Inorganic nanoparticles enhance the production of reactive oxygen species (ROS) during the autoxidation of L-3,4-dihydroxyphenylalanine (L-dopa)

Public concerns over the toxicity of nanoparticles (NPs) are growing due to the rapid development of nanotechnology. An important mechanism of nanotoxicity is oxidative stress resulting from reactive oxygen species (ROS). In this study, the chemical production of ROS by inorganic NPs oxidizing the mammalian phenolic compound, l-3,4-dihydroxyphenylalanine (l-dopa) was evaluated using a ROS sensitive dye, 2′,7′-diclorodihydrofluorescin (DCFH). CeO₂, Fe₂O₃ and Fe⁰ NPs enhanced ROS production during the autoxidation of l-dopa by more than four-fold in reactions that were dependent on O₂. This is the first report of chemical ROS production due to interaction of phenolic compounds with NPs. Mn₂O₃ oxidized DCFH in a reaction that did not require O₂ or l-dopa, suggesting a direct redox reaction between the Mn₂O₃ and the dye. CeO₂, Mn₂O₃ and to a lesser extent Fe⁰ formed clear electron paramagnetic resonance (EPR) signature for hydroxyl radicals when incubated in aerobic aqueous suspensions with spin traps. The results indicate that NPs can generate ROS via chemical reactions with medium components and biomolecules susceptible to oxidation, such as l-dopa. NPs were reactive whereas micron-sized particles were not. The combined assay with l-dopa and DCFH is a method proposed to screen for chemical ROS production by NPs.     

Polystyrene nanoplastics affect growth and microcystin production of Microcystis aeruginosa

Nanoplastics are widely distributed in freshwater environments, but few studies have addressed their effects on freshwater algae, especially on harmful algae. In this study, the effects of polystyrene (PS) nanoplastics on Microcystis aeruginosa (M. aeruginosa) growth, as well as microcystin (MC) production and release, were investigated over the whole growth period. The results show that PS nanoplastics caused a dose-dependent inhibitory effect on M. aeruginosa growth and a dose-dependent increase in the aggregation rate peaking at 60.16% and 46.34%, respectively, when the PS nanoplastic concentration was 100 mg/L. This caused significant growth of M. aeruginosa with a specific growth rate up to 0.41 d^?1 (50 mg/L PS nanoplastics). After a brief period of rapid growth, the tested algal cells steadily grew. In addition, the increase in PS nanoplastics concentration promoted the production and release of MC. When the PS nanoplastic concentration was 100 mg/L, the content of the intracellular (intra-) and extracellular (extra-) MC increased to 199.1 and 166.5 μg/L, respectively, on day 26, which was 31.4% and 31.1% higher, respectively, than the control. Our results provide insights into the action mechanism of nanoplastics on harmful algae and the potential risks to freshwater environments.

     

Combined effect of polystyrene plastics and triphenyltin chloride on the green algae Chlorella pyrenoidosa

The combined effect of polystyrene (PS) particles and triphenyltin chloride (TPTCl) to the green algae Chlorella pyrenoidosa was studied. The 96 h IC₅₀ of TPTCl to the green algae C. pyrenoidosa was 30.64 μg/L. The toxicity of PS particles to C. pyrenoidosa was size-dependent, with the 96 h IC₅₀ at 9.10 mg/L for 0.55 μm PS but no toxicity observed for 5.0 μm PS. The exposure to 0.55 μm PS led to damage on structure of algal cells, which could in turn cause inhibition on photosynthesis and population growth of the green algae. TPTCl concentrations in test medium were lowered by 15–19% at presence of 0.55 μm PS particles, indicating a reduced bioavailability of TPTCl. In spite of this reduced bioavailability, the presence of PS increased the toxicity of TPTCl, which might be attributed to facilitated uptake of TPTCl by the green algae after the damage of cell structure. The overall results of the present study provided important information on the effect of PS on the bioavailability and toxicity of TPTCl to phytoplankton species.

