Eco-friendly nanoparticles: mechanisms and capacities for efficient removal of heavy metals and phosphate from water using definitive screening design approach.

Can nano-zero-valent iron, synthesized using oak leaf extract, be the key solution for water preservation, efficiently removing heavy metal ions and phosphate anions simultaneously? This research unveils how this technology not only promises high efficiency in the remediation of water resources, but also sets new standards for environmentally friendly processes. The high antioxidant capacity and high phenol content indicate suggest the possibility of oak-nZVI synthesis using oak leaf extract as a stable material with minimal agglomeration. The simultaneous removal of Cd and phosphates, as well as and Ni and phosphates was optimized by a statistically designed experiment with a definitive screening design approach. By defining the key factors with the most significant impact, a more efficient and faster method is achieved, improving the economic sustainability of the research by minimizing the number of experiments while maximizing precision. In terms of significance, four input parameters affecting process productivity were monitored: initial metal concentration (1-9 mg L-1), initial ion concentration (1-9 mg L-1), pH value (2-10), and oak-nZVI dosage (2-16 mL). The process optimization resulted in the highest simultaneous removal efficiency of 98.99 and 87.30% for cadmium and phosphate ions, respectively. The highest efficiency for the simultaneous removal of nickel and phosphate ions was 93.44 and 96.75%, respectively. The optimization process fits within the confidence intervals, which confirms the assumption that the selected regression model well describes the process. In the context of e of the challenges and problems of environmental protection, this work has shown considerable potential and successful application for the simultaneous removal of Cd(II) and Ni(II) in the presence of phosphates from water.

Electrocoagulation in treatment of municipal wastewater- life cycle impact assessment.

The purpose of this study is investigation of electrocoagulation (EC) as a treatment of municipal wastewater, integrating life cycle impact assessment (LCIA) for assessing its environmental performance of investigated treatment. The study evaluated the effectiveness of EC in removing physico-chemical and microbial parameters using aluminum (Al) and iron (Fe) electrodes in monopolar and bipolar modes. Bipolar arrangement of Al(-)/Al/Al/Al(+) electrodes achieved the highest removals: 70% COD, 72% BOD5 followed by complete elimination of total phosphorous, turbidity and microbial parameters. This treatment was subject to investigation of the influence of reaction time (t = 10-60 min) on removals at higher current density (CD = 3.33 mA/cm2). In order to reduce energy consumption, the same reaction time range was used with a reduced CD = 2.33 mA/cm2. Following removal efficiencies obtained: 47-72% COD (higher CD) and 53-78% (lower CD); 69-75% BOD5 (higher CD) and 55-74% CD (lower CD); 12-21% NH4- (higher CD) and 7-22% NH4- (lower CD). Total P, NO3- and NO2- compounds showed the same removals regardless the CD. Decrease in current density did not influence removals of total suspended matter, turbidity, salinity as well as microbial parameters. The bipolar arrangement of Al(-)/Al/Al/Al(+) electrodes, assuming a lower CD = 2.33 mA/cm2 and t = 30 min, was assessed with the Recipe 2016Midpoint (H) and USEtox v.2 LCIA methods to explore the environmental justification of using EC for wastewater treatment. The LCIA results revealed that the EC process significantly reduces water eutrophication and toxicity for freshwater and marine ecosystems, but has higher impacts in global warming, fossil fuel consumption, human toxicity, acidification, and terrestrial ecotoxicity due to high energy consumption. This can be mainly explained by the assumption in the study that the EC precipitate is dispersed to agricultural soil without any pre-treatment and material recovery, along with relatively high energy consumption during the process.

Integrated application of green zero-valent iron and electrokinetic remediation of metal-polluted sediment.

In recent years, more focus has been placed on integrated metal removal processes. Electrokinetic (EK) treatment is superior to other technologies because it can be applied to a variety of mediums. Green nanoparticles, on the other hand, have the potential to significantly reduce pollutant concentrations in a short period of time. In this study, we investigated the possibility of combining green zero-valent iron (nZVI) with EK on Cd and Zn-contaminated sediment. For green synthesis, extracts of dry leaves of mulberry (ML-nZVI) and oak (OL-nZVI) were used, both abundantly present in the Republic of Serbia. The results show that, despite the fact that their availability was greatly reduced, the metals were concentrated and stabilized to a significant extent in the middle of the EK cell (z/L 0.5) after all treatments. When the results were compared, OL-nZVI proved to be a more effective nanomaterial even with smaller doses of OL-nZVI, which is important in terms of achieving better economic benefits. This study identified green nano zero-valent iron as a powerful tool for metal removal when combined with electrokinetic (EK) treatment, which improves green nZVI longevity and migration. This study of the combined green nZVI-EK remediation treatment, in particular, will have an impact on future research in this field, given the achieved efficiency.

A cost effective method for immobilization of Cu and Ni polluted river sediment with nZVI synthesized from leaf extract.

