Synthetic Iron Research Articles

Repurposing spent filter sand from iron and manganese removal systems as an adsorbent for treating arsenic contaminated drinking water

Waterworks which utilise river bank filtration water sources often have to apply aeration and sand filtration to remove iron and manganese during the drinking water treatment process. After some time, the sand becomes saturated and the spent filter sand (SFS) must be disposed of and replaced. In order to valorize this waste stream, this paper investigates the reuse of SFS as an adsorbent for the treatment of arsenic contaminated drinking water. The arsenic removal performance of SFS is compared with two synthetic iron oxide coated sands (IOCS). The sorbents were first characterized by SEM, EDS, BET specific surface area, and point of zero charge (pHpzc) measurements, and then investigated under a variety of conditions. The surface of the SFS was revealed to be coated with iron manganese binary oxide. The Freundlich model best described the isotherm experiment data, indicating a non monolayer adsorption model for arsenic adsorption on the three IOCS investigated. As(III) and As(V) removals were negatively effected by the presence of PO43− and HA anions as they competed with the arsenic species for adsorption sites. However, given the status of SFS as a waste material, the results obtained in this paper suggest it may be successfully reused as a very economically and environmentally sustainable solution for small waterworks requiring both As(V) and As(III) removal during drinking water treatment.

Adsorption of Strontium onto Synthetic Iron(III) Oxide up to High Ionic Strength Systems

In this work, the adsorption behavior of Sr onto a synthetic iron(III) oxide (hematite with traces of goethite) has been studied. This solid, which might be considered a representative of Fe3+ solid phases (iron corrosion products), was characterized by X-Ray Diffraction (XRD) and X-Ray Photoelectron Spectroscopy (XPS), and its specific surface area was determined. Both XRD and XPS data are consistent with a mixed solid containing more than 90% hematite and 10% goethite. The solid was further characterized by fast acid-base titrations at different NaCl concentrations (from 0.1 to 5 M). Subsequently, for each background NaCl concentration used for the acid-base titrations, Sr-uptake experiments were carried out involving two different levels of Sr concentration (1 × 10−5 and 5 × 10−5 M, respectively) at constant solid concentration (7.3 g/L) as a function of −log([H+]/M). A Surface Complexation Model (SCM) was fitted to the experimental data, following a coupled Pitzer/surface complexation approach. The Pitzer model was applied to aqueous species. A Basic Stern Model was used for interfacial electrostatics of the system, which includes ion-specific effects via ion-specific pair-formation constants, whereas the Pitzer-approach involves ion-interaction parameters that enter the model through activity coefficients for aqueous species. A simple 1-pK model was applied (generic surface species, denoted as >XOH−1/2). Parameter fitting was carried out using the general parameter estimation software UCODE, coupled to a modified version of FITEQL2. The combined approach describes the full set of data reasonably well and involves two Sr-surface complexes, one of them including chloride. Monodentate and bidentate models were tested and were found to perform equally well. The SCM is particularly able to account for the incomplete uptake of Sr at higher salt levels, supporting the idea that adsorption models conventionally used in salt concentrations below 1 M are applicable to high salt concentrations if the correct activity corrections for the aqueous species are applied. This generates a self-consistent model framework involving a practical approach for semi-mechanistic SCMs. The model framework of coupling conventional electrostatic double layer models for the surface with a Pitzer approach for the bulk solution earlier tested with strongly adsorbing solutes is here shown to be successful for more weakly adsorbing solutes.

Synthesis and Characterization of Nano Fe and Mn (hydr)oxides to Be Used as Natural Sorbents and Micronutrient Fertilizers

