Search results for "Ferrous"

showing 10 items of 75 documents

Contrasting evolution of iron phase composition in soils exposed to redox fluctuations

2018

Abstract Ferric iron (FeIII) solid phases serve many functions in soils and sediments, which include providing sorption sites for soil organic matter, nutrients, and pollutants. The reactivity of Fe solid phases depends on the mineral structure, including the overall crystallinity. In redox-active soils and sediments, repeated reductive dissolution with subsequent exposure to aqueous ferrous iron (Fe2+) and oxidative re-precipitation can alter Fe phase crystallinity and reactivity. However, the trajectory of Fe mineral transformation under redox fluctuations is unclear and has been reported to result in both increases and decreases in Fe phase crystallinity. Several factors such as water bu…

ChemistrySoil organic matterSoil classification04 agricultural and veterinary sciences010501 environmental sciences01 natural sciencesFerrousAndosolCrystallinityGeochemistry and PetrologyEnvironmental chemistrySoil water040103 agronomy & agriculture0401 agriculture forestry and fisheriesLeaching (agriculture)Dissolution0105 earth and related environmental sciencesGeochimica et Cosmochimica Acta
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Optimization of iron speciation (soluble, ferrous and ferric) in beans, chickpeas and lentils

2001

Abstract A spectrophotometric method with bathophenanthroline for iron determination that makes it possible to differentiate between iron (II) and iron (III) in total soluble iron in legumes (beans, chickpeas and lentils) was optimized. Sample size, volumes of reducing agent and bathophenanthroline were selected. Matrix interferences made it necessary to apply the addition’s method. To check the quality of the method, linearity and precision (RSD%) were determined. A linear response between 0.1 and 1.8 μg Fe/ml in the assay and precision values ranging from 2.1 to 6 for instrumental precision, and from 1.6 to 1.7 and 2.7 to 9.1, for intra- and inter-day assays, respectively were obtained. T…

ChromatographyReducing agentChemistrymedia_common.quotation_subjectMetallurgySoluble ironGeneral MedicineAnalytical ChemistryFerrousMatrix (chemical analysis)SpeciationmedicineFerricDry matterFood Sciencemedicine.drugmedia_commonFood Chemistry
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A new selective fluorogenic probe for trivalent cations.

2012

[EN] A new selective chromo-fluorogenic probe for Fe 3+, Cr 3+ and Al 3+ is reported. Detection limits are in the ¿M range and the fluorogenic sensing ability could be observed by the naked eye when illuminated with UV-light. No response is observed with divalent cations. © 2012 The Royal Society of Chemistry.

ChromiumAcetonitrilesIronComplex formationInorganic chemistryLithiumPhotochemistryArticleCatalysisDivalentSynthesischemistry.chemical_compoundQUIMICA ORGANICAUltraviolet visible spectroscopyChemical structureNickelUltraviolet spectroscopyFerric ionMaterials ChemistryFerrous ionFluoresceinFluorescent Dyeschemistry.chemical_classificationDetection limitChemistryZinc ionFerric ionQUIMICA INORGANICACopper ionMetals and AlloysComplex formationCobaltMercuryGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIlluminationSpectrometry FluorescenceZinc ionCeramics and CompositesFluoresceinSpectrophotometry UltravioletNaked eyeCadmiumAluminumChemical communications (Cambridge, England)
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Oxidation of diclofenac in the presence of iron(II) octacarboxyphthalocyanine

2021

Abstract This paper presents the results of the research on the influence of catalytic activity of iron(II) octacarboxyphthalocyanines (FePcOC) on the transformation of diclofenac (DCF) which is the most popular anti-inflammatory analgesic. Diclofenac poses a serious threat to the natural environment. The paper demonstrates that diclofenac, in the presence a monomeric form of iron octacarboxyphthalocyanine and hydroxyl radicals (HO•) (from H2O2), undergoes a transformation into diclofenac-2,5-iminoquinone (DCF-2,5-IQ), causing distinct changes in the UV–Vis absorption spectrum. In the presence of iron octacarboxyphthalocyanine and H2O2, the previously colourless diclofenac solution becomes …

Environmental EngineeringDiclofenacAbsorption spectroscopyIronHealth Toxicology and MutagenesisRadical0208 environmental biotechnology02 engineering and technology010501 environmental sciencesDFT calculations01 natural sciencesHigh-performance liquid chromatographyCatalysischemistry.chemical_compoundDiclofenacmedicineEnvironmental ChemistryFerrous Compounds0105 earth and related environmental sciencesMS analysisHplc analysisChemistryPublic Health Environmental and Occupational HealthMs analysisHydrogen PeroxideGeneral MedicineGeneral ChemistryUV–Vis spectraPollution020801 environmental engineeringTD-DFT spectraMonomerIron octacarboxyphthalocyanineHPLCOxidation-ReductionNuclear chemistrymedicine.drugChemosphere
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Mineralogy at Gusev Crater from the Mössbauer spectrometer on the Spirit Rover.

