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Corrosion Rate and Mechanism of Degradation of Chitosan/TiO2 Coatings Deposited on MgZnCa Alloy in Hank's Solution
Faculty of Foundry Engineering, AGH University of Krakow, Krakow, Poland.
Faculty of Foundry Engineering, AGH University of Krakow, Krakow, Poland.
Faculty of Foundry Engineering, AGH University of Krakow, Krakow, Poland.
Polytechnic Department of Engineering and Architecture, University of Udine, Udine, Italy.
Vise andre og tillknytning
2024 (engelsk)Inngår i: International Journal of Molecular Sciences, ISSN 1661-6596, E-ISSN 1422-0067, Vol. 25, nr 10, artikkel-id 5313Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Overly fast corrosion degradation of biodegradable magnesium alloys has been a major problem over the last several years. The development of protective coatings by using biocompatible, biodegradable, and non-toxic material such as chitosan ensures a reduction in the rate of corrosion of Mg alloys in simulated body fluids. In this study, chitosan/TiO2 nanocomposite coating was used for the first time to hinder the corrosion rate of Mg19Zn1Ca alloy in Hank's solution. The main goal of this research is to investigate and explain the corrosion degradation mechanism of Mg19Zn1Ca alloy coated by nanocomposite chitosan-based coating. The chemical composition, structural analyses, and corrosion tests were used to evaluate the protective properties of the chitosan/TiO2 coating deposited on the Mg19Zn1Ca substrate. The chitosan/TiO2 coating slows down the corrosion rate of the magnesium alloy by more than threefold (3.6 times). The interaction of TiO2 (NPs) with the hydroxy and amine groups present in the chitosan molecule cause their uniform distribution in the chitosan matrix. The chitosan/TiO2 coating limits the contact of the substrate with Hank's solution.

sted, utgiver, år, opplag, sider
MDPI, 2024. Vol. 25, nr 10, artikkel-id 5313
Emneord [en]
TiO2 nanoparticles, chitosan, coating, corrosion rate, magnesium alloy
HSV kategori
Identifikatorer
URN: urn:nbn:se:hj:diva-64578DOI: 10.3390/ijms25105313ISI: 001233311300001PubMedID: 38791360Scopus ID: 2-s2.0-85194219928Lokal ID: GOA;intsam;954467OAI: oai:DiVA.org:hj-64578DiVA, id: diva2:1864327
Forskningsfinansiär
European Commission, H2020-MSCA-ITN-2017, 764977Tilgjengelig fra: 2024-06-03 Laget: 2024-06-03 Sist oppdatert: 2025-10-13bibliografisk kontrollert

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