LANGMUIR
·
2025
·
IF 3.9
Changhua Li,Wei Liu,Yuquan Jing,Hao Yang,Qiuping Tang,Yongxu Cui,Chao Zhang,Wei Ren,Jing Zhang,Yi He
Metal–organic framework materials with large specific surface areas are ideal choices for storing corrosion inhibitors in organic coatings. Existing reports focus on materials such as ZIF-8 and ZIF-67, which release corrosion inhibitors by disintegrating themselves upon external stimuli. This release mechanism may lead to the formation of holes within the coating, providing channels for penetration into corrosive media. In this study, NH2-MIL 101 (Cr), which is stable under acidic/alkaline conditions, was grown on Ti3C2Tx surface via a hydrothermal method. Its porous structure was utilized to load environmentally friendly MoO42– corrosion inhibitors, and a stimulus-responsive TEOS shell was wrapped as a valve to control the release of the corrosion inhibitors. The synthesis of the Ti3C2Tx-MIL 101-MoO42–-TEOS (TMIT) composite material was verified by FT-IR spectroscopy and XPS, respectively. The TMIT-epoxy (TMITP) composite coating was prepared through a solid–liquid mixing method. The surface-active groups of NH2-MIL 101 (Cr) (−NH2) enhanced the interfacial strength with the resin and the crosslinking density, significantly increasing the tensile strength and adhesion strength of the composite coating. Due to the improved interfacial strength, the low-frequency impedance value remained at 4.14 × 108 Ω cm2 after 6 cycles of accelerated cyclic electrochemical tests (−4.0 V, 30 min), which greatly shortening the evaluation period of the coating performance. Additionally, the stimulus-responsive release mechanism of the TMIT filler endowed the coating with self-healing effects, achieving corrosion inhibition in damaged areas. Notably, the acid/alkali stability of NH2-MIL 101 (Cr) ensured that few holes would form within the coating after the release of corrosion inhibitors, preventing the penetration of corrosive media. This study utilized the pores of NH2-MIL 101 (Cr) to load corrosion inhibitors and prepare self-healing composite coatings, achieving intelligent release and enhancing the corrosion resistance of coatings, thus broadening the application strategy of MOF materials in corrosion protection coatings.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Qinchao Shao,Xiubin Zhang,Pei Liang,Qiang Chen,Xiaohua Qi,Mingqiang Zou
Fabrication of a magnetic substrate based on metal–organic frameworks (MOFs) with high sensitivity and stability for surface-enhanced Raman scattering (SERS) analysis were reported in this paper. MIL-101(Cr) nanoparticle prepared via a traditional hydrothermal reaction, which was combined with Fe 3 O 4 to synthesize the Fe 3 O 4 /MIL-101(Cr) composites. Then, the concentration of chloroauric acid and the time of reduction reaction were adjusted to acquire the optimal Au/Fe 3 O 4 /MIL-101(Cr) (AF-MIL) SERS substrate. The detection ability of the substrate can down to 10 -8 mol/L for Rhodamine 6G (R6G) as probe molecule, and the relative standard deviation (RSD) is only about 4.48 %, which indicates that it possesses wonderful SERS performance and uniformity. Finally, the as-synthesized substrate has been adopted to test the trace level sulfapyridine, with its desirable detection ability can down to 10 -6 mol/L. Such desirable SERS substrate with facile and effective operation holds great promise in the fast sensitive detection of the antibiotic residue and some other pollutants in environment.
