Search results for "Plastics"

showing 10 items of 2724 documents

Maghemite polymer nanocomposites with modulated magnetic properties

2007

A method is presented for the production of maghemite polymer nanocomposites with modulated magnetic properties. Magnetic nanocomposites prepared using this method show regular variation in the magnetic blocking temperature from 2 K to 300 K, and variation in the saturation magnetization from 0 to 50 emu g � 1 (Fe2O3). The method is based on the in situ formation of maghemite nanoparticles in nitrogen-base polymer matrixes. The particle size can be varied regularly from 1.5 nm to 16 nm by changing the ratio of iron loading in the polymer and/or the Fe(II)/Fe(III) ratios. The particles are isolated and uniformly distributed within the matrix. The mate

chemistry.chemical_classificationIn situNanocompositeMaterials sciencePolymers and PlasticsPolymer nanocompositeMetals and AlloysMaghemiteNanoparticlePolymerengineering.materialElectronic Optical and Magnetic MaterialsNuclear magnetic resonancechemistryChemical engineeringCeramics and CompositesengineeringParticle sizeActa Materialia
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Progress in Understanding of the Interactions between Functionalized Polyolefins and Organo-Layered Double Hydroxides

2013

The dispersion of organo-layered double hydroxides (O-LDH) in functionalized polyolefins (POs) is investigated. Two different polyethylene matrices (maleic anhydride (MAH) and diethyl maleate functionalized) are tested and a hydrogenated fatty acid modified LDH is used. The attention is focused on evidencing the interaction between the functional groups of the polymer and the O-LDH through FT-IR. Moreover, a combination of solvent fractionation, morphological, and rheological characterizations enables to gain a deeper insight into the structure of these composites. In particular, the formation of bridging bonds between the particles and MAH functionalized macromolecules is assumed, possibly…

chemistry.chemical_classificationIonic clustersPolymers and PlasticsChemistryGeneral Chemical EngineeringLayered double hydroxidesMaleic anhydrideGeneral ChemistryPolymerengineering.materialPolyethylenechemistry.chemical_compoundPolymer chemistrySolvent fractionationengineeringDispersion (chemistry)MacromoleculeMacromolecular Reaction Engineering
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Absorption and desorption of liquid water by a superabsorbent polymer: Effect of polymer in the drying of the soil and the quality of certain plants

2001

In this work, we were interested in the study of the kinetic behavior of the reaction of drying soil representing the Marrakesh region (south of Morocco) in the presence of an superabsorbent polymer. The presence of a polymer in the soil diminished the kinetic drying of the soil, which will have as an application a reduction in water loss in the process of irrigation. The presence of a polymer in the soil enables a complete modification of the kinetic regimes controlling the soil-drying kinetic. We also realized the first study of the behavior of certain selected plants in the melange of a soil and a polymer. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 234–243, 2002

chemistry.chemical_classificationIrrigationAbsorption of waterPolymers and PlasticsGeneral ChemistryPolymerPolyelectrolyteSurfaces Coatings and FilmschemistrySuperabsorbent polymerChemical engineeringDesorptionSoil waterMaterials ChemistryOrganic chemistryAbsorption (chemistry)Journal of Applied Polymer Science
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Absorption and desorption of liquid water by a superabsorbent polyelectrolyte: Role of polymer on the capacity for absorption of a ground

2001

To study the potentialities of a polyelectrolyte superabsorbent for the storage of water, we have studied a ground representative of the area of Haouz (area of Marrakesh, South of Morocco) in the presence of polymer. We sought the optimal proportions allowing the best retention of water by the mixture made up of the polymer and the ground and to prolong the storage period of water in the ground. We have also studied the effect of certain ions and the pH on the capacity for absorption of polymer. These ions can be naturally present in the ground or introduced by the means of manure and pesticides. The presence of polymer in the ground makes it possible to increase the capacity for absorption…

chemistry.chemical_classificationIrrigationAbsorption of waterPolymers and PlasticsInorganic chemistryGeneral ChemistryPolymerPolyelectrolyteSurfaces Coatings and FilmsIonInfiltration (hydrology)chemistryDesorptionMaterials ChemistrymedicineSwellingmedicine.symptomJournal of Applied Polymer Science
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Mechanism of anionic polymerization of methyl methacrylate in the presence of aluminium alkyls

1995

Methyl methacrylate was polymerized with tert-butyl lithium in the presence of triethylaluminium or triisobutylaluminium at 78°C in toluene. As indicated by GPC and MALDI-TOF mass spectrometry, the polymerization is accompanied by side reactions. The lower oligomers were fractionated by distillation and characterised by NMR, FT-IR, UV and electron impact (EI) mass spectrometry. All these data show that part of the polymer chains are carrying exactly one tert-butyl isoprenyl ketone unit. In order to avoid the formation of tert-butyl isoprenyl ketone a molar ratio of Al/Li>2 is necessary.

chemistry.chemical_classificationKetonePolymers and PlasticsChemistryOrganic ChemistryCondensed Matter PhysicsMethacrylateToluenechemistry.chemical_compoundAnionic addition polymerizationTriethylaluminiumPolymerizationPolymer chemistryMaterials ChemistryMethyl methacrylateTriisobutylaluminiumMacromolecular Symposia
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Properties of Hydrophobic Polymer Melts Tethered to the Water Surface As Determined with in Situ X-ray Reflectivity

