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Liquid direct introduction

Direct liquid introduction interface. An interface that continuously passes all, or a part of, the effluent from a liquid chromatograph to the mass spectrometer the solvent usually functions as a chemical ionization agent for ionization of the solute. [Pg.432]

Seven different LC-MS interfaces are described in Chapter 4, with particular emphasis being placed on their advantages and disadvantages and the ways in which the interface overcomes (or fails to overcome) the incompatibilities of the two techniques. The earlier interfaces are included for historical reasons only as, for example, the moving-belt and direct-liquid-introduction interfaces, are not currently in routine use. The final chapter (Chapter 5) is devoted to a number of illustrative examples of the way in which LC-MS has been used to solve various analytical problems. [Pg.11]

El may be used with the moving-belt and particle-beam interfaces. Cl with the moving-belt, particle-beam and direct-liquid-introduction interfaces, and FAB with the continuous-flow FAB interface. A brief description of these ionization methods will be provided here but for further details the book by Ashcroft [8] is recommended. [Pg.52]

The direct-liquid-introduction (DLI) interface was made available commercially just after the moving-belt interface to which, as no company produced both types, it was an alternative. At this time, therefore, the commercial LC-MS interface used within a laboratory was dictated by the manufacturer of the mass spectrometer already in use unless a new instrument was being purchased solely for LC-MS applications. The development of LC-MS in the early 1980s was such that this was very rare and it was therefore unusual that a scientific evaluation was carried out to assess the ability of a type of interface to solve problems within a particular laboratory. [Pg.140]

The direct-liquid-introduction interface is shown schematically in Figure 4.2. This system is effectively a probe, at the end of which is a pinhole of approximately 5 p.m diameter, which abuts a desolvation chamber attached to the ion source of the mass spectrometer. The eluate from an HPLC column is circulated... [Pg.140]

Figure 4.2 Schematic of a direct-liquid-introduction LC-MS interface. From applications literature published by Agilent Technologies UK Limited, Stockport, UK, and reproduced with permission. Figure 4.2 Schematic of a direct-liquid-introduction LC-MS interface. From applications literature published by Agilent Technologies UK Limited, Stockport, UK, and reproduced with permission.
Moving wire/belt Direct liquid introduction Thermospray Particle beam... [Pg.765]

LC-MS inlet probes support all conventional HPLC column diameters from mobile phase must be eliminated, either before entering or from inside the mass spectrometer, so that the production of ions is not adversely affected. The problem of removing the solvent is usually overcome by direct-liquid-introduction (DLI), mechanical transport devices, or particle beam (PB) interfaces. The main disadvantages of transport devices are that column... [Pg.499]

In reduced-flow LC-MS systems, the solvent flow into the spectrometer is reduced to a level where the pumping system can cope. Essentially, three such systems have been developed direct-liquid-introduction (DLI), flowing FAB [531] and electrospray [532]. An alternative approach to belt transport interfacing is to deliver the column eluate directly into the MS source and use Cl techniques. Methods based on this principle are called direct-liquid-injection systems, which are comprised of capillary flow restrictors, diaphragms,... [Pg.503]

DLI (1) Direct laser ionisation (2) Direct liquid introduction (3) Direct liquid interface... [Pg.752]

J.D. Henion, A comparison of direct liquid introduction LC/MS techniques employing microbore and conventional packed columns, J. Chromatogr. Sci., 18 (1980) 101-115. [Pg.398]

Direct liquid introduction (DLI) is the simplest and most straightforward approach. It was first attempted and reported by Tal Rose et al. [Pg.717]

The thermospray interface overcame many of the problems encountered with the moving-belt and direct-liquid-introduction interfaces and with the advent of this, LC-MS became a routine analytical tool in a large number of laboratories. This was reflected in the fact that this was the first type of interface made available commercially by the majority of the manufacturers of mass spectrometers. [Pg.94]

Many interfaces have been developed to meet these demanding challenges. Some of these coupling methods, such as the moving belt or the particle beam interface, are based on the concomitant elimination of the solvent before it enters the mass spectrometer. Other methods such as direct liquid introduction (DLI) or continuous flow FAB rely on splitting the flow of the liquid that is introduced into the interface in order to obtain a flow that can be directly infused into the ionization source. However, these types of interfaces can only handle a fraction of the liquid flow from the LC. [Pg.506]

An alternative to direct liquid introduction is the moving belt, or moving-wire, transport interface. Because all l.c. solvents are evaporated before the sample is transported into the ion source, fewer restrictions are placed on solvent type, flow rates, or buffer composition. This system has been used for analysis of mixtures of pentoses, hexoses, and disaccha-rides. ... [Pg.70]

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]

The first approaches to the coupling of liquid-phase separation techniques with mass spectrometry were designed for HPLC needs, starting in the 1970s with since-forgotten techniques such as direct liquid introduction (DLI) and moving belt. In the 1980s, techniques such as thermospray, continuous-flow-fast atom bombardment (CF-FAB), and particle beam arose. [Pg.338]


See other pages where Liquid direct introduction is mentioned: [Pg.6]    [Pg.14]    [Pg.138]    [Pg.140]    [Pg.401]    [Pg.489]    [Pg.997]    [Pg.375]    [Pg.376]    [Pg.376]    [Pg.717]    [Pg.77]    [Pg.80]    [Pg.82]    [Pg.293]    [Pg.508]    [Pg.69]    [Pg.377]    [Pg.377]   
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