ALBERT

Notes: Bismuth titanate was synthesized under hydrothermal conditions from an amorphous bismuth–titanium precursor gel. The gel was formed by mixing a bismuth acetate complex with titanium butoxide and then adding the solution dropwise into 6M NaOH. The resulting gel suspension was reacted under hydrothermal conditions at temperatures ranging from 160° to 200°C to form crystalline bismuth titanate. The gel crystallization kinetics increased with temperature, which resulted in 100% crystalline bismuth titanate in 5 h at 200°C. Wavelength-dispersive spectroscopy data indicated that sodium was incorporated into bismuth titanate during processing, and X-ray diffractometry suggested that the powder was composed of the Bi5Ti4O15 phase. Transmission electron microscopy micrographs showed that the gel particles decomposed to 100–200 nm crystalline bismuth titanate particles during hydrothermal processing.

Notes: BaxSr1-xTiO3 (BST) powders were processed at temperatures 〈100°C by reacting nanosized TiO2 powders in alkaline, aqueous solutions of BaCl2, SrCl2, and NaOH. The effects of processing variables (NaOH concentration, time, temperature, and the ratios of barium, strontium, and titanium initially in solution) on the resultant BST powder stoichiometry and solid solubility were examined. In all cases, strontium was more readily incorporated into the BST powders than barium, and the extent varied systematically with the processing variables. BST powders that were processed in solutions with a large initial excess of barium and strontium, relative to titanium, consisted of a single-phase solid solution. In contrast, BST powders that were processed in solutions with a small initial excess of barium and strontium, relative to titanium, contained a biphasic solid solution which corresponded to separate barium-rich and strontium-rich phases.

Notes: The influence of processing parameters on the growth and morphology of hydrothermally derived lead titanate (PbTiO3) powders was investigated. PbTiO3 powder was synthesized by suspending nanocrystalline powders of TiO2 in aqueous solutions of KOH and Pb(CH3COO)2·3H2O at temperatures ranging from 120° to 200°C. PbTiO3 growth initiated in the 〈100〉 exposing the (001) surfaces and resulting in a faceted platelet morphology. Particle growth proceeded by further nucleation and growth on existing (001) surfaces. Through repeated dissolution and precipitation, the platelet clusters coarsened into larger cuboidal particles. PbTiO3 particle size was controlled by either inhibiting or promoting dissolution-precipitation. Dissolution-precipitation was inhibited by lowering the KOH concentration or the reaction temperature, or maintaining an excess of lead ions in solution, while it was promoted by increasing the KOH concentration and temperature. Coarsening of PbTiO3 particles coincided with decreases in the X-ray diffraction (XRD) peak breadth, the asymmetry of lcomponent XRD reflections, and the c-axis length.

Notes: BaTiO3 thin films were processed hydrothermally on Ag-coated quartz substrates at 90°C by reacting films of titanium dimethoxy dineodecanoate (TDD) in aqueous solutions of Ba(OH)2. Two reaction sequences were used: either the TDD was reacted directly in aqueous Ba(OH)2, or the TDD was first pyrolyzed in air at temperatures ranging from 200° to 500°C before hydrothermal reaction. Depending on the processing conditions, the dielectric constant of the thin films ranged from 5 to 170, the dielectric constant increasing with increasing pyrolysis temperature. Thin film porosimetry data suggest that the improvement in film dielectric performance is related to decreases in thin film residual porosity after hydrothermal reaction.

Notes: PbTiO3 and PbTiO3/polymer thin films were synthesized from metallo-organic precursors on metallized quartz substrates. Titanium dimethoxy dineodecanoate (TDD) was spin-cast onto the substrates and converted to polycrystalline TiO2 via hydrolysis in deionized water for 5 h at 80°C. Polycrystalline PbTiO3 films were then formed by reacting the TiO2 films for 4 h at 200°C in aqueous solutions of KOH and Pb(CH3COO)2·3H2O. Low KOH concentrations suppressed film coarsening, thereby facilitating the formation of fine-grain continuous PbTiO3 films. PbTiO3/polymer thin films were processed as above after first dissolving TDD and a polystyrene/polybutadiene block copolymer in p-xylene. PbTiO3 and PbTiO3/polymer films had relative permittivities of ≈56 and 34 and dielectric strengths of ≈250 and 850 kV/cm, respectively.

