Presence Of Nitrilotriacetic Acid Research Articles

The role of ligand in the activation of peroxymonosulfate by Fe3O4 for the degradation of organic pollutants

Advanced oxidation processes based on peroxymonosulfate (PMS) hold remarkable promise for addressing emerging organic pollutants (EOPs) and are worthy of systematic investigation. However, the existing technology has not been widely applied due to bottlenecks such as reaction efficiency. Herein, we proposed a novel system incorporating nitrilotriacetic acid (NTA) as a functional ligand to enhance the activation of PMS by Fe3O4, thereby facilitating a better efficiency for the degradation of EOPs. Results indicated that the system can achieve an optimal removal rate of 99.6% for atrazine (ATZ) in the presence of NTA. Quenching experiments and electron paramagnetic resonance techniques were employed for mechanism exploration. The results revealed that the enhanced Fe(II)/Fe(III) cycling on the surface of Fe3O4, triggered by the addition of NTA, accelerates the reduction of trivalent iron and continuously activates PMS to generate radicals, particularly SO4−. The mechanistic analysis showed that in the first stage, the lower degradation efficiency could due to the self-quenching of the free radicals, with the uncomplexed Fe(II) and Fe(III) on the surface, the free NTA in the solution, or with the PMS, in addition to reacting with the pollutants. In the second stage, the ATZ achieved rapid degradation as the concentration of substances competing for free radicals decreased. Our work elucidates the key role of NTA functional ligand in the Fe3O4/PMS advanced oxidation processes, which may provide new approach for the efficient degradation of EOPs.

Enhanced removal of sulfamethoxazole by Mn(II)/bisulfite in presence of nitrilotriacetic acid: Role of Mn(III)

Currently, the research on bisulfite (BS) activation by Mn(II) is very limited probably because of the low catalytic efficiency of Mn(II). Adding ligands to Mn(II)/BS system is likely to improve the BS activation, but the relative information is very rare. Therefore, the effect of nitrilotriacetic acid (NTA) on Mn(II)/BS system was investigated in this work using sulfamethoxazole (SMX) as the target contaminant. The results showed that the addition of NTA enhanced SMX removal in Mn(Ⅱ)/BS system through forming Mn(Ⅱ/III)-NTA complexes driving Mn(III)/Mn(II) cycle and stabilizing Mn(III). Alcohol scavenging experiments and competitive kinetic experiments indicated that sulfate radical (SO4•−) and hydroxyl radical (HO•) were not the main reactive species in Mn(II)/NTA/BS system. Mn(Ⅲ) was the primary oxidant for SMX elimination in this system and its existence was proved by UV-Vis absorption spectrum of reaction solution. Mn(Ⅱ)/NTA/BS system could greatly degrade SMX in near-neutral conditions, while nearly no SMX removal was observed at pH 3.0. The decrease of dissolved oxygen concentration significantly inhibited BS autocatalytic stage, thus suppressing the removal of SMX. Due to the competitive complexation of HCO3− and FA with NTA for Mn(II), their addition in Mn(Ⅱ)/NTA/BS system obviously inhibited SMX degradation. Four intermediates were detected during SMX degradation in Mn(Ⅱ)/NTA/BS system, and the possible SMX transformation pathways were speculated as N-S bond breaking, hydroxylation, amino oxidation and coupling reaction.

Nitrilotriacetic acid-assisted Mn(II) activated periodate for rapid and long-lasting degradation of carbamazepine: The importance of Mn(IV)-oxo species.

Periodate-based (PI, IO4-) oxidation processes for pollutant elimination have gained increased attention in recent years. This study shows that nitrilotriacetic acid (NTA) can assist trace Mn(II) in activating PI for fast and long-lasting degradation of carbamazepine (CBZ) (100% degradation in 2min). PI can oxidize Mn(II) to permanganate(MnO4-, Mn(VII)) in the presence of NTA, which indicates the important role of transient manganese-oxo species. 18O isotope labeling experiments using methyl phenyl sulfoxide (PMSO) as a probe further confirmed the formation of manganese-oxo species. The chemical stoichiometric relationship (PI consumption: PMSO2 generation) and theoretical calculation suggested that Mn(IV)-oxo-NTA species were the main reactive species. The NTA-chelated manganese facilitated direct oxygen transfer from PI to Mn(II)-NTA and prevented hydrolysis and agglomeration of transient manganese-oxo species. PI was transformed completely to stable and nontoxic iodate but not lower-valent toxic iodine species (i.e., HOI, I2, and I-). The degradation pathways and mechanisms of CBZ were investigated using mass spectrometry and density functional theory (DFT) calculation. This study provided a steady and highly efficient choice for the quick degradation of organic micropollutants and broadened the perspective on the evolution mechanism of manganese intermediates in the Mn(II)/NTA/PI system.

