Substrate effect on the growth of iron clusters in Y zeolite

Investigation of the decomposition process and of the thermolytic products obtained from Fe(CO)5/faujasite adducts by thermogravimetric, IR-spectroscopic, Mössbauer spectroscopic and X-ray absorption measurements (EXAFS) provides evidence for a substrate effect on the growth process of iron clusters. CsY substrate increases the Fe---CO bond strength. The stabilized intermediates generated by this effect upon thermolysis at 500 K are easily oxidized to small iron(III) oxide clusters, whereas with NaY substrate to a large extent iron(O) particles are generated. The latter show Mössbauer effect and EXAFS spectra comparable to those obtained from bulk iron. An inner oxidation process is assumed to be involved in the generation of the zeolite-supported iron oxide

Monomolecular layers and thin films of silane coupling agents by vapor-phase adsorption on oxidized aluminum

Thin films of tetraethoxysilane [TEOS], (3-bromopropyl)trimethoxysilane [BPS], trimethoxyvinylsilane [VS], and 3-(tri-methoxysily1)propyl methacrylate [TPM] on oxidized aluminum surfaces have been investigated by reflection-absorption FTIR spectroscopy, ellipsometry, contact angle, and quartz crystal microbalance (QCM) measurements. Gravimetric measurements with the QCM can reveal quantitative aspects of adsorption and film formation, even for films as thin as monolayers. Adsorption of these silane coupling agents from solution typically produces multilayer films. Vapor-phase adsorption of TEOS and TPM at room temperature results in monomolecular layers. The coupling agents VS and BPS require additional heating after the vapor-phase adsorption to initiate the hydrolysis and condensation reactions necessary for the surface attachment, which produces one to three layers. For vapor adsorbed films a packing density of 4-7 molecules/nm2 was found. The data strongly suggest that the organic moieties in several of these films have a preferential orientation on the surface; they can be viewed as two-dimensional, oligomeric siloxane networks with oriented organic chains. Subsequent heating of TPM films results in structural rearrangements; heating of TEOS results in complete condensation to Si02 films

Characterization of a new iron-on-zeolite Y Fischer-Tropsch catalyst

Iron pentacarbonyl adsorbed on dry Na-Y zeolite can be oxidized at subambient temperatures into Fe203 located in the zeolite supercages (catalyst I). When catalyst I is hydrogen reduced at 575 K most of the iron has agglomerated externally to the zeolite (catalyst 11). When the iron carbonyl is thermally decomposed in vacuo at 525 K, an iron phase with a very low degree of dispersion is again obtained (catalyst 111). During a Fischer-Tropsch reaction most of the iron is transformed into a Hagg-type carbide phase, located externally to the zeolite. Catalysts I1 and 111 rapidly reach steady state and show a Schulz-Flory-type of product distribution, the Hagg carbide being the active phase. Catalyst I slowly moves to steady state and Schulz-Flory behavior. Product selectivity is only found on this catalyst during transient conditions. The physical information on the three catalysts before and after reaction was obtained with transmission electron microscopy and Mossbauer and EXAFS spectroscopies. These techniques supplied consistent and complementary evidenc

EXAFS study of nickel exchanged into zeolite Y

EXAFS and near edge spectroscopy were used to monitor changes i n Ni coordination as a function of treatment conditions after aqueous exchange into zeolite Y. Our results suggest that after calcination and dehydration under the conditions of this study, major site occupancy for Ni appears to be in the tri-coordinate exchange sites , and not i n the hexagonal prisms as suggested by previous x-ray diffraction results

EXAFS study of nickel tetracarbonyl and nickel clusters in zeolite Y

Adsorption and thermal decomposition of Ni(CO)4 in the cage system of zeolite Y have been studied with EXAFS, electron microscopy and IR spectroscopy , Ni(CO)4 is adsorbed as an intact molecule in both cation - free zeolite Y and NaY. Symmetry changes of the molecule in NaY are assigned to the formation of Na—OC-IMi bridges. Thermal treatment of the Ni(CO)4/NaY adduct leads to loss of CO concomitant with the formation of a binodal Ni phase. A major part of the forms clusters with diameter between 0.5 and about 1.5 nm, in addition to larger crystallites (5-30 nm), sticking at the outer surface of the zeolite matrix., The Ni-Ni scattering amplitude indicates increasing average particle size with increasing temperature

Towards a public analysis database for LHC new physics searches using MadAnalysis 5

We present the implementation, in the MadAnalysis 5 framework, of several ATLAS and CMS searches for supersymmetry in data recorded during the first run of the LHC. We provide extensive details on the validation of our implementations and propose to create a public analysis database within this framework.Comment: 20 pages, 15 figures, 5 recast codes; version accepted by EPJC (Dec 22, 2014) including a new section with guidelines for the experimental collaborations as well as for potential contributors to the PAD; complementary information can be found at http://madanalysis.irmp.ucl.ac.be/wiki/PhysicsAnalysisDatabas