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  • Organic Chemistry  (22)
  • Chemical Engineering  (4)
  • 1980-1984
  • 1955-1959  (20)
  • 1925-1929  (6)
  • 1959  (20)
  • 1926  (6)
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 5 (1959), S. 134-134 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 5 (1959), S. 139-144 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Mass transfer in packed columns has been investigated for a variety of column and packing sizes but at flow rates restricted to fully developed turbulent conditions. The present work was undertaken to investigate mass transfer at flow-rate conditions in the transition and laminar regions.A dual treatment of experimental data required a knowledge of the variation of concentration and velocity with radial position. A tracer-injection technique was employed which consisted in the introduction of a tracer gas into the center of a bulk gas stream and the measurement of the tracer-gas concentration at various radial positions downstream. The velocity distribution for the packed column was determined by means of a five-loop, circular, hot-wire anemometer. The test column was a vertical 4-in, pipe. packed with 1/4-in. spherical, ceramic catalyst-support pellets.Mass transfer diffusivity and Peclet number were determined from two solutions of the differential-diffusion equation applied in previous investigations. An analytical solution in terms of Bessel functions was used to calculate values of average diffusivity and Peclet number and a seminumerical solution in terms of homogeneous linear-difference equations to calculate values of point diffusivity and Peclet number.Variation of diffusivity and Peclet number with radial position is shown, average diffusivity and Peclet number being correlated with Reynolds number. The interaction of molecular and eddy mass transfer mechanisms with decreasing mass velocity is illustrated by defining a molecular and an eddy Peclet number and correlating with Reynolds number. Eddy diffusivity is correlated as a function of local flow conditions.
    Additional Material: 14 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 5 (1959), S. 209-212 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: This paper describes general methods for the treatment of binary data which are both precise and convenient. In particular a new and accurate graphical method of determining partial molal quantities is presented.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 5 (1959), S. 514-523 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The origin of interfacial turbulence, spontaneous agitation of the interface between two unequilibrated liquids, has been explained in terms of classical flow, diffusion, and surface processes. The essence of the explanation is the long-known though much neglected Marangoni effect, wherein movement in an interface is caused by longitudinal variations of interfacial tension. It is proposed that interfacial turbulence is a manifestation of hydrodynamic instability, which is touched off by ever present, small, random fluctuations about the interface.A simplified mathematical model has been analyzed in order to detail the mechanism of the “interfacial engine” which supplies the mechanical energy of interfacial turbulence. In its present form the analysis incorporates several drastic simplifications, though ways of removing some of these have been suggested. The groundwork has been laid for the more elaborate analyses that are needed for a decisive test of the theory.The analysis shows how some systems may be stable with solute transfer in one direction yet unstable with transfer in the opposite direction, a striking result. It also suggests that interfacial turbulence is usually promoted by (1) solute transfer out of the phase of higher viscosity, (2) solute transfer out of the phase in which its diffusivity is lower, (3) large differences in kinematic viscosity and solute diffusivity between the two phases, (4) steep concentration gradients near the interface, (5) interfacial tension highly sensitive to solute concentration, (6) low viscosities and diffusivities in both phases, (7) absence of surface-active agents, and (8) interfaces of large extent.That some of these effects have been observed in the laboratory lends credence to the theory.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 114 (1926), S. 313-336 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wird die Totalsynthese des (-)-15,16-Dimethoxy-1,6-cis-erythrinanols- (3) (XI) beschrieben, welches mit einer aus dem natürlichen aromatischen Erythrina-Alkaloid Erysodin hergestellten Verbindung identisch ist.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 42 (1959), S. 1817-1829 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Isolierung von «Subst. Z» aus Nebennierenextrakten wird beschrieben. Der Stoff erwies sich als identisch mit 4,ω-Dihydroxy-3-methoxy-acetophenon, das zum Vergleich durch Synthese in reiner krist. Form bereitet wurde. Auch die Synthese des stellungsisomeren 3, ω-Dihydroxy-4-methoxy-acetophenons («Subst. Iso-Z») wird beschrieben.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 42 (1959), S. 1862-1870 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Curvularia falcata (TEHON) BOEDIJN reduziert das (9S)-9-Methyl-trans-dekalindion-(l,6) (IV) rasch, sowohl in Stellung 1 als auch in Stellung 6, unter Bildung von Hydroxyketonen V und VI (und Enantiomeres von VI) und von Diol VII. Das (9R)-Enantiomere des Eduktes wird langsamer angegriffen, wobei hauptsächlich das Hydroxyketon IX (und Enantiomeres von IX) und das Diol X entstehen.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 42 (1959), S. 2624-2636 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Curvularia falcata (TEHON) BOEDIJN reduziert das (±)-trans-Dekalon-(2) (I, II) zu zwei diastereomeren Paaren von enantiomeren trans-Dekalolen-(2) (III bis VI), von welchen diejenigen mit (2 S)-Konfiguration überwiegen.
    Additional Material: 3 Ill.
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  • 10
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Das nach früheren Versuchen aus WIELAND-GUMLICH-Aldehyd erhältliche Caracurin-V (Formel II) kann uber eine Dibromverbindung in Nor-dihydro-toxiferin und C-Dihydro-toxiferin übergeführt werden.Auch Nor-C-toxiferin-I, C-Toxiferin-I oder Caracurin-V-dichlormethylat können als Ausgangsstoffe für diese Synthese dienen.
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