Synthesis of Spherical Mesoporous Co-MCM-41

2009 ◽  
Vol 79-82 ◽  
pp. 131-134
Author(s):  
Peng Sun ◽  
Yan Kong ◽  
Jun Du ◽  
Xin Jie Xu ◽  
Jun Wang ◽  
...  

A serious of spherical Co-MCM-41s with different cobalt content was synthesized and characterized by XRD, SEM, N2 isotherms and ICP techniques. The influences of synthesis conditions on the structure were also studied. The use of ascorbic acid as reductant had significant influence on the morphology and the catalytic activity of Co-MCM-41. The prepared samples exhibited higher catalytic activity in the direct hydroxylation of benzene by H2O2 than those with common morphology.

2016 ◽  
Vol 55 (14) ◽  
pp. 3900-3908 ◽  
Author(s):  
Milad Jourshabani ◽  
Alireza Badiei ◽  
Zahra Shariatinia ◽  
Negar Lashgari ◽  
Ghodsi Mohammadi Ziarani

2013 ◽  
Vol 100 ◽  
pp. 159-162 ◽  
Author(s):  
Bing Han ◽  
Haiqing Wang ◽  
Yan Kong ◽  
Jun Wang

RSC Advances ◽  
2016 ◽  
Vol 6 (90) ◽  
pp. 87656-87664 ◽  
Author(s):  
Liya Hu ◽  
Cheng Wang ◽  
Bin Yue ◽  
Xueying Chen ◽  
Heyong He

The integration of highly dispersed V species and NC support with superior properties endows xV/NC-y catalysts with excellent catalytic activity.


2019 ◽  
Vol 9 (3) ◽  
pp. 811-821 ◽  
Author(s):  
Zhao-Meng Wang ◽  
Li-Juan Liu ◽  
Bo Xiang ◽  
Yue Wang ◽  
Ya-Jing Lyu ◽  
...  

The catalytic activity decreases as –(SiO)3Mo(OH)(O) > –(SiO)2Mo(O)2 > –(O)4–MoO.


Author(s):  
Mohsen Nikoorazm ◽  
Maryam Khanmoradi ◽  
Masoumeh Sayadian

Introduction:: MCM-41 was synthesized using the sol-gel method. Then two new transition metal complexes of Nickel (II) and Vanadium (IV), were synthesized by immobilization of adenine (6-aminopurine) into MCM-41 mesoporous. The compounds have been characterized by XRD, TGA, SEM, AAS and FT-IR spectral studies. Using these catalysts provided an efficient and enantioselective procedure for oxidation of sulfides to sulfoxides and oxidative coupling of thiols to their corresponding disulfides using hydrogen peroxide at room temperature. Materials and Methods:: To a solution of sulfide or thiol (1 mmol) and H2O2 (5 mmol), a determined amount of the catalyst was added. The reaction mixture was stirred at room temperature for the specific time under solvent free conditions. The progress of the reaction was monitored by TLC using n-hexane: acetone (8:2). Afterwards, the catalyst was removed from the reaction mixture by centrifugation and, then, washed with dichloromethane in order to give the pure products. Results:: All the products were obtained in excellent yields and short reaction times indicating the high activity of the synthesized catalysts. Besides, the catalysts can be recovered and reused for several runs without significant loss in their catalytic activity. Conclusion:: These catalytic systems furnish the products very quickly with excellent yields and VO-6AP-MCM-41 shows high catalytic activity compared to Ni-6AP-MCM-41.


2012 ◽  
Vol 463-464 ◽  
pp. 189-193
Author(s):  
Kong Zhai Li ◽  
Masaaki Haneda ◽  
Masakuni Ozawa

Maghemite (γ-FeSubscript text2OSubscript text3) and hematite (α-Fe2O3) nanoparticles with various dominant exposure crystal planes were prepared by several different methods. The structure and the reducibility of these materials were investigated by XRD, Raman and H2-TPR technologies, and their catalytic performance for propene oxidation was also discussed. The maghemite (γ-FeSubscript text2OSubscript text3) showed a better reducibility than hematite (α-FeSubscript text2OSubscript text3), but its activity for propene oxidation is relatively lower. The exposure crystal plane of hematite has a significant influence on its catalytic activity for propene oxidation. Among the prepared four samples, the hematite-1 sample showed the best activity. The selective growth of any planes with a relative low density of Fe atoms for the α-FeSubscript text2OSubscript text3 catalyst would lead to an obvious decrease in the catalytic activity.


1996 ◽  
Vol 38 (1-2) ◽  
pp. 33-37 ◽  
Author(s):  
Xiu S. Zhao ◽  
Gao Q. Lu ◽  
Graeme J. Millar ◽  
Xin S. Li

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