Use In Magnetic Applications Research Articles

Influence of Te-Incorporated LaCoO3 on Structural, Morphology and Magnetic Properties for Multifunctional Device Applications.

A high perovskite activity is sought for use in magnetic applications. In this paper, we present the simple synthesis of (2.5% and 5%) Tellurium-impregnated-LaCoO3 (Te-LCO), Te and LaCoO3 (LCO) by using a ball mill, chemical reduction, and hydrothermal synthesis, respectively. We also explored the structure stability along with the magnetic properties of Te-LCO. Te has a rhombohedral crystal structure, whereas Te-LCO has a hexagonal crystal system. The reconstructed Te was imbued with LCO that was produced by hydrothermal synthesis; as the concentration of the imbuing agent grew, the material became magnetically preferred. According to the X-ray photoelectron spectra, the oxidation state of the cobaltite is one that is magnetically advantageous. As a result of the fact that the creation of oxygen-deficient perovskites has been shown to influence the mixed (Te4+/2-) valence state of the incorporated samples, it is abundantly obvious that this process is of utmost significance. The TEM image confirms the inclusion of Te in LCO. The samples start out in a paramagnetic state (LCO), but when Te is added to the mixture, the magnetic state shifts to a weak ferromagnetic one. It is at this point that hysteresis occurs due to the presence of Te. Despite being doped with Mn in our prior study, rhombohedral LCO retains its paramagnetic characteristic at room temperature (RT). As a result, the purpose of this study was to determine the impacts of RT field dependency of magnetization (M-H) for Te-impregnated LCO in order to improve the magnetic properties of RT because it is a low-cost material for advanced multi-functional and energy applications.

An innovative magnetic oxide dispersion-strengthened iron compound obtained from an industrial byproduct, with a view to circular economy

Since the policy of Sustainable Production and Consumption has laid the basis for the world to begin its transition towards a circular economy, engineering has a moral responsibility to recycle industrial byproducts. This is currently done with calamine, which is a mill scale resulting from high temperature steel manufacturing. Although calamine is used in different ways, it could be given greater added value by subjecting it to processing by powder metallurgy. Therefore, the aim of this study was to obtain powder from iron with a core of enriched magnetite iron oxide, and to evaluate the effect of this iron oxide nucleus on the hardness and magnetic properties of the material after sintering. It was found that iron oxide acts as a reinforcement for iron (the highest achieved hardness was 77.7 ± 1.2 HRB) due, in part, to the coherency between phases, and confers a ferrimagnetic behavior to it. Therefore, this material has potential for use in magnetic applications at higher frequencies than current soft materials.

(Invited) Characterisation of Metal Deposition and Metal Dissolution Processes in Deep Eutectic Solvents Using Electrochemical, Gravimetric and Neutron Scattering Methods

