4.7 Article

Highly efficient CO removal by active cuprous-based ternary deep eutectic solvents [HDEEA][Cl] plus CuCl plus EG

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ELSEVIER
DOI: 10.1016/j.seppur.2021.118985

关键词

Deep eutectic solvent; Cuprous; CO; Removal; Anion

资金

  1. Natural Science Foundation of China [22078294]
  2. Zhejiang Provincial Natural Science Foundation of China [LZ21E80001, LGF20E080018]

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A series of active cuprous-based ternary deep eutectic solvents were designed and prepared for capturing carbon monoxide in hydrogen gas, and the efficiency and mechanism of CO capture at different molar ratios were analyzed. The presence of Cu(I) was found to be crucial for efficient CO capture by these DESs, and Delta H was identified as the main driving force for CO capture.
Carbon monoxide (CO) is a kind of impurity gas in hydrogen (H2), resulting to catalyst poisoning in protonexchange-membrane fuel cells (PEMFCs). On the other hand, CO is harmful to human health due to its colorlessness, odorlessness and high toxicity. In this contribution, a series of active cuprous-based ternary deep eutectic solvents (DESs) with 2-diethylaminoethanol chloride ([HDEEA][Cl]) plus cuprous chloride (CuCl) plus ethylene glycol (EG) at different molar ratios (1:1:4, 1:1:2 and 1:1:1) were designed and prepared. Physical properties such as density and viscosity of these DESs were measured at different temperatures. CO capture by these DESs were investigated at different concentrations of CO and different temperatures. It was found that the capture capacities of 0.203 and 0.564 mol CO per mole DES could be reached by [HDEEA][Cl] + CuCl + EG with n[HDEEA][Cl]:nCuCl:nEG = 1:1:4 at 293.2 K and 1 bar or 5 bar, respectively. FT-IR method was used to investigate the mechanism of CO removal. These results suggested that the presence of Cu(I) is crucial for efficient capture of CO by these ternary DESs while - OH groups and EG could release the activity of Cu(I). Furthermore, the thermodynamic properties such as the Gibbs free energy change (Delta G), enthalpy change (Delta H), and entropy change (Delta S) for CO capture by [HDEEA][Cl] + CuCl + EG (1:1:4) were obtained, and Delta H was the main driving force for CO capture.

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