     

Toxicity,uptake, and accumulation of nano and bulk cerium oxide particles in <Emphasis Type="Italic">Artemia salina</Emphasis>

Although the toxicological impact of metal oxide nanoparticles has been studied for the last few decades on aquatic organisms, the exact mechanism of action is still unclear. The fate, behavior, and biological activity of nanoparticles are dependent on physicochemical factors like size, shape, surface area, and stability in the medium. This study deals with the effect of nano and bulk CeO₂ particles on marine microcrustacean, Artemia salina. The primary size was found to be 15 ± 3.5 and 582 ± 50 nm for nano and bulk CeO₂ (TEM), respectively. The colloidal stability and sedimentation assays showed rapid aggregation of bulk particles in seawater. Both the sizes of CeO₂ particles inhibited the hatching rate of brine shrimp cyst. Nano CeO₂ was found to be more toxic to A. salina (48 h LC₅₀ 38.0 mg/L) when compared to bulk CeO₂ (48 h LC₅₀ 92.2 mg/L). Nano CeO₂-treated A. salina showed higher oxidative stress (ROS) than those treated with the bulk form. The reduction in the antioxidant activity indicated an increase in oxidative stress in the cells. Higher acetylcholinesterase activity (AChE) was observed upon exposure to nano and bulk CeO₂ particles. The uptake and accumulation of CeO₂ particles were increased with respect to the concentration and particle size. Thus, the above results revealed that nano CeO₂ was more lethal to A. salina as compared to bulk particles.     

纳米氧化铈对汽油发动机尾气污染物排放的影响

通过非水微乳液法制备了纳米氧化铈,并将之添加到90^#汽油中,研究了纳米氧化铈对汽油动力性能、尾气污染物CO、HC、PM、NOx排放的影响。结果表明：非水微乳液法制备的纳米氧化铈粒径在30～50nm之间,粒径分布较窄;添加浓度为100mg／L时,不会对汽油的动力性能产生明显影响,但可以明显降低90。汽油尾气中的CO、HC、PM、NOx排放。其中,800r／min的正常怠速下可以降低CO排放19．39％、HE排放19．92％、NOx排放51．19％、PM排放25％;在2000r／min的高怠速下可降低CO排放16．17％、NOx排放46．92％、PM排放16．67％。     

Assessment of nitrogen losses through nitrous oxide from abattoir wastewater-irrigated soils

The land disposal of waste and wastewater is a major source of N₂O emission. This is due to the presence of high concentrations of nitrogen (N) and carbon in the waste. Abattoir wastewater contains 186 mg/L of N and 30.4 mg/L of P. The equivalent of 3 kg of abattoir wastewater-irrigated soil was sieved and taken in a 4-L plastic container. Abattoir wastewater was used for irrigating the plants at the rates of 50 and 100 % field capacity (FC). Four crop species were used with no crop serving as a control. Nitrous oxide emission was monitored using a closed chamber technique. The chamber was placed inside the plastic container, and N₂O emission was measured for 7 days after the planting. A syringe and pre-evacuated vial were used for collecting the gas samples; a fresh and clean syringe was used each time to avoid cross-contamination. The collected gas samples were injected into a gas chromatography device immediately after each sampling to analyse the concentration of N₂O from different treatments. The overall N₂O emission was compared for all the crops under two different abattoir wastewater treatment rates (50 and 100 % FC). Under 100 % FC (wastewater irrigation), among the four species grown in the abattoir wastewater-irrigated soil, Medicago sativa (23 mg/pot), Sinapis alba (21 mg/pot), Zea mays (20 mg/pot) and Helianthus annuus (20 mg/pot) showed higher N₂O emission compared to the 50 % treatments—M. sativa (17 mg/pot), S. alba (17 mg/pot), Z. mays (18 mg/pot) and H. annuus (18 mg/pot). Similarly, pots with plants have shown 15 % less emission than the pots without plants. Similar trends of N₂O emission flux were observed between the irrigation period (4-week period) for 50 % FC and 100 % FC. Under the 100 % FC loading rate treatments, the highest N₂O emission was in the following order: week 1 > week 4 > week 3 > week 2. On the other hand, under the 50 % FC loading rate treatments, the highest N₂O emission was recorded in the first few weeks and in the following order: week 1 > week 2 > week 3 > week > 4. Since N₂O is a greenhouse gas with high global warming potential, its emission from wastewater irrigation is likely to impact global climate change. Therefore, it is important to examine the effects of abattoir wastewater irrigation on soil for N₂O emission potential.

