On the vibrational excitation of shock-heated air. II. CO as a tracer and its oxidation

D Dong He (School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus) Q Qizhen Hong (State Key Laboratory of High Temperature Gas Dynamics, Institute of Mechanics, Chinese Academy of Sciences 1 , 100190 Beijing,) F Fernando Pirani (Dipartimento di Chimica, Biologia e Biotecnologie, Università di Perugia 2 , via Elce di Sotto 8, 06123 Perugia,) R Renjie Li (Songshan Lake Materials Laboratory) F Fei Li Q Quanhua Sun (State Key Laboratory of High Temperature Gas Dynamics, Institute of Mechanics, Chinese Academy of Sciences 1 , 100190 Beijing,) T Ting Si (Deep Space Exploration Laboratory, State Key Laboratory of High Temperature Gas Dynamics, Department of Modern Mechanics, University of Science and Technology of China 1 , Hefei 230026,) X Xisheng Luo (Deep Space Exploration Laboratory, State Key Laboratory of High Temperature Gas Dynamics, Department of Modern Mechanics, University of Science and Technology of China 1 , Hefei 230026,)

Abstract

This is the second part of a series of papers aiming to investigate the vibrational excitation behavior of shock-heated high-temperature air by using CO as a tracer. In this study, the absorbance features and rovibrational temperature time histories are used to study the vibrational relaxation behaviors of CO/O2/N2/Ar mixtures at 1700–3360 K by combining shock tube and laser absorption spectroscopy. State-to-state modeling using our developed vibrational state-specific rate coefficients shows close agreement with the absorbance features and temperature time histories. In contrast, the use of the Schwartz–Slawsky–Herzfeld formula under mode assumptions fails in accurately reproducing the experimental results. Sensitive vibrational–vibrational relaxation data between O2 and N2 are extracted from the present experiments. Systematic deviations from literature values are identified and discussed, with differences attributed primarily to variations in post-processing approaches. The present study concludes that a small amount of CO can effectively trace the vibrational relaxation behaviors of the air mixture. In addition, characteristic times of CO oxidation derived from laser absorption spectroscopy measurements are summarized, exhibiting a near-linear dependence on T−1/3.

Article Details

Volume / Issue Vol. 164, Issue 16
Published April 28, 2026
ISSN 0021-9606
Publisher American Institute of Physics

Journal Info

The Journal of Chemical Physics

American Institute of Physics

ISSN: 0021-9606 Physical Sciences

Authors (8)

D

Dong He

School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus

Q

Qizhen Hong

State Key Laboratory of High Temperature Gas Dynamics, Institute of Mechanics, Chinese Academy of Sciences 1 , 100190 Beijing,

F

Fernando Pirani

Dipartimento di Chimica, Biologia e Biotecnologie, Università di Perugia 2 , via Elce di Sotto 8, 06123 Perugia,

R

Renjie Li

Songshan Lake Materials Laboratory

F

Fei Li

Q

Quanhua Sun

State Key Laboratory of High Temperature Gas Dynamics, Institute of Mechanics, Chinese Academy of Sciences 1 , 100190 Beijing,

T

Ting Si

Deep Space Exploration Laboratory, State Key Laboratory of High Temperature Gas Dynamics, Department of Modern Mechanics, University of Science and Technology of China 1 , Hefei 230026,

X

Xisheng Luo

Deep Space Exploration Laboratory, State Key Laboratory of High Temperature Gas Dynamics, Department of Modern Mechanics, University of Science and Technology of China 1 , Hefei 230026,