Search Results (21)

A stabilized biochar (BC)–nano-scale zero-valent iron (nZVI) composite (BC-nZVI@Cell-g-PAA) was prepared using cellulose-grafted polyacrylic acid (Cell-g-PAA) as the raw material through in situ polymerization and liquid-phase reduction methods for the remediation of hexavalent chromium (Cr(VI))-contaminated water. BC-nZVI@Cell-g-PAA was characterized by XRD, FT-IR, SEM, BET, TEM, and XPS. According to the batch experiments, under optimized conditions (Cr(VI) concentration of 50 mg/L, pH = 3, and dosage of 2 g/L), the BC-nZVI@Cell-g-PAA composite achieved maximum Cr(VI) removal efficiency (99.69%) within 120 min. Notably, BC, as a carrier, achieved a high dispersion of nZVI through its porous structure, effectively preventing particle agglomeration and improving reaction activity. Simultaneously, the functional groups on the surface of Cell-g-PAA provided excellent protection for nZVI, significantly suppressing its oxidative deactivation. Furthermore, the composite effectively reduced Cr(VI) to insoluble trivalent chromium(Cr(III)) species and stabilized them on its surface through immobilization. The synergistic effects of physical adsorption and chemical reduction greatly contributed to the removal efficiency of Cr(VI). Remarkably, the composite exhibited excellent reusability with a removal efficiency of 62.4% after five cycles, demonstrating its potential as a promising material for remediating Cr(VI)-contaminated water. In conclusion, the BC-nZVI@Cell-g-PAA composite not only demonstrated remarkable efficiency in Cr(VI) removal but also showcased its potential for practical applications in environmental remediation, as evidenced by its sustained performance over multiple reuse cycles. Moreover, Cr(VI), a toxic and carcinogenic substance, poses significant risks to aquatic ecosystems and human health, underscoring the importance of developing effective methods for its removal from contaminated water. Full article

The disinfection of drinking water is essential for eliminating pathogens and preventing waterborne diseases. However, this process generates various disinfection byproducts (DBPs), which toxicological research indicates can have detrimental effects on living organisms. Moreover, the safety of these DBPs has not been sufficiently assessed, underscoring the need for a comprehensive evaluation of their toxic effects and associated health risks. Compared to traditional methods for studying the toxicity of pollutants, emerging electrochemical sensing technologies offer advantages such as simplicity, speed, and sensitivity, presenting an effective means for toxicity research on pollutants. However, challenges remain in this field, including the need to improve electrode sensitivity and reduce electrode costs. In this study, a pencil graphite electrode (PGE) was modified with carboxylated multi-walled carbon nanotubes (MWCNT-COOH) and nano-iron (III) oxide (α-Fe₂O₃) to fabricate a low-cost electrode with excellent electrocatalytic performance for cell-active substances. Subsequently, a novel cellular electrochemical sensor was constructed for the sensitive detection of the toxicity of three drinking water DBPs. The half inhibitory concentration (IC₅₀) values of 2-chlorophenylacetonitrile (2-CPAN), 3-chlorophenylacetonitrile (3-CPAN), and 4-chlorophenylacetonitrile (4-CPAN) for HepG2 cells were 660.69, 831.76, and 812.83 µM, respectively. This study provides technical support and scientific evidence for the toxicity detection and safety assessment of emerging contaminants. Full article

