Catalysts最新文献

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Catalytic Hydrogenation Property of Methyl Benzoate to Benzyl Aldehyde over Manganese-Based Catalysts with Appropriate Oxygen Vacancies 具有适当氧空位的锰基催化剂催化苯甲酸甲酯加氢生成苄醛的性能
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-28 DOI: 10.3390/catal14010027
Pengxiang Gao, Xiaoran Liu, Xindong Mu, Yan Zhang
{"title":"Catalytic Hydrogenation Property of Methyl Benzoate to Benzyl Aldehyde over Manganese-Based Catalysts with Appropriate Oxygen Vacancies","authors":"Pengxiang Gao, Xiaoran Liu, Xindong Mu, Yan Zhang","doi":"10.3390/catal14010027","DOIUrl":"https://doi.org/10.3390/catal14010027","url":null,"abstract":"The synthesis of benzaldehyde, a compound widely utilized in food, medicine, and cosmetics, was achieved through a one-step catalytic hydrogenation using the cost-effective raw material, methyl benzoate. This process aligns with the principles of atom economy and green production. Despite the development of numerous high-performance catalysts by scholars, the challenge remains in achieving lower reaction temperatures, ideally below 400 °C. In this study, a series of MnOx/γ-Al2O3 catalysts were meticulously prepared using the precipitation-impregnation method. These catalysts featured supports calcined at various temperatures and distinct manganese active components. Characterization techniques such as X-ray diffraction (XRD), N2 physical adsorption, Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), H2 temperature programmed reduction (H2-TPR), and NH3 temperature-programmed desorption (NH3-TPD) were employed to analyze the structure and surface properties of the catalysts. Notably, the optimized reaction temperature was found to be 360 °C. The catalyst exhibited the most favorable performance when the calcination temperature of the support was 500 °C and the Mn/Al molar ratio reached 0.18. Under these conditions, the catalyst demonstrated the most suitable oxygen vacancy concentration, yielding impressive results: a conversion rate of 87.90% and a benzaldehyde selectivity of 86.1%. These achievements were attained at 360 °C, atmospheric pressure, a hydrogen to methyl benzoate molar ratio of 40:1, and a Gas Hourly Space Velocity (GHSV) of 800 h−1. This research underscores the potential for optimizing catalysts to enhance the efficiency and sustainability of benzaldehyde synthesis.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"3 11","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139151772","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Steam Treatment Promotion on the Performance of Pt/CeO2 Three-Way Catalysts for Emission Control of Natural Gas-Fueled Vehicles 蒸汽处理对用于天然气燃料汽车排放控制的 Pt/CeO2 三元催化剂性能的促进作用
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-25 DOI: 10.3390/catal14010017
Xi Liu, Yuankai Shao, Xiaoning Ren, Anqi Dong, Kaixiang Li, Bingjie Zhou, Chunqing Yang, Yatao Liu, Zhenguo Li
{"title":"Steam Treatment Promotion on the Performance of Pt/CeO2 Three-Way Catalysts for Emission Control of Natural Gas-Fueled Vehicles","authors":"Xi Liu, Yuankai Shao, Xiaoning Ren, Anqi Dong, Kaixiang Li, Bingjie Zhou, Chunqing Yang, Yatao Liu, Zhenguo Li","doi":"10.3390/catal14010017","DOIUrl":"https://doi.org/10.3390/catal14010017","url":null,"abstract":"Three-way catalyst (TWC) is the mainstream technology for stoichiometric natural gas vehicle gas emission purification to meet the China VI emission standard for heavy-duty vehicles. Due to the high price of Pd-Rh TWC widely used at present, it is of great significance to develop cheaper Pt-only catalysts as substitutes. However, there are few studies on Pt-only TWC, especially for natural gas vehicles. It remains a formidable challenge to develop Pt-only TWC with excellent activity and stability. In this study, we significantly improved the catalytic performance of Pt/CeO2 TWC through thermal treatment, especially steam treatment at 800 °C, and used XRD, TEM, H2-TPR, and XPS techniques to investigate how Pt/CeO2 can be activated via these treatments. Our results suggested that after these treatments, CeO2 crystallites sintered slightly, while platinum particles remained highly dispersed. Moreover, these treatments also weakened the Pt-CeO2 interaction, promoted the formation of oxygen vacancies in CeO2 support, and generated a new type of active surface oxygen in the vicinity of Ptδ+, thus improving the activity of the catalyst. After 800 °C steam treatment, the T50 of CH4 and NO decreased by 31 and 36 °C, respectively. The results obtained in this study provide implications for the synthesis of efficient Pt-based catalysts.