Formation of Substructure and Texture in Dual-Phase Steels due to Thermal Treatment

2010 ◽  
Vol 160 ◽  
pp. 147-152
Author(s):  
M. Masimov ◽  
Helmut Klein

Microstructure and texture formation in DP steels obtained by thermal treatment at temperatures of 780 °C i.e. between Ac1 and Ac3 and at 900 °C, i.e. above Ac3 and following different cooling techniques were studied by means of X-ray and electron diffraction techniques. The formation of the different structure constituents as well as substructure parameters such as blocks size and misorientation between them induced by thermal treatment was detailed analyzed. Various methods – conventional X-ray methods, high-energy synchrotron radiation and EBSD measuring – the texture of the bcc phase were applied in order to investigate their influence on the results. Beside texture heredity, a softening of the initial texture components induced by cold rolling and of related anisotropy of steels due to thermal treatment was estimated.

1990 ◽  
Vol 68 (6) ◽  
pp. 2719-2722 ◽  
Author(s):  
A. Matsumuro ◽  
M. Kobayashi ◽  
T. Kikegawa ◽  
M. Senoo

2013 ◽  
Vol 772 ◽  
pp. 193-199 ◽  
Author(s):  
Carsten Ohms ◽  
Rene V. Martins

Bi-metallic piping welds are frequently used in light water nuclear reactors to connect ferritic steel pressure vessel nozzles to austenitic stainless steel primary cooling piping systems. An important aspect for the integrity of such welds is the presence of residual stresses. Measurement of these residual stresses presents a considerable challenge because of the component size and because of the material heterogeneity in the weld regions. The specimen investigated here was a thin slice cut from a full-scale bi-metallic piping weld mock-up. A similar mock-up had previously been investigated by neutron diffraction within a European research project called ADIMEW. However, at that time, due to the wall thickness of the pipe, stress and spatial resolution of the measurements were severely restricted. One aim of the present investigations by high energy synchrotron radiation and neutrons used on this thin slice was to determine whether such measurements would render a valid representation of the axial strains and stresses in the uncut large-scale structure. The advantage of the small specimen was, apart from the easier manipulation, the fact that measurement times facilitated a high density of measurements across large parts of the test piece in a reasonable time. Furthermore, the recording of complete diffraction patterns within the accessible diffraction angle range by synchrotron X-ray diffraction permitted mapping the texture variations. The strain and stress results obtained are presented and compared for the neutron and synchrotron X-ray diffraction measurements. A strong variation of the texture pole orientations is observed in the weld regions which could be attributed to individual weld torch passes. The effect of specimen rocking on the scatter of the diffraction data in the butt weld region is assessed during the neutron diffraction measurements.


1991 ◽  
Vol 35 (B) ◽  
pp. 995-1000
Author(s):  
J.V. Gilfrich ◽  
E.F. Skelton ◽  
S.B. Qadri ◽  
N.E. Moulton ◽  
D.J. Nagel ◽  
...  

AbstractIt has been well established over recent years that synchrotron radiation possesses some unique features as a source of primary x-rays for x-ray fluorescence analysis. Advantage has been taken of the high intensity emanating from the bending magnets of storage rings to develop x-ray microprobes utilizing apertures or focussing optics, or both, to provide a beam spot at the specimen of the order of micrometers. The use of insertion devices wigglers and undulatora, can further increase the available intensity, especially for the high energy photons. Beam Line X-17C at the National Synchrotron Light Source (NSLS) at Brookhaven National Laboratory, accepts the unmodified continuum radiation from a superconducting wiggler in the storage ring. Some initial XRF measurements have been made on this beam line using apertures in the 10 to 100 micrometer range. The fluorescent radiation was measured by an intrinsic Ge detector having an energy resolution of 300 eV at 15 kev, and located at 90° to the incident beam in the plane of the electron orbit. In samples containing many elements, detection limits of a few ppm were achieved with 100 μm beams.


1970 ◽  
Vol 14 ◽  
pp. 214-230 ◽  
Author(s):  
M. Matsuo ◽  
S. Hayami ◽  
S. Nagashima

AbstractThe possibility that primary recrystallization textures are influenced by local inhomogeneities of deformation induced in the regions of grain boundaries has been confirmed by comparing the cold rolling and the annealing textures of polycrystalline pure irons which were different in the grain size prior to cold rolling. Analyses were made for the effects of deformation on crystals, namely storage of lattice strain and orientation spread, with application of X-ray diffraction techniques, in order to elucidate the role of in homogeneities of deformation on recrystallization texture formation. Apparent correspondence was found between the orientation dependence of stored strain energy and the textural change on recrystallization. This is a scribed to oriented nucleation in high energy blocks, in the case of originally large-grain material in which the effects of inhomogeneities of deformation are small. But discrepancies arise on this basis in originally small - grain material in which the effects of inhomogeneities of deformation are thought to be considerable. The discrepancy is inferred to arise as an effect of local inhomogeneities of deformation, from the change in the trend of rotational orientation spreads from, a stable orientation and the extent of development of potential nuclei of recrystallization at high energy blocks in the orientation spreads. The change is considered to give rise to the variation in amount of microstrain distribution, which is expressed in recovery characteristics of lattice strains and in the dependence of microstrains on the column length as analyzed by following the procedure of Warren-Averbach.


2013 ◽  
Vol 15 (22) ◽  
pp. 8629 ◽  
Author(s):  
Davide Ferri ◽  
Mark A. Newton ◽  
Marco Di Michiel ◽  
Songhak Yoon ◽  
Gian Luca Chiarello ◽  
...  

2007 ◽  
Vol 352 ◽  
pp. 65-68 ◽  
Author(s):  
Kiyohito Okamura ◽  
Kentaro Suzuya ◽  
Shinji Kohara ◽  
Hiroshi Ichikawa ◽  
Kenji Suzuki

The atomic scale structure of amorphous Si-C-O ceramics fibers produced from the pyrolysis of a polycarbosilane precursor has been investigated by X-ray diffraction using high-energy synchrotron radiation at SPring-8. First peak in the total correlation function T(r) of the amorphous and the heat-treated fibers is analyzed to consist of two contributions: Si-C (1.89 Å) and Si-O (1.61 Å) bonds. The coordination number of C and/or O around Si is about four. This suggests that the Si-C-O fibers basically have a network structure that consists of two tetrahedral units: SiC4 and SiO4. The local chemical and structural orders vary continuously in the materials from the disordered network structure of SiC4 and SiO4 tetrahedra (mixture of amorphous SiC and SiO2) to nanocrystals of SiC and SiO2, through the ternary Si-C-O solid solution which is believed to have an intermediate structure between the amorphous and crystalline states.


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