Herbaspirillum chlorophenolicum strain FA1, a gram-negative bacterium isolated from activated sludge, was found to be able to use pyrene as sole carbon and energy sources. During biodegradation, the contribution of biosorption to the whole pyrene removal mattered in the early reaction stage, and biodegradation was the predominant process. Pyrene biodegradation was significantly enhanced with the presence of a typical carboxylated aromatic metabolite (phthalic acid) at concentrations of 30–50 mg l⁻¹, and the metabolite itself could also be efficiently biodegraded. For the purpose of practical application, immobilization of strain FA1 was carried out, and polyvinyl alcohol (PVA)-diatomite carrier by chemical method was proved to be the most efficient, with a PYR biodegradation of 92.8 % in 10 days. Investigation on the pyrene biodegradation kinetics by both free and immobilized cells showed that the experimental data fitted well to the first-order kinetic model. Besides, the PVA-diatomite carrier (chemical method) could be reused in at least eight consecutive biodegradation processes of PYR without any significant decrease in biodegradation efficiency. Further storage stability tests revealed that the ability to degrade pyrene using immobilized cells remained stable after storage at 4 °C for 45 days. Moreover, strain FA1 exhibited a relative broad substrate profile, including naphthalene, fluorene, phenanthrene, anthracene, fluoranthene, benzo[b]fluoranthene, benzene, toluene, and Tween 80. Taken together, results indicate that strain FA1 might be high potential in the development of treatment technologies for PAHs contamination.

Tropical forests play an important role in carbon cycle. However, the temporal and spatial variation in soil carbon dioxide (CO₂) emission of tropical forest remains uncertain, especially near the Tropic of Cancer. In this research, we studied the annual soil CO₂ fluxes from three tropical montane rainforests on the Hainan Island of China (pristine montane rainforest, PF; secondary montane rainforest, SF; and Podocarpus imbricatus plantation, PP). The results showed a lower annual average soil CO₂ flux as 6.85 ± 0.52 Mg C-CO₂ ha⁻¹ (9.17 Mg C-CO₂ ha⁻¹ in the wet season and 4.50 Mg C-CO₂ ha⁻¹ in the dry season). The CO₂ fluxes exhibited obviously seasonal variation during the study period. Among the three forest types, PF had the highest average CO₂ flux rate of 317.77 ± 147.71 mg CO₂ m⁻² h⁻¹ (433.08 mg CO₂ m⁻² h⁻¹ in the wet season and 202.47 mg CO₂ m⁻² h⁻¹ in the dry season), followed by PP of 286.84 ± 137.48 mg CO₂ m⁻² h⁻¹ (367.12 mg CO₂ m⁻² h⁻¹ in the wet season and 206.56 mg CO₂ m⁻² h⁻¹ in the dry season) and SF of 255.09 ± 155.26 mg CO₂ m⁻² h⁻¹ (351.48 mg CO₂ m⁻² h⁻¹ in the wet season and 155.71 mg CO₂ m⁻² h⁻¹ in the dry season). We found between CO₂ fluxes and soil temperature a highly significant linear relation (P < 0.01) at 5 cm depth and a highly significant exponential correlation (P < 0.01) at 10 cm depth for all three forest types; a significant linear relation (P < 0.05) between CO₂ fluxes and soil moisture content was found for SF and PF, but not for PP (P > 0.05). The CO₂ flux was significantly correlated (P < 0.05) with water-filled pore space only for PF. In conclusion, our results suggested soil CO₂ fluxes in the three forest types that exhibit obviously spatial and temporal variation, and the temperature is the major factor affecting soil CO₂ fluxes from this region.

