RESUMEN
Lithium-oxygen batteries, with their very high energy density (3500 Wh kg-1), could represent a real breakthrough in the envisioned strategies towards more efficient energy storage solutions for a less and less carbonated energy mix. However, the problems associated with this technology are numerous. A first one is linked to the high reactivity of the lithium metal anode, while a second one is linked to the highly oxidative environment created by the cell's O2 saturation. Keeping in mind the necessity for greener materials in future energy storage solutions, in this work an innovative lithium protective membrane is prepared based on chitosan, a polysaccharide obtained from the deacetylation reaction of chitin. Chitosan was methacrylated through a simple, one-step reaction in water and then cross-linked by UV-induced radical polymerization. The obtained membranes were successively activated in liquid electrolyte and used as a lithium protection layer. The cells prepared with protected lithium were able to reach a higher full discharge capacity, and the chitosan's ability to slow down degradation processes was verified by post-mortem analyses. Moreover, in long cycling conditions, the protected lithium cell performed more than 40 cycles at 0.1 mA cm-2, at a fixed capacity of 0.5 mAh cm-2, retaining 100% coulombic efficiency, which is more than twice the lifespan of the bare lithium cell.
RESUMEN
Every year millions of people worldwide undergo surgical interventions, with the occurrence of mild or severe post-treatment consequences meaning that rehabilitation plays a key role in modern medicine. Considering the cases of burns and plastic surgery, the pressing need for new materials that can be used for wound patches or body fillers and are able to sustain tissue regeneration and promote cell adhesion and proliferation is clear. The challenges facing next-generation implant materials also include the need for improved structural properties for cellular organization and morphogenic guidance together with optimal mechanical, rheological, and topographical behavior. Herein, we propose for the first time a sodium alginate hydrogel obtained by a thiol-yne reaction, easily synthesized using carbodiimide chemistry in a two-step reaction. The hydrogels were formed in all cases within a few minutes of light irradiation, showing good self-standing properties under solicitation. The mechanical, rheological, topographical, and swelling properties of the gels were also tested and reported. Lastly, no cytotoxicity was detected among the hydrogels. Soluble extracts in culture media allowed cell proliferation, and no differences between samples were detected in terms of metabolic activity and DNA content. These results suggest the potential use of these cytocompatible hydrogels in tissue engineering and regenerative medicine.
RESUMEN
In this study, new photocurable biobased hydrogels deriving from chitosan and gelatin are designed and tested as sorbents for As(V) and Pb(II) removal from water. Those renewable materials were modified by a simple methacrylation reaction in order to make them light processable. The success of the reaction was evaluated by both 1H-NMR and FTIR spectroscopy. The reactivity of those formulations was subsequently investigated by a real-time photorheology test. The obtained hydrogels showed high swelling capability reaching up to 1200% in the case of methacrylated gelatin (GelMA). Subsequently, the Z-potential of the methacrylated chitosan (MCH) and GelMA was measured to correlate their electrostatic surface characteristics with their adsorption properties for As(V) and Pb(II). The pH of the solutions proved to have a huge influence on the As(V) and Pb(II) adsorption capacity of the obtained hydrogels. Furthermore, the effect of As(V) and Pb(II) initial concentration and contact time on the adsorption capability of MCH and GelMA were investigated and discussed. The MCH and GelMA hydrogels demonstrated to be promising sorbents for the removal of heavy metals from polluted waters.