The front-end electronics for the 1.8-kchannel SiPM tracking plane in the NEW detector

[EN] NEW is the first phase of NEXT-100 experiment, an experiment aimed at searching for neutrinoless double-beta decay. NEXT technology combines an excellent energy resolution with tracking capabilities thanks to a combination of optical sensors, PMTs for the energy measurement and SiPMs for topology reconstruction. Those two tools result in one of the highest background rejection potentials in the field. This work describes the tracking plane that will be constructed for the NEW detector which consists of close to 1800 sensors with a 1-cm pitch arranged in twenty- eight 64-SiPM boards. Then it focuses in the development of the electronics needed to read the 1800 channels with a front-end board that includes per-channel differential transimpedance input amplifier, gated integrator, automatic offset voltage compensation and 12-bit ADC. Finally, a de- scription of how the FPGA buffers data, carries out zero suppression and sends data to the DAQ interface using CERN RD-51 SRS s DTCC link specification complements the description of the electronics of the NEW detector tracking plane.The authors would like to acknowledge the collaboration of the membership of the NEXT experiment. The European Commision under the European Research Council 2013 Advanced Grant 339787 - NEXT, the Ministerio de Economia y Competitividad of Spain under grants CONSOLIDER-Ingenio 2010 CSD2008-0037 (CUP), FPA2009-13697-C04-04 and FIS2012-37947-C04-04 (also co-financed by FEDER). The Director, Office of Science, Office of Basic Energy Sciences, of the US Department of Energy under contract no. DE-AC02-05CH11231; and the Portuguese FCT and FEDER through the program COMPETE, project PTDC/FIS/103860/2008.Rodríguez, J.; Toledo Alarcón, JF.; Esteve Bosch, R.; Lorca, D.; Monrabal, F. (2015). The front-end electronics for the 1.8-kchannel SiPM tracking plane in the NEW detector. Journal of Instrumentation. 10:1-9. https://doi.org/10.1088/1748-0221/10/01/C01025S191

The NEXT double beta decay experiment

NEXT (Neutrino Experiment with a Xenon TPC) is a neutrinoless double- beta (ßß0¿) decay experiment at Laboratorio Subterra ´neo de Canfranc (LSC). It is an electroluminescent Time Projection Chamber filled with high pressure 136Xe gas with separated function capabilities for calorimetry and tracking. Energy resolution and background suppression are the two key features of any neutrinoless double beta decay experiment. NEXT has both good energy resolution (< 1% FWHM) and an extra handle for background identification provided by track reconstruction. We expect a background rate of 4 × 10-4 counts keV-1 kg-1 yr-1, and a sensitivity to the Majorana neutrino mass of between 80–160 meV (depending on NME) after a run of 3 effective years of the 100 kg scale NEXT-100 detector. The initial phase of NEXT-100, called NEW, is currently being commissioned at LSC. It will validate the NEXT background rate expectations and will make first measurements of the two neutrino ßß2¿ mode of 136Xe. Furthermore, the NEXT technique can be extrapolated to the tonne scale, thus allowing the full exploration of the inverted hierarchy of neutrino masses. These proceedings review NEXT R&D results, the status of detector commissioning at LSC and the NEXT physics case

Backgrounds and sensitivity of the NEXT double beta decay experiment

NEXT (Neutrino Experiment with a Xenon TPC) is a neutrinoless double-beta (ßß0¿ßß0¿) decay experiment that will operate at the Canfranc Underground Laboratory (LSC). It is an electroluminescent high-pressure gaseous xenon Time Projection Chamber (TPC) with separate read-out planes for calorimetry and tracking. Energy resolution and background suppression are the two key features of any neutrinoless double beta decay experiment. NEXT has both good energy resolution (<1% FWHM) at the Q value of 136Xe and an extra handle for background identification provided by track reconstruction. With the background model of NEXT, based on the detector simulation and the evaluation of the detector radiopurity, we can determine the sensitivity to a measurement of the ßß2¿ßß2¿ mode in NEW and to a ßß0¿ßß0¿ search in NEXT100. In this way we can predict the background rate of 5×10-4 counts/(keV kg yr)5×10-4 counts/(keV kg yr), and a sensitivity to the Majorana neutrino mass down to 100 meV after a 5-years run of NEXT100

