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Why are the applications of TGA more limited than those for DSC?

Short Answer

Expert verified

Melting points, crystallizations are some of the thermal transition which is not associated with only change in mass. So TGA is less used in comparison to DSC.

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01

Step 1. Given information

Give the reason for the limited applications of TGA in comparison to DSC.

02

Step 2. Reason for the limited applications of TGA in comparison to DSC 

TGA is one of the thermogravimetric techniques. In this process changes in chemical properties and physical properties are considered as parameters i.e. measuring the mass of the sample is the main characteristic of this process. But in the case of the DSC (differential scanning colorimetry) technique, it is associated with measuring the change in heat. DSC is more used and has a well-developed application in comparison to TGA. Melting points, crystallizations are some of the thermal transition which is not associated with only change in mass. So TGA is less used in comparison to DSC.

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Most popular questions from this chapter

In the pharmaceutical industry, close attention must be paid to drug purity, quality, stability, and safety. Pharmaceutical compounds often have several different structural forms with different molecular shapes. These compounds are also susceptible to thermal degradation, to the pickup and retention of water, and to photodecomposition. One of the best methods to characterize pharmaceuticals from raw product to finished product stage is thermal analysis. The following questions deal with applications of thermal analysis methods to pharmaceuticals.

(a) Determining the purity of drugs is one of the most important tests done by the pharmaceutical industry. One such test is based on a determination of the melting point of the drug of interest by DSC and the following relationship from thermodynamics: d lnX1 dT 5 DHf RT2 where X1 is the mole fraction of the drug whose purity is being determined, DHf is the enthalpy of fusion, R is the gas constant, and T is temperature. From this equation, derive the following modified vanโ€™t Hoff equation: 1 f 5 DHf R 1T0 2 T2 T2 0 1 X0 2 where f is the fraction of sample melting at temperature T, T0 is the melting point of the pure drug, and X0 2 is the mole fraction of the impurity in the original compound. Hint: Assume the drug is close to pure so that ln X1 can be approximated by ln X1 5 ln11 2 X22 < 2X2 As the temperature is increased toward the true melting point T0, the mole fraction in the liquid state X2 is constantly reduced according to X2 5 X0 2 11/f 2

The fraction f can be found from A/AT, where A is the area of the melting endotherm up to temperature T and AT is the total area of the melting endotherm. By dividing the endotherm into partial melting areas, the fraction f can be determined at various temperatures. Rearrange the modified vanโ€™t Hoff equation to give the melting temperature T as a function of 1/f. Show that a plot of T versus 1/f should be linear with an intercept of T0 and a slope of 2RT0X2/DHf. If the heat of fusion is known, X2 can be determined. (c) Look up the article by H. Staub and W. Perron, Anal. Chem., 1974, 46, 128. Give some of the limitations of the DSC approach to impurity determinations. Describe the โ€œstep heatingโ€ method used by the authors. How does this differ from normal DSC? (d) Which type of DSC, power compensated or heat flux, would be most useful in determining purity? Why? (e) What thermal analysis technique would be suitable for characterizing and quantifying the moisture content in a pharmaceutical sample? Why? (f) Describe how thermal analysis could be used to determine the degree of hydration of a pharmaceutical compound. (g) When heated, many pharmaceutical materials show a variety of thermal events, including melting, transitions to glassy states, moisture loss, thermal relaxation, and in some cases, decomposition. How could irreversible kinetic events be distinguished from reversible heat flow events? (h) Describe how microthermal analysis might be useful in studies of pharmaceutical materials. Consider problems such as polymorphic forms, impurities, and identification of glassy states in your answer.

Why is the low-temperature endotherm for ambient pressure in Figure 31-10 found at the same temperature as that at 13.79bar, whereas the high-temperature peaks for the two pressures are found at different temperatures?

Describe what quantity is measured and how the measurement is performed for each of the following techniques: (a) TGA, (b) DTA, (c) DSC, and (d) microthermal analysis.

Describe the difference between power-compensated, heat-flux, and modulated DSC instruments.

The following table summarizes some data about three iron(III) chlorides.

Compound

Molar mass

Melting point in ยฐC

data-custom-editor="chemistry" FeCl3.6H2O

270

37

data-custom-editor="chemistry" FeCl3.52H2O

207

56

data-custom-editor="chemistry" FeCl3

162

306

Sketch the thermogravimetric curve anticipated when a data-custom-editor="chemistry" 25.0-mgsample of role="math" localid="1646289930279" FeCl3.6H2Ois heated fromdata-custom-editor="chemistry" 0ยฐC

to data-custom-editor="chemistry" 400ยฐC.

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