Recent studies have suggested that addition of electrically conductive biochar particles is an effective strategy to improve the methanogenic conversion of waste organic substrates, by promoting syntrophic associations between acetogenic and methanogenic organisms based on interspecies electron transfer processes. However, the underlying fundamentals of the process are still largely speculative and, therefore, a priori identification, screening, and even design of suitable biochar materials for a given biotechnological process are not yet possible. Here, three charcoal-like products (i.e., biochars) obtained from the pyrolysis of different lignocellulosic materials, (i.e., wheat bran pellets, coppiced woodlands, and orchard pruning) were tested for their capacity to enhance methane production from a food waste fermentate. In all biochar-supplemented (25 g/L) batch experiments, the complete methanogenic conversion of fermentate volatile fatty acids proceeded at a rate that was up to 5 times higher than that observed in the unamended (or sand-supplemented) controls. Fluorescent in situ hybridization analysis coupled with confocal laser scanning microscopy revealed an intimate association between archaea and bacteria around the biochar particles and provided a clear indication that biochar also shaped the composition of the microbial consortium. Based on the application of a suite of physico-chemical and electrochemical characterization techniques, we demonstrated that the positive effect of biochar is directly related to the electron-donating capacity (EDC) of the material, but is independent of its bulk electrical conductivity and specific surface area. The latter properties were all previously hypothesized to play a major role in the biochar-mediated interspecies electron transfer process in methanogenic consortia. Collectively, these results of this study suggest that for biochar addition in anaerobic digester operation, the screening and identification of the most suitable biochar material should be based on EDC determination, via simple electrochemical tests.

In this investigation, the crystal chemical characterization of one sample of woolly erionite-K (Lander County, NV, USA) was examined after suspension in a FeCl₂ solution, in anaerobic conditions. The aim of this study was to determine the effect of the chemical composition of erionite on its efficiency to bind iron. Inductively coupled plasma (ICP) results showed that the sample bound Fe(II) through an ion-exchange mechanism mainly involving Ca. In addition, chemical and structural data indicated that Fe(II) is fixed at the Ca3 site, six-fold coordinated to water molecules. According to Brunauer–Emmett–Teller (BET) sample surface area the amount of Fe(II) bound by the fibers was comparable with that retrieved for fibrous erionite-Na sample from Rome (OR, USA) for which the ion-exchange process mainly affected Na. This finding provides clear evidence of a strong tendency of Fe(II) to bind to the erionite structure. Furthermore, considering that the woolly erionite-K from Langer County differs markedly from erionite-Na from Rome in the extra-framework cation content, our observations indicate that the Fe binding efficiency is not significantly modulated by the chemical composition. Notably, Fe ion-exchanged and/or accumulated on the fiber surface can generate hydroxyl radicals via the Fenton reaction, thus influencing the potential carcinogenicity of the different erionite species.

δ-Al₂O₃ supported La, Mn, Co and Fe containing catalysts were prepared by impregnation of δ-Al₂O₃ with citrate-type precursors and calcination at 1073 K. The catalysts were characterized by X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (DRS), X-ray absorption spectroscopy (XAS), and BET specific surface area determination. XRD revealed the presence of δ-Al₂O₃ in all cases and, at 30 wt.% of metal loading, of other single (α-Mn₂O₃ and α-Fe₂O₃) or mixed (LaAlO₃, LaMnO₃, CoAl₂O₄ and LaFeO₃) oxide phases. XAS suggested the formation of some oxide phases also at lower loading. In particular, all Mn and 10 wt.% La–Mn containing samples revealed the formation of α-Mn₂O₃, while the 30 wt.% La–Mn bimetallic sample showed the formation of LaMnO₃ perovskite. All Co containing samples revealed the presence of CoAl₂O₄ spinel. Fe containing samples showed the formation of α-Fe₂O₃, while La–Fe containing ones, that of LaFeO₃ perovskite. Catalytic tests of CO oxidation were performed in the temperature range 300–800 K. The sample containing 30 wt.% of La and Mn in the form of LaMnO₃ perovskite dispersed on δ-Al₂O₃ was found the most active among all the examined catalysts. Most of the Co containing catalysts were found active at RT too, but they deactivated rapidly. None of the Fe-based samples was active at RT and these catalysts were found, on average, to be substantially less active than the Mn- and Co-based ones.

