Jove
Visualize
Contact Us

Related Concept Videos

Complexation Equilibria: Overview01:23

Complexation Equilibria: Overview

752
Complexation reactions take place when dative or coordinate covalent bonds form between metal ions and ligands. The compounds formed in these reactions are called coordination compounds. The number of bonds formed between the metal ion and the ligands is called its coordination number. Generally, most metal ions in an aqueous solution are solvated by water molecules and thus exist as aqua complexes.
The equilibrium constant of the complexation reaction is represented as the formation constant...
752
Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

26.9K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
26.9K
Susceptibility, Permittivity and Dielectric Constant01:26

Susceptibility, Permittivity and Dielectric Constant

1.7K
When placed in an external electric field, a dielectric material gets polarized. The charge density in the dielectric material is given by the sum of the bound and free charge densities, while the total charge density can also be written in terms of the total electric field. The bound charge density can be measured in terms of polarization, leading to the relationship between electric displacement and polarization.
1.7K
Factors Affecting Activity Coefficient01:17

Factors Affecting Activity Coefficient

841
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...
841
Solubility Equilibria: Overview01:09

Solubility Equilibria: Overview

729
When a substance such as sodium chloride is added to water, it dissolves, forming an aqueous solution. The extent of dissolution is called solubility. The process of dissolution can exist in equilibrium, just like other chemical processes. Solubility equilibria are also called precipitation equilibria because the process of solubility can be reversible. The reverse of the solubility process is called precipitation.
Solubility is important in biological and environmental processes. A notable...
729
EDTA: Conditional Formation Constant01:09

EDTA: Conditional Formation Constant

986
Each EDTA molecule has six binding sites: four carboxyl groups and two amino groups. The fully protonated form of EDTA is represented as H6Y2+. However, it can exist in different forms, H5Y+, H4Y, H3Y−, H2Y2−, and HY3−, depending on the pH of the solution. In very basic solutions with pH > 10.17, the fully deprotonated form, Y4−, is the predominant species that readily complexes with metal ions in a 1:1 ratio.
For the equilibrium reaction of the metal with the...
986

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Fortification of Wheat Bread with Increasing Levels of Kudzu (<i>Pueraria lobata</i>) Root Powder: Technological, Nutritional, and Sensory Implications.

Foods (Basel, Switzerland)·2026
Same author

Pyrite (001) Interface Chemistry is Controlled by a Sulfoxy Termination.

Langmuir : the ACS journal of surfaces and colloids·2026
Same author

What Really Matters in Weight Loss after Bariatric Surgery - 10 Years Follow-Up (BARI-10 -POL Study).

Obesity surgery·2025
Same author

Defect-Mediated Diffusion Pathways in Spodumene Accelerate Lithium Transport.

ACS materials letters·2025
Same author

Multistage nucleation pathway in LiF molten salt mirrors the crystal-melt interface structure.

Proceedings of the National Academy of Sciences of the United States of America·2025
Same author

pH-dependent reactivity of water at MgO(100) and MgO(111) surfaces.

Physical chemistry chemical physics : PCCP·2025
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Video

Updated: Jul 30, 2025

Expression of Cementitious Pore Solution and the Analysis of Its Chemical Composition and Resistivity Using X-ray Fluorescence
06:27

Expression of Cementitious Pore Solution and the Analysis of Its Chemical Composition and Resistivity Using X-ray Fluorescence

Published on: September 23, 2018

9.4K

Distance-dependent dielectric constant at the calcite/electrolyte interface: Implication for surface complexation

Piotr Zarzycki1

  • 1Energy Geosciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA, United States.

Journal of Colloid and Interface Science
|May 12, 2023
PubMed
Summary

Molecular simulations reveal oscillating dielectric constants at mineral interfaces, challenging continuum models. This study links water density to dielectric properties, enabling accurate estimation of capacitances for mineral/electrolyte systems.

Keywords:
Calcite/electrolyte interfaceCapacitanceElectric double layerIce-like waterInterfacial dielectric constantMolecular dynamics

More Related Videos

Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid
08:54

Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid

Published on: January 25, 2020

5.7K
Microfluidic Device for the Separation of Non-Metastatic MCF-7 and Non-Tumor MCF-10A Breast Cancer Cells Using AC Dielectrophoresis
08:33

Microfluidic Device for the Separation of Non-Metastatic MCF-7 and Non-Tumor MCF-10A Breast Cancer Cells Using AC Dielectrophoresis

Published on: August 11, 2022

2.5K

Related Experiment Videos

Last Updated: Jul 30, 2025

Expression of Cementitious Pore Solution and the Analysis of Its Chemical Composition and Resistivity Using X-ray Fluorescence
06:27

Expression of Cementitious Pore Solution and the Analysis of Its Chemical Composition and Resistivity Using X-ray Fluorescence

Published on: September 23, 2018

9.4K
Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid
08:54

Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid

Published on: January 25, 2020

5.7K
Microfluidic Device for the Separation of Non-Metastatic MCF-7 and Non-Tumor MCF-10A Breast Cancer Cells Using AC Dielectrophoresis
08:33

Microfluidic Device for the Separation of Non-Metastatic MCF-7 and Non-Tumor MCF-10A Breast Cancer Cells Using AC Dielectrophoresis

Published on: August 11, 2022

2.5K

Area of Science:

  • Physical Chemistry
  • Computational Materials Science
  • Surface Science

Background:

  • The electrical double layer at mineral/electrolyte interfaces is typically modeled using continuum approaches assuming a monotonic decrease in solvent dielectric constant near the surface.
  • Molecular simulations reveal oscillatory solvent polarizability and density profiles, contradicting the monotonic assumption.
  • Reconciling molecular and mesoscale descriptions is crucial for accurate interfacial modeling.

Purpose of the Study:

  • To investigate the relationship between interfacial water density and the dielectric constant.
  • To develop a computationally efficient method for determining dielectric properties of interfacial water.
  • To estimate capacitances for Surface Complexation Models (SCMs) using molecularly informed dielectric properties.

Main Methods:

  • Molecular dynamics simulations of the calcite 101¯4/electrolyte interface.
  • Calculation of distance-dependent static dielectric constant and water density profiles.
  • Spatial averaging of dielectric constants and application of a parallel-plate capacitor model for SCM capacitance estimation.

Main Results:

  • Confirmed strong correlation between dielectric constant oscillations and water density profiles at the interface.
  • Developed a linear regression model to estimate dielectric constant from water density, significantly reducing computational cost.
  • Observed that electrolyte ions decrease interfacial dielectric constant by reducing water density and altering water dipole orientation.

Conclusions:

  • Spatially averaging molecularly derived dielectric constants reconciles molecular and mesoscale models of the electrical double layer.
  • Water density serves as a reliable predictor for interfacial dielectric properties, offering a computational shortcut.
  • This approach enables accurate estimation of SCM capacitances using molecularly informed dielectric constants and hydration layer positions.