The CO2 capture using adsorption can reduce the carbon footprint, increasing the sustainability of the process without the production of wastes present in commonly used industrial operations. The present research work analyses the effect of the doping-agents incorporation in carbon materials upon adsorption and separation of gases, specifically for carbon dioxide and nitrogen. The carbons precursor was polyacrylonitrile (PAN), which enabled the incorporation of nitrogen atoms in the structure, whereas sulphur doping was reached using pure sulphur after the carbonisation step. The influence of several variables (such as temperature or pressure) and characteristics of synthesised materials (mainly corresponding to surface characteristics) on carbon dioxide separation has been evaluated. Adsorption isotherms were determined for each gas (CO2 and N2) at different temperatures and pressures. Different adsorption models were evaluated to fit the experimental data. In general, the Toth isotherm described better the adsorption for both gases. Important parameters such as CO2/N2 selectivity and heat of adsorption were determined using the IAS theory and the experimental isotherms at different temperatures, respectively. Non-activated carbons generated from PAN carbonisation without sulphur addition showed the highest values of selectivity (up to 400) and adsorption heat (up to 40 kJ mol−1), mainly at low pressures and at low carbon dioxide uptakes, respectively. Furthermore, thanks to their high adsorption capacity, these carbons can be applied for carbon dioxide separation from mixtures with nitrogen.

The main purpose of this work is to contribute to understanding the mechanism of oxidation of the polymeric components of common disposable masks used during the COVID-19 pandemic to offer the chemical basis to understand their long-term behavior under typical environmental conditions. Artificial aging of representative mask layers under isothermal conditions (110 °C) or accelerated photoaging showed that all the PP-made components underwent a fast oxidation process, following the typical hydrocarbon oxidation mechanism. In particular, yellowing and the melting temperature drop are early indicators of their diffusion-limited oxidation. Morphology changes also induced a loss of mechanical properties, observable as embrittlement of the fabric fibers. Results were validated through preliminary outdoor aging of masks, which allows us to predict they will suffer fast and extensive oxidation only in the case of contemporary exposure to sunlight and relatively high environmental temperature, leading to their extensive breakdown in the form of microfiber fragments, i.e., microplastics.

The main purpose of this work is to contribute to understanding the mechanism of oxidation of the polymeric components of common disposable masks used during the COVID-19 pandemic to offer the chemical basis to predict their long-term behaviour under typical environmental conditions. Artificial ageing of representative mask layers under isothermal conditions (110℃) or accelerated photoageing showed that all the PP-made components underwent a fast oxidation process, following the typical hydrocarbon oxidation mechanism. In particular, yellowing and the melting temperature drop are early indicators of their diffusion-limited oxidation. Morphology changes also induced a loss of mechanical properties, observable as embrittlement of the fabric fibres. Results were validated through preliminary outdoor ageing of masks, which allows us to predict they will suffer fast and extensive oxidation only in the case of contemporary exposure to sunlight and relatively high environmental temperature, leading to their extensive breakdown in the form of microfiber fragments, i.e., microplastics.