Identification and removal of polycyclic aromatic hydrocarbons (PAHs) were investigated at two coke plants located in Shaoguan, Guangdong Province of China. Samples of raw coking wastewaters and wastewaters from subunits of a coke production plant were analyzed using gas chromatography-mass spectrometry (GC/MS) to provide a detailed chemical characterization of PAHs. The identification and characterization of PAH isomers was based on a positive match of mass spectral data of sample peaks with those for PAH isomers in mass spectra databases with electron impact ionization mass spectra and retention times of internal reference compounds. In total, 270 PAH compounds including numerous nitrogen, oxygen, and sulfur heteroatomic derivatives were positively identified for the first time. Quantitative analysis of target PAHs revealed that total PAH concentrations in coking wastewaters were in the range of 98.5 ± 8.9 to 216 ± 20.2 μg/L, with 3-4-ring PAHs as dominant compounds. Calculation of daily PAH output from four plant subunits indicated that PAHs in the coking wastewater came mainly from ammonia stripping wastewater. Coking wastewater treatment processes played an important role in removing PAHs in coking wastewater, successfully removing 92 % of the target compounds. However, 69 weakly polar compounds, including PAH isomers, were still discharged in the final effluent, producing 8.8 ± 2.7 to 31.9 ± 6.8 g/day of PAHs with potential toxicity to environmental waters. The study of coking wastewater herein proposed can be used to better predict improvement of coke production facilities and treatment conditions according to the identification and removal of PAHs in the coke plant as well as to assess risks associated with continuous discharge of these contaminants to receiving waters.

The spatial distribution of persistent organic pollutants (POPs) was examined in soils surrounding the Tanggu Chemical Industrial District in Tianjin, China. The concentrations of hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs), hexachlorobenzenes (HCBs), and polychlorinated biphenyls (PCBs) were determined in 70 surface soils using accelerated solvent extraction and gas chromatography with electron capture detection. The results showed that the ranges of ∑HCH, ∑DDT, ΣHCB, and ∑PCB concentrations in soils were 2.1–12,549 μg kg⁻¹ (average, 965 μg kg⁻¹), n.d.–2,033 μg kg⁻¹ (average, 88.4 μg kg⁻¹), n.d.–1,924 μg kg⁻¹ (average, 349 μg kg⁻¹), and n.d.–373 μg kg⁻¹ (average, 46.2 μg kg⁻¹), respectively. Of these, HCHs were the dominant POPs, accounting for 75 % of the total organochlorine pesticide (OCP) residues. Overall, the spatial distribution of OCP concentrations showed a decreasing trend from the center of the Tanggu District to the surrounding areas. Two major pollution sources were Tianjin Dagu Chemical Co., Ltd. in the district center and the Tianjin Chemical Plant in Hangu District. In contrast, PCB concentrations were relatively high in the Haihe estuary to the east and low to the west of the study area. Component analysis of OCPs in these soils showed that they mainly came from industrial point sources. Compared with soils in other regions, soil DDT pollution was at a medium level in the Tanggu Chemical Industrial District, but associated HCH, HCB, and PCB pollution was relatively heavy. By multivariate statistical analyses, Tianjin Dagu Chemical Co., Ltd. was recognized as the main source of POPs, and soil properties were clarified to play an important role on the distribution and composition of POPs, especially the organic carbon content.

Many best management practices have been developed and implemented to treat the nonpoint source pollution of the aquatic environment in Korea's four major river basins. The performance and cost of these facilities were evaluated and compared using broad categories, including grassed swales, constructed wetlands, vegetated filter strips, hydrodynamic separators, media filters, and infiltration trenches, based on the monitoring and maintenance work undertaken between 2005 and 2012. Constructed wetlands, media filters, and infiltration trenches generally performed better in removing pollutants than other types of facilities, while media filters were the most expensive factor in terms of construction and operational costs. In addition, constructed wetlands incurred the least operational cost, as well as helping to control the quantity of runoff. This illustrates that a high cost facility does not necessarily give a better performance. A slightly more expensive facility, such as wetland, could prove to be a reasonably effective treatment. The selection of the most appropriate treatment for stormwater runoff should be based on an overall analysis of performance and cost.

Drinking water treatment residuals (WTRs), nonhazardous by-products generated in a drinking water treatment plant, can be reused to immobilize phosphorus (P) to control the internal P loading from lake sediments for eutrophication control. Reasonably, before practical application, it is essential to determine the P immobilization capability of WTRs in lake sediments under various conditions. In this work, laboratory scale experiments were conducted to investigate the effects of light, microbial activity, and sediment resuspension on the P immobilization capability of WTRs. The results suggested that absence of light, low microbial activity, and sediment resuspension can increase the internal P loading from lake sediments. WTRs can, however, reduce the internal P loading significantly. Further analysis demonstrated that WTRs can stabilize P, decreasing the P bioavailability in the sediments under varied conditions. WTRs also presented little undesirable effects on the dissolved oxygen levels and pH of overlying water. Therefore, light, microbial activity, and sediment resuspension have little effect on the P immobilization capability of WTRs in lake sediments.

Long-term mining and smelting activities brought a series of environmental issues into soils in Wanshan mercury (Hg) mining area (WMMA), Guizhou, China. Several studies have been published on the concentrations of Hg in local soils, but a comprehensive assessment of the mass of Hg in soil induced by anthropogenic activities, as presented in this paper, has not been previously conducted. Three districts of WMMA were chosen as the study areas. We summarized previous published data and sampled 14 typical soil profiles to analyze the spatial and vertical distributions of Hg in soil in the study areas. The regional geologic background, direct and indirect Hg deposition, and Hg-polluted irrigation water were considered as the main sources of Hg contaminations in local soils. Furthermore, the enrichment factor (EF) method was applied to assess the extent of anthropogenic input of Hg to soil. Titanium (Ti) was chosen to be the reference element to calculate the EF. Generally, the elevated values of EF were observed in the upper soil layers and close to mine wastes. The total budget of Hg in soil contributed from anthropogenic sources was estimated to be 1,227 t in arable soil and 75 t in natural soil. Our data showed that arable soil was the major sink of anthropogenic Hg in the study area.

