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Gravimetry: Inorganic And Organic Precipitating Agents00:49

Gravimetry: Inorganic And Organic Precipitating Agents

1.2K
In gravimetry, the precipitant is chosen carefully to obtain a pure solid that can be easily filtered. Common inorganic precipitants can be used to determine several cations and anions. In some cases, the formation of the same precipitate can be used to determine the cation and the anion. For example, the reaction of barium and chromate ions to give barium chromate is used to determine both barium and chromate. However, precipitates such as hydroxides, oxalates, and metal ammonium phosphates...
1.2K
Types of Coprecipitation01:10

Types of Coprecipitation

569
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...
569
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

460
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
460
Colloidal precipitates01:09

Colloidal precipitates

515
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...
515
Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

2.8K
Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
2.8K
Complexometric Titration: Ligands00:43

Complexometric Titration: Ligands

912
Different monodentate and polydentate ligands are used as complexing agents in complexometric titration reactions. The formation of complexes by mono- and bidentate ligands involves two or more intermediate steps, limiting their use as complexing agents. In comparison, polydentate ligands can form complexes with metal ions in a single-step process, facilitating sharper end points. This means polydentate ligands, such as amino carboxylic acid derivatives, are most commonly employed in...
912

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Related Experiment Video

Updated: Jun 6, 2025

Fabrication Procedures and Birefringence Measurements for Designing Magnetically Responsive Lanthanide Ion Chelating Phospholipid Assemblies
09:38

Fabrication Procedures and Birefringence Measurements for Designing Magnetically Responsive Lanthanide Ion Chelating Phospholipid Assemblies

Published on: January 3, 2018

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Structure-Function Insights into Thermoresponsive Copolymers as Lanthanide Precipitants.

Supraja S Chittari1, Peter A Dykeman-Bermingham1, Matthew P Bogen1

  • 1Department of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.

Journal of the American Chemical Society
|November 25, 2024
PubMed
Summary

This study details how copolymer composition influences lanthanide ion separation. Increased hydrophobicity enhances extraction efficiency, revealing a binding-then-assembly mechanism for metal ion coprecipitation.

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Synthesis of Core-shell Lanthanide-doped Upconversion Nanocrystals for Cellular Applications
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Preparation, Purification, and Characterization of Lanthanide Complexes for Use as Contrast Agents for Magnetic Resonance Imaging
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Preparation, Purification, and Characterization of Lanthanide Complexes for Use as Contrast Agents for Magnetic Resonance Imaging
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Preparation, Purification, and Characterization of Lanthanide Complexes for Use as Contrast Agents for Magnetic Resonance Imaging

Published on: July 21, 2011

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Area of Science:

  • Polymer Chemistry
  • Materials Science
  • Separation Science

Background:

  • Stimuli-responsive polymers offer tunable properties for diverse applications.
  • Designing synthetic polymers requires understanding composition-structure-function relationships.
  • Lanthanide ion separation is critical for various technologies.

Purpose of the Study:

  • To systematically investigate the relationship between copolymer composition, structure, and function in lanthanide ion extraction.
  • To elucidate the mechanism of lanthanide ion isolation using stimuli-responsive copolymers.
  • To optimize copolymer design for efficient and selective metal ion separation.

Main Methods:

  • Synthesis of copolymers with thermoresponsive (N-isopropylacrylamide), metal-chelating (acrylic acid), and hydrophobic comonomers.
  • Quantification of lanthanide ion extraction efficiency using a metallochromic dye.
  • Analysis of polymer solution-phase conformation via techniques sensitive to hydrophobic interactions.
  • Correlation of comonomer structure and sequence with extraction performance.

Main Results:

  • Copolymer hydrophobicity directly correlates with improved lanthanide ion separation efficiency.
  • Specific hydrophobic comonomer features significantly influence polymer conformation and metal binding.
  • Multiblock polymerization enhances metal extraction by controlling subunit proximity.
  • A binding-then-assembly mechanism is proposed for metal ion coprecipitation.

Conclusions:

  • Copolymer design, particularly hydrophobicity and subunit arrangement, is key to efficient lanthanide ion extraction.
  • Understanding polymer conformation in solution is crucial for optimizing separation processes.
  • The proposed binding-then-assembly mechanism provides a framework for designing advanced chelating polymers.