Supporting the surface charging mechanism of seismic-electromagnetic phenomena by the direct measurements of the electron and hole trapping centers

Author(s):  
Kiriha Tanaka ◽  
Hiroyuki Nagahama ◽  
Jun Muto ◽  
Toshitaka Oka ◽  
Yasuo Yabe

<p>The mechanisms of the seismic-electromagnetic phenomena (SEP) attracted as precursors of short-term earthquake forecast have been suggested, however, it is still incompletely understood. Among the possible mechanisms of the SEP is the surface charging mechanism related to the electron and hole trapping centers in quartz. Previous studies evaluated the plausibility of the mechanism from the surface charge density by the measurement of current or potential changes. On the other hand, only a few studies have evaluated the plausibility from the direct measurements of the trapping centers’ concentration.</p><p>We have performed low-velocity friction experiments mimicking the fracture with low-frictional heating for simulated fault gouges (commercial natural quartz sands) at a normal stress of 1.0 MPa with displacements up to 1.4 m. In order to measure the concentration of the trapping centers in the simulated-fault gouges, we conducted electron spin resonance for the standard sample, TEMPOL (4-hydroxy-2,2,6,6-tetramethyl-piperidine-1-oxyl), and the gouges before and after friction. In recent decades, researchers also have obtained the concentrations of the trapping centers in the quartz damaged in the rock fracture experiments using ESR and a radical scavenger. From those concentrations with the measured or assumed surface areas, we calculated the surface charge density of the quartz and discussed the plausibility of the surface charging mechanism of the SEP.</p><p>In our friction experiments, the E’ type centers were detected at g<sub>2</sub> = 2.001 (e.g., E<sub>1</sub>’ center; ≡Si・, E<sub>S</sub>’ center; ≡Si・, E<sub>α</sub>’ center; =Si:, where − is an electron pair, : is a lone pair, and ・ is an unpaired electron) in the ESR spectra of the simulated-quartz gouges and the trapping center increased by the fracture of low-velocity friction. Assuming that the trapping centers were produced on the grain surfaces by the fracture, the range of the increase in the surface charge density was (0.21–8.0) ×10<sup>-4</sup> C/m<sup>2</sup>. The rock fracture experiments found the E<sub>1</sub>’ center, non-bridging oxygen hole center (NBOHC; ≡Si−O・), and peroxy center (≡Si−O−O・) in quartz. On the same assumption, the total surface charge density of those trapping centers and the density of the E<sub>1</sub>’ center or NBOHC were estimated as 2.7×10<sup>-1</sup> and 5.0×10<sup>-2</sup>–3.94 C/m<sup>2</sup>, respectively.</p><p>The surface charge density required for a corona discharge that can cause the SEP in the air over a flat plane is reported over 5.0×10<sup>-5</sup> C/m<sup>2</sup>. The quantities calculated above are almost enough to induce a corona discharge. The surface charges can form the electric dipoles on the fault plane, inducing the electric and magnetic fields. Our experiment showed that the fracture by fault motions could produce the surface charges on the fault. It proves that the electromagnetic abnormalities by the fault motions may also be observed through the surface charging mechanism. Therefore, our study supports that the surface charging mechanism is plausible.</p>

2020 ◽  
Vol 22 (35) ◽  
pp. 20123-20142
Author(s):  
Hadi Saboorian-Jooybari ◽  
Zhangxin Chen

This research work is directed at development of accurate physics-based formulas for quantification of curvature-dependence of surface potential, surface charge density, and total surface charge for cylindrical and spherical charged particles immersed in a symmetrical electrolyte solution.


An earlier paper discussed the influence of the shape of a macroscopic piece of ionic crystal on the electrostatic energy of the whole piece of crystal. Some of the considerations of that paper are extended to include the effects on the bulk term in the energy of distributing excess charge on the surface of the piece of crystal. The bulk term in the electrostatic energy of the piece of crystal plus surface charges depends on the shape of the piece and the surface charge density. The minimum of this bulk term with respect to surface charge density occurs at a well defined surface charge density and is the usual (shape-independent) Madelung crystal energy.


1975 ◽  
Vol 66 (1) ◽  
pp. 47-65 ◽  
Author(s):  
T Begenisich

The effects of changes in the concentration of calcium in solutions bathing Myxicola giant axons on the voltage dependence of sodium and potassium conductance and on the instantaneous sodium and potassium current-voltage relations have been measured. The sodium conductance-voltage relation is shifted along the voltage axis by 13 mV in the hyperpolarizing direction for a fourfold decrease in calcium concentration. The potassium conductance-voltage relation is shifted only half as much as that for sodium. There is no effect on the shape of the sodium and potassium instantaneous current-voltage curves: the normal constant-field rectification of potassium currents is maintained and the normal linear relationship of sodium currents is maintained. Considering that shifts in conductances would reflect the presence of surface charges near the gating machinery and that shape changes of instantaneous current-voltage curves would reflect the presence of surface charges near the ionic pores, these results indicate a negative surface charge density of about 1 electronic charge per 120 A2 near the sodium gating machinery, about 1 e/300 A2 for the potassium gating machinery, and much less surface charge near the sodium or potassium pores. There may be some specific binding of calcium to these surface charges with an upper limit on the binding constant of about 0.2 M-1. The differences in surface charge density suggest a spatial separation for these four membrane components.


