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相关概念视频

Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

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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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Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

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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...
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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...
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Polymer Classification: Architecture01:14

Polymer Classification: Architecture

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Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
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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...
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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...
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脱聚合基塑化如何影响聚 (P-Dioxanone) 中冷结晶的过程

Roman Svoboda1, Jana Machotová2

  • 1Department of Physical Chemistry, Faculty of Chemical Technology, University of Pardubice, Studentská 573, Pardubice, 53210, Czech Republic.

Macromolecular rapid communications
|June 26, 2024
PubMed
概括

150°C以上的p-dioxanone的自塑化显著改变了其结晶和热特性. 这一过程影响了聚合物链的移动性,晶体的生长和机械特性.

关键词:
结晶化 结晶化的过程.脱聚合脱聚合的过程不同扫描热量计差异扫描热量计.聚二安是一种多氧化.自己塑化自塑化.

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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
  • 结晶研究 结晶研究

背景情况:

  • 自塑化,通过单体纳入增加聚合物链的流动性,影响聚合物的特性.
  • 聚二氧化 (PDX) 是一种聚合物,其结构,热和机械特性可以通过自我塑化而受到影响.

研究的目的:

  • 调查热诱导的自我塑性化对聚二氧化结晶的影响.
  • 分析由于自我塑化而导致的晶体生长从无形和化状态的变化.

主要方法:

  • 不同扫描热量计 (DSC)
  • 光学显微镜和拉曼显微镜
  • 热力学分析 (TMA) 是一种方法.
  • 使用多角度光散射 (SEC-MALS) 进行尺寸排除色谱.
  • 进行X射线衍射分析 (XRD).

主要成果:

  • 在150°C以上 (脱聚合温度) 观察到PDX结晶和机械性质的显著变化.
  • 强烈的自我塑化降低了结晶温度,增加了晶体生长率,消除了多态过渡,降低了化温度.
  • 自塑化并没有显著改变结晶体的大小,定位或形态,这些主要取决于晶体生长温度.

结论:

  • 在高于150°C的温度下,热诱导的自我塑化会对PDX结晶行为和热性能产生深远的影响.
  • 该研究讨论了可变激活能概念在观察到的结晶数据中的表现.