Fe and Mn (hydr)oxides are widely used as contaminant sorbents in water/wastewater systems but their potential use as micronutrient fertilizers is still poorly known. In this research, four nano-metal (hydr)oxides (amorphous Mn oxide (AMO), Fe-Mn binary oxide (FMBO), two-line ferrihydrite (2L-Fh) and goethite) were successfully synthesized and completely characterized (infrared and Mössbauer spectroscopy, X-ray diffraction particle size, specific surface area, point of zero charge). AMO, FMBO and 2L-Fh were introduced to interact with AgNO3 (20.0 µM) and TlNO3 (100.0 µM) diluted solutions for three days to check their potential capability as potential Ag+ and Tl+ adsorbents. AMO and FMBO (4% w/w) were tested as nanofertilizers by arranging a hydroponic bioassay for 35 days on white lupin culture as a Mn-hyperaccumulator plant model. AMO structure was identified as an amorphous mixture of Mn oxides while FMBO was an Fe dopped birnessite. Both materials were efficient in extracting Ag+ and Tl+ although large Mn concentration was released from FMBO to the solutions. AMO and FMBO promoted Fe and Mn nutrition in plants. Synthetic iron chelate (Fe-EDDHA), present in the nutrient dissolution, could be adsorbed onto AMO surface by producing Fe and Mn accumulation in roots and increasing Mn uptake rate without toxicity symptoms. Therefore, AMO and FMBO not only demonstrated their efficiency as adsorbents, but also displayed they would be promising nanomaterials as micronutrient fertilizers.

C-H Bond Cleavage by Bioinspired Nonheme Metal Complexes.

The functionalization of C-H bonds is one of the most challenging transformations in synthetic chemistry. In biology, these processes are well-known and are achieved with a variety of metalloenzymes, many of which contain a single metal center within their active sites. The most well studied are those with Fe centers, and the emerging experimental data show that high-valent iron oxido species are the intermediates responsible for cleaving the C-H bond. This Forum Article describes the state of this field with an emphasis on nonheme Fe enzymes and current experimental results that provide insights into the properties that make these species capable of C-H bond cleavage. These parameters are also briefly considered in regard to manganese oxido complexes and Cu-containing metalloenzymes. Synthetic iron oxido complexes are discussed to highlight their utility as spectroscopic and mechanistic probes and reagents for C-H bond functionalization. Avenues for future research are also examined.

Magnetic Properties of Bacterial Magnetosomes Produced by Magnetospirillum caucaseum SO-1.

In this study, the magnetic properties of magnetosomes isolated from lyophilized magnetotactic bacteria Magnetospirillum caucaseum SO-1 were assessed for the first time. The shape and size of magnetosomes and cell fragments were studied by electron microscopy and dynamic light scattering techniques. Phase and elemental composition were analyzed by X-ray and electron diffraction and Raman spectroscopy. Magnetic properties were studied using vibrating sample magnetometry and electron paramagnetic resonance spectroscopy. Theoretical analysis of the magnetic properties was carried out using the model of clusters of magnetostatically interacting two-phase particles and a modified method of moments for a system of dipole–dipole-interacting uniaxial particles. Magnetic properties were controlled mostly by random aggregates of magnetosomes, with a minor contribution from preserved magnetosome chains. Results confirmed the high chemical stability and homogeneity of bacterial magnetosomes in comparison to synthetic iron oxide magnetic nanoparticles.

Biomimetic Iron Complex Achieves TET Enzyme Reactivity**

AbstractThe epigenetic marker 5‐methyl‐2′‐deoxycytidine (5mdC) is the most prevalent modification to DNA. It is removed inter alia via an active demethylation pathway: oxidation by Ten‐Eleven Translocation 5‐methyl cytosine dioxygenase (TET) and subsequent removal via base excision repair or direct demodification. Recently, we have shown that the synthetic iron(IV)‐oxo complex [FeIV(O)(Py5Me2H)]2+ (1) can serve as a biomimetic model for TET by oxidizing the nucleobase 5‐methyl cytosine (5mC) to its natural metabolites. In this work, we demonstrate that nucleosides and even short oligonucleotide strands can also serve as substrates, using a range of HPLC and MS techniques. We found that the 5‐position of 5mC is oxidized preferably by 1, with side reactions occurring only at the strand ends of the used oligonucleotides. A detailed study of the reactivity of 1 towards nucleosides confirms our results; that oxidation of the anomeric center (1′) is the most common side reaction.

Biomimetic Iron Complex Achieves TET Enzyme Reactivity*.

The epigenetic marker 5‐methyl‐2′‐deoxycytidine (5mdC) is the most prevalent modification to DNA. It is removed inter alia via an active demethylation pathway: oxidation by Ten‐Eleven Translocation 5‐methyl cytosine dioxygenase (TET) and subsequent removal via base excision repair or direct demodification. Recently, we have shown that the synthetic iron(IV)‐oxo complex [FeIV(O)(Py5Me2H)]2+ (1) can serve as a biomimetic model for TET by oxidizing the nucleobase 5‐methyl cytosine (5mC) to its natural metabolites. In this work, we demonstrate that nucleosides and even short oligonucleotide strands can also serve as substrates, using a range of HPLC and MS techniques. We found that the 5‐position of 5mC is oxidized preferably by 1, with side reactions occurring only at the strand ends of the used oligonucleotides. A detailed study of the reactivity of 1 towards nucleosides confirms our results; that oxidation of the anomeric center (1′) is the most common side reaction.

