DocumentCode
2496762
Title
Activation Energy of Solute Migration in a Gas-Solid Chromatography
Author
Zhang Dali ; Ke Jiajun ; Lu Lizhu
Author_Institution
Biochem. Eng. Coll., Beijing Union Univ., Beijing, China
fYear
2009
fDate
11-13 June 2009
Firstpage
1
Lastpage
3
Abstract
The rate equation of solute migration for a gas-solid chromatography was derived from Maxwell distribution of energy and the principle of equipartition of energy. Different from two-phase distribution ratio being used to explain the retention time of solute in plate theory, the retention time was explained with the activation energy of migration from a new and kinetic viewpoint. According to the derivation of the rate equation for solute migration, the activation energy of migration related to the kinetic energy of translation, rotation and vibration. Temperature observably influenced the activation energy of migration. Separation mechanism of gas-solid chromatography was based upon different solutes having different functions of physical adsorption on the stationary phase. This property could be the cause of the activation energy of migration being different from reaction activation energy in nature. The activation energy of migration for alkane homolog increased with carbon number. To investigate the mechanism of gas-solid chromatography was attempted from a kinetic viewpoint, in order to provide some ideal at understanding chromatography process.
Keywords
chromatography; diffusion; reaction kinetics; solutions; Maxwell energy distribution; activation energy; energy equipartition principle; gas-solid chromatography; plate theory; rate equation; retention time; separation mechanism; solute migration; two-phase distribution ratio; Cathode ray tubes; Educational institutions; Entropy; Kinetic energy; Kinetic theory; Maxwell equations; Maxwell-Boltzmann distribution; Power engineering and energy; Temperature;
fLanguage
English
Publisher
ieee
Conference_Titel
Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
Conference_Location
Beijing
Print_ISBN
978-1-4244-2901-1
Electronic_ISBN
978-1-4244-2902-8
Type
conf
DOI
10.1109/ICBBE.2009.5162270
Filename
5162270
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