Experience in registration of evaporation of liquid drops on a substrate by the capacitive method

This paper presents the results of an experimental study of the dynamics of evaporation of nanofluid droplets based on distilled water with a mass concentration of SiO2 nanoparticles of 0.1%, 0.5%, and 7% lying on a metal surface. The drop height was changed over time using original equipment, which is based on an integrated approach to the combined use of capacitive and optical recording methods. The experimental results show that the change in the height of nanofluid droplets with concentrations of 0.1%, 0.5%, and 7% is linear over the main part of the evaporation time interval. A deviation from the linear law is observed at the final stage, at the time interval of complete evaporation. The time for complete evaporation of droplets of nanofluids with a concentration of 0.1% increases by 20%, for droplets with a concentration of 0.5%, it increased by 28% in comparison with the evaporation of droplets of the base liquid. The particle concentration of 7% does not lead to an increase in the evaporation time of droplets in comparison with the evaporation of low concentration droplets. Before the formation of a jelly-like residue of nanoparticles, the evaporation rate of droplets with a particle concentration of 7% is comparable to the evaporation rate of droplets with a concentration of 0.1%.

Numerical Investigation on the Evaporation Performance of Desulfurization Wastewater in a Spray Drying Tower without Deflectors

The desulfurization wastewater evaporation technology with flue gas has been widely applied to dispose of desulfurization wastewater. This paper investigates the effect of flue gas flow rate and temperature, wastewater flow rate and initial temperature, and droplet size on the evaporation performance of the desulfurization wastewater in a spray drying tower without deflectors. The results show that the flue gas flow rate and temperature affect the evaporation performance of desulfurization wastewater. The larger flow rate and higher temperature of flue gas correspond to the faster evaporation speed and the shorter complete evaporation distance of the wastewater droplet. Decreasing the flow rate and increasing the initial temperature of the desulfurization wastewater is advantageous to enhance the evaporation speed and shorten the complete evaporation distance of the wastewater droplet. Reducing the droplet size is beneficial to improve the evaporation performance of the desulfurization wastewater. The orthogonal test results show that the factors affecting droplet evaporation performance are ranked as follows: flue gas flow rate > wastewater flow rate > flue gas temperature > wastewater initial temperature > droplet size. Considering the evaporation ratio and the complete evaporation distance, the optimal setting is 14.470 kg/s for flue gas flow rate, 385 °C for flue gas temperature, 0.582 kg/s for wastewater flow rate, 25 °C for wastewater initial temperature, and 60 μm for droplet size. These studied results can provide valuable information to improve the operational performance of the desulfurization wastewater evaporation technology with flue gas.

Chamber-based insights into the factors controlling IEPOX SOA yield, composition, and volatility

We present measurements utilizing the Filter Inlet for Gases and Aerosols (FIGAERO) applied to chamber measurements of isoprene-derived epoxydiol (IEPOX) reactive uptake to aqueous acidic particles and associated SOA formation. Similar to recent field observations with the same instrument, we detect two molecular components desorbing from the IEPOX SOA in high abundance: C5H12O4 and C5H10O3. The thermal desorption signal of the former, presumably 2-methyltetrols, exhibits two distinct maxima, suggesting it arises from at least two different SOA components with significantly different effective volatilities. Isothermal evaporation experiments illustrate that the most abundant component giving rise to C5H12O4 is semi-volatile, undergoing nearly complete evaporation within 1 hour, while the second, less volatile, component remains unperturbed and even increases in abundance. We thus confirm, using controlled laboratory studies, recent analyses of ambient SOA measurements showing that IEPOX SOA is of very low volatility and commonly measured IEPOX SOA tracers, such as 2-methyltetrols and C5-alkene triols, result predominantly from artifacts of measurement techniques associated with thermal decomposition and/or hydrolysis. We further show that IEPOX SOA volatility continues to evolve via acidity enhanced accretion chemistry on the timescale of hours, potentially involving both 2-methyltetrols and organosulfates.