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In consequence of the escalating utilization of hydrogenation catalysts in petroleum, one of the world's three primary energy sources, there has been a concomitant increase in the quantity of deactivated spent catalysts. As a hazardous waste material that poses a threat to human health and environmental safety, the recovery of valuable metals from these catalysts presents an environmentally friendly approach that aligns with the principles of a circular economy. The present study focuses on the efficient utilization of spent hydrogenation catalysts. To this end, it summarizes pretreatment processes, leaching methods, separation and purification techniques, and high-value-added utilization strategies. By evaluating the recovery principles and efficiencies of various methods within each process, the advantages and disadvantages of different approaches are delineated. It is evident that solvent extraction demonstrates considerable promise in the context of pretreatment processes, owing to its simplicity, high efficiency in oil removal, and recyclability. The roasting-leaching method has been shown to achieve higher leaching rates during the leaching process. In the domains of separation and purification, solvent extraction offers distinct advantages, including its high selectivity and mild operating conditions. In comparison with metallurgical methods, the regeneration and reuse processes in high-value-added utilization are shorter and more economically beneficial, particularly when utilizing spent catalysts as raw materials for the production. This approach achieves a balance between economic and environmental considerations, although it should be noted that the technology is not yet fully mature. In addition to the aforementioned points, this paper proposes targeted strategies for the challenges faced in the recycling of spent hydrogenation catalysts. The aim of this paper is to provide a reference for the industrialization of spent catalyst recycling.
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http://dx.doi.org/10.1021/acs.est.5c04246 | DOI Listing |
Inorg Chem
September 2025
College of Chemistry and Materials Science, The key Laboratory of Functional Molecular Solids, Ministry of Education, The Key Laboratory of Electrochemical Clean Energy of Anhui Higher Education Institutes, Anhui Provincial Engineering Laboratory for New-Energy Vehicle Battery Energy-Storage Materia
Conventional acid-catalyzed acetalization faces significant challenges in catalyst recovery and poses environmental concerns. Herein, we develop a CeO-supported Pd single-atom catalyst (Pd/CeO) that eliminates the reliance on liquid acids by creating a localized H-rich microenvironment through heterolytic H activation. X-ray absorption near-edge structure and extended X-ray absorption fine structure analyses confirm the atomic dispersion of Pd via Pd-O-Ce coordination, while density functional theory (DFT) calculations reveal strong metal-support interactions (SMSI) that facilitate electron transfer from CeO oxygen to Pd, downshifting the Pd d-band center and optimizing H activation.
View Article and Find Full Text PDFAdv Mater
September 2025
College of Chemistry, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, P. R. China.
Formic acid (FA) has attracted significant interest as a renewable liquid-phase hydrogen carrier. Hydrogen generation from FA decomposition is essential for the development of hydrogen economy. Designing highly efficient catalysts with different coordination environments for FA dehydrogenation is crucial for fuel-cell applications.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing 211189, China.
Developing efficient and durable catalysts for the oxygen evolution reaction (OER) in acidic media is essential for advancing proton exchange membrane water electrolysis (PEMWE). However, catalyst instability caused by lattice oxygen (O) depletion and metal dissolution remains a critical barrier. Here, we propose an oxophilic-site-mediated dynamic oxygen replenishment mechanism (DORM), in which O actively participates in O-O bond formation and is continuously refilled by water-derived species.
View Article and Find Full Text PDFNanoscale Adv
August 2025
School of Electronic Science, Odisha University of Technology and Research Bhubaneswar India.
A novel electrocatalyst, zirconium ferrite nanoparticles (NPs) (ZrFeO NPs), was synthesized through coprecipitation and calcination processes at 300 °C and 500 °C using iron rust. The ZrFeO NPs were used as catalysts for the hydrogen evolution reaction. Furthermore, these NPs in an alkaline medium exhibited superior properties of a fractional order supercapacitor, based on which a prototype device was fabricated to demonstrate its energy storage applications.
View Article and Find Full Text PDFACS Omega
September 2025
International Centre for Materials Science, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur- P.O., Bangalore 560064, India.
Lambert and co-workers have developed several chiral bases using a cyclopropeneimine as the basic moiety. Typically, these catalysts have a pendant hydroxyl group which acts as a hydrogen-bond donor and activates the electrophile. In catalysts with a hydrogen-bond donor, prior work from the Sigman group has shown that the acidity of the donor plays an important role in imparting selectivity.
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