Search results for "styrene"

showing 10 items of 561 documents

ChemInform Abstract: Covalently Supported Ionic Liquid Phases: An Advanced Class of Recyclable Catalytic Systems

2016

In this review, the most recent advances in the synthesis and catalytic applications of covalently supported ionic liquid (IL) phases will be discussed. This class of recyclable catalytic materials is based on the covalent attachment of several types of ammonium salts, usually imidazolium, but also thiazolium, triazolium, and pyrrolidinium salts, on the surface of different supports, for example, silica, periodic mesoporous organosilica, polystyrene, magnetic-based materials, carbon nanotubes (NTs), halloysite NTs, polyhedral oligomeric silsesquioxane (POSS), and fullerenes. Moreover, poly(ionic liquid) materials, in which the IL-based structure also acts as a support, will be considered. T…

FullereneGeneral MedicineCarbon nanotubeSilsesquioxaneCatalysislaw.inventionchemistry.chemical_compoundMesoporous organosilicachemistryChemical engineeringCovalent bondlawIonic liquidPolystyreneChemInform
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Solution properties of polyelectrolytes. III. Effect of sodium polystyrene sulfonate concentration on viscometric and size exclusion chromatographic …

1988

The effect of sodium polystyrene sulfonate concentration on the shape of its molecules in aqueous solution at different NaNO3 ionic strengths has been analyzed by viscometry and size-exclusion chromatography (s.e.c). An equation has been developed which predicts the intrinsic viscosity, [η] p.cp.cs, at finite concentration of both polyion (cp) and electrolyte (cs). The experimental results obtained by both techniques can be accounted for in terms of the theory. Several factors involved in the elution mechanism have been considered and the variation of the slopes of s.e.c. calibration curves with cp and cs has been discussed in terms of polyion conformation changes.

Gel permeation chromatographyChromatographyAqueous solutionChemistryIonic strengthIntrinsic viscositySize-exclusion chromatographyGeneral EngineeringGeneral Materials ScienceElectrolyteSodium Polystyrene SulfonatePolyelectrolyteBritish Polymer Journal
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Solution properties of polyelectrolytes. I. Exclusion chromatography of sodium polystyrene sulphonate in salt-free water as eluent

1987

The effect of concentration of sodium polystyrene sulphonate on the elution volume in exclusion chromatography has been investigated using salt-free water as eluent. A non-linear increase in the elution volume has been observed with increasing injected sample concentration. Concentration-dependent calibrations have been obtained which approach the universal calibration for uncharged polymers (dextrans) as polyelectrolyte concentration increases. The separation mechanisms are interpreted in terms of electrostatic and hydrodynamic interactions. A semi-empirical model is proposed to predict concentration effects of linear polyions in exclusion chromatography and good agreement has been found b…

Gel permeation chromatographychemistry.chemical_classificationViscosityColumn chromatographyChromatographyChemistryElutionSize-exclusion chromatographyGeneral EngineeringGeneral Materials SciencePolymerSodium polystyrene sulphonatePolyelectrolyteBritish Polymer Journal
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Zur Gelpermeationschromatographie in organischen Lösungsmitteln

1965

Die Gelpermeationschromatographie hat sich vor allem mittels der Sephadexgele fur die Trennung polymerhomologer wasserloslicher Makromolekule als sehr erfolgreich erwiesen. Die Trennung nur in organischen Losungsmitteln loslicher Polymerer ist erst in jungster Zeit gelungen, wobei vernetzte Polystyrol-, Polymethacrylat- und Dextranderivatgele benutzt werden. Der Mechanismus dieses chromatographischen Prozesses wird untersucht. Ein Vergleich dieses Vorganges, bei dem das Polymere nur in einer Phase vorliegt, mit den klassischen Methoden, die mit Auftrennung in zwei Phasen arbeiten, wird durchgefuhrt. Insbesondere werden die Methoden der Dreiecks-Fallungsfraktionierung, der Kolonnentechnik mi…

