Dr. María D. Alba

The use of zirconium in chemical industries generates a potential risk of Zr contamination in the environment, with particular concern for the decommissioning of uranium-graphite reactors. Among the natural adsorbents employed for the treatment of nuclear waste, clay minerals showed a very high affinity adsorption for radionuclides, but the influence of the chemical composition, pressure, temperature and time reaction have not yet been analysed on deep. Thus, the objective of this research is to explore several experimental conditions for an actual prediction of the behaviour of zirconium immobilization by clay minerals. The results have shown that factors such as zirconium cation nature (Zr4+ or ZrO2+), temperature, time and pH influence the extent of zirconium immobilization by clay minerals and the zirconium phases generated. At moderate conditions, zirconium tectosilicates are formed and evolve to zircon at high temperature and a longer time reaction.

Plant biomass is an attractive precursor to prepare activated carbons with high surface area for CO2 adsorption due to its low-cost and easy regeneration. Despite this interest, there are still remaining questions regarding the optimal processing conditions and the choice of activating agent. Moreover, since plant biomass shows a highly variable proportion of different biopolymers (cellulose, hemicellulose, lignin), it is important to understand the activation effect on each constituent. In this work, carbons obtained from pyrolysis of cellulose were activated using two potassium salts, using two different activation temperatures. The samples were characterized to elucidate the influence of the activation conditions on their CO2 adsorption capacity. In general, all the carbons activated at higher temperature showed higher adsorption capacity. These results are comparable with other carbons derived from biomass described in the bibliography. Among the activated carbons studied, the carbon activated only with KOH exhibits the highest CO2 adsorption capacity at 1 bar meanwhile the highest adsorption capacity at saturation pressure belongs to the carbon activated with larger ratio of KNO3.

Clay minerals are ceramics materials that are involved in a wide range of economic uses. But, their structure and composition are modified by heating and, consequently, compromise their final applications. The actual temperatures at which changes occur vary greatly from one group to another group and even for different specimens within a given group. The aim of this research has been to evaluate the thermal behaviour of a set of design swelling micas, Na-Mica-n (Mn) and compare them with a set of natural smectites. All samples were heated in the range 200 ^∘C to 1000 ^∘C; afterwards, they were rehydrated thorough water suspension (0.4% wt). The results have shown that swelling micas have better property of hydration/dehydration than natural clay minerals and those with higher layer charge exhibited higher rehydration ability and dehydration temperature.

Heavy metal contamination is a critical environmental issue, often involving complex multicomponent systems. Swelling brittle micas, a family of designer sorbents, have demonstrated exceptional heavy metal removal capabilities, yet their behabior in competitive adsorption systems remains largely unexplored. This study systematically investigates the simultaneous uptake of Pb^2+, Cd^2+, and Hg^2+ on both as-synthesized brittle mica and its thiol-functionalized counterpart. Using X-ray diffraction (XRD) and nuclear magnetic resonance (NMR), we reveal critical structural transformations occurring at both short- and long-range scales during adsorption. Our findings demonstrate that competitive adsorption governs metal uptake, leading to a reduction in total adsorption capacity compared to single-metal systems. However, selectivity toward specific metal cations remains unchanged, irrespective of competing species or surface functionalization. Overall, this study not only improves our understanding of heavy metal adsorption but also paves the way for more effective and sustainable sorbent design in environmental remediation.

The development of effective and environmentally friendly methods for separating hazardous radionuclides from waste poses a significant technological challenge. 137Cs and 131I are among the most important radionuclides discharged into the environment by nuclear power plants. One of the best ways to eliminate them involves adsorption on clay minerals. In this regard, studies have demonstrated that organofunctionalized clay minerals are effective adsorbents. Thus, this study investigates the capability of organofunctionalized synthetic design clay minerals to jointly eliminate cesium and iodine. The adsorbents studied are a range of organofunctionalized clay minerals with alkylammonium cations of different alkyl chain lengths (2, 3 and 18) and some physical mixtures of raw clay minerals and octadecylammonium compounds. Organofunctionalized synthetic swelling highly charged micas are effective adsorbents for the simultaneous adsorption of cesium and iodine. In addition, the optimal system is a mixture of Na-M4 with octadecylammonium (50% w/w).