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Articles 31321 - 31350 of 33287
Full-Text Articles in Entire DC Network
Effects Of N2h4 On The Transition Temperature In The Anisotropic Superconductor Tase3, K. Yamaya, T. H. Geballe, Juana Vivó Acrivos, J. Code
Effects Of N2h4 On The Transition Temperature In The Anisotropic Superconductor Tase3, K. Yamaya, T. H. Geballe, Juana Vivó Acrivos, J. Code
Faculty Publications, Chemistry
No abstract provided.
Mott G-Ratios In Rbx(Nh3)1-X And Oxidation State Of Rubidium Compounds From Xas, Juana Vivó Acrivos, K. Hathaway, A. Robertson, M. P. Klein, A. Thompson
Mott G-Ratios In Rbx(Nh3)1-X And Oxidation State Of Rubidium Compounds From Xas, Juana Vivó Acrivos, K. Hathaway, A. Robertson, M. P. Klein, A. Thompson
Faculty Publications, Chemistry
The x-ray absorption spectra (XAS) of Rb metal, Rh,("JH,J, ,, 2H-NbSe2Rb111x and RbBr near the Rb K-edge have been used to ascertain that the oxidation state V of rubidium dissolved in ammonia and intt:rcalated in the layer compound is in the range 0 < V < I. Theobservededge shifts with temperature for semimctals are explainedin terms of the population of band states, and the ratio of the density states near the mobility edge over that calculated for a free electron model, i.e. the Mott ratio g, is ascertained using a semiempirical relation developed for the x-ray absorbance from Is levels to empty states ncar the mobility edge.
A Rolling Laboratory Platform For The Mobility Handicapped, John T. Moore
A Rolling Laboratory Platform For The Mobility Handicapped, John T. Moore
Faculty Publications
Portable laboratory stations designed for use by the mobility handicapped are available, but the expense of these precludes their use by many institutions. These authors share a more affordable solution.
Proton Transfers In Hydrogen‐Bonded Systems. Vi. Electronic Redistributions In (N2h7)+ And (O2h5)+, Steve Scheiner
Proton Transfers In Hydrogen‐Bonded Systems. Vi. Electronic Redistributions In (N2h7)+ And (O2h5)+, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
Electronic rearrangements accompanying transfer of the central proton between the two XHn units of (H3NHNH3)+ and (H2OHOH2)+ are studied using ab initio molecular orbital methods. Electron density difference maps are calculated by subtracting the density of the equilibrium structure (X–H‐‐‐X) from that of the midpoint geometry (X‐‐H‐‐X) using the split‐valence 4‐31G basis set. Some of the features revealed by the maps are common to both systems while others indicate significant differences between nitrogen and oxygen. Decomposition of the total electron density into …
A White Ammonia Fountain, John T. Moore
A White Ammonia Fountain, John T. Moore
Faculty Publications
Red, white, and blue ammonia fountains are a stunning addition to chemistry magic shows.
Effect Of Solvent On Properties Of The Liquid Metal Surface, J. P. Badiali, M. I. Rosinberg, Jerry Goodisman
Effect Of Solvent On Properties Of The Liquid Metal Surface, J. P. Badiali, M. I. Rosinberg, Jerry Goodisman
Chemistry - All Scholarship
We calculate the difference in the surface potentials between the free surface of a liquid metal and the same metal in an ideally polarizable interface at the point of zero charge. This difference, δXm, is due to the deformation of the electronic cloud of the metal by the solvent molecules. The simple model used for the free (metal-metal vapor) surface yields qualitatively correct work functions for a number of metals (Hg, Cd, In, Zn, Pb, Ga, A1). Two simple ways to model the metal-solvent interaction are proposed and calculations of δXm made for each. One, the dielectric film model, considers …
Pyridine Hydrogen Iodide As An Ether Cleaving Agent In Coal Chemistry, Agnes Mei-Ying Chen
Pyridine Hydrogen Iodide As An Ether Cleaving Agent In Coal Chemistry, Agnes Mei-Ying Chen
Masters Theses
Reactions of several phenyl ethers and an ester with pyridine hydrogen iodide were examined under various conditions as model studies for the recently reported molecular weight reduction of a fraction of Illinois No. 6 coal by hydrogen iodide in pyridine at 50°.
