SCIENCE OF THE TOTAL ENVIRONMENT
·
2025
·
IF 8
Yuxin Lin,Luyao Wang,Sining Meng,Jianjia Liu,Xinyu Li,Wenjuan Wang,Miaoyang Hu,Xi Wang,Weixia Duan,Shangcheng Xu,Jun Wang,Rong Gao
Bisphenol F (BPF), one of the major substitutes for bisphenol A (BPA), is increasingly used in pharmaceuticals, food packaging, and chemical manufacturing. Emerging evidence suggests its potential neuropsychiatric risks. However, the underlying mechanisms remain poorly characterized. Thus, the present study was performed to investigate the roles of the kynurenine (KYN) pathway in BPF induced anxiety- and depression-like behaviors, especially the keys roles of the toxic metabolite 3-hydroxykynurenine (3−HK). The mice were administrated with BPF (10, 40, 160 μg/kg/day) for 30 consecutive days, and the behaviors as well as the changes of the KYN pathway were examined. Noteworthily, even low-dose of BPF exposure (40 μg/kg/day) elicited pronounced anxiety- and depression-like behaviors, molecularly shown as the synaptic marker proteins (PSD95, SYN) and dendritic spine proteins (Drebrin) loss in the prefrontal cortex and hippocampus, along with impaired synaptic connection. The UHPLC-MS/MS metabolomic profiling revealed the aberrant metabolism of the KYN pathway, as shown by the elevated neurotoxic metabolite 3-HK and decreased neuroprotective metabolite kynurenic acid (KynA). Mechanistic analyses demonstrated that the 3-HK rate-limiting enzyme KMO was upregulated while the KynA rate-limiting enzyme KAT2 was downregulated in mouse brain. Notably, pharmalogical inhibition of KMO (GSK180) or blockage kynurenine generation with the TDO2 inhibitor (680C91) substantially ameliorated the BPF induced anxiety- and depression-like behaviors and synaptic impairments. Collectively, the present study unravels a previously unrecognized the BPF induced anxiety- and depression-like behaviors in mice via KMO and 3-HK increase. Therefore, targeting the KMO may provide novel interventive strategy for BPF induced neurobehavioral disorders.
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CHEMISTRY & BIODIVERSITY
·
2025
·
IF 2.5
Zhi-Wen Wan,Rui Meng,Hua-Yuan Yang,Xing Yang,Qin Zhou,Min Wu,Bin Li,Xia Zhang
Rosa roxburghii f. eseiosa Ku, a thornless variety of Rosa roxburghii Tratt, remains underexplored regarding the tissue-specific functionality and structure-activity relationships of its polysaccharides. This study systematically investigated the composition and bioactivities of polysaccharides extracted from the fruit, root, stem, and thick stem of this variant. Using gradient ethanol precipitation (40%, 60%, and 80%), polysaccharides with distinct molecular weight (M w ) profiles were obtained. All isolates were identified as acidic heteropolysaccharides with complex and tissue-dependent monosaccharide compositions. Fractions precipitated with 60% and 80% ethanol exhibited lower M w s and significantly enhanced bioactivities, including potent radical scavenging capacity and α -glucosidase inhibition. Notably, RREK-R60, the crude polysaccharide obtained from the roots of Rosa roxburghii f. eseiosa Ku via 60% ethanol precipitation, exhibited a notable α -glucosidase inhibition rate of 92.91%. Structural analysis revealed tissue-specific traits, such as the unique presence of N-acetylglucosamine in fruit and root samples, along with elevated uronic acid, galactose, and arabinose content, which correlated strongly with bioactivity. These findings underscore the potential of Rosa roxburghii f. eseiosa Ku polysaccharides as functional food ingredients or anti-diabetic agents. Further in vivo studies and detailed structural elucidation are warranted to fully establish their structure-activity relationships. Graphical The graphical abstract comprises three sections. The left panel shows the distribution of different tissues of Rosa roxburghii f. eseiosa Ku. The middle illustrates the flowchart for the extraction and purification of crude polysaccharides. The right section presents Key Findings on Bioactive Polysaccharides from Rosa roxburghii f. eseiosa Ku. This figure summarizes the structure-activity relationships of polysaccharides from various tissues of the plant. Major findings include: 1) N-Acetylglucosamine content positively correlates with 2,2-diphenylpicrylhydrazyl radical scavenging activity; 2) Polysaccharides obtained with 60–80% ethanol exhibit superior antioxidant capacity, attributed to lower molecular weight and higher polyphenol content; 3) Higher galactose content in RREK-F60 and RREK-R60 enhances 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) radical scavenging; 4) RREK-R60 shows remarkable α-glucosidase inhibition (92.91%), likely due to its high arabinose, glucose, and xylose composition.
