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261 result(s) for "Weinheimer, C"
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Design, construction and commissioning of a high-flow radon removal system for XENONnT
A high-flow radon removal system based on cryogenic distillation was developed and constructed to reduce radon-induced backgrounds in liquid xenon detectors for rare event searches such as XENONnT. A continuous purification of the XENONnT liquid xenon inventory of 8.4 tonnes at process flows up to 71 kg/h (200 slpm) is required to achieve a radon reduction by a factor larger than two for radon sources inside the detector. To reach such high flows, the distillation column’s design features liquid xenon inlet and outlets along with novel custom-made bath-type heat exchangers with high liquefaction capabilities. The distillation process was designed using a modification of the McCabe–Thiele approach without a bottom product extraction. The thermodynamic concept is based on a Clausius–Rankine cooling cycle with phase-changing medium, in this case the xenon itself. To drastically reduce the external cooling power requirements, an energy efficient heat pump concept was developed applying a custom-made four cylinder magnetically-coupled piston pump as compressor. The distillation system was operated at thermodynamically stable conditions at a process flow of (91±2)kg/h ((258±6) slpm), 30% over design. With this flow, a activity concentration <1μBq/kg is expected inside the XENONnT detector given the measured radon source distribution.
Current Direct Neutrino Mass Experiments
In this contribution, we review the status and perspectives of direct neutrino mass experiments, which investigate the kinematics of β-decays of specific isotopes (3H, 187Re, 163Ho) to derive model-independent information on the averaged electron (anti)neutrino mass. After discussing the kinematics of β-decay and the determination of the neutrino mass, we give a brief overview of past neutrino mass measurements (SN1987a-ToF studies, Mainz and Troitsk experiments for 3H, cryobolometers for 187Re). We then describe the Karlsruhe Tritium Neutrino (KATRIN) experiment currently under construction at Karlsruhe Institute of Technology, which will use the MAC-E-Filter principle to push the sensitivity down to a value of 200 meV (90% C.L.). To do so, many technological challenges have to be solved related to source intensity and stability, as well as precision energy analysis and low background rate close to the kinematic endpoint of tritium β-decay at 18.6 keV. We then review new approaches such as the MARE, ECHO, and Project8 experiments, which offer the promise to perform an independent measurement of the neutrino mass in the sub-eV region. Altogether, the novel methods developed in direct neutrino mass experiments will provide vital information on the absolute mass scale of neutrinos.
Improved treatment of the TFormula omitted molecular final-states uncertainties for the KATRIN neutrino-mass measurement
The KArlsruhe TRItium Neutrino experiment (KATRIN) aims to determine the effective mass of the electron antineutrino via a high-precision measurement of the tritium [Formula omitted]-decay spectrum in its end-point region. The target neutrino-mass sensitivity of [Formula omitted] at 90% CL can only be achieved in the case of high statistics and good control of the systematic uncertainties. One key systematic effect originates from the calculation of the molecular final states of T [Formula omitted] [Formula omitted] decay. In the first neutrino-mass analyses of KATRIN the contribution of the uncertainty of the molecular final-states distribution (FSD) was estimated via a conservative phenomenological approach to be [Formula omitted] In this work a new procedure is presented for estimating the FSD-related uncertainties by considering the details of the final-states calculation, i.e. the uncertainties of constants, parameters, and functions used in the calculation as well as its convergence itself as a function of the basis-set size used in expanding the molecular wave functions. The calculated uncertainties are directly propagated into the experimental observable, the squared neutrino mass [Formula omitted] and thus have to be determined individually for each experimental configuration. For the experimental conditions of the first KATRIN measurement campaign the new procedure is presented in detail, allowing for the application of this procedure to other experiments. This specific calculation leads to a constraint of the FSD-related uncertainty of [Formula omitted] well below the design limit of [Formula omitted] for any individual systematic contribution.
