Presence Of Reductant Research Articles

A Dinitrogen Divanadium Complex Supported by a Trisamidophosphine Ligand

Comprehensive SummaryThe reaction between tripodal trisamidophosphine ligand H3PN3Ar and V(Mes)3(THF) (Mes = mesityl) yields the vanadium(III) complex (PN3Ar)V (1) with an open site in the axial position, which could coordinate with THF, pyridine, and NH3 to form the corresponding adducts (2—4). The vanadium(III) center is redox‐active, as demonstrated by cyclic voltammetry methods and chemical oxidation or reduction. Notably, a novel dinitrogen divanadium complex with a bridging N2 ligand, {K(THF)}2{[PN3Ar]V}2(μ‐N2) (6), was synthesized via treatment of 1 with 1 equivalent of potassium naphthalenide in THF under a N2 atmosphere. The electronic structures and binding properties of 6 are evaluated and discussed based on its DFT calculations. Additionally, these vanadium complexes (1, 5, 6) can serve as catalysts for the conversion of N2 into N(SiMe3)3 in the presence of reductants and Me3SiCl.

SARS-CoV-2 accessory protein 7b forms homotetramers in detergent

A global pandemic is underway caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The SARS-CoV-2 genome, like its predecessor SARS-CoV, contains open reading frames that encode accessory proteins involved in virus-host interactions active during infection and which likely contribute to pathogenesis. One of these accessory proteins is 7b, with only 44 (SARS-CoV) and 43 (SARS-CoV-2) residues. It has one predicted transmembrane domain fully conserved, which suggests a functional role, whereas most variability is contained in the predicted cytoplasmic C-terminus. In SARS-CoV, 7b protein is expressed in infected cells, and the transmembrane domain was necessary and sufficient for Golgi localization. Also, anti-p7b antibodies have been found in the sera of SARS-CoV convalescent patients. In the present study, we have investigated the hypothesis that SARS-2 7b protein forms oligomers with ion channel activity. We show that in both SARS viruses 7b is almost completely α-helical and has a single transmembrane domain. In SDS, 7b forms various oligomers, from monomers to tetramers, but only monomers when exposed to reductants. Combination of SDS gel electrophoresis and analytical ultracentrifugation (AUC) in both equilibrium and velocity modes suggests a dimer-tetramer equilibrium, but a monomer–dimer–tetramer equilibrium in the presence of reductant. This data suggests that although disulfide-linked dimers may be present, they are not essential to form tetramers. Inclusion of pentamers or higher oligomers in the SARS-2 7b model were detrimental to fit quality. Preliminary models of this association was generated with AlphaFold2, and two alternative models were exposed to a molecular dynamics simulation in presence of a model lipid membrane. However, neither of the two models provided any evident pathway for ions. To confirm this, SARS-2 p7b was studied using Planar Bilayer Electrophysiology. Addition of p7b to model membranes produced occasional membrane permeabilization, but this was not consistent with bona fide ion channels made of a tetrameric assembly of α-helices.

Iron Extraction from South African Ilmenite Concentrate Leaching by Hydrochloric Acid (HCl) in the Presence of Reductant (Metallic Fe) and Additive (MgSO4)

The high content of iron in ilmenite ore poses a great challenge, particularly in the synthesis of titanium-containing products due to high susceptibility of iron (Fe) to corrosion. Direct leaching of ilmenite ore in hydrochloric acid (HCl) encouraging Fe dissolution was investigated. The influence of variable parameters, the use of additives, and the addition of metallic iron powder were studied to establish the optimum leaching parameters. The results showed that ilmenite with the particle size distribution of +150 µm yielded better efficiencies when leaching was performed with an acid concentration of 7.5 M and a solid-to-acid ratio of 1:10 at 90 °C. An agitation speed of 450 rpm yielded a superior Fe extraction of about 92.32% and a 2.40% titanium (Ti) loss. The addition of both metallic Fe and the MgSO4 additive significantly enhanced Fe dissolution and decreased Ti recovery in a leach solution. It was found that leaching under optimum conditions produced a solid residue with 1.37% Fe impurity while 98.63% was extracted. The leached residue was comprised of 91.4% TiO2 rutile phase and contained a high content of the ilmenite FeTiO3 (4.37%) and SiO2 (2.23%) impurities, while Al2O3, MgO, MnO2, CaO, V2O5, MnO2, and Cr2O3 were below 0.13%. The high TiO2 content in the leached residue makes it suitable for use as feed in the production of synthetic rutile. The leaching kinetics of Fe dissolution was found to conform to the shrinking core model, where diffusion through the product layer is rate controlling. The calculated activation energy according to the Arrhenius equation was 19.13 kJ/mol.

