MICROPOROUS AND MESOPOROUS MATERIALS
·
2023
·
IF 5.2
Yunlong Li,Miao Liu,Yixian Liu,Lilong Zhou,Jilong Han,Zhengjie Li,Jimmy Yun,Runjing Liu
Two kinds of Ce-doped UiO-66 were synthesized by using CeCl 3 ·7H 2 O and (NH 4 ) 2 Ce(NO 3 ) 6 as cerium precursors, namely Ce(III)- and Ce(IV)-UiO-66. The effect of valence states of cerium precursors on adsorption performance towards Rhodamine B (RhB) was investigated for the first time. Ce atoms are in two valence states of +3 and + 4, where Ce 3+ ions turn their surfaces negatively charged. The higher cerium content (24.8%) and ratio of Ce 3+ /Ce 4+ ions (1.4:1) of Ce(IV)-UiO-66 made its surface more negatively charged, which is contributed to form stronger electrostatic interaction with cationic dyes. The adsorption amounts of RhB were 239.5 mg/g and 431.7 mg/g for Ce(III)- and Ce(IV)-UiO-66, which are 2.38 and 5.11 times higher than pristine UiO-66, respectively. The well-fit Langmuir model and pseudo-second-order model suggest a monolayer chemisorption process. The adsorption mechanism suggests that the electrostatic interaction and the complexation interaction between Ce 3+ and RhB are dominant factors affecting RhB adsorption. Since Ce 3+ severed as adsorption sites, the higher Ce content and stronger electrostatic interaction of Ce(IV)-UiO-66 together promoted its RhB adsorption than Ce(III)-UiO-66. The obtained results help to understand how the mixed-valences of incorporated metals affect the adsorption behaviors of bimetallic MOFs deeply.
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IRANIAN POLYMER JOURNAL
·
2023
·Vol. 32
·期 8
·979-990
·
IF 3.1
Fu Mengjie,Wang Chun,Lai Xing,Xiao Changfa,Ding Ying
In terms of nanofiltration (NF) membrane development, the properties of membrane substrates and thin-film composite (TFC) structures have become an important factor to determine the separation performances of NF membrane. In this paper, the method of interfacial polymerization assisted by spacer spraying was used to construct the striped structure at nanometer scale. Nanoscale striped structure was prepared successfully on PPTA (poly( p -phenylene terephthamide)) NF surface with 1.3 g/L of UiO-66-NH 2 in the aqueous phase, and the morphology gradually changed to “point shaped” structure when 2.6 g/L of UiO-66-NH 2 in the aqueous phase. The optimized PPTA/UiO-66-NH 2 NF (PU4) membranes were used for dye/salt separation of methylene blue (MB). Compared with the nascent PPTA NF membranes, it showed a higher MB rejection rate of 98.6%, along with permeation flux of 19.79 L/m 2 \(\cdot\) h \(\cdot\) MPa. The salt separation order of the PU4 membrane was Na 2 SO 4 > MgSO 4 > MgCl 2 > NaCl. The rejection rates were 96.3%, 85.4%, 53.2%, and 18.4%, respectively. Under strong acid and alkali conditions, the separation performance was rejected 86.5%, better under alkaline conditions. More importantly, after a six-time recycle, the PU4 membrane showed no significant change in separation performance, suggesting its excellent stability. The novel strategy in this study provided an approach to develop advanced UiO-66-NH 2 membranes toward sustainable molecular separation in environmental applications. Graphical abstract
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ACS Applied Nano Materials
·
2023
·
IF 5.9
Wenqian Zhao,Xu Zhang,Chang Li,Lusheng Xu,Qin Meng,Guoliang Zhang
Adding nanomaterials such as metal–organic frameworks (MOFs) into a polyamide (PA) layer to prepare forward osmosis (FO) membranes for efficient desalination has attracted great attention. However, rational design and preparation of high-quality MOF-based PA nanocomposite forward osmosis membranes still remain a big challenge. In this study, a polyamine (PA) forward osmosis (FO) membrane was fabricated via interfacial polymerization (IP) with the assistance of a UiO-66 nanocomposite interlayer to enhance desalination and antifouling performances. Polydopamine (PDA) and polyethyleneimine (PEI) were codeposited with UiO-66 and formed a hydrophilic nanocomposite intermediate layer. The substrate with the PDA/PEI/UiO-66 interlayer had better hydrophilicity, restricting the diffusion of m-phenylenediamine (MPD) and promoting the formation of a defect-free active layer. In addition, the PDA/PEI/UiO-66 interlayer not only provided additional water channels but also enhanced the interaction of the substrate and PA layer. The water flux of the PA-PDA/PEI/UiO-66 membrane reached 40.0 L m–2 h–1 with a low reverse salt flux (3.2 g m–2 h–1). Moreover, the PA-PDA/PEI/UiO-66(0.1) membrane also possessed excellent antifouling performances with a high flux recovery of 98% and a low total fouling rate of 17%, which were 18.4% higher and 43.3% lower than those of the pristine TFC membrane, respectively. These results presented that the codeposition of the PDA/PEI/MOF interlayer greatly improved the desalination and antifouling performances of the PA FO membrane.
