JOURNAL OF FOOD COMPOSITION AND ANALYSIS
·
2025
·
IF 4.6
Xinran Yang,Zonglin Li,Junhui Du,Xueli Zhang,Haibin Liu,Xuechao Zhang,Lijun Li,Chuanjin Cui,Hongshuo Chen
In this paper, a SERS/electrochemical dual-channel aptamer biosensor was established for ultrasensitive detection of Pb 2+ . Firstly, the capture probe Fe 3 O 4 @Au@PAMAM@Aptamer and the signal probe AuNs@4-MBA@Au@ssDNA were chemically synthesized step by step. Secondly, the carboxyl graphene oxide (GO) was electrodeposited onto the electrode surface to gain the GO/SPCE. Meanwhile, PAMAM@Au nanomaterials were successfully synthesized and thus prepared the Aptamer/PAMAM@Au/GO/SPCE. During the process, SEM, TEM, FTIR and XPS were applied to characterize the synthesized nanomaterials which confirmed the successful synthesis of the nanomaterials. Finaly, the performance of this biosensor was evaluated in a series of Pb 2+ aqueous solutions by surface enhanced Raman (SERS) and differential pulse voltammetry (DPV). The results showed that the lowest limit of detection (LOD) was 3.16 × 10 −5 nM, and the sample recovery was 99.50–103.67 %. Furthermore, the biosensor demonstrated good specificity, repeatability, and stability. Reliable results were also obtained in actual sample testing. Therefore, it can provide a viable method for trace detection of heavy metal ions.
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高影响因子
RSC Advances
·
2015
·Vol. 5
·期 125
·102993-102999
·
IF 3.84
Luyu Yang,Wei Liu,Huanlei Wang,Shuang Liu,Jifei Wang,Jiaxin Chen
A hierarchical pore structure is believed to be an excellent architecture for metal oxide anode materials of lithium-ion batteries (LIBs). However, the difficulty and complication in synthesis limit their further application. In this work, a novel Fe3O4/C composite with a hierarchical pore carbon (HPC) network has been synthesized simply by one-step pyrolysis synthesis using ferrous gluconate as the precursor. This hierarchical porous framework derived from a loose assembly of the intersecting porous carbon rods presents a wide range of pore sizes and a rather large surface area (>226 cm2 g−1). Embedded with well-crystalline Fe3O4 particles, the resulting Fe3O4@HPC composite exhibits a high capacity of 1112 mA h g−1 at the end of the 100th cycle and an enhanced rate performance of above 600 mA h g−1 at a high current density of 2000 mA g−1. This might derive from the unique hierarchical pore system with a high overall porosity, which can not only facilitate the electrolyte diffusion but also alleviate severe volume variation efficiently in lithium ion insertion/extraction. More importantly, this provides us with a successful example to fabricate advanced anode materials simply by one-step pyrolysis of cheap organic–inorganic hybrids at low-cost.
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高影响因子
ULTRASONICS SONOCHEMISTRY
·
2023
·
IF 8.4
Deming Zhao,Yiting Liu,Chunxin Wu
The research on developing a purification technology for Cr(Ⅵ) polluted water with high efficiency and the low energy consumption is crucial for achieving several Sustainable Development Goals (SDGs). In order to achieve these goals, Fe 3 O 4 @SiO 2 -APTMS nanocomposites were prepared by Fe 3 O 4 nanoparticles modified with silica and 3-aminopropyltrimethoxysilane in the presence of ultrasonic irradiation. The nanocomposites were characterized by TEM, FT-IR, VSM, TGA, BET, XRD, XPS and these analytic results proved that the nanocomposites were successfully prepared. The influential factors of Fe 3 O 4 @SiO 2 -APTMS on Cr(Ⅵ) adsorption have been explored and better experimental conditions have been obtained. The adsorption isotherm conformed to the Freundlich model. Pseudo-second-order kinetic model provided a better correlation for the experimental data compared to other kinetic models. Thermodynamic parameters for adsorption indicated that the adsorption of Cr(Ⅵ) was a spontaneous process. It was speculated that the adsorption mechanism of this adsorbent includes redox, electrostatic adsorption and physical adsorption. In summary, the Fe 3 O 4 @SiO 2 -APTMS nanocomposites were of great significance to human health and the remediation of heavy ion pollution, contributing to achievement of the Sustainable Development Goals (SDGs), including SDG-3, SDG-6.
