BIORESOURCE TECHNOLOGY
·
2024
·
IF 9.7
Qiushi Jiang,Yanjing Li,Minmin Wang,Wen Cao,Xueying Yang,Sihu Zhang,Liejin Guo
This study investigated the mediating effect of Triethanolamine on Fe@C- Rhodobacter sphaeroides hybrid photosynthetic system to achieve efficient biohydrogen production. The biocompatible Fe@C generates excited electrons upon exposure to light, releasing ferrum for nitrogenase synthesis, and regulating the pH of the fermentation environment. Triethanolamine was introduced to optimize the electron transfer chain, thereby improving system stability, prolonging electron lifespan, and facilitating ferrum corrosion. This, in turn, stimulated the lactic acid synthetic metabolic pathway of Rhodobacter sphaeroides , resulting in increased reducing power in the biohybrid system. The ternary coupling system was analyzed through the regulation of concentration, initial pH, and light intensity. The system achieved the highest total H 2 production of 5410.9 mL/L, 1.29 times higher than the control (2360.5 mL/L). This research provides a valuable strategy for constructing ferrum-carbon-based composite-cellular biohybrid systems for photo-fermentation H 2 production.
研究领域:
微生物学
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可再生能源
·
光合作用
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产品关联
DOI
PubMed
高影响因子
ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2018
·
IF 6.653
Jing Chen,Nannan Wu,Xinxin Xu,Ruijuan Qu,Chenguang Li,Xiaoxue Pan,Zhongbo Wei,Zunyao Wang
Potassium ferrate [Fe(VI)] is a promising oxidant widely used in water treatment for the elimination of organic pollutants. In this work, the reaction kinetics, products, and mechanisms of the antimicrobial agent chlorophene (CP) undergoing Fe(VI) oxidation in aqueous solutions were investigated. CP is very readily degraded by Fe(VI), with the apparent second-order rate constant, k, being 423.2 M–1 s–1 at pH 8.0. A total of 22 oxidation products were identified using liquid chromatography–quadrupole time-of-flight–mass spectrometry , and their structures were further elucidated using tandem mass spectrometry. According to the extracted peak areas in mass spectra, the main reaction products were the coupling products (dimers, trimers, and tetramers) that formed via single-electron coupling. Theoretical calculations demonstrated that hydrogen abstraction should easily occur at the hydroxyl group to produce reactive CP· radicals for subsequent polymerization. Cleavage of the C–C bridge bond, electrophilic substitution, hydroxylation, ring opening, and decarboxylation were also observed during the Fe(VI) oxidation process. In addition, the degradation of CP by Fe(VI) was also effective in real waters, which provides a basis for potential applications.
研究领域:
环境科学
·
化学
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产品关联
DOI
PubMed
高影响因子
ENVIRONMENTAL POLLUTION
·
2019
·
IF 5.714
Zhao Yang,Xu Zhang,Siji Pu,Renxiang Ni,Ying Lin,Yong Liu
A novel heterogeneous Fenton-like system (Mg/Fe-O 2 ) which could directly convert oxygen (O 2 ) to hydrogen peroxide/hydroxyl radicals (H 2 O 2 / • OH) was developed and used to degrade 4-chlorophenol. The Mg/Fe bimetallic particles were prepared by chemical displacement process and characterized by XRD, SEM and TEM. The in situ continuous production of H 2 O 2 / • OH and the effect of the mole ratio of Mg to Fe in the Mg/Fe bimetallic particles and the operating parameters on the degradation 4-chlorophenol in Mg/Fe-O 2 system were investigated in detail. It was found that the Mg/Fe bimetallic particles with the mole ratio of Mg to Fe of 32:1 had the best performance for the 4-chlorophenol degradation and the maximum cumulative concentration of H 2 O 2 , the degradation efficiency of 4-chlorophenol and the removal efficiency of TOC in Mg/Fe-O 2 system were 34.5 mg/L, 100% and 91.8%, respectively, at pH 3, O 2 flow rate 400 mL/min, dosage of Mg/Fe bimetallic particles 2 g/L, 4-chlorophenol initial concentration 50 mg/L and reaction time 60 min. It was revealed by radical scavenging experiments that • OH, particularly the surface-bound • OH, were the predominant reactive oxygen species in Mg/Fe-O 2 system for the degradation of 4-chlorophenol. The main intermediates of 4-chlorophenol degradation were detected by high-resolution liquid chromatography equipped with time-of-flight mass spectrometry (HRLC–ToF-MS) and ion chromatography (IC). Based the results of control experiments and the electrochemical tests, the possible pathway and mechanism of 4-chlorophenol degradation in Mg/Fe-O 2 system were tentatively proposed.
