Failure of Debye-Hückel Screening in Low-Charge Colloidal Suspensions
Derjaguin–Landau–Verwey–Overbeek (DLVO) theory remains the cornerstone of colloid stability. Electrostatic interactions dominate van der Waals attractions at large colloid-colloid separations h, unless strongly screened. Under these conditions, the potential U ( h )...
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doaj-e79b4fe4c76847d7971e0227cfe8d21f2020-11-24T21:00:31ZengMDPI AGColloids and Interfaces2504-53772018-10-01245110.3390/colloids2040051colloids2040051Failure of Debye-Hückel Screening in Low-Charge Colloidal SuspensionsFranceska Waggett0Mohamad Danial Shafiq1Paul Bartlett2School of Chemistry, University of Bristol, Bristol BS8 1TS, UKSchool of Chemistry, University of Bristol, Bristol BS8 1TS, UKSchool of Chemistry, University of Bristol, Bristol BS8 1TS, UKDerjaguin–Landau–Verwey–Overbeek (DLVO) theory remains the cornerstone of colloid stability. Electrostatic interactions dominate van der Waals attractions at large colloid-colloid separations h, unless strongly screened. Under these conditions, the potential U ( h ) between charged colloids is expected to be exponentially screened, U ( h ) ∼ exp ( − κ h ) / h , with κ − 1 = λ D where λ D is the classical Debye-Hückel screening length. By measuring the force between individual charged particles at dilute electrolyte concentrations (<mM) using optical tweezers, we tested experimentally the prediction κ − 1 = λ D in a nonpolar solvent. At low salt concentrations, we found close agreement between the directly-measured decay length κ − 1 and Debye-Hückel predictions. However, above a critical electrolyte concentration (≈450 μ M), we obtained significant discrepancies between measured and predicted screening lengths, with κ − 1 ≫ λ D . In marked contrast to expectations, we found that the measured screening length κ − 1 appears to grow as the ionic strength of the solution is increased. The origin of this discrepancy is discussed and the importance of considering the surface is highlighted.http://www.mdpi.com/2504-5377/2/4/51electrostaticsDLVOoptical manipulation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Franceska Waggett Mohamad Danial Shafiq Paul Bartlett |
spellingShingle |
Franceska Waggett Mohamad Danial Shafiq Paul Bartlett Failure of Debye-Hückel Screening in Low-Charge Colloidal Suspensions Colloids and Interfaces electrostatics DLVO optical manipulation |
author_facet |
Franceska Waggett Mohamad Danial Shafiq Paul Bartlett |
author_sort |
Franceska Waggett |
title |
Failure of Debye-Hückel Screening in Low-Charge Colloidal Suspensions |
title_short |
Failure of Debye-Hückel Screening in Low-Charge Colloidal Suspensions |
title_full |
Failure of Debye-Hückel Screening in Low-Charge Colloidal Suspensions |
title_fullStr |
Failure of Debye-Hückel Screening in Low-Charge Colloidal Suspensions |
title_full_unstemmed |
Failure of Debye-Hückel Screening in Low-Charge Colloidal Suspensions |
title_sort |
failure of debye-hückel screening in low-charge colloidal suspensions |
publisher |
MDPI AG |
series |
Colloids and Interfaces |
issn |
2504-5377 |
publishDate |
2018-10-01 |
description |
Derjaguin–Landau–Verwey–Overbeek (DLVO) theory remains the cornerstone of colloid stability. Electrostatic interactions dominate van der Waals attractions at large colloid-colloid separations h, unless strongly screened. Under these conditions, the potential U ( h ) between charged colloids is expected to be exponentially screened, U ( h ) ∼ exp ( − κ h ) / h , with κ − 1 = λ D where λ D is the classical Debye-Hückel screening length. By measuring the force between individual charged particles at dilute electrolyte concentrations (<mM) using optical tweezers, we tested experimentally the prediction κ − 1 = λ D in a nonpolar solvent. At low salt concentrations, we found close agreement between the directly-measured decay length κ − 1 and Debye-Hückel predictions. However, above a critical electrolyte concentration (≈450 μ M), we obtained significant discrepancies between measured and predicted screening lengths, with κ − 1 ≫ λ D . In marked contrast to expectations, we found that the measured screening length κ − 1 appears to grow as the ionic strength of the solution is increased. The origin of this discrepancy is discussed and the importance of considering the surface is highlighted. |
topic |
electrostatics DLVO optical manipulation |
url |
http://www.mdpi.com/2504-5377/2/4/51 |
work_keys_str_mv |
AT franceskawaggett failureofdebyehuckelscreeninginlowchargecolloidalsuspensions AT mohamaddanialshafiq failureofdebyehuckelscreeninginlowchargecolloidalsuspensions AT paulbartlett failureofdebyehuckelscreeninginlowchargecolloidalsuspensions |
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1716779493703548928 |