TALANTA
·
2018
·
IF 4.244
Hao Zhang,Chen Nie,Jiahui Wang,Ruifang Guan,Duxia Cao
Organic-inorganic hybrid fluorescent microspheres (OI-FMs) without typical fluorophores were prepared. Fluorescence quantum yield of OI-FMs is up to 70.0% after being heated in an oven at 120 °C (named as OI-FMs-120). Interestingly, OI-FMs-120 shows different detection performances in different solvents. It can be used for qualitative and quantitative detection of Fe 3 + with a detection limit of 37.8 nM in absolute ethanol. While in aqueous solution, it can be applied as an ON-OFF-ON fluorescent probe . Fluorescence of the probe is quenched by Hg 2 + and later recovered by biothiols. The detection limit is as low as 34.9 nM for Hg 2 + , 91.0 nM for Cys, 0.12 μM for Hcy and 0.13 μM for GSH in aqueous medium, respectively.
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PubMed
高影响因子
Journal of Materials Chemistry A
·
2014
·Vol. 3
·期 5
·2120-2127
·
IF 0
Fangyuan Gai,Tianlei Zhou,Yunling Liu,Qisheng Huo
In this study, a water-soluble Fe3+ ratiometric fluorescent sensor was designed and synthesized by encapsulating a donor–acceptor (D–A) dye 4-formacyl-triphenylamine (FTA) into silica cross-linked micellar nanoparticles (SCMNPs). The quenching of FTA-encapsulated SCMNPs (FTA-SCMNPs) on Fe3+ sensing was confirmed using the fluorescence titration method. FTA-encapsulated functionalized SCMNPs (FTA-NH2-SCMNPs and FTA-SO3H-SCMNPs) were synthesized to demonstrate the surface charge effect of nanoparticles on Fe3+ fluorescence sensing. The sensing ability of Fe3+ followed in this order: FTA-SO3H-SCMNPs > FTA-SCMNPs > FTA-NH2-SCMNPs, which indicates that particles with stronger negative charge have better sensing abilities. Moreover, linear correlation between the quenching intensity and lower concentration of Fe3+ was in accordance with the Stern–Volmer equation in FTA-SCMNPs and FTA-SO3H-SCMNPs. FTA-SO3H-SCMNPs showed good selectivity for Fe3+ detection. Because of the charge effect of functionalized SCMNPs on a dye-doped Fe3+ sensing system, these kinds of nanoparticles offered possibilities to construct sensing ability-enhanced fluorescence-quenching sensors by tuning the surface charge.
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DOI
Water
·
2024
·Vol. 16
·期 24
·3658
·
IF 3
Jialin Chen,Yi Xie,Jun Xia,Xiaolin Zhang,Dong Chen
An advanced photochemical reduction system involving the UV/Fe(III)–oxalate system was developed for the reduction of nitrate (NO3−) to harmless N-gaseous species, primarily nitrogen (N2), by carbon dioxide radical (·CO2−) generated in the presence of dissolved oxygen (DO). Electron paramagnetic resonance (EPR) analyses confirmed the presence of both ·CO2−and ·OH radicals. Systematic investigations were conducted on various operational parameters, such as the initial Fe(III) concentration, oxalate concentration, and pH levels, to assess their impacts on the efficiency and products of NO3−reduction. Notably, solution pH played a significant role in influencing the NO3−reduction efficiency and the final products. At pH 2, approximately 75% of NO3−was converted into N2with an 80% selectivity. In the pH range of 3 to 5, a remarkable NO3−removal rate of about 90% was achieved. Furthermore, higher concentrations of Fe(III) (2 mM) and oxalate (10 mM) were found to enhance NO3−removal to 91.95% and 88.71%, respectively. The presence of DO increased the oxidative potential in the reaction system, subsequently enhancing the selectivity conversion of NO3−to N2. In summary, the UV/Fe(III)–oxalate system exhibits significant potential for effective removal of NO3−while achieving high selectivity for the production of N2in water remediation applications.
