Search results for "Polystyrene"

showing 10 items of 349 documents

UV-stabilisation of polystyrene-based nanocomposites provided by polyhedral oligomeric silsesquioxanes (POSS)

2012

Abstract The photo-ageing behaviour of Polyhedral Oligomeric SilSequioxane (POSS)-polystyrene (PS) nanocomposites has been investigated for the first time. POSS having different inorganic framework and pendant organic groups have been used in the PS nanocomposite preparation and the formulated films were subjected to accelerated weathering. Compared to pristine PS, the POSS-containing PS developed a lower level of carbonyl and hydroxyl groups as a function of the exposure time, indicating a significantly improved resistance of the nanocomposites to photo-degradation. The results suggest that all of the investigated POSS molecules play a protective role and may extend the in-use lifetime of …

NanocompositeMaterials scienceMorphology (linguistics)Polymers and PlasticsPolymeric matrixMolecular silicaPOSS nanofillerCondensed Matter Physicschemistry.chemical_compoundchemistryMechanics of MaterialsPolymer chemistryMaterials ChemistryPhoto-oxidationMoleculePolystyreneDispersion (chemistry)PolystyreneUV-stabilizersPolymer Degradation and Stability
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Injection molding of syndiotactic polystyrene/clay nanocomposites

2006

This study aims at exploring the effect of a commercial organoclay montmorillonite (MMT) on the final properties of syndiotactic polystyrene (sPS) injection-molded samples. To this goal, injection-molded specimens made from neat sPS and commercial MMT modified with various organic compounds were prepared in different molding conditions. Dispersion of clay was attained via melt blending, directly in the injection chamber of the injection-molding machine. The obtained specimens were analyzed by IR spectroscopy, X-ray diffraction, thermogravimetry, and differential thermal analysis, with the aim of elucidating the effect of clay on the microstructures of the samples. Results clearly show that,…

NanocompositeMaterials sciencePolymers and PlasticsGeneral ChemistryMolding (process)Thermogravimetrychemistry.chemical_compoundCrystallinityMontmorillonitechemistryDifferential thermal analysisMaterials ChemistryOrganoclayPolystyreneComposite materialPolymer Engineering & Science
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On the role of multi-functional polyhedral oligomeric silsesquioxane in polystyrene-zinc oxide nanocomposites

2014

Abstract Multi-functional trisilanol phenyl (TSPH) and trisilanol isobutyl (TSIB) polyhedral oligomeric silsesquioxane (POSS) have been used in the formulation of advanced polystyrene (PS)-zinc oxide (ZnO) nanocomposites. The neat matrix and PS/ZnO-based nanocomposites have been characterized through rheological, morphological, mechanical, and dynamic thermo-mechanical analysis. Both TSPH and TSIB are able to improve the dispersion of ZnO into the polystyrene matrix; furthermore, adding TSIB leads to better results because it facilitates better solubility into the PS matrix and interaction/reaction with the ZnO nanopowder. Finally, the optical properties and photo-oxidative resistance of th…

NanocompositeMaterials sciencePolymers and PlasticsnanocompositeGeneral Chemical Engineeringdispersant agentMetals and Alloyschemistry.chemical_elementZincSilsesquioxanechemistry.chemical_compounddispersant agent; nanocomposites; photo-oxidative resistance; POSS; UV shielding; Chemical Engineering (all); Polymers and Plastics; Materials Chemistry; 2506; Metals and AlloysUV shieldingchemistryphoto-oxidative resistancePolymer chemistrynanocompositesMaterials ChemistryChemical Engineering (all)Polystyrene2506POSS
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Chiral helical nanostructures based on amorphous abc-triblock copolymers

1995

So far all lattices of regular microdomain structures reported in the literature, either based on binary AB, ABA or ternary ABC block copolymers, can be described using simple symmetry elements like mirror planes, symmetry centers and rotation axes. The microphase separation in a linear ternary block copolymer consisting of three immiscible components namely polystyrene, polybutadiene and polymethyl methacrylate gives rise to the formation of a chiral supramolecular assembly in which chirality is not defined on a molecular (or macromolecular) level but only by the assembly of the linear triblock copolymer molecules. The polybutadiene (7, 12 wt.-%) phase forms helical strands surrounding the…

NanostructureMaterials sciencePolymers and PlasticsOrganic ChemistryCondensed Matter PhysicsSupramolecular assemblyCrystallographychemistry.chemical_compoundPolybutadienechemistryPolymer chemistryMaterials ChemistryCopolymerLamellar structurePolystyreneChirality (chemistry)Ternary operationMacromolecular Symposia
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Controlled radical polymerization of alkyl acrylates and styrene using a half-sandwich molybdenum(III) complex containing diazadiene ligands

