JOURNAL OF HAZARDOUS MATERIALS
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2020
·
IF 9.038
Qi Yang,Dan Chen,Libing Chu,Jianlong Wang
In present work, we studied a novel Fe/C nanomaterial fabricated using Fe-based metal organic frameworks (MOFs) as precursors through thermal pyrolysis to catalyze gamma irradiation-induced degradation of antibiotics, cephalosporin C (CEP-C) and sulfamethazine (SMT) in aqueous solution. The MOFs-derived Fe/C nanomaterials (DMOFs) had the regular octahedrons structure of MOFs and contained element C, Fe and O, while Fe° with a fraction of Fe 3 O 4 and Fe 2 O 3 were identified. Results showed that DMOFs addition could accelerate the generation of OH during gamma irradiation, while the intermediates of bonds cleavages of antibiotic molecules and OH addition were identified. DMOFs were more effective to improve the decomposition of antibiotic having the higher adsorption capacity like SMT. The degradation rate of CEP-C and SMT increased by 1.3 times and 1.8 times, and TOC reduction at 1.0 kGy reached 42 % and 51 %, respectively by gamma/DMOFs treatment, while only 20.2 % (CEP-C) and 4.5 % (SMT) of TOC reduction were obtained by γ-irradiation alone. The crystal structure, functional groups and magnetism of DMOFs changed slightly after gamma irradiation, which made it possible to be reused. DMOFs were promising to enhance the degradation of antibiotics during gamma irradiation.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Yunqi Wang,Peng Zhou,Qingguo Wang,Xiaowei Huo,Xue Huang,Qian Ye,Hao Xu,Guanyu Zhou,Yuhang Liu,Jing Zhang
Hydroxylated fullerene, Fullerol, has applied in many areas because of its high electron affinity and antioxidant potential, while it was few used in wastewater treatment. In this study, the mechanism involved that Fullerol accelerated the regeneration of Fe(II) in the Fe(III)/H 2 O 2 system under dark condition, which was investigated with chloramphenicol (CAP) as a model pollutant. In Fullerol/Fe(III)/H 2 O 2 system, CAP removal was completely achieved at 60 min via a non-photochemical pathway. In addition, the quenching experiments and electron spin resonance (ESR) results indicated that hydroxyl radical ( OH) was the main reactive oxygen species (ROSs). The Fullerol/Fe(III)/H 2 O 2 system had a rate constant of CAP degradation about 5.0 × 10 −2 min −1 , which was about 22 times higher than it in Fe(III)/H 2 O 2 Fenton-like system (2.3 × 10 −3 min −1 ). Fe(II) was ascertained the effective component that was responsible for H 2 O 2 activation to produce OH, which derived from 1) the first pathway: Fullerol complexed with Fe(III) and the redox potential of the complex is much lower than Fe(III)/Fe(II); 2) the second pathway: Fullerol acted as an electron donor to reduce Fe(III) into Fe(II). Moreover, CAP degradation intermediates were identified and its degradation pathways were proposed. This study suggested a new approach for improving the Fe(III)/H 2 O 2 system by accelerating Fe(III)/Fe(II) cycles with Fullerol.
研究领域:
环境科学
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废水处理
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
Nano-Micro Letters
·
2020
·Vol. 12
·期 1
·1-16
·
IF 12.264
Deng Baiwen,Xiang Zhen,Xiong Juan,Liu Zhicheng,Yu Lunzhou,Lu Wei
Sandwich-like laminated Fe&TiO 2 @C nanocomposites were successfully prepared from the MXene–MOFs hybrids.
A broad effective bandwidth of 6.5 GHz at a thickness of only 1.6 mm was achieved.
研究领域:
材料科学
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电磁学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Catalysis Science & Technology
·
2021
·Vol. 11
·期 8
·2864-2872
·
IF 6.119
Xiaoli Li,Yuan Tang,Yue Jiang,Manman Mu,Xiaohong Yin
A series of composites composed of Bi4O5Br2 and Fe-MIL were successfully fabricated for mimicking sunlight-driven photocatalytic reduction of CO2. Herein, Bi4O5Br2, as a modulator of solid acids, could turn NH2-MIL-101(Fe) into NH2-MIL-88B(Fe) completely at 0.07 wt% catalytic loading, where further addition could construct the corresponding composites of Bi4O5Br2 and NH2-MIL-88B(Fe). The highest activity in the photocatalytic reduction of CO2 was achieved at 7.96 μmol g−1 h−1 of CH4 at 3.28 wt% of Bi4O5Br2. Besides, this catalyst possessed high photostability during the recycling experiments and the mechanism of this process was thoroughly explored. This study provides a novel strategy employing solid acid modulators for regulating the structure and morphology of MOFs showing high activity and stability in the photocatalytic reduction of CO2 to CH4.
