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
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.