journal article·2024-11-20

Advanced Synthesis of Hierarchically Porous Zeolite Catalysts Utilizing Biomass Templates for the Catalytic Pyrolysis of Stearic Acid into Short-Chain Olefins

Yiling Wu, Yikun Zhou, Kok Bing Tan, Youting Wang, Kaiji Xu, Xinyi Zheng, Kaixuan Li, Jian Tian, Xiaoping Rao, Guowu Zhan

ACS Applied Materials & Interfaces· Volume 16· Issue 46
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Abstract

In this study, hierarchically porous ZSM-5 catalysts were fabricated by one-pot assembling ZSM-5 particles onto diverse biomass templates (e.g., rice husk, tea seed husk, tung shell, and coconut shell), wherein the biomass template was transformed into bio-SiO 2 or biochar depending on the calcination conditions. The biotemplated ZSM-5 variants, including ZSM-5(RH), ZSM-5(TSH), ZSM-5(TS), and ZSM-5(CS), exhibited significantly improved deoxygenation performance, achieving ∼100.0% deoxygenation efficiency as compared to the untemplated ZSM-5 catalyst (85.3%). Among them, the ZSM-5(TSH) catalyst exhibited the best performance, accompanied by 100% conversion, 99.6% deoxygenation rate, and 82.3% olefin selectivity. Interestingly, the product distribution over biotemplated ZSM-5 was dominant C 4 = -C 8 = (selectivity of ∼100% in total olefins), while long-chain olefins (C 9 = -C 17 = ) was the major product (selectivity of 57.3%) over the untemplated ZSM-5. Moreover, molecular dynamics (MD) simulations revealed that biotemplated ZSM-5 exhibited superior diffusion coefficients of stearic acid (reaction substrate) and anthracene (coke precursor) compared to the untemplated ZSM-5, indicating higher self-diffusion rates and consequently superior activity and stability in the catalytic pyrolysis reactions. Furthermore, in situ DRIFTS results showed stearic acid over ZSM-5(TSH) primarily was converted to the C 17 H 36 intermediate mainly via the decarboxylation route, followed by dehydrogenation pyrolysis and C–C breaking reactions into C 4 = -C 8 = products. Overall, this work developed an effective strategy for manufacturing hierarchically porous zeolite catalysts using biomass-derived bio-SiO 2 or biochar as the platform.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Zeolite Catalysis and Synthesis · Catalysis and Hydrodesulfurization Studies · Catalysis for Biomass Conversion

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Academy of Advanced Carbon Conversion Technology, College of Chemical Engineering, Huaqiao University, 668 Jimei Avenue, Xiamen, Fujian 361021, P. R. China

Fujian Provincial Key Laboratory of Biomass Low-Carbon Conversion, Huaqiao University, 668 Jimei Avenue, Xiamen, Fujian 361021, P. R. China

Funding

National Natural Science Foundation of China

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