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Journal articles on the topic 'Oxide supported oxide'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Kesavan, V., D. Dhar, Y. Koltypin, et al. "Nanostructured amorphous metals, alloys, and metal oxides as new catalysts for oxidation." Pure and Applied Chemistry 73, no. 1 (2001): 85–91. http://dx.doi.org/10.1351/pac200173010085.

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The oxidation of cyclohexane with molecular oxygen in the presence of isobutyraldehyde catalyzed by nanostructured iron and cobalt oxides and iron oxide supported on titania has been studied. Nanostructured cobalt oxide on MCM-41 is found to be efficient for catalytic aerobic epoxidation of olefins.

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12

Cant, Noel W., and Michael J. Patterson. "The storage of nitrogen oxides on alumina-supported barium oxide." Catalysis Today 73, no. 3-4 (2002): 271–78. http://dx.doi.org/10.1016/s0920-5861(02)00010-x.

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13

Liu, Xiangqian, and Weihua Hu. "Iron oxide/oxyhydroxide decorated graphene oxides for oxygen reduction reaction catalysis: a comparison study." RSC Advances 6, no. 35 (2016): 29848–54. http://dx.doi.org/10.1039/c5ra28038a.

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14

Batakliev, Todor, Slavcho Rakovsky, Gennady Zaikov, Vladimir Georgiev, and Metodi Anachkov. "Catalytic Activity of Titania-Supported Manganese Oxide Catalyst in Ozone Decomposition." Vestnik Volgogradskogo gosudarstvennogo universiteta. Serija 10. Innovatcionnaia deiatel’nost’, no. 5 (November 24, 2014): 27–36. http://dx.doi.org/10.15688/jvolsu10.2014.5.3.

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15

Xamidov, Anvar, Farhodjon Hoshimov, Shavkat Mamatkulov, Khakimjan Butanov, Mirakhmat Yunusov, and Olim Ruzimuradov. "Catalytic Activity of Ni, Co, Mo Supported Anodic Aluminum Oxide Nanocomposites." Bulletin of Chemical Reaction Engineering & Catalysis 15, no. 3 (2020): 845–52. http://dx.doi.org/10.9767/bcrec.15.3.8480.845-852.

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Nanostructured catalysts based on porous aluminum oxide (PAO) and some 3d metals, such as: nickel, cobalt, and molybdenum, have been obtained by anodic oxidation and impregnation. The synthesis of porous aluminum oxide with a highly ordered pore structure with pore sizes of 50 nm and a thickness of 50 µm is carried out by the method of two-stage anodic oxidation. The catalysts are obtained by impregnation of 3d metals into nanosized pores of aluminum oxide. The obtained catalysts based on nickel and porous Al2O3 are studied by scanning electron microscopy (SEM-EDX). The results of SEM-EDX anal

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16

Cruz, Aloisio Magela de Aguilar, and Jean Guillaume Eon. "Boehmite-supported vanadium oxide catalysts." Applied Catalysis A: General 167, no. 2 (1998): 203–13. http://dx.doi.org/10.1016/s0926-860x(97)00316-5.

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17

Fisher, James C., Jak Tanthana, and Steven S. C. Chuang. "Oxide-supported tetraethylenepentamine for CO2capture." Environmental Progress & Sustainable Energy 28, no. 4 (2009): 589–98. http://dx.doi.org/10.1002/ep.10363.

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18

Kapteijn, F., A. D. Vanlangeveld, J. A. Moulijn, et al. "Alumina-Supported Manganese Oxide Catalysts." Journal of Catalysis 150, no. 1 (1994): 94–104. http://dx.doi.org/10.1006/jcat.1994.1325.

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19

Kapteijn, F., L. Singoredjo, M. Vandriel, et al. "Alumina-Supported Manganese Oxide Catalysts." Journal of Catalysis 150, no. 1 (1994): 105–16. http://dx.doi.org/10.1006/jcat.1994.1326.

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20

Sasaki, K., Z. Noda, T. Tsukatsune, et al. "Alternative Oxide-Supported PEFC Electrocatalysts." ECS Transactions 64, no. 3 (2014): 221–27. http://dx.doi.org/10.1149/06403.0221ecst.