1997

Insoluble monolayers of hydrophobic polymers with low glass transition temperature (perfluoropolyethers, polyisoprenes) and a single ionic head group (carboxylic acid, sulfonate) have been characterized at the air/water interface via X-ray reflectivity measurements. The films are considerably thicker (30−420 A) than conventional Langmuir monolayers of low molecular weight substances or polymers with surface active repeat units. The thickness is inversely proportional to the area per head group and is in accordance with a model assuming a solvent-free hydrophobic layer of the same density as the bulk material.

chemistry.chemical_classificationLangmuirPolymers and PlasticsOrganic ChemistryIonic bondingPolymerInorganic ChemistryX-ray reflectivityEnd-groupchemistry.chemical_compoundSulfonatechemistryChemical engineeringPolymer chemistryMonolayerMaterials ChemistryGlass transitionMacromolecules
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An Easy Way Towardɛ-Caprolactone Macromonomers by Microwave Irradiation Using Early Lanthanide Halides as Catalysts

2002

Poly(e-caprolactone) macromonomers were synthesized under microwave irradiation from commercial caprolactone, using commercial hydrated lanthanide halides as catalysts. The molecular weight of the polymers was in the range 3 000–5 000. Higher molecular weights (5 000–20 000) and lower polydispersity indices were obtained with THF adducts of the lanthanide halides as catalysts and also by applying longer reaction times or using diethylene glycol as a coupling reagent.

chemistry.chemical_classificationLanthanideMaterials sciencePolymers and PlasticsOrganic ChemistryDispersityDiethylene glycolHalidePolymerMacromonomerRing-opening polymerizationchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCaprolactoneMacromolecular Rapid Communications
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Dragging a Polymer Chain into a Nanotube and Subsequent Release

2008

We present a scaling theory and Monte Carlo (MC) simulation results for a flexible polymer chain slowly dragged by one end into a nanotube. We also describe the situation when the completely confined chain is released and gradually leaves the tube. MC simulations were performed for a self-avoiding lattice model with a biased chain growth algorithm, the pruned-enriched Rosenbluth method. The nanotube is a long channel opened at one end and its diameter $D$ is much smaller than the size of the polymer coil in solution. We analyze the following characteristics as functions of the chain end position $x$ inside the tube: the free energy of confinement, the average end-to-end distance, the averag…

chemistry.chemical_classificationLattice model (finance)NanotubeCritical distanceMaterials scienceStatistical Mechanics (cond-mat.stat-mech)Polymers and PlasticsOrganic ChemistryMonte Carlo methodFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterMolecular physicsInorganic ChemistrychemistryChain (algebraic topology)Phase (matter)Materials ChemistrySoft Condensed Matter (cond-mat.soft)Tube (fluid conveyance)Condensed Matter - Statistical MechanicsMacromolecules
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Tracer diffusion properties of core-shell latex films studied by photoinduced grating relaxation

2007

This article reports the application of the Photo-Induced Grating Relaxation technique (also known as Forced Rayleigh Scattering) to investigate the dynamics of films prepared from structured core–shell latex particles via the transport property of the photochromic tracer molecule Aberchrome 540®. The core–shell particles were prepared with a fluoropolymer core (immiscible and impenetrable to the tracer) and a poly(butyl methacrylate) shell. The incompletely dried films (with residual water) manifest their spatial heterogeneity via non-Fickian behavior (spatial scale- dependent apparent diffusion coefficient). The diffusion data was interpreted using the two-state diffusion model, previousl…

chemistry.chemical_classificationLength scaleMaterials sciencePolymers and PlasticsPolymerStrain hardening exponentCondensed Matter PhysicsFick's laws of diffusionchemistry.chemical_compoundsymbols.namesakechemistryChemical physicsPolymer chemistryMaterials ChemistrysymbolsFluoropolymerEffective diffusion coefficientPhysical and Theoretical ChemistryDiffusion (business)Rayleigh scatteringJournal of Polymer Science Part B: Polymer Physics
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Chemical recycling of polyenaminones by transamination reaction via amino–enaminone polymerisation/depolymerisation

2019

Abstract Novel oligo- and polyenaminones with Mw ∼ 3000 Da were prepared in excellent yields by amino–enaminone ‘click’ polymerisation of 1,3- and 1,4-bis[3-(dimethylamino)acryloyl]arenes with 1,3- and 1,4-phenylenediamine. The obtained oligomers and polymers were depolymerised quantitatively to the starting bis-enaminones and diamines by treatment with excess dimethylamine in ethanol at 50 °C. This simple polymerisation/depolymerisation method allows for a closed-loop recycling of polyenaminone-based materials. UV light absorbance at wavelengths below 470 nm indicates promising optical properties of these polymers.

chemistry.chemical_classificationLight absorbanceEthanolPolymers and PlasticsTransaminationOrganic ChemistryGeneral Physics and Astronomy02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymerizationMaterials Chemistry0210 nano-technologyDimethylamineEuropean Polymer Journal
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