ANALYTICAL BIOCHEMISTRY
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2019
·
IF 2.507
Ying Jiang,Qi-Meng Yang,Qiu-Ju Xu,Shi-Yu Lu,Lin-Yu Hu,Mao-Wen Xu,Ying-Shuai Liu
Biothiols play critical roles in many biological processes and their aberrant is related to a variety of syndromes. A simple and reliable colorimetric method is developed in this work for biothiols detection based on an oxidase mimic, a metal organic framework (MOF) MIL-53(Fe), and a peroxidase substrate 3,3′,5,5′-tetramethylbenzidine (TMB). In this design, MIL-53(Fe) is utilized to catalyze the conversion of TMB to a blue colored 3,3′,5,5′-tetramethylbenzidine diimine, which can be read on a spectrophotometer at 652 nm. The oxidation-induced blue color generation can be efficiently inhibited by biothiols, thus a colorimetric analytical method is proposed for biothiols detection based on the above system. Under optimal conditions, a linear relationship in a range from 1 to 100 μM and a limit of detection (LOD) at 120 nM are achieved with Cys as a model target. The developed platform is further applied to evaluate cellular biothiols in normal (RWPE-1) and cancer (LNCap) cell lines, revealing that the overall biothiols level in LNCap is much higher than that in RWPE-1. This work renders a powerful tool for identifying cancer cells in a simple manner for biomedical diagnosis associated with biothiols.
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高影响因子
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
·
2019
·Vol. 94
·期 5
·1576-1584
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IF 2.659
Weijie Wen,Zhencheng Lou,Yanjin Chen,Dingsheng Chen,Shuanghong Tian,Ya Xiong
BACKGROUND Iron (Fe) 3+ has much a smaller ion radius than cerium (Ce) 4+ but praseodymium (Pr) ions have a similar radius to Ce ions with the same valence. Hence, it is interesting to tune the structural properties, including lattice deformation, band gap and oxygen vacancy (O v ), of CeO 2 by Pr and Fe codoping for enhanced visible-light catalytic activity. RESULTS A series of Ce 1-x-y Pr x Fe y O 2-σ ( x = 0∼0.012, y = 0.003∼0.031) nanoparticles were prepared by a simple one-step sol-gel method. The structural properties of CeO 2 , including crystal deformation (cell lattice from 5.4069 to 5.4195), band gap (from 2.20 to 2.93), oxygen vacancies (O v from 0.15% to 9.03%), and peroxide species (O 2 2− from 0.37% to 1.09%) can be finely tuned by Pr and Fe codoping. Among ten samples, Ce 0.982 Pr 0.003 Fe 0.015 O 2-σ with proper structural properties showed the highest photocatalytic activity towards the degradation of acid orange 7. The first reaction rate constant reaches 0.0687 min −1 , 9.3 and 7.7 times that of Ce 0.994 Pr 0.006 O 2-σ and Ce 0.985 Fe 0.015 O 2-σ , respectively. The mechanism was found to involve ·OH, ·O 2 − and photogenerated holes. CONCLUSION The structural properties of CeO 2 can be finely and easily tuned by Pr and Fe codoping. Thus, the photocatalytic activity of CeO 2 under visible light irradiation was boosted. © 2019 Society of Chemical Industry
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ADVANCED POWDER TECHNOLOGY
·
2021
·Vol. 32
·期 9
·3364-3371
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IF 4.833
Zigui Luo,Xi'an Fan,Yanglin Zhang,Zhenjia Yang,Jian Wang,Zhaoyang Wu,Xin Liu,Guangqiang Li,Yawei Li
Fe-Si soft magnetic composites (SMCs) coated with MnO-SiO 2 composite coatings were fabricated via sintering the ball milled Fe-Si/MnO 2 composite powders. The transformation mechanism from MnO 2 coating to MnO-SiO 2 composite coatings was studied. The effect of MnO 2 content on the microstructure and magnetic properties of Fe-Si soft magnetic composites has also been investigated systematically. The analysis results indicated that MnO 2 would be reduced to MnO by Si in the Fe-Si particles at 780.1 ℃. When the temperature reached 985.8 ℃, the generated MnO and SiO 2 would further combine to form 2MnO·SiO 2 , finally forming the MnO-SiO 2 composite coatings. With the increase of the MnO 2 content from 0.0 wt% to 10.0 wt%, the MnO-SiO 2 composite coatings became thicker, thus the saturation magnetization and permeability decreased gradually. However, exorbitant MnO 2 content above 5.0 wt% would result in excessive in-situ Fe existed in the composite coatings and obvious reduction of Si content in the Fe-Si particles due to the above solid-state reactions. Therefore, the increasing trend of the resistivity was weakened. And the 5.0 wt% MnO 2 coated Fe-Si SMCs exhibited superior comprehensive performance such as high saturation magnetization (186.5 A·m 2 /kg), good permeability (71), low total core loss (362.6 mW/cm 3 at 50 kHz).
