Preparation and characterization of Ti–Ta alloys for application in corrosive media
Introduction
Pure titanium (Ti) offers outstanding corrosion resistance in a wide variety of environments, specially oxidizing, neutral and inhibited reducing media [1]. The corrosion resistance of Ti is due to the formation of a protective and self-adherent oxide film mainly composed of TiO2 [2]. For this reason, Ti is widely used for handling nitric acid in industrial applications and marine environments [3]. Nevertheless, Ti is severely attacked in reducing acids [1], except when oxidizing species such as oxygen, ferric, cupric and chromic ions are present [4].
Tantalum (Ta) exhibits an excellent corrosion resistance in almost all aqueous media except HF and alkaline solutions [5]. Its main application is found in equipments for chemical industry dealing with hot and concentrated mineral-reducing acids such as H2SO4 e HCl, where the usual structural alloys do not resist [6], [7]. Its high resistance is due to the formation of a protective Ta2O5 oxide film. It is not more widely used in chemical environments due to its high cost, nearly 10 and 5 times the cost of stainless steel and Ti for finished fabricated equipment, respectively [8].
Ti–Ta alloys are promising materials for substitution of Ta because they save weight and cost when compared to Ta and are expected to present higher corrosion resistance than Ti in reducing acids. Despite these advantages, few works are available about Ti–Ta alloys and their corrosion resistance [9], [10], [11]. Especially, no data are available on their electrochemical behavior in reducing acid solutions.
In this work, Ti-20, 40, 60 and 80 wt.% Ta alloys were obtained by arc melting, with and without subsequent heat treatment, and characterized using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and X-ray diffractometry (XRD). The microhardness and density of the alloys were also measured. Some preliminary electrochemical experiments were performed to evaluate the corrosion behavior of the Ti–Ta alloys in 80 wt.% H2SO4 solutions at room temperature.
Section snippets
Experimental procedure
Ti and Ta shapes were mixed in the appropriate proportions to obtain the Ti-20, 40, 60 and 80 wt.% Ta alloys. The pure metals were previously degreased and pickled in 4HNO3+1HF (v/v) solution for Ti and 2HNO3+2HF+5H2SO4+2H2O (v/v) solution for Ta. The mixtures were arc melted under argon atmosphere of 99.9% purity. After the first melting, samples were cut from the ingots, mounted in resin, grounded until 4000 grit and polished using an aqueous suspension of Al2O3 powder. The remaining
Preparation and characterization of the Ti–Ta alloys
After the first melting, two important observations were made from MEV observations: (1) an incomplete fusion of the Ta shapes occurred and (2) a great segregation took place during solidification. Difficulties for the obtainment of Ti–Ta alloys by conventional arc melting have been reported [12]. These difficulties arise from the great difference between the melting point and density of both Ti and Ta (Table 1) and the relatively large two-phase (liquid+solid) field in the binary Ti–Ta phase
Conclusions
The Ti-20, 40, 60 and 80 wt.% Ta alloys were produced by arc melting followed by heat treatment at 1200 °C for 48 h and cooling to room temperature in the furnace.
Both α- and β-phases were detected in the microstructure of Ti–20Ta and Ti–40Ta alloys, whereas only the β-phase was present in Ti–60Ta and Ti–80Ta alloys.
The microhardness of these alloys was higher than those of Ti and Ta.
From a preliminary electrochemical study in 80 wt.% H2SO4 solutions at room temperature, Ti–20Ta was shown to be
Acknowledgments
K.A.S. and A.R. acknowledge the Fundação de Amparo à Pesquisa do Estado de São Paulo—Brazil (FAPESP) for financial support (proc. 01/06974-0 and 00/13707-5).
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