{"title":"0.16 ~ 1.20 Bar压力下03/02混合物的脉冲co2 -激光激发","authors":"B. Raffel, J. Wolfrum","doi":"10.1155/1990/93626","DOIUrl":null,"url":null,"abstract":"An investigation is presented of the transient vibrational excitation of O3 in the collision dominated \nregime initiated by pulsed CO2-laser radiation. IR-UV-double resonance experiments and measurements \nof the absorbance for the CO2-laser lines 9P18, 20, and 22 were carried out. Mixtures of O3 (p=17 mbar) \nwith 02 were investigated at pressures of 160 mbar ≤Pmixt≤1200 mbar and laser fluences of 0.10 J/cm2≤Fin< 2 J/cm2 \n. The results are interpreted by numerical simulations in terms of a comprehensive \nexcitation/relaxation model based upon SSH-theory. Concerning the evolution of the excitation, simulated \ntransients of the UV-absorbance compare well with the corresponding observed signals. The \nsaturation of the absorbing O3-transitions is demonstrated by the measured fluence dependence of the \nabsorption coefficient at the laser wavelengths. The extent of the 03-excitation can be deduced according \nto the model from the maximum vibrational temperature Tm reached in the v1- and v3-oscillators. Tm \naccessible via the UV-transients and also via the absorbed laser energy in the case of slow relaxation at 160 \n160mbar≤Pmixt≤340 mbar. In this range both techniques result in the same values for Tm. The experimental \nand the corresponding simulated Tm depend exponentially on the laser fluence (Tm =const . F¯in0.3) \nprovided Tm>400K being also confirmed up to Pmixt=1200 mbar by the observed UV-transients.","PeriodicalId":296295,"journal":{"name":"Laser Chemistry","volume":"35 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Pulsed Co2-Laser Excitation of 03/02 Mixtures at Pressures From 0.16 to 1.20 Bar\",\"authors\":\"B. Raffel, J. Wolfrum\",\"doi\":\"10.1155/1990/93626\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An investigation is presented of the transient vibrational excitation of O3 in the collision dominated \\nregime initiated by pulsed CO2-laser radiation. IR-UV-double resonance experiments and measurements \\nof the absorbance for the CO2-laser lines 9P18, 20, and 22 were carried out. Mixtures of O3 (p=17 mbar) \\nwith 02 were investigated at pressures of 160 mbar ≤Pmixt≤1200 mbar and laser fluences of 0.10 J/cm2≤Fin< 2 J/cm2 \\n. The results are interpreted by numerical simulations in terms of a comprehensive \\nexcitation/relaxation model based upon SSH-theory. Concerning the evolution of the excitation, simulated \\ntransients of the UV-absorbance compare well with the corresponding observed signals. The \\nsaturation of the absorbing O3-transitions is demonstrated by the measured fluence dependence of the \\nabsorption coefficient at the laser wavelengths. The extent of the 03-excitation can be deduced according \\nto the model from the maximum vibrational temperature Tm reached in the v1- and v3-oscillators. Tm \\naccessible via the UV-transients and also via the absorbed laser energy in the case of slow relaxation at 160 \\n160mbar≤Pmixt≤340 mbar. In this range both techniques result in the same values for Tm. The experimental \\nand the corresponding simulated Tm depend exponentially on the laser fluence (Tm =const . F¯in0.3) \\nprovided Tm>400K being also confirmed up to Pmixt=1200 mbar by the observed UV-transients.\",\"PeriodicalId\":296295,\"journal\":{\"name\":\"Laser Chemistry\",\"volume\":\"35 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Laser Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/1990/93626\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laser Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/1990/93626","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Pulsed Co2-Laser Excitation of 03/02 Mixtures at Pressures From 0.16 to 1.20 Bar
An investigation is presented of the transient vibrational excitation of O3 in the collision dominated
regime initiated by pulsed CO2-laser radiation. IR-UV-double resonance experiments and measurements
of the absorbance for the CO2-laser lines 9P18, 20, and 22 were carried out. Mixtures of O3 (p=17 mbar)
with 02 were investigated at pressures of 160 mbar ≤Pmixt≤1200 mbar and laser fluences of 0.10 J/cm2≤Fin< 2 J/cm2
. The results are interpreted by numerical simulations in terms of a comprehensive
excitation/relaxation model based upon SSH-theory. Concerning the evolution of the excitation, simulated
transients of the UV-absorbance compare well with the corresponding observed signals. The
saturation of the absorbing O3-transitions is demonstrated by the measured fluence dependence of the
absorption coefficient at the laser wavelengths. The extent of the 03-excitation can be deduced according
to the model from the maximum vibrational temperature Tm reached in the v1- and v3-oscillators. Tm
accessible via the UV-transients and also via the absorbed laser energy in the case of slow relaxation at 160
160mbar≤Pmixt≤340 mbar. In this range both techniques result in the same values for Tm. The experimental
and the corresponding simulated Tm depend exponentially on the laser fluence (Tm =const . F¯in0.3)
provided Tm>400K being also confirmed up to Pmixt=1200 mbar by the observed UV-transients.