用烯酸和芬顿的发起者移植粉:选择性挑战
Inge-Willem Noordergraaf1, Judy R Witono2, Hero J Heeres1
1Faculty of Science and Engineering, Green Chemical Engineering, Groningen University, Nijenborgh 4, 9747 AG Groningen, The Netherlands.
Polymers
|January 23, 2024
概括
使用Fenton的启动器将烯酸聚合在粉上,通过逐渐的单体添加显示出更好的选择性. 这种方法提高了潜在的工业应用的接种效率和材料特性.
科学领域:
- 聚合物化学 聚合物化学
- 材料科学 材料科学 材料科学
- 生物聚合物修饰修饰
背景情况:
- 在粉上进行移植聚合,为具有量身定制性质的新材料提供了一条途径.
- 芬顿的化学 (Fe2+/H2O2) 是一种具有成本效益的移植聚合的启动剂,但在烯酸中面临选择性挑战.
- 了解影响移植选择性的因素对于优化粉修饰至关重要.
研究的目的:
- 与其他系统相比,审查和解释与芬顿的启动器和烯酸观察到的较低的移植选择性.
- 提出一种基于反应工程的方案,以阐明移植选择性的差异.
- 评估在粉-烯酸系统中改善移植选择性的方法.
主要方法:
- 文献综述和对对接种聚合系统的现有数据的分析.
- 开发一个反应工程方案来解释选择性差异.
- 在批量反应器中使用凝化麻粉进行逐渐单体剂量的实验评估.
主要成果:
- 较低的移植选择性归因于较少的选择性粉激活和较高的初始单体-粉比率.
- 较少水溶性单体在实现更高的移植选择性方面具有优势.
- 渐进的单体剂量显著改善了麻豆粉的移植百分比 (17%至29%) 和移植选择性 (18%至31%).
结论:
- 逐渐的单体剂量代表了提高粉移植聚合选择性与芬顿的启动器的主要突破.
- 这些发现为优化粉修饰过程提供了基础.
- 为了完善方法和扩展到连续反应堆,需要进一步的研究.
相关概念视频
Anionic Chain-Growth Polymerization: Overview
2.1K
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
2.1K
Cationic Chain-Growth Polymerization: Mechanism
2.3K
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
2.3K
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
18.0K
The Fischer esterification reaction was developed by the German chemist Emil Fischer in 1895. It is a condensation reaction between carboxylic acids and alcohols in an acidic medium to give esters and water.
18.0K
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
7.9K
Carboxylic acids react with alcohols to yield esters via an acid-catalyzed condensation reaction called Fischer esterification. This is a nucleophilic acyl substitution reaction that proceeds via a tetrahedral intermediate, where a water molecule is eliminated as the leaving group.
7.9K
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
2.9K
Hydrolysis of esters under acidic conditions proceeds through a nucleophilic acyl substitution. In the presence of excess water, the reaction proceeds in a reversible manner, forming carboxylic acids and alcohols.
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
2.9K
Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene
7.1K
The Friedel–Crafts acylation reactions involve the addition of an acyl group to an aromatic ring. These reactions proceed via electrophilic aromatic substitution by employing an acyl chloride and a Lewis acid catalyst such as aluminum chloride to form aryl ketone.
7.1K


