Differential Scanning Calorimetry (DSC) - A Quantitative Thermal Analysis Technique, Assignments of Chemistry

Differential scanning calorimetry (dsc) is a quantitative thermal analysis method used for identifying phase transformations, thermal stabilities, and studying exothermic and endothermic reactions. Unlike temperature gradient analysis (tga) and differential thermal analysis (dta), dsc measures the difference in heat flow between a sample and a reference material as a function of temperature. An introduction to dsc, its principle, history, and differences with dta.

Typology: Assignments

2020/2021

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DIFFERENTIAL SCANNING CALORIMETRY, INTRODUCTION AND
PRINCIPLE
WHY DSC?
Both the thermal techniques which have been discussed so far, TGA and
DTA, are mostly used for qualitative and semi-quantitative analysis.
Information like identification of various substances, phase
transformations, thermal stabilities and study of exothermic and
endothermic reactions can be readily obtained by these techniques.
But in both the cases, as the changes are measured as a function of
temperature, which is not a sensitive parameter to be accurately
measured, hence in analytical terms only semi quantitative data can be
obtained. Better quantitative data can be obtained by using differential
scanning calorimetry (DSC).
PRINCIPLE: Differential Scanning Calorimetry (DSC) is not much
different technique than DTA. In DSC also the sample is heated along
with a reference material through a programmed temperature range.
However, in the case of a change in the sample, the temperature
difference between the sample and the reference can be compensated
by providing extra thermal energy either to the sample or to reference.
This additional energy, usually in form of electric current, which is
provided to keep the sample and the reference at equal temperatures is
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DIFFERENTIAL SCANNING CALORIMETRY, INTRODUCTION AND

PRINCIPLE

WHY DSC?

Both the thermal techniques which have been discussed so far, TGA and DTA, are mostly used for qualitative and semi-quantitative analysis. Information like identification of various substances, phase transformations, thermal stabilities and study of exothermic and endothermic reactions can be readily obtained by these techniques. But in both the cases, as the changes are measured as a function of temperature, which is not a sensitive parameter to be accurately measured, hence in analytical terms only semi quantitative data can be obtained. Better quantitative data can be obtained by using differential scanning calorimetry (DSC). PRINCIPLE: Differential Scanning Calorimetry (DSC) is not much different technique than DTA. In DSC also the sample is heated along with a reference material through a programmed temperature range. However, in the case of a change in the sample, the temperature difference between the sample and the reference can be compensated by providing extra thermal energy either to the sample or to reference. This additional energy, usually in form of electric current, which is provided to keep the sample and the reference at equal temperatures is

measured accurately. This electrical energy serves as an exact measure of the change occurred in the sample. HISTIRY: The technique was developed by E.S. Watson and M.J. O’Neill in 1962. This was introduced commercially at Pittsburgh Conference on Analytical Chemistry and Applied Spectroscopy in 1963. The first differential scanning calorimeter that could be used in biochemistry was developed by P.L. Privalov and D.R. Monaselidze in 1964 at Institute of Physics in Tbilisi, Georgia. Differential scanning calorimetry (DSC) is the most often used thermal analysis method, primarily because of its speed, simplicity, and availability. PRINCIPLE: DSC is one of the thermal techniques wherein difference in heat flow into substance and reference material is measured as a function of sample temperature when both substances are exposed to controlled temperature. The output is measured and plotted against temperature or time to get a thermogram. PRINCIPLE: In DSC a sample and a reference are placed in holders in the instrument. Heaters either ramp the temperature at a specified rate (e.g., 5 0 C/min) or hold the DSC at a given temperature. The instrument measures the difference in the heat flow between the sample and the reference. The basic difference between DSC and DTA is that DSC is a