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相关概念视频

Radical Chain-Growth Polymerization: Chain Branching01:17

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
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.3K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.3K
Entropy Change in Reversible Processes01:10

Entropy Change in Reversible Processes

2.5K
In the Carnot engine, which achieves the maximum efficiency between two reservoirs of fixed temperatures, the total change in entropy is zero. The observation can be generalized by considering any reversible cyclic process consisting of many Carnot cycles. Thus, it can be stated that the total entropy change of any ideal reversible cycle is zero.
The statement can be further generalized to prove that entropy is a state function. Take a cyclic process between any two points on a p-V diagram.
2.5K
Radical Chain-Growth Polymerization: Mechanism01:09

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
Radical Chain-Growth Polymerization: Overview01:10

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
Entropy and Solvation02:05

Entropy and Solvation

7.0K
The process of surrounding a solute with solvent is called solvation. It involves evenly distributing the solute within the solvent. The rule of thumb for determining a solvent for a given compound is that like dissolves like. A good solvent has molecular characteristics similar to those of the compound to be dissolved. For example, polar solutions dissolve polar solutes, and apolar solvents dissolve apolar solutes. A polar solvent is a solvent that has a high dielectric constant (ϵ...
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相关实验视频

Updated: Jun 28, 2025

An Analog Macroscopic Technique for Studying Molecular Hydrodynamic Processes in Dense Gases and Liquids
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An Analog Macroscopic Technique for Studying Molecular Hydrodynamic Processes in Dense Gases and Liquids

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在相互作用的可整合链中,挤压组合和异常的动态化.

Guillaume Cecile1, Jacopo De Nardis1, Enej Ilievski2

  • 1Laboratoire de Physique Théorique et Modélisation, CNRS UMR 8089, CY Cergy Paris Université, 95302 Cergy-Pontoise Cedex, France.

Physical review letters
|April 13, 2024
PubMed
概括

某些量子系统避免了典型的热化,放松到具有不寻常波动的异国情境. 这项研究在可整合的量子模型中探索了这些异常行为,为冷原子实验提供了可测试的预测.

科学领域:

  • 凝聚物质物理学 凝聚物质物理学
  • 量子多体系统是一个量子多体系统.
  • 统计力学 统计力学

背景情况:

  • 预计孤立的可整合量子系统将与一般化的吉布斯集合保持平衡.
  • 规范性热化描述了在这样的系统中预期的放松动态.

研究的目的:

  • 识别和描述与标准通用热化偏离的相互作用可整合模型中的初始状态.
  • 研究异常量子运输和特定量子状态的波动.

主要方法:

  • 在轻轴模式下分析量子XXZ链.
  • 对缺乏磁波动的纯非平衡初始状态的研究.
  • 检查放松动态和波动特性.

主要成果:

  • 非波动的初始状态放松到压缩的一般化吉布斯合奏,带有低级电荷波动.
  • 在同otropic 点,从 Néel 状态的放松表现出广泛的波动和超扩散缩放 (Kardar-Parisi-Zhang 通用性).
  • 其他非波动状态,如旋单子,显示扩散缩放.

结论:

  • 在可整合模型中展示了一类避开正规热化的初始状态.

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  • 突出异国情调的平衡状态,具有异常的缩放和波动.
  • 提供关于量子运输的冷原子系统的实验可测试预测.