2003

Abstract The half-sandwich molybdenum(III) complex CpMoCl 2 ( i Pr 2 -dad) ( i Pr 2 -dad= i Pr–NCH–CHN– i Pr) proved to be an effective metal catalyst for the controlled radical polymerization of methyl acrylate, butyl acrylate, and styrene. In conjunction with an alkyl iodide [R–I: CH 3 CH(COOEt)I] as an initiator and in the presence or absence of Al(O– i -Pr) 3 as a co-catalyst, the molybdenum-based system gave polymers with narrow molecular weight distributions. The in situ addition of styrene to a macroinitiator of poly(methylacrylate) afforded an AB-type block copolymer.

Nitroxide mediated radical polymerizationPolymers and PlasticsBlock copolymerButyl acrylateRadical polymerizationGeneral Physics and Astronomy010402 general chemistry01 natural sciencesStyrenechemistry.chemical_compoundPolyacrylatePolymer chemistryMaterials ChemistryCopolymer[CHIM.COOR]Chemical Sciences/Coordination chemistryMethyl acrylatePolystyreneAtom transfer radical polymerizationMolybdenum010405 organic chemistryAtom-transfer radical-polymerizationOrganic ChemistrySolution polymerization[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymerschemistryEuropean Polymer Journal
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Half-sandwich Mo(III) complexes with asymmetric diazadiene ligands

2006

The asymmetric 1,4-diazadiene ligands R ∗ N CHCH NR ∗ [R ∗  = ( S )-CH(CH 3 )Ph], R 2 ∗ dad , and 2,2′-bis(4-ethyloxazoline), as-ox, have been used to generate half-sandwich Mo III derivatives by addition to Cp 2 Mo 2 Cl 4 . Ligand R 2 ∗ dad affords a mononuclear, paramagnetic 17-electron product, CpMoCl 2 ( R 2 ∗ dad ) , whereas as-ox leads to the isolation of a dinuclear compound where only one molecule of ligand has been added per two Mo atoms, Cp 2 Mo 2 Cl 4 (as-ox). In the presence of free as-ox, this compound coexists with the paramagnetic mononuclear complex in solution. Both products are capable of controlling the radical polymerization of styrene under typical atom transfer radical…

Nitroxide mediated radical polymerizationRadical polymerizationHalf-sandwich complexesDiazadiene010402 general chemistry01 natural sciencesMedicinal chemistryStyreneInorganic Chemistrychemistry.chemical_compoundTacticityPolymer chemistryMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryPolystyreneAtom transfer radical polymerizationMolybdenum010405 organic chemistryLigandAtom-transfer radical-polymerization[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymerschemistryPolystyreneInorganica Chimica Acta
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Wormlike Polystyrene Brushes in Thin Films

1997

Mono- and multilayer films were prepared on mica by solution casting of a high molecular weight polymacromonomer, i.e., a polymethacrylate of about 1000 repeating units each of which was substituted by a polystyrene chain with a molecular weight of about 5000 Da. The films were studied by tapping scanning force microscopy. The material showed a remarkable preference for forming well-defined monolayers of a thickness of 6.5 ± 0.2 nm consistent with the hard core diameter of the collapsed cylindrical brush molecules. When the films were probed with high normal force, the single molecules were observed to organize in a dense nematic-like packing as expected for inherently stiff molecules. In o…

Normal forceMaterials scienceSurfaces and InterfacesSubstrate (electronics)Condensed Matter PhysicsCastingchemistry.chemical_compoundchemistryMonolayerPolymer chemistryElectrochemistryMoleculeGeneral Materials SciencePolystyreneMicaComposite materialThin filmSpectroscopyLangmuir
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Optical experiments on a crystallizing hard-sphere–polymer mixture at coexistence

2010

We report on the crystallization kinetics in an entropically attractive colloidal system using a combination of time resolved scattering methods and microscopy. Hard sphere particles are polystyrene microgels swollen in a good solvent (radius a=380nm, starting volume fraction 0.534) with the short ranged attractions induced by the presence of short polymer chains (radius of gyration rg = 3nm, starting volume fraction 0.0224). After crystallization, stacking faulted face centred cubic crystals coexist with about 5% of melt remaining in the grain boundaries. From the Bragg scattering signal we infer the amount of crystalline material, the average crystallite size and the number density of cry…

