INORGANIC CHEMISTRY COMMUNICATIONS
·
2026
·
IF 5.4
Mei Wang,Shan Mou,Xiaofang Tian,Meijie Xie,Xinyu Luo,Pei Zhang,Yingjuan Wang,Boyan Zheng,Qingqing Zou,Qianchun Zhang
Sunset yellow (SY) is a widely used artificial food coloring that can pose health risks when consumed in excess. In this study, a fluorescent sensor for the quantitative analysis of SY content in complex foods was reported. Using ammonium fluoride and sorbic acid as precursors, fluorine-doped carbon quantum dots (F-CDs) were synthesized via solvothermal method. The prepared F-CDs were characterized by transmission electron microscopy (TEM), atomic force microscopy (AFM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). The results revealed that F-CDs had a uniform morphology and fluorine-rich structure, with an average particle size of 2.15 nm. In addition, we found that F-CDs exhibited excellent selectivity for SY, mainly due to the fluorescence quenching effect of SY on F-CDs. Therefore, a fluorescent sensor based on F-CDs was constructed with a linear detection range of 0.010–75 μM ( R 2 = 0.997) and a detection limit of 30 nM. The sensor's practical applicability was demonstrated by analyzing of SY in hard candy, tangerine peel sugar, peach jelly, beer, and bread, with recoveries of 92.1%–115% and RSDs of 1.0–4.8%. What's more, the fluorescence detection results were closely related to the HPLC-DAD validation results (relative deviation ≤0.17), highlighting the accuracy of the method. F-CD-based fluorescence detection platforms offer the advantages of simplicity, sensitivity, and reliability, providing a promising tool for routine SY monitoring in food safety applications.
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Small Science
·
2026
·Vol. 6
·期 4
·e202500570
·
IF 7
Rongyan He,Qiuyu Cao,Wenhui Yan,Shuting Xiao,Xiaoying Liang,Yuxiu Ye,Dongting Zhangsun,Sulan Luo
Effective wound management is crucial for improved outcomes through timely, personalized therapies. Current dressing-based treatments lack dynamic regulation and microenvironment modulation, leading to suboptimal healing. Integrating electrical stimulation therapy with electro-controlled drug delivery promotes skin generation, ensures precise dosing, and accelerates healing. Flexible electronic patches are ideal platforms for these synergistic therapies but face challenges: rigid post-manufacture shapes and sizes limit adaptability to diverse wound geometries, and substrate materials struggle to meet both wound-healing and electronic requirements. This study develops a tailorable, transferable flexible electronic patch with a hexagonal modular design, enabling shape/size customization while maintaining electrical continuity. The water-transfer printing (WTP) technique is used to conveniently transfer conductive chondroitin sulfate (CS) hydrogel (as electrodes and drug reservoirs) and silver circuits onto clinical dressings. This method endows clinical dressings with functionality of electro-controlled drug release and electrical stimulation, simultaneously addressing substrate performance limitations of flexible electronic patches. The patch demonstrates uniform electrical signal transmission, precise electro-responsive drug control in CS hydrogels, and adaptability to wounds of different geometries. It retains electrostimulation and electro-controlled drug delivery performance after cutting, significantly promoting wound healing. This study provides a potential approach to support the advancement of flexible electronics research and clinical translation.
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Journal of Environmental Chemical Engineering
·
2026
·Vol. 14
·期 3
·122417
·
IF 7.5
Xianwen Zhu,Jinyue Yang,Runqing Liu,Yingjun Qiao,Zhong Liu,Zhiqiang Qian
To address the need for efficient separation of dyes and salts in textile wastewater, this study developed a novel two-dimensional talc nanofiltration membrane with high selectivity and fouling resistance. The membrane was constructed via vacuum-assisted self-assembly of exfoliated natural talc nanosheets with glycine (Gly) and chitosan (CS). The intercalation of Gly and CS achieved a synergistic functional coupling of “interlayer sieving” and “surface anti-fouling”: the former precisely tuned the spacing of the two-dimensional channels (∼9.20 Å), while the latter effectively smoothed the membrane surface. During dye/salt separation, the membrane exhibited outstanding performance, demonstrating a high rejection rate for Brilliant Blue (BB) dye (99.74%), a high permeation rate for sodium chloride (94.47%), and a water permeability of 60.95 L m −2 h −1 bar −1 . Furthermore, the introduction of trace amounts of CS significantly enhanced the anti-fouling properties of membranes. After ten fouling-cleaning cycles, the flux recovery rate (FRR) reached 80.06%, representing a 10.91% improvement over the unmodified membrane, while structural integrity and separation performance were well-maintained during long-term operation. This study provides a new strategy for designing high-performance dye separation membranes and broadens the application potential of natural clay minerals in wastewater treatment and resource recovery.
