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Search Results (12)

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Keywords = rare-earth metal catalysis

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5 pages, 1127 KiB  
Proceeding Paper
The Synthesis of the System SiO2-Gd2O3-Eu2O3 and Research on the Acid-Base Properties and Kinetics of Particle Formation in This System
by Sabukhi I. Niftaliev, Irina V. Kuznetsova and Nhat Anh Tran
Mater. Proc. 2025, 21(1), 2; https://doi.org/10.3390/materproc2025021002 - 13 Feb 2025
Viewed by 686
Abstract
This study investigates the synthesis and characterization of SiO2-Gd2O3-Eu2O3 nanomaterials. The sol–gel method was employed using tetraethoxysilane (TEOS), gadolinium nitrate, and europium nitrate as precursors. The influence of rare earth oxide concentration on the [...] Read more.
This study investigates the synthesis and characterization of SiO2-Gd2O3-Eu2O3 nanomaterials. The sol–gel method was employed using tetraethoxysilane (TEOS), gadolinium nitrate, and europium nitrate as precursors. The influence of rare earth oxide concentration on the hydrolysis kinetics and activation energy was evaluated. Additionally, the acid-base properties of the synthesized materials were examined using the Hammett indicator adsorption method. The results revealed that the addition of Gd2O3 and Eu2O3 oxides to the system accelerated the hydrolysis process and reduced the activation energy. The formation of a layered structure, consisting of a central Si(OH)4 nucleus, a Si-O-Si polymer layer, and hydrated metal ion layers, was observed. The acid-base properties of the synthesized nanomaterials were influenced by the drying method and the composition of the system. The findings provide valuable insights into the synthesis and properties of SiO2-Gd2O3-Eu2O3 nanomaterials, which have potential applications in various fields such as optoelectronics and catalysis. Full article
(This article belongs to the Proceedings of The International Conference on Advanced Nano Materials)
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31 pages, 7418 KiB  
Review
Rare Earths—The Answer to Everything
by Thomas Behrsing, Victoria L. Blair, Florian Jaroschik, Glen B. Deacon and Peter C. Junk
Molecules 2024, 29(3), 688; https://doi.org/10.3390/molecules29030688 - 1 Feb 2024
Cited by 16 | Viewed by 14751
Abstract
Rare earths, scandium, yttrium, and the fifteen lanthanoids from lanthanum to lutetium, are classified as critical metals because of their ubiquity in daily life. They are present in magnets in cars, especially electric cars; green electricity generating systems and computers; in steel manufacturing; [...] Read more.
Rare earths, scandium, yttrium, and the fifteen lanthanoids from lanthanum to lutetium, are classified as critical metals because of their ubiquity in daily life. They are present in magnets in cars, especially electric cars; green electricity generating systems and computers; in steel manufacturing; in glass and light emission materials especially for safety lighting and lasers; in exhaust emission catalysts and supports; catalysts in artificial rubber production; in agriculture and animal husbandry; in health and especially cancer diagnosis and treatment; and in a variety of materials and electronic products essential to modern living. They have the potential to replace toxic chromates for corrosion inhibition, in magnetic refrigeration, a variety of new materials, and their role in agriculture may expand. This review examines their role in sustainability, the environment, recycling, corrosion inhibition, crop production, animal feedstocks, catalysis, health, and materials, as well as considering future uses. Full article
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25 pages, 3069 KiB  
Review
From E-Waste to High-Value Materials: Sustainable Synthesis of Metal, Metal Oxide, and MOF Nanoparticles from Waste Printed Circuit Boards
by Tatiana Pineda-Vásquez, Leidy Rendón-Castrillón, Margarita Ramírez-Carmona and Carlos Ocampo-López
Nanomaterials 2024, 14(1), 69; https://doi.org/10.3390/nano14010069 - 26 Dec 2023
Cited by 10 | Viewed by 5446
Abstract
The exponential growth of electronic waste (e-waste) has raised significant environmental concerns, with projections indicating a surge to 74.7 million metric tons of e-waste generated by 2030. Waste printed circuit boards (WPCBs), constituting approximately 10% of all e-waste, are particularly intriguing due to [...] Read more.
