Enhanced low-temperature activity of CO2 methanation over highly-dispersed Ni/TiO2 catalyst

2013 ◽  
Vol 3 (10) ◽  
pp. 2627 ◽  
Author(s):  
Jie Liu ◽  
Changming Li ◽  
Fei Wang ◽  
Shan He ◽  
Hao Chen ◽  
...  
Fuel ◽  
2020 ◽  
Vol 278 ◽  
pp. 118333 ◽  
Author(s):  
Chufei Lv ◽  
Leilei Xu ◽  
Mindong Chen ◽  
Yan Cui ◽  
Xueying Wen ◽  
...  

2015 ◽  
Vol 51 (9) ◽  
pp. 1728-1731 ◽  
Author(s):  
Wenlong Zhen ◽  
Bo Li ◽  
Gongxuan Lu ◽  
Jiantai Ma

A novel high active catalyst Ni@MOF-5 showed unexpected higher activity under the low temperature for CO2 methanation. The characterization results indicated that Ni was in highly dispersed uniform state over MOF-5. This catalyst performed high stability and showed almost no deactivation in long term stability tests up to 100 h.


Author(s):  
Zhiying Zhao ◽  
Qiaorong Jiang ◽  
Qiuxiang Wang ◽  
Mingzhi Wang ◽  
Jiachang Zuo ◽  
...  

2021 ◽  
Author(s):  
lilei zhang ◽  
Botan Li ◽  
Chunyan Liu ◽  
He Tian ◽  
Manzhou Hong ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 618
Author(s):  
Huan Du ◽  
Zhitao Han ◽  
Xitian Wu ◽  
Chenglong Li ◽  
Yu Gao ◽  
...  

Er-modified FeMn/TiO2 catalysts were prepared through the wet impregnation method, and their NH3-SCR activities were tested. The results showed that Er modification could obviously promote SO2 resistance of FeMn/TiO2 catalysts at a low temperature. The promoting effect and mechanism were explored in detail using various techniques, such as BET, XRD, H2-TPR, XPS, TG, and in-situ DRIFTS. The characterization results indicated that Er modification on FeMn/TiO2 catalysts could increase the Mn4+ concentration and surface chemisorbed labile oxygen ratio, which was favorable for NO oxidation to NO2, further accelerating low-temperature SCR activity through the “fast SCR” reaction. As fast SCR reaction could accelerate the consumption of adsorbed NH3 species, it would benefit to restrain the competitive adsorption of SO2 and limit the reaction between adsorbed SO2 and NH3 species. XPS results indicated that ammonium sulfates and Mn sulfates formed were found on Er-modified FeMn/TiO2 catalyst surface seemed much less than those on FeMn/TiO2 catalyst surface, suggested that Er modification was helpful for reducing the generation or deposition of sulfate salts on the catalyst surface. According to in-situ DRIFTS the results of, the presence of SO2 in feeding gas imposed a stronger impact on the NO adsorption than NH3 adsorption on Lewis acid sites of Er-modified FeMn/TiO2 catalysts, gradually making NH3-SCR reaction to proceed in E–R mechanism rather than L–H mechanism. DRIFTS.


Author(s):  
Gabriella Garbarino ◽  
Paweł Kowalik ◽  
Paola Riani ◽  
Katarzyna Antoniak-Jurak ◽  
Piotr Pieta ◽  
...  

Nanomaterials ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 28
Author(s):  
Anastasios I. Tsiotsias ◽  
Nikolaos D. Charisiou ◽  
Ioannis V. Yentekakis ◽  
Maria A. Goula

CO2 methanation has recently emerged as a process that targets the reduction in anthropogenic CO2 emissions, via the conversion of CO2 captured from point and mobile sources, as well as H2 produced from renewables into CH4. Ni, among the early transition metals, as well as Ru and Rh, among the noble metals, have been known to be among the most active methanation catalysts, with Ni being favoured due to its low cost and high natural abundance. However, insufficient low-temperature activity, low dispersion and reducibility, as well as nanoparticle sintering are some of the main drawbacks when using Ni-based catalysts. Such problems can be partly overcome via the introduction of a second transition metal (e.g., Fe, Co) or a noble metal (e.g., Ru, Rh, Pt, Pd and Re) in Ni-based catalysts. Through Ni-M alloy formation, or the intricate synergy between two adjacent metallic phases, new high-performing and low-cost methanation catalysts can be obtained. This review summarizes and critically discusses recent progress made in the field of bimetallic Ni-M (M = Fe, Co, Cu, Ru, Rh, Pt, Pd, Re)-based catalyst development for the CO2 methanation reaction.


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