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question. The sampling and analytical design must not interfere with the flowability of matter inside the reactor. Additionally, reaction kinetics are expected to be fast given the residence time is short inside a flow reactor. This calls for raising the

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. Kissinger , HE . Reaction kinetics in differential thermal analysis . Anal Chem . 1957 ; 29 : 1702 – 1706 . 10.1021/ac60131a045 . 18. Augis , JA , Bennett , JE . Calculation of the

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3 by both isothermal and non-isothermal TG. Reaction kinetics by TG The most common experimental technique employed to study kinetics of thermally activated reactions is TG, under the conditions of isothermal and

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Journal of Thermal Analysis and Calorimetry
Authors: V. M. Abdul Mujeeb, K. Muraleedharan, M. P. Kannan, and T. Ganga Devi

the α versus t data corresponding to the ranges, α = 0.15–0.45 and α = 0.5–0.95, showed that the both ranges gave the best fits to contracting square model but with different rate constants, k 1 and k 2 . Description of reaction kinetics using

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Isoconversional analysis of solid state transformations

A critical review. Part I. Single step transformations with constant activation energy

Journal of Thermal Analysis and Calorimetry
Authors: J. Farjas and P. Roura

-6031(97)00023-3 . 3. Vyazovkin , S , Wight , CA . Isothermal and nonisothermal reaction kinetics in solids: in search of ways toward consensus . J Phys Chem A . 1997 ; 101 : 8279 – 8284 . 10.1021/jp971889h

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906204c . 19. Vyazovkin , S , Wight , CA 1997 Isothermal and nonisothermal reaction kinetics in solid: in search of ways toward consensus . J Phys Chem A 101 : 5653 – 5658 10.1021/jp

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Isoconversional analysis of solid-state transformations

A critical review. Part III. Isothermal and non isothermal predictions

Journal of Thermal Analysis and Calorimetry
Authors: J. Farjas and P. Roura

reaction kinetics in solids: in search of ways toward consensus . J Phys Chem A 101 : 8279 – 8284 10.1021/jp971889h . 5. Starink , MJ 2003 The determination of

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; herein, only the most popular are presented. They can be grouped according to the presence of the solid phase, gas phase or of both phases. It is known that the factor hampering an explicit quantification of the reaction kinetics is a complex of carbon (C

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. 9. Vyazovkin , S , Wight , CA . Isothermal and nonisothermal reaction kinetics in solids: In search of ways toward consensus . J Phys Chem A 1997 101 44 8279 – 8284 10.1021/jp971889h

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materials science. The study of reaction kinetics dates back to as early as 1889 when the much celebrated formula for the temperature dependence was proposed by Arrhenius. Research in the field of reaction rates led to the award of the first Nobel

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