Intermediate Iron Research Articles

Effect of location on green steel production using Australian resources

Hydrogen is being increasingly considered as a chemical feedstock and energy storage vector within the iron and steel industry. This study compares the cost and CO2 emissions associated with green steel production as a function of location for the components in its supply chain between Australia (Pilbara) and China (Beijing). Results are benchmarked against a new facility using conventional coal-based technology, producing Hot Rolled Coil (HRC) steel in China as a common final product. Green steel production in Australia using hydrogen is considerably cheaper and presents lower emissions than exporting the hydrogen and iron ore to China for subsequent processing. Costs are comparable when intermediate Hot Briquetted Iron (HBI) is exported but with increased emissions. However, utilising blue hydrogen produced in China is the most immediately dispatchable with a 35% reduction in CO2 emissions and an increase in levelised cost of steel (LCOS) of only 11% relative to current practice.

Characterizing sliding wear behavior of A1100/AlFe (p) composites produced via repeated fold-forging and annealing

Abstract Aluminum matrix/aluminum-iron intermetallic composite materials pose challenges in plastic processing due to the susceptibility of hard intermetallic compound particles to fracture. This study introduces a novel fabrication method involving pure iron mesh, hot-dip aluminum plating, and solidification. Through ten consecutive folding, forging, and intermediate annealing cycles, aluminum matrix and iron undergo diffusion, leading to the formation of Fe2Al5 and FeAl3 interface reaction layers, as confirmed by X-ray diffraction analysis. Subsequent forging cycles cause the breakage or detachment of Fe2Al5 and FeAl3 particles from the interface, resulting in the formation of large-sized Fe2Al5 and small-sized Fe2Al5 intermetallic particles. FeAl3 intermetallic particles are observed via microscopic examination. These particles can be uniformly dispersed within the aluminum matrix through plastic flow, enabling the successful fabrication of A1100/Fe2Al5 and AlFe3 composite sheets. Furthermore, the study investigates the impact of intermetallic compound content, sliding speed, and forward load on the dry sliding wear of A1100/FeAl composites. It is found that Fe2Al5 and AlFe3 intermetallic compound particles effectively mitigate adhesive wear, plowing, and oxidative wear of the composites. With an AlFe intermetallic compound content of 4.3 wt.%, the volume wear rate remains low under conditions corresponding to PV = 56.652 (equivalent to a normal load of 19.6 kPa and a sliding speed of 2.87 m s−1).

VUV Activated Fe(VI) by Promoting the Generation of Intermediate Valent Iron and Hydroxyl Radicals.

In this study, vacuum ultraviolet (VUV) was first proposed to activate ferrate (Fe(VI)) for degrading micropollutants (e.g., carbamazepine (CBZ)). Results indicated that VUV/Fe(VI) could significantly facilitate the CBZ degradation, and the removal efficiencies of VUV/Fe(VI) were 30.9-83.4% higher than those of Fe(VI) at pH = 7.0-9.0. Correspondingly, the degradation rate constants of VUV/Fe(VI) were 2.3-36.0-fold faster than those of Fe(VI). Free radical quenching and probe experiments revealed that the dominant active species of VUV/Fe(VI) were •OH and Fe(V)/Fe(IV), whose contribution ratios were 43.3 to 48.6% and 48.2 to 46.6%, respectively, at pH = 7.0-9.0. VUV combined with Fe(VI) not only effectively mitigated the weak oxidizing ability of Fe(VI) under alkaline conditions (especially pH = 9.0) but also attenuated the deteriorating effect of background constituents on Fe(VI). In different real waters (tap water, river water, WWTPs effluent), VUV/Fe(VI) retained a remarkably enhanced effect on CBZ degradation compared to Fe(VI). Moreover, VUV/Fe(VI) exhibited outstanding performance in the debasement of CBZ and sulfamethoxazole (SMX), as well as six other micropollutants, displaying broad-spectrum capability in degrading micropollutants. Overall, this study developed a novel oxidation process that was efficient and energy-saving for the rapid removal of micropollutants.

