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Dispersive monochromator

A monochromator disperses light into its component wavelengths and selects a narrow band of wavelengths to pass on to the sample or detector. The monochromator in Figure 20-2 consists of entrance and exit slits, mirrors, and a grating to disperse the light. Prisms were used instead of gratings in older instruments. [Pg.429]

The dispersive element is contained within a monochromator. Figure 2.3a shows the optical path of an infrared spectrometer which uses a grating monochromator. Dispersion occurs when energy falling on the... [Pg.22]

The electrons emitted by the photocathode are subsequently accelerated to 50 kV and focused on to a toroid-shaped anode. The anode is made of oxygen-free, high conductivity copper and is maintained at a high positive potential. The electron pulses interact with the copper anode forcing the emission of Cu-Ka x-ray photon pulses, which exit the vacuum chamber through a thin beryllium-foil window. A bend germanium crystal monochromator disperses and focuses the x-rays onto the sample. The duration of the x-ray pulses is measured by a Kentech x-ray streak camera fitted with a low density Csl photocathode. The pulse width of the x-rays at 50 kV anode-cathode potential difference is about 50 ps. This value is an upper limit for the width of the x-ray pulses because the transit time-spread of the streak camera has to be taken into consideration. A gold photocathode (100 A Au on 1000 A peiylene) is used to record the 266-nm excitation laser pulses. The intensity of the x-rays is 6.2 x 10 photons an r (per pulse), and is measured by means of a silicon diode array x-ray detector which has a known quantum efficiency of 0.79 for 8 kV photons. [Pg.71]

One further point to note is that a grating monochromator disperses light in a series of orders. Thus a monochromator setting at 500 mn will also pass light whose wavelength is 250 nm since the second order of dispersion of li t at X will occur at 2Xj. Placing an appropriate cut-off filter after a monochromator, i.e. a P3nrex filter in this example, can efficiently remove this second-order dispersion. [Pg.43]

The dispersion of a grating refers to how broadly the monochromator disperses (or spreads) the light spectrum at the sample specimen position. Dispersion is generally expressed in units of nm per millimeter. Dispersion depends on the groove density (number of grooves per millimeter) of the grating. [Pg.13]

The basic optical configuration for UV-VIS-NIR instrumentation is shown in (Figs. 1-5). Double-monochromator (dispersive Fig. 1) instruments... [Pg.30]

Single monochromators (dispersive Fig. 2) are lower cost than doublemonochromator systems and are generally used as work horses within the laboratory. These systems typically meet the basic requirements for routine quantitative and qualitative work for relatively nondemanding applications. The dynamic range of these systems is stray light limited. [Pg.31]

Resolution is defined as the product of monochromator dispersion J, in cm V(n iw of slit width), and mechanical slit opening S, in mm, corrected for diffraction effects D from the slit jaws. It is also defined as the spacing in cm between two bands which the instrument is just capable of recognizing as two bands. [Pg.73]

The first requirement is a source of infrared radiation that emits all frequencies of the spectral range being studied. This polychromatic beam is analyzed by a monochromator, formerly a system of prisms, today diffraction gratings. The movement of the monochromator causes the spectrum from the source to scan across an exit slit onto the detector. This kind of spectrometer in which the range of wavelengths is swept as a function of time and monochromator movement is called the dispersive type. [Pg.57]

Typical grating monochromator with inset showing the dispersion of the radiation by the diffraction grating. [Pg.378]

Figure 8.28 shows how the X-rays fall on the solid or liquid sample which then emits X-ray fluorescence in the region 0.2-20 A. The fluorescence is dispersed by a flat crystal, often of lithium fluoride, which acts as a diffraction grating (rather like the quartz crystal in the X-ray monochromator in Figure 8.3). The fluorescence may be detected by a scintillation counter, a semiconductor detector or a gas flow proportional detector in which the X-rays ionize a gas such as argon and the resulting ions are counted. Figure 8.28 shows how the X-rays fall on the solid or liquid sample which then emits X-ray fluorescence in the region 0.2-20 A. The fluorescence is dispersed by a flat crystal, often of lithium fluoride, which acts as a diffraction grating (rather like the quartz crystal in the X-ray monochromator in Figure 8.3). The fluorescence may be detected by a scintillation counter, a semiconductor detector or a gas flow proportional detector in which the X-rays ionize a gas such as argon and the resulting ions are counted.
Additions to the PLM include monochromatic filters or a monochromator to obtain dispersion data (eg, the variation in refractive index with wavelength). By the middle of the twentieth century, ultraviolet and infrared radiation were used to increase the identification parameters. In 1995 the FTIR microscope gives a view of the sample and an infrared absorption pattern on selected 100-p.m areas (about 2—5-ng samples) (37). [Pg.334]

