Secondary carbides precipitated in high chromium cast irons during thermal treatments were characterized by means of different characterization techniques, including scanning electron microscopy, energy dispersive X-ray spectroscopy, electron backscattered diffraction and a combination of chemical etching with confocal scanning laser microscopy. This set of techniques provides a full morphological, chemical and crystallographic description of the analysed phases. This work evaluated different methods for optimizing the image acquisition for a further image analysis (IA) based on the threshold binarization. Finally, the carbide size, distribution and morphology were determined after IA of the images acquired by aforementioned characterization techniques. Although the different techniques report some dispersion in the value for the average particle size, the particle inter-spacing and aspect ratio meet within the error value. The proposed characterization methodology provides statistically reliable data for a further evaluation of related physical properties in composites.
This work evaluates different etching solutions, including Marble, Vilella, RNO and Murakami, used with the purpose of revealing secondary carbides precipitated in high chromium cast irons after heat treatments for their analysis with optical microscopy (OM) and confocal laser scanning microscopy (CLSM) and the posterior binarization of the obtained images. Etching with Marble and Murakami showed the best results for revealing secondary carbides when OM is used for the characterization. The etching parameters to reveal secondary carbides resulted to be different depending on the technique used for their evaluation, i. e. the etching time for a good phase contrast was not the same when an OM or a CLSM is used for the characterization.It was shown that the selection of the proper etchant and etching procedure is of utmost importance for the subsequent particle characterization by means of image analysis. Moreover, the results shown here intend to act as a guide for the optimization of etching parameters with the aim of finding the most suitable solution to reveal the carbides.
Further development of high chromium cast irons (HCCI) is based on tailoring the microstructure, necessitating an accurate control over the phase transformation and carbide precipitation temperatures and can be achieved by thermal treatments (TT). To understand the underlying mechanisms controlling the transformation kinetics during the different stages of the TT, it is imperative to adjust the TT parameters to have information of the transformations occurring during non-thermal and isothermal heating cycles, since proper selection of the TT parameters ensures the optimum use of the alloying elements. In this work, the boundaries of the phase transformations for a HCCI containing 26 wt pct Cr for different cooling rates (continuous cooling transformation, CCT, diagram) were established by applying dilatometric measurements. Based on the CCT diagram, a temperature-time-transformation (TTT) diagram was constructed by isothermally holding the samples until complete phase transformation. For determining the initiation and finishing of the transformation, the lever rule assisted by derivatives was applied. The phases present after transformation were determined by combining X-ray diffraction (XRD) and metallographic characterization using optical microscopy (OM) and scanning electron microscopy (SEM). Finally, the data obtained from the dilatometer was experimentally verified by isothermally heat treating some samples using laboratory furnaces. The transformed phase fraction from OM and SEM images was then correlated to the fraction obtained from the TTT diagram.
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.