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CATALYSIS TODAY · 2022 · IF 6.562

Improved olefin selectivity during CO hydrogenation on hydrophilic Fe/HAP catalysts

Xinyu Guo,Bo Liu,Xinhua Gao,Fugui He,Qingxiang Ma,Subing Fan,Tian-sheng Zhao,Jumei Tian,Prasert Reubroycharoen,Jianli Zhang

The hydrophilic/hydrophobic properties of catalysts greatly influence product distribution by tuning the secondary reactions during Fischer–Tropsch synthesis. Studies have confirmed that hydrophilic modification can inhibit secondary reactions. Herein, hydroxyapatite (HAP)-supported Fe catalysts (Fe/HAP) were prepared using an impregnation method. The effect of the catalyst surface properties on the product distribution in CO hydrogenation was studied. The surface hydroxyl groups on Fe/HAP promoted the growth of carbon chains and improved olefin selectivity. The addition of Na as a promoter to Fe/HAP suppressed the formation of undesirable CH 4 , further improving the selectivity for light olefins and C 5 + hydrocarbons. Compared with Fe 2 O 3 , Fe/HAP showed lower CH 4 selectivity (15%) and higher C 5 + selectivity (45%). Meanwhile, the Fe/HAP -Na catalysts with a higher selectivity of light olefins (with an O/P ratio reaching 4.51).

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JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY · 2022 ·Vol. 103 ·期 2 ·505-514 · IF 2.606

Macroporous Ni-Fe hydroxide bifunctional catalyst for efficient alkaline water splitting

Zou Chang,Guo Xingzhong,Wang Fan,Tian Rui,Hou Yang,Liu Fu,Yang Hui

Three-dimensional macroporous heterostructural Ni-Fe hydroxides with different mole ratio (Ni x Fe (1−x) -PH) were prepared via a sol-gel process combined with phase separation, and the overall water splitting electrocatalytic activity of the resultant macroporous Ni-Fe hydroxides were investigated in detail. The as-prepared Ni-Fe hydroxide has cocontinuous skeletons and interconnected macropores with a narrow pore size distribution (~150 nm), and possesses outstanding electrocatalytic activity with an overpotential of 263 mV for oxygen evolution reaction (OER) and 175 mV for hydrogen evolution reaction (HER) at 10 mA·cm −2 in 1 M KOH, respectively. The Ni 0.6 Fe 0.4 -PH | | Ni 0.6 Fe 0.4 -PH has efficient overall water splitting performance with a cell voltage of 1.61 V at 10 mA·cm −2 and great stability. The fantastic macropore structure and strong synergistic effect between Ni-Fe hydroxides significantly reinforce the contact area between the electrocatalyst and electrolyte, and endow high electrocatalytic performance of bifunctional electrocatalysts. The epoxide-induced sol-gel process accompanied by phase separation allows the synthesis of macroporous heterostructural Ni-Fe hydroxide bifunctional catalyst with a mass of active sites, displaying excellent electrocatalytic activity and low overpotential at several current densities for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER).

CAS / MDL: 7758-94-3 7791-20-0
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JOURNAL OF SOLID STATE CHEMISTRY · 2022 · IF 3.656

Cu-doped MIL-101(Fe) with enhanced photocatalytic nitrogen fixation performance

Zhipeng Zhang,Feifei Li,Guoqiang Li,Rui Li,Yunfang Wang,Yawen Wang,Xiaochao Zhang,Lulu Zhang,Fangfang Li,Jianxin Liu,Caimei Fan

The bottlenecks of photocatalytic nitrogen fixation are adsorption and activation of nitrogen, because N–N bond in dinitrogen is one of the strongest bonds in chemistry . Herein, for the first time, Cu-doped MIL-101(Fe) was applications in photocatalytic nitrogen fixation. The photocatalytic nitrogen fixation activity of Cu-MIL-101(Fe) is three times that of MIL-101(Fe). Characteristic of MIL-101(Fe) and Cu-MIL-101(Fe) are systematically compared by XRD , SEM, TEM, BET, PL and energy band structure . These results indicated that the Cu doping not only enlarge the specific surface area from 1413 ​m 2 /g to 2097 ​m 2 /g, but also increase the photoreduction capability from −0.13 ​V to −0.7 ​V. These results indicated that nitrogen adsorption and activation capacity can be improved by Cu doping. By combining metal ions doping and components regulation of MOFs , this work provides many future opportunities for enhance photocatalytic nitrogen fixation activity.

