Due to its special properties, boron compounds are developed by numerous ways, .i.e. boronizing gas, molten salt boronizing, with and without electrolysis and pack boronizing. Pack boronizing have attracted increasing interest from the technological and scientific point of view, further it has the advantage of simplicity and cost-effectiveness with other boronizing techniques [1]. Wearing resistance, toughness and corrosion, oxidation resistance, and hardness are some of the properties that are significantly enhanced by this thermochemical diffusion process [2][3][4]. These interesting properties are related with the microstructure that make these coatings excellent candidates to use in applications involving sliding contact and abrasion wear situations [5]. The phase formed in the substrate, its thickness and morphology have interest for study because they are related to their properties. In the present study, the microstructural characterization of iron borides developed at different temperatures by pack-boronizing has been carried out in a AISI 1040 carbon steel and a AISI D2 alloy steel.The AISI 1040 and AISI D2 were borided. The samples had a disc shape with a diameter of 18 mm and a thickness of 3 mm. Prior to the boriding process; the samples were polished, ultrasonically cleaned in an alcohol solution and deionized water for 15 minutes at room temperature, and dried and stored under clean-room conditions. Then the samples were embedded in a closed cylindrical case, containing a fresh Durborid powder mixture. The active boron is then supplied by the powder quantity placed over and around the material surface. The powder-pack boriding process was performed in a conventional furnace under a pure argon atmosphere. The boriding process was carried out at two different temperatures 1220 K and 1320 K for a time of 8 h. The boriding temperatures were selected according to the position of the solidus line in the Fe-B phase diagram. Once the treatment was completed, the container was removed from the furnace and slowly cooled to room temperature. Finally, the presence of borides formed on the surface of AISI 1040 and AISI D2 steels were confirmed by Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS) and X-Ray Diffraction (XRD) techniques. Figure 1 shows (SEM) images of boron deposited on the surface of AISI D2 and AISI 1040 steels, the XRD scans (Figure 2) of the borided samples confirmed the presence of a single FeB phase formed in the D2 steel at 1220 K (Fig. 2a) and 1320 K (Fig. 2c). A double phase borided layer FeB+Fe2B was confirmed by XRD in the AISI 1040 samples treated at 1220 K (Fig. 2b) and 1320 K (Fig. 2d). Fe2B layers has a columnar morphology and dense structure. The depth of borides formed on AISI D2 is lower than that of AISI 1040 as expected. The chemical composition of borided samples are given in Table 1 showing that all samples contain deposited boron on its surface. These results demonstrate that the process of boron powder-pack applied to AISI 1040 and AISI D2 steels form...
A study of the initial states during the postdicharge nitriding process by microwave is set. In this process unlike the process of nitriding for ammonium gas, where the process of dissociation of the molecule involves reacting NH3 catalytic surface of the iron piece, the excitation of the nitrogen molecule is performed by collision between an electron and N2 molecule generating the reactive species with vibrational levels under 45, described by the following expression: N2 (X, υ ≤ 45 ), [1].The active neutral species generated in the discharge and transported to the piece developed a concentration gradient from the surface. The adsorption process generated by physisorption and chemisorption in the substrate develop an initial concentration profile [2-4] and for long treatment time, results in the development of compact layers.In particular, in the postdischarge nitriding process, the production of neutral active species and the transport of mass into the solid are related to kinetics reaction that leads to the very rapid precipitation of nitrides in the surface.Specimens of ARMCO Iron (200 mm diameter; Mn, 880 ppm; C and P, 220 ppm; 0.23 Si, S, 150 ppm) were nitrided during short period of times. The sample surface to be exposed was polished down to 3 μm and thoroughly cleaned in an acetone ultrasonic bath before nitriding. Nitriding experiments were carried out in a post-discharge flow of plasma generated in the microwave reactor, which is described in previous works [5]. Figures 1(a-c) shows optical micrographs from the specimens treated by postdicharge nitriding process. Specimen treated for 5 seconds (fig 1a), 25 s. (fig. 1b) and 180 s. (fig. 1c) respectively. Fig. 1d shows a Scanning Electron Microscopy from the sample nitrided for 180 s. The X-ray diffraction ( fig. 2) spectra shows that the formation of the '-Fe4N on the top of the surface occurs at short treatment time. On other hand, the intensity of theFe4N diffraction lines increases with respect to time of treatment.
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