Color center laser kinetic spectroscopy

dc.contributor.advisorCurl, Robert F., Jr.en_US
dc.creatorStephens, James Wesleyen_US
dc.date.accessioned2009-06-04T00:39:58Zen_US
dc.date.available2009-06-04T00:39:58Zen_US
dc.date.issued1989en_US
dc.description.abstractHigh resolution color center laser kinetic spectroscopy has been used to study the kinetics and spectroscopy of free radicals. The radicals are produced in a flowing system by the excimer laser photolysis of stable precursors. The transient infrared absorptions of the radicals are monitored with better than 1 $\mu$s time resolution. Spectra of the ethynyl radical (C$\sb2$H), produced by photolysis of acetylene, were collected between 3000 and 3600 cm$\sp{-1}$ with a goal of identifying the CH stretching fundamental of the molecule. A number of new bands of C$\sb2$H and its carbon-13 analogue ($\sp{13}$C$\sp{13}$CH) were observed and rotationally analyzed. These bands include three C$\sb2$H bands of $\sp2\Sigma\sp+$ + $\gets$ $\sp2\Sigma\sp+$ symmetry, one C$\sb2$H band of $\sp2\Pi$ $\gets$ $\sp2\Pi$ symmetry, three $\sp{13}$C$\sb2$H bands of $\sp2\Sigma\sp+$ + $\gets$ $\sp2\Sigma\sp+$ symmetry, and one $\sp{13}$C$\sb2$H band of $\sp2\Pi$ $\gets$ $\sp2\Pi$ symmetry. A number of $\sp{13}$C analogues of $\sp{12}$C$\sb2$H bands were identified. However, no conclusive assignment has been made for the CH stretch. Two tentative assignment schemes are given for several of the bands. The kinetics of the C$\sb2$H + O$\sb2$ reaction were studied with a goal of determining the reaction products. OH radicals were determined to be a minor product of this reaction. Experiments designed to determine the relative importance of the hydrogen atom producing channel were inconclusive. In other kinetic studies, a high temperature furnace was constructed to determine the temperature dependences of the product channels of the NH$\sb2$ + NO reaction. The reaction was initiated by the photolysis of NH$\sb3$ in the presence of NO. The branching ratios of the OH and H$\sb2$O producing channels were determined at 26, 400, 700, and 925$\sp\circ$C by comparison of the increase in OH and H$\sb2$O absorption signals with the decrease in an NH$\sb3$ absorption signal. Branching ratios were calculated from the raw signals by using the infrared cross sections of the molecules, measured in separate experiments. The branching ratio of the OH channel is 14% at room temperature and increases to 25% at 925$\sp\circ$C. The total of the two channels (OH plus H$\sb2$O) accounts for 100% of the reaction at room temperature; however, this number drops to about 80% for higher temperatures, possibly indicating the onset of another channel.en_US
dc.format.extent187 p.en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.callnoThesis Chem. 1989 Stephensen_US
dc.identifier.citationStephens, James Wesley. "Color center laser kinetic spectroscopy." (1989) Diss., Rice University. <a href="https://hdl.handle.net/1911/16300">https://hdl.handle.net/1911/16300</a>.en_US
dc.identifier.urihttps://hdl.handle.net/1911/16300en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.subjectPhysical chemistryen_US
dc.titleColor center laser kinetic spectroscopyen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentChemistryen_US
thesis.degree.disciplineNatural Sciencesen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophyen_US
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