Patent Application
20050255603
The present invention relates to a method for detecting any of a number of substances present in gases or gas mixtures containing alkanes, ethane or ethyne, using chemical ionization mass spectrometry.
Chemical ionization mass spectrometry has been used for analyte identification since the development of mass spectrometry [Munson, M. S. B.; Fjeld, F. H. J. Amer. Chem. Soc., 88, 2621-2630 (1966); Munson, M. S. B.; Field, F. H. J. Amer. Chem. Soc., 88, 337-4345, (1966); Munson, M. S. B.; Field, F. H. J. Amer. Chem. Soc., 89, 1047-1052, (1967)]. In recent years instruments utilizing chemical ionization sources have been marketed for analysis of gas mixtures [Linforth, R.; Preece, S. Technical Note 236, Micromass Ltd, (1998); Adechy, M.; Shress, V.; Squibb, A. Peak, 1, 2-4, (2000)]. The combination of a chemical ionization source with flow tube reactor techniques allows both identification and quantification of trace species without internal calibration. Two closely related systems have been developed using this combination of techniques; Proton Transfer Mass Spectrometry [Lindinger, W.; Hansel, A.; Jordan, A. Int. J. Mass Spectrom; Jon Proc., 173, 191-241, {1998)] and Selected Ion Flow Tube Mass Spectrometry [Spanel, P.; Smith, D. Mea Bioi. Eng. Comput., 34, 409-419, (1996)].
The selection of the chemical ionizing agent or precursor ion is critical to the application of the technique. The precursor ion must be reactive with the analyte molecule(s) but unreactive with the bulk gas within which the analyte is present as a trace component. In most applications to date the bulk gas is ambient air or exhaled breath and the analyte species are various Volatile Organic Compounds (VOCs).
Precursor ions which have been in common use include NO+, O2+, NH4+ and OH− A further important criterion for selection of a chemical ionization precursor is the facility with which it can be generated in large amounts using typical instrumentation such as an electron impact or microwave discharge source.
It is known from previous experimental work (Freitas, M. A. O'Hair, R. A. J. Int. J. Mass Spectrom; Ion Proc 1998, 175, 102-122) that the methoxymethyl cation is not reactive with alkanes but will react with molecules containing heteroatoms. However, the use of CH3OCH2+ as a chemical ionization reagent for quantification and identification of analytes has not been tried previously.
In one form the invention is a method of detecting and quantifying trace levels of molecules containing one or more of a range of reactive species, in gases or gas mixtures consisting of alkanes, ethene, or ethyne, said method including using an alkoxyalkyl cation as the chemical ionisation precursor in a selected ion flow tube mass spectrometer.
Preferably the method further includes reacting the sample gas to be analysed with the alkoxyalkyl cation in a stream of helium in the flow tube.
Preferably the alkoxyalkyl cation is a methoxymethyl cation.
The invention in another aspect comprises a method of detecting and quantifying a gas sample containing trace levels of molecules containing one or more of a range of reactive species, in gases or gas mixtures consisting of alkanes, ethene, or ethyne in a selected ion flow tube mass spectrometer comprising the steps of:
producing a supply of alkyoxymethyl cations,
mass electing the alkyoxymethyl cations,
inducing a flow of the alkyoxymethyl cations into the inlet of a flow tube of the spectrometer in a carrier flow of helium
reacting the gas sample with the alkyoxymethyl cations,
analysing the reacted gas sample in the mass spectrometer, and
calculating the concentration of the trace levels of molecules containing heteroatoms present in the reacted gas sample.
Preferably the alkyoxymethyl cation is a methoxymethyl cation.
Preferably the range of reactive species includes molecules that contain sulphur, nitrogen, oxygen, phosphorus or silicon heteroatoms,
By way of example only, a preferred embodiment of the present invention is described in detail with reference to the accompanying flow chart.
Referring to the flow chart, in step 1, a supply of methoxymethyl cations is produced. This may be done by any of a number of known methods, for example, using the helium flowing afterglow method in which a stream of helium gas is passed in a pyrex or quartz tube through a microwave discharge and a small amount of dimethoxymethane is added to the gas stream emerging from the tube. Methoxymethyl cations are produced by a reaction between the helium metastable species and the dimethoxymethane.
Another process which may be used to produce the methoxymethyl cations is electron impact using an incandescent rhenium filament within a vacuum chamber filled with a low pressure dimethoxymethane.
In step 2, the methoxymethyl cations are mass selected, using a mass spectrometer.
In step 3, the methoxymethyl cations are introduced into the inlet of a flow tube in a carrier flow of helium, at ambient temperature and at a pressure of about 0.5 Torr.
As the mixture of helium and methoxymethyl cations flow along the flow tube, the sample gas to be analysed is introduced into the flow tube via a capillary inlet (step 4).
In step 5, the methoxymethyl cations react with the gas sample, which is primarily one or more alkane gases, but which also contains traces of molecules containing heteroatoms, (e.g. sulphur, nitrogen). This type of gas sample is typical of the type of sample from a leaking gas pipe.
The methoxymethyl [CH3OCH2+] ion is unreactive with alkanes, ethene and ethyne, i.e. the hydrocarbons that are present as bulk constituents of natural gas and other hydrocarbon fuel mixtures viz methane, CH4; ethane, C2H6; propane, C3H8; butane, C4H10; ethylene, C2H4 and acetylene, C2H2. The CH3OCH2 ion is, however, reactive with many sulfur-containing and nitrogen-containing species, including methanethiol, CH3SH; ethanethiol, C2H5SH; dimethylsulfide, (CH3)2S and diethylsulfide, (C2H5)2S.
The reactivity of CH3OCH2+ with selected neutral species in a pressure of 0.5 Torr of helium at room temperature is shown in Table 1.
The reacted gas sample produced in step 5 is then analysed in known manner in a mass spectrometer (step 6). Since the methoxymethyl cations react only with the molecules containing the heteroatoms, analysis of the mass spectrometry results can be used to calculate the concentration of the trace species containing heteroatoms present in the alkane gases.
Although the preferred alkoxyalkyl cation is highly preferred, other oxy-radicals can also be employed. For example, but without limiting suitable oxy-radicals are peroxynitrite, alkoxy cations and reactive oxygen species such as HOCl can be employed with appropriate substrates.
One application of the method herein described is to enable leaks of gas from gas lines or gas containers to be easily and simply detected. Producers of gas often add substances containing sulphur or other odiferous material to gas to aid the detection of leaks, and it is very useful to be able to detect small leaks by detecting the very small quantities of the sulphur-containing or other added material. For this, it is necessary to have a detection method which reacts with the sulphur-containing or other added material but does not react with the bulk gas or with the major constituents of air,
It will be appreciated that the detection of leaks from has lines is only one of many applications resulting from the present invention and the method of the present invention has an application in many other fields.
Because the method as herein described uses SIFT-MS technology, it is possible to identify and quantify the reaction product, ethylene, of the methoxymethyl radical reaction with the substrate. In addition it is possible to carry out the identification and quantification in ‘real time’ and so can be used to characterise the kinetics of the oxyradical-substrate interaction. Consequently it is possible to make quantitive and kinetic comparisons between different reaction mixtures.
Having disclosed preferred forms of the invention, it will be apparent to those skilled in this particular art that modifications and changes can be made to various parameters and yet still come within the general concept of the invention. All such modifications and changes are intended to be included in the scope of the invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 520070 | Jul 2002 | NZ | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/NZ03/00145 | 7/8/2003 | WO | 6/15/2005 |
