Search results for "ALLOYS"

showing 10 items of 1689 documents

Spectroelectrochemistry of cytochrome c and azurin immobilized in nanoporous antimony-doped tin oxide

2011

Stable immobilization of two redox proteins, cytochrome c and azurin, in a thin film of highly mesoporous antimony-doped tin oxide is demonstrated via UV-vis spectroscopic and electrochemical investigation.

AntimonyMaterials scienceInorganic chemistrychemistry.chemical_elementElectrochemistryRedoxCatalysisNanoporesAntimonyAzurinMaterials ChemistrybiologyNanoporousCytochrome ctechnology industry and agricultureMetals and AlloysCytochromes cTin CompoundsElectrochemical TechniquesGeneral Chemistryequipment and suppliesTin oxideSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsImmobilized ProteinschemistryCeramics and Compositesbiology.proteinSpectrophotometry UltravioletAdsorptionAzurinMesoporous materialChemical Communications
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Natural Compounds as Sustainable Additives for Biopolymers

2020

In the last few decades, the interest towards natural compounds, coming from a natural source and biodegradable, for biopolymers is always increasing because of a public request for the formulation of safe, eco-friendly, and sustainable materials. The main classes of natural compounds for biopolymers are: (i) naturally occurring fillers (nFil), such as nano-/micro- sized layered alumino-silicate: halloysite, bentonite, montmorillonite, hydroxyapatite, calcium carbonate, etc.; (ii) naturally occurring fibers (nFib), such as wood and vegetable fibers; (iii) naturally occurring antioxidant molecules (nAO), such as phenols, polyphenols, vitamins, and carotenoids. However, in this short review, …

AntioxidantPolymers and Plasticsmedicine.medical_treatmentbiopolymersReviewengineering.materialHalloysiteNatural (archaeology)lcsh:QD241-441chemistry.chemical_compoundnatural fiberslcsh:Organic chemistrybiopolymermedicineOrganic chemistryPhenolsnatural antioxidantsnatural fillerSettore CHIM/06 - Chimica OrganicaGeneral Chemistrynatural fibernatural fillersSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiMontmorilloniteCalcium carbonatechemistryPolyphenolBentoniteengineeringPolymers
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First total synthesis of antiostatin A1, a potent carbazole-based naturally occurring antioxidant.

2009

The first total synthesis of the potent antioxidant antiostatin A1 is reported, where its key features rely on a chemo- and regioselective rhodium-catalysed crossed alkyne cyclotrimerisation reaction applying functionalised ynamides and a palladium-catalysed arylamidation reaction.

Antioxidantmedicine.medical_treatmentCarbazolesAlkyneAntioxidantsCatalysischemistry.chemical_compoundAntiostatin A1Materials ChemistrymedicineOrganic chemistryRhodiumchemistry.chemical_classificationMolecular StructureCarbazoleMetals and AlloysTotal synthesisRegioselectivityStereoisomerismGeneral ChemistryKey featuresSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCyclizationCeramics and CompositesPalladiumChemical communications (Cambridge, England)
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Separation of halloysite/kaolinite mixtures in water controlled by sucrose addition: The influence of the attractive forces on the sedimentation beha…

2022

In this work, we propose an easy strategy for the separation of halloysite/kaolinite mixtures in sucrose aqueous solution. Preliminarily, we investigated the influence of the sucrose addition on the colloidal stability of kaolinite nanoplates and halloysite nanotubes (HNTs) dispersed in water. Dynamic Light Scattering (DLS) measurements revealed that the HNTs aqueous mobility is dependent on the sucrose concentration, while the ζ-potential is negligibly affected by the addition of the carbohydrate in the aqueous solvent. On the other hand, any variations on the surface charge and dynamic behavior of kaolinite were detected in the presence of sucrose. The obtained ζ-potential and DLS results…

Aqueous colloidal stabilityTGAColloid and Surface ChemistryHalloysite nanotubesNanoclaysSeparationSettore CHIM/02 - Chimica FisicaColloids and Surfaces A: Physicochemical and Engineering Aspects
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Converting p-terphenyl into a novel organo-catalyst for LED-driven energy and electron transfer photoreactions in water.

2021

p-Terphenyl is a potent photoredox catalyst under UV-irradiation. Aiming for more sustainable reaction conditions, we added two sulfonate groups to this key structure to achieve water solubility and incorporated an SO2-bridge thereby shifting the absorption spectrum towards the visible. The resulting photocatalyst shows unexpected triplet reactivity in several test reactions.

Aqueous solutionAbsorption spectroscopyMetals and AlloysGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundElectron transferSulfonatechemistryTerphenylMaterials ChemistryCeramics and CompositesPhotocatalysisReactivity (chemistry)Chemical communications (Cambridge, England)
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Mößbauer- und ESCA-Untersuchungen zur Bildung oxidischer Eisenphasen in wäßrigen Medien unter der Einwirkung organischer Korrosionsinhibitoren

