Role of Iron Carbonyls in the Inhibition of Oxygen Activation for the Oxidation of CO Catalyzed by Iron Oxide-Supported Gold

ChemPhysChem ◽  
2012 ◽  
Vol 13 (18) ◽  
pp. 4173-4179 ◽  
Author(s):  
Sergio A. Jimenez-Lam ◽  
Zenaido Martinez-Ramirez ◽  
Iván A. Santos-López ◽  
Brent E. Handy ◽  
María G. Cárdenas-Galindo ◽  
...  
Keyword(s):  
Iron Oxide ◽  
Oxygen Activation ◽  
Oxidation Of Co ◽  
Iron Carbonyls ◽  
Supported Gold

Role of gold cations in the oxidation of carbon monoxide catalyzed by iron oxide-supported gold

2006 ◽  
Vol 242 (1) ◽  
pp. 71-81 ◽  
Author(s):  
G HUTCHINGS ◽  
M HALL ◽  
A CARLEY ◽  
P LANDON ◽  
B SOLSONA ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Iron Oxide ◽  
Supported Gold ◽  
Oxidation Of Carbon Monoxide

Thermodynamic and Kinetic Investigation of the Solvent Effect on the Oxidation of [Co(en)2SCH2COO]+ with S2O82- In Water-Methanol and Water-tert-Butyl Alcohol Mixtures

1993 ◽  
Vol 58 (5) ◽  
pp. 1001-1006 ◽  
Author(s):  
Oľga Vollárová ◽  
Ján Benko
Keyword(s):  
Transfer Functions ◽  
Activation Parameters ◽  
Butyl Alcohol ◽  
Oxidation Of Co ◽  
Kinetics Of Oxidation ◽  
Tert Butyl ◽  
Tert Butyl Alcohol ◽  
Alcohol Mixtures ◽  
Kinetics Of

The kinetics of oxidation of [Co(en)2SCH2COO]+ with S2O82- was studied in water-methanol and water-tert-butyl alcohol mixtures. Changes in the reaction activation parameters ∆H≠ and ∆S≠ with varying concentration of the co-solvent depend on the kind of the latter, which points to a significant role of salvation effects. The solvation effect on the reaction is discussed based on a comparison of the transfer functions ∆Ht0, ∆St0 and ∆Gt0 for the initial and transition states with the changes in the activation parameters accompanying changes in the CO-solvent concentration. The transfer enthalpies of the reactant were obtained from calorimetric measurements.

scholarly journals Role of hydration and micellar shielding in tuning the structure of single crystalline iron oxide nanoparticles for designer applications

Nano Select ◽  
2021 ◽  
Author(s):  
Ramis Arbi ◽  
Amr Ibrahim ◽  
Liora Goldring‐Vandergeest ◽  
Kunyu Liang ◽  
Greg Hanta ◽  
...  
Keyword(s):  
Iron Oxide ◽  
Iron Oxide Nanoparticles ◽  
Oxide Nanoparticles ◽  
Single Crystalline

scholarly journals Dynamics of Oxidation of Reduced Forms of CO2 under Electrochemical and Open-Сircuit Conditions on Polycrystalline Pt in H2CO3

Metals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 274
Author(s):  
Alexander V. Smolin ◽  
Мikhail N. Mikhailov ◽  
Aleksey F. Gadzaov ◽  
Leonid M. Kustov
Keyword(s):  
Quantum Chemical ◽  
Preliminary Analysis ◽  
Oxidation Reaction ◽  
Density Functional ◽  
Oxidation Process ◽  
Open Circuit ◽  
Organic Substances ◽  
Oxidation Of Co ◽  
Reduced Forms

The problem of identifying correlations between catalytic and electrocatalytic processes is one of the fundamental problems of catalysis among “simple” organic substances, and the oxidation of CO and rCO2 is of great interest, since CO and CO2 are considered in pairs both during catalytic and electrocatalytic transformations. In the case of electrocatalysis, this analysis is important in the study of fuel cells. In this paper, we studied the correlation between the oxidation of reduced forms of CO2 (rCO2) under potentiodynamic-galvanoctatic electrochemical and open-circuit conditions of measurements on polycrystalline (pc)Pt in H2CO3. Periodic oscillations are revealed at the oxidation of Had and rCO2 on (pc)Pt. Quantum chemical calculations were carried out on the Pt13 cluster in order to identify the mechanisms of the rCO2 oxidation reaction. The correspondence in the energy parameters of the oxidation process of rCO2 under open-circuit conditions and electrochemical conditions is shown. The preliminary analysis of the system using density functional (DFT) calculations is carried out and the most stable systems that are based on Pt13 are found, namely rOH-Pt13-(CO)n, rOH-Pt13-(COH) and rOH-Pt13-(rCOOH). OH• species was chosen as the most likely candidate for the role of the oxidant for rCO2. Preliminary calculations for the expected reactions were carried out, and the optimal PES is revealed.

