木质素
光催化
估价
化学
降级(电信)
烯烃
反应机理
光化学
催化作用
纳米技术
材料科学
化学工程
组合化学
有机化学
废物管理
计算机科学
电信
工程类
作者
Christopher William James Murnaghan,Nathan Skillen,Christopher Hardacre,John Bruce,Gary N. Sheldrake,Peter K. J. Robertson
出处
期刊:JPhys energy
[IOP Publishing]
日期:2021-04-16
卷期号:3 (3): 035002-035002
被引量:10
标识
DOI:10.1088/2515-7655/abf853
摘要
Abstract The valorisation of lignin has gained significant interest in bioenergy, which is driven by the abundance of the material coupled with the potential to form value-added compounds. As a result, the range of technologies deployed for this application has increased and more recently includes advanced oxidation processes such as photocatalysis. The complexity of lignin is challenging however, and therefore model compounds, which represent key linkages in the native structure, have become crucial as both a tool for evaluating novel technologies and for providing an insight into the mechanism of conversion. Previously, the β- O-4 dimer, the most abundant linkage found in native lignin, has been extensively used as a model compound. Described herein, however, is the first report of photocatalytic TiO 2 technology for the degradation of a β- 5 model dimer. Under low power UV-light emitting diode irradiation, complete degradation of the β- 5 compound (6.3 × 10 −3 mg ml −1 min −1 ) was achieved along with formation and subsequent removal of reaction intermediates. Investigation into the mechanism revealed within the first 2 min of irradiation there was the formation of a diol species due to consumption of the alkene sidechain. Although the data presented highlights the complexity of the system, which is underpinned by multiple oxidative reaction pathways, an overview of the key photocatalytic processes are discussed including the impact of acetonitrile and role of reactive oxygen species.
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