scholarly journals Catalytic and Electrochemical Properties of Ag Infiltrated Perovskite Coatings for Propene Deep Oxidation

Catalysts ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 729
Author(s):  
Thai Giang Truong ◽  
Benjamin Rotonnelli ◽  
Mathilde Rieu ◽  
Jean-Paul Viricelle ◽  
Ioanna Kalaitzidou ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Ag Nanoparticles ◽  
Screen Printing ◽  
Catalytic Properties ◽  
Deep Oxidation ◽  
Electrochemical Performances ◽  
Catalytic Layer ◽  
Propene Oxidation ◽  
Ion Conductor ◽  
Rate Determining Step

This study reports the catalytic properties of Ag nanoparticles dispersed on mixed ionic and electronic conducting layers of LSCF (La0.6Sr0.4Co0.2Fe0.8O3) for propene combustion. A commercial and a synthesized LSCF powder were deposited by screen-printing or spin-coating on dense yttria-stabilized zirconia (YSZ) substrates, an oxygen ion conductor. Equal loadings (50 µg) of Ag nanoparticles were dispersed via drop-casting on the LSCF layers. Electrochemical and catalytic properties have been investigated up to 300 °C with and without Ag in a propene/oxygen feed. The Ag nanoparticles do not influence the electrochemical reduction of oxygen, suggesting that the rate-determining step is the charge transfer at the triple phase boundaries YSZ/LSCF/gas. The anodic electrochemical performances correlate well with the catalytic activity for propene oxidation. This suggests that the diffusion of promoting oxygen ions from YSZ via LSCF grains can take place toward Ag nanoparticles and promote their catalytic activity. The best specific catalytic activity, achieved for a LSCF catalytic layer prepared by screen-printing from the commercial powder, is 800 times higher than that of a pure Ag screen-printed film.

scholarly journals The Study on the Reaction Order and Kinetics of Total Oxidation Reaction of m-xylene over LaMnO3 Perovskite Catalyst

2018 ◽  
Vol 34 (3) ◽  
Author(s):  
Tran Thi Thu Huyen ◽  
Dang Thi Minh Hue ◽  
Nguyen Thi Tuyet Mai ◽  
Tran Thi Luyen ◽  
Nguyen Thi Lan
Keyword(s):  
Catalytic Activity ◽  
Reaction Order ◽  
Catalytic Properties ◽  
Sol Gel ◽  
Deep Oxidation ◽  
Perovskite Oxide ◽  
Mixed Metal Oxide ◽  
Total Oxidation ◽  
Kinetics Of ◽  
Perovskite Type

Gases of m-xylene is one of the popurlar toxic pollutants in the exhaust gases, it is emitted into the environment from factories and engines because the fuel in the engine does not burn completely. The best solution in order to remove this toxic gases of m-xylene to protect the environment is transforming them completely into CO2 and H2O by catalysts. Perovskite of LaMnO3 is one of the catalysts that was synthesized and studied the catalytic properties in total oxidation of m-xylene in our previous report. Obtained results showed that the LaMnO3 perovskite has good catalytic characterizations such as large surface area and the amount of α-oxygen adsorbed on the catalyst is large too. So, it exhibits a good catalytic activity in total oxidation of m-xylene at relatively low reaction temperature. In present work, the reaction order  and kinetics of this reaction are determined. The obtained results demonstrated that the reaction order value with respect to m-xylene is equal to about 1, to oxygene is proximately equal to 0 and the order of reaction is equal to about 1. Based on reaction order data, it was thought that the pathway of m-xylene oxidation by air oxygen  over LaMnO3 may be followed through which the Langmuir - Hinshelwood mechanism. Keywords Catalyst, perovskite, oxidation, m-xylene, kinetics References [1] Penã M.A and Fierro J.L.G (2001), << Chemical Stuctures and Performance of Perovskite Oxide>>, Chem. Rev, 101, pp 1981-2018. [2] Seiyama T., Yamazoe N. and Eguchi K. (1985), <<Characterization and Activity of some Mixed Metal Oxide Catalysts>>, Ind. Eng. Chem. Prod. Res. Dev., 24, pp. 19-27.[3] [3] Van Santen R. A., Neurock M. (2006), Molecular Heterogeneous catalysis, Wiley – VCH, pp.62-244. [4] Petrovics, Terlecki - Baricevic A., Karanovic Lj., Kirilov - Stefanov P. , Zdujic M., Dondur V., Paneva D., Mitov I., Rakic V. (2008), <<LaMO3 (M = Mg, Ti, Fe) perovskite type oxides : Preparation, Characterization and Catalytic Properties in Methane deep Oxidation>>, Appl. Catal. B, Env., 79, pp. 186-198. [5] Spinicci R., Tofanari A., Faticanti M., Pettiti I. and Porta P. (2001), <<Hexane Total Oxidation on LaMO3 (M = Mn, Co, Fe) perovskite-type oxides>>, J. Mole. Catal., 176, pp. 247-252. [6] Trần Thị Thu Huyền, Nguyễn Thị Minh Hiền, Nguyễn Hữu Phú (2006), <<Study on the preparation of perovskite oxides La1-xSrxMnO3 (x = 0; 0,3; 0,5) by sol - gel citrate method and their catalytic activity for m-xylene toltal oxidation>>, Hội nghị xúc tác và hấp phụ toàn quốc lần thứ IV, Tp. Hồ Chí Minh, Tr. 477-482.[7] Trần Thị Thu Huyền, Nguyễn Thị Minh Hiền, Nguyễn Hữu Phú (2009), <<Nghiên cứu động học của phản ứng oxi hóa hoàn toàn m-xylen trên các xúc tác perovskit LaMnO3 và La0,7A0,3MnO3 (A = Sr, Ca, Mg)>>, Tạp chí Hóa học, T.47 (6A), Tr 132-136.[8] Geoffrey C. Bond, Catherine Louis, David T. Thompson (2006), <<Catalysis by Gold>>, Catalytic Science Series-Vol.6.

