scholarly journals Breakdown in CO2 and CO2/C2F4 Mixtures at Elevated Temperatures in the Range 1000-4000 K

2019 ◽  
Vol 6 (1) ◽  
pp. 39-42 ◽  
Author(s):  
M. Seeger ◽  
T. Votteler ◽  
S. Pancheshnyi ◽  
J. Carstensen ◽  
A. Garyfallos ◽  
...  

CO<sub>2</sub> is a promising gas for replacement of SF<sub>6</sub> in high voltage circuit breakers. The electric breakdown in CO<sub>2</sub> and mixtures with C<sub>2</sub>F4 from PTFE nozzles is, however, still not fully understood. To understand the electric breakdown in CO<sub>2</sub> and mixtures with C<sub>2</sub>F<sub>4</sub> from PTFE nozzles fundamental parameters like the temperature and pressure dependence of critical electric fields are needed. Data on critical fields is usually available based on simulations only and experimental validation is lacking so far. Our present contribution aims to close this gap and presents experiments where the breakdown fields in uniform and weakly non-uniform electric fields are determined at various temperatures and pressures. The gas temperatures were estimated from measurements with pyrometers. The results are compared to theoretical predictions.

A detailed study has been made of the conditions under which uncharged water drops of radius 60 to 200 μm coalesce or rebound at a clean water/air interface. The variable para-­meters in the system are the drop radius, r , its impact velocity, V i , and the angle of impact, θ i ; and the dependent parameters are the time of contact, T , between a rebounding drop and the water surface, the velocity, V b , and the angle θ b with which it leaves the surface. All these have been measured. Relations are established between the drop radius and the critical values of V i and θ i at which coalescence occurs between uncharged drops and plane or convex water surfaces. Drops impacting at nearly normal incidence remain in contact with the surface for about 1 ms, lose about 95 % of their kinetic energy during impact, and rebound with an effective coefficient of restitution of about 0.2. Drops carrying a net charge and drops polarized in an applied electric field coalesce more readily than uncharged drops of the same size and impact velocity. The magnitudes of the critical charges and critical fields required to cause coalescence are determined as functions of V i , θ i and drop radius. Typically, drops of radius 150 μm impacting at 100 cm/s coalesce if the charge exceeds about 10 -4 e. s. u. or if the field exceeds about 100 V/cm. If the motion of a drop rebounding from a plane water surface is treated as simple harmonic and undamped, one may derive expressions for the depth of the crater, x and the restoring force, F , at any stage, and also for the time of contact. These yield values that are in reasonable accord with experiment. However, the collision is clearly inelastic, and a second solution is obtained when F is assumed to be proportional, not only to the displacement, x , but to x/t . This leads to a slightly different expression for the time of contact and to a calculated energy loss of 84 % compared with the measured value of 95 %. If the drop is to coalesce with the water surface, it must first expel and rupture the intervening air film. Treating the undersurface of the drop as a flattened circular disk, an expression is determined for the minimum thickness, δ, achieved by the film during the period of contact, in terms of V i , θ i and the drop radius r . This predicts values of δ ~ 0.1 μm below which fusion may well take place under the influence of van der Waals forces. Several features of the observed relations between V i , θ i and r are accounted for by this simplified theory, but the behaviour of drops impacting at nearly glancing incidence, and of relatively large, energetic drops impacting nearly normally is not. In the latter case, the observed distortion of the drop is thought to play an important role in permitting more rapid thinning of the air film and, in the case of charged and polarized drops, by producing intense local electric fields that may cause the final rupture.


2011 ◽  
Vol 493-494 ◽  
pp. 170-174
Author(s):  
Rumi Hiratai ◽  
Miho Nakamura ◽  
Akiko Nagai ◽  
Kimihiro Yamashita

We have shown that hydroxyapatite (HA), which characteristics were similar to those of bone’s inorganic components, had polarization capability and was possible to accumulate electricity under high temperature and pressure. Then, we presumed that bones had polarization capability which enabled electrical storage and conducted the experiment to measure the polarization capability of bones using rabbit’s femurs. After preparing and polarizing bone samples using KOH treatment (koh), KOH and baking treatment (koh+bake) and decalcification treatment (decalcification) as well as the bone without any treatment (untreat), quantitative amounts of stored charge in samples were determined by thermally stimulated depolarization current (TSDC) measurement of these samples. Under the condition of 400 °C for 1 h with the electric fields of 5kV/cm, samples of koh, koh+bake, and untreat showed polarization capability. In addition, under the polarization condition of 37 °C for 1 hour with the electric fields of 5kV/cm, all samples showed polarization capability. Those findings can be summarized that bones have the polarization capability which enables electrical storage and polarization of bones is possible even under the low temperature condition, which was at 37 °C in our experiment, where polarization is impossible for HA.