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Analytical Methods
·
2023
·Vol. 15
·期 16
·1953-1958
·
IF 3.1
Piaotong Liu,Rusi Hao,Wenliang Sun,Junhui Li
As an important trace element in the human body, the concentration of Cu2+ has an important impact on the environment and human health, and its quantitative determination is of great significance in the fields of environmental protection and food safety. Here, a ratiometric fluorescent probe based on Tb(III)-functionalized UiO-66-type MOFs has been synthesized via a facile post-synthetic modification method by employing mixed linkers containing terephthalic acid and 2,6-pyridinedicarboxylic acid for Cu2+ detection. The blue fluorescence intensity at 440 nm from the ligands of MOFs does not change much with increasing Cu2+ concentrations and can be used as a reference signal, while the green fluorescence of Tb3+ can be rapidly and selectively quenched, causing fluorescence intensity at 547 nm to decrease. The probe can be used as a ratiometric sensor for Cu2+ detection with a good linear response and low detection limit. The use of the probe for the determination of Cu2+ in real water samples and drinks shows good practicality. This method for Cu2+ detection is simple, specific and visualized to meet the needs of environmental monitoring and food analysis and provides a new strategy for the construction of new copper ion fluorescent sensors to analyze complex samples.
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高影响因子
Journal of Cleaner Production
·
2019
·
IF 6.395
Likang Fu,Shixing Wang,Guo Lin,Libo Zhang,Qiming Liu,Houhuang Zhou,Chenxia Kang,Shuyun Wan,Hongwei Li,Sheng Wen
A new metal organic framework UiO-66-RSA (UiO-66 with hydroxyl) was prepared by the post-modification of UiO-66-NH 2 (UiO-66 with amino) with resorcyl aldehyde and was employed for the efficient and selective separation and removal of Pb(II) in aqueous media . The maximum adsorption amount of UiO-66-RSA was 189.8 mg/g at an optimal pH of 4. The adsorption isotherm and kinetic were well described by Langmuir/Dubinin-Radushkevich and pseudo-second-order models respectively. Adsorption process was monolayer chemisorption . UiO-66-RSA was regenerated by thiourea/nitric acid and the removal rate was only decreased by 3.7% after five successive cycles. The analysis of X-ray photoelectron spectroscopy suggested the adsorption mechanism lay on the complexation reaction between hydroxyl/nitrogen-containing groups and Pb(II). The UiO-66-RSA bound Pb(II) by forming double/quadri coordinated complexes. Compared with a multitude of usual metal ions , viz., Zn(II), Co(IV), Ni(II), Mg(II), Cd(II), Cu(II) and Ca(II), the Pb(II) could be absorbed selectively by UiO-66-RSA. The results indicated that the UiO-66-RSA sorbent could be of great potential in the removal of Pb(II) from aqueous solutions.
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CHEMICAL ENGINEERING JOURNAL
·
2018
·
IF 6.735
Shipeng Wan,Man Ou,Qin Zhong,Xinming Wang
Base-on the excellent optoelectronic properties, perovskite CsPbBr 3 quantum dots (QDs) have been used on perovskite solar cells and LED devices, but little research has been focused on photochemical CO 2 reduction due to their poor moisture stability. Coincidentally, metal-organic frameworks (MOFs) materials have received tremendous attention for sustainable clean energy and environmental remediation. However, the design of excellent performed MOFs is still indispensable. Therefore, the CsPbBr 3 QDs/UiO-66(NH 2 ) nanocomposites that combine the advantages of CsPbBr 3 QDs and UiO-66(NH 2 ) have been successfully designed and fabricated for the first time. Then we employ the nanocomposites as photocatalysts to convert CO 2 to chemical fuels in nonaqueous media. The resultant nanocomposites exhibit significantly improved photocatalytic activity for CO 2 reduction. When CsPbBr 3 QDs content is 15 wt%, the amount of CO can reach 98.57 μmol·g −1 . The remarkable photocatalytic performance could be ascribed to the improved electron extraction and transfer between UiO-66(NH 2 ) and CsPbBr 3 QDs, large accessible specific surface area and enhanced visible light absorption capacity. Moreover, the nanojunction shows excellent reusability for photocatalytic CO 2 reduction. This work might supply new pathway to utilize halide perovskite QDs/MOF nanocomposite in energy conversion and environmental remediation.
