Optimization of hematite nanoparticles from natural ore as novel imaging agents: A Green Chemistry approach.

In this research, we propose an environmentally friendly method for producing hematite nanoparticles (H-NPs) from natural hematite ore, focusing on their application as efficient contrast agents in x-ray and computed tomography (CT) imaging for medical purposes. The process involves the reduction of iron oxide within the ore to attain the desired hematite phase, crucial for synthesizing H-NPs. To ensure sustainability, we adopted a Green Chemistry approach, utilizing a combination of carbon soot and limestone for the purification process, thereby achieving eco-conscious production. The produced H-NPs were thoroughly characterized using various analytical techniques, such as x-ray fluorescence (XRF), x-ray diffraction (XRD), Fourier transmission infrared spectroscopy (FT-IR), and FESEM-EDX (field emission scanning electron microscopy-energy-dispersive x-ray spectroscopy). XRD analysis confirmed the crystalline rhombohedral hexagonal lattice structure, while FT-IR spectra indicated the presence of characteristic Fe-O stretching modes in line with the expected molecular composition. FESEM-EDX imaging unveiled agglomerated particles, ranging in size from 54.6 to 149.9 nm for iron ore and 22 nm for H-NPs. These particles were primarily composed of iron (Fe) and oxygen (O). The magnetic properties of the H-NPs were investigated through vibrating sample magnetometer (VSM) studies, highlighting their distinct ferromagnetic behavior. Of particular significance, the H-NPs demonstrated exceptional performance as contrast agents in both x-ray and CT imaging. Even at minimal concentrations, they exhibited remarkable x-ray absorption capabilities. CT scans further validated their exceptional absorptive capacity. These findings emphasize the potential of H-NPs as valuable assets in medical imaging, serving as sustainable tools for enhanced diagnostic applications. The study showcases an eco-conscious approach to harnessing natural resources, paving the way for a greener and more effective utilization of H-NPs in the medical imaging landscape.

Efficient adsorption of Cr (VI) onto hematite nanoparticles: ANN, ANFIS modelling, isotherm, kinetic, thermodynamic studies and mechanistic insights.

Hematite nanoparticles (AF-Fe2O3NPs) were prepared through a simple method utilizing Acacia falcata leaf extract in this investigation. The nanoparticles were extensively characterized to understand their specific properties. FESEM images revealed agglomerated surface morphology, while EDS confirmed the existence of elemental components, including Fe, O, and C. The mesoporous nature of AF-Fe2O3NPs with a pore diameter of 3.77 nm was determined through BET studies. XRD analysis indicated the crystallinity, with lattice parameters characteristic of hematite nanoparticles (a = 0.504 nm and c = 1.381 nm). Superparamagnetic property of the AF-Fe2O3NPs was affirmed from the saturation magnetization (2.98 emu/g) without any hysteresis. Subsequently, AF-Fe2O3NPs were used as adsorbent for the removal of Cr (VI) from aqueous solution. The experimental data were subjected to machine learning (ML) models, specifically ANN and ANFIS, to predict Cr (VI) removal. Both ML models exhibited excellent predictive capabilities, with high R2 values (>0.99) and low error indices such as MSE, RMSE, and MAE. Furthermore, comprehensive kinetic, isotherm, and thermodynamic studies were conducted to gain insights into the behavior and sorption mechanisms of Cr (VI). The Hill model, a statistical physics model, demonstrated an outstanding fit compared to conventional isotherms. It revealed a saturation adsorption potential of 12.91 mg/g at pH 2, 1.5 g/L dose, and a temperature of 30 °C, corroborating physisorption as the dominant mechanism. XPS results confirmed Cr (VI) reduction to Cr (III) through the appearance of specific peaks at 577.18 and 587.08 eV. Thermodynamic investigations established the endothermicity and spontaneity of the adsorption. In summary, the hematite nanoparticles synthesized in this study exhibit promising potential to remove Cr (VI) from aqueous streams, making them a viable option for water treatment applications.

Facet-Specific Photocatalytic Degradation of Extracellular Antibiotic Resistance Genes by Hematite Nanoparticles in Aquatic Environments.

