Integrity of emergency systems [of power supply]

The reliability of emergency power systems has improved steadily since the earliest installations. The generator set, and its maintenance, will probably always be the most critical part of the system, but the application of the set and the rest of the system often prevents it from supplying power. This paper concentrates on the integrity of the system. Section II illustrates some actual cases of early failure of the wiring and environmental damage to the generator set. Section III addresses some misunderstandings of generator set applications and Section IV reviews progress with strengthening code requirements     

Real-time in situ study of hydrogen diffusion in amorphous Si formed by ion implantation

The diffusion of hydrogen in amorphous silicon formed by ion implantation is studied using real-time elastic recoil detection analysis. An activation energy for H diffusion of 1.82 eV is determined in a single ramped anneal. This activation energy is consistent with diffusion studies in the high H concentration regime. The low beam current employed is found to have a negligible influence on the H diffusion within the sensitivity of the measurement. Further refinements for increased accuracy of this technique are discussed.     

Nuclear Data Sheets for A = 211

The evaluated spectroscopic data are presented for 11 known nuclides of mass 211 (Hg, Tl, Pb, Bi, Po, At, Rn, Fr, Ra, Ac, Th). The ²¹¹Pa nuclide is included here but its identification remains uncertain. For ²¹¹Hg, ²¹¹Tl, ²¹¹Ac and ²¹¹Th nuclei, only the ground–state information is available. Their decay characteristics are mostly unknown. ²¹¹Fr is suggested to decay partially through ε decay mode, but its decay scheme remains poorly known. While high–spin excitations, including several isomers, are well studied in ²¹¹Pb, ²¹¹Bi, ²¹¹Po, ²¹¹At, ²¹¹Rn and ²¹¹Fr, the particle–transfer data are available for only ²¹¹Po and ²¹¹Bi.This evaluation was carried out as part of joint IAEA–ICTP workshop for Nuclear Structure and Decay Data, organized and hosted by the IAEA, Vienna and ICTP, Trieste, August 6–17, 2012. This work supersedes previous A=211 evaluation (2004Br45) published by E. Browne which covered literature before January 2003.     

The quasi-static compression of non-circular prismatic blocks between very rough platens using the “friction hill” concept

There exists a similarity between the two-dimensional pressure distribution (“friction hill”) over the ends of a non-circular prismatic block when plastically compressed between very rough dies and the torsion stress function made manifest by the sand heap analogy which is used for the complete plastic torsion of non-circular prismatic bars.

This sand heap analogy is applied to provide an overestimate of the load required for the quasi-static compression of a rectangular block between very rough platens and to give an insight into the deformation pattern.

Annealed tellurium lead specimens of different shapes compressed between very rough platens illustrate the approach to other non-circular sections.     

Low-endurance fatigue of an aluminium alloy and a stainless steel in plane bending at ambient and elevated temperatures

Flat uniform specimens were cyclically bent over formers. At room temperature two strain ratios were used, R = −1 and 0, i.e. reversed symmetrical and asymmetrical strains, respectively, the strain ratio being defined as the ratio of the minimum to the maximum strain in a cycle. The increase in the value of the strain ratio was found to decrease the fatigue life of the aluminium alloy and to increase it for the stainless steel. For room temperature tests and at R = −1, the bending moment at maximum strain was found to increase in the early part of the test and was then followed by a decrease until fracture occurred, whilst for R = 0 a continuous decrease occurred throughout the tests. The effect of test temperature on fatigue life was found to be considerable and throughout the tests at elevated temperature the cyclic bending moment decreased.     

Direct ultraviolet spectrophotometric determination of total sulfide and iodide in natural waters

A technique is described that allows the determination of total dissolved sulfide in natural waters using direct ultraviolet detection of the HS- ion. The concentration of bisulfide is determined by measuring absorption from 214 to 300 nm and then deconvolution of the HS- spectra from the complex spectrum of natural fluids. A nonlinear least-squares fitting approach is used for the deconvolution. At a pH near 8, where >95% of total sulfide is present as HS-, the results are indistinguishable from total sulfide measured using the methylene blue method in a wide range of sample types and matrixes including freshwater from groundwater wells, marine hydrothermal vent fluids, and marine sediment porewaters. The method allows simultaneous determination of other UV-absorbing ions, including nitrate, bromide, and iodide, in samples with low total sulfide concentrations. Bisulfide concentrations can be determined in samples with low background absorption, such as well water and hydrothermal fluids, with a detection limit of < 1 microM. The detection limit for bisulfide in sediment porewaters that have a high organic loading, which produces background absorbances of approximately 0.5 A at 260 nm in a 1-cm cuvette, is 5 microM. The only chemical manipulation required is buffering acidic samples to pH > 7 and filtration of particulate-rich samples.     

pH Sensing Properties of Flexible,Bias‐Free Graphene Microelectrodes in Complex Fluids: From Phosphate Buffer Solution to Human Serum

Advances in techniques for monitoring pH in complex fluids can have a significant impact on analytical and biomedical applications. This study develops flexible graphene microelectrodes (GEs) for rapid (<5 s), very‐low‐power (femtowatt) detection of the pH of complex biofluids by measuring real‐time Faradaic charge transfer between the GE and a solution at zero electrical bias. For an idealized sample of phosphate buffer solution (PBS), the Faradaic current is varied monotonically and systematically with the pH, with a resolution of ≈0.2 pH unit. The current–pH dependence is well described by a hybrid analytical–computational model, where the electric double layer derives from an intrinsic, pH‐independent (positive) charge associated with the graphene–water interface and ionizable (negative) charged groups. For ferritin solution, the relative Faradaic current, defined as the difference between the measured current response and a baseline response due to PBS, shows a strong signal associated with ferritin disassembly and the release of ferric ions at pH ≈2.0. For samples of human serum, the Faradaic current shows a reproducible rapid (<20 s) response to pH. By combining the Faradaic current and real‐time current variation, the methodology is potentially suitable for use to detect tumor‐induced changes in extracellular pH.     

The Columbia University sub-micron charged particle beam

A lens system consisting of two electrostatic quadrupole triplets has been designed and constructed at the Radiological Research Accelerator Facility (RARAF) of Columbia University. The lens system has been used to focus 6 MeV ⁴He ions to a beam spot in air with a diameter of 0.8 μm. The quadrupole electrodes can withstand voltages high enough to focus ⁴He ions up to 10 MeV and protons up to 5 MeV. The quadrupole triplet design is novel in that alignment is made through precise construction and the relative strengths of the quadrupoles are accomplished by the lengths of the elements, so that the magnitudes of the voltages required for focusing are nearly identical. The insulating sections between electrodes have had ion implantation to improve the voltage stability of the lens. The lens design employs Russian symmetry for the quadrupole elements.     

Oxidation of Starch by Hydrogen Peroxide in the Presence of UV Light-Part II

Various reaction variables in the hydrogen peroxide oxidation of starch in the presence of UV light have been investigated. Higher carboxyl and carbonyl contents of oxystarches were obtained under acidic than under alkaline conditions. Extent of oxidation was found to increase with time. Increasing the concentration of hydrogen peroxide results in an increase in the carboxyl and carbonyl contents. Apparently, air has no effect on the degree of oxidation whereas, oxygen seems to accelerate it.