β Scribed by Robert E. Howard; Linda Mansker; Donald L. Thompson
No coin nor oath required. For personal study only.
We have computed cross sections for complex formation in H + OH collisions as a function of initial translational energy and OH vibrational and rotational state. The translational energy curve rises from a threshold below 0.2 eV to a maximum near 0.3 eV, then declines exponentiauy. The initial OH vibrational and rotational state strongly influences complex formation in low (0.2 ev) kinetic energy coliisions. Rotation particuhwiy enhances complex formation. At bigber kinetic energies (0.5 ev) rotation and vibration inhibit complex formation.
π SIMILAR VOLUMES
The energy dependence of the integral cross section for the electronic excitation in collisions of K and Hg is investigated for er?ergies between 50 eV and 1500 eV. By the measurement of the spectra of the emitted light the 4\*Pjn and the 4\*Pla states of poQs.sium are found to be dominant. For thes