Search results for "Alate"

showing 10 items of 695 documents

Relationships between oxygen concentration and patterns of energy metabolism in the rotifer Brachionus plicatilis

1992

Abstract 1. 1. Activities of 10 enzymes and accumulation of two metabolites under experimental hypoxia were investigated in the rotifer Brachionus plicatilis . 2. 2. Pyruvate kinase (PK), lactate dehydrogenase (LDH), malic enzyme (ME), phosphoenolpyruvate carboxykinase (PEPCK), malate dehydrogenase (MDH) and fumarase (FUM) activities showed great increase at low oxygen levels. Alcohol dehydrogenase (ADH) activity was not detected. 3. 3. Alanine concentration showed an increase with low oxygen concentrations, while alanine aminotransferase (GTP) showed a slight activity increase with oxygen levels. The high alanine concentration was interpreted as enhanced proteolysis. 4. 4. Our results show…

AlaninebiologyPhysiologyMalic enzymeGeneral MedicineBrachionusbiology.organism_classificationBiochemistryMalate dehydrogenasechemistry.chemical_compoundBiochemistrychemistryLactate dehydrogenasebiology.proteinLimiting oxygen concentrationMolecular BiologyPyruvate kinaseAlcohol dehydrogenaseComparative Biochemistry and Physiology Part B: Comparative Biochemistry
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Improved (photo)catalytic propene hydration in a gas/solid system by using heteropolyacid/oxide composites: Electron paramagnetic resonance, acidity,…

2017

Binary materials composed of the oxides SiO2, TiO2 and N-doped TiO2 and the Keggin heteropolyacid (PW12) were prepared and physicochemically characterized. They were used as catalysts and photocatalysts for the hydration of propene to 2-propanol. The characterization of the samples, particularly the electron paramagnetic resonance (EPR) spectroscopy results and the acidity properties, were useful to explain the key role played by the PW12 in the composite materials in the thermal and photoassisted catalytic processes. The simultaneous pres-ence of heat and UV light improved the activity of PW12 in the thermal process, and the binary materials showed better (photo)catalytic activities than t…

AlkeneOxideHydrationHeteropolyacids02 engineering and technologyAlkenes010402 general chemistryHeterogeneous catalysis01 natural sciencesAlkenes Heterogeneous catalysis Heteropolyacids Hydration Photocatalysis PolyoxometalatesCatalysislaw.inventionPropeneInorganic Chemistrychemistry.chemical_compoundHeterogeneous catalysiPhotocatalysilawReactivity (chemistry)PhotocatalysisComposite materialElectron paramagnetic resonanceHeterogeneous catalysisPolyoxometalatePolyoxometalatesAlkenes; Heterogeneous catalysis; Heteropolyacids; Hydration; Photocatalysis; PolyoxometalatesHeteropolyacid021001 nanoscience & nanotechnology0104 chemical sciencesCharacterization (materials science)chemistryPhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technology
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All-Optical frequency Shifter in a Periodically Poled Lithium Tantalate Waveguide

2011

A frequency shifting device is fabricated and tested in a congruent Lithium Tantalate waveguide. Periodic poling for quasi-phase-matching and channels for operation in the near-infrared C-band were obtained, demonstrating a two-stage parametric conversion.

All-optical wavelength conversion second-harmonic generation difference-frequency generation ferroelectric crystals periodic poling Lithium Tantalate Lithium Niobate.Settore ING-INF/02 - Campi ElettromagneticiSettore ING-INF/01 - Elettronica
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Transport of C(4)-dicarboxylates in Wolinella succinogenes.

