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CATALYSIS COMMUNICATIONS · 2017 · IF 3.33

Sandwich-like MIL-100(Fe)@Pt@MIL-100(Fe) nanoparticles for catalytic hydrogenation of 4-nitrophenol

Zhiming Chen,Bo Xu,Xiaomei Wang,Li Zhang,Xiaoqing Yang,Cuncheng Li

Separation and recycling of noble metal nanoparticles after catalytic reaction is critical to promote its application efficiency and cut down the cost. This work presents a facile synthesis strategy for the fabrication of sandwich-like MIL-100(Fe)@Pt@MIL-100(Fe) (denoted as S-Pt) nanoparticles with high stability and improved catalytic activity for hydrogenation of nitrophenol. MIL-100(Fe) acts as both carrier to make the catalyst easily separated and shield to protect the tiny Pt nanoparticles from leaching or aggregation during reaction. Moreover, mass transfer effect of the porous MIL-100(Fe) with its pore structure serving as nano-reactor is also benefit for promoting the catalytic efficiency.

CAS / MDL: 10060-10-3 554-95-0
研究领域: 材料科学 · 催化化学
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Enhanced photocatalytic nitrogen fixation on Cu2O clusters/MIL-100(Fe) heterojunction

Xingxing Huang,Yingzhang Shi,Cheng Liu,Zhiwen Wang,Jinhong Bi,Jimmy C. Yu,Ling Wu

A series of Cu 2 O clusters/MIL-100(Fe) heterojunctions with different Cu 2 O mass ratios were constructed as the photocatalysts for N 2 fixation. An optimal nitrogen fixation performance of 51.22 μmol·g −1 ·h −1 is achieved when the mass fraction of Cu 2 O is 20 %. Isotope analysis experiments confirmed that the nitrogen source is N 2 . Possible intermediate signals during photocatalytic reactions were detected by in situ DRIFTS. XPS results further confirm the formation of Cu 2 O/MIL-100(Fe) heterojunctions, and that the existence of Cu–O surface interactions is the key to efficient electron transfer. It is revealed that the improvement of the catalytic performance is derived from the formation of heterojunction which regulates the energy band structure as well as promotes the separation of photogenerated electron-hole pairs. This study proposes a possible mechanism of photocatalytic nitrogen fixation and emphasizes the role of surface interaction and electron transfer in type-II heterojunction in improving nitrogen fixation performance.

CAS / MDL: 2672-58-4
研究领域: 材料科学 · 环境科学
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ANALYTICAL CHEMISTRY · 2025 · IF 6.7

Enhanced Chemiluminescence Induced by Natural Light-Driven MIL-100(Fe)/TiO2 for Dopamine Detection

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.

CAS / MDL: 98-00-0 144-55-8 51-61-6
研究领域: 分析化学 · 生物医学工程
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CATALYSIS COMMUNICATIONS · 2017 · IF 3.33

Glycol assisted synthesis of MIL-100(Fe) nanospheres for photocatalytic oxidation of benzene to phenol

Bo Xu,Zhiming Chen,Bing Han,Cuncheng Li

This work presents MIL-100(Fe) nanoparticles synthesized using glycol with uniform size and morphology. This is the first report of nanoscale MOFs material synthesized using glycol. The MIL-100(Fe) particles have been characterized by SEM, TEM, XRD and the results indicate that the MOFs particles show monodispersed nanospherical morphology. Photocatalytic study reveals that the MIL-100(Fe) nanospheres exhibit good oxidation ability of benzene to phenol under visible light irradiation with high selectivity.

CAS / MDL: 10060-10-3 554-95-0
研究领域: 材料科学 · 环境科学 · 化学工程
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MICROPOROUS AND MESOPOROUS MATERIALS · 2022 · IF 5.876

Delignified wood supported MIL-100 (Fe) for fast adsorption removal of tetracycline

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.

