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相关概念视频

Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

2.9K
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...
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Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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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...
3.5K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

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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...
2.2K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.3K
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...
2.3K
Polymers02:34

Polymers

35.8K
The word polymer is derived from the Greek words “poly” which means “many” and “mer” which means “parts”. Polymers are long chains of molecules composed of repeating units of smaller molecules, known as monomers. They either occur naturally, such as DNA and proteins, or can be constructed synthetically, like plastics. They have varied structural characteristics, such as linear chains, branched chains, or complex networks, that contribute to the...
35.8K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.0K
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...
2.0K

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相关实验视频

Updated: Jul 5, 2025

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

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在聚合物复合模型中,自我组装和相分离之间的相互作用.

Tianhao Li1, W Benjamin Rogers2, William M Jacobs1

  • 1Department of Chemistry, Princeton University, Princeton, New Jersey 08544, USA.

Physical review. E
|January 20, 2024
PubMed
概括
此摘要是机器生成的。

我们开发了一个模型,展示了如何将聚合物链组装成复合体可以防止相位分离. 这种理论方法揭示了复杂的相位行为,与典型的聚合物溶液不同.

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

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Assembly and Characterization of Polyelectrolyte Complex Micelles
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科学领域:

  • 物理化学 物理化学
  • 聚合物科学 聚合物科学
  • 理论化学 理论化学

背景情况:

  • 聚合物溶液可以由于有吸引力的聚合物-聚合物相互作用而经历相分离.
  • 聚合物的聚合,聚合物链的组装成复合物,可以影响或抑制相位分离.

研究的目的:

  • 开发一个理论模型,预测聚合物溶液的相位行为,其中相位分离与寡合化竞争.
  • 为了研究固体测量复合体形成如何影响聚合物溶液相位图.

主要方法:

  • 将统计关联流体理论 (SAFT) 与自组装的两种状态模型相结合.
  • 开发用于导出系统特定阶段图的图形方法.

主要成果:

  • 该模型预测了丰富的相位行为,包括重新进入的相位过渡.
  • 证明复杂的形成可以导致相图质量上与典型的高分子溶液与较低的临界溶液温度质量上不同.

结论:

  • 氧化和相分离之间的相互作用导致聚合物溶液中的复杂和独特的相位行为.
  • 理论模型为理解和预测这些现象提供了一个框架,为自我组装影响宏观性质的系统提供了洞察力.