Understanding Variations in Ferrate Detection through the ABTS Method in the Presence of Electron-Rich Organic Compounds.

The chromogenic reaction between 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) and ferrate [Fe(VI)] has long been utilized for Fe(VI) content measurement. However, the presence of electron-rich organic compounds has been found to significantly impact Fe(VI) detection using the ABTS method, leading to relative errors ranging from ∼88 to 100%. Reducing substances consumed ABTS•+ and resulted in underestimated Fe(VI) levels. Moreover, the oxidation of electron-rich organics containing hydroxyl groups by Fe(VI) could generate a phenoxyl radical (Ph•), promoting the transformation of Fe(VI) → Fe(V) → Fe(IV). The in situ formation of Fe(IV) can then contribute to ABTS oxidation, altering the ABTS•+:Fe(VI) stoichiometry from 1:1 to 2:1. To overcome these challenges, we introduced Mn(II) as an activator and 3,3',5,5'-tetramethylbenzidine (TMB) as a chromogenic agent for Fe(VI) detection. This Mn(II)/TMB method enables rapid completion of the chromogenic reaction within 2 s, with a low detection limit of approximately 4 nM and a wide detection range (0.01-10 μM). Importantly, the Mn(II)/TMB method exhibits superior resistance to reductive interference and effectively eliminates the impact of phenoxyl-radical-mediated intermediate valence iron transfer processes associated with electron-rich organic compounds. Furthermore, this method is resilient to particle interference and demonstrates practical applicability in authentic waters.

Uniformly deposition of iron phosphide quantum dots on the microscopic spongy B-C3N4 and its efficient degradation of ciprofloxacin by photo-self-Fenton process

In this research, iron phosphide quantum dots (FeP QDs) are synthesized and anchored on the microporous spongy BxCN uniformly through a novel hydrothermal-phosphorization processes. FeP@BxCN shows excellent photo-self-Fenton capability and applies to eliminate CIP from aqueous solution. Results indicate both photocatalysis and self-Fenton processes contribute to CIP degradation (photocatalysis: 69.1 %; self-Fenton: 28.2 %). The decoration of FeP QDs could effectively suppress the recombination of photogenerated carriers and improve the photocatalysis performance. They also accelerate the transformation of in situ H2O2 to •OH radicals thus enhance the efficiency of self-Fenton process. Furthermore, FeP QDs shows pretty low consumption during the self-Fenton process because of the regeneration mechanism between cationic iron species, H2O2 and anionic phosphorus. The existence of intermediate valence iron (Feɛ+) and anionic phosphorus (Pɛ-) ensured the regeneration of Fe(II) and the circulation between Fe(II), Feɛ+ and Fe(III). Optimal CIP degradation efficiency could be achieved under neutral condition and the corresponding CIP removal efficiency are 97.3 % when the initial concentration is 30 mg•L−1 and reaction within 120 min. Results propose a meaningful exploration for antibiotics degradation via photocatalytic-self-Fenton technology.

Novel enhanced defluorination of perfluorooctanoic acids by biochar-assisted ultrasound coupling ferrate: Performance and mechanism

An ultrasound (US)/biochar (BC)/ferrate (Fe (VI)) system was firstly proposed to enhance perfluorooctanoic acid (PFOA) defluorination. It achieved 93 % defluorination optimally, higher than the sum of 77 % (28 % and 49 % for US/BC and US/Fe (VI) respectively), implying synergistic effect. Besides, the mechanism study confirmed that, this system can not only increase the specific surface area of BC and the generation of reactive oxidant species (ROS), enriching the active sites and forming new oxygen-containing functional groups, but also promote the formation of intermediate iron species. The PFOA degradation in the US/BC/Fe (VI) was probably an adsorption-degradation process, both ROS and electron transfer promoted the defluorination. Additionally, its sustainability was also demonstrated with 14 % reduced defluorination percentage after five cycles of BC. Overall, the synergistic effect of the US/BC/Fe (VI) and its enhancing mechanism for PFOA defluorination were clarified firstly, which contributes to the development of biochar for assisting polyfluoroalkyl substances degradation.