Quartz also has modest but important uses in optical appHcations, primarily as prisms. Its dispersion makes it useful in monochromators for spectrophotometers in the region of 0.16—3.5 m. Specially prepared optical-quality synthetic quartz is requited because ordinary synthetic quartz is usually not of good enough quality for such uses, mainly owing to scattering and absorption at 2.6 p.m associated with hydroxide in the lattice. [Pg.521]

A dispersive element for spectral analysis of PL. This may be as simple as a filter, but it is usually a scanning grating monochromator. For excitation spectroscopy or in the presence of much scattered light, a double or triple monochromator (as used in Raman scattering) may be required. [Pg.383]

The PIA-investigations were carried out under dynamic vacuum (p< 10 5 mbar) and at 77 K with films cast from toluene solution onto KBr substrates. For the dispersive method [29, 30] the globar, the KBr-prism premonochromator, and the grating monochromator of a Perkin Elmer 125 lR-spcctrometer were used in the spectral range of 0.25 to 1.24 eV. The pump beam was chopped mechanically... [Pg.152]

A modern laser Raman spectrometer consists of four fundamental components a laser source, an optical system for focusing the laser beam on to the sample and for directing the Raman scattered light to the monochromator entrance slit, a double or triple monochromator to disperse the scattered light, and a photoelectric detection system to measure the intensity of the light passing through the monochromator exit slit (Fig. 7). [Pg.306]

In the early work of Bewick and Robinson (1975), a simple monochromator system was used. This is called a dispersive spectrometer. In the experiment the electrode potential was modulated between two potentials, one where the adsorbed species was present and the other where it was absent. Because of the thin electrolyte layer, the modulation frequency is limited to a few hertz. This technique is referred to as electrochemically modulated infrared reflectance spectroscopy (EMIRS). The main problem with this technique is that data acquisition time is long. So it is possible for changes to occur on the electrode surface. [Pg.504]

In Raman measurements [57], the 514-nm line of an Ar+ laser, the 325-nm line of a He-Cd laser, and the 244-nm line of an intracavity frequency-doubled Ar+ laser were employed. The incident laser beam was directed onto the sample surface under the back-scattering geometry, and the samples were kept at room temperature. In the 514-nm excitation, the scattered light was collected and dispersed in a SPEX 1403 double monochromator and detected with a photomultiplier. The laser output power was 300 mW. In the 325- and 244-nm excitations, the scattered light was collected with fused silica optics and was analyzed with a UV-enhanced CCD camera, using a Renishaw micro-Raman system 1000 spectrometer modified for use at 325 and 244 nm, respectively. A laser output of 10 mW was used, which resulted in an incident power at the sample of approximately 1.5 mW. The spectral resolution was approximately 2 cm k That no photoalteration of the samples occurred during the UV laser irradiation was ensured by confirming that the visible Raman spectra were unaltered after the UV Raman measurements. [Pg.5]

Hadamard transform [17], For example the IR spectrum (512 data points) shown in Fig. 40.31a is reconstructed by the first 2, 4, 8,. .. 256 Hadamard coefficients (Fig. 40.38). In analogy to spectrometers which directly measure in the Fourier domain, there are also spectrometers which directly measure in the Hadamard domain. Fourier and Hadamard spectrometers are called non-dispersive. The advantage of these spectrometers is that all radiation reaches the detector whereas in dispersive instruments (using a monochromator) radiation of a certain wavelength (and thus with a lower intensity) sequentially reaches the detector. [Pg.564]


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