Guido Saracco

Carbon capture is amongst the key emerging technologies for the mitigation of greenhouse gases (GHG) pollution. Several materials as adsorbents for CO₂ and other gases are being developed, which often involve using complex and expensive fabrication techniques. In this work, we suggest a sound, easy and cheap route for the production of nitrogen-doped carbon materials for CO₂ capture by pyrolysis of electrospun poly(acrylonitrile) (PAN) fibers. PAN fibers are generally processed following specific heat treatments involving up to three steps (to get complete graphitization), one of these being stabilization, during which PAN fibers are oxidized and stretched in the 200–300 °C temperature range. The effect of stabilization temperature on the chemical structure of the carbon nanofibers is investigated herein to ascertain the possible implication of incomplete conversion/condensation of nitrile groups to form pyridine moieties on the CO₂ adsorption capacity. The materials were tested in the pure CO₂ atmosphere at 20 °C achieving 18.3% of maximum weight increase (equivalent to an uptake of 4.16 mmol g⁻¹), proving the effectiveness of a high stabilization temperature as route for the improvement of CO₂ uptake.

In plant grana thylakoid membranes Photosystem II (PSII) associates with a variable number of antenna proteins (LHCII) to form different types of supercomplexes (PSII-LHCII), whose organization is dynamically adjusted in response to light cues, with the C₂S₂ more abundant in high-light and the C₂S₂M₂ in low-light. Paired PSII-LHCII supercomplexes interacting at their stromal surface from adjacent thylakoid membranes were previously suggested to mediate grana stacking. Here, we present the cryo-electron microscopy maps of paired C₂S₂ and C₂S₂M₂ supercomplexes isolated from pea plants grown in high-light and low-light, respectively. These maps show a different rotational offset between the two supercomplexes in the pair, responsible for modifying their reciprocal interaction and energetic connectivity. This evidence reveals a different way by which paired PSII-LHCII supercomplexes can mediate grana stacking at diverse irradiances. Electrostatic stromal interactions between LHCII trimers almost completely overlapping in the paired C₂S₂ can be the main determinant by which PSII-LHCII supercomplexes mediate grana stacking in plants grown in high-light, whereas the mutual interaction of stromal N-terminal loops of two facing Lhcb4 subunits in the paired C₂S₂M₂ can fulfil this task in plants grown in low-light. The high-light induced accumulation of the Lhcb4.3 protein in PSII-LHCII supercomplexes has been previously reported. Our cryo-electron microscopy map at 3.8 Å resolution of the C₂S₂ supercomplex isolated from plants grown in high-light suggests the presence of the Lhcb4.3 protein revealing peculiar structural features of this high-light-specific antenna important for photoprotection.

Hydrated salt thermochemical energy storage (TES) is a promising technology for high density energy storage, in principle opening the way for applications in seasonal storage. However, severe limitations are affecting large scale applications, related to their poor thermal and mechanical stability on hydration/dehydration cycling. In this paper, we report the preparation and characterization of composite materials manufactured with a wet impregnation method using strontium bromide hexahydrate (SBH) as a thermochemical storage material, combined with expanded natural graphite (G). In addition to these fully inorganic formulations, an organic polyelectrolyte (PDAC, polydiallyldimethylammonium chloride) was exploited in the structure, with the aim to stabilize the salt, while contributing to the sorption/desorption process. Different formulations were prepared with varying PDAC concentration to study its contribution to material morphology, by electron microscopy and X-ray diffraction, as well as water sorption/desorption properties, by thermogravimetry and differential calorimetry. Furthermore, the SBH/G/PDAC powder mixture was pressed to form tabs that were analyzed in a climatic chamber, which is evidence for an active role of PDAC in the improvement of water sorption, coupled with a significant enhancement of mechanical resistance upon hydration/dehydration cycling. Therefore, the addition of the polyelectrolyte is proposed as an innovative approach in the fabrication of efficient and durable TES devices.

The potential safety hazard associated to commonly used flame retardant chemicals generates a strong demand for new, sustainable, and high performing solutions to reduce the fire threats of widespread polymer foams. In this work, the production of self‐extinguishing, nonignitable, and flame resistant flexible polyurethane foams by means of simple layer‐by‐layer assembly of graphene oxide nanoplatelets is reported. The process builds a protective exoskeleton that completely wraps the complex 3D structure of the foam and is capable of stopping flame spread in flammability tests and preventing ignition when exposed to heat fluxes typical of developing fires. In addition, treated foams are found able to withstand the penetration of a flame torch, successfully protecting the unexposed side from thermal decomposition for more than 6 min. The outstanding temperature gradient greater than 500 °C cm⁻¹ achieved through the foam thickness makes the performances of these foams comparable to those of a silica aerogel, while maintaining excellent flexibility and toughness. The results reported in this paper represent a tremendous opportunity for the production of a novel class of organic and flexible foams, capable of ensuring unprecedented fire safety properties while relying on an easy, green, and straightforward approach to material design.

This research developed a comprehensive computer model for a lab-scale Slurry Bubble Column Reactor (SBCR) (0.1 m D_t and 2.5 m height) for Fischer–Tropsch (FT) synthesis under flexible operation of synthesis gas load flow rates. The variable loads of synthesis gas are set at 3.5, 5, 7.5 m³/h based on laboratory adjustments at three different operating temperatures (483, 493 and 503 K). A set of Partial Differential Equations (PDEs) in the form of mass transfer and chemical reaction are successfully coupled to predict the behavior of all the FT components in two phases (gas and liquid) over the reactor bed. In the gas phase, a single-bubble-class-diameter (SBCD) is adopted and the reduction of superficial gas velocity through the reactor length is incorporated into the model by the overall mass balance. Anderson Schulz Flory distribution is employed for reaction kinetics. The modeling results are in good agreement with experimental data. The results of dynamic modeling show that the steady state condition is attained within 10 min from start-up. Furthermore, they show that step-wise syngas flow rate does not have a detrimental influence on FT product selectivity and the dynamic modeling of the slurry reactor responds quite well to the load change conditions.

Consumers demand for portable audio/video/ICT devices has driven the development of advanced power technologies in recent years. Fuel cells are a clean technology with low emissions levels, able to work with renewable fuels and capable, in a next future, to replace conventional power systems meeting the targets of the Kyoto Protocol for a society based on sustainable energy systems. Within such a perspective, the objective of the European project MOREPOWER (Compact direct methanol fuel cells for portable applications) is to develop a low cost, low temperature, portable Direct Methanol Fuel Cell (DMFC; nominal power 250 W) of compact construction and modular design for the potential market area of weather stations, medical devices, signal units, gas sensors and security cameras. This investigation is focused on a conceptual study of the DMFC system carried out in the Matlab/Simulink platform. Two different DMFC configurations were devised in which alternative components arrangements along the methanol recycle line are considered. Based on a number of simulations, the system configuration characterized by a gas-liquid separator for carbon dioxide removal placed upstream the radiator for heat removal shows the most promising results, thanks to an easier design and operability of the radiator itself.