Powder preparation and compaction behaviour of fine-grained Y-TZP

Two wet chemical preparation methods are described for yttria-doped tetragonal zirconia powders. Both methods yield powders with an extremely small crystallite size (8 nm) and a narrow size distribution. The agglomerate and aggregate structure of these powders have been investigated by several techniques. Gel precipitation from an alkoxide solution in water (ldquoalkoxiderdquo synthesis) results in a ceramic powder with irregular-shaped weak and porous agglomerates, which are built up from dense aggregates with a size of 18 nm. Gel precipitates formed from a metal-chloride solution in ammonia (ldquochloriderdquo synthesis) do not contain aggregates. Both types of agglomerate are fractured during isostatic compaction. Hydrolysis and washing under (strong) basic conditions probably decrease the degree of aggregation. The aggregate morphology and structure are key parameters in the microstructure development during sintering of a ceramic. Several characteristics of these powders are compared with those of a commerical one (Toyo Soda TZ3Y)

The pyrolytic decomposition of metal alkoxides (di-acetoxy-di-t-butoxy-silane, DADBS) during chemical vapour deposition of thin oxide films

In this study the effects of the nature of metal alkoxides on their vapour pressures and thermal decomposition chemistry are reported. The vapour pressure and the volatility of a metal alkoxide strongly depends on the steric effect of its alkoxy group.\ud \ud The thermal decomposition chemistry of one metal alkoxide (di-acetoxy-di-t-butoxy-silane, DADBS) has been studied by mass spectrometry at temperatures between 423 and 923 K. The pyrolytic products were acetic acid anhydride and 2-methyl propene. The acetic acid anhydride is formed at temperatures above 473 K and 2-methyl propene is formed above 673 K by a ß -hydride elimination mechanism. In these steps, a 6-ring intermediate is supposed to be formed. The silicon acid finally remaining is proposed to react by poly-condensation to SiO2 coatings or powder

Thick films of YSZ electrolytes by dip-coating process

Yttria stabilized zirconia (YSZ, 8% Y2O3) thick films were coated on porous Ni-YSZ substrates using the dip-coating process and a suspension with a new formulation. The suspension was obtained by addition of a polymeric matrix in a stable suspension of a commercial YSZ (Tosoh) powders dispersed in an azeotropic MEK-EtOH mixture. The green layers were densified after an optimization of the suspension composition. YSZ Tosoh particles encapsulated by a zirconium alkoxide sol and added with colloidal alkoxide precursor are used to load the suspension. The in situ growth of these colloids increases significantly the layers density after an appropriated heat treatment. The obtained films are continuous, homogeneous and 20 μm thick. Different microstructures are obtained depending on the synthesis parameters of the suspension

Effect of temperature and branching on the nature and stability of alkene cracking intermediates in H-ZSM-5

Catalytic cracking of alkenes takes place at elevated temperatures in the order of 773–833 K. In this work, the nature of the reactive intermediates at typical reaction conditions is studied in H-ZSM-5 using a complementary set of modeling tools. Ab initio static and molecular dynamics simulations are performed on different C4single bond C5 alkene cracking intermediates to identify the reactive species in terms of temperature. At 323 K, the prevalent intermediates are linear alkoxides, alkene π-complexes and tertiary carbenium ions. At a typical cracking temperature of 773 K, however, both secondary and tertiary alkoxides are unlikely to exist in the zeolite channels. Instead, more stable carbenium ion intermediates are found. Branched tertiary carbenium ions are very stable, while linear carbenium ions are predicted to be metastable at high temperature. Our findings confirm that carbenium ions, rather than alkoxides, are reactive intermediates in catalytic alkene cracking at 773 K

Structural features and reactivity of (sparteine)PdCl_2: a model for selectivity in the oxidative kinetic resolution of secondary alcohols

The chiral ligand (−)-sparteine and PdCl_2 catalyze the enantioselective oxidation of secondary alcohols to ketones and thus effect a kinetic resolution. The structural features of sparteine that led to the selectivity observed in the reaction were not clear. Substitution experiments with pyridine derivatives and structural studies of the complexes generated were carried out on (sparteine)PdCl2 and indicated that the C1 symmetry of (−)-sparteine is essential to the location of substitution at the metal center. Palladium alkoxides were synthesized from secondary alcohols that are relevant steric models for the kinetic resolution. The solid-state structures of the alkoxides also confirmed the results from the pyridine derivative substitution studies. A model for enantioinduction was developed with C1 symmetry and Cl− as key features. Further studies of the diastereomers of (−)-sparteine, (−)-α-iso- and (+)-β-isosparteine, in the kinetic resolution showed that these C_2-symmetric counterparts are inferior ligands in this stereoablative reactio

Alkoxide complexes of rhenium, niobium and tantalum

This thesis describes two major methods for preparation of new mono-, bi- and trimetallic complexes on the basis of Rhenium, Niobium and Tantalum: (1) - the electrochemical method for the synthesis of Re4O4(OEt)12 and (2) - the interaction of Rhenium heptoxide, Re2O7, with alkoxo-derivates of Niobium and/or Tantalum, M2(OR)10 for the synthesis of bi- and trimetallic complexes of common formula (M1-xM'x)4O2(OR)14(ReO4)2 (M = Nb; M' = Ta; R = Me, Et), where x = 0–1. The structures of these complexes were determined by single-crystal X-ray diffraction. The products were also characterized by IR, NMR and X-ray powder diffraction. The influence of the increasing ligand size on the solubility and stability of the complexes Re4O4(OEt)12 and M4O2(OR)14(ReO4)2 (M = Nb, Ta; R = Me, Et) has been established. The effect of the ligand and metal ion ratio on the conditions and the chemical composition of the products of thermal treatment have been investigated. Nanosized Rhenium metal particles (approximately 3 nm in diameter) were obtained from Re4O4(OEt)12 by thermal decomposition in inert atmosphere at as low temperature as 380 °C. Semi-ordered macro porous monoliths with the pore size in the range 100 – 250 nm, with the crystal structure related to the block structures of the L-modification of Ta2O5, were produced from trimetallic complexes of the common formula (Nb1-xTax)4O2(OMe)14(ReO4)2 (x = 0.3, 0.5, 0.7) via thermal decomposition in air at the temperatures ≤ 1000 °C. The thermal decomposition in dry nitrogen atmosphere provides formation of solid solutions, which possess the structures related to the block structure of the H-modification of Nb2O5 for the Niobium-rich precursors and block structure of the L-modification of Ta2O5 for Ta:Nb ≤ 1:1 at the temperatures ≤ 1000 °C