Use of Foundry Sands in the Production of Ceramic and Geopolymers for Sustainable Construction Materials

The aim of this research was to evaluate the possibility of reusing waste foundry sands derived from the production of cast iron as a secondary raw material for the production of building materials obtained both by high-temperature (ceramic tiles and bricks) and room-temperature (binders such as geopolymers) consolidation. This approach can reduce the current demand for quarry sand and/or aluminosilicate precursors from the construction materials industries. Samples for porcelain stoneware and bricks were produced, replacing the standard sand contained in the mixtures with waste foundry sand in percentages of 10%, 50%, and 100% by weight. For geopolymers, the sand was used as a substitution for metakaolin (30, 50, 70 wt%) as an aluminosilicate precursor rather than as an aggregate to obtain geopolymer pastes. Ceramic samples obtained using waste foundry sand were characterized by tests for linear shrinkage, water absorption, and colorimetry. Geopolymers formulations, produced with a Si/Al ratio of 1.8 and Na/Al = 1, were characterized to evaluate their chemical stability through measurements of pH and ionic conductivity, integrity in water, compressive strength, and microstructural analysis. The results show that the addition of foundry sand up to 50% did not significantly affect the chemical-physical properties of the ceramic materials. However, for geopolymers, acceptable levels of chemical stability and mechanical strength were only achieved when using samples made with 30% foundry sand as a replacement for metakaolin

Gene-environment interaction analysis of redox-related metals and genetic variants with plasma metabolic patterns in a general population from Spain: The Hortega Study

Background: Limited studies have evaluated the joint influence of redox-related metals and genetic variation on metabolic pathways. We analyzed the association of 11 metals with metabolic patterns, and the interacting role of candidate genetic variants, in 1145 participants from the Hortega Study, a population-based sample from Spain. Methods: Urine antimony (Sb), arsenic, barium (Ba), cadmium (Cd), chromium (Cr), cobalt (Co), molybdenum (Mo) and vanadium (V), and plasma copper (Cu), selenium (Se) and zinc (Zn) were measured by ICP-MS and AAS, respectively. We summarized 54 plasma metabolites, measured with targeted NMR, by estimating metabolic principal components (mPC). Redox-related SNPs (N = 291) were measured by oligo-ligation assay. Results: In our study, the association with metabolic principal component (mPC) 1 (reflecting non-essential and essential amino acids, including branched chain, and bacterial co-metabolism versus fatty acids and VLDL subclasses) was positive for Se and Zn, but inverse for Cu, arsenobetaine-corrected arsenic (As) and Sb. The association with mPC2 (reflecting essential amino acids, including aromatic, and bacterial co-metabolism) was inverse for Se, Zn and Cd. The association with mPC3 (reflecting LDL subclasses) was positive for Cu, Se and Zn, but inverse for Co. The association for mPC4 (reflecting HDL subclasses) was positive for Sb, but inverse for plasma Zn. These associations were mainly driven by Cu and Sb for mPC1; Se, Zn and Cd for mPC2; Co, Se and Zn for mPC3; and Zn for mPC4. The most SNP-metal interacting genes were NOX1, GSR, GCLC, AGT and REN. Co and Zn showed the highest number of interactions with genetic variants associated to enriched endocrine, cardiovascular and neurological pathways. Conclusions: Exposures to Co, Cu, Se, Zn, As, Cd and Sb were associated with several metabolic patterns involved in chronic disease. Carriers of redox-related variants may have differential susceptibility to metabolic alterations associated to excessive exposure to metals.This work was supported by the Strategic Action for Research in Health sciences [CP12/03080, PI15/00071, PI10/0082, PI13/01848, PI14/00874, PI16/01402, PI21/00506 and PI11/00726], CIBER Fisio patología Obesidad y Nutrición (CIBEROBN) (CIBER-02-08-2009, CB06/03 and CB12/03/30,016), the State Agency for Research (PID2019-108973RB- C21 and C22), the Valencia Government (GRUPOS 03/101; PROMETEO/2009/029 and ACOMP/2013/039, IDI FEDER/2021/072 and GRISOLIAP/2021/119), the Castilla-Leon Government (GRS/279/A/08) and European Network of Excellence Ingenious Hypercare (EPSS-037093) from the European Commission. The Strategic Action for Research in Health sciences, CIBERDEM and CIBEROBN are initiatives from Carlos III Health Institute Madrid and cofunded with European Funds for Regional Development (FEDER). The State Agency for Research and Carlos III Health Institute belong to the Spanish Ministry of Science and Innovation. ADR received the support of a fellowship from “la Caixa” Foundation (ID 100010434) (fellowship code “LCF/BQ/DR19/11740016”). MGP received the support of a fellowship from “la Caixa” Foundation (ID 100010434, fellowship code LCFLCF/BQ/DI18/11660001). The funding bodies had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.S

New strategy for microplastic degradation: Green photocatalysis using a protein-based porous N-TiO2 semiconductor

