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Sediment Bound Trace Metals in the White Rock Creek Watershed, Dallas and Collin Counties (open access)

Sediment Bound Trace Metals in the White Rock Creek Watershed, Dallas and Collin Counties

Areas were sampled in the White Rock Creek Watershed to examine sediment bound trace metal distributions and sorption relationships. A Kruskal-Wallis AOV found significant among area differences for most metals, and SNK-like multiple comparisons were used to group these areas. Kruskal-Wallis AOVs similarly found among area differences for sediment components that bind trace metals (Fe and Mn oxides and organic carbon) and physicochemical conditions that influence metal sorption (particle size and pH). Multiple correlation found numerous relationships among trace metals, sediment components, and physicochemical conditions. Statistical relationships indicate that metal partitioning to various sorption factors is metal specific. White Rock Creek Watershed trace metal concentrations are comparable to those in many urban watersheds.
Date: May 1990
Creator: Combest, Kyle B. (Kyle Bryan)
System: The UNT Digital Library
The Effect of Nine Diet and Water Combinations on the Culture Health of Ceriodaphnia Dubia (open access)

The Effect of Nine Diet and Water Combinations on the Culture Health of Ceriodaphnia Dubia

Culture health of Ceriodaphnia dubia was evaluated for organisms cultured using all combinations of three foods and three waters. Criteria used to assess health of cultures included adult and neonate weights, time required to produce first broods, neonate production, adult survival, and resistance to hexavalent chromium. Diet/water combinations which produced the most neonates were not found to produce adults which were more resistant to chromium than those which produced fewer neonates. Of those evaluated, a diet of Selenastrum capricornutum and a yeast-trout chow-cereal leaf mixture was best for culturing and testing Ceriodaphnia. The best synthetic water tested was a mixture of nine parts reconstituted hard water and one part bottled mineral water.
Date: May 1990
Creator: Patterson, Paul W. (Paul William)
System: The UNT Digital Library
Assessment of Functional Communication Skills in Institutionalized and Non-Institutionalized Elderly Subjects Using the Spontaneous Speech and Auditory Comprehension Subtests of the Western Aphasia Battery (open access)

Assessment of Functional Communication Skills in Institutionalized and Non-Institutionalized Elderly Subjects Using the Spontaneous Speech and Auditory Comprehension Subtests of the Western Aphasia Battery

The purpose of this study was to determine if there is a difference in functional communication skills between elderly persons in nursing homes and those living independently in the community. Thirty non-institutionalized elderly subjects were given the Western Aphasia Battery (WAB) screening tool. These scores were compared to WAB screening scores obtained from 20 institutionalized subjects. The difference between these scores was statistically significant. The institutionalized subjects' scores were also correlated with a Facilitators Evaluation of Communication Skills (FECS) inventory. Results showed a moderate correlation between the institutionalized subjects' WAB screening score and their FECS rating. The benefits of a screening tool for elderly populations are discussed.
Date: August 1990
Creator: Cutshaw, Laura M. (Laura Marie)
System: The UNT Digital Library
Natural Innocence in "Adventures of Huckleberry Finn", the Nick Adams Stories, and "The Old Man and the Sea" (open access)

Natural Innocence in "Adventures of Huckleberry Finn", the Nick Adams Stories, and "The Old Man and the Sea"

Hemingway claims in Green Hills of Africa that "all modern American literature comes from one book by Mark Twain called Huckleberry Finn." If this basic idea is applied to his own work, elements of Adventures of Huckleberry Finn appear in some of Hemingway's Nick Adams stories and his novel The Old Man and the Sea. All major characters and several minor characters in these works share the quality of natural innocence, composed of their primitivism, sensibility, and active morality. Hemingway's Nick, Santiago, and Manolin, and Twain's Huck Finn and Jim reflect their authors' similar backgrounds and experiences and themselves come from similar environments. These environments are directly related to their continued possession and expression of their natural innocence.
Date: May 1990
Creator: Hall, Robert L. (Robert Lee), 1956-
System: The UNT Digital Library
Syntheses and Structures of Substituted Polycyclic Molecules and Analysis of the Two-Dimensional NMR Spectrum of Thiele's Ester (open access)

