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  • sol-gel  (85)
  • Binding Sites  (61)
  • Springer  (85)
  • American Association for the Advancement of Science (AAAS)  (61)
  • Elsevier
  • 2020-2024
  • 1995-1999  (146)
  • 1997  (146)
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  • Springer  (85)
  • American Association for the Advancement of Science (AAAS)  (61)
  • Elsevier
  • Wiley-Blackwell  (7)
Years
  • 2020-2024
  • 1995-1999  (146)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 48 (1997), S. 989-996 
    ISSN: 1572-8943
    Keywords: sol-gel ; TG ; thermal decomposition ; Y-Ba-Cu superconductors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A precursor of Y-Ba-Cu oxides was prepared by a modified alkoxide sol-gel method and its thermal decomposition in air was studied by on-line coupled TG-FTIR and High Resolution Thermogravimetric measurements. A continuous more or less stepwise weight loss was observed between room temperature and 600°C at which all organic compounds had evolved and were progressively oxidized as the temperature increased leaving only Y and Cu oxides and bariumcarbonate. Between 700 and 800°C a final weight loss was observed due to the decomposition of bariumcarbonate into oxide.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 48 (1997), S. 1051-1067 
    ISSN: 1572-8943
    Keywords: reaction mechanisms ; sol-gel ; superconductors ; thermoanalytical techniques
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The high temperature superconducting compound YBa2Cu3O72212;δ (Y-123) is synthesised by sol-gel process using various precursors viz., acetate, acetate-citrate, nitrate-citrate and acrylamide. The phase purity of the final product depends on the homogeneity of the gels which intern depends on the bonding of the metal ions in the gels. The samples prepared by acrylamide and nitrate-citrate gel routes yielded phase pure Y-123 compound with better superconducting properties. The mechanism of formation of Y-123 in all these four gel routes is established by characterising the gels and intermediate phases using TG, DTA and XRD techniques. Kinetic analysis is carried out on the mass loss data using the method proposed by Phadni's and Deshpande. Avrami-Erofeev nuclei growth in case of acrylamide, diffusion controlled process in nitrate-citrate and phase boundary reaction mechanisms in case of acetate-citrate gels are found to be responsible for the formation of Y-123 phase.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 50 (1997), S. 105-115 
    ISSN: 1572-8943
    Keywords: BiSCCO synthesis ; fluorine substitution ; sol-gel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Sol-gel citrate technology was used to prepare BiSCCO 2223 and 2212 superconducting phases. Fluorine in the initial mixture was shown to enhance considerably formation of the 2223 phase. Fluorine substitution of up to three F atoms per Bi(Pb)SCCO 2223 formula was achieved by treatment of the sample in 80 Torr ClF3 atmosphere. A number of experimental methods have been used to characterize the samples and to trace the phase transformations in the sol-gel process: DTA/TG, XRD, atomic absorption, potentiometry with fluoride selective electrode, magnetic susceptibility measurements.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 10 (1997), S. 309-316 
    ISSN: 1573-4846
    Keywords: lactate dehydrogenase ; sol-gel ; biosensor ; lactic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Physical adsorption and physical entrapment techniques have been utilized for the immobilization of lactate dehydrogenase (LDH) on tetraethylorthosilicate (TEOS) derived sol-gel films. The enzyme (LDH) activity has been assayed as a function of time, temperature, pH and pyruvate concentration. The results of photometric measurements used for monitoring the reaction yield a response time of about 1 min, linearity over a concentration range of 0–1.5 × 10-3 M and detection limit of 5 × 10-5 M. The TEOS sol-gel films containing LDH have been found to be stable for about 30 days at temperatures 4 to 10°C.
