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
Filter
Collection
Language
  • 1
    Series available for loan
    Series available for loan
    Reykjavík : Okustofnun
    Associated volumes
    Call number: S 05.0369(2007, 2)
    In: Report
    Type of Medium: Series available for loan
    Pages: iv, 37 S.
    ISBN: 9789979682288
    Series Statement: Report / United Nations University Geothermal Training Programme 2007, 2
    Classification:
    Geothermal Energy
    Location: Lower compact magazine
    Branch Library: GFZ Library
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 92 (1988), S. 2702-2706 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 93 (1989), S. 2610-2614 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 93 (1989), S. 5238-5248 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 94 (1990), S. 6936-6939 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 9427-9439 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The properties of Zn, Au, and Zn–Au films on Ru(001) have been studied using thermal desorption mass spectroscopy (TDS) and core and valence-level photoemission. TDS spectra show desorption of Zn from Ru(001) at 450 (multilayer), 490 (second layer), and 720 K (first layer). The monolayer of Zn desorbs following zero-order kinetics with an activation energy for desorption of 36 kcal/mol. Photoemission studies show that the Zn(3s) and Zn(3d) levels of Zn bonded to Ru are shifted 0.5 eV toward lower binding energy with respect to the corresponding levels of pure metallic Zn. The direction of this binding-energy shift together with the results of CO-TDS indicate that Zn is withdrawing electrons from the Ru(001) surface. Such charge transfer is in part responsible for the large stability of the Ru–Zn bond. Au desorbs from Ru(001) at temperatures of 1175 (multilayer) and 1260 K (first layer). For a monolayer of Au deposited on Ru(001), the positions of the Au(4f ) and Au(5d) levels are very close to those of the surface atoms of Au(111), indicating that charge transfer between Au and Ru is minimal. A comparison of the desorption temperature for a monolayer of Zn or Au from Ru(001) with values previously reported for the desorption of monolayers of alkali (K and Cs), noble (Cu and Ag), and transition (Mn, Ni, and Pd) metals indicates that the strength of a metal–metal bond in a bimetallic surface depends on (1) the bulk cohesive energy of the individual metals (which gives an indication of the tendency of the element to form strong metal–metal bonds), and (2) the charge transfer within the bond. Zn and Au alloy when coadsorbed on Ru(001). Results for submonolayer coverages of Zn and Au show that the Zn–Ru and Zn–Au bonds in the trimetallic system are more stable than the corresponding bonds in Zn/Ru(001) or Zn–Au alloys. This phenomenon is probably caused by synergistic interactions in three center metal–metal bonding. The formation of ZnAu alloys induces a shift of ∼+1.0 eV in the Au(4f ) and Au(5d) levels, and −0.2 eV in the Zn(3s) and Zn(3d) levels. The shift in the core and valence levels of Au is caused by rehybridization of the Au(5d,6s,6p) levels, while the shift in the Zn levels comes from a contraction in volume.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 740-747 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The interaction between B and CO on Ru(0001) has been studied by means of thermal desorption mass spectroscopy, Fourier transform infrared reflection absorption spectroscopy, and x-ray photoelectron spectroscopy. Boron adatoms poison CO chemisorption approximately on a one-to-one basis. No reaction or direct bonding between B and CO was observed. The B⋅⋅⋅CO interaction is repulsive due to the electron-acceptor nature of both adsorbates. Boron adatoms modify the electronic and chemical properties of first and second nearest-neighbor metal atoms. In the presence of B, the CO desorption temperature decreases, whereas the O(1s) binding energy and CO stretching frequency increase. These trends are a consequence of (1) a reduction in 2π* back donation caused by competition for metal electrons between CO and B and (2) repulsive electrostatic interactions between the negative charges on CO and B. The infrared results indicate that metal atoms strongly affected by B are only occupied when no more unperturbed Ru sites are available on the surface, or when the high temperature of the system favors CO migration (due to entropic effects) onto these energetically less favorable sites.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 7814-7825 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Adsorption of CO on ultrathin Cu films supported on Pt(111) has been studied using infrared reflection absorption spectroscopy (IRAS). Our results indicate that the infrared intensities of adsorbed CO are not representative of the relative composition of the Cu〈1.0/Pt(111) surfaces. The Cu-bonded CO molecules screen CO molecules bonded to Pt, making them invisible in the infrared spectrum. The "screening'' effect depends on the morphology and polarizability of the Cu overlayer. Changes in the morphology of the Cu adlayer produce large variations in the position and line shape of the Cu–CO signal in the infrared spectrum. CO molecules bonded to small Cu clusters show a higher (∼40 cm−1) C–O stretch frequency than CO molecules adsorbed on large Cu islands. The present results were compared with those reported in the literature for the CO/Cu/Ru(0001) and CO/Cu/Rh(100) systems. For CO adsorbed on supported monolayers of Cu, a correlation was found between the strength of the Cu–CO bond, the amount of π backdonation, and the C–O stretch frequency. This correlation cannot be explained using simple models of molecular orbital theory. On the bimetallic surfaces, the C–O stretch frequency is more sensitive to the charge on the metal center to which CO is bonded, than to the electron population of the CO(2π) orbitals.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 83 (2000), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The present study examined the effects of dry grinding, using ball-milling, on the structure of reference well-crystallized (KGa-1) and poorly crystallized (KGa-2) kaolinite powders from Georgia. Grinding produced a strong structural alteration, mainly along the c axis, resulting in disorder and total degradation of the crystal structure of the kaolinite and the formation of an amorphous product. The surface area increased with grinding time, mainly in KGa-2 (maximum value 50.27 m2/g), a result associated with particle-size reduction. These particles became more agglomerated with grinding, and the surface area decreased after 30 min, as confirmed by scanning electron microscopy and particle-size-distribution analysis. There was a limit to particle-size reduction with grinding time. When grinding time was increased, the original endothermic differential thermal analysis (DTA) effects of dehydroxylation in both samples shifted to lower temperatures, decreased in intensity, then disappeared completely after 120 min of grinding. The temperature of the characteristic first exothermic effect shifted slightly to lower temperatures with grinding, although the DTA effects did not increase with grinding time in either kaolinite sample, at least up to 325 min. The amorphous, mechanically activated kaolinite converted into low-crystalline mullite nuclei at a lower temperature than did the unground samples, as deduced by thermal and X-ray observations. This effect was especially important for the KGa-2 sample. Grinding did not seem to influence the formation of silicon-aluminum spinel from kaolinite. The present results may explain why ground kaolinite samples prepared via different routes—e.g., with differences in grinding—behave differently during high-temperature transformations, as reported in the related literature.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    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...