This study investigates the performance of oak (OL) and mulberry (ML) leaves for synthesized of nanoscale zero-valent iron (nZVI), in immobilizing Cu and Ni in contaminated sediment. Characterization of synthesized Fe nanoparticles from oak and mulberry leaf extracts demonstrated that they are nontoxic and stabile nanomaterials for application in the sediment remediation. Effectiveness of stabilization process was performed by microwave-assisted sequential extraction procedure (MWSE) and single-step leaching tests which have been applied to evaluate the metal extraction potential. This research showed that OL-nZVI and ML-nZVI were effective in transforming available Cu and Ni to stable fraction. The maximum residual percentage of Cu increased by 76% and 73%, and for Ni 81% and 80%, respectively, with addition of 5% OL-nZVI and 5% ML-nZVI. Used single-step leaching tests (Toxicity Characteristic Leaching Procedure-TCLP and German standard test- DIN) indicated that all stabilized samples can be considered as non-hazardous waste, as all leached metal concentrations met the appropriate set criteria. Cost analysis showed that the operating cost for contaminated sediment treatment with green synthesized nZVI are 50.37 €/m3/per year. This work provides a new insight into the immobilization mechanism and environmental impact of Cu and Ni in contaminated sediment and potential way of treatment with OL-nZVI and ML-nZVI. Generally, nZVI can be an effective and versatile tool for stabilization of sediment polluted with toxic metals.

Long-term application of stabilization/solidification technique on highly contaminated sediments with environment risk assessment.

After dredging of contaminated sediment, additional remediation technique is required before its final disposal. For this purpose, this research was based on the long-term stabilization/solidification (S/S) process of highly contaminated sediment (dominantly by heavy metals) from a European environmental hot spot, the Great Backa Canal. Due to optimisation of remediation techniques, this sediment is treated with selected immobilization agents: kaolinite, quicklime and Portland cement. The use of pseudo-total metal content (selected priority substances: Cr, Ni, Cu, Cd, Zn, Pb and As) in untreated sediment, determined that sediment urgently requires remediation. Short-term (after 7 and 28 days) and long-term (after 7 years) monitoring were done in order to estimate the concentrations of metals and effect on biota from S/S mixtures during this processes. The environmental risk assessment encompassed the application of several appropriate analytical methods: the pseudo-total metal content, the German standard leaching test - DIN 3841-4 S4 and Toxicity Characteristic Leaching Procedure - TCLP test leaching tests and sequential extraction procedure (BCR) on S/S mixtures, testing the aging process and toxicity effects. After simulating real environmental conditions using all tests in all three mixtures, metals do not exceed the prescribed limit values and as such S/S mixtures are classified as non-hazardous waste. Sequential extraction procedure showed that the highest percentage of metals are in the residual phase, bound to silicates and crystalline structure. After 7 years of S/S mixture aging, kaolinite showed the highest binding capacity that was reflected in the content of metals in the residual phase (34.8% of Ni to 77.6% of Cr). DIN and TCLP leaching tests confirmed that the exchangeable phase has a minor effect on the environment. Accordingly, this remediation technology could be well applied for final disposal of this and similar extremely contaminated sediment dominantly with inorganic pollutants.

Removal of diclofenac from water by in/out PAC/UF hybrid process.

Results from a lab-scale investigation of a hybrid in/out ultrafiltration and powdered activated carbon adsorption PAC/UF for removal of diclofenac (c0 = 5 mg/L) are presented. The efficiency of the process was compared for single pulse and continuous carbon dosing (PAC dose 5 mg/L) in dechlorinated tap water under fluxes of 87 and 135 L/(m2 h). For higher flux conditions, it was observed that single pulse dosing has an advantage over continuous dosing procedure when comparing cycle average removal efficiency. Increase of carbon dose under these conditions increased cycle average removal only to a limited extent. PAC dose above 15 mg/L did not give improvements of the removal. Hypothesis was made that non-effective carbon distribution might be the possible reason.

Some arguments in favor of a Myriophyllum aquaticum growth inhibition test in a water-sediment system as an additional test in risk assessment of herbicides.

The present study compares the practicability, reproducibility, power, and sensitivity of a Myriophyllum aquaticum growth inhibition test in a water-sediment system with the recently accepted Myriophyllum spicatum test in an equivalent testing system and the standard Lemna sp. test. Special consideration was given to endpoints based on M. aquaticum control plant growth and variability of relative growth rate and yield: shoot length, fresh weight, dry weight, and root weight. Sensitivity analysis was based on tests performed with 3,5-dichlorophenol, atrazine, isoproturon, trifluralin, 2,4-dichlorophenoloxyacetic acid, and dicamba. Growth rates for average M. aquaticum control plants were 0.119 d(-1) and 0.112 d(-1), with average estimated doubling time 6.33 d and 6.74 d for relative growth rate fresh weight and shoot length, respectively. Intrinsic variability of M. aquaticum endpoints was low: 12.9%, 12.5%, and 17.8% for relative growth rate shoot length, relative growth rate fresh weight and yield fresh weight, respectively. The power of the test was fairly high. When the most sensitive endpoints were used for comparison, the 2 Myriophyllum species were similarly sensitive, more sensitive (in the case of auxin simulators), or at least equally sensitive as Lemna minor to other tested herbicides. The M. aquaticum 10-d test with a 7-d exposure period in a water-sediment system has acceptable sensitivity and can provide repeatable, reliable, and reproducible results; therefore, it should not be disregarded as a good and representative additional test in environmental risk assessment.