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Alkyl nitrate RONO

Some fraction of the RO. radical pool, usually 10% or less, produce alkyl nitrate, RONO., upon reaction with NO by 5.59b. This termination step removes both a radical and a molecule of NO,. About 8% of the RO. radicals formed from the OH-/i-butane reaction will lead to nitrate when reacting with NO. As noted in Section 5.8.1, this percentage increases with the size of the hydrocarbon molecule, reaching about 33% for n-octane. The organic components of RONO. can react with OH to continue the VOC photooxidation cycle, although the possibility of re-releasing NO, as a result of these reactions is uncertain at present. [Pg.294]

Alkyl nitrates. A convenient preparation of RONO2 free of RONO uses KNO3 and boron trifluoride hydrate as nitrating agent in CH2CI2. [Pg.300]

One of the possible causes of the development of an oxidative course in the nitration lies in the thermal decomposition of nitrocompounds and alkyl nitrites [4]. RONO decomposes between 300 °C and 500 °C. For instance, ethylnitrite produces a free... [Pg.126]


See other pages where Alkyl nitrate RONO is mentioned: [Pg.404]    [Pg.546]    [Pg.250]    [Pg.240]    [Pg.205]    [Pg.1288]    [Pg.83]   
See also in sourсe #XX -- [ Pg.2 , Pg.111 , Pg.200 , Pg.295 , Pg.296 ]




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