Enhanced conversion of lignin into mono-cycloalkanes via C–C bonds cleavage over multifunctional Pt-Nb/MOR catalyst

IF 15.7 1区 化学 Q1 CHEMISTRY, APPLIED
Zhiruo Guo, Xiaohui Liu, Yong Guo, Yanqin Wang
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引用次数: 0

Abstract

The efficient conversion of lignin into mono-cycloalkanes via both C–O and C–C bonds cleavage are attractive, but challenging due to the high C–C bond dissociation energy. Previous studies have demonstrated that NbOx-based catalysts exhibited exceptional capabilities for CAr–C bond cleavage and broken the limitation of lignin monomers. In this work, we presented an economical multifunctional Pt-Nb/MOR catalyst that achieved an impressive monomer yield of 147% during the depolymerization and hydrodeoxygenation of lignin into mono-cycloalkanes. Reaction pathway studies showed that unlike traditional NbOx-based catalytic system, bicyclohexane was an important intermediate in this system and followed the Csp3–Csp3 cleavage pathway after complete cyclic-hydrogenation. Deep investigations demonstrated that the doping of Nb in Pt/MOR not only enhanced the activation of hydrogen by Pt, but also increased the acidity of MOR, both of these are favor for the hydrogenolytic cleavage of Csp3–Csp3 bonds. This work provides a low-cost catalyst to obtain high-yield monomers from lignin under relatively mild conditions and would help to design catalysts with higher activity for the valorization of lignin.
在多功能Pt-Nb/MOR催化剂上通过C-C键裂解促进木质素转化为单环烷烃
通过 C-O 和 C-C 键裂解将木质素高效转化为单环烷烃具有吸引力,但由于 C-C 键离解能较高,因此具有挑战性。以往的研究表明,氧化铌基催化剂在 CAr-C 键裂解方面表现出卓越的能力,并打破了木质素单体的限制。在这项工作中,我们提出了一种经济型多功能铂铌/MOR 催化剂,在木质素解聚和加氢脱氧成单环烷的过程中,其单体产率达到了惊人的 147%。反应路径研究表明,与传统的 NbOx 催化体系不同,双环己烷是该体系中的重要中间体,在完全循环氢化后遵循 Csp3-Csp3 裂解路径。深入研究表明,在 Pt/MOR 中掺入 Nb 不仅增强了 Pt 对氢的活化,还提高了 MOR 的酸度,这两者都有利于 Csp3-Csp3 键的氢解裂解。这项研究为在相对温和的条件下从木质素中获得高产单体提供了一种低成本催化剂,并有助于设计出具有更高活性的催化剂来实现木质素的价值化。
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来源期刊
Chinese Journal of Catalysis
Chinese Journal of Catalysis 工程技术-工程:化工
CiteScore
25.80
自引率
10.30%
发文量
235
审稿时长
1.2 months
期刊介绍: The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.
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