Fossil fuels, especially coal, have played a pivotal role in driving technological and economic advancements over the past century, though accompanied by numerous environmental challenges. Rapid progress in green and sustainable energy sources, including tidal, wind, and solar energy, coupled with growing environmental concerns, the conventional coal industry is experiencing a sustained decline in both size and financial viability. This situation necessitates the urgent adoption of advanced approaches to coal utilization. Beyond serving as an energy source, coal and its by-products, known as coal waste, can serve as valuable resources for the development of advanced materials, including photocatalysts. The advancement of photocatalytic materials derived from coal and coal waste can capitalize on these natural carbon and mineral sources, providing a viable solution to numerous environmental challenges. Currently, research in this domain remains in its early stages, with existing studies primarily focusing on specific types of photocatalysts or particular aspects of the fabrication process. Therefore, available coal-based and coal waste-based photocatalytic materials were systematically examined and categorized into six types according to their composition and dimensional/structural characteristics. Each type of photocatalytic material was introduced, along with common fabrication and characterization technologies. Representative works were discussed in detail to highlight the unique features of different types of coal-based and coal waste-based photocatalytic materials. Furthermore, the promising applications of these materials in environmental protection and pollution treatment were summarized, while also addressing the challenges and prospects in this research field. This review comprehensively overviews the fundamental knowledge and recent advancements in photocatalytic materials derived from coal and coal waste, with the goal of catalyzing the development of next generation photocatalysts and contributing to the transformation of the conventional coal industry.

This paper aims at synthesizing the scientific research on coal fly ash and agriculture using bibliometric analysis. The research on fly ash and agriculture has grown at 6.7% annually during 1973-2022, where much attention has been received after 2007. The number of publications on coal fly ash and agriculture reached above 100 in the year 2010, which further increased to 299 by 2020. The research productivity has been assessed as the most influential countries, journals, and documents in terms of a number of publications and citations on fly ash and agriculture. India is the most productive country in terms of knowledge on coal fly ash and agriculture with 38% of the global publications, while Environmental Science and Pollution Research is the leading journal with 19 publications. The article on assessing the impact of fly ash incorporation in soil systems by Pandey and Singh (2010), having 349 citations with 26.85 citations per year is one of the leading publications globally. Further, science mapping has been conducted to comprehend the current research focus and discover the emerging themes for future research. The finding of the thematic map based on the level of development and importance indicate that FA can be effectively explored as soil-additive for improved physical, chemical and biological properties and enhanced plant nutrients. The findings provide several aspects of fly ash and suggest future research directions to study the potential of using coal fly ash in agriculture to gain an agronomic advantage.

The effectiveness and longevity of permeable reactive barriers (PRBs) depend on the performance of the reactive materials and the subsurface environment. The relationship of the groundwater velocity on performance of coal waste for the heavy metal removal was reported in our previous study. In this study, we investigated the performance and longevity of coal waste as a PRB material for the removal of Cd considering subsurface environmental conditions such as contamination level and groundwater velocity. The artificial groundwater contaminated by Cd were prepared with various concentrations ranging from 10 to 100 mg L-1. Lab-scale column experiments were conducted using coal waste filled columns by injecting the artificial groundwater. The breakthrough curves were analyzed advection dispersion equation coupled with equilibrium sorption model to determine the retardation factor. The Cd breakthrough curves exhibited different retardation with respect to the contamination levels. The Cd transport was more retarded as the contamination level lowered. The relationship between the retardation factor and the contamination levels could be explained with empirical equations based on non-linear sorption isotherms. By adopting the velocity dependency of sorbent performance in our previous study, transport of Cd within coal waste was simulated under various subsurface environmental conditions to construct the longevity function. The function could be used for the longevity prediction of coal waste as a PRB material considering groundwater velocity and contamination level in subsurface environment.

