Search results for "opolymerization"

showing 10 items of 56 documents

(Co)polymerization behavior of supported metallocene catalysts. I. Ligand and substituent effect

2005

Ethylene polymerization and its copolymerization with 1-hexene with a set of supported metallocene catalysts were studied. As a carrier, the complex of mag- nesium chloride with tetrahydrofuran, which was previously pretreated with a triiso- butylaluminium (TIBA), was used. The investigated metallocene compound differs in the metal type (Zr or Ti), the nature of the alkyl substituent in the cyclopentadienyl ring, and the type of ligand (Cp or Ind). The effect of catalyst composition on the anchored metal content, catalyst activity, comonomer reactivity, and polymer proper- ties was investigated. The results obtained with supported catalysts were compared with those obtained with their homog…

chemistry.chemical_classificationsupportPolymers and PlasticsComonomermetallocene catalystsOrganic ChemistrySubstituentHomogeneous catalysiscopolymerizationchemistry.chemical_compoundchemistryCyclopentadienyl complexPolymerizationPolymer chemistryMaterials ChemistrystructureMetalloceneTetrahydrofuranAlkylJournal of Polymer Science Part A: Polymer Chemistry
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(Co)polymerisation Behaviour of Supported Metallocene Catalysts: Carrier Effect

2006

The polymerisation and copolymerisation of ethylene with 1-hexene over metallocene catalysts L 2 ZrCl 2 / MAO (L = Cp, n-BuCp, t-BuCp, i-PrCp, Me 5 Cp) supported on different types of carriers (MgCl 2 (MeOH) 6 or silica with CH 3 surface groups obtained in the sol-gel process) were studied. It was demonstrated that both the metallocene structure and the type of inorganic support affected catalyst activity and polymer properties such as melting point, molecular weight and molecular weight distribution. The metallocene structure also determined comonomer incorporation, both for homogeneous and supported catalytic systems. When a catalyst is anchored on a support, it becomes less effective at …

chemistry.chemical_classificationsupportsPolymers and PlasticsComonomermetallocene catalystsOrganic ChemistryPolymerPolyethyleneCondensed Matter PhysicsCatalysischemistry.chemical_compoundchemistryPolymerizationPolymer chemistryopolymerizationMaterials ChemistryCopolymerMolar mass distributionstructurePhysical and Theoretical ChemistryCrystafSSAMetalloceneMacromolecular Chemistry and Physics
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Methacrylic maleic bifunctional stabilizer in emulsion polymerization

1998

chemistry.chemical_compoundMaterials sciencePolymers and PlasticschemistryOrganic ChemistryPolymer chemistryRadical polymerizationMaterials ChemistryEmulsion polymerizationBifunctionalEmulsion copolymerizationStabilizer (chemistry)Macromolecular Rapid Communications
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Electrocatalytic properties of manganese and cobalt polyporphine films toward oxygen reduction reaction

2018

International audience; Novel member of polymetalloporphines, namely manganese polymetalloporphine of type I (pMnP-I) obtained by ion exchange from magnesium polyporphine of type I (pMgP-I) is reported for the first time and compared to its cobalt analogue (pCoP-I). Both polymer films have been obtained via two-step procedure: demetaladon of the pMgP-I electrode film via its exposure to trifluoroacetic acid solution, resulting in formation of the metal-free polyporphine of type I (pH(2)P-I) followed by electrochemically induced incorporation of Co or Mn ions from the acetonitrile solution of cobalt and manganese perchlorates. A further oxidative transformation of pCoP-I, polymer films has l…

conjugated porphyrin polymerGeneral Chemical EngineeringInorganic chemistryFOS: Physical scienceschemistry.chemical_element02 engineering and technologyElectrolyteManganesepositive potentialsphthalocyanines010402 general chemistry01 natural sciencescatalystsAnalytical ChemistryCatalysisporphine[CHIM.ANAL]Chemical Sciences/Analytical chemistryframeworksElectrochemistry[CHIM]Chemical Sciencesdioxygen reductionCondensed Matter - Materials SciencemetalloporphyrinsAqueous solutionIon exchangeMagnesiumElectroactive polymersMaterials Science (cond-mat.mtrl-sci)Oxygen electroreductionelectropolymerizationfuel-cell cathode021001 nanoscience & nanotechnologyMetalloporphines0104 chemical sciencesPolymer film coated electrodechemistry0210 nano-technologyPlatinumCobaltMg(II) porphineJournal of Electroanalytical Chemistry
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Modeling Heterogeneous copolymerization of fluorinated monomers in scCO2

2009

In recent years the use of supercritical carbon dioxide (scCO2) in polymer processing and reaction has emerged as a “green” alternative to replace both environmentally hazardous organic solvents and water, whose utilization involves the production of large amount of waste streams. Moreover, scCO2 is non-toxic, inexpensive, and often exhibits intense plasticizing effect on polymers. In this work, the copolymerization of fluorinated monomers in scCO2 is explored. Batch free-radical copolymerization reactions of vinylidene fluoride (VDF) and hexafluoropropylene (HFP) have been carried out at temperature of 50 C and pressure of 400 bar using DEPDC as initiator and different amounts of stabilize…

copolymerization carbon dioxide modeling heterogeneous reaction
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Application of Silsesquioxanes in the Preparation of Polyolefin-Based Materials

