RAFT inverse miniemulsion polymerization is demonstrated for the first time as an alternate way to synthesize hydrophilic polymer latexes. The kinetic behavior of inverse RAFT miniemulsion polymerization of acrylamide is similar to that observed in aqueous RAFT solution polymerization. A water‐soluble initiator provides better control than a lipophilic initiator in inverse RAFT miniemulsion polymerization under the conditions used here.
Enzymatic degradation of polylactic acid is studied experimentally and analytically. Gel permeation chromatography profiles obtained before and after the enzymatic degradation of polylactic acid (PLA) were introduced into the analysis based on a mathematical model. Previously developed techniques were successfully adapted to the analysis of an initial value problem consisting of an endogenous depolymerization model and an initial condition, and an inverse problem to determine the degradation rate for which the solution of the initial value problem also satisfies a final condition. Those problems were solved numerically and numerical results are introduced. Degradabilities of PLA and polyvinyl alcohol are compared.
The formation of oxazolidines from propionaldehyde and aliphatic β-aminoalcohols is complicated by the appearance of appreciable amounts of unsaturated Schiff bases. The simple Schiff base, often the dominant species when aromatic aldehydes react with amines, could not be detected in the present aliphatic systems. We conclude that in aliphatic systems the order of stability is and . The gem-dimethyl group α to nitrogen stablizes the heterocyclic ring remarkably. 相似文献
A novel semi‐interpenetrating polymer network based on alginate and poly(N‐isopropylacrylamide) (PNiPAAm) has been synthesized that shows response to temperature and magnetic fields. Highly homogeneous porous hydrogels are obtained by copolymerizing N‐isopropylacrylamide and bis‐acrylamide in the presence of an aqueous alginate solution. The synthesis of magnetic iron oxides by in‐situ oxidation of iron cations coordinated to the alginate network results in a hydrogel with an enhanced deswelling rate with respect to pure PNiPAAm.
Summary: Poly(dimethylsiloxane) (PDMS) star polymers having a nanosized silica particle as a core were prepared by reacting silica nanoparticles with monoglycidylether‐terminated poly(dimethylsiloxane). This star polymer was a hybrid material having an extremely high content of silica. The PDMS arms formed an organic domain to separate the silica particles and to prevent particle aggregation. The star polymers exhibited good thermal stability and high activation energy of their degradation reaction, in comparison to the linear PDMS polymer and the PDMS/silica blending materials. This star polymer can be used as a flame retardant for polymeric materials and this preparation technique can be applied to prepare other star polymers.
An SEM image of poly(dimethylsiloxane) star polymers having nanosized silica particles as a core. 相似文献
Multiwalled carbon nanotubes (MWNTs) have been introduced into blends of polycarbonate (PC) and poly(styrene‐acrylonitrile) (SAN) by melt mixing in a microcompounder. Co‐continuous blends are prepared by either pre‐compounding low amounts of nanotubes into PC or SAN or by mixing all three components together. Interestingly, in all blends, regardless of the way of introducing the nanotubes, the MWNTs were exclusively located within the PC phase, which resulted in much lower electrical resistivities as compared to PC or SAN composites with the same MWNT content. The migration of MWNTs from the SAN phase into the PC phase during common mixing is explained by interfacial effects.
Summary: The impact of a droplet on a solid surface, pre‐patterned with a barrier, was studied using a diffuse interface model. The effect of the wettability of the barrier material and the width of the barrier on droplet spreading was investigated. The results show that depending on the barrier wettability and width, the flow of the spreading droplet can be controlled and that the droplet may or may not overflow the barrier.
Droplet shapes with the corresponding velocity field for different barrier contact angles at ± = 1.5. 相似文献
A series of monodisperse six‐arm benzene‐cored star oligofluorenes are prepared by a divergent/convergent strategy, starting from the repetitive divergent synthesis of symmetrical ethynyl‐bridged oligofluorenes to the convergent Co‐catalyzed alkyne cyclotrimerization. The structures of these six‐arm molecules are fully characterized. The diameter of the largest molecule SF3 reaches ca. 3 nm. These highly substituted star‐shaped oligomers exhibit extremely high fluorescent quantum yields in solution and unexpected red‐shifted and broadened emission with fine structure in the film as a result of the formation of stable aggregates.