Novel synthetic iron (III) oxide-based force sensor

Recent progress observed in 'powdered composites', considered as advanced electrical inductance materials, brought some promising applications in flexible tactile, pressure and force sensors, which can be based on compressed metal oxide powder mass materials. Therefore, in this paper the evaluation of the resistance of force-sensitive material – synthetic iron (III) oxide powder – by implementing this material into the design of two force sensors is described. Two types of sensors with different external (height, diameter, construction) parameters were investigated. Sensor responses were evaluated by performing tests in static, long-term load and cyclic modes. Experimental results of loading cycle measurements revealed the hysteresis and nonlinearity of the sensors. Obtained sensors sensitivity, hysteresis, response time, and deformation dependencies on the applied compressive force promises a practical possibility to use the synthetic iron (III) oxide powder composite as sensitive material for force and pressure sensors. Developed sensors have simple construction, very high mechanical resistance, are very resistant to wear and environmental impact and can operate at high temperatures. The results of experimental research have defined the area of the possible implementation of the sensors based on iron (III) oxide powders. The active substance in the form of a powder is especially relevant in mechanical systems and robotics. Size and shape of powders can be easily adjusted to the working area parameters, the operating temperature range (can be up to 600 °C), and other industrial needs.

Sorption of arsenate(Ⅴ) to naturally occurring secondary iron minerals formed at different conditions: The relationship between sorption behavior and surface structure

Arsenic (As) is a problematic pollutant that can cause cancer and other chronic diseases due to its potential toxicity. Iron (oxyhydr)oxides can readily sorb As and play important roles in the geochemical cycle of As. Attention has mainly been given to the affinity and mechanism of As sorption by synthetic pure iron (oxyhydr)oxides, and little is known about the relationship between As behavior and multicomponent secondary iron minerals (SIMs) naturally formed in acid mine drainage (AMD). To investigate this relationship, we performed sorption kinetics, isotherm and competitive sorption experiments to investigate As(V) sorption behaviors on naturally formed SIMs harvested from different runoff zones of an abandoned coal mine. Several spectroscopic analyses were used to evaluate the structural and component changes and phase transformation. Three environmental SIMs formed at nascent (n-SIM), transient (t-SIM) and mature (m-SIM) stages were determined to be similar in the element components of Fe, S and O but different in structure. As(V) sorption behaviors on these environmental SIMs followed a pseudo-second-order kinetic model, and the sorption extent followed the sequence of n-SIM > t-SIM > m-SIM. As(V) sorption is not significantly influenced by Na+/Ca2+ concentration or ionic strength except for that of PO43−, and it slightly decreases as the Cr(Ⅲ) concentration increases but increases with increasing Sb(Ⅲ)/(V) concentration. The results of spectral analyses indicate that As(V) immobilization mainly depends on exchange with SO42− and surface complexation, along with the phase transformation of schwertmannite/jarosite to goethite and other phases. These findings are helpful for better understanding the geochemical behaviors of As(V) associated with environmental SIMs.

Recycling of iron-rich sediment for surface modification of filters for underground water deironing

Groundwater is one of the cleanest natural sources of drinking water available, which, at the same time, often requires deironing – removal of the dissolved iron ions – before the water could be used. In this paper, there are describe the preparation, characterization, and deironing properties of surface-modified refractory chamotte granules, used as active components of fillers for deironing filters. For this research, chamotte surface modification was made by solution combustion synthesis (SCS) approach of an aqueous solution of synthetic iron nitrate and citric acid with the different iron-to-chamotte ratios. An iron-rich precipitate from deironing filters was used as a source of iron for the preparation of a precursor solution. Obtained materials were characterized using diffraction, spectroscopic and microscopic methods. The SCS modification resulted in the formation of layers of hematite Fe3O4 nanocrystallites of ~5–15 nm on the surface of refractory chamotte granules. It was shown the effect of the dose of iron nitrate on the absorbed iron oxide species content on the surface of the modified chamotte granules and its influence on the surface and operational characteristics. Pilot-plant deironing tests showed that an increase in the concentration of iron on the chamotte granules surface from 5.8 wt% for unmodified samples, to 19.0, 48.7, and 55.8 wt% for the modified ones, led to the respective increase in the deironing efficiency from 41% to 65%, 73% and 78%, respectively.