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"8 2","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139158112","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Upgrading Epoxy Supports for Enzyme Immobilization by Affinity Function Doping—A Case Study with Phenylalanine Ammonia-Lyase from Petroselinum crispum 通过亲和功能掺杂提升酶固定化环氧支撑物的性能--以来自脆皮草的苯丙氨酸氨化-裂解酶为例进行研究
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-23 DOI: 10.3390/catal14010014
Bálint Alács, Anna Zrinyi, Gábor Hornyánszky, László Poppe, Evelin Bell
{"title":"Upgrading Epoxy Supports for Enzyme Immobilization by Affinity Function Doping—A Case Study with Phenylalanine Ammonia-Lyase from Petroselinum crispum","authors":"Bálint Alács, Anna Zrinyi, Gábor Hornyánszky, László Poppe, Evelin Bell","doi":"10.3390/catal14010014","DOIUrl":"https://doi.org/10.3390/catal14010014","url":null,"abstract":"This article provides a method to upgrade epoxy-functionalized carriers for covalent enzyme immobilization to selective carriers suitable for covalent immobilization of metal affinity-tagged enzymes without the need of preliminary enzyme purification. Affinity function doping of the epoxy-functionalized surface introduces an advanced possibility to avoid the costly and time-consuming downstream processes required for efficient immobilization on non-selective epoxy carriers. Our approach is based on the partial functionalization of surface epoxides via a proper diamine-derived linker and an ethylenediaminetetraacetic dianhydride-based chelator charged with cobalt ions. The solid macroporous carriers, doped with metal affinity functions, have both coordinative binding ability (rapid anchoring the metal affinity-tagged enzymes to the surface) and subsequent covalent bond-forming ability (preferred binding of the tagged enzyme to the surface after proper washing by the residual epoxide functions), enabling a single operation for the enrichment and immobilization of a recombinant phenylalanine ammonia-lyase from parsley fused to a polyhistidine affinity tag. The immobilized PcPAL was applied in the ammonia elimination of racemic phenylalanine, 4-chlorophenylalanine, and 4-bromophenylalanine to produce the corresponding d-phenylalanines, in addition to the formation of (E)-cinnamates, as well as in ammonia addition reactions to (E)-cinnamates, yielding the corresponding enantiopure l-phenylalanines.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"257 1","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139163211","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Measurements of Dioxygen Formation in Catalytic Electrochemical Water Splitting 测量催化电化学水分离过程中的二氧生成量
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-22 DOI: 10.3390/catal14010013
C. Tiwari, Y. Geletii
{"title":"Measurements of Dioxygen Formation in Catalytic Electrochemical Water Splitting","authors":"C. Tiwari, Y. Geletii","doi":"10.3390/catal14010013","DOIUrl":"https://doi.org/10.3390/catal14010013","url":null,"abstract":"Water oxidation is a multielectron complex reaction that produces molecular oxygen as the final product. The article addresses the lack of confirmation of oxygen product formation in electrochemical oxygen evolution reaction (OER) studies, despite the extensive research conducted on catalysts for water splitting. It critically evaluates the trend observed in many studies that solely rely on electrochemical methods for OER quantification without confirming the oxygen product via complementary analytical techniques. The omission of measuring evolved oxygen gas leaves a crucial gap in the quantification of the OER process and raises concerns about the validity and accuracy of reported results. Analytical techniques, such as gas chromatography, Rotating Ring-Disk Electrode (RRDE), fluorescence oxygen probes, Clark electrode, and volumetry are critically analyzed and described to ensure the reliability and credibility of voltammetry and bulk electrolysis to provide a more accurate assessment of the OER process.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"3 12","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138944215","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ca2Fe2O5-Based WGS Catalysts to Enhance the H2 Yield of Producer Gases 基于 Ca2Fe2O5 的 WGS 催化剂提高生产气体的 H2 产率