TiO₂-graphene (TiO₂-GR) composites were successfully prepared by a two-step solvothermal method using titanium dioxide and natural graphite powder. X-ray diffraction (XRD) patterns showed that graphene oxide (GO) was prepared from natural flake graphite by a modified hydrothermal pressurized oxidation method. The results of Fourier transform infrared spectroscopy (FTIR) proved that TiO₂-GR composites were synthesized during the process of hydrothermal reaction while GO was changed into graphene. X-ray photoelectron spectroscopy (XPS) demonstrated that TiO₂ particles contacted closely with graphene via Ti–O–C bonds. The results of Raman spectra confirmed the existence of graphene in the TiO₂-GR composite. Scanning electron microscopy (SEM) images showed that TiO₂ particles were oval and grafted on the graphene sheet which was smooth with ripples. UV-visible diffuse reflectance spectra demonstrated that there was a red shift in the absorption edge of TiO₂-GR composite. The experimental results indicated that the TiO₂-GR composite had significantly adsorption-photocatalytic activity for the degradation of methylene blue (MB) dyes. The adsorption capacity (q ₘₐₓ) of TiO₂-6%GR-4h for MB was 41.32 mg ⋅ g⁻ ¹ calculated based on the Langmuir adsorption model, which was about 3.3 times the adsorption capacity of TiO₂. Adsorption kinetics studies showed that the adsorption process fit well with the pseudo-second-order model. It proved that the TiO₂-GR composites were more efficient than the pure TiO₂ in the field of environmental protection.

Due to natural and production activities, mercury contamination has become one of the major environmental problems over the world. Mercury contamination is a serious threat to human health. Among the existing technologies available for mercury pollution control, the adsorption process can get excellent separation effects and has been further studied. This review is attempted to cover a wide range of adsorbents that were developed for the removal of mercury from the year 2011. Various adsorbents, including the latest adsorbents, are presented along with highlighting and discussing the key advancements on their preparation, modification technologies, and strategies. By comparing their adsorption capacities, it is evident from the literature survey that some adsorbents have shown excellent potential for the removal of mercury. However, there is still a need to develop novel, efficient adsorbents with low cost, high stability, and easy production and manufacture for practical utility.

This is a green method for determination of mercury ion (Hg²⁺) in environmental samples. The method of exchangeable water based on liquid-liquid microextraction (EW-LLME) was first time introduced as a green analytical separation technique. Exchangeable water was made by the reaction of carbon dioxide with diethylenetriamine. The exchanging phenomena from low polarity to high polarity were confirmed by Fourier transforms infrared spectrometry. The complex formation between Hg²⁺ and 1, 5-diphenylcarbazone was achieved under the optimized experimental conditions. The enrichment factor and limits of detection of the present method were obtained to be 45.2 and 0.5 ng L⁻¹, respectively. The accuracy of the present method was confirmed with certified reference materials. The EW-LLME was successfully applied for determination of Hg²⁺ in solid matrices of block-III and V of Thar coalfield.

The reduction of nitrous oxide (N₂O) emission during nitrogen removal process in municipal wastewater treatment is of great urgency. Sequencing batch biofilm reactor (SBBR) system could be a promising and efficient way to solve the problem. In order to get the high chemical oxygen demand (COD) and nitrogen removal efficiency and low nitrous oxide emission, the influence of biofilm density on SBBR was investigated. When the biofilm density changed from 15 to 30 %, the effluent COD, total nitrogen (TN) and ammonia nitrogen decreased, but the effluent TN concentration did not meet the class I-B standard of the Discharge Standard of Pollutants for Municipal Wastewater Treatment Plant in China. COD, TN, and ammonia nitrogen concentration was 42.34, 19.14 and 2.97 mg/L at 50 % biofilm density. When the density turned from 50 to 70 %, although the effluent COD, TN, and ammonia nitrogen were still decreased, N₂O emission increased from 0.45 to 0.77 %. Considering the effluent quality and N₂O emission, the optimal biofilm density in SBBR was 50 %.