Iron oxide pigments

Abstract Natural and synthetic iron oxide pigments are by far the most important colored pigments. Their high importance is based on the variety of stable colors ranging from yellow via orange, red and brown to black. Iron oxide yellow (α-FeOOH), iron oxide red (α-Fe2O3) and iron oxide black (Fe3O4) are the most important representatives of the iron oxide pigments. Synthetic iron oxide pigments are produced industrially on a large scale by solid-state processes, precipitation processes and by the Laux process. Main advantages of synthetic iron oxide pigments compared with natural types are their pure hue, the consistent, reproducible quality and their tinting strength. Iron oxide pigments are mainly used in construction materials, paints, coatings, and plastics, but also in cosmetics, pharmaceuticals and special applications such as ceramics, magnetic coatings and toners.

Induction of Axonal Outgrowth in Mouse Hippocampal Neurons via Bacterial Magnetosomes.

Magnetosomes are membrane-enclosed iron oxide crystals biosynthesized by magnetotactic bacteria. As the biomineralization of bacterial magnetosomes can be genetically controlled, they have become promising nanomaterials for bionanotechnological applications. In the present paper, we explore a novel application of magnetosomes as nanotool for manipulating axonal outgrowth via stretch-growth (SG). SG refers to the process of stimulation of axonal outgrowth through the application of mechanical forces. Thanks to their superior magnetic properties, magnetosomes have been used to magnetize mouse hippocampal neurons in order to stretch axons under the application of magnetic fields. We found that magnetosomes are avidly internalized by cells. They adhere to the cell membrane, are quickly internalized, and slowly degrade after a few days from the internalization process. Our data show that bacterial magnetosomes are more efficient than synthetic iron oxide nanoparticles in stimulating axonal outgrowth via SG.

Value Addition to Ilmenite Using Carbonized Waste Coconut Shells: a Mechanochemical Approach Aided with Powdered Seashells as a Rate Raiser

The value addition potential of ilmenite was examined using several characterization techniques. Raw ilmenite is composed of 93.65 wt.% of FeOTiO2, 3.55 wt.% of SiO2, 1.22 wt.% of Al2O3, and the remainder being other minor oxides. Ilmenite and powdered carbonized coconut shells were mixed in the weight ratio of 4:1. A separate fraction of the same mixture was added with powdered seashells in the weight ratio of 4:1:0.5. Six fractions of each mixture were distinctly milled from 1 to 6 h in a planetary ball mill. XRD spectra (broadened and diminished reflections of ilmenite) and FTIR observations (Ti―O―C bonding) of milled samples indicate the possible incorporation of carbon into the ilmenite structure. Any clues of an occurrence of new rutile peaks were not observed in XRD spectra of milled samples. Consequently, the carbothermic reduction has not been initiated during mechanical activation. In this case, samples powdered for 6 h in a mill were isothermally annealed for 2 h under normal airflow at temperatures of 800 °C, 1000 °C, and 1200 °C, respectively. According to the X-ray diffractograms, the annealing temperatures of 1000 °C and 1200 °C exhibited almost similar trends with rutile (R), pseudobrookite (PB) and elemental iron (F), and a very few ilmenite (I) peaks. Consequently, 6 h of milling and 1000 °C annealing were concluded as the optimum conditions for the carbothermic reduction. Moreover, this study indicated seashells as a potential rate raiser for the carbothermic reduction of ilmenite at 800 °C. Therefore, this process is applicable to upgrade ilmenite into a mixture of synthetic rutile and elemental iron.

