Search results for "Colloid"

showing 10 items of 1288 documents

Monte Carlo simulations of the solid-liquid transition in hard spheres and colloid-polymer mixtures

2010

Monte Carlo simulations at constant pressure are performed to study coexistence and interfacial properties of the liquid-solid transition in hard spheres and in colloid-polymer mixtures. The latter system is described as a one-component Asakura-Oosawa (AO) model where the polymer's degrees of freedom are incorporated via an attractive part in the effective potential for the colloid-colloid interactions. For the considered AO model, the polymer reservoir packing fraction is eta_p^r=0.1 and the colloid-polymer size ratio is q=sigma_p/\sigma=0.15 (with sigma_p and sigma the diameter of polymers and colloids, respectively). Inhomogeneous solid-liquid systems are prepared by placing the solid fc…

ANISOTROPIC SURFACE-TENSIONMaterials scienceMonte Carlo methodDegrees of freedom (physics and chemistry)General Physics and AstronomyThermodynamicsCondensed Matter - Soft Condensed MatterCAPILLARY WAVESAtomic packing factorCOMPUTER-SIMULATIONVAPOR INTERFACE3-DIMENSIONAL ISING-MODELColloidsymbols.namesakePhase (matter)Physical and Theoretical ChemistryCOEXISTING PHASESchemistry.chemical_classificationCondensed Matter - Materials ScienceINTERFACIAL FREE-ENERGYPROFILESHard spheresPolymerCondensed Matter::Soft Condensed MatterchemistryCRYSTAL-MELT INTERFACESBoltzmann constantsymbolsCRYSTALLIZATIONThe Journal of Chemical Physics
researchProduct

Stabilized Naked Sub-nanometric Cu Clusters within a Polymeric Film Catalyze C-N, C-C, C-O, C-S, and C-P Bond-Forming Reactions

2015

[EN] Sub-nanometric Cu clusters formed by endogenous reduction of Cu salts and Cu nanoparticles are active and selective catalysts for C−N, C−C, C−O, C−S, and C−P bond-forming reactions. Sub-nanometric Cu clusters have also been generated within a polymeric film and stored with full stability for months. In this way, they are ready to be used on demand and maintain high activity (TONs up to 104 ) and selectivity for the above reactions. A potential mechanism for the formation of the sub-nanometric clusters and their electronic nature is presented.

ARYL HALIDESTECNOLOGIA DE ALIMENTOSDIAMINE LIGANDSULLMANNHeterogeneous catalysisBiochemistryCatalysisCoupling reactionCatalysisMECHANISMSColloid and Surface ChemistryQUIMICA ORGANICAOn demandPolymer chemistryOxidationHigh activityOrganic chemistryPotential mechanismTEMPERATURECu nanoparticlesChemistryGeneral ChemistryHETEROGENEOUS CATALYSISCROSS-COUPLING REACTIONSGOLD CLUSTERSSelectivityCOPPER CLUSTERS
researchProduct

Coupling between bulk- and surface chemistry in suspensions of charged colloids

2013

The ionic composition and pair correlations in fluid phases of realistically salt-free charged colloidal sphere suspensions are calculated in the primitive model. We obtain the number densities of all ionic species in suspension, including low-molecular weight microions, and colloidal macroions with acidic surface groups, from a self-consistent solution of a coupled physicochemical set of nonlinear algebraic equations and non-mean-field liquid integral equations. Here, we study suspensions of colloidal spheres with sulfonate or silanol surface groups, suspended in demineralized water that is saturated with carbon dioxide under standard atmosphere. The only input required for our theoretical…

Ab initioFOS: Physical sciencesGeneral Physics and AstronomyIonic bondingCondensed Matter - Soft Condensed MatterIonSuspension (chemistry)Condensed Matter::Soft Condensed MatterSilanolchemistry.chemical_compoundColloidSulfonatechemistryChemical physicsSoft Condensed Matter (cond-mat.soft)SPHERESPhysical and Theoretical ChemistryThe Journal of Chemical Physics
researchProduct