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JOURNAL OF CHROMATOGRAPHY A
·
2023
·
IF 4.1
Tong Chen,Shuya Wang,Xufang Zong,Bingxiang Li,Ye Shu,Xinyuan Di,Wanning Zhu,Guangsan Song,Jun Jiang
Periodic mesoporous organosilicas (PMO) hydrophilic microspheres were synthesized by co-condensation of sulfated polysaccharide from Lilum lancifolium Thunb. bridged silane (SLLTPBS) and polyhedral oligomeric silsesquioxane (POSS) as stationary phase (PMO(SLLTP-POSS)) for per aqueous liquid chromatography (PALC), which would overcome the disadvantages of using a large amount of acetonitrile on the hydrophilic interaction liquid chromatography (HILIC) columns. Average particle size of PMO (SLLTP-POSS) microspheres was 4.9 μm, which was suitable for stationary phase. The retention mechanism of the stationary phase in PALC was mainly hydrophobic interactions and also included some ion-exchange interactions and electrostatic interactions. The acid-base resistance was greatly improved compared to the C18 column. The PMO(SLLTP-POSS) column under PALC mode had increased the resolution when separating some hydrophilic compounds such as eight organic acids and eleven sweeteners compared with the C18 column and HILIC column. The new column was more efficient than the HILIC columns. Additionally, a PALC-triple quadrupole mass spectrometry approach for the simultaneous identification of the eleven sweeteners was developed. The averagere coveries of the eleven compounds were 70.20%–91.33% with the relative standard deviation (RSD) range of 1.74% to 4.27%. The results showed good precision and accuracy of the method.
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AICHE JOURNAL
·
2022
·Vol. 69
·期 5
·e17981
·
IF 4.167
Yihao Chen,Jingjing Chen,Chongchong Chen,Xiaoli Wu,Yifan Li,Jie Zhang,Jingtao Wang
Lamellar membranes, especially assembled by microporous framework nanosheets, have excited interest for fast molecular permeation. However, the underlying molecular dissolution behaviors on membrane surface, especially at pore entrances, remain unclear. Here, hierarchical metal–organic framework (MOF) lamellar membranes with 7 nm-thick surface layer and 553 nm-thick support layer are prepared. Hydrophilic (–NH 2 ) or hydrophobic (–CH 3 ) groups are decorated at pore entrances on surface layer to manipulate wettability, while –CH 3 groups on support layer provide comparable, low-resistance paths. We demonstrate that molecular dissolution behaviors are determined by molecule–molecule and molecule–pore interactions, derived from intrinsic parameters of molecule and membrane. Importantly, two dissolution model equations are established: for hydrophobic membrane surface, dissolution activation energy ( E S ) obeys E S = K m ln[( γ L - γ C ) μd 2 ], while turns to E S = K a ln[( γ L - γ C ) δ e μd 2 ] for hydrophilic one. Particularly, hydrophilic pore entrances exert strong interaction with polar molecules, thus compensating the energy consumed by molecule rearrangement, giving fast permeation (>270 L m −2 h −1 bar −1 ).
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JOURNAL OF THE INDIAN CHEMICAL SOCIETY
·
2022
·
IF 0.243
Haijian Liu,Zhenxiang Li,Wei Zhang,Ying Liu,Rongkai Pan,Guofu Huang
Carbon nanodots (CDs) with superior fluorescence performance were obtained by hydrothermal method using tomatoes as raw materials. When the ultraviolet absorption band of tartrazine and the fluorescence spectrum of CDs have complementary overlaps, the fluorescent internal filter effect (IFE) occurred. Furthermore, the degree of quenching of fluorescence intensity of CDs has an excellent linear correlation with tartrazine concentration. And based on this principle, a method for detecting tartrazine was established. As the decrease of fluorescence intensity, tartrazine can be measured in the linear range of 0.1 μM–40 μM. The detection limit is 39 nM, and the recovery rate is 90.7%∼114.5%. The established protocol was also effectively employed to assay tartrazine in beverage samples, indicating that it has great potential for food color analysis.
