Search results for "polymerization kinetic"

showing 4 items of 4 documents

Copolymerization of VDF and HFP in Supercritical Carbon Dioxide: Experimental Analysis of the Reaction Loci

2010

Free radical copolymerization reactions of vinylidene fluoride (VDF) and hexafluoropropylene (HFP) were carried out in supercritical carbon dioxide at T=50 °C. When ammonium carboxylate perfluoropolyether surfactants were used, the formation of polymer particles was observed provided that HFP mole fraction in the feed was not larger than 0.30. Under these conditions, the effect of the total interphase area of the polymer phase, Ap, on the product propertieswas investigated by comparing experiments with largely different amounts of stabilizer, i.e., ranging from precipitation (smaller Ap) to dispersion (larger Ap) polymerization systems. We found that the copolymer molecular weight distribut…

Dispersion polymerizationSupercritical carbon dioxidePolymers and PlasticsOrganic ChemistryRadical polymerizationsupercritical carbon dioxide fluoropolymers free radical polymerization polymerization kineticsSettore ING-IND/27 - Chimica Industriale E TecnologicaInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryCarbon dioxideMaterials ChemistryCopolymerCarboxylateHexafluoropropyleneFluoride
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Sol–gel material as a support of organometallic catalyst for ethylene polymerization

2008

Abstract The sol–gel procedure was applied to obtain powdery materials with different structures and morphology. It was possible to produce almost non-porous silica powder, with an extremely low surface area (ca. 4 m 2 /g) and very high uniformity of spherical particles as well as materials with various uniformity of particles and different porosity, most likely associated with increasing pore volume. Dependent on the properties of the carrier, the resulting supported vanadium catalysts (VOCl 3 /AlEt 2 Cl) showed significant differences concerning activity and stability. It was confirmed that improved hydrophobicity of the carrier’s surface may be useful and improve the activity of the syst…

Ethylene polymerizationPolymers and PlasticsOrganic ChemistrySupported catalystsGeneral Physics and AstronomyVanadiumchemistry.chemical_elementSilicaPolyethyleneSol–gelChlorideCatalysischemistry.chemical_compoundReaction rate constantchemistryPolymerizationChemical engineeringPolymer chemistryMaterials ChemistrymedicinePorosityPolymerization kineticmedicine.drugSol-gelEuropean Polymer Journal
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Polymerisationskinetische und konduktometrische messungen an polystyrylionenpaaren in einem größeren temperaturbereich

1974

Messungen der Bruttogeschwindigkeitskonstante von Polystyryl-Natrium in 3-Methyltetrahydrofuran (3-Me-THF) in Abhangigkeit von der Konzentration der “lebenden” Kettenenden und der Natriumionen ergeben, das die Monomeraddition wie in anderen polaren Losungsmitteln nach einem Mehrwegmechanismus erfolgt. Der Ubergang vom Kontakt- zum solvatgetrennten Ionenpaar wird in einem Temperaturbereich von — 110 bis +85°CC mit Hilfe kinetischer Messungen im Stromungsrohr und durch Leitf ahigkeitsmessungen verfolgt. Analog zu entsprechenden Untersuchungen in Tetrahydrofuran kann dabei die Polymerisation uber jeweils eine Art von Ionenpaaren fast vollstandig isoliert beobachtet werden. Die thermodynamische…

chemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationPolymerization kineticsKineticsPolymer chemistryConductanceAtmospheric temperature rangeTetrahydrofuranStyreneDie Makromolekulare Chemie
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Effect of hydrogen on the ethylene polymerization process over Ziegler–Natta catalysts supported on MgCl2(THF)2. II. Kinetic studies

2001

This article reports on a study of the effects of hydrogen on the activity of vanadium and titanium catalysts supported on MgCl2(THF)2 in ethylene polymerization. It was found that hydrogen did not change the stable nature of the active sites and the polydispersity index of the polyethylene obtained. The propagation rate, expressed as kp, was found to be independent of the presence and concentration of hydrogen, indicating that this reacting agent does not modify the reactivity of the active sites. However, the presence of hydrogen in the polymerization medium is responsible for partial deactivation of the active sites just before polymerization is initiated.

polymerization kineticethylene polymerizatiovanadium and titanium catalystshydrogencatalyst activityJournal of Applied Polymer Science
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