The Coordination of Uranyl in Water: A Combined Quantum Chemical and Molecular Simulation Study

2005

The coordination environment of uranyl in water has been studied using a combined quantum mechanical and molecular dynamics approach. Multiconfigurational wave function calculations have been performed to generate pair potentials between uranyl and water. The quantum chemically determined energies have been used to fit parameters in a polarizable force field with an added charge transfer term. Molecular dynamics simulations have been performed for the uranyl ion and up to 400 water molecules. The results show a uranyl ion with five water molecules coordinated in the equatorial plane. The U-O(H(2)O) distance is 2.40 A, which is close to the experimental estimates. A second coordination shell…

Ab initioMolecular simulationBiochemistryCatalysisIonMolecular dynamicschemistry.chemical_compoundColloid and Surface ChemistryAb initio quantum chemistry methodsComputational chemistryComputer SimulationPhysics::Chemical PhysicsQuantum chemicalHydrogen bondSolvationWaterGeneral ChemistryGeneral MedicineUranylSolvation shellchemistryModels ChemicalChemical physicsddc:540Quantum TheoryUranium
researchProduct

Synthesis and Physical Stability of Novel Au-Ag@SiO<SUB>2</SUB> Alloy Nanoparticles

2012

The present study describes the synthesis of nanoparticles of silver-gold alloys and with their electrokinetic and spectroscopic characterisation. The synthesis was made in two steps. In the first step silver nanoparticles coated with silica (Ag@SiO2) were synthesised using a novel method assisted by laser ablation. The second step consisted on the introduction of KAuCl4 in the colloidal solution of Ag@ SiO2 nanoparticles in order to obtain silica-coated silver-gold alloy nanoparticles. The changes of colour and mean diameter of Ag@SiO2 nanoparticles caused by the introduction of the gold salt were found dependent on its concentration. Upon increasing (KAuCl4) the diameter of nanoparticles …

AbsorbanceColloidMaterials scienceAlloyAnalytical chemistryengineeringNanoparticleDLVO theoryInteraction energyengineering.materialSurface plasmon resonanceSilver nanoparticleNanoscience and Nanotechnology
researchProduct

[Pt2Cu34(PET)22Cl4]2–: An Atomically Precise, 10-Electron PtCu Bimetal Nanocluster with a Direct Pt–Pt Bond

2021

Heteroatom-doped metal nanoclusters (NCs) are highly desirable to gain fundamental insights into the effect of doping on the electronic structure and catalytic properties. Unfortunately, their controlled synthesis is highly challenging when the metal atomic sizes are largely different (e.g., Cu and Pt). Here, we design a metal-exchange strategy that enables simultaneous doping and resizing of NCs. Specifically, [Pt2Cu34(PET)22Cl4]2- NC, the first example of a Pt-doped Cu NC, is synthesized by utilizing the unique reactivity of [Cu32(PET)24Cl2H8]2- NC with Pt4+ ions. The single-crystal X-ray structure reveals that two directly bonded Pt atoms occupy the two centers of an unusually interpenet…

Absorption spectroscopy010405 organic chemistrySuperatomDopingGeneral ChemistryElectronic structure010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesNanoclustersSilanolchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryMoleculeDensity functional theoryJournal of the American Chemical Society
researchProduct

Regioselective Hydrogenation of a 60-Carbon Nanographene Molecule toward a Circumbiphenyl Core.

2019

Regioselective peripheral hydrogenation of a nanographene molecule with 60 contiguous sp2 carbons provides unprecedented access to peralkylated circumbiphenyl (1). Conversion to the circumbiphenyl core structure was unambiguously validated by MALDI-TOF mass spectrometry, NMR, FT-IR, and Raman spectroscopy. UV–vis absorption spectra and DFT calculations demonstrated the significant change of the optoelectronic properties upon peripheral hydrogenation. Stimulated emission from 1, observed via ultrafast transient absorption measurements, indicates potential as an optical gain material.

