Search results for "nuclear chemistry"

showing 10 items of 1124 documents

Nature of cobalt active species in hydrodesulfurization catalysis: combined support and preparation method effects

2007

Abstract Co/γ-Al2O3, Co/SiO2, Co/MCM-41, Co/ASA and Co/S2 (amorphous aluminosilicate with Al/Si = 0.13 and with Al/Si ≈ 2, respectively) were prepared by the method of wet impregnation and by the method of precipitation in the presence of sodium carbonate. The samples were characterised by XPS, XRD and TPR. The catalytic activity was tested in the hydrodesulfurization of thiophene using a continuous flow reactor. Among the wet impregnated catalysts those supported on the amorphous and ordered mesoporous silica exhibited higher HDS activity as compared to the alumina containing supports. Particularly, the use of the mesoporous, high surface area MCM-41 support, determined the best performing…

inorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementMesoporous silicaCatalysisCatalysischemistry.chemical_compoundchemistryMCM-41Physical and Theoretical ChemistrySodium carbonateMesoporous materialHydrodesulfurizationCobaltNuclear chemistry
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UraniumIV and uranyle salts, efficient and reusable catalysts for acylation of aromatic compounds

2000

Abstract Uranium tetrachloride, uranyle chloride, fluoride and also nitrate or acetate are very efficient homogeneous catalysts for the Friedel–Crafts acylation of aromatic compounds. With uranyle salts, the reaction, carried under dry air, is highly specific and the mono- or bisacylation products are obtained in high yield. Uranyle catalyst can be quantitatively recovered and reused and the organic products are obtained free of uranium.

inorganic chemicalsProcess Chemistry and TechnologyHomogeneous catalysisEtherChlorideCatalysisCatalysisAcylationchemistry.chemical_compoundchemistrymedicineOrganic chemistryPhysical and Theoretical ChemistryUranium tetrachlorideFriedel–Crafts reactionFluorideNuclear chemistrymedicine.drugJournal of Molecular Catalysis A: Chemical
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Bis[S-hexyl 3-(thiophen-2-ylmethylidene)dithiocarbazato-κ2N3,S]palladium(II)

2016

In the title complex, [Pd(C12H17N2S3)2], the PdIIatom exhibits a square-planar coordination geometry with theN,S-chelating ligands arranged in atransconfiguration. Intramolecular C—H...S hydrogen bonds are observed. In the crystal, molecules are linked by weak C—H...N hydrogen-bond interactions, forming chains parallel to thebaxis.

inorganic chemicalsQuantitative Biology::Biomoleculescrystal structureChemistryStereochemistryHydrogen bondThio-chemistry.chemical_elementGeneral MedicineCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistryhumanitiespalladium(II) complex0104 chemical sciencesCrystalTrans configurationlcsh:QD901-999lcsh:Crystallographydithiocarbazate ligandCoordination geometryPalladiumIUCrData
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Synthesis of a Tyr3-octreotate conjugated closo-carborane [HC2B10H10]: a potential compound for boron neutron capture therapy

2003

Abstract A novel Tyr 3 -octreotate conjugated closo -carborane as a potential compound for boron neutron capture therapy was obtained via Fmoc solid phase peptide synthesis. The boron cluster [C 2 B 10 H 11 ] was introduced through the reaction of 6,9-bis(acetonitrile)decaborane and 5-hexynoic acid yielding a new closo -carborane conjugated carboxylic acid which was coupled subsequently with solid phase conjugated Tyr 3 -octreotate. The final boron-containing peptide was purified by preparative reverse phase HPLC and structural identity was proved applying MALDI-TOF mass spectrometry.

inorganic chemicalschemistry.chemical_classificationOctreotateCarboxylic acidOrganic Chemistrychemistry.chemical_elementConjugated systemBiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryDecaboraneDrug DiscoveryPeptide synthesisCarboraneAcetonitrileBoronNuclear chemistryTetrahedron Letters
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Versuche zur Herstellung linolsäurearmen Ölsäureesters über eine Hydrierung mit Palladium

