51 research outputs found

    Measurement of the top quark mass in the tt→ dilepton channel from √s = 8 TeV ATLAS data

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    The top quark mass is measured in the ttÂŻ → dilepton channel (lepton = e,ÎŒ) using ATLAS data recorded in the year 2012 at the LHC. The data were taken at a proton proton centre-of-mass energy of √s = 8 TeV and correspond to an integrated luminosity of about 20.2 fb−1. Exploiting the template method, and using the distribution of invariant masses of lepton–b-jet pairs, the top quark mass is measured to be mtop = 172.99±0.41 (stat) ±0.74 (syst) GeV, with a total uncertainty of 0.84 GeV. Finally, a combination with previous ATLAS mtop measurements from √s = 7 TeV data in the ttÂŻ → dilepton and ttÂŻ → lepton + jets channels results in mtop = 172.84±0.34 (stat)±0.61 (syst) GeV, with a total uncertainty of 0.70 GeV

    Measurement of the cross section for isolated-photon plus jet production in pp collisions at √s=13 TeV using the ATLAS detector

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    The dynamics of isolated-photon production in association with a jet in proton–proton collisions at a centre-of-mass energy of 13 TeV are studied with the ATLAS detector at the LHC using a dataset with an integrated luminosity of 3.2 fb−1. Photons are required to have transverse energies above 125 GeV. Jets are identified using the anti- algorithm with radius parameter and required to have transverse momenta above 100 GeV. Measurements of isolated-photon plus jet cross sections are presented as functions of the leading-photon transverse energy, the leading-jet transverse momentum, the azimuthal angular separation between the photon and the jet, the photon–jet invariant mass and the scattering angle in the photon–jet centre-of-mass system. Tree-level plus parton-shower predictions from Sherpa and Pythia as well as next-to-leading-order QCD predictions from Jetphox and Sherpa are compared to the measurements

    Application of Molecular Imprinting Technique in Organophosphorus Pesticides Detection

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    International audienceMolecular imprinting technique offers a means of producing practical materials that are able to recognize a certain molecule in terms of shape, size and chemical functionality. In order to obtain a highly selective recognition of organophosphorus pesticides (OPPs), we synthesized molecularly imprinted polymers (MIPs) using pirimiphos-methyl as the template, methacrylic acid as the monomer and ethylene glycol dimethacrylate as the crosslinker. After polymerization, molecularly imprinted solid-phase extraction (MISPE) was used for the selective preconcentration of OPPs. The preparation methods and synthesis conditions of MIPs were discussed, and the specificity of MIPs and nonimprinted polymers were investigated. The results showed that MIPs enable the selective extraction of pirimiphos-methyl successfully from water sample, and demonstrated the potential of MISPE for selective and cost-effective sample pretreatment
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