Diode array spectrometer

M. F. Pimentel, B. De Narros Neto, M. C. Ugulino de Araujo and C. Pasquini, Simultaneous multielemental determination using a low-resolution inductively coupled plasma spectrometer/diode array detection system, Spectrochim. Acta, Part B, 52(14), 1997, 2151-2161. 

In one instrument, ions produced from an atmospheric-pressure ion source can be measured. If these are molecular ions, their relative molecular mass is obtained and often their elemental compositions. Fragment ions can be produced by suitable operation of an APCI inlet to obtain a full mass spectrum for each eluting substrate. The system can be used with the effluent from an LC column or with a solution from a static solution supply. When used with an LC column, any detectors generally used with the LC instrument itself can still be included, as with a UV/visible diode array detector sited in front of the mass spectrometer inlet. 

Figura 3 Grating spectrometers commonly used for ICP-OES (a) monochromator, in which wavelength is scanned by rotating the grating while using a singie photomultiplier tube (PMT) detector (b) polychromator, in which each photomultiplier observes emission from a different wavelength (40 or more exit slits and PMTs can be arranged along the focal plane) and (c) spectrally segmented diode-array spectrometer.

G. M. Levy, A. Quaglia, R, E. Lazure, and S. W. McGeorge. Spect. Acta. 42B, 341, 1987. Describes the diode array-based spectrally segmented spectrometer for simultaneous multielement analysis. 

The intensity of absorbed radiation. Sunlight or room lights may alter the rate of a reaction. Usually this effect is to be avoided unless the object is to study photochemical effects. The light level in an optical spectrometer that uses monochromatic light is not likely to cause problems, but if white light strikes the sample, as in a diode-array spectrophotometer, this is a possibility. 

A more definitive identification may be obtained by combining retention characteristics with more specific information from an appropriate detector. Arguably, the most information-rich HPLC detectors for the general identification problem are the diode-array UV detector, which allows a complete UV spectrum of an analyte to be obtained as it elutes from a column, and the mass spectrometer. The UV spectrum often allows the class of componnd to be determined but the... 

A modern spectrophotometer (UV/VIS, NIR, mid-IR) consists of a number of essential components source optical bench (mirror, filter, grating, Fourier transform, diode array, IRED, AOTF) sample holder detector (PDA, CCD) amplifier computer control. Important experimental parameters are the optical resolution (the minimum difference in wavelength that can be separated by the spectrometer) and the width of the light beam entering the spectrometer (the fixed entrance slit or fibre core). Modern echelle spectral analysers record simultaneously from UV to NIR. 

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. 

The scope of UV analysis of dissolved polymer/additive matrices is thus quite restricted and mainly limited to special cases in which the additive package is known, e.g. the determination of Irganox 1098 in GFR-PA4.6 after dissolution in H2SO4/HNO3. Fibre-optic dissolution analysis by means of a UV diode array spectrometer is well known. In comparison to IR spectroscopy, UV spectrophotometry is better equipped to provide quantitative data. 

The quaternization kinetics were followed by 3H NMR spectroscopy using a JE0L FX-90Q NMR spectrometer. Solvolysis of p nitro-phenylacetate was followed by UV spectroscopy using a Hewlett Packard 8450 A diode array spectrophotometer. 

The most commonly used method for the identification of carotenoids is high-pressure liquid chromatography (HPFC) combined with the UV-Vis absorption detection. The introduction of diode array detection enabled parallel collection of pigment spectra, which greatly aids the quantification and localization of unknown compounds. Coupling HPFC with the mass-spectrometer significantly... 

Topics which will be presented in this chapter include the hardware, software, automation, valve and column configurations, and integration used in comprehensive 2DLC. Aspects of the 2DLC experiment in conjunction with multichannel detectors such as UV diode array optical detectors and mass spectrometers are discussed along with the handling of the data, which is expected to expand in scope in the future as chemometric methods are more widely used for data analysis. 

In order to observe a short-lived species it may be necessary to employ a rapid-scanning spectrometer, such as a diode-array instrument (Sms for a 240nm-800nm spectrum). In addition, the absorbances of electrogenerated species can be very small and signal-averaging or phase-sensitive detection may be necessary to achieve the required signal-to-noise ratio (cf. EMIRS and FTIR). 

---