Authors:K. Gjurova, M. Michailov, B. Bogdanov, and C. Uzov
The thermal behaviour (from 20 to 500°C) of high-molecular polyoxyethylene-urea mixtures which formed a molecular complex
was investigated by means of a derivatograph. Under the conditions of the investigation, there were no indications of an interaction
between the thermal decomposition products and the initial components, or of new intermediates with a thermostabilizing effect.
A linear coorelation was obtained between the mass loss at 250°C and the urea content of the mixture, which may be used to
determine the urea content of similar mixtures.
Authors:G. Keller, F. Lavigne, C. Loisel, M. Ollivon, and C. Bourgaux
The thermal behavior of three ural fats (displaying very different composition), cocoa butter (CB)2, lard, and a stearin obtained from anhydrous milk-fat (AMF) fractionation, were studied by both DSC and X-ray diffraction as a function of temperature (XRDT). To perform temperature explorations between −30‡C and +80‡C, at rates identical to those used for DSC and ranging from 0.1 K min−1 to 10 K min−1, a new set of X-ray sample-holders, temperature-controlled by Peltier effect, has been developed. It is shown that the three more stable polymorphic forms of CB were easily characterized by either X-ray diffraction or DSC, and existence of two Β-3L forms was confirmed. On the contrary, the more complex polymorphism of lard and AMF required combined examination by DSC and XRDT and the brightness of the synchrotron source for studies at the highest heating rates. Quantitative analysis of the long spacings of XRDT recordings is invaluable for interpretation of thermal events. For instance, it was found that the simultaneous formation of two polymorphic forms, of apparent long spacing of 34 and 42 å, at the onset of lard crystallization might explain the difficulty of its fractionation.
Authors:J. Giusti, G. G. T. Guarini, L. Menabue, and G. C. Pellacani
The thermal behaviour of single-crystals of the title compound has been investigated by means of thermal methods supported by optical microscopy. A complex change takes place on heating. After the loss of the two water molecules, leading to an amorphous phase, recrystallization takes place. This results in a solid (probably an anhydrous form) which reacts further, through partial liquefaction, to yield a red crystalline product whose structure has been characterized via X-ray powder spectra and electronic and IR spectroscopy.
Authors:I. Pálinkó, I. Kiricsi, Gy. Tasi, and K. Varga
Natural montmorillonite was pillared by various polyhydroxy cations. The resulting pillared layer clays (PILCs) were characterized by X-ray fluorescence, X-ray diffraction (XRD) and infrared (IR) spectroscopies. The thermal behaviour of Al-PILC was investigated in detail by a combonation of XRD, derivatography IR spectroscopy and a comparison to natural montmorillonite is given. It was found that thermal stability of Al-PILC is lower than that of natural montmorillonite. However, heat treatment in the stability region results in significant sintering of natural montmorillonite, while the interlayer spacing of Al-PILC is hardly affected.
Authors:I. Pastre, I. do Nascimento Oliveira, A. Moitinho, G. de Souza, E. Ionashiro, and F. Fertonani
The composite montmorillonite-8-hydroxyquinoline (Swy-1-8-HQ) was prepared by two different processes and studied by using
thermogravimetric analysis (TG/DTG and DSC), as well as helpful techniques as fluorescence in the UV-visible region and X-ray
diffraction. The composites developed fluorescent appearance, however with quantum poor efficiency and they exhibited distinct
TG and DSC thermal behavior. The fluorescence data of spectra associated to the TG/DT curves allowed to suggest that the 8-HQ
was present in the composites in two different circumstances: 1 - intercalated in the interlayer spaces (Swy-1-8-HQ2), rigidly
associated to the substrate feasible as a monolayer with the aromatic rings parallel to the silica layer; and/or, 2 - adsorbed
on the surface (Swy-1-8-HQ1), either as a bilayer formation or tilting of the molecules to the silicate layer sheet. All results
confirmed above are in agreement with X-ray diffraction patterns, once the interlayer space increases when 8-HQ is incorporated.
The experimental results confirm the formation of the composites in agreement with the method used in the preparation.
