Probing electrically driven nanojets by energy and mass analysis in vacuo

Time of flight (TOF) and energy analysis in vacuum are used in series to determine jet velocity Uj, diameter dj, electrical potential Vj and energy dissipated ΔV at the breakup point of electrified nanojets of the ionic liquid 1-Ethyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate (EMI-FAP) (Ignat'ev et al., J. Fluorine Chem., vol. 126, issue 8, 2008, pp.1150–1159). The full spray is periodically gated by a grid held at a high voltage Vg, and received at a collector where the measured flight times provide the distribution of drop speeds u. Varying Vg provides the bivariate distribution of drop energies ξ and velocities. The collector plate, centred with the beam axis, is divided into eight concentric rings, yielding the angular distribution of the spray current, and high resolution (u,ξ) values in the whole spray. The energies of various particles of given u are all well defined, but depend uniquely on u, even though u and ξ are in principle independent experimental variables. Slow and fast particles have energies respectively well above and below the capillary voltage Ve (1.64 kV). As previously shown by Gamero-Castaño & Hruby (J. Fluid Mech., vol. 459, 2002, pp. 245–276), this behaviour is due to the 2-stage acceleration process, first jointly in the jet for all particles, and then separately for free flying drops or ions of different mass/charge. The measured two-dimensional distributions of u and ξ provide the jet velocity Uj (~0.44 km s−1) and electrical potential Vj (1.2 kV) at the breakup point. All molecular ions originate near the breakup point rather than the meniscus neck. A measurable fraction of anomalously fast drops is observed that must come from Coulomb fissions of the main drops.

The Elevation of LC-ESI-Q-TOF-MS Response in the Analysis of Isoquinoline Alkaloids from Some Papaveraceae and Berberidaceae Representatives

Twenty-five methanol extracts obtained from various representatives of Papaveraceae and Berberidaceae botanical families (genera: Papaver, Argemone, Eschscholzia, Chelidonium, Glaucium, and Berberis) were screened for their alkaloid content in an optimized method suitable for the LC-ESI-Q-TOF-MS analysis. Twelve pharmacologically important isoquinoline alkaloids from four groups, aporphines, benzylisoquinolines, protoberberines, and benzophenanthridines, present in these traditionally used plant species were quantitatively determined in each studied sample, providing their alkaloid profile. A Zorbax Stable Bond RP-18 column and a mobile phase composed of 0.1% formic acid and 0.1% formic acid in acetonitrile (v/v) were used at the flow rate of 0.2 mL/min. A profound study on the optimization of MS response to four groups of isoquinoline alkaloids (validation of capillary voltage, gas flows, nebulizer pressure, skimmer, and fragmentor voltages), repeatability of results, and stability and linearity of measurements were described, showing, among others, 3000 V of capillary voltage, 350°C of gas temperature, 12 L/min of gas flows, nebulizer pressure of 35 psig, 65 V for skimmer voltage, and 30 V for collision energy as the most advantageous operation parameters.

A study on electrospray mass spectrometry of fullerenol C60(OH)24

Full characterization of fullerenol C60(OH)24 by HPLC ESI-MS in negative and positive ionization modes was achieved. Fragmentor voltage and capillary voltage were optimized in order to obtain a good signal stability and the best peak intensity distribution for the fullerenol C60(OH)24 in both negative and positive modes. While the predominant base peak observed for C60(OH)24 in the negative ionization mode was [M − H]− at m/z 1127, those observed in the positive mode were multiply charged [M − H2O + 4H]4+ at m/z 279 and [M − 12H2O + 2NH3 + 6H]6+ at m/z 158.