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Polymer hydrogels are known to be efficient absorbents of various aqueous solutions. Along with the hydrophilicity of the polymer network, the presence of specific functional groups is required for the absorption of respective solutes. Alternatively, a selective uptake can be realized without any specific attraction of solutes to the network, which is shown in this paper. By combining experimental and simulation approaches, we demonstrated that thermoresponsive poly( N -isopropylacrylamide) gels and microgels in compositionally strongly asymmetric water/1-octanol mixtures selectively uptake the minor (1-octanol) component. Initially swollen in water, the gels substitute water by the organic solvent upon the addition of its small fraction into aqueous solution. In turn, for microgels, it was shown that the single particles could absorb the amount of the organic liquid more than two times higher than their mass while preserving the colloidal stability. At the same time, the accumulation of 1-octanol in the networks "switches off" the temperature response. The mesoscopic computer simulations revealed a physical reason and molecular picture of the phenomenon. Absorption of the minor component by the gels is caused by the decrease in water/1-octanol interfacial tension due to the formation of the dense polymer layer at the interface. The simulations allowed tracking the evolution of the size and the internal structure of the single microgels with changing 1-octanol concentration.

It is known that microgels can serve as soft, permeable and stimuli-responsive alternative of solid colloidal particles to stabilize oil-water emulsions. The driving force for the adsorption of the microgels on interface of two immiscible liquids is a shielding of unfavorable oil-water contacts by adsorbed subchains, that is, the decrease of the surface tension between the liquids. Such phenomenon usually proceeds if volume fractions of the two liquids are comparable with each other and the microgel concentration is not high enough. The natural question arises: what is going on with the system in the opposite case of strongly asymmetric mixture (one of the liquids (oil) has a very small fraction) or high microgel concentration (the overall volume of the microgels exceeds the volume of the minor oil component)? Here we demonstrate that the microgels uptake the oil whose concentration within the microgels can be orders of magnitude higher than outside, leading to the additional microgel swelling (in comparison with the swelling in water). Thus, the microgels can serve as scavengers and concentrators of liquids dissolved in water. At first glance, this effect seems counterintuitive. However, it has a clear physical reason related to the incompatibility of oil and water. Absorption of the oil by microgels reduces unfavorable oil-water contacts by microgel segments: the microgels have a higher concentration of the segments at the periphery, forming a shell. The microgels with uptaken oil are stable toward aggregation at very small oil concentration in the mixture. However, an increase in the oil concentration can lead to aggregation of the microgels into dimers, trimers, and so on. The increasing concentration of oil mediates the attraction between the microgels: the oil in the aggregates appears to be localized in-between the microgels instead of their interior, which is accompanied by the release of the elastic stress of the microgels. A further increase in the oil concentration results in a growth of the size of the oil droplets between the microgels and the number of the microgels at the droplet's periphery, that is, the emulsion is formed.

Exploring and controlling chemical reactions in compartments opens new platforms for designing bioinspired catalysts and energy-autonomous systems. Aqueous polymer networks or hydrogels serve as a perfect model for biological tissues, allowing systematic investigations of chemical transformations in compartments. Herein, we report the synthesis of a versatile, colloidal microgel catalyst containing covalently bound l-proline as an organocatalyst. The key finding of our work is that the catalytic activity can be tuned by adjusting the distribution of the organocatalyst in the microgel network as well as the properties of the solvent. We demonstrate that l-proline groups integrated into microgels enable the reaction of 4-nitrobenzaldehyde and cyclohexanone in a heterogeneous reaction mixture in which free l-proline is not active. By controlling the localization of the l-proline groups within the microgel network (core or corona), the rate of the aldol reaction in homogenous and heterogeneous reaction mixtures can be modulated. Furthermore, microgels with covalently attached catalysts can be recycled and reused in sequential catalytic runs without deterioration of the catalyst performance in terms of activity and selectivity. The internal structure of the microgel in heterogeneous reaction mixtures was studied by computer simulations., (Copyright © 2019 Elsevier Inc. All rights reserved.)