Hydroxypropylmethylcellulose surface activity at equilibrium and adsorption dynamics at the air-water and oil-water interfaces

被引:63
|
作者
Camino, Nerina A. [1 ,2 ]
Perez, Oscar E. [1 ,2 ]
Carrera Sanchez, Cecilio [3 ]
Rodriguez Patino, Juan M. [3 ]
Pilosof, Ana M. R. [1 ,2 ]
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Ind, RA-1428 Buenos Aires, DF, Argentina
[2] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
[3] Univ Seville, Dept Ingn Quim, Fac Quim, E-41012 Seville, Spain
关键词
Hydroxypropylmethylcellulose; Polysaccharide; Adsorption; Air-water interface; Oil-water interface; HYDROXYPROPYL-METHYL-CELLULOSE; ADSORBED FILMS; DILATIONAL BEHAVIOR; PROTEINS; METHYLCELLULOSE; KINETICS; POLYSACCHARIDES; GELATION; TENSION;
D O I
10.1016/j.foodhyd.2009.06.013
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The surface behaviour of hydroxypropylmethylcelluloses (HPMC) was studied at the air-water (A/W) and oil-water (O/W) interfaces. At the A/W interface, the pi-C isotherms were sigmoidal and presented inflexions as the HPMC bulk concentration increases, related with different structural patterns adopted by the biopolymer segments. The behaviour of these biopolymers at the O/W interface resulted different. No inflections in the adsorption isotherm were observed, denoting the absence of any change in the structure of the adsorbed monolayer. The order in the interfacial activity was different at the two interfaces. The dynamics of adsorption showed that the surface pressure (pi) values and the rate of adsorption/penetration were lower at the O/W interface. Analogously to pi values, the surface dilatational modulus was smallest at the O/W interface, however at long-term adsorption strong viscoelastic films are formed at the O/W interface. (C) 2009 Elsevier Ltd. All rights reserved.
引用
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页码:2359 / 2368
页数:10
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