The persistence of extracellular antibiotic resistance genes (ARGs) in aquatic environments has attracted increasing attention due to their potential threat to public health and the environment. However, the fate of extracellular ARGs in receiving water remains largely unknown. This study investigated the influence of hematite nanoparticles, a widespread natural mineral, on the photodegradation of extracellular ARGs in river water. Results showed that under exposure to visible light, hematite nanoparticles, at environmental concentrations, resulted in a 3-5 orders of magnitude reduction in extracellular ARGs. This photodegradation of extracellular ARGs is shown to be facet-dependent; the (001) facet of hematite demonstrates a higher removal rate than that of the (100) facet, which is ascribed to its enhanced adsorption capability and higher hydroxyl radical (•OH) production. Density functional theory (DFT) calculations corroborate this finding, indicating elevated iron density, larger adsorption energy, and lower energy barrier of •OH formation on the (001) facet, providing more active sites and •OH generation for extracellular ARG interaction. Gel electrophoresis and atomic force microscopy analyses further confirm that the (001) facet causes more substantial damage to extracellular ARGs than the (100) facet. These findings pave the way for predicting the photodegradation efficiency of hematite nanoparticles with varied facets, thereby shedding light on the inherent self-purification capacity for extracellular ARGs in both natural and engineered aquatic environments.

Hematites Precipitated in Alkaline Precursors: Comparison of Structural and Textural Properties for Methane Oxidation.

Hematite (α-Fe2O3) catalysts prepared using the precipitation methods was found to be highly effective, and therefore, it was studied with methane (CH4), showing an excellent stable performance below 500 °C. This study investigates hematite nanoparticles (NPs) obtained by precipitation in water from the precursor of ferric chloride hexahydrate using precipitating agents NaOH or NH4OH at maintained pH 11 and calcined up to 500 °C for the catalytic oxidation of low concentrations of CH4 (5% by volume in air) at 500 °C to compare their structural state in a CH4 reducing environment. The conversion (%) of CH4 values decreasing with time was discussed according to the course of different transformation of goethite and hydrohematites NPs precursors to magnetite and the structural state of the calcined hydrohematites. The phase composition, the size and morphology of nanocrystallites, thermal transformation of precipitates and the specific surface area of the NPs were characterized in detail by X-ray powder diffraction, transmission electron microscopy, infrared spectroscopy, thermal TG/DTA analysis and nitrogen physisorption measurements. The results support the finding that after goethite dehydration, transformation to hydrohematite due to structurally incorporated water and vacancies is different from hydrohematite α-Fe2O3. The surface area SBET of Fe2O3_NH-70 precipitate composed of protohematite was larger by about 53 m2/g in comparison with Fe2O3_Na-70 precipitate composed of goethite. The oxidation of methane was positively influenced by the hydrohematites of the smaller particle size and the largest lattice volume containing structurally incorporated water and vacancies.

Synthesis, characterization and anticancer activity of the green-synthesized hematite nanoparticles.

The conventional synthesis of hematite nanoparticles (HNPs) is expensive and creates secondary contaminants. Therefore, to combat these issues, there is a requirement for a cheap, effective, and eco-friendly technique. Herein, HNPs were prepared using the fruit extract of Spondias pinnata - an abundant source available in Western-coastal India. The polyphenolic compounds aided the synthesis process and the entire procedure was very rapid. The obtained HNPs had needle-like morphology with agglomerations due to the magnetic interactions as seen in FESEM and HRTEM images. Fe and O elements were noticed in EDS results. The crystalline nature and crystal phase were confirmed from XRD and SAED patterns. The lattice parameters of HNPs were in tandem with the literature. Fe-O crystalline vibrations were noticed in FTIR studies. VSM results portrayed the superparamagnetic nature of HNPs with a high magnetic saturation value of 8.949 emu/g and a negligible hysteresis loop. Thermal stability was ascertained using TGA results with 32% overall weight loss. XPS studies revealed the existence of pure HNPs with signature peaks. Raman spectrum showed the bands specific for HNPs, comparable to the commercial one. In addition, the HNPs were mesoporous with a high surface area (72.04 m2/g) - higher than the commercial one. The anticancer potential of the HNPs was successfully demonstrated against two mammalian cancer cell lines. Therefore, the HNPs synthesized in this study could be applied in various biomedical fields, especially for anticancer formulations.

Synthesis and characterization ofα-Fe2O3nanoparticles showing potential applications for sensing quaternary ammonium vapor at room temperature.