Currently, the global community considers microplastics as a marine pollutant of emerging concern. To mitigate the oceanic microplastic pollution, it is necessary to reduce inputs from inland. In this sense, we present the first report on the use of photocatalysis for the degradation of HDPE microplastics extracted from a commercially available facial scrub. This was achieved by using two proposed semiconductors based on N-TiO2. One was green synthesized using the extrapallial fluid of fresh blue mussels, which presented an excellent capacity to promote photocatalytic degradation in solid and aqueous environments; while the second photocatalyst, obtained from a conventional sol-gel synthesis, presented good capacity to promote mass loss of the as-extracted microplastics in an aqueous environment. Mass losses, SEM and FTIR analysis confirmed HDPE degradation. Results showed that environmental conditions, microplastics/N-TiO2 interaction and the N-TiO2 surface area should be carefully set and monitored in order of avoiding the arrest of photocatalysisCurrently, the global community considers microplastics as a marine pollutant of emerging concern. To mitigate the oceanic microplastic pollution, it is necessary to reduce inputs from inland. In this sense, we present the first report on the use of photocatalysis for the degradation of HDPE microplastics extracted from a commercially available facial scrub. This was achieved by using two proposed semiconductors based on N-TiO2. One was green synthesized using the extrapallial fluid of fresh blue mussels, which presented an excellent capacity to promote photocatalytic degradation in solid and aqueous environments; while the second photocatalyst, obtained from a conventional sol-gel synthesis, presented good capacity to promote mass loss of the as-extracted microplastics in an aqueous environment. Mass losses, SEM and FTIR analysis confirmed HDPE degradation. Results showed that environmental conditions, microplastics/N-TiO2 interaction and the N-TiO2 surface area should be carefully set and monitored in order of avoiding the arrest of photocatalysis

Microplastic pollution reduction by a carbon and nitrogen-doped TiO2: Effect of pH and temperature in the photocatalytic degradation process

Microplastics (MPs) are pollutants formed by plastics 64 5 mm and are present in marine and terrestrial environments. Due to their large surface to volume ratio and chemical surface properties, MPs adsorb hazardous chemicals from their surrounding environment. When MPs are consumed by fauna, they transfer those substances through the trophic chain. An essential issue of MPs is their disposal. Due to their size, the disposal methods commonly used for plastic items are not suited for MPs. Here, photocatalysis in an aqueous medium is proposed as an alternative to fight MPs pollution. Although the photocatalysis of MPs has been reported, the effect of operating variables in the process has not been investigated. To fill this gap, the impact of pH and temperature on the degradation process of HDPE MPs was investigated using C,N-TiO2 and visible light. Degradation was followed by mass loss, carbonyl index calculation and microscopy. It was found that photocatalysis at low temperature (0 \ub0C) increases MPs\u2019 surface area by fragmentation, and low pH value (pH 3) favours hydroperoxide formation during photooxidation. By using the design of experiments tool, it was demonstrated that there is a combined effect of pH and temperature in the photocatalysis of HDP

The role of the reactive species involved in the photocatalytic degradation of hdpe microplastics using c,n-tio2 powders

Microplastics (MPs) are distributed in a wide range of aquatic and terrestrial ecosystems throughout the planet. They are known to adsorb hazardous substances and can transfer them across the trophic web. To eliminate MPs pollution in an environmentally friendly process, we propose using a photocatalytic process that can easily be implemented in wastewater treatment plants (WWTPs). As photocatalysis involves the formation of reactive species such as holes (h+), electrons (e−), hydroxyl (OH•), and superoxide ion (O2•−) radicals, it is imperative to determine the role of those species in the degradation process to design an effective photocatalytic system. However, for MPs, this information is limited in the literature. Therefore, we present such reactive species’ role in the degradation of high-density polyethylene (HDPE) MPs using C,N-TiO2. Tert-butanol, isopropyl alcohol (IPA), Tiron, and Cu(NO3)2 were confirmed as adequate OH•, h+, O2•− and e− scavengers. These results revealed for the first time that the formation of free OH• through the pathways involving the photogenerated e− plays an essential role in the MPs’ degradation. Furthermore, the degradation behaviors observed when h+ and O2•− were removed from the reaction system suggest that these species can also perform the initiating step of degradation

Biodiversidad en la cuenca del Orinoco. Bases científicas para la identificación de áreas prioritarias para la conservación y uso sostenible de la biodiversidad

Es un placer para el Instituto de Investigación de Recursos Biológicos Alexander von Humboldt presentar a la comunidad científica, conservacionista y autoridades ambientales de Colombia y Venezuela la obra Biodiversidad de la cuenca del Orinoco: bases científicas para la identificación de áreas prioritarias para la conservación y el uso sostenible de la biodiversidad. Este libro es fruto de un esfuerzo de una década de trabajo y recoge numerosos proyectos de carácter institucional que han venido desarrollándose en la Orinoquia, incluyendo el Plan de acción en biodiversidad para la cuenca del Orinoco (2005-2015), además de los resultados de reuniones técnicas de carácter binacional