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  • catalyst  (2)
  • effects of type of catalyst  (1)
  • silver-doped silica  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 8 (1997), S. 483-487 
    ISSN: 1573-4846
    Keywords: thick film ; interfacial polymerization ; film formation mechanism ; catalyst
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A thick silica gel film, corresponding to the glass film of 10–20 micron in thickness, has been formed at the interface between two immiscible liquids, hexane and water, using E-40, a partially polymerized silicon alkoxide, as the precursor. The film formation was possible using both acid- and base-catalyzed water, but was greatly dependent on the type of catalyst. Only the trace of a film was observed for the system catalyzed with a strong electrolyte such as HCl, HNO3 or NaOH, while a gel film, corresponding to the glass film of several to 10 micron in thickness was formed with a weak electrolyte such as ammonia, organic acid like acetic acid, citric acid, etc., of similar pH value. The direct introduction of organic base catalyst like triethylamine in hexane was much more effective than the use of ammonia water, suggesting that the polymerization of E-40 to form a gel film takes place in the organic phase, where water molecules, as well as undissociated ammonia or organic acids, can diffuse in.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 8 (1997), S. 483-487 
    ISSN: 1573-4846
    Keywords: thick film ; interfacial polymerization ; film formation mechanism ; catalyst
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A thick silica gel film, corresponding to the glass film of 10–20 micron in thickness, has been formed at the interface between two immiscible liquids, hexane and water, using E-40, a partially polymerized silicon alkoxide, as the precursor. The film formation was possible using both acid- and base-catalyzed water, but was greatly dependent on the type of catalyst. Only the trace of a film was observed for the system catalyzed with a strong electrolyte such as HCl, HNO3 or NaOH, while a gel film, corresponding to the glass film of several to 10 micron in thickness was formed with a weak electrolyte such as ammonia, organic acid like acetic acid, citric acid, etc., of similar pH value. The direct introduction of organic base catalyst like triethylamine in hexane was much more effective than the use of ammonia water, suggesting that the polymerization of E-40 to form a gel film takes place in the organic phase, where water molecules, as well as undissociated ammonia or organic acids, can diffuse in.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1573-4846
    Keywords: thick silica gel films ; interfacial polymerization ; effects of pH ; effects of type of catalyst
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The polymerization of different silicon precursors at the interface of two immiscible liquids (“organic” and “inorganic” phase) led to the formation of thick (up to 40 μm) and crack-free silica gel films. The pH of the “inorganic” phase and the type of catalyst strongly governed the rate of film formation along with the gel film properties. The preparation of thick and crack-free gel films within 24 hours of reaction time was possible for both acid-catalyzed and base-catalyzed systems in the vicinity of pH=2 and 11, respectively. The use of acetic acid as an catalyst led to gel films with a weight eight times higher than those prepared using HCl and HNO3 catalysts. The weight of formic acid-catalyzed gel films was four times higher, and the weight of citric acid-catalyzed gel films was twice as high as the mineral acid-catalyzed gel films, respectively.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-4846
    Keywords: nanoparticles ; solvent chemistry ; silica sol-gel ; silver-doped silica
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The mechanisms responsible for spontaneous silver precipitation in silver-doped sol-gel materials are identified. The chemistry of the solvent phase is found to be the critical factor in controlling this phenomenon. The addition of HCl as catalyst leads to the formation of AgCl and subsequent formation of silver upon light exposure. Another factor leading to silver precipitation is the reducing capability of methanol radicals. Silver precipitation is inhibited by simply washing out the pore solvents by a solvent exchange method.
    Type of Medium: Electronic Resource
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