The B‐ala/AIBN PBZ system has a high extent of ring‐opening of oxazine because phenol‐containing oligomers are formed at the early stage of the curing process. As a result, the B‐ala/AIBN PBZ system possesses a relatively stronger intramolecular hydrogen bonding and lower surface energy than the pure B‐ala system at low temperature curing. In this context, poly(4‐vinyl pyridine), poly(4‐vinyl phenol) thin films and polycarbonate substrates, which lack liquid resistance, possess low surface free energy after modification with B‐ala/AIBN = 5/1 PBZ.
Small, organic, toxic compounds are not well eliminated by water‐treatment systems and eventually become concentrated in the human body. In this study, liposomes are employed to house aptamers with their own binding buffer. When small, organic, toxic compounds in water pass through a liposome barrier, only the target molecules are captured by the DNA aptamers inside the liposomes. The capture efficiency is not high when DNA aptamers are used in tap water. When DNA aptamers in liposomes are used, the capture efficiency increases more than 80%. The simultaneous and selective elimination of target toxicants is successfully performed for tap‐water samples containing toxicant mixtures.
In this study, the hydrophobic liquid template method was firstly used to prepare temperature sensitive, porous poly(N‐isopropylacrylamide) (PNIPAAm) hydrogel. During the radical polymerization, hydrophobic polydimethylsiloxane (PDMS) and surfactant sodium dodecyl sulfate (SDS) were used as liquid templates and stabilizer, respectively. After removal of the liquid templates, porous PNIPAAm hydrogel was obtained. This gel exhibited superfast shrinking properties when being transferred from below to above the lower critical solution temperature (LCST), which was ascribed to the interconnected porous structures.
Via a batch process in an autoclave, the foam processing of neat polylactide (PLA) and two different types of PLA/layered silicate nanocomposites has been conducted using supercritical carbon dioxide as a foaming agent. The morphological correlation between the dispersed silicate particles with nanometer dimensions in the bulk and the obtained closed‐cell structure of the foam is discussed. This is the first report that deals with the possibility of preparing biodegradable nanocellular polymeric foams via nanocomposite technology.
SEM image of the freeze‐fracture surface of a PLA/layered silicate foam, exhibiting closed‐cell structure. 相似文献
Magnetic nanomaterials have been studied in order to generate novel nanocomposites that display both the magnetic properties of the nanoparticles and the ability to self‐assemble of the amorphous block copolymer matrix. Towards this goal, iron oxide magnetic nanoparticles have been modified with PS brushes by ATRP in order to improve both the dispersion and the affinity of the nanoparticles with one of the blocks of a polystyrene‐block‐polybutadiene‐block‐polystyrene block copolymer. This method of preparation of nanocomposites opens new strategies for the generation of magnetic nanomaterials. The samples are characterized using DSC and atomic and magnetic force microscopies.
This paper describes a poly(dimethylsiloxane) (PDMS)‐based microfluidic platform for constructing the phase diagram of poly(N‐isopropyl acrylamide) (PNIPAM) in aqueous solution. The PNIPAM solution was delivered into a nanoliter chamber through the main microchannel. An osmotic pressure difference was established between the chamber and the control microchannel by flowing a high‐concentration salt solution in the control microchannel. Controlled evaporation of water resulted in increasing concentration of PNIPAM. A phase diagram of PNIPAM was built by measuring the cloud points at different concentrations, with a minimum point at ≈40 wt.‐%. The microfluidic platform has the advantages of low sample consumption and rapid heat exchange rates, and allows studying viscous polymer solution.
Micrometer‐sized polydiacetylene (PDA) vesicle patterns on titanium substrates have been successfully fabricated by using a micromolding in capillaries (MIMIC) technique. The shape and width of the PDA patterns are well matched with polydimethylsiloxane (PDMS) molds used in the MIMIC process. However, the thicknesses of the patterned films are less than the depths of the PDMS molds, which may be a consequence of the poor water wettability of the PDMS and/or low concentrations of the PDA solutions. Heat‐treatment of the solid substrate, immobilized with blue‐phase PDAs, induces a blue‐to‐red‐phase transition and results in the formation of patterned fluorescence images.
In light of the increasing demand for ultra rapid and mild conjugation chemistries for use in macromolecular chemistry, the present Feature Article provides a critical overview of the very latest developments in this field. The principal aim, therefore, is the provision of a quick selection guide to aid in the formulation of a design strategy for novel functional materials and to provide recommendations for future developments in the chemistries discussed.