Non-Pathogenic bacteria in Bioremediation of Cr (VI) for decontamination of ground water: An Extensive Review

Cr(VI), one of the most common ground waters heavy metal contaminant due to its indiscriminateuse in different industries has become a matter of major environmental concern. So, it is desirable that remediation methods should be such that brings its level within the permissible limits before effluents are discharged. The methods should be cheap as well as eco-friendly. Nowadays, severalbiological remediation strategies are used by applying microorganisms for its removal involving biosorption and biotransformation. Biosorption is dependent on surface nature of the biosorbentswhereas biotransformations depend on the presence of reductants. The present review includes bioremediation strategies of Cr(VI) based on biosorption or biotransformation or both by non-pathogenic bacteria only.

Membrane‐Bound Inward‐Growth of Artificial Cytoskeletons and Their Selective Disassembly

AbstractThe cytoskeleton is one of the most important cellular components. Up to now, most of the reported artificial cytoskeletons are based on a gel‐in‐vesicle strategy. Herein, we report a membrane‐bound inward‐growth pathway to prepare cytoskeleton‐like and radially aligned nanofibers grown from capsule membranes to get membrane‐bound artificial cytoskeletons (MACs). The mechanism therein is disclosed through the direct observation of the intermediates in both dried and liquid states. Furthermore, the as‐prepared MACs show a selective disassembly behavior in the presence of reductants: both capsule membranes and MACs can be disassembled or only MACs can be disassembled through the selective introduction of dynamic disulfide bonds (DS) into them and by the switch of ultraviolet (UV) irradiation. The present work provides a new hierarchical self‐assembly way to construct artificial cytoskeletons with controlled compositions and orientations.

Membrane-Bound Inward-Growth of Artificial Cytoskeletons and Their Selective Disassembly.

The cytoskeleton is one of the most important cellular components. Up to now, most of the reported artificial cytoskeletons are based on a gel-in-vesicle strategy. Herein, we report a membrane-bound inward-growth pathway to prepare cytoskeleton-like and radially aligned nanofibers grown from capsule membranes to get membrane-bound artificial cytoskeletons (MACs). The mechanism therein is disclosed through the direct observation of the intermediates in both dried and liquid states. Furthermore, the as-prepared MACs show a selective disassembly behavior in the presence of reductants: both capsule membranes and MACs can be disassembled or only MACs can be disassembled through the selective introduction of dynamic disulfide bonds (DS) into them and by the switch of ultraviolet (UV) irradiation. The present work provides a new hierarchical self-assembly way to construct artificial cytoskeletons with controlled compositions and orientations.

Ferrate(VI) pretreatment of water containing natural organic matter, bromide, and iodide: A potential strategy to control soluble lead release from PbO2(s)

Lead dioxide (PbO2(s)) is a corrosion product of lead-containing plumbing materials in water distribution pipelines. The presence of reductants in water could cause the release of soluble lead (mainly Pb(II)) from PbO2(s). Lead in drinking water is detrimental to public health. This paper presents the first application of ferrate (FeVIO42−, Fe(VI)) to decreasing the generation of soluble lead in water containing PbO2(s) and common reducing constituents (e.g., natural organic matter (NOM), iodide (I−), and bromide (Br−)) at different pH conditions (i.e., 6.0, 7.0, and 8.0). The released soluble lead from PbO2(s) was found to be dominantly controlled by NOM in water, via the redox dissolution of PbO2(s) and the reduction of PbO2(s) by reducing moieties of NOM. The feasibility of both processes increased when pH decreased. The I− and Br− in water played minor roles in generating soluble lead. Fe(VI) reacted with reducing functional groups of NOM, as determined by 13C nuclear magnetic resonance spectroscopy. Water pretreatment with Fe(VI) inhibited the reaction of NOM with PbO2(s) and therefore, caused lower soluble lead concentrations compared to water samples without Fe(VI) treatment. This study indicates that Fe(VI) pretreatment is a potential approach to controlling soluble lead in drinking water.