The exponential growth of electronic waste (e-waste) has raised significant environmental concerns, with projections indicating a surge to 74.7 million metric tons of e-waste generated by 2030. Waste printed circuit boards (WPCBs), constituting approximately 10% of all e-waste, are particularly intriguing due to their high content of valuable metals and rare earth elements. However, the presence of hazardous elements necessitates sustainable recycling strategies. This review explores innovative approaches to sustainable metal nanoparticle synthesis from WPCBs. Efficient metal recovery from WPCBs begins with disassembly and the utilization of advanced equipment for optimal separation. Various pretreatment techniques, including selective leaching and magnetic separation, enhance metal recovery efficiency. Green recovery systems such as biohydrometallurgy offer eco-friendly alternatives, with high selectivity. Converting metal ions into nanoparticles involves concentration and transformation methods like chemical precipitation, electrowinning, and dialysis. These methods are vital for transforming recovered metal ions into valuable nanoparticles, promoting sustainable resource utilization and eco-friendly e-waste recycling. Sustainable green synthesis methods utilizing natural sources, including microorganisms and plants, are discussed, with a focus on their applications in producing well-defined nanoparticles. Nanoparticles derived from WPCBs find valuable applications in drug delivery, microelectronics, antimicrobial materials, environmental remediation, diagnostics, catalysis, agriculture, etc. They contribute to eco-friendly wastewater treatment, photocatalysis, protective coatings, and biomedicine. The important implications of this review lie in its identification of sustainable metal nanoparticle synthesis from WPCBs as a pivotal solution to e-waste environmental concerns, paving the way for eco-friendly recycling practices and the supply of valuable materials for diverse industrial applications. Full article
(This article belongs to the Special Issue Nanomaterials for Green and Sustainable World)
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10 pages, 5757 KiB  
Article
Surface-Modified In2O3 for High-Throughput Screening of Volatile Gas Sensors in Diesel and Gasoline
by Deqi Zhang, Shenghui Guo, Jiyun Gao, Li Yang, Ye Zhu, Yanjia Ma and Ming Hou
Materials 2023, 16(4), 1517; https://doi.org/10.3390/ma16041517 - 11 Feb 2023
Cited by 1 | Viewed by 1472
Abstract
In this paper, with the help of the method of composite materials science, parallel synthesis and high-throughput screening were used to prepare gas sensors with different molar ratios of rare earths and precious metals modified In2O3, which could be [...] Read more.
In this paper, with the help of the method of composite materials science, parallel synthesis and high-throughput screening were used to prepare gas sensors with different molar ratios of rare earths and precious metals modified In2O3, which could be used to monitor and warn the early leakage of gasoline and diesel. Through high-throughput screening, it is found that the effect of rare earth metal modification on gas sensitivity improvement is better than other metals, especially 0.5 mol% Gd modified In2O3 (Gd0.5In) gas sensor has a high response to 100 ppm gasoline (Ra/Rg = 6.1) and diesel (Ra/Rg = 5) volatiles at 250 °C. Compared with the existing literature, the sensor has low detection concentration and suitable stability. This is mainly due to the alteration of surface chemisorption oxygen caused by the catalysis and modification of rare earth itself. Full article
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50 pages, 15151 KiB  
Review
Key Features of TEMPO-Containing Polymers for Energy Storage and Catalytic Systems
by Anatoliy A. Vereshchagin, Arseniy Y. Kalnin, Alexey I. Volkov, Daniil A. Lukyanov and Oleg V. Levin
Energies 2022, 15(7), 2699; https://doi.org/10.3390/en15072699 - 6 Apr 2022
Cited by 17 | Viewed by 6051
Abstract
The need for environmentally benign portable energy storage drives research on organic batteries and catalytic systems. These systems are a promising replacement for commonly used energy storage devices that rely on limited resources such as lithium and rare earth metals. The redox-active TEMPO [...] Read more.
