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JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

Regulating the dissociation of LiCl and transportation of Li ions within UiO-66-NH2 framework for humidity sensing applications with superb comprehensive performances

Ying Zhang,Jie Xiong,Chao Chen,Qizheng Li,Jingjing Liu,Zhicheng Zhang

The novel humidity sensor , fabricated from inorganic electrolyte doped porous metal-organic framework composite (denoted as LiCl@UiO-66-NH 2 ), is reported in the present work. The humidity sensing properties of LiCl@UiO-66-NH 2 composites have been investigated. The much higher comprehensive sensing properties of composites are obtained in LiCl@UiO-66-NH 2 with 12.5 wt% LiCl. It shows the excellent linearity (R 2  = 0.994) in a broad relative humidity (RH) range. The impedance modulus of LiCl@UiO-66-NH 2 (12.5 wt%) decreases nearly four orders of magnitude from 33% RH to 95% RH at 100 Hz. Besides, the LiCl@UiO-66-NH 2 (12.5 wt%) humidity sensor exhibits fast response (6s) and recovery (18s) speed and excellent long-term stability. The sensing mechanism was discussed through the investigation of complex impedance curves. These results suggest that LiCl@UiO-66-NH 2 have the potential application in humidity sensing. Our work offers a promising strategy for the fabrication of high performance humidity sensors.

CAS / MDL: 10312-55-7 10026-11-6
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JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

Integration of Fe3O4@UiO-66-NH2@MON core-shell structured adsorbents for specific preconcentration and sensitive determination of aflatoxins against complex sample matrix

Chun-Yang Li,Jing-Min Liu,Zhi-Hao Wang,Shi-Wen Lv,Ning Zhao,Shuo Wang

Aflatoxins have been a hot topic in the field related into public health and ecosystem protection, and great effort has been made in developing of adsorptive materials for effective probing the target aflatoxins. Conventional materials, like metal-organic frameworks (MOFs) showed promising application in separation science. However, the cumbersome separation process, competitive adsorption are also major challenges. Regarding this, a novel magnetic micro-composite denoted as Fe 3 O 4 @UiO-66-NH 2 @MON with core-shell structure was constructed. The core of Fe 3 O 4 microspheres was coated with MOFs crystals, and then microporous organic network (MON) was introduced onto the surface of Fe 3 O 4 @UiO-66-NH 2 through a sonogashira coupling reaction. It exhibited good magnetic separation ability, which effectively simplified the pre-treatment steps. The proposed method possessed excellent selectivity and sensitivity, with detection limits in the range of 0.15-0.87 μg L −1 combination with HPLC analysis. More importantly, the MON coating significantly improved the hydro-stability of whole adsorbents, thus enhancing the adsorption efficiency and favoring the practical application of the materials. The developed Fe 3 O 4 @UiO-66-NH 2 @MON-based solid extraction method has been well-applied for real sample analysis, with the recovery of 87.3%–101.8%. We believe the newly-constructed hybrid nano-adsorbents hold great potential in further application in various analytical methods for different target analytes.

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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2023 · IF 3.8

Anti-abrasion collagen fiber-based membrane functionalized by UiO-66-NH2 with ultra-high efficiency and stability for oil-in-water emulsions separation

