12 May 2017 Laser induced fluorescence spectrum analysis of OH from photo-dissociation of water in gas phase
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Proceedings Volume 10173, Fourth International Symposium on Laser Interaction with Matter; 1017311 (2017) https://doi.org/10.1117/12.2268150
Event: 4th International Symposium on Laser Interaction with Matter, 2016, Chengdu, China
Abstract
The OH can be generated from photo-dissociation of water in the gas phase, and the generated OH has served in tagging velocimetry using the time-flight method. The hydroxyl tagging mechanism has the advantages of non-seeding, kindly flow following character, but its application in the reaction region is limited for the fluorescence interference from nascent OH. In this paper, we explored the laser induced fluorescence spectrum of OH both from burning and photodissociation. A photo-dissociation laser induced fluorescence (PD-LIF) system with optical multichannel analysis instrument (OMA) for spectrum analysis was developed. Based on multichannel mechanism, the LIF spectrum of OH from photo-dissociation and burning were acquired simultaneously. The temporal spectrum profiles of dissociation OH both in flame and air were taken by varying the pump–probe delay. The normalized emission spectrum in flame showed a process of rotational relaxation while in air the spectrum was almost not changed. The fluorescence intensity was precisely proportional to the base states population, so we can get certain states that the OH from dissociation was predominant from the fluorescence intensity ratio of OH. This result can be further utilized for hydroxyl tagging velocimetry technology (HTV) which was less affected by burning OH.
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Guohua Li, Guohua Li, Jingfeng Ye, Jingfeng Ye, Zhengrong Zhang, Zhengrong Zhang, Sheng Wang, Sheng Wang, Zhiyun Hu, Zhiyun Hu, Xinyan Zhao, Xinyan Zhao, } "Laser induced fluorescence spectrum analysis of OH from photo-dissociation of water in gas phase", Proc. SPIE 10173, Fourth International Symposium on Laser Interaction with Matter, 1017311 (12 May 2017); doi: 10.1117/12.2268150; https://doi.org/10.1117/12.2268150
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