Application of Novel Microorganism-Based Formulations as Alternative to the Use of Iron Chelates in Strawberry Cultivation

The strawberry is a low-growing, herbaceous perennial plant, sensitive to iron deficiency. The iron deficiency represents a nutritional disorder, leading to a decreased content of photosynthetic pigments, which determines the yellow color characteristic of chlorotic leaves. Therefore, in calcareous soils, the use of synthetic iron chelate is often mandatory in strawberry cultivation. The employment of novel microorganism-based formulations as alternatives to the use of iron chelates, was evaluated during strawberry cultivation by monitoring the morpho-biometric parameters, chlorophylls, the iron content in leaves and roots, and the Fe chelate reductase activity involved in absorption of iron during the chlorosis event in plants using the strategy I. The experimental design envisaged growing strawberry seedlings on an inert substrate (pumice), irrigated with Hoagland solution iron-free, with a 12 h photoperiod. After 42 days, at the first appearance of chlorosis symptoms, plants were transplanted into a calcareous soil, and after seven days, they were treated, by a single application, with a microorganism-based formulations (MBF), an inoculum (In) of Trichoderma spp. and Streptomyces spp., or Sequestrene (Sq). Strawberry plants were sampled and analyzed at 5, 10, 15, and 20 days from the treatments. The results showed that microorganism-based formulations positively affected the strawberry seedlings, by reducing the chlorosis symptoms, producing comparable effects to the Sequestrene treatment.

Leonardite iron humate and synthetic iron chelate mixtures in Glycine max nutrition.

The aim of this work was to study the possible synergic effect between mixtures with iron leonardite humate (L/Fe3+ ) and synthetic chelates iron (Ch/Fe3+ : o,oEDDHA /Fe3+ or HBED/Fe3+ ), and to reevaluate the classical chelate shuttle-effect model. Different molar ratios of L/Fe3+ :Ch/Fe3+ , different doses, and different sampling times were used in hydroponic and soil experiments using soybean (Glycine max) as a model Strategy I crop in calcareous conditions. Ligand competition between the humate and chelating agents was also examined. Iron humate participates in the chelate shuttle mechanism, providing available Fe to the chelating agent and then to the plants, showing a slight synergic effect. After a few days, the contribution of the chelates to the Fe nutrition decreases substantially, but the contribution of the humates is maintained. The most efficient ratio was two parts of iron humates and one part of iron chelate. In particular, HBED/Fe3+ was the most suitable iron chelate because its lasting effect fits the iron humate long-term effect better. The soluble iron in soil increased and the shoot-to-root iron translocation improved due to a synergic effect by a shuttle effect exerted by iron chelate in the mixture. © 2021 Society of Chemical Industry.

НАНОМАТЕРИАЛЫ В ТЕПЛОВЫХ РЕЗЕРВНЫХ ИСТОЧНИКАХ ТОКА

The current-voltage characteristics of thermal batteries with anodes based on lithium and its alloys, with cathodes made of iron or cobalt disulfides are presented. The electrolyte-melt is a thickened mixture of fluorides, lithium and potassium chlorides, pyrotechnic mixtures of iron, molybdenum, titanium nanopowders. It is shown that the use of a lithium-boron composite and a “thickened lithium” composite is promising as a material for anodes of high-energy thermal current sources, and for cathodes - a mixture based on synthetic iron disulfide.

Evaluation of anti anemic prospective of natural iron sources in lactating women- an ignored important segment of Pakistani population

Abstract Almost entire segment of expecting and breastfeeding mothers in Pakistan are severely affected by iron deficiency anemia (IDA) with predictable prevalence of 50% and as severe public health problem in lactating mothers, has worldwide pervasiveness. Commonly used synthetic iron sources provoke complications. Thus, food sources are preferred due to high bioavailability and sustainability. The present study was done on various natural and synthetic iron sources evaluated for proximate composition, mineral matter, sensory attributes and storage stability. The treatments were fed for 90 days and their efficacy was tested among anemic lactating women. The blood samples of 862 women were taken to examine their hemoglobin level and pertinent biomarkers. Hence, 37.00% volunteers were found to be anemic (Hb < 11 g/dL) and 67.71% women showed IDA problem. Finally, 200 volunteers were strewn arbitrarily into 4 groups. All treatments provided 50% RDA of iron. Dietary intakes and biochemical investigations of T2 group showed momentous improvement (P < 0.05) while linear variations were recorded in anthropometrics, liver function tests (LFTs) and renal function tests (RFTs). Study revealed that food iron sources are easily accessible, cheaper, safe and has more bioavailable iron in skirmishing IDA among lactating women on sustained basis.

Single-Step Sulfur Insertions into Iron Carbide Carbonyl Clusters: Unlocking the Synthetic Door to FeMoco Analogues.

