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

Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.6K
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...
3.6K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.4K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.4K
Types of Step-Growth Polymers: Polyesters01:20

Types of Step-Growth Polymers: Polyesters

2.3K
The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
2.3K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

8.1K
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.
8.1K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.3K
Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
2.3K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

2.8K
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...
2.8K

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

Driver wavelength and intensity dependence of extreme ultraviolet emission from laser-produced tin microdroplet plasmas.

Optics express·2026
Same author

Elemental Selenium/Tellurium in Polymer Assemblies: Responsive Innovation.

Polymer science & technology (Washington, D.C.)·2026
Same author

Dynamic Covalent Se─Se Bonds Enable Mechanically Adaptive Selenium Crystals.

Angewandte Chemie (International ed. in English)·2026
Same author

Polymer Shape Morphing Based on Dynamic Chemistries.

ACS applied materials & interfaces·2026
Same author

Recyclable thermoplastic silicone elastomers from non-carbon heteroatomic polymer backbones.

Nature communications·2026
Same author

Biomimetic Polymerization of Tellurocysteine: Breaking the Natural Amino Acid Radioprotection Limitation.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

相关实验视频

Updated: Sep 9, 2025

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst
07:39

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst

Published on: June 8, 2016

9.6K

通过可见光诱导的相位进化实现聚合物材料的机械进化

Cheng Liu1, Chaowei He1, Xiaobin Dai2

  • 1Key Lab of Organic Optoelectronic & Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing, 100084, China.

Advanced materials (Deerfield Beach, Fla.)
|September 3, 2025
PubMed
概括

这项研究引入了一种创建"进化"聚合物材料的新方法,该材料随着时间的推移动态地增强其机械性能. 这一突破允许对材料性能进行前所未有的控制, 模仿人工系统中的生物进化.

关键词:
在现场聚合机械进化阶段演变基可见光的反应性

更多相关视频

Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering
06:16

Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering

Published on: December 21, 2017

5.8K
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

11.9K

相关实验视频

Last Updated: Sep 9, 2025

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst
07:39

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst

Published on: June 8, 2016

9.6K
Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering
06:16

Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering

Published on: December 21, 2017

5.8K
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

11.9K

科学领域:

  • 材料科学
  • 聚合物化学
  • 机械工程

背景情况:

  • 人工聚合物材料通常是静态的,缺乏生物组织的动态,进化的特征.
  • 设计具有时间增强性质的聚合物仍然是材料科学的重大挑战.

研究的目的:

  • 提出并展示一种创建具有持续时间转换和增强机械性能的聚合物材料的策略.
  • 研究一种在人工聚合物系统中实现"机械进化"的方法.

主要方法:

  • 为设计具有时间可变相和机械性能的聚合物材料制定了一项策略.
  • 用可见光启动的现场聚合用于控制相位过渡的序列 (生成,分离,融合).
  • 该方法应用于水凝系统,以量化机械性质的变化.

主要成果:

  • 聚合物阶段经历了连续的转变,随着时间的推移导致机械性能明显显著改善.
  • 在水凝系统中实现了超过2400倍的Young模量创纪录的增加 (从18.5kPa到44.5MPa).
  • 使用可见光精确控制了机械性能的时间演变.

结论:

  • 拟议的策略允许设计具有暂时增强机械性能的人工聚合物材料,类似于生物进化.
  • 这项工作为根据需求量身定制材料特性和构建具有可调节,多层模块和复杂架构的先进超材料开辟了道路.