Iron-doped carbon nanotubes with magnetic enhanced Fe(VI) degradation of arsanilic acid and inorganic arsenic: Role of intermediate iron species and electron transfer

Arsanilic acid (p-AsA), a prevalently used feed additive, is frequently detected in environment posing a great threat to humans. Potassium ferrate (Fe(VI)) was an efficient way to tackle arsenic contamination under acid and neutral conditions. However, Fe(VI) showed a noneffective removal of p-AsA under alkaline conditions due to its oxidation capacity attenuation. Herein, a magnetic iron-doped carbon nanotubes (F-CNT) was successfully prepared and further catalyzed Fe(VI) to remove p-AsA and total As species. The Fe(VI)/F-CNT system showed an excellent capability to oxidize p-AsA and adsorb total As species over an environment-related pH range of 6–9. The high-valent iron intermediates Fe(V)/Fe(IV) and the mediated electron-transfer played a significant part in the degradation of p-AsA according to the probes/scavengers experiments and galvanic oxidation process. Moreover, the situ formed iron hydroxide oxide and F-CNT significantly improved the adsorption capacity for total As species. The electron-donating groups (semiquinone and hydroquinone) and high graphitization of F-CNT were responsible for activating Fe(VI) based on the analysis of X-ray photoelectron spectroscopy (XPS). Density functional theory calculations and the detected degradation products both indicated that the amino group and the C–As bond of p-AsA were main reactive sites. Notably, Fe(VI)/F-CNT system was resistant to the interference from Cl−, SO42−, and HCO3−, and could effectively remove p-AsA and total As species even in the presence of complex water matrix. In summary, this work proposed an efficient method to use Fe(VI) for degrading pollutants under alkaline conditions and explore a new technology for livestock wastewater advanced treatment.

Enhanced Oxidation of Organic Compounds by the Ferrihydrite-Ferrate System: The Role of Intramolecular Electron Transfer and Intermediate Iron Species.

Previous studies mostly held that the oxidation capacity of ferrate depends on the involvement of intermediate iron species (i.e., FeIV/FeV), however, the potential role of the metastable complex was disregarded in ferrate-based heterogeneous catalytic oxidation processes. Herein, we reported a complexation-mediated electron transfer mechanism in the ferrihydrite-ferrate system toward sulfamethoxazole (SMX) degradation. A synergy between intermediate FeIV/FeV oxidation and the intramolecular electron transfer step was proposed. Specifically, the conversion of phenyl methyl sulfoxide (PMSO) to methyl phenyl sulfone (PMSO2) suggested that FeIV/FeV was involved in the oxidation of SMX. Moreover, based on the in situ Raman test and chronopotentiometry analysis, the formation of the metastable complex of ferrihydrite/ferrate was found, which possesses higher oxidation potential than free ferrate and could achieve the preliminary oxidation of organics via the electron transfer step. In addition, the amino group of SMX could complex with ferrate, and the resulting metastable complex of ferrihydrite/ferrate would combine further with SMX molecules, leading to intramolecular electron transfer and SMX degradation. The ferrate loss experiments suggested that ferrihydrite could accelerate the decomposition of ferrate. Finally, the effects of pH value, anions, humic acid, and actual water on the degradation of SMX by ferrihydrite-ferrate were also revealed. Overall, ferrihydrite demonstrated high catalytic capacity, good reusability, and nontoxic performance for ferrate activation. The ferrihydrite-ferrate process may be a green and promising method for organic removal in wastewater treatment.