A microarray for the detection of toxic algal species was developed in the European Union 7th Framework project MIDTAL. We initially tested all available fluorescence in situ hybridisation probes for toxic algae, which are normally designed to a length of 18 nt, and found that in most cases the signal was rather weak or all probes designed from the second half of the molecule were inaccessible in a microarray format because of secondary structure of the ribosomal RNA molecule We modified the length of the probes, the fragmentation of the rRNA, the stringency of the washing buffers and the length of the spacer molecules linking the probes to the glass surface of the microarray. Because of the secondary structure of the rRNA molecule, regions of the molecule can be difficult to access by the probes. Each of these modifications has improved probe accessibility and probe specificity to reduce false positives.

The electrochemical abatement of the drug ibuprofen (2-(4-isobutylphenyl)propionic acid) from aqueous solution has been carried out by anodic oxidation. The electrolyses have been performed at constant current using a small, undivided cell equipped with a Pt or thin-film boron-doped diamond (BDD) anode and a carbon-felt cathode. The results have shown that ibuprofen has been destroyed under all the conditions tested, following pseudo-first-order kinetics; however, BDD enables higher removal rates than Pt, because the former produces greater quantity of •OH. Using BDD anode, the pseudo-first-order rate constant increased with applied current and when NaCl replaced Na₂SO₄ as supporting electrolyte, while it is almost unaffected by ibuprofen concentration. Mineralization of ibuprofen aqueous solutions was followed by total organic carbon (TOC) measurements. After 8 h of electrolysis, TOC removal varied from 91 % to 96 % applying a current in the range of 50–500 mA. The reaction by-products were quantified by chromatographic techniques, and in particular, aliphatic acids (oxalic, glyoxylic, formic, acetic, and pyruvic) have been the main intermediates formed during the electrolyses. The absolute rate constant for the oxidative degradation of ibuprofen have also been determined, by competition kinetic method, as 6.41 × 10⁹ M⁻¹ s⁻¹.

The aim of the present research is to develop economic, fast, and versatile method for the removal of toxic organic pollutant phenol from wastewater using eggshell. The batch experiments are conducted to evaluate the effect of pH, phenol concentration, dosage of adsorbent, and contact time on the removal of phenol. The paper includes in-depth kinetic studies of the ongoing adsorption process. Attempts have also been made to verify Langmuir and Freundlich adsorption isotherms. The morphology and characteristics of eggshell have also been studied using scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and X-ray fluorescence analysis. At ambient temperature, the maximum adsorption of phenol onto eggshells has been achieved at pH 9 and the contact time, 90 min. The experimental data give best-fitted straight lines for pseudo-first-order as well as pseudo-second-order kinetic models. Furthermore, the adsorption process verifies Freundlich and Langmuir adsorption isotherms, and on the basis of mathematical expressions of these models, various necessary adsorption constants have been calculated. Using adsorption data, various thermodynamic parameters like change in enthalpy (∆H (0)), change in entropy (∆S (0)), and change in free energy ∆G (0) have also been evaluated. Results clearly reveal that the solid waste material eggshell acts as an effective adsorbent for the removal of phenol from aqueous solutions.

Surveys on pre- and post-impoundment total mercury concentrations in water, seston and fish were conducted during 2007-2008 in the Wujiang River, southwest China. Compared with the pre-impoundment, total mercury in the reservoir and downstream water rapidly increased by 164-303 % during the first half year of flooding, and then decreased by 61.7-62.2 % after 9 months of flooding. However, total mercury in seston from the reservoir and downstream generally declined. There was no significant difference in the total mercury between reservoir fish with different habitat preference and feeding habit. We find that fish tissue mercury concentration significantly increased threefold after flooding, and the increasing rate is lower than those in subarctic and temperate reservoirs. The pre- and post-impoundment fish samples exceeding the Chinese hygienic standard for tolerances of mercury in foods increased from 1.3 to 17.4 %. Long-term monitoring of fish mercury level in Wujiang River should be undertaken to ensure local food security.

Living in an area chronically polluted with metals is usually associated with changes in the energy distribution in organisms due to increased energy expenses associated with detoxification and excretion processes. These expenses may be reflected in the available energy resources, such as lipids, carbohydrates, and proteins. In this context, the energy status of Pterostichus oblongopunctatus (Coleoptera: Carabidae) was studied in two metal pollution gradients near Olkusz and Miateczko Śląskie in southern Poland. Both regions are rich in metal ores, and the two largest Polish zinc smelters have been operating there since the 1970s. Beetles were collected from five sites at each gradient. Zinc and cadmium concentrations were measured in both the soil and the beetles. The possible reduction in energy reserves as a cost of detoxifying assimilated metals was evaluated biochemically by determining the total lipid, carbohydrates, and protein contents. At the most polluted sites, the Zn concentration in the soil organic layer reached 2,906 mg/kg, and the Cd concentration reached 55 mg/kg. Body Zn and Cd concentrations increased with increasing soil Zn and Cd concentrations (p = 0.003 and p = 0.0001, respectively). However, no relationship between pollution level and energetic reserves was found. The results suggest that populations of P. oblongopunctatus inhabiting highly metal-polluted sites are able to survive without any serious impact on their energy reserves, though they obviously have to cope with elevated body metal concentrations.