639 research outputs found

    Synthesis, characterisation and gas permeation studies on microporous silica and alumina-silica membranes for separation of propane and propylene

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    Microporous silica membranes are known to exhibit molecular sieving effects. However, separation of nearly equal sized molecules is difficult to carry out by size exclusion. Introducing sorption selectivity and keeping the kinetics favourable to facilitate a good contribution of permeation from sorption is a possible solution to enhance selectivity of adsorbing molecules. Results are presented in this paper on the synthesis of a microporous silica membrane with commendable permselectivity between helium and propylene. Modifications are performed on the membrane to improve its almost non-selective nature to propylene/propane mixtures to give practical separation values. Gas separation results on the modified membranes are presented. Surface selectivity on the newly added alumina surface layer is identified as the helping mechanism in realising this separation

    Characterization of Grain Boundaries in Superplastically Deformed Y-TZP Ceramics

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    The effects of compressive deformation on the grain boundary characteristics of fine-grained Y-TZP have been investigated using surface spectroscopy, impedance analysis, and transmission electron microscopy. After sintering at low temperature (1150°C), the grain boundaries are covered by an ultrathin (1nm) yttrium-rich amorphous film. After deformation at 1200°–1300°C under low stress, some grain boundaries are no longer covered by the amorphous film. Yttrium segregation seems to occur only at wetted grain boundaries. Evidence has been found that the extent of dewetting increases with increasing applied stress

    Textural evolution and phase transformation in titania membranes: Part 1. -unsupported membranes

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    Textural evolution in sol–gel derived nanostructured unsupported titania membranes has been studied using differential scanning calorimetry (DSC), differential thermal analysis (DTA), thermal gravimetry (TG), X-ray diffraction (XRD) and N2 adsorption. The anatase-to-rutile phase transformation kinetics were studied using the Avrami model. The precursor gel had a surface area of ca. 165 m2 g–1, which after heat treatment at 600 °C for 8 h reduced to zero. Undoped titania-gel layers transformed to more than 95% rutile after calcination at 600 °C for 8 h. The causes of surface-area reduction and pore growth were anatase crystallite growth and the enhanced sintering of rutile during transformation. Lanthanum oxide was identified as a suitable dopant for shifting the transformation temperature to ca. 850 °C. Lanthanum oxide doped titania showed an improved stability of porous texture compared to that of the undoped titania membranes

    Kinetics and morphology of electrochemical vapour deposited thin zirconia/yttria layers on porous substrates

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    By means of electrochemical vapour deposition (EVD), it is possible to grow thin (0.5-5 ”m), dense zirconia/yttria layers on porous ceramic substrates. Kinetics of the EVD process, morphology and oxygen permeation properties of the grown layers are investigated. Very thin (~ 0.5 ”m) layers are grown at relatively low temperatures (700-800 °C). Water vapour as reactant enhances the surface reaction rate at the solid oxide/oxygen source reactant interface. A transition occurs from pore diffusion (above 1000 °C) to bulk electrochemical diffusion (below 900 °C) as rate-limiting step for layer growth. The zirconia/yttria solid solution is mainly deposited in the cubic phase; the layers grow in a typical columnar way and are polycrystalline. Oxygen permeation measurements show that the oxygen permeation flux through the zirconia/yttria layers is influenced by the layer thickness, morphology, presence of water vapour and the oxygen pressure gradient over the layer

    Application of chicken microarrays for gene expression analysis in other avian species

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    BACKGROUND: With the threat of emerging infectious diseases such as avian influenza, whose natural hosts are thought to be a variety of wild water birds including duck, we are armed with very few genomic resources to investigate large scale immunological gene expression studies in avian species. Multiple options exist for conducting large gene expression studies in chickens and in this study we explore the feasibility of using one of these tools to investigate gene expression in other avian species. RESULTS: In this study we utilised a whole genome long oligonucleotide chicken microarray to assess the utility of cross species hybridisation (CSH). We successfully hybridised a number of different avian species to this array, obtaining reliable signals. We were able to distinguish ducks that were infected with avian influenza from uninfected ducks using this microarray platform. In addition, we were able to detect known chicken immunological genes in all of the hybridised avian species. CONCLUSION: Cross species hybridisation using long oligonucleotide microarrays is a powerful tool to study the immune response in avian species with little available genomic information. The present study validated the use of the whole genome long oligonucleotide chicken microarray to investigate gene expression in a range of avian species