GLASS STABILITY EFFECT OF IRON OXIDE ADDED TO ALKALINE EARTH BORATE GLASSES

2007 ◽  
Vol 21 (05) ◽  
pp. 731-736
Author(s):  
V. SIMON ◽  
P. RIEDL ◽  
E. TATARU
Keyword(s):  
Iron Oxide ◽  
Short Range ◽  
Alkaline Earth ◽  
Structural Changes ◽  
Opposite Effect ◽  
Glass Stability ◽  
Intermediate Range Order ◽  
Alkaline Earths ◽  
Stability Effect

Glass stability and the structural role of iron oxide in x Fe 2 O 3(100-x)[ B 2 O 3– MO ] systems ( M=Ca , Sr or Ba , 0≤x≤30 mol%) were estimated from differential thermal analysis. The results suggest structural changes characteristic for the transition from short range to intermediate range order as the cationic field strength of the alkaline earths increases. In contrast, the iron addition has an opposite effect and determines a higher glass stability of these systems.

scholarly journals Inverse single-site Fe1(OH)X/Pt(111) model catalyst for preferential oxidation of CO in H2

Nano Research ◽  
2021 ◽  
Author(s):  
Chunlei Wang ◽  
Heloise Tissot ◽  
Markus Soldemo ◽  
Junling Lu ◽  
Jonas Weissenrieder
Keyword(s):  
Iron Oxide ◽  
Iron Oxide Nanoparticles ◽  
Redox Properties ◽  
Model Catalyst ◽  
Single Site ◽  
Oxide Nanoparticles ◽  
Preferential Oxidation ◽  
Oxidation Of Co ◽  
Reaction Conditions ◽  
Preferential Oxidation Of Co

AbstractInverse oxide/metal model systems are frequently used to investigate catalytic structure-function relationships at an atomic level. By means of a novel atomic layer deposition process, growth of single-site Fe1Ox on a Pt(111) single crystal surface was achieved, as confirmed by scanning tunneling microscopy (STM). The redox properties of the catalyst were characterized by synchrotron radiation based ambient pressure X-ray photoelectron spectroscopy (AP-XPS). After calcination treatment at 373 K in 1 mbar O2 the chemical state of the catalyst was determined as Fe3+. Reduction in 1 mbar H2 at 373 K demonstrates a facile reduction to Fe2+ and complete hydroxylation at significantly lower temperatures than what has been reported for iron oxide nanoparticles. At reaction conditions relevant for preferential oxidation of CO in H2 (PROX), the catalyst exhibits a Fe3+ state (ferric hydroxide) at 298 K while re-oxidation of iron oxide clusters does not occur under the same condition. CO oxidation proceeds on the single-site Fe1(OH)3 through a mechanism including the loss of hydroxyl groups in the temperature range of 373 to 473 K, but no reaction is observed on iron oxide clusters. The results highlight the high flexibility of the single iron atom catalyst in switching oxidation states, not observed for iron oxide nanoparticles under similar reaction conditions, which may indicate a higher intrinsic activity of such single interfacial sites than the conventional metal-oxide interfaces. In summary, our findings of the redox properties on inverse single-site iron oxide model catalyst may provide new insights into applied Fe-Pt catalysis.

Role of Hydroxyl Groups in Low-Temperature CO Catalytic Oxidation over Zn4Si2O7(OH)2 Nanowire-Supported Gold Nanoparticles

2018 ◽  
Vol 122 (44) ◽  
pp. 25456-25466 ◽  
Author(s):  
Jing-Jing Li ◽  
Bao-Lin Zhu ◽  
Gui-Chang Wang ◽  
Zun-Feng Liu ◽  
Wei-Ping Huang ◽  
...  
Keyword(s):  
Gold Nanoparticles ◽  
Low Temperature ◽  
Catalytic Oxidation ◽  
Hydroxyl Groups ◽  
Co Catalytic Oxidation ◽  
Supported Gold Nanoparticles ◽  
Supported Gold
Sign in / Sign up

Export Citation Format

Share Document