Measuring evaporation rate constants of highly volatile compounds for use in predictive kinetic models

2021 ◽  
pp. 338932
Author(s):  
Amanda L. Burkhart ◽  
Ruth Waddell Smith ◽  
Victoria L. McGuffin
2012 ◽  
Vol 134 (5) ◽  
Author(s):  
Wei Xu ◽  
Chang-Hwan Choi

In this paper, the evaporation kinetics of microliter-sized sessile droplets of gold colloids (∼250 nm in particle diameters) was experimentally studied on micropatterned superhydrophobic surfaces, compared with those of pure water on a planar hydrophobic surface. The structural microtopography of superhydrophobic surfaces was designed to have a constant air fraction (∼0.8) but varying array patterns including pillars, lines, and wells. During evaporation in a room condition, the superhydrophobic surfaces exhibited a stronger pinning effect than a planar surface, especially in the initial evaporation stage, with significant variations by the surface topographies. Compared to a pure water droplet, colloids exhibited further promoted pinning effects, mainly in the later stage of evaporation. While the well-known evaporative mass transport law of sessile droplets (i.e., linear law of “V2/3∝t”) was generally applicable to the superhydrophobic surfaces, much smaller evaporation rate constants were measured on the patterned superhydrophobic surfaces than on a planar hydrophobic surface. A colloidal droplet further showed lower evaporation rate constants than a pure water droplet as the concentration of particles in the droplets increased over the evaporation. Such transition was more dramatic on a planar surface than on the micropatterned surfaces. Whereas there was no clear correlation between evaporation mode and the evaporation rate observed on the superhydrophobic surfaces, the prominent decrease of the evaporation rate on the planar hydrophobic surface was accompanied with the onset of a second pinning mode.


Separations ◽  
2018 ◽  
Vol 5 (4) ◽  
pp. 47 ◽  
Author(s):  
John McIlroy ◽  
Ruth Smith ◽  
Victoria McGuffin

Forensic fire debris analysis focuses on the identification of a foreign ignitable liquid in debris collected from the scene of a suspected intentional fire. Chromatograms of the extracted debris are compared to a suitable reference collection containing chromatograms of unevaporated and evaporated ignitable liquids. However, there is no standardized method for the evaporation of ignitable liquids and the process itself can be time consuming, which limits the number of chromatograms of evaporated liquids included in the reference collection. This work describes the development and application of a variable-temperature kinetic model to predict evaporation rate constants and mathematically predict chromatograms corresponding to evaporated ignitable liquids. First-order evaporation rate constants were calculated for 78 selected compounds in diesel, which were used to develop predictive models of evaporation rates. Fixed-temperature models were developed to predict the rate constants at five temperatures (5, 10, 20, 30, 35 °C), yielding a mean absolute percent error (MAPE) of 10.0%. The variable-temperature model was then created from these data by multiple linear regression, yielding a MAPE of 16.4%. The model was applied to generate a reference collection of predicted chromatograms of diesel and kerosene corresponding to a range of evaporation levels. Using the modeled reference collection, successful identification of the liquid and level of evaporation in a test set of chromatograms was demonstrated.


2011 ◽  
Vol 63 (6) ◽  
pp. 1177-1182
Author(s):  
Eudes M. Alves ◽  
Paula F. C. Cavalcanti ◽  
Adrianus van Haandel

Increase of pH in polishing ponds can be predicted quantitatively from variations in alkalinity and acidity. These variables are affected by processes that develop simultaneously in ponds: (1) CO2 desorption, (2) biological CO2 removal by photosynthesis and (3) NH3 desorption. An experimental investigation was carried out to determine the desorption rate of carbon dioxide and ammonium. It is shown that CO2 and NH3 desorption can be described by Fick’s law, which describes desorption of a gaseous compounds from water as a first order process with respect to the degree of oversaturation, which is the driving force of the process. An experimental investigation was carried out to determine the desorption rate constants. The value of the constant proved to be inversely proportional to the depth of the pond (H) and its value for H=1 m and at 26°C was established as KCO2=0.34/H d−1 for carbon dioxide and KNH3=0.33/H d−1 for ammonium.


2005 ◽  
Vol 34 (6) ◽  
pp. 758-759 ◽  
Author(s):  
Takayuki Kameda ◽  
Kohei Asano ◽  
Koji Inazu ◽  
Yoshiharu Hisamatsu ◽  
Norimichi Takenaka ◽  
...  

2021 ◽  
pp. 118346
Author(s):  
Dehao Ju ◽  
Li Huang ◽  
Kangping Zhang ◽  
Ming Ye ◽  
Zhong Huang ◽  
...  

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