Monitoring organic compounds in aqueous solution by rotating ball inlet mass spectrometry with continuous wave infrared laser desorption

Citation
En. Schmidt et al., Monitoring organic compounds in aqueous solution by rotating ball inlet mass spectrometry with continuous wave infrared laser desorption, SENS ACTU-B, 76(1-3), 2001, pp. 411-418
Citations number
14
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences","Instrumentation & Measurement
Journal title
SENSORS AND ACTUATORS B-CHEMICAL
ISSN journal
09254005 → ACNP
Volume
76
Issue
1-3
Year of publication
2001
Pages
411 - 418
Database
ISI
SICI code
0925-4005(20010601)76:1-3<411:MOCIAS>2.0.ZU;2-L
Abstract
The rotating ball inlet (ROBIN) is a mechanical device for introduction of a small stream of sample solution into a mass spectrometer or other systems by adherence of sample to the surface of a rotating ball. Using a simple q uadrupole mass spectrometer with an open ion source we have determined resp onse times and detection limits of ROBIN-MS for a variety of organic compou nds dissolved in water. The dependency of the detection limits on temperatu re and the effect of additional local heating of the vacuum exposed surface of the ball by continuous wave IR-laser were studied. The 0-90% response t ime for t-butanol and similar low molecular weight compounds with little af finity for binding to surfaces inside the vacuum system is about 0.5 s, in both rising and falling direction. With caffeine and similar compounds with significant affinity for binding to surfaces both the rising and the falli ng transient are biphasic with an initial rapid phase with a 0-90% response of about 0.5 s. The subsequent slow phase has a response time of several m inutes. Because of the wide separation of time scales of the fast and the s low response, the fast response can be used to quantify the analyte in flow injection analysis with a cycle time of 25 s. Detection limits for highly volatile organic compounds are unaffected by the temperature whereas detect ion limits for less volatile compounds decrease with increasing temperature . Compounds of low volatility can only be detected with IR-laser desorption . The lowest detection limits found are around 1 muM. Considerable improvem ent of the detection limits is expected with an optimal mass spectrometer. (C) 2001 Elsevier Science B.V. All rights reserved.