Search results for "polymerization"
showing 10 items of 1689 documents
A practical ethylene polymerization for vinyl-polyethylenes: synthesis, characterization and catalytic behavior of α,α’-bisimino-2,3:5,6- bis(pentame…
2016
A series of α,α′-bis(arylimino)-2,3:5,6-bis(pentamethylene)pyridyliron chlorides was synthesized in a one-pot reaction and characterized by FT-IR and elemental analysis as well as X-ray crystallography for one representative iron complex, where the Fe center adopts a distorted square pyramidal geometry with three coordinating nitrogen and two chlorine atoms. The iron precatalysts, upon treatment with either methylaluminoxane (MAO) or modified methylaluminoxane (MMAO), exhibit high activities in the range of 107 g of PE per mol of Fe per h toward ethylene polymerization, yielding highly linear and, more importantly, vinyl-polyethylenes. The correlation between the structural features of iron…
Finely tuned nickel complexes as highly active catalysts affording branched polyethylene of high molecular weight: 1-(2,6-Dibenzhydryl-4- methoxyphen…
2018
Abstract A series of unsymmetrical 1,2-bis(imino)acenaphthenenickel(II) halides containing N-2,6-dibenzhydryl-4-methoxyphenyl – a single bulky group with adjusted electron donating properties – has been synthesized and characterized. These compounds adopt distorted tetrahedral geometry and their 1H NMR spectra show the paramagnetically shifted peaks. On activation with a low amount of Et2AlCl or ethylaluminum sesquichloride (EASC), these nickel complexes display high activity in ethylene polymerization, yielding the polyethylene of high molecular weight. They are also stable at elevated temperature; superb activity of 2.51 × 106 g of PE (mol of Ni)−1 h−1 can be attained at 90 °C. The result…
The apparently anomalous effects of surfactants on interfacial tension in the IBA/water system near its upper critical solution temperature
2016
We studied the effect of anionic, cationic, and nonionic surfactants on the interfacial tension between the two phases of the isobutyric acid/water system using spinning drop tensiometry. It has been found that interfacial tension decreases with increasing concentration of the surfactant in the case of sodium dodecyl sulfate (SDS) and of dodecyltrimethylammonium chloride (DTAC). However, in the case of Triton X-100 an increase of surfactant concentration leads to an increase of the interfacial tension. Such results are consistent with the upper critical solution temperature (UCST) in the presence of these surfactants: the UCST decreases with increasing SDS and DTAC concentrations while it i…
Multi-Alkenylsilsesquioxanes as Comonomers and Active Species Modifiers of Metallocene Catalyst in Copolymerization with Ethylene.
2018
The copolymers of ethylene (E) with open-caged iso-butyl-substituted tri-alkenyl-silsesquioxanes (POSS-6-3 and POSS-10-3) and phenyl-substituted tetra-alkenyl-silsesquioxane (POSS-10-4) were synthesized by copolymerization over the ansa-metallocene catalyst. The influence of the kind of silsesquioxane and of the copolymerization conditions on the reaction performance and on the properties of the copolymers was studied. In the case of copolymerization of E/POSS-6-3, the positive comonomer effect was observed, which was associated with the influence of POSS-6-3 on transformation of the bimetallic ion pair to the active catalytic species. Functionality of silsesquioxanes and polymerization par…
Biodegradable hyperbranched polyether-lipids with in-chain pH-sensitive linkages
2016
Hyperbranched polyether-based lipids with cleavable acetal units were obtained via copolymerization of the epoxide inimer 1-(glycidyloxy)ethyl ethylene glycol ether (GEGE) and glycidol, using anionic ring-opening polymerization. Cholesterol-linear polyglycerol (Ch-linPG) was used as a macroinitiator, resulting in branched polyethers with an adjustable amount of acid-cleavable units. Random copolymerization led to Ch-P(GEGEx-co-Gy) copolymers, whereas sequential copolymerization provided access to Ch-P(GEGEx-b-Gy) amphiphiles. The amount of GEGE was varied between 8–49 mol% of the total amount of monomer units. In addition, hyperbranched polyethers with a single acetal unit were prepared usi…
A New Hyaluronic Acid Derivative Obtained from Atom Transfer Radical Polymerization as a siRNA Vector for CD44 Receptor Tumor Targeting
2015
Two derivatives of hyaluronic acid (HA) have been synthesized by atom transfer radical polymerization (ATRP), starting from an ethylenediamino HA derivative (HA-EDA) and by using diethylaminoethyl methacrylate (DEAEMA) as a monomer for polymerization. Both samples, indicated as HA-EDA-pDEAEMA a and b, are able to condense siRNA, as determined by gel retardation assay and resulting complexes show a size and a zeta potential value dependent on polymerization number, as determined by dynamic light scattering measurements. In vitro studies performed on HCT 116 cell line, that over express CD44 receptor, demonstrate a receptor mediated uptake of complexes, regardless of their surface charge.
