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The presence of pharmaceuticals or their active metabolites in receiving waters is a sign of the inefficient removal of bioactive substrates from wastewater. Adsorption seems to be the most effective and inexpensive method of their removal. Waste management aimed at sorbents is a promising way to sustain several sustainable development goals. In the presented paper, the removal of the two most widely used drugs in the wastewater was examined. Diclofenac and carbamazepine were removed from water and wastewater using textile waste-derived sorbents. Their removal efficiency was verified by testing several process parameters such as the time of the sorption, the presence of interfering inorganic ions, the presence of dissolved organic matter, the initial pH and ionic strength of the solution, and various water matrices. The adsorption capacity was noted for diclofenac (57.1 mg/g) and carbamazepine (21.25 mg/g). The tested process parameters (pH, presence of inorganic ions, dissolved organic matter, ionic strength, water matrix) confirmed that the presented waste materials possessed a great potential for pharmaceutical removal from water matrices. [ABSTRACT FROM AUTHOR]

Basalt fiber reinforced polypropylene composites with two initial fiber lengths (3.2 and 6.4 mm) were fabricated using twin‐screw extrusion compounding. In the case of composites with smaller initial fiber length, basalt fibers predominantly served as nucleating agents for polypropylene thereby resulting in an increase in the degree of crystallinity. The addition of polypropylene‐g‐maleic anhydride (PP‐g‐MA) caused the matrix to become amorphous, which was due to the establishment of a fiber–matrix interphase. This behavior was different for the composites with relatively larger initial fiber length especially at higher fiber content. The reduction in fiber length in the composites caused a decrease in crystallinity, as this hindered the ability of the polypropylene matrix to form crystals. Addition of PP‐g‐MA established a fiber–matrix interphase thereby synergistically contributing to the increased matrix amorphousness of the basalt fiber reinforced polypropylene composites with 6.4 mm initial fiber length. Reduced fiber length due to processing also accelerated the thermal degradation of the composites with an initial fiber length of 6.4 mm. However, the reduction in fiber length due to processing resulted in increased fiber orientation, which contributed to the improvement in tensile and flexural properties of the basalt fiber reinforced polypropylene composites with an initial fiber length of 6.4 mm. At 30% fiber content, the tensile strength and modulus of basalt fiber reinforced matrix modified polypropylene composites with 6.4 mm initial fiber length improved by 18% and 13% as compared with the composites with 3.2 mm initial fiber length. [ABSTRACT FROM AUTHOR]

A mixture of zeolite X and A, derived from coal fly ash (CFA), was protonated and utilized as an acid catalyst to decompose single‐use plastics (SUP) waste into lighter hydrocarbons. Low‐density polyethylene (LDPE) was selected as the source of SUP, and this study aimed to investigate the catalytic effects of the protonated CFA‐derived zeolite (H‐XA) as an economical option on the LDPE pyrolysis temperature and output. CFA converted into H‐XA through the conventional alkali fusion, followed by sonication and simplified hydrothermal and protonation processes. The impact of the alkali agent ratio on the resulting product was investigated, and outcomes were evaluated. The product with optimum properties was then selected for investigation in the LDPE pyrolysis studies. Finally, the results were compared with commercial Protonated Zeolite Socony Mobil‐5 (H‐ZSM5) and thermal decomposition without catalysts. Regarding LDPE degradation temperature, H‐XA could lower that by 97 °C compared to thermal degradation, which was almost the same as commercial H‐ZSM5 with 110 °C. The pyrograms obtained through the Pyrolysis‐gas chromatography‐mass spectrometry (Py‐GCMS) analysis indicated the elimination of heavier hydrocarbons in the presence of H‐XA and the product spectra laid in the range of C3 to C9, which was entirely different from the LDPE with hydrocarbons of varying lengths. Moreover, kinetic studies on the LDPE decomposition reactions in this work have revealed that LDPE conversion occurs at a lower activation energy level in the presence of H‐XA, which is comparable to the energy level observed when H‐ZSM5 is used as the catalyst. The synthesis of H‐XA with desirable catalytic activity, such as the ability to lower the LDPE degradation temperature and make lighter hydrocarbons as the pyrolysis output, suggests the great potential of the CFA‐based acid catalyst for use in SUP recycling. This represent a game of waste versus waste within the framework of the circular economy, where the environment is the ultimate winner. [ABSTRACT FROM AUTHOR]