Micromegas operation in high pressure xenon: charge and scintillation readout

The operational characteristics of a Micromegas operating in pure xenon at the pressure range of 1 to 10 bar are investigated. The maximum charge gain achieved in each pressure is approximately constant, around 4x10^2, for xenon pressures up to 5 bar and decreasing slowly above this pressure down to values somewhat above 10^2 at 10 bar. The MM presents the highest gains for xenon pressures above 4 bar, when compared to other micropattern gaseous multipliers. The lowest energy resolution obtained for X-rays of 22.1 keV exhibits a steady increase with pressure, from 12% at 1bar to about 32% at 10 bar. The effective scintillation yield, defined as the number of photons exiting through the MM mesh holes per primary electron produced in the conversion region was calculated. This yield is about 2x10^2 photons per primary electron at 1 bar, increasing to about 6x10^2 at 5 bar and, then, decreasing again to 2x10^2 at 10 bar. The readout of this scintillation by a suitable photosensor will result in higher gains but with increased statistical fluctuations.Comment: 22 pages, 11 figure

Description and commissioning of NEXT-MM prototype: first results from operation in a Xenon-Trimethylamine gas mixture

A technical description of NEXT-MM and its commissioning and first performance is reported. Having an active volume of similar to 35 cm drift x 28 cm diameter, it constitutes the largest Micromegas-read TPC operated in Xenon ever constructed, made by a sectorial arrangement of the 4 largest single wafers manufactured with the Microbulk technique to date. It is equipped with a suitably pixelized readout and with a sufficiently large sensitive volume (similar to 23 l) so as to contain long (similar to 20 cm) electron tracks. First results obtained at 1 bar for Xenon and Trymethylamine (Xe-(2%) TMA) mixture are presented. The TPC can accurately reconstruct extended background tracks. An encouraging full-width half-maximum of 11.6% was obtained for similar to 29 keV gammas without resorting to any data post-processing

Low-diffusion Xe-He gas mixtures for rare-event detection: electroluminescence yield

High pressure xenon Time Projection Chambers (TPC) based on secondary scintillation (electroluminescence) signal amplification are being proposed for rare event detection such as directional dark matter, double electron capture and double beta decay detection. The discrimination of the rare event through the topological signature of primary ionisation trails is a major asset for this type of TPC when compared to single liquid or double-phase TPCs, limited mainly by the high electron diffusion in pure xenon. Helium admixtures with xenon can be an attractive solution to reduce the electron diffu- sion significantly, improving the discrimination efficiency of these optical TPCs. We have measured the electroluminescence (EL) yield of Xe–He mixtures, in the range of 0 to 30% He and demonstrated the small impact on the EL yield of the addition of helium to pure xenon. For a typical reduced electric field of 2.5 kV/cm/bar in the EL region, the EL yield is lowered by ∼ 2%, 3%, 6% and 10% for 10%, 15%, 20% and 30% of helium concentration, respectively. This decrease is less than what has been obtained from the most recent simulation framework in the literature. The impact of the addition of helium on EL statistical fluctuations is negligible, within the experimental uncertainties. The present results are an important benchmark for the simulation tools to be applied to future optical TPCs based on Xe-He mixtures. [Figure not available: see fulltext.]

Clinical practice guidelines within the Southern African development community: a descriptive study of the quality of guideline development and concordance with best evidence for five priority diseases

<p>Abstract</p> <p>Background</p> <p>Reducing the burden of disease relies on availability of evidence-based clinical practice guidelines (CPGs). There is limited data on availability, quality and content of guidelines within the Southern African Development Community (SADC). This evaluation aims to address this gap in knowledge and provide recommendations for regional guideline development.</p> <p>Methods</p> <p>We prioritised five diseases: HIV in adults, malaria in children and adults, pre-eclampsia, diarrhoea in children and hypertension in primary care. A comprehensive electronic search to locate guidelines was conducted between June and October 2010 and augmented with email contact with SADC Ministries of Health. Independent reviewers used the AGREE II tool to score six quality domains reporting the guideline development process. Alignment of the evidence-base of the guidelines was evaluated by comparing their content with key recommendations from accepted reference guidelines, identified with a content expert, and percentage scores were calculated.</p> <p>Findings</p> <p>We identified 30 guidelines from 13 countries, publication dates ranging from 2003-2010. Overall the '<it>scope and purpose' </it>and '<it>clarity and presentation' </it>domains of the AGREE II instrument scored highest, median 58%(range 19-92) and 83%(range 17-100) respectively. '<it>Stakeholder involvement' </it>followed with median 39%(range 6-75). '<it>Applicability'</it>, '<it>rigour of development' </it>and '<it>editorial independence' </it>scored poorly, all below 25%. Alignment with evidence was variable across member states, the lowest scores occurring in older guidelines or where the guideline being evaluated was part of broader primary healthcare CPG rather than a disease-specific guideline.</p> <p>Conclusion</p> <p>This review identified quality gaps and variable alignment with best evidence in available guidelines within SADC for five priority diseases. Future guideline development processes within SADC should better adhere to global reporting norms requiring broader consultation of stakeholders and transparency of process. A regional guideline support committee could harness local capacity to support context appropriate guideline development.</p