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showing 10 items of 2851 documents

Mode I interlaminar fracture toughness of thin-ply laminates with CNT webs at the crack interface

2019

Abstract Pristine and functionalized carbon nanotube (CNT) webs were introduced at the interlaminar region of two different thin-ply carbon fibre reinforced polymer systems (NTPT 402 prepreg, and TeXtreme/SE84LV). The Mode I interlaminar fracture toughness (ILFT) for the NTPT 402 material was substantially lower. In contrast when SE84LV resin was used, the resistance curves were virtually unchanged and with no depreciation in the steady state value of the ILFT. This demonstrates that a careful choice of the resin is essential to permit the embedding of CNT webs in thin-ply laminates without compromising structural performance and opens a new way towards the development of multifunctional th…

chemistry.chemical_classificationSteady stateMaterials science/dk/atira/pure/subjectarea/asjc/2200/220502 engineering and technologyPolymerCarbon nanotube021001 nanoscience & nanotechnologylaw.inventionA. Thin-ply laminatesC. Interlaminar fracture toughness020303 mechanical engineering & transportsFracture toughness0203 mechanical engineeringchemistrylawCeramics and CompositesB. Carbon nanotube (CNT) webs/dk/atira/pure/subjectarea/asjc/2500/2503Composite material0210 nano-technologyCivil and Structural Engineering
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Discrete bond model (DBM) of sodium silicate glasses derived from XPS, Raman and NMR measurements

1993

In sodium silicate glasses, the fraction of differently bound Si species Q[i] (i = 0−4), depending on the number i of bridging oxygens bound to the quarternary silicon, is a function of stoichiometry and the Na/Si ratio. Sodium silicate glasses were investigated by high resolution X-ray photoelectron spectroscopy. To explain the differences in chemical shifts and linewidths of the O 1s signal of the bridging and the non-bridging oxygen as a function of alkali concentration, and extended glass model was developed. This new model takes into account the influence of the alkali concentration on the Q[i] distribution and on the appearance and concentrations of differently bound bridging oxygens …

chemistry.chemical_classificationStereochemistryChemical shiftBinding energyCondensed Matter PhysicsAlkali metalElectronic Optical and Magnetic Materialssymbols.namesakeCrystallographychemistryX-ray photoelectron spectroscopyChemical bondMaterials ChemistryCeramics and CompositessymbolsRaman spectroscopyInorganic compoundStoichiometryJournal of Non-Crystalline Solids
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The cyclic [N(PiPr2E)2]+ (E = Se, Te) cations: a new class of inorganic ring system.

2006

The two-electron oxidation of [(tmeda)NaN(PiPr2E)2] with iodine produces the cyclic [N(PiPr2E)2]+ (E = Se, Te) cations, which exhibit long E–E bonds in the iodide salts. peerReviewed

chemistry.chemical_classificationStereochemistryIodideMetals and Alloyschemistry.chemical_elementliganditGeneral ChemistryRing (chemistry)IodineMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsdikalkogenoimidodifosfinaatitdichalcogenoimidodiphosphinateschemistryMaterials ChemistryCeramics and CompositesChemical communications (Cambridge, England)
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Sterically controlled self-assembly of tetrahedral M(6)L(4) cages via cationic N-donor ligands.

2014

Tripodal cationic N-donor ligands exhibit sterically controlled self-assembly of tetrahedral M6L4 coordination cages that promote selective anion encapsulation (PF6(-)OTf(-)) in the solid state. The described method is a potential template for stepwise assembly of hetero-ligand coordination cages and polymers.

chemistry.chemical_classificationSteric effectsChemistryMetals and AlloysSolid-stateCationic polymerizationGeneral ChemistryPolymerCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMaterials ChemistryCeramics and CompositesTetrahedronSelf-assemblyta116Chemical communications (Cambridge, England)
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A clickable NHC–Au(i)-complex for the preparation of stimulus-responsive metallopeptide amphiphiles

2018

We report the synthesis of an alkyne functionalised NHC-Au(i)-complex which is conjugated with amphiphilic oligopeptides using a copper(i) catalysed cycloaddition. The resulting Au(i)-metalloamphiphiles are shown to self-assemble into charge-regulated stimulus-responsive supramolecular polymers in water via a weakly cooperative polymerisation mechanism.

