CHEMOSPHERE
·
2020
·
IF 5.778
Zhiyong Zhang,Yi-bo Hu,Wenjuan Ruan,Huiying Ai,Baoling Yuan,Ming-Lai Fu
2,4-dichlorophenol (2,4-DCP) is a typical chlorophenol that has been widely used in industrial production and caused serious pollution to the environment. In this study, the performance of Fe/Ni bimetallic nanoparticles supported on polystyrene cation exchange resin (Fe/Ni-D072) to remove 2,4-DCP was evaluated. The effects including the doping amount of Ni, the dosage of Fe/Ni-DCP, the initial concentration of 2,4-DCP, and pH value of the solution on the removal efficiency were also investigated. The results showed that when the initial concentration of 2,4-DCP was 20 mg/L and pH = 7.3, 90% of 2,4-DCP could be dechlorinated by Fe/Ni-D072 (Ni% = 30 wt%, dosage: 6.7 g/L) after 12 h reaction. The dechlorination process followed a pseudo-first-order model, and the reaction constant was 0.252 h −1 . In addition, the effects of humic acid and common coexisting ions on dechlorination were studied. The results showed that humic acid with a low concentration (5 mg/L) and CO 3 2− restrained the degradation of 2,4-DCP. The dechlorination products of 2,4-DCP were identified by HPLC and the result showed phenol was the main product with a slight amount of 2-CP as the dechlorination intermediate, and 4-CP was barely detected. These results suggest that Fe/Ni-D072 was a promising catalytic material for the removal of chlorophenol and has great application prospects in groundwater remediation .
研究领域:
环境科学
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材料科学
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产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Shumin Li,Jun Tan,Zhejun Jiang,Jin Wang,Zhengquan Li
Dye-sensitized systems show promising in photocatalysis because they can separate the tasks of light absorption, charge generation and surface catalysis to two coupled components. In this system, it is crucial to develop suitable catalysts capable of receiving dye-injected charges and having high activity to a given reaction. Aiming to photocatalytic H 2 and O 2 production, we present a metal-organic framework derived route to prepare bimetallic Fe-Ni-P nanotubes using Fe-Ni-MIL-88 nanorods as templates. When integrated with different dyes, these Fe-Ni-P nanotubes can serve as efficient catalysts for photocatalytic H 2 and O 2 production, respectively. Additionally, catalytic activities of such dye-sensitized systems can be conveniently regulated by tailoring the metal compositions in Fe-Ni-P nanotubes. The photocatalytic H 2 production of Fe 1 -Ni 2 -P can reach 5420 μmol g cat −1 h −1 under eosin-Y sensitization, which is 24 times and 6.7 times higher than Fe 2 P and Ni 2 P, respectively. The photocatalytic O 2 production of Fe 1 -Ni 2 -P can reach 900.3 μmol g cat −1 h −1 under [Ru(bpy) 3 ]Cl 2 sensitization, about 4.6 times and 2.9 times higher than Fe 2 P and Ni 2 P. The roles of different components in the system have been explored and corresponding working mechanism is proposed. This work demonstrates a new type of dye-sensitized systems consisting of bimetallic phosphides and provides a facile route to regulate their photocatalytic performance.
