OAR@UM Collection:
/library/oar/handle/123456789/63162
2025-11-07T19:23:48ZSol-gel coatings for the protection of ferrous heritage metal
/library/oar/handle/123456789/64004
Title: Sol-gel coatings for the protection of ferrous heritage metal
Abstract: Ferrous Iron corrodes when exposed to indoor uncontrolled climates as is the case with Heritage
Metal (HM) being showcased openly in a museum. One way of protecting metals from corrosion is
by applying protective coatings. This work proposes a novel way of protecting HM through the
application of organic-inorganic hybrid (OIH) silica coatings produced through the sol-gel method
as opposed to more conventionally used coatings such as acrylates or nitrocellulose-based lacquers.
Several precursors (X–Si(OR)3) were studied for their anti-corrosion properties, namely X= methyl,
n-propyl-, n-hexyl-, n-octyl- and phenyl-triethoxysilane with tetraethyl orthosilicate (TEOS) in
various mol% ratios (X–Si(OR)3:TEOS). Coating systems involving mixtures of X–Si(OR)3:TEOS
displayed similar trends in their corrosion behaviour: the corrosion resistance of the coatings
improves with increasing organic content reaching a maximum, the corrosion resistance is then
observed to drop again with further organic loading. These observations have been explained through
their mechanical properties. Higher silica content leads to harder, more well-adhered coatings;
however, if the silica content is too high then brittle coatings form. On the other hand, if the coating
contains a large portion of organics, then coatings will be softer and show poor adhesion, even though
hydrophobicity is improved. OTES:TEOS 20:80 mol% and MTES:TEOS 60:40 mol% were further
considered and applied onto corroded surfaces and their extent of corrosion protection on such a
surface was also evaluated. Crack formation was visibly reduced by increasing the silica
concentration, thus resulting in thicker coatings and though the increase in XTES:TEOS ratio, both
leading to an improvement in corrosion protection.
OIH alkoxysilane coatings impregnated with silica nanoparticles and in/organic chemical inhibitors
have been considered in this work. Nanoparticles having a diameter of 10-20 nm purchased
commercially (Commercial Nanoparticles, CNPs) produced a slight improvement in corrosion
protection. Nanoparticles developed through a bottom up approach, the Stöber method (Stöber nanoparticles, SNPs) did not bring about an improvement in corrosion protection. More protective
coatings were obtained on clean metal with in/organic inhibitor molecules when added to MTES
sols, at a given concentration of inhibitor for all six inhibitors studied. This was not the case with
OTES coatings for which only one of the six molecules produced an improvement over the blank
coating.
A comparative study was drawn between OIH silane coatings and conventionally used lacquers for
HM namely, Paraloid B-48, B-72 and Ercalene. Electrochemical testing carried out on dip-coated
clean metal coupons revealed OIH silane coatings to be more protective than the lacquers. This was
not the case on corroded surfaces where OIH coating were found to be less protective than the
lacquers which has been attributed to the thickness of coatings. For accelerated corrosion testing,
thicker coatings were applied using both dip and brush application, the latter being a frequently used
mode of application by conservators. OIH alkoxysilane coatings were significantly more protective
than lacquers using both applications. Finally, a reversibility study on all OIH silane coatings was
conducted where it was determined that all coatings can be removed using a mixture of sodium
hydroxide solution with isopropyl alcohol solvent. This thesis proves the suitability of OIH silanes
as coatings for HM since they are transparent and do not affect the aesthetics of the object, are applied
without affecting the microstructure of the metal, provide significant corrosion protection which
exceed that offered by conventional lacquers, and can be removed with relative ease.
Description: PhD2019-01-01T00:00:00Z