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Thermospray technique, interfacing

The next major advance in LC-MS interfacing was developed by Blakely and Vestal (55, 56). To circumvent the solvent elimination problem, Blakely et al. (55) developed the thermospray interface that operates with aqueous-organic mobile phase at typical 4.6-mm i.d. column flow rates, 1-2 mL/min. The thermospray technique works well with aqueous buffers. This feature is an advantage when the versatility of the reversed-phase mode is considered. In fact, with aqueous buffers, ions are produced when the filament is off. A recent improvement in the thermospray technique is the development of an electrically heated vaporizer that permits precise control of the vaporization (56). This... [Pg.135]

An ideal interface should not cause extra-column peak broadening. Historical interfaces include the moving belt and the thermospray. Common interfaces are electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCl). Several special interfaces include the particle beam—a pioneering technique that is still used because it is the only one that can provide electron ionization mass spectra. Others are continuous fiow fast atom bombardment (CF-FAB), atmospheric pressure photon ionization (APPI), and matrix-assisted laser desorption ionization (M ALDl). The two most common interfaces, ESI and APCI, were discovered in the late 1980s and involve an atmospheric pressure ionization (API) step. Both are soft ionization techniques that cause little or no fragmentation hence a fingerprint for qualitative identification is usually not apparent. [Pg.147]

Three LC-MS interfacing techniques were compared. When using the thermospray (TSP) interface, [M — H] or [M - - CHsCOO]" were obtained as the main ions. APCI and ion spray (ISP) interfaces gave [M — H] at 20-30 V as the main ion. Calibration graphs were linear from 1 to 100 ng for each compound with repeatability values of 15-20%. Instrumental LOD for APCI were 3-180 ng in full scan and from 0.001-0.085 ng in SIM mode. Instrumental LOD for ISP and TSP were larger by approximately one order of magnitude . [Pg.955]

Particle beam LC-MS is a rapidly developing complimentary interface to thermospray techniques and provides a method of linking conventional HPLC systems with eluant flow-rates of 0.3-1.0mlmin , to an El ion source to obtain the classical El spectra which can be compared to conventional reference spectra (Figure 7.12). A capillary GC column may be connected to the same interface [10]. LC eluant enters the interface together with a stream of helium to form an aerosol of droplets which move through the desolvation chamber maintained at room temperature and pressure. The... [Pg.383]

Thermospray interface. Provides liquid chromatographic effluent continuously through a heated capillary vaporizer tube to the mass spectrometer. Solvent molecules evaporate away from the partially vaporized liquid, and analyte ions are transmitted to the mass spectrometer s ion optics. The ionization technique must be specified, e.g., preexisting ions, salt buffer, filament, or electrical discharge. [Pg.433]

In summary, it can be said that prior to the development of the thermospray interface there were an increasing nnmber of reports of the analytical application of LC-MS [3] bnt in this present anthor s opinion, based on a nnmber of years of using a moving-belt interface, the technique could not be considered to be routine . The thermospray interface changed this and with the commercial intro-dnction of the combined APCI/electrospray systems in the 1990s the technique, for it now may be considered as a true hybrid technique, has reached maturity (although this should not be taken as a suggestion that there will be no further developments). [Pg.135]

Examples of such compounds include anionic surfactants whose analysis had previously been limited to desorption techniques such as FAB and thermospray but which yielded interpretable El spectra when using a parUcle-beam interface... [Pg.149]

The introduction of the thermospray interface provided an easy-to-use LC-MS interface and was the first step in the acceptance of LC-MS as a routine analytical technique. It soon became the most widely used LC-MS interface of those available in the mid to late 1980s. [Pg.155]

Electrospray ionization occurs by the same four steps as listed above for thermospray (see Section 4.6). In contrast to thermospray, and most other ionization methods nsed in mass spectrometry, it shonld be noted that electrospray ionization nnnsnally takes place at atmospheric pressure. A similar process carried out under vacuum is known as electrohydrodynamic ionization and gives rise to qnite different analytical results. This technique has not been developed into a commercial LC-MS interface and will not be considered further. [Pg.158]

Thermospray was quite popular before the advent of electrospray, but has now given way to the more robust API techniques, although TSP sources continue to operate. Developed as an LC-MS interface, this technique calls for a continuous flow of sample in solution. [Pg.377]

A group of techniques employing differential selection of solute ions relies on nebulisation and ionisation of the eluent, with some discrimination of ion selection in favour of the solute. Main representatives are APCI [544] and thermospray [545]. In a thermospray interface a supersonic jet of vapour and small droplets is generated out of a heated vaporiser tube. Controlled, partial vaporisation of the HPLC solvent occurs before it enters the ion source. Ionisation of nonvolatile analytes takes place by means of solvent-mediated Cl reactions and ion evaporation processes. Most thermospray sources are fitted with a discharge electrode. When this is used, the technique is called plasmaspray (PSP) or discharge-assisted thermospray. In practice, many... [Pg.505]

These problems have largely been solved by the development of a wide variety of powerful LC-MS interfaces (reviewed in Refs. [1-3]). In the following paragraphs, the two most widely used atmospheric pressure ionisation (API) systems, namely atmospheric pressure chemical ionisation (APCI) and electrospray ionisation (ESI), are briefly described, along with the older technique of thermospray ionisation... [Pg.144]

The two most common LG/MS interfaces used for routine quantitative analyses are APCI and APT electrospray. The principles of these techniques in direct infusion analyses have been described earlier (see Sections 3.3 and 3.4). As APTelectrospray has a broader application profile, its use is more widespread than APCI. Other configurations including El, atmospheric pressure photoionization (APPl), and thermospray interfaces with liquid chromatographs are available but are less commonly used for high throughput or routine analysis. [Pg.162]

Most of the direct and indirect (transport) interfaces described here use chemical ionization (c.i.) ion-sources, which are not well suited to such polar, non-volatile compounds as tri- and higher oligosaccharides. The thermospray interface, which can operate on an ion-evaporative mode, is capable of producing intact molecular ions from such nonvolatile, polar molecules and should be useful in oligosaccharide analysis. Molecules of this type, however, can also be easily analyzed by fast-atom-bombardment ionization, and use of this technique, coupled to direct liquid introduction and moving-belt interfaces, has been reported. The latter system has been applied to complex oligosaccharide analysis. ... [Pg.70]

Confirmation by LC-MS This method is not used much, since it involves expensive apparatus, and rather good experience in the technique is needed. Abramson (66) illustrated the advantages resulting from the combination of liquid chromatography and mass spectrometry for ochratoxin A in barley. Among the types of interfaces most used for ochratoxin A analysis were thermospray, direct liquid induction (DLI), and... [Pg.509]


See other pages where Thermospray technique, interfacing is mentioned: [Pg.403]    [Pg.378]    [Pg.748]    [Pg.85]    [Pg.84]    [Pg.403]    [Pg.36]    [Pg.211]    [Pg.209]    [Pg.327]    [Pg.546]    [Pg.403]    [Pg.246]    [Pg.142]    [Pg.183]    [Pg.285]    [Pg.504]    [Pg.506]    [Pg.510]    [Pg.26]    [Pg.375]    [Pg.379]    [Pg.719]    [Pg.84]    [Pg.125]    [Pg.545]    [Pg.20]    [Pg.377]    [Pg.1325]    [Pg.959]   


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