P-type and n-type metal oxide semiconductors are widely used in the manufacture of gas sensing materials, due to their excellent electronic, electrical and electrocatalytic properties. Hematite (α-Fe2O3) compound has been reported as a promising material for sensing broad types of gases, due to its affordability, good stability and semiconducting properties. In the present work, the efficient and easy-to-implement sol-gel method has been used to synthesizeα-Fe2O3nanoparticles (NPs). The TGA-DSC characterizations of the precursor gel provided information about the phase transformation temperature and the mass percentage of the hematite NPs. X-ray diffraction, transmission electron microscopy and x-ray photoelectron spectroscopy data analyses indicated the formation of two iron oxide phases (hematite and magnetite) when the NPs are subjected to thermal treatment at 400 °C. Meanwhile, only the hematite phase was determined for thermal annealing above 500 °C up to 800 °C. Besides, the crystallite size shows an increasing trend with the thermal annealing and no defined morphology. A clear reduction of surface defects, associated with oxygen vacancies was also evidenced when the annealing temperature was increased, resulting in changes on the electrical properties of hematite NPs. Resistive gas-sensing tests were carried out using hematite NPs + glycerin paste, to detect quaternary ammonium compounds. Room-temperature high sensitivity values (Sr âˆ¼ 4) have been obtained during the detection of ∼1 mM quaternary ammonium compounds vapor. The dependence of the sensitivity on the particle size, the mass ratio of NPs with respect to the organic ligand, changes in the dielectric properties, and the electrical conduction mechanism of gas sensing was discussed.

Mono-Doped and Co-Doped Nanostructured Hematite for Improved Photoelectrochemical Water Splitting.

In this study, zinc-doped (α-Fe2O3:Zn), silver-doped (α-Fe2O3:Ag) and zinc/silver co-doped hematite (α-Fe2O3:Zn/Ag) nanostructures were synthesized by spray pyrolysis. The synthesized nanostructures were used as photoanodes in the photoelectrochemical (PEC) cell for water-splitting. A significant improvement in photocurrent density of 0.470 mAcm-2 at 1.23 V vs. reversible hydrogen electrode (RHE) was recorded for α-Fe2O3:Zn/Ag. The α-Fe2O3:Ag, α-Fe2O3:Zn and pristine hematite samples produced photocurrent densities of 0.270, 0.160, and 0.033 mAcm-2, respectively. Mott-Schottky analysis showed that α-Fe2O3:Zn/Ag had the highest free carrier density of 8.75 × 1020 cm-3, while pristine α-Fe2O3, α-Fe2O3:Zn, α-Fe2O3:Ag had carrier densities of 1.57 × 1019, 5.63 × 1020, and 6.91 × 1020 cm-3, respectively. Electrochemical impedance spectra revealed a low impedance for α-Fe2O3:Zn/Ag. X-ray diffraction confirmed the rhombohedral corundum structure of hematite. Scanning electron microscopy micrographs, on the other hand, showed uniformly distributed grains with an average size of <30 nm. The films were absorbing in the visible region with an absorption onset ranging from 652 to 590 nm, corresponding to a bandgap range of 1.9 to 2.1 eV. Global analysis of ultrafast transient absorption spectroscopy data revealed four decay lifetimes, with a reduction in the electron-hole recombination rate of the doped samples on a timescale of tens of picoseconds.

Superparamagnetic hematite spheroids synthesis, characterization, and catalytic activity.

The leaf extract of Muntingia calabura is being first reported to be used for the synthesis superparamagnetic hematite nanoparticles by following the green-chemistry approach. Field Emission - Scanning Electron Microscopic image revealed the formation of irregular nano spheroids averaging at 48.57 nm in size and characteristic of Fe and O atoms, as revealed by Energy Dispersive X-Ray spectrum. X-ray diffraction analysis results proved the crystallinity of hematite diffraction planes with crystallite sizes averaging at 30.68 nm. The lattice parameter values stayed concordant with the literature. The superparamagnetic nature was attested by the high value of saturation magnetism (2.20 emu/g) with negligible coercivity and retentivity. Fourier Transform Infrared Spectroscopy results affirmed numerous moieties involved in the synthesis of hematite nanoparticles and the existence of signature Fe-O bands. Thermogravimetric analysis studies portrayed the thermal behavior nanoparticles with 28% weight loss and thermal stability was attained after 700 °C. X-ray photoelectron spectroscopy analysis confirmed the valence states of Fe and O in the hematite nanoparticles and ascertained the purity. The mesoscopic structure was revealed by Brunauer-Emmett-Teller studies with considerable surface area (112.50 m2/g). The Fenton-like catalysis mediated by the nanoparticle sample was demonstrated by degrading methylene blue dye. The remarkable degradation efficiency of 93.44% was obtained and the kinetics was conformed to a second-order model with a high R2 value. Therefore, the highly crystalline and mesoporous superparamagnetic hematite spheroids prepared using the leaf extract of M. calabura would find promising applications in various catalysis processes.