Arsenic contamination of water endangers the health of millions of people worldwide, affecting certain countries and regions with especial severity. Interest in the use of Fe-based metal organic frameworks (MOFs) to remove inorganic arsenic species has increased due to their stability and adsorptive properties. In this study, the performance of a synthesized Nano-{Fe-BTC} MOF, containing iron oxide octahedral chains connected by trimesic acid linkers, in adsorbing As(III) and As(V) species was investigated and compared with commercial Basolite^®F300 MOF. Despite their similarities in composition, they exhibit distinct structural characteristics in their porosity, pore size, and surface areas, which affected the adsorption processes. The kinetic data of the adsorption of As(III) and As(V) by both Fe-MOFs fitted the pseudo second-order model well, with the kinetic constant being higher for Basolite^®F300 given its higher porosity. Intraparticle diffusion was, in both cases, the rate controlling step with the contribution of film diffusion in the adsorption processes, which achieved equilibrium after 1 h. The maximum adsorption capacity for As(V), 41.66 mg g⁻¹, was obtained with Basolite^®F300 at the 6.5–10 pH range, whereas Nano-{Fe-BTC} showed a different behaviour as maximum adsorption (14.99 mg g⁻¹) was obtained at pH 2. However, both adsorbents exhibited the same performance for As(III) adsorption, which is not adsorbed at pH < 9. The Langmuir adsorption isotherm model fitted well for As(III) and As(V) adsorption by Nano-{Fe-BTC} and As(III) by Basolite^®F300, whereas the Freundlich model fitted best for As(V) given its superior structural properties. Full article

Late-onset Alzheimer’s disease (LOAD) is a chronic, multifactorial, and progressive neurodegenerative disease that associates with aging and is highly prevalent in our older population (≥65 years of age). This hypothesis generating this narrative review will examine the important role for the use of sodium thiosulfate (STS) as a possible multi-targeting treatment option for LOAD. Sulfur is widely available in our environment and is responsible for forming organosulfur compounds that are known to be associated with a wide range of biological activities in the brain. STS is known to have (i) antioxidant and (ii) anti-inflammatory properties; (iii) chelation properties for calcium and the pro-oxidative cation metals such as iron and copper; (iv) donor properties for hydrogen sulfide production; (v) possible restorative properties for brain endothelial-cell-derived bioavailable nitric oxide. Thus, it becomes apparent that STS has the potential for neuroprotection and neuromodulation and may allow for an attenuation of the progressive nature of neurodegeneration and impaired cognition in LOAD. STS has been successfully used to prevent cisplatin oxidative-stress-induced ototoxicity in the treatment of head and neck and solid cancers, cyanide and arsenic poisoning, and fungal skin diseases. Most recently, intravenous STS has become part of the treatment plan for calciphylaxis globally due to vascular calcification and ischemia-induced skin necrosis and ulceration. Side effects have been minimal with reports of metabolic acidosis and increased anion gap; as with any drug treatment, there is also the possibility of allergic reactions, possible long-term osteoporosis from animal studies to date, and minor side-effects of nausea, headache, and rhinorrhea if infused too rapidly. While STS poorly penetrates the intact blood–brain barrier(s) (BBBs), it could readily penetrate BBBs that are dysfunctional and disrupted to deliver its neuroprotective and neuromodulating effects in addition to its ability to penetrate the blood–cerebrospinal fluid barrier of the choroid plexus. Novel strategies such as the future use of nano-technology may be helpful in allowing an increased entry of STS into the brain. Full article

Polycyclic aromatic hydrocarbons (PAHs) and arsenic (As) are common pollutants co-existing in the environment, causing potential hazards to the ecosystem and human health. How their behaviors are affected by micro/nano particles in the environment are still not very clear. Through a series of static adsorption experiments, this study investigated the adsorption of pyrene and arsenite (As (III)) using micro/nano carbon black and iron oxide under different conditions. The objectives were to determine the kinetics and isotherms of the adsorption of pyrene and As (III) using micro/nano carbon black and iron oxide and evaluate the impact of co-existing conditions on the adsorption. The microstructure of micro/nano carbon black (C 94.03%) is spherical-like, with a diameter of 100–200 nm. The micro/nano iron oxide (hematite) has irregular rod-shaped structures, mostly about 1 µm long and 100–200 nm wide. The results show that the micro/nano black carbon easily adsorbed the pyrene, with a pseudo-second-order rate constant of 0.016 mg/(g·h) and an adsorption capacity of 283.23 μg/g at 24 h. The micro/nano iron oxide easily adsorbed As (III), with a pseudo-second-order rate constant of 0.814 mg/(g·h) and an adsorption capacity of 3.45 mg/g at 24 h. The mechanisms of adsorption were mainly chemical reactions. Micro/nano carbon black hardly adsorbed As (III), but its adsorption capability for pyrene was reduced by the presence of As (III), and this effect increased with an increase in the As (III) concentration. The adsorbed pyrene on the micro/nano black carbon could hardly be desorbed. On the other hand, the micro/nano iron oxide could hardly adsorb the pyrene, but its adsorption capability for As (III) was increased by the presence of pyrene, and this effect increased with an increase in the pyrene concentration. The results of this study provide guidance for the risk management and remediation of the environment when there is combined pollution of PAHs and As. Full article

