Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
School of Chemical Science, University of Chinese Academy of Sciences, Beijing, China.
Nat Commun. 2021 Jul 26;12(1):4534. doi: 10.1038/s41467-021-24780-8.
Benzene is a widely used commodity chemical, which is currently produced from fossil resources. Lignin, a waste from lignocellulosic biomass industry, is the most abundant renewable source of benzene ring in nature. Efficient production of benzene from lignin, which requires total transformation of C-C/C-O into C-H bonds without side hydrogenation, is of great importance, but has not been realized. Here, we report that high-silica HY zeolite supported RuW alloy catalyst enables in situ refining of lignin, exclusively to benzene via coupling Bronsted acid catalyzed transformation of the C-C bonds on the local structure of lignin molecule and RuW catalyzed hydrogenolysis of the C-O bonds using the locally abstracted hydrogen from lignin molecule, affording a benzene yield of 18.8% on lignin weight basis in water system. The reaction mechanism is elucidated in detail by combination of control experiments and density functional theory calculations. The high-performance protocol can be readily scaled up to produce 8.5 g of benzene product from 50.0 g lignin without any saturation byproducts. This work opens the way to produce benzene using lignin as the feedstock efficiently.
苯是一种广泛使用的商品化学品,目前主要从化石资源中生产。木质素是木质纤维素生物质工业的一种废物,是自然界中苯环最丰富的可再生资源。高效地从木质素生产苯需要将 C-C/C-O 键完全转化为 C-H 键,而不发生侧加氢,这非常重要,但尚未实现。在这里,我们报告高硅 HY 沸石负载的 RuW 合金催化剂能够原位精制木质素,通过在木质素分子的局部结构上进行的布朗斯台德酸催化的 C-C 键转化以及从木质素分子中局部提取的氢进行的 RuW 催化氢解,仅将其转化为苯,在水体系中以木质素重量为基准,苯的收率为 18.8%。通过对照实验和密度泛函理论计算的结合,详细阐明了反应机理。该高性能方案可以很容易地扩大规模,从 50.0g 木质素中生产 8.5g 苯,而没有任何饱和副产物。这项工作为使用木质素作为原料高效生产苯开辟了道路。