scholarly journals Heterogeneous Catalytic Synthesis of 2-Methylbenzimidazole from 2-Nitroaniline and Ethanol Over Mg Modified Cu-Pd/γ-Al2O3

Catalysts ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 8 ◽  
Author(s):  
Feng Feng ◽  
Yaqin Deng ◽  
Zheng Cheng ◽  
Xiaoliang Xu ◽  
Qunfeng Zhang ◽  
...  
Keyword(s):  
Active Sites ◽  
Hydrogen Transfer ◽  
High Efficiency ◽  
Simple Procedure ◽  
Direct Synthesis ◽  
Reaction System ◽  
Simple Method ◽  
Heterogeneous Catalytic ◽  
Coupled Reaction ◽  
Al2o3 Catalyst

The direct synthesis of benzimidazoles from 2-nitroaniline and ethanol over Cu-Pd/γ-Al2O3 catalysts has the advantages of requiring easily available starting materials, having high efficiency, and a simple procedure. The modification by Mg of the Cu-Pd/γ-Al2O3 catalyst could improve the catalytic activity significantly. The addition of Mg to the Cu-Pd/γ-Al2O3 catalyst could maintain and promote the formation of CuPd alloy active sites. Meanwhile, the basicity of the support was enhanced appropriately by Mg, which generated more basic sites (Al-Oδ−) to accelerate the dehydrogenation of alcohol and increased the rate of the whole coupled reaction. The 2-nitroaniline was completely converted over Cu-Pd/(Mg)γ-Al2O3 after reacting for six hours, and the yield of 2-methylbenzimidazole was 98.8%. The results of this work provide a simple method to develop a more efficient catalyst for the “alcohol-dehydrogenation, hydrogen transfer and hydrogenation” coupled reaction system.

CONTROLLED FABRICATION OF Nb2O5 HOLLOW NANOSPHERES AND NANOTUBES

2009 ◽  
Vol 23 (31n32) ◽  
pp. 3769-3775 ◽  
Author(s):  
FEI LIU ◽  
DONGFENG XUE
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Simple Procedure ◽  
Hollow Spheres ◽  
Reaction System ◽  
Inorganic Materials ◽  
Molar Ratio ◽  
Hollow Nanospheres ◽  
Simple Method ◽  
Wide Range

A simple procedure for one-step growing Nb 2 O 5 hollow nanospheres and nanotubes was proposed. The final products were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and transmission electron microscopy (TEM). The as-obtained hollow spheres present a polycrystal surface while the nanotubes possess single crystal walls. Moreover, the factors that could impact the product morphology and crystal structure were discussed, and the corresponding mechanism was proposed accordingly. The crystal structure and morphology of products can be easily tuned by adjusting the molar ratio of Nb / Ti used, which determines the amount of F - ions existing in the reaction system. The as-obtained Nb 2 O 5 hollow nanospheres and nanotubes may exhibit enhanced applications in a wide range of areas. Additionally, it is rational to expect that this simple method can be extended to systems of other inorganic materials with desired morphologies.

Catalytic Neutralization of Naphthenic Acid from Petroleum Crude Oil by Using Cerium Oxide Catalyst and 2- Methylimidazole in Polyethylene Glycol

2020 ◽  
Vol 13 ◽  
Author(s):  
Norshahidatul Akmar Mohd Shohaimi ◽  
Norfakhriah Jelani ◽  
Ahmad Zamani Ab Halim ◽  
Nor Hakimin Abdullah ◽  
Nurasmat Mohd Shukri
Keyword(s):  
Polyethylene Glycol ◽  
Crude Oil ◽  
Cerium Oxide ◽  
Active Sites ◽  
Naphthenic Acid ◽  
Naphthenic Acids ◽  
Catalyst Loading ◽  
High Concentration ◽  
Oil Refineries ◽  
Al2o3 Catalyst

: The presence of relatively high naphthenic acid in crude oil may contribute to the major corrosion in oil pipelines and distillation units in crude oil refineries. Thus, high concentration Naphthenic Acids crude oil is considered tobe of low quality and is marketed at lower prices. In order to overcome this problem, neutralization method had been developed to reduce the TAN value in crude oil. In this study, crude oil from Petronas Penapisan Melaka was investigated. The parameters studied were reagent concentration, catalyst loading, calcination temperature and reusability of the potential catalyst. Basic chemical used were 2- methylimidazole in polyethylene glycol (PEG 600) with concentration 100, 500 and 1000 ppm. Cerium oxide-based catalysts supported onto alumina prepared with different calcination temperatures. The catalyst was characterized by using Brunauer-Emmett-Teller (BET), Fourier Transform Infrared Spectroscopy (FTIR) and Thermogravimetry Analysis-Differential Thermal Gravity (TGA-DTG) to study physical properties of the catalyst. The Ce/Al2O3 catalyst calcined at 1000°C was the best catalyst due to larger surface area formation which lead to increment of active sites thus will boost the catalytic activity. The result showed that the Ce/Al2O3 catalyst meet Petronas requirement as the TAN value reduced to 0.6 mgKOH/g from original TAN value of 4.22 mgKOH/g. The best reduction of TAN was achieved by using catalyst loading of 0.39% and reagent of 1000 ppm.