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KOREAN JOURNAL OF CHEMICAL ENGINEERING · 2022 ·Vol. 39 ·期 10 ·2685-2690 · IF 3.146

Degradation of sulphapyridine by Fe-Mn binary oxide-mediated radical reactions

Wu Kang,Zhang Zhongliang,Hua Fei,Ye Zhou,Li Chao,Yao Youzhi

Sewage containing antibiotics is harmful to the water environment. Here, a newly prepared iron manganese binary oxide (FMBO) activated persulfate (PDS) has excellent performance for the degradation of sulfapyridine (SPY) in an aqueous environment. The effects of initial pH, SPY, PDS concentration and FMBO dosage on the degradation ability of SPY were investigated. When the pH of FMBO/PDS was 4.0 and the initial concentration of PDS was 2.0 mmol/L, the degradation ratio of SPY could reach 94.4%. In the system of removing organic pollutants by transition metal activated PDS, SO −• 4 and •OH radicals are generally generated, and •OH radical plays a major role. Through the identification of SPY intermediate products by LC/MS, the degradation mechanism was explored. The degradation pathway showed that the strong oxidation of FMBO and the activity of PDS promoted the production of hydroxyl radical and contributed to the degradation and transformation of antibiotics. This study shows that FMBO/PDS has high degradation efficiency in the degradation of SPY.

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JOURNAL OF CATALYSIS · 2022 · IF 8.047

Regulating iron species compositions by Fe-Al interaction in CO2 hydrogenation

Minjie Xu,Xianglin Liu,Guiyao Song,Yingying Cai,Bianfang Shi,Yitao Liu,Xiaoxu Ding,Zixu Yang,Pengfei Tian,Chenxi Cao,Jing Xu

Different iron species exhibit distinct activity and selectivity in CO 2 hydrogenation reaction. Herein, by controlling calcination temperature, Fe-Al interaction in Na promoted Fe-Al catalysts has been regulated, which further leads to various compositions of iron oxide (FeO x ) and iron carbides (Fe 7 C 3 and Fe 5 C 2 ) after CO activation and CO 2 hydrogenation reaction. The phase compositions and structures of Fe-Al catalysts are carefully distinguished by multiple characterizations, including XRD, XPS, MES and TEM, and the reactivity of different phases is studied with the combination of experiments (kinetics, TP and in situ DRIFTS) and Density Functional Theory (DFT) calculations. Our FeAl350 with the highest FeC x content shows the highest CO 2 conversion of 48.2% and the lowest CO selectivity of 10.1%, and FeAl900 with the highest Fe 5 C 2 / FeC x ratio presents the highest C 5+ selectivity of 44.6%. Finally, a correlation between different compositions of iron species with the activity and selectivity of Fe-based for CO 2 hydrogenation to olefins was established.

CAS / MDL: 7784-27-2 7782-61-8
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METALLURGICAL AND MATERIALS TRANSACTIONS B-PROCESS METALLURGY AND MATERIALS PROCESSING SCIENCE · 2022 ·Vol. 53 ·期 4 ·2634-2646 · IF 2.872

Separation of Zn and Fe in ZnFe2O4 by Reaction With MgCl2

Huang Jingdong,Sohn Il,Kang Youngjo,Yang Xiao

Earth’s commercial and affordable zinc reserves are expected to be depleted in less than 50 years. Since electric arc furnace (EAF) dust contains a certain amount of Zn, recovery of Zn from EAF dust has become an important issue to assure a sustainable resource supply in the future. The key technical challenge is that Zn mainly occurs in EAF dust as ZnFe 2 O 4 , a very stable crystal which is difficult to reduce or leach. MgCl 2 is believed to be effective in breaking the structure of ZnFe 2 O 4 . This work investigates the fundamentals of the reaction between MgCl 2 and ZnFe 2 O 4 . Experiments show that Zn in ZnFe 2 O 4 is chlorinated to ZnCl 2 quickly with priority over Fe, implying the efficacy of MgCl 2 in separating Zn and Fe in ZnFe 2 O 4 by selective chlorination. Effects of MgCl 2 /ZnFe 2 O 4 molar ratio and temperature on the reaction are clarified. Overuse of MgCl 2 slows down the reaction and is detrimental to the selective chlorination of Zn. Temperature can effectively increase the reaction rate as well as the priority of chlorinating Zn. Utilization of MgCl 2 could be high, because evaporation of MgCl 2 is not as fast as the reaction with ZnFe 2 O 4 . According to these results, a new technology to recover Zn from EAF dust by using MgCl 2 is proposed.

