Search results for "hydroxide"

showing 10 items of 317 documents

Di- and Tri-organotin(IV) Complexes ofN-Acetyltriglycine andN-Benzoyltriglycine: Synthesis and Spectroscopic Characterization

1996

Di- and tri-organotin(IV) derivatives of N-acetyltriglycine and N-benzoyltriglycine (HA) were obtained by refluxing equimolar mixtures of the ligand and the organotin(IV) oxide or hydroxide in methanol or acetone. According to the spectroscopic data, triorganotin(IV) derivatives adopt a trigonal-bipyramidal structure in which the planar R 3 Sn IV unit is bonded by a monodentate carboxylate group and a donor group, presumably the amide C=O. The reaction of HA with the appropriate diorganotin(IV) compounds gave both dicarboxylates R 2 SnA 2 , with six-coordinated tin, and dimeric tetra-organodistannoxanes {[R 2 SnA] 2 O}2, in which the tin atoms are essentially five-coordinated.

DenticityLigandStereochemistrychemistry.chemical_elementGeneral ChemistryChemical synthesisMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryAmideHydroxideCarboxylateMethanolTinApplied Organometallic Chemistry
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Atomic-absorption spectrometric determination of calcium, magnesium and potassium in leaf samples after decomposition with molten sodium hydroxide

1991

Abstract The decomposition of standard leaf samples of varied origin and nature by fusion with sodium hydroxide in an open system has been studied. The use of sodium nitrate as an auxiliary agent facilitated the mineralization of most of the samples. The solutions obtained were analysed for calcium, magnesium and potassium by flame atomic-absorption spectrometry. The method is fast and quite precise, with absolute standard deviations of 0.04–0.13, 0.002-0.03 and 0.04–0.12% for calcium, magnesium and potassium contents of O.8-5.0, 0.13–0.48 and 0.36–2.2% respectively. The limits of detection (μg/ml) in the determination step were 0.10 for calcium, 0.011 for magnesium, and 0.09 for potassium.

Detection limitMagnesiumSodiumPotassiumAnalytical chemistrychemistry.chemical_elementCalciumAnalytical Chemistrylaw.inventionchemistry.chemical_compoundchemistrylawSodium hydroxideSodium nitrateAtomic absorption spectroscopyNuclear chemistryTalanta
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Determination of phytic acid and its degradation products by ion-pair chromatography (IPC) coupled to inductively coupled plasma-sector field-mass sp…

2004

We developed a method for the determination of phytic acid (IP6) and its degradation products (IP1-IP5) by ion-pair chromatography coupled to a double focussing inductively coupled plasma-sector field-mass spectrometer (ICP-SF-MS). For the detection of the phosphorus species a mass resolution (m/Δm) of 4000 was needed in order to separate the 31P+ signal from the interfering clusterions. The separation of the six phosphorus species was enabled by a gradient elution using tetrabutylammonium hydroxide (TBA) as ion-pair reagent. Calibration data were reported and a detection limit of 230 ng g−1 for IP6 could be obtained. The method was firstly proved for a hydrolyzate of commercially available…

Detection limitPhytic acidChromatographyTetrabutylammonium hydroxidePhosphorusfood and beverageschemistry.chemical_elementMass spectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryReagentInositolInductively coupled plasmaSpectroscopyJournal of Analytical Atomic Spectrometry
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Photo-induced chemiluminescence-based determination of diphenamid by using a multicommuted flow system

2007

This manuscript deals with the application of molecular connectivity calculations to predict the photo-induced chemiluminescent behaviour of the family of herbicides grouped as amides. Several compounds of this group were theoretically studied by means of a general discriminant equation formerly obtained, being 18 of them (plus eight from the chloroacetanilide sub-group) predicted with a high probability as photo-induced chemiluminescent. Empirical confirmation of the chemiluminometric behaviour was performed with some few commercially available amide herbicides. On the basis of these results, a new multicommutation-photo-chemiluminescent method is proposed for the determination of the diph…

Detection limitReproducibilityChromatographyChemistryAnalytical chemistryRepeatabilityAnalytical Chemistrylaw.inventionchemistry.chemical_compoundSodium hydroxidelawAmideCalibrationPhotodegradationChemiluminescenceTalanta
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Analysis of insoluble silicate: Decomposition with molten sodium hydroxide and determination of Zr(IV) with chloranilic acid in medium-strong acid

1983

A rapid, accurate and precise method for the determination of zirconium in silicates is proposed. Insoluble or sparingly soluble samples are decomposed by means of molten sodium hydroxide. Chloranilic acid is employed as reagent for the spectrophotometric determination of Zr(IV). The limit of detection is 1.2×10−7 M and the relative standard deviation is 0.24%.