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
·
IF 8.6
Basem E. Keshta,Haojie Yu,Li Wang,Ali H. Gemeay
MIL-101(Cr) MOF (MIL-Materials of Institute Lavoisier; Metal-organic framework) as an adsorbent has great application in water treatment because of its high stability against air, temperature, and chemicals. Herein, we develop a novel value-added, sustainable, and eco-friendly green method to prepare MIL-101(Cr) hydrothermally based on organic and inorganic waste recycling (G-MIL-101(Cr)@R) without hydrofluoric acid (HF) addition. Several characterization techniques suggest that G-MIL-101(Cr)@R was successfully synthesized. Then, it was used as an adsorbent for acid blue 92 dye (AB-92) as a model of anionic dyes. The adsorption parameters were studied, such as adsorbent dose, contact time, pH, dye concentration, temperature, salinity, and dye selectivity. The results showed that the adsorption of AB-92 is a monolayer according to the Langmuir isotherm with a q max of 2176 mg/g. Adsorption kinetics follow the pseudo second-order model (R 2 = 0.99), occurring in three steps according to the intra-particle diffusion kinetic model. The adsorption of AB-92 over G-MIL-101(Cr)@R is spontaneous and exothermic. The adsorption mechanism is mainly defined by electrostatic interactions. G-MIL-101(Cr)@R can adsorb the anionic dyes more efficiently than cationic dyes. It could also be reused for up to five cycles with an uptake efficiency of not less than 80 % without any change in its structure. Finally, G-MIL-101(Cr)@R is considered a superior adsorbent for anionic dyes. So, it will pave the way for developing MIL-101(Cr), based on organic and inorganic waste recycling, as an efficient adsorbent for removing organic dyes from wastewater.
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Basem E. Keshta,Haojie Yu,Li Wang,Md Alim Uddin,Heba G. El-Attar,Amr E. Keshta,Ali H. Gemeay,Fathy Hassan,Sherif M. Eid
Fabricating an ion-to-electron transducer (IET) from waste in the solid contact screen-printed ion-selective electrodes (SC-SP-ISEs) technique is challenging because its properties determine the potential stability and reproducibility of the designed sensors. Herein, we fabricated an IET substrate from recyclable wastes, and we applied it as an IET layer in an ISE-based sensor for fast and on-site detection of lead ions (Pb 2+ ) in an environmental sample. First, MIL-101(Cr) was prepared based on a combination of PET and Cr +6 waste recycling (R-MIL-101(Cr)). Polyaniline (PANI) was polymerized over R-MIL-101(Cr) to prepare a conductive PANI@R-MIL-101(Cr) composite. Then, it was applied as an IET substrate in the construction of pb 2+ -ISE for the detection of Pb 2+ ions in sediment samples collected from Lake Idku, Egypt. Three Pb 2+ sensors were fabricated and abbreviated as sensors I, II, and III corresponded to PANI, R-MIL-101(Cr), and PANI@R-MIL-101(Cr) as IET substrates, respectively. The performance of the sensors was studied to be applied for fast and selective detection of Pb 2+ at low concentration levels. Among the fabricated sensors, PANI@R-MIL-101(Cr) shows fast response (5 sec), low detection limit (1 × 10 −7 mol/L), and long lifetime reaches 70 days with a potential drift of 0.9 mV h −1 . The electrochemical characteristics prove the fast ion-to-electron transportation in the case of PANI@R-MIL-101(Cr) owing to its lower impedance and high capacitance. In-situ polymerization of PANI significantly enhanced the conductivity of the PANI@R-MIL-101(Cr) composite. The hydrophobic nature of PANI@R-MIL-101(Cr) ensures high stability by preventing the formation of water layers at the electrode/membrane interface. These results show the great potential of the IET-based PANI@R-MIL-101(Cr) layer for Pb2 + sensing in environmental samples with low detection limits and high stability for the future development of SC-ISEs.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF CHROMATOGRAPHIC SCIENCE
·
2024
·
IF 1.5
Song Lixin,Zhang Jian,Wang Mingyu,Huang Zhipeng,Zhang Yunxia,Zhang Xing,Liang Yutao,He Juan
