The agglomerated nanoparticle layer formed after deposition on th

The agglomerated nanoparticle layer formed after deposition on the inner surface of commercial tubular PLX4032 alumina support was heated under argon for 2 h at 1,000°C for consolidation purposes. The

formation of the carbon-based membrane was easily and visually detected by the formation of a glossy black inner surface. Figure 8 shows the SEM image of the membrane deposited on the asymmetric alumina support (cross-sectional view). The gray coloration of the alumina below the carbon layer clearly indicates the partial infiltration of colloids inside the support during the slip-casting process. The membrane exhibits a homogeneous thickness of about 50 nm. The surface appears to be rough, remembering its colloidal origin (see also Figure 9). Some particles are also observable

on the surface of the layer, which were presumably generated upon breaking the membrane and support Selleckchem Tozasertib system. Figure 8 SEM images of the section (cross-sectional view) of the carbon membrane derived from beer wastes. Figure 9 SEM images of the membrane surface. These were taken before (a) and after (b) heating up at 200°C during gas permeance measurements. The N2 adsorption/desorption isotherm was recorded for the membrane and support system (Figure 10). For that purpose, the alumina support was sanded in order to reveal the contribution of the carbon layer. This curve clearly shows a hysteresis loop featuring the mesoporosity of the layer. This analysis, in the BET approximation, yields a pore diameter of approximately 3.6 nm (low mesoporosity). Dichloromethane dehalogenase However, it is not possible to determine if this measured LY2603618 porosity is only due to the presence of the porous carbon membrane or partially due to the residual

alumina support not totally discarded by sanding. We decided therefore to conduct dynamic water and gas separation measurements. Figure 10 N 2 adsorption/desorption isotherm of the HTC-processed carbon membrane. For a further dynamic characterization of the carbon membrane, water permeability has been measured by recording the water flux through the membrane as a function of the applied nitrogen pressure on the feed solution at room temperature. Figure 11a shows the water flux through the commercial alumina support as a function of the applied pressure, in the range of 3–15 bars. As expected, we obtained an almost linear evolution in which values are in good agreement with the ones reported by the manufacturer. In Figure 11b, the water flux through the carbon membrane deposited on alumina nanofiltration support is evidenced. Figure 11 Water flux as a function of the applied pressure for the different membranes. (a) The starting alumina nanofiltration membrane and (b) the carbon membranes. As illustrated in Figure 11b, no water flux was measured with carbon membranes below 6 bar of applied nitrogen pressure. The measured permeability is 0.005 L h-1·m-2·bar-1, a value which is 1,000 lower than the commercial alumina system.

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