New copolymers graft of α,β-poly(N-2-hydroxyethyl)-d,l-aspartamide obtained from atom transfer radical polymerization as vector for gene delivery
2012
Abstract New cationic α,β-poly(N-2-hydroxyethyl)- d , l -aspartamide (PHEA) graft copolymers were synthesized by ATRP, using diethylamino ethyl methacrylate (DEAEMA) as monomer for polymerization, yielding polycations (PHEA-pDEAEMA) able to condense DNA. Then, consecutive ATRP conditions were set up on PHEA-pDEAEMA to obtain copolymers containing also hydrophilic chains (PHEA-IB-pDMAEMA-pPEGMA) able to improve biocompatibility of polyplexes and to provide them stealth properties. Agarose gel studies showed that the copolymers effectively condensed plasmid DNA to form polyplexes. Light scattering studies were used to analyze the size and the ζ -potential of these polyplexes, showing that cop…
Acid‐Labile Amphiphilic PEO‐ b ‐PPO‐ b ‐PEO Copolymers: Degradable Poloxamer Analogs
2016
Poly ((ethylene oxide)-b-(propylene oxide)-b-(ethylene oxide)) triblock copolymers commonly known as poloxamers or Pluronics constitute an important class of nonionic, biocompatible surfactants. Here, a method is reported to incorporate two acid-labile acetal moieties in the backbone of poloxamers to generate acid-cleavable nonionic surfactants. Poly(propylene oxide) is functionalized by means of an acetate-protected vinyl ether to introduce acetal units. Three cleavable PEO-PPO-PEO triblock copolymers (Mn,total = 6600, 8000, 9150 g·mol(-1) ; Mn,PEO = 2200, 3600, 4750 g·mol(-1) ) have been synthesized using anionic ring-opening polymerization. The amphiphilic copolymers exhibit narrow molec…
Kinetic Analysis of “Living” Polymerization Systems Exhibiting Slow Equilibria. 3. “Associative” Mechanism of Group Transfer Polymerization and Ion P…
1996
The averages of the molecular weight distribution are derived for a “living” polymerization process which proceeds via active and “dormant” species and where the active species are formed by addition of a catalyst to a “dormant” species. Such a mechanism is applicable to group transfer and “living” cationic polymerizations (assuming that ion pairs are formed exclusively in the latter case). Both equilibrium and nonequilibrium initial conditions are used for the calculation. The results are very similar to those obtained for degenerative transfer (i.e., direct exchange of activity between active and “dormant” species). The dominating parameter is β = k2/(kpI0), where k2 and kp are the rate c…
Diffusion of single molecular and macromolecular probes during the free radical bulk polymerization of MMA : towards a better understanding of the Tr…
2016
Free radical bulk polymerizations exhibit complex kinetics due to the viscosity increase during the polymerization process. Especially the termination rate constant can be strongly influenced by the mobility of polymer chains in the polymerization mixture. As a consequence an autoacceleration period, the so-called Trommsdorff effect, can be observed often. In order to investigate this behaviour on a nanoscopic scale, we directly visualized the mobility of molecules and macromolecules in polymerizing MMA solutions using a combination of highly sensitive fluorescence correlation spectroscopy and widefield fluorescence microscopy. For this purpose, rather monodisperse PMMA chains were synthesi…