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高影响因子
MICROCHEMICAL JOURNAL
·
2024
·
IF 4.9
Fang Li,Nuotong Shen,Qingcheng Li,Chen Yang,Limin Zhang,Mingjin Wang
The development of microfluidic flow injection analysis (FIA) system for simultaneous and real-time detection of multiple metal ions is of great importance for environmental monitoring, food safety and industrial field. In this work, a multiplexed microfluidic chip based FIA system was fabricated for simultaneous determination of three metal ions, by using Fe(III), Mn(II) and Cu(II) as models. The multiplexed microfluidic chip based FIA system is composed of three parts, including a multi-channel FIA system for solution manipulation, a group of microfluidic chips for reagents mixing and reaction, and one fiber optic spectrometer for fast and real-time absorbance signal detection. The sample solution and chromogenic reagents were injected into the microfluidic chips to carry out specific colorimetric reactions. Fe(III), Mn(II) and Cu(II) reacts with 5-sulfosalicylic acid, formaldoxime, and bis(cyclohexanone) oxalyldihydrazone, respectively, to generate orange, ember and blue colored solution with peak absorbance at 420 nm, 450 nm, and 600 nm, respectively. The absorbance signal of the generated three channels of solution can be sequentially detected by using only one mini spectrometer. The linear detection range for Fe(III), Mn(II) and Cu(II) is 0.1–20 mg/L, 0.1–12 mg/L and 0.2–12 mg/L, respectively. The limit of detection for Fe(III), Mn(II) and Cu(II) is 0.07, 0.02 and 0.1 mg/L respectively. And the limit of quantification for Fe(III), Mn(II) and Cu(II) is 0.2, 0.07 and 0.3 mg/L, respectively. The recoveries of spiked Fe (III), Mn (II), and Cu (II) in real water samples are between 95.3 % to 106 %. Finally, the developed microfluidic chip based FIA system was successfully applied to simultaneous determination of three metal ions in environmental water samples and zinc smelting solution from zinc hydrometallurgy industry with satisfied results.
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高影响因子
MOLECULES
·
2024
·Vol. 29
·期 17
·4194
·
IF 4.2
Kaiwei Ding,Tingsheng Qiu,Xianhui Qiu,Guanfei Zhao,Qinghao Jiao,Jiangjie Fang,Ruisen Lai,Wenhui Yang
The floatability of fluorite and calcite exhibit similar properties, rendering their flotation separation challenging. Macromolecular polysaccharide reagents containing the polyhydroxyl group have shown broad promising application. The selectivity of polysaccharide is relatively low. In this study, the introduction of Fe3+was employed to enhance the selective adsorption capacity of Pullulan polysaccharide towards fluorite and calcite minerals, thereby achieving effective flotation separation. Furthermore, the mechanism underlying intramolecular interactions was elucidated. The DFT calculation and XPS analysis revealed that the adsorption of Fe3+on the calcite surface was more favorable, leading to the formation of a Ca-O-Fe structure. The MD simulation, XPS analysis, and Zeta potential analysis revealed that the Fe-OH groups on the surface of calcite reacted with the -OH groups in Pullulan and formed bonds, resulting in the formation of a Calcite-Fe-Pullulan structure. This facilitated the attachment of a significant number of Pullulan molecules to the calcite surface. The formation of a hydrophilic layer on the outer surface of calcite by Pullulan, in contrast to the absence of such layer on fluorite’s surface, results in an increased disparity in surface floatability between these two minerals, thereby enhancing the efficiency of flotation separation.
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PubMed
高影响因子
ACS Applied Nano Materials
·
2025
·
IF 5.5
Yue Cao,Xin Zhang,Bo Ren,Xiaodong Yang
Due to the complex physiological and pathological barriers in tumor tissues, the penetration depth of light is limited and the accumulation and distribution of photosensitizers in the tumor are insufficient, which seriously affects the therapeutic effect of photothermal therapy (PTT) on solid tumors. The preparation process of traditional photothermal agents is complicated, and their biosafety needs further improvement. Moreover, photothermal agents are difficult to rapidly excrete from the body after realizing the therapeutic function, which may cause long-term potential harm to the body. In this study, multifunctional nanoparticles (FeCNPs) consisting of iron(III), curcumin, and poly(ethylene glycol) grafted polyglutamate (PLG-g-mPEG) were obtained through a simple one-pot method. The synthesized FeCNPs exhibited an average hydrodynamic size of 125 nm and a polydispersion index (PDI) of 0.462. Furthermore, the nanoparticle has excellent biocompatibility and a photothermal effect. After the PPT, the FeCNPs break down into harmless elements via a dynamic disassembly mechanism triggered by deferoxamine mesylate (DFO), facilitating swift elimination and preventing possible long-term toxicity to major organs. The therapeutic synergies enable efficient tumor removal. In summary, this study demonstrates an approach for the dynamic disassembly of metal-polyphenol nanoparticles, effectively addressing the challenge of balancing the EPR effect and renal clearance.
