Simple models for the trapping of charged particles and macromolecules by diffusiophoresis in salt gradients

TL;DR

This paper models how charged particles and macromolecules can be trapped in salt gradients through diffusiophoresis, revealing that larger particles are more effectively trapped due to their mobility-to-diffusion ratio.

Contribution

It introduces a simple theoretical framework predicting particle trapping behavior in salt gradients, emphasizing the role of size-dependent diffusiophoretic mobility.

Findings

Trapping size range is 1 to 100 micrometres.

Particle density follows a power law of salt concentration.

Larger particles are more effectively trapped due to higher mobility-to-diffusion ratios.

Abstract

We study the trapping of charged particles and macromolecules (such as DNA) in salt gradients in aqueous solutions. The source for the salt gradient can be as simple as a dissolving ionic crystal, as shown by McDermott et al. [Langmuir 28, 15491 (2012)]. Trapping is due to a competition between localisation due to diffusiophoresis in the salt gradient, and spreading out by diffusion. The size of the trap is typically 1 to 100 micrometres. We further predict that at steady state, the particle (macromolecule) number density is a power law of the salt concentration, with an exponent that is the ratio of the diffusiophoretic mobility to the diffusion coefficient of the trapped species. This ratio increases with size and typically becomes much greater than 1 for particles or macromolecules with hydrodynamic radii of hundreds of nanometres and above. Thus large particles or macromolecules are easily caught and trapped at steady state by salt gradients.