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MATERIALS & DESIGN
·
2023
·
IF 8.4
Yue Wang,Yancheng Wang,Chenhao Mao,Deqing Mei
Vat photopolymerization is a widely employed additive manufacturing (AM) technique that commonly applying a digital light processing (DLP) light engine to provide a patterned light source. Notably, printing extreme-size structures is challenging, and the selection of printing parameters was currently highly reliant on repeatable trial-and-error experiments. In this work, a theoretical model for curing depth prediction was established by observing the effect of light intensity. A correction factor n was introduced to optimize the relationship among the critical curing energy, exposure time, and light intensity. Forming experiments verified the accuracy of the proposed theoretical curing depth prediction model, and a correction factor n equal to 0.75 was obtained. Optical rheological characterization experiments and Fourier transform infrared spectroscopy (FTIR) supported the quantitative characterization of the DLP printing process while revealing a stepwise transition during photocuring. Finally, a guidance for quick selection of the optimal curing time for 3D structure was obtained and applied to the high-precision microstructure printing process. High-fidelity microneedle arrays with 12 μm details were printed. This method of rapid selection of printing parameters and printing microstructures with high-precision details can potentially be used in the field of 3D bioprinting.
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Biosensors-Basel
·
2022
·Vol. 12
·期 5
·326
·
IF 5.743
Shuwen Cheng,Danyao Tang,Yi Zhang,Libin Xu,Kunping Liu,Kejing Huang,Zhengzhi Yin
A novel electrochemical sensor designed to recognize and detect tartrazine (TZ) was constructed based on a molecularly imprinted polydopamine (MIPDA)-coated nanocomposite of platinum cobalt (PtCo) nanoalloy-functionalized graphene oxide (GO). The nanocomposites were characterized and the TZ electrochemical detection performance of the sensor and various reference electrodes was investigated. Interestingly, the synergistic effect of the strong electrocatalytic activity of the PtCo nanoalloy-decorated GO and the high TZ recognition ability of the imprinted cavities of the MIPDA coating resulted in a large and specific response to TZ. Under the optimized conditions, the sensor displayed linear response ranges of 0.003–0.180 and 0.180–3.950 µM, and its detection limit was 1.1 nM (S/N = 3). The electrochemical sensor displayed high anti-interference ability, good stability, and adequate reproducibility, and was successfully used to detect TZ in spiked food samples. Comparison of important indexes of this sensor with those of previous electrochemical sensors for TZ revealed that this sensor showed improved performance. This surface-imprinted sensor provides an ultrasensitive, highly specific, effective, and low-cost method for TZ determination in foodstuffs.Keywords:platinum cobalt nanoalloy;molecularly imprinted polydopamine;graphene oxide;tartrazine;electrochemical sensor
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ANALYTICA CHIMICA ACTA
·
2022
·
IF 6.911
Mi Sun,Biao Ma,Shuai Yuan,Lifei Xin,Chao Zhao,Hong Liu
In this work, we report on the mercury thermometer-inspired test strip for potentiometric detection of salivary α-amylase (sAA). The test strip contains a reaction chamber and two split channels, which are connected by a curved hydrophobic channel. The detection of sAA is based on sequential two-step reactions with preloaded reagents on the test strip. In the first step, maltose is produced by catalyzing the hydrolysis of starch using sAA in the reaction chamber. In the second step, the test strip is shaken to introduce the reaction mixture to the split channels under the inertia force, similar to the operation of a mercury thermometer. In one split channel, maltose reduces [Fe(CN) 6 ] 3- to [Fe(CN) 6 ] 4- under the alkaline condition, while the reaction hardly occurs in the other split channel with the neutral condition. This leads to a difference in the ratio of [Fe(CN) 6 ] 3- /[Fe(CN) 6 ] 4- between the two channels and therefore a potential difference that can be measured and correlated to sAA concentration. Using this test strip, sAA in the human saliva sample was quantitatively analyzed within 2 min. The application of this technique in the psychological evaluation was also demonstrated.
