scholarly journals A Highly Active Au/In2O3-ZrO2 Catalyst for Selective Hydrogenation of CO2 to Methanol

Catalysts ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1360
Author(s):  
Zhe Lu ◽  
Kaihang Sun ◽  
Jing Wang ◽  
Zhitao Zhang ◽  
Changjun Liu

A novel gold catalyst supported by In2O3-ZrO2 with a solid solution structure shows a methanol selectivity of 70.1% and a methanol space–time yield (STY) of 0.59 gMeOH h−1 gcat−1 for CO2 hydrogenation to methanol at 573 K and 5 MPa. The ZrO2 stabilizes the structure of In2O3, increases oxygen vacancies, and enhances CO2 adsorption, causing the improved activity.

2021 ◽  
Author(s):  
Komal N. Patil ◽  
Divya Prasad ◽  
Jayesh T. Bhanushali ◽  
Bhalchandra Kakade ◽  
Arvind H. Jadhav ◽  
...  

Selective hydrogenation of cinnamaldehyde to hydrocinnamaldehyde is captivating due to its industrial relevance. Herein, two-step synthesis method was adopted to develop oxygen vacancies in Pd@ZrO2 catalysts. The oxygen vacancies were...


1997 ◽  
Vol 496 ◽  
Author(s):  
Masami Kanzaki ◽  
Akihiko Yamaji ◽  
Kazuya Kawakami

ABSTRACTBrownmillerite(Ca2Al2O5-Ca2Fe2O5 solid solution) structure can be regarded as an oxygen-ion deficient perovskite structure. Because of high proportion of the oxygen vacancies in the structure, this material could be a candidate of fast oxide-ion conductor. Goodenough et al. indeed observed a first-order transition to a fast oxide-ion conductor at 930° C for Ba2In2O5 which adapts brownmillerite structure at ambient temperature. Molecular dynamics simulation was employed to study oxygen ion diffusion and phase transition of Ba2In2O5. The structure was well simulated at 300 K. When the system was heated, the original orthogonal cell transformed to a tetragonal cell at 2300 K. Inspection of the structure revealed that oxygen ions started to migrate from their original sites to nearest vacant oxygen sites at this temperature. The diffusion was restricted for the oxygen sites around In-tetrahedron, resulting highly anisotropie diffusion on the ac plane. At 4600 K it further transformed to an oxygen vacancies-disordered cubic perovskite structure. Although predicted transition temperature were apparently overestimated, the transition way to the phases with high oxygen ion diffusivity is consistent with the experimental results from electrical conductivity measurements. The high temperature cubic phase shows large ion conductivity. It is of interest to examine whether or not the cubic phase stabilizes in the low temperature region by making solid solution of another elements. We found that the cubic phase is stabilized below 500° C without any decrease of conductivity in BaIn1.9Ce0.1Oy and Ba2In1.8Nb0.2O5.


Author(s):  
L. E. Afanasieva

The article is devoted to the metallographic analysis of the M2 high-speed steel granules. The study is based on the investigation of the microstructure of the M2 high-speed steel granules obtained by melt atomization. It is demonstrated that granules of similar size can harden both by chemically separating and chemically non-separating mechanism. These last ones have supersaturated solid solution structure of the liquid melt composition, a dispersed dendritic-cellular structure and an increased microhardness HV = 10267±201 MPa.


Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 452
Author(s):  
Michalis Konsolakis ◽  
Maria Lykaki

The rational design and fabrication of highly-active and cost-efficient catalytic materials constitutes the main research pillar in catalysis field. In this context, the fine-tuning of size and shape at the nanometer scale can exert an intense impact not only on the inherent reactivity of catalyst’s counterparts but also on their interfacial interactions; it can also opening up new horizons for the development of highly active and robust materials. The present critical review, focusing mainly on our recent advances on the topic, aims to highlight the pivotal role of shape engineering in catalysis, exemplified by noble metal-free, CeO2-based transition metal catalysts (TMs/CeO2). The underlying mechanism of facet-dependent reactivity is initially discussed. The main implications of ceria nanoparticles’ shape engineering (rods, cubes, and polyhedra) in catalysis are next discussed, on the ground of some of the most pertinent heterogeneous reactions, such as CO2 hydrogenation, CO oxidation, and N2O decomposition. It is clearly revealed that shape functionalization can remarkably affect the intrinsic features and in turn the reactivity of ceria nanoparticles. More importantly, by combining ceria nanoparticles (CeO2 NPs) of specific architecture with various transition metals (e.g., Cu, Fe, Co, and Ni) remarkably active multifunctional composites can be obtained due mainly to the synergistic metalceria interactions. From the practical point of view, novel catalyst formulations with similar or even superior reactivity to that of noble metals can be obtained by co-adjusting the shape and composition of mixed oxides, such as Cu/ceria nanorods for CO oxidation and Ni/ceria nanorods for CO2 hydrogenation. The conclusions derived could provide the design principles of earth-abundant metal oxide catalysts for various real-life environmental and energy applications.


2021 ◽  
Vol 14 (2) ◽  
pp. 102951
Author(s):  
Nagaraju Pasupulety ◽  
Abdurahim A. Al-Zahrani ◽  
Muhammad A. Daous ◽  
Seetharamulu Podila ◽  
Hafedh Driss

Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 772
Author(s):  
Yanxiong Liu ◽  
Changhua Hu ◽  
Longchun Bian

The correlation between the occurrence state of surface Pd species of Pd/CeO2 for lean CH4 combustion is investigated. Herein, by using a reduction-deposition method, we have synthesized a highly active 0.5% PdO/CeO2-RE catalyst, in which the Pd nanoparticles are evenly dispersed on the CeO2 nanorods CeO2-R. Based on comprehensive characterization, we have revealed that the uniformly dispersed Pd nanoparticles with a particle size distribution of 2.3 ± 0.6 nm are responsible for the generation of PdO and PdxCe1−xO2−δ phase with –Pd2+–O2−–Ce4+– linkage, which can easily provide oxygen vacancies and facilitate the transfer of reactive oxygen species between the CeO2-R and Pd species. As a consequence, the remarkable catalytic activity of 0.5% Pd/CeO2-RE is related to the high concentration of PdO species on the surface of the catalyst and the synergistic interaction between the Pd species and the CeO2 nanorod.


Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1058 ◽  
Author(s):  
Leone Frusteri ◽  
Catia Cannilla ◽  
Serena Todaro ◽  
Francesco Frusteri ◽  
Giuseppe Bonura

Ternary CuxZnyAlz catalysts were prepared using the hydrotalcite (HT) method. The influence of the atomic x:y:z ratio on the physico-chemical and catalytic properties under CO2 hydrogenation conditions was probed. The characterization data of the investigated catalysts were obtained by XRF, XRD, BET, TPR, CO2-TPD, N2O chemisorption, SEM, and TEM techniques. In the “dried” catalyst, the typical structure of a hydrotalcite phase was observed. Although the calcination and subsequent reduction treatments determined a clear loss of the hydrotalcite structure, the pristine phase addressed the achievement of peculiar physico-chemical properties, also affecting the catalytic activity. Textural and surface effects induced by the zinc concentration conferred a very interesting catalyst performance, with a methanol space time yield (STY) higher than that of commercial systems operated under the same experimental conditions. The peculiar behavior of the hydrotalcite-like samples was related to a high dispersion of the active phase, with metallic copper sites homogeneously distributed among the oxide species, thereby ensuring a suitable activation of H2 and CO2 reactants for a superior methanol production.


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