Variational transition state theory calculations of the reaction rates of F with H2, D2, and HD and the intermolecular and intramolecular kinetic isotope effects

Technical Report · Sat Jun 15 00:00:00 EDT 1985

OSTI ID:6130399

Steckler, R; Truhlar, D G; Garrett, B C

Variational transition state theory is used to calculate rate constants and kinetic isotope effects for the reactions F + H2 yields HF + H(with rate constant k sub 1), F + D2 yields DF + D(k sub 2), and two other isotopic analogs as functions of temperature. The calculations are performed using a recently proposed partly empirical, partly ab initio potential energy surface, called surface No. 5, and also using a new surface, called surface No. 5A, introduced here to test the effect of a higher classical saddle point on the reaction rates, kinetic isotope effects, and reaction thresholds. The various theoretical results are compared to the available experiments to test the validity of these potential energy surfaces. For those rate constants and kinetic isotope effects for which there is more than one experimental value at a given temperature the theoretical results for the reactions on the surface No. 5 agree wtih the experiment about as well as the individual experiments agree with each other.

• Research Organization: Chemical Dynamics Corp., Columbus, OH (USA)
• OSTI ID: 6130399
• Report Number(s): AD-A-160134/3/XAB
• Country of Publication: United States
• Language: English

Related Subjects

640304* -- Atomic
Molecular & Chemical Physics-- Collision Phenomena
74 ATOMIC AND MOLECULAR PHYSICS
ATOM COLLISIONS
ATOM-MOLECULE COLLISIONS
CHEMICAL REACTIONS
COLLISIONS
DEUTERIDES
DEUTERIUM
DEUTERIUM COMPOUNDS
ELEMENTS
ENERGY
FLUORINE
HALOGENS
HYDROGEN
HYDROGEN COMPOUNDS
HYDROGEN DEUTERIDE
HYDROGEN ISOTOPES
ISOTOPE EFFECTS
ISOTOPES
KINETICS
LIGHT NUCLEI
MOLECULE COLLISIONS
NONMETALS
NUCLEI
ODD-ODD NUCLEI
POTENTIAL ENERGY
REACTION KINETICS
STABLE ISOTOPES
SURFACES