Natural limonite, which contains mainly nano-sized iron and manganese oxides, is widely distributed worldwide. This study investigated the kinetics, thermodynamics, and the effects of pH, ion strength, and anions on the adsorption of Sb(III) via limonites sampled from Xinqiao and Yeshan (Tongling, China). Results show that adsorption equilibrium is achieved after 24 h for all experiments. Under initial Sb(III) = 200 mg/L, pH = 3.0, and temperature = 25 °C, Sb adsorption quantities for X1 (Mn-free limonite from Xinqiao), X2 (Mn-containing limonite from Xinqiao), Y1 (Mn-free limonite from Yeshan), and Y2 (Mn-containing limonite from Yeshan) are 10.92, 12.97, 27.12, and 89.34 mg/g, respectively. Manganese oxides in limonites promote Sb removal through oxidizing Sb(III) to Sb(V). The adsorption processes for all four limonites are fitted with a pseudo-second-order model. All adsorptions except for X1 fit with the Freundlich model; for X1, the Langmuir adsorption model is better. All adsorptions are spontaneous reactions (ΔG < 0). All adsorptions except for Y1 (ΔH < 0, exothermic reaction) are endothermic reactions (ΔH > 0). Antimony adsorption is independent of solution pH for Mn-free limonites but is negatively related to solution pH for Mn-containing limonites. Generally, ion strength has a weak positive effect on Sb adsorption. The effects of anions on Sb adsorption are grouped into three types: weak negative (NO₃⁻ and SO₄²⁻), negative (CO₃²⁻, SiO₄⁴⁻, and PO₄³⁻), and equivocal (humic acid). This study indicates that due to a much higher surface area, Yeshan (124.8 m²/g for X1 and 171.7 m²/g for X2) rather than Xinqiao (13.7 m²/g for Y1 and 12.8 m²/g for Y2) limonites are better materials for Sb(III) removal in an aqueous solution. The key factors for the better use of limonite as an Sb(III) treatment material include temperature, pH, ion strength, and Mn content. Full article

Due to their unique properties, iron nanoparticles find diverse applications across various fields, including catalysis, electronics, wastewater treatment, and energy storage. Nano-iron particles are mostly sub-micrometer particles that are highly reactive to both air (oxygen) and water, and in nanoparticles (size below 100 nm), it is even more rapid than the bulk material. This characteristic limits its use in inert environments. Iron nanoparticles are not toxic and are mostly used for wastewater treatment. Understanding the hydrogen reduction mechanisms and conditions that lead to the formation of metallic iron particles from iron (III)-nitrate from an aerosol is crucial for enabling their effective utilization. In this work, we studied the hydrogen reduction behavior of Fe₂O₃ in the absence and presence of additives (SiO₂ or Pt). The particles were prepared via ultrasonic spray pyrolysis and hydrogen reduction. The characterization was performed with a scanning electron microscope, energy-dispersive X-ray spectroscopy, and X-ray diffraction. In the absence of additives, the oxygen content of iron oxide particles decreased with increasing temperature from 700 to 950 °C but significantly increased with the doping of 10 mL (40 wt.%) of SiO₂. The inhibitory effect of Si on the hydrogen reduction of Fe₂O₃ formed was more pronounced at 950 °C than at 700 °C. In contrast, the doping of only 5 mL (15 wt.%) of Pt significantly decreased the oxygen concentration in the synthesized particles by catalyzing the reduction reaction of iron oxides at 700 °C. The metallic iron (Fe) product, obtained in the undoped iron oxides run at only 950 °C, was also formed at 700 °C in the Pt-doped Fe₂O₃ run. Full article

