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Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

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Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
2.2K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.4K
Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
3.4K
Passive Diffusion: Overview and Kinetics01:17

Passive Diffusion: Overview and Kinetics

425
Passive diffusion is a critical process that allows small lipophilic drugs to cross the cell membrane along a concentration gradient. This mechanism's efficiency depends on four primary factors: the membrane's surface area, the drug's lipid-water partition coefficient, the concentration gradient, and the membrane's thickness.
When administered orally, drugs establish a substantial concentration gradient between the gastrointestinal (GI) lumen and the bloodstream, expediting...
425
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
Predicting Reaction Outcomes02:24

Predicting Reaction Outcomes

8.2K
Kinetics describes the rate and path by which a reaction occurs. In contrast, thermodynamics deals with state functions and describes the properties, behavior, and components of a system. It is not concerned with the path taken by the process and cannot address the rate at which a reaction occurs. Although it does provide information about what can happen during a reaction process, it does not describe the detailed steps of what appears on an atomic or a molecular level. On the other hand,...
8.2K

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Updated: Jun 11, 2025

Saccharomyces cerevisiae Exponential Growth Kinetics in Batch Culture to Analyze Respiratory and Fermentative Metabolism
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Saccharomyces cerevisiae Exponential Growth Kinetics in Batch Culture to Analyze Respiratory and Fermentative Metabolism

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在活性二元混合物中的域增长动力学.

Sayantan Mondal1, Prasenjit Das1

  • 1Department of Physical Sciences, Indian Institute of Science Education and Research Mohali, Knowledge City, Sector 81, SAS Nagar, Mohali, Punjab 140306, India.

The Journal of chemical physics
|October 1, 2024
PubMed
概括
此摘要是机器生成的。

本研究探讨了活性混合物中运动性诱导的相分离. 域大小以扩散方式增长 (L(t) ~ t1/3),其缩放功能取决于组成和相对物种活动.

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科学领域:

  • 物理 物理学 物理
  • 软物质物理学 软物质物理学
  • 统计力学 统计力学

背景情况:

  • 活性物质系统表现出在平衡系统中看不到的独特的集体行为.
  • 运动诱导相分离 (MIPS) 是活性物质中的一个关键现象,导致自我组织.
  • 了解混合物中的MIPS对于设计活性材料至关重要.

研究的目的:

  • 在对称和不对称的活性二元混合物中研究相位分离动力学.
  • 描述MIPS期间域的形态和缩放行为.
  • 为了确定混合物成分和相对物种活动对相位分离的影响.

主要方法:

  • 利用粗的跑动细菌模型来推导密度场进化方程.
  • 在解决进化方程和模拟相位分离动态方面采用欧勒离散式.
  • 通过使用等时相关函数 (C,r,t) 和结构因子 (S,k,t) 来分析域形态.

主要成果:

  • 观察到C{r,t) 和S{k,t) 的动态缩放,表明自相似的域增长.
  • 证明缩放函数形式取决于混合物组成和相对活性 (Δ).
  • 在所有混合物的大波向量中确认了扩散域增长 (L{t) ~ t1/3) 和波罗德定律 (S{k,t) ~ k-{d+1)).

结论:

  • 活跃的二进制混合物表现出MIPS,具有普遍的扩散生长和缩放行为.
  • 混合物成分和相对活性是控制MIPS形态的关键参数.
  • 这些发现提供了对主动复杂流体自我组织的基本原则的洞察.