研究领域:
环境科学
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化学工程
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DOI
PubMed
高影响因子
Journal of Materials Chemistry A
·
2021
·Vol. 9
·期 42
·23817-23827
·
IF 12.732
Manman Feng,Xuemei Wu,Huiyuan Cheng,Zihao Fan,Xiangcun Li,Fujun Cui,Shuai Fan,Yan Dai,Guangping Lei,Gaohong He
The diatomic catalysts (DACs) provide a new strategy for efficient catalysis of CO2 reduction reaction (CO2RR) owing to their maximum atomic utility and more flexible active sites. However, it is still challenging to precisely design heteronuclear diatomic active centers and understand the coordination mechanism of binary sites at the atomic level. Herein, a nitrogen-doped carbon matrix with precisely controlled Fe–Cu diatom sites is synthesized through a metal–organic framework. The as-obtained Fe/Cu–N–C catalyst exhibits an excellent CO faradaic efficiency (>95% over a wide potential range of −0.4 to −1.1 V vs. RHE, 99.2% at −0.8 V vs. RHE), a high turnover frequency (5047 h−1 at −1.1 V vs. RHE), and a low overpotential (50 mV), thus outperforming most reported atomically dispersed catalysts. Further density functional theory calculations indicate that the synergy between Fe–Cu diatoms causes rapid charge transfer and effectively adjusts the position of the d-band center, which reduces the energy barriers for *COOH formation and *CO desorption. This work provides a new approach for advancing universal synthesis strategies to construct heteronuclear diatomic catalysts and explore synergistic effects.
研究领域:
材料科学
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催化化学
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能源转换
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DOI
高影响因子
Acta Biomaterialia
·
2022
·
IF 10.633
Xian Tong,Li Zhu,Yihao Wu,Yiting Song,Kun Wang,Shengbin Huang,Yuncang Li,Jianfeng Ma,Cuie Wen,Jixing Lin
Zinc (Zn)-based metals and alloys are emerging as promising biodegradable implant materials due to their inherent biodegradability and good biocompatibility. However, this class of materials exhibits low mechanical strength and a slow degradation rate, which hinders their clinical application. Here we report the development of a new biodegradable Fe/Zn–3Cu composite fabricated by infiltration casting of a Zn–3Cu alloy into an Fe foam followed by hot-rolling. Our results indicate that the hot-rolled (HR) Fe/Zn–3Cu composite exhibited an α-Zn matrix phase, a secondary CuZn 5 phase, and an α-Fe phase. The HR Fe/Zn–3Cu composite exhibited an ultimate tensile strength of 269 MPa, a tensile yield strength of 210 MPa, and an elongation of 27%. The HR Fe/Zn–3Cu composite showed a degradation rate of 228 µm/year after immersion in Hanks’ solution for 30 d The diluted extract of the HR Fe/Zn–3Cu composite exhibited a higher cell viability than that of the HR Zn–3Cu alloy in relation to MC3T3-E1 and MG-63 cells. Furthermore, the HR Fe/Zn–3Cu composite showed significantly better antibacterial ability than that of the HR Zn–3Cu alloy in relation to S. aureus . Overall, the HR Fe/Zn–3Cu composite can be anticipated to be a promising biodegradable implant material for bone-fixation applications. Statement of significance This work reports a new biodegradable Fe/Zn–3Cu composite fabricated by infiltration casting and followed by hot-rolling for biodegradable bone-fixation application. Our findings demonstrated that the hot-rolled (HR) Fe/Zn–3Cu composite exhibited an ultimate tensile strength of 269.1 MPa, a tensile yield strength of 210.3 MPa, and an elongation of 26.7%. HR Fe/Zn–3Cu composite showed a degradation rate of 227.6 µm/a, higher than HR Zn–3Cu alloy after immersion in Hanks’ solution for 30 d The diluted extracts of the HR Fe/Zn–3Cu composite exhibited a higher cell viability than HR Zn–3Cu alloy toward MC3T3-E1 cells. Furthermore, the HR Fe/Zn–3Cu composite showed significantly better antibacterial ability than the HR Zn–3Cu alloy toward S. aureus .
