scholarly journals In situ UV−Visible Spectroscopic Measurements of Kinetic Parameters and Active Sites for Catalytic Oxidation of Alkanes on Vanadium Oxides†

2005 ◽  
Vol 109 (6) ◽  
pp. 2414-2420 ◽  
Author(s):  
Morris D. Argyle ◽  
Kaidong Chen ◽  
Enrique Iglesia ◽  
Alexis T. Bell
Keyword(s):  
Kinetic Parameters ◽  
Catalytic Oxidation ◽  
Active Sites ◽  
Vanadium Oxides ◽  
Spectroscopic Measurements ◽  
Uv Visible

scholarly journals Extent of Reduction of Vanadium Oxides during Catalytic Oxidation of Alkanes Measured by in-Situ UV−Visible Spectroscopy

2004 ◽  
Vol 108 (7) ◽  
pp. 2345-2353 ◽  
Author(s):  
Morris D. Argyle ◽  
Kaidong Chen ◽  
Carlo Resini ◽  
Catherine Krebs ◽  
Alexis T. Bell ◽  
...  
Keyword(s):  
Catalytic Oxidation ◽  
Vanadium Oxides ◽  
Visible Spectroscopy ◽  
Uv Visible

In situ mid-IR and UV–visible spectroscopies applied to the determination of kinetic parameters in the anionic copolymerization of styrene and isoprene

Polymer ◽  
2009 ◽  
Vol 50 (6) ◽  
pp. 1351-1357 ◽  
Author(s):  
Sébastien Quinebèche ◽  
Christophe Navarro ◽  
Yves Gnanou ◽  
Michel Fontanille
Keyword(s):  
Kinetic Parameters ◽  
Uv Visible ◽  
Anionic Copolymerization

scholarly journals Electrokinetic and in situ spectroscopic investigations of CO electrochemical reduction on copper

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jing Li ◽  
Xiaoxia Chang ◽  
Haochen Zhang ◽  
Arnav S. Malkani ◽  
Mu-jeng Cheng ◽  
...  
Keyword(s):  
Mass Transport ◽  
Active Sites ◽  
Gas Diffusion ◽  
Reduction Reaction ◽  
Adsorbed Hydrogen ◽  
Diffusion Type ◽  
Proton Coupled Electron Transfer ◽  
Alkaline Electrolytes ◽  
Reaction Orders

AbstractRigorous electrokinetic results are key to understanding the reaction mechanisms in the electrochemical CO reduction reaction (CORR), however, most reported results are compromised by the CO mass transport limitation. In this work, we determined mass transport-free CORR kinetics by employing a gas-diffusion type electrode and identified dependence of catalyst surface speciation on the electrolyte pH using in-situ surface enhanced vibrational spectroscopies. Based on the measured Tafel slopes and reaction orders, we demonstrate that the formation rates of C2+ products are most likely limited by the dimerization of CO adsorbate. CH4 production is limited by the CO hydrogenation step via a proton coupled electron transfer and a chemical hydrogenation step of CO by adsorbed hydrogen atom in weakly (7 < pH < 11) and strongly (pH > 11) alkaline electrolytes, respectively. Further, CH4 and C2+ products are likely formed on distinct types of active sites.

scholarly journals Identification of Active Sites in the Catalytic Oxidation of 2‐Propanol over Co1+xFe2‐xO4 Spinel Oxides at Solid/Liquid and Solid/Gas Interfaces

ChemCatChem ◽  
2021 ◽  
Author(s):  
Tobias Falk ◽  
Eko Budiyanto ◽  
Maik Dreyer ◽  
Christin Pflieger ◽  
Daniel Waffel ◽  
...  
Keyword(s):  
Catalytic Oxidation ◽  
Active Sites ◽  
Spinel Oxides ◽  
Solid Liquid

scholarly journals Microbial N2O consumption in and above marine N2O production hotspots

2020 ◽  
Author(s):  
Xin Sun ◽  
Amal Jayakumar ◽  
John C. Tracey ◽  
Elizabeth Wallace ◽  
Colette L. Kelly ◽  
...  
Keyword(s):  
Kinetic Parameters ◽  
Substrate Affinity ◽  
N2o Production ◽  
Anoxic Waters ◽  
Production And Consumption ◽  
Consumption Rates ◽  
Anoxic Zones ◽  
First Time ◽  
Microbial N

