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Articles 1 - 5 of 5
Full-Text Articles in Physical Sciences and Mathematics
H2 Oxidation Over Supported Au Nanoparticle Catalysts: Evidence For Heterolytic H2 Activation At The Metal-Support Interface, Todd N. Whittaker, K. B. Sravan Kumar, Christine Peterson, Meagan N. Pollock, L. C. Grabow, Bert D. Chandler
H2 Oxidation Over Supported Au Nanoparticle Catalysts: Evidence For Heterolytic H2 Activation At The Metal-Support Interface, Todd N. Whittaker, K. B. Sravan Kumar, Christine Peterson, Meagan N. Pollock, L. C. Grabow, Bert D. Chandler
Chemistry Faculty Research
Water adsorbed at the metal-support interface (MSI) plays an important role in multiple reactions. Due to its importance in CO preferential oxidation (PrOx), we examined H2 oxidation kinetics in the presence of water over Au/TiO2 and Au/Al2O3 catalysts, reaching the following mechanistic conclusions: (i) O2 activation follows a similar mechanism to that proposed in CO oxidation catalysis; (ii) weakly adsorbed H2O is a strong reaction inhibitor; (iii) fast H2 activation occurs at the MSI, and (iv) H2 activation kinetics are inconsistent with traditional dissociative H2 chemisorption on metals. Density …
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
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 …
Enhanced Oxygen Activation Over Supported Bimetallic Au-Ni Catalysts, Bert D. Chandler, Cormac G. Long, John D. Gilbertson, Christopher J. Pursell, G. Vijayaraghavan, K. J. Stevenson
Enhanced Oxygen Activation Over Supported Bimetallic Au-Ni Catalysts, Bert D. Chandler, Cormac G. Long, John D. Gilbertson, Christopher J. Pursell, G. Vijayaraghavan, K. J. Stevenson
Chemistry Faculty Research
New bimetallic Ni-Au supported nanoparticle catalysts were prepared by using dendrimer templated nanoparticles. Amine-terminated generation 5 polyamidoamine (PAMAM) dendrimers were anchored to a commercial silica with a siloxane linked anhydride. The dendrimer was then alkylated and used to template Ni-Au nanoparticles, which were subsequently extracted into organic solution as thiol monolayer protected clusters (MPCs). Transmission electron microscopy (TEM) and energy dispersive spectroscopy (EDS) indicated bimetallic nanoparticles of about 2 nm in size. Nanoparticles were deposited onto P-25 TiO2, and the capping thiol ligands were removed under flowing H2. DRIFTS infrared spectra of adsorbed CO showed only Au on the catalyst …
Patterning High Surface Area Silica With Lysozyme: Adsorption Kinetics, Fluorescence Quenching, And Protein Readsorption Studies To Evaluate The Templated Surface, Rachel M. Greer, Brittni A. Scruggs, R Alan May, Bert D. Chandler
Patterning High Surface Area Silica With Lysozyme: Adsorption Kinetics, Fluorescence Quenching, And Protein Readsorption Studies To Evaluate The Templated Surface, Rachel M. Greer, Brittni A. Scruggs, R Alan May, Bert D. Chandler
Chemistry Faculty Research
A method was developed for using an inexpensive and widely available protein, hen egg white lysozyme, as a patterning agent for commercial high surface area silicas. The basic patterning methodology involved spontaneous adsorption of the protein from aqueous solution, alkylation of the uncovered surface with an alkylsiloxane, and protein desorption in a slightly alkaline solution of morpholine. Adsorption kinetic studies using Bradford assays assisted in determining protein deposition conditions. These studies were generally consistent with results on more planar silica surfaces and indicated that the protein quickly and strongly adsorbs along its long axis at low surface coverages. A modified …
Origin Of Enantioselection In Chiral Alcohol Oxidation Catalyzed By Pd[(–)-Sparteine]Cl2, J. A. Mueller, Anne Cowell, Bert D. Chandler, M. S. Sigman
Origin Of Enantioselection In Chiral Alcohol Oxidation Catalyzed By Pd[(–)-Sparteine]Cl2, J. A. Mueller, Anne Cowell, Bert D. Chandler, M. S. Sigman
Chemistry Faculty Research
A kinetic investigation into the origin of enantioselectivity for the Pd[(–)-sparteine]Cl2-catalyzed aerobic oxidative kinetic resolution (OKR) is reported. A mechanism to account for a newly discovered chloride dissociation from Pd[(–)-sparteine]Cl2 prior to alcohol binding is proposed. The mechanism includes (1) chloride dissociation from Pd[(–)-sparteine]Cl2 to form cationic Pd(–)-sparteine]Cl, (2) alcohol binding, (3) deprotonation of Pd-bound alcohol to form a Pd-alkoxide, and (4) β-hydride elimination of Pd–alkoxide to form ketone product and a Pd–hydride. Utilizing the addition of (–)-sparteine HCl to control the [Cl–] and [H+] and the resulting derived rate law, …