聚乙烯-尿素) 基弹性体的物理性质由齐格扎克键和可滑式交叉连接形成
Sojung Seo1, Jin-Woo Park2, Dong-Gyun Kim3
1Department of Materials Science and Engineering, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, Republic of Korea.
ACS macro letters
|November 3, 2023
概括
在这项研究中,使用齐克扎克的键和可滑动的交叉连接,增强了可拉伸的弹性体. 由此产生的聚乙氨酸弹性体会显著提高性和弹性,在重复变形下保持性能.
科学领域:
- 材料科学 材料科学 材料科学
- 聚合物化学 聚合物化学
- 机械工程 机械工程
背景情况:
- 开发高性能可拉伸弹性体对于先进的应用至关重要.
- 传统的弹性体通常在性,灵活性或耐久性方面面临限制.
- 需要新的分子设计来克服这些挑战.
研究的目的:
- 为了研究曲的结和可滑式交叉连接对弹性质特性的影响.
- 设计一种基于聚乙-尿素的新型可拉伸弹性体.
- 评估开发的弹性体的机械性能和耐用性.
主要方法:
- 在弹性体骨干中加入聚乙烯-尿素 (PET) 带有齐克扎克的气结合.
- 引入一个可滑动的聚甲交叉连接器.
- 机械测试包括性,弹性和循环变形在150%的应变下.
主要成果:
- 基于聚乙烯-尿素的弹性体显示出与线性聚乙烯甘醇相比的性高出14倍.
- 可滑动的聚甲交叉连接器使弹性体的灵活性翻了一番,而不是刚性聚合物交叉连接器.
- 弹性体在重复变形后保持其机械性能,直至150%的应变.
结论:
- 齐格扎克结和滑动交联是设计优质可拉伸弹性体的有效策略.
- 开发的聚乙氨酸弹性体提供了高性,灵活性和耐久性的有前途的组合.
- 这项工作为创建用于苛刻应用的先进材料提供了新的途径.
相关概念视频
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
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
Stability of Conjugated Dienes
3.4K
Introduction
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
3.4K
Molecular Weight of Step-Growth Polymers
2.2K
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...
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: 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...
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
Ziegler–Natta Chain-Growth Polymerization: Overview
3.3K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.3K


