Search results for "IONIZATION"

showing 10 items of 1255 documents

Light Dark Matter Search with Ionization Signals in XENON1T

2019

We report constraints on light dark matter (DM) models using ionization signals in the XENON1T experiment. We mitigate backgrounds with strong event selections, rather than requiring a scintillation signal, leaving an effective exposure of (22±3) tonne day. Above ∼0.4 keVee, we observe <1 event/(tonne day keVee), which is more than 1000 times lower than in similar searches with other detectors. Despite observing a higher rate at lower energies, no DM or CEvNS detection may be claimed because we cannot model all of our backgrounds. We thus exclude new regions in the parameter spaces for DM-nucleus scattering for DM masses mχ within 3–6 GeV/c2, DM-electron scattering for mχ>30 MeV/c2, a…

Light Dark Matter TPC Ionization Axion-Like particlesCosmology and Nongalactic Astrophysics (astro-ph.CO)PhotonFOS: Physical sciencesGeneral Physics and AstronomyS030DI5S029AECAstrophysics01 natural sciencesHigh Energy Physics - ExperimentHigh Energy Physics - Experiment (hep-ex)S030DE5Ionization0103 physical sciencesionization[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex]010306 general physicsAbsorption (electromagnetic radiation)Light dark matterscintillation counterPhysicsDark Matter WIMP Dark-Matter detectors Time-projection chamber detectorsScintillationScatteringbackgrounddark matter: massphotonscatteringS029HPHS030DN5* Automatic Keywords *Scintillation counterElementary Particles and Fieldsaxion-like particles[PHYS.ASTR]Physics [physics]/Astrophysics [astro-ph]Event (particle physics)absorptionAstrophysics - Cosmology and Nongalactic Astrophysics
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High Performance Liquid Chromatografy-Mass Spectrometry based chemometric characterization of olive oils

2005

In this study the effective discrimination of extra virgin olive oils is described using HPLC-MS, combined with chemometric evaluation. The presented method is simple since the diluted oil sample is directly injected into the system, without any preliminary chemical derivatization or purification step. Separation of diacylglycerols, triacylglycerols and sterols occurs within 20 min and is achieved using an octadecyl-silica column. Detection is performed by positive APCI mass spectrometry which provided sensitivity to detect over 50 compounds in the sample. After extraction of data, stepwise discriminant function analysis is used to select the variables with the highest discriminative power.…

Linear discriminant analysiAnalytical chemistryAtmospheric-pressure chemical ionizationCross validationMass spectrometrySensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical ChemistryDiglyceridesChemometricschemistry.chemical_compoundLiquid chromatography–mass spectrometryPlant OilsDerivatizationChromatography High Pressure LiquidTriglyceridesChromatographyOrganic ChemistryOil cultivarDiscriminant AnalysisPhytosterolsReproducibility of ResultsGeneral MedicineLinear discriminant analysisHPLC–MSVegetable oilchemistryOlive oil
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Chitosomes loaded with cranberry proanthocyanidins attenuate the bacterial lipopolysaccharide-induced expression of iNOS and COX-2 in raw 264.7 macro…

2009

Chitosan binds to negatively charged soy lecithin liposomes by an electrostatic interaction driven by its positively charged amino group. This interaction allows stable covered vesicles (chitosomes) to be developed as a suitable targeted carrier and controlled release system. This study investigated the effect of chitosomes on the activation of cranberry proanthocyanidins (PAC) in Raw 264.7 macrophages. Chitosomes were characterized according to size, zeta potential, PAC-loading, and release properties. Results showed an increase in the net positive charge and size of the liposomes as the concentration of chitosan was increased, suggesting an effective covering of the vesicles by means of e…

LipopolysaccharidesLipopolysaccharideNitric Oxide Synthase Type IIPharmaceutical ScienceInflammationEndocytosisCell LineMicechemistry.chemical_compoundmedicineAnimalsMacrophageProanthocyanidinsTransport VesiclesChitosanLiposomeMolecular StructurebiologyMacrophagesVesicleControlled releaseMolecular biologyEnzyme ActivationNitric oxide synthaseVaccinium macrocarponchemistryBiochemistryCyclooxygenase 2Spectrometry Mass Matrix-Assisted Laser Desorption-Ionizationbiology.proteinmedicine.symptomJournal of Liposome Research
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Structure of a polysaccharide from the lipopolysaccharides of Vibrio vulnificus strains CECT 5198 and S3-I2-36, which is remarkably similar to the O-…

