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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 10 (1997), S. 269-282 
    ISSN: 1573-4846
    Keywords: aerogel ; zirconia ; supercritical drying ; acetic acid ; adipic acid ; oxalic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Zirconia aerogels were prepared from tetra-n-butoxy zirconium(IV) using acid catalysis with different types of mono- and dicarboxylic acids and ensuing supercritical drying of the gels either at high temperature (578 K, HT-aerogels) or by semicontinuous extraction with supercritical CO2 at low temperature (318 K, LT-aerogels). The resulting HT- and LT-aerogels were calcined in air at 573 and 773 K, respectively, and characterized by nitrogen physisorption, X-ray diffraction, Raman spectroscopy, thermal analysis, and thermal desorption of ammonia. All HT-aerogels were mesoporous and possessed a high specific surface area between ca. 90 and 170 m2·g-1 after calcination at 773 K. With oxalic acid the pore size distributions were either bimodal (R = 1) or unimodal R = 2), depending on the acid-to-alkoxide ratio, R. In contrast, the use of acetic and adipic acid, respectively, afforded bimodal pore size distributions. Generally, the crystalline part of the raw HT-aerogels prepared with acetic and adipic acid was made up of tetragonal ZrO2 with traces of monoclinic zirconia, whereas with oxalic acid at higher acid-to-alkoxide ratio (R = 2) the monoclinic phase became dominant. Calcination in air at 773 K had no influence on the phase distribution and crystallite size. With LT-aerogels, the sample prepared with the largest acetic acid-to-alkoxide ratio (R = 2) afforded the highest BET surface area (ca. 90 m2·g-1). All LT-aerogels were X-ray amorphous after extraction and calcination in air at 573 K. Crystallization resulted in the formation of tetragonal zirconia. The crystallization temperature increased with higher acetic acid-to-alkoxide ratio, whereas the crystallite size decreased.
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  • 2
    ISSN: 1572-879X
    Keywords: Enantioselective hydrogenation ; ethyl pyruvate ; Pt/Al2O3 ; cinchona alkaloids ; modifier
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The time dependence of the conversion and enantioselectivity during the hydrogenation of ethyl pyruvate has been studied over an industrial Pt/Al2O3 catalyst. Various cinchona alkaloids were used as modifier and two different modes were applied for their introduction into the reaction system. The dependence of the enantioselectivity on conversion is strongly influenced by the mode of introduction and the structure of the modifier used. The conversion dependence of the enantioselectivity is attributed to the chemical transformations of the parent alkaloid observed under hydrogenation conditions. Experimental evidence is shown for the dynamic nature of the interaction between the modifier and the catalyst.
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  • 3
    ISSN: 1572-879X
    Keywords: ethyl pyruvate ; in situ XANES ; enantioselective hydrogenation ; platinum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The adsorption of ethyl pyruvate on Pt(111) has been studied by in situ XANES measurements in the presence and absence of hydrogen. Depending on the hydrogen and ethyl pyruvate pressure, the C and O K‐edge spectra exhibit distinctly different angular dependence. Without hydrogen ethyl pyruvate is oriented preferentially perpendicular to the surface, indicating bonding via the O lone pairs. In the presence of hydrogen the mean orientation is more tilted towards the surface. Likely, ethyl pyruvate also interacts with Pt via its π system under these conditions. The observed angle‐dependent shift of the energy of the π* and σ* resonances indicates the coexistence of differently adsorbed ethyl pyruvate species. The experimental findings demonstrate the importance of the in situ approach for unraveling the adsorption mode of ethyl pyruvate in the enantioselective hydrogenation over cinchona‐alkaloid‐modified Pt.
