Thermal decomposition of CoC2O4⋅2H2O was studied using DTA, TG, QMS and XRD techniques. It was shown that decomposition generally occurs in two steps: dehydration
to anhydrous oxalate and next decomposition to Co and to CoO in two parallel reactions. Two parallel reactions were distinguished
using mass spectra data of gaseous products of decomposition. Both reactions run according toAvrami–Erofeev equation. For
reaction going to metallic cobalt parameter n=2 and activation energy is 9714 kJ mol–1. It was found that decomposition to CoO proceeds in two stages. First stage (0.12<αII<0.41) proceeds according to n=2, with activation energy 25115 kJ mol–1 and second stage (0.45<αII<0.85) proceeds according to parameter n=1 and activation energy 20321 kJ mol–1.
Thermal decomposition of natural pyrite (cubic, FeS2) has been investigated using X-ray diffraction and57Fe Mössbauer spectroscopy. X-ray diffraction analysis of pyrite ore from different sources showed the presence of associated minerals, such as quartz, szomolnokite, stilbite or stellerite, micas and hematite. Hematite, maghemite and pyrrhotite were detected as thermal decomposition products of natural pyrite. The phase composition of the thermal decomposition products depends on the temperature, time of heating and starting size of pyrite crystals. Hematite is the end product of the thermal decomposition of natural pyrite.
The thermal stability of polypyrrole
(PPy) samples has been studied by thermogravimetry/mass spectrometry and pyrolysis-gas
chromatography/mass spectrometry in inert atmospheres. PPy has been prepared
by chemical oxidative polymerization using ferric sulfate as an oxidant and
anionic surfactants, such as dodecylbenzenesulfonic acid and sodium dodecylbenzenesulfonate
as co-dopants. For comparison we have studied polypyrrole (PPy-SO4)
prepared without any additive. It was found that the presence of anionic surfactants
improved the thermal stability of PPy. The decomposition of PPy doped with
ferric sulfate and anionic surfactants occurs at relatively high temperature
indicating that chemical interactions exist between the polymer and the surfactants.
For the quantitative analyses of evolved CO2and H2O during the thermal decomposition of solids, calibration curves, i.e. the amounts of evolved gases vs. the corresponding
peak areas of mass chromatograms measured by TG-MS, were plotted as referenced by the reaction stoichiometry of the thermal
decomposition of sodium hydrogencarbonate NaHCO3. The accuracy and reliability of the quantitative analyses of the evolved CO2and H2O based on the calibration curves were evaluated by applying the calibration curves to the mass chromatograms for the thermal
decompositions of copper(II) and zinc carbonate hydroxides. It was indicated from the observed ratio of evolved CO2and H2O that the compositions of copper(II) and zinc carbonate hydroxides examined in this study correspond to mineral malachite,
Cu2CO3(OH)2, and hydrozincate, Zn5(CO3)2(OH)6, respectively. Reliability of the present analytical procedure was confirmed by the fairly good agreement of the mass fraction
of the evolved gases calculated from the analytical values with the total mass-loss during the thermal decompositions measured
Solid M-Ox compounds, whereM represents Mg(II), Zn(II), Pb(II) and NbO(III), and Ox is 8-quinolinol, have been prepared. Thermogravimetry, derivative
thermogravimetry (TG, DTG), differential scanning calorimetry (DSC), nuclear magnetic resonance (NMR) and infrared absorption
spectra (IR) have been used to characterize and to study the thermal stability and thermal decomposition of these compounds.
multivalent platinum drug based on a poly(amidoamine) [PAMAM] dendrimer (generation
4.5, carboxylate surface) has been synthesized and fully characterized using
a variety of spectroscopic, chromatographic and thermal methods. Treatment
of the dendrimer with an aqueous solution containing an excess diaquo(cis-1,2-diaminocyclohexane)platinum(II) produces
a conjugate containing approximately forty (diaminocyclohexane)platinum(II)
moieties at the surface of the dendrimer. This material undergoes smooth two-stage
thermal decomposition to provide residual platinum oxide reflecting the platinum
loading in the drug.
The present work investigates
the influence of milling and calcination atmosphere on the thermal decomposition
of SrTiO3 powder precursors. Both pure and neodymium-modified SrTiO3 samples
were studied. Milling did not significantly influence numerical mass loss
value, but reduced the number of decomposition steps, modifying the profiles
of the TG and DTA curves. On the other hand, milling increases the amount
of energy liberated by the system upon combustion of organic matter. It was
also observed that the milling process, associated to the calcination in an
oxygen atmosphere, considerably decreases the amount of organic matter and
increases the final mass loss temperature.
Detailed analysis of the results of full potential linearized augmented plane wave (FP LAPW) ab initio calculations for anhydrous silver and cadmium oxalates, reported in first part of this paper  has been presented. Additional
calculations of Bader’s AIM (Atoms in Molecules) topological properties of the electron density, bond orders (Pauling, Bader,
Cioslowski and Mixon) and bond valences according to bond valence model have been done. The obtained results show the similarities
in electronic structure of both compounds and support the conclusion, that during the thermal decomposition process, these
compounds should most probably decompose to metal and carbon dioxide, in agreement with the experiment.
Thermal decomposition of M(mal/fum)�xH2O (M=Mn, Co, Ni) has been studied in static air atmosphere from ambient to 500�C employing TG-DTG-DTA, XRD and IR spectroscopic
techniques. After dehydration the anhydrous maleate salts decompose to metal oxalate in the temperature range of 320–360�C,
which at higher temperature undergo an abrupt oxidative pyrolysis to oxides. The anhydrous fumarate salts have been found
to decompose directly to oxide phase. A comparison of thermal analysis reveals that fumarates are thermally more stable than
The thermal decomposition of Eu2(BA)6(bipy)2 (BA=C2H5N–2, benzoate; bipy=C10H8N2, 2,2'-bipyridine)and its kinetics were studied under the non-isothermal condition by TG-DTG, IR and SEM methods. The kinetic
parameters were obtained from analysis of the TG-DTG curves by the Achar method, the Madhusudanan-Krishnan-Ninan (MKN) method,
the Ozawa method and the Kissinger method. The most probable mechanism function was suggested by comparing the kinetic parameters.
The kinetic equation for the first stage can be expressed as: dα/dt=Aexp(–E/RT)3(1–α)2/3.