NEW JOURNAL OF CHEMISTRY
·
2023
·Vol. 47
·期 16
·7910-7921
·
IF 3.3
Ruiyao Huang,Qi Zhu,Weixin Wang,Yuhan Hu
With the increased use of antibiotic medications, more and more ciprofloxacin (CIP) is contaminated into the environment, which could endanger both humans and ecosystems. In this work, chitosan modified Fe pretreated biochar (CS-FBC), which was produced utilizing a straightforward and reduced synthesis process, was tested for its effectiveness in the removal of CIP from an aqueous solution. CS-FBC was analyzed using XPS, XRD, BET, SEM, FTIR, and a zetasizer. In addition, we investigated how ciprofloxacin removal was influenced by a number of variables, including initial concentration, time, pH, and temperature. The findings of the experiment showed that the adsorption impact was very rapid and could reach 80% over the first 60 minutes of the overall adsorbent. The kinetic model of CS-FBC adsorbed CIP in solution was discovered to be comparable to the pseudo-second-order kinetic model, suggesting that it may be connected to chemical adsorption. By matching the adsorption properties, a maximum peak value of 76.72 mg g−1 at 35 °C was found, and the fitting was found to match better with the Langmuir isotherm model. Investigations into the adsorption thermodynamics revealed that the process was temperature dependent and instantaneous. By raising the amount of NaCl, the adsorptive power might be reduced to an extent. However, the adsorption action was seldom affected by amounts of less than 0.01 M NaCl. Furthermore, in addition to hydrogen bonding and hydrophobic interaction, the adsorption process for CS-FBC on CIP also involves electrostatic interaction and π–π electron-donor–acceptor (EDA) interaction. The adsorption rate could still be maintained at 61.25% after 7 experiments. The removal effect of CS-FBC on CIP can prove that CS-FBC is a green, economical, and sustainable adsorbent with a low preparation cost.
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ACS Applied Nano Materials
·
2023
·
IF 5.9
Dongmei Jia,Yuejin Li,Huamin Cai,Yongzheng Duan,Jing Li,Chen Ling
Capture of heavy metal ions from aqueous solutions is a critical but challenging step in environmental treatment. In this work, NH2-MIL-101(Fe) nanoparticles were synthesized by simple solvothermal methods and applied to capture Cr(VI) anions from aqueous solutions. The results revealed that NH2-MIL-101(Fe) exhibited a high capture capacity (375.2 mg g–1) and an ultrafast capture rate (4 min reaching equilibrium). The competitive effects of coexisting ions such as Cl–, HCO3–, PO43–, Cd2+, Ca2+, and Cu2+ on Cr(VI) are very weak, suggesting that the adsorption selectivity significantly enhanced by loading amino groups on MIL-101(Fe). Density functional theory (DFT) calculation was performed to better understand the adsorption mechanism of Cr(VI), showing that the amino groups could increase the adsorption energy of Cr(VI) for enhancing the adsorption capacity. Based on powder X-ray diffraction, X-ray photoelectron spectroscopy, and DFT calculations, the Cr(VI) capture mechanism by NH2-MIL-101(Fe) nanoparticles was a combination of coordination between Fe and Cr(VI), electrostatic interaction between Cr2O72– and the protonated amino group, and reduction of Cr(VI) to Cr(III).
