Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

2.6K
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
2.6K
Polymer Classification: Architecture01:14

Polymer Classification: Architecture

4.0K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
4.0K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

3.7K
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this species into...
3.7K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

3.6K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
3.6K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

10.0K
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.
10.0K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

4.5K
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...
4.5K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Chain collapse and dynamics of inhomogeneities in aqueous solutions of poly(<i>N</i>-isopropylacrylamide) and its block copolymers with polyethylene glycol.

Physical chemistry chemical physics : PCCP·2026
Same author

Polymer Systems with Correlated Activity: Stars Versus Linear Chains.

Molecules (Basel, Switzerland)·2025
Same author

Novel Hydroxyl-Functional Aliphatic CO<sub>2</sub>-Based Polycarbonates: Synthesis and Properties.

International journal of molecular sciences·2025
Same author

The Potential for Reusing Superabsorbent Polymer from Baby Diapers for Water Retention in Agriculture.

Gels (Basel, Switzerland)·2025
Same author

How to control a polymer conformation using active forces and sequence design.

The Journal of chemical physics·2025
Same author

Kinetics of Carboxylic Acids Formation During Polypropylene Thermooxidation in Water Saturated with Pressurized Oxygen.

Polymers·2025

相关实验视频

Updated: Mar 4, 2026

Facile and Efficient Preparation of Tri-component Fluorescent Glycopolymers via RAFT-controlled Polymerization
10:54

Facile and Efficient Preparation of Tri-component Fluorescent Glycopolymers via RAFT-controlled Polymerization

Published on: June 19, 2015

10.2K

通过极端聚合,具有分支结构的宏分子:从计算机模拟的洞察力.

Konstantin O Borodin1,2, Artem V Sergeev1,2, Elena Yu Kozhunova1,3

  • 1Lomonosov Moscow State University, Faculty of Physics, Moscow 119991, Russia.

The Journal of chemical physics
|March 3, 2026
PubMed
概括

这项研究开发了一种分子动力学模型,用于使用基极聚合 (RP) 的分支聚合物合成. 增加链转移剂 (CTA) 含量会转移凝,从而形成高分子量分枝聚合物.

更多相关视频

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
06:49

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

Published on: April 22, 2016

12.5K
Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

8.4K

相关实验视频

Last Updated: Mar 4, 2026

Facile and Efficient Preparation of Tri-component Fluorescent Glycopolymers via RAFT-controlled Polymerization
10:54

Facile and Efficient Preparation of Tri-component Fluorescent Glycopolymers via RAFT-controlled Polymerization

Published on: June 19, 2015

10.2K
Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
06:49

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

Published on: April 22, 2016

12.5K
Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

8.4K

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
  • 计算化学计算化学

背景情况:

  • 分支聚合物具有可调节的特性,但很难通过常规的基极聚合 (RP) 来合成具有所需特性的聚合物.
  • 缺乏对RP期间控制宏分子架构的系统研究.

研究的目的:

  • 开发一个计算模型来模拟使用RP的分支聚合物形成.
  • 研究交叉连接剂 (CL) 和链转移剂 (CTA) 度对聚合物结构和可溶性的影响.

主要方法:

  • 使用基于克雷默-格雷斯特框架的三维粗粒度分子动力学模型.
  • 模拟包含了随机反应,包括启动,传播,交联,链转移和终止.
  • 用基于图形的分解和碎形维度计算分析了宏分子架构.

主要成果:

  • 根据CTA含量确定了两个不同的聚合模式.
  • 低CTA含量导致了早期凝和网络主导的系统.
  • 增加的CTA含量将凝转移到更高的转换,促进高分子量分支聚合物的可溶性分量.
  • 发现了 [CL] = 2 [CTA] 的最佳条件,以实现高转化凝,产生可溶性分支巨分子.

结论:

  • 该研究提供了使用标准RP合成可溶性分枝聚合物的定量指导.
  • 对试剂比率 (CL和CTA) 的控制对于定制聚合物架构和实现所需性能至关重要.