Adsorptive crystallization of benzoic acid in aerogels from supercritical solutions

被引:38
作者
Gorle, B. S. K. [2 ]
Smirnova, I. [1 ]
Arlt, W. [2 ]
机构
[1] Tech Univ Hamburg, D-21073 Hamburg, Germany
[2] Univ Erlangen Nurnberg, D-91058 Erlangen, Germany
关键词
Aerogels; Supercritical carbon dioxide; Benzoic acid; Adsorptive crystallization; SILICA AEROGELS; CARBON-DIOXIDE; EQUILIBRIUM; SOLIDIFICATION; SOLUBILITY; STABILITY; SOLIDS;
D O I
10.1016/j.supflu.2010.01.006
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, adsorption and crystallization of benzoic acid in different porous carriers (silica aerogel, MCM41, Trisopor glass, zeolite) from supercritical CO2 solutions is studied. The main purpose is to reveal the influence of the adsorptive properties of the carrier on the crystallization behavior of the solute. Therefore, both adsorption and crystallization processes are studied as a function of carrier's surface properties. Adsorption of the solute and CO2 is measured in situ using a magnetic suspension balance, whereas crystallization is realized in a high pressure view cell. The carriers could be loaded with up to similar to 35 wt.% of benzoic acid, depending on the nature and the amount of the functional groups of the carrier. The size of the benzoic acid particles obtained inside the aerogel matrix depends on the crystallization conditions and is in the range of similar to 20 nm-50 mu m. The crystallinity of the particles was studied and it is shown that the physical state of the loaded benzoic acid inside the pores of aerogels is influenced by benzoic acid-aerogel surface interactions: strong interactions favor the amorphous form, weak interactions favor crystalline particles. The amorphous form of benzoic acid is shown to be stable over a long time period. Thus, silica aerogels can be used for stabilizing amorphous forms of organic compounds, which can be used for instance in pharmaceutical applications for the improvement of drug bioavailability. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:249 / 257
页数:9
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