The western region of the Deccan Volcanic Province (DVP) is constituted of tholeiitic lava flows. They host numerous cavities,
varying in size and shape, largely occupied by zeolites and a variety of secondary minerals, amongst which the fibrous zeolites
(natrolite group), are particularly gorgeous and attractive. Scolecite and mesolite are the only two members commonly occurring
in this region. Our data on their thermal behaviour significantly differs from that reported in previous literature. Scolecite,
Ca8(Al16Si24O80)·24H2O shows three distinct steps instead of two and water loss is observed even beyond 550°C. It is held that the first step corresponds
to the expulsion of water from the site farthest away from Ca and the next two steps in succession correspond to the two sites
nearer to Ca. Mesolite, Na16Ca16(Al48Si72O240)· 64H2O has much more complex behaviour with four or five steps of water expulsion and a major loss around 248–270°C in a double
reaction attributed here to the expulsion of water from scolecite type channels. It is further held that the natrolite type
channels are emptied in further steps. Loss of water in steps even beyond 400°C is particularly noted and such reactions are
well reflected in the TG and the DTG. Peak temperature dependence on sample amounts is also evident. Successive phase transformations
above 700°C, up to 1000°C are reflected in the DTA curves.
Authors:R. Marinkovic-Neducin, E. Kiss, T. Cukic, and D. Obadovic
The purified bentonite parent clay, fraction ≤; 2 mm of montmorillonite type, has been pillared by various polyhydroxy cations,
Al, AlFe and AlCu, using conventional pillaring methods. The thermal behavior of PILCs was investigated by combination of
X-ray diffraction (XRD), thermal analysis (DTA, TG) and low temperature N2 adsorption/desorption (LTNA). Thermal stability
of Al-, AlFe- and AlCu-PILC samples was estimated after isothermal pretreatment in static air on the temperatures 300, 500,
600 and 900C. Crucial structural changes were not registered up to 600C, but the fine changes in interlayer surrounding
and porous/microporous structure being obvious at lower temperatures, depending on the nature of the second pillaring ion.
AlFe-PILC showed higher thermal stability of the texture, the AlCu-PILC having lower values and lower thermal stability concerning
both overall texture and micropore surface and volume. Poorer thermal stability of AlCu-PILC sample at higher temperatures
was confirmed, the presence of Cu in the system contributing to complete destruction of aluminum silicate structure, by 'extracting'
aluminum in stabile spinel form.
The paper deals with the thermal behaviour of trimethoxy silane (MTS) modified ethyl methacrylate (EMA) and butyl methacrylate (BMA). Several copolymer samples were prepared by varying the molar ratio of MTS with respect to EMA or BMA. The copolymerisation was carried out at 78 °C for 120 min using benzoyl peroxide as an initiator. Incorporation of MTS in alkyl methacrylates resulted in an increase in thermal stability. Hydrolytic cross-linking of copolymer having higher mole fraction of MTS gave a cross-linked product with better thermal stability.
Authors:A. B. Garcia, E. R. Galán, J. A. S. Blázquez, and C. V. Calahorro
The thermal behaviour of some 2-benzylamino-2-deoxyheptonic acids obtained from 2-benzylamino-2-deoxy-D-glycero-L-gluco, 2-benzylamino-2-deoxy-D-glycero-D-ido and 2-benzylamino-2-deoxy-D-glycero-D-taloheptononitriles (reported) previously has been studied in air (static atmosphere) and N2 (dynamic atmosphere, flow rate 200 ml/min).
Thermal gravimetric (TG) and differential thermal (DTA) analyses were performed to characterize the thermal behavior and the
stoichiometry of uranyl bis-1,3-diketonate complexes (R1COCR2COR3)2 UO2x H2O, where R1,3=CH3; C2H5; C6H5; CF3; pNO2−C6H4; pCl−C6H4; pMe−C6H4; NH−C6H5; R2=H, C6H5 andx=1; 2. Based on the data obtained, a thermal degradation mechanism for each complex was proposed. The final degradation product
for all studied complexes was U3O8 oxide. The temperature of the first organic fragment rupture including the U-O (ligand) bond was taken as criterion for the
thermal stability of the metal-oxygen donor bond in these complexes. The observed stability order is in good agreement with
the IR determined constant force values,k, of the U-O (ligand) bond.