Interaction of Cationic, Anionic, and Nonionic Macroraft Homo- and Copolymers with Laponite Clay.

The functionalization of Laponite RD platelets with different cationic, anionic, and nonionic homo- and copolymers synthesized by reversible addition-fragmentation chain transfer (RAFT) has been investigated. The effective interaction of the macromolecular RAFT agents (macroRAFTs) with the inorganic particles is known to be of crucial importance for the successful coating of minerals with polymers via RAFT-mediated emulsion polymerization to produce polymer-encapsulated inorganic particles. The macroRAFT agents synthesized in the present work contain carefully selected reinitiating R groups, which bear either ionizable tertiary amine or quaternary ammonium moieties (from 2-(dimethylamino)ethyl methacrylate, DMAEMA), negatively charged acrylic acid (AA) repeat units, or neutral polyethylene glycol (PEG) side chains, and are capable of interacting with Laponite via different adsorption mechanisms. The equilibrium adsorption of these RAFT (co)polymers was investigated by the plotting of adsorption isotherms, and either L-type or H-type curves were obtained. The hydrophobicity of the macroRAFT was shown to promote adsorption, as did the pending configuration of the PEG block. Charge repulsion between AA and the negatively charged surface of Laponite at pH 7.5, on the other hand, was prejudicial for adsorption, while the strong electrostatic interaction between the cationic DMAEMA molecules and the Laponite surface led to high-affinity-type curves.

Investigation of the Adsorption of Amphipathic macroRAFT Agents onto Montmorillonite Clay.

Recently, there has been significant interest in the use of the reversible addition-fragmentation chain-transfer (RAFT) technique to generate a variety of organic/inorganic colloidal composite particles in aqueous dispersed media using the so-called macroRAFT-assisted encapsulating emulsion polymerization (REEP) strategy. In this process, special attention should be paid to the adsorption of the macromolecular RAFT (macroRAFT) agent onto the inorganic particles, as it determines the final particle morphology and can also influence latex stability. In this work, different amphipathic macroRAFT agents were synthesized by RAFT, and their adsorption onto commercial Montmorillonite clay Cloisite Na+ (MMT) was studied by means of adsorption isotherms. Three types of macroRAFT agents were considered: a nonionic one based on poly(ethylene glycol) methyl ether acrylate (PEGA) and n-butyl acrylate (BA), anionic ones, including a block copolymer and random copolymers, based on acrylic acid (AA), BA and PEGA, and cationic ones based on 2-(dimethylamino)ethyl methacrylate (DMAEMA), BA and PEGA. Six adsorption isotherm models (Langmuir, Freundlich, Tempkin, Redlich-Peterson, Sips, and Brunauer-Emmett-Teller) were adjusted to the experimental isotherms. The nonionic macroRAFT agent formed a monolayer on the clay surface with a maximum adsorption capacity of 400 mg g-1 at pH 8, as determined from the Sips adsorption model. Adsorption of the AA-based macroRAFT agents onto MMT was moderate at alkaline pH due to electrostatic repulsions, but increased with decreasing pH. The DMAEMA-based macroRAFT agents displayed a much stronger interaction with the oppositely charged MMT surface at acidic pH due to electrostatic interactions, and the concentration of adsorbed macroRAFT agent reached values as high as 800 mg g-1. The BET model fitted the experimental data relatively well indicating multilayer adsorption promoted by the presence of the hydrophobic BA units. In addition, the cationic macroRAFT agents afforded stable MMT/macroRAFT agent complexes as evaluated by dynamic light scattering and zeta potential analyses.

Langmuir monolayers of fractions of cork suberin extract.

The wide variability in composition and molecular weight of natural polymers has hampered understanding of their physicochemical properties and ultimately their use in noble applications, especially in the cases where surface properties need to be probed at the molecular level. A useful approach to analyse data from surface monolayers of complex mixtures is to try distinguishing the effects from the distinct fractions in such mixtures. The cork suberin extract investigated here is known to contain aliphatic monomers with terminal carboxylic acid and methyl ester groups as well as long esterified aliphatic chains dispersed in a polymeric aliphatic matrix. The role of such terminal groups was studied and the results showed that depending on the nature of the terminal groups the monolayers present distinct isotherms due to the different interactions with the water subphase. Fractionation strategies based on different solubilities of the cork suberin components in chloroform were also employed to probe their effect on the monolayer characteristics. From the two sets of experiments it is clear that the presence of monomers with terminal carboxylic acids in the suberin extract affects considerably the monolayer-forming ability. This approach may be used as a complementary, relatively simple route to assess suberin genetic engineering strategies towards resistance to environmental stress.

Cell surface characterization of Yarrowia lipolytica IMUFRJ 50682.

In the present work, the surface characteristics of a wild-type strain of Yarrowia lipolytica (IMUFRJ50682) were investigated. Six different methods to characterize cell surfaces--adhesion to polystyrene; hydrophobic interaction chromatography (HIC); microbial adhesion to solvents (MATS) test; zeta potential; microbial adhesion to hydrocarbons (MATH) test; and contact angle measurement (CAM)--were employed to explain the cell surface behaviour of Y. lipolytica (IMUFRJ50682). This Y. lipolytica strain presents significant differences at the cell surface compared with another Y. lipolytica strain (W29) previously reported in the literature. The main difference is related to the higher cell adhesion to non-polar solvents. The proteins present on the cell wall of Y. lipolytica IMUFRJ50682 seem to play an important role in these particular surface characteristics because of the consistent reduction of this yeast hydrophobic character after the action of pronase on its cell wall.

Synthesis of SiO2-coated Bi2S3/poly(styrene) nanocomposites by in-situ polymerization.

New nanocomposites containing silica-coated Bi2S3 nanofibers were synthesised by in situ polymerization using two distinct synthetic strategies: emulsion and suspension polymerization. Transmission and scanning electron microscopy of the nanocomposite particles showed that in both cases the Bi2S3/SiO2 nanoparticles were densely coated with poly(styrene). In situ emulsion polymerization afforded nanocomposites in which the nanofibers were coated with polymer spheres whilst suspension polymerization gives rise to a homogeneous polymer layer coat. The morphology of the poly(styrene) coating observed is discussed considering the surface modification of the nanofibers and the polymerization technique involved.

Polymer encapsulation of CdE (E = S, se) quantum dot ensembles via in-situ radical polymerization in miniemulsion.

Cadmium sulfide and cadmium selenide/polymer nanocomposites were prepared via in-situ radical polymerization in miniemulsion. Organically capped CdE (E = S, Se) quantum dots (QDs) were used as the starting materials and ensembles of these dots were encapsulated with no need of further surface treatment. The use of two polymer matrices was investigated: polystyrene (PS) and poly(n-butyl acrylate) (PBA). In both cases, homogenous nanocomposites were obtained and their optical properties were investigated by visible absorption and photoluminescence spectroscopy. Quantum size effects were assigned to the nanocomposites, indicating the integrity of the individual QDs upon polymer encapsulation using the miniemulsion process.

Oxypropylation of cork and the use of the ensuing polyols in polyurethane formulations.

Cork particles, recovered as byproducts of the processing of this natural material, were oxypropylated under pressure and relatively high temperature in the presence of KOH as catalyst. Various parameters were explored in order to assess the most suitable conditions, which led to the almost complete conversion of the solid cork into a viscous polyol. This product was a mixture of oxypropylated cork macromolecules and propylene oxide oligomers, which were thoroughly characterized. The use of these polyols as macromonomers in the synthesis of polyurethane foams gave promising results, thus showing that it should be possible to exploit the residues of this important renewable resource to manufacture original materials.