Transparent polycarbonate coated with CeO2 nanozymes repel Pseudomonas aeruginosa PA14 biofilms.

Highly transparent CeO2/polycarbonate surfaces were fabricated that prevent adhesion, proliferation, and the spread of bacteria. CeO2 nanoparticles with diameters of 10-15 nm and lengths of 100-200 nm for this application were prepared by oxidizing aqueous dispersions of Ce(OH)3 with H2O2 in the presence of nitrilotriacetic acid (NTA) as the capping agent. The surface-functionalized water-dispersible CeO2 nanorods showed high catalytic activity in the halogenation reactions, which makes them highly efficient functional mimics of haloperoxidases. These enzymes are used in nature to prevent the formation of biofilms through the halogenation of signaling compounds that interfere with bacterial cell-cell communication ("quorum sensing"). Bacteria-repellent CeO2/polycarbonate plates were prepared by dip-coating plasma-treated polycarbonate plates in aqueous CeO2 particle dispersions. The quasi-enzymatic activity of the CeO2 coating was demonstrated using phenol red enzyme assays. The monolayer coating of CeO2 nanorods (1.6 μg cm-2) and the bacteria repellent properties were demonstrated by atomic force microscopy, biofilm assays, and fluorescence measurements. The engineered polymer surfaces have the ability to repel biofilms as green antimicrobials on plastics, where H2O2 is present in humid environments such as automotive parts, greenhouses, or plastic containers for rainwater.

Interactions between copper (II) and β-amyloid peptide using capillary electrophoresis-ICP-MS: Kd measurements at the nanogram scale.

Although the interaction between the β-amyloid peptide and copper (II) appears to play an important role in Alzheimer's disease, the affinity constant is still controversial and values are ranging from 107 to 1011 M-1. With the aim of clarifying this point, a complementary method, based on the capillary electrophoresis-ICP-MS hyphenation, was developed and competitive binding experiments were conducted in the presence of nitrilotriacetic acid. The effect of the capillary surface (neutral or positively charged) and nature of the buffer (Tris or Hepes) have been studied. Tris buffer was found to be inappropriate for such determination as it enhances the dissociation of copper (II) complexes, already occurring in the presence of an electric field in capillary electrophoresis. Using Hepes, a value of 1010 M-1 was found for the affinity of the small β-amyloid peptide 1-16 for copper (II), which is in agreement with the values obtained for other proteins involved in neurodegenerative diseases. These constants were also determined in conditions closer to those of biological media (higher ionic strength, presence of carbonates).

Potentiometric Titration of Vanadium (V) with Iron (II) in the Presence of NTA and DTPA Using Dry-Cell Graphite Electrode

A sensitive potentiometric titration for vanadium (V) based effect of ligands such as nitrilotriacetic acid (NTA) and diethylenetriaminepenta-acetic acid (DTPA) are reviewed. The potential iron system decreased the presence of NTA and DTPA. In this case, iron (III) increased with respect to the vanadium (IV) volume. The production of iron (III)-ligand complex has increased. This result suggested that the formation of V(V)-NTA and V(V)-DTPA complexes were less favoured than that of V(IV)-NTA and V(IV)-DTPA complexes. The calculated correlation coefficients (r) conveyed the effectiveness of the graphite electrode as the indicator electrode for the potentiometric titrations. On comparing the potential jump values, the extent of potential caused by DTPA was found to be more than that of NTA. The utilization of graphite electrode has facilitated the potentiometric titration by significantly causing larger potential jump. This method was precise and accurate as no interference of foreign ions was observed. Hence, the approach could be applied to the vanadium (V) of any samples.