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Jun Liu,Hui Wang,Wen-Yao Zhu,Heng-Xue Xie,Xin Li,Wen-Juan Li,Ge Bai,Meng-Jie Chang,Xiao-Jiao Chai,Hui-Ling Du,Shi-Jie Song
We present a novel method to facilely prepare magnetically recoverable AgCl/Fe 3 O 4 @MIL-100(Fe) (ACFM) nanostructures for photocatalytic degradation of rhodamine B (RhB). The ACFM was directly prepared via a simple successive ionic layer adsorption and reaction (SILAR) deposition of MIL-100(Fe) on solvothermal synthesized Ag/Fe 3 O 4 nanoparticles , in which process Ag was completely oxidized into AgCl concurrent with the formation of MIL-100(Fe). The ACFM prepared with 15 SILAR cycles exhibits 92.9% efficiency towards photodegrading RhB within 30 min under visible light illumination, which is higher than that of the individual structure of AgCl/Fe 3 O 4 , Ag/Fe 3 O 4 @MIL-100(Fe) or Fe 3 O 4 @MIL-100(Fe). The remarkably enhanced photocatalytic performance is attributed to the abundant active sites and sufficient visible light response of MIL-100(Fe), as well as effective charge separation at the heterojunction interface between AgCl and MIL-100(Fe). Furthermore, the obtained ACFM can be quickly separated from the pollutant solution with a magnet and possesses good stability for recycling photocatalysis . In light of the study, the ACFM nanostructures are believed to be applied as promising photocatalysts for practical applications.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2023
·
IF 5.2
Xiaorui Yang,Jihui Wang,Zexing Ren,Wenbin Hu
The nickel-ferric layered double hydroxides (NiFe-LDHs) film which are commonly used as catalysts was fabricated on Q235 steel in-situ via two-step hydrothermal method . And the superhydrophobic NiFe-LDH-PFDTES film was obtained by 1 H, 1 H, 2 H, 2 H-perfluorodecyltriethoxysilane (PFDTES) modification. To a certain extent, the application of NiFe-LDHs has been broadened. The structure and composition of NiFe-LDHs film and NiFe-LDH-PFDTES film were analyzed by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive spectrometer (EDS), and Fourier transform infrared (FT-IR). The wettability of films was analyzed by water contact angle testing. And the corrosion resistance of NiFe-LDHs and NiFe-LDH-PFDTES film in 3.5 wt% NaCl solution were measured by using potentiodynamic polarization curve and electrochemical impedance spectroscopy (EIS) techniques. The results show that NiFe-LDHs and NiFe-LDH-PFDTES film were successfully prepared on the surface of Q235 steel. By adjusting the preparation conditions, the NiFe-LDH-PFDTES film with optimal corrosion resistance was prepared in the condition containing the hydrothermal solution concentration is 1 unit and hydrothermal time for 6 h. The hydrophobicity changes little with the hydrothermal parameters, and all reach the state of superhydrophobic, the contact angle is greater than 150°, the sliding angle is less than 1°. For the superhydrophobic film, NiFe-LDHs has excellent synergy with PFDTES, covering of an "air film" on the rough structure of LDHs, blocking the solution from contact with the substrate, thereby providing corrosion resistance. NiFe-LDH-PFDTES film exhibits much better corrosion protective performance than NiFe-LDHs film in 3.5 wt% NaCl solution, the impedance modulus is increased about 4–5 orders of magnitude compared with Q235 steel, and the highest protection efficiency can reach 99.99%.
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JOURNAL OF CLUSTER SCIENCE
·
2023
·Vol. 34
·期 6
·3095-3103
·
IF 2.8
Liu Xiangyi,Zheng Qianye,Jia Deqi,Wang Wenwen,Zhao Hong,Tao Xiansen,Sha Jingquan
To explore novel nanozymes as colorimetric biosensors with highly activities, the ternary MIL-101(Fe)@P 2 W 18 @SWNT nanocomposite was successfully fabricated based on the optimal matching principle, namely, Wells–Dawson-type polyoxometalates (POMs, H 6 P 2 W 18 O 62 abbreviated as P 2 W 18 ) were encapsulated in a custom MIL-101(Fe) cavity, and single-walled carbon nanotubes (SWNT) was then fixed. The peroxidase-like activities of MIL-101(Fe)@P 2 W 18 @SWNT nanocomposite were evaluated by detecting hydrogen peroxide (H 2 O 2 ) and glucose (GLC). Compared with the MIL-101(Fe), P 2 W 18 and SWNT, the MIL-101(Fe)@P 2 W 18 @SWNT exhibits better peroxidase-like properties and stability due to the nature of all components and their optimal synergy. Based on the excellent catalytic activity of MIL-101(Fe)@P 2 W 18 @SWNT , two colorimetric biosensors for detecting H 2 O 2 and GLC with linear ranges of 0–80 μM (H 2 O 2 ) and 0–150 μM (GLC) were constructed, and the low detection limit of 0.3 μM for H 2 O 2 and 0.2 μM for GLC are superior to the most reported nanozymes. The work opens a promising route in constructing heterogeneous MOFs and POMs-based nanozymes for biosensing application.
