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  • 1980-1984  (14)
  • 1965-1969  (3)
  • 1983  (14)
  • 1968  (3)
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  • 1980-1984  (14)
  • 1965-1969  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 10 (1983), S. 458-463 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary From theoretical considerations it is concluded that the demixing temperatures of moderately concentrated polymer solutions should manifest themselves in a change of the slope of the corresponding DSC trace; the effects are expected to suffice for detection by means of the commercially available dual furnace instrument DSC-2C from Perkin-Elmer. Measurements with 17 mg samples (10 wt.% poly(decyl methacrylate) in iso-octane, lower critical solution temperature) and with 40 mg samples (10 wt.% polystyrene in tert. butyl acetate, upper and lower critical solution temperature) corroborate the above considerations. Since the effects are rather small, special care must be taken to exclude artifacts.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solutions of poly (decyl methacrylate) in isooctane (2,2, 4-trimethylpentane) show lower critical solution temperatures (LCST) that lie well below the thermal degradation of the polymer. The corresponding exothermal theta-temperature (from the Shultz-Flory plot) amounts to 210°C. The increase in solvent quality by pressure turns out to be very pronounced (d Tc/dp ≈ +1 K/bar). With solutions of the polymer in motor oils, high temperature demixing is unlikely to occur below their boiling point. The theoretical evaluation of published experimental data for 11 different systems exhibiting LCSTs demonstrates the following: Under the equilibrium vapour pressure of the solution high temperature demixing is generally observed withing the temperature interval between Tb, the boiling point of the pure solvent (1 bar), and 1,5 Tb. As Tc - Tb increases, the heats of mixing and the pressure influence on Tc increase, too.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 184 (1983), S. 2539-2551 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscosity of solutions of poly(decyl methacrylate)s, PDMA, in 1-pentanol (thermodynamically poor solvent) and in toluence or isooctane (good solvents) was measured up to shear rates of 3 · 104s-1 by means of rotational viscosimeters. The observed pronounced shear thinning is for all solutions well described by the theory of Graessley, with the extension, introduced by Ito. Two parameters, resulting from the evaluation of the flow curves on the basis of the above theory, are discussed: τ0, a characteristic relaxation time of the polymer chain, is found to be in the range of ms. ηfric, a frictional parameter, independent of shear rate, amounts upto 50% of the zero-shear viscosity for the measured solutions. Both, τ0 and ηfric, increase with decreasing solvent quality, increasing molecular weight, and increasing concentration, in accord with theory. A comparatively sharp downward bend, separating two power-law regimes, shows up with moderately concentrated solutions, as the shear rate exceeds about 103 to 104 s-1. This transition is tentatively interpreted as an orientation of the long side chains of PDMA.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 973-974 
    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
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 117 (1968), S. 163-170 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Cloud-point curves for solutions of polymer mixtures containing equal amounts of polystyrene with a “most probable” molecular weight distribution (Pn = 3100) and of polystyrene with a relatively narrow molecular weight distribution (Pn = 800) have been compared with the cloud-point curves of the components. The solvents were cyclohexane and a 3:1 mixture by volume of benzene and methanol. In the mixed solvent a steady increase of the precipitation temperature with polymer concentration is observed throughout the experimentally accessible concentration range; in this case the cloud-point curves extend over a much broader temperature intervall than in cyclohexane as the solvent.In both, single and mixed solvent, the precipitation temperatures of the polymer mixtures for given total polymer concentration lie between those for the components of the same concentration; it becomes evident however from a comparison of the precipitation temperatures at the corresponding partial concentrations that in the case of cyclohexane the long-chain homologs are held in solution by the short ones and vice versa, while in the mixed solvent any addition of polymer reduces the solubility irrespectively of its chain length.