     

Ecotoxicity of nanoparticles of CuO and ZnO in natural water

The acute toxicity of CuO and ZnO nanoparticles in artificial freshwater (AFW) and in natural waters to crustaceans Daphnia magna and Thamnocephalus platyurus and protozoan Tetrahymena thermophila was compared. The L(E)C₅₀ values of nanoCuO for both crustaceans in natural water ranged from 90 to 224 mg Cu/l and were about 10-fold lower than L(E)C₅₀ values of bulk CuO. In all test media, the L(E)C₅₀ values for both bulk and nanoZnO (1.1-16 mg Zn/l) were considerably lower than those of nanoCuO. The natural waters remarkably (up to 140-fold) decreased the toxicity of nanoCuO (but not that of nanoZnO) to crustaceans depending mainly on the concentration of dissolved organic carbon (DOC). The toxicity of both nanoCuO and nanoZnO was mostly due to the solubilised ions as determined by specific metal-sensing bacteria.     

Time-dependent degradation and toxicity of diclofop-methyl in algal suspensions

Background, aim, and scope  As emerging contaminants, transformation products of the pollutants via various environmental processes are rather unknown, and some may predominately contribute to the environmental risks of the parent compounds. Hence, studies on transformation products complement the assessment of the environmental safety of the parent compounds. In this study, degradation experiments and toxicity tests using diclofop-methyl (DM), a widely used herbicide, and selected major transformation products were carried out in algal cultures to assess the time course of DM toxicity and its relevance in the formation of new breakdown products. Methods  The alga Chlorella vulgaris was maintained in the algal growth medium HB IV. The inhibition of algal growth was determined by measuring optical density at 680 nm (OD₆₈₀). Initially, DM and two selected breakdown products were added to the algal cultures, and following degradation experiments analyses were carried out by high performance liquid chromatography. In addition, the possible relationship between DM degradation and toxicity was assessed, based on physico-chemical properties of the compounds and their toxicity. Results  DM was rapidly absorbed onto the surface of the algal cells where it was hydrolyzed to diclofop (DC). Further degradation to 4-(2, 4-dichlorophenoxy) phenol (DP) occurred in the cells. However, only a minor amount of DC was degraded to DP under the same conditions when DC was initially added to the algal culture. When C. vulgaris was exposed to these compounds for 96 h, the determined EC₅₀ showed that DC was about ten times less toxic than DM (EC₅₀ = 0.42 mg/L) and that DP (EC₅₀ = 0.20 mg/L) was the most toxic. Discussion  Due to strong hydrophobicity and rare dissociation, DM has tendency toward absorption as compared to DC. The higher average degradation rates of DC initially treated by DM revealed the damage of the cell membranes caused by the DM and, thus, enhanced movement of DC into the cells. Following occurrence of phenolic breakdown products, DP suggested that DC should be intracellularly degraded to DP, which had a more potent mode of action and a higher acute toxicity. Moreover, the results for EC₅₀ at various intervals were in accordance with degradation processes of the initial compounds, in which rapid formation of DP was attributed to an increasing toxicity of DM. Conclusions  The toxicity of DM in algal suspensions increased with time due to its degradation to DP, which contributed significantly to the determined toxicity. These results indicate that the toxicity of the pesticide probably depends significantly on degradation. It is thus important to consider the time-dependent environmental processes when evaluating the toxicological effects of pesticides for proper risk assessment. Recommendations and perspectives  Increasing transformation products of these contaminants are identified in the environment, although they seem to be unknown in terms of the lacking studies on environmental behavior and ecotoxicity concerning them. Certain breakdown products probably greatly contribute to the apparent toxicity of the parent compounds, which is ascribed to the parent compounds in general studies ignoring the dependence of their toxicity on various transformation pathways. These studies that identify new intermediates and assess their toxicity via the environmental processes will be helpful to distinguish the nature of toxicity of the parent contaminants.     

