A new cotton-based hydrogel nanocomposite was successfully prepared by free radical graft copolymerization of acrylamide (AAm) and acrylonitrile (AN) onto fabric followed by insertion of Ag nanoparticles. Ammonium persulfate (APS) was used as an initiator in the presence of a cross-linker, methylene bisacrylamide (MBA). Fourier transform infrared, thermogravimetric analysis, scanning electron microscopy, X-ray diffraction, and transmission electron microscopy were employed to confirm the structure of the hydrogel nanocomposite. Initially, the affecting variables onto graft polymerization (i.e. AAm, AN, MBA, APS, and silver concentrations) were systematically optimized to achieve a hydrogel with swelling capacity as high as possible. The resulted nanocomposite exhibits superhydrophilic and superhydrophobic properties. Therefore, the grafted fabric selectively separated water from oil/water mixtures with high separation efficiency. The influences of filter type, percentage of coated hydrogel on cotton, presence of silver nanoparticles, pH of solution, extracted oil type, as well as hydrogel nanocomposite on the separation efficiency of filters were also studied in detail. Moreover, pH of zero point charge (pHzₚc) of the hydrogel nanocomposite was determined by alkaline titration method, and a value of 6.5 was obtained.

Preliminary analysis on dredged marine sediments from Benoi basin in Singapore was carried out showing elevated concentrations of Zn, Cu, Pb, Cd, Cr and Ni. Ethylenediamine tetraacetic acid (EDTA) thermal washing experiments were conducted for heavy metal extraction at temperature 100 °C. Results indicated the significant efficiency of thermal washing to extract Pb, Zn and Ni. However, there was little or no influence in the removal of Cu and Cr and a slight effect to Cd indicating multiple mechanisms. In addition, agitation was found to have great influence on the removal efficiency of heavy metals as experiments without agitation performed lesser or no extraction due to limited contact of the washing solution and the dredged sediment. Sequencing processes of thermal treatment followed by EDTA washing showed limited performance, likely due to thermal stabilization of the contaminants particularly at low liquid-to-soil (L/S) ratio. Furthermore, sequential extraction analysis on the metal speciation was performed before and after thermal washing. It was revealed that metals mainly extracted from fractions bound to carbonates and Fe-Mn oxides, the relative mobile fraction. On the contrary, metals in the residual fraction displayed a considerable stability.

The aim of this study was to investigate the effect of pH 4 and 7 on the cellular toxicity impact of silver nanoparticles (AgNPs) on the green alga Chlamydomonas acidophila. Changes in chlorophyll content, cellular viability, and reactive oxygen species (ROS) formation were determined permitting the characterization of the toxicity of AgNPs. Chemical characterization of AgNPs in suspension showed that nanoparticle size distribution was dependent to the pH of the culture medium, and a higher solubility was observed at pH 4 compared to that at pH 7. After 24 h of exposure, results indicated that the chlorophyll content and cellular viability decreased significantly, while the intracellular ROS production increased significantly, in relation to the increasing concentration of AgNPs (0.1–100 mg/L). Therefore, our results demonstrated that AgNP-induced toxicity was pH dependent as indicated by the cytotoxicity mediated through the induction of oxidative stress. In conclusion, the characterization of the physicochemical properties of AgNPs in aqueous solution having different pH is essential for the understanding of their toxicity impact on algal cells.

In this study, we investigated the microbiological quality of the small urban Zenne River which flows through the city of Brussels (Belgium). The abundances of faecal indicator bacteria (FIB) (Escherichia coli and intestinal enterococci) revealed high levels of faecal contamination of the Zenne River, especially in Brussels area and downstream from this area where FIB were in the range of what is usually observed in secondary treated wastewaters. The origin of this faecal contamination is mainly attributed to the effluents of the two wastewater treatment plants (WWTPs) located along the river in Brussels. Comparison of the present situation with the 1990s situation (before the implementation of Brussels WWTPs) showed a sharp improvement of the river microbiological quality. This improvement should however be regarded with care as it was also observed that, during rain events, combined sewer overflows (CSO) outfalls were responsible of a strong increase of faecal contamination in the river downstream from Brussels, and such CSO occur frequently in Brussels. Altogether, these results document the variations of the microbiological quality of a sewage-polluted urban river in relation with long-term changes (implementation of WWTP) and the short-term disturbances (CSO).

In the Mezquital valley, untreated wastewater (45 m³ s⁻¹) from Mexico City is used for the irrigation of around 900 km²of agricultural soil. High concentrations of metals including methylmercury (3.8 ± 2.5 ng l⁻¹) and lead (0.16 ± 0.05 mg l⁻¹) were measured in anoxic wastewater canals. Downstream, dissolved, and particulate polymetallic (Hg, Pb, Cr…) concentrations decreased by factors 10 to 1,000 in the Tula River (which received a mix of fresh and wastewater) due to the dilution and oxidation of surface water, and to the decrease of contaminants concentration in wastewater downstream irrigated soils. However, dissolved and particulate methylmercury concentrations (0.06 to 0.33 ng l⁻¹and 1.6 to 4.5 μg kg⁻¹, respectively) remained elevated in comparison to other natural hydrosystems. The monitoring of an irrigation event and the distribution of metals in a soil profile irrigated for more than 80 years showed that metals were retained in the draining tilled layer. The oxic conditions and slightly acidic pH (~6.5) in this layer were found favorable for metal adsorption and co-precipitation with redox-sensitive elements (Fe, Mn) and suggestively for mercury demethylation. In the downstream Tula River and groundwater, almost all metallic concentrations remained below guideline thresholds. Only, dissolved As and Pb concentrations remained two to five times above thresholds for drinking water, highlighting a potential health risk for approximately 500,000 people who use groundwater as water supply.

