2013
DOI: 10.1016/j.jnucmat.2012.08.003
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Evaluating zirconium–zirconium hydride interfacial strains by nano-beam electron diffraction

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Cited by 86 publications
(50 citation statements)
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“…This will cause a decrease in peak width (a) and increase in lattice parameter, d δ-{111} (b). The observed changes in associated strain are quite large; 0.015Å corresponds to a strain of ∆d/d 0.5% and a stress of ∼0.76 GPa but similarly large strains have been seen by both Colas [17] and Barrow [27]. It should also be recalled that these values correspond to local strains in the vicinity of nanoscale precipitates and so stresses in excess of macroscopic yield are possible.…”
Section: Evolution In Peak Widthmentioning
confidence: 77%
See 1 more Smart Citation
“…This will cause a decrease in peak width (a) and increase in lattice parameter, d δ-{111} (b). The observed changes in associated strain are quite large; 0.015Å corresponds to a strain of ∆d/d 0.5% and a stress of ∼0.76 GPa but similarly large strains have been seen by both Colas [17] and Barrow [27]. It should also be recalled that these values correspond to local strains in the vicinity of nanoscale precipitates and so stresses in excess of macroscopic yield are possible.…”
Section: Evolution In Peak Widthmentioning
confidence: 77%
“…This, along with the associated reduction in strain, can be rationalised by appealing to the {111} δ-ZrH habit plane, with its normal parallel to the α-Zr c-axis. A larger misfit strain along the [0001] α-Zr when compared to the [1120] α-Zr has been determined by both Carpenter [26] and Barrow [27]. This gives rise to the characteristic lenticular morphology of the zirconium hydride platelets, with the precipitates' short axis parallel to c, minimising the overall strain energy.…”
Section: Evolution In Lattice Peak Positionsmentioning
confidence: 99%
“…Compared to commonly observed hydrogen rich BCT ε-ZrH 2 hydride, in which (nearly) all eight tetrahedral positions are fully (without loss of generality, we refer to it now as ε-ZrH 2 ) occupied by hydrogen, and non-stoichiometric FCC d-Zr hydride, which has the same sites partially and randomly filled, the g-ZrH has an ordered tetragonal unit cell with four hydrogen atoms on the tetrahedral sites of the (110) plane. According to some studies [19,20] the volume expansions caused by phase transformation of a / g and a / d can reach as high as 12.3% and 17.2%, respectively. Hence, the precipitation of hydrides will introduce significant amount of misfit strain on the Zr matrix and reduces its ductility.…”
Section: Introductionmentioning
confidence: 99%
“…We have been able to attribute the subsidiary maxima to the presence of the hydrides in the packet and to rotation of the orientation of the matrix above/below the hydride packet. Since the precipitation of a hydride involves biaxial straining of the Zr matrix at the hydride-matrix interface [35,36] (with interfacial strains of 7.2% along [0001] α and 4.6% along [1120] α being predicted [36]), there is likely to be accompanying plastic deformation of the matrix. Due to constraint of the matrix, a consequence of the associated volume expansion, this deformation may result in local lattice reorientation due to an excess of dislocations resulting in broader matrix diffraction spots.…”
Section: Discussionmentioning
confidence: 99%