Jove
Visualize
Contact Us
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 Concept Videos

Ion Exchange01:17

Ion Exchange

Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or basic...
Electrolyte and Nonelectrolyte Solutions02:21

Electrolyte and Nonelectrolyte Solutions

Substances that undergo either a physical or a chemical change in solution to yield ions that can conduct electricity are called electrolytes. If a substance yields ions in solution, that is, if the compound undergoes 100% dissociation, then the substance is a strong electrolyte. Complete dissociation is indicated by a single forward arrow. For example, water-soluble ionic compounds like sodium chloride dissociate into sodium cations and chloride anions in aqueous solution.
Aqueous Solutions and Heats of Hydration02:42

Aqueous Solutions and Heats of Hydration

Water and other polar molecules are attracted to ions. The electrostatic attraction between an ion and a molecule with a dipole is called an ion-dipole attraction. These attractions play an important role in the dissolution of ionic compounds in water.
When ionic compounds dissolve in water, the ions in the solid separate and disperse uniformly throughout the solution because water molecules surround and solvate the ions, reducing the strong electrostatic forces between them. This process...
Titration in Nonaqueous Solvents01:16

Titration in Nonaqueous Solvents

Most acid-base titrations are performed in an aqueous medium. In aqueous titrations, water competes with weaker acids or bases for proton donation or acceptance, leading to ambiguous endpoints in the titration curve. Water also affects the partial ionization of weak acids or bases. For example, water accepts a proton from acetic acid to form hydronium and acetate ions. The hydronium ion formed is a stronger acid than acetic acid, and the acetate ion is a stronger base than water. As a result,...
Solubility Equilibria: Ionic Product of Water01:16

Solubility Equilibria: Ionic Product of Water

Pure water is a weak electrolyte; only a small amount ionizes into hydrogen and hydroxide ions. At any given temperature, the concentration of undissociated water is almost constant, so the ionic product of water is the product of the hydrogen and hydroxide ion concentrations, denoted as Kw. The square root of Kw gives the individual ion concentrations.
The ionic product of water varies with temperature, and its value is 1.0 x 10−14 at standard experimental conditions. Per Le Chatelier's...
Ionic Strength: Overview01:12

Ionic Strength: Overview

The ionic strength of a solution is a quantitative way of expressing the total electrolyte concentration of a solution. This concept was first introduced in 1921 by two American physical chemists, Gilbert N. Lewis and Merle Randall, while describing the activity coefficient of strong electrolytes. During the calculation of ionic strength (I or μ), all the cations and anions are considered. However, the concentration (c) of an ion with a greater charge number (z) has a greater contribution to...

You might also read

Related Articles

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

Sort by
Same author

Synthesis of lignin nanoparticles using CO<sub>2</sub>-responsive amines and their performance as UV-light shields.

RSC advances·2026
Same author

Forward osmosis followed by reverse osmosis for the removal of contaminants of emerging concern using a CO<sub>2</sub>-responsive draw agent.

Journal of hazardous materials·2025
Same author

Mechanochemical and Aging-Based S<sub>N</sub>2 Method to Access CO<sub>2</sub>-Responsive, High-Amine-Loading Chitosan.

ChemSusChem·2025
Same author

Simultaneous switching of two different CO<sub>2</sub>-switchable amines in the same solution.

Physical chemistry chemical physics : PCCP·2024
Same author

CO<sub>2</sub>-Responsive Low Molecular Weight Polymer with High Osmotic Pressure as a Draw Solute for Forward Osmosis.

ACS omega·2024
Same author

CO<sub>2</sub>-Switchable colloids.

Chemical communications (Cambridge, England)·2023
Same journal

Interface Engineering: Heterogeneous Nickel-Iron Sulfide Decorated Nitrogen-Doped-Graphene for Efficient Water Splitting.

ChemSusChem·2026
Same journal

Potassium-Ion Pillared Basic Copper Molybdate Nanoflowers as High-Performance Cathodes for Stable Aqueous Ammonium-Ion Batteries.

ChemSusChem·2026
Same journal

Phosphate-Terminated Nb<sub>2</sub>C MXene as Efficient Catalyst for the Transformation of Glucose Into 5-Hydroxymethylfurfural With 3077 h<sup>-1</sup> Turnover Frequency.

ChemSusChem·2026
Same journal

Efficient Polyethylene Furanoate Synthesis From CO<sub>2</sub> and 5-(Hydroxymethyl)furfural.

ChemSusChem·2026
Same journal

La<sub>0.7</sub>Sr<sub>0.3</sub>Al<sub>0.7</sub>Ti<sub>0.3</sub>O<sub>3-δ</sub> Dual-Conductor Anode in SOFC for Co-Generation of Olefin and Electricity.

ChemSusChem·2026
Same journal

Mitigating Dissolution and Kinetics Limitations in Aqueous Zinc-Organic Batteries via a Conjugated Scaffold Integrated With Stable Nitroxyl Radicals.

ChemSusChem·2026
See all related articles

Related Experiment Video

Updated: Jun 15, 2026

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
06:24

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal

Published on: October 31, 2019

"Switchable water": aqueous solutions of switchable ionic strength.

Sean M Mercer1, Philip G Jessop

  • 1Department of Chemistry, Queen's University, Kingston, Ontario, Canada.

Chemsuschem
|February 27, 2010
PubMed
Summary
This summary is machine-generated.

Researchers developed switchable ionic strength solutions for greener chemical separations. This method reversibly "salts out" organic compounds from water, avoiding the unsustainable salt waste of traditional methods.

More Related Videos

Generation and Control of Electrohydrodynamic Flows in Aqueous Electrolyte Solutions
08:41

Generation and Control of Electrohydrodynamic Flows in Aqueous Electrolyte Solutions

Published on: September 7, 2018

Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone
08:06

Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone

Published on: February 23, 2017

Related Experiment Videos

Last Updated: Jun 15, 2026

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
06:24

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal

Published on: October 31, 2019

Generation and Control of Electrohydrodynamic Flows in Aqueous Electrolyte Solutions
08:41

Generation and Control of Electrohydrodynamic Flows in Aqueous Electrolyte Solutions

Published on: September 7, 2018

Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone
08:06

Merging Ion Concentration Polarization between Juxtaposed Ion Exchange Membranes to Block the Propagation of the Polarization Zone

Published on: February 23, 2017

Area of Science:

  • Green Chemistry
  • Separation Science
  • Sustainable Chemical Processes

Background:

  • Traditional "salting out" separates water-soluble organics but creates unsustainable salty wastewater.
  • A need exists for environmentally friendly separation techniques with reduced waste generation.

Purpose of the Study:

  • To introduce a novel method for reversible "salting out" using switchable ionic strength solutions.
  • To demonstrate a sustainable alternative to conventional salting out processes.

Main Methods:

  • Utilizing aqueous solutions of diamine in water, which exhibit switchable ionic strength upon CO(2) addition.
  • Applying this switchable ionic strength system to achieve reversible salting out of tetrahydrofuran (THF) from water.

Main Results:

  • Demonstrated that CO(2) addition to diamine-aqueous solutions reversibly increases ionic strength.
  • Successfully applied this system for the reversible separation of THF from water, showcasing the feasibility of the approach.

Conclusions:

  • Developed a sustainable and reversible "salting out" method based on switchable ionic strength.
  • This approach offers a greener alternative for separating water-soluble organic compounds, mitigating the environmental impact of traditional methods.