1980

Uber eine Hydrierung mit Palladium auf Aktivkohle konnen geringe Gehalte an Linolsaure in Gegenwart eines hohen Olsaureuberschusses recht selektiv reduziert werden. Der Linolsauregehalt eines Fettsauremethylestergemisches wurde von 10% auf 2% gesenkt, dabei entstanden 3% cis-, 4% trans-Monoenfettsauren sowie 1% Stearinsaure. The Preparation of Oleic Ester with Reduced Linoleic Acid Content by Hydrogenation with Palladium By hydrogenation with palladium on charcoal low contents of linoleic acid can be reduced quite selectively in the presence of an excess of oleic acid ester. In a mixture of fatty acid methylesters the content of linoleic acid was reduced from 10% to 2% with the formation of…

inorganic chemicalschemistry.chemical_classificationOleic acidchemistry.chemical_compoundchemistryLinoleic acidvisual_artvisual_art.visual_art_mediumFatty acidchemistry.chemical_elementCharcoalNuclear chemistryPalladiumFette, Seifen, Anstrichmittel
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Structural Characterization of Surfactant-Coated Bimetallic Cobalt/Nickel Nanoclusters by XPS, EXAFS, WAXS, and SAXS

2011

Cobalt nickel bimetallic nanoparticles were synthesized by changing the sequence of the chemical reduction of Co(II) and Ni(II) ions confined in the core of bis(2-ethylhexyl)phosphate (2)., and Ni(DEHP)(2). The reduction was carried out by mixing, sequentially or contemporaneously, fixed amounts of n-heptane solution of Co(DEHP)2 and Ni(DEHP)2 micelles with a solution of sodium borohydride in ethanol at a fixed (reductant)/(total metal) molar ratio. This procedure involves the rapid formation of surfactant-coated nanoparticles, indicated as Co/Ni (Co after Ni), Ni/Co (Ni after Co), and Co + Ni (simultaneous), followed by their slow separation as nanostructures embedded in a sodium bis(2-eth…

inorganic chemicalsendocrine systemMaterials sciencechemistry.chemical_elementNanoparticleNanoclustersMetalSodium borohydridechemistry.chemical_compoundX-ray photoelectron spectroscopyNANOPARTICLESPARTICLESBimetallic Cobalt/Nickel Nanoclusters. XPS. EXAFS. WAXS. SAXS.GOLDPhysical and Theoretical ChemistryBimetallic stripMICELLESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyNickelGeneral Energychemistryvisual_artNANOPARTICLES; PARTICLES; GOLD; MICELLESvisual_art.visual_art_mediumCobaltNuclear chemistry
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Removal of hexavalent chromium from wastewaters by bone charcoal

1999

The adsorption of hexavalent chromium onto bone charcoal was studied as a function of time, amount of charcoal, pH, concentration of chromium and sample volume. The cross interference with other elements was also investigated. Tests were carried out with solutions of chromium(VI) at concentrations between 5 and 25 mg · L–1. Chromium removal efficiencies higher than 90% were achieved at pH = 1 using 2 g of bone charcoal and a stirring time in the order of 30 min. Acid and alkaline pretreatments of bone charcoal did not improve the sorption capacity of bone charcoal against Cr(VI). The presence of other ions had practically no influence on the chromium removal. The presence of a matrix of tan…

inorganic chemicalsfood and beverageschemistry.chemical_elementMineralogySorptionrespiratory systemequipment and suppliesBiochemistryTannery effluentscarbohydrates (lipids)Matrix (chemical analysis)ChromiumSample volumechemistry.chemical_compoundAdsorptionchemistryvisual_artvisual_art.visual_art_mediumHexavalent chromiumCharcoalNuclear chemistryFresenius' Journal of Analytical Chemistry
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Hydrothermally Synthesized Strontium Peroxyapatite