Kinetics of the catalytic hydrodesulphurization reaction system; hydrogenolysis of thiophene

1980 ◽  
Vol 45 (10) ◽  
pp. 2728-2741 ◽  
Author(s):  
Pavel Fott ◽  
Petr Schneider
Keyword(s):  
Atmospheric Pressure ◽  
Active Sites ◽  
Flow Reactor ◽  
Kinetic Equations ◽  
Reaction System ◽  
Reaction Products ◽  
Molybdenum Catalyst ◽  
Cobalt Molybdenum Catalyst ◽  
Kinetics Of ◽  
Reaction Schemes

Kinetics have been studied of the reaction system taking place during the reaction of thiophene on the cobalt-molybdenum catalyst in a gradientless circulation flow reactor at 360 °C and atmospheric pressure. Butane has been found present in a small amount in the reaction products even at very low conversion. In view of this, consecutive and parallel-consecutive (triangular) reaction schemes have been proposed. In the former scheme the appearance of butane is accounted for by rate of desorption of butene being comparable with the rate of its hydrogenation. According to the latter scheme part of the butane originates from thiophene via a different route than through hydrogenation of butene. Analysis of the kinetic data has revealed that the reaction of thiophene should be considered to take place on other active sites than that of butene. Kinetic equations derived on this assumption for the consecutive and the triangular reaction schemes correlate experimental data with acceptable accuracy.

scholarly journals Enhanced catalytic ozonation of ibuprofen using a 3D structured catalyst with MnO2 nanosheets on carbon microfibers

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Guhankumar Ponnusamy ◽  
Hajar Farzaneh ◽  
Yongfeng Tong ◽  
Jenny Lawler ◽  
Zhaoyang Liu ◽  
...  
Keyword(s):  
Removal Efficiency ◽  
Active Sites ◽  
Low Cost ◽  
Three Dimensional ◽  
Industrial Applications ◽  
Catalytic Ozonation ◽  
Heterogeneous Catalytic ◽  
Structured Catalyst ◽  
Dimensional Network ◽  
Carbon Microfibers

AbstractHeterogeneous catalytic ozonation is an effective approach to degrade refractory organic pollutants in water. However, ozonation catalysts with combined merits of high activity, good reusability and low cost for practical industrial applications are still rare. This study aims to develop an efficient, stable and economic ozonation catalyst for the degradation of Ibuprofen, a pharmaceutical compound frequently detected as a refractory pollutant in treated wastewaters. The novel three-dimensional network-structured catalyst, comprising of δ-MnO2 nanosheets grown on woven carbon microfibers (MnO2 nanosheets/carbon microfiber), was synthesized via a facile hydrothermal approach. Catalytic ozonation performance of Ibuprofen removal in water using the new catalyst proves a significant enhancement, where Ibuprofen removal efficiency of close to 90% was achieved with a catalyst loading of 1% (w/v). In contrast, conventional ozonation was only able to achieve 65% removal efficiency under the same operating condition. The enhanced performance with the new catalyst could be attributed to its significantly increased available surface active sites and improved mass transfer of reaction media, as a result of the special surface and structure properties of this new three-dimensional network-structured catalyst. Moreover, the new catalyst displays excellent stability and reusability for ibuprofen degradation over successive reaction cycles. The facile synthesis method and low-cost materials render the new catalyst high potential for industrial scaling up. With the combined advantages of high efficiency, high stability, and low cost, this study sheds new light for industrial applications of ozonation catalysts.

scholarly journals Adsorption and Photocatalytic Reduction of Carbon Dioxide on TiO2

Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 47
Author(s):  
Oleksandr Shtyka ◽  
Viktar Shatsila ◽  
Radoslaw Ciesielski ◽  
Adam Kedziora ◽  
Waldemar Maniukiewicz ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Active Sites ◽  
High Efficiency ◽  
Chemical Potential ◽  
Band Gap Energy ◽  
Electromagnetic Spectrum ◽  
Reaction Intermediates ◽  
Factors Affecting ◽  
Phase Reduction ◽  
Reduction Of Co2

