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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 27 (1992), S. 5101-5107 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Different crystalline structures of lineartrans-quinacridone were prepared and analysed by combination of X-ray diffraction, specific surface areas, optical and scanning electron microscopy, infrared spectroscopy, spectrophotometric analysis and differential thermal analysis. The lattice parameters of each crystalline phase were determined by X-ray diffraction. A new crystalline phase of this pigment was obtained and named theς-phase. Isothermal crystallization studies indicated that the crystallographic texture induced by pressure has a strong influence on the crystallization behaviour of this dyestuff.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-5087
    Keywords: gibberellins ; structure-activity ; flowering ; growth ; juvenility ; Prunus avium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract When applied to spurs of mature Prunus avium before floral initiation, gibberellins GA1, GA4 and GA3 inhibited floral initiation by 9–17%, GA7 by 43%, GA3 by 65–71% and 2,2-dimethyl GA4 by 78%. GA9 and GA20 were inactive. Thus activity only of the GAs with a C-3 hydroxyl was increased markedly by a double bond in the C-1,2 or C-2,3 position, and activity increased with increasing hydroxylation. None of the GAs affected the total number of buds (vegetative and floral) surviving in the spur. Measured by the threshold dose required for activity, seedling shoot growth responses to GA3, GA7, GA1 or GA4 resembled those of floral initiation, but di-methylation of GA4 at C-2 had no effect, and GA9 was as active as GA7. Mature shoots, including those on rooted cuttings, were less responsive to GA treatment than were juvenile shoots, with terminal shoots on mature trees more responsive than spur shoots. Spur shoot growth on mature trees responded to GA3 and to a lesser extent GA7, but not to GA1 or GA4. However, all these GAs promoted the growth of terminal shoots on mature trees to similar extents, whereas 2,2-dimethyl GA4 was less active than GA4 The differences between juvenile and mature shoot growth in sensitivity to a C-1,2 or C-2,3 double bond, and between mature shoot growth and floral initiation in GA-structure requirements, indicate that phase change alters the GA complement and/or GA receptor/transduction mechanisms of P. avium. The difference in sensitivity to 2,2-dimethyl GA4 indicates that floral initiation and growth have different requirements for GA transport and/or action.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 10 (1989), S. 973-982 
    ISSN: 1572-9567
    Keywords: binary diffusion ; 2,2-dimethylbutane ; 2,3-dimethylbutane ; n-heptane ; n-hexane ; liquid mixtures ; 3-methylpentane ; Taylor dispersion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract This paper presents a study of the influence of branching in the binary diffusion coefficients of n-heptane + n-hexane isomers, in the liquid state. The measurements have been made with the Taylor dispersion technique, at several compositions, at 283 and 298 K, for the X + n-heptane mixtures, where X= n-hexane, 3-methylpentane, 2, 3-dimethylbutane, and 2, 2-dimethylbutane. The results show a very interesting behavior of the composition dependence of the binary diffusion coefficients, presenting a maximum, for compositions about a molar fraction of n-heptane of 0.5, which increases with the increase in the degree of branching, suggesting the possibility of order-disorder effects caused by stereochemically favored packing in the liquid phase and energetically favored segment interaction in the liquid mixtures. An attempt to apply the van der Waals model to these data could not predict the experimental binary diffusion coefficients of these systems within the experimental accuracy.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 14 (1993), S. 1131-1143 
    ISSN: 1572-9567
    Keywords: refrigerants ; R32 ; R125 ; viscosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract This paper reports new measurements of the viscosity of R32 and R125, in both the liquid and the vapor phase, over the temperature range 220 to 343 K near the saturation line. The measurements in both liquid and vapor phases have been carried out with a vibrating-wire viscometer calibrated with respect to standard reference values of viscosity. It is estimated that the uncertainty of the present viscosity data is one of 0.5–1%, being limited partly by the accuracy of the available density data. The experimental data have been represented by polynomial functions of temperature for the purposes of interpolation.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 14 (1993), S. 33-44 
    ISSN: 1572-9567
    Keywords: high pressure ; refrigerants ; R134a ; viscosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The paper reports new measurements of the viscosity of liquid R134a over the temperature range 235 to 343 K and pressures up to 50 MPa. The measurements have been carried out in a vibrating-wire viscometer calibrated with respect to the viscosity of several liquid hydrocarbons. It is estimated that the uncertainty in the viscosity data reported is ±0.6%. The data therefore have a lower uncertainty than that of earlier measurements of the viscosity of this environmentally acceptable regrigerant. The viscosity data have been represented as a function of density by means of a formulation based upon the rigid, hard-sphere theory of dense fluids with a maximum deviation of ±0.3%. This representation allows the present body of experimental data to be extended to regions of thermodynamic state not covered by the measurements.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 20 (1999), S. 365-373 
    ISSN: 1572-9567
    Keywords: R134a ; R32 ; R125 ; refrigerants ; vibrating-wire viscometer ; viscosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract This paper reports the results of the measurement of the viscosity of R134a close to the saturation line in the vapor phase. The new measurements were carried out in a vibrating-wire viscometer specially constructed for the purpose, and the results have an accuracy of ±2%. In addition, the opportunity is taken to present a reevaluation of earlier measurements along the saturation line of the viscosity of R32 and R125. Improved equations of state for these fluids are now available and can be employed to generate improved values for the viscosity.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 13 (1992), S. 773-790 
    ISSN: 1572-9567
    Keywords: n-decane ; n-hexane ; n-octane ; n-pentane ; toluene ; viscosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract This paper reports new measurements of the viscosity of toluene, n-pentane, n-hexane, n-octane, and n-decane at pressures up to 250 MPa in the temperature range 303 to 348 K. The measurements were performed with a vibrating-wire viscometer and with a relative method of evaluation. Calibration of the instrument was carried out with respect to reference values of the viscosity of the same liquids at their saturation vapour pressure. The viscosity measurements have a precision of ±0.1% but the accuracy is limited by that of the calibration data to be ±0.5%. The experimental data have been represented by polynomial functions of pressure for the purposes of interpolation. The data are also used as the most precise test yet applied to a representation of the viscosity of liquids based upon hard-sphere theory.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 14 (1993), S. 1131-1143 
    ISSN: 1572-9567
    Keywords: refrigerants ; R32 ; R125 ; viscosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract This paper reports new measurements of the viscosity of R32 and R125, in both the liquid and the vapor phase, over the temperature range 220 to 343 K near the saturation line. The measurements in both liquid and vapor phases have been carried out with a vibrating-wire viscometer calibrated with respect to standard reference values of viscosity. It is estimated that the uncertainty of the present viscosity data is one of 0.5–1%, being limited partly by the accuracy of the available density data. The experimental data have been represented by polynomial functions of temperature for the purposes of interpolation.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 46 (1992), S. 733-737 
    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: Poly(propylene oxide-b-ethylene oxide) (PPOPEO) surfactant has been used as a surface tension modifier. In this study, the graft copolymer made of poly(methyl methacrylate) (PMMA) main chain and PPOPEO graft chain behavior at water/toluene interface was observed. Interfacial tension measurements were conducted by dissolving the graft copolymer in toluene at a concentration range 1 wt % -0.0003. The results confirmed the surfactant behavior of graft copolymers, which presented a PMMA/PPOPEO ratio dependence. The critical micellar concentration (CMC) was observed. Above the CMC, the graft copolymers tend to form a monomolecular association that depends upon copolymer molecular weight. © 1992 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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