Effect of Bimetallic Doping in Cobalt Titanate for Methane Reforming

2019 ◽  
Author(s):  
Disha Jain
Keyword(s):  
Catalytic Activity ◽  
Low Cost ◽  
Coke Deposition ◽  
Ex Situ ◽  
Pt Catalyst ◽  
High Catalytic Activity ◽  
Methane Reforming ◽  
Metal Support Interaction ◽  
Metal Support ◽  
Surface Intermediates

<p>Supported Ni catalysts are extensively studied for methane reforming due to their high catalytic activity and low cost. However, these catalysts undergo deactivation due to coke deposition and oxidation of Ni particles. In the present work, Ni and Pt substituted CoTiO<sub>3</sub> were synthesized and studied for steam (SRM) and dry (DRM) reforming of methane. The catalytic activity of monometallic and bimetallic Ni-Pt catalyst was compared for SRM and reducibility studies were done to highlight the change in metal-support interaction in the synthesized samples. Ex situ and in situ characterization were performed to understand the change in catalyst surface and the nature of surface intermediates formed during the reaction. Consequently, surface reaction mechanism was proposed and kinetic parameters were determined by fitting experimental data.</p><br>

Effect of Bimetallic Doping in Cobalt Titanate for Methane Reforming

2019 ◽  
Author(s):  
Disha Jain
Keyword(s):  
Catalytic Activity ◽  
Low Cost ◽  
Coke Deposition ◽  
Ex Situ ◽  
Pt Catalyst ◽  
High Catalytic Activity ◽  
Methane Reforming ◽  
Metal Support Interaction ◽  
Metal Support ◽  
Surface Intermediates

<p>Supported Ni catalysts are extensively studied for methane reforming due to their high catalytic activity and low cost. However, these catalysts undergo deactivation due to coke deposition and oxidation of Ni particles. In the present work, Ni and Pt substituted CoTiO<sub>3</sub> were synthesized and studied for steam (SRM) and dry (DRM) reforming of methane. The catalytic activity of monometallic and bimetallic Ni-Pt catalyst was compared for SRM and reducibility studies were done to highlight the change in metal-support interaction in the synthesized samples. Ex situ and in situ characterization were performed to understand the change in catalyst surface and the nature of surface intermediates formed during the reaction. Consequently, surface reaction mechanism was proposed and kinetic parameters were determined by fitting experimental data.</p><br>

scholarly journals The effect of interfacial engineering on the deactivation resistance of nickel-based catalysts for dry reforming of methane

2021 ◽  
Vol 2076 (1) ◽  
pp. 012041
Author(s):  
Jinmiao Zhang ◽  
Mudi Zheng ◽  
Yuqing Zhou ◽  
Xingyuan Gao
Keyword(s):  
Catalytic Activity ◽  
Low Cost ◽  
Chemical Properties ◽  
Dry Reforming ◽  
Sulfur Poisoning ◽  
Dry Reforming Of Methane ◽  
Interfacial Engineering ◽  
Metal Support Interaction ◽  
Metal Metal ◽  
Metal Support

Abstract Methane dry reforming reaction (DRM) can convert CO2 and CH4, two kinds of greenhouse gases with very stable chemical properties, to produce syngas, which can be used to synthesize valuable industrial products. Nickel-based catalysts have been widely used in DRM because of their low cost and good catalytic activity. However, nickel application is limited by such as high-temperature metal sintering, carbon deposition and catalyst poisoning, which restricts the industrial application in DRM reaction. Compared with single metal nickel, the selective doping of multi metals and supports shows higher catalytic activity and anti poisoning tolerance due to changing the chemical and structural properties of the catalyst by enhancing the alloy effect and the force between metal and support. This paper mainly reviews the catalysts with anti-coking, anti-sintering and anti-sulfur poisoning by tuning the metal-metal interaction and metal-support interaction (MSI) in DRM. The modification strategies in interfacial engineering and structure-performance relationship are discussed, and the existing difficulties and future development of Ni-based catalysts are proposed.

Strong metal-support interaction between Pt and SiO2 following high-temperature reduction: a catalytic interface for propane dehydrogenation

2017 ◽  
Vol 53 (51) ◽  
pp. 6937-6940 ◽  
Author(s):  
Lidan Deng ◽  
Hiroki Miura ◽  
Tetsuya Shishido ◽  
Saburo Hosokawa ◽  
Kentaro Teramura ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
High Temperature ◽  
Pt Nanoparticles ◽  
Propane Dehydrogenation ◽  
High Catalytic Activity ◽  
Support Interaction ◽  
Temperature Reduction ◽  
Metal Support Interaction ◽  
Metal Support ◽  
Smsi Effect

Pt/SiO2 directly reduced in H2 at 1073 K exhibited a high catalytic activity in propane dehydrogenation, primarily attributed to the electronic modification of Pt nanoparticles by the SMSI effect.

