Preparation of Au and Au-Ce Catalysts Supported on Acid-Activated Bentontie and its Catalytic Performance

2011 ◽  
Vol 287-290 ◽  
pp. 1704-1707
Author(s):  
Rong Bin Zhang ◽  
Liu Jing Yao ◽  
Yan Ju
Keyword(s):  
Catalytic Activity ◽  
Co Oxidation ◽  
Surface Area ◽  
Pore Volume ◽  
Catalytic Performance ◽  
Substantial Improvement ◽  
Au Catalyst ◽  
Activated Bentonite

Acid-activated by H2SO4was applied to modify bentonite. Acid-activated bentonite supported Au catalyst was prepared by deposition-precipitation and compared with SiO2supported one. CTAB was used to modify the surface of acid-activated bentonite. Au-Ce/bentontie catalyst was prepared by adding Ce into catalyst as assistant. CO oxidation was used to evaluate the catalytic activity of samples. These samples were characterized by BET, XRD, ICP and CO-TPD. The activity results showed that Au/Bentonite was more active than Au/SiO2. The BET results showed that the surface area and pore volume of acid-activated bentontie had a substantial improvement. Using the bentontie acid-activated by 30wt%H2SO4as supporter，the Au-Ce catalyst has a better catalytic performance than Au catalyst.

scholarly journals Surface and Catalytic Properties of γ-Irradiated Cr2O3/Al2O3 Solids

1997 ◽  
Vol 15 (6) ◽  
pp. 465-476 ◽  
Author(s):  
G.A. El-Shobaky ◽  
A.M. Ghozza ◽  
G.M. Mohamed
Keyword(s):  
Catalytic Activity ◽  
Co Oxidation ◽  
Surface Area ◽  
Pore Volume ◽  
Active Sites ◽  
Catalytic Properties ◽  
Total Pore Volume ◽  
Bet Surface Area ◽  
Two Samples ◽  
Γ Rays

Two samples of Cr2O3/Al2O3 were prepared by mixing a known mass of finely powdered Al(OH)3 with a calculated amount of CrO3 solid followed by drying at 120°C and calcination at 400°C. The amounts of chromium oxide employed were 5.66 and 20 mol% Cr2O3, respectively. The calcined solid specimens were then treated with different doses of γ-rays (20–160 Mrad). The surface and catalytic properties of the different irradiated solids were investigated using nitrogen adsorption at −196°C and the catalysis of CO oxidation by O2 at 300–400°C. The results revealed that γ-rays brought about a slight decrease in the BET surface area, SBET (15%), and in the total pore volume, Vp (20%), of the adsorbent containing 5.66 mol% Cr2O3. The same treatment increased the total pore volume, Vp (36%), and the mean pore radius, r̄ (43%), of the other adsorbent sample without changing its BET surface area. The catalytic activities of both catalyst samples were found to increase as a function of dose, reaching a maximum value at 80–160 Mrad and 40 Mrad for the solids containing 5.66 and 20 mol% Cr2O3, respectively. The maximum increase in the catalytic activity measured at 300°C was 59% and 100% for the first and second catalyst samples, respectively. The induced effect of γ-irradiation on the catalytic activity was an increase in the concentration of catalytically active sites taking part in chemisorption and in the catalysis of CO oxidation by O2 without changing their energetic nature. This was achieved by a progressive removal of surface hydroxy groups during the irradiation process.

scholarly journals Influence of the Reduction Temperature and the Nature of the Support on the Performance of Zirconia and Alumina-Supported Pt Catalysts for n-Dodecane Hydroisomerization

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 88
Author(s):  
Diana García-Pérez ◽  
Maria Consuelo Alvarez-Galvan ◽  
Jose M. Campos-Martin ◽  
Jose L. G. Fierro
Keyword(s):  
Catalytic Activity ◽  
Surface Area ◽  
Catalytic Properties ◽  
Catalytic Performance ◽  
Major Influence ◽  
Pt Catalysts ◽  
Reduction Temperature ◽  
Metal Dispersion ◽  
Tungsten Oxides ◽  
Supported Pt Catalysts

Catalysts based on zirconia- and alumina-supported tungsten oxides (15 wt % W) with a small loading of platinum (0.3 wt % Pt) were selected to study the influence of the reduction temperature and the nature of the support on the hydroisomerization of n-dodecane. The reduction temperature has a major influence on metal dispersion, which impacts the catalytic activity. In addition, alumina and zirconia supports show different catalytic properties (mainly acid site strength and surface area), which play an important role in the conversion. The NH3-TPD profiles indicate that the acidity in alumina-based catalysts is clearly higher than that in their zirconia counterparts; this acidity can be attributed to a stronger interaction of the WOx species with alumina. The PtW/Al catalyst was found to exhibit the best catalytic performance for the hydroisomerization of n-dodecane based on its higher acidity, which was ascribed to its larger surface area relative to that of its zirconia counterparts. The selectivity for different hydrocarbons (C7–10, C11 and i-C12) was very similar for all the catalysts studied, with branched C12 hydrocarbons being the main products obtained (~80%). The temperature of 350 °C was clearly the best reduction temperature for all the catalysts studied in a trickled-bed-mode reactor.

