3 research outputs found

    Electrostatic Interactions and Osmotic Pressure of Counterions Control the pH-Dependent Swelling and Collapse of Polyampholyte Microgels with Random Distribution of Ionizable Groups

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    In this work, different systems of colloidally stable, ampholytic microgels (μGs) based on poly­(<i>N</i>-vinyl­capro­lactam) and poly­(<i>N</i>-isopropyl­acryl­amide), wherein the anionic and cationic groups are randomly distributed, were investigated. Fourier transmission infrared spectroscopy and transmission electron microscopy confirmed the quantitative incorporation and random distribution of ionizable groups in μGs, respectively. The control of hydrodynamic radii and mechanical properties of polyampholyte μGs at different pH values was studied with dynamic light scattering and in situ atomic force microscopy. We have proposed a model of pH-dependent polyampholyte μG, which correctly describes the experimental data and explains physical reasons for the swelling and collapse of the μG at different pHs. In the case of a balanced μG (equal numbers of cationic and anionic groups), the size as a function of pH has a symmetric, V-like shape. Swelling of purely cationic μG at low pH or purely anionic μG at high pH is due to electrostatic repulsion of similarly charged groups, which appears as a result of partial escape of counterions. Also, osmotically active counterions (the counterions that are trapped within the μG) contribute to the swelling of the μG. In contrast, electrostatic interactions are responsible for the collapse of the μG at intermediate pH when the numbers of anionic and cationic groups are equal (stoichiometric ratio). The multipole attraction of the charged groups is caused by thermodynamic fluctuations, similar to the those observed in Debye–Hückel plasma. We have demonstrated that the higher the fraction of cationic and anionic groups, the more pronounced the swelling and collapse of the μG at different pHs

    Das Susac Syndrom - Mikroangiopathie als seltene Ursache bilateraler Taubheit

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    We report on the behavior of two immiscible liquids within polymer microgel adsorbed at their interface. By means of dissipative particle dynamics (DPD) simulations and theoretical analysis in the framework of the Flory–Huggins (FH) lattice theory, we demonstrate that the microgel acts as a “compatibilizer” of these liquids: their miscibility within the microgel increases considerably. If the incompatibility of the liquids is moderate, although strong enough to induce phase separation in their 1:1 composition, they form homogeneous mixture in the microgel interior. The mixture of highly incompatible liquids undergoes separation into two (micro)­phases within the microgel likewise out of it; however, the segregation regime is weaker and the concentration profiles are characterized by a weaker decay (gradient) in comparison with those of two pure liquids. The enhanced miscibility is a result of the screening of unfavorable interactions between unlike liquid molecules by polymer subchains. We have shown that better miscibility of the liquids is achieved with densely cross-linked microgels. Our findings are very perspective for many applications where immiscible species have to be mixed at interfaces (like in heterogeneous catalysis)

    Swelling of a Responsive Network within Different Constraints in Multi-Thermosensitive Microgels

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    We report on the swelling of a polymeric network in doubly thermoresponsive microgels. Silica-core double-shell and hollow double-shell microgels made of an inner poly­(<i>N</i>-isopropyl­methacrylamide) and an outer poly­(<i>N</i>-isopropyl­acrylamide) shell are studied by exploiting the distinct temperature sensitivities of the polymers. The swelling states of the two shells can be tuned by temperature changes enabling three different swelling states: above, below, and between the distinct volume phase transition temperatures of the two polymers. This enables to investigate the effect of different constraints on the swelling of the inner network. Small-angle neutron scattering with contrast variation in combination with computer simulation discloses how the expansion of the inner shell depends on the material and swelling state of its constraints. In the presence of the stiff core, the microgels show a considerable interpenetration of the polymeric shells: the inner network expands into the outer deswollen shell. This interpenetration vanishes when the outer network is swollen. Furthermore, as predicted by our computer simulations, an appropriate choice of cross-linking density enables the generation of hollow double-shell nanocapsules. Here, the inner shell undergoes a <i>push–pull effect</i>. At high temperature, the collapsed outer shell pushes the swollen inner network into the cavity. At lower temperature, the swelling of the outer network contrary pulls the inner shell back toward the external periphery
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