Xiaoxia Ye,Rixin Huang,Zhihong Zheng,Juan Liu,Jie Chen,Yuancai Lv

Membrane separation strategies offer promising platform for the emulsion separation. However, the low mechanical strength of membrane separation layers and the trade-off between separation flux and efficiency present significant challenges. In this study, we report a CFM@UiO-66-NH 2 membrane with high separation flux, efficiency and stability, through utilizing a robust anti-abrasion collagen fiber membrane (CFM) as the multifunctional support and UiO-66-NH 2 by an in-situ growth as the separation layer. The high mechanical strength of the CFM compensated for the weakness of the separation layer, while the charge-breaking effect of UiO-66-NH 2 , along with the size sieving of its constituent separating layers and the capillary effect of the collagen fibers, contributed to the potential for efficient separation. Additionally, the CFM@UiO-66-NH 2 membrane exhibited superhydrophilic properties, making it suitable for separating oil-in-water microemulsions and nanoemulsions stabilized by anionic surfactants. The membrane demonstrated remarkable separation efficiencies of up to 99.960% and a separation flux of 370.05 L m –2 h –1 . Moreover, it exhibits stability, durability, and abrasion resistance, maintaining excellent separation performance even when exposed to strong acids and alkalis without any damage to its structure and performance. After six cycles of reuse, it achieved a separation flux of 417.97 L m –2 h –1 and a separation efficiency of 99.747%. Furthermore, after undergoing 500 cycles of strong abrasion, the separation flux remained at 124.39 L m –2 h –1 , with a separation efficiency of 99.992%. These properties make it suitable for the long-term use in harsh operating environments. We attribute these properties to the electrostatic effect resulting from the amino group on UiO-66-NH 2 and its in-situ growth on the CFM, which forms a size-screening separation layer. Our work highlights the potential of the CFM@UiO-66-NH 2 membrane as an environmentally friendly size-screening material for the efficient emulsion wastewater separation.

CAS / MDL: 10312-55-7 23519-77-9
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2023 · IF 6.1

High Bioaffinity Controllable Assembly Nanocarrier UiO-66-NH2@Quantum Dot-Based Immunochromatographic Assay for Simultaneous Detection of Five Mycotoxins in Cereals and Feed

Jiayi Chen,Zehao Yang,Jianpeng Zhang,Xing Shen,Zhenlin Xu,Xiangmei Li,Hongtao Lei

Herein, the UiO-66-NH2@quantum dot (NU66@QD) was synthesized with excellent fluorescence intensity and biocompatibility, which was used to develop a multiple immunochromatographic assay (ICA) for the detection of aflatoxin B1 (AFB1), fumonisin B1 (FB1), deoxynivalenol (DON), T-2 toxins (T-2), and zearalenone (ZEN) in cereals and feed. Five monoclonal antibodies and NU66@QD were efficiently labeled by a one-step mixed method to form a multiple detection probe. The limits of detection of the proposed NU66@QD-ICA for AFB1/FB1/DON/T-2/ZEN were 0.04/0.28/0.25/0.09/0.08 μg/kg. The recoveries ranged from 82.83–117.44%, with the coefficient of variation from 2.88–11.80%. A parallel analysis in 35 naturally contaminated cereal and feed samples was confirmed by LC-MS/MS, and the results showed a good correlation (R2 > 0.9), indicating the practical reliability of the multiple NU66@QD-ICA. Overall, the introduction of the novel nanomaterial NU66@QD provides a highly sensitive and efficient multiplex detection strategy for the development of ICA.

CAS / MDL: 10312-55-7
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Journal of Water Process Engineering · 2023 · IF 7

A direct Z-scheme MoS2/NH2-MIL-68(In)-derived In2S3 photocatalyst for efficient photocatalytic reduction of Cr(VI) under visible-light irradiation

Chumin Yan,Xiaoli Dong,Yu Wang,Nan Zheng,Hongchao Ma,Xiufang Zhang

Inorganic semiconductors prepared from MOFs as sacrificial precursors are promising photocatalytic materials. In this work, the direct Z -scheme MoS 2 /NH 2 -MIL-68(In)-derived In 2 S 3 (MoS 2 /In 2 S 3 ) heterojunction composites have been synthesized by sulfidation treatment of MoS 2 /NH 2 -MIL-68(In) (MoS 2 /NM68) composites. Morphological and crystal structural results confirmed that MoS 2 was uniformly dispersed in In 2 S 3 . According to the reduction for Cr(VI) experimental results, the photocatalytic performance of MoS 2 /In 2 S 3 heterojunction composite under visible light irradiation is significantly better than that of pristine MoS 2 and In 2 S 3 , respectively. In addition, the photocatalytic activities of the MoS 2 /In 2 S 3 (II) at different pH and high concentrations of Cr(VI) were also investigated. This paper presents a novel approach to the construction of heterojunction photocatalytic materials using MOFs as sacrificial precursors.

