Biochars are increasingly used as soil amendment and for C sequestration in soils. The influence of feedstock differences and pyrolysis temperature on biochar characteristics has been widely studied. However, there is a lack of knowledge about the formation of potentially toxic compounds that remain in the biochars after pyrolysis. We investigated biochars from three feedstocks (wheat straw, poplar wood, and spruce wood) that were slowly pyrolyzed at 400, 460, and 525°C for 5 h (straw) and 10 h (woodchips), respectively. We characterized the biochars' pH, electrical conductivity, elemental composition (by dry combustion and X-ray fluorescence), surface area (by N adsorption), water-extractable major elements, and cation exchange capacity (CEC). We further conducted differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FTIR), and X-ray diffractometry to obtain information on the biochars' molecular characteristics and mineralogical composition. We investigated trace metal content, total polycyclic aromatic hydrocarbon (PAH) content, and PAH composition in the biochars. The highest salt (4.92 mS cm) and ash (12.7%) contents were found in straw-derived biochars. The H/C ratios of biochars with highest treatment temperature (HTT) 525°C were 0.46 to 0.40. Surface areas were low but increased (1.8-56 m g) with increasing HTT, whereas CEC decreased (162-52 mmol kg) with increasing HTT. The results of DSC and FTIR suggested a loss of labile, aliphatic compounds during pyrolysis and the formation of more recalcitrant, aromatic constituents. X-ray diffractometry patterns indicated a mineralogical restructuring of biochars with increasing HTT. Water-extractable major and trace elements varied considerably with feedstock composition, with trace elements also affected by HTT. Total PAH contents (sum of EPA 16 PAHs) were highly variable with values up to 33.7 mg kg; irrespective of feedstock type, the composition of PAHs showed increasing dominance of naphthalene with increasing HTT. The results demonstrate that biochars are highly heterogeneous materials that, depending on feedstock and HTT, may be suitable for soil application by contributing to the nutrient status and adding recalcitrant C to the soil but also potentially pose ecotoxicological challenges.

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The world's ever-growing energy demand will lead to the installation of new coal-fired power plants. At least part of the coal combustion residue (CCR) generated in the coming years will be disposed of, adding to the large number of CCR disposal sites generated in the past and reinforcing the need for sound assessment and management of associated risks. Physical and chemical composition of CCR varies considerably depending on the quality of the feed coal, the combustion technology, fraction considered, and the method of disposal. Related risk pathways include (i) aerial routes, i.e., dust resuspension (Cr(VI)), emanation of radioactivity (Rn associated with U and Th series), and Hg volatilization threatening animal and human health; (ii) phytoaccumulation (B, Se, Mo, As) and plant toxicity (B) with subsequent effects on animals (e.g., Mo-induced hypocuprosis, As and Se toxicity) and humans (e.g., selenosis; food chain); and (iii) effluent discharge and percolation to groundwater and rivers (suspended solids, unfavorable pH, high Se, B, Hg, and As(III) concentrations). Recent and projected changes of CCR composition due to emerging clean coal technologies require close monitoring as the concentration of volatile elements such as Hg and Se, solubility (Hg, Cd, Cu) and volatilization (Hg, NH(3)) of some pollutants are likely to increase because of higher retention in certain fractions of CCRs and concurrent changes in pH (e.g., by mineral carbonation) and NH(3) content. These changes require additional research efforts to explore the implications for CCR quality, use, and management of risk associated with disposal sites.

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