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CHEMOSPHERE · 2020 · IF 5.778

Rapid degradation of dimethoate and simultaneous removal of total phosphorus by acid-activated Fe(VI) under simulated sunlight

Jinsuo Lu,Zhanguo Cui,Xiaoyong Deng,Zhijie Liang,Shouning Chai,Junyu Fan,Zhiqiang Zhang,Zhiwei Zhao

Ferrate (Fe(VI)) is usually effective for oxidizing a variety of organic pollutants within a few seconds, but some recalcitrant asorganophosphorus pesticides such as dimethoate require higher dose of Fe(VI) and inorganic phosphorus produced by mineralization is difficult to remove. In this study, acid-activated ferrate (Fe(VI)) was firstly used to degrade organophosphorus pesticides dimethoate and simultaneously remove total phosphorus (TP) from solution under simulated sunlight. At a Fe(VI):dimethoate molar radio of 15:1, dimethoate was almost completely removed within 20 min and 47% of TP in the solution was removed by the reduction product of Fe(VI) within 240 min. Electron paramagnetic resonance (EPR) and terephthalic acid (TA) fluorescence experiments showed that •OH radicals were continuously generated in the system, and •OH formation pathway was proposed. Importantly, the involvement of •OH in acid-activated Fe(VI) process was confirmed for the first time by EPR. In the acid-activated Fe(VI)/simulated sunlight system, the removal of dimethoate and TP gradually increased with the decrement of activation pH, whereas the increase of molar ratio of Fe(VI):dimethoate enhanced the removal of dimethoate and TP. The addition of inorganic anions (HCO 3 - and NO 2 - ) had obvious inhibitory effects on dimethoate and TP removal. Eight degradation products including O,O,S-trimethylphosphorothiate, omethoate and 2- S -methyl-(N-methyl) acetamide were determined by gas chromatography mass spectrometry (GC-MS) analysis, and two possible degradation pathways were proposed. The insights gained from this study open a new avenue to simultaneously degrade and remove organic contaminants .

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Nanomaterials · 2020 ·Vol. 10 ·期 9 ·1655 · IF 4.324

Molecularly Imprinting Polymers (MIP) Based on Nitrogen Doped Carbon Dots and MIL-101(Fe) for Doxorubicin Hydrochloride Delivery

Yuqiong Shi,Yuxuan Wang,Jinhua Zhu,Wei Liu,Md. Zaved H. Khan,Xiuhua Liu

MIL-based molecularly imprinted polymer (MIP) nanocomposites were successfully synthesized through a simple and versatile stirring auxiliary encapsulation method. MIP as a carrier has been applied to the highly efficient selective recognition and sustained release of doxorubicin hydrochloride (DOX). The adsorption mechanism and release behavior of[email protected]in vitro were also discussed. Adsorption studies showed that MIP using DOX as template had specific selectivity to DOX, and its optimal drug loading efficiency reached 97.99%. The adsorption isotherm accorded with Freundlich models. The cumulative release curve showed that at the conditions of pH 5.5 and 7.4, the nanomaterials have a slow-release effect on the release of DOX. In addition, the cytotoxicity and bioactivity of MIP nanoparticles on HepG2 and HL-7702 cell lines measured by MTT assay also proved their low toxicity and biological activity. The cell activity of HepG2 and HL-7702 incubated with MIP for 24 h was 69.9% and 76.07%, respectively. These results collectively illustrated that the MIP nano-materials synthesized in this study can be efficiently employed to the drug delivery systems.Keywords:MIP;nanocomposites;drug delivery;DOX;controlled release

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Inorganic Chemistry Frontiers · 2020 ·Vol. 7 ·期 4 ·889-896 · IF 5.958

Synthesis of Fe3C@porous carbon nanorods via carbonizing Fe complexes for oxygen reduction reaction and Zn–air battery

Yijie Zhang,Yong Zhao,Muwei Ji,Han-ming Zhang,Minghui Zhang,Hang Zhao,Mengsi Cheng,Jiali Yu,Huichao Liu,Caizhen Zhu,Jian Xu

Fe-Based electrocatalysts on carbon substrates are considered suitable candidates for applications in Zn–air batteries due to their favorable ORR performance. Herein, unique Fe3C@N-doped porous carbon nanorods have been synthesized using a soft template method and carbonization. The material proved to have a porous hetero-structure, which is advantageous in providing effective electrocatalysis performance for oxygen reduction reaction, providing broad prospects for the development of non-precious metal electrocatalysts and metal–air batteries. This catalyst used for oxygen reduction reaction exhibits a half-wave of 0.83 V, which is close to that of the commercial Pt/C catalyst. Using the as-prepared Fe3C@N-doped porous carbon nanorods, the open circuit potential and power density of a Zn–air battery has been measured as 1.42 V and 126.4 mW cm−2, respectively, which are better than those of the commercial Pt/C. This study presents a novel strategy to prepare Fe3C@N-doped porous carbon nanorods, which can be used as highly effective oxygen reduction reaction catalysts for Zn–air batteries.

