scholarly journals Non-Isothermal Decomposition of 2-(2-Hydroxybenzylideneamino)-3-phenylpropanoic Acid in Nitrogen Atmosphere

2011 ◽  
Vol 8 (2) ◽  
pp. 819-829
Author(s):  
M. Vennila ◽  
G. Manikandan ◽  
V. Thanikachalam ◽  
J. Jayabharathi

The non-isothermal decomposition properties of 2-(2-hydroxy- benzylideneamino)-3-phenylpropanoic acid [HBAPPA] have been studied using microanalysis, FT-IR, UV, DTA, DTG and TG techniques. The TG studies were carried out at different heating rates of 10, 15 and 20 K/min. The Schiff base decomposed in three stages. The kinetic parameters were deduced for each stage. A probable mechanism has been proposed for the decomposition process.

2019 ◽  
Vol 10 (1) ◽  
pp. 72-81
Author(s):  
Ganesan Nalini ◽  
Natesan Jayachandramani ◽  
Radhakrishnan Suresh ◽  
Prakasam Thirumurugan ◽  
Venugopal Thanikachalam ◽  
...  

A new compound, spiro-oxindole derivative compound namely ethyl-2ʹ-amino-5ʹ-cyano-6ʹ-(1H-indole-3yl)-2-oxospiro[indoline-3,4ʹ-pyran]-3ʹ-carboxylate (EACIOIPC) has been synthesized and characterized by microanalysis, FT-IR, mass spectrum and NMR (1H and 13C) techniques. The thermal decomposition of the compound was studied by thermogravimetric analysis under dynamic nitrogen atmosphere at different heating rates of 10, 15, 20 and 30 K/min. The kinetic parameters were calculated using model-free (Friedman’s, Kissinger-Akahira-Sunose (KAS) and Flynn-Wall-Ozawa (FWO) methods) and model-fitting (Coats and Redfern (CR)) methods. The decomposition process of EACIOIPC followed a single step mechanism as evidenced from the data. Existence of compensation effect is noticed for the decomposition of EACIOIPC. Invariant kinetic parameters are consistent with the average values obtained by Friedman and KAS in conversional methods.


2018 ◽  
Vol 72 (2) ◽  
pp. 99-106 ◽  
Author(s):  
Milos Radojevic ◽  
Martina Balac ◽  
Vladimir Jovanovic ◽  
Dragoslava Stojiljkovic ◽  
Nebojsa Manic

In the Republic of Serbia there are significant quantities of coffee and tire wastes that can be utilized as Solid Recovered Fuel (SRF) and used as an additional fuel for co?combustion with coal and biomass in energy production and cement industry sectors. Differences between SRF and base fuel are a cause of numerous problems in design of burners. The objective of this study was to determine the kinetic parameters for the thermochemical conversion of selected SRF using Simultaneous Thermal Analysis (STA). Samples of coffee and tire waste were used for the experimental tests. Thermal analysis was carried out in nitrogen atmosphere at three different heating rates 10, 15 and 20 K/min for each sample, while it was heated from room temperature up to 900?C. Two sample sizes x <0.25 mm and 0.25 < x <0.5 mm of each SRF were used in experiments, in order to obtain reliable Thermal Gravimetric Analysis (TGA) data for estimation of kinetic parameters for SRF pyrolysis. Experimental results were used for determination of pre-exponential factor and activation energy according to methods presented in the literature. Presented research provides valuable data of coffee and tire waste that can be used for the burners design.


2018 ◽  
Vol 39 (1) ◽  
pp. 58-67 ◽  
Author(s):  
Dev K. Mandal ◽  
Haripada Bhunia ◽  
Pramod K. Bajpai

AbstractIn this article, the influence of polylactide and pro-oxidant on the thermal stability, degradation kinetics, and lifetime of polypropylene has been investigated using thermogravimetric analysis under nitrogen atmosphere at four different heating rates (i.e. 5, 10, 15, and 20°C/min). The kinetic parameters of degradation were studied over a temperature range of 30–550°C. The derivative thermogravimetric curves have indicated single stage and two stage degradation processes. The activation energy was evaluated by using the Kissinger, Kim-Park, and Flynn-Wall methods under the nitrogen atmosphere. The activation energy value of polypropylene was much higher than that of polylactide. Addition of polylactide and pro-oxidant in polypropylene decreased the activation energy. The lifetime of polypropylene has also decreased with the addition of polylactide and pro-oxidant.