2020 ◽  
Author(s):  
Andrew J. McNeece ◽  
Margaret L. Kelty ◽  
Alexander S. Filatov ◽  
John Anderson

<div>Local electric fields have recently been investigated for optimizing reactivity in synthetic systems. However, disentangling the relative contributions of inductive (through-bond) and electrostatic (through-space) effects in molecular systems has been a long-standing challenge. To understand the interplay of these effects and leverage electrostatic influences for enhanced reactivity, we have synthesized a distally charged phosphine, Ph<sub>2</sub>PCH<sub>2</sub>BF<sub>3</sub><sup>−</sup>, and studied the effect of the charged trifluoroborate group on its donor properties and reactivity. This charged phosphine displays solvent-dependent changes in donor strength as measured by the <i>J</i><sub>P-Se</sub> of the corresponding phosphine selenide. The variation with solvent dielectric illustrates a significant electrostatic component to the donor strength. Computations further support the importance of electrostatic contributions and highlight the effect of charge position and orientation. Finally, this charged group also greatly accelerates C–F oxidative addition reactivity in Ni complexes, experimentally</div><div>verifying recent theoretical predictions. These results show that covalently bound charged functionalities can exert a significant electrostatic influence even under common solution phase reaction conditions.</div>


Polymers ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 62 ◽  
Author(s):  
Xin-Dong Zhao ◽  
Hong Zhao ◽  
Wei-Feng Sun

Direct current (DC) electrical performances of crosslinked polyethylene (XLPE) have been evidently improved by developing graft modification technique with ultraviolet (UV) photon-initiation. Maleic anhydride (MAH) molecules with characteristic cyclic anhydride were successfully grafted to polyethylene molecules under UV irradiation, which can be efficiently realized in industrial cable production. The complying laws of electrical current varying with electric field and the Weibull statistics of dielectric breakdown strength at altered temperature for cable operation were analyzed to study the underlying mechanism of improving electrical insulation performances. Compared with pure XLPE, the appreciably decreased electrical conductivity and enhanced breakdown strength were achieved in XLPE-graft-MAH. The critical electric fields of the electrical conduction altering from ohm conductance to trap-limited mechanism significantly decrease with the increased testing temperature, which, however, can be remarkably raised by grafting MAH. At elevated temperatures, the dominant carrier transport mechanism of pure XLPE alters from Poole–Frenkel effect to Schottky injection, while and XLPE-graft-MAH materials persist in the electrical conductance dominated by Poole–Frenkel effect. The polar group of grafted MAH renders deep traps for charge carriers in XLPE-graft-MAH, and accordingly elevate the charge injection barrier and reduce charge mobility, resulting in the suppression of DC electrical conductance and the remarkable amelioration of insulation strength. The well agreement of experimental results with the quantum mechanics calculations suggests a prospective strategy of UV initiation for polar-molecule-grafting modification in the development of high-voltage DC cable materials.


2018 ◽  
Vol 58 (1) ◽  
pp. 112
Author(s):  
Son Ly ◽  
Xiao Yu ◽  
Xinsong Zhang ◽  
Alireza Salmachi

High performance water-based drilling fluid alternatives that meet performance objectives with minimal environmental impact must continually be developed. Drilling fluid performance is dependent on fluid characteristics, and among those most critical are viscosity and filtration. One avenue to improve drilling fluid performance is through enhancement by use of potent, water-soluble natural polymers. Psyllium husk powder is an environmentally friendly natural polymer derived from ground-up surfaces of psyllium seeds (Plantago ovata). When in contact with water, psyllium husk powder forms a gel-like, extraordinarily viscous substance at very low concentrations. It was previously shown that pure psyllium husk is an excellent viscosity and filtration agent for water-based drilling fluid under standard conditions. Psyllium husk can also be used as a clay-extender to enhance viscosity and filtration performance of bentonite mud; however, further laboratory testing of this performance enhancement under elevated temperatures and pressures is required. Extensive laboratory experiments were therefore conducted to test husk performance in bentonite mud under such conditions. An electronic rheometer and a temperature and pressure adjustable API filter press were used to evaluate viscoelastic and filtration mud characteristics respectively. Concentrations of 0.05–0.4% husk with 5% bentonite were tested at 25−120°C under 1500 psi. An optimal husk concentration of 0.1% was determined, increasing bentonite viscosity and yield point by up to 46.9% and 68.1% respectively. Filtrate loss rate and filtration cake thickness were reduced by up to 25.8% and 35.3% respectively. The optimal concentration was useable up to 70°C (~2800 m) before deflocculating was required.


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