Control of Fe3+ coordination by excess Cl− in alcohol solutions

We spectroscopically investigated coordination state of Fe³⁺ in methanol (MeOH) and ethanol (EtOH) solutions against Cl⁻ concentration ([Cl⁻]). In both the system, we observed characteristic absorption bands due to the FeCl₄ complex at high-[Cl⁻] region. In the MeOH system, the proportion (r) of [FeCl₄]⁻ exhibits a stationary value of 0.2–0.3 in the intermediate region of 10 mM < [Cl⁻] < 50 mM, which is interpretted in terms of [FeCl_nL_6−n]³⁻ⁿ (n = 1 and 2). In the EtOH system, r steeply increases from 0.1 at [Cl⁻] = 1.5 mM to 0.7 at [Cl⁻] = 3.5 mM, indicating direct transformation from [FeL₆]³⁺ to [FeCl₄]⁻. We further found that the coordination change significantly decreases the redox potential of Fe²⁺/Fe³⁺.

Fe³⁺ coordination in alcohol solution can be controlled by the Cl⁻ concentration ([Cl⁻]). The coordination state changes from FeL₆ (L: solvent molecule) to FeCl₄ type via FeCl_nL_6−n with increases in [Cl⁻].     

Influence of Cl− ions on anodic polarization behaviour of API X80 steel in high potential/current density conditions in Na2SO4 solution

Pipeline steel has considerable risk of corrosion in the high voltage direct current interference cases. Thus, under high potential/current density conditions, the anodic polarization behaviour of X80 steel in Na₂SO₄ solution and the influence of Cl⁻ ions were investigated using reversed potentiodynamic polarization, the current interrupt method, galvanostatic polarization, scanning electron microscopy, and X-ray photoelectron spectroscopy. In the Na₂SO₄ solution free of Cl⁻ ions, steel was passivated above 0.120 A cm⁻² and the potential increased from −0.32 V to 1.43 V. The passive film was composed of Fe₃O₄, γ-Fe₂O₃, and FeOOH. The addition of Cl⁻ ions observably influenced the passivation by attacking the passivate film. Low concentration of Cl⁻ ions (<5 mg L⁻¹ NaCl) could set higher demands of current density to achieve passivation and increase the requirement of potential to maintain passivation. A high concentration of Cl⁻ ions (>5 mg L⁻¹ NaCl) completely prevented passivation, showing strong corrosiveness. Thus, the X80 steel was corroded even under high-current-density conditions. The corrosion products were mainly composed of Fe₃O₄, α-Fe₂O₃, and FeOOH.

X80 steel gets passivated in high potential/current density conditions in Na₂SO₄ solution. Low concentration of Cl⁻ ions weakens the passivation. High concentration of Cl⁻ ions totally prevents the passivation.     

The rapid microwave-assisted hydrothermal synthesis of NASICON-structured Na3V2O2x(PO4)2F3−2x (0 < x ≤ 1) cathode materials for Na-ion batteries

NASICON-structured Na₃V₂O_2x(PO₄)₂F_3−2x (0 < x ≤ 1) solid solutions have been prepared using a microwave-assisted hydrothermal (MW-HT) technique. Well-crystallized phases were obtained for x = 1 and 0.4 by reacting V₂O₅, NH₄H₂PO₄, and NaF precursors at temperatures as low as 180–200 °C for less than 15 min. Various available and inexpensive reducing agents were used to control the vanadium oxidation state and final product morphology. The vanadium oxidation state and O/F ratios were assessed using electron energy loss spectroscopy and infrared spectroscopy. According to electron diffraction and powder X-ray diffraction, the Na₃V₂O_2x(PO₄)₂F_3−2x solid solutions crystallized in a metastable disordered I4/mmm structure (a = 6.38643(4) Å, c = 10.62375(8) Å for Na₃V₂O₂(PO₄)₂F and a = 6.39455(5) Å, c = 10.6988(2) Å for Na₃V₂O_0.8(PO₄)₂F_2.2). With respect to electrochemical Na⁺ (de)insertion as positive electrodes (cathodes) for Na-ion batteries, the as-synthesized materials displayed two sloping plateaus upon charge and discharge, centered near 3.5–3.6 V and 4.0–4.1 V vs. Na⁺/Na, respectively, with a reversible capacity of ∼110 mA h g⁻¹. The application of a conducting carbon coating through the surface polymerization of dopamine with subsequent annealing at 500 °C improved both the rate capability (∼55 mA h g⁻¹ at a discharge rate of 10C) and capacity retention (∼93% after 50 cycles at a discharge rate of C/2).