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高影响因子
Journal of Material Cycles and Waste Management
·
2023
·Vol. 25
·期 4
·2485-2497
·
IF 3.1
Wei Jie,Liu Zhanwei,Yan Hengwei,Yang Wanzhang
Herein, fluorine fixation, nitrogen removal, and the alkaline solution recovery of alumina were studied using calcium-based high-temperature soda roasting. In addition, the effects of roasting conditions, dissolution conditions, and additives (carbon alkali and calcium salt) on fluorine fixation and alumina recovery were studied. The results show that when the roasting temperature was 1100 ℃ and the roasting time was 2 h, the dissolution temperature was 80 °C, while the dissolution time was 20 min. The ratio of soda to dross was 1.0, and 30 wt% CaCO 3 had been added as a fluorine fixing agent. The Al extraction rate from aluminum dross (AD) reached 86.21%, the denitrification rate reached 99.54%, the concentration of soluble fluoride ion was reduced to 0.111 g·L −1 , and the fluoride fixation rate was 75.04 wt%. CaF 2 is the main component of the leaching residue, which can be added as an insulation material for electrolysis. Alkaline oxidation roasting and calcium-based fluoride fixation are effective methods to separate aluminum, fluoride, and nitrogen. This study provides a new method for the safe and efficient utilization of AD.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2023
·
IF 7.2
Jin Song,Fenglong Wu,Yulun Lu,Xinyan Zhang
Doping as a common mean to generate defects to boost the catalytic performance of metal oxide semiconductor-based materials has aroused great interest. However, doping usually requires high temperatures and is time consuming. Herein, we report a facile strategy for the preparation of F doped CeO 2 (F–CeO 2 ) with assistance of the electrostatic attraction between F − and CeO 2 with oxygen vacancies at room temperature , then F–CeO 2 acts as superior support of metal Co nanoparticles (NPs) for efficient hydrolysis of NH 3 BH 3 under light irradiation . The activity of Co/F–CeO 2 is significantly enhanced and Co/F–CeO 2 -0.6 exhibited highest catalytic activity with TOF value 92.8 min −1 which increases 47% compared with Co/CeO 2 . Experimental and characterization results show the enhanced performance attributes to high efficiency photogenerated carrier separation and boosting adsorption capacity of H 2 O and NH 3 BH 3 over Co/F–CeO 2 due to F doped into CeO 2 crystallites . Furthermore, theory calculations further confirm that the band gap of F–CeO 2 becomes smaller and F–CeO 2 is more favorable the adsorption for H 2 O and NH 3 BH 3 than pure CeO 2 . This work offers a facile and time efficiency strategy to realize controllable element doped in metal oxide under ambient, and gives deep insights into the structure–activity relationship of catalyst between defect engineering and photocatalytic performance.
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SENSORS AND ACTUATORS B-CHEMICAL
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2014
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IF 3.84
Haiyang Liu,Xuejuan Wan,Tianqi Liu,Yuanqing Li,Youwei Yao
Cascade recognition of trivalent chromium cation (Cr 3+ ) and fluoride anion (F − ) via rhodamine-urea methacrylate-based fluorescent probe (RhBUA) and its subsequent cationic complex was reported. The non-fluorescent rhodamine derivatives can selectively detect Cr 3+ cation over some other metal ions in CH 3 CN–H 2 O (90/10, v/v, pH 7.0) solutions with a 1:1 stoichiometry, leading to prominent fluorescence OFF–ON switching. The obtained RhBUA–Cr 3+ complex can subsequently serve as a sensitive and selective chemosensor for F − ion. Complete signal quenching (fluorescence ON–OFF switching) can also be observed, ascribing to the extraction of Cr 3+ cation and the resulting deformation of RhBUA–Cr 3+ complex.
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Biomaterials Science
·
2020
·Vol. 9
·期 6
·2009-2019
·
IF 6.183
Y. D. Chen,C. Shu,Z. H. Duan,J. J. Xu,X. J. Li,F. Chen,Q. J. Luo,X. D. Li
Dental caries have become a major global public health problem. Plaque control and remineralization of initial enamel lesions are paramount for the prevention and control of caries. Polyhexamethylene biguanide (PHMB) is a type of cationic amphipathic antibacterial agent with broad-spectrum antibacterial properties and good biological safety. Fluoride delays demineralization and promotes the remineralization of hard dental tissues. However, a high concentration is needed for it to function as an antibacterial agent. In order to create a PHMB with the benefits associated with fluoride, we synthesized a fluorine-containing cationic polymer, PHMB-F. Fourier transform-infrared spectroscopy and solid state nuclear magnetic resonance characterization confirmed the successful synthesis of PHMB-F. Antibacterial tests showed that PHMB-F had better antiseptic efficacy for Streptococcus mutans compared with just PHMB. Moreover, positively-charged PHMB-F allows fluoride ions to exist closer to the enamel surface with negative potential, which markedly lowers the ion concentrations in the microenvironment adjacent to hard dental tissues needed to maintain equilibrium. Thus, only low concentrations of PHMB-F are required for enamel remineralization.
