JOURNAL OF MATERIALS CHEMISTRY
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2012
·Vol. 22
·期 15
·7449-7455
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IF 5.968
Shu-Hui Huo,Xiu-Ping Yan
The adsorption of malachite green from aqueous solution on a highly porous metal–organic framework MIL-100(Fe) was studied in view of the adsorption isotherm, thermodynamics, kinetics, and regeneration of the sorbent. The adsorption isotherms of malachite green on MIL-100(Fe) followed the Freundlich model, and MIL-100(Fe) possessed heterogeneous surface caused by the presence of different functional groups on the surface. The adsorption of malachite green on MIL-100(Fe) is controlled by an entropy effect rather than an enthalpy change, and obeyed a pseudo-second-order kinetics. Analysis of the intraparticle diffusion plots revealed that more than one process affected the adsorption, and film (boundary layer) diffusion controlled the adsorption rate at the beginning. Evidence from zeta potential and X-ray photoelectron spectroscopic data showed that the adsorption of malachite green was also driven by electrostatic attraction and the interaction between the Lewis base –N(CH3)2 in malachite green and the water molecule coordinated metal sites of MIL-100(Fe). MIL-100(Fe) gave much higher adsorption capacity for malachite green than other conventional adsorbents such as activated carbon and natural zeolite. The high adsorption capacity, good solvent stability, and excellent reusability make MIL-100(Fe) attractive for the removal of MG from aqueous solution.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2020
·
IF 3.573
Yanshu Luo,Bingqiong Tan,Xianghui Liang,Shuangfeng Wang,Xuenong Gao,Zhengguo Zhang,Yutang Fang
MIL-100(Fe) has been proven to have good hydrothermal stability and high vapor uptake and is considered as a promising dehumidification material. However, reduction of the production cost and assembly of the adsorbent and glass fiber paper substrate into the MIL-100(Fe) monolith are challenging. This work presented a dry gel conversion strategy for the rapid synthesis of the MIL-100(Fe) monolith at low temperatures. The porosity and crystalline phase of the products obtained under different crystallization temperatures and times were carefully studied. XRD and SEM characterization indicated that the MIL-100(Fe) crystal could be conveniently synthesized on the substrate at a low temperature of 50–70 °C and in a short time of 2–6 h. The spherical particles assembled from crystals dispersed evenly and tightly on the glass fiber paper. The synthesized MIL-100(Fe) monolith had a thickness of about 270 μm and a MIL-100(Fe) loading of 77.7%. Dynamic and static water vapor adsorption tests revealed that the monolithic adsorbent obtained at 50 °C for 6 h had the largest vapor saturation adsorption capacity (0.581 g/g) and the fastest adsorption rate. Moreover, the monolith owned a low regeneration temperature (below 80 °C) and a satisfactory cycle stability. Convenient equipment, mild synthetic conditions, low renewable energy consumption, and good performance will promote its application in the rotary dehumidification system.
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NEW JOURNAL OF CHEMISTRY
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2021
·Vol. 46
·期 2
·739-746
·
IF 3.591
Tao Wang,Xiqing Liu,Mei Liu,Runhua Liao,Hongquan Zhan,Xiaoxue Qi,Yongqing Wang,Yanju Huang
Black TiO2 and metal–organic frameworks (MOF) are great materials with light-harvesting ability, redox power and consequently catalytic activity. Here, the integration of MIL-100(Fe) with TiO2(B) composite was designed for photocatalytic application, which greatly promoted light-harvesting and charge transfer. As expected, the integrated TiO2(B)/MIL-100(Fe) composite showed high photocatalytic activity due to unique Fe–O–Ti bonds that were constructed, which acted as an electronic tunnel to reduce electronic transfer resistance between MIL-100(Fe) and TiO2(B). In addition, the presence of Fe–O clusters in MIL-100(Fe) can also promote the charge dissociation and improve catalytic activity via the Fe3+/Fe2+ redox cycle. This achievement would help us to understand and design charge transfer pathways in the integration of MOF/semiconductor photocatalysts.
