Department of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois, United States.
J Phys Chem A. 2012 Jul 5;116(26):7098-106. doi: 10.1021/jp300405x. Epub 2012 Jun 22.
For over 90 years, researchers have postulated mechanisms for the cleavage of cellulose's glycosidic bonds and resulting formation of levoglucosan without reaching consensus. These reactions are key primary reactions in thermal processes for the production of carbon-neutral, renewable transportation fuels. Previous literature reports have proposed a variety of mainly heterolytic and homolytic mechanisms, but there has been insufficient evidence to settle the debate. Using density functional theory (DFT) methods and implicit solvent, we compared the likelihood of forming either radical or ionic intermediates. We discovered a concerted reaction mechanism that is more favorable than previously proposed mechanisms and is in better alignment with experimental findings. This new understanding of the mechanism of cellulose thermal decomposition opens the door to accurate process modeling and educated catalyst design, which are vital steps toward producing more cost-efficient renewable energy.
90 多年来,研究人员提出了纤维素糖苷键断裂的机制,并由此形成左旋葡聚糖,但尚未达成共识。这些反应是生产碳中性可再生运输燃料的热过程中的关键初级反应。先前的文献报道提出了多种主要的异裂和均裂机制,但没有足够的证据来解决这一争论。我们使用密度泛函理论(DFT)方法和隐溶剂,比较了形成自由基或离子中间体的可能性。我们发现了一种协同反应机制,比以前提出的机制更有利,并且更符合实验结果。这种对纤维素热分解机制的新认识为准确的过程建模和有针对性的催化剂设计开辟了道路,这是生产更具成本效益的可再生能源的关键步骤。