Academic literature on the topic 'Oxide supported oxide'

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Journal articles on the topic "Oxide supported oxide"

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Cochran, SJ, and FP Larkins. "An X-Ray Photoelectron Study of Doped and Supported Nickel Oxide." Australian Journal of Chemistry 38, no. 9 (1985): 1293. http://dx.doi.org/10.1071/ch9851293.

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The surfaces of lithium-and chromium-doped nickel oxide and of nickel oxide supported on alumina have been examined by X-ray photoelectron spectroscopy. The concentration of the nickel(III) species increased for the lithium-doped oxide and decreased for the chromium-doped oxide relative to the undoped oxide. The effects of doping were manifested most clearly however by the amount of oxygen-containing species adsorbed on the oxide surface rather than by variations in the nickel(III) peak intensity. Lithium-doped oxides were also shown to reduce more readily than undoped or chromium-doped oxides
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Zhong, Liang, and Gaik-Khuan Chuah. "Fischer Indole Synthesis over Hydrous Zirconia-Supported Niobium Oxide." Australian Journal of Chemistry 62, no. 9 (2009): 1027. http://dx.doi.org/10.1071/ch09237.

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Supported niobium oxides are investigated as green catalysts for Fischer indole reaction. By means of wet impregnation, 10–40 wt-% Nb2O5 were loaded onto hydrous zirconia as a support. Pore size distribution curves showed that the niobium oxide overlayer was uniformly dispersed onto the mesoporous support. Samples with close to a monolayer coverage of niobium oxide had the highest activity in the Fischer indole reaction of phenylhydrazine with both 3-heptanone and cyclohexanone. A coverage higher than a monolayer led to lower activity. In comparison, the supported catalysts were more active th
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Wayne Goodman, D. "Surface spectroscopic studies of model supported-metal catalysts." Proceedings, annual meeting, Electron Microscopy Society of America 53 (August 13, 1995): 394–95. http://dx.doi.org/10.1017/s0424820100138348.

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A new surface science approach to the study of supported-metal catalysts will be described. Thin oxide films (~100 Å) of SiO2, Al2O3, or MgO supported on a refractory metal substrate (e.g., Mo or W) have been prepared by depositing the oxide metal precursor in a background of oxygen (ca. l×l0-5 Torr) [1]. The thin-film catalysts facilitate investigation by an array of surface techniques, many of which are precluded when applied to the corresponding bulk oxide [1,2]. In particular, the oxide films have been characterized by AES, ELS, HREELS, XPS, UPS, ISS, IRAS, and TD spectroscopies and shown
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Sun, Qiang, Zhong Wang, Da Wang, Zhe Hong, Mingdong Zhou, and Xuebing Li. "A review on the catalytic decomposition of NO to N2 and O2: catalysts and processes." Catalysis Science & Technology 8, no. 18 (2018): 4563–75. http://dx.doi.org/10.1039/c8cy01114a.

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Recent advances in the catalytic decomposition of NO have been overviewed and divided into three categories: metal oxide catalysts (including perovskites and rare earth oxides), supported metal oxide catalysts (including alkali metals, cobalt oxide and noble metals) and Cu-ZSM-5.
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Guimond, S., M. Abu Haija, S. Kaya, et al. "Vanadium oxide surfaces and supported vanadium oxide nanoparticles." Topics in Catalysis 38, no. 1-3 (2006): 117–25. http://dx.doi.org/10.1007/s11244-006-0076-8.

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McKee, Clive. "Model oxide-supported catalysts." Applied Catalysis A: General 155, no. 2 (1997): N10—N11. http://dx.doi.org/10.1016/s0926-860x(97)90427-0.

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Takagaki. "Rational Design of Metal Oxide Solid Acids for Sugar Conversion." Catalysts 9, no. 11 (2019): 907. http://dx.doi.org/10.3390/catal9110907.

