Search results for "fluoride"

showing 10 items of 314 documents

Real-time calibration of the A4 electromagnetic lead fluoride (PbF2) calorimeter

2011

Abstract Sufficient energy resolution is the key issue for the calorimetry in particle and nuclear physics. The calorimeter of the A4 parity violation experiment at MAMI is a segmented calorimeter where the energy of an event is determined by summing the signals of neighboring channels. In this case, the precise matching of the individual modules is crucial to obtain a good energy resolution. We have developed a calibration procedure for our total absorbing electromagnetic calorimeter which consists of 1022 lead fluoride (PbF 2 ) crystals. This procedure reconstructs the single-module contributions to the events by solving a linear system of equations, involving the inversion of a 1022×1022…

PhysicsNuclear and High Energy Physics010308 nuclear & particles physicsPhysics::Instrumentation and DetectorsLead fluorideCalorimetry[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]System of linear equations7. Clean energy01 natural sciencesParticle detectorComputational physicsCalorimeterNuclear physicsElectromagnetic calorimeter0103 physical sciencesMeasuring instrument010306 general physicsInstrumentationBeam (structure)
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Backings and targets for chemical and nuclear studies of transactinides with TASCA

2008

Abstract At GSI the gas-filled separator TASCA (TransActinide Separator and Chemistry Apparatus) was set up to investigate the chemical and physical properties of the heaviest elements making use of the highest beam intensities available [ www.gsi.de/tasca ; M. Schadel, D. Ackermann, A. Semchenkov, A. Turler, GSI Scientific Report 2005, GSI Report 2006-1, p. 262]. Appropriate backings and targets have to be developed. Conceivable backing materials are aluminium, titanium, and carbon. Aluminium backings and titanium backings in different thickness and from different companies are produced by cold rolling. Deposition by resistance heating is applied for carbon backings. For experiments in a c…

PhysicsNuclear and High Energy PhysicsMetallurgychemistry.chemical_elementTransactinide elementActinideUranium tetrafluorideUraniumNuclear physicschemistry.chemical_compoundVacuum depositionchemistryAluminiumBerylliumInstrumentationTitaniumNuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
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Observation of scattering and absorption centers in lead fluoride crystals

2006

For the first time, lead fluoride is used as a fast and compact material in electromagnetic calorimetry. Excellent optical and mechanical properties of the pure Cherenkov crystals are necessary for the A4 collaboration to perform a measurement of the nucleon's strange form factors. Visible scattering and absorption centers as well as surface damages have been investigated to characterize the quality of more than one thousand crystals. Besides, transmittance measurements have been performed on all crystals to reveal absorption bands produced by intrinsic or impurity related point-structure defects. As a consequence, 89 crystals had to be replaced by the Chinese manufacturer SICCAS.

PhysicsNuclear and High Energy PhysicsScatteringLead fluoridePhysics::OpticsFOS: Physical sciencesMolecular physicsQuality (physics)Nuclear Energy and EngineeringImpurityTransmittanceElectrical and Electronic EngineeringNuclear Experiment (nucl-ex)Absorption (electromagnetic radiation)NucleonNuclear ExperimentCherenkov radiation
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High-resolution positron lifetime spectrometer with BaF2 scintillators

1987

In this communication we report on a design of a fast coincidence positron lifetime spectrometer, which is based on single crystal barium fluoride (BaF2) scintillators. A good time resolution (190ps, FWHM), combined with a high efficiency, has been obtained in the normal experimental set-up (with cathode earthed in the photo multipliers). The pile-up effect is observed to disturbe the measured lifetimes in the 180 degree geometry due to the high detection efficiency of the BaF2 scintillator.

