Hierarchical composite catalysts of MCM-41 on zeolite Beta for conversion of heavy reformate to xylenes

2021 ◽  
Vol 98 ◽  
pp. 189-199
Author(s):  
Syed A. Ali ◽  
Faisal M. Almulla ◽  
B. Rabindran Jermy ◽  
Abdullah M. Aitani ◽  
Raed H. Abudawoud ◽  
...  
2005 ◽  
Vol 12 (3) ◽  
pp. 193-199 ◽  
Author(s):  
Valeri Naydenov ◽  
Lubomira Tosheva ◽  
Johan Sterte
Keyword(s):  

2007 ◽  
Vol 15 (2) ◽  
pp. 133-138 ◽  
Author(s):  
Yuping Li ◽  
Wei Zhang ◽  
Xiaoli Wang ◽  
Ying Zhang ◽  
Tao Dou ◽  
...  

2008 ◽  
Vol 20 (16) ◽  
pp. 5122-5124 ◽  
Author(s):  
John C. McKeen ◽  
Yushan S. Yan ◽  
Mark E. Davis

2001 ◽  
Vol 11 (7) ◽  
pp. 1886-1890 ◽  
Author(s):  
Wanping Guo ◽  
Chunrong Xiong ◽  
Limin Huang ◽  
Quanzhi Li

2007 ◽  
Vol 72 (5-6) ◽  
pp. 728-746 ◽  
Author(s):  
Martina Bejblová ◽  
Josef Vlk ◽  
Dana Procházková ◽  
Helena Šiklová ◽  
Jiří Čejka

The role of the type of acid site (Broensted vs. Lewis) on the activity and selectivity of molecular sieve catalysts was investigated in ferrocene and toluene acylation. H-, Zn-, Fe-, Al- and La-forms of zeolite Beta, USY and mesoporous molecular sieves (Al)MCM-41, (Al)SBA-15 were tested. It was observed that addition of metal cations acting as Lewis acid sites can increase the acidity of various molecular sieve catalysts. No general relationship between the type of cation and conversion of individual substrate was found. While the highest activity in ferrocene acylation was observed after addition of Zn, in the case of toluene acylation Al-forms of catalysts were the most active. The results indicate that the acid strength of cationic Lewis sites controls their activity in acylation reactions.


2005 ◽  
Vol 70 (11) ◽  
pp. 1829-1847 ◽  
Author(s):  
Pavla Prokešová ◽  
Nikolay Petkov ◽  
Jiří Čejka ◽  
Svetlana Mintova ◽  
Thomas Bein

Composite materials containing micro- and mesopores are prepared under instantaneous hydrothermal treatment of initial solutions generally used for zeolite Beta and precursor solutions for mesoporous Al-MCM-41 material. The resulting composites are compared with pure, highly crystalline colloidal microporous Beta zeolite and hexagonally ordered mesostructured samples. The porosity and morphological features of the composite materials are influenced by the conditions of hydrothermal synthesis of the initial colloidal solutions used for the preparation of Beta seeds, as well as by the conditions of the synchronized crystallization of the final composites. The embedding of Beta seeds in the mesoporous silica matrix is possible via immediate heating of mesoporous precursor solutions with Beta seeds primarily formed. The composite materials contain either microcrystalline Beta nanodomains with sizes of about 5-10 nm surrounded by mesoporous material or defined Beta nanocrystals (20-40 nm), and at the same time connected with mesostructured material. The presence of highly crosslinked silicate framework walls and tetrahedrally coordinated aluminum in the composite material are confirmed by solid-state 29Si and 27Al MAS NMR spectroscopy. The concentration of Brønsted acid sites in the micro/mesoporous composites is increased substantially in comparison with pure mesoporous Al-MCM-41 material proven by FTIR acetonitrile-d3 adsorption study.


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