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Now showing 1 - 6 of 6
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    Self-Hydrophobization in a Dynamic Hydrogel for Creating Nonspecific Repeatable Underwater Adhesion
    (Weinheim : Wiley-VCH Verlag, 2020) Han, L.; Wang, M.; Prieto-López, L.O.; Deng, X.; Cui, J.
    Adhesive hydrogels are widely applied for biological and medical purposes; however, they are generally unable to adhere to tissues under wet/underwater conditions. Herein, described is a class of novel dynamic hydrogels that shows repeatable and long-term stable underwater adhesion to various substrates including wet biological tissues. The hydrogels have Fe3+-induced hydrophobic surfaces, which are dynamic and can undergo a self-hydrophobization process to achieve strong underwater adhesion to a diverse range of dried/wet substrates without the need for additional processes or reagents. It is also demonstrated that the hydrogels can directly adhere to biological tissues in the presence of under sweat, blood, or body fluid exposure, and that the adhesion is compatible with in vivo dynamic movements. This study provides a novel strategy for fabricating underwater adhesive hydrogels for many applications, such as soft robots, wearable devices, tissue adhesives, and wound dressings.
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    Double-Hydrophobic-Coating through Quenching for Hydrogels with Strong Resistance to Both Drying and Swelling
    (Chichester : John Wiley and Sons Ltd, 2020) Mredha, M.T.I.; Le, H.H.; Cui, J.; Jeon, I.
    In recent years, various hydrogels with a wide range of functionalities have been developed. However, owing to the two major drawbacks of hydrogels—air-drying and water-swelling—hydrogels developed thus far have yet to achieve most of their potential applications. Herein, a bioinspired, facile, and versatile method for fabricating hydrogels with high stability in both air and water is reported. This method includes the creation of a bioinspired homogeneous fusion layer of a hydrophobic polymer and oil in the outermost surface layer of the hydrogel via a double-hydrophobic-coating produced through quenching. As a proof-of-concept, this method is applied to a polyacrylamide hydrogel without compromising its mechanical properties. The coated hydrogel exhibits strong resistance to both drying in air and swelling in multiple aqueous environments. Furthermore, the versatility of this method is demonstrated using different types of hydrogels and oils. Because this method is easy to apply and is not dependent on hydrogel surface chemistry, it can significantly broaden the scope of next-generation hydrogels for real-world applications in both wet and dry environments.
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    Modeling the contact mechanics of hydrogels
    (Basel : MDPI, 2019) Mueser, M.H.; Li, H.; Bennewitz, R.
    A computationally lean model for the coarse-grained description of contact mechanics of hydrogels is proposed and characterized. It consists of a simple bead-spring model for the interaction within a chain, potentials describing the interaction between monomers and mold or confining walls, and a coarse-grained potential reflecting the solvent-mediated effective repulsion between non-bonded monomers. Moreover, crosslinking only takes place after the polymers have equilibrated in their mold. As such, the model is able to reflect the density, solvent quality, and the mold hydrophobicity that existed during the crosslinking of the polymers. Finally, such produced hydrogels are exposed to sinusoidal indenters. The simulations reveal a wavevector-dependent effective modulus E*(q) with the following properties: (i) stiffening under mechanical pressure, and a sensitivity of E*(q) on (ii) the degree of crosslinking at large wavelengths, (iii) the solvent quality, and (iv) the hydrophobicity of the mold in which the polymers were crosslinked. Finally, the simulations provide evidence that the elastic heterogeneity inherent to hydrogels can suffice to pin a compressed hydrogel to a microscopically frictionless wall that is undulated at a mesoscopic length scale. Although the model and simulations of this feasibility study are only two-dimensional, its generalization to three dimensions can be achieved in a straightforward fashion. © 2019 by the authors.
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    Polyester textile functionalization through incorporation of pH/thermo-responsive microgels. Part II: Polyester functionalization and characterization
    (Heidelberg : Springer, 2012) Glampedaki, P.; Calvimontes, A.; Dutschk, V.; Warmoeskerken, M.M.C.G.
    A new approach to functionalize the surface of polyester textiles is described in this study. Functionalization was achieved by incorporating pH/temperature-responsive polyelectrolyte microgels into the textile surface layer using UV irradiation. The aim of functionalization was to regulate polyester wettability according to ambient conditions by imparting stimuli-responsiveness from the microgel to the textile itself. Microgels consisted of pH/thermo-responsive microparticles of poly(N-isopropylacrylamide- co-acrylic acid) either alone or complexed with the pH-responsive natural polysaccharide chitosan. Scanning Electron Microscopy, X-ray Photoelectron Spectroscopy, ζ-potential measurements, and topographical analysis were used for surface characterization. Wettability of polyester textiles was assessed by dynamic wetting, water vapor transfer, and moisture regain measurements. One of the main findings showed that the polyester surface was rendered pH-responsive, both in acidic and alkaline pH region, owing to the microgel incorporation. With a marked relaxation in their structure and an increase in their microporosity, the functionalized textiles exhibited higher water vapor transfer rates both at 20 and 40 °C, and 65% relative humidity compared with the reference polyester. Also, at 40 °C, i.e., above the microgel Lower Critical Solution Temperature, the functionalized polyester textiles had lower moisture regains than the reference. Finally, the type of the incorporated microgel affected significantly the polyester total absorption times, with an up to 300% increase in one case and an up to 80% decrease in another case. These findings are promising for the development of functional textile materials with possible applications in biotechnology, technical, and protective clothing.
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    Hydrogel-based actuators: Possibilities and limitations
    (Amsterdam [u.a.] : Elsevier, 2014) Ionov, L.
    The rapid development of microtechnology in recent times has increased the necessity for the development of devices, which are able to perform mechanical work on the micro- and macroscale. Among all kinds of actuators, the ones based on stimuli-responsive hydrogels, which are three-dimensional polymer networks strongly imbibed with water, deserve particular attention. This paper aims to provide a brief overview of stimuli-responsive hydrogel actuators with respect to their sensitivity to different stimuli, different kinds of deformation, the possibilities of generating different types of movement, as well as their applications.
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    Macroporous smart hydrogels for fast-responsive piezoresistive chemical microsensors
    (Amsterdam [u.a.] : Elsevier, 2011) Schulz, V.; Zschoche, S.; Zhang, H.P.; Voit, B.; Gerlach, G.
    Within this work we present the synthesis and characterization of a pH-sensitive macroporous p(AAm-co-AA) hydrogel with an interconnected channel structure to enhance diffusion of aqueous solutions. The hydrogel is characterized by SEM and mercury porosimetry. Furthermore, the hydrogel is successfully integrated into piezoresistive microsensors measuring the hydrogel swelling due to pH changes. A response time reduction of about 80% compared to sensors with conventional non-porous hydrogels is accomplished.