A large amount of the globally produced plastics are not treated and are eventually released into landfills or natural environments, including surface waters. The plastics that enter the aquatic environment are very often microplastics, which are produced in households by the slow degradation or abrasion of plastic products, or as whole plastic products, which eventually degrade (abrasion, photodegradation). Together with microplastics, other pollutants such as pharmaceuticals of various kinds enter surface waters—both of these counterparts can interact with each other as well as with organic and inorganic molecules available in the natural environment. The aim of this study was to identify the interaction of microplastics with pharmaceuticals, especially under conditions that are common in inland waters as well as the seas and oceans that the rivers feed their water into. It was found that salinity has a great impact on the sorption capacity of microplastics and pharmaceuticals. The sorption of naturally occurring humic substances (humic and fulvic acids) can greatly increase when the microplastic–pharmaceutical complex is formed; however, the priority of the interaction happens with pharmaceuticals and humic substances. Such complexes can influence the organisms that feed on small organic-matter particles, as they can be mistaken for food and thus be transferred throughout the food chain.

In this study, new composite materials of montmorillonite, biochar, or aerosil, containing metal–organic frameworks (MOF) were synthesized in situ. Overall, three different MOFs—CuBTC, UTSA-16, and UiO-66-BTEC—were used. Obtained adsorbents were characterized using powder X-ray diffraction, thermogravimetric analysis, nitrogen adsorption porosimetry, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and Fourier transform infrared spectrophotometry. Additionally, the content of metallic and nonmetallic elements was determined to investigate the crystalline structure, surface morphology, thermal stability of the obtained MOF-composites, etc. Cyclic CO₂ adsorption analysis was performed using the thermogravimetric approach, modeling adsorption from flue gasses. In our study, the addition of aerosil to CuBTC (CuBTC-A-15) enhanced the sorbed CO₂ amount by 90.2% and the addition of biochar (CuBTC-BC-5) increased adsorbed the CO₂ amount by 75.5% in comparison to pristine CuBTC obtained in this study. Moreover, the addition of montmorillonite (CuBTC-Mt-15) increased the adsorbed amount of CO₂ by 27%. CuBTC-A-15 and CuBTC-BC-5 are considered to be the most perspective adsorbents, capturing 3.7 mmol/g CO₂ and showing good stability after 20 adsorption-desorption cycles.

Carbon capture is among the most sustainable strategies to limit carbon dioxide emissions, which account for a large share of human impact on climate change and ecosystem destruction. This growing threat calls for novel solutions to reduce emissions on an industrial level. Carbon capture by amorphous solids is among the most reasonable options as it requires less energy when compared to other techniques and has comparatively lower development and maintenance costs. In this respect, the method of carbon dioxide adsorption by solids can be used in the long-term and on an industrial scale. Furthermore, certain sorbents are reusable, which makes their use for carbon capture economically justified and acquisition of natural resources full and sustainable. Clay minerals, which are a universally available and versatile material, are amidst such sorbents. These materials are capable of interlayer and surface adsorption of carbon dioxide. In addition, their modification allows to improve carbon dioxide adsorption capabilities even more. The aim of the review is to discuss the prospective of the most widely available clay minerals in the Baltic States for large-scale carbon dioxide emission reduction and to suggest suitable approaches for clay modification to improve carbon dioxide adsorption capacity.