Syntheses and Structures of Substituted Polycyclic Molecules and Analysis of the Two-Dimensional NMR Spectrum of Thiele's Ester

Diels-Alder cycloaddition of methylcyclopentadienes to 2,5-dibromo-p-benzoquinone was performed. A single, isomerically pure cycloadduct was isolated, whose structure was assigned via analysis of its 1-D and 2-D NMR spectra. Diels-Alder cycloaddition of methylcyclopentadienes to 2 -methoxy-p-benzoquinone was performed. A single, isomerically pure cycloadduct was isolated, whose structure was assigned via analysis of the 1-D and 2-D NMR spectra of this cycloadduct and its reduction product obtained via stereo-specific reduction with sodium borohydride in the presence of cerous chloride. The structure of Thiele's ester was assigned via analysis of its 1-D and 2-D NMR spectra.
Date: May 1990
Creator: Lu, Shao-Po
System: The UNT Digital Library
Factors Relating to Upper Level Employee Support for Organizational Redesign (open access)

Factors Relating to Upper Level Employee Support for Organizational Redesign

Successful implementation of organizational redesign depends on the support of employees at all levels of the organization. This study looked at some of the factors that are related to employee support for organizational redesign. Subjects (82 support staff members of a small manufacturing plant undergoing organizational change) were administered a survey which measured employee perceptions about the change management process and the disruption the change caused to their daily routine. Eleven variables were assessed as independent variables in terms of their relationship to the dependent variable which was employee support of the organizational change. All eleven variables were significantly related to the dependent variable. The implications of these results and issues for further research was discussed.
Date: August 1990
Creator: Street, Amy
System: The UNT Digital Library
Observation by flow sup 1 H NMR and dimerization kinetics and products of reactive ortho-quinodimethanes and benzocyclobutadiene (open access)

Observation by flow sup 1 H NMR and dimerization kinetics and products of reactive ortho-quinodimethanes and benzocyclobutadiene

The reactive o-quinodimethanes, 1,2-dimethylene-1,2-dihydronaphthalene (9) and o-xylylene (1) were observed by flow {sup 1}H NMR spectroscopy at room temperature. The {sup 1}H NMR spectrum of 9 was obtained in the absence of precursor and dimers. However, the {sup 1}H NMR spectrum of the more reactive 1, generated in a similar manner from (o-((trimethylsilyl)methyl)benzyl)trimethylammonium iodide (5.) could be obtained only in the presence of its stable (4 + 2) and (4 + 4) dimers. The dimerization kinetics of 3-methyl- (5{prime}), 3,6-dimethyl- (11), 3-isopropyl- (12), and 3,6-diisoproply-1,2-xylylene (13) in acetonitrile (CH{sub 3}CN) were studied by stopped-flow UV-visible spectroscopy. Fluoride ion induced 1,2-elimination from 2-elimination from 2-trimethylsilylbenzocyclobutenyl-1 mesylate (26) was used to generate the reactive molecule benzocyclobutadiene (1{prime}) in CD{sub 3}CN, which was observed by flow {sup 1}H NMR spectroscopy at room temperature. The {sup 1}H NMR spectrum (in CD{sub 3}CN) of 1,2-dimethylene-1,2-dihydrothiophene (1{double prime}), obtained by fluoride ion induced 1,4-elimination from 3-(trimethylammoniummethyl)-2-(trimethylsilylmethyl)thiophene iodine was observed by flow {sup 1}H NMR spectroscopy at room temperature. The dimerization rate of 1{double prime} in CH{sub 3}CN, generated in the same manner, was measured by UV-visible spectroscopy. 166 refs., 7 figs., 7 tabs.
Date: September 21, 1990
Creator: Fischer, David
System: The UNT Digital Library
Magnetic and thermal properties of high Tc superconductors (open access)

