NEW JOURNAL OF CHEMISTRY
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2022
·Vol. 46
·期 36
·17438-17455
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IF 3.925
Qingcan Xiang,Zongxue Yu,Xuyang Li,Pingquan Wang,Niandan He,Yao Pang,Qiuxiang Wang,Yucheng Liu
A g-C3N4/NH2-MIL-88B(Fe)/CD@GO membrane (M2) was prepared by a simple vacuum filtration method. By embedding a Z-scheme heterojunction composite photocatalyst into graphene oxide (GO) nanosheets, not only can the water molecule transport channel be regulated, but the membrane can also be endowed with photocatalytic activity and membrane fouling is effectively alleviated. The pure water permeation flux of M2 (253.26 L m−2 h−1 bar−1) was 13 times that of the original GO membrane (18.83 L m−2 h−1 bar−1). What's more, even after 10 cycles, M2 still maintains excellent separation efficiency and flux. After six cycles, the rejection of Congo Red (CR), Malachite Green (MG) and Rhodamine B (RhB) by M2 was over 95%. At the same time, under the conditions of an extreme pH value and high salt concentration, the rejection of dye remained at the original level after six cycles. Therefore, the novel photocatalytic membrane has excellent separation performance, stability and photocatalytic activity, and can be used as a potential membrane for wastewater purification and environmental protection.
研究领域:
环境科学
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材料科学
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DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2020
·
IF 7.489
Huijing Ma,Bing Yu,Qingping Wang,Gary Owens,Zuliang Chen
While Fe-based metal-organic frameworks (MOFs) can be used to remove antibiotics by adsorption, knowledge of how antibiotics are degraded by MOFs is still limited. In this study, one Fe-based MOF, NH 2 -MIL-88B was used to remove pefloxacin from aqueous solution via a combination of adsorption and Fenton-like oxidation. NH 2 -MIL-88B exhibited a high adsorption capacity for pefloxacin (41.37 mg·g −1 ), with >99% removal efficiency within 120 min based on Fenton-like oxidation. To better understand the mechanisms involved in integrated adsorption and Fenton-like oxidation, various advanced characterization techniques were used to monitor the changes in morphology and composition of NH 2- MIL-88B before and after removal of pefloxacin. Scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) all supported adsorption and Fenton oxidation of pefloxacin. In addition, the pefloxacin degradation products identified by LC-UV and LC-MS provided information on the potential adsorption-Fenton oxidation mechanism. These results suggested that NH 2 -MIL-88B has remarkably potential to be used in an integrated adsorption and Fenton-like process for the removal of antibiotics from aqueous solution.
研究领域:
环境科学
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化学工程
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材料科学
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2022
·
IF 9.965
Ning Liu,Fuhao Fei,Wangxi Dai,Jianqiu Lei,Fukun Bi,Botao Wang,Guixiang Quan,Xiaodong Zhang,Liang Tang
Herein, a highly efficient Z-scheme SnS 2 /MIL-88B (Fe) (SnSFe) heterojunction was successfully synthesized to use both as photocatalysts and persulfate (PS) activator for ibuprofen (IBP) degradation. Flower-liked SnS 2 was uniformly loaded on MIL-88B (Fe), and SnSFe retained the original polyhedral morphology of MIL-88B (Fe). The highest removal of IBP was achieved in the presence of SnSFe with 0.5% SnS 2 (SnSFe0.5). Characteristic results and density functional theory calculations demonstrated that the enhanced degradation of IBP was due to the difference in Fermi energy levels of SnS 2 and MIL-88B (Fe) leading to electrons transferred from SnS 2 to MIL-88B (Fe), and Sn O bond was formed in SnSFe. , OH and O 2 − were the main active species in SnSFe0.5/PS/visible light system. Z-scheme heterojunction of SnSFe was constructed to propose the degradation mechanism. This research revealed that the synergism of photocatalysis and PS activation using SnS 2 /Fe-based MOFs composites possessed great potentials in wastewater remediation.
