Search results for "Vapo"

showing 10 items of 1217 documents

Plasmonic optical sensors printed from Ag–PVA nanoinks

2014

In this paper we report on the use of a nanocomposite based on silver nanoparticles embedded in PVA as a plasmonic optical sensor to detect and quantify trace amounts of amines in gas and water, respectively. The transduction mechanism of the sensor is based on the changes of the LSPR band of Ag NPs when analyte molecules are chemisorbed on their surface. The Ag–PVA sensors are fabricated by means of a high-precision microplotter, a direct-write technology developed for printing materials from solution. The nanoink is formulated with a metal precursor (AgNO3) and a polymer (PVA) using an adequate mixture of solvents to meet the rheological requirements for the fluid dispensing process. The …

chemistry.chemical_classificationDetection limitNanocompositeMaterials scienceActive packagingNanotechnologyEthylenediamineGeneral ChemistryPolymermedicine.diseaseSilver nanoparticlechemistry.chemical_compoundchemistryMaterials ChemistrymedicinePlasmonVapoursJ. Mater. Chem. C
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Biofiltration of ethylbenzene vapours: influence of the packing material.

2006

In order to investigate suitable packing materials, a soil amendment composed of granular high mineralized peat (35% organic content) locally available has been evaluated as carrier material for biofiltration of volatile organic compounds in air by comparison with a fibrous peat (95% organic content). Both supports were tested to eliminate ethylbenzene from air streams in laboratory-scale reactors inoculated with a two-month conditioned culture. In pseudo-steady state operation, experiments at various ethylbenzene inlet loads (ILs) were carried out. Maximum elimination capacity of about 120 g m(-3) h(-1) for an IL of 135 g m(-3) h(-1) was obtained for the fibrous peat. The soil amendment re…

chemistry.chemical_classificationEnvironmental EngineeringPeatSoil testRenewable Energy Sustainability and the EnvironmentChemistryEnvironmental engineeringAmendmentBioengineeringGeneral MedicineBiodegradationModels Theoreticalmedicine.diseasePulp and paper industryEthylbenzenechemistry.chemical_compoundSoilSpainBiofiltermedicineBenzene DerivativesVolatile organic compoundWaste Management and DisposalVapoursFiltrationBioresource technology
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Die bestimmung der molekulargewichtsverteilung von nichtkristallisierenden polymeren mit dem elektronenmikroskop, 7. Präparation durch verdampfung de…

1977

A preparation method is described by means of which it is possible to transfer individual molecules of a high molecular weight polymer on a support, in order to determine their mass and therefrom their molecular weight distribution, using our previously published electron microscopic method. The advantages of the new procedure as compared to the previously described freeze-drying are 1 that the range of solvents, which can be used is much larger, and 2 that the preparation is performed by evaporation from a dilute solution, which means that the molecules are distributed statistically on the support. The risk of formation of associates is avoided by keeping the polymer concentration correspo…

chemistry.chemical_classificationEvaporationPolymerPreparation methodchemistry.chemical_compoundchemistryNatural rubbervisual_artPolymer chemistryvisual_art.visual_art_mediumMoleculeMolar mass distributionMethyl methacrylateElectron microscopicDie Makromolekulare Chemie
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Saturated vapour pressure of aroma compounds at various temperatures

2004

Abstract The aim of this study was to determine experimentally the vapour pressures of aroma compounds at various temperatures, especially at negative ones. The aroma compounds were: acetone, 2-butanone, 2-hexanone, 2-octanone, ethyl acetate, ethyl butanoate, ethyl hexanoate, n-hexanal, n-hexanol and γ-hexalactone. The technique used was a static device where vapour pressure was measured at equilibrium. The temperatures of analysis varied from −40 to 25 °C. Volatility of a pure compound depends on characteristics such as length of the aliphatic chain, the functional group and temperature. Among an homologous series, volatility increases when the aliphatic chain decreases and when temperatur…

chemistry.chemical_classificationKetonebiologyVapor pressureInorganic chemistryEthyl acetateEthyl hexanoateGeneral Medicinebiology.organism_classificationAnalytical Chemistrychemistry.chemical_compoundHomologous serieschemistryAcetoneOrganic chemistryVolatility (chemistry)AromaFood ScienceFood Chemistry
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Perovskite solar cells prepared by flash evaporation

2015

A simple vacuum deposition method for the preparation of high quality hybrid organic-inorganic methylammonium lead iodide perovskite thin films is reported. When sandwiched in between organic charge transporting layers, such films lead to solar cells with a power conversion efficiency of 12.2%.

chemistry.chemical_classificationMaterials scienceF100IodideInorganic chemistryEnergy conversion efficiencyF200Metals and AlloysFlash evaporationGeneral ChemistryHybrid solar cellCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryChemical engineeringVacuum depositionMaterials ChemistryCeramics and CompositesThin filmPerovskite (structure)Chemical Communications
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Isobornyl Methacrylate as a Reactive Solvent of Polyethylene

