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Uio-66
APPLIED CATALYSIS A-GENERAL · 2024 · IF 4.7

Degradation of emerging pollutant CBZ by a novel hydrogen-promoted Fenton system constructed with Pd/UiO-66(Zr)-2OH

Xin-Hao Shen,Feng Liu,Qin-Qin Chen,Ying Gao,Xiao-Wen Wang,Xin Liu

The efficient degradation of emerging pollutants in water, represented by CBZ, is receiving increasing attention from all sectors of society. Although advanced oxidation reactions represented by Fenton reaction can efficiently degrade emerging pollutants, the problem of iron sludge that comes with it is hindering the further promotion of this technology. Herein, UiO-66(Zr)-2OH material was synthesized by hydrothermal method and loaded with Pd 0 NPs on the surface of the material by in situ reduction. The MOFs-H 2 -Accelerated Catalytic Fenton system was constructed by accelerating the regeneration of Fe(II) in the system by activating the [H] produced by H 2 introduced into the system at room temperature and pressure. Within 180 min, the removal of the target pollutant CZB could reach more than 99 % under the condition of only 25 µmol of Fe(II) and 25 mmol of H 2 O 2 .

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Frontiers of Chemical Science and Engineering · 2025 ·Vol. 19 ·期 4 ·1-11 · IF 4.5

Construction of CS@APP@UiO-66 through self-assembly technology as flame retardant and smoke suppressant for epoxy resins

Shao Siqing,Jin Liping,He Siyuan,Feng Yijing,Guo Wenwen

To achieve fire-resistant epoxy resin (EP), a UiO-66-based novel flame retardant coating (CS@APP@UiO-66) was prepared by modifying UiO-66 with chitosan (CS) and ammonium polyphosphate (APP) through a layer-by-layer (LbL) self-assembly method, which was then introduced into an EP system to improve its fire safety. The results of scanning electron microscopy, X-ray diffraction and Fourier transform infrared spectroscopy show that the unsaturated Zr atoms in the UiO-66 framework provide many active sites conducive to modification, so that the UiO-66 particles, which originally had a regular octahedral structure, are more dispersed by LbL modification without causing doping or distortion issues. The thermogravimetric analysis results indicate that the char residue of EP/2% UiO-66 is increased by 2.52% compared with that of pure EP, indicating that the thermal properties of the EP composite are improved after modification. In addition, the cone test results indicate that EP/2%UiO-66-5L has good flame retardancy and smoke suppression properties, and the peak heat release rate, total smoke production and rate of CO generation values are 25.2%, 5.7% and 38.5% lower than those of the unmodified EP. Moreover, it can be concluded from the Raman test that the graphitization degree of the modified EP composite is strengthened. The above results indicated that after the incorporation of CS@APP@UiO-66 into the EP composites, more char layers formed as physical barriers to prevent the transfer of mass and heat, thus reducing the speed of flame propagation. Therefore, the flame resistance and smoke suppression of the EP composites improved. These favorable characteristics, including high flame retardant efficiency and good smoke suppression, make LbL-functionalized UiO-66 promising for flame retardant polymer applications.

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INDUSTRIAL CROPS AND PRODUCTS · 2024 · IF 5.6

Preparation of multifunctional flame-retardant wood composites by crosslinking chitosan-based polymers with phytic acid functionalized UiO-66-NH2

Yaohong Yang,Yuefeng Huang,Xinjie Yang,Li Liu,Peng Wang,Zhenqiang Kan,Wei Bi,Kaimeng Xu,Guanben Du,Lianpeng Zhang

Bio-based composites can mitigate the pollution issues linked to petroleum-based materials due to their eco-friendly properties. On the other hand, bio-based functionalized metal-organic frameworks have gained attention in the field of flame retardants due to their multi-pathway flame retardant mechanism and environmentally friendly synthesis process. However, its application in wood industry is less. In this work, a novel functional adhesive and coating (ACS-MACS/PA-UiO66-NH 2 ) was developed by using phosphorus-rich biomass phytate functionalized metal-organic framework (MOF) PA-UiO66-NH 2 as a flame retardant and mixed with modified chitosan. Furthermore, using ACS-MACS/PA-UiO66-NH 2 and three-layer wooden boards, a tight cross-linked network was formed through hot pressing dehydration and condensation reactions to prepare multifunctional wood composites. The experimental results indicated that the mechanical properties of the multifunctional wood composites are excellent. Additionally, these wood composites exhibit high levels of charring and graphitization, leading to excellent flame retardancy. The preparation process of these multifunctional wood composites is straightforward, and their excellent properties provide a foundation for the development of high-performance green composite materials.