研究领域:
环境科学
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材料科学
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DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2022
·Vol. 33
·期 17
·14228-14239
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IF 2.779
Liu Jieling,Yang Jiaji,An Shuyue,Wen Meiqi,Wang Xian,Gong Rongzhou,Nie Yan
Metal-organic framework (MOF) crystals have promising applications in a number of different fields, but the growth of MOF crystals with controllable morphology and high uniformity remains a major challenge. By taking the advantage of the synergistic effects of water molecules in the mixed solvent and polyvinylpyrrolidone (PVP) surfactants, this work demonstrates an approach for the preparation of NH 2 -MIL-88B(Fe) MOF crystals with both highly customizable size and aspect ratios and high uniformity. The effects of the concentration of water in the mixed solvent and the amount of PVP surfactants on the morphology and size of the MOF crystals were investigated. The morphology and crystalline properties were characterized by scanning electron microscopy and X-ray diffraction techniques. The data showed that through controlling the concentration of water in the solvent and the amount of the PVP surfactant, the size of the MOF crystals can be tuned rather widely, over 344–5.14 μm, while the aspect ratio of the crystals can be varied widely over 1.0–7.1. Possible mechanisms for such high tunability were discussed. As an example of potential applications, the complex permeability and permittivity of MOF-derived composites (25 wt%) were measured over a wide frequency range of 2–18 GHz. The parameters were then used to evaluate the potential for electromagnetic wave absorption. The results indicate that the composite with a thickness of only 1.2 mm exhibits a “− 10 dB” absorption bandwidth of 4.1 GHz and a minimum reflection of − 20 dB. Such bandwidth and reflection properties provide inspiration for future design of lightweight, broadband electromagnetic wave absorbers from the perspective of fine morphology control.
研究领域:
材料科学
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化学工程
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电磁学
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2020
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IF 10.652
Yuexin Wang,Zhen Zhong,Yaseen Muhammad,Hui He,Zhongxing Zhao,Shuangxi Nie,Zhenxia Zhao
Engineering of monodentate ligands induced defects was proposed to modify NH 2 -MIL-88B(Fe) in order to promote its synergetic photo-Fenton catalytic degradation performance for acetamiprid (ACTM) as model neonicotinoid insecticides. Three monodentate ligands with different coordination groups (benzoic acid, pyrrole and pyrrole-2-carboxylic acid) were applied to in-situ induce ligand vacancies on NH 2 -MIL-88B(Fe). Effect of defect coordination mode on its photo-Fenton catalytic performance was investigated through the ACTM degradation reaction. Ligand defects on NH 2 -MIL-88B(Fe) would generate three merits: (1) it can modulate surface properties to enhance adsorption affinity towards ACTM; (2) it can introduce large amount of monodentate ligands and ligand vacancies in MOFs to promote light absorption and electron-hole separation capacity for photo-catalysis; (3) it can increase the amount of Fe Lewis acid sites to improve redox capacity of Fe 2+ /Fe 3+ for Fenton-catalysis. In this work, Pyrrole-2-carboxylic acid (Pac) was proved to introduce more monodentate ligands in MOFs and generate more ligand vacancies as well. As a result, ACTM can be easily captured by defective NH 2 -MIL-88B(Fe) and degraded by in-situ triggered oxidative reaction through the synergistic “photo-Fenton catalysis”. Performance measurements showed that Pac-MIL88(Fe) achieved 7.3 times higher adsorption rate and 5.5 times higher catalytic rate for ACTM than that of pristine MIL88(Fe). Moreover, total organic carbon (TOC) conversion reached 97.0% within only 90 min using Pac-MIL88(Fe) as photo-Fenton catalyst, showing 1.7 times higher than pristine MIL88(Fe). Thus, the in-situ fabrication of ligand defect-containing MIL88(Fe) can be foreseen of potential for designing new MOFs for wider practical applications.