2015

The current research focuses on peroxide ion incorporation in the structure of strontium hydroxyapatite (SrHAp) by exposure to H2O2 ina closed hydrothermal vessel under mild conditions at 130 to 170 °C. Peroxide enriched strontium apatite (SrPerAp) was characterized for structure by X-Ray diffraction, for peroxide content- by permanganometric titration and then viewed by SEM. This study continued from previous work that used 30%H2O2 and showed a higher included peroxide content after processing with 50% H2O2 at 130 °C 70% of the theoretical peroxide content in apatitic channels of strontium apatite. This is the highest peroxide content incorporated to date and employs a lower temperature th…

inorganic chemicalspermanganatometric titrationStrontiumInorganic chemistrystrontium peroxyapatiteGeneral Engineeringchemistry.chemical_elementhydrogen peroxideStrontium hydroxyapatitePeroxideLower temperatureApatiteHydrothermal circulationchemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumTitrationHydrogen peroxideNuclear chemistryAdvanced Materials Research
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Effect of different co-solvents on biodiesel production from various low-cost feedstocks using Sr–Al double oxides

2020

The main objective of the present paper comprises the investigation of biodiesel production from low-cost feedstock such as lard oil and waste cooking oil (WCO) using Sr-Al double oxides. Nanocatalyst was characterised FTIR, XRD, SEM, TEM, BET and XPS. The Sr:Al with 3:1 molar ratio showed the best catalytic activity in the conversion of both oils to fatty acid methyl ester. The effect of acetone and tetrahydrofuran (THF) as a co-solvent for transesterification were compared and the best result was obtained with 5 % THF. The mutual effect of the nanocatalyst and co-solvent on biodiesel production was investigated. The characterisation of biodiesel synthesised from lard oil and WCO was perfo…

kasviöljyt020209 energy02 engineering and technologyCatalysischemistry.chemical_compoundkatalyytit0202 electrical engineering electronic engineering information engineeringAcetone0601 history and archaeologySr–Al double oxidesFatty acid methyl esterBiodieselLard oil060102 archaeologyeläinrasvatRenewable Energy Sustainability and the Environmentfood and beveragesEN 1421406 humanities and the artsTransesterificationWaste cooking oilTransesterificationchemistryjätteiden hyötykäyttöBiodiesel productionnanohiukkasetMethanolBiodieselNuclear chemistry
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Rapid self-healing and anion selectivity in metallosupramolecular gels assisted by fluorine-fluorine interactions.

2017

Simple ML2 [M = Fe(II), Co(II), Ni(II)] complexes obtained from a perfluoroalkylamide derivative of 4-aminophenyl-2,2′,6,2′-terpyridine spontaneously, yet anion selectively, self-assemble into gels, which manifest an unprecedented rapid gel strength recovery, viz. self-healing, and thermal rearrangement in aqueous dimethyl sulfoxide. The key factor for gelation and rheological properties emerges from the fluorine–fluorine interactions between the perfluorinated chains, as the corresponding hydrocarbon derivative did not form metallogels. The perfluoro-terpyridine ligand alone formed single crystals, while its Fe(II), Co(II) or Ni(II) complexes underwent rapid gelation leading to highly enta…

kemiachemistry.chemical_element02 engineering and technology010402 general chemistrychemistry01 natural sciencesMetalInorganic Chemistrychemistry.chemical_compoundTheoretical and Computational ChemistryfluorinePolymer chemistryOrganic chemistryThermal stabilitymoleculeshydrocarbonsta116chemistry.chemical_classificationgeelitAqueous solutionta114Ligandmolekyylit021001 nanoscience & nanotechnologygelsfluorihiilivedyt0104 chemical sciencesHydrocarbonchemistryvisual_artFluorinevisual_art.visual_art_mediumInorganic & Nuclear Chemistry0210 nano-technologySelectivityOther Chemical SciencesDerivative (chemistry)
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