Effect of CNTs Support Diameter on Pt Particles Size and Distribution

2007 ◽  
Vol 119 ◽  
pp. 231-234
Author(s):  
Yong Hwan Kim ◽  
Yon Ki Seo ◽  
Young Rae Cho ◽  
Kwang Ho Kim ◽  
Won Sub Chung
Keyword(s):  
Electrochemical Impedance ◽  
Pt Catalyst ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
Optimum Diameter ◽  
Electro Oxidation ◽  
Average Size ◽  
Wet Impregnation Method ◽  
Xrd And Tem ◽  
Supported Pt Catalyst

The Platinum catalysts on the carbon nanotubes(CNTs) supports of various diameters were prepared by wet impregnation method using H2PtCl6 precursor. The samples using 100nm, 15~20nm, 10~15nm and 5~10nm diameters of CNTs and carbon nanofibers(CNFs) are named Pt/t- CNFs, Pt/MWNTs20, Pt/MWNTs10 and Pt/MWNTs5, respectively. The effects of CNTs diameter on the Pt particle size and distribution were investigated by the means of powder XRD and TEM observation. In addition, the electro-catalytic characteristics for methanol electro-oxidation were estimated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) techniques. The average size of Pt particles increases as follows; Pt/MWNTs10 < Pt/MWNTs5 < Pt/MWNTs20 < Pt/t-CNFs. The electro-catalytic characteristics of Pt/MWNTs10 and Pt/MWNTs20 are found to be superior in comparison with the others. For preparation of the most effective supported Pt catalyst, the optimum diameter of CNTs support in the range of 10-20nm, is needed.

Atomic-dispersed platinum anchored on porous alumina sheets as an efficient catalyst for diboration of alkynes

2020 ◽  
Vol 56 (21) ◽  
pp. 3127-3130 ◽  
Author(s):  
Huishan Shang ◽  
Wenxing Chen ◽  
Zhuoli Jiang ◽  
Danni Zhou ◽  
Jiatao Zhang
Keyword(s):  
Porous Alumina ◽  
Pt Catalyst ◽  
Impregnation Method ◽  
Efficient Catalyst ◽  
Wet Impregnation ◽  
Highly Active ◽  
Catalytic Sites ◽  
Wet Impregnation Method

An atomic-dispersed Pt catalyst (Pt/dp-Al2O3) was fabricated via a simple wet impregnation method and demonstrated to be highly active and stable for the diboration of phenylacetylene, which is due to Pt/dp-Al2O3 providing unique catalytic sites.

scholarly journals Electro-Oxidation of Ammonia at Novel Ag2O−PrO2/γ-Al2O3 Catalysts

Coatings ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 257
Author(s):  
Mariam Khan ◽  
Naveed Kausar Janjua ◽  
Safia Khan ◽  
Ibrahim Qazi ◽  
Shafaqat Ali ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Electrochemical Impedance ◽  
Precipitation Method ◽  
Impregnation Method ◽  
X Rays ◽  
Kinetic And Thermodynamic Parameters ◽  
Catalytic Support ◽  
Transmission Electron ◽  
Electro Oxidation ◽  
Oxidation Of Ammonia

An Ag2O(x)−PrO2(y)/γ-Al2O3 electrocatalyst series (X:Y is for Ag:Pr from 0 to 10) was synthesized, to use synthesized samples in electrochemical applications, a step in fuel cells advancements. Ag2O(x)−PrO2(y)/γ-Al2O3/Glassy-Carbon was investigated for electrochemical oxidation of ammonia in alkaline medium and proved to be highly effective, having high potential utility, as compared to commonly used Pt-based electrocatalysts. In this study, gamma alumina as catalytic support was synthesized via precipitation method, and stoichiometric wt/wt.% compositions of Ag2O−PrO2 were loaded on γ-Al2O3 by co-impregnation method. The desired phase of γ-Al2O3 and supported nanocatalysts was obtained after heat treatment at 800 and 600 °C, respectively. The successful loadings of Ag2O−PrO2 nanocatalysts on surface of γ-Al2O3 was determined by X-rays diffraction (XRD), Fourier-transform Infrared Spectroscopy (FTIR), and energy dispersive analysis (EDX). The nano-sized domain of the sample powders sustained with particle sizes was calculated via XRD and scanning electron microscopy (SEM). The surface morphology and elemental compositions were examined by SEM, transmission electron microscopy (TEM) and EDX. The conductive and electron-transferring nature was investigated by cyclic voltammetry and electrochemical impedance (EIS). Cyclic voltammetric profiles were observed, and respective kinetic and thermodynamic parameters were calculated, which showed that these synthesized materials are potential catalysts for ammonia electro-oxidation. Ag2O(6)−PrO2(4)/γ-Al2O3 proved to be the most proficient catalyst among all the members of the series, having greater diffusion coefficient, heterogeneous rate constant and lesser Gibbs free energy for this system. The catalytic activity of these electrocatalysts is revealed from electrochemical studies which reflected their potentiality as electrode material in direct ammonia fuel cell technology for energy production.

