Der Einfluss der thermischen Behandlung auf den Binderkoks von Coat- Mix- Material mit Sic- Füller für unterschiedliche Rezepturen und Herstellungsbedingungen
Der Einfluss der thermischen Behandlung auf den Binderkoks von Coat- Mix- Material mit Sic- Füller für unterschiedliche Rezepturen und Herstellungsbedingungen
The effects of the composition and production parameters on porosity, texture and structure of Coat- Mix(CM) materials have been investigated. In particular, CM binder coke was compared with pure binder coke and a conventionally produced material. As filler material which is incompressible, chemical...
Saved in:
Personal Name(s): | Mingam, C. (Corresponding author) |
---|---|
Luhleich, H. / Nickel, Hubertus | |
Contributing Institute: |
Publikationen vor 2000; PRE-2000; Retrocat |
Imprint: |
Jülich
Kernforschungsanlage Jülich GmbH, Zentralbiliothek, Verlag
1989
|
Physical Description: |
94 p. |
Document Type: |
Report Book |
Research Program: |
ohne Topic |
Series Title: |
Berichte der Kernforschungsanlage Jülich
2302 |
Link: |
OpenAccess |
Publikationsportal JuSER |
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245 | |a Der Einfluss der thermischen Behandlung auf den Binderkoks von Coat- Mix- Material mit Sic- Füller für unterschiedliche Rezepturen und Herstellungsbedingungen | ||
260 | |a Jülich |c 1989 |b Kernforschungsanlage Jülich GmbH, Zentralbiliothek, Verlag | ||
300 | |a 94 p. | ||
490 | 0 | |a Berichte der Kernforschungsanlage Jülich |v 2302 | |
520 | |a The effects of the composition and production parameters on porosity, texture and structure of Coat- Mix(CM) materials have been investigated. In particular, CM binder coke was compared with pure binder coke and a conventionally produced material. As filler material which is incompressible, chemically inert and porosity-free, two silicon carbide powders of different grain size were used. The heat treatment of specimens was carried out in stages at temperatures between 400 and 1700°C. The porosity and texture formed during heat treatment by release of gases and shrinkage were characterized using a number of different methods. The volume of open macro- and mesopores was measured using mercury porosimetry and by determination of the real density and air permeability. Meso- and micropore volumes were also measured using helium pycnometer and small angle X-ray scattering. Textures were investigated using scanning and transmission electron microscopy and X-ray diffraction measurements. The cyclic temperature resistance of the specimens produced in the course of this study was examinated by exposure in a high energy electron beam. The surfaces of exposed specimens were examined by optical micro-scopy, scanning electron microscopy, Auger spectroscopy and EDAX. The damage was correlated with the material parameters. The CM material exhibited a significantly better resistance to the high energy electron beam exposure than other ceramic materials tested to date. | ||
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