ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Call number: M 00.0567
    Type of Medium: Monograph available for loan
    Pages: 222 S.
    ISBN: 3540590129
    Classification:
    C.3.2.
    Language: English
    Location: Upper compact magazine
    Branch Library: GFZ Library
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract The heat capacity of synthetic, stoichiometric wadeite-type K2Si4O9 has been measured by DSC in the 195≤T(K)≤598 range. Near the upper temperature limit of our data, the heat capacity observed by DSC agrees with that reported by Geisinger et al. (1987) based on a vibrational model of their infrared and Raman spectroscopic data. However, with decreasing temperature, the Cp observed by DSC is progressively higher than that predicted from the vibrational model, suggesting that the standard entropy of K2Si4O9 is likely to be larger than 198.9 ± 4.0 J/K · mol computed from the spectroscopic data. A fit to the DSC data gave: Cp(T) = 499.13 (±1.87) − 4.35014 · 103(±3.489 · 101) · T −0.5, with T in K and average absolute percent deviation of 0.37%. The room-temperature compressibilities of kalsilite and leucite, hitherto unknown, have been measured as well. The data, fitted to the Murnaghan equation of state, gave K o = 58.6 GPa, K o ′ = 0.1 for kalsilite and K o = 45 GPa, K o ′ = 5.7 for α-leucite. Apart from the above mentioned data on the properties of the individual phases, we have also obtained reaction-reversals on four equilibria in the system K2O-Al2O3-SiO2. The Bayesian method has been used simultaneously to process the properties of 13 phases and 15 reactions between them to derive an internally consistent thermodynamic dataset for the K2O-Al2O3-SiO2 ternary. The enthalpy of formation of K2Si4O9 wadeite is in perfect agreement with its revised calorimetric value, the standard entropy is 232.1 ± 10.4 J/K · mol, ∼15% higher than that implied by vibrational modeling. The phase diagram, generated from our internally consistent thermodynamic dataset, shows that for all probable P-T trajectories in the subduction regime, the stable pressure-induced decomposition of K-feldspar will produce coesite + kalsilite rather than coesite + kyanite + K2Si4O9 (cf. Urakawa et al. 1994).
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0959-8103
    Keywords: blend ; molecular dynamics ; dielectric investigation ; DSC measurements ; glass relaxation process ; local process ; molecular weight ; compatibility ; polystyrene ; tetramethyl polycarbonate ; 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: Dielectric and calorimetric measurements have been carried out for tetramethyl polycarbonate/polystyrene (TMPC/PS) blends with different compositions. The effect of varying the molecular weight of the weakly polar component (PS) on the molecular dynamics of the polar segments of TMPC has been thoroughly studied over wide ranges of frequency (10-2-105 Hz), temperature (50-220°C) and number average molecular weight, M̄n, (6500-560 000 g mol-1). All blends were found to be compatible regardless of the composition ratio and the molecular weight of PS. Some new and interesting experimental findings have been observed concerning the effect of molecular weight on the glass temperature and on the broadness of the glass transition and relaxation. Neither the kinetics nor the distribution of relaxation times of the local process observed in pure TMPC was affected by blending with PS, regardless of the composition ratio or the molecular weight of PS. It has been concluded that the mixing of the polymeric components to form a homogeneous single phase (compatible blend) does not take place on a segmental level but on a structural one. The size of this structural level has been suggested to have the same volume as the cooperative dipoles, which is assumed to be the minimum volume responsible for a uniform glass transition (10-15 nm). The molecular weight dependence of the relaxation characteristics of the glass process and temperature could be attributed to the variation in the size and packing of the structural units.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 6 (1981), S. 41-46 
    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 The specific heat capacity of a series of n-alkanes was measured in a powercompensated differential scanning Calorimeter with high resolution. Above the melting point the specific heat capacity increases strictly linear with temperature until 430 K. In this region no transition of first, second or third order could be found. Between 450 and 480 K the nalkanes show an exothermic effect bound to the first run with hermetically sealed sample pans. It is assumed that this effect is a pressure induced epitactic ordering phenomenon correlative to the surface of the sample pan.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 85 (1973), S. 822-823 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 196 (1995), S. 3797-3811 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization behaviour of the series of hydrogenated poly(butadiene-alt-ethene) to poly[butadiene-alt-(1-hexadecene)] copolymers was investigated with the aid of differential scanning calorimetry (DSC) and X-ray measurements. Hydrogenated poly(butadiene-alt-ethene) corresponds to polyethylene and crystallizes in the same way. Hydrogenated copolymers poly(butadiene-alt-propene) through poly[butadiene-alt-(1-decene)] are completely amorphous. In these cases the large branching degree prevents crystallization of the main chains, whereas the side chains are too short to be able to crystallize above the glass transition temperature. The critical length is obviously reached in case of hydrogenated poly[butadiene-alt-(1-dodecene)]. The part of the series with large side chains (hydrogenated poly[butadiene-alt-(1-dodecene)] through poly[butadiene-alt-(1-hexadecene)], shows the most interesting effects, especially hydrogenated poly[butadiene-alt-(1-dodecene)], which shows crystallization depending on thermal history. In these substances the side chains are long enough to cause side-chain crystallization, which becomes more pronounced with increasing length of the side chains. The crystal structure is not excactly to be determined, but some data indicate a model, in which the side chains are packed in a manner as in unbranched alkanes, but are also possible orthorhombic. However, the quality of the crystals formed is not very good, so these regions are better described as ordered domains rather than as crystallites.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 197 (1996), S. 1691-1712 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly[(butadiene-alt-ethene)-co-(butadiene-alt-1-olefin)] terpolymers were synthesized by Ziegler-Natta polymerization using VO(O-neopentyl)2Cl/Al(i-Bu)3 catalyst system in toluene. Variation of the 1-olefin/ethene ratio in the monomer feed produces terpolymers with mixed units of butadiene-alt-ethene and butadiene-alt-1-olefin. After hydrogenation one obtains model substances for LLDPE with a special distribution of methylene sequences between branching points. Differential scanning calorimetry (DSC) was used to determine the degree of crystallinity and the melting behavior. From the melting temperature region, the thickness distribution of the crystal lamellac, and thus the average number of C-atoms between the alkyl branches, can be determined. From detailed X-ray diffractometry, the mean crystallite size, the lattice distortions and the degree of crystallinity was determined for those products which show distinct reflections. The crystallization behavior can only be described by a three-phase model.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 12 (1973), S. 772-773 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Publication Date: 2005-03-01
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Publication Date: 2020-06-22
    Electronic ISSN: 1932-6203
    Topics: Medicine , Natural Sciences in General
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...