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APPLIED SURFACE SCIENCE · 2021 · IF 6.707

Design and enhancement of photocatalytic activity of porphyrin functionalized UiO-66 and Keggin unit co-doped titanium dioxide heterojunction

Tingting Sun,Xinwei Zhang,Yisheng Hu,Lei Xu,Yahui Zhao

The UiO-66-FP/HPW/TiO 2 heterojunction photocatalytic material is fabricated by one-pot solvothermal method. The crystal structure, elemental composition, morphology, and optical properties of as-prepared catalysts are well-characterized. Subsequently, the synthesized materials’ catalytic activity is evaluated by degrading rhodamine B (RhB) and ofloxacin (OFX) under visible-light illumination. It turns out that the 10 wt% UiO-66-FP/HPW/TiO 2 sample possesses the best efficiency, with 98.6% RhB and 97.2% OFX removed under identical condition, which is 4.68 and 4.14 times than that of HPW/TiO 2 , respectively. The superior efficiency can be ascribed to the construction of UiO-66-FP/HPW/TiO 2 heterostructure, better adsorption capacity of organic contaminants, enhanced visible light response, and lower recombination rate of e − -h + pairs. The quenching effect of distinct scavengers indicates that •OH is an additional significant contributor to the ternary photodegradation system besides •O 2 – and h VB + species. This constitutes another reason for the superior photocatalytic activity of UiO-66-FP/HPW/TiO 2 relative to HPW/TiO 2 . The photo-degradation efficiency of 10 wt% UiO-66-FP/HPW/TiO 2 composite is reduced by 4.68% after running five cycles. Overall, this work presents one type of efficient and reusable TiO 2 -based photocatalysts driven by visible light.

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Journal of the Taiwan Institute of Chemical Engineers · 2022 · IF 5.477

Defect-rich covalently-crosslinked UiO-66(Zr)-NH2/PVC adsorption ultrafiltration membrane for effective phosphate ions removal from water

Yong Pan,Feng Liu,Yong Zhou,Chen Zhu,Haixia Pang,Baoming Xu

Background Phosphorus in wastewater is a major environmental concern. Very small phosphorus inputs in the environment can cause algal blooms that can deplete the dissolved oxygen and decrease the water quality, leading to eutrophication. Furthermore, some algal blooms produce toxins and bacterial growth that can cause human illness through exposure to contaminated water. Therefore, It is necessary to remove phosphorus before it is discharged to the environment. Methods adsorbent enhanced adsorptive ultrafiltration (UF) has recently emerged as an advanced ion recovery technology with membrane filtration function and adsorption function, and is very effective in removing cationic bisphosphate and anionic phosphate. Significant findings Herein, a novel defect-rich and covalently-crosslinked octanoic acid (OA)-UiO-66(Zr)-NH 2 /PVC adsorption ultrafiltration membrane are designed for removal of phosphate ions in water. The OA-UiO-66-NH 2 /PVC-33 membrane achieved the adsorption capacity (∼30 mgg −1 ) and higher removal efficiency (∼90%). The OA-UiO-66(Zr)-NH 2 /PVC ultrafiltration membrane exhibited a higher water flux of 266.9 L/(m 2 ·h·bar) compared to those of pristine PVC and UiO-66-NH 2 /PVC. Filtration and cyclic stability experiments reveal that OA-UiO-66(Zr)-NH 2 /PVC membrane can maintain a high retention capacity and exhibit excellent regeneration performance after 5 cycles.

