Search results for "Propylene carbonate"

showing 10 items of 19 documents

Electrochemical reduction of graphene oxide films in aqueous and organic solutions

2013

Abstract Electrochemical reduction of graphene oxide (GO) films cast on tin oxide glass substrates were carried out in aqueous solutions and in propylene carbonate and acetonitrile. Cyclic voltammetric measurements indicate successful reduction of GO films. The reduction process begins in aqueous solutions at less negative potentials than in organic solutions. Additionally the pH value of the aqueous solutions influences the reduction potential. According to spectroscopic analysis the reduction process of the GO film can be controlled by the choice of reduction potential and electrolyte medium. The potential window in this work was made broader by increasing pH or by using organic electroly…

Aqueous solutionMaterials scienceGrapheneGeneral Chemical EngineeringInorganic chemistryOxideElectrolyteElectrochemistryTin oxidelaw.inventionchemistry.chemical_compoundchemistrylawPropylene carbonateElectrochemistryAcetonitrileta116Electrochimica Acta
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Efficient electroorganic synthesis of 2,3,6,7,10,11-hexahydroxytriphenylene derivatives

2012

2,3,6,7,10,11-Hexahydroxytriphenylene of good quality and purity can be obtained via anodic treatment of catechol ketals and subsequent acidic hydrolysis. The electrolysis is conducted in propylene carbonate circumventing toxic and expensive acetonitrile. The protocol is simple to perform and superior to other chemical or electrochemical methods. The key of the method is based on the low solubility of the anodically trimerized product. The shift of potentials is supported by cyclic voltammetry studies.

CatecholElectrolysishexahydroxytriphenyleneketalsOrganic Chemistrycatecholpropylene carbonateElectrochemistryFull Research Paperlaw.inventionlcsh:QD241-441Chemistrychemistry.chemical_compoundHydrolysischemistrylcsh:Organic chemistrylawPropylene carbonateOrganic chemistrylcsh:QCyclic voltammetrySolubilityelectrochemical oxidationAcetonitrilelcsh:ScienceBeilstein Journal of Organic Chemistry
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Asymmetric Hydrogenation of Nonfunctionalized Olefins in Propylene Carbonate—Kinetic or Thermodynamic Control?

2011

Iridium-catalyzed hydrogenations of nonfunctionalized olefins in propylene carbonate as the solvent allow efficient catalysis with much higher enantioselectivities in comparison with dichloromethane which is usually employed for these reactions. Experimental and computational studies of the hydrogenation of 1-methylene-1,2,3,4-tetrahydronaphthalene have been performed to understand the limitation for this reaction.

ChemistryGeneral Chemical EngineeringKineticsInorganic chemistryAsymmetric hydrogenationGeneral ChemistryKinetic energyIndustrial and Manufacturing EngineeringCatalysisSolventchemistry.chemical_compoundPropylene carbonateOrganic chemistryDichloromethaneIndustrial & Engineering Chemistry Research
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Predictability of drug encapsulation and release from propylene carbonate/PLGA microparticles.

2020

Abstract Key parameters for microparticle-based parenteral depot formulation development are entrapment efficiency and sustained drug release, which both depend on the intermolecular affinity of the components. Here, partial solubility parameters were evaluated as descriptors for 21 drug substances and 3 polymers in propylene carbonate (PC). Out of these 21 drug substances, eight BCS class II substances (celecoxib, clotrimazole, erythromycin, ibuprofen, indomethacin, itraconazole, lopinavir and ritonavir) were encapsulated using PLGA (Poly(DL-lactide-co-glycolide)) as polymer matrix and PC as a polar aprotic solvent in order to assign microparticle properties to potential affinity-related i…

Drug CompoundingPharmaceutical Science02 engineering and technology030226 pharmacology & pharmacy03 medical and health scienceschemistry.chemical_compoundPropane0302 clinical medicinePolylactic Acid-Polyglycolic Acid CopolymermedicineLactic AcidMicroparticleSolubilityParticle SizeChemistry021001 nanoscience & nanotechnologyIbuprofenMicrospheresSolventHildebrand solubility parameterPLGAChemical engineeringPharmaceutical PreparationsSolubilityPropylene carbonate0210 nano-technologyGlass transitionPolyglycolic Acidmedicine.drugInternational journal of pharmaceutics
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Microparticle preparation by a propylene carbonate emulsification-extraction method

2018

Abstract The use of various harmful organic solvents for microparticle formulations is still widespread. Here, an alternative low toxicity solvent (propylene carbonate; PC) is proposed for the preparation of poly(lactic-co-glycolic-acid) (PLGA) microparticles. Based on the classical emulsification-solvent extraction methodology, the use of PC offers the unique advantage of an additional solvent extraction step using hydrolytic solvent cleavage during microparticle preparation. Spherical, rough-surfaced microparticles were obtained with a volume median diameter range from 20 to 60 µm. The residual PC content has been identified to be the major factor for the solidification hindrance, leading…

Drug CompoundingPolysorbatesPharmaceutical Science02 engineering and technology010402 general chemistry01 natural sciencesPropanechemistry.chemical_compoundHydrolysisPolylactic Acid-Polyglycolic Acid CopolymerLactic AcidMicroparticleLow toxicityExtraction (chemistry)021001 nanoscience & nanotechnology0104 chemical sciencesSolventPLGAchemistryChemical engineeringPropylene carbonateSolventsEmulsionsExtraction methods0210 nano-technologyPolyglycolic AcidInternational Journal of Pharmaceutics
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Slow and fast methyl group rotations in fragile glass-formers studied by NMR

2000

Abstract The spin-lattice relaxation times of the selectively ring deuterated, fragile glass-formers propylene carbonate and toluene were compared with those measured for species which were specifically labeled at the methyl groups. It was found that the dynamics of the CD 3 group is strongly decoupled from that associated with the primary response of toluene, while for propylene carbonate the degree of decoupling is relatively weak. The experimental results could be described successfully using a model which takes into account the ring dynamics as well as those of the methyl group.

