解开反向化聚合物的整形学
Derek J Bischoff1, Taeheon Lee2, Kyung-Seok Kang2
1Department of Materials Science and Engineering, University of Delaware, Newark, DE, 19716, USA.
Nature communications
|November 21, 2023
概括
通过逆化合成高硫聚合物,可以通过单个放松时间来描述材料. 这一突破简化了聚合物融的整形学,为先进的应用提供了独特的马克斯威尔材料.
科学领域:
- 聚合物科学 聚合物科学
- 材料化学 材料化学
- 类风病学 类风病学 类风病学
背景情况:
- 大量聚合物化物表现出复杂的质行为,需要多次放松时间.
- 通过逆火山化合成的有机聚硫化物为简化粘弹性表征提供了一个独特的平台.
研究的目的:
- 通过逆化合成高硫含量的聚合物.
- 描述这些新型聚合物的质性质,并确定它们是否可以用单个放松时间来描述.
- 研究解离性键交换在它们粘弹性行为中的作用.
主要方法:
- 高硫聚合物的逆化合成 (≥50%重量%).
- 单频振荡式剪切体质学来测量应力放松.
- 时间-温度叠加构建修复学主曲线.
- 使用麦克斯韦粘性弹性模型进行分析.
主要成果:
- 合成的高硫含量 (≥50%重量%) 的聚合物,具有单个应力放松时间.
- 证明S-S债券中的离散性债券交换主导压力放松.
- 展示了麦克斯韦模型对这些离散的共价适应性网络和活体聚合物的适用性.
- 使用放松时间作为水平转移因子构建了学主曲线.
结论:
- 来自反硫化的高硫聚合物可以用单个放松时间来描述,从而简化了聚合物质学.
- 这些材料代表了马克斯韦尔材料的罕见实验实现.
- 这项研究提供了这种独特的聚合物材料类别的第一个全面的学特征.
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
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
2.6K
Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
2.6K
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
Olefin Metathesis Polymerization: Overview
2.1K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
2.1K
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


