Development of Gas/Liquid Catalytic membrane reactor

La incorporación de nanopartículas metálicas en las membranas puede dotar a las membranas con funciones adicionales y específicos. Modificación de la superficie de la membrana de polietersulfona por injerto UV-asistida de polimerización de ácido acrílico-ha sido realizado con éxito. Catalíticamente activa y eficiente de nanopartículas de Pd tiene-beens sintetizados mediante síntesis intermatrix. Como modelo para la reacción en fase líquida, las TIC comportamiento catalítico fue investigado por la reducción de la acuosa p-nitrofenol a p-aminofenol con borohidruro de sodio como agente reductor. La actividad catalítica de la membrana de Pd incrustado demostró ser directamente proporcional al paladio feliz en el nanocompuesto. La actividad catalítica de reactor de flujo continuo para la reducción de nitrofenol superó al modo por lotes de la operación, ya que se demostró mediante la conversión comparación al mismo nitrofenol concentración inicial y el peso del catalizador. Esto se atribuyó al flujo convectivo de reactivos al sitio catalítico Directamente Todo lo que puede proporcionar un contacto intensivo. Fotoquímico modificado hueco negocio de fibra de microfiltración PES membrana que contiene el catalizador de paladio se aussi probado para la hidrogenación de p-NP como modelo para Gas / Líquido de contacto. Sin embargo, la reacción no tuvo éxito, y esto podría estar relacionado a nuestras condiciones experimentales. Debido al hecho de que el agua no es un buen medio de reacción para la reacción de hidrogenación utilizando hidrógeno gaseoso, las especies reaccionantes pueden no ser bien absorbidos por la superficie del catalizador. Como la solubilidad del hidrógeno en metanol puro y etanol es significativamente mayor que en agua, la prueba en cualquiera de los disolventes podría ser una solución

Effects of some ion-specific properties in the electrocoagulation process with aluminum electrodes

The influence of anion specificity on the faradaic efficiency relative to aluminum oxidation during electrocoagulation has been reported. While with chaotrope anions, the faradaic efficiency is higher than 1, it is lower than 1 with kosmotrope anions. The origin of this distinction has been ascribed to the ability of anions to cause pitting through the thin passive film at the aluminum surface, which depends on the varying resistance of the anions to dehydration. The influence of the nature of the cation of the supporting electrolyte on the efficiency of electrocoagulation has been investigated by comparing the same treatment of two characteristic colloidal samples. While removal efficiency is better for a positively charged latex in the presence of sodium chloride, it is better for a negatively charged oil in water emulsion in the presence of ammonium chloride. The results come from different effects of pH and its influence on aluminum species during electrocoagulation

Influence of the Counterion Nature on the Stability Sequence of Hydrophobic Latex Particles

The aggregation kinetics of negatively charged polystyrene latex particles in the presence of monovalent electrolytes have been investigated. The inferred coagulation critical concentrations were compared to establish the stability sequence. With the same representative co-ions, this sequence is reversed when using kosmotrope sodium and chaotrope potassium cations. The results have been ascribed to a variable competition of the co-ions toward the hydrophobic surface depending on the lyotropic nature of the associated counterion. They provide new insights into the implication of ionic specificity in the stability behavior of aqueous dispersions of charged colloids

Membrane modules for CO2 capture based on PVDF hollow fibers with ionic liquids immobilized

