Nanoscale Structures of Tough Microparticle-Based Films Investigated by Synchrotron X-Ray Scattering and All-Atom Molecular-Dynamics Simulation.

In this study, the nanoscale structures of microparticle-based films are revealed by synchrotron small-angle X-ray scattering (SAXS) and all-atom molecular-dynamics (AA-MD) simulations. The microparticle-based films consisting of the simplest acrylate polymer microparticles are applied as a model because the films are formed without additives and organic solvents and exhibit high toughness properties. The characteristic interfacial thickness () obtained from the SAXS analysis reflects the mixing degree of polymer chains on the microparticle surface in the film.

Nanoparticle-Based Tough Polymers with Crack-Propagation Resistance.

Although thin elastomer films of polymer nanoparticles are regarded as environmentally friendly materials, the low mechanical strength of the films limits their use in various applications. In the present study, we investigated the fracture resistance of latex films composed of acrylic nanoparticles where a small quantity of a rotaxane crosslinker was introduced. In contrast to conventional nanoparticle-based elastomers, the latex films composed of the rotaxane-crosslinked nanoparticles exhibited unusual crack propagation behavior; the direction of crack propagation changed from a direction parallel to the crack to one perpendicular to the crack, resulting in an increase in tear resistance.

Controlling the mechanical properties of hydrogels modulating the side-chain length.

Even though the toughness of hydrogels is usually adjusted by changing the cross-linking density and structure, or the polymer concentration, we have discovered a new strategy to control the toughness modulating the side-chain length. In this study, this strategy was applied to biocompatible poly(oligo(ethylene glycol) methyl ether methacrylate) with long ethylene-oxide side chains.

Nanostructure and thermoresponsiveness of poly(-isopropyl methacrylamide)-based hydrogel microspheres prepared aqueous free radical precipitation polymerization.

Thermoresponsive hydrogel microspheres (microgels) are smart materials that quickly respond to external stimuli, and their thermoresponsiveness can be tuned by varying the constituent chemical species. Although uniformly sized microgels can be prepared aqueous free radical precipitation polymerization, the nanostructure of the obtained microgels is complex and remains unclear so far. In the present study, the nanostructure and thermoresponsiveness of poly(-isopropyl methacrylamide) (pNIPMAm)-based microgels, which have a volume-transition temperature of ∼43 °C, were evaluated mainly using temperature-controllable high-speed atomic force microscopy.

Mechanical properties of temperature-responsive gels containing ethylene glycol in their side chains.

The mechanical properties of temperature-responsive and biocompatible poly(oligo-ethylene glycol methyl ether methacrylate)-based gels were investigated using dynamic viscoelasticity measurements so as to find applications in tissue and biomedical engineering. The gels were copolymerized using two ethylene glycol methacrylate monomers with diethylene glycol side chains: diethylene glycol methacrylate (MeOMA), which contains two ethylene oxide units, and oligo-ethylene glycol methyl ether methacrylate (OEGMA) with either four or five ethylene oxide units. The storage (G') and loss (G'') moduli of these gels exhibit unique temperature-responsive behavior and depend on the copolymerization ratio.

Concentration dependence of the dynamics of microgel suspensions investigated by dynamic light scattering.

The dynamics of colloidal gel particle suspensions, i.e., microgel suspensions, has been investigated by dynamic light scattering (DLS) over a wide concentration range from the (I) dilute (φ < φcp) to the (II) intermediate (φ ≈ φcp) and (III) high concentration regions (φ ≫ φcp), where φ and φcp are the volume fraction of the gel particles in the suspension and the random close packing fraction, φcp ≈ 0.

Non-Thermoresponsive Decanano-sized Domains in Thermoresponsive Hydrogel Microspheres Revealed by Temperature-Controlled High-Speed Atomic Force Microscopy.

Despite the tremendous efforts devoted to the structural analysis of hydrogel microspheres (microgels), many details of their structures remain unclear. Reported in this study is that thermoresponsive poly(N-isopropyl acrylamide) (pNIPAm)-based microgels exhibit not only the widely accepted core-shell structures, but also inhomogeneous decanano-sized non-thermoresponsive spherical domains within their dense cores, which was revealed by temperature-controlled high-speed atomic force microscopy (TC-HS-AFM). Based on a series of experiments, it is concluded that the non-thermoresponsive domains are characteristic for pNIPAm microgels synthesized by precipitation polymerization, and plausible structures for microgels prepared by other polymerization techniques are proposed.