No ether or ester cleavage was observed at 60-80° in pyridine, acetonitrile, ethanol or the absence of solvent. Sealed tube reactions at 210° resulted in cleavage to phenol plus various hydrocarbon and alkyl halide products. Pyridine and benzyl phenyl ether at 210° produced no cleavage in the absence of hydrogen iodide.
Syntheses of crystalline pyridine hydrogen iodide and …
A Matrix Isolation Study Of The Reactions Of Oxygen(Singlet-D) With The Chlorofluoromethanes Fluorotrichloromethane, Dichlorodifluoromethane And Chlorotrifluoromethane, Richard Thomason Burke
A Matrix Isolation Study Of The Reactions Of Oxygen(Singlet-D) With The Chlorofluoromethanes Fluorotrichloromethane, Dichlorodifluoromethane And Chlorotrifluoromethane, Richard Thomason Burke
University of the Pacific Theses and Dissertations
We have studied the reactions of O(1D) with CC13F, CC12F2 and CC1F3 in CO2, SF6 and N2O matrices, and in neat mixtures. Photolysis of cryogenic mixtures of ozone and the chlorofluoromethanes in various matrix hosts resulted in production of O(1D) which migrated through the matrix to react with the Freon molecules. Products were detected by infrared spectroscopy of the matrix deposits, with assignments confirmed by comparison of 16O and 18O absorption bands with literature values. Evidence for oxygen atom insertion into a C-C1 …
Glow Discharge Polymerization., H. Yasuda
Glow Discharge Polymerization., H. Yasuda
Chemistry Faculty Research & Creative Works
In this review-paper the author summarizes some important aspects of ″polymer formation″ in the glow discharge polymerization or plasma polymerization, rather than presenting a bibliographical review of work. It is shown that glow discharge polymerization can be visualized as a process consisting of three discharge processes. These are (1) controlled discharge of monomer, (2) electric discharge (glow discharge), and (3) glow discharge polymerization of the monomer. Before the electric discharge is initiated, a steady-state flow of the monomer is generally established. During this controlled discharge of the monomer (without electric discharge), adsorption of the monomer onto the solid surfaces in …
Conduction Band Symmetry In Ta Chalcogenides From Ta L Edge X-Ray Absorption Spectroscopy (Xas), Juana Vivó Acrivos, S.S. P. Parkin, J. Code, J. Reynolds, K. Hathaway, H. Kurasaki, E. Marseglia
Conduction Band Symmetry In Ta Chalcogenides From Ta L Edge X-Ray Absorption Spectroscopy (Xas), Juana Vivó Acrivos, S.S. P. Parkin, J. Code, J. Reynolds, K. Hathaway, H. Kurasaki, E. Marseglia
Faculty Publications, Chemistry
No abstract provided.
Spectroscopic Studies Of Pre-Mixed Hydrocarbon Flame Plasmas, Tsao-Chin C. Huang
Spectroscopic Studies Of Pre-Mixed Hydrocarbon Flame Plasmas, Tsao-Chin C. Huang
Masters Theses
This thesis contains two different studies.
Chapter 1, "Infrared Emission Spectrum of the Hydroxyl Radical.", is in collaboration with Dr. Giles L. Henderson and Mr. Chun-Sheng Ko. This chapter has been submitted and accepted for publication by the Journal of Chemical Education.
In this chapter, we describe a rather novel physical chemistry experiment in which ab initio potential parameters for the OH radical are compared with those obtained from the ir emission spectrum of an oxy-acetylene welding torch.
