在气相中的烯的电氧化与固体-聚合物-电解质水电解
Minori Saito1, Yuta Kojima1, Shoji Iguchi1,2
1Department of Chemical Science and Engineering, Tokyo Institute of Technology, Meguro 152-8552, Japan.
ACS applied materials & interfaces
|November 26, 2024
概括
使用无溶剂,无素的电氧化系统,实现了烯直接氧化为氧化物 (PO). 通过优化PtOx阳极和水扩散,轻度热压提高了PO形成率和法拉第效率.
科学领域:
- 电化学 电化学 电化学
- 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:
- 烯直接氧化成氧化物 (PO) 对于化学合成至关重要.
- 目前的方法往往涉及恶劣的条件或危险的试剂.
- 开发高效和可持续的环氧化系统仍然是一个关键的挑战.
研究的目的:
- 开发一种新的,无溶剂的反应系统,用于直接气相电氧化到PO.
- 为了研究阳极表面在环氧化过程中的作用.
- 优化反应条件,以提高PO产量和效率.
主要方法:
- 使用固体聚合物电解液 (SPE) 电解用于气相电氧化.
- 采用了氧化 (PtOx) 阳极,这对于反应至关重要.
- 进行间隔电解实验,研究PO积累和氧化.
- 为了优化,将温和的热压条件应用于SPE单元.
主要成果:
- 通过使用水作为氧化剂,成功实现了烯到PO的直接气相电氧化.
- 确定氧化PtOx阳极表面对于环氧化和氧化都至关重要.
- 在阳极上观察到PO的顺序氧化和积累.
- 证明温和的热压能提高PO形成率和法拉第效率 (FE).
- 在最佳条件下,在SPE (Nafion) 膜内提高水的扩散性.
结论:
- 开发的SPE电解系统为氧化生产提供了一个有前途的无素路线.
- 优化SPE单元条件,如温和的热压,对于提高催化活性和效率至关重要.
- 需要进一步的研究来提高工业可行性的整体法拉第效率.
相关概念视频
Free-Radical Chain Reaction and Polymerization of Alkenes
7.7K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
7.7K
Preparation of Epoxides
7.4K
Overview
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of...
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of...
7.4K
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
5.6K
Diols are compounds with two hydroxyl groups. In addition to syn dihydroxylation, diols can also be synthesized through the process of anti dihydroxylation. The process involves treating an alkene with a peroxycarboxylic acid to form an epoxide. Epoxides are highly strained three-membered rings with oxygen and two carbons occupying the corners of an equilateral triangle. This step is followed by ring-opening of the epoxide in the presence of an aqueous acid to give a trans diol.
5.6K
Sharpless Epoxidation
3.8K
The conversion of allylic alcohols into epoxides using the chiral catalyst was discovered by K. Barry Sharpless and is known as Sharpless epoxidation. The use of a chiral catalyst enables the formation of one enantiomer of the product in excess. This chiral catalyst is mainly a chiral complex of titanium tetraisopropoxide and tartrate ester (specific stereoisomer). The stereoisomer used in the chiral catalyst dictates the formation of the enantiomer of the product. In other words, the use of...
3.8K
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
2.5K
Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
2.5K
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
8.3K
The rate of acid-catalyzed hydration of alkenes depends on the alkene's structure, as the presence of alkyl substituents at the double bond can significantly influence the rate.
8.3K