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MICROCHEMICAL JOURNAL
·
2022
·
IF 5.304
Honglin Qin,Yuan Tao,Ruiting Niu,Bingyan Han,Lizhen Qiao
In this work, magnetic flower-like and fluorine-doped nickel oxide composites Fe 3 O 4 @SiO 2 @F/NiO were prepared and applied for the magnetic solid-phase extraction (MSPE) of five imidazole fungicides. The obtained materials were characterized by scanning electron microscopy, X-ray diffraction, energy-dispersive X-ray photoelectron spectroscopy and Brunauer-Emmett-Teller analysis to verify the successful synthesis. The effect of some experimental parameters on the extraction efficiency were explored to optimize the MSPE conditions, including the adsorbent dosage, ultrasonic time, salt concentration, sample solution pH, elution solvent type and volume. Then, method validation was performed under the optimal conditions in combination with high-performance liquid chromatography-ultraviolet detection. The determination coefficients ranged from 0.9956 to 0.9991, and the limits of detection and limits of quantification for the imidazole fungicides were 0.1–3 μg·L −1 and 0.3–10 μg·L −1 , respectively. Moreover, the intra-day and inter-day precisions were evaluated in three different concentrations with relative standard deviations in the range of 1.34 %-13.31 % and 4.96 %-13.92 %. At last, the proposed MSPE method was used to enrich and determine imidazole fungicides in tap water, milk and green tea samples, and the spiked recoveries were in the range of 77.93 %-119.38 %, demonstrating the potential of the method in the determination of imidazole fungicides from real samples.
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Journal of Cleaner Production
·
2023
·
IF 11.1
Zhipan Wen,Shen Li,Ge Zhang,Runqiao Chen,Yalei Zhang,Xiaoping Liao,Gang Cheng,Rong Chen
Magnetic hollow Fe 3 O 4 -based Mg/Al layered double hydroxide (Fe 3 O 4 @SiO 2 @LDH) was successfully synthesized and subsequently the laboratory scale tests were conducted to systematically investigate the sequestration of roxarsone (ROX) and arsenate (As(V)). Owing to its abundant surface metal hydroxyl (M-OH) groups and exchangeable CO 3 2− groups in the interlayer of MgAl-LDH nanosheets , the obtained Fe 3 O 4 @SiO 2 @LDH exhibited remarkable behavior for As(V) and ROX removal. Both As(V) and ROX could be effectively immobilized at a relatively wide pH range (3–8), and the maximum adsorption capacities of As(V) and ROX were 96.47 and 71.67 mg/g, respectively. Meanwhile, the negligible mutual effect demonstrated the Fe 3 O 4 @SiO 2 @LDH can simultaneously remove inorganic and organic arsenic compounds . The competitive cations/anions (except for PO 4 3− ions) and ionic strength were negligible on As(V) and ROX removal, whereas the inhibitory effect stem from humic acid (HA) seemed to be more seriously for As(V) than that of ROX. Adsorption mechanism of As(V)/ROX were attributed to electrostatic attraction and ion/ligand exchange process, whereas hydrogen bonding and π-π interaction may also involve in the ROX removal. Furthermore, the excellent performance in fix-bed column tests and prominent reusability indicated this magnetic Fe 3 O 4 @SiO 2 @LDH was a promising candidate adsorbent and of great potential application in organic/inorganic As-contamination wastewater treatment .
