含有双二二部分的聚碳酸盐的合成和高热老化
Tao Lu1, Wei Fang1, Qian Zhou1
1Shanghai Key Laboratory of Advanced Polymeric Materials, School of Materials Science and Engineering, East China University of Science and Technology Shanghai 200237 China wgz@ecust.edu.cn.
RSC advances
|June 4, 2024
概括
从BNE和BPEF单体合成的新聚碳酸盐表现出增强的水解稳定性和对物理衰老的抗性. 这些先进材料在湿热条件下提供了更好的性能,这对于苛刻的应用至关重要.
科学领域:
- 聚合物化学 聚合物化学
- 材料科学 材料科学 材料科学
- 光学材料 光学材料
背景情况:
- 聚碳酸盐被广泛使用,但在高热压力下可以降解.
- 开发具有增强稳定性和光学性能的聚碳酸对于先进的应用至关重要.
研究的目的:
- 合成和表征具有高折射率,低双折射率和优异的高热阻力的新型聚碳酸盐.
- 研究这些共聚合物的单体结构,水解稳定性和物理衰老之间的关系.
主要方法:
- 2,2'-bis[4-]2-hydroxyethoxy) -1,1'-binaphthyl (BNE) 和9,9-bis[4-]2-hydroxyethoxy) phenyl]fluorene (BPEF) 的联合聚合. 这两种聚合物中,二氧化和二氧化是最常见的.
- 对双甲基聚碳酸盐的水解稳定性的比较分析.
- 在干燥和湿热条件下的物理衰老现象的评估,使用输热量损失测量.
- 物理衰老与玻璃过渡温度 (Tg) 的相关性.
主要成果:
- 与双甲聚碳酸相比,BNE-BPEF共聚合物显著改善了水解稳定性.
- 在酸性热条件下,BNE和BPEF单体的pKa值较高有助于降低体水解.
- 物理衰老,以热损失表示,与衰老温度和Tg.之间的差异线性相关.
- 较低的Tg导致更明显的物理衰老和延伸强度/模块的增加,而较高的Tg减轻了衰老.
结论:
- BNE和BPEF的共聚化产生了具有出色的水解稳定性和可调整的物理衰老行为的聚碳酸盐.
- 增强的稳定性与单体性质和降低对水解的敏感性有关.
- 玻璃过渡温度是控制这些聚碳酸的物理老化和机械性质变化的关键因素.
更多相关视频
相关概念视频
Types of Step-Growth Polymers: Polyesters
2.2K
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...
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...
2.2K
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
Step-Growth Polymerization: Overview
3.4K
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...
Many natural and synthetic polymers are produced by...
3.4K
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


