skip to main content


Title: THE ACCOMMODATION COEFFICIENT OF SALINE SESSILE WATER DROPLETS EVAPORATING WITH VARYING NON-VOLATILE IMPURITY LOADS
Air-water evaporation systems are ubiquitous in industrial applications, including processes such as fuel combustion, inkjet printing, spray cooling, and desalination. In these evaporation-driven systems, a fundamental understanding of mass accommodation at the liquid-vapour interface is critical to predicting and optimizing performance. Interfacial mass accommodation depends on many factors, such as temperature, vapour concentration, non-volatile impurity content, and non-condensable gasses present. Elucidating how these factors interact is essential to designing devices to meet demanding applications. Hence, high precision measurements are needed to quantify accommodation at the liquid-vapour interface accurately. Our previous study has shown surface averaged accommodation coefficients close to 0.001 for pure water droplets throughout evaporation. While it is well established that saline non-volatile impurities reduce the evaporation rate of sessile droplets, the dynamic effect on mass accommodation during the droplet's lifespan is yet to be determined. In this work, we combine experimental and computational techniques to determine the accommodation coefficient over the lifespan of 10-3 to 1 molar potassium chloride-water droplets evaporating on a gold-coated surface into dry nitrogen. This study uses a quartz crystal microbalance as a high-precision contact area sensor. It also determines the non-volatile impurities in the droplet with a precision on the order of nanograms. The computational model couples macroscopic measurements with the microscopic kinetic theory of gasses to quantify hard-to-measure physical quantities. We believe this study will provide a basis for predicting evaporative device performance in conditions where non-volatile impurities are intrinsic to the application.  more » « less
Award ID(s):
1944323
NSF-PAR ID:
10309482
Author(s) / Creator(s):
;
Editor(s):
Meyer, J. P.
Date Published:
Journal Name:
15th International Conference on Heat Transfer, Fluid Mechanics and Thermodynamics
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Markides, C. N. (Ed.)
    Designing air-water systems for industrial applications requires a fundamental understanding of mass accommodation at the liquid-vapor interface, which depends on many factors, including temperature, vapor concentration, and impurities that vary with time. Hence, understanding how mass accommodation changes over a droplet’s lifespan is critical for predicting the performance of applications leveraging evaporation. In this study, experimental data of water droplets on a gold-coated surface evaporating into dry nitrogen is coupled with a computational model to measure the accommodation coefficient at the liquid-vapor interface. We conduct this measurement by combining macroscopic observations with the microscopic kinetic theory of gasses. The experiments utilize a sensitive piezoelectric device to determine the droplet radius with high accuracy and imaging to measure the droplet contact angle. This setup also quantifies the trace amounts of non-volatile impurities in the droplet. For water droplets evaporating in a pure nitrogen stream, the accommodation coefficient directly relates to vapor flux over the droplet’s surface and is affected by the presence of impurities. We obtained a surface-averaged accommodation coefficient close to 0.001 across multiple water droplets evaporating close to room temperature. This quantification can aid in conducting a more accurate analysis of evaporation, which can assist in the improved design of evaporation-based applications. We believe the modeling approach presented in this work, which integrates the kinetic theory of gases to the macroscale flow behavior, can provide a basis for predicting evaporation kinetics in the presence of extremely dry non-condensable gas streams. 
    more » « less
  2. Abstract. This study presents a characterization of the hygroscopic growth behaviour and effects of different inorganic seed particles on the formation of secondary organic aerosols (SOAs) from the dark ozone-initiated oxidation of isoprene at low NOx conditions. We performed simulations of isoprene oxidation using a gas-phase chemical reaction mechanism based onthe Master Chemical Mechanism (MCM) in combination with an equilibriumgas–particle partitioning model to predict the SOA concentration. Theequilibrium model accounts for non-ideal mixing in liquid phases, includingliquid–liquid phase separation (LLPS), and is based on the AIOMFAC (Aerosol Inorganic–Organic Mixtures Functional groups Activity Coefficients) model for mixture non-ideality and the EVAPORATION (Estimation of VApour Pressure of ORganics, Accounting for Temperature,Intramolecular, and Non-additivity effects) model for pure compound vapourpressures. Measurements from the Cosmics Leaving Outdoor Droplets (CLOUD)chamber experiments, conducted at the European Organization for NuclearResearch (CERN) for isoprene ozonolysis cases, were used to aid inparameterizing the SOA yields at different atmospherically relevanttemperatures, relative humidity (RH), and reacted isoprene concentrations. To represent the isoprene-ozonolysis-derived SOA, a selection of organicsurrogate species is introduced in the coupled modelling system. The modelpredicts a single, homogeneously mixed particle phase at all relativehumidity levels for SOA formation in the absence of any inorganic seedparticles. In the presence of aqueous sulfuric acid or ammonium bisulfateseed particles, the model predicts LLPS to occur below ∼ 80 % RH, where the particles consist of an inorganic-rich liquid phase andan organic-rich liquid phase; however, this includes significant amounts of bisulfate and water partitioned to the organic-rich phase. The measurements show an enhancement in the SOA amounts at 85 % RH, compared to 35 % RH, for both the seed-free and seeded cases. The model predictions of RH-dependent SOA yield enhancements at 85 % RH vs. 35 % RH are 1.80 for a seed-free case, 1.52 for the case with ammonium bisulfate seed, and 1.06 for the case with sulfuric acid seed. Predicted SOA yields are enhanced in the presence of an aqueous inorganic seed, regardless of the seed type (ammonium sulfate, ammonium bisulfate, or sulfuric acid) in comparison with seed-free conditions at the same RH level. We discuss the comparison of model-predicted SOA yields with a selection of other laboratory studies on isoprene SOA formation conducted at different temperatures and for a variety of reacted isoprene concentrations. Those studies were conducted at RH levels at or below 40 % with reported SOA mass yields ranging from 0.3 % up to 9.0 %, indicating considerable variations. A robust feature of our associated gas–particle partitioning calculations covering the whole RH range is the predicted enhancement of SOA yield at high RH (> 80 %) compared to low RH (dry) conditions, which is explained by the effect of particle water uptake and its impact on the equilibrium partitioning of all components. 
    more » « less
  3. Abstract