The photocatalytic activity of TiO2 depends on numerous factors, such as the chemical potential of electrons, charge transport properties, band-gap energy, and concentration of surface-active sites. A lot of research has been dedicated to determining the properties that have the most significant influence on the photocatalytic activity of semiconductors. Here, we demonstrated that the activity of TiO2 in the gas-phase reduction of CO2 is governed mainly by the desorption rate of the reaction intermediates and final products. This indicates that the specific surface area of TiO2 and binding strength of reaction intermediates and products are the main factors affecting the photocatalytic activity of TiO2 in the investigated process. Additionally, it was shown that rutile exhibits higher photocatalytic activity than anatase/rutile mixtures mainly due to its high efficiency in the visible portion of the electromagnetic spectrum.

Promoter role of tungsten in W-Pd/Al2O3 catalyst for direct synthesis of H2O2: Modification of Pd/PdO ratio

2021 ◽  
pp. 118392
Author(s):  
Meijia Zhang ◽  
Yibin Luo ◽  
Dengfeng Wu ◽  
Qian Li ◽  
Haoxiang Xu ◽  
...  
Keyword(s):  
Direct Synthesis ◽  
Al2o3 Catalyst

Microwave Activation of Homogeneous and Heterogeneous Catalytic Reactions

1997 ◽  
Vol 62 (2) ◽  
pp. 347-354 ◽  
Author(s):  
Milan Hájek
Keyword(s):  
Active Sites ◽  
Specific Effect ◽  
Point Of View ◽  
Heterogeneous Reactions ◽  
Microwave Activation ◽  
Rate Enhancement ◽  
Heterogeneous Catalytic ◽  
Order Of Magnitude ◽  
And Performance ◽  
Alkylation Reactions

Microwave heating was applied in homogeneous and in heterogeneous reactions and the results were compared from the point of view of activation of chemical reactions. Reactions including the addition of halo compounds to alkenes catalyzed by copper and ruthenium complexes in different solvents and NaY zeolite catalyzed alkylation of secondary amine in the absence of solvent were studied as model reactions to compare possibilities of microwave activation of reactants and catalysts. Rate enhancement of over one order of magnitude in homogeneous reactions was caused mainly by thermal dielectric heating effect which resulted from the effective coupling of microwaves to polar solvents. Activation of reactants and catalysts was very low if any. In heterogeneously catalyzed alkylation reactions highly efficient activation of zeolite catalyst was recorded. The results indicated that the best reaction conditions were in experiments when both activation of catalyst and performance of reaction were carried out under microwave conditions. Rate enhancement was most probably caused by "hot spots" or by "selective heating" of active sites. In both homogeneous and heterogeneous reactions non-thermal activation (specific effect) was excluded.

scholarly journals Thermodynamics and Kinetic Modeling of the ZnSO4.H2O Thermal Decomposition in the Presence of a Pd/Al2O3 Catalyst

Energies ◽  
2022 ◽  
Vol 15 (2) ◽  
pp. 548
Author(s):  
Gabriela V. T. Kurban ◽  
Artur S. C. Rego ◽  
Nathalli M. Mello ◽  
Eduardo A. Brocchi ◽  
Rogério C. S. Navarro ◽  
...  
Keyword(s):  
Activation Energy ◽  
Thermal Decomposition ◽  
Zinc Sulfate ◽  
Thermodynamic Assessment ◽  
Reaction System ◽  
Decomposition Temperature ◽  
Kinetic Behavior ◽  
Proposed Model ◽  
Al2o3 Catalyst ◽  
Iodine Reaction

The sulfur–iodine thermochemical water-splitting cycle is a promising route proposed for hydrogen production. The decomposition temperature remains a challenge in the process. Catalysts, such as Pd supported on Al2O3, are being considered to decrease reaction temperatures. However, little is known regarding the kinetic behavior of such systems. In this work, zinc sulfate thermal decomposition was studied through non-isothermal thermogravimetric analysis to understand the effect of a catalyst within the sulfur–iodine reaction system context. The findings of this analysis were also related to a thermodynamic assessment. It was observed that the presence of Pd/Al2O3 modified the reaction mechanism, possibly with some intermediate reactions that were suppressed or remarkably accelerated. The proposed model suggests that zinc sulfate transformation occurred in two sequential stages without the Pd-based material. Activation energy values of 238 and 368 kJ.mol−1 were calculated. In the presence of Pd/Al2O3, an activation energy value of 204 kJ.mol−1 was calculated, which is lower than observed previously.

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