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Aqueous-phase acid-catalyzed reactions are essential for the conversion of cellulose-based biomass into chemicals. Brønsted acid and Lewis acid play important roles for these reactions, including hydrolysis of saccharides, isomerization and epimerization of aldoses, conversion of d-glucose into 5-hydroxymethylfurfural, cyclodehydration of sugar alcohols and conversion of trioses into lactic acid. A variety of metal oxide solid acids has been developed and applied for the conversion of sugars so far. The catalytic activity is mainly dependent on the structures and types of solid acids. Amorphou
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Blanco, J., J. F. Garcia de la Banda, P. Avila, and F. Melo. "Selective reduction of nitric oxide on nickel oxide-copper oxide supported catalysts." Journal of Physical Chemistry 90, no. 20 (1986): 4789–93. http://dx.doi.org/10.1021/j100411a016.

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Saroyan, Hayarpi, Dimitra Ntagiou, Kyriazis Rekos, and Eleni Deliyanni. "Reactive Black 5 Degradation on Manganese Oxides Supported on Sodium Hydroxide Modified Graphene Oxide." Applied Sciences 9, no. 10 (2019): 2167. http://dx.doi.org/10.3390/app9102167.

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Sodium hydroxide-modified graphene oxide was used as manganese oxides support for the preparation of nanocomposites via a one-pot preparation route for the degradation of Reactive Black 5. The nanocomposites were characterized for their structure by X-ray diffraction, for their textural properties by Nitrogen adsorption, and for their surface chemistry by Fourier transform infrared spectroscopy, potentiometric titration, and thermal analysis measurements. The nanocomposites prepared showed to possess high activity for the degradation/oxidation of Reactive Black 5 at ambient conditions, without
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Saroyan, Hayarpi, George Kyzas, and Eleni Deliyanni. "Effective Dye Degradation by Graphene Oxide Supported Manganese Oxide." Processes 7, no. 1 (2019): 40. http://dx.doi.org/10.3390/pr7010040.

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Graphene oxide (GO) was used as a support for manganese oxide (MnO2) for the preparation of a nanocomposite catalyst for the degradation of an azo dye, Reactive Black 5 (RB5). The nanocomposite was characterized for the structure by XRD, for the morphology with SEM, and for the surface chemistry with FTIR and potentiometric titration measurements. The GO-MnO2 nanocomposite presented a high catalytic activity for the degradation/oxidation of RB5 at ambient conditions, which was higher than that of the pure MnO2 and could be attributed to the beneficial contribution of the manganese oxide and th
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Dissertations / Theses on the topic "Oxide supported oxide"

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Burkardt, Sven. "Oxide and oxide supported nanoclusters on quasicrystals." Berlin Logos-Verl, 2009. http://d-nb.info/999419471/04.

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Shukri, Rashid Jaber Asa'd. "Supported oxide catalysts : cobalt oxide and molybdena on titania." Thesis, Brunel University, 1989. http://bura.brunel.ac.uk/handle/2438/7385.

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TiO2 supported MoO3 catalysts were prepared by aqueous impregnation of low area anatase (10 m2g-1) with solutions of (NH4)6Mo7024,4H20 (MT/C series), and H2[Mo03(C204)].H20 (MOT /C series), Three series of CoOx/Ti02 catalysts were fabricated by aqueous impregnation of the same support with solutions of Co(N03)2,6H20 (CT/C series), and Co(CH3COO)2.4H20 (CAT/C series), and by homogeneous precipitation using Co(N03)2,6H20 (CT/HP series), CoO and Mo03 were deposited on Degussa P-25 (55 m2g-1) by aqueous impregnation using (NH4)6Mo7024,4H20 and Co(N03)2,6H20 in three ways: ( i) CoO impregnated firs
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Rajan, Ziba Shabir Hussein Somjee. "Iridium oxide supported on antimony-doped tin oxide as an electrocatalyst for the oxygen evolution reaction." Master's thesis, University of Cape Town, 2020. http://hdl.handle.net/11427/32528.

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The generation of high purity hydrogen by renewable, sustainable means is a crucial building block towards the realisation of a carbon-free energy economy. Proton exchange membrane water electrolysis (PEMWE) offers a promising route for the generation of clean hydrogen, using renewable energy, for both stationary and mobile energy storage applications, and as a feedstock for the chemical industry. As water electrolysis is an electrochemical redox reaction, cathodic hydrogen evolution cannot occur without an efficient, and rapid anodic oxygen evolution reaction (OER). While both iridium and rut
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Tahir, Saad Flamerz. "Structure and reactivity of titania-supported molybdenum and vanadium oxides." Thesis, Brunel University, 1987. http://bura.brunel.ac.uk/handle/2438/7887.