Enhanced removal of organic arsenic by using potassium ferrate coupled with metal coagulants: Role of iron species and effect of AlCl3 and FeCl3

This study investigated the removal performance and synergistic mechanism of p-arsanilic acid (p-ASA) using a pre-oxidative coagulation system of potassium permanganate (K2FeO4) with aluminum chloride (AlCl3) or ferric chloride (FeCl3). The arsenic removal efficiencies of K2FeO4-AlCl3 and K2FeO4-FeCl3 reached 93.46% and 98.58%, respectively. K2FeO4 could alter the distribution of hydrolysis products of the coagulants and the addition of the coagulants directly or indirectly influenced the generation of intermediate valence iron (Fe(IV) and Fe(V)), interestingly, the mechanisms of aluminum and iron salts enhancing the removal of p-ASA by potassium ferrate were different. During the coupling process, AlCl3 and FeCl3 enhanced the self-decomposition rate of K2FeO4 with △kAl = 3.0530 and △kFe = 0.0912, respectively, resulting in difference on the generation of Fe(IV) and Fe(V). FeCl3 facilitated more effective Fe(IV) and Fe(V) production (FeCl3eff/AlCl3eff＞1), and multiple active iron species degraded p-ASA into inorganic arsenic, p-aminophenol (p-AP), nitarsone (NIA), and other products. Additionally, in the presence of K2FeO4, the hydrolytic dominant species of AlCl3 and FeCl3 were influenced under near-neutral conditions (pH 6–8), and Al13 and polynuclear Fe-hydroxides (PnFe-H) effectively improved the removal efficiency of inorganic arsenic and other organic products. The in-situ generation of nanoiron particles by K2FeO4 altered the original floc structure of the coagulants, with the specific surface areas of the flocs being 8733.176 cm2/cm3 for K2FeO4-AlCl3 and 7232.856 cm2/cm3 for K2FeO4-FeCl3. The coupling of K2FeO4 with metal salt coagulants not only enhanced p-ASA removal but also effectively improved the floc structure.

An S=1 Iron(IV) Intermediate Revealed in a Non‐Heme Iron Enzyme‐Catalyzed Oxidative C−S Bond Formation

AbstractErgothioneine (ESH) and ovothiol A (OSHA) are two natural thiol‐histidine derivatives. ESH has been implicated as a longevity vitamin and OSHA inhibits the proliferation of hepatocarcinoma. The key biosynthetic step of ESH and OSHA in the aerobic pathways is the O2‐dependent C−S bond formation catalyzed by non‐heme iron enzymes (e.g., OvoA in ovothiol biosynthesis), but due to the lack of identification of key reactive intermediate the mechanism of this novel reaction is unresolved. In this study, we report the identification and characterization of a kinetically competent S=1 iron(IV) intermediate supported by a four‐histidine ligand environment (three from the protein residues and one from the substrate) in enabling C−S bond formation in OvoA from Methyloversatilis thermotoleran, which represents the first experimentally observed intermediate spin iron(IV) species in non‐heme iron enzymes. Results reported in this study thus set the stage to further dissect the mechanism of enzymatic oxidative C−S bond formation in the OSHA biosynthesis pathway. They also afford new opportunities to study the structure‐function relationship of high‐valent iron intermediates supported by a histidine rich ligand environment.

An S=1 Iron(IV) Intermediate Revealed in a Non-Heme Iron Enzyme-Catalyzed Oxidative C-S Bond Formation.

Ergothioneine (ESH) and ovothiol A (OSHA) are two natural thiol-histidine derivatives. ESH has been implicated as a longevity vitamin and OSHA inhibits the proliferation of hepatocarcinoma. The key biosynthetic step of ESH and OSHA in the aerobic pathways is the O2 -dependent C-S bond formation catalyzed by non-heme iron enzymes (e.g., OvoA in ovothiol biosynthesis), but due to the lack of identification of key reactive intermediate the mechanism of this novel reaction is unresolved. In this study, we report the identification and characterization of a kinetically competent S=1 iron(IV) intermediate supported by a four-histidine ligand environment (three from the protein residues and one from the substrate) in enabling C-S bond formation in OvoA from Methyloversatilis thermotoleran, which represents the first experimentally observed intermediate spin iron(IV) species in non-heme iron enzymes. Results reported in this study thus set the stage to further dissect the mechanism of enzymatic oxidative C-S bond formation in the OSHA biosynthesis pathway. They also afford new opportunities to study the structure-function relationship of high-valent iron intermediates supported by a histidine rich ligand environment.

