Treatment of Polysilicon Production Wastewater by Ferrate(VI) Microcapsule Oxidation and Biological Aerated Biofilter Abstract Polysilicon production wastewater (PPW) is characterized by complex composition, high chemical oxygen demand (COD) concentration and poor biodegradability. An integrated process comprising of ferrate(VI) oxidation and biological aerated biofilter (BAF) was developed at lab scale for treating PPW with an initial COD of 3630 mg/L, biochemical oxygen demand (BOD5) of 350 mg/L, suspended solids (SS) of 440 mg/L, and turbidity of 430 nephelometric turbidity units (NTU). Firstly, the potassium ferrate(VI) (K2FeO4) microcapsules were synthesized by using the phase separation method in cyclohexane, and ethylcellulose was used as the microcapsule wall materials (WM). The stability could be enhanced greatly when ferrate(VI) was encapsulated in the microcapsules with a mass ratio of K2FeO4:WM of 1:4 in the air compared with pure K2FeO4. The microcapsules exhibited sustained release behaviour and higher oxidation efficiency than pure K2FeO4. The microcapsules were used to pretreat PPW. Under the oxidation conditions of pH 6.0, microcapsule dosage 5.0 g/L and reaction time 70 min, the removal efficiency of COD, suspended solids (SS) and turbidity reached 55.1%, 61.3% and 74.2%, respectively. Subsequently, the oxidation effluent was subjected to BAF treatment. Under a hydraulic residence time of 48 h and a gas:water ratio of 6:1, the final effluent values of COD, SS and turbidity were 308 mg/L, 35 mg/L and 28 NTU, respectively, corresponding to total removal of 91.5%, 92.0% and 93.5%, respectively. Thus, this work demonstrates the feasible and potential application of encapsulated ferrate(VI) samples in the degradation of various toxic effluents.

Free Amino Acid Accumulation in Soil and Tomato Plants ( Solanum lycopersicum L.) Associated with Arsenic Stress Abstract Pollution of soils with arsenic leads to changes in biochemical processes both in the soil and in plants growing on it. Biochemically active compounds, such as free amino acids, strongly respond to the increase of the content of toxic substances in the environment. This article deals with the changes in the concentration of free amino acids in soil, roots, and aboveground biomass of tomato plants that took place when soil was contaminated with arsenic. Pre-grown tomato plants (Solanum lycopersicum L.) were transplanted into containers with soil contaminated with arsenate (As(V)) at the doses of 50 and 200 mg kg−1. In the soils, roots, and aboveground parts of plants, the changes in the concentration of 16–17 free amino acids were studied by the method of high-performance liquid chromatography. The results of the experiment showed that soil contamination with arsenic can lead to an increase in the concentration of all studied amino acids, both in soils and in tomato plants. Total free amino acid concentration in soil increased by 194.2% at 50 mg kg−1 of As(V) and by 349.6% at 200 mg kg−1 of As(V), in roots and aboveground biomass their concentration increased from 1.5 to 4.6 times. A particularly strong increase of concentration in soil was observed for serine and glycine, whereas in plant tissues, in comparison with other amino acids, aspartic and glutamic acids were intensively accumulated. The strong correlation between the content of free amino acids in the soils and in the roots (r = 0.85) or aboveground biomass of plants (r = 0.88) shows that both soil and tomato plants respond to soil contamination with As(V) in a similar way. However, the results of the study also showed that increasing of amino acid concentration in plant tissues in case of arsenic contamination can be associated with both their accumulations due to the plant’s response to stressful conditions and probably their uptake from the soil.

Decomposition of 2-Propanol in the Liquid Phase Using a Photocatalyst Immobilized on Nonwoven Fabric and Ozone Microbubbles Abstract 2-Propanol (IPA) is a highly water-soluble volatile organic compound that is used in the cleaning and drying processes during semiconductor fabrication. IPA is also used as a disinfectant in the pharmacy field. Water scrubber processing is one of the methods used for IPA collection. However, water scrubbing requires wastewater treatment. In this study, we propose a decomposition system for IPA in the liquid phase based on a TiO2 photocatalyst immobilized on nonwoven fabric (TiO2 nonwoven fabric) and ozone microbubbles (MBs). The thick nonwoven fabric with immobilized TiO2 exhibits a higher IPA removal rate than that exhibited by the pleated fabric. IPA decomposes to produce acetone, which can be further decomposed and possibly undergo mineralization. The entire water tank can be supplied with ozone by introducing the MB-forming ozone, which considerably affects the decomposition of IPA. The efficient decomposition of IPA was achieved by combining ozone MBs, TiO2 nonwoven fabric, and ultraviolet irradiation, presumably because the photocatalyst promotes the mineralization of the decomposition product. Thus, the OH radicals from the O3 MBs competitively captured in the decomposition product strongly promote the decomposition of IPA, enhancing the IPA decomposition rate.

