Thermodynamic and Mechanistic Analyses of Direct CO2 Methylation with Toluene to para-Xylene.

Abstract

Direct CO2 methylation with toluene, as one of the CO2 hydrogenation technologies, exhibits great potential for the CO2 utilization to produce the valuable para-xylene (PX), but the tandem catalysis remains a challenge for low conversion and selectivity due to the competitive side reactions. The thermodynamic analyses and the comparation with two series of catalytic results of direct CO2 methylation are conducted to investigate the product distribution and possible mechanism in adjusting the feasibility of higher conversion and selectivity. Based on the Gibbs energy minimization method, the optimal thermodynamic conditions for direct CO2 methylation are 360-420 °C, 3 MPa with middle CO2/C7H8 ratio (1:1 to 1:4) and high H2 feed (CO2/H2 = 1:3 to 1:6). As a tandem process, the toluene feed would break the thermodynamic limit and has the higher potential of >60% CO2 conversion than that of CO2 hydrogenation without toluene. The direct CO2 methylation route also has advantages over the methanol route with a good prospect for >90% PX selectivity in its isomers due to the dynamic effect of selective catalysis. These thermodynamic and mechanistic analyses would promote the optimal design of bifunctional catalysts for CO2 conversion and product selectivity from the view of reaction pathways of the complex system.