| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 74312 | Microporous and Mesoporous Materials | 2011 | 5 Pages |
Divalent cation-exchanged ETS-4 such as Ca2+, Sr2+, and Ba2+ was successfully prepared via ion exchange process. TPD analysis for CO2 shows two distinct peaks based on 187 °C. As the pretreatment temperature increased from 200 °C to 250 °C in TPD analysis, the amount of desorbed CO2 from high peak (i.e. oxygen basic site) was decreased while that from low peak (i.e. M2+-CO2 interaction) was a little increased. Unexpectedly, the amount of CO2 adsorbed on cation site for Ca-ETS-4 was the lowest despite that the electronegativity of Ca2+ is the largest. It is attributed to possible shielding of small cation by the first few molecules of a cavity. The decrease of % change in the amount of CO2 adsorbed on oxygen basic site with the increase in pretreatment temperature for Ca-ETS-4 was most significant arisen from weak basicity of oxygen basic site due to small electronegativity of Ca2+ compared to other two cations. In case of large cation, Ba-ETS-4, however, the increase of % change in the amount of CO2 adsorbed on cation site was most significant due to less shielding effect as well as higher degree of dehydration of Ba2+. The adsorption of CO2 using BET apparatus was well consistent with that of a single adsorption capacity using gravimetric method.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Adsorption characteristics of CO2 on divalent cation exchanged ETS-4 such as Ca2+, Sr2+, and Ba2+ was investigated. ► TPD analysis shows that the ion exchange of Na/K-ETS-4 by divalent cations has shifted desorption temperatures to higher temperature. ► The amount of desorbed CO2 from high peak was decreased while that from low peak was rather increased with pretreatment temperature. ► CO2 adsorption on cationic sites due to CO2-M interaction was increased, making the access of CO2 to framework basic O-site difficult.