Individual and synergetic effect of EDTA and NTA on polymorphism and morphology of CaCO3 crystallization process in presence of barium

The effect of different chelating agents on the crystallization of CaCO3, polymorphism and morphology of CaCO3 in the presence of barium were studied at 100 °C. The samples were characterized using FTIR, Raman spectroscopy, XRD and FESEM techniques. The study revealed that without any chelating agents, in the presence of different volumes of 0.1 M Ba2+ ion solution, stabilization of a binary mixture of rhombohedral calcite and flower-like vateritewas facilitated. In the presence of EDTA, the phenomenal transformation of calcite to vateritewas observed. Pure calcite has resulted in the presence of Nitrilotriacetic acid (NTA) in the presence of Ba2+ ions. Blending EDTA with NTA favored a binary mixture of spherical vaterite and calcite. The probable mechanism for stabilization of various polymorphs by the additives and effect of blending of additives for better scale inhibition efficiency has been discussed.

Nitrilotriacetic acid enhanced UV/Fe0/H2O2 process for salty wastewater treatment at neutral pH

In this study, nitrilotriacetic acid (NTA) was used to enhance UV/Fe0/H2O2 process for highly salty wastewater at neutral pH. The addition of Fe0 could not accelerate the UV/H2O2 process for salty wastewater treatment at neutral pH due to the precipitation of Fe ions. While NTA added into UV/Fe0/H2O2 process which could form complex with Fe ion, the tartrazine removal could increase from 45.7% to 84.7% within 60 ​min. The k-value of the UV/Fe0-NTA/H2O2 system to remove tartrazine is also 2.2 times higher than that in UV/Fe0/H2O2 system. Meanwhile, the UV/Fe0-NTA/H2O2 process could obtain good performance for salt wastewater treatment under a wide salt concentration level of 0–0.2 ​M. It can also expand the application range of pH to neutral pH. SEM and XPS characterization showed that the corrosion rate of Fe0 in salty system was faster, and the presence of NTA could accelerate the recirculation of Fe3+/Fe2+ on the Fe0 surface. EPR spectroscopic analysis and scavenge experiments showed that •OH was the main reactive radical for the removal of tartrazine in the UV/Fe0-NTA/H2O2 system. In addition, the k-value for removing tartrazine in various types of salt systems in the UV/Fe0-NTA/H2O2 system was 3.2–4.2 times that of the UV/Fe0/H2O2 system. It demonstrated UV/Fe0-NTA/H2O2 processes fits to different types of salt system. Therefore, this study will provide a new method for the treatment of saline wastewater at neutral pH.

Synthesis of a crosslinked poly(ionic liquid) and evaluation of its antimony binding properties

First ever ionic liquid derived sorbent for antimony was synthesised. The charged functional groups of the polymer showed preferential binding and strong affinity for difficult to remove anionic species of antimony. The sorbent was synthesised by crosslinking co-polymerisation of 1-butyl-3-vinylimidazolium bromide with N,N-methylenebis(acrylamide). SEM-EDS analysis showed that the polymer retained the bromide counter ions. Antimony removal properties under wide solution conditions, including the presence of competitor ions, were investigated. Maximum antimony binding and selectivity was at pH 3.0. Variation in saturation capacity with respect to the crosslinker amount matched with the calculated capacity values. Maximum uptake obtained was 4.6 and 3.2 mmol/g for Sb(III) and Sb(V) respectively. Tartrate salt of Sb(III) showed better binding through the interaction of tartrate with the imidazole moieties of the polymer. In less than 15 min, saturation capacity was achieved for Sb(III), while over 90% of uptake was complete for Sb(V). Investigations on sorption mechanism, which included synthesis and comparative evaluation of the non-ionic counterpart polyvinylimidazole as sorbent, indicated the uptake to be through anion exchange. Sb(III) specific binding against Sb(V) was seen in the presence of nitrilotriacetic acid.

Mechanism study of nitrilotriacetic acid-modified premagnetized Fe0/H2O2 for removing sulfamethazine

Sulfamethazine (SMT) is extensively used as growth promoters and antibacterial drugs. In this study, premagnetized Fe0 was used to catalyze H2O2 decomposition (pre-Fe0/H2O2) in the presence of nitrilotriacetic acid (NTA) to remove SMT at neutral pH conditions. In all, 30.3% and 99.8% of SMT were removed by the pre-Fe0/H2O2 process (60 min) and the pre-Fe0-NTA/H2O2 process (30 min), respectively. The removal rate of SMT in the pre-Fe0-NTA/H2O2 process was 2.5 times larger than that in the Fe0-NTA/H2O2 process. Electron paramagnetic resonance signals indicated that more radicals were generated in the pre-Fe0-NTA/H2O2 system. SMT and NTA and their degradation by-products adsorbed on pre-Fe0 reduced the contact angle of the particle and prevented the formation of Fe3O4 on the particle surface, thus accelerating Fe0 corrosion. Tafel scan images confirmed the enhancement of Fe0 corrosion in the presence of NTA and magnetic field. The Fe0 corrosion rate (109) after 20 min of reaction was 6.61 cm/s in pre-Fe0-NTA/H2O2, much higher than that in Fe0/H2O2 (0.73 cm/s), pre-Fe0/H2O2 (1.47 cm/s) and Fe0-NTA/H2O2 (2.94 cm/s). Pre-Fe0-NTA/H2O2 could also keep the fast SMT removal with eight consecutive runs without the addition of pre-Fe0 and NTA and presented high efficiency for SMT removal in real municipal wastewater.

