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Isoprene nitrogen dioxide reaction

The gas-phase reactivity of various terpenes has been measured. Stephens and Scott were the first to include two terpenes (pinene and a-phel-landrene) with their study of the relative reactivity of various hydrocar ns. Both monoterpenes showed the high reactivity predicted by their olefinic structure. Conversion of nitric oxide to nitrogen dioxide in e presence of isoprene is at a rate intermediate between those for ethylene and trans-2-butene, and Japar et al, reported rate constants for the a-pinene and terpinolene-ozone reactions. Grimsrud et a/. measured the rate con-... [Pg.99]

As Barr et al. (2003) pointed out, the importance of such emissions is determined mainly by their impact on the three processes taking place in the atmosphere. The first consists in that such NMHCs as isoprene form in the course of carboxylization in plants and contribute much thereby to the formation of biospheric carbon cycle. The second process is connected with NMHCs exhibiting high chemical activity with respect to such main oxidants as hydroxyl radicals (OH), ozone (03), and nitrate radicals (N03). Reactions with the participation of such components result in the formation of radicals of alkylperoxides (R02), which favor efficient transformation of nitrogen monoxide (NO) into nitrogen dioxide (N02), which favors an increase of ozone concentration in the ABL. Finally, NMHC oxidation leads to the formation of such carbonyl compounds as formaldehyde (HCHO), which stimulates the processes of 03 formation. Finally, the oxidation of monoterpenes and sesquiterpenes results in the intensive formation of fine carbon aerosol with a particle diameter of <0.4 pm... [Pg.49]

Respiratory irritant mixtures can arise from environmental chemical reactions. For example, ozone reacts rapidly with terpenes under environmental ambient conditions to produce aldehydes, ketones, and carboxylic acids. Several studies that have been carried out demonstrated that reaction of ozone with a-pinene, c/-limonene, and isoprene produce low level concentrations (at or below NOEL levels) of oxidation products and that along with residual ozone and terpenes act as respiratory irritants. 1012 Table 17.3 lists the species typically contained in these mixtures along with their K values. As can be seen, the mixtures contain lipophiles (residual terpenes) and hydrophiles (the reaction products). Similar results have also been reported for environmental reaction of terpenes with ozone and nitrogen dioxide. 9 ... [Pg.264]

Further calculations were performed on 2,3-diaza-1,3-butadiene with different heterodienophiles such as ethene, formaldehyde and formaldimine showing the same exo oxygen or nitrogen lone pair preference [49] as well as on the nitro-soethene/ethene system [50]. Recently, ab initio studies have also been performed for the Lewis acid catalysed hetero Diels-Alder reaction of isoprene and sulfur dioxide by Sordo [51]. [Pg.11]


See other pages where Isoprene nitrogen dioxide reaction is mentioned: [Pg.475]    [Pg.200]   
See also in sourсe #XX -- [ Pg.206 ]




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