Search results for "SCAD"

showing 10 items of 348 documents

On the staking of miniaturized air-breathing microbial fuel cells

2018

Abstract This work focuses on the scale-up of the MFCs by miniaturization and multiplication strategy. Performances of five stacks containing 1, 2, 5, 8 and 16 MFCs were compared. Each stack was evaluated under individual, parallel and series electrical connection as well as for cascade or individual hydraulic connection. Cascade feeding mode with a tank per stack favours the COD removal when the number of MFCs in the stack increases. However, despite operating without COD limitations, the energy production was disadvantaged. By changing the feeding system of a tank per stack into an individual tank per MFC, the performance of the whole stack enhances considerably. Stacking in series can in…

Microbial fuel cellMaterials scienceMicrobial fuel cellCombustiblesStackingStack02 engineering and technology010501 environmental sciencesManagement Monitoring Policy and Law01 natural sciencesStack (abstract data type)MiniaturizationMultiplicationProcess engineering0105 earth and related environmental sciencesMiniaturizationbusiness.industryMechanical EngineeringBuilding and Construction021001 nanoscience & nanotechnologyElectrical connectionPower (physics)ElectroquímicaGeneral EnergyCascadeCascade0210 nano-technologybusinessVoltage
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Estimation of the mean crystal size and the moments of the crystal size distribution in batch crystallization processes

2016

International audience; A cascade high gain observer is designed to estimate the first four leading moments of the crystal size distribution (CSD) and the mean crystal size in batch crystallization processes. The proposed observer is based on a well-known transformation of the partial differential equation describing the CSD to a set of ordinary differential equations (the method of moments). Due to numerical difficulties resulting from the important differences in the magnitudes of the moments, a set of new variables is computed to allow a good estimation of the moments and thus the mean crystal size. In this work, only solute concentration and crystallizer temperature are used to estimate…

Model-Predictive ControlIdentification[ INFO ] Computer Science [cs]Observer (quantum physics)population balance equations02 engineering and technologyMethod of moments (statistics)high gain observer[SPI.AUTO]Engineering Sciences [physics]/Automaticlaw.inventionCrystalCrystallization processes020401 chemical engineeringFbrmControl theorylawBeam Reflectance Measurement[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineering[INFO]Computer Science [cs]L-Glutamic Acid0204 chemical engineeringCrystallizationComputingMilieux_MISCELLANEOUSMathematicsParticle-SizePartial differential equationmethod of momentsMathematical analysisShape021001 nanoscience & nanotechnologyImage-Analysiscrystal size distributionTransformation (function)CascadeOrdinary differential equation0210 nano-technologyProduct
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Tandem Nucleophilic Addition−Intramolecular Aza-Michael Reaction: Facile Synthesis of Chiral Fluorinated Isoindolines

2010

A highly stereoselective synthesis of fluorinated 1,3-disubstituted isoindolines is described. To this end, a tandem reaction consisting of a diastereoselective addition of fluorinated nucleophiles to Ellman's N-(tert-butanesulfinyl)imines followed by an intramolecular aza-Michael reaction has been developed. This strategy allows for the construction of isoindolines bearing several degrees of fluorination (mono-, di-, or trifluoromethyl as well as heavier fluorinated groups). In the majority of all cases, the products are formed as single isomers.

Models MolecularAza CompoundsIndolesTrifluoromethylNucleophilic additionHalogenationMolecular StructureTandemHydrolysisOrganic ChemistryStereoisomerismIsoindolesBiochemistryMedicinal chemistrychemistry.chemical_compoundCascade reactionchemistryNucleophileIntramolecular forceMichael reactionOrganic chemistryStereoselectivityPhysical and Theoretical ChemistryOrganic Letters
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Amidrazone Complexes from a Cascade Platinum(II)-Mediated Reaction between Amidoximes and Dialkylcyanamides