A General Mechanism of Green-to-Red Photoconversions of GFP.

Here we dissect the phenomena of oxidative and reductive green-to-red photoconversion of the Green Fluorescent Protein. We characterize distinct orange- and red-emitting forms (λabs/λem = 490/565 nm; λabs/λem = 535/600 nm) arising during the Enhanced Green Fluorescent Protein (EGFP) photoconversion under low-oxygen conditions in the presence of reductants. These forms spectroscopically differ from that observed previously in oxidative redding (λabs/λem = 575/607 nm). We also report on a new green-emitting state (λabs/λem = 405/525 nm), which is formed upon photoconversion under the low-oxygen conditions. Based on the spectral properties of these forms, their light-independent time evolution, and the high-level computational studies, we provide a structural basis for various photoproducts. Under the low-oxygen conditions, the neutral quinoid-like structure formed via a two-electron oxidation process is found to be a key intermediate and a most likely candidate for the novel green-emitting state of the chromophore. The observed large Stokes shift is traced to the formation of the zwitterionic form of the chromophore in the excited state. Subsequently, this form undergoes two types of cyclization reactions, resulting in the formation of either the orange-emitting state (λabs/λem = 490/565 nm) or the red-emitting form (λabs/λem = 535/600 nm). The T65G mutant lacks one of the proposed cyclization pathways and, indeed, the photoconverted T65G EGFP exhibits a single orange-emitting state. In oxidative redding, the red-emitting state resembles the structure of the chromophore from asFP595 (λabs/λem = 572/595 nm), which is directly formed upon two-electron oxidation and deprotonation bypassing the formation of the quinoid-like structure. Our results disclose a general “oxidative” mechanism of various green-to-red photoconversions of EGFP, providing a link between oxidative redding and the photoconversion under low-oxygen conditions.

Reduced graphene oxide supported palladium nano-shapes for electro-oxidation of oxalic acid

Size & shape controlled synthesis of metal nanoparticles are of high importance in catalysis. Colloidal techniques offer fine tunings in synthesis process as it involve multiple steps and reaction parameters. An efficient way of producing morphology controlled palladium nanostructures viz. palladium nanocubes (Pd-nc), palladium nanoicosahedrons (Pd-nico) supported on reduced graphene oxide (rGO) and its application in electro-catalysis is reported here. These Pd nano-shapes were achieved via sequential chemical reduction of Pd metal precursor and graphene oxide in the presence of reductant, ethylene glycol (EG) and stabilizer (capping agent), polyvinylpyrrolidone (PVP). Potassium bromide (KBr) and ascorbic acid (AA) were used as structure directing and secondary reducing agents respectively, to tune the geometry of Pd nanoparticles (Pd NPs). The preparation steps were optimized to yield cube shaped Pd nanoparticles (Pd-nc) with mean diameter of 4nm in the presence of KBr/AA; while in their absence, icosahedron shaped Pd nanoparticles (Pd-nico) with mean diameter of 3.1nm were formed and then homogeneously distributed over rGO sheets as evidenced by SEM-EDX and TEM. Further, Pd-nc/rGO and Pd-nico/rGO hybrid composite materials were used to investigate the electrochemical oxidation of oxalic acid (OA) in acidic medium. The results reveal that, these optimal size ranged nanostructures exhibit enhanced electro-catalytic activity when compared to bare glassy carbon electrode (GCE), towards OA oxidation. Among the two, Pd-nico/rGO showed enhanced activity than Pd-nc/rGO. The activity difference was justified based on the particle size distribution and no of surface exposed sites. The synthesis approach provides a versatile route for morphology (shape and size) controlled synthesis of metal nanostructures immobilized on support materials aiming towards fabrication of low cost composites in electro-catalysis and potential sensor applications.

