Khachatryan Lavrent, Barekati-Goudarzi Mohamad, Asatryan Rubik, Ozarowski Andrew, Boldor Dorin, Lomnicki Slawomir M, Cormier Stephania A
Department of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70803, United States.
Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Buffalo, New York 14260, United States.
ACS Omega. 2022 Aug 16;7(34):30241-30249. doi: 10.1021/acsomega.2c03381. eCollection 2022 Aug 30.
To assess contribution of the radicals formed from biomass burning, our recent findings toward the formation of resonantly stabilized persistent radicals from hydrolytic lignin pyrolysis in a metal-free environment are presented in detail. Such radicals have particularly been identified during fast pyrolysis of lignin dispersed into the gas phase in a flow reactor. The trapped radicals were analyzed by X-band electron paramagnetic resonance (EPR) and high-frequency (HF) EPR spectroscopy. To conceptualize available data, the metal-free biogenic bulky stable radicals with extended conjugated backbones are suggested to categorize as a new type of metal-free environmentally persistent free radicals (EPFRs) (bio-EPFRs). They can be originated not only from lignin/biomass pyrolysis but also during various thermal processes in combustion reactors and media, including tobacco smoke, anthropogenic sources and wildfires (forest/bushfires), and so on. The persistency of bio-EPFRs from lignin gas-phase pyrolysis was outlined with the evaluated lifetime of two groups of radicals being 33 and 143 h, respectively. The experimental results from pyrolysis of coniferyl alcohol as a model compound of lignin in the same fast flow reactor, along with our detailed potential energy surface analyses using high-level DFT and ab initio methods toward decomposition of a few other model compounds reported earlier, provide a mechanistic view on the formation of C- and O-centered radicals during lignin pyrolysis. The preliminary measurements using HF-EPR spectroscopy also support the existence of O-centered radicals in the radical mixtures from pyrolysis of lignin possessing a high value (2.0048).
为了评估生物质燃烧产生的自由基的贡献,我们详细介绍了近期在无金属环境下水解木质素热解形成共振稳定持久性自由基的研究结果。在流动反应器中木质素分散到气相的快速热解过程中特别鉴定出了这类自由基。通过X波段电子顺磁共振(EPR)和高频(HF)EPR光谱对捕获的自由基进行了分析。为了梳理现有数据,建议将具有扩展共轭骨架的无金属生物源大体积稳定自由基归类为一种新型的无金属环境持久性自由基(EPFRs)(生物-EPFRs)。它们不仅可以源自木质素/生物质热解,还可以在燃烧反应器和介质中的各种热过程中产生,包括烟草烟雾、人为来源和野火(森林/丛林火灾)等。木质素气相热解产生的生物-EPFRs的持久性通过评估两组自由基的寿命分别为33小时和143小时来概述。在同一快速流动反应器中,以松柏醇作为木质素的模型化合物进行热解的实验结果,以及我们使用高水平密度泛函理论(DFT)和从头算方法对之前报道的其他几种模型化合物分解进行的详细势能面分析,提供了木质素热解过程中碳中心和氧中心自由基形成的机理观点。使用HF-EPR光谱的初步测量也支持在具有高 值(2.0048)的木质素热解产生的自由基混合物中存在氧中心自由基。