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PHYSICA STATUS SOLIDI A-APPLICATIONS AND MATERIALS SCIENCE · 2024 ·Vol. 221 ·期 12 ·2300874 · IF 1.9

Fe-La-Ce-ZSM-5 Zeolite for Adsorbing Congo Red

Jie Yang,Zhengkun Cai,Dong Li

In this experiment, ZSM-5 molecular sieves are prepared by hydrothermal synthesis and modified by impregnation with Fe, La, and Ce loading. X-ray diffraction, X-ray photon-electron spectroscopy, and scanning electron microscopy show that Fe, La, and Ce elements are successfully loaded onto the surface of the material, and the surface area of Fe-La-Ce-ZSM-5 is 241.66 m 2 g −1 . A systematic study on the adsorption of Congo red solution is carried out using Fe-La-Ce-ZSM-5 molecular sieves and it is found through the adsorption data that the adsorption process is more in line with Langmuir and the proposed second-order kinetic model, and the theoretical saturated adsorption capacity is 2669.19 mg g −1 . The adsorption process is recycled four times and still has more than 60 % removal performance for high-concentration Congo red solution. The results of this experiment show that Fe-La-Ce-ZSM-5 molecular sieves show excellent removal performance for Congo red dye in wastewater.

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Advanced Energy Materials · 2024 · IF 24.4

Multihybridization for Enhancing Fe-Ni Bimetal Electrocatalyst in Water Oxidation

Hongyan Zhang,Hao Zhou,Hua Wang,Yikai Wang,Xuehan Yang,Dan Wu,Pan Yuan,Maoshuai He,Wenxian Wei,Tao Yang

Water electrolysis holds the promise of transforming electric-power into hydrogen energy through a carbon free process and its widespread application highly depends on anodic oxygen evolution reaction (OER) efficiency. Transition metal-based OER catalysts meet the requirements of long-term development for cost effectiveness, and their performance can be improved by a variety of band electronic structure modulating methods. Herein, a multihybridization strategy is proposed, i.e., p-d, s-sp , and d-d hybridization are emphasized together, which guides the design of an effective vanadium (V), boron (B)-FeNiP catalyst. Density functional theory analysis reveals the existence of multihybridization and the difference between Fe and Ni in terms of hybridization strength, band configuration, and interfacial charge transfer. Specially, Fe and Ni sites are simultaneously optimized to their highest performance upon the dual B, V incorporation. As a result, the VB-FeNiP catalyst displays outstanding OER performance, regarding a Tafel slope of 57.64 mV dec −1 , an overpotential of 175 mV at 100 mA cm −2 , and exceptional stability. Here the synergistic effect of multihybridization in the design of transition metal-based catalysts is highlighted and the work in pursuit of effective way based on regulating band configuration to developing high performance OER catalysts would be evoked.

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CHEMOSPHERE · 2017 · IF 4.208

Trimethoprim degradation by Fenton and Fe(II)-activated persulfate processes

Shizong Wang,Jianlong Wang

Trimethoprim is a pollutant ubiquitous in the environment due to its extensive application, and it cannot be effectively removed by conventional wastewater treatment processes . In this study, the Fenton and the Fe(II)-activated persulfate processes were employed to degrade trimethoprim in an aqueous solution. The results showed that the concentration of persulfate, H 2 O 2 and Fe(II) a had significant influence on the degradation of trimethoprim in both processes. De-ionized water spiked with trimethoprim resulted in the complete degradation of trimethoprim (0.05 mM) by the mineralization of 54.9% of Fenton's reagent when the concentrations of H 2 O 2 and Fe(II) were 1 mM and 0.05 mM, respectively. In contrast, 73.4% of trimethoprim was degraded by the mineralization of 40.5% of the Fe(II)-activated persulfate process when the concentration of persulfate and Fe(II) were each 4 mM. Intermediate compounds with different m / z were detected for the Fenton and the Fe(II)-activated persulfate processes, indicating alternative degradation pathways. In the actual wastewater spiked with trimethoprim, the removal efficiency of trimethoprim decreased to 35.8% and 43.6%, respectively, for the Fenton and the Fe(II)-activated persulfate processes. In addition, the decomposition efficiencies for hydrogen peroxide and persulfate were 43.8% and 92.5%, respectively, which was lower than those in the de-ionized water system. These results demonstrated that wastewater components had a negative influence on trimethoprim degradation and the decomposition of the oxidants (persulfate and H 2 O 2 ). In summary, the Fe(II)-activated persulfate process could be used as an alternative technology for treating trimethoprim-containing wastewater.

