Akashige Toshihiro, Vemuri Ramraj, Blanco César A Urbina, Modestino Miguel A
Department of Chemical and Biomolecular Engineering, New York University, Brooklyn, NY, 11201, USA.
Laboratory for Chemical Technology (LCT), Department of Materials, Textiles and Chemical Engineering. University of Ghent, Ghent, 9052, Belgium.
React Chem Eng. 2024 Aug 1;9(8):2171-2179. doi: 10.1039/d4re00145a. Epub 2024 May 13.
Olefin-paraffin separation is a critical yet energy-intensive process in the chemical industry, accounting for over 250 trillion BTU/year of global energy consumption. This work explores the use of redox-active nickel maleonitriledithiolate complex for olefin-paraffin separations. Key performance factors, namely the electrochemical oxidation of the complex and the olefin capture utilization fraction, were systematically quantified. Electrochemical studies revealed near-complete oxidation of Ni(II) to Ni(IV) species, suggesting that the electrochemical oxidation step is not a limiting factor in olefin capture. The utilization fraction was found to be strongly dependent on the complexation equilibrium behavior between olefin-bound and unbound state of the complex. Time-resolved kinetic measurements unveiled a sluggish complexation rate, requiring over 36 hours to approach equilibrium. These insights highlight the importance of driving the complexation equilibrium and improving the kinetics to enhance the performance of Ni-based electrochemical swing absorbers for energy-efficient olefin-paraffin separations. The findings lay the groundwork for future optimization strategies and industrial implementation of this sustainable separation technology.
烯烃 - 石蜡分离是化学工业中一个关键但能源密集型的过程,占全球能源消耗每年超过250万亿英热单位。这项工作探索了氧化还原活性马来腈二硫醇镍配合物在烯烃 - 石蜡分离中的应用。系统地量化了关键性能因素,即配合物的电化学氧化和烯烃捕获利用率。电化学研究表明Ni(II)几乎完全氧化为Ni(IV)物种,这表明电化学氧化步骤不是烯烃捕获的限制因素。发现利用率强烈依赖于配合物的烯烃结合态和未结合态之间的络合平衡行为。时间分辨动力学测量揭示了缓慢的络合速率,需要超过36小时才能达到平衡。这些见解突出了驱动络合平衡和改善动力学对于提高基于镍的电化学变压吸收器用于节能烯烃 - 石蜡分离性能的重要性。这些发现为这种可持续分离技术的未来优化策略和工业应用奠定了基础。