Reactions of protonated water clusters with chlorine nitrate revisited
被引:9
作者:
Gilligan, JJ
论文数: 0引用数: 0
h-index: 0
机构:
Penn State Univ, Dept Chem, University Pk, PA 16802 USAPenn State Univ, Dept Chem, University Pk, PA 16802 USA
Gilligan, JJ
[1
]
Moody, DJ
论文数: 0引用数: 0
h-index: 0
机构:Penn State Univ, Dept Chem, University Pk, PA 16802 USA
Moody, DJ
Castleman, AW
论文数: 0引用数: 0
h-index: 0
机构:Penn State Univ, Dept Chem, University Pk, PA 16802 USA
Castleman, AW
机构:
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Phys, University Pk, PA 16802 USA
来源:
ZEITSCHRIFT FUR PHYSIKALISCHE CHEMIE-INTERNATIONAL JOURNAL OF RESEARCH IN PHYSICAL CHEMISTRY & CHEMICAL PHYSICS
|
2000年
/
214卷
/
10期
关键词:
water clusters;
chlorine nitrate;
atmospheric chemistry;
ion-molecule reactions;
D O I:
10.1524/zpch.2000.214.10.1383
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:
Potential reaction mechanisms of D+(D2O)(n) (n = 4-30) with chlorine nitrate (ClONO2) have been investigated using a fast flow reactor operated under thermal conditions. Chemical reactions are not observed to occur between D+(D2O)(n) and chlorine nitrate. Instead, through studies employing the heavy isotope of hydrogen, we found that the nitric acid observed in the product ion spectrum arises from a nitric acid impurity that is usually present to some degree in the methods employed to synthesize ClONO2 reactant gas. The results from this study serve to explain other conflicting reaction mechanisms reported in the literature, and which have been discussed in the context of atmospheric chemistry.