scholarly journals OPTIMIZING THE WELDING OF PLASTICS WITH THE USE OF DIFFERENTIAL SCANNING CALORIMETRY AND THERMOGRAVIMETRIC ANALYSIS

2014 ◽  
Vol 54 (3) ◽  
pp. 221-224 ◽  
Author(s):  
Michal Ondruška ◽  
Marián Drienovský ◽  
Roman Čička ◽  
Milan Marônek ◽  
Antonín Náplava

Plastics have different thermal stability, depending on the structure of the polymer chains. It is therefore very important to know their thermal properties, which influence the temperature regime of processing equipment. This paper presents examples of differential scanning analysis (DSC) and thermogravimetry analysis (TG) of selected plastics in an Ar protective atmosphere and also in an oxidative atmosphere of static air. These analyses can be used for proposing a welding temperature regime.

Materials ◽  
2019 ◽  
Vol 12 (16) ◽  
pp. 2636
Author(s):  
Tomasz M. Majka ◽  
Oskar Bartyzel ◽  
Konstantinos N. Raftopoulos ◽  
Joanna Pagacz ◽  
Krzysztof Pielichowski

Pyrolysis of the polypropylene/montmorillonite (PP/OMMT) nanocomposites allows for recovery of the filler that can be then re–used to produce PP/pyrolyzed MMT (PMMT) nanostructured composites. In this work, we discuss the thermal properties of PP/PMMT composites investigated by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). It has been found that effect of PMMT (5 wt. % and 10 wt. %) on matrix thermal stability occurs at temperatures above 300 °C. Addition of 5 wt. % and 10 wt. % of PMMT into polypropylene system gave good stabilization effect, as confirmed by the overall stabilization effect (OSE) values, which increased by 4% and 7%, respectively, compared to the control sample (PP). Interestingly, the presence of 1 wt. % and 3 wt. % of pyrolyzed clay stabilizes the system better than the same concentrations of organoclay added into polypropylene melt. DSC data revealed that pyrolyzed clay has still the same tendency as organoclay to enhance formation of the α and β crystalline PP phases only. The pyrolyzed MMT causes an improvement of the modulus in the glassy as well as rubbery regions, as confirmed by DMA results.


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>


2021 ◽  
Vol 287 ◽  
pp. 02014
Author(s):  
Amin Abbasi ◽  
Mohamed Mahmoud Nasef ◽  
Wan Zaireen Nisa Yahya ◽  
Muhammad Moniruzzaman

The conversion of palm oil into a sulfur-based polymer by copolymerization with sulfur powder at its molten state is herein reported. The obtained sulfur-containing polymer was characterized using Fourier transform infrared (FTIR), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC) to demonstrate the successful conversion. The disappearance of the peaks related to vinylic groups of oil together with the appearance of a peak representing C-H rocking vibrations in the vicinity of C-S bonds confirmed the copolymerization of sulfur with oil. TGA revealed that the polymers have thermal stability up to 230°C under nitrogen and the polymers leave 10% sulfur-rich ash. DSC proved that a small amount of elemental sulfur remained unreacted in the polymer, which showed amorphous and heavily crosslinked structure resembling thermosets. These copolymers are an environmental-friendly polymeric material promoting the utilization of the abundant sulfur while also adding value to palm oil.


2020 ◽  
Vol 20 (8) ◽  
pp. 4657-4660
Author(s):  
Kyeong Hyeon Kim ◽  
Jae Hyeok Lee ◽  
Dong-Eun Kim ◽  
Hoon-Kyu Shin ◽  
Burm-Jong Lee

An isomeric series of phosphine oxides with N-phenyl benzimidazole such as 2-DPPI, 3-DPPI and 4-DPPI were synthesized for organic light emitting diodes (OLED). The thermal properties of DPPI isomers were determined by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). OLED devices using DPPI isomers as the emitting material were fabricated, which configuration was ITO/MoOx [30 nm]/NPB [500 nm]/DPPI [300 nm]/Alq3 [200 nm]/Liq[10 nm]/Al [120 nm]. The emitting colors of the devices were respectively a deep-blue (430 nm, 4-DPPI) and greenish-yellows (510–580 nm, 3-DPPI and 530 nm, 2-DPPI). In particular, the emitting color of 4-DPPI device was not changed during the alteration of applied voltages (6.5–11.5 V), and the CIE coordinate was a satisfactory deep-blue (0.161, 0.101).


