Inhibitive action of the octyl esters of 4-and 5-carboxybenzotriazole for copper corrosion in sulphate solutions

Citation
N. Huynh et al., Inhibitive action of the octyl esters of 4-and 5-carboxybenzotriazole for copper corrosion in sulphate solutions, CORROS SCI, 42(2), 2000, pp. 259-274
Citations number
30
Categorie Soggetti
Material Science & Engineering
Journal title
CORROSION SCIENCE
ISSN journal
0010938X → ACNP
Volume
42
Issue
2
Year of publication
2000
Pages
259 - 274
Database
ISI
SICI code
0010-938X(200002)42:2<259:IAOTOE>2.0.ZU;2-Z
Abstract
The inhibitive action of a mixture of the octyl esters of 4- and 5-carboxyb enzotriazole (4-CBTAH-OE and 5-CBTAH-OE) for copper in aerated 0.5 M sulpha te solution over a range of pH values (0-8) was investigated. Coupon tests showed that at pH similar to 0 the inhibition efficiency of the mixture was approximately 98% at the 1 x 10(-4) M level, This is considerably higher t han that for benzotriazole (BTAH) (similar to 50%) under similar conditions . At pH similar to 8 the inhibition efficiency is still appreciable (simila r to 75%) indicating that the mixed esters (in contrast to BTAH) have pract ical application for the inhibition of copper corrosion over a relatively w ide pH range. Over the pH range no hydrolysis of the esters was observed. S urface enhanced Raman scattering (SERS) indicated that the esters, like BTA H, inhibit copper corrosion at low pH by chemisorption of the protonated sp ecies (CBTAH(2)(+)-OE) on the metal through an azole nitrogen. The increase d inhibition at low pH is attributed to van der Waals' forces of attraction brtween adjacent octyl chains oriented away from the copper surface. SERS also suggest that at higher pH chemisorption is replaced by the deposition of a sterically hindered polymeric complex that. in contrast to BTAH, is no t as protective as chemisorbed CBTAH(2)(+)-OE. Potentiodynamic polarisation also supports the changeover to a different protective mechanism as the pH is raised. (C) 2000 Elsevier Science Ltd. All rights reserved.