Periodic Mesoporous Organosilicas as Adsorbents of Toxic Trace Gases out of the Ambient Air

New periodic mesoporous organosilicas were synthesized using [bis(triethoxysilyl)vinyl]aniline (BTEVA) and [bis(triethoxysilyl)vinyl]benzene (BTEVB) as precursors and by functionalizing the BTEVA PMO with aminopropyl groups. All PMO materials showed a high degree of hexagonal order in the respective...

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Veröffentlicht in:Zeitschrift für anorganische und allgemeine Chemie (1950) 2014-03, Vol.640 (3-4), p.632-640
Hauptverfasser: Martens, Sven, Ortmann, Roman, Brieler, Felix J., Pasel, Christoph, Joo Lee, Young, Bathen, Dieter, Fröba, Michael
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container_end_page 640
container_issue 3-4
container_start_page 632
container_title Zeitschrift für anorganische und allgemeine Chemie (1950)
container_volume 640
creator Martens, Sven
Ortmann, Roman
Brieler, Felix J.
Pasel, Christoph
Joo Lee, Young
Bathen, Dieter
Fröba, Michael
description New periodic mesoporous organosilicas were synthesized using [bis(triethoxysilyl)vinyl]aniline (BTEVA) and [bis(triethoxysilyl)vinyl]benzene (BTEVB) as precursors and by functionalizing the BTEVA PMO with aminopropyl groups. All PMO materials showed a high degree of hexagonal order in the respective P‐XRDs as well as high surface areas with narrow pore size distributions. The PMOs together with activated carbon were investigated with regards to their hexanal adsorption capacity in a gravimetric apparatus with an attached GC‐MS. For the amine PMOs two different regions during adsorption were found. In the first region loadings in the range of 30 wt% were reached by a fast adsorption process. In the second region the loading reached 50 wt% but with slower kinetics. In desorption experiments up to 150 °C the loading decreased from 50 wt% to 30 wt%, where an equilibrium state was observed. With GC‐MS and NMR the first region could be assigned to a chemisorption process, where the hexanal forms an imine group with the amine function in a Schiff base reaction. The subsequent second region can be assigned to weaker and thus reversible physisorption. The total capacity (first and second region) is substantially higher for the amine PMOs than for the activated carbon. Due to the chemical bonding in the chemisorption process, the desorption behavior is completely different: compared to the activated carbon the bonding of hexanal is much stronger for the amine PMOs.
doi_str_mv 10.1002/zaac.201300519
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Chem</addtitle><date>2014-03</date><risdate>2014</risdate><volume>640</volume><issue>3-4</issue><spage>632</spage><epage>640</epage><pages>632-640</pages><issn>0044-2313</issn><eissn>1521-3749</eissn><abstract>New periodic mesoporous organosilicas were synthesized using [bis(triethoxysilyl)vinyl]aniline (BTEVA) and [bis(triethoxysilyl)vinyl]benzene (BTEVB) as precursors and by functionalizing the BTEVA PMO with aminopropyl groups. All PMO materials showed a high degree of hexagonal order in the respective P‐XRDs as well as high surface areas with narrow pore size distributions. The PMOs together with activated carbon were investigated with regards to their hexanal adsorption capacity in a gravimetric apparatus with an attached GC‐MS. For the amine PMOs two different regions during adsorption were found. In the first region loadings in the range of 30 wt% were reached by a fast adsorption process. In the second region the loading reached 50 wt% but with slower kinetics. 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source Wiley Online Library Journals Frontfile Complete
subjects Adsorption
Aniline
Chemisorption
Imine
PMO
title Periodic Mesoporous Organosilicas as Adsorbents of Toxic Trace Gases out of the Ambient Air
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