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INDOOR AND BUILT ENVIRONMENT
·
2025
·
IF 2.9
Pengfei Zhang,Wenjian Han,Bo Zhou,Haiqian Zhao
The metal-organic framework MIL-100(Fe) is a novel humidity-regulating material, but it has poor water vapour desorption performance. To address this issue, MIL-100(Fe) was modified using 20% lithium chloride (LiCl), forming stable coordination bonds through ion-dipole interactions. These bonds attract water molecules, enhancing the adsorption capacity and improving the structural stability of the material. After modification, its moisture capacity was increased by 2.42 times, and the desorption amount was increased by 7.22 times, with an overall improvement in moisture adsorption–desorption equilibrium. However, the use of inorganic salts presents a leakage problem in high-humidity environments. To counter this, a 3% ethyl cellulose (EC) coating was applied to the modified MIL-100(Fe). Through surface interactions, this modification improved the material's adsorption performance in non-polar environments, preventing deliquescence in long-term high-humidity conditions. The hydrophobic angle of the modified composite material reached 93°, making the surface hydrophobic. The moisture capacity of the composite material was 1.83 times that of the pure MOF, and the desorption amount was increased by 5.2 times, significantly enhancing the material's environmental humidity regulation performance. Additionally, the material demonstrated good reusability, extending its lifespan, making it suitable for use as an intelligent humidity control material in construction.
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RSC Advances
·
2017
·Vol. 7
·期 5
·2943-2952
·
IF 3.108
Jia Yang,Xiaojun Niu,Shaorong An,Weiyi Chen,Jie Wang,Wei Liu
A novel Bi2MoO6–MIL-100(Fe) heterostructure photocatalyst was synthesized by a facile solvothermal method for the first time, and characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, UV-vis diffuse reflectance spectra, transmission electron microscopy, and photoluminescence spectra. The as-prepared Bi2MoO6–MIL-100(Fe) composites exhibited excellent photocatalytic activity and stability towards the degradation of Rhodamine B (RhB) under visible light irradiation. The introduction of MIL-100(Fe) into semiconductor Bi2MoO6 improved the photocatalytic performance remarkably, and the optimal composite with 9% MIL-100(Fe) content showed the highest photocatalytic activity. According to the active radical trapping experiments, the h+ and ˙O2− radicals were the two main active species in the photocatalytic reaction. The enhanced photocatalytic performance is mainly attributed to the formation of the Bi2MoO6–MIL-100(Fe) heterostructure, which is beneficial to the transfer and separation of photo-generated electron–hole pairs. The possible mechanism of the enhanced photocatalytic performance of the Bi2MoO6–MIL-100(Fe) composites was discussed.
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FIBERS AND POLYMERS
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2021
·Vol. 22
·期 2
·345-353
·
IF 2.153
Liu Jun,Sun Meng,Chang Meng-Jie,Fan Si-Meng,Hui Qian,Ni Fu-Rong,Yuan Bin
Novel CoFe 2 O 4 /MIL-100(Fe) (CFO/MIL-100(Fe)) core/shell nanofibers were prepared by successive ionic layer adsorption and reaction (SILAR) assembly of MIL-100(Fe) on electrospun CoFe 2 O 4 nanofibers. The MIL-100(Fe) shells were constructed on the dispersed CoFe 2 O 4 fiber surface with high uniformity, homogeneous thickness and high stability. Due to the inherent porosity of MIL-100(Fe), a higher specific surface area of 225.77 m 2 /g is achieved for the CFO/MIL-100(Fe)-10 sample. The formed CFO/MIL-100(Fe) catalysts exhibit high catalytic activity towards degradation of rhodamine B (RhB) under visible light irradiation. The photocatalytic activity remains above 77 % within 60 min illumination after four cycles. Due to the simple synthetic method, highly uniform structure, strong magnetic recoverable, as well as good photocatalytic performance, the obtained CFO/MIL-100(Fe) core/shell nanofibers could be promising photocatalysts for practical application.
