核剂和加工对聚乳酸结晶和机械性能的影响:一篇综述
Peng Gao1,2, Davide Masato1
1Department of Plastics Engineering, University of Massachusetts Lowell, Lowell, MA 18015, USA.
Micromachines
|June 27, 2024
概括
聚乳酸 (PLA) 是一种可生物降解的聚合物,其结晶速度缓慢,阻碍了其使用. 这篇评论详细介绍了配方,化合物和加工如何影响PLA结晶和机械性能,以获得更好的应用.
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
背景情况:
- 聚乳酸 (PLA) 是一种基于生物的,可生物降解的,无毒的聚合物,有可能取代基于石油的塑料.
- 它的半晶体性质为医疗植入物和药物输送系统等应用提供了希望.
- 然而,缓慢的结晶率阻碍了高效的制造,并限制了高度结晶的PLA产品的应用.
研究的目的:
- 审查和总结配方,复合和加工对PLA结晶行为的影响.
- 分析这些因素对关键结晶参数和机械性能的影响.
- 为 PLA 处理创新提供见解,以满足各种应用需求.
主要方法:
- 对研究PLA结晶和机械性能的文献综述.
- 分析影响结晶度,结晶率和结晶形态的因素.
- 评估机械性能,包括抗拉强度,模量,延长和抗冲击能力.
主要成果:
- 配方,复合和加工显著影响PLA的结晶率和结晶度.
- 结晶参数的变化与机械性能的变化直接相关,例如拉伸强度和抗冲击性.
- 可以优化特定的加工条件和添加剂配方,以提高PLA的晶体结构和性能.
结论:
- 了解配方,化合物,加工和PLA结晶之间的相互作用至关重要.
- 优化这些因素可以提高机械性能,并扩大PLA的应用潜力.
- 这种知识对于推进各种工业和生物医学用途的PLA加工技术至关重要.
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
Anionic Chain-Growth Polymerization: Overview
2.1K
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
2.1K
Ziegler–Natta Chain-Growth Polymerization: Overview
3.3K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.3K
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
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


