Search results for "Colloid"

showing 10 items of 1288 documents

Controlled UV-C light-induced fusion of thiol-passivated gold nanoparticles.

2011

Thiol-passivated gold nanoparticles (AuNPs) of a relatively small size, either decorated with chromophoric groups, such as a phthalimide (Au@PH) and benzophenone (Au@BP), or capped with octadecanethiol (Au@ODCN) have been synthesized and characterized by NMR and UV-vis spectroscopy as well as transmission electron microscopy (TEM). These NPs were irradiated in chloroform at different UV-wavelengths using either a nanosecond laser (266 and 355 nm, ca. 12 mJ/pulse, 10 ns pulse) or conventional lamps (300 nmλ400 nm and ca. 240 nmλ280 nm) and the new AuNPs were characterized by X-ray and UV-vis spectroscopy, as well as by TEM. Laser irradiation at 355 nm led to NP aggregation and precipitation,…

chemistry.chemical_classificationAnalytical chemistryNanoparticleSurfaces and InterfacesCondensed Matter PhysicsPhotochemistryPhthalimidechemistry.chemical_compoundchemistryTransition metalNanocrystalTransmission electron microscopyColloidal goldElectrochemistryBenzophenoneThiolGeneral Materials ScienceSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Pressure-Induced Polymerization of Polycyclic Arene-Perfluoroarene Cocrystals: Single Crystal X-ray Diffraction Studies, Reaction Kinetics, and Desig…

2020

Pressure-induced polymerization of aromatic compounds leads to novel materials containing sp3 carbon-bonded networks. The choice of the molecular species and the control of their arrangement in the crystal structures via intermolecular interactions, such as the arene–perfluoroarene interaction, can enable the design of target polymers. We have investigated the crystal structure compression and pressure-induced polymerization reaction kinetics of two polycyclic 1:1 arene–perfluoroarene cocrystals, naphthalene/octafluoronaphthalene (NOFN) and anthracene/octafluoronaphthalene (AOFN), up to 25 and 30 GPa, respectively, using single-crystal synchrotron X-ray diffraction, infrared spectroscopy, a…

chemistry.chemical_classificationAnthraceneStackingInfrared spectroscopyGeneral ChemistryPolymerCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographyColloid and Surface ChemistryPressure-induced polymerization; single-crystal synchrotron X-ray diffraction; high-pressure kinetic studychemistryPolymerizationX-ray crystallographySingle crystal
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Copolymers sensitive to temperature and pH in water and in water+oil mixtures: A DSC, ITC and volumetric study

2011

Block copolymer micelles are receiving an increasing interest because of the variety of structures and the possibilities to tune them by changing external and internal parameters achieving the desired properties for a specific purpose. We have investigated the acid/base behavior, self-assembling and solubilization ability towards polar oils of star-like copolymers named Tetronics. They are composed of branched four-arms each one consisting of two blocks made of EO and PO units linked to the diethylenediamine group, which confers pH response ability. The copolymers T1107 and T90R4 were studied with a sequential and reverse architecture. The thermodynamics of the acid/base equilibrium was stu…

chemistry.chemical_classificationAqueous solutionBase (chemistry)ChemistryCopolymers DSC ITC solubilizationMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface ChemistryDifferential scanning calorimetryMolar volumeChemical engineeringPulmonary surfactantCopolymerOrganic chemistryMacromoleculeJournal of Colloid and Interface Science
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Role of pH in the synthesis and growth of gold nanoparticles using L-asparagine: a combined experimental and simulation study

2020

Abstract The use of biomolecules as capping and reducing agents in the synthesis of metallic nanoparticles constitutes a promising framework to achieve desired functional properties with minimal toxicity. The system’s complexity and the large number of variables involved represent a challenge for theoretical and experimental investigations aiming at devising precise synthesis protocols. In this work, we use L-asparagine (Asn), an amino acid building block of large biomolecular systems, to synthesise gold nanoparticles (AuNPs) in aqueous solution at controlled pH. The use of Asn offers a primary system that allows us to understand the role of biomolecules in synthesising metallic nanoparticl…

chemistry.chemical_classificationAqueous solutionBiomoleculeMetal NanoparticlesWaterNanoparticle02 engineering and technologyHydrogen-Ion Concentration021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesMolecular dynamicsAdsorptionchemistryChemical engineeringColloidal gold0103 physical sciencesMonolayerMoleculeGeneral Materials ScienceGoldAsparagine010306 general physics0210 nano-technologyJournal of Physics: Condensed Matter
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Transfer of Some Alkyl Substituted Ferrocenes from Water to Cationic Surfactant Micelles Studied by Kinetic Method

1994

Abstract Binding of ferrocene and its 1,1′-dimethyl and n -butyl derivatives to dodecyl and tetradecyltrimethylammonium nitrate micellar aggregates has been studied at 20.0°C and ionic strength 0.02 tool dm -3 by examining the micellar retarding effects on the rates of iron(III) oxidation of these substrates. Solubilization of the ferrocenes in the cationic micellar phase increases as the substrate hydrophobic character increases and, to a lesser extent, as the surfactant hydrocarbon chain length becomes longer. The critical micelle concentrations of the surfactants used and the incremental free energy of transfer of methylene groups of both the substrate and the surfactant from the aqueous…

chemistry.chemical_classificationAqueous solutionChemistryInorganic chemistryCationic polymerizationMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantFerroceneIonic strengthMethyleneAlkylJournal of Colloid and Interface Science
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Enthalpies of Mixing of Some Primary Hydrogenated and Fluorinated Alcohols and Sodium Dodecanoate Aqueous Solutions

