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Quadrupole array

Once the ions have been focussed through the orifice and into the analyser portion they are further focussed by electrostatic lenses into the first of three axially aligned quadrupole arrays. The first and third arrays can be operated as mass filters while the central quad (Q2 in Figure 1) functions only as an ion guide, incapable of resolving one mass from another. [Pg.78]

Xia, Y. Thomson, B.A. McLuckey, S.A. Bi-directional ion transfer between quadrupole arrays MS" ion/ion reaction experiments on a quadrupole/time-of-flight tandem mass spectrometer. Anal. Chem. 2007, 79, 8199-8206. [Pg.29]

Flow injection Chemical ionisation (Cl) Quadrupole ion trap (QITMS) Diode array detector... [Pg.352]

FTIR in multiply hyphenated systems may be either off-line (with on-line collection of peaks) [666,667] or directly on-line [668,669]. Off-line techniques may be essential for minor components in a mixture, where long analysis times are required for FT-based techniques (NMR, IR), or where careful optimisation of the response is needed. In an early study a prototype configuration comprised SEC, a triple quadrupole mass spectrometer, off-line evaporative FTIR with splitting after UV detection see Scheme 7.12c [667]. Off-line IR spectroscopy (LC Transform ) provides good-quality spectra with no interferences from the mobile phase and the potential for very high sensitivity. Advanced approaches consist of an HPLC system incorporating a UV diode array, FTIR (using an ATR flow-cell to obtain on-flow IR spectra), NMR and ToF-MS. [Pg.524]

Multiple mass analyzers exist that can perform tandem mass spectrometry. Some use a tandem-in-space configuration, such as the triple quadrupole mass analyzers illustrated (Fig.3.9). Others use a tandem-in-time configuration and include instruments such as ion-traps (ITMS) and Fourier transform ion cyclotron resonance mass spectrometry (FTICRMS or FTMS). A triple quadrupole mass spectrometer can only perform the tandem process once for an isolated precursor ion (e.g., MS/MS), but trapping or tandem-in-time instruments can perform repetitive tandem mass spectrometry (MS ), thus adding n 1 degrees of structural characterization and elucidation. When an ion-trap is combined with HPLC and photodiode array detection, the net result is a profiling tool that is a powerful tool for both metabolite profiling and metabolite identification. [Pg.47]

C. Baiocchi, M.C. Brussino, E. Pramauro, A.B. Prevot, L. Palmisano and G. Marci, Charac-terizaton of methyl orange and its photocatalytic degradation products by HPLC/UV-VIS diode array and atmospheric pressure ionization quadrupole ion trap mass spectrometry. Int. J. Mass Spectr., 214 (2002) 247-256. [Pg.568]

The resolution of an FPD is theoretically limited by the number of channels (512-2048). In practice, it is even less because the image suffers some broadening as it passes from the first MCP to the photodiode array (Fig. 4.63). Therefore, instruments with FPD can normally be switched from FPD to SEM detection, e.g., by vertical electrostatic deflection of the ion beam (Finnigan MAT900). Furthermore, quadrupole lenses or an inhomogeneous ESA behind the magnet are employed to achieve variable dispersion, i.e., to zoom the m/z range of simultaneous... [Pg.179]

Recently, comparatively inexpensive, very reliable, and stable single quadrupole mass spectrometers have entered the market. These spectrometers can be coupled to GC, LC, and CE separation methods simply by modifying the sampling interfaces. Although these detectors are more expensive than most conventional detectors including the versatile electron capture and diode array absorbance detectors used for GC and LG respectively, the reduction in sample preparation effort and their increased specificity can often rapidly... [Pg.156]

Reverse-phase columns with a gradient elution in combination with UV-Vis spectrophotometers using photodiode-array (PDA) (Fig. 1.6) and spectrofiuorimeters are common devices employed in this technique. In a lesser extent, MS, tandem mass spectrometry (MS-MS), and nano liquid chromatography-electrospray ionization-quadrupole time-of-flight tandem mass spectrometry (nanoLC-nanoESI-Q-qTOF-MS-MS) has been used as detection system. This instrumentation has been mainly used in the analysis of dyes and proteinaceous media, and in some extent, in the analysis of drying oils and terpenoid varnishes [47,48],... [Pg.22]