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高影响因子
Chemical Engineering Journal Advances
·
2021
·
IF 0
Kai Wei,Xiufan Liu,Shiyu Cao,Huijuan Cui,Yu Zhang,Zhihui Ai
In this study, we fabricated a micro-nano structured Fe 2 O 3 @FeB composites by treating commercial Fe 2 O 3 with sodium borohydride. The outside amorphous FeB alloy shell endowed the Fe 2 O 3 @FeB with remarkable Fenton-like performance in organic pollutants oxidation by efficient Fe(III)/Fe(II) cycle. For instance, the pseudo first-order rate constants of RhB degradation using Fe 2 O 3 @FeB as Fenton reagent was 74.6 times that of the Fe 2 O 3 counterpart, the hydroxyl radical generation rate of Fe 2 O 3 @FeB was 1-3 orders of magnitude larger than that of other heterogeneous Fenton reagent. Further mechanistic study unveiled that FeB was oxidized accompanying with Fe(0) and B(0) continuously donated electrons to Fe(III) to secure the efficient generation of surface Fe(II), which could generate additional H 2 O 2 by consecutive single-electron molecular oxygen activation (O 2 →•O 2 − →H 2 O 2 ), leading to enhance •OH production and Fenton-degradation toward typical pollutants. This study provides a facile route for efficient heterogeneous Fenton and strengthens the vital role of molecular oxygen activation on Fenton-like process.
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ELECTROCHIMICA ACTA
·
2021
·
IF 6.901
Fei Miao,Zehao Liu,Xin Kang,Cheng Cheng,Xiaoyu Mao,Ruimeng Li,Heng Lin,Hui Zhang
Heterogeneous catalytic oxidation based on iron species for peroxymonosulfate (PMS) activation is considered as one of the most attractive strategies for wastewater treatment. However, the rate-limiting regeneration of Fe(II) from Fe(III) heavily hampers the efficient activation of PMS. In this study, the introduction of electric field to the Fe-supported bentonite (Fe-B) activated PMS process was proposed to enhance the Fe(III)/Fe(II) redox cycle. The Fe-B catalyst performed well in the removal of Acid Orange 7 (AO7) through the synergistic effect of electrolysis and the continuous redox cycle of Fe(III)/Fe(II) for PMS activation. The use of 0.5 g L −1 Fe-B catalyst and 10 mM PMS yielded nearly complete removal of the AO7 (50 mg L −1 ) in 60 min at 2 mA cm −2 of current density. Based on the results of electron paramagnetic resonance (EPR) spectroscopy, chemical quenching tests, X-ray photoelectron spectroscopy (XPS) analysis, and electrochemical measurements, the decolorization of AO7 was dominantly attributed to surface-bound radicals (SO 4 •− ads and • OH ads ) and also the direct electron transfer at DSA anode. Moreover, the electro/Fe-B/PMS system showed an effective pH range from 2.6 to 9.0 and the abatement of AO7 was slightly affected in the presence of natural background anions. This work provides a feasible strategy of PMS activation by cost-effective Fe-B catalyst coupling with electric field and gives an insight into the accelerated oxidation of recalcitrant pollutants.
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Jingwen Wang,Yu Yang,Lei Chen,Yanping Ding,Linli Tan,Qiulin Shi,Yong Liu,Pengchao Xie
Molybdenum disulfide (MoS 2 ) is viewed as a promising two-dimensional Fenton-like catalyst, but the basal plane could not be well applied in peroxides activation. In this study, Fe(III) species were atomically impregnated on the MoS 2 basal plane to enhance peracetic acid (PAA) activation. The surface Fe(III) up shifted the d-band centre of MoS 2 and acted as electron shuttles in breaking the O-O bonds of PAA. HO • , CH 3 COO • and Fe(V) were generated in the Fe(III)-MoS 2 /PAA system, whereas the 1 O 2 production was inhibited on the Fe(III)-MoS 2 surface. Sulfamethazine (SMT) was efficiently degraded by Fe(III)-MoS 2 /PAA during 15 min reaction, with the observed removal efficiencies of SMT by Fe(III)-MoS 2 ( k obs ) being 25-fold higher than that by MoS 2 . Increasing the dosages of PAA and Fe(III)-MoS 2 facilitated SMT degradation, and high removal rate of SMT was achieved in the pH range of 3–5. HO • and Fe(V) were identified as critical reactive species responsible for the SMT degradation. Nitrification and Smiles rearrangement were proposed as the degradation pathways of SMT based on the identified oxidation products. This study demonstrates that impregnating Fe species would be an effective strategy for strengthening the Fenton-like reactivity of MoS 2 .
