterized in terms of their ethylene and ethane separating performance. Previous research showed that especially the use of the MOF Cu3BTC2 improves the ethylene/ethane separating ability due its selective interaction with the olefin. Although the ethylene permeability remained constant, the ethylene/ethane permeability selectivity significantly increased to a value of 7.1 with increasing Cu3BTC2 loading. Experiments show that the ethylene solubility coefficient increased from 1.0 to 2.9×10−3 mol/(m3 Pa) with increasing Cu3BTC2 loading up to 20 wt%. Since the ethylene permeability coefficient remained constant at 17×10−18 mol m/(m2 s Pa) with increasing Cu3BTC2 loading, the ethylene diffusion coefficient was calculated to decrease by a factor of three. Evaluation of the reason for the strong increase in permeability selectivity with increasing Cu3BTC2 loading revealed that this is the result of an increase in diffusion selectivity by a factor of two. These results suggest immobilization of ethylene inside the MOF particles as the result of strong ethylene–copper(II) MOF interactions.\u
Mixed matrix membranes containing MOF's for ethelyne/ethane separation. Part A: Membrane preparation and characterization
Mixed matrix membranes (MMMs) containing three different metal organic frameworks (MOFs) (Cu3BTC2, FeBTC and MIL-53 (Al)) as filler in P84 were prepared and characterized in terms of ethylene/ethane separating ability. SEM, TGA and DSC suggest the absence of non-selective voids in the Cu3BTC2 and FeBTC MMMs. Gas permeation experiments confirmed this, and showed an increase in ethylene/ethane selectivity of 73% to a value of 7.1, while ethylene permeability remained constant at 17×10−18 mol m/(m2 s Pa) with addition of 20 wt% Cu3BTC2. Addition of 20 wt% FeBTC showed a reduced permeability, caused by the formation of a denser intermediate layer, and no significant change in selectivity. Addition of MIL-53 led to increased permeabilities and no change in selectivity, which is probably the result of the formation of non-selective voids or the absence of inherent selectivity of MIL-5
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