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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of porous materials 5 (1998), S. 127-132 
    ISSN: 1573-4854
    Keywords: mesoporous silica ; esterification ; pore size ; hydrophobicity ; silanol group
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Silanol groups in the mesoporous silica derived from a layered silicate, kanemite (NaHSi12O5 ċ3H2O), were esterified with alcohols (CnH2n+1OH n=2 , 4, and 8). Most of the silanol groups in the mesopores were modified with ethanol though some silanol groups remained after the reactions with 1-butanol and 1-octanol. With the increase in the alkyl chain lengths of the alcohols, the pore sizes of the esterified products decreased and the hydrophobicity increased.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 787-792 
    ISSN: 0268-2605
    Keywords: tetrakis(dimethylamino)titanium ; amminolysis ; precursor ; pyrolysis ; titanium nitride ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Precursors possessing Ti-N bonds were prepared by the reactions between Ti(NMe2)4 and each of three diamines H2NCH2CH2NH2, Me(H)NCH2CH2N(H)Me, HN(CH2CH2)2NH (Ti(NMe2)4:diamine = 1:2), and were converted into ceramics by pyrolysis. The reactions with H2NCH2CH2NH2 and HN(CH2CH2)2NH led to the formation of insoluble solids, whereas a soluble oil was obtained by the reaction with Me(H)NCH2CH2N(H)Me. The pyrolyses under argon gave carbon-rich Ti(N,C,O) phases,­but those under NH3- N2 resulted in the formation of Ti(N,C,O) phases with higher nitrogen contents. Despite the difference in precursor structures the pyrolysis behavior of three precursors under argon was rather similar, suggesting that the precursor obtained from Me(H)NCH2CH2N(H)Me was effectively cross-linked during pyrolysis. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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