Toshihiro Akashige, Ramraj Vemuri, César A. Urbina Blanco and Miguel A. Modestino
{"title":"Understanding electrochemically induced olefin complexation: towards electrochemical olefin–paraffin separations†","authors":"Toshihiro Akashige, Ramraj Vemuri, César A. Urbina Blanco and Miguel A. Modestino","doi":"10.1039/D4RE00145A","DOIUrl":null,"url":null,"abstract":"<p >Olefin–paraffin separation is a critical yet energy-intensive process in the chemical industry, accounting for over 250 trillion BTU per year of global energy consumption. This work explores the use of a redox-active nickel maleonitriledithiolate complex for olefin–paraffin separations. Key performance factors, namely the electrochemical oxidation of the complex and olefin capture utilization fraction, were systematically quantified. Electrochemical studies revealed near-complete oxidation of Ni(<small>II</small>) to Ni(<small>IV</small>) 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 states 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.</p>","PeriodicalId":101,"journal":{"name":"Reaction Chemistry & Engineering","volume":" 8","pages":" 2171-2179"},"PeriodicalIF":3.4000,"publicationDate":"2024-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Chemistry & Engineering","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/re/d4re00145a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Olefin–paraffin separation is a critical yet energy-intensive process in the chemical industry, accounting for over 250 trillion BTU per year of global energy consumption. This work explores the use of a redox-active nickel maleonitriledithiolate complex for olefin–paraffin separations. Key performance factors, namely the electrochemical oxidation of the complex and 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 states 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.
期刊介绍:
Reaction Chemistry & Engineering is a new journal reporting cutting edge research into all aspects of making molecules for the benefit of fundamental research, applied processes and wider society.
From fundamental, molecular-level chemistry to large scale chemical production, Reaction Chemistry & Engineering brings together communities of chemists and chemical engineers working to ensure the crucial role of reaction chemistry in today’s world.