Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

TOF mass filter

FIGURE 3.7 Schematic of a lateral TOF mass filter. Ions enter the filter from the bottom left side, are displaced hy pulsed voltages on plates 1 and 4, and exit from the top-right sht. Reprinted with permission from Ref. [101]. American Institute of Physics. [Pg.42]

Magnetron Cluster Source with a Lateral TOF Mass Filter at the University of Birmingham... [Pg.47]

The cluster deposition apparatus at the group of Heinz Hovel uses a magnetron cluster source and a lateral TOF mass filter for cluster generation and mass selection. A cluster current of tens of pA is reported with a resolution greater than 50 for the lateral TOF mass filter. A cryopump is placed between the cluster source and mass... [Pg.59]

Figure 4.3 Simplified layouts of primary ion columns employing (a) Magnetic Sector filters, (b) Wien filters, and (c) Time Of Flight (TOF) mass filters. Operational aspects are discussed in the text. Additional lenses/deflectors/apertures are omitted for sake of clarity. Figure 4.3 Simplified layouts of primary ion columns employing (a) Magnetic Sector filters, (b) Wien filters, and (c) Time Of Flight (TOF) mass filters. Operational aspects are discussed in the text. Additional lenses/deflectors/apertures are omitted for sake of clarity.
The hexapole cannot act as a mass filter by applying a DC field and is used only in its all-RF mode, in which it allows all ions in a beam to pass through, whatever their m/z values. In doing so, the ion beam is constrained, so it leaves the hexapole as a narrow beam. This constraint is important because the ion beam from the inlet system tends to spread due to mutual ion repulsion and collision with residual air and solvent molecules. By injecting this divergent beam into a hexapole unit, it can be refocused. At the same time, vacuum pumps reduce the background pressure to about 10 mbar (Figure 22.1). The pressure needed in the TOF analyzer is about 10 ... [Pg.164]

B magnetic sector E = electric sector Q = quadrupole mass filter ToF = time-of-flight mass spectrometer IT = ion trap FTICR = Fourier-transform ion-cyclotron resonance. [Pg.386]

ToFs can also be used in combination with other mass analysers. Both hybrid sector and quadrupole systems are available. oaToF-MS has been interfaced to a quadrupole mass filter and hexapole gas collision cell, such as to allow recording of mass spectra and product ion spectra with good mass resolution (ca. 10000), high sensitivity, high mass range (ca. 10 000 Da) and high mass accuracy (<5ppm) [177,178]. QqToFMS may be fitted with API sources with flow-rates from nL... [Pg.392]

Undoubtedly, the technique most suited to tackle polyatomic multichannel reactions is the crossed molecular beam (CMB) scattering technique with mass spectrometric detection and time-of-flight (TOF) analysis. This technique, based on universal electron-impact (El) ionization coupled with a quadrupole mass filter for mass selection, has been central in the investigation of the dynamics of bimolecular reactions during the past 35 years.1,9-11 El ionization affords, in principle, a universal detection method for all possible reaction products of even a complex reaction exhibiting multiple reaction pathways. Although the technique is not usually able to provide state-resolved information, especially on a polyatomic... [Pg.331]

Different mass analysers can be combined with the electrospray ionization source to effect analysis. These include magnetic sector analysers, quadrupole filter (Q), quadrupole ion trap (QIT), time of flight (TOF), and more recently the Fourrier transform ion cyclotron resonance (FTICR) mass analysers. Tandem mass spectrometry can also be effected by combining one or more mass analysers in tandem, as in a triple quadrupole or a QTOF. The first analyzer is usually used as a mass filter to select parent ions that can be fragmented and analyzed by subsequent analysers. [Pg.237]

The concept of peak capacity is rather universal in instrumental analytical chemistry. For example, one can resolve components in time as in column chromatography or space, similar to the planar separation systems however, the concept transcends chromatography. Mass spectrometry, for example, a powerful detection method, which is often the detector of choice for complex samples after separation by chromatography, is a separation system itself. Mass spectrometry can separate samples in time when the mass filter is scanned, for example, when the mass-to-charge ratio is scanned in a quadrupole detector. The sample can also be separated in time with a time-of-flight (TOF) mass detector so that the arrival time is related to the mass-to-charge ratio. [Pg.16]

