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Absorption spectrometer, operation

Potassium at trace concentrations in aqueous samples can be measured by a flame photometer at a wavelength of 766.5 nm. Either a flame photometer or an atomic absorption spectrometer operating in flame emission mode can be used for such analysis. [Pg.736]

Zeeman/3030 Atomic Absorption Spectrometer, Operator s Manual, Perkin Elmer,... [Pg.41]

The following NMR absorptions were obtained on a spectrometer operating at 200 MHz and are given in hertz downfield from the TMS standard. Convert the absorptions to 5 units. [Pg.471]

When measured on a spectrometer operating at 200 MHz, chloroform (CHCI3) shows a single sharp absorption at 7.3 8. [Pg.472]

Chemical shift (Section 13.3) The position on the NMR chart where a nucleus absorbs. By convention, the chemical shift of tetramethylsilane (TMS) is set at zero, and all other absorptions usually occur downfield (to the left on the chart). Chemical shifts are expressed in delta units. 5, w here 1 5 equals 1 ppm of the spectrometer operating frequency. [Pg.1237]

At present, however, the usual flame emission method is obtained by simply operating a flame atomic absorption spectrometer in the emission mode (see Fig. 21.3). [Pg.797]

Figure 5.17. Dual-column ion exchange preconcentration valve. Sa, Sb samples A and B Ca, Cb ion exchange columns A and B Ea, Eb eluant (2 M nitric acid) for columns A and B Wa, Wb waste lines for samples and eluants A and B W waste lines AAS atomic absorption spectrometer. The dimensions of the base plate of the valve are 70 x 45 x 10 mm. See text for details of operation. Source [661]... Figure 5.17. Dual-column ion exchange preconcentration valve. Sa, Sb samples A and B Ca, Cb ion exchange columns A and B Ea, Eb eluant (2 M nitric acid) for columns A and B Wa, Wb waste lines for samples and eluants A and B W waste lines AAS atomic absorption spectrometer. The dimensions of the base plate of the valve are 70 x 45 x 10 mm. See text for details of operation. Source [661]...
The design of a conventional atomic absorption spectrometer is relatively simple (Fig. 3.1), consisting of a lamp, a beam chopper, a burner, a grating monochromator, and a photomultiplier detector. The design of each of these is briefly considered. The figure shows both single and double beam operation, as explained below. [Pg.50]

FIA star 5010 Modular, semi- or fully automatic operation. May be operated with process controller microprocessor. Can be set up in various combinations with 5017 sampler and superflow software which is designed to run on IBM PC/XT computer 60-180 samples h Dialysis for in-line sample preparation and in-line solvent extraction.Thermostat to speed up reactions. Spectrophotometer (400-700nm) or photometer can be connected to any flow through detector, e.g. UV/visible, inductively coupled plasma, atomic absorption spectrometer and ion-selective electrodes... [Pg.35]

B.3 Operation and Optimization of an Atomic Absorption Spectrometer and Determination of Magnesium in Synthetic Human Urine. [Pg.163]

When Walsh started to think about using AAS for analytical purposes back in 1952, one of his key conclusions was that, in order to carry out absorption measurements on luminous atomic vapors, it would be necessary to employ a modulated light source and a synchronously tuned detection system, so that any radiation emitted by the sample would produce no signal at the output of the detection system [2]. This modulation principle, using either an AC-operated radiation source or a chopper in the radiation beam, and a selective amplifier tuned to the same modulation frequency, has ever since been applied in all commercially available atomic absorption spectrometers. It has been considered one of the major advantages of... [Pg.87]

It passes through the sample absorption cell made of Pyrex with polyethylene windows and is detected with a liquid helium cooled bolometer. One of the lasers is frequency-modulated at 1 kHz and the detector output is processed with a lock-in amplifier, as shown. Far-infrared rotational spectra of CO, HC1 and HF have been recorded [67], and as an example of the excellent sensitivity achieved, we refer the reader to the spectrum of the OH radical [68] shown later in this chapter. Evenson s spectrometer operates over a wide range of the far-infrared region up to 9 THz, with excellent frequency stability. [Pg.728]

To measure the ultraviolet (or UV-visible) spectrum of a compound, the sample is dissolved in a solvent (often ethanol) that does not absorb above 200 nm. The sample solution is placed in a quartz cell, and some of the solvent is placed in a reference cell. An ultraviolet spectrometer operates by comparing the amount of light transmitted through the sample (the sample beam) with the amount of light in the reference beam. The reference beam passes through the reference cell to compensate for any absorption of light by the cell and the solvent. [Pg.698]

The general construction of an atomic absorption spectrometer, which need not be at all complicated, is shown schematically in Fig. 1. The most important components are the light source (A), which emits the characteristic narrow-line spectrum of the element of interest an absorption cell or atom reservoir in which the atoms of the sample to be analysed are formed by thermal molecular dissociation, most commonly by a flame (B) a monochromator (C) for the spectral dispersion of the light into its component wavelengths with an exit slit of variable width to permit selection and isolation of the analytical wavelength a photomultiplier detector (D) whose function it is to convert photons of light into an electrical signal which may be amplified (E) and eventually displayed to the operator on the instruments readout, (F). [Pg.15]

The introduction of a simple microprocessor into an atomic absorption spectrometer has increased flexibility and ease of operation. The following benefits have been introduced (a) Easier operation via a keyboard and push... [Pg.35]

The resonance frequency measured in NMR is normally expressed in terms of units independent of the spectrometer field strength and hence as a chemical shift (8) in parts per million with respect to a reference compound [i.e.,8 = (// ampic - f/rcfere,.ceVv,(10 ), where and are positions of the respective absorption lines (in Hz) and v is the spectrometer operating frequency]. [Pg.73]

The position on the chart at which a nucleus absorbs is called its chemical shift. The chemical shift of TMS is set as the zero point, and other absorptions normally occur downfield, to the left on the chart. NMR charts are calibrated using an arbitrary scale called the delta ((5) scale, where 1 5 equals 1 part per million (1 ppm.) of the spectrometer operating frequency. For example, if we w ere measuring the NMR spectrum of a sample using an instrument operating at... [Pg.445]

Jrlow many hertz downfield from TMS would chloroform absorb if the measurement were carried out on a spectrometer operating at 360 MHz (c) What would be the position of the chloroform absorption in 8 units when measured on a 360 MHz spectrometer ... [Pg.472]


See other pages where Absorption spectrometer, operation is mentioned: [Pg.29]    [Pg.58]    [Pg.259]    [Pg.334]    [Pg.464]    [Pg.29]    [Pg.58]    [Pg.259]    [Pg.334]    [Pg.464]    [Pg.441]    [Pg.134]    [Pg.567]    [Pg.25]    [Pg.52]    [Pg.57]    [Pg.152]    [Pg.272]    [Pg.154]    [Pg.70]    [Pg.721]    [Pg.78]    [Pg.16]    [Pg.925]    [Pg.145]    [Pg.6]    [Pg.607]    [Pg.275]    [Pg.155]    [Pg.161]    [Pg.244]   
See also in sourсe #XX -- [ Pg.503 ]




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