Thesis (Ph. D.)--University of Washington, 1998. / Vita. Includes bibliographical references (leaves [169]-179).

Thesis (Ph. D., Biological and Agricultural Engineering)--University of Idaho, May 2008. / Major professor: Dev S. Shrestha. Includes bibliographical references. Also available online (PDF file) by subscription or by purchasing the individual file.

From introduction: The Fluorescence Excitation Spectrum or anthracene is known to vary considerably with the age and condition or the crystal. This thesis represents an attempt to improve the understanding of these variations. To put the problem on a quantitative basis it was found necessary to know both the ultraviolet reflection and absorption spectra. Reports of the reflection spectrum appear to have been confined to the case of polarised incident light. In addition the reflectivity measurements are always reported for a freshly cleaved surface. For these reasons the reflectivity of anthracene for various conditions of the reflecting surface was measured with unpolarised light. These varying reflectivities were used to further knowledge of the chemical processes at the crystal surface, as well as being used directly in the calculation of fluorescence excitation spectra. Reflection spectra with a- and b- crystallographic axis polarisations were also obtained. Since such spectra are reported in the literature it was possible, by comparison, to conclude that the experimental methods used in this thesis yielded valid results. The polarised measurements were used to obtain optical constants for the crystal. In the interests of readability most of the complicated process of converting the reflectivities to optical constants is dealt with in three appendices to the thesis.

<p> In Part I of this thesis, the design, construction, and calibration of a twenty-one foot off-plane Eagle vacuum spectrograph, a Lyman source, and predispersion unit are described.</p> <p> In Part II, the results of an investigation of the electronic absorption spectra of the cyanogen halides, obtained with the apparatus described in Part I, are given. Several electronic absorption systems have been observed for each of the cyanogen halides. These have been correlated and assigned to electronic transitions. Vibrational analyses have been made and the excited state dimensions have been determined by a quantitative application of the Franck-Condon principle for two absorption systems of each of the cyanogen halides.</p> / Thesis / Doctor of Philosophy (PhD)

A paucity of literature exists on the Independent System analysis of adjacent, parallel transition dipoles. Applying this theory and certain spectral information semiemperical calculations were made to predict absorption profiles and band intensities. To aid in the assignment of the 7*+7 absorption bands it was necessary to obtain the vacuum ultraviolet spectra of cyclohexane and cyclohexene. Because the spectra of these molecules contained sharp, atomic-like absorption bands a Rydberg series could be fitted to certain absorptions, thus the determination of their ionization potentials. Using Independent System analysis profiles and intensities of 7*+q-- absorption bands ins 'several methyl substituted 1,4- cyclohexadienes and isotetralin were predicted where general agreement was found with observed experimental spectra.

Indiana University-Purdue University Indianapolis (IUPUI) / In the area of forensic chemistry, improved or new analysis methods are continually being investigated. One common and powerful technique used in forensic chemistry is wall-coated open-tubular column (WCOT) gas chromatography with electron ionization single quadrupole mass spectrometry (GC-MS). Improvements to and effectiveness of alternatives to this instrumental platform were explored in an array of parallel inquiries. The areas studied included the column for the chromatographic separation, the universal detection method employed, and the fragmentation method used to enhance molecular identification. Superfine-micropacked capillary (SFµPC) columns may provide an alternative to commercial packed GC columns and WCOT GC columns that combines the benefits of the larger sample capacity of packed columns and the benefits of the excellent separation capabilities and mass spectrometry (MS) flow rate compatibility of WCOT columns. SFµPC columns suffer from high inlet pressure requirements and prior reported work has required specialized instrumentation for their use. Fabrication of and chromatography with SFµPC GC columns was successfully achieved with typical GC-MS instrumentation and within the flow rate limit of a MS. Additionally, the use of higher viscosity carrier gasses was demonstrated to reduce the required inlet pressure for SFµPC GC columns. Recently, a new vacuum ultraviolet spectrometer (VUV) universal detector has been commercialized for GC. The ability of VUV detectors to acquire absorbance spectra from 125 nm to 430 nm poses a potential alternative to MS. As such, GC-VUV provides an exciting potential alternative approach to achieving excellent quantitative and qualitative analysis across a wide range of analytes. The performance of VUV and MS detectors for forensic analysis in terms of quantitative and qualitative analysis was compared. Analysis of alkylbenzenes in ignitable liquids was explored, which can be important evidence from suspected arson fires and are difficult to differentiate with MS. The VUV detector was found to have superior specificity and comparable sensitivity to the MS detector in scan mode. Addition of thermolysis (Th) as an orthogonal fragmentation pathway provides the opportunity to increase the differences between MS fragmentation patterns. Fragmentation has been widely established to aid in identification of molecules with MS by providing characteristic fragments at characteristic relative abundances. However, molecules with very similar structures do not result in sizable spectral differences in all cases with typical MS fragmentation techniques. A series of Th units were fabricated and integrated into GC-Th-MS instruments. Th-MS was conducted with the thermally labile nitrate esters across a range of instrumentation and thermal conditions.

