Kinetic study of the second stage of the dolomite thermal decomposition

2008 ◽  
Vol 33 (1) ◽  
pp. 47-57 ◽  
Author(s):  
Haykel Galai ◽  
Michèle Pijolat ◽  
Françoise Valdivieso ◽  
Kais Nahdi ◽  
Malika Trabelsi-Ayadi
2014 ◽  
Vol 69 (5) ◽  
Author(s):  
Nugroho Dewayanto ◽  
Ruzinah Isha ◽  
Mohd Ridzuan Nordin

The kinetic study on the catalytic pyrolysis of decanter cake (DC) from palm oil milling plant was carried out using thermogravimetry method. Catalysts were added to dry DC in desired ratio and then mixed manually. Based on the thermogravimetric analysis (TGA) results, the main thermal decomposition of both non-catalytic and catalytic pyrolysis of DC occurred at 210–530°C. Coats-Redfern method was used in this study. Two stage reactions were identified during the main thermal decomposition, with the first stage at 210–330°C, while second stage occurred at 330–530°C. The pyrolysis reaction obeyed the first and second order kinetic model for first and second stage reaction, respectively. The presence of the catalysts reduced the activation energy of thermal decomposition in both stages. Minimum activation energy value was observed at 10 wt% of catalyst loading.


2015 ◽  
Vol 106 ◽  
pp. 721-727 ◽  
Author(s):  
Chao Gai ◽  
Yuping Dong ◽  
Pengfei Fan ◽  
Zhaoling Zhang ◽  
Jingcui Liang ◽  
...  

Fuel ◽  
2009 ◽  
Vol 88 (6) ◽  
pp. 1024-1030 ◽  
Author(s):  
D.K. Shen ◽  
S. Gu ◽  
K.H. Luo ◽  
A.V. Bridgwater ◽  
M.X. Fang

2013 ◽  
Vol 49 (2) ◽  
pp. 275-283 ◽  
Author(s):  
André Luis Máximo Daneluti ◽  
Jivaldo do Rosário Matos

Phytic acid is a natural compound widely used as depigmenting agent in galenic cosmetic emulsions. However, we have observed experimentally that phytic acid, when heated to 150 ºC for around one hour, shows evidence of thermal decomposition. Few studies investigating this substance alone with regard to its stability are available in the literature. This fact prompted the present study to characterize this species and its thermal behavior using thermal analysis (TG/DTG and DSC) and to associate the results of these techniques with those obtained by elemental analysis (EA) and absorption spectroscopy in the infrared region. The TG/DTG and DSC curves allowed evaluation of the thermal behavior of the sample of phytic acid and enabled use of the non-isothermal thermogravimetric method to study the kinetics of the three main mass-loss events: dehydration I, dehydration II and thermal decomposition. The combination of infrared absorption spectroscopy and elemental analysis techniques allowed evaluation of the intermediate products of the thermal decomposition of phytic acid. The infrared spectra of samples taken during the heating process revealed a reduction in the intensity of the absorption band related to O-H stretching as a result of the dehydration process. Furthermore, elemental analysis results showed an increase in the carbon content and a decrease in the hydrogen content at temperatures of 95, 150, 263 and 380 °C. Visually, darkening of the material was observed at 150 °C, indicating that the thermal decomposition of the material started at this temperature. At a temperature of 380 °C, thermal decomposition progressed, leading to a decrease in carbon and hydrogen. The results of thermogravimetry coupled with those of elemental analysis allow us to conclude that there was agreement between the percentages of phytic acid found in aqueous solution. The kinetic study by the non-isothermal thermogravimetric method showed that the dehydration process occurred in two stages. Dehydration step I promoted a process of vaporization of water (reaction order of zero), whereas dehydration step II showed an order of reaction equal to five. This change in reaction order was attributed to loss of chemically bonded water molecules of phytic acid or to the presence of volatile substances. Finally, the thermal decomposition step revealed an order of reaction equal to one. It was not possible to perform the kinetic study for other stages of mass loss.


2016 ◽  
Vol 13 (2) ◽  
pp. 505-525 ◽  
Author(s):  
Mohsen Ravanbod ◽  
Hamid Pouretedal ◽  
Mohammad Amini ◽  
Reza Ebadpour

2015 ◽  
Vol 30 (5) ◽  
pp. 691-706 ◽  
Author(s):  
Xinghua Guan ◽  
Xiaoyan Ma ◽  
Hualong Zhou ◽  
Fang Chen ◽  
Zhiguang Li

Two diblock copolymers of poly(methyl methacrylate)- block-poly(styrene) with chlorine as terminal group (PMMA- b-PS-Cl) were synthesized via two-step atom transfer radical polymerization. The structures of the block copolymers were characterized by Fourier transform infrared spectroscopy, proton nuclear magnetic resonance, and gel permeation chromatography. Thermal properties including glass transition temperature ( Tg) and thermal stability were studied by differential scanning calorimetry and thermogravimetric analysis (TGA), respectively. The block copolymers of PMMA- b-PS-Cl exhibited two glass transitions, which were attributed to the Tgs of PMMA and PS segments, respectively. According to TGA, thermal decompositions of PMMA macro-initiator and PMMA- b-PS-Cl block copolymers had two stages. The weight loss ratio in the second stage was more significant than that in the first stage, which may be attributed to the separation of the halogen atom from the terminal group and the formation of a double bond. The breaking down of the backbone dominates in the second stage in which the weight loss ratio was more than 70%, represented the main stage of pyrolysis. It was found that the introduction of the PS chain remarkably enhanced the thermal stability of the copolymer, thus endowing the block copolymers high activation energy for thermal decomposition. On the other hand, the remaining two pyrolysis procedures further indicated that thermodynamic mechanism didn’t change due to the introduction of PS segments.


2017 ◽  
Vol 5 (5) ◽  
pp. 4858-4865 ◽  
Author(s):  
Alexandru C. Sonoc ◽  
Chris Thurgood ◽  
Brant Peppley ◽  
David G. Kelly

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