CAS / MDL: 738-70-5 14481-26-6
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LANGMUIR · 2025 · IF 3.9

Preparation and Photocatalytic Degradation of Fe-Doped BiOCl Photocatalytic Materials

Longqiang He,Xiaohua Wang,Dapeng Hong

Fe-doped BiOCl (Fe-BiOCl) hierarchical microspheres were successfully prepared by using a simple one-step solvothermal approach. The Fe-BiOCl hierarchical microspheres were analyzed by XRD, IR, SEM, XPS, TEM, etc. The analyses confirmed that impurity levels were successfully introduced into the band gap of BiOCl through Fe doping, leading to a decrease in the band gap and an expansion of the light absorption range to the visible region. Moreover, the separation and transfer of photogenerated carriers were more effectively promoted by Fe doping, resulting in a substantially elevated photocatalytic performance of BiOCl. After 40 min of dark adsorption and 60 min of photocatalysis, the removal efficiency of the prepared Fe-BiOCl-3 for methylene blue reached 93.5%, and the degradation reaction was accorded with a first-order kinetic law. After 5 cycles of photodegradation, Fe-BiOCl-3 still maintained its high photocatalytic ability, indicating that it had a certain degree of reusability. The active species capture experiment demonstrated that •O2– and •OH played a predominant role during the photocatalytic degradation process. Combined with the active species capture experiment, the photocatalytic degradation mechanism of Fe-BiOCl-3 was put forward.

CAS / MDL: 10035-06-0 7782-61-8
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MOLECULES · 2025 ·Vol. 30 ·期 11 ·2331 · IF 4.6

Multisite Fe3+ Luminescent Centers in the LiGaO2:Fe Nanocrystalline Phosphor

Ajeesh Kumar Somakumar,Ivo Romet,Agnieszka Grabias,Marcin Kruk,Shusaku Hayama,Damian Wlodarczyk,Justyna Barzowska,Yadhu Krishnan Edathumkandy,Eduard Feldbach,Puxian Xiong,Yaroslav Zhydachevskyy,Monika Trzaskowska,Hanka Przybylinska,Andrzej Suchocki

An extensive experimental study of trivalent iron (Fe3+) ions in orthorhombic lithium gallate nanocrystals was undertaken. Various spectroscopic methods, such as Raman spectroscopy, extended X-ray absorption fine structure, the Mössbauer effect, electron paramagnetic resonance, photoluminescence, thermoluminescence, and cathodoluminescence were used to investigate the synthesized phosphor. This study revealed the existence of multiple Fe3+sites, out of which the tetrahedral sites are preferentially occupied. Extensive optical studies showed that the Fe3+doped lithium gallate phosphor is a promising candidate for various luminescence and thermoluminescence-related applications in the near-infrared regime.

CAS / MDL: 12024-21-4 554-13-2
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Formation mechanism of Fe-based multi-catalysts for growing CNTs

Peng Wang,Chenyu Gao,Qianpeng Dong,Lianlian Wang,Dianming Chu,Yan He,Wenjuan Bai

s The application of carbon nanotubes in materials science is rapidly expanding, leading to an increasingly urgent demand for large-scale synthesis. Central to the growth of carbon nanotubes is the development of effective catalysts; thus, the large-scale production of these catalysts becomes crucial for successful carbon nanotube synthesis. Extensive research has been conducted on the mechanisms and regulation of interfacial interactions between metals and supports during catalyst synthesis. This paper is based on the interface interactions between common metal catalysts such as Fe, Co, Ni, and Al 2 O 3 , and Fe-Co, Fe-Ni, and Fe-Co-Ni metal catalysts were prepared by a one-step method. The catalysts were synthesized through a "one-step process," and the formation mechanisms of bimetallic and trimetallic catalysts, as well as the influence of interfacial interactions on catalyst formation and catalytic activity, were thoroughly investigated. The results indicate that with the involvement of Fe, Co and Ni on the surface of Al 2 O 3 maintain a small size morphology due to interfacial interaction. Meanwhile, the nanoparticles form a doped structure with Al 2 O 3 , effectively avoiding the deactivation of nanoparticles caused by agglomeration. In addition, the three catalysts for growing CNTs were analyzed in order to investigate the effects of different concentrations of metal ratios and time of carbon source on the catalytic activity, which provides new ideas for improving the catalyst design system.

