Search results for "PLASTICS"

showing 10 items of 2724 documents

Polysaccharide nanocrystals as fillers for PLA based nanocomposites

2016

The development of green nanocomposites based on biopolymers and bio-based nanofillers has attracted over the recent years the attention of academic and industrial research. Indeed, these nanocomposites could replace some oil-derived polymers and thus helping to overcome environmental problems. In this regard, PLA as matrix and polysaccharide nanocrystals as fillers are the most promising components to obtain high-performance green bio-nanocomposites suitable for different applications, particularly for packaging and biomedical applications. Indeed, at present, due to its processability, mechanical and biological properties, as well as its commercial availability, poly(lactic acid) (PLA) po…

Cellulose nanocrystals (CNCs)Materials sciencePolymers and PlasticsStarchNanotechnologyChitin nanocrystals (ChNCs)02 engineering and technology010402 general chemistryPolysaccharide01 natural sciencesPoly(lactic acid) (PLA)chemistry.chemical_compoundChitinCellulosePolysaccharide nanocrystalchemistry.chemical_classificationNanocompositeNanocompositePolymerBiodegradation021001 nanoscience & nanotechnologyStarch nanocrystals (SNCs)0104 chemical sciencesSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNanocrystalchemistry0210 nano-technology
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Dynamic Self-Consistent Field Approach for Studying Kinetic Processes in Multiblock Copolymer Melts

2020

The self-consistent field theory is a popular and highly successful theoretical framework for studying equilibrium (co)polymer systems at the mesoscopic level. Dynamic density functionals allow one to use this framework for studying dynamical processes in the diffusive, non-inertial regime. The central quantity in these approaches is the mobility function, which describes the effect of chain connectivity on the nonlocal response of monomers to thermodynamic driving fields. In a recent study [Mantha et al, Macromolecules 53, 3409 (2020)], we have developed a method to systematically construct mobility functions from reference fine-grained simulations. Here we focus on melts of linear chains …

Chemical Physics (physics.chem-ph)Physicsordering kineticsMesoscopic physicsPolymers and PlasticsField (physics)Thermodynamic equilibriumDynamic structure factorFOS: Physical sciencesNon-equilibrium thermodynamicsContext (language use)General ChemistryCondensed Matter - Soft Condensed MatterDynamic densityArticlelcsh:QD241-441lcsh:Organic chemistrydynamic density functional theoryPhysics - Chemical Physicstwo-length scale copolymerssingle chain structure factorSoft Condensed Matter (cond-mat.soft)Density functional theoryStatistical physicsmultiblock copolymersPolymers
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New Lignocellulosic Aristida adscensionis Fibers as Novel Reinforcement for Composite Materials: Extraction, Characterization and Weibull Distributio…

2019

In this research, the Aristida adscensionis fibers (AAFs) were taken out from the plants and its fundamental properties anlayzed for the first time. The AAFs were characterized and compared with other natural fibers by the use of physico-chemical analysis and various characterization techniques such as FT-IR, XRD, NMR, TGA, SEM and AFM. Chemical analysis showed that A. adscensionis fibers have a high cellulose content of 70.78% whereas the contents of lignin and wax are equal to 8.91% and 2.26%, respectively. The FT-IR, XRD and NMR analysis confirmed that AAFs are rich in cellulose content with CI and CS equal to 58.9% and 11.5 nm, respectively. Pycnometer analysis allowed to estimate a den…

Chemical analysiEnvironmental EngineeringMaterials sciencePolymers and PlasticsCharacterizationAristida adscensionisExtraction02 engineering and technologySingle fiber tensile testchemistry.chemical_compound020401 chemical engineeringUltimate tensile strengthMaterials ChemistryLigninFiber0204 chemical engineeringCelluloseComposite materialWeibull distributionWaxbiologyExtraction (chemistry)021001 nanoscience & nanotechnologybiology.organism_classificationSettore ING-IND/22 - Scienza E Tecnologia Dei Materialichemistryvisual_artvisual_art.visual_art_mediumPhysical analysi0210 nano-technologyAristida adscensionis fiber
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Direct identification of 103–107Mo by a rapid chemical separation procedure

1977

Abstract The nuclides 103–107Mo have been identified by means of γ-ray spectroscopy after the separation of molybdenum from fission products of 235U and 239Pu by a rapid chemical procedure. Half-lives of 67.5 ± 1.5 s for 103Mo, 59.4 ± 0.8 s for 104Mo, 36.7 ± 1.0 s for 105Mo, 8.4 ± 0.5 s for 106Mo and 3.5 ± 0.5 s for 107Mo have been determined and the main γ-lines were assigned to the decay of these isotopes. Some evidence for 108Mo with a half-life ≤2 s has also been obtained.

Chemical procedureChemical separationFission productsPolymers and PlasticsIsotopeChemistryMolybdenumMaterials ChemistryAnalytical chemistrychemistry.chemical_elementNuclideSpectroscopyJournal of Inorganic and Nuclear Chemistry
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Pullulan and dextran: uncommon composition dependent Flory-Huggins interaction parameters of their aqueous solutions.

