0000000000214408

AUTHOR

O. Bertrand

Interaction of oxygen with Mo(100), Mo(110), and Mo(111) surfaces. RHEED and AES analyses of the molybdenum oxide nucleation and growth

Abstract A study of the nucleation and growth of MoO 3 generated by interaction of oxygen with Mo(100), Mo(110), and Mo(111) single crystalline surfaces is investigated at high oxygen pressure (10 4 Pa) and low temperature (620 to 820 K). The results of RHEED and AES analyses prove that under these oxidation conditions, MoO 3 nucleates directly from the metal without intermediate formation of MoO 2 or nonstoichiometric molybdenum oxide such as Mo 4 O 11 . The structure and orientation of MoO 3 nuclei are characterized in relation with the parent molybdenum surface. On the Mo(110) and Mo(111) surfaces, which are faceting, the nucleation and growth of MoO 3 takes place by successive structura…

research product

Gravimetric and FTIR study of the interaction of tetramethylethylene on a MFI zeolite

The adsorption of tetramethylethylene on a high siliceous ZSM-5 zeolite was performed by thermogravimetry, in situ FTIR spectroscopy and molecular dynamics simulation. Sorption and spectroscopic data were analysed as a function of loading and compared with molecular dynamics simulated results to characterize the adsorption process. The isotherm at 298 K does not show any deviation from the type I behaviour. The presence of admolecules in micropores does not or weakly affect zeolite framework vibration bands but induces an additional band at around 1715 cm−1 mainly due to a contribution of the microporous surface of the adsorbent. A confinement effect of the adsorbate is characterized during…

research product

Superficial oxidation of molybdenum at high pressure and low temperature: RHEED and AES analyses of the molybdenum oxide formation

Abstract Numerous studies relate to the interaction of the molybdenum surface with oxygen at low pressure and high temperature. They give results about oxygen chemisorption, surface facetting and the epitaxial formation of MoO 2 crystallites. This work deals with the interaction of Mo(100), Mo(110) and Mo(111) surfaces with oxygen at high pressure (10 4 Pa) and low temperature (620–820 K). RHEED and AES analyses results prove that, in these oxidation conditions: MoO 2 and non-stoichiometric molybdenum oxide such as Mo 4 O 11 are not evidenced in any of the molybdenum oxidation steps. The MoO 3 phase nucleates directly from any Mo surface. The structure and orientation of MoO 3 nuclei are ch…

research product

Characterization and utilization of MFI zeolites and MCM-41 materials for gaseous pollutant adsorption

Physisorption of n-hexane, trichloroethylene, tetrachloroethylene, carbon and nitrogen oxides on a microporous ZSM-5 (Si/Al=339) zeolite and an amorphous mesoporous MCM-41 (Si/Al=∞) sample was examined by isothermal thermogravimetry, manometry and calorimetry to evaluate the feasibility of using these porous materials for gaseous pollutant adsorption at room temperature. The adsorbents showed very interesting adsorption properties for hydrocarbons. ZSM-5 exhibited the strongest adsorption affinity and MCM-41 showed the largest adsorption capacity. Another main feature in this work was to observe a stepped-isotherm for the adsorption of C2Cl4 on ZSM-5. Such a substep located at very low rela…

research product

Differential calorimetric enthalpies of adsorption ofp-xylene andm-xylene on y faujasites at 25°C

The differential enthalpies of adsorption ofp-xylene andm-xylene on NaY, KY and BaY zeolites were measured by isothermal calorimetry coupled with isothermal volumetry at 25‡C. Whatever the zeolite, the enthalpies of adsorption ofp-xylene andm-xylene at low filling were of the same order of magnitude. They did not show significantly the effect of the dipolar moment ofm-xylene. Their absolute values varied in the sequence

research product

Structural Signatures of Type IV Isotherm Steps:  Sorption of Trichloroethene, Tetrachloroethene, and Benzene in Silicalite-I

We have investigated by in situ neutron diffraction the structural properties of C2HCl3, C2Cl4, and C6D6 sorbed phases in silicalite-1. Our motivation is to correlate the structure of these three confined species to the fact that their adsorption isotherms are characterized by no step, one step, and two steps, respectively. From our detailed neutron diffraction investigation, we deduce that the adsorption isotherm steps are not signatures of phase transitions but are correlated to the different adsorption stages observed during the silicalite-1 loading. For C6D6, such a loading is a three stage process (the C6D6 molecules fill successively, the intersections, then the straight channels and …

research product

t-Curves for n-Hexane

The adsorption and desorption isotherms of n-hexane on powdered alumina and silica have been studied at 25°C over a wide range of relative pressures. Two t-curves for pore structure analysis are proposed, one for alumina (C = 12) and the second for silica (3 ≤ C ≤ 9). The statistical thickness t of the adsorbed n-hexane layer has been drawn as a function of the relative pressure assuming a maximal thickness of 0.55 nm and a mean thickness of 0.42 nm for the monolayer. The results are discussed in relation to previous published data.

research product

Structural variations as a function of surface adsorption in nanostructured particles

Macroscopic (adsorption isotherm and micro-calorimetry measurement) and microscopic (in situ X-ray diffraction and IR spectroscopy) approaches were used to study the influence of water adsorption on γ-Fe 2 O 3 nanoparticles. A nonmonotonic variation of γ-Fe 2 O 3 lattice parameter is revealed when the relative water pressure (p/p 0 ) increases from 0.03 to 0.96 with a maximum deviation for p/p 0 0.1. With IR spectroscopy, similar results were observed since a modification of γ-Fe 2 O 3 structural bands has been shown. In situ investigations as well as thermodynamics considerations lead to one important conclusion: the variation of the lattice parameter is in relation with the strains induce…

research product

Preparation and characterization of activated carbon from date stones by physical activation with steam

Abstract Activated carbons are produced from wastes of Algerian date stones by pyrolysis and physical activation in the presence of water vapor into a heated fixed-bed reactor. The effect of pyrolysis temperature and activation hold time on textural and chemical surface properties of raw date stones and carbon materials produced are studied. As expected, the percentage yield decreases with increase of activation temperature and hold time. The characterization of carbon materials is performed by scanning electron microscopy (SEM). X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and nitrogen adsorption (BET). Results show the presence of cellulose and hemicellulose in …

research product

Preparation and characterization of activated carbon from date stones by physical activation with steam.

International audience

research product