研究领域: 环境科学 · 材料科学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2014 ·Vol. 22 ·期 5 ·3856-3864 · IF 2.757

Solubilization of 4,4′-dibromodiphenyl ether under combined TX-100 and cosolvents

Yang Xingjian,Lu Guining,Wang Rui,Guo Chuling,Zhang Hongliang,Dang Zhi

This paper is focused on the selection of cosolvents in the remediation of contaminated soils. The aim of this study was to investigate the combined effects of Triton X-100 (TX-100) and different cosolvents on the solubilization behavior of 4,4′-dibromodiphenyl ether (BDE-15) and the washing of BDE-15 from a contaminated soil. 1 H NMR spectroscopies were used to elucidate the interactions among TX-100, cosolvents, and BDE-15 in aqueous micellar solution. Results showed that the solubility of BDE-15 was enhanced by the observed synergism among TX-100, BDE-15, and cosolvents, and the TX-100/dimethyl sulfoxide (DMSO) system exhibited the best performance in the solubilization of BDE-15. Similar synergism was further evidenced in the washing of BDE-15 from a contaminated soil. With 10 % ( v / v ) DMSO and 6.4 mM TX-100 solution added, considerable synergistic effect was achieved in TX-100/DMSO system, leading to the highest removal efficiency (92.9 %) of BDE-15 from the soil, relative to that of 67.3 % with TX-100 alone at the same concentration.

CAS / MDL: 111689-03-3
研究领域: 环境科学 · 化学
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DALTON TRANSACTIONS · 2025 ·Vol. 54 ·期 8 ·3467-3477 · IF 3.3

TiO2/CoOx heterostructure decorated MIL-100(Fe) by atomic layer deposition for enhanced photocatalytic oxygen production

Wenhui Hu,Zhongxin Song,Lingna Sun,Lei Zhang,Qianling Zhang,Xiangzhong Ren,Yongliang Li

Efficient separation of photogenerated charge carriers is essential for maximizing the photocatalytic efficiency of semiconductor materials in oxygen evolution reactions (OER). This study presents a novel trimetallic photocatalyst, MIL-100(Fe)/TiO2/CoOx, synthesized through a facile microwave-assisted hydrothermal method followed by atomic layer deposition (ALD). The porous MIL-100(Fe) serves as a support for the sequential deposition of TiO2 and CoOx layers via ALD, which enhances electron–hole pair separation and minimizes their recombination. Characterization using transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) confirms the uniform deposition of TiO2 and CoOx layers on the MIL-100(Fe) surface. The optimized photocatalyst, processed with 20 deposition cycles of Co, exhibits exceptional photocatalytic OER performance, with an oxygen evolution rate of 558.3 μmol g−1 h−1. This enhancement in activity is attributed to the synergistic interaction between the spatially separated TiO2 and CoOx cocatalysts, which facilitates efficient charge transfer and increases the number of active sites. These findings highlight the potential of ALD-fabricated heterostructures in the development of advanced photocatalysts for sustainable energy production.

CAS / MDL: 7439-89-6
研究领域: 材料科学 · 能源化学
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SENSORS AND ACTUATORS B-CHEMICAL · 2024 · IF 8

Ultra-sensitive electrochemiluminescence monitoring of microRNA via Triton X-100 functionalized carbon dots-based nanocomposites

Yuqin Yang,Gui Zhang,Li Song,Guangrong Kuang,Yilan Ding,Shuchun Bu,Yaqin Chai,Yingzi Fu

Carbon dots (CDs) with excellent optical performance have attracted tremendous interest for the construction of electrochemiluminescence (ECL) biosensors. However, the intrinsic self-aggregation behavior of CDs brings a serious issue of aggregation-caused quenching (ACQ), which can quench the ECL emission. In this work, different surfactants (non-ionic, anionic and cationic) were used to modulate the preparation of functionalized CDs (CDs-based nanocomposites). Their ECL performances were significantly enhanced in potassium persulfate solution. In particular, the highest ECL intensity obtained from the Triton X-100 functionalized CDs (T-CDs) was 16.8-fold than that of CDs as ACQ was suppressed effectively. Therefore, utilizing T-CDs as an ECL luminophore, integrating with the catalytic hairpin assembly and strand displacement reaction signal amplification strategies, a "Signal on" ECL biosensor was constructed for microRNA-21 (miRNA-21) monitoring. The proposed biosensor shows a dynamic range from10 fmol·L −1 to 10 nmol·L −1 at a low detection limit of 2.9 fmol·L −1 (S/N = 3). Meanwhile, it exhibits good results for analyzing miRNA-21 in healthy human samples and the expression in MCF-7 and HeLa cells. This work not only expands the method for suppressing ACQ of CDs, but also shows great potential for the analysis of other biomarkers by replacing the corresponding DNA sequences , so as to realize the early diagnosis.