2023

This paper is a review of studies on the use of the polyhedral oligomeric silsesquioxanes (POSS) of various structures in the synthesis of polyolefins and the modification of their properties, namely: (1) components of organometallic catalytic systems for the polymerization of olefins, (2) comonomers in the copolymerization with ethylene, and (3) fillers in composites based on polyolefins. In addition, studies on the use of new silicon compounds, i.e., siloxane–silsesquioxane resins, as fillers for composites based on polyolefins are presented. The authors dedicate this paper to Professor Bogdan Marciniec on the occasion of his jubilee.

copolymerizationPOSS-comonomersiloxane–silsesquioxane resinpolymerizationtransition metal–silsesquioxane complexcompositepolyolefinsolefinPOSScatalystMaterials
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Wpływ wybranych parametrów na efektywność katalizowanej wanadocenem kopolimeryzacji etylenu z norbornenem i właściwości otrzymanych produktów

2019

W pracy zbadano wpływ parametrów reakcji na kopolimeryzację etylenu z norbornenem wobec katalizatora wanadocenowego (Cp2VCl2) w obecności trichloroctanu etylu (ETA). Przeprowadzono serię reakcji kopolimeryzacji, zmieniając w każdej z nich jeden z parametrów reakcji: temperaturę lub ciśnienie etylenu. Następnie zbadano temperaturę zeszklenia, stopień wbudowania norbornenu i mikrostrukturę otrzymanych kopolimerów, poddając je analizie DSC oraz spektroskopii 13C NMR. Wykazano wpływ badanych parametrów na aktywność katalizatora oraz ilość i sposób wbudowania jednostek norbornenu w łańcuch polimerowy, jak również wartość temperatury zeszklenia produktu. Stwierdzono, że właściwości otrzymanego ko…

copolymerizationkopolimer etylen/norbornenreaction parameterskatalizator wanadowyethylene/norbornene copolymervanadium catalystkopolimeryzacjanorbornenenorbornenparametry reakcji
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Copolymerization of Vinylidene Fluoride and Acrylic Acid in Supercritical Carbon Dioxide

2010

The free-radical copolymerization of vinylidene fluoride (VDF) and acrylic acid (AA) was carried out in supercritical carbon dioxide using both precipitation and dispersion techniques in the presence of an ammonium carboxylate perfluoropolyether compound. Formation of a copolymer was confirmed by variable contact time CP MAS NMR spectroscopy. Macromolecular matrices were significantly enriched in AA with respect to the initial feed composition and we found that the nonfluorinated monomer has a much higher reactivity ratio with respect to VDF. The cumulative concentration, crystallinity, and water affinity of the synthesized copolymers could be modified changing the initial feed composition,…

copolymerizationsupercritical fluidacrylic acidfluoropolymervinylidene fluorideSettore ING-IND/27 - Chimica Industriale E Tecnologicamembraneradical polymerizationfreeradical copolymerization
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Copolymerization of Ethylene with Selected Vinyl Monomers Catalyzed by Group 4 Metal and Vanadium Complexes with Multidentate Ligands: A Short Review

2021

This paper gives a short overview of homogeneous post-metallocene catalysts based on group 4 metal and vanadium complexes bearing multidentate ligands. It summarizes the catalytic behavior of those catalysts in copolymerization of ethylene with 1-olefins, with styrenic monomers and with α,ω-alkenols. The review is focused on finding correlations between the structure of a complex, its catalyst activity and comonomer incorporation ability, as well as the microstructure of the copolymer chains.

copolymerizationω-alkenolQD241-441Polymers and Plasticsαpost-metallocene catalyst1-olefinethyleneOrganic chemistryReviewGeneral Chemistryαω-alkenolstyrenic monomerPolymers
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Synthesis and characterization of ethylene-1-hexene copolymers prepared by using MgCl2(THF)2-supported Ziegler-Natta catalysts

2000

Ethylene was copolymerized with 1-hexene over vanadium (VOCl3 and VCl4) and titanium (TiCl4) catalysts supported on MgCl2(THF)2 and activated with Et2AlCl. So far these catalyst systems have not been known as initiators of ethylene-1-hexene copolymerization. The vanadium catalysts were more active than the titanium catalyst and, at identical comonomer concentrations in the feed, gave rise to a greater incorporation of 1-hexene into the copolymer. Even at relatively low fractions of 1-hexene, the MgCl2(THF)2-supported catalysts affected much the copolymer properties like density, melting point and crystallinity.

densityMaterials scienceEthylenePolymers and PlasticsbiologyGeneral Chemical Engineeringcopolymerization of ethylene with 1-hexeneVOCl3melting point and crystallinity of copolymarsNattabiology.organism_classificationCharacterization (materials science)Catalysis1-Hexenechemistry.chemical_compoundchemistryVCl4 and TiCl4 catalysts supported on MgCl2(THF0)2 and activated with Et2AlClPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryPolimery
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