The synthesis of nanosized poly(methyl methacrylate) initiated by 2,2′‐azoisobutyronitrile via differential microemulsion polymerization has been investigated. Poly(methyl methacrylate) with a molecular weight of around 1 × 106 and a particle size of about 20 nm was achieved under mild reaction conditions. A typical condition was that the surfactant amount required could be as low as 1/130 of the monomer amount in weight, and the surfactant/water ratio could be as low as 1/600, which is much less than the corresponding amounts reported in the literature. “Molecular bricks”, i.e., nanoparticles in which there are only one or two polymer chains, can be achieved using mild conditions by differential microemulsion polymerization, which may have potential applications for making molecular devices.
Reversible addition–fragmentation chain transfer (RAFT) chemistry can be effectively employed to construct macromolecular architectures of varying topologies. The present article explores the principle design routes to star, block, and comb polymers in the context of theoretical design criteria for the so‐called Z‐ and R‐group approaches. The specific advantages and disadvantages of each approach are underpinned by selected examples generated in the CAMD laboratories. In particular, we demonstrate how the modeling of full molecular weight distributions can be employed to guide the synthetic effort. We further explore the theory and practice of generating amphiphilic block copolymer structures and their self‐assembly. In addition, the article foreshadows how modern synthetic techniques that combine RAFT chemistry with highly orthogonal click chemistry can be employed as a powerful tool that furthers the enhancement of macromolecular design possibilities to generate block (star) copolymers of monomers with extremely disparate reactivities. Finally, the ability of RAFT chemistry to modify the surface of well‐defined nano‐ and microspheres as devices in biomedical application is detailed.
Summary: Process intensification is investigated by the emulsion polymerization of styrene in the continuous Taylor reactor. The result is an increase in space time yield up to a factor 200 in comparison to a semi-batch polymerization process. This is obtained by a fast emulsion polymerization with a mean residence time, which is reduced to 60 seconds. The article presented the results of the process and the economical aspects of the Taylor reactor plant. 相似文献
Summary: Graft copolymerization of N-isopropyl acrylamide and methyl acrylate on α-cellulose was carried out under microwave irradiation at specific cut off temperatures with cerium (IV) ammonium nitrate and potassium persulfate (KPS) as the initiating system. The role of KPS was to oxidize Ce (III) to Ce (IV) which is the active species in radical formation. The reactions at a temperature cut off of 60 °C were confirmed by 13C nuclear magnetic resonance cross-polarization with magic- angle spinning (13C NMR CP/MAS) and Fourier-transform infrared spectroscopy (FTIR). The extent of grafting was calculated from weight gain and 13C resonances. The grafted cellulose was thermally more stable than the parent cellulose. An attempt to do grafting at a higher cut off temperature of 80 °C was made, however, no grafting was observed from 13C NMR CP/MAS but TGA results showed that a cellulose having more thermal stability resulted which was attributed to cross linking. Crystallization of CaCO3 was carried out using the grafted materials as templates showed better nucleation and different crystal structure was observed. 相似文献
The results of experiments in which bore-type waves with various leading front shapes propagated first above an even horizontal bottom, then above a rising bottom, then again above a horizontal bottom segment, and were finally reflected from a vertical wall are presented. It is shown that the impact force is greatest if the leading front breaks directly on approaching the wall. This force is much greater than the impact force of smooth waves or waves that break before they reach the wall. 相似文献