Publications by authors named "Sara Sorribas"

Combination of the polyimide 6FDA-mPD (6FDA = 4,4'-hexafluoroisopropylidene diphthalic anhydride and mPD = m-phenylenediamine) and crystallites of the metal-organic frameworks (MOFs) MIL-101(Cr) or MOF-199 (HKUST-1, Cu-BTC) produces mixed-matrix membranes (MMMs) with excellent dispersion and compatibility of the MOF particles within the polymer matrix. Permeation tests of a binary CO2/CH4 (50/50) gas mixture showed a remarkable increase of CO2 permeabilities for MIL-101(Cr)@6FDA-mPD and significantly higher selectivities for MOF-199@6FDA-mPD. The CO2 permeability increased from 10 (neat polymer) to 50 Barrer for the 24 wt% MIL-101(Cr)@6FDA-mPD membrane (with essentially constant selectivity) due to the high pore volume of MIL-101(Cr).

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Microporous polymer nanosheets with thicknesses in the range 3-5 nm and with high apparent surface area (Brunauer-Emmett-Teller surface area 940 m g ) are formed when the effectively bifunctional (tetrafluoro) monomer used in the preparation of the prototypical polymer of intrinsic microporosity PIM-1 is replaced with an effectively tetrafunctional (octafluoro) monomer to give a tightly crosslinked network structure. When employed as a filler in mixed-matrix membranes based on PIM-1, a low loading of 0.5 wt% network-PIM-1 nanosheets gives rise to enhanced CO permeability and CO /CH selectivity, compared to pure PIM-1.

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Covalent triazine framework CTF-1 and polysulfone (PSF) are used to form mixed-matrix membranes (MMMs) with 8, 16, and 24 wt% of the porous filler material CTF-1. Studies on permeability and selectivity are carried out concerning the gases O, N, CO, and CH. CO permeability of the synthesized MMMs increases by 5.

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This work reports the fabrication and characterization of Langmuir-Blodgett films of nanoparticles (size 51 ± 10 nm) of the metal organic framework MIL-101(Cr). LB film characterization by SEM, UV-vis, GIXRD, and QCM has shown that the addition of 1 wt % of behenic acid to MOF dispersion allows obtaining dense monolayers at the air-water interface that can be deposited onto solid substrates of different nature with transfer ratios close to 1. Moreover, a QCM-based setup has been built and used for the first time to measure CO2 adsorption isotherms at 303 K on MOF LB films, proving that LB films with MOF masses between 1.

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Mixed-matrix membranes (MMMs) comprising NH-MIL-53(Al) and Matrimid or 6FDA-DAM have been investigated. The MOF loading has been varied between 5 and 20 wt%, while NH-MIL-53(Al) with three different morphologies: nanoparticles, nanorods and microneedles have been dispersed in Matrimid. The synthesized membranes have been tested in the separation of CO from CH in an equimolar mixture.

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Thin-film nanocomposite membranes containing a range of 50-150 nm metal-organic framework (MOF) nanoparticles [ZIF-8, MIL-53(Al), NH2-MIL-53(Al) and MIL-101(Cr)] in a polyamide (PA) thin film layer were synthesized via in situ interfacial polymerization on top of cross-linked polyimide porous supports. MOF nanoparticles were homogeneously dispersed in the organic phase containing trimesoyl chloride prior to the interfacial reaction, and their subsequent presence in the PA layer formed was inferred by a combination of contact angle measurements, FT-IR spectroscopy, SEM, EDX, XPS, and TEM. Membrane performance in organic solvent nanofiltration was evaluated on the basis of methanol (MeOH) and tetrahydrofuran (THF) permeances and rejection of styrene oligomers (PS).

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Silica-(ZIF-8) core-shell spheres with tuneable ordered meso-microporosity have been synthesized, showing that the hydrophobic micropore ZIF-8 shell controls the access of guest molecules into the hydrophilic silica mesoporous structure.

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