2011 ◽  
Vol 110-116 ◽  
pp. 155-162 ◽  
Author(s):  
W. M. Abdel-Wareth ◽  
Xu Xu

Effects of various grain sizes (10~390 µm) under heating rate of 40 °C/min on ammonium perchlorate (AP) decomposition characteristic parameters, the decomposition thermal behavior and kinetic parameters (activation energy and pre-exponential factor), were investigated by simultaneous DSC/TGA in a dynamic nitrogen atmosphere. In addition, the specific surface areas were measured by the BET-method. Moreover, the kinetic parameters were determined by a simplified approach based on the isoconversional method. The results showed that, the higher the AP particle size the lower the determined decomposition kinetic parameters. In addition, the results were in acceptable agreements with some important literatures. Moreover, it was highly recommended to apply the higher agreeable heating rates for AP samples to determine that parameters more accurately.


1996 ◽  
Vol 50 (8) ◽  
pp. 1058-1065 ◽  
Author(s):  
Leo C. K. Liau ◽  
Thomas C. K. Yang ◽  
Dabir S. Viswanath

Poly(vinyl butyral) (PVB) was thermally degraded in a thermogravimetry (TG) in nitrogen atmosphere. Evolving gases during PVB degradation were continuously analyzed with an FT-IR instrument. The main products identified were butyraldehyde, 2-butenal, butanoic acid, acetic acid, 2,5-dihydrofuran, and butanol. The IR spectra of mixture gases were resolved on the basis of the spectrum of pure species. The intensity of IR absorbance for each species was recorded as a function of temperature, and the temperature-dependent quantitative information for each species was calculated and used to evaluate the kinetic parameters. Activation energy and preexponential factors were evaluated for each species under the assumption of a parallel degradation mechanism and first-order kinetics. In addition to this detailed analysis, the polymer weight loss information measured by TG was used to determine the overall kinetic parameters. Results showed that activation energy obtained by both methods was consistent.


2010 ◽  
Vol 64 (2) ◽  
Author(s):  
Lukáš Gašparovič ◽  
Zuzana Koreňová ◽  
Ľudovít Jelemenský

AbstractPyrolysis of a wood chips mixture and main wood compounds such as hemicellulose, cellulose and lignin was investigated by thermogravimetry. The investigation was carried out in inert nitrogen atmosphere with temperatures ranging from 20°C to 900°C for four heating rates: 2 K min−1, 5 K min−1, 10 K min−1, and 15 K min−1. Hemicellulose, cellulose, and lignin were used as the main compounds of biomass. TGA and DTG temperature dependencies were evaluated. Decomposition processes proceed in three main stages: water evaporation, and active and passive pyrolysis. The decomposition of hemicellulose and cellulose takes place in the temperature range of 200–380°C and 250–380°C, while lignin decomposition seems to be ranging from 180°C up to 900°C. The isoconversional method was used to determine kinetic parameters such as activation energy and pre-exponential factor mainly in the stage of active pyrolysis and partially in the passive stage. It was found that, at the end of the decomposition process, the value of activation energy decreases. Reaction order does not have a significant influence on the process because of the high value of the pre-exponential factor. Obtained kinetic parameters were used to calculate simulated decompositions at different heating rates. Experimental data compared with the simulation ones were in good accordance at all heating rates. From the pyrolysis of hemicellulose, cellulose, and lignin it is clear that the decomposition process of wood is dependent on the composition and concentration of the main compounds.


1988 ◽  
Vol 42 (4) ◽  
pp. 655-658 ◽  
Author(s):  
Randy W. Snyder ◽  
C. Wade Sheen

A method is shown for the determination of kinetic parameters from dynamic FT-IR experiments. The effect heating rate has on the reproducibility of the calculated activation energy is discussed. The curing of PMDA/ODA polyimide at several heating rates is given as an example.