研究领域:
材料科学
·
光催化
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DOI
高影响因子
ACS Catalysis
·
2021
·
IF 13.084
Ting Wang,Yuebing Xu,Yufeng Li,Lei Xin,Bing Liu,Feng Jiang,Xiaohao Liu
Conversion of syngas into aromatics via the Fischer–Tropsch (FT) route provides a promising way to supply the value-added chemicals. However, it is still a great challenge to achieve controllable aromatics selectivity with good stability. Herein, we report the Na-mediated bimetallic Fe–Ni catalyst simply particle mixed with HZSM-5, which can boost the stable and selective production of aromatics from the syngas. In detail, FeNiOx(5:1)-0.41Na exhibits quite stable catalytic activity with notably higher selectivity to light α-olefins (C2=–C4=) compared to α-Fe2O3-0.75Na. Various characterizations suggest that an appropriate addition of Ni with Na substantially regulates iron carbide formation and suppresses carbon deposition owing to the electron donation of Fe to Ni reducing CO adsorption and dissociation. Interestingly, extra Na results in remarkably increased selectivity to C1o–C4o, despite the fact that Na shows the ability to suppress hydrogenation. Both characterizations and density functional theory (DFT) calculations demonstrate that the addition of Na weakens the Fe–Ni interaction and reduces electron transfer from Fe to Ni, which promotes C1o–C4o formation as Ni tends to reflect its intrinsic catalysis. DFT calculations confirm that the adsorbed CH2 species at the Ni–Fe interface prefers to undergo coupling to form C2H4, and the formed C2H4 spontaneously desorbs from the surface, indicating that the formation of lower olefins is favorable and further chain growth is inhibited. This could be attributed to the fact that the accumulated electron at the Ni–Fe interface weakens the binding strength of CH2 and C2H4 species because of electronic repulsion. Furthermore, the effects of FT product distribution on aromatics formation were also investigated. FeMnOx(5:1)-0.40Na produces longer olefin-rich hydrocarbons in C5+ owing to oxygen vacancy-assisted CO dissociation, leading to highly branched monocyclic aromatics and faster HZSM-5 deactivation because of increased coking from the isomerization–hydrocracking of long hydrocarbons. In contrast, FeNiOx(5:1)-0.41Na-HZSM-5 produces major light aromatics about 65.7% including toluene, ethyl-benzene, and xylene in total aromatics with about 98.6% aromatics in the liquid phase, which benefits from the fact that FeNiOx(5:1)-0.41Na makes shorter hydrocarbons in C5+ and/or Ni metal has a strong ability of H2 dissociation to provide atomic H spillover onto HZSM-5. Thus, HZSM-5 also shows improved stability. Note that the mixed catalysts with a high Na content indicate a substantial Na+ migration to increase light α-olefins in the gas phase owing to suppress H-transfer reaction. This study provides deep insights into how to develop stable and selective iron-based catalysts for the production of FT products and its further conversion into value-added light aromatics.
研究领域:
催化化学
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材料科学
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能源化学
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产品关联
DOI
高影响因子
Catalysis Science & Technology
·
2021
·Vol. 11
·期 24
·7943-7954
·
IF 6.119
Hao Zhang,Xiaojing Song,Hao Sun,Zhenyu Lei,Shouxin Bao,Chen Zhao,Dianwen Hu,Wenxiang Zhang,Jingyao Liu,Mingjun Jia
Developing highly efficient and durable eco-friendly heterogeneous catalysts for the Friedel–Crafts acylation (FCA) reaction has been a long-term and significant target, yet remains a great challenge. Herein, a series of Fe–Ni alloy nanoparticles (NPs) encapsulated inside N-doped carbon spheres (FexNi1−x@NC) was rationally fabricated by pyrolyzing the Fe–Ni bimetallic metal–organic frameworks (BMOFs-FexNi1−x) to this end. Various characterization results demonstrated that FeNi alloy NPs (25 nm) covered by a thin carbon shell (5 nm) were uniformly distributed throughout the entire carbon-based composite. A number of oxidized metal species (Fe3+, Ni2+) are present on the surface of the inner bimetallic core, which should be the main source of catalytically active centers of the carbon-wrapped metal NP catalysts. The composition-optimized Fe0.8Ni0.2@NC with relatively higher positive surface charges exhibited the highest catalytic activity and excellent stability for the acylation of aromatic compounds with acyl chlorides. The density functional theory calculations revealed that the catalytic activity of the FexNi1−x@NC catalysts could arise from the electron transfer, i.e., from the outermost layer of the carbon shell to the inner positively charged Fe-based metal NPs, which can lead to a positive charge distribution (by acting as weak Lewis acid sites) on the external surface of the carbon-encapsulated metal NP catalysts. In this case, the external carbon shell can function as ‘chainmail’ to transfer the Lewis acidity (positive charge), and also to protect the inner metal core from the destructive reaction environment, thus resulting in the formation of highly efficient and durable FCA catalysts.
