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Effect of surfactant concentration in modifying solution on corrosion properties of the coatings based on vinyltrimethoxysilane (VTMS) and poly(3,4-ethylenedioxythiophene) (PEDOT)

Kucharczyk A., Adamczyk Lidia, Miecznikowski K.

Archives of Materials Science and Engineering

2023

Vol. 121, nr 1

5--17

Purpose: This paper presents an analysis of the structure and physicochemical properties of coatings based on an organofunctional silane (VTMS), a conductive polymer (PEDOT), and a surfactant (polyoxyethylene glycol monolauryl ether BRIJ). Design/methodology/approach The coatings were deposited on X20Cr13 stainless steel and glassy carbon specimens using sol-gel immersion. The obtained coatings were characterised in terms of topography, microstructure, roughness, adhesion to the steel substrate, thickness, and corrosion resistance. Corrosion tests were conducted in sulfate environments with pH = 2 without or with the addition of Cl- ions. Findings: The use of different surfactant concentrations in the modifying solution is intended to improve the deposition efficiency and increase the degree of dispersion of silane and conducting polymer. Research limitations/implications The tested coatings were found to slow down the corrosion of the steel substrate, thus effectively protecting it from this phenomenon. The use of a surfactant compound is intended to increase the degree of dispersion of silane and polymer in the modifying solution to improve deposition efficiency. Practical implications: Test carried out in corrosive media have shown that the coatings proposed in the above work, based on VTMS silane, PEDOT polymer and BRIJ surfactant, significantly increase the corrosion resistance of the tested materials, which confirms their effectiveness and possibility of application in various industries. Originality/value: The novelty of this paper is the use of silane (VTMS), polymer (PEDOT) and surfactant (BRIJ) as components of the anticorrosion coating.

Aktywacja platynowego katalizatora redukcji tlenu dla potrzeb niskotemperaturowego ogniwa wodorowo-tlenowego

Kolary-Żurowska A., Miecznikowski K., Kulesza P. J.

Przemysł Chemiczny

2008

T. 87, nr 1

52-54

Two-Layer Structures of Ultra-Thin Metal Hexacyanoferrate Films: Charge Trapping Possibility of Application to Corrosion Protection

Miecznikowski K., Chojak M., Steplowska W., Makowski O., Kulesza P., Adamczyk L., Malik M., Gałkowski M., Bala H.

Polish Journal of Chemistry

2004

Vol. 78 / nr 9

1183-1193

The possibility of fabrication of ultra-thin films of metal hexacyanoferrates, Prussian Blue, PB, and nickel hexacyanoferrate, NiHCNFe, by multiple sequential attachment of metal cations (self-assembled on 4-aminobenzoic acid monolayer) and hexacyanoferrate anions, has been demonstrated. These films can form a bilayer arrangement on glassy carbon when PB and NiHCNFe are deposited as inner and outer films, respectively. To avoid mixing of the NiHCNFe and PB redox sites, we introduce an polymer interlayer from poly(4-vinylpyridine) and Nafion. Since the outer NiHCNFe film is physically separated from the electrode surface, and it undergoes redox reactions at potentials characteristic of the inner PB film, an effect of the reversible charge state trapping (bistable switching) is observed. Astable bilayer structure can also be deposited on stainless steel. The whole concept may be of importance to corrosion protection since charge accumulated in the oxidized bilayer film tends to stabilize corrosion potential within passive range.