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Amino acids as corrosion inhibitors for copper in acidic medium: Experimental and theoretical study
Author(s) -
Ingrid Milošev,
Jasminka Pavlinac,
Milan Hodošček,
Antonija Lesar
Publication year - 2013
Publication title -
journal of the serbian chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.227
H-Index - 45
eISSN - 1820-7421
pISSN - 0352-5139
DOI - 10.2298/jsc131126146m
Subject(s) - amino acid , cysteine , chemistry , molecule , electrochemistry , adsorption , molecular dynamics , protonation , copper , alanine , density functional theory , corrosion , electrolyte , reactivity (psychology) , functional group , computational chemistry , inorganic chemistry , organic chemistry , ion , electrode , biochemistry , medicine , alternative medicine , pathology , enzyme , polymer
Experimental electrochemical methods combined with quantum chemical calculations and molecular dynamics simulations were used to investigate the possibility of use various amino acids as “green” corrosion inhibitors for copper in 0.5 M HCl solution. Among eleven amino acids studied, cysteine achieved the highest inhibitor effectiveness reaching 52% at 10 mM concentration. Other amino acids reached achieved effectiveness less than 25%, some of them even acted as corrosion accelerators. Based on the experimental results, theoretical calculations and simulations were focused on cysteine and alanine. The electronic and reactivity parameters of their protonated forms in electrical double layer were evaluated by density functional calculations. In addition, molecular dynamic simulations were introduced to follow the adsorption behaviour of these two amino acids at the Cu(111) surface in the electrolyte solution. The results indicate that the orientation of both molecules is nearly parallel to the surface except of ammonium group which is directed away from the surface. Therefore, as the orientation of the cysteine and alanine molecules at the surface is similar, thiol functional group is responsible for superior inhibition efficiency of cysteine

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