Publication
CO2 Capture in Chemically and Thermally Modified Activated Carbons Using Breakthrough Measurements: Experimental and Modeling Study
| dc.contributor.author | Silva, José A.C. | |
| dc.contributor.author | Karimi, Mohsen | |
| dc.contributor.author | Gonçalves, Carmem Natália de Pina | |
| dc.contributor.author | Díaz de Tuesta, Jose Luis | |
| dc.contributor.author | Rodrigues, Alírio | |
| dc.contributor.author | Gomes, Helder | |
| dc.date.accessioned | 2018-02-19T10:00:00Z | |
| dc.date.accessioned | 2019-02-04T17:10:35Z | |
| dc.date.available | 2018-01-19T10:00:00Z | |
| dc.date.available | 2019-02-04T17:10:35Z | |
| dc.date.issued | 2018 | |
| dc.description.abstract | The development of adsorption-based technologies for CO2 capture in the post combustion processes requires finding materials with high capacity of adsorption and low cost of preparation. In this study, the modification of a commercial activated carbon (Norit ROX 0.8), considered as a solid adsorbent for CO2 capture, and the effects of different methods of activations, chemically (hydrogen peroxide, sulfuric acid, nitric acid, and urea) and thermally (at 800 °C) on adsorption performance, have been investigated. Then, CO2 adsorption capacity was studied at different temperatures and pressures to evaluate the effects of various agents on sample performance. The textural properties of the samples were determined using adsorption−desorption isotherms of nitrogen at −196 °C. Finally, the obtained data were modeled by Response Surface Methodology (RSM) and Langmuir isotherm. The results showed that the prepared sample by successive treatments with nitric acid, urea, and thermal calcination has a higher uptake capacity than other modified samples. | en_EN |
| dc.description.sponsorship | This work was financially supported by Project POCI-01-0145- FEDER-006984 − Associate Laboratory LSRE-LCM funded by FEDER through COMPETE2020 - Programa Operacional Competitividade e Internacionalização (POCI) − and by national funds through FCT - Fundação para a Ciência e a Tecnologia. M.K. also acknowledges a research grant awarded under project ″VALORCOMP″ (ref.0119_VALORCOMP_ 2_P), financed through INTERREG V A Spain Portugal (POCTEP) 2014-2020, under the European Regional Development Fund by FCT. | |
| dc.description.version | info:eu-repo/semantics/publishedVersion | en_EN |
| dc.identifier.citation | Karimi, Mohsen; Silva, José A.C.; Gonçalves, Carmem Natália; Diaz de Tuesta, José L.; Rodrigues, Alírio E.; Gomes, Helder T. (2018). CO2 Capture in Chemically and Thermally Modified Activated Carbons Using Breakthrough Measurements: Experimental and Modeling Study. Industrial and Engineering Chemistry Research. ISSN 0888-5885. 57, p. 11154-11166 | en_EN |
| dc.identifier.doi | 10.1021/acs.iecr.8b00953 | en_EN |
| dc.identifier.issn | 0888-5885 | |
| dc.identifier.uri | http://hdl.handle.net/10198/18733 | |
| dc.language.iso | eng | |
| dc.peerreviewed | yes | en_EN |
| dc.subject | Activated carbon | |
| dc.subject | Adsorption isotherms | |
| dc.subject | Carbon dioxide | |
| dc.subject | Mesoporous materials | |
| dc.title | CO2 Capture in Chemically and Thermally Modified Activated Carbons Using Breakthrough Measurements: Experimental and Modeling Study | en_EN |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| person.familyName | Silva | |
| person.familyName | Díaz de Tuesta | |
| person.familyName | Gomes | |
| person.givenName | José A.C. | |
| person.givenName | Jose Luis | |
| person.givenName | Helder | |
| person.identifier.ciencia-id | C11B-F5CF-7C78 | |
| person.identifier.ciencia-id | 7A1F-022B-7DBF | |
| person.identifier.ciencia-id | 6218-1E19-13EE | |
| person.identifier.orcid | 0000-0003-1778-3833 | |
| person.identifier.orcid | 0000-0003-2408-087X | |
| person.identifier.orcid | 0000-0001-6898-2408 | |
| person.identifier.rid | D-9785-2017 | |
| person.identifier.scopus-author-id | 7403023684 | |
| person.identifier.scopus-author-id | 55755821600 | |
| rcaap.rights | openAccess | en_EN |
| rcaap.type | article | en_EN |
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