Notes: The tolerance of weed-free wheat and barley to a range of herbicides (bromoxynil, methabenzthiazuron, MCPA, bromoxynil + MCPA. linuron, prometryne, diuron, 2,4-D ester and 2,4-D amine) when applied at the crop three-leaf stage, was examined over the 5-year period 1968–72. All chemicals lowered grain yields to some extent, but the variation between chemicals was greater for wheat than for barley. In both crops, methabenzthiazuron was the safest chemical causing only small (〈2·0%,) yield losses at rates up to 2·25 kg a.i./ha. At this rate of application yield losses of up to 36% were recorded for the substituted urea derivatives. Both crops had a low tolerance to 2,4-D ester and amine. Yield losses from bromoxynil, bromoxynil + MCPA and MCPA were similar, varying from 4 to 8% al 0·5 kg a.i./ha to 9–24% at 2·25 kg a.i./ha. Pertes de rendement dans le blé et l'orge provoquées, en l'absence de mauvaises herbes, par des herbicides de postlevée Pendant une période de 5 années (1968–1972) les auteurs ont examiné la résistance du béet de l'orge. Traités, en l'absence de mauvaises herbes, au stade 3 feuilles, avec une série d'herbicidcs (bromoxynil, méthabenzthiazuron, MCPA, bromoxynil-i-MCPA, linuron, prométrync. ditiron, 2,4-D ester et 2,4-D a mine). Tous ces produits ont diminué les rendements en grains dans des proportions variées, mais la variation entre produits a été plus grande pour le blé que pour l'orge. Pour les deux céréales, le méthabenzlhiazuron a été le produit le moins toxique, provotjuant seulement de faibles penes de rendement inférieurcs à 2,0%, à des doses allant jusquà 2,25 kg/m.a/ha. A cette dose d'application, des pertes de rendement allant jusquà 36% ont élé enregistrées avec des urées substituées. Les deux éréles ont manifesté uoe faible resistance au 2,4-D estr et amine. Les pertes de rendement provoquées par le bromoxynil, le bromoxynil + MCPA, et le MCPA ont été analogues, variant de 4 à 8% pour 0,5 kg/m.a./ha, jusqu’à 9 à 24% pour 2,5 kg/m.a./ha. Ertragsverluste durch Nachaufiatifherbizide in unkrautfreiem Weizen und Gerste In unkrautfreien Weizen- und Gerstebestánden wurde in fünfjáhrigen Versuthcn (1968–72) die Toleranz der beiden Arten gegenüber folgenden Herbiziden untersucht: Bromoxynil, Methabenzthiazuron, MCPA, Bromoxynil + MCPA. Linuron, Prometryn, Diuron, 2,4-D-Eister und 2,4-D-Amin- salz. Die Behandlung erfolgte jeweils im 3-Blattstadium. Alle Verbindungen erniedrigten zu einem gewissen Grad den kornertrag. Beim Weizen waren aber die Unterschiede zwischen den verschiedenen Herbiziden grösser als bei der Gerste. Methabenzthiazuron war bei Aufwandmengen bis zu 2.25 kg A.S./ha in beiden Getreidearten das sicherste Herbizid und verursachte nur geringe Ertragsdepressionen (〈2%). Bei dieser Aufwandmenge wurden bei den Harn-stoffherbiziden bis zu 36% Ertragsverlust festgestellt. Gegen 2,4-D-Ester und 2,4-D-Aminsalz waren Weizen und Gerste wenig tolerant. Die Ertragsverluste durch Bromoxynil, Bromoxynil + MCPA und MCPA waren etwa gleich und betrugen 4–8% bei 0.5 kg A.S./ha bis 9–24% bei 2,25 kg A.S./ha.