chemistry.chemical_classificationStimuli responsive010405 organic chemistryChemistryMetals and AlloysAlkyneGeneral ChemistryConjugated system010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCycloaddition0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSupramolecular polymersPolymerizationAmphiphileMaterials ChemistryCeramics and CompositesClickableChemical Communications
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Enantioselective self-assembly of antiferromagnetic hexacopper(ii) wheels with chiral amino acid oxamates

2013

The Cu(2+)-mediated self-assembly of oxamato-based ligands derived from either the (S)- or (R)-enantiomers of the amino acid valine leads to the formation of two antiferromagnetically coupled homochiral anionic hexacopper(II) wheels in the presence of templating tetramethylammonium countercations.

chemistry.chemical_classificationTetramethylammoniumStereochemistryMagnetic PhenomenaMetals and AlloysEnantioselective synthesisStereoisomerismValineGeneral ChemistryLigandsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmino acidchemistry.chemical_compoundchemistryCoordination ComplexesValineMaterials ChemistryCeramics and CompositesAntiferromagnetismSelf-assemblyCopperChemical Communications
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Computer simulations of undercooled fluids and the glass transition

2000

Abstract Two model studies are presented that attempt to describe the static and dynamic properties of glass-forming fluids via molecular dynamics simulations: The first model is an atomistically realistic model of SiO 2 , the second model provides a coarse-grained description of polymer liquids, i.e., typical `fragile' glassformers, while SiO 2 is the prototype of a `strong glassformer'. For both models, attention is given to the questions as to which range of temperatures are properties in equilibrium, and whether such simulations can help to interpret experiments and/or check theoretical predictions. While in the simulation of SiO 2 using the potential of van Beest, Kramer and van Santen…

chemistry.chemical_classificationThermodynamicsSodium silicatePolymerAtmospheric temperature rangeCondensed Matter PhysicsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMolecular dynamicsMonomerchemistryMaterials ChemistryCeramics and CompositesGlass transitionPolymer meltMacromoleculeJournal of Non-Crystalline Solids
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Processing and Mechanical Properties of Natural Fiber Reinforced Thermoplastic Starch Biocomposites

2007

Natural fiber reinforced starch polymers are processed by compression molding. Potato, sweet potato, and corn starch are used as matrices. Three types of natural fibers, namely sisal, jute, and cabuya, are used in concentrations varying from 2.5 to 12.5% w/w in the composites. Different plasticizers are used for the starch polymers, such as water and glycerol. Mechanical properties are assessed by tensile and impact tests. In both cases, improved mechanical properties are obtained at increasing fiber contents. Tensile strength appears to be markedly improved with the addition of 10% by weight of sisal fibers, while the best results for impact strength are obtained for cabuya fibers.

chemistry.chemical_classificationThermoplasticMaterials scienceStarchfood and beveragesCompression moldingIzod impact strength test02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter Physicschemistry.chemical_compound020401 chemical engineeringchemistryUltimate tensile strengthCeramics and CompositesFiber0204 chemical engineeringComposite material0210 nano-technologycomputerSISALNatural fibercomputer.programming_languageJournal of Thermoplastic Composite Materials
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Time–carbonyl groups equivalence in photo-oxidative aging of virgin/recycled polymer blends

2004

AbstractThe photo-oxidation behaviour of polymers is strongly dependent on the initial amount of carbonyl groups along the chains. The growing use of recycled post-consumer polymers coming from products used outdoors and then photo-oxidised, both pure and blended with the same virgin polymer, gives rise to an unpredictable behaviour of weathering resistance of products made with these materials. The present work shows that the carbonyl group–exposure time curves can be shifted along the time axis to give a single generalised master plot. It is then possible to predict the formation of the new carbonyl groups by knowing only the initial amount of the same carbonyl groups. The same shift fact…

chemistry.chemical_classificationUnpredictable behaviourWork (thermodynamics)Materials sciencePolymers and PlasticsGeneral Chemical EngineeringPolymerShift factorchemistryPHOTO-OXIDATION RECYCLED POLYMERS TIME CARBONYL GROUPS EQUIVALENCE VIRGIN/RECYCLED POLYMER BLENDSMaterials ChemistryCeramics and CompositesPolymer blendComposite materialPlastics, Rubber and Composites
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Corrigendum to “Biomolecule-corona formation confers resistance of bacteria to nanoparticle-induced killing: Implications for the design of improved …

2020

chemistry.chemical_classificationbiologyChemistryBiomoleculeBiophysicsNanoparticleBioengineeringbiology.organism_classificationBiomaterialsCorona (optical phenomenon)Mechanics of MaterialsCeramics and CompositesBiophysicsBacteriaBiomaterials
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