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21

HINO, M., and K. ARATA. "ChemInform Abstract: Superacids by Metal Oxides. Part 5. Synthesis of Highly Acidic Catalysts of Tungsten Oxide Supported on Tin Oxide, Titanium Oxide, and Iron Oxide." ChemInform 25, no. 39 (2010): no. http://dx.doi.org/10.1002/chin.199439048.

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22

Antol, Marcel, Katarina Prandová, and Milan Hronec. "Promoted TiO2 (Anatase)-Supported Vanadium Oxide Catalysts. TPR Study and Activity in Oxidation of Toluene." Collection of Czechoslovak Chemical Communications 61, no. 11 (1996): 1665–74. http://dx.doi.org/10.1135/cccc19961665.

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Vanadium oxide doped with K, Li, Bi, Sb, Te, U or Mo oxide, supported on TiO2 - anatase, was studied by temperature programmed reduction (TPR). The influence of the addition of promoters (up to molar ratio M : V = 0.5) to 5 wt.% V2O5/TiO2 catalyst on the TPR profile is presented in correlation with their catalytic activity in the vapor phase oxidation of toluene. All promoters, except Bi2O3, decrease the catalyst reducibility and decrease the rate of the toluene oxidation. A strong negative influence on the activity of the toluene oxidation have K, Li, and Te oxides. However, the presence of a

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23

Baltes, Michael, Arla Kytökivi, Bert M. Weckhuysen, Robert A. Schoonheydt, Pascal Van Der Voort, and Etienne F. Vansant. "Supported Tantalum Oxide and Supported Vanadia-tantala Mixed Oxides: Structural Characterization and Surface Properties." Journal of Physical Chemistry B 105, no. 26 (2001): 6211–20. http://dx.doi.org/10.1021/jp010628b.

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24

Hino, Makoto, and Kazushi Arata. "Synthesis of Highly Acidic Catalysts of Tungsten Oxide Supported on Tin Oxide, Titanium Oxide, and Iron Oxide." Bulletin of the Chemical Society of Japan 67, no. 5 (1994): 1472–74. http://dx.doi.org/10.1246/bcsj.67.1472.

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25

Huang, Haiping, Lianlian Lv, Zhongzhen Chen, Yanan Chen, Yongmei Hu, and Fang Xu. "Dysprosium Oxide-Graphene Oxide Supported Hemoglobin for Biosensing of H2O2." Chemistry Letters 48, no. 2 (2019): 114–17. http://dx.doi.org/10.1246/cl.180782.

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26

Liu, Yan, Xiaojun Zhang, Meiyan Yang, Bowen Guo, Jixiang Guo, and Dan Luo. "Three-Dimensional Graphene Oxide-Supported Zinc Oxide Scaffold as a High-Efficiency Adsorbent for Desulfurization." Nano 15, no. 05 (2020): 2050059. http://dx.doi.org/10.1142/s1793292020500599.

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Sulfur oxides are air pollutants derived mainly from the combustion of gasoline. Reducing the sulfur content of fluid catalytic cracking (FCC) gasoline is of key importance for the prevention and control of atmospheric pollution. We describe herein the fabrication and characterization of a porous, three-dimensional (3D) graphene oxide-supported zinc oxide (GO/ZnO) scaffold as an adsorbent for desulfurization with various model compounds and real FCC gasoline. The uniform and stable dispersion of ZnO nanoparticles on the surface of GO facilitates the specific binding of sulfides. Moreover, GO s

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27

Elmacı, Gökhan, Carolin E. Frey, Philipp Kurz, and Birgül Zümreoğlu-Karan. "Water oxidation catalysis by using nano-manganese ferrite supported 1D-(tunnelled), 2D-(layered) and 3D-(spinel) manganese oxides." Journal of Materials Chemistry A 4, no. 22 (2016): 8812–21. http://dx.doi.org/10.1039/c6ta00593d.

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28

KÖSE, Hilal, Şeyma DOMBAYCIOĞLU, Hatem AKBULUT, and Ali Osman AYDIN. "Reduced graphene oxide supported tin oxide-boron oxide flexible paper anodesfor Li-ion batteries." TURKISH JOURNAL OF CHEMISTRY 43, no. 5 (2019): 1244–57. http://dx.doi.org/10.3906/kim-1904-6.