Absorption spectroscopyChemistryCommunicationChemistry (all)RegioselectivityGeneral Chemistry010402 general chemistryMass spectrometryPhotochemistryCatalysis; Chemistry (all); Biochemistry; Colloid and Surface Chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCatalysissymbols.namesakeColloid and Surface ChemistryUltrafast laser spectroscopysymbolsMoleculeStimulated emissionRaman spectroscopyJournal of the American Chemical Society
researchProduct

[Cu32(PET)24H8Cl2](PPh4)2: A Copper Hydride Nanocluster with a Bisquare Antiprismatic Core

2020

Atomically precise coinage metal (Au, Ag, and Cu) nanoclusters (NCs) have been the subject of immense interest for their intriguing structural, photophysical, and catalytic properties. However, the synthesis of Cu NCs is highly challenging because of low reduction potential and high reactivity of copper, demonstrating the need for new synthetic methods using appropriate ligand combinations. By designing a diamine-assisted synthetic strategy, here we report the synthesis and total structure characterization of a box-like dianionic Cu NC [Cu32(PET)24H8Cl2](PPh4)2 coprotected by 2-phenylethanethiolate (PET), hydride, and chloride ligands. Its crystal structure comprises a rare bisquare antipri…

Absorption spectroscopyHydrideChemistryLigandGeneral ChemistryElectronic structureCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesNanoclustersCrystallographychemistry.chemical_compoundColloid and Surface ChemistryCopper hydrideDensity functional theoryJournal of the American Chemical Society
researchProduct

Experimental and robust modeling approach for lead(II) uptake by alginate gel beads: influence of the ionic strength and medium composition.

2014

Abstract Systematic kinetic and equilibrium studies on the lead ions removal ability by Ca-alginate gel beads have been performed by varying several internal parameters, namely, number of gel beads, nature and composition of the ionic medium and pH, which allowed us to model a wastewater in order to closely reproduce the composition of a real sample. Moreover, the effects brought about the different ionic species present in the reacting medium have been evaluated. Differential Pulse Anodic Stripping Voltammetry (DP-ASV), has been systematically used to perform kinetic and equilibrium measurements over continuous time in a wide range of concentration. Kinetic and equilibrium data have been q…

Accuracy and precisionChemistryAnalytical chemistryIonic bondingKinetic energySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonBiomaterialsAnodic stripping voltammetryColloid and Surface ChemistryIonic strengthAlginate gel beads Robust statistics Metal adsorption Wastewater treatment Ionic strength Differential Pulse Anodic Stripping Voltammetry Adsorption isotherms Adsorption kinetics Lead Heavy metalmedicineComposition (visual arts)Settore CHIM/01 - Chimica AnaliticaSwellingmedicine.symptomJournal of colloid and interface science
researchProduct

Measuring single small molecule binding via rupture forces of a split aptamer.

2011

The rupture force of a split (bipartite) aptamer that forms binding pockets for adenosine monophosphate (AMP) was measured by atomic force spectroscopy. Changes in the rupture force were observed in the presence of AMP, while this effect was absent when mutant aptamers or inosine were used. Thus, changes in the rupture force were a direct consequence of specific binding of AMP to the split aptamer. The split aptamer concept allowed the detection of nonlabeled AMP and enabled us to determine the dissociation constant on a single-molecule level.

Adenosine monophosphateChemistryAptamerForce spectroscopyGeneral ChemistryPlasma protein bindingAptamers NucleotideMicroscopy Atomic ForceBiochemistryCatalysisAdenosine MonophosphateDissociation constantCrystallographychemistry.chemical_compoundColloid and Surface ChemistrymedicineDirect consequenceSmall molecule bindingInosinemedicine.drugProtein BindingJournal of the American Chemical Society
researchProduct