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Fe3O4@SiO2
MATERIALS & DESIGN · 2018 · IF 4.525

Design of Fe3O4@SiO2@mSiO2-organosilane carbon dots nanoparticles: Synthesis and fluorescence red-shift properties with concentration dependence

Xiaolei Li,Wei Wang,Qianli Li,Han Lin,Yue Xu,Lin Zhuang

Organosilane-functionalized carbon dots (SiCDs) immobilized silica composite nanoparticles (Fe 3 O 4 @SiO 2 @mSiO 2 -SiCDs) with dually emissive properties have been prepared by a modified sol-gel method. Such Fe 3 O 4 @SiO 2 @mSiO 2 -SiCDs nanoparticles solution exhibits blue light emission with a maximum wavelength of 470 nm at lower concentrations, and red-shifts to yellow-green light emission with maximum wavelength of 565 nm at higher concentrations, which is different with traditional carbon dots composite materials displaying strong emission only in the blue-light region. The SiCDs are immobilized in the outer mesoporous silica layer by covalent bonds via proper blending ration, which enables the nanoparticles solution to possess excellent fluorescence stability. The Fe 3 O 4 @SiO 2 @mSiO 2 -SiCDs nanoparticles show good stability, high surface area (483.19 m 2 /g), high saturation magnetization (22.1 emu/g) and low remanence (0.217 emu/g). When the concentration of nanoparticles solution is increased, the distance between the nanoparticles decreases and exhibits the concentration-mediated scattering phenomena, which result in the red-shift of fluorescent peaks. The specific structure of the Fe 3 O 4 @SiO 2 @mSiO 2 -SiCDs nanoparticles and the concentration-mediated scattering phenomena play key roles in the red-shift appearing.

CAS / MDL: 3069-29-2 57-09-0
研究领域: 材料科学 · 纳米技术 · 光学
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MICROCHEMICAL JOURNAL · 2024 · IF 4.9

Fe3O4@SiO2@MPA-TAPA-COF as a novel sorbent in magnetic solid-phase extraction coupling with UPLC-MS/MS for determining 12 sulfonamides in water and milk

Yan Qiao,Menglin Wang,Erling Guo,Ke Wang,Ling Ma,Kaoqi Lian

This study aimed to design and synthesize a novel adsorbent Fe 3 O 4 @SiO 2 @MPA-TAPA-COF material for the first time and used as an adsorbent of MSPE. It had significant potential for the pretreatment of trace analytes. The MSPE was coupled with ultra performance liquid chromatography–tandem mass spectrometry (UPLC-MS/MS) for the rapid extraction and detection of 12 sulfonamides (SAs) from water and milk samples for the first time. Several experimental parameters were optimized, including adsorbent dosage and the effects of pH, ionic strength, adsorption time, and desorption conditions. Under the optimized pretreatment and instrumental conditions, good linearity of 0.1–100 μg·L −1 with a correlation coefficient 0.9994–0.9999, low limits of detection (0.004–0.044 μg·L −1 ) and limits of quantitation (0.013–0.136 μg·L −1 ) were obtained. Moreover, the recoveries of sulfonamides in water and milk samples were in the range of 60.88 %-102.94 %, and the relative standard deviations not exceeding 9.62 %. Finally, the magnetic Fe 3 O 4 @SiO 2 @MPA-TAPA-COF material possessed the magnetic separation and high adsorption affinity for extracting SAs from real samples. This study holds great significance in enhancing the monitoring of SAs drug residues in water and milk.

CAS / MDL: 78-10-4
研究领域: 分析化学 · 环境科学 · 食品科学
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Nanoscale Advances · 2023 ·Vol. 5 ·期 18 ·4852-4862 · IF 4.7

High-performance flower-like and biocompatible nickel-coated Fe3O4@SiO2 magnetic nanoparticles decorated on a graphene electrocatalyst for the oxygen evolution reaction