Toxicity of two types of silver nanoparticles to aquatic crustaceans Daphnia magna and Thamnocephalus platyurus

Although silver nanoparticles (NPs) are increasingly used in various consumer products and produced in industrial scale, information on harmful effects of nanosilver to environmentally relevant organisms is still scarce. This paper studies the adverse effects of silver NPs to two aquatic crustaceans, Daphnia magna and Thamnocephalus platyurus. For that, silver NPs were synthesized where Ag is covalently attached to poly(vinylpyrrolidone) (PVP). In parallel, the toxicity of collargol (protein-coated nanosilver) and AgNO₃ was analyzed. Both types of silver NPs were highly toxic to both crustaceans: the EC50 values in artificial freshwater were 15–17 ppb for D. magna and 20–27 ppb for T. platyurus. The natural water (five different waters with dissolved organic carbon from 5 to 35 mg C/L were studied) mitigated the toxic effect of studied silver compounds up to 8-fold compared with artificial freshwater. The toxicity of silver NPs in all test media was up to 10-fold lower than that of soluble silver salt, AgNO₃. The pattern of the toxic response of both crustacean species to the silver compounds was almost similar in artificial freshwater and in natural waters. The chronic 21-day toxicity of silver NPs to D. magna in natural water was at the part-per-billion level, and adult mortality was more sensitive toxicity test endpoint than the reproduction (the number of offspring per adult).     

Effects of suspended solids on cyanobacterial bloom formation under different wind fields

Wind waves and suspended solids (SS) generated by the resuspension of sediments are ubiquitous characteristics of lake ecosystems. However, their effects on phytoplankton remain poorly elucidated in shallow eutrophic lakes. Laboratory experiments were carried out to investigate the responses of Microcystis aeruginosa to SS under static (wind speed of 0 m/s) and breeze (wind speed of 3 m/s) conditions. Results showed that 50 mg/L SS can promote the growth of M. aeruginosa, accelerate the formation of colonies, and increase the floating rate under no-wind conditions. Comparing with static environment, breeze can significantly increase the growth rate of M. aeruginosa and benefit the formation of larger colonies of algae cells. Driven by wind and SS, the buoyancy of the cyanobacteria community in different experimental groups was obviously different. The specific performance was that low SS concentration and breeze were in favor of the floating of cyanobacteria, while high SS concentration went against the floating of algal cells. As a conclusion, wind speed of 3 m/s and 20–50 mg/L SS have a synergistic effect on the formation of cyanobacterial blooms. This study can provide an improved current understanding of bloom formation and turbidity management strategies in shallow eutrophic lakes.

     

Accumulation of free and covalently bound microcystins in tissues of Lymnaea stagnalis (Gastropoda) following toxic cyanobacteria or dissolved microcystin-LR exposure

Accumulation of free microcystins (MCs) in freshwater gastropods has been demonstrated but accumulation of MCs covalently bound to tissues has never been considered so far. Here, we follow the accumulation of total (free and bound) MCs in Lymnaea stagnalis exposed to i) dissolved MC-LR (33 and 100 μg L⁻¹) and ii) Planktothrix agardhii suspensions producing 5 and 33 μg MC-LR equivalents L⁻¹ over a 5-week period, and after a 3-week depuration period. Snails exposed to dissolved MC-LR accumulated up to 0.26 μg total MCs g⁻¹ dry weight (DW), with no detection of bound MCs. Snails exposed to MCs producing P. agardhii accumulated up to 69.9 μg total MCs g⁻¹ DW, of which from 17.7 to 66.7% were bound. After depuration, up to 15.3 μg g⁻¹ DW of bound MCs were detected in snails previously exposed to toxic cyanobacteria, representing a potential source of MCs transfer through the food web.     

