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相关概念视频

Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

3.1K
Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
3.1K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.1K
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...
2.1K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.4K
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...
2.4K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.5K
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...
3.5K
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
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.2K
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,...
2.2K

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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在无形固体界面的聚合物核的热起源.

Ming Wang1,2, Zijian Song1,3, Guoming Liu1,2

  • 1Institute of Chemistry, Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Engineering Plastics, Chinese Academy of Sciences, Beijing 100190, China.

Physical review letters
|July 31, 2025
PubMed
概括

在接口处的聚合物结晶核形成是由弱相互作用时的链损失驱动的. 较强的相互作用有利于同质核形成,而不是表面诱导的聚合物结晶.

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Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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科学领域:

  • 聚合物科学 聚合物科学
  • 材料科学是一种材料科学.
  • 物理化学 物理化学

背景情况:

  • 接口显著影响物理,化学和生物过程.
  • 由于较低的核化屏障,聚合物结晶经常在固体接口 (异质核化) 开始.
  • 在接口附近的链形状和动力学与大批量有很大差异.

研究的目的:

  • 在聚合物中区分表面和同质核化机制.
  • 研究介面相互作用和聚合物链在核形成中的作用.

主要方法:

  • 利用纳米孔封闭系统研究聚合物核化.
  • 进行了全面的晶体方向分析,以区分核化场景.

主要成果:

  • 表面诱导的核形成主要受热效应的支配.
  • 这种热效应源于结构的丧失,因为聚合物链在弱相互作用的接口上变平.
  • 当界面相互作用强烈时,均质核变为主导.

结论:

  • 这项研究阐明了在聚合物中驱动表面与均核化的独特机制.
  • 界面能量和聚合物链形态是决定核化途径的关键因素.
  • 这些发现为通过接口工程控制聚合物结晶提供了洞察力.