CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Shiyong Wei,Aijia Cao,Siyuan Huang,Yao Shen,Ting Lei,Songmei Luo,Mingjun Cai,Wenjun Xiang,Anying Chen,Rui Wang
Although MIL-100(Fe) was regarded as an ideal material for the environmental remediation, it could not be applied in practical because of the potential eco-environmental risk and cost. In this work, a novelty strategy of liquidizing crystal MIL-100(Fe) was posted for the first time through inhibiting the crystallization process and forming physical MIL-100(Fe) gel. Due to this MIL-100(Fe) sol–gel, MIL-100(Fe) could easy cover on the surface of silica powder (SiO 2 ) through simple soaking operation. MIL-100(Fe) covering on SiO 2 (MIL-100(Fe)@SiO 2 ) could be quickly separated from wastewater spontaneously owing to the carrier of SiO 2 , even in a tank of 2.0 m, which made it possible for purifying wastewater in practical. MIL-100(Fe)@SiO 2 could remove phosphate with a removing ratio of closing 100 % at an initial concentration of 10 mg/L, while more than 95 % towards methyl orange (MO). The removing ratio of MO by MIL-100(Fe)@SiO 2 did not obviously decrease when the concentration of MO increased to 100 mg/L. And the adsorption performance of phosphate did not affect by pH among 3.0–9.0. The adsorption amount exceeded 50 % of maximum adsorption capacity for phosphate within 30 min, while 90 % for MO. Monodentate mononuclear coordination could explain the adsorption of phosphate by MIL-100(Fe)@SiO 2 . The N atom in MO might be acted as Lewis acid to coordinate with MIL-100(Fe)@SiO 2 . After adsorption, the P-saturated and MO-saturated MIL-100(Fe)@SiO 2 could be effectively regenerated by the dilute HCl and NaOH solution, respectively. The recovery ratio of adsorption capacity for phosphate and MO were up to 97.7 % and 71.6 %.
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MICROPOROUS AND MESOPOROUS MATERIALS
·
2022
·
IF 5.876
Xiuying Zhu,Mengjie Li,Xiong-Fei Zhang,Jianfeng Yao
Iron-based metal-organic framework (MIL-100) with intrinsic high surface area and low cost is extremely attractive in the field of organic pollutant remediation. Herein, delignified balsa wood is utilized as substrate/support for the in situ growth and dispersion of MIL-100 particles. Results demonstrate that the MIL-100 particles adhere tightly to the support and a hierarchal architecture is constructed. The MIL-100@Wood composite can be used as adsorbent and filter for the alleviation of organic contamination. With 25.4 wt% of MIL-100 loading, the MIL-100 decorated delignified wood (MD-Wood) exhibits a tetracycline (TC) adsorption capacity of 109.9 mg/g. The composite MD-Wood can be easily fabricated into an all-in-one filter and this filter presents an effective treatable volume of 1100 mL of TC solution (20 mg/L). The MD-Wood is further deposited with Ag particles and the Ag@MD-Wood can be directly applied for the flow catalytic reduction of 4-nitrophenol. Moreover, the composite woods are facile to regenerate and possess superior reusability and stability.
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Catalysts
·
2026
·Vol. 16
·期 9
·807
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IF 4.5
Fukun Bi,Rong Qiao,Jiahao Xu,Yuzhe Lu,Jiafeng Wei,Yaofei Zhang,Xiaodong Zhang
The development of highly efficient catalysts is important for the photothermal catalytic oxidation of volatile organic compounds (VOCs). Herein, MIL-100(Fe) was used as the sacrificial template to prepare MnFeOxcatalysts with different Mn contents through the impregnation–calcination method, and their performance in photothermal catalytic oxidation of toluene was investigated. The results show that the content of Mn significantly affects the crystal phase structure, pore properties, surface chemical state, and optical response of the catalyst. Among them, 30%MnFeOxexhibits the best photothermal catalytic activity, with T50and T90being 211 and 237 °C, respectively, which are significantly lower than those of FeOx(232 and 260 °C). Characterization results suggested that the introduction of Mn caused the bandgap of FeOxto decrease from 1.96 to 1.67 eV. Meanwhile, the surface Fe2+, adsorbed oxygen (Oads) species, and oxygen vacancies were increased, enhancing visible light absorption and gaseous oxygen species adsorption and activation, which promoted the photothermal catalytic oxidation of toluene. Additionally, the 30%MnFeOxcatalyst presented good thermal stability and water resistance. Furthermore, during the reaction process, the in situ activation of the catalyst’s surface induced the increase in surface Fe2+, Mn3+,and Oadsspecies, which enhances the photothermal catalytic activity of the catalyst. Importantly, the in situ DRIFTS results further indicate that toluene is mainly oxidized along the path of toluene → benzyl alcohol → benzoate → maleic anhydride → CO2and H2O. This work provides a theoretical basis for the construction of low-cost, non-precious-metal Mn–Fe-based photothermal catalysts.