NASICON-structured Na₃V₂O_2x(PO₄)₂F_3−2x (0 < x ≤ 1) solid solutions have been prepared using a microwave-assisted hydrothermal (MW-HT) technique.     

Structure and transport properties of triple-conducting BaxSr1−xTi1−yFeyO3−δ oxides

In this work, Ba_xSr_1−xTi_1−yFe_yO_3−δ perovskite-based mixed conducting ceramics (for x = 0, 0.2, 0.5 and y = 0.1, 0.8) were synthesized and studied. The structural analysis based on the X-ray diffraction results showed significant changes in the unit cell volume and Fe(Ti)–O distance as a function of Ba content. The morphology of the synthesized samples studied by means of scanning electron microscopy has shown different microstructures for different contents of barium and iron. Electrochemical impedance spectroscopy studies of transport properties in a wide temperature range in the dry- and wet air confirmed the influence of barium cations on charge transport in the studied samples. The total conductivity values were in the range of 10⁻³ to 10⁰ S cm⁻¹ at 600 °C. Depending on the barium and iron content, the observed change of conductivity either increases or decreases in humidified air. Thermogravimetric measurements have shown the existence of proton defects in some of the analysed materials. The highest observed molar proton concentration, equal to 5.0 × 10⁻² mol mol⁻¹ at 300 °C, was obtained for Ba_0.2Sr_0.8Ti_0.9Fe_0.1O_2.95. The relations between the structure, morphology and electrical conductivity were discussed.

Ba_xSr_1−xTi_1−yFe_yO_3−δ-based perovskite materials with different barium and iron contents are reported as triple conducting oxides (TCOs), which may conduct three charge carriers: oxygen ions, protons and electrons/holes.     

Zinc(ii)-based coordination polymer encapsulated Tb3+ as a multi-responsive luminescent sensor for Ru3+, Fe3+, CrO42−, Cr2O72− and MnO4−

A zinc(ii)-based coordination polymer (CP), namely [Zn(modbc)₂]_n (Zn-CP) (modbc = 2-methyl-6-oxygen-1,6-dihydro-3,4′-bipyridine-5-carbonitrile), has been synthesized and characterized. Single-crystal structural determination reveals that Zn-CP is a two-dimensional framework structure with tetranuclear homometallic Zn₄(modbc)₄ units cross-linked by modbc. The excellent luminescence as well as good stability of Zn-CP do not enable it to have selective sensing capability for different ions. After encapsulation of Tb³⁺ in Zn-CP, the as-obtained fluorescent functionalized Tb³⁺@Zn-CP maintained excellent luminescence as well as stability, which made it a highly selective and sensitive multiresponsive luminescent sensor for Ru³⁺, Fe³⁺, CrO₄²⁻, Cr₂O₇²⁻, and MnO₄⁻ with high sensitivity, good anti-interference performance, and quick response time (∼10 s). The detection limits are 0.27 μM, 0.57 μM, 0.10 μM, 0.43 μM and 0.15 μM, respectively. A possible sensing mechanism was discussed in detail.

A composite, Tb³⁺@Zn-CP, for sensing Ru³⁺, Fe³⁺, CrO₄²⁻, Cr₂O₇²⁻ and MnO₄⁻ with fast response times was reported.     

