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تسجيل مستخدم جديدHow does the presence of stevia glycosides impact surface bubbles stability?
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The addition of sweeteners in fizzy beverages not only affects the sugar content but also the bubbles stability. In this article, we propose a model experiment, in which the lifetime of hundreds of single bubbles is measured, to assess the stability of bubbles in solutions containing either sucrose or sweeteners. We show that the bubbles are indeed more stable in presence of sweeteners, which are surface active molecules and adsorb at the interface. Additionally, we test an antifoam at different concentrations and show that our experiment allows to identify the best concentration to reproduce the stability obtained in sucrose when we replace this latter by a sweetener.
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Surface bubbles have attracted much interest in the past decades. In this article, we propose to explore the lifetime and thinning dynamics of centimetric surface bubbles. We study the impact of the bubbles size as well as that of the atmospheric hum
idity through a careful control and systematic variation of the relative humidity in the measuring chamber. We first adress the question of the drainage under saturated water vapor conditions and show that a model including both capillary and gravity driven drainage provides the best prediction for this process. Additionally, unprecedented statistics on the bubbles lifetimes confirm experimentally that this parameter is set by evaporation to leading order. We make use of a model based on the overall thinning dynamics of the thin film and assume a rupture thickness of the order 10-100 nm to obtain a good representation of these data. For experiments conducted far from saturation, the convective evaporation of the bath is shown to dominate the overall mass loss in the cap film due to evaporation.
The mass, accretion rate and formation time of dark matter haloes near proto-filaments (identified as saddle points of the potential) are analytically predicted using a conditional version of the excursion set approach in its so-called upcrossing app
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Understanding the critical condition and mechanism of the droplet wetting transition between Cassie-Baxter state and Wenzel state triggered by an external electric field is of considerable importance because of its numerous applications in industry a
nd engineering. However, such a wetting transition on a patterned surface is still not fully understood, e.g., the effects of electro-wetting number, geometry of the patterned surfaces, and droplet volume on the transition have not been systematically investigated. In this paper, we propose a theoretical model for the Cassie-Baxter- Wenzel wetting transition triggered by applying an external voltage on a droplet placed on a mircopillared surface or a porous substrate. It is found that the transition is realized by lowering the energy barrier created by the intermediate composite state considerably, which enables the droplet to cross the energy barrier and complete the transition process. Our calculations also indicate that for fixed droplet volume, the critical electrowetting number (voltage) will increase (decrease) along with the surface roughness for a micro-pillar patterned (porous) surface, and if the surface roughness is fixed, a small droplet tends to ease the critical electrowetting condition for the transition. Besides, three dimensional phase diagrams in terms of electrowetting number, surface roughness, and droplet volume are constructed to illustrate the Cassie-Baxter-Wenzel wetting transition. Our theoretical model can be used to explain the previous experimental results about the Cassie-Baxter-Wenzel wetting transition reported in the literature.
The impact of COVID-19 on students has been enormous, with an increase in worries about fiscal and physical health, a rapid shift to online learning, and increased isolation. In addition to these changes, students with disabilities/health concerns ma
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This work discusses the sedimentation stability and aging of aqueous suspension of Laponite in the presence of cetyltrimethylammonium bromide (CTAB). The concentration of Laponite was fixed at the constant level $C_l=2$ %wt, which corresponds to the
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