Hydrogen storage of a novel combined system of LiNH2–NaMgH3: synergistic effects of in situ formed alkali and alkaline-earth metal hydrides

2013 ◽  
Vol 42 (5) ◽  
pp. 1810-1819 ◽  
Author(s):  
Yongtao Li ◽  
Fang Fang ◽  
Yun Song ◽  
Yuesheng Li ◽  
Dalin Sun ◽  
...  
2015 ◽  
Vol 119 (2) ◽  
pp. 934-943 ◽  
Author(s):  
C. Pistidda ◽  
A. Santoru ◽  
S. Garroni ◽  
N. Bergemann ◽  
A. Rzeszutek ◽  
...  

Synlett ◽  
2021 ◽  
Author(s):  
Dongxu Yang ◽  
Linqing Wang

AbstractMagnesium (Mg) is a cheap, non-toxic, and recyclable alkaline earth metal that constitutes about 2% weight in the Earth’s crust. The use of magnesium catalysts to forge chiral moieties in molecules is highly attractive. Based on our work in recent years, we describe the current progress in the development of in situ generated magnesium catalysts and their application in asymmetric synthesis. In this perspective, a critically concise classification of in situ generated magnesium catalytic modes, with relevant examples, is presented, and representative mechanisms of each category are discussed. Building on the established diverse strategies, one can foresee that more innovative and structurally creative magnesium catalysts that are generated in situ will be developed to overcome more formidable challenges of catalytic enantioselective reactions.1 Introduction2 Magnesium Catalysts Generated in Situ from Chiral Ligands Containing Dual Reactive Hydrogens3 Magnesium Catalysts Generated in Situ from Monoanionic Chiral Ligands4 Bimetallic and Polymetallic Magnesium Catalysts Assembled in Situ5 Summary and Outlook


2020 ◽  
Vol 289 ◽  
pp. 121485
Author(s):  
Song Zhang ◽  
Lu Wang ◽  
Yun-Long Tai ◽  
Yun-Lei Teng ◽  
Juan Zhao ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 329
Author(s):  
Chenxi Li ◽  
Jin Cheng ◽  
Qing Ye ◽  
Fanwei Meng ◽  
Xinpeng Wang ◽  
...  

The poisoning effects of alkali metals (K and Na) and alkaline earth metals (Ca and Mg) on catalytic performance of the 2Nb4Ce/Zr-PILC catalyst for the selective catalytic reduction of NOx with NH3 (NH3-SCR) were investigated, and physicochemical properties of the catalysts were characterized by means of the X-ray diffraction XRD (XRD), Brunner−Emmet−Teller (BET), hydrogen temperature-programmed reduction (H2-TPR), X-ray Photoelectron Spectroscopy (XPS), ammonia temperature-programmed desorption (NH3-TPD), and in situ diffuse reflectance infrared Fourier transform spectroscopy (in situ DRIFTS) techniques. Doping of M (M = K, Na, Ca, and Mg) deactivated the 2Nb4Ce/Zr-PILC catalyst according to the sequence of 0.8 K > 0.8 Na > 0.8 Ca > 0.8 Mg (M/Ce molar ratio = 0.8). The characterization results showed that the decreases in redox ability, NH3 adsorption, Ce3+/Ce4+ atomic ratio, and amount of the chemisorbed oxygen (Oβ) were the important factors influencing catalytic activities of the alkali metal-and alkaline earth metal-doped samples. Consequently, compared with the Mg- and Ca-doped samples, doping of K caused the 2Nb4Ce/Zr-PILC sample to possess the lowest redox ability, NH3 adsorption, and amount of the Oβ species, which resulted in an obvious deactivation effect.


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