scholarly journals On the Effects of Doping on the Catalytic Performance of (La,Sr)CoO3. A DFT Study of CO Oxidation

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 312 ◽  
Author(s):  
Antonella Glisenti ◽  
Andrea Vittadini
Keyword(s):  
Catalytic Activity ◽  
Co Oxidation ◽  
Density Functional Calculations ◽  
Density Functional ◽  
Formation Energy ◽  
Oxygen Vacancies ◽  
Catalytic Performance ◽  
Energy Profiles ◽  
High Concentrations ◽  
3D Impurities

The effects of modifying the composition of LaCoO3 on the catalytic activity are predicted by density functional calculations. Partially replacing La by Sr ions has benefical effects, causing a lowering of the formation energy of O vacancies. In contrast to that, doping at the Co site is less effective, as only 3d impurities heavier than Co are able to stabilize vacancies at high concentrations. The comparison of the energy profiles for CO oxidation of undoped and of Ni-, Cu-m and Zn-doped (La,Sr)CoO3(100) surface shows that Cu is most effective. However, the effects are less spectacular than in the SrTiO3 case, due to the different energetics for the formation of oxygen vacancies in the two hosts.

A mesoporous “shell-in-shell” structured nanocatalyst with large surface area, enhanced synergy, and improved catalytic performance for Suzuki–Miyaura coupling reaction

2014 ◽  
Vol 50 (82) ◽  
pp. 12356-12359 ◽  
Author(s):  
Baocang Liu ◽  
Yuefang Niu ◽  
Yan Li ◽  
Fan Yang ◽  
Jiamin Guo ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Surface Area ◽  
Coupling Reaction ◽  
Catalytic Performance ◽  
Large Surface Area ◽  
Mesoporous Shell

A novel mesoporous “shell-in-shell” structured nanoreactor (@Pd/meso-TiO2/Pd@meso-SiO2) shows superior catalytic activity, stability, and selectivity for Suzuki–Miyaura coupling reaction.

scholarly journals Metal Nanoparticles as Green Catalysts

Materials ◽  
2019 ◽  
Vol 12 (21) ◽  
pp. 3602 ◽  
Author(s):  
Neel Narayan ◽  
Ashokkumar Meiyazhagan ◽  
Robert Vajtai
Keyword(s):  
Catalytic Activity ◽  
Composite Materials ◽  
Green Synthesis ◽  
Metal Nanoparticles ◽  
Surface Area ◽  
Significant Role ◽  
High Surface ◽  
High Surface Area ◽  
Catalytic Performance ◽  
Materials Development

Nanoparticles play a significant role in various fields ranging from electronics to composite materials development. Among them, metal nanoparticles have attracted much attention in recent decades due to their high surface area, selectivity, tunable morphologies, and remarkable catalytic activity. In this review, we discuss various possibilities for the synthesis of different metal nanoparticles; specifically, we address some of the green synthesis approaches. In the second part of the paper, we review the catalytic performance of the most commonly used metal nanoparticles and we explore a few roadblocks to the commercialization of the developed metal nanoparticles as efficient catalysts.

scholarly journals Pembuatan Katalis Pd-Ce/γ –Al2O3 dan Uji Aktivitas terhadap Oksidasi Metana

1999 ◽  
Vol 2 (3) ◽  
pp. 104-111
Author(s):  
Ahmad Suseno ◽  
Triyono Triyono ◽  
Bambang Setiaji
Keyword(s):  
Catalytic Activity ◽  
Surface Area ◽  
Pore Volume ◽  
Pore Radius ◽  
Flow Reactor ◽  
Chloride Salt ◽  
Oxidation Of Methane ◽  
Sorption Method ◽  
Determine Surface Area ◽  
Products Of Reaction

Effects of Ce addition on Pt/γ - Al2O3 catalysts preparation and their catalytic activity on oxidation of methane have been investigated. In this study, the catalysts were prepared by impregnating chloride salt solution of palladium and sulphate salt of cerium on γ-AI2O3 support. Characterization of catalysts was conducted by gas sorption method to determine surface area, pore radius and pore volume. The test of catalytic activity on oxidation of methane was carried out in a flow reactor system at a temperature range from 350°C to 600°C. Products of reaction were analysed by non-dispersive IR spectroscopy. It was observed that the surface area, pore radius and pore volume decrease with the addition of cerium. The results of oxidation process showed that Pd-Ce/γ-Al2O3 catalyst can be used for oxidation of methane up to 90.62% conversion