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INORGANICA CHIMICA ACTA
·
2021
·
IF 2.545
Wenting Chen,Hua Liang,Xin Wen,Zongchen Li,Hui Xiong,Qiang Tian,Minhao Yan,Yuanzhi Tan,Guy Royal
To explore the effect of sensor structure on anions detection, three new hydrazones P-CN , P-CF 3 and P-NO 2 having different electron-withdraw groups are synthesized. Their anions recognition properties are investigated compared with those of P-OMe , P-H and acylhydrazone B-NO 2 . It shows all non-nitro hydrazones exhibit increasing sensitivity specifically toward CN − in the order of P-OMe < P-H < P-CN < P-CF 3 , indicated by color change from colorless to different shades of blue. Whereas P-NO 2 responds to CN − , F − and H 2 PO 4 − concurrently and its sensitivity to CN − is more than 4 times higher compared with that of the other hydrazones. CN − can be discriminated from F − by P-NO 2 in acetonitrile/water. On the other hand, B-NO 2 has only discernible response to CN − and F − with less sensitivity than P-NO 2 does. Detection details of P-NO 2 to CN − are investigated by titration, anti-interference tests, Job’s plot, HRMS, pH effect assays. The 1 H NMR, IR and reversibility tests demonstrate the deprotonation mechanism. The detection mechanisms of P-NO 2 and B-NO 2 to CN − are compared and demonstrate the reason of their recognition difference. The detection limits of P-NO 2 to CN − , F − and H 2 PO 4 − in acetonitrile are 0.0477 μM, 0.0876 μM and 1.46 μM, respectively. Hence, this work indicates that strong electron-withdraw group in related probes can improve their anion detection ability, meanwhile conjugation effect should be also considered in structure designing.
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高影响因子
MOLECULES
·
2023
·Vol. 28
·期 23
·7894
·
IF 4.6
Jia-Bin Xiong,Yong-Juan Zhou,Shi-Hui Wang,Zhang-Qi Xiong,Zi-Kun Zhang,Shan-Shan Zhang,Chen-Kunlun Zhang,Chao-Fan Xu,Guo-Qun Liu
MOF (metal organic framework) materials have been used as functional materials in a number of fields due to their diverse spatial tunability, which produces rich porous structures with stable and continuous pores and a high specific surface area. A triboelectric nanogenerator can convert trace mechanical energy into electrical energy, and the application of MOF materials to triboelectric nanogenerators has been intensively studied. In this work, we report on two MOFs with similar spatial structures, and the modulation of the end microstructures was achieved using the difference in F content. The output performance of friction power generation increases with the increase in F content, and the obtained polyacidic ligand materials can be used to construct self-powered corrosion protection systems, which can effectively protect metallic materials from corrosion.Keywords:TENG;MOF;corrosion protection;cathodic protection
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2020
·
IF 4.939
Lin An,Xin Han,Yaogang Li,Hongzhi Wang,Chengyi Hou,Qinghong Zhang
Tantalic oxide (Ta 2 O 5 ), as an excellent transition metal oxide photocatalyst , has been extensively studied on fluorination or self-doped for hydrogen production , while there is little research to combine the two modifications. In this work, surface fluorination self-doped Ta 2 O 5 nanoshuttles (FTNSs) photocatalyst is synthesized successfully by a modified one-step hydrothermal method . The test results show the presence of surface fluorine ions , Ta 4+ and oxygen vacancies in the sample. The FTNSs prepared by hydrothermal method under 180 °C for 24 h exhibits the highest hydrogen evolution rate (HER). The HER is 179.2 and 19.78 μmol h −1 g −1 in the absence of any co-catalyst under full-spectrum and simulated solar light, respectively, which is higher than that of the Ta 2 O 5 nanoshuttles without fluoride and the commercial Ta 2 O 5 . The higher HER can attribute to the existence of F, Ta 4+ and oxygen vacancies, which enhance the photogenerated carrier mobility and reduce the recombination.
