Alcohol dehydration reactions as chemical precursors for coke formation and acidity probes in tungstated zirconia catalysts

Author(s):  
Gustavo Larsen ◽  
Edgar Lotero ◽  
Mark Nabity ◽  
Lucía Petkovic ◽  
Carlos A. Querini
1997 ◽  
Vol 169 (1) ◽  
pp. 67-75 ◽  
Author(s):  
Gustavo Larsen ◽  
Edgar Lotero ◽  
Lucı́a M. Petkovic ◽  
David S. Shobe

2000 ◽  
Vol 161 (1-2) ◽  
pp. 223-232 ◽  
Author(s):  
P Vázquez ◽  
L Pizzio ◽  
C Cáceres ◽  
M Blanco ◽  
H Thomas ◽  
...  

2008 ◽  
Vol 49 (3-4) ◽  
pp. 259-267 ◽  
Author(s):  
Jose E. Herrera ◽  
Ja Hun Kwak ◽  
Jian Zhi Hu ◽  
Yong Wang ◽  
Charles H. F. Peden

2011 ◽  
Vol 141 (5) ◽  
pp. 649-655 ◽  
Author(s):  
Ja Hun Kwak ◽  
Donghai Mei ◽  
Charles H. F. Peden ◽  
Roger Rousseau ◽  
János Szanyi

2015 ◽  
Vol 2015 ◽  
pp. 1-11
Author(s):  
Heriberto Esteban Benito ◽  
Ricardo García Alamilla ◽  
Juan Manuel Hernández Enríquez ◽  
Francisco Paraguay Delgado ◽  
Daniel Lardizabal Gutiérrez ◽  
...  

Porous silicates were synthesized by a nonhydrothermal method, using sodium silicate as a source of silica and cetyltrimethylammonium bromide as a template agent. Catalysts were characterized using thermogravimetric analysis, N2physisorption, X-ray diffraction, FTIR spectroscopy, pyridine adsorption, potentiometric titration withn-butylamine, scanning electronic microscopy, and transmission electronic microscopy. The surface area of the materials synthesized was greater than 800 m2/g. The introduction of zirconium atoms within the porous silicates increased their acid strength from −42 to 115 mV, while the addition of sulfate ions raised this value to 470 mV. The catalytic activity for the dehydration of alcohols yields conversions of up to 70% for ethanol and 30% for methanol.


2019 ◽  
Author(s):  
Ales Styskalik ◽  
Imene Kordoghli ◽  
Claude Poleunis ◽  
Arnaud Delcorte ◽  
Carmela Aprile ◽  
...  

<div> <p>Herein, we present novel phenylene- and xylylene-bridged silica and metallosilicate materials prepared by non-hydrolytic sol-gel. The hybrid silica are highly porous, chemically similar to periodic mesoporous organosilica (PMO), but amorphous. Analogous hybrid metallosilicates are obtained by directly incorporating Al, Nb, or Sn in the hybrid silica framework. Exhibiting open texture, surface acidity and tunable hydrophobicity, these materials are excellent candidates for catalytic alcohol dehydration reactions. The gas-phase hydrothermal and thermal stability of these materials is examined. While the hybrid silica is expectedly stable, a stark decrease in stability is observed for phenylene bridged silsesquioxanes upon metal introduction. The extent of the hydrolytic Si−C(sp<sup>2</sup>) bond cleavage is quantitatively followed by <sup>29</sup>Si MAS NMR, TG analysis, and GC-FID analysis of effluent coming from samples exposed to water vapor. Two important features affecting the hydrothermal and thermal stability are identified: (i) the homogeneity of metal dispersion within the silica matrix, and (ii) the electronegativity of the incorporated metal. The stability of hybrid metallosilicates is significantly improved by replacing the phenylene bridges with xylylene bridges, due to the presence of more stable Si−C(sp<sup>3</sup>) bonds. Interestingly, the latter hybrid metallosilicate proves to be an active catalyst for the dehydration of ethanol to ethylene. Unlike the other hybrid materials presented here, it reaches high ethylene yields without undergoing degradation and deactivation.</p> </div>


Author(s):  
Ales Styskalik ◽  
Imene Kordoghli ◽  
Claude Poleunis ◽  
Arnaud Delcorte ◽  
Carmela Aprile ◽  
...  

<div> <p>Herein, we present novel phenylene- and xylylene-bridged silica and metallosilicate materials prepared by non-hydrolytic sol-gel. The hybrid silica are highly porous, chemically similar to periodic mesoporous organosilica (PMO), but amorphous. Analogous hybrid metallosilicates are obtained by directly incorporating Al, Nb, or Sn in the hybrid silica framework. Exhibiting open texture, surface acidity and tunable hydrophobicity, these materials are excellent candidates for catalytic alcohol dehydration reactions. The gas-phase hydrothermal and thermal stability of these materials is examined. While the hybrid silica is expectedly stable, a stark decrease in stability is observed for phenylene bridged silsesquioxanes upon metal introduction. The extent of the hydrolytic Si−C(sp<sup>2</sup>) bond cleavage is quantitatively followed by <sup>29</sup>Si MAS NMR, TG analysis, and GC-FID analysis of effluent coming from samples exposed to water vapor. Two important features affecting the hydrothermal and thermal stability are identified: (i) the homogeneity of metal dispersion within the silica matrix, and (ii) the electronegativity of the incorporated metal. The stability of hybrid metallosilicates is significantly improved by replacing the phenylene bridges with xylylene bridges, due to the presence of more stable Si−C(sp<sup>3</sup>) bonds. Interestingly, the latter hybrid metallosilicate proves to be an active catalyst for the dehydration of ethanol to ethylene. Unlike the other hybrid materials presented here, it reaches high ethylene yields without undergoing degradation and deactivation.</p> </div>


Author(s):  
Fabian Beckmann ◽  
Kapil S. Lokare ◽  
Lukas Lätsch ◽  
Christophe Copéret ◽  
Christian Limberg

Author(s):  
Clifford S. Rainey

The spatial distribution of V and Ni deposited within fluidized catalytic cracking (FCC) catalyst is studied because these metals contribute to catalyst deactivation. Y zeolite in FCC microspheres are high SiO2 aluminosilicates with molecular-sized channels that contain a mixture of lanthanoids. They must withstand high regeneration temperatures and retain acid sites needed for cracking of hydrocarbons, a process essential for efficient gasoline production. Zeolite in combination with V to form vanadates, or less diffusion in the channels due to coke formation, may deactivate catalyst. Other factors such as metal "skins", microsphere sintering, and attrition may also be involved. SEM of FCC fracture surfaces, AEM of Y zeolite, and electron microscopy of this work are developed to better understand and minimize catalyst deactivation.


Author(s):  
R. L. Freed ◽  
M. J. Kelley

The commercial introduction of Pt-Re supported catalysts to replace Pt alone on Al2O3 has brought improvements to naphtha reforming. The bimetallic catalyst can be operated continuously under conditions which lead to deactivation of the single metal catalyst by coke formation. Much disagreement still exists as to the exact nature of the bimetallic catalyst at a microscopic level and how it functions in the process so successfully. The overall purpose of this study was to develop the materials characterization tools necessary to study supported catalysts. Specifically with the Pt-Re:Al2O3 catalyst, we sought to elucidate the elemental distribution on the catalyst.


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