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  • 5
    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.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 8 (1997), S. 83-88 
    ISSN: 1573-4846
    Keywords: sol-gel ; gelation modelling ; TiO2 gels ; simulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract We present here an experimental and numerical study of the chemical and aggregative mechanisms for titanium alkoxide in a reverse micellar medium. NMR experiments were done to study the first step of the sol-gel process: hydrolysis of titanium isopropoxide. Light and X-ray scattering experiments were then conducted to characterize the clustering of aggregates and aggregation kinetics. Fractal dimension, measured by U.S.A.X.S., varies with the hydrolysis ratio and the hydration of the surfactant. This evolution was explained by polydispersity of the hydrolysis which depends on the surfactant concentration. This hypothesis was tested through a numerical simulation of irreversible aggregation using a chemically limited aggregation model. The hydrolyzed sites are distributed among the monomers by a random procedure governed by a polydispersity parameter p , varying from 0 to 1. The total number of hydrolyzed sites is governed by a parameter q belonging to the interval [0, 1]. The p -q evolution of the fractal dimension coincides rather well with the experimental data in all the region of the two dimensional phase space.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 8 (1997), S. 107-110 
    ISSN: 1573-4846
    Keywords: sol-gel ; zinc aluminate ; spinel structure ; catalyst support
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract ZnAl2O4 was prepared by hydrolyzing a mixture of aluminum alkoxide with zinc nitrate dissolved in hexylene glycol and calcining at 800°C. The results are compared with those obtained by wet mixing and coprecipitation. The sol-gel method produces solids whose surface areas and pore volumes are 100% larger and with a more homogeneous pore size distribution.
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  • 8
    ISSN: 1573-4846
    Keywords: mullite ; organic ligand ; hydrolytic polymerization ; sol-gel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The preparation of mullite by the sol-gel method using organic polydentate ligands and the effect of the raw materials and organic polydentate ligands on the formation of mullite were investigated. Two series of samples were prepared using tetraethoxyorthosilicate (TEOS) and aluminum nitrate nonahydrate, or dibutoxyethylacetoacetatoaluminum (Al(OBu)2(AcAcEt)) as the silica and alumina sources, respectively, and using ethylene glycol (EG), 1,3-propanediol (PD), 1,3-butanediol (BD), 2-methyl-2, 4-pentanediol (MPD), diethlene glycol monoethyl ether (DEME) and ethoxyethanol as the ligands. When the alumina source was aluminum nitrate nonahydrate, mullite was apt to appear in the order of EG 〉 PD 〉 MPD. When Al(OBu)2(AcAcEt) was the alumina source, the tendency toward the appearance of mullite crystalline phase was EG 〉 BD 〉 DEME 〉 MPD. Between the two alumina sources, aluminum nitrate nonahydrate gave mullite much easier than Al(OBu)2(AcAcEt). These relationships were discussed from the viewpoints of the coordination ability of the ligands and the miscibility between the silica and alumina.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 9 (1997), S. 279-283 
    ISSN: 1573-4846
    Keywords: AgTCNQ ; photochromism ; sol-gel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Preparation and photochromic behavior of ormosil containing encapsulated AgTCNQ molecules were studied in this paper. The ormosil resulted from hydrolysis and polycondensation of glycidoxypropyltrimethoxysilane, dimethyldimethoxysilane and methyltrimethoxysilane. The time to add AgNO3 water solution into the resultant sol was a key factor to synthesize AgTCNQ molecules inside ormosil matrix. AgTCNQ molecules encapsulated in the ormosil showed different photochromic behavior compared with pure AgTCNQ film: normal photochromic reaction can be realized, while reverse photochromic reaction can not. The “cage” model was used to explain this phenomenon.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 9 (1997), S. 239-249 
    ISSN: 1573-4846
    Keywords: sol-gel ; alumina-gel ; multicomponent ; mullite ; phase transformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The capacity of the sol-gel process of producing highly pure, homogeneous alumina-silica based materials had been demonstrated in the last few years. However, a full understanding on the mechanisms associated to sol formation and sol to gel transition has not yet been achieved and is required for the development of a new generation of nano-structurally tailored materials that will significantly enhance the technological importance of the sol-gel process. In this work, tetraethyl orthosilicate (TEOS) and aluminum isopropoxide were used to prepare materials within the entire silica-alumina system. Process parameters, such as gelation time, were correlated to variables of the initial stage of the process, such as pH, temperature of hydrolysis and water/alkoxide ratio. The obtained gels were dried at 105°C and subsequently heat treated at 500 and 1100°C for 3 hours. X-ray diffraction and infrared spectroscopy were used to characterize the materials and phase transformations. Structural information obtained from phase characterization and phase transformations was correlated to the effects of the process variables on sol formation and gelation, providing insights related to the mechanisms involved. The influence of temperature of aluminum isopropoxide hydrolysis on peptization and gelation of the mixtures was noted. The different behavior of mixtures hydrolyzed at low and high temperatures was suggested to be caused by different mechanisms of surface charge formation on the structurally different aluminum hydroxides. Monophasic and diphasic mullite xerogels were produced by changing temperature of aluminum isopropoxide hydrolysis, and led to formation of mullite and Al−Si spinel phases respectively, when treated at 1100°C.
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