4.7 Article

Approaches to the synthesis of Pd/C catalysts with controllable activity and selectivity in hydrogenation reactions

期刊

CATALYSIS TODAY
卷 357, 期 -, 页码 152-165

出版社

ELSEVIER
DOI: 10.1016/j.cattod.2019.03.023

关键词

Palladium catalysts; Carbon support; Catalytic hydrogenation; Controllable activity; Controllable selectivity

资金

  1. Ministry of Science and Higher Education of the Russian Federation
  2. Fundamental Research Program of State Academies of Sciences [V.47.1.3, AAAA-A17-117021450099-9]

向作者/读者索取更多资源

Carbon-supported palladium catalysts are widely used for hydrogenation of various organic compounds in the fine chemical industry. The nanoscale geometry and electronic structure of supported Pd nanoparticles play a crucial role in providing the necessary catalytic properties. To improve catalytic activity and selectivity of Pd nanoparticles, it is possible to fine tune their intrinsic properties (e.g., size and oxidation state) by controlling the chemical transformations at different stages of catalyst preparation. Recent years have seen considerable advancement in developing new catalyst preparation techniques as well as in understanding the mechanism of active site formation. This review summarizes some of the existing approaches to regulating the catalytic properties of carbon-supported palladium by variation of the carbon support, the composition of palladium precursor and its reduction conditions, as well as the addition of a second active metal. The data presented may be useful for researchers developing efficient Pd/C catalysts for hydrogenation of polyfunctional organic compounds.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Chemistry, Multidisciplinary

Solvent effect on the rate and direction of furfural transformations during hydrogenation over the Pd/C catalyst

R. M. Mironenko, O. B. Belskaya, V. A. Likholobov

Summary: The rate and selectivity of the liquid-phase hydrogenation of furfural depend on the chemical nature of the catalyst and solvent.

RUSSIAN CHEMICAL BULLETIN (2022)

Review Chemistry, Multidisciplinary

Nanoglobular carbon and palladium-nanoglobular carbon catalysts for liquid-phase hydrogenation of organic compounds

Roman M. Mironenko, Vladimir A. Likholobov, Olga B. Belskaya

Summary: The results of studies related to the development of palladium +/- carbon catalyst and the mechanisms involved are analyzed and integrated in this paper. The focus is on Pd/NGC compositions (NGC is nanoglobular carbon), and the methods for preparing NGC, particularly carbon black, are considered. The paper also discusses the factors influencing the catalytic properties of Pd/NGC and compares it with other carbon-supported palladium catalysts. The bibliography includes 623 references.

RUSSIAN CHEMICAL REVIEWS (2022)

Article Chemistry, Physical

Metal-catalyzed chemical activation of calcium carbide: New way to hierarchical metal/alloy-on-carbon catalysts

Andrey N. Lebedev, Konstantin S. Rodygin, Roman M. Mironenko, Elina R. Saybulina, Valentine P. Ananikov

Summary: A simple and efficient strategy for synthesizing metal/alloy-on-carbon catalysts has been developed, resulting in highly active catalysts with intrinsic hierarchical organization, excellent stability, and high selectivity.

JOURNAL OF CATALYSIS (2022)

Article Chemistry, Physical

Catalysts Derived from Nickel-Containing Layered Double Hydroxides for Aqueous-Phase Furfural Hydrogenation

Olga B. Belskaya, Roman M. Mironenko, Tatiana Gulyaeva, Mikhail Trenikhin, Ivan Muromtsev, Svetlana Trubina, Valentina V. Zvereva, Vladimir A. Likholobov

Summary: The changes in the properties and state of nickel in the synthesis of nickel catalysts using NiAl-layered double hydroxides were investigated. It was found that the use of NiAl LDH as the catalyst precursor allows for the obtaining of active dispersed nickel particles, and higher catalyst reduction temperature leads to increased catalyst activity and conversion rate.

CATALYSTS (2022)

Article Chemistry, Physical

Porous Carbon-Carbon Composite Materials Obtained by Alkaline Dehydrochlorination of Polyvinyl Chloride

Yury G. Kryazhev, Irina V. Anikeeva, Mikhail V. Trenikhin, Tatiana I. Gulyaeva, Valeriy P. Melnikov, Vladimir A. Likholobov, Olga B. Belskaya

Summary: Porous carbon-carbon composite materials were synthesized using polyvinyl chloride solutions in dimethyl sulfoxide and modifying additives. The obtained composites showed a porous carbon structure with either carbon nanoglobules or crumpled sheet carbon particles, depending on the additives used. The study analyzed transmission electron microscopy images to study local areas of the materials and determine the distances between graphene layers. The synthesized materials showed varying fractions of mesopores and specific surface areas, making them suitable for various applications.