PFASs are a variety of ecologically persistent compounds of anthropogenic origin loosely included in many industrial products. In these, the carbon chain can be fully (perfluoroalkyl substances) or partially (polyfluoroalkyl substances) fluorinated. Their ubiquitous presence in many environmental compartments over the years and their long-lasting nature have given rise to concerns about the possible adverse effects of PFASs on ecosystems and human health. Among a number of remediation technologies, adsorption has been demonstrated to be a manageable and cost-effective method for the removal of PFASs in aqueous media. This study tested two novel and eco-friendly adsorbents (pinewood and date seeds biochar) on six different PFASs (PFOS, GenX, PFHxA, PFOA, PFDA, and PFTeDA). Batch sorption tests (24 h) were carried out to evaluate the removal efficiency of each PFAS substance in relation to the two biochars. All samples of liquid phase were analyzed by a developed and then a well-established method: (i) pre-treatment (centrifugation and filtration) and (ii) determination by high-performance liquid chromatography coupled with mass spectrometry (HPLC-MS/MS). The results evidenced a comparable adsorption capacity in both materials but greater in the long-chain PFASs. Such findings may lead to a promising path towards the use of waste-origin materials in the PFAS remediation field.

Groundwater is an extremely important resource that may, however, contain a variety of toxic and bioaccumulative contaminants. Traditional “Pump and Treat” technologies for treating contaminated groundwater are no longer time- or cost-effective; therefore, new technologies are needed. In this work, we synthesized core–shell materials of micrometric dimensions based on the interaction of iron particles (the core) and fermentable biopolymers such as polyhydroxybutyrate (PHB, the surrounding shell) to be used in permeable reactive barriers for the removal of chlorinated pollutants from contaminated groundwater. The materials were prepared by precipitation techniques that allowed stable preparations to be obtained, whose chemico-physical properties were thoroughly characterized by scanning electron microscopy, porosimetry, Fourier transform infrared spectroscopy (FTIR), thermogravimetric analyses, disc centrifuge analysis, and dynamic light scattering. The properties of the prepared materials are very promising, and may enhance the performance of permeable reactive barriers towards chlorinated compounds.

In this work, the consolidation efficiency of SiO₂ nanoparticles (synthesized in the Chemistry laboratories at the Tor Vergata University of Roma) was tested on Pietraforte sandstone surfaces belonging to the bell tower of San Lorenzo (Florence, Italy) and was fully investigated. Nanoparticles (synthesized in large-scale mass production) have been characterized by XRD—X-Ray Diffraction; Raman and FTIR—Fourier Transform Infrared spectroscopy; SEM—Scanning Electron Microscopy; while the Pietraforte sandstone morphology was examined by Porosimetry, capillary absorption test, surface hardness test, drilling resistance and tensile strength. The colorimetric measurements were also performed to characterize the optical modification exhibited by Pietraforte sandstones, especially after the SiO₂ treatments. Our results show that applying to the Pietraforte, the new consolidating agent based on SiO₂ nanoparticles, has several advantages, as they are more resistant to perforation, wear, and abrasion even long range (for long times of exposure and consolidating exercise against Florentine sandstone), compared to the CaCO₃ nanoparticles (tested in our previous paper), which instead show excellent performance but only close to their first application. This means that over time, their resistance to drilling decreases, they wear much more easily (compared to SiO₂-treated sandstone), and tend to exhibit quite a significant surface abrasion phenomena. The experimental results highlight that the SiO₂ consolidation efficiency on this kind of Florentine Pietraforte sandstone (having low porosity and a specific calcitic texture) seems to be higher in terms of water penetration protection, superficial cohesion forces, and an increase in surface resistance. Comparing the performance of SiO₂ nanoparticles with commercial consolidants in solvents such as Estel 1000 (tested here), we demonstrate that: (A) the restorative effects are obtained with a consolidation time over one week, significantly shorter when compared to the times of Estel 1000, exceeding 21 days; (B) SiO₂ nanoparticles perform better than Estel 1000 in terms of cohesion forces, also ensuring excellent preservation of the optical and color properties of the parent rock (without altering it after application).