    Notes: Die Trübungskurven für Lösungen von Mischungen aus gleichen Gewichtsanteilen einer Polystyrolprobe mit „wahrscheinlichster“ Molekulargewichtsverteilung (Pn = 3100) und eines Polystyrols mit relativ enger Molekulargewichtsverteilung (Pn = 800) in einem einfachen Lösungsmittel (Cyclohexan) und einem. Mischlösungsmittel (Benzol/Methanol im Vol.-Verhältnis 3:1) wurden mit den Trübungskurven der Komponenten verglichen. Im Mischlösungsmittel nimmt im gesamten experimentell zugänglichen Konzentrationsbereich die Trübungstemperatur mit der Konzentration monoton zu; die Trübungskurve erstreckt sich hier über ein wesentlich größeres Temperaturgebiet als in Cyclohexan als Lösungsmittel.Sowohl in Cyclohexan als auch im Lösungsmittel/Fällungsmittel-Gemisch liegen die Trübungstemperaturen der Polymermischung bei einer bestimmten Gesamtpolymerkonzentration zwischen den Trübungstemperaturen der Lösungen der Komponenten derselben Konzentration. Durch Vergleich der Trübungskurven bei den entsprechenden Partialkonzentrationen der Polymermischung erkennt man jedoch, daß im Falle von Cyclohexan die langkettigen Homologen von den kurzkettigen in Lösung gehalten werden und umgekehrt, während im Mischlösungsmittel jeder Polymerzusatz unabhängig von seiner Kettenlänge die Löslichkeit herabsetzt.Die beobachteten Unterschiede im Entmischungsverhalten von Polymerlösungen im Ein- bzw. Zweikomponentenlösungsmittel werden auf die bevorzugte Aufnahme der Lösungsmittelkomponente des Mischlösungsmittels ins Knäuelinnere zurückgeführt.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1205-1216 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of the viscosity coefficient η of solutions of polystyrene (Mw = 6.0 × 105 and 1.77 × 106) in trans-decalin (TD, θ solvent) and toluene (TL, good solvent) as function of shear rate (11-104 s-1), concentration (4.24-11.21 wt %), and temperature (10-50°C) are reported. As a new theoretically grounded method for the determination of the zero-shear viscosity η0 it is proposed to plot η as a function of $\left({\eta \dot \gamma} \right)^3$. The intercepts of the straight lines obtained by this procedure give η0 in good agreement with directly measured values.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1217-1226 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The viscosity data of moderately concentrated polystyrene solutions in trans-decalin (TD) (θ solvent, θ temperature 21°C) and toluene (TL) (good solvent) reported in Part I are discussed in terms of Graessley's entanglement theory. Under good solvent conditions, Graessley's master curve provides an excellent fit up to high shear rates, whereas in the vicinity of the θ conditions the data have to be modified by a parameter ηfric introduced by Ito and Shishido. The characteristic time of mechanical response to flow of chains approximately given by the shift factor τ0 is found in good solvents to be on the order of the Rouse relaxation time. In poor solvents, close to demixing, τ0 tends to much higher values, indicating a reduced chain mobility. The influence of temperature on the viscosity decreases with increasing shear. The resulting apparent energy of activation of flow shows very small or even negative values at high shear rates. This behavior can be explained by the modified Graessley theory, however, in a quite natural way.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 497 (1983), S. 65-69 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Structural Investigation of K3NO3Synthesis and crystal growth of K3NO3 is described. At room temperature K3NO3 is cubic (a = 521.4 pm, Pm3m) and crystallizes corresponding to the formula (NO2)OK3 in the perovskite-type of structure (diffractometerdata, R = 5.5%).
    Notes: Es wird die Darstellung und Einkristallzüchtung von K3NO3 beschrieben. Bei Zimmertemperatur ist K3NO3 kubisch (a = 521,4 pm, Pm3m) und besitzt gemäß (NO2)OK3 Perowskitstruktur (Diffraktometerdaten, R = 5,5%).
    Additional Material: 3 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 502 (1983), S. 153-157 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On Low-temperature K3NO3Low-temperature Guinier photographs (+20 ← -140°C) indicate a reversible phase-transition at -42°C. From X-ray powder data a structural model based on ordered NO2- groups has been derived (I4cm, a = 726.9(1), c = 1046.3(2) pm).
    Notes: Tieftemperatur-Guinieraufnahmen (+20 ← -140°C) von K3NO3 zeigen eine reversible Phasentransformation bei -42°C an. Aus den Röntgenpulverdaten wird ein Strukturvorschlag abgeleitet (I4cm, a = 726,9(1), c = 1046,3(2) pm), der geordnete NO2--Anionen aufweist.
    Additional Material: 2 Ill.
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  • 10
    Publication Date: 1983-01-01
    Print ISSN: 0170-0839
    Electronic ISSN: 1436-2449
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Published by Springer
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