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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 10 (1964), S. 617-620 
    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: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 10 (1964), S. 586-589 
    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: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 34 (1988), S. 524-525 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 37 (1991), S. 1613-1624 
    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 family of alkyl-substituted polycyclic aromatic hydrocarbons was pyrolyzed in microbatch reactors at temperatures between 350°C and 425°C. A general pyrolysis network was deduced for these compounds, and it comprised two major and one minor parallel pathways. The first major pathway resulted in products analogous to the major products observed from alkylbenzene pyrolysis. The second major pathway led to products via the cleavage of the strong aryl-alkyl C—C bond. The third pathway led to small amounts of products, presumably through cyclization and condensation reactions. The relative importance of the two major pathways varied for the different compounds. The rates of aryl-alkyl bond cleavage differed for the different compounds, and these rates were quantitatively related to the compounds' localization energies through Dewar reactivity numbers.
    Additional Material: 12 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 39 (1993), S. 1355-1362 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: 1-, 2- and 9-methylanthracene were pyrolyzed neat at temperatures between 350 and 450°C for batch holding times up to 300 min. The pyrolysis proceeded through three parallel primary reaction pathways: one led to anthracene via demethylation; the second to dimethylanthracenes through methyl addition; and the third to methyl-9,10-dihydroanthracenes through hydrogenation. The relative importance of these three paths varied for different methylanthracene isomers. The presence of these primary pathways can be rationalized in terms of recently elucidated hydrogentransfer mechanisms and other aspects of the developing free-radical chemistry of polycyclic alkylarenes. The demethylation rate at 400°C for the methylanthracenes and seven other methylarenes was correlated with Dewar reactivity numbers, which provide a measure of the localization energy, as ln rate (arene yield/min) = 3.7- 7.1 Nts, where Nts is the Dewar reactivity number for the perpheral aromatic carbon atom bearing the methyl substituent. This correlation may be useful in molecular-based reaction models for the conversion of heavy hydrocarbon resources such as coals and heavy oils.
    Additional Material: 6 Ill.
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  • 6
    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: A series of flexible urethane foams was formulated from diisocyanate-terminated polyether prepolymers, using both a polyether diol and an ethylenediamine tetraglycol as extenders. The long-term compression set characteristics and the compression deflection properties of these foams were studied. The swelling effect in a solvent, the free isocyanate content, and the role of a carbon black filler on the flexible urethane foam formulation were also evaluated. It was concluded that the total amount of diisocyanate used in the formulation, rather than a variation in the type of isocyanate, has the greatest influence on molecular structure.
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 43 (1994), S. 122-130 
    ISSN: 0006-3592
    Keywords: interesterification ; lipase ; mass transfer ; solvent-free systems ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The use of solvent-free systems in the oil and fats industry is commonplace. Initial studies on interesterification were carried out in solvent systems because the lipase was immobilized solely by adsorption onto particles of diatomaceous earth. In this study, the mass transfer characteristics associated with the continuous interesterification of olive oil in a solvent-free system have been examined, for lipase immobilized on the three ion-exchange materials: Duolite ES562, Duolite ES568, and Spheroil DEA. The process of immobilization is influenced by the internal structure of the material and this in turn influences the interesterification activity of the catalyst. Individually prepared catalysts for the three support materials have shown that external mass transfer limitations are unlikely even at low flowrates.In the case of Spherosil DEA, with a mean pore diameter of 1480 Å, the wide pores would be expected to reduce internal mass transfer limitations; however, it is more likely that the reduction in activity with increased catalyst loading is due to the lipase molecules being immobilized in a tightly packed monolayer. In such a situation, some active sites of the lipase molecules would become inaccessible to substrate molecules leading to an observed reduction in activity. For Duolite ES568, the observed results are very similar to those seen for Spherosil DEA, however, the pore structure of this support material indicate that some internal mass transfer limitations may also be occurring. Yet the contribution of the individual effects cannot be determined. The results observed for the support Duolite ES562 are different than those observed for the other materials and reflect the heterogeneity of Duolite ES562. The large proportion of narrow pores in the support mean that, for the catalysts examined, immobilization is most likely to have occurred in the external pores of the particles, and as such no internal mass transfer limitation is observed.It is clear that for interesterification the material chosen for enzyme immobilization will have an important role in determining the catalyst efficiency. External mass transfer limitations are very minor and observed internal mass transfer limitations may be caused by both internal mass transfer and the manner in which the immobilization process occurs. © 1994 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 1749-1770 
    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: The amount of residual n-pentane in expandable polystyrene bead foam (PSBF) has an effect on the strength and dimensional stability of the foam. Data were needed to determine how fast the residual n-pentane could be removed to enhance the properties of PSBF. An experiment was designed to determine the diffusivity of n-pentane through PSBF at various temperatures. Mathematical models based on the appropriate diffusion differential equations were then used to predict n-pentane concentrations in in cylinders of PSBF. The diffusivity of n-pentane through PSBF was found to have a magnitude of 1×10-8 to 1×10-6 cm2/sec and to vary with temperature, foam density, n-pentane concentration, and foam structure.
    Additional Material: 19 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 897-903 
    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: The absorption spectra of a series of polyamic acids prepared using various reaction conditions were studied using the ultraviolet (UV), visible, and near-infrared (IR) ranges. The near-IR proved most valuable; the amidization and imidization processes could be followed by observing the change of intensities of the 1950-nm combination amine band and a band at 2300 nm assumed to be a function of the amide group.
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 929-939 
    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: Boron trifluoride forms complexes with nitrogen-and oxygen-containing Lewis bases. These acid-base complexes are sometimes added to epoxy resins to accelerate their cure at elevated temperature (120°C-160°C). Several possible processing concerns with the use of boron trifluoride complexes have been investigated. It was shown that each complex can be readily identified by its distinct fluorine-19 NMR spectrum. All of the boron trifluoride complexes are converted to fluoroboric acid under normal epoxy resin cure conditions. The fluoroboric acid is the true catalyst for epoxy resins. Experimental results show that fluoroboric acid does not catalyze the polymerization of an epoxy resin at room temperature. Finally, it was shown that fluoroboric acid is not hydrolyzed to hydrofluoric acid.
    Additional Material: 5 Ill.
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