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Bromine atom velocity

These assumptions lead, by the same method of calculation as that used in the case of the thermal reaction, to the correct velocity equation. It is to be noted that since (2) is followed by either (3) or (4) the actual formation of hydrobromic acid does not use up the supply of atomic bromine, and a stationary concentration of bromine atoms is established by the balancing of the rate of their photochemical formation (1) and the rate of their thermal recombination (5). ... [Pg.86]

In the well-known mechanism for the hydrogen-bromine reaction one may for instance not be inclined to consider the bromine atoms as a catalyst. As a matter of fact their concentration can be increased at will within limits by irradiation of the mixture (16) which causes a definite increase of the velocity of the overall reaction, an effect which may very well be called catalytic. [Pg.321]

The case is different when the catalyst is formed by the system itself. In these cases one extra condition is required to determine the velocity. In the hydrogen-bromine reaction the bromine atoms are formed by the dissociation of bromine molecules and disappear by the reversed reaction. Steady course of the reaction thus requires that chemical equilibrium in regard to that reaction is reached. [Pg.321]

Fig. 7. Proton stopping cross section in atomic gaseous targets (a) Oxygen, (b) Argon, (c) Bromine as a function of projectile velocity (atomic units). (—) OLPA-TFD(l/8)W... Fig. 7. Proton stopping cross section in atomic gaseous targets (a) Oxygen, (b) Argon, (c) Bromine as a function of projectile velocity (atomic units). (—) OLPA-TFD(l/8)W...
In Tables -A, we report oscillator strengths for some fine structure transitions in neutral fluorine, chlorine, bromine and iodine, respectively. Two sets of RQDO/-values are shown, those computed with the standard dipole length operator g(r) = r, and those where core-valence correlation has been explicitly introduced, Eq. (10). As comparative data, we have included in the tables /-values taken from critical compilations [15,18], results of length and velocity /-values by Ojha and Hibbert [17], who used large configuration expansions in the atomic structure code CIVS, and absolute transition probabilities measured through a gas-driven shock tube by Bengtson et al. converted... [Pg.267]

Bunnett and Conner" determined velocities and equilibria for the interchange of chlorine, bromine, and Iodine atoms in the hulugeno-2,4-dinitrohcnzenes. [Pg.898]

Arthur Suits is a professor of chemistry at Wayne State University where he and his group study the many roles office radicals—atoms or molecules with unpaired electrons—in chemical processes. One of the techniques developed in his lab, DC Shce Velocity Map Imaging, uses a video camera to record images of ions formed by photo ionization after (for one example) a dissociation reaction occurs. For instance, Suits has used laser photodissociation (Section 7.4) to break deuterium bromide ( HBr or DBr) into deuterium and bromine radicals. The photodissociation occurs at a fixed photon energy... [Pg.319]


See other pages where Bromine atom velocity is mentioned: [Pg.50]    [Pg.322]    [Pg.13]    [Pg.178]    [Pg.313]    [Pg.201]    [Pg.161]    [Pg.7]    [Pg.267]    [Pg.179]    [Pg.334]    [Pg.906]    [Pg.179]    [Pg.284]    [Pg.311]    [Pg.210]   
See also in sourсe #XX -- [ Pg.201 ]




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Bromine atoms

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