✓ 已验证 DOI 高影响因子
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Journal of Materials Chemistry A · 2024 · IF 10.7

High-efficiency photocatalytic reduction of Cr(VI) by Z-scheme electron transfer in UiO-66-NH2@HDU-25 heterojunctions

Wen Lu,Chen Wang,Wenhui Song,Zhixiong Zhang,Chengde Xie,Jianjun Wang

The heavy metal ion hexavalent chromium (Cr(VI)) in wastewater significantly threatens public health. Heterojunction photocatalysts typically demonstrate high reduction efficiency in water for Cr(VI) contamination. Overcoming the drawbacks of single metal organic frameworks (MOFs) or covalent organic frameworks (COFs), MOF@COF heterostructures inherit the advantages of large porosity, high surface area, and multiple active sites of single components. Herein, we report novel hybrid UiO-66-NH2@HDU-25 heterojunctions based on a condensation reaction. The optimal ratio of UiO-66-NH2@HDU-25 presented significantly superior photocatalytic activity to most reported MOFs and COFs due to heterojunction formation, which promoted charge separation. Under identical conditions, the optimally formulated UiO-66-NH2@HDU-25 could remove over 99% of Cr(VI), approximately 1.8 and 2.6 times the original UiO-66-NH2 and HDU-25 levels. Furthermore, the UiO-66-NH2@HDU-25 (8 : 1) heterojunction demonstrated favorable reusability and stability over five reaction cycles. Various experiments and density functional theory (DFT) calculations investigated the charge carrier transport pathways and possible photocatalytic mechanisms. The Z-scheme mechanism for the photocatalytic Cr(VI) reduction by UiO-66-NH2@HDU-25 was proposed and validated. This work aims to open new horizons for preparing novel photocatalyst heterojunctions with excellent visible light responsiveness for environmental water remediation.

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Materials Today Chemistry · 2023 · IF 7.3

Flexible core-shell PAN/CNTs@PVDF-HFP/Uio-66-NH2 hybrid nanofibers membrane for advanced lithium-ion batteries separator

Mao Guo,Siyang Dong,Jing Xiong,Xuanyang Jin,Pengfei Wan,Shengjun Lu,Yufei Zhang,Jian Xu,Haosen Fan

Flexible core-shell polyacrylonitrile (PAN)/carbon nanotubes (CNTs)@Poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)/Uio-66-NH 2 (PC@PU) hybrid nanofiber membrane was prepared by coaxial electrospinning technology. PAN polymer and CNTs particles were used as core to improve the membrane structure stability for further ensuring the thermal stability of the separator. PVDF-HFP and Uio-66-NH 2 nanoparticles were applied to reinforce the affinity of separator to electrolyte. The PC@PU composite membrane delivered high thermal stability and fantastic electrolyte affinity (545.76%). Furthermore, compared with Celgard 2325 commercial membrane, the PC@PU composite membrane exhibited higher porosity (80.22%) and higher Li + conductivity (3.43 mS/cm), leading to superior rate performance and long-term cycle stability. The cell with the PC@PU hybrid membrane displayed high specific capacity of 143 mAh/g at 1C and only 0.0259% capacity attenuation of each cycle after 1000 cycles. In addition, the PC@PU composite membrane demonstrated remarkable flexibility, and the cells with bent separators exhibited outstanding electrochemical performance. Hence, the PC@PU hybrid nanofiber membrane can pave a way for the further application in the field of secondary batteries separator.

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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2022 · IF 5.518

Poly(sodium 4-styrenesulfonate) brushes-functionalized UiO-66-NH2 metal-organic framework for high and selective adsorption of dyes

