Kp. Ishida et Pr. Griffiths, Investigation of polysaccharide adsorption on protein conditioning films by attenuated total reflection infrared spectrometry - II. Thin copper films, J COLL I SC, 213(2), 1999, pp. 513-524
The study of microorganisms at the aqueous/metal interface is of great inte
rest as their presence is often associated with surface deterioration or co
rrosion. Surfaces submerged in aquatic environments rapidly become fouled w
ith organic macromolecules, such as proteins and/or glycoproteins. Bacteria
adhering to this conditioning film typically produce extracellular polysac
charides that anchor the cells to the substrate. In a previous paper, the k
inetics of polysaccharide adsorption and desorption on protein conditioning
films formed on bare germanium internal reflection elements (IREs) were in
vestigated in an effort to gain a better understanding of the fouling proce
ss. This work has been extended to the study of adsorption phenomena at an
aqueous/copper interface. Alginic acid and dextran were exposed to protein-
conditioned and untreated copper films. In the absence of a protein biofilm
, greater erosion of the Cu film was observed with flowing saline than with
a solution of alginic acid in saline, and more Cu was removed at pH 4.8 th
an at pH 7.0. The neutral polysaccharide was less corrosive than alginic ac
id. The presence of a film of bovine serum albumin (13.5 nm) conditioning f
ilm did not shield the Cu film from the corrosive effects of either polysac
charide. In all experiments, as Cu slowly eroded from the surface of the IR
E, metal islands formed leading to the observation of surface-enhanced infr
ared absorption (SEIRA). The intensity of the C-O stretching band of adsorb
ed dextran on Cu islands was over an order of magnitude greater than would
be observed with a uniform Cu him of the same thickness. Enhancement of the
amide II band of BSA was also observed. In general, the effect of SEIRA co
mplicated spectral processing and interpretation and thus interfered with t
he determination of surface coverage and polysaccharide adsorption/desorpti
on kinetics on protein conditioning films. (C) 1999 Academic Press.