Search results for "visual_art"

showing 10 items of 2987 documents

Responses of Lumbriculus variegatus to Activated Carbon Amendments in Uncontaminated Sediments

2012

Activated carbon (AC) amendment is a recently developed sediment remediation method. The strong hydrophobic organic contaminant sorption efficiency of AC has been shown in several studies, but effects on benthic organisms require more investigation. The AC induced effects on egestion rate, growth and reproduction of Lumbriculus variegatus were studied by applying bituminous coal based AC in three different particle size fractions, namely <63 μm (90%, AC(p)), 63-200 μm (AC(m)) and 1000 μm (AC(g)), to natural uncontaminated (HS) and artificial sediment (AS). Egestion rate, growth and reproduction decreased with increasing AC concentration and finer AC particle fractions, effects being stronge…

Lumbriculus variegatusGeologic SedimentsEnvironmental remediationta1172AmendmentAdsorptionmedicineEnvironmental ChemistryAnimalsOligochaetaCharcoalEnvironmental Restoration and RemediationbiologyChemistryReproductionSedimentSorptionGeneral Chemistrybiology.organism_classificationCoalEnvironmental chemistryvisual_artCharcoalvisual_art.visual_art_mediumAdsorptionWater Pollutants ChemicalActivated carbonmedicine.drugEnvironmental Science & Technology
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Cubic and rhombohedral Ba4Lu3F17:Er3+ in transparent glass ceramics: Crystallization and upconversion luminescence

2018

CC BY-NC-ND

LuminescenceMaterials scienceGlass ceramicsBiophysicsAnalytical chemistry02 engineering and technology01 natural sciencesBiochemistrylaw.inventionlaw0103 physical sciencesActivator (phosphor):NATURAL SCIENCES:Physics [Research Subject Categories]CeramicCrystallizationThermal analysis010302 applied physicsSite-selective spectroscopyBa4Lu3F17General Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and OpticsPhoton upconversion3. Good healthNanocrystalvisual_artvisual_art.visual_art_mediumCrystallite0210 nano-technologyLuminescenceUpconversionJournal of Luminescence
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Production of methylated mercury and lead by polar macroalgae — A significant natural source for atmospheric heavy metals in clean room compartments

1998

During August and September 1995 samples of different species of macroalgae were collected from the Kongsfjord on Spitsbergen. These macroalgae were cultivated in incubation vessels under polar conditions and the releasing rates of methylated heavy metal compounds for mercury, lead and cadmium were determined. The analysis of monomethyl and dimethyl mercury was carried out by a gas chromatographic system with atomic fluorescence detection after conversion of monomethyl mercury into the volatile methylethyl mercury compound. A differential pulse anodic stripping voltammetric method was used for the determination of trimethyl lead and monomethyl cadmium, respectively. The different species of…

MERCUREFucus distichusCadmiumEnvironmental EngineeringbiologyHealth Toxicology and MutagenesisPublic Health Environmental and Occupational Healthchemistry.chemical_elementGeneral MedicineGeneral Chemistrybiology.organism_classificationPollutionMercury (element)MetalchemistryAlgaeEnvironmental chemistryvisual_artvisual_art.visual_art_mediumEnvironmental ChemistrySeawaterSolubilityChemosphere
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Rapid Evaluation of Oxidized Fatty Acid Concentration in Virgin Olive Oils Using Metal Oxide Semiconductor Sensors and Multiple Linear Regression

2009

This works aims to set up a rapid and nondestructive method to evaluate the advanced oxidation of virgin olive oils (VOOs). An electronic nose based on an array of six metal oxide semiconductor sensors was used, jointly with multiple linear regression (MLR), to predict the oxidized fatty acid (OFA) concentration in VOO samples characterized by different oxidative status. An MLR model constructed using five predictors was able to predict OFA concentration with an average validation error of 9%.

