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of the synthesized copolymer was determined by TG. Figure 1 illustrates a comparison of the thermal degradation characteristics of synthesized copolymers with different molecular weights. Fig. 1

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process, such as activation energies ( E ) and reaction orders ( n ), etc. [ 5 – 10 ]. Kinetic data could help us to understand the thermal degradation mechanism [ 11 ]. In this article, the thermal degradation of BO6 has been investigated with TG

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Journal of Thermal Analysis and Calorimetry
Authors:
M. I. Loría-Bastarrachea
,
W. Herrera-Kao
,
J. V. Cauich-Rodríguez
,
J. M. Cervantes-Uc
,
H. Vázquez-Torres
, and
A. Ávila-Ortega

out that the formation of pyrrolidone is the main product of the thermal degradation of PVP. In contrast, Bianco et al. [ 3 ] suggested that the main volatile products of the thermal degradation of PVP are compounds with ester groups, ammonia (NH 3

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Journal of Thermal Analysis and Calorimetry
Authors:
Vadim V. Krongauz
,
Yann-Per Lee
, and
Anthony Bourassa

on the temperature and varied from 2 to 10 h. The TG of PVC degradation was conducted in air flow of 90 mL min −1 .The initial rate of thermal degradation was measured as a slope of the short-time linear portion of the kinetic curves of % mass loss

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transformation. From the analysis of the experimental results of a thermal degradation, one can construct a reaction kinetic model of the chemical processes leading from the precursor(s) to the product(s) of a reaction [ 1 ]. One well-known ligand—oxalate can be

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mass sample, m t is mass sample at t time during thermal degradation, and m f is the final mass when experiment finished. Taking into account that temperature is a function of time and increases with constant heating rate β the following

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thermal degradation in air (30–900 °C) to be specific and complex showing two domains as a function of temperature (time): an endothermic one which is identical to that for the degradation in nitrogen atmosphere and an exothermic one that cannot be found

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Introduction The phenomenon of synergism on thermal degradation was a focus today. Many researchers have investigated the effect of additives on thermal decomposition. Nie et al. [ 1 ] investigated the synergistic effect of the

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fiber and [ 8 , 9 ]. PBO shows a heat resistance about 100 °C higher than PPTA (Poly( p -phenylene terephthalamide) and there have been some reports about thermal analysis of PBO fibers [ 10 , 11 ]. The thermal degradation of PBZT and PBZO was studied

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attention due to its basic position in this group of material [ 4 – 8 ]. It is well known that thermal degradation of PDMS in inert atmosphere results in depolymerization at 400–650 °C to produce cyclic oligomers [ 4 , 5 ], while in oxidative atmosphere the

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