scholarly journals Response to “Comment on ‘Kinetic theory of the stability of the inhomogeneous plasmas with transverse inhomogeneous electric field’ ” [Phys. Plasmas 13, 104703 (2006)]

2006 ◽  
Vol 13 (10) ◽  
pp. 104704 ◽  
Author(s):  
Vladimir S. Mikhailenko
Author(s):  
V.I. Garshin ◽  
◽  
A.R. Lebedev ◽  
S.E. Geraskova ◽  
◽  
...  

The article shows the relations for modeling an inhomogeneous electric field and the flight path of a drop of galvanic electrolyte in it. Estimates are preliminary. Articles and patents of authors in which non-uniform fields are already used are given. A modified trajectory method is proposed for evaluating the effectiveness of trapping harmful electrolyte droplets.


2021 ◽  
Vol 103 (7) ◽  
Author(s):  
K. K. Gowthama ◽  
Manu Kurian ◽  
Vinod Chandra

2017 ◽  
Vol 70 (4) ◽  
pp. 367 ◽  
Author(s):  
Ganna Gryn'ova ◽  
Michelle L. Coote

Accurate quantum-chemical calculations are used to analyze the effects of charges on the kinetics and thermodynamics of radical reactions, with specific attention given to the origin and directionality of the effects. Conventionally, large effects of the charges are expected to occur in systems with pronounced charge-separated resonance contributors. The nature (stabilization or destabilization) and magnitude of these effects thus depend on the orientation of the interacting multipoles. However, we show that a significant component of the stabilizing effects of the external electric field is largely independent of the orientation of external electric field (e.g. a charged functional group, a point charge, or an electrode) and occurs even in the absence of any pre-existing charge separation. This effect arises from polarization of the electron density of the molecule induced by the electric field. This polarization effect is greater for highly delocalized species such as resonance-stabilized radicals and transition states of radical reactions. We show that this effect on the stability of such species is preserved in chemical reaction energies, leading to lower bond-dissociation energies and barrier heights. Finally, our simplified modelling of the diol dehydratase-catalyzed 1,2-hydroxyl shift indicates that such stabilizing polarization is likely to contribute to the catalytic activity of enzymes.


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.


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