Detection Differential scanning calorimetry

Crystallinity in ECH and ECH—EO finished products increases over time, and may be detected by x-ray analysis or differential scanning calorimetry. In synthesizing ECH—EO, the process is designed to maximize random monomer sequence and minimize crystallinity. The ECH—EO molecular ratio in these products ranges from approximately 3 1 to 1 1. 

Triethanolamine salts of alcohol sulfates form white crystals when obtained in pure form after recrystallization. At their melting point they are semisolid with gelatinous appearance and the transition is difficult to detect. Melting points, determined through thermograms obtained by differential scanning calorimetry, gave 72, 76, 80, and 86°C for dodecyl, tetradecyl, hexadecyl, and octadecyl sulfates, respectively [63]. 

Structured proteins have also been investigated by thermal analysis [40,41], denaturing resulting in an endotherm which is readily detected by differential scanning calorimetry (DSC). DSC of recombinant resilin in the swollen state showed no transitions over a wide temperature range (25°C-140°C), further evidence of the absence of any strucmre. This is in contrast to the strucmred proteins wool and bovine serum albumin, which show denamration endotherms at 145°C and 62°C, respectively (Figure 9.6). 

A 100 Degree Rule was often used in the past throughout the chemical industry to assess whether an accident would occur. According to this rule, if the operating temperature of a process is 100 "C away from the nearest detectable exotherm observed in DSC (Differential Scanning Calorimetry) experiment the operation will not experience this thermal event. In such a case no more detailed information on hazards need be searched for. The 100°C degree rule is, however, often far from the safety margin The use of this rule was the reason of many accidents. 

One such property, as has been demonstrated (see [26]), is the change in partial heat capacity of the copolymer solution upon the heat-induced conformational transition of macromolecules. Such a change was detected by high-sensitivity differential scanning calorimetry (HS-DCS). The DSC data for the NVCl/NVIAz-copolymers synthesized at initial comonomer ratios of 85 15 and 90 10 (mole/mole) are given as thermograms in Fig. 4. 

Differential scanning calorimetry (DSC) and x-ray diffraction (XRD) are the techniques most widely used for the characterization of crystallinity and polymorphism of solid lipid particles. Although DSC is usually more sensitive in detecting crystalline material, XRD is much more reliable in determining the type of polymorph present in the dispersions because it provides structural data. In contrast, DSC can detect the type of polymorph only indirectly via the transition temperatures and enthalpies. Because these parameters may be different from those observed in the bulk material, particularly for small colloidal particles [1,62], assigmnent of polymorphic forms in DSC curves should be supported by x-ray data. 

Next, the thermal properties of the dye must be such that absorption of the laser energy will result in dye diffusion but not in decomposition. The melting temperature Tm, the latent heat of fusion, AH, and the specific heat for these dyes were determined by differential scanning calorimetry using a DuPont 990 Thermal Analyzer. The data are given in Table II. No thermal decomposition products for these dyes were detected upon heating to 600 °C for 20 msec. 

Various techniques might be used to detect such a two-dimensional melt in membranes, but differential scanning calorimetry (DSC) is particularly useful because membranes can be examined under physiological conditions and results can be made quantitative in a straightforward manner. In DSC a sample and a thermally inert reference (lacking a transition) are both heated at a constant rate. The measured parameter is the difference in power input between the sample and reference necessary to maintain identical heating rates for both. If no... 

Differential scanning calorimetry can be used to detect isosorbide dinitrate in the presence of various proportions of other isohexide mononitrates in pharmaceutical formulations81 and for testing its hazardous characteristics.82 A complete analytical profile for isosorbide dinitrate, detailing spectroscopic and other physical properties, as well as useful analytical methods, has been reported.83... 

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