CAS / MDL: 207398-97-8 1317-33-5
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Portable smartphone-assisted fluorescence-colorimetric multidimensional immunosensing microarray based on NH2-UiO-66@PtNPs multifunctional composite for efficient and visual detection of amantadine

Huilin Li,Jingying Yang,Xiaochun Hu,Ran Han,Shuo Wang,Mingfei Pan

Amantadine (AMD) is an antiviral drug used to treat animal-based infectious diseases such as avian influenza. However, its illegal use in animal-derived food industries endangers human health. Therefore, an efficient, portable, and visual sensor to detect AMD in food is crucial for ensuring food safety. A multifunctional nanocomposite NH 2 -UiO-66@PtNPs was exploited to design a smartphone-assisted fluorescence-colorimetric immunosensing microarray for multidimensional detection of AMD in animal-derived foods. Platinum nanoparticles (NPs) were immobilized on a Zr-based metal–organic framework (NH 2 -UiO-66). Pt NPs exhibited peroxidase-like activity, whereas NH 2 -UiO-66 stabilized Pt NPs and improved the colorimetric signal of the sensor. Moreover, the fluorescence ligand NH 2 -BDC in NH 2 -UiO-66 was released via alkaline hydrolysis, amplifying the fluorescence signal and improving detection sensitivity. The smartphone-assisted color recognition system accurately identified the color changes of the microarray. The immunocompetitive reaction of AMD and the antibody (Ab) in the microarray NH 2 -UiO-66@PtNPs@Ab 2 allowed the quantitative and visual detection of AMD in a wide concentration range (0.1–1000 ng/mL) with high sensitivity [limit of detection = 0.0022 ng/mL (fluorescence), 0.069 ng/mL (colorimetric), and 0.68 ng/mL (smartphone)]. This detection strategy was verified in AMD-spiked food samples with satisfactory recoveries (82.0–103.0%) and stability (RSD: ≤7.1%, n = 3), showing its great potential for visual screening and portable detection of other food contaminants.

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Journal of Water Process Engineering · 2023 · IF 7

Green water-etching synthesized La-MIL-101(Fe)-NH2@SiO2 yolk-shell nanocomposites with superior pH stability for efficient and selective phosphorus recovery

Shuangli Li,Yu Zhang,Sen Qiao,Jiti Zhou

Although MIL-101(Fe) has a homogeneous distribution of active metal sites, the relatively low stability of its coordination bonds limits its potential for application, especially in harsh environments. Here, a novel lanthanum-doped MIL-101(Fe)-NH 2 @mesoporous SiO 2 yolk-shell (LMFN-YS) material, synthesized by green water-etching, has effectively improved the adsorption capacity and stability of MIL-101(Fe)-NH 2 . Compared to traditional acid-base etching methods, water etching offered a more co-friendly and cost-effective approach to producing yolk-shell structures. Due to the mesoporous protective shell of mesoporous SiO 2 and more exposed active sites, the yolk-shell materials showed a faster adsorption rate (30 min) and a larger uptake capacity (240.0 mg P/g) than those of MIL-101. The material also exhibited broad range of pH stability from 2 to 10 and displayed good cyclic regeneration ability, with a removal efficiency of 75.9 % after three cycles. Additionally, it demonstrated excellent selectivity towards various coexisting anions such as Cl − , NO 3 − , SO 4 2− , CO 3 2− and HCO 3 − at diverse ionic strengths ranging from 0.001 to 1 M. The superior performance of L 1 MFN-YS (yolk-shell materials of La: Fe = 1:1) was attributed to a combination of factors, including ligand exchange between La(Fe)-OH and phosphates, Lewis acid-base interaction and electrostatic attraction. Additionally, high phosphate removal performance was observed in the real petrochemical wastewater (initial concentrations of 5.48 mg P/g) with a residual effluent concentration of 0.05 mg P/L, which was below the A-level standard of phosphate effluent in China (0.5 mg/L). This work provides a green method for preparing yolk-shell materials with improved ability to treat phosphate wastewater.

