Characterisation of porous materials for bioseparation

被引:28
作者
Barrande, M. [1 ,2 ,3 ]
Beurroies, I. [1 ,2 ,3 ]
Denoyel, R. [1 ,2 ,3 ]
Tatarova, I. [4 ]
Gramblicka, M. [4 ]
Polakovic, M. [4 ]
Joehnck, M. [5 ]
Schulte, M. [5 ]
机构
[1] Univ Aix Marseille 1, Equipe Matdiv, Lab Chim Provence, CNRS,Ctr St Jerome,UMR 6264, F-13397 Marseille 20, France
[2] Univ Aix Marseille 2, Equipe Matdiv, Lab Chim Provence, CNRS,Ctr St Jerome,UMR 6264, F-13397 Marseille 20, France
[3] Univ Aix Marseille 3, Equipe Matdiv, Lab Chim Provence, CNRS,Ctr St Jerome,UMR 6264, F-13397 Marseille 20, France
[4] Slovak Univ Technol Bratislava, Dept Chem & Biochem Engn, Inst Chem & Environm Engn, Fac Chem & Food Technol, SK-81237 Bratislava, Slovakia
[5] Merck KGaA, Performance & Life Sci Chem R&D, D-64293 Darmstadt, Germany
关键词
Size-exclusion; Mercury porosimetry; Gas adsorption; Thermoporometry; Vapour desorption; PORE-SIZE DISTRIBUTIONS; CHROMATOGRAPHIC ADSORBENTS; CAPILLARY CONDENSATION; MESOPOROUS MATERIALS; MERCURY POROSIMETRY; NITROGEN SORPTION; CONNECTIVITY; GELS; THERMOPOROMETRY; EQUILIBRIUM;
D O I
10.1016/j.chroma.2009.07.075
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
A set of chromatographic materials for bioseparation were characterised by various methods. Both commercial materials and new supports presenting various levels of rigidity were analysed. The methods included size-exclusion and capillary phenomena based techniques. Both batch exclusion and inverse size-exclusion chromatography were used. Gas adsorption, mercury porosimetry and thermoporometry were applied as well as a new method based on water desorption starting from the saturated state. When the rigidity of adsorbents is high enough, the agreement is reasonable between the values of the structural parameters that were determined (surface area, porosity, and pore size) by various methods. Nevertheless, a part of macroporosity may not be evidenced by inverse size-exclusion chromatography whereas it is visible by batch exclusion and the other methods. When the rigidity decreases, for example with soft swelling gels, where standard nitrogen adsorption or mercury porosimetry are no more reliable, two main situations are encountered: either the methods based on capillary phenomena (thermoporometry or water desorption) overestimate the pore size with an amplitude that depends on the method, or in some cases it is possible to distinguish water involved in the swelling of pore walls from that involved in pore filling by capillary condensation. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:6906 / 6916
页数:11
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