Physical Sciences and Mathematics Commons^™

The Critical Role Of Water At The Gold-Titania Interface In Catalytic Co Oxidation, Johnny Saavedra, H. Doan, Christopher J. Pursell, L. C. Grabow, Bert D. Chandler

Chemistry Faculty Research

We provide direct evidence of a water-mediated reaction mechanism for room-temperature CO oxidation over Au/TiO2 catalysts. A hydrogen/deuterium kinetic isotope effect of nearly 2 implicates O-H(D) bond breaking in the rate-determining step. Kinetics and in situ infrared spectroscopy experiments showed that the coverage of weakly adsorbed water on TiO2 largely determines catalyst activity by changing the number of active sites. Density functional theory calculations indicated that proton transfer at the metal-support interface facilitates O2 binding and activation; the resulting Au-OOH species readily reacts with adsorbed Au-CO, yielding Au-COOH. Au-COOH decomposition involves proton transfer to water and was suggested to be …

Electrochemical Fabrication Of Two-Dimensional Flower-Like Pt Nanostructures For Methanol Electrocatalytic Oxidation, Xia Wang, Jun Hu, Yong-Jun Li

Journal of Electrochemistry

Two-dimensional flower-like Pt nanostructures (2D FPNs) were fabricated on glassy carbon substrates by galvanostatical electrochemical technique. The electrolyte was the HAuCl₄ + HClO₄ aqueous solution without addition of any structure-directing organic reagent, which made as-prepared Pt nanostructures cleaner, exhibiting much higher reactivity. Scanning electron microscopic images revealed that 2D FPNs were spherical Pt nano-flowers constructed by the smallest building blocks, nano-leaves. The number density of spherical Pt nano-flowers can be tuned by controlling the electrodeposition time. High resolution transmission electron microscopic images indicated that each nano-leaf was formed by growing along Pt(111) direction. Electrocatalytic activities of as-prepared 2D …

Characterization Of Organic Carbon In Sediments From Old Rifle, Co, A Former Uranium Mill, Francis Michael Tee, Morris Jones, Sharon Bone, Michael Schaefer, Scott Fendorf, John Bargar

STAR Program Research Presentations

Characterization of sediments from Old Rifle, CO, a former uranium mill

More than 34 million gallons (~129 million liters) of groundwater are contaminated with uranium at Old Rifle, Colorado – a former uranium-processing site that operated until 1958. The original Department of Energy strategy for remediation, involving natural flushing of U from the groundwater through mixing with surface water, has not been as successful as predicted. The uranium plume is replenished when insoluble U(IV) is oxidized to the more mobile U(VI). Relatively thin pockets of silt-, clay-, and organic-rich sediments contain reduced uranium, iron and sulfur and are referred to …

Selective Oxidations By Iron(Iii) Porphyrins And Iron(Iii) Corroles, Aaron Dalnamath Carver

Masters Theses & Specialist Projects

The selective oxidation of organic compounds represents a leading technology for chemical industries. They are used in chemical synthesis in the pharmaceutical and petrochemicals industries, and possible the decontamination of harmful substances. However, oxidations reaction are among the most challenging processes to control. Many stoichiometric oxidants with heavy metals are expensive, or toxic maybe both, and therefore unfeasible to be utilized. The ideal processes for catalytic oxidation would use molecular oxygen or hydrogen peroxide as the primary oxygen source, with transition metal catalysts to mimic the predominant oxidation catalysts in Nature, the cytochrome P450 enzymes. This study focuses on the …

Speciation Behavior Of Americium Higher Oxidation States For The Separation Of Americium From Curium, Catherine Lynn Riddle

UNLV Theses, Dissertations, Professional Papers, and Capstones

Several countries are currently expanding the use of nuclear energy as a method for the safe generation of carbon free energy and a number are evaluating starting up a nuclear power program. Closed fuel cycle technologies may be key to waste reduction and a sustainable nuclear energy future and to support the development of more efficient fuel cycles, the investigation of the chemical properties of key actinides is at the forefront of separations research. In this work the characterization of higher oxidation states of americium (Am) has been performed using spectroscopic methods. Americium in the formal oxidation state of Am(V) …

Selective Oxidations By Metalloporphyrins And Metallocorroles, Tse-Hong Chen

Masters Theses & Specialist Projects

Highly reactive transition metal-oxo intermediates are important active oxidant involved in numerous enzymes such as cytochrome P450 monooxygenases as well as in many useful metal-catalyzed oxidations. Many transition metal catalysts are designed for biomimetic studies of the predominant oxidation catalysts in Nature, the cytochrome P450 enzymes. In this work, a series of metalloporphyrin and metallocorrole complexes have been successfully synthesized and spectroscopically characterized by UV-vis, GCMS and ¹H-NMR. The utilization of these complexes as catalysts for selective oxidation of sulfides and photocatalytic aerobic oxidations of activated hydrocarbons were investigated. Ruthenium(II) porphyrin complexes (2) and iron(III) corrole complexes (4) with …

Big Horned, Juniper Harrower

The STEAM Journal

Tinta y tinto (Spanish for black ink and red wine)
Through a process of oxidation, reduction, and light manipulation, Juniper stains and colors paper with red wine and a rich black pigment made of the wild harvested mushroom Coprinopsis atramentaria.