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Chemical Engineering and Processing-Process Intensification · 2019 · IF 3.031

Degradation of indigo carmine by coupling Fe(II)-activated sodium persulfate and ozone in a rotor-stator reactor

Ziye Zhao,Lei Wang,Jinmeng Fan,Yunhua Song,Guangwen Chu,Lei Shao

Rotor-stator reactor (RSR), a novel high-gravity device, was employed in the O 3 /persulfate (PS)/Fe 2+ process to enhance the degradation of indigo carmine (IC) in simulated wastewater. It was found that IC degradation efficiency increased with the increase of Fe 2+ concentration, RSR rotation speed, O 3 concentration and gas-liquid ratio, but decreased with the increase of IC concentration and temperature. When the rotation speed of RSR increased from zero to 1200 rpm, IC degradation efficiency increased from 25.6% to 64.2%. Because of the synergetic effects of the oxidative species (O 3 , OH, SO 4 − etc.), IC degradation efficiency in the O 3 /PS/Fe 2+ process was significantly higher than that in the O 3 or PS/Fe 2+ process. The high IC degradation efficiency can also be attributed to the good micromixing effect of the RSR. When the O 3 /PS/Fe 2+ process in the RSR was adopted before the sequencing batch reactor activated sludge process , both IC and COD degradation efficiencies increased significantly as a result of the improved biodegradability of the IC wastewater. Furthermore, a possible degradation mechanism of IC in the O 3 /PS/Fe 2+ process was proposed.

CAS / MDL: 860-22-0
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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Enhanced degradation of triclosan in heterogeneous E-Fenton process with MOF-derived hierarchical Mn/Fe@PC modified cathode

Xiaolan Zhou,Dong Xu,Yuancai Chen,Yongyou Hu

Mn/Fe@porous carbon (PC) was successfully fabricated through a simple carbonization of Mn-doped MIL-53(Fe) precursor and used as cathode modification in hydroxyl radical ( OH) based heterogeneous electro-Fenton (hetero-EF) process for triclosan (TCS) degradation. With co-doping of bimetal (Mn and Fe) in porous carbon, Mn/Fe@PC could markedly enhance the electrocatalysis with low oxygen reduction potential, high electrochemical active area and low resistance. Mn/Fe@PC modified cathode showed high electrocatalytic activity, great stability and low energy consumption (1.92 kWh m −1 and 0.63 kWh log −1  m −3 ) for TCS degradation over a wide pH range. The complete TCS degradation within 120 min and a 56.9 ± 2.0% TOC removal within 240 min were achieved under the condition of current 40 mA and initial pH 3. Based on the CV curves, the more negative reductive peak of Fe and Mn revealed the kinetically beneficial regeneration of Fe II /Mn II/III in Mn/Fe@PC. The electron transfer between Fe II/III and Mn II/III/IV , together with the direct regeneration of Fe II / Mn II/III on the cathode, could markedly promote the utilization of H 2 O 2, eventually leading to facilitating TCS degradation. According to the GC–MS intermediates, the possible TCS degradation pathway was deduced, including hydroxylation and dehalogenation attacked by OH. Furthermore, the TCS degradation experiments were also performed in different water matrix including river water, tap water and municipal sewage, indicating the feasibility of the TCS degradation in actual waters with Mn/Fe@PC-CP cathode in hetero-EF process. The toxicity analysis indicated that the hetero-EF process could achieve the TCS degradation and toxicity reducing.

CAS / MDL: 3380-34-5 100-21-0
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JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

Ethylene glycol assisted synthesis of hierarchical Fe-ZSM-5 nanorods assembled microsphere for adsorption Fenton degradation of chlorobenzene

Qin Zhu,Jiaorong Yan,Qiguang Dai,Qingqing Wu,Yuanpu Cai,Jinyan Wu,Xingyi Wang,Wangcheng Zhan

A unique zeolite catalyst, Fe doped ZSM-5 microsphere assembled by uniform nanorod-like crystals with hierarchical pore structure, was successfully synthesized and applied for the adsorption and degradation of trace chlorobenzene (CB) in the presence of H 2 O 2 . The organic ferric salts as the precursors, ethylene glycol as a chelating/reducing agent and the dynamic two-stage temperature-varied hydrothermal technique, together made the synthesized hierarchical Fe-ZSM-5 nanorods assembled microspheres (FZ-CA-5EG) to be characterized by abundant highly dispersed and valency-controlled framework Fe 3+/2+ species. As a result of these features, the FZ-CA-5EG showed excellent ability of adsorption and degradation efficiency of CB, and enhanced durability due to negligible leaching of framework Fe species. Moreover, the hydroxyl radicals were determined as the main the reactive oxygen species of CB oxidation degradation, and a possible adsorption-oxidation degradation pathway was proposed.