2009

High-molecular-mass polysaccharides were released by mild acid degradation of the lipopolysaccharides of two wild-type Vibrio vulnificus strain, a flagellated motile strain CECT 5198 and a non-flagellated non-motile strain S3-I2-36. Studies by sugar analysis and partial acid hydrolysis along with (1)H and (13)C NMR spectroscopies showed that the polysaccharides from both strains have the same trisaccharide repeating unit of the following structure: --4)-beta-d-GlcpNAc3NAcylAN-(1--4)-alpha-l-GalpNAmA-(1--3)-alpha-d-QuipNAc-(1--where QuiNAc stands for 2-acetamido-2,6-dideoxyglucose, GalNAmA for 2-acetimidoylamino-2-deoxygalacturonic acid, GlcNAc3NAcylAN for 2-acetamido-3-acylamino-2,3-dideoxy…

LipopolysaccharidesSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyLipopolysaccharideStereochemistryMolecular Sequence DataMalatesVibrio vulnificusPolysaccharideBiochemistryAnalytical Chemistrychemistry.chemical_compoundTrisaccharideVibrio vulnificuschemistry.chemical_classificationMolecular StructurebiologyStrain (chemistry)Polysaccharides BacterialOrganic ChemistryAbsolute configurationGeneral Medicinebiology.organism_classificationPseudoalteromonasCarbohydrate SequencechemistryBiochemistryMalic acidBacteriaCarbohydrate Research
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Core oligosaccharide of Escherichia coli B—the structure required for bacteriophage T4 recognition

2015

Abstract The structure of Escherichia coli B strain PCM 1935 core oligosaccharide has been investigated by 1H and 13C NMR spectroscopy, MALDI-TOF MS and ESI MSn. It was concluded that the core oligosaccharide is a pentasaccharide with the following structure: ESI MS/MS analysis revealed that the glycine (a minor component) is linked to the →3,7)- l -α- d -Hepp-(1→ residue.

Lipopolysaccharidesanimal structuresStereochemistryElectrospray ionizationMolecular Sequence Datamedicine.disease_causeBiochemistryAnalytical ChemistryBacteriophageResidue (chemistry)13c nmr spectroscopyEscherichia colimedicineBacteriophage T4Escherichia coliChromatographybiologyStrain (chemistry)ChemistryCore oligosaccharideOrganic ChemistryGeneral Medicinebiology.organism_classificationEscherichia coli B; Core oligosaccharide; glycine; NMR; MALDI-TOF; ESI MSCarbohydrate SequenceGlycineCarbohydrate Research
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Multinuclear magnetic resonance, electrospray ionization time-of-flight mass spectral and molecular modelling characterization of lithocholic acid am…

2003

1H, 13C and 15N NMR and electrospray ionization time-of-flight mass spectrometric characterizations of five lithocholate esters of piperazine diamides are described. Two of them are cholaphane-type cyclic structures esterified with 2,2′-bipyridine-4,4 ′ - and pyridine-2,6-dicarboxylic acid and the other three esters are open structures comprising two or four lithocholyl residues. The conformational preferences of the dimeric congeners were examined by using molecular modelling and variable-temperature 1H NMR techniques. Copyright © 2003 John Wiley & Sons, Ltd.