A novel approach for the simultaneous separation of zearalenone (ZEN) and four types of aflatoxins (AFB1, AFB2, AFG1 and AFG2) from rice samples was presented. This approach utilized modified MIL-101(Cr)-NH2 as core, with molecularly imprinted polymers (MIPs) serving as the shell. The MIL-101(Cr)-NH2 was prepared via ring-opening reaction, while the imprinted polymers were synthesized using warfarin and 4-methylumbelliferyl acetate as co-pseudo template, ethylene glycol dimethacrylate as the cross-linker and azobisisobutyronitrile as initiator. The resulting co-pseudo-template-MIPs (CPT-MIPs) were thoroughly characterized and evaluated. Adsorption studies demonstrate that the adsorption process of CPT-MIPs follows a chemical monolayer adsorption mechanism, with imprinted factors ranging from 1.24 to 1.52 and selective factors ranging from 1.29 to 1.52. Self-made columns were prepared, and the method for separation was developed and validated. The limit of detections ranged from 0.12 to 2.09 μg/kg, and the limit of qualifications ranged from 1.2 to 6.25 μg/kg. To assess the reliability of the method, ZEN and AFs were spiked at three different levels, and the recoveries ranged from 79.53 to 94.58%, with relative standard deviations of 2.90–5.78%.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
·
IF 8.6
Guangping Lei,Yang Lu,Zihan Liu,Yayun Zhang,Guojun Xi,Huiyuan Cheng,Wenji Rao,Xuhuan Guo
The greenhouse effect associated with excessive CO 2 emission has led to a series of environmental issues, thus developing excellent adsorbents for CO 2 capture from flue gas offers a sustainable approach. To combine the merit of multiple functional components, novel FeTPP@MIL-101(Cr) was prepared by incorporation of 5,10,15,20-tetrakis(4-methylphenyl)porphyrinato iron (III) chloride (FeTPP) into MIL-101(Cr) cages via in-situ packaging strategy. The cage-confined FeTPP can both regulate the pore structures of MIL-101(Cr) and provide additional binding sites for CO 2 adsorption. Profiting from extra interactions for CO 2 component and the “sieving effect” for N 2 component induced by incorporation of FeTPP, the discrepancy of isosteric heat for CO 2 and N 2 was largely amplified. Notably, the CO 2 /N 2 selectivity (15/85, v / v ) calculated by ideal adsorbed solution theory (IAST) increased from 17.1 (MIL-101 (Cr)) to 41.8 (FeTPP@MIL-101 (Cr) with FeTPP loading of 4.98 wt%) at 273 K, 100 kPa, which is 2.44 times larger than that of pristine MIL-101 (Cr) and also exceeds most reported adsorbents.
✓ 已验证
产品关联
DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2022
·
IF 9.221
Xiaodan Ding,Waqas Ahmad,Muhammad Zareef,Yawen Rong,Yunlian Zhang,Jizhong Wu,Qin Ouyang,Quansheng Chen
In this study, an ultra-sensitive and selective biosensor for the detection of enrofloxacin (ENR) in complex matrices has been established. The study intelligently converges the spectral properties of core-shell upconverted nanoparticles (UCNPs) and the excellent adsorption satiating aptitudes of metal organic frameworks (MOFs). The principle was based on the fluorescence resonance energy transfer (FRET) between aptamer-modified UCNPs as the donors and MOFs MIL-101(Cr) as the effective receptors. The spectral overlap between UCNPs fluorescence emission and MIL-101(Cr) absorption generated the FRET process under the action of π-π stacking interactions. The presence of ENR induced conformational changes in the aptamer via preferential binding, resulting in a decline in the nucleobase exposure on the surface of MIL-101(Cr) and eventually in the fluorescence recovery. The fluorescence intensity (FL) was enhanced as the ENR concentration was increased. The detection limit was 0.034 ng⋅mL −1 and the linear calibration curve between logarithmic ENR concentration and FL was achieved in the range of 0.1–1000 ng⋅mL −1 . The applicability of the platform for ENR recognition was confirmed in real fish and shrimp samples and further validated by a standard HPLC technique with no significant difference (p > 0.05). The current UCNPs-MIL-101(Cr) aptasensor proposes a fast, sensitive and quantitative detection approach for ENR in aquatic products.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COORDINATION CHEMISTRY
·
2021
·
IF 1.751
Milad Taheri
The synthesis and properties of new hybrid core-shell nanoparticles SiO2-HPW12O40@Fe3O4/EN-MIL-101(Cr) are reported. These hybrid nanomaterials were synthesized by binding of Keggin-type heteropolyacid (HPA) on diamine-activated Fe3O4 magnetic nanoparticles. The present work proposes an electroanalytical method for selective determination of losartan antihypertensive drug (LOS). Under optimal conditions, an electrochemical sensor was performed between the molecules in 0.1 M phosphate buffer (PBS) pH 6.0. Heterogeneous nanocatalysts can be easily separated from the reaction mixture using a magnet and used multiple times. The structure of the synthesized nanocatalyst was determined by various physicochemical techniques such as TEM, SEM, XRD, EDAX, TGA, and AFM.