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WATER SCIENCE AND TECHNOLOGY
·
2022
·Vol. 85
·期 7
·2038-2050
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IF 2.43
Zhang Ming,Zhang Kuo,Zhou Runjuan,Wang Jinpeng
In this study, a new type of iron/copper bimetallic combined with hydroxylamine (HA) activated peroxymonosulfate (PMS) was constructed to treat organic pollutants. Selecting the azo dye acid orange 7 (AO7) as the representative of organic pollutants, the new system can achieve nearly 100% degradation of AO7 within 5 min. The Fe(III)/Cu(II)/HA/PMS system mainly generates SO 4 ·− to achieve the degradation of AO7 in acidic environment, while neutral and alkaline environments rely on · OH. The presence of hydroxylamine accelerates the cycle of Fe(III)/Fe(II) and Cu(II)/Cu(I) in the system, and enhances the degradation ability of the system for organic pollutants. The addition of trace Cu(II) (1 μM) enhances the ability of a single Fe(III)/HA/PMS system to degrade AO7 in neutral and alkaline environments without causing secondary copper pollution. The common inorganic anions Cl − and NO 3 − in water have almost no effect on the degradation of AO7 in the system. The constructed Fe(III)/Cu(II)/HA/PMS system is an efficient and clean organic pollutant wastewater treatment process, which has very promising application prospects. The effect of hydroxylamine on the activation of peroxymonosulfate in Fe(III)-Cu(II) bimetallic is reported for the first time. The Fe(III)/Cu(II)/hydroxylamine/peroxymonosulfate system can remove 100% of AO7 within 5 min. Hydroxylamine enables Fe(III), which cannot activate peroxymonosulfate, to activate peroxymonosulfate efficiently. A trace amount of Cu(II) can reduce Fe(III) to Fe(II).
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ChemistrySelect
·
2026
·Vol. 11
·期 37
·e74658
·
IF 2.3
Feifei Xing,Yuheng Jing,Fei Wang,Junfeng Feng,Yuwei Chen,Baining Lin,Rukuan Liu,Jianchun Jiang
Developing low-cost and sulfur-free catalysts is essential for converting waste lipids into green diesel. Herein, hydroxyapatite-supported Ni–Fe catalysts were prepared via a one-step co-precipitation strategy and evaluated for lipid hydrotreatment. The optimized 20Ni–Fe/HAP catalyst delivered 97.1% conversion and 89.1% alkane yield in fatty acid hydrotreatment at 240°C, far outperforming the impregnation-derived counterpart, which gave only 13.1% alkane yield under identical conditions. Characterization results revealed that the superior performance originated from the formation of highly dispersed Ni 3 Fe species, abundant accessible Ni active sites, enlarged surface area, and suitable acidity distribution. Increasing the Ni loading beyond 20 wt.% failed to further improve the activity because of reduced active-site accessibility and pore diffusion efficiency. The catalyst also showed excellent adaptability toward practical feedstocks, affording over 98% alkane yields from used cooking oil and acidified vegetable oil at 260°C. Moreover, 20Ni–Fe/HAP maintained stable performance during five consecutive runs, with negligible changes in conversion and C15–C18 alkane yield. This work provides an efficient Ni–Fe/HAP catalytic system for sustainable production of diesel-range alkanes from waste lipids. Graphical One-step coprecipitation creates a Ni 3 Fe catalyst supported on hydroxyapatite with abundant accessible Ni sites and suitable acidity for efficient lipid hydrotreatment. The optimized 20Ni–Fe/HAP catalyst affords high yields of diesel range alkanes under mild conditions, converts used cooking oil and acidified vegetable oil, and remains stable over five consecutive cycles without noble metals or sulfur.
