Library

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
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 87 (1987), S. 5040-5041 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Specific heat measuremnts on high transition temperature perovskite superconductor were conducted from 5.3 K to 345 K. The sample was prepared by mixing stoichiometric amounts of Yttrium oxide, BaO, and CuO so as to yield a 1:2:3 ratio of metals. T he decrease in specific heat at the transition temperature - 91 K is discussed.(AIP)
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 82 (1985), S. 2529-2534 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The proton NMR line shapes of the anhydrous alkali metal hydroxides at 27 and 200 MHz are presented. The structure in the proton resonances of NaOH, KOH, and RbOH is explained using a four-spin planar zig–zag chain model calculation. Second moment calculations show that the observed line shapes are consistent with known crystal structures. The crystal structures of KOH and RbOH, as determined by x-ray powder diffraction, are confirmed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 41 (1985), S. 1139-1141 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 34 (1978), S. 1959-1961 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 1271-1286 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Random copolymers of ethylene with 1-butene, 1-octene, and 1-octadecene have been prepared using a homogeneous vanadium-based catalyst system. Comonomer contents determined by 13C-NMR analysis of polymer solutions are in the range 1-10 mol%. Crystallinities were estimated by means of density measurements, x-ray diffraction, differential scanning calorimetry, laser Raman spectroscopy, and CPMAS 13C-NMR spectroscopy. The results are compared with those obtained for heterogeneous copolymers of ethylene containing 1-4 mol% 1-butene. As the comonomer content is increased, the crystallinity decreases. The dimension perpendicular to the 110 plane in orthorhombic crystallites decreases linearly with crystallinity. This decrease in crystallite size is accompanied by an increase in the size of the orthorhombic unit cell. For copolymers containing large amounts of 1-octene and 1-octadecene, a second crystalline form appears. Differences in estimates of crystallinity are discussed in terms of looser packing in highly branched copolymers and the extent to which the second crystalline form participates in the phase structure.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 175-183 
    ISSN: 0887-6266
    Keywords: polyethylene, linear and branched, X-ray diffraction and 13 C-NMR characterization of ; x-ray diffraction of linear and branched polyethylenes ; nuclear magnetic resonance (NMR) study of linear and branched polyethlenes ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: X-ray diffraction patterns of linear and branched polyethylenes typically show two sharp reflections and an amorphous halo. The position of the halo depends on branch content and temperature. A single curve describes the position of the halo maximum (2θhalo) for a range of liquid hydrocarbons and polyethylenes in the 20-140°C range. At temperatures well below their melting point, branched polymers give 2θhalo values which differ significantly from those observed for the liquid Linear polymers show a greater divergence, indicating that some of the material giving rise to the halo is much better packed than in the liquid.Parallel 13 C NMR spin-lattice relaxation studies suggest that this relatively ordered material has a trans conformation but a low average T1c value. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2447-2458 
    ISSN: 0887-6266
    Keywords: side-chain crystallization ; ethylene copolymers ; 13C NMR ; x-ray diffraction ; solid state NMR ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phase structure of random copolymers of ethylene and ethylene-d4 with 1-octadecene and other 1-alkenes has been investigated. CPMAS 13C NMR spectra show that a fraction of the central sections of C16H33 side chains in ethylene-d4 copolymers are in ordered environments at 298 K. They give rise to resonances from 32.9 ppm to 33.8 ppm, which show that they are in trans conformations; T1C values for this group of resonances range from 1 s to 7 s. The remaining side chains are in an amorphous environment, the internal methylenes having a chemical shift of 30.8 ppm and a T1C close to 0.4 s. A Raman band at 1062 cm-1 in the spectrum of an ethylene-d4-1-octadecene copolymer is consistent with partial crystallization of side chains. Some side-chain crystallization also occurs in a 1-tetradecene copolymer. X-ray diffraction studies suggest that smaller side chains do not crystallize to a significant extent at 298 K. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...