The gradients of root exudates and of persistent organic pollutants, including polycyclic aromatic hydrocarbons (PAHs), in rhizosphere soil in proximity to the root surface are still not well elucidated. In this work, a greenhouse experiment was conducted to investigate the distribution gradients of root exudates and phenanthrene and pyrene, as selected PAHs, in rhizosphere soil close to (0-8 mm) the root surface of ryegrass [Ldium multiflorum Lam.) as the host plant. Rhizosphere soil from the root surface (0-8 mm) was divided into three layers: the rhizoplane and strongly and loosely adhering soil. Root exudates were characterized as soluble organic C, organic acids, and total soluble sugars. In PAH-spiked rhizosphere soils, the concentration of root exudates decreased with distance from the roots. In a sterilized treatment, the amounts of root exudates in the three rhizosphere layers were higher than when the soil was not sterilized, indicating that microbial consumption contributed significantly to the loss of root exudates in the rhizosphere. Tlie residual concentrations of phenanthrene and pyrene clearly increased in die order of rhizoplane to loosely adhering soil after 40 to 50 d, which was significantly and negatively correlated with the amount of root exudates in the rhizosphere. In total, 87 to 97% of phenanthrene and 69 to 79% of pyrene dissipated in all three layers of rhizosphere soil after 40 d, and >99% of phenanthrene and 93% of pyrene dissipated after 50 d. The degradation ratio of PAHs decreased in rhizosphere soils with distance from the roots.Abbreviations: OA, organic acid; PAH, polycyclic aromatic hydrocarbon: SOC, soluble organic carbon: TSS,) total soluble sugar.

Soybean [Glycine max (L.) Merr.] stalk-based biochar was prepared using oxygen-limited pyrolysis. We evaluated phenanthrene (PHE) and Hg(II) sorption, from single and binary component solutions, onto prepared biochar. We found that the prepared biochar efficiently removed PHE and Hg(II) from aqueous solutions. The isotherms for PHE and Hg(II) sorption could be described using linear and Tóth models, respectively, both with high regression coefficients (R(2) > 0.995). When PHE and Hg(II) coexisted in an aqueous solution, we observed direct competitive sorption, each one suppressing another. Our results provide insight into the recycling of agricultural residues, and also a new application for removal of polycyclic aromatic hydrocarbons and heavy metals from contaminated water utilizing biochar from agricultural residue.

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This work explored the performance of sesame stalk-based carbon prepared at different carbonization temperatures and activated by potassium hydroxide in the removal of phenanthrene from an aqueous solution. At a carbon concentration of 10 mg/32 mL and a carbonization temperature of 7008C, the removal efficiency of phenanthrene approached 100%. Furthermore, with the presence of acenaphthene and naphthalene as co-contaminants, the removal efficiency of phenanthrene by the prepared carbon was 99.60%, which was comparable to that by the commercial carbon. Hydrophobic interactions influenced phenanthrene removal, and partitioning appeared to be the dominant mechanism for phenanthrene removal from aqueous solution by sesame stalk-based carbon. The results obtained from this work should provide insight into the reuse of agricultural residues, and also suggest a new avenue for the removal of polycyclic aromatic hydrocarbons from contaminated water utilizing carbon prepared from agricultural residue.

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A rapid method to determine chemical oxygen demand (COD) in printing and dyeing wastewater using ultraviolet (UV) spectroscopy was developed in this study. The UV method has several advantages compared to the chemical method, such as shortened analysis time, convenience, no requirement of expensive and toxic reagents, and good reproducibility. It was established that the magnitude of COD and, to a certain extent, pH and suspended solids of the sample have effects on the accuracy and precision of the method. The results showed the fitting range of CODCr (COD determined by the dichromate method) was 0 to 360 mg/L−1 And the pH ranged from 2.45 to 9.22. If the UV365 (UV absorbance at 365 nm) is measured and is subtracted from UV254 (UV absorbance at 254 nm), then the effects of suspended solids was eliminated. A control experiment of CODCr determination using the rapid method and the standard dichromate method was carried out, which validated the former.

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