Kumaravel Sangeetha, Thiruvengetam Prabaharan, Karthick Kannimuthu, Sankar Selvasundarasekar Sam, Karmakar Arun, Kundu Subrata
Electrochemical Process Engineering (EPE) Division, CSIR-Central Electrochemical Research Institute (CECRI), Karaikudi, 630003, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.
Biotechnol Prog. 2021 Mar;37(2):e3111. doi: 10.1002/btpr.3111. Epub 2020 Dec 30.
Depolymerization of lignin biomass to its value-added chemicals and fuels is pivotal for achieving the goals for sustainable society, and therefore has acquired key interest among the researchers worldwide. A number of distinct approaches have evolved in literature for the deconstruction of lignin framework to its mixture of complex constituents in recent decades. Among the existing practices, special attention has been devoted for robust site selective chemical transformation in the complex structural frameworks of lignin. Despite the initial challenges over a period of time, oxidation and oxidative cleavage process of aromatic building blocks of lignin biomass toward the fine chemical synthesis and fuel generation has improved substantially. The development has improved in terms of cost effectiveness, milder reaction conditions, and purity of compound individuals. These aforementioned oxidative protocols mainly involve the breaking of C-C and C-O bonds of complex lignin frameworks. More precisely in the line with environmentally friendly greener approach, the catalytic oxidation/oxidative cleavage reactions have received wide spread interest for their mild and selective nature toward the lignin depolymerization. This mini-review aims to provide an overview of recent developments in the field of oxidative depolymerization of lignin under greener and environmentally benign conditions. Also, these oxidation protocols have been discussed in terms of scalability and recyclability as catalysts for different fields of applications.
将木质素生物质解聚为增值化学品和燃料对于实现可持续社会目标至关重要,因此已引起全球研究人员的高度关注。近几十年来,文献中出现了许多不同的方法来将木质素框架解构为其复杂成分的混合物。在现有实践中,人们特别关注在木质素复杂结构框架中进行强大的位点选择性化学转化。尽管在一段时间内存在最初的挑战,但木质素生物质芳香结构单元向精细化学品合成和燃料生成的氧化及氧化裂解过程已得到显著改善。在成本效益、更温和的反应条件和化合物个体纯度方面都有了改进。上述氧化方法主要涉及复杂木质素框架中碳 - 碳键和碳 - 氧键的断裂。更确切地说,符合环境友好的绿色方法,催化氧化/氧化裂解反应因其对木质素解聚的温和性和选择性而受到广泛关注。本综述旨在概述在更绿色和环境友好条件下木质素氧化解聚领域的最新进展。此外,还讨论了这些氧化方法作为不同应用领域催化剂的可扩展性和可回收性。