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FOOD CHEMISTRY
·
2024
·
IF 8.5
Yiran Wang,Xiaolong Sun,Yufeng Zhou,Jiachen Liu,Huayue Zhu,Ru Jiang,Yingjie Miao,Yongqian Fu
Quercetin (QCT) is a flavonoid with significant health benefits, necessitating sensitive detection methods for food safety and quality control . This study presents a novel UiO-66-TCPP ratiometric fluorescent probe for the quantitative and visual detection of QCT. Under optimal conditions, the fluorescence intensity of UiO-66-TCPP decreased linearly with increasing QCT concentration, with a detection limit of 26 nM. The probe demonstrated high specificity, showing no significant interference from various substances and QCT analogues. Practical applicability was confirmed by testing artificially contaminated juice samples, achieving recovery rates between 98.0% and 104.8%. Furthermore, a paper-based sensor was developed by incorporating UiO-66-TCPP onto Whatman#1 chromatography paper . This sensor exhibited stable fluorescence and a reliable, sensitive visual response to QCT concentrations, detectable via a smartphone-based color recognizer application. The UiO-66-TCPP ratiometric fluorescent probe provides a sensitive, specific, and practical method for detecting QCT in food matrices, offering significant potential for both laboratory and on-site applications.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Qingqing Wang,Wei Zhou,Claudia Li,Sibudjing Kawi,Yinhui Li
The application of photocatalysts in environmental field has emerged as a prominent research topic. Nevertheless, the efficiency of photocatalysts is reduced as the recombination of photogenerated chargers significantly, restricting their extensive use in this domain. In the present study, photocatalysts composed of bismuth molybdate/NH 2 -UiO-66(Zr) (Bi 2 MoO 6 /NH 2 -UiO-66(Zr)) featuring Z-scheme heterojunctions were effectively synthesized using a two-step hydrothermal technique. These photocatalysts exhibit remarkable photocatalytic degradation under visible light conditions. Notably, the broad planar configuration of Bi 2 MoO 6 sheets improves the separation of the photogenerated charge carriers. NH 2 -UiO-66(Zr) layered atop Bi 2 MoO 6 sheets enhances the availability of catalytically active sites, reduces charge recombination, and promotes charge transfer through the interface. The kinetic rate constant for Bi 2 MoO 6 /NH 2 -UiO-66(Zr) is around 0.00329 L mg −1 min −1 , indicating the increase of 3.78 and 41.13 times compared with pure Bi 2 MoO 6 and NH 2 -UiO-66(Zr), respectively. The efficiency for photocatalytic degradation of tetracycline using Bi 2 MoO 6 /NH 2 -UiO-66(Zr) reaches 81.72 % under visible light. Importantly, this efficiency exhibits a reduction of 10 % after five recycling cycles, demonstrating notable stability. The photocatalytic mechanism involved in tetracycline degradation was uncovered through trapping experiments and EPR, indicating that it is predominantly facilitated by the active oxidation of ·O 2 - and ·OH. The intermediates of the photocatalytic process as well as the possible degradation pathways were discussed. The creation of Bi 2 MoO 6 sheets/NH 2 -UiO-66(Zr) heterojunction photocatalysts provides a fresh approach to the development of novel catalysts, which may lead to significant advancements in environmental remediation efforts.
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ELECTROCHIMICA ACTA
·
2016
·
IF 4.803
Juan Yang,Lite Yang,Huili Ye,Faqiong Zhao,Baizhao Zeng
In this work, highly dispersed AuPd alloy nanoparticles (NPs, 3–6 nm) decorated amino-functionalized Zr(IV)-based metal–organic framework (i.e. UiO-66-NH 2 ) was prepared via a novel adsorption/reduction method in ethanol-water solution. In this process, the UiO-66-NH 2 acted as both supporting platform and protective agent. The pores of UiO-66-NH 2 could limit the aggregation and migration of AuPd alloy NPs. The resulting AuPd/UiO-66-NH 2 catalyst possessed large specific surface area and excellent stability and dispersity in aqueous media. When it was used to construct a nitrite sensor, the composite material exhibited higher catalytic activity than the metal counterparts (i.e., Au/UiO-66-NH 2 and Pd/UiO-66-NH 2 ) due to the strong metallic synergistic effect. The electrochemical study demonstrated that the AuPd/UiO-66-NH 2 based sensor had an extended linear response concentration range of 0.05–5666 μ M for nitrite detection, with a detection limit of 0.01 μ M. It was successfully applied to determine nitrite in sausage and pickle samples.