2004

Mössbauer spectra measured on Mars by the Spirit rover during the primary mission are characterized by two ferrous iron doublets (olivine and probably pyroxene) and a ferric iron doublet (tentatively associated to nanophase ferric iron oxide). Two sextets resulting from nonstoichiometric magnetite are also present, except for a coating on the rock Mazatzal, where a hematite-like sextet is present. Greater proportions of ferric-bearing phases are associated with undisturbed soils and rock surfaces as compared to fresh rock surfaces exposed by grinding. The ubiquitous presence of olivine in soil suggests that physical rather than chemical weathering processes currently dominate at Gusev crat…

Geologic SedimentsMaterials scienceExtraterrestrial EnvironmentIronMineralogyMagnesium CompoundsMarsWeatheringPyroxeneengineering.materialFerric CompoundsFerrouschemistry.chemical_compoundSpectroscopy MossbauerImpact craterComposition of MarsMagnetiteMineralsMultidisciplinaryOlivineSilicatesOxidesHematiteFerrosoferric Oxidechemistryvisual_artvisual_art.visual_art_mediumengineeringIron CompoundsScience (New York, N.Y.)
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Transformation of clay-sized minerals in soils exposed to prolonged regular alternation of redox conditions

2016

Abstract The direction of the transformation of Fe-bearing minerals under harshly changing redox conditions is still under debate. Some studies suggest preferential accumulation of weakly crystalline Fe oxides while other studies showed that repeated redox cycles favour the presence of crystalline phases. Since characterized by distinct redox cycles, paddy soils are ideal for studying redox-related transformations of Fe oxides and Fe-bearing clay minerals. We analysed changes in the Fe mineral assemblage upon long-term reduction–oxidation cycles along a chronosequence of 100, 700, and 2000-year-old paddy soils developed on comparable parent material relative to two non-irrigated counterpart…

GoethiteMineralMetallurgySoil ScienceWeathering04 agricultural and veterinary sciences010501 environmental sciencesengineering.material01 natural sciencesSilicateFerrouschemistry.chemical_compoundchemistryEnvironmental chemistryvisual_art040103 agronomy & agricultureengineeringvisual_art.visual_art_medium0401 agriculture forestry and fisheriesLepidocrociteClay mineralsSubsoil0105 earth and related environmental sciencesGeoderma
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Ligation Tunes Protein Reactivity in an Ancient Haemoglobin: Kinetic Evidence for an Allosteric Mechanism in Methanosarcina acetivorans Protoglobin

2012

Abstract: Protoglobin from Methanosarcina acetivorans (MaPgb) is a dimeric globin with peculiar structural properties such as a completely buried haem and two orthogonal tunnels connecting the distal cavity to the solvent. CO binding to and dissociation from MaPgb occur through a biphasic kinetics. We show that the heterogenous kinetics arises from binding to (and dissociation from) two tertiary conformations in ligation-dependent equilibrium. Ligation favours the species with high binding rate (and low dissociation rate). The equilibrium is shifted towards the species with low binding (and high dissociation) rates for the unliganded molecules. A quantitative model is proposed to describe t…

HEME ENVIRONMENTStereochemistrySILICA-GELSArchaeal ProteinsAllosteric regulationKineticsBiophysicslcsh:MedicinePlasma protein bindingBiochemistryDissociation (chemistry)HemoglobinsAllosteric RegulationBINDINGINTERNAL HYDROPHOBIC CAVITIESMoleculeGlobinFerrous CompoundsMethanosarcina acetivoransSettore BIO/10lcsh:ScienceBiologyT STATE HEMOGLOBINCarbon MonoxideMultidisciplinaryPhotolysisbiologyChemistryPhysicslcsh:RProteinsMethanosarcinabiology.organism_classificationRecombinant ProteinsEnzymesGlobinsKineticsOXYGEN-AFFINITYBiochemistryMethanosarcinaARABIDOPSIS-THALIANAlcsh:QGLOBIN-COUPLED SENSORSHuman medicineProtein MultimerizationLIGAND MIGRATIONNEUROGLOBINResearch ArticleProtein Binding
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Heme symmetry, vibronic structure, and dynamics in heme proteins: ferrous nicotinate horse myoglobin and soybean leghemoglobin.

