Temperature dependence of co-adsorption of carbon monoxide and water on highly dispersed Pt/C and PtRu/C electrodes studied by in-situ ATR-FTIRAS

2008 ◽  
Vol 53 (23) ◽  
pp. 6928-6937 ◽  
Author(s):  
M. Watanabe ◽  
T. Sato ◽  
K. Kunimatsu ◽  
H. Uchida
Keyword(s):  
Carbon Monoxide ◽  
Temperature Dependence ◽  
Co Adsorption ◽  
Highly Dispersed

Mössbauer and Exafs Study of 57Fe Labelled Pt/SiO2 Catalysts

1987 ◽  
Vol 111 ◽  
Author(s):  
J. A. Sawicki ◽  
J. H. Rolston ◽  
S. R. Julian ◽  
T. Tyliszczak ◽  
K. D. McCrimmon
Keyword(s):  
Carbon Monoxide ◽  
Nitrate Solution ◽  
Ferric Nitrate ◽  
Ambient Temperatures ◽  
Highly Dispersed ◽  
Exafs Study ◽  
Microstructural Studies ◽  
Ferric Nitrate Solution ◽  
Absorption Measurements

AbstractSpecimens of highly dispersed Pt/Silicalite catalyst, decorated with 57Fe by impregnation in aqueous ferric nitrate solution, have been studied after decoration, and various pretreatments including exposure to carbon monoxide, by in situ Mössbauer spectroscopy. The form of Pt was followed by EXAFS analysis near the Pt LIII edge. The microstructural studies were combined with CO chemisorption and infrared absorption measurements. It is observed that iron in Pt clusters is very reactive even at ambient temperatures and that the interaction of Fe with CO is strongly accelerated by platinum.

Temperature Dependence of Double Shockley Stacking Fault Behavior in Nitrogen-Doped 4h-Sic Studied by In-Situ Synchrotron X-Ray Topography

2020 ◽  
Author(s):  
Fumihiro Fujie ◽  
Shunta Harada ◽  
Kenji Hanada ◽  
Hiromasa Suo ◽  
Haruhiko Koizumi ◽  
...  
Keyword(s):  
Temperature Dependence ◽  
Stacking Fault ◽  
X Ray ◽  
Nitrogen Doped ◽  
Fault Behavior

A topological quantum-chemical study of the chemisorption of carbon monoxide on the fcc (112) surfaces of Ni, Pt, Pd, Rh, and Ir

1990 ◽  
Vol 55 (8) ◽  
pp. 1907-1919
Author(s):  
Jiří Pancíř ◽  
Ivana Haslingerová
Keyword(s):  
Carbon Monoxide ◽  
Quantum Chemical ◽  
Co Adsorption ◽  
Quantum Chemical Study ◽  
Chemical Study ◽  
Dissociative Chemisorption ◽  
Frontier Orbitals ◽  
Surface Sites ◽  
Charged Surfaces ◽  
Topological Quantum

A semiempirical quantum-chemical topological method is applied to the study of the fcc (112) surfaces of Ni, Pt, Pd, Rh, and Ir and the nondissociative as well as dissociative chemisorption of carbon monoxide on them. On Ni, dissociative chemisorption is preferred to linear capture, whereas on Pd and Pt, linear capture is preferred although dissociative chemisorption is also feasible. On Rh and, in particular, on Ir, dissociative chemisorption is energetically prohibited. The high dissociative ability of the Ni surface can be ascribed to a rather unusual charge alteration and to the degeneracy of the frontier orbitals. Negative charges at the surface level are only found on the Ni and Pt surfaces whereas concentration of positive charges is established on the Rh and Ir surfaces; the Pd surface is nearly uncharged. Metals with negatively charged surfaces seem to be able to dissociate molecules of carbon monoxide. It is demonstrated that CO adsorption can take place on all metal surface sites, most effectively in the valley of the step. In all the cases studied, the attachment to the surface is found to be energetically more favourable for the carbon than for the oxygen.

Adsorption of Carbon Monoxide on Pd/SiO2/Si(111) Studied by Core-Level Photoemission

1998 ◽  
Vol 63 (11) ◽  
pp. 1793-1802 ◽  
Author(s):  
Zdeněk Bastl ◽  
Tomáš Šarapatka
Keyword(s):  
Carbon Monoxide ◽  
Photoelectron Spectroscopy ◽  
Co Adsorption ◽  
Charge Balance ◽  
Adsorption Activity ◽  
Chemical States ◽  
Adsorbed Co ◽  
Pd Clusters ◽  
Almost All ◽  
P Type

X-Ray photoelectron spectroscopy (XPS) has been used to study the adsorption of carbon monoxide on Pd dispersed on oxidized Si(111) surface. A fraction of the deposited Pd diffusing at room temperature to the SiO2/Si interface increases with decreasing SiO2 thickness. For oxide layers thinner than ≈1 nm, almost all deposited Pd diffuses to SiO2/Si interface forming there Si silicide. Consequently, the amount of adsorbed CO is dependent on the thickness of the thermally grown SiO2 layer. Two different chemical states of adsorbed carbon atoms, the population of which depends on the amount of the Pd deposited, are observed in the C (1s) spectra of adsorbed CO. Adsorption activity of Pd clusters does not depend on whether n- or p-type Si is used. Comparison of the experimental Pd/CO concentration ratios with those calculated assuming several different modes of the Pd growth on SiO2/Si points to the pseudo-Stranski-Krastanow mode (flat clusters with incomplete condensation of the first layer) at 300 K. Changes in charge balance across the Pd/SiO2/Si interface caused by CO adsorption are discussed in terms of the surface photovoltage effect and work function variation.