The need for environmentally benign portable energy storage drives research on organic batteries and catalytic systems. These systems are a promising replacement for commonly used energy storage devices that rely on limited resources such as lithium and rare earth metals. The redox-active TEMPO (2,2,6,6-tetramethylpiperidin-1-oxyl-4-yl) fragment is a popular component of organic systems, as its benefits include remarkable electrochemical performance and decent physical properties. TEMPO is also known to be an efficient catalyst for alcohol oxidation, oxygen reduction, and various complex organic reactions. It can be attached to various aliphatic and conductive polymers to form high-loading catalysis systems. The performance and efficiency of TEMPO-containing materials strongly depend on the molecular structure, and thus rational design of such compounds is vital for successful implementation. We discuss synthetic approaches for producing electroactive polymers based on conductive and non-conductive backbones with organic radical substituents, fundamental aspects of electrochemistry of such materials, and their application in energy storage devices, such as batteries, redox-flow cells, and electrocatalytic systems. We compare the performance of the materials with different architectures, providing an overview of diverse charge interactions for hybrid materials, and presenting promising research opportunities for the future of this area. Full article
(This article belongs to the Collection Review Papers in Energy and Environment)
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32 pages, 3769 KiB  
Review
An Insight into Geometries and Catalytic Applications of CeO2 from a DFT Outlook
by Hussein A. Miran, Zainab N. Jaf, Mohammednoor Altarawneh and Zhong-Tao Jiang
Molecules 2021, 26(21), 6485; https://doi.org/10.3390/molecules26216485 - 27 Oct 2021
Cited by 26 | Viewed by 5007
Abstract
Rare earth metal oxides (REMOs) have gained considerable attention in recent years owing to their distinctive properties and potential applications in electronic devices and catalysts. Particularly, cerium dioxide (CeO2), also known as ceria, has emerged as an interesting material in a [...] Read more.
Rare earth metal oxides (REMOs) have gained considerable attention in recent years owing to their distinctive properties and potential applications in electronic devices and catalysts. Particularly, cerium dioxide (CeO2), also known as ceria, has emerged as an interesting material in a wide variety of industrial, technological, and medical applications. Ceria can be synthesized with various morphologies, including rods, cubes, wires, tubes, and spheres. This comprehensive review offers valuable perceptions into the crystal structure, fundamental properties, and reaction mechanisms that govern the well-established surface-assisted reactions over ceria. The activity, selectivity, and stability of ceria, either as a stand-alone catalyst or as supports for other metals, are frequently ascribed to its strong interactions with the adsorbates and its facile redox cycle. Doping of ceria with transition metals is a common strategy to modify the characteristics and to fine-tune its reactive properties. DFT-derived chemical mechanisms are surveyed and presented in light of pertinent experimental findings. Finally, the effect of surface termination on catalysis by ceria is also highlighted. Full article
(This article belongs to the Special Issue Theoretical Aspects of Transition Metal Catalysis)
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15 pages, 5510 KiB  
Article
Towards the Circular Economy of Rare Earth Elements: Lanthanum Leaching from Spent FCC Catalyst by Acids
by Corradino Sposato, Enrico Catizzone, Alessandro Blasi, Marilena Forte, Assunta Romanelli, Massimo Morgana, Giacobbe Braccio, Girolamo Giordano and Massimo Migliori
Processes 2021, 9(8), 1369; https://doi.org/10.3390/pr9081369 - 5 Aug 2021
Cited by 11 | Viewed by 5321
Abstract
Rare earth elements (REEs) are strategic materials widely used in different applications from Information and Communication Technologies (ICT) to catalysis, which are expected to grow more in the future. In order to reduce the impact of market price and reduce the environmental effect [...] Read more.
Rare earth elements (REEs) are strategic materials widely used in different applications from Information and Communication Technologies (ICT) to catalysis, which are expected to grow more in the future. In order to reduce the impact of market price and reduce the environmental effect from soil extraction, recovery/purification strategies should be exploited. This paper presents a combined acid-leaching/oxalate precipitation process to recover lanthanum from spent FCC catalyst using nitric acid. Preferred to hydrochloric and sulphuric acid (preliminary assessed), HNO3 showed a good capability to completely leach lanthanum. The combination with an oxalate precipitation step allowed demonstrating that a highly pure (>98% w/w) lanthanum solid can be recovered, with a neglectable amount of poisoning metals (Ni, V) contained into the spent catalyst. This could open a reliable industrial perspective to recover and purify REE in the view of a sustainable recycling strategy. Full article
(This article belongs to the Special Issue Treatment and Utilization of Waste Materials)
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10 pages, 4381 KiB  
Perspective
Ionic Liquids Based on the Concept of Melting Point Lowering Due to Ethoxylation
by Manuel Rothe, Eva Müller, Patrick Denk and Werner Kunz
Molecules 2021, 26(13), 4034; https://doi.org/10.3390/molecules26134034 - 1 Jul 2021
Cited by 9 | Viewed by 3290
Abstract
Most of the commonly used Ionic Liquids (ILs) contain bulky organic cations with suitable anions. With our COMPLET (Concept of Melting Point Lowering due to Ethoxylation), we follow a different approach. We use simple, low-toxic, cheap, and commercially available anions of the type [...] Read more.