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Water Supply · 2020 ·Vol. 21 ·期 3 ·1016-1024 · IF 0.9

Formation of iodinated products in Fe (II)/peroxydisulfate (PDS) system

Dong Zijun,Li Mu,Chen Meifen,Gu Yurong,Jiang Chengchun,Sun Feiyun

The transformation of iodide (I − ) and hypoiodous acid (IO − ) by Fe (II)-activated peroxydisulfate (PDS) in the presence of natural organic matter (NOM) was investigated. In the water of a reservoir in Shenzhen, four kinds of organic matter were detected: iodoform > diiodo-bromomethane > dibromo-iodomethane > dichloromethane. As pH increased from 3 to 10, I − conversion rate decreased from 31.0% to 11.0%. There is basically no iodic acid ( ⁠ ⁠ ) generated under alkaline conditions, probably due to these organic matters. When PDS concentration is low, PDS can oxidize part of I − to IO − , and the oxidation of I − into reaction and continued oxidation reaction exist at the same time, so some is generated in the system. As the proportion of Fe (II) increases, the generation rate of gradually increases. When Fe 2+ /PDS is 1:5, 2:5, and 3:5, the conversion rates of are 4.7%, 6.5%, and 8.4%, respectively. There are two main reasons for this: (i) the reaction of IO − produced in the system with humic acid (HA) inhibits the further conversion of IO − to ⁠ ; (ii) both HA and I- in the system can react with PDS, resulting in a reduction in the oxidation rate of I − . Formation of I-DBPs by Fe (II)/PDS process in real water was evaluated. I-DBPs generation in various reaction conditions was examined. Existence of HA showed apparent inhibition on IO 3 − generation.

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CHEMICAL ENGINEERING JOURNAL · 2016 · IF 5.31

Efficient removal of bromate with core-shell Fe@Fe2O3 nanowires

Wenjuan Shen,Fangjing Lin,Xu Jiang,Hefei Li,Zhihui Ai,Lizhi Zhang

In this study, we systematically investigated the removal of bromate (BrO 3 − ) with core-shell Fe@Fe 2 O 3 nanowires at neutral pH, especially the effects of surface bound ferrous ions and molecular oxygen. In the presence of Fe@Fe 2 O 3 nanowires, bromate was reduced to Br − efficiently with the generation of HOBr intermediates. Bromide species analyses and nanowires characterizations indicated that surface bound ferrous ions of core-shell Fe@Fe 2 O 3 nanowires could effectively promote the BrO 3 − removal. Meanwhile, molecular oxygen competed electrons from both Fe 2+ and Fe 0 to generate reactive oxygen species of O 2 − , H 2 O 2 , and OH during the bromate removal process. Among the generated reactive oxygen species, O 2 − and H 2 O 2 favored of bromate removal, but OH inhibited. We proposed a bromate removal mechanism with core-shell Fe@Fe 2 O 3 nanowires, which suggested that the effect of surface bound Fe(II) and molecular oxygen was taken into consideration when using nZVI for bromate remediation in waters. This study can not only deepen our understanding on the bromate removal with zero valent iron, and also shed light on the design of high performance bromate removal materials.

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JOURNAL OF MEMBRANE SCIENCE · 2024 · IF 8.4

Low-cost iron (Fe) hollow fiber membrane for hydrogen separation

Zhifei Hu,Zejiao Wang,Mingming Wang,Zhigang Wang,Yuanyuan Chu,Xiaoyao Tan,Yunxia Hu,Tianjia Chen,Shaomin Liu

Dense metal membranes are widely studied due to their promising performance in hydrogen separation. In this work, the low-cost dense iron (Fe) hollow fiber membranes (FeHFMs) were developed via the phase inversion and high-temperature sintering method. By tuning the preparation conditions, two typical gas-tight hollow fibers referred to as the sandwich- and honeycomb-structured membranes were successfully synthesized. H 2 permeation behavior was well described by Sieverts equation based on the solution-diffusion mechanism. The sandwich-structured FeHFMs had an H 2 flux of up to 7.51 mmol m −2  s −1 when operated at a temperature of 850 °C. In comparison, the honeycomb-structured FeHFMs further enhanced the H 2 flux by a factor of 3.2 due to the optimized membrane morphology with only one single dense iron layer. The developed FeHFMs showed superior H 2 permeation stability in thermal shock tests (40 h) and long-term stability tests (120 h). This work also expanded the potential application horizons of the FeHFMs, which can be easily tailored into porous or dense structures by tuning the sintering conditions.