Synthesis of Fe3O4@PVBC–TMT nanoparticles for the efficient removal of heavy metals ions

Core–shell magnetic Fe₃O₄@PVBC–TMT (Fe₃O₄@polyvinylbenzyl chloride–trithiocyanuric acid) nanoparticles containing trithiocyanuric acid groups were fabricated and employed for the fast removal of heavy metals from an aquatic environment. The morphology, structure and properties of Fe₃O₄@PVBC–TMT nanoparticles were characterized by a series of modern analytical tools. The adsorption behavior of the Fe₃O₄@PVBC–TMT nanoparticles for heavy metals ions in aqueous solutions was investigated by batch experiments. The maximum removal capacities of the Fe₃O₄@PVBC–TMT nanoparticles toward Mn²⁺, Ni²⁺, Cu²⁺, Cd²⁺ and Pb²⁺ ions were 127.4, 146.6, 180.5, 311.5, and 528.8 mg g⁻¹, respectively. Importantly, it is found that Pb²⁺ ions can be completely and quickly removed by the Fe₃O₄@PVBC–TMT nanoparticles. The equilibrium was established within 6 min, and the removal efficiencies were found to be 99.9%, 99.8% and 99.5% for Pb²⁺ ions at the initial concentrations of 100 mg L⁻¹, 200 mg L⁻¹ and 300 mg L⁻¹, respectively. It is hoped that the core–shell magnetic Fe₃O₄@PVBC–TMT nanoparticles may find application in wastewater treatment.

Core–shell Fe₃O₄@PVBC–TMT nanoparticles were fabricated and served as a valid magnetic adsorbent for the removal of heavy metals ions.     

Atmosphere-sensitive photoluminescence of CoxFe3−xO4 metal oxide nanoparticles

In this work the photoluminescence (PL) of Co_xFe_3−xO₄ spinel oxide nanoparticles under pulsed UV laser irradiation (λ_exc = 270 nm) is investigated for varying Co/Fe ratios (x = 0.4_⋯2.5). A broad emission in the green spectral range is observed, exhibiting two maxima at around 506 nm, which is dominant for Fe-rich nanoparticles (x = 0.4, 0.9), and at around 530 nm, that is more pronounced for Co-rich nanoparticles (x > 1.6). As examinations in different atmospheres show that the observed emission reacts sensitively to the presence of water, it is proposed that the emission is mainly caused by OH groups with terminal or bridging metal–O bonds on the Co_xFe_3−xO₄ surface. Raman spectroscopy supports that the emission maximum at 506 nm corresponds to terminal OH groups bound to metal cations on tetrahedral sites (i.e., Fe³⁺), while the maximum around 530 nm corresponds to terminal OH groups bound to metal cations on octahedral sites (i.e., Co³⁺). Photoinduced dehydroxylation shows that OH groups can be removed on Fe-rich nanoparticles more easily, leading to a conversion process and the formation of new OH groups with different bonds to the surface. As such behavior is not observed for Co_xFe_3−xO₄ with x > 1.6, we conclude that the OH groups are more stable against dehydroxylation on Co-rich nanoparticles. The higher OH stability is expected to lead to a higher catalytic activity of Co-rich cobalt ferrites in the electrochemical generation of oxygen.

Co_xFe_3−xO₄ (0.4 < x < 2.5) nanoparticles show a broad green emission induced by surface OH-groups with a lower stability regarding UV-photoinduced dehydroxylation on Fe-rich (x ≤ 1.6) nanoparticles.     

Solid base catalysts derived from Ca–Al–X (X = F−, Cl− and Br−) layered double hydroxides for methanolysis of propylene carbonate

The Ca–Al and Ca–Al–X (X = F⁻, Cl⁻ and Br⁻) catalysts were prepared via thermal decomposition of Ca–Al layered double hydroxides (LDHs), and tested for methanolysis of propylene carbonate (PC) to produce dimethyl carbonate (DMC). The catalytic performance of these catalysts increased in the order of Ca–Al–Br⁻ < Ca–Al < Ca–Al–Cl⁻ < Ca–Al–F⁻, which was consistent with the strong basicity of these materials. The recyclability test results showed that the addition of Al and halogens (F⁻, Cl⁻ and Br⁻) not only stabilized the CaO but also improved the recyclability of the catalysts. Particularly, the Ca–Al–F⁻ catalyst exerted the highest stability after 10 recycles. These catalysts have an important value for the exploitation of DMC synthesis by transesterification of PC with methanol.

