Finite ion size effect on the stability ratio of colloidal dispersions

2020 ◽  
Vol 298 (8) ◽  
pp. 1113-1117
Author(s):  
Hiroyuki Ohshima
RSC Advances ◽  
2021 ◽  
Vol 11 (26) ◽  
pp. 15701-15709
Author(s):  
Siyu Hu ◽  
Anchi Yu ◽  
Rong Lu

The ion size effect on graphitic carbon nitride is responsible for variations in its structure, optical and electronic properties, and hence the enhancement in photocatalytic hydrogen evolution.


2016 ◽  
Vol 13 (10) ◽  
pp. 1050-1058 ◽  
Author(s):  
Hung-Chun Yeh ◽  
Chih-Chang Chang ◽  
Ruey-Jen Yang

2017 ◽  
Vol 199 ◽  
pp. 335-347 ◽  
Author(s):  
V. Sénéchal ◽  
H. Saadaoui ◽  
J. Rodriguez-Hernandez ◽  
C. Drummond

The anchoring of polymer chains at solid surfaces is an efficient way to modify interfacial properties like the stability and rheology of colloidal dispersions, lubrication and biocompatibility. Polyelectrolytes are good candidates for the building of smart materials, as the polyion chain conformation can often be tuned by manipulation of different physico-chemical variables. However, achieving efficient and reversible control of this process represents an important technological challenge. In this regard, the application of an external electrical stimulus on polyelectrolytes seems to be a convenient control strategy, for several reasons. First, it is relatively easy to apply an electric field to the material with adequate spatiotemporal control. In addition, in contrast to chemically induced changes, the molecular response to a changing electric field occurs relatively quickly. If the system is properly designed, this response can then be used to control the magnitude of surface properties. In this work we discuss the effect of an external electric field on the adhesion and lubrication properties of several polyelectrolyte-coated surfaces. The influence of the applied field is investigated at different pH and salt conditions, as the polyelectrolyte conformation is sensitive to these variables. We show that it is possible to fine tune friction and adhesion using relatively low applied fields.


1993 ◽  
Vol 27 (10) ◽  
pp. 117-129 ◽  
Author(s):  
Raj Rajagopalan

The classical theory of coagulation relies on relating the rate of interparticle collisions to the interaction forces, and thus to the physical and chemical parameters of the dispersion, through kinetic arguments, and is restricted to dilute systems. Here, we present a modern, thermodynamic theory capable of predicting stability diagrams for dense as well as dilute dispersions. Although based on statistical thermodynamics, the method is simple to use and requires only the second virial coefficient of osmotic pressure of the dispersion. All the information necessary for applying the model to arbitrary dispersions is given. The method is illustrated for a model colloidal potential, and it is shown how static light scattering measurements can be used for predicting the stability diagrams when information about the colloidal forces are not known in advance.


Sign in / Sign up

Export Citation Format

Share Document