研究领域:
生物医学工程
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材料科学
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骨科应用
✓ 已验证
DOI
高影响因子
CARBON
·
2021
·
IF 9.594
Zhouyu Tong,Zijian Liao,Yanyan Liu,Mingliang Ma,Yuxin Bi,Weibo Huang,Yong Ma,Mingtao Qiao,Guanglei Wu
Designing one-dimensional (1D) magnetic-carbon composites microwave absorbers is a promising strategy that can meet the current demand for high-performance microwave absorption (MA) materials. In this work, hierarchical structured Fe 3 O 4 /Fe@C@MoS 2 nanofibers were successfully obtained via a simple three-step method. 1D Fe 3 O 4 /Fe@C nanofibers were fabricated through electrospinning technology and in-situ polymerization followed by carbonization and reduction in H 2 /N 2 atmosphere. MoS 2 nanosheets grew irregularly on the surface of 1D Fe 3 O 4 /Fe@C nanofibers to form the flower-like structure. The morphology, composition and magnetism of samples were systematically investigated. Furthermore, electromagnetic characteristics and MA properties of Fe 3 O 4 /Fe@C nanofibers and Fe 3 O 4 /Fe@C@MoS 2 nanofibers were compared. The minimum reflection loss (RL min ) of Fe 3 O 4 /Fe@C@MoS 2 nanofibers could reach −53.79 dB at 11.12 GHz and the corresponding absorption bandwidth (RL < -10 dB) of 4.4 GHz was achieved at the absorber thickness of 2.24 mm. This work combines electrospinning technology with traditional chemical synthesis to prepare a novel 1D core-shell microwave absorber, which provides some inspiration for preparing MA material in the future.
研究领域:
材料科学
·
电磁学
·
化学合成
✓ 已验证
DOI
高影响因子
CATALYSIS LETTERS
·
2024
·Vol. 154
·期 8
·4088-4095
·
IF 2.3
Li Ling,Yan Shasha,Wang Hui,Ge Xingbo
The oxygen evolution reaction (OER) plays a vital role in electrolytic water splitting. It is urgent to explore highly active non-precious metal OER catalysts. Herein, the etching combined with the electrodeposition was used to synthesize the efficient Ni–Fe/p-CoAl catalyst, which exhibits ideal OER performance. A low overpotential of 282 mV and 296 mV are needed to achieve the current density of 50 mA/cm 2 and 100 mA/cm 2 in 1 M KOH, respectively. Moreover, the as-prepared catalyst shows good durability with no detectable degradation during long-term operation. The enhanced OER performance can be attributed to the large electrochemical surface area and the strong interaction between Ni–Fe nanosheets and active substrate. Graphical Abstract Etching combined with the electrodeposition method was used to synthesize an efficient Ni–Fe/p-CoAl catalyst for OER.