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FOOD CHEMISTRY
·
2025
·
IF 9.8
Shan Huang,Danyu Lv,Yuhuan Geng,Fuhao Yue,Xinan Zeng,Mengwai Woo,Zhong Han,Ji Ma
Malachite green (MG) is a toxic contaminant commonly found in aquaculture, making its effective removal and detection crucially important. In this study, MIL-100(Fe) was synthesized via a microwave-assisted hydrothermal method under optimized conditions (150 °C, 200 W, 30 min; FeCl₃·6H 2 O:H₃BTC = 2:3). The resulting material exhibited excellent structural stability, a high specific surface area (1169.9 m 2 /g), and a remarkable MG adsorption capacity of 714.29 mg/g. To enable practical application and reusability, MIL-100(Fe) was immobilized onto a melamine sponge (MeS) using polyvinylidene fluoride (PVDF) as binding agent, forming a recyclable MeS/PVDF/MOF composite. When applied for solid-phase extraction of MG in conjunction with UV detection, the composite demonstrated high recovery rates (92.1–99.4 %), a low detection limit (2.29 μg/L), and consistent performance with over 80 % recovery after six reuse cycles in both real fish and wastewater samples. This study presents a simple, efficient and sustainable strategy for the adsorption and detection of MG in aquatic food matrices.
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Yeshuang Wang,Mingxian Duan,Zhelin Su,Chao Yang,Bingning Wang,Jiawei Kou,Huiling Fan
The abundant Fe 3+ Lewis acidic sites and well-developed pore structure endow the Fe-MOFs with great potential for H 2 S catalytic oxidation at room temperature, but their performance is inferior owing to the insufficient redox ability of the Fe 3+ species inherent in frameworks. Herein, an effective protocol was proposed for the first time to remarkably improve the catalytic oxidation performance of MIL-100(Fe) under ambient conditions through the introduction of Fe 2+ coordinatively unsaturated site (CUS) species into the framework. As expected, the sample after modification had a superior H 2 S breakthrough capacity of 267.3 mg S/g, an 18.4-fold increase compared with that without Fe 2+ CUS (14.5 mg S/g). The introduced Fe 2+ species triggered the Fe 3+ /Fe 2+ redox cycle for H 2 S catalytic oxidation by enhancing the oxidative ability of the Fe 3+ CUS intrinsic to the framework. Moreover, the Fe 2+ CUS was also found act as an active site for O 2 activation into O 2 ∙– , which not only provides an additional pathway for H 2 S catalytic oxidation but also accelerates the redox cycling of Fe 3+ /Fe 2+ during the catalytic oxidation process. On the basis of the experimental findings, a plausible catalytic mechanism involving mixed-valence iron sites in MIL-100(Fe) was proposed.
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ACS Omega
·
2024
·
IF 3.7
Boyao Sun,Xuewei Zheng,Xiaoyu Zhang,Huaiyu Zhang,Yang Jiang
Oxaliplatin (Oxa) is a commonly used chemotherapy drug in the treatment of gastric cancer, but its toxic side effects and drug resistance after long-term use have seriously limited its efficacy. Loading chemotherapy drugs with nanomaterials and delivering them to the tumor site are common ways to overcome the above problems. However, nanomaterials as carriers do not have therapeutic functions on their own, and the effect of single chemotherapy is relatively limited, so there is still room for progress in related research. Herein, we construct Oxa@Mil-100(Fe) nanocomposites by loading Oxa with a metal–organic framework (MOF) Mil-100(Fe) with high biocompatibility and a large specific surface area. The pore structure of Mil-100(Fe) is conducive to a large amount of Oxa loading with a drug-loading rate of up to 27.2%. Oxa@Mil-100(Fe) is responsive to the tumor microenvironment (TME) and can release Oxa and Fe3+ under external stimulation. On the one hand, Oxa can inhibit the synthesis of DNA and induce the apoptosis of gastric cancer cells. On the other hand, Fe3+ can clear overexpressed glutathione (GSH) in TME and be reduced to Fe2+, inhibiting the activity of glutathione peroxidase 4 (GPX4), leading to the accumulation of intracellular lipid peroxides (LPO), and at the same time releasing a large number of reactive oxygen species (ROS) through the Fenton reaction, inducing ferroptosis in gastric cancer cells. With the combination of apoptosis and ferroptosis, Oxa@Mil-100(Fe) shows a good therapeutic effect, and the killing effect on gastric cancer cells is obvious. In a nude mouse model of subcutaneous tumor transplantation, Oxa@Mil-100(Fe) shows a significant inhibitory effect on tumor growth, with an inhibition rate of nearly 60%. In addition to its excellent antitumor activity, Oxa@Mil-100(Fe) has no obvious toxic or side effects. This study provides a new idea and method for the combined treatment of gastric cancer.
