在加热过程中,半晶乙烯基离子体的结构变化
Shunsuke Murayama1, Go Matsuba1
1Graduate School of Organic Materials Science, Yamagata University, 4-3-16 Jonan, Yonezawa 992-8510, Japan.
Polymers
|January 11, 2025
概括
用不同的Zn/Na比率加热以乙烯为基础的离子体,揭示了离子聚合物和晶体结构的变化. 最佳的离子比率最大限度地提高了融度,显示联合的离子存在有利于晶体的生长.
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
- 物理化学 物理化学
背景情况:
- 基于半晶体乙烯的离子体具有影响材料性质的离子聚合物.
- 了解这些聚合物的热行为对于材料应用至关重要.
研究的目的:
- 在加热后研究以乙烯为基础的离子体中的离子聚合物的结构演变.
- 为了确定不同 (Zn) 和 (Na) 离子比对离子体热性质和微观结构的影响.
主要方法:
- 差分扫描热量计 (DSC) 用于热过渡和化行为.
- 在现场广角X射线散射 (WAXS) 观察温度依赖的晶体结构变化.
- 小角度X射线散射 (SAXS) 使用Yarusso-Cooper方程来分析离子聚合物尺寸.
主要成果:
- 点在很大程度上不受/比的影响,但热量在特定比率 (3:7和5:5) 上达到峰值.
- WAXS 显示,单质晶体在完全融化之前,会融化并重新结晶成形状.
- 萨克斯表示的离子聚合物在聚乙烯晶体化时会膨胀,这通常会压缩它们.
结论:
- /离子比率显著影响以乙烯为基础的离子体中的化和结晶体增长.
- 温度诱导的结构转变涉及明显的晶体相变化和离子聚合物的重新排列.
- 聚乙烯晶体化决定了观测到的离子聚合物的膨胀,影响了材料的整体行为.
相关概念视频
Polymer Classification: Crystallinity
2.8K
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...
2.8K
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
Polymer Classification: Architecture
2.6K
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...
2.6K
Phase Transitions: Melting and Freezing
12.3K
Heating a crystalline solid increases the average energy of its atoms, molecules, or ions, and the solid gets hotter. At some point, the added energy becomes large enough to partially overcome the forces holding the molecules or ions of the solid in their fixed positions, and the solid begins the process of transitioning to the liquid state or melting. At this point, the temperature of the solid stops rising, despite the continual input of heat, and it remains constant until all of the solid is...
12.3K
Thermal Electrocyclic Reactions: Stereochemistry
2.0K
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
2.0K
Strength and Heat of Hydration
210
The hydration of cement is an exothermic reaction in which heat is generated as cement hydrates. This heat of hydration is critical to cement's strength development. The rate at which this heat is generated affects the temperature rise, with a majority of the heat being released early in the hydration process, half within the first three days, and about 75% within the first week.
The heat of hydration for each cement compound is significant; for instance, tricalcium aluminate (C3A) and...
The heat of hydration for each cement compound is significant; for instance, tricalcium aluminate (C3A) and...
210


