Loker Hydrocarbon Research Institute and Department of Chemistry, University of Southern California, University Park, Los Angeles, California 90089-1661, United States.
J Am Chem Soc. 2020 Mar 11;142(10):4544-4549. doi: 10.1021/jacs.9b12711. Epub 2020 Feb 12.
The first example of an alkali hydroxide-based system for CO capture and conversion to methanol has been established. Bicarbonate and formate salts were hydrogenated to methanol with high yields in a solution of ethylene glycol. In an integrated one-pot system, CO was efficiently captured by an ethylene glycol solution of the base and subsequently hydrogenated to CHOH at relatively mild temperatures (100-140 °C) using Ru-PNP catalysts. The produced methanol can be easily separated by distillation. Hydroxide base regeneration at low temperatures was observed for the first time. Finally, CO capture from ambient air and hydrogenation to CHOH was demonstrated. We postulate that the high capture efficiency and stability of hydroxide bases make them superior to existing amine-based routes for direct air capture and conversion to methanol in a scalable process.
首次建立了基于碱氢氧化物的 CO 捕获和转化为甲醇的体系。碳酸氢盐和甲酸盐在乙二醇溶液中以高收率氢化生成甲醇。在一个集成的一锅系统中,CO 被碱的乙二醇溶液有效捕获,然后在相对温和的温度(100-140°C)下使用 Ru-PNP 催化剂氢化生成 CHOH。生成的甲醇可以通过蒸馏轻松分离。首次观察到在低温下再生氢氧化物碱。最后,实现了从环境空气中捕获 CO 并将其氢化生成 CHOH。我们假设,与现有的基于胺的方法相比,氢氧化物碱具有更高的捕获效率和稳定性,使其成为一种可扩展的过程,用于直接从空气中捕获 CO 并转化为甲醇。