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Analytical Chemistry Letters
·
2026
·
IF 1.6
Hongbo Zhao,Zixuan Wang,Xiaoyan Duan,Lingchun Wei,Ganghui Chu
Estradiol (E2) is a steroid hormone that has garnered widespread global attention as an emerging pollutant due to its potential to cause endocrine disruption in organisms upon concentration changes. This experiment achieves highly efficient detection of estradiol based on screen-printed electrodes (SPEs) and a graphene (GPE)/MIL-100(Fe) composite material. The GPE/MIL- 100(Fe) composite, characterized by a rich porous structure, was synthesized via a hydrothermal method, and the modified electrode was prepared using the drop-coating technique. The GPE/MIL-100(Fe) composite was characterized by SEM, XRD, FTIR, and XPS to confirm its structure, composition, and properties. Cyclic voltammetry (CV), differential pulse voltammetry (DPV), and chronoamperometry (CA) were employed to enable continuous monitoring of estradiol in liquid environments. The modified electrode demonstrated significant electrocatalytic activity, exhibiting high sensitivity within a linear range of 2.0 nmol/ mL to 140 nmol/mL, with a practical detection limit (LOD) of 0.002 μmol/mL. The innovation of this study lies in leveraging the synergistic effect of GPE/MIL-100(Fe) to enhance the detection performance for estradiol. In the detection of actual samples such as urine (spiked recovery rate: 103.3% -110.9%) and pond water (spiked recovery rate: 96.7% -110.0%), clear characteristic peaks and good sensitivity for estradiol were observed.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2026
·Vol. 37
·期 11
·806
·
IF 3.2
Wang Hui,Liu Jun,Chang Meng-Jie,Li Jia,Feng Qing,Jia Bo
The weak light absorption, low charge separation efficiency, and poor recyclability severely restrict the practical application of heterogeneous photo-Fenton catalyst MIL-100(Fe). Herein, we report the synthesis of Fe 3 O 4 @MIL-100(Fe) with tunable structures via hydrothermal growth, using Fe(NO 3 ) 3 ·9H 2 O and H 3 btc as precursors on an Ag/Fe 3 O 4 template. Notably, Fe(NO 3 ) 3 ·9H 2 O serves dual roles: it acts as a precursor for MIL-100(Fe) formation and as an oxidizing agent to remove the Ag template. The microstructure of the resulting catalyst can be precisely regulated by varying the Fe 3⁺ dosage. By optimizing the Fe(NO 3 ) 3 ·9H 2 O dosage, the optimal hollow Fe 3 O 4 /MIL-100(Fe) catalyst is obtained, which exhibits excellent dispersion, a distinct core/shell structure, a larger specific surface area (312.6 m 2 /g), a smaller average pore diameter (4.9298 nm), strong magnetic separability, and superior photo-Fenton degradation performance (95.6% within 30 min). After 4 consecutive cycles, the degradation efficiency toward Rhodamine B (RhB) remains above 90%, demonstrating outstanding cycling stability. Electron spin resonance (ESR) analysis confirms that both ·O 2 ⁻ and ·OH are the dominant reactive oxygen species responsible for the catalytic degradation reactions.
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MICROPOROUS AND MESOPOROUS MATERIALS
·
2023
·
IF 5.2
Ning Gu,Yueyang Xu,Yan Yin,Xuzhao Gao,Yongping Zeng
SO x released from the combustion of sulfur-containing compounds in fuels pollute the environment and have a serious impact on human health. Adsorption desulfurization is an effective and environmentally friendly technique for removing sulfur-containing compounds from fuels. Metal-organic frameworks (MOFs) have high specific surface areas and can be easily modified and functionalized, making them excellent candidates for adsorption desulfurization in fuels. In this work, the precursor MIL-100(Fe)-SA was prepared using the hydrothermal method , and the adsorbent Ni@MIL-100(Fe)-SA was obtained by doping Ni 2+ into the resulting MIL-100(Fe)-SA using the impregnation method. FT-IR, X-ray diffraction, scanning electron microscopy, transmission electron microscopy and nitrogen adsorption-desorption isotherms were used to analyze the samples. The results indicated that Ni 2+ was successfully loaded onto MIL-100(Fe)-SA, and the MOF's structure remained stable. The adsorption performance of benzothiophene and thiophene was evaluated through batch adsorption experiments. The adsorption capacities of Ni@MIL-100(Fe)-SA for thiophene and benzothiophene were 23.68 mg S/g and 49.58 mg S/g, respectively. These observations could be ascribed to the π-complexation interactions between Ni 2+ of the framework and thiophenic compounds. The regeneration experiments demonstrated that the spent 11Ni@MIL-100(Fe)-SA-1.5 reach 86% of the adsorption capacity of fresh adsorbent after four cycles. Additionally, the regenerated adsorbent maintained good crystallinity after recycling.
