Saiyuan Xu, Yujun Guo, Yibin Wu, Bin Chen, Yingjie Xu
{"title":"Physicochemical Properties and CO2 Absorption of the Mixed System of Sodium Phenoxide and [Emim]Cl–EG Deep Eutectic Solvents","authors":"Saiyuan Xu, Yujun Guo, Yibin Wu, Bin Chen, Yingjie Xu","doi":"10.1007/s10953-026-01606-z","DOIUrl":null,"url":null,"abstract":"<div><p>This study aims to develop and characterize a novel mixed system composed of sodium phenoxide (NaOPh) and a deep eutectic solvent (DES) formed from 1-ethyl-3-methylimidazole chloride ([Emim]Cl) and ethylene glycol (EG), in order to address the phase separation issue commonly encountered in aqueous phenoxide solutions during CO₂ absorption—caused by the generation of phenol. The physicochemical properties, CO<sub>2</sub> absorption performance and absorption mechanism of the NaOPh/DES mixed system were investigated. The results indicate that the density, viscosity, and CO<sub>2</sub> absorption capacity of the studied NaOPh/DES mixed systems increase with NaOPh content. The NaOPh1.0/DES system exhibits the best absorption performance of these systems, with a CO<sub>2</sub> absorption capacity of 2.10 mol‧kg<sup>−1</sup> at 313.15 K and 0.1 MPa. DFT calculations reveal that the Na<sup>+</sup> from NaOPh, the O–H group from EG, and the Cl<sup>−</sup> from [Emim] Cl can form a stable four-membered ring. This weakens the electrostatic interaction between Na<sup>+</sup> and [PhO]<sup>−</sup>, promoting the dissociation of the NaOPh and facilitating the chemical reaction between the “free” [PhO]⁻ and CO<sub>2</sub> to form carbonates. This mechanism is confirmed by FT-IR and <sup>13</sup>C NMR spectra. Using [Emim]Cl–EG DES as a solvent to dissolve NaOPh leverages the reactivity of [PhO]<sup>−</sup> with CO<sub>2</sub> for efficient absorption, while effectively avoiding phase separation. This expands the application of phenoxide-based systems in CO₂ capture.</p></div>","PeriodicalId":666,"journal":{"name":"Journal of Solution Chemistry","volume":"55 8","pages":"1801 - 1817"},"PeriodicalIF":1.3000,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solution Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10953-026-01606-z","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
This study aims to develop and characterize a novel mixed system composed of sodium phenoxide (NaOPh) and a deep eutectic solvent (DES) formed from 1-ethyl-3-methylimidazole chloride ([Emim]Cl) and ethylene glycol (EG), in order to address the phase separation issue commonly encountered in aqueous phenoxide solutions during CO₂ absorption—caused by the generation of phenol. The physicochemical properties, CO2 absorption performance and absorption mechanism of the NaOPh/DES mixed system were investigated. The results indicate that the density, viscosity, and CO2 absorption capacity of the studied NaOPh/DES mixed systems increase with NaOPh content. The NaOPh1.0/DES system exhibits the best absorption performance of these systems, with a CO2 absorption capacity of 2.10 mol‧kg−1 at 313.15 K and 0.1 MPa. DFT calculations reveal that the Na+ from NaOPh, the O–H group from EG, and the Cl− from [Emim] Cl can form a stable four-membered ring. This weakens the electrostatic interaction between Na+ and [PhO]−, promoting the dissociation of the NaOPh and facilitating the chemical reaction between the “free” [PhO]⁻ and CO2 to form carbonates. This mechanism is confirmed by FT-IR and 13C NMR spectra. Using [Emim]Cl–EG DES as a solvent to dissolve NaOPh leverages the reactivity of [PhO]− with CO2 for efficient absorption, while effectively avoiding phase separation. This expands the application of phenoxide-based systems in CO₂ capture.
期刊介绍:
Journal of Solution Chemistry offers a forum for research on the physical chemistry of liquid solutions in such fields as physical chemistry, chemical physics, molecular biology, statistical mechanics, biochemistry, and biophysics. The emphasis is on papers in which the solvent plays a dominant rather than incidental role. Featured topics include experimental investigations of the dielectric, spectroscopic, thermodynamic, transport, or relaxation properties of both electrolytes and nonelectrolytes in liquid solutions.