摘要

This work examines the polymorphic transition of a glycerol monostearin-water system (GMS-water) stored at 5 degrees C, 25 degrees C and 45 degrees C for 100 days. Upon addition of co-emulsifiers, such as sodium stearoyl lactylate (SSL), the GMS-water system forms a metastable alpha-gel structure, which transforms into a coagel structure over time. The GMS-water system loses its water swelling capacity during the polymorphic transition from the alpha-gel phase to the coagel phase. Therefore the alpha-gel phase is a more favorable structure for water structuring. Powder X-ray diffraction (XRD), XRD with temperature control, differential scanning calorimetry (DSC), and microscopy were used to examine the nature and dynamics of the phase transition. Results suggest that the alpha-gel phase is stable for 100 days when stored at 5 degrees C. Increasing the storage temperature will increase the rate of transformation from the alpha-gel phase to the coagel phase. However, even though no phase transformation from the alpha-gel phase to the coagel phase took place, seemingly, fractionation took place within the alpha-gel structure when stored at 5 degrees C, altering the melting profile of the gel and affecting the calculation of the Coagel index. The GMS-water system forms a thermally reversible and metastable sub-alpha-gel phase when cooled below 13 degrees C. This work characterizes the XRD diffraction patterns and the DSC melting profiles of the sub-alpha-gel phase of GMS-water system for the first time. XRD patterns suggest that the water layer thickness in the sub-alpha-gel phase is similar to 140 angstrom. This thick layer of water may contribute to the high water swelling capacity and stability of the monoglyceride-water system at refrigeration temperatures.

  • 出版日期2014