Methanol Usage in Toluene Methylation with Medium and Large Pore Zeolites

被引:71
作者
Ahn, John H. [1 ]
Kolvenbach, Robin [1 ]
Al-Khattaf, Sulaiman S. [2 ]
Jentys, Andreas [1 ]
Lercher, Johannes A. [1 ]
机构
[1] Tech Univ Munich, Dept Chem, D-85747 Garching, Germany
[2] King Fahd Univ Petr & Minerals, Ctr Res Excellence Petr Refining & Petrochem, Dhahran 31261, Saudi Arabia
来源
ACS CATALYSIS | 2013年 / 3卷 / 05期
关键词
toluene methylation; methanol to hydrocarbons; hydrocarbon pool cycle; petrochemical upgrade; acid chemistry in zeolites; CHEMICAL-VAPOR-DEPOSITION; SHAPE-SELECTIVITY; TO-HYDROCARBONS; DIMETHYL ETHER; XYLENE ISOMERIZATION; SURFACE MODIFICATION; ZSM-5; ZEOLITES; ALKYLATION; HZSM-5; CONVERSION;
D O I
10.1021/cs4000766
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The reaction of toluene methylation was investigated with four acidic zeolites of different pore geometries: the medium poke zeolites H-ZSM5 and H-ZSM11 as well as the large pore zeolites H-MOR, and H-BEA. The methylation, Methanol comsumption, light hydrocarbon formation and disproportionation rates for the,reaction of toluene, p-xylene, and 1,2,4-trimethylbenezene with methanol determined: The products of toluene methylation;(e.g. xylenes, and trimethlbenzenes) were readily Methylated further in both, medium and large pore zeolites. A considerably higher fraction of methanol was used to form light hydrocarbons with the medium pore zeolites than with large pore zeolites. This was related to the fact that the dealkylation of light hydrocarbons from highly methylated aromatics became more favorable relative to methylation at an earlier stage, that is, after fewer methyl groups were added to the aromatic ring. Increasing the effective residence time of bulky aromatic molecules with medium pore zeolites, modified either by coating the surface with tetraethyl orthosilicate or by increasing the intracrystal pore length, converted a larger fraction of methanol to light hydrocarbons via methylation and subsequent dealkylation of light hydrocarbons.
引用
收藏
页码:817 / 825
页数:9
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