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ANALYTICA CHIMICA ACTA
·
2026
·
IF 6.1
Peng Zhao,Kai Liu,Yueyan Li,Xiaofang Ban,Yuheng Wu,Jiaqi Liu,Xiaohong Wu,Ziyi Cheng,Fan Wang,Shuo Li,Feng Lin,Huifang Tang,Qingnan Zhao
The excessive activation of sympathetic nerve is closely related to cardiovascular diseases (CVDs). In this study, we developed a novel MIL-100(Fe)@Ag surface-enhanced Raman scattering (SERS) substrate for the simultaneous and effective detection of plasma norepinephrine (NE) and adenosine—two pivotal sympathetic hormones. The microscopic morphology and crystal structure of the substrate were characterized using techniques such as transmission electron microscope (TEM) and X-ray diffraction (XRD). Mechanistically, the HOMO-LUMO energy levels of the detection molecules were calculated using Gaussian. The substrate realized a dual SERS enhancement mechanism through the synergistic effect of localized surface plasmon resonance and interfacial charge transfer. Consequently, the MIL-100(Fe)@Ag platform exhibited high-sensitivity quantitative detection capabilities for NE and adenosine: the detection limit for NE is 0.596 nmol/L; the detection limit for adenosine is 0.24 nmol/L. Crucially, when applied to patients with pheochromocytoma—a neuroendocrine tumor characterized by plasma catecholamine surges, this method achieved robust and stable detection of plasma NE. It offered comparable diagnostic accuracy to conventional mass spectrometry while significantly reducing analysis complexity. Therefore, this innovative strategy may hold great promise for the long-term, decentralized monitoring of sympathetic nerve activity in populations at risk for CVDs or related clinical disorders.
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FUEL
·
2022
·
IF 8.035
Hui Li,Tianyu Wang,Yangyang Wang,Fengsheng Liu,Yan Li,Yunpu Wang,Min Guo,Guoning Li,Xiaoling Ma
Sulfated metal oxides are widely used in catalyzing esterification for biodiesel production due to their low corrosivity and easy separation. While, the catalytic stability is still a challenge on account of active site leaching during successive batch experiments. To this end, the typical metal organic frameworks, MIL-100(Fe) doped with Co was adopted to load ammonium sulfate ((NH 4 ) 2 SO 4 ) for stable heterogeneous acid preparation, which was employed to catalyze the esterification of methanol and oleic acid. Influence of preparation factors of (NH 4 ) 2 SO 4 loading amount and activation temperature on catalytic activity were initially evaluated. Furthermore, to elucidate the effect of Co doping, catalysts were characterized by TG, XRD, FTIR, nitrogen adsorption–desorption, Py-FTIR, XPS, SEM and NH 3 -TPD. Results indicated that the maximum esterification conversion of 92.56 % was achieved by MS(Fe/Co) with molar ratio of methanol to oleic acid of 8:1 and catalyst amount of 8 wt% at 70 °C in 2 h. In comparison to MS(Fe), Co doping significantly improved the stability, where the catalytic activity of MS(Fe/Co) was increased by 20 % at the fifth cycle. The activation energy and pre-exponential factor of esterification catalyzed by MS(Fe/Co) were also calculated as 42.06 kJ/mol and 5.24 × 10 5 min −1 . This study provides a feasible way to enhance the catalytic stability of heterogeneous acid for biodiesel production.
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NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 10
·4806-4813
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IF 3.925
Jie Song,Leilei Sun,Hongchao Geng,Wenlong Tan,Deshuai Zhen,Qingyun Cai
β-Phase NaYF4:Yb,Tm,Gd up-conversion nanorods (UCNRs) with high uniformity were synthesized by a solvothermal method. The optimal fluorescence intensity of UCNRs was explored. After further modification with Materials of Institute Lavoisier-100(Fe) (MIL-100(Fe)) by the layer-by-layer self-assembly method, near-infrared light-triggered UCNR@MIL-100(Fe) nanomaterials with excellent antibacterial performances were constructed. A core–shell structure was constructed and confirmed by transmission electron microscopy (TEM). Reactive oxidizing species (ROS) detection indicated that the nanomaterials owned good photodynamic efficacy. The antibacterial experiments showed that the nanomaterials with 980 nm light irradiation and hydrogen peroxide (H2O2) had good antibacterial activity against Gram-negative and Gram-positive bacteria. Under 980 nm laser excitation, UCNRs generated ultraviolet and visible light to activate MIL-100(Fe) and induced a photo-Fenton reaction, which further produced oxygen species for antibacterial applications.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2021
·
IF 5.816
Chengbao Liu,Dongchen Shen,Zhengkai Tu,Song Li
Li + doping is regarded as an effective strategy to enhance the room-temperature hydrogen storage of metal-organic frameworks (MOFs). In this work, Li + is doped into both MIL-100(Fe) and MIL-100(Fe)/graphene oxide (GO) composite, and it is demonstrated that the hydrogen uptake of Li + doped MIL-100(Fe)/GO (2.02 wt%) is improved by 135% compared with Li + doped MIL-100(Fe) (0.86 wt%) at 298 K and 50 bar, which is ascribed to its higher isosteric heat of adsorption (7.33 kJ/mol) resulting from its more accessible adsorption sites provided by doped Li + ions and ultramicropores. Grand canonical Monte Carlo (GCMC) simulation reveals that Li + ions distributing in the interface between MIL-100(Fe) and GO within MIL-100(Fe)/GO composite is favorable for hydrogen adsorption owing to the increased number of adsorption sites, thus contributing to the enhanced hydrogen storage capacity. These findings demonstrate that MIL-100(Fe)/GO is a more promising Li + doping substrate than MIL-100(Fe).
