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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Zeitschrift für Lebensmittel-Untersuchung und -Forschung 205 (1997), S. 158-164 
    ISSN: 1431-4630
    Keywords: Key words Adulteration ; Carbon-13 ; Citric acid ; Ethanol ; Malic acid ; Tartaric acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract  The δ13C-values of organic acids and their correlations to those of the sugar and ethanol, respectively, from 57 EU data bank wines of the Rheinpfalz area (years 1991 – 1993) and from some of their corresponding musts have been determined. In addition to the well established difference between fermented sugar and ethanol (Δδ13C = –1.7±0.2‰), a new constant correlation was found in wine for ethanol and citric acid (Δδ13C = +2.4±0.4‰). From this result a fixed δ-value difference for citric acid in wine to the fermented sugar of +0.7±0.6‰ can be deduced. The δ13C-values of L-malic acid and L-tartaric acid in must were not altered by the alcoholic fermentation; they should therefore directly provide access to the δ13C-value of the natural sugar in must. However, in non-adulterated wines the expected δ13C-value differences between these acids and ethanol showed unsatisfactory correlation coefficients. For L-malate this is attributed to the secondary (partial) degradation of this acid by the malolactic fermentation; a corresponding correction is envisaged in order to make L-malate available as an internal standard. As a reason for the unsatisfactory correlation between L-tartaric acid and ethanol, it is supposed that the time of its maximum biosynthesis period does not coincide with that of glucose in the grape ripening period.
    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. 1035-1042 
    ISSN: 1573-4846
    Keywords: sol-gel coating ; silver colloids ; UV-VIS spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Ag colloid-containing coatings on soda lime glass and fused silica are prepared via the sol-gel process. To incorporate Ag+-ions in the coatings homogeneously, they are stabilized by a functionalised silane (aminosilane) and then mixed with the basic sol prepared from 3-glycidoxypropyl trimethoxysilane (GPTS) and tetraethoxysilane (TEOS). Crack-free and transparent coatings with a thickness of 0.5 to 1.2 μm, are obtained by heat treatment between 120°C and 600°C. The Ag-colloid formation was monitored by UV-VIS spectroscopy as a function of temperature. The investigations reveal that the substrate has a deciding influence on the Ag-colloid formation caused by alkali diffusion from the substrate into the coating. High resolution transmission electron microscopy (HRTEM) investigations prove that poly-crystalline AgxOy-nanoparticles are formed during thermal densification in the coatings and that this change is accompanied by a vanishing of the yellow colour of the coatings. A post-heat treatment in a reducing atmosphere (90% N2, 10% H2) turns back the yellow colour and single-crystalline Ag-colloids can be detected by HRTEM. A suitable choice of the temperature and time conditions allows the control of the colloid size during heat treatment in a reducing atmosphere. For comparison, ion-exchange experiments have been carried out which showed that a spontaneous Ag-colloid formation was achieved in the soda lime substrate at 400°C. Since Ag containing SiO2-coatings remained colourless after thermal treatment between 400°C and 600°C in air, on soda lime substrates, a remarkable diffusion of Ag+ into the substrate was excluded.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 8 (1997), S. 1035-1042 
    ISSN: 1573-4846
    Keywords: sol-gel coating ; silver colloids ; UV-VIS spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Ag colloid-containing coatings on soda lime glass and fused silica are prepared via the sol-gel process. To incorporate Ag+-ions in the coatings homogeneously, they are stabilized by a functionalised silane (aminosilane) and then mixed with the basic sol prepared from 3-glycidoxypropyl trimethoxysilane (GPTS) and tetraethoxysilane (TEOS). Crack-free and transparent coatings with a thickness of 0.5 to 1.2 μm, are obtained by heat treatment between 120°C and 600°C. The Ag-colloid formation was monitored by UV-VIS spectroscopy as a function of temperature. The investigations reveal that the substrate has a deciding influence on the Ag-colloid formation caused by alkali diffusion from the substrate into the coating. High resolution transmission electron microscopy (HRTEM) investigations prove that poly-crystalline AgxOy-nanoparticles are formed during thermal densification in the coatings and that this change is accompanied by a vanishing of the yellow colour of the coatings. A post-heat treatment in a reducing atmosphere (90% N2, 10% H2) turns back the yellow colour and single-crystalline Ag-colloids can be detected by HRTEM. A suitable choice of the temperature and time conditions allows the control of the colloid size during heat treatment in a reducing atmosphere. For comparison, ion-exchange experiments have been carried out which showed that a spontaneous Ag-colloid formation was achieved in the soda lime substrate at 400°C. Since Ag containing SiO2-coatings remained colourless after thermal treatment between 400°C and 600°C in air, on soda lime substrates, a remarkable diffusion of Ag+ into the substrate was excluded.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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