With the undergoing unprecedented development of lithium-ion batteries (LIBs), the recycling of end-of-life batteries has become an urgent task considering the demand for critical materials, environmental pollution, and ecological impacts. Selective recovery of targeted element(s) is becoming a topical field that enables metal recycling in a short path with highly improved material efficiencies. This research demonstrates a process of selective recovery of spent Ni-Co-Mn (NCM)-based lithium-ion battery by systematically understanding the conversion mechanisms and controlling the sulfur behavior during a modified-sulfation roasting. As a result, Li from complex cathode components can be selectively extracted with high efficiency by only using water. Notably, the sulfur driven recovery processes can be divided into two stages: (i) part of the structure of NCM523 was destroyed, and Ni, Co, and Mn were reduced to divalent in different degrees to form sulfate (NiSO, CoSO, MnSO) when reacting with HSO at ambient temperature; (ii) with increasing temperature, Li ions in the unstable layered structure are released and combined with SO in the transition metal sulfate to form LiSO, and the sulfates of transition metals react to form NiCoMnO. Studies have shown sulfur can be recirculated thoroughly in the form of SO, which in principle avoids secondary pollutions. By controlling the appropriate conversion temperature, we envisage that the sulfation selective roasting recovery technology could be easily applied to other spent lithium-ion battery materials. Besides, this work may also provide a unique platform for further study on the efficient extracting of other mineral resources.
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http://dx.doi.org/10.1021/acsami.0c00420 | DOI Listing |
ACS Omega
January 2025
Biotechnology Research Center and Department of Biotechnology, Toyama Prefectural University, 5180 Kurokawa, Imizu, Toyama 939-0398, Japan.
Various symmetric and asymmetric imines were synthesized using the novel amine oxidase, obtained as variants of d-amino acid oxidase (pkDAO) from porcine kidney (Y228L/R283G) and (I230A/R283G). Active primary imines produced as intermediates in the oxidation of methylbenzylamine (MBA) derivatives were trapped by aliphatic, aromatic amines and diamines as nucleophiles forming new imines. ()-Fluoro-MBA was the best substrate for symmetric imine synthesis, providing almost stoichiometric conversion (100 mM) and achieving nearly 100% yield.
View Article and Find Full Text PDFChem Soc Rev
January 2025
Birmingham Centre for Energy Storage & School of Chemical Engineering, University of Birmingham, UK.
This review explores the behavior of low-concentration CO (LCC) in various energy media, such as solid adsorbents, liquid absorbents, and catalytic surfaces. It delves into the mechanisms of diffusion, adsorption, and catalytic reactions, while analyzing the potential applications and challenges of these properties in technologies like air separation, compressed gas energy storage, and CO catalytic conversion. Given the current lack of comprehensive analyses, especially those encompassing multiscale studies of LCC behavior, this review aims to provide a theoretical foundation and data support for optimizing CO capture, storage, and conversion technologies, as well as guidance for the development and application of new materials.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Karlsruhe Institute of Technology KIT, Institute for Chemical Technology and Polymer Chemistry, Kaiserstr. 12, Fakultät für Chemie, 76131, Karlsruhe, GERMANY.
In the frame of developing a sustainable chemical industry, heterogeneously catalyzed CO2 hydrogenation to methanol has attracted considerable interest. However, the Cu-Zn based catalyst system employed in this process is very dynamic, especially in the presence of the products methanol and water. Deactivation needs to be prevented, but its origin and mechanism are hardly investigated at high conversion where product condensation is possible.
View Article and Find Full Text PDFSmall
January 2025
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, 68 Jincheng Street, Wuhan, Hubei, 430078, P. R. China.
Hydrogen peroxide (HO) production through photocatalytic O reduction reaction (ORR) is a mild and cost-efficient alternative to the anthraquinone oxidation strategy. Of note, singlet state oxygen (O) plays a crucial role in ORR. Herein, a hollow TiO@TpPa (TOTP) S-scheme heterojunction by the Schiff base reactions involving 1,3,5-triformylphloroglucinol (Tp) and paraphenylenediamine (Pa) for efficient photocatalytic HO production in deionized water has been developed.
View Article and Find Full Text PDFSmall Methods
January 2025
Center for Photonics Information and Energy Materials, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong, 518055, P. R. China.
Wide-bandgap perovskite solar cells (PVSCs), a promising top-cell candidate for high-performance tandem solar cells, often suffer from larger open-circuit voltage (V) deficits as the bandgap increases. Surface passivation is a common strategy to mitigate these V deficits. However, understanding the mechanisms underlying the differences in passivation effects among various types of molecules remains limited, which is crucial for developing universal interface passivation strategies and guiding the design of passivation molecules.
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