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Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

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Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
2.2K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

4.3K
Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
4.3K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.8K
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...
2.8K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.4K
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
2.4K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

9.4K
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.
9.4K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.6K
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,...
2.6K

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Updated: Jan 17, 2026

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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使用流体化学了解聚甲酸的脱聚合动力学 (使用流体化学).

Leonard P M Göhringer1,2, Gayathri Dev Ammini1, Tanja Junkers1

  • 1Polymer Reaction Design Group, School of Chemistry, Monash University, 19 Rainforest Walk, Building 23, Clayton, VIC 3800, Australia. tanja.junkers@monash.edu.

Faraday discussions
|September 18, 2025
PubMed
概括
此摘要是机器生成的。

可逆添加-碎片化-链转移 (RAFT) 脱聚合是一种关键的化学回收方法. 这项研究确定了在连续流下RAFT脱聚变动力学,将透析确定为速度限制步骤.

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相关实验视频

Last Updated: Jan 17, 2026

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization

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Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
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科学领域:

  • 聚合物化学 聚合物化学
  • 化学工程是化学工程的重要组成部分.
  • 材料科学 材料科学 材料科学

背景情况:

  • 可逆添加碎片化链转移 (RAFT) 脱聚合使得聚合物能够有效地进行化学回收.
  • 在线透析的连续流过程可以加速脱聚合.
  • 了解动力学对于优化基于流量的聚合物回收利用至关重要.

研究的目的:

  • 在连续流条件下确定RAFT脱聚合的动力学.
  • 研究温度和聚合物度对脱聚合率的影响.
  • 为了确定流量RAFT脱聚合与直线透析的速度限制步骤.

主要方法:

  • 在连续流系统中研究了聚甲酸 (polyBMA) 的RAFT脱聚合.
  • 在120°C至160°C之间的多样化脱聚合温度.
  • 分析了脱聚合率对初始聚合物度的依赖性,并将其与透析清除率进行比较.

主要成果:

  • 确定RAFT脱聚合物的激活能量为79.5kJ mol-1.1.
  • 观察到脱聚合率对初始聚合物度的平方根依赖.
  • 确定了进流膜透析作为速度决定的步骤,比脱聚合速度慢得多.

结论:

  • 透析步骤是连续流动RAFT脱聚合与直线透析中的瓶.
  • 在透析中增加交叉流速加速了单体去除.
  • 优化透析条件对于使用RAFT有效的基于流量的聚合物回收是必不可少的.