Search results for "carbon"

showing 10 items of 6057 documents

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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Determination of selected polyaromatic hydrocarbons by gas chromatography–mass spectrometry for the analysis of wood to establish the cause of sinkin…

2014

Abstract The aim of this paper was to establish the cause of sinking of an old wooden vessel by polycyclic aromatic hydrocarbon (PAH) analyses because wood combustion is a source of PAHs. In particular, the molecular PAH patterns generated by each source are like fingerprints and it is possible to determine the processes that generate PAHs by studying their distribution in wood samples. The relative abundance of high molecular weight PAHs, together with the PAH compound ratios and with total index (proposed by us) has demonstrated that samples owe their PAHs in wood archaeological material to a predominant single mode of origin, i.e. combustion processes, therefore we can say that the sinki…

chemistry.chemical_classificationVesselChemistryPolycyclic aromatic hydrocarbonArchaeologicalArchaeologicalVesselFirePAHsFireCombustionSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliAnalytical ChemistryPAHsEnvironmental chemistrypolycyclic compoundsSettore CHIM/01 - Chimica AnaliticaGas chromatography–mass spectrometrySpectroscopyMicrochemical Journal
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Sesquiterpene lactones, waxes and volatile compounds from Artemisia herba-alba subspecies Valentina

1979

Abstract The structures of two sesquiterpene lactones isolated from Artemisia herba-alba subsp. valentina have been determined by spectroscopic methods. One of these was dihydroreynosin, the other was a new compound assigned the name torrentin. The chemical compositions of a wax and a hydrocarbon fraction from the essential oil have also been investigated.

chemistry.chemical_classificationWaxbiologyArtemisia herba-albaFraction (chemistry)Plant ScienceGeneral MedicineHorticultureSubspeciesbiology.organism_classificationSesquiterpeneBiochemistrylaw.inventionchemistry.chemical_compoundHydrocarbonchemistrylawvisual_artBotanyvisual_art.visual_art_mediumArtemisiaOrganic chemistryMolecular BiologyEssential oilPhytochemistry
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Deformation recovery behavior of a solid polymer after tensile yielding

1984

In this work the deformation recovery behavior of an amorphous polymer after large tensile deformation is studied at different temperatures. The effect of three parameters other than temperature has been pointed out in previous works (1–3).

chemistry.chemical_classificationWork (thermodynamics)Materials sciencePolymers and PlasticsGeneral ChemistryPolymerDeformation (meteorology)Amorphous solidchemistryResidual stressvisual_artUltimate tensile strengthMaterials ChemistryStress relaxationvisual_art.visual_art_mediumComposite materialPolycarbonatePolymer Engineering and Science
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Deformation recovery behaviour of a solid polymer after tensile yielding

1987

In this work the deformation recovery behavior of an amorphous polymer after large tensile deformation is studied at different temperatures. The effect of three parameters other than temperature has been pointed out in previous works (1–3). The data here presented indicate that the influence of all parameters, including temperature, on recovery behavior can be related to the residual stress, σ *, at the beginning of recovery test. This suggests to plot the recovery versus time curves, relative to different sets of parameters including temperature, by means of the same normalizing groups which were adopted in (2), thus shifting all curves towards a single master curve.

chemistry.chemical_classificationWork (thermodynamics)Materials sciencePolymers and PlasticsGeneral ChemistryPolymerDeformation (meteorology)Condensed Matter PhysicsAmorphous solidchemistryResidual stressvisual_artUltimate tensile strengthMaterials Chemistryvisual_art.visual_art_mediumPolycarbonateComposite materialPolymer Bulletin
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Precise structural investigation of symmetric diblock copolymer thin films with resonant soft X-ray reflectivity

