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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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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
Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

2.4K
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...
2.4K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.5K
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
Polymer Classification: Architecture01:14

Polymer Classification: Architecture

2.7K
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...
2.7K
Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

1.9K
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...
1.9K

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相关实验视频

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Fabrication of Large-area Free-standing Ultrathin Polymer Films
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Fabrication of Large-area Free-standing Ultrathin Polymer Films

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在聚合物薄膜中的层次表面不稳定性

Belda Amelia Junisu1, Ya-Sen Sun2

  • 1Department of Chemical and Materials Engineering, National Central University, Taoyuan 32001, Taiwan.

Langmuir : the ACS journal of surfaces and colloids
|October 20, 2023
PubMed
概括

薄膜中的等级不稳定性,以明显的宏观,微观和中等尺度模式为特征,在高湿度下,在挥发性溶液的旋转涂层过程中出现. 这些复杂的薄膜结构受到溶剂挥发性和环境条件的影响,而不是薄膜特性.

科学领域:

  • 材料科学 材料科学 材料科学
  • 薄膜物理学 薄膜物理学
  • 表面化学 表面化学

背景情况:

  • 薄膜形态对于设备性能至关重要.
  • 了解薄膜形成期间的不稳定性是控制结构的关键.
  • 螺旋涂层是一种用于薄膜沉积的常见技术.

研究的目的:

  • 为了研究螺旋涂层薄膜中等级不稳定的形成.
  • 确定影响这些不稳定的发展的关键因素.
  • 阐明导致等级不稳定的潜在机制.

主要方法:

  • 具有不同挥发性的聚4-乙烯胺 (P4VP) 溶液的螺旋涂层.
  • 在旋转涂层过程中对相对湿度 (RH) 的控制变化.
  • 薄膜在宏观,微观和中等尺度上的形态特征.

主要成果:

  • 层次的不稳定性表现为类似风车的模式 (宏观),贝纳德细胞/条纹 (微观) 和洞 (中等).
  • 在高RH下,高挥发性溶剂 (甲醇/乙醇中的P4VP) 发生不稳定性.
  • 不稳定性被低挥发性溶剂 (P4VP在醇/布坦醇中) 抑制,不论RH.
  • 薄膜的特性,如分子量,度,旋转率和厚度,不会显著影响不稳定性形成.

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Procedure for the Transfer of Polymer Films Onto Porous Substrates with Minimized Defects
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Fabricating Reactive Surfaces with Brush-like and Crosslinked Films of Azlactone-Functionalized Block Co-Polymers
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结论:

  • 层次的不稳定性主要取决于溶剂挥发性和相对湿度.
  • 形成机制涉及贝纳德-马拉贡尼对流,水蒸气凝结和旋转涂层动力学.
  • 在旋转涂层过程中,可以通过操纵溶剂选择和环境条件来控制薄膜形态.