4.7 Article

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

Journal

JOURNAL OF DAIRY SCIENCE
Volume 88, Issue 2, Pages 511-526

Publisher

ELSEVIER SCIENCE INC
DOI: 10.3168/jds.S0022-0302(05)72713-2

Keywords

triacylglycerol; polymorphism; differential scanning calorimetry; x-ray diffraction

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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 1degreesC/min from 60 to -10degreesC 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 Angstrom and a triple-chain length of 72 Angstrom stackings of alphaa type, which are correlated to 2 exothermic peaks at 17.2 and 13.7degreesC, respectively. A time-dependent slow sub-alpha <----> alpha reversible transition is observed at -10degreesC. Subsequent heating at 2degreesC/min has shown numerous structural rearrangements of the alpha varieties into a single beta' form before final melting. This polymorphic evolution on heating, as well as the final melting point observed (-39degreesC), confirmed that cooling at 3degreesC/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.

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