    Lubricant‐infused surfaces (SLIPSs/LISs) enable omniphobicity by reducing droplet pinning through creation of an atomically smooth liquid–liquid interface. Although SLIPSs/LISs provide efficient omniphobicity, the need for lubricant adds additional barriers to heat and mass transport and affects three‐phase contact line dynamics. Here, evaporation dynamics of microscale water droplets on SLIPSs/LISs are investigated using steady and transient methods. Although steady results demonstrate that evaporation on SLIPSs/LISs is identical to solid functional surfaces having equivalent apparent contact angle, transient measurements show significant increases in evaporation timescale. To understand the inconsistency, high‐speed optical imaging is used to study the evaporating droplet free interface. Focal plane shift imaging enables the study of cloaking dynamics by tracking satellite microdroplet motion on the cloaked oil layer to characterize critical timescales. By decoupling the effect of substrate material and working fluid via experiments on both microstructured copper oxide and nanostructured boehmite with water and ethanol, it is demonstrated that lubricant cloaking cannot be predicted purely by thermodynamic considerations. Rather, coalescence dynamics, droplet formation, and surface interactions play important roles on establishing cloaking. The outcomes of this work shed light onto the physics of lubricant cloaking, and provide a powerful experimental platform to characterize droplet interfacial phenomena.

     
    more » « less
  4. The evaporation of droplets on surfaces is a ubiquitous phenomenon essential in nature and industrial applications ranging from thermal management of electronics to self-assembly-based fabrication. In this study, water droplet evaporation on a thin quartz substrate is analyzed using an unsteady two-step arbitrary Lagrangian-Eulerian (ALE) moving mesh model, wherein the evaporation process is simulated during the constant contact radius (CCR) and contact angle (CCA) modes. The numerical model considers mass transfer in the gas domain, flow in the liquid and gas domains, and heat transfer in the solid, liquid, and gas domains. Besides, the model also accounts for interfacial force balance, including thermocapillary stresses, to obtain the instantaneous droplet shape. Experiments involving droplet evaporation on unheated quartz substrates agree with model predictions of contact radius, contact angle, and droplet volume. Model results indicating temperature and velocity distribution across an evaporating water droplet show that the lowest temperatures are at the liquid-gas interface, and a single vortex exists for the predominant duration of the droplet's lifetime. The temperature of the unheated substrate is also significantly reduced due to evaporative cooling. The interfacial evaporation flux distribution, which depends on heat transfer across the droplet and advection in the surrounding medium, shows the highest values near the three-phase contact line. In addition, the model also predicts evaporation dynamics when the substrate is heated and exposed to different advection conditions. Generally, higher evaporation rates result from higher substrate heating and advection rates. However, substrate heating and advection in the surrounding gas have minimal effects on the relative durations of CCR and CCA modes for a given receding contact angle. Specifically, in this case, a 40× increase in substrate heating rate or 7.5× increase in gas velocity can only change these relative durations by 3%. This study also highlights the importance of surface wettability, which affects evaporation dynamics for all the conditions explored by the numerical model. 
    more » « less
  5. Abstract

    Understanding phase transition between the liquid and gaseous states has gained significant interest, and has been ubiquitously observed in many places ranging from natural systems to water–energy nexus and thermal management applications. Phase transition phenomena at liquid–vapor interfaces are greatly governed by intermolecular‐level kinetics, which requires the use of empirical parameters in continuum‐level relations to explain the discrete nature of molecular particles. Despite its significance, it has been a great challenge to find detailed expressions of empirical parameters such as accommodation coefficients, which represent the probabilities for phase transition of liquid or vapor molecules at the interface. Here, direct statistical measurements of accommodation coefficients are reported by tracking the trajectories of liquid and vapor molecules in molecular simulations. The measurements reveal that evaporation and condensation coefficients are different by ≈50%, whereas they have been assumed to be equal in most previous studies. Then, the indirect measurement method is studied from a perspective of theoretical genetics based on the diffusion approximation. A good agreement between two approaches suggests that diffusion approximation can contribute to provide empirical parameters with a cost‐effective method.

     
    more » « less