28 research outputs found

    Trends and perspectives in the use of organic acids for critical metal recycling from hard-metal scraps

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    Hard-metal sector, strategic for the industrial economies, is suffering from the reduced availability and price volatility of its main feedstock: critical W and Co. In 2021, a 73.5 kt W and 9.2 kt Co demand for hard-metal production (65% and 5.3% of global demand, respectively), was recorded. Hard-metal scrap recycling is hence desirable for both environmental and economic reasons. A significant recovery of W and Co from manufacturing by-products and scraps is already good practice in the hard-metal industry (42% for W and 22% for Co). However, there is still a lot to do to meet the technical-economic-environmental sustainability in materials and energy enhancement for pursuing a green economy model. Indeed, Chemical Modification and Direct Recycling, which are the most widely employed industrial approaches, typically involve energy and/or harsh chemicals-intensive treatments which require expensive equipment and skilled workers. In the last decade, research efforts have been spent on implementing alternative materials reclamation processes from hard-metal scraps based on the use of bio-based organic acids with the view to increase the rate and quality of the recycled materials exploiting their peculiar metal complexing action as well as to preserve natural resources and prevent the disposal of potentially toxic/polluting substances. Despite the preliminary stage of the research, organic acids were demonstrated to be powerful but gentle agents for the selective leaching of cobalt from WC-Co-based materials as well as promising agents for WO3 dissolution. Indeed, thanks to their acid and complexing properties, they can stabilize metals in their oxidized form giving soluble products and preventing passivation phenomena. Furthermore, organic acids can be obtained by renewable biomass transformation, limiting the request for high-impact industrial chemicals. Hence they points out key features making them promising for the design of eco-friendly recovery processes. In this context, the different industrial approaches to the recovery and recycling of Hard-metal wastes, with specific reference to the role of bio-derived organic acids in hydro- and solvo-metallurgical processes, will be critically reviewed with the view of opening a discussion on the perspectives of their use in designing circular economy models in HM manufacturing as economically, technically and environmentally sustainable as possible

    A comparison among bio-derived acids as selective eco-friendly leaching agents for cobalt: the case study of hard-metal waste enhancement

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    Peculiar chemical, mechanical, and magnetic properties make cobalt a key metal for a variety of “hot” applications like the cathode production of Li-ion batteries. Cobalt is also the preferred metallic binder for tungsten carbide tool manufacturing. The recent increasing criticality of cobalt and tungsten is driving the interest of manufacturers and researchers toward high-rate recycling of hard-metal (HM) waste for limiting the demand for raw materials. A simple and environmentally friendly hydrometallurgical route for Co-selective dissolution from HM wastes was developed by using weak, bio-derived, and biodegradable organic acids (OAs). In this study, OAs, namely, acetic (HAc), citric (H3Cit), maleic (H2Mal), lactic (HLac), succinic (H2Suc), lactobionic (HLB), and itaconic (H2It) acids, were selected for their pKa1 values spanning from 1.8 to 4.7 and systematically tested as selective cobalt leaching agents from WC-Co-based wastes in water, isolating the formed complexes in the solid state. Thereby, all of them seemed to be efficient in selective Co leaching, achieving almost quantitative Co dissolution from HM by-products still at low concentration levels and room conditions in a short time, leaving the residual WC unreacted and ready to be re-employed for industrial purposes. Nevertheless, two main categories of organic acids were distinguished depending on their oxidizing/complexing behavior: class 1 OAs, where the metal oxidation is carried out by H+, and class 2 OAs, where oxidation is carried out by an external oxidant like O2. A combined experimental/theoretical investigation is described here to show the reasons behind this peculiar behavior and lay the foundation for a wider discussion on the leaching capabilities of OAs toward elemental metals. Due to the demonstrated effectiveness, low cost, eco-friendliness, and large availability through biotechnological fermentative processes, particular attention is devoted here to the use of HLac in hydrometallurgy as an example of class 2 OA. WC-Co materials recovered by HLac mild hydrometallurgy demonstrated a metallurgical quality suitable for re-employment in the HM manufacturing process

    A new facile solvometallurgical leaching method for the selective Co dissolution & recovery from hard metals waste

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    Hard Metals (HM) production plays a fundamental role in economy and technological development. Due to the criticality of its main raw materials, W and Co, a sustainable HM waste recycling is hence desirable for both environmental and economic reasons and strongly encouraged by European waste management directives. This work describes a new solvometallurgical leaching method based on diluted maleic acid (H2Mal) ethanolic solutions, which demonstrated to couple effectiveness in materials enhancement from HM waste, with mildness and sustainability of operative conditions. Specifically, H2Mal (0.5 M, EtOH) selectively and quantitatively leached Co trapped within WC-Co powders, to afford [Co(HMal)2(H2O)4] complex within 4 h at room temperature and leaving WC unreacted and ready for re-employment in HM manufacturing. Characterization of the resultant materials i.e. treated powders (SEM-EDS, p-XRD, ICP-OES) and Co-leaching solutions (ICP-OES), confirmed the near quantitative Co removal as well as the possibility to finely tune the composition of WC-Co mixtures. Parameters for best leaching conditions, i.e. time and liquid-to-solid ratio, were obtained. A scale-up experiment addressed to test the leaching conditions and the quality of the recycled material is also described. The quality of the recycled material for direct re-employment in HM manufacturing was validated by Metallurgical Quality Control, to good effect. Finally, preliminary experiments on cobalt metal recovery from the metal complex by electrowinning and by quantitative precipitation as CoCO3 were performed with encouraging results: a step forward resources circularity

    Corrosion of cemented carbide grades in petrochemical slurries. Part I - Electrochemical adsorption of CN¯, SCN¯ and MBT: A study based on in situ SFG