AbstractThe ocean is a net source of N2O, a potent greenhouse gas and ozone-depleting agent. However, the removal of N2O via microbial N2O consumption is poorly constrained and rate measurements have been restricted to anoxic waters. Here we expand N2O consumption measurements from anoxic zones to the sharp oxygen gradient above them, and experimentally determine kinetic parameters in both oxic and anoxic seawater for the first time. We find that the substrate affinity, O2 tolerance, and community composition of N2O-consuming microbes in oxic waters differ from those in the underlying anoxic layers. Kinetic parameters determined here are used to model in situ N2O production and consumption rates. Estimated in situ rates differ from measured rates, confirming the necessity to consider kinetics when predicting N2O cycling. Microbes from the oxic layer consume N2O under anoxic conditions at a much faster rate than microbes from anoxic zones. These experimental results are in keeping with model results which indicate that N2O consumption likely takes place above the oxygen deficient zone (ODZ). Thus, the dynamic layer with steep O2 and N2O gradients right above the ODZ is a previously ignored potential gatekeeper of N2O and should be accounted for in the marine N2O budget.

The AMPIX electrochemical cell: a versatile apparatus forin situX-ray scattering and spectroscopic measurements

2012 ◽  
Vol 45 (6) ◽  
pp. 1261-1269 ◽  
Author(s):  
Olaf J. Borkiewicz ◽  
Badri Shyam ◽  
Kamila M. Wiaderek ◽  
Charles Kurtz ◽  
Peter J. Chupas ◽  
...  
Keyword(s):  
Electrochemical Cell ◽  
Function Analysis ◽  
Kinetic Studies ◽  
Spectroscopic Measurements ◽  
Battery Materials ◽  
X Ray ◽  
Complex Processes ◽  
Electrochemical Cycling ◽  
Ray Scattering

This article presents a versatile easy-to-use electrochemical cell suitable forin operando,in situmeasurements of battery materials during electrochemical cycling using a variety of X-ray techniques. Argonne's multi-purposein situX-ray (AMPIX) cell provides reliable electrochemical cycling over extended periods owing to the uniform stack pressure applied by rigid X-ray windows and the formation of a high-fidelity hermetic seal. The suitability of the AMPIX cell for a broad range of synchrotron-based X-ray scattering and spectroscopic measurements has been demonstrated with studies at eight Advanced Photon Source beamlines to date. Compatible techniques include pair distribution function analysis, high-resolution powder diffraction, small-angle scattering and X-ray absorption spectroscopy. These techniques probe a broad range of electronic, structural and morphological features relevant to battery materials. The AMPIX cell enables experiments providing greater insight into the complex processes that occur in operating batteries by allowing the electrochemical reactions to be probed at fine reaction intervals with greater consistency (within the charge–discharge cycle and between different methodologies) with potential for new time-dependent kinetic studies or studies of transient species. Representative X-ray and electrochemical data to demonstrate the functionality of the AMPIX cell are presented.

Diffuse Reflectance FT-IR Characterization of Active Sites under Reaction Conditions: The Production of Oxygenates in the CO/H2 Reaction

1994 ◽  
Vol 48 (10) ◽  
pp. 1208-1212 ◽  
Author(s):  
J. J. Benítez ◽  
I. Carrizosa ◽  
J. A. Odriozola
Keyword(s):  
Infrared Spectra ◽  
Active Sites ◽  
Diffuse Reflectance ◽  
Reaction Conditions ◽  
In Situ Drifts ◽  
Ft Ir

The reactivity of a Lu2O3-promoted Rh/Al2O3 catalyst in the CO/H2 reaction is reported. Methane, heavier hydrocarbons, methanol, and ethanol are obtained. In situ DRIFTS has been employed to record the infrared spectra under the actual reaction conditions. The structure of the observed COads DRIFTS bands has been resolved into its components. The production of oxygenates (methanol and ethanol) has been correlated with the results of the deconvolution calculation. Specific sites for the production of methanol and ethanol in the CO/H2 reaction over a Rh,Lu2O3/Al2O3 catalyst are proposed.

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