Biochar-supported magnetic noble metallic nanoparticles for the fast recovery of excessive reductant during pollutant reduction

The catalytic reduction of diverse pollutants by noble metal catalysts in the presence of reductants is a highly effective and widely used method. However, the considerable cost of noble metal catalysts impedes the practical application of this method, and the recovery of excessive reductants has not been reported previously. In this work, we prepared inexpensive biochar-supported magnetic noble metallic nanoparticles (NPs) and efficiently recovered the excessive reductants in the form of H2. The as-synthesized biochar-supported noble metallic NPs exhibited high H2 recovery during the 4-nitrophenol reduction reaction. Results showed that the catalysts with low noble metallic content have higher H2 recovery rate than commercial Pd/C, Ag/C, and Pt/C. The catalytic mechanism of magnetic biochar-supported noble metallic NPs was demonstrated to be a “synergetic effect”, where biochar and Fe3O4 acted as accelerants that enable noble metallic NPs to produce active hydrogen for the reduction reaction, and the excess active hydrogen atoms combined to form H2.

Transition Metal‐Catalyzed Reductive Functionalization of CO2

Reductive functionalization of CO2 combining both the formation of the new bonds and CO2 reduction in the presence of reductant, such as molecular hydrogen, hydrosilane, or hydroborane has become increasingly attractive, which enlarges the spectra of compounds directly available from CO2 thus provides fresh idea for CO2 chemistry. This microreview briefly summarizes recent advances in new bond construction using CO2 as formyl, methylene, and methyl source with transition‐metal catalyst, which are divided into sections according to C–N, C–C, and C–O bonds formation in the presence of nitrogen‐, carbon‐, and oxygen‐nucleophiles respectively. The challenges and opportunities with future trends of the reductive functionalization of CO2 are discussed as well.

Silver Nanoparticles Formed in a Colloidal System and a Polymer Matrix

The growth kinetics and particle-size distribution of Ag particles in a polyvinyl alcohol (PVA) composite, PVA film, and aqueous sol were studied using UV and visible spectroscopy, atomic force microscopy, and dynamic light scattering. A hypsochromic shift (55 nm) of the Ag nanoparticle (NP) surface plasmon absorption maximum was measured on going from the PVA composite to the film. The kinetics of Ag NP formation and their sizes were shown to depend considerably on UV irradiation, ultrasound action, and PVA concentration. It was established that UV irradiation accelerated Ag NP formation in the presence of reductants and destroyed the resulting NPs with a deficit of reductant. Partial destruction of the Ag NPs occurred under the influence of ultrasound whereas ultrasound action after UV irradiation reduced Ag+ on the clusters.

Perrhenate-Catalyzed Deoxydehydration of a Vicinal Diol: A Comparative Density Functional Theory Study.

Oxo-rhenium compounds, such as perrhenate salts, have demonstrated preferable activity in catalyzing the deoxydehydration (DODH) reaction in the presence of reductants. Here, the first computational details of the reported DODH mechanisms are presented using the density functional theory (DFT) (M06/6-311+G(d,p)/LANL2DZ) to investigate the conversion of a vicinal diol into the corresponding alkene by ReO4- as a catalyst. The DFT studies were carried out to evaluate the DODH mechanisms, from the energy point of view, for the conversion of phenyl-1,2-ethanediol to styrene by perrhenate anion in the presence of PPh3 as a reductant through a detailed comparison of two potential pathways including pathway A and pathway B. Pathway A includes the sequence of condensation of oxo-Re(VII) with diol before the reduction of Re(VII) to Re(V), whereas pathway B involves the reduction of oxo-Re(VII) to oxo-Re(V) before the condensation process. In pathway B, two basic routes (B1 and B2) are possible, which can take place through different reaction steps, including the extrusion of alkene from Re(V)-diolate in route B1, and the second reduction of the Re(V)-diolate by reductant and then the extrusion of alkene from the Re(III)-diolate intermediate in route B2. The intermediates and the Gibbs free energy changes, including ΔG°g and ΔG°sol, have been calculated for alternative pathways (A and B) in the gas and solvent (chlorobenzene and methanol) phases and compared to each other. In addition, the transition states and the activation energy barriers for two pathways (A and B) in the gas phase and in chlorobenzene have been calculated. The key transition states include the nucleophilic attack of PPh3 on an Re═O bond, the dissociation of OPPh3 from the rhenium moiety, the transfer of an H atom of diol to the oxo ligand in an oxo-Re bond through the condensation step, and the extrusion of styrene from the Re-diolate complexes. The DFT results indicate that the DODH reaction is thermodynamically feasible through both pathways (A and B). However, the calculations reveal that the perrhenate-catalyzed DODH reaction through pathway A has the lowest overall activation barrier energy among the DODH mechanism routes.

