Fourier transform mass analyser

Table 6.33 Main characteristics of Fourier-transform mass analysers...

Along with advances in various ionization sources, significant improvements have been made in the area of mass analyzers. Mass analyzers can be differentiated based on several attributes such as scan speed, duty cycle, mass resolution, mass range, and cost [126], The most common analyzers used for metabonomics analyses include the quadrupole and TOF-based analyzers [125-127], Some other analyzers that have been reported for use in MS-based metabonomics analyses are the ion traps, Orbitraps, and Fourier transform mass spectrometers [128,129],... 

Fourier transform mass spectrometry was devised by Comisarow and Marshall in 1974 at the University of British Columbia. This method uses Fourier transformation, which is a mathematical way to convert a set of data involving a time domain into a set of frequencies. The mathematical concept of Fourier transformation is important and has been used in analyses of the protein structure by mass spectrometry, X-ray crystallography, and nuclear magnetic resonance (NMR). 

Further performance improvements in analysing nucleic acids could be achieved by the introduction of 3-hydroxypicolinic add as matrix [8] and the introduction of delayed extraction in a linear time-of-flight mass spectrometer [9]. If, for MALDI Fourier transform mass spectrometry, the molecular weight range in analysing nucleic add fragments could be extended further this type of MALDI MS would become of significant value due to the extraordinary resolution possible [10, 11]. In order to reach the sensitivity level necessary for MALDI-TOF MS analysis an amplification step has to be incorporated into the sample preparation process for... 

Analyses were performed using a modified laser microprobe Fourier transform mass spectrometer (FTMS). This instrument is differentially pumped with a dual-cell Nicolet Instrument FTMS 2000 (Thermoquest, Madison,... 

A new method was developed for the separation of three known and ten new anthraquinone pigments. In addition, five new pigments were determined by fourier transformation mass spectrometric detection (FTMS) as co-eluting impurities (120). The analyses were performed on a Kinetex C18 column. 

In mass spectrometers, ions are analysed according to the ml7. (mass-to-charge) value and not to the mass. While there are many possible combinations of technologies associated with a mass-spectrometry experiment, relatively few forms of mass analysis predominate. They include linear multipoles, such as the quadrupole mass filter, time-of-flight mass spectrometry, ion trapping forms of mass spectrometry, including the quadrupole ion trap and Fourier-transform ion-cyclotron resonance, and sector mass spectrometry. Hybrid instruments intend to combine the strengths of the component analysers. 

In analyses where molecular masses are being matched, more accurate mass measurements provide more reliable matches and identifications.26,65,66 In a reference laboratory the mass accuracy to several decimal points, provided by a Fourier transform ion cyclotron resonance mass analyzer, may be desirable. In field or portable systems there is usually a trade-off in mass accuracy for size and ruggedness. Reliable identifications can be made with moderate mass accuracy, even 1 Da, if a large enough suite of molecular ions is recorded and used to search the database. If both positive ion and negative ion spectra are... 

In addition to the diversity of ionisation techniques available, mass spectrometers offer a selection of mass analyser configurations. Of note are single (MS) and triple quadrupole (MS—MS) instruments, ion trap analysers (MS)n, time-of-flight (ToF) analysers, sector field analysers, and Fourier transform-ion cyclotron resonance (FTICR) instruments. 

Numerous analyses in the quality control of most kinds of samples occurring in the flavour industry are done by different chromatographic procedures, for example gas chromatography (GC), high-pressure liquid chromatography (fiPLC) and capillary electrophoresis (CE). Besides the different IR methods mentioned already, further spectroscopic techniques are used, for example nuclear magnetic resonance, ultraviolet spectroscopy, mass spectroscopy (MS) and atomic absorption spectroscopy. In addition, also in quality control modern coupled techniques like GC-MS, GC-Fourier transform IR spectroscopy, HPLC-MS and CE-MS are gaining more and more importance. 

One of the principal contributions of electronic data processing over the past several years in terms of chemical analysis is the saving of manual effort in interpreting analytical data. Special techniques, such as Fourier transform, have increased speed (as well as sensitivity) by orders of magnitude in connection with infrared, nuclear magnetic resonance, and mass spectroscopy, Of course, for on-line process analyses, essentially instantaneous interpretation is required to provide the proper error signal that is used to position the final control element (valve, feeder, damper, etc.). 

To shed light on the mechanism of formation of silsesquioxane a7b3, to identify the species formed during the process, and to try to explain the high selectivity towards structure a7b3 of the optimised synthetic method described above (64% yield in 18 h), the synthesis of cyclopentyl silsesquioxane a7b3 was monitored by electrospray ionisation mass spectrometry (ESI MS) [50-52] and in situ attenuated total reflection Fourier-transform infrared (ATR FTIR) spectroscopy [53, 54]. Spectroscopic data from the latter were analysed using chemometric methods to identify the pure component spectra and relative concentration profiles. 

However, most modem highly accurate time-of-flight (TOF), Fourier-transform ion cyclotron resonance (FT-ICR) and Orbitrap mass analysers [107] have not been reported for TA analysis so far and are thus not discussed in this chapter. 

The orbitrap is an electrostatic ion trap that uses the Fourier transform to obtain mass spectra. This analyser is based on a completely new concept, proposed by Makarov and described in patents in 1996 [26] and 2004 [27], and in Analytical Chemistry in 2000 [28], A third patent describes a complete instrument including an atmospheric pressure source [29], Another article was also published with Cooks in 2005 [30]. The first commercial instrument was introduced on the market by the Thermo Electron Corporation in June 2005. 

Orbitrap analyser a mass analyser that store the ions in a quadro-logarithmic field. The ions are selectively detected according to their m/z values using their induced current. The treatment of this current by a Fourier transform yields their mass-to-charge ratios. It is an analyser with very high-resolution capacity. 

Analysis of trace compounds. All fractions were checked by capillary gas chromatography (GC) with FID and sulfiir specific detection (flame photometric detector, FPD ThermoQuest CE, Egelsbach). Subsequently the different fractions were analyzed by capillary gas chromatography-mass spectrometry (GC-MS). Specific unknowns were enriched by preparative multidimensional gas chromatography (MDGC). For further structure elucidation complementary analyses using GC-MS and capillary gas chromatography-Fourier transform infrared spectroscopy (GC-FTIR) as well as H-NMR were applied. All new compounds have been synthesized and characterized by GC-olfactometry (GC-0). 

---