化学可回收的乙烯基聚合物通过循环烯衍生物的自由基聚合
Yota Chiba1, Ryo Kawatani1, Yasuhiro Kohsaka1,2
1Faculty of Textile Science and Technology, Shinshu University, 3-15-1 Tokida, Ueda, Nagano 386-8567, Japan.
ACS macro letters
|November 27, 2023
概括
现在可以使用化学回收维尼尔聚合物 (VPs). 修改循环烯衍生物增强了固态阻碍,促进了主链裂变和脱聚合,以恢复单体,有助于资源循环.
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
- 化学回收利用 化学回收利用
背景情况:
- 实现一个可持续的社会需要有效的资源循环.
- 乙烯基聚合物 (VPs) 由于选择性脱聚合的困难,难以化学回收.
- 新的VP回收方法对于可持续的材料管理至关重要.
研究的目的:
- 研究由循环 styrene 衍生物制成的乙烯聚合物的化学可回收性.
- 开发一种高效的方法来使VPs脱聚化为它们的组成单体.
- 为实现可持续的未来,为资源循环战略做出贡献.
主要方法:
- 来自循环 styrene 衍生物的乙烯基聚合物的合成和表征.
- 通过悬挂组修改 (肥化) 调查聚合物主链裂变.
- 使用水性氧化物 (KOH) 优化脱聚合条件.
主要成果:
- 在循环 styrene 衍生物 VPs 中,悬挂组的肥化增加了固体阻碍.
- 增加的固体障碍促进了选择性主链裂变和脱聚合.
- 通过将聚合物悬浮在水性KOH中来实现VP的高效化学回收.
结论:
- 开发的方法使特定的乙烯基聚合物能够有效地进行化学回收.
- 这种方法促进了乙烯基单体的回收,支持循环经济.
- 这些发现为聚合物行业的可持续资源管理提供了一条途径.
相关概念视频
Radical Chain-Growth Polymerization: Mechanism
2.6K
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...
2.6K
Free-Radical Chain Reaction and Polymerization of Alkenes
7.9K
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.
7.9K
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
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
Radical Chain-Growth Polymerization: Chain Branching
1.9K
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
1.9K
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