Effects of rare earth metal doping on Au/ReZrO2 catalysts for efficient hydrogen generation from formic acid

2021 ◽  
Vol 45 (12) ◽  
pp. 5704-5711
Author(s):  
Luming Wu ◽  
Yu Hao ◽  
Shaohua Chen ◽  
Rui Chen ◽  
Pingchuan Sun ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Rare Earth ◽  
Rare Earth Metal ◽  
Oxygen Vacancies ◽  
Hydrogen Generation ◽  
Earth Metal ◽  
Support Interaction ◽  
Metal Support Interaction ◽  
Metal Support ◽  
Metal Doped

Rare earth metal doped ZrO2 can promote the formation of oxygen vacancies in zirconia, which enhances the metal–support interaction, finally promoting catalytic activity of FA dehydrogenation.

scholarly journals High catalytic activity for formaldehyde oxidation of an interconnected network structure composed of δ-MnO2 nanosheets and γ-MnOOH nanowires

2020 ◽  
Vol 8 (4) ◽  
pp. 429-439
Author(s):  
Ying Tao ◽  
Rong Li ◽  
Ai-Bin Huang ◽  
Yi-Ning Ma ◽  
Shi-Dong Ji ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Network Structure ◽  
Manganese Oxides ◽  
Active Oxygen Species ◽  
Low Cost ◽  
High Dispersion ◽  
Hydroxyl Groups ◽  
High Catalytic Activity ◽  
Interconnected Network ◽  
Surface Hydroxyl

AbstractAmong the transition metal oxide catalysts, manganese oxides have great potential for formaldehyde (HCHO) oxidation at ambient temperature because of their high activity, nontoxicity, low cost, and polybasic morphologies. In this work, a MnO2-based catalyst (M-MnO2) with an interconnected network structure was successfully synthesized by a one-step hydrothermal method. The M-MnO2 catalyst was composed of the main catalytic agent, δ-MnO2 nanosheets, dispersed in a nonactive framework material of γ-MnOOH nanowires. The catalytic activity of M-MnO2 for HCHO oxidation at room temperature was much higher than that of the pure δ-MnO2 nanosheets. This is attributed to the special interconnected network structure. The special interconnected network structure has high dispersion and specific surface area, which can provide more surface active oxygen species and higher surface hydroxyl groups to realize rapid decomposition of HCHO.

Trimetallic RuxMoNi Catalysts Supported on SBA-15 for the Hydrodesulfurization of Dibenzothiophene

2018 ◽  
Vol 17 (5) ◽  
Author(s):  
N.L. Torres-García ◽  
R. Huirache-Acuña ◽  
T.A. Zepeda-Partida ◽  
B. Pawelec ◽  
J.L.G. Fierro ◽  
...  
Keyword(s):  
Raman Spectroscopy ◽  
Catalytic Activity ◽  
Chelating Agent ◽  
Active Phase ◽  
Atomic Ratio ◽  
Support Interaction ◽  
Micro Raman Spectroscopy ◽  
Metal Support Interaction ◽  
Sulfided Catalysts ◽  
Metal Support

Abstract In this work, novel trimetallic catalysts based on transition metal sulphides (Ru, Mo and Ni) supported on SBA-15 were synthesized. Citric acid (CA) was used as chelating agent in order to enhance the dispersion of the active phase and minimize the metal-support interaction. Sulfided catalysts were evaluated in the reaction of hydrodesulfurization (HDS) of dibenzothiophene (DBT) at 320 °C and 54.5 atm of total H2 pressure. The effects of different Ru/(Ni + Mo) atomic ratios on the active phase were studied. The catalysts were characterized using Micro-Raman spectroscopy, DRIFTS, XRD, XPS, HR-TEM and SEM techniques. Results have shown that there was a better dispersion of the metallic phases, which improves the physicochemical properties of the catalysts, increasing the catalytic activity. The trimetallic RuxMoNi catalyst with the lowest atomic ratio, have shown superior catalytic activity compared to their higher atomic ratio counterparts. The interaction of the chelating agent improved the catalytic activity, which was superior to that observed for NiMo based catalysts, considered one of the most active hydrotreating catalysts.

