This work discusses the preparation and characterizations of glass hollow fiber membranes prepared using zeolite-5A as a starting material. Zeolite was formed into a hollow fiber configuration using the phase inversion technique. It was later sintered at high temperatures to burn off organic materials and change the zeolite into glass membrane. A preliminary study, that used thermogravimetric analysis (TGA), X-ray diffraction (XRD), and Fourier transform infrared (FTIR), confirmed that zeolite used in this study changed to glass at temperatures above 1000 °C. The glass hollow fiber membranes prepared using the phase inversion technique has three different microstructures, namely (i) sandwich-like structure that originates from inner layer, (ii) sandwich-like that originates from outer layer, and (iii) symmetric sponge like. These variations were influenced by zeolite weight loading and the flow rate of water used to form the lumen. The separation performances of the glass hollow fiber membrane were studied using the pure water permeability and the rejection test of bovine serum albumin (BSA). The glass hollow fiber membrane prepared from using 48 wt% zeolite loading and bore fluid with 9 mL min⁻¹ flow rate has the highest BSA rejection of 85% with the water permeability of 0.7 L m⁻² h⁻¹ bar⁻¹. The results showed that the separation performance of glass hollow fiber membranes was in the ultrafiltration range, enabled the retention of solutes with molecular sizes larger than 67 kDa such as milk proteins, endotoxin pyrogen, virus, and colloidal silica.

Salt stress is one of the most dramatic abiotic stresses that induce oxidative and osmotic stress simultaneously. Salt stress is known to be more effective in reducing growth and yield of glycophytes; however, halophytes are able to withstand salt stress. Nonetheless, variability exists among different halophytic plants species from different plant families. Chenopodium album belongs to Chenopodiacea family and is known as weed in many regions of world; however, it is a very interesting halophytic plant. Little research has conducted so far by considering C. album as model plant to study salt stress tolerance mechanisms. This article attempts to compile current literature in order to explain C. album salt stress tolerance mechanism and to highlight the knowledge gap relating to salt stress tolerance mechanism in C. album. Briefly, C. album has remarkable ability of seed dimorphism, sodium exclusion, and potassium retention. C. album further tolerates salt stress by increasing redox potential associated with high production of osmolytes and antioxidants.

This research focuses on the removal of heavy metal ions from aqueous solutions using magnetic chitosan hydrogel beads as a potential sorbent. Highly porous magnetic chitosan hydrogel (PMCH) beads were prepared by a combination of in situ co-precipitation and sodium citrate cross-linking. Fourier transform infrared spectroscopy indicated that the high sorption efficiency of metal cations is attributable to the hydroxyl, amino, and carboxyl groups in PMCH beads. Thermogravimetric analysis demonstrated that introducing Fe₃O₄ nanoparticles increases the thermal stability of the adsorbent. Laser confocal microscopy revealed highly uniform porous structure of the resultant PMCH beads, which contained a high moisture content (93%). Transmission electron microscopy micrographs showed that the Fe₃O₄ nanoparticles, with a mean diameter of 5 ± 2 nm, were well dispersed inside the chitosan beads. Batch adsorption experiments and adsorption kinetic analysis revealed that the adsorption process obeys a pseudo-second-order model. Isotherm data were satisfactorily described by the Langmuir equation, and the maximum adsorption capacity of the adsorbent was 84.02 mg/g. Energy-dispersive X-ray spectroscopy and X-ray photoelectron spectra analyses were performed to confirm the adsorption of Pb²⁺ and to identify the adsorption mechanism.

In this study, the metabolic effects of waterborne exposure of medaka (Oryzias latipes) to nominal concentrations of 20 (L group) and 2000 μg/L (H group) 2,4-dichlorophenol (DCP) were examined using a gas chromatography/mass spectroscopy (GC/MS) metabolomics approach. A principal component analysis (PCA) separated the L, H, and control groups along PC1 to explain the toxic effects of DCP at 24 h of exposure. Furthermore, the L and H groups were separated along PC1 at 96 h on the PCA score plots. These results suggest that the effects of DCP depended on exposure concentration and time. Changes in tricarboxylic cycle metabolites suggested that fish exposed to 2,4-DCP require more energy to metabolize and eliminate DCP, particularly at 96 h of exposure. A time-dependent response in the fish exposed to DCP was observed in the GC/MS data, suggesting that the higher DCP concentration had greater effects at 24 h than those observed in response to the lower concentration. In addition, several essential amino acids (arginine, histidine, lysine, isoleucine, leucine, methionine, phenylalanine, threonine, tryptophan, and valine) decreased after DCP exposure in the H group, and starvation condition and high concentration exposure of DCP could consume excess energy from amino acids.

