scholarly journals Electrohydrodynamic Dispersion of Deformable Aerosols in the Presence of an Electric Field and Chemical Reaction Using Taylor Dispersion Model

2011 ◽  
Vol 23 (2) ◽  
pp. 247-257 ◽  
Author(s):  
N. Rudraiah ◽  
N. Devaraju ◽  
Chiu-On Ng
Author(s):  
Chiu-On Ng

An asymptotic analysis is presented for the advection–diffusion transport of a chemical species in flow through a small-diameter tube, where the flow consists of steady and oscillatory components, and the species may undergo linear reversible (phase exchange or wall retention) and irreversible (decay or absorption) reactions at the tube wall. Both developed and transient concentrations are considered in the analysis; the former is governed by the Taylor dispersion model, while the latter is required in order to formulate proper initial data for the developed mean concentration. The various components of the effective dispersion coefficient, valid when the developed state is attained, are derived as functions of the Schmidt number, flow oscillation frequency, phase partitioning and kinetics of the two reactions. Being more general than those available in the literature, this effective dispersion coefficient incorporates the combined effects of wall retention and absorption on the otherwise classical Taylor dispersion mechanism. It is found that if the phase exchange reaction kinetics is strong enough, the dispersion coefficient is probably to be increased by orders of magnitude by changing the tube wall from being non-retentive to being just weakly retentive.


Author(s):  
Ruy Batista Santiago Neto ◽  
Bernhard Lesche

The influence of electric fields on the velocity of the chemical reaction 4HF+SiO 2 →SiF 4 +2H 2 O in aqueous solution is investigated experimentally. The field strengths used were high enough to measure nonlinear effects. The results permit a critical analysis of a theoretical model known in literature. The basic idea of dipole orientation changing the rate of the primary step of the chemical reaction can explain the experimental data, but several important details of the original model had to be changed. The primary step involves two hydrogen fluoride (HF) molecules rather than one, and field screening by mobile ions has a significant influence causing nonlinear effects. The fact that field screening plays an important role implies that electric field-assisted HF etching of silica may by used as an instrument for measuring ion concentrations in highly concentrated electrolytes. The data measured may be well described by a theoretical model based on mean field approximations. The results give an insight into the structure of highly concentrated hydrofluoric acid and also permit a critical analysis of applications of the effect in measuring electric fields written in glass samples by electrothermal poling. The effect may also be used for shaping glass surfaces.


2020 ◽  
Author(s):  
Ruben Hamans ◽  
Matteo Parente ◽  
Andrea Baldi

Plasmonic nanoparticles have recently emerged as promising photocatalysts for light-driven chemical conversions. The illumination of these particles results in the generation of highly energetic charge carriers, elevated surface temperatures, and enhanced electromagnetic fields around them. Distinguishing between these often-overlapping processes is of paramount importance for the rational design of future plasmonic photocatalysts. However, the study of chemical reactions mediated by plasmonic effects is typically performed at the ensemble level and, therefore, limited by the intrinsic heterogeneity of the catalyst particles. Here, we report an in-situ single particle study of a chemical reaction driven solely by plasmonic near-fields. Using super-resolution fluorescence microscopy, we achieve single turnover temporal resolution and ~30 nm spatial resolution. This sub-particle accuracy permits the construction of a clear correlation between the simulated electric field distribution around individual metal nanoparticles and their super-resolved catalytic activity maps. Our results can easily be extended to systems with more complex electric field distributions, thereby guiding the design of future advanced photoactive materials.


2017 ◽  
Vol 8 (3) ◽  
pp. 2329-2336 ◽  
Author(s):  
Giuseppe Cassone ◽  
Fabio Pietrucci ◽  
Franz Saija ◽  
François Guyot ◽  
A. Marco Saitta

By means of state-of-the-art computational approaches, a new fundamental chemical reaction, involving formaldehyde and methane, has been observed when an electric field is applied to liquid methanol.


Nanoscale ◽  
2020 ◽  
Vol 12 (28) ◽  
pp. 15072-15080
Author(s):  
Xingming Zeng ◽  
Sadaf Bashir Khan ◽  
Ayyaz Mahmood ◽  
Shern-Long Lee

The oriented external electric field of a scanning tunneling microscope (STM) has recently been adapted for controlling the chemical reaction and supramolecular phase transition at surfaces with molecular precision.


Science ◽  
2020 ◽  
Vol 370 (6522) ◽  
pp. 1324-1327 ◽  
Author(s):  
Kyle Matsuda ◽  
Luigi De Marco ◽  
Jun-Ru Li ◽  
William G. Tobias ◽  
Giacomo Valtolina ◽  
...  

Full control of molecular interactions, including reactive losses, would open new frontiers in quantum science. We demonstrate extreme tunability of ultracold chemical reaction rates by inducing resonant dipolar interactions by means of an external electric field. We prepared fermionic potassium-rubidium molecules in their first excited rotational state and observed a modulation of the chemical reaction rate by three orders of magnitude as we tuned the electric field strength by a few percent across resonance. In a quasi–two-dimensional geometry, we accurately determined the contributions from the three dominant angular momentum projections of the collisions. Using the resonant features, we shielded the molecules from loss and suppressed the reaction rate by an order of magnitude below the background value, thereby realizing a long-lived sample of polar molecules in large electric fields.


2004 ◽  
Vol 2004.2 (0) ◽  
pp. 415-416
Author(s):  
Koji Kitabayashi ◽  
Atsushi Katatani ◽  
Shgieru Konishi

Sign in / Sign up

Export Citation Format

Share Document