Li Ye,Pengcheng Zhu,Tianxing Wang,Xiaolei Li,Lin Zhuang

The electrocatalytic oxygen evolution reaction (OER) plays a crucial role in renewable clean energy conversion technologies and has developed into an important direction in the field of advanced energy, becoming the focus of basic research and industrial development. Herein, we report the synthesis and application of flower-like nickel-coated Fe3O4@SiO2 magnetic nanoparticles decorated on a graphene electrocatalyst for the OER that exhibit high efficiency and robust durability. The catalysts were optimized using a rotating ring-disk electrode to test their oxygen evolution properties in 1.0 M KOH solution. Importantly, owing to the high specific surface area and conductivity of C3N4 and graphene, the as-synthesized Fe3O4@SiO2@NiO/graphene/C3N4 exhibits a small Tafel slope of 40.46 mV dec−1, low overpotential of 288 mV at 10 mA cm−2, and robust OER durability within a prolonged test period of 100 h. The cytotoxicity of Fe3O4@SiO2, Fe3O4@SiO2@NiO, and Fe3O4@SiO2@NiO/graphene/C3N4 was evaluated in HeLa and MC3T3-E1 cells, demonstrating that they are efficient and biocompatible catalysts for the OER. Owing to its excellent electrocatalytic efficiency and eco-friendliness, Fe3O4@SiO2@NiO/graphene/C3N4 has considerable potential as a new multifunctional composite for large-scale applications in catalysis, biology, medicine, and high-efficiency hydrogen production.

研究领域: 材料科学 · 电化学 · 生物学 · 医学
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JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES · 2015 · IF 2.729

Development of novel magnetic solid phase extraction materials based on Fe3O4/SiO2/poly(acrylamide-N,N′-methylene bisacrylamide)-Pluronic L64 composite microspheres and their application to the enrichment of natamycin

Miaomiao Tian,Yongcun Zou,Shaoyan Zhou,Tianpeng Wang,Xueju Lv,Qiong Jia

Novel magnetic adsorbents based on Fe 3 O 4 /SiO 2 /poly(acrylamide- N , N' -methylene bisacrylamide) magnetic microspheres modified with non-ionic triblock copolymer surfactant were successfully prepared as a magnetic solid phase extraction adsorbent for the determination of trace natamycin in jam samples. The adsorbent was characterized by scanning electron microscopy, transmission electron microscopy, Fourier transformed infrared spectroscopy, vibrating sample magnetometer, and X-ray diffractometer analysis, confirming that Pluronic L64 was effectively functionalized on the magnetic materials. Various experimental parameters affecting the extraction capacity were investigated including adsorbent amount, extraction time, desorption time, sample pH, and ionic strength. For recovery evaluations, the jam samples were spiked at two concentration levels of 100 and 200   μg   kg −1 of natamycin and the recovery values were in the range of 78.8–93.4%. The relative standard deviations (RSD) for the recoveries were less than 3.5%. The novel magnetic solid phase extraction method provided several advantages, such as simplicity, low environmental impact, convenient extraction procedure, and short analysis time when used for natamycin analysis.

CAS / MDL: 79-06-1 7681-93-8
研究领域: 分析化学 · 食品科学
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NEW JOURNAL OF CHEMISTRY · 2016 ·Vol. 41 ·期 4 ·1582-1590 · IF 3.277

Fabrication of Fe3O4@SiO2@Ag magnetic–plasmonic nanospindles as highly efficient SERS active substrates for label-free detection of pesticides

Qinye He,Aiwu Zhao,Lei Li,Henghui Sun,Dapeng Wang,Hongyan Guo,Mei Sun,Ping Chen

Fe3O4@SiO2@Ag magnetic–plasmonic nanospindles with efficient SERS performance and magnetic responsiveness have been successfully fabricated. Uniform and monodispersed Fe3O4@SiO2 nanospindles were prepared by a robust strategy through annealing the obtained β-FeOOH@SiO2 nanospindles in hydrogen atmospheres at 350 °C; the SiO2 shell could be regarded as an interlayer to maintain the morphology and offer a solid support for the further growth of Ag nanoparticles. Ag nanoparticles were introduced via in situ reduction of AgNO3, and the coverage rate of Ag nanoparticles anchored on Fe3O4@SiO2 was adjusted through regulating the AgNO3 concentration. Fe3O4@SiO2@Ag magnetic–plasmonic nanospindles can serve as highly efficient SERS active substrates with controllable magnetic aggregation due to steady enrichment of mass molecules in close proximity to abundant hot spots. Moreover, these nanospindles are used for label-free detection of thiram, and the detection limit is as low as 1 × 10−7 M (about 0.024 ppm), which is lower than the maximal residue limit of 7 ppm in fruits prescribed by the U.S. Environmental Protection Agency. Therefore, such magnetic–plasmonic nanospindles in the magnetic aggregation state may be potentially applied in rapid trace detection of residual pesticides or other specific analytes.

