Related Experiment Video
Updated: Aug 21, 2026

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)
Published on: November 22, 2016
Criticality in aqueous solutions of 3-methylpyridine and sodium bromide
A F Kostko1, M A Anisimov, J V Sengers
1Institute for Physical Science and Technology, University of Maryland, College Park, Maryland 20742, USA.
Abstract:
We address a controversial issue regarding the nature of critical behavior in ternary electrolyte solutions of water, 3-methylpyridine, and sodium bromide. Earlier light-scattering studies showed an anomalous critical behavior in this system that was attributed to the formation of a microheterogeneous phase associated with ion-molecule clustering [M.A. Anisimov, J. Jacob, A. Kumar, V.A. Agayan, and J. V. Sengers, Phys. Rev. Lett. 85, 2336 (2000)]], while some other investigators subsequently found this system to exhibit ordinary Ising-like critical behavior. This contradiction forced us to revisit the problem and perform an accurate and comprehensive study of light scattering in this system paying attention to the achievement of thermodynamic equilibrium, hysteresis effects, aging, and prehistory of the samples, and a possible role of impurities. We show that properly aged, equilibrium samples of aqueous solutions of 3-methylpyridine with NaBr exhibit universal Ising-like critical behavior, typical for other aqueous solutions. No evidence for an equilibrium microheterogeneous phase was found. We have been able to reproduce anomalous behavior (similar to that reported initially) in a fast run on a freshly prepared sample. We attribute the observed anomalies to mesoscopic nonequilibrium aggregates, possibly associated with supramolecular restructuring in aqueous solutions. To support this conclusion we performed a study of aqueous solutions of 3-methylpyridine without NaBr and have found long-living nonequilibrium states in aqueous solutions of 3-methylpyridine.
Related Concept Videos
Radical Substitution: Allylic Bromination
Nucleophilic Substitution Reactions
In 1896, the German chemist Paul Walden discovered that he could interconvert pure enantiomeric (+) and (-) malic acids through a series of reactions. This conversion suggested the involvement of optical inversion during the substitution reaction. Further, in 1930, Sir Christopher Ingold described for the first time two different forms of nucleophilic substitution reactions, which are known as SN1 (nucleophilic substitution unimolecular) and SN2 (nucleophilic substitution...
Preparation and Reactions of Sulfides
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
Formation of Halohydrin from Alkenes
Radical Anti-Markovnikov Addition to Alkenes: Overview

