Thermodiffusion of citrate-coated γ-Fe2O3 nanoparticles in aqueous dispersions with tuned counter-ions – anisotropy of the Soret coefficient under a magnetic field. Issue 4 (11th January 2019)
- Record Type:
- Journal Article
- Title:
- Thermodiffusion of citrate-coated γ-Fe2O3 nanoparticles in aqueous dispersions with tuned counter-ions – anisotropy of the Soret coefficient under a magnetic field. Issue 4 (11th January 2019)
- Main Title:
- Thermodiffusion of citrate-coated γ-Fe2O3 nanoparticles in aqueous dispersions with tuned counter-ions – anisotropy of the Soret coefficient under a magnetic field
- Authors:
- Kouyaté, M.
Filomeno, C. L.
Demouchy, G.
Mériguet, G.
Nakamae, S.
Peyre, V.
Roger, M.
Cēbers, A.
Depeyrot, J.
Dubois, E.
Perzynski, R. - Abstract:
- Abstract : Soret coefficient is modulated in sign by the counterion nature and in magnitude by volume fraction and applied magnetic field; single-particle and thermoelectric contributions are sorted out. Abstract : Under a temperature gradient, the direction of thermodiffusion of charged γ-Fe2 O3 nanoparticles (NPs) depends on the nature of the counter-ions present in the dispersion, resulting in either a positive or negative Soret coefficient. Various counter-ions are probed in finely tuned and well characterized dispersions of citrate-coated NPs at comparable concentrations of free ionic species. The Soret coefficient S T is measured in stationary conditions together with the mass-diffusion coefficient D m using a forced Rayleigh scattering method. The strong interparticle repulsion, determined by SAXS, is also attested by the increase of D m with NP volume fraction Φ . The Φ -dependence of S T is analyzed in terms of thermophoretic and thermoelectric contributions of the various ionic species. The obtained single-particle thermophoretic contribution of the NPs (the Eastman entropy of transfer Ŝ NP ) varies linearly with the entropy of transfer of the counter-ions. This is understood in terms of electrostatic contribution and of hydration of the ionic shell surrounding the NPs. Two aqueous dispersions, respectively, with S T > 0 and with S T < 0 are then probed under an applied field H⃑, and an anisotropy of D m and of S T is induced while the in-field system remainsAbstract : Soret coefficient is modulated in sign by the counterion nature and in magnitude by volume fraction and applied magnetic field; single-particle and thermoelectric contributions are sorted out. Abstract : Under a temperature gradient, the direction of thermodiffusion of charged γ-Fe2 O3 nanoparticles (NPs) depends on the nature of the counter-ions present in the dispersion, resulting in either a positive or negative Soret coefficient. Various counter-ions are probed in finely tuned and well characterized dispersions of citrate-coated NPs at comparable concentrations of free ionic species. The Soret coefficient S T is measured in stationary conditions together with the mass-diffusion coefficient D m using a forced Rayleigh scattering method. The strong interparticle repulsion, determined by SAXS, is also attested by the increase of D m with NP volume fraction Φ . The Φ -dependence of S T is analyzed in terms of thermophoretic and thermoelectric contributions of the various ionic species. The obtained single-particle thermophoretic contribution of the NPs (the Eastman entropy of transfer Ŝ NP ) varies linearly with the entropy of transfer of the counter-ions. This is understood in terms of electrostatic contribution and of hydration of the ionic shell surrounding the NPs. Two aqueous dispersions, respectively, with S T > 0 and with S T < 0 are then probed under an applied field H⃑, and an anisotropy of D m and of S T is induced while the in-field system remains monophasic. Whatever the H⃑ -direction (parallel or perpendicular to the gradients and ), the Soret coefficient is modulated keeping the same sign as in zero applied field. In-field experimental determinations are well described using a mean field model of the interparticle magnetic interaction. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 21:Issue 4(2018)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 21:Issue 4(2018)
- Issue Display:
- Volume 21, Issue 4 (2018)
- Year:
- 2018
- Volume:
- 21
- Issue:
- 4
- Issue Sort Value:
- 2018-0021-0004-0000
- Page Start:
- 1895
- Page End:
- 1903
- Publication Date:
- 2019-01-11
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8cp06858e ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9485.xml