Two Co oxide catalysts supported on natural zeolites from Indonesia (INZ) and Australia (ANZ) were prepared and used to activate peroxymonosulphate for degradation of aqueous phenol. The two catalysts were characterized by several techniques such as X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy (EDS) and N2 adsorption. It was found that Co/INZ and Co/ANZ are effective in activation of peroxymonosulphate to produce sulphate radicals for phenol degradation. Co/INZ and Co/ANZ could remove phenol up to 100 and 70 %, respectively, at the conditions of 25 ppm phenol (500 mL), 0.2 g catalyst, 1 g oxone and 25 C. Several parameters such as amount of catalyst loading, phenol concentration, oxidant concentration and temperature were found to be the key factors influencing phenol degradation. A pseudo first order would fit to phenol degradation kinetics, and the activation energies on Co/INZ and Co/ANZ were obtained as 52.4 and 61.3 kJ/mol, respectively. © 2013 Springer Science+Business Media Dordrecht.

Imperata cylindrica leaf was used as raw material to prepare two different adsorbents through chemical modification by using sulfuric acid and phosphoric acid. These two adsorbents, sulfuric acid-modified I. cylindrica leaf-based adsorbent (SIC) and phosphoric acid-modified I. cylindrica leaf-based adsorbent (PIC), were used to adsorb nickel ions (Ni²⁺) from aqueous solutions. The I. cylindrica leaf-based adsorbent and modified I. cylindrica leaf-based adsorbents were characterized by Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM). Different operational parameters such as initial solution pH, adsorbent size, adsorbent dosage, initial Ni²⁺ ion concentration, and temperature were studied. The adsorption isotherm and the adsorption kinetics were studied systematically. Based on the FT-IR spectrum before and after adsorption of Ni²⁺ ions, the adsorption mechanism involved both ion exchange and complexation between Ni²⁺ ions and functional groups on the surface of adsorbents. There was no sulfur and phosphorus detected in the aqueous solutions after adsorption. Therefore, SIC and PIC are effective in adsorbing Ni²⁺ ions and will not cause secondary pollution to the environment.

There are concerns over the environmental risks posed by Cu-based fungicide use, and there is community and regulatory pressure on viticultural industries to restrict the use of Cu-based fungicides. This study assesses the relative environmental risks posed by Cu-based and alternative synthetic organic fungicide compounds used in Australian vineyards, giving particular consideration to their adverse effects on soil microbial activity and how risks vary across different viticultural regions. The study was guided by key steps in the ecological risk assessment framework to analyse the risks of Cu-based fungicides towards soil organisms and involved four key steps: (1) problem formulation, (2) analysis (characterise exposure and effects), (3) risk characterisation and (4) risk assessment. There is evidence of a build-up of Cu-based fungicide residues in Australian vineyard soils, although this has occurred over many years, thus allowing the availability of Cu in the soil to be attenuated over time due to aging processes. On the whole, it appears that Cu-based fungicide residues are currently unlikely to pose a significant risk to soil organisms in Australian vineyard soils. However, there are indicators that continued applications of Cu-based fungicides may well have implications on the use of impacted land for sustainable agricultural production. Further detailed studies are required to enable a more definitive characterisation of the risks posed by Cu-based fungicide residues, such as establishing a clearer link between the laboratory and agricultural settings, investigating effects on other indicators of microbial activity and biodiversity and understanding the resilience of soil microbes to additional stressors. The challenge for agricultural industries and governments, both in Australia and globally, is to formulate appropriate plans to reduce the risks associated with Cu-based fungicide use. Further research is required to consider the relative risks of a wide range of alternative fungicide compounds to ensure that they pose a lower environmental risk than the Cu-based fungicides they may replace.

