Investigation of solvent microparticle formation in spray ionization–quadrupole ion trap–mass spectrometry

Abstract

AbstractIn the present study, a new method has been developed for the real‐time analysis of insource created solvent particles based on spray ionization–quadrupole ion trap–mass spectrometry (SI‐QIT‐MS). This is the first work in the literature reporting the formation of different solvent particles during solvent spray in mass spectrometry. The solvent particles formed from the solvent droplets are detected by a charge detector. Our ion trap system allows the measurement of a wide range particle masses. Various solvents and solvent mixtures such as water, methanol, acetone, toluene, n‐butanol, water‐methanol, and water‐ethanol were sprayed through a cone system, and the mass of the particles was monitored by different trap frequencies and voltages. While polar molecules produce larger and more diverse particles due to their strong intermolecular forces, apolar solvents generally do not produce a significant number of particles. We obtained results using a homemade ion trap mass spectrometer capable of determining the mass of micro‐sized solvent and solvent mixture particles weighing up to 1015 (Da). The instrument uses a charge detector connected to the exit of the ion trap. Simultaneous acquisition of particle mass spectra and measurement of the amount of charge in each particle allow mass assignment of each particle. Sprayed solvent particles were examined at various trap frequencies and voltages to find the best instrumental parameters for the highest trapping efficiency. The custom SI‐QIT‐MS instrument allows the measurement of the mass distribution of charged particles from the solvent spray.