Dynamics of adsorption of hydroxypropyl methylcellulose at the air-water interface

被引:70
|
作者
Pérez, Oscar E.
Sánchez, Cecilio Carrera
Pilosof, Ana M. R.
Patino, Juan M. Rodriguez
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Ind, RA-1428 Buenos Aires, DF, Argentina
[2] Univ Seville, Fac Quim, Dept Ingn Quim, E-41012 Seville, Spain
关键词
polysaccharide; hydroxypropyl methylcellulose; biopolymer; air-water interface; surface rheology; adsorption; surface pressure; surface; dilatational properties; brewster angle microscopy;
D O I
10.1016/j.foodhyd.2006.12.005
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Surface dynamic properties (surface pressure and surface dilatational properties) of three commercial hydroxypropyl methylcellulose (HPMC adsorbed at the air-water interface are presented in this paper as a function of adsorption time. Experiments were performed at constant temperature (20 degrees C, pH 7, and ionic strength 0.05 M. The dynamics of adsorption and the surface dilatational properties were measured simultaneously for different food-grade HPMC (called E4M, E50LV, and F4M), at bulk concentrations (C-HPMC) ranging from 1 x 10(-4) to 1% wt. It was found that the surface pressure (pi) increased with the HPMC bulk concentration, which may be associated with HPMC adsorption. These phenomena have been related to HPMC diffusion to the interface (at short adsorption time) and to molecular interactions (at long-term adsorption). The HPMC films behaved as viscoelastic as deduced from the surface dilatational elasticity (E-d) and the loss angle tangent (Tan delta) evolution upon time. The values of E-d showed different behavior with the HPMC bulk concentration, which reflect structural differences in the adsorbed film. Differences in the dynamics of adsorption and surface dilatational properties between different HPMCs have been related to molecular differences, such as the molecular weight, degree of substitution, molar substitution, etc. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:387 / 402
页数:16
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