研究领域:
环境科学
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材料科学
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化学工程
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Yutong Wang,Longhui Wang,Xinyan Yu,Xianbao Shen,Lijie Xu,Ying Zhang,Jiangtao Shi,Lu Gan
In this study, magnetic biochar bead ((AB + MIL-88)-C) was prepared by pyrolyzing MIL-88B(Fe) loaded alginate beads. The Fenton-like activity of (AB + MIL-88)-C was then investigated through activating peroxymonosulfate (PMS) for bisphenol A (BPA) degradation in water. The results demonstrated that (AB + MIL-88)-C exhibited superior BPA degradation capability (k = 0.160 min −1 ) than pristine MIL-88B(Fe) and alginate bead derived catalysts (k = 0.089 & 0.008 min −1 ), in which non-radical mechanisms including singlet oxygen ( 1 O 2 ) and electron transfer process contributed over 98 % of BPA degradation. Moreover, PMS consumption rate by (AB + MIL-88)-C during whole BPA degradation process was very low. Consequently, the non-radical pathway dominated oxidation system with low PMS consumption rate could maintain its activity regardless of the fluctuation of environmental parameters and water matrices. Besides, it was further demonstrated that the reaction system exhibited high degradation selectivity in which those pollutants with electron donating groups were more inclined to be degraded. Meanwhile, the degradation rate (ln k ) of respective pollutant in the reaction system correlated well (R 2 = 0.97) with their highest occupied molecular orbital position. This study provides a strategy for the development of non-radical oxidation systems with high pollutant degradation efficiency, stability and selectivity.
研究领域:
环境科学
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材料科学
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化学工程
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产品关联
DOI
高影响因子
OPTICAL MATERIALS
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2021
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IF 3.08
Xuyang Li,Zongxue Yu,Liangyan Shao,Xiaofang Feng,Haojie Zeng,Yuchuan Liu,Runxuan Long,Ximei Zhu
In order to effectively solve the two major problems of photocatalyst recovery and membrane fouling , this research combines photocatalyst and membrane separation technology . In this study, the NH 2 -MIL-88B(Fe)/CDs@GO material with good photocatalytic properties was synthesized by hydrothermal method and mechanical stirring, and the photocatalytic membrane was obtained by vacuum filtration. The results show that the NH 2 -MIL-88B(Fe)/CDs@GO membrane can effectively intercept and degrade methylene blue (MB). After 10 cycles, the rejection rate of MB can still reach 99.5%, which is about 2.5 times of pure GO membrane (40%). After 15 min of visible light irradiation, the Flux recovery rate (FRR) of NH 2 -MIL-88B(Fe)/CDs@GO membrane can reach 95%, and the antifouling performance is excellent. In this study, the composite photocatalytic membrane shows excellent stability, photocatalytic performance and self-cleaning property, which is conducive to widening the application prospect of wastewater treatment .
研究领域:
环境科学
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材料科学
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DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2022
·
IF 9.965
Xiaolong Hu,Jingyu Bao,Daiwen Chen,Syed Jalil Shah,Sidra Subhan,Wenxue Gong,Wenyuan Li,Xinqi Luan,Zhongxing Zhao :,Zhenxia Zhao
In the photo-Fenton reactions, fast recombination of photoinduced electrons and holes in Fe-based metal–organic frameworks (Fe-MOFs) slows Fe(III)/Fe(II) cycle, which remains big challenge that significantly retards the overall process. Herein, NH 2 -MIL-88B(Fe) (NM88) was modified with 3,5-diaminobenzoic acid (DB) and TPB-DMTP-COF (COF-OMe) to in situ construct NM88(DB) 0.85 /COF-OMe composite that could strongly harvest the visible light for photo-Fenton degradation of sulfamerazine (SMR). With the addition of DB, electron-donating effect of NM88 was strengthened, which then promoted amino groups to react with aldehyde groups (Schiff-base), and thus highly facilitated the interfacial contact between NM88 and COF-OMe. Such modifications increased the degradation rate constants for NM88(DB) 0.85 /COF-OMe to 15.1 and 17.3 times that of NM88 and COF-OMe respectively with good reusability. Moreover, the catalyst exhibited 32–170 times higher degradation kinetics in comparison to other reported catalysts. Results showed that due to the Schiff-base reaction between NM88(DB) and COF-OMe, electron density on Fe(III) was decreased; and the photogenerated electrons of COF-OMe moved to NM88(DB) to reduce Fe(III), thus resulting in the generation of highly active Fe(II) and ·OH species. Furthermore, the main reactive species were determined to be ·OH and ·O 2 – by trapping experiments, and a possible mechanism of the degradation system followed Z-scheme charge transfer.
