稀释反应性化合物的电化学价值化为氨:催化和反应性分离的进展
Wonjun Lee1,2, DongYeon Kim3, Kwiyong Kim2,4
1Department of Environmental Engineering, Jeju National University, Jeju Special Self-Governing Province, 63243, Republic of Korea.
ChemSusChem
|December 6, 2024
概括
本综述探讨了用于将稀释化合物转化为氨的催化剂和分离技术. 它详细介绍了从废物流中进行可扩展,节能高效的利用的途径.
科学领域:
- 环境化学环境化学
- 催化剂是一种催化剂.
- 化学工程是化学工程的重要组成部分.
背景情况:
- 全球对可持续管理的需求日益增长.
- 在有效地将稀释化合物 (酸盐,氧化) 转化为氨的挑战.
- 需要创新的解决方案来利用废物流中的.
研究的目的:
- 对低度活性物种的创新催化剂设计进行审查.
- 探索用于电化学价值化的先进分离和度技术.
- 检查与催化直接集成的反应分离策略.
主要方法:
- 对同质和异质催化剂设计的审查.
- 分析诸如电吸和透析之类的分离技术.
- 综合反应分离和催化过程的检查.
主要成果:
- 针对稀物种量身定制的催化剂的识别.
- 通过先进的分离来克服大众运输限制的演示.
- 概述了回收过程与催化物的直接整合.
结论:
- 从废中获得可扩展和节能生产氨的途径.
- 解决价值化中的关键挑战.
- 可持续管理中的工业应用前景.
相关概念视频
Overview of Nitrogen Metabolism
7.8K
Nitrogen is a very important element for life because it is a major constituent of proteins and nucleic acids. It is a macronutrient, and in nature, it is recycled from organic compounds and stored in the form of ammonia, ammonium ions, nitrate, nitrite, or nitrogen gas by many metabolic processes. Many of these metabolic processes are carried out only by prokaryotes.
The largest pool of nitrogen available in the terrestrial ecosystem is gaseous nitrogen (N2) from the air, but this...
The largest pool of nitrogen available in the terrestrial ecosystem is gaseous nitrogen (N2) from the air, but this...
7.8K
Metabolism of Chemolithotrophs
2
Chemolithotrophs are microorganisms that obtain energy by oxidizing inorganic molecules such as hydrogen gas (H₂), ammonia (NH₃), reduced sulfur compounds (H₂S, S²⁻), and ferrous iron (Fe²⁺). Unlike heterotrophic organisms that rely on organic carbon, chemolithotrophs transfer electrons from these inorganic donors to the electron transport chain (ETC), generating a proton motive force (PMF) that drives ATP synthesis through oxidative phosphorylation.
2
Preparation of Amines: Alkylation of Ammonia and Amines
3.2K
Alkylation is one of the methods used to prepare amines. Direct alkylation of ammonia or a primary amine with an alkyl halide gives polyalkylated amines along with a quaternary ammonium salt through successive SN2 reactions. This process of making the quaternary salt through the direct alkylation method is called exhaustive alkylation.
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
3.2K
Preparation of Amines: Reduction of Oximes and Nitro Compounds
3.4K
Oximes can be reduced to primary amines using catalytic hydrogenation, hydride reduction, or sodium metal reduction. The reduction of aliphatic and aromatic nitro compounds to primary amines takes place by either catalytic hydrogenation or by using active metals like Fe, Zn, and Sn in the presence of an acid.
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
3.4K
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
3.2K
Nitrous acid and nitric acids are two types of acids containing nitrogen, among which nitrous acid is weaker than nitric acid. Nitrous acid with a pKa value of 3.37 ionizes in water to give a nitrite ion and the hydronium ion.
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
3.2K
Preparation of Amines: Reductive Amination of Aldehydes and Ketones
2.7K
Carbonyl compounds and primary amines undergo reductive amination first to produce imines, followed by secondary amines in the same reaction mixture, using selective reducing agents like sodium cyanoborohydride or sodium triacetoxyborohydride. Reductive amination produces different degrees of substitution of amines depending on the starting amine substrate.
2.7K


