In the Derjaguin-Landau-Verwey-Overbeek (DLVO) framework of the past 60 years, colloidal interaction between similarly charged particles has been claimed to be simply repulsive, and an attraction such as the van der Waals interaction is attached to the Coulombic repulsion. Statistical-thermodynamic considerations show that the electrostatic Helmholtz free energy ΔF(el) is generally not equal to the electrostatic Gibbs free energy ΔG(el) for simple ionic solutions, and the difference ΔG(el) -ΔF(el) (corresponding to the electrostatic osmotic pressure p(el) ) becomes larger with increasing charge number. Thus, it is expected that ΔG(el) -ΔF(el) be large for highly charged macroions. In the DLVO framework, however, ΔG(el) = ΔF(el) was postulated. Sogami showed that a mean field approach reproduced repulsion at the level of ΔF(el) but resulted in (repulsion and) attraction at the level of ΔG(el) . Overbeek's critique of Sogami theory is shown to be in error. If this criticism were correct, then not only the Sogami theory but also the Debye-Hückel theory would be wrong. The attraction is thus confirmed to exist not only for multi-valent but also mono-valent counterions.
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http://dx.doi.org/10.2183/pjab/83.192 | DOI Listing |
ACS Nano
July 2024
Pacific Northwest National Laboratory, Richland, Washington 99354, United States.
Oriented attachment (OA) occurs when nanoparticles in solution align their crystallographic axes prior to colliding and subsequently fuse into single crystals. Traditional colloidal theories such as DLVO provide a framework for evaluating OA but fail to capture key particle interactions due to the atomistic details of both the crystal structure and the interfacial solution structure. Using zinc oxide as a model system, we investigated the effect of the solvent on short-ranged and long-ranged particle interactions and the resulting OA mechanism.
View Article and Find Full Text PDFJ Cereb Blood Flow Metab
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Department of Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Ischemic lesion net water uptake (NWU) represents a quantitative imaging biomarker for cerebral edema in acute ischemic stroke. Data on NWU for distinct occlusion locations remain scarce, but might help to improve the prognostic value of NWU. In this retrospective multicenter cohort study, we compared NWU between patients with proximal large vessel occlusion (pLVO; ICA or proximal M1) and distal large vessel occlusion (dLVO; distal M1 or M2).
View Article and Find Full Text PDFNanoscale
November 2023
Leibniz-Institut für Polymerforschung Dresden e.V., Institut für Physikalische Chemie und Physik der Polymere, D-01069 Dresden, Germany.
We achieved external activation of local hot-spot sites in supracolloidal assembly structures. The concept was demonstrated by boosting surface-enhanced Raman scattering (SERS) efficiency by one order of magnitude through a heating-induced process. Our approach involves assembling gold nanoparticles with distinct dimensions, 16 and 80 nm, into well-defined planet-satellite-type arrangement structures using thermoresponsive (poly(-isopropylacrylamide)) star polymer linkers.
View Article and Find Full Text PDFJ Colloid Interface Sci
May 2023
Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8572, Japan.
Hypothesis: The classical Schulze-Hardy rule states that the critical coagulation concentration (CCC) of colloidal particles is inversely proportional to the counter-ionic valence at powers ranging from 2 to 6. However, the inverse Schulze-Hardy rule has recently been proposed, suggesting that the CCC can also be inversely proportional to the co-ionic valence. Previous studies on these rules did not consider the effect of flow on aggregation kinetics and the CCC.
View Article and Find Full Text PDFPhys Rev E
July 2022
Department of Physics, Bilkent University, Ankara 06800, Turkey.
The Derjaguin-Landau-Verywey-Overbeek (DLVO) theory has been a remarkably accurate framework for the characterization of macromolecular stability in water solvent. In view of its solvent-implicit nature neglecting the electrostatics of water molecules with non-negligible charge structure and concentration, the precision of the DLVO formalism is somewhat puzzling. In order to shed light on this issue, we derive from our earlier explicit solvent formalism [S.
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