1997
DOI: 10.1006/jcis.1997.5099
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Determining Surface Areas from Linear Adsorption Isotherms at Supercritical Conditions

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Cited by 39 publications
(24 citation statements)
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“…The necessary variable that remains unknown is the volume of the adsorption layer and numerous methods have been suggested to estimate it. Typical methods include fixing the volume of adsorption as the total pore volume of the sorbent material, 1 using a volume proportional to the surface area (assuming fixed thickness), 20 or deriving the volume by assuming the adsorbed layer is at liquid density. 21 Some approaches are specific to graphite-like carbon materials, such as the Ono-Kondo model.…”
Section: Thermodynamic Analysis Of Adsorption Isotherm Datamentioning
confidence: 99%
“…The necessary variable that remains unknown is the volume of the adsorption layer and numerous methods have been suggested to estimate it. Typical methods include fixing the volume of adsorption as the total pore volume of the sorbent material, 1 using a volume proportional to the surface area (assuming fixed thickness), 20 or deriving the volume by assuming the adsorbed layer is at liquid density. 21 Some approaches are specific to graphite-like carbon materials, such as the Ono-Kondo model.…”
Section: Thermodynamic Analysis Of Adsorption Isotherm Datamentioning
confidence: 99%
“…Similar approaches based on high-pressure adsorption data have been used pre-Ž . viously to estimate adsorbed phase properties Menon, 1968 Ž as well as adsorbent surface area Aranovich and Donohue, . 1997a .…”
Section: Total Adsorption From Gibbsian Excessmentioning
confidence: 99%
“…This phenomenon is the basis of a method to determine the specific surface area of the adsorbent, independent of the space requirements of the adsorbate molecule [16]. This method is also applicable to zeolites such as Na-Y [17].…”
Section: Adsorptionmentioning
confidence: 99%
“…In single-component adsorption at supercritical conditions, the adsorbed phase approaches a constant volume and a constant density with increasing pressures [16,17]. This phenomenon is the basis of a method to determine the specific surface area of the adsorbent, independent of the space requirements of the adsorbate molecule [16].…”
Section: Adsorptionmentioning
confidence: 99%