In this expansion the dipole-dipole term is the most prominent if donor-acceptor distance R is not too small. The dipole-dipole term represents the interaction between the transition dipole moments Md and MA of donor and acceptor molecules, respectively. The square of these transition dipoles is proportional to the oscillator strengths fy> and fA for radiative transitions in the individual donor and acceptor molecules (equation 3.73). Higher order terms such as electric dipole-electric quadrupole, electric-dipole-magnetic dipole, become important at close approach and may be effective in crystals and highly ordered array of chromophores. [Pg.192]

Detector The detector is the last major portion of the mass spectrometer, and it detects the presence, and preferably abundance, of ions after they have exited the mass analyzer. Examples include the electron multiplier, common on quadrupole instruments, and the microchannel plate (an array of electron multipliers), which have been common on TOF instruments. For most users, the actual detector is a relatively invisible portion of the instrument that needs little or no regular attention. [Pg.20]

Martens-Lobenhoffer et al. [119] used chiral HPLC-atmospheric pressure photoionization tandem mass-spectrometric method for the enantio-selective quantification of omeprazole and its main metabolites in human serum. The method features solid-phase separation, normal phase chiral HPLC separation, and atmospheric pressure photoionization tandem mass spectrometry. The internal standards serve stable isotope labeled omeprazole and 5-hydroxy omeprazole. The HPLC part consists of Agilent 1100 system comprising a binary pump, an autosampler, a thermo-stated column component, and a diode array UV-VIS detector. The enantioselective chromatographic separation took place on a ReproSil Chiral-CA 5 ym 25 cm x 2 mm column, protected by a security guard system, equipped with a 4 mm x 2-mm silica filter insert. The analytes were detected by a Thermo Scientific TSQ Discovery Max triple quadrupole mass spectrometer, equipped with an APPI ion source with a... [Pg.232]

The same groups also reported on a 64-fold ceramic block reactor and a ceramic monolithic reactor for the screening of up to 250 catalysts in parallel (Figure 3.41). The catalyst array was prepared via an incipient wetness method by combination of different amounts of Pt, Zr and V on the alumina walls of the monolith by means of an automatic liquid handler. Gas samples from each channel of the monolith were analyzed sequentially by a quadrupole mass spectrometer by moving a capillary sampling line into the channels with the help of a three-dimensional positioning system [69],... [Pg.451]

A second commonly used mass analyzer is the quadrupole. A quadrupole acts as a mass filter, allowing a certain mass-to-charge ratio of ions to be transmitted while filtering out all others. The quadrupole consists of a set of four electrodes positioned in an array. Superimposed radio frequency and direct current electric fields can be mutually tuned to allow transmission of ions of the selected mass-to-... [Pg.53]


See other pages where Quadrupole array is mentioned: [Pg.76]    [Pg.18]    [Pg.44]    [Pg.9]    [Pg.11]    [Pg.12]    [Pg.14]    [Pg.308]    [Pg.13]    [Pg.110]    [Pg.44]    [Pg.37]    [Pg.76]    [Pg.18]    [Pg.44]    [Pg.9]    [Pg.11]    [Pg.12]    [Pg.14]    [Pg.308]    [Pg.13]    [Pg.110]    [Pg.44]    [Pg.37]    [Pg.195]    [Pg.201]    [Pg.205]    [Pg.89]    [Pg.76]    [Pg.484]    [Pg.386]    [Pg.48]    [Pg.103]    [Pg.354]    [Pg.70]    [Pg.44]    [Pg.94]    [Pg.951]    [Pg.17]    [Pg.299]    [Pg.146]    [Pg.100]    [Pg.301]    [Pg.227]    [Pg.147]    [Pg.294]   
See also in sourсe #XX -- [ Pg.11 , Pg.12 ]




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