Search results for "Calcination"

showing 10 items of 112 documents

Modulation of folic acid bioaccessibility by encapsulation in pH-responsive gated mesoporous silica particles

2015

[EN] A study on the controlled release of folic acid (FA) from pH-responsive gated mesoporous silica particles (MSP) is reported. The MCM-41 support was synthesized using tetraethyl orthosilicate (TEOS) as hydrolytic inorganic precursor and the surfactant hexadecyltrimethylammonium bromide (CTAB) as porogen species. Calcination of the mesostructured phase resulted in the starting solid. This solid was loaded with FA to obtain the initial support S0. Moreover, this FA-loaded material was further functionalized with 3-[2-(2-aminoethylamino)ethylamino]propyltrimethoxysilane (N3) in order to obtain the gated polyamine-functionalised material S1. Solids S0 and S1 were characterized using standar…

INGENIERIA DE LA CONSTRUCCIONFolic acidTECNOLOGIA DE ALIMENTOSBioaccessibilityMesoporous silica particleslaw.inventionchemistry.chemical_compoundHydrolysisQUIMICA ORGANICAPulmonary surfactantlawControlled releaseGeneral Materials ScienceCalcinationLoading optimizationChromatographyChemistryQUIMICA INORGANICAGeneral ChemistryMesoporous silicaCondensed Matter PhysicsControlled releaseTetraethyl orthosilicateMechanics of MaterialsSurface modificationMesoporous materialNuclear chemistry
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Au deposited on CeO2 prepared by a nanocasting route: A high activity catalyst for CO oxidation

2014

Abstract A set of catalysts comprised of gold on different CeO 2 supports has been prepared by a nanocasting route and characterized by several physicochemical techniques. These catalysts have been tested for CO oxidation and show outstanding catalytic activity. Higher calcination temperatures of the hard template, producing a poorly ordered silica template, have led to a higher amount of oxygen vacancies on the surface of CeO 2 . The presence of surface oxygen defects in the support combined with the deposition of Au nanoparticles ( ca. 3 nm) homogeneously dispersed on the CeO 2 support may explain the excellent behaviour for low temperature CO oxidation. Surprisingly, it has been observed…

Inorganic chemistryNanoparticleCatalytic combustionCatalysisCatalysislaw.inventionchemistry.chemical_compoundchemistryColloidal goldlawOxidation stateCalcinationPhysical and Theoretical ChemistryDispersion (chemistry)Carbon monoxideJournal of Catalysis
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Physicochemical Characterization of Isomorphously Substituted FeZSM-5 during Activation

2002

Physicochemical characteristics of isomorphously substituted FeZSM-5 both after preparation and after activation have been determined by gas (Ar and N2) physisorption, 27Al and 29Si magic-angle spinning–nuclear magnetic resonance, NH3 temperature-programmed desorption, transmission electron microscopy, H2 temperature-programmed reduction (TPR), 57Fe Mossbauer spectroscopy, and voltammetric response techniques. The activation of as-synthesized FeZSM-5 comprises calcination at 823 K and a subsequent steam treatment (300 mbar of H2O in N2) at 873 K. Calcination leads to complete removal of the template. During this process a significant fraction of iron is dislodged to extraframework positions…

Inorganic chemistryOxideHeterogeneous catalysisCatalysisCatalysislaw.inventionchemistry.chemical_compoundchemistrylawDesorptionMössbauer spectroscopyCalcinationPhysical and Theoretical ChemistryZeoliteIron oxide nanoparticlesJournal of Catalysis
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Reactive adsorption of thiophene on Ni/ZnO: role of hydrogen pretreatment and nature of the rate determining step.

