ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2017
·Vol. 409
·期 22
·5239-5247
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IF 3.431
Xie Lijun,Liu Shuqin,Han Zhubing,Jiang Ruifen,Zhu Fang,Xu Weiqin,Su Chengyong,Ouyang Gangfeng
The fiber coating is the key part of the solid-phase microextraction (SPME) technique, and it determines the sensitivity, selectivity, and repeatability of the analytical method. In this work, amine (NH 2 )-functionalized material of Institute Lavoisier (MIL)-53(Al) nanoparticles were successfully synthesized, characterized, and applied as the SPME fiber coating for efficient sample pretreatment owing to their unique structures and excellent adsorption properties. Under optimized conditions, the NH 2 -MIL-53(Al)-coated fiber showed good precision, low limits of detection (LODs) [0.025–0.83 ng L -1 for synthetic musks (SMs) and 0.051–0.97 ng L -1 for organochlorine pesticides (OCPs)], and good linearity. Experimental results showed that the NH 2 -MIL-53(Al) SPME coating was solvent resistant and thermostable. In addition, the extraction efficiencies of the NH 2 -MIL-53(Al) coating for SMs and OCPs were higher than those of commercially available SPME fiber coatings such as polydimethylsiloxane, polydimethylsiloxane–divinylbenzene, and polyacrylate. The reasons may be that the analytes are adsorbed on NH 2 -MIL-53(Al) primarily through π – π interactions, electron donor–electron acceptor interactions, and hydrogen bonds between the analytes and organic linkers of the material. Direct immersion (DI) SPME–gas chromatography–mass spectrometry methods based on NH 2 -MIL-53(Al) were successfully applied for the analysis of tap and river water samples. The recoveries were 80.3–115% for SMs and 77.4–117% for OCPs. These results indicate that the NH 2 -MIL-53(Al) coating may be a promising alternative to SPME coatings for the enrichment of SMs and OCPs.
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高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2023
·
IF 10.9
Huan Yao,Ruifeng Zhang,Yu Wen,Yue Liu,Gang Yu,Zhi-Hui Xie
Metal-organic framework [MOF, i.e., NH 2 -MIL-53(Al)] modified TiO 2 (NMT) composite photoanodes were successfully prepared by hydrothermal synthesis and were used for the photoelectrochemical cathodic protection (PECCP) of nickel-plated magnesium alloy (Mg/Ni). Results showed that the synthesis temperature significantly impacted the morphology and PECCP performance of the NMT photoanodes. The NMT@150 photoanode prepared at a reaction temperature of 150 °C exhibited the best PECCP performance and produced a current density of 1980 μA cm −2 under visible light irradiation, which was 19.8 times higher than that of a single TiO 2 photoanode. The composite photoanode could polarize the open circuit potential of the coupled Mg/Ni electrode to -876 mV and remain relatively stable within 35 h. XPS and EPR tests showed that a Z -scheme heterojunction was formed between the NH 2 -MIL-53(Al) and TiO 2 nanotubes, allowing the photogenerated electrons to accumulate mainly on the conduction band of NH 2 -MIL-53(Al). The heterojunction greatly promoted the separation and transfer of photogenerated electron-hole in the NMT composite photoanode, significantly enhancing the PECCP performance for Mg/Ni.
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JOURNAL OF MEMBRANE SCIENCE
·
2023
·
IF 9.5
Rehan Khan,Wei-Min Liu,Ihtisham Ul Haq,Hong-Gang Zhen,Heng Mao,Zhi-Ping Zhao
Pyridine is generally found in the effluents from the synthesis of paints, rubber chemicals, vitamins, and pesticides. This study focused on improving the pervaporation (PV) performance of polyether block-amide (PEBA-2533) membranes cast on polyvinylidene fluoride (PVDF) substrate, by incorporating the MIL-53 (Al) particles to prepare mixed matrix membranes (MMMs) for pyridine separation from the aqueous solution. MIL-53 (Al) has a larger aperture size (8.5 Å) than the molecular size of the pyridine (6.0 Å), which could allow pyridine molecules to efficiently pass through its channels. The coadjacent MIL-53 particles created relatively continuous permeation pathways for the penetrants in the MMMs, which substantially enhanced the separation performance. Impressively, the resultant MMMs displayed superior pyridine separation performance at complex conditions. At 65 °C and 0.5 wt% pyridine aqueous solution, the separation factor and pyridine flux of PEBA/PVDF membrane were 17.3 and 143.5 g m −2 h −1 , which were improved using MIL-53@PEBA/PVDF MMMs to 48.1 and 226.9 g m −2 h −1 , respectively. Owing to the enhanced pyridine affinity, hydrophobic property, and thermal robustness, the resultant MMMs overcame the inherent trade-off between selectivity and permeability, and also displayed the promising long-term stability. These findings may provide valuable insights for developing novel MMMs with superior separation performance.
