Search results for "medium"

showing 10 items of 3746 documents

Gadolinium-DTPA (Magnevist®) als Kontrastmittel für die arterielle DSA

1994

16 DSA investigations using intra-arterial Gd-DTPA were performed on 12 patients. The contrast medium was administered either as a 0.5 molar gadolinium solution (commercially available) or diluted with distilled water to a 0.2-0.4 molar gadolinium solution. The injection was made either by pressure injector or by hand. The aortic arch, abdominal aorta and pelvic and lower limb arteries were examined. 14 of the 16 procedures were diagnostically adequate, but compared with iodinated contrast materials, contrast was less marked. There were no cardiovascular, neurological or allergic side effects. Three patients suffered a feeling of heat and one patient had mild pain during the injection. Even…

Aortic archMolarmedicine.medical_specialtymedicine.diagnostic_testbusiness.industryGadoliniumAbdominal aortachemistry.chemical_elementIopamidolContrast mediumIodinated contrastchemistrymedicine.arteryAngiographymedicineRadiology Nuclear Medicine and imagingRadiologybusinessNuclear medicinemedicine.drugRöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren
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Selective and Efficient Removal of Mercury from Aqueous Media with the Highly Flexible Arms of a BioMOF

2016

A robust and water-stable metal-organic framework (MOF), featuring hexagonal channels decorated with methionine residues (1), selectively captures toxic species such as CH3 Hg(+) and Hg(2+) from water. 1 exhibits the largest Hg(2+) uptake capacity ever reported for a MOF, decreasing the [Hg(2+) ] and [CH3 Hg(+) ] concentrations in potable water from highly hazardous 10 ppm to the much safer values of 6 and 27 ppb, respectively. Just like with biological systems, the high-performance metal capture also involves a molecular recognition process. Both CH3 Hg(+) and Hg(2+) are efficiently immobilized by specific conformations adopted by the flexible thioether "claws" decorating the pores of 1. T…

Aqueous medium010405 organic chemistryHexagonal crystal systemChemistryInorganic chemistrychemistry.chemical_elementBiological activityGeneral Medicine02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesMercury (element)Metalchemistry.chemical_compoundPotable waterMolecular recognitionThioethervisual_artvisual_art.visual_art_medium0210 nano-technologyAngewandte Chemie International Edition
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Proton coupled electron transfer of ubiquinone Q2 incorporated in a self-assembled monolayer.

2011

We present a complete study of the reduction of ubiquinone Q(2) (UQ(2)) in simpler aqueous medium, over a pH range of 2.5 to 12.5. The short isoprenic chain ubiquinones (UQ(2)) were incorporated in a self-assembled monolayer. Under these conditions, the global 2e(-) electrochemical reaction can be described on the basis of a nine-member square scheme. The thermodynamic constants of the system were determined. The global 2e(-) process is controlled by the uptake of the second electron. The elementary electrochemical rate constants obtained by fitting of the experimental rate constant were k(s4) = 1.5 s(-1) for QH˙(+)(2)↔ QH(2), k(s5) = 1.5 s(-1) for QH˙↔ QH(-) and k(s6) = 1 s(-1) for Q˙(-)↔ …

Aqueous mediumChemistrySurface PropertiesUbiquinoneAnalytical chemistryGeneral Physics and AstronomyWaterSelf-assembled monolayerElectronHydrogen-Ion ConcentrationElectrochemistryElectron TransportReaction rate constantCoenzyme Q – cytochrome c reductaseMonolayerElectrochemistryThermodynamicsGoldPhysical and Theoretical ChemistryProton-coupled electron transferProtonsOxidation-ReductionPhysical chemistry chemical physics : PCCP
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Voltammetric behavior of berenil.

1993

Abstract Berenil is reduced on mercury drops electrode in buffered aqueous media. The reduction of —N=N— group is controlled by diffusion. Polarographie waves are of analytical usefulness. The hydrogen discharge is favored by the basic centers of the molecule in Co(ll)/ammonia-buffered media.

Aqueous mediumHydrogenAnalytical chemistryPharmaceutical Sciencechemistry.chemical_elementHydrogen-Ion ConcentrationTrypanocidal AgentsMercury (element)chemistryElectrodeElectrochemistryMoleculeVoltammetryDiminazeneElectrodesOxidation-ReductionPolarographyJournal of pharmaceutical sciences
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Concurrent removal of Cr(III), Cu(II), and Pb(II) ions from water by multifunctional TiO2/Alg/FeNPs beads

2019

Abstract The use of multifunctional materials for water remediation is a modern approach where adsorption phenomena and heterogeneous photocatalysis can be applied for the removal of pollutants. Since the ideal remediation system should be able to remove both organic and inorganic pollutants, a crucial aspect to consider is the knowledge of operational parameters affecting the removal process, especially when heavy metal ions are present in concoction as in real systems. Given the proven efficiency of multifunctional TiO2/Alg/FeNPs magnetic beads for the removal of model organic pollutants, this study investigated the possibility to exploit such system also for the removal of mixed heavy me…

Aqueous solution010405 organic chemistryMetal ions in aqueous solutionInorganic chemistryGroundwater remediationMagnetic nanoparticleAdsorbentPharmaceutical Sciencechemistry.chemical_elementManagement Monitoring Policy and Law010402 general chemistry01 natural sciencesPollution0104 chemical sciencesCatalysisMetalChromiumAdsorptionHeavy metalchemistryvisual_artPhotocatalysisvisual_art.visual_art_mediumEnvironmental ChemistryPhotocatalysis
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Symbiosis between photoactive nanoparticles and their organic ligands.

