Air-water interface transport and surface renewal under impacting droplets

Author(s):  
Soken KADOWAKI ◽  
Yasunori WATANABE
2009 ◽  
Vol 36 (16) ◽  
Author(s):  
A. T. Jessup ◽  
W. E. Asher ◽  
M. Atmane ◽  
K. Phadnis ◽  
C. J. Zappa ◽  
...  

2013 ◽  
Vol 733 ◽  
pp. 588-624 ◽  
Author(s):  
Damon E. Turney ◽  
Sanjoy Banerjee

AbstractRates of gas transfer between air and water remain difficult to predict or simulate due to the wide range of length and time scales and lack of experimental observations of near-surface fluid velocity and gas concentrations. The surface renewal model (SR) and surface divergence model (SD) provide the two leading models of the process, yet they remain poorly tested by observation because near-surface velocity is difficult to measure. To contribute to evaluation of these models, we apply new techniques called interfacial particle imaging velocimetry (IPIV) and three-dimensional IPIV (3D-IPIV) for measuring water velocities within a millimetre of a moving deformable air–water interface. The latter technique (3D-IPIV) simultaneously measures the air–water interface topography. We apply these techniques to turbulent open-channel water flows and wind-sheared water flows with microscale breaking waves. Additional measurements made for each flow condition are bulk turbulent length scales, bulk turbulent velocity scales, air–water gas transfer rates, friction velocities, and wave characteristics. We analyse these data to test the surface divergence models for interfacial gas transfer. The first test is of predictions from the Banerjee (Ninth International Heat Transfer Conference, Keynote Lectures, vol. 1, 1990, pp. 395–418, Hemisphere Press) surface divergence model for gas transfer for homogeneous isotropic turbulence interacting with a planar free surface. The second test is of predictions from the McCready, Vassiliadou and Hanratty (AIChE J., vol. 32(7), 1986, pp. 1108–1115) surface divergence model, as applied in both open-channel flow and wind-sheared wavy flows. We find the predictions of the Banerjee and McCreadyet al. models to agree with the experimental data taken for open-channel flow conditions. On the other hand, for wind-driven flows with wind waves we find disagreement between the McCreadyet al. predictions and our direct measurements of the gas transfer coefficient. The cause of the disagreement is investigated by Lagrangian tracking of surface divergence of surface water patches, and by analysis of the corresponding Lagrangian time series with advection–diffusion concepts. A quantitative criterion based on surface divergence strength and lifetime is proposed to distinguish the effectiveness of each near-surface motion toward causing interfacial gas transfer. Capillary waves are found to contribute to surface divergence but to have too short a time scale to cause interfacial gas transfer. As wind speed increases, the presence and intensity on the air–water interface of capillary waves and other ineffective near-surface motions is diminished by the rise of turbulent wakes from microscale breaking waves thus causing the disagreement of the surface divergence model’s predicted transfer rates with measurements. A model of air–water gas transfer that combines the surface renewal and surface divergence models is formulated and found to agree with the data from both open-channel flows and wind-driven flows without requiring an empirical coefficient.


Author(s):  
Randall W. Smith ◽  
John Dash

The structure of the air-water interface forms a boundary layer that involves biological ,chemical geological and physical processes in its formation. Freshwater and sea surface microlayers form at the air-water interface and include a diverse assemblage of organic matter, detritus, microorganisms, plankton and heavy metals. The sampling of microlayers and the examination of components is presently a significant area of study because of the input of anthropogenic materials and their accumulation at the air-water interface. The neustonic organisms present in this environment may be sensitive to the toxic components of these inputs. Hardy reports that over 20 different methods have been developed for sampling of microlayers, primarily for bulk chemical analysis. We report here the examination of microlayer films for the documentation of structure and composition.Baier and Gucinski reported the use of Langmuir-Blogett films obtained on germanium prisms for infrared spectroscopic analysis (IR-ATR) of components. The sampling of microlayers has been done by collecting fi1ms on glass plates and teflon drums, We found that microlayers could be collected on 11 mm glass cover slips by pulling a Langmuir-Blogett film from a surface microlayer. Comparative collections were made on methylcel1ulose filter pads. The films could be air-dried or preserved in Lugol's Iodine Several slicks or surface films were sampled in September, 1987 in Chesapeake Bay, Maryland and in August, 1988 in Sequim Bay, Washington, For glass coverslips the films were air-dried, mounted on SEM pegs, ringed with colloidal silver, and sputter coated with Au-Pd, The Langmuir-Blogett film technique maintained the structure of the microlayer intact for examination, SEM observation and EDS analysis were then used to determine organisms and relative concentrations of heavy metals, using a Link AN 10000 EDS system with an ISI SS40 SEM unit. Typical heavy microlayer films are shown in Figure 3.


2018 ◽  
Author(s):  
Daniel R. Moberg ◽  
Shelby C. Straight ◽  
Francesco Paesani

<div> <div> <div> <p>The temperature dependence of the vibrational sum-frequency generation (vSFG) spectra of the the air/water interface is investigated using many-body molecular dynamics (MB-MD) simulations performed with the MB-pol potential energy function. The total vSFG spectra calculated for different polarization combinations are then analyzed in terms of molecular auto-correlation and cross-correlation contributions. To provide molecular-level insights into interfacial hydrogen-bonding topologies, which give rise to specific spectroscopic features, the vSFG spectra are further investigated by separating contributions associated with water molecules donating 0, 1, or 2 hydrogen bonds to neighboring water molecules. This analysis suggests that the low frequency shoulder of the free OH peak which appears at ∼3600 cm−1 is primarily due to intermolecular couplings between both singly and doubly hydrogen-bonded molecules. </p> </div> </div> </div>


Sign in / Sign up

Export Citation Format

Share Document