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Vanadium and molybdenum oxide catalysts have been prepared on different Ti02 supports by a variety of methods. Solutions of VOC13, VO(O'Bu)3 and MoOC14 were used to graft VOX and MoOX monolayers onto the supports in a single treatment. The other methods were intended to produce more than one monolayer (i. e. aqueous impregnation and multiple treatments of VOC13 and VO(O1Bu)3 ). TPR and Raman spectroscopy showed the formation above the monolayer of a phase denoted as disordered vanadium oxide, which has the same reducibility as the monolayer species but which has a band in the Raman spectrum at
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Dhanasekaran, Venkatesan. "Oxide supported Au-Pd nanoparticles for CO oxidation reaction." Thesis, Sorbonne Paris Cité, 2017. https://theses.md.univ-paris-diderot.fr/DHANASEKARAN_Venkatesan_1_va_20170629.pdf.

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Les nanoparticules (NPs) bimétalliques Au-Pd ont été étudiées pour leur activité catalytique dans la réaction d'oxydation du CO. La technique de préparation, la taille et la composition des nanoparticules ont un grand impact sur le comportement catalytique du système. Ici, des nanoparticules de 3 et 5nm de diamètre Au1-xPdx (x = 0, 0.25, 0.5, 0.75, 1) ont été utilisées pour étudier l'effet de la taille et de la composition. Les échantillons ont été synthétisés par nano-lithographie à base de micelles, technique bien adaptée pour obtenir des particules ayant une distribution en taille étroite.
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Cheng, Lei. "FIRST-PRINCIPLES DENSITY FUNCTIONAL THEORY STUDIES OF REACTIVITIES OF HETEROGENEOUS CATALYSTS DETERMINED BY STRUCTURE AND SUBSTRATE." OpenSIUC, 2009. https://opensiuc.lib.siu.edu/dissertations/99.

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In this dissertation, density functional theory (DFT) calculations were used to investigate (1)NO2 adsorption on BaO in NOx Storage Reduction (NSR) catalyst affected by the morphology of BaO and the γ-Al2O3 support, (2) energy barrier of H2 dissociative adsorption over Mg clusters affected by its electronic structure, and (3) comparison of the activities of CeO2 clusters affected by two different supports--monoclinic ZrO2 and non-spinel γ-Al2O3. Our results showed that the electronic effect caused by the non-stoichiometry of the bare BaO clusters and surfaces improves their reactivities toward
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Xu, Chunbao. "Continuous and batch hydrothermal synthesis of metal oxide nanoparticles and metal oxide-activated carbon nanocomposites." Diss., Available online, Georgia Institute of Technology, 2006, 2006. http://etd.gatech.edu/theses/available/etd-07302006-231517/.

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Thesis (Ph. D.)--Chemical and Biomolecular Engineering, Georgia Institute of Technology, 2007.<br>Teja, Amyn, Committee Chair ; Kohl, Paul, Committee Member ; Liu, Meilin, Committee Member ; Nair,Sankar, Committee Member ; Rousseau, Ronald, Committee Member.
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Aldemir, Müge. "Metal oxide supported cadmium sulfide for photocatalytic synthesis of homoallylamines." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=978677617.

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Gnad, Christoph [Verfasser]. "Molecular Palladium Catalysts Supported on Functionalized Oxide Surfaces / Christoph Gnad." München : Verlag Dr. Hut, 2019. http://d-nb.info/1196415757/34.

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Radhakrishnan, Rakesh. "Structure and Ozone Decomposition Reactivity of Supported Manganese Oxide Catalysts." Diss., Virginia Tech, 2001. http://hdl.handle.net/10919/26033.

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Manganese oxide catalysts supported on Al2O3, ZrO2, TiO2 and SiO2 supports were used to study the effect of support on ozone decomposition kinetics. X-ray diffraction (XRD), in-situ laser Raman spectroscopy, temperature programmed oxygen desorption, surface area measurements, extended and near edge x-ray absorption fine structure (EXAFS and NEXAFS) showed that the manganese oxide was highly dispersed on the surface of the supports. EXAFS spectra suggest that the manganese active centers on all of the surfaces were surrounded by five oxygen atoms. These metal centers were of a mononuclear ty
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Books on the topic "Oxide supported oxide"

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Shukri, Rashid Jaber Asa'd. Supported oxide catalysts: Cobalt oxide and molybdena on titania. Brunel University, 1989.