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JOURNAL OF CHROMATOGRAPHY A
·
2014
·
IF 4.258
Zhiming Yan,Jiangnan Zheng,Jinfeng Chen,Ping Tong,Minghua Lu,Zian Lin,Lan Zhang
A silica-UIO-66 composite was fabricated by a simple hydrothermal method and then applied as liquid chromatographic stationary phase for fast and efficient separation. X-ray diffraction patterns showed the presence of UIO-66 crystals in the silica-UIO-66 composites; while scanning electron microscope (SEM) images revealed that silica-UIO-66 composites were a homogeneous mixture of silica bead and UIO-66 crystals. A variety of substituted aromatics, chlorobenzene compounds and polycyclic aromatic hydrocarbons (PAHs) were used to evaluate the retention properties of the silica-UIO-66 composite packed column. Under the optimized conditions, baseline separation of ethylbenzene (EB) and styrene was obtained with high resolution and short retention time. In addition, the silica-UIO-66 composite packed column also showed some advantages in separation of positional isomers, with which baseline separation of EB and xylene, chlorotoluene and dichlorobenzene isomers was achieved. Moreover, the retention mechanisms of these compounds were also discussed in detail. The relative standard deviations (RSDs) for the separation of EB and xylene, chlorotoluene and dichlorobenzene isomers, as well as EB and styrene were 0.42–0.9%, 1.0–1.9%, 0.75–2.0%, and 0.9–2.1% for the retention time, peak area, peak height, and half peak width, respectively. The column efficiencies for EB, p-chlorotoluene, p-dichlorobenzene and styrene were 8780, 9060, 9990 and 5130 plates/m. The successful applications suggested high potentials of silica-MOFs composite as stationary phase for fast and efficient liquid chromatography separation.
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
·
2015
·Vol. 307
·期 1
·269-276
·
IF 1.034
Luo Bai-Cheng,Yuan Li-Yong,Chai Zhi-Fang,Shi Wei-Qun,Tang Quan
Metal–organic frameworks (MOFs) UiO-66 and its amine derivative (UiO-66-NH 2 ) with high surface area and unprecedented chemical stability were synthesized and first explored for U(VI) capture from aqueous solutions. At pH 5.5, U(VI) sorption reach equilibrium in ca. 4 h and the maximum sorption capacity is more than 100 mg g −1 . Moreover, they show desirable selectivity towards U(VI) over a range of competing metal ions. Sorption results demonstrate that introduction of amino groups into MOFs does not enhance U(VI) sorption, probably result from the lower activity of aromatic amines, decrease of surface area and formation of intermolecular hydrogen bonds.
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MICROCHEMICAL JOURNAL
·
2024
·
IF 4.9
Lixia Luo,Jinglin Shui,Yingying Gu,Dandan Wang,Jiangyang Qin,Yanan Wang,Yong Mei
In order to detect the cervical cancer biomarker squamous cell carcinoma antigen (SCCA) in human serum, an electrochemical immunosensor was constructed. Zirconium 1,4-dicarboxybenzene MOF (UiO-66), with a high specific surface area, was coupled with gold nanoparticles (AuNPs), creating the UiO-66@AuNPs nanomaterial. This coupling increased the sensitivity of the electrochemical immunosensor by providing many biological binding sites for antibodies to bind to Au-S bonds. Then, mesoporous carbon (CMK-3) was added to the UiO-66@AuNPs nanomaterial to obtain a CMK-3@UiO-66@AuNPs nanocomposite. This further increased the electron transfer proficiency of the material and enhanced the electrochemical signal. Finally, the sensitive detection of squamous cell carcinoma antigen (SCCA) was made possible by unique immunological responses between antigens and antibodies. Transmission electron microscopy (TEM) analysis of CMK-3@UiO-66@AuNPs revealed embedded surfaces and voids; cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) confirmed the successful assembly of the electrochemical immunosensor. The developed electrochemical immunosensor demonstrated good linearity (R 1 2 = 0.999) from 0.01 pg/mL to 10,000 pg/mL, which is the concentration range of SCCA in human serum. The limit of detection was 0.0034 pg/mL (at an S/N ratio of 3). The immunosensor exhibited excellent precision, stability and selectivity, with a high rate of recovery (98.26–101.8 %). The experimental validation studies demonstrated that the electrochemical immunosensor was effective for the detection of SCCA in human serum, offering a novel method for the early diagnosis and dynamic surveillance of cervical cancer.
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