The CA-F⁻ catalyst modified with Al³⁺ and F⁻ was highly active and recyclable for dimethyl carbonate synthesis.     

Solventless synthesis of nanospinel Ni1−xCoxFe2O4 (0 ≤ x ≤ 1) solid solutions for efficient electrochemical water splitting and supercapacitance

The formation of solid solutions represents a robust strategy for modulating the electronic properties and improving the electrochemical performance of spinel ferrites. However, solid solutions have been predominantly prepared via wet chemical routes, which involve the use of harmful and/or expensive chemicals. In the present study, a facile, inexpensive and environmentally benign solventless route is employed for the composition-controlled synthesis of nanoscopic Ni_1−xCo_xFe₂O₄ (0 ≤ x ≤ 1) solid solutions. The physicochemical characterization of the samples was performed by p-XRD, SEM, EDX, XPS, TEM, HRTEM and UV-Vis techniques. A systematic investigation was also carried out to elucidate the electrochemical performance of the prepared nanospinels towards energy generation and storage. Based on the results of CV, GCD, and stability tests, the Ni_0.4Co_0.6Fe₂O₄ electrode showed the highest performance for the supercapacitor electrode exhibiting a specific capacitance of 237 F g⁻¹, superior energy density of 10.3 W h kg⁻¹ and a high power density with a peak value of 4208 W kg⁻¹, and 100% of its charge storage capacity was retained after 4000 cycles with 97% coulombic efficiency. For HER, the Ni_0.6Co_0.4Fe₂O₄ and CoFe₂O₄ electrodes showed low overpotentials of 168 and 169 mV, respectively, indicating better catalytic activity. For OER, the Ni_0.8Co_0.2Fe₂O₄ electrode exhibited a lower overpotential of 320 mV at a current density of 10 mA cm⁻², with a Tafel slope of 79 mV dec⁻¹, demonstrating a fast and efficient process. These results indicated that nanospinel ferrite solid solutions could be employed as promising electrode materials for supercapacitor and water splitting applications.

The formation of solid solutions represents a robust strategy for modulating the electronic properties and improving the electrochemical performance of spinel ferrites.     

A series of Ln4III clusters: Dy4 single molecule magnet and Tb4 multi-responsive luminescent sensor for Fe3+, CrO42−/Cr2O72− and 4-nitroaniline

Five tetranuclear lanthanide clusters of compositions [Ln₄L₄(NO₃)₂(Piv)₂]·2CH₃OH (Ln = Gd (1), Tb (2), Dy (3), Ho (4), Er (5); H₂L = 2-(((2-hydroxy-3-methoxybenzyl)imino)methyl)-6-methoxyphenol; Piv = pivalic acid) were synthesized under solvothermal conditions. The structures of 1–5 were characterized by single-crystal X-ray crystallography. Complexes 1–5 possess a zig-zag topology with [Ln₄O₆] cores being formed by the fusion of oxygen atom-bridged two [Ln₂O₂] moieties. Direct-current magnetic susceptibility studied in the 2–300 K range revealed weak antiferromagnetic interactions in 1, 2, 4, 5 and ferromagnetic interactions in 3. Complex 3 exhibits single molecule magnet (SMM) behavior. The luminescence studies indicated that complex 2 can serve as highly sensitive and selective luminescent materials for Fe³⁺, CrO₄²⁻, Cr₂O₇²⁻ and 4-nitroaniline (4-NA), demonstrating that complex 2 should be a potential candidate for multi-responsive luminescent sensor.

Five tetranuclear lanthanide clusters were synthesized. Dy₄ complex exhibits single molecule magnet (SMM) behavior and Tb₄ compound shows sensing properties towards Fe³⁺, CrO₄²⁻, Cr₂O₇²⁻ and 4-nitroaniline (4-NA).     

