Search results for "nanotechnology"

showing 10 items of 9818 documents

Electrochemical and bioelectrocatalytical properties of novel block-copolymers containing interacting ferrocenyl units

2008

The electrochemical characterization of three different polystyrene-b-polybutadiene block-copolymers, functionalized with diferrocenylsilane units, is reported. The PB-blocks have been functionalized with different fractions of electronicall y communicated, PSm-PB„ p (HSiMeFc2)p units, where m = 615, n = 53, p = 39 (1), m = 375, n = 92, p = 76 (2) and m = 455, n = 204, p = 170 (3). Electrochemical character­ ization has been carried out both in solution and after electrochemical deposition onto platinum electrodes. The bioelectrocatalytical properties of electrodes modified with the polymers in the nicotinamide dinucleotide (NADH) and glucose oxidase (GOx) oxidations have been investigated …

chemistry.chemical_element02 engineering and technology010402 general chemistryElectrochemistry01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerGlucose oxidasePhysical and Theoretical Chemistrychemistry.chemical_classificationNicotinamidebiologyChemistryOrganic ChemistryPolymer021001 nanoscience & nanotechnology0104 chemical sciencesFerroceneElectrodebiology.protein0210 nano-technologyPlatinumJournal of Organometallic Chemistry
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Photochemistry of the H2O/CO System Revisited : The HXeOH···CO Complex in a Xenon Matrix

2017

We report on the complex of a noble-gas hydride HXeOH with carbon monoxide. This species is prepared via the annealing-induced H + Xe + OH···CO reaction in a xenon matrix, the OH···CO complexes being produced by VUV photolysis of the H2O···CO complexes. The H–Xe stretching mode of the HXeOH···CO complex absorbs at 1590.3 cm–1 and it is blue-shifted by 12.7 cm–1 from the H–Xe stretching band of HXeOH monomer. The observed blue shift indicates the stabilization of the H–Xe bond upon complexation, which is characteristic of complexes of noble-gas hydrides. The HXeOH···CO species is the first complex of a noble-gas hydride with carbon monoxide and the second observed complex of HXeOH. On the ba…

chemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencescarbon monoxidechemistry.chemical_compoundXenonmatricesNon-covalent interactionsMoleculegasesPhysical and Theoretical Chemistryta116chemistry.chemical_classificationphotochemistryHydrideIntermolecular forcePhotodissociation021001 nanoscience & nanotechnology0104 chemical sciencesMonomerchemistryH2O/CO system0210 nano-technologyCarbon monoxideJournal of Physical Chemistry C
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Selective Cobalt over Nickel separation using neat and confined ionic liquids

2020

International audience; Task Specific Ionic Liquids (TSILs) generated by association between tetraalkylammonium cations and coordinating anions such as dicyanamide (Dca-) and thiocyanate (SCN-) were used for the selective separation of Ni(II) over Co(II). SCN-based TSIL presents higher extraction efficiency than the Dca-based one towards Co(II) (E = 85.4 % vs 54.6 %) and Ni (II) (E = 22 % vs 0.5%) but lower separation factors (βCo/Ni = 21 vs 239). Interestingly, extraction of Co(II) and Ni(II) in Dca-based TSIL can be enhanced using salts with chaotropic anions such as NaNO3 (E > 90 % for Co(II) and E = 85% for Ni(II)). The use of NaCl allows, moreover, the efficient separation of both ions…

chemistry.chemical_element02 engineering and technology010501 environmental sciences01 natural sciencesMetalchemistry.chemical_compoundTSIL[CHIM.GENI]Chemical Sciences/Chemical engineeringRecyclabilityNickelChemical Engineering (miscellaneous)IonogelWaste Management and DisposalDicyanamide0105 earth and related environmental sciencesAqueous solutionThiocyanateProcess Chemistry and TechnologyExtraction (chemistry)Cobalt021001 nanoscience & nanotechnologyPollutionNickelchemistryvisual_artIonic liquidvisual_art.visual_art_medium0210 nano-technologyCobaltNuclear chemistry
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Comparative analysis of the remineralization potential of CPP–ACP with Fluoride, Tri-Calcium Phosphate and Nano Hydroxyapatite using SEM/EDX – An in …