Foliar use of TiO2-nanoparticles for okra (Abelmoschus esculentus L. Moench) cultivation on sewage sludge–amended soils: biochemical response and heavy metal accumulation

Considering its richness in organic and inorganic mineral nutrients, the recycling of sewage sludge (SS) is highly considered as a soil supplement in agriculture. However, the fate of hazardous heavy metal accumulation in the crops cultivated in SS amended soils is always a source of concern. Since nanoparticles are widely recognized to reduce heavy metal uptake by crop plants; thus, the present experiment deals with okra (Abelmoschus esculentus L. Moench) cultivation under the combined application of SS and TiO₂-nanoparticles (NPs). Triplicated pot experiments were conducted using different doses of SS and TiO₂-NPs such as 0 g/kg SS (control), 50 g/kg SS, 50 g/kg SS?+?TiO₂, 100 g/kg SS, and 100 g/kg SS?+?TiO₂, respectively. The findings of this study indicated that among the doses of treatment combinations investigated, 100 g/kg SS?+?TiO₂ showed a significant (p?<?0.05) increase in the okra plant yield (287.87?±?4.06 g/plant) and other biochemical parameters such as fruit length (13.97?±?0.54 cm), plant height (75.05?±?3.18 cm), superoxide dismutase (SOD: 110.68?±?3.11 μ/mg), catalase (CAT: 81.32?±?3.52 μ/mg), and chlorophyll content (3.12?±?0.05 mg/g fwt.). Also, the maximum contents of six heavy metals in the soil and cultivated okra plant tissues (fruit, stem, and root regions) followed the order of Fe?>?Mn?>?Cu?>?Zn?>?Cr?>?Cd using the same treatment. Bioaccumulation and health risk assessment indicated that foliar application of TiO₂-NPs significantly reduced the fate of heavy metal accumulation under higher doses of SS application. Therefore, the findings of this study suggested that the combined use of SS and TiO₂-NPs may be useful in ameliorating the negative consequences of heavy metal accumulation in cultivated okra crops.

     

Facile fabrication of green nano pure CeO2 and Mn-decorated CeO2 with Cassia angustifolia seed extract in water refinement by optimal photodegradation kinetics of malachite green

To eradicate the aquatic pollution caused by dyes, trendily the global researchers provide dedication to dye degradation using nanostructured photocatalyst. This research work is dedicated to explore an advanced, facile, bio-compact green fabricated nanostructure for water refinement. In this regard, plant-mediated syntheses of pure CeO₂ and Mn-decorated CeO₂ nano-powders have been inspected using seed extract of Cassia angustifolia. Investigations through UV-diffuse reflectance spectroscopy explored the significantly tuned band gap of Mn:CeO₂. FT-IR spectroscopy shows the existing functional groups of high-potential phenolic compounds, proteins, and amino acids in Cassia angustifolia act as reducing and capping agents involved in the green fabricated nanostructured samples. X-ray diffraction pattern has been exposed to crystalline cubic fluorite morphology in a single phase and it leads to a regulated optimized amount of Mn on CeO₂ nanostructure. The FESEM analysis predicts the morphology of CeO₂ in spherical and Mn:CeO₂ in flower-like structure. The HRTEM analysis has portrayed particle size of CeO₂ is 11 nm and tuned Mn:CeO₂ nanostructure is 9 nm. The HRTEM images revealed the average particle size in the range 10–12 nm in CeO₂ and 8–9 nm in 5 mol% Mn:CeO₂ nanoparticles. It showed a decrease in average particle size with an increase in Mn concentration and the reduction in size may be due to the replacement of Ce(IV) with Mn(II) ions. The elemental composition in nanostructure was predicted using energy-dispersive X-ray analysis. The rapid photocatalytic degradation efficiency of malachite green was effectually performed and compared with the kinetics model of Mn:CeO₂ and pure CeO₂ nanostructures. From the augmented results, tuned Mn:CeO₂ was found to act as the finest green fabricated photocatalyst in the amputation of lethal and carcinogenic dye.