Optics and PhotonicsOsmosisMaterials sciencePolymersBiophysicsFOS: Physical sciencesCondensed Matter - Soft Condensed Matterlaw.inventionOpticslawPressureScattering RadiationCrystallizationMicroscopyCondensed matter physicsScatteringbusiness.industryBragg's lawEquipment DesignCondensed Matter::Soft Condensed MatterKineticsVolume fractionRadius of gyrationPolystyrenesSoft Condensed Matter (cond-mat.soft)Grain boundaryCrystalliteSmall-angle scatteringCrystallizationbusinessGelsAlgorithmsPhysical Review E
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The impact of growth history and flagellation on the adhesion of variousListeria monocytogenesstrains to polystyrene

2009

International audience; The contribution of growth history and flagella to adhesion of Listeria monocytogenes was analysed. An in-frame deletion on the flagellin encoding gene (flaA) was performed in L. monocytogenes EGD-e to compare its adhesion ability with the parental strain, after cultivation at various pH values and temperatures. The pH, as well as the temperature, affected the adhesion of L. monocytogenes EGD-e. In addition, the adhesion of L. monocytogenes EGD-e was reduced in energy-depressed cells. Conversely, the physicochemical bacterial surface characteristics affected by growth history did not influence the adhesion. Adhesion variations observed among environmental and clinica…

PHGram-positive bacteriaImmunologyMutantFlagellummedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiologyBacterial AdhesionMicrobiology03 medical and health sciencesADHERENCEListeria monocytogenesGeneticsmedicineHumansListeriosisMolecular Biology030304 developmental biology2. Zero hunger0303 health sciencesbiologyStrain (chemistry)LISTERIA MONOCYTOGENES030306 microbiologyTemperatureFLAGELLINEGeneral MedicineAdhesionHydrogen-Ion Concentrationbiology.organism_classificationCulture Media[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyFlagella13. Climate actionbiology.proteinPolystyrenesFlagellinBacteriaFlagellinCanadian Journal of Microbiology
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Resource or waste? A perspective of plastics degradation in soil with a focus on end-of-life options.

2018

‘Capable-of-being-shaped’ synthetic compounds are prevailing today over horn, bone, leather, wood, stone, metal, glass, or ceramic in products that were previously left to natural materials. Plastic is, in fact, economical, simple, adaptable, and waterproof. Also, it is durable and resilient to natural degradation (although microbial species capable of degrading plastics do exist). In becoming a waste, plastic accumulation adversely affects ecosystems. The majority of plastic debris pollutes waters, accumulating in oceans. And, the behaviour and the quantity of plastic, which has become waste, are rather well documented in the water, in fact. This review collects existing information on pla…

PLA polylactic acidPS polystyreneETS European Emissions Trading schemePOM polyoxymethyleneHMC heat melt compactor technology02 engineering and technology010501 environmental sciencesNHV net habitable volumeLDPE low-density polyethylene01 natural sciencesPC polycarbonateResin identification codeLCP liquid crystal polymerslcsh:Social sciences (General)PAC pro-oxidant additive containingPET polyethylene terephthalateEPR Extended Producers ResponsibilityMultidisciplinaryWaste managementNatural materials021001 nanoscience & nanotechnologyPU or PUR polyurethaneSettore AGR/02 - Agronomia E Coltivazioni ErbaceeEPS expandable polystyreneRIC resin identification codeSettore AGR/14 - PedologiaPVDF polydifluoroethylenelcsh:H1-990210 nano-technologyBiogeoscienceGPPS Polystyrene (General Purpose)PVC polyvinyl chlorideResource (biology)Polymethyl methacrylatePA polyamidePBT polybutylene terephthalatePSU polyarylsulfonePTFE polytetrafluoroethylenePMMA polymethyl methacrylatePHA polyhydroxyalkanoateMicrobiologyPEEK polyaryletheretherketoneArticleEnvironmental scienceEnvironmental science Biogeoscience Industry MicrobiologyPPA polyphthalamideTPE thermoplastic polyester elastomerNatural degradationIndustryPPS polyphenylene sulphidelcsh:Science (General)ABS acrylonitrile-butadiene-styrene0105 earth and related environmental sciencesbusiness.industryPP polypropyleneHDPE high-density polyethyleneBPA bisphenol AHBCD hexabromocyclododecaneFuture studyAgricultureDOM dissolved organic matterDegradation (geology)Environmental sciencebusinesslcsh:Q1-390Heliyon
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