共 44 条
Tailored carbon dioxide capacity in carboxylate-based ionic liquids
被引:2
作者:

Scaglione, Nicolas
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机构:
Univ Lyon, Lab Chim ENS Lyon, CNRS, 46 Allee Italie, F-69364 Lyon, France Univ Lyon, Lab Chim ENS Lyon, CNRS, 46 Allee Italie, F-69364 Lyon, France

Avila, Jocasta
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Univ Lyon, Lab Chim ENS Lyon, CNRS, 46 Allee Italie, F-69364 Lyon, France Univ Lyon, Lab Chim ENS Lyon, CNRS, 46 Allee Italie, F-69364 Lyon, France

Padua, Agilio
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机构:
Univ Lyon, Lab Chim ENS Lyon, CNRS, 46 Allee Italie, F-69364 Lyon, France Univ Lyon, Lab Chim ENS Lyon, CNRS, 46 Allee Italie, F-69364 Lyon, France

Gomes, Margarida Costa
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机构:
Univ Lyon, Lab Chim ENS Lyon, CNRS, 46 Allee Italie, F-69364 Lyon, France Univ Lyon, Lab Chim ENS Lyon, CNRS, 46 Allee Italie, F-69364 Lyon, France
机构:
[1] Univ Lyon, Lab Chim ENS Lyon, CNRS, 46 Allee Italie, F-69364 Lyon, France
关键词:
CO2;
ABSORPTION;
ANION;
CAPTURE;
CHEMISORPTION;
DISSOLUTION;
SOLUBILITY;
D O I:
10.1039/d4fd00052h
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
We have used a library of thermally stable tetraalkylphosphonium carboxylate ionic liquids that were easily prepared from available carboxylic acids. Depending on the pKa in water of the precursor acids, the resulting ionic liquids either dissolve or reversibly chemically absorb CO2, with some exhibiting notable gas capacities, reaching a CO2 mole fraction of 0.2 at 1 bar and 343 K. While equilibrium constants and ionic liquid capacities generally correlate with the pKa of the acids, certain exceptions underscore the influence of liquid structure and physical properties of the ionic liquids, elucidated through molecular dynamics simulations and density functional theory calculations. Unlike the trends observed in other CO2-absorbing ILs, phosphonium carboxylates do not experience increased viscosity upon gas absorption; instead, enhanced diffusivities are observed, facilitating efficient gas-liquid transfer. Tetraalkylphosphonium carboxylate ionic liquids absorb large quantities of carbon dioxide and are easily regenerated.
引用
收藏
页码:233 / 250
页数:18
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