     

Aggregation and ecotoxicity of CeO₂ nanoparticles in synthetic and natural waters with variable pH, organic matter concentration and ionic strength

The influence of pH (6.0-9.0), natural organic matter (NOM) (0-10 mg C/L) and ionic strength (IS) (1.7-40 mM) on 14 nm CeO₂ NP aggregation and ecotoxicity towards the alga Pseudokirchneriella subcapitata was assessed following a central composite design. Mean NP aggregate sizes ranged between 200 and 10000 nm. Increasing pH and IS enhanced aggregation, while increasing NOM decreased mean aggregate sizes. The 48 h-E_rC20s ranged between 4.7 and 395.8 mg CeO₂/L. An equation for predicting the 48 h-E_rC20 (48 h-E_rC20 = −1626.4 × (pH) + 109.45 × (pH)² + 116.49 × ([NOM]) − 14.317 × (pH) × ([NOM]) + 6007.2) was developed. In a validation study with natural waters the predicted 48 h-E_rC20 was a factor 1.08-2.57 lower compared to the experimental values.     

Eutrophication of Lake Tasaul, Romania—proposals for rehabilitation

Lake Tasaul on the Black Sea coast is highly eutrophic, but not strongly contaminated (heavy metals, PAHs, and organochlorine pesticides). Cyanophytes dominate phytoplankton by 67–94% and form frequent algal blooms. High primary production (up to 270 mg C_ass/m².h) and algal biomass (maximum chlorophyll a concentration 417 μg/l) may be controlled by light, as Secchi depth is often below 1 m. The main tributary, Casimcea River, provides high quantities of suspended matter and about 3 tons TP/year and 660 tons TN/year. Based on chemical and biological analysis as well as fishery investigations, we provide recommendations for Lake Tasaul rehabilitation.     

Identification of a phytotoxic photo-transformation product of diclofenac using effect-directed analysis

The pharmaceutical diclofenac (DCF) is released in considerably high amounts to the aquatic environment. Photo-transformation of DCF was reported as the main degradation pathway in surface waters and was found to produce metabolites with enhanced toxicity to the green algae Scenedesmus vacuolatus. We identified and subsequently confirmed 2-[2-(chlorophenyl)amino]benzaldehyde (CPAB) as a transformation product with enhanced toxicity using effect-directed analysis. The EC₅₀ of CPAB (4.8 mg/L) was a factor of 10 lower than that for DCF (48.1 mg/L), due to the higher hydrophobicity of CPAB (log K_ow = 3.62) compared with DCF (log D_ow = 2.04) at pH 7.0.     

