Search results for "Manga"

showing 10 items of 743 documents

Enhanced flow-injection–chemiluminometric determination of sulphonamides by on-line photochemical reaction

2003

Abstract The viability of the tandem photochemical reaction-chemiluminescence detection has been studied for an heterogeneous group of sulphonamides (sulphamethoxazole, sulphadiazine, sulphamerazine, sulphamethoxypyridazine, sulphacetamide, sulphadimidine, sulphanilamide, sulphathiazole and sulphaguanidine) using sulphamethoxazole (whose chemiluminescent behaviour has not been previously reported) as a test substance. The ‘on-line’ photochemical-reaction of sulphonamides provides an enhancing influence on the chemiluminometric response of the drugs during their oxidation by potassium permanganate in sulphuric acid medium (sulphamethoxazole, sulphacetamide, sulphadimidine and sulphanilamide …

Detection limitChromatographyFluorescence spectrometryPhotochemistryBiochemistryOrders of magnitude (mass)Analytical Chemistrylaw.inventionStandard curvePotassium permanganatechemistry.chemical_compoundchemistrylawSulphaguanidineEnvironmental ChemistryPhotodegradationSpectroscopyChemiluminescenceAnalytica Chimica Acta
researchProduct

Photo-induced chemiluminescence determination of the pesticide Buminafos by a Multicommutation flow-analysis assembly

2008

Abstract The preliminary experiments in this paper deal with the photo-induced chemiluminescent behaviour of Buminafos family, after the experimental screening tests and several of them resulted positive, the herbicide Buminafos was selected to develop a new analytical method. The determination of Buminafos was performed with the aid of a Multicommutation (a solenoid valve set) assembly. The method involves the on-line photo-degradation of the analyte (stopped flow, 5 s) with the selected suitable medium (0.05% hydrogen peroxide) and its subsequent chemiluminescent oxidation by the potassium permanganate. Sample solution alternated segments with the photo-degradation medium; and, after the …

Detection limitReproducibilityAnalyteChromatographyScreening testAnalytical chemistryPesticideAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPotassium permanganatechemistrylawHydrogen peroxideChemiluminescenceTalanta
researchProduct

Some observations on the sensitivity of flow-injection techniques for atomic absorption spectrophotometry

1989

Abstract Different strategies for coupling flow-injection manifolds to atomic absorption spectrometers in order to obtain better sensitivity are compared. Using a T-connector interface, different carriers and flow compensation solvents have been assayed in an attempt to improve the sensitivity of flow-injection analysis. Manganese and copper determinations in sewage sludge have been used as a test system and the analytical parameters of both batch and flow-injection methods are compared.

Detection limitSpectrometerAnalytical chemistrychemistry.chemical_elementManganeseCopperAnalytical ChemistryVolumetric flow ratelaw.inventionchemistrylawSensitivity (control systems)Atomic absorption spectroscopySpectroscopySludgeMicrochemical Journal
researchProduct

3,3?,5,5?-Tetramethylbenzidme for the colorimetric determination of manganese in water

1998

Manganese can be determined by colorimetry with previous oxidation of Mn(II) in a strong basic medium, using 3,3′,5,5′-tetramethylbenzidine as a chromogenic reagent. The molar absorptivity of the reaction product is 3.4 × 104 mol−1l cm−1l, the detection limit 3 ng/ml, the RSD (0.5 mg/l,n = 8) 0.9% and the calibration range (1-cm cells) 0.02–0.8 mg/1 V(V), Cr(VI) and Co(II) are the most significant interferences. The new method was compared with an AAS procedure (air-acetylene flame) with previous solvent extraction and also with a colorimetric method for the determination of manganese in sea and drinking water.

Detection limitchemistryStereochemistryChromogenicReagentchemistry.chemical_elementSeawaterManganeseMolar absorptivityColorimetryAnalytical ChemistryReaction productNuclear chemistryMikrochimica Acta
researchProduct

On-line bi-directional electrostacking for As speciation/preconcentration using electrothermal atomic absorption spectrometry.

2006

A method using bi-directional electrostacking (BDES) in a flow system is presented for As preconcentration and speciation analysis. Some parameters such as electrostacking time and applied voltage, support buffers and their concentrations were investigated. Boric acid plus sodium hydroxide at 0.1mol/l concentration was selected as support buffer to improve the pre-concentration factor (PF) for As(V). An analytical range from 2.0 to 50.0mugl(-1), and 0.35mugl(-1) as limit of detection, when applied 750V for 20min, were achieved. Under these conditions, a pre-concentration factor of 4.8 was obtained. The proposed method was applied to determine As(V) in mineral water and natural water samples…

Detection limitmedia_common.quotation_subjectAnalytical chemistrychemistry.chemical_elementAnalytical Chemistrylaw.inventionBoric acidchemistry.chemical_compoundSpeciationPotassium permanganateMineral waterchemistrySodium hydroxidelawAtomic absorption spectroscopyArsenicmedia_commonTalanta
researchProduct

Ferromagnetic dinuclear mixed-valence Mn(II)/Mn(III) complexes: building blocks for the higher nuclearity complexes. structure, magnetic properties, …