Large-scale and facile synthesis of a porous high-entropy alloy CrMnFeCoNi as an efficient catalyst

2020 ◽  
Vol 8 (35) ◽  
pp. 18318-18326 ◽  
Author(s):  
Hailong Peng ◽  
Yangcenzi Xie ◽  
Zicheng Xie ◽  
Yunfeng Wu ◽  
Wenkun Zhu ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Surface Area ◽  
Large Scale ◽  
High Surface ◽  
High Surface Area ◽  
Catalytic Performance ◽  
High Entropy Alloy ◽  
Facile Synthesis ◽  
Efficient Catalyst ◽  
High Entropy

Porous high entropy alloy CrMnFeCoNi exhibited remarkable catalytic activity and stability toward p-nitrophenol hydrogenation. The enhanced catalytic performance not only resulted from the high surface area, but also from exposed high-index facets with terraces.

scholarly journals Catalytic activity of nanostructured Au: Scale effects versus bimetallic/bifunctional effects in low-temperature CO oxidation on nanoporous Au

2013 ◽  
Vol 4 ◽  
pp. 111-128 ◽  
Author(s):  
Lu-Cun Wang ◽  
Yi Zhong ◽  
Haijun Jin ◽  
Daniel Widmann ◽  
Jörg Weissmüller ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Low Temperature ◽  
Co Oxidation ◽  
Surface Area ◽  
Photoelectron Spectroscopy ◽  
Scale Effects ◽  
Structural Parameters ◽  
Kinetic Measurements ◽  
X Ray ◽  
Low Temperature Co Oxidation

The catalytic properties of nanostructured Au and their physical origin were investigated by using the low-temperature CO oxidation as a test reaction. In order to distinguish between structural effects (structure–activity correlations) and bimetallic/bifunctional effects, unsupported nanoporous gold (NPG) samples prepared from different Au alloys (AuAg, AuCu) by selective leaching of a less noble metal (Ag, Cu) were employed, whose structure (surface area, ligament size) as well as their residual amount of the second metal were systematically varied by applying different potentials for dealloying. The structural and chemical properties before and after 1000 min reaction were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The catalytic behavior was evaluated by kinetic measurements in a conventional microreactor and by dynamic measurements in a temporal analysis of products (TAP) reactor. The data reveal a clear influence of the surface contents of residual Ag and Cu species on both O2 activation and catalytic activity, while correlations between activity and structural parameters such as surface area or ligament/crystallite size are less evident. Consequences for the mechanistic understanding and the role of the nanostructure in these NPG catalysts are discussed.

scholarly journals Properties and catalytic performance of sulphate-vanadia impregnated fumed silica as oxidative catalyst

2015 ◽  
Vol 11 (2) ◽  
Author(s):  
Nor Masdiana Zulkeple ◽  
Norhasyimah Mohd Kamal ◽  
Jamilah Mohd Ekhsan ◽  
Salasiah Che Me ◽  
Swee Ean Lim ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Charge Transfer ◽  
Surface Area ◽  
Sulphuric Acid ◽  
Fumed Silica ◽  
Catalytic Performance ◽  
Support Surface ◽  
High Catalytic Activity ◽  
Impregnation Method

A series of sulphate-vanadia impregnated fumed silica oxidative catalysts were synthesized via impregnation method. The samples were prepared by impregnation of 1 wt% of vanadium and 0.2 M of sulphuric acid onto fumed silica as support. Surface area of the silica supported samples were similar of 118 m2/g. UV-Vis DRS results showed existence of o supported V species and the charge transfer bands associated with O2- to V5+ in tetrahedral environments. Catalytic performance were evaluated via epoxidation of 1-octene to 1,2-epoxyoctane using hydrogen peroxide as an oxidant. It had been demonstrated that sulphate-vanadia impregnated fumed silica had high catalytic activity of 626 ± 0.2 mmol epoxide was produced after 24 h reaction. This may indicate that more oxidative sites were generated after the impregnation of V and sulphate onto the SiO2 matrixes.

High-heat treatment enhanced catalytic activity of CuO/CeO2 catalysts with low CuO content for CO oxidation

2020 ◽  
Vol 10 (15) ◽  
pp. 5256-5266 ◽  
Author(s):  
Jihang Yu ◽  
Qiangsheng Guo ◽  
Xiuzhen Xiao ◽  
Haifang Mao ◽  
Dongsen Mao ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Catalytic Activity ◽  
Co Oxidation ◽  
Active Sites ◽  
High Heat ◽  
Catalytic Performance

CuO/CeO2 catalysts with low CuO content and calcined at 800 °C exhibited better catalytic performance than those calcined at 500 °C. The coordinatively unsaturated copper atoms were proved to be the main active sites in the CuO/CeO2 catalysts.

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