A rapid synthesis of nanofibrillar cellulose/polystyrene composite via ultrasonic treatment.

A new method of the synthesis of nanofibrillar cellulose/polystyrene composite based on ultrasonic treatment of styrene emulsion in cellulose-water solution was elaborated. A new approach does not require additional heating and proposes a significantly faster synthesis (15 min, 45 °C) of the target composite compared to the methods described previously. A comprehensive analysis did not reveal any significant differences between mechanical, physical and biodegradable properties of the composite obtained by ultrasonic method and that one obtained by conventional thermal method, which requires much higher temperature (above 75 °C) and reaction duration (from 3 h).

Nanocontainer-Based Active Systems: From Self-Healing Coatings to Thermal Energy Storage.

We highlight the development of nanocontainer-based active materials started in 2006 at the Max Planck Institute of Colloids and Interfaces under the supervision of Prof. Helmuth Möhwald. The active materials encapsulated in the nanocontainers with controlled shell permeability have been first applied for self-healing coatings with controlled release of the corrosion inhibitor. The nanocontainers have been added to the paint formulation matrix at 5-10 wt % concentration, which resulted in attaining a coating-autonomous self-healing ability. This research idea has attracted the attention of many scientists around the world (>1500 publications during the last 10 years) and has already been transferred to the commercialization level. The current trend in nanocontainer-based active systems is devoted to the multifunctionality of the capsules which can combine self-healing, antibacterial, thermal, and other functionalities into one host matrix. This article summarizes the previous research done in the area of nanocontainer-based active materials together with future perspectives of capsule-based materials with antifouling or thermoregulating activity.

Nanoencapsulation of phase change materials for advanced thermal energy storage systems.

Phase change materials (PCMs) allow the storage of large amounts of latent heat during phase transition. They have the potential to both increase the efficiency of renewable energies such as solar power through storage of excess energy, which can be used at times of peak demand; and to reduce overall energy demand through passive thermal regulation. 198.3 million tons of oil equivalent were used in the EU in 2013 for heating. However, bulk PCMs are not suitable for use without prior encapsulation. Encapsulation in a shell material provides benefits such as protection of the PCM from the external environment and increased specific surface area to improve heat transfer. This review highlights techniques for the encapsulation of both organic and inorganic PCMs, paying particular attention to nanoencapsulation (capsules with sizes <1 µm). We also provide insight on future research, which should focus on (i) the development of multifunctional shell materials to improve lifespan and thermal properties and (ii) advanced mass manufacturing techniques for the economically viable production of PCM capsules, making it possible to utilize waste heat in intelligent passive thermal regulation systems, employing controlled, "on demand" energy release/uptake.

Bioinspired nanovalves with selective permeability and pH sensitivity.

Biological systems with controlled permeability and release functionality, which are among the successful examples of living beings to survive in evolution, have attracted intensive investigation and have been mimicked due to their broad spectrum of applications. We present in this work, for the first time, an example of nuclear pore complexes (NPCs)-inspired controlled release system that exhibits on-demand release of angstrom-sized molecules. We do so in a cost-effective way by stabilizing porous cobalt basic carbonates as nanovalves and realizing pH-sensitive release of entrapped subnano cargo. The proof-of-concept work also consists of the establishment of two mathematical models to explain the selective permeability of the nanovalves. Finally, gram-sized (or larger) quantities of the bio-inspired controlled release system can be synthesized through a scaling-up strategy, which opens up opportunities for controlled release of functional molecules in wider practical applications.

Characterization of micro- and nanocapsules for self-healing anti-corrosion coatings by high-resolution SEM with coupled transmission mode and EDX.

The observation of morphological details down to the nanometer range of the outer surface of micro-, submicro- and nanoparticles in a high-resolution scanning electron microscope (SEM) was extended with in-depth observation by enabling the transmission mode in the SEM, i.e. TSEM. The micro- and nanocapsules characterized in this study were fabricated as depots for protective agents to be embedded in innovative self-healing coatings. By combining the two imaging modes (upper and in-depth observation) complementing each other a better characterisation by a more comprehensive interpretation of the "consistency" of the challenging specimens, e.g. including details "hidden" beyond the surface or the real specimen shape at all, has been attained. Furthermore, the preparation of the quasi electron transparent samples onto thin supporting foils enables also elemental imaging by energy dispersive X-ray spectroscopy (EDX) with high spatial resolution. Valuable information on the elemental distribution in individual micro-, submicro- and even nanocapsules completes the "3D" high resolution morphological characterization at the same multimodal SEM/TSEM/EDX system.