✓ 已验证
产品关联
DOI
高影响因子
ANALYTICA CHIMICA ACTA
·
2018
·
IF 5.123
Sandip Mondal,Jianqiao Xu,Guosheng Chen,Siming Huang,Chuyu Huang,Li Yin,Gangfeng Ouyang
Antibiotics are a group of antibacterial drugs used in the treatment and prevention of bacterial diseases in humans, veterinary animals, and farmed fish. Inappropriate and excessive use of antibiotic therapy leads to antibiotic fragment in the water bodies thus affect the aquatic organisms . In this study, an amino group modified high surface area metal-organic framework (MOF) MIL-101(Cr)-NH 2 was used to prepare solid-phase microextraction (SPME) fiber to detect four different classes (total 6 ABs) of antibiotics for the first time from living tilapia fish ( Oreochromis mossambicus) by coupling SPME with high performance liquid chromatography-tandem mass spectrometry (LC-MS/MS). The extraction efficiencies of the custom-made fiber were superior as compared with the commercial C18, polydimethylsiloxane (PDMS), PDMS/divinylbenzene (DVB) and polyacrylate fibers. The custom-made fiber also exhibited excellent reproducibility with the low intra-fiber relative standard deviations (RSDs 1.5%–8.3%) and inter-fiber RSDs (7.3%–14.5%), which made it ideal for in vivo extraction in fish muscle. The as-prepared MIL-101(Cr)-NH 2 fiber was then used to determine antibiotics in the dorsal-epaxial muscle of living fish. Comparing to the traditional solid-liquid extraction (SLE) method, the SPME method showed reduced invasiveness and higher sensitivity than the SLE method. In general, this study explored a convenient, cost-effective and highly sensitive SPME method based on amino modified MOF for in vivo antibiotic detection in fish muscle.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Food Science & Nutrition
·
2022
·Vol. 10
·期 7
·2224-2235
·
IF 3.553
Zhentao Tang,Qingrong Han,Gang Yu,Fei Liu,Yuzhu Tan,Cheng Peng
Magnetic solid-phase extraction (MSPE) strategy based on the Fe 3 O 4 @PDA/MIL-101(Cr) has been proposed to separate and purify five common mycotoxins in licorice, including aflatoxin B 1 , aflatoxin G 1 , sterigmatocystin, zearalenone, and ochratoxin A. Integrating the MSPE and solid–liquid extraction/partitioning, a modified QuEChERS was established to adapt to the complex licorice samples. The Fe 3 O 4 @PDA/MIL-101(Cr) was successfully synthesized and characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and nitrogen adsorption–desorption isotherms. Sorbents with superior advantages for exclusion of matrix interference and extraction of target analytes in a short time were obtained, according to their ability of magnetic separation, high surface area (287.75 m 2 /g), large pore volume (0.61 cm 3 /g), and nanosized structure with mesopores. Prior to analysis with ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS), several key parameters that would affect the sorbents’ extraction efficiency were extensively investigated. Under the optimized conditions, the practicality of the developed method for analysis of mycotoxins in licorice samples was confirmed by adequate linearity ( R 2 ≥ 0.9967), high sensitivity (LODs and LOQs, respectively, in the ranges 0.01–0.09 and 0.02–0.30 μg/kg), acceptable recovery (78.53%–116.28%), satisfactory reusability, and good interbatch precision of the sorbents (RSDs in the ranges 6.70%–11.20% and 6.02%–10.35%, respectively). The results indicated that the established method was feasible and reliable for the environment-friendly and rapid screening of mycotoxins in complex licorice samples.
