Search results for "polymerization"

showing 10 items of 1689 documents

The effect of prepolymerization of a titanium catalyst on its deactivation in propylene polymerization

1997

Propylene polymerization rate was investigated in the presence of anunsupported titanium catalyst (TiCl3) that had been modified with a Lewis base (di-n-butyl ether) and activated (precat), or not activated (cat), by being used in a suspension prepolymerization (70°C, 0.6 MPa) of an identical monomer. The initial polymerization rate was higher with the precat than with the cat catalyst. Prepolymerization was also found to enhance the kinetic stability of catalyst's active sites, presumably by reason of the prepolymerization-induced modification of catalyst's morphology. Deactivation rate constants were evaluated for the active sites of either catalyst examined.

Materials sciencePolymers and PlasticsChemical engineeringPolymerizationGeneral Chemical EngineeringMaterials ChemistryCatalysisA titanium
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Studies of alumina as a support of titanium catalyst for low-pressure ethylene polymerization

1986

The effect of alumina treatment with aqueous solutions of hydrochloric acid and ammonium fluoride as well as temperature of its calcination on the activity of Al-Ti/Al2O3 supported organometallic catalyst for ethylene polymerization has been studied. The dependence between the spe­cific surface area of the support and both the kind and concentration of the modifying agent, concentration of OH-groups on Its surface and concentration of active centres with various activities is discussed with reference to the activity of the supported Al-Ti/Al2O3 catalyst. It was demonstrated that there is no simple relationship between the concentration of OH-groups on the support and the activity of the Ti-…

Materials sciencePolymers and PlasticsChemical engineeringchemistryEthylene polymerizationGeneral Chemical EngineeringMaterials Chemistrychemistry.chemical_elementTitaniumCatalysisPolimery
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Study of methyl methacrylate polymerization in the presence of rubbers

2001

Grafting of poly(methylmethacrylate) onto various unsaturated rubbers is described. The grafting is achieved through thermally initiated methylmethacrylate in-situ polymerization. The main features of the polymerization process, i.e. conversion vs. time, grafting to rubber and gel percentage, have been investigated. The chemical structure of the rubber influences the process: rubber with pendant unsaturations gives rise to higher level of grafting.

Materials sciencePolymers and PlasticsChemical structureOrganic ChemistryKineticstechnology industry and agricultureGeneral Physics and AstronomyGraftingcomplex mixturesbody regionschemistry.chemical_compoundsurgical procedures operativechemistryPolymerizationNatural rubbervisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumMethyl methacrylateIn situ polymerizationNitrile rubberpsychological phenomena and processesEuropean Polymer Journal
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Hyperbranched poly(glycolide) copolymers with glycerol branching points via ring-opening copolymerization

2015

Abstract Sn(Oct) 2 -catalyzed synthesis of hyperbranched poly(glycolide) copolymers with glycerol branching points in the backbone is possible via ring-opening multi-branching copolymerization (ROMBP) of glycolide and 5HDON (5-hydroxymethyl-1,4-dioxan-2-one). Using this strategy, well-defined and soluble branched polyesters with apparent molecular weights (M n ) in the range of 1300–2000 g mol −1 and varying comonomer content (5HDON/glycolide = 30:70–70:30) were obtained. 2D NMR spectroscopy, thermal analysis and MALDI-TOF mass spectrometry confirmed the successful incorporation of both monomers and the resulting branched structure. Multiple end group functionality offers the possibility fo…

Materials sciencePolymers and PlasticsComonomerOrganic ChemistryBiodegradable polymerRing-opening polymerizationPolyesterchemistry.chemical_compoundEnd-groupMonomerchemistryPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryTwo-dimensional nuclear magnetic resonance spectroscopyPolymer
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Surface characterization of functional poly(diacetylene) and poly(butadiene) mono- and multilayers

1982

The surface properties of Langmuir-Blodgett mono- and multilayers of a variety of amphiphilic poly(diacetylene)s and poly(butadiene)s were investigated by contact angle, streaming potentialζ, ellipsometry, and X-ray photoelectron spectroscopic (XPS) measurements. Captive air and octane angles varied between approximately 60° and 105° for hydrophobicx-layers and 31° to 46° for hydrophilic surfaces depending on the particular head group, whereas advancing angles determined via the vertical plate method are considerably higher. Negative streaming potentials were obtained for all surfaces. Positively charged monolayers yielded less negativeζ- potential values (−28 mV) than negatively charged (−…

Materials sciencePolymers and PlasticsDiacetyleneAnalytical chemistryStreaming currentContact anglechemistry.chemical_compoundColloid and Surface ChemistryX-ray photoelectron spectroscopyPolymerizationchemistryEllipsometryMonolayerMaterials ChemistryPhysical and Theoretical ChemistryOctaneColloid and Polymer Science
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Diene/polar monomer copolymers, compatibilisers for polar/non-polar polymer blends. A controlled block copolymerisation with a single-site component …

2002

A well-controlled two-step process, the polymerisation of isoprene or isoprene/hex-1-ene copolymerisation followed by e-caprolactone polymerisation, affords trans-polyisoprene or (trans-polyisoprene/hex-1-ene copolymer)–poly(e-caprolactone) diblocks of various lengths. The single component initiator is an allylsamarocene compound. An atomic force microscopy study shows that these copolymers are efficient compatibilisers for poly(e-caprolactone) and polyisoprene blends. Poly(e-caprolactone) chain growth from Sm–polyisoprene chain.