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Poonsawat, Choosak. Magnesium oxide supported ethylene polymerization catalysts. UMIST, 1995.

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Zhou, Yucun. Study on Fabrication and Performance of Metal-Supported Solid Oxide Fuel Cells. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6617-7.

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O'Connor, Rodney Philip. A relationship between the amplitude and spectral characteristics of the geomagnetic field and the occurrence of sudden infant death in Canada: A possible cellular mechanism supported by a mathematical modeland experimental evidence for involvement of calcium signalling and nitric oxide. Laurentian University, Department of Biology, 2001.

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Tahir, Saad Flamerz. Structure and reactivity of titania-supported molybdenum and vanadium oxides. Brunel University, 1987.

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Żele glinowokrzemionkowe jako ligandy kompleksów tytanu i niklu. Wydawn. Politechniki Warszawskiej, 1985.

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Augugliaro, Vincenzo. Clean by light irradiation: Practical applications of supported TiO₂. Royal Society of Chemistry, 2010.

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Seeker, W. R. Fundamental combustion research applied to pollution formation, volume III: Support studies : measurement studies. U.S. Environmental Protection Agency, Air and Energy Engineering Research Laboratory, 1988.

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Zhou, Yucun. Study on Fabrication and Performance of Metal-Supported Solid Oxide Fuel Cells. Springer, 2017.

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Zhou, Yucun. Study on Fabrication and Performance of Metal-Supported Solid Oxide Fuel Cells. Springer, 2017.

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Book chapters on the topic "Oxide supported oxide"

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Bengoa, J. F., S. G. Marchetti, M. V. Cagnoli, A. M. Alvarez, N. G. Gallegos, and R. C. Mercader. "Study of Oxide-Support Interactions in Silica-Supported Iron Oxide Precursors." In Hyperfine Interactions (C). Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0281-3_119.

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Dosch, Robert G., Frances V. Stohl, and James T. Richardson. "Hydrous Titanium Oxide-Supported Catalysts." In Novel Materials in Heterogeneous Catalysis. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0437.ch026.

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Alfredsson, M., S. T. Bromley, and C. R. A. Catlow. "Modelling of Oxide-Supported Metals." In Theoretical Aspects of Heterogeneous Catalysis. Springer Netherlands, 2001. http://dx.doi.org/10.1007/0-306-47667-3_5.

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Reddy, B. Mahipal. "Structure and Reactivity of Tin Oxide-Supported Vanadium Oxide Catalysts." In ACS Symposium Series. American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1993-0523.ch015.

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Noguera, C., A. Pojani, F. Finocchi, and J. Goniakowski. "Stability of Polar Oxide Surfaces." In Chemisorption and Reactivity on Supported Clusters and Thin Films. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-015-8911-6_16.

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Franchini, Cesare, and Francesco Allegretti. "Low Dimensionality and Epitaxial Stabilization in Metal-Supported Oxide Nanostructures: Mnx Oy on Pd(100) Mnx Oy." In Functional Metal Oxide Nanostructures. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-9931-3_10.

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Larring, Yngve, and Marie-Laure Fontaine. "Critical Issues of Metal-Supported Fuel Cell." In Solid Oxide Fuels Cells: Facts and Figures. Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-4456-4_4.

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Deo, Goutam, and Israel E. Wachs. "Surface Oxide—Support Interactions in the Molecular Design of Supported Metal Oxide Selective Oxidation Catalysts." In ACS Symposium Series. American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1993-0523.ch003.

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Møller, P. J. "Co-Adsorption on Metal-Oxide Crystal Surfaces." In Chemisorption and Reactivity on Supported Clusters and Thin Films. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-015-8911-6_10.

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Yoo, Yeong, Naoki Oishi, Daniel Roth, and Suwas Nikumb. "Development of Metal Supported Thin Film SOFCs at ICPET/NRCC." In Advances in Solid Oxide Fuel Cells III. John Wiley & Sons, Inc., 2009. http://dx.doi.org/10.1002/9780470339534.ch2.

