PubMed · 14381313
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A G ZUPKO, A CORAN. 1955. A note on a simple universal fluid drop counter.. https://doi.org/10.1002/jps.3030440623
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Hierarchically porous inorganic nanocomposites have been synthesized combining interconnected macropores and mesopores with a high loading of site-isolated gold nanoparticles.
Most of the first-row transition-metal oxides, M(A)O(B) (M = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn) were examined by static secondary ion mass spectrometry (s-SIMS) and laser ablation/ionization Fourier transform ion cyclotron resonance mass spectrometry (LA-FTICRMS). Positive and negative ions show strong correlation between the studied oxide and the detected cluster ions. Specific M(x)O(y) (+/-) species were systematically observed with both MS techniques for each investigated M(A)O(B) transition-metal oxide. Moreover, the ion composition and ion distribution are greatly dependent on the ionization technique. Laser ablation (LA)/ionization leads to larger cluster ions (ionic species with nearly hundred atoms were in particular detected for Sc2O3 and Y2O3 oxides), whereas hydrogenated, dihydrogenated, and sometimes trihydrogenated species were observed in s-SIMS. However, the ion distribution for a given M(x)O(y) (+/-) ion series (i.e. ions including the same number of metal atoms M) generally presented important similarities in both techniques.Finally, it was demonstrated that the chemical state of metal atoms in the observed ionic species is closely dependent on the metal electronic valence shell. High valence states (+III, +IV, +V, and +VI) are favored for metals with a less-than-half full valence shell configuration, whereas for other first-row transition metals (manganese, iron, cobalt, nickel, copper and zinc) lower metal valence states (0, +I or, +II) are involved.
A room-temperature sol-gel-based process was used to produce by direct synthesis talc-like organosilicates having hexadecyl or aminopropyl groups pending in the interlayer space. Thermal analyses, Fourier transform infrared and 13C/29Si solid-state nuclear magnetic resonance spectroscopies confirmed the presence of organic moieties bonded to the inorganic network. Exfoliation of these organoclays in polar solvents such as water for the positively charged magnesium phyllo(aminopropyl)silicate, and in low polar solvents such as toluene and chloroform for hydrophobic magnesium phyllo(hexadecyl)silicate, was investigated by TEM. The ability of these layered magnesium organosilicates to exfoliate in appropriate solvents was exploited for the preparation of transparent self-supporting films and ordered macroporous networks using by latex colloidal crystal templates.