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Spectral charts

Spektralanalyse, /. spectrum analysis, spektralanalytisch, a. spectroscopic, spectro-metric. — adv. by spectrum analysis. Spektral-apparat, to. spectroscopic apparatus, -beobachtung, /. spectroscopic observation, -bereich, -bezirk, to. spectral region, -farbe, /. spectral color, spectrum color, -gegend, /. spectral region, -lampe, /. spectrum lamp, -hnie, /. spectrum line, spectral line, -probe, /. spectrum test, -rohr, n.. -rohre, /. spectrum tube, spectral tube, -tafel, /. spectrum chart, spectral chart. [Pg.417]

When master plates taken with the spectrograph being used are not available it is possible to identify spectral lines by comparison with spectral charts. If charts are used, it is often necessary to make proper allowance for differences in dispersion and for differences in changes in dispersion with wavelength if the charts have been prepared using a prism spectrograph. [Pg.155]

First of all, when confronted by a set of spectral charts or data derived from them, try to determine the molecular formula. Sometimes it will be given, sometimes you can work it out. Other times, it may be obvious or at least likely from the chemical reactions involved. Sometimes you may have only a molecular weight, from the molecular ion of a MS for example. Either way, having a formula or molecular weight lets you determine the degrees of unsaturation (p. 131) and see what s left once you have determined part of the structure. [Pg.742]

The language has only five different instructions and its s)mtax is somewhat similar to Lisp commands are lists whose first element is the instruction. Som-A instructions are VAL, INS, EXE, STP and FIM and all should appear in a spectral chart (see Som-A s user manual for more details) ... [Pg.202]

At the end from the third group of paths in Table 3.76 it follows that la can only be followed by the remaining lie set of endpoints since all other were previously accommodated in the chart. Worth noted that this chart ordering was identically with that considered in previous study of Tetrahymena pyriformis in relation with the same set of chemical compounds, see Section 3.3.1 and Putz Lacrama (2007). However, will all these considerations the spectral chart of Figure 3.47 can be drawn. [Pg.538]

The spectral resolution of the most monochromatic laser yet devised, expressed as frequency of the laser emission divided by the laser linewidth, is approximately 5 x 10. The laser in question is a special-purpose He-Ne laser with a nominal wavelength of 632.8 nm (15,308 cm l or 4.74 x 10 Hz in frequency units) and a linewidth of 7 to 10 Hz. It is difficult to grasp the physical significance of this degree of resolution. One illustration is that, if the spectrum of this laser were displayed on chart paper such that the zero of electromagnetic energy were located at the sun and 15,308 cm l were located at the orbit of Earth, the width of the peak representing the output of the laser would be 3 millimeters. [Pg.463]

Table 9.8 Simplified infrared spectral correlation charts... [Pg.386]

On the other hand, noticeable cooperative preferential screw sense induction was reported in rodlike polysilane copolymers bearing (.S )-2-mcthylbutyl and 2-methylpropyl groups (10) and (R)-2-melhylbutyl and 2-methylpropyl groups (11) in isooctane (Chart 4.3). Since the UV-CD spectral features of the polysilane copolymers are almost identical with those of 4-6 and the Xmax varies sensitively with changes in the molar fraction of chiral substituents and temperature,28 the copolymer systems are suitable for testing the sergeants-and-soldiers phenomenon by their CD-UV spectra. [Pg.225]

Patents of Dow Chemicals first described 9,9-diaryl-substituted PF homopolymers 204 and 205 by Yamamoto polymerization of the corresponding 2,7-dibromo monomers [272], although the methods for monomer preparation were not described. For unsubstituted fluorenone, a convenient method for its conversion into 9,9-(4-hydroxyphenyl)-[307-309] and 9,9-(4-alkoxyphenyl)fluorenes [310] was reported previously, which included condensation of fluorenone with phenol or its ethers in acidic conditions (dry HC1 [308,309] or H2SO4 [307,311]) in the presence of (3-mcrcaptopropionic or mercaptoacetic acids. Both polymers 204 and 205 showed similar Mn 21,000 with PDI of 1.48 and 1.75, respectively, and spectral data typical for PF (205 Aabs = 389 (r 50,000 //(mol cm) APL = 417, 439, and 473 mn (THF)) (Chart 2.48). [Pg.129]

Attempt to identify the unknown labeled with a letter by matching the spectrum with a spectrum from the IR spectral library. First, take a preliminary look at the spectrum to check for obvious signs of the various functional groups (refer to Table 8.1 or a correlation chart). This will help reduce the number of possibilities. Report your decision regarding its identity to your instructor and justify your decision. [Pg.235]

The nitrosonium cation bears a formal relationship to the well-studied halogens (i.e. X2 = I2, Br2, and Cl2), with both classes of structurally simple diatomic electron acceptors forming an extensive series of intermolecular electron donor-acceptor (EDA) complexes that show well-defined charge-transfer absorption bands in the UV-visible spectral region. Mulliken (1952a,b 1964 Mulliken and Person, 1969) originally identified the three possible nonbonded structures of the halogen complexes as in Chart 7, and the subsequent X-ray studies established the axial form II to be extant in the crystals of the benzene complexes with Cl2 and Br2 (Hassel and Stromme, 1958, 1959). In these 1 1 molecular complexes, the closest approach of the... [Pg.225]

Funt et al. (1991, 1992) use a finite dimensional linear model to recover ambient illumination and the surface reflectance by examining mutual reflection between surfaces. Ho et al. (1992) show how a color signal spectrum can be separated into reflectance and illumination components. They compute the coefficients of the basis functions by finding a least squares solution, which best fits the given color signal. However, in order to do this, they require that the entire color spectrum and not only the measurements from the sensors is available. Ho et al. suggest to obtain the measured color spectrum from chromatic aberration. Novak and Shafer (1992) suggest to introduce a color chart with known spectral characteristics to estimate the spectral power distribution of an unknown illuminant. [Pg.63]


See other pages where Spectral charts is mentioned: [Pg.56]    [Pg.1]    [Pg.155]    [Pg.168]    [Pg.347]    [Pg.7]    [Pg.202]    [Pg.203]    [Pg.203]    [Pg.203]    [Pg.12]    [Pg.56]    [Pg.1]    [Pg.155]    [Pg.168]    [Pg.347]    [Pg.7]    [Pg.202]    [Pg.203]    [Pg.203]    [Pg.203]    [Pg.12]    [Pg.84]    [Pg.227]    [Pg.432]    [Pg.150]    [Pg.159]    [Pg.429]    [Pg.435]    [Pg.702]    [Pg.199]    [Pg.283]    [Pg.186]    [Pg.23]    [Pg.34]    [Pg.175]    [Pg.374]    [Pg.36]    [Pg.214]    [Pg.216]    [Pg.260]    [Pg.19]    [Pg.1]    [Pg.359]    [Pg.268]    [Pg.271]   
See also in sourсe #XX -- [ Pg.12 ]




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