Ti-YNU-2: A Microporous Titanosilicate with Enhanced Catalytic Performance for Phenol Oxidation

ACS Catalysis ◽  
2014 ◽  
Vol 4 (8) ◽  
pp. 2653-2657 ◽  
Author(s):  
Makiko Sasaki ◽  
Yuya Sato ◽  
Yasuyuki Tsuboi ◽  
Satoshi Inagaki ◽  
Yoshihiro Kubota
RSC Advances ◽  
2019 ◽  
Vol 9 (15) ◽  
pp. 8463-8479 ◽  
Author(s):  
Zenaida Guerra-Que ◽  
Hermicenda Pérez-Vidal ◽  
G. Torres-Torres ◽  
Juan Carlos Arévalo-Pérez ◽  
Adib Abiu Silahua Pavón ◽  
...  

Influence of the calcination and reduction treatment effects used to activate catalysts on the global catalytic performance on phenol oxidation over different supports.


1996 ◽  
Vol 58 (1) ◽  
pp. 105-110 ◽  
Author(s):  
L. V. Pirutko ◽  
K. A. Dubkov ◽  
L. P. Solovyeva ◽  
G. I. Panov

Zeolites ◽  
1995 ◽  
Vol 15 (3) ◽  
pp. 253-258 ◽  
Author(s):  
A.S. Kharitonov ◽  
V.B. Fenelonov ◽  
T.P. Voskresenskaya ◽  
N.A. Rudina ◽  
V.V. Molchanov ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (39) ◽  
pp. 32789-32797 ◽  
Author(s):  
Lei Luo ◽  
Chengyi Dai ◽  
Anfeng Zhang ◽  
Junhu Wang ◽  
Chunshan Song ◽  
...  

Facile modification of FeZSM-5 utilizing an organic directing agent (ODA) for iron species evolution toward better Fenton activity was developed.


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.


2020 ◽  
Vol 8 (35) ◽  
pp. 18207-18214
Author(s):  
Dongbo Jia ◽  
Lili Han ◽  
Ying Li ◽  
Wenjun He ◽  
Caichi Liu ◽  
...  

A novel, rational design for porous S-vacancy nickel sulfide catalysts with remarkable catalytic performance for alkaline HER.


2019 ◽  
Author(s):  
M. Alexander Ardagh ◽  
Manish Shetty ◽  
Anatoliy Kuznetsov ◽  
Qi Zhang ◽  
Phillip Christopher ◽  
...  

Catalytic enhancement of chemical reactions via heterogeneous materials occurs through stabilization of transition states at designed active sites, but dramatically greater rate acceleration on that same active site is achieved when the surface intermediates oscillate in binding energy. The applied oscillation amplitude and frequency can accelerate reactions orders of magnitude above the catalytic rates of static systems, provided the active site dynamics are tuned to the natural frequencies of the surface chemistry. In this work, differences in the characteristics of parallel reactions are exploited via selective application of active site dynamics (0 < ΔU < 1.0 eV amplitude, 10<sup>-6</sup> < f < 10<sup>4</sup> Hz frequency) to control the extent of competing reactions occurring on the shared catalytic surface. Simulation of multiple parallel reaction systems with broad range of variation in chemical parameters revealed that parallel chemistries are highly tunable in selectivity between either pure product, even when specific products are not selectively produced under static conditions. Two mechanisms leading to dynamic selectivity control were identified: (i) surface thermodynamic control of one product species under strong binding conditions, or (ii) catalytic resonance of the kinetics of one reaction over the other. These dynamic parallel pathway control strategies applied to a host of chemical conditions indicate significant potential for improving the catalytic performance of many important industrial chemical reactions beyond their existing static performance.


2014 ◽  
Vol 29 (2) ◽  
pp. 124-130 ◽  
Author(s):  
Yu-Cheng DU ◽  
Guang-Wei ZHENG ◽  
Qi MENG ◽  
Li-Ping WANG ◽  
Hai-Guang FAN ◽  
...  

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