Synthesis and characterization of polyphenols functionalized graphitic hematite nanocomposite adsorbent from an agro waste and its application for removal of Cs from aqueous solution.

In this study, Polyphenols functionalized Graphitic Hematite Nanocomposite (PGHN) was used as an adsorbent to remove Caesium (Cs) ions from a simulated solution. The nanocomposite was produced by synthesizing iron oxide nanoparticles using orange peel extract (OPE) as the reducing and capping agent in the presence of graphite produced from sugarcane bagasse. The nanocomposite exhibited a scaly morphology and the mean particle size of rhombohedral structured hematite nanoparticles was found to be 148.9 nm. The simulated solution of Cs ions was treated with PGHN and the treatment conditions were optimized by batch method. The concentration of Cs ion in the treated solution was determined using atomic emission spectroscopy (AES). The maximum Cs adsorption of 97.95% was attained at an optimum condition of pH - 9.0 and adsorbent dose - 70 mg/mL for treatment period of 110 min. The experimental data of adsorption fitted well with pseudo 1st order kinetics and was favorable for both Langmuir and Freundlich isotherm models. The study reports a facile method for the production of nanocomposite using agro-wastes such as sugarcane bagasse and orange peels. The synthesized nanocomposite was used as an adsorbent for the removal of toxic Cs and can be further used for industrial wastewater treatment.

Uptake of hematite nanoparticles in maize and their role in cell cycle dynamics, PCNA expression and mitigation of cadmium stress.

Cadmium toxicity is considered a major threat to several crops worldwide. Hematite nanoparticles (NPs), due to their small size and large specific surface area, could be applied as an adsorbent for toxic heavy metals in soil. Also, they serve as an efficient nano-fertilizer, promoting Fe availability and biomass production in plants, thus enabling Cd2+ -induced stress tolerance. The phytotoxicity of five different concentrations of hematite NPs, ranging from 500 to 8,000 mg·kg-1 , and Cd2+ concentrations (110 or 130 mg·kg-1 Cd2+ ) alone or combined with 500 mg·kg-1 NPs was evaluated in maize. The changes in fresh weight, element analysis, cell cycle regulation, DNA banding patterns and proliferating cell nuclear antigen (PCNA) expression were used as biomarkers. The results revealed that increased fresh weight and fewest polymorphic DNA bands were detectable after treatment with 500 mg·kg-1 NPs. However, at 8,000 mg·kg-1 NPs, PCNA expression increased significantly, which resulted in cell cycle arrest at the G1/S checkpoint in roots. Significant reductions in fresh weight, altered nutrient profiles and cell cycle perturbations are considered symptoms of Cd2+ toxicity in maize. Conversely, amending 500 mg·kg-1 NPs with 130 mg·kg-1 Cd2+ increased fresh weight, Fe concentration and genomic template stability, while reducing Cd2+ uptake and PCNA1 expression. Overall, 8,000 mg·kg-1 hematite NPs interfered with the cellular homeostatic balance of maize, resulting in a cascade of genotoxic events, leading to growth inhibition. Although 500 mg·kg-1 hematite NPs alleviated Cd2+ -induced DNA damage to a certain extent, their impact on cell cycle progression requires further verification.

Bacteria compete with hematite nanoparticles during their uptake by the ciliate Tetrahymena thermophila.

Bacterial accumulation of engineered nanoparticles (NPs) result in their transfer along the food chain. However, there are a lot of NPs not associated with bacteria. Whether bacteria, as representative biotic particles, influence the biological uptake of these non-associated NPs in aquatic ecosystems is unclear. In the present study, we examined the effects of four bacterial species on the uptake kinetics of polyacrylate-coated hematite nanoparticles (HemNPs) by the ciliate Tetrahymena thermophila. The HemNPs were well dispersed. Their adsorption on the bacteria was low with negligible uptake by T. thermophila through bacterial ingestion. This result demonstrated the feasibility of examining the effects of bacteria on the uptake of non-associated HemNPs. Our study further showed that all four bacterial species inhibited the uptake of HemNPs by T. thermophila; however, the effects of the bacterial cells on the physiological activities of the ciliate with respect to its uptake of HemNPs were negligible. In the absence of phagocytosis by T. thermophila, none of the bacteria inhibited HemNP uptake. This observation suggested that bacterial cells competed with the HemNPs for uptake via phagocytosis. Therefore, in evaluations of the environmental risks of NPs, their competition with biotic particles should be taken into account.

