THIN PERVAPORATION MEMBRANES FOR IMPROVED PERFORMANCE IN ONLINE FLOW-INJECTION ANALYSIS MEMBRANE INTRODUCTION MASS-SPECTROMETRY

Citation
N. Kasthurikrishnan et al., THIN PERVAPORATION MEMBRANES FOR IMPROVED PERFORMANCE IN ONLINE FLOW-INJECTION ANALYSIS MEMBRANE INTRODUCTION MASS-SPECTROMETRY, Rapid communications in mass spectrometry, 10(7), 1996, pp. 751-756
Citations number
35
Categorie Soggetti
Spectroscopy,"Chemistry Analytical
ISSN journal
09514198
Volume
10
Issue
7
Year of publication
1996
Pages
751 - 756
Database
ISI
SICI code
0951-4198(1996)10:7<751:TPMFIP>2.0.ZU;2-0
Abstract
Characterization of some thin (10-50 mu m) and selective (zeolite fill ed) sheet pervaporation membrane materials for the on-line analysis of volatile compounds in solution by membrane introduction mass spectrom etry and dow injection analysis is reported, A comparison of the membr ane performance, both in aqueous (normal) and organic (reverse) phase, is made using a seven-component test mixture and a triple quadrupole mass spectrometer, While no significant difference is observed in the normal phase experiments, reverse phase experiments with the thin memb ranes showed an improvement in rise times and analysis times by a fact or of two, Thus, the thin membranes are more suitable for chemical and petrochemical on-line process monitoring where the frequency of sampl ing is of great importance, The thin hydrophobic membranes allow enoug h water to permeate the membrane for chemical ionization to be perform ed as an alternative to electron impact provided an ion trap mass spec trometer is used. The detection limits observed for the compounds stud ied using water as a chemical ionization reagent are similar to those achieved by a two-stage enrichment microporous membrane/jet separator device interfaced to an ion trap mass spectrometer and are in the lowe r parts-per-billion range for some of the compounds studied (5 ppb for methyl ethyl ketone, 5 ppb for acetone), Thus the thinner hydrophobic membranes offer the unique combination of rapid permeation and low de tection limits in chemical ionization experiments with an ion trap.