Xylene Synthesis Through Tandem CO2 Hydrogenation and Toluene Methylation Over a Composite ZnZrO Zeolite Catalyst

Selective synthesis of specific value-added aromatics from CO2 hydrogenation is of paramount interest for mitigating energy and climate problems caused by CO2 emission. Herein, we report a highly active composite catalyst of ZnZrO and HZSM-5 (ZZO/Z5-SG) for xylene synthesis from CO2 hydrogenation via a coupling reaction in the presence of toluene, achieving a xylene selectivity of 86.5 % with CO2 conversion of 10.5 %. A remarkably high space time yield of xylene could reach 215 mg g(cat)(-1) h(-1), surpassing most reported catalysts for CO2 hydrogenation. The enhanced performance of ZZO/Z5-SG could be due to high dispersion and abundant oxygen vacancies of the ZZO component for CO2 adsorption, more feasible hydrogen activation and transfer due to the close interaction between the two components, and enhanced stability of the formate intermediate. The consumption of methoxy and methanol from the deep hydrogenation of formate by introduced toluene also propels an oriented conversion of CO2.

Automated summary

A highly active composite catalyst (ZZO/Z5-SG) of ZnZrO and HZSM-5 was reported for xylene synthesis from CO2 hydrogenation in the presence of toluene, achieving a xylene selectivity of 86.5% and CO2 conversion of 10.5%. The catalyst exhibited a remarkably high space time yield of xylene (215 mg g(cat)(-1) h(-1)), surpassing most reported catalysts for CO2 hydrogenation. The enhanced performance of ZZO/Z5-SG could be attributed to high dispersion and abundant oxygen vacancies of ZZO for CO2 adsorption, close interaction between the two components for more feasible hydrogen activation and transfer, and enhanced stability of the formate intermediate.