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Recrystallization: Solid–Solution Equilibria01:10

Recrystallization: Solid–Solution Equilibria

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Recrystallization is a purification technique used to separate impurities from solid compounds. In this technique, no chemical reactions occur. Instead, it exploits physical properties only, specifically, the solubility differences between the desired compound and impurities, either at a single temperature or at different temperatures, and under other selected conditions. The solid-solution equilibrium (solubility equilibrium) of each component in the solution represents a binary phase...
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Crystal Growth: Principles of Crystallization01:25

Crystal Growth: Principles of Crystallization

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Crystallization is a phase transformation process in which crystals are precipitated from a supersaturated solution or formed from other sources. During crystallization, atoms or molecules arrange themselves into a well-defined, rigid crystal lattice to minimize energy.
Initiating crystallization involves manipulating the concentration of the solute and the temperature of the solution. Since crystal growth occurs when the ratio of concentration and solubility of the solute in the solvent...
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Precipitation Processes01:12

Precipitation Processes

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The experimental conditions in a gravimetric analysis should be optimized to maximize the particle size and purity of the obtained precipitate. Ideally, the concentration of the precipitating reagent should be low with effective stirring to maintain low relative supersaturation for the growth of large crystals. In homogeneous precipitation, the precipitant is slowly generated by a chemical reaction in the solution to avoid local reagent excesses. For example, urea decomposes gradually to...
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Colloidal precipitates01:09

Colloidal precipitates

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The high insolubility of some precipitates can result in an unfavorable relative supersaturation. This can lead to colloidal particles with a large surface-to-mass ratio, where adsorption is promoted. For instance, in the precipitation of silver chloride, silver ions are adsorbed on the surface of the colloidal particles, forming a primary layer. This layer attracts ions of opposite charge (such as nitrate ions), forming a diffuse secondary layer of adsorbed ions. This electric double layer...
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Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism01:21

Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism

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Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
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Types of Coprecipitation01:10

Types of Coprecipitation

4.8K
Coprecipitation is the contamination of a precipitate by otherwise soluble species and occurs via different processes. In colloidal precipitates, coprecipitation occurs via surface adsorption. For instance, barium sulfate has a primary layer of adsorbed barium ions and a secondary layer of nitrate counterions. This results in contamination of the precipitate by barium nitrate.
Sometimes, ions in a crystal lattice can undergo isomorphous replacement by inclusions of similar charge and size. For...
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Heterogeneous Crystallization on Different Wetting Surfaces.

Tiantian Li1, Jianwen Zhang1, Jiashun Li1

  • 1State Key Laboratory for Environment-Friendly Energy Materials, School of Materials and Chemistry, Southwest University of Science and Technology, Mianyang 621010, PR China.

Langmuir : the ACS Journal of Surfaces and Colloids
|December 23, 2025
PubMed
Summary

Improving surface wetting enhances the nucleation barrier, inhibiting crystallization and scaling. Stable superhydrophobic surfaces, like micronano structures, significantly reduce calcium carbonate scaling for long-term anti-scaling applications.

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Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
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Area of Science:

  • Materials Science
  • Surface Chemistry
  • Nanotechnology

Background:

  • Scaling at solid-liquid interfaces poses challenges in industrial applications like pipeline transport and metal anticorrosion.
  • Understanding the relationship between surface wetting states and crystallization inhibition is crucial for developing effective anti-scaling solutions.

Purpose of the Study:

  • To investigate the scaling mechanism on surfaces with varying wetting states (flat, micron, nano, micronano).
  • To explore the potential of stable superhydrophobic surfaces for long-term anti-scaling applications.

Main Methods:

  • Fabrication of four representative surface structures: flat, micron, nano, and micronano.
  • Evaluation of heterogeneous nucleation barriers across different wetting states.
  • Assessment of calcium carbonate (CaCO3) scaling rates on various surfaces over 42 days and under dynamic conditions.

Main Results:

  • Enhanced wetting states positively influence the heterogeneous nucleation barrier, inhibiting crystallization.
  • Cassie-state superhydrophobic surfaces exhibit high nucleation barriers but can transition to Wenzel states, limiting long-term anti-scaling.
  • The micronano surface demonstrated superior stability, reducing CaCO3 scaling rate from 1.24 mg/cm2 to 0.335 mg/cm2 after 42 days.

Conclusions:

  • Achieving long-term anti-scaling requires stable Cassie-state superhydrophobicity.
  • Surface design strategies focusing on stable superhydrophobicity are essential for effective anti-scaling solutions in industrial settings.