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相关概念视频

Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

3.2K
Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
3.2K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

4.3K
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...
4.3K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.7K
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...
2.7K
Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

3.1K
Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
3.1K

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相关实验视频

Updated: Jan 15, 2026

Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning
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Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning

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通过单步沉聚合物合成的热敏共聚合物微凝:随机结构还是块结构?

Letizia Tavagnacco1,2, Elena Buratti3, Jacopo Vialetto4,5

  • 1CNR-ISC, Uos Sapienza, Piazzale A. Moro 2, Roma, 00185, Italy.

Small (Weinheim an der Bergstrasse, Germany)
|October 9, 2025
PubMed
概括

这项研究表明,热敏共聚合物微凝意外形成块状结构,而不是随机排列. 这一发现挑战了目前的理解,并提供了设计微凝的新方法,以定制材料的响应性.

关键词:
核磁共振光谱法 (NMR) 是一种光谱法.合作聚合的共聚合.微凝是一种微凝.分子建模分子建模有选择性的中子散射.

更多相关视频

Synthesis of PolyN-isopropylacrylamide Janus Microhydrogels for Anisotropic Thermo-responsiveness and Organophilic/Hydrophilic Loading Capability
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Synthesis of PolyN-isopropylacrylamide Janus Microhydrogels for Anisotropic Thermo-responsiveness and Organophilic/Hydrophilic Loading Capability

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Magnetic and Thermal-sensitive PolyN-isopropylacrylamide-based Microgels for Magnetically Triggered Controlled Release
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相关实验视频

Last Updated: Jan 15, 2026

Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning
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Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning

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Synthesis of PolyN-isopropylacrylamide Janus Microhydrogels for Anisotropic Thermo-responsiveness and Organophilic/Hydrophilic Loading Capability
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Magnetic and Thermal-sensitive PolyN-isopropylacrylamide-based Microgels for Magnetically Triggered Controlled Release
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科学领域:

  • 聚合物科学 聚合物科学
  • 材料科学 材料科学 材料科学
  • 软物质物理学 软物质物理学

背景情况:

  • 聚合物微凝对于响应性材料至关重要,但它们的内部结构很难解决.
  • 了解微凝架构是控制它们的响应和应用的关键.

研究的目的:

  • 描述热反应性多聚-N-异烯胺-co-N-异烯甲胺 (P(NIPAM-co-NIPMAM)) 共聚合物微凝的内部结构.
  • 为了研究这些微凝中的单体分布,并挑战随机排列的假设.

主要方法:

  • 综合实验技术:小角度中子散射 (SANS),动态光散射 (DLS) 和核磁共振 (NMR).
  • 先进的计算建模:微凝结构的多尺度和原子模拟.
  • 合成同位素标记的微凝进行详细分析.

主要成果:

  • 实验和模拟数据显示了单体的偏好区块式组织,与假定的随机分布相矛盾.
  • 13C-NMR证实了NIPAM丰富的块的存在.
  • 模拟将块架构与特定的局部结模式联系起来.

结论:

  • 这项研究提供了第一个直接证据,证明了P ((NIPAM-co-NIPMAM) 微凝中偏好的块形成.
  • 这项工作建立了一种可推广的方法,用于发现共聚物微凝中隐藏的结构秩序.
  • 这些发现为设计具有增强和控制响应性的微凝提供了新的策略.