Effects of Temperature on the Transport of Suspended Particles Through Sand Layer During Groundwater Recharge Abstract This paper presents an experimental study of suspended particle transport through sand layer using a new self-developed sand layer transportation-deposition testing system, and the study aims to identify the effects of temperature on the transport of suspended particles through porous medium. Four typical temperatures (5 °C, 15 °C, 25 °C, and 35 °C) were considered in our study, and the experiments were conducted under four size compositions and three flow velocities (1.5 cm/s, 0.2 cm/s, and 0.04 cm/s). The tests were conducted using quartz sand as the porous medium and quartz powder as particles to monitor the change in turbidity under the different conditions. The breakthrough curves were analyzed, and the results demonstrated that changes in temperature can affect the breakthrough curves, especially at the peak. The influence is particularly significant under lower flow velocities and for smaller particles. In regard to the influence factors on the transport process, water viscosity and adsorption effect can be regarded as promoting factors, while kinetic energy of particles can be classified as constraining factors.

A Comparative Adsorption Study with Various Adsorbents for the Removal of Ciprofloxacin Hydrochloride from Water Abstract In this study, the removal of ciprofloxacin hydrochloride (a fluoroquinolone antibiotic) by using various effective adsorbents such as activated carbon, montmorillonite, modified montmorillonite (commercial name Cloisite 20A), and alumina was investigated. Adsorption experiments were performed to determine and compare the adsorption capacities of these adsorbents. The adsorption capacities of adsorbents were examined at different initial concentrations of ciprofloxacin hydrochloride. Activated carbon was found to be having the best adsorption capacity for the removal of ciprofloxacin hydrochloride. For the solution having an initial ciprofloxacin hydrochloride concentration of 4 ppm, the adsorption capacities of adsorbents were obtained as 1.86 mg g−1 for activated carbon, 1.67 mg g−1 for modified montmorillonite, 1.15 mg g−1 for alumina, and 0.60 mg g−1 for montmorillonite. And also, about 92% of the ciprofloxacin hydrochloride was removed from the water using the activated carbon. In addition, Langmuir, Freundlich, and Temkin isotherm models were employed to express the adsorption process. For all adsorbents, Freundlich isotherm model provided best fitting to the experimental data because of very high values of R2 (> 0.99). Kinetic models of pseudo-first order, pseudo-second order, Elovich, and Weber-Morris intraparticle diffusion model were utilized to evaluate the experimental adsorption data. Adsorption kinetics data were well represented by pseudo-second order kinetic model with values of R2 (> 0.999).

Rapid Analysis of Polycyclic Aromatic Hydrocarbons in Water Samples Using an Automated On-line Two-Dimensional Liquid Chromatography Abstract Two-dimensional HPLC (2D-HPLC) recently has received great attention due to providing high resolving power and higher peak capacities than that of 1D-HPLC, especially dealing with a wide spectrum of sample matrices containing several components. In this work, an on-line heart-cutting two-dimensional liquid chromatography (2D-LC) method was developed using monolithic columns coupled with reversed-phase liquid chromatography (RPLC). 2D-HPLC was successfully carried out using affinity-based monolithic columns at first dimension (20 cm × 4.6 mm I.D.) followed by a Pinnacle II PAH column (50 mm × 4.6 mm I.D.) at the second dimension. Furthermore, good linearity was observed for the correlation of the benzo[a]pyrene (BaP) molecule against the peak areas (R2 = 0.994) in the concentration range of 0.01–1.0 ng/mL in 30 min. The limit of detection and the limit of quantification were found to be 4.0 pg/mL and 12.0 pg/mL, respectively. Both the intra-day and inter-day precision at 0.01 and 0.1 ng/mL spiked concentrations were below than 2.35% RSD whereas the means of the recovery data of the BaP from the water samples were found to be in the range of 93.71–98.65%. These results demonstrate that the 2D-HPLC system, developed by the combination of the P(HEMA-MAPA) column and Pinnacle II PAH column, is reliable, stable, and well qualified in the extraction of polycyclic aromatic hydrocarbons from the water samples.