Magnetic and thermal properties of high Tc superconductors

Measurements of the normal state magnetic susceptibility {chi}(T) of YBa{sub 2}Cu{sub 3}O{sub 7}, Bi{sub 1.8}Pb{sub 0.2}Sr{sub 2}CaCu{sub 2}O{sub 8+{delta}}, and Bi{sub 2{minus}x}Pb{sub x}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10+{delta}} (x = 0.2 and 0.25) were carried out. All {chi}(T) data show negative curvature below {approximately}2{Tc}. The data for YBa{sub 2}Cu{sub 3}O{sub 7} are in excellent agreement with a new calculation of the superconducting fluctuation diamagnetism. From the analysis, we infer s-wave pairing and microscopic parameters are obtained. For {chi}(T) of YBa{sub 2}Cu{sub 3}O{sub 7}, part of the negative curvature is inferred to arise from the normal state background. We find a strong temperature dependent anisotropy {delta}{chi} {equivalent to} {chi}{sub c} {minus} {chi}{sub ab} and estimate the normal state spin contributions to {chi}(T). The heat capacity C(T) of YBa{sub 2}Cu{sub 3}O{sub 7} is reported for 0.4 K < T < 400 K in zero and 70 kG magnetic fields. In addition to the feature associated with the onset of the superconductivity at {Tc}, two anomalies in C(T) were observed near 74 K and 330 K, with another possible anomaly near 102 K; the temperatures at which they occur correlate with anomalies in {chi}(T) and ultransonic measurements. The occurrence of the anomaly at {approx …
Date: September 21, 1990
Creator: Lee, Wonchoon
System: The UNT Digital Library
A Search for Thermal Isomerization of Olefins to Carbenes: Thermal Generations of the Silicon-Nitrogen Double Bond (open access)

A Search for Thermal Isomerization of Olefins to Carbenes: Thermal Generations of the Silicon-Nitrogen Double Bond

The first part of this thesis will search for the thermal isomerization of olefins to carbenes which is predicted to be a high energy process by calculations and has only been observed in a few strained olefins. The possibility of thermal isomerization of simple olefins to carbenes will be explored. Substitution of a silyl group on the double bond of an olefin allows a potential intermediate which has a {beta}-radical to the silyl group during the cis-trans isomerization. The effects of a trimethylsilyl group on this isomerization are the subject of this study. The second part of this thesis will include the generation and chemistry of intermediates containing a silicon-nitrogen double bond. The isomerization of parent silanimine to the aminosilylene was calculated to be a high energy process. New approaches to the silicon-nitrogen double bond will also be presented. 92 refs., 12 figs., 11 tabs.
Date: September 21, 1990
Creator: Zhang, Xianping
System: The UNT Digital Library
Physical metallurgy and magnetic behavior of Cd stabilized bcc (beta)Gd alloys (open access)

Physical metallurgy and magnetic behavior of Cd stabilized bcc (beta)Gd alloys

As a continuation of the research on bcc Gd-Mg alloy system by Herchenroeder and Gschneidner, the metastable bcc Gd-Cd alloys were studied with the emphasis on their metallurgical and magnetic properties. An essentially single phase alloy could be retained for Cd concentrations from 15 at. % Cd to 19 at. % Cd, which is in the vicinity of the eutectoid composition of {beta}Gd in the Gd-Cd system. The lattice constants obtained for these alloys were used to determine the lattice constant of pure bcc Gd by extrapolation to 0 at. % Cd. Good agreement between this extrapolated value and that obtained from Gd-Mg alloys by using the same method suggested the validity of such extrapolation method. Thermal stability of these metastable bcc Gd-Cd alloys was examined by using differential thermal analysis (DTA).
Date: September 21, 1990
Creator: Tang. Jinke
System: The UNT Digital Library
A reciprocal space approach for locating symmetry elements in Patterson superposition maps (open access)

A reciprocal space approach for locating symmetry elements in Patterson superposition maps