研究领域:
环境科学
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材料科学
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DOI
PubMed
高影响因子
INORGANIC CHEMISTRY
·
2021
·
IF 5.165
Dianfa Zhao,Jie Liu,Lijuan Zhang,Yunshan Zhou,Yuxu Zhong,Yang Yang,Chengcheng Huang,Yong’an Wang
Maintaining a long-term continuous and stable reactivator blood concentration to treat organophosphorus nerve agent poisoning using acetylcholinesterase (AChE) reactivator pralidoxime chloride (2-PAM) is very important yet difficult. Because the flexible framework of MIL-88B(Fe) nanoparticles (NPs) can swell in polar solvents, pralidoxime chloride (2-PAM) was loaded in MIL-88B(Fe) NPs (size: ca. 500 nm) by stirring and incubation in deionized water to obtain 2-PAM@MIL-88B(Fe), which had a maximum drug loading capacity of 12.6 wt %. The as-prepared composite was characterized by IR, powder X-ray diffraction (P-XRD), scanning electron microscopy (SEM), ζ-potential, Brunauer–Emmett–Teller (BET), and thermogravimetry/differential thermal analysis (TG/DTA). The results showed that under constant conditions, the maximum drug release rates of 2-PAM@MIL-88B(Fe) in absolute ethanol, phosphate-buffered saline (PBS) solution (pH = 7.4), and PBS solution (pH = 4) at 150 h were 51.7, 80.6, and 67.1%, respectively. This was because the composite showed different swelling behaviors in different solvents. In PBS solution with pH = 2, the 2-PAM@MIL-88B(Fe) framework collapsed after 53 h and released 100% of 2-PAM. For mice after intragastric poisoning with sarin (a neurotoxic agent), an atropine-assisted 2-PAM@MIL-88B(Fe) treatment experiment revealed that 2-PAM@MIL-88B(Fe) continuously released 2-PAM for more than 72 h so that poisoned AChE was continuously and steadily reactivated. The reactivation rate of AChE was 56.7% after 72 h. This composite is expected to provide a prolonged, stable therapeutic drug for the mid- and late-stage treatment of neurotoxic agent poisoning.
研究领域:
药理学
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材料科学
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毒理学
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产品关联
DOI
PubMed
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2024
·
IF 2.7
Ziwei Zhao,Qi Ling,Shangkun Deng,Ziliang Li,Jianguo Lv,Lei Yang,Chunbin Cao,Zhaoqi Sun,Miao Zhang
A type II heterostructured BiVO4/MIL-88B(Fe) composite was successfully synthesised for the photocatalytic degradation of tetracycline hydrochloride (TC-HCl) by a simple hydrothermal method. Thin film materials avoid secondary pollution of powder materials. The samples were characterised by XRD, SEM, TEM, XPS, UV-Vis DRS, and PL. The samples were also characterised for their optoelectronic properties. 3-BV/MIL-88B(Fe) (3 mmol BiVO4) was the most effective catalyst for the degradation of TC-HCl, achieving 92.1% removal at 75 min with a degradation rate constant of 22.79 × 10−3 min−1. Moreover, durability evaluation and TC-HCl degradation potential evaluation were also performed. We looked into how TC-HCl concentration, pH and ions affect the degradation results. In order to determine the active ingredients, experiments for trapping free radicals and EPR tests were performed. The results indicated that the main active species were h+ and ˙OH. It is proposed that a reasonable type-II heterostructure can help to explain the photocatalytic mechanism. The current study creates a stable photocatalytic system by compositing electrocatalytic and photocatalytic materials to achieve efficient antibiotic degradation and provides a viable strategy for future applications.
