生物基亚利发性聚合物的中二醇重复单元对热和拉伸性能的影响
Kanoko Isami1, Gaku Miyamoto1, Mohamed Mehawed Abdellatif1
1Department of Chemistry, Tokyo Metropolitan University, 1-1 Minami Osawa, Hachioji, Tokyo 192-0397, Japan.
ACS omega
|March 2, 2026
概括
来自植物资源的生物基聚烯提供易于回收和可调节的性能. 使用10-无酸和异曼胺二醇的聚合物表现出优越的抗拉强度和延伸性,性能优于现有材料.
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
- 可持续化学 可持续化学
背景情况:
- 生物基亚利发性聚合物是从可再生资源中提取的.
- 单体设计显著影响聚的特性和可回收性.
- 非食用植物来源为聚单体提供可持续的途径.
研究的目的:
- 为了合成和表征从10-undecenoic酸和各种二醇的新生物基聚烯.
- 研究二醇结构对热和机械性能的影响.
- 评估这些聚的潜力,作为高性能材料.
主要方法:
- 使用了亚环二烯转化酶 (ADMET) 聚合.
- 随后进行了合化以达到和.
- 分析了热性质 (例如,玻璃过渡温度).
- 测量了聚合物薄膜的拉伸性能 (应力,应变,屈服强度).
主要成果:
- 包含异曼尼德 (IM) 或L-三醇 (LTh) 二醇的聚合物根据二醇部分表现出不同的热性能.
- 当LTh或IM单位被二碳酸连接在一起时,无形聚合物形成.
- 聚合物P7和HP7,由10-无烯酸和IM通过转-1,4-环合素二碳酸衍生而成,表现出极好的拉力应力和拉力.
- 这些聚合物与现有的IM或基于异酸的聚合物相比,具有更高的机械性能.
- 含有2,5-二氧化酸的聚合物表现出脆脆的骨折.
结论:
- 单体设计,特别是二醇成分,对生物基聚烯的特性进行了严格的控制.
- 使用10-无酸和异曼尼德合成的聚合物为材料应用提供了有前途的机械性能.
- 双碳酸链接剂的选择影响了聚合物的热和机械行为,而转-1,4-环二碳酸产生了优异的结果.
相关概念视频
Types of Step-Growth Polymers: Polyesters
2.6K
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...
2.6K
Polymer Classification: Architecture
4.0K
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...
4.0K
Polymer Classification: Stereospecificity
3.3K
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...
3.3K
Free-Radical Chain Reaction and Polymerization of Alkenes
10.0K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
10.0K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
2.3K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
2.3K
Olefin Metathesis Polymerization: Overview
2.7K
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 of a...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
2.7K


