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
    Springer
    Applied physics 35 (1984), S. 35-40 
    ISSN: 1432-0630
    Keywords: 81.60 Br ; 79.20 Vr
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract In the present work, results of the interaction of O2 with polycrystalline titanium using AES, and ELS techniques, are presented. Changes in the shapes of Ti(LMV) and Ti(LMM) transitions and in the Ti(LM)O(V)/Ti(LMV) and Ti(LMV) Ti(LMM) amplitude ratios as well as a shift of the 34 eV loss peak [Ti(3p level], are studied as function of the oxygen exposure. At O2 pressures equal or less than 10−6 Pa and exposure up to 2000 L(O2) (weak oxidation), the Ti(LM)O(V)/Ti(LMV) and Ti(LMV)/Ti(LMM) ratios show three clearly distinct regions: (i) up to 20L there is a chemisorbed phase with the Ti(LMV)/Ti(LMM) ratio remaining constant and a fast linear increase in the Ti(LM)O(V)/Ti(LMM) ratio. (ii) At exposures higher than 20L the oxidation begins being characterized by a linear variation of the Ti(LM)O(V)/Ti(LMV) and Ti(LMV)/Ti(LMV) ratios, with positive and negative slopes, respectively. (iii) At 125L there is a change in both slopes but no stable value is achieved, despite the O(KLL)/Ti(LMM) ratio remains constant. Hence, it can be concluded that TiO is the final oxide obtained after that treatment, from features like the shape of the transitions and a maximum shift of 3eV of the Ti(3p) level, complemented with ESD experiments. On the other hand, experiments at pressures higher than 10−4Pa with or without the surfaces at 900K (strong oxidation) indicate that the most likely final oxide is TiO2.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 21 (1983), S. 897-899 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 2057-2065 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New polymer-supported catalysts that contain the redox cyclopentadienyl iron moiety [η5C5H5Feη6C6(CH3)5CH2—]+ were prepared with polyvinylchloride (PVC) as support. The active center is attached as a pendant organometallic moiety in the side groups of the PVC chain. Metallocenic groups and the supported polymers with various Fe content were analyzed by spectroscopic techniques and by polarographic and cyclic voltammetry. The absorption spectra show a similar profile to that of the nonsupported cation, which indicates that the supported polymer contains side groups in the chain with metallocenic structures. The new polymer-supported catalysts were characterized by viscometric measurements and by differential calorimetry (DSC). A linear relationship between intrinsic viscosity/[η] and the Fe content was observed. The glass transition temperature (Tg) values are higher than those of PVC without modification.
    Additional Material: 6 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...