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CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Guiming Xie,Xingyang Bai,Yi Man,Pengju Ren,Rongrong Jin,Runduo Zhang,Kostya (Ken) Ostrikov,Zhou-jun Wang,Qingyuan Yang
Innovative catalyst design and in-depth mechanism understanding are imperative for industrialization of CO 2 hydrogenation to methanol. Herein, Al-doped Cu/ZnO catalysts, Cu/Al-ZnO-x (x = 1/32, 1/16 and 1/8, denoting Al/Zn molar ratio), were creatively synthesized using MIL-53(Al) as Al sources and reactive templates. The Cu/Al-ZnO-1/16 catalyst exhibited the highest methanol production rate among the Cu/Al-ZnO-x catalysts, which was 1.93 times as active as the conventional Cu/Al-ZnO-1/16-C catalyst using Al(NO 3 ) 3 ·9H 2 O as Al source. Structural characterizations reveal that the use of MIL-53(Al) led to higher S BET , more uniform Al distribution, more abundant oxygen vacancies, more appropriate metal-support interactions and larger amount of medium basic sites. Mechanism studies demonstrate that Al doping would markedly induce oxygen vacancy formation on Cu-ZnO interfaces and thus significantly boost methanol synthesis activity. This work offers a facile approach to develop efficient methanol synthesis catalysts and provides new insights into the nature of Al promotion in Cu/ZnO-based catalysts.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2018
·
IF 11.698
He Xiao,Wenyao Zhang,Qiushi Yao,Liulian Huang,Lihui Chen,Bruno Boury,Zhongwei Chen
Metal organic frameworks (MOFs) are exploited in many applications of materials science and very recently were investigated as precursors or reagents for material synthesis. In a new way different from previous approaches, here we introduce for the first time the synthesis of metal oxide M x O y in the presence of M-free MOF acting partially as a sacrificial template and as a provider of doping metal atom. We demonstrate this approach in the case of ZnO prepared by a simple hydrothermal method in the presence of a Zn-free MOF like MIL-53(Al) or MIL-125(Ti). The resulting ZnO show low content of Al or Ti < 2% and properties are significantly different depending on whether MIL-53(Al) or MIL-125(Ti) are used or if no MOF is present. The nature and presence of MOF has different major effects on the morphology, the specific surface area of as prepared ZnO and also on the oxygen defects in its crystal structure. Corroborating the XPS, UV–vis DRS, PL, EPR and DFT studies evidence the role of such O-defects on band gap narrowing for samples calcined at 400 °C. These exhibit high efficiency in photodegradation of methyl orange (MO) compared to ZnO prepared in MOF-free conditions or previous literatures. The kinetics of MO degradation is different depending on the morphology, the specific surface and oxygen defects. The present data open the door to a new approach of the synthesis of metal oxides and a control of their properties.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2025
·
IF 8.5
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.