2008

Vapor pressure measurements were performed for aqueous solutions of pullulan ( M w 280 kg/mol) and dextran ( M w 60 and 2100 kg/mol, respectively) at 25, 37.5, and 50 degrees C. The Flory-Huggins interaction parameters obtained from these measurements, plus information on dilute solutions taken from the literature, show that water is a better solvent for pullulan than for dextran. Furthermore, they evince uncommon composition dependencies, including the concurrent appearance of two extrema, a minimum at moderate polymer concentration and a maximum at high polymer concentration. To model these findings, a previously established approach, subdividing the mixing process into two clearly separa…

Chromatography GasPolymers and PlasticsVapor pressureThermodynamicsBioengineeringFlory–Huggins solution theoryBiomaterialschemistry.chemical_compoundMaterials ChemistryPressureSolubilityGlucanschemistry.chemical_classificationAqueous solutionChromatographyWaterPullulanDextransPolymerSolventMolecular WeightDextranchemistryModels ChemicalSolventsThermodynamicsBiomacromolecules
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Interaction of polyelectrolytes with oppositely charged micelles studied by fluorescence and liquid chromatography

2005

It is studied by spectrofluorimetry the association of ionized cationic micelles (cetyltrimethylammonium bromide, CTAB) with oppositely charged polyelectrolyte [sodium poly(styrenesulfonate), PSSNa]. CTAB provokes a change in the fluorescence intensity emitted by PSSNa. The investigated surfactants form micelle-like aggregates before critical micellar concentration (CMC). Two approaches (binding and partition equilibrium) are used to obtain the association constant, KA, number of CTAB molecules in a binding site, N, and apparent partition coefficient, Γ. Analysis of the parameters as a function of polymer concentration and ionic strength μ is performed. The effect of μ shows an enhancement …

ChromatographyAqueous solutionPolymers and PlasticsChemistryOrganic ChemistryGeneral Physics and AstronomyMicellePolyelectrolytePartition coefficientchemistry.chemical_compoundBromideIonic strengthPartition equilibriumCritical micelle concentrationMaterials ChemistryEuropean Polymer Journal
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New insights on the thermal analysis of low moisture composite foods.

2014

Abstract Low moisture baked products were investigated with a view to characterising the effect of both formulation and humidity on their physical stability. At the end of the baking process, the samples were in the amorphous state as a result of starch gelatinization and sugar melting. Their thermal properties were analyzed with differential scanning calorimetry and their glass transitions were studied. The DSC thermograms were thoroughly studied through a Gaussian deconvolution of the first derivative of their heat flow. This approach evidenced a multiple phase behavior with different glass transitions in composite systems. They were associated with either a polymer-rich phase and/or a pl…

ChromatographyMaterials sciencePolymers and PlasticsMoistureCalorimetry Differential ScanningOrganic ChemistryComposite numberFlourCarbohydratesTemperatureHumidityAmorphous solidStarch gelatinizationDifferential scanning calorimetryChemical engineeringPhase (matter)Materials ChemistryThermal analysisGlass transitionFood AnalysisCarbohydrate polymers
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MALDI-TOF characterization of macromonomers

1996

Methacryloyl endfunctionalized oligostyrene macromonomers were characterized by matrix assisted laser desorption ionization/time of flight (MALDI-TOF) spectroscopy and by isocratic and gradient high performance liquid chromatography (HPLC). The molar mass distribution derived by the different techniques coincide for the investigated oligomers. Mixing experiments revealed that the MALDI-TOF peak areas do not necessarily represent the mixing ratio of the components. Combination of gradient HPLC and MALDI-TOF has resolved the chemical composition of the coupling products formed by reaction of the living anion with oxygen.

ChromatographyPolymers and PlasticsChemistryOrganic ChemistryMatrix isolationAnalytical chemistryMass spectrometryMacromonomerHigh-performance liquid chromatographyTime of flightMatrix-assisted laser desorption/ionizationMaterials ChemistryMolar mass distributionSpectroscopyMacromolecular Rapid Communications
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Liquid/Gas and Liquid/Liquid Phase Behavior of n-Butane/1,4-Polybutadiene versus n-Butane/1,2-Polybutadiene

2005

Solutions of 1,4-polybutadiene (1,4-PB, 98% cis) and of 1,2-polybutadiene (1,2-PB) in n-butane (n-C 4 ) were studied with respect to their vapor pressure and to their demixing into two liquid phases under isochoric conditions within the temperature range from 25 to 75 °C. 1,2-PB mixes homogeneously with n-C 4 at any ratio, in contrast to 1,4-PB, which exhibits a miscibility gap extending from practically pure solvent to approximately 40 wt % polymer. Corresponding to these solubility differences, the vapor pressures for the system n-C 4 /1,4-PB are considerably higher than for n-C 4 /1,2-PB at the same concentration and temperature. The experimental results are modeled accurately and consis…

ChromatographyPolymers and PlasticsIsochoric processSpinodal decompositionVapor pressureOrganic ChemistryThermodynamicsButaneMiscibilityInorganic Chemistrychemistry.chemical_compoundPolybutadienechemistryPhase (matter)Materials ChemistrySolubilityMacromolecules
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Volatile compounds extracted from polypropylene pellets by hot water: influence of the level of the peroxide agents

1992

To improve the quality level of plastic packaging materials, we determined the influence of chemical degradation of polypropylene (PP) upon the amount of volatile components extracted by hot water from PP pellets. Two formulations were analyzed and compared: PP CR (degraded) and PP (not degraded). After Likens-Nickerson's extraction of the pellets and concentration of the extract, an HPLC fractionation was made to collect three fractions of different poiarities: a pentane (A), a dichloromethane (B), and an ether (C) fraction. Fractions (B) and (C) were olfactively evaluated by GC sniffing to be most interesting. Their analysis by GC/MS coupling allowed the identification of different compon…

ChromatographyPolymers and PlasticsNonanal[SDV]Life Sciences [q-bio]010401 analytical chemistryPellets02 engineering and technologyGeneral ChemistryDecanal021001 nanoscience & nanotechnology01 natural sciencesPeroxide0104 chemical sciencesSurfaces Coatings and FilmsPentane[SDV] Life Sciences [q-bio]chemistry.chemical_compoundchemistryMaterials ChemistryPhenols0210 nano-technologyChemical decompositionComputingMilieux_MISCELLANEOUSDichloromethane
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