The Effect of Iron Overload on the Mobilization of Peripheral Blood Hematopoietic Stem Cells in Pediatric Patients with Thalassemia Major

Introduction: The purpose of this study was to examine the effect of iron overload on the mobilization of peripheral blood stem cells (PBSCs) in pediatric patients with β-thalassemia major (TM). Methods: We retrospectively reviewed the records of 226 patients with TM from whom PBSCs were collected. Iron overload was based on serum ferritin level, and liver and cardiac iron overload was measured by magnetic resonance imaging (MRI) T2*. Results: The mean age of the TM patients was 7.35 ± 3.41 years. Of the patients, only 171 received MRI. Of the 171 patients, 35 had normal liver iron levels, 39 mild liver iron overload, 90 intermediate liver iron overload, and 7 severe liver iron overload. The intermediate + severe group was associated with significantly higher age and BMI and lower leukapheresis product white blood cell count and CD34⁺ cell levels (all, p < 0.05). Conclusion: Leukapheresis indices were similar between patients with different degrees of iron overload according to the ferritin level and cardiac iron overload, in which the later might be due to the small number of patients with cardiac overload. In patients with TM, the intermediate and severe liver iron overload was associated with poorer mobilization of PBSCs.

Enhanced ferrate(VI) oxidation of organic pollutants through direct electron transfer

Fe(VI) is a versatile agent for water purification, and various strategies have been developed to improve its pollutant removal efficiency. Herein, it was found that in addition to intermediate iron species [Fe(IV)/Fe(V)], direct electron transfer (DET) played a significant role in the abatement of organic pollutants in Fe(VI)/carbon quantum dots (CQDs) system. Around 86, 83, 73, 64, 52, 45 and 17% of BPA, DCF, SMX, 4-CP, phenol, p-HBA, and IBP (6 μM) could be oxidized by 30 μM of Fe(VI), whereas with the addition of CQDs (4 mg/L), the oxidation ratio of these pollutants increased to 98, 99, 80, 88, 87, 66 and 57%, respectively. The negative impact induced by solution pH and background constituents on Fe(VI) abatement of pollutants could be alleviated by CQDs, and CQDs acted as catalysts for mediating DET from organic pollutants to Fe(VI). Theoretical calculation revealed that iron species [Fe(VI)/Fe(V)/Fe(IV)] was responsible for the oxidation of 36% of phenol, while DET contributed to the oxidation of 64% of phenol in the Fe(VI)/CQDs system. Compared with iron species oxidation, the CQDs mediated DET from pollutants to Fe(VI) was more efficient for utilizing the oxidation capacity of Fe(VI). The DET mechanism presented in the study provides a prospective strategy for improving the pollution control potential of Fe(VI).

High-speed imaging and statistics of puffing and micro-exploding droplets in spray-flame synthesis

Thermally-induced breakup of metal-precursor-laden droplets in spray-flame synthesis occurs via a rapid and disruptive disintegration, i.e., “puffing” and “micro-explosion”. To assess the temporal evolution and statistics of droplet disruption, LED-illuminated droplet shadowgraphs were imaged with a microscope onto a high-speed camera and morphological image analysis was applied. The atomized liquid was a mixture of 35 vol.-% ethanol and 65 vol.-% 2-ethylhexanoic acid mixed with iron(III) nitrate nonahydrate (INN) as a precursor. Droplet evaporation and disruption were also simulated with a population balance model. The model finds solid precipitates forming in the droplets because of the decomposition of the precursor intermediate iron(III) 2-ethylhexanoate. The precipitates form a particle shell, which favors the superheating of the droplets’ interior, and they facilitate heterogeneous bubble nucleation. Imaging experiments and modelling find that per 10 µs lifetime of a droplet, the probability for disruption increases from 5 to 13% and 5 to 19%, respectively, when increasing the INN concentration from 0.05 to 0.5 mole/l. The probability of disruption suggests that throughout their lifetime in the spray flame, nearly all droplets will undergo disruption and many of them multiple times. In the experiment, droplets before disruption are 15% smaller than regular, non-disrupting droplets. Once disrupted, the droplets have a 45% smaller mean diameter than regular droplets. Under all conditions, disrupting and disrupted droplets are slower than regular droplets while the disruption does not significantly accelerate disrupted droplets.

