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相关概念视频

Precipitate Formation and Particle Size Control01:16

Precipitate Formation and Particle Size Control

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In precipitation gravimetry, the precipitating agent should react specifically or selectively with the analyte. While a specific reagent reacts with the analyte alone, a selective reagent can react with a limited number of chemical species.
The obtained precipitate should be either a pure substance of known composition or easily converted to one by a simple process, such as ignition or drying. In addition, the precipitate should be insoluble and easily filterable. In general, filterability...
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Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model01:09

Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model

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Various dissolution theories provide insight into the factors that influence the dissolution rate. Danckwerts' Model suggests that turbulence, rather than a stagnant layer, characterizes the dissolution medium at the solid-liquid interface. In this model, the agitated solvent contains macroscopic packets that move to the interface via eddy currents, facilitating the absorption and delivery of the drug to the bulk solution. The regular replenishment of solvent packets maintains the...
764
Factors Affecting Dissolution: Particle Size and Effective Surface Area01:23

Factors Affecting Dissolution: Particle Size and Effective Surface Area

1.6K
Dissolution kinetics, an essential aspect of oral drug delivery, is significantly influenced by the drug's particle size. According to the Noyes-Whitney dissolution model, the dissolution rate correlates directly with the drug's surface area. The larger the surface area, the higher the drug's solubility in water, leading to a faster drug dissolution rate. Reducing particle size increases the effective surface area, enhancing the dissolution process. Micronization and nanosizing are...
1.6K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

4.3K
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...
4.3K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

3.4K
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...
3.4K
Factors Affecting Activity Coefficient01:17

Factors Affecting Activity Coefficient

1.5K
The extended Debye-Hückel equation indicates that the activity coefficient of an ion in an aqueous solution at 25°C depends on three partially interdependent properties: the ionic strength of the solution, the charge of the ion, and the ion size. 
The activity coefficient value for an ion is close to one when the solution has almost zero ionic strength, i.e., when the solution shows close to ideal behavior. As the ionic strength of the solution increases from 0 to 0.1 mol/L, a...
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相关实验视频

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An Analog Macroscopic Technique for Studying Molecular Hydrodynamic Processes in Dense Gases and Liquids
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活性模型B+中的化动力学:宏观和微观阶段分离.

Pradeep Kumar Yadav1, Shradha Mishra2, Sanjay Puri1

  • 1Jawaharlal Nehru University, School of Physical Sciences, New Delhi 110067, India.

Physical review. E
|October 21, 2025
PubMed
概括

活跃模型B+中的活跃布朗粒子由于宏观阶段分离期间的循环质量转移,表现出较慢的粗化动态. 微尺度相位分离的结果是单分散滴的稳定状态晶体.

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:

  • 活跃的布朗粒子 (ABP) 对于理解自动驱动物质至关重要.
  • 活跃模型B+ (AMB+) 将B模型概括为保留顺序参数,并结合了活动术语.
  • 活性物质系统中的相位分离对于自我组织至关重要.

研究的目的:

  • 通过使用Active Model B+数量研究活跃布朗粒子的粗化动力学.
  • 在AMB+中分析宏观阶段分离 (MPS) 和微观阶段分离 (μPS).
  • 阐明活动项 (λ 和 ξ) 在相隔动态上的作用.

主要方法:

  • 积极模型B+的全面数值模拟.
  • 在临界构成和旋分解下分析粗化动力学.
  • 顺序参数电流模式和质量转移机制的表征.

主要成果:

  • 在MPS期间,AMB+表现出较慢的域增长 (指数1/4) 由于滴滴之间的循环质量转移.
  • 在MPS中,沿域壁观察到一个不同的交替电流循环和节点模式.
  • 对于其他参数范围,AMB+显示μPS,形成单分散滴的晶体.

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结论:

  • 与被动系统相比,AMB+中独特的电流结构显著影响了粗化动力学.
  • AMB+显示了丰富的相隔行为,包括缓慢粗的MPS和有序结构的μPS.
  • 这项研究提供了对主动物质自我组织和模式形成的基本物理学的见解.