Detection limitZirconiumClinical BiochemistryRelative standard deviationInorganic chemistrychemistry.chemical_elementGeneral MedicineDecompositionSilicateAnalytical Chemistrychemistry.chemical_compoundchemistryChloranilic acidSodium hydroxideReagentGeneral Materials ScienceFresenius' Zeitschrift für analytische Chemie
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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
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Thermal studies of sulphonamide derivative complexes

1991

Abstract A thermal study of a new series of acetazolamidate complexes of Co(II), Ni(II) and Cu(II) using the TG, DTG and DTA techniques in flowing air, static air and N 2 atmospheres is described. From the TG-DTG and DTA curves, different thermal behaviours can be observed. Although in all the complexes the processes of dehydration, deammination and pyrolysis can be clearly observed, in some cases they appear as several well-separated steps and, in others, as continuous stages which take place simultaneously. The differences observed between the pyrolytic decomposition in flowing air and in nitrogen are described. In flowing air, metal sulphate is formed from the thiadiazole ring, except fo…

DiethylaminePotassium hydroxidePotassiumInorganic chemistrychemistry.chemical_elementCondensed Matter PhysicsThermogravimetryMetalchemistry.chemical_compoundchemistryDifferential thermal analysisvisual_artvisual_art.visual_art_mediumPhysical and Theoretical ChemistryEthylamineInstrumentationTriethylamineThermochimica Acta
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A multi-technique, micrometer- to atomic-scale description of a synthetic analogue of chukanovite, Fe-2(CO3)(OH)(2)

2014

International audience; A synthetic analogue of chukanovite Fe-2(CO3)(OH)(2) is formed during experimental work on iron-clay interactions simulating the cooling of containers in radioactive waste repositories. Despite its small size and the mixture with other minerals it is undoubtedly identified by X-Ray Diffraction, Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy and Transmission Electron Microscopy. For the first time, the structural characterisation of a synthetic chukanovite is carried out thanks to the combination of Automated Diffraction Tomography and Precession Electron Diffraction. Refinement results and comparison with literature data show that the structure…

DiffractionMaterials scienceAutomated Diffraction Tomography; Chukanovite; Electron diffraction; Iron hydroxide carbonate; Iron-clay interaction; Nuclear waste storageScanning electron microscopeAnalytical chemistry[SDU.STU.PE]Sciences of the Universe [physics]/Earth Sciences/Petrography[SDU.STU]Sciences of the Universe [physics]/Earth Sciences02 engineering and technology010502 geochemistry & geophysics01 natural sciencesAtomic unitsMicrometreDiffraction tomographyElectron diffractionGeochemistry and Petrology[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryPrecession electron diffractionFourier transform infrared spectroscopy[SDU.STU.AG]Sciences of the Universe [physics]/Earth Sciences/Applied geologyNuclear waste storageComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesAutomated Diffraction Tomography021001 nanoscience & nanotechnologyIron hydroxide carbonateCrystallographyChukanoviteTransmission electron microscopy0210 nano-technologyIron-clay interaction[SDU.STU.MI]Sciences of the Universe [physics]/Earth Sciences/Mineralogy
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Dependence of the Lattice Parameter of Magnesium Oxide on Crystallite Size

1966

Lattice parameters were measured on MgO specimens prepared in air between 450° and 1200°C. The lattice parameter, a, decreases with increase in preparation temperature, Tp, and with increase in crystallite size. A hydroxide layer is present on the MgO particles. If MgO is prepared in vacuum, a increases as Tp increases and as crystallite size, D, increases. It is concluded that a dilatant volume stress is imposed by the hydroxide layer. It is also shown that the oxide surface reactivity toward water is linked to the deviation from perfect order ensuing from low preparation temperatures.

DilatantMaterials scienceSurface reactivityMagnesiumAnalytical chemistryOxideMineralogychemistry.chemical_elementchemistry.chemical_compoundLattice constantchemistryLattice (order)Materials ChemistryCeramics and CompositesHydroxideCrystalliteJournal of the American Ceramic Society
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A kinetic model for the oxidation of benzenethiol catalyzed by the [MoVIO2(O2CC(S)(C6H5)2)2]2− complex intercalated in a Zn(II)–Al(III) layered doubl…

2009

Abstract The heterogeneous oxidation of benzenethiol catalyzed by the dianionic bis(2-sulfanyl-2,2-diphenylethanoxycarbonyl) dioxomolybdate (VI) complex intercalated into a Zn(II)–Al(III) layered double hydroxide (LDH) host have been investigated under aerobic conditions. The kinetics of the system has been analysed in detail. In ethanol, the benzenethiol is cleanly oxidized to diphenyl disulfide in the acidic media provided by the protonic resin Amberlite IR-120(H). The reaction is second-order in benzenethiol, and the apparent rate coefficient has been found to be proportional to the catalyst weight and inversely proportional to the initial concentration of the substrate. A catalytic cycl…

Diphenyl disulfideProcess Chemistry and TechnologyInorganic chemistryComproportionationRate-determining stepMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundchemistryCatalytic cycleHydroperoxylOxidation stateHydroxidePhysical and Theoretical ChemistryJournal of Molecular Catalysis A: Chemical
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