scholarly journals Nickel-based perovskite catalysts: synthesis and catalytic tests in the production of syngas

Cerâmica ◽  
2018 ◽  
Vol 64 (371) ◽  
pp. 436-442 ◽  
Author(s):  
E. O. Moraes Júnior ◽  
J. O. Leite ◽  
A. G. Santos ◽  
M. J. B. Souza ◽  
A. M. Garrido Pedrosa
Keyword(s):  
Impregnation Method ◽  
X Ray Diffraction ◽  
Organic Precursor ◽  
Wet Impregnation ◽  
Partial Oxidation Reaction ◽  
Conversion Level ◽  
Temperature Programmed ◽  
Perovskite Type ◽  
Wet Impregnation Method ◽  
H2 Selectivity

Abstract La1-xSrxNiO3 (x= 0.0, 0.3 or 0.7) perovskite-type oxides were synthesized using the modified proteic gel method and using collagen as an organic precursor. Catalysts of La1-xSrxNiO3/Al2O3 were obtained using the wet impregnation method. The synthesized catalysts were characterized by X-ray diffraction, surface area and temperature-programmed reduction. The catalysts were evaluated in the partial oxidation reaction of methane, and the levels of selectivity to CO, CO2, H2 and H2O were determined. Among the catalysts studied, the catalyst LaNiO3/Al2O3 had the highest methane conversion level (78%) and higher H2 selectivity (55%).

scholarly journals Catalytic Activity Of Cu/η-Al2O3 Catalysts Prepared From Aluminum Scraps In The NH3-SCO and in the NH3-SCR of NO

2021 ◽  
Author(s):  
Nawel Jr ◽  
Thabet Makhlouf ◽  
Gerard Delahay ◽  
Hassib Tounsi
Keyword(s):  
Catalytic Oxidation ◽  
Catalytic Reduction ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
Reduction Of No ◽  
Evaporation Method ◽  
Nh3 Scr ◽  
Scr Of No ◽  
Selective Catalytic Oxidation ◽  
Wet Impregnation Method

Abstract Copper loaded η-alumina catalysts with different copper contents have been prepared by impregnation/evaporation method. The catalysts were characterized by XRD, FTIR, BET, UV–vis, H2-TPR and evaluated in the selective catalytic reduction of NO by NH3 and in the selective catalytic oxidation of NH3. The characterization techniques showed that the impregnation/evaporation method permits to obtain highly dispersed copper oxide species on the η-alumina surface when low amount of copper is used (1wt. % and 2 wt.%). The wet impregnation method made it possible to reach a well dispersion of the copper species on the surface of the alumina for the low copper contents Cu(1)-Al2O3 and Cu(2)-Al2O3. The latter justifies the similar behavior of Cu(1)-Al2O3) and Cu(2)-Al2O3 in the selective catalytic oxidation of NH3 where these catalysts exhibit a conversion of NH3 to N2 of the order of 100% at T > 500°C.

Preparation of Cr Metal Supported on Sulfated Zirconia Catalyst

2019 ◽  
Vol 948 ◽  
pp. 221-227
Author(s):  
Latifah Hauli ◽  
Karna Wijaya ◽  
Ria Armunanto
Keyword(s):  
Sulfated Zirconia ◽  
Reduction Process ◽  
Catalyst Preparation ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
Zirconia Catalyst ◽  
Isotherm Adsorption ◽  
Sulfated Zirconia Catalyst ◽  
Adsorption Desorption ◽  
Wet Impregnation Method

Catalyst of Chromium (Cr) metal supported on sulfated zirconia (SZ) was prepared by wet impregnation method. This study aim to determine the optimal concentration of Cr metal that impregnated on SZ catalyst. Preparation of catalyst was conducted at different concentrations of Cr metal (0.5%, 1%, 1.5% (w/w)), impregnated on SZ catalyst, then followed by the calcinationand reduction process. Catalysts were charaterized by FTIR, XRD, XRF, SAA, TEM, and acidity test. The results showed the Cr/SZ 1% had the highest acidity value of 8.22 mmol/g which confirmed from FTIR spectra. All the crystal phase of these catalysts were in monoclinic. The specific surface area increased with the increasing of Cr metal concentration on SZ catalyst and the isotherm adsorption-desorption of N2 gas observed all the catalysts as mesoporous material. The impregnation process formed particles agglomeration.