2019

Background In recent years, the non-invasive management of non cavitated caries lesions using remineralization systems to repair the enamel have received more attention from the scientific community. Aim: To quantitatively evaluate the remineralization potential of Casein phosphopeptide-amorphous calcium phosphate-fluoride(CPP-ACPF), Tri-calcium phosphate(TCP) & Nano-hydroxyapatite(nHAP) using Scanning Electron Microscopy(SEM) and Energy dispersive X-ray Analysis(EDX). Material and Methods 40 enamel specimens were prepared, and immersed in demineralising solution at a pH of 4.4 for 96 hours at 37°C, to induce artificial carious lesions. Remineralization was carried out for a period of 30 da…

chemistry.chemical_element02 engineering and technologyCalcium03 medical and health scienceschemistry.chemical_compound0302 clinical medicinestomatognathic systemCaseinGeneral DentistryRemineralisationEnamel paintResearchPhosphorusTooth surface030206 dentistry:CIENCIAS MÉDICAS [UNESCO]021001 nanoscience & nanotechnologyPhosphateCommunity and Preventive Dentistrychemistryvisual_artUNESCO::CIENCIAS MÉDICASvisual_art.visual_art_medium0210 nano-technologyFluorideNuclear chemistryJournal of Clinical and Experimental Dentistry
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Selective Gold Recovery and Catalysis in a Highly Flexible Methionine-Decorated Metal–Organic Framework

2016

A novel chiral 3D bioMOF exhibiting functional channels with thio-alkyl chains derived from the natural amino acid l-methionine (1) has been rationally prepared. The well-known strong affinity of gold for sulfur derivatives, together with the extremely high flexibility of the thioether "arms" decorating the channels, account for a selective capture of gold(III) and gold(I) salts in the presence of other metal cations typically found in electronic wastes. The X-ray single-crystal structures of the different gold adsorbates Au(III)@1 and Au(I)@1 suggest that the selective metal capture occurs in a metal ion recognition process somehow mimicking what happens in biological systems and protein r…

chemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciencesBiochemistrySulfurCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryThioetherchemistryvisual_artvisual_art.visual_art_mediumOrganic chemistryMetal-organic framework0210 nano-technologyHybrid materialHydroalkoxylationJournal of the American Chemical Society
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The influence of Fe3+ doping on thermally induced crystallization and phase evolution of amorphous calcium phosphate

2021

The present study investigates thermally induced crystallization and phase evolution of amorphous calcium phosphate (ACP) partially substituted with Fe3+ ions (M/P = 1.5 : 1). It was demonstrated that the presence of Fe3+ ions radically changes the crystallization behavior of ACP and completely prevents the formation of α-tricalcium phosphate (α-TCP, Ca3(PO4)2), which is the first crystalline phase obtained from non-substituted ACP upon thermal treatment. Surprisingly, calcium deficient hydroxyapatite (CDHA) was obtained instead of α-TCP. Such unusual crystallization behavior was observed with a doping level as low as 0.1 mol% with respect to Ca ions. Moreover, it was shown that the presenc…

chemistry.chemical_element02 engineering and technologyGeneral ChemistryThermal treatmentCalcium010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsPhosphate01 natural sciences0104 chemical scienceslaw.inventionCrystallographychemistry.chemical_compoundchemistrylawPhase (matter)General Materials ScienceAmorphous calcium phosphateCrystallization0210 nano-technologyThermal analysisElectron paramagnetic resonanceCrystEngComm
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Electrochemical Characterization of Corrosion Products in Leaded Bronze Sculptures Considering Ohmic Drop Effects on Tafel Analysis

2015

[EN] The characterization of corrosion products in leaded bronze based on the voltammetry of immobilized particles methodology is described. Voltammetric data, supported by Fourier transform infra-red spectroscopy, field emission scanning electron microscopy-energy dispersive X-ray microanalysis (FESEM-EDX) and scanning electrochemical microscopy (SECM) allow the identification of copper and lead corrosion materials. The mutual influence of such products is modeled upon considering uncompensated ohmic drops in the Tafel analysis of the rising portion of the respective voltammetric signals for their electrochemical reduction.