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Molecular Catalysis · 2019 · IF 2.938

The controlled preparation and performance of Fe, Co-modified porous ceria nanorods for the total oxidation of propane

Qi Song,Rui Ran,Jiancai Ding,Xiaodong Wu,Zichun Si,Duan Weng

Porous ceria nanorods modified with Fe or Co were prepared via a hydrothermal method. The structural properties, catalytic activities for the total oxidation of propane, and catalytic mechanisms of these materials were systematically investigated by X-ray diffraction, Raman spectroscopy, N 2 adsorption–desorption, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, catalytic activity measurements and in situ Fourier transform infrared spectroscopy. Co-modified ceria exhibited the best catalytic activity during propane oxidation as well as enhanced reducibility due to the synergistic interactions between the Co and the CeO 2 support. Variations in the activating ability and reducibility of the catalysts resulted in the formation of distinctive intermediates during the catalytic process, and this explained the observed differences in catalytic performance.

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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2022 · IF 4.326

Design of Prussian Blue Analogue-Derived Magnetic Binary Ce–Fe Oxide Catalysts for the Selective Oxidation of Cyclohexane

Shuang Wei,Hao Li,Kexin Li,Ruirui Zhang,Guosheng Wang,Ruixia Liu

We report the fabrication of Ce–Fe oxides (CFOs) derived from Prussian blue analogues (PBAs) with different shapes of sphere (CFO-S), bipyramid (CFO-B), and flower (CFO-F), which are prepared by controlling the volume ratio of water and ethanol and the addition of deep eutectic solvents (DESs) to control the solvent environment using a modified coprecipitation method. The structure, morphology, and the surface properties of Ce–Fe oxides were investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). The catalytic performance of PBA-derived Ce–Fe oxides was evaluated for the oxidation of cyclohexane, which positively correlated with surface oxygen vacancy and the amount ratio of Ce/Fe. The conversion for cyclohexane of CFO-S and CFO-B was 9.03 and 9.25%, respectively. However, CFO-S had a higher selectivity for K/A-oil (cyclohexanone and cyclohexanol) of 81.8%, resulting from the exposed crystal plane (100) compared to CFO-B (75%). Besides, CFO-F was rich in the Fe2O3 crystal phase, which is beneficial for KA selectivity. It was found that Ce3+, Fe3+, and OV had an important influence on the activation of C–H bonds, which provides a reference for the design of efficient alkane oxidation catalysts.

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ANALYST · 2022 ·Vol. 148 ·期 1 ·146-152 · IF 5.227

Dual mimic enzyme properties of Fe nanoparticles embedded in two-dimensional carbon nanosheets for colorimetric detection of biomolecules

Jie Wang,Chenglong Zhao,Feijin Zhou,Hui Lu,Zhenhong Huang,Cheng Yao,Chan Song

The development of novel nanozymes is of great importance for the efficient analysis of biomolecules such as H2O2, glucose, and antioxidants in the diagnosis of some diseases. Herein, novel nanozymes based on Fe nanoparticles (NPs) encapsulated in 2D carbon nanosheets (denoted as Fe@CNs) were constructed and employed in the field of biosensing. Notably, Fe@CNs have intrinsic dual mimic enzyme properties. The colorless colorimetric substrate 3,3′,5,5′-tetramethylbenzidine (TMB) can be oxidized by Fe@CNs as oxidase- and peroxidase-like nanozymes, respectively. The generation of the oxidation state TMB (oxTMB) resulted from the presence of reactive oxygen species (ROS) which were produced by the catalytic decomposition of the dissolved oxygen or H2O2. Thus, a simple colorimetric biosensor was proposed to detect glutathione (GSH), H2O2, and glucose. In addition, the Fe@CN-based nanozymes also have excellent reusability in enzymatic catalysis. After separating from the sensing systems, Fe@CNs can be reused in other catalytic processes. This colorimetric method could be used as a universal sensing platform for the detection of antioxidants and H2O2-related bioanalysis. This work broadens the application of novel nanozymes in biosensing.

