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MATERIALS CHEMISTRY AND PHYSICS · 2020 · IF 3.408

Influence of microwave-assisted synthesis on the structural and textural properties of mesoporous MIL-101(Fe) and NH2-MIL-101(Fe) for enhanced tetracycline adsorption

Yanan Dong,Tianding Hu,Manoj Pudukudy,Hongying Su,Lihong Jiang,Shaoyun Shan,Qingming Jia

In this paper, the effect of conventional solvothermal and a microwave-assisted method for the synthesis of MIL-101(Fe) and NH 2 -MIL-101(Fe) as adsorbents for the removal of tetracycline in wastewater is reported for the first time. The results had shown that the microwave treatment led to a significant reduction in the material synthesis time, which greatly saved the energy. It was also found that the microwave-assisted synthesized material exhibited small particle size, high specific surface area and better adsorption capacity. The introduction of amino group further enhanced the adsorption capacity of MIL-101(Fe). The adsorption capacity of MIL-101(Fe) and NH 2 -MIL-101(Fe) samples for tetracycline adsorption by microwave assisted synthesis method reached up to 332 mg/g and 378 mg/g, respectively. Moreover, the adsorption isotherm was well-fit with Freundlich model, indicating a multilayer adsorption . The kinetic studies indicated that the reaction followed pseudo second-order reaction kinetics with a best fit to the theoretical value. Due to the higher adsorption efficiency and lower energy consumption of the synthesis, the as-prepared microwave assisted materials could be used as potential adsorbents for different pollutants in wastewater.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

Green fabrication of highly flame-retardant, anti-ultraviolet radiation and superhydrophobic cellulose-based fabric by constructing dualtielement-containing NH2-MIL-53(Al)@Triethoxyoctylsilane nano coatings

Jiang Chang,Ying Qin,Weimin Guo,Jingyuan Zhang,Kuo Zhang,Jianhua Zheng,Lijian Sun,Qiu Fu

The facile and eco-friendly fabrication of a fabric with remarkable flame retardancy, anti-ultraviolet (UV), and superhydrophobic properties is of significant interest for multitask requirements. In this regard, herein, a nonfluorine, facile, and green method is reported for in situ synthesis of metal-organic frame (NH 2 -MIL-53(Al)) on hemp fabric (HF) for the preparation of multifunctional textiles. A homogeneous and compact coating of NH 2 -MIL-53(Al) crystals was deposited on HF, followed by modification with triethoxyoctylsilane (TEOS) to manufacture superhydrophobic NH 2 -MIL-53(Al)@hemp fabric (SM(Al)HF-9), significantly enhancing its water stability. The SM(Al)HF-9 exhibited superior superhydrophobicity properties, with a water contact angle (WCA) up to 156°. Furthermore, the surface of SM(Al)HF-9 cannot be adhered by dye solution and powder, indicating its good self-cleaning and anti-fouling abilities. The SM(Al)HF-9, characterized by a porous structure, effectively separates tetrachloromethane and n-hexane from water mixtures with a separation efficiency exceeding 97 %. The SM(Al)HF-9 has excellent UV-blocking properties, and the UV protection factor is as high as 105.44. Encouragingly, the SM(Al)HF-9 exhibited outstanding flame retardancy, as demonstrated by its self-extinguishing capability and a substantially improved limiting oxygen index (LOI) of 32.4 %. In comparison to raw HF, the peak heat release rate (PHRR) and total heat rate (THR) of the modified HF are reduced by 76.15 % and 54.32 %, respectively. Meanwhile, the NH 2 -MIL-53(Al) has a significant advantage over other MOFs (e.g., ZIF-67, Ce-MOF, Ag-MOF, Fe-MOF and MIL-53(Al)) in improving the flame retardancy of HF. The highly efficient flame-retardant, anti-UV, and superhydrophobic fabric is promising in home and public decoration, and fire protection fields.