Evaluation of the role of polyelectrolyte deposition conditions in growth factor release.

Polyelectrolyte multilayer coatings were prepared from solutions of poly(methacrylic acid) and poly-l-histidine. Bone morphogenetic protein 2 (BMP-2) was adsorbed onto the surface of anodized titanium and polyelectrolyte multilayer coatings were built up on top of the BMP-2. The effect of deposition conditions on coating properties and preosteoblast response was measured by comparing coatings prepared under natural conditions to those prepared from solutions at pH = 6.0 and solutions containing 0.1 M NaCl. High levels of BMP-2 release were achieved, with coatings prepared from pH = 6.0 solutions releasing 86 ng cm-2 and coatings prepared from solutions containing 0.1 M NaCl releasing 114 ng cm-2 over 25 days. Enhanced preosteoblast differentiation was observed on coatings prepared from modified solutions; however, this increased differentiation was apparent for BMP-2-eluting and control coatings. Additionally, a positive relationship between surface roughness and differentiation was observed, which may account for increased differentiation for systems that do not release BMP-2.

Polyelectrolyte multilayered nanofilms as a novel approach for the protection of hydrogen storage materials.

This work describes the encapsulation of hydrogen storage materials from organic solvents. Due to complex formation the shell provides stability and selective permeability. Specifically, sodium borohydride particles were encapsulated within polymer films by the layer-by-layer self-assembly of oppositely charged polyelectrolytes (polyethyleneimine and poly(acrylonitrile-co-butadiene-co-acrylic acid)). The polymer nanofilm fabrication was performed using dichloromethane as a working media. IR spectroscopy was applied to investigate the chemical interaction between the polyelectrolytes. The multilayer film preparation was verified by Z-potential measurements, scanning electron microscopy, and confocal laser microscopy. The stability of sodium borohydride protected with a polyelectrolyte shell was increased compared to that of the pure material under ambient conditions.

Theoretical evaluation of nano- or microparticulate contact angle at fluid/fluid interfaces: analysis of the excluded area behavior upon compression.

A novel method for the determination of the particle contact angle at the liquid/gas or liquid/liquid interface based on the excluded area concept revealed, in spite of its simplicity, some serious difficulties connected with the exact quantitative particle deposition at the interface and with changes in the particulate contact angle upon binary monolayer compression. The comprehensive theoretical consideration of the contact angle behavior made for such a system allowed considerable improvements: firstly, the prediction of direction of the particles' displacement at surface pressure increase is now possible and hence an unambiguous identification of particle hydrophobicity can be done. Secondly, the analytical relation describing the dependence of the particulate contact angle on the surface tension (surface pressure) was derived, allowing the prediction of whether or not particles of a given hydrophobicity will be expelled from the monolayer at certain surface pressure and of the area relinquished by the displaced particles. Thirdly, the transformation of this relation upon taking into consideration the initial conditions led to a linear dependence between excluded area and normalized surface tension allowing the determination of the particle contact angle and the exact number of deposited particles simultaneously and independently of each other. Finally, the application of the improved approach to the previously collected experimental data yielded reasonable values for both particle contact angle and number of deposited particles.

New method for fabrication of loaded micro- and nanocontainers: emulsion encapsulation by polyelectrolyte layer-by-layer deposition on the liquid core.

A novel approach to the emulsion encapsulation was developed by combining the advantages of direct encapsulation of a liquid colloidal core with the accuracy and multifunctionality of layer-by-layer polyelectrolyte deposition. Experimental data obtained for the model oil-in-water emulsion confirm unambiguously the alternating PE assembly in the capsule shell as well as the maintenance of the liquid colloidal core. Two different mechanisms of capsule destruction upon interaction with the solid substrate were observed and qualitatively explained. The proposed method can be easily generalized to the preparation of oil-filled capsules in various oil/water/polyelectrolyte systems important in the field of pharmacy, medicine, and food industry.