Search results for "polymerization"
showing 10 items of 1689 documents
PREPARATION OF OLIGOMERS WITH FUNCTIONAL END GROUPS BY POLYMERIZATION REACTIONS
1973
ABSTRACT The possibilities of preparing oligomers with functional end groups by cationic, anionic and radical polymerization are discussed. Special attention is given to oligomers with two functional end groups (telechelic oligomers). By use of efficient separation techniques, especially GPC, these oligomers can be separated and analyzed. The conclusions that can be drawn from the structure of these oligomers with respect to the elementary processes in polymerization reactions are critically examined.
Optimization of spinning, drawing, and annealing conditions in the production of highly oriented fibers from the polycaprolactam/3.7% LiCl system
1982
A polycaprolactam/3.7% w/w LiCl system, obtained by anionic polymerization of caprolactam directly in the presence of salt, has been employed for the production of highly oriented fibers. More particularly, an optimization of spinning, drawing, and annealing conditions has been performed, finally obtaining fibers which shows very satisfactory mechanical results. Namely, average moduli values up to 12 GPa and strength values up to 1 GPa when fracture is far from clamps, have been observed.
Highly Ordered Nanoporous Thin Films from Photocleavable Block Copolymers
2011
Poly(styrene-block-ethylene oxide) with an o-nitrobenzyl ester photocleavable junction (PS-hν-PEO) was synthesized by a combined RAFT polymerization and “click chemistry“ approach and represents the first report utilizing this method for the synthesis of photocleavable block copolymers. After solvent annealing, highly ordered thin films were prepared from PS-hν-PEO. Following a very mild UV exposure and successive washing with water, PS-hν-PEO thin films were transformed into highly ordered nanoporous thin PS films with pore diameters of 15–20 nm and long range ordering (over 2 μm × 2 μm). Afterwards the pores were filled with PDMS by spin-coating in combination with capillary forces. After…
Poly(N-isopropylacrylamide) and Copolymers: A Review on Recent Progresses in Biomedical Applications.
2017
The innate ability of poly(N-isopropylacrylamide) (PNIPAAm) thermo-responsive hydrogel to copolymerize and to graft synthetic polymers and biomolecules, in conjunction with the highly controlled methods of radical polymerization which are now available, have expedited the widespread number of papers published in the last decade—especially in the biomedical field. Therefore, PNIPAAm-based hydrogels are extensively investigated for applications on the controlled delivery of active molecules, in self-healing materials, tissue engineering, regenerative medicine, or in the smart encapsulation of cells. The most promising polymers for biodegradability enhancement of PNIPAAm hydrogels are probably…
Surfactant-Free Emulsion Polymerization of Various Methacrylates: Towards Monodisperse Colloids for Polymer Opals
2004
A systematic investigation of the surfactant-free emulsion polymerization (SFEP) on three different methacrylates (MMA, tert-butyl methacrylate and 2,2,2-trifluoro ethyl methacrylate) is described to obtain monodisperse colloids for the preparation of artificial polymer opals. The experimental results are in agreement with a model, in which seed particles are formed very early during the polymerization process. The particles are formed very early during the polymerization process. The particles grow afterwards into the colloids until all monomer is consumed. This gives rise to a linear relationship between the volume of the colloids and the ratio of monomer to water in the reaction batch. T…
Carbanions on Tap – Living Anionic Polymerization in a Microstructured Reactor
2008
The paper describes the living anionic polymerization of styrenes to homo- and diblock copolymers in continuous flow, using a microstructured mixing set-up ("microreactor"). Reaction times and experimental effort are significantly reduced compared to classical batch methods that often require stringent reaction conditions and strict drying of the apparatus by "break-seal" and "high vacuum" techniques. In continuous flow, residual impurities can be removed by purging the reactor with monomer and initiator solution before polymer samples are collected at the device outlet on a scale of up to 200 g.h -1 . Facile molecular weight adjustment is achieved by variation of the flow rates of initiato…
Macromonomers on the basis of 2-phenyl-2-oxazoline
1988
By initiation of the ring-opening polymerization of 2-phenyl-2-oxazoline (1) with p-iodomethylstyrene a macromonomer with a styrene end-group (2) is obtained. The degree of polymerization was varied between 10 and 16. The radical copolymerization of 2 with styrene is described. 1 forms with methyl triflate a very stable oxazolinium salt which is a good initiator for the bulk polymerization of 1 at temperatures of 50–70°C. It was conclusively proved that under these conditions the polymerization proceeds by a living mechanism. By termination with N, N-dimethylaminopropylmeth-acrylamide a macromonomer (5) was obtained. 5 can be radically homopolymerized. This comb-like polymer 6 has the typic…
Synthesis of block copolymers with poly(methyl methacrylate): P(B-b-MMA), P(EB-b-MMA), P(S-b-B-b-MMA) and P(S-b-EB-b-MMA)
1993
Well-defined diblock copolymers poly(butadiene-b-methyl methacrylate) (=P(B-b-MMA)) and triblock copolymers poly(styrene-b-butadiene-b-methyl methacrylate) (=P(S-b-B-b-MMA)) have been prepared by sequential anionic polymerization in THF. The synthesis of P(B-b-MMA) and P(S-b-B-b-MMA) was most efficient in the presence of lithium alkoxides. By this method side reactions are suppressed and the polymerization can be performed at higher temperatures. The resulting triblock copolymers have narrow molecular weight distribution. The 1,2-PB midblock was quantitatively hydrogenated with tosylhydrazide to enhance thermal stability. Alternatively the hydrogenation can be performed at elevated pressure…
Reductive Decationizable Block Copolymers for Stimuli-Responsive mRNA Delivery
2016
Messenger ribonucleic acids (mRNAs) are considered as promising alternatives for transient gene therapy, but to overcome their poor pharmacokinetic properties, smart carriers are required for cellular uptake and stimuli-responsive release. In this work, a synthetic concept toward reductive decationizable cationic block copolymers for mRNA complexation is introduced. By combination of RAFT block copolymerization with postpolymerization modification, cationic block copolymers are generated with disulfide-linked primary amines. They allow effective polyplex formation with negatively charged mRNA and subsequent release under reductive conditions of the cytoplasm. In first in vitro experiments w…
A contribution to the kinetics of the polymerization of styrene with CF3SO3H as catalyst
1978
The time dependence of the cationic polymerization of styrene in CH2Cl2 with CF3SO3H as catalyst can be formally described as being first-order with respect to monomer concentration [M]0. The reaction rate shows a third-order dependence in catalyst concentration [C]0. A high polymer and a low polymer polystyrene fraction are found at [M]0>0.2 mole · l−. The reaction rate of the high polymer fraction is proportional to [C] 0 3 , that of the low polymer fraction probably proportional to [C] 0 2 . The polymerization active species may thus be triple ions in the first and ion pairs in the second case.