Nickel spiking to improve the methane yield of sewage sludge

The presence of micro-nutrients can be stimulatory for the anaerobic digestion (AD) of hardly degradable wastes and thus, improve process performance. Among the essential trace elements, nickel is involved in multiple important enzymes necessary for efficient AD. The present study investigates the effect of nickel spiked sewage sludge on batch and continuous mode operation. Metal spiking was conducted in the form of nanoparticles (Ni-NPs) and salt (NiCl2·6H2O). Results from batch assays showed that 5 mgNi-Salt/kgVS in the presence of Nitrilotriacetic acid (NTA) enhanced the methane yield by ∼10% compared to the untreated sample. The impact of Ni-NPs in the AD process was also positive, but slightly lower compared to the effect of NiCl2·6H2O. The stimulatory impact of Ni was also revealed in continuously fed digester boosting the methane yield by ∼8%. Overall, the improved methane production indicated that methanogenic archaea were favoured by the simultaneous supplementation of Ni and NTA.

UV/Nitrilotriacetic Acid Process as a Novel Strategy for Efficient Photoreductive Degradation of Perfluorooctanesulfonate.

Perfluorooctanesulfonate (PFOS) is a toxic, bioaccumulative, and highly persistent anthropogenic chemical. Hydrated electrons ( eaq-) are potent nucleophiles that can effectively decompose PFOS. In previous studies, eaq- are mainly produced by photoionization of aqueous anions or aromatic compounds. In this study, we proposed a new photolytic strategy to generate eaq- and in turn decompose PFOS, which utilizes nitrilotriacetic acid (NTA) as a photosensitizer to induce water photodissociation and photoionization, and subsequently as a scavenger of hydroxyl radical (•OH) to minimize the geminate recombination between •OH and eaq-. The net effect is to increase the amount of eaq- available for PFOS degradation. The UV/NTA process achieved a high PFOS degradation ratio of 85.4% and a defluorination ratio of 46.8% within 10 h. A pseudo-first-order rate constant ( k) of 0.27 h-1 was obtained. The laser flash photolysis study indicates that eaq- is the dominant reactive species responsible for PFOS decomposition. The generation of eaq- is greatly enhanced and its half-life is significantly prolonged in the presence of NTA. The electron spin resonance (ESR) measurement verified the photodissociation of water by detecting •OH. The model compound study indicates that the acetate and amine groups are the primary reactive sites.

TCE degradation in groundwater by chelators-assisted Fenton-like reaction of magnetite: Sand columns demonstration

Trichloroethylene (TCE) degradation in sand columns has been investigated to evaluate the potential of chelates-enhanced Fenton-like reaction with magnetite as iron source for in situ treatment of TCE-contaminated groundwater. The results showed that successful degradation of TCE in sand columns was obtained by nitrilotriacetic acid (NTA)-assisted Fenton-like reaction of magnetite. Addition of ethylenediaminedisuccinic acid (EDDS) resulted in an inhibitory effect on TCE degradation in sand columns. Similar to EDDS, addition of ethylenediaminetetraacetic acid (EDTA) also led to an inhibition of TCE degradation in sand column with small content of magnetite (0.5 w.t.%), but enhanced TCE degradation in sand column with high content of magnetite (7.0 w.t.%). Additionally, the presence of NTA, EDDS and EDTA greatly decreased H2O2 uptake in sand columns due to the competition between chelates and H2O2 for surface sites on magnetite (and sand). Furthermore, the presented results show that magnetite in sand columns remained stable in a long period operation of 230 days without significant loss of performance in terms of TCE degradation and H2O2 uptake. Moreover, it was found that TCE was degraded mainly to formic acid and chloride ion, and the formation of chlorinated organic intermediates was minimal by this process.