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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2022 · IF 4.326

Fe, Zn Co-Doped Porous Carbon Nanofiber-Based Rechargeable Zinc Air Batteries with Stable Operation over 1600 h

Zhonghuan Zhu,Pengbo Liu,Pingping Du,Bo Yu,Xiaopeng Li,Yong Wang,Li-Ping Lv

Rational design of effective non-noble metal-based electrocatalysts with high conductivity, abundant active sites, and superior stability for zinc–air batteries (ZABs) with long-term cycling ability is highly demanded. A suitable carrier that can provide a high specific surface and porous structure to facilitate the exposure of active sites and the diffusion of reactants, products, and charges is of great importance. Herein, one-dimensional (1D) Fe–Zn-doped porous carbon fibers (Fe–Zn@NCF) are prepared from a polymer fiber matrix encapsulated with Fe-doped ZIF-8 nanocrystals by pyrolysis. The Fe–Zn@NCF exhibits good performance toward the oxygen reduction reaction or oxygen evolution reaction. Impressively, the assembled ZAB with Fe–Zn@NCF as the catalyst delivers a maximum peak power density of 184.6 mW cm–2, excellent rechargeability with a round-trip efficiency of 66.5%, and stable operation over 1600 h (800 cycles). These excellent electrocatalytic performances can be attributed to the Fe/Zn-based dual catalytic active sites and the 1D carbon fiber support of the catalyst with a hierarchical porous structure, a large surface area, and high conductivity that can facilitate fast mass and electron transportation and maintain the structural stability of the catalyst during cycling.

CAS / MDL: 14024-18-1
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

MoS4-LDH: A dual centre Fe-based layered double hydroxide catalyst for efficient atrazine removal and peroxymonsulfate activation

Jawad Ali,Dan Li,Ajmal Shahzad,Muhammad Wajid Ullah,Jerosha Ifthikar,Muhammed Asif,Chen Yanan,Xie Lei,Zhuqi Chen,Songlin Wang

The Fe-based materials were considered very attractive for the treatment of wastewater using peroxymonosulfate (PMS) activation. However, the difficulties to restore the active Fe 2+ oxidation state restrict them to attained sustainable efficiency. In this work, a new strategy was introduced to accelerate the regeneration of Fe 2+ state through constructing an electron-rich MoS 4 2− centre in the inter-layers of FeMgAl layered double hydroxide (MoS 4 -LDH) catalyst. The dual centre MoS 4 -LDH catalyst was found more efficient as clear from the observed atrazine (ATZ) degradation rate of 0.117 min −1 , 100 times higher than the Fe 3+ /PMS or 25–50 times higher than the Fe based single centre NO 3 -LDH/PMS, CO 3 -LDH/PMS or S 2 O 4 -LDH/PMS systems, respectively. This boosted efficiency was related to the electron-rich MoS 4 2− centre which allows the constant electron transfer to reduce the electron-deficient Fe 3+ center at MoS 4 -LDH surface and thereby accelerating the Fe 2+ /Fe 3+ redox cycle during reaction. Furthermore, the MoS 4 -LDH/PMS system exhibited a broader effective pH (3.0–9.0), good stability and minimum influence of background electrolyte or organic matter. The degradation pathway of ATZ based on free radical (SO 4 – and OH), involving the redox cycles of Fe 3+ /Fe 2+ and Mo 6+ /Mo 4+ was proposed for the activation of PMS . This work highlighted the essential role of MoS 4 2− moiety, to accelerate the Fe 3+ reduction at the surface of the LDH catalyst through the continuous feeding of electrons.

CAS / MDL: 3317-61-1
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2019 · IF 2.931

Tunable photoluminescence studies based on blue-emissive carbon dots and sequential determination of Fe(III) and pyrophosphate ions

Aiwen Yu,Yiping Tang,Kai Li,Jinwei Gao,Yuhui Zheng,Zhi Zeng

Fluorescence has been well documented and the optical feature of carbon dots generates considerable interests. Here the nitrogen-doped carbon dots with a relative quantum yield of 25% have been prepared. It displays stable blue emission based on the excitation at 355 nm. The carbon nanomaterial is highly dispersible in aqueous solution and can be employed as an effective optical probe for label-free detection of Fe 3+ (0.87 μM) via a switched off change. Additionally, such sensing nanoplatform can be recovered in the presence of pyrophosphate (PPi) and an “off-on” process has been identified. It is expected that this on-off-on strategy will allow new possibilities for developing efficient sensors in industrial fields.

CAS / MDL: 3458-72-8
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