Micro electro-mechanical systems (MEMS) combining sensing and microfluidics functionalities, as are common in Lab-on-Chip (LoC) devices, are increasingly based on polymers. Benefits of polymers include tunable material properties, the possibility of surface functionalization, compatibility with many micro and nano patterning techniques, and optical transparency. Often, additional materials, such as metals, ceramics, or silicon, are needed for functional or auxiliary purposes, e.g., as electrodes. Hybrid patterning and integration of material composites require an increasing range of fabrication approaches, which must often be newly developed or at least adapted and optimized. Here, a microfabrication process concept is developed that allows one to implement attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) and electrochemistry on an LoC device. It is designed to spatially resolve chemical sensitivity and selectivity, which are instrumental for the detection of chemical distributions, e.g., during on-flow chemical and biological reaction chemistry. The processing sequence involves (i) direct-write and soft-contact UV lithography in SUEX dry resist and replication in polydimethylsiloxane (PDMS) elastomers as the fluidic structure; (ii) surface functionalization of PDMS with oxygen plasma, 3-aminopropyl-triethoxysilane (APTES), and a UV-curable glue (NOA 73) for bonding the fluidic structure to the substrate; (iii) double-sided patterning of silicon nitride-coated silicon wafers serving as the ATR-FTIR-active internal reflection element (IRE) on one side and the electrode-covered substrate for microfluidics on the back side with lift-off and sputter-based patterning of gold electrodes; and (iv) a custom-designed active vacuum positioning and alignment setup. Fluidic channels of 100 μm height and 600 μm width in 5 mm thick PDMS were fabricated on 2” and 4” demonstrators. Electrochemistry on-chip functionality was demonstrated by cyclic voltammetry (CV) of redox reactions involving iron cyanides in different oxidation states. Further, ATR-FTIR measurements of laminar co-flows of H₂O and D₂O demonstrated the chemical mapping capabilities of the modular fabrication concept of the LoC devices. Full article

The development of modern photovoltaic thermal systems (PV/T) is one of the most important steps in the application of using solar energy to produce both electricity and heat. Studies have shown that a system consisting of a heat-collecting tank the is most efficient system, in which the phase change materials (PCMs) are mixed with nanoparticles inside the system that are cooled by a cooling fluid (preferably a nanofluid). The PCMs have a high capacity to store energy in the form of latent heat. Nanoparticles are added to PCMs to treat and improve the low thermal conductivity of these materials. In this experimental study, nano-iron oxide III (Fe₂O₃) was added to paraffin wax in multiple mass fractions to evaluate the thermophysical changes that can be occur on the wax properties. Four samples of paraffin–nano-Fe₂O₃ were prepared with mass fractions of 0.5%, 1%, 2% and 3%, and their thermophysical properties were compared with pure paraffin (without nano additives). The results from this study showed that adding nano-Fe₂O₃ at any mass fraction increases the viscosity and density of the product. Thermal conductivity is improved by adding nano-Fe₂O₃ to paraffin wax by 10.04%, 57.14%, 76.19%, and 78.57% when adding mass fractions of 0.5%, 1%, 2%, and 3%, respectively. Stability tests showed that the prepared samples have excellent thermal stability (especially for 0.5% and 1% added nano-Fe₂O₃) to acceptable level of stability when adding 3% of nano-Fe₂O₃. The nano-Fe₂O₃ paraffin PV/T system was tested outdoors to ensure its ability to operate in the harshest weather conditions of Baghdad city. The current experimental results indicated clear evidence of the success of the examined nano-PCM. Full article