2000

ABSTRACT C 4 -dicarboxylate transport is a prerequisite for anaerobic respiration with fumarate in Wolinella succinogenes , since the substrate site of fumarate reductase is oriented towards the cytoplasmic side of the membrane. W. succinogenes was found to transport C 4 -dicarboxylates (fumarate, succinate, malate, and aspartate) across the cytoplasmic membrane by antiport and uniport mechanisms. The electrogenic uniport resulted in dicarboxylate accumulation driven by anaerobic respiration. The molar ratio of internal to external dicarboxylate concentration was up to 10 3 . The dicarboxylate antiport was either electrogenic or electroneutral. The electroneutral antiport required the prese…

Anaerobic respirationAntiporterPhysiology and MetabolismMutantMalatesBiologymedicine.disease_causeMicrobiologyCell membraneElectron TransportOxygen ConsumptionBacterial ProteinsFumaratesRespirationmedicineDicarboxylic AcidsAnaerobiosisMolecular BiologyEscherichia coliDicarboxylic Acid TransportersAspartic AcidNitratesEscherichia coli ProteinsCell MembraneSodiumMembrane ProteinsBiological TransportSuccinatesFumarate reductaseElectron transport chainWolinellamedicine.anatomical_structureBiochemistryMutagenesisCarrier ProteinsGene DeletionJournal of bacteriology
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A highly enantioselective abiotic receptor for malate dianion in aqueous solution

2006

The highly enantioselective molecular recognition of the malate dianion by a synthetic receptor in aqueous solution has been studied by potentiometric titrations, mass spectrometry (ESI-MS), diffusion measurements (PGSE NMR) and molecular modeling. Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es

AnionsModels MolecularMalate dianionSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyMolecular modelUNESCO::QUÍMICADiffusionPotentiometric titrationMalatesMolecular modelingAbiotic receptorMass spectrometry:QUÍMICA [UNESCO]CatalysisSubstrate SpecificityMolecular recognitionComputational chemistryMaterials ChemistryOrganic chemistryAqueous solutionReceptorAbiotic componentEnantioselectiveAqueous solutionMolecular StructureChemistrySpectrometryMeasurementsMetals and AlloysEnantioselective synthesisWaterHydrogen BondingStereoisomerismGeneral ChemistryGeneral MedicineUNESCO::QUÍMICA::Química macromolecularCombinatorial chemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolutionsCeramics and CompositesPotentiometryEnantioselective ; Abiotic receptor ; Malate dianion ; Aqueous solution ; Spectrometry ; Measurements ; Molecular modeling:QUÍMICA::Química macromolecular [UNESCO]
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Microporous alumina membranes electrochemically grown

2003

Abstract The electrochemical fabrication of alumina membranes by anodizing of aluminium in phosphoric acid and oxalic acid solutions, in the temperature interval from −1 to 16 °C, was investigated in order to study the influence of different parameters (initial treatment of aluminium surface, nature and composition of electrolyte, temperature) on the final characteristics of the membranes. Porous layers were grown using a linear potential scan at 0.2 V s −1 up to 160 V in H 3 PO 4 solution and 70 V in oxalic acid solution. The efficiency of porous layer formation was calculated by using Faraday's law and weight measurements. Pore size distribution and porosity of membranes prepared in 0.4 M…

AnodizingGeneral Chemical EngineeringOxalic acidInorganic chemistrychemistry.chemical_elementElectrolyteOxalatechemistry.chemical_compoundAluminium anodizing Anodic porous oxide Ceramic membrane Membrane preparation Porous aluminaCeramic membraneMembranechemistryAluminiumElectrochemistryPhosphoric acidElectrochimica Acta
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Anhydrous Amorphous Calcium Oxalate Nanoparticles from Ionic Liquids: Stable Crystallization Intermediates in the Formation of Whewellite

2015

The mechanisms by which amorphous intermediates transform into crystalline materials are not well understood. To test the viability and the limits of the classical crystallization, new model systems for crystallization are needed. With a view to elucidating the formation of an amorphous precursor and its subsequent crystallization, the crystallization of calcium oxalate, a biomineral widely occurring in plants, is investigated. Amorphous calcium oxalate (ACO) precipitated from an aqueous solution is described as a hydrated metastable phase, as often observed during low-temperature inorganic synthesis and biomineralization. In the presence of water, ACO rapidly transforms into hydrated whewe…