1982

Korrosionsschichten auf Stahl nach Exposition in Wasser mit bestimmter Harte und Chloridgehalt wurden hinsichtlich der Wirksamkeit beigefugter organischer Inhibitoren mittels Mosbauer- und ESCA-Spektroskopie untersucht. Es entstehen relativ dicke Schichten mit einem unerwartet niedrigen Eisengehalt in Form von FeOOH. Die Schichten enthalten merkliche Mengen von Ionen aus der Testlosung und auch Abbauprodukte der Inhibitormolekule. Letztere werden anscheinend in dem korrosiven Medium zersetzt. Es ist anzunehmen, das das Gesamtmolekul zwar den Transport des Inhibitors zum Metall beeinflust, die eigentliche Inhibierung aber allein durch funktionelle Gruppen erfolgt. Mossbauer and ESCA investig…

Aqueous solutionChemistryMechanical EngineeringMetals and AlloysGeneral MedicineChlorideSurfaces Coatings and FilmsMechanics of MaterialsIron metalPolymer chemistryIron contentMössbauer spectroscopyMaterials ChemistrymedicineEnvironmental Chemistrymedicine.drugMaterials and Corrosion
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Violurato complexes of nickel(II). Formation equilibria. Deprotonation equilibria of the coordinated ligands and related stereochemical changes

1986

The formation equilibria of nickel(II) violurato-complexes in water and dimethylsulphoxide-water (80∶20) as well as deprotonation of the coordinated ligands and related stereochemical changes are reported. The stability constants of the Ni2+-H2V− complexes logβ1=5.06, Iogβ2=9.38, logβ3=12.98 as well as the acidity constants of the [Ni(H2V)3]− complex, logβj1= 8.37, logβj2=15.76, logβj3=22.37 are determined at 25 °C and 0.1M NaClO4. A new violurato-complex of Ni2+, Na4[Ni(HV)3]5H2O, is isolated and characterized.

Aqueous solutionChemistryStereochemistryOrganic solventMetals and Alloyschemistry.chemical_elementMedicinal chemistryCatalysisInorganic ChemistryNickelchemistry.chemical_compoundDeprotonationStability constants of complexesMaterials ChemistryHydrateOrganometallic chemistryTransition Metal Chemistry
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Compounds of tungsten(VI) with citric acid: A spectrophotometric, polarimetric and hydrogen-1, carbon-13 N.M.R. study of the formation and interconve…

1986

Tungsten(VI)-citrate complexes, which occur in aqueous solution, were studied by polarimetric and absorbance measurements. The pH of the medium is the principal variable controlling complex formation and interconversion equilibria. At high pH (>6), the stable complexes are monomers with 1∶2 and 1∶1 stoichiometry, depending on the tungsten(VI)-citrate ratio, while at lower pH two different dinuclear complexes are formed. The intervals of existence of these species with the pH, the number of equivalents of acid necessary for their formation, as well as the conditional stability constant, have also been calculated. The structure of these compounds have been investigated by1H and13C-n.m.r. spec…

Aqueous solutionInorganic chemistryMetals and Alloyschemistry.chemical_elementTungstenOxygenCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryStability constants of complexesMaterials ChemistryMoleculeStoichiometryOrganometallic chemistryTransition Metal Chemistry
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Complexes of molybdenum(VI) with organic diacid ligands: The molybdenum(VI)-malonic acid system

1983

Malonic acid (C3O4H4) and MoVI form in aqueous solution two dinuclear dioxo-complexes of which the stability is a function of the pH of the medium. Both complexes have a 1∶1 metal-ligand stoichiometric ratio, and the interconversion may involve a structural rearrangement. Conditional dissociation constants have been determined spectrophotometrically. Saline cryoscopy supports the spectrophotometric results. Salts of [Co(en)3]3+ have been isolated. The ligand behaviour of malonic acid differs partially from that observed for α-polyhydroxy ligands.

Aqueous solutionLigandInorganic chemistryMetals and Alloyschemistry.chemical_elementMalonic acidMedicinal chemistryCatalysisInorganic ChemistryDissociation constantchemistry.chemical_compoundchemistryMolybdenumMaterials ChemistryOrganometallic chemistryStoichiometryTransition Metal Chemistry
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Oxamidato complexes. Part 4. Electrochemical study of the copper(III)/copper(II) couple in monomeric N,N?-bis(substituent)oxamidatocopper(II) complex…

1993

The electrochemical behaviour of a series of monomeric N,N′-bis(substituent)oxamidato copper(II) complexes of formula Na2[Cu(3,5,3′,5′-X4obbz)]·4H2O [X = Cl (1), Br (2), I (3) and obbz = oxamidobis(benzoato)], Na2-[Cu(obbz)]·4H2O (4), Na2[Cu(5,5′-Me2obbz)]·4H2O (5), Na2[Cu(4,5,4,5′-(MeO)4obbz)]·4H2O(6),Na2[Cu(obp)]· 3.5H2O (7) (obp = oxamidobis(propionato)) and Na2[Cu(pba)]·6H2O (8), [pba = propylenebis(oxamate)] has been investigated by cyclic voltammetry, rotating disk electrode and coulometry in water and dimethylsulphoxide (dmso) solutions. NaNO3 (0.1 M) and n-Bu4NPF6 (0.1 M) were used as supporting electrolytes in H2O and dmso respectively, all solutions being thermostatted at 25 °C. I…

Aqueous solutionLigandOxamideInorganic chemistryMetals and AlloysSubstituentchemistry.chemical_elementMedicinal chemistryCopperInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryRotating disk electrodeCyclic voltammetryOrganometallic chemistryTransition Metal Chemistry
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