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Unconventional substrata like activated carbon or clay beads can enhance micropollutant removal in constructed wetlands. However, hydroponic materials widely used in horticulture have not yet been investigated for their potential to remove micropollutants. In addition, potential effect of plant species other than reeds on micropollutant removal has not been sufficiently investigated. Therefore, a nature-based, post-treatment technology called improved vertical flow constructed wetlands (CW) with hydroponic (H) materials (CWH) was designed by employing cocopeat and mineral with ornamental plant species syngonium and periwinkle. A mesocosm CWH system was tested in a climate-controlled greenhouse for 550 days for its potential to remove frequently found micropollutants in wastewater, namely sulfamethoxazole, trimethoprim, diclofenac, erythromycin, carbamazepine, pyrimethanil, tebuconazole, pymetrozine, atrazine and DEET from wastewater effluent. The main focus was to understand the contribution of sorption, microbial degradation and phytoremediation on the removal of those micropollutants. It was found that cocopeat showed a capacity for sorbing micropollutants, ranging between 80 and 99% of the compounds added while less than 10% sorption was observed for mineral wool. Additionally moderate to high biological removal (25-60 μg of compound/kg dry weight of substratum/day) for most of the studied compounds was observed in all the cocopeat biotic groups. Furthermore, it could be stated that plants appear not to be an important factor for micropollutant removal. The observed differences in removal between the cocopeat and mineral wool systems could be explained by the difference in physico-chemical properties of the substrata, where cocopeat has a higher water holding capacity, moisture content, nutrient and organic matter content, and a higher intraparticle porosity and surface area. This study revealed notable removal of persistent and mobile micropollutants in cocopeat CWH, namely carbamazepine (80-86%) and diclofenac (97-100%). These results demonstrate the potential beneficial use of hydroponic materials as substratum in more advanced constructed wetlands designed to remove micropollutants., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Groundwater, a major source of drinking water worldwide, is often contaminated with micropollutants. Although microbial communities in aquifers and soils have the capability to biodegrade some micropollutants, this process is limited in situ. Biostimulation with dissolved organic carbon (DOC) is known to promote micropollutant biodegradation, but the role of DOC biodegradability is still poorly understood. This study investigated how three DOC types with different biodegradability (humics, dextran and acetate) affect the biodegradation of 15 micropollutants by aquifer and soil microbial communities under aerobic and nitrate reducing conditions. Although originating from different environments, both communities were able to biodegrade the same 4 micropollutants under aerobic conditions - 2,4-D, MCPP, chloridazon (CLZ) and chloridazon-desphenyl. However, DOC addition only affected MCPP biodegradation, promoting MCPP biodegradation regardless of DOC biodegradability. Biodegradation of 2,4-D, MCPP and CLZ under aerobic conditions was observed after a lag phase, whose duration differed per compound. 2,4-D was biodegraded first and fully. Aquifer community was able to degrade about half of the initial MCPP concentration (removal efficiency of 49.3 ± 11.7%). CLZ was fully biodegraded by the aquifer community, but not by the soil community, possibly due to substrate competition with organics originating from the inoculum. Therefore, the natural organic carbon present in the inocula and in environmental systems can influence micropollutant biodegradation. Under nitrate reducing conditions micropollutant biodegradation was not observed nor biostimulated by DOC addition. The results also highlight the importance of sufficient exposure time to trigger in situ micropollutant biodegradation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Groundwater is the main source for drinking water production globally. Groundwater unfortunately can contain micropollutants (MPs) such as pesticides and/or pesticide metabolites. Biological remediation of MPs in groundwater requires an understanding of natural biodegradation capacity and the conditions required to stimulate biodegradation activity. Thus, biostimulation experiments are a valuable tool to assess pesticide biodegradation capacity of field microorganisms. To this end, groundwater samples were collected at a drinking water abstraction aquifer at two locations, five different depths. Biodegradation of the MPs BAM, MCPP and 2,4-D was assessed in microcosms with groundwater samples, either without amendment, or amended with electron acceptor (nitrate or oxygen) and/or carbon substrate (dissolved organic carbon (DOC)). Oxygen + DOC was the most successful amendment resulting in complete biodegradation of 2,4-D in all microcosms after 42 days. DOC was most likely used as a growth substrate that enhanced co-metabolic 2,4-D degradation with oxygen as electron acceptor. Different biodegradation rates were observed per groundwater sample. Overall, microorganisms from the shallow aquifer had faster biodegradation rates than those from the deep aquifer. Higher microbial activity was also observed in terms of CO 2 production in the microcosms with shallow groundwater. Our results seem to indicate that shallow groundwater contains more active microorganisms, possibly due to their exposure to higher concentrations of both DOC and MPs. Understanding field biodegradation capacity is a key step towards developing further bioremediation-based technologies. Our results show that biostimulation has real potential as a technology for remediating MPs in aquifers in order to ensure safe drinking production., (Copyright © 2021 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