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Conference papers on the topic "Oxide supported oxide"

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Choi, Sung R., Donald J. Alexander, and Robert W. Kowalik. "Foreign Object Damage in an Oxide/Oxide Composite at Ambient Temperature." In ASME Turbo Expo 2008: Power for Land, Sea, and Air. ASMEDC, 2008. http://dx.doi.org/10.1115/gt2008-50505.

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Foreign object damage (FOD) behavior of an oxide/oxide (N720/AS) ceramic matrix composite (CMC) was determined at ambient temperature using impact velocities ranging from 100 to 400 m/s by 1.59-mm diameter steel-ball projectiles. Two different support configurations of target specimens were used: fully supported and partially supported. The degree of post-impact strength degradation increased with increasing impact velocity, and was greater in a partially supported configuration than in a fully supported one. For the fully supported configuration, frontal contact stress played a major role in
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Rout, D., R. N. Viswanath, S. Dash, and A. K. Tyagi. "Carbon supported In-Sn oxide films." In International Conference on Nanoscience, Engineering and Technology (ICONSET 2011). IEEE, 2011. http://dx.doi.org/10.1109/iconset.2011.6168017.

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Kodama, Tatsuya, Nobuki Imaizumi, Nobuyuki Gokon, Tsuyoshi Hatamachi, Daiki Aoyagi, and Ken Kondo. "Comparison Studies of Reactivity on Nickel-Ferrite and Cerium-Oxide Redox Materials for Two-Step Thermochemical Water Splitting Below 1400°C." In ASME 2011 5th International Conference on Energy Sustainability. ASMEDC, 2011. http://dx.doi.org/10.1115/es2011-54277.

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A two-step thermochemical water splitting cycle using a redox system of non-volatile metal oxide is one of the promising processes for converting concentrated solar high-temperature heat into clean hydrogen in sun-belt regions. In the 1st step of the cycle or the thermal reduction step, metal oxide is thermally reduced to release oxygen molecules in an inert gas atmosphere at a higher temperature above 1400°C. In the second step or the water-decomposition step at a lower temperature, the thermally-reduced metal oxide reacts with steam to produce hydrogen. As the reactive redox metal oxide mate
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Royer, Nathanael, Ryan Hamilton, Jeffrey Collins, John Drazin, and Dustin McLarty. "Performance of Pressurized Anode Supported Solid Oxide Fuel Cell." In ASME 2019 13th International Conference on Energy Sustainability collocated with the ASME 2019 Heat Transfer Summer Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/es2019-3912.

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Abstract A commercially available Anode Supported Cell (ASC) with an active area of 81 cm2 was characterized at pressures up to 9 bar at 750 °C using a custom-built pressurized test stand. Open Circuit Voltage (OCV) measurements of the cell indicated the existence of an intercell leak due to a cracked cell. Voltage characteristic curves were measured at 1, 3, and 9 bar using 50/50 N2/H2 (1.2 SLPM) and bottled air (1.5 SLPM). Measured current density at 0.70 V increased from 0.37 A·cm−2 to 0.43 A·cm−2 as a result of pressurization from atmospheric to 9 bar. Subsequent measurements were taken wh
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Zhang, Lingling, Xue Li, Siwei Wang, Kevin Gregory Romito, and Kevin Huang. "Synthesis of Mixed Oxide-Ion and Carbonate-Ion Conductors Supported by a Prefabricated Porous Solid Oxide Matrix." In ASME 2011 9th International Conference on Fuel Cell Science, Engineering and Technology collocated with ASME 2011 5th International Conference on Energy Sustainability. ASMEDC, 2011. http://dx.doi.org/10.1115/fuelcell2011-54076.

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A novel two-step approach is used to fabricate a two-phase mixed oxide-ion and carbonate-ion conductor (MOCC) that has been recently developed for intermediate temperature solid oxide fuel cells (IT-SOFCs) and CO2 separation membranes. In this study, a samarium doped ceria (SDC) is selected as an example to demonstrate the prefabrication of porous matrix by the “sacrificial template” methodology with NiO as the template material. NiO has been reduced into elemental Ni in the composite, and then removed by dissolving into a nitric acid. It was demonstrated by XRD, EDS and weight changes. The mi
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Sharma, Arti, Sunil Kumar, Arunendra Kumar Patel, Anil Kumar Bajpai, and Rakesh Bajpai. "Poly (vinyl alcohol) supported flexible films of graphene oxide and reduced graphene oxide and their structural study." In PROCEEDINGS OF ADVANCED MATERIAL, ENGINEERING & TECHNOLOGY. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0025343.