Pulse Electrodeposition Of Pd-Ni Alloy Nanoparticles For Electrocatalytic Oxidation Of Formic Acid, Fang-Zu Yang, Jun-Pei Yue, Zhong-Qun Tian, Shao-Min Zhou

Journal of Electrochemistry

The Pd-Ni alloy nanoparticles with nickel atomic contents of 12.0%, 16.4% and 22.6% were successfully electrodeposited from a Pd-Ni alloy electrolyte by square wave pulse plating. The alloy nanoparticles were in the spherical shape with a diameter of 50 ~ 80 nm. As the growth potential of the alloy was negatively shifted, the nickel content of the alloy was increased, and the size of the nanoparticles was almost the same, whereas the number, the degree of crosslinking and the real active area of the nanoparticles were increased. As the nickel content of the alloy nanoparticles increased, the peak current for …

Anodic Strategies For The Covalent Attachment Of Molecules To Electrodes Through Ethynyl And Vinyl Linkages, Matthew Vincent Sheridan

Graduate College Dissertations and Theses

Substrates with localized, organic radicals have the ability to attack `inert' surfaces to form covalent bonds between the substrate and an atom at the surface. These radicals can be generated in electrochemical experiments with substrates bearing an electroactive moiety. The moiety after oxidation (loss of an electron) or reduction (gain of an electron) generates the active radical. Electron transfer reactions at an electrode surface generate a high population of these radicals, thereby facilitating attachment.

The electrochemical oxidations of compounds containing terminal alkynes and alkenes were found to be effective methods for covalent attachment to glassy carbon, gold, and platinum electrodes. …

Electronic Effects In Oxidation Reactions Utilizing Dinuclear Copper Complexes With The Bis[3-(2-Hydroxybenzylideneamino)Phenyl] Sulfone Ligand, Armando M. Guidote Jr, Ronald L. Reyes, Riyo Kashihara, Yasuhiko Kurusu, Yoshihiro Masuyama

Chemistry Faculty Publications

Copper acetate and the ligands bis[3-(3-tert-butyl-2-hydroxy-5-methoxybenzylideneamino)phenyl] sulfone and bis[3-(3,5-di-tert-butyl-2-hydroxybenzylideneamino)phenyl] sulfone were reacted to form the complexes with 2:1 copper:ligand ratio, Cu2[B(t-Bu) (OMe)BAPS](µ-OCH3)2 (4) and with 2:2 copper:ligand ratio, Cu2[B(t-Bu)2BAPS]2 (5), respectively. Structures of 4 and 5 were determined based on IR, UV-Vis, and FAB-MS data in comparison with previously characterized related copper complexes. The two complexes 4 and 5 were utilized in the oxidation of the substrates 2,4- and 2,6-di-tertbutylphenol (dtbp) at -50C with H2O2 in CH2Cl2. The coupling products are preferred in both cases. For 2,4-dtbp, yields of 4,600% and 7,200% of 3,3’,5,5’-tetra-tert-butyl-2,2’- biphenol were achieved with the use …

Oxidation Of Hydrocarbons With Tetra-N-Butylammonium Peroxy Monosulfate Catalyzed By \Beta-Tetrabromo-Meso-Tetrakis(4-Methoxyphenyl)- And \Beta-Tetrabromo-Meso-Tetraphenylporphyrinatomanganese(Iii), Saeed Rayati, Saeed Zakavi, Hossein Valinejad

Turkish Journal of Chemistry

\beta-Tetrabromo-meso-tetrakis(4-methoxyphenyl)porphyrin, H_2T(4-OCH_3P)PBr_4, was synthesized and characterized by UV-Vis and ^1H NMR spectroscopy. Oxidation of alkanes and olefins with tetra-n-butylammonium peroxymonosulfate (n-Bu_4NHSO_5) was studied in the presence of MnT(4-OCH_3P)PBr_4(OAc) and MnTPPPBr_4(OAc) (TPP = meso-tetraphenylporphyrin). While significance differences were observed between the catalytic activities of the title complexes in the oxidation of alkanes, the 2 manganese porphyrins showed comparable activities in oxidation of most of the olefins used. However, the latter showed greater catalytic performance in the oxidation of the hydrocarbons. Moreover, the oxidative degradation of the former (60 %) was greater than that of the latter (45 %) in the oxidation …

N-Bridged Dimers Of Tetrapyrroles Complexed By Transition Metals: Syntheses, Characterization Methods, And Uses As Oxidation Catalysts, Ümi̇t İşci̇, Fabienne Dumoulin, Alexander B. Soroki̇n, Vefa Ahsen

Turkish Journal of Chemistry

N-bridged dimers of tetrapyrroles complexed by transition metals have been known for nearly four decades, and gained renewed attention when their powerful oxidation properties were recently evidenced. This article is a state of the art review of the reported complexes and of their synthetic methods. Beyond classical chemistry characterization tools, specific methods appropriate to their structure are used and are presented in detail. Finally, their uses and importance of oxidation catalysts are reviewed.

Selective Oxidation Of Sulfides And Hydrocarbons With H_2o_2 Over Manganese Catalyst Supported On Nanoparticles, Massomeh Ghorbanloo, Roghayeh Tarasi, Jun Tao, Hidenori Yahiro

Turkish Journal of Chemistry

A new magnetically separable catalyst consisting of binuclear Mn(II) complex [Mn_2(HL)_2(H_2O)_4], HL = 2-[(2-hydroxy-benzylidene)-amino]-3-(4-hydroxyphenyl)-propionic acid, supported on (3-chloropropyl)-trimethoxysilane (CPTMS) functionalized silica-coated magnetic nanoparticles (MNPs) was prepared. The synthesized catalyst was characterized by several physico-chemical and spectroscopic methods. This immobilized complex was found to be an efficient heterogeneous catalyst for the oxidation of different sulfides and hydrocarbons using hydrogen peroxide (H_2O_2) as an oxidant. The catalyst is readily recovered by simple magnetic decantation and can be recycled several times with no considerable loss of catalytic activity.