Artists, using an empirical knowledge, manage to generate and play with giant soap films and bubbles. Until now, scientific studies of soap films generated at a controlled velocity and without any feeding from the top, studied films of a few square centimeters. The present work aims to present a new setup to generate and characterize giant soap films (2~m $times$ 0.7~m). Our setup is enclosed in a humidity-controlled box of 2.2~m high, 1~m long and 0.75~m large. Soap films are entrained by a fishing line withdrawn out of a bubbling solution at various velocities. We measure the maximum height of the generated soap films, as well as their lifetime, thanks to an automatic detection. This is allowed by light-sensitive resistors collecting the light reflected on the soap films and ensures robust statistical measurements. In the meantime, thickness measurements are performed with a UV-VIS-spectrometer, allowing us to map the soap films thickness over time.
The characterisation of the dynamic properties of viscoelastic monolayers of surfactants at the gasliquid interface is very important in the analysis and prediction of foam stability. With most of the relevant dynamic processes being rapid (thermal fluctuation, film coalescence etc.) it is important to probe interfacial dynamics at high deformation rates. Today, only few techniques allow this, one of them being the characterisation of the propagation of electrocapillary waves on the liquid surface. Traditionally, this technique has been applied in a continuous mode (i.e. at constant frequency) in order to ensure reliable accuracy. Here we explore the possibility to analyse the propagation of an excited pulse in order to access the interfacial properties in one single Fourier treatment over a wide range of frequencies. The main advantage of this approach is that the measurement times and the required liquid volumes can be reduced significantly. This occurs at the cost of precision in the measurement, due partly to the presence of a pronounced resonance of the liquid surface. The pulsed approach may therefore be used to prescan the surface response before a more in-depth scan at constant frequency; or to follow the changes of the interfacial properties during surfactant adsorption.