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Phoocharoen, Niwat, and Jarruwat Charoensuk. "Numerical Simulation of Metal-Supported Solid Oxide Fuel Cell (mSOFC)." In ASME 2009 7th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2009. http://dx.doi.org/10.1115/fuelcell2009-85017.

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In this paper we present the numerical results of planar solid oxide fuel cell at the level of membrane electrode assembly, MEA. The study is aimed at evaluating the performance of metal-supported design versus the conventional anode-cathode support under co-flow and counter-flow conditions. We have found that the value of peak temperature is lower therefore better temperature distribution is achieved for metal supported design with counter-flow configuration. Moreover the corresponding current density at maximum power is also higher with this configuration. This later design however possesses
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Jeong, Jihoon, Seung-Wook Baek, and Joongmyeon Bae. "Hydrocarbon Fueled Operation of Metal-Supported Solid Oxide Fuel Cell." In ASME 2010 8th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2010. http://dx.doi.org/10.1115/fuelcell2010-33157.

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The metal-supported solid oxide fuel cell (SOFC) was studied. Hydrocarbon fueled operation was used to make SOFC system. Different operating characteristics for metal-supported SOFC are used than for conventional ones. Metal-supported SOFC was successfully fabricated by a high temperature sinter-joining method and the cathode was in-situ sintered. Synthetic gas, which is compounded as the diesel reformate gas composition and low hydrocarbons was completely removed by the diesel reformer. Metal-supported SOFC with synthetic gas was operated and evaluated and its characteristics analyzed. The pe
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Othman, Nur Hidayati, Nur Hashimah Alias, Munawar Zaman Shahruddin, Siti Nurliyana Che Mohamed Hussein, and Aqilah Dollah. "Supported graphene oxide hollow fibre membrane for oily wastewater treatment." In ADVANCED MATERIALS FOR SUSTAINABILITY AND GROWTH: Proceedings of the 3rd Advanced Materials Conference 2016 (3rd AMC 2016). Author(s), 2017. http://dx.doi.org/10.1063/1.5010445.

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Madhavan, Jithin, Malay Kumar Das, and Ashoke De. "Lattice Boltzmann simulations of anode supported solid oxide fuel cell." In PROCEEDINGS OF THE INTERNATIONAL ENGINEERING RESEARCH CONFERENCE - 12TH EURECA 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5120207.

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Reports on the topic "Oxide supported oxide"

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Dosch, R., H. Stephens, F. Stohl, B. Bunker, and C. Peden. Hydrous metal oxide-supported catalysts. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/7015232.

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Notestein, Justin M. Templating Routes to Supported Oxide Catalysts by Design. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1322744.

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Brown, J. R. Surface chemistry and reduction behaviour of y-alumina supported molybdenum oxide. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1987. http://dx.doi.org/10.4095/304349.

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Dosch, R. G., H. P. Stephens, and F. V. Stohl. Hydrous metal oxide-supported catalysts: Part 2, Catalytic properties and applications. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/5003423.

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Bai, C. S., S. Soled, K. Dwight, and A. Wold. Preparation and Characterization of Dispersed 'Cobalt Oxide' Supported on Gamma-Al2O3. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada231269.

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Harrison, Ian. Investigation of the Origin of Catalytic Activity in Oxide-Supported Nanoparticle Gold. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1358579.

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Gardner, T. J., L. I. McLaughlin, L. R. Evans, and A. K. Datye. Preparation and evaluation of novel hydrous metal oxide (HMO)-supported noble metal catalysts. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/671938.

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Morris D. Argyle. Supported, Alkali-Promoted Cobalt Oxide Catalysts for NOx Removal from Coal Combustion Flue Gases. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/913563.

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Virkar, Anil V. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/788101.

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Prof. Anil V. Virkar. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/784599.

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