RATE CONSTANTS FOR OZONE FORMATION

被引:18
作者
GROSS, A
BILLING, GD
机构
[1] Department of Chemistry, H.C. Ørsted Institute, University of Copenhagen
关键词
D O I
10.1016/0301-0104(94)89015-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The dynamics of collisions between an Ar atom and quasi-bound ozone, formed by colliding O2 with O to form O3*, has been studied using the quasiclassical trajectory method. The cross-sections and rate constants for stabilizing the highly exited quasi-bound ozone complex by the process O3* + Ar --> O3 + Ar, have been determined. As potential energy surface for the Ar-O3 system we use the ground state potential energy surface for ozone obtained by Sheppard and Walker (SW) coupled with an atom-atom potential for the intermolecular V(Ar)-O3 interaction. Due to the lack of a specifically calculated Ar-O3 potential, we used the Ar-O interaction from Ar-glyoxal.
引用
收藏
页码:329 / 335
页数:7
相关论文
共 7 条
[1]   MECHANICS OF ATOMIC RECOMBINATION REACTIONS [J].
BUNKER, DL .
JOURNAL OF CHEMICAL PHYSICS, 1960, 32 (04) :1001-1005
[2]   RATE CONSTANTS FOR OZONE FORMATION AND FOR ISOTOPIC EXCHANGE-REACTIONS [J].
GROSS, A ;
BILLING, GD .
CHEMICAL PHYSICS, 1993, 173 (03) :393-406
[3]   TEMPERATURE AND PRESSURE-DEPENDENCE OF OZONE FORMATION RATES IN THE RANGE 1-1000-BAR AND 90-370-K [J].
HIPPLER, H ;
RAHN, R ;
TROE, J .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (09) :6560-6569
[4]   VIBRATIONAL-RELAXATION OF GLYOXAL IN COLLISIONS WITH HE AND AR [J].
KROES, GJ ;
RETTSCHNICK, RPH .
CHEMICAL PHYSICS, 1991, 156 (02) :293-307
[5]   WIGNER METHOD STUDIES OF OZONE PHOTO-DISSOCIATION [J].
SHEPPARD, MG ;
WALKER, RB .
JOURNAL OF CHEMICAL PHYSICS, 1983, 78 (12) :7191-7199
[6]   NEW ABINITIO POTENTIAL SURFACES AND 3-DIMENSIONAL QUANTUM DYNAMICS FOR TRANSITION-STATE SPECTROSCOPY IN OZONE PHOTODISSOCIATION [J].
YAMASHITA, K ;
MOROKUMA, K ;
LEQUERE, F ;
LEFORESTIER, C .
CHEMICAL PHYSICS LETTERS, 1992, 191 (06) :515-520
[7]  
YAMASHITA K, COMMUNICATION