scholarly journals Enhanced Tensile Strength of Monolithic Epoxy with Highly Dispersed TiO2-Graphene Nanocomposites

2021 ◽  
Vol 5 (7) ◽  
pp. 191
Author(s):  
Yanshuai Wang ◽  
Siyao Guo ◽  
Biqin Dong ◽  
Feng Xing
Keyword(s):  
Tensile Strength ◽  
Epoxy Resin ◽  
Mechanical Performance ◽  
Chemical Properties ◽  
High Mechanical Property ◽  
Graphene Nanocomposites ◽  
Highly Dispersed ◽  
Dispersion State ◽  
Physical And Chemical

The functionalization of graphene has been reported widely, showing special physical and chemical properties. However, due to the lack of surface functional groups, the poor dispersibility of graphene in solvents strongly limits its engineering applications. This paper develops a novel green “in-situ titania intercalation” method to prepare a highly dispersed graphene, which is enabled by the generation of the titania precursor between the layer of graphene at room temperature to yield titania-graphene nanocomposites (TiO2-RGO). The precursor of titania will produce amounts of nano titania between the graphene interlayers, which can effectively resist the interfacial van der Waals force of the interlamination in graphene for improved dispersion state. Such highly dispersed TiO2-RGO nanocomposites were used to modify epoxy resin. Surprisingly, significant enhancement of the mechanical performance of epoxy resin was observed when incorporating the titania-graphene nanocomposites, especially the improvements in tensile strength and elongation at break, with 75.54% and 176.61% increases at optimal usage compared to the pure epoxy, respectively. The approach presented herein is easy and economical for industry production, which can be potentially applied to the research of high mechanical property graphene/epoxy composite system.

Support and Gas Environment Effects on the Preferential Oxidation of Carbon Monoxide over Co3O4 Catalysts Studied in situ

2021 ◽  
pp. 120450
Author(s):  
Thulani M. Nyathi ◽  
Mohamed I. Fadlalla ◽  
Nico Fischer ◽  
Andrew P.E. York ◽  
Ezra J. Olivier ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Preferential Oxidation ◽  
Environment Effects ◽  
Gas Environment ◽  
Oxidation Of Carbon Monoxide

scholarly journals Removal of Cd(II) from Micro-Polluted Water by Magnetic Core-Shell Fe3O4@Prussian Blue

Molecules ◽  
2021 ◽  
Vol 26 (9) ◽  
pp. 2497
Author(s):  
Xinxin Long ◽  
Huanyu Chen ◽  
Tijun Huang ◽  
Yajing Zhang ◽  
Yifeng Lu ◽  
...  
Keyword(s):  
Prussian Blue ◽  
Co Adsorption ◽  
Magnetic Core ◽  
Diameter Distribution ◽  
Polluted Water ◽  
Core Shell ◽  
Freundlich Model ◽  
Rate Limiting Step ◽  
Rate Limiting

A novel core-shell magnetic Prussian blue-coated Fe3O4 composites (Fe3O4@PB) were designed and synthesized by in-situ replication and controlled etching of iron oxide (Fe3O4) to eliminate Cd (II) from micro-polluted water. The core-shell structure was confirmed by TEM, and the composites were characterized by XRD and FTIR. The pore diameter distribution from BET measurement revealed the micropore-dominated structure of Fe3O4@PB. The effects of adsorbents dosage, pH, and co-existing ions were investigated. Batch results revealed that the Cd (II) adsorption was very fast initially and reached equilibrium after 4 h. A pH of 6 was favorable for Cd (II) adsorption on Fe3O4@PB. The adsorption rate reached 98.78% at an initial Cd (II) concentration of 100 μg/L. The adsorption kinetics indicated that the pseudo-first-order and Elovich models could best describe the Cd (II) adsorption onto Fe3O4@PB, indicating that the sorption of Cd (II) ions on the binding sites of Fe3O4@PB was the main rate-limiting step of adsorption. The adsorption isotherm well fitted the Freundlich model with a maximum capacity of 9.25 mg·g−1 of Cd (II). The adsorption of Cd (II) on the Fe3O4@PB was affected by co-existing ions, including Cu (II), Ni (II), and Zn (II), due to the competitive effect of the co-adsorption of Cd (II) with other co-existing ions.

scholarly journals Non-monotonic magnetic anisotropy behavior as a function of adsorbate coverage in Fe ultrathin films near the spin reorientation transition

2021 ◽  
Author(s):  
A. Quesada ◽  
G. Chen ◽  
A. T. N'Diaye ◽  
P. Wang ◽  
Y. Z. Wu ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Magnetic Anisotropy ◽  
Ultrathin Films ◽  
Co Adsorption ◽  
Spin Reorientation ◽  
Spin Reorientation Transition ◽  
Out Of Plane

Carbon monoxide (CO) adsorption on ultrathin fcc Fe films is known to result in the rotation of magnetization from out-of-plane to in-plane.

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