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Spectrum stabilization

Over a period of time, it is possible that a spectrum will drift so causing the peaks to broaden and, in extreme cases. [Pg.94]

My own experience has been that, in a temperature-controlled laboratory for routine measurements, spectrum stabilization is not necessary. Unexpected spectrum shifts are occasionally experienced but these have usually been attributable to malfunction of the temperature control. However, in environments less comfortable than a clean temperature-controlled counting room and at high count rates the ability to stabilize the spectrometer may be welcome. [Pg.95]

Analogue stabilization is only suitable for low-resolution spectrometry. Scintillation detectors are particularly prone to drift because of the temperature sensitivity of the electronics and to instabUity of tbe high voltage. This form of [Pg.95]

In order for the analogue stabilizer to operate successfully it is, of course, necessary for there to be a prominent high-energy peak in the spectrum. If there were no such peak, one would have to be introduced by an external source not a particularly good solution because of the Compton contribution to the rest of the spectrum. Because it takes place external to the MCA, analogue stabilization does not take into account MCA drift. It is difficult to set up and operate and, even on low-resolution systems, thejob could be better done by using digital stabilization. [Pg.95]

For Nal(Tl) scintillation systems, it is possible to buy a detector that contains a small amount of Am. This is said to be seeded . The 59.54keV gamma-ray from the Am provides a well-defined peak at low energy for the spectrum stabilizer to work on, and the alpha particles provide a peak above 3 MeV as a high-energy marker. [Pg.95]


The polymeric phenolic phosphites are excellent heat and processing stabilizers and can contribute significantly to photostability. These broad-spectrum stabilizers offer possibilities for simplifying polypropylene stabilizer systems. They may allow one to use lesser amounts of other additives, and they open up a new area for potential cost savings in formulating polypropylene resins. [Pg.238]

The penicillins [pen i SILL in] are the most widely effective antibiotics and are among the least toxic drugs known the major adverse reaction to penicillins is hypersensitivity. The members of this family differ from one another in the R substituent attached to the 6-aminopenicillanic acid residue. The nature of this side chain affects their antimicrobial spectrum, stability to stomach acid, and susceptibility to bacterial degradative enzymes (P-lactamases). Figure 30.1 shows the main structural features of the penicillins. Figure 30.2 shows the classification of agents affecting cell wall synthesis. [Pg.308]

A spectrum stabilizer will be useful if the system is subject to poorly controlled environmental conditions, especially temperature change, or is used at high count rates. For germanium detector systems, the digital stabilizer is recommended. [Pg.99]

Cyclopentadienyl radicals have been known as long-lived species since Ziegler and Schnell reported the pentaphenyl derivative in 1925, and many differently substituted derivatives have been prepared. The ESR spectra of the parent cyclopentadienyl radical 6 as well as a variety of monosubstituted derivatives RC5H4 (R = D, Me, Et, i-Pr, and t-Bu) f were measured in solution. The spectrum of 6 favors a planar Ti-radical with average Dsh symmetry. This radical is expected to exist as an equilibrium mixture of five pairs of C v structures due to Jahn— Teller distortion, with a very low barrier for rearrangement. Above 70 K, all five hydrogen atoms are equivalent in the ESR spectrum, although in matrixes below this temperature the spectrum is more complex, which is ascribed to observation of the Jahn—Teller-distorted C2 spectrum stabilized by the matrix. ... [Pg.12]

Available stability constants for the formation of various chloro complexes in anhydrous methanol are reported in table 3. Kozachenko and Batyaev (1971a) investigated the inner- and outer-sphere chloride complex formation in absolute and aqueous methanol for all the lanthanides which have absorption bands in the UV and visible parts of the spectrum. Stability constant data for absolute methanol reveal a slight increase in the degree of complex formation in the series Pr—Nd-Sm, followed by a decrease for the heavier lanthanide ions. Ho and Er. The stability constants are approximately three times larger than in 50% methanol and 8-9 times larger than in water. The estimated jSi s ( 0.1) amount to 0.71 (Nd), 0.82 (Nd), 1.24 (Sm), 0.50 (Ho), and 0.47 (Er). [Pg.327]

Figure 7.3 Efficiency of the active spectrum stabilization (a) displacements parallel to the echelle dispersion (b) displacements perpendicular to the echelle dispersion (black spectrograph temperature blue position of the Ne reference line at 614.306 nm red position of the Zn sample line at 213.856 nm)... Figure 7.3 Efficiency of the active spectrum stabilization (a) displacements parallel to the echelle dispersion (b) displacements perpendicular to the echelle dispersion (black spectrograph temperature blue position of the Ne reference line at 614.306 nm red position of the Zn sample line at 213.856 nm)...
Formaldehyde Low costs Broad antimicrobial spectrum Stability Easy application Resistance in some organisms Tbxicity Suspected of promoting cancer Reacts with protein-fixing biofilms on surfaces Legal restrictions... [Pg.212]

The hindered piperidines exhibit a complex behaviour when present in combination with other antioxidants and stabilizers. As discussed earlier (see Section 19.4.2.1), these have to be oxidized first to the corresponding nitroxyl radicals before becoming effective. Consequently, both CB-D and PD-C antioxidants which remove alkylperoxyl radicals and hydroperoxides respectively, antagonize the UV stabilizing action of this class of compounds. However, since the hindered piperidines themselves are neither melt nor heat stabilizers for polymers, they have to be used with conventional antioxidants and stabilizers. By contrast, the derived nitroxyl radicals are much more effective broad spectrum stabilizers, since not only are they more effective UV stabilizers but they are also highly efficient melt stabilizers and have some thermal antioxidant activity. Hindered piperidines have been reported to synergize with UV absorbers, e.g. the benzotriazole UV stabilizers, in different polymers such as polypropylene, polystyrene and ABS. ... [Pg.1337]


See other pages where Spectrum stabilization is mentioned: [Pg.265]    [Pg.336]    [Pg.2859]    [Pg.20]    [Pg.198]    [Pg.137]    [Pg.94]    [Pg.95]    [Pg.95]    [Pg.53]    [Pg.87]    [Pg.72]    [Pg.1317]    [Pg.445]    [Pg.538]    [Pg.538]   


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