Catalytic activity of silica supported sulfated zirconia catalysts for liquid phase etherification of C6 olefins with alcohols

2003 ◽  
Vol 84 (1-3) ◽  
pp. 135-146 ◽  
Author(s):  
Shaobin Wang ◽  
James A. Guin
2002 ◽  
Vol 4 (13) ◽  
pp. 3136-3145 ◽  
Author(s):  
C. Morterra ◽  
G. Cerrato ◽  
S. Ardizzone ◽  
C. L. Bianchi ◽  
M. Signoretto ◽  
...  

1998 ◽  
Vol 520 ◽  
Author(s):  
D.W. Matson ◽  
J.G. Darab ◽  
T.D. Brewer ◽  
P.D. Kaviratna

ABSTRACTNanocrystalline sulfated zirconia catalysts were prepared using the rapid thermal decomposition of precursors in solution (RTDS) powder formation process. Zirconia gel formation, initial crystallization, and sulfate incorporation occurred during a brief exposure to hydrothermal conditions in the RTDS reactor. The partially crystalline zirconia solid was collected as a suspension, separated by centrifugation, and subjected to calcination to achieve full catalytic activity. Crystallinity, sulfate content, and catalytic activity of the calcined powders toward butane isomerization varied according to the hydrothermal conditions at which the zirconia powders were originally precipitated. The powders were characterized using powder XRD, FTIR, and XAS.


2007 ◽  
Vol 72 (7) ◽  
pp. 679-686 ◽  
Author(s):  
Aleksandra Zarubica ◽  
Paula Putanov ◽  
Goran Boskovic

Two series of sulfated zirconia catalysts were synthesized from various precursors using mono- or multi-step sequence preparations under laboratory conditions. Their activities/selectivities in the isomerization reaction of n-hexane were correlated to their textural, structural and morphological properties. The slightly higher activity of a commercially sulfated Zr(OH)4-based catalyst is in agreement with the differences in the content of SO24 - ions and their thermal stability, textural and structural properties, i.e., crystallite size and possible imperfection of the incorporation of sulfate groups in the multi-step synthesis of the catalyst having a nitrate origin. The employment of H2 as the carrier gas resulted in no catalytic activity, regardless of the catalyst precursor, preparation method and calcination temperature. When the isomerization reaction was performed under He, the relatively short life-times of all catalyst samples were caused by fast deactivation due to coking in the absence of H2. .


2021 ◽  
Vol 21 (3) ◽  
pp. 163-169
Author(s):  
M. D. Smolikov ◽  
L. I. Bikmetova ◽  
K. V. Kazantsev ◽  
I. V. Muromtsev ◽  
A. S. Belyi

The study considers the effect of iron and manganese introduction on the textural characteristics and phase composition of the alumina matrix used as a support for sulfated zirconia catalysts in hexane isomerization. The additives introduced during plasticization of aluminum hydroxide essentially enhance the catalytic activity, which is expressed in terms of hexane conversion, and the selectivity of isomerization toward the formation of hexane isomers. The distinctive feature of the doped catalysts is the formation of acid sites with LAS/BAS ≥ 2, which promote an increase in the yield of isomers and particularly the yield of high-octane 2,2-dimethylbutane.


2004 ◽  
Vol 227 (2) ◽  
pp. 470-478 ◽  
Author(s):  
S. Ardizzone ◽  
C.L. Bianchi ◽  
G. Cappelletti ◽  
F. Porta

2008 ◽  
Vol 59 (3) ◽  
pp. 292-296
Author(s):  
Mihaiela Ropot ◽  
Emilian Angelescu ◽  
Rodica Zavoianu ◽  
Rodica Birjega

In the preparation of sulfated zirconia catalysts, the properties of products, including catalytic activity, are influenced by the precursor from which Zr(OH)4 is obtained, by agents of precipitation and solvents. The most active catalysts for the isomerization of n-butane to izobutane was obtained from ZrCl4 precipitated with N2H4 . H2O and maturated, but a better selectivity was obtained when ZrOCl2�8H2O was using.


1994 ◽  
Vol 26 (3-4) ◽  
pp. 339-344 ◽  
Author(s):  
F. Pinna ◽  
M. Signoretto ◽  
G. Strukul ◽  
G. Cerrato ◽  
C. Morterra

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