Kinetics of non-isothermal decomposition of cinnamic acid

The thermal stability and kinetics of decomposition of cinnamic acid were investigated by thermogravimetry and differential scanning calorimetry at four heating rates. The activation energies of this process were calculated from analysis of TG curves by methods of Flynn-Wall-Ozawa, Doyle, Distributed Activation Energy Model, ?atava-?esták and Kissinger, respectively. There are only one stage of thermal decomposition process in TG and two endothermic peaks in DSC. For this decomposition process of cinnamic acid, E and logA[s^?1] were determined to be 81.74 kJ mol^?1 and 8.67, respectively. The mechanism was Mampel Power law (the reaction order, n = 1), with integral form G(α) = α (α = 0.1–0.9). Moreover, thermodynamic properties of ΔH ^≠, ΔS ^≠, ΔG ^≠ were 77.96 kJ mol^?1, ?90.71 J mol^?1 K^?1, 119.41 kJ mol^?1.     

Kinetics of the non-isothermal decomposition of Cu-and Co-itaconato complexes

The kinetics of the thermal decomposition of Cu- and Co-itaconato complexes were studied using dynamic thermogravimetric techniques. The dehydration process was found to proceed in a one-stage reaction, while the thermal decomposition of the anhydrous salts was followed a two-stage reaction. The first stage is the decomposition of the complex to metal carbonate, whereas the second stage is the decomposition of the formed carbonate to the oxide. Kinetic analysis of the dynamic TG curves were discussed with reference to a composite integral method on comparison with the integral methods of Coats and Redfern and Ozawa. The activation parameters were calculated and discussed for each decomposition step.     

Kinetic of decomposition of some complexes under non-isothermal conditions

Kinetics of thermal decomposition of three structurally similar complexes Co₂Cu(C₂O₄)₃ (R-diam)₂, where R is ethyl, 1,2-propyl or 1,3-propyl, was studied under non-isothermal conditions and nitrogen dynamic atmosphere at heating rates of 5, 7, 10, 12 and 15 K min⁻¹. For data processing the Flynn-Wall-Ozawa and a modified non-parametric kinetic methods were used. By both methods the activation energy are in the range of 97–102 kJ mol⁻¹. The formal kinetic is r=kα(1−α)². Also a compensation effect between lnA and E was evidenced. The kinetic analysis lead to the conclusion of an identic decomposition mechanism by a single step process.     

Kinetics of the non-isothermal decomposition of some metal hippurates from DTG curves

Calculated vapor pressures have been used to estimate the composition of the vapor over an equimolar mixture of linear alkanes and to make inferences about the effects of pressure on the thermal degradation of polyethylene as studied using thermogravimetry. The troublesome bubbling in molten PE degrading under vacuum conditions has been related to the boiling out of molecules in the range C₃₀ to >C₈₀. The effect of pressure in lowering the apparent overall activation energy has been ascribed to contributions from the lalent heats of vaporization of molecules in the range C₁₅ to ～C₃₀.     

Thermal decomposition of decavanadates of bivalent metals

The thermal decomposition of Cd₃V₁₀O₂₈ · 16H₂O and Mg₃V₁₀O₂₈ · 18H₂O has been investigated. It was found by means of IR spectroscopy and X-ray phase analysis that the final products of decomposition of the given compounds are V₂O₅, the corresponding metavanadates and the vanadium bronzes of cadmium and magnesium. Present and previous results allow conclusions on the thermal decomposition of decavanadates of bivalent metals.

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Zusammenfassung Die thermische Zersetzung von Cd₃V₁₀O₂₈ · 16 H₂O und Mg₃V₁₀O₂₈ · · 18 H₂O wurde untersucht. Durch IR-Spektroskopie und Röntgen-Phasenanalyse wurde festgestellt, daß die Endprodukte der Zersetzung der gegebenen Verbindungen V₂O₅ ist, entsprechend den Metavanadate und den Vanadiumbronze von Cadmium und Magnesium. Die gegenwärtigen und früheren Ergebnisse gestatten Folgerungen bezüglich der thermischen Zersetzung von Dekavanadaten zweiwertiger Metalle.

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Résumé On a étudié la décomposition thermique de Cd₃V₁₀O₂₈ · 16 H₂O et Mg₃V₁₀O₂₈ · · 18 H₂O. A l'aide des techniques de spectroscopie IR et de rayon X, on a établi que les produits finaux de la décomposition de ces composés sont V₂O₅, les métavanadates correspondants et les bronzes au vanadium, de cadmium et magnésium. Les résultats présents et antérieurs permettent de tirer des conclusions sur la décomposition thermique des décavanadates des métaux divalents.

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d₃V₁₀₂₈ · 16₂ Mg₃V₁₀O₂₈· 18H₂O. , , V₂O₅, . , , .

     

Stability constants of some bivalent metal complexes of N-phenyl-o-tolylbenzohydroxamic acid

The stability constants of the Cu²⁺, Zn²⁺, Ni²⁺ and Mu²⁺ complexes of N-phenyl-o-methoxybenzohydroxamic acid at 30° in 50% v/v aqueous dioxan are: log K₁ 10·45, 8·16, 7·52, 6·33; log K₂ 8·90, 6·70, 6·01, 5·59 (for the ions in the order given).     