MATERIALS (2022)

Article Energy & Fuels

Nickel catalysts based on carbon-mineral supports derived from sapropel for hydroliquefaction of sapropel organic matter

E. N. Terekhova, O. B. Belskaya, M. V. Trenikhin, A. V. Babenko, I. V. Muromtzev, V. A. Likholobov

Summary: Carbon-mineral supports obtained from carbonization of sapropels were used to synthesize nickel-containing catalysts. The study investigated the effect of catalyst composition on the catalytic hydroliquefaction of sapropel organic matter. Catalysts based on a support prepared from mineral-type sapropel showed higher activity.
Article Chemistry, Physical

Nickel Catalysts on Carbon-Mineral Sapropel-Based Supports for Liquid-Phase Hydrogenation of Nitrobenzene

Elena N. Terekhova, Olga B. Belskaya, Rinat R. Izmaylov, Mikhail V. Trenikhin, Vladimir A. Likholobov

Summary: Nickel catalysts were synthesized using carbon-mineral supports derived from sapropel, and the effect of support nature and active component precursor on catalytic activity in liquid-phase nitrobenzene hydrogenation was studied. Catalysts with a smaller fraction of carbon in the support exhibited higher activity regardless of the precursor nature. The catalysts synthesized using nickel nitrate and nickel formate showed the highest activity with nitrobenzene conversion of 65% and 51% respectively after 1 hour of reaction. The catalysts maintained high activity with 100% aniline selectivity after six reaction cycles. The presence of sulfur in the nickel precursor decreased catalytic activity (conversion less than 3%) due to the formation of the sulfide phase.

CATALYSTS (2023)

Article Chemistry, Inorganic & Nuclear

Synthesis of CuAl-LDHs by Co-Precipitation and Mechanochemical Methods and Selective Hydrogenation Catalysts Based on Them

Olga B. Belskaya, Elena N. Terekhova, Oksana V. Gorbunova, Ivan V. Muromtsev, Mikhail V. Trenikhin, Aleksei N. Salanov, Vladimir A. Likholobov

Summary: The paper discusses the synthesis and application of CuAl layered double hydroxides (LDHs) as catalysts for selective hydrogenation. Homogeneous LDHs were obtained through co-precipitation and mechanochemical methods, and the important parameters for their formation were identified. The co-precipitation method was found to be most influenced by pH and CO32-/Al3+ ratio, while mechanochemical synthesis allowed for shorter synthesis time and improved catalytic activity. Both catalysts showed high selectivity for double bond hydrogenation with significantly higher conversion for the mechanochemically synthesized sample.

INORGANICS (2023)

Review Chemistry, Physical

Aqueous-Phase Hydrogenation of Furfural in the Presence of Supported Metal Catalysts of Different Types. A Review

R. M. Mironenko, O. B. Belskaya, V. A. Likholobov

Summary: Hydrogenation of furfural with heterogeneous catalysts is a promising method for synthesizing oxygen-containing compounds from renewable raw materials. The composition of the catalyst and its preparation conditions determine the predominant routes of reductive conversions during furfural hydrogenation. This review discusses methods for controlling the physicochemical and functional properties of Pd, Ni, Co, and Cu-containing catalytic compositions and their influence on the activity and selectivity of supported catalysts in furfural hydrogenation under aqueous-phase conditions.

DOKLADY PHYSICAL CHEMISTRY (2023)

Review Chemistry, Multidisciplinary

Intermolecular hydrogen transfer reactions as key stages in the catalytic cracking: achievements and outlook

Oleg Potapenko, Vladimir P. Doronin, Tatyana P. Sorokina, Vladimir A. Likholobov

Summary: The review summarizes and critically analyzes recent exploratory and basic studies on hydrogen transfer reactions in hydrocarbon conversion processes. It discusses the regularities of these reactions in various systems, focusing on the role of intermolecular hydrogen transfer in zeolite-catalyzed cracking of hydrocarbons. The review also includes data on the development and properties of zeolite-based catalysts for hydrocarbon cracking.