Lithocholic acidElectrospray ionizationchemistry.chemical_elementGeneral ChemistryCarbon-13 NMRNitrogenchemistry.chemical_compoundTime of flightPiperazinechemistryAmideProton NMROrganic chemistryGeneral Materials ScienceMagnetic Resonance in Chemistry
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13C NMR spectral assignments of 3α,3′α-bis(arylcarboxy)-5β-cholan-24-oic acid ethane-1,2-diol diesters: new lithocholic acid-based molecular clefts

1999

3α,3′α-Bis(arylcarboxy)-5β-cholan-24-oic acid ethane-1,2-diol diesters (1–3) were synthesized by the reaction of an aroyl chloride (aroyl=2,6-dichlorobenzoyl, 2-naphthoyl and 1-pyrenoyl) with lithocholic acid (3α-hydroxy-5β-cholan-24-oic acid) ethane-1,2-diol diester. The 13C NMR chemical shift assignments of the formed molecular clefts 1–3, pyrene-1-carboxylic acid methyl ester (4) (used as model compound) and 1-pyrenoyl chloride (5) are based on literature data and 13C DEPT-135, 1H,13C HMQC and 1H,13C HMBC experiments. The molecular weights of 1–3 were determined by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Copyright © 1999 John Wiley & Sons, Ltd.

Lithocholic acidMolecular massDiolGeneral ChemistryCarbon-13 NMRMass spectrometryChloridechemistry.chemical_compoundchemistryIonizationDesorptionmedicineOrganic chemistryGeneral Materials Sciencemedicine.drugMagnetic Resonance in Chemistry
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Bile acid alkylamide derivatives as low molecular weight organogelators: systematic gelation studies and qualitative structural analysis of the syste…

2011

A series of amino- and hydroxyalkyl amides of bile acids have been synthesized and characterized by Fourier transform infrared spectroscopy (FTIR), (1)H and (13)C nuclear magnetic resonance spectroscopy (NMR), as well as electrospray ionization mass spectrometry (ESI-MS) measurements. The ability of the synthesized molecules to promote gel formation was systematically investigated. Out of 396 combinations formed by 11 compounds and 36 different solvents, 22 gel-containing systems were obtained with 1% (w/v) gelator concentration. Apart from one exception, the gelator compounds were lithocholic acid derivatives. This challenges the general trend of bile acid-based physical gelators, accordin…

Lithocholic acidmedicine.drug_classSurface PropertiesElectrospray ionizationAnalytical chemistryInfrared spectroscopyMass spectrometryBiomaterialsBile Acids and Saltschemistry.chemical_compoundColloid and Surface ChemistrymedicineOrganic chemistryFourier transform infrared spectroscopyParticle SizeBile acidMolecular StructureStereoisomerismNuclear magnetic resonance spectroscopyAmidesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventMolecular WeightchemistryGelsJournal of colloid and interface science
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Photoionization of adsorbates on sites with non-axial local symmetry. An example of the symmetry group

1996

We present an analysis of the influence of the local adsorption site symmetry on the angular distribution of photoelectrons ejected from adsorbed atoms or molecules. This analysis applies to photoelectron spectra obtained with photons of any energy in the VUV (photoelectron spectroscopy) or x-ray (XPS) regions, provided that the associated wave of the electron `sees' the neighbouring surface atoms. The adsorbate - substrate system is modelled by a cluster of symmetry group consisting of an adsorbate and several atoms of the substrate. The analysis applies also to clean surfaces of symmetry and to molecules of the symmetry group fixed in space. This local symmetry analysis is an alternative …

Local symmetryChemistryPhysics::Atomic and Molecular ClustersMolecular symmetrySpherical harmonicsGeneral Materials SciencePhotoionizationSymmetry groupAtomic physicsCondensed Matter PhysicsAxial symmetrySpectral lineSymmetry (physics)Journal of Physics: Condensed Matter
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A laser desorption/resonance enhanced photoionisation TOF-system for the spatially resolved trace analysis of elements

2004

Abstract A novel method for direct and spatially resolved elemental trace analysis with high sensitivity and elemental selectivity is presented. The concept is based on the combination of a commercial MALDI-TOF mass spectrometer with a pulsed laser system for resonant postionisation of neutrals. While the MALDI method is usually applied for investigations of large organic compounds and biomolecules, the technique discussed here concerns the low mass range around 1 ⩽ A ⩽ 300. The analytical performances of the setup with respect to mass analysis, spatial resolution and overall detection efficiency are discussed.

MALDI imagingNuclear and High Energy PhysicsResolution (mass spectrometry)SpectrometerChemistryAnalytical chemistryResonancePhotoionizationMass spectrometryLaserlaw.inventionlawDesorptionInstrumentationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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