Evaporation of Electrolyte During SVET Measurements: The Scale of the Problem and the Solutions

The objective of this work is to investigate the scale of the effect of spontaneous solution evaporation during SVET (Scanning Vibrating Electrode Technique) measurements and demonstrate how it biases the final results. When SVET maps are continuously acquired for more than several hours, the measured currents are smaller than expected. This is attributed to solvent (typically water) evaporation which leads to an increase in solution conductivity over time. If this is not considered when converting the measured potential differences into the local current densities, the SVET results display currents smaller than the true ones. Here, this effect is studied with a platinum disk electrode as source of a constant current and a model corroding system consisting of the AA2024/CFRP galvanic couple. Corrective actions are proposed to mitigate the problem, either in the experimental set‐up or as numerical correction

Layered double hydroxide based active corrosion protective sealing of plasma electrolytic oxidation/sol-gel composite coating on AA2024

This work reports a novel approach for growing layered double hydroxide (LDH) films on any plasma electrolytic oxidation (PEO) coated AA2024 independently of the nature of the PEO coating. The specific PEO coating chosen to carry out this work is considered to be not suitable for direct LDH growth because of phase composition and morphological features. In this paper, we describe a new methodology that consists of covering the PEO coating with a thin layer of aluminum oxide based xerogel as the source of aluminate ions for subsequent in-situ LDH growth. X-ray diffraction (XRD) and scanning electron microscope (SEM) images showed a successful formation of LDHs on the surface. An improvement in terms of active corrosion protection was also demonstrated by electrochemical impedance spectroscopy (EIS) and scanning vibrating electrode technique (SVET).publishe

PEO Coatings with Active Protection Based on In-Situ Formed LDH-Nanocontainers

In the present work, for the first time Zn-Al layered double hydroxide (LDH) nanocontainers were grown in-situ on the surface and in the pores of plasma electrolytic oxidation (PEO) layer and then loaded with a corrosion inhibitor to provide an active protection. The developed LDH-based conversion process ensures partial sealing of the pores and provides an effective corrosion inhibition on demand leading to increased fault-tolerance and self-healing properties. The structure, morphology and composition of the LDH-sealed PEO coatings on 2024 aluminum alloy were investigated using SEM, TEM/FIB, XRD and GDOES. Electrochemical impedance spectroscopy and scanning vibrating electrode techniques show a remarkable increase in the corrosion resistance and fault tolerance when PEO coating is sealed with a LDH-inhibitor treatment

Zeolite-based photocatalysts immobilized on aluminum support by plasma electrolytic oxidation

The preparation and properties of zeolite-containing oxide coatings obtained by plasma electrolytic oxidation are investigated and discussed. Pure and Ce-exchanged natural (clinoptilolite) and synthetic (13X) zeolites are immobilized on aluminum support from silicate-based electrolyte. Obtained coatings are characterized with respect to their morphology, phase and chemical composition, photocatalytic activity and anti-corrosion properties. It is observed that all mentioned properties of obtained coatings are dependent on processing time and type of immobilized zeolite. Coatings with Ce-exchanged zeolite show higher photocatalytic activity and more effective corrosion protection than those with pure zeolite. The highest photocatalytic activity is observed for coatings processed in pulsed a DC regime for 30 minutes containing Ce-exchanged 13X zeolite, followed by those containing Ce-exchanged clinoptilolite. Pronounced anti-corrosion properties feature almost all samples containing Ce-exchanged 13X zeolite

The Role of Cu-Based Intermetallic on the Direct Growth of a ZnAl LDH Film on AA2024

The direct ZnAl layered double hydroxide growth on AA2024 is a fast-occurring reaction, yet is characterized by an inhomogeneous film thickness. It has been shown that at the periphery of Cu-rich intermetallic, the flakes tend to be larger and denser. A combination of in situ and ex situ measurements were used to monitor the changes in the layered double hydroxide film grown on the regions of intermetallics. Immediately after immersion, an activation of the intermetallic phases is observed due to the dealloying process with an almost immediate film growth. Dealloying is followed by trenching of the adjacent Al matrix leading to an excessive production of large and dense layered double hydroxide flakes at the periphery of the intermetallic. However, the scanning electron microscopy cross-section images revealed that the trenching process leads to defects in the area surrounding the intermetallic. This could weaken the corrosion resistance performance of the layered double hydroxide conversion coating and lead to adhesion failure of consecutive polymer coatings. Nevertheless, this work highlights a few advantages and drawbacks of the layered double hydroxide conversion coatings and pathways to its potential optimization and improvement