Improved treatment of the T2 molecular final-states uncertainties for the KATRIN neutrino-mass measurement
The KArlsruhe TRItium Neutrino experiment (KATRIN) aims to determine the effective mass of the electron antineutrino via a high-precision measurement of the tritium β -decay spectrum in its end-point region. The target neutrino-mass sensitivity of 0.2 eV / c 2 at 90% CL can only be achieved in the case of high statistics and good control of the systematic uncertainties. One key systematic effect originates from the calculation of the molecular final states of T 2 β decay. In the first neutrino-mass analyses of KATRIN the contribution of the uncertainty of the molecular final-states distribution (FSD) was estimated via a conservative phenomenological approach to be 2 × 10 - 2 eV 2 / c 4 . In this work a new procedure is presented for estimating the FSD-related uncertainties by considering the details of the final-states calculation, i.e. the uncertainties of constants, parameters, and functions used in the calculation as well as its convergence itself as a function of the basis-set size used in expanding the molecular wave functions. The calculated uncertainties are directly propagated into the experimental observable, the squared neutrino mass m ν 2 , and thus have to be determined individually for each experimental configuration. For the experimental conditions of the first KATRIN measurement campaign the new procedure is presented in detail, allowing for the application of this procedure to other experiments. This specific calculation leads to a constraint of the FSD-related uncertainty of 1.3 × 10 - 3 eV 2 / c 4 , well below the design limit of 7.5 × 10 - 3 eV 2 / c 4 for any individual systematic contribution.
Time-focusing time-of-flight, a new method to turn a MAC-E-filter into a quasi-differential spectrometer
Spectrometers based on the magnetic adiabatic collimation followed by an electrostatic filter (MAC-E-filter) principle combine high angular acceptance with an excellent energy resolution. These features make MAC-E-filters very valuable for experiments where the kinetic energy of ions or electrons from rare processes has to be measured with utmost sensitivity and precision. Examples are direct neutrino mass experiments like KATRIN which investigate the energy of electrons in the endpoint region of the tritium β -spectrum. However, the MAC-E-filter is a very sharp energy high-pass filter but not a differential spectrometer. To determine a spectral shape of a charged particle source, different electric retarding potentials have to be used sequentially, reducing the statistics. In a previous work we have shown that the advantages of the standard MAC-E-filter can be combined with a measurement of the time-of-flight (TOF), allowing to determine spectral information over a certain energy range with one retarding potential only, with the corresponding gain in statistics. This TOF method requires one to know the start time of the charged particles, which is not always possible. Therefore, we propose a new method which does not require the determination of the start time and which we call “time-focusing time-of-flight” (tfTOF): by applying a time dependent acceleration and deceleration potential at a subsequent MAC-E-filter, an energy dependent post-bunching of the charged particles is achieved.
An active transverse energy filter to differentiate low energy particles with large pitch angles in a strong magnetic field
We present the idea and proof of principle measurements for an angular-selective active filter for charged particles. The motivation for the setup arises from the need to distinguish background electrons from signal electrons in a spectrometer of MAC-E filter type. While a large fraction of the background electrons exhibit predominantly small angles relative to the magnetic guiding field (corresponding to a low amount of kinetic energy in the motion component transverse to the field lines, in the following referred to as transverse energy) and pass the filter mostly unhindered, signal electrons from an isotropically emitting source interact with the active filter and are detected. The concept is demonstrated using a microchannel plate (MCP) as an active filter element. When correctly aligned with the magnetic field, electrons with a small transverse energy pass the channels of the MCP without interaction while electrons with large transverse energies hit the channel walls and trigger an avalanche of secondary electrons that is subsequently detected. Due to several drawbacks of MCPs for an actual transverse energy filter, an alternative detection technique using microstructured Si-PIN diodes is proposed.
A pulsed, mono-energetic and angular-selective UV photo-electron source for the commissioning of the KATRIN experiment
The KATRIN experiment aims to determine the neutrino mass scale with a sensitivity of 200  meV / c 2 (90% C. L.) by a precision measurement of the shape of the tritium β -spectrum in the endpoint region. The energy analysis of the decay electrons is achieved by a MAC-E filter spectrometer. To determine the transmission properties of the KATRIN main spectrometer, a mono-energetic and angular-selective electron source has been developed. In preparation for the second commissioning phase of the main spectrometer, a measurement phase was carried out at the KATRIN monitor spectrometer where the device was operated in a MAC-E filter setup for testing. The results of these measurements are compared with simulations using the particle-tracking software “Kassiopeia”, which was developed in the KATRIN collaboration over recent years.
