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- Levitated droplets (2) (entfernen)
An ionization scheme for fast online mass spectrometric interrogation of levitated droplets is presented. That renewed method comprises the output of an a Er:YAG laser at λ = 2.94 µm which is in resonance with the OH stretch vibration band of solvents like water and alcohols. A temporal pulse width larger than the time needed for pressure redistribution and also above the temperature redistribution time constant was found to lead to soft evaporation/ionization. Despite these mild desorption conditions, no additional postionization is found to be needed. Accordingly, the ionization is found to be very soft resulting in entirely intact analyte ions and concentration dependent cluster ions. Resulting mass spectra of small amino acids and large antibiotics are presented showing the versatility of the introduced technique. Above a critical mass of m ≈ 1 kDa, the formed ions carry multiple charges as it is typical for thermospray or electrospray ionization. The detection technique enables fast contactless analysis of the chemical composition of levitated microreactors and, thus, paves the way for future contactless reaction monitoring.
Coulomb fission of charged droplets (The terms drop and droplet are often used synonymous. Throughout this manuscript, to avoid confusion, the terms drop and droplet will be used for liquid spheres with radii in the millimeter range and the micrometer range, respectively. In our experiments, the first correspond to the parent drop while the latter describes the ejected progeny droplets.) is a wellstudied natural phenomenon. Controlled droplet fission is already successfully employed in several technological applications. Still, since the occurring surface rupture relies on the exact understanding and description of the liquid gas boundary, some details are still under debate. Most empirical systematic studies observe falling micrometer droplets passing through the electric field inside a plate capacitor. This approach, although easily applicable and reliable, limits the experimental degrees of freedom regarding the observable time and the maximum size of the drops and can only be performed in consecutive individual observations of different subsequent drops. Here we present a novel setup to study the field induced breakup of acoustically levitated drops. The design does not bear any restrictions towards the temporal window of observation, and allows handling of drops of a tunable radius ranging from 10 µm to several millimeters and a real-time monitoring of one single drop. Our comprehensive study includes a time resolved visual inspection, laser shadowgraphy, laser induced fluorescence imaging, and ambient mass spectrometric interrogation of the nascent Taylor cone. The results shown for a millimeter sized drop, previously inaccessible for Coulomb fission experiments, are mostly comparable with previous results for smaller drops. The major difference is the time scale and the threshold potential of the drop rupture. Both values, however, resemble theoretically extrapolations to the larger radius. The technique allows for a systematic study of breakup behavior of drops of different charge, material, and size.