研究领域:
材料科学
·
电化学
✓ 已验证
DOI
高影响因子
COMPOSITES PART B-ENGINEERING
·
2019
·
IF 6.864
Zhiming Deng,Yue Li,Hao-Bin Zhang,Yu Zhang,Jia-Qi Luo,Liu-Xin Liu,Zhong-Zhen Yu
Lightweight and high-performance microwave absorption materials with wide effective bandwidth are highly required due to the increasingly severe electromagnetic radiation. It is now still imperative to elaborately tune the constituents and microstructures of absorbers for improving microwave absorption capability over wide frequency ranges. Herein, sulfonated polystyrene@Fe(OH) 3 @polydopamine (SPS@Fe(OH) 3 @PDA) microspheres are firstly synthesized with ferric sulphate and dopamine as precursors of Fe(OH) 3 and amorphous carbon , and then thermally annealed at 600 °C to generate lightweight Fe@C hollow microspheres. The thermal annealing effectively decomposes SPS templates to gases, and carbonizes the PDA shell to amorphous carbon, which also reduces the ferric irons to magnetic Fe nanoparticles via the carbothermal reduction reaction. Interestingly, the microwave absorption performances of the Fe@C hollow microspheres are obviously improved by increasing the cavity sizes. The Fe@C hollow microspheres with the largest cavity of 780 nm exhibit the broadest effective absorption bandwidth of 7.5 GHz and the superior maximum reflection loss of −37.7 dB. These outstanding performances are attributed not only to the favourable synergistic effect of dielectric and magnetic losses, but also to the optimized hollow structure enhancing the attenuation capability and improving impedance matching. This work provides an efficient approach for designing and fabricating high-performance and broad-band microwave absorbers with tunable peak frequency.
研究领域:
材料科学
·
电磁学
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF REFRACTORY METALS & HARD MATERIALS
·
2020
·
IF 3.407
Youhong Sun,Jinhao Wu,Linkai He,Baochang Liu,Chi Zhang,Qingnan Meng,Xuliang Zhang
Diamond/WC-Fe-Ni composite is a potential composition for impregnated diamond drill bits. It is necessary to avoid the graphitization of the diamond from Fe and Ni under the powder metallurgy process. Boron carbide (B 4 C) was coated on diamond, and diamond/WC-Fe-Ni composites were consolidated by hot pressing at different temperatures. The influences of sintering temperature and interfacial structure on bending strength and wear behavior were investigated. The bending strength for diamond/WC-Fe-Ni composite was dependent on matrix densification and interfacial graphitization. Un-coated diamond was eroded by Fe-Ni matrix and partially converted to graphite during the sintering process at all sintering temperatures. In opposite, B 4 C coating was beneficial to matrix densification at a lower sintering temperature, and delayed the appearance of graphitization to around 1300 °C. Therefore, the diamond/WC-Fe-Ni composites with B 4 C coating exhibited larger bending strength and better wear behavior at a relative low sintering temperature.
研究领域:
材料科学
·
矿物工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ENVIRONMENTAL MANAGEMENT
·
2018
·
IF 4.005
Yi Hu,Yulian Li,Junyong He,Tao Liu,Kaisheng Zhang,Xingjiu Huang,Lingtao Kong,Jinhuai Liu
Industrial waste, urban sewage and aquaculture have led to severely increased grades of environment pollutants such as dyes, pesticides and fertilizer. The use of technologies for purifying contaminated waters can be difficult and toxic due to the anti-photolysis, anti-oxidation and anti-bio-oxidation characteristics of organic pollutants, and there is therefore a significant need for new approaches. Here, we report methods of Fenton oxidation and EDTA-Fe(III) Fenton-like oxidation which can be used to degrade malachite green (MG: a dye and antibiotic-like substance) from contaminated water. Compared with the degradation rate (59.34%) of the Fe(III)/H 2 O 2 Fenton process, the EDTA-Fe(III) Fenton-like oxidation got a better degradation rate (92.7%) at neutral pH conditions . By conducting a series of parallel controlled experiments (changing parameters such as the reactant concentration , temperature, and pH), we report the relationships between the degradation effect and different parameters, and we fitted their pseudo first order kinetic curves. Furthermore, we repeated to adjustment of the concentrations of MG in solutions to test the cycle performance and catalytic activities of EDTA-Fe(III)/H 2 O 2 system and it showed good repeatability in the first five rounds and all of them keep the degradation efficiencies greater than 80%. By conducting comparative spin-trapping electron paramagnetic resonance (EPR) experiments, we showed indirectly that the OH contributes to the degradation of MG. Additionally, the results of the EPR experiments showed that EDTA contributes to the generation of OH in the EDTA-Fe(III)/H 2 O 2 Fenton-like system. By conducting total organic carbon (TOC) analysis experiments, we found that EDTA was also oxidized to some extent during the degradation of MG. In all, the findings of this work widen the range of the optimal pH values up to neutral condition for degradation of MG by use of EDTA-Fe(III) Fenton-like system. And this system could be used as one approach for the degradation of organic pollutants at neutral conditions and provide some initial information regarding EDTA-Fe(III) Fenton-like oxidations. It's significant for the expansion of the homogenous Fenton-like family and its application in the field of water treatment .