CAS / MDL: 1193-02-8 137-26-8
研究领域: 材料科学 · 分析化学
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Journal of Applied Spectroscopy · 2018 ·Vol. 85 ·期 1 ·160-165 · IF 0.611

Rapid Detection of Tetrodotoxin Using Surface-Enhanced Raman Spectroscopy and Fe3O4/SiO2/Au Gold/Magnetic Nanoparticles

Neng Jing,Wang Xujun,Jia Kan,Sun Peilong

Fe 3 O 4 nanoparticles were first modified with tetraethoxylsilane to form Fe 3 O 4 /SiO 2 nanoparticles, followed by the addition of 3-aminopropyltriethoxysilane and 3-thiolpropyltriethoxysilane to introduce –NH 2 and –SH groups to the surface of Fe 3 O 4 /SiO 2 nanoparticles. Gold nanoparticles were further assembled on the surface of Fe 3 O 4 /SiO 2 via the electrostatic adsorption of –NH 2 and the Au–S bond to produce stable core–shell Fe 3 O 4 /SiO 2 /Au gold/magnetic nanoparticles. These Fe 3 O 4 /SiO 2 /Au gold/magnetic nanoparticles were characterized by a variety of techniques such as transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX), and afterwards conjugated with tetrodotoxin antibodies (Ab) and used as a Raman active substrate (Fe 3 O 4 /SiO 2 /Au–Ab) with Rhodamine B (RhB)-labeled tetrodotoxin antibody as a Raman reporter (Ab–RhB). Upon mixing these reagents with tetrodotoxin (TTX), a sandwich complex [Fe 3 O 4 /SiO 2 /Au–Ab···TTX···Ab–RhB] was generated due to the specific antibody–antigen interactions. The immunocomplex was subsequently separated by an externally applied magnetic source and concentrated into a pellet point, where the laser interrogation of the pellet produced a strong signal characteristic of RhB. The logarithmic intensity of the signal was found to be proportional to the concentration of TTX with a limit of detection of 0.01 μg/mL and a detection linearity range of ~ 0.01–0.5 μg/mL. The established method eliminates the complicated procedures of traditional centrifuging, column separation, and incubation and achieves a rapid detection of tetrodotoxin with improved detection sensitivity.

研究领域: 分析化学 · 纳米技术 · 毒理学
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NEW JOURNAL OF CHEMISTRY · 2018 ·Vol. 42 ·期 7 ·4981-4990 · IF 3.201

Preparation and characterization of universal Fe3O4@SiO2/CdTe nanocomposites for rapid and facile detection and separation of membrane proteins

Min Wang,Ke-yan Zheng,Shao-wu Lv,Hai-feng Zou,Hong-sen Liu,Gang-lin Yan,Ai-dong Liu,Xiao-fang Fei

Besides having many important physiological functions, cell membrane proteins have been recognized as major markers for many diseases in clinical examination. The discovery of new cell membrane proteins has attracted significant research interest. Herein, a multifunctional Fe3O4@SiO2/CdTe nanocomposite was designed for the detection and separation of cell membrane proteins, which was synthesized by a covalent coupling reaction between amino groups and carboxyl groups. It can serve as a universal tool for modifying antigens or other molecules that have amino groups. To verify the feasibility and practicability of this method, a folic acid (FA)-functionalized magnetic/fluorescent nanoprobe (Fe3O4@SiO2/CdTe-NH-FA) has been developed for recognizing and separating the FA receptor on HepG2 cells. FA was fixed to the shell of Fe3O4@SiO2/CdTe nanocomposites via 1,6-hexamethylenediamine. It obviously reduces the fluorescence quenching effect of FA on magnetic/fluorescent nanocomposites. The results demonstrate that the synthesized nanoprobe Fe3O4@SiO2/CdTe-NH-FA provides excellent optical characteristics for the reliable imaging of cancer cells and has good magnetic properties to enrich and isolate cell membrane proteins. Consequently, this biological nanoprobe can be used to find, obtain, and study unknown membrane proteins and predict the occurrence of some diseases. In addition, this nanoprobe will be a potential platform for accurate cancer diagnosis and therapy in the future.