Enantioselective and Enantioconvergent Iron‐Catalyzed C(sp3)‐H Aminations to Chiral 2‐Imidazolidinones

Comprehensive SummaryEnantioselective or enantioconvergent iron‐catalyzed ring‐closing C(sp3)‐H aminations of N‐aroyloxyurea through intermediate iron nitrene species provide chiral 2‐imidazolidinones in up to 99% yield and with up to 95% ee (40 examples). This is a rare example in which sustainable iron catalysis is combined with C(sp3)‐H amination and asymmetric catalysis. Chiral 2‐imidazolidinones are prevalent structural motifs in bioactive molecules and can also be hydrolyzed to valuable chiral vicinal diamines in a single step.

Zero valent copper-mediated ferrate (Ⅵ) for the degradation of bisphenol AF

This study presented a novel zero valent copper-mediated ferrate (VI) oxidation system for the degradation of bisphenol AF (BPAF). The effect of various factors (such as the dosage of ZVC, the concentration of ferrate(VI), the reaction temperature, the initial pH of reaction solution, inorganic anions and HA) on the BPAF degradation process was investigated. It was discovered that ZVC had a good catalytic effect on ferrate(VI), with a removal efficiency of 92.4% achieved in 3 min under a standard condition([ZVC]0 =50 mg/L, [Fe(Ⅵ)]0 = 30 μM, [BPAF]0 = 3 μM, [pH]0 = 7, T = 25 ℃). Nitrate ions (NO3-) have no obvious effect on the degradation of BPAF. Sulfate ions (SO42-) promoted BPAF degradation at low concentrations but inhibited it at high concentrations, whereas different concentrations of chloride (Cl-) or bicarbonate ions (HCO3-) inhibited it. Furthermore, methyl phenyl sulfoxide (PMSO) was used as a probe to detect the presence of active species in this system. The results showed that the intermediate iron substances (Fe(IV)/Fe(V)) with strong oxidation ability and Fe(VI) completed the degradation of BPAF collectively. The use of zero-valent copper and ferrate (VI) provided a viable method for removing refractory organics from wastewater.

Development of thermally stable carbon nanotube tapes by incorporating FeCl3

An effective process for incorporating FeCl3 into carbon nanotube (CNT) tapes is reported that harnesses high electrical conductivity and thermal stability. By actively introducing a controlled oxidation process, the intermediate iron species FeCl2(H2O)4, responsible for providing the high-temperature tolerance to CNT tapes, was successfully stabilized to increase the oxidative decomposition of CNTs by 75 °C, as compared with their unmodified counterparts. Thermal and structural characterizations revealed that the transformed FeCl2(H2O)4 was located inside the CNTs. This result expands the application of CNT tapes, as good lightweight and flexible conductors, for high-temperature industrial applications.

The Association between Dietary Iron Intake and Incidence of Dementia in Adults Aged 60 Years or over in the UK Biobank.

