Nitrogen sorption as a tool for the characterisation of polysaccharide aerogels

被引:64
作者
Robitzer, M. [1 ]
Tourrette, A. [1 ]
Horga, R. [1 ]
Valentin, R. [1 ]
Boissiere, M. [1 ]
Devoisselle, J. M. [1 ]
Di Renzo, F. [1 ]
Quignard, F. [1 ]
机构
[1] ENSCM, Inst Charles Gerhardt Montpellier, CNRS, UMR 5253,UM2,UM1, F-34296 Montpellier 5, France
关键词
Aerogel; Supercritical drying; Comparison plots; Surface polarity; Adsorption enthalpy; Physisorption; Polysaccharides; Alginate; Chitosan; Chitin; Agar; Carrageenan; TEMPERATURE ELECTRON-MICROSCOPY; X-RAY-DIFFRACTION; BACTERIAL ADHESION; SURFACE-AREA; CELL-WALL; ALGINATE AEROGELS; CONTACT-ANGLE; CHITOSAN; ADSORPTION; HYDROGELS;
D O I
10.1016/j.carbpol.2011.01.040
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Supercritically dried aerogels of several polysaccharides (chitin, chitosan, alginate, alginic acid, kappa-carrageenan, and agar) have been characterised by physisorption of N-2. Surface areas as high as 570 m(2) g(-1) have been measured. The nature of the functional groups of the polysaccharide significantly influences the adsorption of N2 on the surface of the aerogel. The net enthalpy of adsorption increases with the polarity of the surface groups of the polymer, in the order chitin < agar <= chitosan < carrageenan < alginic acid similar to alginate. The surface area and the mesopore distribution of the aerogels depend both on the dispersion of the parent hydrogel and on the behaviour of each polymer in the drying treatment. Aerogels which retain the dispersion of the parent hydrogel are mainly macroporous (pores larger than 50 nm) while materials liable to shrink upon solvent exchange form mesoporous structures. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:44 / 53
页数:10
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