Regulating anisotropic diffusion in zeolite for reinforced para-xylene synthesis via CO2 hydrogenation in the presence of toluene

Xin Shang, Jingfeng Han, Qiao Han, Guangjin Hou, Anmin Zheng, Xiaofeng Yang, Zhiqiang Liu, Guodong Liu, Xiong Su, Yanqiang Huang, Tao Zhang
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Abstract

The synthesis of valuable aromatics via CO transformation, especially -xylene (PX), is of paramount significance but still remains greatly challenging due to the low efficiency and poor selectivity. The present work utilized a composite catalyst based on ZnZrO with a modified H-ZSM-5 exhibiting nano-prism stacking to realize the selective synthesis of PX. Methoxy species generated from CO-derived formate produced as an intermediate over the ZnZrO were readily incorporated into the xylene products for effective alkylation, contributed to an enhanced aromatics-based cycle that provided a selectivity for xylenes among all C hydrocarbons of 91.1 %. The lengthened straight channels in the H-ZSM-5 along the -axis, derived from the crystal stacking pattern, increased differences in the diffusion properties of the xylene isomers, and thereby steering the movement of molecules toward a product shape-selective pathway, leading to 90.1 % selectivity for PX among all xylenes, and provided exceptional CO utilization efficiency of ∼60 %.
调节沸石中的各向异性扩散,在甲苯存在下通过二氧化碳加氢强化对二甲苯的合成
通过一氧化碳转化合成有价值的芳烃,尤其是二甲苯(PX),具有极其重要的意义,但由于效率低、选择性差,仍面临巨大挑战。本研究利用一种基于 ZnZrO 和具有纳米棱柱堆叠的改性 H-ZSM-5 的复合催化剂来实现 PX 的选择性合成。在 ZnZrO 上作为中间体产生的甲酸一氧化碳生成的甲氧基物种很容易与二甲苯产物结合以进行有效的烷基化,从而促进了基于芳烃的增强型循环,在所有碳氢化合物中对二甲苯的选择性达到 91.1%。H-ZSM-5 中沿 - 轴的加长直通道源自晶体堆叠模式,它增加了二甲苯异构体扩散特性的差异,从而引导分子向产品形状选择性路径移动,在所有二甲苯中,对 PX 的选择性达到 90.1%,并提供了高达 60% 的优异 CO 利用效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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