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相关概念视频

Polymers02:34

Polymers

21.1K
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Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.1K
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,...
2.1K
Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

2.0K
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...
2.0K
Types of Step-Growth Polymers: Polyesters01:20

Types of Step-Growth Polymers: Polyesters

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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
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...
3.6K
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...
2.9K

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相关实验视频

Updated: Aug 21, 2025

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules
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Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules

Published on: April 28, 2014

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在ABC瓶块聚合物中的核心体

Shuquan Cui1, Bo Zhang2, Liyang Shen2

  • 1Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.

Journal of the American Chemical Society
|November 15, 2022
PubMed
概括

具有独特架构的瓶块共聚物使得更大,有序的网络材料成为可能. 这项研究报告了这些聚合物中的第一个双回旋网络形态,为先进材料特性铺平了道路.

科学领域:

  • 聚合物科学
  • 材料科学
  • 纳米技术

背景情况:

  • 区块聚合物自我组装可以创建具有可调节性质的3D周期网络,
  • 传统的线性块聚合物在有序网络大小和组装速度方面存在限制.
  • 瓶架构提供了扩展的骨干和更快的动态,克服了线性聚合物限制.

研究的目的:

  • 研究聚乙烯-乙烯-b-聚乙烯 (PEP-PS) 和PEP-PS-聚乙烯氧化物 (PEO) 瓶刷块共聚物的相位行为.
  • 探索瓶架构的潜力,以实现超越线性系统的新型网络形态.
  • 在AB瓶块共聚物中首次观察网络形态.

主要方法:

  • 使用环开放转化聚合物 (ROMP) 合成PEP-PS二块和PEP-PS-PEO三块瓶刷共聚物.
  • 使用小角度X射线散射 (SAXS) 描述共聚物相位行为.
  • 分析不同组合和脊柱聚合度的形态形成 (Nbb).

主要成果:

  • PEP-PS双块完全形成圆柱形和叶片形态.
  • 将PEO块添加到PEP-PS双块中,导致了显著的双回旋 (GYR) 阶段窗口.
  • GYR单元尺寸显示了对Nbb (d~Nbb^0.92) 的功率规律依赖,表明了可扩展性.

更多相关视频

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

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相关实验视频

Last Updated: Aug 21, 2025

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules
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Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules

Published on: April 28, 2014

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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

Published on: February 7, 2017

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

Published on: June 20, 2019

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结论:

  • 瓶三块共聚物可以形成复杂的3D网络形态,特别是双回形状.
  • 观察到的GYR尺寸与骨干长度的缩放表明,有可能创建比以前更大的网络结构.
  • 这项工作证明了ROMP化学在设计具有有序纳米结构的先进多块瓶聚合物的实用性.