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GREEN CHEMISTRY · 2020 ·Vol. 22 ·期 24 ·8728-8733 · IF 9.48

Clean & environmentally friendly regeneration of Fe-surface cleaning pickling solutions

Qun Liu,Dan Pan,Tingting Ding,Mengchao Ye,Fengjiao He

The spent pickling solution, which comes from the pickling process of iron and steel, is indispensable in the manufacturing industry. Iron gets dissolved in the acid solution during the pickling process. When the concentration of metal ions in the acid solution accumulates to a certain value, it cannot to be used to wash iron and steel materials and becomes spent pickling solution that should be treated before discharge. At present, spent pickling solutions are treated via neutralization precipitation techniques in industries. This treatment method has a large discharge of wastewater, and the cost is high due to which it cannot meet the needs of green cycle in industry production. In this study, a new method, which is based on the formation of quaternary ammonium salt precipitate in a strong acid solution, is proposed to treat the spent pickling solution. The spent pickling solution was recycled and reused by precipitation separation of iron ion. The quaternary ammonium salt was recycled by dissolving the obtained precipitate in an alkali solution. The new ferric hydroxide precipitate formed and quaternary ammonium salt was returned to the solution. In the whole process, only a few amount of alkali was consumed. The removal rate of iron ion was up to 99.72%. Compared with the traditional neutralization precipitation method, the acid is not consumed and it can be reused; the alkali was consumed only for the precipitation of iron ions, not for the neutralization of the acid. The proposed method is an effective and economic method for the recovery of the spent pickling solution. It is expected to satisfy the requirements of green cycle and environmental protection in industry production.

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ACS Sustainable Chemistry & Engineering · 2022 · IF 9.224

Electrochemically Activated Ni-Fe Oxyhydroxide for Mimic Saline Water Oxidation

Shusheng Wan,Xiaojun Wang,Guiru Zhang,Yongcheng Wang,Jie Chen,Qiaoxia Li,Yixiao Zhang,Liwei Chen,Xiaoming Wang,Guang Meng,Kun Jiang

Utilizing renewable energy to produce green hydrogen from saline water electrolysis is becoming increasingly important yet is largely challenged by the sluggish oxygen evolution reaction kinetics, the competitive anodic chlorine evolution reaction, and the resultant electrode corrosion. Here, we report an electrochemically activated Ni-Fe oxyhydroxide catalyst that delivers an early onset potential of 1.51 V at 100 mA cm–2 within mimic saline water of 0.5 M NaCl + 1 M NaOH. During the electrochemical activation, ex situ X-ray radiation and in situ Raman characterizations reveal the structural reconstruction of amorphous Ni (oxy)hydroxide generation and electronic structure modulation from Fe intercalation. Headspace gas chromatography and iodine titration results confirm the ∼100% Faradaic efficiency toward O2 evolution on activated NiFeOxHy, whereas the long-term stability is assessed by an anion exchange membrane electrolyzer, demonstrating only 350 mV voltage decay during the 100 h continuous electrolysis at 500 mA cm–2.

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Water · 2017 ·Vol. 9 ·期 5 ·326 · IF 1.832

Effect of Fe and EDTA on Freshwater Cyanobacteria Bloom Formation

Ting Zhang,Jian He,Xingzhang Luo

Due to the fact that not all eutrophic lakes have cyanobacteria blooms, we hypothesized Fe may be another important limiting factor which regulates cyanobacteria bloom formation. We tested the hypothesis by batch cultures of bloom-forming Cyanobacterium,Microcystis aeruginosawith different ethylenediaminetetraacetic acid (EDTA)-Fe concentrations (0.5–6.0 mg/L), three levels of initial biomass, and excessive N and P (N = 4.2 mg/L, P = 0.186 mg/L) to simulate dynamically a cyanobacteria bloom in eutrophic conditions. The effect of EDTA and Fe uptake kinetics byM. aeruginosawere also examined. Results showedM. aeruginosagrowth rate positively correlated with EDTA-Fe concentration and negatively correlated with biomass. Maximal biomass ofM. aeruginosawas determined by Fe availability and initial biomass. EDTA could decrease both Fe availability and toxicity. Based on experimental results, a conceptual model of how Fe availability regulates cyanobacterial biomass in eutrophic lakes was developed. This study demonstrated bioavailable Fe is a potential limiting factor in eutrophic lakes that should be included in eutrophication management strategies.Keywords:Microcystis;eutrophication control;freshwater;Fe availability

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