2004

Solutions containing 15 wt, -% of a low-molar-mass polyethylene (PE) in isobornyl methacrylate (IBoMA), containing 0, 5 or 10 wt.-% of 1,4 butanediol dimethacrylate (BDDMA) as crosslinker, were polymerized using either benzoyl peroxide (BPO), at 80°C, or dicumyl peroxide (DCPO), with a thermal cycle attaining 150°C, as initiators. Phase separation of an amorphous PE-rich phase took place when carrying out the reaction at temperatures higher than the PE melting temperature. Partial crystallization of PE was observed when cooling to room temperature. Depending on the initial amount of BDDMA, the fraction of PE that was phase separated varied between 57 and 66% of the initial amount, with crys…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsVapor pressureGeneral Chemical EngineeringOrganic ChemistryBenzoyl peroxidePolymerPolyethylenelaw.inventionSolventchemistry.chemical_compoundChemical engineeringchemistryPolymerizationlawPolymer chemistryMaterials ChemistrymedicineCrystallizationGlass transitionmedicine.drugMacromolecular Materials and Engineering
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Sorption of n-hexane in amorphous polystyrene

2014

Sorption properties of pure n-hexane vapor in amorphous polystyrene (PS) were studied at 298 K by thermogravimetry under controlled vapor pressure. Two sorption-desorption cycles were performed by varying the relative pressure between 0 and 0.91. Mixing of PS with n-hexane resulted in a strong plasticization, which was evidenced by quite significant depression in the glass transition temperature of the polymer as shown by differential scanning calorimetry. Maximum quantity of n-hexane sorbed in the PS at 298 K and at a pressure close to saturation was about 12.4 wt %. The thermogravimetry yielded an isotherm with a strong hysteresis loop, explanation of which was hypothesized with the help …

chemistry.chemical_classificationMaterials sciencePolymers and Plastics[ SDV ] Life Sciences [q-bio]Vapor pressureamorphous[SDV]Life Sciences [q-bio]Analytical chemistrySorptionPolymerCondensed Matter PhysicsAmorphous solidThermogravimetrychemistry.chemical_compoundswellingDifferential scanning calorimetryGlassy PolystyrenechemistryPolymer chemistryMaterials Chemistrysorption hysteresisPolystyrenestructurePhysical and Theoretical ChemistryGlass transition
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Formation of micro- and nano-spheric particles (filter dust) during the preparation of cellulose acetate membranes

2003

Abstract Membranes were prepared from six samples of cellulose acetate (CA) differing in their average molecular weight (75–260 kg/mole) and molecular weight distribution using methyl acetate as solvent and 2-propanole as precipitant. The routes through the phase diagram and the evaporation times were varied in these experiments. Electron microscopy demonstrates that the amount of filter dust (CA particles deposited on the membrane surface) decreases as the fraction of low molecular weight material in the starting polymer becomes less. For low average molar mass of CA and moderate polymer concentrations in the casting solution the dust consists of individual spheres of relatively uniform si…

chemistry.chemical_classificationMolar massMaterials scienceMethyl acetateEvaporationFiltration and SeparationPolymerBiochemistryCastingCellulose acetatechemistry.chemical_compoundMembranechemistryChemical engineeringPolymer chemistryMolar mass distributionGeneral Materials SciencePhysical and Theoretical ChemistryJournal of Membrane Science
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Removal of TEX vapours from air in a peat biofilter: influence of inlet concentration and inlet load

2006

This paper presents the results of the study of the removal of toluene, ethylbenzene, and o-xylene (TEX) by biofiltration using a commercial peat as filter-bed material. Runs with a single organic compound in air, and with the mixture of TEX in air, were carried out for at least 55 days in laboratory-scale reactors inoculated with a conditioned culture. The influence of organic compound inlet load and of gas flow rate on the biofilter's performance was studied, including relatively high values of pollutant inlet concentration (up to 4.3 gC m−3 for ethylbenzene, 3.2 gC m−3 for toluene, and 2.7 gC m−3 for o-xylene). Results obtained show maximum elimination capacities of 65 gC m−3 h−1 for o-x…

chemistry.chemical_classificationPollutantRenewable Energy Sustainability and the EnvironmentGeneral Chemical EngineeringOrganic Chemistrymedicine.diseasePollutionOrganic compoundTolueneEthylbenzeneVolumetric flow rateInorganic Chemistrychemistry.chemical_compoundFuel TechnologychemistryEnvironmental chemistryBiofiltermedicineVolatile organic compoundWaste Management and DisposalVapoursBiotechnologyJournal of Chemical Technology & Biotechnology
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Branched Versus Linear Polyisoprene: Flory-Huggins Interaction Parameters for their Solutions in Cyclohexane

2009

Flory-Huggins interaction parameters were determined as a function of composition for solutions of linear and of branched polyisoprene in cyclohexane (CH) at 25, 45, and 65 °C by means of vapor pressure measurements (moderate to concentrated solutions) and by vapor pressure osmometry (dilute solutions). The results demonstrate that CH is a considerably worse solvent for branched polyisoprene than for the linear analog at all temperatures and at all compositions. This observation corroborates the expectation based on a recent phenomenological approach, which accounts explicitly for the incapability of the segments of an individual polymer molecule to spread out over the entire volume of the …

chemistry.chemical_classificationPolymers and PlasticsCyclohexaneVapor pressureVapor pressure osmometryOrganic ChemistryConcentration effectPolymerFlory–Huggins solution theoryCondensed Matter Physicschemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryMoleculeBinary systemPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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