1987 ◽  
Vol 89 (4) ◽  
pp. 629-644 ◽  
Author(s):  
R S Kass ◽  
D S Krafte

We have measured the density of negative surface charges near the voltage sensor for inactivation gating of (L-type) Ca channels in intact calf Purkinje fibers and in isolated myocytes from guinea pig and rat ventricles. Divalent cation-induced changes in the half-maximal voltage for inactivation were determined and were well described by curves predicted by surface potential theory. We measured shifts in inactivation induced by Ca, Sr, and Ba in the single cells, and by Sr in the Purkinje fibers. All of the data were consistent with an estimated negative surface charge density of 1 electronic charge per 250 A2. In addition, the data suggest that Ca, but neither Ba nor Sr, binds to the negative charges with an association constant on the order of 1 M-1. We find that divalent ion-induced changes in surface potential can account for most of the antagonism between these ions and Ca channel block by 1,4-dihydropyridines.


Author(s):  
Dongyan Xu ◽  
Deyu Li ◽  
Yongsheng Leng ◽  
Yunfei Chen

Fundamental studies in nanofluidics have attracted significant attention in the past decade since the success of nanofluidic devices depends on a thorough understanding of the fluidic, ionic, and molecular behaviors in highly confined nano-environments. In this work, molecular dynamics simulations of the effect of surface charge densities on the ion and water distribution in the near wall region has been performed for both (100) and (111) silicon surfaces. We demonstrate that surface charges not only interact with mobile ions in the electrolyte, but also interact with water molecules due to their polarizability and hence influence the orientation of water molecules close to the charged surface. It is shown that as the surface charge density increases, water molecules within ∼ 5 Å from the (100) silicon surface can evolve from one layer into two layers and meanwhile, the orientation of water molecules is more aligned instead of randomly distributed. However, no extra water layer is observed near a (111) silicon surface even under a surface charge density of as high as −0.2034 C/m2. The above phenomenon may be related to the different surface atom densities of (100) and (111) silicon surfaces.


Cells ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 1519
Author(s):  
Leixin Ouyang ◽  
Rubia Shaik ◽  
Ruiting Xu ◽  
Ge Zhang ◽  
Jiang Zhe

Many bio-functions of cells can be regulated by their surface charge characteristics. Mapping surface charge density in a single cell’s surface is vital to advance the understanding of cell behaviors. This article demonstrates a method of cell surface charge mapping via electrostatic cell–nanoparticle (NP) interactions. Fluorescent nanoparticles (NPs) were used as the marker to investigate single cells’ surface charge distribution. The nanoparticles with opposite charges were electrostatically bonded to the cell surface; a stack of fluorescence distribution on a cell’s surface at a series of vertical distances was imaged and analyzed. By establishing a relationship between fluorescent light intensity and number of nanoparticles, cells’ surface charge distribution was quantified from the fluorescence distribution. Two types of cells, human umbilical vein endothelial cells (HUVECs) and HeLa cells, were tested. From the measured surface charge density of a group of single cells, the average zeta potentials of the two types of cells were obtained, which are in good agreement with the standard electrophoretic light scattering measurement. This method can be used for rapid surface charge mapping of single particles or cells, and can advance cell-surface-charge characterization applications in many biomedical fields.


Author(s):  
Linards Lapčinskis ◽  
Artis Linarts ◽  
Kaspars Mālnieks ◽  
Hyunseung Kim ◽  
Kristaps Rubenis ◽  
...  

In this study, we investigate triboelectrification in polymer-based nanocomposites using identical polymer matrixes containing different concentrations of nanoparticles (NPs). The triboelectric surface charge density on polymer layers increased as the...


2021 ◽  
Vol 22 (5) ◽  
pp. 2270
Author(s):  
Joanna Kotyńska ◽  
Monika Naumowicz

Interactions between phospholipid membranes and selected drugs affecting the central nervous system (CNS) were investigated. Small, unilamellar liposomes were used as biomimetic cell membrane models. Microelectrophoretic experiments on two-component liposomes were performed using the electrophoretic light scattering technique (ELS). The effect of both positively (perphenazine, PF) and negatively (barbituric acid, BA) charged drugs on zwitterionic L-α-phosphatidylcholine (PC) membranes were analyzed. Experimental membrane surface charge density (d) data were determined as a function of pH. Quantitative descriptions of the adsorption equilibria formed due to the binding of solution ions to analyzed two-component membranes are presented. Binding constants of the solution ions with perphenazine and barbituric acid-modified membranes were determined. The results of our research show that both charged drugs change surface charge density values of phosphatidylcholine membranes. It can be concluded that perphenazine and barbituric acid are located near the membrane surface, interacting electrostatically with phosphatidylcholine polar heads.


Nanoscale ◽  
2017 ◽  
Vol 9 (27) ◽  
pp. 9668-9675 ◽  
Author(s):  
Jia Jia Shao ◽  
Wei Tang ◽  
Tao Jiang ◽  
Xiang Yu Chen ◽  
Liang Xu ◽  
...  

A multi-dielectric-layered vertical contact-separation mode TENG through a corona discharge approach results in outstanding output performances, i.e., a high surface charge density of 283 μC m−2 and excellent cycling stability (92.6% retention after 200 000 cycles).


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