An automated continuous flow analysis for milk protein utilizing ultraviolet spectroscopy resulted in a correlation coefficient of 0.972 and a standard estimate of error of 0.082 percent protein when 30 samples were compared with the acid orange 12 dye binding method. Milk was solubilized in 95-105 volumes of acetic acid using the Technicon Auto Analyzer II and measured for absorbance at 274 nanometers. No deviation from the standard method due to mastitis and varying milk fat concentration was observed. A theoretical model indicated a possible standard estimate of error 0.059 percent protein due to inter- and intra-breed variation in milk protein fraction distribution. Potassium dichromate and other preservatives interfered with the results.

Thesis (MSc (Physics))--University of Stellenbosch, 2005. / A tunable vacuum ultra-violet (VUV) laser source was recently developed for VUV spectroscopy using state selective excitation and total fluorescence detection. The VUV laser source makes use of a four-wave mixing process to provide tunable VUV radiation for the electronic excitation of the molecules. The theory of four-wave mixing, with the emphasis on parameters that are important for our experimental setup to generate efficient tunable VUV radiation is discussed. The experimental setup, and in particular the metal vapor heat-pipe, which provides Mg vapor as the nonlinear medium, is described. New diagnostic equipment described in this work was added to the experimental setup. This equipment was characterized and utilized together with the existing setup. The additional diagnostic equipment introduced enabled us to measure the tunable VUV output of the source (using a VUV monochromator), making it possible to significantly improve the efficiency of the existing tunable VUV laser source.

Thesis (PhD)--Stellenbosch University, 2003. / ENGLISH ABSTRACT: A tunable narrow-bandwidth laser source combined with a supersonic gas jet as sample is wellsuited for obtaining high-resolution spectra of cold isolated molecules and complexes. In the present study such a laser source in the vacuum ultraviolet was applied to the spectroscopic investigation of rare carbon monoxide (CO) isotopomers and CO-noble gas van der Waals complexes in supersonic gas pulses seeded with natural CO gas. Tunable coherent vacuum ultraviolet radiation was generated by two-photon resonant fourwave sum-frequency mixing of two pulsed dye laser beams in a magnesium vapour medium. Laser induced fluorescence excitation spectra of the A(v'=3)-X(v"=0) vibronic band of CO molecules in a noble gas (neon or argon) jet were obtained by measuring the total undispersed fluorescence from the irradiated sample volume in dependence of the excitation wavelength. The dynamics of the flow-cooling process in the supersonic jet were investigated and the experimental parameters optimised using the rotational temperature of 12C160as determined from rotational line intensities. Rotational temperatures as low as 2 ± I K were observed. Spectroscopic detection of the rare 12C170and 12C180isotopomers was facilitated by the low rotational temperature and high spectral resolution. Six rotational lines of 12C170and four of 12C180were detected in the A(v'=3)-X(v"=0) vibronic band. This demonstrates the low detection limit (circa 3 parts per million) obtained in the experiment. The line wavelengths were determined to an accuracy of 0.2 pm using the well-documented 12C160and 13C160lines for calibration. The spectral results on 12C170are, to our knowledge, the first rotationally resolved laboratory measurements published on the A-X band of this isotopomer. Accurate wavelength data of the stable isotopomers of CO is of importance in the interpretation of astrophysical observations of CO in the interstellar medium. The newly determined 12C170wavelengths were successfully applied to a recent problem in astrophysics (Astrophys. J. Lett. 2003). The conditions in a supersonic jet facilitate the study of weakly bound van der Waals complexes, of which CO-noble gas complexes are prototypes. However, there is no experimental data available on the electronic excitation spectra of the CO-noble gas complexes, lying in the vacuum ultraviolet region. In the present experiment evidence of extensive complexation of the CO in the noble gas jet has been found, but in the spectral region around the A(v'=3)-X(v"=O) band of CO no distinct spectral features that could be associated with these complexes were observed. Having considered the existing knowledge on CO and CO-noble gas complexes and experimental studies on the excitation and dissociation dynamics of Iz-noble gas complexes, we regard complex induced inter-system crossing or electronic predissociation as the most likely causes for these observations. The results on the rare CO isotopomers demonstrate the potential of our experimental setup for high-resolution, isotope and state selective spectroscopy in the vacuum ultraviolet with a high sensitivity for fluorescent species. The availability of the now well-characterised experimental setup in our laboratory opens the way for further investigation of molecular or complex species with spectroscopic features in the vacuum ultraviolet region. / AFRIKAANSE OPSOMMING: Vakuum ultraviolet laser spektroskopie van CO molekules in 'n supersoniese gasstraal: 'n Afstembare smal bandwydte laserbron en 'n supersoniese gasstraal as monster is 'n geskikte kombinasie vir hoë-resolusie spektroskopie van geïsoleerde afgekoelde molekules en komplekse. In hierdie studie is so 'n laserbron in die vakuum ultraviolet gebruik in die spektroskopiese ondersoek van skaars koolstofmonoksied (CO) isotopomere en CO-edelgas van der Waals komplekse in supersoniese gaspulse wat 'n klein persentasie natuurlike CO gas bevat. Afstembare koherente vakuum ultraviolet lig is verkry deur twee-foton resonante vier-golf som-frekwensie vermenging van twee gepulseerde kleurstoflaserbundels in 'n magnesiumdamp medium. Laser-geïnduseerde fluoressensie opwekkingspektra van die A(v'=3)-X(v"=0) vibroniese band van die CO molekules in die edelgasstraal (neon of argon) is uitgemeet deur die totale fluoressensie van die beligte gasmonster, sonder golflengteskeiding, te meet as funksie van die opwekkingsgolflengte. Die dinamika van die vloeiverkoelingsproses in die supersoniese gasstraal is ondersoek en die eksperimentele parameters geoptimeer deur gebruik te maak van die rotasionele temperatuur van 12Cl60 soos bepaal uit die intensiteitsverhoudings van die rotasielyne. Rotasionele temperature tot so laag as 2 ± 1 K is waargeneem. Spektroskopiese waarneming van die skaars 12C170 and 12Cl80 isotopomere is moontlik gemaak deur die lae rotasionele temperatuur en die hoë spektrale resolusie. Ses rotasielyne van 12C170 en vier van 12C180 is waargeneem in die A(v'=3)-X(v"=0) vibroniese band. Dit demonstreer die lae deteksielimiet (ongeveer 3 dele per miljoen) wat bereik kon word. Die golflengtes van die lyne is bepaal met 'n akkuraatheid van 0.2 pm deur die bekende lyne van 12C160en 13C160vir kalibrasie te gebruik. Die resultate ten opsigte van 12C170 is sover vasgestel kon word die eerste rotasioneel-opgeloste laboratorium metings van die A-X band van hierdie isotopomeer. Akkurate golflengte data vir die stabiele CO isotopomere is van belang vir die interpretasie van die astrofisiese waarnemings van CO in die interstellêre medium. Die nuwe 12C170 golflengtes is suksesvol aangewend in die oplossing van 'n onlangse interpretasieprobleem in astrofisika (Astrophys. J. Lett. 2003). Die toestande in 'n supersoniese gasstraal maak die bestudering van swak-gebonde van der Waals komplekse moontlik. Hoewel CO-edelgas van der Waals komplekse as prototipes beskou word, is daar geen eksperimentele data beskikbaar oor die elektroniese opwekkingspektra van hierdie spesies, wat in die vakuum ultraviolet gebied lê, nie. In hierdie studie is daar eksperimentele getuienis gevind vir uitgebreide kompleksering van CO in die edelgasstraal, maar in die spektraalgebied rondom die A(v'=3)-X(v"=O) band van CO is geen duidelike spektrale kenmerke wat met hierdie komplekse geassosieer kan word, waargeneem nie. Na oorweging van die bestaande kennins oor CO en CO-edelgas komplekse en eksperimentele studies oor die opwekking en dissosiasie-dinamika van Iz-edelgas komplekse, beskou ons kompleksgeïnduseerde intersisteemoorgange of elektroniese predissosiasie as die waarskynlikste redes vir hierdie waarnemings. Die resultate oor die skaars CO isotopomere toon die potensiaal van ons eksperimentele opstelling vir hoë-resolusie, isotoop- en toestandselektiewe spektroskopie in die vakuum ultraviolet met uitstekende sensitiwiteit vir fluoresserende spesies. Die beskikbaarheid van hierdie nou deeglik gekarakteriseerde eksperimentele opstelling in ons laboratorium maak verdere ondersoek na molekulêre of kompleks-spesies met spektroskopiese kenmerke in die vakuum ultraviolet moontlik.