Efficient activation of persulfate by Fe3O4@β-cyclodextrin nanocomposite for removal of bisphenol A

Experimental studies were conducted to investigate the degradation of bisphenol A (BPA) by using persulfate (PS) as the oxidant and Fe₃O₄@β-cyclodextrin (β-CD) nanocomposite as a heterogeneous activator. The catalytic activity was evaluated in consideration of the effect of various parameters, such as pH value, PS concentration and Fe₃O₄@β-CD load. The results showed that 100% removal of BPA was gained at pH 3.0 with 5 mM PS, 1.0 g L⁻¹ Fe₃O₄@β-CD, and 0.1 mM BPA in 120 min. Further, the catalytic activity of Fe₃O₄@β-CD nanocomposite was observed as much higher when compared with Fe₃O₄ nanoparticles alone. The sulfate and hydroxyl radicals referred to in the Fe₃O₄@β-CD/PS system were determined as the reactive species responsible for the degradation of BPA by radical quenching and electron spin resonance (ESR) tests. In addition, the catalyst also possessed with accepted reusability and stability. On the basis of the results of the effect of chloride ions (Cl⁻), β-CD was found to play a crucial role in reducing interference from Cl⁻ ions, and lead to achieve higher removal efficiency for BPA in Fe₃O₄@β-CD/PS system. A possible mechanistic process of BPA degradation was proposed according to the identified intermediates by gas chromatography-mass spectroscopy (GC-MS).

Persulfate (PS), the most commonly used activator for in situ chemical oxidation (ISCO), could couple with Fe₃O₄@β-CD for effectively degrading BPA.     

Adsorption of ng L−1-level arsenic by ZIF-8 nanoparticles: application to the monitoring of environmental water

The provisional contamination level of arsenic in drinking water is 10 μg L⁻¹. For decreasing this value to a safer level, a more precise method for analyzing dissolved arsenic is required. With this aim, we synthesized zeolitic imidazolate framework-8 (ZIF-8) in the aqueous phase and characterized its potential application for monitoring the trace arsenic in fresh water. In this regard, we report following three notable outcomes. First, we demonstrate the excellent performance of ZIF-8 nanoparticles (nZIF-8) for the adsorption of ng L⁻¹ levels of AsO₄³⁻. nZIF-8 is able to adsorb over 99% of arsenic from as low as 10 ng L⁻¹ AsO₄³⁻ solutions. This performance was maintained even in the presence of commonly coexisting anions, for example, >90% adsorption from a 0.1 μg L⁻¹ arsenic solution was observed in the presence of 10 mg L⁻¹ of Cl⁻, NO₃⁻, CO₃²⁻, or SO₄²⁻, or 1 mg L⁻¹ of PO₄³⁻. Second, we clarified that the mechanism of arsenic adsorption by ZIF-8 is simply a ligand exchange process, in which the As(v) oxide anion replaces the imidazolate unit in the framework. Third, we propose a handy scheme for the analysis of ng L⁻¹ levels of arsenic in drinking water, in which nZIF-8 is used for the concentration of trace level AsO₄³⁻. By doing this, as low as 100 ng L⁻¹ arsenate in drinking water can be quantified by colorimetric analysis, the detection limit of which is 5 μg L⁻¹ in pure water. The application of this scheme is expected to highly enhance AsO₄³⁻ detection first by concentrating it to an easily detectable range, and second by excluding the majority of interfering ions present in the system. Therefore, a reduction in the minimum quantifying limit of arsenic in fresh water to as low as 1 ng L⁻¹ can be expected if the method is coupled with ICP-MS.

ZIF-8 nanoparticles highly selectively uptakes ultra-trace concentration arsenate. The material can be used for high precision monitoring of the ion when coupled with handy analytical tools.     

Evaluation of BaCo0.4Fe0.4Zr0.2−xNixO3−δ perovskite cathode using nickel as a sintering aid for IT-SOFC

