Document Details

Document Type : Article In Journal 
Document Title :
Kinetic-thermodynamic and adsorption isotherms analyses for the inhibition of the acid corrosion of steel by cyclic and open-chain amines
Kinetic-thermodynamic and adsorption isotherms analyses for the inhibition of the acid corrosion of steel by cyclic and open-chain amines
 
Subject : Chemistry 
Document Language : English 
Abstract : The corrosion inhibition characteristics of the quadridentate macrocycle 1, 4, 8, 11 tetra-azacyclotetradecane (cyclam) on steel in sulfuric acid media are investigated at 25,35,45, and 55°C, and the thermodynamic energy parameters calculated. In addition the inhibition characteristics of the open-chain polydentate amines, ethylenediamine (en), diethylenetriamine (dien), triethylenetetraamine (trien), and tetraethylenepentamine (tetren) were investigated at 25°C. Activation-free energies, enthalpies, and entropies for the inhibition process of both cyclam and tetren were determined from the rate constants data measured at four temperatures viz, 25, 35, 45, and 55°C at one or two fixed inhibitor concentrations. All data were compared and fitted to a previously published kinetic-thermodynamic model in terms of an active site occupancy parameter y and a binding constant K of the inhibitor to the active site. The results obtained are compared with fits obtained from the application of Fumkin and Flory-Huggins adsorption isotherms. The first isotherm attempts to treat the deviations from the ideal Langmuir isotherm by the use of a lateral interaction parameter a while the second uses a relative-size parameter x which is a measure of the relative size of the inhibitor molecule to the surface-adsorbed water molecule. Good agreement was obtained between the kinetic-thermodynamic and Flory-Huggins models. The Frumkin isotherm model, however, agreed only in cases where the active site occupancy, or the relative-size parameters were equal to or close to unity. A discussion of the strengths and weaknesses of each treatment is given. In addition, the results obtained are correlated to the chemical structure of the inhibitors, the number of donor atoms, and the macrocyclic effect. 
ISSN : 0013-4651 
Journal Name : Journal of the Electrochemical Society 
Volume : 139 
Issue Number : 8 
Publishing Year : 1413 AH
1992 AD
 
Article Type : Article 
Added Date : Monday, December 26, 2011 

Researchers

Researcher Name (Arabic)Researcher Name (English)Researcher TypeDr GradeEmail
عباس عباس العوضيEl-Awady, Abbas AResearcherDoctorateabbaselawady@hotmail.com
Beshier A Abd-El-NabeyAbd-El-Nabey, Beshier AResearcherDoctorate 
سعدالله قاري عزيزAziz, Saadullah GResearcherDoctoratesaziz@kau.edu.sa

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