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CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Jingjing Chen,Zhijie Yuan,Xiaoli Wu,Jingtao Wang,Yongpeng Yang,Wenpeng Li,Zhongyi Jiang
Here, lamellar membranes with hydrophilic/hydrophobic heterostructured nanochannels are constructed by alternately stacking graphene oxide (GO) and reduced graphene oxide (RGO) nanosheets via dual-needle electrostatic atomization. This technology exhibits facile controllability over membrane nanostructure, where the dual-needle device can compel active reactants to contact in confined space. Through subtly designing spraying parameters, GO and RGO nanosheets can be alternately deposited on the substrate to construct heterostructured nanochannels. And we demonstrate that the asymmetric channel wall-molecule interactions can induce molecule stratification for acetonitrile/water mixture, where hydrophilic GO layer exerts strong attraction to acetonitrile, whereas water molecules are pushed to hydrophobic RGO layer. Then, the strong attraction further induces acetonitrile molecules to form orderly aligned aggregates and transfer quickly, while water molecules are randomly distributed and transfer slowly. The pre-determined different transfer rates afford a high acetonitrile permeance of 38.9 L m –2 h −1 bar −1 and separation factor of acetonitrile/water up to 4.8, surpassing that of homostructured lamellar membranes. Furthermore, this stratification and hence separation performance can be enhanced by channel length, acetonitrile amount in feed, operation temperature and pressure. The first discovery of molecule stratification in heterostructured nanochannels facilitates the sustainable development of advanced separation membranes.
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JOURNAL OF MEMBRANE SCIENCE
·
2022
·
IF 10.53
Jingjing Chen,Xiaoli Wu,Chongchong Chen,Yihao Chen,Wenpeng Li,Jingtao Wang
Two-dimensional lamellar membranes featuring well-defined nanochannels hold great promise for efficient organics separation. However, the extensively existed non-selective microdefects within laminate architecture would impair separation efficiency and structure stability of membranes. Herein, defect-free metal-organic framework (MOF) lamellar membrane is facilely constructed by triple-needle electrostatic atomization technology. Specifically, one needle atomizes small-sized Cu-TCPP MOF nanosheets (TCPP = meso-tetra(4-carboxyphenyl)porphyrin) to build lamellar skeleton, and the other two needles meantime atomize Cu 2+ and TCPP to secondary-assemble crystals among nanosheets. In this manner, these non-selective microdefects are subtly sutured by the regenerated crystals with identical chemical components, resulting in a defect-free MOF lamellar membrane with enhanced structural stability. Importantly, this novel secondary-assembly method highly enhances the separation efficiency and meanwhile keeps high organics permeation for MOF membrane, with rejection of 93.8% for Rose Bengal (1.2 nm) and acetone permeance of 86.9 L m −2 h −1 bar −1 . In addition, the multipoint connection between nanosheets and crystals ensures excellent surface shearing and compaction resistance for MOF membrane, permitting high and steady operation performance for over 100 h. This secondary-assembly methodology by one-step process to construct defect-free and steady lamellar membrane provides a new avenue for the development of efficient separation membranes .
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CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Yizhou Chen,Yuting Bai,Lijun Meng,Wenting Zhang,Jingjing Xia,Zhiming Xu,Rui Sun,Yan Lv,Tianxi Liu
Organic solvent nanofiltration (OSN), as an emerging membrane separation technology, holds great potential in pharmaceutical and chemical applications. However, the development of such a promising technology is severely retarded by the trade-off between permeability and selectivity. Herein, we report a novel thin-film nanocomposite (TFN) membrane by incorporating hollow metal-organic frameworks (MOFs) into the metal-phenolic network (MPN) selective layer for highly efficient OSN. This nanocomposite selective layer is fabricated via an aqueous deposition of tannic acid (TA) and Fe II ions with MOFs, during which the MOFs are in-situ etched to a hollow structure. Attributed to the extra transfer channels provided by hollow MOFs, the methanol permeance of the TFN membranes increases to 24.7 L·m -2 ·h -1 ·bar -1 , exhibiting an improvement of 270% compared with the membranes without MOFs (9.1 L·m -2 ·h -1 ·bar -1 ). Meanwhile, the coordination interaction between TA and metal centers in MOFs endows excellent interfacial compatibility between MPN matrix and MOF fillers, guaranteeing a defect-free selective layer and thus high rejection for small organic molecules (>99% for Alcian blue). Furthermore, various MOFs, including ZIF-67, prussian blue (PB), and MIL-53(Al), are also employed to fabricate MPN/MOF nanocomposite membranes, proving the availability and universality of this facial aqueous deposition strategy. Additionally, we also take deep insight into the mechanism of in-situ etching based on the density functional theory (DFT) calculation to pave the way for the fabrication of TFN membranes with other hollow nanofillers. This work provides a sufficient strategy for the design and construction of novel highly efficient OSN nanocomposite membranes with excellent permeability and retention performance.
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