{"title":"Insight into CO2 capture by aqueous solutions of N,N-diethylethanolamine promoted with potassium salts of amino acids","authors":"Hitesh D. Rawate, Prakash D. Vaidya","doi":"10.1002/cjce.25309","DOIUrl":null,"url":null,"abstract":"<p>N,N-Diethylethanolamine (DEEA) is a potential high-capacity CO<sub>2</sub>-capturing solvent. The CO<sub>2</sub> reactivity of DEEA can be improved by the addition of rate promoters. Both equilibrium CO<sub>2</sub> solubility and desorption rate are also influenced by promoters. In this work, the effect of promotion of DEEA with three amino acid salts, potassium arginate (PA), potassium prolinate (PP), and potassium glycinate (PG), was investigated. In a stirred cell reactor, CO<sub>2</sub> reactivity of the promoted solutions was studied at 303 K. Rate promotion with PA was most effective; this was then followed by PP and PG. The value of the liquid-side mass transfer coefficient (0.005 cm/s) for CO<sub>2</sub> absorption in water inside the stirred cell was found. Equilibrium CO<sub>2</sub> solubility in the promoted mixtures was measured. Empirical equations that predicted solubility data (accuracy 99%) were proposed. Desorption trials were performed at 363 K. PA, PP, and PG lowered sensible energy constraint by 59%, 32%, and 30%. PA was most-suited for faster desorption of aqueous solutions of DEEA. Overall, potassium salts of arginine, proline, and glycine were promising candidates for improving the performance of the tertiary amine DEEA. Finally, catalytic desorption of loaded solutions of DEEA was studied and it was found that alumina was a promising catalyst for faster desorption.</p>","PeriodicalId":9400,"journal":{"name":"Canadian Journal of Chemical Engineering","volume":"102 12","pages":"4359-4370"},"PeriodicalIF":1.6000,"publicationDate":"2024-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Canadian Journal of Chemical Engineering","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cjce.25309","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
N,N-Diethylethanolamine (DEEA) is a potential high-capacity CO2-capturing solvent. The CO2 reactivity of DEEA can be improved by the addition of rate promoters. Both equilibrium CO2 solubility and desorption rate are also influenced by promoters. In this work, the effect of promotion of DEEA with three amino acid salts, potassium arginate (PA), potassium prolinate (PP), and potassium glycinate (PG), was investigated. In a stirred cell reactor, CO2 reactivity of the promoted solutions was studied at 303 K. Rate promotion with PA was most effective; this was then followed by PP and PG. The value of the liquid-side mass transfer coefficient (0.005 cm/s) for CO2 absorption in water inside the stirred cell was found. Equilibrium CO2 solubility in the promoted mixtures was measured. Empirical equations that predicted solubility data (accuracy 99%) were proposed. Desorption trials were performed at 363 K. PA, PP, and PG lowered sensible energy constraint by 59%, 32%, and 30%. PA was most-suited for faster desorption of aqueous solutions of DEEA. Overall, potassium salts of arginine, proline, and glycine were promising candidates for improving the performance of the tertiary amine DEEA. Finally, catalytic desorption of loaded solutions of DEEA was studied and it was found that alumina was a promising catalyst for faster desorption.
期刊介绍:
The Canadian Journal of Chemical Engineering (CJChE) publishes original research articles, new theoretical interpretation or experimental findings and critical reviews in the science or industrial practice of chemical and biochemical processes. Preference is given to papers having a clearly indicated scope and applicability in any of the following areas: Fluid mechanics, heat and mass transfer, multiphase flows, separations processes, thermodynamics, process systems engineering, reactors and reaction kinetics, catalysis, interfacial phenomena, electrochemical phenomena, bioengineering, minerals processing and natural products and environmental and energy engineering. Papers that merely describe or present a conventional or routine analysis of existing processes will not be considered.