DNA-stable isotope probing (SIP) with 13 C labeled phenanthrene (PHE) as substrate was used to identify specific bacterial degraders during natural attenuation (NA) and bioaugmentation (BA) in petroleum contaminated soil. BA, with the addition of a bacterial suspension mixture named GZ, played a significant role in PHE degradation with a higher PHE removal rate (∼90%) than that of NA (∼80%) during the first 3 days, and remarkably altered microbial communities. Of the five strains introduced in BA, only two genera, particularly, Ochrobactrum, Rhodococcus were extensively responsible for PHE-degradation. Six (Bacillus sp., Acinetobacter sp., Xanthomonas sp., Conexibacter sp., Acinetobacter sp. and Staphylococcus sp.) and seven (Ochrobactrum sp., Rhodococcus sp., Alkanindiges sp., Williamsia sp., Sphingobium sp., Gillisia sp. and Massilia sp.) bacteria responsible for PHE degradation were identified in NA and BA treatments, respectively. This study reports for the first time the association of Xanthomonas sp., Williamsia sp., and Gillisia sp. to PHE degradation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

The reuse of cooling tower blowdown (CTBD) in the cooling tower itself requires CTBD deionization and a pre-treatment before deionization to remove organic compounds (OCs) that induce membrane fouling. This study assesses the potential of electrochemical oxidation (EO) with a boron-doped diamond (BDD) and a Ti/RuO 2 mixed-metal oxide (MMO) anode for CTBD pre-treatment. Also, the influence of the applied current density (j), initial pH, hydrodynamic conditions, and supporting electrolyte on the process performance was evaluated. Results show that COD and TOC removal were 85 and 51%, respectively, with the BDD-anode; however, they were 50 and 12% with MMO-anode at a j-value of 8.7 mA cm -2 and neutral pH. An increased j-value increased the COD and TOC removal; however, different pHs, hydrodynamic conditions, and the addition of supporting electrolytes had a minor impact on the removal with both anodes. Liquid chromatography-organic carbon detection analysis showed that the OC in CTBD mainly consisted of humic substances (HS). EO with the BDD-anode resulted in 35% HS mineralization, while the rest of the HS were partially oxidized into low molecular weight compounds and building blocks. However, HS mineralization was limited with the MMO-anode. The mineralization and oxidation were accompanied by the formation of organic and inorganic chlorinated species. These species increased the toxicity to Vibrio fischeri 20-fold compared to the initially low-toxic CTBD. Thus, EO with a BDD-anode is a promising pre-treatment technology for the removal of OCs before CTBD deionization, but measures to minimize the chlorinated species formation are required before its application., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

Applying manganese(IV)- or iron(III)-(hydr)oxides to remove pharmaceuticals from water could be attractive, due to the capacity of these metal oxides to remove pharmaceuticals and be regenerated. As pharmaceutical removal under anaerobic conditions is foreseen, Mn(IV) or Fe(III) regeneration under anaerobic conditions, or with minimum oxygen dosage, is preferred. In this study, batch experiments are performed to investigate (1) Mn(IV) and Fe(III) regeneration from Mn(II) and Fe(II); (2) the pharmaceutical removal during biological Mn(IV) and Fe(III) regeneration; and (3) anaerobic abiotic pharmaceutical removal with different Mn(IV) or Fe(III) species. Results show that biological re-oxidation of reduced Mn(II) to Mn(IV) occurs under oxygen-limiting conditions. Biological re-oxidation of Fe(II) to Fe(III) is obtained with nitrate under anaerobic conditions. Both bio-regenerated Mn(IV)-oxides and Fe(III)-hydroxides are amorphous. The pharmaceutical removal is insignificant by Mn(II)- or Fe(II)-oxidizing bacteria during regeneration. Finally, pharmaceutical removal is investigated with various Mn(IV) and Fe(III) sources. Anaerobic abiotic removal using Mn(IV) produced from drinking water treatment plants results in 23% metoprolol and 44% propranolol removal, similar to chemically synthesized Mn(IV). In contrast, Fe(III) from drinking water treatment plants outperformed chemically or biologically synthesized Fe(III); Fe (III) from drinking water treatment can remove 31-43% of propranolol via anaerobic abiotic process. In addition, one of the Fe(III)-based sorbents tested, FerroSorp ® RW, can also remove propranolol (20-25%). Biological regeneration of Mn(IV) and Fe(III) from the reduced species Mn(II) and Fe(II) could be more effective in terms of cost and treatment efficiency., (Copyright © 2018 The Authors. Published by Elsevier Ltd.. All rights reserved.)