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    Owing to their unique combination of wear resistance and toughness, cemented carbides are developing relevance in a systematically increasing number of applications, many of which involve notably corrosive environments. Petrochemical offshore extraction is one of the most appealing prospective fields of use of cemented carbides for critical general-purpose components (e.g. pumps and valves), as well as specialised devices, such as drilling mud circulation systems, as they undergo extremely severe erosion-corrosion related to the handling of tetraphasic flows comprising condensed and gas-phase hydrocarbons in addition to sand or other solid components of slurries. Moreover, oilfields of current interest bear high concentrations of strongly corrosive impurities. The present study is aimed at contributing to the knowledge of the corrosion and corrosion inhibition processes of a range of alloyed Co- and Ni-based cemented carbide grades in solutions containing cyanide (CN¯) and thiocyanate (SCN¯) - typical corrosive contaminants found in crude oil - and 2-mercaptobenzothiazole (MBT), a prospective corrosion inhibitor in the petrochemical field. To this aim, we employed: (i) linear sweep voltammetry (LSV) to assess the cathodic and anodic activity of the hardmetal grades; (ii) in situ Sum- Frequency Generation (SFG) spectroscopy as a sensitive probe of the potential-dependent interfacial chemistry and corrosion behaviour in terms of both adsorption and interaction of adsorbates with the electronic structure of the substrate; (iii) ex situ spectro-ellipsometry to characterise the films formed on the different grades in the investigated environments.We have found that: (i) the grade with Co‐Ru binder exhibits a generally better corrosion resistance in all investigated ambients; (ii) Ni affords protective action provided the oxidising power is below a given threshold and CN¯ is absent, and (iii) MBT improves the pseudopassivation of all the investigated cemented carbides. Typical potential-dependent SFG spectral scenarios have been pinpointed for the different electrode/electrolyte combinations, accurately matching the electrochemical behaviour assessed by LSV and the optical properties of the corroded surfaces investigated by spectro-ellipsometry. This multi-method study offers a comprehensive and insightful understanding of the corrosion of cemented carbides in contact with additive-containing solutions

    Corrosion Behaviour of Cemented Carbides with Co- and Ni-Alloy Binders in the Presence of Abrasion

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    More and more often, cemented carbides are employed for the production of wear resistant components and have to face highly demanding service conditions that combine different damage mechanisms. A key example is the range of tetraphasic (sea water, sand, liquid and gaseous hydrocarbons) flows encountered in the Oil and Gas extraction industry. Notwithstanding the importance of operating regimes of this type, the availability of fundamental and quantitative information on the corrosion performance of cemented carbides in the presence of abrasion is still limited. In this paper, we report a systematic study of the corrosion behaviour of cemented tungsten carbide grades with binders containing different amounts of cobalt (Co), nickel (Ni), chromium (Cr) and noble metal additions, subjected to controlled mechanical abrasion, impacting the stability and nature of pseudopassivation films. In this work, special attention is devoted to Cr, a classical of additive that inhibits the Ostwald ripening of tungsten carbide (WC) particles and notably improves the corrosion resistance of grades with ultrafine-to-fine WC grain size and low-to-medium binder content. We assessed the impact of binder composition on the anodic behaviour by means of linear-sweep voltammetry and chronopotentiometry as well as on the mechanical properties. The application of controlled abrasion conditions under electrochemical control is carried out with an in-house modified ASTM B611 apparatus, equipped with a three-electrode system, enabling the systematic investigation of the synergy of electrochemical and mechanical damaging conditions. Increased corrosion resistance in environments without and with added chloride—both in the absence and in the presence of abrasion—was observed in all the Co- and Ni-based grades to which growing quantities of Cr were added. Moreover, doping with ruthenium (Ru) further enhances corrosion resistance. Regarding corrosion in the presence of abrasion, the addition of Cr and Ru increases the ability of regenerating the pseudopassivation film. The optimized compositions of the binder have been highlighted that open up attractive opportunities of improved service behaviour and deployment in new applications

    Effect of printing parameters on sintered WC-Co components by binder jetting

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    Hardmetals are materials employed to produce cutting and forming tools as well as wear resistant parts. Standard powder metallurgy suffers limitations in the manufacturing of shapes required by application-oriented design. Therefore, there is interest for the implementation of additive manufacturing, in particular low temperature techniques as binder jetting because they allow to preserve microstructures and peculiar properties. In our work, the powder was tungsten carbide with 12 wt.% cobalt (WC-Co). Shaping by binder jetting was followed by curing treatment to promote the binder polymerization, vacuum sintering and sinter-HIP to achieve near-full density. The powder was analysed in terms of size and shape, to determine its suitability for the procedure. Then, the effects of different combinations of printing parameters, layer thickness (50–100 μm) and binder saturation (60/75/90%), on the density of the green bodies were analysed. Finally, the relative density of the sintered components was measured and the pores shape and size were studied by SEM imaging, to assess possible consequences of the deposition procedure. Vickers hardness along the samples cross-section was measured and correlated to the printing conditions employed

    An SFG and DFG investigation of Au(111), Au(100), Au(110) and Au(210) electrodes in contact with aqueous solutions containing KCN

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    International audienceIn this paper, the behaviour of Au(111), (100), (110) and (210) electrodes in contact with pH-neutral aqueous solutions of KCN has been studied as a function of potential by means of in situ sum frequency generation (SFG) and difference frequency generation (DFG) spectros-copies. The contribution of both free and bound electrons has been included. Spectroelectrochemical results were complemented with cyclic voltammetric measurements. The main emphasis in this work has been placed on systematising and quantifying the interaction between the vibrational and electronic structures of the electrodic interfaces studied by the systematic comparison of SFG and DFG spectra measured under the same electrochemical conditions for different crystal orientations
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