CAS / MDL: 7446-70-0
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ENVIRONMENTAL POLLUTION · 2022 · IF 9.988

Versatile crosslinking synthesis of an EDTA-modified UiO-66-NH2/cotton fabric composite for simultaneous capture of heavy metals and dyes and efficient degradation of organophosphate

Yue Gao,Lifeng Yao,Shengzu Zhang,Qinyan Yue,Weiyan Yin

The metal-organic frameworks/cotton fabric composites (MOFs/CFCs) have emerged as a new type of prospective materials for environmental cleanup , due to their convenient recyclability and high removal efficiency towards hazardous pollutants . However, their practical applications are limited by complicated synthetic conditions, insufficient interface bonding and poor adsorption capacity. Herein, for the first time, a robust ethylenediaminetetraacetic acid (EDTA)-functionalized MOFs/CFC is prepared based on UiO-66-NH 2 crystals by using EDTA dianhydride as the cross-linking agent, and applied for simultaneous removal of heavy metals and dyes, as well as degradation of chemical warfare agents. The as-prepared EDTA-UiO-66-NH 2 /CFC shows extraordinary monocomponent adsorption performance with maximum adsorption capacity of 158.7, 126.2, 131.5, 117.4 and 104.5 mg/g for Cd(II), Cu(II), methylene blue , crystal violet and safranin O, respectively. Interestingly, in metal-dyes binary system, the uptake of Cu(II) by EDTA-UiO-66-NH 2 /CFC increases significantly when co-existing high concentration of dyes. The results indicate that the synergistic and simultaneous removal of both dyes and metal from complex systems can be realized by EDTA-UiO-66-NH 2 /CFC via multiple mechanisms. The EDTA-UiO-66-NH 2 /CFC also exhibits an outstanding catalytic performance for degrading dimethyl 4-nitrophenylphosphate. Besides, it can be reused for several times without obvious decrease of its adsorption and catalysis efficiencies. More impressively, the cross-linking reaction approach can not only anchor UiO-66-NH 2 crystals firmly onto cotton fabric, but also facilitate in-situ formation of abundant adsorption sties on the adsorbent surface. Therefore, this work offers a simple and versatile synthetic strategy to develop high-performance environmental material for multiple pollutants remediation.

CAS / MDL: 10312-55-7 10026-11-6
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Separations · 2021 ·Vol. 8 ·期 11 ·196 · IF 2.777

Selective Separation and Analysis of Catecholamines in Urine Based on Magnetic Solid Phase Extraction by Mercaptophenylboronic Acid Functionalized Fe3O4-NH2@Au Magnetic Nanoparticles Coupled with HPLC

Qing Han,Xiaoxiao Wu,Yi Cao,Hua Zhang,Yuqin Zhao,Xuejun Kang,Huaiyuan Zhu

A novel magnetic solid phase extraction based on mercaptophenylboronic acid (MPBA)-functionalized Fe3O4-NH2@Au nanomaterial (Fe3O4-NH2@Au-MPBA) was developed for selective separation and enrichment of catecholamines (including dopamine, norepinephrine and adrenaline). Fe3O4-NH2@Au-MPBA nanoparticles were achieved by self-assembly-anchoring MPBA molecules on the surface of Fe3O4-NH2@Au nanocomposites, which were synthesized via a facial ultrasonic auxiliary in situ reduction process. The interaction between cis-diol from catecholamines and boronic acid was reversible and could be flexibly controlled by adjusting pH value. The catecholamines could be quickly adsorbed by Fe3O4-NH2@Au-MPBA in weak alkaline solution (pH 8.0–9.0) and subsequently released in acid solution (pH 1.0–2.0). The process of adsorption and dissociation was very fast. Furthermore, the three catecholamines could be detected in urine from children by high performance liquid chromatography (HPLC) with electrochemical detector. Under optimal conditions, norepinephrine (NE), epinephrine (EP) and dopamine (DA) were separated very well from internal standard and exhibited a good linearity in the range of 2.5–500.0 ng mL−1, with correlation coefficients of r2> 0.9907. Limits of detection (LOD) (signal to noise = 3) were 0.39, 0.27 and 0.60 ng mL−1for NE, EP and DA, respectively. Recoveries for the spiked catecholamines were in the range of 85.4–105.2% with the relative standard deviation (RSD) < 11.5%.Keywords:Fe3O4-NH2@Au;magnetic solid phase extraction;catecholamines;HPLC;electrochemical detection;urine

CAS / MDL: 16290-26-9
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Reaction Chemistry & Engineering · 2021 ·Vol. 7 ·期 1 ·84-100 · IF 4.239

Facile synthesis of novel NH2-MIL-53(Fe)/AgSCN heterojunction composites as a highly efficient photocatalyst for ciprofloxacin degradation and H2 production under visible-light irradiation

