Viscous field-aligned water exhibits cubic-ice-like structural motifs

2018 ◽  
Vol 20 (30) ◽  
pp. 19877-19884 ◽  
Author(s):  
J. Matthias Kahk ◽  
Beng Hau Tan ◽  
Claus-Dieter Ohl ◽  
N. Duane Loh

By constraining the orientations of water molecules, strong electric fields can drive the formation of cubic-ice-like motifs in liquid water.

Materials ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1398
Author(s):  
Yong-Qi Zhang ◽  
Xuan Wang ◽  
Ping-Lan Yu ◽  
Wei-Feng Sun

Trimethylolpropane triacrylate (TMPTA) as a photoactive crosslinker is grafted onto hydrophobic nanosilica surface through click chemical reactions of mercapto double bonds to prepare the functionalized nanoparticles (TMPTA-s-SiO2), which are used to develop TMPTA-s-SiO2/XLPE nanocomposites with improvements in mechanical strength and electrical resistance. The expedited aging experiments of water-tree growth are performed with a water-knife electrode and analyzed in consistence with the mechanical performances evaluated by means of dynamic thermo-mechanical analysis (DMA) and tensile stress–strain characteristics. Due to the dense cross-linking network of polyethylene molecular chains formed on the TMPTA-modified surfaces of SiO2 nanofillers, TMPTA-s-SiO2 nanofillers are chemically introduced into XLPE matrix to acquire higher crosslinking degree and connection strength in the amorphous regions between polyethylene lamellae, accounting for the higher water-tree resistance and ameliorated mechanical performances, compared with pure XLPE and neat-SiO2/XLPE nanocomposite. Hydrophilic TMPTA molecules grafted on the nano-SiO2 surface can inhibit the condensation of water molecules into water micro-beads at insulation defects, thus attenuating the damage of water micro-beads to polyethylene configurations under alternating electric fields and thus restricting water-tree growth in amorphous regions. The intensified interfaces between TMPTA-s-SiO2 nanofillers and XLPE matrix limit the segment motions of polyethylene molecular chains and resist the diffusion of water molecules in XLPE amorphous regions, which further contributes to the excellent water-tree resistance of TMPTA-s-SiO2/XLPE nanocomposites.


2000 ◽  
Vol 91 (5) ◽  
pp. 945-951 ◽  
Author(s):  
S. V. Bulyarskii ◽  
N. S. Grushko ◽  
A. V. Zhukov

2016 ◽  
Vol 788 ◽  
Author(s):  
Ehud Yariv ◽  
Itzchak Frankel

When subject to sufficiently strong electric fields, particles and drops suspended in a weakly conducting liquid exhibit spontaneous rotary motion. This so-called Quincke rotation is a fascinating example of nonlinear symmetry-breaking phenomena. To illuminate the rotation of liquid drops we here analyse the asymptotic limit of large electric Reynolds numbers, $\mathit{Re}\gg 1$, within the framework of a two-dimensional Taylor–Melcher electrohydrodynamic model. A non-trivial dominant balance in this singular limit results in both the fluid velocity and surface-charge density scaling as $\mathit{Re}^{-1/2}$. The flow is governed by a self-contained nonlinear boundary-value problem that does not admit a continuous fore–aft symmetric solution, thus necessitating drop rotation. Furthermore, thermodynamic arguments reveal that a fore–aft asymmetric solution exists only when charge relaxation within the suspending liquid is faster than that in the drop. The flow problem possesses both mirror-image (with respect to the direction of the external field) and flow-reversal symmetries; it is transformed into a universal one, independent of the ratios of electric conductivities and dielectric permittivities in the respective drop phase and suspending liquid phase. The rescaled angular velocity is found to depend weakly upon the viscosity ratio. The corresponding numerical solutions of the exact equations indeed collapse at large $\mathit{Re}$ upon the asymptotically calculated universal solution.


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