Acute toxicity of 353-nonylphenol and its metabolites for zebrafish embryos

Background, aim and scope  Nonylphenol (NP) can be detected in the aquatic environment all over the world. It is applied as a technical mixture of isomers of which 353-NP is the most relevant both in terms of abundance (about 20% of total mass) and endocrine potential. 353-NP is metabolised in sewage sludge. The aims of the present study were to determine and to compare the acute toxicity of t-NP, 353-NP and its metabolites as well as to discuss if the toxicity of 353-NP changes during degradation. Materials and methods  353-NP and two of its metabolites were synthesised. The zebrafish embryo test was performed according to standard protocols. Several lethal and non-lethal endpoints during embryonal development were reported. NOEL, LOEL and EC₅₀ were calculated. Results  All tested compounds caused lethal as well as non-lethal malformations during embryo development. 353-NP showed a higher toxicity (EC₅₀ for lethal endpoints 6.7 mg/L) compared to its metabolites 4-(3.5-dimethyl-3-heptyl)-2-nitrophenol (EC₅₀ 13.3 mg/L) and 4-(3,5-dimethyl-3-heptyl)-2-bromophenol (EC₅₀ 27.1 mg/L). Discussion  In surface water, concentrations of NP are far below the NOEC identified by the zebrafish embryo test. However, in soils and sewage sludge, concentrations may reach or even exceed these concentrations. Therefore, sludge-treated sites close to surface waters should be analysed for NP and its metabolites in order to detect an unduly high contamination due to runoff events. Conclusions  The results of the present study point out that the toxicity of 353-NP probably declines during metabolisation in water, sediment and soil, but does not vanish since the major metabolites exhibit a clear toxic potential for zebrafish embryos. Recommendations and perspectives  Metabolites of environmental pollutants should be included in the ecotoxicological test strategy for a proper risk assessment. An erratum to this article can be found at     

Silver nanoparticles from Tabernaemontana divaricate leaf extract: mechanism of action and bio-application for photo degradation of 4-aminopyridine

Silver nanoparticles (Ag NPs) were synthesised by the reduction of Ag⁺ to Ag⁰ in the presence of enol form of flavonoids present in plant extract of Tabernaemontana divaricate (T. divaricate). Prepared Ag NPs were characterised using UV–Vis, XRD, HR-TEM with EDX and XPS techniques. XPS spectra exhibited peaks at 366 eV and 373 eV, which specified spin orbits for Ag 3d_3/2, and Ag 3d_5/2 that confirmed the formation of Ag NPs. Ag NPs were spherical in shape with an average size of 30 nm as revealed by HR-TEM and FE-SEM techniques. EDX studies verified the high purity of Ag NPs with silver 46.96%, carbon 16.35%, oxygen 16.22%, nitrogen 20.25% and sulphur 0.21%. LC–MS analysis of plant extract confirmed the qualitative presence of alkaloids, tannins, flavonoids, phenols, and carbohydrates. Prepared Ag NPs showed good photocatalytic activity towards degradation of 4-Amniopyridine with 61% degradation efficiency at optimum conditions in 2 h of reaction time under visible light. The ten intermediates were found within the mass number of 0–450. Ag NPs synthesised using bio-extract have also shown good inactivation against Escherichia coli (E. coli) and Bacillus subtilis (B. subtilis) bacteria due to the availability of free radicals.

Graphical abstract

     

Hydrous ferric oxide nanoparticles hosted porous polyethersulfone adsorptive membrane: chromium (VI) adsorptive studies and its applicability for water/wastewater treatment

In this present study, adsorptive membranes for Cr(VI) ion removal were prepared by blending polyethersulfone (PES) with hydrous ferric oxide (HFO) nanoparticles (NPs). The effects of HFO NPs to PES weight ratio (0–1.5) on the physicochemical properties of the resultant HFO/PES adsorptive membranes were investigated with respect to the surface chemistry and roughness as well as structural morphologies using different analytical instruments. The adsorptive performance of the HFO NPs/PES membranes was studied via batch adsorption experiments under various conditions by varying solution pH, initial concentration of Cr(VI), and contact time. The results showed that the membrane made of HFO/PES at a weight ratio of 1.0 exhibited the highest adsorption capacity which is 13.5 mg/g. Isotherm and kinetic studies revealed that the mechanism is best fitted to the Langmuir model and pseudo-second-order model. For filtration of Cr(VI), the best promising membranes showed improved water flux (629.3 L/m² h) with Cr(VI) ion removal of 75%. More importantly, the newly developed membrane maintained the Cr(VI) concentration below the maximum contamination level (MCL) for up to 9 h.