Graphitic carbon nitride (g-C₃N₄) proved to be a promising semiconductor for the photocatalytic degradation of various organic pollutants. However, its efficacy is limited by a fast electron hole recombination, a restricted quantity of active sites, and a modest absorption in the visible range. To overcome these limitations, g-C₃N₄-Bi₂S₃ and g-C₃N₄-ZnS composites were effectively produced utilizing a starch-assisted technique. The findings from FT-IR, XRD, EDX, XPS, BET, SEM, and TEM demonstrated that the enhanced photocatalytic activity of g-C₃N₄-Bi₂S₃ and g-C₃N₄-ZnS composites was primarily due to their improved photocarrier separation and transfer rates. The photocatalyst facilitated the aerobic photocatalytic degradation of colorless contaminants such as coumarin and para-nitrophenol (4-NP). For the decomposition of 4-NP, g-C₃N₄-Bi₂S₃ exhibited a maximum efficiency of 90.86% in UV light and 16.78% in visible light, with rate constants of 0.29 h⁻¹ and 0.016 h⁻¹, respectively. In contrast, g-C₃N₄-ZnS demonstrated a maximum efficiency of 100% in UV light and 15.1% in visible light, with rate constants of 0.57 h⁻¹ and 0.018 h⁻¹, respectively. The bioinspired synthesis combined with the modification with metal sulfides proved to considerably enhance the photocatalytic activity of g-C₃N₄, increasing its potential for practical applicability in environmentally friendly water treatment systems for the efficient removal of recalcitrant organic contaminants.

At present, to achieve further reductions in CO₂ emissions in the cement industry, it is essential to improve the efficiency of grinding processes and reduce the energy demand. This study examined the effects of various grinding parameters (addition of trass, ball to powder mass ratio (BPR), material of grinding bodies and jars, rotational speed, and mill type) to minimize the energy consumption of the mechanochemical activation of kaolinite. X-ray diffraction, Fourier transform infrared spectroscopy, inductively coupled plasma optical emission spectroscopy, scanning electron microscopy, and specific surface area measurements were used to examine the influence of grinding parameters. It was found that the addition of as little as 25% (mass percent) trass reduced the specific energy demand for the complete amorphization of kaolinite by 56%. The application of steel grinding bodies (instead of ZrO₂ ones) had a slight influence on the amorphization kinetics of kaolinite, but it could mechanochemically activate 30% more samples at the same BPR and specific energy demand. The use of the four-pot milling instead of the one-pot could considerably decrease the specific energy demand of the complete and incomplete (α = 0.9) amorphization of kaolinite. Overall, a 94% reduction was achieved in specific energy demand with steel grinding material, 14:1 BPR, four-pot milling, and the incomplete amorphization of kaolinite.

The availability of industrially used supplementary cementitious materials (SCMs, e.g., fly ash) decreases due to the rise in renewable energy sources and recycling technologies. Therefore, it is essential to find alternative SCMs (e.g., waste glass and clay brick powder) that are locally available. Accordingly, in this paper, the mechanochemical activation of clay brick waste (CBW) with abrasive glass powder (GP) and its pozzolanic reactivity are investigated. The mixtures of CBW and GP in mass ratios of 100:0, 75:25, 50:50, and 25:75 were mechanochemically activated for 15, 30, 45, and 60 min. The physical, chemical, and structural changes of the mixtures were examined by X-ray diffractometry, Fourier-transform infrared spectroscopy, scanning electron microscopy, and specific surface area measurements. The pozzolanic reactivity was characterized by the active silica content and the 28-day compressive strength of the binders (a mixture of ordinary Portland cement and activated material). The addition of GP favorably reduced the agglomeration and increased the active silica content of the activated mixtures (e.g., by 7–37% m/m at 15 min of mechanochemical activation). The 60 min of mechanochemical activation and the addition of 50% m/m of GP can increase the compressive strength by approximately 8%. Economically, the addition of 50% m/m of GP was found to be favorable, where only 30 min of mechanochemical activation resulted in a considerable increase in strength compared to that of the ordinary Portland cement.

Kaolin-based graphitic carbon nitride (g-CNx) composite photocatalysts were synthesized from a urea precursor using a commercial kaolin. Structural characterization by X-ray diffraction and infrared spectroscopy (FTIR) verified the successful thermal polycondensation of g-CNx along the thermal dehydroxylation of kaolinite to metakaolin at 550 °C. The g-CNx content of the composites were estimated by thermogravimetry and CHN analysis, ranging from ca. 87 m/m% to ca. 2 m/m% of dry mass. The addition of kaolin during the composite synthesis was found to have a significant effect: the yield of in situ formed g-CNx drastically decreased (from ca. 4.9 m/m% to 3.8–0.1 m/m%) with increasing kaolin content. CHN and FTIR indicated the presence of nitrogen-rich g-CNx, having a specific surface area of 50 m²/g, which synergistically increased after composite synthesis to 67–82 m²/g. Estimated optical band gaps indicated the affinity to absorb in the visible light spectrum (λ < 413 nm). Photocatalytic activity upon both UV and artificial sunlight irradiation was observed by hydroxyl radical evolution, however, without the synergistic effect expected from the favorable porosity.