Utilize este identificador para referenciar este registo: http://hdl.handle.net/10198/3311
Título: Single- and multicomponent vapor-phase adsorption of xylene isomers and ethylbenzene in a microporous metal-organic famework
Autor: Nicolau, Marco
Bárcia, Patrick da Silva
Gallegos, José
Silva, José A.C.
Rodrigues, A.E.
Chen, Banglin
Palavras-chave: Adsorption
Data: 2009
Editora: ACS
Citação: Nicolau, Marco; Barcia, Patrick; Gallegos, Jose; Silva, Jose A. C.; Rodrigues, Alirio; Chen, Banglin (2009). Single- and multicomponent vapor-phase adsorption of xylene isomers and ethylbenzene in a microporous metal-organic famework. Journal of Physical Chemistry C. ISSN 1932-7447. 113:30, p. 13173-13179
Resumo: Vapor-phase adsorption of the C8 alkylaromatic components p-xylene (p-x), m-xylene (m-x), o-xylene (o-x), and ethylbenzene (eb) on the three-dimensional rnicroporous metal-organic framework (MOF) Zn(BDC)-(Dabco)(0.5) (BDC = 1,4-benzenedicarboxylate, Dabco = 1,4-diazabicyclo[2.2.2]octane) was investigated. Single- and multicomponent fixed-bed experiments were carried out at temperatures ranging from 125 to 175 degrees C and total hydrocarbon pressures up to 0.10 bar. At high pressure, the adsorption capacity for all the components varies from 35 to 26 g/100 g(ads) at 125 and 175 degrees C. Henry's constants are slightly different for all C8 alkylaromatics, except for o-xylene, which is significantly higher. The adsorption enthalpies at zero coverage for the different isomers ranges from 77.40 (eb) to 79.84 kJ/mol (o-x), indicating that the C8 alkylaromatics have comparable interactions with the framework at the low coverage, On the basis of binary and quaternary breakthrough experiments performed at different hydrocarbon pressures and temperatures, MOF Zn(BDC)(Dabco)(0.5) was realized for the efficient and feasible separation of o-xylene from other C8 alkylaromatic components with the selectivity up to 1.88 because of the stronger interactions between o-xylene molecules and the framework and their differential pore-filling and molecular-packing effects confined within nanopores of MOFs.
Peer review: yes
URI: http://hdl.handle.net/10198/3311
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