Study of mayenite produced from waste eggshell as support for Ni-Co catalysts for biomass tar cracking

Author(s):  
Christian Manera ◽  
Daniele Perondi ◽  
Guilherme Luiz Dotto ◽  
Thiago Barcellos ◽  
Marcelo Godinho
2015 ◽  
Vol 54 (21) ◽  
pp. 5613-5623 ◽  
Author(s):  
Elmer B. Ledesma ◽  
Alyssa A. Mullery ◽  
Jacqueline V. Vu ◽  
Jennifer N. Hoang

RSC Advances ◽  
2018 ◽  
Vol 8 (71) ◽  
pp. 40873-40882 ◽  
Author(s):  
Qing Dong ◽  
Huaju Li ◽  
Shuping Zhang ◽  
Xiangqian Li ◽  
Wa Zhong

We explored the effect of Ni/RHC catalyst on tar removal and syngas production under microwave conditions.


2021 ◽  
Vol 218 ◽  
pp. 106858
Author(s):  
Sisi Huang ◽  
Hailiang Xu ◽  
Hongyan Li ◽  
Yifeng Guo ◽  
Zhenjie Sun ◽  
...  

Fuel ◽  
2013 ◽  
Vol 112 ◽  
pp. 654-661 ◽  
Author(s):  
Lei Wang ◽  
Dalin Li ◽  
Mitsuru Koike ◽  
Hideo Watanabe ◽  
Ya Xu ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (101) ◽  
pp. 82845-82852 ◽  
Author(s):  
Yebing Mao ◽  
Yuping Dong ◽  
Bin Wang ◽  
Jiafu Chang ◽  
Jie Yu ◽  
...  

A novel apparatus called micro fluidized bed reactor for liquids exhibits eligibility and superiority for analyzing reactions of liquid samples.


2019 ◽  
Author(s):  
Ke-Yin Ye ◽  
Terry McCallum ◽  
Song Lin

Organic radicals are generally short-lived intermediates with exceptionally high reactivity. Strategically, achieving synthetically useful transformations mediated by organic radicals requires both efficient initiation and selective termination events. Here, we report a new catalytic strategy, namely bimetallic radical redox-relay, in the regio- and stereoselective rearrangement of epoxides to allylic alcohols. This approach exploits the rich redox chemistry of Ti and Co complexes and merges reductive epoxide ring opening (initiation) with hydrogen atom transfer (termination). Critically, upon effecting key bond-forming and -breaking events, Ti and Co catalysts undergo proton-transfer/electron-transfer with one another to achieve turnover, thus constituting a truly synergistic dual catalytic system.<br>


2010 ◽  
Vol 31 (10) ◽  
pp. 1281-1285
Author(s):  
Peichao SHI ◽  
Tianhu CHEN ◽  
Xianlong ZHANG ◽  
Dong CHEN ◽  
Lei SONG ◽  
...  
Keyword(s):  

2020 ◽  
Vol 01 ◽  
Author(s):  
Bonamali Pal ◽  
Anila Monga ◽  
Aadil Bathla

Background:: Bimetallic nanocomposites have currently gained significant importance for enhanced catalytic applications relative to monometallic analogues. The synergistic interactions modified electronic and optical properties in the bimetallic (M1@M2) structural morphology e.g., core-shell /alloy nanostructures resulted in a better co-catalytic performance for TiO2 photocatalysis. Objective:: Hence, this article discusses the preparation, characterization, and co-catalytic activity of different bimetallic nanostructures namely, Cu@Zn, Pd@Au, Au@Ag, and Ag@Cu, etc. Method:: These bimetallic co-catalysts deposited on TiO2 possess the ability to absorb visible light due to surface plasmonic absorption and are also expected to display the new properties due to synergy between two distinct metals. As a result, they reveal the highest level of activity than the monometal deposited TiO2. Result:: Their optical absorption, emission, charge carrier dynamics, and surface structural morphology are explained for the improved photocatalytic activity of M1@M2 loaded TiO2 for the hydrogenation of certain organic compounds e.g., quinoline, crotonaldehyde, and 1,3-dinitrobenzene, etc. under UV/ visible light irradiation. Conclusion:: It revealed that the use of bimetallic core@shell co-catalyst for hydrogenation of important industrial organics by M1@M2-TiO2 nanocomposite demonstrates beneficial reactivity in many instances relative to conventional transition metal catalysts.


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