Non-isothermal dehydration kinetic study of a new swollen biopolymer silver nanocomposite hydrogel

被引:11
作者
Sovizi, Mohammad Reza [1 ]
Fakhrpour, Ghasem [1 ]
Bagheri, Saleh [2 ,4 ]
Bardajee, Ghasem Rezanejade [3 ]
机构
[1] Malek Ashtar Univ Technol, Dept Chem, Tehran, Iran
[2] Islamic Azad Univ, Fac Chem, Dept Phys & Theoret Chem, Tehran 1913674711, Iran
[3] Payame Noor Univ, Dept Chem, Tehran, Iran
[4] Islamic Azad Univ, Kerman Branch, Dept Chem, Kerman, Iran
关键词
Non-isothermal dehydration; Silver nanocomposite hydrogel; Thermogravimetric analysis; Kinetic; Swollen biopolymer; THERMAL-DECOMPOSITION; PARAMETERS; BEHAVIOR;
D O I
10.1007/s10973-015-4639-4
中图分类号
O414.1 [热力学];
学科分类号
摘要
Thermal dehydration kinetic of a novel swollen silver nanocomposite hydrogel (SNH), prepared based on poly(acrylic acid) grafted onto salep as a water soluble polysaccharide backbone, was studied by thermogravimetry under non-isothermal conditions. The values of apparent activation energies (E-a) and pre-exponential factors (A) for a set of reaction models at 5, 10, 15, and 20 K min(-1) heating rates were determined. The dependence of the activation energy on the extent of conversion was obtained by the model-free methods. Apparent activation energy (E-a) of the process was calculated from Kissinger-Akahira-Sunose and Tang isoconversional methods. From the strong dependence of the E-a value on the extent of conversion (alpha) for the investigated process, it was found that the dehydration process of SNH is complex and we cannot explain the whole process by a single mechanism. In the low extent of conversion (alpha), E-a rapidly decreases and the dehydration process is complex and probably involving a combination of several processes. In the range of alpha = 0.40-0.90, E-a is nearly constant and the dehydration process can be assumed to follow a single-step reaction. The results obtained from Criado and Invariant kinetic methods, in the constant-E-a region, confirmed that probable model for the dehydration process agreed with R3 model.
引用
收藏
页码:1383 / 1391
页数:9
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