Jungang Yi,Xianghui Wu,Huadong Wu,Jia Guo,Kun Wu,Linfeng Zhang

With the aim of solving the increasingly serious problem of environmental pollution and the energy crisis, in this work a novel NH2-MIL-53(Fe)/AgSCN (NMFA) composite photocatalyst was successfully prepared through a one-step chemical precipitation method. The prepared composites demonstrate an excellent photocatalytic performance for ciprofloxacin (CIP) and rhodamine B (RhB) degradation under visible-light irradiation. Within 60 min, the degradation rate for CIP and RhB reached 90% and 100%, respectively, which was 1.84/3.33 times and 1.79/2.04 times greater than that of the single NH2-MIL-53(Fe) and AgSCN samples. Furthermore, the H2 production rate of the NMFA-5 composite was 4742 μmol g−1 h−1, which was 5.25 and 17.37 times greater than that of the pure samples. Owing to the combination of NH2-MIL-53(Fe) and AgSCN, the separation and transmission efficiency of the photon-generated carriers in the composites was improved, which was demonstrated using optical characterization and a series of electrochemical characterization techniques. In addition, a possible mechanism for the excellent photocatalytic performance of the NMFA composites is discussed. The work in this paper may provide a technical reference for the application of silver modified metal organic frameworks (MOFs)-based composite photocatalysts for the treatment of environmental remediation.

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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Magnetic capture of sulfur quantum dots encapsulated in MOF-5-NH2 via a target-driven self-cycling catalyzed hairpin assembly for the sensitive detection of patulin

Xiaohai Yan,Yuning Zhao,Gengan Du,Qi Guo,Hong Chen,Qian He,Qiannan Zhao,Huanfeng Ye,Jianlong Wang,Yahong Yuan,Tianli Yue

Tools to detect low molecular weight mycotoxin patulin (PAT) are urgently needed because of its harm to human health. Here, we report a simple, effective, and sensitive fluorescent aptasensor based on sulfur quantum dots encapsulated in MOF-5-NH 2 ( [email protected] 2 ) and self-cycling catalyzed hairpin assembly (scCHA) for the detection of PAT in apple juice. The [email protected] 2 synthesized by a “bottle-around-ship” solvothermal method works as a fluorescent probe and offers enhanced fluorescence intensity and good water-solubility versus MOF-5-NH 2 due to the encapsulation of water-soluble SQDs . Meanwhile, the scCHA designed by the two DNA hairpins is initiated after the formation of PAT/aptamer, which further recycles PAT to effectively capture multiple fluorescence probes ( [email protected] 2 ) and amplify the detection signal. Attributed to the synergistic effect between the strong fluorescence intensity of [email protected] 2 and the efficient PAT utilization of scCHA, the fluorescent aptasensor exhibits high sensitivity with detection limits as low as 0.753 pg/mL. The system has satisfactory specificity, anti-interference, and reproducibility (RSDs of intra-assay and inter-assay were 3.24% and 8.60%, respectively). The recoveries in apple juice were between 89.03% and 107.67%, which were with good consistency versus high-performance liquid chromatography (HPLC). These data collectively show that the developed fluorescent aptasensor has a good practical application value.

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JOURNAL OF HAZARDOUS MATERIALS · 2023 · IF 13.6

Self-assembled Fe3O4-NH2 @g-C3N4 composite for magnetic solid-phase extraction of benzophenones in sea water and lake water coupled with LC-MS/MS determination

Man-Man Wang,Zi-Ling Li,Han Wu,Ke-Yan Chen,Fan Guo,Gui-Fu Zuo,Yu He,Xue-Bo Yin

Magnetic solid-phase extraction (MSPE) was developed based on a well-designed Fe 3 O 4 -NH 2 @g-C 3 N 4 nanocomposite as sorbent for a mixture of six benzophenones (BPs) in environmental water samples. The composite fabricated via in-situ self-assembled g-C 3 N 4 shell with homogeneous polymerization of cyanuric chloride and cyanuric acid on Fe 3 O 4 -NH 2 core. While high adsorption capacity was derived from g-C 3 N 4 via hydrophobic, π-π and hydrogen bonding interactions to the targets, the fast magnetic separation was realized with Fe 3 O 4 core for less solvent consumption. In combination with LC-MS/MS, the Fe 3 O 4 -NH 2 @g-C 3 N 4 sorbent minimized the interfering components, reduced the matrix effects, and provided the enrichment factors of 121–150 for six BPs with relative standard deviations ≤ 9.7% even after 20 times extraction-desorption cycles. The present method gave the detection limits of 0.3–2.5 ng/L for six BPs with the linear ranges of 1.0–2000 ng/L, and the recoveries of 84.6%−104% in sea water and 86.2%−107% in lake water samples. Thus, the Fe 3 O 4 -NH 2 @g-C 3 N 4 -based MSPE coupled with LC-MS/MS method provided a convenient, efficient, and reliable alternative to monitor trace BPs in environmental water samples.