The health, environmental and socio-economic issues related to the massive use of plant protection products are a concern for all the stakeholders involved in the agricultural sector. These stakeholders, including farmers and territorial actors, have expressed a need for decision-support tools for the management of diffuse pollution related to plant protection practices and their impacts. To meet the needs expressed by the public authorities and the territorial actors for such decision-support tools, we have developed a technical-economic model “OptiPhy” for risk mitigation based on indicators of pesticide toxicity risk to applicator health (IRSA) and to the environment (IRTE), under the constraint of suitable economic outcomes. This technical-economic optimisation model is based on linear programming techniques and offers various scenarios to help the different actors in choosing plant protection products, depending on their different levels of constraints and aspirations. The health and environmental risk indicators can be broken down into sub-indicators so that management can be tailored to the context. This model for technical-economic optimisation and management of plant protection practices can analyse scenarios for the reduction of pesticide-related risks by proposing combinations of substitution PPPs, according to criteria of efficiency, economic performance and vulnerability of the natural environment. The results of the scenarios obtained on real ITKs in different cropping systems show that it is possible to reduce the PPP pressure (TFI) and reduce toxicity risks to applicator health (IRSA) and to the environment (IRTE) by up to approximately 50 %.

Inorganic fertilizers are used as agricultural countermeasures intended to inhibit the soil to plant transfer of radionuclides after a radioactive fallout. Two NH₄ ⁺ fertilizers, diammonium phosphate (DAP) and NPK, were applied to soil contaminated with a mixture of radionuclides to analyze whether they modify the transfer of ¹³⁷Cs, ⁹⁰Sr, and ⁶⁰Co and stable elements (K, Na, Ca, and Mg) to wheat plantlets grown under controlled laboratory conditions. DAP introduced NH₄ ⁺ in the soil, which can increase ¹³⁷Cs transfer, while NPK also introduced K⁺, which can decrease it. The application of DAP increased the accumulation of ¹³⁷Cs in wheat plantlets with increasing application rate, so did the ¹³⁷Cs/K in plantlets. Regarding the NPK application, the ¹³⁷Cs increased in all treatments, but at maximum rate, the available K introduced by the fertilizer was probably able to partially satisfy the nutritional requirements of the wheat plantlet and the ¹³⁷Cs decreased relative to the recommended rate. The ¹³⁷Cs/K ratio in plantlet decreased with increasing NPK rates. The transfer of ⁹⁰Sr increased with increasing DAP rate and only at the maximum NPK rate. The ⁶⁰Co transfer only increased at the maximum application rates for DAP and NPK. These modifications should be considered when using these fertilizers as agricultural countermeasures.

Manganese-rich MnSAPO-34 molecular sieves were prepared by one-pot synthesis method for NO ₓ abatement using the ammonia-selective catalytic reduction (NH₃-SCR) technology and characterized using ICP, BET, XRD, FE-SEM, H₂-TPR, NH₃-TPD, XPS, and DR UV-Vis analyses. The experimental results indicate that the Mn content and chemical state, as well as the surface acidity, of the MnSAPO-34 molecular sieves significantly enhance their DeNO ₓ efficiency at low temperatures (ca. 200–300 °C). The manganese-rich MnSAPO-34 was synthesized using a combination of triethylamine and diisopropylamine as the structural directing agents and high Mn loading (n(MnO)/n(P₂O₅) = 0.4). The resulting catalyst exhibits the highest activity among all of the samples with a NO ₓ conversion value of nearly 95% and a N₂ selectivity that is higher than 90% at 220–400 °C. In addition, this catalyst presents higher NO ₓ conversion than the conventional V₂O₅-WO₃/TiO₂ catalysts and other SAPO-based catalysts below 300 °C. Furthermore, the analytical results indicate that the manganese species in the catalyst are mainly in the form of a framework Mn(IV), which could play a significant role in the NH₃-SCR process as the specific active species. The results suggest that controlling the types and content of the organic amine templates and variations in the surface acidity of the catalysts may significantly enhance the SCR activity at lower temperatures.