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Journal of Cleaner Production · 2023 · IF 11.1

Mechanism for regulation of a forward osmosis membrane by the SA/UiO-66-NH2 composite interlayer and the resulting lithium ion concentration performance

Miaolu He,Yushuang Li,Leihao Feng,Jiaqi Wang,Ze Liu,Lei Wang,Jin Wang,Rui Miao,Xudong Wang

The traditional thin-film composite (TFC) forward osmosis (FO) membrane has problems such as poor water permeability and low lithium concentration selectivity because the separation layer is too thick and has many defect pores. In this study, a thin and dense separation layer was obtained by constructing a sodium alginate (SA)/UiO-66-NH 2 interlayer to control the attachment amount and diffusion rate of m-phenylenediamine (MPD), which enhanced the performance of the membrane. This paper studies the effect and mechanism of the interlayer on the structure and separation performance of the FO membrane, and explores the lithium ion concentration performance of the interlayer membrane. According to the results, based on the strong interaction between the interlayer and MPD, the equilibrium concentration of MPD available for interfacial polymerization was increased and the diffusion rate of MPD was slowed, resulting in the generation of a thin and dense separation layer. Since the interlayer restricted the escape of bubbles formed in the interfacial polymerization, the separation layer showed a leaf-like structure with increased filtration area and water storage space. Due to the reduced thickness of the separation layer and its leaf-like structures, the water flux increased significantly, and the water flux of the interlayer membrane was 47.9% greater than that of the original membrane. Drawing upon the heightened density of the separation layer and secondary separation of the interlayer, the reverse solute flux was lowered by 37.4%. The interlayer membrane exhibited efficient Li + rejection (R>93%) and the concentration ratio of Li + was close to its theoretical concentration ratio at 1.46 ± 0.03.

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SENSORS AND ACTUATORS B-CHEMICAL · 2019 · IF 6.393

One-step electrochemiluminescence immunoassay for breast cancer biomarker CA 15-3 based on Ru(bpy)62+-coated UiO-66-NH2 metal-organic framework

Xin Xiong,Yao Zhang,YinFang Wang,HaiFeng Sha,Nengqin Jia

By virtue of the metal organic framework UiO-66-NH 2, an ingenious electrochemiluminescence immunosensor was successfully constructed for subtle exploration of the breast cancer biomarker CA 15-3. In this protocol, Ru(bpy) 3 Cl 2 ·6H 2 O (Ru(bpy) 3 2+ ), as a conventional luminescent reagent, provides a stable and strong luminescent signal. The UiO-66-NH 2 serves as a carrier to provide a large specific surface area for enhancing the electrochemical luminescence signal response of Ru(bpy) 3 2+ . UiO-66-NH 2 , Ru(bpy) 3 2+ are fixed together with Nafion membrane, and CA 15-3 antibody is covalently conjugated onto the membrane through the amide reaction. Ru(bpy) 3 2+ @UiO-66-NH 2 is used as the detection system. The experimental results reveal that the ECL signal decreased obviously after the CA 15-3 antigen molecule is captured on the immunosensor, with the capture of manifesting the principle of electrochemical luminescence quenching detection. Under optimal conditions, the sensor is sensitive and selective for detecting CA 15-3 with the detection range from 5 × 10 −4 to 5 × 10 2 U mL -1 and the low LOD (1.7705 × 10 -5 U mL -1 ). Furthermore, multiple experiments elucidate that the as-prepared sensor could be used for susceptibly detect CA 15-3 in actual samples, which has underlying application prospects in biological analysis.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2019 · IF 6.361

Surface-defect-rich mesoporous NH2-MIL-125 (Ti)@Bi2MoO6 core-shell heterojunction with improved charge separation and enhanced visible-light-driven photocatalytic performance

Shiyu Zhang,Meng Du,Junyan Kuang,Zipeng Xing,Zhenzi Li,Kai Pan,Qi Zhu,Wei Zhou

Mesoporous NH 2 -MIL-125(Ti)@Bi 2 MoO 6 core-shell heterojunctions with surface defects were fabricated through a facile solvothermal method . The mesoporous core-shell structure with a large relative surface area of 87.7 m 2  g −1 and narrow pore size of 8.2 nm extends the photoresponse to the range of visible light due to the narrow band gap of ∼1.89 eV. The visible-light-driven photocatalytic degradation efficiency of highly toxic dichlorophen and trichlorophenol were 93.28 and 92.19%, respectively, and the corresponding rate constants were approximately 8 and 17 times higher than the rates achieved by pristine NH 2 -MIL-125(Ti). The photocatalytic oxygen production rate was increased to 171.3 µmol g −1 . Recycling for several cycles indicates high stability, which is favorable for practical applications. The excellent photocatalytic performance can be ascribed to the formation of the core-shell heterojunctions and to the surface defects that favor charge separation and visible light absorption; the mesoporous structure offers an adequate number of surface active sites and mass transfer. This novel mesoporous core-shell photocatalyst will have potential applications in the environment, and this strategy offers a new insight into fabrication of other high-performance core-shell structure photocatalysts.

