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Separation of n/iso-paraffins in a hierarchically structured 3D-printed porous carbon monolith

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Resumo:Hierarchically structured 3D-printed porous carbons monoliths were investigated for their applicability in adsorptive n/iso-paraffin separation. Three materials of the same macroscopic shape were employed, which varied in the micro- and mesoporosity by altering the final CO2 activation step: non-activated and activated at 1133 K for 6 and 12 h, respectively. Chromatographic breakthrough experiments were conducted for pentane and hexane isomer mixtures at industrially relevant separation conditions. Results demonstrated that the initial porosity for the non-activated monolith enables the complete separation of linear paraffins from their branched isomers (slightly adsorbed) via a near molecular sieving effect. The Langmuir isotherm conveniently fitted the adsorption equilibrium data, and a dynamic mathematical model suitably predicted the breakthrough curves. Regarding the CO2 activated monoliths, both showed adsorption towards all alkanes with practically no selectivity between them.
Autores principais:Henrique, Adriano
Outros Autores:Zafanelli, Lucas F.A.S.; Aly, Ezzeldin; Steldinger, Hendryk; Gläsel, Jan; Rodrigues, Alírio; Etzold, Bastian J.M.; Silva, José A.C.
Assunto:RON improvement of gasoline Pentane and hexane isomers separation by adsorption 3D-printed carbon monoliths
Ano:2023
País:Portugal
Tipo de documento:documento de conferência
Tipo de acesso:acesso aberto
Instituição associada:Instituto Politécnico de Bragança
Idioma:inglês
Origem:Biblioteca Digital do IPB
Descrição
Resumo:Hierarchically structured 3D-printed porous carbons monoliths were investigated for their applicability in adsorptive n/iso-paraffin separation. Three materials of the same macroscopic shape were employed, which varied in the micro- and mesoporosity by altering the final CO2 activation step: non-activated and activated at 1133 K for 6 and 12 h, respectively. Chromatographic breakthrough experiments were conducted for pentane and hexane isomer mixtures at industrially relevant separation conditions. Results demonstrated that the initial porosity for the non-activated monolith enables the complete separation of linear paraffins from their branched isomers (slightly adsorbed) via a near molecular sieving effect. The Langmuir isotherm conveniently fitted the adsorption equilibrium data, and a dynamic mathematical model suitably predicted the breakthrough curves. Regarding the CO2 activated monoliths, both showed adsorption towards all alkanes with practically no selectivity between them.