A method for determining the location and possible existence of symmetry elements in Patterson superposition maps has been developed. A comparison of the original superposition map and a superposition map operated on by the symmetry element gives possible translations to the location of the symmetry element. A reciprocal space approach using structure factor-like quantities obtained from the Fourier transform of the superposition function is then used to determine the best'' location of the symmetry element. Constraints based upon the space group requirements are also used as a check on the locations. The locations of the symmetry elements are used to modify the Fourier transform coefficients of the superposition function to give an approximation of the structure factors, which are then refined using the EG relation. The analysis of several compounds using this method is presented. Reciprocal space techniques for locating multiple images in the superposition function are also presented, along with methods to remove the effect of multiple images in the Fourier transform coefficients of the superposition map. In addition, crystallographic studies of the extended chain structure of (NHC{sub 5}H{sub 5})SbI{sub 4} and of the twinning method of the orthorhombic form of the high-{Tc} superconductor YBa{sub 2}Cu{sub 3}O{sub 7-x} are …
Date: September 21, 1990
Creator: Hendrixson, Ton
System: The UNT Digital Library
Optical properties and electronic structures of d- and f-electron metals and alloys, Ag-In, Ni-Cu, AuGa sub 2 , PtGa sub 2 ,. beta. prime -NiAl,. beta. prime -CoAl, CeSn sub 3 , and LaSn sub 3 (open access)

Optical properties and electronic structures of d- and f-electron metals and alloys, Ag-In, Ni-Cu, AuGa sub 2 , PtGa sub 2 ,. beta. prime -NiAl,. beta. prime -CoAl, CeSn sub 3 , and LaSn sub 3

Optical properties and electronic structures of disordered Ag{sub 1- x}In{sub x}(x = 0.0, 0.04, 0.08, 0.12) and Ni{sub 1-x}Cu{sub x} (x = 0.0, 0.1, 0.3, 0.4) alloys and ordered AuGa{sub 2}, PtGa{sub 2}, {beta}{prime}-NiAl, {beta}{prime}-CoAl, CeSn{sub 3}, and LaSn{sub 3} have been studied. The complex dielectric functions have been determined for Ag{sub 1-x}In{sub x}, Ni{sub 1-x}Cu{sub x}, AuGa{sub 2}, and PtGa{sub 2} in the 1.2--5.5 eV region and for CeSn{sub 3} and LaSn{sub 3} in the 1.5--4.5 eV region using spectroscopic ellipsometry. Self-consistent relativistic band calculations using the linearized-augmented-plane-wave method have been performed for AuGa{sub 2}, PtGa{sub 2}, {beta}{prime}-NiAl, {beta}{prime}-CoAl, CeSn{sub 3}, and LaSn{sub 3} to interpret the experimental optical spectra.
Date: October 17, 1990
Creator: Kim, Kwang Joo
System: The UNT Digital Library
Electrical Resistivity of Some Zintl Phase and the Precursors (open access)

Electrical Resistivity of Some Zintl Phase and the Precursors

Resistivity measurements have been performed for electric characterization of the compounds Ba{sub 5}Sb{sub 3} and Ba{sub 5}Sb{sub 3}Cl, both with the Mn{sub 5}Si{sub 3} structure type, along with Ca{sub 5}Bi{sub 3} and Ca{sub 5}Bi{sub 3}F, both with the {beta}-Yb{sub 5}Sb{sub 3} structure type. These measurements were taken as a function of temperature using the four probe method on pressed polycrystalline pellets of the compounds. A sealed apparatus was developed for containing these air-sensitive compounds throughout the experiments. By a simple electron count, one extra electron in both Ba{sub 5}Sb{sub 3} and Ca{sub 5}Bi{sub 3} should occupy a conduction band, giving these compounds a metallic character. In the cases of Ba{sub 5}Sb{sub 3}Cl and Ca{sub 5}Bi{sub 3}F, the extra electron should bond to the halide, both filling the valence band and giving rise to semiconducting character. Ca{sub 5}Bi{sub 3}, Ca{sub 5}Bi{sub 3}F, and Ba{sub 5}Sb{sub 3}Cl were found to comply with the electron count prediction. Ba{sub 5}Sb{sub 3}, however, was found to be a semiconductor (E{sub g} = 0.30 eV) with a larger band gap than its corresponding chloride (E{sub g} = 0.09 eV).
Date: September 21, 1990
Creator: Wolfe, Larry
System: The UNT Digital Library
High-resolution angle-resolved photoemission studies of high Tc superconductor Bi sub 2 Sr sub 2 CaCu sub 2 O sub 8 (open access)

