Towards Selective Agglomeration Detection in Fluidized Beds Using Advanced Signal Analysis Methods

A new methodology of assessing large amounts of fluidized bed pressure fluctuation data with various signal analysis methods in combination with signal pre-treatment methods is presented. This approach can be used to find certain combinations that are selectively sensitive to certain physical effects in fluidized beds, such as agglomeration

Fabrication of Defect-Free P84® Polyimide Hollow Fiber for Gas Separation: Pathway to Formation of Optimized Structure

The elimination of the additional defect healing post-treatment step in asymmetric hollow fiber manufacturing would result in a significant reduction in membrane production cost. However, obtaining integrally skinned polymeric asymmetric hollow fiber membranes with an ultrathin and defect-free selective layer is quite challenging. In this study, P84® asymmetric hollow fiber membranes with a highly thin (~56 nm) defect-free skin were successfully fabricated by fine tuning the dope composition and spinning parameters using volatile additive (tetrahydrofuran, THF) as key parameters. An extensive experimental and theoretical study of the influence of volatile THF addition on the solubility parameter of the N-methylpyrrolidone/THF solvent mixture was performed. Although THF itself is not a solvent for P84®, in a mixture with a good solvent for the polymer, like N-Methyl-2-pyrrolidone (NMP), it can be dissolved at high THF concentrations (NMP/THF ratio > 0.52). The as-spun fibers had a reproducible ideal CO2/N2 selectivity of 40, and a CO2 permeance of 23 GPU at 35 °C. The fiber production can be scaled-up with retention of the selectivity.This research was funded by the European Research Council under the European Union’s Seventh Framework Programme (FP/2007-2013), grant agreement no. 608490, M4CO2 project

Guest-induced structural deformation in Cu-based metal-organic framework upon hydrocarbon adsorption

In a world where capture and separation processes represent above 10% of global energy consumption, novel porous materials, such as Metal-Organic Frameworks (MOFs) used in adsorption-based processes are a promising alternative to dethrone the high-energy-demanding distillation. Shape and size tailor-made pores in combination with Lewis acidic sites can enhance the adsorbate-adsorbent interactions. Understanding the underlying mechanisms of adsorption is essential to designing and optimizing capture and separation processes. Herein, we analyze the adsorption behaviour of light hydrocarbons (methane, ethane, ethylene, propane, and propylene) in two synthesized copper-based MOFs, Cu-MOF-74 and URJC-1. The experimental and computational adsorption curves reveal a limited effect of the exposed metal centers on the olefins. The lower interaction Cu-olefin is also reflected in the calculated enthalpy of adsorption and binding geometries. Moreover, the diamond-shaped pores' deformation upon external stimuli is first reported in URJC-1. This phenomenon is highlighted as the key to understanding the adsorbent's responsive mechanisms and potential in future industrial applications.</p

Zeolite Beta membranes for the separation of hexane isomers

The preparation of a-alumina supported zeolite Beta membranes was successfully achieved and sped up by exploring combinations of three seeding techniques and three synthetic methods. The surface of the membranes was completely covered by well intergrown crystals; the thickness of the zeolite layers ranged from 2 to 6 lm depending on the synthesis method used. The quality of the membranes was tested by means of pervaporation of ethanol/1,3,5-triisopropylbenzene (TIPB) mixtures together with permporometry experiments. The performance in the vapour separation of quaternary equimolar mixtures of nhexane (nHEX), 3-methylpentane (3MP), 2,3-dimethylbutane (23DMB) and 2,2-dimethylbutane (22DMB) in the range 343–443 K showed that permeate flux decreases as the branching degree increases following the order: nHEX 3MP > 23DMB > 22DMB. In the retentate, the fractions of monobranched and normal hexane decrease while the concentration of dibranched isomers is increased compared to the feed composition. The influence of the temperature in the permeation fluxes indicates the existence of an activated transport mechanism which favours the permeation of more nHEX and 3MP with regard to their dibranched isomers. The octane number (ON) of the quaternary mixture was enhanced up to 5 points with the best synthesized membrane

