Search results for "tyre"

showing 10 items of 586 documents

Potent Aroma Compounds of Two Red Wine Vinegars

2000

Gas chromatography olfactometry (GCO) was used to determine key aroma compounds of two red wine vinegars. Sensory analysis was performed to choose the best neutralization agent of acetic acid (NaOH or MgO) and to test representativeness of four extracts obtained by different methods (dichloromethane extraction, XAD-2, mixture of XAD-2 and XAD-7, and Extrelut resins extraction). Neutralization with NaOH followed by dichloromethane extraction was selected to extract volatile compounds of vinegars. Key odorant compounds were determined by GCO based on detection frequency with 13 people. In the two red wine vinegars, 13 odors were perceived by at least 70% of the panelists, and 8 compounds amon…

Spectrophotometry InfraredAcrylic ResinsWine01 natural sciencesGas Chromatography-Mass SpectrometryButyric acidAcetic acidchemistry.chemical_compound0404 agricultural biotechnology[SDV.IDA]Life Sciences [q-bio]/Food engineeringComputingMilieux_MISCELLANEOUSAromaAcetic AcidDichloromethaneWineChromatographybiology010401 analytical chemistryExtraction (chemistry)04 agricultural and veterinary sciencesGeneral Chemistry[SDV.IDA] Life Sciences [q-bio]/Food engineeringbiology.organism_classification040401 food science0104 chemical scienceschemistryOdorPolystyrenesIon Exchange ResinsGas chromatographyGeneral Agricultural and Biological SciencesJournal of Agricultural and Food Chemistry
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Phase behaviour of poly(vinyl methyl ether)-cross-polystyrene semi-interpenetrating networks

1990

Semi-interpenetrating polymer networks of varying composition are prepared by crosslinking polystyrene containing a small number of maleic anhydride groups (4.8 mol% of MA units) with hexamethylene-diamine (HMDA) in the presence of linear poly(vinyl methyl ether) (PVME). Lightly crosslinked samples are homogeneous at room temperature and show a phase behaviour similar to uncrosslinked blends, i.e. lower critical solution temperature (LCST) behaviour. The influence of crosslinking on the phase behaviour has been studied by small angle light scattering (SALS) and turbidity measurements. The cloud point strongly depends on the heating rate. The presence of the network reduces the stable single…

SpinodalMaterials sciencePolymers and PlasticsScatteringSpinodal decompositionOrganic ChemistryThermodynamicsCondensed Matter PhysicsLower critical solution temperatureLight scatteringCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundchemistryPhase (matter)Temperature jumpPolymer chemistryMaterials ChemistryPolystyreneMakromolekulare Chemie. Macromolecular Symposia
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Epoxide Hydratase: Purification to Apparent Homogeneity as a Specific Probe for the Relative Importance of Epoxides among Other Reactive Metabolites

1977

Aromatic and olefinic compounds can be metabolized by microsomal monooxygenases to epoxides which chemically represent electrophilic species (for reviews, see refs. 1–5). Spontaneous binding of such epoxides to DNA, RNA, and protein has been observed (6–10). Accordingly, such metabolites have been suggested and, in some instances, shown to disturb the normal functions of cells, leading to such effects as mutagenesis (11–14), malignant transformation (15–19), or cell necrosis (20). However, aromatic and olefinic compounds are biotransformed to a vast array of metabolites (cf. refs. 21–27), possibly including a considerable number of reactive metabolites other than epoxides. The relative impo…

StereochemistryMetaboliteEpoxideMutagenmedicine.disease_causechemistry.chemical_compoundBiochemistrychemistryStyrene oxideElectrophilemedicinePyreneDNACyclohexene oxide
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1980

Formation and behaviour of radiation induced free radicals in statistical copolymers from vinyl hydrosulfide and styrene (1:1, 1:4, and 1:10) were investigated by means of ESR spectroscopy. The corresponding homopolymers were also included in these studies. After γ-irradiation of the copolymers at 77 K and subsequent annealing to 293 K it was possible to detect thio radicals. Their relative yields were found to increase with increasing styrene content. Investigations regarding the thermal behaviour of the radiation induced radicals in the copolymers allowed the assumption of two mechanisms responsible for the formation of the thio radicals: First, the formation takes place via ion radicals …

Steric effectsChemistryRadicalThio-Photochemistrylaw.inventionIonStyrenechemistry.chemical_compoundlawPolymer chemistryCopolymerElectron paramagnetic resonanceBenzeneDie Makromolekulare Chemie
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1976

tert-Butoxy radicals were generated by decomposing di-tert-butyl hyponitrite. The relative reactivities of substrates were measured from the ratio of tert-butanol and acetone formed. Polystyrene was found to be less reactive than model compounds. Activation parameters for the hydrogen abstraction reaction for cumene, 3-phenylpentane, and 2,4-diphenylpentane are reported and show small differences for the enthalpy of activation; large negative values for the entropy of activation demonstrate the importance of steric hindrance in the hydrogen abstracting step. 2,3-Diphenylbutane as model compound for head to head links in polystyrene exhibits low reactivity, whereas 2,5-diphenylhexane, a mode…