CAS / MDL: 131-56-6 127827-52-5
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FOOD CONTROL · 2023 · IF 6

Facile fabrication of Fe3O4@UiO-66-NH2/popcorn-like gold nanoparticles based SERS substrate for selective enrichment and real-time detection of residual enrofloxacin in milk

Yangjie Chen,Li Zheng,Juan Hao,Lijuan Huang,Qinghui Wang,Youting Zhou,Zhihang Yin,Lingpu Jia,Huiming Li,Wenlong Liao,Kunping Liu

In this study, a magnetic metal-organic frameworks (MOFs) based hybrid substrate was designed and fabricated for SERS detection of enrofloxacin (ENR) in milk. The magnetic MOF (Fe 3 O 4 @UiO-66-NH 2 ) was synthesized by a facile microwave-assisted method, then loaded with popcorn-like Au nanoparticles (NPs) through electrostatic interaction. The as-prepared SERS substrate (Fe 3 O 4 @UiO-66-NH 2 /Au NPs) integrated the abundant hot spots of popcorn-like Au NPs with porous Fe 3 O 4 @UiO-66-NH 2 , which greatly improved its SERS activity and stability. More importantly, benefiting from the fingerprint characteristics of SERS and adsorption performance of Fe 3 O 4 @UiO-66-NH 2 , the SERS substrate exhibited high selectivity and sensitivity in detecting ENR. Under the optimal detection condition, a good linearity (R 2  = 0.996) was obtained with ENR concentration of 1.0 × 10 −9 –1.0 × 10 −6  M in spiked milk, the LOD was as low as 5.26 × 10 −10  M, and the recoveries were in the range of 76.1–86.1 % at three different spiking levels. The whole detection process including sample pretreatment took about 50 min, which indicating that the prepared substrate has great potential in sensitive and real-time detection of ENR in milk.

CAS / MDL: 57-09-0 989-38-8
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2023 · IF 22.1

Amino-rich Ag-NWs/NH2-MIL-125(Ti) hybrid heterostructure via LSPR effect for photo-assist uranium extraction from fluorine-containing uranium wastewater without sacrificial agents

Boyuan Tu,Kaifu Yu,Dengjiang Fu,Li Zhou,Ruixiang Wang,Xinying Jiang,Huanhuan Liu,Xin Cao,Xiang Gong,Rong He,Yongjian Tang,Tao Chen,Wenkun Zhu

Photo-assist uranium extraction from fluorine-containing uranium wastewater by building semiconductor-plasma material heterostructure is a forward-looking strategy, which not only effectively accelerates F-U separation via the LSPR effect but also impacts the intensity of binding between U (VI) and site. Here, we developed an amino-rich Ag-NWs/NH 2 -MIL-125(Ti) (AgNW/N-M(Ti)) hybrid nanowires with LSPR effect for photo-assist uranium extraction. Accordingly, the AgNW/N-M(Ti) hybrid nanowires presented 90.4% removal efficiency for U(VI) without a sacrificial agent at the U: F molar ratio of 1:20. By virtue of In-situ KPFM, we identify hot electrons generated over AgNW were transferred to amino-rich N-M(Ti) to efficiently reduce the U(VI) adsorbed on the N-M(Ti), which effectively enhances the excellent uranium removal performance of AgNW/N-M(Ti) hybrid nanowires. This strategy may open a paradigm for the development of advanced heterojunctions with the LSPR effect as catalysts for photo-assisted uranium extraction from fluorine-containing uranium wastewater.

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MATERIALS CHEMISTRY AND PHYSICS · 2023 · IF 4.6

The Fe3O4@UiO-66-NH2/PVDF-co-CTFE mixed matrix membrane with enhanced anti-fouling and self-cleaning performances for effectively removing dyes by Fenton reaction

