脱聚变的热力学和动力学:什么使得乙烯基单体再生成为可能?
Victoria Lohmann1, Glen R Jones1, Nghia P Truong1,2
1Laboratory of Polymeric Materials, Department of Materials, ETH Zürich Vladimir-Prelog-Weg 5 8093 Zürich Switzerland athina.anastasaki@mat.ethz.ch.
Chemical science
|January 19, 2024
概括
激进脱聚合为塑料回收和循环聚合物经济提供了一个有前途的途径. 最近的进展表明,在较低的温度下几乎有数量的单体再生,彻底改变了塑料废物管理.
科学领域:
- 聚合物化学 聚合物化学
- 化学工程是化学工程的重要组成部分.
- 材料科学 材料科学 材料科学
背景情况:
- 塑料垃圾对环境构成重大挑战,阻碍了向循环经济过渡.
- 解聚合,一种将聚合物分解为单体的方法,对于具有全碳骨的聚合物来说是很困难的.
- 了解脱聚合的动力学和热力学对于开发有效的回收系统至关重要.
研究的目的:
- 探索激进脱聚合的热力学和动力学,用于添加聚合物.
- 将历史研究与该领域的最新进展联系起来.
- 突出催化方法在单体再生中的潜力.
主要方法:
- 审查20世纪中叶关于激进脱聚合的开创性研究.
- 对最近的研究进行分析,证明了低温,高产量的单体再生.
- 探索新兴的聚合物脱聚合的催化方法.
主要成果:
- 极端脱聚化可以实现近量化单体再生.
- 较低的反应温度是可行的,以实现有效的脱聚合.
- 催化方法对未来的应用有很大的前景.
结论:
- 对动力学和热力学的基本理解是推动脱聚合的关键.
- 最近的突破为塑料回收提供了一条革命性的道路.
- 催化脱聚合可能会将聚合物行业转变为可持续性.
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
Free-Radical Chain Reaction and Polymerization of Alkenes
7.8K
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.
7.8K
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
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
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
Anionic Chain-Growth Polymerization: Mechanism
2.0K
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
2.0K