Chapter 2, "A Preliminary Spectroscopic Study of Field-Induced Ion Movements in Flame Gases.", describes the effects of longitudinal electric fields on CH …
Controlling The Number Of Metal Sites To Which A Polytertiary Phosphine Coordinates In Tungsten Carbonyls, Rodney D. Borger
Controlling The Number Of Metal Sites To Which A Polytertiary Phosphine Coordinates In Tungsten Carbonyls, Rodney D. Borger
Masters Theses
Judiciously selected coordinated fragments of Ph2PCH2CH2PPhCH2-CH2PPh2 [(OC)5WPPh2H, (OC)5WPPh2CH=CH2 and (OC)5WPPh(CH=CH2)2] were used to construct its five possible nonchelated pentacarbonyltungsten complexes. These are the trimetallic (OC)5WPPh[CH2CH2PPh2W(CO)5]2 and the two pairs of constitutional isomers, (OC)5WPPh[CH2CH2PPh2]2 and (OC)5WPPh2CH2CH2PPhCH2CH2PPh2, and PPh[CH2CH2 …
Analysis Of Coal Fractions Using Dibromotriphenyl-Phosphorane: A Selective Ether Cleaving Reagent, Michael L. Ballard
Analysis Of Coal Fractions Using Dibromotriphenyl-Phosphorane: A Selective Ether Cleaving Reagent, Michael L. Ballard
Masters Theses
Dibromotriphenylphosphorane (DTP), in acetonitrile at 40°C, was found to cleave benzyl phenyl ether in preference to di-alkyl or other aryl alkyl ethers. Competition between 10 mmoles benzyl phenyl ether and 10 mmoles di-n-octyl ether for 0.92 mmole of DTP gave 48% cleavage of benzyl phenyl ether and 1.3% cleavage of di-n-octyl ether based on DTP. Reaction of benzyl phenyl ether and di-n-octyl ether separately with DTP at 40°C produced 80% and 8% cleavage, respectively. Reactions of DTP with diphenyl ether, butyl phenyl ether, phenyl cyclohexyl ether and benzyl benzoate at 40°C produced less than 3% cleavage in all cases.
Reaction …
Cis Labilization: A Study Of The Reactions Of Group 6 Pentacarbonyl Phosphido Anions, Matthew J. Madigan
Cis Labilization: A Study Of The Reactions Of Group 6 Pentacarbonyl Phosphido Anions, Matthew J. Madigan
Masters Theses
The synthesis of cis-(OC)4M(PPh2H)L (M=Cr,Mo,W; L=PPh3,PPh2Et,PPhEt2,PEt3) can be achieved by treating (OC)5MPPh2H with potassium tert-butoxide in the presence of L. […] The products are easily isolated and are not contaminated with trans isomers. Obtained as a minor product is [(OC)4MPPh2]2.
The reaction of (OC)5WPPh2H with potassium tert-butoxide generates [(OC)5WPPh2]- which reacts with (OC)5WPPh2H to give [(OC)5WPPh2W(CO)5] …
Mode Of Action Of The Heme-Controlled Translational Inhibitor: Relationship Of Eukaryotic Initiation Factor 2-Stimulating Protein To Translation Restoring Factor., John Siekierka, Ken-Ichiro Mitsui, Severo Ochoa
Mode Of Action Of The Heme-Controlled Translational Inhibitor: Relationship Of Eukaryotic Initiation Factor 2-Stimulating Protein To Translation Restoring Factor., John Siekierka, Ken-Ichiro Mitsui, Severo Ochoa
Department of Chemistry and Biochemistry Faculty Scholarship and Creative Works
We have purified the translation restoring factor (RF) and the eukaryotic initiation factor 2 (eIF-2) stimulating protein (ESP) to near homogeneity from the postribosomal supernatant and the ribosomal salt wash, respectively, of rabbit reticulocyte lysate. They were isolated in the form of eIF-2 complexes, apparently in a 1:1 ratio. Their virtually identical NaDodSO4/polyacrylamide gel electrophoretic patterns show, in addition to the eIF-2 alpha (38,000), beta (52,000), and gamma (54,000) bands, peptide bands at approximately 80, 65, 57, 40, and 32 kilodaltons. The apparent Mr of either complex is about 450,000, whereas that of free translation restoring factor (RF) is approximately …
Similarity In Phase Diagrams Between Ionic And Nonionic Surfactant Solutions At Constant Temperature, K. Shinoda, H. Kunieda, N. Obi, Stig Friberg
Similarity In Phase Diagrams Between Ionic And Nonionic Surfactant Solutions At Constant Temperature, K. Shinoda, H. Kunieda, N. Obi, Stig Friberg
Chemistry Faculty Research & Creative Works
No abstract provided.