In this research work, BaCo₀.₄Fe₀.₄Zr_0.2−xNi_xO_3−δ (x = 0, 0.01, 0.02, 0.03, 0.04) perovskite cathode material for IT-SOFC is synthesized successfully using a combustion method and sintered at low temperature. The effects of nickel as a sintering aid on the properties of BaCo₀.₄Fe₀.₄Zr₀.₂O_3−δ are investigated through different characterization methods. The addition of nickel increased the densification and grain growth at a lower sintering temperature 1200 °C. XRD analysis confirms a single phase of BaCo₀.₄Fe₀.₄Zr₀.₂O_3−δ, and an increase in crystalline size is observed. SEM micrographs show formation of dense microstructure with increased nickel concentration. TGA analysis revealed that BaCo₀.₄Fe₀.₄Zr_0.2−xNi_x cathode materials are thermally stable within the SOFC temperature range, and negligible weight loss of 2.3% is observed. The bonds of hydroxyl groups and metal oxides are confirmed for all samples through FTIR analysis. The highest electrical properties are observed for BaCo₀.₄Fe₀.₄Zr_0.2−xNi_x (x = 0.04) due to increased densification and electronic defects compared to other compositions. The maximum power density of 0.47 W cm⁻² is obtained for a cell having cathode material BaCo₀.₄Fe₀.₄Zr_0.2−xNi_x (x = 0.02) owing to its permeable and well-connected structure compared to others.

Electrochemical performance of BaCo₀.₄Fe₀.₄Zr_0.2−xNi_xO_3−δ at 600 °C.     

A luminescent Cd(ii) coordination polymer as a multi-responsive fluorescent sensor for Zn2+, Fe3+ and Cr2O72− in water with fluorescence enhancement or quenching

A luminescent Cd(ii) coordination polymer, namely {[Cd(btic)(phen)]·0.5H₂O}_n (CP-1) (H₂btic = 5-(2-benzothiazolyl)isophthalic acid, phen = 1,10-phenanthroline), was constructed through the mixed-ligand method under solvothermal conditions. CP-1 manifests a chain structure decorated with uncoordinated Lewis basic N and S donors. CP-1 exhibits high sensing towards Zn²⁺, Fe³⁺ and Cr₂O₇²⁻ ions with fluorescence enhancement or quenching. CP-1 exhibited a fluorescence enhancement for Zn²⁺ ions through weak binding to S and N atoms, and a fluorescence quenching for Fe³⁺ and Cr₂O₇²⁻ ions by an energy transfer process. The binding constants were calculated as 1.812 × 10⁴ mol⁻¹ for Zn²⁺, 4.959 × 10⁴ mol⁻¹ for Fe³⁺ and 1.793 × 10⁴ mol⁻¹ for Cr₂O₇²⁻. This study shows CP-1 as a rare multi-responsive sensor material for the efficient detection of Zn²⁺, Fe³⁺ and Cr₂O₇²⁻ ions.

A luminescent Cd(ii) coordination polymer can act as a multi-responsive sensor for efficiently detecting Zn²⁺, Fe³⁺ and Cr₂O₇²⁻ ions.     

Facile preparation of amidoxime-functionalized Fe3O4@SiO2-g-PAMAM-AO magnetic composites for enhanced adsorption of Pb(ii) and Ni(ii) from aqueous solution

In this paper, using amidoxime as a functional monomer, different generations of polyamidoxime dendrimer magnetic microspheres (Fe₃O₄@SiO₂-g-PAMAM-AO) were fabricated to adsorb Pb²⁺ and Ni²⁺ in aqueous solution. The magnetic adsorbents were characterized by FTIR, XRD, SEM, XPS, TEM, EDS, TGA and BET. The effects of different factors (such as solution pH, adsorption time, adsorption temperature, adsorbent dosage etc.) on adsorption were evaluated. Fe₃O₄@SiO₂-g-PAMAM-AO has a maximum Pb(ii) adsorption of 157.25 mg g⁻¹ (100 mg L⁻¹) at pH 5.5. Furthermore, Fe₃O₄@SiO₂-g-PAMAM-AO showed an excellent adsorption performance for the removal of Ni(ii) with a maximum adsorption capacity of 191.78 mg g⁻¹ (100 mg L⁻¹) at pH 8.0. The sorption isotherm data fitted the Freundlich isotherm model well. Adsorption kinetics analysis showed that it was best described by the pseudo-second-order rate model. Desorption experiment results showed that the adsorbent can be reused in the adsorption–desorption cycles.

In this paper, using amidoxime as a functional monomer, different generations of polyamidoxime dendrimer magnetic microspheres (Fe₃O₄@SiO₂-g-PAMAM-AO) were fabricated to adsorb Pb²⁺ and Ni²⁺ in aqueous solution.     

