Search results for "fluid"

showing 10 items of 5513 documents

Supercritical Assisted Atomization: Polyvinylpyrrolidone as Carrier for Drugs with Poor Solubility in Water

2013

Supercritical assisted atomization (SAA) is an efficient technique to produce microparticles and composite microspheres formed by polymers and pharmaceutical compounds. In this work polyvinylpyrrolidone (PVP) was proposed as carrier for pharmaceutical compounds that show a poor solubility in water medium. Indeed, this polymer is hydrosoluble and can be generally used to enhance the dissolution rate of hydrophobic compounds when finely dispersed in it. However, it is difficult to obtain coprecipitates with a uniform dispersion of the active molecule using other micronization techniques. The experiments were performed using ethanol as solvent; SAA plant was operated at 40°C and 76 bar in the …

chemistry.chemical_classificationChromatographyArticle SubjectPolyvinylpyrrolidoneSettore ING-IND/25 - Impianti ChimiciGeneral ChemistryPolymerSupercritical fluidlcsh:ChemistrySolventSupercritical fluids atomization drug particleslcsh:QD1-999chemistryChemical engineeringmedicineSolubilityMicronizationDispersion (chemistry)Dissolutionmedicine.drug
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Selective protein removal and desalting using microchip CE.

2006

Abstract This paper describes the on-line sample pretreatment and analysis of proteins and peptides with a poly(methylmethacrylate) (PMMA) microfluidic device (IonChip™). This chip consists of two hyphenated electrophoresis channels with integrated conductivity detectors. The first channel can be used for sample preconcentration and sample clean-up, while in the second channel the selected compounds are separated. Isotachophoresis (ITP) combined with zone electrophoresis (CZE) was used to preconcentrate a myoglobin sample by a factor of about 65 before injection into the second dimension and to desalt a mixture of six proteins with 100 mM NaCl. However, ITP–CZE could not be used for the rem…

chemistry.chemical_classificationChromatographyChemistryClinical BiochemistryMicrofluidicsAnalytical chemistryA proteinProteinsPeptideCell BiologyGeneral MedicineBiochemistrySample (graphics)Online SystemsAnalytical ChemistryElectrophoresis Microchipchemistry.chemical_compoundElectrophoresisMyoglobinAnimalsHumansIsotachophoresisJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Application of molecularly imprinted polymers in supercritical fluid chromatography

2000

Molecularly imprinted polymers (MIPs), for the templates free base racemic propranolol and the L-enantiomer of phenylalanine anilide (L-PA), were investigated as stationary phases in supercritical fluid chromatography (SFC). Large retention differences were observed on the propranolol MIP for both the template molecule and the structural analogue metoprolol compared to that observed on the corresponding blank polymer. Mobile phase composition and solute concentration were found to affect this retention behaviour. The phenylalanine anilide MIP (L-PA MIP) was found to be enantioselective in SFC with stronger retention observed for the template enantiomer. Throughout the study, characteristic …

chemistry.chemical_classificationChromatographyChromatographyPolymersOrganic ChemistryMolecularly imprinted polymerFree baseGeneral MedicinePolymerPropranololBiochemistryHigh-performance liquid chromatographySupercritical fluidAnalytical ChemistrychemistrySupercritical fluid chromatographyEnantiomerMolecular imprintingChromatography High Pressure LiquidJournal of Chromatography A
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Phase behavior of the system hyperbranched polyglycerol+methanol+carbon dioxide

2010

Abstract Phase equilibrium data have been measured for the ternary system hyperbranched polyglycerol + methanol + carbon dioxide at temperatures of 313–450 K and pressures up to 13.5 MPa. Phase changes were determined according to a synthetic method using the Cailletet setup. At elevated temperatures the system shows a liquid–liquid–vapor region with lower solution temperatures. Besides the vapor–liquid and liquid–liquid equilibria, the vapor–liquid to vapor–liquid–liquid and vapor–liquid–liquid to liquid–liquid phase boundaries are reported at different polymer molar masses and can serve as test sets for thermodynamic models. A distinct influence of the polymer molar mass on the vapor–liqu…

chemistry.chemical_classificationCloud pointEquation of stateTernary numeral systemMolar massGeneral Chemical EngineeringGeneral Physics and AstronomyThermodynamicsPolymerBranching (polymer chemistry)Physics::Fluid DynamicsCondensed Matter::Soft Condensed MatterchemistryOrganic chemistryBubble pointPhysical and Theoretical ChemistryPhase diagramFluid Phase Equilibria
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Lattice fluid model generalized for specific interactions: An application to ternary polymer solutions

2011

Abstract The phase diagram of the Poly- l -Lactic-Acid (PLLA), dioxane and water system was derived by using the lattice fluid model generalized for specific interactions. A qualitative analysis of Hansen solubility parameters together with empirical observations were adopted to reduce the number of adjustable parameters. The as-selected model parameters were derived by fitting a set of cloud point curves; consequently, the complete phase diagram of the system was computed. The use of specific interactions between species gave out a quantitative agreement with a set of experimental data, whereas changing the polymer polydispersity the agreement is only qualitative. In principle, the present…

chemistry.chemical_classificationCloud pointGeneral Chemical EngineeringLiquid–liquid equilibriaDispersityPhase separationGeneral Physics and AstronomyThermodynamicsExperimental dataPolymerPolymer solutionSet (abstract data type)Lattice fluid modelHildebrand solubility parameterchemistryPhysical and Theoretical ChemistryTernary operationPhase diagramFluid Phase Equilibria
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Contour-Variable Model of Constitutive Equations for Polymer Melts

