The impact of shipping emissions on ozone mixing ratio over Europe is assessed for July 2006 using the Community Multiscale Air Quality modeling system and the Netherlands Organization for Applied Scientific Research anthropogenic emission inventory. Results suggest that ship-induced ozone contribution to the total surface ozone exceeds 5% over the sea and near the coastline, while an increase up to 5% is simulated over a large portion of the European land. The largest impact (i.e., an increase up to 30%) is simulated over the Mediterranean Sea. In addition, shipping emissions are simulated to increase NO₂ mixing ratio more than 90%, locally, and to modify the oxidizing capacity of the atmosphere through hydroxyl radical formation (increase by 20–60% over the sea along the European coasts and near the coastal zone). Therefore, emissions from ships may counteract the benefits derived from the anthropogenic emissions reduction strategies over the continent. Simulations suggest regions where shipping emissions have a major impact on ozone mixing ratio compared to individual anthropogenic emission sector categories. Shipping emissions are estimated to play an important role on ozone levels compared to road transport sector near the coastal zone. The impact of shipping emissions on ozone formation is also profound over a great part of the European land compared to the rest of anthropogenic emission categories.

The treatment of winery effluents through sulphate radical-based advanced oxidation processes (SR-AOPs) driven by solar radiation is reported in this study. Photolytic and catalytic activations of peroxymonosulphate (PMS) and persulphate (KPS and SPS) at different pH values (4.5 and 7) were studied in the degradation of organic matter. Portugal is one of the largest wine producers in Europe. The wine making activities generate huge volume of effluents characterized by a variable volume and organic load, being their seasonal nature one of the most important drawbacks. Recently, SR-AOPs are gradually attracting attention as in situ chemical oxidation technologies, instead of hydroxyl radical AOPs (HR-AOPs). The studied concentrations are suitable to obtain notable values of organic matter degradation, with TOC removal around 50%. In general terms, no notable differences were observed between treatments at pH values 4.5 and 7. Photolytic activation of SPS with solar radiation treatments obtained the highest efficiency (28 and 40% of TOC removal with 1 and 50 mM, respectively, at pH 4.5) in comparison to KPS and PMS. The addition of a transition metal as catalyst, such as Fe(II) or Co(II), increased considerably the TOC removal efficiency higher than 50%, but not in all cases. For instance, the combination KPS or PMS with Co(II) at pH 4.5 did not allow to obtain better results than photolytic activation of these persulphate salts. In summary, the use of SR-AOPs could be a serious alternative as tertiary treatment for winery wastewaters.

The spatial distribution and seasonal variations of methylmercury (MeHg) in Wen-Rui-Tang (WRT) River network were investigated by monitoring the MeHg concentrations in surface water samples collected from 30 sites across the river network over four seasons. Detection frequencies and concentrations of MeHg were generally higher in January, indicating that low sunlight irradiation, wind speed, and temperature conditions might enhance the persistence of MeHg in surface water. The MeHg levels varied with sampling locations, with the highest concentrations being observed in the industrial area especially around wastewater outfall, revealing that the mercury contamination in WRT River mainly comes from the industrial wastewater. Photodegradation of MeHg in WRT River surface water and the effects of natural constituents such as fulvic acid (FA), ferric ions (Fe³⁺), nitrate (NO₃ ⁻), and dissolved oxygen on the MeHg photodegradation in aqueous solutions were studied under the simulated sunlight. The experimental data indicated that the indirect photodecomposition of MeHg occurred in WRT River surface water. Photodegradation of MeHg in FA solution was initiated by triplet ³FA* or MeHg-FA* via electron transfer interaction under light irradiations. The Fe³⁺ and NO₃ ⁻ can absorb light energy to produce ·OH and enhance the photochemical degradation of MeHg. The MeHg photodecompositions in FA, nitrate, and Fe³⁺ solutions were markedly accelerated after removing the dissolved oxygen.