Dye adsorption by magnetic modified biochar has now received growing interest due to its excellent adsorption performance and facile separation for recycling. In this study, nano iron oxide–modified biochar was fabricated via the successive hydrothermal-pyrolyzing method using Chlorella vulgaris (Cv) and FeSO₄·7H₂O as raw materials, and its adsorption on Rhodamine B (RhB) in aqueous solution was studied. Multiple techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET), vibrating sample magnetometry (VSM) and X-ray photoelectron spectroscopy (XPS) were employed to comprehensively characterize the structure, morphology and physicochemical properties of the adsorbent. The as-synthesized nano iron oxide–modified biochar (CBC-Fe(II)) exhibited a large surface area (527.6 m²/g) and high magnetic saturation value (13.7 emu/g) to facilitate magnetic separation. Compared with CBC and CBC-Fe(III), CBC-Fe(II) exhibited superior adsorption ability towards RhB in aqueous solution, with a maximum adsorption capacity of 286.4 mg/g. The adsorption process of RhB onto CBC-Fe(II) was well described by the pseudo-second-order kinetic model and Langmuir isotherm model, indicating monolayer chemisorption behaviors for the adsorption system. Facile preparation, great adsorption performance and magnetic recovery properties endow CBC-Fe(II) to be a promising adsorbent for dye removal. Full article

P-nitrophenol (PNP), a highly toxic carcinogen, is very stable due to its benzene structure. Advanced oxidation technology is becoming the main means for degrading it. A nano iron-cobalt (Co-nZVI) catalyst, supported by granular activated carbon (GAC), was prepared using liquid-phase reduction, and sodium persulfate’s (PS’s) potential to degrade PNP was studied. The Co-nZVI/GAC nanocomposites were classified, and effects of PS dosage, Co-nZVI/GAC dosage, material system type, PNP concentration, initial pH, and material reuse rate on the reaction were investigated. Activated carbon successfully supported iron and cobalt. At 1 mmol/L of PS, the maximum PNP degradation rate was 99.19%, which was unachievable at other dosages. With only Co-nZVI/GAC present, the rate was 69.8%; with activated persulfate present, it increased to 99.19%. The activated PS system was relatively stable under acidic conditions. Catalysis was induced by adding Co-nZVI/GAC (1.5 g/L). When added four times, the catalytic rate was 57%. Liquid chromatography–mass spectrometry (LC-MS) showed that PNP degradation involves the transfer of PNP to p-benzoquinone (PBQ), the main activators being iron(II) and iron(III) and the key active substances being sulfate (SO₄²⁻) and hydroxide (·OH). In conclusion, Co-nZVI/GAC-activated PS effectively removes PNP. Full article

Recently, large-scale agriculture has led to increasing crop production. To increase crop productivity in large-scale cropping systems, attempts have been made to make nano-fertilizers and deliver them to the crops by extension of nanotechnology. Hence, nano-fertilizers might be defined as nanoparticles that may directly assist in supplying essential nutrients for crop productivity. Seed germination is the first and the most susceptible stage in the plant’s growing phases, so could be considered as an index to evaluate the effect of newly developed materials such as nanoparticles (NPs), providing useful information for researchers. In our experiments, germination tests have been carried out in Petri dishes containing wet filter paper and nano-primed seeds. We had biosynthesized seven nanoparticles in our previous studies including calcinated and non-calcinated zinc oxide, zinc, magnesium oxide, silver, copper, and iron nanoparticles. The effect of these biogenic nanoparticles and their counterpart metallic salts including zinc acetate, magnesium sulfate, silver nitrate, copper sulfate, and iron (III) chloride was studied on two popularly grown plants, wheat and flax, in laboratory conditions to obtain preliminary information for future field experiments. Germination percentage, shoot length, root length, seedlings length, root–shoot ratio, seedling vigor index (SVI), shoot length stress tolerance index (SLSI), and root length stress tolerance index (RLSI) were calculated on the second and seventh days of the experiment. According to the results, the response of the plants to metal containing nanoparticles and metal salts mainly depend on the type of the metal, plant species, concentration of the NP suspension or salt solution, condition of the exposure, and the stage of growth. Full article