研究领域:
材料科学
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环境科学
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化学
·
纳米技术
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产品关联
DOI
高影响因子
MICROCHIMICA ACTA
·
2021
·Vol. 188
·期 5
·1-8
·
IF 5.833
Sun Ying,Lin Tianran,Zeng Cuihong,Jiang Gaoyan,Zhang Xuanhan,Ye Fanggui,Zhao Shulin
A self-correcting fluorescent assay of tyrosinase (TYR) was developed by utilization of Fe-MIL-88B-NH 2 as a peroxidase-like nanozyme and a capture probe. Fe-MIL-88B-NH 2 nanozyme was selected as an electron donor, and the oxidization product (dopamine- o -quinone) acts as an energy acceptor. First, TYR catalyzes the oxidation of tyramine hydrochloride to dopamine and then to dopamine- o -quinone. Second, Fe-MIL-88B-NH 2 with intrinsic peroxidase-like activity decomposes H 2 O 2 to produce ·OH radicals, which further accelerate the oxidation of dopamine to dopamine- o -quinone. Excessive H 2 O 2 and ·OH radicals reduce the interferences from ascorbic acid at the same time providing a self-correcting ability. Dopamine- o -quinone reacts with -NH 2 groups on the ligand of Fe-MIL-88B-NH 2 through Michael reaction which results in fluorescence quenching. Under 365-nm excitation, the fluorescence emission intensity at 452 nm gradually decreased with increasing TYR concentration varying from 0 to 10 U mL −1 . The linear range is from 1 to 5 U mL −1 and the detection limit is 0.05679 U mL −1 . This self-correcting fluorescent assay of tyrosinase exhibits good sensitivity and selectivity which is also successfully applied for tyrosinase inhibitor detection. Graphical abstract
Schematic representation of fluorescent assay for tyrosinase determination based on Fe-MIL-88B-NH 2 nanozyme. A self-correcting fluorescent assay for tyrosinase was developed based on the Fe-MIL-88B-NH 2 nanozyme.
研究领域:
分析化学
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生物化学
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纳米技术
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酶学
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产品关联
DOI
PubMed
高影响因子
APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING
·
2021
·Vol. 127
·期 12
·1-11
·
IF 2.584
Fu Manjun,Chai Bo,Yan Juntao,Wang Chunlei,Fan Guozhi,Song Guangsen,Xu Fang
Hydrogen peroxide (H 2 O 2 ) was widely applied as the bactericide and bleach agent in food industry due to its strong oxidation, whose residue had also posed a hazard to public health at the same time. Therefore, it was indispensable to establish a simple, highly effective and accurate method for the detection of H 2 O 2 in foods. Herein, the MIL-88B-Fe metal–organic framework (MOF) was prepared by a facile solvothermal process and utilized as the peroxidase mimic for H 2 O 2 detection. The resultant MIL-88B-Fe MOF exhibited an excellent peroxidase mimetic activity to effectively catalyse the oxidation of 3,3’,5,5’-tetramethylbenzidine (TMB) in the presence of H 2 O 2 , generating a blue coloured product. Under the optimal testing conditions, the linear absorbance response is well correlated with the H 2 O 2 concentration ranging from 10 to 100 μM with a detection limit of 0.60 μM. The catalytic kinetic assay suggested that the MIL-88B-Fe MOF possessed the higher affinity towards both the substrate TMB and H 2 O 2 than horseradish peroxidase. Moreover, the MIL-88B-Fe MOF also displayed a high selectivity and anti-interference performance towards H 2 O 2 detection. In addition, the peroxidase mimetic catalytic oxidation TMB mechanism over the MIL-88B-Fe MOF was clarified by the photoluminescence test. Benefitting from the sensitive response and good anti-interference capacity, this method was applied in real milk and beer samples for H 2 O 2 detection and showed a favourable reproducibility and feasibility. These results indicated that the proposed method based on MIL-88B-Fe as peroxidase mimic might be a promising candidate for H 2 O 2 detection in food field.
研究领域:
食品科学
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生物化学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子