2008

Abstract Reactive adsorption of thiophene on reduced and unreduced NiO/ZnO adsorbents was studied by thermal gravimetric analysis and by sulfidation in a fixed bed reactor at 330–375 °C and 10–40 mbar of thiophene in hydrogen. The adsorbents (12 wt% Ni) were prepared by co-precipitation of corresponding nitrates with sodium carbonate followed by calcination at 400 °C. We have found that such solids can react with thiophene without any prior reduction. Metallic Ni, indispensable for thiophene decomposition, is formed in this case in situ upon the contact with thiophene/H 2 reaction mixture. The reduction of NiO/ZnO in H 2 (360 °C, 6 h) results in the formation of Ni–Zn alloyed particles (as …

Inorganic chemistrySulfidation02 engineering and technologyActivation energy010402 general chemistry01 natural sciencesCatalysislaw.inventionCatalysis[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Reaction ratechemistry.chemical_compoundAdsorptionlawThiopheneCalcinationComputingMilieux_MISCELLANEOUSGeneral Environmental ScienceProcess Chemistry and Technology021001 nanoscience & nanotechnologyRate-determining step0104 chemical sciences[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]chemistry13. Climate action[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technology
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Effect of Gold on the HDS Activity of Supported Palladium Catalysts

2002

Abstract The effect of gold on palladium catalysts supported on amorphous aluminosilicate was investigated in the hydrodesulfurization of thiophene. A series of bimetallic AuxPdy catalysts was prepared by the slow deposition–precipitation method with decomposition of urea. The structural and surface properties of the samples were analyzed by X-ray diffraction and X-ray photoelectron spectroscopy techniques at different stages of the catalyst life. After calcination at 673 K, gold-enriched solid solutions of approximately Au90Pd10 and Au80Pd20 composition were formed for all samples of different Au/Pd ratios, along with free palladium phases. Au80Pd20 was the prevailing phase. Hydrogen treat…

Inorganic chemistrychemistry.chemical_elementHeterogeneous catalysisCatalysislaw.inventionCatalysisMetalchemistry.chemical_compoundchemistrylawvisual_artThiophenevisual_art.visual_art_mediumCalcinationPhysical and Theoretical ChemistryBimetallic stripHydrodesulfurizationPalladiumJournal of Catalysis
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Hybrid magnetic materials formed by ferritin intercalated into a layered double hydroxide

2008

A hybrid magnetic material formed by ferritin intercalated into a layered double hydroxide (LDH) of Mg and Al (Mg/Al molar ratio 2) is prepared and characterized through powder X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR) spectroscopy, electron probe microanalysis (EPMA) and high resolution transmission electron microscopy (HRTEM). One observes an enhancement in the thermal stability of the ferritin molecules when they are inserted in the layered material. Magnetic measurements of the hybrid material exhibit the typical superparamagnetic behaviour of the ferritin molecule. On the other hand, the intercalation of ferritin into the LDH guarante…

Intercalation (chemistry)Analytical chemistryGeneral ChemistryCondensed Matter PhysicsFourier transform spectroscopylaw.inventionchemistry.chemical_compoundchemistrylawHydroxideMagnetic nanoparticlesGeneral Materials ScienceCalcinationHigh-resolution transmission electron microscopyHybrid materialSuperparamagnetismSolid State Sciences
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Electrochemical characterization of iron sites in ex-framework FeZSM-5

2002

Abstract The electrochemical response of FeZSM-5 prepared by an ex-framework method has been studied using Paraloid B72 polymer film electrodes immersed in aqueous media using H2SO4, HCl, Na2EDTA and NaCl electrolytes. The ex-framework method comprises the hydrothermal synthesis of isomorphously substituted FeZSM-5, followed by calcination at 823 K and subsequent steam treatment (300 mbar H2O in N2) at 873 K. During this process iron is extracted to extra-framework positions. Also partial dealumination of the zeolite framework takes place. Characteristic voltammetric responses in the +1.0 to −0.6 V versus SCE potential range have been recorded and were used to characterize the iron species …

Ion exchangeChemistryGeneral Chemical EngineeringInorganic chemistryIron oxideElectrochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawElectrochemistryHydrothermal synthesisCalcinationCyclic voltammetryZeoliteDissolutionJournal of Electroanalytical Chemistry
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Precipitation and Calcination of High-Capacity LiNiO2 Cathode Material for Lithium-Ion Batteries