TiO₂ hollow spheres and TiO₂ hollow spheres adorned with SnO₂ quantum dots were synthesized successfully under mild temperature and autogenous pressure using the hydrothermal route. X-ray diffraction, field emission scanning electron microscopy, scanning electron microscopy, transmission electron microscope, photoluminescence spectroscopy, and UV–vis spectroscopy were used to characterize the physical and chemical nature of the synthesized sample. The characterized samples were used in the photocatalytic applications to reduce the concentration of carbon dioxide in the presence of water under the influence of visible light. Our observation confirmed that with increasing SnO₂ content there is a tremendous change in the photocatalytic performance of the samples, due to free mobility of the electrons and holes and decline in charge recombination centers formed with the formation of nano-heterojunction between SnO₂ and TiO₂. The greater photocatalytic production of methanol was achieved using 2ST sample, i.e., 1.61 μmol/g/h which tends to decrease with an increase in SnO₂ content.

This study investigated changes over 25 years (1987–2012) in pesticide usage in orchards in England and Wales and associated changes to exposure and risk for resident pregnant women living 100 and 1000 m downwind of treated areas. A model was developed to estimate aggregated daily exposure to pesticides via inhaled vapour and indirect dermal contact with contaminated ground, whilst risk was expressed as a hazard quotient (HQ) based on estimated exposure and the no observed (adverse) effect level for reproductive and developmental effects. Results show the largest changes occurred between 1987 and 1996 with total pesticide usage reduced by ca. 25%, exposure per unit of pesticide applied slightly increased, and a reduction in risk per unit exposure by factors of 1.3 to 3. Thereafter, there were no consistent changes in use between 1996 and 2012, with an increase in number of applications to each crop balanced by a decrease in average application rate. Exposure per unit of pesticide applied decreased consistently over this period such that values in 2012 for this metric were 48–65% of those in 1987, and there were further smaller decreases in risk per unit exposure. All aggregated hazard quotients were two to three orders of magnitude smaller than one, despite the inherent simplifications of assuming co-occurrence of exposure to all pesticides and additivity of effects. Hazard quotients at 1000 m were 5 to 16 times smaller than those at 100 m. There were clear signals of the impact of regulatory intervention in improving the fate and hazard profiles of pesticides used in orchards in England and Wales over the period investigated.

It is confirmed that nano-ZnO (nZnO) has impact on environment and is considered as heavy metal pollutants. It is a new technology that applies coagulation process to simultaneous removal of the nanoparticles and heavy metals. Environmental chemical behavior of ZnO in water, such as the dispersion, aggregation, sedimentation, and dissolution of releasing metal ions, has been systematically studied in this paper. The result shows that three kinds of nZnO state such as compacted sediment, suspended, and released is separately 36.54 %, 40.61 %, and 22.86 %. Enteromorpha polysaccharide (Ep) was used together with polyaluminum chloride (PAC) in surface water purification. In order to study the mechanism of simultaneous removal of residual nZnO particles and Zn²⁺, coagulation process was further applied in this study. The evolution of flocs size, strength, and recovery ability and fractal structure due to Ep addition was systematically studied in this paper. Results indicated that PAC-Ep was efficient in removing nZnO and Zn²⁺, which leads to more than 95 % particles, 50–60 % natural organic matter (NOM) removed, and 35 % of resolved heavy metal ion adsorbing-chelation. Ep was an efficient coagulant aid in enhancing performance of coagulation and generating flocs with bigger sizes, faster growth rates, and higher recovery abilities. Additionally, the flocs formed by PAC-Ep presented a much looser structure than flocs formed only by PAC. Graphical abstract ᅟ

Thermal treatment of polychlorinated biphenyls (PCB) contaminated soil was shown in earlier work to generate polychlorinated dibenzo-p-dioxins (PCDD) and polychlorinated dibenzofurans (PCDF). In this study, the PCDD/F were studied arising during the remediation of p,p′-DDT contaminated soil by thermal desorption. Three kinds of soil (sandy, clayey and lateritic soil) were tested to investigate the effect of soil texture on PCDD/F formation. Those soils were artificially polluted with p,p′-DDT, obtaining a concentration level of 100 mg/kg. Thermal desorption experiments were conducted for 10 min at 300 °C in an air atmosphere. The total concentration of PCDD/F generated for three soils were 331, 803 and 865 ng/kg, respectively, and TeCDD and TeCDF were dominant among all PCDD/F congeners. After thermal desorption, the total amount of PCDD/F generated both in soil and in off-gas correlated positively with the amount of DDT added to soil. In addition, a possible pathway of the formation of PCDD/F was presented.