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ANALYTICAL CHEMISTRY
·
2025
·
IF 6.7
Chengzhuo Yu,Jin Xu,Li Xiong,Yarui Wang,Silong Wang,Fanglan Geng,Zesen Shang,Huasheng Wu,Lixia Zhao,Yawei Wang
Luminol-based chemiluminescence (CL) systems, as a powerful tool for bioanalysis, are limited owing to their weak CL intensity and self-decomposition of the classic oxidant H2O2. Herein, we introduced a new luminol CL enhancer, the natural light-driven photocatalyst MIL-100(Fe)/TiO2, for the selective determination of dopamine (DA). By employing MIL-100(Fe)/TiO2 for the first time as an efficient enhancer, the MIL-100(Fe)/TiO2-luminol CL intensity was 100 times higher than that of the classical H2O2-luminol system. The CL spectrum, UV–vis absorption spectroscopy, radical scavenger experiments, and electron spin resonance spectroscopy were utilized to investigate the possible CL mechanism of the MIL-100(Fe)/TiO2-luminol system. All of the results indicated that MIL-100(Fe)/TiO2 can generate reactive oxygen species under mild natural light, which could react rapidly with the luminol anion radical and result in direct CL emission. The sensitive plate for DA was developed based on its inhibiting effect on CL intensity, and the linear range between CL intensity and DA concentration was 100 nM–1000 μM with a detection limit of 16.7 μM (S/N = 3). This study successfully achieved a stable reactant that can directly trigger the CL of luminol without the need for additional oxidizing agents under mild natural light and offers new possibilities for photoinduced amplification technology.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2024
·
IF 4.9
Shuyu Chen,Zhengkai Wu,Xueying Cheng,Lu Chen,Yunning Chen,Yingna Guo,Changhua Wang,Qingkun Shang
In this work, we used a simple hydrothermal method to in-situ grow Zn 3 In 2 S 6 on MIL-100(Fe) octahedra, and obtained a MIL-100(Fe)@Zn 3 In 2 S 6 Z-scheme heterojunction photocatalyst. We systematically studied its performance in degrading phenol and p-nitrophenol (PNP) under visible light. MIL-ZIS 6 -2 can remove 89.1 % of phenol within 120 min and nearly 100 % of PNP within 60 min. Its photocatalytic activity to the degradation of phenol is 30.7 times and 1.7 times higher than that of MIL-100(Fe) and Zn 3 In 2 S 6 , respectively. And the photocatalytic activity to degrade PNP is 18.2 times and 1.4 times higher than MIL-100(Fe) and Zn 3 In 2 S 6 . Further research was conducted on its band structure and photocatalytic response mechanism through photoelectric performance, ultraviolet photo-electron spectroscopy, and electron spin resonance spectrometer testing. The results showed that the formation of Z-scheme heterojunction not only increased the specific surface area of the composite photocatalyst, enabling it to provide more reaction sites, but also effectively suppressed the recombination of photogenerated holes and electrons, improving the redox ability of the photocatalyst. This work provides a new perspective for constructing efficient Zn 3 In 2 S 6 -based composite photocatalysts and addressing environmental issues.
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RENEWABLE ENERGY
·
2021
·
IF 8.001
Hui Li,Junchi Wang,Xiaoling Ma,Yangyang Wang,Guoning Li,Min Guo,Ping Cui,Wanpeng Lu,Shoujun Zhou,Mingzhi Yu
Solid catalyst loss is inevitable by using the traditional separation methods of centrifugation or filtration. To this end, the carbonized MIL−100(Fe) is used to support ammonium sulfate ((NH 4 ) 2 SO 4 ) for synthesizing magnetic solid acid on the purpose of biodiesel production . Influence of preparation factors of loading amount, activation temperature, and activation time on catalytic activity are initially evaluated. With that, the prepared catalyst (CIS) is comprehensively investigated to obtain the optimal esterification parameters for biodiesel production . Moreover, characterizations of TG, XRD, BET, SEM, EDS, FTIR, py−FTIR, VSM, XPS, and Hammett indicator are conducted to elucidate the structure−function relationship between physicochemical property and catalytic activity . Results indicated the CIS is a superparamagnetism material with the saturated magnetism of 22 emu/g, which could be easily recovered from mixture with external magnet. Furthermore, the maximum conversion of 95.68% is obtained with mild conditions: molar ratio of methanol/oleic acid of 8:1 and catalyst amount of 8 wt% at 70 °C for 2 h. Negligible impact is detected for CIS with presence of 5 wt% water content, even with 20 wt% water content, the conversion of 85.88% is still achieved.
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危险品化学品经营许可证（带存储）