Gel permeation chromatographychemistry.chemical_classificationchemistry.chemical_compoundChemistryElutionGeneral Chemical EngineeringPolymer chemistryDextran DerivativesPolymerPolystyreneFractionationGeneral expressionSephadex gelsBerichte der Bunsengesellschaft für physikalische Chemie
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Disproportionierung und Kombination als Abbruchsmechanismen bei der radikalischen Polymerisation von Styrol, 2. Analyse der temperaturabhängigkeiten

1975

Styrol wurde in Substanz mit 14C-markiertem 2,2′-Azoisobutyronitril im Temperatur-bereich von 30 bis 80°C polymerisiert. Aus der Polymerisationsgeschwindigkeit und der Anzahl der radioaktiven Endgruppen im Polymeren wurden die Effektivitat des Starters f und die Verhaltnisse der Geschwindigkeitskonstanten fur Wachstum, Abbruch und Start k/ka und ka, PR/(kwkst) berechnet. Die Bestimmung der Molekulargewichtsverteilungen mit Hilfe der Gelpermeationschromatographie ermoglichte es, die Ubertragungskonstante CM und das Verhaltnis ka, disp/ka, comb zu berechnen. Die Temperaturabhangigkeiten der Geschwindigkeitskonstanten erwiesen sich als physikalisch sinnvoll. Styrene was bulk polymerised by ini…

Gel permeation chromatographychemistry.chemical_compoundReaction rate constantchemistryPolymerizationTransfer constantPolymer chemistryAtmospheric temperature rangeStyreneDie Makromolekulare Chemie
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Disproportionierung und kombination als abbruchmechanismen bei der radikalischen polymerisation von styrol, 1.Versuche mit 14C-markierten 2,2′-azoiso…

1975

Die Substanzpolymerisation von Styrol mit 14C-markiertem 2,2′-Azoisobutyronitril (AIBN) wurde bei 52°C experimentell untersucht. Die Polymerisation wurde dilatometrisch verfolgt, die Molekulargewichte der entstandenen Polymeren viskosimetrisch ermit-telt, der Gewichtsbruch der einkettigen Molekule gelchromatographisch bestimmt und die Anzahl der markierten Endgruppen ausgezahlt. Die eingehende kinetische Analyse erhartet die neueren Erkenntnisse uber den Abbruchmechanismus. Danach liegt bei der Polymerisation von Styrol neben der Kombination auch Disproportionierung vor. Bulk polymerisation of styrene initiated by 14C-labelled 2,2′-azoisobutyronitrile (AIBN) was studied at 52°C. The polymer…

Gel permeation chromatographychemistry.chemical_compoundchemistryKinetic analysisPolymer chemistryStyreneDie Makromolekulare Chemie
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Transesterification of rapeseed oil over acid resins promoted by supercritical carbon dioxide

2011

The methanolysis of rapeseed oil catalyzed by commercial styrene-divinylbenzene macroporous acid resins was performed in a batch reactor at 100-140 °C and 10-46 MPa to study the effect of supercritical carbon dioxide (scCO2) on the performances of the process. Reaction temperatures of 120-140 °C were necessary to obtain high enough yields of fatty acid methyl esters. Upon addition of scCO2 faster transesterification kinetics was obtained also at the lowest investigated operating pressure (10-11 MPa), working in two fluid phase systems. Experiments performed changing the reaction time indicated that most of the esters were formed during the first 3 h. When the pressure was increased at 38-46…

General Chemical EngineeringMethanolysiKineticsBatch reactorOperating pressurePolymeric acidHeterogeneous catalysisCatalysiCatalysisHeterogeneous catalysiIon exchange resinSupercritical carbon dioxideOrganic chemistryFatty acid methyl esterRapeseed oilEsterPhysical and Theoretical ChemistryVegetable oils Supercritical fluid extractionIon-exchange resinStyreneReaction systemReaction timeBiodieselFluid phasiTwo-fluid Batch reactorSupercritical carbon dioxideEsterificationChemistryReaction kineticTransesterificationSettore ING-IND/27 - Chimica Industriale E TecnologicaFatty acidCondensed Matter PhysicsPhase behaviourTransesterificationCarbon dioxideReaction temperatureMacroporouStyrene-divinylbenzeneBiodieselEnhancement effectIon exchangeThe Journal of Supercritical Fluids
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Flavobacterium columnare colony types: connection to adhesion and virulence?