Zeolite Beta Membranes for the Octane Upgrading of C5/C6 Light Naphta

The zeolite Beta membranes were prepared by secondary growth method in asymmetric tubular Al2O3 supports (Inocermic GmbH, Germany), combining three different types of seeding techniques and crystallization conditions. Figure 1 show SEM micrographs of a typical non-calcined beta membrane synthesized in this work (cross section view). The vapour permeation experiments performed in the apparatus shown in Figure 2 with mixtures of nHEX, 3MP, 23DMB and 22DMB show that permeate flux increase as the degree of branching decreases following the order: nHEX>>3MP>23DMB>22DMB. Approximately one third of the feed stream cross the membranes. Figure 3 shows that in the retentate stream the fractions of monobranched and normal hexane isomers (low RON compounds) decrease while the concentration of dibranched isomers (high RON compounds) is increased in relation to the equimolar feed composition. Consequently, the RON can be boosted in retentate up to 3.8 points. These results demonstrate the potential of the zeolite beta membranes for application in the production of additive-free premium gasoline

Experimental evidence of negative linear compressibility in the MIL-53 metal–organic framework family

International audienc

Fischer-Tropsch synthesis over lignin-derived cobalt-containing carbon fiber catalysts prepared in a single step by electrospinning

In the present, work submicron-sized cobalt-containing lignin fibers have been prepared by the electrospinning technique, using Alcell lignin as carbon precursor, a low-cost co-product of the paper making industry. Carbon fibers were obtained by carbonization of Co-containing lignin fibers at different temperatures, yielding cobalt nanoparticles very well dispersed on the carbon fibers surface. These fibrillar catalysts were tested for Low-Temperature FTS using different H2/CO ratiosUniversidad de Málaga. Campus de Excelencia Internacional Andalucía Tech. RTI2018-097555-B-I00 UMA18-FEDERJA-110 P18-RT-459

On the thermal stabilization of carbon-supported SiO2 catalysts by phosphorus:evaluation in the oxidative dehydrogenation of ethylbenzene to styrene and a comparison with relevant catalysts

A strategy to enhance the thermal stability of C/SiO2 hybrids for the O2-based oxidative dehydrogenation of ethylbenzene to styrene (ST) by P addition is proposed. The preparation consists of the polymerization of furfuryl alcohol (FA) on a mesoporous precipitated SiO2. The polymerization is catalyzed by oxalic acid (OA) at 160 °C (FA:OA = 250). Phosphorous was added as H3PO4 after the polymerization and before the pyrolysis that was carried out at 700 °C and will extend the overall activation procedure. Estimation of the apparent activation energies reveals that P enhances the thermal stability under air oxidation, which is a good indication for the ODH tests. Catalytic tests show that the P/C/SiO2 hybrids are readily active, selective and indeed stable in the applied reactions conditions for 60 h time on stream. Coke build-up during the reaction attributed to the P-based acidity is substantial, leading to a reduction of the surface area and pore volume. The comparison with a conventional MWCNT evidences that the P/C/SiO2 hybrids are more active and selective at high temperatures (450–475 °C) while the difference becomes negligible at lower temperature. However, the comparison with reference P/SiO2 counterparts shows a very similar yield than the hybrids but more selective to ST. The benefit of the P/C/SiO2 hybrid is the lack of stabilization period, which is observed for the P/SiO2 to create an active coke overlayer. For long term operation, P/SiO2 appears to be a better choice in terms of selectivity, which is crucial for commercialization

Highly dispersed Ptδ+ on TixCe(1−x)O2 as an active phase in preferential oxidation of CO

Structure–activity relationships for 1 wt.% Pt catalysts were investigated for a series of TixCe(1−x)O2 (x = 1, 0.98, 0.9, 0.5, 0.2 and 0) supports prepared by the sol–gel method. The catalysts prepared by impregnation were characterized in detail by applying a wide range of techniques as N2-isotherms, XRF, XRD, Raman, XPS, H2-TPR, Drifts, UV–vis, etc. and tested in the preferential oxidation of CO in the presence of H2. Also several reaction conditions were deeply analyzed. A strong correlation between catalyst performance and the electronic properties let us to propose, based in all the experimental results, a plausible reaction mechanism where several redox cycles are involved.Financial support from Generalitat Valenciana and Ministerio de Economía y Competitividad (Spain) through projects PROME-TEOII/2014/004 and MAT2010-21147 is gratefully acknowledged. EOJ also thanks the CNPq – Brazil for her grant. EVRF gratefully acknowledge the Ministerio de Economía y Competitividad (Spain) for his Ramon y Cajal grant (RYC-2012-11427)