Hollow fiber membrane contactors with ionic liquids are promising alternatives to traditional spray towers and amines for carbon dioxide absorption. Ionic liquids have emerged as new alternative solvents because of their zero emission features compared with amines. The aim of this work was to compare fibers based on PVDF and different additives, as well as fibers including two different ionic liquids. On the one hand, 1-ethyl-3-methylimidazolium ethyl sulfate [emim][EtSO4] presents physical absorption, and on the other hand, 1-ethyl-3-methylimidazolium acetate [emim][Ac] presents chemical absorption. To compare the fibers under study, the thickness of the composite fiber was examined using scanning electron microscopy (SEM). The mechanical properties and the bubble point were also evaluated. Permeability tests were conducted, and the gas permeation of the composite hollow fibers was measured using pure CO2. Laboratory-made stainless steel modules were used for the tests. All of the above tests were performed with the fibers in both wet and dry conditions. It was determined that the fibers with the ionic liquid immobilized would be promising for CO2 capture because the CO2 permeance significantly increased. Namely, D+[emim][EtSO4] achieved a 43% increase compared with the fibers without the addition of the ionic liquid, resulting in a CO2 permeance value of 57040NL/(hm2bar), which is higher than the values reported in the literature for PVDF. Moreover, the overall mass transfer coefficient for CO2 capture using the D+[emim][Ac] fibers also presented highly competitive values.This research has been funded by the Spanish Ministry Economy and Competitiveness (Projects ENE2010-14828 and CTQ2013-48280-C3-1-R)

Remarkable catalytic activity of polymeric membranes containing gel-trapped palladium nanoparticles for hydrogenation reactions

Polymeric flat-sheet membranes and hollow fibers were prepared via UV photo-initiated polymerization of acrylic acid at the surface of commercial polyether sulfones (PES) membranes. These polymeric materials permitted to immobilize efficiently palladium nanoparticles (PdNP), which exhibited a mean diameter in the range of 4−6 nm. These materials were synthesized by chemical reduction of Pd(II) precursors in the presence of the corresponding support. We successfully applied the as-prepared catalytic materials in hydrogenation reactions under continuous flow conditions. Flat sheet membranes were more active than hollow fibers due to the flow configuration and defavorable operating conditions. Actually, various functional groups (i.e. CC, CC and NO2) were reduced in flow-through configuration, under mild conditions (between 1.4 and 2.2 bar H2 at 60 °C, using 3.2 mol% of Pd loading), archiving high conversions in short reaction times (12−24 s)

Development of double porous poly (ε - caprolactone)/chitosan polymer as tissue engineering scaffold

Polymer blend made from poly( - caprolactone)/chitosan (PCL/CHT) offers interesting opportunities for biological applications. The paper presents a new way to fabricate PCL/CHT double-porosity (macrovoids with interconnected microporosity) membrane materials from a chemical optimization of the solvent and non-solvent phases and from a modified phase inversion technique. By varying the PCL/CHT proportion, it is shown that it is possible to improve the chemical and physical properties of the CHT carbohydrate polymer. The PCL/CHT membranes are fully characterized in term of physico-chemical properties (ATR-FTIR, XRD and DSC) to understand the miscibility of the two-polymer blend. Morphological characterization by SEM shows that by increasing CHT wt% in the blend, the size of the macrovoids was increasing. Rapid enzymatic degradation of PCL from all the blend was found by using lipase (from P. cepacia). The mechanisms at the origin of the morphological structuration of the material is also discussed. To test the ability to operate these materials as small diameter vascular scaffolds, cell culture with human umbilical vein endothelial cells (HUVECs) were carried out on the membrane and the results analyzed with laser scanning confocal microscopy (LSCM). Data suggest that the blend membrane with higher concentration of CHT polymer wt% have suitable properties that promote high number of cells on the surface by maintaining cellular cytoskeleton integrity within 3 days. The blend membrane with a double porous morphology could be potentially applicable in future for small diameter vascular graft application. The surface macrovoids (20–90 μm) could be useful for three-dimensional cellular adhesion and proliferation and interconnected microporous spongy network (7–20 μm) is expected to transfer essential nutrients, oxygen, growth factor between the macrovoids and the supernatant

Double porous poly (Ɛ-caprolactone)/chitosan membrane scaffolds as niches for human mesenchymal stem cells