研究领域:
材料科学
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催化化学
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绿色化学
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Qiwen Pan,Fei Lin,Ruiqi Liu,Yilin Li,Xinyue Zhang,Rui Luo,Lingling Cai,Yang Liu,Wuguo Deng,Liru He
Nanocatalysts provide a platform for developing anti-tumor strategies by activating intratumoral chemical catalysis to produce highly toxic reactive oxygen species (ROS). However, the biological effect of nanocatalysts on tumor cells, which is pivotal for effective nanotherapy treatment, remains poorly understood. Herein, we present a general and facile method of synthesizing Fe/Ni-layered double hydroxides (LDHs) for enhanced apoptosis- and ferroptosis-induced cancer nano-therapy, as well as a potential mechanism underlying the anti-tumor effect based on transcriptome sequencing. An analysis of the chemical structure suggests that the Fe atoms interact strongly with the Ni atoms in Fe/Ni-LDH. Compared with Fe-OH and Ni-OH, Fe/Ni-LDH exhibited significantly better ROS-catalytic activity, with a V max of 5.015 × 10 −2 μM·s −1 , and generated massive amounts of •OH and O 2 •− radicals, enabling outstanding chemo-dynamic therapy. Both in vitro and in vivo experiments indicated a robust apoptosis-induced cell death pathway, increased intracellular oxidative stress, and accumulation of lipid peroxide (LPO), promoting ferroptosis-involved cancer-cell death, which was further confirmed by transcriptome sequencing. The Fe/Ni-LDH biocatalyst not only provides a robust nanoplatform for tumor suppression but also encourages further exploration and applications of nanobiocatalysts.
研究领域:
生物医学工程
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肿瘤学
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纳米医学
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产品关联
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2023
·
IF 6.6
Zhiwen Xu,Guangyu Chen,Fei Yang,Juhee Jang,Guimei Liu,Fei Xiao,Yan Sun,Xiaoyi Qiu,Weiwei Chen,Dong Su,Meng Gu,Minhua Shao
The development of inexpensive and high-performance bifunctional electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is of crucial significance for rechargeable metal-air batteries , but remains challenging. Herein, we report an ingenious bifunctional oxygen electrocatalyst integrating ZIF-derived carbon-anchored Fe/Ni single atoms, FeNi alloy nanoparticles , and graphene support (denoted as Fe/Ni-NC||FeNi@G). Synergizing highly active Fe single atoms for the ORR and highly efficient FeNi alloy nanoparticles for the OER, the as-constructed Fe/Ni-NC||FeNi@G catalyst exhibits outstanding bifunctionality; the potential gap between the OER potential at 10 mA cm –2 and the ORR half-wave potential is only 0.618 V, outperforming the benchmark Pt/C + Ir/C catalyst and most transition metal-based bifunctional catalysts reported in the literature. More importantly, the Fe/Ni-NC||FeNi@G-driven zinc-air battery (ZAB) delivers a maximum power density of ∼200 mW cm –2 , a specific capacity of 876 mAh g –1 , and excellent cycling stability with negligible voltage decay up to 500 hours (3000 cycles). This work provides an effective approach to designing highly efficient non-noble metal multifunctional catalysts for practical applications in rechargeable metal-air batteries.
