HRTEM observation of the monoclinic-to-tetragonal m-t) phase transition in nanocrystalline ZrO2

The orientation relations m(100) || t(001), m[001] || t[110]; m(011) || t(100), m[100] || t[001]; m(100) || t(110), m[001] || t[001]; m(013) || t(116), m[001] || t[001] (indices for the primitive tetragonal cell) have been found between the tetragonal (t) and monoclinic (m) domains during the electron irradiation-induced m-t phase transition observed in-situ with HREM within isolated zirconia nanoparticles. Geometric models of the m-t interfaces are proposed.     

Preparation of Phase-Pure M1 MoVTeNb Oxide Catalysts by Hydrothermal Synthesis—Influence of Reaction Parameters on Structure and Morphology

This work presents a detailed investigation of the preparation of MoVTeNbO _x catalysts by hydrothermal synthesis. Phase-pure synthesis of M1 has been achieved applying the metals in a molar ratio Mo/V/Te/Nb = 1/0.25/0.23/0.12. Raman, UV/Vis spectroscopy, and SEM/EDX analysis show that the elements are inhomogeneously distributed in the initial suspension that is formed after mixing the metal salts in an aqueous medium. Iso- and heteropoly anions of molybdenum, free telluric acid as well as supra-molecular polyoxometalate clusters are observed in the solution, whereas all metals have been found in the precipitate. Complete rearrangement of molecular building blocks under hydrothermal conditions is essential for formation of phase-pure materials. Optimized synthesis conditions with respect to temperature and time result in the formation of a precursor consisting of nano-structured M1 characterized by an extended periodic organization in the [001] direction and a fairly homogeneous distribution of the elements. Residual ammonium containing supra-molecular species in the precursor result in the formation of phase mixtures during the subsequent crystallization by heat treatment in inert gas. Phase-pure M1 exhibits a distinct degree of flexibility with respect to the chemical composition that becomes obvious by incorporating Nb not exclusively into pentagonal bi-pyramidal units, but also into octahedral coordinated positions as shown by EXAFS. Anisotropic growth of the needle-like M1 crystals has been observed during the final heat treatment performed at 873–923 K in inert atmosphere disclosing a potential method to control the catalytic properties of MoVTeNbO _x catalysts.     

Spatially resolved X-ray diffraction phase mapping and α → β → α transformation kinetics in the heat-affected zone of commercially pure titanium arc welds

Spatially resolved X-ray diffraction (SRXRD) is used to map the α → β → α phase transformation in the heat-affected zone (HAZ) of commercially pure titanium gas tungsten arc welds. In situ SRXRD experiments were conducted using a 180-μm-diameter X-ray beam at the Stanford Synchrotron Radiation Laboratory (SSRL) (Stanford, CA) to probe the phases present in the HAZ of a 1.9 kW weld moving at 1.1 mm/s. Results of sequential linear X-ray diffraction scans made perpendicular to the weld direction were combined to construct a phase transformation map around the liquid weld pool. This map identifies six HAZ microstructural regions between the liquid weld pool and the base metal: (1) α-Ti that is undergoing annealing and recrystallization; (2) completely recrystallized α-Ti; (3) partially transformed α-Ti, where α-Ti and β-Ti coexist; (4) single-phase β-Ti; (5) back-transformed α-Ti; and (6) recrystallized α-Ti plus back-transformed α-Ti. Although the microstructure consisted predominantly of α-Ti, both prior to and after the weld, the crystallographically textured starting material was altered during welding to produce different α-Ti textures within the resulting HAZ. Based on the travel speed of the weld, the α → β transformation was measured to take 1.83 seconds during heating, while the β → α transformation was measured to take 0.91 seconds during cooling. The α → β transformation was characterized to be dominated by long-range diffusional growth on the leading (heating) side of the weld, while the β → α transformation was characterized to be predominantly massive on the trailing (cooling) side of the weld, with a massive growth rate on the order of 100 μm/s.     

Activity and Selectivity of a Nanostructured CuO/ZrO2 Catalyst in the Steam Reforming of Methanol

Steam reforming of methanol for production of hydrogen can be carried out over copper based catalyst. In the work presented here, the catalytic properties of a CuO/ZrO₂ catalyst (8.5wt%) synthesised by a templating technique were investigated with respect to activity, long term stability, CO formation, and response to oxygen addition to the feed. The results were obtained using a fixed bed reactor and compared to a commercial methanol synthesis catalyst CuO/ZnO/Al₂O₃. It is shown that, depending on the time on stream, the temporary addition of oxygen to the feed has a beneficial effect on the activity of the CuO/ZrO₂ catalyst. After activation, the CuO/ZrO₂ catalyst is found to be more active (per copper mass) than the CuO/ZnO/Al₂O₃ system, more stable during time on stream (measured up to 250h), and to produce less CO. Structural characterisation by means of X-ray powder diffraction (XRD) and X-ray absorption spectroscopy (XAS) reveals that the catalyst (as prepared) consists of crystalline, tetragonal zirconia with small domain sizes (about 60Å) and small/disordered crystallites of CuO.     