2016 ◽  
Vol 29 (10) ◽  
pp. 1139-1147 ◽  
Author(s):  
Zi Sang ◽  
Tiantian Feng ◽  
Wenbin Liu ◽  
Jun Wang ◽  
Mehdi Derradji

A new series of aniline and aniline-mixed tetrafunctional fluorene-based oxazine monomers were synthesized using 2,7-hydroxy-9,9-bis-(4-hydroxyphenyl) fluorene, paraformaldehyde, and primary amines (including aniline or aniline mixed with n-butylamine or n-octylamine composition). Fourier transform infrared spectroscopy and proton nuclear magnetic resonance spectroscopy were used to characterize the structure of the monomers. The copolymers were obtained by adding the monomers into a typical monofunctional polybenzoxazine (phenol-aniline-based benzoxazine). Differential scanning calorimetry, thermogravimetric analysis, and dynamic mechanical analysis were performed to study the thermal properties of the copolymers. The copolymers exhibited high glass transition temperature values (164–201°C). A good thermal stability was also obtained with a 5% weight loss temperature over 355°C and high char yields at 800°C (42–50%).


1992 ◽  
Vol 4 (2) ◽  
pp. 67-71
Author(s):  
N. R. Patel ◽  
N. Z. Patel ◽  
R. M. Patel

Unsaturated polyamides were prepared by condensing /3(4-ethoxyphenyl) glutaconic acid with various aromatic diamines. The polycondensates were characterized by IR spectroscopy, vapor phase osmometry, thermogravimetric analysis, differential scanning calorimetry and elemental analysis. All resins were found to decompose in the range '-210-600 °C. The kinetics of decomposition were studied. The results indicated that the resins possess reasonably good thermal stability.


BioResources ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. 3171-3185
Author(s):  
Perry Law Nyuk Khui ◽  
Rezaur Rahman ◽  
Abu Saleh Ahmed ◽  
Kuok King Kuok ◽  
Muhammad Khusairy Bin Bakri ◽  
...  

The morphological and thermal properties of composites containing a bioplastic blend and micro/nano-sized biochar from pyrolyzed jatropha seeds from microwave pyrolyzed jatropha seeds were investigated using scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, and differential scanning calorimetry. The biocomposite samples exhibited a brittle structure with a slightly ductile chip-like appearance. The Fourier transform infrared spectroscopy results for the PLA/PEMA/BC bio-composites were comparable to the PLA/BC biocomposites. A lower bio-filler content had more pronounced peak intensities than the higher bio-filler content biocomposites. The added PEMA compatibilizer in the PLA/PEMA/BC biocomposite showed more pronounced peaks, which indicated slightly improved bonding/interaction between the bio-filler and the matrix. Overall, increasing bio-filler content did not drastically affect the functional groups of the biocomposites. Thermogravimetric and differential scanning calorimetry analysis showed the developed biocomposites had a slight improvement in thermal stability, in comparison to the PLA sample. Improvements in the thermal stability of the PLA/PEMA/BC biocomposite could be attributed to the additional hydroxyl group, which was due to the added PEMA in the PLA and PLA/BC. According to the results of the analysis of the developed biocomposites, the biocomposites were more brittle and had reasonable thermal stability.


2019 ◽  
Vol 15 ◽  
pp. 2311-2318 ◽  
Author(s):  
Andreas Boelke ◽  
Yulia A Vlasenko ◽  
Mekhman S Yusubov ◽  
Boris J Nachtsheim ◽  
Pavel S Postnikov

The thermal stability of pseudocyclic and cyclic N-heterocycle-stabilized (hydroxy)aryl- and mesityl(aryl)-λ3-iodanes (NHIs) through thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) is investigated. Peak decomposition temperatures (T peak) were observed within a wide range between 120 and 270 °C. Decomposition enthalpies (ΔH dec) varied from −29.81 to 141.13 kJ/mol. A direct comparison between pseudocyclic and cyclic NHIs revealed high T peak but also higher ΔH dec values for the latter ones. NHIs bearing N-heterocycles with a high N/C-ratio such as triazoles show among the lowest T peak and the highest ΔH dec values. A comparison of NHIs with known (pseudo)cyclic benziodoxolones is made and we further correlated their thermal stability with reactivity in a model oxygenation.


Sign in / Sign up

Export Citation Format

Share Document