2013

Photoactive spherical metal and semiconductor nanoparticles (NPs) are smart systems that exhibit unique properties, such as a high surface-to-volume ratio, a broad absorption spectrum and size-dependent properties. They are capped with a considerable number of ligands required to give rise to stable organic and aqueous NP colloidal solutions. In addition, the ligands can also be used to introduce functionality at the NP periphery. In this case, the NP could act as a 3D-scaffold, which would make a high local concentration of a functional moiety at the NP periphery possible, moreover, the photophysical properties of the NP could be tuned. The combined action of the organic capping and the in…

Aqueous solutionAbsorption spectroscopyLigandChemistryNanoparticleNanotechnologyGeneral MedicineLigandsBiochemistryMetalColloidMicroscopy Electron Transmissionvisual_artvisual_art.visual_art_mediumMoietyMoleculeNanoparticlesSpectrophotometry UltravioletPhysical and Theoretical ChemistryOrganic ChemicalsSymbiosisPhotochemistry and photobiology
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Interaction between nitroxyl radicals and CdTe quantum dots: Determination of fluorescence-quenching mechanisms in aqueous solution

2019

Abstract The present work characterizes the optical properties of CdTe quantum dots (CdTe QDs) after interaction with nitroxyl radicals based on steady-state and time-resolved fluorescence spectroscopy studies. QDs of different sizes were exposed to 2 different nitroxyl radicals, i.e., TEMPO and 4-amino-TEMPO radicals. A clear dependence of dynamic and static Stern-Volmer constants values, KD and KS, respectively, was observed as a function of the size of QDs used, with a change from a mostly static mechanism (for smaller QD sizes) to a dynamic mechanism predominating as the nanoparticles increase in size. All observed effects are dependent on both the concentration of the radical and the s…

Aqueous solutionAqueous mediumChemistryGeneral Chemical EngineeringRadicalGeneral Physics and AstronomyNanoparticle02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesCadmium telluride photovoltaicsFluorescence spectroscopy0104 chemical sciencesNitroxyl radicalsQuantum dot0210 nano-technologyJournal of Photochemistry and Photobiology A: Chemistry
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Unusual redox play of Mo(V/IV) during oxidative aryl–aryl coupling

2012

The oxidative treatment of a suitable 1,3-diarylpropene precursor by MoCl5 causes a series of redox steps yielding a dimer of dibenzo[a,c]cycloheptene. After the oxidative aryl–aryl bond formation, a C,H activation occurs providing a tropylium intermediate. Upon aqueous workup the metal waste acts as reductive media generating the dimer in an almost quantitative manner. The oxidative generation of the tropylium species as well as the subsequent redox play by the metal waste is unique and unprecedented. The dimeric compound can be oxidatively cleaved and subsequently decarboxylated providing the key intermediate of a previous synthesis of metasequirin-B derivatives.

Aqueous solutionArylDimerOrganic ChemistryOxidative phosphorylationPhotochemistryBiochemistryRedoxMedicinal chemistryMetalchemistry.chemical_compoundchemistryvisual_artDrug Discoveryvisual_art.visual_art_mediumCyclohepteneOxidative coupling of methaneTetrahedron Letters
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An electromechanical perspective on the metal/solution interfacial region during the metallic zinc electrodeposition

2009

The difficulty of studying the metal/solution interfacial region makes the use of non-conventional measurement techniques indispensable. In this way, a careful in situ study by means of acoustic impedance techniques coupled with nano-electrogravimetric techniques allowed this interface to be monitored during the metallic zinc electrodeposition process. This paper proves the formation of a viscoelastic layer consisting of ultra-hydrated Zn(II)/Zn(I) salts as a key step in the metallic zinc electrodeposition mechanism in sulfate aqueous solutions. Surprisingly, this layer is located in the metal/solution interfacial region and not on the reaction substrate. The chloride ions effect on the met…

Aqueous solutionChemistryGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementZincElectrochemistryMetalchemistry.chemical_compoundTransition metalvisual_artElectrogravimetrySodium sulfateElectrochemistryvisual_art.visual_art_mediumLayer (electronics)Electrochimica Acta
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Application of the Generalized Molar-Ratio Method to the Determination of the Stoichiometry and Apparent Binding Constant of Nanoparticle-Organic Cap…

2015

A generalization of the molar-ratio method is applied to the determination of the stoichiometry and apparent binding constant of metal nanoparticle-organic capping complexes (MmLx) using voltammetric data for the oxygen reduction reaction (ORR) in air-saturated aqueous phosphate buffer solutions. The method is applied to the formation of binary nanohybrids consisting of gold nanoparticles (AuNPs) capped with a rigid spacer, cucurbit[7]uril (CB), termed AuNP@CB, as well as to the formation of their ternary complexes (MmLxBz) with methylene blue (MB), termed AuNP@CB@MB. The obtained stoichiometries correspond to binding of four Au surface atoms for each CB unit.

Aqueous solutionChemistryInorganic chemistryNanoparticleBinding constantAnalytical ChemistryMetalCucurbiturilColloidal goldvisual_artElectrochemistryvisual_art.visual_art_mediumTernary operationStoichiometryElectroanalysis
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