Neutron Activation Analysis Of Nuclides From Stellar And Man-Induced Nuclear Reactions, Lawrence Lee Oliver
Neutron Activation Analysis Of Nuclides From Stellar And Man-Induced Nuclear Reactions, Lawrence Lee Oliver
Doctoral Dissertations
"Neutron activation and γ-counting were used to determine the relative abundances of six stable tellurium isotopes in the acid-etched residues of the Allende meteorite. The results were correlated with the isotopic compositions of xenon and the elemental abundances of helium and neon in similarly prepared residues. Nucleosynthesis appears to be the only viable explanation for the anomalous isotopic and elemental compositions observed in these residues. Our results suggest that the solar system condensed from an isotopically and chemically zoned nebula that was produced by the explosion of a supernova, concentric with the present sun.
A combination of neutron activation and …
Distribution Of Polymer Deposition In Glow Discharge Polymerization In A Capacitively Coupled System, N. Inagaki, H. Yasuda
Distribution Of Polymer Deposition In Glow Discharge Polymerization In A Capacitively Coupled System, N. Inagaki, H. Yasuda
Chemistry Faculty Research & Creative Works
The manner by which polymers created by plasma uniformly deposit onto substrates was sought. By rotating the substrate placed midway between electrodes, completely uniform distribution of polymer deposition was accomplished, and the deviation of the polymer deposition in a radius direction of the rotating substrate was within experimental errors. Materials of the substrate on which the polymer deposited had no influence on uniformity of polymer deposition, but the electrical circuit of power source, i.e., grounding an electrode, markedly disturbed the uniformity. Thickness of polymers deposited on the substrate was linearly proportional to reaction time. Surface energies of deposited polymers prepared …
Sodium Accumulation In Serpentine And Non-Serpentine Populations Of The Milkweed Asclepias Fascicularis, Paul N. Thomas
Sodium Accumulation In Serpentine And Non-Serpentine Populations Of The Milkweed Asclepias Fascicularis, Paul N. Thomas
University of the Pacific Theses and Dissertations
Because Asclepias fascicularis is found on both serpentine and non-serpentine soils in California and because it was reported to accumulate sodium, this study was initiated to establish the degree of accumulation of this ion in these two soil types. Two other species, Asclepias speciosa Torr. and Asclepias cordifolia (Benth.) Jeps. were included to determine if this characteristic of accumulation occurs in other members of this genus.
