PS-TiO2 Nanocomposites: Thermal Investigations

2011 ◽  
Vol 1312 ◽  
Author(s):  
Rafael Villegas ◽  
Yun Zhai ◽  
Hailan Xu ◽  
Dorina Magdalena Chipara ◽  
David Hui ◽  
...  

ABSTRACTNanocomposites of polystyrene loaded with various amounts of anatase (ranging between 0 % wt. and 20 % wt.) have been synthesized and investigated by thermal analysis. The research was focused on the simulation of Thermogravimetric Analysis data, aiming to a refined understanding of the interactions between of polystyrene and TiO2 nanoparticles. The dependence of the first derivative of residual mass on temperature has been used to determine more accurately the temperature at which the mass loss is maxim. Several functions have been used to simulate the dependence of the first derivative of mass loss on the temperature of the sample. The highest correlation coefficient was obtained for the asymmetric Gaussian combination, which connects two halves of a Gaussian line with different linewidth. An increase of the thermal stability of the polymeric matrix upon loading with TiO2 is reported.

1972 ◽  
Vol 50 (23) ◽  
pp. 3872-3875 ◽  
Author(s):  
Kim Vo Van ◽  
Fathi Habashi

Anhydrous CU2SO4 was prepared and its X-ray diffraction pattern was established. Differential thermal analysis, thermogravimetric analysis, and X-ray diffraction methods were used to study the effect of heating in different atmospheres. The formation of CU2SO4 as an intermediate in chemical processes has been discussed.


2019 ◽  
Author(s):  
Andreas Boelke ◽  
Yulia A. Vlasenko ◽  
Mekhman S. Yusubov ◽  
Boris Nachtsheim ◽  
Pavel Postnikov

<p>The thermal stability of pseudocyclic and cyclic <i>N</i>-heterocycle-stabilized (hydroxy)aryl- and mesityl(aryl)-l<sup>3</sup>-iodanes (NHIs) through thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) is investigated. NHIs bearing <i>N</i>-heterocycles with a high N/C-ratio such as triazoles show among the lowest descomposition temperatures and the highest decomposition energies. A comparison of NHIs with known (pseudo)cyclic benziodoxolones is made and we further correlated their thermal stability with reactivity in a model oxygenation. </p>


Calphad ◽  
2021 ◽  
Vol 73 ◽  
pp. 102258
Author(s):  
František Zelenka ◽  
Jakub Strádal ◽  
Pavel Brož ◽  
Jan Vřešťál ◽  
Jiří Buršík ◽  
...  

2007 ◽  
Vol 79 (11) ◽  
pp. 1879-1884 ◽  
Author(s):  
Smaranda Iliescu ◽  
Gheorghe Ilia ◽  
Aurelia Pascariu ◽  
Adriana Popa ◽  
Nicoleta Plesu

Direct, efficient, organic solvent- and catalyst-free synthesis of a series of polyphosphates was accomplished. The reaction involved a gas-liquid interfacial polycondensation between arylphosphoric dichlorides and bisphenol A. The polyphosphates were characterized by IR, 1H NMR, 31P NMR, inherent viscosity, thermal analysis, and molar mass. Yields in the range 70-90 % and inherent viscosities in the range 0.30-0.40 dl/g were obtained. The thermal stability of the polyphosphates was investigated by using thermogravimetry.


2021 ◽  
Vol 875 ◽  
pp. 116-120
Author(s):  
Muhammad Alamgir ◽  
Faizan Ali Ghauri ◽  
Waheed Qamar Khan ◽  
Sajawal Rasheed ◽  
Muhammad Sarfraz Nawaz ◽  
...  

In this study, the effect of SBR concentration (10 Phr, 20 Phr & 30 Phr ) on the thermal behavior of EPDM/SBR blends was studied. Thermogravimetric analysis (TGA) was used to check weight loss of samples as function of temperature by heating upto 600°C. X-ray diffraction (XRD) was performed to determine quality and % crystallinity of the elastomer blends. It was seen that % crystallinity improved with an increase in the content of SBR in EPDM/SBR blends. TGA revealed that the thermal stability of EPDM/SBR blends has improved by 17% than neat EPDM. Carbon nano-coatings produced by sputtering have no beneficial influence on thermal behaviour of elastomers.


2018 ◽  
Vol 39 (4) ◽  
pp. 21
Author(s):  
Gilbert Bannach ◽  
Rafael R. Almeida ◽  
Luis G. Lacerda ◽  
Egon Schnitzler ◽  
Massao Ionashiro

Several papers have been described on the thermal stability of the sweetener, C12H19Cl3O8 (Sucralose). Nevertheless no study using thermoanalytical techniques was found in the literature. Simultaneous thermogravimetry and differential thermal analysis (TG-DTA), differential scanning calorimetry (DSC) and infrared spectroscopy, have been used to study the thermal stability and thermal decomposition of sweetener.


2018 ◽  
Vol 19 (12) ◽  
pp. 3723 ◽  
Author(s):  
Shaoyun Chen ◽  
Min Xiao ◽  
Luyi Sun ◽  
Yuezhong Meng

The terpolymerization of carbon dioxide (CO2), propylene oxide (PO), and cyclohexene oxide (CHO) were performed by both random polymerization and block polymerization to synthesize the random poly (propylene cyclohexene carbonate) (PPCHC), di-block polymers of poly (propylene carbonate–cyclohexyl carbonate) (PPC-PCHC), and tri-block polymers of poly (cyclohexyl carbonate–propylene carbonate–cyclohexyl carbonate) (PCHC-PPC-PCHC). The kinetics of the thermal degradation of the terpolymers was investigated by the multiple heating rate method (Kissinger-Akahira-Sunose (KAS) method), the single heating rate method (Coats-Redfern method), and the Isoconversional kinetic analysis method proposed by Vyazovkin with the data from thermogravimetric analysis under dynamic conditions. The values of ln k vs. T−1 for the thermal decomposition of four polymers demonstrate the thermal stability of PPC and PPC-PCHC are poorer than PPCHC and PCHC-PPC-PCHC. In addition, for PPCHC and PCHC-PPC-PCHC, there is an intersection between the two rate constant lines, which means that, for thermal stability of PPCHC, it is more stable than PCHC-PPC-PCHC at the temperature less than 309 °C and less stable when the decomposed temperature is more than 309 °C. Pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and thermogravimetric analysis/infrared spectrometry (TG/FTIR) techniques were applied to investigate the thermal degradation behavior of the polymers. The results showed that unzipping was the main degradation mechanism of all polymers so the final pyrolysates were cyclic propylene carbonate and cyclic cyclohexene carbonate. For the block copolymers, the main chain scission reaction first occurs at PC-PC linkages initiating an unzipping reaction of PPC chain and then, at CHC–CHC linkages, initiating an unzipping reaction of the PCHC chain. That is why the T−5% of di-block and tri-block polymers were not much higher than that of PPC while two maximum decomposition temperatures were observed for both the block copolymer and the second one were much higher than that of PPC. For PPCHC, the random arranged bulky cyclohexane groups in the polymer chain can effectively suppress the backbiting process and retard the unzipping reaction. Thus, it exhibited much higher T−5% than that of PPC and block copolymers.


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