This work reports the fabrication of iron oxide mesoporous magnetic nanostructures (IO-MMNs) via the nano-replication method using acid-prepared mesoporous spheres (APMS) as the rigid silica host and iron (III) nitrate as the iron precursor. The obtained nanosized mesostructures were fully characterized by SEM, TEM, DLS, FTIR, XRD, VSM, and nitrogen physisorption. IO-MMNs exhibited relatively high surface areas and large pore volumes (S_BET = 70–120 m²/g and V_pore = 0.25–0.45 cm³/g), small sizes (~300 nm), good crystallinity and magnetization, and excellent biocompatibility. With their intrinsic porosities, high drug loading efficiencies (up to 70%) were achieved and the drug release rates were found to be pH-dependent. Cytotoxicity, confocal microscopy, and flow cytometry experiments against different types of cancerous cells indicated that Dox-loaded IO-MMNs reduced the viability of metastatic MCF-7 and KAIMRC-1 breast as well as HT-29 colon cancer cells, with the least uptake and toxicity towards normal primary cells (up to 4-fold enhancement). These results strongly suggest the potential use of IO-MMNs as promising agents for enhanced and effective drug delivery in cancer theranostics. Full article

Nanotechnology has received much attention in treating contaminated waters. In the present study, a facile co-precipitation method was employed to synthesize a novel iron and magnesium based binary metal oxide using a stoichiometrically fixed amount of FeNO₃·9H₂O and MgNO₃·6H₂O in a proportion of molar concentration 1:1 and was later evaluated in removing As (III) from contaminated waters. Characterization of the prepared nanomaterial was done using X-ray diffraction (XRD), scanning electron microscopy (SEM), Energy Dispersive X-ray Analysis (EDAX) and ultraviolet–visible spectrophotometry (UV-VIS). Experimental studies on batch scale were carried out, examining the effect of varying initial concentrations of metal, adsorbent dosage, application time and initial pH on removal efficiency. Arsenic removal increased on increasing adsorbent dosage (0.1–1 g/L) but trend reversed on increasing initial arsenic concentration attaining q_max of 263.20 mg/g. Adsorption was quite efficient in pH range 4–8. Freundlich fitted better for adsorption isotherm along with following Pseudo-2nd order kinetics. The reusability and effect of co-existing ions on arsenic adsorption, namely SO₄²⁻, CO₃²⁻ and PO₄³⁻ were also explored with reusability in 1st and 2nd cycles attained adsorptive removal up to 77% and 64% respectively. The prepared nano-adsorbent showed promising results in terms of high arsenic uptake (q_max of 263.20 mg/g) along with facile and cost-effective synthesis. Thus, the co-precipitation technique used in this work is a simple one step procedure without any use of any precursor as compared to most of the other procedures used for synthesis. Full article

Many investigations are currently being performed to develop the effective synthesis methodology of magnetic nanoparticles with appropriately functionalized surfaces. Here, the novelty of the presented work involves the preparation of nano-sized PEGylated Fe₃O₄@Ag particles, i.e., the main purpose was the synthesis of magnetic nanoparticles with a functionalized surface. Firstly, Fe₃O₄ particles were prepared via the Massart process. Next, Ag+ reduction was conducted in the presence of Fe₃O₄ particles to form a nanosilver coating. The reaction was performed with arabic gum as a stabilizing agent. Sound energy-using sonication was applied to disintegrate the particles’ agglomerates. Next, the PEGylation process aimed at the formation of a coating on the particles’ surface using PEG (poly(ethylene glycol)) has been performed. It was proved that the arabic gum limited the agglomeration of nanoparticles, which was probably caused by the steric effect caused by the branched compounds from the stabilizer that adsorbed on the surface of nanoparticles. This effect was also enhanced by the electrostatic repulsions. The process of sonication caused the disintegration of aggregates. Formation of iron (II, III) oxide with a cubic structure was proved by diffraction peaks. Formation of a nanosilver coating on the Fe₃O₄ nanoparticles was confirmed by diffraction peaks with 2θ values 38.15° and 44.35°. PEG coating on the particles’ surface was proven via FT-IR (Fourier Transform Infrared Spectroscopy) analysis. Obtained PEG–nanosilver-coated Fe₃O₄ nanoparticles may find applications as carriers for targeted drug delivery using an external magnetic field. Full article