Fractional Walden rule for electrolytes in supercooled disaccharide aqueous solutions

The electrical conductivity of CsCl, KCl, Bu4NBr, and Bu 4NI was studied in stable and supercooled (metastable) sucrose and trehalose aqueous solutions over a wide viscosity range. The results indicate that large positive deviations from the Walden rule occur in these systems due to the higher tende...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Longinotti, Maria Paula, Corti, Horacio Roberto
Publicado: 2009
Materias:
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15206106_v113_n16_p5500_Longinotti
http://hdl.handle.net/20.500.12110/paper_15206106_v113_n16_p5500_Longinotti
Aporte de:
id paper:paper_15206106_v113_n16_p5500_Longinotti
record_format dspace
spelling paper:paper_15206106_v113_n16_p5500_Longinotti2023-06-08T16:19:00Z Fractional Walden rule for electrolytes in supercooled disaccharide aqueous solutions Longinotti, Maria Paula Corti, Horacio Roberto Carbohydrates Ceramic capacitors Dielectric waveguides Electric conductivity Electrolytes Ionization of liquids Ions Permittivity Polysaccharides Sodium chloride Sugar (sucrose) Supercooling Viscosity Aqueous solutions Bulk solutions Dielectric constants Dielectric friction Diffusion of water Effective dielectric constants Electrical conductivity Ion-ion interaction Ionic sizes Ionic solutes Molar conductivities Trehalose aqueous solutions Solutions The electrical conductivity of CsCl, KCl, Bu4NBr, and Bu 4NI was studied in stable and supercooled (metastable) sucrose and trehalose aqueous solutions over a wide viscosity range. The results indicate that large positive deviations from the Walden rule occur in these systems due to the higher tendency of the ions to move in water-rich regions, as previously observed for NaCl and MgCl2. The electrical molar conductivity viscosity dependence can be described with a fractional Walden rule (Ληα = constant), where α is a decoupling parameter which increases with ionic size and varies between 0.61 and 0.74 for all of the studied electrolytes. Using the electrical molar conductivity dependence of ion-ion interactions, an effective dielectric constant was calculated for a trehalose 39 wt% aqueous solution as a function of temperature. Above 278 K, the effective and the bulk solution dielectric constants are similar, but at lower temperatures, where the carbohydrate becomes less mobile than water, the effective dielectric constant approaches the dielectric constant of water. We also conclude that the solute-solvent dielectric friction contribution can be neglected, reinforcing the idea that the observed breakdown of the Walden rule is due to the existence of local microheterogeneities. The Walden plots for the studied ionic solutes show a decoupling similar to that found for the diffusion of water in the same solutions. © 2009 American Chemical Society. Fil:Longinotti, M.P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Corti, H.R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2009 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15206106_v113_n16_p5500_Longinotti http://hdl.handle.net/20.500.12110/paper_15206106_v113_n16_p5500_Longinotti
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Carbohydrates
Ceramic capacitors
Dielectric waveguides
Electric conductivity
Electrolytes
Ionization of liquids
Ions
Permittivity
Polysaccharides
Sodium chloride
Sugar (sucrose)
Supercooling
Viscosity
Aqueous solutions
Bulk solutions
Dielectric constants
Dielectric friction
Diffusion of water
Effective dielectric constants
Electrical conductivity
Ion-ion interaction
Ionic sizes
Ionic solutes
Molar conductivities
Trehalose aqueous solutions
Solutions
spellingShingle Carbohydrates
Ceramic capacitors
Dielectric waveguides
Electric conductivity
Electrolytes
Ionization of liquids
Ions
Permittivity
Polysaccharides
Sodium chloride
Sugar (sucrose)
Supercooling
Viscosity
Aqueous solutions
Bulk solutions
Dielectric constants
Dielectric friction
Diffusion of water
Effective dielectric constants
Electrical conductivity
Ion-ion interaction
Ionic sizes
Ionic solutes
Molar conductivities
Trehalose aqueous solutions
Solutions
Longinotti, Maria Paula
Corti, Horacio Roberto
Fractional Walden rule for electrolytes in supercooled disaccharide aqueous solutions
topic_facet Carbohydrates
Ceramic capacitors
Dielectric waveguides
Electric conductivity
Electrolytes
Ionization of liquids
Ions
Permittivity
Polysaccharides
Sodium chloride
Sugar (sucrose)
Supercooling
Viscosity
Aqueous solutions
Bulk solutions
Dielectric constants
Dielectric friction
Diffusion of water
Effective dielectric constants
Electrical conductivity
Ion-ion interaction
Ionic sizes
Ionic solutes
Molar conductivities
Trehalose aqueous solutions
Solutions
description The electrical conductivity of CsCl, KCl, Bu4NBr, and Bu 4NI was studied in stable and supercooled (metastable) sucrose and trehalose aqueous solutions over a wide viscosity range. The results indicate that large positive deviations from the Walden rule occur in these systems due to the higher tendency of the ions to move in water-rich regions, as previously observed for NaCl and MgCl2. The electrical molar conductivity viscosity dependence can be described with a fractional Walden rule (Ληα = constant), where α is a decoupling parameter which increases with ionic size and varies between 0.61 and 0.74 for all of the studied electrolytes. Using the electrical molar conductivity dependence of ion-ion interactions, an effective dielectric constant was calculated for a trehalose 39 wt% aqueous solution as a function of temperature. Above 278 K, the effective and the bulk solution dielectric constants are similar, but at lower temperatures, where the carbohydrate becomes less mobile than water, the effective dielectric constant approaches the dielectric constant of water. We also conclude that the solute-solvent dielectric friction contribution can be neglected, reinforcing the idea that the observed breakdown of the Walden rule is due to the existence of local microheterogeneities. The Walden plots for the studied ionic solutes show a decoupling similar to that found for the diffusion of water in the same solutions. © 2009 American Chemical Society.
author Longinotti, Maria Paula
Corti, Horacio Roberto
author_facet Longinotti, Maria Paula
Corti, Horacio Roberto
author_sort Longinotti, Maria Paula
title Fractional Walden rule for electrolytes in supercooled disaccharide aqueous solutions
title_short Fractional Walden rule for electrolytes in supercooled disaccharide aqueous solutions
title_full Fractional Walden rule for electrolytes in supercooled disaccharide aqueous solutions
title_fullStr Fractional Walden rule for electrolytes in supercooled disaccharide aqueous solutions
title_full_unstemmed Fractional Walden rule for electrolytes in supercooled disaccharide aqueous solutions
title_sort fractional walden rule for electrolytes in supercooled disaccharide aqueous solutions
publishDate 2009
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_15206106_v113_n16_p5500_Longinotti
http://hdl.handle.net/20.500.12110/paper_15206106_v113_n16_p5500_Longinotti
work_keys_str_mv AT longinottimariapaula fractionalwaldenruleforelectrolytesinsupercooleddisaccharideaqueoussolutions
AT cortihoracioroberto fractionalwaldenruleforelectrolytesinsupercooleddisaccharideaqueoussolutions
_version_ 1768545112802983936