High-resolution angle-resolved photoemission studies of high Tc superconductor Bi sub 2 Sr sub 2 CaCu sub 2 O sub 8

An angle-resolved photoemission study of the normal and superconducting states in Bi{sub 2}Sr{sub 2}CaCu{sub 2}O{sub 8} was performed. Measurements in the normal state show bands dispersing through the Fermi level from at least 350 meV below E{sub F}. The Fermi level crossings are consistant with local-density band calculation, including a point calculated to be of Bi-O character. Additional measurements were made where bands crossed the Fermi level between 100 and 250K, along with measurements on an adjacent Pt foil. The Fermi edges of both materials agree to within the noise. Below the Fermi level, the spectra show correlation effects on the form of an increased effective mass. The shape of the spectra can be explained by a lifetime-broadened photohole and secondary electrons. The effective inverse photohole lifetime is linear in energy. A superconducting gap has been measured at a number of points where there is density at the Fermi level in the normal state. By proper modeling, a gap of 24 meV was obtained for all these points, including points of Cu-O and Bi-O character respectively, according to band calculation. The lack of gap anisotropy in the basal plane suggests that pinning in this material is not d-wave pairing.
Date: September 21, 1990
Creator: Liu, Rong
System: The UNT Digital Library
Reactions of the excited state of polypyridyl chromium(III) ion (open access)

Reactions of the excited state of polypyridyl chromium(III) ion

There has been much recent interest in the photochemistry and photophysics of transition metal polypyridine complexes due to the possibility of their use in solar energy conversion systems. The excited state of these compounds are known to undergo useful electron transfer and energy transfer reactions. This work attempts to elucidate the mechanism of the quenching of *CrL{sub 3}{sup 3+} (where L = 2,2{prime}-bipyridine, 4,4{prime}-dimethyl-2,2{prime}-bipyridine, 1,10-phenanthroline, 5-chloro-1,10-phenanthroline, 5-methyl-1,10-phenanthroline) by oxalate ions in neutral pH. Evidence suggests an ion-pairing pre-equilibrium followed by rate limiting electron transfer to produce CrL{sub 3}{sup 2+} and CO{sub 2}{sup {minus}} can then react with ground state chromium(III) species to produce another mole of the reduced product or it can produce a secondary transient as in the case of phenanthroline and substituted phenanthroline complexes. The secondary transient reacts to produce CrL{sub 3}{sup 2+} in a subsequent reaction. 85 refs., 24 figs., 7 tabs.
Date: September 21, 1990
Creator: Steffan, Carl
System: The UNT Digital Library
Fundamental Investigations of Supported Monometallic and Bimetallic Catalysts by Proton Magnetic Resonance Spectroscopy (open access)

Fundamental Investigations of Supported Monometallic and Bimetallic Catalysts by Proton Magnetic Resonance Spectroscopy

Proton magnetic resonance spectroscopy, or nuclear magnetic resonance (NMR) of hydrogen, has been applied to investigate silica-supported Group VIII monometallic and Group VIII-Group IB bimetallic catalysts and alumina- and silica-supported platinum-rhenium bimetallic catalysts. Two adsorbed states of hydrogen, i.e., irreversible and reversible hydrogen, on the surfaces of monometallic Ru, Pt, and Cu particles and bimetallic Ru-Group Ib, Pt-Group Ib, and Pt-Re particles were observed directly via proton NMR. The same amounts of the irreversible hydrogen adsorbed on pure Ru catalysts were measured by both proton NMR and the volumetric technique. The electronic environments on surfaces of monometallic catalysts are sensitive to changes in metal dispersion, state of adsorbed hydrogen, and residual chlorine. Surface compositions for the Ru--Cu and Pt--Cu bimetallic catalysts were determined by NMR of adsorbed hydrogen. 297 refs., 96 figs., 19 tabs.
Date: September 21, 1990
Creator: Wu, Xi
System: The UNT Digital Library
Electrocatalysis of Anodic and Cathodic Oxygen-Transfer Reactions (open access)