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-21 DOI: 10.3390/catal14010012
I. Antunes, L. Ruivo, L. Tarelho, Jorge R. Frade
{"title":"Ca2Fe2O5-Based WGS Catalysts to Enhance the H2 Yield of Producer Gases","authors":"I. Antunes, L. Ruivo, L. Tarelho, Jorge R. Frade","doi":"10.3390/catal14010012","DOIUrl":"https://doi.org/10.3390/catal14010012","url":null,"abstract":"Ca2Fe2O5-based catalysts were synthesized from siderite and calcite precursors, which were processed in the form of pelletized samples and tested as water gas shift catalysts. Catalytic tests were performed in a tubular reactor, at temperatures in the range 400–500 °C and with different H2O:CO ratios, diluted with N2; this demonstrates the positive impact of Ca2Fe2O5 on conversion of CO and H2 yield, relative to corresponding tests without catalyst. The catalytic performance was also remarkably boosted in a microwave-heated reactor, relative to conventional electric heating. Post-mortem analysis of spent catalysts showed significant XRD reflections of spinel phases (Fe3O4 and CaFe2O4), and SiO2 from the siderite precursor. Traces of calcium carbonate were also identified, and FTIR analysis revealed relevant bands ascribed to calcium carbonate and adsorbed CO2. Thermodynamic modelling was performed to assess the redox tolerance of Ca2Fe2O5-based catalysts in conditions expected for gasification of biomass and thermochemical conditions at somewhat lower temperatures (≤500 °C), as a guideline for suitable conditions for water gas shift. This modelling, combined with the results of catalytic tests and post-mortem analysis of spent catalysts, indicated that the O2 and CO2 storage ability of Ca2Fe2O5 contributes to its catalytic activity, suggesting prospects to enhance the H2 content of producer gases by water gas shift.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"38 20","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138948789","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced Low-Temperature Activity and Hydrothermal Stability of Ce-Mn Oxide-Modified Cu-SSZ-39 Catalysts for NH3-SCR of NOx 增强用于氮氧化物 NH3-SCR 的 Ce-Mn Oxide 改性 Cu-SSZ-39 催化剂的低温活性和水热稳定性
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-21 DOI: 10.3390/catal14010010
Ahui Tang, Fuzhen Yang, Ying Xin, Xiaoli Zhu, Long Yu, Shuai Liu, Dongxu Han, Junxiu Jia, Yaning Lu, Zhenguo Li, Zhaoliang Zhang
{"title":"Enhanced Low-Temperature Activity and Hydrothermal Stability of Ce-Mn Oxide-Modified Cu-SSZ-39 Catalysts for NH3-SCR of NOx","authors":"Ahui Tang, Fuzhen Yang, Ying Xin, Xiaoli Zhu, Long Yu, Shuai Liu, Dongxu Han, Junxiu Jia, Yaning Lu, Zhenguo Li, Zhaoliang Zhang","doi":"10.3390/catal14010010","DOIUrl":"https://doi.org/10.3390/catal14010010","url":null,"abstract":"Cu-SSZ-39 zeolite with an AEI structure exhibits excellent hydrothermal stability and can be a potential alternative to Cu-SSZ-13 zeolite SCR catalysts for NOx removal in diesel vehicles. However, the inferior low-temperature performance of Cu-SSZ-39 leads to substantial NOx emissions during the cold-start period, impeding its practical application. In this study, Ce-Mn oxide-modified Cu-SSZ-39 catalysts (CeMnOx/Cu-SSZ-39) and references (CeO2/Cu-SSZ-39 and MnOx/Cu-SSZ-39) were prepared by the ion-exchange of Cu ions followed by impregnation of the oxide precursors, with the aim of enhancing the NH3-SCR performance at low temperatures. The modified catalysts exhibited improved low-temperature activity and hydrothermal stability compared to the unmodified counterpart. In particular, CeMnOx/Cu-SSZ-39 showed the highest activity among the three catalysts and achieved NOx conversions above 90% within the temperature range of 180 °C to 600 °C, even after undergoing hydrothermal aging at 800 °C. Experimental results indicated that the synergistic effect between Ce and Mn in CeMnOx improves the redox properties and acidity of the catalyst due to the presence of Ce3+, Mn4+, and abundant adsorbed oxygen species, which facilitate low-temperature SCR reactions. Furthermore, the interaction of CeMnOx with Cu-SSZ-39 stabilizes the zeolite framework and hinders the agglomeration of Cu species during the hydrothermal aging process, contributing to its exceptional hydrothermal stability. The kinetics and NO oxidation experiments demonstrated that CeMnOx provides access to fast SCR reaction pathways by oxidizing NO to NO2, resulting in a significant increase in low-temperature activity. This study provides novel guidelines for the design and preparation of Cu-SSZ-39 zeolite with outstanding SCR performance over a wide temperature range.