Please use this identifier to cite or link to this item: https://doi.org/10.1021/la049947v
DC FieldValue
dc.titleCO2 adsorption over Si-MCM-41 materials having basic sites created by postmodification with La2O3
dc.contributor.authorShen, S.C.
dc.contributor.authorChen, X.
dc.contributor.authorKawi, S.
dc.date.accessioned2014-10-09T06:44:49Z
dc.date.available2014-10-09T06:44:49Z
dc.date.issued2004-10-12
dc.identifier.citationShen, S.C., Chen, X., Kawi, S. (2004-10-12). CO2 adsorption over Si-MCM-41 materials having basic sites created by postmodification with La2O3. Langmuir 20 (21) : 9130-9137. ScholarBank@NUS Repository. https://doi.org/10.1021/la049947v
dc.identifier.issn07437463
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/88656
dc.description.abstractModerate basic sites could be created onto mesoporous Si-MCM-41 materials by postsynthesis modification with highly dispersed La2O 3. The La2O3-modified MCM-41 materials (designated here as LaM) have been characterized by Fourier transform infrared spectroscopy, temperature-programmed desorption, X-ray photoelectron spectroscopy, X-ray diffraction (XRD), and N2 adsorption/desorption and have been tested as model adsorbents for CO2 adsorption. XRD and N2 adsorption results showed that all LaM materials still maintained their uniform hexagonal mesoporous structure even after postsynthesis modification with La2O3 loading up to 20 wt %. Although the surface area, pore size, and pore volume of LaM materials decreased with increasing La2O3 loading, their capacity for CO 2 storage could be significantly improved when La2O 3 loading was increased from 0 to 10 wt %. Unidentate and bidentate carbonates have been identified by in situ FTIR as the two types of CO 2 species adsorbed on LaM surface. The LaM material also possesses good thermal stability, allowing the model adsorbent to be regenerated at high temperature and recyclable.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/la049947v
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/la049947v
dc.description.sourcetitleLangmuir
dc.description.volume20
dc.description.issue21
dc.description.page9130-9137
dc.description.codenLANGD
dc.identifier.isiut000224391600029
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