Search results for "Anionic addition polymerization"

showing 10 items of 110 documents

1991

Telechelic α,ω-macrozwitterions — narrowly distributed polystyrene chains oppositely charged at each end — were synthesized via anionic polymerization using direct functionalization with the initiator and the termination agent. The resulting products were purified (zwitterion content ≥ 0,95) and characterized with gel permeation chromatography, viscometry, static and dynamic light scattering and small-angle neutron scattering. In unpolar solvents as toluene, the polymeric zwitterions form clusters with molecular weights depending on concentration. In the dilute case, the clusters are relatively small and consist of approximately 8 zwitterions. The structure of these clusters is discussed by…

chemistry.chemical_classificationchemistry.chemical_compoundEnd-groupTelechelic polymerAnionic addition polymerizationchemistryDynamic light scatteringZwitterionPolymer chemistryPolymerPolystyreneSmall-angle neutron scatteringDie Makromolekulare Chemie
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Electrochemical production of initiators for polymerization processes

2007

The most important technological interest in initiator production lies, in the electrosynthesis of complex catalytic systems, i. e. coordination compounds and Ziegler-Natta catalysts, although the choice of olefins to be polymerized with these electrosynthesized complexes is still limited to ethylene and to very few other monomers.

chemistry.chemical_classificationchemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationCationic polymerizationReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationElectrosynthesisCombinatorial chemistryCoordination complex
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Synthesis and thermoresponsive properties of four arm, amphiphilic poly(tert-butyl-glycidylether)-block-polyglycidol stars

2011

Abstract A series of four arm stars with copolymer arms composed of poly(tert-butyl-glycidylether)-b-polyglycidol were prepared using a multi-step process based on anionic ring-opening polymerization. Control of the length of the arms and the number of functional (hydroxyl) reactive groups was achieved by anionic polymerization. Stars with molar masses up to 12200 g/mol were prepared. The amphiphilic character of the star structure was varied using different polyglycidol block lengths. The star structure and molar mass of the obtained stars were characterized by SEC–MALLS and NMR spectroscopy. The temperature behavior of an aqueous solution of the obtained polymers was also investigated. Th…

chemistry.chemical_classificationendocrine systemMaterials scienceMolar massAqueous solutionPolymers and PlasticsOrganic ChemistryNuclear magnetic resonance spectroscopyPolymerAnionic addition polymerizationchemistryPolymerizationAmphiphilePolymer chemistryMaterials ChemistryCopolymerPolymer
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1980

chemistry.chemical_compoundAnionic addition polymerizationChemistryKineticsPolymer chemistryMethyl methacrylateIonic polymerizationPhotochemistryDimethoxyethaneLiving anionic polymerizationDie Makromolekulare Chemie, Rapid Communications
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1974

chemistry.chemical_compoundAnionic addition polymerizationMonomerReaction rate constantChemistryPolymer chemistryMethyl methacrylateDie Makromolekulare Chemie
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1978

A newly designed automatically controlled stirred reactor suitable for kinetic measurements of reactions with half lives ≥2s has been applied to follow the anionic polymerization of methyl methacrylate in THF with Na+ as a counter ion in the presence of an excess of NaB(C6H5)4. As initiators were used: benzylsodium reacted with α-methylstyrene (I), fluorenylsodium (II), and 9-methylfluorenylsodium (III). With I the initiation is fast as compared with the polymerization reaction which is first order in monomer concentration. Within the range of −50°C to −100°C an almost unperturbed “living” polymerization is observed. The Arrhenius plot of the rate constants results in a straight line with a…

chemistry.chemical_compoundAnionic addition polymerizationMonomerReaction rate constantPolymerizationChemistryTacticityPolymer chemistryActivation energyMethyl methacrylateArrhenius plotDie Makromolekulare Chemie
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1984

The decomposition reactions of the lithiated dimer, trimer, and tetramer of methyl methacrylate (MMA) in THF at 25°C were investigated. The decomposition of the lithiated dimer proceeds via depolymerization to lithiated monomer and MMA, addition of MMA to residual lithiated dimer, resulting the trimer (“disproportionation” of the dimer), and subsequent autocondensation of the products. The lithiated trimer almost exclusively undergoes cyclo-autocondensation, whereas for the lithiated tetramer both reactions proceed simultaneously to a remarkable degree. It is shown that the relative rate of autocondensation, which is highly dependent on the degree of polymerization of the oligomer, controls…

chemistry.chemical_compoundAnionic addition polymerizationMonomerTetramerChemistryDepolymerizationDimerPolymer chemistryfood and beveragesDisproportionationTrimerDegree of polymerizationDie Makromolekulare Chemie
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Theoretische analyse der bei einem zweiwegwachstumsmechanismus auftretenden molekulargewichtsverteilungen und ihre anwendung auf die anionische polym…

1967

Es werden mittels der Momentmethode die fur einen abbruchfreien Zweiwegwachstumsmechanismus zu erwartenden Molekulargewichtsverteilungen und ihr Zusammenhang mit dem kinetischen Ablauf theoretisch abgeleitet. Die ermittelten Bezichungen werden auf das Polymerisationssystem Styrol in Cumylmethylather mit Cumylnatrium als Initiator angewandt. Durch Einsetzen der vorher experimentell ermittelten kinetischen Daten in die theoretisch abgeleitete Gleichung werden die Molekulargewichtsverteilungen des untersuchten Systems berechnet und mit den experimentell ermittelten verglichen. Die gute Ubereinstimmung zwischen Theorie und Experiment stellt einen schlussigen Beweis fur das Vorliegen eines Zweiw…

chemistry.chemical_compoundAnionic addition polymerizationPolymerizationChemistryPolymer chemistryEtherStyreneDie Makromolekulare Chemie
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Kinetics of Group Transfer Polymerization

1987

The group transfer polymerization (GTP) of methyl methacrylate (MMA) and tert.-butyl methacrylate (TBMA), catalyzed by bifluoride, is of first order with respect to monomer and catalyst concentrations. A slightly negative order with respect to initiator concentration is observed, indicating an inhibitive function of the initiator. Termination reactions occur at lower catalyst concentrations. They are very pronounced for TBMA and result in incomplete conversions. For MMA, at lower catalyst and higher initiator concentrations, induction periods are observed which increase when lowering the temperature. This is related with the formation of active chains. The Arrhenius plots for the propagatio…

chemistry.chemical_compoundAnionic addition polymerizationPolymerizationchemistryInduction periodPolymer chemistryRadical polymerizationLiving polymerizationChain transferMethyl methacrylateIonic polymerization
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Herstellung, charakterisierung und lösungseigenschaften von einheitlichen styrol-α-methylstyrol block-copolymeren

1977

An improved anionic polymerization technique for the preparation of highly uniform styrene/α-methylstyrene linear two-block copolymers is described. Three sets of samples with molecular weights M were prepared under equal experimental conditions, namely polystyrenes (2 · 105 < M < 3 · 106), poly(α-methylstyrene)s (7 · 104 < M < 4 · 106), and block copolymers (2 · 105 < M < 2,5 · 106). Ultracentrifugation in a density-gradient does not show any chemical heterogeneities in the block copolymers. The molecular polydispersity U = Mw/Mn–1 is U = 0,03 or less as estimated from GPC-measurements. The high molecular and chemical homogeneity of the block copolymers and the optical similarity of the tw…

chemistry.chemical_compoundAnionic addition polymerizationVirial coefficientchemistryIntramolecular forceDispersityPolymer chemistryCopolymerGyrationTolueneStyreneDie Makromolekulare Chemie
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