2013

A series of six mixed-valence Mn(II)/Mn(III) dinuclear complexes were synthesized and characterized by X-ray diffraction. The reactivity of the complexes was surveyed, and structures of three additional trinuclear mixed-valence Mn(III)/Mn(II)/Mn(III) species were resolved. The magnetic properties of the complexes were studied in detail both experimentally and theoretically. All dinuclear complexes show ferromagnetic intramolecular interactions, which were justified on the basis of the electronic structures of the Mn(II) and Mn(III) ions. The large Mn(II)-O-Mn(III) bond angle and small distortion of the Mn(II) cation from the ideal square pyramidal geometry were shown to enhance the ferromag…

DiffractionModels MolecularManganeseValence (chemistry)Molecular StructureChemistryInorganic ChemistryCrystallographyMagnetic FieldsFerromagnetismComputational chemistryMagnetsOrganometallic CompoundsQuantum TheoryDensity functional theoryPhysical and Theoretical Chemistryta116Inorganic chemistry
researchProduct

A polymeric two-dimensional mixed-metal network. Crystal structure and magnetic properties of {[P(Ph)4][MnCr(ox)3]}

1994

Abstract The mixed-metal ferromagnet {[P(Ph) 4 ][MnCr(ox) 3 ]} n , where Ph is phenyl and ox is oxalate, has been prepared and a two-dimensional network structure, extended by Mn(II)-ox-Cr(III) bridges, has been determined from single crystal X-ray data. Crystal data: space group R 3 c , a = b =18.783(3), c =57.283(24) A, α=β=90, γ=120°, Z =24 (C 30 H 20 O 12 PCrMn). The magnetic susceptibility data obey the Curie-Weiss law in the temperature range 260–20 K with a positive Weiss constant of 10.5 K. The temperature dependence of the molar magnetization exhibits a magnetic phase transition at T c =5.9 K. The structure is discussed in relation to the strategy for preparing molecular based ferr…

Dinuclear complexesChemistryStereochemistryMagnetismMagnetismCrystal structureAtmospheric temperature rangeMagnetic susceptibilityInorganic ChemistryMagnetizationCrystallographyChromium complexesFerromagnetismddc:540Crystal structuresX-ray crystallographyMaterials ChemistryPhysical and Theoretical ChemistrySingle crystalManganese complexesInorganica Chimica Acta
researchProduct

Peculiarities of Phase Formation in Mn-Based Na SuperIonic Conductor (NaSICon) Systems: The Case of Na1+2xMnxTi2–x(PO4)3 (0.0 ≤ x ≤ 1.5)

2021

This project has received funding from the European Regional Development Fund (Project no. 01.2.2-LMT-K-718-02–0005) under grant agreement with the Research Council of Lithuania (LMTLT). We thank the High Performance Computing Center “HPC Saulėtekis” at the Faculty of Physics, Vilnius University, for the use of computational resources.

Electrode materialEnergyMaterials scienceGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_element:NATURAL SCIENCES::Physics [Research Subject Categories]Transition metalsGeneral ChemistryManganesePhosphatePhase formationArticleConductorchemistry.chemical_compoundchemistryMaterials ChemistryFast ion conductorDiffractionElectrodesMaterialsChemistry of Materials
researchProduct

Decreased Electron Transfer Rates of Manganese Porphyrins with Conformational Distortion of the Macrocycle

1998

Slow electron transfer to manganese(iii) porphyrins results when the macrocycle deviates from planarity. This was demonstrated by measuring the kinetics of homogeneous electron transfer from a series of semiquinone radical anions to synthetic manganese porphyrins (shown schematically; R1 =H, Cl, F; R2 =H, F). Three of the four porphyrins studied have nonplanar macrocycles. These results could have implications for the role of manganese in biological electron transfer processes.

Electron transferchemistrySemiquinoneHomogeneousKineticschemistry.chemical_elementGeneral ChemistryManganesePhotochemistryCatalysisPlanarity testingAngewandte Chemie International Edition
researchProduct

Representative major element compositions of clinopyroxenes and phlogopites from ultrapotassic rocks from Nangqian basin (Eastern Tibet)

2020

Representative major element compositions (in wt%) of clinopyroxenes and phlogopites from Nangqian ultrapotassic rocks. In-situ major-element compositions of mineral phases were obtained using the JEOL JXA-8230 Electron Microprobe at ISTerre, University Grenoble Alpes. Analytical conditions were 15 kV accelerating voltage and 12 nA beam current. The ZAF procedure was applied to reduce the raw data. The microprobe was calibrated using natural and synthetic standards. An X-ray element map of a calcite-bearing aggregate was acquired using 15 kV accelerating voltage and 10 nA beam current.

Elements totalMagnesium numberLongitude of eventmineralWhole-rock geochemistrySample commentElectron microprobe JEOL JXA 8230Latitude of eventcarbonate C-O isotopyChromium(III) oxideManganese oxideSodium oxideIron oxide Fe2O3Iron oxideSilicon dioxideWhole rock geochemistryAluminium oxideMagnesium number liquidtotalMagnesium oxideMineralsElectron microprobe JEOL JXA-8230Event labelcarbonate C O isotopyCalcium oxidein-situ mineral geochemistryPotassium oxideElementsin situ mineral geochemistryMagnesium number mineralChromium III oxideEarth System ResearchTitanium dioxideFe2O3
researchProduct