Physicochemical properties of commercial starch hydrolyzates in the frozenstate

Citation
Cg. Biliaderis et al., Physicochemical properties of commercial starch hydrolyzates in the frozenstate, FOOD CHEM, 64(4), 1999, pp. 537-546
Citations number
37
Categorie Soggetti
Food Science/Nutrition
Journal title
FOOD CHEMISTRY
ISSN journal
03088146 → ACNP
Volume
64
Issue
4
Year of publication
1999
Pages
537 - 546
Database
ISI
SICI code
0308-8146(199903)64:4<537:PPOCSH>2.0.ZU;2-0
Abstract
The physical properties of commercial starch hydrolyzate (varying in dextro se equivalent values, DE, from 0.5 to 42) solutions in the frozen state wer e related to their composition. At 20% (w/v) hydrolyzate concentration, an inverse linear relationship between DE and apparent glass transition temper ature (T-g') of the unfrozen solute matrix was observed. The T-g' temperatu res remained relatively constant for solute concentrations below 40% (w/v); above this concentration the T-g' was depressed, possibly due to the plast icizing effect of additional water entrapped in the glassy state during non -equilibrium freezing. Simple predictive models (based on the Flory-Fox equ ation; 1/T-g = Sigma{w(i)/T-gi}) were found to predict reasonably well the T-g' value of 'binary' monodisperse and polydisperse hydrolyzate mixtures o f varying proportions between the two components. Linear relationships were also found between T-g'(measured) (by calorimetry) and T-g'(predicted) (ba sed on the Flory-Fox model, and using the oligosaccharide composition of th e hydrolyzates and the respective T-g' values of the pure components). The rate of oxidation of ascorbic acid has been measured in the presence of sta rch hydrolyzates at temperatures between -4 and -16 degrees C. Both the Arr henius and WLF (Williams-Landel-Ferry) kinetic models were found to describ e the temperature dependence of reaction rate constants reasonably well. Ho wever, knowing the T-g' value of the amorphous maltodextrin was not suffici ent to predict its cryostabilization behavior. (C) 1999 Elsevier Science Lt d. All rights reserved.