The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Recent advances in capture of carbon dioxide using alkali-metal-based oxides
Abstract
Carbon dioxide (CO2) is a major greenhouse gas and makes a significant contribution to global warming and climate change. Thus CO2 capture and storage (CCS) have attracted worldwide interest from both fundamental and practical research communities. Alkali-metal-based oxides such as alkali-metal oxides, binary oxides, and hydrotalcite-like compounds are promising adsorbents for CO2 capture because of their relatively high adsorption capacity, low cost, and wide availability. They can also be applied to the adsorption-enhanced reactions involving CO2. The microstructures (e.g., surface area, porosity, particle size, and dispersion) of these oxides determine the CO2 adsorption capacity and multicycle stability. This perspective critically assesses and gives an overview of recent developments in the synthesized method, adsorption mechanism, operational conditions, stability, and regenerability of a variety of oxides. Both pros and cons of these oxides are also discussed. Insights are provided into several effective procedures regarding microstructural control of alkali-metal-based oxides, including preparation optimization, modification, stream hydration, etc.
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Citations
Cites
Recent advances in catalytic hydrogenation of carbon dioxide
Wang, W., Wang, S., Ma, X., & Gong, J. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15008a · Cited by 3,316
Self-citationAn overview of CO2 capture technologies
MacDowell, N., Florin, N., Buchard, A., Hallett, J., Galindo, A., Jackson, G., Adjiman, C. S., Williams, C. K., Shah, N., & Fennell, P. (2010) · Energy & Environmental Science · doi:10.1039/c004106h · Cited by 1,636
CO2 capture by solid adsorbents and their applications: current status and new trends
Wang, Q., Luo, J., Zhong, Z., & Borgna, A. (2011) · Energy Environ. Sci. · doi:10.1039/c0ee00064g · Cited by 1,611
Sorbents for CO2 capture from flue gas—aspects from materials and theoretical chemistry
Hedin, N., Chen, L., & Laaksonen, A. (2010) · Nanoscale · doi:10.1039/c0nr00042f · Cited by 243
CO2 Sorption on MgO and CaO Surfaces: A Comparative Quantum Chemical Cluster Study
Jensen, M. B., Pettersson, L. G. M., Swang, O., & Olsbye, U. (2005) · The Journal of Physical Chemistry B · doi:10.1021/jp052037h · Cited by 169
Cited by
Industrial carbon dioxide capture and utilization: state of the art and future challenges
Gao, W., Liang, S., Wang, R., Jiang, Q., Zhang, Y., Zheng, Q., Xie, B., Toe, C. Y., Zhu, X., Wang, J., et al. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00025f · Cited by 1,388
Graphene-based materials: Synthesis and gas sorption, storage and separation
Gadipelli, S., & Guo, Z. X. (2015) · Progress in Materials Science · doi:10.1016/j.pmatsci.2014.10.004 · Cited by 734
Porous materials for carbon dioxide separations
Siegelman, R. L., Kim, E. J., & Long, J. R. (2021) · Nature Materials · doi:10.1038/s41563-021-01054-8 · Cited by 722
Sharma, R. K., Yadav, P., Yadav, M., Gupta, R., Rana, P., Srivastava, A., Zbořil, R., Varma, R. S., Antonietti, M., & Gawande, M. B. (2020) · Materials Horizons · doi:10.1039/c9mh00856j · Cited by 455
Muraza, O., & Galadima, A. (2015) · International Journal of Energy Research · doi:10.1002/er.3295 · Cited by 381
Metadata
- Authors
- Wang, S., Yan, S., Ma, X., & Gong, J.
- Venue
- Energy & Environmental Science
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2011
- Volume
- 4
- Issue
- 10
- Pages
- 3805
- ISSN
- 1754-5692 (ISSN-L)
- 1754-5706
- OpenAlex
- W2093327861
- Cited by
- 382
- References
- 5
- FWCI
- 37.56
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
