Phytoremediation of micropollutants by Phragmites australis, Typha angustifolia, and Juncus effuses.

Micropollutants (MPs) include organic chemicals, for example, pharmaceuticals and personal care products. MPs have been detected in the aquatic environment at low concentrations (ng/L-µg/L), which may lead to negative impacts on the ecosystem and humans. Phytoremediation is a green clean-up technology, which utilizes plants and their associated rhizosphere microorganisms to remove pollutants. The selection of plant species is important for the effectiveness of the phytoremediation of MPs. The plant species Phragmites australis, Typha angustifolia, and Juncus effuses are often used for MP removal. In this study, batch experiments were conducted to select plant species with an optimal ability to remove MPs, study the effect of temperature on MP removal in plants and the phytotoxicity of MPs. This study also explored the degradation of a persistent MP propranolol in plants in more detail. Data show that all three investigated plant species removed most MPs efficiently (close to 100 %) at both 10 and 21.5 °C. The tested plant species showed a different ability to translocate and accumulate propranolol in plant tissues. Typha angustifolia and Juncus effuses had a higher tolerance to the tested MPs than Phragmites australis. Typha angustifolia and Juncus effuses are recommended to be applied for phytoremediation of MPs.Novelty statement The novelty of this study is the selection of Typha angustifolia and Juncus effuses as proper plant species for phytoremediation of micropollutants (MPs). These two plant species were selected due to their good ability to remove MPs, tolerate low temperature, and resist the toxicity of MPs. The outcomes from this study can also be applied for constructed wetlands in removing MPs from wastewater. This study demonstrates the uptake and degradation processes of persistent MP propranolol in plants in more detail. Understanding the degradation mechanisms of a MP in plants is significant not only for the application of phytoremediation on MP removal but also for the development of constructed wetland studies.

Effect of electrolyte composition on electrochemical oxidation: Active sulfate formation, benzotriazole degradation, and chlorinated by-products distribution.

Electrochemical oxidation is an effective technique for treating persistent organic pollutants, which are hardly removed in conventional wastewater treatment plants. Sulfate and chloride salts commonly used and present in natural wastewater influence the electrochemical degradation process. In this study, the effect of electrolyte composition on the active sulfate species (SO4●⁻ and S2O82⁻) formation, benzotriazole degradation-a model organic compound, and chlorinated by-products distribution have been investigated while using a boron-doped diamond (BDD) anode. Different Na2SO4:NaNO3 and Na2SO4:NaCl ratios with constant conductivity of 10 mS/cm were used in the experiments and applied anode potential was kept constant at 4.3 V vs. Ag/AgCl. The electrogenerated SO4●⁻ and S2O82⁻ formation were faster in 10:1 and 2:1 Na2SO4:NaNO3 ratios than in the 1:0 ratio. The ●OH-mediated SO4●⁻ production has prevailed in 10:1 and 2:1 ratios. However, ●OH-mediated SO4●⁻ production has hindered the 1:0 ratio due to excess chemisorption of SO42⁻ on the BDD anode. Similarly, the faster benzotriazole degradation, mineralization, and lowest energy consumption were achieved in the 10:1 Na2SO4:NaNO3 and Na2SO4:NaCl ratio. Besides, chlorinated organic by-product concentration (AOX) was lower in the 10:1 Na2SO4:NaCl ratio but increased with the increasing chloride ratio in the electrolyte. LC-MS analysis shows that several chlorinated organic transformation products were produced in 0:1 to 2:1 ratio, which was not found in the 10:1 Na2SO4:NaCl ratio. A comparatively higher amount of ClO4⁻ was formed in the 10:1 ratio than in 2:1 to 0:1 ratio. This ClO4⁻ formation train evidence the effective ●OH generation in a sulfate-enriched condition because the ClO4⁻ formation is positively correlated to ●OH concentration. Overall results show that sulfate-enriched electrolyte compositions are beneficial for electrochemical oxidation of biorecalcitrant organic pollutants.

Water-Based Synthesis of Hydrophobic Ionic Liquids [N8888][oleate] and [P666,14][oleate] and their Bioprocess Compatibility.

The conversion of organic waste streams into carboxylic acids as renewable feedstocks results in relatively dilute aqueous streams. Carboxylic acids can be recovered from such streams by using liquid-liquid extraction. Hydrophobic ionic liquids (ILs) are novel extractants that can be used for carboxylic acid recovery. To integrate these ILs as in situ extractants in several biotechnological applications, the IL must be compatible with the bioprocesses. Herein the ILs [P666,14][oleate] and [N8888][oleate] were synthesized in water and their bioprocess compatibility was assessed by temporary exposure to an aqueous phase that contained methanogenic granular sludge. After transfer of the sludge into fresh medium, [P666,14][oleate]-exposed granules were completely inhibited. Granules exposed to [N8888][oleate] sustained anaerobic digestion activity, albeit moderately reduced. The IL contaminants, bromide (5-500 ppm) and oleate (10-4000 ppm), were shown not to inhibit the methanogenic conversion of acetate. [P666,14] was identified as a bioprocess-incompatible component. However, our results showed that [N8888][oleate] was bioprocess compatible and, therefore, has potential applications in bioprocesses.