Zhuanhong Jia,Xiaojun Dai,Bin Liu,Yan Li,Chunmiao Bo

Advanced adsorbents with high adsorption capacity and adsorption selectivity are desirable. Here, a Zr-based metal-organic framework (MOF), UiO-66-NH 2 @poly(sodium 4-styrenesulfonate, Nass), was synthesized using the high surface area of MOFs as a substrate and the high grafting density of surface initiated-atom transfer radical polymerization (SI-ATRP). UiO-66-NH 2 @poly(Nass) was used to adsorb different dyes. The maximum adsorption capacity ( Q m ) of methylene blue (MB) and basic fuchsine (BF) was 299.8 and 789.2 mg·g −1 , respectively, which were higher than those of Sudan I (SD I, 6.340 mg·g −1 ), neutral red (NR, 188.1 mg·g −1 ), methyl orange (MO, 199.5 mg·g −1 ), and acid chrome blue K (AK, 122.3 mg·g −1 ). The adsorption isotherms and kinetics were investigated, and it was confirmed that the Langmuir isotherm and the pseudosecond-order kinetic model fit our adsorbents. In the binary mixed solution, the removal rate (R) of MB reached 64.44%, while that of MO was only 3.340% for MB/MO. R was 64.29% for MB and 21.97% for AK for MB/AK and 97.45% for BF and 30.03% for MO for BF/MO, verifying the preferential selectivity to adsorb basic dyes. The superior adsorption was ascribed to multiple interactions, including electrostatic interaction , hydrogen bonding , and π–π accumulation. In addition, the effect of grafting poly(Nass) on the pore size of UiO-66-NH 2 was studied. The excellent stability showed that the R dropped by less than 15.62% after five consecutive cycles. The UiO-66-NH 2 @poly(Nass) was applied in the determination of MB and BF in water, crucian carp, and green shrimp. Good linearity was observed for MB (R 2 = 0.9971) and BF (R 2 = 0.9993) in the range of 0.2–30 and 0.5–50 μg·mL -1 , respectively, with satisfactory recoveries (in the range of 87.45–101.3% for MB and 90.34–98.86% for BF), achieving favorable practicability.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2018 · IF 5.091

Selective adsorption and separation of dyes from aqueous solution by core-shell structured NH2-functionalized UiO-66 magnetic composites

Zhibo Yang,Liang Zhu,Lin Chen

Core-shell structured NH 2 -functionalized UiO-66 magnetic composites (γ-Fe 2 O 3 @C@UiO-66-NH 2 ) were fabricated via a simple, facile and green approach to investigate their adsorption behaviors towards different organic dyes (methylene blue, malachite green , acid fuchsin and acid orange II). Different characterization methods containing XRD , TEM , EDXA , FTIR, BET and XPS were used to indicate that the as-prepared γ-Fe 2 O 3 @C@UiO-66-NH 2 material exhibited core-shell structure and excellent surface performance. Adsorption experiments showed that γ-Fe 2 O 3 @C@UiO-66-NH 2 could selectively adsorb anionic dyes and effectively separate the mixture, which might be mainly ascribed to the negatively-charged anionic dyes as opposite to the positively-charged Zr metal sites in γ-Fe 2 O 3 @C@UiO-66-NH 2 . The kinetics and adsorption isotherm of acid orange II and acid fuchsin adsorption in γ-Fe 2 O 3 @C@UiO-66-NH 2 were also investigated. For acid orange II and acid fuchsin, the maximum adsorption capacity obtained from the Langmuir isotherm model was 48.12 mg/g and 31.54 mg/g, respectively. Moreover, γ-Fe 2 O 3 @C@UiO-66-NH 2 exhibited good structural stability and reusability, which suggesting that γ-Fe 2 O 3 @C@ UiO-66-NH 2 as an easy-prepared adsorbent material exhibited great application potential in the selective removal of dyes from water systems.

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ACS Applied Nano Materials · 2022 · IF 6.14

Bioinspired 3D Hierarchical UiO-66-NH2 Nanoparticle/γ-AlO(OH) Nanowire for Simultaneous Detection and Removal of Fluoride Ions

Chengyan Wang,Yangsai Lyu,Jia Li,Li Li,Tingting Li,Jie Yang,Ningning Xing,Xiaolei Zhang

Excessive fluorine can cause a serious threat to human health. It is significant but challenging to develop a straightforward and rapid way to simultaneously detect and remove excess F– from water. Herein, we presented a three-dimensional (3D) hierarchical UiO-66-NH2 nanoparticle/γ-AlO(OH) nanowire hybrid synthesized by a facile biotemplate route for simultaneous detection and removal of F– from water. We elaborately assembled two kinds of materials in a bioinspired 3D hierarchical structure as a functional unit to achieve detection and removal of dual functions. The outer UiO-66-NH2 nanoparticles served as a fluorescent sensor to detect and capture F– via a strong fluorescence enhancement effect caused by the electron transfer from F– and γ-AlO(OH) and acted as the capture unit of F–. The inner γ-AlO(OH) nanowire layer served as a F– absorbent through ion exchange between F– and γ-AlO(OH). The resulting UiO-66-NH2 nanoparticle/γ-AlO(OH) nanowire hybrid displayed excellent selectivity and sensitivity for F– detection (the detection range was 0–5 mM and the limit of detection was as low as 0.77 μM) and high capacity for F– removal (the maximum equilibrium adsorption capacity qmax was as high as 87.0 mg g–1). This dual-function material provided a strategy for simultaneously selective sensing and efficient removal of anionic pollutants from water.