2013

The aryl amidoximes R'C6H4C(NH2)═NOH (R' = Me, 2a; H, 2b; CN, 2c; NO2, 2d) react with the dialkylcyanamide platinum(II) complexes trans-[PtCl2(NCNAlk2)2] (Alk2 = Me2, 1a; C5H10, 1b) in a 1:1 molar ratio in CHCl3 to form chelated mono-addition products [3a-h]Cl, viz. [PtCl(NCNAlk2){NH═C(NR2)ON═C(C6H4R')NH2}]Cl (Alk2 = Me2; R' = Me, a; H, b; CN, c; NO2, d; Alk2 = C5H10; R' = Me, e; H, f; CN, g; NO2, h). In the solution, these species spontaneously transform to the amidrazone complexes [PtCl2{NH═C(NR2)NC(C6H4R')NNH2}] (7a-h; 36-47%); this conversion proceeds more selectively (49-60% after column chromatography) in the presence of the base (PhCH2)3N. The observed reactivity pattern is specific …

Models MolecularC5H10Molecular StructureOrganoplatinum CompoundsArylchemistry.chemical_elementCrystallography X-RayAmidesMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryCascadeOximesOrganic chemistryPhysical and Theoretical ChemistryPlatinumta116Inorganic Chemistry
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Stereoselective Synthesis of P-Chirogenic Dibenzophosphole-Boranes via Aryne Intermediates

2012

A new aryne-mediated tandem cross-coupling/P-cyclization sequence starting from tertiary phosphine-boranes and 1,2-dibromobenzenes is reported. P-chirogenic dibenzophospholes become accessible in a regio-, chemo-, and diastereoselective way.

Models MolecularMolecular StructurePhosphines010405 organic chemistryStereochemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryCross reactionsRegioselectivityStereoisomerismBoranes010402 general chemistry01 natural sciencesAryneChemical synthesis0104 chemical sciences3. Good healthCascade reactionCyclizationAlkynesStereoselectivityChemoselectivityBoranes
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Multifaceted Palladium Catalysts Towards the Tandem Diboration-Arylation Reactions of Alkenes

2008

Novel Pd(2) (6+) compounds have been synthesized in high yield. These compounds and their Pd(2) (4+) counterparts as synthetic precursors mediate the diboration of vinylarenes and aliphatic 1-alkenes, and under mild and basic reaction conditions they produce a variety of 1,2-diboronate esters with excellent conversions and chemoselectivities. The presence of bis(catecholato)diboron (B(2)cat(2)) favours the reduction of Pd(III) to Pd(II), while the catalytic precursor of Pd(II) is transformed into Pd(0)-nanoparticles. An "in situ" catalytic tandem reaction has been designed to transform the diboronate intermediates into the monoarylated product, which after oxidative workup, provides the car…

Models MolecularTime Factorschemistry.chemical_elementStereoisomerismAlkenesCrystallography X-RayCatalysisAdductCatalysisCascade reactionOrganometallic CompoundsOrganic chemistryParticle SizeChemoselectivitychemistry.chemical_classificationMolecular StructureChemistryAlkeneOrganic ChemistryStereoisomerismGeneral ChemistryBoronic AcidsCombinatorial chemistryAlcoholsYield (chemistry)PalladiumPalladiumChemistry - A European Journal
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A Molecular Electron Density Theory Study of the Synthesis of Spirobipyrazolines through the Domino Reaction of Nitrilimines with Allenoates

2019

The reaction of diphenyl nitrilimine (NI) with methyl 1-methyl-allenoate yielding a spirobipyrazoline has been studied within molecular electron density theory (MEDT) at the MPWB1K/6-311G(d) computational level in dichloromethane. This reaction is a domino process that comprises two consecutive 32CA reactions with the formation of a pyrazoline intermediate. Analysis of the relative Gibbs free energies indicates that both 32CA reactions are highly regioselective, the first one being also completely chemoselective, in agreement with the experimental outcomes. The geometries of the TSs indicate that they are associated to asynchronous bond formation processes in which the shorter distance invo…

