Control of the interlayer composition and morphology of LDH by proper choice of salt, nitrate or chloride and the amount of urea.

Plastic pollution and food waste are two global issues with much in common. Plastic containers were introduced as a practical and easy remedy to improve food preservation and reduce the risk of creating waste, but ironically, to address one problem, another has been made worse. The spread of single‐use containers has dramatically increased the amount of plastic that has to be discarded, and the most urgent task is now to find a solution to what has become part of the problem. An innovative way around it consists of promoting the valorization of food residues by turning them into novel materials for packaging. Although the results are promising, the aim of completely replacing plastics with biodegradable materials still seems far from being achieved. This review illustrates the main strategies adopted thus far to produce new bioplastic materials and composites from waste resources and focuses on the pros and cons of the food recovery process to look for the aspects that represent an obstacle to the development of the circular food economy on an industrial scale.

Surface-modified ZnAl layered double hydroxides (LDHs) were prepared by reaction of AgNO₃, with both ZnAlCl (LDH1) and ZnAlCO₃ exchanged on the surface with chloride anions (LDH3). In this way, AgCl nanoparticles with crystalline domains ranging from 40 to 100 nm were grown on the LDH surface. An additional sample was prepared by partial reduction of silver to obtain Ag@AgCl-LDH (LDH2). The composites were tested as catalysts in Rhodamine B (RhB) degradation, wherein LDH2 showed complete cleavage of RhB after 45 min of irradiation versus 70 min needed in the presence of AgCl. This time decreased to 35 min for LDH1 and 15 min for LDH3, underlining the role of the AgCl dimensions and anion in the interlayer region. Studies on the reactive species involved in the degradation process revealed that, for all catalysts, O₂·⁻ was the main active species, while, to some extent, holes contribute to the activity of the LDH3. Finally, the composites showed high bactericidal activity, under irradiation, against Escherichia coli, comparable with that of Gentamicin, the positive control. A synergic effect of silver released from the composites and the production of reactive oxygen species was considered.

The chloride form of MgAl layered double hydroxide (hereafter MgAlCl) as an anion exchanger and the semisodic form of α-zirconium phosphate (hereafter ZrPNaH) as a cation exchanger are proposed as new cleaning agents for the removal of gypsum from ancient monuments. The ability of these exchangers to capture the calcium and sulphate ions of the gypsum powder was first investigated separately and then as a coupled system. MgAlCl/gypsum, ZrPNaH/gypsum and MgAlCl/ZrPNaH/gypsum mixtures were characterized by X-ray powder diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and dispersive X-ray spectroscopy (EDX). ZrPNaH in the form of a wet paste exhibited a rapid uptake of calcium from gypsum powder via Na⁺ and H⁺/Ca²⁺ cation exchange. Gypsum powder was also successfully dissolved by a wet paste of MgAlCl by exploiting the Cl⁻/SO₄ ²⁻ anion exchange reaction. However, the dehydration of the paste favoured the reprecipitation of a secondary gypsum that was characterized by lower crystallinity and smaller particle size than the pristine gypsum. The combination of wet MgAlCl and ZrPNaH showed a synergic effect on the dissolution of gypsum and partially prevented the reprecipitation of gypsum in the dry paste. Finally, a preliminary test of the removal of gypsum crust grown on a sandstone sample was performed.