The global impact of water and soil contamination has become a serious issue that affects the world and all living beings. In this sense, multiple treatment alternatives have been developed at different scales to improve quality. Among them, biochar has become a suitable alternative for environmental remediation due to its high efficiency and low cost, and the raw material used for its production comes from residual biomass. A biochar is a carbonaceous material with interesting physicochemical properties (e.g., high surface area, porosity, and functional surface groups), which can be prepared by different synthesis methods using agricultural wastes (branches of banana rachis, cocoa shells, cane bagasse, among others) as feedstock. This state-of-the-art review is based on a general description of biochar for environmental remediation. Biochar’s production, synthesis, and multiple uses have also been analyzed. In addition, this work shows some alternatives used to improve the biochar properties and thus its efficiency for several applications, like removing heavy metals, oil, dyes, and other toxic pollutants. Physical and chemical modifications, precursors, dopants, and promoting agents (e.g., Fe and N species) have been discussed. Finally, the primary uses of biochar and the corresponding mechanism to improve water and soil quality (via adsorption, heterogeneous photocatalysis, and advanced oxidation processes) have been described, both at laboratory and medium and large scales. Considering all the advantages, synthesis methods, and applications, biochar is a promising alternative with a high potential to mitigate environmental problems by improving water and soil quality, reducing greenhouse gas emissions, and promoting the circular economy through residual biomass, generating value-added products for several uses.

The development of bio-based materials has been a consequence of the environmental awareness generated over time. The versatility of native starch is a promising starting point for manufacturing environmentally friendly materials. This work aims to compile information on the advancements in research on thermoplastic starch (TPS) nanocomposites after the addition of mainly these four nanofillers: natural montmorillonite (MMT), organically modified montmorillonite (O-MMT), cellulose nanocrystals (CNC), and cellulose nanofibers (CNF). The analyzed properties of nanocomposites were mechanical, barrier, optical, and degradability. The most important results were that as the nanofiller increases, the TPS modulus and strength increase; however, the elongation decreases. Furthermore, the barrier properties indicate that that the incorporation of nanofillers confers superior hydrophobicity. However, the optical properties (transparency and luminosity) are mostly reduced, and the color variation is more evident with the addition of these fillers. The biodegradability rate increases with these nanocompounds, as demonstrated by the study of the method of burial in the soil. The results of this compilation show that the compatibility, proper dispersion, and distribution of nanofiller through the TPS matrix are critical factors in overcoming the limitations of starch when extending the applications of these biomaterials. TPS nanocomposites are materials with great potential for improvement. Exploring new sources of starch and natural nano-reinforcement could lead to a genuinely eco-friendly material that can replace traditional polymers in applications such as packaging.

Nowadays, companies and researchers are concerned about the negative consequences of using synthetic polymers and direct their efforts to create new alternatives such as biocomposites. This study investigated the effect of biobased SiO${}_2$ on the properties of poly(L-lactic acid)/SiO${}_2$ (PLLA/SiO${}_2$) and poly(L-lactic acid)/SiO${}_2$/poly(ethylene glycol) (PLLA/SiO${}_2$/PEG) composites. The SiO${}_2$ was obtained from rice husk incineration and mixed with PLLA at various concentrations (5, 10, and 15 wt.%) via melt extrusion before compression molding. Furthermore, PLLA/SiO${}_2$/PEG composites with various PEG concentrations (0, 3, 5, and 10 wt.%) with 10 wt.% SiO${}_2$ were produced. The sample morphology was studied by scanning electron microscopy (SEM) to analyze the dispersion/adhesion of SiO${}_2$ in the polymer matrix and differential scanning calorimetry (DSC) was used under isothermal and non-isothermal conditions to study the thermal properties of the samples, which was complemented by thermal stability study using thermogravimetric analysis (TGA). Rheological analysis was performed to investigate the viscoelastic behavior of the composites in the melt state. At the same time, tensile mechanical properties were obtained at room temperature to determine their properties in the solid state. DSC and X-ray diffraction analysis (XRD) were combined to determine the crystalline state of the samples. Finally, gas permeation measurements were performed using a variable pressure (constant volume) method to analyze the permeability of different gases (CO${}_2$, CH${}_4$, O${}_2$, and H${}_2$). The results showed that SiO${}_2$ decreased the PLLA chain mobility, slowing the crystallization process and lowering the gas permeability while increasing Young’s modulus, thermal stability, and viscosity. However, PEG addition increased the crystallization rate compared to the neat PLLA (+40%), and its elongation at break (+26%), leading to more flexible/ductile samples. Due to improved silica dispersion and PLLA chain mobility, the material’s viscosity and gas permeability (+50%) were also improved with PEG addition. This research uses material considered as waste to improve the properties of PLA, obtaining a material with the potential to be used for packaging.

