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Related Concept Videos

Solid–Solid Solutions01:24

Solid–Solid Solutions

The temperature-composition phase diagram of two solids, A and B, which are immiscible in the solid phase but form miscible liquids, shows that when the temperature is low, these two exist as separate, pure solids (A and B). As the temperature increases, they transition into a single-phase liquid solution where A and B coexist. Moving from point a1 to a2 in the phase diagram, the composition changes such that solid B begins to separate from the solution, enriching the remaining liquid with A.
Recrystallization: Solid–Solution Equilibria01:10

Recrystallization: Solid–Solution Equilibria

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...
Precipitation Processes01:12

Precipitation Processes

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...
Types of Coprecipitation01:10

Types of Coprecipitation

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...
Colloidal precipitates01:09

Colloidal precipitates

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...
Phase Transitions: Vaporization and Condensation02:39

Phase Transitions: Vaporization and Condensation

The physical form of a substance changes on changing its temperature. For example, raising the temperature of a liquid causes the liquid to vaporize (convert into vapor). The process is called vaporization—a surface phenomenon. Vaporization occurs when the thermal motion of the molecules overcome the intermolecular forces, and the molecules (at the surface) escape into the gaseous state. When a liquid vaporizes in a closed container, gas molecules cannot escape. As these gas phase molecules...

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Fabricating High-viscosity Droplets using Microfluidic Capillary Device with Phase-inversion Co-flow Structure
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Spinodal decomposition and droplets entrapment in monotectic solidification.

F Wang1, A Choudhury, C Strassacker

  • 1Institute of Materials and Processes, Karlsruhe University of Applied Sciences, Moltkestrasse 30, 76133 Karlsruhe, Germany.

The Journal of Chemical Physics
|July 27, 2012
PubMed
Summary

This study introduces two models for simulating solidification in monotectic alloys. The second model successfully simulates larger scales, revealing how surface energy and undercooling impact dynamic entrapment during monotectic reactions.

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Area of Science:

  • Materials Science
  • Computational Materials Science

Background:

  • Monotectic alloys exhibit complex solidification morphologies.
  • Simulating these morphologies requires accurate models that can handle phase separation and interfacial phenomena.

Purpose of the Study:

  • To present two distinct phase-field models for simulating solidification morphologies in monotectic alloys.
  • To investigate morphological evolution influenced by spinodal decomposition using a nanometer-scale model.
  • To develop and apply a second model for simulating larger scales, focusing on the dynamic entrapment process in monotectic reactions.

Main Methods:

  • The first model incorporates a gradient energy contribution to stabilize phase separation within the miscibility gap, using bulk energy density interpolation.
  • The second model excludes concentration gradient contributions for larger-scale simulations, adapting existing phase-field approaches.
  • The second model was employed to simulate the dynamic entrapment process, analyzing the effects of liquid-liquid surface energy and undercooling.

Main Results:

  • The first model is limited to nanometer scales due to surface excess contributions.
  • The second model allows for larger-scale simulations with higher interface widths by eliminating equilibrium free energy excess across the interface.
  • Simulations using the second model demonstrated the influence of liquid(1)-liquid(2) surface energy and undercooling on the dynamic entrapment process.

Conclusions:

  • Two phase-field models were developed for monotectic alloy solidification.
  • The second model offers advantages for larger-scale simulations and studying dynamic processes like entrapment.
  • Surface energy and undercooling are critical parameters influencing dynamic entrapment in monotectic reactions.