Kinetics of non-isothermal decomposition of three IRGANOX-type antioxidants

In the present work a comparative kinetic study was performed on the thermal behavior of three antioxidants of IRGANOX-type (L101, L109 and L115) in dynamic air atmosphere under non-isothermal conditions. The TG-DTG data were obtained at heating rates of 5, 7, 10 and 15 K min⁻¹. The kinetic parameters were obtained by processing these data with strategies corresponding to Flynn-Wall-Ozava (FWO), Friedman (FR), Budrugeac-Segal (BS) and non-parametric kinetic (NPK) methods. The thermal degradation by all the three compounds take place in melted state, so that any kinetic models regarding the decomposition of solids are inapplicable. Only with the NPK method it was possible a separation between the two functions of the reaction rate. For the temperature dependence, f(T), an Arrhenius-type model was searched; for the conversion dependence, the Ŝestak-Berggren equation was suggested in order to discriminate between physical (m) and chemical (n or p) steps of a complex thermodegradation process.     

氨合氯化镁非等温热分解过程动力学研究

由有机溶剂法得到的中间产物氨合氯化镁[1]制备电解炼镁的无水氯化镁,煅烧过的程中的条件对无水氯化镁的纯度有较大的影响.     

Kinetics of non-isothermal crystallization of some glass-ceramics based on basalt

The crystallization kinetics of some glass-ceramics obtained from Romanian (Şanoviţa) basalt has been studied in non-isothermal conditions using DTA technique. The activation energies of the crystallization processes were calculated using the isoconversional methods Kissinger-Akahira-Sunose and Ozawa-Flynn-Wall. The results obtained show a dependence of the activation energy (E _α) on the crystallized fraction (α) that proves the complex mechanism of the glass-ceramics crystallization process. It has been proved that the Johnson-Mehl-Avrami model cannot be applied for the studied glass-ceramics crystallization process. The effect of 2% TiO₂ as nucleating agent upon the crystallization kinetics and upon the microstructure of the studied glass-ceramics was analyzed.     

Kinetics of thermal decomposition of trivalent metal complexes with all-cis-1,2,3,4-cyclopentane tetracarboxylic acid

All-cis-1, 2, 3, 4-cyclopentane tetracarboxylic acid forms 11 complexes with metals like Al(III), Y(III) and Ga(III), and have been isolated in solid state from the aqueous solutions. Thermogravimetry of these complexes supports the probable formulae assigned on the basis of elemental analysis. Kinetics of some of the thermal decompositions have been studied. Various kinetic parameters such as apparent activation energy, order of decomposition, frequency factor and activation entropy have been evaluated and the former two constants have been compared by two methods and are in reasonable agreement with each other.

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Zusammenfassung All-cis-l,2,3,4-Cyclopentantetracarbonsäure bildet 11 Komplexe mit Metallen wie Al(III), Y(III) und Ga(III). Sie wurden in festem Zustand aus den wässerigen Lösungen isoliert. Die Thermogravimetrie dieser Komplexe unterstützt die wahrscheinlichen Formeln, welche den Verbindungen auf Grund der Elementaranalyse Zugeschrieben worden sind. Die Kinetik einiger dieser thermischen Zersetzungen wurde untersucht. Verschiedene kinetische Parameter, wie die scheinbare Aktivierungsenergie, die Ordnung der Zersetzung, der Frequenzfaktor und die Aktivierungsentropie wurden bewertet und die ersten beiden Konstanten mittels zweier Methoden verglichen und in guter Übereinstimmung mit einander gefunden.

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Résumé L'acide all-cis-l,2,3,4-cyclopentanetétracarboxylique forme des complexes 11 avec les métaux tels que Al(III), Y(III) et Ga(III) et a été isolé à l'état solide à partir des solutions aqueuses. La thermogravimétrie de ces complexes vient à l'appui des formules probables établies par l'analyse élémentaire. La cinétique de la décomposition thermique de plusieurs d'entre eux a été étudiée. Divers paramètres cinétiques comme l'énergie d'activation, l'ordre de la décomposition, le facteur de fréquence et l'entropie d'activation ont été évalués. La comparaison des deux premières constantes obtenues par deux méthodes différentes montre une très bonne concordance des valeurs.

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--1,2,3,4- 1(III), (III) Ga(III) 11, . , . . , , , , , .

     

Kinetic study of the thermal decomposition of heterocyclic thiol complexes under non-isothermal conditions

The thermal decomposition in the solid-phase has been studied by thermogravimetric (TG) and differential thermal analysis (DTA) techniques for a number of heterocyclic thiol complexes. The method of Coats and Redfern was used to study the kinetics of the thermal decomposition process. The enthalpy changes and activation energies for the decomposition have been calculated.