chemistry.chemical_element02 engineering and technologyLeaded copper and bronzeengineering.material01 natural sciencesMicroanalysisUncompensated ohmic dropsAnalytical ChemistryCorrosionScanning electrochemical microscopyElectrochemistryBronzeTafel analysisVoltammetryOhmic contactTafel equationVoltammetry of immobilized particles010401 analytical chemistryMetallurgy021001 nanoscience & nanotechnologyCopper0104 chemical scienceschemistryPINTURAengineering0210 nano-technologySECM
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Towards oxalate-bridged iron(ii), cobalt(ii), nickel(ii) and zinc(ii) complexes through oxotris(oxalato)niobate(v): an open air non-oxidizing synthet…

2018

Four compounds with the formula [M2(dmphen)4(μ-C2O4)](ClO4)2·2dmso [M = Fe (1), Co (2) and Zn (4); dmphen = 2,9-dimethyl-1,10-phenanthroline] and [Ni2(dmphen)4(μ-C2O4)]3[NbO(C2O4)3]2·16H2O (3) have been synthesized using the tris(oxalato)oxoniobate(V) complex anion as the oxalate source, and their structures have been determined by single crystal X-ray diffraction. X-ray quality crystals of highly insoluble oxalate-bridged species were obtained by taking advantage of the slow release of oxalate by the tris(oxalato)oxoniobate(V) complex anion. The structures of 1–4 all contain oxalate-bridged dimetal(II) units with didentate dmphen molecules acting as end-cap ligands; electroneutrality is ac…

chemistry.chemical_element02 engineering and technologyZinc010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesOxalate0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundNickelPerchlorateCrystallographyPentagonal bipyramidal molecular geometrychemistryOctahedronMolecule0210 nano-technologyCobaltInorganic Chemistry Frontiers
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Maturation of a Key Resource – The Germanium-68/Gallium-68 Generator: Development and New Insights

2011

(68)Ge/(68)Ga radionuclide generators have been investigated for almost fifty years, since the cyclotron-independent availability of positron emitting (68)Ga via the (68)Ge/(68)Ga system had always attracted researches working in basic nuclear chemistry as well as radiopharmaceutical chemistry. However, it took decades and generations of research (and researchers) to finally reach a level of (68)Ge/(68)Ga radionuclide generator designs adequate to the modern requirements of radiometal labelling chemistry. Nevertheless, most of the existing commercial generator systems address aspects of (68)Ge breakthrough and safe synthesis of (68)Ga radiopharmaceuticals by adopting eluate post-processing …

chemistry.chemical_elementGallium RadioisotopesGermaniumNanotechnologyChemical FractionationRadiology Nuclear Medicine and imagingCation Exchange ResinsProcess engineeringAnion Exchange ResinsEdetic AcidChelating AgentsRadioisotopesPharmacologyGenerator (computer programming)Gallium-68 generatorGermaniumbusiness.industryRadionuclide GeneratorsSolid Phase ExtractionChemical fractionationRadioactivitychemistryPositron-Emission TomographyRadiopharmaceuticalsRadionuclide GeneratorbusinessCurrent Radiopharmaceuticals
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Atrane complexes chemistry as a tool for obtaining trimodal UVM-7-like porous silica

2018

[EN] The use of atrane complexes as hydrolytic precursors enables the homogeneous incorporation of manganese (25Si/Mn48) throughout the porous walls of the nanoparticles of a surfactant-templated bimodal mesoporous silica (UVM-7). The subsequent leaching of the manganese nanodomains allows adding controlled microporosity to the host silica framework. The resulting final silica material presents three pore systems structured at different length scales: interparticle textural-type macroporosity (ca. 43.2nm), ordered intraparticle mesoporosity (ca. 2.63nm; after template removal), and well-dispersed microporosity (< 2nm; as consequence of the lixiviation of the Mn-rich domains). The good dispe…

chemistry.chemical_elementNanoparticle02 engineering and technologyManganeseMesoporous010402 general chemistry01 natural scienceschemistry.chemical_compoundAtrane complexesMaterials ChemistryPhysical and Theoretical ChemistryPorosityChemistryQUIMICA INORGANICASilicaMicroporous materialMesoporous silica021001 nanoscience & nanotechnology0104 chemical sciencesAtraneChemical engineeringEtchingMicroporousLeaching (metallurgy)0210 nano-technologyMesoporous material
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