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29

Zhang, G., E. I. Papaioannou, and I. S. Metcalfe. "Selective, high-temperature permeation of nitrogen oxides using a supported molten salt membrane." Energy & Environmental Science 8, no. 4 (2015): 1220–23. http://dx.doi.org/10.1039/c4ee02256d.

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Nitrate/ceramic membranes were designed for selective nitrogen oxide permeation. These membranes exhibited selective permeation of nitrogen oxides over carbon dioxide and could be employed in e.g. sensing technologies.

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30

Hinokuma, Satoshi, Shun Matsuki, Yusuke Kawabata, Hiroki Shimanoe, Saaya Kiritoshi, and Masato Machida. "Copper Oxides Supported on Aluminum Oxide Borates for Catalytic Ammonia Combustion." Journal of Physical Chemistry C 120, no. 43 (2016): 24734–42. http://dx.doi.org/10.1021/acs.jpcc.6b07157.

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31

Petre, A. L., J. A. Perdigón-Melón, A. Gervasini, and A. Auroux. "Characterization and reactivity of group III oxides supported on niobium oxide." Catalysis Today 78, no. 1-4 (2003): 377–86. http://dx.doi.org/10.1016/s0920-5861(02)00300-0.

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32

Iruretagoyena, Diana, Milo S. P. Shaffer, and David Chadwick. "Adsorption of carbon dioxide on graphene oxide supported layered double oxides." Adsorption 20, no. 2-3 (2013): 321–30. http://dx.doi.org/10.1007/s10450-013-9595-3.

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33

Zhang, Shengming, Xuhui Wang, Yan Li, et al. "Facile synthesis of carbon nanotube-supported NiO//Fe2O3 for all-solid-state supercapacitors." Beilstein Journal of Nanotechnology 10 (September 23, 2019): 1923–32. http://dx.doi.org/10.3762/bjnano.10.188.

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We have successfully prepared iron oxide and nickel oxide on carbon nanotubes on carbon cloth for the use in supercapacitors via a simple aqueous reduction method. The obtained carbon cloth–carbon nanotube@metal oxide (CC-CNT@MO) three-dimensional structures combine the high specific capacitance and rich redox sites of metal oxides with the large specific area and high electrical conductivity of carbon nanotubes. The prepared CC-CNT@Fe2O3 anode reaches a high capacity of 226 mAh·g−1 at 2 A·g−1 with a capacitance retention of 40% at 40 A·g−1. The obtained CC-CNT@NiO cathode exhibits a high capa

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34

Ramis, G., Yi Li, G. Busca, et al. "Characterization of MoO3-P2O5-ZrO2 catalysts: an oxide-supported mixed oxide." Materials Chemistry and Physics 55, no. 3 (1998): 173–87. http://dx.doi.org/10.1016/s0254-0584(99)80000-5.

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35

Wang, Fey-long, and Yi-hsuan Lin. "Alkylation of Acetaldehyde with Methanol over Titanium Oxide-supported Vanadium Oxide." Chemistry Letters 21, no. 9 (1992): 1867–68. http://dx.doi.org/10.1246/cl.1992.1867.

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36

Lai, F. S., and B. C. Gates. "Nanoclusters of Iridium Oxide and of Rhodium Oxide Supported on MgO." Nano Letters 1, no. 11 (2001): 583–87. http://dx.doi.org/10.1021/nl0155882.

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37

Reddy, B. Mahipal, B. Manohar, and E. Padmanabha Reddy. "Oxygen chemisorption on titania-zirconia mixed oxide supported vanadium oxide catalysts." Langmuir 9, no. 7 (1993): 1781–85. http://dx.doi.org/10.1021/la00031a028.

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38

Zhao, Tiansheng, Yizhuo Han, and Yuhan Sun. "Cycloaddition between propylene oxide and CO2 over metal oxide supported KI." Physical Chemistry Chemical Physics 1, no. 12 (1999): 3047–51. http://dx.doi.org/10.1039/a901943j.

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39

Zieliński, Jerzy. "Reductibility of silica supported nickel oxide." Catalysis Letters 31, no. 1 (1995): 47–56. http://dx.doi.org/10.1007/bf00817032.