Inorganic chemistryRelaxation (NMR)Primary responseGeneral Physics and AstronomyRing (chemistry)Toluene530Condensed Matter::Disordered Systems and Neural NetworksCondensed Matter::Soft Condensed MatterCrystallographychemistry.chemical_compoundchemistryDeuteriumGroup (periodic table)Propylene carbonatePhysical and Theoretical ChemistryPhysics::Chemical PhysicsMethyl group
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Pegylated nanoparticles based on a polyaspartamide. Preparation, physico-chemical characterization and intracellular uptake

2006

Nanoparticles with different surface PEGylation degree were prepared by using as starting material alpha,beta-poly(N-2-hydroxyethyl)-d,l-aspartamide (PHEA). PHEA was functionalized with a PEG amino-derivative for obtaining PHEA-PEG(2000) copolymer. Both PHEA and PHEA-PEG(2000) were derivatized with methacrylic anhydride (MA) for obtaining poly(hydroxyethylaspartamide methacrylated) (PHM) and poly(hydroxyethylaspartamide methacrylated)-PEGylated (PHM-PEG(2000)), respectively. Nanoparticles were obtained by UV irradiation of an inverse microemulsion, using as internal phase an aqueous solution of PHM alone or of the PHM/PHM-PEG(2000) mixture at different weight ratio and as external phase a m…

Magnetic Resonance SpectroscopyPolymers and PlasticsUltraviolet RaysNanoparticleMethacrylic anhydrideBioengineeringPolyethylene GlycolsBiomaterialschemistry.chemical_compoundMicroscopy Electron TransmissionPEG ratioPolymer chemistrySpectroscopy Fourier Transform InfraredMaterials ChemistryZeta potentialHumansMicroemulsionParticle SizeNanoparticlesalphabeta-poly(N-2-hydroxyethyl)-dl-aspartamide (PHEA)methacrylic anhydride.Aqueous solutionchemistryPropylene carbonatePEGylationMethacrylatesNanoparticlesK562 CellsPeptidesNuclear chemistry
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Ionic conduction through single-pore and multipore polymer membranes in aprotic organic electrolytes

2021

Abstract We experimentally characterize the ionic conduction of single and multipore nanoporous membranes in aprotic organic electrolytes. To this end, soft-etched (SE) membranes with pore diameters in the nanometer range and track-etched (TE) membranes with pore diameters in the tens of nanometers range are investigated. In aqueous conditions, the membrane ionic conduction rates follow the same trend of the bulk solution conductivities. However, the ionic transport through the narrow SE-nanopores dramatically decreases in aprotic electrolytes due to the formation of solvated metal cations and their adsorption on the pore surface. The current-voltage recordings of single conical nanopores i…

Materials scienceAqueous solutionSynthetic membraneIonic bondingFiltration and Separation02 engineering and technologyElectrolyte010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundMembranechemistryChemical engineeringPropylene carbonateIonic conductivityGeneral Materials SciencePhysical and Theoretical Chemistry0210 nano-technologyAcetonitrileJournal of Membrane Science
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Process parameters of microsphere preparation based on propylene carbonate emulsion-precursors.

2020

This study aimed for a detailed understanding of the impact of different process parameters involved during celecoxib-loaded microsphere preparation based on propylene carbonate emulsion-precursors.Microspheres were prepared by a modified emulsification-solvent extraction method. Performed investigations included polymer solubility and viscosity, microsphere size, morphology and stability, propylene carbonate content as well as celecoxib solid state, content and release.Rough-walled round microspheres with sizes between 21 µm and 122 µm and an internal sponge-like structure filled with residual propylene carbonate (content between 1.9 ± 0.1% and 6.7 ± 0.5% w/w) were obtained. Encapsulation …

Materials sciencePolymersSurface PropertiesChemistry PharmaceuticalDrug CompoundingPharmaceutical ScienceBioengineering02 engineering and technologyPolypropylenes030226 pharmacology & pharmacyMicrosphere03 medical and health scienceschemistry.chemical_compound0302 clinical medicineColloid and Surface ChemistryLactic AcidPhysical and Theoretical ChemistryParticle SizeDrug CarriersCalorimetry Differential ScanningViscosityOrganic Chemistry021001 nanoscience & nanotechnologyMicrospheresPLGADrug LiberationchemistryChemical engineeringSolubilityCelecoxibScientific methodPropylene carbonateEmulsionMicroscopy Electron ScanningSolventsEmulsions0210 nano-technologyPolyglycolic AcidJournal of microencapsulation
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Nonresonant Spectral Hole Burning in the Slow Dielectric Response of Supercooled Liquids

1996

Large-amplitude, low-frequency electric fields can be used to burn spectral holes in the dielectric response of supercooled propylene carbonate and glycerol. This ability to selectively modify the dielectric response establishes that the non-Debye behavior results from a distribution of relaxation times. Refilling of the spectral hole was consistent with a single recovery time that coincided with the peak in the distribution. Moreover, refilling occurred without significant broadening, which indicates negligible direct exchange between the degrees of freedom that responded to the field. Nonresonant spectral hole burning facilitates direct investigation of the intrinsic response of systems t…

PermittivityMultidisciplinaryField (physics)Oscillationbusiness.industryRelaxation (NMR)Molecular physicschemistry.chemical_compoundOpticschemistryElectric fieldPropylene carbonateSpectral hole burningDielectric lossbusinessScience
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