    Bulk and electrochemical properties of BiVO4

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    The mixed (oxygen ionic-electronic) conductor bismuth vanadate (BiVO4) was studied with respect to its electrochemical properties. The ionic transference numbers, measured by the concentration cell method in the temperature range of 800 to 1000 K, vary from 0.7 to 0.3. The total conductivity of this ceramic material isone order of magnitude lower than found for cubic yttria-stabilized zirconia (YSZ). The activation enthalpy for the electronic conductivity is high (193 kJ/mol) compared to the ionic conductivity (71 kJ/mol). The PO2 dependence of the conductivity data in combination with the Seebeck measurements showed electrons to be the majority charge carriers, indicating that BiVO4 is an n-type mixed conductor

    Modelling and analysis of CVD processes for ceramic membrane preparation

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    A mathematical model is presented that describes the modified chemical vapour deposition (CVD) process (which takes place in advance of the electrochemical vapour deposition (EVD) process) to deposit ZrO2 inside porous media for the preparation and modification of ceramic membranes. The isobaric model takes into account intrapore Knudsen diffusion of ZrCl4 and H2O, which enter the membrane from opposite sides, and Langmuir-Hinshelwood reaction of the solid product ZrO2 on the internal pore wall. The processes occurring in one single pore are investigated, and the change in pore geometry during deposition is taken into account. Based upon this model, the deposition profile is studied. The model fits reasonably well with experimental results

    Pore Narrowing and Formation of Ultrathin Yttria-Stabilized Zirconia Layers in Ceramic Membranes by Chemical Vapor Deposition/Electrochemical Vapor Deposition

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    Chemical vapor deposition (CVD) and electrochemical vapor deposition (EVD) have been applied to deposit yttria-stabilized-zirconia (YSZ) on porous ceramic media. The experimental results indicate that the location of YSZ deposition can be varied from the surface of the substrates to the inside of the substrates by changing the CVD/EVD experimental conditions, i.e., the concentration ratio of the reactant vapors. The deposition width is strongly dependent on the deposition temperature used. The deposition of YSZ inside the pores resulted in pore narrowing and eventually pore closure, which was measured by using permpor-ometry. However, deposition of YSZ on top of porous ceramic substrates (outside the pores) did not result in a reduction of the average pore size. Ultrathin, dense YSZ layers on porous ceramic substrates can be obtained by suppressing the EVD layer growth process after pore closure

    Synthesis and textural properties of unsupported and supported rutile (TiO2) membranes

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    Two approaches were postulated for improving the stability of porous texture of titania membranes: (1) retarding the phase transformation and grain growth; (2) avoiding the phase transformation. Based on the second approach, rutile membranes were made directly from a rutile sol, prepared by the precipitation of titania on SnO2 nuclei. The rutile membranes were stable up to 800 °C, with a porosity of ca. 40%, whereas normal titania membranes (starting with anatase) show very little porosity above 600 °C. Alumina substitution retards grain growth and pore growth at 850 °C for unsupported as well as supported membranes. \u

    High-temperature catalyst supports and ceramic membranes: Metastability and particle packing

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    Parameters and/or processes responsible for the stability of catalyst supports and ceramic membranes are discussed. Two major parameters/processes were identified which are responsible for the stability of sol-gel derived nanostructured oxides at elevated temperatures. They are metastable-to-stable phase transformation and structure and packing of primary particles within the aggregate. Based on these observations, strategies to develop thermostable nanostructured oxides for high-temperature membrane and catalyst applications are discussed by taking titania and titania-alumina nanocomposites as examples
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