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2026
·
IF 9.1
Lingzhen Miao,Siqi Luo,Ziru Liang,Ming Lu,Pengcheng Wang
The treatment of wastewater laden with energetic compounds, particularly 2,2′,4,4′,6,6′-hexanitrostilbene (HNS), remains highly challenging owing to the environmental persistence and inherent toxicity of nitroaromatic derivatives. Herein, we reported a CoFe 2 O 4 /PMS system for the first-time efficient degradation of HNS. The CoFe 2 O 4 /PMS process afforded 96.3% removal of HNS within 150 min, together with 89.3% chemical oxygen demand (COD) removal and 49.5% total organic carbon (TOC) removal, indicating substantial deep oxidation and partial mineralization. Mechanistic studies combining quenching experiments, EPR spectroscopy, electrochemical analysis, and DFT calculations disclosed a synergistic radical/non-radical pathway dominated by 1 O 2 , with Fe incorporation enhancing PMS adsorption, charge transfer, and catalytic activation. HPLC-MS revealed degradation intermediates and supported three plausible degradation pathways, whereas QSAR analysis indicated progressive detoxification during oxidation. The catalyst further exhibited excellent stability, negligible metal leaching, and broad applicability toward actual HNS production wastewater and other energetic organic pollutants. These findings identify CoFe 2 O 4 /PMS as a promising platform for the efficient remediation of hazardous energetic compound wastewater.
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高影响因子
JOURNAL OF FLUORESCENCE
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2026
·
IF 3.4
Hou Huijing,Luo Mingming,Li Fang,Tan Yijun,Liu Ruowei,Xu Longping,Feng Yanwen,Guo Xiangli,Wu Zijian
Kanamycin (KANA) is a veterinary drug residue that is highly scrutinized in food safety testing. In this study, a metal-organic framework-based aptamer-nanoenzyme (NH 2 -MIL-88B(Fe)/CDs-Apt) was introduced for the dual-mode detection of KANA. NH 2 -MIL-88B(Fe) catalyzes the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) by H₂O₂ to form blue ox-TMB, thereby enabling colorimetric detection. As a fluorescence quencher, NH 2 -MIL-88B(Fe) quenches the fluorescence of CDs via photogenerated electron transfer (PET) or fluorescence resonance energy transfer (FRET) mechanisms. The detection limits were 0.716 fM (fluorescent) and 0.709 fM (colorimetric), respectively. The proposed aptasensor was successfully applied to the detection of KANA in eggs, honey, and lake water. This aptasensor demonstrates high sensitivity and accuracy, as well as broad application potential.