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JOURNAL OF MATERIALS SCIENCE
·
2023
·Vol. 58
·期 23
·9446-9458
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IF 4.5
Cheng Zhipeng,Yin Jingzhou,Chu Xiaozhong,Yang Tingting,Gao Yuan,Zhong Hui,Zhang Lili
Transition metals (TMs) have an excellent catalytic effect on the thermal decomposition of ammonium perchlorate (AP). However, nanosized TM catalysts tend to agglomerate due to their high surface energy and magnetism. In this work, a new Fe/Al composite catalyst was synthesized by loading Fe nanoparticles onto Al powder through a facile replacement route, and its effect on the thermal decomposition stability of AP and AP-based propellants was investigated. Morphological and structural characterization showed that Fe nanoparticles were successfully decorated on the Al surface without noticeable aggregation or shedding. The diameter of Fe nanoparticles was approximately 10 nm. The constructed Fe/Al composite catalyst presented a strawberry-like structure. Elemental mapping analysis revealed that the dispersion state of the Fe/Al composite catalyst was better than that of commercial Fe nanoparticles with AP. Thermal analysis indicated that the Fe/Al composite catalyst presented excellent catalytic stability in the high-temperature decomposition (HTD) of AP, reducing the HTD temperature by approximately 100 °C. Burning tests showed that the relative standard deviations of the burning rate with the Fe/Al composite catalyst were 2.5 and 2.2% at 5 and 10 MPa, respectively, whereas those with Fe reached 17.1 and 13.9% at 5 and 10 MPa, respectively. The Fe/Al composite catalyst inherited the good dispersion of Al, effectively resolving the problems of Fe nanocatalyst agglomeration. Therefore, the as-obtained Fe/Al composite catalyst can significantly improve the thermal decomposition stability of AP and AP-based propellants and will have wide application prospects in the field of AP-based propellants.
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ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Shaoqi Zhang,Haiyang Yu,Yi Wang,Yuxiang Yan,Jun Dai,Dajun Shu,Xinglong Wu
CO2 possesses extraordinary thermodynamic stability, and its reduction reaction involves multiple electron-transfer processes. Thus, high-density electron occupation on a catalyst surface is an effective driving force for improving the photocatalytic activity. Here, we report on the fabrication of Fe-doped Bi2O3 catalysts (denoted as FexBi2-xO3) with different Fe contents using the solvothermal method. The self-assembled catalyst has a nanoflower-like morphology, and its performance of CO2 reduction to CO is improved largely dependent on the Fe content. In the sample with a 7.0% Fe content (Fe0.07Bi1.93O3), the CO evolution rate reaches 30.06 μmol g–1 h–1, which is about 6 times higher than the 4.95 μmol g–1 h–1 of pristine Bi2O3, and shows excellent photostability after three cycles, with each cycle lasting for 7 h. Theoretical calculation and spectral characterization reveal that such a good CO2 reduction reaction performance arises from effective surface occupation of Fe, which not only enhances sunlight absorption but also significantly increases the surface electron density on the double metal active sites. This work provides a new strategy for improving the photocatalytic performance by surface metal doping in some metal oxide photocatalysts.