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NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 47
·期 2
·828-837
·
IF 3.925
Tiantian Wan,Zulei Zhang,Hailong Wang,Yiwen Yang,Hanxing Yang,Jian Zhang,Yanbo Zeng,Lei Li,Jinchun Li
Chlorogenic acid (CGA), a cis-diol-containing compound, exhibits anti-inflammatory, antiviral, antimicrobial and anti-oxidation properties. Thus, selective determination of CGA in food products is extremely necessary. In this study, a boron affinity magnetic polymer named Fe3O4@SiO2@PIL was synthesized to detect the concentration of CGA in actual fruit samples. The Fe3O4@SiO2@PIL was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and thermogravimetric (TG) analysis. The results showed that the Fe3O4@SiO2@PIL has uniform morphology, good magnetic properties, suitable structure and high stability. The experimental assays showed that the Fe3O4@SiO2@PIL can detect the concentration of CGA within 7 min, and has a good linear relationship with CGA in the concentration range of 0.025–2 μM (R2 = 0.9989) with a detection limit of 10 nM (S/N = 3). Moreover, the Fe3O4@SiO2@PIL exhibited excellent selectivity and can be reused for at least 5 runs, indicating its good stability and reusability. Finally, the Fe3O4@SiO2@PIL was used to selectively separate CGA in real fruit samples with the recovery ranging from 93.4% to 103.0% and the relative standard deviation (RSD) between 0.7% and 5.1%. This study gives a new insight into the utilization of magnetic materials by grafting boric acid functionalized ionic liquids for specific and rapid detection of natural cis-diol-containing compounds.
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高影响因子
International Journal of Electrochemical Science
·
2023
·
IF 1.5
Shichao Xu,Hao Duo,Chunming Zheng,Shihuai Zhao,Shidong Song,Gabriel Simon
Diseases caused by typhoidal salmonella have led to a wide range of panic. It is thereby critically urgent to develop high-efficiency, ultrasensitive techniques for typhoidal salmonella detection. Carboxylated graphene oxide (CGO), features as one of the most crucial substrates to immobilize probe DNA for the fabrication of DNA biosensor, has been studied extensively so far. However, the reagents involved in the protocols proposed previously due to their strong alkalinity and extremely high reducing properties would impose significant impact to their performance and application. Herein, we develop a novel strategy for effective carboxylation graphene oxide with sodium citrate and chloroacetic acid. X-ray photoelectron spectroscopy (XPS) results demonstrate the density of carboxyl is improved more than twice, in consistent with the results of nuclear magnetic resonance (NMR). Furthermore, decorated with cost-effective Fe 3 O 4 NPs, the conductivity of CGO could be enhanced remarkably, furthermore, far more 5’-end amino labeled probe DNA would be stably grafted. The performance of stepwise modification of the bioelectrodes is carried out by cyclic voltammetry (CV) and electrochemical impedance spectroscopes (EIS). Differential pulse voltammetry (DPV) studies exhibit a linear response ranging from 10 -17 to 10 -9 M for target DNA analysis with the detection limit up to 3.16×10 -18 M, using methylene blue (MB) as a redox indicator under optimal conditions. In addition, the as-prepared biosensor provides predominant capability for discriminating the similar target DNA sequences. Eventually, the proposed biosensor is surveyed by real samples and it shows outstanding performance. Consequently, the developed ssDNA/Fe 3 O 4 NPs/CGO/GCE can be a promising candidate for real patient samples analysis.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2022
·
IF 6.371
Na Zhang,Shuangshuang Peng,Zhiyu Liu,Ye Li,Ju Huang,Jing Li,Hongri Wan,Shuai Zhou,Zhaojian Gao,Teng Chen
In this paper, Ag NPs-decorated magnetic Fe 3 O 4 @PDA nanocomposites have been successfully prepared. The spherical Fe 3 O 4 nanoparticles with an average size approximately 340 nm were modified by dopamine under mild conditions. Dopamine was self-polymerized surrounding Fe 3 O 4 nanoparticles and transformed into poly dopamine (PDA) layers. The PDA-encapsulated magnetic (Fe 3 O 4 @PDA) nanoparticles could in-situ reduce silver ammonium ions by the catechol groups in PDA layers. The Ag NPs with an average size ranging from 20 nm to 36 nm were densely decorated on the thin PDA shell. The resultant Fe 3 O 4 @PDA-Ag nanocomposites were employed as highly efficient catalysts for the reduction of different organic pollutants in the appearance of sodium borohydride. The Fe 3 O 4 @PDA-Ag nanocomposites also demonstrated extraordinary cycling stability when the catalyst was recycled several times for the reduction of MB. The antimicrobial tests indicated Fe 3 O 4 @PDA-Ag nanocomposites could efficiently prohibit the growth of microorganism, including various bacteria and fungi. The minimal inhibitory concentrations (MIC) for Fe 3 O 4 @PDA-Ag nanocomposites against different bacteria and fungi were also determined. The excellent catalytic activity, magnetic recyclability, and antimicrobial performance make Fe 3 O 4 @PDA-Ag a feasible candidate for the remediation of wastewater which contains multiple water soluble organic pollutants and pathogenic microorganism.