The Initial And Terminating Stage Of Glow Discharge Polymerization Investigated By Thickness Monitor, N. Inagaki, H. Yasuda
The Initial And Terminating Stage Of Glow Discharge Polymerization Investigated By Thickness Monitor, N. Inagaki, H. Yasuda
Chemistry Faculty Research & Creative Works
An attempt to discuss the initial stage and terminating stage of glow discharge polymerization was made by selecting the monomer system of styrene and acetylene, which differ in their condensability, and a certain polymerization procedure. Results indicate the important aspects of the initial and terminating stages of glow discharge polymerization. These aspects may not play a significant role in the study of bulk properties of plasma‐polymerized polymers or in the study of polymer deposition rate. However, the initial stage effect might influence the adhesion of the polymer. The terminating stage effect might influence the surface characteristics of glow discharge‐polymerized polymers. …
Adhesion Of Glow Discharge Polymers To Metals And Polymers, N. Inagaki, H. Yasuda
Adhesion Of Glow Discharge Polymers To Metals And Polymers, N. Inagaki, H. Yasuda
Chemistry Faculty Research & Creative Works
Adhesion of glow discharge polymers to metals and polymers in an adhesive joint was measured by lap‐shear test and immersion in hot water of 70°C for an extended time. A glow discharge polymer was deposited onto polymers [polyethylene and poly(tetrafluoroethylene)] and metals (aluminum and stainless steel) prior to when the polymer and metal were joined. It is found that the lap‐shear strength is enhanced by coating the surfaces of these substrates with plasma film produced from methane, ethylene, and acetylene, and that deterioration of the adhesive bonding part, when immersed in hot water of 70°C, is strongly dependent on the …
The Effect Of Plasma-Deposited Polymers On The Nucleate Boiling Behavior Of Copper Heat Transfer Surfaces, T. Hinrichs, E. Hennecke, H. Yasuda
The Effect Of Plasma-Deposited Polymers On The Nucleate Boiling Behavior Of Copper Heat Transfer Surfaces, T. Hinrichs, E. Hennecke, H. Yasuda
Chemistry Faculty Research & Creative Works
The effect of plasma deposited polymers on the nucleate boiling behavior of copper heat transfer surfaces, using water as the boiling liquid, was determined. The monomers used were tetrafluoroethylene (TFE) and methane. It was found that an 18 nm thick coating of TFE enhanced the nucleate boiling, while a 150 nm thick coating reduced the nucleate boiling. Both 15 nm and 150 nm thick coatings of methane reduced the nucleate boiling, with the effect being more pronounced with the thicker coating. A surface energy effect is postulated to explain the enhanced boiling observed. © 1981.
The Structure Of Lamellar Lyotropic Liquid Crystals From Lecithin And Alkanediols, Magda A. El-Nokaly, Larry D. Ford, Stig Friberg, David W. Larsen
The Structure Of Lamellar Lyotropic Liquid Crystals From Lecithin And Alkanediols, Magda A. El-Nokaly, Larry D. Ford, Stig Friberg, David W. Larsen
Chemistry Faculty Research & Creative Works
Lamellar liquid crystals from lecithin and alkane diols were studied to determine the composition range of stability and geometrical dimensions using low-angle X-ray scattering. An estimation of the dislocation pattern was made from the optical pattern in polarized light. The ethylene glycol gave the widest range of stability for the lamellar structure, the range being reduced toward heptane diol, the longest member to give liquid crystals. The interlayer spacing was reduced with increasing chain length of the diol and the dislocation pattern remained identical. © 1981.
Method For Direct Preparation For 1,2,4-Triazole From Hydrazine And Formamide, Harris E. Petree, Joseph R. Pociask, John T. Gupton
Method For Direct Preparation For 1,2,4-Triazole From Hydrazine And Formamide, Harris E. Petree, Joseph R. Pociask, John T. Gupton
Chemistry Faculty Publications
Process for the preparation of 1,2,4-triazole comprises contacting hydrazine or its aqueous solutions with at least about 2.5 moles of formamide at a temperature of 140° to 210° C. and then recovering the resultant 1,2,4- triazole in yields of 92-98% with 94-98% purity. The formamide is maintained in an excess over about the 2.5 molar amount consumed in the reaction with the hydrazine. Recovery steps for isolating the 1,2,4-triazole are disclosed.
Thermal Decomposition Kinetics Of Asf5-Doped Polyacetylene In Vacuum, T. Inoue, J. E. Osterholm, H. Yasuda, L. L. Levenson
Thermal Decomposition Kinetics Of Asf5-Doped Polyacetylene In Vacuum, T. Inoue, J. E. Osterholm, H. Yasuda, L. L. Levenson
Physics Faculty Research & Creative Works
Electrical conductivity measurements, mass spectra of desorbing species, and ESCA surface analysis are reported for AsF5-doped polyacetylene heated between 50 and 130°C in vacuum. All measurements indicate first-order decomposition kinetics with activation energies between 13 and 20 kcal mole-1. Decomposition leads to the desorption of AsF3 and F2. Metallic arsenic remains in the polyacetylene as a decomposition by-product.