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PubMed
高影响因子
CHEMOSPHERE
·
2023
·
IF 8.8
Qiong Wu,Chunying Dong,Maoxiang Chen,Yu Zhang,Meiqiang Cai,Yan Chen,Micong Jin,Zongsu Wei
In this study, SiO 2 -composited biochar decorated with Fe/Mn was prepared by co-pyrolysis method. The degradation performance of the catalyst was evaluated by activating persulfate (PS) to degrade tetracycline (TC). The effects of pH, initial TC concentration, PS concentration, catalyst dosage and coexisting anions on degradation efficiency and kinetics of TC were investigated. Under optimal conditions (TC = 40 mg L −1 , pH = 6.2, PS = 3.0 mM, catalyst = 0.1 g L −1 ), the kinetic reaction rate constant could reach 0.0264 min −1 in Fe 2 Mn 1 @BC-0.3SiO 2 /PS system, which was 12 times higher than that in the BC/PS system (0.00201 min −1 ). The electrochemical, X-ray diffractometer (XRD), Fourier transform infrared spectrum (FT-IR) and X-ray photoelectron spectroscopy (XPS) analysis showed that both metal oxides and oxygen-containing functional groups provide more active sites to activate PS. The redox cycle between Fe(II)/Fe(III) and Mn(II)/Mn(III)/Mn(IV) accelerated the electron transfer and sustained the catalytic activation of PS. Radical quenching experiments and electron spin resonance (ESR) measurements confirmed that surface sulfate radical (SO 4 •− ) play a key role in TC degradation . Three possible degradation pathways of TC were proposed based on high-performance liquid chromatography coupled with high-resolution mass spectrometry (HPLC-HRMS) analysis, the toxicity of TC and its intermediates was analyzed by bioluminescence inhibition test. In addition to the enhanced catalytic performance, the presence of silica also improved the stability of the catalyst, as confirmed by cyclic experiment and metal ion leaching analysis. The Fe 2 Mn 1 @BC-0.3SiO 2 catalyst, derived from low-cost metals and bio-waste materials, offer an environmentally friendly option to design and implement heterogenous catalyst system for pollutant removal in water.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Qiwen Pan,Fei Lin,Ruiqi Liu,Yilin Li,Xinyue Zhang,Rui Luo,Lingling Cai,Yang Liu,Wuguo Deng,Liru He
Nanocatalysts provide a platform for developing anti-tumor strategies by activating intratumoral chemical catalysis to produce highly toxic reactive oxygen species (ROS). However, the biological effect of nanocatalysts on tumor cells, which is pivotal for effective nanotherapy treatment, remains poorly understood. Herein, we present a general and facile method of synthesizing Fe/Ni-layered double hydroxides (LDHs) for enhanced apoptosis- and ferroptosis-induced cancer nano-therapy, as well as a potential mechanism underlying the anti-tumor effect based on transcriptome sequencing. An analysis of the chemical structure suggests that the Fe atoms interact strongly with the Ni atoms in Fe/Ni-LDH. Compared with Fe-OH and Ni-OH, Fe/Ni-LDH exhibited significantly better ROS-catalytic activity, with a V max of 5.015 × 10 −2 μM·s −1 , and generated massive amounts of •OH and O 2 •− radicals, enabling outstanding chemo-dynamic therapy. Both in vitro and in vivo experiments indicated a robust apoptosis-induced cell death pathway, increased intracellular oxidative stress, and accumulation of lipid peroxide (LPO), promoting ferroptosis-involved cancer-cell death, which was further confirmed by transcriptome sequencing. The Fe/Ni-LDH biocatalyst not only provides a robust nanoplatform for tumor suppression but also encourages further exploration and applications of nanobiocatalysts.
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高影响因子
CERAMICS INTERNATIONAL
·
2023
·
IF 5.2
Sheng-Jiang Huang,Le-Zhong Li,Xiao-Hui Wu,Jian Tang,Rui Wang,Zhe Xiong,Xin Chang
Considering how quickly wireless communication has developed, the need for the miniaturization, integration and high frequency of electronic components is more intense. The improvement of material properties is the key to solving the difficulties in the development of electronic devices. Solid-phase reactions were used to create Ni 0.5 Zn 0.4 Co 0.1 Dy x Fe 2- x O 4 (NZCDF, 0 ≤ x ≤ 0.1) ferrite ceramics. The produced NZCDF ceramic samples are discovered to still have a spinel structure. The lattice constant a and bulk density d Bulk increase when dysprosium ion is added. The saturation magnetization decreased from 82 to 71 emu/g, and the Hc increased from 18 to 23 Oe. Dysprosium can be added to ceramic samples to modify their level of polarization, lower their ε ′, and minimize their dielectric loss. The DC resistance ρ increases to 6.3 × 10 3 Ω⋅m. In the higher frequency range, with the increase of dysprosium ion content, the magnetic quality factor Q increases significantly, its peak value expands, and its corresponding frequency shifts to a higher frequency. In the high-frequency region, the magnetic quality factor Q rises dramatically, its peak value expands, and its corresponding frequency shifts to a higher frequency. The peak Q of the Ni 0.5 Zn 0.4 Co 0.1 Dy 0.1 Fe 1.9 O 4 sample increased to 14.71, and the frequency corresponding to the peak Q increased to 35.08 MHz. In short, substituting dysprosium ions for nickel-zinc-cobalt ferrite broadens the application range of ferrite ceramics in high-frequency devices. The spectrum of applications for ferrite ceramics in high-frequency devices is expanded by substituting rare earth dysprosium ions for NiZnCo ferrite ceramics.
