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排序方式: 共有48条查询结果,搜索用时 14 毫秒
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J.G. Dillard H. Moers H. Klewe-Nebenius G. Kirch G. Pfennig H.J. Ache 《Spectrochimica Acta Part B: Atomic Spectroscopy》1984,39(12):1533-1536
The accurate determination of the kinetic energy of X-ray induced Auger electrons, which is necessary in XPS experiments, e.g. for calculating the Auger parameter, is sometimes hampered by peak interferences or by the high secondary electron background. The latter is of special importance for low kinetic energy electrons like e.g. the U(OPV) and U(OVV) Auger electrons. These problems can be circumvented by using electron induced Auger transitions (AES). However, since XPS and AES use different reference points for the energy scales, both scales have to be matched. This can be done by measuring the kinetic energy of an appropriate Auger transition in XPS and relating this value to the maximum of the second derivative of the same peak in AES. 相似文献
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Metal donor atom core electron binding energies have been measured for seven related polydentate Schifr base complexes of nickel(II) and copper(II). The potential donor atoms of all neutral ligands except one and the free metals were also studied. Rather high metal chemical shifts were observed, but no correlation between metal binding energy and known ligand field strength was noted. Satellite peaks are found in the spectra of all paramagnetic complexes. 相似文献
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Kshitish Patankar David A. Dillard Scott W. Case Michael W. Ellis Yongqiang Li Yeh‐Hung Lai Michael K. Budinski Craig S. Gittleman 《Journal of Polymer Science.Polymer Physics》2010,48(3):333-343
Pinhole formation in proton exchange membranes (PEM) may be caused by a process of flaw formation and crack propagation within membranes exposed to cyclic hygrothermal loading. Fracture mechanics can be used to characterize the propagation process, which is thought to occur in a slow, time‐dependent manner under cyclic loading conditions, and believed to be associated with limited plasticity. The intrinsic fracture energy has been used to characterize the fracture resistance of polymeric material with limited viscoelastic and plastic dissipation, and has been found to be associated with long‐term durability of polymeric materials. Insight into this limiting value of fracture energy may be useful in characterizing the durability of proton exchange membranes, including the formation of pinhole defects. In an effort to collect fracture data with limited plasticity, a knife slit test was adapted to measure fracture energies of PEMs, resulting in fracture energies that were two orders of magnitude smaller than those obtained with other fracture test methods. The presence of a sharp knife blade reduces crack tip plasticity, providing fracture energies that may be more representative of the intrinsic fracture energies of the thin membranes. Three commercial PEMs were tested to evaluate their fracture energies (Gc) at temperatures ranging from 40 to 90 °C and humidity levels varying from dry to 90% relative humidity (RH). Experiments were also conducted with membrane specimens immersed in water at various temperatures. The time temperature moisture superposition principle was applied to generate fracture energy master curves plotted as a function of reduced cutting rate based on the humidity and temperature conditions of the tests. The shift with respect to temperature and humidity suggests that the slitting process is viscoelastic in nature. Also such shifts were found to be consistent with those obtained from constitutive tests such as stress relaxation. The fracture energy is more sensitive to temperature than on humidity. The master curves converge at the lowest reduced cutting rates, suggesting similar intrinsic fracture energies; but diverge at higher reduced cutting rates to significantly different fracture energies. Although the relationship between Gc and ultimate mechanical durability has not been established, the test method may hold promise for investigating and comparing membrane resistance to failure in fuel cell environments. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 333–343, 2010 相似文献
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J. G. Dillard H. Moers H. Klewe-Nebenius G. Kirch G. Pfennig und H. J. Ache 《Fresenius' Journal of Analytical Chemistry》1984,319(6-7):638
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Surface analytical investigations of the adsorption of iodine compounds on uranium containing substrates相似文献
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