We report the first synthesis of the epoxy resin/polyurethane (EP/PU) hybrid networks via frontal
polymerization (FP). In a typical run, the appropriate amounts of reactants (poly(propylene oxide glycol),
epoxy resin diglycidyl ether of bisphenol A, 2,4-toluene diisocyanate, and 1,4-butanediol with stannous
caprylate (as the catalyst)) were mixed together at initial temperature in the presence of toluene (as the
solvent). FP was thermally ignited at one end of the tubular reactor, and the resultant hot fronts propagated
throughout the reaction vessel. Once initiated, no further energy was required for polymerization to occur.
The dependence of the front velocity and front temperature on the catalyst concentration was thoroughly
investigated. The samples were characterized with a Fourier transform infrared spectrometer, thermogravimetric analysis, and a scanning electron microscope. EP/PU hybrid networks synthesized by FP
have the same properties as those synthesized by batch polymerization, but the FP method requires
significantly less time and lower energy input.
The immobilization of bovine serum albumins (BSA) onto cationic spherical polyelectrolyte brushes (SPB) consisting of a solid polystyrene (PS) core and a densely grafted poly(2-aminoethyl methacrylate hydrochloride) (PAEMH) shell was studied by small-angle X-ray scattering (SAXS). The observed dynamics of adsorption of BSA onto SPB by time-resolved SAXS can be divided into two stages. In the first stage (tens of milliseconds), the added proteins as in-between bridge instantaneously caused the aggregation of SPB. Then BSA penetrated into the brush layer driven by electrostatic attractions, and reached equilibrium in the second stage (tens of seconds). The amount of BSA immobilized onto brush layer reached the maximum when pH was increased to about 6.1 and BSA concentration to 10 g/L. The cationic SPB were confirmed to provide stronger adsorption capacity for BSA compared to anionic ones.
Core-shell-corona silica/polymer hybrid nanoparticles with narrow size distribution were prepared in the template of spherical polyelectrolyte brushes (SPB) which consist of a solid polystyrene (PS) core densely grafted with linear poly(acrylic acid) (PAA) chains. The microstructure of obtained hybrid nanoparticles was studied by small-angle X-ray scattering (SAXS) and in combination with dynamic light scattering (DLS) and transmission electron microscopy (TEM). The generation of silica shell within the brush is confirmed by the significant increase of the electron density in the shell, and the silica shell showed a unique inner-loose-outer-dense structure, whose thickness is pH sensitive but is insensitive to ionic strength as revealed by fitting SAXS data. After dissolving the PS core, hollow silica nanoparticles were obtained and determined by SAXS, which should be ideal carriers for pH-triggered drug delivery. SAXS is confirmed to be a powerful method to characterize the core-shell-corona silica/polymer hybrid and hollow silica nanoparticles.
We report the first synthesis of urethane-acrylate copolymers via freeradical frontal polymerization. In a typical run, the appropriate amounts of the reactants (urethane-acrylate macromonomer and 2-hydroxyethyl acrylate) and initiator (ammonium persulfate) were dissolved in dimethyl sulfoxide. Frontal polymerization was initiated by the heating of the wall of the tube with a soldering iron, and the resultant hot fronts were allowed to self-propagate throughout the reaction vessel. Once it was initiated, no further energy was required for the polymerization to occur. The dependence of the front velocity and front temperature on the initiator concentration was investigated. The front temperatures were between 55 and 65 8C, depending on the persulfate concentration. Thermogravimetric analysis indicated that the urethaneacrylate copolymers had higher thermal stability than pure frontally prepared polyurethane. V V C 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: [3018][3019][3020][3021][3022][3023][3024] 2006
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.