We investigated the influence of immobilization of bacterial cells and photocatalytic material TiO2 on the degradation of phenol by conducting batch microcosm studies consisting of suspended, immobilized cells and immobilized TiO2 at various initial phenol concentrations (50-1,000 mg L-1). Results showed that both suspended and immobilized cells were concentration-dependent, exhibiting the increasing degradation rate with the concentration of up to 500 mg L-1 above which it declined. The degradation rate of 0.39-3.47 mg L-1 h-1 by suspended cells was comparable with those of the literature. Comparison of the degradation rates between suspended, immobilized cells and immobilized TiO2 revealed that immobilized cells achieved the highest degradation rate followed by immobilized TiO2 and suspended cells due to the toxicity of phenol at the high concentration of 1,000 mg L-1. This indicates that immobilization of bacterial cells or photocatalytic materials can serve a better alternative to offer the higher degradation efficiency at high phenol concentrations. © 2013 Springer Science+Business Media Dordrecht.

In this study, the performance of a laboratory-scale soil aquifer treatment (SAT) system was investigated and treatability studies were done in order to determine organic matter removal from synthetic wastewater (SWW) and secondary treated real wastewater (RWW). The SAT system was constructed in laboratory conditions and treatability studies were conducted using soil columns, which were packed with silt loam soil samples. Each column was equipped with a series of ports at multiple depths from soil surface (10, 20, 30, 50, and 75 cm) to collect water samples. Two operational cycles were applied to represent the influence of different wetting and drying periods during wastewater application. Dissolved oxygen, chemical oxygen demand (COD), and total organic carbon (TOC) concentrations were measured in all samples. Average removal values of 61.4 % (COD) and 68.2 % (TOC) were achieved by in SWW and of 58.3 % (COD) and 51.1 % (TOC) in RWW in 55 and 25 weeks of operation, respectively. These results indicated that the performance of the columns operated with SWW was better than the performance of the columns operated with RWW. In essence, the easily biodegradable portion of organic matter was quickly consumed by microorganisms in the first 10 cm of the columns where oxygen levels peaked. Complex organic compounds that are likely to be found in RWW could thus be removed when longer residence times were achieved through the columns. When the removal performances achieved with different operating cycles were compared for each wastewater, it could be seen that longer wetting and longer drying periods yielded higher removal efficiencies in RWW and vice versa in SWW. © 2013 Springer Science+Business Media Dordrecht.

Traces of short- and long-lived fallout ¹³⁴Cs and ¹³⁷Cs were found in surface soil (volcanic ash soil) under a cool-temperate deciduous stand at Tomakomai Experimental Forest in Hokkaido, Japan after the Fukushima nuclear accident in March 2011. Most of them were present in the uppermost 5–6 cm of the soil. Mean concentrations of ¹³⁴Cs and ¹³⁷Cs were found to be 2.4 (±0.3) and 89 (±2) Bq Kg⁻¹ in May, and 6.9 (±0.4) and 94 (±2) Bq Kg⁻¹ in November 2011, respectively. A small increase in radiocesium concentration may result from biological activity in the uppermost portion of the soil in which fallout nuclides derived from the Fukushima NPP would not have existed in May. They were supposed to be fallen down on the fresh litter layer in the previous year. The results of a sequential extraction experiment with 1 M CH₃COONH₄ solution showed that desorption of radiocesium from the soil was difficult and not simple ion exchange processes.

This paper addresses the geochemical evolution, volumetric water content, and temperature of porewater when constructing different soil layers to improve the surface acidic conditions on a slope at a closed mine. Three cases were set under different layer systems. Case 1 was solely composed of surface-weathered rocks. A vegetation layer was constructed on the surface rocks in case 2, whereas a top vegetation and bottom low-permeable layers were constructed on the rocks in case 3. In both cases, a soil–cement layer was constructed to prevent landslides. Porewater sampling systems and soil sensors were set at different depths to collect porewater and measure the volumetric water content and temperature. The results showed that, when no layers were applied (case 1), high concentrations of heavy metals and low pH values were observed regardless of the depth and season. When a vegetation layer (case 2) was applied, a dramatic decrease in heavy metal concentrations was observed, similar to the results in case 3. In both cases, pH values were circumneutral. Moreover, the addition of the low-permeable layer reduced the infiltration of rainfall through the layers by considering the changes in volumetric water content. Also, the results of case 1 were compared with those obtained at a flat surface under similar conditions. On the slope, the pH was more acidic, and heavy metal concentrations were higher. These suggest that the dissolution of heavy metals from the weathered rocks into the porewater is enhanced on the sloping surface due to a longer solid–liquid interaction time.

