Conventional ferrous powder metallurgy relies on uniaxial die-pressing of powder before sintering. The operation causes particle rearrangement and deformation and the initial state of the compact ultimately determines the sintering behaviour. In this study, sintering was investigated for water-atomised iron powder compacted at three different pressure levels, with and without admixed graphite. Electron back-scatter diffraction of the powder and compacts showed a large increase in low-angle grain boundaries after compaction. The sintering of the compacts was investigated by means of dilatometry in hydrogen. The initial compaction strongly influences sintering shrinkage, particularly in the low-temperature, high-diffusivity ferrite region which can account for up to 80% of the recorded shrinkage. Only a small fraction of the total shrinkage originates from the austenite phase, even at high sintering temperatures. However, the ratio of sintering shrinkage in ferrite and austenite changes with compaction pressure, carbon content and heating rate.
High sinter density is desired in powder metallurgy components as the requirement for performance is increasing day‐by‐day. One of the promising ways to achieve improved densification during sintering is through the addition of nanopowder to the conventional micrometer sized metal powder. It is well known that the surface chemistry of the powder has a decisive effect on sintering and consequently the properties of the components produced. Extensive research has hence been conducted to elucidate the surface chemistry and its influence on sintering for powder used in conventional powder metallurgy. Nanopowder, owing to high surface to volume ratio, can contribute to the activation of sintering at lower temperatures and enhance the sinter density. In this context, the surface chemistry of the nanopowder is also expected to exhibit substantial influence on sintering. The present investigation is aimed at establishing a methodology to study the surface chemistry and oxide thickness of nanopowder. For this purpose, iron nanopowder of 3 different size fractions: 35 to 45, 40 to 60, and 60 to 80 nm with core‐shell structure were studied. Different approaches were adopted to evaluate the shell thickness of the iron nanoparticles. The methodology was developed and tried on low alloy steel nanopowder to measure oxide thickness. X‐ray photoelectron spectroscopy, thermogravimetry, and high‐resolution scanning electron microscopy techniques were used to study the nanopowder. Results from different core‐shell models for iron nanopowder were found to be consistent except in the case where depth profiling was taken into account. The results were in agreement with the values obtained from thermogavimetry‐surface area correlation.
Iron nanopowder could be used as a sintering aid to water-atomised steel powder to improve the sintered density of metallurgical (PM) compacts. For the sintering process to be efficient, the inevitable surface oxide on the nanopowder must be reduced at least in part to facilitate its sintering aid effect. While appreciable research has been conducted in the domain of oxide reduction of the normal ferrous powder, the same cannot be said about the nanometric counterpart. The reaction kinetics for the reduction of surface oxide of iron nanopowder in hydrogen was therefore investigated using nonisothermal thermogravimetric (TG) measurements. The activation energy values were determined from the TG data using both isoconversional Kissinger–Akahira–Sunose (KAS) method and the Kissinger approach. The values obtained were well within the range of reported data. The reaction kinetics of Fe2O3 as a reference material was also depicted and the reduction of this oxide proceeds in two sequential stages. The first stage corresponds to the reduction of Fe2O3 to Fe3O4, while the second stage corresponds to a complete reduction of oxide to metallic Fe. The activation energy variation over the reduction process was observed and a model was proposed to understand the reduction of surface iron oxide of iron nanopowder.
A promising method of improving the densification of powder metallurgical steel components is to blend nanopowder with the otherwise typically used micrometre-sized powder. The higher surface-to-volume ratio of nanopowder is hypothesized to accelerate the sintering process and increase the inter-particle contact area between the powder particles. This is supposed to enhance the material transport and improve the densification. In the present investigation, water-atomized iron powder (− 45 μm) was mixed separately with pure iron and low-carbon steel nanopowder, each at a ratio of 95 to 5 pct. These powder mixes were compacted at different pressures (400, 600 and 800 MPa) and then sintered at 1350 °C in a pure hydrogen atmosphere. The sintering behavior of the powder blend compacts was compared to that of the compact with micrometre-sized powder only. Densification commenced at much lower temperatures in the presence of nanopowder. To understand this, sintering at intermittent temperatures such as 500 °C and 700 °C was conducted. The fracture surface revealed that the nanopowder was sintered at between 500 °C and 700 °C, which in turn contributed to the densification of the powder mix at the lower temperature range. Based on the sintering experiments, an attempt was made to calculate the activation energy and identify the associated sinter mechanism using two different approaches. It was shown that the first approach yielded values in agreement with the grain-boundary diffusion mechanism. As the nanopowder content increased, there was an increase in linear shrinkage during sintering.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.