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2021
·
IF 4.539
Weifeng Li,Tao Zhang,Li Lv,Yanxiao Chen,Wenxiang Tang,Shengwei Tang
A novel strategy of room-temperature synthesis of MIL-100(Fe) with organic amine as deprotonating agent was proposed. The as-prepared solid product was denoted as R-MIL-100(Fe). The material was systematically characterized via XRD , FT-IR, XPS and SEM. The effects of operation parameters such as initial fluoride concentration, reaction time, initial pH and co-existing anions on the fluoride adsorption performance of the synthesized R-MIL-100(Fe) were studied. The maximum fluoride adsorption capacity of R-MIL-100(Fe) was as high as 23.53 mg/g at 298 K in the fluoride solution. The results indicate that the adsorption process of fluorine on R-MIL-100(Fe) belongs to surface adsorption and intraparticle diffusion . An excellent fluoride adsorption performance of R-MIL-100(Fe) was observed in a wide pH range of 4–10. The co-existing anions including Cl - , NO 3 - and SO 4 2- almost had no negative effects on the adsorption performance of R-MIL-100(Fe). However, the present of CO 3 2- or HCO 3 - brought an obvious reduction of F - adsorption capacity of R-MIL-100(Fe). Thermodynamic study results illustrate that the adsorption process was an exothermic chemisorption . Chemical combination of iron and fluorine was confirmed by FT-IR and XPS. The strong combination brings the excellent F - adsorption performance of MIL-100(Fe). R-MIL-100(Fe) was successfully regenerated and recycled five cycles with an excellent regeneration ability and recyclability.
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NEW JOURNAL OF CHEMISTRY
·
2019
·Vol. 43
·期 24
·9725-9731
·
IF 3.069
Suresh Mutyala,Sobhy M. Yakout,Shebl S. Ibrahim,Madhavi Jonnalagadda,Harisekhar Mitta
Iron metal–organic framework, MIL-100(Fe) was prepared by a hydrothermal method and used as a support to incorporate diethylenetriamine (DETA) for the study of CO2 adsorption and separation of CO2/N2. All synthesized adsorbents were characterized by PXRD, N2 adsorption–desorption isotherms, FT-IR, TGA, SEM, and elemental analysis. Structural characterization results have revealed that the structure of MIL-100(Fe) was not changed by the incorporation of diethylenetriamine. The CO2 adsorption capacities were 29 cm3 g−1 and 41 cm3 g−1 at 298 K, 1 bar for MIL-100(Fe) and DETA–MIL-100(Fe), respectively. Adsorption of CO2 on DETA–MIL-100(Fe) was higher than that on MIL-100(Fe). The enhancement was due to the presence of amine groups which could form ammonium carbamate by interaction with CO2. Similarly, the N2 adsorption capacities were 3 cm3 g−1 and 0.9 cm3 g−1 at 298 K, 1 bar for MIL-100(Fe) and DETA–MIL-100(Fe), respectively. The decrease in N2 adsorption capacity was due to the decrease in surface area. The selectivity of CO2/N2 on DETA–MIL-100(Fe) was four times higher than that on MIL-100(Fe). The heat of CO2 adsorption was 74.2 kJ mol−1 at low coverage of CO2 on DETA–MIL-100(Fe) and the CO2 adsorption capacity was constant in each adsorption cycle over the same adsorbent.
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