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Glyoxal emission

Analysis. Ca gives a brick-red flame coloration, indicating that various optical spectroscopies will be effective in its determination. Ca is quantitatively determined by colorimetry down to 100 ppb using murexide or o-cresolphthalein, by atomic absorption spectroscopy (AAS) to 20 ppb, to 1 ppb by electrothermal absorption spectroscopy (ETAS), to 0.01 ppb by inductively-coupled plasma emission spectroscopy (ICPES), and to 10 ppb by inductively-coupled plasma mass spectroscopy (ICPMS). A spot test for Ca which extends to 3 ppm is provided by glyoxal bis(2-hydroxyanil). [Pg.139]

N20 emission at chemical plants and the methods of its abatement have been considered in several reviews [185-187]. The major emission is related to the preparation of nitric add and its use in oxidation processes, like those involved in the production of adipic acid, caprolactam, glyoxal, acrylonitrile, and so forth. Of them, the biggest emission is the offgases of adipic acid about 1 M MT N 20 per year with a concentration of 30-40%. Recovery and purification of N20 from these offgases for use in the oxidation of benzene to phenol are described by Uriarte [188], Some companies use these off-gases to obtain medical-grade nitrous oxide. [Pg.244]

Several of the early oxide studies have already been mentioned in the introduction. The copper-alumina oxidation catalyst, which finds applications for the synthesis of glyoxal from glycol and as the principal component of base-metal formulations for automobile exhaust emission control, has... [Pg.275]

Electronic Spectrum. The A X and B - X absorption spectrum of biacetyl is similar to that of glyoxal. The first absorption band occurs in the 470- to 340-nm region. The 0-0 band is placed at 21,983 cm l (111), and there is some vibrational structure at wavelengths greater than 400 nm. The second absorption band occurs in the 280- to 220-nm region and consists of continuous absorption only. The emission occurs only when the A state is excited. [Pg.66]

Polymer 56, soluble in DMF or DMSO, can be prepared by the condensation of amino-substituted [Ru(bpy)3]2+ with glyoxal [112]. This polymer showed weaker emission than the free Ru chromophore that was attributed to less efficient intersystem crossing to the 3MLCT state. Similar condensation reactions with diacid anhydrides to produce polyimides have been reported [113]. These polymers showed long-wavelength emission associated with charge-transfer states. [Pg.263]

Collision-induced intramolecular vibration-to-rotation energy transfer appears to be inefficient. The evidence for this inference comes from the study of rotational contours in the one collision-induced transition 7 0° in glyoxal. It is found that the emission from 0° has a distribution over rotational transitions that is close to the thermal distribution. But the vibration v-j in glyoxal is a torsional motion, and the axis of torsion very nearly coincides with the smallest axis of inertia of the molecule, so if collision-induced intramolecular vibra-tion-to-rotation transfer were efficient the emission from 0 should have a nonthermal distribution in the quantum number K (which describes quantization of the motion about the smallest axis of inertia). Note, however, that the collision partner used in this experiment was... [Pg.259]

Mylona, S. (1996) Sulphur dioxide emissions in Europe 1880-1991 and their effect on sulphur concentrations and depositions. Tellus 48B, 662-68 Myriokefalitakis, S., M. Vrekoussis, K. Tsigaridis, F. Wittrock, A. Richter, C. Bruhl, R. Volkamer, J. R Burrows and M. Kanakidou (2008) The influence of natural and anthropogenic secondary sources on the glyoxal global distribution. Atmospheric Chemistry and Physics 8, 4965-4981... [Pg.662]

Ozone reacts rapidly with alkenes to give a chemiluminescence emission from several excited-state species. Excited species identified as emitters in the ozone oxidation of ethene include formaldehyde at 350-520nm ( A2) and hydroxyl radicals at 700-1100 nm (X n, v<9) and 306 nm (A E ). In addition, phosphorescence is observed from glyoxal and methyl glyoxal ( Au are oxidized. [Pg.550]

Ballerini A, Despres A and Pizzi A (2005), Non-toxic, zero emission taimin—glyoxal adhesives for wood panels , Holz Roh Werkst, 63, 477-478. [Pg.37]

The studies of references 4-9 involve the measurement of intensities of various dispersed emission peaks as a function of different accessed vibronic transitions in clusters. The systems studied are tetrazine(Ar)i, glyoxal(Ar)i, (Kr) i, (Nili, p-difluorobenzene(Ar)i, pyrimidine(Ar)i, (N2)i, respectively. Other work is referenced in these papers. While we will not discuss the extensive detail in these papers, we will present a general discussion of their major findings and approach to their data. [Pg.299]


See other pages where Glyoxal emission is mentioned: [Pg.251]    [Pg.200]    [Pg.251]    [Pg.200]    [Pg.75]    [Pg.357]    [Pg.269]    [Pg.357]    [Pg.353]    [Pg.5]    [Pg.49]    [Pg.75]    [Pg.129]    [Pg.138]    [Pg.462]    [Pg.238]    [Pg.261]    [Pg.292]    [Pg.62]    [Pg.112]    [Pg.198]    [Pg.383]    [Pg.384]    [Pg.878]    [Pg.24]    [Pg.1055]    [Pg.1367]    [Pg.1390]   
See also in sourсe #XX -- [ Pg.198 ]




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