Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Radical Reactivity: Steric Effects01:10

Radical Reactivity: Steric Effects

1.9K
The presence of electron-donating, electron-withdrawing, or conjugating groups adjacent to a radical center, imparts electronic stabilization to the radicals. Examples of such electronically-stabilized radicals are triphenylmethyl, tetramethylpiperidine‐N‐oxide, and 2,2‐diphenyl‐1‐picrylhydrazyl. These radicals are remarkably stable and are known as persistent radicals. Some of the persistent radicals can even be isolated and purified.
Along with electronic...
1.9K
Properties of Transition Metals02:58

Properties of Transition Metals

26.2K
Transition metals are defined as those elements that have partially filled d orbitals. As shown in Figure 1, the d-block elements in groups 3–12 are transition elements. The f-block elements, also called inner transition metals (the lanthanides and actinides), also meet this criterion because the d orbital is partially occupied before the f orbitals.
26.2K
Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

12.2K
Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
12.2K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Operando Tracking of Atomic Hydrogen Dynamics and Lifetime Extension for Nitrate-to-Ammonia Electroreduction.

Environmental science & technology·2026
Same author

Stable Single-Pass Electrochemical Oxidation of Trace 1,4-Dioxane in Groundwater via Multistage Reactors with Current Pulsing.

ACS ES&T engineering·2026
Same author

Reconstruction and Dissolution of Copper Catalysts during Electrocatalytic Nitrate Reduction.

Environmental science & technology·2026
Same author

Three-Dimensional DNA Nanostructure-Assisted Multiplexed Aptamer Assay for Simultaneous Detection of Endocrine-Disrupting Chemical Clusters.

ACS sensors·2026
Same author

Reaction Mechanism of Electrodeposited ε-MnO<sub>2</sub>: A Proton-Centered Pathway in Aqueous Zn-Ion Systems.

ACS applied materials & interfaces·2026
Same author

Ceramic Glazing to Enhance Stability and Selectivity of CoAl<sub>2</sub>O<sub>4</sub> Catalyst for Wastewater Advanced Oxidation.

Environmental science & technology·2026

相关实验视频

Updated: Jul 17, 2025

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
11:44

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions

Published on: March 20, 2014

25.5K

在水性还原条件下,单原子 (不) 稳定性.

Kali Rigby1,2, Dahong Huang1, Denis Leshchev3

  • 1Department of Chemical and Environmental Engineering, Yale University, New Haven, Connecticut 06520, United States.

Environmental science & technology
|August 31, 2023
PubMed
概括

在二氧化上的单原子可以增强4 - 二醇脱. 过渡到集群可以提高反应速度,同时保持选择性,强调催化剂稳定性的重要性.

关键词:
集群集群是一个集群集群.液化脱的方法是:在现场 XASAS XAS.一个原子催化剂稳定的稳定性 稳定的稳定性

更多相关视频

Ligand-Mediated Nucleation and Growth of Palladium Metal Nanoparticles
11:54

Ligand-Mediated Nucleation and Growth of Palladium Metal Nanoparticles

Published on: June 25, 2018

10.4K
Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
19:58

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions

Published on: July 30, 2017

9.7K

相关实验视频

Last Updated: Jul 17, 2025

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
11:44

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions

Published on: March 20, 2014

25.5K
Ligand-Mediated Nucleation and Growth of Palladium Metal Nanoparticles
11:54

Ligand-Mediated Nucleation and Growth of Palladium Metal Nanoparticles

Published on: June 25, 2018

10.4K
Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
19:58

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions

Published on: July 30, 2017

9.7K

科学领域:

  • 催化剂是一种催化剂.
  • 材料科学 材料科学 材料科学
  • 环境化学环境化学

背景情况:

  • 单原子催化剂 (SAC) 提供高效率,但存在不稳定性.
  • 对二氧化 (TiO2) 上的 (Pd) 单个原子进行环境修复的探索.
  • 了解Pd SAC稳定性对于实际应用至关重要.

研究的目的:

  • 为了研究单原子Pd在TiO2上的稳定性和性能,用于4-二醇脱.
  • 在还原性水性条件下确定影响Pd单原子稳定性的因素.
  • 为了将催化剂转换与脱活性和选择性相关联.

主要方法:

  • 在TiO2.2上合成单原子Pd.
  • 对4-二脱的催化性能进行评估.
  • 在现场和现场的X射线吸收光谱 (XAS) 用于动态结构分析.
  • 评估诸如原子分散,协调和基质特性等因素.

主要成果:

  • 单原子 Pd 在 TiO2 上在还原性水性条件下表现出稳定性.
  • 从单个原子过渡到无形集群显著提高了脱化动力学.
  • 催化剂转换没有影响碳键的选择性.
  • 无形星团具有独特的不和协调和几纳米直径.

结论:

  • 催化剂稳定性与脱反应中的性能密切相关.
  • 单个原子的动态转化为集群可以增强催化活性.
  • 详细的表征对于识别反应的真正活性物种至关重要.
  • 优化的Pd/TiO2系统显示出对高效和选择性环境修复的承诺.