RUSSIAN CHEMICAL REVIEWS (2023)

Article Chemistry, Applied

Operando characterisation of the products of Fischer-Tropsch synthesis in a fixed-bed reactor studied by magnetic resonance

Qingyuan Zheng, Jack H. Williams, Scott Elgersma, Mick D. Mantle, Andrew J. Sederman, G. Leendert Bezemer, Constant M. Guedon, Lynn F. Gladden

Summary: In this study, a pilot-scale fixed-bed reactor compatible with NMR/MRI was developed for Fischer-Tropsch synthesis. Multiple magnetic resonance techniques were applied to quantitatively characterize different product species within catalyst pellets, providing valuable information for catalyst and reactor optimization.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Ambient pressure operando catalytic characterization by combining PM-IRRAS with planar laser-induced fluorescence and surface optical reflectance imaging

Lisa Ramisch, Sebastian Pfaff, Sabrina M. Gericke, Edvin Lundgren, Johan Zetterberg

Summary: We present a combination of optical operando techniques that allow simultaneous measurement of adsorbed species on catalyst surfaces, monitoring of surface oxide formation, and imaging of the gas phase above the catalyst surface. The experimental setup was validated by studying CO oxidation on Pd(100) at different pressures, revealing the effects of pressure on the heterogeneous catalytic reaction.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Insights into the influence of feed impurities on catalytic performance in the solvent-free dimerization of renewable levulinic acid

Marta Paniagua, Gabriel Morales, Juan A. Melero, Daniel Garcia-Salgado

Summary: The influence of common impurities in levulinic acid on the catalytic performance of different acid catalysts for bio-jet fuel production was studied. It was found that furfural had the greatest detrimental effect on catalyst performance, while propyl-sulfonic acid-modified SBA-15 and sulfonic acid resin Amberlyst-70 showed good regeneration ability.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Open Zn-URJC-13 efficient catalyst for mild CO2 transformation using bulky epoxides

Jesus Tapiador, Pedro Leo, Guillermo Calleja, Gisela Orcajo

Summary: This study presents a new MOF material, Zn-URJC-13, with acid and basic sites, permanent porosity, and high affinity to CO2 molecules. The Zn-URJC-13 catalyst exhibits efficient performance in CO2 cycloaddition reactions and can be reused multiple times.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Effect of supports on the kind of in-situ formed ZnOx species and its consequence for non-oxidative propane dehydrogenation

Dan Zhao, Vita A. Kondratenko, Dmitry E. Doronkin, Shanlei Han, Jan-Dierk Grunwaldt, Uwe Rodemerck, David Linke, Evgenii V. Kondratenko

Summary: This study demonstrates the potential of cheap and commercially available Zr or Ti-based supports and ZnO to serve as active and selective catalysts for propane dehydrogenation (PDH). The catalytically active species formed in situ under PDH conditions consist of isolated ZnOx. ZnOx on the surface of LaZrOx shows the highest rate of propene formation.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Diels-Alder conversion of biomass-derived furans and ethylene to renewable aromatics over mesoporous titanium phosphate

Hanbyeol Kim, Jung Rae Kim, Young-Kwon Park, Jeong-Myeong Ha, Jungho Jae

Summary: In this study, metal phosphates were used as catalysts for biomass conversion to produce sustainable aromatics through DielsAlder cycloaddition reactions. The effects of synthesis method, activation method, and P/Ti molar ratio on the structure and acid properties of titanium phosphate catalysts were systematically studied. The mesoporous titanium phosphate catalyst synthesized by hydrothermal method at 180℃ for 12 h followed by ethanol refluxing at 60℃ for 24 h at a molar P/Ti ratio of 1 showed the highest surface area and acid site density.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

High propylene selectivity in methanol conversion over metal (Sm, Y, and Gd) modified HZSM-5 catalysts in the methanol to propylene process

Yasin Khani, Sumin Pyo, Kwang-Eun Jeong, Chul-Ung Kim, Moonis Ali Khan, Byong-Hun Jeon, Kun-Yi Andrew Lin, Siyoung Q. Choi, Young-Kwon Park

Summary: A protonated form of Zeolite Socony Mobil-5 (H-ZSM-5) catalyst was synthesized through a hydrothermal method using different sources of silica. The effect of loading the catalyst with yttrium, samarium, and gadolinium on the acidic properties was investigated. Among the metal-loaded catalysts, the Sm/LHZ catalyst showed the best performance in the methanol to propylene conversion due to its high amount of weak and intermediate acid sites, while the Gd-LHZ catalyst increased the selectivity towards ethane and propane.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Enantioselective synthesis of spiroimidazolones by synergistic catalysis

