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| Main Authors: | , |
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| Format: | Preprint |
| Published: |
2026
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2604.00262 |
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| _version_ | 1866913109220786176 |
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| author | Dean, David S. Diamant, Haim |
| author_facet | Dean, David S. Diamant, Haim |
| contents | Transport coefficients and dielectric relaxation in liquids are often treated as distinct manifestations of molecular dynamics. We show that, in polar liquids, orientational dipolar fluctuations generate a substantial contribution to the shear viscosity that can be expressed in terms of dielectric response parameters. Using a Green-Kubo approach formulated in terms of dipolar body-force correlations, we derive an explicit relation linking the viscosity increment to the static permittivity and the Debye relaxation time. With a single microscopic cutoff length fixed from one temperature, the theory predicts the temperature dependence of the viscosity for water and several alcohols using independently measured dielectric data. The results identify a general mechanism by which slow polarization dynamics generate an additional, and in strongly polar liquids often dominant, contribution to the viscosity, providing a quantitative bridge between dielectric spectroscopy and rheology. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2604_00262 |
| institution | arXiv |
| publishDate | 2026 |
| record_format | arxiv |
| spellingShingle | Dielectric response as a source of viscosity in polar liquids Dean, David S. Diamant, Haim Statistical Mechanics Transport coefficients and dielectric relaxation in liquids are often treated as distinct manifestations of molecular dynamics. We show that, in polar liquids, orientational dipolar fluctuations generate a substantial contribution to the shear viscosity that can be expressed in terms of dielectric response parameters. Using a Green-Kubo approach formulated in terms of dipolar body-force correlations, we derive an explicit relation linking the viscosity increment to the static permittivity and the Debye relaxation time. With a single microscopic cutoff length fixed from one temperature, the theory predicts the temperature dependence of the viscosity for water and several alcohols using independently measured dielectric data. The results identify a general mechanism by which slow polarization dynamics generate an additional, and in strongly polar liquids often dominant, contribution to the viscosity, providing a quantitative bridge between dielectric spectroscopy and rheology. |
| title | Dielectric response as a source of viscosity in polar liquids |
| topic | Statistical Mechanics |
| url | https://arxiv.org/abs/2604.00262 |