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  • 1
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Optical response due to the photo excited carrier or exciton dynamics in a one-dimensional (1D) dimethylglyoxime Pt complex [Pt(dmg)2] has been investigated by femtosecond pump–probe spectroscopy. Measurements were made at several excitation energies between the exciton state and the free electron hole pair state. Induced absorption was observed in the low-energy side of the exciton band at any excitation energy. The spectral shape of the induced absorption changed with time between 0.1 and 0.3 ps after instantaneous rise up. These results can be explained by the formation and thermalization processes of the relaxed excited state on the adiabatic potential surface. The unthermalized relaxed excited state is formed in a very short time (〈50 fs). From the Raman spectrum, the frequency of the intermolecular stretching mode along the chain was estimated to be 80 cm−1 (T∼400 fs). These facts suggest that, in contrast to other 1D systems such as polydiacetylenes (PDA) and halogen bridged mixed valence metal complexes (MX), the formation of the relaxed excited state is caused not by the stretching vibration along the 1D chain. We propose the possibility that the triggering of the primary relaxation is caused by a high frequency (〉600 cm−1) intramolecular mode which is not in the direction of the 1D chain. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 82 (1999), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Lanthanum zirconate (La2Zr2O7) was prepared by coprecipitating lanthanum nitrate and zirconyl oxychloride at pH 10, followed by ethanol washing. The initial high surface area of ∼304 m2·g−1 decreased very rapidly with increased sintering temperature and decreased to an immeasurably small value after heating at 1200°C for 15 h. The major parameters studied were phase evolution, crystallite size, porosity, surface area reduction, and shrinkage during sintering. Three temperature regions were identified based on these studies: below the crystallization temperature, between the crystallization temperature and ∼1100°C, and above 1100°C. The main contribution of surface area reduction in the region 800°–1100°C was due to surface diffusion; the main contribution above 1100°C was due to grain-boundary diffusion coupled with surface diffusion.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Alkoxide-derived boehmite precipitates were subjected to different post-precipitation treatments to obtain a peptized sol, an unpeptized slurry, and an ethanol-washed gel precipitate. These materials were dried further to obtain the corresponding gels. Changes in the surface area, porosity, and pore size with temperature and the phase-transformation behavior from gamma-alumina to alpha-alumina were studied using X-ray diffractometry, differential scanning calorimetry, and physical adsorption/desorption measurements. Gels that were obtained from the peptized sol retained the lowest porosity, in comparison to the ethanol-washed gel and the gel that was prepared from the aqueous slurry.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 80 (1997), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effects of tartaric acid that was used in sol–gel processing on specific surface area, pore-size distribution, and gel structure of sol–gel-derived silica gels were investigated. The specific surface area of silicas that were calcined at 450°C increased from ∼600 m2/g to ∼1200 m2/g as the amount of tartaric acid that was used increased. The pore-size distribution changed as the surface area increased, and only the gels that had a surface area of 930-990 m2/g showed a very sharp pore-size distribution in the mesopore range. The difference in gel structure and properties was explained in terms of the acidity of tartaric acid and the inhibition of condensation among primary particles through the coordination or adsorption of tartaric acid on the particle surface. From the thermal behavior of the gels with different features, it was concluded that gel properties are determined not only by the structure of the precursor gel but also by the surface activity. The gel with uniform mesopores gave a high surface area over a wide range of calcination temperatures.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 83 (2000), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Pure Al2O3 and different compositions of La2O3–Al2O3 samples have been prepared through coprecipitation. Even after heating at 1300°C, the compositions La2O3·11Al2O3 and La2O3·13Al2O3 had higher surface area compared to the pure Al2O3 and the La2O3·Al2O3 composition. Ethanol washing is an effective way for improving the textural stability of pure Al2O3 and La2O3–Al2O3 samples. The effect of steam on the thermal stability of La2O3·11Al2O3 has also been studied. La2O3·11Al2O3 sample is found to be stable in steam.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 19 (2000), S. 695-699 
