在PLA分解和PTMC形成中的协同途径:一个单一的Eutectic驱动的回收机制
Sébastien Moins1, Olivier Coulembier1
1Laboratory of Polymeric and Composite Materials, University of Mons, Place du Parc 23, 7000, Mons-, Belgium.
Angewandte Chemie (International ed. in English)
|December 23, 2024
概括
本研究提出了一种单一的方法,通过脱聚化和同时聚合三甲基碳酸盐 (TMC) 来化学回收聚乳酸 (PLA). 这种高效的工艺可以产生可调节的聚三甲碳酸 (PTMC),而无需干燥材料.
科学领域:
- 聚合物化学 聚合物化学
- 可持续材料科学科学 可持续材料科学
- 化学工程是化学工程的重要组成部分.
背景情况:
- 聚乳酸 (PLA) 是一种广泛使用的可生物降解聚合物,但其有效的化学回收仍然是一个挑战.
- 在循环经济倡议中,开发用于PLA价值化的可持续方法至关重要.
- 现有的方法通常需要恶劣的条件或多个步骤,限制了它们的工业适用性.
研究的目的:
- 开发一种新的,高效的单战略,用于化学价值化聚乳酸 (PLA).
- 将PLA的基催化脱聚合与三甲烯碳酸盐 (TMC) 的环开聚合 (ROP) 结合起来.
- 从PLA废物中生产有价值的聚三甲碳酸 (PTMC).
主要方法:
- 使用乳化物 (LA) 和三甲基碳酸盐 (TMC) 的欧混合物来降低PLA降解所需的热输入.
- 使用双功能的氧化 (KOArtBu) 催化剂来调节PLA脱聚合和TMC聚合.
- 在剩余水的存在下进行反应,消除了严格干燥程序的需要.
主要成果:
- 实现了PLA的选择性化学分解转化.
- 成功生产了 (oligo) 乳酸末盖聚二甲基碳酸 (PTMC).
- 通过控制含水量来证明得到的PTMC的可调节的质量.
结论:
- 开发的一策略为PLA化学回收提供了一个高效和实用的途径.
- 该过程绕过了大量干燥的需要,简化了整体程序.
- 这种方法提供了一种可持续的途径,可以将PLA废物再循环转化为具有可控性质的有价值的PTMC材料.
相关概念视频
Radical Chain-Growth Polymerization: Mechanism
2.5K
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this...
2.5K
Olefin Metathesis Polymerization: Overview
2.0K
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...
2.0K
Free-Radical Chain Reaction and Polymerization of Alkenes
7.7K
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.
7.7K
Radical Chain-Growth Polymerization: Overview
2.4K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
2.4K
Thermal and Photochemical Electrocyclic Reactions: Overview
2.3K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
2.3K
Cationic Chain-Growth Polymerization: Mechanism
2.2K
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
2.2K