Rapid Visible Light-Mediated Controlled Aqueous Polymerization with In Situ Monitoring.

We report a simple procedure for rapid, visible light-mediated, controlled radical polymerization in aqueous solutions. Based on the photoelectron transfer reversible addition-fragmentation chain transfer (PET-RAFT) polymerization, fast chain propagation at room temperature in water was achieved in the presence of reductant and without prior deoxygenation. A systematic study correlating irradiation intensity and polymerization kinetics, enabled by in situ nuclear magnetic resonance spectroscopy, provided optimized reaction conditions. The versatility of this procedure was demonstrated through a rapid triblock copolymer synthesis, and incorporation of water-labile activated esters for direct conjugation of hydrophilic small molecules and proteins. In addition, this technique boasts excellent temporal control and provides a wide range of macromolecular materials with controlled molecular weights and narrow molecular weight distributions.

Deoxygenation of Ethers To Form Carbon-Carbon Bonds via Nickel Catalysis.

In this article a successful protocol was developed to construct carbon-carbon bonds by the extrusion of the O atom of ethers via nickel catalysis in the presence of reductants. This methodology is featured as a highly economic route to construct sp3-sp3 C-C bonds through dual C-O activation of ethers with good functional group tolerance.

Trans-membrane Signaling in Photosynthetic State Transitions: REDOX- AND STRUCTURE-DEPENDENT INTERACTION IN VITRO BETWEEN STT7 KINASE AND THE CYTOCHROME b6f COMPLEX

Trans-membrane signaling involving a serine/threonine kinase (Stt7 in Chlamydomonas reinhardtii) directs light energy distribution between the two photosystems of oxygenic photosynthesis. Oxidation of plastoquinol mediated by the cytochrome b6f complex on the electrochemically positive side of the thylakoid membrane activates the kinase domain of Stt7 on the trans (negative) side, leading to phosphorylation and redistribution ("state transition") of the light-harvesting chlorophyll proteins between the two photosystems. The molecular description of the Stt7 kinase and its interaction with the cytochrome b6f complex are unknown or unclear. In this study, Stt7 kinase has been cloned, expressed, and purified in a heterologous host. Stt7 kinase is shown to be active in vitro in the presence of reductant and purified as a tetramer, as determined by analytical ultracentrifugation, electron microscopy, and electrospray ionization mass spectrometry, with a molecular weight of 332 kDa, consisting of an 83.41-kDa monomer. Far-UV circular dichroism spectra show Stt7 to be mostly α-helical and document a physical interaction with the b6f complex through increased thermal stability of Stt7 secondary structure. The activity of wild-type Stt7 and its Cys-Ser mutant at positions 68 and 73 in the presence of a reductant suggest that the enzyme does not require a disulfide bridge for its activity as suggested elsewhere. Kinase activation in vivo could result from direct interaction between Stt7 and the b6f complex or long-range reduction of Stt7 by superoxide, known to be generated in the b6f complex by quinol oxidation.

Urchin-like Cobalt Nanostructures For Catalytic Degradation Of Nitro Anilines

The undertaken study describes synthesis of urchin-like Cobalt nanostructures (Co NSs) in aqueous solution using gallic acid as both reductant and protecting agent for the catalytic degradation of 4-methyle-2-nitroaniline. UV-Visible (UV-Vis) spectroscopy was used as a primary tool to elaborately study and optimizes the necessary experimental condition for the developed synthetic protocol Fourier transform infrared (FTIR) spectroscopy showed the interaction between gallic acid and the surface of Co NSs via -OH linkages although Scanning electron microscopy (SEM) confirmed the formation of urchin shaped nanostructures with diameter in the range of 80-110 nm and length of tentacles between 1.0 - 1.8 µm. The as-synthesized Co NSs proved to be excellent heterogeneous catalyst for the 100 % reductive degradation of 4-methyle-2-nitroaniline in just 60 sec in presence of reductant (NaBH4) with reaction rate calculated to follow pseudo first order kinetic and rate constant of 0.055s -1 . Furthermore, Co NSs, showed excellent recyclability and were reused four times for the degradation of 4-methyle-2- nitroaniline with efficiency that displayed negligible catalytic poisoning. Copyright © 2016 VBRI Press.

Control of light-dependent keto carotenoid biosynthesis in Nostoc 7120 by the transcription factor NtcA.