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Nanomaterials
·
2022
·Vol. 12
·期 17
·2921
·
IF 5.719
Yu Tian,Zhigang Xu,Zhimin Liu,Xiaoxi Si,Fengmei Zhang,Wei Jiang
In the present study, silica-coated magnetic nanoparticles functionalized with vancomycin (Fe3O4@SiO2@VAN) were synthesized. The Fe3O4@SiO2@VAN nanocomposite was used as a sorbent for the magnetic solid-phase extraction (MSPE) of polycyclic aromatic hydrocarbons (PAHs) from environmental water, followed by GC-MS. The nanocomposite was characterized by Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, vibrating sample magnetometry, and nitrogen sorption. Various experimental parameters were optimized, including extraction condition and desorption condition. Results show that Fe3O4@SiO2@VAN combined the advantages of nanomaterials and magnetic separation technology, showing excellent dispersibility and high selectivity for PAHs in environmental water sample. Under the optimal extraction conditions, an analytical method was established with the sensitive limit of detection (LOD) of 0.03–0.16 μg L−1. The method was successfully applied for the analysis of environmental water samples. The relative standard deviations (%) were in the range of 0.50–12.82%, and the extraction recovery (%) was in the range of 82.48% and 116.32%. MSPE-coupled gas chromatography–mass spectrometry quantification of PAHs is an accurate and repeatable method for the monitoring of PAH accumulation in environmental water samples. It also provides an effective strategy for the tracing and quantification of other environmental pollutants in complex samples.Keywords:magnetic solid-phase extraction;polycyclic aromatic hydrocarbons;vancomycin;GC-MS
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高影响因子
MOLECULES
·
2022
·Vol. 27
·期 7
·2088
·
IF 4.927
Xue-Li Liu,Yong-Hui Wang,Shu-Yue Ren,Shuang Li,Yu Wang,Dian-Peng Han,Kang Qin,Yuan Peng,Tie Han,Zhi-Xian Gao,Jian-Zhong Cui,Huan-Ying Zhou
The efficient capture of multi-pollutant residues in food is vital for food safety monitoring. In this study, in-situ-fabricated magnetic MIL-53(Al) metal organic frameworks (MOFs), with good magnetic responsiveness, were synthesized and applied for the magnetic solid-phase extraction (MSPE) of chloramphenicol, bisphenol A, estradiol, and diethylstilbestrol. Terephthalic acid (H2BDC) organic ligands were pre-coupled on the surface of amino-Fe3O4composites (H2BDC@Fe3O4). Fe3O4@MIL-53(Al) MOF was fabricated by in-situ hydrothermal polymerization of H2BDC, Al (NO3)3, and H2BDC@Fe3O4. This approach highly increased the stability of the material. The magnetic Fe3O4@MIL-53(Al) MOF-based MSPE was combined with high-performance liquid chromatography-photo diode array detection, to establish a novel sensitive method for analyzing multi-pollutant residues in milk. This method showed good linear correlations, in the range of 0.05–5.00 μg/mL, with good reproducibility. The limit of detection was 0.004–0.108 μg/mL. The presented method was verified using a milk sample, spiked with four pollutants, which enabled high-throughput detection and the accuracies of 88.17–107.58% confirmed its applicability, in real sample analysis.Keywords:magnetic metal organic framework (MMOFs);magnetic solid-phase extraction (MSPE);multi-pollutants;high-performance liquid chromatography (HPLC)
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INORGANIC CHEMISTRY COMMUNICATIONS
·
2022
·
IF 3.428
Yunfeng Lei,Xuezhong Zhang,Xiangyu Meng,Zhifei Wang
