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<Emphasis Type="Italic">In situ</Emphasis> monitoring of solid fat content by means of pulsed nuclear magnetic resonance spectrometry and ultrasonics
Authors:Silvana?Martini  Constantin?Bertoli  Maria?Lidia?Herrera  Ian?Neeson  Email author" target="_blank">Alejandro?MarangoniEmail author
Affiliation:(1) Nestlé Research Centre, Lausanne, Switzerland;(2) Departamento de Industrias, Facultad de Ciencias Exactas y Naturales, University of Buenes Aires, Argentina;(3) VN Instruments Ltd., Elizabethtown, Ontario, Canada;(4) Present address: National Research Council of Argentina (CONICET), Argentina;(5) Department of Food Science, University of Guelph, N1G 2W1 Guelph, Ontario, Canada
Abstract:An ultrasonic technique was developed to study the crystallization process of edible fats on-line. A chirp wave was used instead of the conventional pulser signal, thus achieving a higher signal-to-noise ratio. This enabled measurements to be made in concentrated systems ≈20% solid fat content (SFC)] through a 8.11-cm thick sample without significant signal loss. Fat samples were crystallized at 20, 25, and 30°C at a constant agitation rate of 400 rpm for 90 min. The crystallization process was followed by ultrasonic spectroscopy and a low-resolution pulsed nuclear magnetic resonance spectrometer. Specific relationships were found between ultrasonic parameters integrated response, time of flight (TF), and full width half maximum] and SFC. TF, which is an indirect measurement of the ultrasonic velocity (v), was highly correlated to SFC (r 2>0.9) in a linear fashion (v=2.601 SFC+1433.0).
Keywords:Full width half maximum  integrated response  p-NMR  solid fat content  time of flight  ultrasonic velocity
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