2009

Based on a modified expression of the rate of the convective constraint release, we present a new contour-variable model of constitutive equations in which the non-uniform segmental stretch and the non-Gaussian chain statistical treatment of the single chain are considered to describe the polymer chain dynamics and the rheological behavior of an entangled system composed of linear polymer chains. The constitutive equations are solved numerically in the cases of steady shear and transient start-up of steady shear. The results indicate that the orientation and stretch, as well as the tube survival probability, have strong dependence on the chain contour variable, especially in the high-shear-…

chemistry.chemical_classificationConvectionMaterials sciencePolymers and PlasticsOrganic ChemistryDynamics (mechanics)Constitutive equationFluid Dynamics (physics.flu-dyn)FOS: Physical sciencesPolymerMechanicsPhysics - Fluid DynamicsConstraint (information theory)Condensed Matter::Soft Condensed MatterRheologyChain (algebraic topology)chemistryMaterials ChemistryVariable (mathematics)
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Influence of the process variables on the product distribution and catalyst decay during cracking of paraffins

1986

Abstract The influence of the partial pressure of the hydrocarbon, reaction temperature, time on stream and the presence of olefins on the product distribution and the kinetics and decay during the cracking of n-heptane on an REHY zeolite were studied. It was found that the isomerization to cracking ratio depends on the hydrocarbon partial pressure. The active sites for cracking and isomerization are not the same and those for cracking decay faster, the selectivity changing with the degree of decay of the zeolite. The protolytic to β-cracking ratio, and therefore the paraffin to olefin ratio, are a function of the partial pressure of n-heptane. Both reactants and products have a marked infl…

chemistry.chemical_classificationCrackingHydrocarbonChemical engineeringchemistryGeneral EngineeringPartial pressurePhotochemistryZeoliteFluid catalytic crackingIsomerizationProduct distributionCatalysisApplied Catalysis
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Modelling small angle neutron scattering data from polymers in supercritical fluids

2000

In this paper we report a SANS investigation of micelle formation by fluorocarbon-hydrocarbon block copolymers in supercritical CO2(scCO2) at 313K. A sharp unimer-micelle transition is obtained due to the tuning of the solvating ability of scCO2 by profiling pressure. At high pressure the copolymer is in a monomeric state with a random coil structure. By lowering the pressure aggregates are formed with the hydrocarbon segments forming the core and the fluorocarbon segments forming the corona of spherical aggregates. This aggregate-unimer transition is driven by the gradual penetration of CO2 molecules toward the core of the aggregate and is critically related to the density of the solvent, …

chemistry.chemical_classificationCrystallographyMaterials sciencechemistryChemical physicsCopolymerSolvationPolymerFluorocarbonSmall-angle neutron scatteringMicelleSupercritical fluidRandom coilAIP Conference Proceedings
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Model Eye Incorporating a Manually Tunable Polymer Lens and Microfluidics Chamber for Simulation of Vitreous Floaters

2016

a model eye incorporating a manually tunable lens and microfluidics chamber for simulation of vitreous floaters has been described. Aberrations correspond to average values in population and diffraction effects could be observed.

chemistry.chemical_classificationDiffractioneducation.field_of_studyMaterials sciencegenetic structuresbusiness.industryMicrofluidicsPopulationAqueous humorPolymereye diseasesPtychographyVitreous Floater030218 nuclear medicine & medical imaginglaw.inventionLens (optics)03 medical and health sciences0302 clinical medicineOpticschemistrylaw030221 ophthalmology & optometrysense organsbusinesseducationImaging and Applied Optics 2016
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Hydrothermal liquefaction of waste biomass in stirred reactors: One step forward to the integral valorization of municipal sludge

2020

Abstract Hydrothermal liquefaction (HTL) of municipal sludge (MS) was performed at 350 °C for 30 min (subcritical water) and at 400 °C for 0 min (supercritical water) at fixed kinetic severity (LogR0 = 8.9) in static and stirred batch reactors to study the effect of the flow regime on the energy recovery (ER) of the process and on the quality of the products. With adopted experimental procedures it was possible to reduce to less than 10% the yield of lost organic compounds, termed volatiles (VT), and to collect and quantify a liquid hydrocarbon fraction (HC) separated from the biocrude (BC). The highest value of the HC yield, 25% w/w, was obtained in supercritical conditions. The C content …

chemistry.chemical_classificationEnergy recovery020209 energyMechanical EngineeringBiomassFraction (chemistry)02 engineering and technologyBuilding and ConstructionPulp and paper industryPollutionIndustrial and Manufacturing EngineeringSupercritical fluidHydrothermal liquefactionGeneral EnergyHydrocarbon020401 chemical engineeringchemistryBiofuelYield (chemistry)0202 electrical engineering electronic engineering information engineering0204 chemical engineeringElectrical and Electronic EngineeringBiofuelEnergy recovery Energy storage Hydrothermal liquefaction Municipal sludge Waste biomassCivil and Structural Engineering
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