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高影响因子
FUEL
·
2025
·
IF 7.5
Penglin Kang,Changgui Song,Jinbo Guo,Yuan Lai,Xiangru Li,Leixin Hou,Wenjie Liu,Xiaodong Li
To achieve a synergistic enhancement of both energy output and safety performance in metal powder-based high-energy materials, this study employed coaxial focusing droplet technology to fabricate HMX/TiH 2 /F composite microspheres. The influence of dispersed phase concentration on microsphere morphology and particle size was systematically investigated. HMX/F and HMX/Ti/F microspheres, prepared using the same method, served as control groups for analyzing crystal structure and functional group composition. Results indicated that all three types of microspheres retained their original chemical structures. Performance tests revealed that HMX/TiH 2 /F microspheres achieved a favorable balance between thermal stability and reactivity, with thermal safety significantly improved compared to the control samples. Specifically, its impact sensitivity increased by 8 J and 13 J compared to HMX/F and HMX/Ti/F, respectively; friction sensitivity increased by 164 N and 228 N; and electrostatic accumulation was reduced by 1.46 and 16.40 nC, respectively, demonstrating superior mechanical and electrostatic safety. Combustion and detonation tests further demonstrated that HMX/TiH 2 /F microspheres exhibited the most intense combustion flame. The ignition delay time was reduced by 67.48 ms and 26.20 ms compared to HMX/F and HMX/Ti/F, respectively, and the combustion duration was shortened by 0.51 s and 0.42 s. Meanwhile, HMX/TiH 2 /F composite microspheres still maintained a high energy output, and the measured detonation velocity was 7685.7 m/s, which was 149.99 m/s higher than that of HMX/Ti/F. These findings indicate that the incorporation of TiH 2 facilitates the coordinated optimization of high-energy materials with respect to both safety and energetic performance, demonstrating promising application potential.
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SURFACE & COATINGS TECHNOLOGY
·
2025
·
IF 6.1
Huaiyin Chen,Mingzu Xu,Jinbo Wang,Congxiang Li,Xiaolin Liu,Meihua Wu,Wei Wang,Longmin Liu,Yongzhao Li,Weihe Yu,Yuekun Lai,Weilong Cai
In this work, amphiphilic Janus F-SiO 2 -NH 2 particles were prepared through step-by-step modification of SiO 2 particles inlaid in and released from paraffin microspheres by fluorosilane and aminosilane respectively, and further modified waterborne epoxy (WEP) coating. The morphology, structure, composition, and surface wettability of the prepared particles as well as the mechanical properties and corrosion resistance were investigated. The results indicate that the modified coating gained the improved mechanical properties and anti-corrosion performance. Electrochemical impedance spectroscopy tests show that after immersion in 3.5 wt% NaCl solution for 15 days, the impedance modulus at low frequency of F-SiO 2 -NH 2 modified WEP coating was above 10 6 Ω∙cm 2 , two orders of magnitude higher than that of WEP coating. The amphiphilic Janus F-SiO 2 -NH 2 particles not only improved the interfacial compatibility and penetration resistance through the good dispersibility, hydrophobic groups and cross-linking with epoxy resin matrix, but also oriented adsorbed on steel surface to form protective hydrophobic layers. This work provides a simple design approach for constructing highly corrosion-resistant waterborne coatings, which has a certain promoting effect on the development of environmentally friendly high-performance anti-corrosion coatings.
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高影响因子
ACS Applied Materials & Interfaces
·
2022
·
IF 10.383
Qiang Fu,Lei Lin,Tao Wu,Qinghua Zhang,Xianjie Wang,Lingling Xu,Jun Zhong,Lin Gu,Zhihua Zhang,Ping Xu,Bo Song
Precious metals (Pt, Ir, Ru, and so on) and related compounds usually demonstrate superb catalytic activity for electrochemical hydrogen production. However, scarcity and stability are still challenges for hydrogen evolution reaction, even for single-atomic-site electrocatalysts. Herein, a fluorine (F) doping strategy is proposed to enhance the strong metal–support interaction between the F-doped Ni3N support and the loaded ruthenium (Ru) species. Via synergistically modulating both the Ru loading amount and F doping concentration, outstanding HER activity was achieved in Ru@F–Ni3N with an overpotential (η) of 115 mV at 100 mA cm–2, superior to the benchmark Pt/C (η = 201 mV). Density functional theory simulation in combination with X-ray photoelectron spectra and X-ray absorption spectroscopy characterizations convincingly demonstrate that, with the strongest electronegativity, F doping could effectively stabilize Ru atoms doped in the F–Ni3N substrate and simultaneously reduce the H bonding strength, which accelerated the desorption of H2. These findings provide a facile strategy to modulate both catalytic activities and stabilities of heteroatom-loaded catalytic materials.
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