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  • Polymer and Materials Science  (804)
  • Chemical Engineering  (140)
  • 550 - Earth sciences
  • 1975-1979  (953)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 25 (1979), S. 885-890 
    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: 6 Ill.
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  • 2
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The “condensed” counterions which characterize high-charge-density polyelectrolyte solutions can be analyzed into two subpopulations: (1) site-bound counterions and (2) atmospherically entrapped counterions. The distinction is achieved experimentally by combining the data from self-diffusion coefficient or electrical mobility measurements, which give the amount of “condensed” ions, and those from nmr, chemical shift measurements, which indicate the amount of site-bound ions. In the case of a solution of chondroitin sulfate with excess Co++ counterions, it can be estimated that 20% of the structural charge of the polyion is neutralized by site-bound, dehydrated, condensed counterions, while a further 30% is neutralized by atmospherically entrapped, hydrated counterions.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 660-667 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 operation of a twin screw extruder processing a powder or granular solid is reviewed. The operating variables of screw speed and barrel temperature profile interact with a number of design parameters -  screw design, die geometry, feed zone geometry and with the material properties, in determining machine performance. The factors that determine output and pressure development are specified in a sequence of block diagrams. The dynamic response of an operating machine to disturbances in the steady state conditions is explained in the light of the established relationships and interpreted in conventional control theory terms. Attention is drawn to the importance of mixing in the chambers formed by the screw channels and of the residence time distribution in determining the quality of the final product.
    Additional Material: 14 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 2147-2155 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The role of the intrinsic viscosity [η] as separation parameter in gel permeation chromatography (GPC) was studied for dextrans (from Leuconostoc mesenteroids B512) dissolved in water with deactivated silicagel (Porasil) as the column-filling material. For that purpose specific viscosities of dextran fractions eluted by GPC were measured as a function of the elution volume v. Provided that the elution volumes are corrected for zonal spreading, they are related to the intrinsic viscosities in an unambiguous way, probably reflecting a unique relationship between degree of branching and molecular weights. This was further investigated by developing an iteration method to prepare two calibration curves γ(v) and g(v), respectively, relating ln[\documentclass{article}\pagestyle{empty}\begin{document}$\left[ {\bar \eta } \right]$\end {document}] and InM (M is the molecular weight) to v. It required that the weight-average molecular weight Mw, the number-average molecular weight Mn, and the average intrinsic viscosity [\documentclass{article}\pagestyle{empty}\begin{document}$\left[ {\bar \eta } \right]$\end {document}] for a number of dextran samples (broad distributions) be previously known. The calibration curves found lead to consistent values of the above-mentioned averages. Moreover, they allow-establishment of the [\documentclass{article}\pagestyle{empty}\begin{document}$\left[ {\bar \eta } \right]$\end {document}]-M relationship over the range 5000 〈 M 〈 500,000.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 17 (1978), S. 2503-2518 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To obtain information on the solvent-solute interactions in the dinucleoside monophosphates pertaining to the dimeric subunits of RNA and DNA, we have computed the accessibility of a water molecule to the oxygen atoms of the subunits following the method of Lee and Richards [J. Mol. Biol. 55, 379-400 (1971)]. The solute molecules (dimeric unit) is represented by a set of interlocking spheres of appropriate van der Waals radii assigned to each atom, a solvent (water) molecule is rolled along the envelope of the van der Waals surface, and the total surface accessible to the solvent molecule - and hence the solvent accessibility of various atoms of the solute molecule for different conformations - are computed. From the calculated atomic accessibilities, solvation maps in the (ω′,ω) space have been constructed, keeping ψ at 60°, 180°, and -60°. The C(3′)-endo sugar system in the case of DNA subunit have been considered. The solvation maps describing the solvatability of single and groups of atoms give significant information on the backbone conformational domains that are preferred for solvent interaction, thus adding knowledge to the relative stability of the various possible conformations. The B-DNA-type conformer exposes three polar atoms - namely, PO1, O(3′), and O(1′) - to external solvent, whereas the A-DNA- and C-DNA-type conformers expose only one polar atom - O(3′) and O(1′), respectively - to the solvent. The O(2′) atom of the furanose ring system in the RNA subunit could give added stability via solvent association or interunit hydrogen bonding with or without a bridging water. The superposition solvation maps describing the accessibility of a group of polar atoms help to interpret a good number of phosphodiester conformations observed in a energetically less favored conformational domains in the tRNAPhe crystal. Another intresting fact that results from this study is the prediction that the trans oriented of ω is the most favorable conformations of random-coil polynucleotides in solution.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 17 (1978), S. 1957-1972 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The karl Fischer reagent method has been used to study the drying of whale skeletal muscle myoglobin. Drying curves for metmyglobin were obtained by mechanical pumping (moderate vacuum) and diffusion pumping (high vacum) at 20, 10, 0, -10, and -20°C. Strongly held water is present in about the same amounts as were previously observed with lysozyme. Nearly all of this strongly held water is still present during the drying of acid denatured metmyoglobin. This suggest that a core structure containing strongly held water is still present at pH 4.0. Comparison of the drying of metmyoglobin, deoxymyoglobin, and oxymyoglobin indicates that the iron-coordinated water of methyoglobin is the second most strongly held water of the molocule.