Increased accumulation of Pb and Cd from contaminated soil with Scirpus triqueter by the combined application of NTA and APG

Phytoremediation of heavy metals contaminated soils shows many advantages and it can be improved by adding chelating agents and surfactants. In this study, pot culture experiments were set up to explore the effect of alone application of nitrilotriacetic acid (NTA) and combined application of NTA and alkyl polyglucoside (APG) on changes in absorption and adsorption of heavy metals by root of Scirpus triqueter and bioaccumulation of metals in single or co-contamination. Different additives were added into the soils artificially after 10 d and heavy metals extracted from different plant tissues were analyzed after 60 d. Results showed that more cadmium (Cd) was adsorbed on the root surface while more lead (Pb) was absorbed in root interior with the combined application of NTA and APG during phytoremediation of single contaminated soil. In co-contaminated soils, such a combined application not only strengthened the plant growth, but also promoted accumulation of Pb and Cd by Scirpus triqueter. NTA improved absorption amounts of Pb (9.7-fold) and Cd (1.0-fold) in root interior significantly. APG induced more metals to gather on the root surface in the presence of NTA and the adsorption amounts of Pb and Cd ranged from 26.2 and 17.7 mg kg−1 to 412 and 46.0 mg kg−1 respectively. Besides, the coexistence metal increased bioaccumulation of another metal under combined application of NTA and APG in co-contamination of Pb and Cd. In conclusion, the combined application of NTA and APG would be beneficial to accumulate Pb and Cd from contaminated soils by Scirpus triqueter.

Can freshwater phytoplankton access cadmium bound to low‐molecular‐weight thiols?

AbstractRecent studies have suggested that low‐molecular‐weight (LMW) ligands can enhance trace metal uptake by marine diatoms. We have extended this work to freshwater phytoplankton and have investigated Cd bioavailability in the presence of LMW thiols, with two green algae (Chlamydomonas reinhardtii and Pseudokirchneriella subcapitata) and a cyanobacterium (Anabaena flos‐aquae). Using nitrilotriacetic acid (NTA) to hold the free Cd2+ concentration constant, we progressively added cysteine to the exposure medium and determined short‐term Cd uptake rates for each organism; the Cd uptake rates remained constant and were unaffected even when the concentrations of the Cd‐cysteine complexes exceeded that of the free Cd2+. Similar results were obtained with algae pre‐acclimated to different nitrogen sources or low zinc concentrations, even though such treatments affect their ability to utilize amino acids or take up Cd. A lack of effect was also observed for the two green algae with penicillamine, mercaptosuccinic acid, dithiothreitol and glutathione. These results suggest that the Cd‐thiol complexes do not contribute to Cd uptake. However, when the experiments were repeated with cysteine in the absence of NTA, at the same Cd2+ concentration, a significantly higher Cd uptake rate was observed in the presence of the L‐ or D‐cysteine stereoisomers than in the presence of NTA. This enhancement of Cd uptake in the presence of cysteine alone was sensitive to the nitrogen nutrition of these microorganisms, and we suggest that the enhancement likely results from biologically‐induced chemical oxidation of cysteine in the boundary layer adjacent to the algal cell.

Enhanced heterogeneous and homogeneous Fenton-like degradation of carbamazepine by nano-Fe3O4/H2O2 with nitrilotriacetic acid

The influence of a biodegradable agent, nitrilotriacetic acid (NTA), on the degradation of the model compound carbamazepine (CBZ) by the nano-Fe3O4/H2O2 system was investigated. The results showed that the presence of NTA can provide better performance of the nano-Fe3O4/H2O2 system for CBZ degradation at reduced usage of H2O2 and nano-Fe3O4. The optimal concentration of NTA was determined to be 0.5–1.0mM. The first-order rate constant, kapp, for CBZ degradation by 1.0gL−1 of nano-Fe3O4 and 100mM of H2O2 in the presence of 0.5mM of NTA at an initial neutral pH was determined to be 4.32×10−2min−1, which was 80 times larger than that in the absence of NTA. In addition, the kapp value increased with the increase in nano-Fe3O4 concentration from 0.1 to 3.0gL−1, and the H2O2 concentration increased from 5 to 600mM. The initial pH of CBZ solutions over a range of pH 5.0–9.0 did not affect the kapp value of CBZ (p=0.08). A decrease in the initial concentration of CBZ from 6.35×10−2 to 1.06×10−2 mM resulted in an increase of the kapp value from 4.32×10−2 to 1.51×10−1min−1. Moreover, the results indicated that the degradation intermediates were generated by the attack of OH. The degradation mechanism of CBZ included both an enhanced heterogeneous Fenton-like reaction on the Fe3O4 nanoparticle surface and an enhanced homogeneous Fenton-like reaction in the aqueous phase by Fe-NTA complexes.