Molten salts-assisted synthesis of special open-cell Fe, N co-doped porous carbon as an efficient electrocatalyst for zinc-air batteries

2021 ◽  
Author(s):  
Xiaoying Gao ◽  
Xuan Xie ◽  
Kanjun Sun ◽  
Xiaofei Lei ◽  
Tianyu Hou ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Porous Carbon ◽  
Molten Salts ◽  
Low Cost ◽  
High Catalytic Activity ◽  
Open Cell ◽  
Co Doped ◽  
Excellent Stability ◽  
Zinc Air Batteries

Fe, N co-doped carbon electrocatalyst is one of the most attractive alternatives to Pt/C catalysts due to its high catalytic activity, excellent stability and low cost. However, obtaining stable and...

scholarly journals Improving the Performance of Zn-Air Batteries with N-Doped Electroexfoliated Graphene

Materials ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2115 ◽  
Author(s):  
Anna Ilnicka ◽  
Malgorzata Skorupska ◽  
Piotr Romanowski ◽  
Piotr Kamedulski ◽  
Jerzy P. Lukaszewicz
Keyword(s):  
Catalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Noble Metals ◽  
Electrode Materials ◽  
Low Cost ◽  
Rapid Development ◽  
Reduction Reaction ◽  
Graphene Sheets ◽  
High Catalytic Activity ◽  
Energy Storage Devices

The constantly growing demand for active, durable, and low-cost electrocatalysts usable in energy storage devices, such as supercapacitors or electrodes in metal-air batteries, has triggered the rapid development of heteroatom-doped carbon materials, which would, among other things, exhibit high catalytic activity in the oxygen reduction reaction (ORR). In this article, a method of synthesizing nitrogen-doped graphene is proposed. Few-layered graphene sheets (FL-graphene) were prepared by electrochemical exfoliation of commercial graphite in a Na2SO4 electrolyte with added calcium carbonate as a separator of newly-exfoliated FL-graphene sheets. Exfoliated FL-graphene was impregnated with a suspension of green algae used as a nitrogen carrier. Impregnated FL-graphene was carbonized at a high temperature under the flow of nitrogen. The N-doped FL-graphene was characterized through instrumental methods: high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, and Raman spectroscopy. Electrochemical performance was determined using cyclic voltamperometry and linear sweep voltamperometry to check catalytic activity in ORR. The N-doped electroexfoliated FL-graphene obeyed the four-electron transfer pathways, leading us to further test these materials as electrode components in rechargeable zinc-air batteries. The obtained results for Zn-air batteries are very important for future development of industry, because the proposed graphene electrode materials do not contain any heavy and noble metals in their composition.

scholarly journals Effect of Mg Contents on Catalytic Activity and Coke Formation of Mesoporous Ni/Mg-Aluminate Spinel Catalyst for Steam Methane Reforming

Catalysts ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 828 ◽  
Author(s):  
Hyunjoung Kim ◽  
Young-Hee Lee ◽  
Hongjin Lee ◽  
Jeong-Cheol Seo ◽  
Kyubock Lee
Keyword(s):  
Catalytic Activity ◽  
Coke Formation ◽  
Coke Deposition ◽  
Methane Reforming ◽  
Reaction Conditions ◽  
Ni Catalysts ◽  
Steam Methane Reforming ◽  
Steam Methane ◽  
Spinel Catalysts ◽  
Mg Content

Ni catalysts are most suitable for a steam methane reforming (SMR) reaction considering the activity and the cost, although coke formation remains the main problem. Here, Ni-based spinel catalysts with various Mg contents were developed through the synthesis of mesoporous Mg-aluminate supports by evaporation-induced self-assembly followed by Ni loading via incipient wetness impregnation. The mesoporous Ni/Mg-aluminate spinel catalysts showed high coke resistance under accelerated reaction conditions (0.0014 gcoke/gcat·h for Ni/Mg30, 0.0050 gcoke/gcat·h for a commercial catalyst). The coke resistance of the developed catalyst showed a clear trend: the higher the Mg content, the lower the coke deposition. The Ni catalysts with the lower Mg content showed a higher surface area and smaller Ni particle size, which originated from the difference of the sintering resistance and the exsolution of Ni particles. Despite these advantageous attributes of Ni catalysts, the coke resistance was higher for the catalysts with the higher Mg content while the catalytic activity was dependent on the reaction conditions. This reveals that the enhanced basicity of the catalyst could be the major parameter for the reduction of coke deposition in the SMR reaction.

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