Poisson–Boltzmann Electrostatics and Ionic Partition Equilibration of Charged Nanoparticles in Aqueous Media
Most nanoparticles (NPs) dispersed in aqueous media carry a net charge. The ensuing electric field plays a fundamental role in determining the thermodynamic and chemodynamic features of the interactions between NPs and dissolved metal species and their lability and bioavailability in environmental a...
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Published in | Journal of physical chemistry. C Vol. 122; no. 30; pp. 17328 - 17337 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
02.08.2018
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Subjects | |
Online Access | Get full text |
ISSN | 1932-7447 1932-7455 1932-7455 |
DOI | 10.1021/acs.jpcc.8b05168 |
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Abstract | Most nanoparticles (NPs) dispersed in aqueous media carry a net charge. The ensuing electric field plays a fundamental role in determining the thermodynamic and chemodynamic features of the interactions between NPs and dissolved metal species and their lability and bioavailability in environmental and biological matrices. Although increasing attention is being paid to the analysis of metal ion speciation in dispersions of charged complexing NPs, so far the electrostatic features of NPs have only been described on the sole basis of their structural charge properties, that is, the number of (potentially) charged groups they carry. This approach intrinsically ignores the impact of counterion accumulation at/within the particle body/surface during equilibration of the system, which effectively lowers the magnitude of the net NP charge density. Herein, we present the first analysis of the potential profile of NPs after their physicochemical equilibration with the aqueous medium, and we discuss the implications thereof in terms of counterion accumulation within and/or in the vicinity of hard, soft, and core–shell NPs. The focus is on soft or core–soft shell NPs in the thick double layer limit for which bulky Donnan features are not applicable. The new conceptual framework identifies the spatial zone over which divalent counterion accumulation is significant as a function of size, charge density, and type of NP, as well as the ionic strength and electrolyte composition (1–1 and 2–1) of the aqueous medium for the most common case of negatively charged NPs. |
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AbstractList | Most nanoparticles (NPs) dispersed in aqueous media carry a net charge. The ensuing electric field plays a fundamental role in determining the thermodynamic and chemodynamic features of the interactions between NPs and dissolved metal species and their lability and bioavailability in environmental and biological matrices. Although increasing attention is being paid to the analysis of metal ion speciation in dispersions of charged complexing NPs, so far the electrostatic features of NPs have only been described on the sole basis of their structural charge properties, that is, the number of (potentially) charged groups they carry. This approach intrinsically ignores the impact of counterion accumulation at/within the particle body/surface during equilibration of the system, which effectively lowers the magnitude of the net NP charge density. Herein, we present the first analysis of the potential profile of NPs after their physicochemical equilibration with the aqueous medium, and we discuss the implications thereof in terms of counterion accumulation within and/or in the vicinity of hard, soft, and core-shell NPs. The focus is on soft or core-soft shell NPs in the thick double layer limit for which bulky Donnan features are not applicable. The new conceptual framework identifies the spatial zone over which divalent counterion accumulation is significant as a function of size, charge density, and type of NP, as well as the ionic strength and electrolyte composition (1-1 and 2-1) of the aqueous medium for the most common case of negatively charged NPs. |
Author | Duval, Jérôme F. L van Leeuwen, Herman P Town, Raewyn M |
AuthorAffiliation | Wageningen University & Research Université de Lorraine, LIEC, UMR 7360 CNRS Physical Chemistry and Soft Matter Systemic Physiological and Ecotoxicological Research (SPHERE), Department of Biology CNRS, Laboratoire Interdisciplinaire des Environnements Continentaux (LIEC), UMR 7360 CNRS |
AuthorAffiliation_xml | – name: Université de Lorraine, LIEC, UMR 7360 CNRS – name: Wageningen University & Research – name: CNRS, Laboratoire Interdisciplinaire des Environnements Continentaux (LIEC), UMR 7360 CNRS – name: Systemic Physiological and Ecotoxicological Research (SPHERE), Department of Biology – name: Physical Chemistry and Soft Matter |
Author_xml | – sequence: 1 givenname: Jérôme F. L orcidid: 0000-0002-5458-3761 surname: Duval fullname: Duval, Jérôme F. L email: jerome.duval@univ-lorraine.fr organization: Université de Lorraine, LIEC, UMR 7360 CNRS – sequence: 2 givenname: Raewyn M orcidid: 0000-0001-9505-1465 surname: Town fullname: Town, Raewyn M organization: Wageningen University & Research – sequence: 3 givenname: Herman P surname: van Leeuwen fullname: van Leeuwen, Herman P organization: Wageningen University & Research |
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SubjectTerms | bioavailability Chemical Sciences dispersions electric field electrolytes Environmental Sciences ionic strength nanoparticles physical chemistry Physical Chemistry and Soft Matter Physics thermodynamics |
Title | Poisson–Boltzmann Electrostatics and Ionic Partition Equilibration of Charged Nanoparticles in Aqueous Media |
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