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DOI
PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2026
·
IF 19.7
Yifei Liu,Defa Liu,Ying Yu,Zumin Wang,Ruziev Umidjon Abdimajitovich,Donaev Sardor Burkhanovich,Semencha Alexander Vyacheslavovich,Lei Wang,Lingbo Zong,Bin Li,Xufang Qian
Fe-Cu dual-atom sites were prepared through pre-coordination and ultrafast Joule heating. • FeCu-N-MCS displays a large E 1/2 , low H 2 O 2 yield and excellent stability. • FeCu-N-MCS suppresses H 2 O 2 accumulation through hydrogen peroxide reduction reaction (HPRR). • Cooperative interaction of dual-atom sites reduces the energy barrier of OH* desorption for 4e⁻ ORR. • Zn-air batteries achieve ultrahigh power density and remarkable charge/discharge stability. The oxygen reduction reaction (ORR) governs the power output and cycling lifetime of metal-air batteries. Fe-N-C single-atom catalysts are among the most promising precious-metal-free ORR electrocatalysts, but their durability is often compromised by H 2 O 2 generated through the competing two-electron ORR pathway, which can trigger Fenton reactions and radical-induced catalyst degradation. Herein, Fe-Cu dual-atom sites anchored on microporous carbon spheres (FeCu-N-MCS) are constructed through a pre-coordination strategy followed by rapid Joule heating. Combined experimental results and density functional theory (DFT) calculations reveal that the electronic coupling between Fe and Cu sites lowers the energy barrier of the rate-determining step for the four-electron ORR pathway. More importantly, the Fe-Cu dual-site configuration enables spontaneous hydrogen peroxide reduction reaction (HPRR) at Fe sites and significantly facilitates OH* desorption during HPRR, thereby suppressing H 2 O 2 accumulation and alleviating Fenton-type oxidative degradation. Consequently, FeCu-N-MCS delivers outstanding ORR performance with a half-wave potential of 0.91 V, a low H 2 O 2 yield below 2.91%, and 91.05% current retention after 100 h. Aqueous Zn-air batteries (A-ZABs) assembled with FeCu-N-MCS achieve a peak power density of 223.73 mW cm −2 and stable cycling for over 1200 h. FeCu-N-MCS-based Quasi-solid-state ZABs (QSS-ZABs) further exhibit an open-circuit voltage (OCV) of 1.52 V and a power density of 246.85 mW cm −2 . This work establishes a dual-atom-site strategy for coupling high ORR activity with H 2 O 2 -resistant durability, offering mechanistic insight into the design of robust precious-metal-free electrocatalysts for advanced metal-air batteries. Download: Download high-res image (220KB) Download: Download full-size image Fe-Cu dual-atom sites were prepared through pre-coordination and Joule heating. The incorporation of Cu sites into Fe-N-MCS not only reduces the energy barrier of the rate-determining step (RDS) to accelerate the 4e⁻ ORR pathway, but also enables spontaneous hydrogen peroxide reduction reaction (HPRR) to suppress H 2 O 2 accumulation and Fenton corrosion. Consequently, the assembled Zn-air batteries achieve remarkable power density and ultra-long cycling stability.
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高影响因子
Foods
·
2026
·Vol. 15
·期 16
·2886
·
IF 6
Luyao Wang,Xuelian Wu,Yizi Mahai,Wenjing Ma,Lin Zhou,Jing Zhang,Xinhui Wang,Jing Li
Monitoring dopamine (DA) in pork can provide useful information for assessing meat freshness and quality deterioration. In this work, an Fe@N-S-O-C nanocomposite was fabricated as an electrode modifier for DA determination. The Fe@N-S-O-C nanocomposite was synthesized via precipitation followed by calcination using melamine and ferrous sulfate as precursors. The crystal structure, surface chemical composition, and morphology were characterized by XRD, XPS, SEM, and TEM. The Fe@N-S-O-C-modified glassy carbon electrode (Fe@N-S-O-C/GCE) was then evaluated for its electrocatalytic performance toward DA. Under the optimized conditions (pH 6.0), the sensor showed linear responses to DA over 1–65 and 65–220 μM. The sensitivities for these two ranges were 4.357 and 1.685 μA μM−1cm−2, respectively, with an LOD of 40 nM. In addition, the Fe@N-S-O-C/GCE showed excellent reproducibility, good repeatability, and strong anti-interference capability against common coexisting substances. After 30 days of storage, 82.74% of the initial current response was retained by the same electrode. Practical applicability of the sensor was verified in pork samples, with recoveries of 95.97–106.73%. These results demonstrate that the Fe@N-S-O-C/GCE sensor offers a reliable and effective platform for DA detection in complex food matrices.
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高影响因子
JOURNAL OF POWER SOURCES
·
2026
·
IF 8.4
Ruite Gu,Tingyu Yan,Zeyu Hao,Huanlu Tu,Shansheng Yu,Xiaoying Hu,Hongwei Tian
The preparation of highly efficient, stable, and cost-effective catalysts to address the complex oxygen reduction reaction (ORR) in zinc-air batteries remains a significant challenge. Herein, a surface modification strategy is employed to uniformly encapsulate an Fe-N-C matrix with cobalt-coordinated conjugated organic polymers containing Schiff base structures, successfully yielding a highly active CB(cobalt-coordinated Schiff-base polymer)@Fe-N-C composite catalyst with coexisting cobalt coordination polymers and iron-nitrogen-carbon structures. In alkaline electrolytes, the CB@Fe-N-C catalyst exhibits outstanding catalytic activity (E 1/2 = 0.93 V) and stability, which are attributed to its highly conductive, structurally stable composite architecture with abundant active sites. In a zinc-air battery (ZAB), CB@Fe-N-C exhibits remarkable power density, surpassing the Pt/C benchmark. This work offers an effective synthetic strategy for preparing electrocatalysts with excellent ORR performance in zinc-air batteries.