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2023
·Vol. 30
·期 14
·40534-40550
·
IF 5.8
Fang Lei,Wu Guojian,Yao Keyu,Zhang Dongyang,Zhou Yongchao
A novel heterogeneous catalyst named MoS 2 /MIL-53(Fe, Cu) (MMFC) was prepared by hydrothermal method and applied in a heterogeneous electro-Fenton (hetero-EF) system for lomefloxacin (LOM) degradation in this work. Under the optimal conditions of current density 3 mA/cm 2 , catalyst dosage 0.100 g/L, and initial pH 6, 93.5% LOM (2 mg/L) removal efficiency was achieved in the MMFC hetero-EF system within 60 min, indicating an obvious improvement compared with the MIL-53(Fe, Cu) hetero-EF system. The good catalytic activity was attributed to more effective active sites of the catalyst and the conversion of Fe(II)/Fe(III) and Cu(I)/Cu(II) promoted by Mo(IV) in MoS 2 , which could be inferred by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) characterizations. The reusability and stability of MMFC were explored based on five cyclic experiments, and the average degradation efficiency reached 73.9%. Furthermore, the hetero-EF system could achieve the total removal of moxifloxacin and tetracycline within 6 min and 40 min, respectively. Quenching experiments revealed that the hydroxyl radicals (·OH) were the main reactive radicals while superoxide radicals (·O 2 − ) and singlet oxygen ( 1 O 2 ) played a certain part in LOM degradation. Finally, the possible mechanism of the hetero-EF process and LOM degradation pathways were proposed, including substitution, elimination, and cleavage of ring structures. Accounting for good catalytic performance, low preparation cost, and satisfactory versatility, the MMFC exhibited good potential to work as a hetero-EF catalyst for wastewater treatment.
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高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2022
·
IF 5.518
Xin Fang,Ling Tan,Haopeng Luo,Fang Jiang,Huan Chen
Designing electrocatalysts for nitrate (NO 3 - ) reduction with excellent activity, low cost and stability is of great interest. Herein we synthesized a novel transition bimetallic phosphide (CuFeP-x, x referred to the phosphidation temperature) catalyst by phosphidation using CuFe-Prussian blue analogue (PBA) nanoparticles as the precursor. The obtained CuFeP-450 maintained the morphology of nanocube with the average size of 33.0 nm and bimetallic phosphide nanoparticles formed during the phosphidation process. The higher electrocatalytic activity of CuFeP-x in electrochemical NO 3 - reduction were attained as compared to that of calcined CuFe-450, because the CuFeP-x have a lower interface impedance and the dominated species for NO 3 - reduction changes from electron to atomic H* , which effectively enhanced the removal rate. The appropriate phosphidation temperature can form a crystal structure that facilitated reaction kinetics. As a result, CuFeP-450 showed the best electrocatalytic performance for NO 3 - reduction (99.42%), and the selectivity of N 2 can reach nearly 100% under the condition of 1000 mg L −1 chloride ions . This simple method using PBA with binary transition metals to prepare bimetallic phosphide provides a new direction for designing efficient non-noble metal electrocatalysts for NO 3 - reduction.
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