Most of the commonly used Ionic Liquids (ILs) contain bulky organic cations with suitable anions. With our COMPLET (Concept of Melting Point Lowering due to Ethoxylation), we follow a different approach. We use simple, low-toxic, cheap, and commercially available anions of the type Cx(EO)yCH2COO to liquefy presumably any simple metal ion, independently of its charge. In the simplest case, the cation can be sodium or lithium, but synthesis of Ionic Liquids is also possible with cations of higher valences such as transition or rare earth metals. Anions with longer alkyl chains are surface active and form surface active ionic liquids (SAILs), which combine properties of ionic and nonionic surfactants at room temperature. They show significant structuring even in their pure state, i.e., in the absence of water or any other added solvent. This approach offers new application domains that go far beyond the common real or hypothetical use of classical Ionic Liquids. Possible applications include the separation of rare earth metals, the use as interesting media for metal catalysis, or the synthesis of completely new materials (for example, in analogy to metal organic frameworks). Full article
(This article belongs to the Special Issue New Trends in Ionic Liquids Application)
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34 pages, 14929 KiB  
Review
Solvothermal Synthesis Routes to Substituted Cerium Dioxide Materials
by James W. Annis, Janet M. Fisher, David Thompsett and Richard I. Walton
Inorganics 2021, 9(6), 40; https://doi.org/10.3390/inorganics9060040 - 21 May 2021
Cited by 17 | Viewed by 6056
Abstract
We review the solution-based synthesis routes to cerium oxide materials where one or more elements are included in place of a proportion of the cerium, i.e., substitution of cerium is performed. The focus is on the solvothermal method, where reagents are heated above [...] Read more.
We review the solution-based synthesis routes to cerium oxide materials where one or more elements are included in place of a proportion of the cerium, i.e., substitution of cerium is performed. The focus is on the solvothermal method, where reagents are heated above the boiling point of the solvent to induce crystallisation directly from the solution. This yields unusual compositions with crystal morphology often on the nanoscale. Chemical elements from all parts of the periodic table are considered, from transition metals to main group elements and the rare earths, including isovalent and aliovalent cations, and surveyed using the literature published in the past ten years. We illustrate the versatility of this synthesis method to allow the formation of functional materials with applications in contemporary applications such as heterogeneous catalysis, electrodes for solid oxide fuel cells, photocatalysis, luminescence and biomedicine. We pick out emerging trends towards control of crystal habit by use of non-aqueous solvents and solution additives and identify challenges still remaining, including in detailed structural characterisation, the understanding of crystallisation mechanisms and the scale-up of synthesis. Full article
(This article belongs to the Special Issue Cornerstones in Contemporary Inorganic Chemistry)
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18 pages, 3029 KiB  
Article
C–H Bond Activation of Silyl-Substituted Pyridines with Bis(Phenolate)Yttrium Catalysts as a Facile Tool towards Hydroxyl-Terminated Michael-Type Polymers
by Thomas M. Pehl, Moritz Kränzlein, Friederike Adams, Andreas Schaffer and Bernhard Rieger
Catalysts 2020, 10(4), 448; https://doi.org/10.3390/catal10040448 - 22 Apr 2020
Cited by 7 | Viewed by 4328
Abstract
Herein, silicon-protected, ortho-methylated hydroxy-pyridines were reported as initiators in 2-aminoalkoxy-bis(phenolate)yttrium complexes for rare earth metal-mediated group-transfer polymerization (REM-GTP) of Michael-type monomers. To introduce these initiators, C−H bond activation was performed by reacting [(ONOO)tBuY(X)(thf)] (X = CH2TMS, thf [...] Read more.
