Interfacial and foaming properties of prolylenglycol alginates - Effect of degree of esterification and molecular weight

被引:50
作者
Baeza, R
Sanchez, CC
Pilosof, AMR
Patino, JMR
机构
[1] Univ Sevilla, Fac Quim, Dept Ingn Quim, Seville 41012, Spain
[2] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Ind, RA-1428 Buenos Aires, DF, Argentina
关键词
propylene glycol alginate; interfacial activity; surface dilatational properties; adsorption; air-water interface; foaming properties;
D O I
10.1016/j.colsurfb.2004.04.005
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In the present work we have studied the characteristics of propytene glycol alginates (PGA) adsorption at the air-water interface and the viscoelastic properties of the films in relation to its foaming properties. To evaluate the effect of the degree of PGA esterification and viscosity, different commercial samples were studied-Kelcoloid 0 (KO), Kelcoloid LVF (KLVF) and Manucol ester (MAN). The temperature (20degreesC and pH (7.0) were maintained constant. For time-dependent surface pressure measurements and surface dilatational properties of adsorbed PGA at the air-water interface an automatic drop tensiometer was used. The foam was generated by whipping and then the foam capacity and stability was determined. The results reveal a significant interfacial activity for PGA due to the hydrophobic character of the propylene glycol groups. The kinetics of adsorption at the air-water interface can be monitored by the diffusion and penetration of PGA at the interface. The adsorbed PGA film showed a high viscoelasticity. The surface dilatational modulus depends on the PGA and its concentration in the aqueous phase. Foam capacity of PGA solutions increased in the order KO > MAN > KLVF, which followed the increase in surface pressure and the decrease in the viscosities of PGA solutions. The stability of PGA foams monitored by the drainage rate and collapse time follows the order MAN > KLVF > KO. The foam stability depends on the combined effect of molecular weight/degree of esterification of PGA, solution viscosity and viscoelasticity of the adsorbed PGA film. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:139 / 145
页数:7
相关论文
共 25 条
[1]  
Carp DJ, 1997, FOOD SCI TECHNOL-LEB, V30, P253
[2]  
de Feijter J. A., 1987, FOOD EMULSIONS FOAMS, P72
[3]   Hydrocolloids at interfaces and the influence on the properties of dispersed systems [J].
Dickinson, E .
FOOD HYDROCOLLOIDS, 2003, 17 (01) :25-39
[4]  
Dickinson E., 1995, ADV FOOD COLLOIDS, P81
[5]   PROTEINS AT LIQUID INTERFACES .1. KINETICS OF ADSORPTION AND SURFACE DENATURATION [J].
GRAHAM, DE ;
PHILLIPS, MC .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1979, 70 (03) :403-414
[6]  
HORNE DS, 2003, BIOPOLYMERS INTERFAC, P857
[7]   Hydrocolloids in emulsions: particle size distribution and interfacial activity [J].
Huang, X ;
Kakuda, Y ;
Cui, W .
FOOD HYDROCOLLOIDS, 2001, 15 (4-6) :533-542
[8]   Influence of interfacial rheology on foam and emulsion properties [J].
Langevin, D .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2000, 88 (1-2) :209-222
[9]   DYNAMIC MEASUREMENTS OF DILATIONAL PROPERTIES OF A LIQUID INTERFACE [J].
LUCASSEN, J ;
VANDENTE.M .
CHEMICAL ENGINEERING SCIENCE, 1972, 27 (06) :1283-&
[10]  
MARTIN A, 2003, THESIS U WAGENINGEN