Mobil xylene isomerization process

Author(s):  
B. Cornils
2017 ◽  
Vol 46 (30) ◽  
pp. 9934-9950 ◽  
Author(s):  
Kinga Gołąbek ◽  
Karolina A. Tarach ◽  
Kinga Góra-Marek

This study attempts to offer an insight into o-xylene isomerization process in terms of steric constraints of 10-ring zeolites.


2008 ◽  
Vol 73 (8-9) ◽  
pp. 1061-1088
Author(s):  
Sule Rabiu ◽  
Sulaiman Al-Khattaf

In this work three important aromatic transformations, namely: toluene disproportionation, toluene methylation and m-xylene isomerization, were investigated in a riser simulator which closely mimics the operation of commercial fluidized bed reactors. The transformations were studied over a ZSM-5 based catalyst with medium acidity of 0.23 mmol/g and a series of Y zeolites of acidities between 0.55 and 0.03 mmol/g. For pure toluene feed, it was observed that conversion over the ZSM-5 based catalyst and the weakly acidic Y zeolite (USY-1) was very low. However, with the highly acidic Y zeolite (H-Y), significant toluene conversion was observed with paring reaction more prominent than disproportionation. On the other hand, when toluene was alkylated with methanol, higher toluene conversions were achieved over both the ZSM-5 based and the weakly acidic USY-1 catalysts as compared to when pure toluene feed was used. In addition, p-xylene/o-xylene (P/O) ratios higher than the equilibrium values were obtained in the reaction product over both catalysts. Finally, for m-xylene isomerization it was found that m-xylene conversion increased initially as the acidity of the catalyst increased up to 0.1 mmol/g beyond which any further increase in acidity resulted in a slight decrease in the m-xylene conversion.


Author(s):  
Lei Miao ◽  
Zhe Hong ◽  
Guoqing Zhao ◽  
Fangtao Huang ◽  
Zhirong Zhu

Mo/ZSM-5 catalysts of xylene isomerization were prepared on the intergrowth ZSM-5 support by impregnation-calcination-reduction procedure. ZSM-5 zeolite with intergrowth crystals was prepared for high shape selectivity by the hydrothermal method....


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