Catalytic Activity of ZSM-22 Zeolites in the Skeletal Isomerization Reaction of 1-Butene

1997 ◽  
Vol 36 (8) ◽  
pp. 2990-2995 ◽  
Author(s):  
Rune Byggningsbacka ◽  
Lars-Eric Lindfors ◽  
Narendra Kumar
2012 ◽  
Vol 4 (2) ◽  
pp. 141-149 ◽  
Author(s):  
A. A. Lamberov ◽  
E. Yu. Sitnikova ◽  
I. N. Mukhambetov ◽  
R. F. Zalyaliev ◽  
R. R. Gil’mullin ◽  
...  

2019 ◽  
Vol 9 (17) ◽  
pp. 4505-4509
Author(s):  
Wenhan Chen ◽  
Guilong Qiao ◽  
Huijing Liu ◽  
Songshou Ye ◽  
Jinbao Zheng ◽  
...  

Site shifting by templated coordination aimed at enhancing the performance during n-butene skeletal isomerization under severe conditions.


2005 ◽  
Vol 225 (1) ◽  
pp. 39-46 ◽  
Author(s):  
Lúcia K. Noda ◽  
Rusiene M. de Almeida ◽  
Luiz Fernando D. Probst ◽  
Norberto S. Gonçalves

RSC Advances ◽  
2015 ◽  
Vol 5 (96) ◽  
pp. 78441-78447 ◽  
Author(s):  
Phan Huy Hoang ◽  
Bach Nguyen Xuan

The magnetically recyclable ZSM-5 zeolite (MZZ) with high catalytic activity, high efficiency in separation, recycling and long lifetime for epoxide isomerization reaction was presented.


1999 ◽  
Vol 183 (2) ◽  
pp. 345-356 ◽  
Author(s):  
Carlos Moreno-Castilla ◽  
Francisco José Maldonado-Hódar ◽  
José Rivera-Utrilla ◽  
Enrique Rodrı́guez-Castellón

2011 ◽  
Vol 233-235 ◽  
pp. 234-237 ◽  
Author(s):  
Sa Liu ◽  
Jian Wei Guo ◽  
Chu Fen Yang ◽  
Long Huan Li ◽  
Yi Hua Cui

Al-containing mesoporous molecular sieves(Al-MCM-41) were synthesized at ambient temperature. The structures of samples were characterized by XRD, N2-adsorption/desorption isotherms and FT-IR, etc. The evaluation results showed that Al-MCM-41 had higher catalytic activity for isomerization conversion of endo-tetrahydrodicyclo-pentadiene (endo-TCD) into exo-tetrahydrodicyclo-pentadiene (exo-TCD) and adamantane (AdH). Loading inorganic acid on the surface of Al-MCM-41 led increase of its catalytic activity and the yield of adamantane.


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. .


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