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Cross-linked polymer microspheres are widely used in biomedicine, flat panel display, analytical testing, in vitro diagnostics, semiconductor chips, and light diffusion. However, the process of preparing micron-sized cross-linked polymer microspheres is complicated, and it is difficult to obtain a high crosslinking degree conveniently. In this work, we applied post-crosslinking strategy to prepare poly (methyl methacrylate) (PMMA) microspheres having a high crosslinking degree by dispersion polymerization, while the method separated the polymerization process and cross-linking process of microspheres. In the method, the silane coupling agents containing double bonds were used as the comonomer in polymerization and hydrolyzed to form Si–O–Si cross-linked structure at the later stage. The obtained microspheres are not only highly cross-linked but also have uniform particle size distribution and good thermal stability. The produced cross-linked PMMA microspheres exhibit great light diffusion properties and might be employed as a light diffusion agent in a polycarbonate matrix. We prepared the cross-linked PMMA microspheres by post-crosslinking method and mixed the cross-linked PMMA microspheres with the matrix PC to obtain the light diffusers. [ABSTRACT FROM AUTHOR]

Cross-linked poly(methyl methacrylate) (PMMA) microspheres have been successfully prepared by using the asymmetric cross-linker allyl methacrylate (AMA) via dispersion polymerization. The influence of the AMA amount and polymerization process on the PMMA particle size and morphology has been studied thoroughly. It was found that micron-sized, cross-linked PMMA particles with narrow size distributions could be obtained by a semi-continuous process with the asymmetric cross-linker AMA. The obtained micron-sized, cross-linked PMMA particles could be further used as a light diffusion agent in a polycarbonate matrix, and their light diffusion properties were significantly enhanced by increasing the gel content in the cross-linked particles. Moreover, the influence of the polymerization process, cross-linker content in PMMA and PMMA content in the polycarbonate matrix on light diffusion was carefully investigated. The results showed that the PMMA particles containing 5.0 wt% AMA, obtained by semi-continuous polymerization, had a higher haze and gel content and exhibited a better light diffusion effect than did the other particles. [ABSTRACT FROM AUTHOR]

Nanoscale poly(alkyl methacrylate)s including poly(methyl methacrylate), poly(ethyl methacrylate), poly(cyclohexyl methacrylate), poly(iso-butyl methacrylate) and poly(benzyl methacrylate) were prepared by a modified microemulsion polymerization procedure. NMR analysis suggested that these poly(methacrylate)s samples were higher in syndiotactic content, lower in isotactic content and the glass transition temperatures (Tgs) of them were also higher than those reported in the literature. The tacticities of the poly(methacrylate)s, beside the restricted volume effect of nanoparticles during the modified microemulsion polymerization, were mainly influenced by the reaction temperature, the lower the reaction temperature, the higher the syndiotacticity of the products. The syndiotacticity of the product decreased obviously when the polymerization was carried out at a temperature far above the Tg of the resulting polymer. It was also shown that the tacticity of the polymer was affected by the monomer structure, a monomer with the bulkier alkyl side group would liable to result in a polymer with richer syndiotacticity. Possible mechanism of rich-syndiotacticity was also discussed. [ABSTRACT FROM AUTHOR]

Semi-transparent reactive microgel in nanosize has been prepared by modified microemulsion polymerization using a common emulsifier, crosslinking agent and functional monomer. The microgels are translucent reactive nanoparticles, with the size of 40–100 nm, consisting of inner-crosslinked polymer up to 40%. FT-IR proved the functional groups, such as epoxy and hydroxy, are on the surface of the microgel nanoparticles. Rheological detection demonstrated the apparent pseudoplasticity of the non-aqueous microgel dispersion prepared by the phase transfering from the O/W microlatexes. [ABSTRACT FROM AUTHOR]

Abstract: Monte Carlo simulation of chemically reacting systems based on the master equation was used to describe the stochastic time evolution of the microemulsion polymerization system. A model was developed to demonstrate its applicability for hexyl methacrylate and styrene microemulsion polymerization. The properties of final latex, such as the particle size and molecular weight distributions were obtained simultaneously. The polymerization behavior and properties of final latexes were well reproduced. The model is valuable in confirming or elucidating the various mechanisms in the polymerization. The entry and desorption mechanism was well established to account for the polymerization kinetics. The general polymerization behavior of hydrophobic monomer in microemulsions was properly simulated by the model proposed. [Copyright &y& Elsevier]

Abstract: A novel luminescent nanocomposite assembly was prepared in aqueous solutions, via the electrostatic interaction between poly(ethylene glycol)-b-poly(-dimethylaminoethyl methacrylate) (PEG-b-PDMAEMA) double hydrophilic block copolymer (DHBC) and thioglycolic acid (TGA)-stabilized CdTe quantum dots (QDs). By tuning the molar ratios of QDs to DHBC, the nanocomposite assemblies could be well controlled and the dimension of these regular spherical QDs/PEG-b-PDMAEMA assemblies ranged from 40 to 75 nm in aqueous media. As the periphery of QDs/PEG-b-PDMAEMA nanocomposite assembly was composed of PEG segments when the PDMAEMA blocks and QDs were immobilized inside the assembly, the cytotoxicity of the assembly was significantly reduced, compared with that of pure PEG-b-PDMAEMA and QDs. The nanocomposite assembly also exhibited superior stability in salt solutions and remained strongly photoluminescent even when free radicals existed. Thus, the QDs/PEG-b-PDMAEMA nanocomposite assembly is potentially useful for a number of applications in biolabeling and imaging. [Copyright &y& Elsevier]