Miyun Reservoir is one of the most important drinking water sources for Beijing. Thirteen atmospheric PM sampling sites were established around this reservoir to analyze the mineral composition, morphological characteristics, element concentration, and sources of atmospheric PM pollution, using transmission electron microscope, X-ray diffraction, and inductively coupled plasma mass spectrometry analyses. The average monthly dry deposition flux of aerosols was 15.18 g/m², with a range of 5.78–47.56 g/m². The maximum flux season was winter, followed by summer, autumn, and spring. Zn and Pb pollution in this area was serious, and some of the sample sites had Cr, Co, Ni, and Cu pollution. Deposition fluxes of Zn/Pb in winter and summer reached 99.77/143.63 and 17.04/33.23 g/(hm² month), respectively. Principal component analysis showed two main components in the dry deposition; the first was Cr, Co, Ni, Cu, and Zn, and the other was Pb and Cd. Principal sources of the trace elements were iron mining and other anthropogenic activities in the surrounding areas and mountainous area north of the reservoir. Mineralogy analysis and microscopic conformation results showed many iron minerals and some unweathered minerals in dry deposition and atmospheric particulate matter, which came from an iron ore yard in the northern mountainous area of Miyun County. There was possible iron-rich dry deposition into Miyun Reservoir, affecting its water quality and harming the health of people living in areas around the reservoir and Beijing.

Seasonal effects of pre-aeration on microbial nitrogen performance in constructed wetlands (CWs) involved with anaerobic ammonium oxidation (anammox) process were investigated in this study. Slow natural re-aeration rate was the inhibiting factor for total nitrogen removal in CW without pre-aeration, and partial nitrification was the main way for nitrite generation. Besides partial nitrification, pre-aeration provided nitrite generation in CWs with an alternative way: nitrate reduction. Advantage of pre-aeration of influent was much different under various temperature ranges. Mean temperature of 15 °C seemed to be the turning point. With a mean temperature of or higher than 15 °C, nitrate in the influent effectively improved nitrogen removal in CWs. With a mean temperature lower than 15 °C, the nitrate reduction process in CWs was greatly inhibited. The benefit of pre-aeration was weak under this temperature range. Seasonal aeration pattern for the pre-treatment of HSSF CWs might be a more energy-saving alternative in in-suit domestic sewage treatment.

This paper explored biochar modification to enhance biochar’s ability to adsorb hexavalent chromium from aqueous solution. The ramie stem biomass was pyrolyzed and then treated by β-cyclodextrin/poly(L-glutamic acid) which contained plentiful functional groups. The pristine and modified biochar were characterized by FTIR, X-ray photoelectron spectroscopy, specific surface area, and zeta potential measurement. Results indicated that the β-cyclodextrin/poly(L-glutamic acid) was successfully bound to the biochar surface. Batch experiments were conducted to investigate the kinetics, isotherm, thermodynamics, and adsorption/desorption of Cr(VI). Adsorption capacities of CGA-biochar were significantly higher than that of the untreated biochar, and its maximum adsorption capacity could reach up to 197.21 mg/g at pH 2.0. Results also illustrated that sorption performance depended on initial solution pH; in addition, acidic condition was beneficial to the Cr(VI) uptake. Furthermore, the Cr(VI) uptake was significantly affected by the ion strength and cation species. This study demonstrated that CGA-biochar could be a potential adsorbent for Cr(VI) pollution control.