This paper presents a study of the combined process of adsorption and biodegradation in solid biologically activated carbon (AC) for the removal of salicylic acid aimed at determining the influence of the presence of biofilm on the process. Adsorption on AC and biodegradation of free cell cultures were studied separately so as to compare their performance with that of the combined biosorption system. The formation of bacterial biofilm on the surface of the carbon was investigated. The study was carried out using a range of synthetic solutions containing between 15 and 500 mg/L salicylic acid simulating an industrial effluent from the pharmaceutical industry. An individual bacterium, Pseudomonas putida (DSM 4478), was used to study the differentiated effects. Filtrasorb 400 and GAC 830 ACs were used in the adsorption processes and Filtrasorb 400 in the biofilm formation and combined biosorption processes. As regards, combined adsorption/biodegradation results indicated that the bioactivated carbon system outperformed the combination of conventional AC and biological water treatment processes when working with high pollutant concentrations.

The thiol-ene-based P(Penta3MP4/PEGDA/AAc) hydrogels were prepared by UV curing technique, then characterized and used as adsorbents for the investigation of the effect of process parameters such as pH of solution, contact time, and initial concentration of solution, on the removal of Ag(I) from aqueous solution. The results indicate that the adsorption of Ag(I) ions from aqueous solutions is strongly dependent on pH under experimental conditions. Both Langmuir and Freundlich isotherm models were applied to experimental data, and the results show that the adsorption process is well fitted to the Langmuir isotherm model. Selectivity, reusability, and applicability of hydrogels to radiographic film waste were investigated.

Anthropogenic activities such as industry, agriculture, and daily life are related to metal pollution of the environment. Places known of the highest impact are fishponds where intensive fish farming is believed to input a significant amount of various elements to water. Additionally, many studies suspect wetland hunting activity of water lead pollution. The present paper aims to check if hunting is a significant source of lead (Pb) in water as well as to study the temporal trends of numerous parameters (pH, SEC, Cd, Cu, Zn, Ca, Mg, Na, K, NH4+, HCO₃⁻, SO₄²⁻, Cl⁻, NO₃⁻, F⁻) in ponds (n = 48) and inflow (n = 24) waters near Zator in southern Poland, Europe. Most concentrations were measured with ion chromatography and electrothermal atomic absorption spectrometry. Lead concentrations in pond waters were low and found not to be linked with hunting activity, as well as they did not differ from the ones found in the inflow water. Moreover, it could be stated that activities led on ponds did not enrich rivers in the studied ions and elements.

The disposal of cyanogenic residues from the processing of cassava, during the flour production in certain regions of the Brazilian northeastern, has been a cause of concern in recent years, since this practice may lead to environmental imbalances. The results obtained in this work show a possible impact caused by the release of this kind of waste into water bodies, as well as its potential use as biofertilizer, mainly due to its high nutrient content. Humic substances (HS) from water and soil showed high interaction with cyanide ions (CN⁻), being the main responsible for the bioavailability of these ions into the environment. Furthermore, studies in microcosms propose viable and low-cost alternatives to decrease the levels of CN⁻ions in the liquid waste (called “manipueira”), as well as its potential use as biofertilizer.

In this study, the potential effects of three modified industrial by-products—modified low-grade phosphate rock with soda dregs (MP), modified flue gasses desulfurization residue (MF), and a mixture of MF and phosphoric acid (MFP)—were evaluated in the remediation of heavy metal-contaminated agricultural soil at four different treatment levels. The effects of the amendments on the extractability and phytoavailability of soil heavy metals were tested using a standardized sequential extraction test and a pakchoi pot experiment. The impacts of the three amendments on soil quality was investigated, including changes of soil pH, availability of K, Ca, Mg, Si and P, and the effects on pakchoi growth. The addition of these amendments resulted in a significant decrease of labile fraction of the heavy metals in soil (p < 0.05) and a marked decrease in heavy metal uptake by pakchoi (p < 0.05) in the pot experiment. All the amendments improved soil quality as measured by neutralization of soil acidity, increased content of mineral nutrients of soil (specifically, available K, Ca, Mg, Si, and/or P), and enhanced pakchoi growth when compared to the controls. Significant correlations (positive/negative) were observed among these factors, indicating multiple effects of the amendments on the remediation process. The increased soil pH and elevated mineral nutrients contributed to the stabilization of heavy metals, and the remediated soil conditions resulted in improved growth of pakchoi. These results suggest that all three of the modified industrial by-products could be used for the remediation and restoration of heavy metal-contaminated agricultural soil.