侧组拓结构修改轨道和凝结状态特征增强了聚烯烯的电抗分解性能
Shixun Hu1, Cheng Tong1, Xiongjie Yang1
1Department of Electrical Engineering, Tsinghua University, Beijing, 100084, China. hejl@tsinghua.edu.cn.
Physical chemistry chemical physics : PCCP
|January 15, 2025
概括
将聚烯与乙乙烯 (VAc) 侧组进行修改,比N-乙-罗利 (NVP) 更能提高介电性能. 这是由于VAc造成的.
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
- 电气工程 电气工程
背景情况:
- 聚烯材料对于电绝缘和储能至关重要.
- 极端侧组的修改是提高其介电性能的一个关键策略.
- 了解侧组结构对材料特性的影响是必不可少的.
研究的目的:
- 为了研究极侧组拓结构对聚烯 (PP) 特性的影响.
- 分析对微观和宏观特征的影响,特别是电气抗分解能力.
- 为设计先进介电材料提供洞察力.
主要方法:
- 乙烯酸乙烯 (VAc) 和N-乙烯酸 (NVP) 的化学接种在聚烯上.
- 结晶和热性质的实验性表征.
- 计算分析包括深陷深度计算和分子动态 (MD) 模拟.
主要成果:
- 侧组拓显著影响PP的结晶和热性质.
- 与NVP移植的PP相比,VAc移植的PP显示出更深的陷轨道和更少的自由体积.
- 用VAc移植的PP表现出增强的分解强度 (在30°C时高达21%,在90°C时高达14%).
结论:
- 极端侧组的拓结构极大地影响介电性能.
- 较深的陷轨道和VAc移植的PP中较小的自由体积有助于更高的分解强度.
- 这项研究为优化电力设施中的介电材料提供了微观的理解.
相关概念视频
π Molecular Orbitals of 1,3-Butadiene
12.7K
Conjugated dienes have lower heats of hydrogenation than cumulated and isolated dienes, making them more stable. The enhanced stabilization of conjugated systems can be understood from their π molecular orbitals.
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
12.7K
Characteristics and Nomenclature of Homopolymers
4.3K
Polymers that are made up of identical monomer units are called homopolymers. Only one repeating unit is involved in the construction of the homopolymer structure. For example, as depicted in Figure 1, polypropylene is a homopolymer constituted of propylene monomers. Here, the only repeating unit in the polymer chain is propylene.
4.3K
Polymer Classification: Architecture
4.1K
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...
4.1K
Polymer Classification: Crystallinity
4.3K
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...
4.3K
Polymer Classification: Stereospecificity
3.4K
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...
3.4K
Types of Step-Growth Polymers: Polyesters
2.7K
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 polymer...
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 polymer...
2.7K