In the Ecuadorian Amazonia, there is a concern about the presence of high concentrations of cadmium (Cd) in rivers and sediments because of changes in land use and anthropogenic activities, e.g., mining and oil exploitation. Hence, the research related to water treatment processes to meet environmental standards has gained relevance. The use of biochar (BC) as adsorbent is considered a promising and low-cost alternative to improve the water quality in developing countries. In this work, lignocellulosic wastes from Guadua angustifolia were transformed through thermochemical treatments, into a promising carbonaceous material, such as BC. BC samples were prepared by pyrolysis (termed pyrochar, PC) and hydrothermal carbonization (termed hydrochar, HC). Their physicochemical properties were correlated with the Cd adsorption removal performance, analyzing the effect of adsorbent dosage, initial solution pH, adsorption kinetics and adsorption isotherms. HC showed the highest Cd adsorption performance, due to the presence of a higher number of oxygenated functional groups, as confirmed by FTIR, XPS and Raman spectroscopy. This research has proposed a sustainable alternative for the recovery of an available waste, contributing to mitigate the effects of the presence of metals on the health and economy of the most vulnerable sectors of society.

In the first step to obtain an efficient nano-antenna in a bottom-up approach, new hybrid materials were synthesized using a set of layered double hydroxides (LDHs) with basic properties and pure chlorophyll a (Chl a). The stability of the adsorbed monolayer of Chl a was shown to be dependent on the nature and the ratio of the different metal ions present in the LDHs tested. The hybrid materials turned out to be adequate for stabilizing Chl a on Mg/Al LDHs for more than a month under ambient conditions while a limited catalytic decomposition was observed for the Ni/Al LDHs leading to the formation of pheophytin. These changes were followed by namely XRD, DR-UV-vis and fluorescence spectroscopies of the hybrid antennae and of the solutions obtained from their lixiviation with acetone or diethylether. On Mg/Al hydrotalcites the stability of the adsorbed Chl a was equivalent for values of the metal atom ratio ranging from 2 to 4. The latter hybrids should constitute a good basis to form efficient nanoscale light harvesting units following intercalation of selected dyes. This work describes an efficient preparation of Chl a that allows scale-up as well as the obtention of a stable Chl a monolayer on the surface of various LDHs.

The nuclear plant accident of Fukushima Daiichi occurred following a tsunami on March 11th 2011 and gave rise to the production of large volume aqueous outflows containing radioactive cesium and seawater. This problem urged researchers to develop materials suitable for high flux continuous sorption processes able to promote the selective entrapment of cesium while sodium is widely present in the contaminated outflows. This work is focused on the achievement of silica monoliths with hierarchical porosity (meso- and macropores) combining on one hand enhanced mechanical strength thanks to a calcination step and on the other hand a one-pot functionalisation procedure in order to insert metal hexacyanoferrate (MHCF) particles inside the pores. This combination is generally difficult to achieve due to the MHCF alteration for temperatures above 200 °C. However, these problems can be avoided following the procedure described in this paper. Finally synthetic routes for meso/macroporous silica monoliths functionalised with sorbent particles highly selective towards cesium, CoHCF, CuHCF and ZnHCF are described. The weight ratio of MHCF reaches 7.1% wt with a total cesium sorption capacity of 24.1 mg g⁻¹ in the case of monoliths functionalised with ZnHCF. This value is not altered by the presence of sodium in the aqueous solution. MHCF particles are located mainly inside the macropores while the mesopore network allows for a high exchange surface between the aqueous outflows and MHCF particles embedded in the monoliths.