研究领域:
材料科学
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电化学
·
能源存储
·
催化
✓ 已验证
产品关联
DOI
高影响因子
JOM
·
2024
·
IF 2.1
Yu Yu,Li Ying,Zhong Yiwei,Wang Mingyong,Guo Zhancheng
Fe-Ni-Co alloy films demonstrate outstanding soft magnetic properties and are widely used as magnetic materials. The ultrasonic-assisted electrodeposition method is highly regarded for its merits in improving alloy film performance. In this study, Fe-Ni-Co alloy film with a uniform composition was fabricated through ultrasonic-assisted electrodeposition. The effects of the electrodeposition parameters on the composition and microstructure of the Fe-Ni-Co alloy films were studied. The results revealed that lower initial electrolyte pH, temperature ( T ), and ultrasonic power ( P ) were conducive to the increase of the iron content of the alloy films. As the ultrasonic power increased, the crystal structure of the Fe-Co-Ni films changed from bcc (FeCo) to fcc (NiFe), and the mean grain size decreased. When the electrodeposited condition was pH = 2, T = 50°C, and P = 45 W, the Fe 58.36 Ni 36.01 Co 5.63 alloy film showed a better corrosion resistance than 304 stainless steels. When the electrodeposited condition was pH = 2, T = 50°C, and P = 90 W, the Fe 53.84 Ni 41.66 Co 4.48 alloy film exhibited good magnetic properties, and the saturation magnetic induction and coercivity were 1.75 T and 85 A/m, respectively, which was much better than Fe-Co-Ni alloy films (Ni: about 40 wt.%) prepared by traditional electrodeposition.
研究领域:
材料科学
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电化学
·
冶金学
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产品关联
DOI
高影响因子
JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS
·
2024
·
IF 2.5
Zhangqiao Zhou,Qi Li,Meiqi Wen,Ruilin Zhou,Xian Wang
The coatings play a crucial role in enhancing the performance of soft magnetic composites (SMCs). This study aims to create coatings for Fe-Ni-Mo SMCs using polysilazane (PSZ) as the precursor. The transformation mechanism of the PSZ/resin mixture is studied by analyzing functional groups and chemical bonds at various temperatures. During the self-polymerization process of PSZ at 350 °C, N–H, C = C–H, Si-H bonds, –CH 3 , and Si-CH 3 groups undergo crosslinking reactions to form C–C and Si-N bonds. When the temperature reaches 600 °C, PSZ polymer cleavage, O-Si-C and Si-N-Si bond dominate in the coating. Additionally, PSZ can effectively enhance the heat resistance of silicone resin through its reaction with Si-OH groups, which has a significant effect on increasing the resistivity of SMCs and reducing high frequency core loss. Optimizing the PSZ content to 0.5 wt% enhances the magnetic properties of Fe-Ni-Mo SMCs, resulting in a μ e of 74.0 at 100 kHz and a corresponding core loss ( P cv ) of 547.7 mW/cm 3 at 100 kHz/100 mT. The findings provide valuable insights for optimizing PSZ content to improve magnetic performance in SMCs.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
Catalysis Science & Technology
·
2019
·Vol. 9
·期 9
·2282-2290
·
IF 5.726
Dawei Zhou,Peixue Wang,Yan Long,Yuqing Fei,Youquan Deng
The thermal cracking behavior of diethyl hexamethylenedicarbamate (EHDC) was investigated in this work. The polymers formed under different conditions were analyzed by IR and TG, indicating that the polymers were mixtures of EHDC, polyureas, imines and others. The polymers could be converted to EHDC by a simple alcoholysis reaction for the first time over Fe–Ni/Al2O3 catalysts. Under the optimized reaction conditions, the yield of EHDC could reach up to 52% with 99% selectivity over 8% Fe–3% Ni/Al2O3 catalysts. The catalysts were extensively characterized by BET, XPS, XRD, SEM, TEM, H2-TPR and NH3-TPD, showing that the interaction effect between Fe species and Ni species may be attributed to high catalytic performance of the catalyst. Meanwhile, the loss of active components resulted in decreased catalytic activity.
