Some physical changes associated with the development of Maillard reaction in a glucose-glycine aqueous solution were detected by means of thermal and rheological analysis as well as by more conventional determinations. The increase in water content, water activity (A(w)) and enthalpy of ice melting (Delta Hm) during the reaction reflects both the formation of new water molecules and the consumption of low molecular weight species. The concomitant arrangement of more complex molecular structures was indicated by changes in the glass transition temperature of the maximally freeze-concentrated solution (Tg') and of the freeze-dried solution (Tg((dry))) as well as in the estimated unfrozen water (UFW). After fractionation of the samples by solid phase extraction, the nonpolar fractions exhibited much higher Tg((dry)) than the non-fractionated samples. The Tgs((dry)) of samples at increasing heating time were treated with the Gordon-Taylor equation add results were discussed. The expected increase in viscosity due to polymerisation was compensated by the formation of water, but it could be detected when viscosities were measured on samples equilibrated at a same A(w)
Physical changes induced by the Maillard reaction in a glucose-glycine solution
MANZOCCO, Lara;MALTINI, Enrico
1999-01-01
Abstract
Some physical changes associated with the development of Maillard reaction in a glucose-glycine aqueous solution were detected by means of thermal and rheological analysis as well as by more conventional determinations. The increase in water content, water activity (A(w)) and enthalpy of ice melting (Delta Hm) during the reaction reflects both the formation of new water molecules and the consumption of low molecular weight species. The concomitant arrangement of more complex molecular structures was indicated by changes in the glass transition temperature of the maximally freeze-concentrated solution (Tg') and of the freeze-dried solution (Tg((dry))) as well as in the estimated unfrozen water (UFW). After fractionation of the samples by solid phase extraction, the nonpolar fractions exhibited much higher Tg((dry)) than the non-fractionated samples. The Tgs((dry)) of samples at increasing heating time were treated with the Gordon-Taylor equation add results were discussed. The expected increase in viscosity due to polymerisation was compensated by the formation of water, but it could be detected when viscosities were measured on samples equilibrated at a same A(w)File | Dimensione | Formato | |
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