Electrocatalysis of Anodic and Cathodic Oxygen-Transfer Reactions

The electrocatalysis of oxygen-transfer reactions is discussed in two parts. In Part I, the reduction of iodate (IO{sub 3}{sup {minus}}) is examined as an example of cathodic oxygen transfer. On oxide-covered Pt electrodes (PtO), a large cathodic current is observed in the presence of IO{sub 3}{sup {minus}} to coincide with the reduction of PtO. The total cathodic charge exceeds the amount required for reduction of PtO and IO{sub 3}{sup {minus}} to produce an adsorbed product. An electrocatalytic link between reduction of IO{sub 3}{sup {minus}} and reduction of PtO is indicated. In addition, on oxide-free Pt electrodes, the reduction of IO{sub 3}{sup {minus}} is determined to be sensitive to surface treatment. The electrocatalytic oxidation of CN{sup {minus}} is presented as an example of anodic oxygen transfer in Part II. The voltametric response of CN{sup {minus}} is virtually nonexistent at PbO{sub 2} electrodes. The response is significantly improved by doping PbO{sub 2} with Cu. Cyanide is also oxidized effectively at CuO-film electrodes. Copper is concluded to serve as an adsorption site for CN{sup {minus}}. It is proposed that an oxygen tunneling mechanism comparable to electron tunneling does not occur at the electrode-solution interface. The adsorption of CN{sup {minus}} is therefore considered to …
Date: September 21, 1990
Creator: Wels, Brian R.
System: The UNT Digital Library
Diffusion of trichloroethylene through the threaded joints of PVC (polyvinylchloride) pipe (open access)

Diffusion of trichloroethylene through the threaded joints of PVC (polyvinylchloride) pipe

The data engineers and scientists use to determine if the groundwater supply is contaminated are derived from analysis of samples taken largely from monitoring wells. For these data to be reliable several factors must be considered. One factor is the integrity of the monitoring well. In this project, emphasis has been placed on the potential impact on water quality caused by diffusion across the threaded joints of PVC pipe. In this study, the diffusion of trichloroethylene across several common types of threaded joints (i.e., square flush, modified ACME, modified ACME stub, and ACME) has been measured. Samples were obtained from the water inside the pipe sections and analyzed for trichloroethylene by gas chromatography. Breakthrough occurs within days of the samples being placed in the baths. The softened PVC joints of the pipes in the pure trichloroethylene split before the first sample interval of 1.5 weeks. The data show great variability in casting joints from the same manufacturer, and indicate a need for increased precision in the manufacturing of the PVC pipe joints. A one-dimensional diffusion model is used to determine an equivalent gap size through which the diffusion occurs. Flow rates through the threaded joints are calculated by using the …
Date: December 1, 1990
Creator: Jerome, Karen M.
System: The UNT Digital Library
Exclusive neutral strange particle production from double Pomeron exchange produced by proton-proton interactions at radical s = 62 GeV (open access)

Exclusive neutral strange particle production from double Pomeron exchange produced by proton-proton interactions at radical s = 62 GeV