1993

Abstract The enthalpies of transfer from water to the surfactant solutions ΔH(W → W + S) of some hydrogenated and fiuorinated alkanols and of sodium dodecanoate NaL were determined. In the premicellar region the measurements were carried out as functions of both the additive and the surfactant concentrations in order to evaluate the interaction parameters between the additive and the surfactant molecules. It is shown that in this region, pair, triplet, and quadruplet interaction parameters between unlike solute molecules contribute to ΔH(W → W + S). Within the large uncertainty with which these parameters are determined because of the very narrow surfactant and alcohol concentration interva…

chemistry.chemical_classificationAqueous solutionDistribution constantEnthalpyConcentration effectSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsPropanolchemistry.chemical_compoundColloid and Surface ChemistrychemistryPulmonary surfactantPhysical chemistryOrganic chemistryAlkylHexanolJournal of Colloid and Interface Science
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Kinetic studies of the interaction between DNA and polycations based on polyasparthylhydrazide

2008

Abstract In the present paper, a systematic kinetic study on the interaction between interpolyelectrolytes such as positive-charged polymers and DNA was carried out. In particular, a qualitative–quantitative kinetic investigation on the interaction between copolymers of the α,β-poly(aspartylhydrazide) and DNA calf thymus filaments was performed. This study gives a new model starting from a well known “pseudo-phase model”, and permits to give a qualitative explanation about the trends of experimentally observed kinetic constants by varying the concentration of one of the two poly-electrolytes. Moreover, this study permits to verify the dependence of the binding constants KPAHy–CPTA and KDNA …

chemistry.chemical_classificationAqueous solutionKineticsCationic polymerizationThermodynamicsElectrolytePolymerKinetic energychemistry.chemical_compoundColloid and Surface ChemistrychemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoCopolymerOrganic chemistryDNA polycationsDNA
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Water-compatible molecularly imprinted polymers obtained via high-throughput synthesis and experimental design.

2003

A technique allowing high-throughput synthesis and evaluation of molecularly imprinted polymer sorbents at a reduced scale (mini-MIPs) was developed and used for the optimization of MIPs for use in pure aqueous environments. The technique incorporated a 4-port liquid-handling robot for the rapid dispensing of monomers, templates, solvents and initiator into the reaction vessels of a 96-well plate. A library of 80 polymers, each ca. 50 mg, could thus be prepared in 24 h. The MIP rebinding capacity and selectivity could be rapidly assessed in the batch mode by quantifying nonbound fractions in parallel using a UV monochromator plate reader. This allowed a complete evaluation of the binding ch…

chemistry.chemical_classificationAqueous solutionMolecularly imprinted polymerNanotechnologyGeneral ChemistryPolymerBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryTemplateMonomerMolecular recognitionchemistryChemical engineeringMolecular imprintingSelectivityJournal of the American Chemical Society
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Metachromatic behavior of methylorange in the presence of ionenes

1994

The addition of different ionenes, polycations with defined structure and charge distances, to methylorange1 in very dilute solutions of water resulted in an observable shift of the absorption maxima from 464 nm to shorter wavelengths. The extent of this so-called metachromasy effect was found to be dependent on the nature of the hydrophobic unit of the polymer backbone. The comparison of UV/VIS spectra's of these solutions with the absorption of a film of a model substance — a dication with methylorange as counteranion — lead to the conclusion that ionenes undergo an exchange of the counteranions when added to a dilute solution of methylorange. Precipitation is slowed down, but the absorpt…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsAbsorption spectroscopyConcentration effectPolymerPhotochemistryPolyelectrolyteIonDicationColloid and Surface ChemistrychemistryMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryAbsorption (chemistry)Colloid & Polymer Science
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A simple method to prepare solid nanoparticles of water-soluble salts using water-in-oil microemulsions

2000

A new and simple method to prepare solid nanoparticles of water-soluble salts using water-in-oil microemulsions is described. In particular, starting from water/sodium bis(2-ethylhexyl)sulfosuccinate/n-heptane microemulsions carrying inside the aqueous core of the reversed micelles some water-soluble salts [CaCl2, Na2HPO4, Cu(NO3)2], after evaporation of the volatile components (water and apolar organic solvent), the resulting inorganic salt/surfactant composites were found to be totally dispersible in pure n-heptane. The presence of nanoparticles in these resuspended composites was ascertained by transmission electron microscopy observation of samples obtained by gentle evaporation of the …

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsSodiumInorganic chemistryEvaporationchemistry.chemical_elementSalt (chemistry)NanoparticleMicelleColloid and Surface ChemistryPulmonary surfactantchemistryChemical engineeringMaterials ChemistryMicroemulsionPhysical and Theoretical ChemistryColloid & Polymer Science
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