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"38 25","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138950154","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dimension Engineering in Noble-Metal-Based Nanocatalysts 贵金属基纳米催化剂的尺寸工程学
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-20 DOI: 10.3390/catal14010009
Bei Liu, Haosen Yang, Pengfei Hu, Guangsheng Wang, Yongqiang Guo, Hewei Zhao
{"title":"Dimension Engineering in Noble-Metal-Based Nanocatalysts","authors":"Bei Liu, Haosen Yang, Pengfei Hu, Guangsheng Wang, Yongqiang Guo, Hewei Zhao","doi":"10.3390/catal14010009","DOIUrl":"https://doi.org/10.3390/catal14010009","url":null,"abstract":"Catalysts play a pivotal role in modern industries, such as energy, pharmaceuticals, and petrochemicals, serving as cornerstone of high-tech production. Noble metals, such as gold, silver, and platinum group elements, possess the superb catalytic characteristics of high-temperature oxidation resistance, corrosion resistance, stable electrochemical performance, high catalytic activity, and so on. These characteristics offer excellent prospects for applications in catalysis. In this review, we summarize innovative approaches to regulating the size and morphology of nano-noble metal catalysts with different dimensions. We also showcase typical prominent examples of their applications in exhaust gas purification, battery manufacturing, water splitting, and selective hydrogenation. Finally, perspectives are discussed in terms of future research opportunities in the realm of noble metal nanocatalysts.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"17 14","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139168972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Optimizing Graphene Dopants for Direct Electrocatalytic Quantification of Small Molecules and Ions 优化石墨烯掺杂剂,实现小分子和离子的直接电催化定量
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-20 DOI: 10.3390/catal14010008
Qingwei Zhou, Mingjiao Shi, Mengfan Wu, Ningbin Zhao, Peizheng Shi, Yangguang Zhu, Aiwu Wang, Chen Ye, Cheng-Te Lin, Li Fu
{"title":"Optimizing Graphene Dopants for Direct Electrocatalytic Quantification of Small Molecules and Ions","authors":"Qingwei Zhou, Mingjiao Shi, Mengfan Wu, Ningbin Zhao, Peizheng Shi, Yangguang Zhu, Aiwu Wang, Chen Ye, Cheng-Te Lin, Li Fu","doi":"10.3390/catal14010008","DOIUrl":"https://doi.org/10.3390/catal14010008","url":null,"abstract":"This review critically evaluates the recent advancements in graphene dopants for electrocatalytic quantification of small molecules and ions. Emphasizing the enhanced catalytic activity and specificity of doped graphene, the paper delves into the various doping methods, ranging from chemical to physical techniques. It presents a detailed analysis of the mechanisms underlying graphene-based electrocatalysis and its applications in environmental monitoring, health care, and pharmaceuticals. The review also addresses challenges such as the reproducibility and stability of doped graphene, suggesting future research directions. By summarizing the latest findings, this review aims to elucidate the role of doped graphene in improving the sensitivity and selectivity of electrocatalytic processes, bridging the gap between research and practical use.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"120 44","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138953970","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nitrogen-Rich Tetrazole–Amide-Functionalised Zn Metal–Organic Framework as Catalyst for Efficient Catalytic CO2 Cycloaddition with Epoxides 富氮四唑-酰胺官能化 Zn 金属有机框架作为催化剂高效催化 CO2 与环氧化物的环加成反应
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-20 DOI: 10.3390/catal14010006
Anup Paul, Ismayil M. Garazade, Anirban Karmakar, R. A. Khan, M. F. C. Guedes da Silva, Ana V M Nunes, A. Pombeiro
