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相关概念视频

Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.9K
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...
2.9K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

3.0K
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...
3.0K
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
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
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

4.1K
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...
4.1K
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

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相关实验视频

Updated: Mar 3, 2026

Forming Giant-sized Polymersomes Using Gel-assisted Rehydration
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Forming Giant-sized Polymersomes Using Gel-assisted Rehydration

Published on: May 26, 2016

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超高分子量聚合物凝在水性介质中使用黄瓜[8]uril辅助激素聚合.

Élise Ansart1, Rebekka Hosch1, Mark W Tibbitt1

  • 1Macromolecular Engineering Laboratory, Department of Mechanical and Process Engineering, ETH Zurich, Sonneggstrasse 3, 8092 Zurich, Switzerland.

Macromolecules
|March 2, 2026
PubMed
概括

研究人员开发了一种简单的方法,使用宿主-客人化学制造超高分子量 (UHMW) 聚合物. 这种技术增强了自由基聚合 (FRP) 用于生产先进的聚合物材料和水凝.

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

背景情况:

  • 超高分子量 (UHMW) 聚合物由于链纠而表现出优越的特性.
  • 传统的自由基聚合 (FRP) 难以低启动效率和可重复性HMW聚合物合成.

研究的目的:

  • 开发一种可控的FRP方法来合成HMW聚合物.
  • 为了研究调节激素聚合的宿主-客人相互作用.
  • 为了生产HMW聚合物,这些聚合物在现场形成水凝.

主要方法:

  • 利用Cucurbit[8]uril (CB[8]) 和热启动器VA-044之间的宿主-客人相互作用来控制激素度.
  • 研究了烯胺 (AAm) 聚合,并将该策略应用于其他水溶性单体.
  • 进行了风湿学分析,以表征水凝的特性.

主要成果:

  • 成功合成了高频波聚合物,高达5.5MDa.
  • 从合成的UHMW聚合物中证明了在现场的水凝形成.
  • 观察到3MDa以上的水凝硬度增加和独立于频率.

结论:

  • 主客化学提供了一种简单有效的方法,通过FRP生产HMW聚合物.

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  • 这种方法可以轻松访问水性介质中的UHMW聚合物和水凝.
  • 最少添加CB[8]宏循环可显著改善标准FRP程序.