New Sustainable, Scalable and One-Step Synthesis of Iron Oxide Nanoparticles by Ion Exchange Process.

This work introduces an innovative, sustainable, and scalable synthesis of iron oxides nanoparticles (NPs) in aqueous suspension. The method, based on ion exchange process, consists of a one-step procedure, time and energy saving, operating in water and at room temperature, by cheap and renewable reagents. The influence of both oxidation state of the initial reagent and reaction atmosphere is considered. Three kinds of iron nanostructured compounds are obtained (2-lines ferrihydrite; layered-structure iron oxyhydroxide δ-FeOOH; and cubic magnetite), in turn used as precursors to obtain hematite and maghemite NPs. All the produced NPs are characterized by a high purity, small particles dimensions (from 2 to 50 nm), and high specific surface area values up to 420 m2/g, with yields of production >90%. In particular, among the most common iron oxide NPs, we obtained cubic magnetite NPs at room temperature, characterized by particle dimensions of about 6 nm and a surface area of 170 m2/g. We also obtained hematite NPs at very low temperature conditions (that is 2 h at 200 °C), characterized by particles dimensions of about 5 nm with a surface area value of 200 m2/g. The obtained results underline the strength of the synthetic method to provide a new, sustainable, tunable, and scalable high-quality production.

Effect of Morphologically Controlled Hematite Nanoparticles on the Properties of Fly Ash Blended Cement.

Several types of hematite nanoparticles (α-Fe2O3) have been investigated for their effects on the structure and properties of fly ash (FA) blended cement. All synthesized nanoparticles were found to be of spherical shape, but of different particle sizes ranging from 10 to 195 nm depending on the surfactant used in their preparation. The cement hydration with time showed 1.0% α-Fe2O3 nanoparticles are effective accelerators for FA blended cement. Moreover, adding α-Fe2O3 nanoparticles in FA blended cement enhanced the compressive strength and workability of cement. Nanoparticle size and size distribution were important for optimal filling of various size of pores within the cement structure.

Toxicological evaluation of biosynthesised hematite nanoparticles in vivo.

In recent years, nanomaterials have been widely used in consumer products. High reactivity of metallic nanoparticles and its bioaccumulation in biological systems are the main causes of concern over their safety to human health and environment. The available information related to the safety of several nanomaterials is insufficient. Hematite nanoparticles are proposed for various applications. Ecotoxicological studies of hematite nanoparticles are very limited. In the present study, biosynthesised hematite nanoparticles using Bacillus cereus were evaluated for its acute oral toxicity in mice following OECD guidelines. A dose of 2 g/kg/p.o was administered to Swiss albino mice through gastric oral feeding tube and observed for 14 days. After two weeks blood samples were collected and subjected for evaluation of haematological parameters and biochemical analysis. There was no mortality and toxic signs of animals till the end of observational period. The animals were sacrificed and organs like liver and kidneys were isolated to study the histopathological changes. The results of the study revealed that there was no drastic change in parameters except slight change in bilirubin in the hematite nanoparticle treated mice. Biosynthesised hematite nanoparticles were assayed for toxicity in Artemia salina. Cysts treated with higher concentrations of hematite nanoparticles showed small sized nauplii. Biosynthesised hematite nanoparticles were found to be non-toxic to A. salina nauplii in lower concentrations.

Uptake, translocation, and physiological effects of hematite (α-Fe2O3) nanoparticles in barley (Hordeum vulgare L.).