{"title":"Nitrogen-Rich Tetrazole–Amide-Functionalised Zn Metal–Organic Framework as Catalyst for Efficient Catalytic CO2 Cycloaddition with Epoxides","authors":"Anup Paul, Ismayil M. Garazade, Anirban Karmakar, R. A. Khan, M. F. C. Guedes da Silva, Ana V M Nunes, A. Pombeiro","doi":"10.3390/catal14010006","DOIUrl":"https://doi.org/10.3390/catal14010006","url":null,"abstract":"In this study, we report the design, synthesis, and catalytic application of the novel nitrogen-rich Zn(II) MOF [Zn2(μ3-1κN,2κN′,3κO-HL)2(DMF)2]n·nH2O (HL2− = 4-((4-(1H-tetrazol-5-yl)phenyl)carbamoyl)benzoate), denoted as ZnMOF, for the efficient conversion of carbon dioxide (CO2) to cyclic carbonates via cycloaddition with epoxides. It was synthesised from a tetrazole appended amide-functionalised pro-ligand (H3L) and Zn(NO3)2·6H2O under hydrothermal conditions. The synthesised material was characterised namely by elemental analysis, infrared spectroscopy, powder X-ray diffraction (PXRD), and single-crystal X-ray diffraction analyses. The catalytic potential of ZnMOF was investigated in the CO2 cycloaddition reaction with various epoxides, with conversions ranging from 17% to 99%. The catalyst retained its activity across multiple reaction cycles, demonstrating its stability and reusability. The influence of co-catalysts on the reaction was explored, with tetrabutylammonium bromide (TBABr) emerging as the most effective one. A plausible reaction mechanism is proposed.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"91 11","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138954379","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Highly Efficient and Magnetically Recyclable Non-Noble Metal Fly Ash-Based Catalysts for 4-Nitrophenol Reduction 基于磁性可回收非贵金属粉煤灰的高效 4-硝基苯酚还原催化剂
IF 3.9 3区 化学
Catalysts Pub Date : 2023-12-19 DOI: 10.3390/catal14010003
I. Kuźniarska-Biernacka, Inês Ferreira, Marta Monteiro, A. C. Santos, Bruno Valentim, Alexandra Guedes, João H. Belo, João P. Araújo, Cristina Freire, A. F. Peixoto
{"title":"Highly Efficient and Magnetically Recyclable Non-Noble Metal Fly Ash-Based Catalysts for 4-Nitrophenol Reduction","authors":"I. Kuźniarska-Biernacka, Inês Ferreira, Marta Monteiro, A. C. Santos, Bruno Valentim, Alexandra Guedes, João H. Belo, João P. Araújo, Cristina Freire, A. F. Peixoto","doi":"10.3390/catal14010003","DOIUrl":"https://doi.org/10.3390/catal14010003","url":null,"abstract":"4-nitrophenol (4-NPh) is a harmful compound produced in large amounts in the chemical industry, and its reduction to aminophenol (4-APh) using noble metals as catalysts is one of the most studied processes. The development of noble metal-free catalysts represents an economic advantage in large-scale applications and contributes to the sustainability of raw materials. Coal fly ash (FA), a major waste stream from coal combustion, contains an easily recoverable magnetic fraction (FAmag sample) composed of Fe-rich particles that could substitute noble metal catalysts in 4-NPh reduction, with the concomitant advantage of being easily recovered via magnetic separation. For this purpose, a new composite material containing copper ferrite nanoparticles (FAmag@CS@CuFe) was prepared via a facile, environmentally friendly and cost-effective method based on three components: FAmag as the core, a biobased polymer chitosan (CS) as the linker and copper ferrite CuFe2O4 nanoparticles (CuFe) as the active sites. The structure, morphology, composition and magnetic properties of the FAmag@CS@CuFe material were studied to assess the efficiency of the preparation. It was found that the biopolymer prevented the aggregation of CuFe nanoparticles and enabled a synergistically outstanding activity towards the reduction of 4-NPh in comparison to the pristine FAmag and bare CuFe nanoparticles. The FAmag@CS@CuFe catalyst showed efficiency and stability in the conversion of 4-NPh of up to 95% in 3 min over four consecutive cycles. Such remarkable catalytic results demonstrate the potential of this catalyst as a substitute for expensive noble metals.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":" 76","pages":""},"PeriodicalIF":3.9,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138962225","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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