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  • 4
    ISSN: 1572-879X
    Keywords: enantioselective hydrogenation ; Pt/alumina ; cinchonidine ; ethyl pyruvate ; protonation ; hemiketal formation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The reasons for the increase in the rate and enantiomeric excess after oxidative (aerobic) treatment of Pt/alumina in ethanol have been investigated. It is demonstrated that this treatment results in the formation of acetic acid and consequently in the protonation of the quinuclidine n1 of cinchonidine. This favours the cinchonidine-pyruvate interaction and improves enantioselectivity. In addition, the reaction rate is enhanced due to acid catalysis of the carbonyl reduction. NMR and UV measurements indicate the rapid transformation of ethyl pyruvate to the corresponding hemiketal in primary alcohols as solvents. It is shown that the possible involvement of this hemiketal (and that formed between cinchonidine and ethyl pyruvate) as an intermediate in the pyruvate hydrogenation mechanism can be excluded.
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  • 5
    ISSN: 1572-879X
    Keywords: enantioselective hydrogenation ; chiral modifier ; ethyl pyruvate ; Pt/alumina
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The enantioselective hydrogenation of ethyl pyruvate to (R)- or (S)-ethyl lactate has been studied over alumina- and carbon-supported Pt-metal catalysts modified by various heterocyclic N-compounds and substituted amides. The reactions were carried out under mild conditions in acetic acid; other solvents had a detrimental effect on enantioselectivity. An enantiomeric excess (ee) of 67% and a rate acceleration by a factor of 6, compared to the unmodified catalyst, was observed with alumina-supported Pt modified by (R)-1-(1-naphthyl)ethylamine. In contrast, carbon-supported Pd, Ru and Rh were non-selective and only little active. The studies indicated that besides naphthyl or quinolyl groups, two separate phenyl groups or one phenyl group together with two amino groups can provide a suitable anchoring of the chiral modifier on the Pt surface. The nature of interaction between the modifiers and ethyl pyruvate is briefly discussed.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 34 (1995), S. 1-9 
    ISSN: 1572-879X
    Keywords: enantioselective hydrogenation ; supercritical fluids ; ethyl pyruvate ; cinchonidine ; Pt/alumina ; CO-poisoning
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The enantioselective hydrogenation of ethyl pyruvate to (R)-ethyl lactate has been studied using gases under supercritical conditions as solvents. The catalyst was a 5 wt% Pt/alumina modified with cinchonidine. In supercritical ethane the reaction time could be reduced by a factor of 3.5 compared to toluene under similar conditions, without any loss in enantioselectivity. A further advantage of ethane is that the enantioselectivity remains high even at high catalyst/reactant ratio, which is interesting in view of a possible application of a continuous fixed-bed reactor for this reaction. A strong catalyst deactivation was observed in supercritical CO2, which is due to the reduction of CO2 on Pt as indicated by FTIR.
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  • 7
    ISSN: 1572-879X
    Keywords: Pt/Al2O3 ; promotion by tin ; modification by tin tetraalkyls ; surface organometallic complexes ; enantioselective hydrogenation ; ethyl pyruvate ; dihydrocinchonidine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The enantioselective hydrogenation of ethyl pyruvate has been studied on a Pt/Al2O3-dihydrocinchonidine catalyst promoted with different amount of tin. The surface reaction between hydrogen adsorbed on Pt and tin tetraalkyls is used for the tin introduction. This reaction leads to the formation of surface organometallic complexes (I), with SnR(4-x) moieties anchored to the platinum surface. The enantioselectivity of the Pt/Al2O3-dihydrocinchonidine catalyst is found to change only slightly upon promotion with tin, while the rate of ethyl pyruvate hydrogenation depends strongly on the amount and the form of tin introduced. The hydrogenation activity is suppressed completely at relatively low tin coverage (Sn/Pts 〈 0.06). The highest hydrogenation rate is measured over catalysts containing complex (I) (Sn/Pts = 0.025) on the platinum surface. On Sn-Pt alloy type active sites, which are formed after decomposition of (I) in hydrogen, the rate of hydrogŋation is considerably lower than on the unpromoted reference Pt/Al2O3 catalyst.