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ACS Applied Nano Materials · 2022 · IF 6.14

Fe Single-Atom Electrochemical Sensors for H2O2 Produced by Living Cells

Yi Liang,Peng Zhao,Jilin Zheng,Yuanyuan Chen,Yiyi Liu,Jia Zheng,Xiaogang Luo,Danqun Huo,Changjun Hou

Reasonable sensor construction for precisely real-time detecting H2O2 produced from living cells has always been of great significance and challenges. Due to the excellent catalytic efficiency and unparalleled peroxidase-like activity, single-atomic catalysts with Fe-Nx active sites show great potential in H2O2 detection. These special atomic active sites make it easier for the Fenton reaction to occur, which provides basic support for H2O2 sensors. Their application in the in situ real-time detection of H2O2 has important market prospects. Herein, single-atomic Fe catalysts with distorted graphitic carbon are obtained through a simpler preparation method. A precursor hemin@zeolitic imidazolate framework-8 (hemin@ZIF-8) is calcined at a high temperature and carbonized to get the nitrogen-carbon codoped Fe single atoms (Fe SAs-N/C) and then successfully prepare a H2O2 electrochemical sensor by modifying it on a glassy carbon electrode (GCE). Its peroxidase activity is calculated by enzymatic kinetics, which shows a better peroxidase activity compared with horseradish peroxidase and other reported single-atom (SA) materials. Moreover, the electrocatalytic kinetics is explained by Laviron calculation, which more directly confirms that it has a faster electron transfer rate. Importantly, Fe SAs-N/C@GCE has a wider linear range than sensors combined with other SA materials and a low detection limit of 0.34 μM. It is an attractive design of H2O2 sensors and single-atomic catalysts with superior substrate affinity that are novel alternatives to natural enzymes.

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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2021 · IF 8.067

Improved electromagnetic dissipation of Fe doping LaCoO3 toward broadband microwave absorption

Fan Wang,Weihua Gu,Jiabin Chen,Qianqian Huang,Mingyang Han,Gehuan Wang,Guangbin Ji

Perovskite LaCoO 3 is of great potential in electromagnetic wave absorption considering its outstanding dielectric loss as well as the existing magnetic response with the magnetic doping. However, the dissipation mechanism of the magnetic doping on the microwave absorption is lack of sufficient investigated. In this paper, LaCo 1- x Fe x O 3 ( x =0, 0.05, 0.1, 0.15, 0.2, 0.25, 0.3, LCFOs) perovskites with different Fe doping amounts were prepared successfully by the sol-gel method and subsequent heat treatment in the air atmosphere. The structure characterization carried out by the first-principles calculations shows the effect of Fe doping on the dielectric and magnetic properties of LCFOs and the strong hybridization of Co/Fe-3d with O-2p in the LCFOs system was successfully demonstrated. Particularly, when x =0.1 and the thickness is only 1.95 mm, the LaCo 0.9 Fe 0.1 O 3 exhibits the best microwave absorption performance with the minimum reflection loss (RL) value of about -41 dB. The typical samples achieve a broad effective absorption bandwidth (EAB) of 5.16 GHz (7.92-13.08 GHz), which covers the total X band (8-12 GHz). Considering that, the especial Fe doping perovskite is promising to be a candidate as efficient microwave absorbers.

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ENERGY · 2021 · IF 7.147

Cellulose gasification with Ca–Fe oxygen carrier in chemical-looping process

Genyang Tang,Jing Gu,Zhen Huang,Haoran Yuan,Yong Chen

Biomass-derived chemical looping gasification (BCLG) is a novel technology for lignocellulose energy applications . Ca–Fe oxygen carriers have been proven to be a potential material for efficient lignocellulose conversion and hydrogen-enriched syngas production in process studies. In this study, Thermogravimetry-mass spectrometry (TG-MS), pyrolysis chromatography-mass spectrometry (Py-GC-MS) and fixed-bed experiments were conducted, and the cellulose BCLG product was analyzed to explore the mechanism of reaction between Ca–Fe OCs and biomass char or volatiles. The mechanism of the synergistic effect of Ca–Fe was analyzed to explain the characteristics of the OCs. The results suggest the Ca-based materials act as catalysts to promote the decomposition of cellulose monomers at primary reaction and char at secondary reaction, and also promote the reforming and oxidation of volatiles by chemisorption . Ca participates in the construction of inert substances, such as Ca 2 Fe 2 O 5 , to avoid the deep oxidation of CO and H 2 . Fe-based material supplies oxygen and promotes the reforming of volatile. Compared with Fe 2 O 3 and CaO/Fe 2 O 3 , CaFe 2 O 4 shows a better performance on carbon conversion and H 2 production below 850 °C.