CAS / MDL: 10312-55-7
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CHEMOSPHERE · 2024 · IF 8.1

Boron nitride quantum dots supported hollow NH2-MIL-125 drive photo-Fenton-PMS system for photocatalytic tetracycline degradation: Contribution of tannic acid etching

Jun Guo,Jun Hou,Zijun Yang,Jun Xia,Jun Wu,Guoxiang You,Lingzhan Miao

NH 2 -MIL-125(Ti) materials had great potential for photocatalytic applications but had low activity due to exciton effect and narrow absorption range of visible light. The surface oxygen-containing negative functional groups of boron nitride quantum dots (BNQDs) could overcome these defects, but due to the low load capacity, a higher specific surface area of the substrate was usually required. In this paper, a hollow Ti-MOF material was developed by etching technology. The hollow structure formed by tannic acid etching broadened the absorption range of visable light and provided more alternative surfaces for loading BNQDs. The 85.2% of high tetracycline (TC) removal efficiency for the best sample (BNQDs-5@20-Ti-MOF + PMS) was obtained, which was about 56.8 and 1.9 times of the 20-Ti-MOF and BNQDs-5@20-Ti-MOF, respectively. BNQDs-5@20-Ti-MOF + PMS system showed a great TC degradation efficiency in a wide pH range (pH = 5–9). In addition, reaction temperature and the inorganic ions did not show significant inhibition effect for TC removal. Both free radical and non-free radical pathways were involved in the TC degration by BNQDs-5@20-Ti-MOF + PMS system, among which O 2 •− and 1 O 2 played the key roles. Interestingly, multiple 1 O 2 production paths contributed to the high efficiency and stability of BNQDs-5@20-Ti-MOF + PMS system. This study revealed a reasonable combination of Ti-MOF and BNQDs, which provided a new efficient photocatalyst for environmental remediation.

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CHEMISTRY-A EUROPEAN JOURNAL · 2013 ·Vol. 19 ·期 42 ·14279-14285 · IF 5.831

Studies on Photocatalytic CO2 Reduction over NH2-Uio-66(Zr) and Its Derivatives: Towards a Better Understanding of Photocatalysis on Metal–Organic Frameworks

Dengrong Sun,Yanghe Fu,Wenjun Liu,Lin Ye,Dengke Wang,Lin Yang,Xianzhi Fu,Zhaohui Li

Graphical Higher CO 2 photoreduction activity than previously studied metal–organic framework (MOF) NH 2 -MIL-125(Ti) in the presence of triethanolamine (TEOA) as the sacrificial agent under visible light is exhibited by the amino-functionalized MOF NH 2 -Uio-66(Zr). The photoinduced electron transfer from 2-aminoterephthalate linkers to Zr oxo clusters was revealed for the first time by photoluminescence studies, and the generated Zr III was detected by ESR analysis (see figure). Metal–organic framework (MOF) NH 2 -Uio-66(Zr) exhibits photocatalytic activity for CO 2 reduction in the presence of triethanolamine as sacrificial agent under visible-light irradiation. Photoinduced electron transfer from the excited 2-aminoterephthalate (ATA) to Zr oxo clusters in NH 2 -Uio-66(Zr) was for the first time revealed by photoluminescence studies. Generation of Zr III and its involvement in photocatalytic CO 2 reduction was confirmed by ESR analysis. Moreover, NH 2 -Uio-66(Zr) with mixed ATA and 2,5-diaminoterephthalate (DTA) ligands was prepared and shown to exhibit higher performance for photocatalytic CO 2 reduction due to its enhanced light adsorption and increased adsorption of CO 2 . This study provides a better understanding of photocatalytic CO 2 reduction over MOF-based photocatalysts and also demonstrates the great potential of using MOFs as highly stable, molecularly tunable, and recyclable photocatalysts in CO 2 reduction.

CAS / MDL: 10026-11-6
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