MULTIPLE LINEAR REGRESSIONBiosensing TechniquesVIRGIN OLIVE OILMetalOxide semiconductorVIRGIN OLIVE OILSMETAL OXIDE SEMICONDUCTOR SENSORSLinear regressionPlant OilsOrganic chemistryValidation errorOlive Oilchemistry.chemical_classificationChromatographyElectronic noseOXIDATIVE STATUSFatty AcidsELECTRONIC NOSEFatty acidOxidesGeneral ChemistryOXIDIZED FATTY ACIDSVegetable oilSemiconductorschemistryvisual_artLinear Modelsvisual_art.visual_art_mediumGeneral Agricultural and Biological SciencesOxidation-ReductionOlive oil
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Strain Sensing Coatings for Large Composite Structures Based on 2D MXene Nanoparticles

2021

Real-time strain monitoring of large composite structures such as wind turbine blades requires scalable, easily processable and lightweight sensors. In this study, a new type of strain-sensing coating based on 2D MXene nanoparticles was developed. A Ti3C2Tz MXene was prepared from Ti3AlC2 MAX phase using hydrochloric acid and lithium fluoride etching. Epoxy and glass fibre&ndash;reinforced composites were spray-coated using an MXene water solution. The morphology of the MXenes and the roughness of the substrate were characterised using optical microscopy and scanning electron microscopy. MXene coatings were first investigated under various ambient conditions. The coating experienced no sign…

MXenes; coatings; strain sensors; electrical properties; cyclic loadingMaterials scienceScanning electron microscopeComposite numbercoatings02 engineering and technologySurface finishengineering.materiallcsh:Chemical technology010402 general chemistry7. Clean energy01 natural sciencesBiochemistryArticleMXenesAnalytical ChemistryCoatingElectrical resistance and conductancelcsh:TP1-1185strain sensorsElectrical and Electronic EngineeringComposite materialInstrumentationcyclic loadingEpoxy021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics0104 chemical sciencesGauge factorvisual_artelectrical propertiesengineeringvisual_art.visual_art_medium0210 nano-technologyMXenesSensors
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Carbonate-coordinated metal complexes precede the formation of liquid amorphous mineral emulsions of divalent metal carbonates†

2011

During the mineralisation of metal carbonates MCO3 (M = Ca, Sr, Ba, Mn, Cd, Pb) liquid-like amorphous intermediates emerge. These intermediates that form via a liquid/liquid phase separation behave like a classical emulsion and are stabilized electrostatically. The occurrence of these intermediates is attributed to the formation of highly hydrated networks whose stability is mainly based on weak interactions and the variability of the metal-containing pre-critical clusters. Their existence and compositional freedom are evidenced by electrospray ionization mass spectrometry (ESI-MS). Liquid intermediates in non-classical crystallisation pathways seem to be more common than assumed.

Macromolecular SubstancesSurface PropertiesElectrospray ionizationInorganic chemistryCarbonatesMolecular ConformationArticlelaw.inventionMetalchemistry.chemical_compoundlawMaterials TestingGeneral Materials ScienceCrystallizationParticle SizeMineralsMineralChemistryAmorphous solidNanostructuresSolutionsMetalsvisual_artEmulsionvisual_art.visual_art_mediumCarbonateEmulsionsParticle size
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Magnetic characteristics of industrial dust from different sources of emission: A case study of Poland

2015

Abstract Dust emission and deposition in topsoil have negative effect on individual components of the ecosystem. In addition to routine geochemical analyses, magnetic measurements may provide useful complementary information related to the type, concentration and grain-size distribution of the technogenic magnetic particles (TMPs) and thus the degree of contamination of the environment. The aim of this contribution is to use magnetic parameters in distinguishing dust from a wide range of sources of air pollution (power industry, cement, coke, ceramic industries and biomass combustion). We measured magnetic susceptibility, hysteresis parameters and thermomagnetic curves. Our results suggest …

MaghemiteMineralogyThermomagnetic convectionengineering.materialHematiteCombustionMagnetic susceptibilitychemistry.chemical_compoundGeophysicsDeposition (aerosol physics)chemistryvisual_artengineeringvisual_art.visual_art_mediumMagnetic susceptibility; Hysteresis parameters; Industrial dusts; Technogenic magnetic particles; Iron oxidesEnvironmental scienceMagnetic nanoparticlesMagnetiteJournal of Applied Geophysics
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The dynamic properties of the M121H azurin metal site as studied by NMR of the paramagnetic Cu(II) and Co(II) metalloderivatives

