The experimental demonstration of Rayleigh instability that results in the breakup of a charged droplet, levitated in a quadrupole trap, has been investigated in the literature, but only scarcely. We report here the asymmetric breakup of a charged drop, levitated in a loose trap, wherein the droplet is stabilized at an off-center location in the trap. This aspect of levitation leads to an asymmetric breakup of the charged drop, predominantly in a direction opposite to that of gravity. In the present work, we report the evidence of successive events of the deformation and breakup of a charged drop and its subsequent relaxation after jet ejection using high-speed imaging at a couple of hundred thousand frames per second. Several relevant aspects of this phenomenon such as the effect of the electrodynamic (ED) trap parameters in terms of the applied potential as well as physical parameters such as the size of the drop, gravity, and conductivity on the characteristics of droplet breakup are explored. A clear effect of the trap strength on the deformation (both symmetric and asymmetric) is observed. Moreover, the cone angle at the pole undergoing asymmetric breakup is almost independent of the applied field investigated in the experiments. All of the experimental observations are compared with numerical simulations carried out using the boundary element method (BEM) in the Stokes flow limit. The BEM simulations are also extended to other experimentally achievable parameters. It is observed that the breakup in our study is mostly field-influenced and not field-induced. A plausible theory for the observations is reported, and a sensitive role of the sign of the charge on the droplet and the sign of the end-cap potential, as well as the off-center location of the droplet in the trap, is elucidated.
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http://dx.doi.org/10.1021/acs.langmuir.9b02547 | DOI Listing |
Anal Chem
December 2024
School of Chemistry, University of Bristol, Bristol BS8 1TS, United Kingdom.
Aerosol droplets are unique microcompartments containing microscopic amounts of material and exhibiting surprising chemical reactivity. Although a diverse set of tools exists to characterize the chemical composition of individual submicron particles in air, comparatively fewer approaches can chemically analyze individual, airborne picolitre droplets. We describe a novel approach for mass spectrometric analysis of individual aqueous picolitre droplets (∼2-180 pL volume) containing down to ∼1 pg analyte mass per droplet.
View Article and Find Full Text PDFGels
September 2024
Chemistry Centre, School of Sciences, University of Minho, 4710-057 Braga, Portugal.
Self-assembly of peptide building blocks offers unique opportunities for bottom-up preparation of exquisite nanostructures, nanoarchitectures, and nanostructured bulk materials, namely hydrogels. In this work we describe the synthesis, characterization, gelation, and rheological properties of new dehydrotripeptides, Cbz--Lys(Cbz)-,-Asp-∆Phe-OH and (2-Naph)--Lys(2-Naph)-,-Asp-∆Phe-OH, containing a -terminal lysine residue --capped with carboxybenzyl (Cbz) and 2-Naphthylacetyl (2-Naph) aromatic moieties, an aspartic acid residue (Asp), and a -terminal dehydrophenylalanine (∆Phe) residue. The dehydrotripeptides were obtained as diastereomeric mixtures (,, and ,,Z), presumably via aspartimide chemistry.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Department of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.
Spontaneous ionization/breakup of water at the surface of aqueous droplets has been reported with evidence ranging from formation of hydrogen peroxide and hydroxyl radicals, indicated by ions at m/z 36 attributed to OH⋅-HO or (HO-OH)⋅ as well as oxidation products of radical scavengers in mass spectra of water droplets formed by pneumatic nebulization. Here, aqueous droplets are formed both by nanoelectrospray, which produces highly charged nanodrops with initial diameters ~100 nm, and a vibrating mesh nebulizer, which produces 2-20 μm droplets that are initially less highly charged. The lifetimes of these droplets range from 10s of μs to 560 ms and the surface-to-volume ratios span ~100-fold range.
View Article and Find Full Text PDFJ Chem Phys
July 2024
Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
We applied reaction microscopy to elucidate fast non-adiabatic dissociation dynamics of deuterated water molecules after direct photo-double ionization at 61 eV with synchrotron radiation. For the very rare D+ + O+ + D breakup channel, the particle momenta, angular, and energy distributions of electrons and ions, measured in coincidence, reveal distinct electronic dication states and their dissociation pathways via spin-orbit coupling and charge transfer at crossings and seams on the potential energy surfaces. Notably, we could distinguish between direct and fast sequential dissociation scenarios.
View Article and Find Full Text PDFPhys Rev Lett
May 2024
Institute of Spectroscopy, Russian Academy of Sciences, 108840 Troitsk, Moscow, Russia.
We propose a simple dissipative system with purely cubic defocusing nonlinearity and nonuniform linear gain that can support stable localized dissipative vortex solitons with high topological charges without the utilization of competing nonlinearities and nonlinear gain or losses. Localization of such solitons is achieved due to an intriguing mechanism when defocusing nonlinearity stimulates energy flow from the ringlike region with linear gain to the periphery of the medium where energy is absorbed due to linear background losses. Vortex solitons bifurcate from linear gain-guided vortical modes with eigenvalues depending on topological charges that become purely real only at specific gain amplitudes.
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