Boric acid-treated and sulfur ion-doped multi-modified TiO₂ films with high photocatalytic activities were prepared on soda–lime glass (Na₂O · CaO · 6SiO₂) substrates via the sol–gel method. The as-prepared specimens were characterized using high-resolution field emission scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, photoluminescence spectra, UV–vis diffuse reflectance spectroscopy, and Brunauer–Emmett–Teller surface area. The photocatalytic activities of the films were evaluated by degradation of organic dyes in aqueous solutions. Compared with boric acid treatment and sulfur surface doping, the integration of both methods gave the best results. It is believed that high photocatalytic activity is correlated with the microstructure of the TiO₂ film.

Adsorption potentials of native and amine-modified plant biomass of Alyssum caricum for the removal of Reactive Green 19 (RG-19) and Reactive Red 2 (RR-2) dyes from aqueous solutions were studied. The adsorbents were characterized before and after modification process using Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET) and potentiometric titration analysis. Modification of the surface of A. caricum biomass with hexamethylenediamine (HMDA) showed an increase of 1.18-fold in its surface area. Batch studies illustrated that dye adsorption were highly dependent on different process variables, pH, initial dye concentration of solution, adsorbent dosage, and temperature. The maximum adsorption capacities of the native and amine-modified adsorbents were 27.6 and 63.4 mg/g adsorbent for RG-19 dye and 16.5 and 36.8 mg/g adsorbent for RR-2 dye, respectively. The adsorption of both dyes on the native and amine-modified plant biomass correlated well with the Langmuir and Temkin isotherm equations as compared to Freundlich and D-R equations. The calculated thermodynamic parameters for both native and amine-modified adsorbents showed that the adsorption was feasible, spontaneous, and exothermic. The information gained from these studies was expected to indicate whether native and amine-modified adsorbents can have potential to be used for the removal of other dyes from wastewaters. © 2013 Springer Science+Business Media Dordrecht.

This research evaluated the effects of alkyl polyglucoside (APG), an environment-friendly surfactant, on the removal of anthracene (ANT), phenanthrene (PHE), and pyrene (PYR) from the soil cultivated with Scirpus triqueter, an aquatic native pioneer plant in the Yangtze estuarine wetland, China. Soils spiked with about 200 mg kg-1 of ANT, PHE, and PYR were individually irrigated with 0, 10, 20, 30, 40, 50, 100, and 150 mg L -1 of APG. Plant biomass yields, polycyclic aromatic hydrocarbons (PAHs) removal rates, soil microbial, and soil enzyme activities were quantified after 90 days' cultivation of Scirpus triqueter. Experiments demonstrated that APG has an ability to facilitate PAHs degradation at appropriate concentrations. The highest removal rate of the PAHs was observed in 40 mg L-1 APG treatment, and the removal rates increased 23, 54, and 52 %, respectively, compared to the non-amended control pots. However, the PAHs removal rate decreased to a certain extent when high concentrations of APG were added. The effect on PAHs removal in the soil could be explained by the changed levels of plant biomass, soil microbial populations, and soil enzymatic activity affected by the APG. The results suggested that the use of Scirpus triqueter combined with APG was an effective means for the phytoremediation of the PAH-contaminated soil. At the same time, APG's optimal concentration should be determined before the application in the PAH-contaminated wetlands. © 2013 Springer Science+Business Media Dordrecht.