2012 ◽  
Vol 178-181 ◽  
pp. 1093-1096
Author(s):  
Quan Cheng Zhou ◽  
Gui Hua Sheng

The pyrolytic characteristics and kinetics of Xanthoceras sorbifolia oil were investigated pyrolysis in indifferent atmosphere and at heating rates of 10, 20 and 30 °C min-1 in an inert atmosphere. The most probable mechanism function and activation energy pre-exponential factors were calculated by the Popescu, FWO and KAS methods. Three stages appeared during pyrolysis: moisture evaporation, primary devolatilization and residual decomposition. Significant differences in the average activation energy, thermal stability, final residuals and reaction rates of the X. sorbifolia oil were observed. Stage II of the X. sorbifolia oil could be described by the Avramic- Erofeev equation 20 (n=4). The average activation energy of X. sorbifolia oil was 353 kJ mol-1


2020 ◽  
Vol 18 (1) ◽  
pp. 1304-1315
Author(s):  
Naushad Ahmad ◽  
Manawwer Alam ◽  
Rizwan Wahab ◽  
Mukhtar Ahmed ◽  
Ashfaq Ahmad

AbstractSchiff-base ligand, 2,6-bis(benzimino)-4-phenyl-1,3,5-triazine (L), and its transition metal complexes of Co(ii), Ni(ii), and Cu(ii) were synthesized by refluxing the reaction mixture and its analytical, spectral, and thermogravimetric characteristics were explored by various techniques: AAS, FT-IR, UV-vis, TG-DTG, CHNS/O, and VSM. It was observed that all the metal containing complexes are non-electrolytic, mononuclear, and paramagnetic in nature, confirmed by the molar conductance and magnetic susceptibility measurements. Optical spectral data were used to investigate the geometrical and spectral parameters of [Co(L)(ac)2], [Ni(L)(ac)2], [Cu(L)(ac)2], [Cu(L)(acac)2], and [Cu(L)(fmc)2] complexes. Simultaneous thermal analyses (TG-DTG) in nitrogen atmosphere reveal that the ligand decomposes in one step, [Co(L)(ac)2], [Ni(L)(ac)2], and [Cu(L) (ac)2] complexes are decomposed in three steps, whereas [Cu(L)(acac)2] and [Cu(L) (fmc)2] are decomposed in five and two steps, respectively. In addition, activation energy (Ea) and pre-exponential factor (ln A) were evaluated by TG-DTG decomposition steps of compounds using the Coats–Redfern formula. Enthalpy (∆H), entropy (∆S), and Gibbs free energy (∆G) of the as-prepared metal complexes were also speculated by various thermodynamic equations.


2017 ◽  
Vol 68 (8) ◽  
pp. 1895-1902
Author(s):  
Ioana Cristina Tita ◽  
Eleonora Marian ◽  
Bogdan Tita ◽  
Claudia Crina Toma ◽  
Laura Vicas

Thermal analysis is one of the most frequently used instrumental techniques in the pharmaceutical research, for the thermal characterization of different materials from solids to semi-solids, which are of pharmaceutical relevance. In this paper, simultaneous thermogravimetry/derivative thermogravimetry (TG/DTG) and differential scanning calorimetry (DSC) were used for characterization of the thermal behaviour of candesartan cilexetil � active substance (C-AS) under dynamic nitrogen atmosphere and nonisothermal conditions, in comparison with pharmaceutical product containing the corresponding active substance. It was observed that the commercial samples showed a different thermal profile than the standard sample, caused by the presence of excipients in the pharmaceutical product and to possible interaction of these with the active substance. The Fourier transformed infrared spectroscopy (FT-IR) and X-ray powder diffraction (XRPD) were used as complementary techniques adequately implement and assist in interpretation of the thermal results. The main conclusion of this comparative study was that the TG/DTG and DSC curves, together with the FT-IR spectra, respectively X-ray difractograms constitute believe data for the discrimination between the pure substance and pharmaceutical forms.


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