研究领域: 纳米技术 · 生物化学 · 分子生物学 · 癌症研究
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CHINESE JOURNAL OF CHEMICAL PHYSICS · 2020 ·Vol. 33 ·期 6 ·749-756 · IF 1.067

Magnetic solid-phase extraction of phthalate esters from environmental water samples using fibrous phenyl-functionalized Fe3O4@SiO2@KCC-1

Zhou Xue-zheng,Yan Xiang-yang,Zhu Ling,Ma Ming,Dai Ya,Wang Chang-guo,Zhu Li-jun,Yu Ke-jie,Liu Shao-min

A new kind of phenyl-functionalized magnetic fibrous mesoporous silica (Fe 3 O 4 @SiO 2 @KCC-1-phenyl) was prepared by copolymerization as an efficient adsorbent for the magnetic extraction of phthalate esters from environmental water samples. The obtained Fe 3 O 4 @SiO 2 @KCC-1-phenyl showed monodisperse fibrous spherical morphology, fairly strong magnetic response (29 emu/g), and an abundant π -electron system, which allowed rapid isolation of the Fe 3 O 4 @SiO 2 @KCC-1-phenyl from solutions upon applying an appropriate magnetic field. Several variables that affect the extraction efficiency of the analytes, including the type of the elution solvent, amount of adsorbent, extraction time and reusability, were investigated and optimized. Under optimum conditions, the Fe 3 O 4 @SiO 2 @KCC-1-phenyl was used for the extraction of four phthalate esters from environmental water samples followed by high-performance liquid chromatographic analysis. Validation experiments indicated that the developed method presented good linearity (0.1–20 ng/mL), low limit of detection (7.5–29 µg/L, S / N =3). The proposed method was applied to the determination of phthalate esters in different real water samples, with relative recoveries of 93%−103.4% and relative standard deviation of 0.8%–8.3%.

研究领域: 环境科学 · 分析化学
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ULTRASONICS SONOCHEMISTRY · 2023 · IF 8.4

Adsorption of Cr(Ⅵ) polluted water by Fe3O4@SiO2-APTMS nanocomposites prepared in the presence of ultrasonic irradiation for sustainable water resources utilization

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.

CAS / MDL: 7778-50-9
研究领域: 环境科学 · 材料科学 · 可持续发展研究
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RSC Advances · 2016 ·Vol. 6 ·期 89 ·86428-86435 · IF 3.289

Preparation of neutral red functionalized Fe3O4@SiO2 and its application to the magnetic solid phase extraction of trace Hg(II) from environmental water samples

Chunlai Wu,Guifen Zhu,Jing Fan,Jianji Wang

In this work, for the first time, neutral red functionalized Fe3O4@SiO2 was prepared, characterized and subsequently used for magnetic solid phase extraction of Hg(II) from environmental water samples followed by inductively coupled plasma-mass spectrometry determination. TEM images shows uniform decoration of SiO2 on the Fe3O4 surface (with a typical particle size of 220 nm). The FT-IR analysis indicates that neutral red was combined with the SiO2 surface by chemical bonds. Trace levels of Hg(II) can be extracted efficiently and selectively due to the electrostatic and coordinate interactions of Hg(II) and neutral red. Parameters affecting the quantitative recovery of Hg(II) were investigated, and the optimized values were 6.0, 25 mg, 60 min, and 5 mL of 1.0 mol L−1 HNO3 for pH value of the solution, amount of the extractant, equilibration time and volume, concentration of eluent, respectively. Under the optimized conditions, at Hg(II) concentrations as low as 2 ng mL−1, the recovery is >85%, and the enrichment factor is as high as 100. The commonly encountered ions show no interference with the extraction process. The material can be regenerated and reused at least ten times without loss of adsorption capacity (84 mg g−1). In addition, magnetic separation greatly simplifies the extraction procedure and filtration and/or centrifugation processes were avoided. The material was successfully applied for the separation and pre-concentration of low levels of Hg(II) in environmental water samples with satisfactory results.