Electrolytic coatings of metals such as nickel, chromium, zinc, silver and gold are commonly applied as decorative and/or functional coatings. Some of the functional benefits which metal coatings provide are corrosion resistance, wear resistance, electrocatalysis and use in magnetic applications. A range of strategic manufacturing industries are dependent on such electrolytic coatings including electronics, aerospace, automotive and energy. The vast majority of electrolytic coatings are plated from aqueous solutions but stringent health and safety legislation governing transport, use and disposal of feedstock chemicals has driven the challenge for innovation in electrolyte technology that facilitates coatings from less toxic materials and in a manner that is more efficient and more consistent with environmental and process sustainability. We have been motivated by this challenge and have developed a range of novel solvent systems for deposition of metal coatings as alternatives to existing process (e.g. Ni, Zn, Cu, Ag, Ag) as well as novel electrolytes for deposition of reactive metals such as Al. These electrolytes have become known as Deep Eutectic Solvents and have shown utility and promise in a range of metal finishing processes. [1] Whilst the thermodynamics, kinetics, metal ion speciation and growth processes of electrolytic coatings from aqueous solutions have been studied for more than one hundred years, little is currently known about these fundamental aspects of electrochemical deposition from DES media. [2] Here we describe our studies into the electrochemical characterisation of a range of metals in DES electrolytes. In particular, we will focus on aspects of growth and dissolution processes and how these effect the morphology and composition of metal films. We will describe the characterisation of thin metal films in DES media using a range of time resolved techniques including cyclic voltammetry, chronopotentiometry, chronoampertometry, gravimetry (QCM), neutron reflectometry (NR) and surface metrology. The use of in-situ electrochemical NR methods is novel and we will present new data on the growth and dissolution of single metal and bi-layer metals films. The Figure shows time resolved NR data for the electrochemical dissolution of a Cu/Ag bi-layer on a Au substrate. We will also present complimentary data on the characterisation of the same systems using so-called Simultaneous Thickness Electrochemical Potential (STEP) chronopotentiometric methods. We will consider the effect of small-molecule additives on surface morphology and finish (roughness) of electrolytic coatings. [3] Organic and inorganic additives are often added to electroplating solutions to improve surface finish, reduce roughness and promote uniform surface morphology of the coatings. Such additives are usually small molecules and often referred to as brighteners or levellers. However, there have been limited investigations into the effect of such additives on electrodeposition from ionic liquids (ILs) and deep eutectic solvents (DESs). Here we will describe the effect of four additives on electrolytic plating of exemplar metals, nickel and zinc, from an ethyleneglycol based DES; these are nicotinic acid (NA), methylnicotinate (MN), 5,5-dimethyl- hydantoin (DMH) and boric acid (BA). The additives show limited influence on the bulk speciation but have significant influence on the electrochemical behaviour of metal deposition. Small concentrations (ca. 15 mM) of NA and MN show inhibition of metal ion reduction whereas high concentrations of DMH and BA are required for a modest difference in behaviour from the additive free system. NA and MN also show that they significantly alter the nucleation and growth mechanism when compared to the additive free system and those with DMH and BA. Each of the additive systems had the effect of producing brighter and flatter bulk electrodeposits and with increased coating hardness. “Deep Eutectic Solvents (DESs) and their Applications”, Emma L. Smith, Karl S. Ryder and Andrew P. Abbott, Chem. Rev., 2014, 114, 11060.“EXAFS Study into the Speciation of Metal Salts Dissolved in Ionic Liquids and Deep Eutectic Solvents”, Jennifer M. Hartley, Chung-Man Ip, Gregory C.H. Forrest, Kuldip Singh, Stephen J. Gurman, Karl S. Ryder, Andrew P. Abbott and Gero Frisch, Inorg. Chem., 2014, 53(12), 6280.“Bright Metal Coatings from Sustainable Electrolytes: The Effect of Molecular Additives on Electrodeposition of Nickel from a Deep Eutectic Solvent”, Andrew P. Abbott, Andrew Ballantyne, Robert C. Harris, Jamil A. Juma and Karl S. Ryder, Phys. Chem. Chem. Phys., 2017, 19. 3219. Figure 1

Characterization of Mn–Zn Ferrite Prepared by a Hydrothermal Process From Used Dry Batteries and Waste Steel Pickling Liquor

In this study, we propose a process to prepare Mn–Zn ferrite powder, using oxides of manganese and zinc extracted from used dry batteries, and ferrous chloride solution from waste steel pickling liquor. The hydrothermal process was used to convert the starting raw materials into Mn–Zn ferrite powder. This powder revealed the formation of cubic ferrite with a saturation magnetization (Ms) of 58.8 emu/g and an intrinsic coercive force (Hc) of 3.8 Oe. The average lattice thermal expansion coefficient αa (200°–500°C) of this Mn–Zn ferrite powder was 14.14 × 10−6 K−1. The toroidal specimen sintered at 1300°C in a controlled oxygen atmosphere presented a flat profile of initial permeability (μi) of 2150–2200, in the frequency range 0.1–20 kHz, which allows its use in magnetic applications. This useful technology, combined with environment and materials engineering, can promote the recycling of dry batteries and contribute to the preservation of the earth. Moreover, this technology can also decrease the cost of disposal of the used dried batteries and waste steel pickling liquor.