Materials sciencePolymers and PlasticsDieneOrganic ChemistryCompatibilizationCondensed Matter Physicschemistry.chemical_compoundMonomerchemistryPolymerizationPolycaprolactonePolymer chemistryMaterials ChemistryCopolymerPolymer blendPhysical and Theoretical ChemistryIsopreneMacromolecular Chemistry and Physics
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Synthesis and NMR characterization of new poly(ethoxyalkyl) maleates

1994

Polymerizable surfactants derived from maleic anhydride have been synthesized. The hydrophilic part is obtained by a controlled ethylene oxide polymerization according to a new heterogeneous catalytic process. Some maleates derivatives have been obtained and fully characterized by 1H and 13C NMR. Their cmc were also measured. Some of them have been engaged in styrene emulsion polymerization in which monodisperse latex particles have been produced.

Materials sciencePolymers and PlasticsEthylene oxideDispersitytechnology industry and agricultureMaleic anhydrideEmulsion polymerizationmacromolecular substancesGeneral ChemistryCondensed Matter PhysicsRing-opening polymerizationStyrenechemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerPolymer Bulletin
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Branched Acid-Degradable, Biocompatible Polyether Copolymers via Anionic Ring-Opening Polymerization Using an Epoxide Inimer

2022

The introduction of acid-degradable acetal moieties into a hyperbranched polyether backbone has been achieved by the design of a novel epoxide-based degradable inimer. This new monomer, namely, 1-(glycidyloxy)ethyl ethylene glycol ether (GEGE), has been copolymerized in the anionic ring-opening polymerization (AROP) with ethylene oxide (EO) or glycidol (G), respectively, yielding branched polyethers, that is, P(EO-co-GEGE) and P(G-co-GEGE), that possess an adjustable amount of acid-cleavable acetal units. In addition, a novel class of multiarm star copolymers P(G-co-GEGE-g-EO) with acid-labile polyether core and PEG side chains was synthesized by using the P(G-co-GEGE) copolymers as multifu…

Materials sciencePolymers and PlasticsEthylene oxideOrganic ChemistryGlycidolEpoxideRing-opening polymerizationInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryEthylene glycolACS Macro Letters
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The poly(propylene oxide-co-ethylene oxide) gradient is controlled by the polymerization method: determination of reactivity ratios by direct compari…

2019

An investigation of the highly relevant copolymerization of ethylene oxide (EO) and propylene oxide (PO) by in situ1H NMR spectroscopy shows striking differences in the copolymerization kinetics, depending on the polymerization method. Examination of the EO/PO copolymerization kinetics using iBu3Al for the monomer-activated anionic ring opening polymerization (AROP) confirmed a strong monomer gradient of the microstructure (rEO = 6.4, rPO = 0.16) in contrast to the known weak gradient in the conventional AROP (rEO = 2.8, rPO = 0.25). The first study via in situ1H-NMR kinetics of the copolymerization of PO and EO under heterogeneous double metal cyanide (DMC) catalysis, a method that produce…

Materials sciencePolymers and PlasticsEthylene oxideOrganic ChemistryKineticsBioengineering02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryRing-opening polymerization0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPolymerizationCopolymerPhysical chemistryReactivity (chemistry)Propylene oxide0210 nano-technologyPolymer Chemistry
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Submicron structured polymethyl methacrylate/acrylonitrile-butadiene rubber blends obtained via gamma radiation induced ?in situ? polymerization

2004

The morphology and properties of PMMA/rubber blends, obtained through gamma radiation induced “in situ” polymerization of methyl methacrylate (MMA) in the presence of small quantities of an acrylonitrile–butadiene based rubber (ABN), are presented. Different systems have been obtained by irradiating at a fixed irradiation dose rate and temperature, varying the integrated dose. All the blends obtained were characterized with respect to their melt state and solid state dynamic-mechanical response and mechanical tensile properties. In particular, the effect on the blend properties of prolonging the irradiation time was investigated. Furthermore, a morphological characterization through atomic …

Materials sciencePolymers and PlasticsGeneral Chemical EngineeringOrganic Chemistrychemistry.chemical_compoundNatural rubberPolymerizationchemistryvisual_artvisual_art.visual_art_mediumParticle sizeIrradiationIn situ polymerizationMethyl methacrylateComposite materialAcrylonitrileGlass transitionAdvances in Polymer Technology
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