研究领域:
化学工程
·
催化科学
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产品关联
DOI
高影响因子
Materials Research Express
·
2017
·Vol. 4
·期 8
·085009
·
IF 1.068
Zongtang Liu,Chenggang Gu,Yongrong Bian,Xin Jiang,Yufeng Sun,Zhenghao Fei,Jingtao Dai
In this study, Fe/Ni bimetallic nanoparticles were supported on the attapulgite (A-Fe/Ni) to enhance the degradation reactivity of decabrominated diphenyl ether (BDE209) in aqueous solution. The Fe/Ni nanoparticles were well distributed on the attapulgite surface with an average diameter of 20–40 nm. The removal percentage of BDE209 by A-Fe/Ni was 1.59 times higher than Fe/Ni nanoparticles alone because attapulgite could act as supporting material to disperse Fe/Ni nanoparticles and prevent Fe/Ni nanoparticles from aggregation. The degradation kinetics for BDE209 debromination by A-Fe/Ni could be well described by a pseudo-first-order model, and the debromination rate constant of BDE209 increased with increasing the dosage of A-Fe/Ni, water/THF ratio, and decreasing the initial BDE209 concentration and solution pH. The degradation products were identified using a third-order polynomial regression equation between the experimental and reference gas chromatography relative retention times. Stepwise debromination from n-bromo-DE to (n − 1)-bromo-DE was a possible pathway with bromines being substituted sequentially by hydrogen. The preferred elimination of bromines of BDE209 by A-Fe/Ni followed the debromination preference of para-Br > meta-Br > ortho-Br. The results provide evidences for understanding the debromination mechanism of polybrominated diphenyl ether by clay-supported Fe/Ni nanoparticles.
研究领域:
环境科学
·
化学工程
✓ 已验证
DOI
高影响因子
ANALYST
·
2020
·Vol. 145
·期 19
·6349-6356
·
IF 3.978
Ye Hu,Chaochao Yue,Jing Wang,Yuhua Zhang,Wenhui Fang,Jiaqi Dang,Ying Wu,Hong Zhao,Zengxi Li
Fe–Ni-MOFs with different amounts of Fe are synthesized through a two-step template etching method. Kinetic analysis indicates that Fe–Ni-MOF exhibits prominent intrinsic peroxidase-like activity, which could catalytically oxidize 3,3′,5,5′-tetramethylbenzidine (TMB) to produce oxidized TMB (oxTMB) with a blue color. As a peroxidase-mimicking MOF, Fe–Ni-MOF with its efficient stable catalysis properties is demonstrated to allow a sensitive colorimetric assay for Sn2+ ions. The mechanism is explored, whereby Sn2+ ions could reduce the peroxidase-like activity of Fe–Ni-MOF based on a redox interaction, making the oxTMB color lighter and decreasing the absorbance intensity at 652 nm. The linear determination of the Sn2+ ion concentration using a UV-vis spectrometer ranges from 0.01 mM to 1.0 mM and from 1.0 mM to 4.0 mM. The presented Fe–Ni-MOF-based assay of Sn2+ ions was successfully applied to real water samples.
研究领域:
材料科学
·
分析化学
·
环境科学
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF ENVIRONMENTAL MANAGEMENT
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2022
·
IF 8.91
Fang Guo,Yaoyin Lou,Qun Yan,Jianglei Xiong,Jiahao Luo,Chikang Shen,Dimitris V. Vayenas
For the efficient removal of the bio-refractory organic pollutants in the electronic industry wastewater, the Ni–Fe (oxides) modified three-dimension (3D) particle electrode was applied in electro-Fenton system (3D/EF), where iron ions were released from anode and deposited onto algal biochar (ABC) to prepare composite catalyst during reaction process. Firstly, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) analysis were applied to confirm successful fabrication of the 3D particle electrode materials . Secondly, COD removal efficiency could reach about 80%, which was about 20% higher than that in 2D/EF system, under the optimized conditions as 2.0 g/L of Ni-ABC particle electrodes, initial pH of 3, 100 mL/min of aeration intensity and 20 mA/cm 2 of applied current density. Thirdly, characterized using three-dimensional fluorescence spectroscopy and GC-MS analysis, it seemed that most of the macromolecular substances could be degraded, whereas mono-2-ethylhexyl phthalate (MEHP) was identified as the most abundant and representative compound. Finally, possible degradation pathway of MEHP in 3D/EF system was proposed including dealkylation, cleavage of C–O bond, and demethylation. Therefore, this study provides a new strategy in designing EF system employing bimetal doped biochar composite for an efficient elimination of organic pollutants within electronic industry wastewater.
研究领域:
环境科学
·
废水处理技术
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）