The removal of methylene blue (MB) with the magnetic separation in water treatment is of increasing attentions due to its high solubility and chemical stability, which poses a great challenge on the ecological environment and human health. Herein, with assistance of simplified modification strategies, multi-carboxyl functionalized Fe 3 O 4 @SiO 2 magnetic nanoparticles (mCMNPs) have been developed with a novel insight into the grafting densities effects on the adsorption process. The results of UV–Vis spectrometry obviously showed that the increased carboxyl content on the surface of CMNPs resulted in the significant improvement in the removal process of MB. Among different types of CMNPs, mCMNPs were chosen for the separation of MB owing to possessing the highest surface carboxyl densities 0.2363 mmol/g and exhibiting the highest removal efficiency of 96.18%. Several important factors including solution pH, initial MB concentration and sorption time were optimized to achieve the best removal efficiency. Desired adsorption capacity for MB (34.75 mg/g) was achieved using mCMNPs with the pH 10, sorption time of 100 min and initial MB concentration of 50 mg/L. The sorption isotherms and sorption kinetics can be well in agreement with the Langmuir model and pseudo-second-order kinetic model, respectively. Most importantly, the synthesized mCMNPs still exhibited high removal efficiency (63%) after 5 cycle numbers. As adsorbents, it is noted that the prepared mCMNPs possessed the excellent regeneration ability and recyclability and could be a promising adsorbent for the removal of MB in water treatment.
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高影响因子
Analytical Methods
·
2022
·Vol. 14
·期 24
·2423-2430
·
IF 3.532
Juan Du,Kai Liu,Jialei Liu,Dianbo Zhao,Yanhong Bai
Listeria monocytogenes (L. monocytogenes) is one of the most lethal pathogenic bacteria. Although the traditional microbial culture method has high sensitivity and selectivity for the diagnosis of L. monocytogenes, it is time-consuming and not suitable for on-site detection. A rapid, convenient and visualized on-site detection method is particularly needed. In this work, Fe3O4@UiO-66-NH2 was prepared for both magnetic separation and lateral flow immunoassay (LFIA) for the detection of L. monocytogenes by taking advantage of the easy separation of the magnetic core Fe3O4 and the high surface area of the outer layer UiO-66-NH2. Fe3O4@UiO-66-NH2 with a high surface area and good water-dispersibility and optical properties was synthesized by a simple hydrothermal process. It could directly adsorb on the surface of target bacteria and form Fe3O4@UiO-66-NH2-bacteria conjugates, without the labeling of an antibody. After magnetic separation and concentration, the Fe3O4@UiO-66-NH2-bacteria conjugates were detected by the antibody on the test line of the LFIA strip, resulting in a visible orange band. The capture efficiency and LFIA detection of Fe3O4@UiO-66-NH2 were optimized in this study. Under the optimal conditions, a good linear correlation between the test line intensity and the concentration of L. monocytogenes was obtained in the range of 105–108 CFU mL−1, and the limit of detection was 2.2 × 106 CFU mL−1 by the naked eye. The Fe3O4@UiO-66-NH2-based LFIA strip showed strong specificity for L. monocytogenes, and the detection took 45 min without culture enrichment. Therefore, the proposed Fe3O4@UiO-66-NH2-based strip showed the advantages of simple synthesis, being label-free, low cost, good selectivity and convenience.
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