Kinetics of Solid-State Reactions in Heterogeneous Catalysis from Time-Resolved X-Ray Absorption Spectroscopy

The potentials of X-ray absorption spectroscopy (XAS) (quantitative phase composition and average valence together with a short-range order structure analysis) combined with a time-resolution in the second range make time-resolved (TR-) XAS a powerful tool for investigating the reactivity of solids in catalysis and solid-state chemistry. General aspects of TR-XAS investigations are discussed (i.e., instrumentation, data analysis). In addition, some experiments illustrate how the kinetics of solid-state reactions in heterogeneous catalysis can be elucidated from TR-XAS studies.     

Multi-aspect detection of surface and shallow-buried unexplodedordnance via ultra-wideband synthetic aperture radar

An ultra-wideband (UWB) synthetic aperture radar (SAR) system is investigated for the detection of former bombing ranges, littered by unexploded ordnance (UXO). The objective is detection of a high enough percentage of surface and shallow-buried UXO, with a low enough false-alarm rate, such that a former range can be detected. The physics of UWB SAR scattering is exploited in the context of a hidden Markov model (HMM), which explicitly accounts for the multiple aspects at which a SAR system views a given target. The HMM is trained on computed data, using SAR imagery synthesized via a validated physical-optics solution. The performance of the HMM is demonstrated by performing testing on measured UWB SAR data for many surface and shallow UXO buried in soil in the vicinity of naturally occurring clutter     

A novel electrostatic approach to enzyme mechanisms: carbonic anhydrase as an example

A novel electrostatic approach to the manner in which enzymes catalyze reactions is developed. In this development, the author's interpretations of, and additions to, the late K. Fajans' theory of electronic structure (referred to as the Quanticule theory of chemical binding) are presented. This theory is based upon electron densities, in analogy to density functional theory. It is used to derive formulations of molecular structure, (Fajans' formulations) which show the charges of the atomic components. These charges are shown to be reduced by polarization to what are commonly referred to as partial charges. These formulations relate to the exchange of charged atomic components during reactions. The relevance of the formulations to the catalytic activity of enzymes is illustrated with carbonic anhydrase. When viewed in terms of Fajans' formulations, the active site is seen to consist of an array of charged atoms. The positive and negative charges tend to alternate. When closely positioned, these charges provide a basis for drawing atomic components of the molecules, which are exchanged in a given reaction, into the new positions. The charges are shown to be related to the binding of substrates to the enzyme and the positioning of them so that they can interact, to the reaction itself, to an essential proton transfer, and to the dissociation of the product from the enzyme. This more extensive scope of electrostatic interactions provides a more simple view of the manner in which the catalysis is accomplished. Such catalysis is consistent with a number of other proposals about enzyme mechanisms, and appears to be applicable to a large majority of enzyme-catalyzed reactions.     

In situ analysis of metal-oxide systems used for selective oxidation catalysis: how essential is chemical complexity?

The mode of operation of selective oxidation reactions is described by a series of chemical rules defining the catalyst and some reaction intermediates. In contrast to catalytic processes over metallic elements, little is known, however, about the atomistic details of selective oxidation. In particular, the participation of the subsurface region of the catalyst in the kinetically relevant elementary steps (Mars–van Krevelen mechanism) is not positively verified. Using in situ X-ray absorption techniques to study binary and ternary molybdenum oxides the present contribution shows that it is possible to tackle some of the problems in selective oxidation by direct experimental observation. The modification of the Mo–O local bonding interaction upon thermal reduction of MoO₃to MoO_3-x is illustrated. This was also found for mixed Mo–V oxides in which the chemical state of the vanadium seemed unaffected by the reaction but the surface Mo:V ratio varied substantially with the gas phase composition. It is further shown that the solid-state phase transformation between reduced and oxidised forms of molybdenum oxides occur so rapidly, that possibly relevant suboxide cannot be identified by ex situ phase analysis. Observation of the time-law of redox transformations showed that lattice oxygen is only available for selective oxidation if the associated solid-state transformation occurs in the kinetic regime of reaction control and not in that of diffusion control.