    ISSN: 1573-4846
    Keywords: complexing-agent assisted sol-gel method ; XPS ; epoxydation ; decomposition of cumene hydroperoxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Titania containing catalysts were prepared by conventional procedures (coprecipitation, hydrogel kneading and titania precipitation) and a complexing-agent assisted sol-gel method. The effect of preparation methods on their properties and catalytic activities in the oxidation of olefins and decomposition of cumene hydroperoxide were examined. The sol-gel method gave the best dispersion of titania. In contrast, with the kneading and titania precipitation method, titania formed crystalline particles. The sol-gel catalysts are more effective for epoxydation of olefins because of the high dispersibility of Ti in them. However, the most active catalysts in the decomposition of cumene hydroperoxide are kneading ones.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-4846
    Keywords: iron oxide ; structural control ; complexing agent ; thin film ; sol-gel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The structure of iron oxide was controlled by regulating the hydrolytic polymerization of aquo iron complexes with organic polydentate ligands such as diols. Iron oxides were prepared by calcining the precursor polymers obtained from iron nitrate nonahydrate and diols. When the diols were 1,2-pentanediol, 1,2-hexanediol and 1,2-octanediol, α -Fe2O3 with corundum structure appeared exclusively or as the main crystalline phase, in spite of the amount of diol used and the calcination temperature. In the case of 1,2-decanediol and 1,2-dodecanediol, when five moles of the diols were used to one mole of iron nitrate and the calcination temperatures were below 400° C, γ -Fe2O3 with spinel structure appeared as the main phase and, when less than five moles of the diols were used, α -Fe2O3 appeared exclusively or as the main phase, irrespective of the calcination temperature. This tendency was also observed in thin films. Thus, a transparent magnetic film composed of γ -Fe2O3 could be prepared by applying a benzene solution of the iron polymer, obtained with 5 equivalents of 1,2-decanediol, on quartz and calcining the gel film at 350° C.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 1 (1994), S. 113-121 
    ISSN: 1573-4846
    Keywords: crystal structure ; complexing agent ; TiO2 ; TiO2-SiO2
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Many types of TiO2-SiO2 (Ti:Si=50:50 mol%) were prepared by the sol-gel procedure with and without 2-methyl-2, 4-pentanediol (MPD) as an organic ligand. The effect of MPD on the gel structure and the properties of the TiO2 crystals were studied by XRD and raman spectroscopy, and the effect of the sol standing time on the properties of the TiO2 crystals were also studied by XRD spectroscopy. In the gels with MPD, anatase of TiO2 appeared at approximately 580°C, and the crystal structures were similar despite the difference in the gel preparation procedure. The titania gels with MPD were presumed to be dispersed in the silica gel matrix without any Ti-O-Si bond. In the presence of MPD, the formation of titania gels is controlled and the specified TiO2 crystal is produced.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 13 (1998), S. 1027-1031 
    ISSN: 1573-4846
    Keywords: alumina-silica ; methanol conversion ; pore design ; sol-gel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Amorphous alumina-silicas were prepared from a tetra-alkoxysilane and anhydrous aluminum trichloride or an aluminum alkoxide by a sol-gel process using 2-methyl-2,4-pentanediol, pinacol, 1,2-propanediol, 2,3-butanediol or ethylene glycol as the solvent or complexing agent, and the effect of diols and alkoxy groups on the physical and chemical properties of the alumina-silicas was examined. When the diol or the alkoxy group was bulky, the alumina-silicas had relatively larger micropores, a larger pore volume and higher surface areas. In the conversion of methanol catalyzed by the alumina-silicas, the bulkier diols and alkoxides gave catalysts that produced dimethyl ether in higher yield and hydrocarbons in lower yield. Thus, when ethylene glycol was used as the diol, the best catalyst for the production of hydrocarbons, especially the production of olefins such as ethylene, propylene and butene, was obtained. Furthermore, in comparison with alumina-silica prepared by a traditional kneading process, it was found that the sol-gel alumina-silica could efficiently convert methanol to dimethyl ether and hydrocarbons, but the material prepared by kneading had a very low conversion of methanol to other compounds.
    Type of Medium: Electronic Resource
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