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@PHDTHESIS{TenevaKosseva:60785,
      author       = {Teneva-Kosseva, Guergana I.},
      othercontributors = {Köhne, Heinrich},
      title        = {{O}xidschichtbildung und {M}aterialprobleme metallischer
                      {W}erkstoffe bei {V}erbrennungsprozessen mit {H}eizöl {EL}},
      address      = {Aachen},
      publisher    = {Publikationsserver der RWTH Aachen University},
      reportid     = {RWTH-CONV-122475},
      pages        = {VIII, 171 S. : Ill., graph. Darst.},
      year         = {2006},
      note         = {Zsfassung in dt. und engl. Sprache; Aachen, Techn.
                      Hochsch., Diss., 2005},
      abstract     = {Scope of the present work was the investigation of the
                      oxide scale formation on metallic high-temperature alloys
                      resulting during reaction with the atmosphere of the
                      combustion of industrial gas oil (IGO). The Ni-Cr-based
                      alloys 601 (2.4851), 602 (2.4633), 603, 693 and 617 (2.4663)
                      were tested at elevated temperatures between 900°C and
                      1050°C in a burner rig equipped with a low-NOx
                      recirculation burner by application as material of the
                      burner flame tube. Further on, the oxide scale on a woven
                      wire cloth made of a Ni-Cr-based alloy was analysed. The
                      wire cloth was used as the hot surface of a radiant burner
                      at temperatures of approximately 685°C for an operation
                      time of 844 h. All alloys investigated in the low-NOx burner
                      rig showed following oxide scale structure: a chromium oxide
                      scale at the alloy surface and aluminium or silicon oxide
                      (on alloy 603) beneath. Particles with a composition similar
                      to that of the bulk alloy were found enclosed in the
                      chromium oxide scale. Frequently these particles were
                      located near the oxide-gas boundary indicating an impending
                      local degradation of the chromium oxide scale. Aluminium
                      oxide grew predominantly along grain boundaries in the depth
                      of the bulk. During the test period of up to 3000 h no
                      aluminium oxide scale was found. For longer investigation
                      times accelerated internal oxidation of aluminium was
                      observed.In contrast to aluminium, silicon formed an albeit
                      noncontinuous scale of silicon oxide directly below the
                      chromium oxide layer. The diffusion of chromium towards the
                      surface was inhibited by the silicon scale, which resulted
                      in a slower kinetic of the chromium oxide growth and
                      consequently a thinner chromium oxide scale. However, as the
                      silicon oxide scale was not protective. Mo-oxides formed in
                      the bulk – Mo being an alloying element of alloy 603 –
                      followed by breakaway oxidation. In case of the aluminium
                      alloyed material the formation of nitrides in the bulk
                      indicated the breakdown of the oxide scale. Failure of the
                      alloys was related to massive inward nitrogen diffusion and
                      the formation of aluminium nitrides in the bulk. Therefore
                      it is assumed that in nitrogen rich atmospheres a high
                      aluminium content is unfavourable due to the strong affinity
                      of aluminium to nitrogen. In general it was observed, that
                      at lower temperatures, as a result of a slower growth
                      kinetic, the nitride formation began later.Short term tests
                      of 50 hours of alloy 602, alloy 603 and alloy 693 showed,
                      that a thicker and more uniform oxide layer formed when the
                      burner was operated with standard quality IGO (1700 mg/kg
                      S), compared with the oxide scale formed in the case of
                      operation with fuel with reduced sulphur content (20 mg/kg
                      S). Ventilation with air after burner shut down had no
                      significant effect on chromium oxide scale thickness.The
                      time dependence of the observed growth of the chromium oxide
                      scale was fitted with a power law. A deviation from the
                      parabolic law has been found indicating an oxide loss due to
                      spallation.Reasonable estimation of life time was achieved
                      by logarithmic plots of the time dependence of the chromium
                      depletion measured by line scans on cross sections of the
                      samples.The metallographic investigation of the hot surface
                      of the radiant burner showed a thin continuous chromium
                      oxide layer. No indication of damage of the scale, a small
                      depth of internal oxidation and the absence of a significant
                      chromium depletion zone were found. Hence, a long life time
                      of the woven wire cloth can be expected.},
      cin          = {500000},
      ddc          = {620},
      cid          = {$I:(DE-82)500000_20140620$},
      typ          = {PUB:(DE-HGF)11},
      urn          = {urn:nbn:de:hbz:82-opus-14156},
      url          = {https://publications.rwth-aachen.de/record/60785},
}