Thermal and structural behavior of anhydrous milk fat. 3. Influence of cooling rate

Abstract

The crystallization behavior of anhydrous milk fat has been examined with a new instrument coupling time-resolved synchrotron x-ray diffraction as a function of temperature (XRDT) at both small and wide angles and high-sensitivity differential scanning calorimetry. Crystallizations were monitored at cooling rates of 3 and 1°C/ min from 60 to –10°C to determine the triacylglycerol organizations formed. Simultaneous thermal analysis permitted the correlation of the formation/melting of the different crystalline species monitored by XRDT to the thermal events recorded by differential scanning calorimetry. At intermediate cooling rates, milk fat triacylglycerols sequentially crystallize in 3 different lamellar structures with double-chain length of 46 and 38.5 Å and a triple-chain length of 72 Å stackings of {alpha} type, which are correlated to 2 exothermic peaks at 17.2 and 13.7°C, respectively. A time-dependent slow sub-{alpha} {leftrightarrow} {alpha} reversible transition is observed at –10°C. Subsequent heating at 2°C/min has shown numerous structural rearrangements of the {alpha} varieties into a single ß' form before final melting. This polymorphic evolution on heating, as well as the final melting point observed (~39°C), confirmed that cooling at 3°C/min leads to the formation of crystalline varieties that are not at equilibrium. An overall comparison of the thermal and structural properties of the crystalline species formed as a function of the cooling rate and stabilization time is presented. The influence on crystal size of the cooling rates applied in situ using temperature-controlled polarized microscopy is also determined for comparison