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相关概念视频

Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

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...
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

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 the...
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

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,...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

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 acceptor.
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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 generated carbocation,...
Accelerated Curing of Concrete01:25

Accelerated Curing of Concrete

Accelerating concrete curing is achieved by applying heat and additional moisture. This process accelerates the hydration of the cement, resulting in an earlier strength gain in the concrete. Steam curing is a method wherein the concrete products are either transported through a chamber on a conveyor belt or encased in plastic, allowing steam at atmospheric pressure to circulate freely around them. This process begins with a phase of moist curing that typically lasts between 3 to 5 hours, after...

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相关实验视频

Updated: Jul 9, 2026

Aqueous Droplets Used as Enzymatic Microreactors and Their Electromagnetic Actuation
08:27

Aqueous Droplets Used as Enzymatic Microreactors and Their Electromagnetic Actuation

Published on: August 28, 2017

聚合物刷的快速生长来自固定启动器.

Zhiyi Bao1, Merlin L Bruening, Gregory L Baker

  • 1Department of Chemistry, Michigan State University, East Lansing, Michigan 48824, USA.

Journal of the American Chemical Society
|July 13, 2006
PubMed
概括
此摘要是机器生成的。

研究人员开发了一种快速的方法来合成聚合物刷,使用50°C的表面启动聚合. 这种新技术显著加速了聚合物刷子的生长,为传统方法提供了更快的替代方案.

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Creating Rapid Oxygen Oscillations in Microbial Single-cell Growth Analysis using a Microfluidic Double-layer Device
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科学领域:

  • 聚合物化学 聚合物化学
  • 材料科学 材料科学 材料科学
  • 表面科学是一门学科.

背景情况:

  • 表面启动的聚合对于创建功能性材料至关重要.
  • 传统方法往往受到反应速度缓慢和控制有限的影响.
  • 开发快速和可控的聚合技术对于先进的应用是必不可少的.

研究的目的:

  • 报告一种用于快速聚合物刷合成的新,高效的方法.
  • 为了证明该方法与不同单体的多功能性.
  • 为了比较实现的增长率与传统的聚合技术.

主要方法:

  • 在温和条件下 (50°C) 利用表面启动的原子转移基聚合 (ATRP).
  • 采用一种高度活性的基于铜的催化剂 (Cu) -1,4,8,11-四甲基-1,4,8,11-四环氧三甲基).
  • 从启动器修改的黄金表面开始的聚合.

主要成果:

  • 在短短5分钟内完成了100纳米厚的聚乙烯酸三烯酸) 刷的合成.
  • 在10分钟和60分钟内分别制造出100纳米厚的2-乙基甲酸盐和甲基甲酸盐薄膜.
  • 证明的聚合率比传统的自由基聚合速度快一级.

结论:

  • 开发的方法使得在温和条件下显著快速的聚合物刷合成.
  • 该技术保留了受控激素聚合的特征,包括块共聚合物形成.
  • 这一进步为表面启动的聚合物效率提供了显著的改进.