Stefanie Schneider

Unperturbed volume transition of thermosensitive poly-(N-isopropylacrylamide) microgel particles embedded in a hydrogel matrix.

The thermoresponsive behavior of poly-(N-isopropylacrylamide) (PNiPAM) microgels embedded in a covalently cross-linked polyacrylamide hydrogel matrix was investigated using ultraviolet-visible (UV-vis) spectroscopy, small-angle neutron scattering (SANS), and confocal laser scanning microscopy. The hydrogel synthesis was performed at two different temperatures, below and above the volume phase transition temperature of PNiPAM, resulting in highly swollen or fully collapsed PNiPAM microgel particles during the incorporation step. UV-vis spectroscopy experiments verify that the incorporation of thermosensitive microgels leads to temperature-sensitive optical properties of the composite materials. SANS measurements at different temperatures show that the thermosensitive swelling behavior of the PNiPAM microgels is fully retained in the composite material. Volume and structure criteria of the embedded microgel particles are compared to those of the free microgels in acrylamide solution. To visualize the temperature responsive behavior of larger PNiPAM particles, confocal fluorescence microscopy images of PNiPAM beads, of 40-microm size, were taken at two different temperatures. The micrographs also demonstrate the retained temperature sensitivity of the embedded microgels.

Balancing Segregation and Complexation in Amphiphilic Copolymers by Architecture and Confinement

Segregation is a well-known principle for micellization, as solvophobic components try to minimize interactions with other entities (such as solvent) by self-assembly. An opposite principle is based on complexation (or coacervation), leading to the coassembly/association of different components. Most cases in the literature rely on only one of these modes, though the classical micellization scheme (such as spherical micelles, wormlike micelles, and vesicles) can be enriched by a subtle balance of segregation and complexation. Because of their counteraction, micellar constructs with unprecedented structure and behavior could be obtained. In this feature, systems are highlighted, which are between both mechanisms, and we study concentration, architecture, and confinement effects. Systems with inter- and intramolecular interactions are presented, and the effects of polymer topology and monomer sequence on the resulting structures are discussed. It is shown that complexation can lead to altered micellization behavior as the complex of one hydrophobic and one hydrophilic component can have a very low surface tension toward the solvent. Then, the more soluble component is enriched at the surface of the complex and acts as a microsurfactant. Although segregation dominates for amphiphilic copolymers in solution, the effect of the complexation can be enhanced by branching (change of architecture). Another possibility to enhance the complexation is by confining copolymers in a (pseudo-) 2D environment (like the one available at liquid-liquid interfaces). These observations show how new structural features can be achieved by tuning the subtle balance between segregation and complexation/solubilization.

Optimal Displacement Parameters in Monte Carlo Simulations

An adaptive algorithm optimizing single-particle translational displacement parameters in Metropolis Monte Carlo simulations is presented. The optimization is based on maximizing the mean square displacement of a trial move. It is shown that a large mean square displacement is strongly correlated with a high precision of average potential energy. The method is here demonstrated on model systems representing a Lennard-Jones fluid and a dilute polymer solution at poor solvent conditions. Our adaptive algorithm removes the need to provide values of displacement parameters in simulations, and it is easily extendable to optimize parameters of other types of trial moves.

Monte Carlo simulations of weak polyelectrolyte microgels: pH-dependence of conformation and ionization

In this study, we investigated the effect of pH on single weak acidic polyelectrolyte microgels under salt-free conditions with (i) varying microgel concentration, (ii) varying content of acidic groups and (iii) different crosslinking densities using Monte Carlo simulations under explicit consideration of the protonation/deprotonation reaction. We assessed both global properties, such as the degree of ionization, the degree of swelling and the counterion distribution, and local properties such as the radial network ionization profile and the ionization along the polymer chains as a function of pH. We found a pronounced suppression of the pH-dependent ionization of the microgels, as compared to the ideal titration behavior and a shift of the titration curve to a higher pH originating in the proximity of acidic groups in the microgel. In contrast to macroscopic gels, counterions can leave the microgel, resulting in an effective charge of the network, which hinders the ionization. A decreasing microgel concentration leads to an increased effective charge of the microgel and a more pronounced shift of the titration curve. The number of acidic groups showed only a weak effect on the ionization behavior of the microgels. For two different microgels with different crosslinking densities, similar scaling of the gel size was observed. A distinct transition from an uncharged and unswollen to a highly charged and expanded polymer network was observed for all investigated microgels. The degree of swelling mainly depends on the degree of ionization. An inhomogeneous distribution of the degree of ionization along the radial profile of the microgel was found.

Spacer Chains Prevent the Intramolecular Complexation in Miktoarm Star Polymers

The influence of spacer chains on the intramolecular complexation in star-shaped heteroarm (miktoarm) polymers is investigated. To overcome the mutual attraction of different polymeric components present in a miktoarm star with different homopolymeric arms, spacer chains of different length are attached to the core of the star at three different positions. In most of the investigated cases, this leads to diblock copolymer arms within the miktoarm star. Hereby, the inner spacer separates the outer blocks from their attractively interacting homopolymeric arms. The effect on the intramolecular complexation and the structure of the star polymer is obtained by Monte Carlo simulations of a simple bead-spring model. Then, long spacers can completely prevent the complexation. Both, local shielding by the spacer chains and the increased distance between the complex-forming polymers due to the spacer chains inhibit the complex formation. For a range of spacer positions and lengths, an equilibrium between a system forming a complex and a complex free system is found. The spacer chains can be used as a tool to tune the intramolecular complexation.