Properties of ZnO/ZnAl2_2O4_4 composite PEO coatings on zinc

Recently the successful formation of PEO coatings on zinc in a phosphate aluminate electrolyte was shown. The produced composite coatings contain various mixtures of ZnO and ZnAl$_2$O$_4$. In frame of the current study, the properties of the formed coatings including adhesion/cohesion, wear, corrosion and photocatalytic activity were analysed to identify possible applications. However, the coatings show internal porosity and a sponge-like structure. Thus the cohesion within the coating is quite low. Pull-off tests have demonstrated clear rupture within the PEO layer at strength values as low as 1 MPa. The photocatalytic activity is limited, in spite of the formation of a higher amount of ZnO at shorter treatment times. Interestingly, the composite coatings of ZnO and higher amounts of ZnAl$_2$O$_4$ spinel showed a higher activity, but not sufficient for fast and effective catalytic cleaning applications

Oxygen nonstoichiometry and magnetic properties of doped manganites La0.7Sr0.3Mn0.95Fe0.05O3-δ

Based on the investigation of the dynamics of changes in the oxygen index (3 – δ) during heating of the samples, the formation of a stressed state in their grains as a result of annealing was established. This results in a decrease in the mobility of oxygen vacancies during the reduction of cations and explains the decrease of released oxygen amount with an increase of δ as well as the heating rate of the samples. It was found that the temperature dependence of the magnetization obeys the Curie–Weiss law and as the oxygen defficiency increases, the Curie temperature for solid solutions decreases. It was found that with an increase of temperature in the low-temperature region, magnetic ordering is disturbed due to the excitation of magnons with a quadratic dependence of the energy from the wave vector, the number of which increases in proportion to T3/2. This results in a decrease in the manganite magnetization. The observed temperature dependence of the magnetization measured in the “field-cooling mode” was approximated taking into account the quadratic and non-quadratic dispersion laws of the magnon spectrum

Impact of Alkali Ions Codoping on Magnetic Properties of La(0.9)A(0.1)Mn(0.9)Co(0.1)O(3) (A: Li, K, Na) Powders and Ceramics

The aim of the work was to check how the introduction of alkali and cobalt ions into a manganese structure can affect the structural disorder and, in consequence, lead to the changes (improvements) of magnetic properties. The high-pressure sintering technique was applied to check if the external factor can modify the magnetization of manganites. Nanocrystalline La0.9A0.1Mn0.9Co0.1O3 (where A is Li, K, Na) powders were synthesized by the combustion technique. The respective powders were used for nanoceramics preparation by the high-pressure sintering technique. The structure and morphology of the compounds were studied by X-ray powder diffraction, scanning electron microscopy and energy-dispersive X-ray spectroscopy. Magnetization studies for all compounds were performed in order to check the changes induced by either codoping or the sintering pressure. It was found that the type of the dopant ion and sintering pressure produced significant changes to the magnetic properties of the studied compounds. Alkali ions lead to the stabilization of Co ions in the +2 oxidation state and the formation of positive exchange interactions Mn3+–Mn4+ and Co2+–Mn4+ and the subsequent increase in remanent magnetization. High sintering pressure leads to a decrease in grain size and reduction of long-range ferromagnetic order and lower magnetization. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.This project has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska‐Curie grant agreement No 778070–TransFerr–H2020‐MSCA‐RISE‐ 2017. Part of this work was developed within the scope of the project CICECO‐Aveiro Institute of Materials, UIDB/50011/2020 and UIDP/50011/2020, financed by national funds through the Portuguese Foundation for Science and Technology/MCTES. The equipment of the Ural Center for Shared Use “Modern nanotechnology” UrFU was used. The work has been supported in part by the Ministry of Science and Higher Education of the Russian Federation under Project № FEUZ‐2020‐0054

Bi-substituted Mg3Al–CO3 layered double hydroxides

publishe