Dam breach has catastrophic consequences for human lives and economy. In previous studies, empirical models are often, to a limited extent, due to the inadequacy of historical dam breach events. Physical models, which focus on simulating human behavior during floods, are not suitable for fast analysis of a large number of dams due to the complexities of many key parameters. Therefore, this paper proposes a method for fast evaluation of potential consequences of dam breach. Eight main indices, i.e., capacity of reservoir (CR), dam height (HD), population at risk (PR), economy at risk (ER), understanding of dam breach (UB), industry type (TI), warning time (TW), and building vulnerability (VB), are selected to establish an evaluation index system. A catastrophe evaluation method is introduced to establish an evaluation model for potential consequences of dam breach based on the indices which are divided into five grades according to the relevant standards and guidelines. Validation of the method by twelve historical dam breach events shows a good accuracy. The method is applied to evaluate potential consequences of dam breach of Jiangang Reservoir in Henan Province, China. It is estimated that loss of life in the worst scenario is between that of Hengjiang Reservoir and that of Shimantan Reservoir dam breach, of which fatalities are 941 and 2717, respectively, showing that risk management measures should be taken to reduce the risk of potential loss of life.@en

This work deals with the thermodynamics of hydride formation in 3-D nanoconfined Mg. Two ensembles of nearly monodisperse Mg nanodots (NDs) with different diameters (60 and 320 nm), were grown by the template nanopatterning method, using ultra-thin alumina membranes (UTAMs) with ordered porosity as evaporation masks. Multilayer NDs consisting of 30 nm Mg, 5 nm Ti and 5 nm Pd were deposited on UTAM-coated glass substrates by molecular beam epitaxy. The lateral surface of the NDs is constituted by native MgO. The morphology of the NDs was characterized by field emission scanning electron microscopy and atomic force microscopy. Hydride formation and decomposition was studied at low temperature (363–393 K) by means of optical hydrogenography. Compared to bulk Mg, the plateau pressure for hydrogen absorption in NDs exhibits an upward shift, which is larger for small NDs. Differently, the desorption plateau pressure is almost the same for the two NDs size and is lower than for bulk Mg. These hydrogen sorption features are discussed in the frame of a model that takes into account both interface energy and elastic strain energy in the constrained nanodots. The onset of plastic deformation, marked by a high pressure hysteresis between hydrogen absorption and desorption isotherms, limits the extent of hydride destabilization that can be achieved by elastic strain engineering.@en

This work deals with the thermodynamics of hydride formation in 3-D nanoconfined Mg. Two ensembles of nearly monodisperse Mg nanodots (NDs) with different diameters (60 and 320 nm), were grown by the template nanopatterning method, using ultra-thin alumina membranes (UTAMs) with ordered porosity as evaporation masks. Multilayer NDs consisting of 30 nm Mg, 5 nm Ti and 5 nm Pd were deposited on UTAM-coated glass substrates by molecular beam epitaxy. The lateral surface of the NDs is constituted by native MgO. The morphology of the NDs was characterized by field emission scanning electron microscopy and atomic force microscopy. Hydride formation and decomposition was studied at low temperature (363–393 K) by means of optical hydrogenography. Compared to bulk Mg, the plateau pressure for hydrogen absorption in NDs exhibits an upward shift, which is larger for small NDs. Differently, the desorption plateau pressure is almost the same for the two NDs size and is lower than for bulk Mg. These hydrogen sorption features are discussed in the frame of a model that takes into account both interface energy and elastic strain energy in the constrained nanodots. The onset of plastic deformation, marked by a high pressure hysteresis between hydrogen absorption and desorption isotherms, limits the extent of hydride destabilization that can be achieved by elastic strain engineering.@en