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CLAY MINERALS · 2021 ·Vol. 56 ·期 2 ·99-107 · IF 1.478

Enhanced thermal stability and adsorption performance of MIL-53(Fe)@montmorillonite

Fengli Dai,Junhui Guo,Yufeng He,Pengfei Song,Rongmin Wang

Montmorillonite (Mnt), a clay mineral with a nanolayered structure, was combined with an Fe-based metal–organic framework (MOF; MIL-53(Fe)) using an in situ growth technique that yielded a novel eco-friendly clay-based adsorbent (MIL-53(Fe)@Mnt). The adsorbent was characterized by scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, thermogravimetric analysis and N2 gas adsorption. The MIL-53(Fe) particles grew on the surface of the nanolayered Mnt and the MIL-53(Fe) particle size became smaller. The adsorption performance of MIL-53(Fe)@Mnt was investigated by removing methylene blue (MB), and optimization experiments were carried out to study the effects of contact time, pH, initial dye concentration and adsorbent mass on the adsorption processes. The MIL-53(Fe)@Mnt exhibited excellent adsorption capacity for MB, namely 313.7 mg g−1, which was 3.02 times and 3.54 times greater than that of pure Mnt and MIL-53(Fe), respectively. Adsorption was fitted with the Langmuir isotherm model and followed a pseudo-second order kinetic model. The MIL-53(Fe)@Mnt obtained is a low-cost and eco-friendly adsorbing material and might be a candidate for removing dyes during water treatment.

CAS / MDL: 100-21-0
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Scientific Reports · 2021 ·Vol. 11 ·期 1 ·1-11 · IF 4.38

Removal of hexavalent chromium from wastewater by Cu/Fe bimetallic nanoparticles

Ye Jien,Wang Yi,Xu Qiao,Wu Hanxin,Tong Jianhao,Shi Jiyan

Passivation of nanoscale zerovalent iron hinders its efficiency in water treatment, and loading another catalytic metal has been found to improve the efficiency significantly. In this study, Cu/Fe bimetallic nanoparticles were prepared by liquid-phase chemical reduction for removal of hexavalent chromium (Cr(VI)) from wastewater. Synthesized bimetallic nanoparticles were characterized by transmission electron microscopy, Brunauer–Emmet–Teller isotherm, and X-ray diffraction. The results showed that Cu loading can significantly enhance the removal efficiency of Cr(VI) by 29.3% to 84.0%, and the optimal Cu loading rate was 3% (wt%). The removal efficiency decreased with increasing initial pH and Cr(VI) concentration. The removal of Cr(VI) was better fitted by pseudo-second-order model than pseudo-first-order model. Thermodynamic analysis revealed that the Cr(VI) removal was spontaneous and endothermic, and the increase of reaction temperature facilitated the process. X-ray photoelectron spectroscopy (XPS) analysis indicated that Cr(VI) was completely reduced to Cr(III) and precipitated on the particle surface as hydroxylated Cr(OH) 3 and Cr x Fe 1−x (OH) 3 coprecipitation. Our work could be beneficial for the application of iron-based nanomaterials in remediation of wastewater.

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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2020 · IF 3.99

Novel fluorescent hydrogel for the adsorption and detection of Fe (III)

Dongdong Zhang,Xuetao Tian,Huanhuan Li,Yiping Zhao,Li Chen

A novel PNIPAAm-CD hydrogel with good adsorption property and stable fluorescence detection for Fe 3+ was prepared by copolymerizing PCDs with NIPAAm monomers. As a fluorescence probe, carbon quantum dots (CDs) were modified by glycidyl methacrylate (GMA) to obtain PCDs, which had double bond and could react with N-isopropyl acrylamide to form hydrogel. The functionalization of the amine groups on the surface of the PCDs enables PNIPAAm-CD hydrogel also exhibits photoluminescence behavior. In addition, the PNIPAAm-CD hydrogels stably shows higher adsorption performance for Fe 3+ than the pure PNIPAAm hydrogel. The honeycomb PNIPAAm-CD hydrogel had a good quenching response to metallic iron ions, and the detection limit was as low as 0.27 μM in the range of 1μM~1mM. The results of adsorption isotherms and adsorption kinetics showed that the adsorption procedure of metal ions conforms to the pseudo-second-order model and langmuir model, respectively. The effective detection and the high adsorption of PNIPAAm-CD hydrogel for Fe 3+ make it an effective portable platform potential, which has the dual functions of visual detection and adsorption of Fe 3+ .

CAS / MDL: 6119-70-6
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