研究领域:
材料科学
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环境科学
·
化学
✓ 已验证
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2022
·
IF 9.965
Xiaolong Hu,Jingyu Bao,Daiwen Chen,Syed Jalil Shah,Sidra Subhan,Wenxue Gong,Wenyuan Li,Xinqi Luan,Zhongxing Zhao :,Zhenxia Zhao
In the photo-Fenton reactions, fast recombination of photoinduced electrons and holes in Fe-based metal–organic frameworks (Fe-MOFs) slows Fe(III)/Fe(II) cycle, which remains big challenge that significantly retards the overall process. Herein, NH 2 -MIL-88B(Fe) (NM88) was modified with 3,5-diaminobenzoic acid (DB) and TPB-DMTP-COF (COF-OMe) to in situ construct NM88(DB) 0.85 /COF-OMe composite that could strongly harvest the visible light for photo-Fenton degradation of sulfamerazine (SMR). With the addition of DB, electron-donating effect of NM88 was strengthened, which then promoted amino groups to react with aldehyde groups (Schiff-base), and thus highly facilitated the interfacial contact between NM88 and COF-OMe. Such modifications increased the degradation rate constants for NM88(DB) 0.85 /COF-OMe to 15.1 and 17.3 times that of NM88 and COF-OMe respectively with good reusability. Moreover, the catalyst exhibited 32–170 times higher degradation kinetics in comparison to other reported catalysts. Results showed that due to the Schiff-base reaction between NM88(DB) and COF-OMe, electron density on Fe(III) was decreased; and the photogenerated electrons of COF-OMe moved to NM88(DB) to reduce Fe(III), thus resulting in the generation of highly active Fe(II) and ·OH species. Furthermore, the main reactive species were determined to be ·OH and ·O 2 – by trapping experiments, and a possible mechanism of the degradation system followed Z-scheme charge transfer.
研究领域:
环境科学
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材料科学
✓ 已验证
DOI
PubMed
高影响因子
Sustainable Energy & Fuels
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2020
·Vol. 4
·期 5
·2192-2200
·
IF 5.503
Zhewen Ma,Qiuyu Zhang,Wen Zhu,Darvaish Khan,Chuanzhu Hu,Tianping Huang,Wenjiang Ding,Jianxin Zou
TMA-TM (TM = Fe, Ni) MOFs were synthesized successfully by a facile method. A MgH2-TM MOF (TM = Fe, Ni) composite was obtained via ball milling and the corresponding hydrogen storage performance was investigated. Particularly, high-resolution transmission electron microscopy was performed to in situ characterize the dehydrogenation behavior of the MgH2-TM MOF composite. The results reveal that nano α-Fe and Mg2NiH4/Mg2Ni derived from the TMA-TM MOFs display a synergetic improving effect on the de/hydrogenation of MgH2. During the hydrogen desorption process, Mg2NiH4/Mg2Ni works as a “hydrogen pump” to quickly deliver hydrogen and facilitates hydrogen diffusion. Meanwhile, α-Fe accelerates the nucleation and growth of Mg by reducing the nucleation energy of Mg from MgH2. The hydriding activation energy of the MgH2-TM MOF declines to 45.3 kJ mol−1 H2. Meanwhile, the peak dehydriding temperature of the MgH2-TM MOF is 530.9 K, which is much lower compared with the MgH2–Fe MOF composite (541.7 K) and as-milled MgH2 (685.2 K). Therefore, nano Mg2Ni and α-Fe derived from the TMA-TM MOFs can remarkably improve the hydrogen storage properties of the MgH2/Mg system due to their synergetic catalytic effects.
研究领域:
材料科学
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能源科学
✓ 已验证
DOI
高影响因子
PROPELLANTS EXPLOSIVES PYROTECHNICS
·
2018
·Vol. 43
·期 7
·637-641
·
IF 1.749
Naimeng Song,Jianchao Liu,Guoying Zhang,Zhenzhan Yan,Hongxu Gao,Li Yang
This paper describes the preparation of two combustion catalysts Tannin-Fe (Ta−Fe) and Phloroglucinol-Fe (Ph−Fe) by spray drying. The particle size and morphology of the particles are observed by scanning electron microscopy (SEM). The results of SEM image show that the particles are regular spherical and very good dispersion. The diameter of most spherical particles is about 1 μm. The effects of Ta−Fe and Ph−Fe on the thermal decomposition of RDX and AP were tested by differential scanning calorimeter (DSC). DSC dates show that Ta−Fe and Ph−Fe can advance the high temperature exothermic peak of AP 18.0 °C and 16.1 °C, respectively. The burning rates illustrates that both Ta−Fe and Ph−Fe can significantly increase the combustion rate of HTPB propellants. The formulation with 2 mass% Ta−Fe shows an average 21.31 % increase in burning rate and has a low value of the exponent n=0.48. The formulation with 2 mass%Ph−Fe has a burning rate 20 to 60 % larger than that of the initial AP/HTPB/Al formulation, and has a lowest exponent n=0.45.