2013

Symmetric diblock copolymers are known to form lamellar structures in the bulk of an organic thin film. Polymer/polymer and polymer/substrate interfaces play a critical role in this application. Here, we report the investigation of multiple buried interfaces by using a novel technique resonant soft X-ray reflectivity which benefits from enhanced contrast between different polymers near the carbon K-edge. This allows us to obtain a precise interface structure. We also present an alternative method to determine optical constants of polymers by fitting X-ray reflectivity of polymers with known structural parameters at specific soft X-ray energies. This approach is compared with the way of obta…

chemistry.chemical_classification[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Materials sciencechemistry.chemical_elementGeneral ChemistrySubstrate (electronics)PolymerCondensed Matter PhysicsMolecular physicsXANESCrystallographychemistryCopolymerLamellar structure[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Thin filmRefractive indexCarbon[PHYS.COND.CM-SCM]Physics [physics]/Condensed Matter [cond-mat]/Soft Condensed Matter [cond-mat.soft]
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Comparison of the interaction of cobalt bovine carbonic anhydrase II with acetazolamide and methazolamide and the reaction of apoenzyme with cobalt(I…

2003

The metalloenzyme carbonic anhydrase (CA) is an attractive choice for a research-based bioinorganic laboratory course. In this project the interaction of cobalt bovine carbonic anhydrase II (CoBCAII) with acetazolamide and methazolamide and the reaction of apoenzyme with cobalt(II) complexes of acetazolamide and methazolamide is studied by UV-visible spectroscopy. Prior to this spectroscopic study students are given native BCAII, and they prepare apoBCAII and CoBCAII. A major aim is to provide experience in handling metalloproteins and in the study of metal complexes-protein interactions.

chemistry.chemical_classificationbiologyCarbonic anhydrase IIInorganic chemistrychemistry.chemical_elementBioinorganic chemistryBiochemistryEnzymechemistryCarbonic anhydrasemedicineMetalloproteinbiology.proteinMethazolamideAcetazolamideMolecular BiologyCobaltNuclear chemistrymedicine.drugBiochemistry and Molecular Biology Education
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The Mechanism of Action of Carbonic Anhydrase

1990

A survey of the structure-function relationship in the enzyme carbonic anhydrase is presented. The coordination number around the metal ion in derivatives inhibited with some anions is stressed as well as the role of the cavity in determining the coordination number. Inferences on the enzyme-substrate interactions are presented.

chemistry.chemical_classificationbiologyChemistryCoordination numberCombinatorial chemistryMetalEnzymeMechanism of actionvisual_artCarbonic anhydrasemedicinevisual_art.visual_art_mediumbiology.proteinmedicine.symptom
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Use of Mechanistic Information for Adequate Metabolic Design of Genotoxicity Studies and Toxicological Interactions of Drugs and Environmental Chemic…

1995

Microorganisms as well as mammalian cells used for mutagenicity investigations have little or no activities for metabolism of premutagens and precarcinogens, i.e. of compounds ultimately leading to mutations and cancer but first requiring metabolic activation. Therefore, to such cells an exogenous activating system is added, generally the postmitochondrial supernatant fraction of the liver homogenate and a NADPH-generating system (Ames et al. 1976). In this situation enzymes requiring cofactors other than NADP(H) are unlikely to be active. Thus, this metabolic system is rather artificial. Monooxygenases are active in this system. They, for example, convert polycyclic aromatic hydrocarbons t…

chemistry.chemical_classificationbiologyChemistryPolycyclic aromatic hydrocarbonMetabolismPharmacologyMonooxygenasemedicine.disease_causeCofactorEnzymeBiochemistrymedicinebiology.proteinEpoxide hydrolaseGenotoxicityCarcinogen
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Benthic resources are the key to Daphnia middendorffiana survival in a high arctic pond

2011

Summary 1. Shallow arctic lakes and ponds have simple and short food webs, but large uncertainties remain about benthic–pelagic links in these systems. We tested whether organic matter of benthic origin supports zooplankton biomass in a pond in NE Greenland, using stable isotope analysis of carbon and nitrogen in the pond itself and in a 13C-enrichment enclosure experiment. In the latter, we manipulated the carbon isotope signature of benthic algae to enhance its isotopic discrimination from other potential food sources for zooplankton. 2. The cladoceran Daphnia middendorffiana responded to the 13C-enrichment of benthic mats with progressively increasing δ13C values, suggesting benthic feed…

chemistry.chemical_classificationchemistryArcticBenthic zoneEcologyDissolved organic carbonPhytoplanktonEnvironmental sciencePelagic zoneOrganic matterAquatic ScienceZooplanktonIsotope analysisFreshwater Biology
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