A simple mixing-pressing followed by thermal curing and pyrolysis process was used to upcycle coal waste into high-value composites. Three coal wastes of different physicochemical properties were investigated. The hypothetical mechanisms of bonding between the coal particles and the preceramic polymer are presented. The textural properties of the coals indicated that the lowest volatile coal waste (PCD) had a dense structure. This limited the diffusion and reaction of the preceramic polymer with the coal waste during pyrolysis, thereby leading to low-quality composites. The water contact angles of the composites up to 104° imply hydrophobic surfaces, hence, no external coating might be required. Analysis of the carbon phase confirmed that the amorphous carbon structure is prevalent in the composites compared to the coal wastes. The dc volume resistivity of the composites in the range of 22 to 82 Ω-cm infers that the composites are unlikely to suffer electrostatic discharge, which makes them useful in creating self-heating building parts. The leached concentrations of heavy metal elements from the composites based on the end-of-life scenario were below the Toxicity Characteristic Leaching Procedure regulatory limits. Additionally, the release potential or mobility of the metals from the composites was not influenced by the pH of the eluants used. On the basis of the reported results, these carbon/ceramic composites show tremendous prospects as building materials due to these properties.

Coal waste composed of naturally occurring minerals is applicable as a reactive medium to permeable reactive barriers due to its reactivity to heavy metals. In this study, we evaluated the longevity of coal waste as PRB media to control heavy metal-contaminated groundwater considering variable groundwater velocity. Breakthrough experiments were conducted using coal waste-filled column by injecting artificial groundwater, 10 mg/L of cadmium solution. The artificial groundwater was fed to the column at different flow rates to mimic a wide range of porewater velocities in the saturated zone. The reaction between cadmium breakthrough curves was analyzed using a two-site nonequilibrium sorption model. The cadmium breakthrough curves showed a significant retardation, which increased with decreasing porewater velocity. The greater the retardation, the longer the longevity of coal waste could be expected. The greater retardation under a slower velocity environment was due to the higher fraction of equilibrium reaction. The nonequilibrium reaction parameters could be functionalized with respect to the porewater velocity. The simulation of contaminant transport using the reaction parameters could be used as a method to evaluate the longevity of the pollution-blocking material in an underground environment.

The global coal industry yields a vast amount of tailings waste, and the utilisation of these tailings necessitates innovative efforts contributing to the United Nations Sustainable Development Goals. One of such novel initiatives is to reuse coal tailings (CT) safely, ecofriendly, and cost-effectively in agroecosystems as a soil conditioner to enhance the productivity of lands. This study aimed to evaluate the potential utilisation of coal tailings waste in the soil amelioration to improve plant performance. The physico-chemical characteristics of coal tailings from two Australian mining sites (CT1 and CT2) showed that the tailings samples are alkaline with loamy and loamy sand textures, respectively. The tailings have ~ 3% of macronutrients, high carbon (C), and low heavy metals and metalloids (As, Cd, Se, Cu, Zn, and Pb). The germination rate of tomato seeds was improved in the low-rate CT treatment. Greenhouse tomato plants exhibited an increase in leaf\'s K, Ca, and Mg contents in CT1 and CT2 treatments. More importantly, the CT treatment-induced accumulation of heavy metals in plants was mostly insignificant in both CT treatments. Therefore, we highlight the potential application of coal tailings as a soil conditioner because of the beneficial effect of improved carbon and nutrients (N, P, K, Mg, and Ca) in tomato leaves. Further amendment of the coal tailings should focus on the adjustment of pH and the addition of other beneficial materials for the improvement of soil properties for crops in both the greenhouse and the field.

Selenium (Se) has been mobilised by leaching from coal and associated waste rock exposed by mining activities in Western Canada, with deleterious impact on aquatic wildlife. Waste rock characterisation indicates that up to 7% of the Se, as Se(IV), may be associated with organic matter, with ≈9%, as Se(0), associated with euhedral pyrite. Small 1-2 µm mineral particles with average Se concentration of 1.0 ± 0.4 wt% account for the remaining Se with the largest components likely to be associated with Fe oxide/hydroxide/carbonate as Se(0) and framboidal pyrite as Se(IV) and Se(0). No evidence was found for the presence of Se(-I), Se(-II) or Se(VI). In the first 8 weeks of leaching Se release was not correlated to the addition of aqueous silicate, added to aid pyrite passivation, but was reduced by approximately one third when the waste was treated with manure. This suggests the primary initial source of leached Se was not pyrite. Added organic C results in increased microbial numbers, particularly aerobic microbes, and promotes the formation of extensive coating of extracellular polymeric substances resulting in depletion of O2 at particle surfaces, reducing oxidation of Se(IV) and therefore reducing the leach rate of Se. Subsequent to 8 weeks of leaching the rates of release of Se from the treated wastes were similar regardless of treatment strategy but were reduced as compared to the untreated waste rock, suggestive of partial framboidal pyrite geochemical and microbial passivation. Se leaching was not correlated to S leaching, but the source(s) of the leached S was not known as approximately half of the S within the waste rock was non-sulfidic. These results indicate that utilisation of local organic carbon-containing wastes for coverage of coal waste rock may be a cost-effective strategy to reduce Se leaching to acceptable rates of release regardless of whether the Se is associated with framboidal pyrite or organics.