PhysicsPhysics and Astronomy (miscellaneous)SpectrometerPhysics::Instrumentation and Detectorsbusiness.industryBarium fluorideGeneral EngineeringGeneral ChemistryScintillatorCathodeCoincidencelaw.inventionchemistry.chemical_compoundFull width at half maximumPositronOpticschemistrylawGeneral Materials SciencebusinessSingle crystalApplied Physics A Solids and Surfaces
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High-resolution FTIR spectrum and analysis of the ν2+ν4 combination band of 32SF6

2003

Abstract The spectroscopic knowledge of sulfur hexafluoride, which is necessary for a correct remote sensing and monitoring of this species in the Earth’s atmosphere, is still very partial. In particular, the hot bands in the strongly absorbing ν 3 region (near 948 cm −1 ) have not been analyzed yet. Their study implies the analysis of many vibrational levels and thus the spectroscopy of various fundamental, harmonic, and combination bands. The present work is a new contribution to this topic, concerning the ν 2 + ν 4 combination band. The FTIR spectrum of this region has been recorded at room temperature with a resolution of 0.002 cm −1 . The data have been analyzed thanks to the HTDS soft…

PhysicsResolution (electron density)Atomic and Molecular Physics and OpticsSymmetry (physics)Sulfur hexafluoridechemistry.chemical_compoundOctahedronchemistryHarmonicMoleculePhysical and Theoretical ChemistryAtomic physicsFourier transform infrared spectroscopySpectroscopySpectroscopyJournal of Molecular Spectroscopy
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Su(4) approach to fourfold degenerate electronic states of some hexafluoride molecules

2003

Abstract We show that two appropriate realizations of the su (4) algebra allow the construction of all electronic operators needed for the study of vibronic and rovibronic interactions in a G ′ electronic state. In each case a full bosonic realization is made and all matrix elements are calculated. Illustrations of our formalism and comparisons with previous approaches are made in the case of ν 5 ( F 2 g ) and ν 3 ( F 1 u ) modes.

Physicschemistry.chemical_compoundFormalism (philosophy of mathematics)HexafluoridechemistryJahn–Teller effectQuantum mechanicsDegenerate energy levelsMoleculePhysical and Theoretical ChemistrySpectroscopyAtomic and Molecular Physics and OpticsElectronic statesJournal of Molecular Spectroscopy
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Detection of a plant enzyme exhibiting chlorogenate-dependant caffeoyltransferase activity in methanolic extracts of arbuscular mycorrhizal tomato ro…

2012

When Glomus intraradices-colonised tomato roots were extracted in methanol at 6 degrees C, chlorogenic acid (5-caffeoylquinic acid), naturally present in the extract, was slowly converted by transesterification into methyl caffeate. The progress of the reaction could be monitored by HPLC. The reaction only occurred when the ground roots were left in contact with the hydro-alcoholic extract and required the presence of 15-35% water in the mixture. When the roots were extracted in ethanol, chlorogenic acid was transformed to ethyl caffeate in the same conditions. The reaction was also detected in Glomus mosseae-colonised tomato root extracts. It was also detectable in non-mycorrhizal root ext…

Physiology[SDV]Life Sciences [q-bio]Arbuscular mycorrhizal fungiPlant SciencePlant RootsSubstrate SpecificityACBIOSYNTHESISchemistry.chemical_compoundTRANSFERASESolanum lycopersicumMycorrhizaeMethyl caffeateSWEET-POTATO ROOTSFood scienceEnzyme InhibitorsGlomusChromatography High Pressure LiquidPlant ProteinsbiologyTemperaturePlant physiologyfood and beveragesChlorogenic acidBiochemistryFUNGUSCOFFEE[SDE]Environmental SciencesGENESMETABOLISMCaffeoyltransferaseTomatoCaffeic AcidsChlorogenic acidTransferasesGenetics[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyEnzyme AssaysEthanolEsterificationPlant ExtractsfungiEthyl caffeatePlant Components Aerialbiology.organism_classificationRootsEnzyme assayEnzyme ActivationPhenylmethylsulfonyl FluorideTransesterificationchemistrybiology.proteinMethanolCAFFEIC ACIDCATALYZED SYNTHESIS
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Subsecond fluorine-19 MRI of the lung