Cerium Oxide Nanoparticles Affect Heavy Metals Uptake by Pea in a Divergent Way than Their Ionic and Bulk Counterparts Abstract The impact of cerium oxide nanoparticles, bulk cerium oxide and ionic cerium nitrate on the plant development as well as the uptake and further translocation of Cu, Mn, Zn and Fe by sugar pea (Pisum sativum L.) was investigated. Plants were cultivated in the laboratory pot experiments using the modified Hoagland solutions supplemented with cerium compounds at the 200 mg L−1 Ce level. Analysis of variance proved that cerium oxide nanoparticles significantly decreased Cu, Mn, Zn and Fe concentrations in roots and above ground parts of the pea plants. The latter ions are presumably transported via symplastic pathways and may compete with nanoparticles for similar carriers. The lowest impact on the plant growth and the metal uptake was observed under the bulk CeO2 treatment. On the contrary, strongest interactions were observed for supplementation with ionic cerium nitrate. The highly beneficial effect of cerium oxide nanoparticles on the plant growth was not supported by this study. The latter conclusion is of particular relevance when environmental impact of cerium compounds on the waste management, municipal urban low emissions and food production is to be concerned.

Fungal and Bacterial Co-Bioaugmentation of a Pesticide-Degrading Biomixture: Pesticide Removal and Community Structure Variations during Different Treatments Abstract Biopurification systems (BPS) are employed for the treatment of pesticide-containing wastewaters. In this work, a biomixture (active core of BPS) complemented by the addition of the fungus Trametes versicolor was evaluated for the elimination of a mixture of pesticides under different treatment conditions. The biomixture achieved high removal of all the pesticides assayed after 16 d: atrazine (68.4%, t1/2: 9.6 d), carbendazim (96.7%, t1/2: 3.6 d), carbofuran (98.7%, t1/2: 3.1 d) and metalaxyl (96.7%, t1/2: 3.8 d). Variations in the treatment conditions including addition of the antibiotic oxytetracycline and co-bioaugmentation with a bacterial consortium did not significantly affect the removal performance of the biomixture. Bacterial and fungal community profiles determined by DGGE analyses revealed changes that responded to biomixture aging, and not to antibiotic or pesticide addition. The proposed biomixture exhibits very efficient elimination during simultaneous pesticide application; moreover, the matrix is highly stable during stressful conditions such as the co-application of antibiotics of agricultural use.

Four Decades of Organic Anthropogenic Pollution: a Compilation for Djerdap Lake Sediments, Serbia Abstract Analysis of limnic sediments can serve as a tool to assess sedimentary pollution for both the status quo as well as changes over time. However, in environmental studies, often only a small number of established well-studied contaminants are considered. This study focused on a more comprehensive investigation of sedimentary pollution of Djerdap Reservoir. Therefore, complementary analytical approaches were applied covering lipophilic organic contaminants and heavy metals. Investigations were performed on limnic sediment layers representing a period of 43 years of reservoir functioning. The core was sectioned on 11 samples and analyzed for, loss on ignition (LOI), and organic compounds (gas chromatography-mass spectrometry). Here, we report the quantitative data of 43 lipophilic organic compounds indicating both domestic and industrial emissions. Measured concentrations are generally low. Surprisingly, no polychlorinated biphenyls have been detected. Data concerning grain size, sedimentological, and inorganic composition were measured and published by in Kasanin-Grubin et al. (Kasanin-Grubin et al. 2019).

Effects of Antibiotics on Microbial Communities Responsible for Perchlorate Degradation Abstract Perchlorate, a pervasive water pollutant, poses a threat to some aquatic environments. Antibiotics, as an emerging contaminant, have increasingly been found in aquatic environments in recent years. As a special co-contaminant, antibiotics modify the composition and function of microbial communities, and the biodegradation rate of perchlorate is changed in the environment. In this study, three typical antibiotics widely found in aquatic ecosystems (lincomycin (LIN), erythromycin (ETM), and sulfadiazine (SDZ)) and two input modes (once and multiple times) were selected to reveal the effects of antibiotics on perchlorate degradation and changes in the microbial community. Additionally, antibiotic resistance gene (ARG) abundance and microbial community composition were analyzed to illustrate the response of bacteria to antibiotic types and input methods by QPCR and high-throughput sequencing. The perchlorate degradation rate was inhibited by three antibiotics (LIN > ETM > SDZ) in this study. LIN and ETM had stronger inhibitory effects on perchlorate degradation, and the abundances of their ARGs increased with increasing antibiotic concentrations. With the continuous culturing and multiple inputs of antibiotics, the percentage of ARGs decreased after crossing a threshold. Additionally, the dominant degradation bacteria were different under pressure from different antibiotics. The type of the antibiotic, the background level of ARGs, and the dissemination of ARGs between bacteria were the main factors influencing the degradation system. The results presented herein will help us understand the modifications of microbial communities that occur in persistent pollutant systems contaminated with antibiotics.