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CHEMICAL ENGINEERING JOURNAL · 2020 · IF 10.652

3D-agaric like core-shell architecture UiO-66-NH2@ZIF-8 with robust stability for highly efficient REEs recovery

Mengmeng Zhang,Kun Yang,Junshuo Cui,Haibiao Yu,Yuejiao Wang,Weijun Shan,Zhenning Lou,Ying Xiong

With the ever-increasing of Rare Earth Elements (REEs) in various high technology applications, efficient recovery of REEs from liquid sources is becoming significantly important. In this work, ZIF-8 and UiO-66-NH 2 (U6N) are combined to form a 3D-agaric like core-shell structure hybrid material (U6N@ZIF-8-20), which exhibits good performance in REEs extraction. Due to the abundant adsorption sites of ZIF-8 and the excellent water stability of UiO-66-NH 2 , 3D-agaric like U6N@ZIF-8-20 showed quick adsorption rate (only 10 min to reach equilibrium), high adsorption capacity and selectivity for REEs from water compared to other reported adsorbents. Maximum adsorption capacities of U6N@ZIF-8-20 for neodymium (Nd(III)), europium (Eu(III)), gadolinium (Gd(III)) and erbium (Er(III)) achieved to 249.90, 295.28, 316.22 and 340.95 mg g -1 , respectively. U6N@ZIF-8-20 has superiority in selective adsorption of REEs from Cd(II), Zn(II), Cu(II), Mn(II) and Co(II) coexistence solution. The order of adsorption capacities for REEs is in agreement with the order of their electronegativity, ionic radius and charge density. Moreover, U6N@ZIF-8-20 showed better water stability and recyclability than single MOF. Overall, MOF@MOF hybrid material has efficiency in REEs separation from solutions, and has great advantage in the application of wastewater treating.

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ACS Applied Materials & Interfaces · 2021 · IF 9.229

UiO-66-NH-(AO) MOFs with a New Ligand BDC-NH-(CN) for Efficient Extraction of Uranium from Seawater

Lin Ma,Jian Gao,Chen Huang,Xiao Xu,Lu Xu,Renhao Ding,Hongliang Bao,Ziqiang Wang,Gang Xu,Qingnuan Li,Pengyang Deng,Hongjuan Ma

Metal–organic frameworks (MOFs) with a high surface area and excellent stability are potential candidates for uranium (U) adsorption. Amidoxime (AO) is the most widely used functional group to extract U, which is usually introduced into MOFs by two-step post-synthetic methods (PSMs). Herein, MOF UiO-66-NH-(AO) was obtained by a one-step PSM with amidoximation from UiO-66-NH-(CN), which was synthesized by a new organic ligand of 2-cyano-terephthalic acid and whose morphology was octahedron and could be well controlled with the new ligand. The one-step PSM can greatly maintain the octahedron of the MOFs. What is more, UiO-66-NH-(AO) showed good adsorption performance for U, the adsorption equilibrium was obtained within 1500 min, and the adsorption capacity of U was calculated to be 134.1 mg/g according to the Langmuir model. It also had excellent selectivity for U in the presence of high concentrations of vanadium (V), ferrum (Fe), magnesium (Mg), calcium (Ca), and zirconium (Zr). The adsorption capacity of U in natural seawater was determined to be 5.2 mg/g within 8 days. The recyclability of UiO-66-NH-(AO) in simulated seawater was demonstrated for at least four adsorption/desorption cycles. The binding mechanism was investigated by the extended X-ray absorption fine structure spectroscopy, revealing that U binding occurs in a fashion η2 motif. This study provides a reliable idea for the modification of MOFs and the potential for MOF-based materials to extract U from seawater.

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