Data are presented for the first time on exclusive Pomeron-Pomeron interactions which produce a neutral strange and neutral antistrange particle pair in a central system X. In this paper, the system, X, is identified as one of the following neutral combinations; K{sub s}{sup 0}K{sub s}{sup 0}, K{sub s}{sup 0}K{sup {plus minus}}{pi}{sup {minus plus}}, {Lambda}{sup 0}{bar {Lambda}}{sup 0}, {Lambda}{sup 0}{bar {Lambda}}{sup 0}*. These data were obtained in proton-proton collisions at {radical}s = 62 GeV at the CERN ISR. The triggering systems used to obtain these data are described, followed by a description of the data. The central system mass distributions are presented along with differential mass cross section estimates. A broad enhancement is seen in the K{sub s}{sup 0}K{sub s}{sup 0} system at a mass of 1.2 GeV, and is likely to have the quantum numbers J{sup PC} = 0{sup ++}. Total cross section estimates of 1.3 {plus minus} .64 {mu}b in the K{sub 2}{sup 0}K{sub s}{sup 0} system, . 44 {plus minus} .14 {mu}b in the K{sub s}{sup 0}K{sup {plus minus}}{pi}{sup {minus plus}} system, .20 {plus minus} .14 {mu}b in the {Lambda}{sup 0}{bar {Lambda}}{sup 0} system, and .13 {plus minus} .06 {mu}b in the {Lambda}{sup 0}{bar {Lambda}}{sup 0}* system are …
Date: September 21, 1990
Creator: Skeens, John
System: The UNT Digital Library
Kinetics and mechanisms of the reactions of alkyl radicals with oxygen and with complexes of Co(III), Ru(III), and Ni(III) (open access)

Kinetics and mechanisms of the reactions of alkyl radicals with oxygen and with complexes of Co(III), Ru(III), and Ni(III)

The kinetics of the reactions of C{sub 2}H{sub 5} radical with Co(NH{sub 3}){sub 5}X{sup 2+}, Ru(NH{sub 3}){sub 5}X{sup 2+}, and Co(dmgH){sub 2} (X) (Y) (X = Br, Cl, N{sub 3}, SCN; Y = H{sub 2}O, CH{sub 3}CN) complexes were studied using laser flash photolysis of ethylcobalt complexes. The kinetics were obtained by the kinetic probe method. Some relative rate constants were also determined by a competition method based on ethyl halide product ratios. The kinetics of colligation reactions of a series of alkyl radicals with {beta}-Ni(cyclam){sup 2+} were studied using flaser flash photolysis of alkylcobalt complexes. Again, the kinetics were obtained by employing the kinetic probe competition method. The kinetics of the unimolecular homolysis of a series of RNi(cyclam)H{sub 2}O{sup 2+} were studied. Activation parameters were obtained for the unimolecular homolysis of C{sub 2}H{sub 5}Ni(cyclam)H{sub 2}O{sup 2+}. Kinetic and thermodynamic data obtained from these reactions were compared with those for the {sigma}-bonded organometallic complexes. The kinetics of the unimolecular homolysis of a series of RNi(cyclam)H{sub 2}O{sup 2+} complexes were studied by monitoring the formation of the oxygen insertion product RO{sub 2}Ni(cyclam)H{sub 2}O{sup 2+}. The higher rate constants for the reactions of alkyl radicals with oxygen in solution, as compared with …
Date: October 8, 1990
Creator: Kelley, Douglas
System: The UNT Digital Library
Measurement of the Z-Boson Branching Fraction Into Hadrons Containing Bottom Quarks (open access)

Measurement of the Z-Boson Branching Fraction Into Hadrons Containing Bottom Quarks

We use the Mark II detector to study Z decays into bottom quark-anti-quark pairs, leading to the production of bottom hadrons. The Z bosons are formed in e{sup +}e{sup {minus}} annihilation at the SLC at center-of-mass energies between 89 and 93 GeV. We identify events containing semileptonic decays of bottom hadrons by detecting isolated leptons, i.e leptons with high transverse momenta relative to the nearest hadronic jet. Using isolated electrons and muons, we measure the B-hadron semileptonic branching ratio times the fraction of hadronic Z decays which contain bottom hadrons, B(B {yields} X{ell}{nu}){center dot}{Gamma}(Z {yields} b{bar b})/{Gamma}(Z {yields} had) = 0.025 {sub {minus}0.009}{sup +0.100} {plus minus} 0.005, where we have listed the statistical errors followed by the systematic error. Assuming B(B {yields} X(ell){nu}) = 11% {plus minus} 1%, we measure {Gamma}(Z {yields} b{bar b})/{Gamma}(Z {yields} had) = 0.23 {sub {minus}0.09}{sup +0.11}, in good agreement with the standard-model prediction of 0.22. We find {Gamma}(Z {yields} b{bar b}) = 0.40 {sub {minus}0.16}{sup +0.19} GeV. 83 refs., 34 figs., 19 tabs.
Date: September 1990
Creator: Kral, J. Frederic
System: The UNT Digital Library
Strangeonium spectroscopy at 11 GeV/c and Cherenkov Ring Imaging at the SLD (open access)

