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Spectra carbon dioxide

A particular vibration will give an absorption peak in the IR spectrum only if the dipole moment of the molecule changes dunng the vibration Which vibration of carbon dioxide the sym metric stretch or the antisymmetric stretch is infrared active 2... [Pg.586]

When levuhnic acid (CH3CCH2CH2CO2H) was hydrogenated at high pressure over a nickel catalyst at 220°C a single product C5Hg02 was isolated in 94% yield This compound lacks hydroxyl absorption in its IR spectrum and does not immediately liberate carbon dioxide on being shaken with sodium bicarbonate What is a reasonable structure for the compound" ... [Pg.828]

Fig 2 Mass spectrum of carbon dioxide. Relative peak intensities are plotted against mje. [Pg.38]

Figure 1. FT-IRRAS double modulation spectrum of six monolayers of Cadmium Arachidate on silver. The inset shows the background water vapor and carbon dioxide present in the measurement. IBM Instruments IR/90 series. Figure 1. FT-IRRAS double modulation spectrum of six monolayers of Cadmium Arachidate on silver. The inset shows the background water vapor and carbon dioxide present in the measurement. IBM Instruments IR/90 series.
Figure 7.9 Continuous-flow H NMR spectrum (400 MHz) of diallylphthalate in supercritical carbon dioxide (flow-rate 2mLmin 1, pressure approximately 136 bar, and temperature 321 K). After Richter et al. [153]. Reprinted with permission from B.E. Richter et al., Analytical Chemistry, 68, 1033-1039. Copyright (1996), American Chemical Society... Figure 7.9 Continuous-flow H NMR spectrum (400 MHz) of diallylphthalate in supercritical carbon dioxide (flow-rate 2mLmin 1, pressure approximately 136 bar, and temperature 321 K). After Richter et al. [153]. Reprinted with permission from B.E. Richter et al., Analytical Chemistry, 68, 1033-1039. Copyright (1996), American Chemical Society...
DPA) in dimethylphthalate at about 70°, yields a relatively strong blue Umax =435 nm) chemiluminescence the quantum yield is about 7% that of luminol 64>. The emission spectrum matches that of DPA fluorescence so that the available excitation energy is more than 70 kcal/mole. Energy transfer was observed on other fluorescers, e.g. rubrene and fluorescein. The mechansim of the phthaloyl peroxide/fluorescer chemiluminescence reaction very probably involves radicals. Luminol also chemiluminesces when heated with phthaloyl peroxide but only in the presence of base, which suggests another mechanism. The products of phthaloyl peroxide thermolysis are carbon dioxide, benzoic acid, phthalic anhydride, o-phenyl benzoic acid and some other compounds 65>66>. It is not yet known which of them is the key intermediate which transfers its excitation energy to the fluorescer. [Pg.81]

The presence of one carbon atom in a molecule of carbon dioxide results in registration of the molecular ion peak of m/z 44 and of the A + 1 isotopic peak of m/z 45. The intensity of the latter is 1.1 % of that of M+. It appears due to the presence of 13C02 molecules. An increase in the number of carbon atoms in a molecule leads to an increase of the intensity of the M + 1 ion peak to 1.1 n% of M+, where n is the number of carbon atoms in the molecule. To calculate the number of carbon atoms in a molecule using a mass spectrum one should divide the intensity of the M + 1 peak as a percentage of M by 1.1. The result defines the maximum possible number of carbon atoms. One should remember that calculations may be more complicated if an [M — H]+ ion peak is present. [Pg.162]

Figure 1. Auger electron spectrum of the surface of a Ru electrode before and after deactivation by reduction of carbon dioxide at higher temperatures ( 90 °C in 0.2 M Na2SC>4 at pH 4 and -0.545 V vs SCE). Figure 1. Auger electron spectrum of the surface of a Ru electrode before and after deactivation by reduction of carbon dioxide at higher temperatures ( 90 °C in 0.2 M Na2SC>4 at pH 4 and -0.545 V vs SCE).

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