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Mechanism of inhibition by isobutene

When a mixture of neopentane and isobutene is pyrolysed, the primary mechanism of [Pg.175]

The isobutenyl free radical CH2-C(CH3)=CH2 is stabilized by resonance and, consequently, is much less reactive than the neopentyl or the methyl radical. Two consequences result from this  [Pg.176]

The new rate laws, which take the reactions (67) to (69) into account, can be established using the global QSSA  [Pg.176]

Relationships (70) and (71) can be simplified using the so-called crossed-constants approximation, coming from the kinetic theory of gases  [Pg.176]

Tq is the rate of formation of CH, at conversion of C3Hj2 equal to zero, in the absence of C4Hg, whereas r is the rate, still at zero conversion of C3HJ25 but in the presence ofC4Hg. [Pg.177]


See other pages where Mechanism of inhibition by isobutene is mentioned: [Pg.175]   


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