Aqueous solutionChemistryWhewelliteOrganic ChemistryCalcium oxalateGeneral Chemistryengineering.materialCatalysislaw.inventionAmorphous solidchemistry.chemical_compoundChemical engineeringlawengineeringAnhydrousWater of crystallizationOrganic chemistryCrystallizationDissolutionChemistry - A European Journal
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Study of the interaction between [Cu(bipy)]2+ and oxalate in dimethyl sulfoxide. Crystal structure of [Cu2(bipy)2(H2O)2ox]SO4·[Cu(bipy)ox]

1991

Abstract A study of complex formation between [Cu(bipy)]2+ and ox2− (bipy and ox2− being 2,2′-bipyridyl and the dianion of oxalic acid), has been carried out by potentiometry in dimethyl sulfoxide solution. The constants of the equilibria and are log β110 = 11.165(1) and log β210 = 13.185(5) at 25 °C and 0.1 mol dm−3 tetra-n- butylammonium perchlorate. The high values of these constants are consistent with the symmetrical bidentate and bis-bidentate modes of oxalate in [Cu(bipy)ox] and [Cu2(bipy)2ox]2+ units, respectively, as shown by X-ray diffraction studies. Well-formed single crystals of [Cu2(bipy)2(H2O)2ox]SO4· [Cu(bipy)ox] were grown from aqueous solutions and characterized by X-ray d…

Aqueous solutionDenticityChemistryInorganic chemistrychemistry.chemical_elementCrystal structureCopperOxalateInorganic ChemistryPerchloratechemistry.chemical_compoundCrystallographyMaterials ChemistryMoleculePhysical and Theoretical ChemistryMonoclinic crystal systemInorganica Chimica Acta
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Oxalate and 2,2′-bipyrimidine as bis-chelating ligands in the honeycomb layered compound {[Fe2(bpym)(ox)2]·5H2O}n

2002

The novel two-dimensional iron(II) compound of formula {[Fe2(bpym)(ox)2]·5H2O}n (1) [bpym = 2,2′-bipyrimidine and ox = oxalate dianion] is obtained by reaction of oxalic acid, iron(II) chloride and 2,2′-bipyrimidine in aqueous solution. The structure of 1 is made up of oxalato-bridged iron(II) chains cross-linked by bischelating bpym affording a honeycomb lattice. Variable-temperature magnetic susceptibility data of 1 show the occurrence of relatively large antiferromagnetic interactions between the high spin iron(II) ions separated by more than 5.5 A through bridging bpym [Jbpym = −4.0(2) cm−1] and ox [Jox = ca. −7.8(2) cm−1] ligands. These values compare well with those obtained in the ir…

Aqueous solutionDenticityChemistryLigandInorganic chemistryOxalic acidGeneral ChemistryChlorideMagnetic susceptibilityCatalysisOxalateCrystallographychemistry.chemical_compoundMaterials ChemistrymedicineAntiferromagnetismmedicine.drugNew Journal of Chemistry
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Oxidation of oxalate ion in aqueous suspensions of TiO2 by photocatalysis and ozonation

2005

Abstract Oxalate anion has been oxidized in aqueous alkaline solution by using ozonation and photocatalysis in the presence of TiO 2 . A batch annular reactor has been used for carrying out reactivity runs in the presence of air/ozone, air/ozone/near UV irradiation, air/ozone/TiO 2 , air/near UV-irradiated TiO 2 and air/ozone/near UV-irradiated TiO 2 . The Langmuir–Hinshelwood kinetic model adequately describes the photocatalytic results obtained at different reaction conditions and allows determining the values of the kinetic and equilibrium adsorption constants. The contemporary presence of photocatalysis and ozonation shows a significant improvement of the process performance as the oxid…

Aqueous solutionOzoneRadicalInorganic chemistryGeneral ChemistryPhotochemistryCatalysisOxalateCatalysisOzonizationchemistry.chemical_compoundOzoneAdsorptionchemistrysingle ozonationPhotocatalysisReactivity (chemistry)Catalysis Today
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