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高影响因子
APPLIED SURFACE SCIENCE
·
2026
·
IF 6.6
Yunxu Yang,Xiaoxi Huang,Yong Shen Chua,Hooi Ling Lee
Fe–SnO 2 @NiO–NF removed 96.85% CIP within 150 min under solar light. • S-scheme heterojunction promotes charge separation and photocatalytic activity. • 3D NiO–NF support enables easy recovery and abundant active sites. • Over 94% degradation activity was retained after four cycles. • DFT and HPLC–MS reveal charge transfer and CIP degradation pathways. Photocatalysis is effective for antibiotic degradation but limited by poor charge separation and difficult recovery of powder catalysts. In this work, a macroscopic p–n heterojunction photocatalyst (Fe–SnO 2 @NiO–NF) was prepared on pre-oxidized nickel foam through in situ growth and microwave-assisted synthesis. XRD confirmed the coexistence of SnO 2 and NiO phases, while HRTEM and XPS analyses verified the successful construction of the Fe–SnO 2 /NiO heterojunction with intimate interfacial contact and interfacial electronic interaction. UV–vis DRS, PL, TRPL, EIS, and photoelectrochemical measurements demonstrated markedly improved light absorption, charge separation and transfer behavior, with a narrowed band gap of 2.92 eV and a prolonged average carrier lifetime of 1.2226 ns. Owing to the enhanced charge separation and the conductive 3D NiO–NF framework, Fe–SnO 2 @NiO–NF exhibited significantly improved photocatalytic activity for ciprofloxacin degradation under solar irradiation, reaching 96.85% removal within 150 min, while the immobilized catalyst could be readily separated from the aqueous solution. ESR and scavenging test identified •O 2 – and h + as the main reactive species, with •O 2 – playing the dominant role, while HPLC–MS revealed the degradation intermediates and pathways. Band structure analysis and DFT calculations demonstrated that the p–n heterojunction follows an S-scheme charge transfer mechanism, promoting efficient charge separation while preserving strong redox capability. The composite retained over 94% of its initial activity after four cycles, showing excellent stability and recyclability. This study provides a practical way to develop efficient and reusable photocatalysts for antibiotic wastewater treatment. Download: Download high-res image (182KB) Download: Download full-size image
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2026
·
IF 6.7
Jian Wang,Chengliang Zhao,Fang Wang,Lei Xie,Chong Tan,Zigui Luo,Haibo Sun,Chuntao Chang
This work presents the fabrication of low-loss, high-permeability Fe-Si soft magnetic composites (SMCs) utilizing alumina-coated and subsequently annealed Fe-Si powder. Appropriate annealing preserves a uniform, dense, and continuous alumina insulating layer, enabling optimization of the magnetic properties through powder annealing. The optimal annealing duration for Fe-Si SMCs was identified as 180 min, yielding a minimum core loss of 259.1 mW/cm 3 and a peak permeability of 94.85 (measured at 50 mT/100 kHz). The observed reduction in hysteresis loss arises from the combined influence of grain growth and stress relaxation during the annealing process. A uniform insulating layer effectively restricts induced eddy currents to individual powder particles, thereby minimizing eddy current losses. However, prolonged annealing compromises the coating’s structural integrity, resulting in a decline in magnetic performance. This work introduces a systematic strategy for enhancing the overall magnetic properties of SMCs by precisely controlling the annealing time of the powders, establishing a distinct correlation between coating evolution and composite performance. These insights provide practical direction for the high-efficiency deployment of soft magnetic composites in high-frequency magnetic applications.
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高影响因子
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