To determine the potential effects of seasonal changes on water temperature and water quality upon removal of ammonium and organic carbon pollutants and to characterize the variations in microbial characteristics, a pilot-scale activated carbon filter biologically enhanced with heterotrophic nitrifying bacteria was investigated for 528 days. The results show that 69.2 ± 28.6% of ammonium and 23.1 ± 11.6% of the dissolved organic carbon were removed by the biologically enhanced activated carbon (BEAC) reactor. It is shown that higher biodegradable dissolved organic carbon enhances ammonium removal, even at low temperatures. The C/N ratio consumed by the BEAC reactor reached a steady value (i.e., 3.3) after 2 months of operation. Despite seasonal fluctuations and competition of the indigenous community, the heterotrophic nitrifying bacteria (Acinetobacter sp. HRBLi 16 and Acinetobacter harbinensis strain HITLi 7) remained relatively stable. The amount of carbon source was the most significant environmental parameter and dramatically affected the microbial community compositions in the BEAC reactor. The present study provides new insights into the application of a BEAC reactor for ammonium removal from drinking water, resisting strong seasonal changes.

The accelerated growth trajectory of waste electrical and electronic equipment (WEEE) is a matter of concern for governments worldwide. In developing countries, the problem is more complex because municipal waste management is still a challenge for municipalities. Fernando de Noronha Island, an environmentally protected area, has a transfer station for solid waste before it is sent to the final destination abroad, which is different waste management model to most urban areas. In order to check the specifics of management of WEEE, this study aimed to qualitatively and quantitatively evaluate the generation of this type of waste on the main island of Fernando de Noronha, taking into consideration aspects related to consumption habits and handling of waste. During the in situ research, a questionnaire was applied to a sample of 83 households. The results provide a picture of the generation of WEEE for a period of 1 year, when a production of 1.3 tons of WEEE was estimated. Relationships between education level and monthly income and between education level and number of plasma/LCD TVs and washing machines were confirmed. Another important result is that only two socioeconomic variables (monthly income and education level) are related to two recycling behavior variables. In addition, the population and government treat WEEE as ordinary waste, ignoring its contaminant potential. Despite the existence of relevant legislation concerning the treatment and disposal of WEEE, additional efforts will be required by the government in order to properly manage this type of waste on the island.

Rapid urbanization and industrialization may cause increased exposure levels to potential toxic trace elements (PTEs) and associated health risks for population living in cities. The main objectives of this study are to investigate systematically the occurrence, source, fate, and risk of PTE contamination from industrial influence in Baoji urban soil. Seven PTE levels (Pb, Zn, Cu, Cr, V, Sb, and As) were surveyed in 50 composite samples from Baoji urban soil by wavelength dispersive X-ray fluorescence spectrometry. Results reveal that the long-term industrial activities have increased PTEs Pb (409.20 mg/kg mean value), Cu (107.19 mg/kg mean value), Zn (374.47 mg/kg mean value), and Sb (26.00 mg/kg mean value) to enrich in urban soil at the different extents. The same results concur with the significant similarity of spatial distribution patterns of Pb, Zn, Cu, and Sb (slightly similar distribution) interpolated by GIS, implying a considerable Pb, Zn, Cu, and Sb contamination pool in urban soil disturbance from local metallic industrial activities. Whereas As in study area mainly controls parent material leaching and therefore has natural sources. Cr and V with the heterogeneous spatial distributions are possibly inclined to coal combustion sources. Those conclusions are also confirmed by the results of multivariate analysis. The chemical forms of PTEs fractionated by BCR three-stage sequential extraction procedure show that Pb and Cu are highly associated to the reducible phase (62.55 and 36.41%, respectively). However, Zn is highly associated to the oxidizable phase (33.68%), and a significant concentration is associated to acid and water extractable fractionation of 15.93% for Zn and 34.40% for Pb. In contrast, As, Cr, V, and Sb are mainly bound to the residual phase (>65% for all elements) with low concentrations retained to water extractable fractionation. The health risk assessed by a new classification Modified Integrate Risk Assessment Code (MI-RAC) reveals that the Pb poses the extremely high risk for human health than others. The results of PTE leaching in organic acids (artificial chelating agent and LMMOAs) indicate that low pH and more carboxyl groups of organic acid can quickly increase the PTEs release from soil and induce more mobility. By comparison, DTPA and EDTA are the effective extractant for Pb and Sb. The leaching kinetics of most PTEs are best described with the Elovich equation model and which involve the ligand exchange (LE) and ligand-enhanced dissolution (LED) two major process. It is a conclusion that long-term metallic industrial activities would accelerate the PTE accumulations in Baoji urban soil and enhance their mobility in a local scale. The considerable mobility and extremely high risk of Pb in Baoji ecoenvironment should be paid more attentions, and the phytoremediation with organic acid leaching assistant could be used to reduce total metal content of multiPTE contaminants in Baoji soils. The research will give the scientific knowledge for controlling the pollution of PTEs in urban soil and can be used as guidance to control the soil pollution in similar cities worldwide.