Antibiotic contamination and the spread of antimicrobial resistant bacteria are global environmental issues. Given the growing consumption of antibiotics, it is crucial to reduce their presence in the environment. Adsorption is one of the most efficient methods for removing contaminants from water and wastewater. For this process to be effective, it is of key importance to identify adsorption mechanisms that allow an efficient and selective adsorbent to be chosen.Carbon-based materials (including activated carbon, biochar and black carbon) are typically used for the adsorptive removal of antibiotics. To enhance the efficiency of adsorption of pharmaceuticals, engineered biochars (physically, chemically and biologically modified biochar) and their composites have attracted increasing interests. Biochar-based sorbents can be produced from various feedstocks, including waste products. The use of "green", low cost or sustainable biochar for contaminant sorption yields economic and environmental benefits.Moreover, this is in line with global trends in creating a circular economy and sustainable development. This paper collates the most recent data on the consumption of antibiotics, their related environmental contamination, and their removal using biochar-based materials. Special attention is paid to the newly emerging approaches of biochar modification and biochar composites in relation to the antibiotic removal from water.

The present study focuses on the mechanism of swelling and evaluates interactions between solvents of different chemical characters (polar-ethanol, nonpolarn-heptane) and commercially available porous Amberlite polymers (XAD4, XAD16, XAD7HP) by temperatureprogrammed desorption (TPD). The first two polymers are the product of copolymerization of styrene and divinylbenzene. Despite having the same chemical composition, they differ in pore size and volume. The Amberlite XAD7HP is composed of an acrylic matrix and has lower pore volume and specific surface area than XAD16 and XAD4. All three resins have the ability to swell, though the per cent of polymeric network expansion during this process varies depending on the solvent used (e.g. in tetraethyl orthosilicate, XAD4 and XAD16 spherical particles increase in volume by 20-30%, while XAD7HP particles can expand by more than 120%). The TPD experiment was performed in dynamic linear and quasistatic heating mode. Based on thermogravimetric data, the desorption energy of selected liquids and pore size distribution in the swollen state were estimated. The obtained results are discussed in terms of both mathematical modelling and low-temperature nitrogen adsorption-desorption experiment.

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