Magnetically-coupled piston pump for high-purity gas applications
Experiments based on noble elements such as gaseous or liquid argon or xenon utilize the ionization and scintillation properties of the target materials to detect radiation-induced recoils. A requirement for high light and charge yields is to reduce electronegative impurities well below the ppb (parts per billion, 1 ppb \\[=1\\times 10^{-9}\\] mol/mol) level. To achieve this, the target material is continuously circulated in the gas phase through a purifier and returned to the detector. Additionally, the low backgrounds necessary dictate low-Rn-emanation rates from all components that contact the gas. Since commercial pumps often introduce electronegative impurities from lubricants on internal components or through small air leaks, and are not designed to meet the radiopurity requirements, custom-built pumps are an advantageous alternative. A new pump has been developed in Muenster in cooperation with the nEXO group at Stanford University and the nEXO/XENON group at Rensselaer Polytechnic Institute based on a magnetically-coupled piston in a hermetically sealed low-Rn-emanating vessel. This pump delivers high performance for noble gases, reaching more than 210 standard liters per minute (slpm) with argon and more than 170 slpm with xenon while maintaining a compression of up to 1.9 bar, demonstrating its capability for noble gas detectors and other applications requiring high standards of gas purity.
A Critical Role for the Peroxisome Proliferator-Activated Receptor α (PPARα) in the Cellular Fasting Response: The PPARα -Null Mouse as a Model of Fatty Acid Oxidation Disorders
We hypothesized that the lipid-activated transcription factor, the peroxisome proliferator-activated receptor α (PPARα), plays a pivotal role in the cellular metabolic response to fasting. Short-term starvation caused hepatic steatosis, myocardial lipid accumulation, and hypoglycemia, with an inadequate ketogenic response in adult mice lacking PPARα (PPARα -/-), a phenotype that bears remarkable similarity to that of humans with genetic defects in mitochondrial fatty acid oxidation enzymes. In PPARα +/+ mice, fasting induced the hepatic and cardiac expression of PPARα target genes encoding key mitochondrial (medium-chain acyl-CoA dehydrogenase, carnitine palmitoyltransferase I) and extramitochondrial (acyl-CoA oxidase, cytochrome P450 4A3) enzymes. In striking contrast, the hepatic and cardiac expression of most PPARα target genes was not induced by fasting in PPARα -/- mice. These results define a critical role for PPARα in a transcriptional regulatory response to fasting and identify the PPARα -/- mouse as a potentially useful murine model of inborn and acquired abnormalities of human fatty acid utilization.
Dual Roles of Modulatory Calcineurin-Interacting Protein 1 in Cardiac Hypertrophy
The calcium/calmodulin-dependent protein phosphatase calcineurin stimulates cardiac hypertrophy in response to numerous stimuli. Calcineurin activity is suppressed by association with modulatory calcineurin-interacting protein (MCIP)1/DSCR1, which is up-regulated by calcineurin signaling and has been proposed to function in a negative feedback loop to modulate calcineurin activity. To investigate the involvement of MCIP1 in cardiac hypertrophy in vivo, we generated MCIP1 null mice and subjected them to a variety of stress stimuli that induce cardiac hypertrophy. In the absence of stress, MCIP1-/-animals exhibited no overt phenotype. However, the lack of MCIP1 exacerbated the hypertrophic response to activated calcineurin expressed from a muscle-specific transgene, consistent with a role of MCIP1 as a negative regulator of calcineurin signaling. Paradoxically, however, cardiac hypertrophy in response to pressure overload or chronic adrenergic stimulation was blunted in MCIP1-/-mice. These findings suggest that MCIP1 can facilitate or suppress cardiac calcineurin signaling depending on the nature of the hypertrophic stimulus. These opposing roles of MCIP have important implications for therapeutic strategies to regulate cardiac hypertrophy through modulation of calcineurin-MCIP activity.