研究领域:
材料科学
·
燃烧与推进
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2021
·
IF 8.128
Chenjie Ding,Shifei Kang,Wenxin Li,Weikang Gao,Zhihao Zhang,Lulu Zheng,Lifeng Cui
Heterogeneous photo-Fenton catalysts prepared by doping metal ions in g-C 3 N 4 are promising alternatives to traditional homogeneous Fenton catalysts, but are restricted by poor mesoporous structure and agglomerate of metal species. Recently, the highly uniformly dispersed metal-N active sites in various photocatalysts have been proved to be the critical reason for their enhanced catalytic activity. In this study based on reasonable control of mesoporous structure and metal-N active sites, mesoporous Fe-g-C 3 N 4 was synthesized using a simple one-step thermal shrinkage polymerization method using ferrous oxalate as iron source and pore-forming agent. The Fe and N elements in the triazine ring skeleton of Fe-g-C 3 N 4 form a σ-π bond, thus the photogenerated electrons can be quickly transferred to Fe 3+ to form Fe 2+ under the interaction of chemical bonds, accelerating the Fenton reaction rate. Density functional theory calculations results demonstrate that the energy band structure and electron cloud density distribution of Fe-Nx active structure are better than that of routine FeOx crystal structure with metal species agglomeration. In addition, the excellent mesoporous structure of Fe-g-C 3 N 4 creates conditions for the high exposure of Fe-Nx active sites in the photo-Fenton reaction under visible light. The as-developed Fe-g-C 3 N 4 system shows high recyclability and excellent photo-Fenton performance for removal of typical intractable pollutants (The degradation rate of dye and tetracycline reaches 98.2% and 98.7% at 60 and 120 min, respectively). This work provides a facile and sustainable route to develop mesoporous highly-active heterogeneous Fenton-like catalysts and even further general the design of general catalyst with ideal metal-N active sites, thereby promoting a feasible and efficient wastewater remediation solution.
研究领域:
环境科学
·
材料科学
·
催化
·
光化学
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2022
·
IF 10.319
Jin-Bo Cheng,Hai-Bo Zhao,Ai-Ning Zhang,Yan-Qin Wang,Yu-Zhong Wang
Nowadays, a large amount of waste fabrics has brought huge environmental and resource problems, while the traditional recycling routes are downcycling with low efficiency and complex separation processes. Herein, we demonstrate a green and facile route to up-recycle waste fabrics (cotton-polyester blending or cotton fabrics) into a high-performance microwave absorber. In this design, an assistant coating was deposited onto the fiber surface of the waste fabric through the assembly of tannic acid-Fe 2+ (TA-Fe 2+ ), which effectively catalyzed the polymer fiber into highly graphitized porous carbon fiber at high temperatures. Meanwhile, the Fe nanoparticles from the reduction of Fe 2+ ions were evenly embedded on the surface of porous carbon fibers. Consequently, the resultant porous carbon/Fe composites with hierarchical microstructures displayed excellent microwave absorption performances. Typically, the microwave absorber from waste polyester-cotton blended fabric could reach a minimum reflection loss ( RL ) of -50.5 dB at a thin coating thickness of 1.7 mm, and the minimum RL from waste cotton fabric absorber reached -47.1 dB at a thickness of 2.5 mm. This work provides a new idea to convert waste fabrics into high value-added microwave absorbing materials in a simple and environmentally friendly way, which will help reuse resources and protect the environment.
