Mechanical reinforcement of granular hydrogels.

Granular hydrogels are composed of hydrogel-based microparticles, so-called microgels, that are densely packed to form an ink that can be 3D printed, injected or cast into macroscopic structures. They are frequently used as tissue engineering scaffolds because microgels can be made biocompatible and the porosity of the granular hydrogels enables a fast exchange of reagents, waste products, and if properly designed even the infiltration of cells. Most of these granular hydrogels can be shaped into appropriate macroscopic structures, yet, these structures are mechanically rather weak. The poor mechanical properties prevent the use of these structures as load-bearing materials and hence, limit their field of applications. The mechanical properties of granular hydrogels depend on the composition of microgels and the interparticle interactions. In this review, we discuss different strategies to assemble microparticles into granular hydrogels and highlight the influence of inter-particle connections on the stiffness and toughness of the resulting materials. Mechanically strong and tough granular hydrogels have the potential to open up new fields of their use and thereby to contribute to fast advances in these fields. In particular, we envisage them to be well-suited as soft actuators and robots, tissue replacements, and adaptive sensors.

Recycling of Load-Bearing 3D Printable Double Network Granular Hydrogels.

Sustainable materials, such as recyclable polymers, become increasingly important as they are often environmentally friendlier than their one-time-use counterparts. In parallel, the trend toward more customized products demands for fast prototyping methods which allow processing materials into 3D objects that are often only used for a limited amount of time yet, that must be mechanically sufficiently robust to bear significant loads. Soft materials that satisfy the two rather contradictory needs remain to be shown. Here, the authors introduce a material that simultaneously fulfills both requirements, a 3D printable, recyclable double network granular hydrogel (rDNGH). This hydrogel is composed of poly(2-acrylamido-2-methylpropane sulfonic acid) microparticles that are covalently crosslinked through a disulfide-based percolating network. The possibility to independently degrade the percolating network, with no harm to the primary network contained within the microgels, renders the recovery of the microgels efficient. As a result, the recycled material pertains a stiffness and toughness that are similar to those of the pristine material. Importantly, this process can be extended to the fabrication of recyclable hard plastics made of, for example, dried rDNGHs. The authors envision this approach to serve as foundation for a paradigm shift in the design of new sustainable soft materials and plastics.

Shape retaining self-healing metal-coordinated hydrogels.

Metal-coordinated hydrogels are physical hydrogels entirely crosslinked by complexes between ligand decorated polymers and metal ions. The mechanical properties of these hydrogels strongly depend on the density and dynamics of metal-coordinated interactions. Most commonly, telechelic metal-coordinated hydrogels contain catechol or histidine ligands, although hydrogels containing a stronger complexation agent, nitrocatechol, have been reported. Here, we introduce a pyrogallol end-functionalized polymer that can be crosslinked with di- and trivalent ions, in contrast to previously reported metal-coordinated hydrogels. We can tune the mechanical properties of the hydrogels with the types of ions used and the density of crosslinking sites. Ions form nm-sized precipitates that bind to pyrogallols and impart distinct properties to the hydrogels: strong ion-pyrogallol interactions that form in the presence of Al3+, V3+, Mn2+, Fe3+, Co2+, Ni2+ and Cu2+ result in long relaxation times. The resulting hydrogels display solid-like yet reversible mechanical properties, such that they can be processed into macroscopic 3D structures that retain their shapes. Weak ion-pyrogallol interactions that form in the presence of Ca2+ or Zn2+ result in short relaxation times. The resulting hydrogels display a fast self-healing behavior, suited for underwater glues, for example. The flexibility of tuning the mechanical properties of hydrogels simply by selecting the adequate ion-pyrogallol pair broadens the mechanical properties of metal-coordinated hydrogels to suit a wide range of applications that require them to retain their shape for a given time to act as dampers.