Dual-engine-driven realizing high-yield synthesis of Para-Xylene directly from CO 2 -containing syngas.
Xuemei WuChengwei WangShengying ZhaoYang WangTao ZhangJie YaoWeizhe GaoBaizhang ZhangTaiki ArakawaYingluo HeFei ChenMinghui TanGuohui YangNoritatsu TsubakiPublished in: Nature communications (2024)
The direct synthesis of light aromatics, especially para-xylene (p-X), from syngas/CO 2 is drawing strong interest, but improving the space-time yield (STY) of p-X is a significant challenge. Here, a dynamic "dual-engine-driven" (DED) catalytic system is designed by combining two partners of ZnCr and FeMn (named "dual-engine") with Z5@SiO 2 capsule zeolite. The DED catalyst of 1.0%FeMn&[ZnCr&Z5@SiO 2 ] shows an extremely higher p-X STY of 36.1 g p-x ·k gcat -1 ·h -1 , about eight times higher than that of [ZnCr&Z5]. DED manipulates ZnCr engine for methanol formation and drives FeMn engine for light olefins generation together, and then the formed methanol and light olefins are coordinately converted in situ into p-X-rich aromatics over Z5@SiO 2 . The DED model boosts the driving force for syngas/CO 2 conversion, simultaneously concerting the cooperation of "dual-engine" for p-X generation, resulting in extremely high STY of p-X. This study achieves non-petroleum p-X production at industrial-relevant level and advances knowledge in designing innovative heterogeneous catalysts.