研究领域: 分析化学 · 环境科学
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MOLECULES · 2025 ·Vol. 30 ·期 4 ·912 · IF 4.6

Immobilization of Phospholipase D on Fe3O4@SiO2-Graphene Oxide Nanocomposites: A Strategy to Improve Catalytic Stability and Reusability in the Efficient Production of Phosphatidylserine

Huiyi Shang,Juntan Wang,Bishan Guo,Haihua Zhu,Huijuan Li

Phospholipase D (PLD) plays a pivotal role in the biosynthesis of phosphatidylserine (PS), but its practical application is constrained by limitations in stability and reusability. In this study, we successfully fabricated the Fe3O4@SiO2–graphene oxide (GO) nanocomposite by chemical binding of Fe3O4@SiO2and GO. Subsequently, PLD was immobilized onto the nanocomposite via physical adsorption, with the aim of enhancing catalytic stability, reducing mass transfer resistance, and improving reusability. Under optimal conditions, the immobilization efficiency reached 84.4%, with a PLD loading capacity of 111.4 mg/gsupport. The optimal pH for PS production by immobilized PLD shifted from 6.0 to 6.5, while the optimal temperature increased from 45 °C to 50 °C. Notably, the immobilized PLD demonstrated a shorter reaction time and a higher PS yield, achieving a 95.4% yield within 90 min, compared to the free PLD (78.1% yield within 150 min), representing a 1.04-fold improvement in production efficiency. Furthermore, the immobilized PLD exhibited outstanding storage stability and thermal stability, along with remarkable reusability. Even after being reused for 10 cycles, the PS yield still stays as high as 78.3%. These findings strongly suggest that the Fe3O4@SiO2–GO immobilized PLD has the potential for the efficient production of PS.

CAS / MDL: 67-48-1 78-10-4
研究领域: 生物化学 · 纳米材料科学 · 酶工程
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E-POLYMERS · 2022 ·Vol. 22 ·期 1 ·488-504 · IF 3.074

Facile synthesis of core–shell structured magnetic Fe3O4@SiO2@Au molecularly imprinted polymers for high effective extraction and determination of 4-methylmethcathinone in human urine samples

Fangsheng Wu,Zihua Zhang,Wei Liu,Yuan Liu,Xiujuan Chen,Pingyong Liao,Qiaoying Han,Lun Song,Hong Chen,Wenbin Liu

In this study, a novel material of core–shell structured magnetic molecularly imprinted polymers (Fe 3 O 4 @SiO 2 @Au (FSA)-MIPs) was successfully prepared for the rapid and selective determination of 4-methylmethcathinone (mephedrone, 4-MMC). The adsorption capacity of FSA-MIPs is 34.7 mg·g −1 at 308 K, which is significantly higher than magnetic non-imprinted polymers profiting from the imprinting effect. The FSA-MIPs have a short equilibrium (20 min) and could be reused more than six times. Moreover, the selectivity coefficients of FSA-MIPs for 4-MMC, 3,4-dimethylmethcathinone, butylone, 4-ethylmethcathinone, acetylfentanyl, and methylene blue are 4.01, 5.65, 7.62, 12.30, and 20.87 respectively, further indicating the markedly enhanced binding selectivity of FSA-MIPs. As an adsorbent, the FSA-MIPs were successfully applied for effective extraction of 4-MMC in three human urine samples with the recovery rates ranging from 85.5–92.6%. The results confirmed that the FSA-MIPs have good prospects in the extraction and separation of synthetic cathinones, which is suitable for further application in the criminal sciences field.

研究领域: 分析化学 · 法医学
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