研究领域: 生物传感技术 · 分子诊断学 · 纳米生物学
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ENVIRONMENTAL POLLUTION · 2019 · IF 5.714

Mechanistic insight into the adsorption of diclofenac by MIL-100: Experiments and theoretical calculations

Shuting Zhuang,Yong Liu,Jianlong Wang

The development of high-efficiency adsorbents and the exploration of their adsorption mechanisms are major challenges in environmental remediation. Herein, MIL-100 was prepared, characterized, and utilized for the adsorptive removal of diclofenac sodium (DCF) from aqueous solutions. A high monolayer adsorption capacity of 773 mg g −1 was recorded. The adsorption mechanism was proposed based on different contributions of two types of pore structure of MIL-100 to the adsorption of DCF from aqueous solutions according to the experimental results and theoretical calculation. During adsorption process, DCF (5.2 × 7.4 × 10.3 Å) diffused through the free area of hexagonal pores (8.6 × 8.6 Å) into the cages of MIL-100, whilst it was adsorbed by the pentagonal pores (4.8 × 5.8 Å) preferentially. Internal mass transfer resistance, which was identified as one of the dominant rate-limiting steps by the mass transfer resistance kinetic models based on the Sips model, will be derived from the diffusion process, which was affected by the size-sieving effect of the pore structure of MIL-100. The successful diffusion of DCF into the interior of MIL-100 and the stable configuration between MIL-100 and DCF accounted for the high adsorption capacity. The capture of DCF into MIL-100 also resulted in the pore size distribution variation of adsorbent, which provided vital experimental evidence for the proposed mechanism. This study may offer deeper insights into other pollutants removal by metal-organic frameworks type adsorbents.

研究领域: 环境科学 · 材料科学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Efficient photocatalytic degradation of phenolic pollutants using MIL-100(Fe)@Zn3In2S6 Z-scheme heterojunction

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.

研究领域: 材料科学 · 环境科学
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ENGINEERING IN LIFE SCIENCES · 2012 ·Vol. 13 ·期 2 ·194-200 · IF 1.925

Immobilization of cellulases on the reversibly soluble polymer Eudragit S-100 for cotton treatment

Yuanyuan Yu,Jiugang Yuan,Qiang Wang,Xuerong Fan,Ping Wang,Xuejiao Sun

Cellulases can penetrate into the fiber, causing tensile strength loss of the cellulosic fibers or fabrics. To minimize the tensile strength loss, we have immobilized cellulases on Eudragit S-100. The characteristics of covalent Eudragit cellulase were evaluated using gel filtration analysis and UV spectra. Gel filtration analysis revealed that the cellulases were covalently bound to the polymer. Covalent Eudragit cellulase was loaded with the enzyme of about 40% and had a relative activity about 80% at a Eudragit S-100 concentration of 15 g/L. When cellulase is bound to the polymer, the solubility profile becomes similar to the one of Eudragit. In addition, the effects of the enzyme on the cotton yarns and fabric using cellulases have been investigated. Native and immobilized cellulases caused improvements in whiteness and wrinkle recovery angle of the fabric in comparison to the control samples. The bending stiffness results show that native and immobilized cellulase treated cotton fabric has an improved softness than the control samples. It was found that using the immobilized cellulase reduced the weight and tensile strength, because the hydrolytic attack is only limited to the surfaces of cotton fibers.

研究领域: 生物化学 · 纺织科学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2023 · IF 5.2

Synergistic desulfurization over Ni(II) and Fe sites in adsorbent Ni@MIL-100(Fe)

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.

研究领域: 材料科学 · 环境科学
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