研究领域:
环境科学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
ACS Nano
·
2019
·
IF 13.903
Xiang Ao,Wei Zhang,Zhishan Li,Jian-Gang Li,Luke Soule,Xing Huang,Wei-Hung Chiang,Hao Ming Chen,Chundong Wang,Meilin Liu,Xiao Cheng Zeng
Single-atom catalysts (SACs) have emerged as one of the most promising alternatives to noble metal-based catalysts for highly efficient oxygen reduction reaction (ORR). While SACs can offer notable benefits in terms of lowering overall catalyst cost, there is still room for improvement regarding catalyst activity. To this end, we designed and successfully fabricated an ORR electrocatalyst in which atomic clusters are embedded in an atomically dispersed Fe–N–C matrix (FeAC@FeSA–N–C), as shown by comprehensive measurements using aberration-corrected scanning transmission electron microscopy (AC-STEM) and X-ray absorption spectroscopy (XAS). The half-wave potential of FeAC@FeSA–N–C is 0.912 V (versus reversible hydrogen electrode (RHE)), exceeding that of commercial Pt/C (0.897 V), FeSA–N–C (0.844 V), as well as the half-wave potentials of most reported non-platinum-group metal catalysts. The ORR activity of the designed catalyst stems from single-atom active centers but is markedly enhanced by the presence of Fe nanoclusters, as confirmed by both experimental measurements and theoretical calculations.
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED SURFACE SCIENCE
·
2025
·
IF 6.9
Caiyu Ge,Yuefan Wang,Yilin Wang,Zhifang Liu,Chao Chen,Yixi Xie,Pengcheng Zhao,Junjie Fei
As a natural flavonoid compound found in fruits, vegetables and herbs, luteolin (LU) has potent pharmacological activities and beneficial biological properties. Here, a Fe/Zn bimetallic ZIF pyrolysis-derived Fe-Fe 3 O 4 N-doped mesoporous carbon was in-situ grown on carbon nanofibers (Fe-Fe 3 O 4 -NPC@CNFs), and it was used as an ultrasensitive electrochemical sensing platform for the efficient detection of LU in natural samples. Multiple characterization results show that Fe-Fe 3 O 4 -NPC@CNFs is a dodecahedral particle uniformly grown on CNFs with good crystal structure and uniform elemental distribution. Its rough surface with good mesoporous structure and high specific surface area of 823.19 m 2 /g is beneficial for LU adsorption. The density of states (DOS) and adsorption energies of NPC and Fe-Fe 3 O 4 -NPC further demonstrate that Fe-Fe 3 O 4 -NPC has better electrochemical performance and adsorption effect on LU. Under optimized conditions (carbonization: 800℃, pH: 5.0, enrichment: −0.2 V for 400 s), the Fe-Fe 3 O 4 -NPC@CNFs/GCE sensor showed satisfactory detection performance for LU in the range of 0.001–1.5 μM with the limit of detection (LOD) of 0.47 nM. Furthermore, this sensor exhibits excellent anti-interference capability, reproducibility, and stability, and it was also possible to effectively detect LU in food samples. This work provides a new strategy for the quantitative analysis of LU in food.
研究领域:
分析化学
·
材料科学
·
电化学
·
纳米技术
·
食品科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
ENERGY
·
2025
·
IF 9.4
Da Cui,Peng Zhang,Shuang Wu,Hon Man Luk,Yixi Wu,Bin Liu,Shuo Pan,Jingru Bai,Qing Wang,Xuehua Zhang
Oil shale has garnered significant attention as a supplementary energy source to traditional fossil fuels. In this study, we investigated the catalytic hydrothermal liquefaction (HTL) of shale oil sludge using three catalysts (Fe, Na 2 CO 3 , Ni/Al 2 O 3 ) and three combinations in pairs. The hydrothermal oil (HTO) yield, energy recovery (ER), and conversion rate (CR) of organic matters were comprehensively analyzed under six catalyst conditions. Both Fe + Na 2 CO 3 and Fe + Ni/Al 2 O 3 paired catalyst combinations achieved similar HTO yields of 28.43 % and 28.13 % along with ER values of 56.19 % and 57.94 % respectively. Moreover, these two groups achieved remarkably high CR values of 81.88 % and 81.02 %, respectively. The HTO from the Fe + Ni/Al 2 O 3 combination has the highest H/C ratio and the lowest O/C ratio at 1.682 and 0.032, respectively. Elemental composition, Fourier transform infrared spectroscopy (FT-IR), and gas chromatography-mass spectrometry (GC-MS) analyses of HTO were conducted in this study. The HTO produced by using Fe + Ni/Al 2 O 3 exhibited the most ideal distillation distribution, with fractions below diesel accounting for up to 96.94 %. Based on the catalytic functions of Fe, Ni, and Al 2 O 3 , six potential synergistic mechanisms of Fe + Ni/Al 2 O 3 were summarized. These mechanisms highlighted Fe + Ni/Al 2 O 3 's roles in promoting compound conversion pathways in HTO, ultimately revealing the synergistic catalytic mechanism.
研究领域:
能源化学
·
催化科学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）