✓ 已验证
DOI
高影响因子
Petroleum Science
·
2023
·
IF 5.6
Bo-Long Jiang,Dong-Xu Zhang,Dan-Dan Yuan,Yan-Guang Chen,Tian-Zhen Hao,Hua Song
Oxidative desulfurization from fuel oil is one of the important methods for deep desulfurization. The development of efficient oxidative desulfurization catalysts is crucial for improving the desulfurization performance. Successful encapsulation of phosphotungstic acid (HPW) and ionic liquid (BMImBr) inside the mesoporous cages of MIL-101(Cr) was accomplished through a combination of “bottle around ship” and “ship in bottle” methods. The obtained BMImPW@MIL-101(Cr) composite was characterized by XRD, FTIR, BET, SEM, XPS and ICP methods. Results indicated that the BMImPW@MIL-101(Cr) composites with PW 3− loading of 23.1–50.7 wt% were obtained, demonstrating that the “bottle around ship” method is beneficial to make full use of nanocages of MIL-101(Cr) to obtain expected high loading of active PW 3 − . The BMImPW@MIL-101(Cr) exhibits excellent reusability with no evidence of leaching of active PW 3 − and BMIm + , and well-preserved structure after successive cycles of regeneration and reuse. The significantly improved stability of BMImPW@MIL-101(Cr) as compared to HPW@MIL-101(Cr) is possibly because the leaching of the active PW 3 − − sites can be greatly suppressed by forming large size of BMImPW owing to introduction of BMIm + cation. The BMImPW@MIL-101(Cr) exhibited excellent catalytic activity for solvent free oxidative desulfurization of refractory sulfides. The enhanced oxidative desulfurization activity as compared to HPW@MIL-101(Cr) can be explained by the intimate contact of sulfides with active PW 3 − sites owing the strong attraction of BMIm + cation with the sulfides.
✓ 已验证
产品关联
DOI
高影响因子
BIOSENSORS & BIOELECTRONICS
·
2021
·
IF 10.618
Xiaolin Zhong,Min Zhang,Lu'an Guo,Yongze Xie,Renfeng Luo,Wenxue Chen,Faliang Cheng,Lishi Wang
Designing a photoelectrochemical (PEC) immunosensor that can produce dual photocurrent signals which can refer to each other is a great importance but a big challenge. In this manuscript, a novel dual photocurrent signals immunosensor was constructed for the detection of α-fetoprotein (AFP). Unlike the usual method of using two composite materials to provide cathode and anode photocurrent respectively, this work applies only one compound of MIL-101 (Cr) and CdSe quantum dots (QDs). Thereinto, we found that the photocurrent polarity of MIL-101(Cr) would switch by adjusting applied voltage . And then CdSe QDs was introduced by simple ultrasound mixing to boost the dual photocurrent signals. Furthermore, in the composite of M&C, the electron transfer path between MIL-101(Cr) and CdSe QDs may switch between “Z-type” and “Ⅱ-type” by adjusting voltage. Benefiting by the dual signals, the proposed sensor can not only perform sensitively quantitative detection of α-fetoprotein (AFP), but also can intuitively estimate the accuracy and reliability of the test result by determining whether the corresponding relationship of “cathode photocurrent-analyte concentration-anode photocurrent” is established. The linear ranges of the sensing electrodes as cathode and anode are the same, both from 0.1 to 300 ng mL −1 . The limit of detection (LOD) is 0.082 ng mL −1 (S/N = 3) when it used as an anode, and the LOD is 0.054 ng mL −1 (S/N = 3) when it served as cathode. Furthermore, this sensor showed acceptable stability, reproducibility, specificity, and feasibility of detecting AFP in human serum, which has broad development prospects in the early clinical diagnosis.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）