scholarly journals Synthesis of Bimetallic Gold-Silver (Au-Ag) Nanoparticles for the Catalytic Reduction of 4-Nitrophenol to 4-Aminophenol

Catalysts ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 412 ◽  
Author(s):  
Nurafaliana Berahim ◽  
Wan Basirun ◽  
Bey Leo ◽  
Mohd Johan
Keyword(s):  
Silver Nanoparticles ◽  
Catalytic Activity ◽  
Ag Nanoparticles ◽  
Catalytic Properties ◽  
Catalytic Reduction ◽  
Direct Impact ◽  
Reduction Activity ◽  
Relative Composition ◽  
Catalytic Nanoparticles ◽  
Gold Silver

Bimetallic gold-silver nanoparticles as unique catalysts were prepared using seed colloidal techniques. The catalytic capabilities of the nanoparticles were ascertained in the reduction of 4-nitrophenol to 4-aminophenol in the presence of sodium borohydride. Our results clearly showed that the rate of 4-NP reduction to 4-AP increased with a corresponding decrease in the diameter of the bimetallic NPs. The Au-Ag nanoparticles prepared with 5.0 mL Au seed volume indicated higher reduction activity, which was approximately 1.2 times higher than that of 2.0 mL Au seed volume in the reductive conversion of 4-NP to 4-AP. However, the monometallic NPs showed relatively less catalytic activity in the reductive conversion of 4-NP to 4-AP compared to bimetallic Au-Ag nanoparticles. Our studies also reinforced the improved catalytic properties of the bimetallic Au-Ag nanoparticles structure with a direct impact of the size or diameter and relative composition of the bimetallic catalytic nanoparticles.

Decomposition of hydrogen peroxide on a two-component NiO-CdO catalyst and the effect of ionizing radiation on its catalytic properties

1979 ◽  
Vol 44 (4) ◽  
pp. 1015-1022 ◽  
Author(s):  
Viliam Múčka
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Nickel Oxide ◽  
Catalytic Properties ◽  
Cadmium Oxide ◽  
Chemisorb Oxygen ◽  
Composition Region ◽  
Chemisorbed Oxygen ◽  
Two Component

The catalytic properties of two-component catalyst nickel oxide-cadmium oxide with the proportions of the components covering the whole composition region 0-100% were examined by studying the decomposition of hydrogen peroxide in aqueous solution on it. In the range 0-25 mol.% CdO, cadmium oxide is found to affect infavourably the ability of nickel oxide to chemisorb oxygen. The amount of the chemisorbed oxygen increases several times on gamma irradiation of the samples. The effect of cadmium oxide on the catalytic activity of the system shows up in fresh samples only indirectly via the changed amount of the oxygen chemisorbed. In older samples the initial catalytic activity of the system is changed, which can be explained based on the concept of bivalent catalytic centres in terms of the co-action of the catalytic centres of the two oxides, which are in equilibrium. The irradiation of the system under study speeds up the processes leading to the establishing of this equilibrium which is thermally very stable, and results in a substantial increase of the catalytic activity of the samples investigated.