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高影响因子
ANALYTICAL SCIENCES
·
2023
·Vol. 39
·期 6
·925-933
·
IF 1.6
Tang Tingfan,Li Xiaohui,Zhu Jiaqing,Huang Wenyi,Cheng Hao,Feng Jun
In this paper, a polymer monolithic column based on poly (Butyl methacrylate-co-ethylene glycol dimethacrylate) (poly (BMA-co-EDGMA)) doped with MIL-53(Al) metal–organic framework (MOF) was prepared using an in situ polymerization method. The characteristics of MIL-53(Al)-polymer monolithic column were studied through scanning electron microscopy (SEM), Fourier transform infrared spectrometry (FT-IR), energy-dispersive spectroscopy (EDS), X-ray powder diffractometry (XRD), and nitrogen adsorption experiment. Due to its large surface area, the prepared MIL-53(Al)-polymer monolithic column has good permeability and high extraction efficiency. Using MIL-53(Al)-polymer monolithic column for solid-phase microextraction (SPME), coupled to pressurized capillary electrochromatography (pCEC), a method for the determination of trace chlorogenic acid and ferulic acid in sugarcane was established. Under optimized conditions, chlorogenic acid and ferulic acid have a good linear relationship ( r ≥ 0.9965) within the concentration range of 50.0–500 µg/mL, the detection limit is 0.017 µg/mL, and the relative standard deviation (RSD) is less than 3.2%. The spike recoveries of chlorogenic acid and ferulic acid were 96.5% and 96.7%, respectively. The results indicate that the method is sensitive, practical, and convenient. It has been successfully applied to the separation and detection of trace organic phenolic compounds in sugarcane samples. Graphical abstract
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MOLECULES
·
2020
·Vol. 25
·期 4
·897
·
IF 3.267
Qian-Chun Zhang,Guang-Ping Xia,Jun-Yi Liang,Xiao-Lan Zhang,Li Jiang,Yu-Guo Zheng,Xing-Yi Wang
In this study, a novel monolithic capillary column based on a NH2-MIL-53(Al) metal–organic framework (MOF) incorporated in poly (3-acrylamidophenylboronic acid/methacrylic acid-co-ethylene glycol dimethacrylate) (poly (AAPBA/MAA-co-EGDMA)) was prepared using an in situ polymerization method. The characteristics of the MOF-polymer monolithic column were investigated by scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, X-ray diffractometry, Brunauer-Emmett-Teller analysis, and thermogravimetric analysis. The prepared MOF-polymer monolithic column showed good permeability, high extraction efficiency, chemical stability, and good reproducibility. The MOF-polymer monolithic column was used for in-tube solid-phase microextraction (SPME) to efficiently adsorb trace sulfonamides from food samples. A novel method combining MOF-polymer-monolithic-column-based SPME with ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) was successfully developed. The linear range was from 0.015 to 25.0 µg/L, with low limits of detection of 1.3–4.7 ng/L and relative standard deviations (RSDs) of < 6.1%. Eight trace sulfonamides in fish and chicken samples were determined, with recoveries of the eight analytes ranging from 85.7% to 113% and acceptable RSDs of < 7.3%. These results demonstrate that the novel MOF-polymer-monolithic-column-based SPME coupled with UHPLC-MS/MS is a highly sensitive, practical, and convenient method for monitoring trace sulfonamides in food samples previously extracted with an adequate solvent.Keywords:monolithic capillary column;metal-organic framework;sulfonamides;solid-phase microextraction;ultra-high performance liquid chromatography-tandem mass spectrometry
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FOOD CHEMISTRY
·
2025
·
IF 9.8
Hongbo Li,Hao Wang,Meiyi Cao,Xing Tong,Shuo Wang,Mingfei Pan
The fluoroquinolone-enrofloxacin (ENR) residue in animal-derived foods poses a significant threat to human health, thereby necessitating developing precise, efficient, and user-friendly detection methods. This study developed a dual-mode fluorescence-colorimetric immunosensing platform using the composite of bimetallic nanoparticles integrated with metal-organic frameworks (Au/Pt NPs@NH 2 -MIL-53(Al)). The Au/Pt NPs with biocompatibility and peroxidase-like activity were modified onto fluorescent NH 2 -MIL-53(Al) and conjugated with Ab 2 to construct signal probes. The platform enables dual-mode quantitative analysis through the competitive binding of ENR and ENR-BSA conjugate to signal probes. It demonstrated a wider linear range (0.08–180 ng/mL) and high sensitivity [LOD: 0.068 ng/mL (fluorescence), 0.066 ng/mL (colorimetric), and 0.074 ng/mL (smartphone-assisted color recognition)]. In real sample analyses, the recoveries ranged from 86.7 % to 106.7 %, with satisfactory stability (RSD ≤ 4.4 %, n = 3). The dual-signal mode facilitates results self-calibration, enhancing reliability, while smartphone-assisted color recognition enables on-site, convenient screening, offering great potential for ENR detection in complex food matrices.