2006

Minimal scan times in rapid fluorine-19 MRI using sulfur hexafluoride (SF6) have been on the order of 10 s. Because of the very short T1 relaxation time of SF6 (T1 = 1.65 ms), high receiver bandwidths are necessary to allow for a high number of excitations. Since high bandwidths cause high levels of electronic noise, SNR per acquisition has been too low to further reduce scan time. The purpose of this study was to investigate whether scan times could be reduced using hexafluoroethane (C2F6), a gas with a longer T1 (T1 = 7.9 ms) at a relatively low bandwidth of 488 Hz/pixel. Gradient-echo images were acquired during and after completion of the wash-in of a 70% C2F6- 30% O2 mixture. Peak SNR …

PixelSwineRapid imagingSpin–lattice relaxationContrast Mediachemistry.chemical_elementFluorineImage EnhancementMagnetic Resonance ImagingSulfur hexafluorideScan timechemistry.chemical_compoundImaging Three-DimensionalNuclear magnetic resonanceIsotopeschemistryHexafluoroethaneFluorineAnimalsRadiology Nuclear Medicine and imagingGasesLungLung ventilationMagnetic Resonance in Medicine
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Analytical challenges to determine emerging persistent organic pollutants in aquatic ecosystems

2018

Emerging persistent organic pollutants (ePOPs) include polybrominated diphenyl ethers (PBDEs) and perfluorooctane sulfonyl fluoride/perfluorooctane sulfonate (POSF/PFOS), which are newly listed in the Stockholm Convention. Other ePOPs, which have not been regulated, include organophosphate flame retardants (PFRs), novel brominated flame retardants (NBFRs) and other perfluoroalkyl substances (PFASs). Often ePOPs data related to occurrence, toxicity, impact or environmental behavior are insufficient or inadequate because of the lack of proper analytical methods to obtain them. Thus, a critical review of the analytical procedures proposed in the last six years (2011–2017) for determining ePOPs…

PollutantAquatic ecosystem010401 analytical chemistryExtraction010501 environmental sciences01 natural sciences0104 chemical sciencesAnalytical ChemistryPolybrominated diphenyl ethersPerfluoroalkyl substancesSample treatmentAquatic ecosystemsEnvironmental chemistryOrganophosphorus flame retardantsEnvironmental behaviorEmerging persistent organic pollutantsEnvironmental scienceAnalytical determinationSulfonyl fluorideSpectroscopyNovel brominated flame retardants0105 earth and related environmental sciences
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Atom transfer radical polymerization with different halides (F, Cl, Br, and I): Is the process "living" in the presence of fluorinated initiators?

2016

Atom transfer radical polymerization (ATRP) is often used for grafting from fluorinated polymers. Nevertheless, the possibility to initiate an ATRP from a C-F functionality and the activity of the catalysts in the presence of fluoride anions are essentially unexplored. Therefore, we investigated the thermodynamics and kinetics of C-F bond activation by ATRP catalysts and compared it with other halide systems. The ATRP equilibrium constant was estimated to be small for the reaction between [CuITPMA]+ and benzyl fluoride (TPMA = tris(2-pyridylmethyl)- amine). However, [CuITPMA] + could react with the more active initiator diethyl fluoromalonate (DEFM). With DEFM as initiator and CuIBr/TPMA as…

Polymers and PlasticsPOLY(VINYLIDENE FLUORIDE) ATRP HALOGEN EXCHANGE FLUORIDE INITIATORSHalide02 engineering and technologyATRP010402 general chemistry01 natural sciencesCatalysisStyreneInorganic Chemistrychemistry.chemical_compoundBenzyl fluoridePolymer chemistryFLUORIDE INITIATORSMaterials ChemistryMethyl acrylateEquilibrium constantMaterials Chemistry2506 Metals and AlloyPolymers and PlasticChemistryAtom-transfer radical-polymerizationOrganic ChemistryHALOGEN EXCHANGESettore ING-IND/27 - Chimica Industriale E Tecnologica021001 nanoscience & nanotechnology0104 chemical sciencesAmine gas treating0210 nano-technologyPOLY(VINYLIDENE FLUORIDE)
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