Complex formation of MnII with tetra(p-tert-butyl)thiacalix[4]arene acid in aqueous solutions of surfactants and polymers

The formation of manganese(II) complexes with different stereoisomers of tetraacid based on p-tert-butylthiacalix[4]arene in water, in micellar solutions of nonionogenic surfactants, and in polymer solutions was studied. The formation of complexes with different degrees of ligand protonation was revealed by pH-metric titration and nuclear magnetic relaxation. On the basis of experimental data, the composition and stability constants of the solubilized complexes of stereoisomers of thiacalixarene acid with manganese(II) ions were determined using mathematical simulation methods. The manganese thiacalixarene complexes are unstable in solutions, especially upon the addition of calcium cations and in the presence of nitrilotriacetic acid.

Sorption behaviour of Co(II) and Cu(II) on chitosan in presence of nitrilotriacetic acid

Separation and isolation of radioactive cobalt ( 60Co), one of the main contributors towards the activity build up in nuclear reactors, is essential for radioactive waste volume reduction during nuclear reactor decontamination procedures. In this context, sorption of free and complexed Co(II), Cu(II) and nitrilotriacetic acid (NTA) on the biosorbent, chitosan was studied. A detailed investigation on the role of pH on sorption of Co(II), Cu(II) and NTA was done. Uptake capacities of the metal ions and NTA were measured within pH range of 2.0–7.0. At pH above 5, the NTA uptake capacities were found to be higher in presence of the metal ions than in their absence. Effect of NTA was found to be more pronounced on copper uptake than on cobalt uptake. Significant change in selectivity of chitosan towards metal ion uptake from NTA medium was observed with respect to change in pH. At pH 2.9, the uptake of cobalt was found to be more than that of copper, while the selectivity was reversed at pH 6.0. The respective selectivity coefficient ( k Co/Cu) values were found to be 2.06 and 0.072.

Redox behavior of Ce(IV)/Ce(III) in the presence of nitrilotriacetic acid: A surrogate study for An(IV)/An(III) redox behavior

AbstractUsing cyclic voltammetry, we investigated the redox behavior of Ce(IV)/Ce(III), which is a surrogate for An(IV)/An(III) (An=actinides), in a solution of nitrilotriacetic acid (NTA) at 25 °C. The cyclic voltammogram of Ce in a 0.1 M NTA solution at pH 6 showed a reversible one-electron redox reaction for Ce(IV)/Ce(III) at 0.51 Vvs.Ag/AgCl. This redox potential was much lower than that obtained in 1 M nitric acid, indicating that Ce(IV) was preferentially stabilized by complexation with NTA. The redox potential in the NTA solution was independent of the Ce concentration from 2 to 20 mM, NTA concentration from 5 to 200 mM and pH between 3 and 7. These results indicated that no polymerization and no additional coordination of NTA and OH−to the Ce(III)-NTA complex took place during the redox reaction. As the speciation calculation of Ce(III) in the NTA solution showed that the predominant species was CeIII(nta)23−(H3nta=NTA), the redox reaction of the Ce-NTA complex was expressed by the following: CeIV(nta)22−+e−⇋CeIII(nta)23−. The logarithm of the stability constant of CeIV(nta)22−was calculated to be 38.6±0.8 forI=0 from the redox potential shift of Ce(IV)/Ce(III) in the NTA solution. The value was in good accordance with the stability constant of the NpIV(nta)22−complex, demonstrating that the aqueous coordination chemistry of Ce(IV) with NTA is quite similar to that of An(IV). These results strongly suggest that a negative shift of the Pu(IV)/Pu(III) redox potential in the NTA solution should make Pu(IV) more stable than Pu(III) even in a reducing environment.

Photochemical synthesis of CdSe and PbSe nanowire arrays on a porous aluminum oxide template

CdSe and PbSe nanowire arrays have been successfully prepared by a photochemical method in porous anodic aluminum oxide template from an aqueous solution of lead acetate, cadmium chloride and sodium selenosulfate in the presence of nitrilotriacetic acid. The products were characterized by XRD, TEM, SEM, PL and UV–vis.