Steric effectsCumenechemistry.chemical_compoundHyponitriteChemistryDimerRadicalPolymer chemistryReactivity (chemistry)PolystyreneHydrogen atom abstractionDie Makromolekulare Chemie
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Azoxybenzene rearrangement catalyzed by solid acids

2008

Abstract For the first time, the potential of acidic cation-exchange resin (sulfonated polystyrene) to catalyze the Wallach rearrangement of azoxybenzene into 4-hydroxyazobenzene has been proved. This finding reveals an alternative reaction path possible in a heterogeneous process using solid acids and may help to clear some doubts concerning the rearrangement mechanism postulated so far. The resin-induced reaction was found to proceed exclusively in a non-polar medium. Reasonable yield was obtained particularly in isooctane due to favorable distribution of azoxybenzene throughout the resin's matrix. On the contrary, the HY type zeolite did not activate the rearrangement, most probably beca…

Steric effectsHeterogeneous catalysisZeoliteAzo compoundProcess Chemistry and TechnologyDFT calculationsWallach rearrangementHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundchemistryComputational chemistryYield (chemistry)Azoxybenzene rearrangementPolymer chemistryPolystyrenePhysical and Theoretical ChemistryZeoliteSulfonated polystyrene resinJournal of Molecular Catalysis A: Chemical
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ChemInform Abstract: nBuLi-Mediated Hydrophosphination: A Simple Route to Valuable Organophosphorus Compounds.

2010

A straightforward synthesis of homoallyl- and allylphosphanes has been developed using nBuLi-mediated hydrophosphination of conjugated dienes. In all the cases the phosphorus atom of the reacting phosphane attacked the sterically less demanding side of the diene exclusively. In addition, high regioselectivities towards 1,2- or 1,4-addition products were observed depending on the nature of the dienes. This hydrophosphination reaction was extended to a variety of substrates such as styrene derivatives, alkynes and 1,3,5-cycloheptatriene. The structures of three hydrophosphination products were confirmed by X-ray diffraction studies.

Steric effectschemistry.chemical_compoundDienechemistryPhosphorus atomHydrophosphinationGeneral MedicineConjugated systemCombinatorial chemistryStyreneChemInform
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nBuLi-Mediated hydrophosphination: a simple route to valuable organophosphorus compounds

2010

A straightforward synthesis of homoallyl- and allylphosphanes has been developed using nBuLi-mediated hydrophosphination of conjugated dienes. In all the cases the phosphorus atom of the reacting phosphane attacked the sterically less demanding side of the diene exclusively. In addition, high regioselectivities towards 1,2- or 1,4-addition products were observed depending on the nature of the dienes. This hydrophosphination reaction was extended to a variety of substrates such as styrene derivatives, alkynes and 1,3,5-cycloheptatriene. The structures of three hydrophosphination products were confirmed by X-ray diffraction studies.

Steric effectsligand designDieneAlkyneConjugated system010402 general chemistryalkynes01 natural sciencesChemical synthesisStyrenechemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistryhydrophosphinationOrganic chemistryPhysical and Theoretical ChemistryphosphorusComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationalkenes010405 organic chemistryAlkene[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryRegioselectivity0104 chemical scienceschemistry
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Continuous spin fractionation and characterization by size-exclusion chromatography for styrene-butadiene block copolymers.

2005

Abstract Linear and star-shaped styrene–butadiene block copolymers synthesized by anionic polymerization of butadiene and styrene were fractionated by applying a newly developed large-scale fractionation technique, named continuous spin fractionation (CSF). Their molecular weight and polydispersity index ( d  =  M w / M n ) were measured with size-exclusion chromatography and static light scattering. For the linear triblock copolymer a fractionation via temperature variation turned out to be better suited than the usual isothermal procedure. The star-shaped polymer with the d value of 1.33 was fractionated in two CSF steps to get the targeted sample, which has a considerably more uniform st…

Styrene-butadieneChromatographyOrganic ChemistryDispersitySize-exclusion chromatographyGeneral MedicineFractionationBiochemistryAnalytical ChemistryStyreneGel permeation chromatographyMolecular Weightchemistry.chemical_compoundchemistryCopolymerButadienesChromatography GelMolar mass distributionPolystyrenesStyreneJournal of chromatography. A
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Poly(N-isopropylacrylamide)-Modified Styrene-Butadiene Rubber as Thermoresponsive Material

2013

Styrene-butadienePolymers and PlasticsThiol-ene reactionOrganic ChemistryCondensed Matter Physicschemistry.chemical_compoundchemistryNatural rubbervisual_artPolymer chemistryMaterials ChemistryPoly(N-isopropylacrylamide)visual_art.visual_art_mediumOrganic chemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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