There has been a growing concern with the environmental influences of nanomaterials due to recent developments in nanotechnology. This study investigates the impact and fate of hematite nanoparticles (α-Fe2O3 NPs) (∼14 nm in size) on a crop species, barley (Hordeum vulgare L.). For this purpose, hematite NPs (50, 100, 200, and 400 mg/L) were hydroponically applied to barley at germination and seedling stages (three weeks). Inductively coupled plasma mass spectrophotometry (ICP-MS) along with vibrating sample magnetometer (VSM) techniques were used to track the NPs in plant tissues. The effects of NPs on the root cells were observed by scanning electron microscopy (SEM) and confocal microscopy. Results revealed that α-Fe2O3 NPs significantly reduced the germination rate (from 80% in control to 30% in 400 mg/L), as well as chlorophyll (36-39%) and carotenoid (37%) contents. Moreover, the treatment led to a significant decline in the quantum yield of photosystem II (Fv/Fm). Leaf VSM analysis indicated a change in magnetic signal for NPs-treated samples compared with untreated ones, which is mostly attributed to the iron (Fe) ions incorporated within the leaf tissue. Besides, Fe content in the roots and leaf had gradually increased by the increasing doses of NPs, which was confirming NPs' translocation to the aerial parts. Microscopic observations revealed that α-Fe2O3 NPs altered root cell morphology and led to the injury of cell membranes. This study, in the light of our findings, shows that α-Fe2O3 NPs (∼14 nm in size) are taken up by the roots of the barley plants, and migrate to the plant leaves. Besides, NPs are phytotoxic for barley as they inhibit germination and pigment biosynthesis. This inhibition is probably due to the injury of the cell membranes in the roots. Therefore, the use of hematite NPs in agriculture and thereby their environmental diffusion must be addressed carefully.

A low-cost solvent-free method to synthesize α-Fe2O3 nanoparticles with applications to degrade methyl orange in photo-fenton system.

Hematite nanoparticles (α-Fe2O3 NPs) were successfully synthesized by a low-cost solvent-free reaction using Ferrous sulfate waste (FeSO4·7H2O) and pyrite (FeS2) as raw materials and employed for the decolorization of Methyl Orange by the photo-Fenton system. The properties of α-Fe2O3 NPs before and after photo-Fenton reaction were characterized by X-ray powder diffraction (XRD), Field emission scanning electron microscopy (FESEM), Fourier transform infrared (FT-IR) spectrum and X-ray photoelectron spectroscopy (XPS), and the optical properties of α-Fe2O3 NPs were analyzed by UV-vis diffuse reflectance spectra (UV-vis DRS) and Photoluminescence (PL) spectra. The analytic results showed that the as-formed samples having an average diameter of ~50 nm exhibit pure phase hematite with sphere structure. Besides, little differences were found by comparing the characterization data of the particles before and after the photo-Fenton reaction, indicating that the photo-Fenton reaction was carried out in solution rather than on the surface of α-Fe2O3 NPs. A 24 central composite design (CCD) coupled with response surface methodology (RSM) was applied to evaluate and optimize the important variables. A significant quadratic model (P-value<0.0001, R2 = 0.9664) was derived using an analysis of variance (ANOVA), which was adequate to perform the process variables optimization. The optimal process conditions were performed to be 395 nm of the light wavelength, pH 3.0, 5 mmol/L H2O2 and 1 g/L α-Fe2O3, and the decolorization efficiency of methyl orange was 99.55% at 4 min.

Hematite Nanoparticles from Unexpected Reaction of Ferrihydrite with Concentrated Acids for Biomedical Applications.

The development of synthetic ways to fabricate nanosized materials with a well-defined shape, narrow-sized distribution, and high stability is of great importance to a rapidly developing area of nanotechnology. Here, we report an unusual reaction between amorphous two-line ferrihydrite and concentrated sulfuric or other mineral and organic acids. Instead of the expected dissolution, we observed the formation of new narrow-distributed brick-red nanoparticles (NPs) of hematite. Different acids produce similar nanoparticles according to scanning (SEM) and transmission electron microscopy (TEM), selected area electron diffraction (SAED), X-ray diffraction (XRD), infrared spectroscopy (FTIR), and energy-dispersive X-ray spectroscopy (EDX). The reaction demonstrates new possibilities for the synthesis of acid-resistant iron oxide nanoparticles and shows a novel pathway for the reaction of iron hydroxide with concentrated acids. The biomedical potential of the fabricated nanoparticles is demonstrated by the functionalization of the particles with polymers, fluorescent labels, and antibodies. Three different applications are demonstrated: i) specific targeting of the red blood cells, e.g., for red blood cell (RBC)-hitchhiking; ii) cancer cell targeting in vitro; iii) infrared ex vivo bioimaging. This novel synthesis route may be useful for the development of iron oxide materials for such specificity-demanding applications such as nanosensors, imaging, and therapy.