In Nostoc PCC 7120, two different ketolases, CrtW and CrtO are involved in the formation of keto carotenoids from β-carotene. In contrast to other cyanobacteria, CrtW catalyzes the formation of monoketo echinenone whereas CrtO is the only enzyme for the synthesis of diketo canthaxanthin. This is the major photo protective carotenoid in this cyanobacterium. Under high-light conditions, basic canthaxanthin formation was transcriptionally up-regulated. Upon transfer to high light, the transcript levels of all investigated carotenogenic genes including those coding for phytoene synthase, phytoene desaturase and both ketolases were increased. These transcription changes proceeded via binding of the transcription factor NtcA to the promoter regions of the carotenogenic genes. The binding was absolutely dependent on the presence of reductants and oxo-glutarate. Light-stimulated transcript formation was inhibited by DCMU. Therefore, photosynthetic electron transport is proposed as the sensor for high-light and a changing redox state as a signal for NtcA binding.

Hydrothermal synthesis of CoSe nanostructures without using surfactant

CoSe nanostructures are synthesized by hydrothermal route in the presence of reductant, without using surfactant. In this work, we use from SeCl4 as a new selenium source. By varying the type of metal salt and reductant, reaction time and temperature, the method permits us to synthesize products with different morphologies. SEM and TEM images show the morphology and size of the as-synthesized samples. Chemical composition of the samples is characterized by XRD and EDS. Magnetization measurement shows paramagnetic behavior for CoSe nanostructures.

Imaging the reduction of chromium(VI) on magnetite surfaces using in situ electrochemical AFM

Hexavalent chromium is a highly toxic and readily mobile metal contaminant introduced to the environment through a variety of industrial operations. In the presence of reductants, such as Fe(II), and catalytic mineral surfaces, such as iron oxides surfaces, Cr(VI) may be reduced to a less toxic and relatively insoluble form Cr(III). In this study, we investigate the interaction between Cr(VI) and the surface of the Fe(II)-bearing mineral magnetite, Fe(II)Fe(III)2O4, as an example catalyst, using electrochemical atomic force microscopy (EC-AFM). With this method, the redox potential is controlled by an electrode, and Cr deposition on the magnetite surface is imaged over time as a function of redox potential and pH of the solution. Quantitative analyses of volumetric growth and surface coverage reveal that more precipitation occurs over time at very negative (−500mV at pH3, −750mV at pH7, and −1000mV at pH11) and very positive (+1000mV at pH3 and +500mV at pH11) electrochemical potentials. Up to 70% of the surface is covered with precipitates at pH7, while less coverage is observed at pH11 (<8%) and pH3 (<2%). Particle growth at pH3 is predominantly lateral in nature with a tendency to form a higher number of smaller adsorbate particles. At pH11, growth is primarily vertical (perpendicular to the surface), and smaller particles tend to aggregate into larger clusters on the surface with increasingly negative redox polarization. These larger clusters (most likely subcrystalline Cr-(oxy)hydroxides) co-exist with rhombic, crystalline particles that likely have preferred crystallographic growth relationships with the magnetite substrate; the composition of this latter type of particle is most likely chromite, FeCr2O4, based on the matching crystallography and stability under the Eh/pH conditions of this experiment.Results from growth analyses were confirmed by batch experiments performed on the same samples used in the AFM, where changes in the Cr concentration in solution were monitored using inductively coupled plasma mass spectrometry (ICP-MS). Virtually all of the Cr was removed after 30min at pH7 (starting at 2μM Cr(VI)) at all potentials, ~60% at pH3, and very little removal at pH11. X-ray photoelectron spectroscopy (XPS) analyses of the magnetite surface at pH3 suggest that only Cr(III) phases are present and that Cr and/or Fe–Cr oxide phases are more stable at very reducing conditions (−750mV), while Cr and/or Fe–Cr (oxy)hydroxide phases are present under more moderately-reducing conditions (−250mV). At pH11, any Cr deposited is below the detection limit for XPS analysis (<1% surface coverage); however, Fe(II)/Fe(III) ratios (~0.3) are lower than the expected ratio of magnetite, which indicates that some oxidation of the surface has occurred. This oxidized layer, possibly maghemite (γ-Fe2O3), hematite (α-Fe2O3), or FeOOH, may inhibit the reduction of Cr(VI) on the surface.