Pyrite-bearing coal wastes are responsible of the formation of acid mine drainage (AMD), and their management to mitigate environmental impacts is a challenge to the coal mine industry in Europe and worldwide. The European CEReS project sought to develop a generic co-processing strategy to reuse and recycle coal wastes, based on removal of AMD generating potential through bioleaching. Chemolitoautotrophic iron- and sulfur-oxidizing microbial consortia were enriched from a Polish coal waste at 30 °C and 48 °C, but not 42 °C. Pyrite leaching yield, determined from bioleaching tests in 2-L stirred bioreactors, was best with the 48 °C endogenous consortium (80%), then the 42 °C exogenous BRGM-KCC consortium (71%), and finally the 30 °C endogenous consortium (50%). 16S rRNA gene-targeted metagenomics from five surface locations on the dump waste revealed a microbial community adapted to the site context, composed of iron- and/or sulfur-oxidizing genera thriving in low pH and metal rich environments and involved in AMD generation. All together, the results confirmed the predisposition of the pyritic coal waste to bioleaching and the potential of endogenous microorganisms for efficient bioleaching at 48 °C. The good leaching yields open the perspective to optimize further and scale-up the bioleaching process.

It is necessary to determine an environmentally friendly method of reusing the vast amount of coal waste that is generated during coal preparation. This study evaluates the applicability of using weathered coal waste in a permeable reactive barrier to prevent groundwater contamination. Coal waste, with different weathering degrees, was obtained from two coal mining sites in South Jeolla Province, Korea. The reactivities of the coal waste with inorganic contaminants, such as copper, cadmium, and arsenic, were examined in batch and column experiments. The batch experiment results indicate that the coal waste removal efficiencies of copper (99.8%) and cadmium (95.4%) were higher than those of arsenic (71.0%). The maximum adsorption capacities of coal waste for copper, cadmium, and arsenic calculated from the Langmuir isotherm model were 4.440 mg/g, 3.660 mg/g, and 0.718 mg/g, respectively. The equilibrium of adsorption was attained within 8 h. The column experiment results reveal that the coal waste effectively removed inorganic contaminants under flow-through conditions. Faster breakthrough times were observed in single solute system (As(V) = 19.3 PV, Cu(II) = 47.6 PV) compared with binary solute system (As(V) = 27.8 PV, Cu(II) = 65.4 PV). To confirm the applicability of using coal waste in a groundwater environment, its decontamination ability was analyzed at low concentrations and under various pH conditions. To examine the potential ecological risks in the subsurface environment, a test to determine acute toxicity to Daphnia magna and a toxic characteristic leaching procedure (TCLP) test were conducted. The coal waste was found to satisfy appropriate standards. The acute toxicity test also confirmed the ecological safety of using coal waste in a groundwater environment. The acceptably high capacity and fast kinetics of inorganic contaminant sorption by the coal waste indicate it could potentially be employed as a reactive material. The recycling and application of this abundant waste material will contribute to solving both coal waste disposal and water pollution problems.

A sample coal waste activated by rhamnolipid biosurfactants was used as an efficient adsorbent for the adsorption of cadmium from aqueous solution. The effects of three factors, namely, initial solution pH (3-11), absorbent to cadmium ratio (12.5-162.5) and contact time (3-31 h), on cadmium removal were studied and optimized using a central composite type response surface methodology. The two factors that play a key role in the adsorption process are pH and absorbent dosage. Optimum adsorption conditions achieved at pH 9, absorbent to cadmium ratio of 125 and equilibrium contact time of 10 h, resulted in more than 99% cadmium removal. Kinetic studies revealed that a maximum removal can be achieved before 10 min of adsorption process following a pseudo-second order model. The selectivity study in bimetal aqueous systems using copper, lead and zinc metals showed the adsorption order of Cu2+ > Cd2+ > Zn2+ > Pb2+. The cadmium adsorption on activated coal waste was also found to follows the Temkin isotherm model with a correlation coefficient of 92.43%.