Siderite (FeCO₃) is an iron-bearing carbonate mineral that is the most abundant sedimentary iron formation on Earth. Mineralogical alteration of four siderite samples annealed at temperatures 200 °C, 300 °C, 400 °C, 500 °C, 750 °C, and 1000 °C in an O₂ and a CO₂ atmosphere were investigated using such tools as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), the X-ray fluorescence (XRF) method, differential scanning calorimetry and thermogravimetric analysis (DSC/TGA), and Mössbauer spectroscopy measurements. The decomposition of three siderite samples with similar iron content in the oxygen atmosphere took place in the temperature range of 340–607 °C. This process begins at approximately ~100 °C higher under a reducing atmosphere, but it is completed just above 600 °C, which is a temperature comparable to decomposition in an oxidizing atmosphere. These processes are shifted toward higher temperatures for the fourth sample with the lowest iron but the highest magnesium content. Magnetite, hematite, and maghemite are products of siderite decomposition after annealing in the oxygen atmosphere in the temperature range 300–500 °C, whereas hematite is the main component of the sample detected after annealing at 750 °C and 1000 °C. Magnetite is the main product of siderite decomposition under the CO₂ atmosphere. However, hematite, maghemite, wüstite, and olivine were also present in the samples after annealing above 500 °C in this atmosphere.

The growing demand for rare-earth elements and yttrium (REY) in modern technologies has resulted in the systematic depletion of primary ores. For this reason, research is being conducted around the world on alternative sources of rare-earth elements, e.g., on the possibilities of recovering REY from coal waste or coal combustion. The article presents the results of comprehensive tests of the fuel—hard coal, and high-temperature HTA ash, fly ash, and bottom ash. Examined samples were taken from a Polish power plant. In the tests, fuel quality parameters were determined in accordance with the standards; microscopic observations in reflected and transmitted light, as well as a scanning electron microscope (SEM/EDS), were used, and chemical and phase composition were determined using ICP-MS and XRD methods, respectively. The distribution of REY between these ashes was analyzed. Their suitability as alternative sources of REY was assessed. The obtained results showed that the process of hard coal combustion in pulverized coal boilers influenced the geochemical differentiation of REY elements in energy waste. This differentiation is manifested by higher concentrations of REY and critical elements in the fly ash than in the bottom ash. The obtained values of the C_outl prospective coefficient made it possible to classify the analyzed fly and bottom ashes as prospective REY raw materials.

The aim of the research was to assess the potential of bottom ash from Polish coal-fired power plants as an alternative source of rare earth elements (REY). The potential of these ashes was compared with fly ash from the same coal combustion cycle. The phase and chemical composition, as well as REY, were determined using: X-ray diffraction and inductively coupled plasma mass spectrometry. The tested ashes were classified as inert-low pozzolanic and inert-medium pozzolanic, as well as sialic and ferrosialic, with enrichment in detrital material. The phase and chemical composition of bottom ash was similar to fly ash from the same fuel combustion cycle. The REY content in the ash was 199–286 ppm and was lower than the average for global deposits, and the threshold value was considered profitable for recovery from coal. Bottom ash’s importance as a potential source of REY will increase by recovering these metals from separated amorphous glass and mullite and grains rich in Al, Mg, K, and P. The industrial value of bottom ash as an alternative source of REY was similar to fly ash from the same fuel combustion cycle.

Rare earth elements are characterized by the high risk of their shortage resulting from limited resources. From this reason REE constitute a group of elements of special importance for the European Union. The aim of this study was to evaluate ashes from the burning of coal in fluidized bed boilers as an potential source of REY . Twelve samples of fly ash and bottom ash taken from power plants in Poland were analyzed. Tests have shown that despite some differences in chemical composition, the fly ash and bottom ash from fluidized beds could be classified as the calsialic, low acid type. It was found that fly ashes contained more REY than bottom ashes. Among REY , the light elements (LREY ) had the highest share in the total REY content in both fly ashes and bottom ashes. Heavy elements (HREY ) had the lowest content. The normalized curves plotted for fly ash samples within almost all of their entire range were positioned above the reference level and these curves were of the L-M or H-M type. The content of the individual REY in these samples was even twice as high as in UCC . The normalized curves plotted for bottom ash samples were classified as of L, L-M or H type. They were positioned on the reference level or above it. The content of the individual REY in these samples was the same or up to about 4 times lower than in UCC. It was found that the content of critical elements and of excessive elements in fly ash and bottom ash differs, which has an effect on the value of the outlook coefficient Coutl, and which is always higher in the case of fly ash than in the case of bottom ash. Nevertheless, the computed values of the outlook coefficient Coutl allow both fly ash and bottom ash from fluidized beds to be regarded as promising REY raw materials.