Using Water and Gold Catalysts to Generate Novel Solutions for Current Energy Challenges: Purification of Hydrogen and Selective Oxidation of Methane

dc.contributor.advisorGrabow, Lars C.
dc.contributor.committeeMemberHarold, Michael P.
dc.contributor.committeeMemberPalmer, Jeremy C.
dc.contributor.committeeMemberWu, Judy I-Chia
dc.contributor.committeeMemberChandler, Bert
dc.creatorKanchari Bavajigari, Sravan Kumar
dc.creator.orcid0000-0003-3370-6336 2019 2019
dc.description.abstractRenewable hydrogen (H2) is touted to be a possible replacement for carbon based fuels in an effort to reduce greenhouse gas emissions. The current H2 production route through steam reforming of natural gas followed by water-gas shift treatment, however, indirectly releases CO2 and accounts for 3-5% of our global energy use. Moreover, the CO content in the effluent H2 stream from the water-gas shift reactor must be lowered for H2 applications that are sensitive to CO poisoning, for instance, fuel cells. In this work, supported gold catalysts in conjunction with water were used to purify hydrogen through preferential oxidation (PrOx) of CO with O2 in hydrogen-rich streams. The PrOx approach is a more energy efficient solution than the currently used CO methanation process. While water promotes O2 activation, it was found to poison the active metal-support interface (MSI) sites and kinetically hinder H2 activation at the MSI. Thus, water plays two distinct roles in enhancing the selectivity for CO oxidation during PrOx. In the current work, the role of water in inhibiting the undesired H2 oxidation reaction is probed with density functional theory, Fourier transform infrared (FTIR) spectroscopy and kinetic experiments. Methane is the primary component of shale gas and has attracted renewed attention to its potential direct conversion into value-added products such as methanol. The currently used two-stage process of steam reforming to synthesis gas, followed by methanol production from synthesis gas is only profitable at very large scale considering the high energy and infrastructure requirements. In contrast, single step conversion of methane to methanol is attractive for distributed processing and yields a liquid product directly. Environmentally benign O2 and water mixtures were found to generate active oxygen species at the Au/TiO2 MSI, avoiding the need to use expensive oxidants such as H2O2. In the current work, the possible pathways for methane upgrade are explored on Au/TiO2 using the activated oxygen species generated from O2/H2O mixtures.
dc.description.departmentChemical and Biomolecular Engineering, Department of
dc.format.digitalOriginborn digital
dc.identifier.citationPortions of this document appear in: Whittaker, Todd, KB Sravan Kumar, Christine Peterson, Meagan N. Pollock, Lars C. Grabow, and Bert D. Chandler. "H2 Oxidation over Supported Au Nanoparticle Catalysts: Evidence for Heterolytic H2 Activation at the Metal–Support Interface." Journal of the American Chemical Society 140, no. 48 (2018): 16469-16487. And in: Bruno, James E., K. B. Sravan Kumar, Nicolas S. Dwarica, Alexander Hüther, Zhifeng Chen, Clemente S. Guzman IV, Emily R. Hand et al. "On the Limited Role of Electronic Support Effects in Selective Alkyne Hydrogenation: A Kinetic Study of Au/MOx Catalysts Prepared from Oleylamine‐Capped Colloidal Nanoparticles." ChemCatChem 11, no. 6 (2019): 1650-1664.
dc.rightsThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
dc.subjectDensity functional theory
dc.subjectInfrared spectroscopy
dc.subjectSelective oxidation
dc.titleUsing Water and Gold Catalysts to Generate Novel Solutions for Current Energy Challenges: Purification of Hydrogen and Selective Oxidation of Methane
local.embargo.terms2021-12-01 College of Engineering and Biomolecular Engineering, Department of Engineering of Houston of Philosophy


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