The one-step syntheses, X-ray structures, and spectroscopic characterization of synthetic iron clusters, bearing either inorganic sulfides or thiolate with interstitial carbide motifs, are reported. Treatment of iron carbide carbonyl clusters [Fen (μn -C)(CO)m ]x (n=5,6; m=15,16; x=0,-2) with electrophilic sulfur sources (S2 Cl2 , S8 ) results in the formation of several μ4 -S dimers of clusters, and moreover, iron-sulfide-(sulfocarbide) clusters. The core sulfocarbide unit {C-S}4- serves as a structural model for a proposed intermediate in the radical S-adenosyl-L-methionine biogenesis of the M-cluster. Furthermore, the electrophilic sulfur strategy has been extended to provide the first ever thiolato-iron-carbide complex: an analogous reaction with toluylsulfenyl chloride affords the cluster [Fe5 (μ5 -C)(SC7 H7 )(CO)13 ]- . The strategy described herein provides a breakthrough towards developing syntheses of biomimetic iron-sulfur-carbide clusters like FeMoco.

Single‐Step Sulfur Insertions into Iron Carbide Carbonyl Clusters: Unlocking the Synthetic Door to FeMoco Analogues

AbstractThe one‐step syntheses, X‐ray structures, and spectroscopic characterization of synthetic iron clusters, bearing either inorganic sulfides or thiolate with interstitial carbide motifs, are reported. Treatment of iron carbide carbonyl clusters [Fen(μn‐C)(CO)m]x (n=5,6; m=15,16; x=0,−2) with electrophilic sulfur sources (S2Cl2, S8) results in the formation of several μ4‐S dimers of clusters, and moreover, iron‐sulfide‐(sulfocarbide) clusters. The core sulfocarbide unit {C−S}4− serves as a structural model for a proposed intermediate in the radical S‐adenosyl‐L‐methionine biogenesis of the M‐cluster. Furthermore, the electrophilic sulfur strategy has been extended to provide the first ever thiolato‐iron‐carbide complex: an analogous reaction with toluylsulfenyl chloride affords the cluster [Fe5(μ5‐C)(SC7H7)(CO)13]−. The strategy described herein provides a breakthrough towards developing syntheses of biomimetic iron‐sulfur‐carbide clusters like FeMoco.

Simultaneous removal of Cr(VI), Cd, and Pb from aqueous solution by iron sulfide nanoparticles: Influencing factors and interactions of metals

• Cr(VI), Cd, and Pb may be removed from aqueous solutions simultaneously by FeS NPs. • Acidic pH values favor Cr(VI) removal, and alkaline pH values favor Cd and Pb removal. • Oxygen inhibits Cr(VI) removal, but does not influence Cd and Pb removal. • The interactions between Cr(VI), Cd, and Pb involve enhanced adsorption and precipitation. Cadmium (Cd), lead (Pb), and hexavalent chromium (Cr(VI)) are often found in soils and water affected by metal smelting, chemical manufacturing, and electroplating. In this study, synthetic iron sulfide nanoparticles (FeS NPs) were stabilized with carboxymethyl cellulose (CMC) and utilized to remove Cr(VI), Cd, and Pb from an aqueous solution. Batch experiments, a Visual MINTEQ model, scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectrometer (XPS) analysis were used to determine the removal efficiencies, influencing factors, and mechanisms. The FeS NP suspension simultaneously removed Cr(VI), Cd, and Pb from an aqueous solution. The concentrations of Cr(VI), Cd, and Pb decreased from 50, 10, and 50 mg·L −1 to 2.5, 0.1, and 0.1 mg·L −1 , respectively. The removal capacities were up to 418, 96, and 585 mg per gram of stabilized FeS NPs, respectively. The acidic conditions significantly favored the removal of aqueous Cr(VI) while the alkaline conditions favored the removal of Cd and Pb. Oxygen slightly inhibited the removal of Cr(VI), but it had no significant influence on the removal of Cd and Pb. A potential mechanism was proposed for the simultaneous removal of Cr(VI), Cd, and Pb using FeS NPs. The interactions of the three heavy metals involved a cationic bridging effect on Cr(VI) by Cd, an enhanced adsorption effect on Cd by [Cr,Fe](OH) 3 , precipitation of PbCrO 4 , and transformation of PbCrO 4 to PbS. Therefore, FeS NPs have a high potential for use in the simultaneous removal of Cr(VI), Cd, and Pb from contaminated aqueous solutions.