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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 16 (1970), S. 359-363 
    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 light intensity distribution in a perfectly mixed photoreactor has been studied experimentally and analytically. Experimental measurements of intensities within the reactor were made with a specially designed light probe. These data were then used to test the validity of a model which treats the ultraviolet lamp as a linear source radiating in all directions. It was found that this model, which seems appropriate and allows reasonable computations, is somewhat in error owing to the neglect of the finite size of the lamp and the existence of reflection and refraction effects within the reactor. An empirical correction function was determined for use with the model which then yields predictions in close agreement with experimental data when the reactor is filled with a light absorbing liquid.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 15 (1969), S. 141-144 
    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: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 22 (1976), S. 701-713 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A predictive kinetic model has been developed for fluid catalytic cracking (FCC). The kinetic scheme involves lumped species consisting of paraffins, naphthenes, aromatic rings, and aromatic substituent groups in light and heavy fuel oil fractions. The kinetic model also incorporates the effect of nitrogen poisoning, aromatic ring adsorption, and time dependent catalyst decay. The rate constants for these lumped species are invariant with respect to charge stock composition. The predictive capabilities of the model have been verified for wide ranges of charge stocks and process conditions.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 181-192 
    ISSN: 0887-6266
    Keywords: ternary solutions ; solvent quality ; polystyrene-dioctyl phthalate ; light scattering ; Boger fluid ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymer solvent interactions in the ternary system high molecular weight polystyrene (HMPS), low molecular weight polystyrene (LMPS), and dioctyl phthalate (DOP) have been characterized by means of intrinsic viscometry (IV), dynamic light scattering (DLS), and static light scattering (SLS). Excluded volume exponents have been extracted from the scaling of intrinsic viscosity and translational diffusivity with polymer molecular weight for a mixed solvent of 13 wt % LMPS/87 wt % DOP. The value of the excluded volume exponent, v = 0.45, indicates that HMPS in the mixed solvent DOP/LMPS has apparently assumed a reduced conformation relative to the theta condition. However, SLS measures of the second virial coefficient (A2) confirm that DOP is a theta solvent at our experimental temperature of 22°C and indicate that the addition of LMPS increases A2. SLS also suggests that neither solvent component is strongly preferentially adsorped into the HMPS coil. Our system then is a mixture of a theta solvent and a good solvent that exhibits poor solvent scaling behavior. We believe this to be the first demonstration of such behavior in a system that does not exhibit appreciable preferential adsorption. We conclude by examining our observations in the context of current descriptions of mixed solvent thermodynamics. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1971), S. 157-169 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of twenty N-alkyl-(1-phenylethyl)-carbamates derived from primary, secondary and tertiary alcohols have been investigated using deuterium labeling and high resolution mass spectrometry. These derivatives are suitable for the determination of the isotopic purity of primary and secondary, but not of tertiary alcohols. Several of the primary and secondary alcohol derivatives yield an ion formally equivalent to the product ion of a McLafferty rearrangement. Deuterium labeling established, however, that the usual site specificity associated with the McLafferty rearrangement process was lacking in these carbamate derivatives. In addition a double hydrogen rearrangement process was observed in the mass spectra of several of the carbamates derived from tertiary alcohols.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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