A total solution for the utilisation of BFS can be achieved and the resulting valuable products CaMgAl-LDHs and MCM-41 are promising sorbents for CO₂ capture.

A porous geopolymer with adsorption and photocatalytic degradation functions was successfully developed by utilizing Ti-bearing blast furnace slag (TBBFS) as the raw material. The prepared porous geopolymers were characterized by X-ray diffraction, scanning electron microscope, energy dispersive spectrometer, and Fourier transform infrared spectrum. Selective crystallization, water quenching, and natural cooling methods were employed to investigate the influences of these modifications on the applicability of TBBFS as a precursor for geopolymer synthesis. Water-quenched slag with amorphous content was prone to alkali dissolution, and the resulting geopolymer exhibited the highest adsorption capacity (97.18 mg/g) for methylene blue (MB) removal. Selective crystallization at 1400 °C generated a hybrid microstructure consisting of a non-cementitious CaTiO₃ crystallization phase and a cementitious amorphous fraction. The retention of CaTiO₃ in the final geopolymer enables a bifunctionality in adsorption–photodegradation. Particularly, the adsorption and photodegradation processes under various conditions were investigated. The superior removal efficiency for MB could be attributed to the synergistic effects between the geopolymer matrix and CaTiO₃, leading to an enhancement in the formation of hydroxyl radicals. The conversion of TBBFS into porous geopolymer offers an efficient and straightforward solution for slag utilization and dye removal.

In this paper, high value added NaA zeolite material was prepared from blast furnace (BF) slag by hydrothermal method and its adsorption behavior on the removal of ammonium ion was investigated. It was found out that the synthetic NaA cubic zeolite with smaller crystal size obtained at nSiO₂/nAl₂O₃ = 2 and nH₂O/nNaOH = 20 showed better adsorption performance. The kinetics of the adsorption of ammonium ion by synthesized NaA zeolite was fitted by the pseudo-second-order kinetic model. The intra-particle diffusion modeling reveals that two mixed rate-controlling mechanisms were involved in the adsorption process. The relatively high value of activation energy of 92.3 kJ·mol⁻¹ indicates a high impact of temperature on the adsorption rate, and the nature of ammonium adsorption is chemical reaction rather than physisorption. Based on the thermodynamics calculations, the adsorption of ammonium was found to be an endothermic, spontaneous process. The adsorption isothermal analysis showed that the Langmuir model could be well fitted and a maximum adsorption capacity of 83.3 mg·g⁻¹ of NH₄⁺ was obtained. Thus, it was demonstrated that by forming low cost NaA zeolite and using it for environmental remediation, the synchronous minimization of BF slag and ammonia nitrogen contamination could be achieved.

The fabrication of well densified wollastonite with smooth appearance by direct sintering method is still a challenge due to the competitive behaviors between sintering and crystallization. In this study, the coarser glass frits with a size of 1–4 mm are subjected to heat treatment at different temperatures. An attempt of integrating differential thermal analyzer with a slag melting temperature characteristic tester was exploited to monitor the heat and geometry changes during the heating. The results showed that the addition of CaF₂ can significantly promote the crystallization of wollastonite at 940 °C, while hindering the sintering ability. At higher temperature, the increase of CaF₂ acts as flux and favors the formation of eutectics, leading to a decline in the precipitation amount of wollastonite. The predominated liquid sintering brought fast shrinkage. It was found out that high content of CaF₂ narrows the dense sintering temperature range and results in uneven surfaces. In order to obtain wollastonite glass-ceramics with smooth appearance, the maximum content of CaF₂ in sintering glass-ceramics should be limited to 2 wt.%.