2000

We report the visible and Soret absorption bands, down to cryogenic temperatures, of the ferrous nicotinate adducts of native and deuteroheme reconstituted horse heart myoglobin in comparison with soybean leghemoglobin-a. The band profile in the visible region is analyzed in terms of vibronic coupling of the heme normal modes to the electronic transition in the framework of the Herzberg–Teller approximation. This theoretical approach makes use of the crude Born–Oppenheimer states and therefore neglects the mixing between electronic and vibrational coordinates; however, it takes into account the vibronic nature of the visible absorption bands and allows an estimate of the vibronic side bands…

HemeproteinsHemeproteinBiophysicsHemePhotochemistryBiochemistryVibrationMolecular electronic transitionSpectral lineBiomaterialschemistry.chemical_compoundAnimalsFerrous CompoundsHorsesHemeMyoglobinProtein dynamicsOrganic ChemistryNicotinic AcidsTemperatureGeneral MedicineProtein Structure TertiaryLeghemoglobinVibronic couplingMyoglobinchemistrySpectrophotometryMolecular vibrationSoybeansBiopolymers
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New efficient artemisinin derived agents against human leukemia cells, human cytomegalovirus and Plasmodium falciparum: 2nd generation 1,2,4-trioxane…

2015

Abstract In our ongoing search for highly active hybrid molecules exceeding their parent compounds in anticancer, antimalaria as well as antiviral activity and being an alternative to the standard drugs, we present the synthesis and biological investigations of 2nd generation 1,2,4-trioxane-ferrocene hybrids. In vitro tests against the CCRF-CEM leukemia cell line revealed di-1,2,4-trioxane-ferrocene hybrid 7 as the most active compound (IC50 of 0.01 μM). Regarding the activity against the multidrug resistant subline CEM/ADR5000, 1,2,4-trioxane-ferrocene hybrid 5 showed a remarkable activity (IC50 of 0.53 μM). Contrary to the antimalaria activity of hybrids 4–8 against Plasmodium falciparum …

Human cytomegalovirusMetallocenesPlasmodium falciparumHeterocyclic Compounds 4 or More RingsInhibitory Concentration 50chemistry.chemical_compoundHeterocyclic CompoundsCell Line TumorDrug DiscoverymedicineHumansFerrous CompoundsArtemisininIC50HybridPharmacologyLeukemiabiologyOrganic ChemistryPlasmodium falciparumGeneral Medicinebiology.organism_classificationmedicine.diseaseVirologyArtemisininsDrug Resistance MultipleMultiple drug resistanceBiochemistryFerrocenechemistry124-Trioxanemedicine.drugEuropean Journal of Medicinal Chemistry
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Poly(N-isopropylacrylamide)-gated Fe3O4/SiO2 core shell nanoparticles with expanded mesoporous structures for the temperature triggered release of ly…

2015

Core-shell nanoparticles comprised of Fe3O4 cores and a mesoporous silica shell with an average expanded pore size of 6.07 nm and coated with a poly(N-isopropylacrylamide) (PNIPAM) layer (CS MSNs EP PNIPAM) were prepared and characterized. The nanoparticles was loaded with (Ru(bipy)3 2+) dye or an antibacterial enzyme, lysozyme, to obtain CS MSNs EP PNIPAM Ru(bipy)3 2+ and CS MSNs EP PNIPAM Lys, respectively. The lysozyme loading was determined to be 160 mg/g of nanoparticle. It was seen that Ru(bipy)3 2+ and lysozyme release was minimal at a room temperature of 25 ºC while at physiological temperature (37 º C), abrupt release was observed. The applicability of the CS MSNs EP PNIPAM Lys was…

INGENIERIA DE LA CONSTRUCCIONSilicon dioxideAcrylic ResinsBiomedical EngineeringNanoparticleBioengineeringchemistry.chemical_compoundPNIPAMQUIMICA ORGANICAColloid and Surface ChemistryBacillus cereusBIOQUIMICA Y BIOLOGIA MOLECULARNanotechnologyFerrous CompoundsPhysical and Theoretical ChemistryChemical PhysicsChromatographybiologyProtein deliveryQUIMICA INORGANICATemperatureTriggered releaseSurfaces and InterfacesGeneral MedicineChemical EngineeringMesoporous silicaSilicon Dioxidebiology.organism_classificationAnti-Bacterial AgentsMicrococcus luteuschemistryDrug deliveryPoly(N-isopropylacrylamide)NanoparticlesMuramidaseLysozymePore expansionMesoporous materialMicrococcus luteusPorosityMesoporous silicaPhysical Chemistry (incl. Structural)BiotechnologyNuclear chemistryColloids and Surfaces B: Biointerfaces
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