Inductively-Coupled Plasma Optical Emission Spectrometry (ICP-OES) is evaluated as a method for the selective determination of several non-metals which emit light in the Vacuum Ultraviolet (VUV) region of the spectrum. In this study, emphasis is placed on those elements which are totally unobservable with standard techniques or have very weak lines in the UV-VIS region of the spectrum. The sensitivity and accuracy of the apparatus and methods devised allows the determination of empirical formulas of gas chromatographic effluents. The results of this study indicate that the background emission of the ICP in the VUV is low level and nearly constant over the entire spectral region investigated (125 - 185 nm.). Promising analytical lines for oxygen, nitrogen, chlorine, bromine, and carbon are also observed in this region. A progression of four experimental configurations were constructed, employing a purged optical path and a unique coolant tube design. The last of these configurations has the capability of spatial resolution of individual portions of the discharge so that emission maps and profiles could be constructed. The results of the maps generated indicate that the region of highest emission intensity is always centered in the discharge. However, the vertical position of this region is found to be dependent upon r.f. power and argon flow rates. Detection limits in the low nanogram region are observed for each non-metal. The dynamic range for each element is in excess of 10⁴ and the selectivity ratio versus carbon is above 100 in each case. A method was developed for determining the elemental composition of the effluents of a GC. Using internal standards, the method is independent of the weight of each component eluted thus sampling errors are eliminated. The average relative errors in multielement analysis are 0.89%, 0.75%, 2.1%, 0.55%, and 0.64% for the percent carbon, oxygen, nitrogen, chlorine, and bromine, respectively.