## Abstract An in‐situ FT‐IR spectroelectrochemical and voltammetric study of the corrosion of a WC‐Co hardmetal grade is reported in this communication. A slightly acidic sulphate solution is considered. The potential‐ and time‐dependent anodic formation of CO~2~ and Co(OH)~2~ can be followed with
Anodic behaviour of WC-Co type hardmetal
✍ Scribed by B. Bozzini; G. P. De Gaudenzi; A. Fanigliulo; C. Mele
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- German
- Weight
- 670 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0947-5117
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✦ Synopsis
Abstract
An understanding of the anodic behaviour of WC‐Co type hardmetals is vital for the functional behaviour of this class of materials. The anodic oxidation of WC‐13Co grade hardmetal in 0.1 M H~2~SO~4~ was investigated. This study is based on electrochemical (linear sweep voltammetry, cyclic voltammetry, impedance spectroscopy), compositional (energy dispersive spectroscopy), structural (X‐ray diffraction) and morphological (scanning electron microscopy) investigations. The potential range in which the oxidation of the Co‐alloy takes place with respect to the nobler carbide phase was defined. Within this potential interval a passivating behaviour for the binder alloy was shown. The potential threshold for WC oxidation was identified by monitoring the inception of the electrochromic loop. The anodic attack gives rise to the formation of hydrous WO~3~. The attack morphology is characterised by the alteration of the grain shape with formation of jelly‐like microscopic and flaky macroscopic structures.
📜 SIMILAR VOLUMES
The electrodes prepared from the sintered tungsten carbide (WC) containing 10 vol.% of nickel or cobalt or iron, with Vickers hardness > 1200 kg mm-\*, were anodically polarized in 5 x 10-r mol dm-r aqueous solution of sulphuric acid. Material from the electrodes was electrochemically studied after
Stationary electrodes prepared from the sintered tungsten carbide (WC, M) containing 10 ~01% of M = Co, Ni or Fe binder, with Vickers hardness > 1200 kg mm-', have been investigated in 0.5 M H,SO, using the Scanning Electron Microscopy (SEM) and the Electrochemical Impedance Spectroscopy (EIS) metho