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The thermal decompositions ofβ-AlF3 · 3H2O, AlF3 · 3.5H2O, AlF3 · 1.5H2O,β-AlF3 and hydroxyfluorides of aluminium were investigated. The literature data were complemented with X-ray results. The first stages of decomposition are described. The AlF3 hydrates and hydroxyfluorides were used as model systems in order to interpret the thermal behaviour of α-AlF3 in more detail.

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The thermal stabilities of PVC/poly(MMA-co-DVB) polymer systems and membranes prepared by the paste method were investigated. The thermoanalytical curves were used to determine the main thermal stage of the decompositions. It was found that the thermal properties of the polymer systems were affected by the divinylbenzene content. A membrane based on the PVC/poly(MMA-co-DVB) system with 5 mass% DVB displays thermal stability up to 210C.

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The preparation of a new acid lanthanide diphosphate is reported. The acid praseodymium diphosphate, obtained as a trihydrate salt, is investigated by chemical analysis, X-ray powder diffraction and IR spectroscopy. The study of the thermal behavior of HPrP2O7·3H2O shows that its dehydration begins at 367 K. A scheme of its decomposition is proposed.

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Infrared spectra of a series of anhydrous (Rb, Cs) and hydrated (Na, K, Ca, Sr, Ba, Pb, Ag, Tl) salts of the complex anion VO(C3H2O4)2]2− were recorded and briefly discussed. The thermal behaviour of these compounds, as well as that of the corresponding diprotonated ethylenediamine cation, were investigated by TG- and DTA-methods in N2-atmosphere and complemented with studies carried out in crucible furnaces in air. Pyrolysis intermediates and residues were characterized by IR spectroscopy and overall stoichiometries for the degradation processes were proposed. In most cases orthovanadate/VO2 mixtures were obtained as final residues in N2, whereas the corresponding divanadates were produced in air.

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The thermal behaviour of a series of Ni-P alloys obtained by electroless plating from chloride-glycollate solutions at different pH values was studied by means of DSC analysis and X-ray diffraction.

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The thermal behaviour of [CoCO3(NH3)4]2SO4 · 3H2O was studied using X-ray diffraction diagrams, DTA, TG and heating at constant temperatures for different periods of time. The X-ray study was made in order to characterize with the powder diagrams the phases obtained and to follow the reactions of the complex when heated in air up to 800‡. A parallel infrared spectral study was also made. The results obtained by the various experimental methods were compared with the theoretical weight losses.

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Journal of Thermal Analysis and Calorimetry
Authors: Corina Duda-Seiman, T. Vlase, Gabriela Vlase, Rodica Cinca, Mariana Anghel, and N. Doca

screening drug-excipient interactions. The use of hyphenated techniques allows the identification of evolved volatile compounds resulted by thermodegradation process and an accurate determination of the differences in drug’s thermal behavior induced by

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The thermal behaviour ofγ-sulfur, monoclinicα-Se, S6Se2, S5Se3, S4Se4 and S3Se5, has been studied by hot-stage microscopy and differential scanning calorimetry. X-ray diffraction results show that S6Se2 and S5Se3 are isostructural with Sγ, but S4Se4 and S3Se5 are isostructural with monoclinicα-Se. The melting of Sγ, is accompanied by rapid crystallization of Sβ, which often occurs almost simultaneously with melting. The melting of S6Se2, S5Se3, S4S4 and S3Se5 is irreversible as the compounds decompose on melting. For monoclinicα-Se no phase transformation to monoclinicβ Se was observed at 110–120°, but it changes to hexagonalα-Se when the temperature is over 120°.

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Journal of Thermal Analysis and Calorimetry
Authors: Liang Xue, Feng-Qi Zhao, Xiao-Ling Xing, Zhi-Ming Zhou, Kai Wang, Hong-Xu Gao, Jian-Hua Yi, and Rong-Zu Hu

thermodynamic of 3,4,5-triamino-1,2,4-triazole dinitramide is a basic task in the content of thermal process. The thermal behavior of materials may be determined in a short time using thermal analysis techniques such as DSC, TG-DTG, but more intensive and

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The optimum conditions for extraction of ion-associated complexes (IAC) formed from the tetrazolium salt-tetrazolium violet and Sb(V) in hydrochloric acid medium have been studied. An isotope of antimony (125Sb) was used for determination of the recovery factor (R%) and distribution ratio (DSb). The thermal behavior of the antimony complex with tetrazole violet was studied using differential thermal and thermogravimetric analysis.

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