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ANALYST
·
2012
·Vol. 137
·期 22
·5411-5419
·
IF 4.23
Xiang-Feng Chen,Hao Zang,Xia Wang,Jian-Guang Cheng,Ru-Song Zhao,Chuan-Ge Cheng,Xiao-Qing Lu
In this paper, the potential applications of metal–organic framework (MOF) materials as fiber coatings for the solid-phase microextraction (SPME) of polycyclic aromatic hydrocarbons (PAHs) in water samples were explored. Fibers coated with MIL-53(Al, Cr, Fe) materials were fabricated by an adhesive method for SPME. The quantitation was performed by gas chromatography–tandem mass spectrometry (GC–MS/MS) using the multiple reaction monitoring mode. Among the three MIL-53(M) coatings, MIL-53(Al) showed the highest extraction efficiency towards PAHs under the current fabrication procedure. Under optimized conditions, the MIL-53(Al)-coated fiber showed good precision (relative standard deviation <12.5%), low detection limits (0.10 ng L−1 to 0.73 ng L−1, S/N = 3), and good linearity (R2 > 0.98) for aqueous solutions containing 16 PAH . The fiber also offered high thermal and chemical stability. The method developed based on MIL-53(Al) SPME–GC–MS/MS was successfully applied in the analysis of real water samples. Based on the simulation results, the PAHs were adsorbed on MIL-53(Al) primarily through the hydrophobic and π–π interactions between PAHs and the organic linker of the material. The results presented in this paper indicate that water-stable MOF materials have great potential for the SPME of aromatic compounds in water samples.
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JOURNAL OF CHROMATOGRAPHIC SCIENCE
·
2024
·
IF 1.5
Yang Shu-Tong,Cao Yi-Wen,Zeng Zi-Ying,Gang Zheng,Chen Min,Du Bing-Yan,Su Miao-Miao,Yang Zhong-Hua,Tang Zhu-Hua,Zeng Yun-Liu
In this work, a magnetic adsorption material based on metal–organic framework (Fe3O4@ZnAl-LDH@MIL-53(Al)) was synthesized and used as an adsorbent in the process of magnetic solid phase extraction. Then, a high-performance liquid chromatograph was used to quantitatively detect triazole fungicides in samples. In order to verify the successful preparation of the material, a series of characterization analyses were carried out. Besides, the key parameters that may affect the extraction efficiency have been optimized, and under optimal conditions the three triazole fungicides showed good linearity in the range of 10–1000 μg/L (R2 ≥ 0.9796); Limit of detections were ranged from 0.013 to 0.030 μg/mL. Finally, the established method was applied to the detection of triazole fungicides in four fresh juice samples. The results showed that the target analyte was not detected in all the test samples. By detecting the recoveries (73.3–104.3%) and coefficient variation (RSD ≤ 6.8%) of triazole fungicides in fortified samples, it proved that this established method meets the requirements of pesticide residue analysis and showed excellent application potential.
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MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Yun Wu,Yanqun Yang,Ming Wen,Jing Xie,Linchun Bao,Shuting Yang,Xiangming Luo,Xingyi Wang,Qianchun Zhang
Monoamine neurotransmitters play vital roles in cognitive and various physiological and pathophysiological processes, but their trace levels, small sample volumes, and complex biological matrices in biological samples pose significant analytical challenges. This study developed a novel method for the simultaneous quantification of six monoamine neurotransmitters—tyrosine, vanillylmandelic acid, tryptophan, 3,4-dihydroxyphenylacetic acid, 5-hydroxyindole-3-acetic acid, and homovanillic acid—in human serum and urine. The method utilizes magnetic solid-phase extraction coupled with ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). A multifunctional magnetic composite, polyethylenimine@polymer dopamine hydrochloride@NH 2 -MIL-53(Al)-SiO 2 @Fe 3 O 4 , was synthesized, exhibiting high extraction selectivity and capacity and achieving an extraction range of 9.61–25.4 nmol/mg for the target neurotransmitters. The analytical method, optimized for the aforementioned composite, exhibited robust linearity for all six monoamine neurotransmitters, with correlation coefficients ( R 2 ) exceeding 0.998. The limits of detection (S/N = 3) ranged from 1.1 to 22 ng/L, indicating high sensitivity. Recovery rates for the targeted analytes varied between 94.5 % and 112 %, and relative standard deviations remained within the range of 1.5–9.4 %. These findings confirm that the developed methodology is sensitive, accurate, selective, and reliable for the quantitative determination of trace monoamine neurotransmitters in complex biological samples.
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