Nano-Sized Fe(III) Oxide Particles Starting from an Innovative and Eco-Friendly Synthesis Method.

This paper introduces an original, eco-friendly and scalable method to synthesize ferrihydrite nanoparticles in aqueous suspensions, which can also be used as a precursor to produce α-hematite nanoparticles. The method, never used before to synthesize iron oxides, is based on an ion exchange process allowing to operate in one-step, with reduced times, at room temperature and ambient pressure, and using cheap or renewable reagents. The influence of reagent concentrations and time of the process on the ferrihydrite features is considered. The transformation to hematite is then analyzed and discussed in relation to different procedures: (1) A natural aging in the water at room temperature; and (2) heat treatments at different temperatures and times. Structural and morphological features of the obtained nanoparticles are investigated by means of several techniques, such as X-ray diffraction, X-ray photoelectron spectroscopy, attenuated total reflectance Fourier transform infrared spectroscopy, transmission and scanning electron microscopy, thermal analysis, nitrogen adsorption and magnetic measurements. Ferrihydrite shows the typical spherical morphology and a very high specific surface area of 420 m2/g. Rhombohedral or plate-like hexagonal hematite nanoparticles are obtained by the two procedures, characterized by dimensions of 50 nm and 30 nm, respectively, and a specific surface area up to 57 m2/g, which is among the highest values reported in the literature for hematite NPs.

Waterborne and dietary accumulation of well-dispersible hematite nanoparticles by zebrafish at different life stages.

The widespread use of nanoparticles (NPs) has drawn considerable attention because of their potential toxicity and the environmental consequences thereof. However, the effects of the exposure route and life stage of an organism on the bioaccumulation and toxicity of NPs are largely unknown. In the present study, we investigated the accumulation kinetics (uptake, assimilation, and efflux) and tissue distribution of waterborne and dietary hematite NPs (HemNPs) during three life stages (embryo, larva, and adult) of the zebrafish Danio rerio. For all zebrafish life stages, the waterborne accumulation of well-dispersed HemNPs increased linearly with exposure time but decreased after reaching a maximum. The increase in HemNPs accumulation followed the order embryo > larva > adult. Compared with the waterborne route, the dietary accumulation of HemNPs in larval and adult zebrafish fluctuated, reaching a maximum after each food refreshment and then decreasing until the next food addition. Similar to waterborne exposure, adult fish accumulated less dietary HemNPs than did larvae. Nevertheless, dietary HemNPs mostly accumulated in the intestinal tract, with smaller amounts in the truncus, head, and gills, as compared with their waterborne counterparts. Moreover, in the gonad no dietary HemNPs were detected whereas accumulation via waterborne HemNPs was significant. Despite the low assimilation efficiency of dietary HemNPs, biodynamic modeling showed that the diet was the main source of particle accumulation in zebrafish. Thus, both the life stage and the exposure route should be considered in evaluations of the environmental risks of NPs.

Efficient photocatalytic degradation of malachite green dye using facilely synthesized hematite nanoparticles from Egyptian insecticide cans.

In the present study, a combustion method was applied for the production of hematite nanoparticles from Egyptian iron waste using l-arginine (The sample was named HA) and glutamine (The sample was named HG) as organic fuels, respectively. XRD confirmed that the HA and HG products have crystallite sizes of 48 and 56 nm, respectively. Also, HR-TEM demonstrated that spherical and irregular shapes have an average diameter of 45 and 59  nm were observed in the HA and HG samples, respectively. Besides, FE-SEM elucidated that spherical and irregular shapes have an average size of 142 and 196 nm were observed in the HA and HG samples, respectively. In addition, FT-IR confirmed that the peaks which were detected at 518 and 430 cm-1 are because of vibrations of Fe-O bond. Moreover, the value of the energy gap for the HA and HG samples was 1.00 and 1.45 eV, respectively. Furthermore, the PL emission spectra elucidated that the emission intensity of the HA sample was less than that of the HG sample. So, e-/h+ recombination rate of the HA sample was less than that of the HG sample. Hence, the photocatalytic degradation of malachite green dye using the HA sample was larger than that using the HG sample. In the absence of H2O2, the % degradation of malachite green dye under the influence of UV using HA and HG samples was 46.29 and 39.72 % after 3 h, respectively. Also, in the presence of H2O2, the % degradation of malachite green dye under the influence of UV using HA and HG samples was 100 % after 60 and 70 min, respectively.