Xiaoyu Bai,Peng Liu,Xingtong Gao,Kai Liu,Aixiang Li,Zijian Lyu,Qiuhong Li

It is a major obstacle to further development of membrane technology that membrane fouling occurs. In this study, a novel Fe 3 O 4 @UiO-66-NH 2 /PVDF-co-CTFE mixed matrix membrane was successfully developed by mixing Fe 3 O 4 @UiO-66-NH 2 nanoparticles (NPs) into PVDF-co-CTFE membrane through a simple non-solvent-induced phase separation (NIPS) method, and was used for degradation of organic wastewater. The results of the incorporated Fe 3 O 4 @UiO-66-NH 2 NPs content on the morphology, pore structure and physicochemical structure of samples were investigated systematically. The results indicated that the Fe 3 O 4 @UiO-66-NH 2 NPs addition in membrane matrix improved the permeability and significantly enhanced the anti-fouling performance. When 2 wt% Fe 3 O 4 @UiO-66-NH 2 NPs was added, the mixed matrix membrane had excellent comprehensive performance, maintaining a high pure water flux of 226.8 L m −2  h −1 , the BSA rejection rate reached 95.9%, and the flux recovery rate was 71.38%. Importantly, the membrane possessed high catalytic performance based on the Fenton reaction mechanism, and the removal rate of 20 mg L −1 MB solution (400 mL) was up to 99.04%, and showed excellent self-cleaning characteristics and long-term stability. In conclusion, this study provided a new idea for the development of Fenton catalytic membranes with excellent anti-fouling performance for wastewater treatment in complex environments.

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LANGMUIR · 2018 · IF 3.789

Metal–Organic Framework MIL-101-NH2-Supported Acetate-Based Butylimidazolium Ionic Liquid as a Highly Efficient Heterogeneous Catalyst for the Synthesis of 3-Aryl-2-oxazolidinones

S. Y. Chong,T. T. Wang,L. C. Cheng,H. Y. Lv,M. Ji

A novel heterogeneous catalyst, the ionic liquid (IL) of 1-butyl-3-methylimidazolium acetate (BmimOAc) immobilized on MIL-101-NH2, denoted as IL(OAc–)-MIL-101-NH2, was prepared by the “ship-in-a-bottle” strategy. The IL of BmimOAc was prepared in the MIL-101-NH2 nanocages primordially, in which the condensation product of MIL-101-NH2’s amine group with 1,1′-carbonyldiimidazole (CDI) reacted with 1-bromo butane, and then the intermediate exchanged with potassium acetate. The structure and physicochemical properties of IL(OAc–)-MIL-101-NH2 were characterized by powder X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, DRS UV–vis, nitrogen adsorption–desorption, and elemental analysis. The results indicated that BmimOAc was anchored in the MIL-101-NH2 skeleton via the acylamino group and confined in the nanocages in the form of a single molecule. The composite material of IL(OAc–)-MIL-101-NH2 exhibited excellent catalytic activity and catalytically synthesized 3-aryl-2-oxazolone in an excellent yield of 92%. It can be reused up to six times without noteworthy loss of its activity and demonstrated distinct size-selective property for substrates. It was conjectured that the diffusion kinetics of reactants could be controlled by the aperture size of the metal–organic framework support.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2015 · IF 2.729

A sensitive glucose biosensor based on the abundant immobilization of glucose oxidase on hollow Pt nanospheres assembled on graphene oxide–Prussian Blue–PTC-NH2 nanocomposite film

Wailan Xu,Junlin He,Liuliu Gao,Jing Zhang,Junmin Hui,Yanlei Guo,Wenjuan Li,Chao Yu

A simple process in which a graphene oxide (GO)–Prussian Blue (PB)-3,4,9,10-perylenetetracarboxylic dianhydride derivative (PTC-NH 2 ) nanocomposite film is spread onto a glassy carbon electrode (GCE) surface is described. Glucose oxidase (GOD) was adsorbed on the modified glass carbon electrode via the specific structure of hollow Pt nanospheres. This process was sufficient to prevent GOD from leaching away, and to improve the sensitivity of our sensor. To characterise the sensors, several techniques were employed, including transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, cyclic voltammetry (CV), electric impedance spectroscopy (EIS) and chronoamperometry. The resulting amperometric glucose biosensor exhibited a fast response time (within 5   s) and a good linear calibration range from 0.01   ±   0.06   mM to 5.23   ±   0.04   mM with a lower limit of detection of 3.3   μM ( S / N   =   3). Possible interferents, including ascorbic acid, l-cysteine, dopamine and ethanol, showed almost negligible electrochemical responses, indicating the high specificity of the proposed biosensor for glucose detection. The improved performance of the proposed electrode for detecting glucose in human serum was ascribed to the high surface-to-volume ratio and the excellent conductivity of the hollow Pt nanospheres. This skilful strategy of incorporating the GO/PB/PTC-NH 2 nanocomposite film with hollow Pt nanospheres enhances the performance of the electrochemical sensor, which holds promising for application in bioassay analysis.

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