Hydrogel Microellipsoids that Form Robust String-Like Assemblies at the Air/Water Interface.

Soft colloidal particles such as hydrogel microspheres assemble at air/water or oil/water interfaces, where the soft colloids are highly deformed and their surface polymer chains are highly entangled with each other. Herein, we report the formation of robust one-dimensional, string-like colloidal assemblies through self-organization of hydrogel microspheres with shape anisotropy at the air/water interface of sessile droplets. Shape-anisotropic hydrogel microspheres were synthesized via two-step polymerization, whereby a hydrogel shell was formed onto preformed rigid microellipsoids.

High Reusability of Catalytically Active Gold Nanoparticles Immobilized in Core-Shell Hydrogel Microspheres.

The reusability of hybrid core-shell microgels, whose core surfaces were decorated with gold nanoparticles, was investigated in terms of catalysis activity. Hybrid core-shell microgels composed of a rigid core and water-swollen gel shell endowed the immobilized gold nanoparticles with a high dispersion stability, which resulted in excellent catalytic activity. In contrast to free Au nanoparticles and conventional hybrid microgels, where the Au nanoparticles are randomly distributed over the entire microgel templates, the hydrogel shell part of the hybrid core-shell microgels suppressed the aggregation between the microgels and Au nanoparticles in individual microgels, which improved the reusability for the catalysis reaction.

Self-Organization of Soft Hydrogel Microspheres during the Evaporation of Aqueous Droplets.

The unique drying behavior of aqueous droplets that contain soft hydrogel microspheres (microgels) upon evaporation was systematically investigated. Compared to the ring-shaped deposits that are obtained from drying solid microsphere dispersions, we have previously reported that uniformly ordered thin films are obtained from drying ∼1.2 μm-sized poly( N-isopropyl acrylamide) microgel dispersions.

The deformation of hydrogel microspheres at the air/water interface.

The deformation of soft hydrogel microspheres (microgels) adsorbed at the air/water interface was investigated for the first time using large poly(N-isopropyl acrylamide)-based microgels synthesized by a modified aqueous precipitation polymerization method. The deformation of the micron-sized soft microspheres could be visualized clearly and analyzed quantitatively at the air/water interface.

Controlled Separation and Release of Organoiodine Compounds Using Poly(2-methoxyethyl acrylate)-Analogue Microspheres.

A selective adsorption/desorption of organoiodine compounds was achieved on poly(2-methoxyethyl acrylate)-analogue microspheres, wherein the side chains in the polymers act as halogen-bonding sites. These results demonstrate that the halogen-bonding sites in the side chains exhibit adequate specific affinity for organoiodine compounds. In addition, the water-swollen pMEA-analogue microspheres (microgels) showed a thermoresponsive swelling/deswelling behavior that permitted a controlled release of the organoiodine compounds upon changing the temperature.

Fast Adsorption of Soft Hydrogel Microspheres on Solid Surfaces in Aqueous Solution.

The real-time adsorption behavior of polymeric colloidal microspheres onto solid surfaces in aqueous solution was visualized for the first time using high-speed atomic force microscopy (HS-AFM) to reveal how the softness of the microspheres affects their dynamic adsorption. Studies that focus on the deformability of microspheres upon dynamic adsorption have not yet been reported, most likely on account of a lack of techniques that appropriately depict the dynamic adsorption and deformation behavior of individual microspheres at the nanoscale in real time. In this study, the deformability of microspheres plays a crucial role on the adsorption kinetics, that is, soft hydrogel microspheres adsorb faster than harder elastomeric or rigid microspheres.

Nanocomposite Microgels for the Selective Separation of Halogen Compounds from Aqueous Solution.

Nanocomposite microgels that selectively adsorb and release halogen compounds were developed. These nanocomposite microgels consist of poly(2-methoxyethyl acrylate) (pMEA) and a poly(oligo ethylene glycol methacrylate) hydrogel matrix. Therefore, the methoxy groups of the former are crucial for the halogen bonding, while the presence of the latter adds colloidal stability and allows controlled uptake/release of the halogen compounds.

Formation of Tough Films by Evaporation of Water from Dispersions of Elastomer Microspheres Crosslinked with Rotaxane Supramolecules.

Compared to rigid microspheres that consist, for example, of polystyrene or silica, soft and deformable elastomer microspheres can be used to generate colorless transparent films upon evaporating the solvent from microsphere-containing dispersions. To obtain tough films, a post-polymerization reaction to crosslink the microspheres is usually necessary, which requires extra additives during the drying process. This restriction renders this film-formation technology complex and rather unsuitable for applications in which impurities are undesirable.

