2007
DOI: 10.4152/pea.200806503
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Some beta-Aminoketone Derivatives as Corrosion Inhibitors for Nickel in Hydrochloric Acid Solution

Abstract: The use of some β-aminoketone derivatives as corrosion inhibitors for nickel in 2 M acid chloride solution was investigated by gravimetric and galvanostatic polarization techniques. It was found that the investigated compounds behave as inhibitors for nickel dissolution and their inhibition efficiencies increase by the addition of iodide ions. Also, the adsorption isotherms were studied and it was found to follow the Frumkin's adsorption isotherm. By increasing the temperature of the corrosive medium containin… Show more

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Cited by 13 publications
(11 citation statements)
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“…Organic compounds containing hetero atoms in the functional groups, pi-electron in triple or conjugated double bonds and presence of aromatic rings in their structure are the major adsorption centres and are usually good inhibitors [17]. Several heterocyclic compounds such as methylthiophenyl derivatives [18], isoxazolium cationic Schiff base compounds [19], quinoline derivatives [20], sulphonamide compounds [21], thiadiazoles derivatives [22], imidazole derivatives [23], fluoroquinolones [24], pyrazole derivatives [25], pyridazine derivatives [26] and pyridine derivatives [27] have been reported as anticorrosion substances in various corrosive environments.…”
Section: Introductionmentioning
confidence: 99%
“…Organic compounds containing hetero atoms in the functional groups, pi-electron in triple or conjugated double bonds and presence of aromatic rings in their structure are the major adsorption centres and are usually good inhibitors [17]. Several heterocyclic compounds such as methylthiophenyl derivatives [18], isoxazolium cationic Schiff base compounds [19], quinoline derivatives [20], sulphonamide compounds [21], thiadiazoles derivatives [22], imidazole derivatives [23], fluoroquinolones [24], pyrazole derivatives [25], pyridazine derivatives [26] and pyridine derivatives [27] have been reported as anticorrosion substances in various corrosive environments.…”
Section: Introductionmentioning
confidence: 99%
“…The effect of many pyrimidine derivatives namely, 2-aminopyrimidine, 4,6-dihydroxypyrimidine, 2,4-diaminopyrimidine, 2,4-diamino-6-hydroxypyrimidine, 2,4,6-triaminopyrimidine, 4,6-diamino-2-mercaptopyrimidine [7,8], 2,6-dimethylpyrimidine-2-amine, N-Benzylidene-4,6-dimethylpyrimidine-2-amine and 2-[(3,6-dimethylpyridimine-2-ylimino)methyl]-4-nitrophenol [9] in 2 M HCl; thymine, uracil, thymidine and uridine [10], 4,6-dihydroxy-2-mercaptopyrimidine [11], 5-(3,4,5-trimethoxybenzyl)pyrimidine-2,4-diamine [12], benzylidene-pyrimidin-2-yl-amine, (4-methyl-benzylidene)-pyrimidine-2-yl-amine and (4-chloro-benzylidene)-pyrimidine-2-yl-amine [13]…”
Section: Corrosion Inhibitorsmentioning
confidence: 99%
“…The choice for the frequencies of 2 and 5Hz was based on three arguments [18]. The larger peaks were used to calculate the corrosion current density (icorr), the Tafel slopes (β c and β a ) and the causality factors CF-2 and CF-3 [19].…”
Section: Electrochemical Frequency Modulation (Efm)mentioning
confidence: 99%