Thermogravimetric decomposition

Estimating the isothermal lifetime of pharmaceutical coatings using thermogravimetric decomposition kinetics... 

Post and co-workers [49] have used TG-FTIR to study the outgassing of a plasticiser (type and amount) from an ethylene-propylene-diene terpolymer (EPDM) compound. Figure 1.6 shows the thermogravimetric decomposition behaviour of the EPDM compound. The plasticiser emerges in the first mass-loss step, which was identified as adipic acid diisobutylester by on-line infrared analysis. 

Figure 1.6 Thermogravimetric decomposition behaviour of an EPDM compound...

ASTM 1877-97, Standard Practice for Calculating Thermal Endurance from Thermogravimetric Decomposition Data. 

Tdecomp represents the onset temperature for thermogravimetric decomposition, arbitrarily defined as the loss of 0.032% of the original sample weight via analysis of the first derivative weight (%/°C) curve. 

T and by dsc, (onset of decomposition) Thermogravimetric analysis ia argon at 10°C heating rate. 

Thermal analysis using differential scanning calorimetry (dsc), thermogravimetric analysis (tga), and differential thermal analysis (dta) can provide useful information about organic burnout, dehydration, and decomposition. 

This phenomenon can be demonstrated by both measuring the changes of the thermal properties of the ECA homopolymer and in adhesion tests. The addition of only 1 wt.% of 9 to a sample of the ECA homopolymer significantly increases the onset of decomposition in the thermogravimetric analysis (TGA) of the polymer, as seen in Fig. 9 [29]. 

Diverse thermogravimetric results can be obtained from samples with different pre-histories for example, TG and DTG curves showed that magnesium hydroxide prepared by precipitation methods has a different temperature of decomposition from that for the naturally occurring material.32 It follows that the source and/or the method of formation of the sample should be ascertained. 

Decomposition of the rare earth nitrates proceeded [821] through the intermediate formation of oxysalts of the form MON03 and E values were low Nd(N03)3, 33 kJ mole 1, 663-703 K Dy(N03)3, 23 kJ mole 1, 583—633 K Yb(N03)3, 46 kJ mole 1, 563—598 K. Thermogravimetric curves showed that the formation of anhydrous salts was possible, in contrast to observations by Wendlandt and Bear [826]. In a similar study [827] of the reaction of Pr(N03)3 at 558—758 K, the intermediate formation of a nitrite is postulated during decomposition to a non-stoichiometric residual oxide, Pr0li83 (the actual composition depends on temperature). 

From infrared and thermogravimetric studies, Pechkovskii et al. [836] identify the following steps in the decomposition of Mg(H2P04)2 2 H20. 

Typical characterization of the thermal conversion process for a given molecular precursor involves the use of thermogravimetric analysis (TGA) to obtain ceramic yields, and solution NMR spectroscopy to identify soluble decomposition products. Analyses of the volatile species given off during solid phase decompositions have also been employed. The thermal conversions of complexes containing M - 0Si(0 Bu)3 and M - 02P(0 Bu)2 moieties invariably proceed via ehmination of isobutylene and the formation of M - O - Si - OH and M - O - P - OH linkages that immediately imdergo condensation processes (via ehmination of H2O), with subsequent formation of insoluble multi-component oxide materials. For example, thermolysis of Zr[OSi(O Bu)3]4 in toluene at 413 K results in ehmination of 12 equiv of isobutylene and formation of a transparent gel [67,68]. 

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