Enhancing high selectivity production of light aromatics from in-situ catalytic upgrading of cellulose pyrolysis vapors by regulating hierarchical core-shell ZSM-5@MCM-41

摘要

The catalytic upgrading of cellulose pyrolysis vapors is one of the effective methods to realize its high value utilization. Tuning the pore structure and acid sites of ZSM-5 (Z5) is a necessary strategy to develop effective catalysts for the production of light aromatics and the inhibition of carbon formation. In this study, a core-shell structure ZSM-5 @MCM-41 was developed and used for the first time in catalytic fast pyrolysis (CFP) of cellulose to prepare light aromatic hydrocarbons. The successful synthesis of the hierarchical core-shell ZSM-5 @MCM-41 was confirmed by nitrogen physisorption, X-ray diffraction (XRD), and transmission electron microscope (TEM) analysis. In aromatic hydrocarbon production, 1.0SH-Z5 @ M41 (1.0 mol/L, ZSM-5 @MCM-41) has the highest relative content of 98.76. The relative content of BTEX (benzene, toluene, ethylbenzene, and xylene) is up to 89.83, which is 2.39 times that of traditional microporous Z5. The quadratic polynomials were developed to correlate the Bronsted-to-Lewis acid site strength ratio (BLR) and mesopore-to-micropore volume ratio (MMR) with the relative content of BTEX. The mechanism of in-situ catalytic upgrading of cellulose pyrolysis vapor over ZSM-5 @MCM-41 was revealed. Due to high selectivities and low coke formation, ZSM-5 @MCM-41 offers an improved option for making monocyclic aromatics from cellulosic biomass.