This study explores the utilisation challenges of fly ash from municipal waste incineration, specifically focusing on ash from a dry desulphurisation plant (DDS), which is categorised as hazardous due to its high heavy metal content. The ash’s low silicon and calcium contents restrict its standalone utility. Laboratory investigations initially revealed that geopolymers derived solely from fly ash after flue gas treatment (FGT), in combination with coal combustion fly ash, exhibited low compressive strength (below 0.6 MPa). However, the study demonstrated significant improvements by modifying the FGT ash through water leaching. This process enhanced its performance when mixed with high-silica and -aluminium fly ash, resulting in geopolymers achieving compressive strengths of up to 18 MPa. Comparable strength outcomes were observed when the modified ash was blended with commercial cement. Leachability tests conducted for heavy metals (HMs) such as copper, zinc, lead, cadmium, and nickel indicated that their concentrations fell below the regulatory limits for landfill disposal: 2, 4, 0.5, 0.04, and 0.4 mg/kg, respectively. These results underscore the effectiveness of water-washing FGT ash in conjunction with other materials for producing geopolymers, contributing to sustainable waste management practices.

This paper presents the results of sorption tests against selected gaseous pollutants SO₂, CO₂ and H₂O on geopolymer materials obtained from high-calcium fly ash from lignite power generation. In the synthesis process, activation of geopolymer materials was carried out using KOH and NaOH. It was found that the activating agent significantly affects the porous structure of the samples. The sorption experiments conducted for the KOH-activated sample showed high SO₂ adsorption efficiency, almost ten times higher than against CO₂. The results demonstrate the possibility of utilizing fly ash obtained from the lignite energy processing sector for the synthesis of geopolymers with potential application of the materials as functional plastering compounds.

In this paper, the sorption of NH₃, H₂O, SO₂ and CO₂ was tested for several selected inorganic materials. The tests were performed on samples belonging to two topologies of materials, faujasite (FAU) and framework-type MFI, the structures of which differ in pore size and connectivity. All sorbates are important in terms of reducing their emissions to the environment. They have different chemical nature: basic, alkaline, and acidic. They are all polar in structure and composition and two of them (ammonia and water vapor) can form hydrogen bonds. These differences result in different interactions with the surface of the adsorbents. This paper presents experimental data and proposes a mathematical description of the sorption process. The best fit of the experimental data was obtained for the Toth and GAB models. The studies showed that among the selected samples, faujasite has the best sorption capacity for ammonia and water vapor, while the best sorbent for sulfur dioxide is the MFI framework type. These materials behave like molecular sieves and can be used for quite selective adsorption of relevant gases. In addition, modification of the faujasite with organic silane resulted in a drastic reduction in the surface area of the sorbent, resulting in significantly lower sorption capacities for gases.

The purpose of the article was to conduct an in-depth literature review on the possibilities of managing combustion by-products (mainly fly ash) in the context of a closed-loop economy. First, information on the chemical composition of fly ash in Poland was collected and compared with the composition of fly ash in other European countries. The authors concentrated on describing methods for synthesizing geopolymers and zeolites using fly ash as a substrate. By-products of zeolite synthesis, which are strongly alkaline solutions, can be used as a substrate in the synthesis of geopolymers. A concept has been proposed to combine the synthesis of zeolites and geopolymers into a single process to close the material loop. The search for comprehensive technological solutions that take into account the ideas of a closed-loop economy is essential in an era of resource depletion, and this literature review encapsulates this topic area.

Carbonaceous adsorbents have been pointed out as promising adsorbents for the recovery of methane from its mixture with carbon dioxide, including biogas. This is because of the fact that CO₂ is more strongly adsorbed and also diffuses faster compared to methane in these materials. Therefore, the present study aimed to test alternative carbonaceous materials for the gas separation process with the purpose of enriching biogas in biomethane and to compare them with the commercial one. Among them was coconut shell activated carbon (AC) as the adsorbent derived from bio-waste, rubber tire pyrolysis char (RPC) as a by-product of waste utilization technology, and carbon molecular sieve (CMS) as the commercial material. The breakthrough experiments were conducted using two mixtures, a methane-rich mixture (consisting of 75% CH₄ and 25% CO₂) and a carbon dioxide-rich mixture (containing 25% CH₄ and 75% CO₂). This investigation showed that the AC sample would be a better candidate material for the CH₄/CO₂ separation using a fixed-bed adsorption column than the commercial CMS sample. It is worth mentioning that due to its poorly developed micropore structure, the RPC sample exhibited limited adsorption capacity for both compounds, particularly for CO₂. However, it was observed that for the methane-rich mixture, it was possible to obtain an instantaneous concentration of around 93% CH₄. This indicates that there is still much potential for the use of the RPC, but this raw material needs further treatment. The Yoon–Nelson model was used to predict breakthrough curves for the experimental data. The results show that the data for the AC were best fitted with this model.