Preparation and electrochemical study of cerium-silica sol-gel thin films
Description
Design and development of suitable multilayered systems for delaying corrosion advance in metals requires that both the alteration mechanisms of the metal and the behaviour and properties of the protective coatings be known. Coatings prepared by the sol-gel method provide a good approach as protective layers on metallic surfaces. This kind of coatings can be prepared from pure chemical reagents at room temperature and atmospheric pressure, with compositions in a very wide range of environmentally non-aggressive precursors. Sol-gel coatings based on siloxane bonded units were prepared starting from an organic-inorganic hybrid system. The precursors were γ-methacryloxypropyltrimethoxysilane (MAP) and tetramethoxysilane (TMOS). Cerium nitrate hexahydrate in three different concentrations was added. Cerium salts may perform a similar protective effect to that carried out by the well-known lead oxides and chromium salts, even though in this case a negative environmental impact is not expected. Application of coatings upon pure zinc substrates and common glass slides were performed by spinning. Coated samples were heat treated at 40 deg. C for 6 days. Optical measurements (UV-Vis absorption and diffuse reflectance spectroscopies) pointed out that the coatings were colourless and transparent, reducing the diffuse reflectance of the metallic surface up to ∼60%. Optical and scanning electron microscopies (SEM) allowed observation of the texture and microstructure of the coated samples, both before and after the corrosion tests were carried out. Likewise, the remaining sols were kept to gelify at 60 deg. C for 4 days and then powdered to obtain suitable samples for analysing them by other characterisation techniques (Fourier transformed infrared, FTIR and differential thermal analysis, DTA). Electrochemical measurements were performed by impedance spectroscopy. This technique was used to clarify the anticorrosive protection role of cerium ions incorporated into the hybrid sol-gel network. The effect of cerium concentration on the impedance spectra was analysed, as well as the system behaviour against the corrosive medium (0.6 M NaCl aqueous solutions), as a function of exposure time. From the electrochemical point of view, the sol-gel films behave as a conversion coating on the metallic surface
Additional details
Identifiers
- DOI
- 10.1016/j.jallcom.2004.03.047;
- PII
- S0925838804003391;
Publishing Information
- Journal Title
- Journal of Alloys and Compounds
- Journal Volume
- 380
- Journal Issue
- 1-2
- Journal Page Range
- p. 219-224
- ISSN
- 0925-8388
- CODEN
- JALCEU
Conference
- Title
- 4. international spring workshop on spectroscopy, structure and synthesis of rare earth systems
- Dates
- 21-26 Jun 2003
- Place
- Ladek Zdroj (Poland)
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 37028803
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- AQUEOUS SOLUTIONS; CERIUM IONS; CERIUM NITRATES; CHEMICAL PREPARATION; CORROSION; DIFFERENTIAL THERMAL ANALYSIS; ELECTROCHEMISTRY; FOURIER TRANSFORMATION; INFRARED SPECTRA; LEAD OXIDES; PROTECTIVE COATINGS; SCANNING ELECTRON MICROSCOPY; SILICA; SODIUM CHLORIDES; SOL-GEL PROCESS; TEMPERATURE RANGE 0273-0400 K; THIN FILMS; X-RAY DIFFRACTION
- Descriptors DEC
- ALKALI METAL COMPOUNDS; CERIUM COMPOUNDS; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; CHEMISTRY; CHLORIDES; CHLORINE COMPOUNDS; COATINGS; COHERENT SCATTERING; DIFFRACTION; DISPERSIONS; ELECTRON MICROSCOPY; FILMS; HALIDES; HALOGEN COMPOUNDS; HOMOGENEOUS MIXTURES; INTEGRAL TRANSFORMATIONS; IONS; LEAD COMPOUNDS; MICROSCOPY; MINERALS; MIXTURES; NITRATES; NITROGEN COMPOUNDS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; RARE EARTH COMPOUNDS; SCATTERING; SODIUM COMPOUNDS; SOLUTIONS; SPECTRA; SYNTHESIS; TEMPERATURE RANGE; THERMAL ANALYSIS; TRANSFORMATIONS
Optional Information
- Copyright
- Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.