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   <subfield code="a">Can alkane isomers be separated? Adsorption equilibrium and kinetic data for hexane isomers and their binary mixtures on MFI</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Alexandre Ferreira, Marjo Mittelmeijer-Hazeleger, Alfred Bliek]</subfield>
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   <subfield code="a">In this study we present a global overview of the adsorption behavior of hexane isomers on MFI. With an experimental approach that couples a manometric technique with Near Infrared (NIR) spectroscopy, which has been recently developed, we did address adsorption kinetic properties of n-hexane, 2-methylpentane, 2,2-dimethylbutane and 2,3-dimethylbutane, and their binary mixtures. The adsorption equilibrium properties of the binary mixtures were also assessed using the same technique. Whereas the adsorption isotherms and heats of adsorption for single components have been studied by a manometric technique coupled with a micro calorimeter. The differential heats of adsorption of n-hexane increase slightly with loading, on the other hand the heat of adsorption of branched hexanes exhibits a decrease with loading. The diffusion rates on MFI of n-hexane, 2-methylpentane and 2,3-dimethylbutane are in the same order of magnitude. However, the diffusion rate of 2,2-dimethylbutane is two orders of magnitude lower than rates of the other isomers. In the binary mixtures the components interact and the difference between the diffusion rates of the components decreases. The MFI zeolite presents equilibrium selectivity towards the less branched isomers. In conclusion, a separation process for linear/mono-branched alkanes + double-branched alkanes, has to be based on its equilibrium properties and not based on adsorption kinetics.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2007</subfield>
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   <subfield code="a">Zeolites</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Alkanes</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Isotherms</subfield>
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   <subfield code="a">Differential heat of adsorption</subfield>
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   <subfield code="a">D : diffusivity, m2⋅s−1</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">D c : uptake diffusivity, m2⋅s−1</subfield>
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   <subfield code="a">D / r 2 : diffusion time constant, s−1</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">K C : adsorption equilibrium constant in the channels, kPa−1</subfield>
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   <subfield code="a">K I : adsorption equilibrium constant in the intersections, kPa−1</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">K H : Henry's Law constant, mmol⋅g−1⋅kPa−1</subfield>
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   <subfield code="a">p : pressure (adsorbate concentration in the gas phase), Pa</subfield>
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   <subfield code="a">Q 0 : initial heat of adsorption, kJ⋅mol−1</subfield>
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   <subfield code="a">q : loading (adsorbate concentration in the particles), mmol⋅g−1</subfield>
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   <subfield code="a">q sat , C : saturation loading in the channels, mmol⋅g−1</subfield>
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   <subfield code="a">q sat , I : saturation loading in the intersections, mmol⋅g−1</subfield>
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   <subfield code="a">q t : adsorbed amount at time t, mmol⋅g−1</subfield>
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   <subfield code="a">q inf : adsorbed amount at equilibrium, mmol⋅g−1</subfield>
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   <subfield code="a">r : particle radius, m</subfield>
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   <subfield code="a">V s : the volume of the sample, cm3</subfield>
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   <subfield code="a">V g : the volume of apparatus, cm3</subfield>
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   <subfield code="a">α : K c V s /V g ,(−)</subfield>
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