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相关概念视频

Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

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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.
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Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

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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 species into...
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Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

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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...
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Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

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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...
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Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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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...
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ATP and Macromolecule Synthesis01:28

ATP and Macromolecule Synthesis

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Biological macromolecules are organic compounds, predominantly composed of carbon atoms. The carbon atoms are covalently bonded with hydrogen, oxygen, nitrogen, and other minor elements. There are four major biological macromolecule classes: carbohydrates, lipids, proteins, and nucleic acids.
Most macromolecules are composed of single subunits, or building blocks, called monomers. The monomers combine with each other using covalent bonds to form larger molecules known as polymers.
Conversion of...
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通过原子转移合成的聚合物的电化学介导脱聚合 激进聚合.

Victoria Lohmann1, Lok Nga Poon2, Richard Whitfield1

  • 1Laboratory for Sustainable Polymers, Department of Materials, ETH Zürich, Vladimir-Prelog-Weg 5, 8093 Zürich, Switzerland.

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概括

电化学脱聚合提供了精确的控制聚合物回收,通过在活跃和休眠状态之间切换. 这种方法使用铁催化剂有效地从ATRP合成的聚合物中再生单体.

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科学领域:

  • 聚合物化学 聚合物化学
  • 电化学 电化学 电化学
  • 化学回收利用 化学回收利用

背景情况:

  • 聚合物的化学回收对于可持续性至关重要.
  • 传统的脱聚合方法在控制和效率方面存在局限性.
  • 原子转移激进聚合 (ATRP) 合成的聚合物存在独特的回收挑战.

研究的目的:

  • 引入电化学介导脱聚合 (EMD) 作为聚合物回收的新方法.
  • 用电化学开关来证明对脱聚合物的时间控制.
  • 将EMD与现有的脱聚合技术进行比较.

主要方法:

  • 使用铁催化剂去聚合ATRP合成的聚合物.
  • 应用电化学潜力来启动和调节脱聚合过程.
  • 在电化学,热,光学和化学脱聚合条件下比较单体回收率.

主要成果:

  • 使用EMD成功再生了高百分比的单体.
  • 在没有电化学输入的情况下发生了微不足道的脱聚合,使时间控制成为可能.
  • 在单体回收方面,EMD的性能优于热,光和化学方法.
  • 确定了新的溶剂,以促进低温脱聚合途径.

结论:

  • 电化学调解为聚合物脱聚合提供了有效的外部刺激.
  • 与传统方法相比,EMD提供了更高的控制和效率.
  • 这种方法显著扩大了化学回收技术的范围.