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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 46 (1995), S. 343-350 
    ISSN: 0006-3592
    Keywords: reverse micelles ; decanol ; amino acid extraction ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The concentrations of dioctyldimethyl ammonium chloride (DODMAC) and 1-decanol in isooctane needed to form reverse micelles by phase contact have been determined. The behavior of these reverse micelles in the extraction of aspartic acid, glutamic acid, and threonine was studied by analyzing all of the ionic species in the aqueous phase. The amino acid is extracted from the aqueous phase by exchanging with the Cl- counterions of DODMAC in the reverse micelles. The ionic species in the reverse micelles tend toward their undissociated states as the water uptake by the reverse micelles decreases. The effect of 1-decanol on the extraction of the amino acids with two negative charges is due to the change in the water uptake of the reverse micelles. The concentration of DODMAC has no effect on the ion exchange of the amino acid with one negative charge with the Cl- counterions of DODMAC in the reverse micelles. Higher molar ratios of decanol to DODMAC favor the selective separation of amino acids with different charge numbers. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 44 (1993), S. 273-278 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The microfibrils and the microfibrillar network in poly(p-phenylene terephthalamide) (PPTA) fibers formed during the coagulation from a monodomain lyotropic fiber are stabilized by critical point drying and characterized by electron microscopy and small angle X-ray scattering. The diameter of the microfibrils varies from 20 to 49 nm depending on the PPTA concentration in the lyotropic solution used for the spinning. A formation mechanism for the microfibrils and the microfibrillar network is suggested. During the coagulation, the spinodal decomposition (phase separation) is assumed to occur before the crystallization (phase transition), resulting in the formation of the microfibrils. The formation of the microfibrillar network is considered to be related to the misorientation of macromolecules and the density fluctuation in the cross-section of the filament during spinodal decomposition.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 1665-1672 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Effects of a series of thiophenols R—ArSH with substituting groups R in the para-position and 2-mercaptobenzoic acid on the kinetics of polymerization of methyl methacrylate (MMA) photoinitiated by benzoin isopropyl ether (BIPE) were investigated using an autorecording dilatometer. Thiophenols were found to have a dual effect on polymerization: reducing induction time and accelerating rate of polymerization. A mechanism was proposed suggesting that this increased rate of polymerization and reduced induction time with addition of a thiophenol is due to the fact that, instead of consuming radicals, the dissolved oxygen in the MMA/BIPE system can be converted into active radicals through effective photooxidation of the thiophenol. Although the maximum increase in rate of polymerization is of a minor difference between various thiophenol compounds, reduction in induction time is strongly dependent on the nature of substituting groups in the following order: —CH3 〉 —CH(CH3)2 〉 —OCH3 or —Cl 〉 —H. 2-Mercaptobenzoic acid, on the other hand, increases induction time and decreases rate of polymerization. © 1993 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 21 (1990), S. 127-131 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence on silver colloids of the addition of KCI was directly investigated by means of transmission electron microscopy (TEM). It was found that the particle size increased and the surfaces of the crystal particles of the silver became covered with an overlayer. Additionally, the pattern of aggregation was found to be chain-like. These changes were very different from those caused by adding pyridine. The mechanism affecting the colloid and the intensity of the surface-enhanced Raman scattering signals of adsorbed molecules on adding KCl to silver colloid is discussed.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 33 (1995), S. 749-754 
    ISSN: 0749-1581
    Keywords: NMR ; 13C NMR ; 1H NMR ; kaurane diterpenoid ; absolute configuration ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new ent-kaurane diterpenoid glycoside has been shown to be the main sweetening constituent of the traditional medicines Aster tongolensis and A. ageratoides native to China. This study involved the total 1H and 13C spectral assignment of the compound and its degraded product by means of two-dimensional NMR techniques (COSY, NOESY, HETCOR and TOCSY) and resulted in unambiguous spectral assignments, particularly in the heavily convoluted regions of the spectra. Concerning the absolute stereochemistry, the sweetener was determined to be (4R,5S,8S,9S,10,13R)-16,17-dihydroxykauran-19-oic acid β-D-glucopyranosyl ester through a combination of circular dichroism and 2D NMR techniques.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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