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40

Datye, A. K., S. Srinivasan, L. F. Allard, C. H. F. Peden, J. R. Brenner, and L. T. Thompson. "Oxide Supported MoS2Catalysts of Unusual Morphology." Journal of Catalysis 158, no. 1 (1996): 205–16. http://dx.doi.org/10.1006/jcat.1996.0020.

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41

Villarreal, I., C. Jacobson, A. Leming, Y. Matus, S. Visco, and L. De Jonghe. "Metal-Supported Solid Oxide Fuel Cells." Electrochemical and Solid-State Letters 6, no. 9 (2003): A178. http://dx.doi.org/10.1149/1.1592372.

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42

SRINIVASAN, S. "The morphology of oxide-supported MOS2." Journal of Catalysis 137, no. 2 (1992): 513–22. http://dx.doi.org/10.1016/0021-9517(92)90179-l.

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43

Feng, Z., M. E. McBriarty, A. U. Mane та ін. "Redox-driven atomic-scale changes in mixed catalysts: VOX/WOX/α-TiO2 (110)". RSC Adv. 4, № 110 (2014): 64608–16. http://dx.doi.org/10.1039/c4ra14140g.

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X-ray study of vanadium–tungsten mixed-monolayer-oxide catalysts grown on the rutile α-TiO<sub>2</sub> (110) single crystal surface shows redox behavior not observed for lone supported vanadium or tungsten oxides.

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44

Wachs, Israel E. "Raman and IR studies of surface metal oxide species on oxide supports: Supported metal oxide catalysts." Catalysis Today 27, no. 3-4 (1996): 437–55. http://dx.doi.org/10.1016/0920-5861(95)00203-0.

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45

Reddy, Benjaram M., Ibram Ganesh, and Biswajit Chowdhury. "Design of stable and reactive vanadium oxide catalysts supported on binary oxides." Catalysis Today 49, no. 1-3 (1999): 115–21. http://dx.doi.org/10.1016/s0920-5861(98)00415-5.

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46

Bonne, R. L. C., A. D. Vanlangeveld, and J. A. Moulijn. "Temperature-Programmed Sulfiding of Vanadium Oxides and Alumina-Supported Vanadium Oxide Catalysts." Journal of Catalysis 154, no. 1 (1995): 115–23. http://dx.doi.org/10.1006/jcat.1995.1153.

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47

Spasova, I., P. Nikolov, and D. Mehandjiev. "Adsorption of NO on alumina-supported oxides and oxide–hydroxides of manganese." Journal of Colloid and Interface Science 290, no. 2 (2005): 343–49. http://dx.doi.org/10.1016/j.jcis.2005.04.043.

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48

Jo, Jin-Oh, Quang Hung Trinh, Seong H. Kim та Young Sun Mok. "Plasma-catalytic decomposition of nitrous oxide over γ-alumina-supported metal oxides". Catalysis Today 310 (липень 2018): 42–48. http://dx.doi.org/10.1016/j.cattod.2017.05.028.

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49

Guerrero-Torres, Antonio, Carmen Jiménez-Gómez, Juan Cecilia, et al. "Influence of the Incorporation of Basic or Amphoteric Oxides on the Performance of Cu-Based Catalysts Supported on Sepiolite in Furfural Hydrogenation." Catalysts 9, no. 4 (2019): 315. http://dx.doi.org/10.3390/catal9040315.

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Cu-based catalysts supported on sepiolite have been tested in vapor-phase hydrogenation of furfural. The incorporation of basic or amphoteric metal oxides (magnesium oxide, zinc oxide, or cerium oxide) improves the catalytic behavior, reaching a maximum furfural conversion above 80% after 5 h of reaction at 210 °C. In all cases, the main product is furfuryl alcohol, obtaining 2-methylfuran in lower proportions. The incorporation of these metal oxide species ameliorates the dispersion of metallic Cu nanoparticles, increasing the number of available Cu0-sites, which enhances the catalytic perfor

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50

Miller, Joel B., Stephen J. DeCanio, John B. Michel, and Cecil Dybowski. "Magnetic resonance study of titanium(IV) oxide, vanadium(V) oxide/titanium(IV) oxide, and vanadium(V) oxide supported rhodium catalysts." Journal of Physical Chemistry 89, no. 12 (1985): 2592–96. http://dx.doi.org/10.1021/j100258a033.

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