Michael Franc, Ivana Cisarova, Jan Vesely

Summary: The present study investigates an enantioselective cyclization of enals with imidazolone derivatives catalyzed by a combination of achiral Pd(0) complex and chiral secondary amine. Corresponding spirocyclic imidazolones were produced in high yields with moderate diastereoselectivity and excellent enantioselectivity. The developed co-operative catalytic methodology provides a highly substituted spirocyclic scaffold with four stereogenic centers under mild conditions.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Influence of the synthesis method of Cu/Y zeolite catalysts for the gas phase oxidative carbonylation of methanol to dimethyl carbonate

Mauro Alvarez, Jennifer Cueto, David P. Serrano, Pablo Marin, Salvador Ordonez

Summary: This study focuses on improving the formulation and preparation methods of catalysts for the production of dimethyl carbonate. By using suitable catalyst preparation methods and copper salt precursors, the researchers successfully produced catalysts with optimal performance for dimethyl carbonate formation.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Influence of Ag particle size and Ag : Al2O3 surface ratio in catalysts for the chloride-promoted ethylene epoxidation

Claudia J. Keijzer, Luc C. J. Smulders, Dennie Wezendonk, Jan Willem de Rijk, Petra E. de Jongh

Summary: This study investigates the catalytic behavior of alpha-alumina supported silver catalysts in the presence of chloride. It is found that the particle size of silver can affect the selectivity of the catalyst, but different strategies lead to different results. In this size range, the selectivity of ethylene oxide is correlated to the Ag : Al2O3 surface ratio.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Acid and base catalysis of SrTiO3 nanoparticles for C-C bond-forming reactions

Takeshi Aihara, Wataru Aoki, Michikazu Hara, Keigo Kamata

Summary: The development of acid-base bifunctional catalysts is important for promoting specific chemical transformations. In this study, Ti-based perovskite oxides were synthesized and used as catalysts for two C-C bond-forming reactions (cyanosilylation and Knoevenagel condensation). The highly pure SrTiO3 nanoparticles with a high specific surface area exhibited the highest catalytic performance, and could be easily recovered and reused.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

New Sn-Mg-Al hydrotalcite-based catalysts for Baeyer-Villiger oxidation of β-cyclocitral

Olga Gorlova, Petra Pribylova, Eliska Vyskocilova, Katerina Peroutkova, Jan Kohout, Iva Paterova

Summary: This study investigates the Baeyer-Villiger oxidation of beta-cyclocitral using tin-modified mixed oxides as catalysts. The optimal reaction conditions and the effects of various factors on the reaction course and selectivity were determined. The results show that tin-modified mixed oxides exhibit high activity and selectivity in the oxidation reaction.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Catalytic upgrading of lignin-derived bio-oils over ion-exchanged H-ZSM-5 and H-beta zeolites

M. I. Avila, M. M. Alonso-Doncel, L. Briones, G. Gomez-Pozuelo, J. M. Escola, D. P. Serrano, A. Peral, J. A. Botas

Summary: The catalytic fast pyrolysis of lignin using ion-exchanged zeolite catalysts showed significant improvements in bio-oil quality and the production of aromatic hydrocarbons and oxygenated compounds.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Simultaneous catalytic dehydration of methanol and ethanol: How ZSM-5 acidity addresses conversion and products distribution

Enrico Catizzone, Giorgia Ferrarelli, Paolo Bruno, Girolamo Giordano, Massimo Migliori

Summary: The acid-catalysed alcohol conversion reaction is a promising route for de-fossilization strategies. Research on pure alcohol conversion and simultaneous dehydration of mixed alcohols have shown different product compositions, with the type and distribution of acid sites affecting the reaction mechanism.

CATALYSIS TODAY (2024)

Article Chemistry, Applied

Effect of oxygen vacancy modification of ZnO on photocatalytic degradation of methyl orange: A kinetic study

Alireza Ranjbari, Juho Kim, Jihee Yu, Jiyun Kim, Mireu Park, Nayoung Kim, Kristof Demeestere, Philippe M. Heynderickx

Summary: This study investigated a novel kinetic model for the adsorption and photocatalytic degradation of methyl orange using commercial ZnO and reduced ZnO photocatalysts. The results provided new insights into the interaction of catalysts with molecules of different charges and compared with a previous study on methylene blue. The presence of oxygen vacancies in ZnO and their effects on adsorption and photocatalytic degradation were analyzed, and the photocatalytic degradation rate of reduced ZnO was found to increase significantly.

CATALYSIS TODAY (2024)