Models Molecular[3+2] cycloaddition reactionsMolecular ConformationPharmaceutical SciencePyrazoline010402 general chemistrynitrilimines7. Clean energy01 natural sciencesArticleallenoatesAnalytical Chemistrylcsh:QD241-441symbols.namesakechemistry.chemical_compoundlcsh:Organic chemistryNucleophileCascade reactionComputational chemistryDrug DiscoverySpiro CompoundsPhysical and Theoretical ChemistryDichloromethaneCycloaddition ReactionMolecular Structure010405 organic chemistryChemistryNitrilimineOrganic Chemistrydomino reactionsmolecular electron density theoryRegioselectivityspirobipyrazolinesModels Theoretical0104 chemical sciencesGibbs free energyChemistry (miscellaneous)ElectrophilesymbolsMolecular MedicineIminesmolecular mechanismMolecules
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Asymmetric Synthesis of Spirocyclic β-Lactams through Copper-Catalyzed Kinugasa/Michael Domino Reactions

2018

The first copper-catalyzed highly chemo-, regio-, diastereo-, and enantioselective Kinugasa/Michael domino reaction for the desymmetrization of prochiral cyclohexadienones is described. In the presence of a chiral copper catalyst, alkyne-tethered cyclohexadienones couple with nitrones to generate the chiral spirocyclic lactams with excellent stereoselectivity (up to 97 % ee, >20:1 dr). The new method provides direct access to versatile highly functionalized spirocyclic β-lactams possessing four contiguous stereocenters, including one quaternary and one tetra-substituted stereocenter.

Molecular Structure010405 organic chemistryStereochemistryChemistryasymmetric synthesisEnantioselective synthesisGeneral MedicineGeneral Chemistrybeta-Lactams010402 general chemistry01 natural sciencesDesymmetrizationCatalysisDomino0104 chemical sciencesCatalysisStereocenterCascade reactionAlkynesβ lactamsStereoselectivityta116CopperAngewandte Chemie International Edition
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Experimental and DFT Studies on Competitive Heterocyclic Rearrangements. 3. A Cascade Isoxazole−1,2,4-Oxadiazole−Oxazole Rearrangement

2008

The thermal rearrangements of 3-acylamino-5-methylisoxazoles 1 have been investigated under basic and neutral conditions and interpreted with the support of computational data. The density functional theory (DFT) study on the competitive routes available for the base-catalyzed thermal rearrangement of isoxazoles 1 showed that the Boulton-Katritzky (BK) rearrangement, producing the less stable 3-acetonyl-1,2,4-oxadiazoles 5, is a much more favored process than either the migration-nucleophilic attack-cyclization (MNAC) or the ring contraction-ring expansion (RCRE). In turn, an increase in reaction temperature will promote the MNAC of oxadiazoles 5, producing the more stable 2-acylaminooxazol…

Molecular StructureStereochemistryOrganic ChemistryTemperatureOxadiazoleStereoisomerismRing (chemistry)Turn (biochemistry)chemistry.chemical_compoundModels ChemicalchemistryCyclizationComputational chemistryCascadeComputer SimulationDensity functional theoryIsoxazoleOxazolesOxazoleCope rearrangementThe Journal of Organic Chemistry
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Low-energy primary knock on atom damage distributions near MeV proton beams focused to nanometre dimensions

2007

Abstract In this preliminary study, the spatial extent of the defects introduced in Si by a normally incident 1 MeV H + nanobeam was investigated using a hybrid approach. First, the standard SRIM code was employed to calculate the angular and energy distributions of Primary Knock-on Atoms (PKA) using the Binary Collision Approximation (BCA). The long mean free path and the kinematics of scattering in a screened Coulomb potential resulted in an anisotropic PKA distribution that was mainly directed perpendicular to the primary ion trajectories. The PKA energy E dependence was close to 1/ E n with 1.5  n The results revealed that the low energy PKA’s resulted in localised damaged regions with …

Nuclear and High Energy PhysicsProtonChemistryMean free pathIon trackAtomCollision cascadeElectric potentialAtomic physicsBinary collision approximationInstrumentationIonNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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