Background Several studies have investigated the association between dietary iron intake and cognitive impairment, but little is known about the relationship between iron intake and dementia incidence. Objectives This study explored the association between dietary iron intake and incident dementia in males and females. Whether this association was modified by factors such as age and medical diseases was also examined. Methods We included 41,213 males and 48,892 females aged 60 years or over, from the UK-Biobank cohort. Dietary iron intake was measured using a web-based 24-h dietary recall questionnaire from between 2009 and 2012. Incident dementia was ascertained using hospital inpatient records and death registers until April 2021. Cox proportional regression models examined the association between iron intake and incident dementia, and hazard ratio curves were constructed with knots from the analysis indicating insufficient or excessive iron intake. Results During a mean follow-up of 11.8 years, 560 males and 492 females developed dementia. A non-linear relationship between iron intake and incident dementia was observed in both males and females. The lowest incidence rates were observed in the higher iron intake quintile (Q4: ≥15.73, <17.57 mg/day) for males, and the intermediate iron intake quintile (Q3: ≥12.4, <13.71 mg/day) for females. Among those aged 60 and above, all-cause dementia in males was associated with deficient iron intake (Q1 versus Q4: Hazard ratio [HR]: 1.37, 95% Confidence interval [95%CI]: 1.01−1.86, p = 0.042) and excessive iron intake (Q5 versus Q4: HR: 1.49, 95%CI: 1.14−1.96, p = 0.003), whilst significant associations between all-cause dementia and deficient iron intake were only observed in females without hypertension. Smoking status was a significant moderator (p-value for trend = 0.017) for dementia in males only. Conclusions Excessive iron intake (≥17.57 mg/day) is associated with a higher incidence of all-cause dementia in males and smoking status modified this association amongst males. Deficient iron intake (<10.93 mg/day) was associated with a higher incidence of all-cause dementia in females without a history of hypertension.

Germanium hydrides as an efficient hydrogen-storage material operated by an iron catalyst.

The use of metal hydrides such as NaBH4 as hydrogen-storage materials has recently received substantial research attention on account of the worldwide demand for the development of efficient hydrogen-production, -storage, and -transportation systems. Here, we report the quantitative production of H2 gas from a germanium hydride, Ph2GeH2, mediated by an iron catalyst at room temperature via dehydrogenative coupling, concomitant with the formation of (GePh2)5. Of particular importance is that Ph2GeH2 can be facilely recovered from (GePh2)5 by contact with 1 atm of H2 or PhICl2/LiAlH4 at 0 °C or 40 °C, respectively. A detailed reaction mechanism for the iron-catalyzed dehydrogenative coupling of Ph2GeH2 is proposed based on the isolation of four intermediate iron species.

Improvement of Fe(VI) oxidation by NaClO on degrading phenolic substances and reducing DBPs formation potential

Ferrate(VI) is a green oxidant and can effectively oxidize micropollutants. However, the instability of Fe(VI), i.e., self-decomposition, in the aqueous solution limited its application. Herein, it was found that the degradation of phenolic substances had been substantially improved through the combination of Fe(VI) with NaClO. At the condition of pH 8.0, 50 μM of Fe(VI) degraded 18.66 % of BPA (bisphenol A) at 0.5 min or 21.67 % of phenol at 2 min. By contrast, Fe(VI)/NaClO (50/10 μM) oxidized 38.21 % of BPA at 0.5 min or 38.08 % of phenol at 2 min with a synergistic effect. At the end of the reaction, the concentration of Fe(VI) in Fe(VI)/NaClO (50/10 μM) was 28.97 μM for BPA degradation, higher than the 25.62 μM of Fe(VI) group. By active species analysis, intermediate iron species [i.e., Fe(V) and Fe(IV)] played a vital role in the synergistic effect in Fe(VI)/NaClO system, which would react with the applied NaClO to regenerate Fe(VI). In natural water, the Fe(VI)/NaClO could also degrade phenolic substances of natural organic matter (NOM). Although the NaClO reagent was applied, disinfection by-products (DBPs) formation potential decreased by 22.75 % of the raw sample after Fe(VI)/NaClO treatment. Significantly, THMs, mainly caused by phenolic substances of NOM, even declined by 29.18 % of raw sample. Based on that, this study explored a novel ferrate(VI) oxidation system using the cheap NaClO reagent, which would present a new insight on ferrate(VI) application.