Thermogravimetry - Differential Scanning Calorimetry

Thermal analysis is a useful tool in the quality control of many incoming routine materials, which can be tested against a reference standard developed internally by analysing a large number of samples of known performance criteria to ensure that the quality of supplies is maintained. Solid elastomers can be identified by glass transition temperature (Tg) [70]. The rubber industry uses thousands of different raw materials, and this number is steadily increasing. These materials are listed in [172]. 

Kodama and co-workers [58] have reported TG-DSC curves for the analysis of the interaction between vulcanisation accelerators (tetramethylthiuram disulphide, dibenzothiazolyl disulphide, diphenylguanidine and N-cyclohexyl-2-benzothiazolyl-sulphenamide) and fillers (carbon black, white carbon, hard clay and CaC03). The initial melting point (MP) of the accelerators was largely influenced by the fillers. The higher the surface activity of the filler is, the lower and wider the melting range becomes. 

Emmott and co-workers [59] have investigated the complex reaction between Sr(N03)2 and the binder Alloprene (a pyrotechnic system) at about 300 °C by simultaneous TG- 

The TG-DSC technique has recently been reviewed [56]. Redfern [57] has reviewed single sample simultaneous thermal analysis, i.e., TG-DSC and TG-DTA studies of polymers. 

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Lopez-Capel, E., Sohi, S., Gaunt, J. L., and Manning, D. A. C. (2005b). Use of thermogravimetry-differential scanning calorimetry to characterize modelable soil organic matter fractions. Am. J. Soil Sci. Soc. 69, 3192-3198. 

The thermal characterisation of elastomers has recently been reviewed by Sircar [28] from which it appears that DSC followed by TG/DTG are the most popular thermal analysis techniques for elastomer applications. The TG/differential thermal gravimetry (DTG) method remains the method of choice for compositional analysis of uncured and cured elastomer compounds. Sircar s comprehensive review [28] was based on single thermal methods (TG, DSC, differential thermal analysis (DTA), thermomechanical analysis (TMA), DMA) and excluded combined (TG-DSC, TG-DTA) and simultaneous (TG-fourier transform infrared (TG-FTIR), TG-mass spectroscopy (TG-MS)) techniques. In this chapter the emphasis is on those multiple and hyphenated thermogravimetric analysis techniques which have had an impact on the characterisation of elastomers. The review is based mainly on Chemical Abstracts records corresponding to the keywords elastomers, thermogravimetry, differential scanning calorimetry, differential thermal analysis, infrared and mass spectrometry over the period 1979-1999. Table 1.1 contains the references to the various combined techniques. 

Thermogravimetry - Differential Scanning Calorimetry - Mass Spectrometry... 

A series of hydrotalcites of general formula Co -M -COg-HT (M " " = Al,Fe and Cr) are prepared by coprecipitation technique. The influence of parameters such as preparation method, atomic ratio, supersaturation levels, aging and hydrothermal treatments are investigated to study their effect on the structure and texture of these materials. The obtained materials are characterised by X-ray diffraction, FT-IR studies, thermogravimetry-differential scanning calorimetry, transmission electron microscopy and BET surface area measurements. Thermal calcination of these materials resulted in the formation of high surface area non-stoichiometric spinels whose catalytic activity is studied using N2O decomposition reaction as the test reaction. The order of activity observed is Co-Al-C03-HT>Co-Fe-C03-HT>Co-Cr-C03-HT. 

I.5.4. Multihyphenated Thermogravimetry-Differential Scanning Calorimetry Techniques... 

Thermal analysis iavolves techniques ia which a physical property of a material is measured agaiast temperature at the same time the material is exposed to a coatroUed temperature program. A wide range of thermal analysis techniques have been developed siace the commercial development of automated thermal equipment as Hsted ia Table 1. Of these the best known and most often used for polymers are thermogravimetry (tg), differential thermal analysis (dta), differential scanning calorimetry (dsc), and dynamic mechanical analysis (dma). 

The procedures of measuring changes in some physical or mechanical property as a sample is heated, or alternatively as it is held at constant temperature, constitute the family of thermoanalytical methods of characterisation. A partial list of these procedures is differential thermal analysis, differential scanning calorimetry, dilatometry, thermogravimetry. A detailed overview of these and several related techniques is by Gallagher (1992). 

The techniques referred to above (Sects. 1—3) may be operated for a sample heated in a constant temperature environment or under conditions of programmed temperature change. Very similar equipment can often be used differences normally reside in the temperature control of the reactant cell. Non-isothermal measurements of mass loss are termed thermogravimetry (TG), absorption or evolution of heat is differential scanning calorimetry (DSC), and measurement of the temperature difference between the sample and an inert reference substance is termed differential thermal analysis (DTA). These techniques can be used singly [33,76,174] or in combination and may include provision for EGA. Applications of non-isothermal measurements have ranged from the rapid qualitative estimation of reaction temperature to the quantitative determination of kinetic parameters [175—177]. The evaluation of kinetic parameters from non-isothermal data is dealt with in detail in Chap. 3.6. 

Fig. 7. Thermogravimetry and differential scanning calorimetry curves for corn cob xylan (Unpublished data).

This paper reviews recycling technologies of PMMA waste, its applications and its markets. It relates in detail experimentation on thermal and oxidative depolymerisation of PMMA scrap, under nitrogen and oxygen atmospheres, at different heating rates by thermogravimetry and differential scanning calorimetry techniques. 15 refs. 

Use of thermogravimetry to facilitate interpretation of differential scanning calorimetry thermograms... 

Thermal analytical techniques such as thermogravimetry (TG), differential thermal analysis (DTA) and differential scanning calorimetry (DSC) have all been successfully employed in studying the pyrotechnic reactions of energetic materials such as black powder, as well as of binary mixtures of the constituents. 

The research papers which originated in the last couple of years in different countries in this field indicate that ED and Er are not generally reported and there is an emphasis on the study of comprehensive thermal behavior of explosives as a function of temperature or time by means of different thermal analytical techniques. Most commonly used methods of thermal analysis are differential thermal analysis (DTA), thermogravimetric analysis (TGA) or thermogravimetry and differential scanning calorimetry (DSC). 

Thermal analysis is a group of techniques in which a physical property of a substance is measured as a function of temperature when the sample is subjected to a controlled temperature program. Single techniques, such as thermogravimetry (TG), differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), dielectric thermal analysis, etc., provide important information on the thermal behaviour of materials. However, for polymer characterisation, for instance in case of degradation, further analysis is required, particularly because all of the techniques listed above mainly describe materials only from a physical point of view. A hyphenated thermal analyser is a powerful tool to yield the much-needed additional chemical information. In this paper we will concentrate on simultaneous thermogravimetric techniques. 

In contrast to polymerisates, polycondensates can not be depolymerized under inert conditions. Decomposition usually leads to the destruction of the chemical structure and the monomers. The thermal decomposition of PET starts at about 300°C in an inert atmosphere [25]. Between 320 and 380°C the main products are acetaldehyde, terephthalic acid, and carbon oxides under liquefaction conditions. The amounts of benzene, benzoic acid, acetophenone, C1-C4 hydrocarbons, and carbon oxides increase with the temperature. This led to the conclusion that a P-CH hydrogen transfer takes place as shown in Eigure 25.8 [26]. Today the P-CH-hydrogen transfer is replaced as a main reaction in PET degradation by several analytic methods to be described in the following sections. The most important are thermogravimetry (TG) and differential scanning calorimetry (DSC) coupled with mass spectroscopy and infrared spectroscopy. 

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