Search results for "tyre"

showing 10 items of 586 documents

Effect of ageing on the morphology and creep and recovery of polymer-modified bitumens

2018

Polymer additives are used to improve the properties of road bitumens including their oxidative resistance. However, their usage as anti-oxidative materials remains relatively unclear. This study aims to investigate the changes in the morphology and the rheological response of polymer modified bitumens used in road pavement construction caused by ageing. An elastomer (radial styrene butadiene styrene, SBS) and a plastomer (ethyl vinyl acetate, EVA) polymer were mixed with one base bitumen at three polymer concentrations. The bitumens were RTFO and PAV aged. The morphology of the bitumens was captured by fluorescence microscopy while the rheological properties were measured by means of the m…

MorphologyStyrene-butadieneMaterials sciencePercent recovery0211 other engineering and technologies02 engineering and technologyElastomerPlastomerchemistry.chemical_compoundRheology021105 building & constructionSettore ICAR/04 - Strade Ferrovie Ed AeroportiGeneral Materials ScienceComposite materialPolymer-modified bitumenCivil and Structural Engineeringchemistry.chemical_classificationMSCRBuilding and ConstructionPolymer021001 nanoscience & nanotechnologyAgeingchemistryCreepMechanics of MaterialsAsphaltHardening (metallurgy)Polymer-modified bitumen Ageing Morphology Percent recovery MSCR0210 nano-technology
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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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Radical Polymerization of Styrene Controlled by Half-Sandwich Mo(III)/Mo(IV) Couples: All Basic Mechanisms Are Possible

2001

Density functional calculations of bond dissociation energies (BDEs) have been used as a guide to the choice of metal system suitable for controlling styrene polymerization by either the stable free radical polymerization (SFRP) or the atom transfer radical polymerization (ATRP) mechanism. In accord with the theoretical prediction, CpMo(eta(4)-C(4)H(6))(CH(2)SiMe(3))(2), 2, is not capable of yielding SFRP of styrene. Still in accord with theoretical prediction, CpMo(eta(4)-C(4)H(6))Cl(2), 1, CpMo(PMe(3))(2)Cl(2), 3, and CpMo(dppe)Cl(2) (dppe = 1,2-bis(diphenylphosphino)ethane), 4, yield controlled styrene polymerization by the SFRP mechanism in the presence of 2,2'-azobisisobutyronitrile (A…

Nitroxide mediated radical polymerizationDispersityRadical polymerizationFree radicals010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisStyreneStyrenesPolymerizationchemistry.chemical_compoundLiving free-radical polymerizationColloid and Surface ChemistryRadical polymerizationPolymer chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryAlkylchemistry.chemical_classification010405 organic chemistryGeneral Chemistry[CHIM.CATA]Chemical Sciences/CatalysisBond-dissociation energyBond cleavage0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymerschemistryPolymerization
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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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Polymerization of an activated ester monomer based on 4-vinylsulfonic acid and its polymer analogous reaction

2011

Homopolymers containing sulfonic ester side groups were synthesized by reversible addition–fragmentation chain transfer (RAFT) polymerization utilizing benzyl dithiobenzoate, cumyl dithiobenzoate, and 4-cyano-4-((thiobenzoyl)sulfanyl)pentanoic acid as chain transfer agents. Likewise diblock copolymers containing poly(styrene), poly(octylstyrene) and poly(pentafluorostyrene) as the second block were synthesized. Additionally, nitroxide mediated polymerization (NMP) was investigated for the synthesis of a homopolymer as well as for a diblock copolymer. Furthermore, the post-polymerization functionalization with various amines to yield the respective sulfonamides was conducted. The conversion …

Nitroxide mediated radical polymerizationPolymers and PlasticsOrganic ChemistryBioengineeringChain transferBiochemistryVinylsulfonic acidStyrenechemistry.chemical_compoundMonomerSulfonatechemistryPolymerizationPolymer chemistryCopolymerPolym. Chem.
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Half-sandwich molybdenum(III) compounds containing diazadiene ligands and their use in the controlled radical polymerization of styrene

2002

Abstract The reaction of CpMoCl2 with diazadiene ligands RNCHCHNR (R2dad) affords the corresponding paramagnetic complexes CpMoCl2(R2dad) (R=Ph, 1; p-Tol, 2; C6H3Pr2i-2,6, 3; and Pri, 4). All compounds have been characterized by EPR spectroscopy and have been investigated by cyclic voltammetry. They display one-electron oxidation and reduction processes, these being reversible or irreversible depending on the nature of R. The irreversibility of the reduction wave is due to a chemical follow-up process which consists of chloride loss from the reduced product. This phenomenon is suppressed in the presence of excess chloride in solution. An X-ray structure of 3 verifies the mononuclear na…

Nitroxide mediated radical polymerizationRadical polymerization010402 general chemistryPhotochemistry01 natural sciencesBiochemistryChlorideStyreneInorganic ChemistryLiving free-radical polymerizationchemistry.chemical_compoundCyclopentadienyl complexPolymer chemistryMaterials Chemistrymedicine[CHIM.COOR]Chemical Sciences/Coordination chemistryCyclopentadienylPhysical and Theoretical ChemistryControlled radical polymerizationMolybdenumDiazadiene ligands010405 organic chemistryChemistryOrganic Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersCobalt-mediated radical polymerizationPolymerizationParamagnetic organometallicsmedicine.drugJournal of Organometallic Chemistry
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How the interplay of different control mechanisms affects the initiator efficiency factor in controlled radical polymerization: An investigation usin…

2007

International audience; Compound CpMoI2(iPr2dad) (iPr2dad = iPrNdouble bondCHsingle bondCHdouble bondNiPr), obtained by halide exchange from CpMoCl2(iPr2dad) and NaI, has been isolated and characterized by EPR spectroscopy, cyclic voltammetry, and X-ray crystallography. Its action as a catalyst in atom transfer radical polymerization (ATRP) and as a spin trap in organometallic radical polymerization (OMRP) of styrene and methyl acrylate (MA) monomers has been investigated and compared with that of the dichloro analogue. Compound CpMoCl2(iPr2dad) catalyzes the ATRP of styrene and MA with low efficiency factors f (as low as 0.37 for MA and ethyl 2-chloropropionate as initiator), while it irre…

Nitroxide mediated radical polymerizationRadical polymerizationAtom transfer010402 general chemistryPhotochemistry01 natural sciencesBiochemistryOne-electron oxidative additionStyreneInorganic Chemistrychemistry.chemical_compoundLiving free-radical polymerizationPolymer chemistryMaterials ChemistryReversible addition−fragmentation chain-transfer polymerization[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryMethyl acrylateControlled radical polymerizationMolybdenum010405 organic chemistryChemistryAtom-transfer radical-polymerizationOrganic Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersCobalt-mediated radical polymerizationInitiator efficiency factor
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