The production of new automotive catalytic converters requires the increase of the quantity of Platinum Group Metals in order to deal with the strict emission standards that are imposed for vehicles. The use of PGMs coming from the recycling of spent autocatalysts could greatly reduce the cost of catalyst production for the automotive industry. This paper presents the synthesis of novel automotive Three-Way Catalysts (PLTWC, Pd/Rh = 55/5, 60 gPGMs/ft3) and diesel oxidation catalysts (PLDOC, Pt/Pd = 3/1, 110 gPGMs/ft3) from recovered PGMs, without further refinement steps. The catalysts were characterized and evaluated in terms of activity in comparison with benchmark catalysts produced using commercial metal precursors. The small-scale catalytic monoliths were successfully synthesized as evidenced by the characterization of the samples with XRF analysis, optical microscopy, and N2 physisorption. Hydrothermal ageing of the catalysts was performed and led to a significant decrease of the specific surface area of all catalysts (recycled and benchmarks) due to sintering of the support material and metal particles. The TWCs were studied for their activity in CO and unburned hydrocarbon oxidation reactions under a slightly lean environment of the gas mixture (λ > 1) as well as for their ability to reduce NOx under a slightly rich gas mixture (λ < 1). Recycled TWC fresh catalyst presented the best performance amongst the catalysts studied for the abatement of all pollutant gases, and they also showed the highest Oxygen Storage Capacity value. Moreover, comparing the aged samples, the catalyst produced from recycled PGMs presented higher activity than the one synthesized with the use of commercial PGM metal precursors. The results obtained for the DOC catalysts showed that the aged PLDOC catalyst outperformed both the fresh catalyst and the aged DOC catalyst prepared with the use of commercial metal precursors for the oxidation of CO, hydrocarbons, and NO. The latter reveals the effect of the presence of several impurities in the recovered PGMs solutions.
The increase in energy demands for the establishment of a modern digital era has resulted in the significant limitation of the energy sources. The depletion of energy reserves drew attention to alterative renewable energy sources that can satisfy the energy requirements in an environmentally friendly way. Hydrogen is an ideal chemical energy storage. Proton exchange membrane water electrolysis (PEMWE) is a promising technology as a green source of high-purity hydrogen. For that reason, PEMWE devices are already used in aerospace to produce oxygen for the crew on the Space Stations. The use of Critical Raw Materials (CRMs, especially Pt and Ir) and high cost materials in the PEMWE systems compromises their economic feasibility. It is necessary to implement End-of-Life (EoL) strategies that optimise the recovery of CRMs within feasible and environmentally friendly processes. In this paper an overview of the existing technologies for recycling of Membrane Electrode Assembles and electrocatalysts from PEMWE systems are revealed. MONOLITHOS has developed a novel optimized hydrometallurgical method for high PGMs recovery from spent automotive catalysts. This work aims to describe how this method can be applied to the EoL phase of PEMWE to improve techno-environmental and techno-economical performance of CRMs recovery.
The current study is focused on platinum recovery from the secondary sources of end-of-life heavy-duty diesel oxidation catalysts (DOCs) and heavy-duty catalyzed diesel particulate filters (c-DPFs) in order to reduce the supply–demand gap within the European Union. The extraction of platinum was based on a hydrometallurgical single-step low acidity leaching system (HCl-H2O2-NaCl) and a calcination step that takes place before the leaching process. The parameters of calcination and leaching process were thoroughly investigated in order to optimize recovery efficiency. The optimized results proved that a calcination step (at 800 °C for 2 h) improves the recovery efficiency by a factor of 40%. In addition, optimal Pt recovery yield was achieved after 3 h of leaching at 70 °C, with a solid-to-liquid (S/L) ratio of 70 g/100 mL (70%) and 3 M HCl-1% vol H2O2-4.5 M NaCl as leaching conditions. The optimum Pt recovery yield was 95% and 75% for DOC and c-DPF, respectively. Since the secondary feedstock investigated is highly concentrated in platinum, the pregnant solution can be used as a precursor for developing new Pt-based catalytic systems.
PROMETHEUS catalyst, a copper-based polymetallic nano-catalyst has been proven to be suitable for automotive emission control applications. This novel catalyst consists of copper, palladium and rhodium nanoparticles as active phases, impregnated on an inorganic oxide substrate, CeO2/ZrO2 (75%, 25%). The aim of PROMETHEUS catalyst’s development is the substitution of a significant amount (85%) of Platinum Group Metals (PGMs) with copper nanoparticles while, at the same time, presenting high catalytic efficiency with respect to the commercial catalysts. In this work, an extensive investigation of the catalytic activity of full scale PROMETHEUS fresh and aged catalyst deposited on ceramic cordierites is presented and discussed. The catalytic activity was tested on an Synthetic Gas Bench (SGB) towards the oxidation of CO and CH4 and the reduction of NO. The loading of the washcoat was 2 wt% (metal content) on Cu, Pd, Rh with the corresponding metal ratio at 21:7:1. The concentration of the full-scale monolithic catalysts to be 0.032% total PGM loading for meeting Euro III standard and 0.089% for meeting Euro IV to Euro VIb standards. The catalytic activity of all catalysts was tested both in rich-burn (λ = 0.99) and lean-burn conditions (λ = 1.03).
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