Abstract
In all DSCs, a temperature difference ΔT — given as a voltage — is the original measurement signal. In almost all instruments a heat flow rate Φ m (differential heat flow rate) is internally assigned to ΔT. Independent of whether the user obtains ΔT or Φ m from the respective DSC, knowledge of the functional relation between the measured signal (ΔT, Φ m ) and the quantity searched (the reaction heat flow rate Φr consumed/produced by the sample) is important for:
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the time-related assignment of Φrto ΔT or Φm(investigation into the kinetics of a reaction),
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the determination of partial heats of reaction,
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the evaluation and assessment of the influences of operating parameters and properties of the measuring system with regard to this relation,
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the estimate of the overall uncertainty of measurement.
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© 1996 Springer-Verlag Berlin Heidelberg
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Höhne, G.W.H., Hemminger, W., Flammersheim, HJ. (1996). Theoretical Fundamentals of Differential Scanning Calorimeters. In: Differential Scanning Calorimetry. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-03302-9_3
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DOI: https://doi.org/10.1007/978-3-662-03302-9_3
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-662-03304-3
Online ISBN: 978-3-662-03302-9
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