Iron And Life, Thomas Emery
Iron And Life, Thomas Emery
Faculty Honor Lectures
Iron, iron, everywhere but. . . . The plight of the ancient mariner surrounded by undrinkable water could hardly have been more frustrating than life on earth with respect to iron. Iron is the fourth most abundant element of the earth's surface, exceeded only by oxygen, silicon, and aluminum. Virtually all forms of life from the simplest bacteria to humans require iron to catalyze numerous and complex metabolic reactions. Because of the diversity and complexity of the role of iron in the life process, it has even been suggested that the origin of life on earth centered around the catalytic …
22nd Rocky Mountain Conference On Analytical Chemistry
22nd Rocky Mountain Conference On Analytical Chemistry
Rocky Mountain Conference on Magnetic Resonance
Abstracts and meeting program from the 22nd annual meeting of the Rocky Mountain Conference on Analytical Chemistry, co-sponsored by the Rocky Mountain Section of the Society for Applied Spectroscopy and the Rocky Mountain Chromatography Discussion Group. Held in Denver, Colorado, August 10-14, 1980.
Stereochemistry And Circular Dichorism Of Some Cobalt(Iii) Complexes With Ethylenediamine-N, N’-Diacetic Acid And N, N'-Dimethylethylenediamine-N ,N'-Diacetic Acid, Godfrey Chinenye Mbah
Stereochemistry And Circular Dichorism Of Some Cobalt(Iii) Complexes With Ethylenediamine-N, N’-Diacetic Acid And N, N'-Dimethylethylenediamine-N ,N'-Diacetic Acid, Godfrey Chinenye Mbah
Dissertations
Two series of complexes trans-{Co(LL')EDDA}('+) and trans-{Co(LL')DMEDDA}('+), LL' = Meen, 2-Mepn, udmeen, sdmeen, R-dmepn were prepared. EDDA was reacted with cobalt(II) carbonate and the resulting solution combined with the diamine of choice. For the DMEDDA complexes the ligand DMEDDA was first prepared by adding neutralized chloroacetic acid to sdmeen and precipitating out the ligand as the barium salt. The DMEDDA complexes were prepared by reacting the barium salt first with cobalt(II) sulfate and then with the diamines listed above except udmeen. The DMEDDA complexes with R-pn were also prepared. For both series the oxidation of the Co(II) to Co(III) was …
Phase Transition Effects: A Crystallographic Characterization Of The Temperature Dependency Of The Crystal Structure Of The 1:1 Charge Transfer Complex Between Anthracene And Tetracyanobenzene In The Temperature Range 297 To 119 K, John J. Stezowski
John J. Stezowski Publications
Crystal structures of the charge transfer complex between anthracene and tetracyanobenzene, A:TCNB, C14H10: C10H2N4, at three temperatures (297, 234 and 226 K) above the order–disorder phase transition at 206 K and at four temperatures (202, 170, 138, and 119 K) below it have been determined from x-ray diffraction data. The space group of the room temperature phase was assigned as Cm with a = 9.528(2), b =12.779(3), c = 7.441(2) Å and β=92.39(2) degrees at 297 K and for the low temperature phase is P21/a with a =9.457(1), …
Evolution Of A Cooling Water Treatment Program At A Chemical Processing Plant, Lawrence P. Everson
Evolution Of A Cooling Water Treatment Program At A Chemical Processing Plant, Lawrence P. Everson
Retrospective Theses and Dissertations
During the construction of a chemical processing plant, a polyphosphate product was selected for use as a corrosion inhibitor in the open recirculating cooling tower system. After several months of operation, problems in the system made evident the fact that polyphosphate as a corrosion inhibitor was not acceptable. An organic corrosion inhibitor was substituted for the phosphate, resulting in improved corrosion protection and the elimination of phosphate fouling.