In this paper, we developed membrane scaffolds to mimic the biochemical and biophysical properties of human mesenchymal stem cell (hMSC) niches to help direct self-renewal and proliferation providing to cells all necessary chemical, mechanical and topographical cues. The strategy was to create three-dimensional membrane scaffolds with double porosity, able to promote the mass transfer of nutrients and to entrap cells. We developed poly (Ɛ-caprolactone) (PCL)/chitosan (CHT) blend membranes consisting of double porous morphology: (i) surface macrovoids (big pores) which could be easily accessible for hMSCs invasion and proliferation; (ii) interconnected microporous network to transfer essential nutrients, oxygen, growth factors between the macrovoids and throughout the scaffolds. We varied the mean macrovoid size, effective surface area and surface morphology by varying the PCL/CHT blend composition (100/0, 90/10, 80/20, 70/30). Membranes exhibited macrovoids connected with each other through a microporous network; macrovoids size increased by increasing the CHT wt%. Cells adhered on the surfaces of PCL/CHT 100/0 and PCL/CHT 90/10 membranes, that are characterized by a high effective surface area and small macrovoids while PCL/CHT 80/20 and PCL/CHT 70/30 membranes with large macrovoids and low effective surface area entrapped cells inside macrovoids. The scaffolds were able to create a permissive environment for hMSC adhesion and invasion promoting viability and metabolism, which are important for the maintenance of cell integrity. We found a relationship between hMSCs proliferation and oxygen uptake rate with surface mean macrovoid size and effective surface area. The macrovoids enabled the cell invasion into the membrane and the microporosity ensured an adequate diffusive mass transfer of nutrients and metabolites, which are essential for the long-term maintenance of cell viability and functions

Tunable microstructured membranes in organ‐on‐chip to monitor trans‐endothelial hydraulic resistance

Tissue engineering is an interdisciplinary field, wherein scientists from different backgrounds collaborate to address the challenge of replacing damaged tissues and organs through the in vitro fabrication of functional and transplantable biological structures. Because the development and optimization of tissue engineering strategies rely on the complex interaction of cells, materials, and the physical–chemical tissue microenvironment, there is a need for experimental models that allow controlled studies of these aspects. Organs-on-chips (OOCs) have recently emerged as in vitro models that capture the complexity of human tissues in a controlled manner, while including functional readouts related to human organ physiology. OOCs consist of multiple microfluidic cell culture compartments, which are interfaced by porous membranes or hydrogels in which human cells can be cultured, thereby providing a controlled culture environment that resembles the microenvironment of a certain organ, including mechanical, biochemical, and geometrical aspects. Because OOCs provide both a well-controlled microenvironment and functional readouts, they provide a unique opportunity to incorporate, evaluate, and optimize materials for tissue engineering. In this study, we introduce a polymeric blend membrane with a three-dimensional double-porous morphology prepared from a poly(ɛ-caprolactone)–chitosan blends (PCL–CHT) by a modified liquid-induced phase inversion technique. The membranes have different physicochemical, microstructural, and morphological properties depending on different PCL–CHT ratios. Big surface pores (macrovoids) provide a suitable microenvironment for the incorporation of cells or growth factors, whereas an interconnected small porous (macroporous) network allows transfer of essential nutrients, diffusion of oxygen, and removal of waste. Human umbilical vein endothelial cells were seeded on the blend membranes embedded inside an OOC device. The cellular hydraulic resistance was evaluated by perfusing culture medium at a realistic transendothelial pressure of 20 cmH2O or 2 kPa at 37°C after 1 and 3 days postseeding. By introducing and increasing CHT weight percentage, the resistance of the cellular barrier after 3 days was significantly improved. The high tuneability over the membrane physicochemical and architectural characteristics might potentially allow studies of cell–matrix interaction, cell transportation, and barrier function for optimization of vascular scaffolds using OOCs

Homopolymérisation et copolymérisation de macromonomères de polystyrène par catalyse de métaux de transition

STRASBOURG-Sc. et Techniques (674822102) / SudocSudocFranceF