Weak magnetic field enhances the activation of peroxymonosulfate by ZnO@Fe3O4

The effect of weak magnetic field (WMF) on Acid Orange 7 (AO7) removal by ZnO@Fe₃O₄/peroxymonosulphate (PMS) was investigated. The results showed that the AO7 sequestration rate enhanced progressively to 0.14183 min⁻¹ in the presence of WMF, approximately 3 times the 0.04966 min⁻¹ in the absence of WMF. SO₄˙⁻/SO₅˙⁻ and O₂˙⁻ radicals were generated from the decomposition of PMS catalyzed by ZnO@Fe₃O₄ causing the degradation of AO7. In addition, a weak magnetic field promoted the production of O₂˙⁻ radicals and transition of Fe³⁺ to Fe²⁺. Radical-pair theory was used in this study to describe the role of WMF and a possible reaction mechanism was derived. Based on that, the influence of magnetic field flux intensity, pH and the reusability of ZnO@Fe₃O₄ were investigated in this paper.

The effect of weak magnetic field (WFM) on Acid Orange 7 (AO7) removal by ZnO@Fe₃O₄/peroxymonosulphate (PMS) was investigated. And a possible reaction mechanism was derived.     

Recovery of NH4+–N and PO43−–P from urine using sludge-derived biochar as a fertilizer: performance and mechanism

Sludge-derived biochar (BS) was prepared by pyrolyzing municipal sludge at different temperatures and was used to recover NH₄⁺–N and PO₄³⁻–P from urine. The effects of dosage, adsorption time, and urine concentration on the adsorption of NH₄⁺–N and PO₄³⁻–P were investigated, and the adsorbed BS was used as a fertilizer to study its effect on the growth of pakchoi cabbage. The Elovich model was more consistent with the adsorption processes of NH₄⁺–N and PO₄³⁻–P. Both the NH₄⁺–N and PO₄³⁻–P adsorption isotherm model agreed with the Redlich–Peterson model. The Langmuir model showed that the largest adsorption capacity of BS600 for NH₄⁺–N and PO₄³⁻–P could reach 114.64 mg g⁻¹ and 31.05 mg g⁻¹, respectively. The NH₄⁺–N adsorption mechanism of BS may have complexation with O-containing functional groups and precipitation reactions, while the removal mechanism of PO₄³⁻–P was co-precipitation. The pot experiment demonstrated that adsorbed BS600 can better promote the growth of pakchoi cabbage with the same amount of addition. With the addition of 5% adsorbed BS600, the weight of cabbage was 64.49 g heavier than without the addition of BS600. This research provided theoretical support for the recovery of NH₄⁺–N and PO₄³⁻–P from urine as a fertilizer.

Sludge-derived biochar (BS) was prepared by pyrolyzing municipal sludge at different temperatures and was used to recover NH₄⁺–N and PO₄³⁻–P from urine.     

Metal-bio functionalized bismuthmagnetite [Fe3−xBixO4/SiO2@l-ArgEt3+I−/Zn(ii)]: a novel bionanocomposite for the synthesis of 1,2,4,5-tetrahydro-2,4-dioxobenzo[b][1,4]diazepine malononitriles and malonamides at room temperature and under sonication