Water-immiscible bioinert coatings and film formation from aqueous dispersions of poly(2-methoxyethyl acrylate) microspheres.

Poly(2-methoxyethyl acrylate) (pMEA) microspheres are prepared through facile free-radical polymerization in water without additives and impurities, such as surfactants, other polymers, and organic solvents, which are usually used to synthesize pMEA chains. Clean and pure (non-factionalized and non-cross-linking) pMEA microspheres exhibit plasma-protein adsorption resistances on their surface regardless of their charged state. They are characterized in terms of the adsorbed amounts of proteins at pH 7.

Impact of Spatial Distribution of Charged Groups in Core Poly(N-isopropylacrylamide)-Based Microgels on the Resultant Composite Structures Prepared by Seeded Emulsion Polymerization of Styrene.

A series of raspberry-shaped composite microgels were synthesized by seeded emulsion polymerization of styrene in the presence of hydrogel particles with different distributions of charged groups. Unlike microgels whose charged groups are localized in their center,29 polystyrene nanoparticles were formed inside the core microgels when the microgels whose charged groups were localized on their surface were used as cores for seeded emulsion polymerization. The effects of the surface charge densities of the core microgels and the concentration of styrene monomer during the polymerization on the resultant structures of composite microgels were investigated.

Investigation of Changes in the Microscopic Structure of Anionic Poly(N-isopropylacrylamide-co-Acrylic acid) Microgels in the Presence of Cationic Organic Dyes toward Precisely Controlled Uptake/Release of Low-Molecular-Weight Chemical Compound.

Changes in a microscopic structure of an anionic poly(N-isopropylacrylamide-co-acrylic acid) microgel were investigated using small- and wide-angle X-ray scattering (SWAXS). The scattering profiles of the microgels were analyzed in a wide scattering vector (q) range of 0.07 ≤ q/nm(-1) ≤ 20.

Localization of Polystyrene Particles on the Surface of Poly(N-isopropylacrylamide-co-methacrylic acid) Microgels Prepared by Seeded Emulsion Polymerization of Styrene.

Composite microgels with polystyrene nanoparticles were synthesized by seeded emulsion polymerization of styrene in the presence of pH- and temperature-responsive poly(N-isopropylacrylamide-co-methacrylic acid) microgels as seeds. In particular, the core microgels maintained their swelled state as the pH was increased to 10 during seeded emulsion polymerization conducted at an elevated temperature. Furthermore, we tuned the swelling degree of the core microgels at pH 10 by changing the amount of methacrylic acid incorporated during the synthesis of the core microgels.

Small-Angle X-ray Scattering Study on Internal Microscopic Structures of Poly(N-isopropylacrylamide-co-tris(2,2'-bipyridyl))ruthenium(II) Complex Microgels.

Internal microscopic structures of poly(N-isopropylacrylamide-co-tris(2,2'-bipyridyl))ruthenium(II) complex microgels were investigated using small-angle X-ray scattering (SAXS) in the extended q-range of 0.07 ≤ q/nm(-1) ≤ 20. The microgels were prepared by aqueous free-radical precipitation polymerization, resulting in formation of monodispersed, submicrometer-sized microgels, which was confirmed by transmission electron microscopy and dynamic light scattering.

Relationship between temperature-induced changes in internal microscopic structures of poly(N-isopropylacrylamide) microgels and organic dye uptake behavior.

Temperature-induced changes in the internal structures of poly(N-isopropylacrylamide) (pNIPAm) microgels were evaluated by small-angle X-ray scattering (SAXS), and the results were used to explain organic dye uptake by the microgels. The dye uptake experiments were conducted using two organic dyes: cationic rhodamine 6G (R6G) and anionic erythrosine. In the SAXS investigation, the internal structures of the microgels were characterized in terms of the correlation length, ξ, and the distance, d*, which originated from the local packing of the isopropyl groups of two neighboring chains.

Internal structures of thermosensitive hybrid microgels investigated by means of small-angle X-ray scattering.

Internal structures of thermosensitive microgels and their hybrid counterparts that contain Au nanoparticles are investigated by means of small-angle X-ray scattering (SAXS). Thermosensitive cationic microgels were synthesized by aqueous free radical precipitation polymerization from N-isopropylacrylamide and 3-(methacrylamino) propyltrimethylammonium chloride used as monomers. Using the microgels as templates, Au nanoparticles were synthesized in situ, using the cationic sites in the microgel to nucleate particle growth.