SAF-BRET-FMEF: a developmental LMR fuel cycle facility

The SAF-BRET-FMEF complex represents a versatile fuel cycle facility for processing LMR fuel. While originally conceived for processing FFTF and CRBRP fuel, it represents a facility where LMR fuel from the first generation of innovative LMRs could be processed. The cost of transporting fuel from the LMR to the Hanford site would have to be assessed when the LMR site is identified. The throughput of BRET was set at 15 MTHM/yr during conceptual design of the facility, a rate which was adequate to process all of the fuel from FFTF and fuel and blanket material from CRBRP. The design is currently being reevaluated to see if BRET could be expanded to approx.35 MTHM/yr to process fuel and blanket material from approx.1300 MWe generating capacity of the innovative LMRs. This expanded throughput is possible by designing the equipment for an instantaneous throughput of 0.2 MTHM/d, and by selected additional modifications to the facility (e.g., expansion of shipping and receiving area, and addition of a second entry tunnel transporter), and by the fact that the LMR fuel assemblies contain more fuel than the FFTF assemblies (therefore, fewer assemblies must be handled for the same throughput). The estimated cost of such an expansion is also being assessed. As stated previously, the throughput of SAF and Fuel Assembly could be made to support typical LMRs at little additional cost. The throughput could be increased to support the fuel fabrication requirements for 1300 MWe generating capacity of the innovative LMRs. This added capacity may be achieved by increasing the number of operating shifts, and is affected by variables such as fuel design, fuel enrichment, and plutonium isotopic composition

Search for black holes and other new phenomena in high-multiplicity final states in proton-proton collisions at root s=13 TeV

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Search for heavy resonances decaying into a vector boson and a Higgs boson in final states with charged leptons, neutrinos, and b quarks

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Search for high-mass diphoton resonances in proton-proton collisions at 13 TeV and combination with 8 TeV search

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Measurement of the mass difference between top quark and antiquark in pp collisions at root s=8 TeV

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Search for leptophobic Z ' bosons decaying into four-lepton final states in proton-proton collisions at root s=8 TeV

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Digital health technologies in the accelerating medicines Partnership® Schizophrenia Program.

Although meta-analytic studies have shown that 25-33% of those at Clinical High Risk (CHR) for psychosis transition to a first episode of psychosis within three years, less is known about estimating the risk of transition at an individual level. Digital phenotyping offers a novel approach to explore the nature of CHR and may help to improve personalized risk prediction. Specifically, digital data enable detailed mapping of experiences, moods and behaviors during longer periods of time (e.g., weeks, months) and offer more insight into patterns over time at the individual level across their routine daily life. However, while novel digital health technologies open up many new avenues of research, they also come with specific challenges, including replicability of results and the adherence of participants. This paper outlines the design of the digital component of the Accelerating Medicines Partnership® Schizophrenia Program (AMP SCZ) project, a large international collaborative project that follows individuals at CHR for psychosis over a period of two years. The digital component comprises one-year smartphone-based digital phenotyping and actigraphy. Smartphone-based digital phenotyping includes 30-item short daily self-report surveys and voice diaries as well as passive data capture (geolocation, on/off screen state, and accelerometer). Actigraphy data are collected via an Axivity wristwatch. The aim of this paper is to describe the design and the three goals of the digital measures used in AMP SCZ to: (i) better understand the symptoms, real-life experiences, and behaviors of those at CHR for psychosis, (ii) improve the prediction of transition to psychosis and other health outcomes in this population based on digital phenotyping and, (iii) serve as an example for replicable and ethical research across geographically diverse regions and cultures. Accordingly, we describe the rationale, protocol and implementation of these digital components of the AMP SCZ project. **Link to video interview: https://vimeo.com/1060935583 *

Measurements of the ϒ(1S), ϒ(2S), and ϒ(3S) differential cross sections in pp collisions at s=7TeV

Differential cross sections as a function of transverse momentum pTpT are presented for the production of ϒ(nS)ϒ(nS) (n = 1, 2, 3) states decaying into a pair of muons. Data corresponding to an integrated luminosity of 4.9View the MathML sourcefb−1 in pp collisions at View the MathML sources=7TeV were collected with the CMS detector at the LHC. The analysis selects events with dimuon rapidity |y|<1.2|y|<1.2 and dimuon transverse momentum in the range View the MathML source10<pT<100GeV. The measurements show a transition from an exponential to a power-law behavior at View the MathML sourcepT≈20GeV for the three ϒ states. Above that transition, the ϒ(3S)ϒ(3S) spectrum is significantly harder than that of the ϒ(1S)ϒ(1S). The ratios of the ϒ(3S)ϒ(3S) and ϒ(2S)ϒ(2S) differential cross sections to the ϒ(1S)ϒ(1S) cross section show a rise as pTpT increases at low pTpT, then become flatter at higher pTpT