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Zusammenfassung Die thermische Zersetzung in fester Phase wurde an einigen heterozyklischen Thiolkomplexen mit den Methoden der dynamischen Thermogravimetrie (TG) und der Differentialthermoanalyse (DTA) untersucht. Die Methode von Coats und Redfern wurde zum Studium der Kinetik des thermischen Zersetzungsvorganges eingesetzt. Die Enthalpie-Änderungen und Aktivierungsenergien der Zersetzung wurden berechnet.

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Résumé Etude de la décomposition thermique en phase solide de plusieurs complexes thiols hétérocycliques par thermogravimétrie (TG) et par analyse thermique différentielle (ATD). La méthode de Coats et Redfern a été appliquée pour déterminer la cinétique du processus de la décomposition thermique. Les variations d'enthalpie et les énergies d'activation de la décomposition ont été calculées.

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(TG) (DTA) . . .

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We are grateful to Prof. K. C. Joshi, Head of the Chemistry Department and Dr. A. K. Rai of Rajasthan University, Jaipur for permitting the generous use of the thermorecording balance at the University and to Dr. E. R. Saxena, Assistant Director, Mineral Products and Inorganic Chemicals Division and Mr. P. Narayanachar of Regional Research Laboratory, Hyderabad for their valuable assistance in taking DTA trace. Thanks are also due to Prof. V. V. S. Murti, Head of the Chemistry Department, University of Delhi for his interest in the work. The author (K. A. V.) thanks the University Grants Commission, New Delhi for the award of the fellowship under which these investigations have been carried out.     

Kinetics of exothermal decomposition of 2-nitrophenylhydrazine and 4-nitrophenylhydrazine using DSC non-isothermal data

Kinetics of exothermal decomposition of 2-nitrophenylhydrazine (2-NPH) and 4-nitrophenylhydrazine (4-NPH) was investigated by differential scanning calorimetry. The isoconversional methods, Friedman and Flynn-Wall-Ozawa, were applied to determine the activation parameters from the common analysis of multiple curves measured at different heating rates. For the processes involving two-step reactions the multivariate non-linear regression was used. A good agreement between the experimental and the fitted data was found.     

Thermal decomposition and non-isothermal decomposition kinetics of carbamazepine

The thermal stability and kinetics of isothermal decomposition of carbamazepine were studied under isothermal conditions by thermogravimetry (TGA) and differential scanning calorimetry (DSC) at three heating rates. Particularly, transformation of crystal forms occurs at 153.75°C. The activation energy of this thermal decomposition process was calculated from the analysis of TG curves by Flynn-Wall-Ozawa, Doyle, distributed activation energy model, ?atava-?esták and Kissinger methods. There were two different stages of thermal decomposition process. For the first stage, E and logA [s^?1] were determined to be 42.51 kJ mol^?1 and 3.45, respectively. In the second stage, E and logA [s^?1] were 47.75 kJ mol^?1 and 3.80. The mechanism of thermal decomposition was Avrami-Erofeev (the reaction order, n = 1/3), with integral form G(α) = [?ln(1 ? α)]^1/3 (α = ～0.1–0.8) in the first stage and Avrami-Erofeev (the reaction order, n = 1) with integral form G(α) = ?ln(1 ? α) (α = ～0.9–0.99) in the second stage. Moreover, ΔH ^≠, ΔS ^≠, ΔG ^≠ values were 37.84 kJ mol^?1, ?192.41 J mol^?1 K^?1, 146.32 kJ mol^?1 and 42.68 kJ mol^?1, ?186.41 J mol^?1 K^?1, 156.26 kJ mol^?1 for the first and second stage, respectively.     

Studies on the thermal decomposition of some metal complexes of 5,5′-methylendisalicylhydroxamic acid

The thermal behaviour of the chelates of 5,5′-methylendisalicylhydroxamic acid with Pb(II), Zn(II), Ni(II), Cd(II), Fe(III), Cr(III), Al(III), Ti(IV), V(V), Mo(VI) and Cu(II) has been studied by thermogravimetry (TG), differential thermal analysis (DTA), IR spectroscopy and X-ray diffraction.The compounds decompose through three major steps, dehydration, transformation of the anhydrous hydroxamates to intermediate N-hydroxylactams, which decompose to yield metal oxides as the final products.     

Kinetics of thermal degradation in non-isothermal conditions of some phosphorus-containing polyesters and polyesterimides

The thermal decomposition behavior of some phosphorus-containing polyesters and a polyesterimide was studied using thermogravimetric analysis in air at several heating rates between 5 °C/min and 20 °C/min. The results of this study, realized for polymers with phosphorus linkage as pendant group, were compared with the behavior of some polymers having the same backbone structure, with phosphorus in the main chain, respectively, without phosphorus. The kinetic processing of data was carried out using the Coats-Redfern, Reich-Levi, Flynn-Wall-Ozawa and Kissinger methods.     

Stability constants of complexes of N-arylhydroxamic acids with some bivalent metal ions

Thermodynamic stability constants of complexes of Mn(II), Ni(II), Zn(II) and Cu(II) with five closely related N-arylhydroxamic acids have been determined at 25 +/- 0.1 degrees in 50% v v aqueous dioxan medium. The stabilities of the complexes mostly follow the order of the basicity of the ligands and the electron affinities of the metal ions as measured by their second ionization potential.