Phosphorus (P) loss from diffuse sources remains as the main cause of freshwater eutrophication in agricultural regions. The amount of land used for different agricultural practices may be a strong explanatory factor for the P loading to runoff waters. A prerequisite is that the effect of changes in land use on P levels in surface waters needs to be ascertained and quantified. In this study, a comprehensive approach has been developed to explore the environmental consequences of P levels in receiving water with corresponding land use change in a heavily agriculturally influenced watershed. A coupled simulation using Dyna-CLUE model with grey relational analysis (GRA) and grey model GM (1,1) model was employed to stimulate spatial distribution and area demand. Besides, a comprehensive land use index with degree of P saturation (DPS%) as weight coefficient was developed to examine the statistical and spatial relationships of land use and P levels in receiving waters on regional watershed. Moreover, in order to evaluate the practical impact of land use change on water quality, a planned emigration and watershed ecological reconstruction planning were designed into the scenarios. The potential of changes in land use as an abatement action to curb eutrophication was evaluated by modelling the effect of issued emigration and ecological restoration programs in the local watershed of the Yuqiao water reservoir in northeastern China. Kappa indexes above 0.85 for the validation period verify that the coupled land use change model is able to simulate the effect of the abatement actions on land use. Scenario predictions reveals that local emigration and a comprehensive ecological restoration project as abatement actions could significantly decrease contents of P in receiving surface waters: Relative to year 2012, total P and orthophosphate could be reduced by 36 and 45 %, respectively, by the end of year 2018. This modelling approach can, with moderate modifications, also be adapted to other watersheds. The model developed in this study can thus be used by environmental managers as a tool to identify risk for P loss from diffuse sources within a watershed and assist policy makers to assess the effect on P losses by implementing abatement actions that changes land use.

Metals are significant environmental pollutants, and their toxicity is a problem for all living organisms. Indeed, aquatic plants are particularly sensitive to the excess of metal ions. Several researches report that aquatic plants exposed to metal-induced toxicity showed similar responses (e.g. inhibition of growth and induction of oxidative stress). Meanwhile, many studies were involved to counter these toxicities. This paper provides a brief review of the role of the exogenous supply of some compounds in the alleviation or reduction of toxicity in aquatic plants generated by metals. Particular attention is given to the role of polyamine, proline, nitric oxide, glutathione and phytochelatin.

Studies on ion movement in soil profiles associated to the application of vinasse are scarce. The objective of this study is to assess the quantity of inorganic and organic ions in the profile of the soil under sugarcane. The study was realized in a commercial sugarcane cultivar in the municipality of Ponta Pora, MS, Brazil in the harvest year of 2010/2011. The soil in the experimental area was classified as Haplorthox clay. The experimental design was randomized blocks, with four repetitions, two depths, and four harvest periods, after application of a 350 m³ h⁻¹ vinasse dosage. Twenty-four soil solution extractors were installed at a distance of 4 × 4 m from each other in the areas under vinasse treatment. Vinasse was chemically characterized by the inductively coupled plasma atomic emission spectrometry method. The extracted solution samples were determined for ionic chromatography. Elevated concentrations of lactic, butyric, citric, tartaric, succinic, formic, and acetic acids were found up to 1 m of depth up to 29 days after application. After 63 days, no traces of those anions were found in the soil. There was a rise in nitrate and a decline in the content of chloride and sulfate.

This research work evaluates the use of hydrogen peroxide for the removal of cyanide from coking wastewater deriving from the washing of gases in coal combustion furnace. The effect of the presence or absence of suspended solids and organic micropollutants on the efficiency of the treatment is analyzed. Various dosages of hydrogen peroxide (6.5–200 mg/L) were added to both aqueous solution (at pH 10.5) and industrial wastewater (at pH 10.3) samples. The influence of suspended solids in coking wastewater was analyzed by applying a coagulation–flocculation–decantation process before the hydrogen peroxide treatment. The preliminary cyanide removal treatment in aqueous solution showed that the maximum cyanide removal did not exceed 14 % using a mass ratio of hydrogen peroxide to cyanide of 11.6. The maximum cyanide removal obtained in coking wastewater was 47 % with a mass ratio of hydrogen peroxide to cyanide of 12.2 provided that a coagulation–flocculation–decantation pretreatment was applied to remove the suspended solids composed mainly of coal, calcium carbonate, and magnesium carbonate. On the other hand, the cyanide removal treatment in coking wastewater with hydrogen peroxide showed promising results in the removing of different organic micropollutants formed mainly by polycyclic aromatic hydrocarbons and quinolines.