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Shuai Yang,Dongqi Tian,Xinhao Wang,Peng Zhou,Zhaokun Xiong,Heng Zhang,Yang Liu,Gang Yao,Bo Lai
Fenton-like technology has been widely used in the field of water treatment as an advanced oxidation processes (AOPs), and a multitude of non-homogeneous catalysts have been reported effectively to enhance it. Herein, nitrogen and sulfur co-doped nanocarbon materials (NSC) was designed and synthesized, which formed a unique mesoporous structure and abundant functional groups on the surface. It exhibits superior catalytic performance to enhance the Fe(III)/H 2 O 2 system for sulfamethoxazole (SMX) degradation, k obs is 18 times higher than Fe(III)/H 2 O 2 system after the introduction of NSC under the same experimental conditions. Also, the working pH of Fe(III)/H 2 O 2 system was broadened by NSC. Quenching and probe experiments demonstrate that hydroxyl radical (∙OH) was the dominant active species. Both dissociative and surface-bound iron species were observed, which indicates direct reduction and in-situ binding of Fe(III), respectively. Further investigation found nitrogen and sulfur co-doped attribute to the formation of abundant functional groups, the C O bond and C S C bond on the surface of NSC result in the directly reduce of Fe(III), while –COOH contributes to the in-situ binding. The intermediates and possible degradation pathway of SMX degradation were proposed based on the results of liquid chromatography-quadrupole time of flight-mass spectrometer (LC-QTOF-MS). The results of cycling and co-existing ions experiments demonstrate that NSC has outstanding potential for application. This work provides a novel insight into the sustained removal of micropollutants from the aqueous environment based on the nanocarbon materials enhancing the Fenton-like oxidation.
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高影响因子
Journal of Materials Chemistry B
·
2014
·Vol. 2
·期 37
·6306-6312
·
IF 0
Fangyuan Gai,Xiang Li,Tianlei Zhou,Xiaogang Zhao,Dongdong Lu,Yunling Liu,Qisheng Huo
This work demonstrates a luminescent chemosensor based on silica cross-linked micellar nanoparticles (SCMNPs) designed by encapsulating a phenothiazine-derived Schiff base, (4E)-4-((10-dodecyl-10H-phenothiazin-7-yl)methyleneamino)-1,2-dihydro-1,5-dimethyl-2-phenylpyrazol-3-one (EDDP), for the selective detection of Fe3+. The encapsulation of EDDP inside SCMNPs (EDDP–SCMNPs) can avoid the metal (Fe3+/Fe2+)-promoted hydrolysis of EDDP and, thus, exhibit highly selective determination of Fe3+. The electron transfer (ET) from EDDP in the core to Fe3+ adsorbed on the shell of EDDP–SCMNPs was verified using UV-vis absorption, fluorescent emission and 3D fluorescence spectra. Moreover, EDDP–SCMNPs showed no sensing ability of Fe2+ due to the weak electron-accepting ability of Fe2+. Significantly, because of their ultrasmall size, nontoxicity, good water solubility and biocompatibility, EDDP-SCMNPs have potential applications in biological systems.
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PubMed
SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Shunlong Pan,Xinrui Guo,Rong Li,Hao Hu,Jingwei Yuan,Biming Liu,Shengqiang Hei,Yongjun Zhang
Advanced oxidation processes (AOPs) have been successfully applied for the degradation of fluoroquinolones, but most studies ignored the removal of fluorine ions (F − ) generated after the degradation, and the remaining F − would cause secondary pollution to the water body. In this study, a novel UV radiation/hydrated Fe(III) oxide (HFO) coupling strategy was utilized to activate peroxymonosulfate (PMS) for the comprehensive enhanced removal of norfloxacin (NX) and the generated F − . Results showed that UV/HFO/PMS process significantly improved NX degradation efficiency compared with individual system, and NX degradation efficiency of 97.3% could be achieved by reactive oxygen species (ROS) generated in the process, in which singlet oxygen ( 1 O 2 ) was the main ROS. Moreover, the remaining concentration of F − was generally below 0.35 mg/L within a wide pH range (4–10). And the simultaneous adsorption of HFO for F − is mainly related to coordination and electrostatic interaction . After five cycles, the catalytic efficiency of HFO for NX removal only dropped by 4.4%. Besides, UV/HFO/PMS system had great anti-interference ability on coexisting anions. UV/vis two-dimensional correlation spectroscopy (2DCOS) analysis revealed that ROS would preferentially degrade the piperazine ring, and the quinolone group would be destroyed before the heteroatom during the degradation of NX. This work provides new insights for the treatment of antibiotic pollution.
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高影响因子
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