In this work, a new magnetized composite of bismuth (Fe_3−xBi_xO₄) was prepared and functionalized stepwise with silica, triethylargininium iodide ionic liquid, and Zn(ii) to prepare a multi-layered core–shell bio-nanostructure, [Fe_3−xBi_xO₄/SiO₂@l-ArgEt₃⁺I⁻/Zn(ii)]. The modified bismuth magnetic amino acid-containing nanocomposite was characterized using several techniques including Fourier-transform infrared (FT-IR), X-ray fluorescence (XRF), vibrating sample magnetometer (VSM), field-emission scanning electron microscopy (FESEM), energy dispersive X-ray analysis (EDAX), thermogravimetric/differential scanning calorimetric (TGA/DSC) analysis, X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), and inductively coupled plasma-optical emission spectrometry (ICP-OES). The magnetized bionanocomposite exhibited high catalytic activity for the synthesis of 1,2,4,5-tetrahydro-2,4-dioxobenzo[b][1,4]diazepine malononitriles via five-component reactions between 1,2-phenylenediamines, Meldrum''s acid, malononitrile, aldehydes, and isocyanides at room temperature in ethanol. The efficacy of this protocol was also examined to obtain malonamide derivatives via pseudo six-component reactions of 1,4-phenylenediamine, Meldrum''s acid, malononitrile, aldehydes, and isocyanides. When the above-mentioned MCRs were repeated under the same conditions with the application of sonication, a notable decrease in the reaction time was observed. The recovery and reusability of the metal-bio functionalized bismuthmagnetite were examined successfully in 3 runs. Furthermore, the characteristics of the recovered Fe_3−xBi_xO₄/SiO₂@l-ArgEt₃⁺I⁻/Zn(ii) were investigated though FESEM and EDAX analysis.

In this work, a new magnetized composite of bismuth (Fe_3−xBi_xO₄) was prepared and functionalized stepwise with silica, triethylargininium iodide ionic liquid, and Zn(ii) to prepare a multi-layered core–shell bio-nanostructure, [Fe_3−xBi_xO₄/SiO₂@l-ArgEt₃⁺I⁻/Zn(ii)].     

The cation–anion co-exchange in CsPb1−xFex(Br1−yCly)3 nanocrystals prepared using a hot injection method

All inorganic perovskite nanocrystals (NCs) have wide practical applications for their remarkable optoelectronic properties. To obtain blue-emitting perovskites with high photoluminescence quantum yield and room-temperature ferromagnetism, CsPb_1−xFe_x(Br_1−yCl_y)₃ NCs were synthesized using a hot injection method. The effects of the cation–anion co-exchange on the structural, luminescent and magnetic properties of CsPbBr₃ NCs were studied by X-ray diffraction spectroscopy, photoluminescence spectroscopy, transmission electron microscopy, field emission scanning electron microscopy, and vibrating sample magnetometer. The results indicated that there was cation–anion co-exchange in CsPb_1−xFe_x(Br_1−yCl_y)₃ NCs, while the band-edge energies and PLQY were mainly affected by the anion exchange. The ferromagnetism of CsPb_1−xFe_x(Br_1−yCl_y)₃ NCs had been observed at room temperature, and there was an increase in saturation magnetization with increasing Fe concentration.

All inorganic perovskite nanocrystals (NCs) have wide practical applications for their remarkable optoelectronic properties.     

MoS42− intercalated NiFeTi LDH as an efficient and selective adsorbent for elimination of heavy metals

The enormous increase of heavy metal pollution has led to a rise in demand for synthesizing efficient and stable adsorbents for its treatment. Therefore, we have designed a novel adsorbent by introducing (MoS₄)²⁻ moieties within the layers of NiFeTi LDH-NO₃, via an ion exchange mechanism, as a stable and efficient adsorbent to deal with the increasing water pollution due to heavy metals. Characterization techniques such as XRD, FTIR, TGA, SEM, TEM, and Raman spectroscopy were used to confirm the formation of (MoS₄)²⁻ intercalated NiFeTi LDH and structural changes after the adsorption process. The efficiency of the material was tested with six heavy metal ions, among which it was found to be effective for toxic Pb²⁺ and Ag⁺ ions. When selectivity was studied with all six of the metal ions copresent in one solution, the material showed greater selectivity for Pb²⁺ and Ag⁺ ions with the selectivity order of Ni²⁺ < Cu²⁺ < Zn²⁺ < Fe³⁺ < Pb²⁺ < Ag⁺, with great adsorption capacities of 653 mg g⁻¹ for Pb²⁺ and 856 mg g⁻¹ for Ag⁺ metal ions. Further, the kinetics adsorption study for both the metal ions had a great correlation with the pseudo-second-order model and supported the chemisorption process via the formation of M–S bonding. The adsorption process obeyed the Langmuir model. Therefore, the MoS₄-LDH material could be a promising adsorbent for the removal of heavy metals.

Elimination of the heavy metals by using the MoS₄-LDH adsorbent.