    Additional Material: 12 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 17 (1978), S. 2143-2158 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In an attempt to better our understanding of the conformational stabilities in RNAs, an intensive theoraticl study has been carried out on one of its dimeric subunits, ApA, using an improved set of atom-atom interaction energy parameters and an improved version of energy-minimization technique. The C(3′)0endo and the C(2′)-endo sugar ApA units were sperately considered and 38 probable conformations have been analyzed in each case. The total potential energy, comprising nonbonded, electrostatic, and torsional contributions, was minimized by varying all seven relevant dihedral angles simumtaneously. The result reveal that 17 conformations in the case of C(3′)-endo sugar ApA and 7 confomations in the case of C(2′)-endo sugar ApA unit, the lowest energy conformation corresponds to a nonhelical structure and the A-RNA and the Watson-Crick-yype conformations lie at energy levels of about 0.5 and 1.0 Kcal/mo., respectively, above the lowest energy found. For ApA with the lops of different types in the backbone and they all differ in energies by about 3.5 Kcal/mol with refrence to the lowest energy founs. It is noted that the order ofmprefrence of the base stacking is observed in the A-RNA and the Watson-Crick type conformers. The ApA unit with C(2′)-endo sugar is forced to assume phosphodiester conformations with large deviations fom the expected staggered conformations compared to the ApA unit with C(3′)-endo sugar. The result obtained for ApA are discussed with refrence to those previously obtained for the dApdA unit. Te theoretical predictions are compared with the experimental data on the tRNAPhe crystal, as well as those on fibrous RNAs and RNa subunitlike crystal structures. This study brings out many important aspects of the conformational stability of ApA which have been missed by studies made by others on this system.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 17 (1978), S. 2373-2384 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Measurements of fluorescence depolarization on fumarase labeled with the dye pyrene-butyryl were used to test for previously reported structural changes in this enzymes. These apparent conformation changes were of interest because they seemed to correlate with variation in catalytic activity provoked by changing temperature or pH, or by the presence of a competitive inhibitor. In the present studies, the bound dye pyrene-butyryl and the enzymes were investigated systematically to ensure that simple interpretation of fluorescence depolarization results would be meaningful. This analysis showed that carefully controlled experimental condition were necessary to eliminate a dye component with a short fluorescence lifetime and that it was essential to allow for small variations of lifetime with temperature. Contrary to the previous report, a constant rotational relaxation time of the magnitude expected for a nearly spherical molecule of fumarase was found. No changes were detectable by fluorescence depolarization in the size or shape of pyrene-butyryl-fumarase under the solution conditions tested that caused variation in enzyme activity.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 17 (1978), S. 2523-2524 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 27 (1976), S. 568-572 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Korrelation zwischen dem elektrochemischen Verhalten von Kupferrohren und rotierenden Kupferzylindern in künstlichem MeerwasserEine Laboratoriumsapparatur zur Simulierung der in einem Wärmeaustauscher ablaufenden Korrosionsvorgänge wurde gebaut und ermöglicht sehr genaue elektrochemische Messungen. Die Ergebnisse dieser Messungen wurden mit den Werten verglichen, die sich bei Verwendung von Meßzellen einfacher geometrischer Formen ergaben. Zwischen den Ergebnissen der elektrochemischen Messungen am rotierenden Zylinder und im Inneren einer rohrförmigen Elektrode (die von Elektrolyten durchflossen wird) wurde eine mathematische Beziehung erhalten, welche die folgenden Schlüsse ermöglicht: 1Die strömungsdynamischen Bedingungen in den beiden untersuchten elektrochemischen Zellen sind in elektrochemischer Hinsicht miteinander vergleichbar, wenn die Dicke der Diffusionsgrenzschicht in beiden Fällen die gleiche ist.2Es ist möglich, Meßzellen einfacher geometrischer Form, wie z. B. einen rotierenden Zylinder, zur Untersuchung der Korrosion in elektrolytdurchflossenen Rohren oder Wärmeaustauschern zu verwenden; dabei ergibt sich auch bei hoher Aggressivität des Mediums (wie im Falle des künstlichen Meerwassers) eine Abhängigkeit von den strömungsdynamischen Bedingungen.
    Notes: The experimental conditions corresponding to those which are ascertained in a heat exchanger have been reconstructed in laboratory, with the possibility of performing very accurate electrochemical measurements. The electrochemical results have been compared with those derived from the use of simple geometric electrochemical cells. A mathematical correlation has been obtained between the electrochemical measurements obtained on a rotating cylinder and on the interior surface of a tube-shaped electrode, through which a solution flows. It has been concluded that: (1)the fluid-dynamic conditions, in the two electro-chemical cells we investigated, are comparable between each other, by an electrochemical point of view, when identical values of thickness of the limiting diffusion layers are obtained in the two cases.(2)it is possible to utilize simple cell geometries, such as the one employing a rotating cylinder, to investigate on the corrosion problems which happen in pipes or heat exchangers, in which an electrolyte flows, (even if its aggressiveness is as high as synthetic sea water is) as a function of fluid-dynamic conditions.
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