1998

The M121H azurin mutant in solution presents various species in equilibrium that can be detected and studied by 1H NMR of the Cu(II) and Co(II) paramagnetic metalloderivatives. In both cases up to three species are observed in slow exchange, the proportions of which are different for the two metalloderivatives. Above pH 5 the major species displays a tetrahedral coordination in which the His121 can be observed as a coordinated residue. Its metal site corresponds to a new type of site that is defined as a type 1.5 site. The second and third species resemble the wild type (type 1) azurin and, above pH 4.5, they are present only at a low concentration. At low pH a protonation process increases…

Magnetic Resonance SpectroscopyChemistryInorganic chemistryWild typeElectron Spin Resonance SpectroscopyTemperatureProtonationCell BiologyNuclear magnetic resonance spectroscopyCobaltHydrogen-Ion ConcentrationBiochemistryMetalParamagnetismCrystallographyResidue (chemistry)Azurinvisual_artvisual_art.visual_art_mediumSpectrophotometry UltravioletAzurinMolecular BiologyCopperCoordination geometry
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Paramagnetic Cobalt and Nickel Derivatives of Alcaligenes denitrificans Azurin and Its M121Q Mutant. A 1H NMR Study

1996

Using cobalt or nickel to replace copper in native azurin allows one to fingerprint the metal coordination site of the protein. The metal sites of wild type Alcaligenes denitrificans azurin and its M121Q mutant are clearly distinguishable through the paramagnetic 1H NMR spectra of the Ni(II) and Co(II) derivatives. In the wild type azurin, Gly45 coordinates to nickel or cobalt, while Met121 appears as a weak metal ligand. On the contrary, in the M121Q azurin mutant, the metal exhibits a clear preference for the Gln121, which coordinates through the side chain carbonyl oxygen, and Gly45 is not a ligand. Changes in the isotropic shifts and relaxation properties of signals from the Cys112, His…

Magnetic Resonance SpectroscopyProtein ConformationStereochemistryAlcaligenes denitrificanschemistry.chemical_elementBiochemistryElectron TransportMetalAzurinNickelMetalloproteinsPoint MutationAlcaligenesPlant ProteinsBinding SitesStellacyaninMolecular StructurebiologyLigandCobaltbiology.organism_classificationNMR spectra databaseNickelchemistrySpectrophotometryvisual_artvisual_art.visual_art_mediumbiology.proteinSpectrophotometry UltravioletAzurinCobaltBiochemistry
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Metal complexes of phenobarbituric acid. Chelating behavior of the phenobarbiturate ring. Anticonvulsant properties of the K2[Cu(N-methylphenobarbitu…

1992

Abstract Na2Ni(phenobarbiturato)4·3H2O, Na2Ni3(phenobarbiturato)2(OH)6·4H2O, and NaZn(phenobarbiturato)2(OH)·H2O derivatives were prepared from Ni(II) and Zn(II) and phenobarbital. The Na2Ni(phenobarbiturato)4·3H2O complex is diamagnetic and isostructural with the complex previously reported, Na2Cu(phenobarbiturato)4, suggesting a square-planar environment around the Ni(II) ion. The DMF solutions of this complex show the existence of two species. The EPR spectra of the Cu(II) doped complex show the hyperfine and superhyperfine structures. The covalence parameters α2, β2, and δ2 show a strong bonding in the equatorial plane and suggests the formation of a [CuN4] chromophore. The anticonvulsa…

Magnetic Resonance SpectroscopyStereochemistryMephobarbitalBiochemistrylaw.inventionIonInorganic ChemistryMetalStructure-Activity RelationshiplawSeizuresAnimalsChelationIsostructuralElectron paramagnetic resonanceHyperfine structureChelating AgentsElectroshockMolecular StructureChemistryElectron Spin Resonance SpectroscopyChromophoreCrystallographyCovalent bondMetalsvisual_artPhenobarbitalvisual_art.visual_art_mediumAnticonvulsantsCopperJournal of inorganic biochemistry
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