Hydrogen peroxide decomposition on a two-component CuO-Cr2O3 catalyst

1988 ◽  
Vol 53 (8) ◽  
pp. 1636-1646 ◽  
Author(s):  
Viliam Múčka ◽  
Kamil Lang
Keyword(s):  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Extreme Values ◽  
Catalytic Properties ◽  
Active Components ◽  
Catalytic Systems ◽  
Heterogeneous Catalytic ◽  
Peroxide Decomposition ◽  
Two Component ◽  
Catalytically Active

Some physical and catalytic properties of the two-component copper(II)oxide-chromium(III)oxide catalyst with different content of both components were studied using the decomposition of the aqueous solution of hydrogen peroxide as a testing reaction. It has been found that along to both basic components, the system under study contains also the spinel structure CuCr2O4, chromate washable by water and hexavalent ions of chromium unwashable by water. The soluble chromate is catalytically active. During the first period of the reaction the equilibrium is being established in both homogeneous and heterogeneous catalytic systems. The catalytic activity as well as the specific surface area of the washed solid is a non-monotonous function of its composition. It seems highly probable that the extreme values of both these quantities are not connected with the detected admixtures in the catalytic system. The system under study is very insensitive with regard to the applied doses of gamma radiation. Its catalytic properties are changed rather significantly after the thermal treatment and particularly after the partial reduction to low degree by hydrogen. The observed changes of the catalytic activity of the system under study are very probably in connection with the changes of the valence state of the catalytically active components of the catalyst.

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 Synthesis of Hierarchical MOR-Type Zeolites with Improved Catalytic Properties

Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4508
Author(s):  
Zeinab Mcheik ◽  
Ludovic Pinard ◽  
Joumana Toufaily ◽  
Tayssir Hamieh ◽  
T. Jean Daou
Keyword(s):  
Catalytic Activity ◽  
Amorphous Materials ◽  
Essential Role ◽  
Aluminum Content ◽  
Catalytic Properties ◽  
Hexadecyltrimethylammonium Bromide ◽  
Zeolite Framework ◽  
Ctab Concentration ◽  
Porous Volume ◽  
Synthesis Medium

Hierarchical MOR-type zeolites were synthesized in the presence of hexadecyltrimethylammonium bromide (CTAB) as a porogen agent. XRD proved that the concentration of CTAB in the synthesis medium plays an essential role in forming pure hierarchical MOR-type material. Above a CTAB concentration of 0.04 mol·L−1, amorphous materials are observed. These hierarchical mordenite possess a higher porous volume compared to its counterpart conventional micrometer crystals. Nitrogen sorption showed the presence of mesoporosity for all mordenite samples synthesized in the presence of CTAB. The creation of mesopores due to the presence of CTAB in the synthesis medium does not occur at the expense of zeolite micropores. In addition, mesoporous volume and BET surface seem to increase upon the increase of CTAB concentration in the synthesis medium. The Si/Al ratio of the zeolite framework can be increased from 5.5 to 9.1 by halving the aluminum content present in the synthesis gel. These synthesized hierarchical MOR-type zeolites possess an improved catalytic activity for n-hexane cracking compared to large zeolite crystals obtained in the absence of CTAB.

Designing heterostructurated core@satellites Prussian Blue Analogue@Au-Ag nanoparticles: effect on the magnetic properties and catalytic activity

2021 ◽  
Author(s):  
Ekaterina Mamontova ◽  
María Rodríguez-Castillo ◽  
Erwan Oliviero ◽  
Yannick Guari ◽  
Joulia Larionova ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Catalytic Activity ◽  
Prussian Blue ◽  
Molecular Complex ◽  
Ag Nanoparticles ◽  
Prussian Blue Analogue

We report in this article new magneto-plasmonic core@satellites Prussian Blue Analogue (PBA)@Au-Ag nanoheterostructures obtained by using a post-synthetic impregnation of a bimetallic [AuI2AgI2(C6F5)4(OEt2)2]n molecular complex with the ferromagnetic K+/Ni2+/[Cr(CN)6]3− PBA...

Synthesis of heteroleptic phosphine–copper(i) complexes: fluorescence sensing and catalytic properties

2021 ◽  
Author(s):  
Chen-Lin Luo ◽  
Chu-Xing Hu ◽  
Ping Shang ◽  
Guan-Zhao Wen ◽  
Jia-Jun Zhu ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Catalytic Properties ◽  
Silver Ions ◽  
High Catalytic Activity ◽  
Diphosphine Ligands ◽  
Fluorescence Sensing ◽  
Cuaac Reaction

A series of heteroleptic Cu(i) complexes were precisely synthesized using different bipyridine and diphosphine ligands. These complexes exhibited fluorescence sensing towards silver ions and high catalytic activity towards the CuAAC reaction.

A monovacant heteropolytungstate-incorporated trimeric carbonyl rhenium cluster, [(AsW11O39){Re(CO)3}3(μ3-OH)(μ2-OH)]6−: synthesis, structure and catalytic properties

RSC Advances ◽  
2014 ◽  
Vol 4 (55) ◽  
pp. 28848-28851 ◽  
Author(s):  
Yanhui Zhang ◽  
Dongdi Zhang ◽  
Zhiyuan Huo ◽  
Pengtao Ma ◽  
Jingyang Niu ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
High Selectivity ◽  
Catalytic Properties ◽  
The Novel ◽  
Rhenium Cluster

The novel undecatungstoarsenate-supported carbonyl rhenium derivative exhibits prominent catalytic activity and high selectivity in the cycloaddition of epoxides.

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