通过单原子催化剂在水处理中产生反应性物种
Virender K Sharma1, Xingmao Ma2, Radek Zboril3,4
1Program for the Environment and Sustainability, Department of Environmental and Occupational Health, Texas A&M University, College Station, Texas 77843, USA. vsharma@tamu.edu.
Chemical Society reviews
|October 19, 2023
概括
单原子催化剂 (SAC) 为水处理中先进的氧化过程 (AOP) 提供了一种新的方法. 可以调整SAC以产生选择性反应物种,克服复杂水矩阵中传统AOP的局限性.
科学领域:
- 环境化学环境化学
- 材料科学 材料科学 材料科学
- 催化剂是一种催化剂.
背景情况:
- 全球水资源短缺需要先进的水处理解决方案.
- 传统的水处理系统在复杂的基质 (高离子,天然有机物质) 中与低度污染物作斗争.
- 先进的氧化过程 (AOPs) 产生用于污染物降解的活性物种.
研究的目的:
- 审查单原子催化剂 (SAC) 在处理水的AOP中的应用.
- 探索SACs激活的AOP的机制方面,并将其与传统AOP进行比较.
- 突出SAC在处理复杂水矩阵中的优势.
主要方法:
- 对过氧化和硫酸盐激活中的SACs现有文献的审查.
- 通过SACs生成反应性物种的机制性途径的分析.
- 激进与非激进物种选择性和稳定性在现实水中的比较.
主要成果:
- SACs可以激活过氧化物以产生反应性物种,包括基 (硫酸盐,) 和非基 (单氧,高价值金属).
- 可以设计SAC来选择性地产生非激进物种,这些物种不受水矩阵组件 (离子,NOM) 的影响.
- 使用SAC的非激进主导AOP显示出高效率和对复杂水处理的最小干扰.
结论:
- 适当设计的SAC是净化水的有效催化剂,提供高效率.
- 与传统的AOP相比,SAC提供了显著的优势,因为它最大限度地减少了复杂水成分的干扰.
- SAC代表了实现水资源可持续性目标的有希望的技术.
相关概念视频
Catalysis
27.0K
The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
27.0K
Radical Reactivity: Overview
2.1K
Radicals, the highly reactive species, gain stability by undergoing three different reactions. The first reaction involves a radical-radical coupling, in which a radical combines with another radical, forming a spin‐paired molecule. The second reaction is between a radical and a spin‐paired molecule, generating a new radical and a new spin‐paired molecule. The third reaction is radical decomposition in a unimolecular reaction, forming a new radical and a spin‐paired...
2.1K
Radical Reactivity: Nucleophilic Radicals
2.1K
Radicals adjacent to electron-donating groups are called nucleophilic radicals. These radicals readily react with electrophilic alkenes. The SOMO–LUMO interactions are the driving force for the reaction, where the high-energy SOMO of the electron-rich, nucleophilic radicals interacts with the low-energy LUMO of the electron-deficient, electrophilic alkenes. Such SOMO–LUMO interactions are the basis of reactive radical traps, affecting the selectivity in radical reactions. For...
2.1K
Radical Formation: Homolysis
3.6K
A bond is formed between two atoms by sharing two electrons. When this bond is broken by supplying sufficient energy, either two electrons can be taken up by one atom forming ions by the cleavage called heterolysis, or the two electrons are shared by two atoms, with one each creating radicals by the cleavage called homolysis.
3.6K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.3K
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
3.3K
Radical Autoxidation
2.2K
The oxidation of an organic compound in the presence of air or oxygen is called autoxidation. For example, cumene reacts with oxygen to form hydroperoxide. Autoxidation involves initiation, propagation, and termination steps. Many organic compounds are susceptible to autoxidation—especially ethers in the presence of oxygen, which form hydroperoxides. Even though this reaction is slow, old ether bottles contain small amounts of peroxide, which leads to laboratory explosions during ether...
2.2K


