This study aims to investigate the effects of ammonium-bearing zeolitic waste (FCC) on alkali-activated biomass bottom ash (BBA). FCC was obtained from the oil-cracking process in petroleum plants. In this study, two types of production waste were used: biomass bottom ash and ammonium-bearing zeolitic waste. These binary alkali-activated FCC/BBA blends were investigated using X-ray diffraction (XRD), Fourier transform infrared (FTIR) and scanning electron microscopy (SEM) methods. The compressive strength of the hardened samples was evaluated. The results show that the samples made from alkali-activated BBA biomass bottom ash had low (8.5 MPa) compressive strength, which could be explained with low reactive BBA and insufficient quantities of silicon and aluminum compounds. The reactivity of BBA was improved with incorporating zeolitic waste as an aluminosilicate material. This zeolitic waste was first used for ammonium sorption; then, it was incorporated in alkali-activated samples. Additional amounts of hydrated products formed, such as calcium silicate hydrate, calcium aluminum silicate hydrate and calcium sodium aluminum silicate hydrate. The silicon and aluminum compound, which varied in zeolitic waste, changed the mineral composition and microstructure of alkali-activated binder systems. NH₄Cl, which was incorporated in the zeolitic waste, did not negatively affect the compressive strength of the alkali-activated BBA samples. This investigation proved that waste materials can be reused by producing alkali-activated binders.

Fluid catalytic cracking (FCC) catalysts, used in the petroleum industry, are sources of zeolitic by-products. These by-products are often used as sorbents for the removal of ammonium ions from wastewater. After a period of use, the zeolitic by-product loses its sorption properties and is no longer effective. The problem is the use of zeolitic by-product with ammonium ions. In this study, a zeolitic by-product containing ammonium ions and high contents of active SiO₂ and Al₂O₃ was used as a supplementary cementitious material (SCM). Cement pastes containing 0.5%, 1%, 3%, 5%, and 10% of the by-product were prepared, and the compressive strength and density of the pastes were evaluated. Incorporation of the zeolitic by-product increased the cement strength by 17% and 32% after 7 and 28 days of hydration, respectively. Thus, incorporation of the zeolitic by-product with ammonium ions as an SCM has a complex effect on an ordinary Portland cement (OPC) system. Ammonium chloride accelerated cement setting after 7 days of hydration, and the pozzolanic reaction positively affected strength development after 28 days of hydration. The reaction products caused the cement to have a compact microstructure. The zeolitic by-product containing absorbed ammonium ions can be successfully reused to replace ordinary Portland cement in cement pastes.

In this study, straetlingite-based sorbents were used for NH₄⁺ ion removal from a synthetic aqueous solution and from the wastewater of an open recirculation African catfish farming system. This study was performed using column experiments with four different filtration rates (2, 5, 10, and 15 mL/min). It was determined that breakthrough points and sorption capacity could be affected by several parameters such as flow rate and mineral composition of sorption materials. In the synthetic aqueous solution, NH₄⁺ removal reached the highest sorption capacity, i.e., 0.341 mg/g with the S30 sorbent at a filtration rate of 10 mL/min and an initial concentration of 10 mg/L of NH₄⁺ ions. It is important to emphasize that, in this case, the Ce/C0 ratio of 0.9 was not reached after 420 min of sorption. It was also determined that the NH₄⁺ sorption capacity was influenced by phosphorus. In the wastewater, the NH₄⁺ sorption capacity was almost seven times lower than that in the synthetic aqueous solution. However, it should be highlighted that the P sorption capacity reached 0.512 mg/g. According to these results, it can be concluded that straetlingite-based sorbents can be used for NH₄⁺ ion removal from a synthetic aqueous solution, as well as for both NH₄⁺ and P removal from industrial wastewater. In the wastewater, a significantly higher sorption capacity of the investigated sorbents was detected for P than for NH₄⁺.