Precision high voltage divider for the KATRIN experiment

The Karlsruhe Tritium Neutrino Experiment (KATRIN) aims to determine the absolute mass of the electron antineutrino from a precise measurement of the tritium beta-spectrum near its endpoint at 18.6 keV with a sensitivity of 0.2 eV. KATRIN uses an electrostatic retardation spectrometer of MAC-E filter type for which it is crucial to monitor high voltages of up to 35 kV with a precision and long-term stability at the ppm level. Since devices capable of this precision are not commercially available, a new high voltage divider for direct voltages of up to 35 kV has been designed, following the new concept of the standard divider for direct voltages of up to 100 kV developed at the Physikalisch-Technische Bundesanstalt (PTB). The electrical and mechanical design of the divider, the screening procedure for the selection of the precision resistors, and the results of the investigation and calibration at PTB are reported here. During the latter, uncertainties at the low ppm level have been deduced for the new divider, thus qualifying it for the precision measurements of the KATRIN experiment.Comment: 22 pages, 12 figure

The effects of activated carbon surface features on the reactive adsorption of carbamazepine and sulfamethoxazole

© 2014 Elsevier Ltd. All rights reserved.Two commercial carbons, coconut shell- and wood-based were chosen to evaluate the mechanisms of carbamazepine (CBZ) and sulfamethoxazole (SMX) adsorption from a low (ppm level) concentration of these pharmaceuticals. The initial sample and those after adsorption were extensively characterized using potentiometric titration, thermal analysis combined with mass spectroscopy, FTIR, and XPS. It was found that not only porosity but also surface chemistry plays an important role in the adsorption process. The results show that extensive surface reactions take place during adsorption and adsorbates undergo significant transformations in the pore system. The ability of carbon surfaces to form superoxide ions results in the oxidation of CBZ and SMX, and their partial decomposition. Surface chemistry also promotes dimerization of the latter species. Moreover, functional groups of CBZ and SMX, mainly amines, react with oxygen groups of the carbon surface. Thus not only microporous carbons with sizes of pores similar to those of adsorbate molecules, but the carbons with large pores, rich in oxygen groups, can efficiently remove these pharmaceuticals following the reactive adsorption mechanism

Structural transformations and disordering in zirconolite (CaZrTi2O7) at high pressure

There is interest in identifying novel materials for use in radioactive waste applications and studying their behavior under high pressure conditions. The mineral zirconolite (CaZrTi2O7) exists naturally in trace amounts in diamond-bearing deep-seated metamorphic/igneous environments, and it is also identified as a potential ceramic phase for radionuclide sequestration. However, it has been shown to undergo radiation-induced metamictization resulting in amorphous forms. In this study we probed the high pressure structural properties of this pyrochlore-like structure to study its phase transformations and possible amorphization behavior. Combined synchrotron X-ray diffraction and Raman spectroscopy studies reveal a series of high pressure phase transformations. Starting from the ambient pressure monoclinic structure, an intermediate phase with P21/m symmetry is produced above 15.6 GPa via a first order transformation resulting in a wide coexistence range. Upon compression to above 56 GPa a disordered metastable phase III with a cotunnite-related structure appears that is recoverable to ambient conditions. We examine the similarity between the zirconolite behavior and the structural evolution of analogous pyrochlore systems under pressure.<br/

Effects of NHC-Backbone Substitution on Efficiency in Ruthenium-Based Olefin Metathesis

series of ruthenium olefin metathesis catalysts bearing N-heterocyclic carbene (NHC) ligands with varying degrees of backbone and N-aryl substitution have been prepared. These complexes show greater resistance to decomposition through C−H activation of the N-aryl group, resulting in increased catalyst lifetimes. This work has utilized robotic technology to examine the activity and stability of each catalyst in metathesis, providing insights into the relationship between ligand architecture and enhanced efficiency. The development of this robotic methodology has also shown that, under optimized conditions, catalyst loadings as low as 25 ppm can lead to 100% conversion in the ring-closing metathesis of diethyl diallylmalonate

Photo-acoustic spectroscopy using a quantum cascade laser (QCL) for analysis of ammonia in water solutions

Ammonia (NH$_3$) toxicity, stemming from nitrification, can adversely affect aquatic life and influence the taste and odor of drinking water. This underscores the necessity for highly responsive and accurate sensors to continuously monitor NH$_3$ levels in water, especially in complex environments where reliable sensors have been lacking until this point. Herein, we detail the development of a sensor comprising a compact and selective analyzer with low gas consumption and a timely response, based on photoacoustic spectroscopy. This, combined with an automated liquid sampling system, enables the precise detection of ammonia traces in water. The sensor system incorporates a state-of-the art quantum cascade laser as the excitation source emitting at 9 \textmu m in resonance with the absorption line of NH$_3$ located at 1103.46 cm$^{-1}$. Our instrument demonstrated detection sensitivity at low ppm level for total ammonia nitrogen with response times less than 60 seconds. For the sampling system, an ammonia stripping solution was designed resulting in a prompt full measurement cycle (6.35 mins). A further evaluation of the sensor within a pilot study showed good reliability and agreement with the reference method for real water samples, confirming the potential of our NH$_3$ analyzer for water-quality monitoring applications.Comment: In total:15 pages,13 figures. main paper:9 pages(9 pages,9 figures:8 figures + 1 graphical abstract-figure), supporting information: 6 pages, 4 figure

Evaluation of selected chemical processes for production of low-cost silicon phase 2. silicon material task, low-cost silicon solar array project

Progress from October 1, 1977, through December 31, 1977, is reported in the design of the 50 MT/year experimental facility for the preparation of high purity silicon by the zinc vapor reduction of silicon tetrachloride in a fluidized bed of seed particles to form a free flowing granular product

FTIR quantification of industrial hydraulic fluids in perchloroethylene

The purpose of this summer research project was to investigate whether perchloroethylene can be used as a solvent for the quantitative analysis of industrial hydraulic fluids by infrared spectroscopy employing Beer's law. Standard calibration curves using carbon-hydrogen stretching (generic) and ester absorption peaks were prepared for a series of standard dilutions at low ppm levels of concentration of seven hydraulic fluids in perchloroethylene. The absorbance spectras were recorded with 1.5-10 mm fixed and variable path length sample cells made of potassium bromide. The results indicate that using ester infrared spectral peak, it is possible to detect about 20 ppm of the hydraulic fluid in perchloroethylene