scholarly journals {CeO2/Bi2Mo1−xRuxO6} and {Au/Bi2Mo1−xRuxO6} Catalysts for Low-Temperature CO Oxidation

Catalysts ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 947 ◽  
Author(s):  
Edson Edain González ◽  
Ricardo Rangel ◽  
Javier Lara ◽  
Pascual Bartolo-Pérez ◽  
Juan José Alvarado-Gil ◽  
...  
Keyword(s):  
Co Oxidation ◽  
Photoelectron Spectroscopy ◽  
Supported Catalysts ◽  
Pollutant Emissions ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
X Ray ◽  
Low Temperature Co Oxidation ◽  
Carbon Dioxide Co2 ◽  
Wet Impregnation Method

Nowadays, one of the most important challenges that humanity faces is to find alternative ways of reducing pollutant emissions. CeO2/Bi2Mo1−xRuxO6 and Au/Bi2Mo1−xRuxO6 catalysts were prepared to efficiently transform carbon monoxide (CO) to carbon dioxide (CO2) at low temperatures. The systems were prepared in a two-step process. First, Bi2Mo1−xRuxO6 supports were synthesized through the hydrothermal procedure under microwave heating. Then, CeO2 was deposited on Bi2Mo1−xRuxO6 using the wet impregnation method, while the incipient impregnation method was selected to deposit gold nanoparticles. The CeO2/Bi2Mo1−xRuxO6 and Au/Bi2Mo1−xRuxO6 catalysts were characterized using SEM microscopy and XRD. Furthermore, energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy were used. Tests were carried out for the supported catalysts in CO oxidation, and high conversion values, nearing 100%, was observed in a temperature range of 100 to 250 °C. The results showed that the best system was the Au/Bi2Mo0.95Ru0.05O6 catalyst, with CO oxidation starting at 50 °C and reaching 100% conversion at 186 °C.

scholarly journals Deep oxidative desulfurization of model fuels catalysed by immobilized ionic liquid on MIL-100(Fe)

RSC Advances ◽  
2019 ◽  
Vol 9 (38) ◽  
pp. 21804-21809 ◽  
Author(s):  
WanXin Yang ◽  
Guoqing Guo ◽  
Zhihong Mei ◽  
Yinghao Yu
Keyword(s):  
Ionic Liquid ◽  
High Efficiency ◽  
Oxidative Desulfurization ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
Wet Impregnation Method

ILs@MIL-100 composites were synthesized via the wet impregnation method and applied in deep oxidative desulfurization of gasoline with high efficiency.

CeO2 nanodots decorated ketjen black for high performance lithium–sulfur batteries

RSC Advances ◽  
2016 ◽  
Vol 6 (112) ◽  
pp. 111190-111196 ◽  
Author(s):  
Xinye Qian ◽  
Lina Jin ◽  
Lin Zhu ◽  
Shanshan Yao ◽  
Dewei Rao ◽  
...  
Keyword(s):  
High Performance ◽  
Impregnation Method ◽  
Wet Impregnation ◽  
Lithium Sulfur Battery ◽  
Lithium Sulfur Batteries ◽  
Sulfur Battery ◽  
Wet Impregnation Method ◽  
Lithium Sulfur

A CeO2 nanodots decorated ketjen black composite was fabricated by a simple wet impregnation method and used as the host of sulfur for a lithium–sulfur battery.

scholarly journals Ordered SnO2@C Flake Array as Catalyst Support for Improved Electrocatalytic Activity and Cathode Durability in PEMFCs

Nanomaterials ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2412
Author(s):  
Zhaoyi Yang ◽  
Ming Chen ◽  
Baizeng Fang ◽  
Gaoyang Liu
Keyword(s):  
Electrochemical Impedance ◽  
Proton Exchange ◽  
Pt Catalyst ◽  
Carbon Paper ◽  
Potential Range ◽  
Active Surface Area ◽  
Reduction Peak ◽  
Electrode Structure ◽  
Positive Interaction ◽  
Supported Pt Catalyst

Pt-SnO2@C-ordered flake array was developed on carbon paper (CP) as an integrated cathode for proton exchange membrane fuel cell through a facile hydrothermal method. In the integrated cathode, Pt nanoparticles were deposited uniformly with a small particle size on the SnO2@C/CP support. Electrochemical impedance spectroscopy analysis revealed lower impedance in a potential range of 0.3–0.5 V for the ordered electrode structure. An electrochemically active surface area and oxygen reduction peak potential determined by cyclic voltammetry measurement verified the synergistic effect between Pt and SnO2, which enhanced the electrochemical catalytic activity. Besides, compared with the commercial carbon-supported Pt catalyst, the as-developed SnO2@C/CP-supported Pt catalyst demonstrated better stability, most likely due to the positive interaction between SnO2 and the carbon coating layer.

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