2008

Four different colony morphologies were produced by Flavobacterium columnare strains on Shieh agar plate cultures: rhizoid and flat (type 1), non-rhizoid and hard (type 2), round and soft (type 3), and irregularly shaped and soft (type 4). Colonies produced on AO agar differed from these to some extent. The colony types formed on Shieh agar were studied according to molecular characteristics [Amplified Fragment Length Polymorphism (AFLP), Automated Ribosomal Intergenic Spacer Analysis (ARISA), and whole cell protein SDS-PAGE profiles], virulence on rainbow trout fingerlings, and adhesion on polystyrene and fish gills. There were no molecular differences between colony types within one strai…

Gillsfood.ingredientRibosomal Intergenic Spacer analysisVirulenceBiologyMicrobiologyFlavobacteriumVirulence factorBacterial AdhesionMicrobiologyAgar plateFish DiseasesfoodBacterial ProteinsFlavobacteriaceae InfectionsDNA Ribosomal SpacerAgarAnimalsPhase variationVirulencebiology.organism_classificationCulture MediaAgarInfectious DiseasesOncorhynchus mykissFlavobacterium columnarePolystyrenesElectrophoresis Polyacrylamide GelFlavobacteriumPolymorphism Restriction Fragment LengthMicrobial pathogenesis
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New Photosensitive Polymers:  Synthesis and Free Radical Polymerization of Oxypyridinium and Oxyisoquinolinium Functionalized Methacrylate and Styren…

2002

Polymerizable hydroxypyridinium and hydroxyisoquinolinium salts 1a−4a, 2d, and 3d have been prepared from vinylbenzyl chloride or glycidyl methacrylate and 3-hydroxypyridine (2), 4- or 5-hydroxyisoquinoline (1, 3), and 8-hydroxyquinoline (4). Radical homo- and copolymerization with styrene or methyl methacrylate of the salts 1a−3a, 2d, and 3d produced (co)polymers 1e, 2e, 2f, 3f, 1g, 2g, 2h, and 3h. The photosensitive dipolar oxypyridinium or oxyisochinolinium betaine structures were generated in solutions with triethylamine from the low molecular weight and polymeric salt precursors. For the model compounds 1b−4b and (co)polymers 1e, 2e, 2f, 3f, 1g, 2g, 2h, and 3h, the degradation of the l…

Glycidyl methacrylatePolymers and PlasticsOrganic ChemistryRadical polymerizationPhotochemistryMethacrylatePolyelectrolyteStyreneInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerMethyl methacrylateTriethylamineMacromolecules
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Spectrum of styrene-induced DNA adducts: the relationship to other biomarkers and prospects in human biomonitoring.

2002

Styrene is an important industrial chemical that has shown genotoxicity in many toxicology assays. This is believed to be related to the DNA-binding properties of styrene-7,8-oxide (SO), a major metabolite of styrene. In this review, we have summarized knowledge on various aspects of styrene genotoxicity, especially in order to understand the formation and removal of primary DNA lesions, and the usefulness of biomarkers for risk assessment. Biological significances of specific DNA adducts and their role in the cascade of genotoxic events are discussed. Links between markers of external and internal exposure are evaluated, as well as metabolic aspects leading to the formation of DNA adducts …

Health Toxicology and MutagenesisMetabolitePopulation10050 Institute of Pharmacology and Toxicology610 Medicine & healthBiologyIn Vitro Techniquesmedicine.disease_causeRisk AssessmentStyrenechemistry.chemical_compoundDNA Adducts1311 GeneticsOccupational ExposureBiomonitoring2307 Health Toxicology and MutagenesisGeneticsmedicineAnimalsHumanseducationStyreneGeneticseducation.field_of_studyPrimary (chemistry)Binding SitesDNAchemistryBiochemistry570 Life sciences; biologyEpoxy CompoundsXenobioticGenotoxicityDNABiomarkersEnvironmental MonitoringMutagensMutation research
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