2020

This article presents the electrochemical results that can be achieved for pure LiNiO2 cathode material prepared with a simple, low-cost, and efficient process. The results clarify the roles of the process parameters, precipitation temperature, and lithiation temperature in the performance of high-quality LiNiO2 cathode material. Ni(OH)2 with a spherical morphology was precipitated at different temperatures and mixed with LiOH to synthesize the LiNiO2 cathode material. The LiNiO2 calcination temperature was optimized to achieve a high initial discharge capacity of 231.7 mAh/g (0.1 C/2.6 V) with a first cycle efficiency of 91.3% and retaining a capacity of 135 mAh/g after 400 cycles. These a…

LNOcathodeMaterials scienceelektroditlitiumioniakutchemistry.chemical_elementlithium-ion battery02 engineering and technology010402 general chemistryElectrochemistrylcsh:Technology01 natural sciencesLithium-ion batteryIonlaw.inventionlcsh:Chemistrylithium nickel oxideCathode materiallawGeneral Materials ScienceCalcinationlcsh:QH301-705.5InstrumentationFluid Flow and Transfer Processeslcsh:TPrecipitation (chemistry)Process Chemistry and TechnologyGeneral Engineeringmateriaalit021001 nanoscience & nanotechnologysähkökemialcsh:QC1-999Cathode0104 chemical sciencesComputer Science Applicationslitiumlcsh:Biology (General)lcsh:QD1-999Chemical engineeringchemistrylcsh:TA1-2040oksiditLithiumnikkelilcsh:Engineering (General). Civil engineering (General)0210 nano-technologylcsh:PhysicsApplied Sciences
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Not always what closes best opens better: mesoporous nanoparticles capped with organic gates

2019

ABSTRACT Four types of calcined MCM-41 silica nanoparticles, loaded with dyes and capped with different gating ensembles are prepared and characterized. N1 and N2 nanoparticles are loaded with rhodamine 6G and capped with bulky poly(ethylene glycol) derivatives bearing ester groups (1 and 2). N3-N4 nanoparticles are loaded with sulforhodamine B and capped with self-immolative derivatives bearing ester moieties. In the absence of esterase enzyme negligible cargo release from N1, N3 and N4 nanoparticles is observed whereas a remarkable release for N2 is obtained most likely due to the formation of an irregular coating on the outer surface of the nanoparticles. In contrast, a marked delivery i…

Materials science102 Porous / Nanoporous / Nanostructured materialslcsh:BiotechnologyNanoparticle02 engineering and technologyGating010402 general chemistryEngineering and Structural Materials01 natural scienceslaw.inventionSilica nanoparticlesRhodamine 6Gchemistry.chemical_compoundlaw10 Engineering and Structural materialslcsh:TP248.13-248.65lcsh:TA401-492General Materials ScienceCalcinationgated nanodevices021001 nanoscience & nanotechnologyesterase controlled release0104 chemical sciencesChemical engineeringchemistrylcsh:Materials of engineering and construction. Mechanics of materials0210 nano-technologyMesoporous materialmesoporous nanoparticles
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Synthesis of YAG nanopowder by the co-precipitation method: Influence of pH and study of the reaction mechanisms

2012

International audience; YAG nanopowders with an average grain size of 30 nm have been successfully synthesized by the co-precipitation method using nitrates with precipitant of ammonium hydrogen carbonate. The influence of precipitation conditions such as pH, aging time and calcination temperature on the formation of secondary phases has been studied. The accurate control of pH value at every stage of precipitation process is crucial to avoid the presence of YAM (Yttrium Aluminium Monoclinic, Y4Al2O9) and yttrium oxide (Y2O3) after calcination. The reaction mechanisms have been investigated using different techniques such as infrared spectroscopy, x-ray diffraction and thermal analyses. The…

Materials scienceCoprecipitationInorganic chemistryOxideTRANSPARENT CERAMICSFABRICATIONchemistry.chemical_element02 engineering and technology01 natural scienceslaw.inventionInorganic Chemistrychemistry.chemical_compoundlawAluminiumYTTRIUM-ALUMINUM-GARNET0103 physical sciencesMaterials ChemistryNANO-SIZED POWDERCalcinationPhysical and Theoretical ChemistryPerovskite (structure)010302 applied physicsPRECURSORSPrecipitation (chemistry)Yttrium021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectronic Optical and Magnetic MaterialschemistryChemical engineeringPRECIPITATIONCeramics and CompositesLASER0210 nano-technologyMonoclinic crystal system
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