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  • 8
    ISSN: 1572-9028
    Keywords: titania-silica ; mixed oxide ; sol-gel ; aerogel ; epoxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The paper provides a short overview on the various Ti- and Si-containing epoxidation catalysts, with a focus on the development and characterisation of titania-silica mixed oxides prepared by the sol-gel-aerogel method. Titania-silica aerogels, dried by semicontinuous extraction of the solvent with supercritical CO2 at low temperature, possess high surface area, an amorphous mesoporous structure, and a rather even distribution of Ti in the silica matrix. The catalytic activities of mixed oxides, silica-supported titania and Ti-substituted molecular sieves (TS-1, Ti-Β and Ti-MCM-41) are compared in the epoxidation of 1-hexene, 1-octene, cyclohexene, cyclododecene and norbornene, based on literature data. The activities (i.e. the amount of converted olefin per unit time and catalyst weight) vary in a broad range of several orders of magnitude. It is shown that the low temperature aerogel containing 20 wt% TiO2 is superior to any other Ti- and Si-containing catalyst for the epoxidation of cyclic olefins. In the epoxidation of linear alkenes TS-1 has outstanding activity. Ti-substituted large and ultra-large pore molecular sieves require further development concerning their catalytic performance.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of porous materials 2 (1995), S. 171-183 
    ISSN: 1573-4854
    Keywords: zirconia ; sol-gel ; aerogel ; xerogel ; alcoholic solvent ; nitric acid
    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 High-surface-area zirconia aerogels with meso- to macroporosity have been prepared by an acid-catalyzed alkoxide-sol-gel route with tetrabutoxyzirconium(IV) and subsequent high-temperature supercritical drying at 578 K. The effect of solvent (ethanol, propanol, butanol, t-amylalcohol), amount of nitric acid, calcination temperature, and drying method was studied by nitrogen physisorption, X-ray diffraction, Fourier transform Raman and diffuse reflectance infrared Fourier transform spectrosopy, scanning electron microscopy, thermal analysis, and temperature-programmed desorption of NH3. After calcination in air at 573 or 773 K, the aerogels possess specific surface areas of up to 270 or 180 m2 · g−1, respectively. The use of ethanol as solvent resulted in the highest specific surface areas and pore volumes (up to 1.5 cm3 · g−1) among all samples studied, whereas bulky t-amylalcohol caused a shift of the maxima of the broad pore size distributions from 30 to 70 nm. With the corresponding xerogels, prepared via the same wet-chemical procedure but evaporatively dried at ambient temperature, butanol resulted in a maximum at 3 nm and t-amylalcohol in a bimodal pore size distribution with maxima at 3 and 15 nm. The variation of the acid-to-alkoxide ratio in the range 0.08–0.12 at a hydrolysis level of 4 did not significantly influence the structural properties of aerogels and related xerogels. In contrast to the aerogels, the xerogels had significantly lower specific surface areas and prominent microporosity. All uncalcined aerogels contained crystalline ZrO2, whereas the corresponding uncalcined xerogels were X-ray amorphous and crystallized only during calcination at 573 K. Both aerogels and xerogels possessed Brønsted-type and Lewis-type acid sites. With the xerogels, the density of acid sites on the surface was significantly lower. This behaviour is attributed to the higher amounts of organic residues which persisted in and on the xerogels up to 773 K and thus blocked the acid sites partially.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of porous materials 2 (1995), S. 325-330 
    ISSN: 1573-4854
    Keywords: zirconia ; sol-gel ; aerogel ; acetic acid ; nitric acid
    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 Zirconia aerogels have been prepared from butanolic zirconium(IV) tetra-n-butoxide diluted in ethanol via stoichiometric hydrolysis with water in ethanol. Nitric acid or acetic acid were used to modify the sol-gel process. After calcination in air at 573 K, the aerogel prepared with nitric acid possesses a specific surface area of 240 m2 · g−1 and a unimodal pore size distribution with a maximum at ca. 24 nm, whereas the use of acetic acid results in an aerogel with specific surface area of 228 m2 · g−1 and bimodal pore size distribution with maxima at 3 and 65 nm. The crystalline fractions of both aerogels are predominantly tetragonal with a small contribution of monoclinic ZrO2.
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