Herein, silicon-protected, ortho-methylated hydroxy-pyridines were reported as initiators in 2-aminoalkoxy-bis(phenolate)yttrium complexes for rare earth metal-mediated group-transfer polymerization (REM-GTP) of Michael-type monomers. To introduce these initiators, C−H bond activation was performed by reacting [(ONOO)tBuY(X)(thf)] (X = CH2TMS, thf = tetrahydrofuran) with tert-butyl-dimethyl-silyl-functionalized α-methylpyridine to obtain the complex [(ONOOtBuY(X)(thf)] (X = 4-(4′-(((tert-butyldimethylsilyl)oxy)methyl)phenyl)-2,6-di-methylpyridine). These initiators served as functional end-groups in polymers produced via REM-GTP. In this contribution, homopolymers of 2-vinylpyridine (2VP) and diethyl vinyl phosphonate (DEVP) were produced. Activity studies and end-group analysis via mass spectrometry, size-exclusion chromatography (SEC) and NMR spectroscopy were performed to reveal the initiator efficiency, the catalyst activity towards both monomers as well as the initiation mechanism of this initiator in contrast to commonly used alkyl initiators. In addition, 2D NMR studies were used to further confirm the end-group integrity of the polymers. For all polymers, different deprotection routes were evaluated to obtain hydroxyl-terminated poly(2-vinylpyridine) (P2VP) and poly(diethyl vinyl phosphonate) (PDEVP). Such hydroxyl groups bear the potential to act as anchoring points for small bioactive molecules, for post-polymerization functionalization or as macroinitiators for further polymerizations. Full article
(This article belongs to the Special Issue Catalysts for C–H Activation and Functionalisation)
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12 pages, 6277 KiB  
Article
YCl3-Catalyzed Highly Selective Ring Opening of Epoxides by Amines at Room Temperature and under Solvent-Free Conditions
by Wuttichai Natongchai, Rais Ahmad Khan, Ali Alsalme and Rafik Rajjak Shaikh
Catalysts 2017, 7(11), 340; https://doi.org/10.3390/catal7110340 - 10 Nov 2017
Cited by 7 | Viewed by 8549
Abstract
A simple, efficient, and environmentally benign approach for the synthesis of β-amino alcohols is herein described. YCl3 efficiently carried out the ring opening of epoxides by amines to produce β-amino alcohols under solvent-free conditions at room temperature. This catalytic approach is very [...] Read more.
A simple, efficient, and environmentally benign approach for the synthesis of β-amino alcohols is herein described. YCl3 efficiently carried out the ring opening of epoxides by amines to produce β-amino alcohols under solvent-free conditions at room temperature. This catalytic approach is very effective, with several aromatic and aliphatic oxiranes and amines. A mere 1 mol % concentration of YCl3 is enough to deliver β-amino alcohols in good to excellent yields with high regioselectivity. Full article
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18 pages, 396 KiB  
Article
Enantioselective Synthesis of 2,2-Disubstituted Terminal Epoxides via Catalytic Asymmetric Corey-Chaykovsky Epoxidation of Ketones
by Toshihiko Sone, Akitake Yamaguchi, Shigeki Matsunaga and Masakatsu Shibasaki
Molecules 2012, 17(2), 1617-1634; https://doi.org/10.3390/molecules17021617 - 7 Feb 2012
Cited by 28 | Viewed by 9550
Abstract
Catalytic asymmetric Corey-Chaykovsky epoxidation of various ketones with dimethyloxosulfonium methylide using a heterobimetallic La-Li3-BINOL complex (LLB) is described. The reaction proceeded smoothly at room temperature in the presence of achiral phosphine oxide additives, and 2,2-disubstituted terminal epoxides were obtained in high [...] Read more.
Catalytic asymmetric Corey-Chaykovsky epoxidation of various ketones with dimethyloxosulfonium methylide using a heterobimetallic La-Li3-BINOL complex (LLB) is described. The reaction proceeded smoothly at room temperature in the presence of achiral phosphine oxide additives, and 2,2-disubstituted terminal epoxides were obtained in high enantioselectivity (97%–91% ee) and yield ( > 99%–88%) from a broad range of methyl ketones with 1–5 mol% catalyst loading. Enantioselectivity was strongly dependent on the steric hindrance, and other ketones, such as ethyl ketones and propyl ketones resulted in slightly lower enantioselectivity (88%–67% ee). Full article
(This article belongs to the Special Issue Asymmetric Catalysis)
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