Orbital trapping mass spectrometers achieve resolutions of up to 105 and would be the next choice after ToF mass spectrometers if resolving powers above 104 are required. In addition to mass resolution, the selectivity of an MS can be critical to distinguish between co-eluting and not mass-resolved compounds. For example, typical triple-quad mass spectrometers usually cannot achieve better than unit-mass resolution. However, special operation modes like neutral loss scans and precursor ion scans can filter out compounds of interest even if neither LC separations nor MS scans would be sufficient to resolve these compounds (note that this is a filtering step). [Pg.117]

The compatibility is excellent with continuous ion sources such as ESI, dynamic SIMS, CF-FAB, ICP, El, Cl, etc. Sector instalments are not well-suited for pulsed ionization methods, although there are examples where MALDI sources have been utilized [225-229]. Sector instruments are usually larger and more expensive than other mass analyzers, such as TOFs, quadrupole filters, and traps. [Pg.49]

Like sector analyzers, quadrupole analyzers are well suited for continuous ion sources such as ESI, but are not well-suited for pulsed ionization methods. Quadmpole mass spectrometers are generally substantially cheaper and smaller than sector instruments and Qq-TOFs. They are very often used in combination with GC and LC, and single or triple quadmpole mass filters are very common benchtop instruments for routine measurements. [Pg.51]

Two types of mass analyzers have been used extensively in atmospheric applications quadrupole mass filters and time-of-flight (TOF) instruments. The use of ion traps is also being increasingly explored for this application. For the fundamental principles of mass... [Pg.564]

In this chapter we focus primarily on calibration of LC-MS where the mass spectrometer is operating at unit resolution, resolution that is sufficient to separate two peaks one mass unit apart. This kind of low-resolution mass filter covers almost 90 percent of the instruments commonly used for qualitative and/or quantitative analysis of small molecules. Batch-to-batch qualification testing of the instrument is also described. For the calibration of high-resolution mass spectrometers such as magnetic sector, TOF, or FTICR coupled with liquid chromatography, readers are referred to specific publications. [Pg.198]

The complications just described can be minimized if there is greater selectivity in the ionization process, as is sometime possible when photoionization is used as the excitation mechanism. Because the ionization energy can be more precisely controlled, it is possible in selected cases to produce only the desired reactant-ion species, or at least to minimize production of other ions. As already noted in the earlier section on formation of excited ions, it is also possible to populate specific internal-energy states of some reactant ions by using a photoionization source. One of the earliest photoionization mass spectrometers used to study interaction of internally excited ions with neutrals was that constructed by Chupka et al.91 Such apparatuses typically incorporate a photon source (either a line or a continuum source) and an optical monochromator, which are coupled to the reaction chamber. Various types of mass analyzer, including sector type, time-of-flight (TOF), and quadrupole mass filters, have been used with these apparatuses. Chupka has described the basic instrumental configuration in some detail.854 Photoionization mass spectrometers employed to study interactions of excited ions with neutral species have also been constructed in several other laboratories.80,1144,142,143 The apparatus recently developed by LeBreton et al.80 is illustrated schematically in Fig. 7 and is typical of such instrumentation. [Pg.115]

An intermediate resolution mass analyzer is the time of flight mass filter (TOF) [ 18,191- Applied to an ICP it allows resolutions below 1000 m/km. The... [Pg.1002]


See other pages where TOF mass filter is mentioned: [Pg.39]    [Pg.42]    [Pg.47]    [Pg.47]    [Pg.155]    [Pg.392]    [Pg.160]    [Pg.39]    [Pg.42]    [Pg.47]    [Pg.47]    [Pg.155]    [Pg.392]    [Pg.160]    [Pg.549]    [Pg.386]    [Pg.335]    [Pg.343]    [Pg.107]    [Pg.141]    [Pg.38]    [Pg.51]    [Pg.52]    [Pg.95]    [Pg.97]    [Pg.110]    [Pg.332]    [Pg.514]    [Pg.279]    [Pg.156]    [Pg.84]    [Pg.345]    [Pg.512]    [Pg.160]    [Pg.111]   
See also in sourсe #XX -- [ Pg.352 ]




SEARCH



Mass filter

© 2024 chempedia.info