研究领域:
环境科学
·
化学工程
·
水处理技术
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF FOOD COMPOSITION AND ANALYSIS
·
2025
·
IF 4.6
Xueyi Ren,Honglei Tian,Jianke Li,Yuhuan Zhang
Colorimetric detection methods are prosperous in the monitoring of contaminants in food and environmental matrices. However, the traditional single-channel color changes seriously restrict the enhancement of their sensitivity and facile applications. Herein, a Fe 3+ concentration-controlled dual-channel ratiometric colorimetric sensing platform for the sensitive detection of Pb 2+ was established. Generally, the low concentrations of Fe 3+ can trigger a typical absorption peak at 652 nm of the oxidized TMB (oxTMB). While high concentrations of Fe 3+ induce colorless-to-orange change due to the generation of biphenyl quinone with strong absorption peaks at 450 nm. Interestingly, the presence of Pb 2+ could convert Fe 3+ to Fe (3+x)+ by a displacement reaction, causing a blue-to-colorless change at low Fe 3+ concentrations or an orange-to-blue color change at high Fe 3+ concentrations. The latter dual-channel color variances corresponded to a more distinguished visual quantification of Pb 2+ compared to the former one-channel changes. As such, the Pb 2+ was detected over a range of 0.625-25 µM, with a low detection limit (LOD) of 70 nM. Additionally, by integrating smartphone optical equipment and color recognition software, an intelligent platform for the instant detection of Pb 2+ was established, with a LOD of 0.30 µM. In real samples detection, the developed smartphone sensing platform demonstrated excellent recovery rates (89.0±4.6% to 111.1±7.4%), comparable to the conventional UV-Vis spectroscopy. This work sheds light on fabrication dual-channel colorimetric detection methods for enhanced sensing performance and provides a rapid, sensitive, and intelligent platform for detecting small molecular hazards in the environment.
研究领域:
分析化学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
SCIENCE OF THE TOTAL ENVIRONMENT
·
2021
·
IF 7.963
Xiaoling Ma,Wenlong Wang,Chenggong Sun,Hui Li,Jing Sun,Xin Liu
In light of the promising merits of large surface area, uniform pore size, and tunable functional groups, metal-organic frameworks (MOFs) have great potential to be utilized for adsorbing volatile organic compounds (VOCs). In this study, three Fe-based MOFs, MIL-100(Fe), MIL-101(Fe), and MIL-53(Fe), were synthesized systematically and used to adsorb a typical VOC, toluene. Static adsorption, dynamic breakthrough curves , and adsorption kinetics were conducted to assess the adsorption performance. Additionally, the surface functional groups, pore structure, and morphology were systematically characterized by means of XRD , SEM, XPS, FTIR and N 2 adsorption-desorption analyses to reveal the cause of the difference in adsorption of these Fe-based MOFs. The results revealed that the maximum equilibrium adsorption capacity of 663 mg/g was achieved by MIL-100(Fe) with the highest specific surface area and pore volume. The dynamic adsorption of toluene on MIL-100(Fe) was in accordance with the pseudo-first order kinetic model and the Langmuir isothermal model. The formed π-π stacking interaction between organic ligands and the benzene ring in the MIL-100(Fe) cluster is the primary adsorption mechanism based on XPS analysis. Moreover, MIL-100(Fe) was easily regenerated via microwave irradiation with a negligible adsorption capacity decrease after three cycles. This work highlights the feasibility of hierarchical porous Fe-based MOFs as toluene adsorbents and promotes the application of MOFs in the field of pollution control .
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）