Strangeonium spectroscopy at 11 GeV/c and Cherenkov Ring Imaging at the SLD

This thesis is divided into two sections, which describe portions of the data acquisition system and online software for the Cherenkov Ring Imaging Detector (CRID) for the SLD, and analyses of several low cross section strangeonium channels in data from the LASS spectrometer. The CRID section includes a description of the data acquisition system, determination of the preamplifier gain, and development of an online pulse finding algorithm based on deconvolution. Deconvolution uses knowledge of the preamplifier impulse response to aid in pulse finding. The algorithm is fast and shows good single pulse resolution and excellent double pulse resolution in preliminary tests. The strangeonium analyses are based on data from a 4.1 event/nanobarn exposure of the LASS spectrometer in K{sup {minus}}p interactions at 11 GeV/c, and include studies of {Lambda}{eta}{pi}{sup {plus}}{pi}{sup {minus}}, {Lambda}{Kappa}*{Kappa}*, and {Lambda}{phi}{phi}.
Date: July 1990
Creator: Bienz, Timothy Lawrence
System: The UNT Digital Library
Application of Ultrasonic Guided Waves to the Characterization of Texture in Metal Sheets of Cubic and Hexagonal Crystallites (open access)

Application of Ultrasonic Guided Waves to the Characterization of Texture in Metal Sheets of Cubic and Hexagonal Crystallites

Ultrasonic techniques have recently been applied to the texture characterization in polycrystalline aggregates of hexagonal crystals. The basis of this application lies in the relations between the elastic constants {bar C}{sub ij} of the aggregates, which can be inferred from ultrasonic wave velocity measurements, and the orientation distribution coefficients. This communication present such relations for aggregates which possess orthotopic material symmetry and hexagonal crystal symmetry for Voigt, Reuss, and Hill averaging methods in a unified and concise representation.
Date: October 8, 1990
Creator: Li, Yan
System: The UNT Digital Library
Platinum(II) complexes as spectroscopic probes for biomolecules (open access)

Platinum(II) complexes as spectroscopic probes for biomolecules

The use of platinum(II) complexes as tags and probes for biomolecules is indeed advantageous for their reactivities can be selective for certain purposes through an interplay of mild reaction conditions and of the ligands bound to the platinum. The use of {sup 195}Pt NMR as a method of detecting platinum and its interactions with biomolecules was carried out with the simplest model of platinum(II) tagging to proteins. Variable-temperature {sup 195}Pt NMR spectroscopy proved useful in studying the stereodynamics of complex thioethers like methionine. The complex, Pt(trpy)Cl{sup +}, with its chromophore has a greater potential for probing proteins. It is a noninvasive and selective tag for histidine and cysteine residues on the surface of cytochrome c at pH 5. The protein derivatives obtained are separable, and the tags are easily quantitated and differentiated through the metal-to-ligand charge transfer bands which are sensitive to the environment of the tag. Increasing the pH to 7.0 led to the modification by Pt(trpy)Cl{sup +}of Arg 91 in cytochrome c. Further studies with guanidine-containing ligands as models for arginine modification by Pt(trpy)Cl{sup +} showed that guanidine can act as a terminal ligand and as a bridging ligand. Owing to the potential utility of Pt(trpy)L{sup n+} as …
Date: September 21, 1990
Creator: Ratilla, Eva
System: The UNT Digital Library